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Sample records for accelerated solvent extraction

  1. Factors affecting high-pressure solvent extraction (accelerated solvent extraction) of additives from polymers.

    Science.gov (United States)

    Vandenburg, H J; Clifford, A A; Bartle, K D; Zhu, S A; Carroll, J; Newton, I D; Garden, L M

    1998-05-01

    Irganox 1010 (pentaerythritol tetrakis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)] propionate) is successfully extracted from polypropylene using solvents at high temperatures and pressures in a homemade accelerated solvent extraction system. For example, using freeze-ground polymer, 90% extraction is possible within 5 min with 2-propanol at 150 °C. Extraction curves for 2-propanol and acetone fit well to the "hot ball" model, previously developed for supercritical fluid extraction. Diffusion coefficients are determined for extractions with 2-propanol, acetone, and cyclohexane over a range of temperatures, and the activation energies for the diffusion are 134, 107, and 61 kJ mol(-)(1), respectively. The lower figure for acetone and cyclohexane indicates that these solvents swell the polymer more than does 2-propanol. The polymer dissolves in the solvent at too high a temperature, which causes blockage of the transfer lines. For maximum extraction rates, the highest temperature for each solvent that avoids dissolution of the polymer should be used. The use of mixed solvents is investigated and shows advantages in some cases, with the aim of producing a solvent that will swell the polymer but not dissolve it.

  2. Accelerated solvent extraction of lignin from Aleurites moluccana (Candlenut) nutshells.

    Science.gov (United States)

    Klein, Andrew P; Beach, Evan S; Emerson, John W; Zimmerman, Julie B

    2010-09-22

    Lignin from candlenut shells was isolated using an ethanol-water accelerated solvent extraction method. Yields (based on Klason lignin) increased from about 14 to 33% as temperature increased from 100 to 195 °C and were also influenced by the amount of aqueous acid used to precipitate lignin from the extraction liquor. These yields were higher than could be obtained using a conventional dioxane-water acidolysis method. The resulting lignin was characterized by IR, 31P NMR, and 1H-13C HMQC NMR spectroscopic techniques. The lignin contained predominantly guaiacyl units, and both the total hydroxyl group content and phenolic hydroxyl group content were high.

  3. Extraction of Organochlorine Pesticides in Sediments Using Soxhlet, Ultrasonic and Accelerated Solvent Extraction Techniques

    Institute of Scientific and Technical Information of China (English)

    LANG Yinhai; CAO Zhengmei; NIE Xinhua

    2005-01-01

    The application of soxhlet, ultrasonic and accelerated solvent extraction techniques to the analysis of six organochlorine pesticides (α-HCH, β-HCH, γ-HCH, o, p'-DDT, p, p'-DDT and p, p'-DDE) in Taihu Lake sediment samples is described. It was found that the limits of quantification ranged from 0.002 μg g-1 to 0.004 μg g-1, and the recoveries of organochlorine pesticides with the three extraction techniques were acceptable (> 80.7%). With a mass selective detector,better results were obtained by accelerated solvent extraction using hexane-acetone (1: 1) as compared with soxhlet and ultrasonic extraction. It was shown that the accelerated solvent extraction was the optimum technique for the analysis of organochlorine pesticides in sediments. The general features of the three extraction techniques are also presented.

  4. The applicability of Accelerated Solvent Extraction (ASE) to extract lipid biomarkers from soils

    NARCIS (Netherlands)

    B. Jansen; K.G.J. Nierop; M.C. Kotte; P. de Voogt; J.M. Verstraten

    2006-01-01

    We investigated the ability of accelerated solvent extraction (ASE) to extract selected lipid biomarkers (C-19=C-34 n-alkanes, n-alcohols and n-fatty acids as well as dehydroabietic acid and P-sitosterol) from a sandy soil profile under Corsican pine. Two organic layers (moss and F1) as well as two

  5. Extraction of lignite coal fly ash for polynuclear aromatic hydrocarbons: modified and unmodified supercritical fluid extraction, enhanced-fluidity solvents, and accelerated solvent extraction.

    Science.gov (United States)

    Kenny, D V; Olesik, S V

    1998-02-01

    A comparison among modified and unmodified supercritical fluid extraction (SFE), enhanced-fluidity liquid extraction, and accelerated solvent extraction (ASE) techniques was made for the extraction of polynuclear aromatic hydrocarbons (PAHs) from an aged, spiked lignite coal fly ash. All of the attempted extraction conditions allowed the extraction of the PAHs to some degree, but no single extraction technique proved to be superior for all of the PAHs used. Three groups of PAHs with similar extraction efficiencies were identified. The group with the lowest molecular weights was best recovered using a 90% CO2-10% methanol mixture at 70 degrees C and 238 atm. The group of medium-molecular-weight PAHs was recovered equally well using any of three extraction conditions: SFE (100% CO2, 90 degrees C, and 238 atm), enhanced-fluidity liquid mixture (60% CO2-40% methanol, 70 degrees C, and 238 atm), and a methanol ASE mixture. The group of high-molecular-weight PAHs seemed to be equally well recovered with all of the attempted extraction conditions, but the enhanced-fluidity conditions (60% CO2-40% methanol, 70 degrees C, and 238 atm) had extraction recoveries (> 85%) with the lowest standard deviations (approximately 5%).

  6. Response Surface Modeling and Optimization of Accelerated Solvent Extraction of Four Lignans from Fructus Schisandrae

    Directory of Open Access Journals (Sweden)

    Jian Liang

    2012-03-01

    Full Text Available A new method based on accelerated solvent extraction (ASE combined with response surface methodology (RSM modeling and optimization has been developed for the extraction of four lignans in Fructus Schisandrae (the fruits of Schisandra chinensis Baill. The RSM method, based on a three level and three variable Box-Behnken design (BBD, was employed to obtain the optimal combination of extraction condition. In brief, the lignans schizandrin, schisandrol B, deoxyschizandrin and schisandrin B were optimally extracted with 87% ethanol as extraction solvent, extraction temperature of 160 °C, static extraction time of 10 min, extraction pressure of 1,500 psi, flush volume of 60% and one extraction cycle. The 3D response surface plot and the contour plot derived from the mathematical models were applied to determine the optimal conditions. Under the above conditions, the experimental value of four lignans was 14.72 mg/g, which is in close agreement with the value predicted by the model.

  7. Accelerated, microwave-assisted, and conventional solvent extraction methods affect anthocyanin composition from colored grains.

    Science.gov (United States)

    Abdel-Aal, El-Sayed M; Akhtar, Humayoun; Rabalski, Iwona; Bryan, Michael

    2014-02-01

    Anthocyanins are important dietary components with diverse positive functions in human health. This study investigates effects of accelerated solvent extraction (ASE) and microwave-assisted extraction (MAE) on anthocyanin composition and extraction efficiency from blue wheat, purple corn, and black rice in comparison with the commonly used solvent extraction (CSE). Factorial experimental design was employed to study effects of ASE and MAE variables, and anthocyanin extracts were analyzed by spectrophotometry, high-performance liquid chromatography-diode array detector (DAD), and liquid chromatography-mass spectrometry chromatography. The extraction efficiency of ASE and MAE was comparable with CSE at the optimal conditions. The greatest extraction by ASE was achieved at 50 °C, 2500 psi, 10 min using 5 cycles, and 100% flush. For MAE, a combination of 70 °C, 300 W, and 10 min in MAE was the most effective in extracting anthocyanins from blue wheat and purple corn compared with 50 °C, 1200 W, and 20 min for black rice. The anthocyanin composition of grain extracts was influenced by the extraction method. The ASE extraction method seems to be more appropriate in extracting anthocyanins from the colored grains as being comparable with the CSE method based on changes in anthocyanin composition. The method caused lower structural changes in anthocaynins compared with the MAE method. Changes in blue wheat anthocyanins were lower in comparison with purple corn or black rice perhaps due to the absence of acylated anthocyanin compounds in blue wheat. The results show significant differences in anthocyanins among the 3 extraction methods, which indicate a need to standardize a method for valid comparisons among studies and for quality assurance purposes.

  8. Extraction of bituminous coal fly ash for polynuclear aromatic hydrocarbons: evaluation of modified and unmodified supercritical fluid extraction, enhanced fluidity solvents, and accelerated solvent extraction.

    Science.gov (United States)

    Kenny, D V; Olesik, S V

    1998-02-01

    A comparison among supercritical fluid extraction (SFE), modified SFE, enhanced-fluidity extraction, and accelerated solvent extraction (ASE) techniques was made for the extraction of polynuclear aromatic hydrocarbons (PAHs) from an aged, spiked bituminous coal fly ash. Non-ASE extraction techniques used in this study could not recover PAHs with molecular weights greater than that of pyrene. ASE techniques using methylene chloride (with and without a static step) and toluene were able to recover most of the PAHs studied. None of the ASE techniques could quantitatively extract the low-molecular-weight PAHs from the bituminous fly ash. The medium-molecular-weight PAHs were best recovered with toluene ASE. The high-molecular-weight PAHs were best recovered with the toluene ASE technique (> 80%), but the overall precision of these measurements was low. Methylene chloride ASE with a static step recovered the high-molecular-weight PAHs with the next highest efficiency (approximately 55%) and had standard deviations less than 10% (longer extraction times [> 30 min] with the methylene chloride would increase the recoveries of these analytes.) A comparison of the results from this study with those of a previous study using lignite coal fly ash illustrates the difficulty in developing and adapting analyte-specific extraction methods for analytes that are adsorbed on different matrices.

  9. Accelerated solvent extraction for GC-based tobacco fingerprinting and its comparison with simultaneous distillation and extraction.

    Science.gov (United States)

    Li, Yong; Pang, Tao; Guo, Ziming; Li, Yanli; Wang, Xiaolin; Deng, Jianhua; Zhong, Kejun; Lu, Xin; Xu, Guowang

    2010-04-15

    An accelerated solvent extraction (ASE) procedure has been developed as a pretreatment method for chemical fingerprinting of volatile and semi-volatile components in cut tobacco. The ASE extraction conditions including temperature, operation pressure and extraction cycles were optimized to maximize extraction yield. The method was validated with repeatability, recovery and linearity. Compared with simultaneous distillation extraction (SDE), ASE provides higher extraction yields, less extraction time, lower solvent consumption and less labor time, and is more suitable for tobacco sample preparation. A typical ASE extract was analyzed by gas chromatography/time-of-flight mass spectrometry (GC-TOFMS). A total of 305 components with signal-to-noise ratio higher than 100 were tentatively identified by NIST05 and Wiley database. Finally, 36 cigarette samples from six cigarette brands were analyzed using the developed chemical fingerprinting method. Partial least squares-discriminant analysis shows good discrimination of different cigarette brands. The results indicate that ASE method can serve as high-throughput sample preparation technique for cigarette chemical fingerprint analysis.

  10. Response surface methodology to optimise Accelerated Solvent Extraction of steviol glycosides from Stevia rebaudiana Bertoni leaves.

    Science.gov (United States)

    Jentzer, Jean-Baptiste; Alignan, Marion; Vaca-Garcia, Carlos; Rigal, Luc; Vilarem, Gérard

    2015-01-01

    Following the approval of steviol glycosides as a food additive in Europe in December 2011, large-scale stevia cultivation will have to be developed within the EU. Thus there is a need to increase the efficiency of stevia evaluation through germplasm enhancement and agronomic improvement programs. To address the need for faster and reproducible sample throughput, conditions for automated extraction of dried stevia leaves using Accelerated Solvent Extraction were optimised. A response surface methodology was used to investigate the influence of three factors: extraction temperature, static time and cycle number on the stevioside and rebaudioside A extraction yields. The model showed that all the factors had an individual influence on the yield. Optimum extraction conditions were set at 100 °C, 4 min and 1 cycle, which yielded 91.8% ± 3.4% of total extractable steviol glycosides analysed. An additional optimisation was achieved by reducing the grind size of the leaves giving a final yield of 100.8% ± 3.3%.

  11. Compound Specific Extraction of Camptothecin from Nothapodytes nimmoniana and Piperine from Piper nigrum Using Accelerated Solvent Extractor.

    Science.gov (United States)

    Upadhya, Vinayak; Pai, Sandeep R; Sharma, Ajay K; Hegde, Harsha V; Kholkute, Sanjiva D; Joshi, Rajesh K

    2014-01-01

    Effects of varying temperatures with constant pressure of solvent on extraction efficiency of two chemically different alkaloids were studied. Camptothecin (CPT) from stem of Nothapodytes nimmoniana (Grah.) Mabb. and piperine from the fruits of Piper nigrum L. were extracted using Accelerated Solvent Extractor (ASE). Three cycles of extraction for a particular sample cell at a given temperature assured complete extraction. CPT and piperine were determined and quantified by using a simple and efficient UFLC-PDA (245 and 343 nm) method. Temperature increased efficiency of extraction to yield higher amount of CPT, whereas temperature had diminutive effect on yield of piperine. Maximum yield for CPT was achieved at 80°C and for piperine at 40°C. Thus, the study determines compound specific extraction of CPT from N. nimmoniana and piperine from P. nigrum using ASE method. The present study indicates the use of this method for simple, fast, and accurate extraction of the compound of interest.

  12. Application of accelerated solvent extraction in the analysis of organic contaminants, bioactive and nutritional compounds in food and feed.

    Science.gov (United States)

    Sun, Hanwen; Ge, Xusheng; Lv, Yunkai; Wang, Anbang

    2012-05-11

    Accelerated solvent extraction (ASE) has become a popular green extraction technology for different classes of organic contaminants present in numerous kinds of food and feed for food safety. The parameters affecting ASE efficiency and application advancement of ASE in the analysis of organic contaminants, natural toxins compounds as well as bioactive and nutritional compounds in animal origin food, plant origin food and animal feed are reviewed in detail. ASE is a fully automated and reliable extraction technique with many advantages over traditional extraction techniques, so it could be especially useful for routine analyses of pollutants in food and feed.

  13. Comparison of microwave, ultrasound and accelerated-assisted solvent extraction for recovery of polyphenols from Citrus sinensis peels.

    Science.gov (United States)

    Nayak, Balunkeswar; Dahmoune, Farid; Moussi, Kamal; Remini, Hocine; Dairi, Sofiane; Aoun, Omar; Khodir, Madani

    2015-11-15

    Peel of Citrus sinensis contains significant amounts of bioactive polyphenols that could be used as ingredients for a number of value-added products with health benefits. Extraction of polyphenols from the peels was performed using a microwave-assisted extraction (MAE) technique. The effects of aqueous acetone concentration, microwave power, extraction time and solvent-to-solid ratio on the total phenolic content (TPC), total antioxidant activity (TAA) (using DPPH and ORAC-values) and individual phenolic acids (IPA) were investigated using a response surface method. The TPC, TAA and IPA of peel extracts using MAE was compared with conventional, ultrasound-assisted and accelerated solvent extraction. The maximum predicted TPC under the optimal MAE conditions (51% acetone concentration in water (v/v), 500 W microwave power, 122 s extraction time and 25 mL g(-1) solvent to solid ratio), was 12.20 mg GAE g(-1) DW. The TPC and TAA in MAE extracts were higher than the other three extracts.

  14. Optimization of in-cell accelerated solvent extraction technique for the determination of organochlorine pesticides in river sediments.

    Science.gov (United States)

    Duodu, Godfred Odame; Goonetilleke, Ashantha; Ayoko, Godwin A

    2016-04-01

    Organochlorine pesticides (OCPs) are ubiquitous environmental contaminants with adverse impacts on aquatic biota, wildlife and human health even at low concentrations. However, conventional methods for their determination in river sediments are resource intensive. This paper presents an approach that is rapid and also reliable for the detection of OCPs. Accelerated Solvent Extraction (ASE) with in-cell silica gel clean-up followed by Triple Quadrupole Gas Chromatograph Mass Spectrometry (GCMS/MS) was used to recover OCPs from sediment samples. Variables such as temperature, solvent ratio, adsorbent mass and extraction cycle were evaluated and optimized for the extraction. With the exception of Aldrin, which was unaffected by any of the variables evaluated, the recovery of OCPs from sediment samples was largely influenced by solvent ratio and adsorbent mass and, to some extent, the number of cycles and temperature. The optimized conditions for OCPs extraction in sediment with good recoveries were determined to be 4 cycles, 4.5 g of silica gel, 105 °C, and 4:3 v/v DCM: hexane mixture. With the exception of two compounds (α-BHC and Aldrin) whose recoveries were low (59.73 and 47.66% respectively), the recovery of the other pesticides were in the range 85.35-117.97% with precision <10% RSD. The method developed significantly reduces sample preparation time, the amount of solvent used, matrix interference, and is highly sensitive and selective.

  15. Evaluating the performances of accelerated-solvent extraction, microwave-assisted extraction, and ultrasonic-assisted extraction for determining PCBs, HCHs and DDTs in sediments

    Institute of Scientific and Technical Information of China (English)

    ZHANG Peng; GE Linke; ZHOU Chuanguang; YAOZiwei

    2011-01-01

    Three extraction techniques have been recently used for the quantitative extraction of semi-volatile organic pollutants in sediments,i.e.accelerated solvent extraction (ASE),microwave assisted extraction (MAE) and ultrasonic assisted extraction (UAE).However,their extraction efficiencies have rarely been quantitatively compared using rigorous mathematical methods.In this paper,one-way analysis of variance (ANOVA) was employed to evaluate the performance of ASE,MAE and UAE in the overall extraction of PCBs,DDTs and HCHs by analysis of their recoveries from the Standard Reference Material IAEA-417,a sediment sample certified by many international laboratories.Conclusions were drawn at a significance level of P≤0.05.No significant differences were found among the mean values for method recoveries using ASE,MAE and UAE.The mean values for real recoveries using ASE and MAE were nearly identical,but the real recovery using UAE was much lower.The concentrations of all PCBs,DDTs and HCHs except for CB52 and o,p'-DDT using UAE were the lowest.Comparing the results obtained using ASE with MAE,the concentrations of CB28,CB52,CB138,α-HCH,β-HCH,p,p'-DDE and p,p'-DDD were nearly identical,while the concentrations of other compounds were significantly different.Based on the low recoveries,it was concluded that UAE is a relatively inefficient extraction method,while ASE and MAE are equivalent methods.Taking into consideration the relative standard deviation (RSD)values,solvent volume,extraction time,and purchasing costs of the apparatus,MAE was considered superior to ASE for extraction of PCBs,DDTs and HCHs.

  16. Compound Specific Extraction of Camptothecin from Nothapodytes nimmoniana and Piperine from Piper nigrum Using Accelerated Solvent Extractor

    Directory of Open Access Journals (Sweden)

    Vinayak Upadhya

    2014-01-01

    Full Text Available Effects of varying temperatures with constant pressure of solvent on extraction efficiency of two chemically different alkaloids were studied. Camptothecin (CPT from stem of Nothapodytes nimmoniana (Grah. Mabb. and piperine from the fruits of Piper nigrum L. were extracted using Accelerated Solvent Extractor (ASE. Three cycles of extraction for a particular sample cell at a given temperature assured complete extraction. CPT and piperine were determined and quantified by using a simple and efficient UFLC-PDA (245 and 343 nm method. Temperature increased efficiency of extraction to yield higher amount of CPT, whereas temperature had diminutive effect on yield of piperine. Maximum yield for CPT was achieved at 80∘C and for piperine at 40∘C. Thus, the study determines compound specific extraction of CPT from N. nimmoniana and piperine from P. nigrum using ASE method. The present study indicates the use of this method for simple, fast, and accurate extraction of the compound of interest.

  17. Influence of processing procedure on the quality of Radix Scrophulariae: a quantitative evaluation of the main compounds obtained by accelerated solvent extraction and high-performance liquid chromatography.

    Science.gov (United States)

    Cao, Gang; Wu, Xin; Li, Qinglin; Cai, Hao; Cai, Baochang; Zhu, Xuemei

    2015-02-01

    An improved high-performance liquid chromatography with diode array detection combined with accelerated solvent extraction method was used to simultaneously determine six compounds in crude and processed Radix Scrophulariae samples. Accelerated solvent extraction parameters such as extraction solvent, temperature, number of cycles, and analysis procedure were systematically optimized. The results indicated that compared with crude Radix Scrophulariae samples, the processed samples had lower contents of harpagide and harpagoside but higher contents of catalpol, acteoside, angoroside C, and cinnamic acid. The established method was sufficiently rapid and reliable for the global quality evaluation of crude and processed herbal medicines.

  18. Determination of persistent organic pollutants in solid environmental samples using accelerated solvent extraction and supercritical fluid extraction. Exhaustive extraction and sorption/desorption studies of PCBs

    Energy Technology Data Exchange (ETDEWEB)

    Bjoerklund, E.

    1998-10-01

    Human activity is constantly causing environmental problems due to production and release of numerous chemicals. A group of compounds of special concern is persistent organic pollutants (POP). These toxic, lipophilic chemicals have a high chemical and biological stability, and tend to accumulate in the lipid phase of living organisms. A major sink for POPs are sediments, and consequently these are important for the distribution of POPs in the aquatic environment. Traditionally, determination of POPs relay on exhaustive extraction using liquid extraction techniques (e.g. Soxhlet extraction developed in the late 19th century) followed by gas chromatographic analysis. Since liquid-solid extraction normally requires large volumes of organic solvents in combination with long extraction times and extract clean-up, there has been an increasing demand for improved technology. This should result in reduced organic solvent consumption and sample preparation time, at the same time improving the environment and cutting costs for POP monitoring. In this thesis two modern techniques with capability of fulfilling at least one of these goals have been investigated: (1) Supercritical Fluid Extraction (SFE), and (2) Accelerated Solvent Extraction (ASE). Polychlorinated biphenyls (PCBs) were chosen as model compounds in all experiments performed on environmental matrices, since they cover a relatively large range of physiochemical parameters. Important parameters influencing the overall extraction efficiency in ASE and SFE, are discussed and illustrated for a large number of sediments. It was demonstrated that, by careful consideration of the experimental parameters, both techniques are capable of replacing old methods such as Soxhlet extraction. ASE is somewhat faster than SFE, but the extracts generated in SFE are much cleaner and can be analyzed without sample clean-up. Consequently the overall sample preparation time may be substantially lower using SFE. However, ASE is important

  19. Influence of Accelerated Solvent Extraction and Ultrasound-Assisted Extraction on the Anthocyanin Profile of Different Vaccinium Species in the Context of Statistical Models for Authentication.

    Science.gov (United States)

    Heffels, Peter; Weber, Fabian; Schieber, Andreas

    2015-09-02

    Anthocyanins are frequently discussed as marker compounds for fruit product authenticity. Proper analysis including sample preparation for the determination of anthocyanin concentrations is crucial for the comparability of authenticity data. The present study determined the influence of accelerated solvent extraction (ASE) and ultrasound-assisted extraction (UAE), using two different solvent compositions on the anthocyanin profile of bilberries (Vaccinium myrtillus L.), lowbush blueberries (Vaccinium angustifolium Ait.), and American cranberries (Vaccinium macrocarpon Ait.). Besides differences in total anthocyanin concentrations in the extracts, significant deviations (p ≤ 0.05) in the individual anthocyanin concentration were observed, resulting in differing anthocyanin proportions. Linear discriminant analysis comparing the differences caused by the extraction method to the natural differences within a set of 26 bilberry and lowbush blueberry samples of different origins was conducted. It revealed that profile variations induced by the extraction methods are in a similar scale to profile variations as a result of geographic and climatic differences.

  20. Effect of the drying process on the intensification of phenolic compounds recovery from grape pomace using accelerated solvent extraction.

    Science.gov (United States)

    Rajha, Hiba N; Ziegler, Walter; Louka, Nicolas; Hobaika, Zeina; Vorobiev, Eugene; Boechzelt, Herbert G; Maroun, Richard G

    2014-01-01

    In light of their environmental and economic interests, food byproducts have been increasingly exploited and valorized for their richness in dietary fibers and antioxidants. Phenolic compounds are antioxidant bioactive molecules highly present in grape byproducts. Herein, the accelerated solvent extraction (ASE) of phenolic compounds from wet and dried grape pomace, at 45 °C, was conducted and the highest phenolic compounds yield (PCY) for wet (16.2 g GAE/100 g DM) and dry (7.28 g GAE/100 g DM) grape pomace extracts were obtained with 70% ethanol/water solvent at 140 °C. The PCY obtained from wet pomace was up to two times better compared to the dry byproduct and up to 15 times better compared to the same food matrices treated with conventional methods. With regard to Resveratrol, the corresponding dry pomace extract had a better free radical scavenging activity (49.12%) than the wet extract (39.8%). The drying pretreatment process seems to ameliorate the antiradical activity, especially when the extraction by ASE is performed at temperatures above 100 °C. HPLC-DAD analysis showed that the diversity of the flavonoid and the non-flavonoid compounds found in the extracts was seriously affected by the extraction temperature and the pretreatment of the raw material. This diversity seems to play a key role in the scavenging activity demonstrated by the extracts. Our results emphasize on ASE usage as a promising method for the preparation of highly concentrated and bioactive phenolic extracts that could be used in several industrial applications.

  1. Effect of the Drying Process on the Intensification of Phenolic Compounds Recovery from Grape Pomace Using Accelerated Solvent Extraction

    Directory of Open Access Journals (Sweden)

    Hiba N. Rajha

    2014-10-01

    Full Text Available In light of their environmental and economic interests, food byproducts have been increasingly exploited and valorized for their richness in dietary fibers and antioxidants. Phenolic compounds are antioxidant bioactive molecules highly present in grape byproducts. Herein, the accelerated solvent extraction (ASE of phenolic compounds from wet and dried grape pomace, at 45 °C, was conducted and the highest phenolic compounds yield (PCY for wet (16.2 g GAE/100 g DM and dry (7.28 g GAE/100 g DM grape pomace extracts were obtained with 70% ethanol/water solvent at 140 °C. The PCY obtained from wet pomace was up to two times better compared to the dry byproduct and up to 15 times better compared to the same food matrices treated with conventional methods. With regard to Resveratrol, the corresponding dry pomace extract had a better free radical scavenging activity (49.12% than the wet extract (39.8%. The drying pretreatment process seems to ameliorate the antiradical activity, especially when the extraction by ASE is performed at temperatures above 100 °C. HPLC-DAD analysis showed that the diversity of the flavonoid and the non-flavonoid compounds found in the extracts was seriously affected by the extraction temperature and the pretreatment of the raw material. This diversity seems to play a key role in the scavenging activity demonstrated by the extracts. Our results emphasize on ASE usage as a promising method for the preparation of highly concentrated and bioactive phenolic extracts that could be used in several industrial applications.

  2. Accelerated solvent extraction combined with solid phase extraction for the determination of organophosphate esters from sewage sludge compost by UHPLC-MS/MS.

    Science.gov (United States)

    Pang, Long; Yang, Peijie; Ge, Liming; Du, Jingjing; Zhang, Hongzhong

    2017-02-01

    Organophosphate esters (OPEs), widely used as flame retardants and plasticizers, are regarded as emerging pollutants. OPEs are prone to concentrate into residual activated sludge, which might cause secondary pollution if not suitably treated. Composting is an economical and effective approach to make sewage sludge stable and harmless. Therefore, it is essential to develop a novel method for analyzing OPEs in sewage sludge compost samples. However, in the composting process, large amounts of amendments are doped into the sludge to adjust the carbon-nitrogen ratio. Amendment has a strong capacity for adsorption and thus induces a decrease of extraction efficiency. This study developed a novel procedure for determining OPEs in compost samples. Accelerated solvent extraction (ASE) and solid phase extraction (SPE) were used for extracting and concentrating the OPEs from sewage sludge compost samples, and then analyzed by UHPLC-MS/MS. Some parameters were optimized in this study, mainly including the extraction solvent type, extraction temperature, static extraction time, extraction cycles, and flush volume. Under the optimal conditions, the proposed method showed good linearity between 0.50 and 100 μg kg(-1) with regression coefficients in the range of 0.9984-0.9998. Detection limits were in the range of 0.02-3 μg kg(-1) with standard deviations ranging from 2 to 6%. Acceptable recoveries between 56 and 119% for samples spiked at different concentration levels were achieved. In contrast, the recoveries merely ranged from 24 to 58% by using ultrasonic-assisted extraction. Graphical abstract A comparison of recoveries between ultrasonic-assisted extraction (UAS) and accelerated solvent extraction (ASE) for organophosphate esters from sewage sludge compost samples.

  3. Supercritical solvent coal extraction

    Science.gov (United States)

    Compton, L. E. (Inventor)

    1984-01-01

    Yields of soluble organic extract are increased up to about 50% by the supercritical extraction of particulate coal at a temperature below the polymerization temperature for coal extract fragments (450 C.) and a pressure from 500 psig to 5,000 psig by the conjoint use of a solvent mixture containing a low volatility, high critical temperature coal dissolution catalyst such as phenanthrene and a high volatility, low critical temperature solvent such as toluene.

  4. The Rate of Success of the Accelerated Solvent Extraction (Ase of Fat and Organochlorine Pesticides from Dried Fish Meat Samples

    Directory of Open Access Journals (Sweden)

    Ana Andreea CIOCA

    2017-05-01

    Full Text Available The replacement of conventional sample preparation techniques with newer techniques which are automated, faster and more eco-friendly, is nowadays desired in every analytical laboratory. One of the techniques with the attributes mentioned above is the Accelerated Solvent Extraction. In order to evaluate how successful this method is for the extraction of fat and organochlorine pesticides (OCPs from dried fish meat samples, we have tested two series of diverse fish using Dionex™ 350 ASE provided by Thermo Scientific™ (Germany. For a more interesting approach, we added to our investigation 7 polychlorinated biphenyl (PCBs, 3 thricholorobenzenes, 2 tetrachlorobenzenes, 1 pentachlorobenzenes and 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD. The study focused on comparing the recoveries of these analytes from different fish samples, after replacing the conventional reference method of the laboratory with ASE. The ASE parameters tested were previously used for the extraction of fat and polybrominated diphenyl ethers (PBDE from fish samples: temperature: 120 ° C; static time: 5 min; number of cycles: 3; flushing volume: 25%; rinse with nitrogen: 90 s; solvent: cyclohexane/ethyl acetate (ratio 1:1. The ASE method provided similar and in some cases better results when compared to the standard reference method, more rapidly, eco-friendly and safer. Any high or low recoveries of the analytes taken into study are attributed to random or systematic errors during the Clean-up step of the extracts and the quantification with Gas Chromatography coupled with Tandem Mass-Spectrometry (GC MS/MS.

  5. Accelerated solvent extraction followed by on-line solid-phase extraction coupled to ion trap LC/MS/MS for analysis of benzalkonium chlorides in sediment samples

    Science.gov (United States)

    Ferrer, I.; Furlong, E.T.

    2002-01-01

    Benzalkonium chlorides (BACs) were successfully extracted from sediment samples using a new methodology based on accelerated solvent extraction (ASE) followed by an on-line cleanup step. The BACs were detected by liquid chromatography/ion trap mass spectrometry (LC/MS) or tandem mass spectrometry (MS/MS) using an electrospray interface operated in the positive ion mode. This methodology combines the high efficiency of extraction provided by a pressurized fluid and the high sensitivity offered by the ion trap MS/MS. The effects of solvent type and ASE operational variables, such as temperature and pressure, were evaluated. After optimization, a mixture of acetonitrile/water (6:4 or 7:3) was found to be most efficient for extracting BACs from the sediment samples. Extraction recoveries ranged from 95 to 105% for C12 and C14 homologues, respectively. Total method recoveries from fortified sediment samples, using a cleanup step followed by ASE, were 85% for C12BAC and 79% for C14-BAC. The methodology developed in this work provides detection limits in the subnanogram per gram range. Concentrations of BAC homologues ranged from 22 to 206 ??g/kg in sediment samples from different river sites downstream from wastewater treatment plants. The high affinity of BACs for soil suggests that BACs preferentially concentrate in sediment rather than in water.

  6. Accelerated solvent extraction combined with dispersive liquid-liquid microextraction before gas chromatography with mass spectrometry for the sensitive determination of phenols in soil samples.

    Science.gov (United States)

    Xing, Han-Zhu; Wang, Xia; Chen, Xiang-Feng; Wang, Ming-Lin; Zhao, Ru-Song

    2015-05-01

    A method combining accelerated solvent extraction with dispersive liquid-liquid microextraction was developed for the first time as a sample pretreatment for the rapid analysis of phenols (including phenol, m-cresol, 2,4-dichlorophenol, and 2,4,6-trichlorophenol) in soil samples. In the accelerated solvent extraction procedure, water was used as an extraction solvent, and phenols were extracted from soil samples into water. The dispersive liquid-liquid microextraction technique was then performed on the obtained aqueous solution. Important accelerated solvent extraction and dispersive liquid-liquid microextraction parameters were investigated and optimized. Under optimized conditions, the new method provided wide linearity (6.1-3080 ng/g), low limits of detection (0.06-1.83 ng/g), and excellent reproducibility (extraction with dispersive liquid-liquid microextraction as a sample pretreatment procedure coupled with gas chromatography and mass spectrometry is an excellent method for the rapid analysis of trace levels of phenols in environmental soil samples.

  7. Semiautomatic sequential extraction of polycyclic aromatic hydrocarbons and elemental bio-accessible fraction by accelerated solvent extraction on a single particulate matter sample.

    Science.gov (United States)

    Astolfi, Maria Luisa; Di Filippo, Patrizia; Gentili, Alessandra; Canepari, Silvia

    2017-11-01

    We describe the optimization and validation of a sequential extractive method for the determination of the polycyclic aromatic hydrocarbons (PAHs) and elements (Al, As, Cd, Cr, Cu, Fe, Mn, Ni, Pb, Se, V and Zn) that are chemically fractionated into bio-accessible and mineralized residual fractions on a single particulate matter filter. The extraction is performed by automatic accelerated solvent extraction (ASE); samples are sequentially treated with dichloromethane/acetone (4:1) for PAHs extraction and acetate buffer (0.01M; pH 4.5) for elements extraction (bio-accessible fraction). The remaining solid sample is then collected and subjected to acid digestion with HNO3:H2O2 (2:1) to determine the mineralized residual element fraction. We also describe a homemade ASE cell that reduces the blank values for most elements; in this cell, the steel frit was replaced by a Teflon pierced disk and a Teflon cylinder was used as the filler. The performance of the proposed method was evaluated in terms of recovery from standard reference material (SRM 1648 and SRM 1649a) and repeatability. The equivalence between the new ASE method and conventional methods was verified for PAHs and for bio-accessible and mineralized residual fractions of elements on PM10 twin filters. Copyright © 2017 Elsevier B.V. All rights reserved.

  8. Accelerated solvent extraction method for the quantification of polycyclic aromatic hydrocarbons in cocoa beans by gas chromatography-mass spectrometry.

    Science.gov (United States)

    Belo, Renata França Cassimiro; Figueiredo, Júlia Pereira; Nunes, Carolina Mariana; Pissinatti, Rafael; Souza, Scheilla Vitorino Carvalho de; Junqueira, Roberto Gonçalves

    2017-05-15

    An accelerated solvent extraction (ASE) procedure for use with gas chromatography-mass spectrometry (GC-MS) was optimized for the determination of eight polycyclic aromatic hydrocarbons (PAHs) in cocoa beans. Plackett-Burman and rotatable central composite design (RCCD) indicated that three variables affected the recoveries of PAHs during the extraction and purification steps: agitation time in the second liquid-liquid partition, weight of silica gel in the column, and volume of hexane for PAH elution from the column. After obtaining the optimal conditions, a single laboratory method validation was performed. Linearity was demonstrated for benzo[a]pyrene in the concentration range from 0.5 to 8.0mgkg(-1) of sample, corresponding to 1.25-20.0μgkg(-1) of cocoa on a fat basis. For the other analytes, linearity was observed from 0.75 to 8.0μgkg(-1) of sample (1.88-20.0μgkg(-1) of cocoa on a fat basis). Significant matrix effects were found for chrysene and benzo[b]fluoranthene. The precision of the method was verified with relative standard deviations (RSDs) ranging from 2.57 to 14.13% and from 4.36 to 19.77% under repeatability and intermediate precision conditions, respectively. The average recoveries of the eight PAHs ranged from 74.99 to 109.73%. These parameters, limits and measurement uncertainties met the performance criteria established by European Union regulations, except for the theoretical limit of detection for chrysene. The method was applied to the analysis of samples of Brazilian cocoa beans, and only one sample was found to have a PAH content above the maximum limit defined by the European Union legislation. This optimized and validated method is intended to be used as part of the official Brazilian monitoring programs investigating contaminants and residues in food. Copyright © 2017 Elsevier B.V. All rights reserved.

  9. High-throughput GC-ECD analysis of PCBs in food by accelerated solvent extraction. Method validation

    Energy Technology Data Exchange (ETDEWEB)

    Piersanti, A.; Fioroni, L.; Paoloni, A.; Tavoloni, T.; Pecorelli, I.; Galarini, R. [Istituto Zooprofilattico Sperimentale dell' Umbria e delle Marche, Perugia (Italy)

    2004-09-15

    In the year 2000 the determination of the PCBs in food commodities was introduced in the Italian national residue control plan in which government labs were requested to estimate the total PCB content as sum of seven more representative congeners. Later on, in 2001, it was decided that a more appropriate estimation of the total PCBs was possible through analysis of eighteen rather than seven congeners. Therefore the need for simple and validated analytical methods arose. In this work a method for the analysis of the PCBs 18-congeners (T{sub 3}CB-28, T{sub 4}CB-52, P{sub 5}CB-95, P{sub 5}CB-99, P{sub 5}CB-101, P{sub 5}CB-105, P{sub 5}CB-110, P{sub 5}CB-118, H{sub 6}CB-138, H{sub 6}CB-146, H{sub 6}CB-149, H{sub 6}CB-151, H{sub 6}CB-153, H{sub 7}CB-170, H{sub 7}CB-177, H{sub 7}CB-180, H{sub 7}CB-183, H{sub 7}CB-187) is reported. This has been set up taking in account the advantages of the automated and high efficient Accelerated Solvent Extraction together with good purification achieved by a one-step acidic-extrelut/silica chromatography. The instrumental analysis is performed by capillary-GC equipped with an ECD detector. An in-house validation study has been made on swine muscle assessing the method performances in terms of limit of detection, response linearity range, trueness and precision.

  10. Occupational exposure to complex mixtures of volatile organic compounds in ambient air: desorption from activated charcoal using accelerated solvent extraction can replace carbon disulfide?

    Science.gov (United States)

    Fabrizi, Giovanni; Fioretti, Marzia; Rocca, Lucia Mainero

    2013-01-01

    A desorption study of 57 volatile organic compounds (VOCs) has been conducted by use of accelerated solvent extraction (ASE) and gas chromatography-mass spectrometry. Different solvents were tested to extract activated charcoal tubes with the objective of replacing carbon disulfide, used in official methods, because of its highly toxic health and environmental effects. Extraction conditions, for example temperature and number of cycles, were investigated and optimized. The definitive extraction procedure selected was use of acetone at 150 °C and two consecutive extraction cycles at a pressure of 1,500 psi. Considering a sample volume of 0.005 Nm(3), corresponding to a sampling time of 8 h at a flow rate of 0.01 L min(-1), the method was validated over the concentration range 65-26,300 μg Nm(-3). The lowest limit of quantification was 6 μg Nm(-3), and recovery for the 93 % of analytes ranged from 65 to 102 %. For most of the compounds, relative standard deviations were less than 15 % for inter and intra-day precision. Uncertainty of measurement was also determined: the relative expanded uncertainty was always below 29.6 %, except for dichlorodifluoromethane. This work shows that use of friendlier solvent, for example acetone, coupled with use of ASE, can replace use of CS(2) for chemical removal of VOCs from activated charcoal. ASE has several advantages over traditional solvent-extraction methods, including shorter extraction time, minimum sample manipulation, high reproducibility, and less extraction discrimination. No loss of sensitivity occurs and there is also a salutary effect on bench workers' health and on the smell of laboratory air.

  11. SOLVENT EXTRACTION OF URANIUM VALUES

    Science.gov (United States)

    Feder, H.M.; Ader, M.; Ross, L.E.

    1959-02-01

    A process is presented for extracting uranium salt from aqueous acidic solutions by organic solvent extraction. It consists in contacting the uranium bearing solution with a water immiscible dialkylacetamide having at least 8 carbon atoms in the molecule. Mentioned as a preferred extractant is dibutylacetamide. The organic solvent is usually used with a diluent such as kerosene or CCl/sub 4/.

  12. Development, comparison and application of sorbent-assisted accelerated solvent extraction, microwave-assisted extraction and ultrasonic-assisted extraction for the determination of polybrominated diphenyl ethers in sediments.

    Science.gov (United States)

    Song, Shanjun; Shao, Mingwu; Tang, Hua; He, Yajuan; Wang, Weihua; Liu, Liliang; Wu, Jiajia

    2016-12-02

    Fast and selective analytical methods were developed based on sorbent-assisted mechanism and microwave-assisted extraction (SA-MAE), accelerate solvent extraction (SA-ASE) and ultrasonic-assisted extraction (SA-UAE) for the determination of polybrominated diphenyl ethers (PBDEs) in sediments. The experimental parameters, such as extraction conditions and sorbent amounts, were optimized according to Taguchi Orthogonal Arrays. The accuracy of developed SA-methods was a satisfactory ranging from 71% to 118%. The inter/intra-day RSDs were extraction intensity may produce various matrix effects. In addition, the developed SA-ASE method was successfully applied on real environmental samples collected from a typical polluted area. The data and calculation suggested local environmental contamination pattern and potential pollution source.

  13. Determination of polychlorinated biphenyls in fish: optimisation and validation of a method based on accelerated solvent extraction and gas chromatography-mass spectrometry.

    Science.gov (United States)

    Ottonello, Giuliana; Ferrari, Angelo; Magi, Emanuele

    2014-01-01

    A simple and robust method for the determination of 18 polychlorinated biphenyls (PCBs) in fish was developed and validated. A mixture of acetone/n-hexane (1:1, v/v) was selected for accelerated solvent extraction (ASE). After the digestion of fat, the clean-up was carried out using solid phase extraction silica cartridges. Samples were analysed by GC-MS in selected ion monitoring (SIM) using three fragment ions for each congener (one quantifier and two qualifiers). PCB 155 and PCB 198 were employed as internal standards. The lowest limit of detection was observed for PCB 28 (0.4ng/g lipid weight). The accuracy of the method was verified by means of the Certified Reference Material EDF-2525 and good results in terms of linearity (R(2)>0.994) and recoveries (80-110%) were also achieved. Precision was evaluated by spiking blank samples at 4, 8 and 12ng/g. Relative standard deviation values for repeatability and reproducibility were lower than 8% and 16%, respectively. The method was applied to the determination of PCBs in 80 samples belonging to four Mediterranean fish species. The proposed procedure is particularly effective because it provides good recoveries with lowered extraction time and solvent consumption; in fact, the total time of extraction is about 12min per sample and, for the clean-up step, a total solvent volume of 13ml is required. Copyright © 2013 Elsevier Ltd. All rights reserved.

  14. Optimization of an accelerated solvent extraction dispersive liquid-liquid microextraction method for the separation and determination of essential oil from Ligusticum chuanxiong Hort by gas chromatography with mass spectrometry.

    Science.gov (United States)

    Yang, Guang; Sun, Qiushi; Hu, Zhiyan; Liu, Hua; Zhou, Tingting; Fan, Guorong

    2015-10-01

    In this study, an accelerated solvent extraction dispersive liquid-liquid microextraction coupled with gas chromatography and mass spectrometry was established and employed for the extraction, concentration and analysis of essential oil constituents from Ligusticum chuanxiong Hort. Response surface methodology was performed to optimize the key parameters in accelerated solvent extraction on the extraction efficiency, and key parameters in dispersive liquid-liquid microextraction were discussed as well. Two representative constituents in Ligusticum chuanxiong Hort, (Z)-ligustilide and n-butylphthalide, were quantitatively analyzed. It was shown that the qualitative result of the accelerated solvent extraction dispersive liquid-liquid microextraction approach was in good agreement with that of hydro-distillation, whereas the proposed approach took far less extraction time (30 min), consumed less plant material (usually extraction and analysis of essential oil.

  15. Development and validation of an automated extraction method (accelerated solvent extraction) and a reverse-phase HPLC analysis method for assay of ivermectin in a meat-based chewable formulation.

    Science.gov (United States)

    Abend, Andreas M; Chung, Le; McCollum, David G; Wuelfing, W Peter

    2003-04-10

    A new method for monitoring ivermectin content in HEARTGARD CHEWABLES has been developed and validated. The method consists of the automated extraction of ivermectin from the meat-based formulation under conditions of elevated temperature and pressure (accelerated solvent extraction, ASE, and determination of the active by reverse-phase high performance liquid chromatography (HPLC). The method resolves both active species of ivermectin (components H(2)B(1a) and H(2)B(1b)) from the formulation matrix.

  16. Accelerated solvent extraction and analysis of tea polyphenols%茶多酚的加速溶剂萃取与分析

    Institute of Scientific and Technical Information of China (English)

    赵敏; 唐美华; 张之翼; 吕凤兰; 陈国松

    2012-01-01

    以毛尖茶叶为原料,用加速溶剂萃取法提取茶多酚粗品.用单因素试验研究和正交试验考察乙醇体积分数、温度和循环次数对萃取率的影响.用二极管阵列-高效液相色谱( DAD - HPLC)对照测定加速溶剂萃取的萘多酚粗品、微波辅助提取的萘多酚粗品和商品荼多酚.结果表明:茶多酚粗品的制备最佳条件为萃取温度160℃、乙醇体积分数60%、循环萃取2次.高温加速溶剂萃取法对茶多酚的粗提率较高,但其中儿茶素的总量却显著下降.降低提取温度,则茶多酚中的主要功能成分儿茶素的含量显著高于微波辅助提取法.%The gross tea polyphenols were extracted from Maojian tea by the accelerated solvent method. Single factor test and orthogonal design were used to explore the effects of ethanol volume fraction, temperature and cycle times on the extraction ratio. The comparison of gross polyphenols got from accelerated solvent extraction, microwave-assisted extraction and commodity was made by diode array detector-high performance liquid chromatography (DAD-HPLC) analysis. Results showed that the optimum operation conditions for gross polyphenlos extraction are 160 ℃ , 2 times, and 60% ethanol. The accelerated solvent extraction ratio at a high temperature was higher for the gross tea polyphenols and lower for the cate-chin. If the extraction temperature was dropped down to 40℃, the content of catechin was much higher than that from microwave-assisted extraction.

  17. Supercritical multicomponent solvent coal extraction

    Science.gov (United States)

    Corcoran, W. H.; Fong, W. S.; Pichaichanarong, P.; Chan, P. C. F.; Lawson, D. D. (Inventor)

    1983-01-01

    The yield of organic extract from the supercritical extraction of coal with larger diameter organic solvents such as toluene is increased by use of a minor amount of from 0.1 to 10% by weight of a second solvent such as methanol having a molecular diameter significantly smaller than the average pore diameter of the coal.

  18. Determination of organotin compounds in biological samples using accelerated solvent extraction, sodium tetraethylborate ethylation, and multicapillary gas chromatography-flame photometric detection.

    Science.gov (United States)

    Wasik, Andrzej; Ciesielski, Tomasz

    2004-03-01

    A method has been developed for species-selective analysis of organotin compounds in solid, biological samples. The procedure is based on accelerated solvent extraction (ASE) of analytes and includes extraction of the tin species with a methanol-water (90% methanol) solution of acetic acid/sodium acetate containing tropolone (0.03% w/ v), their ethylation with NaBEt(4), and separation and detection by GC-FPD. The analytical procedure was optimized with an unspiked sample of harbor porpoise ( Phocoena phocoena) liver. Effects of ASE operational variables (extraction temperature and pressure, solvent composition, number of static extraction steps) are discussed. Method detection limits (MDL) were in the range 6-10 ng(Sn) g(-1) dry weight and 7-17 ng(Sn) g(-1) dry weight for butyl- and phenyltin compounds, respectively. Recoveries were comparable with or better than those obtained by use of other procedures reported in the literature. The analytical procedure was validated by analysis of NIES No. 11 (fish tissue) certified reference material.

  19. Evaluating and modeling the effects of surface sampling factors on the recovery of organic chemical attribution signatures using the accelerated diffusion sampler and solvent extraction

    Energy Technology Data Exchange (ETDEWEB)

    Mo, Kai-For; Heredia-Langner, Alejandro; Fraga, Carlos G.

    2017-03-01

    In this study, an experimental design matrix was created and executed in order to test the effects of various real-world factors on the ability of the (1) accelerated diffusion sampler with solid phase micro-extraction (ADS-SPME) and (2) solvent extraction to capture organic chemical attribution signatures (CAS) from dimethyl methylphosphonate (DMMP) spiked onto painted wall board (PWB) surfaces. The DMMP CAS organic impurities sampled by ADS-SPME and solvent extraction were analyzed by gas chromatography/mass spectrometry (GC/MS). The number of detected DMMP CAS impurities and their respective GC/MS peak areas were determined as a function of DMMP stock, DMMP spiked volume, exposure time, SPME sampling time, and ADS headspace pressure. Based on the statistical analysis of experimental results, several general conclusions are made: (1) ADS-SPME with vacuum (i.e., reduced pressure) increased the amount of detected CAS impurity, as measured by GC/MS peak area, by a factor of 1.7 to 1.9 for PWB under certain experimental conditions, (2) the amount of detected CAS impurity was most influenced by spiked volume, stock, and ADS headspace pressure, (3) the ADS had no measurable effect on the number of detected DMMP impurities, that is, the ADS (with and without reduced pressure) had no practical effect on the DMMP impurity profile collected from spiked PWB, and (4) solvent extraction out performed ADS-SPME in terms of consistently capturing all or most of the targeted DMMP impurities from spiked PWB.

  20. Evaluating and modeling the effects of surface sampling factors on the recovery of organic chemical attribution signatures using the accelerated diffusion sampler and solvent extraction.

    Science.gov (United States)

    Mo, Kai-For; Heredia-Langner, Alejandro; Fraga, Carlos G

    2017-03-01

    In this study, an experimental design matrix was created and executed to test the effects of various real-world factors on the ability of (1) the accelerated diffusion sampler with solid phase micro-extraction (ADS-SPME) and (2) solvent extraction to capture organic chemical attribution signatures (CAS) from dimethyl methylphosphonate (DMMP) spiked onto painted wall board (PWB) surfaces. The DMMP CAS organic impurities sampled by ADS-SPME and solvent extraction were analyzed by gas chromatography/mass spectrometry (GC/MS). The number of detected DMMP CAS impurities and their respective GC/MS peak areas were determined as a function of DMMP stock, DMMP spiked volume, exposure time, SPME sampling time, and ADS headspace pressure. Based on the statistical analysis of experimental results, several general conclusions are made: (1) the amount of CAS impurity detected using ADS-SPME and GC/MS was most influenced by spiked volume, stock, and ADS headspace pressure, (2) reduced ADS headspace pressure increased the amount of detected CAS impurity, as measured by GC/MS peak area, by up to a factor of 1.7-1.9 compared to ADS at ambient headspace pressure, (3) the ADS had no measurable effect on the number of detected DMMP impurities, that is, ADS (with and without reduced pressure) had no practical effect on the DMMP impurity profile collected from spiked PWB, and (4) solvent extraction out performed ADS-SPME in terms of consistently capturing all or most of the targeted DMMP impurities from spiked PWB.

  1. Accelerated solvent extraction -gas chromatography to the residue of pesticides measurement%加速溶剂萃取-气相色谱法对土壤中农药残留的测定

    Institute of Scientific and Technical Information of China (English)

    孙志伟

    2015-01-01

    文章论述了加速溶剂萃取-气相色谱法对土壤中农药残留的测定方法.%This paper introduced the accelerated solvent extraction -gas chromatography to the residue of pesticides measurement.

  2. Validation and application of a multi-residue method, using accelerated solvent extraction followed by gas chromatography, for pesticides quantification in soil.

    Science.gov (United States)

    Leyva-Morales, J B; Valdez-Torres, J B; Bastidas-Bastidas, P J; Betancourt-Lozano, M

    2015-01-01

    A multi-residue method was developed to determine different types of pesticides in soils. An extraction with pressure and temperature, through accelerated solvent extraction (dichloromethane:acetone, 50:50, v/v). The pesticides were determined by gas chromatography with several selective detectors: electron capture detector, pulsed flame photometric detector and thermionic specific detector. The following parameters were determined: limit of detection, limit of quantification, equipment linearity (working interval), method linearity as well as, method accuracy and precision. The average recoveries ranged between 76 and 106%, with the exception of chlorothalonil, which had an average recovery of 46%. Additionally, detection limits from 0.9 to 7.6ng g -: (1) and the quantification limits from 3.00 to 25.47ng g -: (1) were estimated. In terms of linearity and precision, the results obtained were in the ranges considered adequate (R(2) ≥ 0.98 and coefficient of variation (CV) ≤ 20%), with the exception of aldrin (R(2) = 0.946, CV = 35.79%), lindane (R(2) = 0.917, CV = 32.91%) and chlorothalonil (R(2) = 0.8184, CV = 81.35%). The proposed method was used to evaluate pesticides in real soil samples, detecting concentrations over 1000ng g -: (1) for some pesticides. The method was correctly validated and provided for the rapid determination of pesticides in soil.

  3. Determination of Polymer Additives-Antioxidants, Ultraviolet Stabilizers, Plasticizers and Photoinitiators in Plastic Food Package by Accelerated Solvent Extraction Coupled with High-Performance Liquid Chromatography.

    Science.gov (United States)

    Li, Bo; Wang, Zhi-Wei; Lin, Qin-Bao; Hu, Chang-Ying; Su, Qi-Zhi; Wu, Yu-Mei

    2015-07-01

    An analytical method for the quantitative determination of 4 antioxidants, 9 ultraviolet (UV) stabilizers, 12 phthalate plasticizers and 2 photoinitiators in plastic food package using accelerated solvent extraction (ASE) coupled with high-performance liquid chromatography-photodiode array detector (HPLC-PDA) has been developed. Parameters affecting the efficiency in the process such as extraction and chromatographic conditions were studied in order to determine operating conditions. The analytical method of ASE-HPLC showed good linearity with good correlation coefficients (R ≥ 0.9833). The limits of detection and quantification were between 0.03 and 0.30 µg mL(-1) and between 0.10 and 1.00 µg mL(-1) for 27 analytes. Average spiked recoveries for most analytes in samples were >70.4% at 10, 20 and 40 µg g(-1) spiked levels, except UV-9 and Irganox 1010 (58.6 and 64.0% spiked at 10 µg g(-1), respectively), the relative standard deviations were in the range from 0.4 to 15.4%. The methodology has been proposed for the analysis of 27 polymer additives in plastic food package. © The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

  4. Evaluation of micro-colorimetric lipid determination method with samples prepared using sonication and accelerated solvent extraction methods

    Science.gov (United States)

    Two common laboratory extraction techniques were evaluated for routine use with the micro-colorimetric lipid determination method developed by Van Handel (1985) [E. Van Handel, J. Am. Mosq. Control Assoc. 1(1985) 302] and recently validated for small samples by Inouye and Lotufo ...

  5. Advanced integrated solvent extraction systems

    Energy Technology Data Exchange (ETDEWEB)

    Horwitz, E.P.; Dietz, M.L.; Leonard, R.A. [Argonne National Lab., IL (United States)

    1997-10-01

    Advanced integrated solvent extraction systems are a series of novel solvent extraction (SX) processes that will remove and recover all of the major radioisotopes from acidic-dissolved sludge or other acidic high-level wastes. The major focus of this effort during the last 2 years has been the development of a combined cesium-strontium extraction/recovery process, the Combined CSEX-SREX Process. The Combined CSEX-SREX Process relies on a mixture of a strontium-selective macrocyclic polyether and a novel cesium-selective extractant based on dibenzo 18-crown-6. The process offers several potential advantages over possible alternatives in a chemical processing scheme for high-level waste treatment. First, if the process is applied as the first step in chemical pretreatment, the radiation level for all subsequent processing steps (e.g., transuranic extraction/recovery, or TRUEX) will be significantly reduced. Thus, less costly shielding would be required. The second advantage of the Combined CSEX-SREX Process is that the recovered Cs-Sr fraction is non-transuranic, and therefore will decay to low-level waste after only a few hundred years. Finally, combining individual processes into a single process will reduce the amount of equipment required to pretreat the waste and therefore reduce the size and cost of the waste processing facility. In an ongoing collaboration with Lockheed Martin Idaho Technology Company (LMITCO), the authors have successfully tested various segments of the Advanced Integrated Solvent Extraction Systems. Eichrom Industries, Inc. (Darien, IL) synthesizes and markets the Sr extractant and can supply the Cs extractant on a limited basis. Plans are under way to perform a test of the Combined CSEX-SREX Process with real waste at LMITCO in the near future.

  6. Analysis of intracellular and extracellular microcystin variants in sediments and pore waters by accelerated solvent extraction and high performance liquid chromatography-tandem mass spectrometry.

    Science.gov (United States)

    Zastepa, Arthur; Pick, Frances R; Blais, Jules M; Saleem, Ammar

    2015-05-04

    The fate and persistence of microcystin cyanotoxins in aquatic ecosystems remains poorly understood in part due to the lack of analytical methods for microcystins in sediments. Existing methods have been limited to the extraction of a few extracellular microcystins of similar chemistry. We developed a single analytical method, consisting of accelerated solvent extraction, hydrophilic-lipophilic balance solid phase extraction, and reversed phase high performance liquid chromatography-tandem mass spectrometry, suitable for the extraction and quantitation of both intracellular and extracellular cyanotoxins in sediments as well as pore waters. Recoveries of nine microcystins, representing the chemical diversity of microcystins, and nodularin (a marine analogue) ranged between 75 and 98% with one, microcystin-RR (MC-RR), at 50%. Chromatographic separation of these analytes was achieved within 7.5 min and the method detection limits were between 1.1 and 2.5 ng g(-1) dry weight (dw). The robustness of the method was demonstrated on sediment cores collected from seven Canadian lakes of diverse geography and trophic states. Individual microcystin variants reached a maximum concentration of 829 ng g(-1) dw on sediment particles and 132 ng mL(-1) in pore waters and could be detected in sediments as deep as 41 cm (>100 years in age). MC-LR, -RR, and -LA were more often detected while MC-YR, -LY, -LF, and -LW were less common. The analytical method enabled us to estimate sediment-pore water distribution coefficients (K(d)), MC-RR had the highest affinity for sediment particles (log K(d)=1.3) while MC-LA had the lowest affinity (log K(d)=-0.4), partitioning mainly into pore waters. Our findings confirm that sediments serve as a reservoir for microcystins but suggest that some variants may diffuse into overlying water thereby constituting a new route of exposure following the dissipation of toxic blooms. The method is well suited to determine the fate and persistence of different

  7. Analysis of intracellular and extracellular microcystin variants in sediments and pore waters by accelerated solvent extraction and high performance liquid chromatography-tandem mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Zastepa, Arthur, E-mail: arthur.zastepa@gmail.com; Pick, Frances R.; Blais, Jules M.; Saleem, Ammar

    2015-05-04

    Highlights: • First analytical method for intracellular microcystins (MCs) in sediment. • Includes a suite of variants (LR, {sup 7dm}LR, RR, YR, WR, LA, LF, LY, LW) and nodularin. • Reports the first measurements of MCs in sediment pore waters. • MCs detected in >100 year old lake sediments suggesting long-term preservation. • Sediment-pore water distribution (K{sub d}) differed between variants suggesting differences in environmental fate. - Abstract: The fate and persistence of microcystin cyanotoxins in aquatic ecosystems remains poorly understood in part due to the lack of analytical methods for microcystins in sediments. Existing methods have been limited to the extraction of a few extracellular microcystins of similar chemistry. We developed a single analytical method, consisting of accelerated solvent extraction, hydrophilic–lipophilic balance solid phase extraction, and reversed phase high performance liquid chromatography-tandem mass spectrometry, suitable for the extraction and quantitation of both intracellular and extracellular cyanotoxins in sediments as well as pore waters. Recoveries of nine microcystins, representing the chemical diversity of microcystins, and nodularin (a marine analogue) ranged between 75 and 98% with one, microcystin-RR (MC-RR), at 50%. Chromatographic separation of these analytes was achieved within 7.5 min and the method detection limits were between 1.1 and 2.5 ng g{sup −1} dry weight (dw). The robustness of the method was demonstrated on sediment cores collected from seven Canadian lakes of diverse geography and trophic states. Individual microcystin variants reached a maximum concentration of 829 ng g{sup −1} dw on sediment particles and 132 ng mL{sup −1} in pore waters and could be detected in sediments as deep as 41 cm (>100 years in age). MC-LR, -RR, and -LA were more often detected while MC-YR, -LY, -LF, and -LW were less common. The analytical method enabled us to estimate sediment-pore water

  8. Method for analyzing solvent extracted sponge core

    Energy Technology Data Exchange (ETDEWEB)

    Ellington, W.E.; Calkin, C.L.

    1988-11-22

    For use in solvent extracted sponge core measurements of the oil saturation of earth formations, a method is described for quantifying the volume of oil in the fluids resulting from such extraction. The method consists of: (a) separating the solvent/oil mixture from the water in the extracted fluids, (b) distilling at least a portion of the solvent from the solvent/oil mixture substantially without co-distillation or loss of the light hydrocarbons in the mixture, (c) determining the volume contribution of the solvent remaining in the mixture, and (d) determining the volume of oil removed from the sponge by substracting the determined remaining solvent volume.

  9. Simultaneous analysis of organochlorine pesticides and polychlorinated biphenyls in air samples by using accelerated solvent extraction (ASE) and solid-phase micro-extraction (SPME) coupled to gas chromatography dual electron capture detection.

    Science.gov (United States)

    Mokbel, Haifaa; Al Dine, Enaam Jamal; Elmoll, Ahmad; Liaud, Céline; Millet, Maurice

    2016-04-01

    An analytical method associating accelerated solvent extraction (ASE) and solid-phase micro-extraction (SPME) in immersion mode combined with gas chromatography dual electrons capture detectors (SPME-GC-2ECD) has been developed and studied for the simultaneous determination of 19 organochlorine pesticides (OCPs) and 22 polychlorinated biphenyls (PCBs) in air samples (active and XAD-2 passive samplers). Samples were extracted with ASE with acetonitrile using the following conditions: temperature, 150 °C; pressure, 1500 psi; static, 15 min; cycles, 3; purge, 300 s; flush, 100 %. Extracts were reduced to 1 mL, and 500 μL of this extract, filled with deionised water, was subject to SPME extraction. Experimental results indicated that the proposed method attained the best extraction efficiency under the optimised conditions: extraction of PCB-OCP mixture using 100-μm PDMS fibre at 80 °C for 40 min with no addition of salt. The performance of the proposed ASE-SPME-GC-2ECD methodology with respect to linearity, limit of quantification and detection was evaluated by spiking of XAD-2 resin with target compounds. The regression coefficient (R (2)) of most compounds was found to be high of 0.99. limits of detection (LODs) are between 0.02 and 4.90 ng m(-3), and limits of quantification (LOQs) are between 0.05 and 9.12 ng m(-3) and between 0.2 and 49 ng/sampler and 0.52 and 91 ng/sampler, respectively, for XAD-2 passive samplers. Finally, a developed procedure was applied to determine selected PCBs and OCPs in the atmosphere.

  10. A new procedure combining GC-MS with accelerated solvent extraction for the analysis of phthalic acid esters in contaminated soils

    Institute of Scientific and Technical Information of China (English)

    Tingting MA; Ying TENG; Peter CHRISTIE; Yongming LUO; Yongshan CHEN; Mao YE

    2013-01-01

    An optimized procedure based on gas chromatography-mass spectrometry (GC-MS) combined with accelerated solvent extraction (ASE) is developed for the analysis of six phthalic acid esters (PAEs), which are priority soil pollutants nominated by United States Environmental Protection Agency (USEPA). Quantification of PAEs in soil employs ultrasonic extraction (UE) (USEPA 3550) and ASE (USEPA 3545), followed by clean up procedures involving three different chromatography columns and two combined elution methods. GC-MS conditions under selected ion monitoring (SIM) mode are described and quality assurance and quality control (QA/ QC) criteria with high accuracy and sensitivity for target analytes were achieved. Method reliability is assured with the use of an isotopically labeled PAE, di-n-butyl phthalate-d4 (DnBP-D4), as a surrogate, and benzyl benzoate (BB) as an internal standard, and with the analysis of certified reference materials (CRM). QA/QC for the developed procedure was tested in four PAE-spiked soils and one PAE-contaminated soil. The four spiked soils were originated from typical Chinese agricultural fields and the contaminated soil was obtained from an electronic waste dismantling area. Instrument detection limits (IDLs) for the six PAEs ranged 0.10-0.31 μg·L-1 and method detection limits (MDLs) of the four spiked soils varied from a range of 20-70 μg· kg -1 to a range of 90-290 μg· kg-1. Lineal-iVy of response between 20 μg· L-1 and 2mg.L~ was also established and the correlation coefficients (R) were a11〉0.998. Spiked soil matrix showed relative recovery rates between 75 and 120% for the six target compounds and about 93% for the surrogate substance. The developed procedure is anticipated to be highly applicable for field surveys of soil PAE pollution in China.

  11. Comparison of Extraction Techniques with Different Solvents for DDT Analogues in Sediments

    Institute of Scientific and Technical Information of China (English)

    LANG Yin-Hai; JIANG Xin; D. MARTENS; ZHAO Qi-Guo

    2005-01-01

    Four techniques, Soxhlet extraction (SOX), ultrasonic extraction (USE), fluidized-bed extraction (FBE) and accelerated solvent extraction (ASE) with different solvents (methanol, hexane/acetone and acetonitrile) were used for the extraction of DDT analogues in sediments. Results revealed that the four extraction techniques had high recoveries (>86.0%) with low standard deviations (< 12.0%) for most of DDT analogues, meaning that they could all successfully extract DDT analogues in sediments. Accelerated solvent extraction using methanol and hexane/acetone (1:1), fluidized-bed extraction using hexane/acetone (1:1) and the ultrasonic extraction using hexane/acetone (1:1) were comparable or better than Soxhlet extraction using hexane/acetone (1:1). Considering solvent- and time-consumption, level of automation,and environmental risk, accelerated solvent extraction with hexane/acetone (1:1) was better than the other extraction techniques.

  12. Improved Supercritical-Solvent Extraction of Coal

    Science.gov (United States)

    Compton, L.

    1982-01-01

    Raw coal upgraded by supercritical-solvent extraction system that uses two materials instead of one. System achieved extraction yields of 20 to 49 weight percent. Single-solvent yields are about 25 weight percent. Experimental results show extraction yields may be timedependent. Observed decreases in weight of coal agreed well with increases in ash content of residue.

  13. Improved efficiency of extraction of polycyclic aromatic hydrocarbons (PAHs) from the National Institute of Standards and Technology (NIST) Standard Reference Material Diesel Particulate Matter (SRM 2975) using accelerated solvent extraction.

    Science.gov (United States)

    Masala, Silvia; Ahmed, Trifa; Bergvall, Christoffer; Westerholm, Roger

    2011-12-01

    The efficiency of extraction of polycyclic aromatic hydrocarbons (PAHs) with molecular masses of 252, 276, 278, 300, and 302 Da from standard reference material diesel particulate matter (SRM 2975) has been investigated using accelerated solvent extraction (ASE) with dichloromethane, toluene, methanol, and mixtures of toluene and methanol. Extraction of SRM 2975 using toluene/methanol (9:1, v/v) at maximum instrumental settings (200 °C, 20.7 MPa, and five extraction cycles) with 30-min extraction times resulted in the following elevations of the measured concentration when compared with the certified and reference concentrations reported by the National Institute of Standards and Technology (NIST): benzo[b]fluoranthene, 46%; benzo[k]fluoranthene, 137%; benzo[e]pyrene, 103%; benzo[a]pyrene, 1,570%; perylene, 37%; indeno[1,2,3-cd]pyrene, 41%; benzo[ghi]perylene, 163%; and coronene, 361%. The concentrations of the following PAHs were comparable to the reference values assigned by NIST: indeno[1,2,3-cd]fluoranthene, dibenz[a,h]anthracene, and picene. The measured concentration of dibenzo[a,e]-pyrene was lower than the information value reported by the NIST. The measured concentrations of other highly carcinogenic PAHs (dibenzo[a,l]pyrene, dibenzo[a,i]pyrene, and dibenzo[a,h]pyrene) in SRM 2975 are also reported. Comparison of measurements using the optimized ASE method and using similar conditions to those applied by the NIST for the assignment of PAH concentrations in SRM 2975 indicated that the higher values obtained in the present study were associated with more complete extraction of PAHs from the diesel particulate material. Re-extraction of the particulate samples demonstrated that the deuterated internal standards were more readily recovered than the native PAHs, which may explain the lower values reported by the NIST. The analytical results obtained in the study demonstrated that the efficient extraction of PAHs from SRM 2975 is a critical requirement for the

  14. Extractive Distillation with Salt in Solvent

    Institute of Scientific and Technical Information of China (English)

    1999-01-01

    Extractive distillation with salt in solvent is a new process for producing anhydrous ethanol by combining the principle of "salt effect" and some traditional extractive distillation methods. Compared with the common extractive distillation the performance of solvent is improved, the recycling amount of solvent is reduced to 1/4-1/5, and the number of theoretical plates is reduced to 1/3. Energy consumption and cost of equipment are also reduced and continuous production is realized. High efficiency and low solvent wastage make this technique feasible.

  15. Supercritical-Multiple-Solvent Extraction From Coal

    Science.gov (United States)

    Corcoran, W.; Fong, W.; Pichaichanarong, P.; Chan, P.; Lawson, D.

    1983-01-01

    Large and small molecules dissolve different constituents. Experimental apparatus used to test supercritical extraction of hydrogen rich compounds from coal in various organic solvents. In decreasing order of importance, relevant process parameters were found to be temperature, solvent type, pressure, and residence time.

  16. Combination of accelerated solvent extraction and vortex-assisted liquid-liquid microextraction for the determination of dimethyl fumarate in textiles and leathers by gas chromatography-mass spectrometry.

    Science.gov (United States)

    Lu, Yang; Zhu, Yan

    2014-02-01

    A simple and environmentally friendly sample preparation procedure coupled with gas chromatography-mass spectrometry was developed to assay dimethyl fumarate in textiles and leathers. The sample preparation procedure involved an accelerated solvent extraction (ASE) using water as the extract solvent, followed by the extraction and concentration of dimethyl fumarate from the aqueous solution using vortex-assisted liquid-liquid microextraction (VALLME). The parameters affecting the ASE and VALLME were optimized to achieve the maximum extraction efficiency, and the performance of the developed method was evaluated. Good linearity was observed over the range assayed (0.01-1mg/kg) with a regression coefficient of 0.998. The limit of detection and enrichment factor for the VALLME step were 0.001 mg/kg and 53, respectively. The intra- and inter-day precision were below 8.9%, and the recovery was approximately 84-103%. The as-developed method was successfully applied to textiles and leather samples.

  17. Solvent Extraction Developments in Southern Africa

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The largest solvent-extraction plant in the world at the time, the Nchanga Copper Operation, was in Zambia. The first commercial process using solvent extraction for the refining of the platinum-group metals was in South Africa. More recently, the Southern African region has seen the implementation of solvent extraction for other base metals, precious metals, and specialty metals. These include the world firsts of primary production of zinc at Skorpion Zinc in Namibia and the large-scale refining of gold by Harmony Gold in South Africa. Several other flowsheets that use solvent-extraction technology are currently under commissioning, development, or feasibility study for implementation in this part of the world, including those for the recovery of copper, cobalt, nickel, tantalum, and niobium.

  18. Online cleanup of accelerated solvent extractions for determination of adenosine 5'-triphosphate (ATP), adenosine 5'-diphosphate (ADP), and adenosine 5'-monophosphate (AMP) in royal jelly using high-performance liquid chromatography.

    Science.gov (United States)

    Xue, Xiaofeng; Wang, Feng; Zhou, Jinhui; Chen, Fang; Li, Yi; Zhao, Jing

    2009-06-10

    Determination of the levels of adenosine 5'-triphosphate (ATP), adenosine 5'-diphosphate (ADP), and adenosine 5'-monophosphate (AMP) in royal jelly is important for the study of its pharmacological activities, health benefits, and adenosine phosphate degradation. In this study was developed a novel method to determine ATP, ADP, and AMP levels in royal jelly using accelerated solvent extraction (ASE) followed by online cleanup and high-performance liquid chromatography (HPLC) with diode array detection (DAD). The optimum extraction conditions were obtained using an 11 mL ASE cell, ethanol/water (5:5 v/v) as the extraction solvent, 1500 psi, 80 degrees C, a 5 min static time, and a 60% flush volume. Optimum separation of the three compounds was achieved in AMP levels in 15 samples of royal jelly of different origins was performed. Sample results indicated that the AMP concentration was 24.2-2214.4 mg kg(-1), whereas ATP and ADP were not detectable or present only at low levels.

  19. Solvent extraction:The coordination chemistry behind extractive metallurgy

    OpenAIRE

    2014-01-01

    The modes of action of the commercial solvent extractants used in extractive hydrometallurgy are classified according to whether the recovery process involves the transport of metal cations, Mn+, metalate anions, MXxn-, or metal salts, MXx into a water-immiscible solvent. Well-established principles of coordination chemistry provide an explanation for the remarkable strengths and selectivities shown by most of these extractants. Reagents which achieve high selectivity when transporting metal ...

  20. Application of accelerated solvent extraction in analysis of aromatic compounds in tobacco%加速溶剂萃取法在烟草香气分析中的应用

    Institute of Scientific and Technical Information of China (English)

    朱晓兰; 黄兰; 李盼盼; 高芸; 杨俊

    2011-01-01

    The accelerated solvent extraction (ASE) was used to extract aromatic compounds in tobacco, and more than 10 aldehydes and ketones were identified and determined by gas chromatography/mass spec-trometry. The optimum conditions for ASE (heating time? Solvent volume and extraction time) were investigated with orthogonal array design. The results of ASE and simultaneous distillation extraction (SDE) were compared. The results indicate that the ASE is simple, rapid and easy-to -operate, its repeatability is satisfactory, and the recoveries are in the range of 80. 3%~106. 4%. The ASE is a little better than SDE.%通过加速溶剂萃取法分离烟草中的香味物质,对烟草中10多种醛酮类香味物质用GC/MS进行定性分析,并用内标法进行定量分析,采用正交实验方案探讨了加速溶剂萃取分离烟草香味物质的优化条件,比较了该方法与同时蒸馏萃取对分析结果的影响.结果显示:加速溶剂萃取简便、快速,易于操作,重复性令人满意,回收率范围是80.3%~106.4%,比同时蒸馏萃取法略好.

  1. [Determination of 19 antibiotic and 2 sulfonamide metabolite residues in wild fish muscle in mariculture areas of Laizhou Bay using accelerated solvent extraction and high performance liquid chromatography-tandem mass spectrometry].

    Science.gov (United States)

    Liu, Sisi; Du, Juan; Chen, Jingwen; Zhao, Hongxia

    2014-12-01

    A sample preparation and analytical method with accelerated solvent extraction (ASE) and high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/ MS) was developed to detect 19 antibiotic (9 sulfonamides, 4 quinolones, 3 macrolides and 3 others) and 2 sulfonamide metabolite residues in fish muscle. The target compounds were extracted using ASE and purified simultaneously by a C18 resin in the extraction cell. The extracts were evaporated to dryness, and redissolved with the initial mobile phase for HPLC-MS/MS analysis after freezing centrifugation (10,000 r/min, -4 °C) to remove the fat and other matrix compounds further. The separation of the analytes was carried out on an Xterra MS C18 column with methanol-acetonitrile (1:1, v/v) as mobile phase A and 0. 1% formic acid (containing 0. 1% ammonium formate) as mobile phase B. The spiked recoveries of the method were 55. 2%-113. 3%, with the relative standard deviations of 0. 1% - 17. 6% (n = 6). The limits of detection ranged from 0. 003 to 0. 6 ng/g. The method was applied to two fish (Synechogobius hasta and Liza haematocheilus) collected in mariculture areas of Laizhou Bay and six antibiotics were detected, in which the mass concentrations of norfloxacin were highest with mean values of 67. 01 and 27. 58 ng/g, respectively. The method is simple, rapid, highly sensitive, and useful in the study on exposure levels and environmental behavior of the antibiotics.

  2. 加速溶剂萃取GC-NCI-MS法测定糙米中氯硝胺残留量%Detection of Dicloran Residue in Crude Rice by the Combination of Accelerated Solvent Extraction and GC-NCI-MS

    Institute of Scientific and Technical Information of China (English)

    何理; 吴晖

    2012-01-01

    [目的]建立一种采用加速溶剂萃取和气相色谱-质谱测定糙米中氯硝胺残留量的分析方法.[方法]试样采用丙酮-正己烷(体积比1:2)萃取,中性氧化铝固相萃取小柱净化.用HP-FFAP石英毛细管柱程序升温分离,GC-NCI-MS的选择离子监测方式(SIM)测定,外标法定量.并对提取溶剂、萃取温度、不同冲洗体积、静态萃取时间和循环次数等试验条件进行优化.[结果]当添加水平为1、2、10、20、100 μg/kg时,方法回收率为93.6% ~ 102.8%,相对标准偏差为2.2%~6.2%,检出限是1μg/kg.采用保留时间和选择监视离子丰度比对阳性样品进行确证,加速溶剂萃取法和固相萃取技术净化糙米中氯硝胺减少了分析时间和溶剂消耗.[结论]试验成功建立了GC-NC-MS的选择离子监测的测定方法测定糙米中氯硝胺残留量,有效地减少基质杂质对分析灵敏度和方法检出限的影响,提高了检测方法的特异性.%[Objective] To establish a new method of accelerated solvent extraction and gas chromatography mass spectrography to determine the dicloran residue in kown rice. [ Method] The sample was extracted by hexane-acetone (1: 2 by volume) , purified by neutral alumina solid phase extraction column, separated by HP-FFAP silica capillary column with temperature programmed, assessed by GC-NCI-MS in selected ion monitoring mode (SIM) , and quantified by external standard. The experimental conditions including extraction solvent, extraction temperature , different flush volume, static extraction time and cycle number have been optimized. [ Result] When the adding level is 1, 2, 10, 20, 100 μg/kg, the method recovery is 93.6% -102.8% ; the relative standard deviation is 2.2% -6.2% and the detection limit is 1 |xg/kg. The result was determined by comparison to positive sample with retention time and selectively monitoring ion abundances. The accelerated solvent extraction and GC-NCI-MS method purified the

  3. Solvent extraction of metals with hydroxamic acids.

    Science.gov (United States)

    Vernon, F; Khorassani, J H

    1978-07-01

    Solvent extraction with hydroxamic acids has been investigated. with comparison of aliphatic and aromatic reagents for the extraction of iron, copper, cobalt and nickel. Caprylohydroxamic acid has been evaluated for use in extraction systems for titanium, vanadium, chromium, molybdenum and uranium, both in terms of acidity of aqueous phase and oxidation state of the metal. It has been established that caprylohydroxamic acid in 1-hexanol is a suitable extractant for the removal of titanium(IV), vanadium(V), chromium(VI), molybdenum(VI) and uranium(VI) from 6M hydrochloric acid.

  4. Accelerating DSMC data extraction.

    Energy Technology Data Exchange (ETDEWEB)

    Gallis, Michail A.; Piekos, Edward Stanley

    2006-10-01

    In many direct simulation Monte Carlo (DSMC) simulations, the majority of computation time is consumed after the flowfield reaches a steady state. This situation occurs when the desired output quantities are small compared to the background fluctuations. For example, gas flows in many microelectromechanical systems (MEMS) have mean speeds more than two orders of magnitude smaller than the thermal speeds of the molecules themselves. The current solution to this problem is to collect sufficient samples to achieve the desired resolution. This can be an arduous process because the error is inversely proportional to the square root of the number of samples so we must, for example, quadruple the samples to cut the error in half. This work is intended to improve this situation by employing more advanced techniques, from fields other than solely statistics, for determining the output quantities. Our strategy centers on exploiting information neglected by current techniques, which collect moments in each cell without regard to one another, values in neighboring cells, nor their evolution in time. Unlike many previous acceleration techniques that modify the method itself, the techniques examined in this work strictly post-process so they may be applied to any DSMC code without affecting its fidelity or generality. Many potential methods are drawn from successful applications in a diverse range of areas, from ultrasound imaging to financial market analysis. The most promising methods exploit relationships between variables in space, which always exist in DSMC due to the absence of shocks. Disparate techniques were shown to produce similar error reductions, suggesting that the results shown in this report may be typical of what is possible using these methods. Sample count reduction factors of approximately three to five were found to be typical, although factors exceeding ten were shown on some variables under some techniques.

  5. Comprehensive multiresidue method for the simultaneous determination of 74 pesticides and metabolites in traditional Chinese herbal medicines by accelerated solvent extraction with high-performance liquid chromatography/tandem mass spectrometry.

    Science.gov (United States)

    Jia, Zhengwei; Mao, Xiuhong; Chen, Ke; Wang, Ke; Ji, Shen

    2010-01-01

    In this paper, a multiresidue method for the simultaneous target analysis of 74 pesticides and metabolites in traditional Chinese herbal medicines (TCHMs) was developed using accelerated solvent extraction (ASE) coupled with HPLC/MS/MS. Pesticide residues were extracted from the different samples using ASE, then purified by gel permeation chromatography and graphitized carbon black/primary, secondary amine SPE. Gradient elution was used in conjunction with positive mode electrospray ionization MS/MS to detect 74 pesticides and metabolites from Cortex Cinnamomi, Flos Carthami, Folium Ginkgo, Herba Pogostemonis, Radix Ginseng, and Semen Ginkgo using a single chromatographic run. The analytical performance was demonstrated by the analysis of extracts spiked at three concentration levels ranging from 0.005 to 0.125 mg/kg for each pesticide and metabolite. In general, recoveries ranging from 70 to 110%, with RSDs better than 15%, were obtained. The recovery and repeatability data were in good accordance with European Union guidelines for pesticide residue analysis. The LOD for most of the targeted pesticides and metabolites tested was below 0.01 mg/kg.

  6. Organic solvents in electromembrane extraction: recent insights

    DEFF Research Database (Denmark)

    Huang, Chuixiu; Gjelstad, Astrid; Pedersen-Bjergaard, Stig

    2016-01-01

    Electromembrane extraction (EME) was invented in 2006 as a miniaturized sample preparation technique for the separation of ionized species from aqueous samples. This concept has been investigated in different areas of analytical chemistry by different research groups worldwide since the introduct......Electromembrane extraction (EME) was invented in 2006 as a miniaturized sample preparation technique for the separation of ionized species from aqueous samples. This concept has been investigated in different areas of analytical chemistry by different research groups worldwide since...... the introduction. Under the influence of an electrical field, EME is based on electrokinetic migration of the analytes through a supported liquid membrane (SLM), which is an organic solvent immobilized in the pores of the polymeric membrane, and into the acceptor solution. Up to date, close to 150 research...... articles with focus on EME have been published. The current review summarizes the performance of EME with different organic solvents and discusses several criteria for efficient solvents in EME. In addition, the authors highlight their personal perspective about the most promising organic solvents for EME...

  7. Solvent

    OpenAIRE

    Hamida Y. Mostafa; Ebaa A. El-Shamy; Amal S. Farag; Nadia G. Kandile

    2013-01-01

    Neat ethylacetoacetate (EAA) and its mixtures with a co-solvent and an anti-solvent have been studied for refining of heavy wax distillate fraction to produce substantially non-carcinogenic base oil. The co-solvent and anti-solvent used are dipropylene glycol (DPG) and ethylene glycol (EG) respectively. The solubility characteristics of the main solvent and its mixed solvent systems were studied. Selection of the optimum solvent mixture and extraction variables has been studied. The effect of...

  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. Solvent extraction: the coordination chemistry behind extractive metallurgy.

    Science.gov (United States)

    Wilson, A Matthew; Bailey, Phillip J; Tasker, Peter A; Turkington, Jennifer R; Grant, Richard A; Love, Jason B

    2014-01-07

    The modes of action of the commercial solvent extractants used in extractive hydrometallurgy are classified according to whether the recovery process involves the transport of metal cations, M(n+), metalate anions, MXx(n-), or metal salts, MXx into a water-immiscible solvent. Well-established principles of coordination chemistry provide an explanation for the remarkable strengths and selectivities shown by most of these extractants. Reagents which achieve high selectivity when transporting metal cations or metal salts into a water-immiscible solvent usually operate in the inner coordination sphere of the metal and provide donor atom types or dispositions which favour the formation of particularly stable neutral complexes that have high solubility in the hydrocarbons commonly used in recovery processes. In the extraction of metalates, the structures of the neutral assemblies formed in the water-immiscible phase are usually not well defined and the cationic reagents can be assumed to operate in the outer coordination spheres. The formation of secondary bonds in the outer sphere using, for example, electrostatic or H-bonding interactions are favoured by the low polarity of the water-immiscible solvents.

  10. Green solvents and technologies for oil extraction from oilseeds.

    Science.gov (United States)

    Kumar, S P Jeevan; Prasad, S Rajendra; Banerjee, Rintu; Agarwal, Dinesh K; Kulkarni, Kalyani S; Ramesh, K V

    2017-01-01

    Oilseeds are crucial for the nutritional security of the global population. The conventional technology used for oil extraction from oilseeds is by solvent extraction. In solvent extraction, n-hexane is used as a solvent for its attributes such as simple recovery, non-polar nature, low latent heat of vaporization (330 kJ/kg) and high selectivity to solvents. However, usage of hexane as a solvent has lead to several repercussions such as air pollution, toxicity and harmfulness that prompted to look for alternative options. To circumvent the problem, green solvents could be a promising approach to replace solvent extraction. In this review, green solvents and technology like aqueous assisted enzyme extraction are better solution for oil extraction from oilseeds. Enzyme mediated extraction is eco-friendly, can obtain higher yields, cost-effective and aids in obtaining co-products without any damage. Enzyme technology has great potential for oil extraction in oilseed industry. Similarly, green solvents such as terpenes and ionic liquids have tremendous solvent properties that enable to extract the oil in eco-friendly manner. These green solvents and technologies are considered green owing to the attributes of energy reduction, eco-friendliness, non-toxicity and non-harmfulness. Hence, the review is mainly focussed on the prospects and challenges of green solvents and technology as the best option to replace the conventional methods without compromising the quality of the extracted products.

  11. Determination of thiamethoxam in vegetables by accelerated solvent extraction-HPLC%快速溶剂萃取高效液相色谱法测定蔬菜中噻虫嗪残留量

    Institute of Scientific and Technical Information of China (English)

    金党琴; 丁邦东; 孔勇

    2014-01-01

    We develop a method for the determination of thiamethoxam in vegetable by accelerated sol-vent extraction-HPLC .The method includes the C18 liquid phase chromatography column ,acetonitrile/phosphate (30 :70 ,by volume)(pH≈3 .0) as the mobile phase ,and the UV detector at 263 nm .The linear correlation is 0 .99993 .Recovery rates with standard samples are 95 .24%-99 .91% .Relative standard devi-ation(RSD) is<3% .The method is rapid ,simple ,and readily applicable the rapid determination of thia-methoxam pesticide in vegetable .%建立了蔬菜中噻虫嗪残留量快速溶剂萃取高效液相色谱的分析方法。使用C18液相色谱柱,以乙腈∶磷酸溶液为流动相,对其进行了定性定量分析,方法的线性相关系数0.99993,加标回收率≥95.24%,相对标准偏差小于3%,该方法步骤简单快速,适用于蔬菜中噻虫嗪农药的快速检测。

  12. Solvent-Controlled Acceleration of Electron Transfer in Binary Mixtures

    NARCIS (Netherlands)

    Pugžlys, Audrius; Hartog, Harald P. den; Baltuška, Andrius; Pshenichnikov, Maxim S.; Umapathy, Siva; Wiersma, Douwe A.

    2001-01-01

    We report a 5-fold acceleration of the backward intermolecular electron transfer between a rhodamine 800 dye molecule and N,N-dimethylaniline (DMA). This effect results from the controlled variation of the solvent dynamical properties in binary mixtures of DMA and acetonitrile. The observed

  13. Development of deep eutectic solvents applied in extraction and separation.

    Science.gov (United States)

    Li, Xiaoxia; Row, Kyung Ho

    2016-09-01

    Deep eutectic solvents, as an alternative to ionic liquids, have greener credentials than ionic liquids, and have attracted considerable attention in related chemical research. Deep eutectic solvents have attracted increasing attention in chemistry for the extraction and separation of various target compounds from natural products. This review highlights the preparation of deep eutectic solvents, unique properties of deep eutectic solvents, and synthesis of deep-eutectic-solvent-based materials. On the other hand, application in the extraction and separation of deep eutectic solvents is also included in this report. In this paper, the available data and references in this field are reviewed to summarize the applications and developments of deep eutectic solvents. Based on the development of deep eutectic solvents, an exploitation of new deep eutectic solvents and deep eutectic solvents-based materials is expected to diversify into extraction and separation. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  14. Improvement of Soybean Oil Solvent Extraction through Enzymatic Pretreatment

    Directory of Open Access Journals (Sweden)

    F. V. Grasso

    2012-01-01

    Full Text Available The purpose of this study is to evaluate multienzyme hydrolysis as a pretreatment option to improve soybean oil solvent extraction and its eventual adaptation to conventional processes. Enzymatic action causes the degradation of the cell structures that contain oil. Improvements in terms of extraction, yield, and extraction rate are expected to be achieved. Soybean flakes and collets were used as materials and hexane was used as a solvent. Temperature, pH, and incubation time were optimized and diffusion coefficients were estimated for each solid. Extractions were carried out in a column, oil content was determined according to time, and a mathematical model was developed to describe the system. The optimum conditions obtained were pH 5.4, 38°C, and 9.7 h, and pH 5.8, 44°C, and 5.8h of treatment for flakes and collets, respectively. Hydrolyzed solids exhibited a higher yield. Diffusion coefficients were estimated between 10-11 and 10-10. The highest diffusion coefficient was obtained for hydrolyzed collets. 0.73 g oil/mL and 0.7 g oil/mL were obtained at 240 s in a column for collets and flakes, respectively. Hydrolyzed solids exhibited a higher yield. The enzymatic incubation accelerates the extraction rate and allows for higher yield. The proposed model proved to be appropriate.

  15. SOLVENT EXTRACTION OF GINGER OLEORESIN USING ULTRASOUND

    Directory of Open Access Journals (Sweden)

    Normalina Arpi

    2011-11-01

    Full Text Available The use of ultrasound in extraction process creates novel and interesting methodologies, which are oftencomplementary to conventional extraction methods. In the present study, the use of ultrasound to extract oleoresin fromginger (Zingiber officinale R. was investigated. The extraction was performed by using ethanol as solvent in thepresence of ultrasonic irradiations operating at frequency of 42 kHz at extraction temperature of 60 oC. The oleoresinextracted was in the form of dark thick liquid with specific ginger flavor. Based on GC-MS analysis, the use ofultrasound was not give an effect on alteration of main component in ginger oleoresin. The main component inextracted ginger oleoresin was zingerone. Gingerol as one of the pungent principle of the ginger oleoresin was notdetected due to decomposition of gingerol at a temperature above 45 oC. Extraction rate of ultrasound-assistedextraction was about 1.75 times more rapid than a conventional system based on soxhlet. The scanning electronmicroscopy images provided more evidence for the mechanical effects of ultrasound, mainly appearing on cells’ wallsand shown by the destruction of cells, facilitating the release of their contents.

  16. PULSED MIXER-SETTLER SOLVENT EXTRACTION CONTACTORS

    Science.gov (United States)

    Figg, W.S.

    1958-08-12

    A mixer-settler extractor is described for contacting immiscible liquids having different specific gravities in order to withdraw one or more components from one liquid with the aid of the other liquid. The extractor consists of a hollow column, a rotary drive shafi extending : through the column with a number of impellers spaced thereon, an equal nunnber of separator plate sets each consisting of one fluorothene and one stainless steel plate with peripheral recesses and flow slots mounted on the column, and a pulse generator. This apparatus is particularly useful in solvent extraction processes for recovering plutonium from aqueous acidic solutions of irradiated uranium.

  17. Solvent extraction of Southern US tar sands

    Energy Technology Data Exchange (ETDEWEB)

    Penney, W.R.

    1990-01-01

    The Department of Chemical Engineering at the University of Arkansas, in association with Diversified Petroleum Recovery, Inc. (DPR) of Little Rock, Arkansas, has been developing a solvent extraction process for the recovery of bitumen from tar sands for the past five years. The unique feature of the process is that the bitumen is recovered from the solvent by contacting with a co-solvent, which causes the bitumen to precipitate. The overall purpose of this project is to study both the technical and economic feasibility of applying this technology for recovery of bitumen from tar sands by (1) investigating the socioeconmic factors which affect (a) plant siting and (b) the market value of recovered bitumen; (2) operating a process demonstration unit at the rate of 1 lb/hr recovered bitumen while producing clean sand and recyclable solvents; and (3) determine the economic conditions which will make a bitumen recovery project economical. DPR has analyzed the historical trends of domestic production, consumption, discoveries and reserves of crude oil. They have started an investigation of the volatility in the price of crude oil and of gasoline prices and of the differential between gasoline and crude oil. DPR continues to analyze the geographical movement and demand for asphalt products. Utah does not appear economically attractive as a site for a bitumen from tar sands asphalt plant. Oklahoma sites are now being studied. This report also contains the quarterly progress report from a University of Nevada study to determine bitumen composition, oxygen uptake rates, and viscosities of Alabama and Utah bitumens. Both reports have been indexed separately for inclusion on the data base.

  18. Solvent extraction of Southern US tar sands

    Energy Technology Data Exchange (ETDEWEB)

    Penney, W.R.

    1990-01-01

    The Department of Chemical Engineering at the University of Arkansas, in association with Diversified Petroleum Recovery, Inc. (DPR) of Little Rock, Arkansas, has been developing a solvent extraction process for the recovery of bitumen from tar sands for the past five years. The unique feature of the process is that the bitumen is recovered from the solvent by contacting with a co-solvent, which causes the bitumen to precipitate. The overall purpose of this project is to study both the technical and economic feasibility of applying this technology for recovery of bitumen from tar sands by (1) investigating the socioeconmic factors which affect (a) plant siting and (b) the market value of recovered bitumen; (2) operating a process demonstration unit at the rate of 1 lb/hr recovered bitumen while producing clean sand and recyclable solvents; and (3) determine the economic conditions which will make a bitumen recovery project economical. DPR has analyzed the historical trends of domestic production, consumption, discoveries and reserves of crude oil. They have started an investigation of the volatility in the price of crude oil and of gasoline prices and of the differential between gasoline and crude oil. DPR continues to analyze the geographical movement and demand for asphalt products. Utah does not appear economically attractive as a site for a bitumen from tar sands asphalt plant. Oklahoma sites are now being studied. This report also contains the quarterly progress report from a University of Nevada study to determine bitumen composition, oxygen uptake rates, and viscosities of Alabama and Utah bitumens. Both reports have been indexed separately for inclusion on the data base.

  19. Terpenes as Green Solvents for Extraction of Oil from Microalgae

    OpenAIRE

    Celine Dejoye Tanzi; Maryline Abert Vian; Christian Ginies; Mohamed Elmaataoui; Farid Chemat

    2012-01-01

    Herein is described a green and original alternative procedure for the extraction of oil from microalgae. Extractions were carried out using terpenes obtained from renewable feedstocks as alternative solvents instead of hazardous petroleum solvents such as n-hexane. The described method is achieved in two steps using Soxhlet extraction followed by the elimination of the solvent from the medium using Clevenger distillation in the second step. Oils extracted from microalgae...

  20. Non-Ideal Behavior in Solvent Extraction

    Energy Technology Data Exchange (ETDEWEB)

    Peter Zalupski

    2011-09-01

    This report presents a summary of the work performed to meet FCR&D level 3 milestone M31SW050801, 'Complete the year-end report summarizing FY11 experimental and modeling activities.' This work was carried out under the auspices of the Non-Ideality in Solvent Extraction Systems FCR&D work package. The report summarizes our initial considerations of potential influences that non-ideal chemistry may impose on computational prediction of outcomes in solvent extraction systems. The report is packaged into three separate test cases where a robustness of the prediction by SXFIT program is under scrutiny. The computational exercises presented here emphasize the importance of accurate representation of both an aqueous and organic mixtures when modeling liquid-liquid distribution systems. Case No.1 demonstrates that non-ideal behavior of HDEHP in aliphatic diluents, such as n-dodecane, interferes with the computation. Cases No.2 and No.3 focus on the chemical complexity of aqueous electrolyte mixtures. Both exercises stress the need for an improved thermodynamic model of an aqueous environment present in the europium distribution experiments. Our efforts for year 2 of this project will focus on the improvements of aqueous and non-aqueous solution models using fundamental physical properties of mixtures acquired experimentally in our laboratories.

  1. 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

  2. ASE-GC法测定速冻饺子中有机磷农药残留%Determination of Organophosphrous Pesticides in Frozen Dumplings with Accelerated Solvent Extraction and Chromatography

    Institute of Scientific and Technical Information of China (English)

    孟辉; 汤淳

    2014-01-01

    建立了加速溶剂萃取( ASE)-在线净化-GC法测定速冻饺子中有机磷农药残留量的检测方法。该方法快速、稳定、可靠、操作简便,15种有机磷农药在0.05~0.50μg/mL范围内线性良好,相关系数均大于0.9985,最低检测限为0.006~0.050 mg/kg ,样品添加回收率在84.88%~107.10%之间,相对标准偏差(RSD)为1.92%~14.0%,适用于速冻馅类食品中有机磷农药残留的检测与确定。%A accelerated solvent extraction ( ASE ) and online purification method to determine the organo-phosphrous pesticide residues in frozen dumplings was established .With high speed , stability , reliability and easy operation, this method obtained good linearity for determining 15 pesticides with concentration between 0.05-0.5μg/mL (the correlation coefficients (r) were all greater than 0.998 5).The detection limits ranged from 0.006 mg/kg to 0.05mg/kg.The average recoveries of organophosphrous pesticides were between 84.88%and 107.1%. The relative standard deviations for 15 organophosphrous pesticides were between 1.92%and 1.40%.

  3. Optimisation and application of accelerated solvent extraction and flash chromatography for quantification of PCBs in tree barks and XAD-2 passive samplers using GC-ECD with dual columns.

    Science.gov (United States)

    Guéguen, Florence; Stille, Peter; Millet, Maurice

    2013-07-15

    An analytical method for the quantification of Polychlorinated biphenyls (PCBs) concentrations in XAD-2 passive air samplers (PAS) and tree barks collected close to the Rhine River between France and Germany was developed. This method used Accelerated Solvent Extraction (ASE) followed by a purification step by flash chromatography using a 4gr cartridge (3 g of silica gel and 1 g of 44% acidified silica) and analysis by GC-ECD with dual columns. Quantification (QL) and detection (DL) limits varied 0.5 from and 5.7 ng PAS(-1) and from 0.5 and 3.0 ng PAS(-1) respectively. For tree barks, quantification and detection limits were calculated for each congener on washed tree bark sample with a signal to noise ratio of 3:1 and 10:1 (corresponding to a LQ in the range of 1-4 ng per bark sample by congeners). Uncertainties on each congener concentration were calculated to be in the range of 3-20% XAD-2 passive samplers were field calibrated by using Hi-vol. Samplers. Sampling rates of 4.2, 11.5, 1.6, and 7.9 m(3) PAS(-1) d(-1) for tri-, tetra-, penta- hexa-PCBs, respectively were obtained and are comparable to those already obtained with PUF-PAS for gas phase only (gas/particle distribution was 90/10). Method was applied to real atmospheric samples collected by XAD-2 passive samplers and tree barks in the east of France.

  4. Study on Accelerated Solvent Extraction of Free Fatty Acids in Marine Sediments%加速溶剂萃取技术提取海洋沉积物中游离态脂肪酸的方法研究

    Institute of Scientific and Technical Information of China (English)

    李小琳; 贺行良; 李凤; 张媛媛; 陈立雷; 张培玉

    2014-01-01

    脂肪酸是沉积物中含量最丰富的脂类标记物之一,其存在形式主要有游离态脂肪酸和结合态脂肪酸。游离态脂肪酸可由溶剂直接提取,结合态脂肪酸是在已提取出游离态脂肪酸的沉积物残渣中加入酸碱加热后再用溶剂提取。加速溶剂萃取技术(ASE )因成本低和操作毒性小,在脂肪酸研究中得到了广泛的应用。本文采集东海近海海域沉积物作为研究样本,由于其中游离态脂肪酸含量丰富,而结合态脂肪酸含量过低,测定结果精密度差,难以作为方法研究对象,因此主要针对游离态脂肪酸应用ASE 法进行提取,研究了各种实验条件,包括萃取剂、萃取温度、静态萃取时间和循环次数的选择与优化。分析结果表明,甲醇-二氯甲烷(V/V,1∶3)更适合作为萃取剂;随着萃取温度、静态萃取时间、循环次数的增加,不同类型脂肪酸的提取效率各不相同,以涵盖碳原子数最多为先决条件,以脂肪酸的萃取效率最大化为依据,确定了ASE的实验条件是:萃取温度110℃,静态提取时间10 min,循环3次。用这种处理方法5次测定沉积物样品中大部分游离态脂肪酸的精密度为3.3%~19.0%,其替代物回收率为72.2%~104.6%。该方法应用于分析实际海洋沉积物样品,相比于传统的索氏提取法,流程简单,极大地提高了工作效率。%Fatty acids are one of the most abundant lipid markers in marine sediments,whose primary occurrence forms are free fatty acids and conjugated fatty acid.Free fatty acid can be extracted directly by solvent,and conjugated fatty acid is extracted from leftover sediment residue after free fatty acid has been extracted,through adding acid or alkali,and then extracting after being heated.Accelerated Solven Extraction (ASE)is a very popular method in the study of fatty acids due to its low cost and low toxicity

  5. Solvent Extraction in Hydrometallurgy: Present and Future

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    During the past 10 years, there have been incremental advances in the application of solvent extraction to process hydrometallurgy. The most cited areas in the literature include chemistry, chemical engineering, pilot plants, and plant operation. Within these areas, there were considerable interest in synergism,diluents, degradation, contactors, surfactants, hydrometallurgical applications, environmental and secondary applications, and health and safety. The summary to the present is followed by a prediction for the future in the above areas of interest. These include the use of speciation; improved understanding of the role of surfactants on the system; optimization through modelling, pilot plants, and contactor selection; improvements in plant operation; further new applications; and plant safety. The review has indicated that considerable knowledge is now available to optimize and improve on process design and plant applications.

  6. Terpenes as green solvents for extraction of oil from microalgae.

    Science.gov (United States)

    Dejoye Tanzi, Celine; Abert Vian, Maryline; Ginies, Christian; Elmaataoui, Mohamed; Chemat, Farid

    2012-07-09

    Herein is described a green and original alternative procedure for the extraction of oil from microalgae. Extractions were carried out using terpenes obtained from renewable feedstocks as alternative solvents instead of hazardous petroleum solvents such as n-hexane. The described method is achieved in two steps using Soxhlet extraction followed by the elimination of the solvent from the medium using Clevenger distillation in the second step. Oils extracted from microalgae were compared in terms of qualitative and quantitative determination. No significant difference was obtained between each extract, allowing us to conclude that the proposed method is green, clean and efficient.

  7. Terpenes as Green Solvents for Extraction of Oil from Microalgae

    Directory of Open Access Journals (Sweden)

    Celine Dejoye Tanzi

    2012-07-01

    Full Text Available Herein is described a green and original alternative procedure for the extraction of oil from microalgae. Extractions were carried out using terpenes obtained from renewable feedstocks as alternative solvents instead of hazardous petroleum solvents such as n-hexane. The described method is achieved in two steps using Soxhlet extraction followed by the elimination of the solvent from the medium using Clevenger distillation in the second step. Oils extracted from microalgae were compared in terms of qualitative and quantitative determination. No significant difference was obtained between each extract, allowing us to conclude that the proposed method is green, clean and efficient.

  8. Solvent Extraction of Chemical Attribution Signature Compounds from Painted Wall Board: Final Report

    Energy Technology Data Exchange (ETDEWEB)

    Wahl, Jon H.; Colburn, Heather A.

    2009-10-29

    This report summarizes work that developed a robust solvent extraction procedure for recovery of chemical attribution signature (CAS) compound dimethyl methyl phosphonate (DMMP) (as well as diethyl methyl phosphonate (DEMP), diethyl methyl phosphonothioate (DEMPT), and diisopropyl methyl phosphonate (DIMP)) from painted wall board (PWB), which was selected previously as the exposed media by the chemical attribution scientific working group (CASWG). An accelerated solvent extraction approach was examined to determine the most effective method of extraction from PWB. Three different solvent systems were examined, which varied in solvent strength and polarity (i.e., 1:1 dichloromethane : acetone,100% methanol, and 1% isopropanol in pentane) with a 1:1 methylene chloride : acetone mixture having the most robust and consistent extraction for four original target organophosphorus compounds. The optimum extraction solvent was determined based on the extraction efficiency of the target analytes from spiked painted wallboard as determined by gas chromatography x gas chromatography mass spectrometry (GCxGC-MS) analysis of the extract. An average extraction efficiency of approximately 60% was obtained for these four compounds. The extraction approach was further demonstrated by extracting and detecting the chemical impurities present in neat DMMP that was vapor-deposited onto painted wallboard tickets.

  9. Distribution of multi-component solvents in solvent vapor extraction chamber

    Energy Technology Data Exchange (ETDEWEB)

    Das, S. [Society of Petroleum Engineers, Richardson, TX (United States)]|[Marathon Oil Corp., Houston, TX (United States)

    2008-10-15

    Vapex process performance is sensitive to operating pressures, temperatures and the types of solvent used. The hydrocarbon solvents used in Vapex processes typically have between 5 and 10 per cent hydrocarbon impurities, and the accumulation of dense phases inside the vapor chamber reduces gravity drainage potential. This study investigated the partitioning of solvent compounds inside the vapor chamber during in situ Vapex processes.The aim of the study was to examine how the different components of the mixed solvent partitioned inside the extracted chamber during the oil and vapor phase. A 2-D homogenous reservoir model was used to simulate the Vapex process with a solvent mixture comprised of propane and methane at various percentages. The effect of injecting a hot solvent vapor was also investigated. The study showed that injected methane accumulated at both the top and the extraction interface. Accumulations near the top had a positive impact on solvent confinement in thin reservoirs. Diffusion of the solvent component was controlled by gas phase molecular diffusion, and was much faster than the diffusion of solvent molecules in the liquid phase. The use of hot solvent mixtures slowed the extraction process due to lower solvent solubility in the oil phase. It was concluded that the negative impact on viscosity reduction by dilution was not compensated by rises in temperature. 6 refs., 11 figs.

  10. The use of environmentally sustainable bio-derived solvents in solvent extraction applications-A review

    Institute of Scientific and Technical Information of China (English)

    Zheng Li; Kathryn H. Smith; Geoffrey W. Stevens

    2016-01-01

    Replacement of volatile organic compounds (VOCs) by greener or more environmental y sustainable solvents is becoming increasingly important due to the increasing health and environmental concerns as wel as economic pressures associated with VOCs. Solvents that are derived from biomass, namely bio-derived solvents, are a type of green solvent that have attracted intensive investigations in recent years because of their advantages over con-ventional VOCs, such as low toxicity, biodegradability and renewability. This review aims to summarize the use of bio-derived solvents in solvent extraction applications, with special emphasis given to utilization of biodiesels and terpenes. Compared with the conventional VOCs, the overall performance of these bio-derived solvents is comparable in terms of extraction yields and selectivity for natural product extraction and no difference was found for metal extraction. To date most researchers have focused on laboratory scale thermodynamics studies. Future work is required to develop and test new bio-derived solvents and understand the kinetic performance as well as solvent extraction pilot plant studies.

  11. Solvent Extraction and Characterization of Neutral Lipids in Oocystis sp.

    Directory of Open Access Journals (Sweden)

    Renil eAnthony

    2015-01-01

    Full Text Available Microalgae are a favorable feedstock for bioproducts and biofuels due to their high oil content, fast growth rates and low resource demands. Solvent lipid extraction efficiency from microalgae is dependent on algal strain and the extraction solvent. Four non-polar extraction solvents were evaluated for the recovery of neutral cellular lipids from microalgae Oocystis sp. (UTEX LB2396. Methylene chloride, hexane, diethyl ether, and cyclohexane were selected as the extraction solvents. All solvent extracts contained hexadecanoic acid, linoleic acid and linolenic acid; accounting for 70% of total lipid content with a proportional wt% composition of the three fatty acids, except for the hexane extracts that showed only hexadecanoic acid and linoleic acid. While not statistically differentiated, methylene chloride proved to be the most effective solvent for Oocystis sp. among the four solvents tested with a total average neutral lipid recovery of 0.25% of dry weight followed by diethyl ether (0.18%, cyclohexane (0.14% and hexane (0.11%. This research presents a simple methodology to optimize the selection of lipid specific extraction solvents for the microalgal strain selected.

  12. Ionic liquids and deep eutectic solvents in natural products research: mixtures of solids as extraction solvents.

    Science.gov (United States)

    Dai, Yuntao; van Spronsen, Jaap; Witkamp, Geert-Jan; Verpoorte, Robert; Choi, Young Hae

    2013-11-22

    Mixtures of solid chemicals may become liquid under certain conditions. These liquids are characterized by the formation of strong ionic (ionic liquids) or hydrogen bonds (deep eutectic solvents). Due to their extremely low vapor pressure, they are now widely used in polymer chemistry and synthetic organic chemistry, yet little attention has been paid to their use as extraction solvents of natural products. This review summarizes the preparation of ionic liquids and deep eutectic solvents with natural product components and recent progress in their applications to the extraction and analysis of natural products as well as the recovery of extracted compounds from their extracts. Additionally, various factors affecting extraction features of ionic liquids and deep eutectic solvents, as well as potential useful technologies including microwave and ultrasound to increase the extraction efficiency, are discussed.

  13. Solid-liquid solvent extraction of metal ions

    Institute of Scientific and Technical Information of China (English)

    Bo Peng; Haiyan Fan; Jinzhang Gao

    2003-01-01

    An overview of extraction of some trace metal ions using molten solvent (low melting substance) during last two decadesis presented. The development of this technique since its inception is briefly traced. The comparison of extraction efficiency, thermo-dynamics and kinetics mainly involving extraction of rare earth ions between molten solvent extraction at high temperature and usualliquid-liquid extraction at room temperature are discussed in detail. The various parameters obtained from the previous and presentstudies such as equilibrium extraction constant Kex, pH1/2, thermodynamic and kinetic data are displayed in tabular form. Finally, thecurrent demands, disadvantages and future prospects are also evaluated.

  14. Separation of Quercentin by Pre-dispersed Solvent Extraction

    Institute of Scientific and Technical Information of China (English)

    胡伟; 孙瑛; 叶汝强; 吴树森; 刘洪来

    2003-01-01

    Pre-dispersed solvent extraction (PDSE) was used to extract quercentin from its diluted solution. The influences of temperature, phase volume ratio (PVR), concentration of sodium Dodecyl benzene sulphonate and pH value etc. on the extraction efficiency were examined. It is found that, compared with traditional extraction techniques under the same condition, a higher extraction productivity can be obtained by PDSE. The stability of colloidal liquid aphrons plays an important role in this process. In a certain scope, the extraction efficiency increases with PVR. Excessive amount of solvent is not much helpful. A new analytical method by using ultraviolet spectrometer to determine the concentration of quercentin is established.

  15. Caustic-Side Solvent Extraction: Chemical and Physical Properties of the Optimized Solvent

    Energy Technology Data Exchange (ETDEWEB)

    Delmau, L.H.

    2002-10-08

    This work was undertaken to optimize the solvent used in the Caustic Side Solvent Extraction (CSSX) process and to measure key chemical and physical properties related to its performance in the removal of cesium from the alkaline high-level salt waste stored in tanks at the Savannah River Site. The need to adjust the solvent composition arose from the prior discovery that the previous baseline solvent was supersaturated with respect to the calixarene extractant. The following solvent-component concentrations in Isopar{reg_sign} L diluent are recommended: 0.007 M calix[4]arene-bis(tert-octylbenzo-crown-6) (BOBCalixC6) extractant, 0.75 M 1-(2,2,3,3-tetrafluoropropoxy)-3-(4-sec-butylphenoxy)-2-propanol (Cs-7SB) phase modifier, and 0.003 M tri-n-octylamine (TOA) stripping aid. Criteria for this selection included BOBCalixC6 solubility, batch cesium distribution ratios (D{sub Cs}), calculated flowsheet robustness, third-phase formation, coalescence rate (dispersion numbers), and solvent density. Although minor compromises within acceptable limits were made in flowsheet robustness and solvent density, significant benefits were gained in lower risk of third-phase formation and lower solvent cost. Data are also reported for the optimized solvent regarding the temperature dependence of D{sub Cs} in extraction, scrubbing, and stripping (ESS); ESS performance on recycle; partitioning of BOBCalixC6, Cs-7SB, and TOA to aqueous process solutions; partitioning of organic anions; distribution of metals; solvent phase separation at low temperatures; solvent stability to elevated temperatures; and solvent density and viscosity. Overall, the technical risk of the CSSX process has been reduced by resolving previously identified issues and raising no new issues.

  16. Extraction, scrub, and strip test results for the salt waste processing facility caustic side solvent extraction solvent example

    Energy Technology Data Exchange (ETDEWEB)

    Peters, T. B. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2017-08-01

    An Extraction, Scrub, and Strip (ESS) test was performed on a sample of Salt Waste Processing Facility (SWPF) Caustic-Side Solvent Extraction (CSSX) solvent and salt simulant to determine cesium distribution ratios (D(Cs)), and cesium concentration in the strip effluent (SE) and decontaminated salt solution (DSS) streams; this data will be used by Parsons to help determine if the solvent is qualified for use at the SWPF. The ESS test showed acceptable performance of the solvent for extraction, scrub, and strip operations. The extraction D(Cs) measured 12.9, exceeding the required value of 8. This value is consistent with results from previous ESS tests using similar solvent formulations. Similarly, scrub and strip cesium distribution ratios fell within acceptable ranges.

  17. Removal of Phenol from Dilute Solutions by Predispersed Solvent Extraction

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Predispersed solvent extraction (PDSE) is a new method for separating solutes from aqueous solution by solvent extraction and one which has shown promise for extraction from extremely dilute solution very efficient and very quick. The use of colloidal liquid aphrons in predispersed solvent extraction may ameliorate the problems such as emulsion formation, reduction of interfacial mass transfer and low interfacial mass transfer areas in solvent extraction process. In present paper, colloidal liquid aphrons are successfully generated using kerosene as a solvent, tributyl phosphate(TBP) as an extractant, sodium dodecyl benzene sulphate(SDBS) as surfactant in aqueous phase and Tween-80 in oil phase. Extraction of phenol from dilute solution was studied by using colloidal liquid aphrons and colloidal gas aphrons in a semi-batch extraction column. It has been found that the PDSE process is more suitable for extraction of dilute solutions. It has also been discovered that the PDSE process has a great advantage over traditional single-stage extraction process.

  18. Effective lipid extraction from algae cultures using switchable solvents

    NARCIS (Netherlands)

    Samori, Chiara; Lopez Barreiro, Diego; Vet, Robin; Pezzolesi, Laura; Brilman, Derk W.F. (Wim); Galletti, Paola; Tagliavini, Emilio

    2013-01-01

    A new procedure based on switchable polarity solvents (SPS) was proposed for lipid extraction of wet algal samples or cultures, thereby circumventing the need for an energy intensive drying step and facilitating easy recovery of the lipids from the extraction liquid. Lipids were extracted by using N

  19. Effective lipid extraction from algae cultures using switchable solvents

    NARCIS (Netherlands)

    Samori, Chiara; Lopez Barreiro, D.; Vet, Robin; Pezzolesi, Laura; Brilman, Derk Willem Frederik; Galletti, Paola; Tagliavini, Emilio

    2013-01-01

    A new procedure based on switchable polarity solvents (SPS) was proposed for lipid extraction of wet algal samples or cultures, thereby circumventing the need for an energy intensive drying step and facilitating easy recovery of the lipids from the extraction liquid. Lipids were extracted by using

  20. Comparison of solvent mixtures for pressurized solvent extraction of soil fatty acid biomarkers.

    Science.gov (United States)

    Jeannotte, Richard; Hamel, Chantal; Jabaji, Suha; Whalen, Joann K

    2008-10-19

    The extraction and transesterification of soil lipids into fatty acid methyl esters (FAMEs) is a useful technique for studying soil microbial communities. The objective of this study was to find the best solvent mixture to extract soil lipids with a pressurized solvent extractor system. Four solvent mixtures were selected for testing: chloroform:methanol:phosphate buffer (1:2:0.8, v/v/v), chloroform:methanol (1:2, v/v), hexane:2-propanol (3:2, v/v) and acetone. Soils were from agricultural fields and had a wide range of clay, organic matter and microbial biomass contents. Total lipid fatty acid methyl esters (TL-FAMEs) were the extractable soil lipids identified and quantified with gas chromatography and flame ionization detection. Concentrations of TL-FAMEs ranged from 57.3 to 542.2 nmole g(-1) soil (dry weight basis). The highest concentrations of TL-FAMEs were extracted with chloroform:methanol:buffer or chloroform:methanol mixtures than with the hexane:2-propanol or acetone solvents. The concentrations of TL-FAMEs in chemical groups, including saturated, branched, mono- and poly-unsaturated and hydroxy fatty acids were assessed, and biological groups (soil bacteria, mycorrhizal fungi, saprophytic fungi and higher plants) was distinguished. The extraction efficiency for the chemical and biological groups followed the general trend of: chloroform:methanol:buffer> or =chloroform:methanol>hexane:2-propanol=acetone. Discriminant analysis revealed differences in TL-FAME profiles based on the solvent mixture and the soil type. Although solvent mixtures containing chloroform and methanol were the most efficient for extracting lipids from the agricultural soils in this study, soil properties and the lipid groups to be studied should be considered when selecting a solvent mixture. According to our knowledge, this is the first report of soil lipid extraction with hexane:2-propanol or acetone in a pressurized solvent extraction system.

  1. Next Generation Solvent Performance in the Modular Caustic Side Solvent Extraction Process - 15495

    Energy Technology Data Exchange (ETDEWEB)

    Smith, Tara E. [Savannah River Remediation, LLC., Aiken, SC (United States); Scherman, Carl [Savannah River Remediation, LLC., Aiken, SC (United States); Martin, David [Savannah River Remediation, LLC., Aiken, SC (United States); Suggs, Patricia [Savannah River Site (SRS), Aiken, SC (United States)

    2015-01-14

    Changes to the Modular Caustic Side Solvent Extraction Unit (MCU) flow-sheet were implemented in the facility. Implementation included changing the scrub and strip chemicals and concentrations, modifying the O/A ratios for the strip, scrub, and extraction contactor banks, and blending the current BoBCalixC6 extractant-based solvent in MCU with clean MaxCalix extractant-based solvent. During the successful demonstration period, the MCU process was subject to rigorous oversight to ensure hydraulic stability and chemical/radionuclide analysis of the key process tanks (caustic wash tank, solvent hold tank, strip effluent hold tank, and decontaminated salt solution hold tank) to evaluate solvent carryover to downstream facilities and the effectiveness of cesium removal from the liquid salt waste. Results indicated the extraction of cesium was significantly more effective with an average Decontamination Factor (DF) of 1,129 (range was 107 to 1,824) and that stripping was effective. The contactor hydraulic performance was stable and satisfactory, as indicated by contactor vibration, contactor rotational speed, and flow stability; all of which remained at or near target values. Furthermore, the Solvent Hold Tank (SHT) level and specific gravity was as expected, indicating that solvent integrity and organic hydraulic stability were maintained. The coalescer performances were in the range of processing results under the BOBCalixC6 flow sheet, indicating negligible adverse impact of NGS deployment. After the Demonstration period, MCU began processing via routine operations. Results to date reiterate the enhanced cesium extraction and stripping capability of the Next Generation Solvent (NGS) flow sheet. This paper presents process performance results of the NGS Demonstration and continued operations of MCU utilizing the blended BobCalixC6-MaxCalix solvent under the NGS flowsheet.

  2. 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.

  3. Antimicrobial activity of ultrasound-assisted solvent-extracted spices.

    Science.gov (United States)

    Thongson, C; Davidson, P M; Mahakarnchanakul, W; Weiss, J

    2004-01-01

    The objective of this research was to determine the antimicrobial activity of conventional and high-intensity ultrasound-assisted (HI-US) solvent-extracted Thai spices, including ginger (Zingiber officinale Rose), fingerroot (Bosenbergia pandurata Holtt) and turmeric (Curouma longa Linn). Extracts were obtained using hexane, isopropanol and a 7 : 3 isopropanol : hexane mixture as solvents with and without HI-US. The antimicrobial activity of the extracts was assayed against four strains each of Listeria monocytogenes and Salmonella Typhimurium DT 104 using an agar dilution assay. Application of HI-US did not alter antibacterial activity against S. Typhimurium, but antilisterial activity of some HI-US spice extracts decreased. Solvent type affected antimicrobial efficacy of extracts with hexane producing the least antimicrobial activity. Fingerroot extracted with isopropanol-hexane and without HI-US had the best antilisterial effect while HI-US-isopropanol fingerroot extract had the greatest antimicrobial efficacy against S. Typhimurium. Application of HI-US reduced time of extraction to 5 min, compared with the 24 h required for conventional extraction and maintained antimicrobial activity against Salmonella but slightly reduced activity against Listeria. HI-US in combination with proper solvent selection may offer a new tool to optimize extraction of spice essential oil for use as antimicrobial agents, and reduce processing time and costs.

  4. Carotenoid extraction from plants using a novel, environmentally friendly solvent.

    Science.gov (United States)

    Ishida, Betty K; Chapman, Mary H

    2009-02-11

    Few environmentally friendly solvents are available to extract carotenoids for use in foods. The most effective known solvents are products of the petroleum industry and toxic for human consumption. Yet carotenoid extracts are desirable for use in dietary supplements and as additives to enhance the health benefits of processed foods. Ethyl lactate is an excellent solvent to extract both trans- and cis-lycopene isomers from dried tomato powder, the extraction efficiency of which is enhanced by the addition of the antioxidants alpha-tocopherol and alpha-lipoic acid, both of which are known to benefit human health. It is also useful to extract lutein and beta-carotene from dried powders prepared from white corn and carrots. Because of its low flammability and its origin as a byproduct of the corn and soybean industries, it is more advantageous than ethyl acetate, which is a petroleum product.

  5. Kinetics study of oil extraction from Citrus auranticum L. by solvent-free microwave extraction

    OpenAIRE

    Heri Septya Kusuma; Prilia Dwi Amelia; Cininta Admiralia; Mahfud Mahfud

    2016-01-01

    Citrus and its oil are of high economic and medicinal value because of their multiple uses, such as in the food industry, cosmetics and folk medicine. The aim of this study is to investigate the potential of solvent-free microwave extraction for the extraction of essential oils from Citrus auranticum L. peels. Specifically, this study verifies the kinetics based on second-order model and mechanism of solvent-free microwave extraction of Citrus auranticum L. peels. Solvent-free microwave extra...

  6. Characterization of solvents containing CyMe4-BTPhen in selected cyclohexanone-based diluents after irradiation by accelerated electrons

    Directory of Open Access Journals (Sweden)

    Distler Petr

    2015-12-01

    Full Text Available Radiation stability of CyMe4-BTPhen was examined in systems with three selected cyclohexanone-based diluents. Accelerated electrons were used as a source of ionizing radiation. The CyMe4-BTPhen radiation degradation identification and characterization of the degradation products were performed by high performance liquid chromatography (HPLC and mass spectrometry (MS analyses. Residual concentrations of tested ligand were determined. Moreover, extraction properties of the solvents irradiated at two different doses were compared with the extraction properties of non-irradiated solvents to estimate the influence of the presence of degradation products in the organic phase.

  7. Compound forming extractants, solvating solvents and inert solvents IUPAC chemical data series

    CERN Document Server

    Marcus, Y; Kertes, A S

    2013-01-01

    Equilibrium Constants of Liquid-Liquid Distribution Reactions, Part III: Compound Forming Extractants, Solvating Solvents, and Inert Solvents focuses on the compilation of equilibrium constants of various compounds, such as acids, ions, salts, and aqueous solutions. The manuscript presents tables that show the distribution reactions of carboxylic and sulfonic acid extractants and their dimerization and other reactions in the organic phase and extraction reactions of metal ions from aqueous solutions. The book also states that the inorganic anions in these solutions are irrelevant, since they d

  8. CHEMICAL STABILITY OF POLYPHENYLENE SULFIDE IN THE NEXT GENERATION SOLVENT FOR CAUSTIC-SIDE SOLVENT EXTRACTION

    Energy Technology Data Exchange (ETDEWEB)

    Fondeur, F.; Fink, S.

    2011-12-08

    The Office of Waste Processing, within the Office of Technology Innovation and Development, is funding the development of an enhanced solvent for deployment at the Savannah River Site for removal of cesium from High Level Waste. For simplicity, this solvent is referred to as the Next Generation Solvent (NGS). The technical effort is collaboration between Oak Ridge National Laboratory (ORNL), Savannah River National Laboratory (SRNL), and Argonne National Laboratory. The initial deployment target envisioned for the technology was within the Modular Caustic-Side Solvent Extraction Unit (MCU). Deployment of a new chemical within an existing facility requires verification that the chemical components are compatible with the installed equipment. In the instance of a new organic solvent, the primary focus is on compatibility of the solvent with polyphenylene sulfide (PPS), the polymer used in the coalescers within MCU. This report provides the data from exposing PPS polymer to NGS. The test was conducted over a three month period. PPS is remarkably stable in the presence of the next generation solvent. Testing showed no indication of swelling or significant leaching. Preferential sorption of the Modifier on PPS was observed but the same behavior occurs with the baseline solvent. Therefore, PPS coalescers exposed to the NGS are expected to perform comparably to those in contact with the baseline solvent.

  9. CHEMICAL STABILITY OF POLYPHENYLENE SULFIDE IN THE NEXT GENERATION SOLVENT FOR CAUSTIC-SIDE SOLVENT EXTRACTION

    Energy Technology Data Exchange (ETDEWEB)

    Fondeur, F.; Fink, S.

    2011-12-08

    The Office of Waste Processing, within the Office of Technology Innovation and Development, is funding the development of an enhanced solvent for deployment at the Savannah River Site for removal of cesium from High Level Waste. For simplicity, this solvent is referred to as the Next Generation Solvent (NGS). The technical effort is collaboration between Oak Ridge National Laboratory (ORNL), Savannah River National Laboratory (SRNL), and Argonne National Laboratory. The initial deployment target envisioned for the technology was within the Modular Caustic-Side Solvent Extraction Unit (MCU). Deployment of a new chemical within an existing facility requires verification that the chemical components are compatible with the installed equipment. In the instance of a new organic solvent, the primary focus is on compatibility of the solvent with polyphenylene sulfide (PPS), the polymer used in the coalescers within MCU. This report provides the data from exposing PPS polymer to NGS. The test was conducted over a three month period. PPS is remarkably stable in the presence of the next generation solvent. Testing showed no indication of swelling or significant leaching. Preferential sorption of the Modifier on PPS was observed but the same behavior occurs with the baseline solvent. Therefore, PPS coalescers exposed to the NGS are expected to perform comparably to those in contact with the baseline solvent.

  10. Antimicrobial potentials of different solvent extracted samples from Physalis ixocarpa.

    Science.gov (United States)

    Khan, Wajid; Bakht, Jehan; Shafi, Mohammad

    2016-03-01

    The present study investigates the antimicrobial activities of different solvent extracted samples isolated from different parts of Physalis ixocarpa through disc diffusion assay using three different concentrations. Statistical analysis of the data revealed that different parts of the plant showed varying degree of inhibition against different bacteria at different concentrations. Different solvent extracted samples from the calyx showed inhibitory activity against most of the bacteria under study. Extracts from leaf and fruit samples showed activity against S. aureus and K. pneumoniae and extracts from the stem tissues were effective to control the growth of E. coli and K. pneumoniae. Crude methanolic extract from the stem and n-butanol extracted samples from fruit exhibited strong inhibitory activity against Klebsiella pneumoniae at highest concentrations. Antifungal activity was observed only in crude methanol extract from the leaf against Rhizopus stolinifer, Aspergillus niger and Penicillium chrysogenum.

  11. Interfacial chemistry in solvent extraction systems

    Energy Technology Data Exchange (ETDEWEB)

    Neuman, R.D.

    1993-01-01

    Research this past year continued to emphasize characterization of the physicochemical nature of the microscopic interfaces, i.e., reversed micelles and other association microstructures, which form in both practical and simplified acidic organophosphorus extraction systems associated with Ni, Co, and Na in order to improve on the model for aggregation of metal-extractant complexes. Also, the macroscopic interfacial behavior of model extractant (surfactant) molecules was further investigated. 1 fig.

  12. COBALT SALTS PRODUCTION BY USING SOLVENT EXTRACTION

    OpenAIRE

    Liudmila V. Dyakova; Aleksander G. Kasikov; Elena S. Kshumaneva; Svetlana V. Drogobuzhskaya

    2010-01-01

    The paper deals with the extracting cobalt salts by using mixtures on the basis of tertiary amine from multicomponent solutions from the process of hydrochloride leaching of cobalt concentrate. The optimal composition for the extraction mixture, the relationship between the cobalt distribution coefficients and modifier’s nature and concentration, and the saltingout agent type have been determined. A hydrochloride extraction technology of cobalt concentrate yielding a purified concentrated cob...

  13. Solvent extraction of gold using ionic liquid based process

    Science.gov (United States)

    Makertihartha, I. G. B. N.; Zunita, Megawati; Rizki, Z.; Dharmawijaya, P. T.

    2017-01-01

    In decades, many research and mineral processing industries are using solvent extraction technology for metal ions separation. Solvent extraction technique has been used for the purification of precious metals such as Au and Pd, and base metals such as Cu, Zn and Cd. This process uses organic compounds as solvent. Organic solvents have some undesired properties i.e. toxic, volatile, excessive used, flammable, difficult to recycle, low reusability, low Au recovery, together with the problems related to the disposal of spent extractants and diluents, even the costs associated with these processes are relatively expensive. Therefore, a lot of research have boosted into the development of safe and environmentally friendly process for Au separation. Ionic liquids (ILs) are the potential alternative for gold extraction because they possess several desirable properties, such as a the ability to expanse temperature process up to 300°C, good solvent properties for a wide range of metal ions, high selectivity, low vapor pressures, stability up to 200°C, easy preparation, environmentally friendly (commonly called as "green solvent"), and relatively low cost. This review paper is focused in investigate of some ILs that have the potentials as solvent in extraction of Au from mineral/metal alloy at various conditions (pH, temperature, and pressure). Performances of ILs extraction of Au are studied in depth, i.e. structural relationship of ILs with capability to separate Au from metal ions aggregate. Optimal extraction conditon in order to gain high percent of Au in mineral processing is also investigated.

  14. Solvent-free extraction of food and natural products

    OpenAIRE

    Fabiano-Tixier, Anne-Sylvie; Vian, Maryline; Allaf, Tamara; Vorobiev, Eugene

    2015-01-01

    This review presents useful and green techniques of solvent-free extraction used in ancient times, such as extraction of olive oil and citrus essential oil, and innovative techniques, such as pulsed electric field, microwave, instantaneous controlled pressure drop, and extrusion. We discuss the devices, their applications, mechanisms, and parameters influencing sample preparation prior to analysis of natural products.

  15. A new model for solvent extraction in columns

    Energy Technology Data Exchange (ETDEWEB)

    Leonard, R.A.; Regalbuto, M.C.; Chamberlain, D.B.; Vandegrift, G.F.

    1989-12-08

    A new model was developed for analyzing solvent extraction processes carried out in columns. Each column is treated as a series of well-defined equilibrium stages where the backmixing (other-phase carryover) between stages can be large. By including all mass transfer effects in the backmixing value, the same number of stages can be used for all extracted components no matter what their distribution coefficients. This greatly simplifies the calculations required when modeling multicomponent solvent extraction processes. Initial testing shows the new model to be better than either the Height of an Equivalent Theoretical Plate (HETP) or the Height of a Transfer Unit (HTU) method.

  16. Mechanism of crud formation in copper solvent extraction

    Institute of Scientific and Technical Information of China (English)

    柳建设; 蓝卓越; 邱冠周; 王淀佐

    2002-01-01

    The authors investigated the mechanism of crud formation in copper solvent extraction. It is indicated that pH value of solution and the phase ratio (O/A) are the main factors affecting crud formation in solvent extraction. The amount of crud extraction increases with aqueous pH value increase, and reduces with the increase of the phase ratio. Fe3+, Mg2+, fine air bubble and suspended particulates in leaching solution contribute to crud formation. One case is that a series of reactions of hydrolization and polymerization occurs for Fe3+, while pH>2.5, polyhydric complex or Fe-SO4 complex are formed. Then the complex-ions of FeOH2+, Fe2(OH)4+2 cause poly-reaction, which is likely to lead emulsion. The study on Zeta potential indicates the repulsion between electriferous droplets in solvent extraction prevents phase coalescence, which is one of the major reasons for emulsion.

  17. Ultrasound Energy Effect on Solvent Extraction of Amaranth Seed Oil

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Won Il; Chung, Ki Won; Lee, Seung Bum; Hong, In Kwon [Department of Chemical Engineering, Dankook University, Seoul (Korea); Park, Kyung Ai [Seoul Metropolitan Government Institute of Health and Environment, Seoul (Korea)

    2001-05-01

    Ultrasonic energy has been widely applied to cleaning, medical appliances, extraction, etc. And ultrasonic energy can be applied to solvent extraction of plant oil from amaranth seed. Amaranth seed oil contains small amount of squalene. Squalene is polyunsaturated branched hydrocarbon, which is an essential part of the human body. In this study, the seed oil was extracted from amaranth seed by ultrasonic solvent extraction process. Ultrasonic irradiation time was 1, 3 ,5, 10, 20 and 30 min and extraction temperature was 20, 30, and 40 degree C. And ultrasonic power was 390 W and 520 W. The extracted amounts of amaranth seed oil and squalene were increased with the increase of ultrasonic power and irradiation time. Using ultrasonic energy in solvent extraction, extraction time was very shorten. The optimum extraction temperature was 30 degree C, it was caused that ultrasonic energy effects were increased in the matters of low temperature. The maximum extracted amount of amaranth seed oil was 0.746 g and squalene was 37.54 mg per 10 g amaranth seed at 30 degree C. 10 refs., 8 figs., 1 tab.

  18. COBALT SALTS PRODUCTION BY USING SOLVENT EXTRACTION

    Directory of Open Access Journals (Sweden)

    Liudmila V. Dyakova

    2010-06-01

    Full Text Available The paper deals with the extracting cobalt salts by using mixtures on the basis of tertiary amine from multicomponent solutions from the process of hydrochloride leaching of cobalt concentrate. The optimal composition for the extraction mixture, the relationship between the cobalt distribution coefficients and modifier’s nature and concentration, and the saltingout agent type have been determined. A hydrochloride extraction technology of cobalt concentrate yielding a purified concentrated cobalt solution for the production of pure cobalt salts has been developed and introduced at Severonikel combine.

  19. Oil recovery from petroleum sludge through ultrasonic assisted solvent extraction.

    Science.gov (United States)

    Hu, Guangji; Li, Jianbing; Huang, Shuhui; Li, Yubao

    2016-09-18

    The effect of ultrasonic assisted extraction (UAE) process on oil recovery from refinery oily sludge was examined in this study. Two types of UAE treatment including UAE probe (UAEP) system and UAE bath (UAEB) system were investigated. Their oil recovery efficiencies were compared to that of mechanical shaking extraction (MSE). Three solvents including cyclohexane (CHX), ethyl acetate (EA), and methyl ethyl ketone (MEK) were examined as the extraction solvents. The influence of experimental factors on oil and solvent recovery was investigated using an orthogonal experimental design. Results indicated that solvent type, solvent-to-sludge (S/S) ratio, and treatment duration could have significant effects on oil recovery in UAE treatment. Under the optimum conditions, UAEP treatment can obtain an oil recovery of 68.8% within 20 s, which was higher than that (i.e., 62.0%) by MSE treatment after 60 min' extraction. UAEB treatment can also obtain a promising oil recovery within shorter extraction duration (i.e., 15 min) than MSE. UAE was thus illustrated as an effective and improved approach for oily sludge recycling.

  20. SPIRAL CONTACTOR FOR SOLVENT EXTRACTION COLUMN

    Science.gov (United States)

    Cooley, C.R.

    1961-06-13

    The patented extraction apparatus includes a column, perforated plates extending across the column, liquid pulse means connected to the column, and an imperforate spiral ribbon along the length of the column.

  1. SOLVENT EXTRACTION FOR URANIUM MOLYBDENUM ALLOY DISSOLUTION FLOWSHEET

    Energy Technology Data Exchange (ETDEWEB)

    Visser, A; Robert Pierce, R

    2007-06-07

    H-Canyon Engineering requested the Savannah River National Laboratory (SRNL) to perform two solvent extraction experiments using dissolved Super Kukla (SK) material. The SK material is an uranium (U)-molybdenum (Mo) alloy material of 90% U/10% Mo by weight with 20% 235U enrichment. The first series of solvent extraction tests involved a series of batch distribution coefficient measurements with 7.5 vol % tributylphosphate (TBP)/n-paraffin for extraction from 4-5 M nitric acid (HNO{sub 3}), using 4 M HNO{sub 3}-0.02 M ferrous sulfamate (Fe(SO3NH2)2) scrub, 0.01 M HNO3 strip steps with particular emphasis on the distribution of U and Mo in each step. The second set of solvent extraction tests determined whether the 2.5 wt % sodium carbonate (Na2CO3) solvent wash change frequency would need to be modified for the processing of the SK material. The batch distribution coefficient measurements were performed using dissolved SK material diluted to 20 g/L (U + Mo) in 4 M HNO{sub 3} and 5 M HNO{sub 3}. In these experiments, U had a distribution coefficient greater than 2.5 while at least 99% of the nickel (Ni) and greater than 99.9% of the Mo remained in the aqueous phase. After extraction, scrub, and strip steps, the aqueous U product from the strip contains nominally 7.48 {micro}g Mo/g U, significantly less than the maximum allowable limit of 800 {micro}g Mo/g U. Solvent washing experiments were performed to expose a 2.5 wt % Na2CO3 solvent wash solution to the equivalent of 37 solvent wash cycles. The low Mo batch distribution coefficient in this solvent extraction system yields only 0.001-0.005 g/L Mo extracted to the organic. During the solvent washing experiments, the Mo appears to wash from the organic.

  2. The Solvent Effectiveness on Extraction Process of Seaweed Pigment

    Directory of Open Access Journals (Sweden)

    Warkoyo Warkoyo

    2011-09-01

    Full Text Available Eucheuma cottonii seaweed is a species of seaweed cultured in Indonesian waters, because its cultivation is relatively easy and inexpensive. It has a wide variety of colors from green to yellow green, gray, red and brown, indicating photosynthetic pigments, such as chlorophyll and carotenoids. An important factor in the effectiveness of pigment extraction is the choice of solvent. The correct type of solvent in the extraction method of specific natural materials is important so that a pigment with optimum quality that is also benefical to the society can be produced. The target of this research is to obtain a high quality solvent type of carotenoid pigment. This research was conducted using a randomized block design with three (3 replications involving two factors namely solvent type (4 levels: aceton, ethanol, petroleum benzene, hexan & petroleum benzene and seaweed color (3 levels: brown, green and red. Research results indicated that each solvent reached a peak of maximal absorbance at  410-472 nm, namely carotenoids. The usage of acetone solvent gave the best pigment quality. Brown, green and red seaweed have pigment content of 1,28 mg/100 g; 0,98 mg/100 g; 1,35 mg/100 g and rendement of 6,24%; 4,85% and 6,65% respectively.

  3. Deacidification of Soybean Oil Combining Solvent Extraction and Membrane Technology

    Directory of Open Access Journals (Sweden)

    M. L. Fornasero

    2013-01-01

    Full Text Available The aim of this work was to study the removal of free fatty acids (FFAs from soybean oil, combining solvent extraction (liquid-liquid for the separation of FFAs from the oil and membrane technology to recover the solvent through nanofiltration (NF. Degummed soybean oil containing 1.05 ± 0.10% w/w FFAs was deacidified by extraction with ethanol. Results obtained in the experiences of FFAs extraction from oil show that the optimal operating conditions are the following: 1.8 : 1 w : w ethanol/oil ratio, 30 minutes extraction time and high speed of agitation and 30 minutes repose time after extraction at ambient temperature. As a result of these operations two phases are obtained: deacidified oil phase and ethanol phase (containing the FFAs. The oil from the first extraction is subjected to a second extraction under the same conditions, reducing the FFA concentration in oil to 0.09%. Solvent recovery from the ethanol phase is performed using nanofiltration technology with a commercially available polymeric NF membrane (NF-99-HF, Alfa Laval. From the analysis of the results we can conclude that the optimal operating conditions are pressure of 20 bar and temperature of 35°C, allowing better separation performance: permeate flux of 28.3 L/m2·h and FFA retention of 70%.

  4. 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.

  5. Rare earth element enrichment using membrane based solvent extraction

    Science.gov (United States)

    Makertiharta, I. G. B. N.; Dharmawijaya, P. T.; Zunita, M.; Wenten, I. G.

    2017-01-01

    The chemical, catalytic, electrical, magnetic, and optical properties of rare earth elements are required in broad applications. Rare earth elements have similar physical and chemical properties thus it is difficult to separate one from each other. Rare earth element is relatively abundant in earth's crust but rarely occur in high concentrated deposits. Traditionally, ion-exchange and solvent extraction techniques have been developed to separate and purify single rare earth solutions or compounds. Recently, membrane starts to gain attention for rare earth separation by combining membrane and proven technologies such as solvent extraction. Membrane-based process offers selective, reliable, energy efficient and easy to scale up separation. During membrane-based separation process, one phase passes through membrane pores while the other phase is rejected. There is no direct mixing of two phases thus the solvent loss is very low. Membrane can also lower solvent physical properties requirement (viscosity, density) and backmixing, eliminate flooding phenomenon and provide large interfacial area for mass transfer. This paper will summarize research efforts in developing membrane technology for rare earth element separation. Special attention will be given to solvent extraction related process as the commonly used method for rare earth element separation. Furthermore, membrane configuration and its potentials will also be discussed.

  6. Kinetics study of oil extraction from Citrus auranticum L. by solvent-free microwave extraction

    Directory of Open Access Journals (Sweden)

    Heri Septya Kusuma

    2016-05-01

    Full Text Available Citrus and its oil are of high economic and medicinal value because of their multiple uses, such as in the food industry, cosmetics and folk medicine. The aim of this study is to investigate the potential of solvent-free microwave extraction for the extraction of essential oils from Citrus auranticum L. peels. Specifically, this study verifies the kinetics based on second-order model and mechanism of solvent-free microwave extraction of Citrus auranticum L. peels. Solvent-free microwave extraction is used to extract essential oils from Citrus auranticum L. peels. The initial extraction rate, the extraction capacity and the second-order extraction rate constant were calculated using the model. Using a three-step experimental design of the kinetics of oil extraction from Citrus auranticum L. peels by solvent-free microwave extraction, this study showed that the extraction process was based on the second-order extraction model. The initial extraction rate (h, the extraction capacity (CS, the second-order extraction rate constant (k, and coefficient of determination (R2 was 0.7483 g L-1 min-1, 0.7291 g L-1, 1.4075 L g-1 min-1 and 0.9992, respectively.

  7. Application of ultrasound in solvent extraction of nickel and gallium

    Energy Technology Data Exchange (ETDEWEB)

    Pesic, B.

    1996-07-01

    The effects of ultrasound on the rate of solvent extraction of nickel with Lix 65N and Lix 70, and gallium with Kelex 100 were investigated. These solvent extraction systems are noted by their sluggish nature. Low frequency (20 kHz) ultrasound increased the rates of extraction of nickel by factors of four to seven. The ultrasound had no effect on the final chemical equilibrium. Gallium extraction rates were enhanced with the use of ultrasound by as much as a factor of 15. Again, the ultrasound had no effect on extraction equilibrium. For both nickel and gallium, the enhanced rates were attributed to increased interfacial surface area associated with ultrasonically induced cavitation and microdroplet formation. The stability of the microdroplets permitted intermittent application of ultrasound with corresponding decreases in ultrasonic energy requirements. The lowest energy consumption was observed with short (0.25 to 5 s) bursts of high power (41 to 61 W) ultrasonic inputs. The study also provided insight into the factors that affect the complex extraction of gallium from sodium aluminate solutions. The rate controlling step was found to be the dehydration of the gallate ion, Ga(OH)4, and the first complex formation between gallium and Kelex 100. Sodium was found to enhance the extraction rate up to a point, beyond which increased concentration was detrimental. Increasing aluminum concentration was found to slow extraction rates. Modifiers and diluents were shown to markedly affect extraction rates even without ultrasound. Ketone modifiers, particularly 2-undecanone, when used with Kermac 470B or Escaid 200 diluents enhanced extraction rates of gallium to the point that the use of ultrasound provided no additional benefits. The positive effects of ketone modifiers for the solvent extraction of gallium had not been previously reported.

  8. 加速溶剂萃取-固相萃取-液相色谱-电喷雾串联质谱法同时测定羊栖菜中六溴环十二烷异构体%Simultaneous determination of hexabromocyclododecane diastereoisomers in Sargassum fusiforme by accelerated solvent extraction-solid phase extraction-liquid chromatography-tandem mass spectrometry

    Institute of Scientific and Technical Information of China (English)

    韩超; 贾婉娉; 朱振瓯; 刘滨; 刘翠平; 沈燕

    2011-01-01

    采用同位素稀释-高效液相色谱-电喷雾串联四级杆质谱法同时测定羊栖菜中3种六溴环十二烷(HBCD)非对映异构体.羊栖菜样品磨碎、加入同位素内标13C-HBCD后以乙酸乙酯为提取溶剂,采用加速溶剂萃取法,使用Waters X Bridge(TM)C18反相柱分离;流动相为10mmoL的乙酸铵/乙腈(0.1%乙酸)/甲醇,在等度条件下分析,目标分析物在多反应监测(MRM)模式下以保留时间和离子对(母离子和两个碎片离子)信息比较进行定性分析,内标法定量.结果表明,在7min内即可完成α,β和γ-HBCD 3种同分异构体的分离,检测限(LOD)为0.3~1.0ng/g,定量限(LOQ)为1.0~4.0ng/g,添加水平为5、10和25ng/g时,3种被测物的加标回收率为92.7%~102.5%,相对标准偏差小于3.9%.本方法为评价羊栖菜样品质量提供了新的检测方法.%A method for the detection of α, β and γ-diastereoisomers of hexabrom ocyclododecanes (HBCDs) in Sargassum Fusiforme was developed using liquid chromatography-electrospray inonization mass spectrometry and isotope dilution. The samples were ground、added isotopic internal standard13C-HBCD and then extracted under the conditions of 10. 3 MPa and 80 ℃ by accelerated solvent extraction method with two static cycles using ethyl acetate as the extraction solvent. The extract was cleaned up by solid phase extraction cartridge. The analysis was performed on an Waters X BridgeTM C18 column(2.1 x 150 mm,3.5 μm) utilizing a isocratic elution profile and a mobile phase of water with 10 mmol/L ammonium acetate/acetonitrile with O. 1% acetic acid/ methanol.The analytes were detected using an electro-spray ionization tandem mass spectrometry with multiple reaction monitoring. Qualitative and quantitative analysis was based on the peak area of the parent ion and two fragment ions, and quantified by internal standard method. The results showed that the three HBCDs were separated within 7 min. The instrumental limits of

  9. Juniperus extraction: a comparison of species and solvents

    Science.gov (United States)

    The effectiveness of the three solvents, hexane, methanol and ethanol were compared for their ability to extract non-polar and polar materials from sawdust from three species of Juniperus (i.e., J. virginianna, J. occidentalis and J. ashei). These species studied represent the junipers with the grea...

  10. Fuel grade ethanol by solvent extraction: Final subcontract report

    Energy Technology Data Exchange (ETDEWEB)

    Tedder, D.W.

    1987-04-01

    This report summarizes final results for ethanol recovery by solvent extraction and extractive distillation. At conclusion this work can be summarized as ethanol dehydration and recovery dilute fermentates is feasible using liquid/liquid extraction and extractive distillation. Compared to distillation, the economics are more attractive for less than 5 wt % ethanol. However, an economic bias in favor of SEED appears to exist even for 10 wt % feeds. It is of particular interest to consider the group extraction of ethanol and acetic acid followed by conversion to a mixture of ethanol and ethyl acetate. The latter species is a more valuable commodity and group extraction of inhibitory species is one feature of liquid/liquid extraction that is not easily accomodated using distillation. Upflow immobilized reactors offer the possibility of achieving high substrate conversion while also maintaining low metabolite concentrations. However, many questions remain to be answered with such a concept. 135 refs., 42 figs., 61 tabs.

  11. Stability of the Caustic-Side Solvent Extraction (CSSX) Process Solvent: Effect of High Nitrite on Solvent Nitration

    Energy Technology Data Exchange (ETDEWEB)

    Bonnesen, P.V.

    2002-06-26

    The purpose of this investigation was to determine whether nitrated organic compounds could be formed during operation of the Caustic-Side Solvent Extraction (CSSX) process, and whether such compounds would present a safety concern. The CSSX process was developed to remove cesium from alkaline high-level salt waste stored at the US Department of Energy Savannah River Site (SRS). The solvent is composed of the cesium extractant calix[4]arene-bis-(4-tert-octylbenzo-crown-6) (BOBCalixC6), a fluorinated alcohol phase modifier, tri-n-octylamine (TOA), and an isoparaffinic diluent (Iospar{reg_sign}). During the CSSX process, the solvent is expected to be exposed to high concentrations of nitrate and nitrite dissolved in the alkaline waste feed. The solvent will also be exposed to dilute (50 mM) nitric acid solutions containing low concentrations of nitrite during scrubbing, followed by stripping with 1 mM nitric acid. The solvent is expected to last for one year of plant operation, and the temperatures the solvent may experience during the process could range from as low as 15 C to as high as 35 C. Excursions from standard process conditions could result in the solvent experiencing higher temperatures, as well as concentrations of nitrate, nitrite, and most importantly nitric acid, that exceed normal operating conditions. Accordingly, conditions may exist where nitration reactions involving the solvent components, possibly leading to other chemical reactions stemming from nitration reactions, could occur. To model such nitration reactions, the solvent was exposed to the types of nitrate- and nitrite-containing solutions that might be expected to be encountered during the process (even under off-normal conditions), as a function of time, temperature, and concentration of nitrate, nitrite, and nitric acid. The experiments conducted as part of this report were designed to examine the more specific effect that high nitrite concentrations could have on forming nitrated

  12. Development of Solvent Extraction Approach to Recycle Enriched Molybdenum Material

    Energy Technology Data Exchange (ETDEWEB)

    Tkac, Peter [Argonne National Lab. (ANL), Argonne, IL (United States). Nuclear Engineering Division; Brown, M. Alex [Argonne National Lab. (ANL), Argonne, IL (United States). Nuclear Engineering Division; Sen, Sujat [Argonne National Lab. (ANL), Argonne, IL (United States). Energy Systems Division; Bowers, Delbert L. [Argonne National Lab. (ANL), Argonne, IL (United States). Nuclear Engineering Division; Wardle, Kent [Argonne National Lab. (ANL), Argonne, IL (United States). Nuclear Engineering Division; Copple, Jacqueline M. [Argonne National Lab. (ANL), Argonne, IL (United States). Nuclear Engineering Division; Pupek, Krzysztof Z. [Argonne National Lab. (ANL), Argonne, IL (United States). Nuclear Engineering Division; Dzwiniel, Trevor L. [Argonne National Lab. (ANL), Argonne, IL (United States). Energy Systems Division; Pereira, Candido [Argonne National Lab. (ANL), Argonne, IL (United States). Nuclear Engineering Division; Krumdick, Gregory K. [Argonne National Lab. (ANL), Argonne, IL (United States). Energy Systems Division; Vandegrift, George F. [Argonne National Lab. (ANL), Argonne, IL (United States). Nuclear Engineering Division

    2016-06-01

    Argonne National Laboratory, in cooperation with Oak Ridge National Laboratory and NorthStar Medical Technologies, LLC, is developing a recycling process for a solution containing valuable Mo-100 or Mo-98 enriched material. Previously, Argonne had developed a recycle process using a precipitation technique. However, this process is labor intensive and can lead to production of large volumes of highly corrosive waste. This report discusses an alternative process to recover enriched Mo in the form of ammonium heptamolybdate by using solvent extraction. Small-scale experiments determined the optimal conditions for effective extraction of high Mo concentrations. Methods were developed for removal of ammonium chloride from the molybdenum product of the solvent extraction process. In large-scale experiments, very good purification from potassium and other elements was observed with very high recovery yields (~98%).

  13. Microfluidic Extraction of Biomarkers using Water as Solvent

    Science.gov (United States)

    Amashukeli, Xenia; Manohara, Harish; Chattopadhyay, Goutam; Mehdi, Imran

    2009-01-01

    A proposed device, denoted a miniature microfluidic biomarker extractor (mu-EX), would extract trace amounts of chemicals of interest from samples, such as soils and rocks. Traditionally, such extractions are performed on a large scale with hazardous organic solvents; each solvent capable of dissolving only those molecules lying within narrow ranges of specific chemical and physical characteristics that notably include volatility, electric charge, and polarity. In contrast, in the mu-EX, extractions could be performed by use of small amounts (typically between 0.1 and 100 L) of water as a universal solvent. As a rule of thumb, in order to enable solvation and extraction of molecules, it is necessary to use solvents that have polarity sufficiently close to the polarity of the target molecules. The mu-EX would make selection of specific organic solvents unnecessary, because mu-EX would exploit a unique property of liquid water: the possibility of tuning its polarity to match the polarity of organic solvents appropriate for extraction of molecules of interest. The change of the permittivity of water would be achieved by exploiting interactions between the translational states of water molecules and an imposed electromagnetic field in the frequency range of 300 to 600 GHz. On a molecular level, these interactions would result in disruption of the three-dimensional hydrogen-bonding network among liquid-water molecules and subsequent solvation and hydrolysis of target molecules. The mu-EX is expected to be an efficient means of hydrolyzing chemical bonds in complex macromolecules as well and, thus, enabling analysis of the building blocks of these complex chemical systems. The mu-EX device would include a microfluidic channel, part of which would lie within a waveguide coupled to an electronically tuned source of broad-band electromagnetic radiation in the frequency range from 300 to 600 GHz (see figure). The part of the microfluidic channel lying in the waveguide would

  14. Solvent extractants for nickel and cobalt: New opportunities in aqueous processing

    Science.gov (United States)

    Mihaylov, Indje

    2003-07-01

    The last two decades have witnessed unprecedented growth in the development and implementation of solvent extraction technology in the extractive metallurgy of nickel and cobalt. Solvent extraction is proving to be a powerful tool, opening new opportunities for simpler, more cost-efficient and environmentally sound metal refining processes. This article provides an overview of some of the latest developments regarding the solvent extractants.

  15. Next Generation Solvent Development for Caustic-Side Solvent Extraction of Cesium

    Energy Technology Data Exchange (ETDEWEB)

    Moyer, Bruce A. [Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States); Birdwell, Joseph F. [Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States); Bonnesen, Peter V. [Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States); Bruffey, Stephanie [Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)

    2014-03-01

    This report summarizes the FY 2010 and 2011 accomplishments at Oak Ridge National Laboratory (ORNL) in developing the Next Generation Caustic-Side Solvent Extraction (NG-CSSX) process, referred to commonly as the Next Generation Solvent (NGS), under funding from the U.S. Department of Energy, Office of Environmental Management (DOE-EM), Office of Technology Innovation and Development. The primary product of this effort is a process solvent and preliminary flowsheet capable of meeting a target decontamination factor (DF) of 40,000 for worst-case Savannah River Site (SRS) waste with a concentration factor of 15 or higher in the 18-stage equipment configuration of the SRS Modular Caustic-Side Solvent Extraction Unit (MCU). In addition, the NG-CSSX process may be readily adapted for use in the SRS Salt Waste Processing Facility (SWPF) or in supplemental tank-waste treatment at Hanford upon appropriate solvent or flowsheet modifications. Efforts in FY 2010 focused on developing a solvent composition and process flowsheet for MCU implementation. In FY 2011 accomplishments at ORNL involved a wide array of chemical-development activities and testing up through single-stage hydraulic and mass-transfer tests in 5-cm centrifugal contactors. Under subcontract from ORNL, Argonne National Laboratory (ANL) designed a preliminary flowsheet using ORNL cesium distribution data, and Tennessee Technological University confirmed a chemical model for cesium distribution ratios (DCs) as a function of feed composition. Inter laboratory efforts were coordinated with complementary engineering tests carried out (and reported separately) by personnel at Savannah River National Laboratory (SRNL) and Savannah River Remediation (SRR) with helpful advice by Parsons Engineering and General Atomics on aspects of possible SWPF implementation.

  16. Next Generation Solvent (NGS): Development for Caustic-Side Solvent Extraction of Cesium

    Energy Technology Data Exchange (ETDEWEB)

    Moyer, Bruce A. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Birdwell, Jr, Joseph F. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Bonnesen, Peter V. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Bruffey, Stephanie H. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Delmau, Laetitia Helene [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Duncan, Nathan C. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Ensor, Dale [Tennessee Technological Univ., Cookeville, TN (United States); Hill, Talon G. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Lee, Denise L. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Rajbanshi, Arbin [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Roach, Benjamin D. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Szczygiel, Patricia L. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Sloop, Jr., Frederick V. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Stoner, Erica L. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Williams, Neil J. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

    2014-03-01

    This report summarizes the FY 2010 and 2011 accomplishments at Oak Ridge National Laboratory (ORNL) in developing the Next Generation Caustic-Side Solvent Extraction (NG-CSSX) process, referred to commonly as the Next Generation Solvent (NGS), under funding from the U.S. Department of Energy, Office of Environmental Management (DOE-EM), Office of Technology Innovation and Development. The primary product of this effort is a process solvent and preliminary flowsheet capable of meeting a target decontamination factor (DF) of 40,000 for worst-case Savannah River Site (SRS) waste with a concentration factor of 15 or higher in the 18-stage equipment configuration of the SRS Modular Caustic-Side Solvent Extraction Unit (MCU). In addition, the NG-CSSX process may be readily adapted for use in the SRS Salt Waste Processing Facility (SWPF) or in supplemental tank-waste treatment at Hanford upon appropriate solvent or flowsheet modifications. Efforts in FY 2010 focused on developing a solvent composition and process flowsheet for MCU implementation. In FY 2011 accomplishments at ORNL involved a wide array of chemical-development activities and testing up through single-stage hydraulic and mass-transfer tests in 5-cm centrifugal contactors. Under subcontract from ORNL, Argonne National Laboratory (ANL) designed a preliminary flowsheet using ORNL cesium distribution data, and Tennessee Technological University confirmed a chemical model for cesium distribution ratios (DCs) as a function of feed composition. Interlaboratory efforts were coordinated with complementary engineering tests carried out (and reported separately) by personnel at Savannah River National Laboratory (SRNL) and Savannah River Remediation (SRR) with helpful advice by Parsons Engineering and General Atomics on aspects of possible SWPF implementation.

  17. Simultaneous extraction of flavonoids from Chamaecyparis obtusa using deep eutectic solvents as additives of conventional extractions solvents.

    Science.gov (United States)

    Tang, Baokun; Park, Ha Eun; Row, Kyung Ho

    2015-01-01

    Three flavones (quercetin, myricetin and amentoflavone) were extracted from Chamaecyparis obtusa leaves using deep eutectic solvents (DESs) as additives to conventional extractions solvents. Sixteen DESs were synthesized from different salts and hydrogen bond donors. In addition, C. obtusa was extracted under optimal conditions of methanol as the solvent in the heating process (60°C) for 120 min at a solid/liquid ratio of 80%. Under these optimal conditions, a good linear relationship was observed at analyte concentrations ranging from 5.0 to 200.0 μg/mL (R(2) > 0.999). The extraction recovery ranged from 96.7 to 103.3% with the inter- and intraday relative standard deviations of <4.97%. Under the optimal conditions, from C. obtusa, the quantities of quercetin, myricetin and amentoflavone extracted were 325.90, 8.66 and 50.34 µg/mL, respectively. Overall, DESs are expected to have a wide range of applications. © The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

  18. Effect of solvent type and ratio on betacyanins and antioxidant activity of extracts from Hylocereus polyrhizus flesh and peel by supercritical fluid extraction and solvent extraction.

    Science.gov (United States)

    Fathordoobady, Farahnaz; Mirhosseini, Hamed; Selamat, Jinap; Manap, Mohd Yazid Abd

    2016-07-01

    The main objective of the present study was to investigate the effect of solvent type and ratio as well as the extraction techniques (i.e. supercritical fluid extraction (SFE) and conventional solvent extraction) on betacyanins and antioxidant activity of the peel and fresh extract from the red pitaya (Hylocereus polyrhizus). The peel and flesh extracts obtained by SFE at 25MPa pressure and 10% EtOH/water (v/v) mixture as a co-solvent contained 24.58 and 91.27mg/100ml total betacyanin, respectively; while the most desirable solvent extraction process resulted in a relatively higher total betacyanin in the peel and flesh extracts (28.44 and 120.28mg/100ml, respectively). The major betacyanins identified in the pitaya peel and flesh extracts were betanin, isobetanin, phyllocactin, butyrylbetanin, isophyllocactin and iso-butyrylbetanin. The flesh extract had the stronger antioxidant activity than the peel extract when the higher proportion of ethanol to water (E/W) was applied for the extraction.

  19. Solvent extraction of radionuclides from aqueous tank waste

    Energy Technology Data Exchange (ETDEWEB)

    Bonnesen, P.; Sachleben, R.; Moyer, B. [Oak Ridge National Lab., TN (United States)

    1996-10-01

    The purpose of this task is to develop an efficient solvent-extraction and stripping process to remove the fission products {sup 99}Tc, {sup 90}Sr, and {sup 137}Cs from alkaline tank waste, such as those stored at Hanford and Oak Ridge. As such, this task expands on FY 1995`s successful development of a solvent-extraction and stripping process for technetium separation from alkaline tank-waste solutions. This process now includes the capability of removing both technetium and strontium simultaneously. In this form, the process has been named SRTALK and will be developed further in this program as a prelude to developing a system capable of removing technetium, strontium, and cesium.

  20. 快速溶剂萃取–气相色谱质谱法测定土壤中戊唑醇残留量%Determination of Residue Tebuconazole in Soil by Accelerated Solvent Extraction and Gas Chromatography Mass Spectrometry

    Institute of Scientific and Technical Information of China (English)

    吴小春; 姚科伟; 魏双利; 翁际渊; 章巧林; 王鼎

    2015-01-01

    A method was established to determine residue tebuconazole in soil by accelerated solvent extraction and gas chromatography mass spectrometry. Soil sample was prepared byASE–350 fast solvent extraction,purified and concentrated by magnesium silicate (florisil) column. The extract was injected into GC for separation and followed by MS detection under EI ionization and synchronous SIM/SCAN data acquisition mode. The detection limit found for tebuconazole in soil was 0.008 mg/kg,the recovery was 84.0%–97.5%,RSD was 2.2%–11.6%(n=6). The method could be used to detect the residue tebuconazole in soil,which showed good separating result,high sensitivity,good reproducibility, pretreatment with simple operation.%建立快速溶剂萃取–气相色谱质谱法测定土壤中戊唑醇残留量的分析方法.土壤样品经ASE–350快速溶剂萃取仪萃取,萃取液用硅酸镁(弗罗里硅土)柱净化浓缩,然后用选择离子监测/全扫描(SIM/SCAN)模式,气相色谱–质谱法测定土壤中的戊唑醇含量.该方法检出限为0.008 mg/kg,加标回收率为84.0%~97.5%,测定结果的相对标准偏差为2.2%~11.6%(n=6).该方法具有分离效果好,灵敏度高,重现性好,前处理操作简便等优点,可用于测定土壤中戊唑醇的残留量.

  1. Effect of solvent extraction on Tunisian esparto wax composition

    Directory of Open Access Journals (Sweden)

    Saâd Inès

    2016-08-01

    Full Text Available The increase of needs for renewable and vegetable based materials will help to drive the market growth of vegetable waxes. Because of their highly variable composition and physicochemical properties, plant waxes have found numerous applications in the: food, cosmetic, candle, coating, polish etc... The aim of this project is to determine the effect of solvent extraction (petroleum ether and ethanol on Tunisian esparto wax composition. The GC-MS was applied in order to determine the waxes compositions. Then, physicochemical parameters of these two samples of waxes: acid value, saponification value, iodine value and melting point were measured in order to deduct their properties and possible fields of uses. Results showed that esparto wax composition depended on the solvent extraction and that major components of the two samples of waxes were: alkanes, esters of fatty acids and phenols. Furthermore, esparto waxes were characterized by an antioxidant and antibacterial activities but the potential of these activities depended on the solvent of wax extraction.

  2. Supercritical water oxidation of spent extraction solvent simulants

    Institute of Scientific and Technical Information of China (English)

    王帅; 秦强; 陈土方方; 夏晓彬; 马洪军; 乔延波; 何柳斌

    2015-01-01

    The rapid development of nuclear technology has led to more liquid organic radioactive wastes. Different from the regular aqueous radioactive wastes, these liquids possess a higher hazard potential and cannot be disposed through the conventional methods due to their radioactivity and chemical nature. Spent extraction solvent is a kind of common liquid organic radioactive wastes. In this work, tri-butyl phosphate (TBP), which is more difficult to degrade in the spent extraction solvent, was used as the model compound. Influences of reaction conditions on total organic carbon (TOC) removal and the volume percentage of each gas component under supercritical water oxidation (SCWO) were studied. The SCWO behaviors of spent extraction solvent simulants were studied under the optimal conditions derived from the TBP experiment. The SCWO experiments were studied at 400–550◦C, oxidant stoichiometric ratio of 0–200%, feed concentration of 1.5%–4%and pressure of 25 MPa for 15–75 s. The results show that the TOC removal of the simulants was greater than 99.7%and CH4, H2 and CO were not detected at 550◦C, 25 MPa, oxidant stoichiometric ratio of 150%, feed concentration of 3%, and residence time of 30 s.

  3. Hydrophilic actinide complexation studied by solvent extraction radiotracer technique

    Energy Technology Data Exchange (ETDEWEB)

    Rydberg, J. [Chalmers Univ. of Technology, Goeteborg (Sweden). Dept. of Nuclear Chemistry and Radiochemistry Consultant Group, Vaestra Froelunda (Sweden)

    1996-10-01

    Actinide migration in the ground water is enhanced by the formation of water soluble complexes. It is essential to the risk analysis of a wet repository to know the concentration of central atoms and the ligands in the ground water, and the stability of complexes formed between them. Because the chemical behavior at trace concentrations often differ from that at macro concentrations, it is important to know the chemical behavior of actinides at trace concentrations in ground water. One method used for such investigations is the solvent extraction radiotracer (SXRT) technique. This report describes the SXRT technique in some detail. A particular reason for this analysis is the claim that complex formation constants obtained by SXRT are less reliable than results obtained by other techniques. It is true that several difficulties are encountered in the application of SXRT technique to actinide solution, such as redox instability, hydrophilic complexation by side reactions and sorption, but it is also shown that a careful application of the SXRT technique yields results as reliable as by any other technique. The report contains a literature survey on solvent extraction studies of actinide complexes formed in aqueous solutions, particularly by using the organic reagent thenoyltrifluoroacetone (TTA) dissolved in benzene or chloroform. Hydrolysis constants obtained by solvent extraction are listed as well as all actinide complexes studied by SX with inorganic and organic ligands. 116 refs, 11 tabs.

  4. Ultrasound induced green solvent extraction of oil from oleaginous seeds.

    Science.gov (United States)

    Sicaire, Anne-Gaëlle; Vian, Maryline Abert; Fine, Frédéric; Carré, Patrick; Tostain, Sylvain; Chemat, Farid

    2016-07-01

    Ultrasound-assisted extraction of rapeseed oil was investigated and compared with conventional extraction for energy efficiency, throughput time, extraction yield, cleanness, processing cost and product quality. A multivariate study enabled us to define optimal parameters (7.7 W/cm(2) for ultrasonic power intensity, 40 °C for processing temperature, and a solid/liquid ratio of 1/15) for ultrasound-assisted extraction of oil from oilseeds to maximize lipid yield while reducing solvent consumption and extraction time using response surface methodology (RSM) with a three-variable central composite design (CCD). A significant difference in oil quality was noted under the conditions of the initial ultrasound extraction, which was later avoided using ultrasound in the absence of oxygen. Three concepts of multistage cross-current extraction were investigated and compared: conventional multistage maceration, ultrasound-assisted maceration and a combination, to assess the positive impact of using ultrasound on the seed oil extraction process. The study concludes that ultrasound-assisted extraction of oil is likely to reduce both economic and ecological impacts of the process in the fat and oil industry.

  5. Microwave accelerated solvent-free synthesis of flavanones

    Energy Technology Data Exchange (ETDEWEB)

    Sagrera, Gabriel J. [Universidad de la Republica, Montevideo (Uruguay). Facultad de Ciencias. Dept. de Quimica Organica]. E-mail: gseoane@fq.edu.uy; Seoane, Gustavo A. [Universidad de la Republica, Montevideo (Uruguay). Facultad de Quimica

    2005-07-15

    Microwave irradiation of chalcones under solvent-free conditions resulted in a 'green-chemistry' procedure for the preparation of flavanones in very good yields. Using an unmodified household microwave oven, different mineral supports and catalysts were tested. By irradiation of chalcones with 30% TFA over silica gel, eleven known flavanones and five new compounds were prepared in high yields. (author)

  6. 加速溶剂萃取/气相色谱-负化学电离质谱法对土壤中毒杀芬的测定研究%Detection of Toxaphene in Soil by Accelerated Solvent Extraction/GC-NCI MS

    Institute of Scientific and Technical Information of China (English)

    谢原利; 饶竹; 王晓华; 王沫

    2009-01-01

    A method has been developed for the determination of toxaphene in soil by gas chromatography-negative chemical ionization mass spectrometry(GC-NCI MS) with accelerated solvent extraction(ASE).The experimental conditions were investigated on the basis of the optimization of ASE conditions,and the optimal conditions were obtained as follows: extraction solvent: hexane-actone(1 : 1,by volume),system pressure:12.4 MPa,extraction temperature:100 ℃,extraction time :10 min,cycling twice.The extract was cleaned up by passing through Cleanert PestiCarb and florisil solid phase extraction cartridge.The elute was evaporated to dryness under nitrogen to 1.0 mL and the quantitative analysis of toxaphene was performed by GC-MS.The linear range was 0.3-3 000 ng/g for the total toxaphene),the detection limits of toxaphene ranged from 0.10 to 1.00 ng/g,and the spiked standard recoveries were between 86% and 104% with the relative standard deviations ranging from 6.8% to 13.5%(n=7).The method is accurate,simple,and rapid,and adapts for inspection of toxaphene in soil.%建立了加速溶剂萃取/气相色谱-负化学电离质谱法测定土壤中毒杀芬的方法.在加速溶剂萃取实验条件优化的基础上,确定了最佳实验条件:系统压力12.4 MPa,萃取溶剂为正己烷-丙酮(体积比1 : 1),萃取温度100 ℃,静态萃取时间10 min,循环2次.萃取液经活性炭与弗罗里硅土复合小柱净化后,氮吹至1.0 mL,于GC-MS仪上测定.结果表明,毒杀芬的线性范围为0.3 ~3 000 ng/g(毒杀芬总量),相关系数均不小于0.999 0,方法检出限为0.10 ~1.00 ng/g,平均回收率为86% ~104%,相对标准偏差(n=7)为6.8% ~13.5%.

  7. An appropriate solvent for the preparation of Prasaplai extract

    Directory of Open Access Journals (Sweden)

    Prasan Tangyuenyongwatana

    2009-11-01

    Full Text Available Prasaplai is a Thai traditional formulation for relieving dysmenorrhea and adjusting the cycle of menstruation. Threefatty acid esters, (E-4-(3,4-dimethoxyphenylbut-3-en-1-yl linoleate (1, (E-4-(3,4-dimethoxyphenylbut-3-en-1-yl oleate(2 and (E-4-(3,4-dimethoxyphenylbut-3-en-1-yl palmitate (3, were formed during storage by the interaction of componentsin the preparation. The recommended dose (1.0 g of Prasaplai was separately extracted by exhaustive sonication with three different solvents; which are hexane, 40% ethanol and distilled water, and yielded 26.70±0.11 mg (2.7% w/w, 33.96± 0.05 mg (3.40% w/w, and 49.83±0.30 mg (4.98% w/w, respectively. The crude extracts were analyzed by HPLC for contents of the four major compounds i.e (E-1-(3,4-dimethoxyphenylbut-3-en-1-ol (compound D, (E-1-(3,4-dimethoxyphenylbutadiene (DMPBD, piperine, -asarone, and three artifacts. The results showed that only the hexane extractcontained the artifacts while the 40% ethanol extract contained the maximum amounts of the major active anti-inflammatorycomponents, and water extract contained only compound D. These results suggest that the 40% ethanol extract should be theappropriate extract for the preparation of Prasaplai in modern dosage forms due to the high content of active anti-inflammatory agents in the extract.

  8. Phenolic Content and Antioxidant Activity of Hibiscus cannabinus L. Seed Extracts after Sequential Solvent Extraction

    Directory of Open Access Journals (Sweden)

    Shahid Iqbal

    2012-10-01

    Full Text Available A sequential solvent extraction scheme was employed for the extraction of antioxidant compounds from kenaf (Hibiscus cannabinus L. seeds. Yield of extracts varied widely among the solvents and was the highest for hexane extract (16.6% based on dry weight basis, while water extract exhibited the highest total phenolic content (18.78 mg GAE/g extract, total flavonoid content (2.49 mg RE/g extract, and antioxidant activities (p < 0.05. DPPH and hydroxyl radical scavenging, β-carotene bleaching, metal chelating activity, ferric thiocyanate and thiobarbituric acid reactive substances assays were employed to comprehensively assess the antioxidant potential of different solvent extracts prepared sequentially. Besides water, methanolic extract also exhibited high retardation towards the formation of hydroperoxides and thiobarbituric acid reactive substances in the total antioxidant activity tests (p < 0.05. As conclusion, water and methanol extracts of kenaf seed may potentially serve as new sources of antioxidants for food and nutraceutical applications.

  9. Final Report - Energy Reduction and Advanced Water Removal via Membrane Solvent Extraction Technology

    Energy Technology Data Exchange (ETDEWEB)

    Reed, John; Fanselow, Dan; Abbas, Charles; Sammons, Rhea; Kinchin, Christopher

    2014-08-06

    3M and Archer Daniels Midland (ADM) collaborated with the U.S. Department of Energy (DOE) to develop and demonstrate a novel membrane solvent extraction (MSE) process that can substantially reduce energy and water consumption in ethanol production, and accelerate the fermentation process. A cross-flow membrane module was developed, using porous membrane manufactured by 3M. A pilot process was developed that integrates fermentation, MSE and vacuum distillation. Extended experiments of 48-72 hours each were conducted to develop the process, verify its performance and begin establishing commercial viability.

  10. Advanced integrated solvent extraction and ion exchange systems

    Energy Technology Data Exchange (ETDEWEB)

    Horwitz, P. [Argonne National Lab., IL (United States)

    1996-10-01

    Advanced integrated solvent extraction (SX) and ion exchange (IX) systems are a series of novel SX and IX processes that extract and recover uranium and transuranics (TRUs) (neptunium, plutonium, americium) and fission products {sup 90}Sr, {sup 99}Tc, and {sup 137}Cs from acidic high-level liquid waste and that sorb and recover {sup 90}Sr, {sup 99}Tc, and {sup 137}Cs from alkaline supernatant high-level waste. Each system is based on the use of new selective liquid extractants or chromatographic materials. The purpose of the integrated SX and IX processes is to minimize the quantity of waste that must be vitrified and buried in a deep geologic repository by producing raffinates (from SX) and effluent streams (from IX) that will meet the specifications of Class A low-level waste.

  11. A short review of headspace extraction and ultrasonic solvent extraction for honey volatiles fingerprinting

    OpenAIRE

    Jerković, I.; Marijanović, Z.

    2009-01-01

    Honey volatiles exhibit a potential role in distinguishing honeys as a function of botanical origin, but heating of honey generates artefacts such as compounds of Strecker degradation and Maillard reaction products. This short review is focused on the most recently applied methods for honey volatiles fingerprinting (without generation of thermal artefacts): headspace extraction (dynamic headspace extraction (DHE), headspace solid-phase microextraction (HS-SPME)) and ultrasonic solvent extract...

  12. Extraction of hydrocarbons from microalga Botryococcus braunii with switchable solvents.

    Science.gov (United States)

    Samorì, Chiara; Torri, Cristian; Samorì, Giulia; Fabbri, Daniele; Galletti, Paola; Guerrini, Franca; Pistocchi, Rossella; Tagliavini, Emilio

    2010-05-01

    Lipid extraction is a critical step in the development of biofuels from microalgae. Here a new procedure was proposed to extract hydrocarbons from dried and water-suspended samples of the microalga Botryococcus braunii by using switchable-polarity solvents (SPS) based on 1,8-diazabicyclo-[5.4.0]-undec-7-ene (DBU) and an alcohol. The high affinity of the non-ionic form of DBU/alcohol SPS towards non-polar compounds was exploited to extract hydrocarbons from algae, while the ionic character of the DBU-alkyl carbonate form, obtained by the addition of CO(2), was used to recover hydrocarbons from the SPS. DBU/octanol and DBU/ethanol SPS were tested for the extraction efficiency of lipids from freeze-dried B. braunii samples and compared with n-hexane and chloroform/methanol. The DBU/octanol system was further evaluated for the extraction of hydrocarbons directly from algal culture samples. DBU/octanol exhibited the highest yields of extracted hydrocarbons from both freeze-dried and liquid algal samples (16% and 8.2% respectively against 7.8% and 5.6% with n-hexane).

  13. Deep eutectic solvents as novel extraction media for protein partitioning.

    Science.gov (United States)

    Zeng, Qun; Wang, Yuzhi; Huang, Yanhua; Ding, Xueqin; Chen, Jing; Xu, Kaijia

    2014-05-21

    Four kinds of green deep eutectic solvent (DES) were synthesized, including choline chloride (ChCl)-urea, tetramethylammonium chloride (TMACl)-urea, tetrapropylammonium bromide (TPMBr)-urea and ChCl-methylurea. An aqueous two-phase system (ATPS) based ChCl-urea DES was studied for the first time for the extraction of bovine serum albumin (BSA). Single factor experiments proved that the extraction efficiency of BSA was influenced by the mass of the DES, concentration of K2HPO4 solution, separation time and extraction temperature. The optimum conditions were determined through an orthogonal experiment with the four factors described above. The results showed that under the optimum conditions, the average extraction efficiency could reach up to 99.94%, 99.72%, 100.05% and 100.05% (each measured three times). The relative standard deviations (RSD) of extraction efficiencies in precision, repeatability and stability experiments were 0.5533% (n = 5), 0.8306% (n = 5) and 0.9829% (n = 5), respectively. UV-vis and FT-IR spectra confirmed that there were no chemical interactions between BSA and the DES in the extraction process, and the CD spectra proved that the conformation of BSA did not change after extraction. The conductivity, DLS and TEM were combined to investigate the microstructure of the top phase and the possible mechanism for the extraction. The results showed that hydrophobic interactions, hydrogen bonding interactions and the salting-out effect played important roles in the transfer process, and the aggregation and surrounding phenomenon were the main driving forces for the separation. All of these results proved that ionic liquid (IL)-based ATPSs could potentially be substituted with DES-based ATPSs to offer new possibilities in the extraction of proteins.

  14. Ultrasonic-assisted extraction of essential oil from Botryophora geniculate using different extracting solvents

    Science.gov (United States)

    Habibullah, Wilfred, Cecilia Devi

    2016-11-01

    This study compares the performance of ionic liquids to substitute conventional solvents (hexane, dichloromethane and methanol) to extract essential oil from Botryophora geniculate plant. Two different Ionic liquids ([C3MIM][Ac], [C4MIM][Ac]) with co-solvent diethyl ether were used in the ultrasonic-assisted extraction. The effect of various experimental conditions such as time, temperature and solvent were studied. Gas chromatography-mass spectroscopy (GC-MS) was used to analyze essential oils. The results showed that in ultrasonic-assisted extraction using ionic liquids as a solvent gave highest yield (9.5%) in 30 min at temperature 70°C. When using ultrasonic bath with hexane, dichloromethane and methanol, yields was (3.34%), (3.6%) and (3.81%) at 90 min, respectively were obtained. The ultrasonic-assisted extraction under optimal extraction conditions (time 30 min, temperature of 70°C) gave the best yield for the essential oil extraction.

  15. Effect of Extraction Solvent/Technique on the Antioxidant Activity of Selected Medicinal Plant Extracts

    Directory of Open Access Journals (Sweden)

    Bushra Sultana

    2009-06-01

    Full Text Available Theeffects of four extracting solvents [absolute ethanol, absolute methanol, aqueous ethanol (ethanol: water, 80:20 v/v and aqueous methanol (methanol: water, 80:20 v/v] and two extraction techniques (shaking and reflux on the antioxidant activity of extracts of barks of Azadirachta indica, Acacia nilotica, Eugenia jambolana, Terminalia arjuna, leaves and roots of Moringa oleifera, fruit of Ficus religiosa,and leaves of Aloe barbadensis were investigated. The tested plant materials contained appreciable amounts of total phenolic contents (0.31-16.5 g GAE /100g DW, total flavonoid (2.63-8.66 g CE/100g DW; reducing power at 10 mg/mL extract concentration (1.36-2.91, DPPH. scavenging capacity (37.2-86.6%, and percent inhibition of linoleic acid (66.0-90.6%. Generally higher extract yields, phenolic contents and plant material antioxidant activity were obtained using aqueous organic solvents, as compared to the respective absolute organic solvents. Although higher extract yields were obtained by the refluxing extraction technique, in general higher amounts of total phenolic contents and better antioxidant activity were found in the extracts prepared using a shaker.

  16. Terra-Kleen Response Group, Inc. Solvent Extraction Technology Rapid Commercialization Initiative Report

    Science.gov (United States)

    Terra-Kleen Response Group Inc. (Terra-Kleen), has commercialized a solvent extraction technology that uses a proprietary extraction solvent to transfer organic constituents from soil to a liquid phase in a batch process at ambient temperatures. The proprietary solvent has a rel...

  17. Terra-Kleen Response Group, Inc. Solvent Extraction Technology Rapid Commercialization Initiative Report

    Science.gov (United States)

    Terra-Kleen Response Group Inc. (Terra-Kleen), has commercialized a solvent extraction technology that uses a proprietary extraction solvent to transfer organic constituents from soil to a liquid phase in a batch process at ambient temperatures. The proprietary solvent has a rel...

  18. The role of aggregate formation in solvent extraction of calcium

    Energy Technology Data Exchange (ETDEWEB)

    Gaonkar, A.G.; Neuman, R.D.

    1986-09-01

    In solvent extraction processes involving hydrometallurgical separations, spent nuclear fuel reprocessing, and nuclear waste processing operations, metal ions transfer across the boundary between two immiscible liquids. Hence, the properties of the liquid/liquid interface can often influence the extraction process. This suggests that one, therefore, should be able to control the extraction rate by proper manipulation of the nature of the liquid/liquid interface. In an earlier communication (1) from this laboratory, aggregates, possibly reversed micelles, were proposed to form in the system di(2-ethylhexyl)phosphoric acid (HDEHP)/n-hexane/CaCl/sub 2/ solution under certain conditions. The objective of the present study was to determine whether the amount of calcium extracted and the rate of extraction become significant when reversed micelles form. The interfacial tension (..gamma..), equilibrium distribution coefficient (K/sub d/), and mass transfer coefficient (k/sub ao/) were obtained for the system HDEHP/n-hexane/0.01 mol dm/sup -3/ CaCl/sub 2/ solution. 11 refs., 4 figs.

  19. Investigation of aggregation in solvent extraction of lanthanides by acidic extractants (organophosphorus and naphthenic acid)

    Science.gov (United States)

    Zhou, N.; Wu, J.; Yu, Z.; Neuman, R.D.; Wang, D.; Xu, G.

    1997-01-01

    Three acidic extractants (I) di(2-ethylhexyl) phosphoric acid (HDEHP), (II) 2-ethylhexyl phosphonic acid mono-2-ethylhexyl ester (HEHPEHE) and (III) naphthenic acid were employed in preparing the samples for the characterization of the coordination structure of lanthanide-extractant complexes and the physicochemical nature of aggregates formed in the organic diluent of the solvent extraction systems. Photo correlation spectroscopy (PCS) results on the aggregates formed by the partially saponified HDEHP in n-heptane showed that the hydrodynamic radius of the aggregates was comparable to the molecular dimensions of HDEHP. The addition of 2-octanol into the diluent, by which the mixed solvent was formed, increased the dimensions of the corresponding aggregates. Aggregates formed from the lanthanide ions and HDEHP in the organic phase of the extraction systems were found very unstable. In the case of naphthenic acid, PCS data showed the formation of w/o microemulsion from the saponified naphthenic acid in the mixed solvent. The extraction of lanthanides by the saponified naphthenic acid in the mixed solvent under the given experimental conditions was a process of destruction of the w/o microemulsion. A possible mechanism of the breakdown of the w/o microemulsion droplets is discussed.

  20. 加速溶剂萃取-气相色谱质谱法测定海洋沉积物中多氯联苯残留%Determination of polychlorinated biphenyls residues in marine sediments using accelerated solvent extraction with gas chromatog raphy-mass spectrometry

    Institute of Scientific and Technical Information of China (English)

    贺玉林; 刘泽伟; 邹潍力; 卢伟华; 胡浩光

    2012-01-01

    A rapid and accurate method was developed for the determination of polychlorinated biphenyls ( PCBs) residues in marine sediments by accelerated solvent extraction( ASE) and gas chromatography-mass spectrometry( GC-MS) . The target analytes were extracted with hexane/acetone(1: 1 ,v/v) by ASE and cleaned up by composite silica gel column and graphitization carbon column. The results demonstrated that the method detection limits was (0. 005 -0. 038) × 10-9 for PCBs( wet weight). The recovery percentages and RSD of two-level spiked samples were 68. 5% - 108. 4% and 2.1% -11.8% for PCBs, respectively. The method was precise, sensitive, and highly efficient in extraction, and has been applied in the actual POPs monitoring in sediments of marine environment.%样品采用加速溶剂萃取,萃取液依次经复合硅胶和石墨化炭黑柱净化后,采用GC-MS法测定样品中的多氯联苯残留.结果表明,方法检出限为(0.005 ~0.038)×10-9(湿重),样品加标回收率为68.5%~ 108.4%,RSD为2.1%~11.8%.本方法具有提取效率高,净化效果好,回收率高,准确灵敏等优点,可应用于海洋沉积物中多氯联苯等持久性有机污染物残留的监测.

  1. Application of deep eutectic solvents in the extraction and separation of target compounds from various samples.

    Science.gov (United States)

    Tang, Baokun; Zhang, Heng; Row, Kyung Ho

    2015-03-01

    Deep eutectic solvents, as a new type of eco-friendly solvent, have attracted increasing attention in chemistry for the extraction and separation of target compounds from various samples. To summarize the application of deep eutectic solvents, this review highlights some of the unique properties of deep eutectic solvents and deep-eutectic-solvent-based materials, as well as their applications in extraction and separation. In this paper, the available data and references in this field are reviewed to summarize the application developments of deep eutectic solvents. Based on the development of deep eutectic solvents, the exploitation of new deep eutectic solvents and deep-eutectic-solvent-based materials are expected to diversify into extraction and separation. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  2. A Study for Extraction Kinetics of Β-Carotene from Oven Dried Carrot by Solvent Extraction

    Directory of Open Access Journals (Sweden)

    Sudipta Das

    2014-06-01

    Full Text Available The main aim of this work was to study the kinetics of the extraction of β-carotene by solvent (ethanol extraction from carrots dried at 50ºC in an oven. The moisture content after drying was 11±1.5% (dry weight basis. Extraction time was 5 hours and extraction process was carried out at 30ºC. The ratio of Carrot (gm: ethanol (ml of 1:60 was maintained throughout the extraction process. The experimental data of extracted β- Carotene yield during solvent extraction were modeled with seven different mathematical models, including Power law, Peleg, Weinbull’s equation, Pseudo 2nd order, Intraparticle diffusion, Logarithmic, Weinbull’s distribution and one RSM model developed in this study. Pseudo 2nd order model was best fitted model (R2 - 0.99, χ 2 - 0.0091, RMSE- 0.1566, MAE- 0.0115 to describe extraction kinetics of β-carotene from carrot. The extraction time has significant effect on extraction process at p<0.05 level.

  3. Studies of extraction solvent technique. Application in a practice case; Estudios de tratabilidad de la tecnologia de extraccion por solvente. Aplicacion a un caso practico

    Energy Technology Data Exchange (ETDEWEB)

    Susaeta, I.; Salas, O.; Gorostiza, I.; Bargos, Tx.

    1999-11-01

    The extraction for solvent is a technique that consists in an use a solvent in order to separate organic dangerous pollutants of floors, silts and residuals. The extraction for solvent dons`t destroy the pollutants but rather concentrates them so that it is easier and economically more attractive their hind destruction. A process of extraction for solvent would undertake the following steps: Preparation of the material to extract. Extraction properly happiness. Separation of the concentrated pollutants of the solvent. Recovery of the residual solvent. Treatment of the separate pollutants. (Author) 12 refs.

  4. Solvent extraction of chlorinated compounds from soils and hydrodechlorination of the extract phase.

    Science.gov (United States)

    Murena, Fabio; Gioia, Francesco

    2009-03-15

    The remediation of soils contaminated with chlorinated compounds was investigated. The process consists of solvent extraction followed by catalytic hydroprocessing (hydrodechlorination) of the extract phase. A mixture of ethylacetate-acetone-water (E-A-W) was adopted as solvent in the extraction process. Tests of extraction of chlorobenzene from a model contaminated soil were carried out and the Langmuir adsorption equation was characterized. The solvent, contaminated with different chlorinated compounds was then hydrotreated with a Pd/C catalyst. The chlorinated compounds tested are: chlorobenzene, hexachlorobenzene and hexachloroethane at various initial concentrations. The reaction runs were carried out at room temperature and at a hydrogen pressure of 1bar. Hydrotreating of these compounds takes place according to a Langmuir-Hinshelwood mechanism whose kinetic parameters were determined. The experiments show that high destruction efficiencies may be reached in reasonably short times, particularly for hexachloroethane. Longer times are necessary for the aromatic compounds (chlorobenzene and hexachlorobenzene) for which the CCl bond is much stronger than that in the aliphatic compound. Time for a 95% destruction efficiency for all experimental runs was determined. A noteworthy finding is that ethylacetate and acetone do not undergo any reaction during hydrotreating. Thus the treated extract solution may be recycled inasmuch as it conserves its full extracting capacity towards chlorinated compounds. A limitation in recycling is the inhibiting effect of benzene on the HDCl rate: benzene produced by HDCl of chlorinated compounds, accumulates in the solvent mixture in the event of recycling. Simulation of the process with the recycling of the solvent was carried out, accounting for the inhibiting effect of benzene.

  5. Ion Exchange and Solvent Extraction: Supramolecular Aspects of Solvent Exchange Volume 21

    Energy Technology Data Exchange (ETDEWEB)

    Gloe, Karsten [Technischen Universität Dresden; Tasker, Peter A [ORNL; Oshima, Tatsuya [University of Miyazaki; Watarai, Hitoshi [Institute for NanoScience Design at Osaka University; Nilsson, Mikael [University of California, Irvine

    2013-01-01

    Preface The theme of supramolecular chemistry (SC), entailing the organization of multiple species through noncovalent interactions, has permeated virtually all aspects of chemical endeavor over the past several decades. Given that the observed behavior of discrete molecular species depends upon their weak interactions with one another and with matrix components, one would have to conclude that SC must indeed form part of the fabric of chemistry itself. A vast literature now serves to categorize SC phenomena within a body of consistent terminology. The word supramolecular itself appears in the titles of dozens of books, several journals, and a dedicated encyclopedia. Not surprisingly, the theme of SC also permeates the field of solvent extraction (SX), inspiring the framework for this volume of Ion Exchange and Solvent Extraction. It is attempted in the six chapters of this volume to identify both how supramolecular behavior occurs and is studied in the context of SX and how SC is influencing the current direction of SX. Researchers and practitioners have long dealt with supramolecular interactions in SX. Indeed, the use of polar extractant molecules in nonpolar media virtually assures that aggregative interactions will dominate the solution behavior of SX. Analytical chemists working in the 1930s to the 1950s with simple mono- and bidentate chelating ligands as extractants noted that extraction of metal ions obeyed complicated mass-action equilibria involving complex stoichiometries. As chemists and engineers developed processes for nuclear and hydrometallurgical applications in the 1950s and 1960s, the preference for aliphatic diluents only enhanced the complexity and supramolecular nature of extraction chemistry. Use of physical techniques such as light scattering and vapor-pressure measurements together with various spectroscopic methods revealed organic-phase aggregates from well-defined dimers to small aggregates containing a few extractant molecules to large

  6. Determination of Organophosphorus Pesticides in Soil Using Accelerated Solvent Extraction and Gas Chromatography and Negative Chemical Ionization Mass Spectrometry%加速溶剂萃取-气相色谱-负化学离子化质谱法测定土壤中有机磷农药

    Institute of Scientific and Technical Information of China (English)

    林长青; 张纯淳; 李钟瑜; 高鹏

    2014-01-01

    An effective method for trace analysis of organophosphorus pesticides in soil was developed using accelerated solvent extraction ( ASE) followed by gas chromatography-electron ionization-mass spectrometry ( GC-EI-MS) and gas chromatography-negative chemical ionization- mass spectrometry ( GC-NCI-MS ) . The results show that both GC-EI-MS and GC-NCI-MS are sufficient for the daily analysis. GC-EI-MS method has an extensive application scope and is easy to operate. Also the GC-NCI-MS method has advantages in selectivity and sensitivity.%用加速溶剂萃取法( ASE)萃取土壤中的有机磷农药,用气相色谱-负化学离子化质谱法( GC-NCI-MS)进行测定,并与气相色谱-电子轰击电离质谱法( GC-EI-MS)进行了对比。结果表明,EI法和NCI法均能满足目前的有机磷农药的分析需要。 GC-EI-MS的适用范围比较广,操作比较简单;GC-NCI-MS在选择性和灵敏度等方面均具有较强优势。

  7. 21 CFR 173.280 - Solvent extraction process for citric acid.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Solvent extraction process for citric acid. 173.280... extraction process for citric acid. A solvent extraction process for recovery of citric acid from conventional Aspergillus niger fermentation liquor may be safely used to produce food-grade citric acid...

  8. Rapid determination of pesticide multiresidues in vegetables and fruits by accelerated solvent extraction coupled with online gel permeation chromatography-gas chromatography-mass spectrometry%加速溶剂萃取-在线凝胶渗透色谱-气相色谱-质谱联用法快速测定蔬菜和水果中多农药残留

    Institute of Scientific and Technical Information of China (English)

    欧阳运富; 唐宏兵; 吴英; 李贵英

    2012-01-01

    A novel method was developed for the rapid determination of 22 representative pesticide residues in vegetables and fruits based on accelerated solvent extraction (ASE) coupled with online gel permeation chromatography-gas chromatography-mass spectrometry ( GPC-GC-MS). The sample was extracted by accelerated solvent extraction with dichloromethane-ace-tone (1:1 , v/v) and purified with a carbon/NH;column, evaporated to dryness by nitrogen, then dissolved in cyclohexane-acetone (7:3, v/v), and finally identified and quantified by GPC-GC-MS system in selected ion monitoring (SIM) mode. The results showed that the linearities of the 22 pesticides were good in their linear ranges. The limits of detection (S/N = 3 ) were 0. 3 - 1. 8μg/kg. The limits of quantification (S/N =10) ranged from 1 -6 jig/kg. The recoveries for all at three spiked levels in Chinese cabbages and apples ranged from 70. 5% to 107. 5% with the relative standard deviations (RSDs) of 2.1% - 8.7%. The proposed method is accurate, sensitive and highly efficient in the extraction, and can be used for the quick determination of the pesticide multiresidues in vegetables and fruits.%建立了加速溶剂萃取-在线凝胶渗透色谱-气相色谱-质谱联用(GPC-GC-MS)快速测定蔬菜、水果中代表性农药残留的检测方法.样品经二氯甲烷-丙酮(1∶1,v/v)加速溶剂提取,活性炭柱-氨基柱串联净化,氮吹至干,残留物用环己烷-丙酮(7∶3,v/v)溶解后经GPC-GC-MS系统以选择离子监测(SIM)模式测定.结果表明,22种农药在各自的线性范围内线性关系良好(相关系数不低于0.998 1),检出限(以信噪比(S/N)为3计算)为0.3~1.8μg/kg,定量限(S/N=10)为1~6μg/kg.在2种基质(大白菜、苹果)中3个添加水平下的回收率为70.5% ~107.5%,相对标准偏差为2.1% ~8.7%.该方法提取效率高,定性定量准确、灵敏,可实现对蔬菜、水果中多农药残留的快速检测.

  9. Coal extraction by aprotic dipolar solvents. Final report. [Tetramethylurea, hexa-methylphosphoramide

    Energy Technology Data Exchange (ETDEWEB)

    Sears, J T

    1985-12-01

    The overall goals of this project were to examine the rate and amount of extraction of coals at low temperature by a class of solvents with a generic structure to include tetramethylurea (TMU) and hexa-methylphosphoramide (HMPA) and to examine the nature of the extracted coal chemicals. The class of solvents with similar action, however, can be classified as aprotic, base solvents or, somewhat more broadly, specific solvents. The action of solvents by this last classification was then examined to postulate a mechanism of attack. Experimental work was conducted to explain the specific solvent attack including (1) pure solvent extraction, (2) extraction in mixtures with otherwise inert solvents and inhibitors, and (3) extraction with simultaneous catalytic enhancement attempts including water-gas shift conversion. Thus nuclear magnetic resonance (NMR) and gas-chromatograph mass spectrometer (GC-MS) analysis of extract molecules and extraction with high-pressure CO in TMU (plus 2% H2O) was performed. Effects of solvent additives such as cumene and quinone of large amounts of inert solvents such as tetralin, liminone, or carbon disulfide on extraction were also determined. Results are discussed. 82 refs., 36 figs., 37 tabs.

  10. Effect of Organic Solvents on Microalgae Growth, Metabolism and Industrial Bioproduct Extraction: A Review

    Science.gov (United States)

    Miazek, Krystian; Sulc, Radek; Jirout, Tomas; Aguedo, Mario; Goffin, Dorothee

    2017-01-01

    In this review, the effect of organic solvents on microalgae cultures from molecular to industrial scale is presented. Traditional organic solvents and solvents of new generation-ionic liquids (ILs), are considered. Alterations in microalgal cell metabolism and synthesis of target products (pigments, proteins, lipids), as a result of exposure to organic solvents, are summarized. Applications of organic solvents as a carbon source for microalgal growth and production of target molecules are discussed. Possible implementation of various industrial effluents containing organic solvents into microalgal cultivation media, is evaluated. The effect of organic solvents on extraction of target compounds from microalgae is also considered. Techniques for lipid and carotenoid extraction from viable microalgal biomass (milking methods) and dead microalgal biomass (classical methods) are depicted. Moreover, the economic survey of lipid and carotenoid extraction from microalgae biomass, by means of different techniques and solvents, is conducted. PMID:28677659

  11. Solvent Extraction of Alkaline Earth Metals with Alkylphosphorus Acids

    Institute of Scientific and Technical Information of China (English)

    XUXin; ZHUTun

    2002-01-01

    Solvent extraction equiliria of four main alkaline earth metals (magnesium, calcium, strontium and barium) with di(2-ethylhexyl) phosphoric acid (DEHPA), 2-ethylhexyl phosphonic acid mono-(2-ethylhexyl) ester, di(2,4,4-tri-methylpentyl) phosphinic acid and IR spectra of the extracts have been studied. The selectivity order is dependent of the e/r value and hydration energy of the metal ions. The minor shift of the P→O in IR absorption of the alkaline earth metal extracts indicates that the interaction between the metal ions and P→O is much weaker for alkaline earth metals than for transitional metals. The distribution of the four alkaline earth elements between aqueous solutions and solutions of DEHPA and neutral organophosphorus compunds, tri-n-butyl phosphate (TBP) or tri-octyl phosphine oxide (TOPO) in kerosene have been determined at varying ratio of TBP or TOPO to DEHPA and the positive synergism is observed. The synergic effects is explained by using IR spectra of the loaded organic phase.

  12. Non-polar Solvent Microwave-Assisted Extraction of Volatile Constituents from Dried Zingiber Officinale Rosc.

    Institute of Scientific and Technical Information of China (English)

    YU Yong; WANG Zi-Ming; WANG Yu-Tang; LI Tie-Chun; CHENG Jian-Hua; LIU Zhong-Ying; ZHANG Han-Qi

    2007-01-01

    A new method, non-polar solvent microwave-assisted extraction (NPSMAE), was applied to the extraction of essential oil from Zingiber officinale Rosc. in closed-vessel system. By adding microwave absorption mediumcarbonyl iron powders (CIP) into extraction system, the essential oil was extracted by the non-polar solvent (ether)which can be heated by CIP. The constituents of essential oil obtained by NPSMAE were comparable with those obtained by hydrodistillation (HD) by GC-MS analysis, which indicates that NPSMAE is a feasible way to extract essential oil from dried plant materials. The NPSMAE took much less extraction time (5 min) than HD (180 min),and its extraction efficiency was much higher than that of conventional polar solvent microwave-assisted extraction (PSMAE) and mixed solvent microwave-assisted extraction (MSMAE). It can be a good alternative for the extraction of volatile constituents from dried plant samples.

  13. Sharp Interface Tracking in Rotating Microflows of Solvent Extraction

    Energy Technology Data Exchange (ETDEWEB)

    Glimm, James [Stony Brook Univ., NY (United States); Almeida, Valmor de [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Jiao, Xiangmin [Stony Brook Univ., NY (United States); Sims, Brett [City Univ. (CUNY), NY (United States). Borough of Manhattan Community College; Li, Xaiolin [Stony Brook Univ., NY (United States)

    2013-01-08

    The objective of this project is to develop a specialized sharp interface tracking simulation capability for predicting interaction of micron-sized drops and bubbles in rotating flows relevant to optimized design of contactor devices used in solvent extraction processes of spent nuclear fuel reprocessing. The primary outcomes of this project include the capability to resolve drops and bubbles micro-hydrodynamics in solvent extraction contactors, determining from first principles continuum fluid mechanics how micro-drops and bubbles interact with each other and the surrounding shearing fluid for realistic flows. In the near term, this effort will play a central role in providing parameters and insight into the flow dynamics of models that average over coarser scales, say at the millimeter unit length. In the longer term, it will prove to be the platform to conduct full-device, detailed simulations as parallel computing power reaches the exaflop level. The team will develop an accurate simulation tool for flows containing interacting droplets and bubbles with sharp interfaces under conditions that mimic those found in realistic contactor operations. The main objective is to create an off-line simulation capability to model drop and bubble interactions in a domain representative of the averaged length scale. The technical approach is to combine robust interface tracking software, subgrid modeling, validation quality experiments, powerful computational hardware, and a team with simulation modeling, physical modeling and technology integration experience. Simulations will then fully resolve the microflow of drops and bubbles at the microsecond time scale. This approach is computationally intensive but very accurate in treating important coupled physical phenomena in the vicinity of interfaces. The method makes it possible to resolve spatial scales smaller than the typical distance between bubbles and to model some non-equilibrium thermodynamic features such as finite

  14. Determining an Efficient Solvent Extraction Parameters for Re-Refining of Waste Lubricating Oils

    Directory of Open Access Journals (Sweden)

    Hassan Ali Durrani

    2012-04-01

    Full Text Available Re-refining of vehicle waste lubricating oil by solvent extraction is one of the efficient and cheapest methods. Three extracting solvents MEK (Methyl-Ethyl-Ketone, 1-butanol, 2-propanol were determined experimentally for their performance based on the parameters i.e. solvent type, solvent oil ratio and extraction temperature. From the experimental results it was observed the MEK performance was highest based on the lowest oil percent losses and highest sludge removal. Further, when temperature of extraction increased the oil losses percent also decreased. This is due to the solvent ability that dissolves the base oil in waste lubricating oil and determines the best SOR (Solvent Oil Ratio and extraction temperatures.

  15. 用加速溶剂萃取及制备型高效液相色谱法从烟梗中制取多酚对照品%Preparation of Polyphenol Reference Substance from Peduncle of Tobacco by Accelerated Solvent Extraction and Pre-HPLC

    Institute of Scientific and Technical Information of China (English)

    金诚; 刘汗青; 田孟华; 曹鑫

    2013-01-01

    提出用加速溶剂萃取及制备型高效液相色谱方法从烟梗中提取、制备多酚对照品的方法.样品粉碎后以乙醇(80+-20)溶液为萃取溶剂经加速溶剂萃取仪在110℃静态萃取10 min,提取液氮气吹扫60 s后过MCI树脂和Sephadex LH 20凝胶净化,流出液用丙酮定容后,先通过制备型高效液相色谱初步分离,再通过半制备高效液相色谱进一步分离,得到5个多酚类化合物,经核磁共振波谱法鉴定分别为芸香苷、绿原酸、槲皮素、柚皮素和咖啡酸甲酯.5个多酚类化合物的纯度均大于99%,故可用作多酚对照品.%A method for the extraction and preparation of polyphenol reference substances from peduncle of tobacco by accelerated solvent extraction and pre-HPLC was proposed.The sample was crushed and extracted with ethanol (80+-20) solution under static condition at 110 C for 10 min,and the extract was swept for 60 s by N2-blowing and purified by MCI resin and Sephadex LH 20 gel.The eluate collected was taken up with acetone and used for preliminary separation by pre-HPLC,and for further separation by semi Pre-HPLC,and five polyphenols were obtained,which were identified by NMR to be rutin,chlorogenic acid,quercetin,naringenin and methyl caffeate.The purity of the 5 polyphenols were more than 99%,which could be used as reference materials.

  16. Extraction of polycyclic aromatic hydrocarbons from soot and sediment: solvent evaluation and implications for sorption mechanism.

    Science.gov (United States)

    Jonker, Michiel T O; Koelmans, Albert A

    2002-10-01

    Soot contains high levels of toxic compounds such as polycyclic aromatic hydrocarbons (PAHs). Extraction of PAHs from soot for quantitative analysis is difficult because the compounds are extremely tightly bound to the sorbent matrix. This study was designed to investigate the effect of solvent type on PAH extraction yield, to identify the most optimal solvent for PAH extraction from soot, and to gain insight into the mechanism of PAH sorption to soot in aquatic environments. To that end, different types of soot as well as coal, charcoal, and sediments containing soot-like material were extracted with seven organic solvents. Large differences in extraction recoveries were observed among solvents, with relative values as low as 16% as compared to the best extracting solvent. These differences were much larger for soot than for sediments. Dichloromethane, which to date is the most widely used solvent for soot and sediment extractions, appeared to be the overall worst extractant, whereas toluene/methanol (1:6) gave the best results. Based on extraction yields and solvent properties, extraction of PAHs from soot was explained by a two-step mechanism involving swelling of the sorbent matrix and subsequent displacement of sorbates by solvent molecules. Due to the low displacement capacity of water, desorption of PAHs from soot in the aquatic environment will be strongly limited. Moreover, a certain fraction of the total PAH mass on soot is suggested to be physically entrapped, making it unavailable for partitioning to the aqueous phase.

  17. The solvent absorption-extractive distillation (SAED) process for ethanol recovery from gas/vapor streams

    Energy Technology Data Exchange (ETDEWEB)

    Dale, M.C.

    1993-12-31

    A low energy system for ethanol recovery and dehydration has been developed. This system utilizes a solvent for (1) absorption of ethanol vapors, and then the same solvent for (2) extractive distillation. The ideal solvent for this process would have a high affinity for ethanol, and no affinity for water. Heavy alcohols such as dodecanol, and tridecanol, some phosphorals, and some fatty acids have been determined to meet the desired specifications. These solvents have the effect of making water more volatile than ethanol. Thus, a water stream is taken off initially in the dehydration column, and a near anhydrous ethanol stream is recovered from the ethanol/solvent stripper column. Thus the solvent serves dual uses (1) absorption media, and (2) dehydration media. The SAED process as conceptualized would use a solvent similar to solvents used for direct extractive separation of ethanol from aqueous ethanol solutions.

  18. Secondary amines as switchable solvents for lipid extraction from non-broken microalgae.

    Science.gov (United States)

    Du, Ying; Schuur, Boelo; Samorì, Chiara; Tagliavini, Emilio; Brilman, Derk Willem Frederik

    2013-12-01

    Lipids from algal biomass may provide renewable fuel and chemical feedstock in large quantities. The energy intensity of drying and milling of algae prior to extraction and of solvent recovery afterwards is a major obstacle. The objective is to use switchable solvents to extract oil directly from wet microalgae slurries without the need for drying and milling, and subsequently recover the extracted oil and solvent by simple phase splitting, using CO2 as trigger. In this work secondary amine solvents were investigated for lipids extraction, polarity switching and phase splitting ability upon contacting with CO2. For strain Desmodesmus sp. extraction yields from the wet algal slurries, with and without cell disruption, were comparable with Bligh & Dyer method yields. Oil and solvent recovery via phase separation was realized by CO2 induced phase splitting, making secondary amines a candidate for further development of an energy efficient lipid extraction technology for non-broken microalgae. Copyright © 2013 Elsevier Ltd. All rights reserved.

  19. Deep eutectic solvents as efficient solvent system for the extraction of κ-carrageenan from Kappaphycus alvarezii.

    Science.gov (United States)

    Das, Arun Kumar; Sharma, Mukesh; Mondal, Dibyendu; Prasad, Kamalesh

    2016-01-20

    Three different deep eutectic solvents (DESs) prepared by the complexation of choline chloride with urea, ethylene glycol and glycerol along with their hydrated counterparts were used for the selective extraction of κ-carrageenan from Kappaphycus alvarezii. Upon comparison of the quality of the polysaccharide with the one obtained using water as extraction media as well as the one extracted using widely practiced conventional method, it was found that, the physicochemical as well as rheological properties of κ-carrageenan obtained using DESs as solvents was at par to the one obtained using conventional method and was superior in quality when compared to κ-carrageenan obtained using water as solvent. Considering the tedious nature of the extraction method employed in conventional extraction process, the DESs can be considered as suitable alternative solvents for the facile extraction of the polysaccharide directly from the seaweed. However, among the hydrated and non-hydrated DESs, the hydrated ones were found to be more effective in comparison to their non-hydrated counterparts.

  20. 加速溶剂萃取技术分析谷物中的油脂含量综合研究型实验%A comprehensive experiment of analysing oil content in soy food based on accelerated solvent extraction technique

    Institute of Scientific and Technical Information of China (English)

    陶佳; 杭义萍; 龚华清

    2016-01-01

    从研究型教学的理念出发,开设了“加速溶剂萃取技术分析谷物中的油脂含量”综合研究型实验。阐述了实验选题的目的和意义、实验设计的原理、内容以及实验结果。该实验选题新颖、具有较强的实用性,学生的参与热情较高,能够帮助学生全方位学习实际样品的前处理的原理与分析方法,拓宽学生的视野,培养学生的工程意识。该实验样品成本较低、安全性较高,可作为大学综合化学实验进行推广。%Considering the requirements of high quality food in modern life and the concept of research‐based teaching ,this paper proposes a comprehensive research experiment focused on “The analysis of oil content in soy food based on the accelerated solvent extraction technique ,” the designed mechanism ,content and results are discussed in detail . The teaching practice shows that this novel experiments have not only a strong practicability ,but also a great appeal for students .This lesson could assist the students in studying the pre‐treatment of real samples ,analytical methods and data processing software comprehensively .In addition ,it could broaden students’ horizons and cultivates the students’ engineering consciousness . The sample in experiments is low cost and high safety ,it is suitable to be used as the teaching content of comprehensive analytical chemistry experiment .

  1. Radiation chemistry in solvent extraction: FY2010 Research

    Energy Technology Data Exchange (ETDEWEB)

    Bruce J. Mincher; Leigh R. Martin; Stephen P. Mezyk

    2010-09-01

    This report summarizes work accomplished under the Fuel Cycle Research and Development (FCR&D) program in the area of radiation chemistry during FY 2010. The tasks assigned during FY 2010 included: • Development of techniques to measure free radical reaction kinetics in the organic phase. • Initiation of an alpha-radiolysis program • Initiation of an effort to understand dose rate effects in radiation chemistry • Continued work to characterize TALSPEAK radiation chemistry Progress made on each of these tasks is reported here. Briefly, a method was developed and used to measure the kinetics of the reactions of the •NO3 radical with solvent extraction ligands in organic solution, and the method to measure •OH radical reactions under the same conditions has been designed. Rate constants for the CMPO and DMDOHEMA reaction with •NO3 radical in organic solution are reported. Alpha-radiolysis was initiated on samples of DMDOHEMA in alkane solution using He ion beam irradiation and 211At isotope irradiation. The samples are currently being analyzed for comparison to DMDOHEMA ?-irradiations using a custom-developed mass spectrometric method. Results are also reported for the radiolytic generation of nitrous acid, in ?-irradiated nitric acid. It is shown that the yield of nitrous acid is unaffected by an order-of-magnitude change in dose rate. Finally, recent results for TALSPEAK radiolysis are reported, summarizing the effects on solvent extraction efficiency due to HDEHP irradiation, and the stable products of lactic acid and DTPA irradiation. In addition, results representing increased scope are presented for the radiation chemistry program. These include an investigation of the effect of metal complexation on radical reaction kinetics using DTPA as an example, and the production of a manuscript reporting the mechanism of Cs-7SB radiolysis. The Cs-7SB work takes advantage of recent results from a current LDRD program to understand the fundamental chemistry

  2. Comparison of solvent extraction and solid-phase extraction for the determination of polychlorinated biphenyls in transformer oil.

    Science.gov (United States)

    Mahindrakar, A N; Chandra, S; Shinde, L P

    2014-01-01

    Solid-phase extraction (SPE) of nine polychlorinated biphenyls (PCBs) from transformer oil samples was evaluated using octadecyl (CI8)-bonded porous silica. The efficiency of SPE of these PCBs was compared with those obtained by solvent extraction with DMSO and hexane. Average recoveries exceeding 95% for these PCBs were obtained via the SPE method using small cartridges containing 100mg of 40 pm CI8-bonded porous silica. The average recovery by solvent extraction with DMSO and hexane exceeded 83%. It was concluded that the recoveries and precision for the solvent extraction of PCBs were poorer than those for the SPE.

  3. Kinetics and Thermodynamics of Oil Extraction from Jatropha curcas L. Using Ethanol as a Solvent

    OpenAIRE

    Silmara Bispo dos Santos; Marcio Arêdes Martins; Ana Lívia Caneschi; Paulo Rafael Morette Aguilar; Jane Sélia dos Reis Coimbra

    2015-01-01

    In the study the yield and kinetic and thermodynamic parameters of the oil extraction process from Jatropha curcas L. using ethanol as a solvent were evaluated for different temperatures, moisture contents of the solid phase, and particle sizes. The extraction process yield increased with contact time of solid particles with the solvent until reaching equilibrium (saturation of the solvent), for all the temperatures, moisture contents, and average particle sizes. These parameters significantl...

  4. Secondary amines as switchable solvents for lipid extraction from non-broken microalgae

    NARCIS (Netherlands)

    Du, Y.; Schuur, B.; Samori, C.; Tagliavini, E.; Brilman, D.W.F.

    2013-01-01

    Lipids from algal biomass may provide renewable fuel and chemical feedstock in large quantities. The energy intensity of drying and milling of algae prior to extraction and of solvent recovery afterwards is a major obstacle. The objective is to use switchable solvents to extract oil directly from we

  5. Secondary amines as switchable solvents for lipid extraction from non-broken microalgae

    NARCIS (Netherlands)

    Du, Ying; Schuur, Boelo; Samori, C.; Tagliavini, E.; Brilman, Derk Willem Frederik

    2013-01-01

    Lipids from algal biomass may provide renewable fuel and chemical feedstock in large quantities. The energy intensity of drying and milling of algae prior to extraction and of solvent recovery afterwards is a major obstacle. The objective is to use switchable solvents to extract oil directly from

  6. Secondary amines as switchable solvents for lipid extraction from non-broken microalgae

    NARCIS (Netherlands)

    Du, Ying; Schuur, Boelo; Samori, C.; Tagliavini, E.; Brilman, Derk Willem Frederik

    2013-01-01

    Lipids from algal biomass may provide renewable fuel and chemical feedstock in large quantities. The energy intensity of drying and milling of algae prior to extraction and of solvent recovery afterwards is a major obstacle. The objective is to use switchable solvents to extract oil directly from we

  7. Selective Extraction of Rare Earth Elements from Permanent Magnet Scraps with Membrane Solvent Extraction.

    Science.gov (United States)

    Kim, Daejin; Powell, Lawrence E; Delmau, Lætitia H; Peterson, Eric S; Herchenroeder, Jim; Bhave, Ramesh R

    2015-08-18

    The rare earth elements (REEs) such as neodymium, praseodymium, and dysprosium were successfully recovered from commercial NdFeB magnets and industrial scrap magnets via membrane assisted solvent extraction (MSX). A hollow fiber membrane system was evaluated to extract REEs in a single step with the feed and strip solutions circulating continuously through the MSX system. The effects of several experimental variables on REE extraction such as flow rate, concentration of REEs in the feed solution, membrane configuration, and composition of acids were investigated with the MSX system. A multimembrane module configuration with REEs dissolved in aqueous nitric acid solutions showed high selectivity for REE extraction with no coextraction of non-REEs, whereas the use of aqueous hydrochloric acid solution resulted in coextraction of non-REEs due to the formation of chloroanions of non-REEs. The REE oxides were recovered from the strip solution through precipitation, drying, and annealing steps. The resulting REE oxides were characterized with XRD, SEM-EDX, and ICP-OES, demonstrating that the membrane assisted solvent extraction is capable of selectively recovering pure REEs from the industrial scrap magnets.

  8. Efficient removal of naphthalene-2-ol from aqueous solutions by solvent extraction.

    Science.gov (United States)

    Shao, Jingjing; Cheng, Yan; Yang, Chunping; Zeng, Guangming; Liu, Wencan; Jiao, Panpan; He, Huijun

    2016-09-01

    Naphthalene-2-ol is a typical biologically recalcitrant pollutant in dye wastewater. Solvent extraction of naphthalene-2-ol from aqueous solutions using mixed solvents was investigated. Various extractants and diluents were evaluated, and the effects of volume ratio of extractant to diluent, initial pH, initial concentration of naphthalene-2-ol in aqueous solution, extraction time, temperature, volume ratio of organic phase to aqueous phase (O/A), stirring rate and extraction stages, on extraction efficiency were examined separately. Regeneration and reuse of the spent extractant were also investigated. Results showed that tributyl phosphate (TBP) achieved 98% extraction efficiency for naphthalene-2-ol in a single stage extraction, the highest among the 12 extractants evaluated. Extraction efficiency was optimized when cyclohexane and n-octane were used as diluents. The solvent combination of 20% TBP, 20% n-octanol and 60% cyclohexane (V/V) obtained the maximum extraction efficiency for naphthalene-2-ol, 99.3%, within 20min using three cross-current extraction stages under the following extraction conditions: O/A ratio of 1:1, initial pH of 3, 25°C and stirring rate of 150r/min. Recovery of mixed solvents was achieved by using 15% (W/W) NaOH solution at an O:A ratio of 1:1 and a contact time of 15min. The mixed solvents achieved an extraction capacity for naphthalene-2-ol stably higher than 90% during five cycles after regeneration.

  9. Liquid-liquid equilibrium extraction of ethanol with mixed solvent for bioethanol concentration

    Institute of Scientific and Technical Information of China (English)

    Hiroaki Habaki; Haihao Hu; Ryuichi Egashira

    2016-01-01

    The extraction of ethanol with the solvents of aldehydes mixed with m-xylene was studied for the bioethanol concentration process. Furfural and benzaldehyde were selected as extraction solvents, with which the solubility of water is smal , expecting large distribution coefficient of ethanol. The liquid–liquid two-phase region was the largest with m-xylene solvent, followed by benzaldehyde and furfural. The region of two liquid–liquid phase be-came larger with the mixed solvent of m-xylene and furfural than that with furfural solvent. The NRTL model was applied to the ethanol–water–furfural–m-xylene system, and the model could well express the liquid–liquid equilibrium of the system. For any solvent used in this study, the separation selectivity of ethanol relative to water decreased as the distribution coefficient of ethanol increased. The separation selectivity with m-xylene was the largest among the employed solvents, but the distribution coefficient was the smal est. The solvent mix-ture of furfural and m-xylene showed relatively high distribution coefficient of ethanol and separation selectivity, even in the higher mass fraction of m-xylene in the solvent phase. The ethanol extraction with a countercurrent multistage extractor by a continuous operation was simulated to evaluate the extraction performance. The ethanol content could be concentrated in the extract phase with relatively small number of extraction stages but low yield of ethanol was obtained.

  10. 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.

  11. Solvent extraction, ion chromatography, and mass spectrometry of molybdenum isotopes.

    Science.gov (United States)

    Dauphas, N; Reisberg, L; Marty, B

    2001-06-01

    A procedure was developed that allows precise determination of molybdenum isotope abundances in natural samples. Purification of molybdenum was first achieved by solvent extraction using di(2-ethylhexyl) phosphate. Further separation of molybdenum from isobar nuclides was obtained by ion chromatography using AG1-X8 strongly basic anion exchanger. Finally, molybdenum isotopic composition was measured using a multiple collector inductively coupled plasma hexapole mass spectrometer. The abundances of molybdenum isotopes 92, 94, 95, 96, 97, 98, and 100 are 14.8428(510), 9.2498(157), 15.9303(133), 16.6787(37), 9.5534(83), 24.1346(394), and 9.6104(312) respectively, resulting in an atomic mass of 95.9304(45). After internal normalization for mass fractionation, no variation of the molybdenum isotopic composition is observed among terrestrial samples within a relative precision on the order of 0.00001-0.0001. This demonstrates the reliability of the method, which can be applied to searching for possible isotopic anomalies and mass fractionation.

  12. Comparative study of lipid extraction from microalgae by organic solvent and supercritical CO2.

    Science.gov (United States)

    Cheng, Chen-Hsi; Du, Tz-Bang; Pi, Hsien-Chueh; Jang, Shyue-Ming; Lin, Yun-Huin; Lee, Hom-Ti

    2011-11-01

    Pavlova sp. was employed to evaluate the efficiency of different lipid extraction methods. The microalgal crude lipids content determined using the mixed solvent with ultrasonic method was 44.7 wt.%. The triglyceride content obtained by the mixed solvent method was 15.6 wt.%. The extraction yield was the FAME yield divided by the maximum FAME (15.9 wt.%). The extraction yield was improved by cell disruption prior to extraction, and the highest triglyceride extraction yield of 98.7% was observed using the supercritical fluid extraction (SFE) method with bead-beating. The results indicate that the SFE method is effective and provides higher selectivity for triglyceride extraction though the total lipid extracted was less than that using solvent extraction. Copyright © 2011 Elsevier Ltd. All rights reserved.

  13. Comparison and Combination of Solvent Extraction and Adsorption for Crude Glycerol Enrichment

    OpenAIRE

    Hunsom, Mali; Saila, Payia; Chaiyakam, Penpisuth; Kositnan, Winata

    2016-01-01

    A comparative study of enrichment of crude glycerol via solvent extraction and adsorption was performed at a laboratory scale at ambient temperature (30 oC). Effect of various parameters on the properties of the obtained glycerol including glycerol-, ash- and contaminant contents and color, was explored. The results showed that the enrichment of glycerol by solvent extraction was significantly affected by the solvent type and ratio of solvent to pre-treated crude glycerol. The use of n-C3H7OH...

  14. Studies of solvent extraction properties of s-ethyl-N-(diisopropylthiophosphoryl) dithiocarbamate

    Energy Technology Data Exchange (ETDEWEB)

    Toropova, V.F.; Lazareva, G.A.; Zimin, M.G.; Kamalov, R.M. (Kazanskij Gosudarstvennyj Univ. (USSR))

    1983-09-01

    The results of studying compleXing and solvent extraction properties of thiophosphorylated derivative of dithiocarbamate-S-ethyl-N-(diisopropylthiophosphoryl) dithiocarbomate (TPDTC) and possibilities of its use as analytical reagent are presented. Metal complexes formed by TPDTC are readily extracted by organic solvents. The study of complex extraction by chloroform solution of the reagent versus the medium acidity has shown that the Hg-(2), Ag-, Bi-. Sn-(2), Cu(2) complexes are quantitatively extracted from acid media. Co-(2), Ni-, Cd-, Zn-, Pb(2) complexes are extractable from weakly acid and neutral solutions. Such elements as Fe, Mn, As, Cr, Sb are not extractable from either acid or neutral media.

  15. The extraction of aromatic amino acids with binary and ternary mixtures of hydrophilic solvents

    Science.gov (United States)

    Mokshina, N. Ya.; Pakhomova, O. A.; Niftaliev, S. I.

    2007-11-01

    The extraction of tyrosine and phenylalanine with binary and ternary mixtures of hydrophilic solvents from aqueous salt solutions was studied, and several tendencies were observed. Simplex-lattice planning of experiment was used for the optimization of the composition of solvent mixtures. It was shown that the extraction systems developed could be employed for the almost complete extraction of tyrosine and phenylalanine from aqueous solutions.

  16. Extraction by solvent using microwave and ultrasound-assisted techniques followed by HPLC analysis of Harpagoside from Harpagophytum procumbens and comparison with conventional solvent extraction methods

    OpenAIRE

    Filly, Aurore; Fabiano-Tixier, Anne-Sylvie; Petitcolas, Emmanuel; Mabrouki, Fathi; Chemat, Farid; Ollivier, Évelyne

    2016-01-01

    This research paper presents a quick and ecofriendly technique for the extraction of harpagoside (HS), the active marker of Harpagophytum procumbens (HP), along with a comparison with conventional methods so as to propose an efficient HPLC method. HP is widely used as an anti-inflammatory in phytotherapy. The quality control of the herbal drug and extract calls for a time consuming method of conventional extraction, which involves a high consumption of solvents. In this study, HP has been ...

  17. Ultrasonication-Assisted Solvent Extraction of Quercetin Glycosides from ‘Idared’ Apple Peels

    Directory of Open Access Journals (Sweden)

    Gwendolyn M. Huber

    2011-11-01

    Full Text Available Quercetin and quercetin glycosides are physiologically active flavonol molecules that have been attributed numerous health benefits. Recovery of such molecules from plant matrices depends on a variety of factors including polarity of the extraction solvent. Among the solvents of a wide range of dielectric constants, methanol recovered the most quercetin and its glycosides from dehydrated ‘Idared’ apple peels. When ultra-sonication was employed to facilitate the extraction, exposure of 15 min of ultrasound wavelengths of dehydrated apple peel powder in 80% to 100% (v/v methanol in 1:50 (w:v solid to solvent ratio provided the optimum extraction conditions for quercetin and its glycosides. Acidification of extraction solvent with 0.1% (v/v or higher concentrations of HCl led to hydrolysis of naturally occurring quercetin glycosides into the aglycone as an extraction artifact.

  18. Chemical composition of Artemisia annua L. leaves and antioxidant potential of extracts as a function of extraction solvents.

    Science.gov (United States)

    Iqbal, Shahid; Younas, Umer; Chan, Kim Wei; Zia-Ul-Haq, Muhammad; Ismail, Maznah

    2012-05-21

    This study was conducted to investigate the chemical and nutritional composition of Artemisia annua leaves in addition to determination of antioxidant potential of their extracts prepared in different solvents. Chemical composition was determined by quantifying fat, protein, carbohydrate, fiber, tocopherol, phytate, and tannin contents. Extraction of A. annua leaves, for antioxidant potential evaluation, was carried out using five solvents of different polarities, i.e., hexane, chloroform, ethyl acetate, methanol and water. Antioxidant potential was evaluated by estimating total phenolic (TPC), flavonoid (TFC) contents, ferric reducing antioxidant power (FRAP), Trolox equivalent antioxidant capacity (TEAC), DPPH radical scavenging activity and lipid peroxidation. Efficiency of different solvents was compared for the yield of antioxidant extracts from leaf samples and a clear variation was observed. The highest TPC, TFC, TEAC, DPPH radical scavenging and lowest lipid peroxidation were observed in MeOH extracts, whereas aqueous extract exhibited high ferric reducing antioxidant power; suggesting MeOH to be the most favorable extractant.

  19. Preparation and physicochemical characteristics of polylactide microspheres of emamectin benzoate by modified solvent evaporation/extraction method.

    Science.gov (United States)

    Zhang, Shao Fei; Chen, Peng Hao; Zhang, Fei; Yang, Yan Fang; Liu, De Kun; Wu, Gang

    2013-12-18

    Emamectin benzoate is highly effective against insect pests and widely used in the world. However, its biological activity is limited because of high resistance of target insects and rapid degradation speed in fields. Preparation and physicochemical characterization of degradable microcapsules of emamectin benzoate were studied by modified solvent evaporation/extraction method using polylactide (PLA) as wall material. The influence of different compositions of the solvent in internal organic phase and external aqueous phase on diameter, span, pesticide loading, and entrapment rate of the microspheres was investigated. The results indicated that the process of solvent extraction and the formation of the microcapsules would be accelerated by adding water-miscible organic solvents such as ethyl ether, acetone, ethyl acetate, or n-butanol into internal organic phase and external aqueous phase. Accelerated formation of the microcapsules would result in entrapment rates of emamectin benzoate increased to as high as 97%. In addition, by adding ethanol into the external aqueous phase, diameters would reduce to 6.28 μm, whereas the loading efficiency of emamectin benzoate did not increase. The PLA microspheres prepared under optimum conditions were smoother and more spherical. The degradation rate in PLA microspheres of emamectin benzoate on the 10th day was 4.29 ± 0.74%, whereas the degradation rates of emamectin benzoate in methanol solution and solid technical material were 46.3 ± 2.11 and 22.7 ± 1.51%, respectively. The PLA skeleton had combined with emamectin benzoate in an amorphous or molecular state by using differential scanning calorimetry (DSC) determination. The results indicated that PLA microspheres of emamectin benzoate with high entrapment rate, loading efficiency, and physicochemical characteristics could be obtained by adding water-miscible organic solvents into the internal organic phase and external aqueous phase.

  20. Desulfurization of diesel by oxidation/extraction scheme. Influence of the extraction solvent

    Energy Technology Data Exchange (ETDEWEB)

    Ramirez-Verduzco, L.F.; Torres-Garcia, E.; Gomez-Quintana, R.; Gonzalez-Pena, V.; Murrieta-Guevara, F. [Programa de Tratamiento de Crudo Maya, Instituto Mexicano del Petroleo, Eje Central Lazaro Cardenas 152, CP 07730 Mexico, DF (Mexico)

    2004-11-24

    Due to the future specifications for sulfur content in middle distillate like diesel, a lot of research work has been done to develop alternative methods for desulfurization. This work presents the results for the desulfurization of diesel by an oxidation and extraction (O/E) scheme. This process can be considered like a post-treatment to the traditional hydrodesulfurization. A diesel with 320ppmw of total sulfur was employed to evaluate the elimination of sulfur compounds. The oxidation reaction was carried out with hydrogen peroxide at 30wt.%, in a heterogeneous system with a WO{sub x}/ZrO{sub 2} catalyst at 15wt.% of W; the extraction was performed with four polar solvents. The experiments were done in a batch reactor at 333K and atmospheric pressure. As an average, the sulfur content in the diesel after treatment was 90ppmw. A speciation of the sulfur compounds before and after O/E scheme was also included. Additionally, solubility data of dibenzothiophene sulfone in the polar solvents as a function of temperature were obtained.

  1. Influence of green solvent extraction on carotenoid yield from shrimp (Pandalus borealis) processing waste

    DEFF Research Database (Denmark)

    Razi Parjikolaei, Behnaz; El-Houri, Rime Bahij; Fretté, Xavier

    2015-01-01

    In this work, sunflower oil (SF) and methyl ester of sunflower oil (ME-SF) were introduced as two green solvents for extracting astaxanthin (ASX) from shrimp processing waste. The effects of temperature (25, 45, 70 °C), solvent to waste ratio (3, 6, 9), waste particle size (0.6 and 2.5 mm...

  2. Design of a solvent extraction process for PAH-contaminated sediments : The WAU-acetone process

    NARCIS (Netherlands)

    Rulkens, W.H.; Bruning, H.; Hasselt, H.J. van; Rienks, J.; Veen, H.J. van; Terlingen, J.P.M.

    1998-01-01

    Solvent extraction is one of the possibilities to clean-up polluted sediments. It is especially attractive when the sediment mainly consists of clay particles polluted with contaminants which are not, or not easily, biodegradable. Using acetone as extracting agent the extraction process has been inv

  3. Design of a solvent extraction process for PAH-contaminated sediments : The WAU-acetone process

    NARCIS (Netherlands)

    Rulkens, W.H.; Bruning, H.; Hasselt, H.J. van; Rienks, J.; Veen, H.J. van; Terlingen, J.P.M.

    1998-01-01

    Solvent extraction is one of the possibilities to clean-up polluted sediments. It is especially attractive when the sediment mainly consists of clay particles polluted with contaminants which are not, or not easily, biodegradable. Using acetone as extracting agent the extraction process has been

  4. 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.

  5. Extraction of Illegal Dyes from Red Chili Peppers with Cholinium-Based Deep Eutectic Solvents.

    Science.gov (United States)

    Zhu, Shuqiang; Liu, Dongling; Zhu, Xinyue; Su, Along; Zhang, Haixia

    2017-01-01

    Deep eutectic solvents (DESs) as a new kind of green solvents have been used to extract bioactive compounds but there are few applications in extracting chrysoidine dyes. In this study, we developed an ultrasonic-assisted extraction method with choline chloride/hydrogen bond donor (ChCl/HBD) DES for the extraction of chrysoidine G (COG), astrazon orange G (AOG), and astrazon orange R (AOR) in food samples. Some experimental parameters, such as extraction time, raw material/solvent ratio, and temperature, were evaluated and optimized as follows: the ratio of ChCl/HBD, 1 : 2 (v/v); the ratio of sample/DES, 1 : 10 (g/mL); extraction time, 20 min; extraction temperature, 50°C. Under the optimized conditions, the limits of detection (μg/mL) were 0.10 for COG and 0.06 for AOG and AOR. The relative standard deviations were in the range of 1.2-2.1%. The recoveries of the three dyes were in the range of 80.2-105.0%. By comparing with other commonly used solvents for extracting chrysoidine dyes, the advantages of DESs proved them to be potential extraction solvents for chrysoidine G, astrazon orange G, and astrazon orange R in foods.

  6. Extraction of Illegal Dyes from Red Chili Peppers with Cholinium-Based Deep Eutectic Solvents

    Directory of Open Access Journals (Sweden)

    Shuqiang Zhu

    2017-01-01

    Full Text Available Deep eutectic solvents (DESs as a new kind of green solvents have been used to extract bioactive compounds but there are few applications in extracting chrysoidine dyes. In this study, we developed an ultrasonic-assisted extraction method with choline chloride/hydrogen bond donor (ChCl/HBD DES for the extraction of chrysoidine G (COG, astrazon orange G (AOG, and astrazon orange R (AOR in food samples. Some experimental parameters, such as extraction time, raw material/solvent ratio, and temperature, were evaluated and optimized as follows: the ratio of ChCl/HBD, 1 : 2 (v/v; the ratio of sample/DES, 1 : 10 (g/mL; extraction time, 20 min; extraction temperature, 50°C. Under the optimized conditions, the limits of detection (μg/mL were 0.10 for COG and 0.06 for AOG and AOR. The relative standard deviations were in the range of 1.2–2.1%. The recoveries of the three dyes were in the range of 80.2–105.0%. By comparing with other commonly used solvents for extracting chrysoidine dyes, the advantages of DESs proved them to be potential extraction solvents for chrysoidine G, astrazon orange G, and astrazon orange R in foods.

  7. Interfacial Phenomena in Solvent Extraction and Its Influence on Process Performance

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Solvent extraction is now finding applications in a broader range of fields than the past. Many of these applications require process equipment with shorter contact times, and in some cases to the point where the traditional equilibrium stage approach is not a good model for predicting performance. In addition,feed streams are becoming lower in concentration of the solute. This means greater feed to solvent flow ratios are being used and so loss of organics as entrainment in the feed is more of a concern both economically and environmentally. These trends mean that a greater emphasis is being placed on the kinetics of extraction and stripping in models to predict performance and on formation and coalescence of drops to control entrainment. This paper reviews recent advances in the tools for investigating kinetics and coalescence in solvent extraction processes and some of the insights that are being uncovered in these fundamental processes in solvent extraction technology.

  8. Separation of nickel, cobalt and copper by solvent extraction with P204

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Nickel, cobalt and copper were separated by solvent extraction with P204. The experimental results show that [Co(NH3)6]3+ is an inert complex in extraction kinetics, therefore cobalt can be separated from nickel and copper by non-equilibrium solvent extraction. Under the conditions of temperature 25℃, contact time of two phases 10 min, phase ratio 1:1, aqueous pH 10.10 and concentration of P204 20 %, [ Co(NH3 )6 3+ is hardly extracted by P204, while the percentage extractions of nickel and copper are 79.3 % and 93.9 % respectively. Nickel and copper are separated by equi librium solvent extraction with P204. Under the conditions of temperature 25 ℃, contact time of two phases 1 min, phase ratio 1:1, equilibrium pH 4.01 and concentration of P204 20%, the separation factor of copper and nickel is 216.

  9. DBC solvent extraction of U(VI) from thiocyanate medium

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The extraction behavior of uranium(VI) from thiocyanate medium with dibenzo-18-crown-6 (DBC) in nitrobenzene and the effects of alkali cations on the extraction were investigated. The results showed that the uranium (VI) can be effectively extracted in the presence of potassium cation, uranium (VI) is extracted as complex anionic species UO2(SCN)-3, and the stoichiometry of the extracted complex is KUO2(SCN)32DBC(o).

  10. Novel biphasic separations utilising highly selective molecularly imprinted polymers as biorecognition solvent extraction agents.

    Science.gov (United States)

    Castell, Oliver K; Allender, Christopher J; Barrow, David A

    2006-10-15

    Molecularly imprinted polymers (MIPs) represent a class of artificial receptors that promise an environmentally robust alternative to naturally occurring biorecognition elements of biosensing devices and systems. However, in general, the performance of conventional MIPs in aqueous environments is poor. In the study reported here, this limitation has been addressed by the novel application of MIPs as a solvent extraction solid phase in a biphasic solvent system. This paper describes a previously unreported use of MIPs as solvent extraction reagents, their successful application to aqueous sample media and the opportunities for utilisation of this unique system in novel biosensing and separation procedures. This study demonstrates the development of a novel biphasic solvent system utilising MIP in the extracting phase to enhance both efficiency and selectivity of a simple two phase liquid extraction. Monodisperse propranolol imprinted polymer microspheres [p(divinylbenzene-co-methacrylic acid)] were prepared by precipitation polymerisation. Initially, the affinity of the polymers for (R,S)-propranolol was assessed by established techniques whereby the MIP demonstrated greater affinity for the template than did the non-imprinted control polymer (NIP). Importantly, MIP performance was also assessed using the novel dual solvent system. The depletion of (R,S)-propranolol from the aqueous phase into the polymer containing organic phase was determined. When compared to control extractions containing no polymer the presence of MIP in the extracting solvent phase resulted in an increased extraction of (R,S)-propranolol from the aqueous phase. Importantly, this extraction was significantly greater in the presence of MIP when compared to NIP. This unique principle generates opportunities for MIP based extractions and chemical enrichments in industrial applications, offering commercial, ecological and practical advantages to traditional solvent extraction techniques. The

  11. Evaluation of different solvents to extract antibacterial compounds from jalapeño peppers.

    Science.gov (United States)

    Bacon, Karleigh; Boyer, Renee; Denbow, Cynthia; O'Keefe, Sean; Neilson, Andrew; Williams, Robert

    2017-05-01

    Chili peppers (Capsicum spp.) may possess antibacterial properties and have potential to be used in foods as antimicrobial. The complete chili pepper extract should be evaluated to determine which compounds are responsible for the antimicrobial activity. Extraction of compounds from the pepper is completed using a solvent. The type of solvent used for extraction influences which compounds are isolated, therefore the best extraction method needs to be determined. The purpose of this study was to identify which solvent is most successful at extracting unknown antibacterial compounds from jalapeño peppers. Fresh jalapeño peppers were chopped, weighed, and blended with a solvent (sterilized hot water, 70% methanol, 95% methanol, 70% ethanol, or 95% ethanol) at a 1:1 ratio (g/g) until the mixture was homogenized, followed by shaking for 15 min. The slurry was centrifuged; supernatant was removed and used for antibacterial testing against Listeria monocytogenes, Escherichia coli O157:H7, and Salmonella enterica. The diameter of growth inhibition was measured and statistically evaluated using ANOVA to determine the extract with the greatest antimicrobial activity. Solvents were tested alone as a control. There was greater bacterial inhibition from extracts created with methanol and ethanol than hot water. Listeria monocytogenes was significantly more susceptible to the extracts than E. coli or Salmonella isolates. Each solvent extract was then analyzed using high-performance liquid chromatography (HPLC) and fractions (A-G) were collected and used for subsequent disk diffusion analysis against L. monocytogenes. Fractions E and F (eluded between 20 and 30 min) exhibited the most antibacterial activity. There were no differences between solvents used (p = .05). Further investigation into specific compounds within these extracts will be completed in the future.

  12. Effect of solvent and extraction time on the antioxidant properties of Citrus macroptera

    OpenAIRE

    2014-01-01

    We aimed to evaluate the effects of solvents and different time intervals on the extractions of phenolic compounds and antioxidant properties of the pulp of the Citrus macroptera. The pulp of the fruit was extracted for one and two hours separately with four types of solvent namely- methanol, ethanol, acetone and water. Total phenolic content was determined by using Folin-Ceucalteu method, while ferric reducing antioxidant power (FRAP), total antioxidant capacity (TAC), 1,1- diphenyl-2-picryl...

  13. A comparative study of solvent and supercritical CO2 extraction of Simarouba gluaca seed oil

    Directory of Open Access Journals (Sweden)

    B. Anjaneyulu

    2017-09-01

    Full Text Available In the present study, the supercritical carbon dioxide (CO2 extraction of oil from Simarouba gluaca seeds was carried out at varying conditions of pressure (300–500 bar, temperature (50–70 °C and CO2 flow rate (10–30 g·min-1. The extraction condition for maximum oil yield was obtained at 500 bar pressure, 70 °C and at 30 g·min-1 flow rate of CO2. The extracted oil was analyzed thoroughly for physico-chemical properties and compared with those of conventional solvent extracted oil. An interesting observation is a significant reduction in the phosphorus content of the oil (8.4 mg·kg-1 extracted using supercritical CO2 compared to the phosphorous content of the solvent extracted oil (97 mg·kg-1. Moreover, the content of total tocopherols in supercritically extracted oil (135.6 mg·kg-1 was found to be higher than the solvent extracted oil (111 mg·kg-1. The rest of the physico-chemical properties of the two differently extracted oils matched well with each other. The results indicated the possible benefits of supercritical CO2 extraction over solvent extraction of Simarouba gluaca seed oil.

  14. Extraction of orange peel's essential oil by solvent-free microwave extraction

    Science.gov (United States)

    Qadariyah, Lailatul; Amelia, Prilia Dwi; Admiralia, Cininta; Bhuana, Donny S.; Mahfud, Mahfud

    2017-05-01

    Sweet orange peel (Citrus sinensis) is part of orange plant that contains essential oils. Generally, taking essential oil from orange peel is still using hydrodistillation and steam-hydrodistillation method which still needs solvent and takes a long time to produce high quality essential oil. Therefore, the objectives of this experiment are to study the process of orange peel's essential oil extraction using Solvent Free Microwave Extraction (SFME) and to study the operating condition that effect an optimum yield and quality of the essential oil. In this experiment, extraction process with SFME method goes for 60 minutes at atmospheric pressure. Variables for SFME are: variation of orange peel condition (fresh and dry), ratio orange peel mass to distiller volume (0,1; 0,2; 0,3; 0,4 g/mL), orange peel size (±0,5; ±2; ±3,5 cm width), and microwave power (100, 264, 400 Watt). Moisture content of fresh peel is 71,4% and for dry peel is 17,37% which is obtained by sun drying. The result of this experiment will be analyzed with GC-MS, SEM, density, and miscibility in ethanol 90%. The optimum result obtained from this experiment based on the number of the yield under condition of fresh orange peel is at peel mass/distiller volume 0,1 g/mL, orange peel size ±3,5 cm width, and microwave power 400 Watt, results 1,6738% yield. The result of GC-MS for fresh orange peel shows that the dominant compound is Limonene 54,140% and for dry orange peel is Limonene 59,705%. The density obtained is around 0,8282-0,8530 g/mL and miscibility in ethanol 90% is 1:5.

  15. Reactive Extraction of L (+ Tartaric Acid by Amberlite LA-2 in Different Solvents

    Directory of Open Access Journals (Sweden)

    I. Inci

    2011-01-01

    Full Text Available The extraction of L(+ tartaric acid from aqueous solutions by amberlite LA-2 is a secondary amine mixture in different diluent solvents. Extraction equilibria of L(+ tartaric acid by amberlite LA-2 in 1-octanol, cyclohexane, isooctane, hexane, methyl isobutyl ketone (MIBK solvents at temperature 298.15 K have been measured. The batch extraction experiments distribution coefficients (D, loading factors ( Z and extraction efficiency (E were calculated. The maximum removal of L(+ tartaric acid is 91 % with MIBK and 0.92 mol.L-1 initial concentration of Amberlite LA-2.

  16. SOLVENT EFFECT ON EXTRACTION OF GALLIC ACID FROM AMALAKI CHURNA (EMBLICA OFFICINALIS Gaertn. TO REDUCE MATRIX EFFECT USING HPTLC AND UV-SPECTROSCOPY WITH 12 DIFFERENT NATURE SOLVENTS

    Directory of Open Access Journals (Sweden)

    Sukla V.J.

    2012-06-01

    Full Text Available Standardization of Ayurvedic formulations is an important aspect for research in Indian medicine. In this era every Pharma company prefer to use pure extract of component for production of best product in short period of time. The literature survey reveals that no work has been reported for solvent selection of extraction of Ayurvedic drugs. Amalaki is one of the most useable ayurveda drug. So, the present study was selected with an aim to select solvent for extraction of component of interest. Standard for evaluating quality of Amalaki churna by employing various physico-chemical parameters. For solvent selection 12 different nature solvents are selected for extraction. Polar solvent selected are Water, Di methylsulfoxide (DMSO, Ethylene glycol, Acetonitrile, Di methyl formeamide (DMF and Methanol. Non polar solvents are Acetone, Acetic acid, Ethyl acetate, Chloroform, Di ethylether and Toluene. Extraction was done by maceration method. Results are taken by chromatographic and spectrophotometric methods. In observation component was easily extracted with less interfering component in non polar solvent. Gallic acid is component of interest for Amalaki and it is well extracted in Di ethyl ether as per result of chromatography and spectroscopy. Conclusion is that selection of solvent for extraction as per their component of interest from material.

  17. Environmental life cycle assessment on the separation of rare earth oxides through solvent extraction.

    Science.gov (United States)

    Vahidi, Ehsan; Zhao, Fu

    2017-12-01

    Over the past decade, Rare Earth Elements (REEs) have gained special interests due to their significance in many industrial applications, especially those related to clean energy. While REEs production is known to cause damage to the ecosystem, only a handful of Life Cycle Assessment (LCA) investigations have been conducted in recent years, mainly due to lack of data and information. This is especially true for the solvent extraction separation of REEs from aqueous solution which is a challenging step in the REEs production route. In the current investigation, an LCA is carried out on a typical REE solvent extraction process using P204/kerosene and the energy/material flows and emissions data were collected from two different solvent extraction facilities in Inner Mongolia and Fujian provinces in China. In order to develop life cycle inventories, Ecoinvent 3 and SimaPro 8 software together with energy/mass stoichiometry and balance were utilized. TRACI and ILCD were applied as impact assessment tools and LCA outcomes were employed to examine and determine ecological burdens of the REEs solvent extraction operation. Based on the results, in comparison with the production of generic organic solvent in the Ecoinvent dataset, P204 production has greater burdens on all TRACI impact categories. However, due to the small amount of consumption, the contribution of P204 remains minimal. Additionally, sodium hydroxide and hydrochloric acid are the two impactful chemicals on most environmental categories used in the solvent extraction operation. On average, the solvent extraction step accounts for 30% of the total environmental impacts associated with individual REOs. Finally, opportunities and challenges for an enhanced environmental performance of the REEs solvent extraction operation were investigated. Copyright © 2017 Elsevier Ltd. All rights reserved.

  18. 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.

  19. Exploiting Sequential Injection on-line Solvent Extraction/Back Extraction with Detection by ETAAS or ICPMS

    DEFF Research Database (Denmark)

    Wang, Jianhua; Hansen, Elo Harald

    tolerances. With detection by ETAAS, separation/preconcentration by solvent extraction has enjoyed much use. However, this approach is not necessarily the optimal one since introduction of organic eluates directly into the graphite tube might lead to deteriorated reproducibility and lower sensitivity....... And for ICPMS, organics are prohibitive because they give rise to an unstable plasma, and excessive carbon deposited on the sampling and skimmer cones might result in a gradual loss of sensitivity. All of these difficulties can be readily overcome by using solvent extraction/back extraction. Surprisingly...

  20. Exploiting sequential injection on-line solvent extraction/back extraction with detection by ETAAS and ICPMS

    DEFF Research Database (Denmark)

    Wang, Jianhua; Hansen, Elo Harald

    . With detection by ETAAS, separation/preconcentration by solvent extraction has enjoyed much use. However, this approach is not necessarily the optimal one since introduction of organic eluates directly into the graphite tube might lead to deteriorated reproducibility and lower sensitivity. And for ICPMS......, organics are prohibitive because they give rise to an unstable plasma, and excessive carbon deposited on the sampling and skimmer cones might result in a gradual loss of sensitivity. All of these difficulties can be readily overcome by using solvent extraction/back extraction. Surprisingly, this approach...

  1. Chemical profiling of Curcuma aeruginosa Roxb. rhizome using different techniques of solvent extraction

    Directory of Open Access Journals (Sweden)

    Sanimah Simoh

    2015-05-01

    Conclusions: It was evident from the results that C. aeruginosa rhizome extracted using two different techniques of solvent extractions (MTBE and M/C contained various chemical classes of compounds including terpenoids, sterols, organic acids, fatty acids and sugars. Different methods of extraction have led to different compounds extraction for C. aeruginosa rhizome. The results also indicated that the plant was a source of phytochemical importance.

  2. Extraction of coal with solvents in liquid and supercritical state under nonhydrogenating and hydrogenating conditions

    Science.gov (United States)

    Wilhelm, A.; Hedden, K.

    1982-10-01

    The basic steps of coal extraction to determine the optimum conditions for obtaining a higher coal conversion yield in a technical process of supercritical coal extraction were examined. A fixed bed of coal was slowly heated up in a current of pressurized solvent by a nonisothermal technique. The solvent changes its physical state during extraction from a liquid to a supercritical fluid. The formation rates of extract and gaseous products and their integral yields were measured under different extraction conditions. Various coals and lignites as well as different solvents including H-donor solvents and the effect of the addition of molecular hydrogen to the supercritical phase with and without catalyst were studied. Results are interpreted with an extraction scheme, comprising chemical reactions, phase equilibria and transport processes as single steps of the complex extraction procedure. Using a simplified mathematical model, the formation rates of extract as a function of temperature were quantitatively described with effective kinetic parameters. New process for the hydrogenating supercritical extraction of coal, which produces high coal conversion yields is proposed.

  3. Energy compensation of slow extracted beams with RF acceleration

    Science.gov (United States)

    Fujimoto, Tetsuya; Souda, Hikaru; Torikoshi, Masami; Kanai, Tatsuaki; Yamada, Satoru; Noda, Koji

    2016-03-01

    In a conventional carbon-ion radiotherapy facility, a carbon-ion beam is typically accelerated up to an optimum energy, slowly extracted from a synchrotron ring by a resonant slow extraction method, and ultimately delivered to a patient through a beam-delivery system. At Japan's Gunma University, a method employing slow-beam extraction along with beam-acceleration has been adopted. This method slightly alters the extracted-beam's energy owing to the acceleration component of the process, which subsequently results in a residual-range variation of approximately 2 mm in water-equivalent length. However, this range variation does not disturb a distal dose distribution with broad-beam methods such as the single beam-wobbling method. With the pencil-beam 3D scanning method, however, such a range variation disturbs a distal dose distribution because the variation is comparable to slice thickness. Therefore, for pencil-beam 3D scanning, an energy compensation method for a slow extracted beam is proposed in this paper. This method can compensate for the aforementioned energy variances by controlling net energy losses through a rotatable energy absorber set fixed between the synchrotron exit channel and the isocenter. Experimental results demonstrate that beam energies can be maintained constant, as originally hypothesized. Moreover, energy-absorber positions were found to be significantly enhanced by optimizing beam optics for reducing beam-size growth by implementation of the multiple-scattering effect option.

  4. A green deep eutectic solvent-based aqueous two-phase system for protein extracting

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Kaijia; Wang, Yuzhi, E-mail: wyzss@hnu.edu.cn; Huang, Yanhua; Li, Na; Wen, Qian

    2015-03-15

    Highlights: • A strategy for the protein purification with a deep eutectic solvent(DES)-based aqueous two-phase system. • Choline chloride-glycerin DES was selected as the extraction solvent. • Bovine serum albumin and trypsin were used as the analytes. • Aggregation phenomenon was detected in the mechanism research. - Abstract: As a new type of green solvent, deep eutectic solvent (DES) has been applied for the extraction of proteins with an aqueous two-phase system (ATPS) in this work. Four kinds of choline chloride (ChCl)-based DESs were synthesized to extract bovine serum albumin (BSA), and ChCl-glycerol was selected as the suitable extraction solvent. Single factor experiments have been done to investigate the effects of the extraction process, including the amount of DES, the concentration of salt, the mass of protein, the shaking time, the temperature and PH value. Experimental results show 98.16% of the BSA could be extracted into the DES-rich phase in a single-step extraction under the optimized conditions. A high extraction efficiency of 94.36% was achieved, while the conditions were applied to the extraction of trypsin (Try). Precision, repeatability and stability experiments were studied and the relative standard deviations (RSD) of the extraction efficiency were 0.4246% (n = 3), 1.6057% (n = 3) and 1.6132% (n = 3), respectively. Conformation of BSA was not changed during the extraction process according to the investigation of UV–vis spectra, FT-IR spectra and CD spectra of BSA. The conductivity, dynamic light scattering (DLS) and transmission electron microscopy (TEM) were used to explore the mechanism of the extraction. It turned out that the formation of DES–protein aggregates play a significant role in the separation process. All the results suggest that ChCl-based DES-ATPS are supposed to have the potential to provide new possibilities in the separation of proteins.

  5. Antibacterial activity of sequentially extracted organic solvent extracts of fruits, flowers and leaves of Lawsonia inermis L. from Jaffna.

    Science.gov (United States)

    Jeyaseelan, E Christy; Jenothiny, S; Pathmanathan, M K; Jeyadevan, J P

    2012-10-01

    To reveal the antibacterial activity of sequentially extracted different cold organic solvent extracts of fruits, flowers and leaves of Lawsonia inermis (L. against) some pathogenic bacteria. Powders of fruits, flowers and leaves of L. inermis were continuously extracted with dichloromethane (DCM), ethyl acetate and ethanol at ambient temperature. The dried extracts were prepared into different concentrations and tested for antibacterial activity by agar well diffusion method, and also the extracts were tested to determine the available phytochemicals. Except DCM extract of flower all other test extracts revealed inhibitory effect on all tested bacteria and their inhibitory effect differed significantly (Peffect was showed by ethyl acetate extract of flower against Staphylococcus aureus (S. aureus) and Pseudomonas aeruginosa (P. aeruginosa), and ethyl acetate extract of fruit on Escherichia coli (E. coli) and Bacillus subtilis (B. subtilis). The ethyl acetate and ethanol extracts of flower, fruit and leaf expressed inhibition even at 1 mg/100 µl against all test bacteria. Among the tested phytochemicals flavonoids were detected in all test extracts except DCM extract of flower. The study demonstrated that the ethyl acetate and ethanol extracts of fruit and flower of L. inermis are potentially better source of antibacterial agents compared to leaf extracts of respective solvents.

  6. Antibacterial activity of sequentially extracted organic solvent extracts of fruits, flowers and leaves of Lawsonia inermis L. from Jaffna

    Institute of Scientific and Technical Information of China (English)

    E Christy Jeyaseelan; S Jenothiny; MK Pathmanathan; JP Jeyadevan

    2012-01-01

    To reveal the antibacterial activity of sequentially extracted different cold organic solvent extracts of fruits, flowers and leaves of Lawsonia inermis (L. against) some pathogenic bacteria. Methods: Powders of fruits, flowers and leaves of L. inermis were continuously extracted with dichloromethane (DCM), ethyl acetate and ethanol at ambient temperature. The dried extracts were prepared into different concentrations and tested for antibacterial activity by agar well diffusion method, and also the extracts were tested to determine the available phytochemicals.Results:Except DCM extract of flower all other test extracts revealed inhibitory effect on all tested bacteria and their inhibitory effect differed significantly (P<0.05). The highest inhibitory effect was showed by ethyl acetate extract of flower against Staphylococcus aureus (S. aureus) and Pseudomonas aeruginosa (P. aeruginosa), and ethyl acetate extract of fruit on Escherichia coli (E. coli) and Bacillus subtilis (B. subtilis). The ethyl acetate and ethanol extracts of flower, fruit and leaf expressed inhibition even at 1 mg/ 100 μl against all test bacteria. Among the tested phytochemicals flavonoids were detected in all test extracts except DCM extract of flower.Conclusions:The study demonstrated that the ethyl acetate and ethanol extracts of fruit and flower of L. inermis are potentially better source of antibacterial agents compared to leaf extracts of respective solvents.

  7. Effects of extraction solvent on fucose content in fucoidan extracted from brown seaweed (Sargassum sp.) from Pulau Langkawi, Kedah, Malaysia

    Science.gov (United States)

    Baba, Bibi Marliana; Mustapha, Wan Aida Wan; Joe, Lim Seng

    2016-11-01

    The objective of this study was to determine the effects of extraction solvent on the fucose content in fucoidan that had been isolated from Sargassum sp., which is a type of brown seaweed that was harvested in Pulau Langkawi, Kedah, Malaysia. There were three different solvents that were used in the extraction process in order to isolate the crude fucoidan including the hydrochloric acid, HCl, calcium chloride, CaCl2 solution and also the papain ezyme solution. Other extraction parameters that were the extraction temperature and time were fixed at three hours, at 45°C respectively. It was found that there was a significant different (p 0.05) amongst each other. Hence, this study indicated that the extraction of fucoidan using HCl tend to possess higher fucose content which will increase the potential of the extraction method to be used in the industries such as pharmaceuticals as well as the nutraceuticals.

  8. Green extraction of glycosides from Stevia rebaudiana (Bert. with low solvent consumption: A desirability approach

    Directory of Open Access Journals (Sweden)

    Paula M. Martins

    2016-12-01

    Full Text Available The sweet flavor of Stevia rebaudiana (Bert. leaf extract is well known and has raised the interest of huge food companies due to its natural bid. The extraction of their main glycosides stevioside and rebaudioside A is an important step on the preparation of final Stevia granules. The aim of the work reported here was to study and optimize the dynamic maceration of Stevia leaves using water and ethanol as green solvents. For instance, a fractional factorial design was chosen to evaluate the individual effects of the drug powder size, weight ratio of drug to solvent, temperature, agitation, and time on the yield of these glycosides. The glycosides were quantified by high pressure liquid chromatography. An exhaustive extraction by successive maceration steps showed that ethanol 70% was superior to water and ethanol 90% for stevioside and rebaudioside extraction. The liquid extract composition in dry basis and the yield of stevioside and rebaudioside A were significantly affected by the drug to solvent weight ratio, showing that larger volumes of solvent should be used. Furthermore, increasing solvent volume favors the extraction of the stevioside by a twofold factor as compared to rebaudioside A. Among the other factors, only drug powder size affected the yield of rebaudioside A significantly. The optimal solution for S. rebaudiana leaves dynamic extraction estimated by desirability functions methodology led to a condition which allows obtaining extraction yields of 2.31 and 1.24% for stevioside and rebaudioside A and their concentrations in dried extract corresponding to 8.38 and 4.51%, respectively. These high yields were obtained with drug to solvent ratio (1:10, w/w much higher than previous works, thus resulting in a more sustainable and green process.

  9. Sample Results From The Extraction, Scrub, And Strip Test For The Blended NGS Solvent

    Energy Technology Data Exchange (ETDEWEB)

    Washington, A. L. II; Peters, T. B.

    2014-03-03

    This report summarizes the results of the extraction, scrub, and strip testing for the September 2013 sampling of the Next Generation Solvent (NGS) Blended solvent from the Modular Caustic Side-Solvent Extraction Unit (MCU) Solvent Hold Tank. MCU is in the process of transitioning from the BOBCalixC6 solvent to the NGS Blend solvent. As part of that transition, MCU has intentionally created a blended solvent to be processed using the Salt Batch program. This sample represents the first sample received from that blended solvent. There were two ESS tests performed where NGS blended solvent performance was assessed using either the Tank 21 material utilized in the Salt Batch 7 analyses or a simulant waste material used in the V-5/V-10 contactor testing. This report tabulates the temperature corrected cesium distribution, or DCs values, step recovery percentage, and actual temperatures recorded during the experiment. This report also identifies the sample receipt date, preparation method, and analysis performed in the accumulation of the listed values. The calculated extraction DCs values using the Tank 21H material and simulant are 59.4 and 53.8, respectively. The DCs values for two scrub and three strip processes for the Tank 21 material are 4.58, 2.91, 0.00184, 0.0252, and 0.00575, respectively. The D-values for two scrub and three strip processes for the simulant are 3.47, 2.18, 0.00468, 0.00057, and 0.00572, respectively. These values are similar to previous measurements of Salt Batch 7 feed with lab-prepared blended solvent. These numbers are considered compatible to allow simulant testing to be completed in place of actual waste due to the limited availability of feed material.

  10. SOLVENT EXTRACTION PROCESS FOR SEPARATING ACTINIDE AND LANTHANIDE METAL VALUES

    Science.gov (United States)

    Hildebrandt, R.A.; Hyman, H.H.; Vogler, S.

    1962-08-14

    A process of countercurrently extracting an aqueous mineral acid feed solution for the separation of actinides from lanthanides dissolved therern is described. The feed solution is made acid-defrcient with alkali metal hydroxide prior to.contact with acid extractant; during extraction, however, acid is transferred from organic to aqueous solution and the aqueous solution gradually becomes acid. The acid-deficient phase ' of the process promotes the extraction of the actinides, while the latter acid phase'' of the process improves retention of the lanthanides in the aqueous solution. This provides for an improved separation. (AEC)

  11. Solvent-solvent fractionations of Combretum erythrophyllum (Burch.) leave extract: Studies of their antibacterial, antifungal, antioxidant and cytotoxicity potentials

    Institute of Scientific and Technical Information of China (English)

    Fanyana M. Mtunzi; Ikechukwu P. Ejidike; Imelda Ledwaba; Aroke Ahmed; Vusumzi E. Pakade; Michael J. Klink; Sekomeng J. Modise

    2017-01-01

    Objective: To evaluate the biological activities of Combretum erythrophyllum (C. erythrophyllum) leaf extracts against infectious diseases' pathogenesis and their cytotoxicity potentials. Methods: Powdered leaf material (300 g) of C. erythrophyllum was extracted (1:10 w/v) using acetone to obtain the crude extract. Liquid-liquid fractionation was performed on the crude acetone extract (30 g) using solvents of different polarity. The bioautographic method was used to detect the inhibition of bacterial and fungal growth by active compounds present in the crude and fractions. The extracts were then tested on bacterial strains: Staphylococcus aureus, Enterococcus faecalis, Escherichia coli, Pseudomonas aeruginosa; fungal strains: Candida albicans (C. albicans), Cryptococcus neoformans, and Aspergillus fumigatus, by microtitre dilution method for MIC determination. Results: The extracts MIC values ranged between 0.08–2.50 mg/mL against the tested pathogens. Water fraction had the highest activity against bacteria strains, while the fungal assay revealed crude acetone extract and ethyl acetate fraction to be active against C. albicans (1.25 mg/mL), dichloromethane extract against C. albicans and Aspergillus fumigatus (0.16 mg/mL). Extract fractions showed a good antioxidant activity via DPPH, ABTS and hydroxyl radical scavenging assays, in the order: ethyl acetate > water >acetone > dichloromethane > hexane. The toxicity level of crude extract and fractions evaluated in Vero monkey kidney cells ranged from 34–223 μg/mL, while doxorubicin (IC50 = 7.19 μg/mL) served as the positive control. Conclusions: It can be concluded that the extracts of C. erythrophyllum are safe for medicinal use in folk medicine for treating infectious and stress related diseases.

  12. Influence of solvents on extraction of U(Ⅵ) by N,N'-didecanoylpiperazine

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Extraction behavior of N, N'-didecanoylpiperazine (DDPEZ) for U(Ⅵ)in a series of solvents from aqueous nitric acid media was investigated for the first time.The dependence of distribution ratios on the concentration of aqueous nitric acid.extractant and temperature has been discussed. The increasing sequence of extractiveability of DDPEZ is given: chloroform, carbon tetrachloride, dimethylbenzene, toluene,benzene.``

  13. Opportunities for switchable solvents for lipid extraction from wet algal biomass: an energy evaluation

    NARCIS (Netherlands)

    Du, Ying; Schuur, Boelo; Kersten, Sascha R.A.; Brilman, Derk Willem Frederik

    2015-01-01

    Algae are considered an important sustainable feedstock for lipid extraction to produce food ingredients, cosmetics, pharmaceutical products and biofuels. Next to the costs for cultivation, this route is especially hindered by the energy intensity of drying algae prior to extraction and solvent

  14. Anticomplement activity of organic solvent extracts from Korea local Amarantaceae spp.

    Science.gov (United States)

    Jung, Seil; Lee, Jai-Heon; Lee, Young-Choon; Moon, Hyung-In

    2012-04-01

    The study evaluated the anticomplement activity from various solvent extracts of nine Amarantaceae plants (Achyranthes japonica (Miq.) Nakai, Amaranthus mangostanus L., Amaranthus retroflexus L., Amaranthus spinosus L., Celosia argentea var. spicata., Amaranthus lividus L., Celosia cristata L., Amaranthus viridis L., Gomphrena globosa L.) from South Korea on the classical pathway. We have evaluated various organic solvent extract from nine Amarantaceae plants with regard to its anticomplement activity on the classical pathway. Achyranthes japonica chloroform extracts showed inhibitory activity against complement system with 50% inhibitory concentrations (IC(50)) value of 73.1μg/ml. This is the first report of anticomplement activity from Amarantaceae plants.

  15. Chetoui olive leaf extracts: influence of the solvent type on the phenolics and antioxidant activities

    Energy Technology Data Exchange (ETDEWEB)

    Abaza, L.; Ben Youssef, N.; Manai, H.; Haddada, F.M.; Methenni, K.; Zarrouk, M.

    2011-07-01

    The aim of this study was to investigate the influence of the solvent type on the extraction of phenolics and the antioxidant properties of the extracts obtained from Chetoui olive leaves. Extraction was conducted at room temperature using four solvents: deionized water (ddH2O), 80% methanol (80% MeOH), 70% ethanol (70% EtOH), and 80% acetone. Total phenols and total flavonoids were measured using the Folin-Ciocalteau and aluminum chloride colorimetric methods, respectively. The antioxidant properties have been determined by two scavenging activity methods, DPPH and ABTS. (Author).

  16. Energy requirements for wet solvent extraction of lipids from microalgal biomass.

    Science.gov (United States)

    Martin, Gregory J O

    2016-04-01

    Biofuel production from microalgae requires energy efficient processes for extracting and converting triacylglyceride lipids to fuel, compatible with coproduction of protein feeds and nutraceuticals. Wet solvent extraction involves mechanical cell rupture, lipid extraction via solvent contacting, physical phase separation, thermal solvent recovery, and transesterification. A detailed analysis of the effect of key process parameters on the parasitic energy demand of this process was performed. On a well-to-pump basis, between 16% and 320% of the resultant biodiesel energy was consumed depending solely on the process parameters. Highly positive energy balances can be achieved, but only if a correctly designed process is used. This requires processing concentrated biomass (ca 25%w/w) with a high triacylglyceride content (ca 30%w/w), and an efficient extraction process employing a non-polar solvent, low solvent-to-paste ratio, and efficient energy recovery. These requirements preclude many laboratory scale processes and polar co-solvents as viable options for large-scale biofuel production. Copyright © 2016 Elsevier Ltd. All rights reserved.

  17. Recovery of zinc from low-grade zinc oxide ores by solvent extraction

    Institute of Scientific and Technical Information of China (English)

    覃文庆; 蓝卓越; 黎维中

    2003-01-01

    The recovery of zinc from low-grade zinc oxide ores with solvent extraction-electrowinning technique was investigated by using D2EHPA as extractant and 260# kerosene as diluent. The results show that it is possible to selectively leach zinc from the ores by heap leaching. The zinc concentration of leach solution in the first leaching cycle is 32.57 g/L, and in the sixteenth cycle the zinc concentration is 8.27g/L after solvent extraction. The leaching solution is subjected to solvent extraction, scrubbing and selective stripping for enrichment of zinc and removal of impurities. The pregnant zinc sulfate solution produced from the stripping cycle is suitable for zinc electrowinning.Extra-pure zinc metal was obtained in the electrowinning test under conventional conditions.

  18. Effect of dietary substitution with solvent extracted neem seed cake ...

    African Journals Online (AJOL)

    STORAGESEVER

    2009-07-06

    Jul 6, 2009 ... Extraction of the residual bitter component (neem seed cake alcoholic extract) ... for 6 h as described by modified method of Mitra (1963) to remove ... Daily feed intake was measured, as decrease in the quantity of weighed ...

  19. Solvent extraction of vanadium from sulfuric acid solution

    Institute of Scientific and Technical Information of China (English)

    WANG Mingyu; ZHANG Guiqing; WANG Xuewen; ZHANG Jialiang

    2009-01-01

    The behaviour of vanadium(V) extracted from sulfuric acid solution was investigated using Cyanex 923 as an cxtractant. The effects of the concentration of Cyanex 923 and the pH of the solution were studied. The extraction of vanadium(V) increases with the increase of Cyanex 923 concentration and shaking time. Cyanex 923 can extract vanadium(V) fi'om sulfuric acid solution at low pH conditions, and the best pH conditions for exuaction of vanadium(V) are at pH 1.0-2.0. The species extracted into the organic phase is VO2HSO4 with one molecule of Cyanex 923. Equilibrium studies were used to assess the extraction efficiency of vanadium(V) recovery from the sulfuric acid solution.

  20. 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.

  1. Turn-By Beam Extraction during Acceleration in a Synchrotron

    Science.gov (United States)

    Tsoupas, Nicholaos; Trbojevic, Dejan

    2014-02-01

    A synchrotron to accelerate protons or carbon ions for medical applications is being designed at Brookhaven National Laboratory (BNL). Single beam bunches with maximum beam energy of 1.18 GeV and 400 MeV/u for protons and carbon ions respectively will be extracted from the synchrotron at 15 Hz. For protons, the maximum required energy for irradiating a tumor is ˜206 MeV. A pencil-like proton beam containing ˜5.4×107 p/bunch delivers a therapeutic dose of 2.5 Gy in ˜1.5 minutes to treat a tumor of 1 liter volume. It will take ˜80 minutes with bunches containing 4.5×104 ions/bunch to deliver the same dose of 2.5 Gy with a 400 MeV/u pencil-like carbon beam. This extended treatment time when using carbon ions is not acceptable. In addition, the synchrotron cannot be controlled with a beam bunch containing such a low number of carbon ions. To overcome these two problems of the extended treatment time and the low bunch intensity required for the treatment when carbon ions are used, we have devised a method to “peel” the required 4.5×104 carbon-ions/bunch from the accelerating carbon beam bunch containing ˜108 ions/bunch and deliver them to the tumor on a “turn-by-turn” basis. Unlike other methods of beam extraction from a synchrotron, such as resonance extraction, this method does not allow for any beam losses during the extraction and the carbon beam can be peeled off in less than 15 ms during the acceleration or deceleration cycle of the synchrotron. Thus, this turn-by-turn beam extraction method provides beam with variable energy and precisely controlled beam current during the 30 ms acceleration or deceleration time.

  2. NEXT GENERATION SOLVENT-MATERIALS COMPATIBILITY WITH POLYMER COMPONENTS WITHIN MODULAR CAUSTIC-SIDE SOLVENT EXTRACTION UNIT (FINAL REPORT)

    Energy Technology Data Exchange (ETDEWEB)

    Fondeur, F.; Peters, T.; Fink, S.

    2012-01-17

    The Office of Waste Processing, within the Office of Technology Innovation and Development, is funding the development of an enhanced solvent for deployment at the Savannah River Site for removal of cesium from High Level Waste. The technical effort is collaboration between Oak Ridge National Laboratory (ORNL), Savannah River National Laboratory (SRNL), and Argonne National Laboratory. The first deployment target for the technology is within the Modular Caustic-Side Solvent Extraction Unit (MCU). Deployment of a new chemical within an existing facility requires verification that the chemical components are compatible with the installed equipment. In the instance of a new organic solvent, the primary focus is on compatibility of the solvent with organic polymers used in the facility. This report provides the data from exposing these polymers to the Next Generation Solvent (NGS). The test was conducted over six months. An assessment of the dimensional stability of polymers present in MCU (i.e., PEEK, Grafoil, Tefzel and Isolast) in the modified NGS (where the concentration of LIX{reg_sign}79 and MaxCalix was varied systematically) showed that LIX{reg_sign}79 selectively affected Tefzel and its different grades (by an increase in size and lowering its density). The copolymer structure of Tefzel and possibly its porosity allows for the easier diffusion of LIX{reg_sign}79. Tefzel is used as the seat material in some of the valves at MCU. Long term exposure to LIX{reg_sign}79, may make the valves hard to operate over time due to the seat material (Tefzel) increasing in size. However, since the physical changes of Tefzel in the improved solvent are comparable to the changes in the CSSX baseline solvent, no design changes are needed with respect to the Tefzel seating material. PEEK, Grafoil and Isolast were not affected by LIX{reg_sign}79 and MaxCalix within six months of exposure. The initial rapid weight gain observed in every polymer is assigned to the finite and

  3. Effectivity of Beta vulgaris L. Extract with various Solvent Fractions to Aedes aegypti Larval Mortality

    Directory of Open Access Journals (Sweden)

    Mutiara Widawati

    2013-06-01

    Full Text Available Dengue vector control is mostly done by using plant-based insecticides. Insecticides from the vegetable and fruit extracts of the leaves of plants that contain compounds alkaloids, saponins, flavonoids, tannins, triterpenoids, and polyphenols can be used as an alternative to naturally control Ae. aegypti. The purpose of this study was to determine the effectiveness of the B. vulgaris L. extract larvacide against larvae of Ae. aegypti. The materials that been used was B. vulgaris L. fruit parts which was milled and dried to become a powder form. 800 g of dry powder was extracted by 70% methanol by percolation method with occasional stirring for 3 days. The extract was concentrated using an evaporator. 60 g remaining residue was dissolved in distilled water and re-extracted with diethyl ether, chloroform, and ethyl acetate. Each fraction extract was dried with anhydrous sodium sulfate and the solvent was distilled. The extract was tested qualitatively to determine the content of secondary metabolites. Larvacide test performed by dissolving each extracts in dimetilsulphoxide (DMSO at concentrations of 0.1, 0.5 and 1%. The larvae used was larval of Ae. aegypti age of seven days. Death larvae counted every day for seven days to determine the effect of the contact. Tests carried out at a temperature of 27±1°C by immersing 25 larvae at each concentration of the extract with 50 mL volume and three replications was performed. The data obtained were analyzed further with different test. The results showed that fruit extract contains flavonoids, alkoloid, sterols, triterpenes, saponins and tannins. Highest mortality happened which was 82.5% and the lowest mortality happened with a concentration of 0.1% diethyl ether extract fraction. The extracts that are dissolved in various solvent fractions have not been effective as a larvacide until the highest concentration which was 1%. Methanol and polar solvent extracts of the fruit has a larvacide potency a bit

  4. Options for the recovery of cerium by solvent extraction

    Energy Technology Data Exchange (ETDEWEB)

    Soldenhoff, K.H. [Australian Nuclear Science and Technology Organisation, Lucas Heights, NSW (Australia)

    1996-12-31

    This paper reports the results of an experimental program to examine the use of various commercial reagents for the extraction of cerium (IV) from sulphate solutions. Extractants tested include organophosphorus esters (TOPO, Cyanex 923 and Cyanex 925), organophosphorus acids (DEHPA, lonquest 801 and Cyanex 272) and high molecular weight amine, Alamine 336. The suitability of reagents is assessed in terms of process relevant criteria such as extraction dependence on acidity, selectivity over other rare earths and thorium, stability of reagent towards oxidation and loading characteristics. (author) 15 refs., 2 tabs., 5 figs.

  5. POLY(AMINOMETHYLENEPHOSPHONIC ACID FOR SOLVENT EXTRACTION OF METAL IONS

    Directory of Open Access Journals (Sweden)

    M’hamed Kaid

    2011-09-01

    Full Text Available Diaminododecyltetramethylenetetraphosphonic acid (DADTMTPA has been investigated in liquid - liquid extraction of Zn (II and Cu (II in acetate media. The extraction of both cations was carried out in different media with the addition of CH3COONa, CH3COOH, HCl and H2SO4 at different pH values. The maximum extraction yield for copper is 70% after addition of 10 mg of sodium acetate and for zinc is 30% after addition of acetic acid at pHi = 5.5, in one step.

  6. Improved dissolution of Kaempferia parviflora extract for oral administration by preparing solid dispersion via solvent evaporation

    Directory of Open Access Journals (Sweden)

    Yotsanan Weerapol

    2017-03-01

    Full Text Available Kaempferia parviflora, a plant in the family Zingiberaceae, has been used in Thai traditional medicines for treating hypertension and promoting longevity with good health and well-being. However, its limited aqueous solubility and low dissolution restrict its bioavailability. The aim of the study was therefore to improve the dissolution rate of K. parviflora extracted with dichloromethane (KPD by solid dispersions. Different water-soluble polymers were applied to improve dissolution of KPD. The solid dispersions in different ratios were prepared by solvent evaporation method. Only hydroxypropyl methylcellulose (HPMC and polyvinyl alcohol-polyethylene glycol grafted copolymer (PVA-co-PEG could be used to produce homogeneous, powdered solid dispersions. Physical characterization by scanning electron microscopy, hot stage microscopy, differential scanning calorimetry and powder X-ray diffractometry, in comparison with corresponding physical mixtures, showed the changes in solid state during the formation of solid dispersions. Dissolution of a selected marker, 5,7,4′-trimethoxyflavone (TMF, from KPD/HPMC and KPD/PVA-co-PEG solid dispersions was significantly improved, compared with pure KPD. The dissolution enhancement by solid dispersion was influenced by both type and content of polymers. The stability of KPD/HPMC and KPD/PVA-co-PEG solid dispersions was also good after 6-month storage in both long-term and accelerated conditions. These results identified that the KPD/HPMC and KPD/PVA-co-PEG solid dispersions were an effective new approach for pharmaceutical application of K. parviflora.

  7. DEVELOPMENT OF CONTINUOUS SOLVENT EXTRACTION PROCESSES FOR COAL DERIVED CARBON PRODUCTS

    Energy Technology Data Exchange (ETDEWEB)

    Elliot B. Kennel; Quentin C. Berg; Stephen P. Carpenter; Dady Dadyburjor; Jason C. Hissam; Manoj Katakdaunde; Liviu Magean; Abha Saddawi; Alfred H. Stiller; John W. Zondlo

    2006-03-07

    The purpose of this DOE-funded effort is to develop continuous processes for solvent extraction of coal for the production of carbon products. The largest applications are those which support metals smelting, such as anodes for aluminum smelting and electrodes for arc furnaces. Other carbon products include materials used in creating fuels for the Direct Carbon Fuel Cell, metals smelting, especially in the aluminum and steel industries, as well as porous carbon structural material referred to as ''carbon foam'' and carbon fibers. During this reporting period, efforts have focused on the development of carbon electrodes for Direct Carbon Fuel Cells (DCFC), and on carbon foam composites used in ballistic armor, as well as the hydrotreatment of solvents used in the basic solvent extraction process. A major goal is the production of 1500 pounds of binder pitch, corresponding to about 3000 pounds of hydrotreated solvent.

  8. Substitution of carcinogenic solvent dichloromethane for the extraction of volatile compounds in a fat-free model food system.

    Science.gov (United States)

    Cayot, Nathalie; Lafarge, Céline; Bou-Maroun, Elias; Cayot, Philippe

    2016-07-22

    Dichloromethane is known as a very efficient solvent, but, as other halogenated solvents, is recognized as a hazardous product (CMR substance). The objective of the present work is to propose substitution solvent for the extraction of volatile compounds. The most important physico-chemical parameters in the choice of an appropriate extraction solvent of volatile compounds are reviewed. Various solvents are selected on this basis and on their hazard characteristics. The selected solvents, safer than dichloromethane, are compared using the extraction efficiency of volatile compounds from a model food product able to interact with volatile compounds. Volatile compounds with different hydrophobicity are used. High extraction yields were positively correlated with high boiling points and high Log Kow values of volatile compounds. Mixtures of solvents such as azeotrope propan-2-one/cyclopentane, azeotrope ethyl acetate/ethanol, and mixture ethyl acetate/ethanol (3:1, v/v) gave higher extraction yields than those obtained with dichloromethane.

  9. Optimization of solvent extraction of shea butter (Vitellaria paradoxa) using response surface methodology and its characterization.

    Science.gov (United States)

    Ajala, E O; Aberuagba, F; Olaniyan, A M; Onifade, K R

    2016-01-01

    Shea butter (SB) was extracted from its kernel by using n-hexane as solvent in an optimization study. This was to determine the optima operating variables that would give optimum yield of SB and to study the effect of solvent on the physico-chemical properties and chemical composition of SB extracted using n-hexane. A Box-behnken response surface methodology (RSM) was used for the optimization study while statistical analysis using ANOVA was used to test the significance of the variables for the process. The variables considered for this study were: sample weight (g), solvent volume (ml) and extraction time (min). The physico-chemical properties of SB extracted were determined using standard methods and Fourier Transform Infrared Spectroscopy (FTIR) for the chemical composition. The results of RSM analysis showed that the three variables investigated have significant effect (p butter extracted using traditional method (SBT) showed that it is a more suitable raw material for food, biodiesel production, cosmetics, medicinal and pharmaceutical purposes than shea butter extracted using solvent extraction method (SBS). Fourier Transform Infrared Spectroscopy (FTIR) results obtained for the two samples were similar to what was obtainable from other vegetable oil.

  10. In vitro antimicrobial potential of organic solvent extracts of novel ...

    African Journals Online (AJOL)

    SAM

    methanol and water extracts of selected promising actinomycetes strains were studied towards Gram- positive ... Streptomyces are used in the production of a diverse array of ..... n-hexane, chloroform, diethyl ether, ethyl acetate, butyl acetate ...

  11. Phytochemical and antioxidant properties of different solvent extracts of Kirkia wilmsii tubers

    Institute of Scientific and Technical Information of China (English)

    Kayini Chigayo; Paul Eanas Lesedi Mojapelo; Simon Mnyakeni-Moleele; Jane Masiiwa Misihairabgwi

    2016-01-01

    Objective: To determine suitable phytochemical extraction solvents, screen for phyto-chemicals, determine the total phenol and flavonoid contents and the antioxidant activities of different solvent extracts of Kirkia wilmsii (K. wilmsii), an ethnomedicine in South Africa. Methods: Extractions were performed from dried tubers of the K. wilmsii plant, using several solvents and varying extraction times. Extract yields were determined and suitable extraction solvents were selected. Total phenol and flavonoid contents of the extracts were determined spectrophotometrically using gallic acid and quercetin as standards. The free radical scav-enging activity of the extracts was investigated using 1,1-diphenyl-2-picrylhydrazyl radical. Results: Phytochemical screening confirmed the presence of phenolics, flavonoids, terpe-noids, tannins, cardenolide deoxy sugars and reducing sugars. Of the 12 solvent extracts used, six gave yields higher than 5%, while the other six gave yields less than 1%. The highest extract yield of 52.9%was obtained using 80%methanol while the lowest yield of 7.3%was obtained using ethanol at 60 min. The 80%methanol, methanol/chloroform/water (12:5:3) and 60%methanol extracts were significantly higher than those of ethanol, methanol and water (P<0.05). Total phenolic content recorded extracts ranged from (45.32 ± 0.50) to (122.84 ± 0.31) mg gallic acid equivalent per gram. A maximum total flavonoid content of (917.02 ± 0.10) mg quercetin equivalent per gram and a minimum of (206.26 ± 0.10) mg quercetin equivalent per gram were recorded for methanol and water, respectively. The flavonoid content for methanol was significantly higher than all the other extracts (P<0.05). The scavenging profiles of K. wilmsii extracts were significantly lower (P<0.05) than that of ascorbic acid and IC50 values ranged from 129.94 mg/mL for methanol to 225.04 mg/mL for water. An IC50 value of 56.52 mg/mL was obtained with ascorbic acid. Conclusions: Ethanol, methanol

  12. ANALYSIS OF BIOACTIVE COMPOUNDS AND ANTIMICROBIAL ACTIVITY OF MARINE ALGAE KAPPAPHYCUS ALVAREZII USING THREE SOLVENT EXTRACTS

    Directory of Open Access Journals (Sweden)

    V. Prabha*, D.J. Prakash and P.N. Sudha

    2013-01-01

    Full Text Available The seaweeds are economically valuable resources, used as food, fodder, fertilizer and medicine and thus useful to mankind in many ways. In the present study, Kappaphycus alvarezii, a marine alga, has been analysed for the presence of bioactive products using three solvent extracts. Antimicrobial activity was also done using the same extracts of seaweed. The results revealed that the selected seaweed has active secondary metabolites and also exhibited antimicrobial activity, mainly in the methanolic extract of Kappaphycus alvarezii.

  13. Pressurized solvent extraction of environmental organic compounds in soils using a supercritical fluid extractor

    Energy Technology Data Exchange (ETDEWEB)

    Li, K.; Landriault, M.; Fingas, M. [Emergencies Science Division, Environmement Canada, Environment Technology Centre, Ontario (Canada); Llompart, M. [Universidad de Santiago de Compostela (Spain). Dept. de Quimica Analitica, Nutricieon y bromatologia, Facultad de Quimica

    1998-11-01

    The applicability of pressurised solvent extraction (PSE) for the quantitative extraction of different of semi-volatiles, including polycyclic aromatic hydrocarbons (PAHs), phenols, polychlorinated biphenyls (PCBs) and total petroleum hydrocarbons have been evaluated. For this study a conventional supercritical fluid extraction (SFE) system, the Suprex SFE/50 was adapted to function as a pressurised solvent extraction system. Solid samples were weighed into the SFE thimble and extracted using conventional extraction solvents instead of superficial carbon dioxide. Parameters such as extraction temperature and effect of modifiers were investigated. Although limited by the 150 deg. C maximum oven temperature, it was found effective extraction could still be carried out in less than 25 min for all the compounds studied. The technique was applied to different real matrices contaminated with hydrocarbons, PAHs and phenols. Validations of the technique were performed using standard reference materials. Recoveries for these matrices were good (> 75 %) and precision was generally less than a 10 % RSD. Extensive comparison of this technique with sonication and with microwave assisted extraction (MAE) were made, and recoveries were found to be comparable to MAE and superior to sonication. (authors) 15 refs.

  14. Research and Application Progress in Countercurrent Solvent Extraction

    Institute of Scientific and Technical Information of China (English)

    贾江涛; 吴声; 廖春生; 严纯华

    2004-01-01

    In this article, the recent progress made by Peking University is briefly introduced. Based on Theory of Countercurrent Extraction established by Prof. Guangxian Xu, the static equilibrium and dynamic process for two- and three-outlet countercurrent extractions, and designed the optimized parameters for the real cascades to separate different rare earth minerals, which can be scaled-up to the industrial process without any further experimental verification were systematically investigated. In order to stabilize the quality of products and improve the capability of automation for extraction process, we have also established an 241Am stimulated X-ray fluorescent energy dispersive method to detect the elemental composition in both organic and aqueous phases, which can be used as an on-line analysis method in practice. Furthermore, the expert system and the control software with open- and close-loop models have been set up. Combined with the detected data from on-line analysis, the flow-rates of extracting, feeding, scrubbing and stripping solutions can be controlled in an optimum status for the industrial cascades. In addition, we have developed a new multi-input and multi-output countercurrent extraction process for separating multi-component rare earth mixture with lower chemical cost and pollution.

  15. Solvent extraction of uranium(Ⅵ)and europium(Ⅲ)from nitrate media by picolinamide

    Institute of Scientific and Technical Information of China (English)

    BAO Bo-Rong; CHENG Qian; CAO Wei-Guo; XIANG Qun; LI Yu; ZHAO Yu-Jia

    2005-01-01

    The solvent extraction of uranium(Ⅵ) and europium(Ⅲ) from nitric acid solution was studied with picolinamide dissolved in ethylene dichloride. The distribution ratios of U(Ⅵ) and Eu(Ⅲ) as a function of aqueous HNO3 concentration, extractant concentration in organic phase and temperature as well as the salting-out agent concentration have been measured. The experiment results show that picolinamide has higher extractability for U(Ⅵ1)than for Eu(Ⅲ). The composition of extracted species, equilibrium constants and enthalpies of extraction reaction have also been presented.

  16. Predictive model for ionic liquid extraction solvents for rare earth elements

    Science.gov (United States)

    Grabda, Mariusz; Oleszek, Sylwia; Panigrahi, Mrutyunjay; Kozak, Dmytro; Eckert, Franck; Shibata, Etsuro; Nakamura, Takashi

    2015-12-01

    The purpose of our study was to select the most effective ionic liquid extraction solvents for dysprosium (III) fluoride using a theoretical approach. Conductor-like Screening Model for Real Solvents (COSMO-RS), based on quantum chemistry and the statistical thermodynamics of predefined DyF3-ionic liquid systems, was applied to reach the target. Chemical potentials of the salt were predicted in 4,400 different ionic liquids. On the base of these predictions set of ionic liquids' ions, manifesting significant decrease of the chemical potentials, were selected. Considering the calculated physicochemical properties (hydrophobicity, viscosity) of the ionic liquids containing these specific ions, the most effective extraction solvents for liquid-liquid extraction of DyF3 were proposed. The obtained results indicate that the COSMO-RS approach can be applied to quickly screen the affinity of any rare earth element for a large number of ionic liquid systems, before extensive experimental tests.

  17. Predictive model for ionic liquid extraction solvents for rare earth elements

    Energy Technology Data Exchange (ETDEWEB)

    Grabda, Mariusz; Oleszek, Sylwia [Institute of Multidisciplinary Research for Advanced Materials (IMRAM), Tohoku University, 2,1-Katahira, 2-Chome, 980-8577 Sendai (Japan); Institute of Environmental Engineering of the Polish Academy of Sciences, ul. M. Sklodowskiej-Curie 34, 41-819, Zabrze (Poland); Panigrahi, Mrutyunjay; Kozak, Dmytro; Shibata, Etsuro; Nakamura, Takashi [Institute of Multidisciplinary Research for Advanced Materials (IMRAM), Tohoku University, 2,1-Katahira, 2-Chome, 980-8577 Sendai (Japan); Eckert, Franck [COSMOlogic GmbH & Co KG, Imbacher Weg 46, 50379 Leverkusen (Germany)

    2015-12-31

    The purpose of our study was to select the most effective ionic liquid extraction solvents for dysprosium (III) fluoride using a theoretical approach. Conductor-like Screening Model for Real Solvents (COSMO-RS), based on quantum chemistry and the statistical thermodynamics of predefined DyF{sub 3}-ionic liquid systems, was applied to reach the target. Chemical potentials of the salt were predicted in 4,400 different ionic liquids. On the base of these predictions set of ionic liquids’ ions, manifesting significant decrease of the chemical potentials, were selected. Considering the calculated physicochemical properties (hydrophobicity, viscosity) of the ionic liquids containing these specific ions, the most effective extraction solvents for liquid-liquid extraction of DyF{sub 3} were proposed. The obtained results indicate that the COSMO-RS approach can be applied to quickly screen the affinity of any rare earth element for a large number of ionic liquid systems, before extensive experimental tests.

  18. Thermal Properties of Simulated and High-Level Waste Solutions Used for the Solvent Extraction Demonstration

    Energy Technology Data Exchange (ETDEWEB)

    Fondeur, F.F.

    2001-06-27

    Researchers measured the heat capacity and thermal conductivity of supernate from a blend of Tank 37H and 44F, of a simulant of this blend, and of a simulant specifically designed for solvent extraction experiments. The measured heat capacity of the blend from the Tanks 37H and 44F equaled 0.871 cal/(g degrees C). The simulant of this blend produced an identical result. The heat capacity of the simulant designed for solvent extraction testing equaled 0.859 cal/(g degrees C). All three solutions have thermal conductivities in the range of 0.54 to 0.6 Watts/(m degrees C). The slight variation in the thermophysical properties of these solutions successfully explains the different flowmeter readings observed during the real waste demonstration of the solvent extraction technology.

  19. PURIFICATION OF COBALT ANOLYTE USING THE NOVEL SOLVENT EXTRACTION SYSTEM

    Institute of Scientific and Technical Information of China (English)

    Y.F. Shen; W.Y. Xue; W. Y. Niu

    2003-01-01

    In present research, a novel extractant system (D2EHPA + naphthenic acid +pyridine-ester) was used to purify cobalt anolyte and a simulated industrial produc-tion were carried out. This novel extraction system can extract Cu and/or Ni againstCo from chloride medium solutions at pH range of 2.5-4.5. About 2g/l nickel and0.2g/l copper were removed from the cobalt chloride anolyte containing about 100g/lcobalt and 200g/l chloride ions respectively, the raffinate contains nickel and copperless than 0.03g/l and 0. 0003g/l respectively and can be used to electrolyze high-puritycobalt. About 5.5t cobalt anolyte was purified in the simulation industrial experimentand kilogram quantities of cobalt of 99.98% purity and about 95% recovery have beenproduced.

  20. Efficient solvent extraction of antioxidant-rich extract from a tropical diatom,Chaetoceros calcitrans (Paulsen) Takano 1968

    Institute of Scientific and Technical Information of China (English)

    Su Chern Foo; Fatimah Md Yusoff; Maznah Ismail; Mahiran Basri; Nicholas Mun Hoe Khong; Kim Wei Chan; Sook Kun Yau

    2015-01-01

    Objective:To compare thein vitro antioxidant capacity of a diatom,Chaetoceros calcitrans (C. calcitrans) extracted using six types of solvents. Methods:Each extract was evaluated in terms of extraction yield, total carotenoid, fucoxanthin content, total phenolic and antioxidant capacities (DPPH• andABTS•+ scavenging activity and iron chelating activity). Results: The methanol extract exhibited the highest yield [(22.71 ± 0.96) g/100 g dry weight (DW)], total carotenoid [(4.46 ± 0.36) mg/g DW], total phenolic [(2.49 ± 0.08) mg gallic acid equivalents/g DW] and second highest fucoxanthin content [(2.08 ± 0.03) mg fucoxanthin/g DW] as compared to other solvent extracts. Methanolic extract also exhibited significantly higher (P Conclusions: Methanol was the recommended solvent for the production of antioxidant rich extract fromC. calcitrans. Both carotenoids and phenolic acids were found to be positively correlated to the antioxidant capacities ofC. calcitrans. Lead bioactives confirmed by subsequent high performance liquid chromatography studies were fucoxanthin, gallic acid and protocatechuic acid.

  1. Efficient solvent extraction of antioxidant-rich extract from a tropical diatom,Chaetoceros calcitrans (Paulsen) Takano 1968简

    Institute of Scientific and Technical Information of China (English)

    Su; Chern; Foo; Fatimah; Md.Yusoff; Maznah; Ismail; Mahiran; Basri; Nicholas; Mun; Hoe; Khong; Kim; Wei; Chan; Sook; Kun; Yau

    2015-01-01

    Objective: To compare the in vitro antioxidant capacity of a diatom, Chaetoceros calcitrans(C. calcitrans) extracted using six types of solvents.Methods: Each extract was evaluated in terms of extraction yield, total carotenoid,fucoxanthin content, total phenolic and antioxidant capacities(DPPH and ABTS +scavenging activity and iron chelating activity).Results: The methanol extract exhibited the highest yield [(22.71 ± 0.96) g/100 g dry weight(DW)], total carotenoid [(4.46 ± 0.36) mg/g DW], total phenolic [(2.49 ± 0.08) mg gallic acid equivalents/g DW] and second highest fucoxanthin content [(2.08 ± 0.03) mg fucoxanthin/g DW] as compared to other solvent extracts. Methanolic extract also exhibited significantly higher(P < 0.05) scavenging(DPPH, ABTS +) and iron chelating activities.Conclusions: Methanol was the recommended solvent for the production of antioxidant rich extract from C. calcitrans. Both carotenoids and phenolic acids were found to be positively correlated to the antioxidant capacities of C. calcitrans. Lead bioactives confirmed by subsequent high performance liquid chromatography studies were fucoxanthin, gallic acid and protocatechuic acid.

  2. Water as a green solvent combined with different techniques for extraction of essential oil from lavender flowers

    OpenAIRE

    2016-01-01

    Using water as a green solvent with a variable geometry makes use of physical and chemical phenomena that are fundamentally different from those applied in conventional extraction techniques such as hydro-distillation, steam distillation or solvent extraction. Advantages and drawbacks of using water as a solvent with different physical and chemical states have been compared. A total of ten extraction techniques: hydro-distillation (HD), steam distillation (SD), turbo-hydro-distillation (THD),...

  3. Use of solvent mixtures for total lipid extraction of Chlorella vulgaris and gas chromatography FAME analysis.

    Science.gov (United States)

    Moradi-Kheibari, Narges; Ahmadzadeh, Hossein; Hosseini, Majid

    2017-06-07

    Lipid extraction is the bottleneck step for algae-based biodiesel production. Herein, 12 solvent mixture systems (mixtures of three non-polar and two polar organic solvents) were examined to evaluate their effects on the total lipid yield from Chlorella vulgaris (C. vulgaris). Moreover, the extraction yields of three solvent systems with maximum extraction efficiency of esterifiable lipids were determined by acidic transesterification and GC-FID analysis. Three solvent systems, which resulted in a higher extraction yield, were further subjected to fatty acid methyl ester (FAME) analysis. The total lipid extraction yields (based on dry biomass) were (38.57 ± 1.51), (25.33 ± 0.58), and (25.17 ± 1.14) %, for chloroform-methanol (1:2) (C1M2), hexane-methanol (1:2) (H1M2), and chloroform-methanol (2:1) (C2M1), respectively. The extraction efficiency of C1M2 was approximately 1.5 times higher than H1M2 and C2M1, whereas the FAME profile of extracted lipids by H1M2 and C1M2 were almost identical. Moreover, the esterifiable lipid extraction yields of (18.14 ± 2.60), (16.66 ± 0.35), and (13.22 ± 0.31) % (based on dry biomass) were obtained for C1M2, H1M2, and C2M1 solvent mixture systems, respectively. The biodiesel fuel properties produced from C. vulgaris were empirically predicted and compared to that of the EN 14214 and ASTM 6751 standard specifications.

  4. Extractant selection strategy for solvent-impregnated resins in fermentations

    NARCIS (Netherlands)

    Berg, C. van den; Roelands, C.P.M.; Bussmann, P.J.Th.; Goetheer, E.L.V.; Verdoes, D.; Wielen, L. van der

    2008-01-01

    The application of extractants in whole-cell biocatalysis can have a positive impact on industrial fermentations, in terms of productivity, total amount of product produced, and cell growth. When a product is continuously removed from the microorganism surroundings, product inhibition will be dimini

  5. Isotope effects of hafnium in solvent extraction using crown ethers

    Energy Technology Data Exchange (ETDEWEB)

    Fujii, Toshiyuki; Moriyama, Hirotake [Research Reactor Institute, Kyoto University, Osaka (Japan); Hirata, Takafumi [Laboratory for Planetary Sciences, Tokyo Institute of Technology, Tokyo (Japan); Nishizawa, Kazushige [Department of Nuclear Engineering, Graduate School of Engineering, Osaka University, Osaka (Japan)

    2001-06-01

    Hafnium isotopes were fractionated in a liquid-liquid extraction system by using seven types of crown ethers, tributyl phosphate, or {omicron}-diethoxybenzene. The largest isotope effect was observed in the isotope pair of {sup 177}Hf-{sup 179}Hf with dibenzo-24-crown-8; the isotope enrichment factor was observed to be 0.0129{+-}0.0032. (author)

  6. Ultrasound-assisted extraction (UAE) and solvent extraction of papaya seed oil: yield, fatty acid composition and triacylglycerol profile.

    Science.gov (United States)

    Samaram, Shadi; Mirhosseini, Hamed; Tan, Chin Ping; Ghazali, Hasanah Mohd

    2013-10-10

    The main objective of the current work was to evaluate the suitability of ultrasound-assisted extraction (UAE) for the recovery of oil from papaya seed as compared to conventional extraction techniques (i.e., Soxhlet extraction (SXE) and solvent extraction (SE)). In the present study, the recovery yield, fatty acid composition and triacylglycerol profile of papaya seed oil obtained from different extraction methods and conditions were compared. Results indicated that both solvent extraction (SE, 12 h/25 °C) and ultrasound-assisted extraction (UAE) methods recovered relatively high yields (79.1% and 76.1% of total oil content, respectively). Analysis of fatty acid composition revealed that the predominant fatty acids in papaya seed oil were oleic (18:1, 70.5%-74.7%), palmitic (16:0, 14.9%-17.9%), stearic (18:0, 4.50%-5.25%), and linoleic acid (18:2, 3.63%-4.6%). Moreover, the most abundant triacylglycerols of papaya seed oil were triolein (OOO), palmitoyl diolein (POO) and stearoyl oleoyl linolein (SOL). In this study, ultrasound-assisted extraction (UAE) significantly (p < 0.05) influenced the triacylglycerol profile of papaya seed oil, but no significant differences were observed in the fatty acid composition of papaya seed oil extracted by different extraction methods (SXE, SE and UAE) and conditions.

  7. Ultrasound-Assisted Extraction (UAE and Solvent Extraction of Papaya Seed Oil: Yield, Fatty Acid Composition and Triacylglycerol Profile

    Directory of Open Access Journals (Sweden)

    Hasanah Mohd Ghazali

    2013-10-01

    Full Text Available The main objective of the current work was to evaluate the suitability of ultrasound-assisted extraction (UAE for the recovery of oil from papaya seed as compared to conventional extraction techniques (i.e., Soxhlet extraction (SXE and solvent extraction (SE. In the present study, the recovery yield, fatty acid composition and triacylglycerol profile of papaya seed oil obtained from different extraction methods and conditions were compared. Results indicated that both solvent extraction (SE, 12 h/25 °C and ultrasound-assisted extraction (UAE methods recovered relatively high yields (79.1% and 76.1% of total oil content, respectively. Analysis of fatty acid composition revealed that the predominant fatty acids in papaya seed oil were oleic (18:1, 70.5%–74.7%, palmitic (16:0, 14.9%–17.9%, stearic (18:0, 4.50%–5.25%, and linoleic acid (18:2, 3.63%–4.6%. Moreover, the most abundant triacylglycerols of papaya seed oil were triolein (OOO, palmitoyl diolein (POO and stearoyl oleoyl linolein (SOL. In this study, ultrasound-assisted extraction (UAE significantly (p < 0.05 influenced the triacylglycerol profile of papaya seed oil, but no significant differences were observed in the fatty acid composition of papaya seed oil extracted by different extraction methods (SXE, SE and UAE and conditions.

  8. Mechanism of gold solvent extraction from aurocyanide solution by quaternary amines: models of extracting species based on hydrogen bonding

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The mechanism of gold solvent extraction from KAu(CN)2 solution was investigated by means of FTIR, EXAFS, ICP and radioactive tracer methods. Two extraction systems were studied, namely N263-tributyl phosphate(TBP)-n-dodecane and N263-iso-octanol-n-dodecane. High-reso- lution FT IR spectroscopy indicated that the CN stretching vibrations of the two extraction systems differred greatly. In order to interpret the significant difference in CN stretching vibrations, two extracting species models are proposed supramolecular structures based on the formation of hydrogen bonds between Au(CN)2- and modifiers such as TBP and iso-octanol.

  9. Evaluation of the antioxidant and antibacterial properties of various solvents extracts of Annona squamosa L. leaves

    Directory of Open Access Journals (Sweden)

    Ghadir A. El-Chaghaby

    2014-04-01

    Full Text Available The present work was conducted aiming to evaluate the effect of different solvent extracts on the antioxidant and antibacterial activities of Annona squamosa L. leaves. Four solvents were chosen for the study namely; methanol 80%, acetone 50%, ethanol 50% and boiling water. Acetone and boiling water gave the highest extraction yields as compared to methanol and ethanol. Total phenolic contents of the four extracts were significantly different with acetone being the most efficient solvent and water being the least efficient one. Correlation coefficient between the total antioxidant and total phenolic content was found to be R2 = 0.89 suggesting the contribution of phenolic compounds of the extract by 89% to its total antioxidant activity. The extracts were capable of scavenging H2O2 in a range of 43–54%. Reducing power of the extracts increased by increasing their concentration. The extracts were found to exert low to moderate antibacterial activity compared to a standard antibacterial agent. The bacterial inhibition of the extracts was found to positively correlate with their phenolic contents.

  10. Determination of Technetium-99 in Environmental Samples by Solvent Extraction at Controlled Valence

    DEFF Research Database (Denmark)

    Chen, Q.J.; Aarkrog, A.; Dahlgaard, H.

    1989-01-01

    Distribution coefficients of technetium and ruthenium are determined under different conditions with CCl4, cyclohexanone, and 5% tri-isooctylamine (TIOA)/xylene. A method for analyzing 99Tc in environmental samples has been developed by solvent extraction in which the valences of technetium...... are subsequently separated by solvent extraction with cyclohexanone and 5% TIOA/xylene. The decontamination of the procedure is 1.35 .cntdot. 105 for 103Ru and 1.66 .cntdot. 105 for 110mAg. The chemical yield of technetium-99 is 55%....

  11. Stable Isotope-Assisted Evaluation of Different Extraction Solvents for Untargeted Metabolomics of Plants

    Directory of Open Access Journals (Sweden)

    Maria Doppler

    2016-06-01

    Full Text Available The evaluation of extraction protocols for untargeted metabolomics approaches is still difficult. We have applied a novel stable isotope-assisted workflow for untargeted LC-HRMS-based plant metabolomics , which allows for the first time every detected feature to be considered for method evaluation. The efficiency and complementarity of commonly used extraction solvents, namely 1 + 3 (v/v mixtures of water and selected organic solvents (methanol, acetonitrile or methanol/acetonitrile 1 + 1 (v/v, with and without the addition of 0.1% (v/v formic acid were compared. Four different wheat organs were sampled, extracted and analysed by LC-HRMS. Data evaluation was performed with the in-house-developed MetExtract II software and R. With all tested solvents a total of 871 metabolites were extracted in ear, 785 in stem, 733 in leaf and 517 in root samples, respectively. Between 48% (stem and 57% (ear of the metabolites detected in a particular organ were found with all extraction mixtures, and 127 of 996 metabolites were consistently shared between all extraction agent/organ combinations. In aqueous methanol, acidification with formic acid led to pronounced pH dependency regarding the precision of metabolite abundance and the number of detectable metabolites, whereas extracts of acetonitrile-containing mixtures were less affected. Moreover, methanol and acetonitrile have been found to be complementary with respect to extraction efficiency. Interestingly, the beneficial properties of both solvents can be combined by the use of a water-methanol-acetonitrile mixture for global metabolite extraction instead of aqueous methanol or aqueous acetonitrile alone.

  12. 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.

  13. Selective Extraction of Bio-oil from Hydrothermal Liquefaction of Salix psammophila by Organic Solvents with Different Polarities through Multistep Extraction Separation

    OpenAIRE

    Xiao Yang; Hang Lyu; Kaifei Chen; Xiangdong Zhu; Shicheng Zhang; Jianmin Chen

    2014-01-01

    Bio-oil obtained from hydrothermal liquefaction of Salix psammophila is a very complicated mixture with some highly valued chemicals. In order to separate the chemicals from bio-oil, solvent extraction using nine solvents with different polarities were investigated in detail. The bio-oil extraction yield of the nine solvents were from high to low: tetrahydrofuran > toluene > ethyl acetate > acetone > ether > methylene chloride > methanol > petroleum ether > n-hexane. Based on their extraction...

  14. Efficient solvent extraction of antioxidant-rich extract from a tropical diatom, Chaetoceros calcitrans (Paulsen Takano 1968

    Directory of Open Access Journals (Sweden)

    Su Chern Foo

    2015-10-01

    Conclusions: Methanol was the recommended solvent for the production of antioxidant rich extract from C. calcitrans. Both carotenoids and phenolic acids were found to be positively correlated to the antioxidant capacities of C. calcitrans. Lead bioactives confirmed by subsequent high performance liquid chromatography studies were fucoxanthin, gallic acid and protocatechuic acid.

  15. CHEMICAL FIXATION OF CARBON DIOXIDE USING SOLVENT EXTRACTION

    OpenAIRE

    SASAMOTO, Naoki; MASHIMO, Miki; MATSUMOTO, Shigeno; Yamamoto, Hideki; SHIBATA, Junji

    1996-01-01

    Investigations were carried out to create a chemical fixation process,where carbon dioxide and sodium chloride solution are converted to sodium hydrogen carbonate and hydrochloric acid. Because the reaction has a large and positive free energy change,it does not proceed unless a suitable condition is established.The reaction is able to proceed if hydrochloric acid,which is one of the reaction products,is removed from the reaction system by extraction with amine.Stripping of hydrochloric acid ...

  16. Kinetics and Thermodynamics of Oil Extraction from Jatropha curcas L. Using Ethanol as a Solvent

    Directory of Open Access Journals (Sweden)

    Silmara Bispo dos Santos

    2015-01-01

    Full Text Available In the study the yield and kinetic and thermodynamic parameters of the oil extraction process from Jatropha curcas L. using ethanol as a solvent were evaluated for different temperatures, moisture contents of the solid phase, and particle sizes. The extraction process yield increased with contact time of solid particles with the solvent until reaching equilibrium (saturation of the solvent, for all the temperatures, moisture contents, and average particle sizes. These parameters significantly influenced (95% confidence the extracted oil yield. A convective mass transfer model was used to simulate the extraction process and estimate the kinetic and thermodynamic parameters. For all conditions evaluated, values of oil yield in the liquid phase close to equilibrium were obtained in approximately 20 min. The variations of enthalpy and entropy were positive, indicating that the process is endothermic and irreversible. Values obtained for the variation in Gibbs free energy showed that the extraction process using ethanol as a solvent is spontaneous and thermodynamically favorable for the moisture content of 0%, where the smaller the average particle size the greater the spontaneity of the process.

  17. Extraction of basil leaves (ocimum canum) oleoresin with ethyl acetate solvent by using soxhletation method

    Science.gov (United States)

    Tambun, R.; Purba, R. R. H.; Ginting, H. K.

    2017-09-01

    The goal of this research is to produce oleoresin from basil leaves (Ocimum canum) by using soxhletation method and ethyl acetate as solvent. Basil commonly used in culinary as fresh vegetables. Basil contains essential oils and oleoresin that are used as flavouring agent in food, in cosmetic and ingredient in traditional medicine. The extraction method commonly used to obtain oleoresin is maceration. The problem of this method is many solvents necessary and need time to extract the raw material. To resolve the problem and to produce more oleoresin, we use soxhletation method with a combination of extraction time and ratio from the material with a solvent. The analysis consists of yield, density, refractive index, and essential oil content. The best treatment of basil leaves oleoresin extraction is at ratio of material and solvent 1:6 (w / v) for 6 hours extraction time. In this condition, the yield of basil oleoresin is 20.152%, 0.9688 g/cm3 of density, 1.502 of refractive index, 15.77% of essential oil content, and the colour of oleoresin product is dark-green.

  18. Review on aggregation of acid extractants in solvent extraction of metal ions: remark on the general model

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    The aggregation behavior of various acid extractants in the solvent extraction systems of metal ions is re-examined and explained according to knowledge obtained in recent work. The conclusions are as follows. (1) Complexes formed by the extractants and metal ions can form reversed micelles in organic diluents, depending on the microstructures of the complexes. The dimers of the acid extractant cannot percolate to the metal-extractant aggregates, and the acid-salt complexes are always formed in the aggregates. The reversed micelles or the W/O microemulsions formed by different species cannot be associated with each other to form a unified aggregate. (2) In solvent extraction systems, hydration of the extractants and metal ions can be considered as the driving force of forming reversed micelles. (3) Information of the first approach to the insight of the bicontinuous microemulsion of NaDEHP shows that various components in the aqueous phase behave confined and very similar to the typical AOT/n-heptane W/O microemulsions. (4) In the extraction of lanthanide ions by the W/O microemulsion of sodium naphthenate, the saponification is a process of forming reversed micelle or W/O microemulsion, while the extraction step is a process of destroying reversed micelles or W/O microemulsion droplets.

  19. Cogeneration of biodiesel and nontoxic cottonseed meal from cottonseed processed by two-phase solvent extraction

    Energy Technology Data Exchange (ETDEWEB)

    Qian, Junfeng [Jiangsu Provincial Key Laboratory of Fine Petrochemical Engineering, Jiangsu Polytechnic University, Changzhou 213016 (China); College of Chemistry and Chemical Engineering, Nanjing University of Technology, Nanjing 210009 (China); Yun, Zhi; Shi, Haixian [College of Chemistry and Chemical Engineering, Nanjing University of Technology, Nanjing 210009 (China)

    2010-12-15

    In the present work, the preparation of biodiesel from cottonseed oil produced by two-phase solvent extraction (TSE) was studied. The experimental results of TSE process of cottonseed showed that the optimal extraction conditions were 30 g samples, 240 mL extraction solvent mixture and methanol/petroleum ether volume ratio 60:40, extraction temperature 30 C, extraction time 30 min. Under the extraction conditions, the extraction rate of cottonseed oil could achieve 98.3%, the free fatty acid (FFA) and water contents of cottonseed oil were reduced to 0.20% and 0.037%, respectively, which met the requirement of alkali-catalyzed transesterification. The free gossypol (FG) content in cottonseed meal produced from two-phase solvent extraction could reduce to 0.014% which was far below the FAO standard. And the nontoxic cottonseed meal could be used as animal protein feed resources. After the TSE process of cottonseed, the investigations were carried out on transesterification of methanol with oil-petroleum ether solution coming from TSE process in the presence of sodium hydroxide (CaO) as the solid base catalyst. The influences of weight ratio of petroleum ether to cottonseed oil, reaction temperature, molar ratio of methanol to oil, alkali catalyst amount and reaction time on cottonseed oil conversion were respectively investigated by mono-factor experiments. The conversion of cottonseed oil into fatty acid methyl ester (FAME) could achieve 98.6% with 3:1 petroleum ether/oil weight ratio, 65 C reaction temperature, 9:1 methanol/oil mole ratio, 4% (catalyst/oil weight ratio, w/w) solid base catalyst amount and 3 h reaction time. The properties of FAME product prepared from cottonseed oil produced by two-phase solvent extraction met the ASTM specifications for biodiesel. (author)

  20. Cogeneration of biodiesel and nontoxic cottonseed meal from cottonseed processed by two-phase solvent extraction

    Energy Technology Data Exchange (ETDEWEB)

    Qian Junfeng, E-mail: qianjunfeng80@126.co [Jiangsu Provincial Key Laboratory of Fine Petrochemical Engineering, Jiangsu Polytechnic University, Changzhou 213016 (China) and College of Chemistry and Chemical Engineering, Nanjing University of Technology, Nanjing 210009 (China); Yun Zhi; Shi Haixian [College of Chemistry and Chemical Engineering, Nanjing University of Technology, Nanjing 210009 (China)

    2010-12-15

    In the present work, the preparation of biodiesel from cottonseed oil produced by two-phase solvent extraction (TSE) was studied. The experimental results of TSE process of cottonseed showed that the optimal extraction conditions were 30 g samples, 240 mL extraction solvent mixture and methanol/petroleum ether volume ratio 60:40, extraction temperature 30 deg. C, extraction time 30 min. Under the extraction conditions, the extraction rate of cottonseed oil could achieve 98.3%, the free fatty acid (FFA) and water contents of cottonseed oil were reduced to 0.20% and 0.037%, respectively, which met the requirement of alkali-catalyzed transesterification. The free gossypol (FG) content in cottonseed meal produced from two-phase solvent extraction could reduce to 0.014% which was far below the FAO standard. And the nontoxic cottonseed meal could be used as animal protein feed resources. After the TSE process of cottonseed, the investigations were carried out on transesterification of methanol with oil-petroleum ether solution coming from TSE process in the presence of sodium hydroxide (CaO) as the solid base catalyst. The influences of weight ratio of petroleum ether to cottonseed oil, reaction temperature, molar ratio of methanol to oil, alkali catalyst amount and reaction time on cottonseed oil conversion were respectively investigated by mono-factor experiments. The conversion of cottonseed oil into fatty acid methyl ester (FAME) could achieve 98.6% with 3:1 petroleum ether/oil weight ratio, 65 deg. C reaction temperature, 9:1 methanol/oil mole ratio, 4% (catalyst/oil weight ratio, w/w) solid base catalyst amount and 3 h reaction time. The properties of FAME product prepared from cottonseed oil produced by two-phase solvent extraction met the ASTM specifications for biodiesel.

  1. Solvent extraction of cadmium and zinc from sulphate solutions: Comparison of mechanical agitation and ultrasonic irradiation.

    Science.gov (United States)

    Daryabor, Mahboubeh; Ahmadi, Ali; Zilouei, Hamid

    2017-01-01

    This research was conducted to evaluate the potential of ultrasonic irradiation during the solvent extraction of metals, and comparing its efficiency with a mechanically stirred system (MSSX). The simultaneous extraction of zinc and cadmium from sulphate solutions was investigated by di-(2-ethylhexyl) phosphoric acid (D2EHPA) as an organic extractant which was diluted (20%) in kerosene at the organic: aqueous phase ratio of 1:1 and the temperature of 25°C. The influence of some critical parameters, including contact time, solution pH, ultrasonic power, and zinc/cadmium ratio were investigated on the extraction of the metals. Results show that D2EHPA selectively extract zinc rather than cadmium in both mechanically and ultrasonically mixed systems. It was also found that increase of ultrasonic power from 10 to 120W cause a small decrease in zinc extraction; while, at low and high levels of the induced power, cadmium extraction was significantly decreased. Results also show that maximum extraction amounts of zinc (88.7%) and cadmium (68.2%) by the MSSX system occurred at the pH of 3 and the contact times of 3 and 20min, respectively. Although capability of extraction in the ultrasonically assisted solvent extraction (USAX) system for both metals was higher, the selectivity was lower than that of MSSX system under different conditions especially in high zinc/cadmium ratios. It can be concluded that physical effects (i.e. mixing) inducing at low ultrasonic powers (below 60W) mainly results in increasing solvent extraction rate, while the chemical actions applied at the higher powers have a negative outcome on the extraction rate particularly for cadmium.

  2. Extraction of thymol from different varieties of thyme plants using green solvents.

    Science.gov (United States)

    Villanueva Bermejo, David; Angelov, Ivan; Vicente, Gonzalo; Stateva, Roumiana P; Rodriguez García-Risco, Mónica; Reglero, Guillermo; Ibañez, Elena; Fornari, Tiziana

    2015-11-01

    Thymol (2-isopropyl-5-methylphenol) is the main monoterpene phenol found in thyme essential oil. This compound has revealed several biological properties, including antibacterial, anti-inflammatory and antioxidant activities. In this work, a comparison was made between the performance of different green solvents (ethanol, limonene and ethyl lactate), by pressurized liquid extraction (PLE) and supercritical fluid extraction (SFE) at different conditions, to extract thymol from three different varieties of thyme (Thymus vulgaris, Thymus zygis and Thymus citriodorus). Additionally, new solubility data of thymol in limonene and ethanol at ambient pressure and temperatures in the range 30-43 °C are reported. The highest thymol recoveries were attained with T. vulgaris (7-11 mg g(-1)). No thymol could be quantified in the PLE samples of T. citriodorus. The highest concentrations of thymol in the extracts were obtained with limonene. Thymol is very soluble in both solvents, particularly in ethanol (∼900 mg g(-1) at ∼40 °C), and is the main compound (in terms of peak area) present in the essential oil extracts obtained. The three solvents show good capacity to extract thymol from T. vulgaris and T. zygis by PLE. Although PLE proved to be a suitable technology to extract thymol from thyme plants, the highest concentrations of thymol were obtained by SFE with supercritical CO2 . © 2014 Society of Chemical Industry.

  3. Effect of different format-solvent rosemary extracts (Rosmarinus officinalis) on frozen chicken nuggets quality.

    Science.gov (United States)

    Rocío Teruel, M; Garrido, M Dolores; Espinosa, Miriam C; Linares, M Belén

    2015-04-01

    Three kinds of Rosmarinus officinalis extract (powder-acetone, liquid-methanol, liquid-acetone) were used to examine the effects of format-solvent on the active compounds extracted (total phenolic, carnosol and carnosic acid content) and antioxidant activity (FRAP, ABTS). The results showed that both, as the format but also the solvent used, had significant effect on the parameters analyzed (p < 0.05). The highest antioxidant activity was found for the powder-acetone extract followed by the liquid methanol and liquid acetone extracts (p < 0.05). The effect of the three different extracts on the physical-chemical and sensory quality of frozen chicken nuggets was evaluated. At the dose proposed by the European Union Directive 2010/69/EU for the carnosic and carnosol compounds [150 ppm (mg/kg fat basic)], the format-solvent combination of the rosemary extracts used did not modify the chicken nuggets quality characteristics (pH, colour, sensory quality) and still underlines the effectiveness of these extracts.

  4. Radiation influencing of the extraction properties of the CyMe{sub 4}-BTBP and CyMe{sub 4}-BTPhen solvents with FS-13

    Energy Technology Data Exchange (ETDEWEB)

    Konde, J.; Distler, P.; John, J. [Department of Nuclear Chemistry, Czech Technical University in Prague, BGehova 7, 11519 Prague 1 (Czech Republic); Svehla, J.; Gruner, B.; Belcicka, Z. [Institute of Inorganic Chemistry, Academy of Sciences of the Czech Republic, 250 68 Rez near Prague (Czech Republic)

    2016-07-01

    The radiolytic stability of two ligands, CyMe4-BTBP and CyMe4-BTPhen in system with the FS-13 (phenyl trifluoromethyl sulfone) diluent was investigated under irradiation by accelerated electrons to study impact of the degradation products on the separation process efficiency and safety. Irradiation experiments were carried out up to the absorbed dose of 200 kGy. The irradiated samples were analysed by HPLC for the degree of extractant degradation. In addition, the effect of the presence of HNO{sub 3} during the irradiation was studied. Extraction properties of the irradiated solvents were evaluated and compared with the extraction properties of non-irradiated solvents to assess the impact of the degradation products on extractions properties. The results obtained show that the stabilities of these ligands are higher in FS-13 than in the cyclohexanone-type solvents. The extraction properties are significantly influenced by degradation products contained in these systems. Surprisingly, both the distribution ratios for americium and europium, and the Am/Eu separation factor increase with the absorbed dose for the system withCyMe{sub 4}-BTPhen in FS-13. Obviously, the degradation products of this ligand are efficient extractants too. In the next phase, an attempt will be done to identify the main degradation products, synthesise them and study their extraction properties. (authors)

  5. Studies on antimicrobial activities of solvent extracts of different spices.

    Science.gov (United States)

    Keskin, Dilek; Toroglu, Sevil

    2011-03-01

    The antimicrobial activities of the ethyl acetate, acetone and methanol extract of 12 plant species were studied. The extract of Capsicum annuum (red pepper) (fruit) Zingiber officinale (ginger) (root), Cuminum cyminum (cumin), Alpinia ficinarum (galingale), Coriandrum sativum (coriander), Cinnamomun zeylanicum Nees (cinnamomun), Origanum onites L. (thyme), Folium sennae (senna), Eugenia caryophyllata (cloves), Flos tiliae (lime), Folium menthae crispae (peppermint) and Piper nigrum (blackpepper) were tested in vitro against 2 fungi and 8 bacterial species by the disc diffusion method. Klebsiella pneumonia 13883, Bacillus megaterium NRS, Pseudomonas aeroginosa ATCC 27859, Staphylococcus aureus 6538 P, Escherichia coil ATCC 8739, Enterobacter cloaca ATCC 13047, Corynebacterium xerosis UC 9165, Streptococcus faecalis DC 74, Kluyveromyces marxianus, Rhodotorula rubra were used in this investigation. The results indicated that extracts of different spices has shown antibacterial activity in the range of 7-24 mm 30 microl(-1) inhibition zone Eugenia caryophyllata (clove), 7-20 mm 30microl(-1) inhibition zone Capsicum annum (red pepper) and Cinnamomun zeylanicum (cinnamon) bark, 7-18 mm 30microl(-1) inhibition zone Folium sennae (senna) leaves, 7-16 mm 30 microl(-1) inhibition zone Zingiber officinale (ginger) root, 7-15 mm 30microl(-1) inhibition zone Cuminum cyminum (cumin) seed, 7-14 mm 30 microl(-1) inhibition zone Folium menthae crispae (peppermint), Origanum onites (thyme) leaves and Alpinia ficinarum (galingale) root, 7-12 mm 30 microl(-1) inhibiton zone Piper nigrum (blackpepper), 7-11 mm 30microl(-1) inhibition zone Flos tiliae (lime) leaves, 7-8 mm 30microl(-1) inhibition zone Coriandrum sativum (coriander) to the microorganisms tested.

  6. Solvent extraction equipment evaluation study. Part 3. Summary

    Energy Technology Data Exchange (ETDEWEB)

    Browne, L.M.; Geier, R.G.

    1977-01-01

    This document reviews the available literature on the types of liquid-liquid extraction contactors used to perform radiochemical separations. Also included are comparisons between the types of contactors. The summarization of each of the approximately 130 papers reviewed contains a description of the equipment tested, the chemical system used to test it, and the results obtained. Conclusions drawn by the original authors have not been altered. A bibliography has been included which has been numbered to cross-reference the summaries to the proper references.

  7. Solvent extraction in the treatment of acidic high-level liquid waste : where do we stand?

    Energy Technology Data Exchange (ETDEWEB)

    Horwitz, E. P.; Schulz, W. W.

    1998-06-18

    During the last 15 years, a number of solvent extraction/recovery processes have been developed for the removal of the transuranic elements, {sup 90}Sr and {sup 137}Cs from acidic high-level liquid waste. These processes are based on the use of a variety of both acidic and neutral extractants. This chapter will present an overview and analysis of the various extractants and flowsheets developed to treat acidic high-level liquid waste streams. The advantages and disadvantages of each extractant along with comparisons of the individual systems are discussed.

  8. Separation of zirconium and hafnium by solvent extraction using mixture of TBP and Cyanex 923

    Energy Technology Data Exchange (ETDEWEB)

    Taghizadeh, M., E-mail: mtaghizadeh@aeoi.org.ir [Nuclear Fuel Cycle Research School, Nuclear Science and Technology Research Institute, End of North Karegar Ave., P.O. Box 14395-836, Tehran (Iran, Islamic Republic of); Ghanadi, M.; Zolfonoun, E. [Nuclear Fuel Cycle Research School, Nuclear Science and Technology Research Institute, End of North Karegar Ave., P.O. Box 14395-836, Tehran (Iran, Islamic Republic of)

    2011-05-31

    In this study, a new Zr/Hf separation procedure by solvent extraction is proposed. The method is based on using the mixture of TBP and Cyanex 923 as extractant in the organic phase. Several parameters including; TBP/Cyanex 923 volume ratio, extractant concentration in the organic phase, nitric acid and NaNO{sub 3} concentration in aqueous phase have been investigated. The results demonstrate better condition respect to traditional TBP/HNO{sub 3} process. Lower required acid concentration and more zirconium extraction are some advantages of the new separation process.

  9. Separation of zirconium and hafnium by solvent extraction using mixture of TBP and Cyanex 923

    Science.gov (United States)

    Taghizadeh, M.; Ghanadi, M.; Zolfonoun, E.

    2011-05-01

    In this study, a new Zr/Hf separation procedure by solvent extraction is proposed. The method is based on using the mixture of TBP and Cyanex 923 as extractant in the organic phase. Several parameters including; TBP/Cyanex 923 volume ratio, extractant concentration in the organic phase, nitric acid and NaNO 3 concentration in aqueous phase have been investigated. The results demonstrate better condition respect to traditional TBP/HNO 3 process. Lower required acid concentration and more zirconium extraction are some advantages of the new separation process.

  10. Extraction of phenols from lignin microwave-pyrolysis oil using a switchable hydrophilicity solvent.

    Science.gov (United States)

    Fu, Dongbao; Farag, Sherif; Chaouki, Jamal; Jessop, Philip G

    2014-02-01

    Microwave pyrolysis of lignin, an aromatic polymer byproduct from paper-pulping industry, produces char, gases, and lignin pyrolysis oil. Within the oil are valuable phenolic compounds such as phenol, guaiacol and catechol. In this work, we describe a method using switchable hydrophilicity solvents (SHS) to extract phenols as a mixture from lignin microwave-pyrolysis oil at the scale of 10 g of bio-oil. Even at this small scale, losses are small; 96% of the bio-oil was recovered in its three fractions, 72% of guaiacol and 70% of 4-methylguaiacol, the most abundant phenols in the bio-oil, were extracted and 91% of the solvent SHS was recovered after extraction. The starting material (lignin microwave-pyrolysis oil) and the three fractions resulted from SHS extraction were characterized by GC-MS and quantitative (13)C{(1)H} and (31)P{(1)H} NMR spectroscopy. Copyright © 2013 Elsevier Ltd. All rights reserved.

  11. Analysis of continuous solvent extraction of nickel from spent electroless nickel plating baths by a mixer-settler.

    Science.gov (United States)

    Huang, Ying; Tanaka, Mikiya

    2009-05-30

    It is urgent to develop an effective technique to treat the large amount of spent electroless nickel plating bath and recycle the high concentration nickel. In our previous study, high recycling efficiency of nickel from the model spent bath was obtained by continuous solvent extraction with 2-hydroxy-5-nonylacetophenone oxime (LIX84I) as the extractant and 2-ethylhexylphosphonic acid mono-2-ethylhexyl ester (PC88A) as the accelerator using a mixer-settler extractor. It was observed that the extraction efficiency was affected by the operation parameters such as the flow rates of the aqueous and organic phases and the total stage number. In the present study, the effects of the operation parameters on the extraction efficiency were quantitatively studied on the basis of the pseudo-first-order interfacial extraction rate equation together with the hydrodynamic properties in the mixer. The organic phase holdup, measured under varying conditions of the flow rates of both phases, was analyzed by the Takahashi-Takeuchi holdup model in order to estimate the specific interfacial area. The overall extraction rate coefficients defined by the product of the interfacial extraction rate constant and the specific interfacial area were evaluated using the experimental data and ranged from 3.5 x 10(-3) to 6.7 x 10(-3)s(-1), which was close to the value of 3.4 x 10(-3)s(-1) obtained by batch extraction. Finally, an engineering simulation method was established for assessing the extraction efficiency of nickel during a multistage operation.

  12. Recombinant human proinsulin from transgenic corn endosperm: solvent screening and extraction studies

    Directory of Open Access Journals (Sweden)

    C. S. Farinas

    2007-09-01

    Full Text Available Recombinant pharmaceutical proteins are being produced in different systems such as bacteria and mammalian cell cultures. The use of transgenic plants as bioreactors has recently arisen as an alternative system offering many practical and economic advantages. However, finding an optimum strategy for the downstream processing (DSP of recombinant proteins from plants still remains a challenge. In this work, we studied the extraction of recombinant human proinsulin (rhProinsulin produced in the endosperm of transgenic corn seeds. An efficient extraction solvent was selected and the effects of temperature, solvent-to-solid ratio, time, and impeller rotational speed on the extraction were evaluated using an experimental design. After an extraction kinetics study, temperature was further evaluated to maximize rhProinsulin concentration in the extracts and to minimize the native corn components carbohydrates, phenolic compounds, and proteins. A high efficiency condition for extracting rhProinsulin with the selected solvent - 50 mM sodium bicarbonate buffer pH 10.0 and 5 mM DTT - was an extraction time of 2 h at a solvent-to-solid ratio of 10:1 and 25º C. The maximum rhProinsulin concentration in the extracts at that condition was 18.87 mg l-1 or 0.42% of the total soluble protein. These values are within the range in which the production of pharmaceutical proteins in plants can be competitive with other expression systems. The results presented provide information for the development of an additional production platform for the hormone insulin.

  13. Determination of Uranium in Apatite Minerals by Solvent Extraction--Inductively Coupled Plasma Atomic Emission Spectrometry

    OpenAIRE

    1993-01-01

    [Abstract] Solvent, extraction-ICP atomic emission spectrometry was applied to the determination of uranium in apatite minerals. Apatite minerals were treated with nitric acid. After removing a small quantity of insoluble residue, uranium was extracted with 0.05 mol/dm^3 1-phonyl-3-mcthyl-4-trifluoroacetyl-5-pyrazolonc-diisobutyl kctone at pH 0.8. The uranium content in the apatite was found to be (20.3〜132.9)×10^%.

  14. Effects of Ultrasound Power, Temperature and Flow Rate of Solvent on Decontamination of Sensitive Equipment by Extraction

    Directory of Open Access Journals (Sweden)

    Marek Andrle

    2014-03-01

    Full Text Available The solvent extraction process is regarded amongst other known methods to be applicable for decontamination of sensitive equipment components, especially in cases the components are contaminated in-depth with chemical warfare agents. Viability of the solvent extraction method was evaluated on coupons of butadiene rubber contaminated by sulphur mustard before decontamination by the solvent extraction. The contaminated coupons were extracted in a flow cell, which the solvent (ethoxynonafluorobutane passed through. Three following specific operational factors, namely the temperature, the flow rate, and the power of ultrasound bath, were assessed for the extent of influencing upon the respective observed extraction efficiencies. The paper describes the results of the evaluation of the solvent extraction effectiveness.Defence Science Journal, 2014, 64(2, pp. 168-172. DOI: http://dx.doi.org/10.14429/dsj.64.3887

  15. Screening of TODGA/TBP/OK solvent mixtures for the grouped extraction of actinides

    Energy Technology Data Exchange (ETDEWEB)

    Brown, Jamie; Carrott, Michael J; Maher, Chris J; Mason, Chris; McLachlan, Fiona; Sarsfield, Mark J; Taylor, Robin J; Woodhead, Dave A [National Nuclear Laboratory, B170, Sellafield, Seascale, CUMBRIA, CA20 1PG (United Kingdom); Fox, O Danny, E-mail: mark.sarsfield@nnl.co.uk [Nuclear Decommissioning Authority, Herdus House, Westlakes Science and Technology Park, Moor Row, CA24 3HU (United Kingdom)

    2010-03-15

    The solvent combination N,N,N'N'- tetraoctyl diglycolamide (TODGA)/tributyl phosphate (TBP)/odourless kerosene (OK) is examined as a potential solvent system for a Grouped Actinide Extraction (GANEX) process to separate all of the actinides from fission products when reprocessing spent nuclear fuel. A series of solvent extraction batch experiments were performed with a range of TODGA/TBP/OK solvent combinations to assess the sensitivity of distribution values for a number of key elements towards [TBP] (0 - 1.1M), [TODGA] (0.1-0.4M), [HNO{sub 3}] (0.1-5M) and heavy metal loading ([U] 0-200g/l). There is little impact on D{sub Am} or D{sub Eu} across the solvent range and no influence from U loading. Excellent D{sub Np} values (> 10) are observed, increasing with increasing [TODGA], with [TBP] having little influence. Such high D{sub Np} values may obviate the need for preconditioning of dissolved fuel feeds to control Np routing. High D{sub Tc} values are found even at 5M HNO{sub 3}, therefore Tc is expected to remain in the solvent phase. Both Pu(III) and Pu(IV) are readily extracted with D{sub Pu(III)} > D{sub Pu(IV)}. Uranium is extracted by both TBP and TODGA and TBP is shown to effectively compete with TODGA for uranium coordination sites. Third phase formation occurs at high [U] loading and [HNO{sub 3}] but is suppressed by increasing [TBP].

  16. Impurity Distribution Behavior in Caprolactam Extraction with Environmentally Benign Mixed Solvents

    NARCIS (Netherlands)

    Delden, van M.L.; Drumm, C.; Kuipers, N.J.M.; Haan, de A.B.

    2006-01-01

    In a previous study a solvent mixture of heptane containing 40 mass % heptanol was selected as an alternative in the industrial extraction of caprolactam to replace benzene, toluene, or chlorinated hydrocarbons. This work reports the equilibrium distribution ratio of caprolactam and four model impur

  17. Solvent extraction as additional purification method for postconsumer plastic packaging waste

    NARCIS (Netherlands)

    Thoden van Velzen, E.U.; Jansen, M.

    2011-01-01

    An existing solvent extraction process currently used to convert lightly polluted post-industrial packaging waste into high quality re-granulates was tested under laboratory conditions with highly polluted post-consumer packaging waste originating from municipal solid refuse waste. The objective was

  18. Extraction of polycyclic aromatic hydrocarbons from soot and sediment : solvent selection and implications for sorption mechanism

    NARCIS (Netherlands)

    Jonker, M.T.O.; Koelmans, A.A.

    2002-01-01

    Soot contains high levels of toxic compounds such as polycyclic aromatic hydrocarbons (PAHs). Extraction of PAHs from soot for quantitative analysis is difficult because the compounds are extremely tightly bound to the sorbent matrix. This study was designed to investigate the effect of solvent type

  19. Fractionation of five technical lignins by selective extraction in green solvents and characterization of isolated fractions

    NARCIS (Netherlands)

    Boeriu, C.G.; Fitigau, F.; Gosselink, R.J.A.; Frissen, A.E.; Stoutjesdijk, J.H.; Peter, F.

    2014-01-01

    Lignins from softwood, hardwood, grass and wheat straw were fractionated by selective extraction at ambient temperature using green solvents like acetone/water solutions of 10, 30, 50, 70 and 90% (v/v) acetone and ethyl acetate. A comparison between the isolated fractions and unfractionated lignins

  20. Solvent extraction as additional purification method for postconsumer plastic packaging waste

    NARCIS (Netherlands)

    Thoden van Velzen, E.U.; Jansen, M.

    2011-01-01

    An existing solvent extraction process currently used to convert lightly polluted post-industrial packaging waste into high quality re-granulates was tested under laboratory conditions with highly polluted post-consumer packaging waste originating from municipal solid refuse waste. The objective was

  1. Chemical profiling of Centella asiatica under different extraction solvents and its antibacterial activity, antioxidant activity

    Directory of Open Access Journals (Sweden)

    Supawan Rattanakom

    2015-12-01

    Full Text Available Centella asiatica (L urban, synonym Hydrocotyle asiatica, is found almost all over the world. This plant is famous in Ayurvedic medicine and used in the management of central nervous system, skin and gastrointestinal disorder. Thus this research had been done to evaluate the effect of solvent extraction (Ethanol, Chloroform and Hexane of C. asiatica on chemical profile, antioxidant activity and antibacterial activity against some foodborne pathogens. The result showed that all solvents (ethanol, chloroform and hexane used in extraction showed antibacterial activity against Salmonella enterica Typhimurium U302, S. enterica Enteritidis, S. enterica 4,5,12:I human (US clone, Bacillus cereus and B. subtilis at 50mg/ml concentration. In antioxidant part, ethanolic extract gave highest phenolic content and FRAP value. The results also showed that different extraction solvent gave different chemical profile. Hexane extract C. asiatica showed lowest in both antibacterial and antioxidant activity. Ethanolic and chloroform extract of C. asiatica showed promising potential in both antibacterial and antioxidant activity.

  2. Effect of different solvents on extraction of phenolic compounds and antioxidant activity of hawthorn (Crataegus orientalis fruits

    Directory of Open Access Journals (Sweden)

    Hacer ÇOKLAR

    2016-12-01

    Full Text Available Extraction of bio compounds from plant materials is one of the most important step of the processes such as dietary supplement production and recovery of the compounds from the industrial wastes. It is highly affected from the factors such as solvent type, particle size, extraction time and temperature. To determine the total phenolics, individual phenolic profile and antioxidant activity of Hawthorn (Crataegus orientalis fruit extracted with different solvents and to specify the best solvent for extraction of phenolics were aimed in this research. Fruits, picked from wild growing trees in Beyşehir, were extracted with water, methanol and methanol:water (1:1 mixture. Highest total phenolics and antioxidant activity were observed in methanol:water extract. While gallic acid was extracted effectively in water, methanol:water mixture was the best solvent for extraction of procyanidin B1, procyanidin B2, (-- epicatechin, epigallocatechin gallate and rutin.

  3. Mechanism of gold solvent extraction from aurocyanide solution by quaternary amines: models of extracting species based on hydrogen bonding

    Institute of Scientific and Technical Information of China (English)

    马刚; 闫文飞; 陈景; 严纯华; 高宏成; 周维金; 施鼐; 吴谨光; 徐光宪; 黄昆; 余建民; 崔宁

    2000-01-01

    The mechanism of gold solvent extraction from KAu(CN)2 solution was investigated by means of FTIR, EXAFS, ICP and radioactive tracer methods. Two extraction systems were studied, namely N263-tributyl phosphate(TBP)-n-dodecane and N263-iso-octanol-n-dodecane. High-resolution FT IR spectroscopy indicated that the CN stretching vibrations of the two extraction systems differred greatly. In order to interpret the significant difference in CN stretching vibrations, twoextracting species models are proposed——supramolecular structures based on the formation ofhydrogen bonds between Au(CN)2- and modifiers such as TBP and iso-octanol.

  4. Influence of the amine salt anion on the synergic solvent extraction of praseodymium with mixtures of chelating extractants and tridodecylamine

    Energy Technology Data Exchange (ETDEWEB)

    Dukov, I.L.; Jordanov, V.M. [Higher Inst. of Chemical Technology, Sofia (Bulgaria)

    1995-11-01

    The solvent extraction of Pr with thenoyltrifluoroacetone, (HTTA) or 1-phenyl-3-methyl-4-benzoyl-pyrazol-5-one(HP) and tridodecylammonium salt (TDAHA,A{sup -} = Cl{sup -},NO{sub 3}{sup -}, ClO{sub 4}{sup -}) in C{sub 6}H{sub 6} has been studied. The composition of the extracted species has been determined as Pr(TTA){sub 3} TDAHA and TDAH{sup +}[PrP{sub 4}]{sup -}. The values of the equilibrium constants, have been calculated. The extraction mechanism has been discussed on the basis of the experimental data. 34 refs., 6 figs., 2 tabs.

  5. Ohmic heating as a pre-treatment in solvent extraction of rice bran.

    Science.gov (United States)

    Nair, Gopu Raveendran; Divya, V R; Prasannan, Liji; Habeeba, V; Prince, M V; Raghavan, G S V

    2014-10-01

    Rice bran, which is one of the major by products of paddy contain high quality proteins and edible oil apart from fibre, ash and NFE (nitrogen free extract). The existing solvent extraction method employs n-hexane as the most viable solvent for the extraction of oil from rice bran. But the high cost and scarce availability of n-hexane resulted in uneconomical extraction of rice bran oil. In this study, rice bran was ohmically heated for different time periods(1, 2 and 3 min) with different current values (5, 15 and 20 A) and with different concentration of sodium chloride (1 M, 0.1 M and 0.01 M) as conducting medium. The ohmically heated rice bran was subjected to extraction studies. Ohmic heating of rice bran of paddy varieties Red Triveni and Basmati reduced the extraction time by nearly 75 % and 70 % respectively and gave a maximum quantity of oil extracted when compared to bran, which was not ohmically heated. From the experiments with varying concentrations, residence time of ohmic heating and currents, it was found that ohmically heating the rice bran with 1 M sodium chloride solution and with a current value of 20 A for 3 min gave maximum oil extraction with minimum extraction time.

  6. Computer-aided molecular design of solvents for accelerated reaction kinetics.

    Science.gov (United States)

    Struebing, Heiko; Ganase, Zara; Karamertzanis, Panagiotis G; Siougkrou, Eirini; Haycock, Peter; Piccione, Patrick M; Armstrong, Alan; Galindo, Amparo; Adjiman, Claire S

    2013-11-01

    Solvents can significantly alter the rates and selectivity of liquid-phase organic reactions, often hindering the development of new synthetic routes or, if chosen wisely, facilitating routes by improving rates and selectivities. To address this challenge, a systematic methodology is proposed that quickly identifies improved reaction solvents by combining quantum mechanical computations of the reaction rate constant in a few solvents with a computer-aided molecular design (CAMD) procedure. The approach allows the identification of a high-performance solvent within a very large set of possible molecules. The validity of our CAMD approach is demonstrated through application to a classical nucleophilic substitution reaction for the study of solvent effects, the Menschutkin reaction. The results were validated successfully by in situ kinetic experiments. A space of 1,341 solvents was explored in silico, but required quantum-mechanical calculations of the rate constant in only nine solvents, and uncovered a solvent that increases the rate constant by 40%.

  7. Flavonoid compositions and antioxidant activity of calamondin extracts prepared using different solvents

    Directory of Open Access Journals (Sweden)

    Shyi-Neng Lou

    2014-09-01

    Full Text Available Calamondin has been demonstrated to exhibit antioxidant function and tyrosinase inhibitory activity, which might be attributed to its flavonoid compounds. To improve their application, the flavonoid compositions and antioxidant activity of calamondin extracts, prepared by different solvents, were investigated. The results showed that total phenolic and flavonoid contents of extracts from peel of calamondin were higher than that from pulp, except the flavonoid content in hot water extract. The flavonoids found in extracts of calamondin were 3′,5′-di-C-β-glucopyranosylphloretin (DGPP, naringin, hesperidin, nobiletin, tangeretin, and diosmin. DGPP exhibited the highest quantity, while naringin and hesperidin were the other two major flavonoids. The content of DGPP in hot water extract of peel was higher than in extracts of organic solvents, however, the contents of nobiletin and tangeretin were found only in extracts of organic solvents. The highest levels of total flavonoids and DGPP were obtained in hot water extract from peel at 90°C. The extracts of hot water and ethyl acetate showed higher 2,2-diphenyl-1-picrylhydrazyl (DPPH radical scavenging potency than that of ethanol and methanol. A positive relationship existed between total phenolic contents and DPPH scavenging potency (p < 0.01, while total flavonoid compositions also showed correlation (p < 0.05. Thus, DGPP, naringin, and hesperidin might contribute to antioxidant activity. Collectively, the hot water extract of calamondin peel might have potential for health food and cosmetic applications due to its good antioxidant activity and high level of DGPP.

  8. Successive solvent extraction and free radical scavenging activity of Azadirachta indica A. juss

    Directory of Open Access Journals (Sweden)

    Mohammed Ibrahim

    2012-01-01

    Full Text Available Background: Plant-based or plant-derived drugs occupied 30% of the modern system of medicine. Several trees possess a variety of biologically active compounds. Among them, Azadirachta indica, belonging to the family Meliaceae, plays a vital role as it acts as nature′s pharmacy from several centuries of time. In the path of searching for potential antioxidants from plant origin, different parts of Azadirachta indica have been selected. Aim: Successive solvent extracts of leaves, seeds and root barks of Azadirachta indica A. Juss (neem were studied for their free radical scavenging activity. Materials and Methods: Extraction capacity of different solvents based on their polarity order was compared and the extracts were subjected to 1-diphenyl-2-picryl hydrazyl (DPPH free radical scavenging assay. Statistical Analysis: All values were expressed in mean±SEM and correlation coefficient (R 2 values obtained from dose response curves were expressed for antioxidant results. Results: The results showed that the highest yields was found with the hydroalcoholic extract of leaves, followed by the hydroalcoholic extract of seeds and methanolic extracts of leaves and seeds, respectively. Free radical scavenging activity of various extracts was determined by measuring 1, DPPH free radical scavenging activity. The results were expressed in terms of IC 50 values. The root bark methanol extract was found to exhibit the highest IC 50 of 14.82-μg/mL at the concentration of 25-μg/mL. Conclusion: It is concluded that hydroalcohol and methanol are the best solvents to extract the antioxidant compounds from Azadirachta indica. The root bark methanolic extract was found to have the highest free radical scavenging potential against DPPH radical.

  9. Comparative analysis of essential oil composition of Iranian and Indian Nigella sativa L. extracted using supercritical fluid extraction and solvent extraction.

    Science.gov (United States)

    Ghahramanloo, Kourosh Hasanzadeh; Kamalidehghan, Behnam; Akbari Javar, Hamid; Teguh Widodo, Riyanto; Majidzadeh, Keivan; Noordin, Mohamed Ibrahim

    2017-01-01

    The objective of this study was to compare the oil extraction yield and essential oil composition of Indian and Iranian Nigella sativa L. extracted by using Supercritical Fluid Extraction (SFE) and solvent extraction methods. In this study, a gas chromatography equipped with a mass spectrophotometer detector was employed for qualitative analysis of the essential oil composition of Indian and Iranian N. sativa L. The results indicated that the main fatty acid composition identified in the essential oils extracted by using SFE and solvent extraction were linoleic acid (22.4%-61.85%) and oleic acid (1.64%-18.97%). Thymoquinone (0.72%-21.03%) was found to be the major volatile compound in the extracted N. sativa oil. It was observed that the oil extraction efficiency obtained from SFE was significantly (Pextraction technique. The present study showed that SFE can be used as a more efficient technique for extraction of N. Sativa L. essential oil, which is composed of higher linoleic acid and thymoquinone contents compared to the essential oil obtained by the solvent extraction technique.

  10. Determination of extractability of pine bark using supercritical CO(2) extraction and different solvents: optimization and prediction.

    Science.gov (United States)

    Yesil-Celiktas, Ozlem; Otto, Frank; Gruener, Sabine; Parlar, Harun

    2009-01-28

    Bark from Pinus brutia was extracted with supercritical fluid extraction (SFE), using CO(2), at various extraction conditions both at laboratory and at pilot scale. Optimized parameters were 200 bar, 60 degrees C, and 3% ethanol at a solvent/feed ratio of 30. Additionally, the pine bark was sonicated (1 h at 50 degrees C) by different solvents (n-hexane, dichloromethane, ethyl acetate, and ethanol) to investigate the correlation between the different extraction setups and to obtain information on SFE up-scaling possibilities. Analyzed by HPLC, 7.2% of (-)-catechin was extractable at laboratory scale, and 58.4% (800 bar) and 47.8% (200 bar), both with modifiers, at pilot scale. By sonication with ethanol, 46.8% of (-)-catechin and almost 100% of (-)-epicatechin and (-)-catechin gallate were extracted. Ethyl acetate extract revealed high correlations with the laboratory scale SFE (r = 0.98) and also pilot scale SFE runs at 200 (r = 0.99) and 800 bar (r = 0.98) without modifiers.

  11. Caustic-Side Solvent Extraction Chemical and Physical Properties Progress in FY 2000 and FY 2001.

    Energy Technology Data Exchange (ETDEWEB)

    Moyer, BA

    2002-04-17

    The purpose of this work was to provide chemical- and physical-property data addressing the technical risks of the Caustic-Side Solvent Extraction (CSSX) process as applied specifically to the removal of cesium from alkaline high-level salt waste stored at the US Department of Energy Savannah River Site. As part of the overall Salt Processing Project, this effort supported decision-making in regards to selecting a preferred technology among three alternatives: (1) CSSX, (2) nonelutable ion-exchange with an inorganic silicotitanate material and (3) precipitation with tetraphenylborate. High risks, innate to CSSX, that needed specific attention included: (1) chemical stability of the solvent matrix, (2) radiolytic stability of the solvent matrix, (3) proof-of-concept performance of the proposed process flowsheet with simulated waste, and (4) performance of the CSSX flowsheet with actual SRS high-level waste. This body of work directly addressed the chemical-stability risk and additionally provided supporting information that served to plan, carry out, and evaluate experiments conducted by other CSSX investigators addressing the other high risks. Information on cesium distribution in extraction, scrubbing, and stripping served as input for flowsheet design, provided a baseline for evaluating solvent performance under numerous stresses, and contributed to a broad understanding of the effects of expected process variables. In parallel, other measurements were directed toward learning how other system components distribute in the flowsheet. Such components include the solvent components themselves, constituents of the waste, and solvent-degradation products. Upon understanding which components influence flowsheet performance, it was then possible to address in a rational fashion how to clean up the solvent and maintain its stable function.

  12. Pulsed electric field (PEF) as an intensification pretreatment for greener solvent lipid extraction from microalgae.

    Science.gov (United States)

    Zbinden, Mauricio D Antezana; Sturm, Belinda S M; Nord, Ryan D; Carey, William J; Moore, David; Shinogle, Heather; Stagg-Williams, Susan M

    2013-06-01

    Microalgae, with their high lipid content, are a promising feedstock for renewable fuels. Traditionally, human and environmentally toxic solvents have been used to extract these lipids, diminishing the sustainability of this process. Herein, pulsed electric field technology was utilized as a process intensification strategy to enhance lipid extraction from Ankistrodesmus falcatus wet biomass using the green solvent, ethyl acetate. The extraction efficiency for ethyl acetate without PEF was lower (83-88%) than chloroform. In addition, the ethyl acetate exhibited a 2-h induction period, while the chloroform showed no time dependence. Utilizing PEF technology resulted in 90% of the cells being lysed and a significant enhancement in the rate of lipid recovery using ethyl acetate. The increase in lipid recovery was due to the presence of the electric field and not due to temperature effects. The PEF technology uses less energy than other PEF systems reported in the literature.

  13. THE INFLUENCE OF TIME AND TYPE OF SOLVENT ON EFFICIENCY OF THE EXTRACTION OF POLYPHENOLS FROM GREEN TEA AND ANTIOXIDANT PROPERTIES OBTAINED EXTRACTS

    OpenAIRE

    Beata Drużyńska; Agnieszka Stępniewska; Rafał Wołosiak

    2007-01-01

    The aim of the study was to investigate the influence of the type of solvent and time on efficiency of the extraction of polyphenols and antioxidant properties extracts obtained from green tea. Extraction was conducted at room temperature using four solvents: water and 80% ethanol, 80% methanol and 80% acetone (water solutions, v/v) at 15, 30 and 60 minutes. Extracts were analysed for contents of polyphenols and catechins. The antioxidant properties have been determined by two methods: scaven...

  14. Efficient Extraction of Astaxanthin from Phaffia rhodozyma with Polar and Non-polar Solvents after Acid Washing

    Institute of Scientific and Technical Information of China (English)

    YIN Chunhua; YANG Shuzhen; LIU Xiaolu; YAN Hai

    2013-01-01

    method of extracting astaxanthin from Phaffia rhodozyma with various solvents after acid washing was investigated.The extraction efficiency was distinctly increased after acid washing of P.rhodozyma cells.When the concentration of HCl was 0.4 mol·L-,the highest extraction efficiency of astaxanthin was achieved which was about three times higher than the control.Acetone or benzene as single polar or non-polar solvent was the most effective solvent in our research.With a combination of isopropanol and n-hexane (volume ratio of 2 ∶ 1),the maximal extraction efficiency was achieved,approximately 60% higher than that obtained with a single solvent.The liquid-solid ratio and the extracting time were also optimized.Under the optimum extraction conditions,the extraction yield of astaxanthin exceeded 98%.

  15. Combining Solvent Extraction and Bioremediation for Removing Weathered Petroleum from Contaminated Soil

    Institute of Scientific and Technical Information of China (English)

    WU Guo-Zhong; F.COULON; YANG Yue-Wei; LI Hong; SUI Hong

    2013-01-01

    This study aimed to evaluate the efficacy,practicality and sustainability of a combined approach based on solvent extraction and biodegradation to remediate the soils contaminated with high levels of weathered petroleum hydrocarbons.The soils used in this study were obtained from the Shengli Oilfield in China,which had a long history of contamination with high concentrations of petroleum hydrocarbons.The contaminated soils were washed using a composite organic solvent consisting of hexane and pentane (4:1,v/v) and then bioremediated in microcosms which were bioaugmentated with Bacillus subtilis FQ06 strains and/or rhamnolipid.The optimal solvent extraction conditions were determined as extraction for 20 min at 25 ℃ with solvent-soil ratio of 6:1 (v/w).On this basis,total petroleum hydrocarbon was decreased from 140000 to 14000 mg kg-1,which was further reduced to < 4000 mg kg-1 by subsequent bioremediation for 132 d.Sustainability assessment of this integrated technology showed its good performance for both short-and long-term effectiveness.Overall the results encouraged its application for remediating contaminated sites especially with high concentration weathered hydrocarbons.

  16. Choice of solvent extraction technique affects fatty acid composition of pistachio (Pistacia vera L.) oil.

    Science.gov (United States)

    Abdolshahi, Anna; Majd, Mojtaba Heydari; Rad, Javad Sharifi; Taheri, Mehrdad; Shabani, Aliakbar; Teixeira da Silva, Jaime A

    2015-04-01

    Pistachio (Pistacia vera L.) oil has important nutritional and therapeutic properties because of its high concentration of essential fatty acids. The extraction method used to obtain natural compounds from raw material is critical for product quality, in particular to protect nutritional value. This study compared the fatty acid composition of pistachio oil extracted by two conventional procedures, Soxhlet extraction and maceration, analyzed by a gas chromatography-flame ionization detector (GC-FID). Four solvents with different polarities were tested: n-hexane (Hx), dichloromethane (DCM), ethyl acetate (EtAc) and ethanol (EtOH). The highest unsaturated fatty acid content (88.493 %) was obtained by Soxhlet extraction with EtAc. The Soxhlet method extracted the most oleic and linolenic acids (51.99 % and 0.385 %, respectively) although a higher concentration (36.32 %) of linoleic acid was extracted by maceration.

  17. Separation and recovery of heavy metals from waste water using synergistic solvent extraction

    Science.gov (United States)

    Li, Yan; Yang, Limei; Xu, Zheng; Sun, Qi

    2017-01-01

    Heavy metal wastewater pollution is one of the three major water pollutions in the world. The zinc hydrometallurgy smelting process usually discharge large quantities of heavy metal wastewater into the environment. In this paper, a synergistic solvent extraction process has been developed to recover copper, nickel, zinc and cadmium respectively from calcium and magnesium. The synergistic organic system contained 0.50 M Versatic 10 and 0.5 M Mextral 984H in DT100. Adjusting pH to 2.0 at 40 °C, the copper will be extracted preferentially with the extraction rate more than 99%. Continuing to adjust pH to 4.2 at 40 °C, the nickel will be extracted secondly with an extraction rate more than 98%; the zinc and cadmium in raffinate could be extracted separately while pH is about 6.5.

  18. Combination pulsed electric field with ethanol solvent for Nannochloropsis sp. extraction

    Science.gov (United States)

    Nafis, Ghazy Ammar; Mumpuni, Perwitasari Yekti; Indarto, Budiman, Arief

    2015-12-01

    Nowadays, energy is one of human basic needs. As the human population increased, energy consumption also increased. This condition causes energy depletion. In case of the situation, alternative energy is needed to replace existing energy. Microalgae is chosen to become one of renewable energy resource, especially biodiesel, because it contains high amount of lipid instead of other feedstock which usually used. Fortunately, Indonesia has large area of water and high intensity of sunlight so microalgae cultivation becomes easier. Nannochloropsis sp., one of microalgae species, becomes the main focus because of its high lipid content. Many ways to break the cell wall of microalgae so the lipid content inside the microalgae will be released, for example conventional extraction, ultrasonic wave extraction, pressing, and electrical method. The most effective way for extraction is electrical method such as pulsed electric field method (PEF). The principal work of this method is by draining the electrical current into parallel plate. Parallel plate will generate the electrical field to break microalgae cell wall and the lipid will be released. The aim of this work is to evaluate two-stage procedure for extraction of useful components from microalgae Nannochloropsis sp. The first stage of this procedure includes pre-treatment of microalgae by ethanol solvent extraction and the second stage applies the PEF extraction using a binary mixture of water and ethanol solvent. Ethanol is chosen as solvent because it's safer to be used and easier to be handled than other solvent. Some variables that used to study the most effective operation conditions are frequency and duty cycle for microalgae. The optimum condition based on this research are at frequency 1 Hz and duty cycle 13%.

  19. Magnetic solid-phase extraction of protein with deep eutectic solvent immobilized magnetic graphene oxide nanoparticles.

    Science.gov (United States)

    Xu, Kaijia; Wang, Yuzhi; Ding, Xueqin; Huang, Yanhua; Li, Na; Wen, Qian

    2016-01-01

    As a new type of green solvent, four kinds of choline chloride (ChCl)-based deep eutectic solvents (DESs) have been synthesized, and then a core-shell structure magnetic graphene oxide (Fe3O4-NH2@GO) nanoparticles have been prepared and coated with the ChCl-based DESs. Magnetic solid-phase extraction (MSPE) based Fe3O4-NH2@GO@DES was studied for the first time for the extraction of proteins. The characteristic results of vibrating sample magnetometer (VSM), X-ray diffraction (XRD), Fourier transform infrared spectrometry (FT-IR), thermal gravimetric analysis (TGA) and field emission scanning electron microscopy (FESEM) indicated the successful preparation of Fe3O4-NH2@GO@DES. The concentrations of proteins in studies were determined by a UV-vis spectrophotometer. The advantages of Fe3O4-NH2@GO@DES in protein extraction were compared with Fe3O4-NH2@GO and Fe3O4-NH2, and Fe3O4-NH2@GO@ChCl-glycerol was selected as the suitable extraction solvent. The influence factors of the extraction process such as the pH value, the temperature, the extraction time, the concentration of protein and the amount of Fe3O4-NH2@GO@ChCl-glycerol were evaluated. Desorption experimental result showed 98.73% of BSA could be eluted from the solid extractant with 0.1 mol/L Na2HPO4 solution contained 1 mol/L NaCl. Besides, the conformation of BSA was not changed during the elution by the investigation of circular dichromism (CD) spectra. Furthermore, the analysis of real sample demonstrated that the prepared magnetic nanoparticles did have extraction ability on proteins in bovine whole blood.

  20. Solvent effects on quantitative analysis of brominated flame retardants with Soxhlet extraction.

    Science.gov (United States)

    Zhong, Yin; Li, Dan; Zhu, Xifen; Huang, Weilin; Peng, Ping'an

    2017-05-18

    Reliable quantifications of brominated flame retardants (BFRs) not only ensure compliance with laws and regulations on the use of BFRs in commercial products, but also is key for accurate risk assessments of BFRs. Acetone is a common solvent widely used in the analytical procedure of BFRs, but our recent study found that acetone can react with some BFRs. It is highly likely that such reactions can negatively affect the quantifications of BFRs in environmental samples. In this study, the effects of acetone on the extraction yields of three representative BFRs [i.e., decabrominated diphenyl ether (decaBDE), hexabromocyclododecane (HBCD) and tetrabromobisphenol A (TBBPA)] were evaluated in the Soxhlet extraction (SE) system. The results showed that acetone-based SE procedure had no measureable effect for the recovery efficiencies of decaBDE but could substantially lower the extraction yields for both TBBPA and HBCD. After 24 h of extraction, the recovery efficiencies of TBBPA and HBCD by SE were 93 and 78% with acetone, 47 and 70% with 3:1 acetone:n-hexane, and 82 and 94% with 1:1 acetone:n-hexane, respectively. After 72 h of extraction, the extraction efficiencies of TBBPA and HBCD decreased to 68 and 55% with acetone, 0 and 5% with 3:1 acetone/n-hexane mixtures, and 0 and 13% with 1:1 acetone/n-hexane mixtures, respectively. The study suggested that the use of acetone alone or acetone-based mixtures should be restricted in the quantitative analysis of HBCD and TBBPA. We further evaluated nine alternative solvents for the extraction of the three BFRs. The result showed that diethyl ether might be reactive with HBCD and may not be considered as the alternative to acetone used solvents for the extraction of HBCD.

  1. Evaluation of antimicrobial and antioxidant activities of solvent extracts of Anacyclus pyrethrum L., from Algeria

    Directory of Open Access Journals (Sweden)

    Mohammed El Amine Dib

    2012-11-01

    Full Text Available In the present study, solvent extracts from aerial parts of Anacyclus pyrethrum L. were assessed for their total phenol content, antimicrobial and antioxidant (1,1-diphenyl-2-picrylhydrazyl free radical scavenging and ferric-ion reducing power activities. The amounts of total phenolics and flavonoids in the solvent extracts were determined spectrometrically. (310.78 mg GA/g extract and antioxidant activity (IC50 = 0.056 mg/mL. Increasing the concentration of the extracts resulted in increased ferric reducing antioxidant power for both extracts tested. The methanolic extract exhibited the best antimicrobial activity against three gram-positive bacterium (Listeria monocytogenes: 100%, Bacillus. cereus: 69% and Staphylococcus aureus: 66%, as well as against Candida albicans (81%. Finally, a relationship was observed between the biological activities potential and total phenolic and flavonoid levels of the extract. The results of this study provided an alternative of utilising Anacyclus pyrethrumaerial parts as readily accessible source of natural antioxidant in food cosmetic and pharmaceutical industry

  2. Extraction of garlic with supercritical CO2 and conventional organic solvents

    Directory of Open Access Journals (Sweden)

    J. M. del Valle

    2008-09-01

    Full Text Available Garlic (Allium sativum L. and garlic extracts have therapeutical properties that stem from their sulfur-containing compounds, mainly allicin. The main objective of this work was to compare conventional and "premium" garlic extracts in terms of yield and quality, with the latter being obtained using supercritical carbon dioxide (SC-CO2 as the solvent. Yield ranged between 0.65 and 1.0% and increased with extraction pressure (150-400 bar at a constant temperature of 50°C. Extraction temperature (35-60°C, on the other hand, had little effect at a constant pressure of 300 bar. Based on yield and quality considerations, the best extraction conditions using SC-CO2 were 35-50°C and 300-400 bar. A yield of 5.5% was obtained by conventional extraction using ethanol as the solvent, but ethanol appeared to be less selective for valuable components than SC-CO2. The use of fresh garlic resulted in extracts that more closely resembled commercial products, possibly because of thermal and oxidative degradation of valuable microconstituents during drying.

  3. Solvent extraction of copper and zinc from bioleaching solutions with LIX984 and D2EHPA

    Institute of Scientific and Technical Information of China (English)

    LAN Zhuo-yue; HU Yue-hua; LIU Jian-she; WANG Jun

    2005-01-01

    The solvent extraction of copper and zinc from the bioleaching solutions of low-grade sulfide ores with LIX984 and D2EHPA was investigated. The influences of extractant content, aqueous pH value, phase ratio and equilibration time on metals extraction were studied. The results show that LIX984 has a higher selectivity for copper than for iron, zinc and other metals, and has the copper extraction rate above 97%,while the zinc and iron extraction rate is less than 1.6% respectively. Zinc extraction is carried out following the copper extraction from the raffinate. The zinc extraction with di(2-ethylhexyl) phosphoric acid(D2EHPA) is low due to its poor cation exchange. A sodium salt of D2EHPA is used and the zinc extraction rate is enhanced to above 98%. Though iron (Ⅲ) is strongly extracted before the extraction of zinc by D2EHPA, it is difficult to strip iron from the organic phase by sulfuric acid. The zinc stripping rate is above 99% with 100 g/L sulfuric acid, while that of iron is 0.16%. Hence, the separation of zinc from iron can be achieved by the selective stripping.

  4. Study of the separation of zirconium and hafnium from nitric solutions by solvent extraction

    Energy Technology Data Exchange (ETDEWEB)

    Amaral, Janubia Cristina B.S.; Rocha, Laura R.T.; Morais, Carlos Antonio de, E-mail: jcbsa@cdtn.br, E-mail: lrtr@cdtn.br, E-mail: cmorais@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, BH (Brazil)

    2013-07-01

    This paper describes the study of the separation of Zr and Hf in nitric and hydrochloric media by solvent extraction technique. As aqueous phase, solutions prepared from the Zr and Hf hydroxides and the liquor generated from the product of the alkaline fusion of the zircon were used. The content of Zr and Hf in these solutions were 15 g/L and 0.6 g/L Hf respectively, and its acidity was varied between 1.0 and 10 mol/L. The effect of the acid extractants (DEHPA, IONQUEST®801 and CYANEX®272), solvating extractants (TBP and CYANEX®923) and basic extractants (PRIMENE®JTM, ALAMINE®336 and ALIQUAT®336), all of them diluted in dodecane, was investigated. In the solutions of the basic extractants, 5.0% of tridecanol was added as a modifier agent. Among the extractants investigated, the TBP in a nitric medium showed the best performance in the separation of the Zr/Hf. For acid extractants a high extraction was observed, however, with low selectivity. With the basic extractants no metals extraction was observed under the conditions investigated. The best results were obtained with the liquor generated from the product of alkaline fusion of zircon at acidity 7.0 mol/L and nitrate concentration of 9.2 mol/L. Under these conditions an extraction percentage of 91.6% for Zr and of 12.1% for Hf and a separation factor of Zr/Hf of 79.3 was obtained. (author)

  5. The enhancement of antioxidant compounds extracted from Thymus vulgaris using enzymes and the effect of extracting solvent.

    Science.gov (United States)

    Cerda, Alejandra; Martínez, María Eugenia; Soto, Carmen; Poirrier, Paola; Perez-Correa, Jose R; Vergara-Salinas, Jose R; Zúñiga, María Elvira

    2013-08-15

    We evaluate the total phenolic compounds (TPC) content and the antioxidant activity (AA) of extracts obtained from ground fresh thyme (FT) and depleted thyme (DT), a by-product of the process of essential oil extraction. In addition, enzymatic treatments were evaluated to improve the extraction yields of polyphenolic compounds from thyme. Extractions were performed using several solvents as methanol, ethanol, and water. Enzymes were applied prior to extraction or during the extraction process. The best results were obtained using a mixture of methanol and water, resulting in 2790 and 220 mg Gallic acid equivalent (GAE)/L of TPC for FT and DT, respectively. A similar result was observed for AA. With regard to enzymatic treatment, application of Grindamyl CA 150 enzyme as a pre-treatment resulted in the production of an extract from DT with 614 mg TE (trolox equivalent)/L of AA, 70% more than the control, and an AA of 621 mg TE/L (74% more than the control sample) was obtained using Grindamyl CA 150 during the extraction process. These results suggest that enzymatic treatment is an interesting alternative for producing antioxidant extracts from DT.

  6. MODELING OF THE SOLVENT EXTRACTION EQUILIBRIUM OF URANIUM (VI SULFATE WITH ALAMINE 336

    Directory of Open Access Journals (Sweden)

    É. C. Avelar

    Full Text Available Abstract The present study investigated the solvent extraction of uranium from sulfate acid solutions using Alamine 336 as an extractant dissolved in commercial kerosene Exxsol D-100 and 5% v/v of tridecanol as a modifying agent at room temperature (25±2 ºC and an aqueous/organic volumetric ratio of unity. Experiments were carried out at typical concentration levels like those used at the uranium plant of INB (Indústrias Nucleares do Brasil, Brazil. Data fitting using the slope analysis method revealed that uranium is extracted by Alamine 336 as UO2SO4 and UO2(SO422- species, forming (R3NH+2UO2(SO422- in the organic phase; the extraction of the species UO2(SO434- seems improbable for the operating conditions investigated. The extraction of uranium is significantly reduced when the concentrations of sulfate and chloride ions in the aqueous phase are increased.

  7. TIGER2 with solvent energy averaging (TIGER2A): An accelerated sampling method for large molecular systems with explicit representation of solvent.

    Science.gov (United States)

    Li, Xianfeng; Snyder, James A; Stuart, Steven J; Latour, Robert A

    2015-10-14

    The recently developed "temperature intervals with global exchange of replicas" (TIGER2) accelerated sampling method is found to have inaccuracies when applied to systems with explicit solvation. This inaccuracy is due to the energy fluctuations of the solvent, which cause the sampling method to be less sensitive to the energy fluctuations of the solute. In the present work, the problem of the TIGER2 method is addressed in detail and a modification to the sampling method is introduced to correct this problem. The modified method is called "TIGER2 with solvent energy averaging," or TIGER2A. This new method overcomes the sampling problem with the TIGER2 algorithm and is able to closely approximate Boltzmann-weighted sampling of molecular systems with explicit solvation. The difference in performance between the TIGER2 and TIGER2A methods is demonstrated by comparing them against analytical results for simple one-dimensional models, against replica exchange molecular dynamics (REMD) simulations for sampling the conformation of alanine dipeptide and the folding behavior of (AAQAA)3 peptide in aqueous solution, and by comparing their performance in sampling the behavior of hen egg-white lysozyme in aqueous solution. The new TIGER2A method solves the problem caused by solvent energy fluctuations in TIGER2 while maintaining the two important characteristics of TIGER2, i.e., (1) using multiple replicas sampled at different temperature levels to help systems efficiently escape from local potential energy minima and (2) enabling the number of replicas used for a simulation to be independent of the size of the molecular system, thus providing an accelerated sampling method that can be used to efficiently sample systems considered too large for the application of conventional temperature REMD.

  8. Recommended Guanidine Suppressor for the Next-Generation Caustic-Side Solvent Extraction Process

    Energy Technology Data Exchange (ETDEWEB)

    Moyer, Bruce A [ORNL; Delmau, Laetitia Helene [ORNL; Duncan, Nathan C [ORNL; Ensor, Dale [Tennessee Technological University; Hill, Talon G [ORNL; Lee, Denise L [ORNL; Roach, Benjamin D [ORNL; Sloop Jr, Frederick {Fred} V [ORNL; Williams, Neil J [ORNL

    2013-01-01

    The guanidine recommended for the Next-Generation Caustic-Side is N,N ,N -tris(3,7-dimethyloctyl)guanidine (TiDG). Systematic testing has shown that it is significantly more lipophilic than the previously recommended guanidine DCiTG, the active extractant in the commercial guanidine product LIX -79, while not otherwise changing the solvent performance. Previous testing indicated that the extent of partitioning of the DCiTG suppressor to the aqueous strip solution is significantly greater than expected, potentially leading to rapid depletion of the suppressor from the solvent and unwanted organic concentrations in process effluents. Five candidate guanidines were tested as potential replacements for DCiTG. The tests included batch extraction with simulated waste and flowsheet solutions, third-phase formation, emulsion formation, and partition ratios of the guanidine between the solvent and aqueous strip solution. Preliminary results of a thermal stability test of the TiDG solvent at one month duration indicated performance approximately equivalent to DCiTG. Two of the guanidines proved adequate in all respects, and the choice of TiDG was deemed slightly preferable vs the next best guanidine BiTABG.

  9. Response Surface Optimization of Rotenone Using Natural Alcohol-Based Deep Eutectic Solvent as Additive in the Extraction Medium Cocktail

    Directory of Open Access Journals (Sweden)

    Zetty Shafiqa Othman

    2017-01-01

    Full Text Available Rotenone is a biopesticide with an amazing effect on aquatic life and insect pests. In Asia, it can be isolated from Derris species roots (Derris elliptica and Derris malaccensis. The previous study revealed the comparable efficiency of alcohol-based deep eutectic solvent (DES in extracting a high yield of rotenone (isoflavonoid to binary ionic liquid solvent system ([BMIM]OTf and organic solvent (acetone. Therefore, this study intends to analyze the optimum parameters (solvent ratio, extraction time, and agitation rate in extracting the highest yield of rotenone extract at a much lower cost and in a more environmental friendly method by using response surface methodology (RSM based on central composite rotatable design (CCRD. By using RSM, linear polynomial equations were obtained for predicting the concentration and yield of rotenone extracted. The verification experiment confirmed the validity of both of the predicted models. The results revealed that the optimum conditions for solvent ratio, extraction time, and agitation rate were 2 : 8 (DES : acetonitrile, 19.34 hours, and 199.32 rpm, respectively. At the optimum condition of the rotenone extraction process using DES binary solvent system, this resulted in a 3.5-fold increase in a rotenone concentration of 0.49 ± 0.07 mg/ml and yield of 0.35 ± 0.06 (%, w/w as compared to the control extract (acetonitrile only. In fact, the rotenone concentration and yield were significantly influenced by binary solvent ratio and extraction time (P<0.05 but not by means of agitation rate. For that reason, the optimal extraction condition using alcohol-based deep eutectic solvent (DES as a green additive in the extraction medium cocktail has increased the potential of enhancing the rotenone concentration and yield extracted.

  10. Solvent optimization on Taxol extraction from Taxus baccata L., using HPLC and LC-MS

    Directory of Open Access Journals (Sweden)

    H Sadeghi-aliabadi

    2009-10-01

    Full Text Available "nBackground and the purpose of the study: Taxol, a natural antitumor agent, was first isolated from the extract of the bark of Taxus brevifolia Nutt., which is potentially a limited source for Taxol. In the search of an alternative source, optimum and cost benefit extracting solvents, various solvents with different percentage were utilized to extract Taxol from needles of Taxus baccata. "nMethods: One g of the dried needles of Taxus baccata, collected from Torkaman and Noor cities of Iran, was extracted with pure ethanol or acetone and 50% and 20% of ethanol or acetone in water. Solvents were evaporated to dryness and the residues were dissolved in 5 ml of methanol and filtered. To one ml of the filtrate was added 50 μl of cinamyl acetate as the internal standard and 20 μl of the resulting solution was subjected to the HPLC to determine the extraction efficiencies of tested solvents. Five μl of filtrate was also subjected to the LC-MS using water/acetonitrile (10/90 as mobile phase and applying positive electrospray ionization (ESI to identify the authenticity of Taxol. "nResults: Results of this study indicated that Taxol extraction efficiency was enhanced as the percentage of ethanol or acetone was increased. HPLC analysis showed that Taxol could be quantified by UV detection using standard curve. The standard curve covering the concentration ranges of 7.8 - 500 μg/ml was linear (r2= 0.9992 and CV% ranged from 0.52 to 15.36. LC-MS analysis using ESI in positive-ion mode confirmed the authenticity of Taxol (m/z 854; M+H, as well as some adduct ions such as M+Na (m/z 876, M+K (m/z 892 and M+CH3CN+H2O (m/z 913. "nConclusions: The results suggest that 100% acetone is the best solvent for the extraction of Taxol from Taxus baccata needles.

  11. Effect of solvent on the extraction of lanthanides with picrolonic acid

    Energy Technology Data Exchange (ETDEWEB)

    Ali, A.; Saeed, M.M. [Pakistan Institute of Nuclear Science and Technology (PINSTECH), Islamabad (Pakistan). Chemistry Div.; Rehman, H. [Pakistan Institute of Nuclear Science and Technology (PINSTECH), Islamabad (Pakistan). Central Analytical Facility Div.; Anwar, J. [Punjab Univ., Lahore (Pakistan). Inst. of Chemistry

    2010-07-01

    Extraction of Eu(III), Tb(III) and Lu(III), as representatives of lanthanides, has been studied with picrolonic acid [1-p-nitrophenyl-3-methyl-4-nitro-5-pyrazolone (HPA)] as extractant in various solvents such as acetylacetone (ACAC), 1-octanol (ONL), n-hexanol (HNL), 1-butanol (nBNL), 2-butanol (iBNL), cyclohexanone (CHN), n-butyl ether (BE), di(1,2-dichloroethyl)ether (DCEE), diisobutylketone (DIBK), benzene and toluene from aqueous solution of pH 1-2, having ionic strength of 0.01 mol dm{sup -3} (K{sup +}/H{sup +}, Cl{sup -}). The composition of the extracted adduct has been determined as M(PA){sub 3} except in DCEE where it is M(PA){sub 3}.(HPA). Extraction constants (log K{sub ex}) were calculated and on the basis of log K{sub ex}, the role of diluents in the extraction process has been discussed. The solvents with respect to their extractability of the rare earth metal ions can be arranged in the order ACAC > DIBK > BE> DCEE > ONL > HNL > CHN. (orig.)

  12. Extraction of phenolic compounds from virgin olive oil by deep eutectic solvents (DESs).

    Science.gov (United States)

    García, Aránzazu; Rodríguez-Juan, Elisa; Rodríguez-Gutiérrez, Guillermo; Rios, José Julian; Fernández-Bolaños, Juan

    2016-04-15

    Deep eutectic solvents (DESs) are "green" solvents, applied in this study for the extraction of phenolic compounds from virgin olive oil (VOO). Different combinations of DES consisting of choline chloride (ChCl) in various mixing ratios with sugars, alcohols, organic acids, and urea, as well as a mixture of three sugars were used. The yields of the DES extractions were compared with those from conventional 80% (v/v) methanol/water. DES showed a good solubility of phenolic compounds with different polarities. The two most abundant secoiridoid derivatives in olive oil, oleacein and oleocanthal, extracted with ChCl/xylitol and ChCl/1,2-propanediol showed an increase of 20-33% and 67.9-68.3% with respect to conventional extraction, respectively. To our knowledge, this is the first time that phenolic compounds have been extracted from VOO oil using DES. Our results suggest that DES offers an efficient, safe, sustainable, and cost effective alternative to methanol for extraction of bioactive compounds from VOO.

  13. Antifungal activity of extracts from Piper aduncum leaves prepared by different solvents and extraction techniques against dermatophytes Trichophyton rubrum and Trichophyton interdigitale.

    Science.gov (United States)

    Santos, Maximillan Leite; Magalhães, Chaiana Froés; da Rosa, Marcelo Barcellos; de Assis Santos, Daniel; Brasileiro, Beatriz Gonçalves; de Carvalho, Leandro Machado; da Silva, Marcelo Barreto; Zani, Carlos Leomar; de Siqueira, Ezequias Pessoa; Peres, Rodrigo Loreto; Andrade, Anderson Assunção

    2013-12-01

    The effects of different solvents and extraction techniques upon the phytochemical profile and anti-Trichophyton activity of extracts from Piper aduncum leaves were evaluated. Extract done by maceration method with ethanol has higher content of sesquiterpenes and antifungal activity. This extract may be useful as an alternative treatment for dermatophytosis.

  14. Antifungal activity of extracts from Piper aduncum leaves prepared by different solvents and extraction techniques against dermatophytes Trichophyton rubrum and Trichophyton interdigitale

    Directory of Open Access Journals (Sweden)

    Maximillan Leite Santos

    2013-12-01

    Full Text Available The effects of different solvents and extraction techniques upon the phytochemical profile and anti-Trichophyton activity of extracts from Piper aduncum leaves were evaluated. Extract done by maceration method with ethanol has higher content of sesquiterpenes and antifungal activity. This extract may be useful as an alternative treatment for dermatophytosis.

  15. Selection and design of ionic liquids as solvents in extractive distillation and extraction processes

    NARCIS (Netherlands)

    Schuur, B.

    2015-01-01

    Since the late 1990’s there has been a tremendous growth in literature on ionic liquids (ILs) for a broad range of applications, i.e. catalysis, electrolytes for batteries, in solvolysis of biomass, and also in separation technology. ILs can be applied as solvents for absorption (e.g. of CO2), extra

  16. Comparative study on sulphur reduction from heavy petroleum - Solvent extraction and microwave irradiation approach

    Energy Technology Data Exchange (ETDEWEB)

    Mohammed, Abdullahi Dyadya; Isah, Abubakar Garba; Umaru, Musa; Ahmed, Shehu [Department of Chemical Engineering, Federal University of Technology, P.M.B 65, Minna (Nigeria); Abdullahi, Yababa Nma [National Petroleum Investment Management Services (Nigeria National Petroleum Corporation), Lagos (Nigeria)

    2012-07-01

    Sulphur- containing compounds in heavy crude oils are undesirable in refining process as they affect the quality of the final product, cause catalyst poisoning and deactivation in catalytic converters as well as causing corrosion problems in oil pipelines, pumps and refining equipment aside environmental pollution from their combustion and high processing cost. Sulphur reduction has being studied using microwave irradiation set at 300W for 10 and 15minutes and oxidative- solvent extraction method using n- heptane and methanol by 1:1, 1:2 and 1:3 crude- solvent ratios after being oxidized with hydrogen peroxide, H2O2 oxidants. Percentage sulphur removal with n- heptane solvent by 1:1 and 1:2 are 81.73 and 85.47%; but extraction using methanol by different observed ratios gave less sulphur reduction. Indeed when microwave irradiated at 300W for 10 and 15minutes, 53.68 and 78.45% reduction were achieved. This indicates that microwave irradiation had caused oxidation by air in the oven cavity and results to formation of alkyl radicals and sulphoxide from sulphur compound in the petroleum. The prevailing sulphur found in the crude going by FT-IR results is sulphides which oxidized to sulphoxide or sulphones. It is clear that sulphur extraction with heptane is more efficient than microwave irradiation but economically due to demands for solvent and its industrial usage microwave irradiation can serve as alternative substitute for sulphur reduction in petroleum. Sulphur reduction by microwave radiation should be up- scaled from laboratory to a pilot plant without involving extraction column in the refining.

  17. Comparative study on sulphur reduction from heavy petroleum - Solvent extraction and microwave irradiation approach

    Directory of Open Access Journals (Sweden)

    Abdullahi Dyadya Mohammed, Abubakar Garba Isah, Musa Umaru, Shehu Ahmed, Yababa Nma Abdullahi

    2012-01-01

    Full Text Available Sulphur- containing compounds in heavy crude oils are undesirable in refining process as they affect the quality of the final product, cause catalyst poisoning and deactivation in catalytic converters as well as causing corrosion problems in oil pipelines, pumps and refining equipment aside environmental pollution from their combustion and high processing cost. Sulphur reduction has being studied using microwave irradiation set at 300W for 10 and 15minutes and oxidative- solvent extraction method using n- heptane and methanol by 1:1, 1:2 and 1:3 crude- solvent ratios after being oxidized with hydrogen peroxide, H2O2 oxidants. Percentage sulphur removal with n- heptane solvent by 1:1 and 1:2 are 81.73 and 85.47%; but extraction using methanol by different observed ratios gave less sulphur reduction. Indeed when microwave irradiated at 300W for 10 and 15minutes, 53.68 and 78.45% reduction were achieved. This indicates that microwave irradiation had caused oxidation by air in the oven cavity and results to formation of alkyl radicals and sulphoxide from sulphur compound in the petroleum. The prevailing sulphur found in the crude going by FT-IR results is sulphides which oxidized to sulphoxide or sulphones. It is clear that sulphur extraction with heptane is more efficient than microwave irradiation but economically due to demands for solvent and its industrial usage microwave irradiation can serve as alternative substitute for sulphur reduction in petroleum. Sulphur reduction by microwave radiation should be up- scaled from laboratory to a pilot plant without involving extraction column in the refining.

  18. Comparison of Methanol and Tetraglyme as Extraction Solvents for Determination of Volatile Organics in Soil

    Science.gov (United States)

    1987-11-01

    determining volatile organics in soil can be classified into thefollowing groups: 1. Static or dynamic headspace analysis 2. Solvent extraction-direct...methods based on the dynamic headspace method whereby the volatiles are stripped from a soil/water slurry using a conventional purge-and-trap instrument...651. Brazell, R.S. and MP. Maskarinec (1981) Dynamic headspace analysis of solid waste materials. Journal of High Resolution Chromatography and

  19. Extraction of oil from pequi fruit (Caryocar Brasiliense, Camb. using several solvents and their mixtures

    Directory of Open Access Journals (Sweden)

    Antoniassi, R.

    2011-09-01

    Full Text Available In this study, the oil extraction process from pequi pulp using different solvents (hexane, acetone and ethyl alcohol and their mixtures was investigated, using a simplex-centroid design. The extraction occurred at 50°C, under stirring (22 Hz, for 16 hours. The solid-liquid ratio used was 1:10 (w/w. Higher yield values were obtained for extractions with acetone and hexane, especially their mixtures with ethanol. Iodine value, saponification value and refractive index did not differ significantly among the treatments. A higher acid value was obtained for the extraction with ethyl alcohol. Higher carotenoid contents were obtained for the extraction with acetone and ethyl alcohol as pure solvents. The fatty acid profile in the oil fraction of the extracts did not vary among the different types of solvents and their mixtures.En este trabajo fue estudiado el proceso de extracción de aceite de la pulpa de pequi utilizando diferentes disolventes (n-hexano, acetona y etanol y sus mezclas, empleando diseño central simplex. Las extracciones fueron realizadas a 50°C, durante 16 horas de agitación (22 Hz. La proporción sólido:líquido empleada fue 1:10 (p/p. Los mayores rendimientos fueron obtenidos para las extracciones con acetona y con hexano, especialmente cuando fueron mezclados con etanol. El índice de yodo, el índice de saponificación y el índice de refracción no difirieron significativamente entre los tratamientos. Los mayores valores de acidez se obtuvieron en la extracción con etanol. Los mayores contenidos en carotenoides se obtuvieron en las extracciones con acetona y etanol como disolventes puros. El perfil de los ácidos grasos en las fracciones de aceite de los extractos no presentó variación entre los diferentes tipos de disolventes y sus mezclas.

  20. Antibacterial and antioxidant properties of various solvents extracts of Abutilon theophrasti Medic. leaves.

    Science.gov (United States)

    Tian, Chunlian; Yang, Caixia; Zhang, Dexian; Han, Limei; Liu, Yaochuan; Guo, Wenjie; Fan, Ruiming; Liu, Mingchun

    2017-05-01

    This paper described the extraction procedure of six extracts from Abutilon theophrasti Medic. leaves and evaluated antioxidant and antibacterial activity of different extracts by hydroxyl radical, DPPH radical scavenging, broth micro-dilution and agar-well diffusion methods. The six extracts were prepared by the two extraction procedures: (I) water was the extraction solvent; (II) 90% alcohol extract was extracted by petroleum ether, chloroform, ethyl acetate and n-butanol in turn. Extract yields were 7.34%, 7.31%, 0.45%, 0.12%, 2.70% and 5.68% for extract I to VI. It was revealed that the various extracts had effective antibacterial activity against four test strains from Staphylococcus aureus (ATCC 25923), Streptococcus (ATCC 49619), Escherichia coli (ATCC 25922) and Salmonella (ATCC 01303); meanwhile, the six extracts demonstrated potent antioxidant activity, achieved by hydroxyl radical and DPPH radical scavenging assay. Minimum inhibitory concentrations (MICs) for the bacterial species ranged from 2.21 to 539.46 mg/ml, diameter of inhibition zone ranged from 2.08 to 15.05mm. The scavenging •OH and DPPH• rates were 62.37% to 81.86% with the concentration 0.06 to 1.89mg/ml and 37.80% to 81.23% with the concentration 1.07 to 35.52mg/ml. According to the results, these extracts have antioxidant and antibacterial activity. In view of all the facts collectively, the six extracts will become natural and nontoxic antioxidant and antibacterial agent, and be applied in food and pharmaceutical industries for the prevention or treatment caused by microorganisms and free radicals.

  1. Ethanol as a solvent and hot extraction technique preserved the antioxidant properties of tamarind (Tamarindus indica seed

    Directory of Open Access Journals (Sweden)

    Nushrat Yeasmen

    2015-09-01

    Full Text Available The influence of two extraction solvents (ethanol and acetone and two extraction techniques i.e., hot extraction at 400C and cold extraction at 260C were investigated on the phenolic content and antioxidant activity of extracts from Tamarindus indica seed. The antioxidant activity of T. indica was determined by evaluating 1,1-Diphenyl-2-picrylhydrazyl (DPPH scavenging activity, ferric reducing power assay (FRAP and ascorbic acid equivalent content (AAC. The tested sample showed appreciable amounts of total phenolic contents (51.45-71.68 mg GAE/gm of dry extract, DPPH scavenging capacity (61.18-71.17%, IC50 values (98.30-248.60, reducing power (0.6377-0.7702 and total antioxidant capacity (22.75-43.80 AAE/gm at different solvents and techniques. Current study data shown higher extract yields, phenolic contents, scavenging activity, reducing power and antioxidant activity using ethanol solvent compared to the respective acetone solvent. In addition, higher extract yields and other properties were obtained by hot extraction at 400C compared to the cold extraction at 260C. Present study suggests that ethanol as a solvent and hot extraction technique could be better to preserve the antioxidant properties of tamarind seed. [J Adv Vet Anim Res 2015; 2(3.000: 332-337

  2. Vanadium recovery from oil fly ash by leaching, precipitation and solvent extraction processes.

    Science.gov (United States)

    Navarro, R; Guzman, J; Saucedo, I; Revilla, J; Guibal, E

    2007-01-01

    In order to reduce the environmental impact due to land disposal of oil fly ash from power plants and to valorize this waste material, the removal of vanadium was investigated using leaching processes (acidic and alkaline treatments), followed by a second step of metal recovery from leachates involving either solvent extraction or selective precipitation. Despite a lower leaching efficiency (compared to sulfuric acid), sodium hydroxide was selected for vanadium leaching since it is more selective for vanadium (versus other transition metals). Precipitation was preferred to solvent extraction for the second step in the treatment since: (a) it is more selective; enabling complete recovery of vanadate from the leachate in the form of pure ammonium vanadate; and (b) stripping of the loaded organic phase (in the solvent extraction process) was not efficient. Precipitation was performed in a two-step procedure: (a) aluminum was first precipitated at pH 8; (b) then ammonium chloride was added at pH 5 to bring about vanadium precipitation.

  3. Effect of Ethanol/Water Solvents on Phenolic Profiles and Antioxidant Properties of Beijing Propolis Extracts

    Science.gov (United States)

    Sun, Chunli; Wu, Zhengshuang; Wang, Ziyan; Zhang, Hongcheng

    2015-01-01

    Propolis is a natural substance known to be beneficial for human health and used as a folk medicine in many parts of the world. In this study, phenolic profiles and antioxidant properties of Beijing propolis extracted by different ethanol/water solvents were analyzed. Our results reveal that phenolic compounds and antioxidant properties of propolis extracts were significantly dependent on the concentration of ethanol/water solvents. Totally, 29 phenolic compounds were identified: 12 phenolic acids, 13 flavonoids, and 4 phenolic acid esters. In particular, 75 wt.% ethanol/water solvent may be the best for the highest extraction yield and the strongest antioxidant properties. Caffeic acid, benzyl caffeate, phenethyl caffeate, 5-methoxy pinobanksin, pinobanksin, pinocembrin, pinobanksin-3-O-acetate, chrysin, and galangin were the characteristic compounds of Beijing propolis, and these compounds seem to verify that Beijing propolis may be poplar-type propolis. In addition, the presence of high level of pinobanksin-3-O-acetate in Chinese propolis may be a novel finding, representing one-third of all phenolics. PMID:26351514

  4. Coupling a Transient Solvent Extraction Module with the Separations and Safeguards Performance Model

    Energy Technology Data Exchange (ETDEWEB)

    de Almeida, Valmor F [ORNL; Birdwell Jr, Joseph F [ORNL; DePaoli, David W [ORNL; Gauld, Ian C [ORNL

    2009-10-01

    A past difficulty in safeguards design for reprocessing plants is that no code existed for analysis and evaluation of the design. A number of codes have been developed in the past, but many are dated, and no single code is able to cover all aspects of materials accountancy, process monitoring, and diversion scenario analysis. The purpose of this work was to integrate a transient solvent extraction simulation module developed at Oak Ridge National Laboratory, with the SSPM Separations and Safeguards Performance Model, developed at Sandia National Laboratory, as a first step toward creating a more versatile design and evaluation tool. The SSPM was designed for materials accountancy and process monitoring analyses, but previous versions of the code have included limited detail on the chemical processes, including chemical separations. The transient solvent extraction model is based on the ORNL SEPHIS code approach to consider solute build up in a bank of contactors in the PUREX process. Combined, these capabilities yield a much more robust transient separations and safeguards model for evaluating safeguards system design. This coupling and the initial results are presented. In addition, some observations toward further enhancement of separations and safeguards modeling based on this effort are provided, including: items to be addressed in integrating legacy codes, additional improvements needed for a fully functional solvent extraction module, and recommendations for future integration of other chemical process modules.

  5. Coupling a transient solvent extraction module with the separations and safeguards performance model.

    Energy Technology Data Exchange (ETDEWEB)

    DePaoli, David W. (Oak Ridge National Laboratory, Oak Ridge, TN); Birdwell, Joseph F. (Oak Ridge National Laboratory, Oak Ridge, TN); Gauld, Ian C. (Oak Ridge National Laboratory, Oak Ridge, TN); Cipiti, Benjamin B.; de Almeida, Valmor F. (Oak Ridge National Laboratory, Oak Ridge, TN)

    2009-10-01

    A number of codes have been developed in the past for safeguards analysis, but many are dated, and no single code is able to cover all aspects of materials accountancy, process monitoring, and diversion scenario analysis. The purpose of this work was to integrate a transient solvent extraction simulation module developed at Oak Ridge National Laboratory, with the Separations and Safeguards Performance Model (SSPM), developed at Sandia National Laboratory, as a first step toward creating a more versatile design and evaluation tool. The SSPM was designed for materials accountancy and process monitoring analyses, but previous versions of the code have included limited detail on the chemical processes, including chemical separations. The transient solvent extraction model is based on the ORNL SEPHIS code approach to consider solute build up in a bank of contactors in the PUREX process. Combined, these capabilities yield a more robust transient separations and safeguards model for evaluating safeguards system design. This coupling and initial results are presented. In addition, some observations toward further enhancement of separations and safeguards modeling based on this effort are provided, including: items to be addressed in integrating legacy codes, additional improvements needed for a fully functional solvent extraction module, and recommendations for future integration of other chemical process modules.

  6. Antimicrobial potential of Ricinus communis leaf extracts in different solvents against pathogenic bacterial and fungal strains

    Institute of Scientific and Technical Information of China (English)

    Rabia Naz; Asghari Bano

    2012-01-01

    Objective: To investigate the in vitro antimicrobial activities of the leaf extract in different solvents viz., methanol, ethanol and water extracts of the selected plant Ricinus communis. Methods:Agar well diffusion method and agar tube dilution method were carried out to perform the antibacterial and antifungal activity of methanol, ethanol and aqueous extracts. Results:Methanol leaf extracts were found to be more active against Gram positive bacteria (Bacillus subtilis: ATCC 6059 and Staphylococcus aureus: ATCC 6538) as well as Gram negative bacteria (Pseudomonas aeruginosa: ATCC 7221 and Klebsiella pneumoniae) than ethanol and aqueous leaf extracts. Antifungal activity of methanol and aqueous leaf extracts were also carried out against selected fungal strains as Aspergillus fumigatus and Aspergillus flavus. Methanolic as well as aqueous leaf extracts of Ricinus communis were effective in inhibiting the fungal growth. Conclusions: The efficient antibacterial and antifungal activity of Ricinus communis from the present investigation revealed that the methanol leaf extracts of the selected plant have significant potential to inhibit the growth of pathogenic bacterial and fungal strains than ethanol and aqueous leaf extracts.

  7. Selective separation of Cu (II), Zn (II), and Cd (II) by solvent extraction

    Institute of Scientific and Technical Information of China (English)

    XIE Keng; WEN Jiankang; HUA Yixin; RUAN Renman

    2008-01-01

    An experimental investigation was presented on the separation of Cu (II), Zn (II), and Cd (II) from a rich sulfate leachate of zinc slag by solvent extraction. The results of orthogonal experiments indicate that LIX 984N is highly selective and very efficient in the extraction of Cu (II), and the analysis of variance indicates that the sequence of parameters according to their influence on the separation efficiency is phase ratio>LIX 984N concentration>pH value>extraction time. The optimal condition for copper extraction is obtained as 25% of LIX 984N concentration, 7 min of extraction time, 3:2 of phase ratio O/A, and pH=1.7. The separation of Zn (II) and Cd (II) was performed after the copper extraction from the raffinate. Comparative analysis of the separation with di-2-ethylhexyl phosphoric acid (D2EHPA), D2EHPA-tributyl-phosophate (TBP) synergistic extracting system, and 2-ethylhexyl phosphonic acid mono 2-ethylhexyl ester (HEHEHP) was made at pH=2.0. It is demonstrated that the extraction efficiency with D2EHPA is improved after being saponified by sodium hydroxide, and D2EHPA-TBP synergistic extracting, as well as HEHEHP, has a superior selectivity to Zn (II) over Cd (II).

  8. Antimicrobial potential of Ricinus communis leaf extracts in different solvents against pathogenic bacterial and fungal strains.

    Science.gov (United States)

    Naz, Rabia; Bano, Asghari

    2012-12-01

    To investigate the in vitro antimicrobial activities of the leaf extract in different solvents viz., methanol, ethanol and water extracts of the selected plant Ricinus communis. Agar well diffusion method and agar tube dilution method were carried out to perform the antibacterial and antifungal activity of methanol, ethanol and aqueous extracts. Methanol leaf extracts were found to be more active against Gram positive bacteria (Bacillus subtilis: ATCC 6059 and Staphylococcus aureus: ATCC 6538) as well as Gram negative bacteria (Pseudomonas aeruginosa: ATCC 7221 and Klebsiella pneumoniae) than ethanol and aqueous leaf extracts. Antifungal activity of methanol and aqueous leaf extracts were also carried out against selected fungal strains as Aspergillus fumigatus and Aspergillus flavus. Methanolic as well as aqueous leaf extracts of Ricinus communis were effective in inhibiting the fungal growth. The efficient antibacterial and antifungal activity of Ricinus communis from the present investigation revealed that the methanol leaf extracts of the selected plant have significant potential to inhibit the growth of pathogenic bacterial and fungal strains than ethanol and aqueous leaf extracts.

  9. Investigation of aggregation in solvent extraction of lanthanides by acidic extractants (organo-phosphorus and naphthenic acid)

    Institute of Scientific and Technical Information of China (English)

    周乃扶; 吴瑾光; 俞致健; 王笃金; 徐光宪

    1997-01-01

    Three acidic extractants (Ⅰ) di(2-ethylhexyl) phosphoric acid (HDEHP),(Ⅱ) 2-ethylhexyl phos-phonic acid mono-2-ethylhexyl ester (KEHPEHE) and (Ⅲ) naphthenic acid were employed in preparing the samples for the characterization of the coordination structure of lanthanlde-extractant complexes and the physicochemical nature of aggregates formed in the organic diluent of the solvent extraction systems.Photo correlation spectroscopy (PCS) re-suits on the aggregates formed by the partially saponified HDEHP in n -heptane showed that the hydrodynamic radius of the aggregates was comparable to the molecular dimensions of HDEHP.The addition of 2-octanol into the diluent,by which the mixed solvent was formed,increased the dimensions of the corresponding aggregates.Aggregates formed from the ianthamde ions and HDEHP in the organic phase of the extraction systems were found very unstable.In the case of naphthenic acid,PCS data showed the formation of w/o microemulsion from the saponified naphthenic acid in the mix

  10. 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.

  11. Separation of cobalt and nickel by non-equilibrium solvent extraction

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The separation of cobalt and nickel in the ammoniacal sulfate solution by non-equilibrium solvent extraction with a phosphate (P303) as extractant was studied. In the experiment, the effects of equilibrium pH value in aqueous phase, contact time of the two phases, the air-blowing time for feed liquor in the open beaker on percentage extraction of cobalt and nickel and percentage reextraction of nickel from the loaded organic phase with dilute H2SO4. etc were studied. The results showed that: Co(Ⅱ) can be oxidized to Co(Ⅲ)-ammino-complex by adding (NH4)2S2O8 or blowing air to the aqueous phase, and Co(Ⅲ)-ammino-complex is a kind of kinetically inert complex. Its extractive speed is very slow, while the nickel′s is much faster than that of cobalt. By controlling the contact time of the two phases, nickel can be separated from cobalt by non-equilibrium solvent extraction. Then nickel was reextracted from the loaded organic phase with dilute H2SO4.

  12. Relationship between dieldrin uptake in cucumber and solvent-extractable residue in soil.

    Science.gov (United States)

    Sakai, Mizuki; Seike, Nobuyasu; Murano, Hirotatsu; Otani, Takashi

    2009-12-09

    To prevent the distribution of cucumbers with dieldrin contamination exceeding the limit set by the Japanese Food Sanitation Law, the extraction solvent for dieldrin-contaminated soil was selected prior to cultivation so that the dieldrin residue level in cucumber could be predicted. The exhaustive extraction from soil could not explain the dieldrin uptake by cucumber plants. However, significant correlation (R(2) = 0.966, P dieldrin concentrations in cucumber and dieldrin concentrations extracted with 50% (v/v) methanol-water solution from soils. This was a result of the phytoavailability of dieldrin to the cucumber plants. The extractability of soil dieldrin with the methanol-water solution decreased as the organic carbon content in the soils increased. This suggested that a 50% (v/v) methanol-water solution is the optimal solution for predicting dieldrin concentrations in cucumbers by soil analysis.

  13. Hydrolysis of fluorotelomer compounds leading to fluorotelomer alcohol production during solvent extractions of soils.

    Science.gov (United States)

    Dasu, Kavitha; Royer, Laurel A; Liu, Jinxia; Lee, Linda S

    2010-11-01

    The experimental approaches used in assessing the biodegradability of fluorotelomer-based surfactants and polymers have been under increasing scrutiny. These substances consist of an aliphatic or aromatic backbone linked to perfluoroethyl moieties by ester, ether or urethane linkages. These linkages when broken yield fluorotelomer alcohols (FTOHs), which are known to biotransform to a suite of polyfluorinated metabolites including perfluorinated carboxylic acids. Quantifying FTOH levels with minimal experimental artifacts is imperative in properly assessing the biotransformation potential and half-lives of fluorotelomer-based materials. We examined the potential for solvent-enhanced ester hydrolysis of fluorotelomer compounds with different hydrocarbon backbones including a monoester stearate (FTS), a citrate tri-ester (TBC), an acrylate (FTA), and a 2,4-toluenediamine urethane (FTU) in acetonitrile, methyl-t-butyl ether (MTBE), and ethyl acetate with live, autoclaved, 60Co-γ-irradiated, and heat-treated (400°C) soils. Substantial hydrolysis only occurred with FTS in live and γ-irradiated soils for which microbial enzymes are expected to be active, but not in autoclaved soils where enzymes are deactivated. Acetonitrile and methanol (solvents with higher dielectric constants) enhanced hydrolysis by an order of magnitude compared to less polar solvents such as MTBE and ethyl acetate. For example, in a 24-h extraction with acetonitrile of FTS-amended soil, >5wt.% FTOH was produced compared to ethyl acetate or MTBE. FTA hydrolysis was <0.7 wt.% after a 15-h extraction period and was not solvent dependent. No statistically significant solvent-enhanced hydrolysis was observed for TBC, FTA or FTU.

  14. Fast determination of bioactive phytic acid and pyrophosphate in walnuts using microwave accelerated extraction.

    Science.gov (United States)

    Liu, Tong; He, Liu; Valiente, Manuel; López-Mesas, Montserrat

    2017-04-15

    Bioactive compounds phytic acid (IP6) and pyrophosphate (PPi) are minor components of walnuts with the ability of being inhibitors of urolithiasis, among others. Since simultaneous analysis of IP6 and PPi have known drawbacks, a new method to determine their content in walnuts has been developed with emphasis on their extraction from walnuts by microwave-assisted extraction (MAE). Acid content of extracting solvent, extraction time and temperature were optimized. After extraction, compounds were purified by selective adsorption/desorption on an anion exchange solid phase extraction and analyzed by inductive coupled plasma/mass spectrometry. A mixture of H2SO4 and HCl as solvent to extract both, IP6 and PPi, provided results slightly higher than those determined by conventional extraction with no statistical difference. The possible hydrolysis of phytic acid by MAE was analyzed. Compared with the conventional acid extraction method, significant improvement is achieved by the MAE method reducing extraction time from 3h to 10min.

  15. Chemical profiling of Curcuma aeruginosa Roxb. rhizome using different techniques of solvent extraction

    Institute of Scientific and Technical Information of China (English)

    Sanimah; Simoh; Alizah; Zainal

    2015-01-01

    Objective:To investigate the possible phytochemical constituents of Curcuma aeruginosa Roxb.(C. aeruginosa) rhizome using two different techniques of direct solvent extraction. Methods: Two different techniques of direct solvent extractions, i.e. methyl tert-butyl ether(MTBE) extraction and two-phase methanol/chloroform(M/C) system, were used in this study. The analysis of the phytochemical constituents in MTBE and M/C extracts was performed using gas chromatography-mass spectrometry/mass spectrometry. The mass spectra of the compounds was matched with the NIST 08 mass spectral library. Results: The present study revealed that the extraction using two-phase M/C have resulted in higher metabolite coverage compared to the extraction with MTBE. Direct solvent extraction using MTBE revealed the presence of 27 compounds; whereas, M/C allowed the extraction of 18 and 36 compounds in polar(methanol) and nonpolar(chloroform) fractions respectively. The major compounds detected in the MTBE extract that based on the peak area percentage were methenolone(16.64%), cycloisolongifolene, 8,9-dehydro-9-formyl-(15.93%), labd-13-en-15-oic acid,8,12-epoxy-12-hydroxy-γ-lactone(10.77%), propiolic acid, 3-(1-hydroxy)-2 isopropyl-1,5-methylcyclohexyl)(7.84%), 4-oxo-β-isodamascol(5.17%), velleral(3.11%) and Z-α-farnesene(2.00%). The most prevailing major compounds identified in the polar fraction of the M/C extraction were α-D glucopyranoside, 1,3,4,6 tetrakis-O-(TMS)(trimethylsilyl)-β-D-fructofuranosyl 2,3,4,6-tetrakis-O-(TMS)-(38.08%), d-glucose, 2,3,4,5,6-pentakis-O-(TMS)-, O-methyloxime(14.61%), D-fructose, 1,3,4,5,6-pentakis-O-(TMS)-, O-methyloxime(5.28%), isocitric acid(TMS)(3.06%), oxalic acid, bis(TMS) ester(2.96%), hexadecanoic acid, TMS ester(2.16%), citric acid, ethyl ester, tri-TMS(1.91%) and butanedioic acid, [(TMS) oxy]-, bis(TMS) ester(1.14%); whereas in the nonpolar extract, among the major compounds detected were cycloisolongifolene, 8, 9-dehydro-9-formyl(15

  16. Application of 2k Full Factorial Design in Optimization of Solvent-Free Microwave Extraction of Ginger Essential Oil

    Directory of Open Access Journals (Sweden)

    Mumtaj Shah

    2014-01-01

    Full Text Available The solvent-free microwave extraction of essential oil from ginger was optimized using a 23 full factorial design in terms of oil yield to determine the optimum extraction conditions. Sixteen experiments were carried out with three varying parameters, extraction time, microwave power, and type of sample for two levels of each. A first order regression equation best fits the experimental data. The predicted values calculated by the regression model were in good agreement with the experimental values. The results showed that the extraction time is the most prominent factor followed by microwave power level and sample type for extraction process. An average of 0.25% of ginger oil can be extracted using current setup. The optimum conditions for the ginger oil extraction using SFME were the extraction time 30 minutes, microwave power level 640 watts, and sample type, crushed sample. Solvent-free microwave extraction proves a green and promising technique for essential oil extraction.

  17. Instrument for Solvent Extraction and Analysis (ISEE) of Organics from Regolith Simulant Using Supercritical Fluid Extraction and Chromatography

    Science.gov (United States)

    Franco, Carolina; Hintze, Paul E.

    2017-01-01

    ISEE is an instrument with the potential to perform extractions from regolith found on the surface of asteroids and planets, followed by characterization and quantitation of the extracts using supercritical fluid extraction (SFE) and chromatography (SFC). SFE is a developed technique proven to extract a wide range of organic compounds. SFC is similar to High Performance Liquid Chromatography (HPLC) but has the advantage of performing chiral separations without needing to derivatize the chiral compounds. CO2 will be the solvent for both stages as it is readily available in the Mars atmosphere. ISEE will capture CO2 from the environment, and use it for SFE and SFC. If successful, this would allow ISEE to perform analysis of organic compounds without using consumables. This paper will present results on a preliminary, proof-of-principle effort to use SFE and SFC to extract and analyze lunar regolith simulant spiked with organic compounds representing a range of organics that ISEE would expect to characterize. An optimization of variables for the extraction of the organics from the spiked regolith was successfully developed, using 138 bar pressure and 40 C temperature. The extraction flow rate was optimized at 2% SLPM with 30% methanol modifier. The extractions were successful with a value of 77.3+/- 0.9% of organics extracted. However, the recovery of organics after the extraction was very low with only 48.5+/-14.2%. Moreover, three columns were selected to analyze multiple samples at a time; two of them are Viridis HSS C18 SB and Torus DIOL, and the third column, specific for chiral separations, has not yet been selected yet.

  18. Study on the 3-hydroxy-3-methyl-glutaryl CoA reductase inhibitory properties of Agaricus bisporus and extraction of bioactive fractions using pressurised solvent technologies.

    Science.gov (United States)

    Gil-Ramírez, Alicia; Clavijo, Cristina; Palanisamy, Marimuthu; Ruiz-Rodríguez, Alejandro; Navarro-Rubio, María; Pérez, Margarita; Marín, Francisco R; Reglero, Guillermo; Soler-Rivas, Cristina

    2013-08-30

    Agaricus bisporus mushrooms were able to lower cholesterol levels in hypercholesterolaemic rats and it was suggested that dietary fibre might inhibit cholesterol absorption. However, A. bisporus extracts were also able to inhibit the 3-hydroxy-3-methyl-glutaryl CoA reductase (HMGCR, the key enzyme in the cholesterol biosynthetic pathway) and this might also contribute to the observed lowering of cholesterol levels in serum. The methanol-water extracts obtained from A. bisporus were able to inhibit up to 60% the HMGCR activity using an in vitro assay. The HMGCR inhibitory capacities depended on cultivation conditions, strains, etc. The potential inhibitors were not statins, they might be β-glucans able to scavenge the substrate and impair the enzymatic reaction. They were present during all mushroom developmental stages and similarly distributed through all the tissues including the parts discarded as a by-product. Accelerated solvent extractions using 1:1 ethanol-water as pressurised solvent (10.7 MPa, 25°C, five cycles of 5 min) were more effective in the extraction of the HMGCiR inhibitor(s) than supercritical fluid extractions (9 MPa, 40°C) using CO2 with 10% ethanol. A mushroom cultivation and two extraction procedures were optimised to obtain fractions from A. bisporus with high HMGCR inhibitory activities to design novel ingredients for hypocholesterolaemic functional foodstuffs. © 2013 Society of Chemical Industry.

  19. Ethanol as a solvent and hot extraction technique preserved the antioxidant properties of tamarind (Tamarindus indica) seed

    OpenAIRE

    Nushrat Yeasmen; Md. Nazrul Islam

    2015-01-01

    The influence of two extraction solvents (ethanol and acetone) and two extraction techniques i.e., hot extraction at 400C and cold extraction at 260C were investigated on the phenolic content and antioxidant activity of extracts from Tamarindus indica seed. The antioxidant activity of T. indica was determined by evaluating 1,1-Diphenyl-2-picrylhydrazyl (DPPH) scavenging activity, ferric reducing power assay (FRAP) and ascorbic acid equivalent content (AAC). The tested sample showed appreciabl...

  20. Solvent effects on extraction of polycyclic aromatic hydrocarbons in ambient aerosol samples

    Directory of Open Access Journals (Sweden)

    Flasch Mira

    2016-01-01

    Full Text Available Polycyclic Aromatic Hydrocarbons (PAHs in the ambient particulate matter pose one of the most important issues in the focus of environmental management. The concentration of their representative, Benzo(apyrene (BaP, undergoes limitations according to European Union directive. However, a successful control over the pollution levels and their sources is limited by the high uncertainty of analytical and statistical approaches used for their characterization. Here we compare differences in PAH concentrations related to the use of different solvents in the course of ultrasonic extraction of a certified reference material (PM10-like PAH mixture and filter samples of ambient particulate matter collected in Austria for the CG-MS PAH analysis. Using solvents of increasing polarity: Cyclohexane (0,006, Toluene (0,099, Dichloromethane (0,309, Acetone (0,43 and Acetonitrile (0,460, as well as mixtures of those, filters representing high and low concentrations of particulate matter were investigated. Although some scatter of the obtained concentrations was observed no trend related to the polarity of the solvent became visible. Regarding the reproducibility, which can be expected of PAH analysis no significant difference between the different solvents was determined. This result is valid for all compounds under investigation.

  1. Alternative Bio-Based Solvents for Extraction of Fat and Oils: Solubility Prediction, Global Yield, Extraction Kinetics, Chemical Composition and Cost of Manufacturing

    Directory of Open Access Journals (Sweden)

    Anne-Gaëlle Sicaire

    2015-04-01

    Full Text Available The present study was designed to evaluate the performance of alternative bio-based solvents, more especially 2-methyltetrahydrofuran, obtained from crop’s byproducts for the substitution of petroleum solvents such as hexane in the extraction of fat and oils for food (edible oil and non-food (bio fuel applications. First a solvent selection as well as an evaluation of the performance was made with Hansen Solubility Parameters and the COnductor-like Screening MOdel for Realistic Solvation (COSMO-RS simulations. Experiments were performed on rapeseed oil extraction at laboratory and pilot plant scale for the determination of lipid yields, extraction kinetics, diffusion modeling, and complete lipid composition in term of fatty acids and micronutrients (sterols, tocopherols and tocotrienols. Finally, economic and energetic evaluations of the process were conducted to estimate the cost of manufacturing using 2-methyltetrahydrofuran (MeTHF as alternative solvent compared to hexane as petroleum solvent.

  2. Alternative bio-based solvents for extraction of fat and oils: solubility prediction, global yield, extraction kinetics, chemical composition and cost of manufacturing.

    Science.gov (United States)

    Sicaire, Anne-Gaëlle; Vian, Maryline; Fine, Frédéric; Joffre, Florent; Carré, Patrick; Tostain, Sylvain; Chemat, Farid

    2015-04-15

    The present study was designed to evaluate the performance of alternative bio-based solvents, more especially 2-methyltetrahydrofuran, obtained from crop's byproducts for the substitution of petroleum solvents such as hexane in the extraction of fat and oils for food (edible oil) and non-food (bio fuel) applications. First a solvent selection as well as an evaluation of the performance was made with Hansen Solubility Parameters and the COnductor-like Screening MOdel for Realistic Solvation (COSMO-RS) simulations. Experiments were performed on rapeseed oil extraction at laboratory and pilot plant scale for the determination of lipid yields, extraction kinetics, diffusion modeling, and complete lipid composition in term of fatty acids and micronutrients (sterols, tocopherols and tocotrienols). Finally, economic and energetic evaluations of the process were conducted to estimate the cost of manufacturing using 2-methyltetrahydrofuran (MeTHF) as alternative solvent compared to hexane as petroleum solvent.

  3. Sequential extraction of flavonoids and pectin from yellow passion fruit rind using pressurized solvent or ultrasound.

    Science.gov (United States)

    de Souza, Caroline G; Rodrigues, Tigressa Hs; E Silva, Lorena Ma; Ribeiro, Paulo Rv; de Brito, Edy S

    2017-07-31

    Passion fruit rind (PFR) represents 90% of the total fruit weight and is wasted during juice processing. Passion fruit rind is known to contain flavonoids and pectin. An alternative use for this fruit juice industrial residue is to obtain these compounds. This study aimed to verify the influence of pressurized solvent extraction (PSE) or ultrasound assisted extraction (UAE) of flavonoid and pectin in a sequential process. The PSE using ethanol at 60:40 (v/v) yielded a total polyphenol content of 4.67 g GAE kg(-1) PFR, orientin-7-O-glucoside (1.57 g kg(-1) PFR) and luteolin-6-C-glucoside (2.44 g kg(-1) PFR). Pectin yield was 165 g kg(-1) PFR, either in PSE or UAE. Pectin characterization indicates that the pectic structure has basically homogalacturonans and galacturonate followed by a galacturonic acid ester unit, with methylation degree of 70%. With this study it can be concluded that mixtures of alcohols with water favor the extraction of bioactive compounds of passion fruit peel. Both PSE and UAE were effective in sequentially extracting flavonoids and pectin. The preferred solvent is ethanol due to its lower toxicity. © 2017 Society of Chemical Industry. © 2017 Society of Chemical Industry.

  4. A solvent extraction technique for the isotopic measurement of dissolved copper in seawater

    Energy Technology Data Exchange (ETDEWEB)

    Thompson, Claire M., E-mail: claire.thompson@anu.edu.au; Ellwood, Michael J., E-mail: michael.ellwood@anu.edu.au; Wille, Martin, E-mail: martin.wille@uni-tuebingen.de

    2013-05-02

    Graphical abstract: -- Highlights: •A new sample preparation method for seawater copper isotopic analysis (δ{sup 65}Cu). •Solvent-extraction was used to pre-concentrate metals from seawater samples. •Anion-exchange was used to purify copper from the metal-rich extract. •δ{sup 65}Cu was measured in the north Tasman Sea. •Seawater δ{sup 65}Cu may be linked to marine biological activity. -- Abstract: Stable copper (Cu) isotope geochemistry provides a new perspective for investigating and understanding Cu speciation and biogeochemical Cu cycling in seawater. In this work, sample preparation for isotopic analysis employed solvent-extraction with amino pyrollidine dithiocarbamate/diethyl dithiocarbamate (APDC/DDC), coupled with a nitric acid back-extraction, to concentrate Cu from seawater. This was followed by Cu-purification using anion-exchange. This straightforward technique is high yielding and fractionation free for Cu and allows precise measurement of the seawater Cu isotopic composition using multi-collector inductively coupled plasma mass-spectrometry. A deep-sea profile measured in the oligotrophic north Tasman Sea shows fractionation in the Cu isotopic signature in the photic zone but is relatively homogenised at depth. A minima in the Cu isotopic profile correlates with the chlorophyll a maximum at the site. These results indicate that a range of processes are likely to fractionate stable Cu isotopes in seawater.

  5. Extraction of Bioactive Compounds as Natural Antioxidants from Fresh Spirulina platensis using Different Solvents

    Directory of Open Access Journals (Sweden)

    Fiya Firdiyani

    2015-06-01

    Full Text Available Spirulina platensis is a bioactive-rich microalga of great potential as a source of natural antioxidant. Natural antioxidants are increasing in demand, because it is considered as more safe than synthetic antioxidants. The objective of this study was to determine the effect of solvent on the potential of natural antioxidant from fresh S. platensis. The antioxidant compound was extracted using either acetone or ethyl acetate by reflux method. The yield of extractions were 1.86% and 3.07% for aceton and ethyl acetate, respectively. Fresh S. platensis extracts were considered as potential antioxidant source with IC50 values 65.89 ppm, and 76.36 ppm when using acetone and ethyl acetate, respectivetly, even though it were still lower compare to the IC50 of positive control quercetin i.e 21.64 ppm. Phytochemical test showed positive results of phenolic compound, triterpenoids, steroid, flavanoid, and saponin. aw value of Spirulina platensis was 0.61 and 0.81 for aceton and ethyl acetate, respectively. It was concluded that different solvent affected the antioxidant activity of S. platensis extract. Keywords: Antioxidants, aceton, ethyl acetate, fresh Spirulina platensis

  6. Extraction of Bioactive Compounds as Natural Antioxidants from Fresh Spirulina platensis using Different Solvents

    Directory of Open Access Journals (Sweden)

    Fiya Firdayani

    2015-06-01

    Full Text Available Spirulina platensis is a bioactive-rich microalga of great potential as a source of natural antioxidant. Natural antioxidants are increasing in demand, because it is considered as more safe than synthetic antioxidants. The objective of this study was to determine the effect of solvent on the potential of natural antioxidant from fresh S. platensis. The antioxidant compound was extracted using either acetone or ethyl acetate by reflux method. The yield of extractions were 1.86% and 3.07% for aceton and ethyl acetate, respectively. Fresh S. platensis extracts were considered as potential antioxidant source with IC50 values 65.89 ppm, and 76.36 ppm when using acetone and ethyl acetate, respectivetly, even though it were still lower compare to the IC50 of positive control quercetin i.e 21.64 ppm. Phytochemical test showed positive results of phenolic compound, triterpenoids, steroid, flavanoid, and saponin. aw value of Spirulina platensis was 0.61 and 0.81 for aceton and ethyl acetate, respectively. It was concluded that different solvent affected the antioxidant activity of S. platensis extract.

  7. Pyrolysates of raw vitrinites and their residues after CS2-NMP solvent extraction and its significance for petroleum geology

    Institute of Scientific and Technical Information of China (English)

    LIU Dayong; PENG Ping'an

    2006-01-01

    Binary solvent (CS2-NMP) has extreme high extraction ability to coals, and it can extract most bitumens out of coals and vitrinites. And large amount of messages on side chains and their distribution character in vitrinites should be acquired through flash pyrolysis before and after binary solvent (CS2-NMP) extraction. A few low maturated coals have been selected and vitrinites are handpicked from coals. Then vitrinites have been extracted using different solvents in the order of polarity. Flash pyrolysis-Gas Chromatography/Mass spectrum has been applied to samples. The result shows that CS2-NMP is efficient for the extraction of vitirnites, giving much higher extraction yield than common solvents. Production ratio of liquid hydrocarbons in pyrolysates of vitrinites extracted with CS2-NMP is lower than that of raw vitrinites. And relative ratio of each component in pyrolysates has changed apparently. Production ratio of aliphatic hydrocarbons, especially those long chain aliphatics have decreased much after mixed solvent extraction. It shows that bitumens extracted with CS2-NMP have largely contributed to pyrolysates, especially those aliphatics in pyrolysates.

  8. Separation of ethanol and water by extractive distillation with salt and solvent as entrainer: process simulation

    Directory of Open Access Journals (Sweden)

    I. D. Gil

    2008-03-01

    Full Text Available The aim of this work is to simulate and analyze an extractive distillation process for azeotropic ethanol dehydration with ethylene glycol and calcium chloride mixture as entrainer. The work was developed with Aspen Plus® simulator version 11.1. Calculation of the activity coefficients employed to describe vapor liquid equilibrium of ethanol - water - ethylene glycol - calcium chloride system was done with the NRTL-E equation and they were validated with experimental data. The dehydration process used two columns: the main extractive column and the recovery column. The solvent to feed molar ratio S/F=0.3, molar reflux ratio RR=0.35, number of theoretical stages Ns=18, feed stage Sf=12, feed solvent stage SS=3, and feed solvent temperature TS=80 ºC, were determined to obtain a distillate with at least 99.5 % mole of ethanol. A substantial reduction in the energy consumption, compared with the conventional processes, was predicted by using ethylene glycol and calcium chloride as entrainer.

  9. Treatment of phenol in synthetic saline wastewater by solvent extraction and two-phase membrane biodegradation.

    Science.gov (United States)

    Juang, Ruey-Shin; Huang, Wen-Ching; Hsu, Ya-Han

    2009-05-15

    Phenol in synthetic saline (100gL(-1) NaCl) and acidic (pH 3) wastewater was treated by a hybrid solvent extraction and two-phase membrane biodegradation process at 30 degrees C. Kerosene was adopted to be the organic solvent because it was biocompatible and had a suitable partition coefficient for phenol. Phenol in water was first extracted by kerosene in a batch stirred vessel and the loaded solvent was passed through the lumen of a polyvinylidene fluoride (PVDF) hollow-fiber membrane contactor; in the meantime, Pseudomonas putida BCRC 14365 in mineral salt medium was flowed across the shell, to which tetrasodium phyophosphate (1gL(-1)) was added as a dispersing agent. The effect of the initial phenol level in wastewater (110-2400mgL(-1)) on phenol removal and cell growth was experimentally studied. At a cell concentration of 0.023gL(-1), it was shown that the removal of phenol from saline wastewater was more efficient at a level of 2000mgL(-1) when 0.02-m(2) membrane module was used. The effects of bigger membrane module size (0.19m(2) area) and higher initial cell concentration (0.092-0.23gL(-1)) on the performance of such a hybrid process for the treatment of higher-level phenol in saline wastewater was also evaluated and discussed.

  10. Solvent-extraction methods applied to the chemical analysis of uranium. III. Study of the extraction with inert solvents; Metodos de extraccion con disolventes aplicados al analisis quimico del uranio. III. Estudio de la extraccion con disolvente inertes

    Energy Technology Data Exchange (ETDEWEB)

    Vera Palomino, J.; Palomares Delgado, F.; Petrement Eguiluz, J. C.

    1964-07-01

    The extraction of uranium on the trace level is studied by using tributylphosphate as active agent under conditions aiming the attainment of quantitative extraction by means of a single step process using a number of salting-out agents and keeping inside the general lines as reported in two precedent papers. Two inert solvents were investigated, benzene and cyclohexane, which allowed to derive the corresponding empirical equations describing the extraction process and the results obtained were compared with those previously reported for solvents which, like ethyl acetate and methylisobuthylketone, favour to a more or less extend the extraction of uranium. (Author) 4 refs.

  11. Determination of selected polychlorinated biphenyls in soil by miniaturised ultrasonic solvent extraction and gas chromatography-mass-selective detection.

    Science.gov (United States)

    Aydin, Mehmet Emin; Tor, Ali; Ozcan, Senar

    2006-09-08

    Miniaturised ultrasonic solvent extraction procedure was developed for the determination of selected polychlorinated biphenyls (PCBs) in soil samples by gas chromatography-mass-selective detection by using 2(3) factorial experimental design. Recoveries of PCBs from fortified soil samples are over 90% for three different fortification levels between 40 and 120 microg kg(-1), and relative standard deviations of the recoveries are below 7%. The limits of detection (LODs) ranged from 0.003 to 0.006 microg kg(-1). The performance of the proposed method was compared to traditional shake flask extraction method on the spiked real soil sample and extraction methods showed comparable efficiencies. Proposed miniaturised ultrasonic solvent extraction offers several advantages, i.e., reducing sample requirement for measurement of target compound, less solvent consumption and reducing the costs associated with solvent purchase and waste disposal.

  12. Correlation between aggregation and extracting properties in solvent extraction systems: extraction of actinides (III) and lanthanides (III) by a malonamide in non acidic media

    Energy Technology Data Exchange (ETDEWEB)

    Meridiano, Y.; Berthon, L.; Lagrave, S.; Crozes, X.; Sorel, C.; Testard, F.; Zemb, T. [CEA Marcoule, DEN/DRCP/SCPS/LCSE, 30207Bagnols sur Ceze (France)

    2008-07-01

    The organic phases of the DIAMEX (Diamide Extraction) process, allowing the co-extraction of actinides(III) and lanthanides(III) from high level radioactive wastes using a malonamide extractant molecule (DMDOHEMA) diluted in alkanes, are investigated. The aim of this study is to establish a link between different structures/organizations of diamide extractants and their extracting properties towards An(III) and Ln(III) cations. It is demonstrated that diamide, which are amphiphilic molecules, are organized in different structures (monomers, reverse micelles, lamellar phases..). This study deals with the effect of the composition of the extracting system on the extracting and aggregation properties of the DMDOHEMA solutions. The effects of the extractant (DMDOHEMA diluted in n-heptane) and metal concentrations (for a given extractant concentration) from a LiNO{sub 3} aqueous phase are investigated at two scales: at the supra-molecular scale by characterizing the aggregation by vapor-pressure osmometry (VPO) and small angle neutron and X-ray scattering (SANS and SAXS) experiments, and at the molecular scale by quantifying the extracted solutes (metal nitrate and water) and by determining the stoichiometries of the extracted complexes by electro-spray mass spectrometry (ESI-MS). The extraction equilibria can then be modeled by two approaches: a classical approach in solvent extraction based on mass action laws to determine extraction equilibria and their associated thermodynamic constants, and a physical chemical approach which consists in considering the extracted ions as adsorbed on a specific available surface of the extractant molecule. Thus, the extraction equilibrium can be considered as a sum of Langmuir isotherms corresponding to the different states of aggregation. The resulting constants are representative of both extraction efficiency and organic phase structure. (authors)

  13. Solvent extraction of organic acids from stillage for its re-use in ethanol production process.

    Science.gov (United States)

    Castro, G A; Caicedo, L A; Alméciga-Díaz, C J; Sanchez, O F

    2010-06-01

    Stillage re-use in the fermentation stage in ethanol production is a technique used for the reduction of water and fermentation nutrients consumption. However, the inhibitory effect on yeast growth of the by-products and feed components that remains in stillage increases with re-use and reduces the number of possible recycles. Several methods such as ultrafiltration, electrodialysis and advanced oxidation processes have been used in stillage treatment prior its re-use in the fermentation stage. Nevertheless, few studies evaluating the effect of solvent extraction as a stillage treatment option have been performed. In this work, the inhibitory effect of serial stillage recycling over ethanol and biomass production was determined, using acetic acid as a monitoring compound during the fermentation and solvent extraction process. Raw palm oil methyl ester showed the highest acetic acid extraction from the aqueous phase, presenting a distribution coefficient of 3.10 for a 1:1 aqueous phase mixture:solvent ratio. Re-using stillage without treatment allowed up to three recycles with an ethanol production of 53.7 +/- 2.0 g L(-1), which was reduced 25% in the fifth recycle. Alternatively, treated stillage allowed up to five recycles with an ethanol final concentration of 54.7 +/- 1.3 g L(- 1). These results show that reduction of acetic acid concentration by an extraction process with raw palm oil methyl ester before re-using stillage improves the number of recycles without a major effect on ethanol production. The proposed process generates a palm oil methyl ester that contains organic acids, among other by-products, that could be used for product recovery and as an alternative fuel.

  14. DEVELOPMENT OF CONTINUOUS SOLVENT EXTRACTION PROCESSES FOR COAL DERIVED CARBON PRODUCTS

    Energy Technology Data Exchange (ETDEWEB)

    Dady B. Dadyburjor; Mark E. Heavner; Manoj Katakdaunde; Liviu Magean; J. Joshua Maybury; Alfred H. Stiller; Joseph M. Stoffa; John W. Zondlo

    2006-08-01

    The purpose of this DOE-funded effort is to develop continuous processes for solvent extraction of coal for the production of carbon products. The largest applications are those which support metals smelting, such as anodes for aluminum smelting and electrodes for arc furnaces. Other carbon products include materials used in creating fuels for the Direct Carbon Fuel Cell, and porous carbon structural material referred to as ''carbon foam'' and carbon fibers. During this reporting period, hydrotreatment of solvent was completed in preparation for pitch fabrication for graphite electrodes. Coal digestion has lagged but is expected to be complete by next quarter. Studies are reported on coal dissolution, pitch production, foam synthesis using physical blowing agents, and alternate coking techniques.

  15. Towards an understanding of solvent extraction--electroanalytical characterization of chloride-leaching solutions.

    Science.gov (United States)

    Paiva, A P; Abrantes, L M

    2001-08-01

    Solvent extraction has been employed to purify media simulating chloride-leaching solutions resulting from complex sulfide concentrate processing, and cyclic voltammetry (CV) has been chosen to characterize those hydrometallurgical aqueous phases. The possibilities of the CV technique were investigated by the evaluation of the adequacy of a specific organic extractant, triisobutylphosphine sulfide, aimed to efficiently and selectively extract silver from a complex chloride medium, additionally containing tenfold to 40-fold molar concentrations of iron, copper and lead. The influence of the oxidation state of the metallic ions present in the feed solution, namely Cu(II) and Cu(I), is considered. The possibilities of CV analysis for the characterization of stripping solutions are also illustrated.

  16. Solvent Extraction: Structure of the Liquid-Liquid Interface Containing a Diamide Ligand.

    Science.gov (United States)

    Scoppola, Ernesto; Watkins, Erik B; Campbell, Richard A; Konovalov, Oleg; Girard, Luc; Dufrêche, Jean-Francois; Ferru, Geoffroy; Fragneto, Giovanna; Diat, Olivier

    2016-08-01

    Knowledge of the (supra)molecular structure of an interface that contains amphiphilic ligand molecules is necessary for a full understanding of ion transfer during solvent extraction. Even if molecular dynamics already yield some insight in the molecular configurations in solution, hardly any experimental data giving access to distributions of both extractant molecules and ions at the liquid-liquid interface exist. Here, the combined application of X-ray and neutron reflectivity measurements represents a key milestone in the deduction of the interfacial structure and potential with respect to two different lipophilic ligands. Indeed, we show for the first time that hard trivalent cations can be repelled or attracted by the extractant-enriched interface according to the nature of the ligand.

  17. Effect of solvent addition sequence on lycopene extraction efficiency from membrane neutralized caustic peeled tomato waste.

    Science.gov (United States)

    Phinney, David M; Frelka, John C; Cooperstone, Jessica L; Schwartz, Steven J; Heldman, Dennis R

    2017-01-15

    Lycopene is a high value nutraceutical and its isolation from waste streams is often desirable to maximize profits. This research investigated solvent addition order and composition on lycopene extraction efficiency from a commercial tomato waste stream (pH 12.5, solids ∼5%) that was neutralized using membrane filtration. Constant volume dilution (CVD) was used to desalinate the caustic salt to neutralize the waste. Acetone, ethanol and hexane were used as direct or blended additions. Extraction efficiency was defined as the amount of lycopene extracted divided by the total lycopene in the sample. The CVD operation reduced the active alkali of the waste from 0.66 to lycopene efficiently from tomato processing byproducts.

  18. Separation and Recovery of Precious Metals from Leach Liquors of Spent Electronic Wastes by Solvent Extraction

    Energy Technology Data Exchange (ETDEWEB)

    Nguyen, Thi Hong; Wang, Lingyun; Lee, Man Seung [Mokpo National University, Mokpo (Korea, Republic of)

    2017-04-15

    Solvent extraction was employed to recover precious metals (Au (III), Pd (II) and Pt (IV)) from the leach solution of spent electronic wastes containing Cu (II), Cr (III) and Fe (III). First, pure Fe (III) and Au (III) were recovered by simultaneous extraction with Cyanex 923 followed by selective stripping with HCl and Na{sub 2}S{sub 2}O{sub 3}. Second, Pt (IV), Pd (II) and Cu (II) were extracted by Alamine 336 from the raffinate. After the removal of Cu (II) by stripping with weak HCl, Pd (II) and Pt (IV) were separately stripped by controlling the concentration of thiourea in the mixture with HCl. A process flow sheet for the separation of precious metals was proposed.

  19. Solvent Extraction: Structure of the Liquid-Liquid Interface Containing a Diamide Ligand

    Energy Technology Data Exchange (ETDEWEB)

    Scoppola, Ernesto [Institut Laue-Langevin, 38000 Grenoble France; Institut de Chimie Séparative de Marcoule, UMR 5257 CEA/CNRS/ENSCM/Université Montpellier, 30207 Bagnols-sur-Cèze France; Watkins, Erik B. [Institut Laue-Langevin, 38000 Grenoble France; Materials Synthesis and Integrated Devices, Los Alamos National Laboratory, Los Alamos NM 87545 USA; Campbell, Richard A. [Institut Laue-Langevin, 38000 Grenoble France; Konovalov, Oleg [European Synchrotron Radiation Facility, 38430 Grenoble France; Girard, Luc [Institut de Chimie Séparative de Marcoule, UMR 5257 CEA/CNRS/ENSCM/Université Montpellier, 30207 Bagnols-sur-Cèze France; Dufrêche, Jean-Francois [Institut de Chimie Séparative de Marcoule, UMR 5257 CEA/CNRS/ENSCM/Université Montpellier, 30207 Bagnols-sur-Cèze France; Ferru, Geoffroy [Argonne National Labororatory, Lemont IL 60439 USA; Fragneto, Giovanna [Institut Laue-Langevin, 38000 Grenoble France; Diat, Olivier [Institut de Chimie Séparative de Marcoule, UMR 5257 CEA/CNRS/ENSCM/Université Montpellier, 30207 Bagnols-sur-Cèze France

    2016-06-20

    Knowledge of the (supra)molecular structure of an interface that contains amphiphilic ligand molecules is necessary for a full understanding of ion transfer during solvent extraction. Even if molecular dynamics already yield some insight in the molecular configurations in solution, hardly any experimental data giving access to distributions of both extractant molecules and ions at the liquid–liquid interface exist. Here, the combined application of X-ray and neutron reflectivity measurements represents a key milestone in the deduction of the interfacial structure and potential with respect to two different lipophilic ligands. Indeed, we show for the first time that hard trivalent cations can be repelled or attracted by the extractant-enriched interface according to the nature of the ligand.

  20. EXTRACTION OF MALIC ACID WITH ALIQUAT-336 IN EXISTENCE OF DILUENT SOLVENTS

    Directory of Open Access Journals (Sweden)

    Mehmet BİLGİN

    2001-03-01

    Full Text Available In this study, the effect of diluents in different structures on the extraction of malic acid from aqueous solutions with Aliquat-336, named chemically as tricapril metyl ammonium chloride, was investigated. Diluting solvents used in experiments are heptane, toluene, kerosene, cyclohexane and methyl isobuthyl ketone (MIBK. Furthermore, the effect of MIBK+Heptan mixture in 1:1 volume ratio on the extraction was investigated also. The extraction was performed at room temperature by means of a shaker. The distribution coefficients and loading factors were calculated from the experimentally determined results, presented as tables and graphics, and compared with each other. Among the diluents used in this study, the best results were obtained with MIBK.

  1. Separation of flavonoids by means of solvent extraction; Yobai chushutsuho ni yoru flavonoid rui no bunri

    Energy Technology Data Exchange (ETDEWEB)

    Kitazaki, H.; Ishimaru, M. [Tsumura and Co., Tokyo (Japan); Inoue, K.; Nakamura, S. [Saga University, Saga (Japan). Faculty of Science and Engineering

    1997-03-10

    Some herb medicines may contain various flavonoids. The bioactivity of them has been attracted attention. In this paper, the separating purification method by solvent extraction was investigated. The extractant is di (ethylhexyl) amine, tributyl phosphate, N,N-dioctyl hexanamide, trioctylphosphine oxide (TOPO), and Cyanex 925. Flavonoids are considered to be separated based on the difference of solubility in an ethanol solution, the existence of a glycoside in flavonoids, and the number of hydroxyl groups or their bonding position. For example, flavone, flavonol, 7,8-dihydroxyflavone, baicalein, and baicalin are used as the representative substance of flavonoids. If a target substance is baicalin, this mixture is dissolved in an ethanol solution to eliminate insoluble matter such as flavonol. Next, flavone is extracted and eliminated by hexane. In the last step, the target baicalin is left in raffinate by TOPO or Cyanex 925. 3 refs., 7 figs., 1 tab.

  2. A solvent extraction study of molybdenum chloride and molybdenum thiocyanate complexes

    Science.gov (United States)

    Greenland, L.P.; Lillie, E.G.

    1974-01-01

    The effect of reducing agents on molybdenum(VI) solutions in hydrochloric acid was studied by a solvent extraction technique to elucidate the composition of the colored molybdenum thiocyanate complex. Neither copper(I) chloride nor ascorbic acid have any effect on the extraction of MoO2Cl2; it is inferred that tin(II) chloride reduces Mo(VI) stepwise to a polynuclear Mo(V)??Mo(VI) complex and then to Mo(V). The colored thiocyanate complex produced by copper(I) and by ascorbic acid differs only slightly in extraction characteristics from the uncolored Mo(VI) complex. It is suggested that the color may be produced by an isomerization reaction of MoO2(SCN)2, and thus that the colored species may be a hexavalent rather than pentavalent molybdenum complex. ?? 1974.

  3. Antioxidant components and properties of dry heat treated clove in different extraction solvents.

    Science.gov (United States)

    Nikousaleh, Azadeh; Prakash, Jamuna

    2016-04-01

    The effects of heat treatment and extraction solvents (pure/aqueous acetone, ethanol, methanol) on antioxidant activity (AA) and components of clove (Syzygium aromaticum Linn) were studied. Clove was subjected to dry heat treatment (microwave and roasting) and the AA measured by free radical scavenging activity (FRSA), reducing power (RP), and phospho-molybdenum assay (TAA). Unheated samples served as controls. The antioxidant components estimated were total phenols, flavonoids and tannins. Using RP and FRSA, highest AA was observed in 80 % acetone extract of all samples (1.778-1448 and 84.5-86.0 %). TAA showed higher value in 80 % methanolic extract for all samples in the range 303.595-307.941 mmol ascorbic acid/g. Heated samples exhibited higher AA in all assays. Highest amount of phenols and flavonoids were extracted in 80 % acetone (4053-4064 mg/100 g) and 80 % methanol (11,271-11,370 mg/100 g) respectively. For tannins, maximum extraction was in 80 % acetone (control, 16441 mg/100 g), 80 % ethanol (microwave, 19,558 mg/100 g), and pure methanol (roasted, 15,823 mg/100 g). Total phenol and flavonoid contents were positively associated with AA determined using RP and FRSA. In conclusion, clove exhibited powerful AA in different extraction solvents which increased on dry heat treatments and correlated positively with antioxidant components. Hence, clove can be used as a natural antioxidant in food systems.

  4. Extraction of tetra-oxo anions into a hydrophobic, ionic liquid-based solvent without concomitant ion exchange.

    Energy Technology Data Exchange (ETDEWEB)

    Stepinski, D. C.; Vandegrift, G. F.; Shkrob, I. A.; Wishart, J. F.; Kerr, K.; Dietz, M. L.; Qadah, D. T. D.; Garvey, S. L.; BNL; Univ. of Wisconsin at Milwaukee

    2010-06-16

    Hydrophobic ionic liquids (IL) have the potential to simplify certain separations by serving as both an extraction solvent and an electrolyte for subsequent electrochemical reductions. While IL-based solvents are known to be efficient media for metal ion extraction, separations employing these solvents are frequently complicated by the loss of constituent IL ions to the aqueous phase, resulting in deteriorating performance. In this study, we have examined the extraction of pertechnetate and related tetra-oxo anions from aqueous solutions into IL-based solvents incorporating tetraalkylphosphonium bis[(trifluoromethyl)sulfonyl]imide and a crown ether. In contrast to various previously studied IL-based cation extraction systems, facile anion extraction without significant transfer of the IL ions to the aqueous phase has been observed. In addition, the solvents exhibit high distribution ratios (100-500 for pertechnetate), significant electrical conductivity (>100 ?S/cm), and a wide (4 V) electrochemical window. The results suggest that these solvents may provide the basis for improved approaches to the extraction and recovery of a variety of anions.

  5. Extraction of Tetra-oxo Anions into a Hydrophobic, Ionic Liquid-Based Solvent Without Concomitant Ion Exchange

    Energy Technology Data Exchange (ETDEWEB)

    Stepinski, D.C.; Wishart, J.; Vandegrift, III, G.F.; Shkrob, I.A.; Kerr, K.; Dietz, M.L.; Qadah, D.T.D.; Garvey, S.L.

    2010-06-10

    Hydrophobic ionic liquids (IL) have the potential to simplify certain separations by serving as both an extraction solvent and an electrolyte for subsequent electrochemical reductions. While IL-based solvents are known to be efficient media for metal ion extraction, separations employing these solvents are frequently complicated by the loss of constituent IL ions to the aqueous phase, resulting in deteriorating performance. In this study, we have examined the extraction of pertechnetate and related tetra-oxo anions from aqueous solutions into IL-based solvents incorporating tetraalkylphosphonium bis[(trifluoromethyl)sulfonyl]imide and a crown ether. In contrast to various previously studied IL-based cation extraction systems, facile anion extraction without significant transfer of the IL ions to the aqueous phase has been observed. In addition, the solvents exhibit high distribution ratios (100-500 for pertechnetate), significant electrical conductivity (>100 {micro}S/cm), and a wide ({approx}4 V) electrochemical window. The results suggest that these solvents may provide the basis for improved approaches to the extraction and recovery of a variety of anions.

  6. Biological Activity of Tannins from Acacia mangium Bark Extracted by Different Solvents

    Directory of Open Access Journals (Sweden)

    E. Wina

    2010-08-01

    Full Text Available Acacia mangium bark is abundant byproduct of wood industry in Indonesia. It is underutilized and mainly used as fire wood for the wood industry. The bark contains high level of tannin but the tannin has not been extracted or produced commercially. Tannin isolate can be used for several purposes such as tanning agent for leather, adhesive for plywood or particle board, etc. In ruminant, tannin can be detrimental but can also be beneficial. This experiment was aimed of getting the highest yield of tannin extract with the highest biological activity in rumen fermentation. Nine different solvents at different temperatures were used to extract tannin from A. mangium bark. The extracts were analyzed for their tannin contents and biological activities. Tannin content was analyzed using folin ciocalteau and butanol-HCl methods. Biological activity was described as a percentage of an increase in gas production in the in vitro rumen-buffer fermentation, with and without addition of PEG. The results show that Na2SO3 solution extracted more tannin than other solutions and the higher the concentration of Na2SO3 solution, the higher the yield of tannin extract. The solution of 6% sodium sulphite gave the highest yield of tannin extract (31.2% of original bark sample and the highest concentration of tannin (18.26% but produced a negative effect on in vitro fermentation (% increase of gas production = 2.70%. Extraction with 50% acetone gave a high yield of extract (22.28% of original bark which contained 12.98% of tannin and showed the highest biological response (% increase of gas production = 216%. In conclusion, sodium sulphite solution is not recommended for tannin extraction if the tannin will be used as feed additive in ruminant feed; on the other hand, the aqueous acetone (50% acetone solution is a better choice to be used.

  7. Efficiency of solvent extraction methods for the determination of methyl mercury in forest soils.

    Science.gov (United States)

    Qian, J; Skyllberg, U; Tu, Q; Bleam, W F; Frech, W

    2000-07-01

    Methyl mercury was determined by gas chromatography, microwave induced plasma, atomic emission spectrometry (GC-MIP-AES) using two different methods. One was based on extraction of mercury species into toluene, pre-concentration by evaporation and butylation of methyl mercury with a Grignard reagent followed by determination. With the other, methyl mercury was extracted into dichloromethane and back extracted into water followed by in situ ethylation, collection of ethylated mercury species on Tenax and determination. The accuracy of the entire procedure based on butylation was validated for the individual steps involved in the method. Methyl mercury added to various types of soil samples showed an overall average recovery of 87.5%. Reduced recovery was only caused by losses of methyl mercury during extraction into toluene and during pre-concentration by evaporation. The extraction of methyl mercury added to the soil was therefore quantitative. Since it is not possible to directly determine the extraction efficiency of incipient methyl mercury, the extraction efficiency of total mercury with an acidified solution containing CuSO4 and KBr was compared with high-pressure microwave acid digestion. The solvent extraction efficiency was 93%. For the IAEA 356 sediment certified reference material, mercury was less efficiently extracted and determined methyl mercury concentrations were below the certified value. Incomplete extraction could be explained by the presence of a large part of inorganic sulfides, as determined by x-ray absorption near-edge structure spectroscopy (XANES). Analyses of sediment reference material CRM 580 gave results in agreement with the certified value. The butylation method gave a detection limit for methyl mercury of 0.1 ng g(-1), calculated as three times the standard deviation for repeated analysis of soil samples. Lower values were obtained with the ethylation method. The precision, expressed as RSD for concentrations 20 times above the

  8. CERN Accelerator School - Beam injection, extraction and transfer

    CERN Multimedia

    2016-01-01

    Registration is now open for the CERN Accelerator School’s specialised course to be held in Erice, Italy, from 10 to 19 March, 2017.   The course will be of interest to staff and students in accelerator laboratories, university departments and companies manufacturing accelerator who wish to learn about accelerator science and technology. Further information can be found at: http://indico.cern.ch/event/451905/ http://cas.web.cern.ch/cas/IET2017/IET-advert.html

  9. Synergistic extraction and separation of Co(II)/Ni(II) by solvent extraction technique using TIOA/TOPO as carriers

    Science.gov (United States)

    Okatan, Ahmet; Eyüpoǧlu, Volkan; Kumbasar, Recep Ali; Turgut, Halil Ibrahim

    2016-04-01

    Cobalt and its compounds have wide range applications in some industrial and technological fields. These metals show excellent resistance to oxidation and corrosion under extreme conditions. However, these metals found together within metal ores in nature. This situation makes their separation difficult from each other. They have very similar physical and chemical properties making them very hard to be purified with using traditional separation pathways. Moreover, increasing supply-demand gap between them and decreasing valuable ores because of limited deposit in earth crust have been limited the sources of them. Under the light of this knowledge, one of the practical solutions should be produced to recycle cobalt and nickel from solid and liquid waste containing trace amounts of them. In this study, we investigated the selective and the synergistic cobalt extraction from acidic aqueous solutions by solvent extraction using tri-iso-octylamine (TIOA) and Tri-n-octyl phosphine oxide (TOPO) as carriers. The effective parameters on the extraction and the stripping of the cobalt were investigated, and optimum synergistic extraction and stripping conditions were identified. The cobalt extraction from aqueous Co/Ni solutions in various molar concentrations was examined in the optimum conditions to determine the synergism between TIOA and TOPO.

  10. Extractive-transesterification of algal lipids under microwave irradiation with hexane as solvent.

    Science.gov (United States)

    Martinez-Guerra, Edith; Gude, Veera Gnaneswar; Mondala, Andro; Holmes, William; Hernandez, Rafael

    2014-03-01

    This study describes the use of microwaves (MW) for enhanced extractive-transesterification of algal lipids from dry algal biomass (Chlorella sp.). Two different single-step extractive-transesterification methods under MW irradiation were evaluated: (1) with ethanol as solvent/reactant and sodium hydroxide catalyst; and (2) with ethanol as reactant and hexane as solvent (sodium hydroxide catalyst). Biodiesel (fatty-acid-ethyl-esters, FAEE) yields from these two methods were compared with the conventional Bligh and Dyer (BD) method which followed a two-step extraction-transesterification process. The maximum lipid yields for MW, MW with hexane and BD methods were 20.1%, 20.1%, and 13.9%, respectively; while the FAEE conversion of the algal lipids were 96.2%, 94.3%, and 78.1%, respectively. The algae-biomass:ethanol molar ratio of 1:250-500 and 2.0-2.5% catalyst with reaction times around 6min were determined as optimum conditions for both methods. This study confers that the single-step non-conventional methods can contribute to higher algal lipid and FAEE yields.

  11. Solvent Extraction and QSPR of Catecholamines with a Bis(2-ethlhexyl) Hydrogen Phosphate

    Energy Technology Data Exchange (ETDEWEB)

    Yoshizuka, Kazuharu.; Fujimoto, Yuko.; Ota, Keisuke.; Inoue, Katsutoshi. [Saga University, Saga (Japan). Dept. of Applied Chemistry

    1999-02-01

    In order to develop an effective separation recess for catecholamine (CA), a basic investigation on solvent extraction of dopamine (DA), adrenaline (Ad) and noradrenaline (NA) from hydrochloric acid solution and their stripping is conducted at 30 degree C employing bis(2-ethylhexyl) hydrogen phosphate (D2EHPA) in chloroform, n-hexane and toluene as the organic diluents. From the dependencies of the distribution ratios on the concentrations of reactant species, i.e. CA, hydrogen ion and D2EHPA, it is elucidated that CA (RNH{sub 2}) is extracted with D2EHPA (HR`) according to the ion exchange mechanism, as the complex type, RNH{sub 3}R` (HR`){sub 3}, and the equilibrium constants (K{sub ex,CA}) for the extraction reactions are also evaluated. The quantitative structure property relationship (QSPR) of K{sub ex,CA} values for each organic diluent is discussed using molecular modeling with semi-empirical molecular orbital calculations considering the solvent effect. (author)

  12. 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.

  13. Dispersion-free solvent extraction of Cr(VI) from acidic solutions using hollow fiber contactor.

    Science.gov (United States)

    Alguacil, Francisco J; Alonso, Manuel; Lopez, Félix A; Lopez-Delgado, Aurora; Padilla, Isabel

    2009-10-15

    The use of dispersión-free solvent extraction, through microporous hydrophobic membrane has been investigated. The hollow fiber contactor, with surface area of 1.4 m2 was used to extract Cr(VI) (0.005-0.12 g/L from aqueous sulphuric acidic media (pH 2.5-4.2 +/- 0.05). Several parameters such as extractant concentration, feed acidity and metal concentration in the initial aqueous solution were investigated. Results revealed that 15% v/v Cyanex 923 in Exxsol D-100 as organic phase and feed in the 2.5 pH range, gave optimum extraction (exceeding 95%) of Cr(VI) and it was possible to strip using 10 g/L hydrazine sulfate (also with recoveries exceeding 95%). In this step, Cr(VI) is immediately reduced to the less hazardous Cr(III) state. Results also showed that under the various experimental conditions, chromium(VI) extraction was rate-controlled by the interfacial reaction on the membrane surface. Typical overall mass transfer coefficients values are 4.2 x 10(-5) and 3.6 x 10(-6) cm/s for extraction and stripping operations, respectively.

  14. Antioxidant and antimicrobial activities of the essential oil and solvent extracts of Mentha pulegium L.

    Directory of Open Access Journals (Sweden)

    Palić Ivan R.

    2015-01-01

    Full Text Available We report the total phenolic (TPC; expressed as gallic acid equivalents, GAE, per milligram of dry extract weight and the total flavonoid contents (TFC; expressed as quercetin equivalents, QE, per milligram of dry extract weight and antimicrobial and antioxidant activities of the essential oil and hexane, diethyl ether, ethyl acetate and methanol extracts of Mentha pulegium L. (Lamiaceae collected in Serbia. The total phenolic content was in the range of 129.43-388.29 μg GAE/mg, while TFC ranged from 57.81 to 160.94 QE/mg; the highest TPC and TFC were found in the methanol extract. The antimicrobial activity (against five bacteria and two fungi species of the essential oil and solvent extracts was assessed using disc-diffusion method. However, the studied samples demonstrated a poor antimicrobial potential. The antioxidant activity was screened using five different tests: 2,2-diphenyl-1-picrylhydrazyl radical scavenging assay (DPPH, 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid radical cation decolorization assay (ABTS, total reducing power (TRP, ferric reducing antioxidant power (FRAP and cupric reducing antioxidant capacity assay (CUPRAC; the methanol extract showed the strongest antioxidant potential. The results of the different antioxidant assays were correlated mutually and with the total flavonoid and total phenolic contents (regression analysis and agglomerative hierarchical clustering. [Projekat Ministarstva nauke Republike Srbije, br. 172047

  15. Evaluation of various solvent systems for lipid extraction from wet microalgal biomass and its effects on primary metabolites of lipid-extracted biomass.

    Science.gov (United States)

    Ansari, Faiz Ahmad; Gupta, Sanjay Kumar; Shriwastav, Amritanshu; Guldhe, Abhishek; Rawat, Ismail; Bux, Faizal

    2017-06-01

    Microalgae have tremendous potential to grow rapidly, synthesize, and accumulate lipids, proteins, and carbohydrates. The effects of solvent extraction of lipids on other metabolites such as proteins and carbohydrates in lipid-extracted algal (LEA) biomass are crucial aspects of algal biorefinery approach. An effective and economically feasible algae-based oil industry will depend on the selection of suitable solvent/s for lipid extraction, which has minimal effect on metabolites in lipid-extracted algae. In current study, six solvent systems were employed to extract lipids from dry and wet biomass of Scenedesmus obliquus. To explore the biorefinery concept, dichloromethane/methanol (2:1 v/v) was a suitable solvent for dry biomass; it gave 18.75% lipids (dry cell weight) in whole algal biomass, 32.79% proteins, and 24.73% carbohydrates in LEA biomass. In the case of wet biomass, in order to exploit all three metabolites, isopropanol/hexane (2:1 v/v) is an appropriate solvent system which gave 7.8% lipids (dry cell weight) in whole algal biomass, 20.97% proteins, and 22.87% carbohydrates in LEA biomass. Graphical abstract: Lipid extraction from wet microalgal biomass and biorefianry approach.

  16. Microwave accelerated selective Soxhlet extraction for the determination of organophosphorus and carbamate pesticides in ginseng with gas chromatography/mass spectrometry.

    Science.gov (United States)

    Zhou, Ting; Xiao, Xiaohua; Li, Gongke

    2012-07-03

    Microwave accelerated selective Soxhlet extraction (MA-SSE), a novel selective extraction technique, was investigated in this study. A Soxhlet extraction system containing a glass filter was designed as an extractor. During the procedure of MA-SSE, both the target analytes and the interfering components were extracted from the sample into the extraction solvent enhanced by microwave irradiation. After the solvent flowed though the sorbent, the interfering components were adsorbed by the sorbent, and the target analytes remaining in the solvent were collected in the extraction bottle. No cleanup or filtration was required after extraction. The efficiency of the MA-SSE approach was demonstrated in the determination of organophosphorus and carbamate pesticide residues in ginseng by gas chromatography/mass spectrometry (GC/MS). Under the optimized conditions, low limits of detection (0.050-0.50 μg/kg) were obtained. The recoveries were in the range of 72.0-110.1% with relative standard deviations less than 7.1%. Because of the effect of microwave irradiation, MA-SSE showed significant advantage compared with other extraction techniques. The sorbent used in this study showed good cleanup ability. The mechanism of MA-SSE was demonstrated to be based on the rupture of the cell walls according to the structural changes of ginseng samples. On the basis of the results, MA-SSE as a simple and effective sample preparation technique for the analysis of pesticide residues in complex matrixes shows great promise.

  17. Extraction of DNA by magnetic ionic liquids: tunable solvents for rapid and selective DNA analysis.

    Science.gov (United States)

    Clark, Kevin D; Nacham, Omprakash; Yu, Honglian; Li, Tianhao; Yamsek, Melissa M; Ronning, Donald R; Anderson, Jared L

    2015-02-03

    DNA extraction represents a significant bottleneck in nucleic acid analysis. In this study, hydrophobic magnetic ionic liquids (MILs) were synthesized and employed as solvents for the rapid and efficient extraction of DNA from aqueous solution. The DNA-enriched microdroplets were manipulated by application of a magnetic field. The three MILs examined in this study exhibited unique DNA extraction capabilities when applied toward a variety of DNA samples and matrices. High extraction efficiencies were obtained for smaller single-stranded and double-stranded DNA using the benzyltrioctylammonium bromotrichloroferrate(III) ([(C8)3BnN(+)][FeCl3Br(-)]) MIL, while the dicationic 1,12-di(3-hexadecylbenzimidazolium)dodecane bis[(trifluoromethyl)sulfonyl]imide bromotrichloroferrate(III) ([(C16BnIM)2C12(2+)][NTf2(-), FeCl3Br(-)]) MIL produced higher extraction efficiencies for larger DNA molecules. The MIL-based method was also employed for the extraction of DNA from a complex matrix containing albumin, revealing a competitive extraction behavior for the trihexyl(tetradecyl)phosphonium tetrachloroferrate(III) ([P6,6,6,14(+)][FeCl4(-)]) MIL in contrast to the [(C8)3BnN(+)][FeCl3Br(-)] MIL, which resulted in significantly less coextraction of albumin. The MIL-DNA method was employed for the extraction of plasmid DNA from bacterial cell lysate. DNA of sufficient quality and quantity for polymerase chain reaction (PCR) amplification was recovered from the MIL extraction phase, demonstrating the feasibility of MIL-based DNA sample preparation prior to downstream analysis.

  18. Impact of solvent extraction organics on adsorption and bioleaching of A. ferrooxidans and L. ferriphilum

    Science.gov (United States)

    Hualong, Yu; Xiaorong, Liu

    2017-04-01

    Copper solvent extraction entrained and dissoluted organics (SX organics) in the raffinate during SX operation can contaminated chalcopyrite ores and influence bioleaching efficiency by raffinate recycling. The adsorption and bioleaching of A. ferrooxidans and L. ferriphilum with contaminated ores were investigated. The results showed that, A. ferrooxidans and L. ferriphilum cells could adsorb quickly on minerals, the adsorption rate on contaminated ores were 83% and 60%, respectively, larger than on uncontaminated ores. However, in the bioleaching by the two kinds of acid bacterias, contaminated ores presented a lower bioleaching efficiency.

  19. Demonstration of Caustic-Side Solvent Extraction with Savannah River Site High Level Waste

    Energy Technology Data Exchange (ETDEWEB)

    Walker, D.D.

    2001-08-27

    Researchers successfully demonstrated the chemistry and process equipment of the Caustic-Side Solvent Extraction (CSSX) flowsheet for the decontamination of high level waste using a 33-stage, 2-cm centrifugal contactor apparatus at the Savannah River Technology Center. This represents the first CSSX process demonstration using Savannah River Site (SRS) high level waste. Three tests lasting 6, 12, and 48 hours processed simulated average SRS waste, simulated Tank 37H/44F composite waste, and Tank 37H/44F high level waste, respectively.

  20. DEVELOPMENT OF CONTINUOUS SOLVENT EXTRACTION PROCESSES FOR COAL DERIVED CARBON PRODUCTS

    Energy Technology Data Exchange (ETDEWEB)

    Elliot B. Kennel; Stephen P. Carpenter; Dady Dadyburjor; Manoj Katakdaunde; Liviu Magean; Madhavi Nallani-Chakravartula; Peter G. Stansberry; Alfred H. Stiller; John W. Zondlo

    2006-03-27

    The purpose of this DOE-funded effort is to develop continuous processes for solvent extraction of coal for the production of carbon products. These carbon products include materials used in metals smelting, especially in the aluminum and steel industries, as well as porous carbon structural material referred to as ''carbon foam'' and carbon fibers. During this reporting period, efforts have focused on the development of continuous processes for hydrogenation as well as continuous production of carbon foam and coke.

  1. DEVELOPMENT OF CONTINUOUS SOLVENT EXTRACTION PROCESSES FOR COAL DERIVED CARBON PRODUCTS

    Energy Technology Data Exchange (ETDEWEB)

    Elliot B. Kennel; Stephen P. Carpenter; Dady Dadyburjor; Manoj Katakdaunde; Liviu Magean; Peter G. Stansberry; Alfred H. Stiller; John W. Zondlo

    2005-06-08

    The purpose of this DOE-funded effort is to develop continuous processes for solvent extraction of coal for the production of carbon products. These carbon products include materials used in metals smelting, especially in the aluminum and steel industries, as well as porous carbon structural material referred to as ''carbon foam'' and carbon fibers. During this reporting period, efforts have focused on the development of continuous processes for hydrogenation as well as continuous production of carbon foam and coke.

  2. DEVELOPMENT OF CONTINUOUS SOLVENT EXTRACTION PROCESSES FOR COAL DERIVED CARBON PRODUCTS

    Energy Technology Data Exchange (ETDEWEB)

    Elliot B. Kennel; Stephen P. Carpenter; Dady Dadyburjor; Manoj Katakdaunde; Liviu Magean; Peter G. Stansberry; Alfred H. Stiller; John W. Zondlo

    2005-08-11

    The purpose of this DOE-funded effort is to develop continuous processes for solvent extraction of coal for the production of carbon products. These carbon products include materials used in metals smelting, especially in the aluminum and steel industries, as well as porous carbon structural material referred to as ''carbon foam'' and carbon fibers. During this reporting period, efforts have focused on the facility modifications for continuous hydrotreating, as well as developing improved protocols for producing synthetic pitches.

  3. Antioxidant, Antimicrobial Properties and Phenolics of Different Solvent Extracts from Bark, Leaves and Seeds of Pongamia pinnata (L.) Pierre

    OpenAIRE

    Alkharfy, Khalid M; Anwarul-Hassan Gilani; Ghulam Rasul; Ghulam Shabir; Farooq Anwar; Zahid Iqbal Sajid

    2012-01-01

    This study appraises the antioxidant and antimicrobial attributes of various solvent extracts (absolute methanol, aqueous methanol, absolute ethanol, aqueous ethanol, absolute acetone, aqueous acetone, and deionized water) from bark, leaves and seeds of Pongamia pinnata (L.) Pierre. Maximum extraction yield of antioxidant components from bark (16.31%), leaves (11.42%) and seeds (21.51%) of P. pinnata was obtained using aqueous methanol (20:80). Of the extracts tested, the bark extract, obtain...

  4. The Extraction Process of Trimethyl Xanthina in Vitro Culture of Callus Camellia Sinensis with ethyl Acetate Solvent

    Directory of Open Access Journals (Sweden)

    Sutini

    2016-01-01

    Full Text Available Trimethyl xanthina is one of the compounds contained bioactive culture in vitro Cammelia sinensis callus which is widely used in the field of food, beverage, agriculture and health industries. The presence of trimethyl xanthina on food, beverages and health is needed in a certain amount depending on the use which is achieved by the user. To get a certain amount of trimethyl xanthina from callus culture of Cammelia sinensis, the extraction process is performed on the water solvent, as well as non-solvent water / organic solvent such as ethyl acetate. The purpose of this study was to obtain profile of trimethyl xanthina in the extraction of Cammelia sinensis callus. The experimental methods used consisted of dissolution, filtration, extraction with water solvent and ethyl acetate, then followed by identification of trimethyl xanthina using HPLC. The results shows the profile form of trimethyl xanthina of Cammelia sinensis callus have similarities with the standard form of trimethyl xanthina.

  5. A combination of solvent extraction and freeze thaw for oil recovery from petroleum refinery wastewater treatment pond sludge.

    Science.gov (United States)

    Hu, Guangji; Li, Jianbing; Hou, Haobo

    2015-01-01

    A combination of solvent extraction and freeze thaw was examined for recovering oil from the high-moisture petroleum refinery wastewater treatment pond sludge. Five solvents including cyclohexane (CHX), dichloromethane (DCM), methyl ethyl ketone (MEK), ethyl acetate (EA), and 2-propanol (2-Pro) were examined. It was found that these solvents except 2-Pro showed a promising oil recovery rate of about 40%, but the recycling of DCM solvent after oil extraction was quite low. Three solvents (CHX, MEK and EA) were then selected for examining the effect of freeze/thaw treatment on improving the quality of recovered oil. This treatment increased the total petroleum hydrocarbon (TPH) content in recovered oil from about 40% to 60% for both MEK and EA extractions, but little effect was observed for CHX extraction. Although the solid residue after oil recovery had a significantly decreased TPH content, a high concentration of heavy metals was observed, indicating that this residue may require proper management. In general, the combination of solvent extraction with freeze/thaw is effective for high-moisture oily hazardous waste treatment.

  6. Effect of biomass pre-treatment and solvent extraction on beta-carotene and lycopene recovery from Blakeslea trispora cells.

    Science.gov (United States)

    Papaioannou, E; Roukas, T; Liakopoulou-Kyriakides, M

    2008-01-01

    The production of carotenoids from Blakeslea trispora cells in a synthetic medium has been reported, with the main products being beta-carotene, lycopene, and gamma-carotene. The effect of biomass pretreatment and solvent extraction on their selective recovery is reported here. Eight solvents of class II and III of the International Conference of Harmonization: ethanol, methanol, acetone, 2-propanol, pentane, hexane, ethyl acetate, and ethyl ether, and HPLC analysis were used for the evaluation of their selectivities towards the three main carotenoids with regard to different biomass pre-treatment. The average C(max) values (maximum concentration of caronoids in a specific solvent) were estimated to 16 mg/L with the five out of eight solvents investigated, whereas methanol, pentane, and hexane gave lower values of 10, 11, and 9 mg/L, respectively. The highest carotenoid yield was obtained in the case of wet biomass, where 44-56% is recovered with one solvent and three extractions and the rest is recovered only after subsequent treatment with acetone; thus, four extractions of 2.5 h are needed. Two extractions of 54 min are enough to recover carotenoids from dehydrated biomass, with the disadvantage of a high degree of degradation. Our results showed that, for maximum carotenoid recovery, ethyl ether, 2-propanol, and ethanol could be successfully used with biomass without prior treatment, whereas fractions enriched in beta-carotene or lycopene can be obtained by extraction with the proper solvent, thus avoiding degradation due to time-consuming processes.

  7. Two stage leaching of activated spent HDS catalyst and solvent extraction of aluminium using organo-phosphinic extractant, Cyanex 272.

    Science.gov (United States)

    Park, Kyung Ho; Mohapatra, Debasish; Nam, Chul-Woo

    2007-09-05

    Spent catalyst generally contains valuable metals like Mo, Co, Ni on a supporting material, such as gamma-A1(2)O(3). In the present study, a two stage alkali/acid leaching process is proposed to selectively target molybdenum and cobalt/nickel separately to facilitate the downstream processing. Prior to the leaching, the spent catalyst was calcined at 500 degrees C to remove C and S; and to convert metal sulphides to metal oxides. 98% Mo, 93% Co and 90% Ni was effectively recovered by this process. The sulphuric acid leaching of spent catalyst, previously treated by alkali solutions to remove Mo, yielded a solution rich in Ni, Co and Al. In order to recover Co and Ni, the Al impurity must be eliminated. The extraction and stripping of Al has been carried out using the organo-phosphinic extractant, Cyanex 272 diluted in carbon tetrachloride. Quantitative Al extraction efficiency was achieved with 1.0M Cyanex 272 in two stages at an aqueous:organic (A:O) phase ratio of 1:1 and equilibrium pH of 3.2. Complete stripping of Al from the loaded organic was carried out using 2M H(2)SO(4) at an A:O phase ratio of 1:1. The extraction reaction proceeded via the cation exchange mechanism and the extracted species was assumed to be AlA(3).3HA. The extraction of Al was carried out in the presence of various ions to ascertain the tolerance limit of individual ions. The regenerated solvent was successfully used for 8 cycles without any significant loss of extraction efficiency, suggesting that Cyanex 272 is extremely stable under present experimental conditions.

  8. Unraveling Entropic Rate Acceleration Induced by Solvent Dynamics in Membrane Enzymes.

    Science.gov (United States)

    Kürten, Charlotte; Syrén, Per-Olof

    2016-01-16

    Enzyme catalysis evolved in an aqueous environment. The influence of solvent dynamics on catalysis is, however, currently poorly understood and usually neglected. The study of water dynamics in enzymes and the associated thermodynamical consequences is highly complex and has involved computer simulations, nuclear magnetic resonance (NMR) experiments, and calorimetry. Water tunnels that connect the active site with the surrounding solvent are key to solvent displacement and dynamics. The protocol herein allows for the engineering of these motifs for water transport, which affects specificity, activity and thermodynamics. By providing a biophysical framework founded on theory and experiments, the method presented herein can be used by researchers without previous expertise in computer modeling or biophysical chemistry. The method will advance our understanding of enzyme catalysis on the molecular level by measuring the enthalpic and entropic changes associated with catalysis by enzyme variants with obstructed water tunnels. The protocol can be used for the study of membrane-bound enzymes and other complex systems. This will enhance our understanding of the importance of solvent reorganization in catalysis as well as provide new catalytic strategies in protein design and engineering.

  9. Solvent Extraction of Copper: An Extractive Metallurgy Exercise for Undergraduate Teaching Laboratories

    Science.gov (United States)

    Smellie, Iain A.; Forgan, Ross S.; Brodie, Claire; Gavine, Jack S.; Harris, Leanne; Houston, Daniel; Hoyland, Andrew D.; McCaughan, Rory P.; Miller, Andrew J.; Wilson, Liam; Woodhall, Fiona M.

    2016-01-01

    A multidisciplinary experiment for advanced undergraduate students has been developed in the context of extractive metallurgy. The experiment serves as a model of an important modern industrial process that combines aspects of organic/inorganic synthesis and analysis. Students are tasked to prepare a salicylaldoxime ligand and samples of the…

  10. Online determination of copper in aluminum alloy by microchip solvent extraction using isotope dilution ICP-MS method.

    Science.gov (United States)

    Kagawa, Tsuyoshi; Ohno, Masashi; Seki, Tatsuya; Chikama, Katsumi

    2009-09-15

    Isotope dilution mass spectroscopy (IDMS)/ICP-MS combined with microchip solvent extraction was successfully applied for the online determination of copper in an aluminum alloy. The microchip solvent extraction was developed for the separation of Cu from major element, and optimal pH range was wider than that of the batchwise extraction method. The dimensions of the microchip were 30 mm x 70 mm and that of micro-channel on the microchip was 180 microm wide and 40 microm deep. The copper complex with 8-hydroxyquinoline was extracted into o-xylene at pH 5.5 and back extracted with 0.1 mol l(-1) nitric acid at flow rate of 20 microl min(-1). The total extraction efficiency (water/organic solvent/nitric acid) was around 40%. IDMS/ICP-MS was coupled with solvent extraction for precise determination of Cu. The extraction and back-extraction on the microchip took about 1s and the total measurement time for the IDMS/ICP-MS was about 40s/sample. The blank value of this method was 0.1 ng g(-1). The proposed method was used for the determination of Cu in Al standard materials (JSAC 0121-C, The Japan Society for Analytical Chemistry and 7074 Al alloy, Nippon Light Metal Co. Ltd.). The obtained analytical results are in good agreement with the certified values.

  11. Supercritical fluid extraction: spectroscopic study of interactions comparison to solvent extraction

    Energy Technology Data Exchange (ETDEWEB)

    Rustenholtz Farawila, A

    2005-06-15

    Supercritical fluid carbon dioxide (SF-CO{sub 2}) was chosen to study Supercritical Fluid Extraction (SFE) of cesium and uranium. At first, crown ethers were considered as chelating agents for the SFE of cesium. The role of water and its interaction with crown ethers were especially studied using Fourier-Transform Infra-Red (FT-IR) spectroscopy in SF-CO{sub 2}. A sandwich configuration between two crown ethers and a water molecule was observed in the SF-CO{sub 2} phase for the first time. The equilibrium between the single and the bridge configurations was defined. The enthalpy of the hydrogen bond formation was also calculated. These results were then compared to the one in different mixtures of chloroform and carbon tetra-chloride using Nuclear Magnetic Resonance (NMR). To conclude this first part and in order to understand the whole picture of the recovery of cesium, I studied the role of water in the equilibrium between the cesium and the di-cyclo-hexano18-crown-6.In a second part, the supercritical fluid extraction of uranium was studied in SF-CO{sub 2}. For this purpose, different complexes of Tributyl Phosphate (TBP), nitric acid and water were used as chelating and oxidizing agents. I first used FT-IR to study the TBP-water interaction in SF-CO{sub 2}. These results were then compared to the one obtained with NMR in chloroform. NMR spectroscopy was also used to understand the TBP-nitric acid-water interaction first alone and then in chloroform. To conclude my research work, I succeeded to improve the efficiency of uranium extraction and stripping into water for a pilot-plant where enriched uranium is extracted from incinerated waste coming from nuclear fuel fabrication. TBP-nitric acid complexes were used in SF-CO{sub 2} for the extraction of uranium from ash. (author)

  12. DEVELOPMENT OF CONTINUOUS SOLVENT EXTRACTION PROCESSES FOR COAL DERIVED CARBON PRODUCTS

    Energy Technology Data Exchange (ETDEWEB)

    Elliot B. Kennel; Philip L. Biedler; Chong Chen; Dady Dadyburjor; Liviu Magean; Peter G. Stansberry; Alfred H. Stiller; John W. Zondlo

    2005-04-13

    The purpose of this DOE-funded effort is to develop continuous processes for solvent extraction of coal for the production of carbon products. These carbon products include materials used in metals smelting, especially in the aluminum and steel industries, as well as porous carbon structural material referred to as ''carbon foam'' and carbon fibers. A process has been developed which results in high quality binder pitch suitable for use in graphite electrodes or carbon anodes. A detailed description of the protocol is given by Clendenin. Briefly, aromatic heavy oils are hydro-treated under mild conditions in order to increase their ability to dissolve coal. An example of an aromatic heavy oil is Koppers Carbon Black Base (CBB) oil. CBB oil has been found to be an effective solvent and acceptably low cost (i.e., significantly below the market price for binder pitch, or about $280 per ton at the time of this writing). It is also possible to use solvents derived from hydrotreated coal and avoid reliance on coke oven recovery products completely if so desired.

  13. Extraction of lignins from aqueous-ionic liquid mixtures by organic solvents.

    Science.gov (United States)

    Xin, Qin; Pfeiffer, Katie; Prausnitz, John M; Clark, Douglas S; Blanch, Harvey W

    2012-02-01

    The commercial development of ionic liquids (ILs) to pretreat lignocellulose by dissolution of whole biomass and cellulose precipitation by addition of water is hindered by the absence of an effective technique to recover the lignin content of the biomass from the IL. Three organic solvents [ethyl acetate, 1,4-dioxane, and tetrahydrofuran (THF)] were studied for their ability to form a two-liquid-phase system with water and 1-ethyl-3-methylimidazolium acetate ([C(2)mim][OAc]), and for partitioning model lignins and lignin monomers between the two liquid phases. Ternary diagrams were obtained for three [C(2)mim][OAc]/organic solvent/water systems at 22°C. Partition coefficients were measured for several types of lignin in these three systems. Partition coefficients increase with rising water content in the IL phase, and depend strongly on the type of lignin and on the organic solvent. Partition coefficients rise as the pH of the ionic-liquid-rich phase falls. Small molecule model lignin monomer compounds (guaiacol, syringaldehyde) are also readily extracted from the IL/water system by THF. Copyright © 2011 Wiley Periodicals, Inc.

  14. Maximizing Lipid Yield in Neochloris oleoabundans Algae Extraction by Stressing and Using Multiple Extraction Stages with N-Ethylbutylamine as Switchable Solvent

    Science.gov (United States)

    2017-01-01

    The extraction yield of lipids from nonbroken Neochloris oleoabundans was maximized by using multiple extraction stages and using stressed algae. Experimental parameters that affect the extraction were investigated. The study showed that with wet algae (at least) 18 h extraction time was required for maximum yield at room temperature and a solvent/feed ratio of 1:1 (w/w). For fresh water (FW), nonstressed, nonbroken Neochloris oleoabundans, 13.1 wt % of lipid extraction yield (based on dry algae mass) was achieved, which could be improved to 61.3 wt % for FW stressed algae after four extractions, illustrating that a combination of stressing the algae and applying the solvent N-ethylbutylamine in multiple stages of extraction results in almost 5 times higher yield and is very promising for further development of energy-efficient lipid extraction technology targeting nonbroken wet microalgae. PMID:28781427

  15. Antioxidant activities of lead (Leucaena leucocephala) seed as affected by extraction solvent, prior dechlorophyllisation and drying methods.

    Science.gov (United States)

    Benjakul, Soottawat; Kittiphattanabawon, Phanat; Sumpavapol, Punnanee; Maqsood, Sajid

    2014-11-01

    Extracts of brown lead (Leucaena leucocephala) seed prepared using different extraction solvents were determined for antioxidative activities using different assays. The highest yield (3.4-4.0%) was obtained when water was used as an extraction solvent, compared with all ethanolic extracts used (1.2-2.0 %) (P < 0.05). Much lower chlorophyll content was found in the water extract. When hot water was used, the resulting extract contained lower total phenolic and mimosine contents (P < 0.05). In general, 60-80 % ethanolic extracts had higher 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) radical scavenging activities, ferric reducing antioxidant power (FRAP) and metal chelating activity than water extracts (P < 0.05). When brown lead seed was dechlorophyllised prior to extraction, the water extract had slightly increased yield with lower chlorophyll content. Nevertheless, prior chlorophyll removal resulted in the increase in antioxidative activities but lower total phenolic and mimosine contents (P < 0.05). Generally, phenolic compounds and mimosine were more released when water was used as the extraction solvent, while the lower amount of chlorophyll was extracted. Oven-drying exhibited the negative effect on antioxidative activities and mimosine content. The higher antioxidative activities with concomitant higher total phenolic and mimosine contents were found in water extract dried by freeze drying. Thus, extraction solvent, dechlorophyllisation and drying methods directly influenced the yield and antioxidative activity of lead seed extract.

  16. Thallium extraction from hydrochloric acid media into a deep eutectic solvent using bis(2-ethylhexyl) phosphate

    Science.gov (United States)

    Tran, Kate; Volia, Merinda; Tereshatov, Evgeny; Folden, Charles, III

    2016-09-01

    The chemical properties of superheavy elements are relatively unknown due to their short half-lives and difficulty of production. In preparation for a future experiment to study the chemical properties of element 113, separation techniques have been used to study the behavior of its homologs, In and Tl. Previous work studied the liquid-liquid extraction of radioactive 201Tl (t1 / 2 = 3 . 04 d) from various concentrations of HCl into a mixture of menthol and lauric acid that formed a so-called deep eutectic solvent (DES). This work focuses on the effects of adding an extraction agent, bis(2-ethylhexyl) phosphate (HDEHP), to the DES on the efficiency of thallium extraction. The extraction of Tl(I) was generally poor, both with and without HDEHP added. In contrast, 111In (t1 / 2 = 2 . 80 d) showed significant extraction using HDEHP added to the same DES. This difference in behavior could potentially be exploited in a future experiment on the chemistry of element 113. National Science Foundation.

  17. Influence of extraction solvent on antioxidant capacity value of oleaster measured by ORAC method.

    Science.gov (United States)

    Yalcin, Gorkem; Sogut, Ozlem

    2014-01-01

    Oxygen radical absorbance capacity (ORAC) is a widely used hydrogen atom transfer-based method which measures the antioxidant capacity of natural products. ORAC values of oleaster (Elaeagnus angustifolia L.), which was extracted with ethanol/acetone (7:3, v/v), ethanol/water (1:1, v/v) and methanol/water (1:1, v/v) in order to evaluate the effects of solvent type on antioxidant capacity, were examined. In general, results revealed that ethanol/water extracts exhibited better antioxidant capacity values. Furthermore, results obtained by using ORAC-eosin y (ORAC-EY), one of the widely used derivative of fluorescein (FL), as a fluorescent probe were compared with those obtained by using ORAC-FL. According to the results, ORAC-EY values were found to be compatible with ORAC-FL values.

  18. Nickel solvent extraction from cold purification filter cakes of Angouran mine concentrate using LIX984N

    Institute of Scientific and Technical Information of China (English)

    AA Balesini; A Zakeri; H Razavizadeh; A Khani

    2013-01-01

    Cold purification filter cakes generated in the hydrometallurgical processing of Angouran mine zinc concentrate commonly contain significant amounts of Zn, Cd, and Ni ions and thus are valuable resources for metal recovery. In this research, a nickel containing solution that was obtained from sulfuric acid leaching of the filter cake following cadmium and zinc removal was subjected to solvent extraction experiments using 10vol%LIX984N diluted in kerosene. Under optimum experimental conditions (pH 5.3, volume ratio of organic/aqueous (O:A) = 2:1, and contact time = 5 min), more than 97.1% of nickel was extracted. Nickel was stripped from the loaded organic by contacting with a 200 g/L sulfuric acid solution, from which 77.7% of nickel was recovered in a single contact at the optimum conditions (pH 1-1.5, O:A = 5:1, and contact time=15 min).

  19. 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.

  20. Sequential solvent extraction for forms of antimony in five selected coals

    Science.gov (United States)

    Qi, C.; Liu, Gaisheng; Kong, Y.; Chou, C.-L.; Wang, R.

    2008-01-01

    Abundance of antimony in bulk samples has been determined in five selected coals, three coals from Huaibei Coalfield, Anhui, China, and two from the Illinois Basin in the United States. The Sb abundance in these samples is in the range of 0.11-0.43 ??g/g. The forms of Sb in coals were studied by sequential solvent extraction. The six forms of Sb are water soluble, ion changeable, organic matter bound, carbonate bound, silicate bound, and sulfide bound. Results of sequential extraction show that silicate-bound Sb is the most abundant form in these coals. Silicate- plus sulfide-bound Sb accounts for more than half of the total Sb in all coals. Bituminous coals are higher in organic matterbound Sb than anthracite and natural coke, indicating that the Sb in the organic matter may be incorporated into silicate and sulfide minerals during metamorphism. ?? 2008 by The University of Chicago. All rights reserved.

  1. Molecular characteristics of Kraft-AQ pulping lignin fractionated by sequential organic solvent extraction.

    Science.gov (United States)

    Wang, Kun; Xu, Feng; Sun, Runcang

    2010-08-16

    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, (13)C-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. SOLVENT EXTRACTION RESEARCH AND DEVELOPMENT IN THE U.S. FUEL CYCLE PROGRAM

    Energy Technology Data Exchange (ETDEWEB)

    Terry A. Todd

    2011-10-01

    Treatment or processing of used nuclear fuel to recycle uranium and plutonium has historically been accomplished using the well known PUREX process. The PUREX process has been used on an industrial scale for over 60 years in the nuclear industry. Research is underway to develop advanced separation methods for the recovery of other used fuel components, such as the minor actinides (Np, Am, Cm) for possible transmutation in fast spectrum reactors, or other constituents (e.g. Cs, Sr, transition metals, lanthanides) to help facilitate effective waste management options. This paper will provide an overview of new solvent extraction processes developed for advanced nuclear fuel cycles, and summarize recent experimental results. This will include the utilization of new extractants for selective separation of target metals and new processes developed to selectively recover one or more elements from used fuel.

  3. Extraction of Cs-137 by alcohol-water solvents from plants containing cardiac glycosides

    CERN Document Server

    Dzyubak, S N; Dzyubak, O P; Sorokin, P V; Popov, V F; Orlov, A A; Krasnov, V P; Gubin, Yu.I.

    2001-01-01

    As a result of nuclear power plant accidents, large areas receive radioactive inputs of Cs-137. This cesium accumulates in herbs growing in such territories. The problem is whether the herbs contaminated by radiocesium may be used as a raw material for medicine. The answer depends on the amount of Cs-137 transfered from the contaminated raw material to the medicine. We have presented new results of the transfer of Cs-137 from contaminated Digitalis grandiflora Mill. and Convallaria majalis L. to medicine. We found that the extraction of Cs-137 depends strongly on the hydrophilicity of the solvent. For example 96.5%(vol.) ethyl alcohol extracts less Cs-137 (11.6%) than 40%(vol.) ethyl alcohol or pure water (66.2%). The solubility of the cardiac glycosides is inverse to the solubility of cesium, which may be of use in the technological processes for manufacturing ecologically pure herbal medicine.

  4. Caustic-Side Solvent-Extraction Modeling for Hanford Interim Pretreatment System

    Energy Technology Data Exchange (ETDEWEB)

    Moyer, B.A.; Birdwell, J.F.; Delmau, L. H.; McFarlane, J.

    2008-06-01

    The purpose of this work is to examine the applicability of the Caustic-Side Solvent Extraction (CSSX) process for the removal of cesium from Hanford tank-waste supernatant solutions in support of the Hanford Interim Pretreatment System (IPS). The Hanford waste types are more challenging than those at the Savannah River Site (SRS) in that they contain significantly higher levels of potassium, the chief competing ion in the extraction of cesium. It was confirmed by use of the CSSX model that the higher levels of potassium depress the cesium distribution ratio (DCs), as validated by measurement of DCs values for four of eight specified Hanford waste-simulant compositions. The model predictions were good to an apparent standard error of ±11%. It is concluded from batch distribution experiments, physical-property measurements, equilibrium modeling, flowsheet calculations, and contactor sizing that the CSSX process as currently employed for cesium removal from alkaline salt waste at the SRS is capable of treating similar Hanford tank feeds. For the most challenging waste composition, 41 stages would be required to provide a cesium decontamination factor (DF) of 5000 and a concentration factor (CF) of 5. Commercial contacting equipment with rotor diameters of 10 in. for extraction and 5 in. for stripping should have the capacity to meet throughput requirements, but testing will be required to confirm that the needed efficiency and hydraulic performance are actually obtainable. Markedly improved flowsheet performance was calculated for a new solvent formulation employing the more soluble cesium extractant BEHBCalixC6 used with alternative scrub and strip solutions, respectively 0.1 M NaOH and 10 mM boric acid. The improved system can meet minimum requirements (DF = 5000 and CF = 5) with 17 stages or more ambitious goals (DF = 40,000 and CF = 15) with 19 stages. Potential benefits of further research and development are identified that would lead to reduced costs, greater

  5. A green analytical chemistry approach for lipid extraction: computation methods in the selection of green solvents as alternative to hexane.

    Science.gov (United States)

    Cascant, Mari Merce; Breil, Cassandra; Garrigues, Salvador; de la Guardia, Miguel; Fabiano-Tixier, Anne Silvie; Chemat, Farid

    2017-05-01

    There is a great interest in finding alternatives and green solvents in extraction processes to replace petroleum based solvents. In order to investigate these possibilities, computational methods, as Hansen solubility parameters (HSP) and conductor-like screening model for real solvent (COSMO-RS), were used in this work to predict the solvation power of a series of solvents in salmon fish lipids. Additionally, experimental studies were used to evaluate the performance in lipids extraction using 2-methyltetrahydrofurane, cyclopentyl methyl ether, dimethyl carbonate, isopropanol, ethanol, ethyl acetate, p-cymene and d-limonene compared with hexane. Lipid classes of extracts were obtained by using high performance thin-layer chromatography (HPTLC), whereas gas chromatography with a flame ionization detector (GC/FID) technique was employed to obtain fatty acid profiles. Some differences between theoretical and experimental results were observed, especially regarding the behavior of p-cymene and d-limonene, which separate from the predicted capability. Results obtained from HPTLC indicated that p-cymene and d-limonene extract triglycerides (TAGs) and diglycerides (DAGs) at levels of 73 and 19%, respectively, whereas the other studied extracts contain between 75 and 76% of TAGs and between 16 and 17% of DAGs. Fatty acid profiles, obtained by using GC-FID, indicated that saturated fatty acids (SFAs) between 19.5 and 19.9% of extracted oil, monounsaturated fatty acids (MUFAs) in the range between 43.5 and 44.9%, and PUFAs between 31.2 and 34.6% were extracted. p-Cymene and limonene extracts contained lower percentages than the other studied solvents of some PUFAs due probably to the fact that these unsaturated fatty acids are more susceptible to oxidative degradation than MUFAs. Ethyl acetate has been found to be the best alternative solvent to hexane for the extraction of salmon oil lipids. Graphical Abstract ᅟ.

  6. Solvent extraction of jojoba oil from pre-pressed jojoba meal

    Directory of Open Access Journals (Sweden)

    El Haron, Dalia E.

    2004-06-01

    Full Text Available The solvent extraction process of jojoba oil from the meal cake obtained after the mechanical pressing of jojoba seeds was studied. Commercial hexane and petroleum ether were used as solvents and the extraction was carried out at temperatures ranging from 30 to 55 °C using solvent-to-solid ratios, R between 2 and 15 L/kg. The equilibrium compositions of the solvent and solid phases were determined. Based on the equilibrium data, the partition coefficient or distribution ratio, D of the oil between both phases was estimated. Also, the number of extraction stages necessary to achieve a certain degree of oil recovery has been determined using different hexane-to-meal ratios. Jojoba oil was also tested for its physical and chemical properties including chemical composition, percentage fatty acid, peroxide value, flash point, fire point, pour point, refractive index, saponification and iodine values. The stability of jojoba oil during storage at room temperature and during heat treatment was also studied.Se ha estudiado el proceso de extracción con disolventes del aceite contenido en la harina residual del prensado mecánico de las semillas de jojoba. Como disolventes se han utilizado hexano técnico y éter de petróleo, habiéndose efectuado extracciones a temperaturas comprendidas entre 30 ºC y 55 ºC , con relaciones de disolvente a sólido, R, de entre 12 y 15 L/kg. Se han determinado las composiciones del extracto y del residuo sólido en el equilibrio y a partir de los datos de equilibrio, se ha estimado el coeficiente de partición o cociente de distribución, D, del aceite entre ambas fases. Asimismo, se ha determinado el número de etapas de extracción necesarias para conseguir un cierto grado de recuperación del aceite, utilizando diferentes relaciones entre hexano y harina. También se han determinado las propiedades físicas y químicas del aceite de jojoba, incluyendo la composición química, el porcentaje de ácidos grasos

  7. MODULAR CAUSTIC SIDE SOLVENT EXTRACTION UNIT GAMMA MONITORS SYSTEM FINAL REPORT

    Energy Technology Data Exchange (ETDEWEB)

    Casella, V

    2007-06-25

    The Department of Energy (DOE) selected Caustic-Side Solvent Extraction (CSSX) as the preferred technology for the removal of radioactive cesium from High-Level Waste (HLW) at the Savannah River Site (SRS). Before the full-scale Salt Waste Processing Facility (SWPF) becomes operational, the liquid Waste Organization (LWO) plans to process a portion of dissolved saltcake waste through a Modular CSSX Unit (MCU). This work was derived from Technical Task Request SP-TTR-2004-00013, ''Gamma Monitor for MCU.'' The deliverables for this task are the hardware and software for the gamma monitors and a report summarizing the testing and acceptance of this equipment for use in the MCU. Revision of this report is a deliverable in Technical Task Report SP-TTR-2006-00010, ''NaI Shield Box Testing.'' Gamma-ray monitors were developed to: {lg_bullet} Measure the Cs-137 concentration in the decontaminated salt solution before entering the DSS (Decontaminated Salt Solution) Hold Tank, {lg_bullet} Measure the Cs-137 concentration in the strip effluent before entering the Strip Effluent Hold Tank, {lg_bullet} Verify proper operation of the solvent extraction system by verifying material balance within the process (The DSS Hold Tank Cs-137 concentration will be very low and the Cs-137 concentration in the Strip Effluent Hold Tank will be approximately fifteen times higher than the Cs-137 concentration in the Feed Tank.)

  8. Recovery of nickel, cobalt, copper and zinc in sulphate and chloride solutions using synergistic solvent extraction

    Institute of Scientific and Technical Information of China (English)

    Chu Yong Cheng; Keith R. Barnard; Wensheng Zhang; Zhaowu Zhu; Yoko Pranolo

    2016-01-01

    A number of synergistic solvent extraction (SSX) systems have been developed to recover nickel, cobalt, zinc and copper from sulphuric and chloride leach solutions by the solvent extraction team of CSIRO, Australia. These in-clude (1) Versatic 10/CLX50 system for the separation of Ni from Ca in sulphate solutions, (2) Versatic 10/4PC system for the separation of Ni and Co from Mn/Mg/Ca in sulphate solutions, (3) Cyanex 471X/HRJ-4277 system for the separation of Zn from Cd in sulphate solutions, (4) Versatic 10/LIX63 system for the separation of Co from Mn/Mg/Ca in sulphate solutions, (5) Versatic 10/LIX63/TBP system for separation of Ni and Co from Mn/Mg/Ca in sulphate solutions, (6) Versatic 10/LIX63 system for the separation of cobalt from nickel in sulphate solutions by difference in kinetics, (7) Cyanex 272/LIX84 system for the separation of Cu/Fe/Zn from Ni/Co in sulphate solutions, (8) Versatic 10/LIX63/TBP system to recover Cu/Ni from strong chloride solutions, and (9) Versatic 10/LIX63 system to separate Cu from Fe in strong chloride solutions. The synergistic effect on metal separation and efficiency is presented and possible industrial applications are demonstrated. The chemical stability of selected SSX systems is also reported.

  9. DEVELOPMENT OF CONTINUOUS SOLVENT EXTRACTION PROCESSES FOR COAL DERIVED CARBON PRODUCTS

    Energy Technology Data Exchange (ETDEWEB)

    Elliot B. Kennel; R. Michael Bergen; Stephen P. Carpenter; Dady Dadyburjor; Manoj Katakdaunde; Liviu Magean; Alfred H. Stiller; W. Morgan Summers; John W. Zondlo

    2006-05-12

    The purpose of this DOE-funded effort is to develop continuous processes for solvent extraction of coal for the production of carbon products. The largest applications are those which support metals smelting, such as anodes for aluminum smelting and electrodes for arc furnaces. Other carbon products include materials used in creating fuels for the Direct Carbon Fuel Cell, metals smelting, especially in the aluminum and steel industries, as well as porous carbon structural material referred to as ''carbon foam'' and carbon fibers. During this reporting period, coking and composite fabrication continued using coal-derived samples. These samples were tested in direct carbon fuel cells. Methodology was refined for determining the aromatic character of hydro treated liquid, based on Nuclear Magnetic Resonance (NMR) and Fourier Transform Infrared (FTIR). Tests at GrafTech International showed that binder pitches produced using the WVU solvent extraction protocol can result in acceptable graphite electrodes for use in arc furnaces. These tests were made at the pilot scale.

  10. Speciation of iron (II) and (III) by using solvent extraction and flame atomic absorption spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Yaman, Mehmet [Department of Chemistry, Science and Arts Faculty, Firat University, Elazig (Turkey)]. E-mail: myaman@firat.edu.tr; Kaya, Gokce [Department of Chemistry, Science and Arts Faculty, Firat University, Elazig (Turkey)

    2005-05-17

    A method for speciation, preconcentration and separation of Fe{sup 2+} and Fe{sup 3+} in different matrices was developed using solvent extraction and flame atomic absorption spectrometry. PAN as complexing reagent for Fe{sup 2+} and chloroform as organic solvent were used. The complex of Fe{sup 2+}-PAN was extracted into chloroform phase in the pH range of 0.75-4.0 and Fe{sup 3+} remains in water phase in the pH range 0.75-1.25. The optimum conditions for maximum recovery of Fe{sup 2+} and minimum recovery of Fe{sup 3+} were determined as pH = 1, the stirring time of 20 min, the PAN amount of 0.5 mg and chloroform volume of 8 mL. The developed method was applied to the determination of Fe{sup 2+} and Fe{sup 3+} in tea infusion, fruit juice, cola and pekmez. It is seen that there is high bioavailable iron (Fe{sup 2+}) in pekmez. The developed method is sensitive, simple and need the shorter time in comparison with other similar studies.

  11. Supercritical CO2 extraction of Schinus molle L with co-solvents: mathematical modeling and antimicrobial applications

    OpenAIRE

    Rodrigo Scopel; Roberto Góes Neto; Manuel Alves Falcão; Eduardo Cassel; Rubem Mário Figueiró Vargas

    2013-01-01

    This work investigates the antimicrobial activity of the Schinus molle L. leaves extracts obtained under supercritical conditions using carbon dioxide and co-solvents. Antimicrobial qualitative evaluation was carried out through the bioautography technique and the microorganisms studied were Staphylococcus aureus, Pseudomonas aeruginosas, Escherichia coli, Micrococcus luteus, and Salmonella choleraesuis. The supercritical fluid extraction was carried out in a pilot scale equipment using carbo...

  12. Towards green analysis of virgin olive oil phenolic compounds: Extraction by a natural deep eutectic solvent and direct spectrophotometric detection.

    Science.gov (United States)

    Paradiso, Vito Michele; Clemente, Antonia; Summo, Carmine; Pasqualone, Antonella; Caponio, Francesco

    2016-12-01

    The determination of phenolic compounds in extra virgin olive oils (EVOO) by means of rapid, low-cost, environment-free methods would be a desirable achievement. A natural deep eutectic solvent (DES) based on glucose and lactic acid was considered as extraction solvent for phenolic compounds in EVOO. DESs are green solvents characterized by high availability, biodegradability, safety, and low cost. The spectrophotometric characteristics of DES extracts of 65 EVOO samples were related to the total phenolic content of the oils, assessed by methanol-water extraction coupled to the Folin-Ciocalteu assay. A regression model (ncalibration=45, nvalidation=20), including the absorbance at two wavelengths (257, 324nm), was obtained, with an adjusted R(2)=0.762. Therefore the DES could provide a promising and viable approach for a green screening method of phenolic compounds in EVOO, by means of simple spectrophotometric measurements of extracts, even for on-field analysis (for example in olive mills).

  13. A high-throughput platform for low-volume high-temperature/pressure sealed vessel solvent extractions

    Energy Technology Data Exchange (ETDEWEB)

    Damm, Markus [Christian Doppler Laboratory for Microwave Chemistry (CDLMC) and Institute of Chemistry, Karl-Franzens-University Graz, Heinrichstrasse 28, A-8010 Graz (Austria); Kappe, C. Oliver, E-mail: oliver.kappe@uni-graz.at [Christian Doppler Laboratory for Microwave Chemistry (CDLMC) and Institute of Chemistry, Karl-Franzens-University Graz, Heinrichstrasse 28, A-8010 Graz (Austria)

    2011-11-30

    Highlights: Black-Right-Pointing-Pointer Parallel low-volume coffee extractions in sealed-vessel HPLC/GC vials. Black-Right-Pointing-Pointer Extractions are performed at high temperatures and pressures (200 Degree-Sign C/20 bar). Black-Right-Pointing-Pointer Rapid caffeine determination from the liquid phase. Black-Right-Pointing-Pointer Headspace analysis of volatiles using solid-phase microextraction (SPME). - Abstract: A high-throughput platform for performing parallel solvent extractions in sealed HPLC/GC vials inside a microwave reactor is described. The system consist of a strongly microwave-absorbing silicon carbide plate with 20 cylindrical wells of appropriate dimensions to be fitted with standard HPLC/GC autosampler vials serving as extraction vessels. Due to the possibility of heating up to four heating platforms simultaneously (80 vials), efficient parallel analytical-scale solvent extractions can be performed using volumes of 0.5-1.5 mL at a maximum temperature/pressure limit of 200 Degree-Sign C/20 bar. Since the extraction and subsequent analysis by either gas chromatography or liquid chromatography coupled with mass detection (GC-MS or LC-MS) is performed directly from the autosampler vial, errors caused by sample transfer can be minimized. The platform was evaluated for the extraction and quantification of caffeine from commercial coffee powders assessing different solvent types, extraction temperatures and times. For example, 141 {+-} 11 {mu}g caffeine (5 mg coffee powder) were extracted during a single extraction cycle using methanol as extraction solvent, whereas only 90 {+-} 11 were obtained performing the extraction in methylene chloride, applying the same reaction conditions (90 Degree-Sign C, 10 min). In multiple extraction experiments a total of {approx}150 {mu}g caffeine was extracted from 5 mg commercial coffee powder. In addition to the quantitative caffeine determination, a comparative qualitative analysis of the liquid phase coffee

  14. Solvent-free microwave extraction of essential oil from Dryopteris fragrans and evaluation of antioxidant activity.

    Science.gov (United States)

    Li, Xiao-Juan; Wang, Wei; Luo, Meng; Li, Chun-Ying; Zu, Yuan-Gang; Mu, Pan-Song; Fu, Yu-Jie

    2012-07-15

    Solvent-free microwave extraction (SFME) of the essential oil from Dryopteris fragrans and its antioxidant activity were investigated. A central composite design combined with response surface methodology was applied to study the influences of extraction time, irradiation power and humidity (proportion of water pretreatment). A maximal extraction yield of 0.33% was achieved under optimal conditions of extraction time 34 min, irradiation power 520 W and humidity 51%. Sixteen compounds, representing 89.65% of the oil, were identified, of which the major ones, (1R,4S,11R)-4,6,6,11-tetramethyltricyclo[5.4.0.0(4,8)]undecan-1-ol (30.49%), 1R,4S,7S,11R-2,2,4,8-tetramethyltricyclo[5.3.1.0(4,11)]undec-8-ene (22.91%) and, 1,4,4a,5,6,7,8,8a-octahydro-2,5,5,8a-tetramethyl-1-naphthalenemethanol (15.11%), accounted for 68.51% of the oil. The antioxidant activity of the essential oil was assessed by 2,2-diphenyl-1-picrylhydrazyl (DPPH), β-carotene/linoleic acid, and reducing power assay, the IC50 values were 0.19, 0.09 and 0.18 mg/mL, respectively. All these results suggest that SFME represents an excellent alternative protocol for production of essential oils from plant materials.

  15. Extraction of phenolic compounds from extra virgin olive oil by a natural deep eutectic solvent: Data on UV absorption of the extracts.

    Science.gov (United States)

    Paradiso, Vito Michele; Clemente, Antonia; Summo, Carmine; Pasqualone, Antonella; Caponio, Francesco

    2016-09-01

    This data article refers to the paper "Towards green analysis of virgin olive oil phenolic compounds: extraction by a natural deep eutectic solvent and direct spectrophotometric detection" [1]. A deep eutectic solvent (DES) based on lactic acid and glucose was used as green solvent for phenolic compounds. Eight standard phenolic compounds were solubilized in the DES. Then, a set of extra virgin olive oil (EVOO) samples (n=65) were submitted to liquid-liquid extraction by the DES. The standard solutions and the extracts were analyzed by UV spectrophotometry. This article reports the spectral data of both the standard solutions and the 65 extracts, as well as the total phenolic content of the corresponding oils, assessed by the Folin-Ciocalteu assay.

  16. Impact of quality parameters on the recovery of putrescine and cadaverine in fish using methanol-hydrochloric acid solvent extraction.

    Science.gov (United States)

    Richard, Nicole L; Pivarnik, Lori F; Ellis, P Christopher; Lee, Chong M

    2011-01-01

    Methanol (MeOH) extraction by AOAC Official Method 996.07 has resulted in low amine recoveries in fresh fish tissue. Addition of 25% 0.4 M HCl to the 75% methanol-water extraction solvent resulted in higher recoveries of putrescine and cadaverine. Average putrescine recovery increased from 55 to 92% in flounder, scup, bluefish, and salmon; from 92 to 98% in mackerel; and from 83 to 107% in processed mackerel. Average cadaverine recovery increased from 57 to 95% in flounder, scup, bluefish, and salmon; from 91 to 97% in mackerel; and from 92 to 108% in processed mackerel. Fish stored on ice for 12 days also showed differences between background concentrations determined with the two solvents. However, the values decreased with storage time, indicating that degradation of the protein matrix may cause more comparable measurements between the two solvents. However, consistently higher putrescine and cadaverine measurements were determined using MeOH-HCl. Although significant differences in the extraction of amines from the high-fat fish tissue were not seen between MeOH and MeOH-HCl, it would be ideal to have one solvent for biogenic amine extraction. This study confirms that MeOH-HCl is a better solvent for complete extraction and recovery of putrescine and cadaverine in fresh and processed fish tissues.

  17. "Solvent-free" ultrasound-assisted extraction of lipids from fresh microalgae cells: a green, clean and scalable process.

    Science.gov (United States)

    Adam, Fanny; Abert-Vian, Maryline; Peltier, Gilles; Chemat, Farid

    2012-06-01

    In order to comply with criteria of green chemistry concepts and sustainability, a new procedure has been performed for solvent-free ultrasound-assisted extraction (UAE) to extract lipids from fresh Nannochloropsis oculata biomass. Through response surface methodology (RSM) parameters affecting the oil recovery were optimized. Optimum conditions for oil extraction were estimated as follows: (i) 1000 W ultrasonic power, (ii) 30 min extraction time and (iii) biomass dry weight content at 5%. Yields were calculated by the total fatty acids methyl esters amounts analyzed by GC-FID-MS. The maximum oil recovery was around 0.21%. This value was compared with the one obtained with the conventional extraction method (Bligh and Dyer). Furthermore, effect of temperature on the yield was also investigated. The overall results show an innovative and effective extraction method adapted for microalgae oil recovery, without using solvent and with an enable scaling up. Copyright © 2012 Elsevier Ltd. All rights reserved.

  18. Separation of baicalein from baicalin by means of solvent extraction; Yobai chushutsuho ni yoru baicalein /baicalin no bunri

    Energy Technology Data Exchange (ETDEWEB)

    Kitazaki, H.; Ishimaru, M. [Tsumura and Co., Ibaraki (Japan); Inoue, K.; Yoshida, K. [Saga University, Saga (Japan)

    1996-03-10

    In this work, solvent extraction behaviors of some commercial extractants such as tri-n-octylphosphine oxide (TOPO), Cyanex 923 and Cyanex 925 for baicalein and baicalin decocted from Suctellaria root, which is a crude drug, were examined to elucidate their mutual separation by solvent extraction. Baicalein was extracted selectively by trialkylphosphine oxides over baicalin. From analyses of the extraction mechanism the equilibrium constant of extraction reaction and enthalpy change were evaluated. A porous resin impregnated with Cyanex 923 in XAD-7 was prepared to remove baicalein from baicalin by using a column packed with the resin. Baicalein was able to be completely removed by this column operation. 10 refs., 11 figs., 1 tab.

  19. Deep Eutectic Solvent-Based Microwave-Assisted Method for Extraction of Hydrophilic and Hydrophobic Components from Radix Salviae miltiorrhizae

    Directory of Open Access Journals (Sweden)

    Jue Chen

    2016-10-01

    Full Text Available Deep eutectic solvents (DESs have attracted significant attention as a promising green media. In this work, twenty-five kinds of benign choline chloride-based DESs with microwave-assisted methods were applied to quickly extract active components from Radix Salviae miltiorrhizae. The extraction factors, including temperature, time, power of microwave, and solid/liquid ratio, were investigated systematically by response surface methodology. The hydrophilic and hydrophobic ingredients were extracted simultaneously under the optimized conditions: 20 vol% of water in choline chloride/1,2-propanediol (1:1, molar ratio as solvent, microwave power of 800 W, temperature at 70 °C, time at 11.11 min, and solid/liquid ratio of 0.007 g·mL−1. The extraction yield was comparable to, or even better than, conventional methods with organic solvents. The microstructure alteration of samples before and after extraction was also investigated. The method validation was tested as the linearity of analytes (r2 > 0.9997 over two orders of magnitude, precision (intra-day relative standard deviation (RSD < 2.49 and inter-day RSD < 2.96, and accuracy (recoveries ranging from 95.04% to 99.93%. The proposed DESs combined with the microwave-assisted method provided a prominent advantage for fast and efficient extraction of active components, and DESs could be extended as solvents to extract and analyze complex environmental and pharmaceutical samples.

  20. Ternary diagram of extract proteins / solvent systems: Sesame, soybean and lupine proteins

    Directory of Open Access Journals (Sweden)

    Mohamed, S. S.

    2004-09-01

    Full Text Available Solvent extraction as a method of extracting protein from oilseed meals offers the advantage of higher efficiency. Unfortunately, the published literature points to the gap in the work concerned with the necessary equilibrium diagram to design due process equipment for such extracts. Initiated by this lack of basic knowledge, the present study has been undertaken to provide the equilibrium data for three different ternary systems, namely: sesame protein / sodium hydroxide solution system, soybean protein / sodium hydroxide solution system and lupine protein / sodium hydroxide solution system. These oilseed meals were selected because of their high protein content (53.4 %, 46.2 % and 42.3 % protein, respectively. The study also concentrated on the evaluation of the major parameters affecting the extraction process, i.e. the normality of the sodium hydroxide solution used as extracting solvent and the initial oilseed solvent to meal feeding ratio. The results obtained indicate that the best normality of sodium hydroxide solution used for extracting soybean and lupine protein is 0.02N, while 0.04N solution is required for extracting sesame protein. Also, operating at a liquid to solid feed ratio of 30:1 and 50:1 for soybean, sesame and lupine, respectively, is enough to reach a high protein extract. Correlations were presented for each locus of under flow compositions, graphically acquired, and the data are compared with those calculated by analytical solutions.La extracción con disolventes es un método de extracción de proteínas de las harinas de semillas oleaginosas que ofrece la ventaja de su elevada eficacia. Desafortunadamente, la bibliografía coincide en el vacío existente con respecto a los diagramas de equilibrio necesarios para el diseño de los equipos adecuados. Debido a esta falta de conocimientos, el presente estudio se ha llevado a cabo para obtener datos de tres sistemas ternarios: sistema proteína de sésamo / disolución de

  1. Application of 2k Full Factorial Design in Optimization of Solvent-Free Microwave Extraction of Ginger Essential Oil

    OpenAIRE

    Mumtaj Shah; S K Garg

    2014-01-01

    The solvent-free microwave extraction of essential oil from ginger was optimized using a 23 full factorial design in terms of oil yield to determine the optimum extraction conditions. Sixteen experiments were carried out with three varying parameters, extraction time, microwave power, and type of sample for two levels of each. A first order regression equation best fits the experimental data. The predicted values calculated by the regression model were in good agreement with the experimental ...

  2. Antibacterial activity of sequentially extracted organic solvent extracts of fruits,flowers and leaves of Lawsonia inermis L.from Jaffna

    Institute of Scientific and Technical Information of China (English)

    E; Christy; Jeyaseelan; S; Jenothiny; MK; Pathmanathan; JP; Jeyadevan

    2012-01-01

    Objective:To reveal the antibacterial activity of sequentially extracted different cold organic solvent extracts of fruits,flowers and leaves of Lawsonia inermis(L against)some pathogenic bacteria.Methods:Powders of fruits,flowers and leaves of L inermis were continuously extracted with dichloromethane(DCM),ethyl acetate and ethanol at ambient temperature.The dried extracts were prepared into different concentrations and tested for antibacterial activity by agar well diffusion method,and also the extracts were tested to detennine the available phytochemicals.Results:Except DCM extract of flower all other test extracts revealed inhibitory effect on all tested bacteria and their inhibitory effect differed significantly(P<0.05).The highest inhibitory effect was showed by ethyl acetate extract of flower against Staphylococcus aureus(S.aureus)and Pseudomonas aeruginosa(P.aeruginosa),and ethyl acetate extract of fruit on Escherichia coli(E.coli)and Bacillus subtilis(6.subtilis).The ethyl acetate and ethanol extracts of flower,fruit and leaf expressed inhibition even at 1 mg/100μl against all test bacteria.Among the tested phytochemicals flavonoids were detected in all test extracts except DCM extract of flower.Conclusions:The study demonstrated that the ethyl acetate and ethanol extracts of fruit and flower of L inermis are potentially better source of antibacterial agents compared to leaf extracts of respective solvents.

  3. Vegetable Oils as Alternative Solvents for Green Oleo-Extraction, Purification and Formulation of Food and Natural Products.

    Science.gov (United States)

    Yara-Varón, Edinson; Li, Ying; Balcells, Mercè; Canela-Garayoa, Ramon; Fabiano-Tixier, Anne-Sylvie; Chemat, Farid

    2017-09-05

    Since solvents of petroleum origin are now strictly regulated worldwide, there is a growing demand for using greener, bio-based and renewable solvents for extraction, purification and formulation of natural and food products. The ideal alternative solvents are non-volatile organic compounds (VOCs) that have high dissolving power and flash point, together with low toxicity and less environmental impact. They should be obtained from renewable resources at a reasonable price and be easy to recycle. Based on the principles of Green Chemistry and Green Engineering, vegetable oils could become an ideal alternative solvent to extract compounds for purification, enrichment, or even pollution remediation. This review presents an overview of vegetable oils as solvents enriched with various bioactive compounds from natural resources, as well as the relationship between dissolving power of non-polar and polar bioactive components with the function of fatty acids and/or lipid classes in vegetable oils, and other minor components. A focus on simulation of solvent-solute interactions and a discussion of polar paradox theory propose a mechanism explaining the phenomena of dissolving polar and non-polar bioactive components in vegetable oils as green solvents with variable polarity.

  4. Electron Acceleration In Impulsive Solar Flares : extract of a thesis

    CERN Document Server

    Lenters, G T

    1999-01-01

    Impulsive solar flares generate a wide range of photon and particle emissions and hence provide an excellent backyard laboratory for studying particle acceleration processes in astrophysical plasmas. The source of the acceleration remains unidentified, but the basic observations are clear: (1) Hard X-ray and gamma-ray line emission occur simultaneously, indicating that electron and ion acceleration must occur simultaneously; (2) the electron and ion precipitation rates at the foot-points of the flare must be extremely large to account for the photon emission (∼1037 electrons s −1 and ∼1035 protons s−1, respectively), which means that replenishment of the acceleration region (which contains ≈1037 fully ionized hydrogen atoms) is a crucial issue; and (3) there are enhancements of the heavy ion abundances relative to normal coronal values. The basic model proposed assumes the generation of extremely low levels of magnetohydrodynamic (MHD) turb...

  5. Effect of different solvents extracts and mode of action of Loktanella spp. Gb03 on toxic dinoflagellate

    Science.gov (United States)

    Hameed, Anmar; Usup, Gires; Ahmad, Asmat

    2016-11-01

    This study was aimed to evaluate the algicidal activity of Loktanella sp. Gb-03 bacterial extracts against toxic dinoflagellate, using various polar and non-polar solvents. For this purpose, six different solvent extracts were prepared (i.e. methanol, ethyl acetate, hexane, chloroform, acetonitrile and water). Ratio of 1:100 (v:v) (extract to dinoflagellate culture) of each extract was used for preliminary algicidal activity screening against toxic dinoflagellate Coolia malaynesis. Dinoflagellate cells at the stationary phase (1.0 × 103 cells/ mL) were treated with 1% (v/v) of each extract by using 24-well microplate. The plates were then incubated for 24 hours at dinoflagellate culture condition (under a light intensity of 140 µmol m-2s-1 and 12:12 hours light:dark photoperiod). The result of algicidal activity screening showed that all 6 extracts from Loktanella sp. Gb-03 had different ranges of algicidal activity against the toxic dinoflagellates. Ethyl acetate extract showed the highest activity against C. malaynesis and also other harmful dinoflagellate (Alexandrium sp. Alexandrium leei, Alexandrium affine, Alexandrium tamiyavanichi, Alexandrium tamarense, Gambierdiscus belizeanus, and Ostreopsis). This study was the first to explore the algicidal activity of Loktanella sp. Gb-03 extracts against toxic dinoflagellate with ethyl acetate as the best solvent to extract algicidal active compounds.

  6. Enhanced and green extraction polyphenols and furanocoumarins from Fig (Ficus carica L.) leaves using deep eutectic solvents.

    Science.gov (United States)

    Wang, Tong; Jiao, Jiao; Gai, Qing-Yan; Wang, Peng; Guo, Na; Niu, Li-Li; Fu, Yu-Jie

    2017-10-25

    Nowadays, green extraction of bioactive compounds from medicinal plants has gained increasing attention. As green solvent, deep eutectic solvent (DES) have been highly rated to replace toxic organic solvents in extraction process. In present study, to simultaneous extraction five main bioactive compounds from fig leaves, DES was tailor-made. The tailor-made DES composed of a 3:3:3 molar ratio of glycerol, xylitol and D-(-)-Fructose showed enhanced extraction yields for five target compounds simultaneously compared with traditional methanol and non-tailor DESs. Then, the tailor-made DES based extraction methods have compared and microwave-assisted extraction was selected and optimized due to its high extraction yields with lower time consumption. The influencing parameters including extraction temperature, liquid-solid ratio, and extraction time were optimized using response surface methodology (RSM). Under optimal conditions the extraction yield of caffeoylmalic acid, psoralic acid-glucoside, rutin, psoralen and bergapten was 6.482mg/g, 16.34mg/g, 5.207mg/g, 15.22mg/g and 2.475mg/g, respectively. Macroporous resin D101 has been used to recovery target compounds with recovery yields of 79.2%, 83.4%, 85.5%, 81.2% and 75.3% for caffeoylmalic acid, psoralic acid-glucoside, rutin, psoralen and bergapten, respectively. The present study suggests that DESs are truly designer and efficient solvents and the method we developed was efficient and sustainable for extraction main compounds from Fig leaves.mg/g. Copyright © 2017 Elsevier B.V. All rights reserved.

  7. Solvent extraction separation of copper and zinc from MSWI fly ash leachates.

    Science.gov (United States)

    Tang, Jinfeng; Steenari, Britt-Marie

    2015-10-01

    Fly ash from combustion of municipal solid waste (MSW) contains significant amounts of metals, some of which are valuable and some of which are potentially toxic. This type of ash is most often stabilized and landfilled which means that the metals will be difficult to reclaim at a later stage. In recent years efforts have been made to develop feasible methods to recover selected metals, such as Zn, from MSW fly ash. If this would be possible, a significant amount of valuable metals could be re-inserted in the industrial material loops. This paper describes the development and evaluation of a process for recovery of Cu and Zn from MSW combustion fly ash based on hydrochloric acid leaching followed by two solvent extraction processes, one for each metal. The separation of Cu from the acid leachate was done using an aldoxime extractant, LIX860N-I, in kerosene and a mixture of phosphine oxides, Cyanex 923, also in kerosene, was used for extraction of Zn from the Cu-depleted aqueous phase. The extraction of Cu was selective, but a significant amount of other metals, such as Fe and Pb, were co-extracted together with Zn. It was shown that it is possible to decrease the contamination of Fe by using a suitable concentration of nitric acid solution for stripping or by removing the contaminating metals through cementation. The suggested process was tested for two MSW combustion fly ashes in laboratory scale experiments and gave Cu yields of 69-87% and Zn yields of 75-80% based on the contents in the ash.

  8. A solvent-extraction module for cyclotron production of high-purity technetium-99m.

    Science.gov (United States)

    Martini, Petra; Boschi, Alessandra; Cicoria, Gianfranco; Uccelli, Licia; Pasquali, Micòl; Duatti, Adriano; Pupillo, Gaia; Marengo, Mario; Loriggiola, Massimo; Esposito, Juan

    2016-12-01

    The design and fabrication of a fully-automated, remotely controlled module for the extraction and purification of technetium-99m (Tc-99m), produced by proton bombardment of enriched Mo-100 molybdenum metallic targets in a low-energy medical cyclotron, is here described. After dissolution of the irradiated solid target in hydrogen peroxide, Tc-99m was obtained under the chemical form of (99m)TcO4(-), in high radionuclidic and radiochemical purity, by solvent extraction with methyl ethyl ketone (MEK). The extraction process was accomplished inside a glass column-shaped vial especially designed to allow for an easy automation of the whole procedure. Recovery yields were always >90% of the loaded activity. The final pertechnetate saline solution Na(99m)TcO4, purified using the automated module here described, is within the Pharmacopoeia quality control parameters and is therefore a valid alternative to generator-produced (99m)Tc. The resulting automated module is cost-effective and easily replicable for in-house production of high-purity Tc-99m by cyclotrons.

  9. ENCAPSULATION OF EXTRACT FROM WINERY INDUSTRY RESIDUE USING THE SUPERCRITICAL ANTI-SOLVENT TECHNIQUE

    Directory of Open Access Journals (Sweden)

    N. Mezzomo

    Full Text Available Abstract Grape pomace (seed, skin and stem is a winery byproduct with high levels of biologically active compounds, such as antioxidants and antimicrobials, that could be converted into high added-value products. Since these components are easily degraded by oxygen, light and high temperature exposure, stabilization is important, for instance, by a microencapsulation process. Therefore, the objective of this study was to investigate the influence on the particle characteristics of the operational conditions applied in the Supercritical Anti-Solvent (SAS process for the co-precipitation of grape pomace extract and poly(-lactic-co-glycolic acid (PLGA. The morphology and size of the particles formed, their stability and thermal profile were evaluated, and also the co-precipitation efficiency. The conditions studied allowed the production of microparticles with spherical shape for all operational conditions, with estimated particle size between 4 ± 2 and 11 ± 5 µm, and very good co-precipitation efficiencies (up to 94.4 ± 0.6%. The co-precipitated extract presented higher stability compared to the crude extract, indicating the effectiveness of the co-precipitation process and coating material against degradation processes.

  10. An investigation of influence of solvent on the degradation kinetics of carotenoids in oil extracts of Calendula officinalis

    Directory of Open Access Journals (Sweden)

    DEJAN BEZBRADICA

    2005-02-01

    Full Text Available The stability of carotenoids was studied in marigold oil extracts prepared with following solvents: Myritol 312®, paraffin oil, almond oil, olive oil, sunflower oil, grape seed oil, and soybean oil. The concentration of the carotenoids was determined by spectroscopic measurement at 450 nm. Degradation rate showed a first order dependence on the concentration of carotenoids with a faster first stage (which lasted 35–50 days, depending on the solvent and a slower second stage. The highest degradation rates were observed in extracts prepared with linoleic acid rich solvents (sunflower oil, soybean oil and grape seed oil, while the lowest were found in oil with saturated fatty acids (Myritol 312® and paraffin oil. These results confirm the connection between the degradation of carotenoids and lipid autoxidation, and suggest that the influence of the oil solvents on the stability of oil extracts of Calendula officinalis is a factor that must be considered when selecting a solvent for the production of marigold oil extracts.

  11. Preliminary phytochemical investigation and in vitro anthelmintic activities ofMaesa lanceolata solvent extracts againstLymnatis nilotica (aquatic leech)

    Institute of Scientific and Technical Information of China (English)

    Wondu Dagnaw; Alemayehu Mekonnen

    2016-01-01

    Objective:To investigate phytochemicals constituents and check the anthelmintic activities of Maesa lanceolata (M. lanceolata) solvent extracts against aquatic leech. Methods: Several phytochemicals were tested and screened from petroleum ether, chloroform and methanol extracts ofM. lanceolata extracts and their anthelmintic activities were done based on the standard procedure against aquatic leech. Piperazine citrate (20 mg/mL) was used as a reference standard while distilled water was used as a control. Results:Qualitative phytochemical analysis of different solvent (petroleum ether, chloroform and methanol) extracts ofM. lanceolata revealed the presence of flavonoids and alkaloids in chloroform extracts and alkaloids in methanol extracts. In addition to the qualitative analysis of the plant extracts, the anthelmintic effects were also evaluated against aquatic leech (Lymnatis nilotica). Accordingly, various concentrations (10, 20, 40 and 60 mg/mL) of each solvent (petroleum ether, chloroform and methanol) extracts and 20 mg/mL of standard drug were prepared and tested against the selected leech. All the tested concentrations showed anthelmintic activities in a dose-dependent manner. From petroleum ether, chloroform and methanol extracts, chloroform extracts with 60 mg/mL concentration was effective with the paralytic time of (29.00 ± 1.06) min and death time of (65.00 ± 2.00) min in gradient extraction method. But in the case of extraction without gradient method, methanol extracts with 60 mg/mL concentration showed effective paralysis and death time (26.00 ± 1.73) and (56.00 ± 1.56) min, respectively, against the selected aquatic leech. Conclusions:The present study revealed thatM. lanceolata extracts have magic anthelmintic activities which are helpful to treat aquatic leeches (Lymnatis nilotica) which are associated with the nasal cavities of animals and human beings.

  12. Design of the plasma chamber and beam extraction system for SC ECRIS of RAON accelerator

    Science.gov (United States)

    Kim, Y.; Choi, S.; Hong, I. S.

    2014-02-01

    The RAON accelerator is the heavy ion accelerator being built in Korea. It contains a 3rd generation SC ECRIS which uses 28 GHz/18 GHz microwave power to extract 12 puA uranium ion beams. A plasma chamber for that ECRIS is made of aluminum machined from bulk Al. That chamber contains cooling channels to remove dumped power and another access port for microwave introduction and plasma diagnostics. Beam extraction electrodes were designed considering the engineering issues and preliminary beam extraction analysis was done. That plasma chamber will be assembled with a cryostat, and beam extraction experiment will be done.

  13. LPS-induced NO inhibition and antioxidant activities of ethanol extracts and their solvent partitioned fractions from four brown seaweeds

    Science.gov (United States)

    Cho, Myoung Lae; Lee, Dong-Jin; Lee, Hyi-Seung; Lee, Yeon-Ju; You, Sang Guan

    2013-12-01

    The nitric oxide inhibitory (NOI) and antioxidant (ABTS and DPPH radical scavenging effects with reducing power) activities of the ethanol (EtOH) extracts and solvent partitioned fractions from Scytosiphon lomentaria, Chorda filum, Agarum cribrosum, and Desmarestia viridis were investigated, and the correlation between biological activity and total phenolic (TP) and phlorotannin (TPT) content was determined by PCA analysis. The yield of EtOH extracts from four brown seaweeds ranged from 2.6 to 6.6% with the highest yield from D. viridis, and the predominant compounds in their solvent partitioned fractions had medium and/or less polarity. The TP and TPT content of the EtOH extracts were in the ranges of 25.0-44.1 mg GAE/g sample and 0.2-4.6 mg PG/g sample, respectively, which were mostly included in the organic solvent partitioned fractions. Strong NOI activity was observed in the EtOH extracts and their solvent partitioned fractions from D. viridis and C. filum. In addition, the EtOH extract and its solvent partitioned fractions of D. viridis exhibited little cytotoxicity to Raw 264.7 cells. The most potent ABTS and DPPH radical scavenging capacity was shown in the EtOH extracts and their solvent partitioned fractions from S. lomentaria and C. filum, and both also exhibited strong reducing ability. In the PCA analysis the content of TPT had a good correlation with DPPH ( r = 0.62), ABTS ( r = 0.69) and reducing power ( r = 0.65), however, an unfair correlation was observed between the contents of TP and TPT and NOI, suggesting that the phlorotannins might be responsible for the DPPH and ABTS radical scavenging activities.

  14. Effects of extraction solvent mixtures on antioxidant activity evaluation and their extraction capacity and selectivity for free phenolic compounds in barley (Hordeum vulgare L.).

    Science.gov (United States)

    Zhao, Haifeng; Dong, Jianjun; Lu, Jian; Chen, Jian; Li, Yin; Shan, Lianju; Lin, Yan; Fan, Wei; Gu, Guoxian

    2006-09-20

    Four kinds of solvent extracts from three Chinese barley varieties (Ken-3, KA4B, and Gan-3) were used to examine the effects of extraction solvent mixtures on antioxidant activity evaluation and their extraction capacity and selectivity for free phenolic compounds in barley through free radical scavenging activity, reducing power and metal chelating activity, and individual and total phenolic contents. Results showed that extraction solvent mixtures had significant impacts on antioxidant activity estimation, as well as different extraction capacity and selectivity for free phenolic compounds in barley. The highest DPPH* and ABTS*+ scavenging activities and reducing power were found in 80% acetone extracts, whereas the strongest *OH scavenging activity, O2*- scavenging activity, and metal chelating activity were found in 80% ethanol, 80% methanol, and water extracts, respectively. Additionally, 80% acetone showed the highest extraction capacity for (+)-catechin and ferulic, caffeic, vanillic, and p-coumaric acids, 80% methanol for (-)-epicatechin and syringic acid, and water for protocatechuic and gallic acids. Furthermore, correlations analysis revealed that TPC, reducing power, DPPH* and ABTS*+ scavenging activities were well positively correlated with each other (p antioxidant activity, 80% acetone was recommended to extract free phenolic compounds from barley. DPPH* scavenging activity and ABTS*+ scavenging activity or reducing power could be used to assess barley antioxidant activity.

  15. Identical extraction behavior and coordination of trivalent or hexavalent f-element cations using ionic liquid and molecular solvents.

    Science.gov (United States)

    Cocalia, Violina A; Jensen, Mark P; Holbrey, John D; Spear, Scott K; Stepinski, Dominique C; Rogers, Robin D

    2005-06-07

    The extraction of both UO2(2+) and trivalent lanthanide and actinide ions (Am3+, Nd3+, Eu3+) by dialkylphosphoric or dialkylphosphinic acids from aqueous solutions into the ionic liquid, 1-decyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide has been studied and compared to extractions into dodecane. Radiotracer partitioning measurements show comparable patterns of distribution ratios for both the ionic liquid/aqueous and dodecane/aqueous systems, and the limiting slopes at low acidity indicate the partitioning of neutral complexes in both solvent systems. The metal ion coordination environment, elucidated from EXAFS and UV-visible spectroscopy measurements, is equivalent in the ionic liquid and dodecane solutions with coordination of the uranyl cation by two hydrogen-bonded extractant dimers, and of the trivalent cations by three extractant dimers. This is the first definitive report of a system where both the biphasic extraction equilibria and metal coordination environment are the same in an ionic liquid and a molecular organic solvent.

  16. DEVELOPMENT OF CONTINUOUS SOLVENT EXTRACTION PROCESSES FOR COAL DERIVED CARBON PRODUCTS

    Energy Technology Data Exchange (ETDEWEB)

    Elliot B. Kennel; Chong Chen; Dady Dadyburjor; Liviu Magean; Peter G. Stansberry; Alfred H. Stiller; John W. Zondlo

    2005-07-13

    The purpose of this DOE-funded effort is to develop continuous processes for solvent extraction of coal for the production of carbon products. These carbon products include materials used in metals smelting, especially in the aluminum and steel industries, as well as porous carbon structural material referred to as ''carbon foam'' and carbon fibers. The Hydrotreatment Facility is being prepared for trials with coal liquids. Raw coal tar distillate trials have been carried out by heating coal tar in the holding tank in the Hydrotreatment Facility. The liquids are centrifuged to warm the system up in preparation for the coal liquids. The coal tar distillate is then recycled to keep the centrifuge hot. In this way, the product has been distilled such that a softening point of approximately 110 C is reached. Then an ash test is conducted.

  17. Hybrid Perovskite Quantum Nanostructures Synthesized by Electrospray Antisolvent-Solvent Extraction and Intercalation.

    Science.gov (United States)

    Naphade, Rounak; Nagane, Satyawan; Shanker, G Shiva; Fernandes, Rohan; Kothari, Dushyant; Zhou, Yuanyuan; Padture, Nitin P; Ogale, Satishchandra

    2016-01-13

    Perovskites based on organometal lead halides have attracted great deal of scientific attention recently in the context of solar cells and optoelectronic devices due to their unique and tunable electronic and optical properties. Herein, we show that the use of electrospray technique in conjunction with the antisolvent-solvent extraction leads to novel low-dimensional quantum structures (especially 2-D nanosheets) of CH3NH3PbI3- and CH3NH3PbBr3-based layered perovskites with unusual luminescence properties. We also show that the optical bandgaps and emission characteristics of these colloidal nanomaterials can be tuned over a broad range of visible spectral region by compositional tailoring of mixed-halide (I- and Br-based) perovskites.

  18. Controllability of plutonium concentration for FBR fuel at a solvent extraction process in the PUREX process

    Energy Technology Data Exchange (ETDEWEB)

    Enokida, Youichi; Kitano, Motoki; Sawada, Kayo [Nagoya University, 1 Furo-cho, Chikusa-ku, Nagoya-shi, Aichi-ken, 4630052 (Japan)

    2013-07-01

    Typical Purex solvent extraction systems for the reprocessing of spent nuclear fuel have a feed material containing dilute, 1% in weight, plutonium, along with uranium and fission products. Current reprocessing proposals call for no separation of the pure plutonium. The work described in this paper studied, by computer simulation, the fundamental feasibility of preparing a 20% concentrated plutonium product solution from the 1% feed by adjusting only the feed rates and acid concentrations of the incoming streams and without the addition of redox reagents for the plutonium. A set of process design flowsheets has been developed to realize a concentrated plutonium solution of a 20% stream from the dilute plutonium feed without using redox reagents. (authors)

  19. Solvent extraction equipment evaluation study. Part 1. Review of the literature

    Energy Technology Data Exchange (ETDEWEB)

    Geier, R.G.; Browne, L.M. (comps.)

    1977-01-01

    This is Part 1 of a three-part document that reviews the solvent extraction contactors available for use in radiochemical reprocessing plants. The three parts are: Part 1: A Review of the Literature, Part 2: Workshop Proceedings, Part 3: A Summary. The main objective of the document is to provide an information base to aid in contactor selection and design of future reprocessing plants. The Literature Review (Part 1) brings together scattered data on all major contactors in use today. It contains an annotated bibliography of the citations used in the review and a complete listing of all the citations screened prior to the review. These bibliographies should aid in determining which reports would be most useful if additional information is desired.

  20. The structures of CyMe4-BTBP complexes of americium(iii) and europium(iii) in solvents used in solvent extraction, explaining their separation properties.

    Science.gov (United States)

    Ekberg, Christian; Löfström-Engdahl, Elin; Aneheim, Emma; Foreman, Mark R StJ; Geist, Andreas; Lundberg, Daniel; Denecke, Melissa; Persson, Ingmar

    2015-11-14

    Separation of trivalent actinoid (An(iii)) and lanthanoid (Ln(iii)) ions is extremely challenging due to their similar ionic radii and chemical properties. Poly-aromatic nitrogen compounds acting as tetradentate chelating ligands to the metal ions in the extraction, have the ability to sufficiently separate An(iii) from Ln(iii). One of these compounds, 6,6'-bis(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-benzol[1,2,4]triazin-3-yl)[2,2]bipyridine, CyMe4-BTBP, has proven to be resistant towards acidic environments and strong radiation from radioactive decomposition. EXAFS studies of the dicomplexes of CyMe4-BTBP with americium(iii) and europium(iii) in nitrobenzene, cyclohexanone, 1-hexanol, 1-octanol and malonamide (DMDOHEMA) in 1-octanol have been carried out to get a deeper understanding of the parameters responsible for the separation. The predominating complexes independent of solvent used are [Am(CyMe4-BTBP)2(NO3)](2+) and [Eu(CyMe4-BTBP)2](3+), respectively, which are present as outer-sphere ion-pairs with nitrate ions in the studied solvents with low relative permittivity. The presence of a nitrate ion in the first coordination sphere of the americium(iii) complex compensates the charge density of the complex considerably in comparison when only outer-sphere ion-pairs are formed as for the [Eu(CyMe4-BTBP)2](3+) complex. The stability and solubility of a complex in a solvent with low relative permittivity increase with decreasing charge density. The [Am(CyMe4-BTBP)2(NO3)](2+) complex will therefore be increasingly soluble and stabilized over the [Eu(CyMe4-BTBP)2](3+) complex in solvents with decreasing relative permittivity of the solvent. The separation of americium(iii) from europium(iii) with CyMe4-BTBP as extraction agent will increase with decreasing relative permittivity of the solvent, and thereby also with decreasing solubility of CyMe4-BTBP. The choice of solvent is therefore a balance of a high separation factor and sufficient solubility of the CyMe4-BTBP

  1. Speciation of arsenic using chelation solvent extraction and high performance liquid chromatography

    Energy Technology Data Exchange (ETDEWEB)

    Cathum, Shamil J.; Obenauf, Alison; Punt, Monique [SAIC Canada, Ottawa, Ontario (Canada); Brown, Carl E. [Emergencies Engineering Technology Office, Environmental Technology Centre, Environment Canada, Ottawa, Ontario (Canada)

    2007-02-15

    Research interest in speciation of arsenic stems from its species dependent behavior in the environment and in living organisms. The complexity of the matrix to be analyzed and low concentrations of target arsenic species that may be labile or difficult to chromatogram, indicate that a suitable pre-treatment methodology is required. This study investigated the usefulness of chelation solvent extraction - high performance liquid chromatography (CSE-HPLC) for the speciation of arsenic in water. It involved reacting arsenic with the chelant known for its affinity towards arsenic, followed by extraction, separation, and identification of the arsenic-chelant-arsenic complex. Arsenic species having different physicochemical properties were investigated. Species, such as, As{sub 2}O{sub 3}, As{sub 3}O{sub 5}, KH{sub 2}AsO{sub 4}, Na{sub 2}HAsO{sub 4}, and NaAsO{sub 2}were detected as a group of closely eluted peaks with different retention times and spectral properties, whereas, the organic arsenic species CH {sub 3}Na {sub 2}AsO {sub 3}, o-arsanilic acid, roxarson and triphenyl arsine separated quite well on the EnviroseP-CM HPLC column. Key method parameters, such as, type of HPLC column, composition of mobile phase and organic solvents affecting peak resolution and sensitivity were optimized. Real environmental matrices contaminated with arsenic were analyzed under varying wavelengths ({lambda}{sub max} = 190, 210, 220, 234, 244, and 282 nm), with good precision. Different arsenic species were detected in these samples with excellent background and signal-to-noise ratios demonstrating the robustness of the method. The detection limit, reproducibility, selectivity, accuracy, and dynamic range of the calibration curves were evaluated. (Abstract Copyright [2007], Wiley Periodicals, Inc.)

  2. Solvent and extraction methods effects on the quality of eel (Anguilla bicolor) oil

    Science.gov (United States)

    Sasongko, H.; Efendi, N. R.; Budihardjo, A.; Farida, Y.; Amartiwi, T.; Rahmawati, A. A.; Wicaksono, A.; Sugiyarto

    2017-01-01

    Eel (Anguilla bicolor) is a general fish consumption in many countries, especially Japan, China, Germany, and France. Besides its vitamin rich, eel oil is also known to contain fatty acids that are necessary for pharmaceutical purposes and as food a supplement. This research was aimed to evaluate the quality of eel oil by different solvent and extraction methods. In this study, fresh eels were extracted using maceration and reflux methods.Chloroform was used as the solvent in the maceration while water used in the reflux method. The oil quality was examined based on the Official Methods of Analysis of the Association of Official Analytical Chemist (AOAC).The result showed that the yield of eel oil using maceration method was 5.44% ± 0.64 with a specific gravity of 0.915 g/mL, while reflux method obtained the yield of 5.33 % ± 0.84 and specific gravity of 0.8575 g/mL. The physicochemical parameters of oil quality used in this study were acid, peroxide, saponification, and iodine value. The maceration method obtained the acid value of 17.389 mgKOH/g, the peroxide value of 7.021meqO2/kg, the saponification value of 111.16mgKOH/g, and the iodine value of 65.14 WIJS. While the reflux method produced the acid value of 9.116 mgKOH/g, the peroxide value of 6.088 meqO2/kg, the saponification value of 70 mgKOH/g, and the iodine value of 87.74 WIJS.

  3. Supercritical CO2 extraction of Schinus molle L with co-solvents: mathematical modeling and antimicrobial applications

    Directory of Open Access Journals (Sweden)

    Rodrigo Scopel

    2013-06-01

    Full Text Available This work investigates the antimicrobial activity of the Schinus molle L. leaves extracts obtained under supercritical conditions using carbon dioxide and co-solvents. Antimicrobial qualitative evaluation was carried out through the bioautography technique and the microorganisms studied were Staphylococcus aureus, Pseudomonas aeruginosas, Escherichia coli, Micrococcus luteus, and Salmonella choleraesuis. The supercritical fluid extraction was carried out in a pilot scale equipment using carbon dioxide modified by the addition of co-solvents, such as ethanol and water at 150 bar and 333 K. A mathematical modeling of the process was also performed.

  4. An absorbing microwave micro-solid-phase extraction device used in non-polar solvent microwave-assisted extraction for the determination of organophosphorus pesticides

    Energy Technology Data Exchange (ETDEWEB)

    Wang Ziming, E-mail: wangziming@jlu.edu.cn [College of Chemistry, Jilin University, 2699 Qianjin Street, Changchun 130012 (China); College of Environment and Resources, Jilin University, 2699 Qianjin Street, Changchun 130012 (China); Zhao Xin; Xu Xu; Wu Lijie; Su Rui; Zhao Yajing; Jiang Chengfei; Zhang Hanqi [College of Chemistry, Jilin University, 2699 Qianjin Street, Changchun 130012 (China); Ma Qiang [Chinese Academy of Inspection and Quarantine, Beijing 100123 (China); Lu Chunmei [College of Technology Center, Jilin Entry-Exit Inspection and Quarantine Bureau, Changchun 130062 (China); Dong Deming [College of Environment and Resources, Jilin University, 2699 Qianjin Street, Changchun 130012 (China)

    2013-01-14

    Highlights: Black-Right-Pointing-Pointer An absorbing microwave {mu}-SPE device packed with activated carbon was used. Black-Right-Pointing-Pointer Absorbing microwave {mu}-SPE device was made and used to enrich the analytes. Black-Right-Pointing-Pointer Absorbing microwave {mu}-SPE device was made and used to heat samples directly. Black-Right-Pointing-Pointer MAE-{mu}-SPE was applied to the extraction of OPPs with non-polar solvent only. - Abstract: A single-step extraction-cleanup method, including microwave-assisted extraction (MAE) and micro-solid-phase extraction ({mu}-SPE), was developed for the extraction of ten organophosphorus pesticides in vegetable and fruit samples. Without adding any polar solvent, only one kind of non-polar solvent (hexane) was used as extraction solvent in the whole extraction step. Absorbing microwave {mu}-SPE device, was prepared by packing activated carbon with microporous polypropylene membrane envelope, and used as not only the sorbent in {mu}-SPE, but also the microwave absorption medium. Some experimental parameters effecting on extraction efficiency was investigated and optimized. 1.0 g of sample, 8 mL of hexane and three absorbing microwave {mu}-SPE devices were added in the microwave extraction vessel, the extraction was carried out under 400 W irradiation power at 60 Degree-Sign C for 10 min. The extracts obtained by MAE-{mu}-SPE were directly analyzed by GC-MS without any clean-up process. The recoveries were in the range of 93.5-104.6%, and the relative standard deviations were lower than 8.7%.

  5. Cytotoxic effects of solvent-extracted active components of Salvia miltiorrhiza Bunge on human cancer cell lines.

    Science.gov (United States)

    Sung, Bokyung; Chung, Hye Sun; Kim, Minjung; Kang, Yong Jung; Kim, Dong Hwan; Hwang, Seong Yeon; Kim, Min Jo; Kim, Cheol Min; Chung, Hae Young; Kim, Nam Deuk

    2015-04-01

    Herbal extracts and dietary supplements may be extracted from the medicinal plants used in traditional Chinese medicine, and are used increasingly commonly worldwide for their benefits to health and quality of life. Thus, ensuring that they are safe for human consumption is a critical issue for the preparation of plant extracts as dietary supplements. The present study investigated extracts of Salvia miltiorrhiza Bunge (S. miltiorrhiza), traditionally used in Asian countries to treat a variety of conditions, as a dietary supplement or as an ingredient in functional foods. Dried S. miltiorrhiza root was extracted with various solvents and under varying extraction conditions, and the effects of the extracts on the viability of five human cancer cell lines were compared. Extracts obtained using 100% ethanol and 100% acetone as solvents exhibited more potent effects compared with extracts obtained using 70 and 30% aqueous ethanol. Furthermore, the active components of S. miltiorrhiza ethanol extracts, known as tanshinones, were investigated. Dihydrotanshinone I was observed to exhibit a higher cytotoxic potential compared with the other tanshinones in the majority of the examined cell lines. Conversely, cryptotanshinone exhibited weak anti-cancer activity. In summary, the results of the present study suggest that the active components obtained from an ethanol extract of S. miltiorrhiza possess the potential to be used as ingredients in functional and health care foods that may be used to improve the effectiveness of chemotherapeutics in the prevention and/or treatment of cancer.

  6. Fast Determination of Essential Oil from Dried Menthol Mint and Orange Peel by Solvent Free Microwave Extraction Using Carbonyl Iron Powder as the Microwave Absorption Medium

    Institute of Scientific and Technical Information of China (English)

    WANG Zi-Ming; DING Lan; WANG Lu; FENG Jin; LI Tie-Chun; ZHOU Xin; ZHANG Han-Qi

    2006-01-01

    An improved solvent free microwave extraction, in which a kind of microwave absorption medium (carbonyl iron powder) was used, was applied to the extraction of essential oil from dried menthol mint and orange peel without addition of any solvent and pretreatment. It took much less time of extraction (30 min) than microwave-assisted hydrodistillation (90 min) and conventional hydrodistillation (180 min). The kinds of chemical compositions in essential oil extracted by different methods were almost the same and such improved solvent free microwave extraction can be a feasible way in extraction of essential oil from dried plant materials.

  7. Thermal And Spectroscopic Analyses Of Next Generation Caustic Side Solvent Extraction Solvent Contacted With 3, 8, And 16 Molar Nitric Acid

    Energy Technology Data Exchange (ETDEWEB)

    Fondeur, F. F.; Fink, S. D.

    2011-12-07

    A new solvent system referred to as Next Generation Solvent or NGS, has been developed at Oak Ridge National Laboratory for the removal of cesium from alkaline solutions in the Caustic Side Solvent Extraction process. The NGS is proposed for deployment at MCU{sup a} and at the Salt Waste Processing Facility. This work investigated the chemical compatibility between NGS and 16 M, 8 M, and 3 M nitric acid from contact that may occur in handling of analytical samples from MCU or, for 3 M acid, which may occur during contactor cleaning operations at MCU. This work shows that reactions occurred between NGS components and the high molarity nitric acid. Reaction rates are much faster in 8 M and 16 M nitric acid than in 3 M nitric acid. In the case of 16 M and 8 M nitric acid, the nitric acid reacts with the extractant to produce initially organo-nitrate species. The reaction also releases soluble fluorinated alcohols such as tetrafluoropropanol. With longer contact time, the modifier reacts to produce a tarry substance with evolved gases (NO{sub x} and possibly CO). Calorimetric analysis of the reaction product mixtures revealed that the organo-nitrates reaction products are not explosive and will not deflagrate.

  8. Quality assessment of Moringa concanensis seed oil extracted through solvent and aqueous-enzymatic techniques

    Directory of Open Access Journals (Sweden)

    Anwar, Farooq

    2008-03-01

    Full Text Available The composition and quality of the M. concanensis seed oil extracted through an aqueous-enzyme-assisted technique, using three commercial enzyme-mixtures (Natuzyme, Kemzyme, and Feedzyme was compared to those of the control-, (without enzymes and solvent-extracted oils. Aqueous enzyme-extracted M.concanensis seed oil content ranged from 23.54 to 27.46% and was significantly (P 0.05 variation in the contents of fiber and ash within the three extraction methods. However, the protein content of the meal obtained through the aqueous-enzyme and control methods was significantly (P M. concanensis seed oils extracted using the three methods. The specific extinctions at 232 and 270 nm, peroxide value, p-anisidine, free fatty acid contents and color values of the aqueous-enzyme-extracted oil were found to be lower than that of solvent-extracted oil and thus revealed good quality. The oils extracted through the three methods exhibited no significant (P En este estudio se compara la composición y la calidad del aceite de semilla de M. concanensis extraído mediante enzimas, utilizando tres enzimas comerciales (Natuzyme, Kemzyme, y Feedzyme con las de un control extraído sin enzimas y con las del aceite extraído con disolvente. El contenido en aceites de las semilla extraídas con enzimas osciló entre 23,54 a 27,46% y fue significativamente más elevado (P 0,05 en el contenido de fibra y ceniza para los tres métodos de la extracción. Sin embargo, el contenido proteínico de la harina obtenido por métodos enzimáticos y el control sin enzimas fue significativamente menor (P < 0,05 que el de la harina obtenida después de la extracción por disolvente. Las diferencias en el índice de yodo (67.1-68.0 g /100 g of oil, densidad en 24 °C (0,865-0,866 g/mL, índice de refracción a 40 °C (1,4622-1,4627 y fracción insaponificable (0,69-0,76 % no fueron significativamente diferentes para ninguna de las técnicas de extracción. Las extinciones espec

  9. Irradiation Effects on Phase-Separation Performance Using a Centrifugal Contactor in a Caustic-Side Solvent Extraction Process

    Energy Technology Data Exchange (ETDEWEB)

    Birdwell, J.F.

    2001-09-12

    A test program has been conducted to determine the extent to which irradiation of a calixarene-based cesium extractant affects-separation of the organic (solvent) phase from aqueous solutions with which it is contacted in a prototype extraction flowsheet. A caustic-side solvent extraction process, known as CSSX, has been developed for the selective removal of cesium from wastes generated by the processing of irradiated nuclear reactor fuels. This process consists of a cascade of mass transfer stages in which cesium is transferred from an aqueous feed into the CSSX extractant (BOBCalixC6), the extract is scrubbed with 0.05 M nitric acid to remove coextracted elements, and the solvated cesium is stripped (or back-extracted) into 0.001 M HNO{sub 3}. Removal of cesium from stored waste supernatants is desirable as a means of segregating high-activity cesium-137 ({sup 137}Cs) from the solution, thereby reducing the volume of material that must be processed and disposed of as high-level waste. The CSSX process is one of three cesium removal technologies currently being considered for deployment for treatment of wastes that are stored at the U. S. Department of Energy's (USDOE's) Savannah River Site (SRS). The irradiation tests described in this report were designed to simulate the effect of 2 years of continuous solvent irradiation under conditions present in the stripping and extraction sections of the CSSX cascade. Stated simply, the irradiation tests consisted of continuously mixing an aqueous process solution (either simulated SRS waste supernatant or dilute nitric acid) with the CSSX solvent. The aqueous solutions used in testing were spiked with {sup 137}Cs at known activity levels. Test durations were determined based on the activity levels in the experiment and the estimated solvent exposures to radionuclides in a full-scale CSSX facility.

  10. Determination of fenvalerate in tomato by ultrasound-assisted solvent extraction combined with dispersive liquid-liquid microextraction.

    Science.gov (United States)

    Pirsaheb, Meghdad; Ahmadi-Jouibari, Toraj; Fattahi, Nazir; Shamsipur, Mojtaba

    2014-09-01

    Ultrasound-assisted solvent extraction (UASE) combined with dispersive liquid-liquid microextraction based on the solidification of floating organic drop (DLLME-SFO) has been developed for extraction and determination of fenvalerate from tomato samples. Fenvalerate was determined by high-performance liquid-liquid chromatography-ultraviolet detector. Effects of parameters such as type and volume of extraction solvent in the UASE stage, sonication time, type and volume of extraction solvent and disperser solvent in the DLLME-SFO stage, salt addition and pH effect on extraction were studied and optimized. Under the optimum conditions, the calibration graph was linear in the range of 5-500 µg kg(-1) with a detection limit of 0.6 µg kg(-1). The relative standard deviation for five replicate measurements of 100 µg kg(-1) of fenvalerate was 6.5%. The relative recovery of fenvalerate in different tomato samples at a spiking level of 10, 20 and 50 µg kg(-1) is in the range of 93.5-108%. The obtained results show that UASE-DLLME-SFO is a sensitive, fast and simple method for the determination of fenvalerate in tomato samples.

  11. Equilibrium Copper Strip Points as a Function of Temperature and Other Operating Parameters: Implications for Commercial Copper Solvent Extraction Plants

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The development of pressure and bioleaching processes for high grade copper ores and concentrates will result in copper solvent extraction plants treating solutions with high copper and acid concentrations at temperatures up to 45C and these copper solvent extraction plants will run with reagent concentrations up to 40 vol.%. There is also a trend to use copper stripping solutions with less acid than typically used in recent years. Cognis has developed a model that accurately predicts the copper strip point for virtually any copper solvent extraction reagent or combination of reagents under a wide variety of conditions. The equilibrium strip points for several well known commercial copper solvent extraction reagents are given as a function of reagent concentration, the copper and acid concentration of the strip aqueous, and the temperature. It is shown that the equilibrium strip point is not a straight line function of reagent concentration and that the equilibrium strip point increases with an increase in temperature. Copper extraction also increases as the temperature increases.

  12. Optimization of pectinase-assisted and tri-solvent-mediated extraction and recovery of lycopene from waste tomato peels.

    Science.gov (United States)

    Munde, Pravin J; Muley, Abhijeet B; Ladole, Mayur R; Pawar, Amesh V; Talib, Mohammed I; Parate, Vishal R

    2017-07-01

    In the present work, optimization of pectinase-assisted and tri-solvent-mediated extraction of lycopene from waste tomato peels was carried out. The optimized parameters for enzymatic pre-treatment were 2% pectinase concentration, pH 5.5, 4-h incubation, 45 °C and 150 rpm. Maximum recovery of lycopene from tomato peels using optimized tri-solvent extraction was achieved at 45 °C, 120-min incubation and 200 rpm. The extracted lycopene was confirmed through functional and characteristic peaks in UV-Vis and FTIR spectra and with retention time in HPLC. The radical scavenging activity was 72.30 ± 2.70 and 43.40 ± 2.01 µg ascorbic acid equivalents (AAE)/ml for 1,1-diphenyl-2-picrylhydrzyl (DPPH) and 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) radicals, respectively. The optimized method resulted in 7.38, 4.65 and 1.59 times enhancement in lycopene extraction and recovery in correlation with single solvent, enzyme-treated and tri-solvent extraction methods, respectively.

  13. Fractionation of commercial hexane and use of its fractions as extracting solvent of cottonseed oil

    Directory of Open Access Journals (Sweden)

    Megahed, Ola A.

    2001-04-01

    Full Text Available The problem of producing off-graded cottonseed oil using locally produced commercial hexane as extracting solvent has explored this research. It was aimed in this work to investigate whether this problem can be solved by controlling the boiling range of the extracting solvent. Four different hexane fractions of different boiling ranges were prepared from commercial hexane. The boiling range of commercial hexane was 62-68ºC while the boiling ranges of the four fractions were 62- 64, 64-65, 65-66 and 66-68ºC. Commercial hexane and the prepared four hexane fractions were then used to extract cottonseed oil from a fixed seed sample. The five crude oil samples were then refined and bleached and their colours were measured. The results have shown that the heaviest hexane fraction ( b.r 66-68ºC produced the lightest coloured oils. The colour index of the bleached oil using this heavy cut was 190 compared to 350 using the original commercial hexane. However, the production of a commercial hexane cut having a narrow boiling range will be costly. Therefore, this research has been extended to investigate the suitability of a heavy petroleum cut which has a boiling range as wide as that of commercial hexane to extract cottonseed oil. The boiling range of this cut was 66-72ºC. The obtained results proved that the extraction of cottonseed oil using that heavy petroleum fraction produces much lighter oil than the use of conventional hexane solvent.En esta investigación se ha examinado el problema de producir aceite de semilla de algodón sin-clasificar usando hexano comercial producido localmente como disolvente. El objetivo de este trabajo fue investigar si este problema puede ser solucionado controlando el rango de ebullición del disolvente extractante. Cuatro fracciones diferentes de hexano de diversos rangos de ebullición fueron preparadas del hexano comercial. El rango al que ebullía el hexano comercial era 62-68ºC mientras que los

  14. Solvent extraction of rubidium from gold waste using conventional SX and new CFE methods

    Institute of Scientific and Technical Information of China (English)

    Mohammad Reza Tavakoli Mohammadi; Seyed Mohammad Javad Koleini; Sepideh Javanshir; Hossein Abolghasemi; Mahmoud Abdollahy

    2015-01-01

    Solvent extraction (SX) of rubidium (Rb) from leaching filtrate of gold waste (GW) in Mouteh Processing Plant by 18-crown-6 (18C6) was studied.High potential of new column flotoextraction (CFE) method in extraction of Rb from dilute solutions was also demonstrated.First,the factors affecting SX of Rb from a synthetic rubidium sulfate solution (containing 100 mg·L-1 Rb) were identified.0.05 mol·L-1 18C6 in kerosene,0.02 mol·L-1 picric acid in aqueous phase,aqueous to organic (A/O) ratio of 1,pH 7 and mixing time of 15 min are the optimum values for affective factors.The three-stage precipitation with sodium carbonate,pH adjustment with sulfuric acid and two-stage evaporation and crystallization were conducted to purify the leaching from impurities such as Fe,Al,Mn,Ca and especially competing cations of K and Na.Almost complete extraction of Rb and K from final filtrate containing 0.08 mol·L-1 picric acid was performed using 0.2 mol·L-1 18C6 in kerosene.The Rb and K strippings of 99.12 % and 9.93 %,respectively,are obtained with 2 mol·L-1 nitric acid with A/O ratio of 2.Finally,the performance comparison of the CFE and SX methods in similar conditions shows increased extraction of K and Rb by 16 % and 5 %,respectively,using CFE method.

  15. Effect of Extraction Solvents and Drying Methods on the Physicochemical and Antioxidant Properties of Helicteres hirsuta Lour. Leaves

    Directory of Open Access Journals (Sweden)

    Hong Ngoc Thuy Pham

    2015-12-01

    Full Text Available Helicteres hirsuta Lour. (H. hirsuta L. is widely distributed in southeast Asian countries and has been used traditionally as a medicinal plant. However, optimal conditions for preparation of dried materials for further processing and suitable solvents for the extraction of bioactive compounds have not been investigated. The objective of this study was to evaluate the effects of different extraction solvents and different drying conditions on the physicochemical properties and antioxidant capacity of the H. hirsuta L. leaves. The results showed that both extraction solvents and drying conditions had a significant impact on physicochemical and antioxidant properties of H. hirsuta L. leaves. Among the five solvents investigated, water could extract the highest level of solid content and phenolic compounds, whereas methanol was more effective for obtaining flavonoids and saponins than other solvents. The leaves dried under either hot-air drying at 80 °C (HAD80, or vacuum drying at 50 °C (VD50 yielded the highest amount of total phenolic compounds (7.77 and 8.33 mg GAE/g, respectively and total flavonoid content (5.79 and 4.62 mg CE/g, respectively, and possessed the strongest antioxidant power, while leaves dried using infrared drying at 30 °C had the lowest levels of bioactive compounds. Phenolic compounds including flavonoids had a strong correlation with antioxidant capacity. Therefore, HAD80 and VD50 are recommended for the preparation of dried H. hirsuta L. leaves. Water and methanol are suggested solvents to be used for extraction of phenolic compounds and saponins from H. hirsuta L. leaves for the potential application in the nutraceutical and pharmaceutical industries.

  16. Study on Gold(Ⅰ) Solvent Extraction from Alkaline Cyanide Solution by TBP with Addition of Surfactant

    Institute of Scientific and Technical Information of China (English)

    1999-01-01

    The new solvent extraction system for gold(Ⅰ) from alkaline cyanide solution by TBP with addition of surfactant in aqueous phase was studied. The effect of various factors, such as equilibrium pH, constitution of organic phase, molar ratio of CPB∶Au(CN)2-, extraction time, aqueous/organic phase ratio, different initial gold concentration, equilibrium temperature, different diluent, different types of extractants and surfactants etc., was inspected. The results show that gold(Ⅰ) can be extracted quantitatively by controlling the quantity of surfactant (CPB); both the equilibrium pH and diluent hardly influence percent extraction. Gold(Ⅰ) percent extraction reaches more than 98% under the optimal experimental conditions. 30% vol TBP diluted by sulphonating kerosene can load gold(Ⅰ) to rather high levels. Loading capacity is in excess of 38 g/L. The extraction mechanism is discussed and the overall extraction reaction is deduced.

  17. Indium recovery from acidic aqueous solutions by solvent extraction with D2EHPA: a statistical approach to the experimental design

    Directory of Open Access Journals (Sweden)

    Fortes M.C.B.

    2003-01-01

    Full Text Available This experimental work presents the optimization results of obtaining a high indium concentration solution and minimum iron poisoning by solvent extraction with D2EHPA solubilized in isoparaffin and exxsol. The variables studied in the extraction step were D2EHPA concentration, acidity of the aqueous phase and time of contact between phases. Different hydrochloric and sulfuric acid concentrations were studied for the stripping step. The optimum experimental conditions resulted in a solution with 99% indium extraction and less than 4% iron. The construction of a McCabe-Thiele diagram indicated two theoretical countercurrent stages for indium extraction and at least six stages for indium stripping. Finally, the influence of associated metals found in typical sulfate leach liquors from zinc plants was studied. Under the experimental conditions for maximum indium extraction, 96% indium extraction was obtained, iron extraction was about 4% and no Ga, Cu and Zn were co-extracted.

  18. Recovery of Vanadium from H2SO4-HF Acidic Leaching Solution of Black Shale by Solvent Extraction and Precipitation

    Directory of Open Access Journals (Sweden)

    Xingbin Li

    2016-03-01

    Full Text Available The recovery of vanadium from sulfuric and hydrofluoric mixed acid solutions generated by the direct leaching of black shale was investigated using solvent extraction and precipitation methods. The process consisted of reduction, solvent extraction, and stripping, followed by precipitation and calcination to yield vanadium pentoxide. The influence of various operating parameters on the extraction and recovery of vanadium was studied. Vanadium (IV was selectively extracted using a mixture of 10% (v/v di(2-ethylhexylphosphoric acid and 5% (v/v tri-n-butylphosphate in sulfonated kerosene. Using six extraction and five stripping stages, the extraction efficiency for vanadium was 96.7% and the stripping efficiency was 99.7%. V2O5 with a purity of 99.52% was obtained by oxidation of the loaded strip solution and precipitation of ammonium polyvanadate at pH 1.8 to 2.2, followed by calcination of the dried precipitate at 550 °C for 2 h. It was concluded that the combination of solvent extraction and precipitation is an efficient method for the recovery of vanadium from a multi-element leach solution generated from black shale.

  19. Improvement of extraction capability of magnetic molecularly imprinted polymer beads in aqueous media via dual-phase solvent system.

    Science.gov (United States)

    Hu, Yuling; Liu, Ruijin; Zhang, Yi; Li, Gongke

    2009-08-15

    In this study, a novel and simple dual-phase solvent system for the improvement of extraction capability of magnetic molecularly imprinted polymer (MIP) beads in aqueous sample was proposed. The method integrated MIP extraction and micro-liquid-liquid extraction (micro-LLE) into only one step. A magnetic MIP beads using atrazine as template was synthesized, and was applied to aqueous media by adding micro-volume of n-hexane to form a co-extraction system. The magnetic MIP beads preferred to suspend in the organic phase, which shielded them from the disturbance of water molecule. The target analyte