WorldWideScience

Sample records for chlorinated organic solvents

  1. Monitoring of the aerobe biodegradation of chlorinated organic solvents by stable isotope analysis

    Science.gov (United States)

    Horváth, Anikó; Futó, István; Palcsu, László

    2014-05-01

    Our chemical-biological basic research aims to eliminate chlorinated environmental contaminants from aquifers around industrial areas in the frame of research program supported by the European Social Fund (TÁMOP-4.2.2.A-11/1/KONV-2012-0043). The most careful and simplest way includes the in situ biodegradation with the help of cultured and compound specific strains. Numerous members of Pseudomonas bacteria are famous about function of bioremediation. They can metabolism the environmental hazardous chemicals like gas oils, dyes, and organic solvents. Our research based on the Pseudomonas putida F1 strain, because its ability to degrade halogenated hydrocarbons such as trichloroethylene. Several methods were investigated to estimate the rate of biodegradation, such as the measurement of the concentration of the pollutant along the contamination pathway, the microcosm's studies or the compound specific stable isotope analysis. In this area in the Transcarpathian basin we are pioneers in the stable isotope monitoring of biodegradation. The main goal is to find stable isotope fractionation factors by stable isotope analysis, which can help us to estimate the rate and effectiveness of the biodegradation. The subsequent research period includes the investigation of the method, testing its feasibility and adaptation in the environment. Last but not least, the research gives an opportunity to identify the producer of the contaminant based on the stable isotope composition of the contaminant.

  2. Scenarios Evaluation Tool for Chlorinated Solvent MNA

    Energy Technology Data Exchange (ETDEWEB)

    Vangelas, Karen; Michael J. Truex; Charles J. Newell; Brian Looney

    2007-02-28

    Over the past three decades, much progress has been made in the remediation of chlorinated solvents from the subsurface. Yet these pervasive contaminants continue to present a significant challenge to the U.S. Department of Energy (DOE), other federal agencies, and other public and private organizations. The physical and chemical properties of chlorinated solvents make it difficult to rapidly reach the low concentrations typically set as regulatory limits. These technical challenges often result in high costs and long remediation time frames. In 2003, the DOE through the Office of Environmental Management funded a science-based technical project that uses the U.S. Environmental Protection Agency's technical protocol (EPA, 1998) and directives (EPA, 1999) on Monitored Natural Attenuation (MNA) as the foundation on which to introduce supporting concepts and new scientific developments that will support remediation of chlorinated solvents based on natural attenuation processes. This project supports the direction in which many site owners want to move to complete the remediation of their site(s), that being to complete the active treatment portion of the remedial effort and transition into MNA. The overarching objective of the effort was to examine environmental remedies that are based on natural processes--remedies such as Monitored Natural Attenuation (MNA) or Enhanced Attenuation (EA). The research program did identify several specific opportunities for advances based on: (1) mass balance as the central framework for attenuation based remedies, (2) scientific advancements and achievements during the past ten years, (3) regulatory and policy development and real-world experience using MNA, and (4) exploration of various ideas for integrating attenuation remedies into a systematic set of ''combined remedies'' for contaminated sites. These opportunities are summarized herein and are addressed in more detail in referenced project documents and

  3. Occupational exposure to chlorinated and petroleum solvents and mycosis fungoides

    DEFF Research Database (Denmark)

    Morales-Suárez-Varela, Maria M; Olsen, Jørn; Villeneuve, Sara;

    2013-01-01

    To evaluate the potential association between occupational exposure to chlorinated and petroleum solvents and mycosis fungoides (MF).......To evaluate the potential association between occupational exposure to chlorinated and petroleum solvents and mycosis fungoides (MF)....

  4. SCENARIOS EVALUATION TOOL FOR CHLORINATED SOLVENT MNA

    Energy Technology Data Exchange (ETDEWEB)

    Vangelas, K; Brian02 Looney, B; Michael J. Truex; Charles J. Newell

    2006-08-16

    Over the past three decades, much progress has been made in the remediation of chlorinated solvents from the subsurface. Yet these pervasive contaminants continue to present a significant challenge to the U.S. Department of Energy (DOE), other federal agencies, and other public and private organizations. The physical and chemical properties of chlorinated solvents make it difficult to rapidly reach the low concentrations typically set as regulatory limits. These technical challenges often result in high costs and long remediation time frames. In 2003, the DOE through the Office of Environmental Management funded a science-based technical project that uses the U.S. Environmental Protection Agency's technical protocol (EPA, 1998) and directives (EPA, 1999) on Monitored Natural Attenuation (MNA) as the foundation on which to introduce supporting concepts and new scientific developments that will support remediation of chlorinated solvents based on natural attenuation processes. This project supports the direction in which many site owners want to move to complete the remediation of their site(s), that being to complete the active treatment portion of the remedial effort and transition into MNA. The overarching objective of the effort was to examine environmental remedies that are based on natural processes--remedies such as Monitored Natural Attenuation (MNA) or Enhanced Attenuation (EA). The research program did identify several specific opportunities for advances based on: (1) mass balance as the central framework for attenuation based remedies, (2) scientific advancements and achievements during the past ten years, (3) regulatory and policy development and real-world experience using MNA, and (4) exploration of various ideas for integrating attenuation remedies into a systematic set of ''combined remedies'' for contaminated sites. These opportunities are summarized herein and are addressed in more detail in referenced project documents and

  5. Biodegradation of Chlorinated Solvents: Reactions near DNAPL and Enzyme Function

    International Nuclear Information System (INIS)

    Chlorinated solvents are among the most widespread groundwater contaminants in the country, contamination which is also among the most difficult and expensive for remediation. These solvents are biodegradable in the absence of oxygen, but this biodegradation requires both a food source for the organisms (electron donor) and the presence of chlorinated solvent biodegrading organisms. These two requirements are present naturally at some contamination sites, leading to natural attenuation of the solvents. If one or both requirements are absent, then engineered bioremediation either through addition of an external electron donor or through bioaugmentation with appropriate microorganisms, or both, may be used for site remediation. The most difficult case for cleanup is when a large residual of undissolved chlorinated solvents are present, residing as dense -non-aqueous-phase- liquid ( DNAPL). A major focus of this study was on the potential for biodegradation of the solvents when pre sent as DNAPL where concentrations are very high and potential for toxicity to microorganisms exist. Another focus was on a better understanding of the biological mechanisms involved in chlorinated solvent biodegradation . These studies were directed towards the chlorinated solvents, trichloroethene (TCE), tetrachloroethene or perchloroethene (PCE), and carbon tetrachloride (CT). The potential for biodegradation of TCE and PCE DNAPL was clearly demonstrated in this research. From column soil studies and batch studies we found there to be a clear advantage in focusing efforts at bioremediation near the DNAPL. Here, chlorinated solvent concentrations are the highest, both because of more favorable reaction kinetics and because such high solvent concentrations are toxic to microorganisms, such as methanogens, which compete with dehalogenators for the electron donor. Additionally, biodegradation near a PCE DNAPL results in an enhanced dissolution rate for the chlorinated solvent, by factors of

  6. Biodegradation of Chlorinated Solvents: Reactions near DNAPL and Enzyme Function

    Energy Technology Data Exchange (ETDEWEB)

    McCarty, P. L.; Spormann, Alfred M.; Criddle, Craig, S.

    2003-12-11

    Chlorinated solvents are among the most widespread groundwater contaminants in the country, contamination which is also among the most difficult and expensive for remediation. These solvents are biodegradable in the absence of oxygen, but this biodegradation requires both a food source for the organisms (electron donor) and the presence of chlorinated solvent biodegrading organisms. These two requirements are present naturally at some contamination sites, leading to natural attenuation of the solvents. If one or both requirements are absent, then engineered bioremediation either through addition of an external electron donor or through bioaugmentation with appropriate microorganisms, or both, may be used for site remediation. The most difficult case for cleanup is when a large residual of undissolved chlorinated solvents are present, residing as dense -non-aqueous-phase- liquid ( DNAPL). A major focus of this study was on the potential for biodegradation of the solvents when pre sent as DNAPL where concentrations are very high and potential for toxicity to microorganisms exist. Another focus was on a better understanding of the biological mechanisms involved in chlorinated solvent biodegradation . These studies were directed towards the chlorinated solvents, trichloroethene (TCE), tetrachloroethene or perchloroethene (PCE), and carbon tetrachloride (CT). The potential for biodegradation of TCE and PCE DNAPL was clearly demonstrated in this research. From column soil studies and batch studies we found there to be a clear advantage in focusing efforts at bioremediation near the DNAPL. Here, chlorinated solvent concentrations are the highest, both because of more favorable reaction kinetics and because such high solvent concentrations are toxic to microorganisms, such as methanogens, which compete with dehalogenators for the electron donor. Additionally, biodegradation near a PCE DNAPL results in an enhanced dissolution rate for the chlorinated solvent, by factors of

  7. Organic Solvent Tropical Report

    International Nuclear Information System (INIS)

    This report provides the basis for closing the organic solvent safety issue. Sufficient information is presented to conclude that risk posed by an unmitigated organic solvent fire is within risk evaluation guidelines

  8. Challenges in subsurface in situ remediation of chlorinated solvents

    OpenAIRE

    Broholm, Mette Martina; Fjordbøge, Annika Sidelmann; Christiansen, Camilla Maymann; Hønning, J.; B. H. Hansen; Nedergaard, L. W.; Kern, Kristina; Uthuppu, Basil; Jakobsen, Mogens Havsteen; Kjeldsen, Peter; Bjerg, Poul Løgstrup; Ottesen, L.

    2014-01-01

    Chlorinated solvent source zones in the subsurface pose a continuous threat to groundwater quality at many sites worldwide. In situ remediation of these sites is particularly challenging in heterogeneous fractured media and where the solvents are present as DNAPL. In situ remediation by chemical as well as biological degradation of chlorinated solvents is a contact sport and requires direct contact between the contaminant and the reactants and/or degrading microorganisms. In fractured geologi...

  9. MICROEMULSION OF MIXED CHLORINATED SOLVENTS USING FOOD GRADE (EDIBLE) SURFACTANTS

    Science.gov (United States)

    Ground water contamination frequently consists of mixed chlorinated solvents [e.g., tetrachloroethylene (PCE), trichloroethylene (TCE), and trans-1,2- dichloroethylene (DCE)]. In this research, mixtures of the food grade (edible) surfactants bis(2-ethylhexyl) sodium sulfosuccinat...

  10. In situ bioremediation of chlorinated solvent with natural gas

    International Nuclear Information System (INIS)

    A bioremediation system for the removal of chlorinated solvents from ground water and sediments is described. The system involves the the in-situ injection of natural gas (as a microbial nutrient) through an innovative configuration of horizontal wells

  11. Assessing the Impact of Chlorinated-Solvent Sites on Metropolitan Groundwater Resources

    OpenAIRE

    Brusseau, Mark L.; Narter, Matthew

    2013-01-01

    Chlorinated-solvent compounds are among the most common groundwater contaminants in the U.S.A. The majority of the many sites contaminated by chlorinated-solvent compounds are located in metropolitan areas, and most such areas have one or more chlorinated-solvent contaminated sites. Thus, contamination of groundwater by chlorinated-solvent compounds may pose a potential risk to the sustainability of potable water supplies for many metropolitan areas. The impact of chlorinated-solvent sites on...

  12. Chlorinated solvent replacements recycle/recovery review report

    Energy Technology Data Exchange (ETDEWEB)

    Beal, M.; Hsu, D.; McAtee, R.E.; Weidner, J.R. (EG and G Idaho, Inc., Idaho Falls, ID (United States)); Berg, L.; McCandless, F.P.; Waltari, S.; Peterson, C. (Montana State Univ., Bozeman, MT (United States). Dept. of Chemical Engineering)

    1992-08-01

    This report is a literature review of waste solvents recycle/recovery methods and shows the results of solvent separations using membrane and distillation technologies. The experimental solvent recovery methods were conducted on solvent replacements for chlorinated solvents at Montana State University. The literature review covers waste solvents separation using distillation, membranes decantation, filtration, carbon adsorption, solvent extraction, and other vapor-phase separation techniques. The results of this study identify solvent distillation methods as the most common separation technique. The alternative separation methods typically supplement distillation. The study shows the need for industries to identify waste solvent disposal methods and investigate the economics of waste solvent recycling as a possible waste reduction method.

  13. Degradation of chlorinated organic solvents in aqueous percarbonate system using zeolite supported nano zero valent iron (Z-nZVI) composite.

    Science.gov (United States)

    Danish, Muhammad; Gu, Xiaogang; Lu, Shuguang; Naqvi, Muhammad

    2016-07-01

    Chlorinated organic solvents (COSs) are extensively detected in contaminated soil and groundwater that pose long-term threats to human life and environment. In order to degrade COSs effectively, a novel catalytic composite of natural zeolite-supported nano zero valent iron (Z-nZVI) was synthesized in this study. The performance of Z-nZVI-catalyzed sodium percarbonate (SPC) in a heterogeneous Fenton-like system was investigated for the degradation of COSs such as 1,1,1-trichloroethane (1,1,1-TCA) and trichloroethylene (TCE). The surface characteristics and morphology of the Z-nZVI composite were tested using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Total pore volume, specific surface area, and pore size of the natural zeolite and the Z-nZVI composite were measured using Brunauer-Emmett-Teller (BET) method. SEM and TEM analysis showed significant elimination of aggregation and well dispersion of iron nano particles on the framework of natural zeolite. The BET N2 measurement analysis indicated that the surface area of the Z-nZVI composite was 72.3 m(2)/g, much larger than that of the natural zeolite (0.61 m(2)/g). For the contaminant analysis, the samples were extracted with n-hexane and analyzed through gas chromatograph. The degradation of 1,1,1-TCA and TCE in the Z-nZVI-catalyzed percarbonate system were 48 and 39 % respectively, while strong augmentation was observed up to 83 and 99 %, respectively, by adding the reducing agent (RA), hydroxyl amine (NH2OH•HCl). Probe tests validated the presence of OH(●) and O2 (●-) which were responsible for 1,1,1-TCA and TCE degradation, whereas both free radicals were strengthened with the addition of RA. In conclusion, the Z-nZVI/SPC oxidation with reducing agent shows potential technique for degradation of groundwater contaminated by 1,1,1-TCA and TCE. PMID:27023817

  14. Production of hydrogen by Clostridium species in the presence of chlorinated solvents.

    Science.gov (United States)

    Bowman, Kimberly S; Rainey, Fred A; Moe, William M

    2009-01-01

    Although anaerobic bioremediation of chlorinated organic contaminants in the environment often requires exogenous supply of hydrogen as an electron donor, little is known about the ability of hydrogen-producing bacteria to grow in the presence of chlorinated solvents. In this study, 18 Clostridium strains including nine uncharacterized isolates originating from chlorinated solvent contaminated groundwater were tested to determine their ability to fermentatively produce hydrogen in the presence of three common chlorinated aliphatic groundwater contaminants: 1,2-dichloroethane (DCA), 1,1,2-trichloroethane (TCA), and tetrachloroethene (PCE). All strains produced hydrogen in the presence of at least 7.4 mM DCA, 2.4 mM TCA, and 0.31 mM PCE. Some strains produced hydrogen in media containing concentrations as high as 29.7 mM DCA, 9.8 mM TCA, and 1.1 mM PCE. None of the strains biotransformed chlorinated solvents under the conditions tested. Results demonstrate that many Clostridium species are chlorinated solvent tolerant, producing hydrogen even in the presence of high concentrations of DCA, TCA, and PCE. These findings have important implications for bioremediation of contaminated soil and groundwater.

  15. In situ aerobic cometabolism of chlorinated solvents: a review.

    Science.gov (United States)

    Frascari, Dario; Zanaroli, Giulio; Danko, Anthony S

    2015-01-01

    The possible approaches for in situ aerobic cometabolism of aquifers and vadose zones contaminated by chlorinated solvents are critically evaluated. Bioaugmentation of resting-cells previously grown in a fermenter and in-well addition of oxygen and growth substrate appear to be the most promising approaches for aquifer bioremediation. Other solutions involving the sparging of air lead to satisfactory pollutant removals, but must be integrated by the extraction and subsequent treatment of vapors to avoid the dispersion of volatile chlorinated solvents in the atmosphere. Cometabolic bioventing is the only possible approach for the aerobic cometabolic bioremediation of the vadose zone. The examined studies indicate that in situ aerobic cometabolism leads to the biodegradation of a wide range of chlorinated solvents within remediation times that vary between 1 and 17 months. Numerous studies include a simulation of the experimental field data. The modeling of the process attained a high reliability, and represents a crucial tool for the elaboration of field data obtained in pilot tests and for the design of the full-scale systems. Further research is needed to attain higher concentrations of chlorinated solvent degrading microbes and more reliable cost estimates. Lastly, a procedure for the design of full-scale in situ aerobic cometabolic bioremediation processes is proposed. PMID:25306537

  16. In situ aerobic cometabolism of chlorinated solvents: a review.

    Science.gov (United States)

    Frascari, Dario; Zanaroli, Giulio; Danko, Anthony S

    2015-01-01

    The possible approaches for in situ aerobic cometabolism of aquifers and vadose zones contaminated by chlorinated solvents are critically evaluated. Bioaugmentation of resting-cells previously grown in a fermenter and in-well addition of oxygen and growth substrate appear to be the most promising approaches for aquifer bioremediation. Other solutions involving the sparging of air lead to satisfactory pollutant removals, but must be integrated by the extraction and subsequent treatment of vapors to avoid the dispersion of volatile chlorinated solvents in the atmosphere. Cometabolic bioventing is the only possible approach for the aerobic cometabolic bioremediation of the vadose zone. The examined studies indicate that in situ aerobic cometabolism leads to the biodegradation of a wide range of chlorinated solvents within remediation times that vary between 1 and 17 months. Numerous studies include a simulation of the experimental field data. The modeling of the process attained a high reliability, and represents a crucial tool for the elaboration of field data obtained in pilot tests and for the design of the full-scale systems. Further research is needed to attain higher concentrations of chlorinated solvent degrading microbes and more reliable cost estimates. Lastly, a procedure for the design of full-scale in situ aerobic cometabolic bioremediation processes is proposed.

  17. Ultrasonic aqueous cleaning as a replacement for chlorinated solvent cleaning

    International Nuclear Information System (INIS)

    The Oak Ridge Y-12 Plant has been involved in the replacement of chlorinated solvents since 1982. One of the most successful replacement efforts has been the substitution of vapor degreasers or soak tanks using chlorinated solvents with ultrasonic cleaning using aqueous detergents. Recently, funding was obtained from the Department of Energy Office (DOE) of Technology Development to demonstrate this technology. A unit has been procured and installed in the vacuum pump shop area to replace the use of a solvent soak tank. Initially, the solvents used in the shop were CFC-113 and a commercial brand cleaner which contained both perchloroethylene and methylene chloride. While the ultrasonic unit was being procured, a terpene-based solvent was used. Generally, parts were soaked overnight in order to soften baked-on vanish. Many times, wire brushing was used to help remove remaining contamination. Initial testing with the ultrasonic cleaner indicated cleaning times of 20 min were as effective as the overnight solvent soaks in removing contamination. Wire brushing was also not required following the ultrasonic cleaning as was sometimes required with the solvent soak

  18. Enhanced reductive dechlorination in clay till contaminated with chlorinated solvents

    DEFF Research Database (Denmark)

    Damgaard, Ida

    Chlorinated solvents are among the most frequently found contaminants in groundwater. In fractured media, chlorinated ethenes and ethanes are transported downwards through preferential pathways with subsequent diffusion into the sediment matrix. Due to slow back diffusion it can serve as a long...... the potential for development of degradation throughout the entire clay matrix. When ERD is applied in a low permeability settings one of the major constraints is to obtain the necessary contact between electron donor, bacteria and contaminants to achieve reasonable remediation timeframes. Two injection methods...

  19. Organic solvent topical report

    Energy Technology Data Exchange (ETDEWEB)

    Cowley, W.L.

    1998-04-30

    This report is the technical basis for the accident and consequence analyses used in the Hanford Tank Farms Basis for Interim Operation. The report also contains the scientific and engineering information and reference material needed to understand the organic solvent safety issue. This report includes comments received from the Chemical Reactions Subcommittee of the Tank Advisory Panel.

  20. Organic solvent topical report

    International Nuclear Information System (INIS)

    This report is the technical basis for the accident and consequence analyses used in the Hanford Tank Farms Basis for Interim Operation. The report also contains the scientific and engineering information and reference material needed to understand the organic solvent safety issue. This report includes comments received from the Chemical Reactions Subcommittee of the Tank Advisory Panel

  1. Organic solvent topical report

    Energy Technology Data Exchange (ETDEWEB)

    COWLEY, W.L.

    1999-05-13

    This report provides the basis for closing the organic solvent safety issue. Sufficient information is presented to conclude that risk posed by an organic solvent fire is within risk evaluation guidelines. This report updates information contained in Analysis of Consequences of Postulated Solvent Fires in Hanford Site Waste Tanks. WHC-SD-WM-CN-032. Rev. 0A (Cowley et al. 1996). However, this document will not replace Cowley et al (1996) as the primary reference for the Basis for Interim Operation (BIO) until the recently submitted BIO amendment (Hanson 1999) is approved by the US Department of Energy. This conclusion depends on the use of controls for preventing vehicle fuel fires and for limiting the use of flame cutting in areas where hot metal can fall on the waste surface.The required controls are given in the Tank Waste Remediation System Technical Safety Requirements (Noorani 1997b). This is a significant change from the conclusions presented in Revision 0 of this report. Revision 0 of this calcnote concluded that some organic solvent fire scenarios exceeded risk evaluation guidelines, even with controls imposed.

  2. Organic solvent topical report

    International Nuclear Information System (INIS)

    This report provides the basis for closing the organic solvent safety issue. Sufficient information is presented to conclude that risk posed by an organic solvent fire is within risk evaluation guidelines. This report updates information contained in Analysis of Consequences of Postulated Solvent Fires in Hanford Site Waste Tanks. WHC-SD-WM-CN-032. Rev. 0A (Cowley et al. 1996). However, this document will not replace Cowley et al (1996) as the primary reference for the Basis for Interim Operation (BIO) until the recently submitted BIO amendment (Hanson 1999) is approved by the US Department of Energy. This conclusion depends on the use of controls for preventing vehicle fuel fires and for limiting the use of flame cutting in areas where hot metal can fall on the waste surface.The required controls are given in the Tank Waste Remediation System Technical Safety Requirements (Noorani 1997b). This is a significant change from the conclusions presented in Revision 0 of this report. Revision 0 of this calcnote concluded that some organic solvent fire scenarios exceeded risk evaluation guidelines, even with controls imposed

  3. Oak Ridge K-25 Site chlorinated solvent pollution prevention opportunity assessment

    International Nuclear Information System (INIS)

    A pollution prevention opportunity assessment (PPOA) was conducted at the Oak Ridge K-25 Site to identify opportunities to reduce and better manage the use of chlorinated solvents. At the K-25 Site, 67 control areas were examined for their potential use of chlorinated solvents. Of these areas, 27 were found to be using (1) chlorinated solvents for cleaning, degreasing, and lubricating; (2) laboratory standards and solvents; and (3) test medium. Current management practices encourage the identification and use of nonhazardous chemicals, including the use of chlorinated solvents. The main pollution prevention principles are source reduction and recycling, and a number of pollution prevention options based on these principles were identified and evaluated as part of this chlorinated solvent PPOA. Source reduction options evaluated for the K-25 Site include the substitution of chlorinated solvents with nonchlorinated solvents. Recycling was identified for those areas that would benefit most from the reuse of the chlorinated solvents in use. The pollution prevention options that offer the greatest opportunity for success at the K-25 Site are the implementation of substitutes at the 10 control areas using chlorinated solvents for cleaning, degreasing, and lubrication. A change in the process may be all that is needed to eliminate the use of a chlorinated solvent. Once a decision is made to implement a substitution, the information should be communicated to all shops and laboratories. Another option to consider is the installation of recycling units to recycle the large amounts of methylene chloride used in the analytical sampling procedure

  4. Biodegradation of chlorinated solvents in a water unsaturated topsoil

    DEFF Research Database (Denmark)

    Borch, T.; Ambus, P.; Laturnus, F.;

    2003-01-01

    In order to investigate topsoils as potential sinks for chlorinated solvents from the atmosphere, the degradation of trichloromethane (CHCl3), 1,1,1-trichloroethane (CH3CCl3), tetrachloromethane (CCl4), trichloroethene (C2HCl3) and tetrachloroethene (C2Cl4) was studied in anoxic laboratory experi...... after 16 days. Based on the results in this study, we conclude that anaerobic topsoils are potential sinks for these contaminants, and that a natural attenuation potential exists, even in water unsaturated topsoils. (C) 2003 Elsevier Science Ltd. All rights reserved....... experiments designed to simulate denitrifying conditions in water unsanstrated by measuring the release of N-15 in N-2 to the headspace from added N-15 labeled nitrate. The degradation of chlorinated aliphatic compounds was followed by measuring their concentrations in the headspace above the soil...

  5. Two-phase ozonation of chlorinated organics

    International Nuclear Information System (INIS)

    In the last few years the amount of research being conducted in the field of single-phase ozonation has grown extensively. However, traditional aqueous-phase ozonation systems are limited by a lack of selective oxidation potential, low ozone solubility in water, and slow intermediate decomposition rates. Furthermore, ozone may decompose before it can be utilized for pollutant destruction since ozone can be highly unstable in aqueous solutions. Naturally occurring compounds such as NaHCO3 also affect ozone reactions by inhibiting the formation of OH-free radicals. To compensate for these factors, excess ozone is typically supplied to a reactor. Since ozone generation requires considerable electric power consumption (16 - 24 kWh/kg of O3), attempts to enhance the ozone utilization rate and stability should lead to more efficient application of this process to hazardous waste treatment. To improve the process, ozonation may be more efficiently carried out in a two-phase system consisting of an inert solvent (saturated with O3) contacted with an aqueous phase containing pollutants. The non-aqueous phase must meet the following criteria: (1) non-toxic, (2) very low vapor pressure, (3) high density (for ease of separation), (4) complete insolubility in water, (5) reusability, (6) selective pollutant extractability, (7) high oxidant solubility, and (8) extended O3 stability. Previously published studies (1) have indicated that a number of fluorinated hydrocarbon compounds fit these criteria. For this project, FC40 (a product of 3M Co.) was chosen due to its low vapor pressure (3 mm Hg) and high specific gravity (1.9). The primary advantages of the FC40 solvent are that it is non-toxic, reusable, has an ozone solubility 10 times that of water, and that 85 % of the ozone remains in the solvent even after 2 hours. This novel two-phase process has been utilized to study the rapid destruction of organic chlorine compounds and organic mixtures

  6. Chlorination of organic material in different soil types

    OpenAIRE

    Gustavsson, Malin

    2009-01-01

    Research has shown that formation of chlorinated organic matter occurs naturally and that organic chlorine is as abundant as the chloride ion in organic soils. A large number of organisms are known to convert inorganic chloride (Clin) to organic chlorine (Clorg) (e.g. bacteria, lichen, fungi and algae) and some enzymes associated to these organisms are capable of chlorinating soil organic matter. The aim with the study was to compare organic matter chlorination rates in soils from several dif...

  7. Molten salt destruction of rubber and chlorinated solvents

    International Nuclear Information System (INIS)

    Acceptable methods for the treatment of mixed wastes are not currently available. The authors have investigated Molten Salt Destruction (MSD) as an alternative to incineration of mixed wastes. MSD differs from incineration in several ways: there is no evidence of open flames in MSD, the containment of actinides is accomplished by chemical means (wetting and dissolution), the operating temperature of MSD is much lower (700--590 C vs 1,000--1,200 C) thus lowering the volatility of actinides. Furthermore, no acid gases are released from MSD. These advantages provide the main incentive for developing MSD as an alternative to incineration. The authors have demonstrated the viability of the MSD process to cleanly destroy rubber and chlorinated solvents

  8. Bioremediation of a Large Chlorinated Solvent Plume, Dover AFB, DE

    Energy Technology Data Exchange (ETDEWEB)

    Bloom, Aleisa C [ORNL

    2015-01-01

    Bioremediation of a Large Chlorinated Solvent Plume, Dover AFB, DE Aleisa Bloom, (Oak Ridge National Laboratory, Oak Ridge, Tennessee, USA) Robert Lyon (bob.lyon@aecom.com), Laurie Stenberg, and Holly Brown (AECOM, Germantown, Maryland, USA) ABSTRACT: Past disposal practices at Dover Air Force Base (AFB), Delaware, created a large solvent plume called Area 6 (about 1 mile long, 2,000 feet wide, and 345 acres). The main contaminants are PCE, TCE, and their degradation products. The remedy is in-situ accelerated anaerobic bioremediation (AAB). AAB started in 2006 and is focusing on source areas and downgradient plume cores. Direct-push injections occurred in source areas where contamination is typically between 5 and 20 feet below ground surface. Lower concentration dissolved-phased contamination is present downgradient at 35 and 50 feet below ground surface. Here, permanent injection/extraction wells installed in transects perpendicular to the flow of groundwater are used to apply AAB. The AAB substrate is a mix of sodium lactate, emulsified vegetable oil, and nutrients. After eight years, dissolved contaminant mass within the main 80-acre treatment area has been reduced by over 98 percent. This successful application of AAB has stopped the flux of contaminants to the more distal portions of the plume. While more time is needed for effects to be seen in the distal plume, AAB injections will soon cease, and the remedy will transition to natural attenuation. INTRODUCTION Oak Ridge National Laboratory Environmental Science Division (ORNL) and AECOM (formerly URS Corporation) have successfully implemented in situ accelerated anaerobic bioremediation (AAB) to remediate chlorinated solvent contamination in a large, multi-sourced groundwater plume at Dover Air Force Base (AFB). AAB has resulted in significant reductions of dissolved phase chlorinated solvent concentrations. This plume, called Area 6, was originally over 1 mile in length and over 2,000 feet wide (Figure 1

  9. Photocatalytic destruction of chlorinated solvents with solar energy

    Energy Technology Data Exchange (ETDEWEB)

    Pacheco, J.; Prairie, M.; Yellowhorse, L.

    1990-01-01

    Sandia National Laboratories and the Solar Energy Research Institute are developing a photocatalytic process to destroy organic contaminants in water. Tests with common water pollutants are being conducted at Sandia's Solar Thermal Test Facility using a near commercial-scale single-axis tracking parabolic trough system with glass pipe mounted at its focus. Experiments at this scale provide verification of laboratory studies and allow examination of design and operation issues at a real-life scale. The catalyst, titanium dioxide (TiO{sub 2}), is a harmless material found in paint, cosmetics and toothpaste. Experiments were conducted to determine the effect of key process parameters on destruction rates of two chlorinated organic compounds which are common water pollutants: trichloroethylene and trichloroethane. In this paper, we summarize the engineering-scale results of these experiments and analyses. 21 refs., 8 figs.

  10. Chlorinated organic compounds in urban river sediments

    Energy Technology Data Exchange (ETDEWEB)

    Soma, Y.; Shiraishi, H.; Inaba, K. [National Inst. of Environmental Studies, Tsukuba, Ibaraki (Japan)

    1995-12-31

    Among anthropogenic chemicals, many chlorinated organic compounds have been used as insecticides and detected frequently as contaminants in urban river sediments so far. However, the number and total amount of chemicals produced commercially and used are increasing year by year, though each amount of chemicals is not so high. New types of contaminants in the environment may be detected by the use of newly developed chemicals. Chlorinated organic compounds in the urban river sediments around Tokyo and Kyoto, large cities in Japan, were surveyed and recent trends of contaminants were studied. Contaminants of the river sediments in industrial areas had a variety, but PCB (polychlorinated biphenyls) was detected in common in industrial areas. Concentration of PCB related well to the number of factories on both sides of rivers, although the use of PCB was stopped 20 years ago. In domestic areas, Triclosan (5-chloro-2-(2,4-dichlorophenoxy)-phenol) and Triclocarban (3,4,4{prime}-trichlorocarbanilide)(both are contained in soap or shampoo for fungicides), p-dichlorobenzene (insecticides for wears) and TCEP(tris-chloroethyl phosphate) were detected. EOX(extracted organic halogen) in the sediments was 5 to 10 times of chlorinated organic compounds detected by GC/MS. Major part of organic halogen was suggested to be included in chlorinated organics formed by bleaching or sterilization.

  11. BIOVENTING OF CHLORINATED SOLVENTS FOR GROUND-WATER CLEANUP THROUGH BIOREMEDIATION

    Science.gov (United States)

    Chlorinated solvents such as tetrachloroethylene, trichloroethylene, carbon tetrachloride, chloroform, 1,2-dichloroethane, and dichloromethane (methylene chloride) can exist in contaminated subsurface material as (1) the neat oil, (2) a component of a mixed oily waste, (3) a solu...

  12. Insights and Modelling Tools for Designing and Improving Chlorinated Solvent Bioremediation Applications

    OpenAIRE

    Robinson, Clare; Gerhard, Jason I.; Brovelli, Alessandro; Kouznetsova, Irina; Kokkinaki, Amalia; Brent E. Sleep; Bartlett, Craig; Barry, David Andrew

    2010-01-01

    The chlorinated solvents tetrachloroethene (PCE) and trichloroethene (TCE) have been used extensively in industry and are now amongst the most common and hazardous groundwater contaminants. These solvents are typically present as dense, non-aqueous phase liquids (DNAPLs) and represent long-term source zones that produce persistent contamination plumes in aquifers. Under anaerobic conditions, chlorinated ethenes may be biodegraded via reductive dechlorination (the biologically mediated, step-w...

  13. Multiple sclerosis and organic solvents

    DEFF Research Database (Denmark)

    Mortensen, J T; Brønnum-Hansen, Henrik; Rasmussen, K

    1998-01-01

    We investigated a possible causal relation between exposure to organic solvents in Danish workers (housepainters, typographers/printers, carpenters/cabinetmakers) and onset of multiple sclerosis. Data on men included in the Danish Multiple Sclerosis Register (3,241 men) were linked with data from......, and butchers. Over a follow-up period of 20 years, we observed no increase in the incidence of multiple sclerosis among men presumed to be exposed to organic solvents. It was not possible to obtain data on potential confounders, and the study design has some potential for selection bias. Nevertheless......, the study does not support existing hypotheses regarding an association between occupational exposure to organic solvents and multiple sclerosis....

  14. Field-usable portable analyzer for chlorinated organic compounds

    International Nuclear Information System (INIS)

    In 1992, a chemical sensor was developed which showed almost perfect selectivity to vapors of chlorinated solvents. When interfaced to an instrument, a chemical analyzer will be produced that has near- absolute selectivity to vapors of volatile chlorinated organic compounds. TRI has just completed the second of a 2-phase program to develop this new instrument system, which is called the RCL MONITOR. In Phase II, this instrument was deployed in 5 EM40 operations. Phase II applications covered clean-up process monitoring, environmental modeling, routine monitoring, health and safety, and technology validation. Vapor levels between 0 and 100 ppM can be determined in 90 s with a lower detection limit of 0.5 ppM using the hand-portable instrument. Based on the favorable performance of the RCL MONITOR, the commercial instrument was released for commercial sales on Sept. 20, 1996

  15. Nanopapers for organic solvent nanofiltration.

    OpenAIRE

    Mautner, A.; Lee, K Y; P. Lahtinen; Hakalahti, M.; Tammelin, T. (Tuija); Li, K.; Bismarck, A.

    2014-01-01

    Would it not be nice to have an organic solvent nanofiltration membrane made from renewable resources that can be manufactured as simply as producing paper? Here the production of nanofiltration membranes made from nanocellulose by applying a papermaking process is demonstrated. Manufacture of the nanopapers was enabled by inducing flocculation of nanofibrils upon addition of trivalent ions.

  16. Reduction of chlorinated solvents at the Y-12 Oak Ridge Plant

    Energy Technology Data Exchange (ETDEWEB)

    Thompson, L.M.; Simandl, R.F.; Richards, H.L. [Oak Ridge Y-12 Plant, TN (United States)

    1989-11-01

    The Oak Ridge Y-12 Plant has been actively seeking replacements for chlorinated solvents for several years. The first step in the reduction program was the identification of the solvents and their usages. The four main solvents used at the plant include Freon, methyl chloroform, perchloroethylene, and methylene chloride. The main reduction has been in the use of perchloroethylene. Other significant reductions have occurred in the area of changing out vapor degreasers which utilized perchloroethylene or methyl chloroform. These degreasers were replaced with ultrasonic cleaners which utilize aqueous detergent for cleaning. Ultrasonic cleaning has many advantages, but the one disadvantage is that it requires a rinse step. Currently, the work on reduction of chlorinate solvents is focused on finding solvents which can be substituted for squirt bottle type applications. Concerns which were addressed when looking at replacement solvents were disposal, compatibility, and health effects.

  17. The Solvent Selection framework: solvents for organic synthesis, separation processes and ionic-organic synthesis

    DEFF Research Database (Denmark)

    Mitrofanov, Igor; Sansonetti, Sascha; Abildskov, Jens;

    2012-01-01

    problems are presented: 1) solvent selection and design for organic synthesis, 2) solvent screening and design of solvent mixtures for pharmaceutical applications and 3) ionic liquids selection and design as solvents. The application of the framework is highlighted successfully through case studies...... focusing on solvent replacement problem in organic synthesis and solvent mixture design for ibuprofen respectively....

  18. Field-usable portable analyzer for chlorinated organic compounds

    Energy Technology Data Exchange (ETDEWEB)

    Buttner, W.J.; Penrose, W.R.; Stetter, J.R. [Transducer Research, Inc., Naperville, IL (United States)

    1995-10-01

    Transducer Research, Inc. (TRI) has been working with the DOE Morgantown Energy Technology Center to develop a new chemical monitor based on a unique sensor which responds selectively to vapors of chlorinated solvents. We are also developing field applications for the monitor in actual DOE cleanup operations. During the initial phase, prototype instruments were built and field tested. Because of the high degree of selectivity that is obtained, no response was observed with common hydrocarbon organic compounds such as BTX (benzene, toluene, xylene) or POLs (petroleum, oil, lubricants), and in fact, no non-halogen-containing chemical has been identified which induces a measurable response. By the end of the Phase I effort, a finished instrument system was developed and test marketed. This instrument, called the RCL MONITOR, was designed to analyze individual samples or monitor an area with automated repetitive analyses. Vapor levels between 0 and 500 ppm can be determined in 90 s with a lower detection limit of 0.2 ppm using the handportable instrument. In addition to the development of the RCL MONITOR, advanced sampler systems are being developed to: (1) extend the dynamic range of the instrument through autodilution of the vapor and (2) allow chemical analyses to be performed on aqueous samples. When interfaced to the samplers, the RCL MONITOR is capable of measuring chlorinated solvent contamination in the vapor phase up to 5000 ppm and in water and other condensed media from 10 to over 10,000 ppb(wt)--without hydrocarbon and other organic interferences.

  19. pH control for enhanced reductive bioremediation of chlorinated solvent source zones

    International Nuclear Information System (INIS)

    Enhanced reductive dehalogenation is an attractive treatment technology for in situ remediation of chlorinated solvent DNAPL source areas. Reductive dehalogenation is an acid-forming process with hydrochloric acid and also organic acids from fermentation of the electron donors typically building up in the source zone during remediation. This can lead to groundwater acidification thereby inhibiting the activity of dehalogenating microorganisms. Where the soils' natural buffering capacity is likely to be exceeded, the addition of an external source of alkalinity is needed to ensure sustained dehalogenation. To assist in the design of bioremediation systems, an abiotic geochemical model was developed to provide insight into the processes influencing the groundwater acidity as dehalogenation proceeds, and to predict the amount of bicarbonate required to maintain the pH at a suitable level for dehalogenating bacteria (i.e., > 6.5). The model accounts for the amount of chlorinated solvent degraded, site water chemistry, electron donor, alternative terminal electron-accepting processes, gas release and soil mineralogy. While calcite and iron oxides were shown to be the key minerals influencing the soil's buffering capacity, for the extensive dehalogenation likely to occur in a DNAPL source zone, significant bicarbonate addition may be necessary even in soils that are naturally well buffered. Results indicated that the bicarbonate requirement strongly depends on the electron donor used and availability of competing electron acceptors (e.g., sulfate, iron (III)). Based on understanding gained from this model, a simplified model was developed for calculating a preliminary design estimate of the bicarbonate addition required to control the pH for user-specified operating conditions.

  20. Biodegradation Kinetics of 1,4-Dioxane in Chlorinated Solvent Mixtures.

    Science.gov (United States)

    Zhang, Shu; Gedalanga, Phillip B; Mahendra, Shaily

    2016-09-01

    This study investigated the impacts of individual chlorinated solvents and their mixtures on aerobic 1,4-dioxane biodegradation by Pseudonocardia dioxanivorans CB1190. The established association of these co-occurring compounds suggests important considerations for their respective biodegradation processes. Our kinetics and mechanistic studies demonstrated that individual solvents inhibited biodegradation of 1,4-dioxane in the following order: 1,1-dichloroethene (1,1-DCE) > cis-1,2-diochloroethene (cDCE) > trichloroethene (TCE) > 1,1,1-trichloroethane (TCA). The presence of 5 mg L(-1) 1,1-DCE completely inhibited 1,4-dioxane biodegradation. Subsequently, we determined that 1,1-DCE was the strongest inhibitor of 1,4-dioxane biodegradation by bacterial pure cultures exposed to chlorinated solvent mixtures as well as in environmental samples collected from a site contaminated with chlorinated solvents and 1,4-dioxane. Inhibition of 1,4-dioxane biodegradation rates by chlorinated solvents was attributed to delayed ATP production and down-regulation of both 1,4-dioxane monooxygenase (dxmB) and aldehyde dehydrogenase (aldH) genes. Moreover, increasing concentrations of 1,1-DCE and cis-1,2-DCE to 50 mg L(-1) respectively increased 5.0-fold and 3.5-fold the expression of the uspA gene encoding a universal stress protein. In situ natural attenuation or enhanced biodegradation of 1,4-dioxane is being considered for contaminated groundwater and industrial wastewater, so these results will have implications for selecting 1,4-dioxane bioremediation strategies at sites where chlorinated solvents are present as co-contaminants. PMID:27486928

  1. Natural and Enhanced Attenuation of Chlorinated Solvents Using RT3D

    Energy Technology Data Exchange (ETDEWEB)

    Johnson, Christian D.; Truex, Michael J.; Clement, T P.

    2006-07-25

    RT3D (Reactive Transport in 3-Dimensions) is a reactive transport code that can be applied to model solute fate and transport for many different purposes. This document specifically addresses application of RT3D for modeling related to evaluation and implementation of Monitored Natural Attenuation (MNA). Selection of MNA as a remedy requires an evaluation process to demonstrate that MNA will meet the remediation goals. The U.S. EPA, through the Office of Solid Waste and Emergency Response (OSWER) Directive 9200.4?17P, provides the regulatory context for the evaluation and implementation of MNA. In a complementary fashion, the context for using fate and transport modeling as part of MNA evaluation is described in the EPA?s technical protocol for chlorinated solvent MNA, the Scenarios Evaluation Tool for Chlorinated Solvent MNA, and in this document. The intent of this document is to describe (1) the context for applying RT3D for chlorinated solvent MNA and (2) the attenuation processes represented in RT3D, (3) dechlorination reactions that may occur, and (4) the general approach for using RT3D reaction modules (including a summary of the RT3D reaction modules that are available) to model fate and transport of chlorinated solvents as part of MNA or for combinations of MNA and selected types of active remediation.

  2. Inferential monitoring of chlorinated solvents through Raman spectroscopic observation of the vibrational modes of water.

    Science.gov (United States)

    Sinfield, Joseph V; Monwuba, Chike

    2016-02-01

    Recent improvements in diode laser, fiber optic, and data acquisition technology have rejuvenated interest in field applications of Raman spectroscopy in a wide range of settings. One such application involves the observation of chlorinated solvents to facilitate the practice of "monitored natural attenuation." In this context, this manuscript focuses on means to improve the sensitivity of in-situ Raman analysis of chlorinated solvents. In particular, the work explores the performance limits of a Time-Resolved Raman Spectroscopy (TRRS) system employed to observe chlorinated solvents in aqueous samples via laboratory tests conducted on both liquid standards of trichloroethylene (TCE) and simulated biodegraded field samples. Quantitative assessment of TCE in solution is carried out through both direct observation of TCE Raman functional groups (381 cm(-1) (δ skeletal), 840 cm(-1) (νCCl) and 1242 cm(-1) (δCH)) and indirect observation of the broad OH stretching (2700-3800 cm(-1)) Raman modes of water. Results from tests on simple solutions show that the TRRS system can detect TCE at aqueous concentrations as low as 70 ppm by directly monitoring the 381 cm(-1) TCE line, whereas observation of the OH stretching line of water (3393 cm(-1)) provides an indirect indication of TCE presence with nearly a 9× improvement in detection level. This unique and counterintuitive mechanism to detect the presence of chlorinated compounds in solution takes advantage of the influence of chlorine on the vibrational modes of water. This influence, which is believed to be attributed to the formation of hydrogen bonds and their resultant interactions with the solvation shell, may serve as a more sensitive and robust indication of the presence of aggregate chlorinated solvent contamination in aqueous systems. Tests performed on simulated biodegraded field samples demonstrate that the indirect detection mechanism is apparent even in complex samples representative of typical field

  3. pH Control for Effective Anaerobic Bioremediation of Chlorinated Solvents

    Science.gov (United States)

    Robinson, C.; Barry, D.; Gerhard, J. I.; Kouznetsova, I.

    2007-12-01

    SABRE (Source Area BioREmediation) is a 4-year collaborative project that aims to evaluate the performance of enhanced anaerobic bioremediation for the treatment of chlorinated solvent DNAPL source areas. The project focuses on a pilot scale demonstration at a trichloroethene (TCE) DNAPL field site, and includes complementary laboratory and modelling studies. Organic acids and hydrogen ions (HCl) typically build up in the treatment zone during anaerobic bioremediation. In aquifer systems with relatively low buffering capacity the generation of these products can cause significant groundwater acidification thereby inhibiting dehalogenating activity. Where the soil buffering capacity is exceeded, addition of buffer may be needed for the effective continuation of TCE degradation. As an aid to the design of remediation schemes, a geochemical model was designed to predict the amount of buffer required to maintain the source zone pH at a suitable level for dechlorinating bacteria (i.e. > 6.5). The model accounts for the amount of TCE to be degraded, site water chemistry, type of organic amendment and soil mineralogy. It assumes complete dechlorination of TCE, and further considers mineral dissolution and precipitation kinetics. The model is applicable to a wide range of sites. For illustration we present results pertinent to the SABRE field site. Model results indicate that, for the extensive dechlorination expected in proximity to the SABRE DNAPL source zone, significant buffer addition may be necessary. Additional simulations are performed to identify buffer requirements over a wider range of field conditions.

  4. Dechlorination progress of chlorinated organic pollutants degraded by use of ionizing radiation in aqueous solutions

    International Nuclear Information System (INIS)

    Kinetics and mechanisms of dechlorination of chlorinated organic pollutants induced by ionizing radiation were described in this article. The progress on the dechlorination of chlorophenols, polychlorinated biphenyl, trichloroethylene, and perchloroethylene involved in radiolysis was also reviewed. In oxidative condition, hydroxyl radical (·OH) would attack chlorophenol to form ·OH-adducts, which could be dechlorinated gradually. However, chlorophenol can be directly reduced by hydrated electron (eaq-) to release Cl-. It was found that radiolytic degradation of polychlorinated biphenyls in organic solvent would release chlorine atoms gradually by chain reactions and the final products were Cl- and biphenyl. Trichloroethylene and tetrachloroethylene mainly reacted with ·OH with the final products of CO2, HCOOH and HCI. As conclusion, the reductive dechlorination of chlorinated organic pollutants possesses advantages of high degradation efficiency, simple products and relatively low radiation dose compared with the oxidation methods. (authors)

  5. POTENTIAL ENHANCEMENTS TO NATURAL ATTENUATION: LINES OF INQUIRY SUPPORTING ENHANCED PASSIVE REMEDIATION OF CHLORINATED SOLVENTS

    Energy Technology Data Exchange (ETDEWEB)

    Vangelas, K; Tom Early, T; Michael Heitkamp, M; Brian02 Looney, B; David Major, D; Brian Riha, B; Jody Waugh, J; Gary Wein, G

    2004-06-18

    The Department of Energy (DOE) is sponsoring an initiative to facilitate efficient, effective and responsible use of Monitored Natural Attenuation (MNA) and Enhanced Passive Remediation (EPR) for chlorinated solvents. This Office of Environmental Management (EM) ''Alternative Project,'' focuses on providing scientific and policy support for MNA/EPR. A broadly representative working group of scientists supports the project along with partnerships with regulatory organizations such as the Interstate Technology and Regulatory Council and the U.S. Environmental Protection Agency (EPA). The initial product of the technical working group was a summary report that articulated the conceptual approach and central scientific tenants of the project, and that identified a prioritized listing of technical targets for field research. This report documented the process in which: (1) scientific ground rules were developed, (2) lines of inquiry were identified and then critically evaluated, (3) promising applied research topics were highlighted in the various lines of inquiry, and (4) these were discussed and prioritized. The summary report will serve as a resource to guide management and decision-making throughout the period of the subject MNA/EPR Alternative Project. To support and more fully document the information presented in the summary report, we are publishing a series of supplemental documents that present the full texts from the technical analyses within the various lines of inquiry (see listing). The following report - documenting our evaluation of the state of the science of the characterization and monitoring process and tools-- is one of those supplemental documents.

  6. Handbook of organic solvent properties

    CERN Document Server

    Smallwood, Ian

    2012-01-01

    The properties of 72 of the most commonly used solvents are given, tabulated in the most convenient way, making this book a joy for industrial chemists to use as a desk reference. The properties covered are those which answer the basic questions of: Will it do the job? Will it harm the user? Will it pollute the air? Is it easy to handle? Will it pollute the water? Can it be recovered or incinerated? These are all factors that need to be considered at the early stages of choosing a solvent for a new product or process.A collection of the physical properties of most commonly used solvents, their

  7. Method of stripping metals from organic solvents

    Science.gov (United States)

    Todd, Terry A.; Law, Jack D.; Herbst, R. Scott; Romanovskiy, Valeriy N.; Smirnov, Igor V.; Babain, Vasily A.; Esimantovski, Vyatcheslav M.

    2009-02-24

    A new method to strip metals from organic solvents in a manner that allows for the recycle of the stripping agent. The method utilizes carbonate solutions of organic amines with complexants, in low concentrations, to strip metals from organic solvents. The method allows for the distillation and reuse of organic amines. The concentrated metal/complexant fraction from distillation is more amenable to immobilization than solutions resulting from current practice.

  8. A fully operational pilot plant for eliminating radioactive oils mixed with chlorinated solvents - 59044

    International Nuclear Information System (INIS)

    Disposal of organic liquid waste has become an increasing issue for many nuclear sites. Existing disposal solutions such as incineration or super critical water techniques are not compatible with wastes containing chlorinated solvents or fluorine owing to corrosion problems. As an example several hundred cubic meters of lubricating oils mixed with trichloroethylene (TCE) or perchloroethylene (PCE) are stockpiled on several French nuclear sites. For several years Dewdrops has been developing an original combination of mineralization processes for waste oils and solvents particularly well suited to the nuclear field. The patented technology relies on the alternation of chemical and biological oxidation mechanisms. The oxidized organic material predominately forms carbon dioxide, water and inorganic salts. This paper details the procedure and the results obtained for a particular case at the Tricastin nuclear site of Areva NC (South France). The organic waste used in this study was a 85/15 v/v ratio mix of lubricating oil and TCE. The pilot plant build upon the technology has a daily treatment capacity of approximately 10 liters. In the first step the TCE is mineralized by the photo Fenton reaction. Using hydrogen peroxide with an ultraviolet regenerated iron catalyst, TCE is transformed to carbon dioxide, water and hydrochloric acid. After neutralizing with caustic soda, the next step is a multi-stage biodegradation process to eliminate the remaining lubricating oil. Carefully selected microorganisms use the organic waste as an energy source for their metabolism. During oil biodegradation over 75% of the carbon is released as carbon dioxide while the remaining is incorporated into the biomass. The aqueous phase is continuously separated from the biomass using cross flow filters. The output aqueous phase is treated with ozone and ultraviolet light to eliminate the remaining organic compounds. The final effluent obtained is in conformance with European water standards

  9. Organic Solvent Tolerant Lipases and Applications

    Directory of Open Access Journals (Sweden)

    Shivika Sharma

    2014-01-01

    Full Text Available Lipases are a group of enzymes naturally endowed with the property of performing reactions in aqueous as well as organic solvents. The esterification reactions using lipase(s could be performed in water-restricted organic media as organic solvent(s not only improve(s the solubility of substrate and reactant in reaction mixture but also permit(s the reaction in the reverse direction, and often it is easy to recover the product in organic phase in two-phase equilibrium systems. The use of organic solvent tolerant lipase in organic media has exhibited many advantages: increased activity and stability, regiospecificity and stereoselectivity, higher solubility of substrate, ease of products recovery, and ability to shift the reaction equilibrium toward synthetic direction. Therefore the search for organic solvent tolerant enzymes has been an extensive area of research. A variety of fatty acid esters are now being produced commercially using immobilized lipase in nonaqueous solvents. This review describes the organic tolerance and industrial application of lipases. The main emphasis is to study the nature of organic solvent tolerant lipases. Also, the potential industrial applications that make lipases the biocatalysts of choice for the present and future have been presented.

  10. Organic solvent regeneration of granular activated carbon

    Science.gov (United States)

    Cross, W. H.; Suidan, M. T.; Roller, M. A.; Kim, B. R.; Gould, J. P.

    1982-09-01

    The use of activated carbon for the treatment of industrial waste-streams was shown to be an effective treatment. The high costs associated with the replacement or thermal regeneration of the carbon have prohibited the economic feasibility of this process. The in situ solvent regeneration of activated carbon by means of organic solvent extraction was suggested as an economically alternative to thermal regeneration. The important aspects of the solvent regeneration process include: the physical and chemical characteristics of the adsorbent, the pore size distribution and energy of adsorption associated with the activated carbon; the degree of solubility of the adsorbate in the organic solvent; the miscibility of the organic solvent in water; and the temperature at which the generation is performed.

  11. Microbial diversity in a hydrocarbon- and chlorinated-solvent- contaminated aquifer undergoing intrinsic bioremediation

    Science.gov (United States)

    Dojka, M.A.; Hugenholtz, P.; Haack, S.K.; Pace, N.R.

    1998-01-01

    A culture-independent molecular phylogenetic approach was used to survey constituents of microbial communities associated with an aquifer contaminated with hydrocarbons (mainly jet fuel) and chlorinated solvents undergoing intrinsic bioremediation. Samples were obtained from three redox zones: methanogenic, methanogenic-sulfate reducing, and iron or sulfate reducing. Small-subunit rRNA genes were amplified directly from aquifer material DNA by PCR with universally conserved or Bacteria- or Archaea-specific primers and were cloned. A total of 812 clones were screened by restriction fragment length polymorphisms (RFLP), approximately 50% of which were unique. All RFLP types that occurred more than once in the libraries, as well as many of the unique types, were sequenced. A total of 104 (94 bacterial and 10 archaeal) sequence types were determined. Of the 94 bacterial sequence types, 10 have no phylogenetic association with known taxonomic divisions and are phylogenetically grouped in six novel division level groups (candidate divisions WS1 to WS6); 21 belong to four recently described candidate divisions with no cultivated representatives (OPS, OP8, OP10, and OP11); and 63 are phylogenetically associated with 10 well-recognized divisions. The physiology of two particularly abundant sequence types obtained from the methanogenic zone could be inferred from their phylogenetic association with groups of microorganisms with a consistent phenotype. One of these sequence types is associated with the genus Syntrophus; Syntrophus spp. produce energy from the anaerobic oxidation of organic acids, with the production of acetate and hydrogen. The organism represented by the other sequence type is closely related to Methanosaeta spp., which are known to be capable of energy generation only through aceticlastic methanogenesis. We hypothesize, therefore, that the terminal step of hydrocarbon degradation in the methanogenic zone of the aquifer is aceticlastic methanogenesis and

  12. Performance of an anaerobic, static bed, fixed film bioreactor for chlorinated solvent treatment

    Science.gov (United States)

    Lorah, Michelle M.; Walker, Charles; Graves, Duane

    2015-01-01

    Anaerobic, fixed film, bioreactors bioaugmented with a dechlorinating microbial consortium were evaluated as a potential technology for cost effective, sustainable, and reliable treatment of mixed chlorinated ethanes and ethenes in groundwater from a large groundwater recovery system. Bench- and pilot-scale testing at about 3 and 13,500 L, respectively, demonstrated that total chlorinated solvent removal to less than the permitted discharge limit of 100 μg/L. Various planned and unexpected upsets, interruptions, and changes demonstrated the robustness and reliability of the bioreactor system, which handled the operational variations with no observable change in performance. Key operating parameters included an adequately long hydraulic retention time for the surface area, a constant supply of electron donor, pH control with a buffer to minimize pH variance, an oxidation reduction potential of approximately −200 millivolts or lower, and a well-adapted biomass capable of degrading the full suite of chlorinated solvents in the groundwater. Results indicated that the current discharge criteria can be met using a bioreactor technology that is less complex and has less downtime than the sorption based technology currently being used to treat the groundwater.

  13. Chlorinated organic compounds produced by Fusarium graminearum.

    Science.gov (United States)

    Ntushelo, Khayalethu

    2016-06-01

    Fusarium graminearum, a pathogen of wheat and maize, not only reduces grain yield and degrades quality but also produces mycotoxins in the infected grain. Focus has been on mycotoxins because of the human and animal health hazards associated with them. In addition to work done on mycotoxins, chemical profiling of F. graminearum to identify other compounds produced by this fungus remains critical. With chemical profiling of F. graminearum the entire chemistry of this fungus can be understood. The focus of this work was to identify chlorinated compounds produced by F. graminearum. Various chlorinated compounds were detected and their role in F. graminearum is yet to be understood. PMID:27165533

  14. Remediation of Chlorinated Solvent Plumes Using In-Situ Air Sparging—A 2-D Laboratory Study

    Directory of Open Access Journals (Sweden)

    Jeffrey A. Adams

    2011-06-01

    Full Text Available In-situ air sparging has evolved as an innovative technique for soil and groundwater remediation impacted with volatile organic compounds (VOCs, including chlorinated solvents. These may exist as non-aqueous phase liquid (NAPL or dissolved in groundwater. This study assessed: (1 how air injection rate affects the mass removal of dissolved phase contamination, (2 the effect of induced groundwater flow on mass removal and air distribution during air injection, and (3 the effect of initial contaminant concentration on mass removal. Dissolved-phase chlorinated solvents can be effectively removed through the use of air sparging; however, rapid initial rates of contaminant removal are followed by a protracted period of lower removal rates, or a tailing effect. As the air flow rate increases, the rate of contaminant removal also increases, especially during the initial stages of air injection. Increased air injection rates will increase the density of air channel formation, resulting in a larger interfacial mass transfer area through which the dissolved contaminant can partition into the vapor phase. In cases of groundwater flow, increased rates of air injection lessened observed downward contaminant migration effect. The air channel network and increased air saturation reduced relative hydraulic conductivity, resulting in reduced groundwater flow and subsequent downgradient contaminant migration. Finally, when a higher initial TCE concentration was present, a slightly higher mass removal rate was observed due to higher volatilization-induced concentration gradients and subsequent diffusive flux. Once concentrations are reduced, a similar tailing effect occurs.

  15. Electrokinetic-enhanced bioaugmentation for remediation of chlorinated solvents contaminated clay.

    Science.gov (United States)

    Mao, Xuhui; Wang, James; Ciblak, Ali; Cox, Evan E; Riis, Charlotte; Terkelsen, Mads; Gent, David B; Alshawabkeh, Akram N

    2012-04-30

    Successful bioremediation of contaminated soils is controlled by the ability to deliver bioremediation additives, such as bacteria and/or nutrients, to the contaminated zone. Because hydraulic advection is not practical for delivery in clays, electrokinetic (EK) injection is an alternative for efficient and uniform delivery of bioremediation additive into low-permeability soil and heterogeneous deposits. EK-enhanced bioaugmentation for remediation of clays contaminated with chlorinated solvents is evaluated. Dehalococcoides (Dhc) bacterial strain and lactate ions are uniformly injected in contaminated clay and complete dechlorination of chlorinated ethene is observed in laboratory experiments. The injected bacteria can survive, grow, and promote effective dechlorination under EK conditions and after EK application. The distribution of Dhc within the clay suggests that electrokinetic transport of Dhc is primarily driven by electroosmosis. In addition to biodegradation due to bioaugmentation of Dhc, an EK-driven transport of chlorinated ethenes is observed in the clay, which accelerates cleanup of chlorinated ethenes from the anode side. Compared with conventional advection-based delivery, EK injection is significantly more effective for establishing microbial reductive dechlorination capacity in low-permeability soils. PMID:22365139

  16. ADVANCING THE SCIENCE OF NATURAL AND ENHANCED ATTENUATION FOR CHLORINATED SOLVENTS

    Energy Technology Data Exchange (ETDEWEB)

    Looney, B; TOM O. EARLY, T; TYLER GILMORE, T; FRANCIS H. CHAPELLE, F; NORMAN H. CUTSHALL, N; JEFF ROSS, J; MARK ANKENY, M; Michael Heitkamp, M; DAVID MAJOR, D; CHARLES J. NEWELL, C; W. JODY WAUGH, W; GARY WEIN, G; Karen Vangelas, K; Karen-M Adams, K; CLAIRE H. SINK, C

    2006-12-27

    This report summarizes the results of a three-year program that addressed key scientific and technical aspects related to natural and enhanced attenuation of chlorinated organics. The results from this coordinated three-year program support a variety of technical and regulatory advancements. Scientists, regulators, engineers, end-users and stakeholders participated in the program, which was supported by the U.S. Department of Energy (DOE) and the Interstate Technology and Regulatory Council (ITRC). The overarching objective of the effort was to examine environmental remedies that are based on natural processes--remedies such as Monitored Natural Attenuation (MNA) or Enhanced Attenuation (EA). A key result of the recent effort was the general affirmation of the approaches and guidance in the original U.S. Environmental Protection Agency (EPA) chlorinated solvent MNA protocols and directives from 1998 and 1999, respectively. The research program did identify several specific opportunities for advances based on: (1) mass balance as the central framework for attenuation based remedies, (2) scientific advancements and achievements during the past ten years, (3) regulatory and policy development and real-world experience using MNA, and (4) exploration of various ideas for integrating attenuation remedies into a systematic set of ''combined remedies'' for contaminated sites. These opportunities are summarized herein and are addressed in more detail in referenced project documents and journal articles, as well as in the technical and regulatory documents being developed within the ITRC. Natural attenuation processes occur in all soil and groundwater systems and act, to varying degrees, on all contaminants. Thus, a decision to rely on natural attenuation processes as part of a site-remediation strategy does not depend on the occurrence of natural attenuation, but on its effectiveness in meeting site-specific remediation goals. Meeting these goals

  17. Peroxone activated persulfate treatment of 1,4-dioxane in the presence of chlorinated solvent co-contaminants.

    Science.gov (United States)

    Eberle, Dylan; Ball, Raymond; Boving, Thomas B

    2016-02-01

    1,4-dioxane is often found as a co-contaminant with chlorinated volatile organic compounds (VOCs) at solvent release sites such as landfills, solvent recycling facilities, or fire training areas. Historically, soil and groundwater samples were not routinely analyzed for 1,4-dioxane and therefore the number of known 1,4-dioxane sites is still increasing. Due to its co-occurrence with chlorinated compounds, remediation strategies are needed that simultaneously treat both 1,4-dioxane as well as chlorinated VOC co-contaminants. In this proof of concept laboratory study, the fate of 1,4-dioxane was examined during the targeted destruction of aqueous phase VOC, using a peroxone activated persulfate (PAP) chemical oxidation method. Bench-scale experiments were carried out to evaluate the treatability of 1,4-dioxane as both a single-contaminant and in the presence of trichloroethene (TCE), and 1,1,1-trichloroethane (1,1,1-TCA). Possible dependencies on oxidant concentration and reaction kinetics were studied. The oxidative destruction of 1,4-dioxane, TCE and 1,1,1-TCA in single-contaminant batch systems followed pseudo-first-order reaction kinetics and even at the most dilute oxidant concentration lasted for at least 13 days. The rate of oxidation for each contaminant increased linearly with increasing persulfate concentration over the range of oxidant concentrations tested. The rate of oxidative destruction, from most easily degraded to least, was: TCE > 1,4-dioxane > 1,1,1-TCA. Oxidation rates were up to 87% slower in a mixture of these three compounds. Although additional tests are necessary, our data suggest that PAP oxidation of 1,4-dioxane might aid in the cleanup of VOC contaminated sites. PMID:26408980

  18. Chlorinated organic pesticides in marketed food: Barcelona, 2001-06

    International Nuclear Information System (INIS)

    This paper reports concentration levels of 22 chlorinated organic compounds (both primary compounds and metabolites) in food marketed in the city of Barcelona (Catalonia, Spain) in 2001-06. Samples included meat products, fish and seafood, eggs, milk and dairy, vegetal oils, cereal products and derivates, vegetables, fresh fruits, dry fruits, spices, formula and baby food, tea and wine. Levels of chlorinated organic compounds were determined by gas chromatography with selective detectors: electron capture (ECD), flame photometric (FPD) and confirmation with mass-spectrometry. Chlorinated organic pesticides were detected in 7 of the 1,484 samples analyzed in the 2001-06 period (0.5%): 1 dairy product, 1 fruit, 1 olive oil and 4 vegetables. Specific pesticides detected are lindane and endosulfan α, β or sulphate. A decrease in both the proportion of samples with detectable residues and in the variety of chlorinated pesticides found is visible when comparing these results with those of the previous 1989-2000 period. These results suggest the gradual disappearance of regulated chlorinated organic pesticides as a consequence of the growing worldwide implementation of current regulatory agreements

  19. Electrokinetic-enhanced bioaugmentation for remediation of chlorinated solvents contaminated clay

    Energy Technology Data Exchange (ETDEWEB)

    Mao, Xuhui, E-mail: x.mao@neu.edu [Civil and Environmental Engineering Department, Northeastern University, Boston, MA 02115 (United States); School of Resources and Environmental Science, Wuhan University, Wuhan 430079 (China); Wang, James [Geosyntec Consultants, Columbia, MA (United States); Ciblak, Ali [Civil and Environmental Engineering Department, Northeastern University, Boston, MA 02115 (United States); Cox, Evan E. [Geosyntec Consultants, Columbia, MA (United States); Riis, Charlotte [NIRAS A/S, Alleroed (Denmark); Terkelsen, Mads [Capital Region of Denmark, Hilleroed (Denmark); Gent, David B. [Environmental Laboratory, Engineer Research and Development Center (ERDC), US Army Corps of Engineers, Vicksburg, MS (United States); Alshawabkeh, Akram N., E-mail: aalsha@neu.edu [Civil and Environmental Engineering Department, Northeastern University, Boston, MA 02115 (United States)

    2012-04-30

    Highlights: Black-Right-Pointing-Pointer Simultaneous delivery of electron donors and bacteria into low permeability clays. Black-Right-Pointing-Pointer Bacteria injection, growth and consequent transformation of contaminants are viable. Black-Right-Pointing-Pointer EK injection is more effective than advection-based injection for clay soil. Black-Right-Pointing-Pointer Electroosmosis appears to be the driving mechanism for bacteria injection. Black-Right-Pointing-Pointer Both EK transport and biodegradation contribute the removal of VOCs in clay. - Abstract: Successful bioremediation of contaminated soils is controlled by the ability to deliver bioremediation additives, such as bacteria and/or nutrients, to the contaminated zone. Because hydraulic advection is not practical for delivery in clays, electrokinetic (EK) injection is an alternative for efficient and uniform delivery of bioremediation additive into low-permeability soil and heterogeneous deposits. EK-enhanced bioaugmentation for remediation of clays contaminated with chlorinated solvents is evaluated. Dehalococcoides (Dhc) bacterial strain and lactate ions are uniformly injected in contaminated clay and complete dechlorination of chlorinated ethene is observed in laboratory experiments. The injected bacteria can survive, grow, and promote effective dechlorination under EK conditions and after EK application. The distribution of Dhc within the clay suggests that electrokinetic transport of Dhc is primarily driven by electroosmosis. In addition to biodegradation due to bioaugmentation of Dhc, an EK-driven transport of chlorinated ethenes is observed in the clay, which accelerates cleanup of chlorinated ethenes from the anode side. Compared with conventional advection-based delivery, EK injection is significantly more effective for establishing microbial reductive dechlorination capacity in low-permeability soils.

  20. In situ thermally enhanced biodegradation of petroleum fuel hydrocarbons and halogenated organic solvents

    International Nuclear Information System (INIS)

    An in situ thermally enhanced microbial remediation strategy and a method for the biodegradation of toxic petroleum fuel hydrocarbon and halogenated organic solvent contaminants are described. The method utilizes nonpathogenic, thermophilic bacteria for the thermal biodegradation of toxic and carcinogenic contaminants, such as benzene, toluene, ethylbenzene and xylenes, from fuel leaks and the chlorinated ethenes, such as trichloroethylene, chlorinated ethanes, such as 1,1,1-trichloroethane, and chlorinated methanes, such as chloroform, from past solvent cleaning practices. The method relies on and takes advantage of the pre-existing heated conditions and the array of delivery/recovery wells that are created and in place following primary subsurface contaminant volatilization efforts via thermal approaches, such as dynamic underground steam-electrical heating. 21 figs

  1. A marine sink for chlorine in natural organic matter

    Science.gov (United States)

    Leri, Alessandra C.; Mayer, Lawrence M.; Thornton, Kathleen R.; Northrup, Paul A.; Dunigan, Marisa R.; Ness, Katherine J.; Gellis, Austin B.

    2015-08-01

    Chloride--the most abundant ion in sea water--affects ocean salinity, and thereby seawater density and ocean circulation. Its lack of reactivity gives it an extremely long residence time. Other halogens are known to be incorporated into marine organic matter. However, evidence of similar transformations of seawater chloride is lacking, aside from emissions of volatile organochlorine by marine algae. Here we report high organochlorine concentrations from 180 to 700 mg kg-1 in natural particulate organic matter that settled into sediment traps at depths between 800 and 3,200 m in the Arabian Sea, taken between 1994 and 1995. X-ray spectromicroscopic imaging of chlorine bonding reveals that this organochlorine exists primarily in concentrated aliphatic forms consistent with lipid chlorination, along with a more diffuse aromatic fraction. High aliphatic organochlorine in particulate material from cultured phytoplankton suggests that primary production is a source of chlorinated organic matter. We also found that particulate algal detritus can act as an organic substrate for abiotic reactions involving Fe2+, H2O2 or light that incorporate chlorine into organic matter at levels up to several grams per kilogram. We conclude that transformations of marine chloride to non-volatile organochlorine through biological and abiotic pathways represent an oceanic sink for this relatively unreactive element.

  2. Hydrodynamic and isotopic characterization of a site contaminated by chlorinated solvents: Chienti River Valley, Central Italy

    International Nuclear Information System (INIS)

    Highlights: ► The fate of chlorinated solvents in groundwater in an alluvial aquifer has been investigated. ► Heterogeneity of the aquifer sediments causes vertical components of groundwater flow. ► Multilevel data shows the VOC’s stratification in the aquifer. ► Concentration and δ13C and δ37Cl data showed that dilution controls the VOC’s distribution. ► Biodegradation has been confirmed by isotope data only in low permeability layers. - Abstract: Contaminant sources have been attributed to shoe manufacturers in an alluvial aquifer located along 26 km2 in the Chienti River Valley, Central Italy. During the 1980s and 1990s, the main chlorinated compound used in the study area was 1,1,1-Trichloroethane (1,1,1-TCA), which was substituted by Perchloroethene (PCE) in the last 15 years. A hydrogeological conceptual model has been developed for the alluvial aquifer taking into account the presence of low permeability lenses, forming a multilayer semi-confined aquifer. Hydrodynamic tests (pumping and flowmeter heat-pulse tests) coupled with standard and multilevel hydrochemical and isotopic samplings were performed. Flowmeter tests showed the existence of vertical flow between aquifer levels having different permeability. Physical–chemical parameter logs agreed with the existence of a multilayer aquifer. Concentration data collected in 21 wells located downgradient of the different sources revealed VOC (Volatile Organic Compound) levels lower than 100 μg/L in the upper part of the valley and levels reaching about 200 μg/L in the near shore areas. PCE is the main compound present in the aquifer. No evidence of the presence of TCA was found in the upper areas of the Chienti Valley, but in the areas near the shore, TCA and its degradation products are predominant. Data collected at multilevels located at two sites (upper and near shore areas) to refine the results obtained in the regional survey show a stratification of the VOC concentrations; values of

  3. Occurrence of Sustained Treatment Following Enhanced Anaerobic Bioremediation at Chlorinated Solvent Sites

    Science.gov (United States)

    Burcham, M.; Bedient, P.; McGuire, T.; Adamson, D.; Newell, C. J.

    2012-12-01

    Chlorinated solvents are among the most prevalent groundwater contaminants found in the United States, located at nearly 80% of all Superfund sites, and at more than 3,000 Department of Defense sites. Responsible parties in the U.S. spend several billion dollars per year on environmental restoration with much of these funds targeting remediation of chlorinated solvents in groundwater. To make this large investment in groundwater remediation technologies more effective, end-users need quantitative, accurate, and reliable performance data for commonly used remediation technologies. One such technology that has been used increasingly for remediation of chlorinated solvent sites is enhanced anaerobic bioremediation (EAB). A previous study of remediation performance of various technologies indicated that EAB has the potential for sustained treatment several years after injection of an EAB substrate. This benefit is attributed to the recycling of decaying biomass (endogenous decay) and/or the formation of reactive mineral species, and it serves to mitigate the incidence of concentration rebound during the post-treatment period that is commonly-observed with other technologies. The current study expands on the previous study by focusing on the occurrence of sustained treatment at EAB sites through analysis of groundwater concentration data for longer post-treatment periods than were available for the previous study (up to 9 years), along with site characteristics such as hydrogeology, geochemistry, and microbiology. The objective is to determine whether relationships exist that can aid in determining when sustained treatment following EAB might occur for a given site. To date, data from over 17 distinct sites applying EAB have been collected. The dataset includes over 50 monitoring wells within EAB treatment zones, with concentration data extending from before treatment began to more than 3 to 9 years following treatment. Efforts are underway to continue this data mining

  4. Organic solvent nanofiltration: prospects and application

    International Nuclear Information System (INIS)

    The key lines of research in a new field of the membrane science and technology, viz., organic solvent nanofiltration, are considered. The prospects for its use in chemical, petrochemical and food industries are discussed. Attention is focused on membranes developed for this method.

  5. Organic solvent nanofiltration: prospects and application

    Energy Technology Data Exchange (ETDEWEB)

    Volkov, A V; Korneeva, G A; Tereshchenko, Gennadii F [A. V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Moscow (Russian Federation)

    2008-11-30

    The key lines of research in a new field of the membrane science and technology, viz., organic solvent nanofiltration, are considered. The prospects for its use in chemical, petrochemical and food industries are discussed. Attention is focused on membranes developed for this method.

  6. Activated Persulfate Treatment of 1,4-Dioxane in the Presence of Chlorinated Solvent Co-contaminants

    Science.gov (United States)

    Boving, T. T.; Eberle, D. E. H.; Ball, R.

    2014-12-01

    1,4-dioxane is an emerging groundwater contaminant and a likely human carcinogen. Due to its history as a stabilizer in chlorinated solvents, 1,4-dioxane is often found as a co-contaminant at solvent releases sites such as landfills, solvent recycling facilities, vapor decreasing operations, and fire-training areas. Historically, 1,4-dioxane was not routinely analyzed for at solvent release sites. The lack of analyses and the limitations of the analyses that were performed (i.e. high reporting limits) means that the scale of 1,4-dioxane subsurface contamination is still emerging. With the number of known 1,4-dioxane sites increasing, the need for cost effective 1,4-dioxane remediation technologies is rising as well. Remediation strategies that are capable of treating both 1,4-dioxane as well as chlorinated co-contaminants are of particular importance, especially when treating mixed-waste source zones. In the present study, we examined the fate of 1,4-dioxane during the targeted remediation of aqueous phase volatile organic compounds (VOC) using an activated persulfate based ISCO method (OxyZone®). Bench scale laboratory experiments are used to evaluate the treatability of 1,4-dioxane both as a single compound and in the presence of trichloroethene (TCE) and 1,1,1-trichloroethane (1,1,1-TCA). Possible dependencies on oxidant concentration and reaction kinetics were studied. Preliminary results are promising and show that OxyZone® is persistent and long lived, with oxidation of 1,4-dioxane continuing more than 12 days after initial dosage, even at dilute oxidant concentrations. The oxidative destruction of 1,4-dioxane, TCE and 1,1,1-TCA in single compound batch systems followed pseudo first order reaction kinetics. The rate of oxidation for each contaminant increased linearly with increasing persulfate concentration over the range of oxidant concentrations tested. The rate of oxidative destruction, from most easily degraded to least was: TCE > 1,4-Dioxane > 1

  7. Variation in assimilable organic carbon formation during chlorination of Microcystis aeruginosa extracellular organic matter solutions.

    Science.gov (United States)

    Sun, Xingbin; Yuan, Ting; Ni, Huishan; Li, Yanpeng; Hu, Yang

    2016-07-01

    This study investigated the chlorination of Microcystis aeruginosa extracellular organic matter (EOM) solutions under different conditions, to determine how the metabolites produced by these organisms affect water safety and the formation of assimilable organic carbon (AOC). The effects of chlorine dosages, coagulant dosage, reaction time and temperature on the formation of AOC were investigated during the disinfection of M.aeruginosa metabolite solutions. The concentration of AOC followed a decreasing and then increasing pattern with increasing temperature and reaction time. The concentration of AOC decreased and then increased with increasing chlorination dosage, followed by a slight decrease at the highest level of chlorination. However, the concentration of AOC decreased continuously with increasing coagulant dosage. The formation of AOC can be suppressed under appropriate conditions. In this study, chlorination at 4mg/L, combined with a coagulant dose of 40mg/L at 20°C over a reaction time of 12hr, produced the minimum AOC. PMID:27372113

  8. Chlorinated and nitrogenous disinfection by-product formation from ozonation and post-chlorination of natural organic matter surrogates.

    Science.gov (United States)

    Bond, Tom; Templeton, Michael R; Rifai, Omar; Ali, Hussain; Graham, Nigel J D

    2014-09-01

    Ozonation before chlorination is associated with enhanced formation of chloropicrin, a halonitromethane disinfection by-product (DBP), during drinking water treatment. In order to elucidate reasons for this, five natural organic matter (NOM) surrogates were treated using both chlorination and ozonation-chlorination under controlled laboratory conditions. Selected surrogates comprised two phenolic compounds, two free amino acids and one dipeptide; these were resorcinol, 3-aminophenol, L-aspartic acid, β-alanine and ala-ala, respectively. Quantified DBPs included chloropicrin, chloroform, dichloroacetonitrile and trichloroacetonitrile. Relative to chlorination alone, increases in the formation of chloropicrin from ozonation-chlorination varied from 138% for 3-aminophenol to 3740% for ala-ala for the four amine surrogates. This indicates that ozone is more effective than chlorine in mediating a rate-limiting oxidation step in chloropicrin formation, most plausibly involving conversion of an amine group to a nitro group. While both hydrophilic and hydrophobic surrogates acted as chloropicrin precursors, ala-ala was the most reactive precursor following ozonation-chlorination. Since peptides are far commoner in drinking water sources than free amino acids, further research into chemical oxidation of these species by ozone and chlorine is recommended. In contrast, oxidation with ozone prior to chlorination reduced chloroform formation moderately for the two phenolic compounds.

  9. Indentation of polydimethylsiloxane submerged in organic solvents

    OpenAIRE

    Hu, Yuhang; Chen, Xin; Whitesides, George McClelland; Vlassak, Joost J.; Suo, Zhigang

    2011-01-01

    This work uses a method based on indentation to characterize a polydimethylsiloxane (PDMS) elastomer submerged in an organic solvent (decane, heptane, pentane, or cyclohexane). An indenter is pressed into a disk of a swollen elastomer to a fixed depth, and the force on the indenter is recorded as a function of time. By examining how the relaxation time scales with the radius of contact, one can differentiate the poroelastic behavior from the viscoelastic behavior. By matching the relaxation c...

  10. Organic Solvent Tropical Report [SEC 1 and 2

    Energy Technology Data Exchange (ETDEWEB)

    COWLEY, W.L.

    2000-06-21

    This report provides the basis for closing the organic solvent safety issue. Sufficient information is presented to conclude that risk posed by an unmitigated organic solvent fire is within risk evaluation guidelines.

  11. Chlorine

    Energy Technology Data Exchange (ETDEWEB)

    Talmage, Sylvia Smith [ORNL

    2009-01-01

    Following a brief description of the use of chlorine as a chemical warfare agent in World War I, this chapter summarizes physical and chemical data and recent clinical and controlled laboratory studies on the irritant and lethal effects of chlorine. The mechanism of toxicity for both irritation and lethal effects is described. The mathematical relationship between concentration and exposure duration for a set endpoint is given for both an irritancy response and mortality. This information can be used to assist in time-scaling for the set endpoint to other exposure durations. Risk assessment addresses the potential for greater effects in sensitive populations such as asthmatics. A concentration of 0.5 ppm for up to 8 hours is a no-adverse-effect concentration in most sensitive subjects; whereas, a concentration of 1.0 ppm induces some sensory irritation and transient changes in respiratory tract airflow parameters. Treatment and intervention of exposed individuals is dependent upon symptoms

  12. Application of microbial biomass and activity measures to assess in situ bioremediation of chlorinated solvents

    International Nuclear Information System (INIS)

    Evaluating the effectiveness of chlorinated solvent remediation in the subsurface can be a significant problem given uncertainties in estimating the total mass of contaminants present. If the remediation technique is a biological activity, information on the progress and success of the remediation may be gained by monitoring changes in the mass and activities of microbial populations. The in situ bioremediation demonstration at the US Department of Energy (DOE) Savannah River Site (SRS) is designed to test the effectiveness of methane injection for the stimulation of in sediments. Past studies have shown the potential for degradation by native microbial populations. The design and implementation of the SRS Integrated Demonstration is described in this volume. A control phase without treatment was followed by a phase withdrawing air. The next phase included vacuum extraction plus air injection into the lower horizontal well located below the water table. The next period included the injection of 1% methane in air followed by injection of 4% methane in air. Based on the literature, it was hypothesized that the injection of methane would stimulate methanotrophic populations and thus accelerate biological degradation of TCE. Measuring the success of bioremediation is a complex effort that includes monitoring of changes in microbial populations associated with TCE degradation. These monitoring efforts are described in this paper and in related papers in this volume

  13. Field-usable portable analyzer for chlorinated organic compounds. Topical report, September 1992--May 1994

    Energy Technology Data Exchange (ETDEWEB)

    Buttner, W.J.; Williams, R.D.

    1995-05-01

    Through a U.S. DOE-funded program, an advanced chlorinated organic (RCL) vapor monitor has been built and tested in actual hazardous waste site operations. The monitor exploits the analytical capabilities of a solid-state sensor which was recently developed and has remarkable selectivity for chlorinated organic vapors at sub-parts-per-million sensitivity. The basic design goal of a user-friendly, reliable, instrument with a broad dynamic range for the selective detection of chlorinated solvent vapors was demonstrated. To date, no non-halogen-containing compound has been identified that induces a measurable response on the sensor, including commonly encountered contaminants such as BTXs (benzene, toluene, and xylenes) or POLs (petroleum, oils, lubricants). In addition to the development of the RCL MONITOR, advanced sampler systems were developed to further extend the analytical capability of this instrument, allowing chemical analyses to be performed for both vapor phase and condensed contamination. The sampling methods include fixed dilution, preconcentration, and closed-loop air stripping for condensed media. With uniform success, these different series of field tests were conducted at DOE facilities on several types of samples. Independent cost-benefit analysis has concluded that significant cost savings can be achieved using the RCL MONITOR in DOE applications. This effort provides a sound fundamental technology base for the development of advanced analytical methods that are needed by the US DOE. In addition, advanced methods for detecting chlorinated hydrocarbons that are made possible by this technology will save time, reduce costs, and improve human health and safety in restoration operations. To fully achieve all possible cost savings, continued effort is necessary to develop validated methods for the use of the RCL MONITOR. The development of methods through case studies is the theme of the Phase II effort, which is currently underway.

  14. Identification of Chlorinated Solvent Sources in the Indoor Air of Private Residences around Hill Air Force Base, Utah

    OpenAIRE

    Hall, Andrew Jensen

    2008-01-01

    Volatile chlorinated solvents such as trichloroethylene (TCE), 1,2 dichloroethane (1,2 DCA), and perchloroethylene (PCE) have been identified in the indoor air of residences located near Hill Air Force Base (AFB), Utah. These vapors can originate from either volatilization of contaminates from shallow contaminated groundwater and transport into residences or from sources within the residence. The focus of the thesis was the development of a testing strategy for determining sources of TCE, 1,2...

  15. A study of chlorinated solvent contamination of the aquifers of an industrial area in central Italy: a possibility of bioremediation

    OpenAIRE

    Matteucci, Federica; Ercole, Claudia; del Gallo, Maddalena

    2015-01-01

    Perchloroethene, trichloroethene, and other chlorinated solvents are widespread groundwater pollutants. They form dense non-aqueous phase liquids that sink through permeable groundwater aquifers until non-permeable zone is reached. In Italy, there are many situations of serious contamination of groundwater that might compromise their use in industry, agriculture, private, as the critical case of a Central Italy valley located in the province of Teramo (“Val Vibrata”), characterized by a signi...

  16. Summary of findings on evaluation of aqueous degreasers versus chlorinated solvents at the Paducah Gaseous Diffusion Plant

    International Nuclear Information System (INIS)

    Spent trichloroethylene (TCE), 1,1,1-trichloroethane (TC-ane), and sludge are generated mainly as a result of vapor degreasing operations at the Paducah Gaseous Diffusion Plant (PGDP). Additionally, small quantities of spent chlorinated solvents are generated as a result of small parts cleanup. These wastes are listed hazardous wastes under Resource Conservation and Recovery Act (RCRA) regulations (40 CFR 261) and account for greater than 50% of the hazardous waste generated at PGDP. Additionally, some of the solvents become contaminated with uranium which classifies them as mixed waste for which no disposal method is currently available. TCE and TC-ane are both associated with potential health hazards and are subject to a number of environmental regulations. Due to health and environmental concerns and the desire to minimize mixed and hazardous waste generation, a study was initiated to identify nonchlorinated, less toxic degreasers, perform laboratory testing of the most promising alternatives, and initiate field testing to determine if alternate degreasers present operational problems. The degreaser that cleaned and protected metal surfaces best was an all-purpose, water-based, hard surface cleaner consisting of biodegradable synthetic detergents, inorganic builders, and a glycol ether solvent. Additionally, this product was free-rinsing and did not leave any contaminants that would react with commonly used process gases. This product is recommended as a replacement for chlorinated solvents for many degreasing operations at PGDP

  17. A study of chlorinated solvent contamination of the aquifers of an industrial area in central Italy: a possibility of bioremediation

    Directory of Open Access Journals (Sweden)

    FEDERICA eMATTEUCCI

    2015-09-01

    Full Text Available Perchloroethene, Trichloroethene, and other chlorinated solvents are widespread groundwater pollutants. They form Dense Non Aqueous Phase Liquids (DNAPLs that sink through permeable groundwater aquifers until non-permeable zone is reached. In Italy there are many situations of serious contamination of groundwater that might compromise their use in industry, agriculture, private, as the critical case of a Central Italy valley located in the province of Teramo (Val Vibrata, characterized by a significant chlorinated solvents contamination. Data from the various monitoring campaigns that have taken place over time were collected, and new samplings were carried out, resulting in a complete database. The data matrix was processed with a multivariate statistic analysis (in particular Principal Components Analysis, PCA and was then imported into Geographic Information System (GIS, to obtain a model of the contamination. A microcosm anaerobic study was utilized to assess the potential for in situ natural or enhanced bioremediation. Most of the microcosms were positive for dechlorination, particularly those inoculated with a mineral medium. This indicate the presence of an active native dechlorinating population in the subsurface, probably inhibited by co-contaminants in the groundwater, or more likely by the absence or lack of nutritional factors. Among the tested electron donors (i.e., yeast extract, lactate, and butyrate lactate and butyrate enhanced dechlorination of chlorinated compounds. PCA and GIS studies allowed delimiting the contamination; the microcosm study helped to identify the conditions to promote the bioremediation of the area.

  18. A newly isolated organic solvent tolerant Staphylococcus saprophyticus M36 produced organic solvent-stable lipase.

    Science.gov (United States)

    Fang, Yaowei; Lu, Zhaoxin; Lv, Fengxia; Bie, Xiaomei; Liu, Shu; Ding, Zhongyang; Xu, Weifeng

    2006-12-01

    Thirty-eight high lipase activity strains were isolated from soil, seawater, and Brassica napus. Among them, a novel organic solvent tolerant bacterium (strain M36) was isolated from the seawater in Jiangsu, China. Isolate M36 was able to grow at high concentration of benzene or toluene up to 40% (vol/vol), and later identified as Staphylococcus saprophyticus by biochemical test and 16s ribosomal DNA sequence. No work on Staphylococcus producing lipase with organic solvent tolerance has been reported so far. The lipase of strain M36 whose activity in liquid medium was 42 U mL(-1) at 24-h incubation time was stable in the presence of 25% (vol/vol) p-xylene, benzene, toluene, and hexane.

  19. Multiple Lines Of Evidence Supporting Natural Attenuation: Lines Of Inquiry Supporting Monitored Natural Attenuation And Enhanced Attenuatin Of Chlorinated Solvents

    Energy Technology Data Exchange (ETDEWEB)

    Vangelas, Karen; Widemeirer, T. H.; Barden, M.J.; Dickson, W. Z.; Major, David

    2004-12-31

    The Department of Energy (DOE) is sponsoring an initiative to facilitate efficient, effective and responsible use of Monitored Natural Attenuation (MNA) and Enhanced Attenuation (EA) for chlorinated solvents. This Office of Environmental Management (EM) ''Alternative Project,'' focuses on providing scientific and policy support for MNA/EA. A broadly representative working group of scientists supports the project along with partnerships with regulatory organizations such as the Interstate Technology Regulatory Council (ITRC) and the United States Environmental Protection Agency (USEPA). The initial product of the technical working group was a summary report that articulated the conceptual approach and central scientific tenants of the project, and that identified a prioritized listing of technical targets for field research. This report documented the process in which: (1) scientific ground rules were developed, (2) lines of inquiry were identified and then critically evaluated, (3) promising applied research topics were highlighted in the various lines of inquiry, and (4) these were discussed and prioritized. The summary report will serve as a resource to guide management and decision making throughout the period of the subject MNA/EA Alternative Project. To support and more fully document the information presented in the summary report, the DOE is publishing a series of supplemental documents that present the full texts from the technical analyses within the various lines of inquiry (see listing). The following report--documenting our evaluation of the state of the science for the lines of evidence for supporting decision-making for MNA--is one of those supplemental documents.

  20. Three-dimensional density-dependent flow and multicomponent reactive transport modeling of chlorinated solvent oxidation by potassium permanganate

    Science.gov (United States)

    Henderson, Thomas H.; Mayer, K. Ulrich; Parker, Beth L.; Al, Tom A.

    2009-05-01

    A popular method for the treatment of aquifers contaminated with chlorinated solvents is chemical oxidation based on the injection of potassium permanganate (KMnO 4). Both the high density (1025 gL - 1 ) and reactivity of the treatment solution influence the fate of permanganate (MnO 4) in the subsurface and affect the degree of contaminant treatment. The MIN3P multicomponent reactive transport code was enhanced to simulate permanganate-based remediation, to evaluate the pathways of MnO 4 utilization, and to assess the role of density contrasts for the delivery of the treatment solution. The modified code (MIN3P-D) provides a direct coupling between density-dependent fluid flow, solute transport, contaminant treatment, and geochemical reactions. The model is used to simulate a field trial of TCE oxidation in a sandy aquifer that is underlain by an aquitard. Three-dimensional simulations are conducted for a coupled reactive system comprised of ten aqueous components, two mineral phases, TCE (dissolved, adsorbed, and NAPL), reactive organic matter, and including ion exchange reactions. Model parameters are constrained by literature data and a detailed data set from the field site under investigation. The general spatial and transient evolution in observed concentrations of the oxidant, dissolved TCE, and reaction products are adequately reproduced by the simulations. The model elucidates the important role of density-induced flow and transport on the distribution of the treatment solution into NAPL containing regions located at the aquifer-aquitard interface. Model results further suggest that reactions that do not directly affect the stability of MnO 4 have a negligible effect on solution density and MnO 4 delivery.

  1. Combining non-invasive techniques for delimitation and monitoring of chlorinated solvents in groundwater

    Science.gov (United States)

    Sparrenbom, Charlotte; Åkesson, Sofia; Hagerberg, David; Dahlin, Torleif; Holmstrand, Henry; Johansson, Sara

    2016-04-01

    groundwater sampling provide reference data within the project and for calibrating interpretations. In our studies, we show the results from DCIP measurements from two different areasin sothern Sweden with chlorinated solvent contamination. From one of the areas, a pilot test on stimulation reductive dechlorination has been carried out and the treated area reveals sharp anomalies in the DCIP response. Time lapse measurements show changes within the stimulated area and this could be used to follow remediation changes and i.e. groundwater quality changes. Tests with DCIP time lapse are also carried out in the second area together with multiple CSIA analyses of groundwater samples and ongoing is the planning for the gas samples. Evaluation of the possible uses, benefits and limitations of the technique for monitoring changes and delimit polluted areas to be able to monitor and follow groundwater quality changes is ongoing.

  2. ASCORBIC ACID REDUCTION OF ACTIVE CHLORINE PRIOR TO DETERMINING AMES MUTAGENICITY OF CHLORINATED NATURAL ORGANIC MATTER (NOM)

    Science.gov (United States)

    Many potable water disinfection byproducts (DBPs) that result from the reaction of natural organic matter (NOM) with oxidizing chlorine are known or suspected to be carcinogenic and mutagenic. The Ames assay is routinely used to assess an overall level of mutagenicity for all com...

  3. IMPROVED DOWN-HOLE CPT TOOLS FOR THE DETECTION OF CHLORINATED SOLVENTS; FINAL

    International Nuclear Information System (INIS)

    Conventional soil and groundwater sampling procedures present many opportunities for loss of volatile organic compounds (VOC) by exposing sample media to the atmosphere during transfers between sampling devices and containers, ultimately affecting the quality of the analytical results. Inaccurate characterization data often leads to improperly designed remedial systems that slow the clean-up process and increase the cost. For these reasons, in situ methods for sample extraction and real time analysis provide attractive alternatives to conventional sampling and analysis. Under funding from the U.S. Department of Energy's Federal Energy Technology Center (FETC), the investigators continued development of a system that combines High Speed Gas Chromatography techniques with Cone Penetration Testing to achieve near-real time analysis of soils and groundwater for chlorinated and aromatic hydrocarbon contamination (PCE, TCE, BTEX) during site characterization. The system combines three new CPT tools with an up-hole analyzer. The Dynamic Thermal Desorption (DTD) probe provides the up-hole analyzer with continuously sampled soil gas, enhancing detection limits by heating the soil matrix during penetration to thermally desorb volatile organic contaminants. The CPT In Situ Purge Probe (CISP) purges a water sample in situ, transferring the purge gas up-hole for analysis. Alternatively, soil gas or purge gas from the DTD probe or the CISP can be diverted to a Downhole Trap Module (DTM), which traps contaminants on conventional trap media for later analysis in a fixed laboratory. While the effectiveness of the CISP was hampered by the tendency of fine grained materials to clog its sample inlet filter, the DTD probe and the DTM were demonstrated to perform their intended functions well

  4. IMPROVED DOWN-HOLE CPT TOOLS FOR THE DETECTION OF CHLORINATED SOLVENTS

    Energy Technology Data Exchange (ETDEWEB)

    Martin L. Gildea; Stephen P. Farrington, P.E.; Wesley L. Bratton, Ph.D., PE

    1998-09-01

    Conventional soil and groundwater sampling procedures present many opportunities for loss of volatile organic compounds (VOC) by exposing sample media to the atmosphere during transfers between sampling devices and containers, ultimately affecting the quality of the analytical results. Inaccurate characterization data often leads to improperly designed remedial systems that slow the clean-up process and increase the cost. For these reasons, in situ methods for sample extraction and real time analysis provide attractive alternatives to conventional sampling and analysis. Under funding from the U.S. Department of Energy's Federal Energy Technology Center (FETC), the investigators continued development of a system that combines High Speed Gas Chromatography techniques with Cone Penetration Testing to achieve near-real time analysis of soils and groundwater for chlorinated and aromatic hydrocarbon contamination (PCE, TCE, BTEX) during site characterization. The system combines three new CPT tools with an up-hole analyzer. The Dynamic Thermal Desorption (DTD) probe provides the up-hole analyzer with continuously sampled soil gas, enhancing detection limits by heating the soil matrix during penetration to thermally desorb volatile organic contaminants. The CPT In Situ Purge Probe (CISP) purges a water sample in situ, transferring the purge gas up-hole for analysis. Alternatively, soil gas or purge gas from the DTD probe or the CISP can be diverted to a Downhole Trap Module (DTM), which traps contaminants on conventional trap media for later analysis in a fixed laboratory. While the effectiveness of the CISP was hampered by the tendency of fine grained materials to clog its sample inlet filter, the DTD probe and the DTM were demonstrated to perform their intended functions well.

  5. Dispersion and separation of nanostructured carbon in organic solvents

    Science.gov (United States)

    Landi, Brian J. (Inventor); Raffaelle, Ryne P. (Inventor); Ruf, Herbert J. (Inventor); Evans, Christopher M. (Inventor)

    2011-01-01

    The present invention relates to dispersions of nanostructured carbon in organic solvents containing alkyl amide compounds and/or diamide compounds. The invention also relates to methods of dispersing nanostructured carbon in organic solvents and methods of mobilizing nanostructured carbon. Also disclosed are methods of determining the purity of nanostructured carbon.

  6. Uranium extraction from colofanite via organic solvents

    International Nuclear Information System (INIS)

    This work describes the use of pure or combined extractants dissolved in organic solvents for quantitative uranium recovery from colofanite, a fluoroapatite ore, from Itataia, Santa Quiteria, Ceara, Brazil. This ore contains the highest brazilian uranium reserve. The metal is associated to phosphate species. The ore is digested with sulfuric acid (wet process), producing phosphoric acid, which is used for manufacturing of fertilizers and animal food. >From the acid leaching, some systems for uranium recovery were tested. Among them, PC88A (2-ethyl-hexyl phosphonic acid, mono-2-ethyl-hexyl ester) 40% vol. and DEHPA (di(2-ethyl-hexyl)phosphoric acid) 40% vol. in kerosene presented the highest values for the distribution coefficient (D) for uranium. When synergistic systems were employed, the best results were obtained for DEHPA 40%vol. + PC88A 40%vol. and DEHPA 40% vol. + TOPO (trioctylphosphine oxide) 5% vol. in kerosene. 15% wt/v sodium carbonate was the best medium for uranium stripping and separation from iron, the main interfering element. Uranium was precipitated as sodium diuranate by adding sodium hydroxide (5,0 mol L-1). Thorium in the raffinate was extracted by TOPO (0,1% vol.) in cyclohexane. The radioactivity level of the final aqueous waste is similar to natural background, according to CNEN-NE 6.05 Norm. After neutralization, the solid can be co-processed, according to the Directory 264 from the National Brazilian Environmental Council (CONAMA), whereas the treated effluent can be discarded according to the Directory 357 from CONAMA. (author)

  7. A hand-portable instrument system for the real-time analysis of chlorinated organic compound contamination

    International Nuclear Information System (INIS)

    Working with the DOE Morgantown Energy Technology Center, Transducer Research, Inc. (TRI) recently developed a new chemical monitor which responds selectively to vapors of chlorinated solvents. No response is observed with common hydrocarbon organic compounds such as BTXs (benzene, toluene, xylene) or POLs (petroleum, oil, lubricants), and in fact, no nonhalogen containing chemical has been identified which induces a measurable response. This instrument, the RCL MONITOR, was designed to analyze individual samples or monitor an area with automated repetitive analyses. Vapor levels between 0 and 500 ppm can be determined in 90 s with a lower detection limit of 0.2 ppm using the hand-portable instrument. In addition to the development of the RCL MONITOR, advanced sampler systems are being developed to: (1) extend the dynamic range of the instrument through autodilution of the vapor and (2) allow chemical analyses to be performed on groundwater with a unique closed-loop sampler. When interfaced to the samplers, the RCL MONITOR is capable of measuring chlorinated solvent contamination in the vapor phase up to 5,000 ppm and in water and other condensed media from 10 to over 10,000 ppbwt. The performance of RCL MONITOR was demonstrated at several DOE facilities and applications have been identified in which the selective and sensitive measurement and monitoring of chlorinated hydrocarbons is essential. Case studies are currently underway at DOE Hanford and the Idaho National Engineering Laboratory

  8. Method for Selection of Solvents for Promotion of Organic Reactions

    DEFF Research Database (Denmark)

    Gani, Rafiqul; Jiménez-González, Concepción; Constable, David J.C.

    2005-01-01

    A method to select appropriate green solvents for the promotion of a class of organic reactions has been developed. The method combines knowledge from industrial practice and physical insights with computer-aided property estimation tools for selection/design of solvents. In particular, it employs...... estimates of thermodynamic properties to generate a knowledge base of reaction, solvent and environment related properties that directly or indirectly influence the rate and/or conversion of a given reaction. Solvents are selected using a rules-based procedure where the estimated reaction-solvent properties...... and the solvent-environmental properties guide the decision making process. The current method is applicable only to organic reactions occurring in the liquid phase. Another gas or solid phase, which may or may not be at equilibrium with the reacting liquid phase, may also be present. The objective of this method...

  9. Formation of disinfection byproducts upon chlorine dioxide preoxidation followed by chlorination or chloramination of natural organic matter.

    Science.gov (United States)

    Yang, Xin; Guo, Wanhong; Lee, Wontae

    2013-06-01

    Chlorine dioxide (ClO2) is often used as an oxidant to remove taste, odor and color during water treatment. Due to the concerns of the chlorite formation, chlorination or chloramination is often applied after ClO2 preoxidation. We investigated the formation of regulated and emerging disinfection byproducts (DBPs) in sequential ClO2-chlorination and ClO2-chloramination processes. To clarify the relationship between the formation of DBPs and the characteristics of natural organic matter (NOM), changes in the properties of NOM before and after ClO2 oxidation were characterized by fluorescence, Fourier transform infrared spectroscopy (FTIR), and size and resin fractionation techniques. ClO2 preoxidation destroyed the aromatic and conjugated structures of NOM and transformed large aromatic and long aliphatic chain organics to small and hydrophilic organics. Treatment with ClO2 alone did not produce significant amount of trihalomethanes (THMs) and haloacetic acids (HAAs), but produced chlorite. ClO2 preoxidation reduced THMs, HAAs, haloacetonitriles (HANs) and chloral hydrate (CH) during subsequent chlorination, but no reduction of THMs was observed during chloramination. Increasing ClO2 doses enhanced the reduction of most DBPs except halonitromethanes (HNMs) and haloketones (HKs). The presence of bromide increased the formation of total amount of DBPs and also shifted DBPs to more brominated ones. Bromine incorporation was higher in ClO2 treated samples. The results indicated that ClO2 preoxidation prior to chlorination is applicable for control of THM, HAA and HAN in both pristine and polluted waters, but chlorite formation is a concern and HNMs and HKs are not effectively controlled by ClO2 preoxidation.

  10. Psychomotor Effects of Mixed Organic Solvents on Rubber Workers

    Directory of Open Access Journals (Sweden)

    O Aminian

    2014-04-01

    Full Text Available Background: Exposure to organic solvents is common among workers.Objective: To assess neurobehavioral effects of long-term exposure to organic solvents among rubber workers in Tehran, Iran.Methods: Across-sectional study was conducted on 223 employees of a rubber industry. The participants completed a data collection sheet on their occupational and medical history, and demographic characteristics including age, work experience, education level; they performed 6 psychiatric tests on the neurobehavioral core test battery (NCTB that measure simple reaction time, short-term memory (digit span, Benton, eye-hand coordination (Purdue pegboard, pursuit aiming, and perceptual speed (digit symbol.Results: Workers exposed and not exposed to organic solvents had similar age and education distribution. The mean work experience of the exposed and non-exposed workers was 5.9 and 4.4 years, respectively. The exposed workers had a lower performance compared to non-exposed workers in all psychomotor tests. After controlling for the confounders by logistic regression analysis, it was found that exposure to organic solvents had a significant effect on the results of digit symbols, digit span, Benton, aiming, and simple reaction time tests. No significant effect was observed in pegboard test.Conclusion: Occupational exposure to organic solvent can induce subtle neurobehavioral changes among workers exposed to organic solvents; therefore, periodical evaluation of the central nervous system by objective psychomotor tests is recommended among those who are chronically exposed to organic solvents.

  11. NMR microscopy of tissue in organic and mixed solvents

    Directory of Open Access Journals (Sweden)

    Macura Slobodan

    2013-01-01

    Full Text Available We propose to use organic and mixed solvents for nuclear magnetic resonance microscopy of fixed tissue as a means for improving image information content. NMR properties of some standard solvents (methanol, acetone, DMSO and solvents in use for tissue processing in pathology (xylenes, paraffin, ‘Clearify’ have been measured, reviewed, and analyzed. It was found that DMSO and paraffin are very useful solvents that provide images of better quality than those obtained in water (neutralized formalin buffer. This is illustrated on the formalin fixed mouse brain sections imaged at 16.4 teslas (700 MHz.

  12. Solvent Selection for Recrystallization: An Undergraduate Organic Experiment.

    Science.gov (United States)

    Baumann, Jacob B.

    1979-01-01

    This experiment develops the students' ability to carry out a simple recrystallization effectively, and demonstrates how a solvent may be selected or rejected for the recrystallization of a specific organic compound. (Author/BB)

  13. Electrokinetic-enhanced bioaugmentation for remediation of chlorinated solvents contaminated clay

    OpenAIRE

    Mao, Xuhui; Wang, James; Ciblak, Ali; Cox, Evan E.; Riis, Charlotte; Terkelsen, Mads; Gent, David B.; Alshawabkeh, Akram N

    2012-01-01

    Successful bioremediation of contaminated soils is controlled by the ability to deliver bioremediation additives, such as bacteria and/or nutrients, to the contaminated zone. Because hydraulic advection is not practical for delivery in clays, electrokinetic (EK) injection is an alternative for efficient and uniform delivery of bioremediation additive into low-permeability soil and heterogeneous deposits. EK–enhanced bioaugmentation for remediation of clays contaminated with chlorinated solven...

  14. Enhanced bioremediation as a cost effective approach following thermally enhanced soil vapour extraction for sites requiring remediation of chlorinated solvents - 16296

    International Nuclear Information System (INIS)

    Thermally enhanced bioremediation can be a more cost-effective alternative to full scale in-situ thermal treatment especially for sites contaminated with chlorinated solvents, where reductive dechlorination is or might be a dominant biological step. The effect of Thermally Enhanced Soil Vapour Extraction (TESVE) on indigenous microbial communities and the potential for subsequent biological polishing of chlorinated solvents was investigated in field trials at the Western Storage Area (WSA) - RSRL (formerly United Kingdom Atomic Energy Authority - UKAEA) Oxfordshire, UK. The WSA site had been contaminated with various chemicals including mineral oil, chloroform, trichloroethane (TCA), carbon tetrachloride and tetrachloroethene (PCE). The contamination had affected the unsaturated zone, groundwater in the chalk aquifer and was a continuing source of groundwater contamination below the WSA. During TESVE the target treatment zone was heated to above the boiling point of water increasing the degree of volatilization of contaminants of concern (CoC), which were mobilised and extracted in the vapour phase. A significant reduction of concentrations of chlorinated solvent in the unsaturated zone was achieved by the full-scale application of TESVE - In Situ Thermal Desorption (ISTD) technology. The rock mass temperature within target treatment zone remained in the range of 35 deg. - 44 deg. C, 6 months after cessation of heating. The concentration of chlorinated ethenes and other CoC were found to be significantly lower adjacent to the thermal treatment area and 1 to 2 orders of magnitude lower within the thermal treatment zone. Samples were collected within and outside the thermal treatment zone using BioTrapsR (passive, in- situ microbial samplers) from which the numbers of specific bacteria were measured using quantitative polymerase chain reaction (qPCR) methods of analysis. High populations of reductive de-chlorinators such as Dechalococcoides spp. and Dehalobacter spp

  15. Self-healing Microencapsulation of Biomacromolecules without Organic Solvents**

    Science.gov (United States)

    Reinhold, Samuel E.; Desai, Kashappa-Goud H.; Zhang, Li; Olsen, Karl F.

    2012-01-01

    Microencapsulation of biomacromolecules in PLGA is routinely performed with organic solvent through multiple complex steps deleterious to the biomacromolecule. The new self-healing based PLGA microencapsulation obviates micronization- and organic solvent-induced protein damage, provides very high encapsulation efficiency, exhibit stabilization and slow release of labile tetanus protein antigen, and provides long-term testosterone suppression in rats following a single injection of encapsulated leuprolide. PMID:23011773

  16. Background Noise Contributes to Organic Solvent Induced Brain Dysfunction

    Directory of Open Access Journals (Sweden)

    O’neil W. Guthrie

    2016-01-01

    Full Text Available Occupational exposure to complex blends of organic solvents is believed to alter brain functions among workers. However, work environments that contain organic solvents are also polluted with background noise which raises the issue of whether or not the noise contributed to brain alterations. The purpose of the current study was to determine whether or not repeated exposure to low intensity noise with and without exposure to a complex blend of organic solvents would alter brain activity. Female Fischer344 rats served as subjects in these experiments. Asynchronous volume conductance between the midbrain and cortex was evaluated with a slow vertex recording technique. Subtoxic solvent exposure, by itself, had no statistically significant effects. However, background noise significantly suppressed brain activity and this suppression was exacerbated with solvent exposure. Furthermore, combined exposure produced significantly slow neurotransmission. These abnormal neurophysiologic findings occurred in the absence of hearing loss and detectable damage to sensory cells. The observations from the current experiment raise concern for all occupations where workers are repeatedly exposed to background noise or noise combined with organic solvents. Noise levels and solvent concentrations that are currently considered safe may not actually be safe and existing safety regulations have failed to recognize the neurotoxic potential of combined exposures.

  17. Ozonated water and chlorine effects on the antioxidant properties of organic and conventional broccoli during postharvest

    OpenAIRE

    Giuseppina Pace Pereira Lima; Tatiana Marquini Machado; Luciana Manoel de Oliveira; Luciana da Silva Borges; Valber de Albuquerque Pedrosa; Paola Vanzani; Fabio Vianello

    2014-01-01

    There is growing interest in studies on sanitizers other than chlorine that can maintain the quality of organic products without affecting their phytochemical content. The effects of using chlorinated and ozonized water treatments, as sanitizing procedures, on the post-harvest quality of organic and conventional broccoli (Brassica oleracea L.) cv. Italica was evaluated. The biochemical parameters (chlorophyll, polyphenols, flavonoids, vitamin C and antioxidant capacity) of the broccoli sample...

  18. Effects of assimilable organic carbon and free chlorine on bacterial growth in drinking water.

    Directory of Open Access Journals (Sweden)

    Xiaolu Liu

    Full Text Available Assimilable organic carbon (AOC is one of the most important factors affecting the re-growth of microorganisms in drinking water. High AOC concentrations result in biological instability, but disinfection kills microbes to ensure the safety of drinking water. Free chlorine is an important oxidizing agent used during the disinfection process. Therefore, we explored the combined effects of AOC and free chlorine on bacterial growth in drinking water using flow cytometry (FCM. The initial AOC concentration was 168 μg.L(-1 in all water samples. Without free chlorine, the concentrations of intact bacteria increased but the level of AOC decreased. The addition of sodium hypochlorite caused an increase and fluctuation in AOC due to the oxidation of organic carbon. The concentrations of intact bacteria decreased from 1.1 × 10(5 cells.mL(-1 to 2.6 × 10(4 cells.mL(-1 at an initial free chlorine dose of 0.6 mg.L(-1 to 4.8 × 10(4 cells.mL(-1 at an initial free chlorine dose of 0.3 mg.L(-1 due to free chlorine originating from sodium hypochlorite. Additionally, free chlorine might be more obviously affected AOC concentrations than microbial growth did. These results suggested that AOC and free chlorine might have combined effects on microbial growth. In this study, our results showed concentrations determined by FCM were higher than those by HPC, which indicated that some E. coli detected by FCM might not be detected using HPC in drinking water. The level of free chlorine might restrain the consumption of AOC by inhibiting the growth of E. coli; on the other hand, chlorination might increase the level of AOC, thereby increase the potential for microbial growth in the drinking water network.

  19. Affinity Solvents for Intensified Organics Extraction: Development Challenges and Prospects

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    In most organics extraction processes, the commonly used solvents employ solely physical interactions. Therefore, for the recovery and purification of products from complex mixtures, the selectivity and/or capacity of classical solvents towards the desired solutes is usually insufficient, enforcing the need for complex and thus expensive separation schemes. Significant simplification and cost-reduction can be achieved when affinity solvents would be available that are able to recognize the solutes of interest by their molecular structure. The main development challenges to establish such affinity solvents are: Selection and incorporation of molecular recognition and complexation capabilities; Evaluation of extraction capabilities; Efficient recovery and recycling of the affinity solvents; Implementation in industrial extraction equipment. This paper presents how these development challenges are addressed at the University of Twente, going all the way from affinity solvent design and synthesis, via high throughput screening and characterization up to pilot plant evaluation. Essential in the successful development of affinity solvents are structural cooperations with molecular chemists and custom synthesis companies for their design and synthesis. The various aspects are illustrated by several examples where newly developed environmentally benign affinity solvents appeared able to create major breakthroughs. The applications addressed involve oxygenates, sugars, and pharmaceutical ingredients, such as optical isomers and biomolecules.

  20. Limitations and feasibility of the land disposal of organic solvent-contaminated wastes

    Science.gov (United States)

    Roy, W. R.; Griffin, R. A.; Mitchell, J. K.; Mitchell, R. A.

    1989-05-01

    The limitations and feasibility of the land disposal of solid wastes containing organic solvents and refrigerants (chlorinated fluorocarbons) were investigated by evaluating the attenuation capacity of a hypothetical waste-disposal site by numerical modeling. The basic theorem of this approach was that the land disposal of wastes would be environmentally acceptable if subsurface attenuation reduced groundwater concentrations of organic compounds to concentrations that were less than health-based, water-quality criteria. Computer simulations indicated that the predicted concentrations of 13 of 33 organic compounds in groundwater would be less than their health-based criteria. Hence, solid wastes containing these compounds could be safely disposed at the site. The attenuation capacity of the site was insufficient to reduce concentrations of four compounds to safe levels without limiting the amount of mass available to leach into groundwater. Threshold masses based on time-dependent migration simulations were estimated for these compounds. The remaining 16 compounds, which consisted mainly of chlorinated hydrocarbons and fluorocarbons could not be safely landfilled without severe restrictions on the amounts disposed. These organic compounds were candidates to ban from land disposal.

  1. Measurement of oxygen transfer from air into organic solvents

    DEFF Research Database (Denmark)

    Ramesh, Hemalata; Mayr, Torsten; Hobisch, Mathias;

    2016-01-01

    Background:The use of non-aqueous organic media is becoming increasingly important in many biotechnological applications in order to achieve process intensification. Such media can be used for example to directly extract poorly water-soluble toxic products from fermentations. Likewise many...... measurements in organic solvents has also been demonstrated, paving the way for new opportunities in process control....

  2. Determination of chlorinated solvents in industrial water and wastewater by DAI-GC-ECD

    Energy Technology Data Exchange (ETDEWEB)

    Tobiszewski, Marek; Namiesnik, Jacek [Gdansk University of Technology (GUT), Department of Analytical Chemistry, Chemical Faculty, Gdansk (Poland)

    2011-04-15

    A very simple and quick analytical method, based on direct aqueous injection, for determination of halogenated solvents in refinery water and wastewater, is described. There is a need to determine halogenated solvents in refinery water streams, because they may originate from several processes. There is also a need to develop methods enabling VOX to be determined in samples containing oil fractions. The method described enables simultaneous determination of 26 compounds with low detection limits (sub-{mu}g L{sup -1}) and excellent precision, especially for highly halogenated solvents. The matrix effects of four types of sample were evaluated - the method seemed to be relatively insensitive to variations in matrix composition. Deuterated 1,2-dichloroethane was used as internal standard and surrogate compound in quantitative analysis; application of isotopically labelled compounds is rarely reported when non-mass spectrometric detectors are used for analysis. Analysis of real samples showed that the most frequently detected compounds were dichloromethane and 1,2-dichloroethane. (orig.)

  3. Alternatives to Organic Solvents in Industrial Cleaning Processes

    DEFF Research Database (Denmark)

    Jacobsen, Thomas

    1998-01-01

    industry, and vehicle repair and maintenance. There are, however, other elements that influence the possibility to substitute. The requirements to the resulting surface, depending on the following treatment of the surface. The character of the soilings to be removed. The possible presence of other...... cleaning agents in offset printing companies instead of volatile, toxic organic solvents. The present study is based on a project with the aim of defining other industrial processes, where organic solvents used for cleaning or degreasing can be replaced by non-volatile, low-toxic products, which are based...... on esters from fatty acids of vegetable origin (vegetable esters - VE).The study indicates that industrial cleaning/degreasing with organic solvents may be substituted with VEs on metal surfaces and on some coated surfaces, in manufacture of paints and inks, use of paints, use of inks (printing), metal...

  4. Technology status report: Off-gas treatment technologies for chlorinated volatile organic compound air emissions

    Energy Technology Data Exchange (ETDEWEB)

    Rossabi, J.; Haselow, J.S.

    1992-04-15

    The purpose of this document is to review technologies for treatment of air streams that contain chlorinated volatile organic compounds (CVOCS) and to describe a Department of Energy Office of Technology Development program that is planned to demonstrate innovative technologies for the abatement of CVOC emissions. This report describes the first phase of testing of off-gas treatment technologies. At least one more phase of testing is planned. Guidance for the preparation of this document was provided by a predecisional draft outline issued by the Department of Energy's Office of Technology Development. The report is intended to evaluate the technical and regulatory aspects, public acceptance, and estimated costs of technologies selected for development and testing. These technologies are compared to currently practiced or baseline methods for treatment of CVOC-laden airstreams. A brief overview is provided rather than detailed cost and data comparisons because many of these technologies have not yet been field tested. A description of other promising technologies for the treatment of CVOC emissions is also included. Trichloroethylene (TCE) and perchloroethylene (PCE) were used for industrial cleaning and solvent applications for several decades. These chemicals can be classified as CVOCS. As a result of past standard disposal practices, these types of compounds are persistent groundwater and soil contaminants throughout the United States and the Department of Energy Complex.

  5. Technology status report: Off-gas treatment technologies for chlorinated volatile organic compound air emissions

    Energy Technology Data Exchange (ETDEWEB)

    Rossabi, J.; Haselow, J.S.

    1992-04-15

    The purpose of this document is to review technologies for treatment of air streams that contain chlorinated volatile organic compounds (CVOCS) and to describe a Department of Energy Office of Technology Development program that is planned to demonstrate innovative technologies for the abatement of CVOC emissions. This report describes the first phase of testing of off-gas treatment technologies. At least one more phase of testing is planned. Guidance for the preparation of this document was provided by a predecisional draft outline issued by the Department of Energy`s Office of Technology Development. The report is intended to evaluate the technical and regulatory aspects, public acceptance, and estimated costs of technologies selected for development and testing. These technologies are compared to currently practiced or baseline methods for treatment of CVOC-laden airstreams. A brief overview is provided rather than detailed cost and data comparisons because many of these technologies have not yet been field tested. A description of other promising technologies for the treatment of CVOC emissions is also included. Trichloroethylene (TCE) and perchloroethylene (PCE) were used for industrial cleaning and solvent applications for several decades. These chemicals can be classified as CVOCS. As a result of past standard disposal practices, these types of compounds are persistent groundwater and soil contaminants throughout the United States and the Department of Energy Complex.

  6. Mobility of organic solvents in water-saturated soil materials

    Science.gov (United States)

    Roy, W.R.; Griffin, R.A.

    1985-01-01

    This investigation presents an analysis of the mobility of 37 organic solvents in saturated soil-water systems, focusing on adsorption phenomena at the solid-liquid interface This analysis was made, in part, by applying predictive expressions that estimate the potential magnitude of adsorption by soil materials Of the 37 solvents considered, 19 were classified as either "very highly mobile" or "highly mobile" and, thus, would have little tendency to be retained by soils to a significant extent, 12 were considered to have medium mobility and 6 low mobility None of these solvents were in the immobile class The limited information available indicates that these predictive expressions yield satisfactory first approximations of the magnitude of adsorption of these solvents by soil materials ?? 1985 Springer-Verlag New York Inc.

  7. Phase Behavior of Mixtures of Ionic Liquids and Organic Solvents

    DEFF Research Database (Denmark)

    Abildskov, Jens; Ellegaard, Martin Dela; O’Connell, J.P.

    2010-01-01

    A corresponding-states form of the generalized van der Waals equation, previously developed for mixtures of an ionic liquid and a supercritical solute, is here extended to mixtures including an ionic liquid and a solvent (water or organic). Group contributions to characteristic parameters...... are implemented, leading to an entirely predictive method for densities of mixed compressed ionic liquids. Quantitative agreement with experimental data is obtained over wide ranges of conditions. Previously, the method has been applied to solubilities of sparingly soluble gases in ionic liquids and in organic...... solvents. Here we show results for heavier and more-than-sparingly solutes such as carbon dioxide and propane in ionic liquids....

  8. Highly chlorinated unintentionally produced persistent organic pollutants generated during the methanol-based production of chlorinated methanes: A case study in China.

    Science.gov (United States)

    Zhang, Lifei; Yang, Wenlong; Zhang, Linli; Li, Xiaoxiu

    2015-08-01

    The formation of unintentionally produced persistent organic pollutants (POPs) may occur during various chlorination processes. In this study, emissions of unintentionally produced POPs during the methanol-based production of chlorinated methanes were investigated. High concentrations of highly chlorinated compounds such as decachlorobiphenyl, octachloronaphthalene, octachlorostyrene, hexachlorobutadiene, hexachlorocyclopentadiene, hexachlorobenzene, and pentachlorobenzene were found in the carbon tetrachloride byproduct of the methanol-based production of chlorinated methanes. The total emission amounts of hexachlorocyclopentadiene, hexachlorobutadiene, polychlorinated benzenes, polychlorinated naphthalenes, octachlorostyrene, and polychlorinated biphenyls released during the production of chlorinated methanes in China in 2010 were estimated to be 10080, 7350, 5210, 427, 212, and 167 kg, respectively. Moreover, polychlorinated dibenzo-p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs) were formed unintentionally during chlorinated methanes production, the emission factor for PCDDs/DFs was 364 μg toxic equivalency quotient (TEQ) t(-1) product for residues, which should be added into the UNEP toolkit for updating. It was worth noting that a high overall toxic equivalency quotient from polychlorinated naphthalenes and PCDDs/DFs was generated from the chlorinated methanes production in China in 2010. The values reached 563 and 32.8 g TEQ, respectively. The results of the study indicate that more research and improved management systems are needed to ensure that the methanol-based production of chlorinated methanes can be achieved safely. PMID:25777670

  9. Combined nano-biotechnology for in-situ remediation of mixed contamination of groundwater by hexavalent chromium and chlorinated solvents.

    Science.gov (United States)

    Němeček, Jan; Pokorný, Petr; Lhotský, Ondřej; Knytl, Vladislav; Najmanová, Petra; Steinová, Jana; Černík, Miroslav; Filipová, Alena; Filip, Jan; Cajthaml, Tomáš

    2016-09-01

    The present report describes a 13month pilot remediation study that consists of a combination of Cr(VI) (4.4 to 57mg/l) geofixation and dechlorination of chlorinated ethenes (400 to 6526μg/l), achieved by the sequential use of nanoscale zerovalent iron (nZVI) particles and in situ biotic reduction supported by whey injection. The remediation process was monitored using numerous techniques, including physical-chemical analyses and molecular biology approaches which enabled both the characterization of the mechanisms involved in pollutant transformation and the description of the overall background processes of the treatment. The results revealed that nZVI was efficient toward Cr(VI) by itself and completely removed it from the groundwater (LOQ 0.05mg/l) and the subsequent application of whey resulted in a high removal of chlorinated ethenes (97 to 99%). The persistence of the reducing conditions, even after the depletion of the organic substrates, indicated a complementarity between nZVI and the whey phases in the combined technology as the subsequent application of whey phase partially assisted the microbial regeneration of the spent nZVI by promoting its reduction into Fe(II), which further supported remediation conditions at the site. Illumina sequencing and the detection of functional vcrA and bvcA genes documented a development in the reducing microbes (iron-reducing, sulfate-reducing and chlororespiring bacteria) that benefited under the conditions of the site and that was probably responsible for the high dechlorination and/or Cr(VI) reduction. The results of this study demonstrate the feasibility and high efficiency of the combined nano-biotechnological approach of nZVI and whey application in-situ for the removal of Cr(VI) and chlorinated ethenes from the groundwater of the contaminated site. PMID:26850861

  10. Transitioning organic synthesis from organic solvents to water. What's your E Factor?

    Science.gov (United States)

    Lipshutz, Bruce H; Ghorai, Subir

    2014-08-01

    Traditional organic chemistry, and organic synthesis in particular, relies heavily on organic solvents, as most reactions involve organic substrates and catalysts that tend to be water-insoluble. Unfortunately, organic solvents make up most of the organic waste created by the chemical enterprise, whether from academic, industrial, or governmental labs. One alternative to organic solvents follows the lead of Nature: water. To circumvent the solubility issues, newly engineered "designer" surfactants offer an opportunity to efficiently enable many of the commonly used transition metal-catalyzed and related reactions in organic synthesis to be run in water, and usually at ambient temperatures. This review focuses on recent progress in this area, where such amphiphiles spontaneously self-aggregate in water. The resulting micellar arrays serve as nanoreactors, obviating organic solvents as the reaction medium, while maximizing environmental benefits.

  11. Transitioning organic synthesis from organic solvents to water. What's your E Factor?

    Science.gov (United States)

    Lipshutz, Bruce H.; Ghorai, Subir

    2014-01-01

    Traditional organic chemistry, and organic synthesis in particular, relies heavily on organic solvents, as most reactions involve organic substrates and catalysts that tend to be water-insoluble. Unfortunately, organic solvents make up most of the organic waste created by the chemical enterprise, whether from academic, industrial, or governmental labs. One alternative to organic solvents follows the lead of Nature: water. To circumvent the solubility issues, newly engineered “designer” surfactants offer an opportunity to efficiently enable many of the commonly used transition metal-catalyzed and related reactions in organic synthesis to be run in water, and usually at ambient temperatures. This review focuses on recent progress in this area, where such amphiphiles spontaneously self-aggregate in water. The resulting micellar arrays serve as nanoreactors, obviating organic solvents as the reaction medium, while maximizing environmental benefits. PMID:25170307

  12. [Generic method for determination of volatile organic solvents in cosmetics].

    Science.gov (United States)

    Da, Jing; Huang, Xianglu; Wang, Gangli; Cao, Jin; Zhang, Qingsheng

    2014-11-01

    A generic screening, confirmation and determination method was established based on 36 commonly used volatile organic solvents in cosmetics by headspace gas chromatography- mass spectrometry (GC-MS). This method included a database for pilot screening and identifi- cation of those solvents and their quantitative method. Pilot screening database was composed by two sections, one was household section built by two columns with opposite polarities (col- umn VF-1301 ms and DB-5 ms) using retention index in different column systems as qualitative parameter, and the other was NIST MS search version 2.0. Meanwhile, the determination method of the 36 volatile solvents was developed with GC-MS. Cosmetic samples were dissolved in water and transferred to a headspace vial. After 30 min equilibration at 60 °C, the samples were analyzed by GC-MS equipped with a capillary chromatographic column VF-1301 ms. The external calibration was used for quantification. The limits of detection were from 0.01 to 3.3 μg/g, and the recoveries were from 60.77% to 126.6%. This study provided a generic method for pilot screening, identification, and quantitation of volatile organic solvents in cosmetics, and may solve the problem that different analytical methods need to be developed for different targeted compounds and pilot screening for potential candidate solvent residues.

  13. INFLUENCE OF ORGANIC SOLVENTS ON WATER DISSOCIATION IN BIPOLAR MEMBRANE

    Directory of Open Access Journals (Sweden)

    Sheldeshov N. V.

    2015-12-01

    Full Text Available The article discusses results of experimental research of the influence of aprotic and proton solvents on reaction rate of water molecules dissociation in the bipolar membrane MB-1 by the method of electrochemical impedance frequency spectrum. It was discovered, that addition of organic component in aqueous solutions results in significant influence on the parameters of water dissociation in a bipolar region of the membrane. The reason for this influence is the reduction of the mass fraction of water in solution and, consequently, in a bipolar region of the membrane, which itself reduces the rate of the dissociation reaction. Another reason for the influence of the organic solvent is its effect on the network of hydrogen bonds existing in water and aqueous solutions. Depending on the nature of organic solvent and its concentration, the network of hydrogen bonds may be strengthened, or destroyed, thus facilitating removal of the proton involved in the reactions between water molecules and catalytic centers in cation-exchange and anion-exchange layer of bipolar membrane, or retarding removal of proton. This leads respectively to speed up or slow down the rate of dissociation in the bipolar region of the membrane, as well as changing the constants of the dissociation reaction of water. Introduction of organic solvent in solutions, which are in the contact with bipolar membrane, is a convenient method of investigating the role of solution composition on the rate of proton transfer between water molecules and catalytic centers in the membranes

  14. Peptide synthesis in neat organic solvents with novel thermostable proteases

    NARCIS (Netherlands)

    Toplak, Ana; Nuijens, Timo; Quaedflieg, Peter J L M; Wu, Bian; Janssen, Dick B

    2015-01-01

    Biocatalytic peptide synthesis will benefit from enzymes that are active at low water levels in organic solvent compositions that allow good substrate and product solubility. To explore the use of proteases from thermophiles for peptide synthesis under such conditions, putative protease genes of the

  15. Comparison of Laboratory Experiments of Chemical, Biological, and Thermal Methods for Treatment of Chlorinated Solvent DNAPL at Kærgård Plantage in Denmark

    DEFF Research Database (Denmark)

    Christophersen, Mette; Christensen, Jørgen Fjeldsø; Jørgensen, Torben H.;

    2010-01-01

    in soil and groundwater, including sulfonamides, barbiturates, aniline, pyridine, chlorinated solvents (chloroethenes), fuel hydrocarbons, mercury, cyanide, lithium and many other compounds.  Wastes were disposed in six pits that continue to leach contaminants to groundwater. Contaminants in groundwater...... are estimated to discharge into the ocean at a rate of 20 m3/year, and public health concerns have prompted the closing of a 1.5 kilometer section of beach at the site. In 2008, the waste pits were excavated down to the water table, and the project is currently focused on evaluation of alternative in situ...... important design objective is to prevent or minimize mobilization of mercury and cyanide.      A series of bench tests have been performed to evaluate the feasibility of treating residual chlorinated solvent dense nonaqueous phase liquid (DNAPL) and other contaminants present in the saturated zone beneath...

  16. HLW partitioning by complex solvent on the basis of chlorinated cobalt dicarbollide, zirconium salt of dibutyl phosphoric acid and polyethylene glycol

    International Nuclear Information System (INIS)

    Addition of chlorinated cobalt dicarbollide to the solvent on the basis of zirconium salt of dibutyl phosphoric acid makes possible to extract not only RE and TPE but also to extract cesium from aqueous nitric acid media. At the same time RE and TPE distribution coefficients noticeably increase because of synergetic effect induced by formation of the complex acid of the possible composition H3[Zr(DBP)4(CCD)3]. The proposed solvent extraction system could be used for partitioning of the main radionuclides contained in high and intermediate level wastes. (author)

  17. Application of in situ chemical oxidation technique with potassium permanganate for the remediation of a shallow aquifer contaminated with chlorinated solvents

    OpenAIRE

    Alaine Santos da Cunha; Reginaldo Antonio Bertolo

    2012-01-01

    In situ chemical oxidation is a method that is frequently being used for the remediation of contaminated areas, since it presents an adequate efficiency in the reduction of the contaminant mass, particularly chlorinated ethenes, in a relatively short period of time. This manuscript presents the results of the application of this method, using the injection of potassium permanganate as the remediation agent, in an impacted area with chlorinated organic compounds, especially 1,1-dichloroethene....

  18. Historical and Retrospective Survey of Monitored Natural Attenuation: A Line of Inquiry Supporting Monitored Natural Attenuation and Enhanced Passive Remediation of Chlorinated Solvents

    International Nuclear Information System (INIS)

    The Department of Energy is sponsoring an initiative to facilitate efficient, effective and responsible use of Monitored Natural Attenuation (MNA) and Enhanced Passive Remediation(EPR) for chlorinated solvents. This Office of Environmental Management Alternative Project, focuses on providing scientific and policy support for MNA/EPR. A broadly representative working group of scientists supports the project along with partnerships with regulatory organizations such as the Interstate Technology Regulatory Council and the Environmental Protection Agency. The initial product of the technical working group was a summary report that articulated the conceptual approach and central scientific tenants of the project, and that identified a prioritized listing of technical targets for field research. This report documented the process in which: (1) scientific ground rules were developed, (2) lines of inquiry were identified and then critically evaluated, (3) promising applied research topics were highlighted in the various lines of inquiry, and (4) these were discussed and prioritized. The summary report will serve as a resource to guide management and decision making throughout the period of the subject MNA/EPR Alternative Project. To support and more fully document the information presented in the summary report, we are publishing a series of supplemental documents that present the full texts from the technical analyses within the various lines of inquiry. The following report - documenting our Historical and Retrospective Survey of Monitored Natural Attenuation - is one of those supplemental documents

  19. Spatial patterns and storage of organic chlorine and chloride in coniferous forest soil in south-east Sweden

    OpenAIRE

    Wesström, Karin

    2002-01-01

    The concentration and storage of organic chlorine and chloride were determined in soil, to a depth of 40 cm, in a coniferous forest in the Stubbetorp catchment area in south-east Sweden. Also, the spatial distribution of the two forms of chlorine was determined. Soil samples were collected at 49 of the nodes in a grid with approximately 105 m between the nodes. The analysis of spatial variability suggested that no spatial autocorrelation was present either within the variable organic chlorine...

  20. A solvent/non-solvent system for achieving solution-processed multilayer organic light-emitting devices

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Yue; Wu, Zhaoxin, E-mail: zhaoxinwu@mail.xjtu.edu.cn; He, Lin; Jiao, Bo; Hou, Xun

    2015-08-31

    We developed a solvent/non-solvent system to fabricate the multilayer organic light-emitting devices (OLEDs) based on poly(N-vinylcarbazole) (PVK) by solution-process. This solvent system consists of both the solvent and non-solvent of PVK, in which fluorescent small molecules could be fully dissolved and directly spin-coated on top of the PVK layer; it could effectively avoid the redissolution of PVK during the spin-coating process of small molecules emitting layer. In the further investigation of this system, we also demonstrated the three-component solvent system, and found out that the third component, a less volatile solvent of PVK, was crucial for preparing a smoother interface between PVK and emitting layer. Compared with OLEDs through the vacuum deposition, the devices fabricated by solution-process from the solvent/non-solvent system showed comparable efficiency, which indicate that the solvent/non-solvent system can be used as an alternative process to prepare the polymer and small molecule multilayer devices through all-solution-process. - Highlights: • We fabricate the multilayer OLEDs by solution-process using a novel system. • We develop a solvent/non-solvent system of polymer (PVK) to avoid redissolution. • Small molecules could be fully dissolved and directly spin-coated on PVK layer. • The devices fabricated by the system and vacuum deposition show comparable efficiency.

  1. A solvent/non-solvent system for achieving solution-processed multilayer organic light-emitting devices

    International Nuclear Information System (INIS)

    We developed a solvent/non-solvent system to fabricate the multilayer organic light-emitting devices (OLEDs) based on poly(N-vinylcarbazole) (PVK) by solution-process. This solvent system consists of both the solvent and non-solvent of PVK, in which fluorescent small molecules could be fully dissolved and directly spin-coated on top of the PVK layer; it could effectively avoid the redissolution of PVK during the spin-coating process of small molecules emitting layer. In the further investigation of this system, we also demonstrated the three-component solvent system, and found out that the third component, a less volatile solvent of PVK, was crucial for preparing a smoother interface between PVK and emitting layer. Compared with OLEDs through the vacuum deposition, the devices fabricated by solution-process from the solvent/non-solvent system showed comparable efficiency, which indicate that the solvent/non-solvent system can be used as an alternative process to prepare the polymer and small molecule multilayer devices through all-solution-process. - Highlights: • We fabricate the multilayer OLEDs by solution-process using a novel system. • We develop a solvent/non-solvent system of polymer (PVK) to avoid redissolution. • Small molecules could be fully dissolved and directly spin-coated on PVK layer. • The devices fabricated by the system and vacuum deposition show comparable efficiency

  2. Efficient organic solar cells processed from hydrocarbon solvents

    Science.gov (United States)

    Zhao, Jingbo; Li, Yunke; Yang, Guofang; Jiang, Kui; Lin, Haoran; Ade, Harald; Ma, Wei; Yan, He

    2016-02-01

    Organic solar cells have desirable properties, including low cost of materials, high-throughput roll-to-roll production, mechanical flexibility and light weight. However, all top-performance devices are at present processed using halogenated solvents, which are environmentally hazardous and would thus require expensive mitigation to contain the hazards. Attempts to process organic solar cells from non-halogenated solvents lead to inferior performance. Overcoming this hurdle, here we present a hydrocarbon-based processing system that is not only more environmentally friendly but also yields cells with power conversion efficiencies of up to 11.7%. Our processing system incorporates the synergistic effects of a hydrocarbon solvent, a novel additive, a suitable choice of polymer side chain, and strong temperature-dependent aggregation of the donor polymer. Our results not only demonstrate a method of producing active layers of organic solar cells in an environmentally friendly way, but also provide important scientific insights that will facilitate further improvement of the morphology and performance of organic solar cells.

  3. Substitution of Organic Solvents in Selected Industrial Cleaning Processes

    DEFF Research Database (Denmark)

    Jacobsen, Thomas; Rasmussen, Pia Brunn

    1997-01-01

    can be replaced with monoesters of fatty acids from vegetable oils (VOFA). The paper describes the selection of other industrial cleaning or degreasing processes where VOC could be replaced by VOFA. Manual degreasing and cleaning processes in metal industry, maintenance and repair of vehicles......Volatile organic solvents (VOC)are becoming increasingly unwanted in industrial processes. Substitution of VOC with non-volatile, low-toxic compounds is a possibility to reduce VOC-use. It has been successfully demonstrated, that organic solvents used in cleaning processes in sheet offset printing......, and industrial coating processes are likely candidates for substitution of VOC with VOFA. Requirements to the resulting surfaces may, however, hinder the replacement. This is especially important when the surface has to be coated in a subsequent step....

  4. Alterations in cognitive and psychological functioning after organic solvent exposure

    Energy Technology Data Exchange (ETDEWEB)

    Morrow, L.A.; Ryan, C.M.; Hodgson, M.J.; Robin, N. (Univ. of Pittsburgh School of Medicine, PA (USA))

    1990-05-01

    Exposure to organic solvents has been linked repeatedly to alterations in both personality and cognitive functioning. To assess the nature and extent of these changes more thoroughly, 32 workers with a history of exposure to mixtures of organic solvents and 32 age- and education-matched blue-collar workers with no history of exposure were assessed with a comprehensive battery of neuropsychological tests. Although both groups were comparable on measures of general intelligence, significant differences were found in virtually all other cognitive domains tested (Learning and Memory, Visuospatial, Attention and Mental Flexibility, Psychomotor Speed). In addition, Minnesota Multiphasic Personality Inventories of exposed workers indicated clinically significant levels of depression, anxiety, somatic concerns and disturbances in thinking. The reported psychological distress was unrelated to degree of cognitive deficit. Finally, several exposure-related variables were associated with poorer performance on tests of memory and visuospatial ability.

  5. A Risk-Based Decision tool to support remediation decision-making for groundwater contaminated with chlorinated solvents

    International Nuclear Information System (INIS)

    Selection of remediation alternatives for large groundwater plumes containing chlorinated solvents are often complex and difficult, in part because they involve competing objectives, e.g. reduction of health risk vs. increased cost. The Department of Energy (DOE) supported development of a Decision Tool to provide a risk-based process for evaluating and comparing remedial options fairly and consistently. The Decision Tool is also intended to provide a process for constructive discussion of alternatives among the appropriate stakeholders. To use the Decision Tool, which is implemented in an Excel spreadsheet, a site manager must evaluate each alternative being considered against six objectives using detailed performance metrics. The impacts of each alternative on the individual objectives are combined through a formal multi-attribute utility analysis. Predetermined or user-specified relative weights for the objectives can be used, and a variety of visual outputs are generated. The usefulness and validity of the Decision Tool was demonstrated through a Pilot Study application for the A-Area Burning Rubble Pits/Miscellaneous Chemical Basin groundwater plume at the DOE Savannah River Site. The Pilot Study results provided a new perspective on the alternatives and objectives by demonstrating: 1) the relatively small public health risks associated with groundwater contamination at this site, 2) that more active approaches had benefits over monitored natural attenuation (MNA) in reducing time required to meet the maximum contaminant level (MCL) and maximizing regulatory responsiveness, 3) that MNA has acceptable public and worker health and safety risks, while enabling a reduction in costs. Use of the Decision Tool also promoted valuable discussion among the various stakeholders, and provided options for sensitivity analyses that can quickly be visualized to assess relative benefits of each of the alternatives. (authors)

  6. Phytoscreening for chlorinated solvents using rapid in vitro SPME sampling: Application to urban plume in Verl, Germany

    Science.gov (United States)

    Limmer, M.A.; Balouet, J.-C.; Karg, F.; Vroblesky, D.A.; Burken, J.G.

    2011-01-01

    Rapid detection and delineation of contaminants in urban settings is critically important in protecting human health. Cores from trees growing above a plume of contaminated groundwater in Verl, Germany, were collected in 1 day, with subsequent analysis and plume mapping completed over several days. Solid-phase microextraction (SPME) analysis was applied to detect tetrachloroethene (PCE) and trichloroethene (TCE) to below nanogram/liter levels in the transpiration stream of the trees. The tree core concentrations showed a clear areal correlation to the distribution of PCE and TCE in the groundwater. Concentrations in tree cores were lower than the underlying groundwater, as anticipated; however, the tree core water retained the PCE:TCE signature of the underlying groundwater in the urban, populated area. The PCE:TCE ratio can indicate areas of differing degradation activity. Therefore, the phytoscreening analysis was capable not only of mapping the spatial distribution of groundwater contamination but also of delineating zones of potentially differing contaminant sources and degradation. The simplicity of tree coring and the ability to collect a large number of samples in a day with minimal disruption or property damage in the urban setting demonstrates that phytoscreening can be a powerful tool for gaining reconnaissance-level information on groundwater contaminated by chlorinated solvents. The use of SPME decreases the detection level considerably and increases the sensitivity of phytoscreening as an assessment, monitoring, and phytoforensic tool. With rapid, inexpensive, and noninvasive methods of detecting and delineating contaminants underlying homes, as in this case, human health can be better protected through screening of broader areas and with far faster response times. ?? 2011 American Chemical Society.

  7. Effect of nitrite on the formation of halonitromethanes during chlorination of organic matter from different origin

    Science.gov (United States)

    Hong, Huachang; Qian, Lingya; Xiao, Zhuoqun; Zhang, Jianqing; Chen, Jianrong; Lin, Hongjun; Yu, Haiying; Shen, Liguo; Liang, Yan

    2015-12-01

    Occurrence of halonitromethanes (HNMs) in drinking water has been a public concern due to the potential risks to human health. Though quite a lot of work has been carried out to understand the formation of HNMs, the relationship between HNMs formation and the nitrite remains unclear. In this study, the effects of nitrite on the formation of HNMs during chlorination of organic matter from different origin were assessed. Organic matter (OM) derived from phoenix tree (fallen leaves: FLOM; green leaves: GLOM) and Microcystis aeruginosa (intracellular organic matter: IOM) were used to mimic the allochthonous and autochthonous organic matter in surface water, respectively. Results showed that HNMs yields were significantly enhanced with the addition of nitrite, and the highest enhancement was observed for FLOM, successively followed by GLOM and IOM, suggesting that the contribution of nitrite to HNMs formation was positively related with SUVA (an indicator for aromaticity) of OM. Therefore, the nitrite contamination should be strictly controlled for the source water dominated by allochthonous OM, which may significantly reduce the formation of HNMs during chlorination. Moreover, given a certain nitrite level, the higher pH resulted in higher stimulation of HNM formation, yet the chlorine dose (always added in excess resulting in residual reactive chlorine), reaction time and temperature did not show obvious influence.

  8. Formation of haloacetamides during chlorination of dissolved organic nitrogen aspartic acid

    Energy Technology Data Exchange (ETDEWEB)

    Chu Wenhai, E-mail: 1world1water@tongji.edu.cn [State Key Laboratory of Pollution Control and Resources Reuse, College of Environmental Science and Engineering, Tongji University, 1239 Siping Road, Shanghai, 200092 (China); Gao Naiyun [State Key Laboratory of Pollution Control and Resources Reuse, College of Environmental Science and Engineering, Tongji University, 1239 Siping Road, Shanghai, 200092 (China); Deng Yang, E-mail: yang.deng@upr.edu [Department of Civil Engineering and Surveying, University of Puerto Rico, P.O. Box 9041, Mayaguez, Puerto Rico, 00681-9041 (Puerto Rico)

    2010-01-15

    The stability of haloacetamides (HAcAms) such as dichloroacetamide (DCAcAm) and trichloroacetamide (TCAcAm) was studied under different experimental conditions. The yield of HAcAms during aspartic acid (Asp) chlorination was measured at different molar ratio of chlorine atom to nitrogen atom (Cl/N), pH and dissolved organic carbon (DOC) mainly consisted of humic acid (HA) mixture. Ascorbic acid showed a better capacity to prevent the decay of DCAcAm and TCAcAm than the other two dechlorinating agents, thiosulfate and sodium sulfite. Lower Cl/N favored the DCAcAm formation, implying that breakpoint chlorination might minimize its generation. The pH decrease could lower the concentration of DCAcAm but favored dichloroacetonitrile (DCAN) formation. DCAcAm yield was sensitive to the DOC due to higher chlorine consumption caused by HA mixture. Two possible pathways of DCAcAm formation during Asp chlorination were proposed. Asp was an important precursor of DCAN, DCAcAm and dichloroacetic acid (DCAA), and thus removal of Asp before disinfection may be a method to prevent the formation of DCAcAm, DCAN and DCAA.

  9. Selective chlorination of natural organic matter: identification of previously unknown disinfection byproducts.

    Science.gov (United States)

    Lavonen, Elin E; Gonsior, Michael; Tranvik, Lars J; Schmitt-Kopplin, Philippe; Köhler, Stephan J

    2013-03-01

    Natural organic matter (NOM) serve as precursors for disinfection byproducts (DBPs) in drinking water production making NOM removal essential in predisinfection treatment processes. We identified molecular formulas of chlorinated DBPs after chlorination and chloramination in four Swedish surface water treatment plants (WTPs) using ultrahigh resolution Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS). Chlorine-containing formulas were detected before and after disinfection and were therefore classified to identify DBPs. In total, 499 DBPs were detected, of which 230 have not been reported earlier. The byproducts had, as a group, significantly lower ratio of hydrogen to carbon (H/C) and significantly higher average carbon oxidation state (COS), double bond equivalents per carbon (DBE/C) and ratio of oxygen to carbon (O/C) compared to Cl-containing components present before disinfection and CHO formulas in samples taken both before and after disinfection. Electrophilic substitution, the proposed most significant reaction pathway for chlorination of NOM, results in carbon oxidation and decreased H/C while O/C and DBE/C is left unchanged. Because the identified DBPs had significantly higher DBE/C and O/C than the CHO formulas we concluded that chlorination of NOM during disinfection is selective toward components with relatively high double bond equivalency and number of oxygen atoms per carbon. Furthermore, choice of disinfectant, dose, and predisinfection treatment at the different WTPs resulted in distinct patterns in the occurrence of DBP formulas.

  10. Personality and long term exposure to organic solvents

    Energy Technology Data Exchange (ETDEWEB)

    Lindstroem, K.; Martelin, T.

    1980-01-01

    Personality, especially emotional reactions of two solvent exposed groups and a nonexposed reference group were described by means of 20 formal, content and check-list type of Rorschach variables. Another objective of the study was to explore the suitability and psychological meaning of other types of Rorschach variables than those applied earlier in the field of behavioral toxicology. The factor analyses grouped the applied variables into factors of Productivity, Ego Strength, Control of Emotionality, Defensive Introversion and Aggressiveness. One solvent group, a patient groups (N.53), was characterized by a high number of Organic signs and a low Genetic Level, indicating possible psychoorganic deterioration. The other solvent group, styrene exposed but subjectively healthy (N.98), was characterized by few emotional reactions, low Anxiety and a low number of Neurotic Signs. the long duration of exposure of the solvent patient group (mean 10.2 +/- 8.7 years) was related to variables of the Productivity factor, a finding that indicates a possible better adjustment of those exposed for a longer time. The duration of exposure of the styrene exposed group (mean 4.9 +/- 3.2 years) revealed a very slight relation to personality variables, but the mean urinary mandelic acid concentration, indicating the level of styrene exposure, correlated with increased emotional reactions. For the most part definite causal conclusions could not be drawn because of the cross-sectional design of the study.

  11. Anaerobic bioremediation of chlorinated solvents in groundwater using edible oil substrate EOS

    Energy Technology Data Exchange (ETDEWEB)

    Sedor, M.; Yoseph, Y. [Remediation Sciences Inc., Newport Beach, CA (United States); Baker, J. [Vironex Inc., Wilmington, DE (United States); Sankey, J. [True Blue Technologies Inc., BC (Canada)

    2007-07-01

    This paper discussed an enhanced anaerobic bioremediation technique that used emulsified edible oils to remediate ground around a dry cleaning establishment in San Jose, California. The project aimed to find a substrate that was easily distributed into the contaminated soils using anaerobic bioremediation. The anaerobic bioremediation process consisted of organic substrates and halorespiring bacteria. Vitamins and trace minerals were used to stimulate Dehalococcoides growth. Soybean oil was used to ferment the hydrogen. Details of the soy and lactate emulsions prepared for the project were provided. Edible oils were used because of their slow-release properties as well as the fact that they are easy to inject and distribute. A barrier technique was also used to define treatment zone dimensions. An in-line metering system was used to dilute the emulsions. Total costs for project were provided. Injection system design options were reviewed. Results of the study demonstrated that the EOS was effectively distributed throughout the treatment area. It was concluded that dramatic improvements in groundwater conditions were observed using the technology. tabs., figs.

  12. On relation of interphase tension in the system of organic solvent-water with parameters of solvent solvation ability

    International Nuclear Information System (INIS)

    It is shown that there is a linear dependence between the empirical parameter, solvent effect (SE), characterizing solvent solvation ability, and interphase tension in the two-phase system organic solvent-water. Analyzing data for 31 solvents, it is established that the largest coefficient of reverse correlation r=-0.98 has been reached when using such an equations as SE=a+b σ/ρ 1/3, where a and b - constants, ρ - solvent density. As far as interphase activity of hyprophobic surfactant decreases linearly with the growth of SE parameter values, then it is follows from the equation found that decrease of interphase tension on the interface water-organic solvent have to lead to decrease of interphase activity of hydrophobic surfactant present in the system

  13. Effects of Chlorination and Heat Treatment on Flour and Gluten Functionality Explored by Solvent Retention Capacity (SRC) and Mixograph

    Science.gov (United States)

    The effects of chlorination and heat treatment on flour and gluten functionality were explored by SRC and mixograph for the soft wheat cultivar, Croplan 594W. Regardless of milling yield, SRC results for chlorinated flour samples showed a decrease in lactic acid SRC values with increasing extent of...

  14. The migration, dissolution, and fate of chlorinated solvents in the urbanized alluvial valleys of the southwestern USA

    Science.gov (United States)

    Jackson, R. E.

    The migration, dissolution, and subsequent fate of spilled chlorinated solvents in the urban alluvial valleys of the southwestern U.S. appear to be governed by a unique set of hydrogeologic and geochemical processes occurring within terrigeneous clastic depositional systems. The alluvial and lacustrine fill of the basins, the trapping of solvents in fine-grained sediments beneath the urbanized valley centers, the oxic conditions typical of the deeper alluvium, and the contaminant-transport patterns produced by large-scale basin pumping combine to produce long aqueous-phase plumes derived from the dissolution of trapped chlorinated solvents. Although of limited aqueous solubility, these dense solvents are sufficiently mobile and soluble in the southwestern alluvial valleys to have produced aqueous plumes that have migrated several kilometers through the deeper alluvium and have contaminated valuable water-supply well fields in California, Arizona, and New Mexico. The typical length of these plumes and the presence of oxic groundwater indicate that it is unlikely that natural attenuation will be a practical remedial option in the southwestern alluvial valleys or in other alluvial systems in which similar hydrogeologic and geochemical conditions exist. Résumé La migration, la dissolution et l'évolution consécutive des rejets de solvants chlorés dans les vallées alluviales du sud-ouest des États-Unis paraissent déterminées par un même ensemble de processus hydrogéologiques et géochimiques intervenant dans des formations de dépôts clastiques terrigènes. Les remplissages alluviaux et lacustres des bassins, le piégeage des solvants par des sédiments fins sous les centres des vallées urbanisées, les conditions oxiques typiques des alluvions plus profondes et les types de transport de contaminants provoqués par le pompage à l'échelle du bassin se combinent pour produire des panaches, étendus dans la phase aqueuse, provenant de la dissolution de

  15. Microcosm Studies to Evaluate Aerobic Cometabolism of Low Concentrations of 1,4-Dioxane by Isobutane-utilizing Microorganisms in the Presence of Chlorinated Solvent Co-contaminants

    Science.gov (United States)

    Rolston, H. M.; Azizian, M.; Hyman, M. R.; Semprini, L.

    2015-12-01

    Due to its use as a stabilizer for chlorinated solvents, 1,4-dioxane (1,4D), a probable human carcinogen, is a common co-contaminant in solvent spills at industrial and military sites and landfills. Its persistence in large groundwater plumes at low concentrations makes it a relevant candidate for in-situ bioremediation via cometabolism. Microcosm studies are being performed to evaluate the capability of aerobic microorganisms to cometabolize mixtures of 1,4D and chlorinated solvents, such as trichloroethylene (TCE), 1,1,1-trichloroethane (1,1,1TCA), and 1,1-dichloroethene (1,1DCE), with isobutane as the primary substrate. Microcosms were constructed using aquifer solids from Fort Carson, Colorado, a site contaminated with 1,4D and TCE, to assess the isobutane uptake and transformation of 1,4D and chlorinated solvents by microorganisms native to the site. Additional microcosms were augmented with Rhodococcus rhodochrous, a bacterium shown to cometabolize 1,4D and chlorinated solvents. Results indicate that native microcosms cometabolized 1,4D upon stimulation with isobutane after a lag period of about 15 days. TCE was also transformed, but at significantly slower rates. The presence of 1,4D and TCE at 500 and 300 ppb, respectively, did not inhibit the growth of native microorganisms on isobutane, with isobutane uptake and 1,4D transformation occurring simultaneously. Bioaugmented microcosms transformed 1,4D immediately after inoculation with R. rhodochrous. Tests in bioaugmented microorganisms indicated that the presence of TCE at low concentrations inhibits but does not block the transformation of 1,4D. Results from the microcosms will be used to design field tests to be performed at Fort Carson. Additional microcosm studies will compare the stimulation of native and bioaugmented microcosms and the transformation of mixtures of 1,4D, 1,1,1TCA and 1,1DCE. Molecular methods will analyze the monoxygenase enzymes expressed in the native and bioaugmented microcosms.

  16. Removal of hexenuronic acid by xylanase to reduce adsorbable organic halides formation in chlorine dioxide bleaching of bagasse pulp.

    Science.gov (United States)

    Nie, Shuangxi; Wang, Shuangfei; Qin, Chengrong; Yao, Shuangquan; Ebonka, Johnbull Friday; Song, Xueping; Li, Kecheng

    2015-11-01

    Xylanase-aided chlorine dioxide bleaching of bagasse pulp was investigated. The pulp was pretreated with xylanase and followed a chlorine dioxide bleaching stage. The ATR-FTIR and XPS were employed to determine the surface chemistry of the control pulp, xylanase treated and chlorine dioxide treated pulps. The hexenuronic acid (HexA) could obviously be reduced after xylanase pretreatment, and the adsorbable organic halides (AOX) were reduced after chlorine dioxide bleaching. Compared to the control pulp, AOX could be reduced by 21.4-26.6% with xylanase treatment. Chlorine dioxide demand could be reduced by 12.5-22% to achieve the same brightness. The ATR-FTIR and XPS results showed that lignin and hemicellulose (mainly HexA) were the main source for AOX formation. Xylanase pretreatment could remove HexA and expose more lignin, which decreased the chlorine dioxide demand and thus reduced formation of AOX. PMID:26263004

  17. 40 CFR Table 3 to Subpart Pppp of... - Default Organic HAP Mass Fraction for Solvents and Solvent Blends

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 12 2010-07-01 2010-07-01 true Default Organic HAP Mass Fraction for Solvents and Solvent Blends 3 Table 3 to Subpart PPPP of Part 63 Protection of Environment ENVIRONMENTAL... of Plastic Parts and Products Pt. 63, Subpt. PPPP, Table 3 Table 3 to Subpart PPPP of Part...

  18. Ozonated water and chlorine effects on the antioxidant properties of organic and conventional broccoli during postharvest

    Directory of Open Access Journals (Sweden)

    Giuseppina Pace Pereira Lima

    2014-04-01

    Full Text Available There is growing interest in studies on sanitizers other than chlorine that can maintain the quality of organic products without affecting their phytochemical content. The effects of using chlorinated and ozonized water treatments, as sanitizing procedures, on the post-harvest quality of organic and conventional broccoli (Brassica oleracea L. cv. Italica was evaluated. The biochemical parameters (chlorophyll, polyphenols, flavonoids, vitamin C and antioxidant capacity of the broccoli samples were analyzed at day 0 (arrival of the plant from the field, original features, and 1, 4 and 7 days after harvest. The polyamine analysis was performed on arrival of the plant from the field and on the first and seventh days. The cultivation procedure influenced polyphenol, vitamin C and total chlorophyll content, and the highest value was observed in organic broccoli after the fourth day. Flavenoid content was higher in organic broccoli. The use of ozone appears not to have had an influence on the amount of polyphenolic, flavonoids and vitamin C during storage. Total chlorophyll content was less affected by ozonized water than by the chlorine treatment as at the first and fourth days of storage. The highest content of putrescine was found in conventional broccoli, while the highest levels of spermidine and spermine were found in organic broccoli. Antioxidant capacity was highest in organic broccoli after day 4 of storage and was affected by the bioactive compounds analyzed. Methods of cultivation influenced natural antioxidant and chlorophyll contents in broccoli under cold storage.

  19. Formation of halogenated organic byproducts during medium-pressure UV and chlorine coexposure of model compounds, NOM and bromide.

    Science.gov (United States)

    Zhao, Quan; Shang, Chii; Zhang, Xiangru; Ding, Guoyu; Yang, Xin

    2011-12-01

    When chlorine is applied before or during UV disinfection of bromide-containing water, interactions between chlorine, bromide and UV light are inevitable. Formation of halogenated organic byproducts was studied during medium-pressure UV (MPUV) and chlorine coexposure of phenol, nitrobenzene and benzoic acid and maleic acid, chosen to represent electron-donating aromatics, electron-withdrawing aromatics, and aliphatic structures in natural organic matter (NOM), respectively. All were evaluated in the presence and absence of bromide. MPUV and chlorine coexposure of phenol produced less total organic halogen (TOX, a collective parameter for halogenated organic byproducts) than chlorination in the dark, and more haloacetic acids instead of halophenols. Increases in TOX were found in the coexposure of nitrobenzene and benzoic acid, but maleic acid was rather inert during coexposure. The presence of bromide increased the formation of brominated TOX but did not significantly affect total TOX formation, in spite of the fact that it reduced hydroxyl radical levels. MPUV and chlorine coexposure of NOM gave a higher differential UV absorbance of NOM and a larger shift to lower molecular weight compounds than chlorination in the dark. However, TOX formation with NOM remained similar to that observed from dark chlorination.

  20. Enzyme catalysis in organic solvents: influence of water content, solvent composition and temperature on Candida rugosa lipase catalyzed transesterification.

    Science.gov (United States)

    Herbst, Daniela; Peper, Stephanie; Niemeyer, Bernd

    2012-12-31

    In the present study the influence of water content, solvent composition and reaction temperature on the transesterification of 1-phenylpropan-2-ol catalyzed by Candida rugosa lipase was examined. Reactions were carried out in different mixtures of hexane and tetrahydrofurane. The studies showed that an increasing water content of the organic solvent results in an increasing enzyme activity and a decreasing enantiomeric excess. Furthermore, a significant influence of the solvent hydrophilicity both on the enzyme activity and on the enantiomeric excess was found. An increase in solvent hydrophilicity leads to a decrease of enzyme activity and an increase of the enantiomeric excess. This indicates that the enzyme becomes more selective with decreasing flexibility. Similar effects were found by variation of the reaction temperature. Taken together, the decrease in conversion and the increase in selectivity with increasing solvent hydrophilicity are induced by the different water contents on the enzyme surface and not by the solvent itself.

  1. Chlorinated pesticides in stream sediments from organic, integrated and conventional farms

    International Nuclear Information System (INIS)

    To determine if current sheep/beef farming practices affect pesticide residues in streams, current-use and legacy chlorinated pesticides were quantified in 100 sediment samples from 15 streams on the South Island of New Zealand. The study involved five blocks of three neighboring farms, with each block containing farms managed by organic, integrated and conventional farming practices. Significantly higher concentrations of dieldrin, ∑ endosulfans, ∑ current-use pesticides, and ∑ chlorinated pesticides were measured in sediments from conventional farms compared to organic and integrated farms. However, streams in the latter two farming categories were not pesticide-free and sometimes contained relatively high concentrations of legacy pesticides. Comparison of measured pesticide concentrations with sediment quality guidelines showed that, regardless of farming practice, mean pesticide concentrations were below the recommended toxicity thresholds. However, up to 23% of individual samples contained chlorpyrifos, endosulfan sulfate, ∑ DDT, dieldrin, or ∑ chlordane concentrations above these thresholds. -- Highlights: •Pesticides were measured in streams in organic, integrated, and conventional farms. •Higher concentrations of some pesticides were found in conventional sites. •Streams in organic and integrated sites were not pesticide free. •Mean pesticide concentrations were below the recommended toxicity thresholds. -- Higher concentrations of several chlorinated pesticides were found in conventional farms; however, organic and integrated practices were not pesticide-free

  2. Treatment of Chlorinated Solvents in Groundwater Beneath an Occupied Building at the Young-Rainey STAR Center, Pinellas, FL

    Energy Technology Data Exchange (ETDEWEB)

    Daniel, Joe [Navarro Research and Engineering; Surovchak, Scott [Dept. of Energy (DOE), Legacy Management; Tabor, Charles [Navarro Research and Engineering

    2016-03-01

    Groundwater contamination, consisting of two dissolved-phase plumes originating from chlorinated solvent source areas, in the southeastern portion of the Young- Rainey Star Center (also known as the Pinellas County, Florida, Site) in Largo, Florida, has migrated beyond the property boundary, beneath the roadways, and beneath adjacent properties to the south and east. Groundwater contamination will persist as long as the onsite contaminant source remains. The origin of the contamination appears to be multiple long-term point sources beneath Building 100, a 4.5 ha (11 acre) building that housed manufacturing facilities during US DOE operations at the site. The site is now owned by Pinellas County, and most of the space inside the building is leased to private companies, so DOE chose not to conduct characterization or remediation through the floor of the building, instead choosing to conduct all work from outside the building. Injection of emulsified soybean oil and a microbial culture has been used at other areas of the site to accelerate naturally occurring bacterial processes that degrade groundwater contaminants to harmless compounds, and that same approach was chosen for this task. The technical approach consisted of installing horizontal wells from outside the building footprint, extending through and around the identified subsurface treatment areas, and terminating beneath the building. Two 107 m (350 ft) long wells, two 122 m (400 ft) long wells, and four 137 m (450 ft) long wells have been installed to intersect the inferred source areas and confirmed contaminant plumes beneath the building. DOE then injected emulsified vegetable oil and a microbial culture into the horizontal wells at each of several target areas beneath the building where the highest groundwater contaminant concentrations have been detected. The target areas are the northwest corner of the building between the old drum storage pad locations and monitoring well PIN12-S35B, the vicinity of

  3. Clostridium hydrogeniformans sp. nov. and Clostridium cavendishii sp. nov., hydrogen-producing bacteria from chlorinated solvent-contaminated groundwater.

    Science.gov (United States)

    Bowman, Kimberly S; Dupré, Rachael E; Rainey, Fred A; Moe, William M

    2010-02-01

    Four hydrogen-producing, aerotolerant, anaerobic bacterial strains isolated from chlorinated solvent-contaminated groundwater were characterized using a polyphasic approach. Three of the strains, designated BL-18, BL-19 and BL-20(T), were found to be identical in 16S rRNA gene sequences and in phenotypic properties. Cells of these strains are Gram-positive-staining, spore-forming, motile rods with peritrichous flagella. Growth occurred at 15-40 degrees C, pH 5.0-10.0 and at NaCl concentrations up to 5 % (w/v). Acid was produced in fermentation of cellobiose, fructose, galactose (weak), glucose, maltose and salicin. Products of fermentation in PYG medium were acetate, butyrate, ethanol, formate, carbon dioxide and hydrogen. Dominant cellular fatty acids when grown in PYG medium were C(13 : 0) iso, C(16 : 0), C(13 : 0) anteiso, C(15 : 0) iso and C(15 : 0) anteiso. The genomic DNA G+C content was 30.4 mol%. These isolates can be differentiated from their closest phylogenetic relative, the cluster I Clostridium species Clostridium frigidicarnis (97.2 % similar to the type strain in 16S rRNA gene sequence), on the basis of phenotypic and chemotaxonomic properties. The other strain characterized in this study, BL-28(T), was Gram-positive-staining with spore-forming, rod-shaped cells. Growth occurred at 15-46 degrees C, pH 6.0-8.5 and at NaCl concentrations up to 3 % (w/v). Acid was produced from cellobiose, dextran, fructose (weak), glucose, maltose, salicin and trehalose. End products of PYG fermentation included acetate, butyrate, pyruvate, carbon dioxide and hydrogen. Dominant cellular fatty acids from cells grown in PYG medium at 30 degrees C were C(14 : 0), C(14 : 0) dimethyl aldehyde, C(16 : 0) and C(12 : 0). The DNA G+C content was 28.5 mol%. Phylogenetic analysis based on 16S rRNA gene sequences revealed that strain BL-28(T) falls within cluster I of the genus Clostridium, but with Clostridium with the names Clostridium hydrogeniformans sp. nov. and Clostridium

  4. Mixed organic solvents induce renal injury in rats.

    Directory of Open Access Journals (Sweden)

    Weisong Qin

    Full Text Available To investigate the injury effects of organic solvents on kidney, an animal model of Sprague-Dawley (SD rats treated with mixed organic solvents via inhalation was generated and characterized. The mixed organic solvents consisted of gasoline, dimethylbenzene and formaldehyde (GDF in the ratio of 2:2:1, and were used at 12,000 PPM to treat the rats twice a day, each for 3 hours. Proteinuria appeared in the rats after exposure for 5-6 weeks. The incidences of proteinuria in male and female rats after exposure for 12 weeks were 43.8% (7/16 and 25% (4/16, respectively. Urinary N-Acetyl-β-(D-Glucosaminidase (NAG activity was increased significantly after exposure for 4 weeks. Histological examination revealed remarkable injuries in the proximal renal tubules, including tubular epithelial cell detachment, cloud swelling and vacuole formation in the proximal tubular cells, as well as proliferation of parietal epithelium and tubular reflux in glomeruli. Ultrastructural examination found that brush border and cytoplasm of tubular epithelial cell were dropped, that tubular epithelial cells were partially disintegrated, and that the mitochondria of tubular epithelial cells were degenerated and lost. In addition to tubular lesions, glomerular damages were also observed, including segmental foot process fusion and loss of foot process covering on glomerular basement membrane (GBM. Immunofluorescence staining indicated that the expression of nephrin and podocin were both decreased after exposure of GDF. In contrast, increased expression of desmin, a marker of podocyte injury, was found in some areas of a glomerulus. TUNEL staining showed that GDF induced apoptosis in tubular cells and glomerular cells. These studies demonstrate that GDF can induce both severe proximal tubular damage and podocyte injury in rats, and the tubular lesions appear earlier than that of glomeruli.

  5. Separation of Phosvitin from Egg Yolk without Using Organic Solvents

    OpenAIRE

    Jung, Samooel; Ahn, Dong Uk; Nam, Ki Chang; Kim, Hyun Joo; Jo, Cheorun

    2013-01-01

    The objective of this study was to develop a new method to separate phosvitin from egg yolk without using organic solvents. Phosvitin was extracted from yolk granules using 10% NaCl or 10% (NH4)2SO4 (final concentration) and then treated with heat to precipitate the lipoproteins from the extracted solution. The optimal pH for the phosvitin extraction from yolk granules was determined, and the iron-binding ability of the extracted phosvitin (final product) was tested. Adding 10% (NH4)2SO4 disr...

  6. [Chlorination byproducts formation potentials of typical nitrogenous organic compounds in water].

    Science.gov (United States)

    Xu, Qian; Xu, Bin; Qin, Cao; Xia, Sheng-Ji; Gao, Nai-Yun; Tian, Fu-Xiang; Li, Da-Peng

    2011-07-01

    Twelve typical nitrogenous organic compounds including herbicides, pesticides, amino acids, industrial products etc in polluted raw water were selected to investigate formation of typical carbonaceous and nitrogenous DBPs during chlorination and chloramination. To indentify the formation mechanism of carbonaceous and nitrogenous disinfection byproducts from nitrogenous chemicals, chlorination and chloroamination of urea herbicides, triazine herbicides, amino acid, and other compounds were investigated. As a result, the potential precursors for different DBPs were defined as well. It has been identified that widely used urea herbicides could produce as many as 9 specific DBPs. The chlorotoluron shows highest reactivity and yields chloroform (CF), monochloroacetic acid (MCAA), dichloroacetic acid (DCAA), 1,1-dichloro-acetone (1,1-DCP), 1,1,1-trichloro-acetone (1,1,1-TCP), chloropicrin (NTCM), dichloro-acetonitrile (DCAN), dimethylnitrosamine (NDMA). The results indicated that aldicarb and dinoseb are important precursors of CF, DCAA, MCAA, NTCM as well. High concentrations of CF and DCAA were found during L-tryptophan chlorination. Furthermore, DBPs formation pathways and mechanisms were suggested during chlorination and chloramination of chlorotoluron, ametryn, dinoseb L-tryptophan.

  7. High exposures to organic solvents among graffiti removers.

    Science.gov (United States)

    Anundi, H; Lind, M L; Friis, L; Itkes, N; Langworth, S; Edling, C

    1993-01-01

    The exposure to organic solvents among 12 graffiti removers was studied. Health effects were also assessed by structured interview and a symptom questionnaire. Blood and urine samples were collected at the end of the day of air sampling. The concentrations of dichloromethane, glycol ethers, trimethylbenzenes and N-methyl-2-pyrrolidinone in the breathing zone of each worker were measured during one working day. The 8-h time-weighted average exposure to dichloromethane ranged from 18 to 1200 mg/m3. The Swedish Permissible Exposure Limit value for dichloromethane is 120 mg/m3. The air concentrations of glycol ethers, trimethylbenzenes and N-methyl-2-pyrrolidinone were low or not detectable. No exposure-related deviations in the serum concentrations of creatinine, aspartate transaminase, alanine transaminase, gamma-glutamyl transpeptidase or hyaluronan or the urine concentrations of alpha 1-microglobulin, beta 2-microglobulin or N-acetyl-beta-glucosaminidase were found. Irritative symptoms of the eyes and upper respiratory tract were more prevalent than in the general population. This study demonstrates that old knowledge about work hazards is not automatically transferred to new professions. Another aspect is that the public is also exposed as the job is performed during daytime in underground stations. At least for short periods, bystanders may be exposed to high concentrations of organic solvent vapours. People with predisposing conditions, e.g. asthmatics, may risk adverse reactions. PMID:8144235

  8. Major neurological disease and occupational exposure to organic solvents.

    Science.gov (United States)

    Seaton, A; Jellinek, E H; Kennedy, P

    1992-09-01

    Five patients are described who presented with major organic brain disease affecting one or more of pyramidal and extrapyramidal tracts, cerebellum, and higher cortical functions. All had a history of 10 years or more of regular occupational exposure to solvents in confined spaces, three in painting inside ships and the others in weapons maintenance and printing. All had been regularly exposed to high air vapour peaks as well as to skin contamination. Four showed some evidence of improvement after the exposure ceased. None was initially suspected of having a toxic encephalopathy by the consultant to whom he was referred. The spectrum of neurological disease presented by these men mirrors closely that described in solvent abusers. All were forced by illness to retire from their work, a circumstance which might have in the past have led to such conditions being missed in cross-sectional studies, which in general have not shown evidence of major disease. We suggest that when such disease occurs nowadays, its cause is usually not suspected. Further epidemiological study of the problem is necessary.

  9. Halogenated volatile organic compounds from the use of chlorine-bleach-containing household products.

    Science.gov (United States)

    Odabasi, Mustafa

    2008-03-01

    Sodium hypochlorite (NaOCl) and many organic chemicals contained in household cleaning products may react to generate halogenated volatile organic compounds (VOCs). Halogenated VOC emissions from eight different chlorine bleach containing household products (pure and diluted) were investigated by headspace experiments. Chloroform and carbon tetrachloride were the leading compounds along with several halogenated compounds in the headspace of chlorine bleach products. One of the most surprising results was the presence of carbon tetrachloride (a probable human carcinogen and a powerful greenhouse gas that was banned for household use by the U.S. Food and Drug Administration) in very high concentrations (up to 101 mg m(-3)). By mixing surfactants or soap with NaOCl, it was shown that the formation of carbon tetrachloride and several other halogenated VOCs is possible. In addition to quantitatively determined halogenated VOCs (n = 15), several nitrogen-containing (n = 4), chlorinated (n = 10), oxygenated compounds (n = 22), and hydrocarbons (n = 14) were identified in the headspace of bleach products. Among these, 1,1-dichlorobutane and 2-chloro-2-nitropropane were the most abundant chlorinated VOCs, whereas trichloronitromethane and hexachloroethane were the most frequently detected ones. Indoor air halogenated VOC concentrations resulting from the use of four selected household products were also measured before, during, and 30 min after bathroom, kitchen, and floor cleaning applications. Chloroform (2.9-24.6 microg m(-3)) and carbon tetrachloride (0.25-459 microg m(-3)) concentrations significantly increased during the use of bleach containing products. During/ before concentration ratios ranged between 8 and 52 (25 +/- 14, average +/- SD) for chloroform and 1-1170 (146 +/- 367, average +/- SD) for carbon tetrachloride, respectively. These results indicated that the bleach use can be important in terms of inhalation exposure to carbon tetrachloride, chloroform and

  10. Peptide synthesis in neat organic solvents with novel thermostable proteases.

    Science.gov (United States)

    Toplak, Ana; Nuijens, Timo; Quaedflieg, Peter J L M; Wu, Bian; Janssen, Dick B

    2015-06-01

    Biocatalytic peptide synthesis will benefit from enzymes that are active at low water levels in organic solvent compositions that allow good substrate and product solubility. To explore the use of proteases from thermophiles for peptide synthesis under such conditions, putative protease genes of the subtilase class were cloned from Thermus aquaticus and Deinococcus geothermalis and expressed in Escherichia coli. The purified enzymes were highly thermostable and catalyzed efficient peptide bond synthesis at 80°C and 60°C in neat acetonitrile with excellent conversion (>90%). The enzymes tolerated high levels of N,N-dimethylformamide (DMF) as a cosolvent (40-50% v/v), which improved substrate solubility and gave good conversion in 5+3 peptide condensation reactions. The results suggest that proteases from thermophiles can be used for peptide synthesis under harsh reaction conditions.

  11. Development and in situ implementation of a chemical process for reductive dechlorination of chlorinated solvents in polluted aquifers

    OpenAIRE

    Betelu, Stéphanie; Rodrigues, Romain; Noel, Cécile; Colombano, Stéfan; Simon, Apolline; Epardeau, Patrick; Marion, Roland; Ignatiadis, Ioannis

    2015-01-01

    International audience Reductive dechlorination (RDC), using strong reducers, is one of the most important emerging remediation techniques for chlorinated hydrocarbons (CHC). RDC by Nanosized Zero Valent Iron (NZVI) is a powerful electrochemical redox system that has shown promising experimental results for the development of remediation technologies to treat contaminated sites [1, 2]. Although NZVI has excellent characteristics as environmental reactant, its application to the contaminate...

  12. The cellular uptake of meta-tetra(hydroxyphenyl)chlorin entrapped in organically modified silica nanoparticles is mediated by serum proteins

    International Nuclear Information System (INIS)

    Nanosized objects made of various materials are gaining increasing attention as promising vehicles for the delivery of therapeutic and diagnostic agents for cancer. Photodynamic therapy (PDT) appears to offer a very attractive opportunity to implement drug delivery systems since no release of the sensitizer is needed to obtain the therapeutic effect and the design of the nanovehicle should be much easier. The aim of our study was to investigate the use of organic-modified silica nanoparticles (NPs) for the delivery of the second-generation photosensitizer meta-tetra(hydroxyphenyl)chlorin (mTHPC) to cancer cells in vitro. mTHPC was entrapped in NPs (∼33 nm diameter) in a monomeric form which produced singlet oxygen with a high efficiency. In aqueous media with high salt concentrations, the NPs underwent aggregation and precipitation but their stability could be preserved in the presence of foetal bovine serum. The cellular uptake, localization and phototoxic activity of mTHPC was determined comparatively in human oesophageal cancer cells after its delivery by the NPs and the standard solvent ethanol/poly(ethylene glycol) 400/water (20:30:50, by vol). The NP formulation reduced the cellular uptake of mTHPC by about 50% in comparison to standard solvent while it did not affect the concentration-dependent photokilling activity of mTHPC and its intracellular localization. Fluorescence resonance energy transfer measurements, using NPs with mTHPC physically entrapped and a cyanine covalently linked, and ultracentrifugation experiments indicated that mTHPC is transferred from NPs to serum proteins when present in the medium. However, the coating of the NP surface with poly(ethylene glycol) largely prevented the transfer to proteins. In conclusion, mTHPC is rapidly transferred from the uncoated nanoparticles to the serum proteins and then internalized by the cells as a protein complex, irrespective of its modality of delivery.

  13. The cellular uptake of meta-tetra(hydroxyphenyl)chlorin entrapped in organically modified silica nanoparticles is mediated by serum proteins

    Energy Technology Data Exchange (ETDEWEB)

    Compagnin, Chiara; Mognato, Maddalena; Celotti, Lucia; Moret, Francesca; Fede, Caterina; Selvestrel, Francesco; Echevarria, Iria M Rio; Reddi, Elena [Department of Biology, University of Padova, via Ugo Bassi 58/B, I-35131 Padova (Italy); Bau, Luca; Arduini, Maria; Mancin, Fabrizio [Department of Chemical Sciences, University of Padova, via Marzolo 1, I-35131 Padova (Italy); Miotto, Giovanni, E-mail: elena.reddi@unipd.i [Department of Biological Chemistry, University of Padova, via Ugo Bassi 58/B, I-35131 Padova (Italy)

    2009-08-26

    Nanosized objects made of various materials are gaining increasing attention as promising vehicles for the delivery of therapeutic and diagnostic agents for cancer. Photodynamic therapy (PDT) appears to offer a very attractive opportunity to implement drug delivery systems since no release of the sensitizer is needed to obtain the therapeutic effect and the design of the nanovehicle should be much easier. The aim of our study was to investigate the use of organic-modified silica nanoparticles (NPs) for the delivery of the second-generation photosensitizer meta-tetra(hydroxyphenyl)chlorin (mTHPC) to cancer cells in vitro. mTHPC was entrapped in NPs ({approx}33 nm diameter) in a monomeric form which produced singlet oxygen with a high efficiency. In aqueous media with high salt concentrations, the NPs underwent aggregation and precipitation but their stability could be preserved in the presence of foetal bovine serum. The cellular uptake, localization and phototoxic activity of mTHPC was determined comparatively in human oesophageal cancer cells after its delivery by the NPs and the standard solvent ethanol/poly(ethylene glycol) 400/water (20:30:50, by vol). The NP formulation reduced the cellular uptake of mTHPC by about 50% in comparison to standard solvent while it did not affect the concentration-dependent photokilling activity of mTHPC and its intracellular localization. Fluorescence resonance energy transfer measurements, using NPs with mTHPC physically entrapped and a cyanine covalently linked, and ultracentrifugation experiments indicated that mTHPC is transferred from NPs to serum proteins when present in the medium. However, the coating of the NP surface with poly(ethylene glycol) largely prevented the transfer to proteins. In conclusion, mTHPC is rapidly transferred from the uncoated nanoparticles to the serum proteins and then internalized by the cells as a protein complex, irrespective of its modality of delivery.

  14. Regioselective self-acylating cyclodextrins in organic solvent

    Science.gov (United States)

    Cho, Eunae; Yun, Deokgyu; Jeong, Daham; Im, Jieun; Kim, Hyunki; Dindulkar, Someshwar D.; Choi, Youngjin; Jung, Seunho

    2016-03-01

    Amphiphilic cyclodextrins have been synthesized with self-acylating reaction using vinyl esters in dimethylformamide. In the present study no base, catalyst, or enzyme was used, and the structural analyses using thin layer chromatography, nuclear magnetic resonance spectroscopy and mass spectrometry show that the cyclodextrin is substituted preferentially by one acyl moiety at the C2 position of the glucose unit, suggesting that cyclodextrin functions as a regioselective catalytic carbohydrate in organic solvent. In the self-acylation, the most acidic OH group at the 2-position and the inclusion complexing ability of cyclodextrin were considered to be significant. The substrate preference was also observed in favor of the long-chain acyl group, which could be attributed to the inclusion ability of cyclodextrin cavity. Furthermore, using the model amphiphilic building block, 2-O-mono-lauryl β-cyclodextrin, the self-organized supramolecular architecture with nano-vesicular morphology in water was investigated by fluorescence spectroscopy, dynamic light scattering and transmission electron microscopy. The cavity-type nano-assembled vesicle and the novel synthetic methods for the preparation of mono-acylated cyclodextrin should be of great interest with regard to drug/gene delivery systems, functional surfactants, and carbohydrate derivatization methods.

  15. Relevance of an organic solvent for absorption of siloxanes.

    Science.gov (United States)

    Ghorbel, Leila; Tatin, Romuald; Couvert, Annabelle

    2014-01-01

    A wide range of siloxanes exist but the most abundant in biogas are Hexamethyldisiloxane (L2) and Octamethyltrisiloxane (L3) as linear siloxanes and Octamethylcyclotetrasiloxane (D4) as a cyclic siloxane. In order to remove volatile organic compound from biogas, different processes can be used. A promising process for siloxane removal is their absorption in an organic solvent. In this work, three oils were tested to absorb the selected siloxanes: silicone oil 47V20, Seriola 1510 and Polyalphaolefin. Initially, the characterization of these oils was realized by measuring their viscosities and densities, depending on temperature. The second time, the absorption capacity of the siloxanes by selected oils was characterized through the determination of their Henry's constants, but also owing to the implementation of a wet-wall column. Both Henry's constants and removal efficiencies in continuous regime revealed that silicone oil (47V20) can be considered as the most efficient oil among the three selected siloxanes. Moreover, the cyclic siloxane (D4) showed more affinity with oils than linear siloxanes. Silicone oil 47V20 appeared to be the best oil (intermediate price 14 euro/L, low viscosity, low volatility, chemical inertness (no corrosion) and resistance to high and low temperatures). PMID:24600877

  16. Rapid dechlorination of chlorinated organic compounds by nickel/iron bimetallic system in water

    Institute of Scientific and Technical Information of China (English)

    TONG Shao-ping; WEI Hong; MA Chun-an; LIU Wei-ping

    2005-01-01

    Detoxification of chlorinated organic compounds via reaction with nickel/iron powder was implemented in aqueous solution. Compared to iron, nickel/iron bimetallic powder had higher hydrodechlorination activities for both atrazine (ATR) and p-chlorophenol (pCP); nickel/iron (2.96%, w/w) was shown to have the largest specific surface area and the optimum proportion for the dechlorination of both ATR and pCP. Electrochemical measurements showed that the adsorbed hydrogen atom on the nickel must have been the dominant reductive agent for the dechlorination of both ATR andpCP in this system.

  17. Enzymatic Synthesis of Esculin Ester in Ionic Liquids Buffered with Organic Solvents

    DEFF Research Database (Denmark)

    Hu, Yifan; Guo, Zheng; Lue, Bena-Marie;

    2009-01-01

    The enzymatic esterification of esculin catalyzed by Candida antarctica lipase B (Novozym 435) was carried out in ionic liquid (IL)-organic solvent mixed systems in comparison with individual systems. The reaction behaviors in IL-organic solvents were systemically evaluated using acetone as a model...... solvent. With organic solvents as media, the esterification rates of esculin depended mainly on its solubility in solvents; for the reactions in ILs, the reaction rates were generally low, and the anion part of the IL played a critical role in enzyme activity. Therefore, the esterification of esculin......](-) > [MDEGSO(4)](-) > [OctSO(4)](-) > [ES](-) = [DMP](-) = [OTs](-) = CI-. The reaction behaviors differed in different systems and largely depended on the properties of the ILs and organic solvents. In general, improvements were observed in terms of both solubility and reaction efficiency. The knowledge...

  18. Solvents in Organic Synthesis: Replacement and Multi-step Reaction Systems

    DEFF Research Database (Denmark)

    Gani, Rafiqul; Gómez, Paola Arenas; Folic, Milica;

    2008-01-01

    with the principles of green chemistry, highlight the need to minimize and optimize the use of organic solvents as much as possible. One important step in optimizing organic solvent use is the identification of suitable ‘greener' solvents that can help to minimize the environmental, health and safety concerns during...... design and commercial manufacture of chemical products. A method for selecting appropriate ‘greener' solvents for the promotion of a class of organic reactions has been previously developed by Gani et al. This method employs estimates of thermodynamic properties to generate a knowledge base of reaction...

  19. USE OF FIELD-DEPLOYED GAS CHROMATOGRAPH AND MEMBRANE INTERPHASE PROBE (MIP) TECHNOLOGY TO AID IN THE CHARACTERIZATION OF CHLORINATED SOLVENTS IN SOIL AT THE PEACH ORCHARD ROAD SITE, AUGUSTA, GA

    Science.gov (United States)

    This study used a field-deployed gas chromatograph and a direct-push membrane interface probe (MIP) to give real-time characterization of the chlorinated-solvent content of soil at various depths. Soil was screened at one-foot intervals from one to 62 feet below land surface at a...

  20. Epidemiology of organic solvents and connective tissue disease

    OpenAIRE

    Garabrant, David H.; Dumas, Constantine

    1999-01-01

    Case reports suggest that solvents are associated with various connective tissue diseases (systemic sclerosis, scleroderma, undifferentiated connective tissue disease, systemic lupus erythematosis, and rheumatoid arthritis), particularly systemic sclerosis. A small number of epidemiological studies have shown statistically significant but weak associations between solvent exposure, systemic sclerosis, and undifferentiated connective tissue disease. However, the interpretation of these positiv...

  1. Modeling structure and flexibility of Candida antarctica lipase B in organic solvents

    Directory of Open Access Journals (Sweden)

    Pleiss Jürgen

    2008-02-01

    Full Text Available Abstract Background The structure and flexibility of Candida antarctica lipase B in water and five different organic solvent models was investigated using multiple molecular dynamics simulations to describe the effect of solvents on structure and dynamics. Interactions of the solvents with the protein and the distribution of water molecules at the protein surface were examined. Results The simulated structure was independent of the solvent, and had a low deviation from the crystal structure. However, the hydrophilic surface of CALB in non-polar solvents decreased by 10% in comparison to water, while the hydrophobic surface is slightly increased by 1%. There is a large influence on the flexibility depending on the dielectric constant of the solvent, with a high flexibility in water and a low flexibility in organic solvents. With decreasing dielectric constant, the number of surface bound water molecules significantly increased and a spanning water network with an increasing size was formed. Conclusion The reduced flexibility of Candida antarctica lipase B in organic solvents is caused by a spanning water network resulting from less mobile and slowly exchanging water molecules at the protein-surface. The reduced flexibility of Candida antarctica lipase B in organic solvent is not only caused by the interactions between solvent-protein, but mainly by the formation of a spanning water network.

  2. Predicting total organic halide formation from drinking water chlorination using quantitative structure-property relationships.

    Science.gov (United States)

    Luilo, G B; Cabaniss, S E

    2011-10-01

    Chlorinating water which contains dissolved organic matter (DOM) produces disinfection byproducts, the majority of unknown structure. Hence, the total organic halide (TOX) measurement is used as a surrogate for toxic disinfection byproducts. This work derives a robust quantitative structure-property relationship (QSPR) for predicting the TOX formation potential of model compounds. Literature data for 49 compounds were used to train the QSPR in moles of chlorine per mole of compound (Cp) (mol-Cl/mol-Cp). The resulting QSPR has four descriptors, calibration [Formula: see text] of 0.72 and standard deviation of estimation of 0.43 mol-Cl/mol-Cp. Internal and external validation indicate that the QSPR has good predictive power and low bias (‰<‰1%). Applying this QSPR to predict TOX formation by DOM surrogates - tannic acid, two model fulvic acids and two agent-based model assemblages - gave a predicted TOX range of 136-184 µg-Cl/mg-C, consistent with experimental data for DOM, which ranged from 78 to 192 µg-Cl/mg-C. However, the limited structural variation in the training data may limit QSPR applicability; studies of more sulfur-containing compounds, heterocyclic compounds and high molecular weight compounds could lead to a more widely applicable QSPR.

  3. Natural solar photolysis of total organic chlorine, bromine and iodine in water.

    Science.gov (United States)

    Abusallout, Ibrahim; Hua, Guanghui

    2016-04-01

    Municipal wastewater has been increasingly used to augment drinking water supplies due to the growing water scarcity. Wastewater-derived disinfection byproducts (DBPs) may negatively affect the aquatic ecosystems and human health of downstream communities during water reuse. The objective of this research was to determine the degradation kinetics of total organic chlorine (TOCl), bromine (TOBr) and iodine (TOI) in water by natural sunlight irradiation. Outdoor solar photolysis experiments were performed to investigate photolytic degradation of the total organic halogen (TOX) formed by fulvic acid and real water and wastewater samples. The results showed that TOX degradation by sunlight irradiation followed the first-order kinetics with half-lives in the range of 2.6-10.7 h for different TOX compounds produced by fulvic acid. The TOX degradation rates were generally in the order of TOI > TOBr ≅ TOCl(NH2Cl) > TOCl(Cl2). High molecular weight TOX was more susceptible to solar photolysis than corresponding low molecular weight halogenated compounds. The nitrate and sulfite induced indirect TOX photolysis rates were less than 50% of the direct photolysis rates under the conditions of this study. Fulvic acid and turbidity in water reduced TOX photodegradation. These results contribute to a better understanding of the fate of chlorinated, brominated and iodinated DBPs in surface waters.

  4. Adverse effects of organic solvents on fertility and reproduction ; a critical review

    NARCIS (Netherlands)

    Koëter, H.B.W.M.; Blijleven, W.G.H.; Dreef-van der Meulen, H.C.; Stijkel, A.; Zielhuis, R.L.

    1989-01-01

    From this literature survey it appeared that there is a considerable lack of information with respect to organic solvents both of human and laboratory animal fertility and reproduction: only xylene is reasonable studied in animals. Since human exposures to a number of organic solvents is widespread

  5. Immobilization of Lipase by Adsorption Onto Magnetic Nanoparticles in Organic Solvents.

    Science.gov (United States)

    Shi, Ying; Liu, Wei; Tao, Qing-Lan; Jiang, Xiao-Ping; Liu, Cai-Hong; Zeng, Sha; Zhang, Ye-Wang

    2016-01-01

    In order to improve the performance of lipase in organic solvents, a simple immobilization method was developed by adsorption of lipase onto Fe₃O₄@ SiO₂magnetic nanoparticles in organic solvent. Among the solvents tested, toluene was found to be the most effective solvent for the immobilization. A maximum immobilization yield of 97% and relative activity of 124% were achieved in toluene at 30 °C. The optimal temperature, enzyme loading and water activity were 30 °C, 1.25 mg/mg support and 0.48 aw, respectively. The residual activity of immobilized lipase was 67% after 10 cycles of use. The advantages of the immobilized lipase including easy recovery, high stability, and enhanced activity of immobilized lipase in organic solvents show potential industrial applications in anhydrous solvents. PMID:27398494

  6. Correlation of low volatile organic chlorine (LVOCI) and PCDD/Fs in verious municipal waste incinerators (MWI)

    Energy Technology Data Exchange (ETDEWEB)

    Watanabe, N.; Minami, Y.; Mizutani, S.; Takatsuki, H. [Kyoto University Environment Preservation Center, Kyoto (Japan); Takakura, A. [Osaka City Institute of Public Health and Environmental Sciences, Osaka (Japan)

    2004-09-15

    Formation of PCDD/Fs through combustion has been a matter of concern for a few decades. As research on the formation mechanism has advanced, it has been revealed that PCDD/Fs are only a limited fraction of the various organic chlorinated compounds. For this reason, the group parameter of ''organic halogens'' is considered to be a good indicator or surrogate for PCDD/Fs. However, the traditional method of halogen determination using combustion - coulometric titration is neither selective nor sensitive to the elements. This problem was overcome by the development of atomic emission spectrometry (AES) detection of halogens using radiofrequency helium plasma. This method was initially introduced by Rice et al in 1985 as a GC detector and improved by others. We have modified the plasma to barrier discharge and simplified the optical detection. Gaseous organic chlorine was determined by adsorptive collection and direct introduction of thermally desorbed sample to the plasma. In order to examine the correlation of organic chlorine and PCDD/Fs, we have measured organic chlorine in conjunction with the legislated periodical PCDD/Fs inspections of MWI stack gas emissions in Osaka City, Japan. From data collected during 2001, a fairly good correlation between low-volatile organic chlorine (LVOCl) and PCDD/Fs was found, while semi-volatile organic chlorine (SVOCl) gave a poor correlation with PCDD/Fs. However, a study conducted in 2002 resulted in some shift of the regression line of LVOCl - PCDD/Fs. As the determination of LVOCl involves fractionation based on boiling points (b.p.), it is expected that removal of PCDD/Fs with adsorptive devices influences the regression. In this paper, the experimental results are summarized and the effect of the gas treatment condition on the correlation between LVOCl and PCDD/Fs is discussed.

  7. FT-IR spectroscopy and DFT calculation study on the solvent effects of benzaldehyde in organic solvents.

    Science.gov (United States)

    Li, Yi; Zhang, Hui; Liu, Qing

    2012-02-01

    FT-IR spectra of benzaldehyde in 11 different organic solvents were recorded and analyzed. The density functional theory (DFT) B3LYP/6-31G* method was chosen to calculate the infrared spectrum of benzaldehyde in gaseous state. The electrostatic effects of different solvents in benzaldehyde solutions were calculated using DFT with the self-consistent isodensity polarizable continuum model (SCI-PCM). Two remarkable carbonyl (C=O) peaks of benzaldehyde were observed by FT-IR in alcohol solvents, which were caused by different hydrogen bond species and explained by ab initio calculation. The results showed that the combination of SCI-PCM model and ab initio calculation could give excellent agreements with FT-IR spectra of title compound in solutions.

  8. Solvents, Ethanol, Car Crashes and Tolerance: How Risky is Inhalation of Organic Solvents?

    Science.gov (United States)

    A research program in the National Health and Environmental Effects Research Laboratory of the U.S. EPA has led to some surprising considerations regarding the potential hazard of exposure to low concentrations of solvent vapors. This program involved conducting experiments to ch...

  9. Exposure Characteristics of Construction Painters to Organic Solvents

    Science.gov (United States)

    Park, Hyunhee; Park, Hae Dong; Jang, Jae-Kil

    2015-01-01

    Background Construction painters have not been studied well in terms of their hazards exposure. The objective of this study was to evaluate the exposure levels of total volatile organic compounds (TVOCs) for painters in the construction industry. Methods Activity-specific personal air samplings were carried out in three waterproofing activities [polyurethane (PU), asphalt, and cement mortar] and three painting activities (epoxy, oil based, and water based) by using organic-vapor-monitor passive-sampling devices. Gas chromatograph with flame ionization detector could be used for identifying and quantifying individual organic chemicals. The levels of TVOCs, by summing up 15 targeted substances, were expressed in exposure-index (EI) values. Results As arithmetic means in the order of concentration levels, the EIs of TVOCs in waterproofing works were 10.77, 2.42, 1.78, 1.68, 0.47, 0.07, and none detected (ND) for indoor PU-primer task, outdoor PU-primer task, outdoor PU-resin task, indoor PU-resin task, asphalt-primer task, asphalt-adhesive task, and cement-mortar task, respectively. The highest EI for painting works was 5.61 for indoor epoxy-primer task, followed by indoor epoxy-resin task (2.03), outdoor oil-based-spray-paint task (1.65), outdoor water-based-paint task (0.66), and indoor oil-based-paint task (0.15). Assuming that the operations were carried out continuously for 8 hours without breaks and by using the arithmetic means of EIs for each of the 12 tasks in this study, 58.3% (7 out of 12) exceeded the exposure limit of 100% (EI > 1.0), while 8.3% (1 out of 12) was in 50–100% of exposure limit (0.5 > EI > 1.0), and 4 tasks out of 12 were located in less than 50% of the limit range (EI exposed to various solvents, including carcinogens and reproductive toxins, and the levels of TVOC concentration in many of the painting tasks exceeded the exposure limits. Construction workers need to be protected from chemical agents during their painting works by

  10. Dichloroacetonitrile and dichloroacetamide can form independently during chlorination and chloramination of drinking waters, model organic matters, and wastewater effluents.

    Science.gov (United States)

    Huang, Huang; Wu, Qian-Yuan; Hu, Hong-Ying; Mitch, William A

    2012-10-01

    The increasing usage of organic nitrogen-rich wastewater- or algal-impacted waters, and chloramines for secondary disinfection, raises concerns regarding the formation of haloacetonitriles, haloacetamides and other nitrogenous disinfection byproducts (N-DBPs). Previous research obtained contradictory results regarding the relative importance of chlorination or chloramination for promoting these byproducts, but applied chlorine and chloramines at different doses and exposure periods. Additionally, mechanistic work, mostly using model precursors, suggested that haloacetonitrile and haloacetamide formation should be correlated because hydrolysis of haloacetonitriles forms haloacetamides. In this work, the formation of dichloroacetonitrile (DCAN) and dichloroacetamide (DCAcAm) were compared across a range of chlorine and chloramine exposures for drinking waters, wastewater effluents, algal extracellular polymeric substances (EPS), NOM isolates and model precursors. While chlorination favored formation of DCAN over DCAcAm, chloramination nearly always formed more DCAcAm than DCAN, suggesting the existence of haloacetamide formation pathways that are independent of the hydrolysis of haloacetonitriles. Experiments with asparagine as a model precursor also suggested DCAcAm formation without a DCAN intermediate. Application of (15)N-labeled monochloramine indicated initial rapid formation of both DCAN and DCAcAm by pathways where the nitrogen originated from organic nitrogen precursors. However, slower formation occurred by pathways involving chloramine incorporation into organic precursors. While wastewater effluents and algal EPS tended to be more potent precursors for DCAN during chlorination, humic materials were more potent precursors for DCAcAm during chlorination and for both DCAN and DCAcAm during chloramination. These results suggest that, rather than considering haloacetamides as haloacetonitrile hydrolysis products, they should be treated as a separate N

  11. High-Pressure Solvent Vapor Annealing with a Benign Solvent To Rapidly Enhance the Performance of Organic Photovoltaics.

    Science.gov (United States)

    Jung, Buyoung; Kim, Kangmin; Eom, Yoomin; Kim, Woochul

    2015-06-24

    A high-pressure solvent vapor annealing (HPSVA) treatment is suggested as an annealing process to rapidly achieve high-performance organic photovoltaics (OPVs); this process can be compatible with roll-to-roll processing methods and uses a benign solvent: acetone. Solvent vapor annealing can produce an advantageous vertical distribution in the active layer; however, conventional solvent vapor annealing is also time-consuming. To shorten the annealing time, high-pressure solvent vapor is exposed on the active layer of OPVs. Acetone is a nonsolvent for poly(3-hexylthiophene-2,5-diyl) (P3HT), but it can dissolve small amounts of 1-(3-methoxycarbonyl)-propyl-1,1-phenyl-(6,6)C61 (PCBM). Acetone vapor molecules can penetrate into the active layer under high vapor pressure conditions to alter the morphology. HPSVA induces a PCBM-rich phase near the cathode and facilitates the transport of free charge carriers to the electrode. Although P3HT is not soluble in acetone, locally rearranged P3HT crystallites are generated. The performance of OPV films was enhanced after HPSVA; the film treated at 30 kPa for 10 s showed optimum performance. Additionally, this HPSVA method could be adapted for mass production because the temporary exposure of films to high-pressure acetone vapor in ambient conditions also improved performance.

  12. Impairment of colour vision in workers exposed to organic solvents

    OpenAIRE

    Semple, S.; Dick, F.; Osborne, A.; Cherrie, J; Soutar, A; Seaton, A.; Haites, N.

    2000-01-01

    OBJECTIVES—To investigate loss of colour vision related to exposure to solvents and the role of three enzyme polymorphisms in modifying the risk in exposed workers.
METHODS—A sample was studied of 68 male dockyard workers and 42 male community controls with and without neuropsychological symptoms from a previous cross sectional study. Indices of cumulative and intensity based exposure to solvents were calculated for all subjects. Alcohol, drug, and smoking histories were obtained. Colour visi...

  13. Fast molecular beacon hybridization in organic solvents with improved target specificity.

    Science.gov (United States)

    Dave, Neeshma; Liu, Juewen

    2010-12-01

    DNA hybridization is of tremendous importance in biology, bionanotechnology, and biophysics. Molecular beacons are engineered DNA hairpins with a fluorophore and a quencher labeled on each of the two ends. A target DNA can open the hairpin to give an increased fluorescence signal. To date, the majority of molecular beacon detections have been performed only in aqueous buffers. We describe herein DNA detection in nine different organic solvents, methanol, ethanol, isopropanol, acetonitrile, formamide, dimethylformamide (DMF), dimethyl sulfoxide (DMSO), ethylene glycol, and glycerol, varying each up to 75% (v/v). In comparison with detection in water, the detection in organic solvents showed several important features. First, the molecular beacon hybridizes to its target DNA in the presence of all nine solvents up to a certain percentage. Second, the rate of this hybridization was significantly faster in most organic solvents compared with water. For example, in 56% ethanol, the beacon showed a 70-fold rate enhancement. Third, the ability of the molecular beacon to discriminate single-base mismatch is still maintained. Lastly, the DNA melting temperature in the organic solvents showed a solvent concentration-dependent decrease. This study suggests that molecular beacons can be used for applications where organic solvents must be involved or organic solvents can be intentionally added to improve the molecular beacon performance.

  14. Water-enhanced solubility of carboxylic acids in organic solvents and its applications to extraction processes

    Energy Technology Data Exchange (ETDEWEB)

    Starr, J.N.; King, C.J.

    1991-11-01

    The solubilities of carboxylic acids in certain organic solvents increase remarkably with an increasing amount of water in the organic phase. This phenomenon leads to a novel extract regeneration process in which the co-extracted water is selectively removed from an extract, and the carboxylic acid precipitates. This approach is potentially advantageous compared to other regeneration processes because it removes a minor component of the extract in order to achieve a large recovery of acid from the extract. Carboxylic acids of interest include adipic acid, fumaric acid, and succinic acid because of their low to moderate solubilities in organic solvents. Solvents were screened for an increase in acid solubility with increased water concentration in the organic phase. Most Lewis-base solvents were found to exhibit this increased solubility phenomena. Solvents that have a carbonyl functional group showed a very large increase in acid solubility. 71 refs., 52 figs., 38 tabs.

  15. Impact of bromide on halogen incorporation into organic moieties in chlorinated drinking water treatment and distribution systems.

    Science.gov (United States)

    Tan, J; Allard, S; Gruchlik, Y; McDonald, S; Joll, C A; Heitz, A

    2016-01-15

    The impact of elevated bromide concentrations (399 to 750 μg/L) on the formation of halogenated disinfection by-products (DBPs), namely trihalomethanes, haloacetic acids, haloacetonitriles, and adsorbable organic halogen (AOX), in two drinking water systems was investigated. Bromine was the main halogen incorporated into all of the DBP classes and into organic carbon, even though chlorine was present in large excess to maintain a disinfectant residual. Due to the higher reactivity of bromine compared to chlorine, brominated DBPs were rapidly formed, followed by a slower increase in chlorinated DBPs. Higher bromine substitution and incorporation factors for individual DBP classes were observed for the chlorinated water from the groundwater source (lower concentration of dissolved organic carbon (DOC)), which contained a higher concentration of bromide, than for the surface water source (higher DOC). The molar distribution of adsorbable organic bromine to chlorine (AOBr/AOCl) for AOX in the groundwater distribution system was 1.5:1 and almost 1:1 for the surface water system. The measured (regulated) DBPs only accounted for 16 to 33% of the total organic halogen, demonstrating that AOX measurements are essential to provide a full understanding of the formation of halogenated DBPs in drinking waters. In addition, the study demonstrated that a significant proportion (up to 94%) of the bromide in source waters can be converted AOBr. An evaluation of AOBr and AOCl through a second groundwater treatment plant that uses conventional treatment processes for DOC removal produced 70% of AOX as AOBr, with 69% of the initial source water bromide converted to AOBr. Exposure to organobromine compounds is suspected to result in greater adverse health consequences than their chlorinated analogues. Therefore, this study highlights the need for improved methods to selectively reduce the bromide content in source waters.

  16. The elimination of chlorinated, chlorofluorocarbon, and other RCRA hazardous solvents from the Y-12 Plant's enriched uranium operations

    International Nuclear Information System (INIS)

    A major driving force in waste minimization within the plant is the reduction of mixed radioactive wastes associated with operations on highly enriched uranium. High enriched uranium has a high concentration of the uranium-235 isotope (up to 97.5% enrichment) and is radioactive, giving off alpha and low level gamma radiation. The material is fissionable with as little as two pounds dissolved in water being capable of producing a spontaneous chain reaction. For these reasons the material is processed in small batches or small geometries. Additionally, the material is completely recycled because of its strategic and monetary value. Since the early eighties, the plant has had an active waste minimization program which has concentrated on substitution of less hazardous solvents wherever possible. The following paper summarizes efforts in two areas - development of a water-based machining coolant to replace perchloroethylene and substitution of an aliphatic solvent to replace solvents producing hazardous wastes as defined by the Resource, Conservation, and Recovery Act (RCRA)

  17. Effects of organic solvents on the barrier properties of human nail.

    Science.gov (United States)

    Smith, Kelly A; Hao, Jinsong; Li, S Kevin

    2011-10-01

    The effects of organic solvent systems on nail hydration and permeability have not been well studied. The objectives of the present study were to investigate the effects of binary aqueous organic solvent systems of ethanol (EtOH), propylene glycol (PPG), and polyethylene glycol 400 (PEG) on the barrier properties of nail plates. (3) H-water, (14) C-urea, and (14) C-tetraethylammonium ions were the probes in the nail uptake and transport experiments to study the effect(s) of organic solvents on nail hydration and permeability. Gravimetric studies were also performed as a secondary method to study nail hydration and the reversibility of the nail after organic solvent treatments. Both ungual uptake and transport were directly related to the concentration of the organic solvent in the binary systems. Partitioning of the probes into and transport across the nail decreased with an increase in the organic solvent concentration. These changes corresponded to the changes in solution viscosity and the barrier properties of the nail. In general, the effects for PPG and PEG were more pronounced than those for EtOH. Practically, these results suggest that organic solvents in formulations can increase nail barrier resistivity. PMID:21607952

  18. Effects of organic solvents on the barrier properties of human nail.

    Science.gov (United States)

    Smith, Kelly A; Hao, Jinsong; Li, S Kevin

    2011-10-01

    The effects of organic solvent systems on nail hydration and permeability have not been well studied. The objectives of the present study were to investigate the effects of binary aqueous organic solvent systems of ethanol (EtOH), propylene glycol (PPG), and polyethylene glycol 400 (PEG) on the barrier properties of nail plates. (3) H-water, (14) C-urea, and (14) C-tetraethylammonium ions were the probes in the nail uptake and transport experiments to study the effect(s) of organic solvents on nail hydration and permeability. Gravimetric studies were also performed as a secondary method to study nail hydration and the reversibility of the nail after organic solvent treatments. Both ungual uptake and transport were directly related to the concentration of the organic solvent in the binary systems. Partitioning of the probes into and transport across the nail decreased with an increase in the organic solvent concentration. These changes corresponded to the changes in solution viscosity and the barrier properties of the nail. In general, the effects for PPG and PEG were more pronounced than those for EtOH. Practically, these results suggest that organic solvents in formulations can increase nail barrier resistivity.

  19. Effects of UV irradiation and UV/chlorine co-exposure on natural organic matter in water

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Wei; Zhang, Zaili; Yang, Xin; Xu, Yiyue; Liang, Yongmei, E-mail: liangym@mail.sysu.edu.cn

    2012-01-01

    The effects of co-exposure to ultraviolet (UV) irradiation (with either low- or medium-pressure UV lamps) and free chlorine (chloramine) at practical relevant conditions on changes in natural organic matter (NOM) properties were investigated using four waters. The changes were characterized using the specific disinfection by-product formation potential (SDBPFP), specific total organic halogen formation potential (STOXFP), differential UV absorbance ( Increment UVA), and size-exclusion chromatography (SEC). The results for exposure to UV irradiation alone and for samples with no exposure were also obtained. The SDBPFPs in all UV-irradiated NOM waters observed were higher than those of non-irradiated samples. UV irradiation led to increases in STOXFPs as a result of chlorination, but no changes, or only small decreases, from chloramination. UV irradiation alone led to positive Increment UVA spectra of the four NOM waters; co-exposure to UV and chlorine gave larger negative Increment UVA spectra than those obtained by chlorine exposure alone. No obvious changes in SEC results were observed for samples only irradiated with UV light; co-exposure gave no detectable changes in the abundances of small fractions for exposure to chlorine only. Both UV photooxidation and photocatalytic oxidation appear to affect the reactivity of the NOM toward subsequent chlorination, and the magnitude of the changes is generally greater for medium-pressure lamps than for low-pressure lamps. These results suggest that applying UV disinfection technology to a particular source may not always be disinfection by-product-problem-free, and the interactions between UV light, chlorine, and NOM may need to be considered. - Highlights: Black-Right-Pointing-Pointer We discussed the effects of co-exposure to UV light and chlorine on properties of natural organic matters in waters. Black-Right-Pointing-Pointer UV irradiation led to increases in SDBPFP and STOXFP of NOM waters from chlorination. Black

  20. Assessment of Relationship between Spontaneous Abortion and Occupational Exposure to Organic Solvents

    Directory of Open Access Journals (Sweden)

    S Mohammadi

    2011-04-01

    Full Text Available Introduction & Objective: Nowadays, some studies indicate the adverse effects of exposure to chemicals, especially organic solvents on the reproductive system of females. This study aimed to assess the relationship between spontaneous abortion with occupational exposure to organic solvents in pharmaceutical industry. Materials & Methods: This is a cross-sectional and descriptive-analytical study which was carried out in 2010 in one of the pharmaceutical factories located in the suburbs of Tehran. During the study, married women who were working in the factory laboratory units and were exposed to mixed organic solvents were compared with married women who were working in the packing units of the factory without occupational exposure to organic solvents. Frequency of spontaneous abortion and duration of pregnancy were assessed in both two groups. Collected data were analyzed with the SPSS software using t-test, logistic regression, and chi-square test. Results: In the present study, the frequency of spontaneous abortion in employees with exposure to organic solvents mixture was 10.7%. This study showed that even after adjustment for confounding factors, there was a significant correlation between spontaneous abortion and occupational exposure to organic solvents mixture and this correlation increased with increasing levels of exposure to organic solvents. Moreover, a significant correlation was observed between occupational exposure to mixed organic solvents and waiting time to become pregnant (TTP. Furthermore, this study showed that even after adjustment for confounding variables, shift workers were significantly more affected by spontaneous abortion compared to daytime workers (P < 0.001. Conclusion: According to the results of this study, since there is probability of spontaneous abortion resulting from occupational exposure to various chemicals including organic solvents, review of the status of occupational exposure of workers can be helpful

  1. Viscoelastic Properties of Organic Hybrid of Chlorinated Polythylene and Small Molecule

    Institute of Scientific and Technical Information of China (English)

    Chifei Wu

    2000-01-01

    Viscoelastic properties of an organic hybrid of chlorinated polyethylene (CPE) and N,Ndicyclohexyl-benzthiazyl-2-sulfenaamid (DZ) are investigated. All CPE/DZ hybrids show a single loss tangent (Fan δ ) peak. Its position shift linearly to higher temperature and its maximum value increases nonlinearly with increasing DZ content. The energy absorptinity (EA, a ratio of loss modulus to complex modulus) is used to characterize these hybrids. The DZ content dependence of EA changes at a critical value. The existence of a bending point in the DZ content dependence of glass transition temperature and energy absorptinity is due to the microseparation and the crystallization of DZ molecules in CPE/DZ hybrids with high DZ content. The molecular structural model can successfully explain the influence of dispersion state of DZ molecules in the matrix polymer CPE on the maximum value and the position of Tan δ of CPE/DZ hybrids.

  2. Chlorine adlayer-templated growth of a hybrid inorganic-organic layered structure on Au(111)

    Science.gov (United States)

    Rzeźnicka, I. I.; Horino, H.; Yagyu, K.; Suzuki, T.; Kajimoto, S.; Fukumura, H.

    2016-10-01

    Growth of a hybrid inorganic-organic layered structure on the Au(111) surface using a one-step solution growth is reported. The hybrid structure is consist of 4,4‧-bipyridine [4,4‧-BiPyH2]2 + cations, Cl anions and Au adatoms, provided from substrate by means of the adsorbate-induced surface phase transition of a surface reconstruction. Its surface and bulk structures were characterized by scanning tunneling microscopy (STM), secondary ion mass spectrometry (SIMS), and Raman spectroscopy. STM results reveal growth of the first [4,4‧-BiPyH2]2 + layer on top of the p(√{ 3} ×√{ 3})" separators=", R 30 ° chlorine overlayer formed on the Au(111) surface. These two layers are found to provide a platform for a following three-dimensional growth facilitated by hydrogen bonding, aurophilic and π-π stacking interactions.

  3. Screening for organic solvents in Hanford waste tanks using organic vapor concentrations

    Energy Technology Data Exchange (ETDEWEB)

    Huckaby, J.L.; Sklarew, D.S.

    1997-09-01

    The potential ignition of organic liquids stored in the Hanford Site high-level radioactive waste tanks has been identified as a safety issue because expanding gases could potentially affect tank dome integrity. Organic liquid waste has been found in some of the waste tanks, but most are thought to contain only trace amounts. Due to the inhomogeneity of the waste, direct sampling of the tank waste to locate organic liquids may not conclusively demonstrate that a given tank is free of risk. However, organic vapors present above the organic liquid waste can be detected with a high degree of confidence and can be used to identify problem tanks. This report presents the results of a screening test that has been applied to 82 passively ventilated high-level radioactive waste tanks at the Hanford Site to identify those that might contain a significant amount of organic liquid waste. It includes seven tanks not addressed in the previous version of this report, Screening for Organic Solvents in Hanford Waste Tanks Using Total Non-Methane Organic Compound Vapor Concentrations. The screening test is based on a simple model of the tank headspace that estimates the effective surface area of semivolatile organic liquid waste in a tank. Analyses indicate that damage to the tank dome is credible only if the organic liquid burn rate is above a threshold value, and this can occur only if the surface area of organic liquid in a tank is above a corresponding threshold value of about one square meter. Thirteen tanks were identified as potentially containing at least that amount of semivolatile organic liquid based on conservative estimates. Most of the tanks identified as containing potentially significant quantities of organic liquid waste are in the 241-BY and 241-C tank farms, which agrees qualitatively with the fact that these tank farms received the majority of the PUREX process organic wash waste and waste organic liquids.

  4. Effects of Organic Solvents on the Barrier Properties of Human Nail

    OpenAIRE

    Smith, Kelly A; HAO, JINSONG; Li, S. Kevin

    2011-01-01

    The effects of organic solvent systems on nail hydration and permeability have not been well studied. The objectives of the present study were to investigate the effects of binary aqueous organic solvent systems of ethanol (EtOH), propylene glycol (PPG), and polyethylene glycol 400 (PEG) on the barrier properties of nail plates. 3H–water, 14C–urea, and 14C–tetraethylammonium ions were the probes in the nail uptake and transport experiments to study the effect(s) of organic solvents on nail hy...

  5. Chlorinated volatile organic compounds (Cl-VOCs) in environment - sources, potential human health impacts, and current remediation technologies.

    Science.gov (United States)

    Huang, Binbin; Lei, Chao; Wei, Chaohai; Zeng, Guangming

    2014-10-01

    Chlorinated volatile organic compounds (Cl-VOCs), including polychloromethanes, polychloroethanes and polychloroethylenes, are widely used as solvents, degreasing agents and a variety of commercial products. These compounds belong to a group of ubiquitous contaminants that can be found in contaminated soil, air and any kind of fluvial mediums such as groundwater, rivers and lakes. This review presents a summary of the research concerning the production levels and sources of Cl-VOCs, their potential impacts on human health as well as state-of-the-art remediation technologies. Important sources of Cl-VOCs principally include the emissions from industrial processes, the consumption of Cl-VOC-containing products, the disinfection process, as well as improper storage and disposal methods. Human exposure to Cl-VOCs can occur through different routes, including ingestion, inhalation and dermal contact. The toxicological impacts of these compounds have been carefully assessed, and the results demonstrate the potential associations of cancer incidence with exposure to Cl-VOCs. Most Cl-VOCs thus have been listed as priority pollutants by the Ministry of Environmental Protection (MEP) of China, Environmental Protection Agency of the U.S. (U.S. EPA) and European Commission (EC), and are under close monitor and strict control. Yet, more efforts will be put into the epidemiological studies for the risk of human exposure to Cl-VOCs and the exposure level measurements in contaminated sites in the future. State-of-the-art remediation technologies for Cl-VOCs employ non-destructive methods and destructive methods (e.g. thermal incineration, phytoremediation, biodegradation, advanced oxidation processes (AOPs) and reductive dechlorination), whose advantages, drawbacks and future developments are thoroughly discussed in the later sections. PMID:25016450

  6. Why do crown ethers activate enzymes in organic solvents?

    NARCIS (Netherlands)

    Unen, van Dirk-Jan; Engbersen, Johan F.J.; Reinhoudt, David N.

    2002-01-01

    One of the major drawbacks of enzymes in nonaqueous solvents is that their activity is often dramatically low compared to that in water. This limitation can be largely overcome by crown ether treatment of enzymes. In this paper, we describe a number of carefully designed new experiments that have im

  7. Transport, Targeting, and Applications of Metallic Functional Nanoparticles for Degradation of DNAPL Chlorinated Organic Solvents

    Energy Technology Data Exchange (ETDEWEB)

    Gregory V. Lowry; Sara Majetich; Krzysztof Matyjaszewski; David Sholl; Robert Tilton

    2006-12-27

    Dense Non-Aqueous Phase Liquid (DNAPL) such as trichloroethylene act as long term sources of groundwater contaminants and are difficult and expensive to remediate. DNAPL-contaminated sites are a significant financial liability for the Department of Energy and the private sector. The objective of this study was to engineer reactive Fe-based nanoparticles with specialized polymeric coatings to make them mobile in the subsurface and to provide them with an affinity for the DNAPL/water interface. The synthesis, characterization, and reactivity/mobility of the engineered particles, and a molecular dynamic model that predicts their behavior at the DNPAL/water interface are described in this report.

  8. A NOVEL HYDROPHILIC POLYMER MEMBRANE FOR THE DEHYDRATION OF ORGANIC SOLVENTS

    Science.gov (United States)

    Novel hydrophilic polymer membranes based on polyallylamine ydrochloride- polyvinylalcohol are developed. The high selectivity and flux characteristics of these membranes for the dehydration of organic solvents are evaluated using pervaporation technology and are found to be ver...

  9. Organic fragments from graphene oxide: Isolation, characterization and solvent effects

    Indian Academy of Sciences (India)

    Ravula Thirupathi; Y Jayasubba Reddy; Erode N Prabhakaran; Hanudatta S Atreya

    2014-05-01

    As-prepared graphene oxide (GO) contains oxidative debris which can be washed using basic solutions. We present the isolation and characterization of these debris. Dynamic light scattering (DLS) is used to monitor the separation of the debris in various solvents in the presence of different protic and aprotic alkylamino bases. The study reveals that the debris are rich in carbonyl functional groups and water is an essential component for separation and removal of the debris from GO under oxidative reaction conditions.

  10. Enzymatic Synthesis of Dipeptide Derivatives Containing Noncoded Amino Acids in Organic Solvents

    Institute of Scientific and Technical Information of China (English)

    YANG,Hong(杨洪); ZHOU,Chuang(周闯); TIAN,Gui-Ling(田桂玲); YE,Yun-Hua(叶蕴华)

    2002-01-01

    A series of dipeptide derivatives containing non-coded amino acis, N-Boc-4-X-Phe-Ala-NHNHNHPh (X= Cl, Br, I, NO2),were synthesized by using thermoase in organic solvents. The physical data were consistent with the same samples prepared by 3-( diethoxyphosphoryloxy)-1, 2, 3-benzotriazin-4 (3H)-one (DEPBT). Influence of different substituted groups of the non-coded amino acids and different organic solvents on the enzymatic peptide synthesis was studied.

  11. Recurrent Acute Liver Failure Because of Acute Hepatitis Induced by Organic Solvents

    Science.gov (United States)

    Ito, Daisuke; Tanaka, Tomohiro; Akamatsu, Nobuhisa; Ito, Kyoji; Hasegawa, Kiyoshi; Sakamoto, Yoshihiro; Nakagawa, Hayato; Fujinaga, Hidetaka; Kokudo, Norihiro

    2016-01-01

    Abstract The authors present a case of recurrent acute liver failure because of occupational exposure to organic solvents. A 35-year-old man with a 3-week history of worsening jaundice and flu-like symptoms was admitted to our hospital. Viral hepatitis serology and autoimmune factors were negative. The authors considered liver transplantation, but the patient's liver function spontaneously recovered. Liver biopsy revealed massive infiltration of neutrophils, but the cause of the acute hepatitis was not identified. Four months after discharge, the patient's liver function worsened again. The authors considered the possibility of antinuclear antibody-negative autoimmune hepatitis and initiated steroid treatment, which was effective. Four months after discharge, the patient was admitted for repeated liver injury. The authors started him on steroid pulse therapy, but this time it was not effective. Just before the first admission, he had started his own construction company where he was highly exposed to organic solvents, and thus the authors considered organic solvent-induced hepatitis. Although urine test results for organic solvents were negative, a second liver biopsy revealed severe infiltration of neutrophils, compatible with toxic hepatitis. Again, his liver function spontaneously improved. Based on the pathology and detailed clinical course, including the patient's high exposure to organic solvents since just before the first admission, and the spontaneous recovery of his liver damage in the absence of the exposure, he was diagnosed with toxic hepatitis. The authors strongly advised him to avoid organic solvents. Since then, he has been in good health without recurrence. This is the first report of recurrent acute liver failure because of exposure to organic solvents, which was eventually diagnosed through a meticulous medical history and successfully recovered by avoiding the causative agents. In acute liver failure with an undetermined etiology, clinicians

  12. Recurrent Acute Liver Failure Because of Acute Hepatitis Induced by Organic Solvents: A Case Report.

    Science.gov (United States)

    Ito, Daisuke; Tanaka, Tomohiro; Akamatsu, Nobuhisa; Ito, Kyoji; Hasegawa, Kiyoshi; Sakamoto, Yoshihiro; Nakagawa, Hayato; Fujinaga, Hidetaka; Kokudo, Norihiro

    2016-01-01

    The authors present a case of recurrent acute liver failure because of occupational exposure to organic solvents. A 35-year-old man with a 3-week history of worsening jaundice and flu-like symptoms was admitted to our hospital. Viral hepatitis serology and autoimmune factors were negative. The authors considered liver transplantation, but the patient's liver function spontaneously recovered. Liver biopsy revealed massive infiltration of neutrophils, but the cause of the acute hepatitis was not identified. Four months after discharge, the patient's liver function worsened again. The authors considered the possibility of antinuclear antibody-negative autoimmune hepatitis and initiated steroid treatment, which was effective. Four months after discharge, the patient was admitted for repeated liver injury. The authors started him on steroid pulse therapy, but this time it was not effective. Just before the first admission, he had started his own construction company where he was highly exposed to organic solvents, and thus the authors considered organic solvent-induced hepatitis. Although urine test results for organic solvents were negative, a second liver biopsy revealed severe infiltration of neutrophils, compatible with toxic hepatitis. Again, his liver function spontaneously improved. Based on the pathology and detailed clinical course, including the patient's high exposure to organic solvents since just before the first admission, and the spontaneous recovery of his liver damage in the absence of the exposure, he was diagnosed with toxic hepatitis. The authors strongly advised him to avoid organic solvents. Since then, he has been in good health without recurrence. This is the first report of recurrent acute liver failure because of exposure to organic solvents, which was eventually diagnosed through a meticulous medical history and successfully recovered by avoiding the causative agents. In acute liver failure with an undetermined etiology, clinicians should rule

  13. Microbial Consortia Development and Microcosm and Column Experiments for Enhanced Bioremediation of Chlorinated Volatile Organic Compounds, West Branch Canal Creek Wetland Area, Aberdeen Proving Ground, Maryland

    Science.gov (United States)

    Lorah, Michelle M.; Majcher, Emily H.; Jones, Elizabeth J.; Voytek, Mary A.

    2008-01-01

    Chlorinated solvents, including 1,1,2,2-tetrachloroethane, tetrachloroethene, trichloroethene, carbon tetrachloride, and chloroform, are reaching land surface in localized areas of focused ground-water discharge (seeps) in a wetland and tidal creek in the West Branch Canal Creek area, Aberdeen Proving Ground, Maryland. In cooperation with the U.S. Army Garrison, Aberdeen Proving Ground, Maryland, the U.S. Geological Survey is developing enhanced bioremediation methods that simulate the natural anaerobic degradation that occurs without intervention in non-seep areas of the wetland. A combination of natural attenuation and enhanced bioremediation could provide a remedy for the discharging ground-water plumes that would minimize disturbance to the sensitive wetland ecosystem. Biostimulation (addition of organic substrate or nutrients) and bioaugmentation (addition of microbial consortium), applied either by direct injection at depth in the wetland sediments or by construction of a permeable reactive mat at the seep surface, were tested as possible methods to enhance anaerobic degradation in the seep areas. For the first phase of developing enhanced bioremediation methods for the contaminant mixtures in the seeps, laboratory studies were conducted to develop a microbial consortium to degrade 1,1,2,2-tetrachloroethane and its chlorinated daughter products under anaerobic conditions, and to test biostimulation and bioaugmentation of wetland sediment and reactive mat matrices in microcosms. The individual components required for the direct injection and reactive mat methods were then combined in column experiments to test them under groundwater- flow rates and contaminant concentrations observed in the field. Results showed that both direct injection and the reactive mat are promising remediation methods, although the success of direct injection likely would depend on adequately distributing and maintaining organic substrate throughout the wetland sediment in the seep

  14. Geological and hydrogeological features affecting migration, multi-phase partitioning and degradation of chlorinated hydrocarbons through unconsolidated porous media.

    OpenAIRE

    Filippini, Maria

    2015-01-01

    Chlorinated solvents are the most ubiquitous organic contaminants found in groundwater since the last five decades. They generally reach groundwater as Dense Non-Aqueous Phase Liquid (DNAPL). This phase can migrate through aquifers, and also through aquitards, in ways that aqueous contaminants cannot. The complex phase partitioning to which chlorinated solvent DNAPLs can undergo (i.e. to the dissolved, vapor or sorbed phase), as well as their transformations (e.g. degradation), depend on the...

  15. Reactions of aqueous chlorine and chlorine dioxide with model food compounds.

    OpenAIRE

    Fukayama, M Y; Tan, H; Wheeler, W B; Wei, C I

    1986-01-01

    Chlorine and chlorine dioxide (ClO2), common disinfecting and bleaching chemicals used in the food industry, are potent oxidizing and chlorinating agents. Unfortunately, little is known about the nature of the reactions of chlorine with organic food constituents. This presentation reviews published information concerning the reactions of chlorine gas (Cl2[g]), aqueous chlorine, and ClO2 with model food compounds, the fate of chlorine during the chlorination of specific food products, and the ...

  16. Measurement of the collection efficiency and adsorptive distribution of semi and low volatile organic chlorine (SLVOCI) in flue gas

    Energy Technology Data Exchange (ETDEWEB)

    Takakura, A. [Osaka City Institute of Public Health and Environmental Sciences, Osaka (Japan); Watanabe, N.; Minami, Y.; Mizutani, S.; Takatsuki, H. [Kyoto University Environment Preservation Center, Kyoto (Japan)

    2004-09-15

    Municipal waste incineration (MWI) flue gas includes various organic halogen compounds, which show a close correlation between PCDD/Fs concentration and organic halogen group parameters, e.g. TOX and SNVOX. Last year, we reported a newly developed sampling method and atomic emission spectrophotometry system equipped with barrier discharge radio-frequency helium plasma, which detect organic halogen compounds with the advantages of elemental selectivity, high sensitivity and robustness. In this sampling system, flue gas was directed to a two-drain trap and two empty impingers, which removed drain water, hydrochloric acid and moisture (Fig. 1). After those four impingers, semi and low volatile organic halogens (SLVOX) were captured with two different adsorbents. Carbotrap C was the adsorbent for LVOX and Carbotrap B was for SVOX. The flow rate and the sampled gas were 2 L/min and 10-40 L, respectively. In this paper, in order to investigate the passage efficiency through the drain trap and the adsorptive distribution to Carbotrap C and B of various organic chlorinated compounds, chlorinated benzenes (CBs) and chlorinated phenols (CPs) were tested in the sampling system as model organic halogen compounds.

  17. Lignin peroxidase oxidation of aromatic compounds in systems containing organic solvents.

    Science.gov (United States)

    Vazquez-Duhalt, R; Westlake, D W; Fedorak, P M

    1994-02-01

    Lignin peroxidase from Phanerochaete chrysosporium was used to study the oxidation of aromatic compounds, including polycyclic aromatic hydrocarbons and heterocyclic compounds, that are models of moieties of asphaltene molecules. The oxidations were done in systems containing water-miscible organic solvents, including methanol, isopropanol, N, N-dimethylformamide, acetonitrile, and tetrahydrofuran. Of the 20 aromatic compounds tested, 9 were oxidized by lignin peroxidase in the presence of hydrogen peroxide. These included anthracene, 1-, 2-, and 9-methylanthracenes, acenaphthene, fluoranthene, pyrene, carbazole, and dibenzothiophene. Of the compounds studied, lignin peroxidase was able to oxidize those with ionization potentials of stability characteristics of lignin peroxidase were determined by using pyrene as the substrate in systems containing different amounts of organic solvent. Benzyl alkylation of lignin peroxidase improved its activity in a system containing water-miscible organic solvent but did not increase its resistance to inactivation at high solvent concentrations. PMID:16349176

  18. Natural attenuation of chlorinated volatile organic compounds in a freshwater tidal wetland, Aberdeen Proving Ground, Maryland

    Science.gov (United States)

    Lorah, Michelle M.; Olsen, Lisa D.; Smith, Barrett L.; Johnson, Mark A.; Fleck, William B.

    1997-01-01

    Ground-water contaminant plumes that are flowing toward or currently discharging to wetland areas present unique remediation problems because of the hydrologic connections between ground water and surface water and the sensitive habitats in wetlands. Because wetlands typically have a large diversity of microorganisms and redox conditions that could enhance biodegradation, they are ideal environments for natural attenuation of organic contaminants, which is a treatment method that would leave the ecosystem largely undisturbed and be cost effective. During 1992-97, the U.S. Geological Survey investigated the natural attenuation of chlorinated volatile organic compounds (VOC's) in a contaminant plume that discharges from a sand aquifer to a freshwater tidal wetland along the West Branch Canal Creek at Aberdeen Proving Ground, Maryland. Characterization of the hydrogeology and geochemistry along flowpaths in the wetland area and determination of the occurrence and rates of biodegradation and sorption show that natural attenuation could be a feasible remediation method for the contaminant plume that extends along the West Branch Canal Creek.

  19. Probing Contaminant Transport to and from Clay Surfaces in Organic Solvents and Water Using Solution Calorimetry.

    Science.gov (United States)

    Pourmohammadbagher, Amin; Shaw, John M

    2015-09-15

    Clays, in tailings, are a significant ongoing environmental concern in the mining and oilsands production industries, and clay rehabilitation following contamination poses challenges episodically. Understanding the fundamentals of clay behavior can lead to better environmental impact mitigation strategies. Systematic calorimetric measurements are shown to provide a framework for parsing the synergistic and antagonistic impacts of trace (i.e., parts per million level) components on the surface compositions of clays. The enthalpy of solution of as-received and "contaminated" clays, in as-received and "contaminated" organic solvents and water, at 60 °C and atmospheric pressure, provides important illustrative examples. Clay contamination included pre-saturation of clays with water and organic liquids. Solvent contamination included the addition of trace water to organic solvents and trace organic liquids to water. Enthalpy of solution outcomes are interpreted using a quantitative mass and energy balance modeling framework that isolates terms for solvent and trace contaminant sorption/desorption and surface energy effects. Underlying surface energies are shown to dominate the energetics of the solvent-clay interaction, and organic liquids as solvents or as trace contaminants are shown to displace water from as-received clay surfaces. This approach can be readily extended to include pH, salts, or other effects and is expected to provide mechanistic and quantitative insights underlying the stability of clays in tailings ponds and the behaviors of clays in diverse industrial and natural environments. PMID:26296102

  20. Revisiting the effects of organic solvents on the thermal reduction of graphite oxide

    Energy Technology Data Exchange (ETDEWEB)

    Barroso-Bujans, Fabienne, E-mail: fbarroso@ehu.es [Centro de Fisica de Materiales-Material Physics Center (CSIC-UPV/EHU), Paseo Manuel Lardizabal 5, 20018 San Sebastian (Spain); Fierro, Jose Luis G. [Instituto de Catalisis y Petroleoquimica, CSIC. Marie Curie, 2, Cantoblanco, 28049 Madrid (Spain); Alegria, Angel [Centro de Fisica de Materiales-Material Physics Center (CSIC-UPV/EHU), Paseo Manuel Lardizabal 5, 20018 San Sebastian (Spain); Departamento de Fisica de Materiales, Universidad del Pais Vasco (UPV/EHU) Apartado 1072, 20080 San Sebastian (Spain); Colmenero, Juan [Centro de Fisica de Materiales-Material Physics Center (CSIC-UPV/EHU), Paseo Manuel Lardizabal 5, 20018 San Sebastian (Spain); Departamento de Fisica de Materiales, Universidad del Pais Vasco (UPV/EHU) Apartado 1072, 20080 San Sebastian (Spain); Donostia International Physics Center, Paseo Manuel Lardizabal 4, 20018 San Sebastian (Spain)

    2011-11-10

    Highlights: Black-Right-Pointing-Pointer Retention of organic solvent on graphite oxide interlayer space. Black-Right-Pointing-Pointer Decreasing exfoliation temperature. Black-Right-Pointing-Pointer Close link between structure and thermal behavior of solvent treated graphite oxide. Black-Right-Pointing-Pointer Restacking inhibition of thermally reduced graphite oxide sheets. Black-Right-Pointing-Pointer Changes in kinetic mechanisms of thermal reduction. - Abstract: Treatment of graphite oxide (GO) with organic solvents via sorption from either liquid or gas phase, and subsequent desorption, induces profound changes in the layered GO structure: loss of stacking order, retention of trace amounts of solvents and decreasing decomposition temperature. This study presents new evidences of the effect of organic solvents on the thermal reduction of GO by means of thermogravimetric analysis, X-ray diffraction and X-ray photoelectron spectroscopy. The results reveal a relative higher decrease of the oxygen amounts in solvent-treated GO as compared to untreated GO and the restacking inhibition of the thermally reduced GO sheets upon slow heating. The kinetic experiments evidence changes occurring in the reduction mechanisms of the solvent-treated GO, which support the close link between GO structure and thermal properties.

  1. IN-SITU DUOX™ CHEMICAL OXIDATION TECHNOLOGY TO TREAT CHLORINATED ORGANICS AT THE ROOSEVELT MILLS SITE, VERNON, CT: SITE CHARACTERIZATION AND TREATABILITY STUDY

    Science.gov (United States)

    A study was performed investigating the feasibility of applying the DUOX™ chemical oxidation technology to chlorinated solvent contaminated media at the Roosevelt Mills site in Vernon, Connecticut. The Roosevelt Mills site is a former woolen mill that included dry cleaning operat...

  2. Reaction products of chlorine dioxide.

    OpenAIRE

    Stevens, A A

    1982-01-01

    Inspection of the available literature reveals that a detailed investigation of the aqueous organic chemistry of chlorine dioxide and systematic identification of products formed during water disinfection has not been considered. This must be done before an informed assessment can be made of the relative safety of using chlorine dioxide as a disinfectant alternative to chlorine. Although trihalomethanes are generally not formed by the action of chlorine dioxide, the products of chlorine dioxi...

  3. Measurement and prediction of aromatic solute distribution coefficients for aqueous-organic solvent systems. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Campbell, J.R.; Luthy, R.G.

    1984-06-01

    Experimental and modeling activities were performed to assess techniques for measurement and prediction of distribution coefficients for aromatic solutes between water and immiscible organic solvents. Experiments were performed to measure distribution coefficients in both clean water and wastewater systems, and to assess treatment of a wastewater by solvent extraction. The theoretical portions of this investigation were directed towards development of techniques for prediction of solute-solvent/water distribution coefficients. Experiments were performed to assess treatment of a phenolic-laden coal conversion wastewater by solvent extraction. The results showed that solvent extraction for recovery of phenolic material offered several wastewater processing advantages. Distribution coefficients were measured in clean water and wastewater systems for aromatic solutes of varying functionality with different solvent types. It was found that distribution coefficients for these compounds in clean water systems were not statistically different from distribution coefficients determined in a complex coal conversion process wastewater. These and other aromatic solute distribution coefficient data were employed for evaluation of modeling techniques for prediction of solute-solvent/water distribution coefficients. Eight solvents were selected in order to represent various chemical classes: toluene and benzene (aromatics), hexane and heptane (alkanes), n-octanol (alcohols), n-butyl acetate (esters), diisopropyl ether (ethers), and methylisobutyl ketone (ketones). The aromatic solutes included: nonpolar compounds such as benzene, toluene and naphthalene, phenolic compounds such as phenol, cresol and catechol, nitrogenous aromatics such as aniline, pyridine and aminonaphthalene, and other aromatic solutes such as naphthol, quinolinol and halogenated compounds. 100 references, 20 figures, 34 tables.

  4. Structure of Solvent-Free Nanoparticle−Organic Hybrid Materials

    KAUST Repository

    Yu, Hsiu-Yu

    2010-11-16

    We derive the radial distribution function and the static structure factor for the particles in model nanoparticleorganic hybrid materials composed of nanoparticles and attached oligomeric chains in the absence of an intervening solvent. The assumption that the oligomers form an incompressible fluid of bead-chains attached to the particles that is at equilibrium for a given particle configuration allows us to apply a density functional theory for determining the equilibrium configuration of oligomers as well as the distribution function of the particles. A quasi-analytic solution is facilitated by a regular perturbation analysis valid when the oligomer radius of gyration R g is much greater than the particle radius a. The results show that the constraint that each particle carries its own share of the fluid attached to itself yields a static structure factor that approaches zero as the wavenumber approaches zero. This result indicates that each particle excludes exactly one other particle from its neighborhood. © 2010 American Chemical Society.

  5. Non-Hodgkin's lymphoma risk derived from exposure to organic solvents: a review of epidemiologic studies

    Directory of Open Access Journals (Sweden)

    Rêgo Marco Antônio V.

    1998-01-01

    Full Text Available The rate of non-Hodgkin's lymphomas (NHL has increased around the world during the last decades. Apart from the role of the human immunodeficiency virus (HIV infection in the development of NHL, exposure to chemical agents like phenoxyacetic pesticides, hair dyes, metal fumes and organic solvents are suspected to be involved. The present review evaluates the results of studies that directly or indirectly searched for an association between solvent exposure and NHL. The selected studies comprised those published from 1979 to 1997, designed to investigate risk factors for NHL, whether specifically looking for solvent exposure or for general risks in which solvent exposure could be included. In 25 of the 45 reviewed studies (55.5%, fifty-four statistically significant associations between NHL and solvent exposure related occupations or industries were reported. Statistical significance was more frequently shown in studies where solvent exposure was more accurately defined. In eighteen of such studies, 13 (72.2% defined or suggested organic solvents as possible risk factors for NHL.

  6. Organic Solvents Mediate Self-assembly of GAV-9 Peptide on Mica Surface

    Institute of Scientific and Technical Information of China (English)

    Hai LI; Feng ZHANG; Yi ZHANG; Jianhua HE; Jun HU

    2007-01-01

    Self-assembly of peptides into fibrils and other morphologies has attracted much attention in many fields, especially in nanofabrication, pathology and biochemistry. In this paper, self-assembly of GAV-9 peptide in organic solvents, ethanol and acetone, was investigated using atomic force microscopy (AFM)and attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR). The results indicated that GAV-9 self- assembled into various nanostructures in both solvents after deposited and evaporated on mica. Fibrils with β-sheet conformation were observed in both solvents when the peptide concentration was higher than 280 μM. However, ordered fibrils with β-sheet conformation were formed in ethanol, but not in acetone, with a peptide concentration ranging from 7 μM to 28 μM. We attribute the formation of various nanostructures to the different physicochemical properties of the polar organic solvents on the self-assembly of GAV-9 peptide.

  7. The chlorination of cyclopentanone and cyclohexanone

    NARCIS (Netherlands)

    Maatman, Hendrik

    1980-01-01

    In this thesis the results of an investigation of the chlorination of cyclopentanone and cyclohexanone in the solvent carbontetrachloride and catalyzed by hydrogen chloride are described. ... Zie: Summary

  8. Remediation of soils, sediments and sludges by extraction with organic solvents

    OpenAIRE

    Noordkamp, E.

    1999-01-01

    Remediation of contaminated soils, sediments and sludges by extraction with organic solvents is still in the initial stages of development. So far hardly any scientific research has been carried out into this approach. Therefore, the main objective of the present investigation was to study the effect of several process parameters on the efficiency of the extraction step of a solvent extraction process for soils, sediments and sludges (generally indicated as solids) contaminated with polycycli...

  9. Aggregation behavior of cholic acid derivatives in organic solvents and in water

    OpenAIRE

    Willemen, H.M.

    2002-01-01

    In this thesis various cholic acid derivatives are reported that display aggregation in water or in organic solvents. Spontaneous aggregation of single molecules into larger, ordered structures occurs at the borderline of solubility. Amphiphilic compounds, or surfactants, which possess a hydrophobic as well as a hydrophilic part, have a high tendency to form aggregates to minimize unfavorable polar-apolar interactions with the surrounding solvent. There are different types of aggregates in wa...

  10. Application of in situ chemical oxidation technique with potassium permanganate for the remediation of a shallow aquifer contaminated with chlorinated solvents

    Directory of Open Access Journals (Sweden)

    Alaine Santos da Cunha

    2012-12-01

    Full Text Available In situ chemical oxidation is a method that is frequently being used for the remediation of contaminated areas, since it presents an adequate efficiency in the reduction of the contaminant mass, particularly chlorinated ethenes, in a relatively short period of time. This manuscript presents the results of the application of this method, using the injection of potassium permanganate as the remediation agent, in an impacted area with chlorinated organic compounds, especially 1,1-dichloroethene. The effectiveness of this remediation method is related to the complexity of the conceptual model of the contaminated site and to the conduction of specific studies in laboratory and pilot tests in field scale, prior to the accomplishment of the full-scale remediation. Therefore, this work contributes presenting a description of the procedures that are commonly used for conducting this kind of studies. In the case under study, it was estimated that the mass of 1.1-dichloroethene (1.1-DCE was reduced from 15.53 to 1.81 kg in groundwater 22 months after the injection of potassium permanganate in the aquifer. The average concentrations of 1.1-DCE in groundwater decreased from 200 to 24 g/L, which value is lower than the environmental standard limit and also to the calculated target of remediation based on human-health risk assessment. Significant contamination rebounds were not identified in the aquifer after the injection of the chemical oxidant. The suitable results of the remediation in this case may be related to the relatively low aquifer heterogeneity and low original concentrations of the contaminant.

  11. Prechlorination of algae-laden water: The effects of transportation time on cell integrity, algal organic matter release, and chlorinated disinfection byproduct formation.

    Science.gov (United States)

    Qi, Jing; Lan, Huachun; Liu, Ruiping; Miao, Shiyu; Liu, Huijuan; Qu, Jiuhui

    2016-10-01

    The prechlorination-induced algal organic matter (AOM) released from Microcystis aeruginosa (M. aeruginosa) cells has been reported to serve as a source of precursors for chlorinated disinfection byproducts (DBPs). However, previous studies have mainly focused on the precursors either extracted directly from the cell suspension or derived immediately after algal suspension prechlorination. This study aims to investigate the impacts of water transportation time after algal suspension prechlorination on cell integrity, AOM release, and DBP formation during the dissolved phase chlorination. The damage to cell integrity after prechlorination was indicated to depend not only on chlorine dose but also on transportation time. The highest dissolved organic carbon (DOC) and dissolved organic nitrogen (DON) values were observed at 2 mg/L chlorine preoxidation before transportation, but were obtained at 0.4 mg/L chlorine after 480-min simulated transportation. The variation of DON with transportation time was indicated to be mainly influenced by the small molecular weight nitrogenous organic compounds, such as amino acids. Additionally, formation of the corresponding chlorinated carbonaceous disinfection byproducts (C-DBPs) and nitrogenous disinfection byproducts (N-DBPs) during the dissolved phase chlorination showed the same variation tendency as DOC and DON respectively. The highest C-DBP (98.4 μg/L) and N-DBP (5.5 μg/L) values were obtained at 0.4 mg/L chlorine preoxidation after 480-min simulated transportation. Therefore, when prechlorination is applied for algae-laden water pretreatment, not only chlorine dose but also transportation time needs to be considered with regard to their effects on cell integrity, AOM release, and chlorinated DBP formation.

  12. Prechlorination of algae-laden water: The effects of transportation time on cell integrity, algal organic matter release, and chlorinated disinfection byproduct formation.

    Science.gov (United States)

    Qi, Jing; Lan, Huachun; Liu, Ruiping; Miao, Shiyu; Liu, Huijuan; Qu, Jiuhui

    2016-10-01

    The prechlorination-induced algal organic matter (AOM) released from Microcystis aeruginosa (M. aeruginosa) cells has been reported to serve as a source of precursors for chlorinated disinfection byproducts (DBPs). However, previous studies have mainly focused on the precursors either extracted directly from the cell suspension or derived immediately after algal suspension prechlorination. This study aims to investigate the impacts of water transportation time after algal suspension prechlorination on cell integrity, AOM release, and DBP formation during the dissolved phase chlorination. The damage to cell integrity after prechlorination was indicated to depend not only on chlorine dose but also on transportation time. The highest dissolved organic carbon (DOC) and dissolved organic nitrogen (DON) values were observed at 2 mg/L chlorine preoxidation before transportation, but were obtained at 0.4 mg/L chlorine after 480-min simulated transportation. The variation of DON with transportation time was indicated to be mainly influenced by the small molecular weight nitrogenous organic compounds, such as amino acids. Additionally, formation of the corresponding chlorinated carbonaceous disinfection byproducts (C-DBPs) and nitrogenous disinfection byproducts (N-DBPs) during the dissolved phase chlorination showed the same variation tendency as DOC and DON respectively. The highest C-DBP (98.4 μg/L) and N-DBP (5.5 μg/L) values were obtained at 0.4 mg/L chlorine preoxidation after 480-min simulated transportation. Therefore, when prechlorination is applied for algae-laden water pretreatment, not only chlorine dose but also transportation time needs to be considered with regard to their effects on cell integrity, AOM release, and chlorinated DBP formation. PMID:27348194

  13. [Sensing characteristics of a real-time monitor using a photoionization detector on organic solvent vapors].

    Science.gov (United States)

    Hori, Hajime; Ishematsu, Sumiyo; Fueta, Yukiko; Hinoue, Mitsuo; Ishidao, Toru

    2012-12-01

    Measurements of organic solvents in the work environment are carried out by either direct sampling using plastic bags/gas chromatography, solid sorbent adsorption using charcoal tubes/gas chromatography, or by a direct reading method using detector tubes. However, these methods cannot always measure the work environment accurately because the concentration of hazardous materials changes from time to time, and from space to space. In this study, the sensor characteristics of a real time monitor using a photoionization detector that can monitor vapor concentration continuously were investigated for 52 organic solvent vapors that are required to be measured in the work environment by the Ordinance of Organic Solvent Poisoning Prevention in Japan. The sensitivity of the monitor was high for the solvents with low ionization potential. However, the sensitivity for the solvents with high ionization potential was low, and the sensor could not detected 7 solvents. Calibration of the sensor using a standard gas was desirable before being used for measurement because the sensitivity of the sensor was variable. PMID:23270260

  14. Catalytic hydrogen-chlorine exchange between chlorinated hydrocarbons under oxygen-free conditions

    NARCIS (Netherlands)

    van der Heijden, A.W.A.M.; Podkolzin, S.G.; Jones, M.E.; Bitter, J.H.; Weckhuysen, B.M.

    2008-01-01

    Chlorinated hydrocarbons (CHCs) remain important industrial chemical intermediates and solvents, especially for the exploration of the potential of La-based materials for the conversion of chlorinated waste compounds.[1] The production of industrially important CHCs frequently occurs with concurrent

  15. Incineration of contaminated organic solvents in a fluidized-bed calciner

    International Nuclear Information System (INIS)

    The reprocessing of expended reactor fuels at the Idaho Chemical Processing Plant (ICPP) generates contaminated organic solvents. An evaluation of potential management alternatives shows that several are suitable for management of contaminated solvents containing tri-butyl phosphate (TBP): the solvent could be burned in a commercially-available burner which absorbs the phosphorus on a fluidized-bed of limestone leaving a solid product for burial; the solvent could be burned in a small fluidized-bed calciner which solidifies non-radioactive feed by in-bed combustion of the contaminated solvent. The fluidized-bed absorbs the phosphate forming a solid product for burial; the solvents could be solidified with a gel or sorbant for burial if the reprocessing system were modified to reduce the solvent volume; and the contaminated solvent could be burned in an existing fluidized-bed calciner designed for solidifying high-level aqueous wastes. Burning the solvent in the existing calciner was selected for process verification because it provides an existing burner, off-gas system, and solids transfer and storage system. No additional wastes are generated. A set of four pilot-plant tests verified the absence of adverse effects from the phosphorus in the fuel when calcining simulated ICPP aqueous wastes. Essentially all of the phosphorus remained in the calcined solids with only a neglegible quantity remaining in the scrubbed off-gas. Combustion efficiency was high (93 to 96%). There were no observable adverse effects on solids in the scrubbing system, corrosion rates, or solids flowability (for retrieval). Conclusions of general applicability are: alternative technologies are available for disposal of contaminated solvents, and the use of an existing fuel-using facility, e.g., calciner or incinerator - designed for contaminated wastes will usually be cost effective

  16. Solvent-resistant organic transistors and thermally stable organic photovoltaics based on cross-linkable conjugated polymers

    KAUST Repository

    Kim, Hyeongjun

    2012-01-10

    Conjugated polymers, in general, are unstable when exposed to air, solvent, or thermal treatment, and these challenges limit their practical applications. Therefore, it is of great importance to develop new materials or methodologies that can enable organic electronics with air stability, solvent resistance, and thermal stability. Herein, we have developed a simple but powerful approach to achieve solvent-resistant and thermally stable organic electronic devices with a remarkably improved air stability, by introducing an azide cross-linkable group into a conjugated polymer. To demonstrate this concept, we have synthesized polythiophene with azide groups attached to end of the alkyl chain (P3HT-azide). Photo-cross-linking of P3HT-azide copolymers dramatically improves the solvent resistance of the active layer without disrupting the molecular ordering and charge transport. This is the first demonstration of solvent-resistant organic transistors. Furthermore, the bulk-heterojunction organic photovoltaics (BHJ OPVs) containing P3HT-azide copolymers show an average efficiency higher than 3.3% after 40 h annealing at an elevated temperature of 150 °C, which represents one of the most thermally stable OPV devices reported to date. This enhanced stability is due to an in situ compatibilizer that forms at the P3HT/PCBM interface and suppresses macrophase separation. Our approach paves a way toward organic electronics with robust and stable operations. © 2011 American Chemical Society.

  17. Normal serum activities of liver enzymes in Swedish paint industry workers with heavy exposure to organic solvents

    Energy Technology Data Exchange (ETDEWEB)

    Lundberg, I.; Hakansson, M.

    1985-09-01

    The serum activities of the liver enzymes alanine aminotransferase, aspartate aminotransferase, ornithine carbamyl transferase, and gamma-glutamyl transferase were examined in 47 paint industry workers and unexposed age matched referents. The workers were exposed to a mixture of industrial solvents, of which xylene was the main component in most cases. The median total exposure was about 50% of Swedish 1981 threshold limit values according to measurements of individual solvent exposure performed at the same time. No differences in enzyme activities were shown either when the whole exposed and referent groups were compared or when the five workers with outstanding solvent exposures of five times the TLV or more were compared with their referents. It is concluded that in most workers the liver seems to remain largely undamaged from inhalation exposure to a commonly used mixture of non-chlorinated solvents. In many workers this seems to hold true even for high exposures for limited periods.

  18. Removal of ion-implanted photoresists on GaAs using two organic solvents in sequence

    Science.gov (United States)

    Oh, Eunseok; Na, Jihoon; Lee, Seunghyo; Lim, Sangwoo

    2016-07-01

    Organic solvents can effectively remove photoresists on III-V channels without damage or etching of the channel material during the process. In this study, a two-step sequential photoresist removal process using two different organic solvents was developed to remove implanted ArF and KrF photoresists at room temperature. The effects of organic solvents with either low molar volumes or high affinities for photoresists were evaluated to find a proper combination that can effectively remove high-dose implanted photoresists without damaging GaAs surfaces. The performance of formamide, acetonitrile, nitromethane, and monoethanolamine for the removal of ion-implanted ArF and KrF photoresists were compared using a two-step sequential photoresist removal process followed by treatment in dimethyl sulfoxide (DMSO). Among the various combinations, the acetonitrile + DMSO two-step sequence exhibited the best removal of photoresists that underwent ion implantation at doses of 5 × 1013-5 × 1015 atoms/cm2 on both flat and trench-structured GaAs surfaces. The ability of the two-step process using organic solvents to remove the photoresists can be explained by considering the affinities of solvents for a polymer and its permeability through the photoresist.

  19. Synthesis of levan in water-miscible organic solvents.

    Science.gov (United States)

    Castillo, E; López-Munguía, A

    2004-10-19

    The synthesis of levan using a levansucrase from a strain of Bacillus subtilis was studied in the presence of the water-miscible solvents: acetone, acetonitrile and 2-methyl-2-propanol (2M2P). It was found that while the enzyme activity is only slightly affected by acetone and acetonitrile, 2M2P has an activating effect increasing the total activity 35% in 40-50% (v/v) 2M2P solutions at 30 degrees C. The enzyme is highly stable in water at 30 degrees C; however, incubation in the presence of 15 and 50% (v/v) 2M2P reduced the half-life time to 23.6 and 1.8 days, respectively. This effect is reversed in 83% 2M2P, where a half-life time of 11.8 days is observed. The presence of 2M2P in the system increases the transfer/hydrolysis ratio of levansucrase. As the reaction proceeds with 10% (w/v) sucrose in 50/50 water/2M2P sucrose is converted to levan and an aqueous two-phase system (2M2P/Levan) is formed and more sucrose can be added in a fed batch mode. It is shown that high molecular weight levan is obtained as an hydrogel and may be easily recovered from the reaction medium. However, when high initial sucrose concentrations (40% (w/v) in 50/50 water/2M2P) are used, an aqueous two-phase system (2M2P/sucrose) is induce, where the synthesized levan has a similar molecular weight distribution as in water and remains in solution. PMID:15464614

  20. Preparation of graphene sponge by vapor phase reduction for oil and organic solvent removal

    Science.gov (United States)

    Wu, Ruihan; Yu, Baowei; Jin, Xinyan; Liu, Xiaoyang; Bai, Yitong; Chen, Lingyun; Ming, Zhu; Yang, Hua; Yang, Sheng-Tao; Luo, Jianbin

    2016-10-01

    Due to the porous structure and hydrophobicity, graphene sponge has huge adsorption capacity for oils and organic solvents. In this study, we reported that graphene sponge could be prepared by vapor phase reduction (denoted as VPRGS) for oil and organic solvent removal. Graphene oxide was lyophilized and reduced by steamy hydrazine hydrate to produce VPRGS. VPRGS had huge capacity for oils and organic solvents (72–224 g g‑1). In particular, the adsorption capacity for crude oil reached 165 g g‑1, suggesting that VPRGS could be applied in oil leakage remediation. VPRGS could treat pollutants both in pure liquid form and in the simulated sea water, where the hydrophobic nature of VPRGS allowed the floating of VPRGS on simulated sea water. VPRGS could be easily regenerated without obvious capacity loss up to 9 cycles. The implications to the applications of VPRGS in oil/water separation and water remediation are discussed.

  1. [Formation of disinfection by-products by Microcystis aeruginosa intracellular organic matter: comparison between chlorination and bromination].

    Science.gov (United States)

    Tian, Chuan; Guo, Ting-Ting; Liu, Rui-Ping; Jefferson, William; Liu, Hui-Juan; Qu, Jiu-Hui

    2013-11-01

    In order to illustrate the effects of released algal organic matter in cyanobacteria blooms on raw water quality and water treatment process, intracellular organic matter (IOM) of Microcystis aeruginosa, which is the dominant species in cyanobacteria blooms, was chosen as a precursor and characterized. In addition, the transformation of IOM and the formation of disinfection byproducts were evaluated at different pH of 6.5, 7.1 and 8.4 after chlorination or bromination, with subsequent correlation analysis. The results indicated that IOM was primarily composed of macromolecular matter, i. e. , the species with relative molecular weight of > 30 x 10(3), constituting 68.8% of dissolved organic carbon (DOC). Fluorescence excitation-emission matrix indicated that IOM was mainly composed of aromatic protein-like matter with an intensity of 92.6 AU x L x mg(-1). After reaction with chlorine or bromine, the intensity of aromatic protein-like peaks decreased sharply by 76.6% - 93.3%, and its reduction correlated well with the formation of trihalomethane (THMs, R2 = 0.81) and haloacetic acid (HAAs, R2 = 0.77). The formation of THMs and HAAs increased with the increase in pH. Compared with chlorine, bromine formed more THMs and HAAs, and tended to form highly halogenated HAAs. However, with increasing pH, the reactivity with IOM between chlorine and bromine was closer, i.e, k(OBr-IOM)/k(OCl-(IOM) < k(HOBr-IOM/k(HOCl-IOM).

  2. Crosslinked copolyazoles with a zwitterionic structure for organic solvent resistant membranes

    KAUST Repository

    Chisca, Stefan

    2015-01-01

    The preparation of crosslinked membranes with a zwitterionic structure based on a facile reaction between a newly synthesized copolyazole with free OH groups and (3-glycidyloxypropyl)trimethoxysilane (GPTMS) is reported. The new OH-functionalized copolyazole is soluble in common organic solvents, such as tetrahydrofuran (THF), dimethylsulfoxide (DMSO), N,N′-dimethylformamide (DMF) and N-methyl-2-pyrrolidone (NMP) and can be easily processed by phase inversion. After crosslinking with GPTMS, the membranes acquire high solvent resistance. We show the membrane performance and the influence of the crosslinking reaction conditions on the thermal stability, surface polarity, pore morphology, and solvent resistance. By using UV-spectroscopy we monitored the solvent resistance of the membranes in four aggressive solvents (THF, DMSO, DMF and NMP) for 30 days. After this time, only minor changes (less than 2%) were detected for membranes subjected to a crosslinking reaction for 6 hours or longer. Our data suggest that the novel crosslinked membranes can be used for industrial applications in wide harsh environments in the presence of organic solvents.

  3. Molecular transport behaviour of organic solvents through halloysite nanotubes filled ethylene–vinyl acetate copolymer

    Indian Academy of Sciences (India)

    Suvendu Padhi; P Ganga Raju Achary; Nimai C Nayak

    2015-08-01

    The transport behaviour of three organic solvents (benzene, toluene and xylene) through halloysite nanotubes (HNTs) filled ethylene–vinyl acetate (EVA) copolymer composites have been investigated in the temperature range 303–323 K. The effects of HNTs loading, nature of solvent and temperature on the transport behaviour of solvents through composites were studied. It has been observed that all the systems follow a Fickian mode of transport on increasing temperature. The solvent uptake and sorption coefficient decreases with the increase in halloysite loading while diffusion coefficients and permeation coefficients were found to be dependent on the concentration of filler. The percentage of bounds rubber content and swelling ratio decreases up to 7.5 phr filler content, whereas above 7.5 phr filler loading were found to be increased due to poor dispersion of halloysite in EVA copolymer matrix. The transport behaviour of three organic solvents was further validated by their crosslink density values. The thermodynamic parameters such as enthalpy, entropy and free energy of sorption were evaluated. The positive values of free energy indicate the non-spontaneity of the sorption of HNTs filled EVA in aromatic solvents at 303 K.

  4. Plasma-polymerized films providing selective affinity to the polarity of vaporized organic solvents

    International Nuclear Information System (INIS)

    Plasma-polymerized films (PPFs) were fabricated as recognition membranes for a vapor-sensing device, and their affinity to vaporized organic solvents was evaluated with surface plasmon resonance. The affinity we intended to create is the selective sorption of the vaporized organic solvents depending on their polarity. For this purpose, acetonitrile, ethylenediamine (EDA), styrene, hexamethyldisiloxane (HMDSO), and hexamethyldisilazane were used to fabricate PPFs. Vaporized methanol, ethanol, and 1-propanol were used as high-polar solvents to be analyzed. Hexane, toluene, and p-xylene were used as low-polar solvents. As a result, the HMDSO-PPF with 97.3o of contact angle was found to provide affinity to the low-polar solvents. In contrast, the EDA-PPF with 7.1o of contact angle provided affinity to the high-polar solvents. Observations of the surface morphology of the HMDSO- and EDA-PPFs with a scanning electron microscope revealed that they are composed of nano-scale islands.

  5. On enzymatic activity in organic solvents as a function of enzyme history

    Energy Technology Data Exchange (ETDEWEB)

    Ke, T.; Klibanov, A.M. [Massachusetts Inst. of Tech., Cambridge, MA (United States). Dept. of Chemistry

    1998-03-20

    Catalytic activities of {alpha}-chymotrypsin and subtilisin Carlsberg in various hydrous organic solvents were measured as a function of how the enzyme suspension had been prepared. In one method, lyophilized enzyme was directly suspended in the solvent containing 1% water. In another, the enzyme was precipitated from its aqueous solution by a 100-fold dilution with an anhydrous solvent. In most cases, the reaction rate in a given nonaqueous enzymatic system strongly (up to an order of magnitude) depended on the mode of enzyme preparation. The magnitude of this dependence was markedly affected by the nature of the solvent and enzyme. A mechanistic hypothesis proposed to explain the observed dependencies was verified in additional experiments in which the water contents and enzyme history were further varied.

  6. Azeotropic binary solvent mixtures for preparation of organic single crystals

    NARCIS (Netherlands)

    Li, X.; Kjellander, B.K.C.; Anthony, J.E.; Bastiaansen, C.W.M.; Broer, D.J.; Gelinck, G.H.

    2009-01-01

    Here, a new approach is introduced to prepare large single crystals of π-conjugated organic molecules from solution. Utilizing the concept of azeotropism, single crystals of tri-isopropylsilylethynyl pentacene (TIPS-PEN) with dimensions up to millimeters are facilely self-assembled from homogeneous

  7. Reactions of metallic Li or LiC6 with organic solvents for lithium ion battery

    Science.gov (United States)

    Nakajima, Tsuyoshi; Hirobayashi, Yuki; Takayanagi, Yuki; Ohzawa, Yoshimi

    2013-12-01

    DSC (Differential Scanning Calorimetry) study has been made on the reactions of metallic Li or LiC6 with organic solvents for lithium ion battery. Ethylene carbonate (EC) more easily reacts with metallic Li and LiC6 than propylene carbonate (PC). This may be because formation of lithium alkyl carbonate is more difficult for PC than EC. On the other hand, diethyl carbonate (DEC), ethyl methyl carbonate (EMC) and dimethyl carbonate (DMC) react with Li in the same manner. Reactions of Li and LiC6 with organic solvents have been discussed based on the results of quantum calculation.

  8. Quantitative determination of urinary metabolites in subjects exposed to organic solvents.

    Directory of Open Access Journals (Sweden)

    Ogata,Masana

    1981-12-01

    Full Text Available Most of the common organic solvents are excreted into urine as metabolites. A correlation exists for several organic solvents between the amount taken in and the amount of metabolites excreted. Many methods have been developed for the measurement of these urinary metabolites. The methods were classified into three group: colorimetry, gas chromatography and high performance liquid chromatography. The characteristics and availability of these methods in a laboratory for routine work were reviewed. The correction equation for the amounts of metabolites in spot urine is discussed.

  9. Substitution of Organic Solvents - a Way to improve Working Environment and reduce Emissions to the Atmosphere

    DEFF Research Database (Denmark)

    Jacobsen, Thomas

    1996-01-01

    Often there is a conflict between considerations regarding the working environment, and considerations regarding the environment, locally and globally, outside the company. When processes involving use of volatile, organic solvents are closely analyzed, it may in many cases be possible to change...... the process in order to omit the solvents or to use water-based products. In cases, where a change to water-based is not evident, improvements can be reached by using non-volatile, low-toxic products, typically esters of fatty acids from vegetable oils. In offset printing a drastic reduction of use of organic...

  10. Organic solvents-free technique for determining sulfadimethoxine and its metabolites in chicken meat.

    Science.gov (United States)

    Furusawa, Naoto

    2007-11-16

    A quick and cost-effective technique of sample preparation followed by a reversed-phase high performance liquid chromatography under "organic solvent-free" (=100% aqueous) conditions for the simultaneous quantifying of sulfadimethoxine (SDM) and its metabolites, 6-hydroxy SDM (6-OH) and N(4)-acetyl SDM (N(4)-Ac), in chicken muscle is presented. Analysis by HPLC with photo-diode array detector was performed using a short C1 column with an isocratic 0.04 mol/l citric acid mobile phase. The method was validated by the analyses of spiked chicken muscle samples, resulting recoveries (> or =84%; relative standard deviations organic solvents were used at all.

  11. Toxicity on aquatic organisms exposed to secondary effluent disinfected with chlorine, peracetic acid, ozone and UV radiation.

    Science.gov (United States)

    da Costa, Juliana Berninger; Rodgher, Suzelei; Daniel, Luiz Antonio; Espíndola, Evaldo Luiz Gaeta

    2014-11-01

    The toxic potential of four disinfectant agents (chlorine, ozone, peracetic acid and UV radiation), used in the disinfection of urban wastewater, was evaluated with respect to four aquatic organisms. Disinfection assays were carried out with wastewater from the city of Araraquara (São Paulo State, Brazil), and subsequently, toxicity bioassays were applied in order to verify possible adverse effects to the cladocerans (Ceriodaphnia silvestrii and Daphnia similis), midge larvae Chironomus xanthus and fish (Danio rerio). Under the experimental conditions tested, all the disinfectants were capable of producing harmful effects on the test organisms, except for C. xanthus. The toxicity of the effluent to C. silvestrii was observed to increase significantly as a result of disinfection using 2.5 mg L(-1) chlorine and 29.9 mg L(-1) ozone. Ozonation and chlorination significantly affected the survival of D. similis and D. rerio, causing mortality of 60 to 100 % in comparison to the non-disinfected effluent. In experiments with effluent treated with peracetic acid (PAA) and UV radiation, a statistically significant decrease in survival was only detected for D. rerio. This investigation suggested that the study of the ideal concentrations of disinfectants is a research need for ecologically safe options for the treatment of wastewater.

  12. Toxicity on aquatic organisms exposed to secondary effluent disinfected with chlorine, peracetic acid, ozone and UV radiation.

    Science.gov (United States)

    da Costa, Juliana Berninger; Rodgher, Suzelei; Daniel, Luiz Antonio; Espíndola, Evaldo Luiz Gaeta

    2014-11-01

    The toxic potential of four disinfectant agents (chlorine, ozone, peracetic acid and UV radiation), used in the disinfection of urban wastewater, was evaluated with respect to four aquatic organisms. Disinfection assays were carried out with wastewater from the city of Araraquara (São Paulo State, Brazil), and subsequently, toxicity bioassays were applied in order to verify possible adverse effects to the cladocerans (Ceriodaphnia silvestrii and Daphnia similis), midge larvae Chironomus xanthus and fish (Danio rerio). Under the experimental conditions tested, all the disinfectants were capable of producing harmful effects on the test organisms, except for C. xanthus. The toxicity of the effluent to C. silvestrii was observed to increase significantly as a result of disinfection using 2.5 mg L(-1) chlorine and 29.9 mg L(-1) ozone. Ozonation and chlorination significantly affected the survival of D. similis and D. rerio, causing mortality of 60 to 100 % in comparison to the non-disinfected effluent. In experiments with effluent treated with peracetic acid (PAA) and UV radiation, a statistically significant decrease in survival was only detected for D. rerio. This investigation suggested that the study of the ideal concentrations of disinfectants is a research need for ecologically safe options for the treatment of wastewater. PMID:25213288

  13. Trends of chlorinated organic contaminants in Great Lakes trout and walleye from 1970-1998

    Science.gov (United States)

    Hickey, J.P.; Batterman, S.A.; Chernyak, S.M.

    2006-01-01

    Levels of chlorinated organic contaminants in predator fish have been monitored annually in each of the Great Lakes since the 1970s. This article updates earlier reports with data from 1991 to 1998 for lake trout (Salvelinus namaycush) and (Lake Erie only) walleye (Sander vitreus) to provide a record that now extends nearly 30 years. Whole fish were analyzed for a number of industrial contaminants and pesticides, including polychlorinated biphenyls (PCBs), dichloro-diphenyl-trichloroethane (DDT), dieldrin, toxaphene, and mirex, and contaminant trends were quantified using multicompartment models. As in the past, fish from Lakes Michigan, Ontario, and Huron have the highest levels of PCBs, DDT, and dieldrin; Superior has the highest levels of toxaphene; and Ontario has the highest levels of mirex. In the period after curtailment of chemical use, concentrations rapidly decreased, represented by relatively short half-lives from approximately 1 to 9 years. Although trends depend on both the contaminant and the lake, in many cases the rate of decline has been decreasing, and concentrations are gradually approaching an irreducible concentration. For dioxin-like PCBs, levels have not been decreasing during the most recent 5-year period (1994 to 1998). In some cases, the year-to-year variation in contaminant levels is large, mainly because of food-web dynamics. Although this variation sometimes obscures long-term trends, the general pattern of a rapid decrease followed by slowing or leveling-off of the downward trend seems consistent across the Great Lakes, and future improvements of the magnitude seen in the 1970s and early 1980s likely will take much longer.

  14. Spectrophotometric determination of the acidity constants of calcon in water and mixed water–organic solvents

    Directory of Open Access Journals (Sweden)

    MOHAMMAD MAZLOUM-ARDAKANI

    2009-02-01

    Full Text Available The acid–base properties of calcon (1-(2-hydroxy-1-naphthylazo-2-naphthol-4-sulfonic acid in water and mixed water–organic solvents at 25 °C at an ionic strength of 0.10 M are studied by a multiwavelength spectrophotometric method. The organic solvents used were the amphiprotic (methanol, dipolar aprotic (dimethylsulfoxide, and low basic aprotic (acetonitrile. To evaluate the pH absorbance data, a resolution method based on the combination of soft- and hard-modeling was applied. The acidity constants of all related equilibria were estimated using the whole spectral fitting of the collected data to an established factor analysis model. The data analysis program Datan was applied for determination of the acidity constants. The corresponding pKa values were determined in water and mixed water–organic solvents. Linear relationship between the acidity constants and the mole fraction of the different sol-vents in the mixtures exist. The effect of solvent properties on acid–base behavior is discussed.

  15. QSAR studies of the dispersion of SWNTs in different organic solvents

    Energy Technology Data Exchange (ETDEWEB)

    Salahinejad, M., E-mail: salahinejad@gmail.com [NSTRI, Environmental Laboratory (Iran, Islamic Republic of); Zolfonoun, E. [NSTRI, Waste Management Department (Iran, Islamic Republic of)

    2013-11-15

    Artificial neural network (ANN) and multiple linear regression (MLR) approaches were successfully applied to construct quantitative structure–activity relationship models of the dispersibility of single-walled carbon nanotubes (SWNTs) in different organic solvents. A subset of the calculated descriptors selected by enhanced replacement method (ERM) was used in the QSPR models development. The predictive abilities of ERM–MLR and ERM–ANN models were determined using a test set of six organic solvents affording predictive correlation coefficients of 0.924 and 0.963, respectively, showing good predictive power of the models obtained. The final models satisfied a set of rigorous validation criteria and performed well in predicting of the external test set. The results obtained in this study, confirm the importance of steric and electrostatic interactions, molecular flexibility, polarizability and hydrogen bonding ability of organic solvents in SWNTs dispersibility. This information could be useful for identification of some key molecular features of solvent molecules and to find the proper solvent for SWNTs dispersion.

  16. Formation of emerging DBPs from the chlorination and chloramination of seawater algal organic matter and related model compounds

    KAUST Repository

    Nihemaiti, Maolida

    2014-05-01

    Limited studies focused on reactions occurring during disinfection and oxidation processes of seawater. The aim of this work was to investigate disinfection by-products (DBPs) formation from the chlorination and chloramination of seawater algal organic matter and related model compounds. Simulated algal blooms directly growing in Red Sea, red tide samples collected during an algal bloom event and Hymenomonas sp. monoculture were studied as algal organic matter sources. Experiments were conducted in synthetic seawater containing bromide ion. A variety of DBPs was formed from the chlorination and chloramination of algal organic matter. Brominated DBPs (bromoform, DBAA, DBAN and DBAcAm) were the dominant species. Iodinated DBPs (CIAcAm and iodinated THMs) were detected, which are known to be highly toxic compared to their chlorinated or brominated analogues. Algal organic matter was found to incorporate important precursors of nitrogenous DBPs (N-DBPs), which have been reported to be more toxic than regulated THMs and HAAs. Isotopically-labeled monochloramine (15N- NH2Cl) was used in order to investigate the nitrogen source in N-DBPs. High formation of N-DBPs was found from Hymenomonas sp. sample in exponential growth phase, which was enriched in nitrogen-containing organic compounds. High inorganic nitrogen incorporation was found from the algal samples enriched in humic-like compounds. HAcAms formation was studied from chlorination and chloramination of amino acids. Asparagine, aspartic acid and other amino acids with an aromatic structure were found to be important precursors of HAcAms and DCAN. Factors affecting HAcAms formation (Cl2/ amino acid molar ratio and pH) were evaluated. Studies on the formation kinetics of DCAcAm and DCAN from asparagine suggested a rapid formation of DCAcAm from organic nitrogen (amide group) and a slower incorporation of inorganic nitrogen coming from monochloramine to form DCAN. High amounts of DCAN and DCAcAm were detected from the

  17. Organic aqueous tunable solvents (OATS): a vehicle for coupling reactions and separations.

    Science.gov (United States)

    Pollet, Pamela; Hart, Ryan J; Eckert, Charles A; Liotta, Charles L

    2010-09-21

    In laboratory-based chemical synthesis, the choice of the solvent and the means of product purification are rarely determined by cost or environmental impact considerations. When a reaction is scaled up for industrial applications, however, these choices are critical: the separation of product from the solvent, starting materials, and byproduct usually constitutes 60-80% of the overall cost of a process. In response, researchers have developed solvents and solvent-handling methods to optimize both the reaction and the subsequent separation steps on the manufacturing scale. These include "switchable" solvents, which are designed so that their physical properties can be changed abruptly, as well as "tunable" solvents, wherein the solvent's properties change continuously through the application of an external stimulus. In this Account, we describe the organic aqueous tunable solvent (OATS) system, examining two instructive and successful areas of application of OATS as well as its clear potential for further refinement. OATS systems address the limitations of biphasic processes by optimizing reactions and separations simultaneously. The reaction is performed homogeneously in a miscible aqueous-organic solvent mixture, such as water-tetrahydrofuran (THF). The efficient product separation is conducted heterogeneously by the simple addition of modest pressures of CO(2) (50-60 bar) to the system. Under these conditions, the water-THF phase splits into two relatively immiscible phases: the organic THF phase contains the hydrophobic product, and the aqueous phase contains the hydrophilic catalyst. We take advantage of the unique properties of OATS to develop environmentally benign and cost-competitive processes relevant in industrial applications. Specifically, we describe the use of OATS for optimizing the reaction, separation, design, and recycling of (i) Rh-catalyzed hydroformylation of olefins such as 1-octene and (ii) enzyme-catalyzed hydrolysis of 2-phenylacetate. We

  18. Prioritizing substitution of organic solvents in industrial cleaning processes

    DEFF Research Database (Denmark)

    Rasmussen, Pia Brunn; Jacobsen, Thomas

    1997-01-01

    A method for prioritizing the substitution of volatile organic compounds (VOC) used in industrial cleaning processes is developed. The result is a matrix, which, if all information can be obtained, gives a comprehensive description of the effects, exposure and emission of VOC, as well...... as the prospects for performing the substitution with a vegetable ester. It can be a tool for companies to decide which cleaning process has the highest demand for substitution, if there is a choice between several processes, but it may also be a tool to convince companies to use non-volatile, low-toxic cleaning...

  19. Effect of chlorination and ozone pre-oxidation on the photobacteria acute toxicity for dissolved organic matter from sewage treatment plants

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    The effect of chlorination and ozone pre-oxidation on the photobacteria acute toxicity for dissolved organic matter(DOM) from sewage treatment plants was investigated in this study.The results show that ozone pre-oxidation enhanced the photobacteria acute toxicity of the water samples.DOM before and after ozone pre-oxidation was fractionated by resins into six kinds of hydrophobic and hydrophilic organics.The six fractions were chlorinated individually and the photobacteria acute toxicity before and after chlorination was tested.It was found that the percentage of hydrophilic organics in DOM significantly increased after ozone pre-oxidation and hydrophilic organics exhibited remarkably higher acute toxicity than hydrophobic organics.In view of potentiometric titration and fourier transform infrared(FTIR) analysis,the hydrophilic organics showed a rather higher content of ph-OH structures than hydrophobic organics.

  20. Psychophysical Evaluation of Achromatic and Chromatic Vision of Workers Chronically Exposed to Organic Solvents

    International Nuclear Information System (INIS)

    The purpose of this paper was to evaluate achromatic and chromatic vision of workers chronically exposed to organic solvents through psychophysical methods. Thirty-one gas station workers (31.5 ± 8.4 years old) were evaluated. Psychophysical tests were achromatic tests (Snellen chart, spatial and temporal contrast sensitivity, and visual perimetry) and chromatic tests (Ishihara's test, color discrimination ellipses, and Farnsworth-Munsell 100 hue test FM100). Spatial contrast sensitivities of exposed workers were lower than the control at spatial frequencies of 20 and 30 cpd whilst the temporal contrast sensitivity was preserved. Visual field losses were found in 10-30 degrees of eccentricity in the solvent exposed workers. The exposed workers group had higher error values of FM100 and wider color discrimination ellipses area compared to the controls. Workers occupationally exposed to organic solvents had abnormal visual functions, mainly color vision losses and visual field constriction

  1. Psychophysical Evaluation of Achromatic and Chromatic Vision of Workers Chronically Exposed to Organic Solvents

    Directory of Open Access Journals (Sweden)

    Eliza Maria da Costa Brito Lacerda

    2012-01-01

    Full Text Available The purpose of this paper was to evaluate achromatic and chromatic vision of workers chronically exposed to organic solvents through psychophysical methods. Thirty-one gas station workers (31.5 ± 8.4 years old were evaluated. Psychophysical tests were achromatic tests (Snellen chart, spatial and temporal contrast sensitivity, and visual perimetry and chromatic tests (Ishihara's test, color discrimination ellipses, and Farnsworth-Munsell 100 hue test—FM100. Spatial contrast sensitivities of exposed workers were lower than the control at spatial frequencies of 20 and 30 cpd whilst the temporal contrast sensitivity was preserved. Visual field losses were found in 10–30 degrees of eccentricity in the solvent exposed workers. The exposed workers group had higher error values of FM100 and wider color discrimination ellipses area compared to the controls. Workers occupationally exposed to organic solvents had abnormal visual functions, mainly color vision losses and visual field constriction.

  2. A simple method for determining water content in organic solvents based on cobalt(II) complexes

    Institute of Scientific and Technical Information of China (English)

    Lin Zhou; Xiao Hua Liu; Hai Xin Bai; Hong Juan Wang

    2011-01-01

    A method to determine water content in organic solvents was developed based on the color change of cobalt(II) nitrate in different solvents. The color-change mechanism and optimal conditions for determining the water content were investigated. The results showed that there was a good linear relationships between the absorbance of cobalt(II) complexes in organic solvents and water contents with y in 0.9989~0.9994. This method has the advantages of low cost, good reproducibility, good sensitivity, simple in operation, fast in detection, friendly to the environment and no limitation on linear range for determining water content. It was used to determine water in samples with a satisfactory recovery in 97.81%~101.24%.

  3. Separation of Acetic Acid from Aqueous Solution using Various Organic Solvents

    Directory of Open Access Journals (Sweden)

    Md. Zaved Hossain Khan

    2014-01-01

    Full Text Available 800x600 Normal 0 false false false EN-US X-NONE X-NONE MicrosoftInternetExplorer4 In the study a model has been developed to separate the acetic acid from aqueous solution by liquid-liquid extraction and find out the proper solvent for this separation. Various solvents such as n-butanol, iso butanol, amyl alcohol and ethyl acetate are used for separation of acetic acid from water. The binodal curves (mutual solubility curves for acetic acid distributed between water and an organic solvent were obtained by titrating known mixtures of two components (water and solvents with the third component acetic acid to the point of first appearance of permanent turbidity. In order to determine the tie-lines, the absorbance of the coexisting phases, obtained by the separation of ternary mixtures within the binodal curve are needed to be determined. The absorbance of each point had been determined by a UV spectrophotometer. Distribution diagrams are obtained by plotting weight percent of acetic acid in solvent phase against the weight percent of acetic acid in water phase. Selectivity diagrams are also obtained by plotting (wt. % of acetic acid / (percent of acetic acid + percent of water in solvent phase against the same quantity in the diluent phase. The separation factor is determined numerically from the tie-line data.

  4. Solubilities of p-coumaric and caffeic acid in ionic liquids and organic solvents

    International Nuclear Information System (INIS)

    Highlights: ► New solubility data of p-coumaric and caffeic acid in ionic liquids and organic solvents. ► Normal melting point temperature and enthalpy of fusion of p-coumaric and caffeic acid. ► Thermogravimetric analysis for p-coumaric and caffeic acid. ► Correlation with UNIQUAC and NRTL. -- Abstract: The solubilities of two cinnamic acid derivatives, namely p-coumaric acid and caffeic acid, in six 1-alkyl-3-methyl imidazolium based ionic liquids composed of the PF6−, BF4−, TFO− and TF2N− anions, and in two organic solvents, t-pentanol and ethyl acetate, have been measured at the temperature range of about (303 to 317) K. The p-coumaric acid was found to be more soluble than caffeic acid in all studied solvents. Higher solubilities of both acids were observed in the ionic liquids composed of the BF4− and TFO− anions. The increase of the alkyl chain length on the cation invokes a decrease in solubility in the case of hydrophilic ionic liquids composed of BF4− anion, while in the case of hydrophobic ones composed of PF6− anion an increase in the solubility is observed. Between the two organic solvents t-pentanol is better solvent than ethyl acetate for both acids. Moreover, using the van’t Hoff equations the apparent Gibbs energy, enthalpy, and entropy of solution were calculated. Finally, successful correlation of the experimental data was achieved with the UNIQUAC and the NRTL activity coefficient models, while poor predictions of the solubility of the two acids in the organic solvents were obtained with two UNIFAC models

  5. Polyethylene as a source of artifacts in the paper chromatography of chlorinated hydrocarbon insecticides

    Science.gov (United States)

    Van Valin, C.C.; Kallman, B.J.; O'Donnell, J.J

    1963-01-01

    The introduction of artifacts from vessels, materials, and chemicals is a serious problem in the study of pesticide residues. It is therefore of interest to record findings that polyethylene wash bottles contain substances soluble in organic solvents and reactive with the silver nitrate chromogenic spray commonly employed in the paper chromatographic analysis of chlorinated organic insecticides.

  6. Random mutagenesis and selection of organic solvent-stable haloperoxidase from Streptomyces aureofaciens.

    Science.gov (United States)

    Yamada, Ryosuke; Higo, Tatsutoshi; Yoshikawa, Chisa; China, Hideyasu; Yasuda, Masahiro; Ogino, Hiroyasu

    2015-01-01

    Haloperoxidases are useful oxygenases involved in halogenation of a range of water-insoluble organic compounds and can be used without additional high-cost cofactors. In particular, organic solvent-stable haloperoxidases are desirable for enzymatic halogenations in the presence of organic solvents. In this study, we adopted a directed evolution approach by error-prone polymerase chain reaction to improve the organic solvent-stability of the homodimeric BPO-A1 haloperoxidase from Streptomyces aureofaciens. Among 1,000 mutant BPO-A1 haloperoxidases, an organic solvent-stable mutant OST48 with P123L and P241A mutations and a high active mutant OST959 with H53Y and G162R mutations were selected. The residual activity of mutant OST48 after incubation in 40% (v/v) 1-propanol for 1 h was 1.8-fold higher than that of wild-type BPO-A1. In addition, the OST48 mutant showed higher stability in methanol, ethanol, dimethyl sulfoxide, and N,N-dimethylformamide than wild-type BPO-A1 haloperoxidase. Moreover, after incubation at 80°C for 1 h, the residual activity of mutant OST959 was 4.6-fold higher than that of wild-type BPO-A1. Based on the evaluation of single amino acid-substituted mutant models, stabilization of the hydrophobic core derived from P123L mutation and increased numbers of hydrogen bonds derived from G162R mutation led to higher organic solvent-stability and thermostability, respectively.

  7. Chemical aspects of incinerating highly chlorinated and actinide α contaminated organic waste: application to the Iris process

    International Nuclear Information System (INIS)

    A fraction of the waste produced by nuclear activities is combustible, and thus suitable for incineration to produce gases, ash and fines. A typical composition representative of actual organic waste mixtures was defined for the purpose of investigating possible heat treatment processes; the composition is identified according to components Table 1 and elements Table II. The high polyvinyl chloride (PVC) content is responsible for the high chlorine potential in the process equipment. The quantity and quality of the resulting solid residue depends entirely on the inorganic load of the organic waste, whose behavior is entirely conditioned by the process conditions. For example, pure polyethylene is totally converted to gases (water and carbon dioxide), while the composition shown in Table II produces a range of oxides and chlorides. The high chlorine content results in partial chlorination of the inorganic compounds, but can also lead to interactions with the process equipment. The temperature dependent variation of the chlorination equilibrium constants of various metals clearly shows that all the elements of technological alloys may be subject to active corrosion by hydrochloric acid. However, the corresponding oxides-notably alumina-are much less sensitive to corrosion; aluminum-based alloys are therefore preferred for incinerator construction and to limit corrosion by hydrochloric acid. Thermodynamic and kinetic studies led to the development of the IRIS three-step process. Gas emissions occurring during processing of solid materials are completely oxidized in the after-burning step at 1100 deg C, and are then ducted to a HERA filtration system capable of retaining all the actinide α radionuclides. Although corrosion-related problems are attenuated in the two-step process chlorine can combine with the inorganic waste material to form chlorides with potentially damaging effects on the system; this is the case for zinc chloride and for volatile chlorides in

  8. Differential behaviour of four plant polysaccharide synthases in the presence of organic solvents.

    Science.gov (United States)

    Kerry, M E; Gregory, A C; Bolwell, G P

    2001-08-01

    The behaviour of four membrane-bound glycosyl transferases involved in cell wall polysaccharide synthesis has been studied in relation to the effects of a graded series of organic solvents on their activity and type of product formed. Relative enzyme inhibition observed for some solvents was in direct relationship to the hydrophilicity of the product. This was in the order of arabinan synthase > callose synthase> xylan synthase > beta-1,4-glucan synthase. The former two were always inhibited, the xylan synthase rather less so. However, the beta-1,4-glucan synthase showed significant increases in substrate incorporation in the presence of solvents. A graded series of primary alcohols were much more effective in enhancing activity than acetone, ethyl acetate and dimethyl formamide. In the presence of the most effective solvent, methanol, there was considerable activation of beta-1,4-glucan production. This reciprocal nature of the behaviour of the beta-1,4- and beta-1,3-glucan synthases in organic solvent is supportive of recent molecular data that the two types of glucans are catalysed by separate enzyme systems. However, the results reported here do not totally negate the proposition that either enzyme is capable of synthesising the other linkage in minor amounts in vitro. PMID:11430978

  9. Chemo-enzymatic peptide synthesis and derivatisation using Subtilisin A in anhydrous organic solvents

    NARCIS (Netherlands)

    Nuijens, T.

    2012-01-01

    In this thesis it is demonstrated that Alcalase and Cal-B in neat organic solvent can perform unique and cost-efficient conversions that are useful in the peptide area. Not only can Alcalase be used to prepare several C-terminally derivatized amino acids and peptides (such as amides, esters and aryl

  10. Organic solvents induce the formation of oil-in-ionic liquid microemulsion aggregations.

    Science.gov (United States)

    Gao, Yanan; Li, Na; Zhang, Shaohua; Zheng, Liqiang; Li, Xinwei; Dong, Bin; Yu, Li

    2009-02-01

    The role of four organic solvents in the formation process of 1-butyl-3-methylimidazolium tetrafluoroborate (bmimBF4) based ionic liquid (IL) microemulsions is investigated. The results showed that the addition of Triton X-100 remarkably decreased the conductivity of bmimBF4. The added organic solvents provided a strong apolar environment for the hydrophobic tails of Triton X-100 and caused the surfactant molecules to aggregate into the interfacial film of oil-in-bmimBF4 (O/IL) microemulsions. As a result, the conductivities of the solutions were initially increased because the insulative Triton X-100 molecules were assembled, which corresponded to increasing the concentration of continuous bmimBF4 solutions. The hydrophobic interaction between the dispersed organic solvents and the hydrophobic tails of Triton X-100 may be the driving force for the formation of O/IL microemulsions. The droplets of O/IL microemulsions were successively swollen by organic solvents, and a bicontinuous IL-containing microemulsion was observed by freeze-fracture transmission electron microscopy for the first time. The current study can help in further understanding the ILs-containing microemulsions and thereby improve microemulsion theory. PMID:19138136

  11. Preparation of PLA and PLGA nanoparticles by binary organic solvent diffusion method

    Institute of Scientific and Technical Information of China (English)

    蒋新宇; 周春山; 唐课文

    2003-01-01

    The nanoparticles of polylactide (PLA) and poly(lactide-co-glycolide) (PLGA) were prepared by the bi-nary organic solvent diffusion method. The yield, particle size and size distribution of these nanoparticles wereevaluated. The yield of nanoparticles prepared by this method is over 90%, and the average size of the nanoparticlesis between 130-180 nm. In order to clarify the effect of the organic solvent used in the system on nanoparticle yieldand size, the cloud points of PLA and PLGA were examined by cloud point titration. The results indicate that theyields of nanoparticles increase with the increase of ethanol in the acetone solution and attain the maximum at thecloud point of ethanol, while the size of nanoparticles decreases with the increase of ethanol in the acetone solutionand attains the minimum at the cloud point of ethanol. The optimal composition ratio of binary organic solvents coin-cides to that near the cloud point and the optimal condition of binary organic solvents can be predicted.

  12. Aggregation behavior of cholic acid derivatives in organic solvents and in water

    NARCIS (Netherlands)

    Willemen, H.M.

    2002-01-01

    In this thesis various cholic acid derivatives are reported that display aggregation in water or in organic solvents. Spontaneous aggregation of single molecules into larger, ordered structures occurs at the borderline of solubility. Amphiphilic compounds, or surfactants, which possess a hydrophobic

  13. Elucidation of the mechanism of chiral selectivity in diastereomeric salt formation using organic solvent nanofiltration.

    Science.gov (United States)

    Ghazali, Nazlee F; Patterson, Darrell A; Livingston, Andrew G

    2004-04-21

    Organic solvent nanofiltration (OSN) was used to investigate the mechanism of chiral selectivity in diastereomeric salt formation of alpha-phenylethylamine with D-tartaric acid and di-p-toluoyl-D-tartaric acid as resolving agents; results indicate that for these systems chiral selectivity occurs only upon crystallisation and chiral interactions in solution were negligible. PMID:15069495

  14. Remediation of soils, sediments and sludges by extraction with organic solvents

    NARCIS (Netherlands)

    Noordkamp, E.

    1999-01-01

    Remediation of contaminated soils, sediments and sludges by extraction with organic solvents is still in the initial stages of development. So far hardly any scientific research has been carried out into this approach. Therefore, the main objective of the present investigation was to study the effec

  15. Cochlear condition and olivocochlear system of gas station attendants exposed to organic solvents

    Directory of Open Access Journals (Sweden)

    Tochetto, Tania Maria

    2012-01-01

    Full Text Available Introduction: Organic solvents have been increasingly studied due to its ototoxic action. Objective: Evaluate the conditions of outer hair cells and olivocochlear system in individuals exposed to organic solvents. Method: This is a prospective study. 78 gas station attendants exposed to organic solvents had been evaluated from three gas stations from Santa Maria city, Rio Grande do Sul (RS. After applying the inclusion criteria, the sample was constituted by 24 individuals. The procedures used on the evaluation were audiological anamnesis, Transient otoacoustic emissions (TEOAES and research for the suppressive effect of TEOAES. A group control (GC compounded by 23 individuals was compared to individuals exposed and non-exposed individuals. The data collection has been done in the room of Speech Therapy of Workers Health Reference Center of Santa Maria. Results: The TEOAES presence was major in the left ear in both groups; the average relation of TEOAES signal/noise in both ears was greater in GE; the TEOAES suppressive effect in the right ear was higher in the individual of GE (62,5% and in the left ear was superior in GC (86,96%, with statistically significant difference. The median sign/noise ratio of TEOAES, according to the frequency range, it was higher in GC in three frequencies ranges in the right ear and one in the left ear. Conclusion: It was not found signs of alteration on the outer hair cells neither on the olivocochlear medial system in the individuals exposed to organic solvents.

  16. Exceptional thermal stability and organic solvent tolerance of an esterase expressed from a thermophilic host

    DEFF Research Database (Denmark)

    Mei, Yuxia; Peng, Nan; Zhao, Shumiao;

    2012-01-01

    exclusively in solution, whereas EcSisEstA appeared solely as monomer. The former exhibited a stronger resistance to organic solvents than the latter in general, having a much higher temperature optimum (90°C vs. 65°C). More strikingly, SisEstA exhibited a half-life that was more than 32-fold longer than...

  17. Understanding mechanisms of asphaltene adsorption from organic solvent on mica.

    Science.gov (United States)

    Natarajan, Anand; Kuznicki, Natalie; Harbottle, David; Masliyah, Jacob; Zeng, Hongbo; Xu, Zhenghe

    2014-08-12

    The adsorption process of asphaltene onto molecularly smooth mica surfaces from toluene solutions of various concentrations (0.01-1 wt %) was studied using a surface forces apparatus (SFA). Adsorption of asphaltenes onto mica was found to be highly dependent on adsorption time and asphaltene concentration of the solution. The adsorption of asphaltenes led to an attractive bridging force between the mica surfaces in asphaltene solution. The adsorption process was identified as being controlled by the diffusion of asphaltenes from the bulk solution to the mica surface with a diffusion coefficient on the order of 10(-10) m(2)/s at room temperature, depending on the asphaltene bulk concentration. This diffusion coefficient corresponds to a hydrodynamic molecular radius of approximately 0.5 nm, indicating that asphaltene diffuses to mica surfaces as individual molecules at very low concentration (e.g., 0.01 wt %). Atomic force microscopy images of the adsorbed asphaltenes on mica support the results of the SFA force measurements. The results from the SFA force measurements provide valuable insights into the molecular interactions (e.g., steric repulsion and bridging attraction as a function of distance) of asphaltenes in organic media and hence their roles in crude oil and bitumen production.

  18. Effect of Mixed Solvents Consisting of Water and Organic Solvent on Preparation of Medium-Responsive Grafted Cellulose Film by Means of Photografting

    Directory of Open Access Journals (Sweden)

    Irwan Ginting-Suka

    2006-11-01

    Full Text Available Cellulose having a medium-responsive function were synthesized by photografting of methacrylic acid (MAA on regenerated cellulose film (thickness = 20 µm at 60°C using mixed solvent consisting of water and organic solvents such as acetone and methanol. Xanthone was used as photoinitiator by coating on the film surfaces. A maximum percentage of grafting was observed at a certain concentration of organic solvent. MAA-grafted cellulose films produced showing homogeneous distribution of grafted chains, which was examined by scanning electron microscopy. The modified films also exhibit medium responsive character, it shrinks in acidic and swells in basic solution. Moreover, the grafted film exhibited the ability to absorb copper ion, which was not influenced by the solvent used in grafting processes.

  19. Formation of chlorinated organic compounds in fluidized bed combustion of recycled fuels

    International Nuclear Information System (INIS)

    Four tests of co-combustion of recycled fuels (REP) with peat and coal in the 15 kW fluidized bed reactor were performed. The recycled fuel was so-called dry fraction in four vessels sampling at Keltinmaeki. In three tests a part of peat energy was replaced with coal. The mixtures were prepared so that in all mixtures 25 % of energy was recycled fuel and 75 % was either peat or the mixture of peat and coal. The concentrations of polyaromatic hydrocarbons (PAH), polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs) and chlorophenols decreased with increasing part of coal due to the increasing sulphur/chlorine ratio. Principal Component Analysis (PCA) and Partial Least Square regression analysis (PLS) showed that the chlorine, copper and sulphur contents of the fuel effected most on the concentrations of chlorophenols, chlorobenzenes, PCBs and PCDDs/PCDFs. Other variables influencing on a model were the lead concentration and the sulphur/chlorine ratio in fuel and the hydrogen chloride concentration of the flue gas. The concentrations of chlorophenols and chlorobenzenes were also significant for PCDD/PCDF concentrations in flue gas. The sulphur, chlorine, copper and chromium contents in fly ash and the temperature of the reactor influenced on the chlorophenol, chlorobenzene, PCB and PCDD/PCDF concentrations in fly ash. The chlorophenol and chlorobenzene contents in fly ash, the sulphur/chlorine ratio and the lead content in fuel, the sulphur dioxide, hydrogen chloride and carbon monoxide concentrations in flue gas had also influence on PCDD/PCDF concentrations in fly ash

  20. Covalent modification of graphite oxide with acetic anhydride to enhance dispersibility in organic solvents

    Science.gov (United States)

    Li, Jingjing; Yang, Anwei; Zhang, Chen; Zhang, Lei; Sun, Feifei; Ma, Ning

    2016-05-01

    Graphite oxide (GO) was modified by acetic anhydride via a catalyzed ring-opening reaction of the attached epoxy groups at very mild condition. The dispersion of the modified GO is thus largely imporved in many organic solvents and the highest GO concentration reaches 2.0mg/mL in alkyl(aryl) chlorides, ethers, alcohols and cyclohexane, which is amongst the highest value for GO in organics.

  1. Natural attenuation of chlorinated volatile organic compounds in a freshwater tidal wetland: Field evidence of anaerobic biodegradation

    Science.gov (United States)

    Lorah, M.M.; Olsen, L.D.

    1999-01-01

    Field evidence collected along two groundwater flow paths shows that anaerobic biodegradation naturally attenuates a plume of chlorinated volatile organic compounds as it discharges from an aerobic sand aquifer through wetland sediments. A decrease in concentrations of two parent contaminants, trichloroethylene (TCE) and 1,1,2,2-tetrachloroethane (PCA), and a concomitant increase in concentrations of anaerobic daughter products occurs along upward flow paths through the Wetland sediments. The daughter products 1,2-dichloroethylene, vinyl chloride, 1,1,2-trichloroethane, and 1,2-dichloroethane are produced from hydrogenolysis of TCE and from PCA degradation through hydrogenolysis and dichloroelimination (reductive dechlorination) pathways. Total concentrations of TCE, PCA, and their degradation products, however, decrease to below detection levels within 0.15-0.30 m of land surface. The enhanced reductive dechlorination of TCE and PCA in the wetland sediments is associated with the naturally higher concentrations of dissolved organic carbon and the lower redox state of the groundwater compared to the aquifer. This field study indicates that wetlands and similar organic-rich environments at groundwater/surface-water interfaces may be important in intercepting groundwater contaminated with chlorinated organics and in naturally reducing concentrations and toxicity before sensitive surface-water receptors are reached.

  2. Morphology versus Vertical Phase Segregation in Solvent Annealed Small Molecule Bulk Heterojunction Organic Solar Cells

    Directory of Open Access Journals (Sweden)

    Alexander Kovalenko

    2015-01-01

    Full Text Available The deep study of solvent annealed small molecules bulk heterojunction organic solar cells based on DPP(TBFu2 : PC60BM blend is carried out. To reveal the reason of the solvent annealing advantage over the thermal one, capacitance-voltage measurements were applied. It was found that controlling the vertical phase segregation in the solar cells a high fullerene population in the vicinity of the cathode could be achieved. This results in increase of the shunt resistance of the cell, thus improving the light harvesting efficiency.

  3. Effect of organic solvent properties on enthalpies of their mixing with uranyl nitrate

    International Nuclear Information System (INIS)

    Results of studying dissolution enthalpies of anhydrons uranyl nitrate and its hexahydrate in different organic solvents and water are generalized. Analysis of different solvation effects during uranyl nitrate and its hexahydrate dissolution in 26 solvents shows that the main contribution to dissolution enthalpy is made by acidic-basic interaction of uranyl-nitrates with donor lone electron pairs. The obtained equations permit to predict with acceptable accuracy the values of dissolution enthalpies of the mentioned compounds in other midea on the basis of their physico-chemical properties

  4. A Systematic Study of the Dispersion of SWNTs in Organic Solvents

    OpenAIRE

    Cheng, Qiaohuan, (Thesis); Debnath, Sourabhi; O'Neill, Luke; Hedderman, Theresa; Gregan, Elizabeth, (Thesis); Byrne, Hugh

    2010-01-01

    Dispersions of as-produced HiPco single-walled carbon nanotubes (SWNTs) in a series of organic solvents were prepared by dilution with the aid of tip sonication. Mild centrifugation (~ 945 g) was carried out to remove large bundles. Atomic force microscopy (AFM) studies revealed that the bundle size decreased as the dispersion was diluted. By measuring the UV-vis-NIR absorption before and after centrifugation as a function of the concentration, the dispersion limit of SWNTs in each solvent ca...

  5. Breakpoint chlorination curves of greywater.

    Science.gov (United States)

    March, J G; Gual, M

    2007-08-01

    A study on chlorination of raw greywater with hypochlorite is reported in this paper. Samples were chlorinated in a variety of conditions, and residual chlorine (Cl2) was measured spectrophotometrically. For each sample, the chlorination curve (chlorine residuals versus chlorine dose) was obtained. Curves showed the typical hump-and-dip profile attributable to the formation and destruction of chloramines. It was observed that, after reactions with strong reductants and chloramines-forming compounds, the remaining organic matter exerted a certain demand of chlorine. The evolution of chlorination curves with addition of ammonia and dodecylbencene sulfonate sodium salt and with dilution of the greywater sample were studied. In addition, chlorination curves at several contact times have been obtained, resulting in slower chlorine decay in the hump zone than in the dip zone. In addition, the decay of coliforms in chlorinated samples was also investigated. It was found that, for a chlorination dosage corresponding to the maximum of the hump zone (average 8.9 mg Cl2/ L), samples were negative in coliforms after 10 to 30 minutes of contact time. After-growth was not observed within 3 days after chlorination. Implications in chlorination treatments of raw greywater can be derived from these results. PMID:17824528

  6. Improved Cellulose and Organic-Solvents based Lignocellulosic Fractionation Pre-treatment of Organic Waste for Bioethanol Production

    OpenAIRE

    Valeriy Bekmuradov; Grace Luk; Robin Luong

    2014-01-01

    This study investigates the performance of the Cellulose and Organic-Solvents based Lignocellulosic Fractionation (COSLIF) method for the pretreatment of Source-Separated Organic (SSO) waste. An improvement on the standard method of COSLIF pre-treatment was developed based on lower enzyme loading and using an ethanol washing instead of acetone. It was demonstrated that a much higher glucose yield (90% after 72 hours) was possible with this improvement, as compared to the original method, w...

  7. Determination of physical properties for the mixtures of [BMIM]Cl with different organic solvents

    Institute of Scientific and Technical Information of China (English)

    Hina Saba; Xinjun Zhu; Ye Chen; Yumei Zhang

    2015-01-01

    Physical properties including refractive index, density, viscosity and conductivity for binary mixtures of 1-butyl-3-methyl imidazolium chloride ([BMIM]Cl) and different organic solvents at 298.15 K have been investigated. Ex-cess molar volumes have been calculated and obtained data has been fitted by the Redlich–Kister equation. The density and refractive index were found to increase with increasing concentration of [BMIM]Cl, however, excep-tions do exist as in the case of dimethyl sulfoxide (DMSO)/[BMIM]Cl. For DMSO/[BMIM]Cl, the density decreases with increasing concentration. The addition of different organic solvents was able to disrupt the interactions within mixtures, leading to free mobility of ions. The free mobility of ions has been found to enhance conductivity and decrease viscosity to varying extents in al mixtures studied. It has been observed that solubility parameters, dielectric constants and composition of the solvents used play a vital role in determining the resultant properties. The data obtained wil play an important role in understanding the effect of the addition of organic solvents in ILs to enhance their applicability.

  8. Solvent dependence of Stokes shift for organic solute-solvent systems: A comparative study by spectroscopy and reference interaction-site model-self-consistent-field theory

    Science.gov (United States)

    Nishiyama, Katsura; Watanabe, Yasuhiro; Yoshida, Norio; Hirata, Fumio

    2013-09-01

    The Stokes shift magnitudes for coumarin 153 (C153) in 13 organic solvents with various polarities have been determined by means of steady-state spectroscopy and reference interaction-site model-self-consistent-field (RISM-SCF) theory. RISM-SCF calculations have reproduced experimental results fairly well, including individual solvent characteristics. It is empirically known that in some solvents, larger Stokes shift magnitudes are detected than anticipated on the basis of the solvent relative permittivity, ɛr. In practice, 1,4-dioxane (ɛr = 2.21) provides almost identical Stokes shift magnitudes to that of tetrahydrofuran (THF, ɛr = 7.58), for C153 and other typical organic solutes. In this work, RISM-SCF theory has been used to estimate the energetics of C153-solvent systems involved in the absorption and fluorescence processes. The Stokes shift magnitudes estimated by RISM-SCF theory are ˜5 kJ mol-1 (400 cm-1) less than those determined by spectroscopy; however, the results obtained are still adequate for dipole moment comparisons, in a qualitative sense. We have also calculated the solute-solvent site-site radial distributions by this theory. It is shown that solvation structures with respect to the C-O-C framework, which is common to dioxane and THF, in the near vicinity (˜0.4 nm) of specific solute sites can largely account for their similar Stokes shift magnitudes. In previous works, such solute-solvent short-range interactions have been explained in terms of the higher-order multipole moments of the solvents. Our present study shows that along with the short-range interactions that contribute most significantly to the energetics, long-range electrostatic interactions are also important. Such long-range interactions are effective up to 2 nm from the solute site, as in the case of a typical polar solvent, acetonitrile.

  9. Solvent dependence of Stokes shift for organic solute-solvent systems: A comparative study by spectroscopy and reference interaction-site model-self-consistent-field theory.

    Science.gov (United States)

    Nishiyama, Katsura; Watanabe, Yasuhiro; Yoshida, Norio; Hirata, Fumio

    2013-09-01

    The Stokes shift magnitudes for coumarin 153 (C153) in 13 organic solvents with various polarities have been determined by means of steady-state spectroscopy and reference interaction-site model-self-consistent-field (RISM-SCF) theory. RISM-SCF calculations have reproduced experimental results fairly well, including individual solvent characteristics. It is empirically known that in some solvents, larger Stokes shift magnitudes are detected than anticipated on the basis of the solvent relative permittivity, ɛr. In practice, 1,4-dioxane (ɛr = 2.21) provides almost identical Stokes shift magnitudes to that of tetrahydrofuran (THF, ɛr = 7.58), for C153 and other typical organic solutes. In this work, RISM-SCF theory has been used to estimate the energetics of C153-solvent systems involved in the absorption and fluorescence processes. The Stokes shift magnitudes estimated by RISM-SCF theory are ∼5 kJ mol(-1) (400 cm(-1)) less than those determined by spectroscopy; however, the results obtained are still adequate for dipole moment comparisons, in a qualitative sense. We have also calculated the solute-solvent site-site radial distributions by this theory. It is shown that solvation structures with respect to the C-O-C framework, which is common to dioxane and THF, in the near vicinity (∼0.4 nm) of specific solute sites can largely account for their similar Stokes shift magnitudes. In previous works, such solute-solvent short-range interactions have been explained in terms of the higher-order multipole moments of the solvents. Our present study shows that along with the short-range interactions that contribute most significantly to the energetics, long-range electrostatic interactions are also important. Such long-range interactions are effective up to 2 nm from the solute site, as in the case of a typical polar solvent, acetonitrile.

  10. Extraction of Betulin, Trimyristin, Eugenol and Carnosic Acid Using Water-Organic Solvent Mixtures

    Directory of Open Access Journals (Sweden)

    Fulgentius N. Lugemwa

    2012-08-01

    Full Text Available A solvent system consisting of ethyl acetate, ethyl alcohol and water, in the volume ratio of 4.5:4.5:1, was developed and used to extract, at room temperature, betulin from white birch bark and antioxidants from spices (rosemary, thyme, sage, and oregano and white oak chips. In addition, under reflux conditions, trimyristin was extracted from nutmeg using the same solvent system, and eugenol from olives was extracted using a mixture of salt water and ethyl acetate. The protocol demonstrates the use of water in organic solvents to extract natural products from plants. Measurement of the free-radical scavenging activity using by 2,2-diphenyl-1-picrylhydrazyl (DPPH indicated that the extraction of plant material using ethyl acetate, ethyl alcohol and water (4.5:4.5:1, v/v/v was exhaustive when carried out at room temperature for 96 h.

  11. Morphology and physiology of anaerobic granular sludge exposed to an organic solvent

    International Nuclear Information System (INIS)

    The use of quantitative image analysis techniques, together with physiological information might be used to monitor and detect operational problems in advance to reactor performance failure. Industrial organic solvents, such as White Spirit, are potentially harmful to granular sludge. In preliminary batch assays, 33 mg L-1 of solvent caused 50% relative biomass activity loss. In an expanded granular sludge blanket reactor fed with 40 mg L-1 of solvent, during 222 h, the reactor performance seemed to be unaffected, presenting COD removal efficiency consistently >95%. However, in the last days of exposure, the biogas production and the methane content were inhibited. Afterwards, already during recovery phase, the COD removal efficiency decreased to 33%, probably because the reactor was underloaded and the biomass became saturated in solvent only at this stage. In the first hours of exposure the specific acetoclastic and the specific hydrogenotrophic methanogenic activities decreased 29% and 21%, respectively. The % of aggregates projected area with equivalent diameter (Deq) > 1 mm decreased from 81% to 53%. The mean Deq of the aggregates ≥0.2 mm decreased, as well as the settling velocity, showing that the granules experienced fragmentation phenomenon caused by the solvent shock load. The ratio between total filaments length and total aggregates projected area (LfA) increased 2 days before effluent volatile suspended solids, suggesting that LfA could be an early-warning indicator of washout events.

  12. Transport and transformations of chlorinated-solvent contamination in a saprolite and fractured rock aquifer near a former wastewater-treatment plant, Greenville, South Carolina

    Science.gov (United States)

    Vroblesky, D.A.; Bradley, P.M.; Lane, J.W.; Robertson, J.F.

    1997-01-01

    The transport and fate of chlorinated-ethene contamination was investigated in a fractured-rock aquifer downgradient from a wastewater-treatment plant at a gas-turbine manufacturing facility inGreenville, South Carolina. A vapor-diffusion- sampler technique, developed for this investigation, located fracture zones that discharged contaminated ground water to surface water. The distribution ofchlorinated compounds and sulfate, comparison of borehole geophysical data, driller's logs, and the aquifer response to pumpage allowed subsurface contaminant-transport pathways to be delineated.The probable contaminant-transport pathway from the former aeration lagoon was southward. The probable pathway of contaminant transport from the former sludge lagoon was southward to and beneath Little Rocky Creek. South of the creek, the major pathway of contaminant transport appeared to be at a depth of approximately 80 to 107 feet below land surface. The contaminant-transport pathway from the former industrial lagoon was not readily discernible from existing data. A laboratory investigation, as well as examination of ground- water-chemistry data collected during this investigation and concentrations of chlorinated compounds collected during previous investigations,indicates that higher chlorinated compounds are being degraded to lower-chlorinated compounds in the contaminated aquifer. The approaches used in this investigation, as well as the findings, havepotential application to other fractured-rock aquifers contaminated by chlorinated ethenes.

  13. Efficient inverted organic light-emitting devices by amine-based solvent treatment (Presentation Recording)

    Science.gov (United States)

    Song, Myoung Hoon; Choi, Kyoung-Jin; Jung, Eui Dae

    2015-10-01

    The efficiency of inverted polymer light-emitting diodes (iPLEDs) were remarkably enhanced by introducing spontaneously formed ripple-shaped nanostructure of ZnO (ZnO-R) and amine-based polar solvent treatment using 2-methoxyethanol and ethanolamine (2-ME+EA) co-solvents on ZnO-R. The ripple-shape nanostructure of ZnO layer fabricated by solution process with optimal rate of annealing temperature improves the extraction of wave guide modes inside the device structure, and 2-ME+EA interlayer enhances the electron injection and hole blocking and reduces exciton quenching between polar solvent treated ZnO-R and emissive layer. As a result, our optimized iPLEDs show the luminous efficiency (LE) of 61.6 cd A-1, power efficiency (PE) of 19.4 lm W-1 and external quantum efficiency (EQE) of 17.8 %. This method provides a promising method, and opens new possibilities for not only organic light-emitting diodes (OLEDs) but also other organic optoelectronic devices such as organic photovoltaics, organic thin film transistors, and electrically driven organic diode laser.

  14. DETERMINATION OF CHLORINATED ORGANIC COMPOUNDS IN THE MAIN DRAINAGE CHANNEL OF KONYA

    OpenAIRE

    AYDIN, Mehmet Emin

    2000-01-01

    The main drainage channel of Konya collects drainage waters from farmlands of Konya and discharges to the salt lake. Since there is not any city municipal sewarage system in Konya sewage of the city also discharged to the main drainage channel. Along the channel, farmers use the channels water for irrigation purposes. Therefore a through examination of wastewater and determination of chlorinated compounds were necessary. In this research, analyses were carried by gas chromatography (GC) on wa...

  15. Changes in dissolved organic matter fluorescence and disinfection byproduct formation from UV and subsequent chlorination/chloramination

    Energy Technology Data Exchange (ETDEWEB)

    Lyon, Bonnie A.; Cory, Rose M.; Weinberg, Howard S., E-mail: howard_weinberg@unc.edu

    2014-01-15

    Highlights: • DBP formation from UV-chlorine/chloramine drinking water treatment was measured. • The effect of UV on DBP precursors was evaluated by fluorescence and PARAFAC. • UV alone decreased protein/tryptophan- and humic-like fluorescence. • Loss of two components correlated with cyanogen chloride formation (R{sup 2} = 0.79–0.91). • Loss of the components also correlated with chloral hydrate formation (R{sup 2} = 0.95–1.000). -- Abstract: Ultraviolet (UV) irradiation is being increasingly used to help drinking water utilities meet finished water quality regulations, but its influence on disinfection byproduct (DBP) precursors and DBP formation is not completely understood. This study investigated the effect of medium pressure (MP) UV combined with chlorination/chloramination on the fluorescent fraction of dissolved organic matter (DOM) isolated from a United States surface water with median total organic carbon content. Parallel factor analysis was used to understand how UV may alter the capacity of DOM to form DBPs of potential human health concern. The production of chloral hydrate and cyanogen chloride from MP UV followed by chlorine or chloramine, respectively, correlated with a decrease in fluorescence intensity of a protein/tryptophan-like component (R{sup 2} = 0.79–0.99) and a humic-like component (R{sup 2} = 0.91–1.00). This suggests that the UV-induced precursors to these compounds originated from DOM with similar characteristics to these components. The fluorescent DOM components identified in this study are similar to reoccurring components that have been previously identified in a range of raw and treated waters, and this work demonstrates the value of using fluorescence analysis of DOM to understand the relationships between DOM source and DBP formation under a range of treatment conditions.

  16. Relation between the interfacial tension in an organic solvent-water system and the parameters of the solvating capacity of the solvent

    International Nuclear Information System (INIS)

    It was shown that there is a linear relation between the empirical DE (diluent effect) and E/sub T/ parameters, which characterize the solvating capacity of the solvent, and the interfacial tension in an organic solvent-water two-phase system. Analysis of the sample correlation coefficients shows that the relation between the interfacial tension and the DE parameters of the solvents is closer to linear than the corresponding relation for the E/sub T/ parameters. During analysis of the data for 31 solvents it was established that the largest inverse correlation coefficient r = -0.98 is obtained with an equation of the DE = a + bσ/rho 1/3, type, were a and b are constants, and rho is the density of the solvent. The regression equation has the following form: DE = 7.586 - 0.147 σ/rho 1/3. Since the interfacial activity of hydrophobic surfactants decreases linearly with increase in the DE values, it follows from the obtained equation that decrease of the interfacial tension at the water-organic solvent interface must lead to a decrease in the interfacial activity of hydrophobic surfactants present in the system

  17. Structure Characterization and Properties of Metal-Surfactant Complexes Dispersed in Organic Solvents.

    Science.gov (United States)

    de la Iglesia, Pablo; Jaeger, Vance W; Xi, Yuyin; Pfaendtner, Jim; Pozzo, Lilo D

    2015-08-25

    This work describes the synthesis and characterization of metal-surfactant complexes. Dioctyl sulfosuccinate and dodecylbenzenesulfonate are associated with multivalent aluminum, iron, and vanadium ions using an ion exchange reaction. The metal complexes are dispersible in various organic solvents. In solvents with low polarity, the complexes form "inverse" macromolecular structures with multiple metal ions. In contrast, in alcohols, the complex size is reduced, showing a more disperse conformation. The metal and surfactant ions are still strongly bonded to each other in all the solvents probed. Small-angle X-ray and neutron scattering (SAXS and SANS) are used to characterize the structures. Simultaneous fitting of neutron and X-ray scattering spectra is performed in order to obtain an accurate description of the system. Scattering results are also validated by performing molecular dynamics (MD) simulations. The conductive and electrochemical properties of the complexes in solution are also evaluated. The dispersion of metal-organic complexes significantly increases electric conductivity, and some metal ions in the core of the complexes are shown to be electrochemically active in apolar solvents.

  18. Role of α-Helical Structure in Organic Solvent-Activated Homodimer of Elastase Strain K

    Directory of Open Access Journals (Sweden)

    Chee Fah Wong

    2011-09-01

    Full Text Available Recombinant elastase strain K overexpressed from E. coli KRX/pCon2(3 was purified to homogeneity by a combination of hydrophobic interaction chromatography and ion exchange chromatography, with a final yield of 48% and a 25-fold increase in specific activity. The purified protein had exhibited a first ever reported homodimer size of 65 kDa by SDS-PAGE and MALDI-TOF, a size which is totally distinct from that of typically reported 33 kDa monomer from P. aeruginosa. The organic solvent stability experiment had demonstrated a stability pattern which completely opposed the rules laid out in previous reports in which activity stability and enhancement were observed in hydrophilic organic solvents such as DMSO, methanol, ethanol and 1-propanol. The high stability and enhancement of the enzyme in hydrophilic solvents were explained from the view of alteration in secondary structures. Elastinolytic activation and stability were observed in 25 and 50% of methanol, respectively, despite slight reduction in α-helical structure caused upon the addition of the solvent. Further characterization experiments had postulated great stability and enhancement of elastase strain K in broad range of temperatures, pHs, metal ions, surfactants, denaturing agents and substrate specificity, indicating its potential application in detergent formulation.

  19. Unusual H-type aggregation of coumarin-481 dye in polar organic solvents.

    Science.gov (United States)

    Verma, Poonam; Pal, Haridas

    2013-11-27

    Coumarin-481 (C481) dye shows intriguing time-resolved (TR) fluorescence behavior in polar organic solvents of both protic and aprotic nature, namely, ethanol (EtOH) and acetonitrile (ACN), demonstrating the presence of multiple emitting species in the solution. Following concentration-dependent and wavelength-dependent TR fluorescence measurements and the time-resolved emission spectra (TRES) and time-resolved area-normalized emission spectra (TRANES) subsequently constructed using wavelength dependent decay parameters, we convincingly conclude that in the studied solvents a part of the dissolved dye undergoes H-type of aggregation, even at a very low dye concentration. This is quite an unusual finding because the dye C481 apparently shows reasonably good solubility in these organic solvents. As the TR measurements indicate, major contribution in the fluorescence decays is due to monomeric dye, having reasonably short lifetime (∼0.64-0.68 ns), which is in accordance with the conversion of fluorescent intramolecular charge transfer (ICT) state to nonfluorescent twisted intramolecular charge transfer (TICT) state suggested for the dye in high polarity solvents, causing an efficient nonradiative deexcitation. The minor contributions arising from the aggregated dyes show its clear presence in the decays at the blue edge of the emission spectra and have relatively longer lifetimes (∼1.2-5.2 ns) because the steric hindrance caused by the stacked dyes resists the ICT to TICT conversion. Aggregation of C481 dye as observed in the present study in polar organic solvents is an intriguing finding, as the dye is a widely used fluorescent probe for various photochemical studies, where overlooking such aggregation can mislead the observed results. PMID:24168239

  20. Partitioning and budget of inorganic and organic chlorine observed by MIPAS-B and TELIS in the Arctic in January 2010 and March 2011

    Science.gov (United States)

    Wetzel, Gerald; Birk, Manfred; de Lange, Arno; Oelhaf, Hermann; Friedl-Vallon, Felix; Kirner, Oliver; Kleinert, Anne; Maucher, Guido; Nordmeyer, Hans; Orphal, Johannes; Ruhnke, Roland; Sinnhuber, Björn-Martin

    2014-05-01

    Arctic winters 2009/2010 and 2010/2011 were characterized by strong vortices with extremely cold temperatures in the lower stratosphere above northern Scandinavia. Hence, the occurrence of widespread polar stratospheric clouds enabled a strong activation of chlorine compounds (ClOx) which rapidly destroyed ozone when sunlight returned after winter solstice. MIPAS (Michelson Interferometer for Passive Atmospheric Sounding) balloon measurements obtained in northern Sweden on 24 January 2010 and 31 March 2011 inside the polar vortices have provided vertical profiles of inorganic and organic chlorine species as well as diurnal variations of ClO around sunrise over the whole altitude range in which chlorine is undergoing activation and deactivation. The first flight was carried out in very cold chlorine-activated air with widespread polar stratospheric clouds. The second one was performed at the end of the winter during the last phase of ClOx deactivation. The Terahertz and submillimeter Limb Sounder TELIS was mounted on the MIPAS balloon gondola. TELIS is able to detect the chlorine species ClO and HCl. The complete inorganic and organic chlorine partitioning and budget in the stratosphere has been derived by combining MIPAS-B and TELIS simultaneously observed molecules. Observations are compared and discussed with calculations performed with the 3-dimensional Chemistry Climate Model EMAC (ECHAM5/MESSy Atmospheric Chemistry).

  1. Partitioning and budget of inorganic and organic chlorine species observed by MIPAS-B and TELIS in the Arctic in March 2011

    Science.gov (United States)

    Wetzel, G.; Oelhaf, H.; Birk, M.; de Lange, A.; Engel, A.; Friedl-Vallon, F.; Kirner, O.; Kleinert, A.; Maucher, G.; Nordmeyer, H.; Orphal, J.; Ruhnke, R.; Sinnhuber, B.-M.; Vogt, P.

    2015-07-01

    The Arctic winter 2010/2011 was characterized by a persistent vortex with extremely low temperatures in the lower stratosphere above northern Scandinavia leading to a strong activation of chlorine compounds (ClOx) like Cl, Cl2, ClO, ClOOCl, OClO, and HOCl, which rapidly destroyed ozone when sunlight returned after winter solstice. The MIPAS-B (Michelson Interferometer for Passive Atmospheric Sounding) and TELIS (TErahertz and submillimeter LImb Sounder) balloon measurements obtained in northern Sweden on 31 March 2011 inside the polar vortex have provided vertical profiles of inorganic and organic chlorine species as well as diurnal variations of ClO around sunrise over the whole altitude range in which chlorine has been undergoing activation and deactivation. This flight was performed at the end of the winter during the last phase of ClOx deactivation. The complete inorganic and organic chlorine partitioning and budget for 31 March 2011, assumed to be representative for the late-winter Arctic stratosphere, has been derived by combining MIPAS-B and TELIS simultaneously observed molecules. A total chlorine amount of 3.41 ± 0.30 parts per billion by volume is inferred from the measurements (above 24 km). This value is in line with previous stratospheric observations carried out outside the tropics confirming the slightly decreasing chlorine amount in the stratosphere. Observations are compared and discussed with the output of a multi-year simulation performed with the chemistry climate model EMAC (ECHAM5/MESSy Atmospheric Chemistry). The simulated stratospheric total chlorine amount is in accordance with the MIPAS-B/TELIS observations, taking into account the fact that some chlorine source gases and very short-lived species are not included in the model.

  2. Partitioning and budget of inorganic and organic chlorine species observed by MIPAS-B and TELIS in the Arctic in March 2011

    Directory of Open Access Journals (Sweden)

    G. Wetzel

    2015-02-01

    Full Text Available The Arctic winter 2010/11 was characterized by a persisting vortex with extremely cold temperatures in the lower stratosphere above northern Scandinavia leading to a strong activation of chlorine compounds (ClOx like Cl, Cl2, ClO, ClOOCl, OClO, and HOCl which rapidly destroyed ozone when sunlight returned after winter solstice. MIPAS (Michelson Interferometer for Passive Atmospheric Sounding and TELIS (Terahertz and submillimeter Limb Sounder balloon measurements obtained in northern Sweden on 31 March 2011 inside the polar vortex have provided vertical profiles of inorganic and organic chlorine species as well as diurnal variations of ClO around sunrise over the whole altitude range in which chlorine is undergoing activation and deactivation. This flight was performed at the end of the winter during the last phase of ClOx deactivation. The complete inorganic and organic chlorine partitioning and budget in the stratosphere has been derived by combining MIPAS-B and TELIS simultaneously observed molecules. A total chlorine amount of 3.41 ± 0.30 ppbv is inferred from the measurements. This value is in line with previously carried out stratospheric observations confirming the slightly decreasing chlorine trend in the stratosphere. Observations are compared and discussed with the output of a multi-year simulation performed with the Chemistry Climate Model EMAC (ECHAM5/MESSy Atmospheric Chemistry. The simulated stratospheric total chlorine amount is in accordance with the MIPAS-B/TELIS observation taking into account the fact that some chlorine source gases and very short lived species are not included in the model.

  3. Interactively interfacial reaction of iron-reducing bacterium and goethite for reductive dechlorination of chlorinated organic compounds

    Institute of Scientific and Technical Information of China (English)

    LI XiaoMin; LI YongTao; LI FangBai; ZHOU ShunGui; FENG ChunHua; LIU TongXu

    2009-01-01

    The interactively interfacial reactions between the iron-reducing bacterium (Shewanella decolorationis,S12) and iron oxide (α-FeOOH) were investigated to determine reductive dechlorination transformation of chlorinated organic compounds (chloroform and pentachlorophenol).The results showed that the interactive system of S12+ α-FeOOH exhibited relatively high dechlorination rate.By comparison,the S12 biotic system alone had no obvious dechlorination,and the α-FeOOH abiotic system showed low dechlorination rate.The enhanced dechlorination of chloroform and pentachlorophenol in the interactive system of S12+α-FeOOH was derived from the promoted generation of adsorbed Fe(Ⅱ) by S12.A decrease in redox potential of the Fe (Ⅲ)/Fe (Ⅱ) couple in the interactive reaction system was determined by cyclic voltammetry.Our results will give new insight into interactively interfacial reaction between iron-reducing bacterium and iron oxides for degradation of chlorinated organic compounds under anaerobic condition.

  4. Changes in dissolved organic matter fluorescence and disinfection byproduct formation from UV and subsequent chlorination/chloramination.

    Science.gov (United States)

    Lyon, Bonnie A; Cory, Rose M; Weinberg, Howard S

    2014-01-15

    Ultraviolet (UV) irradiation is being increasingly used to help drinking water utilities meet finished water quality regulations, but its influence on disinfection byproduct (DBP) precursors and DBP formation is not completely understood. This study investigated the effect of medium pressure (MP) UV combined with chlorination/chloramination on the fluorescent fraction of dissolved organic matter (DOM) isolated from a United States surface water with median total organic carbon content. Parallel factor analysis was used to understand how UV may alter the capacity of DOM to form DBPs of potential human health concern. The production of chloral hydrate and cyanogen chloride from MP UV followed by chlorine or chloramine, respectively, correlated with a decrease in fluorescence intensity of a protein/tryptophan-like component (R(2)=0.79-0.99) and a humic-like component (R(2)=0.91-1.00). This suggests that the UV-induced precursors to these compounds originated from DOM with similar characteristics to these components. The fluorescent DOM components identified in this study are similar to reoccurring components that have been previously identified in a range of raw and treated waters, and this work demonstrates the value of using fluorescence analysis of DOM to understand the relationships between DOM source and DBP formation under a range of treatment conditions.

  5. Effect of some organic solvents on oxidative phosphorylation in rat liver mitochondria

    DEFF Research Database (Denmark)

    Syed, Muzeeb; Skonberg, Christian; Hansen, Steen Honoré

    2013-01-01

    The effect of acetone, acetonitrile, dimethyl sulfoxide (DMSO), ethanol and methanol on oxidative phosphorylation (ATP synthesis) in rat liver mitochondria has been studied. All the organic solvents inhibited the oxidative phosphorylation in a concentration dependent manner, but with differences...... in potencies. Among the tested organic solvents, acetonitrile and acetone were more potent than ethanol, methanol, and DMSO. There was no significant difference in oxidative phosphorylation, compared to controls, when the concentrations of acetone was below 1% (v/v), of acetonitrile below 2% (v/v), of DMSO...... below 10% (v/v), of ethanol below 5% or of methanol below 2%, respectively. There was complete inhibition of oxidative phosphorylation at 50% (v/v) of acetone, acetonitrile and ethanol. But in the case of DMSO and methanol there were some residual activities observed at the 50% concentration level. DMSO...

  6. One-pot hydrothermal preparation of graphene sponge for the removal of oils and organic solvents

    Science.gov (United States)

    Wu, Ruihan; Yu, Baowei; Liu, Xiaoyang; Li, Hongliang; Wang, Weixuan; Chen, Lingyun; Bai, Yitong; Ming, Zhu; Yang, Sheng-Tao

    2016-01-01

    Graphene sponge (GS) has found applications in oil removal due to the hydrophobic nature of graphene sheets. Current hydrothermal preparations of GS use toxic reducing reagents, which might cause environmental pollution. In this study, we reported that graphene oxide (GO) could be hydrothermally reduced by glucose to form GS for the adsorption of oils and various organic solvents. Graphene sheets were reduced by glucose during the hydrothermal treatment and formed 3D porous structure. GS efficiently adsorbed organic solvents and oils with competitive adsorption capacities. GS was able to treat pollutants in pure liquid form and also in the simulated seawater. GS could be easily regenerated by evaporating or burning. After 10 cycles, the adsorption capacity still retained 77% by evaporating and 87% by burning. The implication to the applications of GS in water remediation is discussed.

  7. Graphene/polyester staple composite for the removal of oils and organic solvents

    Science.gov (United States)

    Wu, Ruihan; Yu, Baowei; Liu, Xiaoyang; Li, Hongliang; Bai, Yitong; Ming, Zhu; Chen, Lingyun; Yang, Sheng-Tao; Chang, Xue-Ling

    2016-06-01

    Spongy graphene has been widely applied in oil removal. However, spongy graphene is hardly applicable for crude oil removal, because the complexity and high viscosity of crude oil. Herein, we reported that graphene/polyester staple composite (GPSC) could be used for the removal of oils and organic solvents, in particular crude oil. Graphene oxide was in situ reduced in the presence of polyester staple by hydrazine hydrate to form GPSC. GPSC efficiently adsorbed oils and organic solvents with high adsorption capacities. Demonstrations of treating pure oils and those in simulated sea water by GPSC were successfully performed. Due to the loose structure, GPSC adsorbed crude oil quickly with an adsorption capacity of 52 g g-1. During the regeneration, the adsorption capacity of GPSC retained around 78% of the initial capacity up to 9 cycles. The implication to the applications of GPSC in water remediation is discussed.

  8. Organic compounds of different extractability in total solvent extracts from soils of contrasting water repellency

    Science.gov (United States)

    Atanassova, Irena; Doerr, Stefan H.

    2010-05-01

    Previous studies examining organic compounds that may cause water-repellent behaviour of soils have typically focussed on analysing only the lipophilic fraction of extracted material. This study aimed to provide a more comprehensive examination by applying single- and sequential-accelerated solvent extraction (ASE), separation and analysis by GC/MS of the total solvent extracts of three soils taken from under eucalypt vegetation with different levels of water repellency. Water repellency increased in all the soils after extraction with DCM:MeOH (95:5), but was eliminated with iso-propanol/ammonia (95:5). Quantities of major lipid compound classes varied between solvents and soils. Iso-propanol/ammonia (95:5) solvent released saccharides, glycerol, aromatic acids and other polar organic compounds, which were more abundant in fractionated extracts from the single extraction and the third step sequential ASE extraction, than in the extracts from the DCM:MeOH ASE solvent. Dominant compounds extracted from all soils were long-chain alkanols (>C22), palmitic acid, C29 alkane, β-sitosterol, terpenes, terpenoids and other polar compounds. The soil with smallest repellency lacked >C18 fatty acids and had smallest concentrations of alkanols (C26, C28 and C30) and alkanes (C29, C31), but a greater abundance of more complex polar compounds than the more repellent soils. We therefore speculate that the above compounds play an important role in determining the water repellency of the soils tested. The results suggest that one-stage and sequential ASE extractions with iso-propanol:ammonia and subsequent fractionation of extracts are a useful approach in providing a comprehensive assessment of the potential compounds involved in causing soil water repellency.

  9. Archaeal Inorganic Pyrophosphatase Displays Robust Activity under High-Salt Conditions and in Organic Solvents

    OpenAIRE

    McMillan, Lana J.; Hepowit, Nathaniel L.; Maupin-Furlow, Julie A.

    2016-01-01

    Soluble inorganic pyrophosphatases (PPAs) that hydrolyze inorganic pyrophosphate (PPi) to orthophosphate (Pi) are commonly used to accelerate and detect biosynthetic reactions that generate PPi as a by-product. Current PPAs are inactivated by high salt concentrations and organic solvents, which limits the extent of their use. Here we report a class A type PPA of the haloarchaeon Haloferax volcanii (HvPPA) that is thermostable and displays robust PPi-hydrolyzing activity under conditions of 25...

  10. Neurotoxic effects of organic solvents among workers in paint and lacquer manufacturing industry

    Directory of Open Access Journals (Sweden)

    Jovanović Jovica M.

    2004-01-01

    Full Text Available Introduction Organic solvents are chemically different compounds with one common feature: they dissolve fats, oils, resins, cellulose acetate and cellulose nitrate, which makes them widely used in industry. Most often organic solvents are used in paint and lacquer industries, in production of pesticides, plastics, explosives, rubber, cellulose, air conditioners, in pharmaceutical industry and in leather industry. The aim of this research was to analyze the working environment and professional hazards in paint and lacquer manufacturing industry and evaluate effects of chronic exposure to mixture of organic solvents on nervous system of exposed workers. Methodology The exposed group consisted of 50 workers professionally exposed to these noxae, while the control group consisted of 30 workers who have never been exposed to these noxae. Results Examination of working environment in departments of paint and lacquer manufacturing revealed presence of white spirit and toluene above allowed levels. Exposed workers more frequently complained of fatigue, hand numbness, enhanced excitation, and concentration difficulties, forgetfulness and headaches, than workers from the control group. Electroneurographic examination of n. medianus showed reduced motor and sensitive conduction velocity among exposed in comparison to workers from the control group. Reduced motor and sensitive conduction velocity was correlated with duration of exposure to these noxae. Terminal latency of n. medianus was statistically, significantly longer in the exposed group than in the control group. Workers in the exposed group have statistically significantly longer reaction time in response to acoustic and visual stimuli. Discussion Segmental demyelination and axonal degeneration, as forms of damage to peripheral nerves, were identified as responsible for peripheral neuropathy associated with occupational exposure to organic solvents. Conclusion Results of this study show possible

  11. Psychophysical Evaluation of Achromatic and Chromatic Vision of Workers Chronically Exposed to Organic Solvents

    OpenAIRE

    Luiz Carlos de Lima Silveira; Dora Fix Ventura; Lauro José Barata de Lima; Cláudio Eduardo Correa Teixeira; Anderson Raiol Rodrigues; Eliza Maria da Costa Brito Lacerda; Monica Gomes Lima

    2012-01-01

    The purpose of this paper was to evaluate achromatic and chromatic vision of workers chronically exposed to organic solvents through psychophysical methods. Thirty-one gas station workers (31.5 ± 8.4 years old) were evaluated. Psychophysical tests were achromatic tests (Snellen chart, spatial and temporal contrast sensitivity, and visual perimetry) and chromatic tests (Ishihara's test, color discrimination ellipses, and Farnsworth-Munsell 100 hue test—FM100). Spatial contrast sensitivities of...

  12. Lignin Peroxidase Oxidation of Aromatic Compounds in Systems Containing Organic Solvents

    OpenAIRE

    Vazquez-Duhalt, Rafael; Westlake, Donald W. S.; Fedorak, Phillip M.

    1994-01-01

    Lignin peroxidase from Phanerochaete chrysosporium was used to study the oxidation of aromatic compounds, including polycyclic aromatic hydrocarbons and heterocyclic compounds, that are models of moieties of asphaltene molecules. The oxidations were done in systems containing water-miscible organic solvents, including methanol, isopropanol, N, N-dimethylformamide, acetonitrile, and tetrahydrofuran. Of the 20 aromatic compounds tested, 9 were oxidized by lignin peroxidase in the presence of hy...

  13. Reduction of organic solvent emission by industrial use of electron-beam curable coatings

    International Nuclear Information System (INIS)

    Most industrial finishing processes operate by the use of liquid organic coating materials drying by solvent evaporation and subsequent chemical crosslinking reactions, in many cases also releasing cleavage products. These organic emissions contribute to air pollution and therefore many countries have issued restrictions in order to protect the environment. Complementary to other modern methods for reducing this problem, radiation chemistry enables an approach by radical chain polymerization which can be induced by exposure to electron radiation. This procedure is known as electron-beam curing of coatings or the EBC process. It utilizes well-developed accelerator equipment with voltages of 150 to 400kV at a minimum energy consumption. There is no necessity to use irradiation facilities based on the decay of radioisotopes. Free radical polymerization requires unsaturated resins as pain binders and polymerizable liquid compounds (monomers) as reactive diluents. Their crosslinking yields a high molecular network, the coating, without any emission of organic solvents or cleavage products. Moreover, the radiochemical formation of the paint film occurs extremely rapidly. The technical application of EBC coatings began by coating automotive plastic parts; a little later the finishing of wood products gained more industrial use as a non-polluting and energy-saving coating technology. Application methods in coating plastic foils in combination with vacuum metallizing and the production of decorative laminating papers for furniture followed. In 1981 new EBC pilot lines were installed for curing top coats on PVC foil and also for the coating of prefinished steel wheels for automobiles. In comparison with conventional solvent-based methods the industrial EBC process results in a nearly complete reduction of organic solvent emission avoiding air pollution and saving valuable petrochemical raw materials. This paper reviews the development of EBC during the last decade. (author)

  14. DETERMINATION OF CHLORINATED ORGANIC COMPOUNDS IN THE MAIN DRAINAGE CHANNEL OF KONYA

    Directory of Open Access Journals (Sweden)

    Mehmet Emin AYDIN

    2000-03-01

    Full Text Available The main drainage channel of Konya collects drainage waters from farmlands of Konya and discharges to the salt lake. Since there is not any city municipal sewarage system in Konya sewage of the city also discharged to the main drainage channel. Along the channel, farmers use the channels water for irrigation purposes. Therefore a through examination of wastewater and determination of chlorinated compounds were necessary. In this research, analyses were carried by gas chromatography (GC on water samples collected hourly, daily and monthly from the channel.

  15. Coacervate Core Micelles for the Dispersion and Stabilization of Organophosphate Hydrolase in Organic Solvents

    Science.gov (United States)

    Mills, Carolyn; Obermeyer, Allie; Dong, Xuehui; Olsen, Bradley D.

    Bulk organophosphate (OP) nerve agents are difficult to decontaminate on site and dangerous to transport. The organophosphate hydrolase (OPH) enzyme is an efficient catalyst for hydrolyzing, and thus decontaminating, these compounds, but suffers from poor stability in the hydrophobic bulk OP environment. Here, we exploit the complex coacervation phase separation phenomenon to form complex coacervate core micelles (C3Ms) that can protect this OPH enzyme under these conditions. Stable C3Ms form when mixing a charged-neutral block copolymer methyl-quaternized poly(4-vinylpyridine)-block-poly(oligo(ethylene glycol) methacrylate) (Qp4vp- b-POEGMA), a homopolymer poly(acrylic acid) (PAA), and OPH under a certain conditions. The C3Ms are then transferred into two organic solvents, ethanol and dimethyl methylphosphonate (DMMP), which is a good simulant for the physical properties of the OP compounds. The C3Ms retain their nanostructures in the organic solvents. The activity test of OPH indicates that the C3Ms successfully protect OPH activity in organic solvents.

  16. Organic solvents as interferents in arsenic determination by hydride generation atomic absorption spectrometry with flame atomization

    Science.gov (United States)

    Karadjova, Irina B.; Lampugnani, Leonardo; Dědina, Jiri; D'Ulivo, Alessandro; Onor, Massimo; Tsalev, Dimiter L.

    2006-05-01

    Interference effects of various organic solvents miscible with water on arsenic determination by hydride generation atomic absorption spectrometry have been studied. Arsine was chemically generated in continuous flow hydride generation system and atomized by using a flame atomizer able to operate in two modes: miniature diffusion flame and flame-in-flame. The effects of experimental variables and atomization mode were investigated: tetrahydroborate and hydrochloric acid concentrations, argon, hydrogen and oxygen supply rates for the microflame, and the distance from the atomization region to the observation zone. The nature of the species formed in the flame due to the pyrolysis of organic solvent vapors entering the flame volume together with arsine is discussed. The observed signal depression in the presence of organic solvents has been mainly attributed to the atomization interference due to heterogeneous gas-solid reaction between the free arsenic atoms and finely dispersed carbon particles formed by carbon radicals recombination. The best tolerance to interferences was obtained by using flame-in-flame atomization (5-10 ml min - 1 of oxygen flow rate), together with higher argon and hydrogen supply rates and elevated observation heights.

  17. Purification and Characterization of Organic Solvent and Detergent Tolerant Lipase from Thermotolerant Bacillus sp. RN2

    Directory of Open Access Journals (Sweden)

    Tadahiko Kajiwara

    2010-09-01

    Full Text Available The aim of this study was to characterize the organic solvent and detergent tolerant properties of recombinant lipase isolated from thermotolerant Bacillus sp. RN2 (Lip-SBRN2. The isolation of the lipase-coding gene was achieved by the use of inverse and direct PCR. The complete DNA sequencing of the gene revealed that the lip-SBRN2 gene contains 576 nucleotides which corresponded to 192 deduced amino acids. The purified enzyme was homogeneous with the estimated molecular mass of 19 kDa as determined by SDS-PAGE and gel filtration. The Lip-SBRN2 was stable in a pH range of 9–11 and temperature range of 45–60 °C. The enzyme was a non metallo-monomeric protein and was active against pNP-caprylate (C8 and pNP-laurate (C12 and coconut oil. The Lip-SBRN2 exhibited a high level of activity in the presence of 108% benzene, 102.4% diethylether and 112% SDS. It is anticipated that the organic solvent and detergent tolerant enzyme secreted by Bacillus sp. RN2 will be applicable as catalysts for reaction in the presence of organic solvents and detergents.

  18. Enhancement of the aspartame precursor synthetic activity of an organic solvent-stable protease.

    Science.gov (United States)

    Ogino, Hiroyasu; Tsuchiyama, Shotaro; Yasuda, Masahiro; Doukyu, Noriyuki

    2010-03-01

    The PST-01 protease is highly stable and catalyzes the synthesis of the aspartame precursor with high reaction yields in the presence of organic solvents. However, the synthesis rate using the PST-01 protease was slower than that observed when thermolysin was used. Structural comparison of both enzymes showed particular amino acid differences near the active center. These few residue differences in the PST-01 protease were mutated to match those amino acid types found in thermolysin. The mutated PST-01 proteases at the 114th residue from tyrosine to phenylalanine showed enhancement of synthetic activity. This activity was found to be similar to thermolysin. In addition, mutating the residue in the PST-01 protease with arginine and serine showed more improvement of the activity. The mutant PST-01 protease should be more useful than thermolysin for the synthesis of the aspartame precursor, because this enzyme has higher stability and activity in the presence of organic solvents. The results show the potential of organic solvent-stable enzymes as industrial catalysts.

  19. [Cloning and expression of organic solvent tolerant lipase gene from Staphylococcus saprophyticus M36].

    Science.gov (United States)

    Tang, Yanchong; Lu, Yaping; Lü, Fengxia; Bie, Xiaomei; Guo, Yao; Lu, Zhaoxin

    2009-12-01

    Lipases are important biocatalysts that are widely used in food processing and bio-diesel production. However, organic solvents could inactivate some lipases during applications. Therefore, the efficient cloning and expression of the organic solvent-tolerant lipase is important to its application. In this work, we first found out an organic solvent-tolerant lipase from Staphylococcus saprophyticus M36 and amplified the 741 bp Lipase gene lip3 (GenBank Accession No. FJ979867), by PCR, which encoded a 31.6 kD polypeptide of 247 amino acid residues. But the lipase shared 83% identity with tentative lip3 gene of Staphylococcus saprophyticus (GenBank Accession No. AP008934). We connected the gene with expression vector pET-DsbA, transformed it into Escherichia coli BL21 (DE3), and obtained the recombinant pET-DsbA-lip3. With the induction by 0.4 mmol/L of isopropyl beta-D-thiogalactopyranoside at pH 8.0, OD600 1.0, 25 degrees C for 12 h, the lipase activity reached up to 25.8 U/mL. The lipase expressed was stable in the presence of methanol, n-hexane, and isooctane, n-heptane.

  20. Towards safer sodium-ion batteries via organic solvent/ionic liquid based hybrid electrolytes

    Science.gov (United States)

    Monti, Damien; Ponrouch, Alexandre; Palacín, M. Rosa; Johansson, Patrik

    2016-08-01

    Hybrid electrolytes aimed at application in sodium-ion batteries (SIB) consisting of an organic solvent mixture (EC:PC) and different ionic liquids (ILs); EMImTFSI, BMImTFSI, and Pyr13TFSI, and with the NaTFSI salt providing the Na+ charge carriers have here been extensively studied. The physico-chemical and electrochemical characterisation includes ionic conductivity, viscosity, density, cation coordination and solvation, various safety measures, and electrochemical stability window (ESW). Hybrid electrolytes with 10-50% of IL content were found to have ionic conductivities on par with comparable organic solvent based electrolytes, but with highly enhanced safety properties. A systematic Raman spectroscopy study of the cation coordination and solvation before and after electrolyte safety tests by ignition suggest that IL cations and TFSI remain stable when ignited while organic solvents are consumed. Finally, the solid electrolyte interphase (SEI) formed when using hybrid electrolytes has both better mechanical and electrochemical stability than the SEI derived from pure IL based electrolytes. For a half-cell with a hard carbon (HC) electrode and a hybrid electrolyte with a composition of 0.8 m NaTFSI in EC0.45:PC0.45:Pyr13TFSI0.10 encouraging results were obtained for IL based electrolytes - ca. 182 mAhg-1 at C/10 over 40 cycles.

  1. A Robust and Cost-Effective Superhydrophobic Graphene Foam for Efficient Oil and Organic Solvent Recovery.

    Science.gov (United States)

    Zhu, Haiguang; Chen, Dongyun; An, Wei; Li, Najun; Xu, Qingfeng; Li, Hua; He, Jinghui; Lu, Jianmei

    2015-10-21

    Water pollution caused by chemical reagent leaking, industrial wastewater discharging, and crude oil spills has raised global concerns on environmental sustainability, calling for high-performance absorbent materials for effective treatments. However, low-cost materials capable of effectively separating oils and organic solvents from water with a high adsorption capacity and good recyclability are rare on the market. Here, a cost-effective method is reported to fabricate high-performance graphene modified absorbents through the facile thermal reduction of graphene oxide on the skeletons of melamine foam. By integrating the high porosity, superior elasticity, and mechanical stability of raw sponge with the chemical stability and hydrophobicity of graphene sheets, the as-fabricated graphene foam not only possesses a rough and superhydrophobic surface, but also exhibits an excellent adsorption performance and extraordinary recyclability for various oils and organic solvents. It is worth mentioning that the superhydrophobic surface also endows the graphene foam with an excellent efficiency for oil/water separation. More importantly, the cost-effective fabrication method without involving expensive raw materials and sophisticated equipment permits a scale-up of the graphene foam for pollution disposal. All these features make the graphene foam an ideal candidate for removal and collection of oils and organic solvents from water. PMID:26265103

  2. Effects of organic solvents on the enzyme activity of Trypanosoma cruzi glyceraldehyde-3-phosphate dehydrogenase in calorimetric assays

    DEFF Research Database (Denmark)

    Wiggers, Henrik; Cheleski, J; Zottis, A;

    2007-01-01

    .0% for MeOH and up to 7.5% for DMSO. The results show that when GAPDH is assayed in the presence of DMSO (5%, v/v) using the ITC experiment, the enzyme exhibits approximately twofold higher activity than that of GAPDH with no cosolvent added. When MeOH (5%, v/v) is the cosolvent, the GAPDH activity......In drug discovery programs, dimethyl sulfoxide (DMSO) is a standard solvent widely used in biochemical assays. Despite the extensive use and study of enzymes in the presence of organic solvents, for some enzymes the effect of organic solvent is unknown. Macromolecular targets may be affected...... by the presence of different solvents in such a way that conformational changes perturb their active site structure accompanied by dramatic variations in activity when performing biochemical screenings. To address this issue, in this work we studied the effects of two organic solvents, DMSO and methanol (Me...

  3. Carbon, hydrogen and nitrogen isotopes in solvent-extractable organic matter from carbonaceous chondrites

    Science.gov (United States)

    Becker, R. H.; Epstein, S.

    1982-01-01

    CCl4 and CH3OH solvent extractions were performed on the Murray, Murchison, Orgueil and Renazzo carbonaceous chondrites. Delta-D values of +300-+500% are found in the case of the CH3OH-soluble organic matter. The combined C, H and N isotope data makes it unlikely that the CH3OH-soluble components are derivable from, or simply related to, the insoluble organic polymer found in the same meteorites. A relation between the event that formed hydrous minerals in CI1 and CM2 meteorites and the introduction of water- and methanol-soluble organic compounds is suggested. Organic matter soluble in CCl4 has no N, and delta-C-13 values are lower than for CH3OH-soluble phases. It is concluded that there either are large isotopic fractionations for carbon and hydrogen between different soluble organic phases, or the less polar components are partially of terrestrial origin.

  4. [Liver function of workers occupationally exposed to mixed organic solvents in a petrochemical industry].

    Science.gov (United States)

    Fernández-D'Pool, J; Oroño-Osorio, A

    2001-06-01

    A descriptive and cross sectional study was conducted to determine whether hepatic function changes in workers occupationally exposed to a mixture of organic solvents, were due to the exposure or confusing factors. A non random sample of 77 workers, operators and supervisors of the Olefin Plant I and II of a petrochemical industry in Maracaibo, Venezuela, was used. Their mean age was 29 +/- 7 years, and had at least one year of exposure to the solvents. This sample was compared with a group of employees of the administrative offices or control panel workers, with a mean age of 36 +/- 8 year and with similar anthropometric characteristics. Workers with a known history of liver disease, blood transfusions and diabetes mellitus were excluded of the study. In addition to a complete occupational disease medical history and a physical examination, serum samples were obtained to determine the activity of the aspartato aminotransferase (AST), alanin aminotransferase (ALT), gamma glutamiltransferase (GGT), alkaline phosphatase (AF), the concentration of the total bile acids (BAS), the surface antigen of hepatitis B(HbsAg) and the hepatitis A virus antibodies: AntiHAV-IgG and the AntiHAV-IgM. An urine sample was taken and analyzed by standard methodology to determine urinary phenols. The air concentrations of benzene, ethylbenzene, toluene and xylene were analyzed by gas chromathography. The serum activities of the liver enzymes, the concentration of bile acids and urinary phenols were not influenced by the exposure to the solvents. The increase of the activity of GGT was associated with obesity and alcohol consumption. The antibodies of the surface antigen of hepatitis A-IgM were normal in both groups and the antibodies for the antigen of hepatitis A-IgG presented a prevalence of 6% in the exposed group and 9% in the non exposed not being associated with liver abnormalities. The individual air concentrations of the solvents were below the environmentally permissible

  5. Activity of α-Chymotrypsin Enhanced in the Presence of Iron Oxide Nanoparticles in Organic Solvent: Application to Peptide Synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Cheolwoo; Kim, Mahnjoo [Pohang Univ. of Science and Technology, Pohang (Korea, Republic of)

    2013-03-15

    We have demonstrated that α-CT displays a significantly enhanced activity in the presence of IONs relative to its IONs-free counterparts in organic solvent. IONs-activated α-CT catalyzed efficiently the synthesis of peptides without the formation of hydrolyzed byproducts. Enzymes are a useful class of catalysts for the preparation of enantiomeric compounds. The applications of enzymes in synthetic transformations, however, are limited by their reduced activities in organic solvent. Particularly, proteases such as subtilisin and α-chymotrypsin display several orders of magnitude lower activities in organic solvent than their aqueous counterparts.

  6. Nickel-Catalyzed Suzuki-Miyaura Cross-Coupling in a Green Alcohol Solvent for an Undergraduate Organic Chemistry Laboratory

    Science.gov (United States)

    Hie, Liana; Chang, Jonah J.; Garg, Neil K.

    2015-01-01

    A modern undergraduate organic chemistry laboratory experiment involving the Suzuki-Miyaura coupling is reported. Although Suzuki-Miyaura couplings typically employ palladium catalysts in environmentally harmful solvents, this experiment features the use of inexpensive nickel catalysis, in addition to a "green" alcohol solvent. The…

  7. SOLVENT POLARITY AND INTERNAL STRESSES CONTROL THE SWELLING BEHAVIOUR OF GREEN WOOD DURING DEHYDRATION IN ORGANIC SOLUTION

    Directory of Open Access Journals (Sweden)

    Shanshan Chang,

    2012-04-01

    Full Text Available The dimensional variations of green wood samples induced by organic solvents have been studied. The solvents used (ethanol, isopropanol, acetone, and acetonitrile covered a wide range of polarity and were studied pure and in aqueous solutions over a wide range of concentrations. Samples of normal and tension wood of poplar were used in order to minimize the effect of hydrophobic extractives on the wood-solvent interactions. The evolution of wood volume and of tangential strain with the concentration of the organic solvents shows a behavior similar to gels, with a significant swelling for solutions of intermediate polarity. The similarity of volume obtained in water and less polar pure organic solvents strikingly contrasted the different effects of water and organic solvents on dry wood. Low-polarity solvents were extremely effective in the stress release of tension wood, as indicated by the pattern of longitudinal shrinkage. Solvent exchange does not affect the mesoporous structure of the cell walls of tension wood and is a promising way to reduce internal stress in wood products.

  8. Effect of water-miscible organic solvents on CYP450-mediated metoprolol and imipramine metabolism in rat liver microsomes

    Directory of Open Access Journals (Sweden)

    T S Shah

    2015-01-01

    Full Text Available The catalytic activity of cytochrome P450 enzymes is known to be affected by presence of organic solvents in in vitro assays. However, these effects tend to be variable and depend on the substrate and CYP450 isoform in question. In the present study, we have investigated effect of ten water miscible organic solvents (methanol, ethanol, propanol, isopropanol, acetone, acetonitrile, dimethylsulphoxide, dimethylformamide, dioxane and PEG400 on water soluble substrates of CYP450, metoprolol and imipramine, at 0, 0.1, 0.25, 0.5, 0.75 and 1% v/v concentration in rat liver microsomes. Organic solvents studied had a concentration dependent inhibitory effect on the metoprolol and imipramine metabolism activity. Metoprolol metabolism was found to be more susceptible to the organic solvents, almost all the ten solvents had more or less inhibitory effect compared to imipramine metabolism. Except acetone, PEG400 and dimethylsulphoxide, all solvents had ~50% inhibition of total metoprolol metabolism activity, while in case of imipramine metabolism activity, only n-propanol, isopropanol and PEG400 had ~50% inhibition at 1% v/v. Interestingly, methanol, dimethylsulphoxide and acetonitrile had negligible effect on the imipramine metabolism (less than 10% inhibition at 1% v/v while, total metoprolol metabolism activity was substantially inhibited by these solvents (MeOH 52%, DMSO 29% and ACN 47% at 1% v/v. In both cases, dioxane was found to be the most inhibitory solvent (~90% inhibition at 1% v/v.

  9. Thermodynamics of solvent interaction with the metal-organic framework MOF-5.

    Science.gov (United States)

    Akimbekov, Zamirbek; Wu, Di; Brozek, Carl K; Dincă, Mircea; Navrotsky, Alexandra

    2016-01-14

    The inclusion of solvent in metal-organic framework (MOF) materials is a highly specific form of guest-host interaction. In this work, the energetics of solvent MOF-5 interactions has been investigated by solution calorimetry in 5 M sodium hydroxide (NaOH) at room temperature. Solution calorimetric measurement of enthalpy of formation (ΔH(f)) of Zn4O(C8H4O4)3·C3H7NO (MOF-5·DMF) and Zn4O(C8H4O4)3·0.60C5H11NO (MOF-5·0.60DEF) from the dense components zinc oxide (ZnO), 1,4-benzenedicarboxylic acid (H2BDC), N,N-dimethylformamide (DMF) and N,N-diethylformamide (DEF) gives values of 16.69 ± 1.21 and 45.90 ± 1.46 kJ (mol Zn4O)(-1), respectively. The enthalpies of interaction (ΔH(int)) for DMF and DEF with MOF-5 are -82.78 ± 4.84 kJ (mol DMF)(-1) and -89.28 ± 3.05 kJ (mol DEF)(-1), respectively. These exothermic interaction energies suggest that, at low guest loading, Lewis base solvents interact more strongly with electron accepting Zn4O clusters in the MOF than at high solvent loading. These data provide a quantitative thermodynamic basis to investigate transmetallation and solvent assisted linker exchange (SALE) methods and to synthesize new MOFs. PMID:26658672

  10. Production of an osteoinductive demineralised bone matrix powder without the use of organic solvents.

    Science.gov (United States)

    Eagle, M J; Rooney, P; Kearney, J N

    2015-09-01

    Demineralised bone matrix (DBM) is produced by grinding cortical bone into a powder, sieving the powder to obtain a desired size range and then demineralising the powder using acid. Protocols for the production of DBM powder have been published since 1965 and the powder can be used in lyophilised form or it can be mixed with a carrier to produce a paste or putty. The powder is generally produced from cortical bone which has been processed to remove blood, bone marrow and bone marrow components, including fat. Removal of fat is accomplished by incorporating incubation in an organic solvent, often chloroform, chloroform/methanol or acetone. The use of organic solvents in a clean room environment in a human tissue bank is problematic and involves operator exposure and the potential for the solvent to be trapped in air filters or recirculated throughout the clean room suite. Consequently, in this study, we have developed a cortical bone washing step which removes fat/lipid without the use of an organic solvent. Bone was prepared from six femoral shafts from three donors by dissecting soft tissue and bisecting the shaft, the shafts were then cut into ~9-10 cm lengths. These struts were then taken through a series of hot water washes at 56-59 °C, centrifugation and decontamination steps. Washed cortical struts were then lyophilised before being ground with a compressed air milling machine. The ground bone was sieved, demineralised, freeze-dried and terminally sterilised with a target dose of 25 kGy gamma irradiation. The DBM powder was evaluated for residual calcium content, in vitro cytotoxicity and osteoinductivity by implantation into the muscle of an athymic mouse. Data indicated that in addition to removing in excess of 97% DNA and extractable soluble protein, the washing protocol reduced lipid 10,000-fold. The processed bone was easily ground without clogging the grinder; the sterilised DBM powder was not cytotoxic but was osteoinductive in the animal model

  11. The effect of solvent on the kinetics of the oxidation of benzaldehydes by quinolinium chlorochromate in aqueous organic solvent media

    Directory of Open Access Journals (Sweden)

    G. FATIMA JEYANTHI

    2002-12-01

    Full Text Available The kinetics of the oxidation of benzaldehyde and para-substituted benzaldehydes by quinolinium chlorochromate in water-dimethylformamide mixtures has been studied under pseudo-first-order conditions at 25±0.2°C. The operation of non-specific and specific solvent-solute interactions was explored by correlating the rate data with solvent parameters through a correlation analysis technique. Both electron-releasing and electron-withdrawing substitutents enhance the rate of oxidation and the Hammett plot shows a break in the reactivity order indicating the applicability of a dual mechanism.

  12. Effect of water miscible organic solvents on p-nitrophenol hydroxylase (CYP2E1 activity in rat liver microsomes

    Directory of Open Access Journals (Sweden)

    Pranali G Patil

    2015-01-01

    Full Text Available Organic solvents used for solubilization of the substrates/NCEs are known to affect the activity of cytochrome P450 enzymes. Further, this effect varies with the solvents used, the substrates and CYP450 isoforms in question. In the present study, we have investigated the effect of ten commonly used water miscible organic solvents (methanol, ethanol, 1-propanol, 2-propanol, acetonitrile, acetone, dimethyl sulphoxide, N,N-dimethyl formamide, dioxane and polyethylene glycol 400 on p-nitrophenol hydroxylase activity at 0, 0.1, 0.25, 0.5, 0.75 and 1% v/v concentration in rat liver microsomes. All the solvents studied showed concentration dependent inhibition of the p-nitrophenol hydroxylase activity except acetonitrile which showed activation of the activity at concentration range studied. Out of ten solvents studied, dioxane was found to be the most inhibitory solvent (inhibition >90% at 0.25% v/v concentration. Overall, solvents like dimethyl sulphoxide, dimethyl formamide and dioxane appeared to be unsuitable for characterizing p-nitrophenol hydroxylase (CYP2E1-mediated reactions due to a high degree of inhibition. On the other hand, methanol and acetonitrile at concentrations <0.5% v/v appeared to be appropriate solvents for substrate solubilization while evaluating CYP2E1-mediated catalysis. The results of this study imply that caution should be exercised while choosing solvents for dissolution of substrate during enzyme studies in liver microsomes.

  13. Synthesis and characterization of monodisperse CdSe quantum dots in different organic solvents

    Institute of Scientific and Technical Information of China (English)

    He Rong; You Xiaogang; Tian Hongye; Gao Feng; Cui Daxiang; Gu Hongchen

    2006-01-01

    Nearly monodisperse CdSe quantum dots (QDs)have been prepared by a soft solution approach using air-stable reagents in different organic solvents.This scheme is a supplement to the conventional thermal decomposition of organometailic compounds at higher temperatures.CdSe nanocrystals of different sizes could be obtained by simply changing the solvent.This method is reproducible and simple and thus can be readily scaled up for industrial production.The reaction process was monitored by the temporal evolution of the UV-Vis absorption and room temperature photoluminensce spectra.The structures of the CdSe quantum dots were determined by X-ray powder diffraction (XRD) and transmission electron microscopy (TEM).The phase-transfer of oleic acid-stabilized CdSe nanocrystals into PBS buffer solutions was also studied for their potentials in biological applications.

  14. Ionic Liquids Beyond Simple Solvents: Glimpses at the State of the Art in Organic Chemistry.

    Science.gov (United States)

    Kuchenbuch, Andrea; Giernoth, Ralf

    2015-12-01

    Within the last 25 years ionic liquids have written a tremendous success story, which is documented in a nearly uncountable amount of original research papers, reviews, and numerous applications in research and industry. These days, ionic liquids can be considered as a mature class of compounds for many different applications. Frequently, they are used as neoteric solvents for chemical tansformations, and the number of reviews on this field of research is huge. In this focused review, though, we are trying to evaluate the state of the art of ionic liquid chemistry beyond using them simply as solvents for chemical transformations. It is not meant to be a comprehensive overview on the topic; the choice of emphasis and examples rather refects the authors' personal view on the field. We are especially highlighting fields in which we believe the most fundamental developments within the next five years will take place: biomass processing, (chiral) ionic liquids from natural sources, biotransformations, and organic synthesis.

  15. Reversible brain damage following acute organic solvents' poisoning determined by magnetic resonance

    Directory of Open Access Journals (Sweden)

    Dujmović Irena

    2005-01-01

    Full Text Available Introduction. Acute exposure to the effects of volatile solvents is characterized by the abrupt onset of symptoms and signs of poisoning, and relatively fast recovery in the majority of cases. Case report. We report a 24-year-old patient with an acute, accidental poisoning with a mixture of volatile organic solvents (most probably toluene, styrene and xylene, which led to the development of upward gaze paresis, diplopia, hemiparesis, ataxic gate, and the late onset truncal ataxia episodes. After 6 weeks, he recovered completely, while his extensive brain MRI lesions in the caudate nuclei, laterobasal putaminal regions, bilateral anterior insular cortex, central midbrain tegmental area withdrew completely after 4 months. Conclusion. Acute toxic encephalopathy should be a part of the differential diagnosis in any patient with acute neurobehavioral and neurological deficit.

  16. Hydrothermal liquefaction of palm oil empty fruit bunch (EFB) into bio-oil in different organic solvents

    Science.gov (United States)

    Sarwono, Rakhman; Pusfitasari, Eka Dian; Ghozali, Muhammad

    2016-06-01

    Thermochemical Liquefaction of empty fruit bunch (EFB) of palm oil in different organic solvents (water, methanol, ethanol, acetone, toluene and hexane) were comparatively investigated. Experiments were carried out in an autoclave at different temperatures of 300, 350 and 400 °C with a fixed solid/liquid rasio of 3 gram in 50 ml solvent, without catalysts and reaction time of 5 hours. The efficiency of above solvents in terms of conversion rate, soluble liquid and carbon products were investigated in the experiments. Increasing the reaction temperature increased the conversion rate in all organic solvents and water, but gaseous products also increased using a reaction temperature of 400 oC. The water solvent gave higher conversion rate of 49.14%, while toluene, acetone, methanol, hexane and ethanol gave conversion of 35.76%, 26.5%, 25.98%, 24.26 %, and 22.24%, respectively. The bio-oil produced in order of the largest amount were using methanol, water, ethanol, toluene, acetone, and hexane solvents. The chemical properties of bio-oil products were significantly affected by the type of liquefaction solvent. The composition of bio-oil consisted of mostly of a mixture of organic acids, ketones, and esters. The methanol and ethanol solvents resulted in mostly esters, while toluene and hexane resulted in mostly organic acids. Acetone solvent resulted in the same amount of organic acid and esters. In water as a solvent resulted in 2-pentanone, 4-hydroxy-4-methyl. The bio-oil consisted of a range of carbon C6 - C20 fragments.

  17. Application of natural deep eutectic solvents to the extraction of anthocyanins from Catharanthus roseus with high extractability and stability replacing conventional organic solvents.

    Science.gov (United States)

    Dai, Yuntao; Rozema, Evelien; Verpoorte, Robert; Choi, Young Hae

    2016-02-19

    Natural deep eutectic solvents (NADES) have attracted a great deal of attention in recent times as promising green media. They are generally composed of neutral, acidic or basic compounds that form liquids of high viscosity when mixed in certain molar ratio. Despite their potential, viscosity and acid or basic nature of some ingredients may affect the extraction capacity and stabilizing ability of the target compounds. To investigate these effects, extraction with a series of NADES was employed for the analysis of anthocyanins in flower petals of Catharanthus roseus in combination with HPLC-DAD-based metabolic profiling. Along with the extraction yields of anthocyanins their stability in NADES was also studied. Multivariate data analysis indicates that the lactic acid-glucose (LGH), and 1,2-propanediol-choline chloride (PCH) NADES present a similar extraction power for anthocyanins as conventional organic solvents. Furthermore, among the NADES employed, LGH exhibits an at least three times higher stabilizing capacity for cyanidins than acidified ethanol, which facilitates their extraction and analysis process. Comparing NADES to the conventional organic solvents, in addition to their reduced environmental impact, they proved to provide higher stability for anthocyanins, and therefore have a great potential as possible alternatives to those organic solvents in health related areas such as food, pharmaceuticals and cosmetics. PMID:26822320

  18. Investigation of electrochemical degradation and application of e-paper dyes in organic solvents

    Institute of Scientific and Technical Information of China (English)

    Luhai LI; Ming WANG; Yi FANG; Shunan QIAO

    2009-01-01

    To avoid environmental pollution due to organic dye solutions, the electrophoresis and degradation of dye in organic solvents such as alcohol were investigated. Many dyes were tested in the Indium tin oxide (ITO) electrode driving cell, and about 15 dyes moved under voltage driving. Both the curves of ultraviolet-visible (UV-Vis) and infrared (IR) spectra of the electrophoresis samples showed that the metal complexes Red 04 and Acid Black 1 were degradable in alcohol solution by electrochemical reaction. The cyclic volt-ampere curves of the samples from the electrochemical working station proved that electrochemical reactions took place. Based on the analysis of UV-Vis and IR spectra, the electrochemical degradation products of azo and metal complex azo dyes at lower voltage driving (1-5 V) in organic solvents are oxidized azobenzene, not hydrazine, which was found in the electrochemical degradation of dye water solutions. When the ITO electrode is modified by a polyimide (PI) film to a thickness less than 4 μm, the electrochemical degradation of the dye in alcohol solution will not appear in the cyclic volt-ampere curves. A dye electrophoresis in organic solution flexible prototype e-paper display was formed and the display picture is shown.

  19. Influences of Organic Solvents on Particle Size and Drug-loading Efficiency for 5-Fluorouracil Poly(lactic acid) Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    LIUXiao-yan; CHANGJin; GUOYan-shuang; YUANXu-bo; LIXiao-rong; LIUChun-ling; SONGCun-xian

    2004-01-01

    The objective of this study was to investigate the influences of organic solvents on particle size, drug content, loading efficiency and yield for 5-Fluorouracil Poly (lactic acid) nanoparticles . The 5-Fluorouracil was entrapped into poly(lactic acid)(PLA) nanoparticles using a water-in-oil-in-water solvent evaporation technique. During the preparation process, ethyl acetate and acetone were used as organic solvents since they are less toxic than the more commonly used dichloromethane. The effect of the three solvents on particle size, drug content, loading efficiency and yield of nanopartcles was compared. When the solvent of the oil phase was acetone, the highest drug content, smallest particle size and lowest yield were obtained for the PLA nanoparticles.

  20. Reaction of bromine and chlorine with phenolic compounds and natural organic matter extracts--Electrophilic aromatic substitution and oxidation.

    Science.gov (United States)

    Criquet, Justine; Rodriguez, Eva M; Allard, Sebastien; Wellauer, Sven; Salhi, Elisabeth; Joll, Cynthia A; von Gunten, Urs

    2015-11-15

    Phenolic compounds are known structural moieties of natural organic matter (NOM), and their reactivity is a key parameter for understanding the reactivity of NOM and the disinfection by-product formation during oxidative water treatment. In this study, species-specific and/or apparent second order rate constants and mechanisms for the reactions of bromine and chlorine have been determined for various phenolic compounds (phenol, resorcinol, catechol, hydroquinone, phloroglucinol, bisphenol A, p-hydroxybenzoic acid, gallic acid, hesperetin and tannic acid) and flavone. The reactivity of bromine with phenolic compounds is very high, with apparent second order rate constants at pH 7 in the range of 10(4) to 10(7) M(-1) s(-1). The highest value was recorded for the reaction between HOBr and the fully deprotonated resorcinol (k = 2.1 × 10(9) M(-1) s(-1)). The reactivity of phenolic compounds is enhanced by the activating character of the phenolic substituents, e.g. further hydroxyl groups. With the data set from this study, the ratio between the species-specific rate constants for the reactions of chlorine versus bromine with phenolic compounds was confirmed to be about 3000. Phenolic compounds react with bromine or chlorine either by oxidation (electron transfer, ET) or electrophilic aromatic substitution (EAS) processes. The dominant process mainly depends on the relative position of the hydroxyl substituents and the possibility of quinone formation. While phenol, p-hydroxybenzoic acid and bisphenol A undergo EAS, hydroquinone, catechol, gallic acid and tannic acid, with hydroxyl substituents in ortho or para positions, react with bromine by ET leading to quantitative formation of the corresponding quinones. Some compounds (e.g. phloroglucinol) show both partial oxidation and partial electrophilic aromatic substitution and the ratio observed for the pathways depends on the pH. For the reaction of six NOM extracts with bromine, electrophilic aromatic substitution

  1. Comparative responses of river biofilms at the community level to common organic solvent and herbicide exposure.

    Science.gov (United States)

    Paule, A; Roubeix, V; Swerhone, G D W; Roy, J; Lauga, B; Duran, R; Delmas, F; Paul, E; Rols, J L; Lawrence, J R

    2016-03-01

    Residual pesticides applied to crops migrate from agricultural lands to surface and ground waters. River biofilms are the first aquatic non-target organisms which interact with pesticides. Therefore, ecotoxicological experiments were performed at laboratory scale under controlled conditions to investigate the community-level responses of river biofilms to a chloroacetanilide herbicide (alachlor) and organic solvent (methanol) exposure through the development referenced to control. Triplicate rotating annular bioreactors, inoculated with river water, were used to cultivate river biofilms under the influence of 1 and 10 μg L(-1) of alachlor and 25 mg L(-1) of methanol. For this purpose, functional (thymidine incorporation and carbon utilization spectra) and structural responses of microbial communities were assessed after 5 weeks of development. Structural aspects included biomass (chlorophyll a, confocal laser scanning microscopy) and composition (fluor-conjugated lectin binding, molecular fingerprinting, and diatom species composition). The addition of alachlor resulted in a significant reduction of bacterial biomass at 1 μg L(-1), whereas at 10 μg L(-1), it induced a significant reduction of exopolymer lectin binding, algal, bacterial, and cyanobacterial biomass. However, there were no changes in biofilm thickness or thymidine incorporation. No significant difference between the bacterial community structures of control and alachlor-treated biofilms was revealed by terminal restriction fragment length polymorphism (T-RFLP) analyses. However, the methanol-treated bacterial communities appeared different from control and alachlor-treated communities. Moreover, methanol treatment resulted in an increase of bacterial biomass and thymidine incorporation as well. Changes in dominant lectin binding suggested changes in the exopolymeric substances and community composition. Chlorophyll a and cyanobacterial biomass were also altered by methanol. This study suggested

  2. [Interconnection of physico-chemical characteristics of organic solvents and their denaturing ability in relation to proteins].

    Science.gov (United States)

    Belova, A B; Mozhaev, V V; Levashov, A V; Sergeeva, M V; Martinek, K; Khmel'nitskiĭ, Iu L

    1991-11-01

    Reversible denaturation of several proteins (alpha-chymotrypsin, trypsin, laccase, chymotrypsinogen, cytochrome c and myoglobin) by a broad series of organic solvents of different nature was studied. The regularities of this process were analyzed, employing both experimental and literary data based on the results of kinetic and spectroscopic measurements. In all the systems under study denaturation proceeded in a threshold manner, i. e., an abrupt change in the catalytic and/or spectroscopic properties of the dissolved proteins was observed after a certain threshold concentration of the organic solvent had been reached. To account for the observed features of the denaturation process, a thermodynamic model of reversible protein denaturation by organic solvents was proposed. This model is based on the widely accepted viewpoint that the undisturbed water shell around the protein globule is necessary for maintaining the dissolved protein in the native state. Quantitative analysis of the model led to an equation establishing a relationship between the threshold concentration of an organic solvent and its physico-chemical characteristics, such as hydrophobicity, solvating ability and molecular geometry. This equation fits well in the experimental data for all the proteins tested. Based on the above thermodynamic model of protein denaturation, a novel quantitative parameter characterizing the denaturing strength of organic solvents (termed as the denaturation capacity or DC) was proposed. Different organic solvents arranged according to their DC values form the DC scale of organic solvents which permits to predict theoretically the threshold concentration of any organic solvent for a given protein.(ABSTRACT TRUNCATED AT 250 WORDS) PMID:1666845

  3. Multidisciplinary investigation of the fate, transport, and remediation of chlorinated solvents in fractured rocks at the former Naval Air Warfare Center (NAWC): Scientific and management challenges, and strategies for a successful research program

    Science.gov (United States)

    Tiedeman, C. R.; Goode, D. J.; Shapiro, A. M.; Lacombe, P. J.; Chapelle, F. H.; Bradley, P. M.; Imbrigiotta, T. E.; Williams, J. H.; Curtis, G. P.; Hsieh, P. A.

    2008-12-01

    At the former Naval Air Warfare Center (NAWC) in West Trenton NJ, the U.S. Geological Survey, in cooperation with the U.S. Navy and under support from the Strategic Environmental Research and Development Program (SERDP), is investigating the fate, transport, and remediation of trichloroethylene (TCE) and its daughter products in dipping, fractured mudstones underlying the site. TCE concentrations in ground water are as high as ~100 mg/L. Objectives of multidisciplinary research at the NAWC include (1) understanding the physical, chemical, and microbiological processes and properties affecting the fate, transport, and removal of chlorinated solvents in fractured rocks, (2) assessing the efficiency of different remediation methods (pump and treat, natural and enhanced biodegradation), and (3) transferring the results to help remediate other contaminated fractured rock aquifers. There are numerous scientific and technical challenges to meeting these goals, including the extreme spatial variability of flow and transport properties at the NAWC and the complex distribution of contaminants, geochemical constituents, and microorganisms in fractures and the rock matrix. In addition, there are management challenges that are equally important to address in order to achieve a successful research program. These include balancing the requirements of the many parties involved at the site, including researchers, the site owner, and regulatory agencies; and ensuring that limited research funds are directed towards work that addresses the most important scientific questions as well as stakeholder concerns. Strategies for the scientific challenges at NAWC include developing a carefully planned program to characterize spatial variability in rock properties and groundwater constituents so that the data obtained are applicable to solving research questions focused on remediation. Strategies for the management challenges include fostering open lines of communication among all parties and

  4. Improved Production of Paclitaxel from Suspension Culture of Taxus chinensis var.mairei by in situ Extraction with Organic Solvents

    Institute of Scientific and Technical Information of China (English)

    未作君; 元英进; 吴兆亮; 吴金川

    2003-01-01

    The production of paclitaxel from suspension culture of Taxus chinensis var,mairei was improved by in situ extraction with organic solvents to avoid feedback repression and product degradation.Oleic acid and dibutyl phthalate were proved to be suitable solvents .The optimal volumetric percentage of organic solvents in the culture medium was found to be around 8%,and the favorable time for their introduction was at the exponential phase of cell growth,Paclitaxel production with the in situ extraction was ca 3-fold of that without extraction.

  5. Photo-dynamics of roseoflavin and riboflavin in aqueous and organic solvents

    Science.gov (United States)

    Zirak, P.; Penzkofer, A.; Mathes, T.; Hegemann, P.

    2009-03-01

    Roseoflavin (8-dimethylamino-8-demethyl- D-riboflavin) and riboflavin in aqueous and organic solvents are studied by optical absorption spectroscopy, fluorescence spectroscopy, and fluorescence decay kinetics. Solvent polarity dependent absorption shifts are observed. The fluorescence quantum yields are solvent dependent. For roseoflavin the fluorescence decay shows a bi-exponential dependence (ps to sub-ps time constant, and 100 ps to a few ns time constant). The roseoflavin photo-dynamics is explained in terms of fast intra-molecular charge transfer (diabatic electron transfer) from the dimethylamino electron donor group to the pteridin carbonyl electron acceptor followed by intra-molecular charge recombination. The fast fluorescence component is due to direct locally-excited-state emission, and the slow fluorescence component is due to delayed locally-excited-state emission and charge transfer state emission. The fluorescence decay of riboflavin is mono-exponential. The S 1-state potential energy surface is determined by vibronic relaxation and solvation dynamics due to excited-state dipole moment changes (adiabatic optical electron transfer).

  6. Photo-dynamics of roseoflavin and riboflavin in aqueous and organic solvents

    Energy Technology Data Exchange (ETDEWEB)

    Zirak, P. [Institut II - Experimentelle und Angewandte Physik, Universitaet Regensburg, Universitaetstrasse 31, D-93053 Regensburg (Germany); Penzkofer, A., E-mail: alfons.penzkofer@physik.uni-regensburg.de [Institut II - Experimentelle und Angewandte Physik, Universitaet Regensburg, Universitaetstrasse 31, D-93053 Regensburg (Germany); Mathes, T.; Hegemann, P. [Institut fuer Biologie/Experimentelle Biophysik, Humboldt Universitaet zu Berlin, Invalidenstrasse 42, D-10115 Berlin (Germany)

    2009-03-30

    Roseoflavin (8-dimethylamino-8-demethyl-D-riboflavin) and riboflavin in aqueous and organic solvents are studied by optical absorption spectroscopy, fluorescence spectroscopy, and fluorescence decay kinetics. Solvent polarity dependent absorption shifts are observed. The fluorescence quantum yields are solvent dependent. For roseoflavin the fluorescence decay shows a bi-exponential dependence (ps to sub-ps time constant, and 100 ps to a few ns time constant). The roseoflavin photo-dynamics is explained in terms of fast intra-molecular charge transfer (diabatic electron transfer) from the dimethylamino electron donor group to the pteridin carbonyl electron acceptor followed by intra-molecular charge recombination. The fast fluorescence component is due to direct locally-excited-state emission, and the slow fluorescence component is due to delayed locally-excited-state emission and charge transfer state emission. The fluorescence decay of riboflavin is mono-exponential. The S{sub 1}-state potential energy surface is determined by vibronic relaxation and solvation dynamics due to excited-state dipole moment changes (adiabatic optical electron transfer).

  7. Understanding the Dispersion and Assembly of Bacterial Cellulose in Organic Solvents.

    Science.gov (United States)

    Ferguson, Auren; Khan, Umar; Walsh, Melissa; Lee, Koon-Yang; Bismarck, Alexander; Shaffer, Milo S P; Coleman, Jonathan N; Bergin, Shane D

    2016-05-01

    The constituent nanofibrils of bacterial cellulose are of interest to many researchers because of their purity and excellent mechanical properties. Mechanisms to disrupt the network structure of bacterial cellulose (BC) to isolate bacterial cellulose nanofibrils (BCN) are limited. This work focuses on liquid-phase dispersions of BCN in a range of organic solvents. It builds on work to disperse similarly intractable nanomaterials, such as single-walled carbon nanotubes, where optimum dispersion is seen for solvents whose surface energies are close to the surface energy of the nanomaterial; bacterial cellulose is shown to disperse in a similar fashion. Inverse gas chromatography was used to determine the surface energy of bacterial cellulose, under relevant conditions, by quantifying the surface heterogeneity of the material as a function of coverage. Films of pure BCN were prepared from dispersions in a range of solvents; the extent of BCN exfoliation is shown to have a strong effect on the mechanical properties of BC films and to fit models based on the volumetric density of nanofibril junctions. Such control offers new routes to producing robust cellulose films of bacterial cellulose nanofibrils. PMID:27007744

  8. Biogas from MSW landfill: Composition and determination of chlorine content with the AOX (adsorbable organically bound halogens) technique

    International Nuclear Information System (INIS)

    An exhaustive characterization of the biogas from some waste disposal facilities has been carried out. The analysis includes the main components (methane, carbon dioxide, nitrogen and oxygen) as well as trace components such as hydrogen sulphide, ammonia and VOCs (volatile organic compounds) including siloxanes and halogenated compounds. VOCs were measured by GC/MS (Gas Chromatography/Mass Spectrometry) using two different procedures: thermal desorption of the Tenax TA and Carbotrap 349 tubes and SPME (Solid Phase Micro-Extraction). A method has been established to measure the total halogen content of the biogas with the AOX (adsorbable organically bound halogens) technique. The equipment used to analyze the samples was a Total Organic Halogen Analyzer (TOX-100). Similar results were obtained when comparing the TOX (Total Organic Halogen) values with those obtained by GC/MS. The halogen content in all the samples was under 22 mg Cl/Nm3 which is below the limit of 150 mg/Nm3 proposed in the Spanish Regulations for any use of the biogas. The low chlorine content in the biogas studied, as well as the low content of other trace compounds, makes it suitable for use as a fuel for electricity generating engines

  9. Self-diffusion coefficients for water and organic solvents at high temperatures along the coexistence curve

    Science.gov (United States)

    Yoshida, Ken; Matubayasi, Nobuyuki; Nakahara, Masaru

    2008-12-01

    The self-diffusion coefficients D for water, benzene, and cyclohexane are determined by using the pulsed-field-gradient spin echo method in high-temperature conditions along the liquid branch of the coexistence curve: 30-350 °C (1.0-0.58 g cm-3), 30-250 °C (0.87-0.56 g cm-3), and 30-250 °C (0.77-0.48 g cm-3) for water, benzene, and cyclohexane, respectively. The temperature and density effects are separated and their origins are discussed by examining the diffusion data over a wide range of thermodynamic states. The temperature dependence of the self-diffusion coefficient for water is larger than that for organic solvents due to the large contribution of the attractive hydrogen-bonding interaction in water. The density dependence is larger for organic solvents than for water. The difference is explained in terms of the van der Waals picture that the structure of nonpolar organic solvents is determined by the packing effect due to the repulsion or exclusion volumes. The dynamic solvation shell scheme [K. Yoshida et al., J. Chem. Phys. 127, 174509 (2007)] is applied for the molecular interpretation of the translational dynamics with the aid of molecular dynamics simulation. In water at high temperatures, the velocity relaxation is not completed before the relaxation of the solvation shell (mobile-shell type) as a result of the breakdown of the hydrogen-bonding network. In contrast, the velocity relaxation of benzene is rather confined within the solvation shell (in-shell type).

  10. Solvent extraction of scandium from lateritic nickel- cobalt ores using different organic reagents

    Directory of Open Access Journals (Sweden)

    Ferizoğlu Ece

    2016-01-01

    Full Text Available Scandium is the most important and strategic metal that can be recovered as a by-product from lateritic nickel-cobalt ores. In this research, different extractants were investigated in order to extract scandium from a sulfate medium by a using a solvent extraction method. Generally, the organic extractants are classified as acidic, neutral and basic organophosphorus compounds. However, in solvent extraction of scandium, the acidic and neutral organophosphorus compounds are preferred due to their higher extraction efficiencies. Thus, the aim of the present study was to compare the scandium extraction efficiencies of some acidic and neutral organic reagents. For this reason, Ionquest 290 (Bis(2,4,4-trimethylpenthyl phosphonic acid, DEHPA (Di(2-ethylhexyl phosphoric acid, Cyanex 272 ((Bis(2,4,4-trimethylpentyl phosphinic acid which are acidic organophosphorus compounds, and Cyanex 923 (Trialkylphosphine oxide, which is a neutral organophosphorus compound, were used. The extraction capacities of these organics were studied with respect to the extractant concentration at same pH and phase ratio. As a result of the study, DEHPA was found to have higher scandium extraction efficiency with lower iron extraction at pH = 0.55 at a phase ratio of 10:1 = A:O.

  11. Solvent recycle/recovery

    Energy Technology Data Exchange (ETDEWEB)

    Paffhausen, M.W.; Smith, D.L.; Ugaki, S.N.

    1990-09-01

    This report describes Phase I of the Solvent Recycle/Recovery Task of the DOE Chlorinated Solvent Substitution Program for the US Air Force by the Idaho National Engineering Laboratory, EG G Idaho, Inc., through the US Department of Energy, Idaho Operations Office. The purpose of the task is to identify and test recovery and recycling technologies for proposed substitution solvents identified by the Biodegradable Solvent Substitution Program and the Alternative Solvents/Technologies for Paint Stripping Program with the overall objective of minimizing hazardous wastes. A literature search to identify recycle/recovery technologies and initial distillation studies has been conducted. 4 refs.

  12. Study of the resolution of amino acids and aminoalcohols in organic solvents.

    Science.gov (United States)

    Orsini, F; Pelizzoni, F; Ghioni, C

    1995-06-01

    The enzymatic resolution of racemic phenylglycine, phenylglycinol and phenylalaninol has been studied in organic solvents under a variety of experimental conditions. Subtilisin in 3-methyl-3-pentanol was effective for the resolution of phenylglycine esters, via N-acylation with trifluoroethyl butyrate. Porcine pancreatic lipase in ethyl acetate gave satisfactory results in the resolution of phenylglycinol and phenylalaninol; theα orβ position of the phenyl group was found to influence both the rate and the chemioselectivity of the reaction. PMID:24178813

  13. Antimicrobial Activity of Organic Solvent Extracts of Three Marine Macroalgae From Chilika Lake, Orissa, India

    Directory of Open Access Journals (Sweden)

    Patra, J. K.

    2009-01-01

    Full Text Available In vitro study of antibacterial activity of organic solvent extracts of three marine macroalgae viz., Chaetomorpha linum (Mell Kuetzing, Enteromorpha compressa (L Greville and Polysiphonia subtilissima Mont. showed specific activity in inhibiting the growth of three Gram-negative bacteria (Shigella flexneri, Vibrio cholerae and Escherichia coli and two Gram positive bacteria (Bacillus subtilis and Bacillus brevis. The results revealed that the chloroform and ethyl acetate extracts were active against most of the pathogens whereas methanol and ethanol extracts were active only against S. flexneri.

  14. Chemo-enzymatic peptide synthesis and derivatisation using Subtilisin A in anhydrous organic solvents

    OpenAIRE

    Nuijens, T.

    2012-01-01

    In this thesis it is demonstrated that Alcalase and Cal-B in neat organic solvent can perform unique and cost-efficient conversions that are useful in the peptide area. Not only can Alcalase be used to prepare several C-terminally derivatized amino acids and peptides (such as amides, esters and arylamides), this protease is also a very efficient catalyst for peptide bond formation (optionally combined with Cal-B for ester synthesis) or even for fully enzymatic peptide synthesis strategies bas...

  15. Purification and Characterization of Haloalkaline, Organic Solvent Stable Xylanase from Newly Isolated Halophilic Bacterium-OKH

    OpenAIRE

    Sanghvi, Gaurav; Jivrajani, Mehul; Patel, Nirav; Jivrajani, Heta; Bhaskara, Govinal Badiger; Patel, Shivani

    2014-01-01

    A novel, alkali-tolerant halophilic bacterium-OKH with an ability to produce extracellular halophilic, alkali-tolerant, organic solvent stable, and moderately thermostable xylanase was isolated from salt salterns of Mithapur region, Gujarat, India. Identification of the bacterium was done based upon biochemical tests and 16S rRNA sequence. Maximum xylanase production was achieved at pH 9.0 and 37°C temperature in the medium containing 15% NaCl and 1% (w/v) corn cobs. Sugarcane bagasse and whe...

  16. Synthesis and characterization of CdSe colloidal quantum dots in organic solvent

    International Nuclear Information System (INIS)

    In this paper we present experimental results on preparation and characterization of colloidal CdSe quantum dots in organic solvent. CdSe QDs were synthesized following a modified literature method. CdSe QDs were isolated by adding acetone to the cooled solution followed by centrifugation. CdSe QDs have been characterized by UV-Vis absorption and photoluminescent (PL) spectroscopy. The average CdSe particles size estimated from the UV-Vis absorption spectra was found to be in the range 2.28-2.92 nm which is in good agreement with PL measurements. (authors)

  17. SYNTHESIS AND CHARACTERIZATION OF CdSe COLLOIDAL QUANTUM DOTS IN ORGANIC SOLVENT

    OpenAIRE

    Ion Geru; Olga Bordian; Constantin Loshmansky; Ion Culeac; Constantin Turta

    2014-01-01

    In this paper we present experimental results on preparation and characterization of colloidal CdSe quantum dots in organic solvent. CdSe QDs were synthesized following a modified literature method. CdSe QDs were isolated by adding acetone to the cooled solution followed by centrifugation. CdSe QDs have been characterized by UV-Vis absorption and photoluminescent (PL) spectroscopy. The average CdSe particles size estimated from the UV-Vis absorption spectra was found to be in the rang...

  18. SYNTHESIS AND CHARACTERIZATION OF CdSe COLLOIDAL QUANTUM DOTS IN ORGANIC SOLVENT

    Directory of Open Access Journals (Sweden)

    Ion Geru

    2014-06-01

    Full Text Available In this paper we present experimental results on preparation and characterization of colloidal CdSe quantum dots in organic solvent. CdSe QDs were synthesized following a modified literature method. CdSe QDs were isolated by adding acetone to the cooled solution followed by centrifugation. CdSe QDs have been characterized by UV-Vis absorption and photoluminescent (PL spectroscopy. The average CdSe particles size estimated from the UV-Vis absorption spectra was found to be in the range 2.28-2.92 nm which is in good agreement with PL measurements.

  19. Analysis of organic solvents and liquid mixtures using a fiber-tip evaporation sensor

    Science.gov (United States)

    Preter, Eyal; Donlagic, Denis; Artel, Vlada; Katims, Rachel A.; Sukenik, Chaim N.; Zadok, Avi

    2014-05-01

    The instantaneous size and rate of evaporation of pendant liquid droplets placed on the cleaved facet of a standard fiber are reconstructed based on reflected optical power. Using the evaporation dynamics, the relative contents of ethanol in ethanol-water binary mixtures are assessed with 1% precision and different blends of methanol in gasoline are properly recognized. The latter application, in particular, is significant for the use of alternative fuels in the automotive sector. Also, ten organic solvents are identified based on their evaporation from a fiber facet coated with a hydrophobic, selfassembled monolayer.

  20. Cation-π Interaction between the Aromatic Organic Counterion and DTAB Micelle in Mixed Solvents

    Institute of Scientific and Technical Information of China (English)

    DENG,Dong-Shun(邓东顺); LI,Hao-Ran(李浩然); LIU,Di-Xia(刘迪霞); HAN,Shi-Jun(韩世钧)

    2004-01-01

    The cation-π interaction between the aromatic organic counterion potassium hydrogen phthalate (KHP) and DTAB micelle in aqueous mixture of EG was investigated, using the techniques of conductivity measurements, UV absorption spectrum and NMR spectrum. The conductivity and UV spectrum studies were with respect to the effect of KHP on DTAB and that of DTAB micelle on KHP, respectively. According to the chemical shift changes of the aromatic ring and the surfactant methylene protons, it can be assumed that KHP penetrated into DTAB micelle with its carboxylic group protruding out of the micellar surface. And the strength of the interaction became weaker with the content of EG in the mixed solvent increasing.

  1. Resolution of 2-Octanol via Lipase-catalyzed Enantioselective Acetylation in Organic Solvents

    Institute of Scientific and Technical Information of China (English)

    WANG Zhi; LI Zheng-qiang; Yu Da-hai; WENG Liang; LIU Ming; ZHANG Gui-rong; CAO Shu-gui

    2004-01-01

    The lipases from different sources were screened for their ability to catalyze the resolution of 2-octanol in organic solvents with vinyl acetate as the acylating reagent. The medium effect has been studied on the irreversible transesterification with varying water activity(aw). The influence of vinyl acetate concentration on it has also been investigated. Under the optimal conditions, the enantiomeric ratio(E value) of pseudomonas fluorescence lipase(PFL) exceeded 200 with an enantiomeric excess(e. e. ) of S-2-octanol above 99% at a 51% degree of conversion.

  2. Response of Rhodococcus erythropolis strain IBBPo1 to toxic organic solvents

    Directory of Open Access Journals (Sweden)

    Mihaela Marilena Stancu

    2015-12-01

    Full Text Available Abstract Recently, there has been a lot of interest in the utilization of rhodococci in the bioremediation of petroleum contaminated environments. This study investigates the response of Rhodococcus erythropolis IBBPo1 cells to 1% organic solvents (alkanes, aromatics. A combination of microbiology, biochemical, and molecular approaches were used to examine cell adaptation mechanisms likely to be pursued by this strain after 1% organic solvent exposure. R. erythropolis IBBPo1 was found to utilize 1% alkanes (cyclohexane, n-hexane, n-decane and aromatics (toluene, styrene, ethylbenzene as the sole carbon source. Modifications in cell viability, cell morphology, membrane permeability, lipid profile, carotenoid pigments profile and 16S rRNA gene were revealed in R. erythropolis IBBPo1 cells grown 1 and 24 h on minimal medium in the presence of 1% alkanes (cyclohexane, n-hexane, n-decane and aromatics (toluene, styrene, ethylbenzene. Due to its environmental origin and its metabolic potential, R. erythropolis IBBPo1 is an excellent candidate for the bioremediation of soils contaminated with crude oils and other toxic compounds. Moreover, the carotenoid pigments produced by this nonpathogenic Gram-positive bacterium have a variety of other potential applications.

  3. Removal of polycyclic aromatic hydrocarbons from organic solvents by ashes wastes

    International Nuclear Information System (INIS)

    Polycyclic aromatic hydrocarbons (PAHs) can be formed during the refinery processes of crude petroleum. Their removal is of great importance. The same happens with other organic solvents used for the extraction of PAHs (hexane, acetonitrile...), which can be polluted with PAHs. Kinetic and equilibrium batch sorption tests were used to investigate the effect of wood ashes wastes as compared to activated carbon on the sorption of three representative PAHs from n-hexane and acetonitrile. Mussel shell ashes were discarded for batch sorption experiments because they were the only ashes containing PAHs. The equilibrium time was reached at 16 h. Physical sorption caused by the aromatic nature of the compounds was the main mechanism that governed the PAHs removal process. Our investigation revealed that wood ashes obtained at lower temperature (300 deg. C) did not show any PAHs sorption, while ashes obtained at higher temperature (>500 deg. C) have adsorbent sites readily available for the PAH molecules. An increase in the molecular weight of PAHs has a strong effect on sorption wood ashes wastes. As low the wood ashes particle size as high the sorption of PAHs, as a result of differences in adsorbent sites. The performance of wood ash wastes vs. activated carbon to remove 10 PAHs from organic solvents is competitive in price, and a good way for waste disposal.

  4. Enantioselective hydrolysis of epichlorohydrin using whole Aspergillus niger ZJB-09173 cells in organic solvents

    Indian Academy of Sciences (India)

    Huo-Xi Jin; Zhong-Ce Hu; Yu-Guo Zheng

    2012-09-01

    The enantioselective hydrolysis of racemic epichlorohydrin for the production of enantiopure ()-epichloro-hydrin using whole cells of Aspergillus niger ZJB-09173 in organic solvents was investigated. Cyclohexane was used as the reaction medium based on the excellent enantioselectivity of epoxide hydrolase from A. niger ZJB-09173 in cyclohexane. However, cyclohexane had a negative effect on the stability of epoxide hydrolase from A. niger ZJB-09173. In the cyclohexane medium, substrate inhibition, rather than product inhibition of catalysis, was observed in the hydrolysis of racemic epichlorohydrin using A. niger ZJB-09173. The racemic epichlorohydrin concentration was markedly increased by continuous feeding of substrate without significant decline of the yield. Ultimately, 18.5% of ()-epichlorohydrin with 98% enantiomeric excess from 153.6 mM of racemic epichlorohydrin was obtained by the dry cells of A. niger ZJB-09173, which was the highest substrate concentration in the production of enantiopure ()-epichlorohydrin by epoxide hydrolases using an organic solvent medium among the known reports.

  5. Synthesis of alkyl esters by cutinase in miniemulsion and organic solvent media.

    Science.gov (United States)

    de Barros, Dragana P C; Fonseca, Luís P; Cabral, Joaquim M S; Weiss, Clemens K; Landfester, Katharina

    2009-05-01

    The main objective of this work was studying and testing the nature and influence of reaction media (organic solvent vs. miniemulsion system) on the synthesis of alkyl esters catalyzed by Fusarium solani pisi cutinase. Ester synthesis and cutinase selectivity for different chain length of acids and alcohols (ethyl and hexyl) were evaluated. In iso-octane, after 1 h of reaction, cutinase exhibits rates of esterification between 0.24 micromol x mg(-)1 x min(-1) for ethyl oleate and 1.15 micromol x mg(-)1 x min(-1) for ethyl butyrate, while in a miniemulsion system the rates were from 0.05 for ethyl heptanoate to 0.76 micromol x mg(-1) x min(-1) for ethyl decanoate. The reaction rate for the synthesis of hexyl esters in a miniemulsion system was from 0.19 for hexyl heptanoate to 1.07 micromol x mg(-)1 x min(-1) for hexyl decanoate. High conversion yields of 95% at equilibrium after 8 h of reaction in iso-octane for pentanoic acid (C(5)) with ethanol at equimolar concentration (0.1 M) was achieved. Additionally, this work showed that a significant and unexpected shift in cutinase selectivity occurred towards longer chain length carboxylic acids (C(8)-C(10)) in miniemulsion system as compared to organic solvent (iso-octane) and previous studies in reverse micellar systems. The possibility of working with higher concentration of substrates, without inhibitory effect on the enzyme, was another advantage of the miniemulsion system.

  6. Occupational exposure to organic solvents: a risk factor for pulmonary veno-occlusive disease.

    Science.gov (United States)

    Montani, David; Lau, Edmund M; Descatha, Alexis; Jaïs, Xavier; Savale, Laurent; Andujar, Pascal; Bensefa-Colas, Lynda; Girerd, Barbara; Zendah, Inès; Le Pavec, Jerome; Seferian, Andrei; Perros, Frédéric; Dorfmüller, Peter; Fadel, Elie; Soubrier, Florent; Sitbon, Oliver; Simonneau, Gérald; Humbert, Marc

    2015-12-01

    Pulmonary veno-occlusive disease (PVOD) is a rare form of pulmonary hypertension characterised by predominant remodelling of pulmonary venules. Bi-allelic mutations in the eukaryotic translation initiation factor 2α kinase 4 (EIF2AK4) gene were recently described as the major cause of heritable PVOD, but risk factors associated with PVOD remain poorly understood. Occupational exposures have been proposed as a potential risk factor for PVOD, but epidemiological studies are lacking.A case-control study was conducted in consecutive PVOD (cases, n=33) and pulmonary arterial hypertension patients (controls, n=65). Occupational exposure was evaluated via questionnaire interview with blinded assessments using an expert consensus approach and a job exposure matrix (JEM).Using the expert consensus approach, PVOD was significantly associated with occupational exposure to organic solvents (adjusted OR 12.8, 95% CI 2.7-60.8), with trichloroethylene being the main agent implicated (adjusted OR 8.2, 95% CI 1.4-49.4). JEM analysis independently confirmed the association between PVOD and trichloroethylene exposure. Absence of significant trichloroethylene exposure was associated with a younger age of disease (54.8±21.4 years, p=0.037) and a high prevalence of harbouring bi-allelic EIF2AK4 mutations (41.7% versus 0%, p=0.015).Occupational exposure to organic solvents may represent a novel risk factor for PVOD. Genetic background and environmental exposure appear to influence the phenotypic expression of the disease. PMID:26541523

  7. Removal of endotoxins from bacteriophage preparations by extraction with organic solvents.

    Directory of Open Access Journals (Sweden)

    Bożena Szermer-Olearnik

    Full Text Available Lipopolysaccharide (LPS, endotoxin, pyrogen constitutes a very troubling contaminant of crude phage lysates produced in Gram-negative bacteria. Toxicity of LPS depends on the strong innate immunity response including the cytokines. Therefore, its removal is important for bacteriophage applications. In this paper, we present a procedure for extractive removal of endotoxin from bacteriophage preparations with water immiscible solvents (1-octanol or 1-butanol. During extraction most of the phage lytic activity is retained in the aqueous phase, while endotoxin accumulates in the organic solvent. The levels of endotoxin (expressed as endotoxin units, EU in the aqueous bacteriophage-containing fraction determined by limulus amebocyte lysate or EndoLISA assay were exceptionally low. While the initial endotoxin levels in the crude phage lysates ranged between 10(3 and 10(5 EU/ml the average level after organic extraction remaining in the aqueous fraction was 5.3 EU/ml. These values when related to phage titers decreased from 10(3-10(5 EU/10(9 PFU (plaque forming units down to an average of 2.8 EU/10(9 PFU. The purification procedure is scalable, efficient and applicable to all the bacteriophages tested: T4, HAP1 (E. coli and F8 (P. aeruginosa.

  8. Use of Organic Solvents to Extract Organochlorine Pesticides (OCPs) from Aged Contaminated Soils

    Institute of Scientific and Technical Information of China (English)

    YE Mao; JIN Xin; JIANG Xin; YANG Xing-Lun; SUN Ming-Ming; BIAN Yong-Rong; WANG Fang; GU Cheng-Gang; WEI Hai-Jiang; SONG Yang; WANG Lei

    2013-01-01

    Problems associated with organochlorine pesticide (OCP)-contaminated sites in China have received wide attention.To solve such problems,innovative ex-situ methods of site remediation are urgently needed.We investigated the feasibility of the extraction method with different organic solvents,ethanol,1-propanol,and three fractions of petroleum ether,using a soil collected from Wujiang (WJ),China,a region with long-term contamination of dichlorodiphenyltrichloroethanes (DDTs).We evaluated different influential factors,including organic solvent concentration,washing time,mixing speed,solution-to-soil ratio,and washing temperature,on the removal of DDTs from the WJ soil.A set of relatively better parameters were selected for extraction with 100 mL L-1 petroleum ether (60-90 ℃):washing time of 180 min,mixing speed of 100 r min-1,solution-to-soil ratio of 10:1,and washing temperature of 50 ℃.These selected parameters were also applied on three other seriously OCP-polluted soils.Results demonstrated their broad-spectrum effectiveness and excellent OCP extraction performance on the contaminated soils with different characteristics.

  9. Solidification of spent radioactive organic solvent by sulfoaluminate and Portland cements

    International Nuclear Information System (INIS)

    The solidification of simulated spent radioactive organic solvent, tri-butyl phosphate/kerosene, was investigated by emulsification–solidification method using sulfoaluminate cement (SAC) and Portland cement (PC). Zeolite, calcium hydroxide and MR-1 type emulsifier were mixed into the cement blends for improving the performance of solidified waste forms (SWF). The properties of SWF were evaluated in terms of mechanical strength, leachability and mineral phase analyses. The hydration products of SWF were characterized by X-ray diffraction (XRD). The experimental results showed that the 28 d compressive strengths of SAC solidified waste forms (SACF) and PC solidified waste forms (PCF) were 14.23 and 19.07 MPa, respectively. Leaching sequence of three radionuclides in two kinds of SWF is Cs+ > Sr2+ > Co2+. Compared with PCF, SACF had better performance in preventing nuclides Co2+ and Cs+ from leaching to the environment. The XRD patterns suggested that simulated spent radioactive organic solvent and emulsifier in SWF did not obviously change the hydration products of the two cements (SAC and PC). (author)

  10. Evaluation of the Process of Solvent Vapor Annealing on Organic Thin Films

    KAUST Repository

    Ren, Yi

    2011-07-01

    Solvent vapor annealing has recently emerged as an intriguing, room-temperature, and highly versatile alternative to thermal annealing. The chemically selective interaction between solvents and organic semiconductors opens new opportunities to selectively anneal certain components of the device, while leaving others intact. On the downside, these interactions are complex and rather unpredictable, requiring further investigation. We propose a novel methodology to investigate solvent-film interactions, based on use of an in situ quartz crystal microbalance with dissipation (QCM-D) capability and in situ grazing incidence wide angle X-ray scattering (GIWAXS). These methods make it possible to investigate both qualitatively and quantitatively the solvent vapor uptake, the resulting softening and changes (reversible and/or irreversible) in crystallinity. Using this strategy, we have investigated the solvent vapor annealing of traditional donor and acceptor materials, namely poly(3-hexylthiophene-2,5-diyl) (P3HT) and [6,6]-Phenyl-C61-butyric acid methyl ester (PCBM). We find these materials retain their rigid structure during toluene vapor annealing and do not dewet. We also investigated the toluene vapor annealing of several newly proposed acceptor molecules (pentacene-based) modified with various silyl groups and electron withdrawing groups to tune the packing structure of the acceptor domains and energy levels at the donor-acceptor interface. We found a dramatic effect of the electron-withdrawing group on vapor uptake and whether the film remains rigid, softens, or dissolves completely. In the case of trifluoromethyl electron-withdrawing group, we found the film dissolves, resulting in complete and irreversible loss of long range order. By contrast, the cyano group prevented loss of long range order, instead promoting crystallization in some cases. The silyl groups had a secondary effect in comparison to these. In the last part of the thesis, we investigated the

  11. Recent Advances in Anhydrous Solvents for CO2 Capture: Ionic Liquids, Switchable Solvents, and Nanoparticle Organic Hybrid Materials

    OpenAIRE

    Park, Youngjune; Lin, Kun-Yi Andrew; Park, Ah-Hyung Alissa; Petit, Camille

    2015-01-01

    CO2 capture by amine scrubbing, which has a high CO2 capture capacity and a rapid reaction rate, is the most employed and investigated approach to date. There are a number of recent large-scale demonstrations including the Boundary Dam Carbon Capture Project by SaskPower in Canada that have reported successful implementations of aqueous amine solvent in CO2 capture from flue gases. The findings from these demonstrations will significantly advance the field of CO2 capture in the coming years. ...

  12. Micellization behaviour and thermodynamic parameters of 12-2-12 gemini surfactant in (water + organic solvent) mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Batigoec, Cigdem [Department of Chemistry, Faculty of Sciences, Trakya University, 22030 Edirne (Turkey); Akbas, Halide, E-mail: hakbas34@yahoo.com [Department of Chemistry, Faculty of Sciences, Trakya University, 22030 Edirne (Turkey); Boz, Mesut [Department of Chemistry, Faculty of Sciences, Trakya University, 22030 Edirne (Turkey)

    2011-09-15

    Highlights: > The cmc and {alpha} values of surfactant increased with increasing solvent content and temperature. > The values of ({Delta}G{sub m}{sup 0}) are negative in all cases for the micelle formation becomes less favourable. > The values of negative enthalpy indicate importance of the London dispersion forces for the micellization. > The positive entropy is due to a contribution supplied from the solvent. - Abstract: The effect of organic solvents on micellization behaviour and thermodynamic parameters of a cationic gemini (dimeric) surfactant, C{sub 12}H{sub 25}(CH{sub 3}){sub 2}N{sup +}-(CH{sub 2}){sub 2}-N{sup +}(CH{sub 3}){sub 2}C{sub 12}H{sub 25}.2Br{sup -}, (12-2-12) was studied in aqueous solutions over the range of T = (293.15 to 323.15) K using the conductometric technique. Ethylene glycol (EG), dimethylsulfoxide (DMSO) and 1,4-dioxan (DO) were used as organic solvents with three different contents. The critical micelle concentration (cmc) and the degree of counter ion dissociation ({alpha}) of micelles in the water and in the (water + organic solvent) mixtures including 10%, 20%, and 30% solvent contents were determined. The standard Gibbs free energy ({Delta}G{sub m}{sup 0}), enthalpy ({Delta}H{sub m}{sup 0}) and entropy ({Delta}S{sub m}{sup 0}) of micellization were estimated from the temperature dependence of the cmc values. It was observed that the critical micelle concentration of the gemini surfactant and the degree of counter ion dissociation of the micelle increased as the volume percentage of organic solvent, and temperature increased. The standard Gibbs free energy of micellization was found to be less negative with the increase in the organic solvent content and temperature.

  13. Tryptophanase from Escherichia coli: catalytic and spectral properties in water-organic solvents.

    Science.gov (United States)

    Faleev, N G; Dementieva, I S; Zakomirdina, L N; Gogoleva, O I; Belikov, V M

    1994-08-01

    In water-methanol and water-dimethylformamide (DMF) (1:1 v/v) solutions tryptophanase from E.coli retains its abilities to form a quinonoid complex with quasisubstrates and to catalyze the decomposition of S-o-nitrophenyl-L-cysteine (SOPC). Both the KM and Vmax values decrease in water-organic media. The affinities of tryptophanase for L-alanine, L-tryptophan, oxindolyl-L-alanine and indole in aqueous methanol are decreased, the effect being stronger for the more hydrophobic substances. In a water solution tryptophanase catalizes the reaction of SOPC with indole to form L-tryptophan while in water-organic solvents only decomposition of SOPC is observed.

  14. Preparation and characterization of nonferrous oxide ceramics from metal carboxylates dissolved in organic solvent

    International Nuclear Information System (INIS)

    The solvent extraction system used widely in hydrometallurgy metal-loaded carboxylate extractant was applied to prepare nonferrous oxide powders. When contacted with pure water at temperatures between 130 deg C and 240 deg C, tertiary carboxylate solutions of Ce(lll), Zr(lV), and Cu(ll) were hydrolyzed and precipitated CeO2 ZrO2 and Cu2O respectively. Characterization of the powders demonstrated that these precipitates were crystalline fine particles and were free from contamination by the organic starting material. The extent of precipitation of the oxide products was markedly dependent on process conditions such as temperature and organic phase compositions. For the processing of CeO2 vigorous stirring of the starting solution produced finer particles. (authors)

  15. Brief description and forecast of the array of constants of physical distribution of organic compounds between water and organic solvents with the use of VR parameters scale

    International Nuclear Information System (INIS)

    Statistical processing of the published data file and intrinsic experimental data on the constants of physical distribution of 242 different organic substances between water and 99 organic solvents of different classes in the absence of specific interaction of donor-acceptor character between the substance distributed and solvent was carried out by the OPAG2 program using the US-1055 computer (FORTRAN-4 being the language of programming). It permitted refining and expanding scale of VR (diluent effect) parameters, derived from extraction data

  16. Anaerobic treatment of cellulose bleach plant wastewater: chlorinated organics and genotoxicity removal

    OpenAIRE

    T. R. Chaparro; E. C. Pires

    2011-01-01

    This study assessed the removal efficiency of organic matter and how it relates to the decrease of toxic and mutagenic effects when an anaerobic reactor is used to treat the bleaching effluent from two kraft pulp mills. Parameters such as COD (chemical oxygen demand), DOC (dissolved organic carbon), AOX (adsorbable organic halogen), ASL (acid soluble lignin), color, chlorides, total phenols and absorbance values in the UV-VIS spectral region were measured. The acute and chronic toxicity and g...

  17. (Liquid + liquid) equilibria in ternary aqueous mixtures of phosphoric acid with organic solvents at T = 298.2 K

    Energy Technology Data Exchange (ETDEWEB)

    Ghanadzadeh, H., E-mail: hggilani@guilan.ac.i [Department of Chemistry, Faculty of Science, University of Guilan, Rasht (Iran, Islamic Republic of); Department of Chemical Engineering, University of Guilan, Rasht (Iran, Islamic Republic of); Ghanadzadeh, A., E-mail: aggilani@guilan.ac.i [Department of Chemistry, Faculty of Science, University of Guilan, Rasht (Iran, Islamic Republic of); Aghajani, Z.; Abbasnejad, S.; Shekarsaraee, S. [Department of Chemistry, Faculty of Science, University of Guilan, Rasht (Iran, Islamic Republic of)

    2010-06-15

    (Liquid + liquid) equilibrium (LLE) data for the ternary mixtures of left bracewater (1) + phosphoric acid (2) + organic solvents (3)right brace were determined at T = 298.2 K and atmospheric pressure. The organic solvents were cyclohexane, 2-methyl-2-butanol (tert-amyl alcohol), and isobutyl acetate. All the investigated systems exhibit Type-1 behaviour of LLE. The immiscibility region was found to be larger for the (water + phosphoric acid + cyclohexane) ternary system. The experimental LLE results were correlated with the NRTL model, and the binary interaction parameters were obtained. The reliability of the experimental tie-line results was tested through the Othmer-Tobias and Bachman correlation equations. Distribution coefficients and separation factors were evaluated over the immiscibility regions and a comparison of the extracting capabilities of the solvents was made with respect to these factors. The experimental results indicate the superiority of cyclohexane as the preferred solvent for the extraction of phosphoric acid from its aqueous solutions.

  18. Organic solvent simulations under non-periodic boundary conditions: A library of effective potentials for the GLOB model

    Science.gov (United States)

    Mancini, Giordano; Brancato, Giuseppe; Chandramouli, Balasubramanian; Barone, Vincenzo

    2015-04-01

    We extend the library of solvents that can be treated using the GLOB (general liquid optimized boundary) method, that allows to perform MD simulations under non-periodic boundary conditions (NPBC) optimizing effective potentials between explicit molecules and the boundary for four organic solvents: CHCl3, CCl4, CH3OH and CH3CN. We show that GLOB allows reducing the number of explicit solvent shells to be included, while yielding results comparable with PBC and significant advantages over simulations without explicit boundaries. Finally, we provide polynomial fittings for all available GLOB effective potentials (including SPC water) to simplify their implementation in NPBC MD simulations.

  19. Interim report on testing of off-gas treatment technologies for abatement of atmospheric emissions of chlorinated volatile organic compounds

    Energy Technology Data Exchange (ETDEWEB)

    Haselow, J.S.; Jarosch, T.R.; Rossabi, J.; Burdick, S.; Lombard, K.

    1993-12-01

    The purpose of this report is to briefly summarize the results to date of the off-gas treatment program for atmospheric emissions of chlorinated volatile organic compounds (CVOCs), in particular trichloroethylene (TCE) and perchloroethylene (PCE). This program is part of the Department of Energy`s Office of Technology Development`s Integrated Demonstration for Treatment of Organics in Soil and Water at a Non-Arid Site. The off-gas treatment program was initiated after testing of in-situ air stripping with horizontal wells was completed. That successful test expectedly produced atmospheric emissions of CVOCs that were unabated. It was decided after that test that an off-gas treatment program would complement the Integrated Demonstration not only because off-gas treatment is an integral portion of remediation of CVOC contamination in groundwater and soil but also because several technologies were being developed across the US to mitigate CVOC emissions. A single platform for testing off-gas treatment technologies would facilitate systematic and unbiased evaluation of the emerging technologies.

  20. Interim report on testing of off-gas treatment technologies for abatement of atmospheric emissions of chlorinated volatile organic compounds

    International Nuclear Information System (INIS)

    The purpose of this report is to briefly summarize the results to date of the off-gas treatment program for atmospheric emissions of chlorinated volatile organic compounds (CVOCs), in particular trichloroethylene (TCE) and perchloroethylene (PCE). This program is part of the Department of Energy's Office of Technology Development's Integrated Demonstration for Treatment of Organics in Soil and Water at a Non-Arid Site. The off-gas treatment program was initiated after testing of in-situ air stripping with horizontal wells was completed. That successful test expectedly produced atmospheric emissions of CVOCs that were unabated. It was decided after that test that an off-gas treatment program would complement the Integrated Demonstration not only because off-gas treatment is an integral portion of remediation of CVOC contamination in groundwater and soil but also because several technologies were being developed across the US to mitigate CVOC emissions. A single platform for testing off-gas treatment technologies would facilitate systematic and unbiased evaluation of the emerging technologies

  1. Minimum amount of extracting solvent of AB/BC countercurrent extraction separation using organic feed

    Institute of Scientific and Technical Information of China (English)

    程福祥; 吴声; 张玻; 刘艳; 王嵩龄; 廖春生; 严纯华

    2014-01-01

    For an AB/BC countercurrent extraction separation using organic feed, the conditions to have minimum amount of ex-tracting solvent (Smin) and minimum amount of scrubbing agent solution (Wmin) were discussed, and the formulae of bothSmin and Wmin were deduced. It was shown that only when the ratio of flowrate of central component B leaving aqueous outlet to that leaving organic outlet took a certain optimal value, the AB/BC separation could have Smin as well asWmin, and this optimal ratio was decided by the separation factors between the three components but independent of feed composition.Smin was only relative to the separation factor of A/C pair but regardless of the separation factors of other pairs as well as feed composition, whereasWmin was determined by the separation factors between the components together with feed composition. Meanwhile it was also found that the organic stream out of feed stage was same composition as the initial organic feed when the separation system was given by the two minimum amounts and its steady state was achieved. Finally the results above were used to design a LuYb/YbTm separation case and the stage-wise compositions of each component in both the organic and the aqueous phase at steady state were given by computer simulation.

  2. Influence of Organic Nitrogen Compounds on Chlorine Disinfection%有机氮类化合物对氯消毒影响研究

    Institute of Scientific and Technical Information of China (English)

    徐华; 杨艳玲; 王花平; 梁贞淑

    2012-01-01

    受污染饮用水水源中都含多种有机氮类化合物,会对氯消毒效果产生影响.试验采用有机氮类化合物甘氨酸、亮氨酸、赖氨酸、天冬氨酸、半胱氨酸和甲胺,研究了有机氮类化合物浓度和pH值对消毒效果的影响.结果表明,有机氮类化合物都会和自由氯迅速反应生成大量的有机氯胺,使消毒效果显著下降;不同有机氮类化合物对氯消毒效果的影响有很大差异,半胱氨酸的影响最为明显,使得氯几乎丧失消毒能力.因此,对有机氮类化合物的含量和去除应考虑改善氯的投加方式或氯消毒工艺,建立安全有效的消毒方法.%Many organic nitrogen compounds are contained in polluted resource of drinking water, which seriously influence on chlorine disinfection. Typical organic nitrogen compounds including glycine, leucine, lysine, aspartic acid, cysteine, and methylamine were applied. Influences of organic nitrogen compound dosage and pH on disinfection effects are investigated. Results show that many organic chloramines are produced by prompt action of organic nitrogen compounds and free chlorine to decrease disinfection effects pronounced. Influences on chlorine disinfection effects are different through different organic nitrogen compounds. Influence of cysteine is most obvious to cause chlorine losing disinfection capacity. Therefore, contents and removal of organic nitrogen compounds must be attached. The chlorine dosing mode and chlorine disinfection process can be improved and the effective safe disinfection method must be established.

  3. Towards broadening thermospray flame furnace atomic absorption spectrometry: Influence of organic solvents on the analytical signal of magnesium

    OpenAIRE

    Ezequiel Morzan; Jorge Stripeikis; Mabel Tudino

    2015-01-01

    This study demonstrates the influence of the solvent when thermospray flame furnace atomic absorption spectrometry (TS-FF-AAS) is employed for the determination of elements of low volatility, taking magnesium (Mg) as leading case. Several organic solvents/water solutions of different characteristics (density, surface tension, viscosity, etc.) and proportions were employed for the TS-FF-AAS analytical determination. To this end, solutions containing methanol, ethanol and isopropanol in water w...

  4. Influence of commercially available polyimide and formation conditions on the performance and structure of asymmetric polyimide organic solvent nanofiltration membranes

    OpenAIRE

    Lopes, Mafalda Pessoa

    2009-01-01

    This work covers experimental and theoretical research related to the impact of the polymer structure of commercially available polyimide and polyetherimides as well as the formation conditions on the performance and structure of polyimide Organic Solvent Nanofiltration membranes. The influence in some membrane formation parameters such as polymer choice, solvent system composition, chemical crosslinking, solubility, humidity and coagulation bath temperature on the performance of PI membra...

  5. Physico-chemical properties of Pd nanoparticles produced by Pulsed Laser Ablation in different organic solvents

    International Nuclear Information System (INIS)

    Palladium nanoparticles are arousing an increasing interest because of their strong activity in heterogeneous catalysis in a wide range of reactions. Driven by the interest of producing Pd nanoparticles to be deposited for catalysis over hydrophobic supports, we investigated their synthesis via Pulsed Laser Ablation in Liquid in several organic solvents, as acetone, ethanol, 2-propanol, toluene, n-hexane. The colloids were produced by using a Nd:YAG ns laser and without the addition of surfactant agents. The morphology, composition, stability and oxidation state of the obtained nanoparticles were investigated by TEM-EDS analysis, UV-vis spectroscopy, X-ray Photoelectron Spectroscopy and micro-Raman spectroscopy. The results evidence that the nature of the solvent influences both the yield and the physico-chemical properties of the produced nanoparticles. While in acetone and alcohols spheroidal, non aggregated and stable particles are obtained, in case of toluene and n-hexane few unstable particles surrounded by a gel-like material are produced. Raman/XPS measurements suggest the presence of amorphous or graphitic carbon onto crystalline Pd nanoparticles, which could have hindered their growth and determined the observed smaller sizes if compared to nanoparticles produced in water. The stability of Pd colloids obtained in acetone and alcohols was attributed to adsorbed anions like enolates or alcoholates; non polar solvents like toluene and n-hexane, unable to give rise to adsorbed anionic species, cannot provide any stabilization to the palladium nanoparticles. XPS analyses also evidenced a partial oxidation of particles surface, with a ratio Pd2+:Pd0 of 1:2.5 and 1:4 in acetone and ethanol, respectively.

  6. Physico-chemical properties of Pd nanoparticles produced by Pulsed Laser Ablation in different organic solvents

    Energy Technology Data Exchange (ETDEWEB)

    Cristoforetti, Gabriele, E-mail: gabriele.cristoforetti@cnr.it [National Institute of Optics, Research Area of National Research Council, Via G. Moruzzi 1, 56124 Pisa (Italy); Pitzalis, Emanuela; Spiniello, Roberto [Institute of Chemistry of OrganoMetallic Compounds, Research Area of National Research Council, Via G. Moruzzi 1, 56124 Pisa (Italy); Ishak, Randa [Department of Chem. Eng. And Material Science, University of Pisa, Via Diotisalvi 2, 56126 Pisa (Italy); Giammanco, Francesco [Department of Physics, University of Pisa, Largo B. Pontecorvo 3, 56127 Pisa (Italy); Muniz-Miranda, Maurizio; Caporali, Stefano [Department of Chemistry, University of Florence, Via della Lastruccia 3, 50019 Sesto Fiorentino (Italy)

    2012-01-15

    Palladium nanoparticles are arousing an increasing interest because of their strong activity in heterogeneous catalysis in a wide range of reactions. Driven by the interest of producing Pd nanoparticles to be deposited for catalysis over hydrophobic supports, we investigated their synthesis via Pulsed Laser Ablation in Liquid in several organic solvents, as acetone, ethanol, 2-propanol, toluene, n-hexane. The colloids were produced by using a Nd:YAG ns laser and without the addition of surfactant agents. The morphology, composition, stability and oxidation state of the obtained nanoparticles were investigated by TEM-EDS analysis, UV-vis spectroscopy, X-ray Photoelectron Spectroscopy and micro-Raman spectroscopy. The results evidence that the nature of the solvent influences both the yield and the physico-chemical properties of the produced nanoparticles. While in acetone and alcohols spheroidal, non aggregated and stable particles are obtained, in case of toluene and n-hexane few unstable particles surrounded by a gel-like material are produced. Raman/XPS measurements suggest the presence of amorphous or graphitic carbon onto crystalline Pd nanoparticles, which could have hindered their growth and determined the observed smaller sizes if compared to nanoparticles produced in water. The stability of Pd colloids obtained in acetone and alcohols was attributed to adsorbed anions like enolates or alcoholates; non polar solvents like toluene and n-hexane, unable to give rise to adsorbed anionic species, cannot provide any stabilization to the palladium nanoparticles. XPS analyses also evidenced a partial oxidation of particles surface, with a ratio Pd{sup 2+}:Pd{sup 0} of 1:2.5 and 1:4 in acetone and ethanol, respectively.

  7. Thermodynamic Stability Analysis of Tolbutamide Polymorphs and Solubility in Organic Solvents.

    Science.gov (United States)

    Svärd, Michael; Valavi, Masood; Khamar, Dikshitkumar; Kuhs, Manuel; Rasmuson, Åke C

    2016-06-01

    Melting temperatures and enthalpies of fusion have been determined by differential scanning calorimetry (DSC) for 2 polymorphs of the drug tolbutamide: FI(H) and FV. Heat capacities have been determined by temperature-modulated DSC for 4 polymorphs: FI(L), FI(H), FII, FV, and for the supercooled melt. The enthalpy of fusion of FII at its melting point has been estimated from the enthalpy of transition of FII into FI(H) through a thermodynamic cycle. Calorimetric data have been used to derive a quantitative polymorphic stability relationship between these 4 polymorphs, showing that FII is the stable polymorph below approximately 333 K, above which temperature FI(H) is the stable form up to its melting point. The relative stability of FV is well below the other polymorphs. The previously reported kinetic reversibility of the transformation between FI(L) and FI(H) has been verified using in situ Raman spectroscopy. The solid-liquid solubility of FII has been gravimetrically determined in 5 pure organic solvents (methanol, 1-propanol, ethyl acetate, acetonitrile, and toluene) over the temperature range 278 to 323 K. The ideal solubility has been estimated from calorimetric data, and solution activity coefficients at saturation in the 5 solvents determined. All solutions show positive deviation from Raoult's law, and all van't Hoff plots of solubility data are nonlinear. The solubility in toluene is well below that observed in the other investigated solvents. Solubility data have been correlated and extrapolated to the melting point using a semiempirical regression model. PMID:27238487

  8. Destruction of UST organics and nitrates, polymeric organic wastes, and chlorocarbon solvents by steam reforming

    International Nuclear Information System (INIS)

    In support of the UST, WeDID, VOC/Non-Arid, and VOC/Arid, and VOC/Arid Integrated Demonstrations, organic contaminants and nitrates in Hanford Underground Storage Tank (UST) wastes, polymeric organics in weapon components, and chlorocarbon soil contaminants have been destroyed by exposure to high-temperature steam during bench tests with a quartz reactor and full-scale tests that used the Synthetica Detoxifier, a commercial one-ton-per-day steam reforming waste destruction system. Reactivation of Granular Activated Carbon (GAC) in the Detoxifier and Thermal Gravimetric Analyses (TGA) of the decomposition of sodium nitrate have also been performed

  9. Production of Thermostable Organic Solvent Tolerant Keratinolytic Protease from Thermoactinomyces sp. RM4: IAA Production and Plant Growth Promotion.

    Science.gov (United States)

    Verma, Amit; Singh, Hukum; Anwar, Mohammad S; Kumar, Shailendra; Ansari, Mohammad W; Agrawal, Sanjeev

    2016-01-01

    There are several reports about the optimization of protease production, but only few have optimized the production of organic solvent tolerant keratinolytic proteases that show remarkable exploitation in the development of the non-polluting processes in biotechnological industries. The present study was carried with aim to optimize the production of a thermostable organic solvent tolerant keratinolytic protease Thermoactinomyces sp. RM4 utilizing chicken feathers. Thermoactinomyces sp. RM4 isolated from the soil sample collected from a rice mill wasteyard site near Kashipur, Uttrakhand was identified on the basis of 16S rDNA analysis. The production of organic solvent tolerant keratinolytic protease enzyme by Thermoactinomyces sp. RM4 was optimized by varying physical culture conditions such as pH (10.0), temperature (60°C), inoculum percentage (2%), feather concentration (2%) and agitation rate (2 g) for feather degradation. The result showed that Thermoactinomyces sp. RM4 potentially produces extra-cellular thermostable organic solvent tolerant keratinolytic protease in the culture medium. Further, the feather hydrolysate from keratinase production media showed plant growth promoting activity by producing indole-3-acetic acid itself. The present findings suggest that keratinolytic protease from Thermoactinomyces sp. RM4 offers enormous industrial applications due to its organic solvent tolerant property in peptide synthesis, practical role in feather degradation and potential function in plant growth promoting activity, which might be a superior candidate to keep ecosystem healthy and functional. PMID:27555836

  10. Production of Thermostable Organic Solvent Tolerant Keratinolytic Protease from Thermoactinomyces sp. RM4: IAA Production and Plant Growth Promotion

    Science.gov (United States)

    Verma, Amit; Singh, Hukum; Anwar, Mohammad S.; Kumar, Shailendra; Ansari, Mohammad W.; Agrawal, Sanjeev

    2016-01-01

    There are several reports about the optimization of protease production, but only few have optimized the production of organic solvent tolerant keratinolytic proteases that show remarkable exploitation in the development of the non-polluting processes in biotechnological industries. The present study was carried with aim to optimize the production of a thermostable organic solvent tolerant keratinolytic protease Thermoactinomyces sp. RM4 utilizing chicken feathers. Thermoactinomyces sp. RM4 isolated from the soil sample collected from a rice mill wasteyard site near Kashipur, Uttrakhand was identified on the basis of 16S rDNA analysis. The production of organic solvent tolerant keratinolytic protease enzyme by Thermoactinomyces sp. RM4 was optimized by varying physical culture conditions such as pH (10.0), temperature (60°C), inoculum percentage (2%), feather concentration (2%) and agitation rate (2 g) for feather degradation. The result showed that Thermoactinomyces sp. RM4 potentially produces extra-cellular thermostable organic solvent tolerant keratinolytic protease in the culture medium. Further, the feather hydrolysate from keratinase production media showed plant growth promoting activity by producing indole-3-acetic acid itself. The present findings suggest that keratinolytic protease from Thermoactinomyces sp. RM4 offers enormous industrial applications due to its organic solvent tolerant property in peptide synthesis, practical role in feather degradation and potential function in plant growth promoting activity, which might be a superior candidate to keep ecosystem healthy and functional. PMID:27555836

  11. Anaerobic treatment of cellulose bleach plant wastewater: chlorinated organics and genotoxicity removal

    Directory of Open Access Journals (Sweden)

    T. R. Chaparro

    2011-12-01

    Full Text Available This study assessed the removal efficiency of organic matter and how it relates to the decrease of toxic and mutagenic effects when an anaerobic reactor is used to treat the bleaching effluent from two kraft pulp mills. Parameters such as COD (chemical oxygen demand, DOC (dissolved organic carbon, AOX (adsorbable organic halogen, ASL (acid soluble lignin, color, chlorides, total phenols and absorbance values in the UV-VIS spectral region were measured. The acute and chronic toxicity and genetic toxicity assessments were performed with Daphnia similis, Ceriodaphnia sp. and Allium cepa L, respectively. The removal efficiency of organic matter measured as COD, ranged from 45% to 55%, while AOX removal ranged from 40% to 45%. The acute toxic and chronic effects, as well as the cytotoxic, genotoxic and mutagenic effects, decrease as the biodegradable fraction of the organics is removed. These results, together with the organic load measurement of the effluents of the anaerobic treatment, indicate that these effluents are recalcitrant but not toxic. As expected, color increased when the anaerobic treatment was applied. However, the colored compounds are of microbial origin and do not cause an increase in genotoxic effects. To discharge the wastewater, it is necessary to apply a physico-chemical or aerobic biological post-treatment to the effluents of the anaerobic reactor.

  12. Stabilization of Rocky Flats combustible residues contaminated with plutonium metal and organic solvents

    Energy Technology Data Exchange (ETDEWEB)

    Bowen, S.M.; Cisneros, M.R.; Jacobson, L.L.; Schroeder, N.C.; Ames, R.L.

    1998-09-30

    This report describes tests on a proposed flowsheet designed to stabilize combustible residues that were generated at the Rocky Flats Environmental Technology Site (RFETS) during the machining of plutonium metal. Combustible residues are essentially laboratory trash contaminated with halogenated organic solvents and plutonium metal. The proposed flowsheet, designed by RFETS, follows a glovebox procedure that includes (1) the sorting and shredding of materials, (2) a low temperature thermal desorption of solvents from the combustible materials, (3) an oxidation of plutonium metal with steam, and (4) packaging of the stabilized residues. The role of Los Alamos National Laboratory (LANL) in this study was to determine parameters for the low temperature thermal desorption and steam oxidation steps. Thermal desorption of carbon tetrachloride (CCl{sub 4}) was examined using a heated air stream on a Rocky Flats combustible residue surrogate contaminated with CCl{sub 4}. Three types of plutonium metal were oxidized with steam in a LANL glovebox to determine the effectiveness of this procedure for residue stabilization. The results from these LANL experiments are used to recommend parameters for the proposed RFETS stabilization flowsheet.

  13. Stabilization of Rocky Flats combustible residues contaminated with plutonium metal and organic solvents

    International Nuclear Information System (INIS)

    This report describes tests on a proposed flowsheet designed to stabilize combustible residues that were generated at the Rocky Flats Environmental Technology Site (RFETS) during the machining of plutonium metal. Combustible residues are essentially laboratory trash contaminated with halogenated organic solvents and plutonium metal. The proposed flowsheet, designed by RFETS, follows a glovebox procedure that includes (1) the sorting and shredding of materials, (2) a low temperature thermal desorption of solvents from the combustible materials, (3) an oxidation of plutonium metal with steam, and (4) packaging of the stabilized residues. The role of Los Alamos National Laboratory (LANL) in this study was to determine parameters for the low temperature thermal desorption and steam oxidation steps. Thermal desorption of carbon tetrachloride (CCl4) was examined using a heated air stream on a Rocky Flats combustible residue surrogate contaminated with CCl4. Three types of plutonium metal were oxidized with steam in a LANL glovebox to determine the effectiveness of this procedure for residue stabilization. The results from these LANL experiments are used to recommend parameters for the proposed RFETS stabilization flowsheet

  14. Engymatic synthesis of aspartame precursor in organic solvent; Yuki yobaichu deno asuparutemu zenkutai no koso gosei

    Energy Technology Data Exchange (ETDEWEB)

    Nakanishi, K. [Okayama Univ., Okayama (Japan). Faculty of Engineering

    1996-11-05

    Taking up the synthetic reaction of the precursor of artificial sweetener aspartame for which thermolysin is used as the catalyst, the features and problems of enzymatic reaction in organic solvent are discussed. It is found that immobilized enzyme which has high activity and stability can be prepared by adsorbing high concentration thermolysin in Amberlite XAD7 followed by bridge immobilization. The initial rate of the synthesis and the stability of immobilized enzyme depend on the types of solvents. Continuous reaction is attempted using a columnar ferment reactor (PFR) in ethyl acetate at the beginning, but the yield decreases in a short period because the immobilized enzyme lose its activity gradually from the upper area of the column where Z-Asp concentration is high. When CSTR (complete mixed type reactor) is used, deactivation of immobilized enzyme can be restricted because low Z-Asp concentration in the reactor can be maintained. It is demonstrated that continuous reaction of longer than 200 hours is possible although the reaction rate is as low as 90%. 4 refs., 3 figs., 1 tab.

  15. Parameters Affecting the Synthesis of (Z)-3-hexen-1-yl acetate by Transesterifacation in Organic Solvent

    International Nuclear Information System (INIS)

    (Z)-3-hexen-1-yl esters are important green top-note components of food flavors and fragrances. Crude acetone powders extracted lipases from five plant seedlings of rapeseed, wheat, barley, linseed and maize were investigated for their use in the synthesis of flavor esters with vinyl acetate by transesterification in organic solvents. Rape seedlings showed the highest degree of (Z)-3-hexen-1-yl acetate synthesis with a yield of 76 percentage in 72 h. Rape seedling was chosen as promising biocatalyst to evaluate the effects of some of reaction parameters on (Z)-3-hexen-1-yl acetate synthesis using vinyl acetate and (Z)-3-hexen-1-ol at 40 Degree C in n-hexane with 50 g/L enzyme as catalyst. Acetonitrile proved distinctly superior solvent. The percent remaining activity relative to fresh seedlings powders was highest in wheat and barley. Highest ester yield of 80 percentage was obtained with 0.8 M of substrate concentrations within 48 h. Crude rapeseed lipase afforded a conversion 93 percentage of ethyl alcohol. Higher ester yield was achieved within first 24 h with added molecular. The crude rape seedlings lipase is low cost yet effective, showed potential for the production of green note esters industrially. (author)

  16. Uptake of 10 polar organic solvents during short-term respiration.

    Science.gov (United States)

    Kumagai, S; Oda, H; Matsunaga, I; Kosaka, H; Akasaka, S

    1999-04-01

    Respiratory uptake was investigated for 10 polar organic solvents with high blood/air partition coefficients (lambda(blood/air)): ethyl acetate (lambda(blood/air), 77), methyl iso-butyl ketone (90), methyl acetate (90), methyl propyl ketone (150), acetone (245), iso-pentyl alcohol (381), iso-propyl alcohol (848), methyl alcohol (2590), ethylene glycol monobutyl ether (EGBE, 7970), and propylene glycol monomethyl ether (PGME, 12380). Test-air concentrations (Cinh) were 25 to 200 ppm. Four healthy male volunteers inhaled the test air for 10 min at rest and then room air for 5 min. The percentage of solvent in the end-exhaled air and in the mixed-exhaled air increased after the start of the test-air respiration, and reached a quasi-steady-state level within a few min. The speeds of these increases at the start of the test-air respiration became lower as lambda(blood/air) increased. The mean uptakes (U) for the last five min of the test air respiration were 67.3, 52.9, 60.4, 53.0, 52.6, 63.0, 60.3, 60.8, 79.7, and 81.3%, respectively, for ethyl acetate, methyl iso-butyl ketone, methyl acetate, methyl propyl ketone, acetone, iso-pentyl alcohol, iso-propyl alcohol, methyl alcohol, EGBE and PGME. Thus, U values of the alcohols were higher than those of the ketones and lower than the glycol ethers. The overall view, except for esters, showed that U increased with lambda(water/air) increases. This tendency can be explained by a hypothesis that solvent absorbed in the mucus layer of the respiratory tract is removed by the bronchial blood circulation. U values of ethyl acetate and methyl acetate were higher than those of methyl iso-butyl ketone and methyl propyl ketone, though the lambda(blood/air) values of these esters were nearly equal to those of the ketones. For the respiration of the esters, their metabolites, ethyl alcohol and methyl alcohol, were detected in the exhaled air. The exhalation percentage of the metabolites increased after the start of test-air respiration

  17. Research of component adsorption from the binary mixture of organic solvents

    OpenAIRE

    Карван, Світлана Анатоліївна; Сарібєков, Георгій Савич

    2010-01-01

    Results of superficial tension determinaition of solutions of mixed solvents on the basis of perchloroethylene and 2-propanol are resulted, characteristics of absorption monolayer of their molecules are calculated. Regularities of solvents adsorption by textile materials are investigated.

  18. Kinetic Model of Resin-Catalyzed Decomposition of Acetone Cyanohydrin in Organic Solvent

    Institute of Scientific and Technical Information of China (English)

    章亭洲; 杨立荣; 朱自强; 吴坚平

    2003-01-01

    Decomposition of acetone cyanohydrin is the first-step reaction for preparing (S)-α-cyano-3-phenoxybenzyl alcohol (CPBA) by the one-pot method in organic media. Considering the compatibility of biocatalysts with chemical catalysts and the successive operation in the bioreactor, anion exchange resin (D301) was used as catalyst for this reaction. External diffusion limitation was excluded by raising rotational speed to higher than 190r·min-1 in both solvents. Internal diffusion limitation was verified to be insignificant in this reaction system. The effect of acetone cyanohydrin concentration on the reaction was also investigated. An intrinsic kinetic model was proposed when the mass transfer limitation was excluded, and the average deviation of the model is 10.5%.

  19. Magnetic graphene foam for efficient adsorption of oil and organic solvents.

    Science.gov (United States)

    Yang, Sudong; Chen, Lin; Mu, Lei; Ma, Peng-Cheng

    2014-09-15

    This paper reported the preparation of magnetic graphene foam loaded with magnetite (Fe3O4) nanoparticles and its application for the adsorption of oil and organic solvents. The foam with porous and hierarchical structures was derived from graphene oxide film reduced by gaseous reduction in a hydrothermal system. Drastically different morphologies of Fe3O4 nanoparticles with nanosheet arrays or cubic structures were observed on graphene foam by controlling the reduction degree of graphene oxide under mild conditions. Benefiting from the integration of porous structures and magnetic properties, the graphene foam manifests outstanding oil adsorption capacity, high restoration for absorbates as well as excellent recyclability and stability under cyclic operations. The simple and effective strategy for the preparation of graphene foams developed in this study may offer a new alternative for scale-up production of graphene materials used for the cleanup of oil spills. PMID:24974246

  20. Measurement and correlation of solubility of Tetracycline hydrochloride in six organic solvents

    International Nuclear Information System (INIS)

    Highlights: ► The solubility of Tetracycline hydrochloride (TCH) in six organic solvents was determined. ► Apelblat, NRTL and UNIQUAC models were used to correlate the experimental data. ► Superior correlation was achieved with NRTL model. - Abstract: The solubility of Tetracycline hydrochloride (TCH) in methanol, ethanol, 1-propanol, 1-butanol, acetone, and acetonitrile, was measured using a static method from (283.15 to 318.15) K. The solubility of TCH decreased in the order of methanol, ethanol, 1-propanol, 1-butanol, acetone, and acetonitrile. With increasing temperature, the solubility of TCH increased in ethanol, 1-propanol, 1-butanol, acetone, and acetonitrile but decreased in methanol. Moreover, the experimental solubility data were correlated by the modified Apelblat equation, NRTL and UNIQUAC models, respectively. And the calculated data by NRTL model showed better agreement with experimental values than the modified Apelblat equation and UNIQUAC model.

  1. Molecular Characteristics of Kraft-AQ Pulping Lignin Fractionated by Sequential Organic Solvent Extraction

    Directory of Open Access Journals (Sweden)

    Kun Wang

    2010-08-01

    Full Text Available Kraft-AQ pulping lignin was sequentially fractionated by organic solvent extractions and the molecular properties of each fraction were characterized by chemical degradation, GPC, UV, FT-IR, 13C-NMR and thermal analysis. The average molecular weight and polydispersity of each lignin fraction increased with its hydrogen-bonding capacity (Hildebrand solubility parameter. In addition, the ratio of the non-condensed guaiacyl/syringyl units and the content of β-O-4 linkages increased with the increment of the lignin fractions extracted successively with hexane, diethylether, methylene chloride, methanol, and dioxane. Furthermore, the presence of the condensation reaction products was contributed to the higher thermal stability of the larger molecules.

  2. Lipase-catalyzed Kinetic Resolution of Racemic 1-Trimethylsilylethanol in Organic Solvent

    Institute of Scientific and Technical Information of China (English)

    吴虹; 宗敏华; 王菊芳; 罗涤衡; 娄文勇

    2004-01-01

    The enantioselective esterification of racemic 1-trimethylsilylethanol with acids catalyzed by lipase in organic solvent was successfully performed. The influence of some factors on the reaction was investigated. Among the four lipases explored, Candlda rugosa lipase (CRL) showed the highest activity and enantioselectivity. Octanoic acid was the best acyl donor among the eleven acids studied and n-hexane was the most suitable medium for the reaction. The optimum shaking rate and temperature were found to be 150 r-rain-i and 20~(3 to 30~C, respectively.The enantiomeric excess of the remaining (S)-(-)-1-trimethylsilylethanol was 93% when substrate conversion was 53% upon incubation of the reaction mixture at 30~C, 150 r-rain-i for 12 h.

  3. Solvent effects of a dimethyldicyanoquinonediimine buffer layer as N-type material on the performance of organic photovoltaic cells.

    Science.gov (United States)

    Yang, Eui Yeol; Oh, Se Young

    2014-08-01

    In the present work, we have fabricated organic photovoltaic cells consisting of ITO/PEDOT:PSS/P3HT:PCBM/DMDCNQI/Al using a dip-coating method with various solvent systems. We have investigated solvent effects (such as solubility, viscosity and vapor pressure) in deposition of a thin DMDCNQI buffer layer on the performance of organic photovoltaic cells. The solvent system which had low viscosity and good solubility properties, made a dense and uniform DMDCNQI ultra thin film, resulting in a high performance device. In particular, a prepared organic photovoltaic cell was fabricated using a cosolvent system (methanol:methylenechloride = 3:1) and showed a maximum power conversion efficiency of 4.53%.

  4. Effectiveness of chlorine, organic acids and UV treatments in reducing Escherichia coli O157:H7 and Yersinia enterocolitica on apples.

    Science.gov (United States)

    Escudero, M E; Velázquez, L; Favier, G; de Guzmán, A M

    2003-06-01

    This study assessed the effectiveness of 200 and 500 ppm of chlorine and organic acids (0.5% lactic acid and 0.5% citric acid) in wash solutions, and UV radiation for reducing Escherichia coli O157:H7 and Yersinia enterocolitica on apples contaminated by two different methods. Residual levels of these pathogens after different treatments were compared. On dip inoculated apples, Y. enterocolitica reductions of 2.66 and 2.77 logs were obtained with 200 and 500 ppm chlorine combined with 0.5% lactic acid, respectively. The E. coli O157:H7 population decreased 3.35 log with 0.5% lactic acid wash solution, and 2.72 and 2.62 logs after 500 ppm chlorine and 500 ppm chlorine plus 0.5% lactic acid treatments, respectively. Similar reductions were obtained with UV radiation. On spot inoculated apples, significant (p lactic acid treatment as compared with the control. In sectioned apples, microorganisms infiltrated in inner core region and pulp were not significantly (p lactic acid solution were very proximal to the 5-log score required by FDA for apple disinfection. PMID:12884547

  5. Study on an Organic Hybrid Made from Chlorinated Polyethylene and 2,2'-methylene-bis-(4-methyl-6-cyclohexylphenol)

    Institute of Scientific and Technical Information of China (English)

    刘继涛; 李玮茹; 俞建勇; 王善元

    2003-01-01

    The dynamic mechanical properties and miscibility of an organic hybrid made from chlorinated polyethylene (CPE) and 2, 2'-methylene-bis-(4-methyl-6-cyclohexylphenol) (ZKF) are mainly discussed in this paper. It is found that ZKF acts as an antiplasticizer in CPE matrix and has good miscibility even with large ratio in CPE /ZKF hybrids. The glass transition temperature of various CPE/ZKF hybrids determined by DSC give a good fit to Wood's equation. Bifunctional ZKF is supposed to improve the intermolecular force of CPE, and the improvement is developed when the ZKF content increases. On the other hand, the viscoelastic properties are highly improved with the addition of ZKF. TA and tanδ peak values increase when the ZKF content increase in the CPE /ZKF hybrids, the damping capacity has been improved during the glass transition of CPE /ZKF hybrids. In addition, the glass transition temperature shifts to room temperature from the low temperature with the continuous addition of ZKF to CPE.

  6. Final Report on Testing of Off-Gas Treatment Technologies for Abatement of Atmospheric Emissions of Chlorinated Volatile Organic Compounds

    International Nuclear Information System (INIS)

    The purpose of this report is to summarize the results of the program for off-gas treatment of atmospheric emissions of chlorinated volatile organic compounds (CVOCs), in particular trichloroethylene (TCE) and perchloroethylene (PCE). This program was funded through the Department of Energy Office of Technology Development's VOC's in Non-Arid Soils Integrated Demonstration (VNID). The off-gas treatment program was initiated after testing of in-situ air stripping with horizontal wells was completed (Looney et al., 1991). That successful test expectedly produced atmospheric emissions of CVOCs that were unabated. It was decided after that test that an off-gas treatment is an integral portion of remediation of CVOC contamination in groundwater and soil but also because several technologies were being developed across the United States to mitigate CVOC emissions. A single platform for testing off-gas treatment technologies would facilitate cost effective evaluation of the emerging technologies. Another motivation for the program is that many CVOCs will be regulated under the Clean Air Act Amendments of 1990 and are already regulated by many state regulatory programs. Additionally, compounds such as TCE and PCE are pervasive subsurface environmental contaminants, and, as a result, a small improvement in terms of abatement efficiency or cost will significantly reduce CVOC discharges to the environment as well as costs to United States government and industry

  7. Solvent wash solution

    Science.gov (United States)

    Neace, James C.

    1986-01-01

    Process for removing diluent degradation products from a solvent extraction solution, which has been used to recover uranium and plutonium from spent nuclear fuel. A wash solution and the solvent extraction solution are combined. The wash solution contains (a) water and (b) up to about, and including, 50 volume percent of at least one-polar water-miscible organic solvent based on the total volume of the water and the highly-polar organic solvent. The wash solution also preferably contains at least one inorganic salt. The diluent degradation products dissolve in the highly-polar organic solvent and the organic solvent extraction solvent do not dissolve in the highly-polar organic solvent. The highly-polar organic solvent and the extraction solvent are separated.

  8. Effect of organic solvents on nervous cell membrane as measured by changes in the (Ca2+/Mg2+) ATPase activity and fluidity of synaptosomal membrane.

    Science.gov (United States)

    Edelfors, S; Ravn-Jonsen, A

    1992-03-01

    The effect of various solvents on the central nervous system was studied by using rat brain synaptosomal membranes as an in vitro model. The activity of (Ca2+/Mg2+) ATPase and the membrane fluidity was determined. The alteration of the ATPase activity depended on the physio-chemical characteristics of the solvent in question. Incubation with aliphatic alkanes caused a stimulation of the ATPase activity whereas mixed hydrocarbons as kerosene, white spirit and gasoline inhibited the enzyme. Incubation with chlorinated hydrocarbons caused a biphasic response dependent on the concentration. Oxygen-containing hydrocarbons exhibited various effects as found after incubation with hydrocarbons. The different effects of the solvents on the ATPase activity suggest that the lipophilicity of the solvents is one of more parameters affecting the membrane. Furthermore, the biphasic response following the incubation with chlorinated hydrocarbons indicates that more mechanisms are involved in the enzyme effect. The membrane fluidity is increased with higher concentrations of the solvents. From the results it is concluded that the ATPase activity depends not only on the membrane fluidity and volume, but also on the hydrophilic vicinity of the enzyme molecule. PMID:1533717

  9. Simultaneous treatment of chlorinated organics and removal of metals and radionuclides with bimetals and complexing acids - application to surfactant solutions

    Energy Technology Data Exchange (ETDEWEB)

    Korte, N.E.; Gu, B. [Oak Ridge National Lab., TN (United States)

    1997-10-01

    Currently available methods for separation and treatment of radioactive mixed waste are typically energy-intensive, and often require high temperatures. Passive methods that operate at ambient temperatures are needed. The purpose of this task is to develop bimetallic substrates, using a base metal such as iron and a promoter metal such as palladium (Pd), to provide a passive, low-energy solution to a substantial portion of DOE`s mixed-waste problem. This technology consists of a porous medium that can simultaneously dechlorinate hazardous organics such as TCE and polychlorinated biphenyls (PCBs) at the same time that it removes metallic and hazardous wastes from a solvent/surfactant solution. The porous medium consists of a bimetallic substrate such as palladized iron (Pd/Fe). Palladium is readily chemically plated on iron and preliminary studies suggest that only 0.05 to 0.1% Pd is needed for an efficient reaction. Thus, the cost of the material is reasonable especially is it is long-lived or can be regenerated. Field implementation would consist of the passage of a surfactant-laden, mixed waste through a column or bed of the bimetallic substrate. The organic component of this mixed waste may contain semivolatile compounds such as PCBs or pesticides and herbicides. The bimetal simultaneously removes radionuclides and metals and degrades halogenated hydrocarbons. Virtually any concentration can be treated. Following reaction of the bimetal with the waste stream, the resulting effluent will consist of an uncontaminated aqueous solution of surfactant or solvent that can be reused. The bimetal would then be rinsed with a dilute mineral acid or a mild complexing acid (e.g., oxalic or citric acid) to regenerate the surface and to remove sorbed metals and non-hazardous organic residue. The latter effluent would be low-level radioactive waste in some cases, but it would now be much easier to manage and be of a lower volume than the original mixed waste.

  10. Simultaneous treatment of chlorinated organics and removal of metals and radionuclides with bimetals and complexing acids - application to surfactant solutions

    International Nuclear Information System (INIS)

    Currently available methods for separation and treatment of radioactive mixed waste are typically energy-intensive, and often require high temperatures. Passive methods that operate at ambient temperatures are needed. The purpose of this task is to develop bimetallic substrates, using a base metal such as iron and a promoter metal such as palladium (Pd), to provide a passive, low-energy solution to a substantial portion of DOE's mixed-waste problem. This technology consists of a porous medium that can simultaneously dechlorinate hazardous organics such as TCE and polychlorinated biphenyls (PCBs) at the same time that it removes metallic and hazardous wastes from a solvent/surfactant solution. The porous medium consists of a bimetallic substrate such as palladized iron (Pd/Fe). Palladium is readily chemically plated on iron and preliminary studies suggest that only 0.05 to 0.1% Pd is needed for an efficient reaction. Thus, the cost of the material is reasonable especially is it is long-lived or can be regenerated. Field implementation would consist of the passage of a surfactant-laden, mixed waste through a column or bed of the bimetallic substrate. The organic component of this mixed waste may contain semivolatile compounds such as PCBs or pesticides and herbicides. The bimetal simultaneously removes radionuclides and metals and degrades halogenated hydrocarbons. Virtually any concentration can be treated. Following reaction of the bimetal with the waste stream, the resulting effluent will consist of an uncontaminated aqueous solution of surfactant or solvent that can be reused. The bimetal would then be rinsed with a dilute mineral acid or a mild complexing acid (e.g., oxalic or citric acid) to regenerate the surface and to remove sorbed metals and non-hazardous organic residue. The latter effluent would be low-level radioactive waste in some cases, but it would now be much easier to manage and be of a lower volume than the original mixed waste

  11. Analysis of metabolic pathways by the growth of cells in the presence of organic solvents.

    Science.gov (United States)

    Spinnler, H E; Ginies, C; Khan, J A; Vulfson, E N

    1996-04-16

    A new approach to the analysis of metabolic pathways involving poorly water-soluble intermediates is proposed. It relies upon the ability of the hydrophobic intermediates formed by a sequence of intracellular reactions to cross the membrane(s) and partition between aqueous and organic phases, when cells are incubated in the presence of a nonpolar and nontoxic organic solvent. As a result of this thermodynamically driven efflux of the formed intermediates from the cell, they accumulate in the organic medium in sufficient quantities for GC-MS analysis and identification. This enables direct determination of the sequence of chemical reactions involved with no requirement for the isolation of each individual metabolite from a cell-free extract. The feasibility of the proposed methodology has been demonstrated by the elucidation of the biosynthesis of (R)-gamma-decalactone from (R)-ricinoleic acid catalyzed by the yeast Sporidiobolus ruinenii grown in the presence of decane. The corresponding 4-hydroxy-acid intermediates, formed in the course of beta-oxidation of (R)-ricinoleic acid, were simultaneously observed in a single experiment on the same chromatogram. Potential applications of this proposed methodology are briefly discussed. PMID:11607651

  12. Impact of Chlorine Dioxide Gas Sterilization on Nosocomial Organism Viability in a Hospital Room

    OpenAIRE

    Hewlett, Angela L.; Smith, Philip W.; Gibbs, Shawn G.; Iwen, Peter C.; Lowe, John J.

    2013-01-01

    To evaluate the ability of ClO2 to decontaminate pathogens known to cause healthcare-associated infections in a hospital room strains of Acinetobacter baumannii, Escherichia coli, Enterococcus faecalis, Mycobacterium smegmatis, and Staphylococcus aureus were spot placed in duplicate pairs at 10 sites throughout a hospital room and then exposed to ClO2 gas. Organisms were collected and evaluated for reduction in colony forming units following gas exposure. Six sterilization cycles with varied ...

  13. EXTRACTION OF SEDIMENT-BOUND CHLORINATED ORGANIC COMPOUNDS: IMPLICATIONS ON FATE AND HAZARD ASSESSMENT. (R825513C007)

    Science.gov (United States)

    Five methods were used for the extraction of hexachlorobutadiene and chlorobenzenes from a contaminated estuarine sediment. The following extraction methods were used: Soxhlet extraction, sonication and solvent extraction, sequential solvent extraction, saponification and solv...

  14. First Detection of Non-Chlorinated Organic Molecules Indigenous to a Martian Sample

    Science.gov (United States)

    Freissinet, C.; Glavin, D. P.; Buch, A.; Szopa, C.; Summons, R. E.; Eigenbrode, J. L.; Archer, P. D., Jr.; Brinckerhoff, W. B.; Brunner, A. E.; Cabane, M.; Franz, H. B.; Kashyap, S.; Malespin, C. A.; Martin, M.; Millan, M.; Miller, K.; Navarro-González, R.; Prats, B. D.; Steele, A.; Teinturier, S.; Mahaffy, P. R.

    2016-01-01

    The Sample Analysis at Mars (SAM) instrument onboard Curiosity can perform pyrolysis of martian solid samples, and analyze the volatiles by direct mass spectrometry in evolved gas analysis (EGA) mode, or separate the components in the GCMS mode (coupling the gas chromatograph and the mass spectrometer instruments). In addition, SAM has a wet chemistry laboratory designed for the extraction and identification of complex and refractory organic molecules in the solid samples. The chemical derivatization agent used, N-methyl-N-tert-butyldimethylsilyl- trifluoroacetamide (MTBSTFA), was sealed inside seven Inconel metal cups present in SAM. Although none of these foil-capped derivatization cups have been punctured on Mars for a full wet chemistry experiment, an MTBSTFA leak was detected and the resultant MTBSTFA vapor inside the instrument has been used for a multi-sol MTBSTFA derivatization (MD) procedure instead of direct exposure to MTBSTFA liquid by dropping a solid sample directly into a punctured wet chemistry cup. Pyr-EGA, Pyr-GCMS and Der-GCMS experiments each led to the detection and identification of a variety of organic molecules in diverse formations of Gale Crater.

  15. Environment friendly chemoselective deprotection of acetonides and cleavage of acetals and ketals in aqueous medium without using any catalyst or organic solvent

    Indian Academy of Sciences (India)

    S Mukherjee; A Sengupta; S C Roy

    2013-11-01

    Highly chemoselective environment friendly deprotection of acetonides and cleavage of acetals and ketones has been achieved by heating in aqueous medium without using any catalyst and organic solvent.

  16. Urinary metabolite levels and symptoms in Filipino workers using organic solvents.

    Science.gov (United States)

    Cucueco, M T; Espinosa, N C; Villanueva, M B; Castro, F T; Sison, S Y; Ortega, V S; Hisanaga, N

    1993-01-01

    To compare symptoms with urinary metabolite levels, 900 workers from 7 organic solvent-using industries were studied. Urinary metabolites were determined using a high performance liquid chromatograph. Urinary hippuric acid concentrations exceeding the reference value (2.5 g/g creatinine) were found in 78 (8.7%) workers. However, only 3 (0.3%) and 1 (0.1%) of the participants exceeded the reference value for mandelic (0.8 g/g creatinine) and total methylhippuric acid (1.5 g/g creatinine), respectively. The sum of the values of the ratio of measured urinary metabolite concentration to the corresponding ACGIH's biological exposure indices (BEI) [(HA/BEI of HA + MHA/BEI of MHA + MA/BEI of MA)] exceeded 1.0 in 166 (18.4%) workers. Majority of them were from the footwear manufacturing industry (63/129 or 49.2%). Questionnaire interviews were also administered to determine the prevalence of symptoms while at work (acute symptoms) or within the past 6 months (chronic symptoms). Urinary metabolite levels of individual and mixed solvents were compared with the symptoms of all workers. Analysis using Spearman's rank correlation showed in workers whose urinary hippuric acid exceeded 3.75 g/g creatine (1.5 x BEI), significant correlation between their hippuric acid levels and subjective complaints. Workers whose sum of the values of the ratio of measured urinary metabolite concentration to corresponding BEI exceeded 1.5 were selected and comparing this level with their symptoms, significant correlation was also noted in some complaints. PMID:8406919

  17. Reactions of Organic Ions at Ambient Surfaces in a Solvent-Free Environment

    Science.gov (United States)

    Badu-Tawiah, Abraham K.; Cyriac, Jobin; Cooks, R. Graham

    2012-05-01

    Solvent-free ion/surface chemistry is studied at atmospheric pressure, specifically pyrylium cations, are reacted at ambient surfaces with organic amines to generate pyridinium ions. The dry reagent ions were generated by electrospraying a solution of the organic salt and passing the resulting electrosprayed droplets pneumatically through a heated metal drying tube. The dry ions were then passed through an electric field in air to separate the cations from anions and direct the cations onto a gold substrate coated with an amine. This nontraditional way of manipulating polyatomic ions has provided new chemical insights, for example, the surface reaction involving dry isolated 2,4,6-triphenylpyrylium cations and condensed solid-phase ethanolamine was found to produce the expected N-substituted pyridinium product ion via a pseudobase intermediate in a regiospecific fashion. In solution however, ethanolamine was observed to react through its N-centered and O-centered nucleophilic groups to generate two isomeric products via 2H-pyran intermediates. The O-centered nucleophile reacted less rapidly to give the minor product. The surface reaction product was characterized in situ by surface enhanced Raman spectroscopy, and ex situ using mass spectrometry and H/D exchange, and found to be chemically the same as the major pyridinium solution-phase reaction product.

  18. PEGylation of G-CSF in organic solvent markedly increase the efficacy and reactivity through protein unfolding, hydrolysis inhibition and solvent effect.

    Science.gov (United States)

    Peng, Fei; Liu, Yongdong; Li, Xiunan; Sun, Lijing; Zhao, Dawei; Wang, Qingqing; Ma, Guanghui; Su, Zhiguo

    2014-01-20

    Previous studies demonstrated that hydrophobic proteins could be PEGylated in organic phase rather than water phase. It is still not known what the difference is for a hydrophilic protein's PEGylation in these two different phases. In this study, granulocyte colony stimulating factor (G-CSF) was dissolved in neat dimethyl sulfoxide (DMSO) and was PEGylated. In comparison with the PEGylation in water solution, the PEGylation degree in the organic solvent increased by 33% and 42% for PEG-maleimide (MAL-PEG) and PEG-succinimidyl carbonate (SC-PEG) respectively. Structure analysis revealed that the protein was unfolded in DMSO, which could make the PEGylated sites of G-CSF easily accessible. The hydrolysis half-life in water solution was 40min and 9h for SC-PEG and MAL-PEG respectively. However, in DMSO solvent, PEGs were very stable and no hydrolysis could be detected. Stopped-flow demonstrated that the conjugation speed of G-CSF by MAL-PEG and SC-PEG in DMSO were 1.6×10(4) and 2×10(2) times faster than those in aqueous solution. The remarkable acceleration could mainly be attributed to an increase of protein nucleophilicity in DMSO. The results of this study could be referential to industrial application where the cost of PEG reagents and the speed of reaction on large scale are very important. PMID:24315970

  19. Improved Cellulose and Organic-Solvents based Lignocellulosic Fractionation Pre-treatment of Organic Waste for Bioethanol Production

    Directory of Open Access Journals (Sweden)

    Valeriy Bekmuradov

    2014-06-01

    Full Text Available This study investigates the performance of the Cellulose and Organic-Solvents based Lignocellulosic Fractionation (COSLIF method for the pretreatment of Source-Separated Organic (SSO waste. An improvement on the standard method of COSLIF pre-treatment was developed based on lower enzyme loading and using an ethanol washing instead of acetone. It was demonstrated that a much higher glucose yield (90% after 72 hours was possible with this improvement, as compared to the original method, which yielded 70% in the same time frame. Evaluation of the enzymatic hydrolysate obtained from the modified COSLIF pretreatment was further examined by anaerobic fermentation with Zymomonas mobilis 8b strain. At 48 hours, ethanol concentration reached to 140 g/L, which is equivalent to 0.48 g of ethanol produced per gram of SSO biomass. This study demonstrated that the modified COSLIF pretreatment provides a substantial improvement over the standard method in terms of enzyme savings, glucose formation, and ethanol production.

  20. Highly efficient synthesis of endomorphin-2 under thermodynamic control catalyzed by organic solvent stable proteases with in situ product removal.

    Science.gov (United States)

    Xu, Jiaxing; Sun, Honglin; He, Xuejun; Bai, Zhongzhong; He, Bingfang

    2013-02-01

    An efficient enzymatic synthesis of endomorphin-2 (EM-2) was achieved using organic solvent stable proteases in nonaqeous media, based on thermodynamic control and an in situ product removal methodology. The high stability of biocatalysts in organic solvents enabled the aleatoric modulation of the nonaqueous reaction media to shift thermodynamic equilibrium toward synthesis. Peptide Boc-Phe-Phe-NH2 was synthesized with a high yield of 96% by the solvent stable protease WQ9-2 in monophase medium with an economical molar ratio of the substrate of 1:1. The tetrapeptide Boc-Tyr-Pro-Phe-Phe-NH2 was synthesized with a yield of 88% by another organic solvent tolerant protease PT121 from Boc-Tyr-Pro-OH and Phe-Phe-NH2 in an organic-aqueous biphasic system. The reaction-separation coupling in both enzymatic processes provides "driving forces" for the synthetic reactions and gives a high yield and high productivity without purification of the intermediate, thereby making the synthesis more amenable to scale-up. PMID:23305895

  1. Highly efficient synthesis of endomorphin-2 under thermodynamic control catalyzed by organic solvent stable proteases with in situ product removal.

    Science.gov (United States)

    Xu, Jiaxing; Sun, Honglin; He, Xuejun; Bai, Zhongzhong; He, Bingfang

    2013-02-01

    An efficient enzymatic synthesis of endomorphin-2 (EM-2) was achieved using organic solvent stable proteases in nonaqeous media, based on thermodynamic control and an in situ product removal methodology. The high stability of biocatalysts in organic solvents enabled the aleatoric modulation of the nonaqueous reaction media to shift thermodynamic equilibrium toward synthesis. Peptide Boc-Phe-Phe-NH2 was synthesized with a high yield of 96% by the solvent stable protease WQ9-2 in monophase medium with an economical molar ratio of the substrate of 1:1. The tetrapeptide Boc-Tyr-Pro-Phe-Phe-NH2 was synthesized with a yield of 88% by another organic solvent tolerant protease PT121 from Boc-Tyr-Pro-OH and Phe-Phe-NH2 in an organic-aqueous biphasic system. The reaction-separation coupling in both enzymatic processes provides "driving forces" for the synthetic reactions and gives a high yield and high productivity without purification of the intermediate, thereby making the synthesis more amenable to scale-up.

  2. 40 CFR 63.5753 - How do I calculate the combined organic HAP content of aluminum wipedown solvents and aluminum...

    Science.gov (United States)

    2010-07-01

    ... HAP content of aluminum wipedown solvents and aluminum recreational boat surface coatings? 63.5753... Standards for Hazardous Air Pollutants for Boat Manufacturing Standards for Aluminum Recreational Boat Surface Coating Operations § 63.5753 How do I calculate the combined organic HAP content of...

  3. 40 CFR Table 4 to Subpart Pppp of... - Default Organic HAP Mass Fraction for Petroleum Solvent Groups a

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 12 2010-07-01 2010-07-01 true Default Organic HAP Mass Fraction for Petroleum Solvent Groups a 4 Table 4 to Subpart PPPP of Part 63 Protection of Environment ENVIRONMENTAL... of Plastic Parts and Products Pt. 63, Subpt. PPPP, Table 4 Table 4 to Subpart PPPP of Part...

  4. Organic solvent wetting properties of UV and plasma treated ZnO nanorods: printed electronics approach

    KAUST Repository

    Sliz, Rafal

    2012-09-13

    Due to low manufacturing costs, printed organic solar cells are on the short-list of renewable and environmentally- friendly energy production technologies of the future. However, electrode materials and each photoactive layer require different techniques and approaches. Printing technologies have attracted considerable attention for organic electronics due to their potentially high volume and low cost processing. A case in point is the interface between the substrate and solution (ink) drop, which is a particularly critical issue for printing quality. In addition, methods such as UV, oxygen and argon plasma treatments have proven suitable to increasing the hydrophilicity of treated surfaces. Among several methods of measuring the ink-substrate interface, the simplest and most reliable is the contact angle method. In terms of nanoscale device applications, zinc oxide (ZnO) has gained popularity, owing to its physical and chemical properties. In particular, there is a growing interest in exploiting the unique properties that the so-called nanorod structure exhibits for future 1-dimensional opto-electronic devices. Applications, such as photodiodes, thin-film transistors, sensors and photo anodes in photovoltaic cells have already been demonstrated. This paper presents the wettability properties of ZnO nanorods treated with UV illumination, oxygen and argon plasma for various periods of time. Since this work concentrates on solar cell applications, four of the most common solutions used in organic solar cell manufacture were tested: P3HT:PCBM DCB, P3HT:PCBM CHB, PEDOT:PSS and water. The achieved results prove that different treatments change the contact angle differently. Moreover, solvent behaviour varied uniquely with the applied treatment. © (2012) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.

  5. Nickel-Catalyzed Suzuki–Miyaura Cross-Coupling in a Green Alcohol Solvent for an Undergraduate Organic Chemistry Laboratory

    Science.gov (United States)

    2015-01-01

    A modern undergraduate organic chemistry laboratory experiment involving the Suzuki–Miyaura coupling is reported. Although Suzuki–Miyaura couplings typically employ palladium catalysts in environmentally harmful solvents, this experiment features the use of inexpensive nickel catalysis, in addition to a “green” alcohol solvent. The experiment employs heterocyclic substrates, which are important pharmaceutical building blocks. Thus, this laboratory procedure exposes students to a variety of contemporary topics in organic chemistry, including transition metal-catalyzed cross-couplings, green chemistry, and the importance of heterocycles in drug discovery, none of which are well represented in typical undergraduate organic chemistry curricula. The experimental protocol uses commercially available reagents and is useful in both organic and inorganic instructional laboratories. PMID:25774064

  6. Characterisation of solvent extractable organic constituents in atmospheric particulate matter: an overview

    Directory of Open Access Journals (Sweden)

    Célia A. Alves

    2008-03-01

    Full Text Available In spite of accounting for 10-70% of the atmospheric aerosol mass, particulate-phase organic compounds are not well characterised, and many aspects of aerosol formation and evolution are still unknown. The growing awareness of the impact of particulate aerosols on climate, and the incompletely recognised but serious effects of anthropogenic constituents on air quality and human health, have conducted to several scientific studies. These investigations have provided information about the behaviour of atmospheric particulate matter and the description of the character of its carbonaceous content. The compilation of such results is important as they append to the emergent global-wide dataset of the organic composition of atmospheric aerosols. The contribution of the major emission sources to regional particulate pollution can be diagnosed by using specific molecular markers. This overview is mainly focused on results obtained with gas chromatography coupled with mass spectrometry, since it is the analytical method of choice in elucidating the solvent-extractable organic compounds in atmospheric particulate matter. A synopsis of the selection of organic tracers and the application of geochemical parameters to the analysis of organic constituents as a tool for source apportionment is shown here. Besides the assessment of current knowledge, this paper also presents the identification of further areas of concern.Apesar de constituirem 10-70% da massa do aerosol atmosférico, a caracterização dos compostos orgânicos particulados permanece ainda deficitária e vários aspectos relativos à formação e evolução do aerossol são ainda desconhecidos. A crescente preocupação com o impacto do aerosol particulado no clima e os reconhecidos efeitos dos constituintes antropogênicos na qualidade do ar e na saúde humana têm motivado a realização de numerosos estudos. Estas investigações têm fornecido informações relevantes sobre o comportamento

  7. Solvent Vapor Treatment Effects on Poly(3-hexylthiophene Thin Films and its Application for Interpenetrating Heterojunction Organic Solar Cells

    Directory of Open Access Journals (Sweden)

    Masanori Ozaki

    2010-11-01

    Full Text Available The solvent vapor treatment (SVT for poly(3-hexylthiophene (PAT6 films and its application to interpenetrating heterojunction organic solar cells have been studied. It was found that SVT could improve the crystallinity and electrical characteristics of the PAT6 films. We fabricated organic solar cells with an interpenetrating structure of PAT6 and fullerenes utilizing the SVT process, and discuss the improved performance of the solar cells by taking the film crystallinity, optical properties, and morphology into consideration.

  8. Project Summary. IN-SITU AQUIFER RESTORATION OF CHLORINATED ALIPHATICS BY METHANOTROPHIC BACTERIA

    Science.gov (United States)

    This project evaluated the potential of an innovative approach to aquifer restoration: enhanced in-situ biotransformation of chlorinated aliphatic solvents by a bacterial community grown on methane under aerobic conditions. The target chlorinated compounds were trichloroethene (...

  9. Use of volatile organic solvents in headspace liquid-phase microextraction by direct cooling of the organic drop using a simple cooling capsule.

    Science.gov (United States)

    Ghiasvand, Ali Reza; Yazdankhah, Fatemeh; Hajipour, Somayeh

    2016-08-01

    A low-cost and simple cooling-assisted headspace liquid-phase microextraction device for the extraction and determination of 2,6,6-trimethyl-1,3 cyclohexadiene-1-carboxaldehyde (safranal) in Saffron samples, using volatile organic solvents, was fabricated and evaluated. The main part of the cooling-assisted headspace liquid-phase microextraction system was a cooling capsule, with a Teflon microcup to hold the extracting organic solvent, which is able to directly cool down the extraction phase while the sample matrix is simultaneously heated. Different experimental factors such as type of organic extraction solvent, sample temperature, extraction solvent temperature, and extraction time were optimized. The optimal conditions were obtained as: extraction solvent, methanol (10 μL); extraction temperature, 60°C; extraction solvent temperature, 0°C; and extraction time, 20 min. Good linearity of the calibration curve (R(2) = 0.995) was obtained in the concentration range of 0.01-50.0 μg/mL. The limit of detection was 0.001 μg/mL. The relative standard deviation for 1.0 μg/mL of safranal was 10.7% (n = 6). The proposed cooling-assisted headspace liquid-phase microextraction device was coupled (off-line) to high-performance liquid chromatography and used for the determination of safranal in Saffron samples. Reasonable agreement was observed between the results of the cooling-assisted headspace liquid-phase microextraction high-performance liquid chromatography method and those obtained by a validated ultrasound-assisted solvent extraction procedure. PMID:27311349

  10. Thin-film composite crosslinked polythiosemicarbazide membranes for organic solvent nanofiltration (OSN)

    KAUST Repository

    Aburabie, Jamaliah

    2015-01-01

    In this work we report a new class of solvent stable thin-film composite (TFC) membrane fabricated on crosslinked polythiosemicarbazide (PTSC) as substrate that exhibits superior stability compared with other solvent stable polymeric membranes reported up to now. Integrally skinned asymmetric PTSC membranes were prepared by the phase inversion process and crosslinked with an aromatic bifunctional crosslinker to improve the solvent stability. TFC membranes were obtained via interfacial polymerization using trimesoyl chloride (TMC) and diaminopiperazine (DAP) monomers. The membranes were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and contact angle measurement.The membranes exhibited high fluxes toward solvents like tetrahydrofuran (THF), dimethylformamide (DMF) and dimethylsulfoxide (DMSO) ranging around 20L/m2 h at 5bar with a molecular weight cut off (MWCO) of around 1000g/mol. The PTSC-based thin-film composite membranes are very stable toward polar aprotic solvents and they have potential applications in the petrochemical and pharmaceutical industry.

  11. Microwave activation of electrochemical processes: enhanced electrodehalogenation in organic solvent media.

    Science.gov (United States)

    Tsai, Yu-Chen; Coles, Barry A; Compton, Richard G; Marken, Frank

    2002-08-21

    The effect of high-intensity microwave radiation focused into a "hot spot" region in the vicinity of an electrode on electrochemical processes with and without coupled chemical reaction steps has been investigated in organic solvent media. First, the electrochemically reversible oxidation of ferrocene in acetonitrile and DMF is shown to be affected by microwave-induced thermal activation, resulting in increased currents and voltammetric wave shape effects. A FIDAP simulation investigation allows quantitative insight into the temperature distribution and concentration gradients at the electrode / solution interface. Next, the effect of intense microwave radiation on electroorganic reactions is considered for the case of ECE processes. Experimental data for the reduction of p-bromonitrobenzene, o-bromonitrobenzene, and m-iodonitrobenzene in DMF and acetonitrile are analyzed in terms of an electron transfer (E), followed by a chemical dehalogenation step (C), and finally followed by another electron-transfer step (E). The presence of the "hot spot" in the solution phase favors processes with high activation barriers.

  12. Bacterial assisted degradation of chlorpyrifos: The key role of environmental conditions, trace metals and organic solvents.

    Science.gov (United States)

    Khalid, Saira; Hashmi, Imran; Khan, Sher Jamal

    2016-03-01

    Wastewater from pesticide industries, agricultural or surface runoff containing pesticides and their residues has adverse environmental impacts. Present study demonstrates effect of petrochemicals and trace metals on chlorpyrifos (CP) biotransformation often released in wastewater of agrochemical industry. Biodegradation was investigated using bacterial strain Pseudomonas kilonensis SRK1 isolated from wastewater spiked with CP. Optimal environmental conditions for CP removal were CFU (306 × 10(6)), pH (8); initial CP concentration (150 mg/L) and glucose as additional carbon source. Among various organic solvents (petrochemicals) used in this study toluene has stimulatory effect on CP degradation process using SRK1, contrary to this benzene and phenol negatively inhibited degradation process. Application of metal ions (Cu (II), Fe (II) Zn (II) at low concentration (1 mg/L) took part in biochemical reaction and positively stimulated CP degradation process. Metal ions at high concentrations have inhibitory effect on degradation process. A first order growth model was shown to fit the data. It could be concluded that both type and concentration of metal ions and petrochemicals can affect CP degradation process. PMID:26692411

  13. Bacterial assisted degradation of chlorpyrifos: The key role of environmental conditions, trace metals and organic solvents.

    Science.gov (United States)

    Khalid, Saira; Hashmi, Imran; Khan, Sher Jamal

    2016-03-01

    Wastewater from pesticide industries, agricultural or surface runoff containing pesticides and their residues has adverse environmental impacts. Present study demonstrates effect of petrochemicals and trace metals on chlorpyrifos (CP) biotransformation often released in wastewater of agrochemical industry. Biodegradation was investigated using bacterial strain Pseudomonas kilonensis SRK1 isolated from wastewater spiked with CP. Optimal environmental conditions for CP removal were CFU (306 × 10(6)), pH (8); initial CP concentration (150 mg/L) and glucose as additional carbon source. Among various organic solvents (petrochemicals) used in this study toluene has stimulatory effect on CP degradation process using SRK1, contrary to this benzene and phenol negatively inhibited degradation process. Application of metal ions (Cu (II), Fe (II) Zn (II) at low concentration (1 mg/L) took part in biochemical reaction and positively stimulated CP degradation process. Metal ions at high concentrations have inhibitory effect on degradation process. A first order growth model was shown to fit the data. It could be concluded that both type and concentration of metal ions and petrochemicals can affect CP degradation process.

  14. In-Vitro Characterization and Oral Bioavailability of Organic Solvent-free Solid Dispersions Containing Telmisartan.

    Science.gov (United States)

    Cao, Yue; Shi, Li-Li; Cao, Qing-Ri; Yang, Mingshi; Cui, Jing-Hao

    2016-01-01

    Poorly water-soluble drugs often suffer from limited or irreproducible clinical response due to their low solubility and dissolution rate. In this study, organic solvent-free solid dispersions (OSF-SDs) containing telmisartan (TEL) were prepared using polyvinylpyrrolidone K30 (PVP K30) and polyethylene glycol 6000 (PEG 6000) as hydrophilic polymers, sodium hydroxide (NaOH) as an alkalizer, and poloxamer 188 as a surfactant by a lyophilization method. In-vitro dissolution rate and physicochemical properties of the OSF-SDs were characterized using the USP I basket method, differential scanning calorimetry (DSC), X-ray diffractometry (XRD) and fourier transform-infrared (FT-IR) spectroscopy. In addition, the oral bioavailability of OSF-SDs in rats was evaluated by using TEL bulk powder as a reference. The dissolution rates of the OSF-SDs were significantly enhanced as compared to TEL bulk powder. The results from DSC, XRD showed that TEL was molecularly dispersed in the OSF-SDs as an amorphous form. The FT-IR results suggested that intermolecular hydrogen bonding had formed between TEL and its carriers. The OSF-SDs exhibited significantly higher AUC0-24 h and Cmax, but similar Tmax as compared to the reference. This study demonstrated that OSF-SDs can be a promising method to enhance the dissolution rate and oral bioavailability of TEL. PMID:27642309

  15. Molecular cloning of a novel bioH gene from an environmental metagenome encoding a carboxylesterase with exceptional tolerance to organic solvents

    DEFF Research Database (Denmark)

    Shi, Yuping; Pan, Yingjie; Li, Bailin;

    2013-01-01

    Hx with other known BioH proteins revealed interesting diversity in their sensitivity to ionic and nonionic detergents and organic solvents, and BioHx exhibited exceptional resistance to organic solvents, being the most tolerant one amongst all known BioH enzymes. This ascribed BioHx as a novel carboxylesterase...

  16. Long-term occupational exposure to organic solvents affects color vision, contrast sensitivity and visual fields.

    Directory of Open Access Journals (Sweden)

    Thiago Leiros Costa

    Full Text Available The purpose of this study was to evaluate the visual outcome of chronic occupational exposure to a mixture of organic solvents by measuring color discrimination, achromatic contrast sensitivity and visual fields in a group of gas station workers. We tested 25 workers (20 males and 25 controls with no history of chronic exposure to solvents (10 males. All participants had normal ophthalmologic exams. Subjects had worked in gas stations on an average of 9.6 ± 6.2 years. Color vision was evaluated with the Lanthony D15d and Cambridge Colour Test (CCT. Visual field assessment consisted of white-on-white 24-2 automatic perimetry (Humphrey II-750i. Contrast sensitivity was measured for sinusoidal gratings of 0.2, 0.5, 1.0, 2.0, 5.0, 10.0 and 20.0 cycles per degree (cpd. Results from both groups were compared using the Mann-Whitney U test. The number of errors in the D15d was higher for workers relative to controls (p<0.01. Their CCT color discrimination thresholds were elevated compared to the control group along the protan, deutan and tritan confusion axes (p<0.01, and their ellipse area and ellipticity were higher (p<0.01. Genetic analysis of subjects with very elevated color discrimination thresholds excluded congenital causes for the visual losses. Automated perimetry thresholds showed elevation in the 9°, 15° and 21° of eccentricity (p<0.01 and in MD and PSD indexes (p<0.01. Contrast sensitivity losses were found for all spatial frequencies measured (p<0.01 except for 0.5 cpd. Significant correlation was found between previous working years and deutan axis thresholds (rho = 0.59; p<0.05, indexes of the Lanthony D15d (rho=0.52; p<0.05, perimetry results in the fovea (rho= -0.51; p<0.05 and at 3, 9 and 15 degrees of eccentricity (rho= -0.46; p<0.05. Extensive and diffuse visual changes were found, suggesting that specific occupational limits should be created.

  17. Controlled Burning of Forest Detritus Altering Spectroscopic Characteristics and Chlorine Reactivity of Dissolved Organic Matter: Effects of Temperature and Oxygen Availability.

    Science.gov (United States)

    Wang, Jun-Jian; Dahlgren, Randy A; Chow, Alex T

    2015-12-15

    Forest fires occur with increasing frequency and severity in the western United States, potentially altering the chemistry and quantity of dissolved organic matter (DOM) and disinfection byproduct (DBP) precursors exported from forested watersheds. However, little is known concerning effects of the fire triangle (heat, oxygen, and fuel) on DOM alteration. Using detritus from Pinus ponderosa and Abies concolor (dominant species in forests in the western United States), we prepared DOM from unburned and burned detritus under hypoxic (pyrolysis) and oxic conditions (thermal oxidation) at 250 and 400 °C. DOM characteristics and chlorine reactivity were evaluated by absorption and fluorescence spectroscopy and chlorination-based DBP formation potential tests. Spectroscopic results suggest that burned-detritus extracts had lower molecular weight (reflected by increased E2:E3 and fluorescence index) and divergent aromaticity (reflected by SUVA254) depending on oxygen availability. Temperature and oxygen availability interacted to alter the chlorine reactivity of fire-affected DOM. Increasing temperature from 50 to 400 °C resulted in decreased reactivities for trihalomethane and chloral hydrate formation and divergent reactivities for haloacetonitrile formation (unchanged for pyrolysis and increased for oxidation) and haloketone formation (increased for pyrolysis and decreased for oxidation). We demonstrate that DBP precursors in fire-affected forest detritus are highly dependent on temperature and oxygen availability. PMID:26496434

  18. NMR Chemical Shift Ranges of Urine Metabolites in Various Organic Solvents

    Science.gov (United States)

    Görling, Benjamin; Bräse, Stefan; Luy, Burkhard

    2016-01-01

    Signal stability is essential for reliable multivariate data analysis. Urine samples show strong variance in signal positions due to inter patient differences. Here we study the exchange of the solvent of a defined urine matrix and how it affects signal and integral stability of the urinary metabolites by NMR spectroscopy. The exchange solvents were methanol, acetonitrile, dimethyl sulfoxide, chloroform, acetone, dichloromethane, and dimethyl formamide. Some of these solvents showed promising results with a single batch of urine. To evaluate further differences between urine samples, various acid, base, and salt solutions were added in a defined way mimicking to some extent inter human differences. Corresponding chemical shift changes were monitored. PMID:27598217

  19. NMR Chemical Shift Ranges of Urine Metabolites in Various Organic Solvents

    Directory of Open Access Journals (Sweden)

    Benjamin Görling

    2016-09-01

    Full Text Available Signal stability is essential for reliable multivariate data analysis. Urine samples show strong variance in signal positions due to inter patient differences. Here we study the exchange of the solvent of a defined urine matrix and how it affects signal and integral stability of the urinary metabolites by NMR spectroscopy. The exchange solvents were methanol, acetonitrile, dimethyl sulfoxide, chloroform, acetone, dichloromethane, and dimethyl formamide. Some of these solvents showed promising results with a single batch of urine. To evaluate further differences between urine samples, various acid, base, and salt solutions were added in a defined way mimicking to some extent inter human differences. Corresponding chemical shift changes were monitored.

  20. NMR Chemical Shift Ranges of Urine Metabolites in Various Organic Solvents.

    Science.gov (United States)

    Görling, Benjamin; Bräse, Stefan; Luy, Burkhard

    2016-01-01

    Signal stability is essential for reliable multivariate data analysis. Urine samples show strong variance in signal positions due to inter patient differences. Here we study the exchange of the solvent of a defined urine matrix and how it affects signal and integral stability of the urinary metabolites by NMR spectroscopy. The exchange solvents were methanol, acetonitrile, dimethyl sulfoxide, chloroform, acetone, dichloromethane, and dimethyl formamide. Some of these solvents showed promising results with a single batch of urine. To evaluate further differences between urine samples, various acid, base, and salt solutions were added in a defined way mimicking to some extent inter human differences. Corresponding chemical shift changes were monitored. PMID:27598217

  1. Formation of chlorinated organic compounds in fluidized bed combustion of recycled fuels; Kloorattujen orgaanisten yhdisteiden muodostuminen kierraetyspolttoaineiden leijukerrospoltossa

    Energy Technology Data Exchange (ETDEWEB)

    Vesterinen, R.; Kallio, M.; Kirjalainen, T.; Kolsi, A.; Merta, M. [VTT Energy, Jyvaeskylae (Finland)

    1997-10-01

    Four tests of co-combustion of recycled fuels (REP) with peat and coal in the 15 kW fluidized bed reactor were performed. The recycled fuel was so-called dry fraction in four vessels sampling at Keltinmaeki. In three tests a part of peat energy was replaced with coal. The mixtures were prepared so that in all mixtures 25 % of energy was recycled fuel and 75 % was either peat or the mixture of peat and coal. The concentrations of polyaromatic hydrocarbons (PAH), polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs) and chlorophenols decreased with increasing part of coal due to the increasing sulphur/chlorine ratio. Principal Component Analysis (PCA) and Partial Least Square regression analysis (PLS) showed that the chlorine, copper and sulphur contents of the fuel effected most on the concentrations of chlorophenols, chlorobenzenes, PCBs and PCDDs/PCDFs. Other variables influencing on a model were the lead concentration and the sulphur/chlorine ratio in fuel and the hydrogen chloride concentration of the flue gas. The concentrations of chlorophenols and chlorobenzenes were also significant for PCDD/PCDF concentrations in flue gas. The sulphur, chlorine, copper and chromium contents in fly ash and the temperature of the reactor influenced on the chlorophenol, chlorobenzene, PCB and PCDD/PCDF concentrations in fly ash. The chlorophenol and chlorobenzene contents in fly ash, the sulphur/chlorine ratio and the lead content in fuel, the sulphur dioxide, hydrogen chloride and carbon monoxide concentrations in flue gas had also influence on PCDD/PCDF concentrations in fly ash

  2. The effect of organic solvent, temperature and mixing time on the production of oil from Moringa oleifera seeds

    Science.gov (United States)

    Ghazali, Q.; Yasin, N. H. M.

    2016-06-01

    The effect of three different organic solvent, temperature and mixing time on the production of oil from M.oleifera seeds were studied to evaluate the effectiveness in obtaining the high oil yield based on the percentage of oil production. The modified version of Soxhlet extraction method was carried out to extract the oil from M.oleifera seeds by using hexane, heptane and ethanol as the organic solvent. Among the three solvents, it is found that heptane yield higher oil from M.oleifera seeds with maximum oil yield of 36.37% was obtained followed by hexane and ethanol with 33.89% and 18.46%, respectively. By using heptane as a solvent, the temperature (60oC, 70oC, 80oC) and mixing time (6 h, 7 h, and 8 h) were investigated to ensure the high oil yield over the experimental ranges employed and high oil yield was obtained at 600C for 6 h with percentage oil yield of 36.37%. The fatty acid compositions of M.oleifera seeds oil were analyzed using Gas Chromatography/Mass Spectrometry (GC-MS). The main components of fatty acid contained in the oil extracted from M.oleifera seeds was oleic acid, followed by palmitic acid and arachidic acid, and small amount of behenic acid and margaric acid.

  3. GREENER REACTIONS UNDER SOLVENT FREE CONDITIONS

    Directory of Open Access Journals (Sweden)

    Hiren M. Marvaniya

    2011-06-01

    Full Text Available The toxicity and volatile nature of many organic solvents, particularly chlorinated hydrocarbons that are widely used in huge amounts for organic reactions have posed a serious threat to the environment. Thus, design of solventless catalytic reaction has received tremendous attention in recent times in the area of green synthesis. A solvent-free or solid state reaction may be carried out using the reactants alone or incorporating them in clays, zeolites, silica, alumina or other matrices to achieve high degree of stereoselectivity in the products, to reduce byproducts, to maximize rate of reaction. We illustrate the environmentally benign approach to 1,2-Oxazine-2- oxides, Michael addition, Wohl–Ziegler reaction, Acylation, Heck reaction, Tishchenko reaction, Diels– Alder reaction, Reformatsky and Luche Reaction, Oxidative coupling Reaction, Synthesis of chalcones, Synthesis of Dihydropyrimidinones

  4. Structure-property relationships for self-assembled zinc chlorin light-harvesting dye aggregates.

    Science.gov (United States)

    Huber, Valerie; Sengupta, Sanchita; Würthner, Frank

    2008-01-01

    A series of zinc 3(1)-hydroxymethyl chlorins 10 a-e and zinc 3(1)-hydroxyethyl chlorins 17 with varied structural features were synthesized by modifying naturally occurring chlorophyll a. Solvent-, temperature-, and concentration-dependent UV/Vis and CD spectroscopic methods as well as microscopic investigations were performed to explore the importance of particular functional groups and steric effects on the self-assembly behavior of these zinc chlorins. Semisynthetic zinc chlorins 10 a-e possess the three functional units relevant for self-assembly found in their natural bacteriochlorophyll (BChl) counterparts, namely, the 3(1)-OH group, a central metal ion, and the 13(1) C==O moiety along the Qy axis, and they contain various 17(2)-substituents. Depending on whether the zinc chlorins have 17(2)-hydrophobic or hydrophilic side chains, they self-assemble in nonpolar organic solvents or in aqueous media, respectively. Zinc chlorins possessing at least two long side chains provide soluble self-aggregates that are stable in solution for a prolonged time, thus facilitating elucidation of their properties by optical spectroscopy. The morphology of the zinc chlorin aggregates was elucidated by atomic force microscopy (AFM) studies, revealing well-defined nanoscale rod structures for zinc chlorin 10 b with a height of about 6 nm. It is worth noting that this size is in good accordance with a tubular arrangement of the dyes similar to that observed in their natural BChl counterparts in the light-harvesting chlorosomes of green bacteria. Furthermore, for the epimeric 3(1)-hydroxyethyl zinc chlorins 17 with hydrophobic side chains, the influence of the chirality center at the 3(1)-position on the aggregation behavior was studied in detail by UV/Vis and CD spectroscopy. Unlike zinc chlorins 10, the 3(1)-hydroxyethyl zinc chlorins 17 formed only small oligomers and not higher rod aggregate structures, which can be attributed to the steric effect imposed by the additional

  5. Thermodynamic dissociation constant studies of caffeine at different temperatures and in organic water solvent mixture.

    Science.gov (United States)

    Saeeduddin; Khanzada, A W K

    2004-01-01

    Thermodynamic dissociation studies have been carried out potentiometrically at various temperatures from 25 to 50 degrees C and in 10, 20, 30 and 40% v/v dioxane-water solvent mixture at 25 degrees C. The influence of temperature and nature of solvent on dissociation equilibria of caffeine is being investigated. A computer program in GW-BASIC has been used to calculate the pK values.

  6. Extraction of Betulin, Trimyristin, Eugenol and Carnosic Acid Using Water-Organic Solvent Mixtures

    OpenAIRE

    Lugemwa, Fulgentius N.

    2012-01-01

    A solvent system consisting of ethyl acetate, ethyl alcohol and water, in the volume ratio of 4.5:4.5:1, was developed and used to extract, at room temperature, betulin from white birch bark and antioxidants from spices (rosemary, thyme, sage, and oregano) and white oak chips. In addition, under reflux conditions, trimyristin was extracted from nutmeg using the same solvent system, and eugenol from olives was extracted using a mixture of salt water and ethyl acetate. The protocol demonstrates...

  7. Continuous hydrolysis of olive oil by immobilized lipase in organic solvent.

    Science.gov (United States)

    Yang, D; Rhee, J S

    1992-09-01

    Lipase (EC 3.1.1.3) from Candida rugosa was immobilized with DEAE-Sephadex A50, Sephadex G50, Sephadex LH-20, Amberlite IRA94, and Amberlite XAD-7. The enzyme immobilized with DEAE-Sephadex A50 was found to be most effective for continuous hydrolysis of olive oil in isooctane. For the continuous reaction, 0.2 g of dry immobilized enzyme was swollen with predetermined amount of water, and packed in a glass column reactor. When the organic solvent (Isooctane) containing olive oil substrate was co-currently fed with aqueous buffer, the two phases were evenly distributed throughout the packed bed without surfactant supplement or prior mixing of the two phases. A small amount of the surfactant (AOT) was used only in packing procedure, and no additional surfactant was necessary thereafter. Effects of initial water content of the swollen gel, buffer types, and strength were examined in the continuous reaction. Our results suggest that the operational half-life was affected by desorption of the bound enzyme. Under the conditions of 20% olive oil in isooctane and 25 mM triethanolamine buffer (pH 7.0), operational half life was 220 h at 30 degrees C. The reactor was also operable with n-hexane, but the operational stability of the immobilized enzyme in n-hexane was only half of that in isooctane. Our results indicate that various enzyme carrier having hydrophilic or amphiphilic properties could be used for two-phase continuous reaction in packed-bed column, reactor without any surfactant supply or prior dispersion of the two immiscible phases. PMID:18601176

  8. PAHs concentration and toxicity in organic solvent extracts of atmospheric particulate matter and sea sediments.

    Science.gov (United States)

    Ozaki, Noriatsu; Takeuchi, Shin-ya; Kojima, Keisuke; Kindaichi, Tomonori; Komatsu, Toshiko; Fukushima, Takehiko

    2012-01-01

    The concentration of polycyclic aromatic hydrocarbons (PAHs) and the toxicity to marine bacteria (Vibrio fischeri) were measured for the organic solvent extracts of sea sediments collected from an urban watershed area (Hiroshima Bay) of Japan and compared with the concentrations and toxicity of atmospheric particulate matter (PM). In atmospheric PM, the PAHs concentration was highest in fine particulate matter (FPM) collected during cold seasons. The concentrations of sea sediments were 0.01-0.001 times those of atmospheric PM. 1/EC50 was 1-10 L g(-1) PM for atmospheric PM and 0.1-1 L g(-1) dry solids for sea sediments. These results imply that toxic substances from atmospheric PM are diluted several tens or hundreds of times in sea sediments. The ratio of the 1/EC50 to PAHs concentration ((1/EC50)/16PAHs) was stable for all sea sediments (0.1-1 L μg(-1) 16PAHs) and was the same order of magnitude as that of FPM and coarse particulate matter (CPM). The ratio of sediments collected from the west was more similar to that of CPM while that from the east was more similar to FPM, possibly because of hydraulic differences among water bodies. The PAHs concentration pattern analyses (principal component analysis and isomer ratio analysis) were conducted and the results showed that the PAHs pattern in sea sediments was quite different to that of FPM and CPM. Comparison with previously conducted PAHs analyses suggested that biomass burning residues comprised a major portion of these other sources. PMID:22797225

  9. Organic solvents as risk factor for autoimmune diseases: a systematic review and meta-analysis.

    Directory of Open Access Journals (Sweden)

    Carolina Barragán-Martínez

    Full Text Available BACKGROUND: Genetic and epigenetic factors interacting with the environment over time are the main causes of complex diseases such as autoimmune diseases (ADs. Among the environmental factors are organic solvents (OSs, which are chemical compounds used routinely in commercial industries. Since controversy exists over whether ADs are caused by OSs, a systematic review and meta-analysis were performed to assess the association between OSs and ADs. METHODS AND FINDINGS: The systematic search was done in the PubMed, SCOPUS, SciELO and LILACS databases up to February 2012. Any type of study that used accepted classification criteria for ADs and had information about exposure to OSs was selected. Out of a total of 103 articles retrieved, 33 were finally included in the meta-analysis. The final odds ratios (ORs and 95% confidence intervals (CIs were obtained by the random effect model. A sensitivity analysis confirmed results were not sensitive to restrictions on the data included. Publication bias was trivial. Exposure to OSs was associated to systemic sclerosis, primary systemic vasculitis and multiple sclerosis individually and also to all the ADs evaluated and taken together as a single trait (OR: 1.54; 95% CI: 1.25-1.92; p-value<0.001. CONCLUSION: Exposure to OSs is a risk factor for developing ADs. As a corollary, individuals with non-modifiable risk factors (i.e., familial autoimmunity or carrying genetic factors should avoid any exposure to OSs in order to avoid increasing their risk of ADs.

  10. Reactions of Microsolvated Organic Compounds at Ambient Surfaces: Droplet Velocity, Charge State, and Solvent Effects

    Science.gov (United States)

    Badu-Tawiah, Abraham K.; Campbell, Dahlia I.; Cooks, R. Graham

    2012-06-01

    The exposure of charged microdroplets containing organic ions to solid-phase reagents at ambient surfaces results in heterogeneous ion/surface reactions. The electrosprayed droplets were driven pneumatically in ambient air and then electrically directed onto a surface coated with reagent. Using this reactive soft landing approach, acid-catalyzed Girard condensation was achieved at an ambient surface by directing droplets containing Girard T ions onto a dry keto-steroid. The charged droplet/surface reaction was much more efficient than the corresponding bulk solution-phase reaction performed on the same scale. The increase in product yield is ascribed to solvent evaporation, which causes moderate pH values in the starting droplet to reach extreme values and increases reagent concentrations. Comparisons are made with an experiment in which the droplets were pneumatically accelerated onto the ambient surface (reactive desorption electrospray ionization, DESI). The same reaction products were observed but differences in spatial distribution were seen associated with the "splash" of the high velocity DESI droplets. In a third type of experiment, the reactions of charged droplets with vapor phase reagents were examined by allowing electrosprayed droplets containing a reagent to intercept the headspace vapor of an analyte. Deposition onto a collector surface and mass analysis showed that samples in the vapor phase were captured by the electrospray droplets, and that instantaneous derivatization of the captured sample is possible in the open air. The systems examined under this condition included the derivatization of cortisone vapor with Girard T and that of 4-phenylpyridine N-oxide and 2-phenylacetophenone vapors with ethanolamine.

  11. Effect of Organic Solvent and Resin on Luminescent Capability of SrAl2O4:Eu2+, Dy3+ Phosphor

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Organic substance such as solvent and resin's effect on luminescent capability of SrAl2O4:Eu2+, Dy3+ phosphor was studied. Some organic solvents and resins were selected for experimentation. The results indicate that those organic solvents will not have negative effect on the applied capability of SrAl2O4:Eu2+, Dy3+ phosphor. Adopting the organic resins and covering method, the afterglow luminance of SrAl2O4:Eu2+, Dy3+ phosphor was increased by 85.01% and 82.51%.

  12. Inactivation of Chironomid Larvae with Chlorine Dioxide and Chlorine

    Institute of Scientific and Technical Information of China (English)

    SUN Xin-bin; CUI Fu-yi

    2008-01-01

    Chironomid larvae propagate prolifically in eutrophic water body and they cannot be exterminated by conventional disinfection process.The inactivation effects of chlorine and chlorine dioxide on Chironomid larvae were investigated and some boundary values in practice were determined under conditions of various oxidant dosage,organic precursor concentration and pH value.In addition,removal effect of differmt pre-oxidation combined with coagulation process on Chironomid larvae in law water was evaluated.It was found that chlorine dioxide possessed better inactivation effect than chlorine.Complete inactivation of Chironomid larvae in raw water was resulted by 1.5mg/L of chlorine dioxide with 30min of contact time. Additionally,the ocgallic precursor concentration,pH value had little influence on the inactivation effect.The coagulation jar test showed that Chironomid larvae in the raw water could be completely ronxwed by chlorine dioxide pre-oxidation in combination with the omgulation process at chlorine dioxide dosage of 0.8 mg/L.

  13. An Environmentally-Friendly and Catalytic Procedure for Mukaiyama Aldol Reaction Using Organic Catalyst DBU under Solvent Free Conditions

    Institute of Scientific and Technical Information of China (English)

    SHEN,Zhi-Liang; JI,Shun-Jun; LOH,Teck Peng

    2004-01-01

    @@ Recently, methods based exclusively on organic catalysts have become of major significance in synthetic chemistry.Mukaiyama-aldol reaction, as one of the most important and frequently utilized methods for C-C bond formation, is well documented in literatures recently. A variety of reagents, particularly metal-containing Lewis acids or bases, are known to promote the nucleophilic process. However, many of the reported strategies might have the following limitations from environmental viewpoints: (1) the use of metal-containing catalyst. Some of the catalysts are air or moisture sensitive (such as lithium amide), and crucial reaction conditions are needed; Some of the catalysts derived from poisonous metal (for example: SnCl4, SmI2 etc.) may cause harmful influence on humane body and environment; (2) the use of organic solvent (such as DMF, CH2Cl2 etc.) may bring about environmental pollution and solvent waste.

  14. Synergetic Solvent Engineering of Film Nanomorphology to Enhance Planar Perylene Diimide-Based Organic Photovoltaics.

    Science.gov (United States)

    Wang, Jialin; Liang, Ziqi

    2016-08-31

    Solvent additive has proven as a useful protocol for improving the film nanomorphology of polymer donor (D): fullerene acceptor (A) blends in bulk heterojunction (BHJ) photovoltaic cells. By contrast, the effect of such solvent additive on nonfullerene BHJ cells based on perylene diimide acceptor, for instance, is less effective because of their highly planar structure and strong π-aggregation in solid state. Here we choose N,N'-bis(1-ethylpropyl)-perylene-3,4,9,10-tetracarboxylic diimide (PDI) and thieno[3,4-b]thiophene-alt-benzodithiophene (PTB7) as a model D:A blend system to investigate how solvent engineering strategy synergistically impacts the blend film nanomorphology. Based on the differences of solvent volatility and solubility, various host solvents-chloroform (CF) and chlorobenzene (CB) and solvent additives-chloronaphthalene (CN) and 1,8-diiodooctane (DIO) are selected for comparative studies. It is found that the π-aggregation of PDIs can be largely suppressed by using low-boiling point (Tb) CF solvent, yet enlarged by using high-Tb CB. Moreover, CN additive provides good solubility of PDI molecules and hence reduces large PDI aggregates in CB system, while DIO exhibiting poor solubility works oppositely. By contrast, DIO that presents larger Tb difference with CF prolongs the film-forming, which assists in optimizing the PDI aggregation and increases the intermixed PTB7:PDI phases more significantly than CN in CF system, yielding the finest phase-separation morphology and balanced charge mobility. Consequently, the inverted BHJ cells based on CF-processed PTB7:PDI blend film with 0.4 vol % DIO exhibit the highest PCE of 3.55% with a fill factor of 56%, both of which are among the best performance for such a paradigm PTB7:PDI blend-based BHJ cells.

  15. Synergetic Solvent Engineering of Film Nanomorphology to Enhance Planar Perylene Diimide-Based Organic Photovoltaics.

    Science.gov (United States)

    Wang, Jialin; Liang, Ziqi

    2016-08-31

    Solvent additive has proven as a useful protocol for improving the film nanomorphology of polymer donor (D): fullerene acceptor (A) blends in bulk heterojunction (BHJ) photovoltaic cells. By contrast, the effect of such solvent additive on nonfullerene BHJ cells based on perylene diimide acceptor, for instance, is less effective because of their highly planar structure and strong π-aggregation in solid state. Here we choose N,N'-bis(1-ethylpropyl)-perylene-3,4,9,10-tetracarboxylic diimide (PDI) and thieno[3,4-b]thiophene-alt-benzodithiophene (PTB7) as a model D:A blend system to investigate how solvent engineering strategy synergistically impacts the blend film nanomorphology. Based on the differences of solvent volatility and solubility, various host solvents-chloroform (CF) and chlorobenzene (CB) and solvent additives-chloronaphthalene (CN) and 1,8-diiodooctane (DIO) are selected for comparative studies. It is found that the π-aggregation of PDIs can be largely suppressed by using low-boiling point (Tb) CF solvent, yet enlarged by using high-Tb CB. Moreover, CN additive provides good solubility of PDI molecules and hence reduces large PDI aggregates in CB system, while DIO exhibiting poor solubility works oppositely. By contrast, DIO that presents larger Tb difference with CF prolongs the film-forming, which assists in optimizing the PDI aggregation and increases the intermixed PTB7:PDI phases more significantly than CN in CF system, yielding the finest phase-separation morphology and balanced charge mobility. Consequently, the inverted BHJ cells based on CF-processed PTB7:PDI blend film with 0.4 vol % DIO exhibit the highest PCE of 3.55% with a fill factor of 56%, both of which are among the best performance for such a paradigm PTB7:PDI blend-based BHJ cells. PMID:27513281

  16. Malignant lymphoma and exposure to chemicals, especially organic solvents, chlorophenols and phenoxy acids: a case-control study.

    OpenAIRE

    Hardell, L; Eriksson, M.; Lenner, P; Lundgren, E.

    1981-01-01

    A number of men with malignant lymphoma of the histiocytic type and previous exposure to phenoxy acids or chlorophenols were observed and reported in 1979. A matched case-control study has therefore been performed with cases of malignant lymphoma (Hodgkin's disease and non-Hodgkin lymphoma). This study included 169 cases and 338 controls. The results indicate that exposure to phenoxy acids, chlorophenols, and organic solvents may be a causative factor in malignant lymphoma. Combined exposure ...

  17. Synthesis of Monolithic Fe2O3-Al2O3 Composite Aerogels via Organic Solvent Sublimation Drying

    Directory of Open Access Journals (Sweden)

    Lili Ren

    2016-01-01

    Full Text Available Monolithic Fe2O3-Al2O3 composite aerogels have been prepared successfully via organic solvent sublimation drying method. The results show that a new phase forms when the right amount of ferric oxide is added to the alumina aerogel. From the TEM pictures we can see a shuttle-type structure with the length of about 15 nm forms, which leads to the high surface areas of composited aerogel.

  18. Selection and evaluation of alternative solvents for caprolactam extraction

    NARCIS (Netherlands)

    Delden, van Mathijs L.; Kuipers, Norbert J.M.; Haan, de André B.

    2006-01-01

    Because of the strict legislation for currently applied solvents in the industrial extraction of caprolactam, being benzene, toluene and chlorinated hydrocarbons, a need exists for alternative, environmentally benign solvents. An experimental screening procedure consisting of several steps was used

  19. ``Living polymers'' in organic solvents : stress relaxation in bicopper tetracarboxylate/tert-butyl cyclohexane solutions

    Science.gov (United States)

    Terech, P.; Maldivi, P.; Dammer, C.

    1994-10-01

    Viscoelastic solutions of a bicopper tetracarboxylate complex in tert-butylcyclohexane have been studied by dynamic rheology in a wide range of concentrations (0.5-1.5 % volume fraction). The zero shear viscosity, the elastic modulus, the terminal stress relaxation time and the height of the high-frequency dip, in a Cole-Cole representation of the complex elastic modulus, follow scaling laws. The related exponents are discussed in the context of the physics of “living polymers” : a term used to describe worm-like species undergoing scission/recombination reactions competing mainly with the reptation motions of the chains. The current system, made up of molecular threads (17.5 Å diameter) of Cu2(O2C-CH(C2H5)C4H9)4 in the apolar solvent, is representative of a “living polymer” where, instead of mechanisms involving transient star polymeric crosslinks, a reversible scission mechanism prevails. The dynamics in the high-frequency range evolves from a regime where reptation is the dominant relaxation mechanism to a cross-over regime where “breathing” fluctuations and Rouse motions become important. Large modifications of the stress relaxation function occur for more concentrated systems. The binary system is the first example of a “living polymer” in an organic solvent and exhibits elastic moduli (G ≈ ca. 120 Pa à φ = 1 %) which are at least 20 times larger than those found for the aqueous “living polymer” systems. Les solutions viscoélastiques d'un tétracarboxylate binucléaire de cuivre dans le tert-butylcyclohexane sont étudiées par rhéologie en mode dynamique dans une gamme étendue de concentrations (0,5 %-15,5 %). La viscosité à gradient nul, le module élastique, le temps terminal de relaxation et la hauteur du puits à haute fréquence, dans une représentation Cole-Cole du module élastique complexe, suivent des lois d'échelles. Les exposants correspondants sont discutés dans le contexte de la physique des “polymères vivants

  20. Liver function tests and urinary albumin in house painters with previous heavy exposure to organic solvents.

    Science.gov (United States)

    Lundberg, I; Nise, G; Hedenborg, G; Högberg, M; Vesterberg, O

    1994-05-01

    The serum activities or concentrations of aspartate aminotransferase (ASAT), alanine aminotransferase (ALAT), alkaline phosphatase (ALP), albumin, gamma-glutamyl transpeptidase (GGT), bilirubin (BIL), cholic acid (CHOL), chenodeoxycholic acid (CHENO), and transferrin with isoelectric point 5.7, and the urinary excretion of albumin were determined among male current or former house painters (n = 135) and house carpenters (n = 71) who had worked in their trades for at least 10 years before 1970. Workers who showed a value above the 90th percentile among the carpenters in at least one of the tests ASAT, ALAT, GGT, BIL, CHOL, or CHENO were regarded as showing "possible signs of liver dysfunction". Each participant's lifetime solvent exposure was evaluated by interview. The painters were divided into categories with low, intermediate, and heavy cumulative exposure during life (LTSE) or during the most exposed year (MEYSE). All participants stated none or slight recent exposure. The prevalence of possible signs of liver dysfunction increased with solvent exposure category according to LTSE as well as MEYSE with a numerically higher risk estimate in the heavy exposure category for MEYSE than for LTSE. ALP activity increased with exposure category according to both exposure estimates. This increase seemed to be due to an interaction between exposure to solvents and current or previous long term intake of medicines potentially toxic to the liver. None of these results was affected by whether or not the subjects had been exposed to solvents during the year before the investigation. The exposure to solvents was not significantly related to any other outcome variable. It is concluded that long term heavy exposure to solvents may elicit changes in conventional liver function tests indicative of a mild chronic effect on the liver. The findings also suggest that heavy solvent exposure during short time periods is a more likely cause of the findings than lifetime cumulative

  1. Direct and ultrasensitive optofluidic-based immunosensing assay of aflatoxin M1 in dairy products using organic solvent extraction.

    Science.gov (United States)

    Lou, Xuening; Zhu, Anna; Wang, Hongliang; Wu, Jun; Zhou, Liping; Long, Feng

    2016-10-12

    Aflatoxin M1 (AFM1), a highly toxic secondary metabolite, is present in a wide range of dairy products. In this study, we designed a simple, low-cost, reusable, and easy-to-operate immunosensing method for ultrasensitive detection of AFM1 in dairy products by using a portable evanescent wave-based optofluidic biosensing platform (EOBP). The developed method provides the minimum detection limit of 5 ng/L, which is below the most restrictive standard imposed by the current regulations for AFM1 in dairy products. The effect of several organic solvents, such as methanol, acetone, and acetonitrile, on the binding reaction of antibody-antigen in heterogeneous and homogeneous solutions was evaluated. Although the effect of organic solvents on the homogeneous binding reaction between antibody and antigen is more significant than that of heterogeneous binding reaction between antibody in solution and antigen immobilized onto the sensor surface, the fluorescence signal detected by EOBP is linearly dependent on AFM1 concentration. Therefore, AFM1 can be directly quantified even if the samples contain a certain organic solvent concentration. The robustness and stability of AFM1-ovalbumin conjugate allow the regeneration of modified biosensor surface for more than 200 times, thereby achieving a cost-effective and reliable AFM1 determination. The proposed method provides a rapid, ultrasensitive, and reliable AFM1 determination in dairy products without complicated sample pretreatment process. PMID:27662766

  2. Expressions for multilinear combined pH/organic solvent elution of ionizable analytes in reversed-phase HPLC.

    Science.gov (United States)

    Zisi, Ch; Fasoula, S; Pappa-Louisi, A; Nikitas, P

    2013-10-15

    Expressions for the retention time of ionogenic analytes eluted under multilinear double pH/solvent-gradients in reversed-phase liquid chromatography are developed by dividing each gradient profile into a finite number of subportions, where the solute retention factors or their logarithms vary linearly with time. To test the theory, two series of experimental gradient retention data of amino acid OPA derivatives were analyzed: The first one was a monolinear or bilinear pH-gradient data set obtained in eluents with different but constant organic modifier contents, whereas the second data set comprised retention data of combined pH/organic solvent-gradients, where the organic content was changed linearly with time but the variation of pH exhibited a curved form approximated by five linear subportions. It was found that the derived expressions describe these experimental retention data with high accuracy, since under double pH/solvent-gradients the overall errors in the fitted and predicted retention times were 1.9% and 1.7%, respectively, whereas under simple pH-gradients these errors were 0.9% and 2%, respectively. PMID:24010983

  3. Effect of organic co-solvents on the solvation enthalpies of amino acids and dipeptides in mixed aqueous solutions

    Science.gov (United States)

    Badelin, V. G.; Tyunina, E. Yu.

    2011-09-01

    Transition enthalpies (Δtr H o) of substances from water to binary solutions were calculated at 298.15 K on the basis of standard dissolution enthalpies (Δsol H o) for six amino acids and five dipeptides in the mixtures of water with organic solvents of various chemical natures. The enthalpy pair coefficients of interaction h xy for biomolecules with organic component of mixture were estimated within the formalism of the McMillan-Mayer theory. The change in the character of the interaction of the components of solution was demonstrated in dependence on the physicochemical properties of the solvent and nature of the side radical of the dissolved bioorganic substance. Quantitative estimation of the type of interaction of the substance with the solvent was performed on the basis of correlation ratios relating the enthalpy characteristics of bioorganic substances to properties of organic cosolvents. It was shown that in the solutions under study, the effects of both the specific (mainly electron donor) and non-specific solvation of amino acids and peptides are observed.

  4. Renal and hepatotoxic alterations in adult mice on inhalation of specific mixture of organic solvents.

    Science.gov (United States)

    Ketan, Vaghasia K; Bhavyata, Kalariya; Linzbuoy, George; Hyacinth, Highland N

    2015-12-01

    This study was aimed at investigating alterations in renal and hepatic toxicity induced by exposing to a combination of three solvents, namely, benzene, toluene and xylene in adult mice. The mice were divided into three groups (control, low-dose-treated (450 ppm) and high-dose (675 ppm) groups) using randomization methods. The treated groups were exposed to vapours of a mixture of benzene, toluene and xylene at doses of 450 and 675 ppm, for 6 h day(-1) for a short-term of 7-day exposure period. The study revealed that the solvent exposure resulted in an increase in the weight of liver and kidney as compared to the control. Biochemical analyses indicated a significant decline in the activities of superoxide dismutase and catalase in both the treated groups, with concomitant increase in lipid peroxidation. Liver aminotransferases (alanine aminotransferase and aspartate aminotransferase) were elevated with significant alterations in the levels of protein, creatinine and cholesterol in these tissues upon solvent exposure. Correlated with these changes, serum thyroid hormones T3 and T4 were also significantly altered. This study, therefore, demonstrates that inhalation of vapours from the solvent mixture resulted in significant dose-dependent biochemical and functional changes in the vital tissues (liver and kidney) studied. The study has specific relevance since humans are increasingly being exposed to such solvents due to increased industrial use in such combinations.

  5. Solvent resistant nanofiltration membranes

    OpenAIRE

    Dutczak, Szymon Maria

    2011-01-01

    This thesis describes preparation and characterization of membranes for organic solvent filtration (OSF). The main aim was developing membranes for solvent resistant nanofiltration (SRNF) with molecular weight cut-off below 500 g mol-1.

  6. The aerobic oxidation of alcohols with a ruthenium porphyrin catalyst in organic and fluorinated solvents.

    Science.gov (United States)

    Korotchenko, Vasily N; Severin, Kay; Gagné, Michel R

    2008-06-01

    Carbonylruthenium tetrakis(pentafluorophenyl)porphyrin Ru(TPFPP)(CO) was utilized for the aerobic oxidation of alcohols. The in situ activation of the catalyst with mCPBA provided a species capable of catalyzing the oxidation of alcohols with molecular oxygen. The choice of solvent and additive was crucial to obtaining high activity and selectivity. Secondary aromatic alcohols were oxidized in the presence of the ruthenium porphyrin and tetrabutyl ammonium hydroxide in the solvent bromotrichloromethane, enabling high yields to be achieved (up to 99%). Alternatively, alcohols could be oxidized in perfluoro(methyldecalin) with the ruthenium porphyrin at higher temperatures (140 degrees C) and elevated oxygen pressures (50 psi).

  7. The solvent-extractable organic compounds in the Indonesia biomass burning aerosols - characterization studies

    Science.gov (United States)

    Fang, M.; Zheng, M.; Wang, F.; To, K. L.; Jaafar, A. B.; Tong, S. L.

    The large-scale air pollution episode due to the out-of-control biomass burning for agricultural purposes in Indonesia started in June 1997, has become a severe environmental problem for itself and the neighboring countries. The fire lasted for almost five months. Its impact on the health and ecology in the affected areas is expected to be substantial, costly and possibly long lasting. Air pollution Index as high as 839 has been reported in Malaysia. API is calculated based on the five pollutants: NO 2, SO 2, O 3, CO, and respirable suspended particulates (PM10). It ranges in value from 0 to 500. An index above 101 is considered to be unhealthy and a value over 201 is very unhealthy (Abidin and Shin, 1996). The solvent-extractable organic compounds from four total suspended particulate (TSP) high-volume samples collected in Kuala Lumpur, Malaysia (Stations Pudu and SIRIM) were subjected to characterization - the abundance was determined and biomarkers were identified. Two of the samples were from early September when the fire was less intense, while the other two were from late September when Kuala Lumpur experienced very heavy smoke coverage which could be easily observed from NOAA/AVHRR satellite images. The samples contained mainly aliphatic hydrocarbons such as n-alkanes and triterpanes, alkanoic acids, alkanols, and polycyclic aromatic hydrocarbons. The difference between the early and late September samples was very significant. The total yield increased from 0.6 to 24.3 μg m -3 at Pudu and 1.9 to 20.1 μg m -3 at SIRIM, with increases in concentration in every class. The higher input of vascular plant wax components in the late September samples, when the fire was more intense, was characterized by the distribution patterns of the homologous series n-alkanes, n-alkanoic acids, and n-alkanols, e.g., lower U : R, higher >C 22/C 20/haze episode on 29 September 1991 in Kuala Lumpur, Malaysia (Abas and Simoneit, 1996).

  8. Organic solvent-free cloud point extraction-like methodology using aggregation of graphene oxide.

    Science.gov (United States)

    Deng, Dongyan; Jiang, Xiaoming; Yang, Lu; Hou, Xiandeng; Zheng, Chengbin

    2014-01-01

    Because of its unique properties and capability of formation of well-dispersed aqueous colloids in aqueous phase, graphene oxide can be used for the efficient preconcentration of heavy metal ions prior to their determination. The complete collection of graphene oxide colloids from water has generally been considered to be insurmountable. Here, graphene oxide aggregation triggered by introducing NaCl was used to develop a novel organic solvent-free cloud point extraction-like method for the determination of trace toxic metals. The graphene oxide sheets were uniformly dispersed in aqueous samples or standard solutions for a fast and efficient adsorption of Pb(II), Cd(II), Bi(III), and Sb(III) owing to its hydrophilic character and the electrostatic repulsion among the graphene oxide sheets, and its aggregation immediately occurred when the electrostatic repulsion was eliminated via adding NaCl to neutralize the excessive negative charges on the surface of graphene oxide sheets. The aggregates of graphene oxide and analytes ions were separated and treated with hydrochloric acid to form a slurry solution. The slurry solution was pumped to mix with KBH4 solution to generate hydrides, which were subsequently separated from the liquid phase and directed to an atomic fluorescence spectrometer or directly introduced to an inductively coupled plasma optical emission spectrometer for detection. On the basis of a 50 mL sample volume, the limits of detection of 0.01, 0.002, 0.01, and 0.006 ng mL(-1) were obtained for Pb, Cd, Bi, and Sb, respectively, when using atomic fluorescence spectrometry, providing 35-, 8-, 36-, and 37-fold improvements over the conventional method. Detection limits of 0.6, 0.15, 0.1, and 1.0 ng mL(-1) were obtained with the use of slurry sampling inductively coupled plasma optical emission spectrometry. The method was applied for analysis of two Certified Reference Materials and three water samples for these elements.

  9. Voltammetric Studies on Vitamins D2 and D3 in Organic Solvents

    International Nuclear Information System (INIS)

    Highlights: • Vitamins D2 and D3 undergo a chemically irreversible oxidation process. • The electrochemical oxidation occurs via one-electron on short (CV) time-scales. • On long time scales (electrolysis) the oxidation occurs via two-electrons. • Chemical oxidation was performed using two molar equivalents of NO+. • Oxidation occurs at the triene moiety. - Abstract: The electrochemical behavior of vitamins D2 and D3 were examined by performing cyclic voltammetry (CV), rotating disk electrode voltammetry, controlled potential electrolysis and chemical oxidation in aprotic organic solvents. Both vitamins were electrochemically oxidized in dichloromethane and acetonitrile (Epox ∼ +0.8 vs. (Fc/Fc+)/V, where Epox is the anodic peak potential and Fc = ferrocene) via a one-electron chemically irreversible process on the short voltammetric time scale (≤ seconds). Varying the scan rate (0.1 V s−1 to 20 V s−1) and temperature (233 K to 293 K) did not strongly affect the voltammetric response recorded on platinum and glassy carbon electrode surfaces with the oxidation process remaining chemically irreversible over the range of scan rates and temperatures tested, indicating that the initially formed cation radical was not long-lived. Repetitive CV experiments indicated that the oxidized product partially adsorbed onto the electrode surface, resulting in diminishing peak currents with multiple scans. Bulk controlled potential electrolysis of the vitamin D compounds performed by alternating several cycles of oxidative electrolysis and reductive pulsed stripping proved to be effective in stripping the adsorbed species off the electrode surfaces. Longer time scale bulk electrolysis experiments led to the detection of a new oxidation peak appearing at less positive potentials as the electrolysis progressed, suggesting that the compounds underwent oxidation on long time scales (minutes to hours) via a two electron process. The vitamins were most likely initially

  10. System Development from Organic Solvents to Ionic Liquids for Synthesiz-ing Ascorbyl Esters with Conjugated Linoleic Acids

    DEFF Research Database (Denmark)

    Yang, Zhiyong; Schultz, Lise; Guo, Zheng;

    2012-01-01

    -ferred to an ionic liquid system for the purpose of improving solubility of the polar substrate and avoiding the application of organic solvents. From screening experiments, it was evident that only methyltrioctylammonium triflouroacetate (tO-MA·TFA) could provide a proper reaction environment for production...... of ascorbyl-CLA ester when using Novozym® 435 as biocatalyst. It was possible to significantly increase the productivity (150 g/l) through the increase of ascorbic acid sol-ubility in ionic liquids by super saturation together with the increase of reaction temperature to 70°C, far beyond than that in organic...

  11. Influence of organic solvents on catalytic behaviors and cell morphology of whole-cell biocatalysts for synthesis of 5'-arabinocytosine laurate.

    Directory of Open Access Journals (Sweden)

    Meiyan Yang

    Full Text Available A whole-cell based method was developed for the regioselective synthesis of arabinocytosine laurate. Among the seven kinds of bacteria strains tested in the acylation reaction, Pseudomonas fluorescens gave the highest productivity and a higher 5'-regioselectivity than 99%. Compared with pure organic solvents, the use of organic solvent mixtures greatly promoted the yield of the whole-cell catalyzed reaction, but showed little influence on the 5'-regioselectivity. Of all the tested solvent mixtures, the best reaction result was found in isopropyl ether/pyridine followed by isopentanol/pyridine. However, the whole-cells showed much lower thermostability in isopropyl ether/pyridine than in THF-pyridine. To better understand the toxic effects of the organic solvents on P. fluorescens whole-cells and growing cells were further examined. Significant influences of organic solvents on the biomass of the cells were found, which differed depending on the type of solvents used. SEM analysis visually revealed the changes in the surface morphology of whole-cells and growing cells cultured in media containing various organic solvents, in terms of surface smoothness, bulges and changed cell sizes. Results demonstrated that organic toxicity to cell structure played an important role in whole-cell mediated catalysis.

  12. Influence of organic solvents on catalytic behaviors and cell morphology of whole-cell biocatalysts for synthesis of 5'-arabinocytosine laurate.

    Science.gov (United States)

    Yang, Meiyan; Wu, Hui; Lian, Yan; Li, Xiaofeng; Lai, Furao; Zhao, Guanglei

    2014-01-01

    A whole-cell based method was developed for the regioselective synthesis of arabinocytosine laurate. Among the seven kinds of bacteria strains tested in the acylation reaction, Pseudomonas fluorescens gave the highest productivity and a higher 5'-regioselectivity than 99%. Compared with pure organic solvents, the use of organic solvent mixtures greatly promoted the yield of the whole-cell catalyzed reaction, but showed little influence on the 5'-regioselectivity. Of all the tested solvent mixtures, the best reaction result was found in isopropyl ether/pyridine followed by isopentanol/pyridine. However, the whole-cells showed much lower thermostability in isopropyl ether/pyridine than in THF-pyridine. To better understand the toxic effects of the organic solvents on P. fluorescens whole-cells and growing cells were further examined. Significant influences of organic solvents on the biomass of the cells were found, which differed depending on the type of solvents used. SEM analysis visually revealed the changes in the surface morphology of whole-cells and growing cells cultured in media containing various organic solvents, in terms of surface smoothness, bulges and changed cell sizes. Results demonstrated that organic toxicity to cell structure played an important role in whole-cell mediated catalysis.

  13. Human monitoring of exposure to organic solvents. I Benzene, phenol, toluene, cresols and xylenes

    NARCIS (Netherlands)

    Jansen EHJM; de Fluiter P; TOX

    1994-01-01

    In this report the conclusions of a literature study has been summarized concerning the monitoring of the general population to exposure to benzene-like solvents. Since the Dutch population is exposed to concentrations far below the ppm level, the conclusions on the suitability of biomarkers are ba

  14. The effect of aqueous organic solvents on the dissociation constants and thermodynamic properties of alkanolamines

    NARCIS (Netherlands)

    Hamborg, Espen S.; van Aken, Coen; Versteeg, Geert F.

    2010-01-01

    The dissociation constants of protonated monoethanolamine and N-methyldiethanolamine have been determined in methanol-water, ethanol-water, and t-butanol-water solvents. The alcohol mole fractions were ranging from 0.2 to 0.95 and the temperatures from 283 to 323 K, 283 to 333 K, and at 298.15 K, re

  15. Medium-based optimization of an organic solvent-tolerant extracellular lipase from the isolated halophilic Alkalibacillus salilacus.

    Science.gov (United States)

    Samaei-Nouroozi, Amene; Rezaei, Shahla; Khoshnevis, Nika; Doosti, Mahmoud; Hajihoseini, Reza; Khoshayand, Mohammad Reza; Faramarzi, Mohammad Ali

    2015-09-01

    A haloalkaliphilic solvent-tolerant lipase was produced from Alkalibacillus salilacus within 48 h of growth in liquid medium. An overall 4.9-fold enhanced production was achieved over unoptimized media after medium optimization by statistical approaches. Plackett-Burman screening suggested lipase production maximally influenced by olive oil, KH2PO4, NaCl, and glucose; and response surface methodology predicted the appropriate levels of each parameter. Produced lipase was highly active and stable over broad ranges of temperature (15-65 °C), pH (4.0-11.0), and NaCl concentration (0-30 %) showing excellent thermostable, pH-stable, and halophilic properties. The enzyme was optimally active at pH 8.0 and 40 °C. Majority of cations, except some like Co(2+) and Al(3+) were positive signals for lipase activity. In addition, the presence of chemical agents and organic solvents with different log P ow was well tolerated by the enzyme. Finally, efficacy of lipase-mediated esterification of various alcohols with oleic acid in organic solvents was studied. PMID:26198037

  16. Advanced solvent based methods for molecular characterization of soil organic matter by high-resolution mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Tfaily, Malak M.; Chu, Rosalie K.; Tolic, Nikola; Roscioli, Kristyn M.; Anderton, Christopher R.; Pasa-Tolic, Ljiljana; Robinson, Errol W.; Hess, Nancy J.

    2015-05-19

    Soil organic matter (SOM) a complex, heterogeneous mixture of above and belowground plant litter and animal and microbial residues at various degrees of decomposition, is a key reservoir for carbon (C) and nutrient biogeochemical cycling in soil based ecosystems. A limited understanding of the molecular composition of SOM limits the ability to routinely decipher chemical processes within soil and predict accurately how terrestrial carbon fluxes will response to changing climatic conditions and land use. To elucidate the molecular-level structure of SOM, we selectively extracted a broad range of intact SOM compounds by a combination of different organic solvents from soils with a wide range of C content. Our use of Electrospray ionization (ESI) coupled with Fourier transform ion cyclotron resonance mass spectrometry (FTICR MS) and a suite of solvents with varying polarity significantly expands the inventory of the types of organic molecules present in soils. Specifically, we found that hexane is selective for lipid-like compounds with very low O:C ratios; water was selective for carbohydrates with high O:C ratios; acetonitrile preferentially extracts lignin, condensed structures, and tannin poly phenolic compounds with O:C > 0.5; methanol has higher selectivity towards compounds characterized with low O:C < 0.5; and hexane, MeOH, ACN and water solvents increase the number and types of organic molecules extracted from soil for a broader range of chemically diverse soil types. Our study of SOM molecules by ESI-FTICR MS revealed new insight into the molecular-level complexity of organics contained in soils.

  17. Application of gas chromatography analysis to quality control of residual organic solvents in clopidogrel bisulphate

    Directory of Open Access Journals (Sweden)

    Pavlović Aleksandar D.

    2014-01-01

    Full Text Available A direct-injection, split-mode capillary gas chromatographic procedure with a flame ionization detection is developed for the analysis of eight solvents used in the synthesis and purification of an anti-thrombotic drug clopidogrel bisulphate. The solvents analyzed were methanol, acetone, dichloromethane (DCM, 2-butanol, cyclohexane, toluene, acetic acid and N, N-dimethyl formamide (DMF. In addition, as a result of dehydration of 2-butanol during drying process, in clopidogrel bisulphate samples, significant amounts of 2-butanol dehydration products (1-butene, cis and trans isomers of 2-butene, 2,2'-oxydibutane and 1-(1-methylpropoxybutane may be detected. The content of each of these volatile products can be evaluated using the same gas-chromatographic method, with quantification based on the response factor established for the chromatographic peak of 2-butanol. For each solvent used in the process of clopidogrel bisulphate preparation, the procedure is validated for selectivity, linearity, recovery, precision, robustness, quantitation limit, and detection limit. All eight solvents plus five 2-butanol degradation products are fully separated. System suitability test is validated, and requirements are set. Based on a large number of result sets, retrospectively, from many different batches analyzed, conclusions were made about process variations and reliability and a lack of consistency was identified in the quality of the active substance from a particular producer source. Multivariate analysis was used as statistical technique to classify samples. From the analyzed set of 11 solvents, 6 of them were preselected based upon their occurrence in the samples and both Principal Component Analysis (PCA and Hierarchical Cluster Analysis (HCA were performed.

  18. Large-area bi-component processing of organic semiconductors by spray deposition and spin coating with orthogonal solvents

    Energy Technology Data Exchange (ETDEWEB)

    Treossi, Emanuele; Liscio, Andrea; Palermo, Vincenzo [Consiglio Nazionale delle Ricerche, Istituto per la Sintesi Organica e la Fotoreattivita, Bologna (Italy); Feng, Xinliang; Muellen, Klaus [Max-Planck Institute for Polymer Research, Mainz (Germany); Samori, Paolo [Universite Louis Pasteur, Nanochemistry Laboratory, ISIS-CNRS, Strasbourg (France); Consiglio Nazionale delle Ricerche, Istituto per la Sintesi Organica e la Fotoreattivita, Bologna (Italy)

    2009-04-15

    Micrometre-thick uniform layers of a polymeric semiconductor (poly(3-hexylthiophene), P3HT) have been fabricated from solution by spray deposition making use of a commercial airbrush. Multi-scale characterization by optical microscopy and atomic force microscopy revealed the formation of smooth layers featuring reproducible patterns of spatially correlated micron-sized holes. This morphology was found to be uniform over the whole sample surface, on millimetre scale. On this micro-patterned P3HT layer an orthogonal solvent (i.e. a solvent which does not dissolve the P3HT) has been employed to deposit either by spin coating or by drop casting a second organic semiconductor. While spin-coated films exhibited nano-crystals of an alkylated perylene tetracarboxy diimide (PDI) preferentially grown into the micro-fabricated holes, drop-cast films displayed crystalline PDI fibres adsorbed on the patterned surface in random positions. (orig.)

  19. Large-area bi-component processing of organic semiconductors by spray deposition and spin coating with orthogonal solvents

    Science.gov (United States)

    Treossi, Emanuele; Liscio, Andrea; Feng, Xinliang; Palermo, Vincenzo; Müllen, Klaus; Samorì, Paolo

    2009-04-01

    Micrometre-thick uniform layers of a polymeric semiconductor (poly(3-hexylthiophene), P3HT) have been fabricated from solution by spray deposition making use of a commercial airbrush. Multi-scale characterization by optical microscopy and atomic force microscopy revealed the formation of smooth layers featuring reproducible patterns of spatially correlated micron-sized holes. This morphology was found to be uniform over the whole sample surface, on millimetre scale. On this micro-patterned P3HT layer an orthogonal solvent (i.e. a solvent which does not dissolve the P3HT) has been employed to deposit either by spin coating or by drop casting a second organic semiconductor. While spin-coated films exhibited nano-crystals of an alkylated perylene tetracarboxy diimide (PDI) preferentially grown into the micro-fabricated holes, drop-cast films displayed crystalline PDI fibres adsorbed on the patterned surface in random positions.

  20. Application of method of organizational congruences to substitution of organic solvents with vegetable agents for cleaning offset printing machine

    Energy Technology Data Exchange (ETDEWEB)

    Salerno, S. [ENEA, Casaccia (Italy). Area Energia Ambiente e Salute; Tartaglia, R. [Unita Sanitaria Locale 10/D, Firenze (Italy); Garzi, S.; Biagioni, A. [Istituto tecnico Leonardo da Vinci, Firenze (Italy)

    1995-06-01

    The aim of this research is the application of the method of organizational congruences before and after the substitution of organic solvents with vegetable agents for the cleaning offset printing machine in order to assess the organizational changes. A solvent free process is the goal of the SUBSPRINT project (Technology Transfer Program of the European Community). In this study it is shown how human and environmental health is improved by using vegetable agents through this change may lead to some other organizational constraints such as the time needed, the monotony and repetitiveness of the technical actions involved. The authors underline that the knowledge of the new technology impact of health help for a better understanding of the resistance to the change and help for a further amelioration of it.

  1. Formation of bromate and halogenated disinfection byproducts during chlorination of bromide-containing waters in the presence of dissolved organic matter and CuO

    KAUST Repository

    Liu, Chao

    2015-12-02

    Previous studies showed that significant bromate (BrO3-) can be formed via the CuO-catalyzed disproportionation of hypobromous acid (HOBr) pathway. In this study, the influence of CuO on the formation of BrO3- and halogenated disinfection byproducts (DBPs) (e.g., trihalomethanes, THMs and haloacetic acids, HAAs) during chlorination of six dissolved organic matter (DOM) isolates was investigated. Only in the presence of slow reacting DOM (from treated Colorado River water, i.e., CRW-BF-HPO), significant BrO3- formation is observed, which competes with bromination of DOM (i.e., THM and HAA formation). Reactions between HOBr and 12 model compounds in the presence of CuO indicates that CuO-catalyzed HOBr disproportionation is completely inhibited by fast reacting phenols, while it predominates in the presence of practically unreactive compounds (acetone, butanol, propionic, and butyric acids). In the presence of slow reacting di- and tri-carboxylic acids (oxalic, malonic, succinic, and citric acids), BrO3- formation varies, depending on its competition with bromoform and dibromoacetic acid formation (i.e., bromination pathway). The latter pathway can be enhanced by CuO due to the activation of HOBr. Therefore, increasing CuO dose (0-0.2 g L-1) in a reaction system containing chlorine, bromide, and CRW-BF-HPO enhances the formation of BrO3-, total THMs and HAAs. Factors including pH and initial reactant concentrations influence the DBP formation. These novel findings have implications for elevated DBP formation during transportation of chlorinated waters in copper-containing distribution systems.

  2. Influência de solventes orgânicos na adsorção de linalol e decanal em sílica gel Influence of organic solvents on adsorption of linalool and decanal on silica gel

    Directory of Open Access Journals (Sweden)

    Adriana Régia Cornélio

    2004-08-01

    Full Text Available Estudou-se a influência de solventes orgânicos (etanol, propanol e acetato de etila na isoterma de adsorção de uma solução-modelo do óleo essencial de laranja em sílica-gel. A solução-modelo constituiu-se de compostos oxigenados (linalol e decanal dissolvidos em d-limoneno (solvente. A influência da temperatura no processo de adsorção foi determinada para sistemas ternário (d-limoneno + linalol + decanal à temperatura de 298,15 K. Para o composto oxigenado decanal, os solventes que mais influenciaram no processo de adsorção foram o etanol e o acetato de etila; já para o linalol, todos os solventes estudados tiveram influência sobre o processo.The influence of organic solvents (ethanol, propanol and ethyl acetate on the isotherm of adsorption of model solutions of orange essential oil on silica gel was investigated. The model solution consisted of oxygenated compounds (linalool and decanal dissolved in d-limoneno. The influence of temperature on the process of adsorption was determined by ternary systems (d-limoneno + linalool + decanal at the temperature of 298,15 K . For the oxygenated compound decanal, the solvents that showed greater influence on the process of adsorption were ethanol and ethyl acetate, and for linalool all of the solvents studied were shown to influence the process.

  3. Solvent substitutes

    International Nuclear Information System (INIS)

    The environmental and industrial hygiene regulations promulgated since 1980, most notably the Superfund Amendments and Reauthorization Act (SARA), the Hazardous and Solid Waste Amendments to the Resources Conservation and Recovery Act (RCRA), and the Clean Air Act Amendments of 1990, have brought about an increased emphasis on user exposure, hazardous waste generation, and air emissions. As a result, industry is performing a fundamental reassessment of cleaning solvents, processes, and procedures. The more progressive organizations have made their goal the elimination of solvents that may pose significant potential human health and environmental hazards. This chapter discusses solvent cleaning in metal-finishing, metal-manufacturing, and industrial maintenance applications; precision cleaning; and electronics manufacturing. Nonmetallic cleaning, adhesives, coatings, inks, and aerosols also will be addressed, but in a more cursory manner

  4. Organic solvent and temperature-enhanced ion chromatography-high resolution mass spectrometry for the determination of low molecular weight organic and inorganic anions

    International Nuclear Information System (INIS)

    Highlights: • IC selectivity at high contents of organic solvent in eluent and elevated temperature is studied. • Solvent-enhanced IC coupled to high resolution MS is beneficial for sensitive detection of ions. • The first application of IC-HRMS to the detection of low explosives in fingermarks is shown. - Abstract: There has recently been increased interest in coupling ion chromatography (IC) to high resolution mass spectrometry (HRMS) to enable highly sensitive and selective analysis. Herein, the first comprehensive study focusing on the direct coupling of suppressed IC to HRMS without the need for post-suppressor organic solvent modification is presented. Chromatographic selectivity and added HRMS sensitivity offered by organic solvent-modified IC eluents on a modern hyper-crosslinked polymeric anion-exchange resin (IonPac AS18) are shown using isocratic eluents containing 5–50 mM hydroxide with 0–80% methanol or acetonitrile for a range of low molecular weight anions (<165 Da). Comprehensive experiments on IC thermodynamics over a temperature range between 20–45 °C with the eluent containing up to 60% of acetonitrile or methanol revealed markedly different retention behaviour and selectivity for the selected analytes on the same polymer based ion-exchange resin. Optimised sensitivity with HRMS was achieved with as low as 30–40% organic eluent content. Analytical performance characteristics are presented and compared with other IC-MS based works. This study also presents the first application of IC-HRMS to forensic detection of trace low-order anionic explosive residues in latent human fingermarks

  5. Organic solvent and temperature-enhanced ion chromatography-high resolution mass spectrometry for the determination of low molecular weight organic and inorganic anions

    Energy Technology Data Exchange (ETDEWEB)

    Gilchrist, Elizabeth S. [Analytical & Environmental Science Division, Department of Forensic & Analytical Science, King’s College London, 150 Stamford Street, London, SE1 9NH (United Kingdom); Nesterenko, Pavel N. [Australian Centre for Research on Separation Science, School of Physical Sciences, University of Tasmania, Private Bag 75, Hobart 7001 (Australia); Smith, Norman W. [Analytical & Environmental Science Division, Department of Forensic & Analytical Science, King’s College London, 150 Stamford Street, London, SE1 9NH (United Kingdom); Barron, Leon P., E-mail: leon.barron@kcl.ac.uk [Analytical & Environmental Science Division, Department of Forensic & Analytical Science, King’s College London, 150 Stamford Street, London, SE1 9NH (United Kingdom)

    2015-03-20

    Highlights: • IC selectivity at high contents of organic solvent in eluent and elevated temperature is studied. • Solvent-enhanced IC coupled to high resolution MS is beneficial for sensitive detection of ions. • The first application of IC-HRMS to the detection of low explosives in fingermarks is shown. - Abstract: There has recently been increased interest in coupling ion chromatography (IC) to high resolution mass spectrometry (HRMS) to enable highly sensitive and selective analysis. Herein, the first comprehensive study focusing on the direct coupling of suppressed IC to HRMS without the need for post-suppressor organic solvent modification is presented. Chromatographic selectivity and added HRMS sensitivity offered by organic solvent-modified IC eluents on a modern hyper-crosslinked polymeric anion-exchange resin (IonPac AS18) are shown using isocratic eluents containing 5–50 mM hydroxide with 0–80% methanol or acetonitrile for a range of low molecular weight anions (<165 Da). Comprehensive experiments on IC thermodynamics over a temperature range between 20–45 °C with the eluent containing up to 60% of acetonitrile or methanol revealed markedly different retention behaviour and selectivity for the selected analytes on the same polymer based ion-exchange resin. Optimised sensitivity with HRMS was achieved with as low as 30–40% organic eluent content. Analytical performance characteristics are presented and compared with other IC-MS based works. This study also presents the first application of IC-HRMS to forensic detection of trace low-order anionic explosive residues in latent human fingermarks.

  6. Isolation, purification and characterisation of an organic solvent-tolerant Ca2+-dependent protease from Bacillus megaterium AU02.

    Science.gov (United States)

    Priya, J Deepa Arul; Divakar, K; Prabha, M Suriya; Selvam, G Panneer; Gautam, Pennathur

    2014-01-01

    A new organic solvent-tolerant strain Bacillus megaterium AU02 which secretes an organic solvent-tolerant protease was isolated from milk industry waste. Statistical methods were employed to achieve optimum protease production of 43.6 U/ml in shake flask cultures. The productivity of the protease was increased to 53 U/ml when cultivated under controlled conditions in a 7-L fermentor. The protease was purified to homogeneity by a three-step process with 24 % yield and specific activity of 5,375 U/mg. The molecular mass of the protease was found to be 59 kDa. The enzyme was active over a wide range of pH (6.0–9.0), with an optimum activity at pH 7.0 and temperature from 40 to 70 °C having an optimum activity at 50 °C. The thermal stability of the enzyme increased significantly in the presence of CaCl2, and it retained 90 % activity at 50 °C for 3 h. The Km and Vmax values were determined as 0.722 mg/ml and 0.018 U/mg respectively. The metalloprotease exhibited significant stability in the presence of organic solvents with log P values more than 2.5, nonionic detergents and oxidising agent. An attempt was made to test the synthesis of aspartame precursor (Cbz-Asp-Phe-NH2) which was catalysed by AU02 protease in the presence of 50 % DMSO. These properties of AU02 protease make it an ideal choice for enzymatic peptide synthesis in organic media. PMID:24122712

  7. Effective clean-up of organic liquid contaminants including BTEX, fuels, and organic solvents from the environment by poly(alkoxysilane) sorbents.

    Science.gov (United States)

    Karadag, Koksal; Yati, Ilker; Bulbul Sonmez, Hayal

    2016-06-01

    Novel cross-linked poly(alkoxysilane)s, which can be used for the removal of organic liquid contaminants from water, were synthesized in one step, in a solvent free reaction medium, at moderately high temperature without using a catalyst. The synthesized polymers were characterized by Fourier transform infrared spectroscopy (FTIR), solid-state (13)C and (29)Si cross-polarization magic angle spinning (CPMAS) nuclear magnetic resonance (NMR), thermal gravimetric analysis (TGA) and differential scanning calorimetry (DSC) methods and elemental analysis. The swelling features of the poly(alkoxysilane)s were investigated in organic solvents and oils, such as dichloromethane, benzene, toluene, xylene, methyl tertiary butyl ether, and also some fuel derivatives, such as gasoline and euro diesel. All polymers have high-fast solvent uptake abilities, good reusability and thermal stability. The swelling features of the synthesized cross-linked polymers were evaluated by the swelling test, absorption-desorption kinetics. Thus, the results propose that cross-linked poly(alkoxysilane)s are suitable for the absorption of oil-organic pollutants from the water surface. PMID:26999646

  8. Solvents and Parkinson disease: A systematic review of toxicological and epidemiological evidence

    Energy Technology Data Exchange (ETDEWEB)

    Lock, Edward A., E-mail: e.lock@ljmu.ac.uk [Liverpool John Moores University, School of Pharmacy and Biomolecular Sciences, Byrom Street, Liverpool (United Kingdom); Zhang, Jing [University of Washington, Department of Pathology, School of Medicine, Seattle, WA (United States); Checkoway, Harvey [University of Washington, Department of Environmental and Occupational Health Sciences, Seattle, WA (United States)

    2013-02-01

    Parkinson disease (PD) is a debilitating neurodegenerative motor disorder, with its motor symptoms largely attributable to loss of dopaminergic neurons in the substantia nigra. The causes of PD remain poorly understood, although environmental toxicants may play etiologic roles. Solvents are widespread neurotoxicants present in the workplace and ambient environment. Case reports of parkinsonism, including PD, have been associated with exposures to various solvents, most notably trichloroethylene (TCE). Animal toxicology studies have been conducted on various organic solvents, with some, including TCE, demonstrating potential for inducing nigral system damage. However, a confirmed animal model of solvent-induced PD has not been developed. Numerous epidemiologic studies have investigated potential links between solvents and PD, yielding mostly null or weak associations. An exception is a recent study of twins indicating possible etiologic relations with TCE and other chlorinated solvents, although findings were based on small numbers, and dose–response gradients were not observed. At present, there is no consistent evidence from either the toxicological or epidemiologic perspective that any specific solvent or class of solvents is a cause of PD. Future toxicological research that addresses mechanisms of nigral damage from TCE and its metabolites, with exposure routes and doses relevant to human exposures, is recommended. Improvements in epidemiologic research, especially with regard to quantitative characterization of long-term exposures to specific solvents, are needed to advance scientific knowledge on this topic. -- Highlights: ► The potential for organic solvents to cause Parkinson's disease has been reviewed. ► Twins study suggests etiologic relations with chlorinated solvents and Parkinson's. ► Animal studies with TCE showed potential to cause damage to dopaminergic neurons. ► Need to determine if effects in animals are relevant to human

  9. Zinc isotope separation by phenol formaldehyde type 15-crown-5 resin in organic solvents

    International Nuclear Information System (INIS)

    Zinc adsorption and isotope separation by newly synthesized benzo-15-crown-5 resin was evaluated using various solvents. This resin was synthesized in the pores of silica beads for chromatography use. Larger adsorption of zinc was obtained in the case of acetic acid derivatives than in protic solvent such as water and alcohol by the batch treatment. The displacement chromatography was conducted to study zinc isotope separation. The isotope separation coefficient ε=0.32x10-3, 0.69x10-3 and HETP=0.2268, 0.3968 cm were determined for isotopic pair of 68Zn/64Zn at 25degC by five meters migration experiment using methyl isobutyl ketone and acetic acid, respectively. The improvement of enrichment ratio is very small between 1 and 5 m migration. Hydrogen chloride and/or water obviously reduce zinc adsorption to this resin. (author)

  10. Predicting the Disorder–Order Transition of Solvent-Free Nanoparticle–Organic Hybrid Materials

    KAUST Repository

    Yu, Hsiu-Yu

    2013-07-02

    The transition from a disordered to a face-centered-cubic phase in solvent-free oligomer-tethered nanoparticles is predicted using a density-functional theory for model hard spheres with tethered bead-spring oligomers. The transition occurs without a difference of volume fraction for the two phases, and the phase boundary is influenced by the loss of oligomer configurational entropy relative to an ideal random system in one phase compared with the other. When the particles are localized in the ordered phase, the cooperation of the oligomers in filling the space is hindered. Therefore, shorter oligomers feel a stronger entropic penalty in the ordered solid and favor the disordered phase. Strikingly, we found that the solvent-free system has a later transition than hard spheres for all investigated ratios of oligomer radius of gyration to particle radius. © 2013 American Chemical Society.

  11. A comparative study of room temperature ionic liquids and their organic solvent mixtures near charged electrodes

    Science.gov (United States)

    Vatamanu, Jenel; Vatamanu, Mihaela; Borodin, Oleg; Bedrov, Dmitry

    2016-11-01

    The structural properties of electrolytes consisting of solutions of ionic liquids in a polar solvent at charged electrode surfaces are investigated using classical atomistic simulations. The studied electrolytes consisted of tetraethylammonium tetrafluoroborate (NEt4-BF4), 1-ethyl-3-methylimidazolium tetrafluoroborate (c2mim-BF4) and 1-octyl-3-methylimidazolium tetrafluoroborate (c8mim-BF4) salts dissolved in acetonitrile solvent. We discuss the influence of electrolyte concentration, chemical structure of the ionic salt, temperature, conducting versus semiconducting nature of the electrode, electrode geometry and surface roughness on the electric double layer structure and capacitance and compare these properties with those obtained for pure room temperature ionic liquids. We show that electrolytes consisting of solutions of ions can behave quite differently from pure ionic liquid electrolytes.

  12. The solvent-extractable organic compounds in the Indonesia biomass burning aerosols - characterization studies

    Energy Technology Data Exchange (ETDEWEB)

    Fang, M.; Zheng, M.; Wang, F.; To, K.L. [The Hong Kong University of Science and Technology (Hong Kong). Applied Technology Center; Jaafar, A.B.; Tong, S.L. [Alam Sekitar Malaysia Sdn Bhd, Kuala Lumpur (Malaysia)

    1999-07-01

    The large-scale air pollution episode due to the out-of-control biomass burning for agricultural purposes in Indonesia started in June 1997, has become a severe environmental problem for itself and the neighboring countries. The fire lasted for almost five months. Its impact on the health and ecology in the affected areas is expected to be substantial, costly and possibly long lasting. Air pollution Index as high as 839 has been reported in Malaysia. API is calculated based on the five pollutants: NO{sub 2}, SO{sub 2}, O{sub 3}, CO, and respirable suspended particulates (PMIO). It ranges in value from 0 to 500. An index above 101 is considered to be unhealthy and a value over 201 is very unhealthy (Abidin and Shin, 1996). The solvent-extractable organic compounds from four total suspended particulate (TSP) high-volume samples collected in Kuala Lumpur, Malaysia (Stations Pudu and SIRIM) were subjected to characterization - the abundance was determined and biomarkers were identified. Two of the samples were from early September when the fire was less intense, while the other two were from late September when Kuala Lumpur experienced very heavy smoke coverage which could be easily observed from NOAA/AVHRR satellite images. The samples contained mainly aliphatic hydrocarbons such as n-alkanes and triterpanes, alkanoic acids, alkanols, and polycyclic aromatic hydrocarbons. The difference between the early and late September samples was very significant. The total yield increased from 0.6 to 24.3 {mu}g m{sup -3} at Pudu and 1.9 to 20.1 {mu}g m{sup -3} at SIRIM, with increases in concentration in every class. The higher input of vascular plant wax components in the late September samples, when the fire was more intense, was characterized by the distribution patterns of the homologous series n-alkanes, n-alkanoic acids, and n-alkanols, e.g., lower U:R, higher > C{sub 22} < C{sub 20} for n-alkanoic acids, higher > C{sub 20}/ < C{sub 20} for n-alkanols, a shift in C{sub max

  13. Determination of terpenoid content in pine by organic solvent extraction and fast-GC analysis

    Directory of Open Access Journals (Sweden)

    Anne Elizabeth Harman-Ware

    2016-01-01

    Full Text Available Terpenoids, naturally occurring compounds derived from isoprene units present in pine oleoresin, are a valuable source of chemicals used in solvents, fragrances, flavors and have shown potential use as a biofuel. This paper describes a method to extract and analyze the terpenoids present in loblolly pine saplings and pine lighter wood. Various extraction solvents were tested over different times and temperatures. Samples were analyzed by pyrolysis-molecular beam mass spectrometry before and after extractions to monitor the extraction efficiency. The pyrolysis studies indicated that the optimal extraction method used a 1:1 hexane/acetone solvent system at 22°C for 1 h. Extracts from the hexane/acetone experiments were analyzed using a low thermal mass modular accelerated column heater for fast-GC/FID analysis. The most abundant terpenoids from the pine samples were quantified, using standard curves, and included the monoterpenes, α- and β- pinene, camphene and δ-carene. Sesquiterpenes analyzed included caryophyllene, humulene and α-bisabolene. Diterpenoid resin acids were quantified in derivatized extractions, including pimaric, isopimaric, levopimaric, palustric, dehydroabietic, abietic and neoabietic acids.

  14. Impact of Organic Solvents and Environmental Pollutants on the Physiological Function in Petrol Filling Workers

    Directory of Open Access Journals (Sweden)

    V. Devender Reddy

    2008-09-01

    Full Text Available Long term exposure to solvents and air pollutants can lead to deleterious effects on respiratory, haematological and thyroid functioning. The aim of this study was to investigate whether chronic exposure to solvents like benzene and pollutants like carbon monoxide in petrol filling workers had adverse effect on blood parameters, thyroid and respiratory functions. The study group consisted of 42 healthy, non-smoker petrol filling workers, aged 20-50 years with work (exposure duration from 2-15 years while 36 healthy subjects of the same age group served as controls. Physical examination and measurement of pulmonary functions by portable electronic spirometer were performed. Complete blood pictures (CBP were determined by normal haematology lab procedure and hormones by Chemiluminescence immunoassay (CLIA light absorption techniques. There was a significant decrease in the lung volumes and capacities; the restrictive pattern was more prevalent in the workers when compared with the control groups. But in the workers exposed for long period (more than 10 years the restrictive pattern was changed to mixed pattern. A significant increase in haemoglobin (Hb (>16 mg % and red blood cells (RBC (5.4 million cells/mm3 were observed in workers with longer period of exposure when compared with the control subjects (14.483 mg% and 4.83 million cells/mm3 for Hb and RBC respectively. White blood cell count except eosinophils and platelets were significantly lower in workers compared to controls. Marked increase in the tetra iodothyroinine (T4, free thyroxine (T4F level and significant decrease in thyroid stimulating hormones (TSH, and tri-iodothyronine (T3 were observed between long term exposed and non – exposed groups. Till now researchers focused only on the effect of solvents in workers professionally exposed to solvents without considering the effect of concomittant air pollution. The result obtained from present study indicates that there is

  15. Fabrication of cost effective iron ore slime ceramic membrane for the recovery of organic solvent used in coke production

    Institute of Scientific and Technical Information of China (English)

    V.Singh; N.K.Meena; A.K.Golder; C.Das

    2016-01-01

    Improvement of coking properties of sub-bituminous coal (A) and bituminous coal (B) was done using blended organic solvents,namely,n-methyl-2-pyrrolidinone (NMP) and ethylenediamine (EDA).Various solvent blends were employed for the coal extraction under the total reflux condition.A low-cost ceramic membrane was fabricated using industrial waste iron ore slime of M/s TATA steel R&D,Jamshedpur (India) to separate out the dissolved coking fraction from the solvent-coal mixture.Membrane separations were carried out in a batch cell,and around 75 % recovered NMP was reused.The fractionated coal properties were determined using proximate and ultimate analyses.In the case of bituminous coal,the ash and sulfur contents were decreased by 99.3 % and 79.2 %,respectively,whereas,the carbon content was increased by 23.9 % in the separated coal fraction.Three different cleaning agents,namely deionized water,sodium dodecyl sulphate and NMP were used to regain the original membrane permeability for the reusing.

  16. Influence of Dissolved O2 in Organic Solvents on CuOEP Supramolecular Self-Assembly on Graphite.

    Science.gov (United States)

    Hao, Yibo; Weatherup, Robert S; Eren, Baran; Somorjai, Gabor A; Salmeron, Miquel

    2016-06-01

    The supramolecular self-assembly of copper(II) octaethylporphyrin (CuOEP) and octaethylporphyrin (H2OEP) on graphitic surfaces immersed in organic solvents (dichlorobenzene, dodecane) is studied using scanning tunneling microscopy (STM) and Raman spectroscopy. STM reveals that the self-assembled structure of CuOEP in 1,2-dichlorobenzene is significantly altered by dissolved oxygen within the solvent. Raman spectroscopy reveals that the presence of the oxygen alters the molecule-substrate interaction, which is attributed to the adsorption of oxygen on the Cu center of the CuOEP, which is facilitated by electron transfer from the graphitic surface. Such oxygen-induced changes are not observed for H2OEP, indicating that the metal center of CuOEP plays a critical role. When the solvent is dodecane, we find that solvation effects dominate. CuOEP adsorbed on graphitic surfaces provides a model system relevant to the study of the transport and activation of oxygen by enzymes and other complexes. PMID:27180868

  17. The role of exhaust ventilation systems in reducing occupational exposure to organic solvents in a paint manufacturing factory

    Directory of Open Access Journals (Sweden)

    Jafari Mohammad

    2008-01-01

    Full Text Available This paper presents the successful design and implementation of several exhaust ventilation systems in a paint manufacturing factory. The ventilation systems were designed based on American Conference of Governmental Industrial Hygienists recommendations. The duct works, fans, and other parts were made and mounted by local manufacturers. The concentrations of toluene and xylene as the common solvents used in paint mixing factories were measured to evaluate the role of ventilation systems in controlling the organic solvents. Occupational exposure to toluene and xylene as the major pollutants was assessed with and without applying ventilation systems. For this purpose, samples were taken from breathing zone of exposed workers using personal samples. The samples were analyzed using Occupational Safety and Health Administration analytical method No.12. The samples were quantified using gas chromatography. The results showed that the ventilation systems successfully controlled toluene and xylene vapors in workplace, air well below the recommended threshold limit value of Iran (44.49 and 97.73 ppm, respectively. It was also discovered that benzene concentration in workplace air was higher than its allowable concentrations. This could be from solvents impurities that require more investigations.

  18. Transformation of iopamidol during chlorination.

    Science.gov (United States)

    Wendel, Friedrich M; Lütke Eversloh, Christian; Machek, Edward J; Duirk, Stephen E; Plewa, Michael J; Richardson, Susan D; Ternes, Thomas A

    2014-11-01

    The transformation of the iodinated X-ray contrast media (ICM) iopamidol, iopromide, iohexol, iomeprol, and diatrizoate was examined in purified water over the pH range from 6.5 to 8.5 in the presence of sodium hypochlorite, monochloramine, and chlorine dioxide. In the presence of aqueous chlorine, only iopamidol was transformed. All other ICM did not show significant reactivity, regardless of the oxidant used. Chlorination of iopamidol followed a second order reaction, with an observed rate constant of up to 0.87 M(-1) s(-1) (±0.021 M(-1) s(-1)) at pH 8.5. The hypochlorite anion was identified to be the reactive chlorine species. Iodine was released during the transformation of iopamidol, and was mainly oxidized to iodate. Only a small percentage (less than 2% after 24 h) was transformed to known organic iodinated disinfection byproducts (DBPs) of low molecular weight. Some of the iodine was still present in high-molecular weight DBPs. The chemical structures of these DBPs were elucidated via MSn fragmentation and NMR. Side chain cleavage was observed as well as the exchange of iodine by chlorine. An overall transformation pathway was proposed for the degradation of iopamidol. CHO cell chronic cytotoxicity tests indicate that chlorination of iopamidol generates a toxic mixture of high molecular weight DBPs (LC50 332 ng/μL).

  19. Methods for determination and analysis of gold, silver, and palladium on the basis of solvent extraction with organic sulfides

    International Nuclear Information System (INIS)

    A review of previously published and new data on the use of solvent extraction by organic sulfides in analytical chemistry of gold, silver and palladium is given. The consideration is made on the basis of close relation between ways of preliminary concentration of the element and peculiarities of the instrumental method of analysis used. Advantages of organic sulfides as extractants of gold, silver and palladium complexes, permitting to increase-considerably the factor of extraction purification from other metals without noticeable loss of the elements isolated, are pointed out. Comparison of metrological characteristics (the range of the contents determined, determination limit and relative standard deviation) of atomic-absorption, atomic-emission and neutron-activation methods of gold, silver and palladium determination with their preliminary extraction concentrating by organic sulfides is made. 70 refs.; 3 figs.; 7 tabs

  20. Glycosidic moiety changes the spectroscopic properties of DL-α-tocopherol in DMSO/water solution and in organic solvents

    Science.gov (United States)

    Neunert, G.; Polewski, P.; Walejko, P.; Markiewicz, M.; Witkowski, S.; Polewski, K.

    2009-07-01

    In this study we estimated how conjugation with a sugar moiety influences the spectral properties of tocopherol and relate the spectroscopic properties of glycosides to solvent properties such as viscosity and polarity. Spectroscopic properties (absorption, fluorescence, fluorescence anisotropy and fluorescence lifetime) of three DL-α-tocopheryl glycosides (DL-α-tocopheryl orthoacetate derivative and glycosides of DL-α-tocopherol model compounds: 2,2,5,7,8-pentamethyl-6-chromanol and Trolox) were studied in DMSO/water solution. In all investigated compounds dissolved in DMSO/water mixture the absorption and emission maxima were blue-shifted. The fluorescence lifetimes were longer compared with those obtained for the parent compounds, except for the Trolox glucoside, in which it was shorter. The observed effect is connected with an increase in the electronic energy in the ground state due to electron rearrangement in the chromanol system caused by interaction with the sugar moiety. The extent of the spectral shift is related to the sugar moiety substituted at the phenolic oxygen rather than to substitution at the 2a position in the chromanol ring. The fluorescent properties of DL-α-tocopheryl glucoside in organic solvents were measured. The Stokes shift was related to the orientational polarizability of the solvents. The study of viscosity suggested two different mechanisms explaining the results observed in a low- and high-viscosity environment. The results indicated the fundamental role of interactions between the chromophore and sugar moiety in a low-viscosity environment. The results obtained at high values of viscosity are discussed in terms of a frictional boundary solvent-solute interaction model.

  1. Effects of Polar Organic Solvent on Separation of Y(edta)-/Nd(edta)- Complexes on Polyacrylic Anion Exchangers

    Institute of Scientific and Technical Information of China (English)

    Halina Hubicka; Dorota Kolodynska

    2005-01-01

    The use of polar organic solvents for the separations of rare earth elements (Ⅲ) is effective especially for their extensive separations despite the solubility limitations. The study shows that polyacrylate anion exchangers, particularly the weakly basic, gel anion exchanger Amberlite IRA 68, can be applied to the separation of rare earth complexes with EDTA in H2O-methanol and H2O-ethanol systems. In most cases the determined distribution coefficients of Ln3+ complexes with EDTA in mixed media like water-methanol on polyacrylate anion exchangers are larger than those in pure water media.

  2. Identification, Characterization, and Immobilization of an Organic Solvent-Stable Alkaline Hydrolase (PA27) from Pseudomonas aeruginosa MH38

    OpenAIRE

    Eunjin Jang; Bum Han Ryu; Thomas Doohun Kim

    2014-01-01

    An organic solvent-stable alkaline hydrolase (PA27) from Pseudomonas aeruginosa MH38 was expressed, characterized, and immobilized for biotechnological applications. Recombinant PA27 was expressed in Escherichia coli as a 27 kDa soluble protein and was purified by standard procedures. PA27 was found to be stable at pH 8–11 and below 50 °C. It maintained more than 80% of its activity under alkaline conditions (pH 8.0–11.0). Furthermore, PA27 exhibited remarkable stability in benzene and n-hex...

  3. Solvent-Assisted Gel Printing for Micropatterning Thin Organic-Inorganic Hybrid Perovskite Films.

    Science.gov (United States)

    Jeong, Beomjin; Hwang, Ihn; Cho, Sung Hwan; Kim, Eui Hyuk; Cha, Soonyoung; Lee, Jinseong; Kang, Han Sol; Cho, Suk Man; Choi, Hyunyong; Park, Cheolmin

    2016-09-27

    While tremendous efforts have been made for developing thin perovskite films suitable for a variety of potential photoelectric applications such as solar cells, field-effect transistors, and photodetectors, only a few works focus on the micropatterning of a perovskite film which is one of the most critical issues for large area and uniform microarrays of perovskite-based devices. Here we demonstrate a simple but robust method of micropatterning a thin perovskite film with controlled crystalline structure which guarantees to preserve its intrinsic photoelectric properties. A variety of micropatterns of a perovskite film are fabricated by either microimprinting or transfer-printing a thin spin-coated precursor film in soft-gel state with a topographically prepatterned elastomeric poly(dimethylsiloxane) (PDMS) mold, followed by thermal treatment for complete conversion of the precursor film to a perovskite one. The key materials development of our solvent-assisted gel printing is to prepare a thin precursor film with a high-boiling temperature solvent, dimethyl sulfoxide. The residual solvent in the precursor gel film makes the film moldable upon microprinting with a patterned PDMS mold, leading to various perovskite micropatterns in resolution of a few micrometers over a large area. Our nondestructive micropatterning process does not harm the intrinsic photoelectric properties of a perovskite film, which allows for realizing arrays of parallel-type photodetectors containing micropatterns of a perovskite film with reliable photoconduction performance. The facile transfer of a micropatterned soft-gel precursor film on other substrates including mechanically flexible plastics can further broaden its applications to flexible photoelectric systems.

  4. Ultrasonic measurements and other allied parameters of yttrium soaps in mixed organic solvents

    International Nuclear Information System (INIS)

    The ultrasonic measurements of yttrium soaps were made in a mixture of 70 % benzene and 30 % dimethylsulfoxide (ν/ν) to determine the critical micelle concentration, soap-solvent interaction and various acoustic and thermodynamic parameters. The values of the CMC decrease with increasing chainlength of fatty acid constituent of the soap molecule and are in agreement with the values obtained from other micellar properties. The various acoustic parameters (intermolecular freelength, adiabatic compressibility, apparent molar compressibility, specific acoustic impedance, apparent molar volume, molar sound velocity, solvation number, available volume and relative association) for yttrium soaps (myristate, palmitate, stearate and oleate) have been evaluated by ultrasonic velocity measurements. (Authors)

  5. Predispersed solvent extraction

    OpenAIRE

    Rodarte, Alma Isabel Marín

    1988-01-01

    A new solvent extraction method has been developed for the extraction of metal and organic ions from very dilute aqueous solutions. The new method, which has been named Predispersed Solvent Extraction (POSE), is based on the principle that 1 there is no need to comminute both phases. All that is necessary is to comminute the solvent phase prior to contacting it with the feed. This is done by converting the solvent into aphrons, which are micron-sized globules encapsulated in a ...

  6. Chlorinated indium tin oxide electrode by InCl3 aqueous solution for high-performance organic light-emitting diodes

    Science.gov (United States)

    Hu, Yun; Zhou, Dong-Ying; Wang, Bo; Wang, Zhao-Kui; Liao, Liang-Sheng

    2016-04-01

    The authors develop a facile and effective method to produce the chlorinated indium tin oxide (Cl-ITO) treated by InCl3 aqueous solution and UV/ozone. The work function of the Cl-ITO achieved by this treatment is as high as 5.69 eV, which is increased by 1.09 eV compared with that of the regular ITO without any treatment. Further investigation proved that the enhancement of the work function is attributed to the formation of In-Cl bonds on the Cl-ITO surface. Green phosphorescent organic light-emitting devices based on the Cl-ITO electrodes exhibit excellent electroluminescence performance, elongating lifetime due to the improvement in hole injection.

  7. In Situ and Laboratory Studies on the Fate of Specific Organic Compounds in an Anerobic Landfill Leachate Plume, 2. Fate of Aromatic and Chlorinated Aliphatic Compounds

    DEFF Research Database (Denmark)

    Nielsen, Per Henning; Bjarnadóttir, Helga; Winter, Pia L.;

    1995-01-01

    and laboratory batch microcosm experiments performed focusing on redox conditions, microbiology and the fate of 7 phenolic compounds. In this paper we present the results on the fate of 8 aromatic compounds and 4 chlorinated aliphatic compounds. Nitrobenzene was transformed at all distances from the landfill......The transformation of specific organic compounds was investigated by in situ and laboratory experiments in an anaerobic landfill leachate pollution plume at four different distances from the landfill. In a previous paper (Part 1, also published in this issue) we described the in situ microcosm...... the landfill. In general, good accordance with respect to compound transformation was observed between in situ and laboratory experiments, but in a few cases more compounds were transformed in in situ experiments than in the corresponding laboratory experiments....

  8. One novel multidimensional organic-inorganic hybrid based on polyoxometalates and copper chlorine coordination polymers with 4,4′-bipyridine ligands

    Institute of Scientific and Technical Information of China (English)

    Li Chun Xuan; Qing Jiang Pan

    2012-01-01

    One novel organic-inorganic hybrid materials with 4,4′-bipy ligands and copper chlorine coordination polymers as linkers,with new topology,{[CuI(4,4′-bipy)]10Cl2(SiW12O40)2}·6H2O (1) (4,4′-bipy =4,4′-bipyridine),has been hydrothermally synthesized.The single crystal X-ray structural analysis reveals that the structure of 1 is constructed from classical Keggin anions and [CuI(4,4′-bipy)] cations into a novel,three-dimensional (3D) polyoxometalates (POMs)based network.From the topological view,compound 1 is a novel (3.44.52.63)(32.44.56.69) topology.The electrochemical and photocatalysis properties of 1 have been investigated in details.

  9. Esterase Active in Polar Organic Solvents from the Yeast Pseudozyma sp. NII 08165

    Directory of Open Access Journals (Sweden)

    Deepthy Alex

    2014-01-01

    Full Text Available Esterases/lipases active in water miscible solvents are highly desired in biocatalysis where substrate solubility is limited and also when the solvent is desired as an acyl acceptor in transesterification reactions, as with the case of biodiesel production. We have isolated an esterase from the glycolipid producing yeast-Pseudozyma sp. NII 08165 which in its crude form was alkali active, thermo stable, halo tolerant and also capable of acting in presence of high methanol concentration. The crude enzyme which maintained 90% of its original activity after being treated at 70°C was purified and the properties were characterized. The partially purified esterase preparation had temperature and pH optima of 60°C and 8.0 respectively. The enzyme retained almost complete activity in presence of 25% methanol and 80% activity in the same strength of ethanol. Conditions of enzyme production were optimized, which lead to 9 fold increase in the esterase yield. One of the isoforms of the enzyme LIP1 was purified to homogeneity and characterized. Purified LIP1 had a Km and Vmax of 0.01 and 1.12, respectively. The purified esterase lost its thermo and halo tolerance but interestingly, retained 97% activity in methanol.

  10. Preliminary assessment of microbial communities and biodegradation of chlorinated volatile organic compounds in wetlands at Cluster 13, Lauderick Creek area, Aberdeen Proving Ground, Maryland

    Science.gov (United States)

    Lorah, Michelle M.; Voytek, Mary A.; Spencer, Tracey A.

    2003-01-01

    A preliminary assessment of the microbial communities and biodegradation processes for chlorinated volatile organic compounds was con-ducted by the U.S. Geological Survey in wetlands at the Cluster 13, Lauderick Creek area at Aberdeen Proving Ground, Maryland. The U.S. Geological Survey collected wetland sediment samples from 11 sites in the Lauderick Creek area for microbial analyses, and used existing data to evaluate biodegradation processes and rates. The bacterial and methanogen communities in the Lauderick Creek wetland sediments were similar to those observed in a previous U.S. Geological Survey study at the West Branch Canal Creek wet-land area, Aberdeen Proving Ground. Evaluation of the degradation rate of 1,1,2,2-tetrachloroethane and the daughter compounds produced also showed similar results for the two wetlands. How-ever, a vertical profile of contaminant concentra-tions in the wetlands was available at only one site in the Lauderick Creek area, and flow velocities in the wetland sediment are unknown. To better evaluate natural attenuation processes and rates in the wetland sediments at Lauderick Creek, chemi-cal and hydrologic measurements are needed along ground-water flowpaths in the wetland at additional sites and during different seasons. Nat-ural attenuation in the wetlands, enhanced biore-mediation, and constructed wetlands could be feasible remediation methods for the chlorinated volatile organic compounds discharging in the Lauderick Creek area. The similarities in the microbial communities and biodegradation pro-cesses at the Lauderick Creek and West Branch Canal Creek areas indicate that enhanced bioreme-diation techniques currently being developed for the West Branch Canal Creek wetland area would be transferable to this area.

  11. Production, Optimization, and Characterization of Organic Solvent Tolerant Cellulases from a Lignocellulosic Waste-Degrading Actinobacterium, Promicromonospora sp. VP111.

    Science.gov (United States)

    Thomas, Lebin; Ram, Hari; Kumar, Alok; Singh, Ved Pal

    2016-07-01

    High costs of natural cellulose utilization and cellulase production are an industrial challenge. In view of this, an isolated soil actinobacterium identified as Promicromonospora sp. VP111 showed potential for production of major cellulases (CMCase, FPase, and β-glucosidase) utilizing untreated agricultural lignocellulosic wastes. Extensive disintegration of microcrystalline cellulose and adherence on it during fermentation divulged true cellulolytic efficiency of the strain. Conventional optimization resulted in increased cellulase yield in a cost-effective medium, and the central composite design (CCD) analysis revealed cellulase production to be limited by cellulose and ammonium sulfate. Cellulase activities were enhanced by Co(+2) (1 mM) and retained up to 60 °C and pH 9.0, indicating thermo-alkaline tolerance. Cellulases showed stability in organic solvents (25 % v/v) with log P ow  ≥ 1.24. Untreated wheat straw during submerged fermentation was particularly degraded and yielded about twofold higher levels of cellulases than with commercial cellulose (Na-CMC and avicel) which is especially economical. Thus, this is the first detailed report on cellulases from an efficient strain of Promicromonospora that was non-hemolytic, alkali-halotolerant, antibiotic (erythromycin, kanamycin, rifampicin, cefaclor, ceftazidime) resistant, multiple heavy metal (Mo(+6) = W(+6) > Pb(+2) > Mn(+2) > Cr(+3) > Sn(+2)), and organic solvent (n-hexane, isooctane) tolerant, which is industrially and environmentally valuable. PMID:26956574

  12. Accelerated solvent extraction (ASE) for purification and extraction of silicone passive samplers used for the monitoring of organic pollutants.

    Science.gov (United States)

    Brockmeyer, Berit; Kraus, Uta R; Theobald, Norbert

    2015-12-01

    Silicone passive samplers have gained an increasing attention as single-phased, practical and robust samplers for monitoring of organic contaminants in the aquatic environment in recent years. However, analytical challenges arise in routine application during the extraction of analytes as silicone oligomers are co-extracted and interfere severely during chemical analyses (e.g. gas chromatographic techniques). In this study, we present a fast, practical pre-cleaning method for silicone passive samplers applying accelerated solvent extraction (ASE) for the removal of silicone oligomers prior to the water deployment (hexane/dichloromethane, 100 °C, 70 min). ASE was also shown to be a very fast (10 min) and efficient extraction method for non-polar contaminants (non-exposed PRC recoveries 66-101 %) sampled by the silicone membrane. For both applications, temperature, extraction time and the solvent used for ASE have been optimized. Purification of the ASE extract was carried out by silica gel and high-pressure liquid size exclusion chromatography (HPLC-SEC). The silicone oligomer content was checked by total reflection X-ray fluorescence spectroscopy (TXRF) in order to confirm the absence of the silicone oligomers prior to analysis of passive sampler extracts. The established method was applied on real silicone samplers from the North- and Baltic Sea and showed no matrix effects during analysis of organic pollutants. Internal laboratory standard recoveries were in the same range for laboratory, transport and exposed samplers (85-126 %). PMID:26289330

  13. Effect of Organic Solvents in Preparation of Silica-Based Chemical Gel Decontaminates for Decontamination of Nuclear Facilities

    International Nuclear Information System (INIS)

    Decontamination of nuclear facilities is necessary to reduce the radiation field during normal operations and decommissioning of complex equipment such as stainless steel components, other iron-based steel and alloys, metal surfaces, structural materials and so on. Chemical decontamination technology in particular is a highly effective method to remove the radioactive contamination through a chemical dissolution or a redox reaction. However, this method has the serious drawback due to the generation of large amounts of the radioactive liquid wastes. Recently, a few literatures have been reported for the preparation of the chemical gel decontaminants to reduce the amount of the radioactive liquid wastes and to enhance the decontamination efficiency through increasing the contact time between the gels and the radioactive contaminants. In the preparation of the chemical gels, the control of the viscosity highly depends on the amount of a coviscosifier used among the components of the chemical gels consisted of a viscosifier, a coviscosifier, and a chemical decontaminant. In this works, a new effective method for the preparation of the chemical gel was investigated by introducing the organic solvents. The mixture solution of the coviscosifier and organic solvent was more effective in the control of the viscosity compared with that of the coviscosifier only in gels. Furthermore, the decontamination efficiency of the chemical gels measured by using the multi-channel analyzer (MCA) showed the high decontamination factor for Co-60 and Cs-137 contaminated on the surface of the stainless steel 304

  14. Laser photolysis study of anthraquinone in binary mixtures ofionic liquid [bmim][PF6] and organic solvent

    Directory of Open Access Journals (Sweden)

    Side Yao

    2006-12-01

    Full Text Available Photochemical properties of the ionic liquid (RTIL 1-butyl-3-methylimidazoliumhexafluorophosphate [bmim][PF6] and its binary mixed solutions with organic solvent(DMF and MeCN were investigated by laser photolysis at an excitation wavelength of 355nm, using anthraquinone (AQ as a probe molecule. It was indicated that the triplet excitedstate of AQ (3AQ* can abstract hydrogen from [bmim][PF6]. Moreover, along with thechange of the ratio of RTIL and organic solvent, the reaction rate constant changes regularly.Critical points were observed at volume fraction VRTIL = 0.2 for RTIL/MeCN and VRTIL =0.05 for RTIL/DMF. For both systems, before the critical point, the rate constant increasesrapidly with increasing VRTIL; however, it decreases obviously with VRTIL after the criticalpoint. We conclude that the concentration dependence is dominant at lower VRTIL, while theviscosity and phase transformation are dominant at higher VRTIL for the effect of ionic liquidon the decay of rate constant.

  15. H-bonding-directed self-assembly of synthetic copolymers containing nucleobases: organization and colloidal fusion in a noncompetitive solvent.

    Science.gov (United States)

    Lutz, Jean-François; Pfeifer, Sebastian; Chanana, Munish; Thünemann, Andreas F; Bienert, Ralf

    2006-08-15

    The self-organization of random copolymers composed of a nucleobase monomer (either 1-(4-vinylbenzyl)thymine or 9-(4-vinylbenzyl)adenine) and dodecyl methacrylate (DMA) was studied in dilute chloroform solutions. The balance between the molar fractions of the nucleobase monomer (leading to intermolecular H-bonding) and DMA (soluble moiety in chloroform) in the polymer chains was found to be the parameter that principally influences the self-organization. DMA-rich copolymers are molecularly soluble in chloroform, whereas nucleobase-rich copolymers are insoluble in this solvent. Copolymers possessing an equimolar comonomer composition self-assemble into micrometer-sized particles physically cross-linked by intermolecular H-bonds (either thymine-thymine or adenine-adenine interactions, depending on the studied copolymer). Nevertheless, when mixed together, thymine- and adenine-based colloids fuse into thermodynamically stable microspheres cross linked by adenine-thymine interactions.

  16. Comparative evaluation of effects of ozonated and chlorinated thermal discharges on estuarine and fresh water organisms. First quarterly progress report, April 1979

    Energy Technology Data Exchange (ETDEWEB)

    Guerra, C.R.; DelMonaco, J.L.; Singletary, J.H.; Sugam, R.J.; Meldrim, J.W.; Holmstrom, E.R.; Balog, G.F.

    1979-01-01

    The biological evaluation program incorporates three types of experimental tests: acute (96 hour) toxicity studies; behavioral (avoidance) response studies; and physiological (cough) response studies. In addition, specimens used in testing are examined for physical damage resulting from exposure to chlorine or ozoen. The objective of the acute (96 hour) toxicity study is to determine the respective lethal levels (LC/sub 50/) of chlorinated and ozonated waters. The objective of the behavioral (avoidance) response study is to determine what (if any) concentrations of ozone and of chlorine will be avoided. The objective of physiological (cough) response study is to determine what concentrations of ozone and of chlorine are physiologically detected. Ozonated and chlorinated waters were evaluated in all studies for both the addition of increased temperature and without it. Results indicate that ozone is less toxic than chlorine under the test conditions used. The lethal levels vary according to species of water quality measurements at Bergen Generating Station, New York are tabulated. (JBG)

  17. Studies on the Surface Interaction and Dispersity of Silver Nanoparticles in Organic Solvents

    Institute of Scientific and Technical Information of China (English)

    ZENG Rong; RONG Min-Zhi; ZHANG Ming-Qiu; ZENG Han-Min

    2000-01-01

    Silver nanoparticles with different sizes have been prepared by microemulsion and have been surface-modified with C12H25SH. Electron spin resonance results indicate that there exist some kinds of surface local paramagnetic sites in capped Ag nanoparticles, which leads to the relation between electron spin resonance parameters and particle size deviating from Kawabata's description. Thereis a strong interaction between nanosilver and chloroform. The smaller the particles, the stronger the interaction. Transmission electron microscopy and ultravilolet-visible absorption spectra confirmed that Ag nanoparticles are well dispersed in chloroform, implying that a good dispersity of Ag nanoparticles in polymers could be obtained by means of solution mixing by using chloroform as the solvent.

  18. Two-stage dilute-acid and organic-solvent lignocellulosic pretreatment for enhanced bioprocessing

    Energy Technology Data Exchange (ETDEWEB)

    Brodeur, G.; Telotte, J.; Stickel, J. J.; Ramakrishnan, S.

    2016-11-01

    A two stage pretreatment approach for biomass is developed in the current work in which dilute acid (DA) pretreatment is followed by a solvent based pretreatment (N-methyl morpholine N oxide -- NMMO). When the combined pretreatment (DAWNT) is applied to sugarcane bagasse and corn stover, the rates of hydrolysis and overall yields (>90%) are seen to dramatically improve and under certain conditions 48 h can be taken off the time of hydrolysis with the additional NMMO step to reach similar conversions. DAWNT shows a 2-fold increase in characteristic rates and also fractionates different components of biomass -- DA treatment removes the hemicellulose while the remaining cellulose is broken down by enzymatic hydrolysis after NMMO treatment to simple sugars. The remaining residual solid is high purity lignin. Future work will focus on developing a full scale economic analysis of DAWNT for use in biomass fractionation.

  19. Miscible Organic Solvents Soak Bonding Method Use in a PMMA Multilayer Microfluidic Device

    Directory of Open Access Journals (Sweden)

    He Zhang

    2014-12-01

    Full Text Available In this paper, we proposed a novel bonding technology to fabricate a microfluidic device based on Poly(methyl methacrylate (PMMA. The method, which used chloroform and ethanol as miscible bonding solvent, can complete complex structures rapid assembly (10 min at 40°C. A bonding strength of 267.5 N/cm2 can be achieved, while the micro channel deformation was less than 7.26%. Then we utilized this method to produce a three layers micro mixer, which included a T-shaped inlet channel and six H-shaped mixing units. Numerical simulation indicated that, the well mixing length of the mixer was only about 6 mm when Re = 10. Finally, fluorescence microscopy was used to verify mixer performance. The method provided the potential for mass production of multilayer rigid polymer microfluidic devices.

  20. Enzymatic Lipophilization of Phenolic Acids through Esterification with Fatty Alcohols in Organic Solvents

    DEFF Research Database (Denmark)

    Yang, Zhiyong; Guo, Zheng; Xu, Xuebing

    2012-01-01

    the volume ratio from 85:15 to 45:55. It was found that the conversion strongly depended on the proportion of hexane and butanone in the reaction system. Following the effect of carbons of fatty alcohol chains on estererification performance with dihydrocaffeic acid (DHCA) was evaluated by choosing different......In this study, we investigated and optimized the synthesis of lipophilized esters between selected phenolic acids and fatty alcohols in a binary solvent system, which is composed of hexane and butanone. The effect of different proportion of hexane and butanone was firstly studied by changing...... fatty alcohols from C4 to C18. The conversion of DHCA was significantly affected by the carbons of fatty alcohol chains. Roughly 95% conversion was achieved within 3 days when DHCA was esterified with hexanol (C6), while only 56% and 44% conversion were achieved when esterified with 1-butanol...