WorldWideScience

Sample records for chlorine iodides

  1. Mechanistic aspects of ingested chlorine dioxide on thyroid function: impact of oxidants on iodide metabolism

    Energy Technology Data Exchange (ETDEWEB)

    Bercz, J.P.; Jones, L.L.; Harrington, R.M.; Bawa, R.; Condie, L.

    1986-11-01

    Toxicological studies dealing with recent findings of health effects of drinking water disinfectants are reviewed. Experiments with monkeys and rodents indicate that the biological activity of ingested disinfectants is expressed via their chemical interaction with the mucosal epithelia, secretory products, and nutritional contents of the alimentary tract. Evidence exists that a principal partner of this redox interaction is the iodide of nutritional origin that is ubiquitous in the gastrointestinal tract. Thus the observation that subchronic exposure to chlorine dioxide (ClO/sub 2/) in drinking water decreases serum thyroxine levels in mammalian species can be best explained with changes produced in the chemical form of the bioavailable iodide. Ongoing and previously reported mechanistic studies indicate that oxidizing agents such as chlorine-based disinfectants oxidize the basal iodide content of the gastrointestinal tract. The resulting reactive iodine species readily attaches to organic matter by covalent bonding. Evidence suggests that the extent to which such iodinated organics are formed is proportional to the magnitude of the electromotive force and stoichiometry of the redox couple between iodide and the disinfectant. Because the extent of thyroid uptake of the bioavailable iodide does not decrease during ClO/sub 2/ ingestion, it seems that ClO/sub 2/ does not cause iodide deficiency of sufficient magnitude to account for the decease in hormonogenesis. Absorption of one or more of iodinated molecules, e.g., nutrient, hormones, or cellular constituents of the alimentary tract having thyromimetic or thyroid inhibitory properties, is a better hypothesis for the effects seen.

  2. Toxic impact of bromide and iodide on drinking water disinfected with chlorine or chloramines.

    Science.gov (United States)

    Yang, Yang; Komaki, Yukako; Kimura, Susana Y; Hu, Hong-Ying; Wagner, Elizabeth D; Mariñas, Benito J; Plewa, Michael J

    2014-10-21

    Disinfectants inactivate pathogens in source water; however, they also react with organic matter and bromide/iodide to form disinfection byproducts (DBPs). Although only a few DBP classes have been systematically analyzed for toxicity, iodinated and brominated DBPs tend to be the most toxic. The objectives of this research were (1) to determine if monochloramine (NH2Cl) disinfection generated drinking water with less toxicity than water disinfected with free chlorine (HOCl) and (2) to determine the impact of added bromide and iodide in conjunction with HOCl or NH2Cl disinfection on mammalian cell cytotoxicity and genomic DNA damage induction. Water disinfected with chlorine was less cytotoxic but more genotoxic than water disinfected with chloramine. For both disinfectants, the addition of Br(-) and I(-) increased cytotoxicity and genotoxicity with a greater response observed with NH2Cl disinfection. Both cytotoxicity and genotoxicity were highly correlated with TOBr and TOI. However, toxicity was weakly and inversely correlated with TOCl. Thus, the forcing agents for cytotoxicity and genotoxicity were the generation of brominated and iodinated DBPs rather than the formation of chlorinated DBPs. Disinfection practices need careful consideration especially when using source waters containing elevated bromide and iodide.

  3. A coupled chemical burster: The chlorine dioxide-iodide reaction in two flow reactors

    Science.gov (United States)

    Dolnik, Milos; Epstein, Irving R.

    1993-01-01

    The dynamical behavior of the chlorine dioxide-iodide reaction has been studied in a system consisting of two continuous flow stirred tank reactors (CSTRs). The reactors are coupled by computer monitoring of the electrochemical potential in each reactor, which is then used to control the input into the other reactor. Two forms of coupling are employed: reciprocally triggered, exponentially decreasing stimulation, and alternating mass exchange. The reaction, which exhibits oscillatory and excitable behavior in a single CSTR, displays neuronlike bursting behavior with both forms of coupling. Reciprocal stimulation yields bursting in both reactors, while with alternating mass exchange, bursting is observed in one reactor and complex oscillation in the other. A simple model of the reaction gives good agreement between the experimental observations and numerical simulations.

  4. Chlorine Dioxide-Iodide-Methyl Acetoacetate Oscillation Reaction Investigated by UV-Vis and Online FTIR Spectrophotometric Method

    Science.gov (United States)

    Shi, Laishun; Wang, Xiaomei; Li, Na; Liu, Jie; Yan, Chunying

    2012-01-01

    In order to study the chemical oscillatory behavior and mechanism of a new chlorine dioxide-iodide ion-methyl acetoacetate reaction system, a series of experiments were done by using UV-Vis and online FTIR spectrophotometric method. The initial concentrations of methyl acetoacetate, chlorine dioxide, potassium iodide, and sulfuric acid and the pH value have great influence on the oscillation observed at wavelength of 289 nm. There is a preoscillatory or induction period, and the amplitude and the number of oscillations are associated with the initial concentration of reactants. The equations for the triiodide ion reaction rate changing with reaction time and the initial concentrations in the oscillation stage were obtained. Oscillation reaction can be accelerated by increasing temperature. The apparent activation energies in terms of the induction period and the oscillation period were 26.02 KJ/mol and 17.65 KJ/mol, respectively. The intermediates were detected by the online FTIR analysis. Based upon the experimental data in this work and in the literature, a plausible reaction mechanism was proposed for the oscillation reaction. PMID:22454614

  5. Chlorine Dioxide-Iodide-Methyl Acetoacetate Oscillation Reaction Investigated by UV-Vis and Online FTIR Spectrophotometric Method

    Directory of Open Access Journals (Sweden)

    Laishun Shi

    2012-01-01

    Full Text Available In order to study the chemical oscillatory behavior and mechanism of a new chlorine dioxide-iodide ion-methyl acetoacetate reaction system, a series of experiments were done by using UV-Vis and online FTIR spectrophotometric method. The initial concentrations of methyl acetoacetate, chlorine dioxide, potassium iodide, and sulfuric acid and the pH value have great influence on the oscillation observed at wavelength of 289 nm. There is a preoscillatory or induction period, and the amplitude and the number of oscillations are associated with the initial concentration of reactants. The equations for the triiodide ion reaction rate changing with reaction time and the initial concentrations in the oscillation stage were obtained. Oscillation reaction can be accelerated by increasing temperature. The apparent activation energies in terms of the induction period and the oscillation period were 26.02 KJ/mol and 17.65 KJ/mol, respectively. The intermediates were detected by the online FTIR analysis. Based upon the experimental data in this work and in the literature, a plausible reaction mechanism was proposed for the oscillation reaction.

  6. Chlorine doping reduces electron-hole recombination in lead iodide perovskites: time-domain ab initio analysis.

    Science.gov (United States)

    Liu, Jin; Prezhdo, Oleg V

    2015-11-19

    Rapid development in lead halide perovskites has led to solution-processable thin film solar cells with power conversion efficiencies close to 20%. Nonradiative electron-hole recombination within perovskites has been identified as the main pathway of energy losses, competing with charge transport and limiting the efficiency. Using nonadiabatic (NA) molecular dynamics, combined with time-domain density functional theory, we show that nonradiative recombination happens faster than radiative recombination and long-range charge transfer to an acceptor material. Doping of lead iodide perovskites with chlorine atoms reduces charge recombination. On the one hand, chlorines decrease the NA coupling because they contribute little to the wave functions of the valence and conduction band edges. On the other hand, chlorines shorten coherence time because they are lighter than iodines and introduce high-frequency modes. Both factors favor longer excited-state lifetimes. The simulation shows good agreement with the available experimental data and contributes to the comprehensive understanding of electronic and vibrational dynamics in perovskites. The generated insights into design of higher-efficiency solar cells range from fundamental scientific principles, such as the role of electron-vibrational coupling and quantum coherence, to practical guidelines, such as specific suggestions for chemical doping.

  7. Formation of iodinated disinfection by-products during oxidation of iodide-containing waters with chlorine dioxide.

    Science.gov (United States)

    Ye, Tao; Xu, Bin; Lin, Yi-Li; Hu, Chen-Yan; Lin, Lin; Zhang, Tian-Yang; Gao, Nai-Yun

    2013-06-01

    This study was to explore the formation of iodinated disinfection by-products (I-DBPs), including iodoform (CHI3), iodoacetic acid (IAA) and triiodoacetic acid (TIAA), when iodide-containing artificial synthesized waters and raw waters are in contact with chlorine dioxide (ClO2). Among the investigated I-DBPs, CHI3 was the major species during ClO2 oxidation in artificial synthesized waters. Impact factors were evaluated, including the concentrations of ClO2, iodide (I(-)), dissolved organic carbon (DOC) and pH. Formation of CHI3, IAA and TIAA followed an increasing and then decreasing pattern with increased ClO2 or DOC concentration. I-DBPs yield was significantly affected by solution pH. High concentrations of I-DBPs were generated under circumneutral conditions with the maximum formation at pH 8. The increase of I(-) concentration can increase I-DBPs yields, but the increment was suppressed when I(-) concentration was higher than 50 μM. When 100 μg/L I(-)and ClO2 (7.5-44.4 μM) were spiked to the raw water samples from Yangshupu and Minhang drinking water treatment plant, certain amounts of CHI3 and IAA were found under pH 7 and the concentrations were strongly correlated with ClO2 dosage and water qualities, however, no TIAA was detected. Finally, we investigated I-DBPs formation of 18 model compounds, including 4 carboxylic acids, 5 phenols and 8 amino acids, treating with ClO2 when I(-) was present. Results showed that most of these model compounds could form a considerable amount of I-DBPs, especially for propanoic acid, butanoic acid, resorcinol, hydroquinone, alanine, glutamic acid, phenylalanine and serine.

  8. Experimental Study of Closed System in the Chlorine Dioxide-Iodide-Sulfuric Acid Reaction by UV-Vis Spectrophotometric Method

    Science.gov (United States)

    Li, Na; Shi, Laishun; Wang, Xiaomei; Guo, Fang; Yan, Chunying

    2011-01-01

    The mole ratio r(r = [I−]0/[ClO2]0) has great influence on ClO2-I−-H2SO4 closed reaction system. By changing the initiate concentration of potassium iodide, the curve of absorbance along with the reaction time was obtained at 350 nm and 297 nm for triiodide ion, and 460 nm for iodine. The changing point of the absorbance curve's shape locates at r = 6.00. For the reaction of ClO2-I− in the absence of H2SO4, the curve of absorbance along with the reaction time can be obtained at 350 nm for triiodide ion, 460 nm for iodine. The mole ratio r is equal to 1.00 is the changing point of the curve's shape no matter at which wavelength to determine the reaction. For the reaction of ClO2-I−-H+ in different pH buffer solution, the curve of absorbance along with the reaction time was recorded at 460 nm for iodine. When r is greater than 1.00, the transition point of the curve's shape locates at pH 2.0, which is also the point of producing chlorite or chloride for chlorine dioxide at different pH. When r is less than 1.00, the transition point locates at pH 7.0. PMID:21808646

  9. Experimental Study of Closed System in the Chlorine Dioxide-Iodide-Sulfuric Acid Reaction by UV-Vis Spectrophotometric Method

    Directory of Open Access Journals (Sweden)

    Na Li

    2011-01-01

    Full Text Available The mole ratio r(r=[I−]0/[ClO2]0 has great influence on ClO2-I−-H2SO4 closed reaction system. By changing the initiate concentration of potassium iodide, the curve of absorbance along with the reaction time was obtained at 350 nm and 297 nm for triiodide ion, and 460 nm for iodine. The changing point of the absorbance curve's shape locates at r=6.00. For the reaction of ClO2-I− in the absence of H2SO4, the curve of absorbance along with the reaction time can be obtained at 350 nm for triiodide ion, 460 nm for iodine. The mole ratio r is equal to 1.00 is the changing point of the curve's shape no matter at which wavelength to determine the reaction. For the reaction of ClO2-I−-H+ in different pH buffer solution, the curve of absorbance along with the reaction time was recorded at 460 nm for iodine. When r is greater than 1.00, the transition point of the curve's shape locates at pH 2.0, which is also the point of producing chlorite or chloride for chlorine dioxide at different pH. When r is less than 1.00, the transition point locates at pH 7.0.

  10. Chlorination of iodide-containing waters in the presence of CuO: formation of periodate.

    Science.gov (United States)

    Liu, Chao; Salhi, Elisabeth; Croué, Jean-Philippe; von Gunten, Urs

    2014-11-18

    It has been shown previously that the disproportionation of halogen-containing oxidants (e.g., HOCl, HOBr, and ClO2) is enhanced by a CuO-catalyzed process. In this study, the transformation of iodine during chlorination in the presence of CuO was investigated. There is no significant enhancement of the disproportionation of hypoiodous acid (HOI) in the presence of CuO. The formation rate of iodate (IO3(-)) in the CuO-HOCl-I(-) system significantly increased when compared to homogeneous solutions, which was ascribed to the activation of HOCl by CuO enhancing its reactivity toward HOI. In this reaction system, iodate formation rates increase with increasing CuO (0-0.5 g L(-1)) and bromide (0-2 μM) doses and with decreasing pH (9.6-6.6). Iodate does not adsorb to the CuO surfaces used in this study. Nevertheless, iodate concentrations decreased after a maximum was reached in the CuO-HOCl-I(-)(-Br(-)) systems. Similarly, the iodate concentrations decrease as a function of time in the CuO-HOCl-IO3(-) or CuO-HOBr-IO3(-) system, and the rates increase with decreasing pH (9.6-6.6) due to the enhanced reactivity of HOCl or HOBr in the presence of CuO. It could be demonstrated that iodate is oxidized to periodate by a CuO-activated hypohalous acid, which is adsorbed on the CuO surface. No periodate could be measured in filtered solutions because it was mainly adsorbed to CuO. The adsorbed periodate was identified by scanning electron microscopy plus energy dispersive spectroscopy and X-ray photoelectron spectroscopy.

  11. Chlorination of iodide-containing waters in the presence of CuO: Formation of periodate

    KAUST Repository

    Liu, Chao

    2014-11-18

    It has been shown previously that the disproportionation of halogen-containing oxidants (e.g., HOCl, HOBr, and ClO2) is enhanced by a CuO-catalyzed process. In this study, the transformation of iodine during chlorination in the presence of CuO was investigated. There is no significant enhancement of the disproportionation of hypoiodous acid (HOI) in the presence of CuO. The formation rate of iodate (IO3 -) in the CuO-HOCl-I- system significantly increased when compared to homogeneous solutions, which was ascribed to the activation of HOCl by CuO enhancing its reactivity toward HOI. In this reaction system, iodate formation rates increase with increasing CuO (0-0.5 g L-1) and bromide (0-2 μM) doses and with decreasing pH (9.6-6.6). Iodate does not adsorb to the CuO surfaces used in this study. Nevertheless, iodate concentrations decreased after a maximum was reached in the CuO-HOCl-I-(-Br-) systems. Similarly, the iodate concentrations decrease as a function of time in the CuO-HOCl-IO3 - or CuO-HOBr-IO3 - system, and the rates increase with decreasing pH (9.6-6.6) due to the enhanced reactivity of HOCl or HOBr in the presence of CuO. It could be demonstrated that iodate is oxidized to periodate by a CuO-activated hypohalous acid, which is adsorbed on the CuO surface. No periodate could be measured in filtered solutions because it was mainly adsorbed to CuO. The adsorbed periodate was identified by scanning electron microscopy plus energy dispersive spectroscopy and X-ray photoelectron spectroscopy.

  12. Chlorine

    Science.gov (United States)

    ... but it is also used to make pesticides (insect killers), rubber, and solvents. Chlorine is used in ... the following signs and symptoms may develop: Blurred vision Burning pain, redness, and blisters on the skin ...

  13. Chlorine

    Energy Technology Data Exchange (ETDEWEB)

    Talmage, Sylvia Smith [ORNL

    2009-01-01

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

  14. Potassium Iodide

    Science.gov (United States)

    Potassium iodide is used to protect the thyroid gland from taking in radioactive iodine that may be released ... damage the thyroid gland. You should only take potassium iodide if there is a nuclear radiation emergency and ...

  15. Potassium Iodide (KI)

    Science.gov (United States)

    ... Health Matters Information on Specific Types of Emergencies Potassium Iodide (KI) Language: English Español (Spanish) Recommend on Facebook ... can I get KI (potassium iodide)? What is Potassium Iodide (KI)? KI (potassium iodide) is a salt of ...

  16. A comparison of iodinated trihalomethane formation from chlorine, chlorine dioxide and potassium permanganate oxidation processes.

    Science.gov (United States)

    Zhang, Tian-Yang; Xu, Bin; Hu, Chen-Yan; Lin, Yi-Li; Lin, Lin; Ye, Tao; Tian, Fu-Xiang

    2015-01-01

    This study compared the formation of iodinated trihalomethanes (I-THMs) from iodide-containing raw waters oxidized by chlorine, chlorine dioxide (ClO₂) and potassium permanganate (KMnO₄) at different oxidant concentrations, reaction times, pHs, initial iodide concentrations and bromide to iodide mass ratios. Among the six investigated I-THMs, iodoform was the major species formed during the oxidation using chlorine, ClO₂ and KMnO₄. When oxidant concentration increased from 0.1 to 3.0 mg/L, the formation of I-THMs increased and then decreased for chlorine and ClO₂, but kept increasing for KMnO₄. As the reaction time went by, I-THM concentration increased to a plateau within 10 h (ClO₂ within only 1 h, especially) for all the three oxidants. I-THM formation gradually increased from pH 3.0 to 9.0 and remained stable at pH values higher than 7.5 for chlorine; however, for ClO₂ and KMnO₄ the highest I-THM formation showed at pH 7.0 and 7.5, respectively. As initial iodide concentration increased from 20 to 800 μg/L, the total amount and species of I-THMs increased for the three oxidants. Iodide contributed to I-THM formation much more significantly than bromide.

  17. Methyl Iodide Fumigation of Bacillus anthracis Spores.

    Science.gov (United States)

    Sutton, Mark; Kane, Staci R; Wollard, Jessica R

    2015-09-01

    Fumigation techniques such as chlorine dioxide, vaporous hydrogen peroxide, and paraformaldehyde previously used to decontaminate items, rooms, and buildings following contamination with Bacillus anthracis spores are often incompatible with materials (e.g., porous surfaces, organics, and metals), causing damage or residue. Alternative fumigation with methyl bromide is subject to U.S. and international restrictions due to its ozone-depleting properties. Methyl iodide, however, does not pose a risk to the ozone layer and has previously been demonstrated as a fumigant for fungi, insects, and nematodes. Until now, methyl iodide has not been evaluated against Bacillus anthracis. Sterne strain Bacillus anthracis spores were subjected to methyl iodide fumigation at room temperature and at 550C. Efficacy was measured on a log-scale with a 6-log reduction in CFUs being considered successful compared to the U.S. Environmental Protection Agency biocide standard. Such efficacies were obtained after just one hour at 55 °C and after 12 hours at room temperature. No detrimental effects were observed on glassware, PTFE O-rings, or stainless steel. This is the first reported efficacy of methyl iodide in the reduction of Bacillus anthracis spore contamination at ambient and elevated temperatures.

  18. dl-Alaninium iodide

    Directory of Open Access Journals (Sweden)

    Kevin Lamberts

    2012-06-01

    Full Text Available The crystal structure of dl-alanine hydroiodide (1-carboxyethanaminium iodide, C3H8NO2+·I−, is that of an organic salt consisting of N-protonated cations and iodide anions. The compound features homochiral helices of N—H...O hydrogen-bonded cations in the [010] direction; neighbouring chains are related by crystallographic inversion centers and hence show opposite chirality. The iodide counter-anions act as hydrogen-bond acceptors towards H atoms of the ammonium and carboxy groups, and cross-link the chains along [100]. Thus, an overall two-dimensional network is formed in the ab plane. No short contacts occur between iodide anions.

  19. Enhanced Olefin Cross Metathesis Reactions: The Copper Iodide Effect

    Science.gov (United States)

    Voigtritter, Karl; Ghorai, Subir

    2011-01-01

    Copper iodide has been shown to be an effective co-catalyst for the olefin cross metathesis reaction. In particular, it has both a catalyst stabilizing effect due to iodide ion, as well as copper(I)-based phosphine-scavenging properties that apply to use of the Grubbs-2 catalyst. A variety of Michael acceptors and olefinic partners can be cross-coupled under mild conditions in refluxing diethyl ether that avoid chlorinated solvents. This effect has also been applied to chemistry in water at room temperature using the new surfactant TPGS-750-M. PMID:21528868

  20. 21 CFR 184.1265 - Cuprous iodide.

    Science.gov (United States)

    2010-04-01

    ... with potassium iodide under slightly acidic conditions. (b) The ingredient must be of a purity suitable... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Cuprous iodide. 184.1265 Section 184.1265 Food and... Substances Affirmed as GRAS § 184.1265 Cuprous iodide. (a) Cuprous iodide (copper (I) iodide, CuI, CAS...

  1. Synthesis of mercuric iodide and bismuth tri-iodide nanoparticles for heavy metal iodide films nucleation

    Energy Technology Data Exchange (ETDEWEB)

    Fornaro, L.; Pereira, H.Bentos [Compound Semiconductors Group, CURE, Universidad de la Republica, Rocha (Uruguay); Aguiar, I.; Perez Barthaburu, M. [Compound Semiconductors Group, Facultad de Quimica, Univ. de la Republica, Montevideo (Uruguay)

    2011-12-15

    We synthesized mercuric iodide and bismuth tri-iodide nanoparticles by suspension in octadecene, from Hg(NO{sub 3}){sub 2}.H{sub 2}O and I{sub 2}, and from Bi(NO{sub 3}){sub 3}.5H{sub 2}O and I{sub 2}, respectively. The best synthesis conditions were 2 h at 70-80 C, followed by 10 min at 110 C for mercuric iodide nanoparticles, and 4 h at 80-110 C, followed by 10 min at 180-210 C for bismuth tri-iodide ones. Nanoparticles were then washed and centrifuged with ether repeatedly. Compounds identity was confirmed by X-ray diffraction (XRD) and energy dispersive spectrometry (EDS). We found shifts of the X-ray diffraction maxima for nanoparticles of both compounds. We characterized the nanoparticles by transmission (TEM) and scanning (SEM) electron microscopy. We obtained disk-like and squared mercuric iodide nanostructures, 80-140 nm and 100-125 nm in size respectively. We also obtained rounded and rod-like bismuth tri-iodide nanoparticles, 30-500 nm in size. Acetonitrile and isopropanol suspensions of mercuric iodide nanoparticles, and acetonitrile suspension of bismuth tri-iodide nanoparticles exhibited peak maxima shifts in their UV-Vis spectra. We synthesized for the first time mercuric iodide and bismuth tri-iodide nanoparticles by the suspension method, although we have not yet obtained uniform shape and size distributions. They offer interesting perspectives for crystalline film nucleation and for improving current applications of these materials, as well as for opening new ones. (copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  2. 21 CFR 172.375 - Potassium iodide.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Potassium iodide. 172.375 Section 172.375 Food and... Dietary and Nutritional Additives § 172.375 Potassium iodide. The food additive potassium iodide may be safely used in accordance with the following prescribed conditions: (a) Potassium iodide may be...

  3. Iodide transport and breast cancer.

    Science.gov (United States)

    Poole, Vikki L; McCabe, Christopher J

    2015-10-01

    Breast cancer is the second most common cancer worldwide and the leading cause of cancer death in women, with incidence rates that continue to rise. The heterogeneity of the disease makes breast cancer exceptionally difficult to treat, particularly for those patients with triple-negative disease. To address the therapeutic complexity of these tumours, new strategies for diagnosis and treatment are urgently required. The ability of lactating and malignant breast cells to uptake and transport iodide has led to the hypothesis that radioiodide therapy could be a potentially viable treatment for many breast cancer patients. Understanding how iodide is transported, and the factors regulating the expression and function of the proteins responsible for iodide transport, is critical for translating this hypothesis into reality. This review covers the three known iodide transporters - the sodium iodide symporter, pendrin and the sodium-coupled monocarboxylate transporter - and their role in iodide transport in breast cells, along with efforts to manipulate them to increase the potential for radioiodide therapy as a treatment for breast cancer.

  4. Detection, identification and formation of new iodinated disinfection byproducts in chlorinated saline wastewater effluents.

    Science.gov (United States)

    Gong, Tingting; Zhang, Xiangru

    2015-01-01

    The use of seawater for toilet flushing introduces high levels of inorganic ions, including iodide ions, into a city's wastewater treatment systems, resulting in saline wastewater effluents. Chlorination is widely used in disinfecting wastewater effluents owing to its low cost and high efficiency. During chlorination of saline wastewater effluents, iodide may be oxidized to hypoiodous acid, which may further react with effluent organic matter to form iodinated disinfection byproducts (DBPs). Iodinated DBPs show significantly higher toxicity than their brominated and chlorinated analogues and thus have been drawing increasing concerns. In this study, polar iodinated DBPs were detected in chlorinated saline wastewater effluents using a novel precursor ion scan method. The major polar iodinated DBPs were identified and quantified, and their organic precursors and formation pathways were investigated. The formation of iodinated DBPs under different chlorine doses and contact times was also studied. The results indicated that a few polar iodinated DBPs were generated in the chlorinated saline primary effluent, but few were generated in the chlorinated saline secondary effluent. Several major polar iodinated DBPs in the chlorinated saline primary effluent were proposed with structures, among which a new group of polar iodinated DBPs, iodo-trihydroxybenzenesulfonic acids, were identified and quantified. The organic precursors of this new group of DBPs were found to be 4-hydroxybenzenesulfonic acid and 1,2,3-trihydroxybenzene, and the formation pathways of these new DBPs were tentatively proposed. Both chlorine dose and contact time affected the formation of iodinated DBPs in the chlorinated saline wastewater effluents.

  5. Frequently Asked Questions on Potassium Iodide (KI)

    Science.gov (United States)

    ... Bioterrorism and Drug Preparedness Frequently Asked Questions on Potassium Iodide (KI) Share Tweet Linkedin Pin it More sharing ... Drug Administration (FDA) issued a final Guidance on Potassium Iodide as a Thyroid Blocking Agent in Radiation Emergencies) ( ...

  6. 21 CFR 582.5634 - Potassium iodide.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Potassium iodide. 582.5634 Section 582.5634 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Supplements 1 § 582.5634 Potassium iodide. (a) Product. Potassium iodide. (b) Tolerance. 0.01 percent....

  7. 21 CFR 184.1634 - Potassium iodide.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Potassium iodide. 184.1634 Section 184.1634 Food... Specific Substances Affirmed as GRAS § 184.1634 Potassium iodide. (a) Potassium iodide (KI, CAS Reg. No. 7681-11-0) is the potassium salt of hydriodic acid. It occurs naturally in sea water and in...

  8. Effect of chlorine, blanching, freezing, and microwave heating on Cryptosporidium parvum viability inoculated on green peppers.

    Science.gov (United States)

    Duhain, G L M C; Minnaar, A; Buys, E M

    2012-05-01

    Cryptosporidium parvum oocysts have been found on the surface of vegetables in both developed and developing countries. C. parvum can contaminate vegetables via various routes, including irrigation water. This study investigated the effect of individual treatments of chlorine, blanching, blast freezing, and microwave heating, as well as combined treatments of chlorine and freezing, and chlorine and microwave heating on the viability of C. parvum oocysts inoculated on green peppers. The viability of the oocysts after the treatments was assessed using propidium iodide and a flow cytometer. Based on the propidium iodide staining, the chlorine treatments did not affect the viability of the oocysts. Blast freezing significantly inactivated 20% of the oocysts. Microwave heating and blanching significantly inactivated 93% of oocysts. Treatment with chlorine followed by blast freezing did not affect the viability of the oocysts significantly. Treatment with chlorine and microwave heating was significantly more effective than microwave heating alone and inactivated 98% of the oocysts. The study indicates that C. parvum oocysts are sensitive to heat and, to some extent, to blast freezing, but are resistant to chlorine. Therefore, the use of chlorine during vegetable processing is not a critical control point for C. parvum oocysts, and the consumption of raw or minimally processed vegetables may constitute a health risk as C. parvum oocysts can still be found viable on ready-to-eat, minimally processed vegetables.

  9. [Rare, severe hypersensitivity reaction to potassium iodide].

    Science.gov (United States)

    Korsholm, Anne Sofie; Ebbehøj, Eva; Richelsen, Bjørn

    2014-07-07

    The literature reports a large variety of adverse reactions to potassium iodide. A severe hypersensitivity reaction to potassium iodide in a 51-year-old woman with Graves' thyrotoxicosis is described. Following administration the patient developed sialadenitis, conjunctivitis, stomatitis and acneiform iododerma that responded dramatically to withdrawal of the potassium iodide and administration with corticosteroids. Awareness of these adverse reactions may prevent prolonged hospitalization and unnecessary tests and treatments.

  10. Uptake of iodide in the marine haptophyte Isochrysis sp. (T.ISO) driven by iodide oxidation.

    Science.gov (United States)

    van Bergeijk, Stef A; Hernández Javier, Laura; Heyland, Andreas; Manchado, Manuel; Pedro Cañavate, José

    2013-08-01

    Uptake of iodide was studied in the marine microalga Isochrysis sp. (isol. Haines, T.ISO) during short-term incubations with radioactive iodide ((125) I(-) ). Typical inhibitors of the sodium/iodide symporter (NIS) did not inhibit iodide uptake, suggesting that iodide is not taken up through this transport protein, as is the case in most vertebrate animals. Oxidation of iodide was found to be an essential step for its uptake by T.ISO and it seemed likely that hypoiodous acid (HOI) was the form of iodine taken up. Uptake of iodide was inhibited by the addition of thiourea and of other reducing agents, like L-ascorbic acid, L-glutathione and L-cysteine and increased after the addition of oxidized forms of the transition metals Fe and Mn. The simultaneous addition of both hydrogen peroxide (H2 O2 ) and a known iodide-oxidizing myeloperoxidase (MPO) significantly increased iodine uptake, but the addition of H2 O2 or MPO separately, had no effect on uptake. This confirms the observation that iodide is oxidized prior to uptake, but it puts into doubt the involvement of H2 O2 excretion and membrane-bound or extracellular haloperoxidase activity of T.ISO. The increase of iodide uptake by T.ISO upon Fe(III) addition suggests the nonenzymatic oxidation of iodide by Fe(III) in a redox reaction and subsequent influx of HOI. This is the first report on the mechanism of iodide uptake in a marine microalga.

  11. Neutron Detection with Mercuric Iodide

    CERN Document Server

    Bell, Z A

    2003-01-01

    Mercuric iodide is a high-density, high-Z semiconducting material useful for gamma ray detection. This makes it convertible to a thermal neutron detector by covering it with a boron rich material and detecting the 478 keV gamma rays resulting from the sup 1 sup 0 B(n, alpha) sup 7 Li* reaction. However, the 374 barn thermal capture cross section of sup n sup a sup t Hg, makes the detector itself an attractive absorber, and this has been exploited previously. Since previous work indicates that there are no low-energy gamma rays emitted in coincidence with the 368 keV capture gamma from the dominant sup 1 sup 9 sup 9 Hg(n, gamma) sup 2 sup 0 sup 0 Hg reaction, only the 368 keV capture gamma is seen with any efficiency a relatively thin (few mm) detector. In this paper we report preliminary measurements of neutrons via capture reactions in a bare mercuric iodide crystal and a crystal covered in sup 1 sup 0 B-loaded epoxy. The covered detector is an improvement over the bare detector because the presence of both ...

  12. Characterization of unknown iodinated disinfection byproducts during chlorination/chloramination using ultrahigh resolution mass spectrometry.

    Science.gov (United States)

    Wang, Xin; Wang, Juan; Zhang, Yahe; Shi, Quan; Zhang, Haifeng; Zhang, Yu; Yang, Min

    2016-06-01

    Iodinated disinfection byproducts (I-DBPs), formed from the reaction of disinfectant(s) with organic matter in the presence of iodide in raw water, have recently been focused because of their more cytotoxic and genotoxic properties than their chlorinated or brominated analogues. To date, only a few I-DBPs in drinking water have been identified. In this study, C18 solid phase extraction coupled with electrospray ionization ultrahigh resolution Fourier transform ion cyclotron resonance mass spectrometry (ESI FT-ICR MS) was used to characterize unknown I-DBPs in chloraminated/chlorinated water spiked with iodide and humic substances. In total, 178 formulas for one-iodine-containing products, 13 formulas for two-iodine-containing products, and 15 formulas for one-chlorine and one-iodine-containing products were detected in the chloraminated water sample, while only 9 formulas for one-iodine-containing products and 6 formulas for one-chlorine and one-iodine-containing products were found in the chlorinated water sample. Most I-DBPs have corresponding chlorine-containing analogues with identical CHO compositions. As indicated by the modified aromaticity index (AImod), in the C18 extracts, more than 68% of the I-DBPs have aromatic structures or polycyclic aromatic structures. This result demonstrates that the use of chloramination as an alternative disinfection method may lead to the formation of abundant species of I-DBPs in the presence of iodide. Thus, the suitability of adopting chloramination as an alternative disinfection method should be reevaluated, particularly when iodide is present in raw water.

  13. Predissociation dynamics of lithium iodide

    CERN Document Server

    Schmidt, H; Stienkemeier, F; Bogomolov, A S; Baklanov, A V; Reich, D M; Skomorowski, W; Koch, C P; Mudrich, M

    2015-01-01

    The predissociation dynamics of lithium iodide (LiI) in the first excited A-state is investigated for molecules in the gas phase and embedded in helium nanodroplets, using femtosecond pump-probe photoionization spectroscopy. In the gas phase, the transient Li+ and LiI+ ion signals feature damped oscillations due to the excitation and decay of a vibrational wave packet. Based on high-level ab initio calculations of the electronic structure of LiI and simulations of the wave packet dynamics, the exponential signal decay is found to result from predissociation predominantly at the lowest avoided X-A potential curve crossing, for which we infer a coupling constant V=650(20) reciprocal cm. The lack of a pump-probe delay dependence for the case of LiI embedded in helium nanodroplets indicates fast droplet-induced relaxation of the vibrational excitation.

  14. Predissociation dynamics of lithium iodide

    Energy Technology Data Exchange (ETDEWEB)

    Schmidt, H.; Vangerow, J. von; Stienkemeier, F.; Mudrich, M., E-mail: mudrich@physik.uni-freiburg.de [Physikalisches Institut, Universität Freiburg, 79104 Freiburg (Germany); Bogomolov, A. S. [Institute of Chemical Kinetics and Combustion, Novosibirsk 630090 (Russian Federation); Baklanov, A. V. [Institute of Chemical Kinetics and Combustion, Novosibirsk 630090 (Russian Federation); Novosibirsk State University, Novosibirsk 630090 (Russian Federation); Reich, D. M.; Skomorowski, W.; Koch, C. P. [Theoretische Physik, Universität Kassel, Heinrich-Plett-Str. 40, 34132 Kassel (Germany)

    2015-01-28

    The predissociation dynamics of lithium iodide (LiI) in the first excited A-state is investigated for molecules in the gas phase and embedded in helium nanodroplets, using femtosecond pump-probe photoionization spectroscopy. In the gas phase, the transient Li{sup +} and LiI{sup +} ion signals feature damped oscillations due to the excitation and decay of a vibrational wave packet. Based on high-level ab initio calculations of the electronic structure of LiI and simulations of the wave packet dynamics, the exponential signal decay is found to result from predissociation predominantly at the lowest avoided X-A potential curve crossing, for which we infer a coupling constant V{sub XA} = 650(20) cm{sup −1}. The lack of a pump-probe delay dependence for the case of LiI embedded in helium nanodroplets indicates fast droplet-induced relaxation of the vibrational excitation.

  15. Water Treatment Technology - Chlorination.

    Science.gov (United States)

    Ross-Harrington, Melinda; Kincaid, G. David

    One of twelve water treatment technology units, this student manual on chlorination provides instructional materials for nine competencies. (The twelve units are designed for a continuing education training course for public water supply operators.) The competencies focus on the following areas: purpose and process of chlorination, chlorine…

  16. Reaction products of chlorine dioxide.

    OpenAIRE

    Stevens, A A

    1982-01-01

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

  17. Factors affecting the formation of iodo-trihalomethanes during oxidation with chlorine dioxide.

    Science.gov (United States)

    Guo, Wanhong; Shan, Yingchun; Yang, Xin

    2014-01-15

    Effects of water characteristics, reaction time, temperature, bromide and iodide ion concentrations, oxidant doses, and pH on formation of iodinated trihalomethanes (I-THM) during oxidation of iodide-containing water with chlorine dioxide (ClO2) were investigated. Among the water samples collected from ten water sources, iodoform (CHI3) was the predominant I-THM and trace amount of chlorodiiodomethane (CHClI2) was occasionally found. CHI3 yields correlated moderately with specific UV absorbance (SUVA) (R(2)=0.79), indicating that hydrophobic aromatic content were important precursors. Longer reaction time led to continued formation of CHI3. I-THM containing bromide was also found in waters containing both bromide and iodide, but CHI3 was dominant. The formation of CHI3 was higher at 25°C than 5°C and 35°C. CHI3 formation showed an increase followed by a decrease trend with increasing ClO2 doses and iodide concentrations and the highest yields occurred at iodide to ClO2 molar ratios of 1-2. pH 8 resulted in the highest CHI3 formation. It should be noted that a high iodide concentration was spiked to waters before adding ClO2 and the results may not reflect the formation yields of iodinated THMs in real conditions, but they provide information about formation trend of I-THM during oxidation of ClO2.

  18. Sequential flow injection determination of chlorine species using a triiodide-selective electrode detector.

    Science.gov (United States)

    Saad, Bahruddin; Wai, Wan Tatt; Ali, Abdussalam Salhin M; Saleh, Muhammad Idiris

    2006-01-01

    A flow injection analysis (FIA) method for the determination of four residual chlorine species, namely combined available chlorine (CAC), free available chlorine (FAC), total available chlorine (TAC) and chlorite (ClO2-) was developed using a flow-through triiodide-selective electrode as a detector. An important strategy of speciation studies utilized the kinetic discrimination of reactions between the CAC and FAC with Fe2+, which was applied to the speciation of FAC, CAC and TAC. The speciation of available chlorine species and chlorite (an oxychlorine species) was achieved by using the same set-up, but using flow streams of different pH. The effects of the pH of the carrier stream, the flow rate and the sample volume were studied. The method exhibited linearity from 2.8 x 10(-6) to 2.8 x 10(-4) M active chlorine (expressed as OCl-) with a detection limit of 1.4 x 10(-6) M. The selectivity of the method was studied by examining the minimum pH for the oxidation of iodide by other oxidants, and also by assessing the potentiometric selectivity coefficients. The proposed method was successfully applied to the determination of chlorine species in tap water, and disinfecting formulations where good agreement occurred between the proposed and standard methods were found.

  19. Chlorine, Chloramine, Chlorine Dioxide, and Ozone Susceptibility of Mycobacterium avium

    OpenAIRE

    Taylor, Robert H; Falkinham, Joseph O.; Norton, Cheryl D.; LeChevallier, Mark W.

    2000-01-01

    Environmental and patient isolates of Mycobacterium avium were resistant to chlorine, monochloramine, chlorine dioxide, and ozone. For chlorine, the product of the disinfectant concentration (in parts per million) and the time (in minutes) to 99.9% inactivation for five M. avium strains ranged from 51 to 204. Chlorine susceptibility of cells was the same in washed cultures containing aggregates and in reduced aggregate fractions lacking aggregates. Cells of the more slowly growing strains wer...

  20. Reaction products of chlorine dioxide.

    Science.gov (United States)

    Stevens, A A

    1982-01-01

    Inspection of the available literature reveals that a detailed investigation of the aqueous organic chemistry of chlorine dioxide and systematic identification of products formed during water disinfection has not been considered. This must be done before an informed assessment can be made of the relative safety of using chlorine dioxide as a disinfectant alternative to chlorine. Although trihalomethanes are generally not formed by the action of chlorine dioxide, the products of chlorine dioxide treatment of organic materials are oxidized species, some of which also contain chlorine. The relative amounts of species types may depend on the amount of chlorine dioxide residual maintained and the concentration and nature of the organic material present in the source water. The trend toward lower concentrations of chlorinated by-products with increasing ClO2 concentration, which was observed with phenols, has not been observed with natural humic materials as measured by the organic halogen parameter. Organic halogen concentrations have been shown to increase with increasing chlorine dioxide dose, but are much lower than those observed when chlorine is applied. Aldehydes have been detected as apparent by-products of chlorine dioxide oxidation reactions in a surface water that is a drinking water source. Some other nonchlorinated products of chlorine dioxide treatment may be quinones and epoxides. The extent of formation of these moieties within the macromolecular humic structure is also still unknown. PMID:7151750

  1. Simplest Formula of Copper Iodide: A Stoichiometry Experiment.

    Science.gov (United States)

    MacDonald, D. J.

    1983-01-01

    Describes an experiment presented to students as a problem in determining the stoichiometry of "copper iodide" to decide whether it is cuprous iodide or cupric iodide. The experiment illustrates stoichiometry principles, providing experiences with laboratory techniques and numerical computation. Detailed outline (written for student use) is…

  2. Electrochemical reaction rates in a dye sentisised solar cell - the iodide/tri-iodide redox system

    DEFF Research Database (Denmark)

    Bay, Lasse; West, Keld; Winter-Jensen, Bjørn

    2006-01-01

    The electrochemical reaction rate of the redox couple iodide / tri-iodide in acetonitrile is characterised by impedance spectroscopy. Different electrode materials relevant for the function of dye-sensitised solar cells (DSSC) are investigated. Preferably, the reaction with the iodide / tri......-iodide couple should be fast at the counter electrode, i.e. this electrode must have a high catalytic activity towards the redox couple, and the same reaction must be slow on the photo electrode. The catalytic activity is investigated for platinum, poly(3,4-ethylenedioxythiophene) (PEDOT), polypyrrole (PPy......), and polyaniline (PANI) - all deposited onto fluorine doped tin oxide (FTO) glass. Both Pt and PEDOT are found to have sufficiently high catalytic activities for practical use as counter electrode in DSSC. The reaction resistance on FTO and anatase confirmed the beneficial effect of a compact anatase layer on top...

  3. Barium iodide and strontium iodide crystals andd scintillators implementing the same

    Science.gov (United States)

    Payne, Stephen A; Cherepy, Nerine J; Hull, Giulia E; Drobshoff, Alexander D; Burger, Arnold

    2013-11-12

    In one embodiment, a material comprises a crystal comprising strontium iodide providing at least 50,000 photons per MeV. A scintillator radiation detector according to another embodiment includes a scintillator optic comprising europium-doped strontium iodide providing at least 50,000 photons per MeV. A scintillator radiation detector in yet another embodiment includes a scintillator optic comprising SrI.sub.2 and BaI.sub.2, wherein a ratio of SrI.sub.2 to BaI.sub.2 is in a range of between 0:1 A method for manufacturing a crystal suitable for use in a scintillator includes mixing strontium iodide-containing crystals with a source of Eu.sup.2+, heating the mixture above a melting point of the strontium iodide-containing crystals, and cooling the heated mixture near the seed crystal for growing a crystal. Additional materials, systems, and methods are presented.

  4. Potassium iodide capsule treatment of feline sporotrichosis.

    Science.gov (United States)

    Reis, Erica G; Gremião, Isabella D F; Kitada, Amanda A B; Rocha, Raphael F D B; Castro, Verônica S P; Barros, Mônica B L; Menezes, Rodrigo C; Pereira, Sandro A; Schubach, Tânia M P

    2012-06-01

    Sporotrichosis is a mycosis caused by Sporothrix schenckii. The most affected animal is the cat; it has played an important role in the zoonotic transmission of this disease, especially in Rio de Janeiro, Brazil, since 1998. In order to evaluate the treatment of feline sporotrichosis with potassium iodide, an observational cohort was conducted in 48 cats with sporotrichosis at Instituto de Pesquisa Clínica Evandro Chagas, Fiocruz. All cats received potassium iodide capsules, 2.5 mg/kg to 20 mg/kg q24h. The cure rate was 47.9%, treatment failure was 37.5%, treatment abandonment was 10.4% and death was 4.2%. Clinical adverse effects were observed in 52.1% of the cases. Thirteen cats had a mild increase in hepatic transaminase levels during the treatment, six of them presented clinical signs suggestive of hepatotoxicity. Compared to previous studies with itraconazole and iodide in saturated solution, potassium iodide capsules are an alternative for feline sporotrichosis treatment.

  5. Chlorine dioxide and hemodialysis

    Energy Technology Data Exchange (ETDEWEB)

    Smith, R.P. (Dartmouth Coll., Hanover, NH (USA). Dept. of Pharmacology and Toxicology)

    1989-05-01

    Because it has little or no tendency to generate carcinogenic trihalomethanes such as chloroform, chlorine dioxide is an attractive alternative to chlorine for drinking water disinfection. There are, however, concerns about its acute toxicity, and the toxic effects of its by-products, chlorite and chlorate. The human experience with chlorine dioxide in both controlled, prospective studies and in actual use situations in community water supplies have as yet failed to reveal adverse health effects. The EPA has recommended standards of 0.06 mg/L for chlorine dioxide and standards of 0.007 mg/L for chlorite and chlorate in drinking water. Among groups who may be at special risk from oxychlorines in drinking water are patients who must undergro chronic extracorporeal hemodialysis. Although even units for home hemodialysis are supposed to be equipped with devices which effectively remove oxychlorines, there is a always a possibility of operator error or equipment failure. When the equipment is adequately maintained, it is likely that dialysis patients will have more intensive exposures from drinking water than from dialysis fluids despite the much larger volumes of water that are involved in dialysis. This paper discusses a hemodialysis and the standards and effects of oxychlorines. 90 refs., 2 tabs.

  6. Atomic force microscopy of lead iodide crystal surfaces

    Science.gov (United States)

    George, M. A.; Azoulay, M.; Jayatirtha, H. N.; Biao, Y.; Burger, A.; Collins, W. E.; Silberman, E.

    1994-03-01

    Atomic force microscopy (AFM) was used to characterize the surface of lead iodide crystals. The high vapor pressure of lead iodide prohibits the use of traditional high resolution surface study techniques that require high vacuum conditions. AFM was used to image numerous insulating surface in various ambients, with very little sample preparation techniques needed. Freshly cleaved and modified surfaces, including, chemical and vacuum etched, and air aged surfaces, were examined. Both intrinsic and induced defects were imaged with high resolution. The results were compared to a similar AFM study of mercuric iodide surfaces and it was found that, at ambient conditions, lead iodide is significantly more stable than mercuric iodide.

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

    OpenAIRE

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

    1986-01-01

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

  8. Formulation and optimization of potassium iodide tablets

    OpenAIRE

    Al-Achi, Antoine; Patel, Binit

    2014-01-01

    The use of potassium iodide (KI) as a protective agent against accidental radioactive exposure is well established. In this study, we aimed to prepare a KI tablet formulation using a direct compression method. We utilized Design of Experiment (DoE)/mixture design to define the best formulation with predetermined physical qualities as to its dissolution, hardness, assay, disintegration, and angle of repose. Based on the results from the DoE, the formulation had the following components (%w/w):...

  9. Formulation and optimization of potassium iodide tablets.

    Science.gov (United States)

    Al-Achi, Antoine; Patel, Binit

    2015-01-01

    The use of potassium iodide (KI) as a protective agent against accidental radioactive exposure is well established. In this study, we aimed to prepare a KI tablet formulation using a direct compression method. We utilized Design of Experiment (DoE)/mixture design to define the best formulation with predetermined physical qualities as to its dissolution, hardness, assay, disintegration, and angle of repose. Based on the results from the DoE, the formulation had the following components (%w/w): Avicel 48.70%, silicon dioxide 0.27%, stearic acid (1.00%), magnesium stearate 2.45%, and dicalcium phosphate 18.69%, in addition to potassium iodide 28.89% (130 mg/tablet). This formulation was scaled-up using two tablet presses, a single-punch press and a rotary mini tablet press. The final scaled-up formulation was subjected to a variety of quality control tests, including photo-stability testing. The results indicate that potassium iodide tablets prepared by a rotary mini tablet press had good pharmaceutical characteristics and a shelf-life of 25 days when stored at room temperature protected from light.

  10. Formation of cyanogen iodide by lactoperoxidase.

    Science.gov (United States)

    Schlorke, Denise; Flemmig, Jörg; Birkemeyer, Claudia; Arnhold, Jürgen

    2016-01-01

    The haem protein lactoperoxidase (LPO) is an important component of the anti-microbial immune defence in external secretions and is also applied as preservative in food, oral care and cosmetic products. Upon oxidation of SCN(-) and I(-) by the LPO-hydrogen peroxide system, oxidised species are formed with bacteriostatic and/or bactericidal activity. Here we describe the formation of the inter(pseudo)halogen cyanogen iodide (ICN) by LPO. This product is formed when both, thiocyanate and iodide, are present together in the reaction mixture. Using (13)C nuclear magnetic resonance spectroscopy and gas chromatography-mass spectrometry we could identify this inter(pseudo)halogen after applying iodide in slight excess over thiocyanate. The formation of ICN is based on the reaction of oxidised iodine species with thiocyanate. Further, we could demonstrate that ICN is also formed by the related haem enzyme myeloperoxidase and, in lower amounts, in the enzyme-free system. As I(-) is not competitive for SCN(-) under physiologically relevant conditions, the formation of ICN is not expected in secretions but may be relevant for LPO-containing products.

  11. A comparison of chlorinated organic material produced by chlorine and chlorine dioxide bleaching

    Energy Technology Data Exchange (ETDEWEB)

    McKaque, A.B.; Reeve, D.W. [Univ. of Toronto (Canada)

    1995-12-31

    Chlorine and chlorine dioxide react differently with pulp during bleaching and produce different types of organic by-products. The main differences are the large reduction in the amount of AOX (adsorbable organic halogen) in the effluent and EOX (extractable organic halogen) in the pulp. This talk reviews the differences in the amounts and types of chlorinated organic by-products produced by the two different bleaching agents.

  12. Cu-catalyzed trifluoromethylation of aryl iodides with trifluoromethylzinc reagent prepared in situ from trifluoromethyl iodide

    Directory of Open Access Journals (Sweden)

    Yuzo Nakamura

    2013-11-01

    Full Text Available The trifluoromethylation of aryl iodides catalyzed by copper(I salt with trifluoromethylzinc reagent prepared in situ from trifluoromethyl iodide and Zn dust was accomplished. The catalytic reactions proceeded under mild reaction conditions, providing the corresponding aromatic trifluoromethylated products in moderate to high yields. The advantage of this method is that additives such as metal fluoride (MF, which are indispensable to activate silyl groups for transmetallation in the corresponding reactions catalyzed by copper salt by using the Ruppert–Prakash reagents (CF3SiR3, are not required.

  13. Chlorine, Chloramine, Chlorine Dioxide, and Ozone Susceptibility of Mycobacterium avium

    Science.gov (United States)

    Taylor, Robert H.; Falkinham, Joseph O.; Norton, Cheryl D.; LeChevallier, Mark W.

    2000-01-01

    Environmental and patient isolates of Mycobacterium avium were resistant to chlorine, monochloramine, chlorine dioxide, and ozone. For chlorine, the product of the disinfectant concentration (in parts per million) and the time (in minutes) to 99.9% inactivation for five M. avium strains ranged from 51 to 204. Chlorine susceptibility of cells was the same in washed cultures containing aggregates and in reduced aggregate fractions lacking aggregates. Cells of the more slowly growing strains were more resistant to chlorine than were cells of the more rapidly growing strains. Water-grown cells were 10-fold more resistant than medium-grown cells. Disinfectant resistance may be one factor promoting the persistence of M. avium in drinking water. PMID:10742264

  14. Vapor Growth of Mercuric Iodide Tetragonal Prismatic Crystals

    Science.gov (United States)

    2013-03-01

    These steps were followed by immersion in 1% potassium iodide (KI) solution. The apparatus were then cleaned and rinsed thoroughly with deionized (DI...Pergamon Press, 1973. [34] N. Lyakh, “Composition and kinetic characteristics of vapour phase during mercuric iodide growing,” Crystal Res. Technol...DTRA-TR-13-6 Vapor Growth of Mercuric Iodide Tetragonal Prismatic Crystals Approved for public release, distribution is unlimited. March 2013

  15. Effect of nitrogen and oxygen on radiolysis of iodide solution

    Energy Technology Data Exchange (ETDEWEB)

    Karasawa, H.; Endo, M. [Hitachi Ltd., Power and Industrial System R+D Divisions, Ibaraki (Japan)

    1996-12-01

    The effect of nitrogen and oxygen on radiolysis of iodide solution was examined. Direct decomposition of nitrogen by {gamma}-radiation produced nitric acid to decrease a water pH. This resulted in the iodine formation in the radiolysis of iodide solution. Hydrogen peroxide was produced by the radiolysis of water containing oxygen. This worked a reducing agent to suppress the formation of iodine in the radiolysis of iodide solution. In the analytical model, fourteen iodine species were considered and reaction scheme consisted in 124 reactions. The analytical model could estimate the oxidation state of iodide ions. (author) 4 figs., 4 refs.

  16. Mercuric Iodide Anticoincidence Shield for Gamma-Ray Spectrometer Project

    Data.gov (United States)

    National Aeronautics and Space Administration — We propose to utilize a new detector material, polycrystalline mercuric iodide, for background suppression by active anticoincidence shielding in gamma-ray...

  17. Mercuric Iodide Anticoincidence Shield for Gamma-Ray Spectrometer Project

    Data.gov (United States)

    National Aeronautics and Space Administration — We utilize a new detector material, polycrystalline mercuric iodide, for background suppression by active anticoincidence shielding in gamma-ray spectrometers. Two...

  18. The addition of iodine to tetramethylammonium iodide

    Science.gov (United States)

    Foote, H.W.; Fleischer, M.

    1953-01-01

    The system tetramethylammonium iodide-iodine-toluene has been studied by the solubility method at 6 and at 25??. The compounds (CH3)4NI3, (CH3)4NI5 and (CH3)4NI11 were found to be stable phases at both temperatures. In addition, the compound (CH3)4NI10 was found at 6?? and the compound (CH3)4NI9 at 25??. The dissociation pressures of the compounds at these temperatures were calculated from the solubility data.

  19. Electronic and optical properties of lead iodide

    DEFF Research Database (Denmark)

    Ahuja, R.; Arwin, H.; Ferreira da Silva, A.

    2002-01-01

    The electronic properties and the optical absorption of lead iodide (PbI2) have been investigated experimentally by means of optical absorption and spectroscopic ellipsometry, and theoretically by a full-potential linear muffin-tin-orbital method. PbI2 has been recognized as a very promising...... detector material with a large technological applicability. Its band-gap energy as a function of temperature has also been measured by optical absorption. The temperature dependence has been fitted by two different relations, and a discussion of these fittings is given. ©2002 American Institute of Physics....

  20. Novel mercuric iodide polycrystalline nuclear particles counters

    Energy Technology Data Exchange (ETDEWEB)

    Schieber, M. [Hebrew Univ. of Jerusalem (Israel)]|[Sandia National Lab., Livermore, CA (United States); Zuck, A.; Braiman, M.; Nissenbaum, J. [Hebrew Univ. of Jerusalem (Israel)] [and others

    1996-12-31

    Polycrystalline mercuric iodide nuclear radiation detectors having areas between 0.01 to 100 cm{sup 2} and thicknesses 30 to 600 microns, have been fabricated with single, linear strip and square pixel contact. The large area detectors 10 to 600 cm{sup 2} were produced by industrial ceramic equipment while the smaller ones, about 1 cm{sup 2} area, were produced in the laboratory. The large detectors still had large leakage currents and the production process is being revised. The smaller detectors were tested and their response to lower and higher gamma energy, beta and even 100 GeV muons at CERN will be reported.

  1. Production of Molecular Iodine and Tri-iodide in the Frozen Solution of Iodide: Implication for Polar Atmosphere.

    Science.gov (United States)

    Kim, Kitae; Yabushita, Akihiro; Okumura, Masanori; Saiz-Lopez, Alfonso; Cuevas, Carlos A; Blaszczak-Boxe, Christopher S; Min, Dae Wi; Yoon, Ho-Il; Choi, Wonyong

    2016-02-01

    The chemistry of reactive halogens in the polar atmosphere plays important roles in ozone and mercury depletion events, oxidizing capacity, and dimethylsulfide oxidation to form cloud-condensation nuclei. Among halogen species, the sources and emission mechanisms of inorganic iodine compounds in the polar boundary layer remain unknown. Here, we demonstrate that the production of tri-iodide (I3(-)) via iodide oxidation, which is negligible in aqueous solution, is significantly accelerated in frozen solution, both in the presence and the absence of solar irradiation. Field experiments carried out in the Antarctic region (King George Island, 62°13'S, 58°47'W) also showed that the generation of tri-iodide via solar photo-oxidation was enhanced when iodide was added to various ice media. The emission of gaseous I2 from the irradiated frozen solution of iodide to the gas phase was detected by using cavity ring-down spectroscopy, which was observed both in the frozen state at 253 K and after thawing the ice at 298 K. The accelerated (photo-)oxidation of iodide and the subsequent formation of tri-iodide and I2 in ice appear to be related with the freeze concentration of iodide and dissolved O2 trapped in the ice crystal grain boundaries. We propose that an accelerated abiotic transformation of iodide to gaseous I2 in ice media provides a previously unrecognized formation pathway of active iodine species in the polar atmosphere.

  2. Inactivation of Chironomid Larvae with Chlorine Dioxide and Chlorine

    Institute of Scientific and Technical Information of China (English)

    SUN Xin-bin; CUI Fu-yi

    2008-01-01

    Chironomid larvae propagate prolifically in eutrophic water body and they cannot be exterminated by conventional disinfection process.The inactivation effects of chlorine and chlorine dioxide on Chironomid larvae were investigated and some boundary values in practice were determined under conditions of various oxidant dosage,organic precursor concentration and pH value.In addition,removal effect of differmt pre-oxidation combined with coagulation process on Chironomid larvae in law water was evaluated.It was found that chlorine dioxide possessed better inactivation effect than chlorine.Complete inactivation of Chironomid larvae in raw water was resulted by 1.5mg/L of chlorine dioxide with 30min of contact time. Additionally,the ocgallic precursor concentration,pH value had little influence on the inactivation effect.The coagulation jar test showed that Chironomid larvae in the raw water could be completely ronxwed by chlorine dioxide pre-oxidation in combination with the omgulation process at chlorine dioxide dosage of 0.8 mg/L.

  3. Phase 2 Methyl Iodide Deep-Bed Adsorption Tests

    Energy Technology Data Exchange (ETDEWEB)

    Soelberg, Nick [Idaho National Lab. (INL), Idaho Falls, ID (United States); Watson, Tony [Idaho National Lab. (INL), Idaho Falls, ID (United States)

    2014-09-01

    Nuclear fission produces fission products (FPs) and activation products, including iodine-129, which could evolve into used fuel reprocessing facility off-gas systems, and could require off-gas control to limit air emissions to levels within acceptable emission limits. Research, demonstrations, and some reprocessing plant experience have indicated that diatomic iodine can be captured with efficiencies high enough to meet regulatory requirements. Research on the capture of organic iodides has also been performed, but to a lesser extent. Several questions remain open regarding the capture of iodine bound in organic compounds. Deep-bed methyl iodide adsorption testing has progressed according to a multi-laboratory methyl iodide adsorption test plan. This report summarizes the second phase of methyl iodide adsorption work performed according to this test plan using the deep-bed iodine adsorption test system at the Idaho National Laboratory (INL), performed during the second half of Fiscal Year (FY) 2014. Test results continue to show that methyl iodide adsorption using AgZ can achieve total iodine decontamination factors (DFs, ratios of uncontrolled and controlled total iodine levels) above 1,000, until breakthrough occurred. However, mass transfer zone depths are deeper for methyl iodide adsorption compared to diatomic iodine (I2) adsorption. Methyl iodide DFs for the Ag Aerogel test adsorption efficiencies were less than 1,000, and the methyl iodide mass transfer zone depth exceeded 8 inches. Additional deep-bed testing and analyses are recommended to (a) expand the data base for methyl iodide adsorption under various conditions specified in the methyl iodide test plan, and (b) provide more data for evaluating organic iodide reactions and reaction byproducts for different potential adsorption conditions.

  4. Kinetic Isotope Effects in the Reduction of Methyl Iodide

    DEFF Research Database (Denmark)

    Holm, Torkil

    1999-01-01

    a-Deuterium kinetic isotope effects (KIE's) have been determined for the reaction of methyl iodide with a series of reducing agents. Reagents which transfer hydride ion in an SN2 reaction show small inverse or small normal KIE's. Reagents which transfer an electron to methyl iodide to produce...

  5. Gaseous, chlorine-free chlorine dioxide for drinking water

    Energy Technology Data Exchange (ETDEWEB)

    Gordon, G. [Miami Univ., Oxford, OH (United States); Rosenblatt, A. [CDG Technology Inc., New York, NY (United States)

    1996-11-01

    The benefits of applying chlorine dioxide (ClO{sub 2}) for the oxidative treatment of drinking water are well established. Chlorine dioxide treated finished water typically has substantially lower trihalomethane (THM) levels because ClO{sub 2} will not form chlorinated organic species as a by-product of disinfection. The THMs that are formed are probably due to chlorine from the generator or chlorine used to maintain a post-disinfection residual. An emerging regulatory issue concerning the formation of disinfection by-products (DBPs) is causing the water industry to set standards for the generation and delivery of ClO{sub 2}. The Federal Register (11 February 1994) contains language developed to limit the production of the unwanted inorganic by-products chlorite (ClO{sub 2}{sup -}), chlorate (ClO{sub 3}{sup -}), and bromate (BrO{sub 3}{sup -}) ions by requiring utilities to maintain high (95%) generation efficiencies and by limiting the amount of excess Cl{sub 2} that can be used during the generation process. The efficiency and excess Cl{sub 2} regulations may be problematic for utilities that over-chlorinate to attain chlorine dioxide high yields. Many utilities will have to decide either to reduce the amount of Cl{sub 2} used to react with sodium chlorite (NaClO{sub 2}), thereby increasing the ClO{sub 2}{sup -} residual in finished water, or over-chlorinate to increase yields and surpass the excess Cl{sub 2} limits.

  6. Improved method generates more chlorine dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Jordan, R.W.; Kosinski, A.J.; Baker, R.J.

    1980-10-01

    The addition of acid can greatly improve the chlorine-chlorite process and enhance the use of chlorine dioxide as an alternative to chlorine for disinfection. The process is economical for use in taste and odor control, and for manganese, oxidation. The maximum yield is obtained using no excess chlorine, and the amount of unreacted sodium chlorite and chlorine in the product stream is reduced. (1 diagram, 4 graphs, 9 references)

  7. Grundfoss: Chlorination of Swimming Pools

    DEFF Research Database (Denmark)

    Hjorth, Poul G.; Hogan, John; Andreassen, Viggo

    1998-01-01

    Grundfos asked for a model, describing the problem of mixing chemicals, being dosed into water systems, to be developed. The application of the model should be dedicated to dosing aqueous solution of chlorine into swimming pools.......Grundfos asked for a model, describing the problem of mixing chemicals, being dosed into water systems, to be developed. The application of the model should be dedicated to dosing aqueous solution of chlorine into swimming pools....

  8. Silver iodide sodalite for 129I immobilisation

    Science.gov (United States)

    Vance, E. R.; Gregg, D. J.; Grant, C.; Stopic, A.; Maddrell, E. R.

    2016-11-01

    Silver iodide sodalite was initially synthesised as a fine-grained major phase in a nominally stoichiometric composition following hot isostatic pressing at 850 °C with 100 MPa and its composition, Ag4Al3Si3O12I, was approximately verified by scanning electron microscopy. An alternative preparative method yielded a more dense and stoichiometric AgI sodalite on sintering and HIPing. As found for AgI, the I is released from AgI sodalite much more readily in reducing water than in ordinary water. Thus in normal PCT-B tests, the I release was <0.3 g/L in water, but it was ∼70 g/L under highly reducing conditions. This is an important point with regard to can material if HIPing is used for consolidation.

  9. Novel mercuric iodide polycrystalline nuclear particle counters

    Energy Technology Data Exchange (ETDEWEB)

    Schieber, M. [Hebrew Univ. of Jerusalem (Israel)]|[Sandia National Labs., Livermore, CA (United States); Zuck, A.; Braiman, M.; Nissenbaum, J. [Hebrew Univ. of Jerusalem (Israel); Turchetta, R.; Dulinski, W.; Husson, D.; Riester, J.L. [LEPSI, Strasbourg (France)

    1997-12-01

    Polycrystalline mercuric iodide nuclear radiation detectors have been produced in a novel technology. Unlike the normal single-crystal technology, there is no intrinsic limit to the surface on which these detectors can be produced. Detectors with areas up to about 1.5 cm{sup 2}, thicknesses from 30 to 600 {micro}m, and with single electrodes as well as microstrip and pixel contacts have been fabricated and successfully tested with photons in the range of 40--660 keV, {beta} particle`s emitted from a Sr-Y source, and high energy (100 GeV) muons. Results on both charge collection and counting efficiency are reported as well as some very preliminary imaging results. The experimental results on charge collection have been compared with simulation, and a combined {mu}{tau} product 10{sup {minus}7} cm{sup 2}/V for electrons has been estimated.

  10. Ferroelastic Fingerprints in Methylammonium Lead Iodide Perovskite

    KAUST Repository

    Hermes, Ilka M.

    2016-02-12

    Methylammonium lead iodide (MAPbI3) perovskite materials show an outstanding performance in photovoltaic devices. However, certain material properties, especially the possible ferroic behavior, remain unclear. We observed distinct nanoscale periodic domains in the piezoresponse of MAPbI3(Cl) grains. The structure and the orientation of these striped domains indicate ferroelasticity as their origin. By correlating vertical and lateral piezoresponse force microscopy experiments performed at different sample orientations with x-ray diffraction, the preferred domain orientation was suggested to be the a1-a2-phase. The observation of these ferroelastic fingerprints appears to strongly depend on the film texture and thus the preparation route. The formation of the ferroelastic twin domains could be induced by internal strain during the cubic-tetragonal phase transition.

  11. Conserved charged amino acid residues in the extracellular region of sodium/iodide symporter are critical for iodide transport activity

    Directory of Open Access Journals (Sweden)

    Liang Ji-An

    2010-11-01

    Full Text Available Abstract Background Sodium/iodide symporter (NIS mediates the active transport and accumulation of iodide from the blood into the thyroid gland. His-226 located in the extracellular region of NIS has been demonstrated to be critical for iodide transport in our previous study. The conserved charged amino acid residues in the extracellular region of NIS were therefore characterized in this study. Methods Fourteen charged residues (Arg-9, Glu-79, Arg-82, Lys-86, Asp-163, His-226, Arg-228, Asp-233, Asp-237, Arg-239, Arg-241, Asp-311, Asp-322, and Asp-331 were replaced by alanine. Iodide uptake abilities of mutants were evaluated by steady-state and kinetic analysis. The three-dimensional comparative protein structure of NIS was further modeled using sodium/glucose transporter as the reference protein. Results All the NIS mutants were expressed normally in the cells and targeted correctly to the plasma membrane. However, these mutants, except R9A, displayed severe defects on the iodide uptake. Further kinetic analysis revealed that mutations at conserved positively charged amino acid residues in the extracellular region of NIS led to decrease NIS-mediated iodide uptake activity by reducing the maximal rate of iodide transport, while mutations at conserved negatively charged residues led to decrease iodide transport by increasing dissociation between NIS mutants and iodide. Conclusions This is the first report characterizing thoroughly the functional significance of conserved charged amino acid residues in the extracellular region of NIS. Our data suggested that conserved charged amino acid residues, except Arg-9, in the extracellular region of NIS were critical for iodide transport.

  12. Transformation of iopamidol during chlorination.

    Science.gov (United States)

    Wendel, Friedrich M; Lütke Eversloh, Christian; Machek, Edward J; Duirk, Stephen E; Plewa, Michael J; Richardson, Susan D; Ternes, Thomas A

    2014-11-01

    The transformation of the iodinated X-ray contrast media (ICM) iopamidol, iopromide, iohexol, iomeprol, and diatrizoate was examined in purified water over the pH range from 6.5 to 8.5 in the presence of sodium hypochlorite, monochloramine, and chlorine dioxide. In the presence of aqueous chlorine, only iopamidol was transformed. All other ICM did not show significant reactivity, regardless of the oxidant used. Chlorination of iopamidol followed a second order reaction, with an observed rate constant of up to 0.87 M(-1) s(-1) (±0.021 M(-1) s(-1)) at pH 8.5. The hypochlorite anion was identified to be the reactive chlorine species. Iodine was released during the transformation of iopamidol, and was mainly oxidized to iodate. Only a small percentage (less than 2% after 24 h) was transformed to known organic iodinated disinfection byproducts (DBPs) of low molecular weight. Some of the iodine was still present in high-molecular weight DBPs. The chemical structures of these DBPs were elucidated via MSn fragmentation and NMR. Side chain cleavage was observed as well as the exchange of iodine by chlorine. An overall transformation pathway was proposed for the degradation of iopamidol. CHO cell chronic cytotoxicity tests indicate that chlorination of iopamidol generates a toxic mixture of high molecular weight DBPs (LC50 332 ng/μL).

  13. Barium iodide and strontium iodide crystals and scintillators implementing the same

    Energy Technology Data Exchange (ETDEWEB)

    Payne, Stephen A.; Cherepy, Nerine J.; Hull, Giulia E.; Drobshoff, Alexander D.; Burger, Arnold

    2016-11-29

    In one embodiment, a material comprises a crystal comprising strontium iodide providing at least 50,000 photons per MeV, where the strontium iodide material is characterized by a volume not less than 1 cm.sup.3. In another embodiment, a scintillator optic includes europium-doped strontium iodide providing at least 50,000 photons per MeV, where the europium in the crystal is primarily Eu.sup.2+, and the europium is present in an amount greater than about 1.6%. A scintillator radiation detector in yet another embodiment includes a scintillator optic comprising SrI.sub.2 and BaI.sub.2, where a ratio of SrI.sub.2 to BaI.sub.2 is in a range of between 0:1 and 1.0, the scintillator optic is a crystal that provides at least 50,000 scintillation photons per MeV and energy resolution of less than about 5% at 662 keV, and the crystal has a volume of 1 cm.sup.3 or more; the scintillator optic contains more than about 2% europium.

  14. Cleaning without chlorinated solvents

    Energy Technology Data Exchange (ETDEWEB)

    Thompson, L.M.; Simandl, R.F.

    1994-12-31

    Because of health and environmental concerns, many regulations have been passed in recent years regarding the use of chlorinated solvents. The Oak Ridge Y-12 Plant has had an active program to find alternatives for these solvents used in cleaning applications for the past 7 years. During this time frame, the quantity of solvents purchased has been reduced by 92%. The program has been a twofold effort. Vapor degreasers used in batch cleaning-operations have been replaced by ultrasonic cleaning with aqueous detergent, and other organic solvents have been identified for use in hand-wiping or specialty operations. In order to qualify these alternatives for use, experimentation was conducted on cleaning ability as well as effects on subsequent operations such as welding, painting and bonding. Cleaning ability was determined using techniques such as X-ray photoelectron spectroscopy (XPS) and Fourier Transform Infrared Spectroscopy (FTIR) which are capable of examining monolayer levels of contamination on a surface. Solvents have been identified for removal of rust preventative oils, lapping oils, machining coolants, lubricants, greases, and mold releases. Solvents have also been evaluated for cleaning urethane foam spray guns, swelling of urethanes and swelling of epoxies.

  15. Expression of the human sodium/iodide symporter (hNIS) in xenotransplanted human thyroid carcinoma

    NARCIS (Netherlands)

    Smit, J.W.A.; Schröder - van der Elst, J.P.; Karperien, M.; Que, I.; Romijn, J.A.; Heide, van der D.

    2001-01-01

    The uptake of iodide in thyroid epithelial cells is mediated by the sodium/iodide symporter (NIS). The uptake of iodide is of vital importance for thyroid physiology and is a prerequisite for radioiodine therapy in thyroid cancer. Loss of iodide uptake due to diminished expression of the human NIS (

  16. Improved Stability of Mercuric Iodide Detectors for Anticoincidence Shields Project

    Data.gov (United States)

    National Aeronautics and Space Administration — We propose to utilize guard ring electrode structures and a new film growth technique to create improved polycrystalline mercuric iodide detectors for background...

  17. Prevention of organic iodide formation in BWR`s

    Energy Technology Data Exchange (ETDEWEB)

    Karjunen, T. [Finnish Centre for Radiation and Nuclear Safety, Helsinki (Finland); Laitinen, T.; Piippo, J.; Sirkiae, P. [VTT Manufacturing Technology (Finland)

    1996-12-01

    During an accident, many different forms of iodine may emerge. Organic iodides, such as methyl iodide and ethyl iodide, are relatively volatile, and thus their appearance leads to increased concentration of gaseous iodine. Since organic iodides are also relatively immune to most accident mitigation measures, such as sprays and filters, they can affect the accident source term significantly even when only a small portion of iodine is in organic form. Formation of organic iodides may not be limited by the amount of organic substances available. Excessive amounts of methane can be produced, for example, during oxidation of boron carbide, which is used in BWR`s as a neutron absorber material. Another important source is cable insulation. In a BWR, a large quantity of cables is placed below the pressure vessel. Thus a large quantity of pyrolyse gases will be produced, should the vessel fail. Organic iodides can be formed as a result of many different reactions, but at least in certain conditions the main reaction takes place between an organic radical produced by radiolysis and elemental iodine. A necessary requirement for prevention of organic iodide production is therefore that the pH in the containment water pools is kept high enough to eliminate formation of elemental iodine. In a typical BWR the suppression pool water is usually unbuffered. As a result, the pH may be dominated by chemicals introduced during an accident. If no system for adding basic chemicals is operable, the main factor affecting pool water pH may be hydrochloric acid released during cable degradation. Should this occur, the conditions could be very favorable for production of elemental iodine and, consequently, formation of organic iodides. Although high pH is necessary for iodine retention, it could have also adverse effects. High pH may, for example, accelerate corrosion of containment materials and alter the characteristics of the solid corrosion products. (author) 6 figs., 1 tab., 13 refs.

  18. Chloride, bromide and iodide scintillators with europium

    Science.gov (United States)

    Zhuravleva, Mariya; Yang, Kan

    2016-09-27

    A halide scintillator material is disclosed where the halide may comprise chloride, bromide or iodide. The material is single-crystalline and has a composition of the general formula ABX.sub.3 where A is an alkali, B is an alkali earth and X is a halide which general composition was investigated. In particular, crystals of the formula ACa.sub.1-yEu.sub.yI.sub.3 where A=K, Rb and Cs were formed as well as crystals of the formula CsA.sub.1-yEu.sub.yX.sub.3 (where A=Ca, Sr, Ba, or a combination thereof and X=Cl, Br or I or a combination thereof) with divalent Europium doping where 0.ltoreq.y.ltoreq.1, and more particularly Eu doping has been studied at one to ten mol %. The disclosed scintillator materials are suitable for making scintillation detectors used in applications such as medical imaging and homeland security.

  19. Electrochemical reaction rates in a dye-sensitised solar cell - the iodide/tri-iodide redox system

    DEFF Research Database (Denmark)

    Bay, L.; West, K.; Winther-Jensen, B.

    2006-01-01

    The electrochemical reaction rate of the redox couple iodide/tri-iodide in acetonitrile is characterised by impedance spectroscopy. Different electrode materials relevant for the function of dye-sensitised solar cells (DSSC) are investigated. Preferably, the reaction with the iodide....../tri-iodide couple should be fast at the counter electrode, i.e. this electrode must have a high catalytic activity towards the redox couple, and the same reaction must be slow on the photo electrode. The catalytic activity is investigated for platinum, poly(3,4-ethylenedioxythiophene) (PEDOT), polypyrrole (PPy......), and polyaniline (PANI)-all deposited onto fluorine-doped tin oxide (FTO) glass. Both Pt and PEDOT are found to have sufficiently high catalytic activities for practical use as counter electrodes in DSSC. The reaction resistance on FTO and anatase confirmed the beneficial effect of a compact anatase layer on top...

  20. Colorectal cancers and chlorinated water

    Institute of Scientific and Technical Information of China (English)

    Ahmed Mahmoud El-Tawil

    2016-01-01

    Published reports have revealed increased risk of colorectal cancers in people exposed to chlorinated drinking water or chemical derivatives of chlorination. Oestrogen plays a dual positive functions for diminishing the possibilities of such risk by reducing the entrance, and increasing the excretion, of these chemicals. In addition, there are supplementary measures that could be employed in order to reduce this risk further, such as boiling the drinking water, revising the standard concentrations of calcium, magnesium and iron in the public drinking water and prescribing oestrogen in susceptible individuals. Hypo-methylation of genomic DNA could be used as a biological marker for screening for the potential development of colorectal cancers.

  1. Effects of ozone, chlorine dioxide, chlorine, and monochloramine on Cryptosporidium parvum oocyst viability.

    OpenAIRE

    Korich, D. G.; Mead, J R; Madore, M S; Sinclair, N A; Sterling, C R

    1990-01-01

    Purified Cryptosporidium parvum oocysts were exposed to ozone, chlorine dioxide, chlorine, and monochloramine. Excystation and mouse infectivity were comparatively evaluated to assess oocyst viability. Ozone and chlorine dioxide more effectively inactivated oocysts than chlorine and monochloramine did. Greater than 90% inactivation as measured by infectivity was achieved by treating oocysts with 1 ppm of ozone (1 mg/liter) for 5 min. Exposure to 1.3 ppm of chlorine dioxide yielded 90% inactiv...

  2. Disinfectants: Chlorine and chlorine dioxide. (Latest citations from the Life Sciences Collection database). Published Search

    Energy Technology Data Exchange (ETDEWEB)

    1993-05-01

    The bibliography contains citations concerning the antimicrobial properties of chlorine and chlorine dioxide. The use of chlorine for the inactivation of viruses, bacteria, and fungi in wastewater treatment plants is discussed, including the mode of action and factors influencing inactivation. The use of chlorine dioxide as an alternative to chlorine disinfection in swimming pools and water supplies, and possible adverse effects are also discussed. (Contains a minimum of 157 citations and includes a subject term index and title list.)

  3. Iodide kinetics and experimental I-131 therapy in a xenotransplanted human sodium-iodide symporter-transfected human follicular thyroid carcinoma cell line

    NARCIS (Netherlands)

    Smit, J.W.A.; Elst, van der J.P.; Karperien, M.; Que, I.; Stokkel, M.; Heide, van der D.; Romijn, J.A.

    2002-01-01

    Uptake of iodide is a prerequisite for radioiodide therapy in thyroid cancer. However, loss of iodide uptake is frequently observed in metastasized thyroid cancer, which may be explained by diminished expression of the human sodium-iodide symporter (hNIS). We studied whether transfection of hNIS int

  4. Molecular imaging using sodium iodide symporter (NIS)

    Energy Technology Data Exchange (ETDEWEB)

    Cho, Je Yoel [School of Dentistry, Kyungpook National Univ., Daegu (Korea, Republic of)

    2004-04-01

    Radioiodide uptake in thyroid follicular epithelial cells, mediated by a plasma membrane transporter, sodium iodide symporter (NIS), provides a first step mechanism for thyroid cancer detection by radioiodide injection and effective radioiodide treatment for patients with invasive, recurrent, and/or metastatic thyroid cancers after total thyroidectomy. NIS gene transfer to tumor cells may significantly and specifically enhance internal radioactive accumulation of tumors following radioiodide administration, and result in better tumor control. NIS gene transfers have been successfully performed in a variety of tumor animal models by either plasmid-mediated transfection or virus (adenovirus or retrovirus)-mediated gene delivery. These animal models include nude mice xenografted with human melanoma, glioma, breast cancer of prostate cancer, rats with subcutaneous thyroid tumor implantation, as well as the rat intracranial glioma model. In these animal models, non-invasive imaging of in vivo tumors by gamma camera scintigraphy after radioiodide or technetium injection has been performed successfully, suggesting that the NIS can serve as an imaging reporter gene for gene therapy trials. In addition, the tumor killing effects of I-131, ReO4-188 and At-211 after NIS gene transfer have been demonstrated in in vitro clonogenic assays and in vivo radioiodide therapy studies, suggesting that NIS gene can also serve as a therapeutic requires a more efficient and specific system of gene delivery with better retention of radioiodide in tumor. Results thus far are, however, promising, and suggest that NIS gene transfer followed by radioiodide treatment will allow non-invasive in vivo imaging to assess the outcome of gene therapy and provide a therapeutic strategy for a variety of human diseases.

  5. Evaluation of mercuric iodide ceramic semiconductor detectors

    Energy Technology Data Exchange (ETDEWEB)

    Schieber, M.; Zuck, A.; Braiman, M.; Nissenbaum, J. [Hebrew Univ., Jerusalem (Israel); Turchetta, R.; Dulinski, W.; Husson, D.; Riester, J.L. [LEPSI (ULP/IN2P3), Strasbourg (France)

    1998-02-01

    Mercuric iodide ceramic radiation detectors, which can act as nuclear particle counters, have been fabricated with single continuos electrical contacts and with linear strip contacts. They have been tested with different kinds of {gamma} and {beta} sources as well as in a high energy beam at CERN. The detectors were also successfully tested for radiation hardness with irradiation of 5*10{sup 14} neutrons/cm{sup 2}. The ratio of detected photons over the number of absorbed photons has been measured with {gamma} sources of different energies, and it ranges from 20% at 44 keV up to about 30% at 660 keV. An absolute efficiency of 70% has been measured for a 350 {mu}m thick detector for {beta} particles emitted by a {sup 90}Sr source. Charge collection efficiency, defined as the amount of charge induced on the electrodes by a mminimum ionizing particle (MIP) traversing the detector, has been measured in two samples. The average collected charge fits well with a linear curve with slope of 35 electrons/(kV/cm) per 100 {mu}m. This result is well described by a dynamic device simulation, where the free carrier mean lifetime is used as a free parameter, adjusted to a value of 1.5 ns, i.e. about 1/100 of the corresponding lifetime in single crystal HgI{sub 2} detectors. The response to MIP has also been studied with a high energy (100 GeV) muon beam in CERN. A preliminary beam profile is presented while a more detailed analysis is still in progress and will be presented elsewhere. These results together with the low cost of the material make ceramic HgI{sub 2} detectors excellent candidates for large area particle tracking and imaging applications, even in a radiation harsh environment. (orig.). 14 refs.

  6. Environmental factors regulating soil organic matter chlorination

    Science.gov (United States)

    Svensson, Teresia; Montelius, Malin; Reyier, Henrik; Rietz, Karolina; Karlsson, Susanne; Lindberg, Cecilia; Andersson, Malin; Danielsson, Åsa; Bastviken, David

    2016-04-01

    Natural chlorination of organic matter is common in soils. Despite the widespread abundance of soil chlorinated soil organic matter (SOM), frequently exceeding soil chloride abundance in surface soils, and a common ability of microorganisms to produce chlorinated SOM, we lack fundamental knowledge about dominating processes and organisms responsible for the chlorination. To take one step towards resolving the terrestrial chlorine (Cl) puzzle, this study aims to analyse how environmental factors influence chlorination of SOM. Four factors were chosen for this study: soil moisture (W), nitrogen (N), chloride (Cl) and organic matter quality (C). These factors are all known to be important for soil processes. Laboratory incubations with 36Cl as a Cl tracer were performed in a two soil incubation experiments. It was found that addition of chloride and nitrogen seem to hamper the chlorination. For the C treatment, on the other hand, the results show that chlorination is enhanced by increased availability of labile organic matter (glucose and maltose). Even higher chlorination was observed when nitrogen and water were added in combination with labile organic matter. The effect that more labile organic matter strongly stimulated the chlorination rates was confirmed by the second separate experiment. These results indicate that chlorination was not primarily a way to cut refractory organic matter into digestible molecules, representing one previous hypothesis, but is related with microbial metabolism in other ways that will be further discussed in our presentation.

  7. Interactions of bromine, chlorine, and iodine photochemistry during ozone depletions in Barrow, Alaska

    Directory of Open Access Journals (Sweden)

    C. R. Thompson

    2014-11-01

    Full Text Available The springtime depletion of tropospheric ozone in the Arctic is known to be caused by active halogen photochemistry resulting from halogen atom precursors emitted from snow, ice, or aerosol surfaces. The role of bromine in driving ozone depletion events (ODEs has been generally accepted, but much less is known about the role of chlorine radicals in ozone depletion chemistry. While the potential impact of iodine in the High Arctic is more uncertain, there have been indications of active iodine chemistry through observed enhancements in filterable iodide, probable detection of tropospheric IO, and recently, detection of atmospheric I2. Despite decades of research, significant uncertainty remains regarding the chemical mechanisms associated with the bromine-catalyzed depletion of ozone, as well as the complex interactions that occur in the polar boundary layer due to halogen chemistry. To investigate this, we developed a zero-dimensional photochemical model, constrained with measurements from the 2009 OASIS field campaign in Barrow, Alaska. We simulated a 7 day period during late March that included a full ozone depletion event lasting 3 days and subsequent ozone recovery to study the interactions of halogen radicals under these different conditions. In addition, the effects of iodine added to our base model were investigated. While bromine atoms were primarily responsible for ODEs, chlorine and iodine were found to enhance the depletion rates and iodine was found to be more efficient per atom at depleting ozone than Br. The interaction between chlorine and bromine is complex, as the presence of chlorine can increase the recycling and production of Br atoms, while also increasing reactive bromine sinks under certain conditions. Chlorine chemistry was also found to have significant impacts on both HO2 and RO2. The results of this work highlight the need for future studies on the production mechanisms of Br2 and Cl2, as well as on the potential

  8. Effects of chlorine content and position of chlorinated phenols on their oxidation kinetics by potassium permanganate

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    Chlorine content and position of chlorinated phenols have many significant effects on the reactivity of oxido-reduction. The effects of chlorine content and position of chlorinated phenols on their oxidation kinetics by potassium permanganate were evaluated through different kinetics studies. Since chlorine was an electron withdrawing atom, the substitution of chlorine on the aromatic ring decreased the oxidation rate constant by σ-electron withdrawing conductive effect; at the same time, the substitution of chlorine at ortho or para position on the aromatic ring increased the oxidation rate constant by π-electron donating conjugative effect, and the conjugative effect could counteract the negative impact of the conductive effect to some extent. On the other hand, the substitution of chlorine at ortho position on the aromatic ring decreased the oxidation rate constant by steric hindrance effect. The oxidation rate constants of phenol and chlorinated phenols studied decreased as follow order: 4-chlorophenol>2,4-dichlorophenol>phenol>2,6-dichlorophenol.

  9. Macrosegregation during Plane Front Solidification of Cesium Iodide wt Percent Thallium Iodide Alloy

    Science.gov (United States)

    Sidawi, Ibrahim M. S.

    Macrosegregation produced during directional solidification of CsI-1 wt% TlI by vertical Bridgman technique has been examined in crucibles of varying diameter, from 0.5 to 2.0 cm. Phase diagram and temperature dependence of the thermal conductivity have been determined. The experimentally observed liquid-solid interface shape and the fluid flow behavior have been compared with that computed from the commercially available code FIDAP. Thallium iodide content of the alloy was observed to increase along the length of the directionally solidified specimens, resulting in continuously decreasing light output. The experimentally observed solutal distribution agrees with predictions from the boundary layer model of Favier. The observed macrosegregation behavior suggests that there is a significant convection in the melt even in the smallest crucible diameter of 0.5 cm.

  10. Bismuth tri-iodide radiation detector development

    Science.gov (United States)

    Gokhale, Sasmit S.

    Bismuth tri-iodide is an attractive material for room temperature radiation detection. BiI3 demonstrates a number of properties that are apt for semiconductor radiation detection, especially gamma ray spectroscopy. The high atomic number (ZBi = 83 and ZI = 53) and the relatively high density (5.78 g/cm3) cause the material to have good photon stopping power, while the large band-gap (1.67 eV ) allows it to function as a room temperature radiation detector without any cooling mechanism. This work presents the fabrication and characterization of BiI3 radiation detectors. For the purpose of this research detectors were fabricated by cutting BiI3 crystal boules, followed by mechanical and chemical surface treatments. Detectors with various electrode geometries enabling single polarity charge sensing were fabricated. The electrical characteristics and the radiation response of the detectors were measured. The radiation response measurement was performed at room temperature using a 241Am alpha particle source and a 241Am sealed gamma-ray source. The spectral resolutions of the detectors varied from 2.09% - 6.1% for 59.5 keV gamma-rays and between 26% - 40% for 5.48 MeV alpha particles. Charge carrier properties such as the electron and hole mobility and lifetime were also estimated. The electron mobility for an ultrapure BiI 3 detector was estimated to be approximately 433 cm 2/Vs while that for antimony doped BiI3 was estimated to be around 956 cm2/Vs and the mobility-lifetime product for electrons was estimated to be around 5.44 x 10-4 cm 2/V. Detector simulation was performed using the Monte Carlo simulation code MCNP5. A Matlab script which incorporates charge carrier trapping and statistical variation was written to generate a gamma-ray spectrum from the simulated energy deposition spectra. Measured and simulated spectra were compared to extract the charge carrier mobility-lifetime products, which for electrons and holes were estimated to be 5 x 10-3 cm2/V and 1.3 x

  11. Standard free energy of formation of iron iodide

    Science.gov (United States)

    Khandkar, A.; Tare, V. B.; Wagner, J. B., Jr.

    1983-01-01

    An experiment is reported where silver iodide is used to determine the standard free energy of formation of iron iodide. By using silver iodide as a solid electrolyte, a galvanic cell, Ag/AgI/Fe-FeI2, is formulated. The standard free energy of formation of AgI is known, and hence it is possible to estimate the standard free energy of formation of FeI2 by measuring the open-circuit emf of the above cell as a function of temperature. The free standard energy of formation of FeI2 determined by this method is -38784 + 24.165T cal/mol. It is estimated that the maximum error associated with this method is plus or minus 2500 cal/mol.

  12. Phase 1 Methyl Iodide Deep-Bed Adsorption Tests

    Energy Technology Data Exchange (ETDEWEB)

    Soelberg, Nick [Idaho National Lab. (INL), Idaho Falls, ID (United States); Watson, Tony [Idaho National Lab. (INL), Idaho Falls, ID (United States)

    2014-08-22

    Nuclear fission results in the production of fission products (FPs) and activation products including iodine-129, which could evolve into used fuel reprocessing facility off-gas systems, and could require off-gas control to limit air emissions to levels within acceptable emission limits. Research, demonstrations, and some reprocessing plant experience have indicated that diatomic iodine can be captured with efficiencies high enough to meet regulatory requirements. Research on the capture of organic iodides has also been performed, but to a lesser extent [Jubin 2012b]. Several questions remain open regarding the capture of iodine bound in organic compounds. Deep-bed methyl iodide adsorption testing has progressed according to a multi-laboratory methyl iodide adsorption test plan. This report summarizes the first phase of methyl iodide adsorption work performed according to this test plan using the deep-bed iodine adsorption test system at the Idaho National Laboratory (INL), performed during Fiscal Year (FY) 2013 and early FY-2014. Testing has been performed to address questions posed in the test plan, and followed the testing outline in the test plan. Tests established detection limits, developed procedures for sample analysis with minimal analytical interferences, and confirmed earlier results that show that the methyl iodide reacts when in contact with the AgZ sorbent, and not significantly in the gas flow upstream of the sorbent. The reaction(s) enable separation of the iodine from the organic moiety, so that the iodine can chemisorb onto the sorbent. The organic moiety can form other compounds, some of which are organic compounds that are detected and can be tentatively identified using GC-FID and GCMS. Test results also show that other gas constituents (NOx and/or H2O) can affect the methyl iodide reactions. With NOx and H2O present in the gas stream, the majority of uncaptured iodine exiting iodine-laden sorbent beds is in the form of I2 or HI, species that

  13. Chlorine signal attenuation in concrete.

    Science.gov (United States)

    Naqvi, A A; Maslehuddin, M; ur-Rehman, Khateeb; Al-Amoudi, O S B

    2015-11-01

    The intensity of prompt gamma-ray was measured at various depths from chlorine-contaminated silica fume (SF) concrete slab concrete specimens using portable neutron generator-based prompt gamma-ray setup. The intensity of 6.11MeV chloride gamma-rays was measured from the chloride contaminated slab at distance of 15.25, 20.25, 25.25, 30.25 and 35.25cm from neutron target in a SF cement concrete slab specimens. Due to attenuation of thermal neutron flux and emitted gamma-ray intensity in SF cement concrete at various depths, the measured intensity of chlorine gamma-rays decreases non-linearly with increasing depth in concrete. A good agreement was noted between the experimental results and the results of Monte Carlo simulation. This study has provided useful experimental data for evaluating the chloride contamination in the SF concrete utilizing gamma-ray attenuation method.

  14. Low energy background in mercuric iodide X-ray spectrometers

    Energy Technology Data Exchange (ETDEWEB)

    Bao, X.J. [TN Technol., Inc., Round Rock, TX (United States). Dept. of Anal. Instrum.; Natarajan, M. [TN Technol., Inc., Round Rock, TX (United States). Dept. of Anal. Instrum.; Henderson, J. [TN Technol., Inc., Round Rock, TX (United States). Dept. of Anal. Instrum.

    1996-10-01

    The origins of the continuous background (window effect or dead layer) in mercuric iodide X-ray spectrometers are investigated. It is found that photo-electron escape and carrier diffusion are the dominant mechanisms of incomplete charge collection in the energy range of interest (from 3-60 keV). X-ray spectra measurements, computer calculation and photo-response measurements are presented in support of the proposed model. Many observations of detector behavior made in the manufacturing and application of mercuric iodide X-ray detectors can be explained by this model. (orig.).

  15. DBU-Promoted Trifluoromethylation of Aryl Iodides with Difluoromethyltriphenylphosphonium Bromide

    Institute of Scientific and Technical Information of China (English)

    Yun Wei; Liuying Yu; Jinhong Lin; Xing Zheng; Jichang Xiao

    2016-01-01

    DBU-promoted trifluoromethylation of aryl iodides with difluoromethyltriphenylphosphonium bromide (DFPB) in the presence of copper source is described.In this transformation,DBU not only acts as base to deprotonate the difluoromethyl group in DFPB to generate difluoromethylene phosphonium ylide Ph3P+CF2,but also converts the difluorocarbene generated from ylide Ph3P+CF2 into trifluoromethyl anion,finally resulting in the trifluoromethylation of aryl iodides.The reactions proceeded smoothly to afford expected products in moderate to good yields.

  16. Mercuric iodide dosimeter response to high energy electron beams

    Energy Technology Data Exchange (ETDEWEB)

    Loewinger, E.; Nissenbaum, J.; Schieber, M.M.

    1988-01-01

    Mercuric iodide solid state dosimeter response to high energy electron beams of up to 35 MeV is reported. High sensitivity of up to 1.5 V/cGy was observed with a 200 V external bias, as well as several mV/cGy, with no external bias for small volume (approx. 10 mm/sup 3/) detectors. The physical characteristics of the detector response are discussed, showing the feasibility of mercuric iodide as a reliable dosimeter for high energy electron beams.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1986-11-01

    This presentation reviews published information concerning the reactions of chlorine gas (CL/sub 2/(g)), aqueous chlorine, and ClO/sub 2/ with model food compounds, the fate of chlorine during the chlorination of specific food products, and the potential toxicity of the reaction products. Fatty acids and their methyl esters react with chlorine with the degree of incorporation corresponding to their degree of unsaturation. Aqueous chlorine oxidizes and chlorinates lipids and amino acids much more readily than ClO/sub 2/. Several amino acids are highly susceptible to oxidation and chlorination by chlorine compounds. Reactions of chlorine and ClO/sub 2/ with several food products, including flour and shrimp, have also been characterized. Although significant quantities of chlorine can be incorporated into specific model compounds and food products, the health risks associated with exposure to chlorinated organic products are unknown. Preliminary studies using the Ames Salmonella/microsome mutagenicity assay indicate that the reaction products from mixtures of aqueous chlorine and various lipids or tryptophan are nonmutagenic. Nevertheless, additional studies are warranted, so that the toxicological significance of these reaction products can be understood more fully.

  18. The effect of chlorine and combined chlorine/UV treatment on coliphages in drinking water disinfection.

    Science.gov (United States)

    Zyara, Alyaa M; Torvinen, Eila; Veijalainen, Anna-Maria; Heinonen-Tanski, Helvi

    2016-08-01

    Chlorine disinfection is a globally used method to ensure the safety of drinking water. However, it has not always been successful against viruses and, therefore, it is important to find new methods to disinfect water. Seventeen different coliphages were isolated from the treated municipal wastewater. These coliphages and MS2 were treated with different dosages of chlorine in drinking water, and a combined chlorine/ultraviolet irradiation treatment for the chlorine-resistant coliphages. Chlorine disinfection with 0.3-0.5 mg/L total chlorine (free Cl-dosage 0.12-0.21 mg/L) for 10 min achieved 2.5-5.7 Log10-reductions for 11 sensitive coliphages. The six most resistant coliphages showed no reduction with these chlorine concentrations. MS2 was intermediate in chlorine resistance, and thus it is not a good indicator for viruses in chlorine disinfection. In the combined treatment total chlorine of 0.05-0.25 mg/L (free Cl-dosage 0.02-0.08 mg/L) and ultraviolet irradiation (14-22 mWs/cm(2)) were more effective than chlorine alone, and 3-5 Log10-reductions were achieved for the chlorine-resistant strains. The chlorination efficiency could be increased by higher dosages and longer contact times, but this could increase the formation of disinfection by-products. Therefore, the combination treatment is a recommended disinfection method.

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

    NARCIS (Netherlands)

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

    2008-01-01

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

  20. 40 CFR 415.510 - Applicability; description of the potassium iodide production subcategory.

    Science.gov (United States)

    2010-07-01

    ... potassium iodide production subcategory. 415.510 Section 415.510 Protection of Environment ENVIRONMENTAL... SOURCE CATEGORY Potassium Iodide Production Subcategory § 415.510 Applicability; description of the potassium iodide production subcategory. The provisions of this subpart are applicable to...

  1. Potassium chloride production by microcline chlorination

    Energy Technology Data Exchange (ETDEWEB)

    Orosco, Pablo, E-mail: porosco@unsl.edu.ar [Instituto de Investigaciones en Tecnología Química (INTEQUI), Chacabuco y Pedernera, San Luis (Argentina); Facultad de Química, Bioquímica y Farmacia, Universidad Nacional de San Luis, Chacabuco y Pedernera, San Luis (Argentina); Ruiz, María del Carmen [Instituto de Investigaciones en Tecnología Química (INTEQUI), Chacabuco y Pedernera, San Luis (Argentina)

    2015-08-10

    Highlights: • Use of chlorination for the KCl production. • The reagents used were microcline, hydromagnesite and chlorine. • Isothermal and non-isothermal assays were performed in Cl{sub 2}–N{sub 2} mixture. • The chlorination generated KCl at 700 °C. • The chlorination products promote KCl formation. - Abstract: The potassium chloride is one of the most important fertilizers used in agriculture. The current demand of this salt makes interesting the study of potassium chloride production from unconventional potassium resources. In this work the potassium chloride production by chlorination of microcline was investigated. The starting reagents were microcline, hydromagnesite and chlorine. Non-isothermal and isothermal chlorination assays were carried out in a thermogravimetric device adapted to work in corrosive atmospheres. The temperature effect on potassium extraction and the phase transformations produced during chlorination of microcline were studied. The reagents and reaction products were analyzed by X-ray fluorescence (XRF) and X-ray diffraction (XRD). The experimental results indicated that by chlorination of microcline an important extraction of potassium in the temperature range from 800 to 900 °C was produced. Moreover, at 800 °C the forsterite, enstatite and magnesium aluminate spinel phases were generated.

  2. The chlorination of cyclopentanone and cyclohexanone

    NARCIS (Netherlands)

    Maatman, Hendrik

    1980-01-01

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

  3. High resolution spectrophotometry for identification of chlorine dioxide in concentrated chlorine solutions.

    Science.gov (United States)

    Gauw, R D; Emmert, G L; Bubnis, B; Gordon, G

    1999-12-06

    Electrolyzed salt brine generators hold great promise for water disinfection in small communities and remote locations. Electrolysis cell liquors have been reported to contain chlorine, chlorine dioxide and ozone. High resolution spectrophotometry was used to observe the presence (or absence) of a unique spectral absorbance pattern present in solutions containing 1-2 mg/l chlorine dioxide.

  4. The electrosorption of tetraalkylammonium ions on silver iodide

    NARCIS (Netherlands)

    Keizer, de A.

    1981-01-01

    The object of the present investigations was to study the ef fect of the adsorption of charged organic ions on electrically charged, solid-liquid interfaces. To that end, symmetrical quater nary ammonium ions were adsorbed on a silver iodide-electrolyte interface at various surface charges. The elec

  5. Confinement Effects in Low-Dimensional Lead Iodide Perovskite Hybrids

    NARCIS (Netherlands)

    Kamminga, Machteld E.; Fang, Honghua; Filip, Marina R.; Giustino, Feliciano; Baas, Jacobus; Blake, Graeme R.; Loi, Maria Antonietta; Palstra, Thomas T. M.

    2016-01-01

    We use a layered solution crystal growth technique to synthesize high-quality single crystals of phenylalkylammonium lead iodide organic/inorganic hybrid compounds. Single-crystal X-ray diffraction reveals low-dimensional structures consisting of inorganic sheets separated by bilayers of the organic

  6. Radiation-hard polycrystalline mercuric iodide semiconductor particle counters

    Energy Technology Data Exchange (ETDEWEB)

    Schieber, M. [Hebrew Univ., Jerusalem (Israel)]|[Sandia National Laboratories, Livermore Ca 94556 (United States); Zuck, A.; Melekhov, L.; Nissenbaum, J. [Hebrew Univ., Jerusalem (Israel); Turchetta, R.; Dulinski, W.; Husson, D.; Riester, J.L. [LEPSI (ULP/IN2P3), Strasbourg (France)

    1998-06-01

    Mercuric iodide polycrystalline radiation detectors, which can act as nuclear particle counters and for large area imaging devices, have been fabricated using three different methods. Response to X- and gamma rays, beta particles and to 100GeV muons, as well as radiation hardness results are briefly described. (orig.) 8 refs.

  7. 21 CFR 520.763b - Dithiazanine iodide powder.

    Science.gov (United States)

    2010-04-01

    ....763b Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED... is administered to dogs by mixing the proper dosage in the dog's food, using the following dosage... contraindicated in animals sensitive to dithiazanine iodide and should be used cautiously, if at all, in dogs...

  8. FY-2015 Methyl Iodide Deep-Bed Adsorption Test Report

    Energy Technology Data Exchange (ETDEWEB)

    Soelberg, Nicholas Ray [Idaho National Lab. (INL), Idaho Falls, ID (United States); Watson, Tony Leroy [Idaho National Lab. (INL), Idaho Falls, ID (United States)

    2015-09-30

    Nuclear fission produces fission and activation products, including iodine-129, which could evolve into used fuel reprocessing facility off-gas systems, and could require off-gas control to limit air emissions to levels within acceptable emission limits. Deep-bed methyl iodide adsorption testing has continued in Fiscal Year 2015 according to a multi-laboratory methyl iodide adsorption test plan. Updates to the deep-bed test system have also been performed to enable the inclusion of evaporated HNO3 and increased NO2 concentrations in future tests. This report summarizes the result of those activities. Test results showed that iodine adsorption from gaseous methyl iodide using reduced silver zeolite (AgZ) resulted in initial iodine decontamination factors (DFs, ratios of uncontrolled and controlled total iodine levels) under 1,000 for the conditions of the long-duration test performed this year (45 ppm CH3I, 1,000 ppm each NO and NO2, very low H2O levels [3 ppm] in balance air). The mass transfer zone depth exceeded the cumulative 5-inch depth of 4 bed segments, which is deeper than the 2-4 inch depth estimated for the mass transfer zone for adsorbing I2 using AgZ in prior deep-bed tests. The maximum iodine adsorption capacity for the AgZ under the conditions of this test was 6.2% (6.2 g adsorbed I per 100 g sorbent). The maximum Ag utilization was 51%. Additional deep-bed testing and analyses are recommended to (a) expand the data base for methyl iodide adsorption and (b) provide more data for evaluating organic iodide reactions and reaction byproducts for different potential adsorption conditions.

  9. Inactivation of simian rotavirus SA11 by chlorine, chlorine dioxide, and monochloramine.

    OpenAIRE

    Berman, D; Hoff, J C

    1984-01-01

    The kinetics of inactivation of simian rotavirus SA11 by chlorine, chlorine dioxide, and monochloramine were studied at 5 degrees C with a purified preparation of single virions and a preparation of cell-associated virions. Inactivation of the virus preparations with chlorine and chlorine dioxide was studied at pH 6 and 10. The monochloramine studies were done at pH 8. With 0.5 mg of chlorine per liter at pH 6, more than 4 logs (99.99%) of the single virions were inactivated in less than 15 s...

  10. The photoreactivity of chlorine dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Vaida, V. [Univ. of Colorado, Boulder, CO (United States); Simon, J.D. [Univ. of California, San Diego, La Jolla, CA (United States)

    1995-06-09

    Determining the detailed photoreactivity of radicals that are of importance in atmospheric processes requires information from both laboratory and field measurements and theoretical calculations. Laboratory experiments and quantum calculations have been used to develop a comprehensive understanding of the photoreactivity of chlorine dioxide (OClO). The photoreactivity is strongly dependent on the medium (gas phase, liquid solution, or cryogenic matrix). These data reveal details of the complex chemistry of OClO. The potential role of this radical in stratospheric ozone depletion is discussed in accord with these laboratory measurements. 53 refs., 4 figs.

  11. Effects of ozone, chlorine dioxide, chlorine, and monochloramine on Cryptosporidium parvum oocyst viability

    Energy Technology Data Exchange (ETDEWEB)

    Korich, D.G.; Mead, J.R.; Madore, M.S.; Sinclair, N.A.; Sterling, C.R. (Univ. of Arizona, Tucson (USA))

    1990-05-01

    Purified Cryptosporidium parvum oocysts were exposed to ozone, chlorine dioxide, chlorine, and monochloramine. Excystation and mouse infectivity were comparatively evaluated to assess oocyst viability. Ozone and chlorine dioxide more effectively inactivated oocysts than chlorine and monochloramine did. Greater than 90% inactivation as measured by infectivity was achieved by treating oocysts with 1 ppm of ozone (1 mg/liter) for 5 min. Exposure to 1.3 ppm of chlorine dioxide yielded 90% inactivation after 1 h, while 80 ppm of chlorine and 80 ppm of monochloramine required approximately 90 min for 90% inactivation. The data indicate that C. parvum oocysts are 30 times more resistant to ozone and 14 times more resistant to chlorine dioxide than Giardia cysts exposed to these disinfectants under the same conditions. With the possible exception of ozone, the use of disinfectants alone should not be expected to inactivate C. parvum oocysts in drinking water.

  12. Effects of ozone, chlorine dioxide, chlorine, and monochloramine on Cryptosporidium parvum oocyst viability.

    Science.gov (United States)

    Korich, D G; Mead, J R; Madore, M S; Sinclair, N A; Sterling, C R

    1990-01-01

    Purified Cryptosporidium parvum oocysts were exposed to ozone, chlorine dioxide, chlorine, and monochloramine. Excystation and mouse infectivity were comparatively evaluated to assess oocyst viability. Ozone and chlorine dioxide more effectively inactivated oocysts than chlorine and monochloramine did. Greater than 90% inactivation as measured by infectivity was achieved by treating oocysts with 1 ppm of ozone (1 mg/liter) for 5 min. Exposure to 1.3 ppm of chlorine dioxide yielded 90% inactivation after 1 h, while 80 ppm of chlorine and 80 ppm of monochloramine required approximately 90 min for 90% inactivation. The data indicate that C. parvum oocysts are 30 times more resistant to ozone and 14 times more resistant to chlorine dioxide than Giardia cysts exposed to these disinfectants under the same conditions. With the possible exception of ozone, the use of disinfectants alone should not be expected to inactivate C. parvum oocysts in drinking water. PMID:2339894

  13. Mutagenic compounds from chlorination of humic substances

    Science.gov (United States)

    Holmbom, Bjarne

    Chlorination of natural humic substances, as well as of lignin, produces a myriad of non-chlorinated and chlorinated compounds. The identification of an important class of strongly mutagenic compounds is reviewed. The most important Ames mutagen in chlorinated drinking waters of various origin is the compound 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone ("MX"). This compound occurs at neutral pH in the acyclic form, i.e. in the form of Z-2-chloro-3-(dichloromethyl)-4-oxobutenoic acid. Its E-isomer (E-MX) is present in chlorinated drinking waters at a similar concentration, but is less mutagenic in Ames test. Both oxidised and reduced forms of MX and E-MX are also present in chlorinated waters. The present knowledge of the chemistry and toxicology of these mutagens is examined. The formation and possible elimination of the chlorination mutagens is discussed. The need of understanding the mechanisms of formation of these mutagens from humic substances during drinking water chlorination is emphasized.

  14. Elements from chlorine to calcium nuclear reactions

    CERN Document Server

    Kunz, Wunibald

    1968-01-01

    Nuclear Tables: Part II Nuclear Reactions, Volume 3: The Elements from Chlorine to Calcium contains tabulations of the nuclear reaction values of elements chlorine, argon, potassium, and calcium. These tabulations provide the calculated Q-values of the elements and their isotopes. This book will be of value to general chemistry researchers.

  15. Internal chlorination of Ni-Cr alloys

    Energy Technology Data Exchange (ETDEWEB)

    Berztiss, D.; Hennesen, K.; Grabke, H.J. [Max-Planck-Institut fuer Eisenforschung GmbH, Duesseldorf (Germany)

    1998-12-31

    In contrast to internal oxidation, sulfidation and carburization, very little information is available regarding internal chlorination, especially diffusion of chlorine in metallic alloys. This paper describes results of experiments on Ni-Cr alloys (<10 wt% Cr) exposed in an atmosphere containing radioactive HCl. The diffusion of chlorine in the alloy can be determined by measurement of residual {beta}-activity from the sample surface. Successively thin layers (0.5-10 {mu}m) of the alloy were removed by lapping and the surface activity was measured to obtain a depth profile. Both single and polycrystalline materials were tested. Through this work it should be determined if there is in fact solubility and diffusion of chlorine in Ni-based alloys as some authors have proposed or if the ingress of chlorine is mainly a grain boundary phenomenon. (orig.)

  16. Defective organification of iodide causing congenital goitrous hypothyroidism.

    Science.gov (United States)

    Ishikawa, N; Eguchi, K; Ohmori, T; Momotani, N; Nagayama, Y; Hosoya, T; Oguchi, H; Mimura, T; Kimura, S; Nagataki, S; Ito, K

    1996-01-01

    A 26-yr-old Japanese woman with congenital goitrous hypo-thyroidism and sensorineural deafness underwent a thyroidectomy. Examination of the thyroid gland revealed characteristic features of multinodular goiter. The T3 and T4 content in thyroglobulin (Tg) were 0.03 and 0.02 mol/mol Tg, respectively. Iodide incorporation into Tg, using slices of the thyroid tissue, revealed that iodide organification of thyroid tissue from our patient was markedly lower than that of normal controls. Then, guaiacol and iodide oxidation activities of thyroid peroxidase (TPO) in our patient's thyroid tissue were lower than those of normal controls (guaiacol assay: 1.92 vs. 30.0 +/- 5.7 mGU/mg protein; iodide assay: 1.1 vs. 6.6 +/- 2.8 mIU/mg protein). Lineweaver-Burk plot analysis of the oxidation rates of guaiacol and iodide indicated that this patient's TPO had a defect in the binding of guaiacol and iodide, but the coupling activity of the patient's TPO was not decreased compared with those of two normal thyroids. In this case and in control subjects, Nothern gel analysis of TPO messenger RNA from unstimulated and TSH-stimulated thyroid cells revealed a 3.2 kilobase species in the former and four distinct messenger RNA species of 4.0, 3.2, 2.1, and 1.7 kilobases in the latter. Western blot analysis of TPOs obtained from this patient and from control subjects identified the same 107 kDa protein, using antimicrosomal antibody-positive serum. We analyzed the coding sequence in the patient's TPO gene by using polymerase chain reaction technique. A single point mutation of G-->C at 1265 base pair was detected only in the TPO gene, but this point mutation does not alter the amino acid residue. It is possible that posttranslational modification such as abnormal glycosylation may occur in the TPO molecules. Furthermore, it is possible that there are differences in the tertiary structures of the TPO molecules between our patient and normal subjects. The above abnormalities of TPO molecules

  17. [Evaluation of potassium iodide in Polish dietary salt].

    Science.gov (United States)

    Andrzejewska, E; Rokicka, B; Gajda, J; Jarecka, J; Oraczewska, A; Karłowski, K

    1996-01-01

    The consequences of iodine deficiency occurring still in Poland include serious health disorders in the population, such as psycho- somatic retardation, hypothyroidism, endemic goitre, even cretinism. Administration of iodized edible salt with daily diet is an effective method for prevention of iodine deficiency. The condition of success is the proper level of potassium iodide in this salt and adequate distribution of iodized salt in various regions of the country. Successful iodine prophylaxis should be based on iodination of edible salt in amounts of 30 +/- 10 mg of KJ/kg. The permission given in the period from February to May 1994 by the General Sanitary Inspector for the production and marketing of edible salt iodized in proportions of 30 +/- 10 mg KJ/kg opened the possibility of starting its production in salt mines. The purpose of the presently reported work was to assess, in cooperation with the Province Sanitary Epidemiological Stations, the adequacy of iodination of the Polish edible salt produced in the years 1994-1995. The study was carried out according to the Polish Standard "Salt (Sodium Chloride) /PN-80/C-84081.35. Potassium iodide determination by photo colorimetric method." In 1995 the number of edible salt samples analyzed was 2484, and this number included 2129 samples of iodized salt. Potassium iodide content agreeing with the above permission was found in 122 samples, that is in 57.4% of iodized salt samples. In 603 samples (28.3%) of iodized salt this content was below that given in the permissions. In 1994 this study was carried out taking 2172 samples of edible salt, including 1586 samples of iodized salt. The content of potassium iodide agreeing with the permissions (30 +/- 10 mg/kg) was found in 342 samples (28, 1%), but 272 (22.4%) samples of iodized salt produced by salt mines contained lower amounts of potassium iodide than the amount indicated in the permissions, but still within the limits set down in the Polish Standard (20 +/- 5 mg

  18. Purification and deposition of silicon by an iodide disproportionation reaction

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Tihu (Littleton, CO); Ciszek, Theodore F. (Evergreen, CO)

    2002-01-01

    Method and apparatus for producing purified bulk silicon from highly impure metallurgical-grade silicon source material at atmospheric pressure. Method involves: (1) initially reacting iodine and metallurgical-grade silicon to create silicon tetraiodide and impurity iodide byproducts in a cold-wall reactor chamber; (2) isolating silicon tetraiodide from the impurity iodide byproducts and purifying it by distillation in a distillation chamber; and (3) transferring the purified silicon tetraiodide back to the cold-wall reactor chamber, reacting it with additional iodine and metallurgical-grade silicon to produce silicon diiodide and depositing the silicon diiodide onto a substrate within the cold-wall reactor chamber. The two chambers are at atmospheric pressure and the system is open to allow the introduction of additional source material and to remove and replace finished substrates.

  19. Synthesis and Structure of Bis(4-nitrobenzaldehyde thiosemicarbazone) Cadmium Iodide

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The title complex, bis(4-nitrobenzaldehyde thiosemicarbazone) cadmium iodide (C16H16CdI2N8O4S2) crystallizes in the triclinic system, space group P1 with a=9.632(2), b=11.227(2), c=14.031(3), α= 67.50(3), β= 86.99(3), γ= 66.64(3)°, V=1278.13, Z = 2, Dc = 2.117gcm-3, F(000) = 772, μ =3.472mm-1 MoKα radiation (λ=0.71073), R = 0.0443, wR= 0.1425 for 4529 observed reflections [I>2σ(I)] of 4731 independent reflections. The result shows that the structure contains CdL2I2 (where L = 4-nitrobenzaldehyde thiosemicarbazone) distorted tetrahedral units in which the two ligands are S-bonded as monodentate to cadmium ion; the two iodide ions are also coordinated to Cd(II).

  20. Caloric Effects in Methylammonium Lead Iodide from Molecular Dynamics Simulations

    OpenAIRE

    Liu, Shi; Cohen, Ronald E.

    2016-01-01

    Organic-inorganic hybrid perovskite architecture could serve as a robust platform for materials design to realize functionalities beyond photovoltaic applications. We explore caloric effects in organometal halide perovskites, taking methylammonium lead iodide (MAPbI$_3$) as an example, using all-atom molecular dynamics simulations with a first-principles based interatomic potential. The adiabatic thermal change is estimated directly by introducing different driving fields in the simulations. ...

  1. Structural insight into iodide uptake by AFm phases.

    Science.gov (United States)

    Aimoz, Laure; Wieland, Erich; Taviot-Guého, Christine; Dähn, Rainer; Vespa, Marika; Churakov, Sergey V

    2012-04-03

    The ability of cement phases carrying positively charged surfaces to retard the mobility of (129)I, present as iodide (I(-)) in groundwater, was investigated in the context of safe disposal of radioactive waste. (125)I sorption experiments on ettringite, hydrotalcite, chloride-, carbonate- and sulfate-containing AFm phases indicated that calcium-monosulfate (AFm-SO(4)) is the only phase that takes up trace levels of iodide. The structures of AFm phases prepared by coprecipitating iodide with other anions were investigated in order to understand this preferential uptake mechanism. X-ray diffraction (XRD) investigations showed a segregation of monoiodide (AFm-I(2)) and Friedel's salt (AFm-Cl(2)) for I-Cl mixtures, whereas interstratifications of AFm-I(2) and hemicarboaluminate (AFm-OH-(CO(3))(0.5)) were observed for the I-CO(3) systems. In contrast, XRD measurements indicated the formation of a solid solution between AFm-I(2) and AFm-SO(4) for the I-SO(4) mixtures. Extended X-ray absorption fine structure spectroscopy showed a modification of the coordination environment of iodine in I-CO(3) and in I-SO(4) samples compared to pure AFm-I(2). This is assumed to be due to the introduction of stacking faults in I-CO(3) samples on one hand and due to the presence of sulfate and associated space-filling water molecules as close neighbors in I-SO(4) samples on the other hand. The formation of a solid solution between AFm-I(2) and AFm-SO(4), with a short-range mixing of iodide and sulfate, implies that AFm-SO(4) bears the potential to retard (129)I.

  2. Development of the strontium iodide coded aperture (SICA) instrument

    Science.gov (United States)

    Mitchell, Lee J.; Phlips, Bernard F.; Grove, J. Eric; Cordes, Ryan

    2015-08-01

    The work reports on the development of a Strontium Iodide Coded Aperture (SICA) instrument for use in space-based astrophysics, solar physics, and high-energy atmospheric physics. The Naval Research Laboratory is developing a prototype coded aperture imager that will consist of an 8 x 8 array of SrI2:Eu detectors, each read out by a silicon photomultiplier. The array would be used to demonstrate SrI2:Eu detector performance for space-based missions. Europium-doped strontium iodide (SrI2:Eu) detectors have recently become available, and the material is a strong candidate to replace existing detector technology currently used for space-based gamma-ray astrophysics research. The detectors have a typical energy resolution of 3.2% at 662 keV, a significant improvement over the 6.5% energy resolution of thallium-doped sodium iodide. With a density of 4.59 g/cm and a Zeff of 49, SrI2:Eu has a high efficiency for MeV gamma-ray detection. Coupling this with recent improvements in silicon photomultiplier technology (i.e., no bulky photomultiplier tubes) creates high-density, large-area, low-power detector arrays with good energy resolution. Also, the energy resolution of SrI2:Eu makes it ideal for use as the back plane of a Compton telescope.

  3. Gold nanoelectrode ensembles for direct trace electroanalysis of iodide.

    Science.gov (United States)

    Pereira, Francisco C; Moretto, Ligia M; De Leo, Manuela; Zanoni, Maria V Boldrin; Ugo, Paolo

    2006-08-01

    A procedure for the standardization of ensembles of gold nanodisk electrodes (NEE) of 30 nm diameter is presented, which is based on the analytical comparison between experimental cyclic voltammograms (CV) obtained at the NEEs in diluted solutions of redox probes and CV patterns obtained by digital simulation. Possible origins of defects sometimes found in NEEs are discussed. Selected NEEs are then employed for the study of the electrochemical oxidation of iodide in acidic solutions. CV patterns display typical quasi-reversible behavior which involves associated chemical reactions between adsorbed and solution species. The main CV characteristics at the NEE compare with those observed at millimeter sized gold disk electrodes (Au-macro), apart a slight shift in E1/2 values and slightly higher peak to peak separation at the NEE. The detection limit (DL) at NEEs is 0.3 microM, which is more than one order of magnitude lower than DL at the Au-macro (4 microM). The mechanism of the electrochemical oxidation of iodide at NEEs is discussed. Finally, NEEs are applied to the direct determination of iodide at micromolar concentration levels in real samples, namely in some ophthalmic drugs and iodized table salt.

  4. Enhanced iodide sequestration by 3-biphenyl-5,6-dihydroimidazo 2,1-b thiazole in sodium/iodide sym-porter (NIS)-expressing cells

    Energy Technology Data Exchange (ETDEWEB)

    Lecat-Guillet, N.; Ambroise, Y. [CEA, DSV, Dept Bioorgan Chem andt IsotopLabelling, Inst Biol and Technol, iBiTecS, F-91191 Gif Sur Yvette (France)

    2008-07-01

    The ability of the sodium/iodide sym-porter (NIS) to take up iodide has long provided the basis for cyto-reductive gene therapy and cancer treatment with radio-iodide. One of the major limitations of this approach is that radio-iodide retention in NIS-expressing cells is not sufficient for their destruction. We identified and characterized a small organic molecule capable of increasing iodide retention in HEK293 cells permanently transfected with human NIS cDNA (hNIS-HEK293) and in the rat thyroid-derived cell line FRTL-5. In the presence of 3-biphenyl-4'-yl-5,6-dihydroimidazo[2,1-b)thiazole (ISA1), the transmembrane iodide concentration gradient was increased up to 4.5-fold. Our experiments indicate that the imidazo-thiazole derivative acts either by inhibiting anion efflux mechanisms, or by promoting the relocation of iodide into subcellular compartments. This new compound is not only an attractive chemical tool to investigate the mechanisms of iodide flux at the cellular level, but also opens promising perspectives in the treatment of cancer after NIS gene transfer. (authors)

  5. Removal and sequestration of iodide using silver-impregnated activated carbon.

    Science.gov (United States)

    Hoskins, Jay S; Karanfil, Tanju; Serkiz, Steven M

    2002-02-15

    Two silver-impregnated activated carbons (SIACs) (0.05 and 1.05 wt % silver) and their virgin (i.e., unimpregnated) granular activated carbon (GAC) precursors were investigated for their ability to remove and sequester iodide from aqueous solutions in a series of batch sorption and leaching experiments. Silver content, total iodide concentration, and pH were the factors controlling the removal mechanisms of iodide. Iodide uptake increased with decreasing pH for both SIACs and their virgin GACs. The 0.05% SIAC behaved similarly to its virgin GAC in all experimental conditions because of its low silver content. At pH values of 7 and 8 there was a marked increased in iodide removal for the 1.05% SIAC over that of its virgin GAC, while their performances were similar at a pH of 5. Scanning electron microscopy (SEM) and energy-dispersive X-ray (EDX) analyses prior to reaction with iodide showed the presence of metallic silver agglomerates on the 1.05% SIAC surface. After the reaction, elemental mapping with EDX showed the formation of silver iodide agglomerates. Oxidation of metallic silver was observed in the presence of oxygen, and the carbon surface appears to catalyze this reaction. When the molar ratio of silver to iodide was greater than 1 (i.e., M(Ag,SIAC) > M(I,TOTAL)), precipitation of silver iodide was the dominant removal mechanism. However, unreacted silver leached into solution with decreasing pH while iodide leaching did not occur. When M(Ag,SIAC) silver iodide precipitation occurred until all available silver had reacted, and additional iodide was removed from solution by pH-dependent adsorption to the GAC. Under this condition, silver leaching did not occur while iodide leaching increased with increasing pH.

  6. Chlorination of Wastewater, Manual of Practice No. 4.

    Science.gov (United States)

    Water Pollution Control Federation, Washington, DC.

    This manual reviews chlorination practices in the treatment and disposal of wastes from the earliest known applications. The application of chlorination for various purposes is described but no attempt has been made to compare chlorination with other methods. Included are chapters on the development and practice of wastewater chlorination,…

  7. Electron affinity of chlorine dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Babcock, L.M.; Pentecost, T.; Koppenol, W.H. (Louisiana State Univ., Baton Rouge (USA))

    1989-12-14

    The flowing afterglow technique was used to determine the electron affinity of chlorine dioxide. A value of 2.37 {plus minus} 0.10 eV was found by bracketing between the electron affinities of HS* and SF{sub 4} as a lower limit and that of NO{sub 2} as an upper limit. This value is in excellent agreement with 2.32 eV predicted from a simple thermodynamic cycle involving the reduction potential of the ClO{sub 2}/ClO{sub 2}{sup {minus}} couple and a Gibbs hydration energy identical with that of SO{sub 2}{sup {sm bullet}{minus}}.

  8. Electrochemistry of silver iodide the capacity of the double layer at the silver iodide-water interface

    NARCIS (Netherlands)

    Lyklema, J.; Overbeek, J.Th.G.

    1961-01-01

    A method is described for obtaining differential double layer capacities on silver iodide. Especially the influence of the nature and concentration of indifferent electrolytes was investigated, viz., the nitrates of Li·, K·, Rb·, NH4·, H·, Tl·, Mg··, Ba··, Co··, Cd··, Pb··, La···, Th····, the fluori

  9. Phosphate valorization by dry chlorination route

    OpenAIRE

    Kanari N.; Menad N.; Diot F.; Allain E.; Yvon J.

    2016-01-01

    International audience; This work deals with the extraction of phosphorus chlorinated compounds from phosphate materials using chlorination with gaseous chlorine. An industrial sample of dicalcium phosphate dihydrate, after transformation into calcium pyrophosphate (Ca 2 P 2 O 7), is subjected to reactions with Cl 2 +CO+N 2 and Cl 2 +C+N 2 at temperatures ranging from 625 to 950 °C using boat experiments. Gathering results of the thermodynamic predictions and TG/DT analysis with those of SEM ...

  10. A comparison of the virucidal properties of chlorine, chlorine dioxide, bromine chloride and iodine.

    OpenAIRE

    Taylor, G. R.; Butler, M.

    1982-01-01

    Chlorine dioxide, bromine chloride and iodine were compared with chlorine as virucidal agents. Under optimal conditions all disinfectants were effective at low concentrations, but each disinfectant responded differently to acidity and alkalinity. Disinfection by chlorine was impaired by the presence of ammonia, but the other disinfectants retained much of their potency. Disinfection of poliovirus by iodine resulted in structural changes in the virions as seen by electron micrroscopy, but the ...

  11. Behavior of chlorine during coal pyrolysis

    Science.gov (United States)

    Shao, D.; Hutchinson, E.J.; Cao, H.; Pan, W.-P.; Chou, C.-L.

    1994-01-01

    The behavior of chlorine in Illinois coals during pyrolysis was evaluated by combined thermo-gravimetry-Fourier transform infrared spectroscopy-ion chromatography (TG-FTIR-IC) techniques. It was found that more than 90% of chlorine in Illinois coals (IBC-103, 105, 106, and 109) was liberated as HCl gas during pyrolysis from 300 to 600??C, with the rate reaching a maximum at 440 ??C. Similarity of the HCl and NH3 release profiles during pyrolysis of IBC-109 supports the hypothesis that the chlorine in coal may be associated with nitrogen and the chlorine is probably bonded to the basic nitrogen sites on the inner walls of coal micropores. ?? 1994 American Chemical Society.

  12. Chlorine Salts at the Phoenix Landing Site

    Science.gov (United States)

    Hanley, J.; Horgan, B.

    2016-09-01

    Although chlorine salts (perchlorates, chlorides) are known to exist at the Phoenix landing site, their distribution and type have not been positively identified yet. We look for these salts through a novel NIR remote sensing technique.

  13. Iron- Catalyzed 1,2-Addition of Perfluoroalkyl Iodides to Alkynes and Alkenes

    OpenAIRE

    Xu, Tao; Cheung, Chi Wai; Hu, Xile

    2014-01-01

    Iron catalysis has been developed for the intermolecular 1,2-addition of perfluoroalkyl iodides to alkynes and alkenes. The catalysis has a wide substrate scope and high functional-group tolerance. A variety of perfluoroalkyl iodides including CF3I can be employed. The resulting perfluoroalkylated alkyl and alkenyl iodides can be further functionalized by cross-coupling reactions. This methodology provides a straightforward and streamlined access to perfluoroalkylated organic molecules.

  14. Hydrochloric acid recycling from chlorinated hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Sowieja, D. [Sulzer Escher Wyss GmbH, Ravensburg (Germany); Schaub, M. [Sulzer Chemtech Ltd., Winterthur (Switzerland)

    1993-12-31

    Chlorinated hydrocarbons present a major ecological hazard since most of them are only poorly biodegradable. Incineration is an economical process for their destruction, however the usually recovered sodium or calcium chlorides do not present a value and their disposal may even be very costly. Recovery of hydrochloric acid may therefore present an economical solution, mainly were large quantities of highly chlorinated compounds can be processed (author) 6 refs., 4 figs., 1 tab.

  15. Modeling Trihalomethane Formation Potential from Wastewater Chlorination

    Science.gov (United States)

    1994-09-01

    chemically with each other, and with living organisms, particularly bacteria ( Manahan , 1991:435). To ensure effective disinfection, to meet the CWA...halogens are strong oxidants and are highly reactive ( Manahan , 1991:504). Chlorine is never found uncombined in nature, it exists only as the...HOCI) according to the following reaction: Cl2 (gas) + H20 =• HOC1 + H+ + Cl The hydrogen is oxidized and the chlorine gas is reduced ( Manahan , 1991

  16. Chlorinated drinking water for lightweight laying hens

    Directory of Open Access Journals (Sweden)

    A.F. Schneider

    Full Text Available ABSTRACT The study aimed to evaluate the effect of different levels of chlorine in drinking water of laying hens on zootechnical performance, eggs shell quality, hemogasometry levels and calcium content in tibia. 144 Hy-Line laying hens, 61 weeks old, were used distributed in 24 metabolism cages. They were subjected to water diets, for a period of 28 days, using sodium hypochlorite as a chlorine source in order to obtain the following concentrations: 5ppm (control, 20ppm, 50ppm, and 100ppm. Their performance was evaluated through water consumption, feed intake, egg production and weight, egg mass, feed conversion. Shell quality was measured by specific gravity. At the end of the experiment, arterial blood was collected for blood gas level assessment and a poultry of each replicate was sacrificed to obtain tibia and calcium content measurement. There was a water consumption reduction from 20ppm of chlorine and feed intake reduction in poultry receiving water with 100ppm of chlorine. The regression analysis showed that the higher the level of chlorine in water, the higher the reduction in consumption. There were no differences in egg production and weight, egg mass, feed conversion, specific gravity, tibia calcium content, and hemogasometry levels (hydrogenionic potential, carbon dioxide partial pressure, oxygen partial pressure, sodium, potassium, chloride, bicarbonate, carbon dioxide total concentration, anion gap and oxygen saturation. The use of levels above 5ppm of chlorine is not recommended in the water of lightweight laying hens.

  17. Expression of sodium-iodide symporter in thyroid gland tumors: immunohistochemical study

    Directory of Open Access Journals (Sweden)

    Bondarenko O.O.

    2009-01-01

    Full Text Available One of the key moments of radioiodine therapy, and also radioisotope diagnostics of cancers of a thyroid gland is ability of their cells to accumulate iodide. This ability is provided with activity of the specific transporter – sodium-iodide symporter. Our research has shown disorders of sodium-iodide symporter immunoexpression in all tumors of thyroid gland: from overexpression and absence of plasma membrane expression in differentiated carcinomas, up to weak or actually absent in low differentiated cancers and Hurtle-cells tumors. Thus, there is a prospect of application of the sodium-iodide symporter, as the prognostic marker of thyroid cancers.

  18. Optical properties and surface morphology studies of palladium contacts on mercuric iodide single crystals

    Energy Technology Data Exchange (ETDEWEB)

    George, M.A.; Azoulay, M.; Burger, A.; Biao, Y.; Silberman, E. [Fisk Univ., Nashville, TN (United States). Dept. of Physics; Nason, D. [EG and G Energy Measurements, Inc., Goleta, CA (United States). Santa Barbara Operations

    1993-05-01

    Palladium is chemically suitable for electric contacts on mercuric iodide detectors for photon and nuclear radiation detection, so the understanding of palladium contacts is important for fundamental and practical scientific purposes. A study has been conducted on the surface morphology of evaporated contacts using Atomic Force Microscopy (AFM) and optical transmission and reflection. Evaporated palladium coatings are typically nonuniform and may deposit selectively on mercuric iodide surface defects. Reflection measurements show that coating thickness and surface treatment affect intensity, position and shape of a reflected peak characteristic of the mercuric iodide structure. Results indicate that the band gap energy in the surface of the mercuric iodide is lowered by palladium contacts.

  19. Optical properties and surface morphology studies of palladium contacts on mercuric iodide single crystals

    Science.gov (United States)

    George, M. A.; Azoulay, M.; Burger, A.; Biao, Y.; Silberman, E.; Nason, D.

    1993-04-01

    Palladium is chemically suitable for electric contacts on mercuric iodide detectors for photon and nuclear radiation detection, so the understanding of palladium contacts is important for fundamental and practical scientific purposes. A study has been conducted on the surface morphology of evaporated contacts using atomic force microscopy (AFM) and optical transmission and reflection. Evaporated palladium coatings are typically nonuniform and may deposit selectively on mercuric iodide surface defects. Reflection measurements show that coating thickness and surface treatment affect intensity, position, and shape of a reflected peak characteristic of the mercuric iodide structure. Results indicate that the band gap energy in the surface of the mercuric iodide is lowered by palladium contacts.

  20. Strontium iodide gamma ray spectrometers for planetary science (Conference Presentation)

    Science.gov (United States)

    Prettyman, Thomas H.; Rowe, Emmanuel; Butler, Jarrhett; Groza, Michael; Burger, Arnold; Yamashita, Naoyuki; Lambert, James L.; Stassun, Keivan G.; Beck, Patrick R.; Cherepy, Nerine J.; Payne, Stephen A.; Castillo-Rogez, Julie C.; Feldman, Sabrina M.; Raymond, Carol A.

    2016-09-01

    Gamma rays produced passively by cosmic ray interactions and by the decay of radioelements convey information about the elemental makeup of planetary surfaces and atmospheres. Orbital missions mapped the composition of the Moon, Mars, Mercury, Vesta, and now Ceres. Active neutron interrogation will enable and/or enhance in situ measurements (rovers, landers, and sondes). Elemental measurements support planetary science objectives as well as resource utilization and planetary defense initiatives. Strontium iodide, an ultra-bright scintillator with low nonproportionality, offers significantly better energy resolution than most previously flown scintillators, enabling improved accuracy for identification and quantification of key elements. Lanthanum bromide achieves similar resolution; however, radiolanthanum emissions obscure planetary gamma rays from radioelements K, Th, and U. The response of silicon-based optical sensors optimally overlaps the emission spectrum of strontium iodide, enabling the development of compact, low-power sensors required for space applications, including burgeoning microsatellite programs. While crystals of the size needed for planetary measurements (>100 cm3) are on the way, pulse-shape corrections to account for variations in absorption/re-emission of light are needed to achieve maximum resolution. Additional challenges for implementation of large-volume detectors include optimization of light collection using silicon-based sensors and assessment of radiation damage effects and energetic-particle induced backgrounds. Using laboratory experiments, archived planetary data, and modeling, we evaluate the performance of strontium iodide for future missions to small bodies (asteroids and comets) and surfaces of the Moon and Venus. We report progress on instrument design and preliminary assessment of radiation damage effects in comparison to technology with flight heritage.

  1. Electronic properties and Compton profiles of silver iodide

    Indian Academy of Sciences (India)

    Alpa Dashora; Ambica Marwal; K R Soni; B L Ahuja

    2010-06-01

    We have carried out an extensive study of electronic properties of silver iodide in - and -phases. The theoretical Compton profiles, energy bands, density of states and anisotropies in momentum densities are computed using density functional theories. We have also employed full-potential linearized augmented plane-wave method to derive the energy bands and the density of states. To compare our theoretical data, isotropic Compton profile measurement on -AgI using 137Cs Compton spectrometer at an intermediate resolution of 0.38 a.u. has been undertaken. The theoretical anisotropies are also interpreted on the basis of energy bands.

  2. Temperature dependent energy levels of methylammonium lead iodide perovskite

    Energy Technology Data Exchange (ETDEWEB)

    Foley, Benjamin J.; Marlowe, Daniel L.; Choi, Joshua J., E-mail: jjc6z@virginia.edu, E-mail: mgupta@virginia.edu, E-mail: scudiero@wsu.edu [Department of Chemical Engineering, University of Virginia, Charlottesville, Virginia 22904 (United States); Sun, Keye; Gupta, Mool C., E-mail: jjc6z@virginia.edu, E-mail: mgupta@virginia.edu, E-mail: scudiero@wsu.edu [Department of Electrical and Computer Engineering, University of Virginia, Charlottesville, Virginia 22904 (United States); Saidi, Wissam A. [Department of Mechanical Engineering and Materials Science, University of Pittsburgh, Pittsburgh, Pennsylvania 15261 (United States); Scudiero, Louis, E-mail: jjc6z@virginia.edu, E-mail: mgupta@virginia.edu, E-mail: scudiero@wsu.edu [Chemistry Department and Materials Science and Engineering Program, Washington State University, Pullman, Washington 99164 (United States)

    2015-06-15

    Temperature dependent energy levels of methylammonium lead iodide are investigated using a combination of ultraviolet photoemission spectroscopy and optical spectroscopy. Our results show that the valence band maximum and conduction band minimum shift down in energy by 110 meV and 77 meV as temperature increases from 28 °C to 85 °C. Density functional theory calculations using slab structures show that the decreased orbital splitting due to thermal expansion is a major contribution to the experimentally observed shift in energy levels. Our results have implications for solar cell performance under operating conditions with continued sunlight exposure and increased temperature.

  3. Polarized spectral complexes of optical functions of monovalent mercury iodide

    Science.gov (United States)

    Sobolev, V. V.; Sobolev, V. Val.; Anisimov, D. V.

    2015-12-01

    Spectral complexes of optical functions of monovalent mercury iodide Hg2I2 were determined for E ⊥ c and E || c polarizations in the range from 2 to 5.5 eV at 4.2 K. The permittivity and characteristic electron energy loss spectra were expanded in simple components with the determination of their main parameters, including the energy of the maximum and the oscillator strength. The calculations were performed based on known reflectance spectra. Computer programs based on Kramers-Kronig relations and the improved parameter-free method of Argand diagrams were used.

  4. Electrolytic coloration of hydroxyl-doped potassium iodide polycrystals

    Science.gov (United States)

    Wang, Na; Gu, Hongen; Han, Li; Guo, Meili; Qin, Fang

    2007-03-01

    Hydroxyl-doped potassium iodide polycrystals were successfully colored electrolytically by using a pointed cathode and a flat anode at various temperatures and electric field strengths, which mainly benefits appropriate coloration temperatures and electric field strengths. Characteristic OH-, O2--Va+ , U, V2, V3, Cu+, Cu-related, I2- , I2, K, F, R1 and R2 spectral bands were observed in Kubelka-Munk functions of the colored polycrystals, and the OH- and O2--Va+ spectral bands at room temperature were determined from Mollwo-Ivey plots. Color center formation in the electrolytic coloration was explained.

  5. A new kind of Molotov? Gasoline-pool chlorinator mixtures.

    Science.gov (United States)

    Hutches, Katherine; Lord, James

    2012-07-01

    This paper investigates the reaction between pool chlorinators and gasoline. In particular, the propensity for self-ignition and the resulting chemical products were studied. An organic pool chlorinator was combined with gasoline in varying proportions in an attempt to form a hypergolic mixture. None of the combinations resulted in self-ignition, but larger quantities of chlorinator produced vigorous light-colored smoke and a solid mass containing isocyanuric acid and copper chloride. Additionally, the chlorinating abilities of different commercially available pool chlorinators were explored. When Ca(ClO)(2) and sodium dichloro-s-triazinetrione-based chlorinators were used, the presence of gasoline was still visible after 10 days, despite limited chlorination. The trichloro-s-triazinetrione-based chlorinator, however, caused efficient chlorination of the C(2)- and C(3)-alkylbenzenes, making gasoline no longer identifiable.

  6. Maxillofacial prostheses of chlorinated polyethylene.

    Science.gov (United States)

    May, P D

    1978-05-01

    There is clearly a need for maxillofacial prosthetic materials with improved properties. The chlorinated polyethylenes are thermoplastic elastomers which have particularly promising properties, and were used by us to prepare improved maxillofacial prostheses. Suitable CPE resins were compounded with other polymers and with pigments on a heated rubber mill to form thin sheets in a variety of shades. These were heated at 190 degrees C for 10 min and placed between heated linotype mold halves. The prosthesis was formed in a hand press. Sometimes heating and pressing were repeated. After cooling in water, the prosthesis was removed and hand-shaded with oil-soluble dyes. Physical properties were evaluated using standard techniques; skin irritation studies were conducted by 14-day insult patch tests on rabbits. Clinical evaluations were conducted on human volunteers. Parallel evaluations were conducted on commerically available materials for comparison. The CPE was superior to all of the three commerical materials in most properties, and comparable to the better of the three in the remaining properties. On balance, CPE was significantly superior. Early results indicate that the materials and techniques required are easily handled in the dental lab and that the final prosthesis has excellent aesthetic and patient acceptability.

  7. Chlorine Abundances in Cool Stars

    CERN Document Server

    Maas, Z G; Hinkle, K

    2016-01-01

    Chlorine abundances are reported in 15 evolved giants and one M dwarf in the solar neighborhood. The Cl abundance was measured using the vibration-rotation 1-0 P8 line of H$^{35}$Cl at 3.69851 $\\mu$m. The high resolution L-band spectra were observed using the Phoenix infrared spectrometer on the Kitt Peak Mayall 4m telescope. The average [$^{35}$Cl/Fe] abundance in stars with --0.72$<$[Fe/H]$<$0.20 is [$^{35}$Cl/Fe]=(--0.10$\\pm$0.15) dex. The mean difference between the [$^{35}$Cl/Fe] ratios measured in our stars and chemical evolution model values is (0.16$\\pm$0.15) dex. The [$^{35}$Cl/Ca] ratio has an offset of $\\sim$0.35 dex above model predictions suggesting chemical evolution models are under producing Cl at the high metallicity range. Abundances of C, N, O, Si, and Ca were also measured in our spectral region and are consistent with F and G dwarfs. The Cl versus O abundances from our sample match Cl abundances measured in planetary nebula and \\ion{H}{2} regions. In one star where both H$^{35}$Cl a...

  8. Reactions of polynuclear aromatic hydrocarbons with chlorine and chlorine dioxide in coal tar lined pipes

    Energy Technology Data Exchange (ETDEWEB)

    Merkel, T.; Maier, M.; Sacher, F.; Maier, D. [University of Karlsruhe, Karlsruhe (Germany). Engler Bunte Institut

    1997-12-31

    In the presence of disinfectants, PAH are remobilised from the coal tar lining of water distribution mains. Reactions of the PAH with chlorine and chlorine dioxide can lead to chlorinated PAH that might show higher mutagenic effects that the parent PAH. Detection limits in the lower nanogram-per-litre level for the determination of PAH and chlorinated PAH were achieved by using solid phase micro extraction and a gas chromatographic mass spectrometric device. Thus, the reactions of four PAH (anthracene, fluoranthene, fluorene and phenanthrene) with chlorine and chlorine dioxide under conditions and at concentrations of common practice in the drinking water distribution system could be investigated. In batch experiments with demineralised and drinking water at pH 7, the concentrations of fluoranthene, fluorene and phenanthrene remained constant, whereas anthracene reacted quantitatively with both disinfectants. The reaction of anthracene followed by pseudo-first order kinetics. In these reactions no chlorinated products could be detected, only monohydroxyanthracene and anthraquinone were identified. The toxic effect of a set of chlorinated and oxidised PAH was also examined.

  9. Bromate ion formation in dark chlorination and ultraviolet/chlorination processes for bromide-containing water

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Bormate (BrO3-) is a carcinogenic chemical produced in ozonation or chlorination of bromide-containing water. Although its formation in seawater with or without sunlight has been previously investigated, the formation of bromate in dilute solutions,particularly raw water for water treatment plant, is unknown. In this article, the results of bench scale tests to measure the formation rates of bromate formation in dilute solutions, including de-ionized water and raw water from Yangtze River, were presented in dark chlorination and ultraviolet (UV)/chlorination processes. And the effects of initial pH, initial concentration of NaOCl, and UV light intensity on bromate formation in UV/chlorination of the diluted solutions were investigated. Detectable bromate was formed in dark chlorination of the two water samples with a relatively slow production rate. Under routine disinfecting conditions, the amount of formed bromate is not likely to exceed the national standards (10 μg/L). UV irradiation enhanced the decay of free chlorine, and,simultaneously, 6.6%-32% of Br- was oxidized to BrO3-. And the formation of bromate exhibited three stages: rapid stage, slow stage and plateau. Under the experimental conditions (pH = 4.41-11.07, CCl2= 1.23-4.50 mg/L), low pH and high chlorine concentration favored the generation of bromate. High light intensity promoted the production rate of bromate, but decreased its total generation amount due to acceleration of chlorine decomposition.

  10. Chlorine dioxide treatment for zebra mussel control

    Energy Technology Data Exchange (ETDEWEB)

    Rybarik, D. [Dairyland Power Cooperative, La Crosse, WI (United States); Byron, J. [Nalco Chemical Company, Naperville, IL (United States); Germer, M. [Rio Linda Chemical Company, Sacramento, CA (United States)

    1995-06-01

    Chlorine is recognized and commonly used biocide for power plant cooling water and service water treatment programs, including the control of zebra mussels. Chlorine dioxide has recently become a popular method of zebra mussel control because of its economy, safety, environmental acceptability, and effectiveness when compared to other mussel control methods. This control technique was recently demonstrated at Dairyland Power Cooperative`s Alma Generating Station on the east bank of the upper Mississippi River in Alma, Wisconsin. The project was assisted with EPRI Tailored Collaboration Program funds. The Dairyland Power Alam Generating Station consists of five generating units that utilize raw, untreated Mississippi River water for condenser, circulating, and service water supplies. The first units were built in 1947, with the final and largest unit being completed in 1960. Total station generating capacity is 200 MW. Because of recent increases in the zebra mussel density at the station intake, Dairyland Power selected the team of Nalco and Rio Linda to perform a chlorine dioxide treatment of the station`s new water systems to eradicate and control the mussels before their presence created operational difficulties. This paper will present the results of the treatment including treatment theory, design and construction of the treatment system, the method of chlorine dioxide generation, treatment concentration, analytical methods o monitoring chlorine dioxide generation, residuals and trihalomethane (THM) concentrations, protocol for monitoring treatment mortality, and the effects of chlorine dioxide and detoxification on other water chemistry parameters and equipment materials. The goal of this paper is to inform and assist users with establishing consistent and uniform practices for safely utilizing and monitoring chlorine dioxide in the eradication and control of zebra mussels.

  11. Influencing factors and degradation products of antipyrine chlorination in water with free chlorine

    Institute of Scientific and Technical Information of China (English)

    Meiquan Cai; Liqiu Zhang; Fei Qi; Li Feng

    2013-01-01

    Owing to its low cost,free chlorine is one of the most common disinfectants for wastewater and drinking water treatment.However,the formation of disinfection byproducts has been found to occur after free chlorine disinfection in recent decades.Antipyrine (ANT),an anti-inflammatory analgesic,has been frequently detected in the aquatic environment.In this work.the removal efficiency of ANT by free chlorine oxidation in ultrapure water was investigated with batch experiments.The influencing factors on the removal of ANT were explored at initial concentrations of ANT from 0.04 to 0.64 mg/L,free chlorine dosage from 0.30 to 1.31 mg/L,and pH from 1.5 to 9.0.The main degradation products were identified by solid phase extraction-gas chromatography-mass spectrometry.The results showed that ANT reacted rapidly with free chlorine in ultrapure water systems and up to 90.6% removal efficiency of ANT was achieved after 25 sec (initial free chlorine 1 mg/L,ANT 0.5 mg/L,pH 7.0).Higher oxidant dosage,lower ANT initial concentration and low pH favor the ANT removal.The main degradation product in ANT chlorination was a monochlorine substitution product (4-chloro-l,2-dihydro1,5-dimethyl-2-phenyl-3H-pyrazol-3-one),which can be further chlorinated by free chlorine.In addition,the total organic carbon result indicated that ANT is difficult to be mineralized using chlorine.

  12. Influencing factors and degradation products of antipyrine chlorination in water with free chlorine.

    Science.gov (United States)

    Cai, Meiquan; Zhang, Liqiu; Qi, Fei; Feng, Li

    2013-01-01

    Owing to its low cost, free chlorine is one of the most common disinfectants for wastewater and drinking water treatment. However, the formation of disinfection byproducts has been found to occur after free chlorine disinfection in recent decades. Antipyrine (ANT), an anti-inflammatory analgesic, has been frequently detected in the aquatic environment. In this work, the removal efficiency of ANT by free chlorine oxidation in ultrapure water was investigated with batch experiments. The influencing factors on the removal of ANT were explored at initial concentrations of ANT from 0.04 to 0.64 mg/L, free chlorine dosage from 0.30 to 1.31 mg/L, and pH from 1.5 to 9.0. The main degradation products were identified by solid phase extraction-gas chromatography-mass spectrometry. The results showed that ANT reacted rapidly with free chlorine in ultrapure water systems and up to 90.6% removal efficiency of ANT was achieved after 25 sec (initial free chlorine 1 mg/L, ANT 0.5 mg/L, pH 7.0). Higher oxidant dosage, lower ANT initial concentration and low pH favor the ANT removal. The main degradation product in ANT chlorination was a monochlorine substitution product (4-chloro-1,2-dihydro-1,5-dimethyl-2-phenyl-3H-pyrazol-3-one), which can be further chlorinated by free chlorine. In addition, the total organic carbon result indicated that ANT is difficult to be mineralized using chlorine.

  13. Persistent Energetic Electrons in Methylammonium Lead Iodide Perovskite Thin Films.

    Science.gov (United States)

    Niesner, Daniel; Zhu, Haiming; Miyata, Kiyoshi; Joshi, Prakriti P; Evans, Tyler J S; Kudisch, Bryan J; Trinh, M Tuan; Marks, Manuel; Zhu, X-Y

    2016-12-07

    In conventional semiconductor solar cells, carriers are extracted at the band edges and the excess electronic energy (E*) is lost as heat. If E* is harvested, power conversion efficiency can be as high as twice the Shockley-Queisser limit. To date, materials suitable for hot carrier solar cells have not been found due to efficient electron/optical-phonon scattering in most semiconductors, but our recent experiments revealed long-lived hot carriers in single-crystal hybrid lead bromide perovskites. Here we turn to polycrystalline methylammonium lead iodide perovskite, which has emerged as the material for highly efficient solar cells. We observe energetic electrons with excess energy ⟨E*⟩ ≈ 0.25 eV above the conduction band minimum and with lifetime as long as ∼100 ps, which is 2-3 orders of magnitude longer than those in conventional semiconductors. The energetic carriers also give rise to hot fluorescence emission with pseudo-electronic temperatures as high as 1900 K. These findings point to a suppression of hot carrier scattering with optical phonons in methylammonium lead iodide perovskite. We address mechanistic origins of this suppression and, in particular, the correlation of this suppression with dynamic disorder. We discuss potential harvesting of energetic carriers for solar energy conversion.

  14. Ionic transport in hybrid lead iodide perovskite solar cells

    Science.gov (United States)

    Eames, Christopher; Frost, Jarvist M.; Barnes, Piers R. F.; O'Regan, Brian C.; Walsh, Aron; Islam, M. Saiful

    2015-01-01

    Solar cells based on organic–inorganic halide perovskites have recently shown rapidly rising power conversion efficiencies, but exhibit unusual behaviour such as current–voltage hysteresis and a low-frequency giant dielectric response. Ionic transport has been suggested to be an important factor contributing to these effects; however, the chemical origin of this transport and the mobile species are unclear. Here, the activation energies for ionic migration in methylammonium lead iodide (CH3NH3PbI3) are derived from first principles, and are compared with kinetic data extracted from the current–voltage response of a perovskite-based solar cell. We identify the microscopic transport mechanisms, and find facile vacancy-assisted migration of iodide ions with an activation energy of 0.6 eV, in good agreement with the kinetic measurements. The results of this combined computational and experimental study suggest that hybrid halide perovskites are mixed ionic–electronic conductors, a finding that has major implications for solar cell device architectures. PMID:26105623

  15. Numerical modelling of methyl iodide in the eastern tropical Atlantic

    Directory of Open Access Journals (Sweden)

    I. Stemmler

    2013-06-01

    Full Text Available Methyl iodide (CH3I is a volatile organic halogen compound that contributes significantly to the transport of iodine from the ocean to the atmosphere, where it plays an important role in tropospheric chemistry. CH3I is naturally produced and occurs in the global ocean. The processes involved in the formation of CH3I, however, are not fully understood. In fact, there is an ongoing debate whether production by phytoplankton or photochemical degradation of organic matter is the main source term. Here, both the biological and photochemical production mechanisms are considered in a biogeochemical module that is coupled to a one-dimensional water column model for the eastern tropical Atlantic. The model is able to reproduce observed subsurface maxima of CH3I concentrations. But, the dominating source process cannot be clearly identified as subsurface maxima can occur due to both direct biological and photochemical production. However, good agreement between the observed and simulated difference between surface and subsurface methyl iodide concentrations is achieved only when direct biological production is taken into account. Production rates for the biological CH3I source that were derived from published laboratory studies are shown to be inappropriate for explaining CH3I concentrations in the eastern tropical Atlantic.

  16. Nuclear detonation, thyroid cancer and potassium iodide prophylaxis

    Directory of Open Access Journals (Sweden)

    Viroj Wiwanitkit

    2011-01-01

    Full Text Available The recent nuclear disaster at Japan has raised global concerns about effects of radioactive leakage in the environment, associated hazards, and how they can be prevented. In this article, we have tried to explain about the guidelines laid down by World Health Organization for a potassium iodide prophylaxis following a nuclear disaster, and its mechanism of action in preventing thyroid cancer. Data was collected mainly from the studies carried out during the Chernobyl disaster of Russia in 1986 and the hazardous effects especially on the thyroid gland were studied. It was seen that radioactive iodine leakage from the nuclear plants mainly affected the thyroid gland, and especially children were at a higher risk at developing the cancers. Potassium Iodide prophylaxis can be administered in order to prevent an increase in the incidence of thyroid cancers in the population of an area affected by a nuclear disaster. However, one has to be cautious while giving it, as using it without indication has its own risks.

  17. Effect of chlorination on the development of marine biofilms dominated by diatoms

    Digital Repository Service at National Institute of Oceanography (India)

    Patil, J.S.; Jagadeesan, V.

    , and Thalassionema did not increase in density after chlorine treatment. It was also demonstrated that diatoms can colonize, grow and photosynthesize on chlorine-treated surfaces. Under pulse chlorination (treatment every 6 h), irrespective of chlorine concentration...

  18. Thyroid hormones and iodide in the near-term pregnant rat.

    NARCIS (Netherlands)

    Versloot, P.M.

    1998-01-01

    Thyroid hormones, thyroxine (T4) and 3,5,3'-triiodothyronine (T3), are produced by the thyroid gland. To synthesize thyroid hormones the thyroid needs iodide. The uptake of iodide as well as the production and secretion of T4 and T3 by the thyroid gland is regulated by thyrotropin (TSH), which is pr

  19. Effects of radiation and temperature on iodide sorption by surfactant-modified bentonite.

    Science.gov (United States)

    Choung, Sungwook; Kim, Minkyung; Yang, Jung-Seok; Kim, Min-Gyu; Um, Wooyong

    2014-08-19

    Bentonite, which is used as an engineered barrier in geological repositories, is ineffective for sorbing anionic radionuclides because of its negatively charged surface. This study modified raw bentonite using a cationic surfactant (i.e., hexadecyltrimethylammonium [HDTMA]-Br) to improve its sorption capability for radioactive iodide. The effects of temperature and radiation on the iodide sorption of surfactant-modified bentonite (SMB) were also evaluated under alkaline pH condition similar to that found in repository environments. Different amounts of surfactant, equivalent to the 50, 100, and 200% cation-exchange capacity of the bentonite, were used to produce the HDTMA-SMB for iodide sorption. The sorption reaction of the SMB with iodide reached equilibrium rapidly within 10 min regardless of temperature and radiation conditions. The rate of iodide sorption increased as the amount of the added surfactant was increased and nonlinear sorption behavior was exhibited. However, high temperature and γ-irradiation ((60)Co) resulted in significantly (∼2-10 times) lower iodide Kd values for the SMB. The results of FTIR, NMR, and XANES spectroscopy analysis suggested that the decrease in iodide sorption may be caused by weakened physical electrostatic force between the HDTMA and iodide, and by the surfactant becoming detached from the SMB during the heating and irradiation processes.

  20. Tungstosilicic Acid: An Efficient and Ecofriendly Catalyst for the Conversion of Alcohols to Alkyl Iodides

    Directory of Open Access Journals (Sweden)

    Masoud Mokhtary

    2011-01-01

    Full Text Available Treatment of a range of benzylic, allylic, and secondary aliphatic alcohols with potassium iodides in the presence of H4SiW12O40 affords the corresponding alkyl iodides in good to excellent yield with straightforward purification at room temperature in CH3CN.

  1. Bibenzimidazole containing mixed ligand cobalt(III) complex as a selective receptor for iodide

    Digital Repository Service at National Institute of Oceanography (India)

    Indumathy, R.; Parameswarana, P.S.; Aiswarya, C.V.; Nair, B.U.

    -, OH- and OAc- do not bring about any dramatic visual colorimetric changes. However, metallo-receptor 2 brings about vivid color change with iodide anion visually and this could be due to charge transfer transition via ion pair formation with iodide ion...

  2. CuI-catalyzed Synthesis of Aryl Thiocyanates from Aryl Iodides

    Institute of Scientific and Technical Information of China (English)

    Ye Feng WANG; Yuan ZHOU; Jia Rui WANG; Lei LIU; Qing Xiang GUO

    2006-01-01

    An operationally simple and inexpensive catalyst system was developed for the cross coupling of potassium thiocyanate with aryl iodides by using CuI as catalyst, 1, 10-phenanthroline as ligand, and tetraethylammonium iodide as activator. The procedure is applicable for the synthesis of diverse aryl thiocyanates without any exotic, poisonous reagents.

  3. Chlorination of organophosphorus pesticides in natural waters.

    Science.gov (United States)

    Acero, Juan L; Benítez, F Javier; Real, Francisco J; González, Manuel

    2008-05-01

    Unknown second-order rate constants for the reactions of three organophosphorus pesticides (chlorpyrifos, chlorfenvinfos and diazinon) with chlorine were determined in the present study, and the influence of pH and temperature was established. It was found that an increase in the pH provides a negative effect on the pesticides degradation rates. Apparent second-order rate constants at 20 degrees C and pH 7 were determined to be 110.9, 0.004 and 191.6 M(-1) s(-1) for chlorpyrifos, chlorfenvinfos and diazinon, respectively. A higher reactivity of chlorine with the phosphorothioate group (chlorpyrifos and diazinon) than with the phosphate moiety (chlorfenvinfos) could explain these results. Intrinsic rate constant for the elementary reactions of chlorine species with chlorpyrifos and diazinon were also calculated, leading to the conclusion that the reaction between hypochlorous acid and the pesticide is predominant at neutral pH. The elimination of these pesticides in surface waters was also investigated. A chlorine dose of 2.5 mg L(-1) was enough to oxidize chlorpyrifos and diazinon almost completely, with a formation of trihalomethanes below the EU standard for drinking water. However, the removal of chlorfenvinfos was not appreciable. Therefore, chlorination is a feasible option for the removal of organophosphorus pesticides with phosphorothioate group during oxidation and disinfection processes, but not for the elimination of pesticides with phosphate moiety.

  4. Determination of Trace Iodide in Sodium Bisulfite Aqueous Solution by Ion Chromatography with UV Detection

    Energy Technology Data Exchange (ETDEWEB)

    Park, Y.S.; Kim, D.Y.; Choi, K.S.; Park, S.D.; Han, S.H. [Korea Atomic Energy Research Institute, Taejon (Korea)

    2000-06-01

    The iodide was recovered from a simulated spent fuel to the sodium bisulfite aqueous solution. It was discussed that the trace iodide (below 1 ppm) was determined without the matrix effect of 0.1 M sodium bisulfite and 1 mM HNO{sub 3} in aqueous solution by ion chromatography with UV detection. AS4A-SC(DIONEX) column and UV-absorption spectrophotometer were used. The UV-absorption spectra of sodium bisulfite nitric acid and iodide were obtained, and then 230 nm was selected as an absorption wavelength for iodide determination. 0.1 M NaCl eluent was optimum condition. In this condition the calibration curve of iodide was obtained on the range of about 0-1,000 ppb. The linear coefficient was 0.99993 and the detection limit was 5 ppb. The relative standard deviation was 1.26%. (author). 17 refs., 3 tabs., 4 figs.

  5. The Determination of Iodide Based on a Flow-injection Coupling Irreversible Biamperometry

    Institute of Scientific and Technical Information of China (English)

    Li Jun LI; Hao CHENG; Wen Yi HUANG; Hong Xing KONG; Jian Ling WU; Jian Ping LU; Wei GAO; Jun Feng SONG

    2005-01-01

    A novel flow-injection irreversible biamperometric method is described for the direct determination of iodide. The method is based on electrochemical oxidation of iodide at the gold electrode and the reduction of permanganate at the platinum electrode to form an irreversible biamperometric detection system. Under the applied potential difference of 0 V, in the 0.05mol/L sulfuric acid, iodide can be determined over the range 4.00×10-7-l.00×l0-5 mol/L with a sampling frequency of 120 samples per hour. The detection limit for Ⅰ- is 3.0× 10-7 mol/L and the RSD for 40 replicate determinations of 4.0×10-5 mol/L potassium iodide is 1.68%. The new method was applied to the analysis of iodide in table salt with satisfactory results.

  6. Synthesis, growth, structural, thermal, optical properties of new metal-organic crystals: Methyltriphenylphosphonium iodide thiourea and methyltriphenylphosphonium iodide chloroform hemisolvate

    Science.gov (United States)

    Shivachev, Boris L.; Kossev, Krassimir; Dimowa, Louiza T.; Yankov, Georgi; Petrov, Todor; Nikolova, Rositsa P.; Petrova, Nadia

    2013-08-01

    Crystals of methyltriphenylphosphonium iodide thiourea (1) and methyltriphenylphosphonium iodide chloroform hemisolvate (2) were obtained for the first time. Fourier transform infrared (FTIR) spectral studies have been performed to identify the functional groups. Thermogravimetric analysis (TGA) and differential thermal analysis (DTA) were used to study their thermal properties. The optical transmittance window and the lower cutoff wavelength have been identified by UV-vis studies. Crystals of the title compounds suitable for single crystal X-ray analyses were successfully grown by slow evaporation and diffraction data were collected to elucidate the molecular structure and interactions. The proton donors (phosphonium) and proton acceptor (iodine) in the structure of 1 provide infrastructure to introduce charge asymmetry while in 2 chloroform molecule is not involved in the charge transfer. An optical quality crystal of 1 (5×4×2 mm3) was obtained by macroseeding. The crystal has developed facets with major ones (001) and (00¯1). A crystal of 1 was tested with 1060 nm laser radiation and showed second harmonic generation (SHG).

  7. Fabrication of Efficient Low-Bandgap Perovskite Solar Cells by Combining Formamidinium Tin Iodide with Methylammonium Lead Iodide

    Energy Technology Data Exchange (ETDEWEB)

    Liao, Weiqiang; Zhao, Dewei; Yu, Yue; Shrestha, Niraj; Ghimire, Kiran; Grice, Corey R.; Wang, Changlei; Xiao, Yuqing; Cimaroli, Alexander J.; Ellingson, Randy J.; Podraza, Nikolas J.; Zhu, Kai; Xiong, Ren-Gen; Yan, Yanfa

    2016-09-28

    Mixed tin (Sn)-lead (Pb) perovskites with high Sn content exhibit low bandgaps suitable for fabricating the bottom cell of perovskite-based tandem solar cells. In this work, we report on the fabrication of efficient mixed Sn-Pb perovskite solar cells using precursors combining formamidinium tin iodide (FASnI3) and methylammonium lead iodide (MAPbI3). The best-performing cell fabricated using a (FASnI3)0.6(MAPbI3)0.4 absorber with an absorption edge of ~1.2 eV achieved a power conversion efficiency (PCE) of 15.08 (15.00)% with an open-circuit voltage of 0.795 (0.799) V, a short-circuit current density of 26.86(26.82) mA/cm2, and a fill factor of 70.6(70.0)% when measured under forward (reverse) voltage scan. The average PCE of 50 cells we have fabricated is 14.39 +/- 0.33%, indicating good reproducibility.

  8. The effects of low level chlorination and chlorine dioxide on biofouling control in a once-through service water system

    Energy Technology Data Exchange (ETDEWEB)

    Garrett, W.E. Jr. [Alabama Power Co./GSC No. 8, Birmingham, AL (United States); Laylor, M.M. [Univ. of Alabama, Birmingham, AL (United States)

    1995-06-01

    Continuous chlorination has been successfully used for the control of Corbicula at a nuclear power plant located on the Chattahoochee River in southeastern Alabama, since 1986. The purpose of this study was to investigate further minimization of chlorine usage and determine if chlorine dioxide is a feasible alternative. Four continuous biocide treatments were evaluated for macro and microfouling control effectiveness, operational feasibility, and environmental acceptability. One semi-continuous chlorination treatment was also evaluated for macrofouling control effectiveness. Higher treatment residuals were possible with chlorine dioxide than with chlorination due to the river discharge limitations. At the levels tested, continuous chlorine dioxide was significantly more effective in providing both macro and microfouling control. Semi-continuous chlorination was just as effective as continuous chlorination for controlling macrofouling. The Corbicula treatment programs that were tested should all provide sufficient control for zebra mussels. Chlorine dioxide was not as cost effective as chlorination for providing macrofouling control. The semi-continuous treatment save 50% on chemical usage and will allow for the simultaneous treatment of two service water systems. Chlorite levels produced during the chlorine dioxide treatments were found to be environmentally acceptable. Levels of trihalomethanes in the chlorinated service water were less than the maximum levels allowed in drinking water.

  9. Microbiological aspects of the removal of chlorinated hydrocarbons from air

    NARCIS (Netherlands)

    Dolfing, Jan; Wijngaard, Arjan J. van den; Janssen, Dick B.

    1993-01-01

    Chlorinated hydrocarbons are widely used synthetic chemicals that are frequently present in industrial emissions. Bacterial degradation has been demonstrated for several components of this class of compounds. Structural features that affect the degradability include the number of chlorine atoms and

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

    DEFF Research Database (Denmark)

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

    2013-01-01

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

  11. Identification of intermediates leading to chloroform and C-4 diacids in the chlorination of humic acid

    NARCIS (Netherlands)

    Sinninghe Damsté, J.S.; Leer, E.W.B. de; Erkelens, Corrie; Galan, L.

    1985-01-01

    The chlorination of terrestrial humic acid was studied at pH 7. 2 with varying chlorine to carbon ratios. The principal products are chloroform, di- and trichloroacetic acid, and chlorinated C-4 diacids. At a high chlorine dose many new chlorination products were detected, among them chlorinated aro

  12. Horizontal Ampoule Growth and Characterization of Mercuric Iodide at Controlled Gas Pressures for X-Ray and Gamma Ray Spectrometers

    Energy Technology Data Exchange (ETDEWEB)

    McGregor, Douglas S. [Kansas State Univ., Manhattan, KS (United States). Semiconductor Materials and Radiological Technologies Lab., Dept. of Nuclear and Mechanical Engineering; Ariesanti, Elsa [Kansas State Univ., Manhattan, KS (United States). Semiconductor Materials and Radiological Technologies Lab., Dept. of Nuclear and Mechanical Engineering; Corcoran, Bridget [Kansas State Univ., Manhattan, KS (United States). Semiconductor Materials and Radiological Technologies Lab., Dept. of Nuclear and Mechanical Engineering

    2004-04-30

    The project developed a new method for producing high quality mercuric iodide crystals of x-ray and gamma spectrometers. Included are characterization of mercuric iodide crystal properties as a function of growth environment and fabrication and demonstration of room-temperature-operated high-resolution mercuric iodide spectrometers.

  13. Diurnal variation of stratospheric chlorine monoxide - A critical test of chlorine chemistry in the ozone layer

    Science.gov (United States)

    Solomon, P. M.; De Zafra, R.; Parrish, A.; Barrett, J. W.

    1984-01-01

    Ground-based observations of a mm-wave spectral line at 278 GHz have yielded stratospheric chlorine monoxide column density diurnal variation records which indicate that the mixing ratio and column density of this compound above 30 km are about 20 percent lower than model predictions based on 2.1 parts/billion of total stratospheric chlorine. The observed day-to-night variation is, however, in good agreement with recent model predictions, both confirming the existence of a nighttime reservoir for chlorine and verifying the predicted general rate of its storage and retrieval.

  14. Chlorine: Undergraduate Research on an Element of Controversy

    Science.gov (United States)

    Chang, Hasok

    2009-04-01

    If chemical elements were people, chlorine would be a celebrity. Although intrinsically no more or less important than any other element, chlorine has had a knack of making headlines. The genre of "object biography" has been quite successful in popular science recently. We took this opportunity to write a "biographical" study of chlorine. Chlorine's wide range of interesting controversies is well suited for attracting and maintaining the enthusiasm of the diverse range of students we teach in our department.

  15. Determination of chlorine in silicate rocks

    Science.gov (United States)

    Peck, L.C.

    1959-01-01

    In a rapid accurate method for the determination of chlorine in silicate rocks, the rock powder is sintered with a sodium carbonate flux containing zinc oxide and magnesium carbonate. The sinter cake is leached with water, the resulting solution is filtered, and the filtrate is acidified with nitric acid. Chlorine is determined by titrating this solution with mercuric nitrate solution using sodium nitroprusside as the indicator. The titration is made in the dark with a beam of light shining through the solution. The end point of the titration is found by visually comparing the intensity of this beam of light with that of a similar beam of light in a reference solution.

  16. Forcing of Turing patterns in the chlorine dioxide-iodine-malonic acid reaction with strong visible light.

    Science.gov (United States)

    Nagao, Raphael; Epstein, Irving R; Dolnik, Milos

    2013-09-26

    We investigate the sensitivity of Turing patterns in the chlorine dioxide-iodine-malonic acid reaction to illumination by strong white light. Intense illumination results in an increase of [I(-)], in contrast to previous studies, which found only decreased [I(-)] for weak and intermediate intensities of illumination. We propose an expanded mechanism to explain the experimental observations. Both experimental and numerical results suggest that [ClO2] is the key parameter that determines whether the high iodide state is obtained under strong illumination. When strong illumination is applied through a spatially periodic mask with black and white stripes, a dark state with high [I(-)] is produced in the illuminated domain and a light state with low [I(-)] forms in the nonilluminated domain. Depending on the black:white ratio of the mask and its wavelength, Turing patterns can coexist with either the light or the dark state in the nonilluminated domain.

  17. Morphological effects in the quantum yield of cesium iodide

    Energy Technology Data Exchange (ETDEWEB)

    Almeida, J. [Ecole Politechnique Federale, Lausanne (Switzerland). DP-IPA PH-Ecublens; Barbo, F. [Sincrotrone Trieste SpA, Padriciano 99, 34012 Trieste (Italy); Bertolo, M. [Sincrotrone Trieste SpA, Padriciano 99, 34012 Trieste (Italy); Bianco, A. [Sincrotrone Trieste SpA, Padriciano 99, 34012 Trieste (Italy); Braem, A. [European Organization for Nuclear Research, Geneva (Switzerland). Div. Particle Physics Experiments; Cerasari, S. [Sincrotrone Trieste SpA, Padriciano 99, 34012 Trieste (Italy); Coluzza, C. [Ecole Politechnique Federale, Lausanne (Switzerland). DP-IPA PH-Ecublens; Dell`Orto, T. [Ecole Politechnique Federale, Lausanne (Switzerland). DP-IPA PH-Ecublens; Fontana, S. [Sincrotrone Trieste SpA, Padriciano 99, 34012 Trieste (Italy); Margaritondo, G. [Ecole Politechnique Federale, Lausanne (Switzerland). DP-IPA PH-Ecublens; Nappi, E. [Istituto Nazionale di Fisica Nucleare, Bari (Italy); Paic, G. [European Organization for Nuclear Research, Geneva (Switzerland). Div. Particle Physics Experiments; Piuz, F. [European Organization for Nuclear Research, Geneva (Switzerland). Div. Particle Physics Experiments; Sanjines, R. [Ecole Politechnique Federale, Lausanne (Switzerland). DP-IPA PH-Ecublens; Scognetti, T. [Istituto Nazionale di Fisica Nucleare, Bari (Italy); Sgobba, S. [European Organization for Nuclear Research, Geneva (Switzerland). Div. Particle Physics Experiments

    1995-07-15

    We demonstrated that polycrystalline cesium iodide (CsI) on large area Ni/Au coated printed board provides a quantum efficiency (QE) higher by a factor of 2 than the films deposited on the standard Cu/Au printed circuits. This is the most important result of the present systematic study of the QE lateral inhomogeneity for CsI on different substrates. We found a strong correlation between the QE lateral variation and the morphological homogeneity of the films. The QE was measured by UV photoelectron emission microscopy and spatially resolved X-ray photoemission, and the morphology studies were performed by secondary electron microscopy, X-ray diffraction and scanning tunneling microscopy. (orig.).

  18. Electronic characterization of mercuric iodide gamma ray spectrometers

    Energy Technology Data Exchange (ETDEWEB)

    Gerrish, V.M.

    1993-01-01

    During the past four years the yield of high resolution mercuric iodide (HgI[sub 2]) gamma ray spectrometers produced at EG G/EM has increased dramatically. Data is presented which demonstrates a strong correlation between starting material and spectrometer performance. Improved spectrometer yields are attributed to the method of HgI[sub 2] synthesis and to material purification procedures. Data is presented which shows that spectrometer performance is correlated with hole mobility-lifetime products. In addition, the measurement of Schottky barrier heights on HgI[sub 2] spectrometers has been performed using I-V curves and the photoelectric method. Barrier heights near 1.1 eV have been obtained using various contacts and contact deposition methods. These data suggest the pinning of the Fermi level at midgap at the HgI[sub 2] surface, probably due to surface states formed prior to contact deposition.

  19. Electronic characterization of mercuric iodide gamma ray spectrometers

    Energy Technology Data Exchange (ETDEWEB)

    Gerrish, V.M.

    1993-06-01

    During the past four years the yield of high resolution mercuric iodide (HgI{sub 2}) gamma ray spectrometers produced at EG&G/EM has increased dramatically. Data is presented which demonstrates a strong correlation between starting material and spectrometer performance. Improved spectrometer yields are attributed to the method of HgI{sub 2} synthesis and to material purification procedures. Data is presented which shows that spectrometer performance is correlated with hole mobility-lifetime products. In addition, the measurement of Schottky barrier heights on HgI{sub 2} spectrometers has been performed using I-V curves and the photoelectric method. Barrier heights near 1.1 eV have been obtained using various contacts and contact deposition methods. These data suggest the pinning of the Fermi level at midgap at the HgI{sub 2} surface, probably due to surface states formed prior to contact deposition.

  20. Dual frequency cavitation event sensor with iodide dosimeter.

    Science.gov (United States)

    Ebrahiminia, Ali; Mokhtari-Dizaji, Manijhe; Toliyat, Tayebeh

    2016-01-01

    The inertial cavitation activity depends on the sonication parameters. The purpose of this work is development of dual frequency inertial cavitation meter for therapeutic applications of ultrasound waves. In this study, the chemical effects of sonication parameters in dual frequency sonication (40 kHz and 1 MHz) were investigated in the progressive wave mode using iodide dosimetry. For this purpose, efficacy of different exposure parameters such as intensity, sonication duration, sonication mode, duty factor and net ultrasound energy on the inertial cavitation activity have been studied. To quantify cavitational effects, the KI dosimeter solution was sonicated and its absorbance at a wavelength of 350 nm was measured. The absorbance values in continuous sonication mode was significantly higher than the absorbance corresponding to the pulsed mode having duty factors of 20-80% (plevel intensity (sensor can be useful for ultrasonic treatments.

  1. Development of mercuric iodide detectors for XAS and XRD measurements

    Energy Technology Data Exchange (ETDEWEB)

    Warburton, W.K.; Iwanczyk, J.S.; Dabrowski, A.J.; Hedman, B.; Penner-Hakn, J.E.; Roe, A.L.; Hodgson, K.O.; Beyerle, A.

    1985-07-01

    A prototype element for an energy dispersive detector (EDD) array was constructed using a Mercuric Iodide detector. Both detector and front end FET could be thermoelectrically cooled. Tested at SSRL, the detector had 250 eV electronic noise and 315 eV resolution at 5.9 keV. K line fluorescence spectra were collected for selected elements between Cl (2622 eV) and Zn (8638 eV). Count rate capability to 60,000 cps was demonstrated. Several detector parameters were measured, including energy linearity, resolution vs. shaping time, and detector dead time. An EXAFS (extended x-ray absorption fine structure) spectrum was recorded and compared to simultaneously collected transmission data.

  2. Radiative efficiency of lead iodide based perovskite solar cells

    Science.gov (United States)

    Tvingstedt, Kristofer; Malinkiewicz, Olga; Baumann, Andreas; Deibel, Carsten; Snaith, Henry J.; Dyakonov, Vladimir; Bolink, Henk J.

    2014-08-01

    The maximum efficiency of any solar cell can be evaluated in terms of its corresponding ability to emit light. We herein determine the important figure of merit of radiative efficiency for Methylammonium Lead Iodide perovskite solar cells and, to put in context, relate it to an organic photovoltaic (OPV) model device. We evaluate the reciprocity relation between electroluminescence and photovoltaic quantum efficiency and conclude that the emission from the perovskite devices is dominated by a sharp band-to-band transition that has a radiative efficiency much higher than that of an average OPV device. As a consequence, the perovskite have the benefit of retaining an open circuit voltage ~0.14 V closer to its radiative limit than the OPV cell. Additionally, and in contrast to OPVs, we show that the photoluminescence of the perovskite solar cell is substantially quenched under short circuit conditions in accordance with how an ideal photovoltaic cell should operate.

  3. Chlorination of nickel ore by gaseous chlorine in the presence of active additives

    Directory of Open Access Journals (Sweden)

    Ilić Ilija B.

    2003-01-01

    Full Text Available Paper presents a thermodynamic analysis of chemical reactions occurring during chlorination with and without additives for both nickel oxides and nickel ferrites, which are component parts of nickel ore. The experimental research investigated the influence of temperature in the range from 600 up to 1000 °C and time (up to 3 h on the chlorination degree of nickel ores with and without additives. It was found that the introduction of additives such as C, S, BaS and NaCl intensified the chlorination of nickel ore. The results can be applied and may help determine the optimal conditions for the chlorination of low-grade ferrous nickel ores.

  4. Cellular Response of the Amoeba Acanthamoeba castellanii to Chlorine, Chlorine Dioxide, and Monochloramine Treatments ▿

    OpenAIRE

    Mogoa, Emerancienne; Bodet, Charles; Morel, Franck; Rodier, Marie-Hélène; Legube, Bernard; Héchard, Yann

    2011-01-01

    Acanthamoeba castellanii is a free-living amoebae commonly found in water systems. Free-living amoebae might be pathogenic but are also known to bear phagocytosis-resistant bacteria, protecting these bacteria from water treatments. The mode of action of these treatments is poorly understood, particularly on amoebae. It is important to examine the action of these treatments on amoebae in order to improve them. The cellular response to chlorine, chlorine dioxide, and monochloramine was tested o...

  5. Chlorinated organic compounds in urban river sediments

    Energy Technology Data Exchange (ETDEWEB)

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

    1995-12-31

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

  6. Method and apparatus for producing chlorine dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Santillie, P.W.; Ramras, D.M.

    1984-05-29

    A continuous method and apparatus are described for the efficient production of gaseous chlorine dioxide by the reaction between gaseous sulfur dioxide and an aqueous solution of a metallic chlorate. The chlorate solution and a highly concentrated sulfur dioxide gas are introduced into a packed columnar chamber at closely adjacent locations at the bottom of the chamber so as to flood the chamber and maximize both the contact area and contact time of the two reactants. Throughout the reaction the chamber is subjected to high vacuum imposed by an eductor which exhausts the chlorine dioxide gas and spent reactants. For use of the chlorine dioxide to produce potable water or treat foodstuffs, the chlorine dioxide and spent reactants are exhausted from the chamber separately by respective eductors substantially balanced with respect to each other to impose comparable vacuums upon the chamber. Because of the high efficency of the reaction, substantial heat is generated therefrom which is absorbed by a coolant flowing through a jacket surrounding the chamber. The flow rate of the coolant and flow rate of the reactants into the chamber are porportional due to the dependency of the reactant flow rate on the coolant flow rate.

  7. Photoabsorption and photoionization of chlorine dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Flesch, R.; Ruehl, E.; Hottmann, K.; Baumgaertel, H. (Freie Universitaet Berlin (Germany))

    1993-01-28

    Photoprocesses of chlorine dioxide in the near-UV have become highly important for stratospheric photoprocesses at high latitudes, especially in Antarctica. Chlorine dioxide has been identified among other absorbers because of its specific absorption cross section in the near-UV. Possible contributions of chlorine dioxide photochemistry to polar ozone depletion have been discussed recently. The high-resolution He I photoelectron spectrum and the absolute (vacuum-UV) absorption cross section (6-25 eV) as well as the ionic fragmentation of chlorine dioxide (OCIO) are reported. The photoelectron spectrum is interpreted in terms of exchange splitting effects of the various singlet and triplet cation states as well as by comparison to chemically related molecules. The vacuum-UV absorption spectrum shows different Rydberg series converging to the cation states. These Rydberg series and their vibrational progressions are assigned by term value arguments, dipole selection rules, and comparison with the photoelectron spectrum. Photoionization mass spectrometry is used for measurements of the ionization and fragmentation threshold of OCIO. The major fragment is ClO[sup +] which occurs above 13.4 eV. Thermomechanical data such as heats of formation and bond dissociation energies are derived. No evidence for isomerization of OClO[sup +] is found, as observed for the electronically excited neutral molecule. 54 refs., 6 figs., 7 tabs.

  8. Inhibitor treatment program for chlorine dioxide corrosion

    Energy Technology Data Exchange (ETDEWEB)

    Edmondson, J.G.; Holder, E.P.

    1991-11-12

    This patent describes a method of inhibiting corrosion by chlorine dioxide in oil field waterflood systems by adding a sufficient amount of a corrosion inhibiting composition. It comprises a phosphonate, a copolymer consisting of repeating units of acrylic acid/allyl hydroxy propyl sulfonate ether, and a permangante.

  9. Development of w/o microemulsion for transdermal delivery of iodide ions.

    Science.gov (United States)

    Lou, Hao; Qiu, Ni; Crill, Catherine; Helms, Richard; Almoazen, Hassan

    2013-03-01

    The objective of this study was to develop a water-in-oil (w/o) microemulsion which can be utilized as a transdermal delivery for iodide ions. Several w/o microemulsion formulations were prepared utilizing Span 20, ethanol, Capryol 90®, and water. The selected formulations had 5%, 10%, 15%, 20%, and a maximum of 23% w/w water content. Potassium iodide (KI) was incorporated in all formulations at 5% w/v. Physicochemical characterizations were conducted to evaluate the structure and stability. These studies included: mean droplet size, pH, viscosity, conductivity, and chemical stability tests. In vitro human skin permeation studies were conducted to evaluate the diffusion of the iodide ion through human skin. The w/o microemulsion formulations were stable and compatible with iodide ions with water content ranging from 5% to 23% w/w. The addition of KI influenced the physicochemical properties of microemulsion as compared to blank microemulsion formulations. In vitro human skin permeation studies indicated that selected formulations improved iodide ion diffusion significantly as compared to control (KI solution; P valueIodide ions were entrapped within the aqueous core of w/o microemulsion. Span 20, ethanol and Capryol 90 protected the iodide ions against oxidation and formed a stable microemulsion. It is worth to note that according to Hofmeister series, iodide ions tend to lower the interfacial tension between water and oil and consequently enhance overall stability. This work illustrates that microemulsion system can be utilized as a vehicle for the transdermal administration of iodide.

  10. Halogenase-Inspired Oxidative Chlorination Using Flavin Photocatalysis.

    Science.gov (United States)

    Hering, Thea; Mühldorf, Bernd; Wolf, Robert; König, Burkhard

    2016-04-18

    Chlorine gas or electropositive chlorine reagents are used to prepare chlorinated aromatic compounds, which are found in pharmaceuticals, agrochemicals, and polymers, and serve as synthetic precursors for metal-catalyzed cross-couplings. Nature chlorinates with chloride anions, FAD-dependent halogenases, and O2 as the oxidant. A photocatalytic oxidative chlorination is described based on the organic dye riboflavin tetraacetate mimicking the enzymatic process. The chemical process allows within the suitable arene redox potential window a broader substrate scope compared to the specific activation in the enzymatic binding pocket.

  11. Kinetic models and pathways of ronidazole degradation by chlorination, UV irradiation and UV/chlorine processes.

    Science.gov (United States)

    Qin, Lang; Lin, Yi-Li; Xu, Bin; Hu, Chen-Yan; Tian, Fu-Xiang; Zhang, Tian-Yang; Zhu, Wen-Qian; Huang, He; Gao, Nai-Yun

    2014-11-15

    Degradation kinetics and pathways of ronidazole (RNZ) by chlorination (Cl2), UV irradiation and combined UV/chlorine processes were investigated in this paper. The degradation kinetics of RNZ chlorination followed a second-order behavior with the rate constants calculated as (2.13 ± 0.15) × 10(2) M(-2) s(-1), (0.82 ± 0.52) × 10(-2) M(-1) s(-1) and (2.06 ± 0.09) × 10(-1) M(-1) s(-1) for the acid-catalyzed reaction, as well as the reactions of RNZ with HOCl and OCl(-), respectively. Although UV irradiation degraded RNZ more effectively than chlorination did, very low quantum yield of RNZ at 254 nm was obtained as 1.02 × 10(-3) mol E(-1). RNZ could be efficiently degraded and mineralized in the UV/chlorine process due to the generation of hydroxyl radicals. The second-order rate constant between RNZ and hydroxyl radical was determined as (2.92 ± 0.05) × 10(9) M(-1) s(-1). The degradation intermediates of RNZ during the three processes were identified with Ultra Performance Liquid Chromatography - Electrospray Ionization - mass spectrometry and the degradation pathways were then proposed. Moreover, the variation of chloropicrin (TCNM) and chloroform (CF) formation after the three processes were further evaluated. Enhanced formation of CF and TCNM precursors during UV/chlorine process deserves extensive attention in drinking water treatment.

  12. Turbidity and chlorine demand reduction using alum and moringa flocculation before household chlorination in developing countries.

    Science.gov (United States)

    Preston, Kelsey; Lantagne, Daniele; Kotlarz, Nadine; Jellison, Kristen

    2010-03-01

    Over 1.1 billion people in the world lack access to improved drinking water. Diarrhoeal and other waterborne diseases cause an estimated 1.87 million deaths per year. The Safe Water System (SWS) is a household water treatment intervention that reduces diarrhoeal disease incidence among users in developing countries. Turbid waters pose a particular challenge to implementation of SWS programmes; although research shows that a 3.75 mg l(-1) sodium hypochlorite dose effectively treats turbid waters, users sometimes object to the strong chlorine taste and prefer to drink water that is more aesthetically pleasing. This study investigated the efficacy of two locally available chemical water treatments-alum and Moringa oleifera flocculation-to reduce turbidity and chlorine demand at turbidities of 10, 30, 70, 100 and 300 NTU. Both treatments effectively reduced turbidity (alum flocculation 23.0-91.4%; moringa flocculation 14.2-96.2%). Alum flocculation effectively reduced chlorine demand compared with controls at 30, 70, 100 and 300 NTU (p=0.01-0.06). Moringa flocculation increased chlorine demand to the point where adequate free chlorine residual was not maintained for 24 hours after treatment. Alum pretreatment is recommended in waters>or=30 NTU for optimum water disinfection. Moringa flocculation is not recommended before chlorination.

  13. Oxidative elimination of cyanotoxins: comparison of ozone, chlorine, chlorine dioxide and permanganate.

    Science.gov (United States)

    Rodríguez, Eva; Onstad, Gretchen D; Kull, Tomas P J; Metcalf, James S; Acero, Juan L; von Gunten, Urs

    2007-08-01

    As the World Health Organization (WHO) progresses with provisional Drinking Water Guidelines of 1 microg/L for microcystin-LR and a proposed Guideline of 1 microg/L for cylindrospermopsin, efficient treatment strategies are needed to prevent cyanotoxins such as these from reaching consumers. A kinetic database has been compiled for the oxidative treatment of three cyanotoxins: microcystin-LR (MC-LR), cylindrospermopsin (CYN), and anatoxin-a (ANTX) with ozone, chlorine, chlorine dioxide and permanganate. This kinetic database contains rate constants not previously reported and determined in the present work (e.g. for permanganate oxidation of ANTX and chlorine dioxide oxidation of CYN and ANTX), together with previously published rate constants for the remaining oxidation processes. Second-order rate constants measured in pure aqueous solutions of these toxins could be used in a kinetic model to predict the toxin oxidation efficiency of ozone, chlorine, chlorine dioxide and permanganate when applied to natural waters. Oxidants were applied to water from a eutrophic Swiss lake (Lake Greifensee) in static-dose testing and dynamic time-resolved experiments to confirm predictions from the kinetic database, and to investigate the effects of a natural matrix on toxin oxidation and by-product formation. Overall, permanganate can effectively oxidize ANTX and MC-LR, while chlorine will oxidize CYN and MC-LR and ozone is capable of oxidizing all three toxins with the highest rate. The formation of trihalomethanes (THMs) in the treated water may be a restriction to the application of sufficiently high-chlorine doses.

  14. A Direct Transformation of Aryl Aldehydes to Benzyl Iodides Via Reductive Iodination

    Energy Technology Data Exchange (ETDEWEB)

    Ruso, Jayaraman Sembian; Rajendiran, Nagappan; Kumaran, Rajendran Senthil [Univ. of Madras, Chennai (India)

    2014-02-15

    A facile transformation of aryl aldehydes to benzyl iodides through one-pot reductive iodination is reported. This protocol displays remarkable functional group tolerance and the title compound was obtained in good to excellent yield.

  15. Kinetics and mechanism of the mercury(II)-assisted hydrolysis of methyl iodide.

    Science.gov (United States)

    Celo, Valbona; Scott, Susannah L

    2005-04-01

    The kinetics and mechanism of the reaction of aqueous Hg(II) with methyl iodide have been investigated. The overall reaction is best described as Hg(II)-assisted hydrolysis, resulting in quantitative formation of methanol and, in the presence of excess methyl iodide, ultimately, HgI2 via the intermediate HgI+. The kinetics are biexponential when methyl iodide is in excess. At 25 degrees C, the acceleration provided by Hg2+ is 7.5 times greater than that caused by HgI+, while assistance of hydrolysis was not observed for HgI2. Thus, the reactions are not catalytic in Hg(II). The kinetics are consistent with an SN2-M+ mechanism involving electrophilic attack at iodide. As expected, methylation of mercury is not a reaction pathway; traces of methylmercury(II) are artifacts of the extraction/preconcentration procedure used for methylmercury analysis.

  16. Fluorescence characteristics of 5-amino salicylic acid: An iodide recognition study

    Science.gov (United States)

    Arora, Priyanka; Suyal, Kanchan; Joshi, Neeraj K.; Joshi, Hem Chandra; Pant, Sanjay

    In this paper we report the effect of iodide on the fluorescence of 5-amino salicylic acid (5-ASA). In the absence of iodide, prominent blue green (BG) emission band at ˜465 nm (broad) is observed in aprotic solvents whereas violet (V) emission at ˜408 nm, blue green (BG) at ˜480 nm and green (G) at ˜500 nm are observed in case of protic solvents. On the addition of iodide ion (I-), the intensity of BG fluorescence is enhanced in case of aprotic solvents. On the other hand the G band is enhanced in protic solvents and decrease in the intensity of the V band is observed. The effect of hydrogen bonding as well as the interplay of neutral and ionic species is invoked to explain the observed results. The study projects the application of this system in iodide recognition in protic/aprotic environments.

  17. Chlorine hazard evaluation for the zinc-chlorine electric vehicle battery. Final technical report. [50 kWh

    Energy Technology Data Exchange (ETDEWEB)

    Zalosh, R. G.; Bajpai, S. N.; Short, T. P.; Tsui, R. K.

    1980-04-01

    Hazards associated with conceivable accidental chlorine releases from zinc-chlorine electric vehicle batteries are evaluated. Since commercial batteries are not yet available, this hazard assessment is based on both theoretical chlorine dispersion models and small-scale and large-scale spill tests with chlorine hydrate (which is the form of chlorine storage in the charged battery). Six spill tests involving the chlorine hydrate equivalent of a 50-kWh battery indicate that the danger zone in which chlorine vapor concentrations intermittently exceed 100 ppM extends at least 23 m directly downwind of a spill onto a warm (30 to 38/sup 0/C) road surface. Other accidental chlorine release scenarios may also cause some distress, but are not expected to produce the type of life-threatening chlorine exposures that can result from large hydrate spills. Chlorine concentration data from the hydrate spill tests compare favorably with calculations based on a quasi-steady area source dispersion model and empirical estimates of the hydrate decomposition rate. The theoretical dispersion model was combined with assumed hydrate spill probabilities and current motor vehicle accident statistics in order to project expected chlorine-induced fatality rates. These calculations indicate that expected chlorine fataility rates are several times higher in a city such as Los Angeles with a warm and calm climate than in a colder and windier city such as Boston. Calculated chlorine-induced fatality rate projections for various climates are presented as a function of hydrate spill probability in order to illustrate the degree of vehicle/battery crashworthiness required to maintain chlorine-induced fatality rates below current vehicle fatality rates due to fires and asphyxiations. 37 figures, 19 tables.

  18. Comparative efficacy of chlorine and chlorine dioxide regimes for condenser slime control in seawater cooled heat exchangers

    Energy Technology Data Exchange (ETDEWEB)

    Murthy, P.S.; Veeramani, P.; Ershath, M.; Rajamohan, R.; Harinath, Y.V.; Mohan, T.V.K.; Venugopalan, V.P. [BARC Facilities, Water and Steam Chemistry Div., Kalpakkam, Tamil nadu (India)

    2010-07-01

    Chlorination has long been used as an effective and economic biocide for biofouling control in seawater cooling systems. However, the efficacy of chlorine is reduced in the presence of organic content of seawater and the inability of chlorine to effectively penetrate biofilms. Chlorine dioxide is being projected as a possible alternative to chlorine. Experiments were carried out with the help of a seawater circulating facility, in which direct comparison of the efficacy of the two biocides was possible using test condenser tube assemblies. The test condenser tubes made of titanium, SS 316L and Cu-Ni 90/10 were dosed with chlorine and chlorine dioxide. Each dose was evaluated for 30 days. Continuous and intermittent additions of chlorine (0.38 - 0.45 mg L{sup -1} TRO) and chlorine dioxide (0.4 - 0.5 mg L{sup -1}) were used, along with control. The flow velocity in the tubes was maintained at 1.5 m/s. Results of the study showed that the efficacy of the biocide to control biofilms depended on the biocide and the material. Continuous chlorination resulted in 75% reduction of viable counts on titanium, followed by 24% reduction on CuNi and 6% reduction on SS 316L surfaces, as compared to the control. When compared to continuous chlorination, increase in bacterial density in the tubes was observed at different regimes of intermittent chlorination. On SS 316L and Cu-Ni surfaces, intermittent chlorination for 1h, once every 3 h, appeared to give adequate protection. Continuous addition of chlorine dioxide resulted in 99% reduction of viable counts on titanium surfaces, followed by 28% reduction on SS 316 L surfaces and 52% reduction on Cu-Ni surfaces, as compared to the controls. The data indicate that the efficacy of biocides to control biofilms depend on not only the biocide and its frequency of application but also the material of construction. (author)

  19. Horseradish Peroxidase-Mediated, Iodide-Catalyzed Cascade Reaction for Plasmonic Immunoassays.

    Science.gov (United States)

    Xianyu, Yunlei; Chen, Yiping; Jiang, Xingyu

    2015-11-01

    This report outlines an enzymatic cascade reaction for signal transduction and amplification for plasmonic immunoassays by using horseradish peroxidase (HRP)-mediated aggregation of gold nanoparticles (AuNPs). HRP-catalyzed oxidation of iodide and iodide-catalyzed oxidation of cysteine is employed to modulate the plasmonic signals of AuNPs. It agrees well with the current immunoassay platforms and allows naked-eye readout with enhanced sensitivity, which holds great promise for applications in resource-constrained settings.

  20. Air-Driven Potassium Iodide-Mediated Oxidative Photocyclization of Stilbene Derivatives.

    Science.gov (United States)

    Matsushima, Tomoya; Kobayashi, Sayaka; Watanabe, Soichiro

    2016-09-02

    A new method has been developed for the potassium iodide-mediated oxidative photocyclization of stilbene derivatives. Compared with conventional iodine-mediated oxidative photocyclization reactions, this new method requires shorter reaction times and affords cyclized products in yields of 45-97%. This reaction proceeds with a catalytic amount of potassium iodide and works in an air-driven manner without the addition of an external scavenger. The radical-mediated oxidative photocyclization of stilbene derivatives using TEMPO was also investigated.

  1. [Study on the stability of potassium iodide of the iodized salt].

    Science.gov (United States)

    Voudouris, E

    1975-04-29

    The stability of potassium iodide in iodized salt has been studied with respect to the purity of the salt used as raw material. It has been found that the iodized salt prepared from high purity salt and preserved under proper conditions (protection from light, humidity and high temperatures) keeps, for several months, the most of the initially added potassium iodide, without any addition of stabilizers, except for a small bicarbonate.

  2. Permeation of iodide from iodine-enriched yeast through porcine intestine.

    Science.gov (United States)

    Ryszka, Florian; Dolińska, Barbara; Zieliński, Michał; Chyra, Dagmara; Dobrzański, Zbigniew

    2013-01-01

    Iodine deficiency is a common phenomenon, threatening the whole global human population. Recommended daily intake of iodine is 150 μg for adults and 250 μg for pregnant and breastfeeding women. About 50% of human population can be at risk of moderate iodine deficiency. Due to this fact, increased iodine supplementation is recommended, through intake of iodized mineral water and salt iodization. The aim of this study was to investigate permeation and absorption of iodide from iodine bioplex (experimental group) in comparison with potassium iodide (controls). Permeation and absorption processes were investigated in vitro using a porcine intestine. The experimental model was based on a standard Franz diffusion cell (FD-Cell). The iodine bioplex was produced using Saccharomyces cerevisiae yeast and whey powder: iodine content - 388 μg/g, total protein - 28.5%, total fat - 0.9%., glutamic acid - 41.2%, asparaginic acid - 29.4%, lysine - 24.8%; purchased from: F.Z.N.P. Biochefa, Sosnowiec, Poland. Potassium iodide was used as controls, at 388 μg iodine concentration, which was the same as in iodine-enriched yeast bioplex. A statistically significant increase in iodide permeation was observed for iodine-enriched yeast bioplex in comparison with controls - potassium iodide. After 5h the total amount of permeated iodide from iodine-enriched yeast bioplex was 85%, which is ~ 2-fold higher than controls - 37%. Iodide absorption was by contrast statistically significantly higher in controls - 7.3%, in comparison with 4.5% in experimental group with iodine-enriched yeast bioplex. Presented results show that iodide permeation process dominates over absorption in case of iodine-enriched yeast bioplex.

  3. Modelling iodide – iodate speciation in atmospheric aerosol: Contributions of inorganic and organic iodine chemistry

    Directory of Open Access Journals (Sweden)

    S. Pechtl

    2007-01-01

    Full Text Available The speciation of iodine in atmospheric aerosol is currently poorly understood. Models predict negligible iodide concentrations but accumulation of iodate in aerosol, both of which is not confirmed by recent measurements. We present an updated aqueous phase iodine chemistry scheme for use in atmospheric chemistry models and discuss sensitivity studies with the marine boundary layer model MISTRA. These studies show that iodate can be reduced in acidic aerosol by inorganic reactions, i.e., iodate does not necessarily accumulate in particles. Furthermore, the transformation of particulate iodide to volatile iodine species likely has been overestimated in previous model studies due to negligence of collision-induced upper limits for the reaction rates. However, inorganic reaction cycles still do not seem to be sufficient to reproduce the observed range of iodide – iodate speciation in atmospheric aerosol. Therefore, we also investigate the effects of the recently suggested reaction of HOI with dissolved organic matter to produce iodide. If this reaction is fast enough to compete with the inorganic mechanism, it would not only directly lead to enhanced iodide concentrations but, indirectly via speed-up of the inorganic iodate reduction cycles, also to a decrease in iodate concentrations. Hence, according to our model studies, organic iodine chemistry, combined with inorganic reaction cycles, is able to reproduce observations. The presented chemistry cycles are highly dependent on pH and thus offer an explanation for the large observed variability of the iodide – iodate speciation in atmospheric aerosol.

  4. Lead iodide X-ray and gamma-ray spectrometers for room and high temperature operation

    Energy Technology Data Exchange (ETDEWEB)

    Hermon, H.; James, R.B.; Cross, E. [and others

    1997-02-01

    In this study, we report on the results of the investigation of lead iodide material properties. The effectiveness of zone refining purification methods on the material purity is determined by ICP-MS and ICP-OES and correlated to the electrical and physical material properties. We show that this zone refining method is very efficient in removing impurities from lead iodide and we also determine the segregation coefficient for some of these impurities. Triple axis x- ray diffraction (TAD) analysis has been used to determine the crystalline perfection of the lead iodide after applying various cutting, etching, and fabrication methods. The soft lead iodide crystal was found to be damaged when cleaved by a razor blade, but by using a diamond wheel saw, followed by etching, the crystallinity of the material was improved, as observed by TAD. Low temperature photoluminescence also indicates an improvement in the material properties of the purified lead iodide. Electrical properties of lead iodide such as carrier mobility, were calculated based on carrier- phonon scattering. The results for the electrical properties were in good agreement with the experimental data.

  5. Critical evaluation of acetylthiocholine iodide and acetylthiocholine chloride as substrates for amperometric biosensors based on acetylcholinesterase.

    Science.gov (United States)

    Bucur, Madalina-Petruta; Bucur, Bogdan; Radu, Gabriel-Lucian

    2013-01-25

    Numerous amperometric biosensors have been developed for the fast analysis of neurotoxic insecticides based on inhibition of cholinesterase (AChE). The analytical signal is quantified by the oxidation of the thiocholine that is produced enzymatically by the hydrolysis of the acetylthiocholine pseudosubstrate. The pseudosubstrate is a cation and it is associated with chloride or iodide as corresponding anion to form a salt. The iodide salt is cheaper, but it is electrochemically active and consequently more difficult to use in electrochemical analytical devices. We investigate the possibility of using acetylthiocholine iodide as pseudosubstrate for amperometric detection. Our investigation demonstrates that operational conditions for any amperometric biosensor that use acetylthiocholine iodide must be thoroughly optimized to avoid false analytical signals or a reduced sensitivity. The working overpotential determined for different screen-printed electrodes was: carbon-nanotubes (360 mV), platinum (560 mV), gold (370 mV, based on a catalytic effect of iodide) or cobalt phthalocyanine (110 mV, but with a significant reduced sensitivity in the presence of iodide anions).

  6. Stability and electronic properties of two-dimensional indium iodide

    Science.gov (United States)

    Wang, Jizhang; Dong, Baojuan; Guo, Huaihong; Yang, Teng; Zhu, Zhen; Hu, Gan; Saito, Riichiro; Zhang, Zhidong

    2017-01-01

    Based on ab initio density functional calculations, we studied the stability and electronic properties of two-dimensional indium iodide (InI). The calculated results show that monolayer and few-layer InI can be as stable as its bulk counterpart. The stability of the monolayer structure is further supported by examining the electronic and dynamic stability. The interlayer interaction is found to be fairly weak (˜160 meV/atom) and mechanical exfoliation to obtain monolayer and few-layer structures will be applicable. A direct band gap of 1.88 eV of the bulk structure is obtained from the hybrid functional method, and is comparable to the experimental one (˜2.00 eV). The electronic structure can be tuned by layer stacking and external strain. The size of the gap is a linear function of an inverse number of layers, suggesting that we can design few-layer structures for optoelectronic applications in the visible optical range. In-plane tensile or hydrostatic compressive stress is found to be useful not only in varying the gap size to cover the whole visible optical range, but also in inducing a semiconductor-metal transition with an experimentally accessible stress. The present result strongly supports the strategy of broadening the scope of group-V semiconductors by looking for isoelectronic III-VII atomic-layered materials.

  7. Persistent photovoltage in methylammonium lead iodide perovskite solar cells

    Science.gov (United States)

    Baumann, A.; Tvingstedt, K.; Heiber, M. C.; Väth, S.; Momblona, C.; Bolink, H. J.; Dyakonov, V.

    2014-08-01

    We herein perform open circuit voltage decay (OCVD) measurements on methylammonium lead iodide (CH3NH3PbI3) perovskite solar cells to increase the understanding of the charge carrier recombination dynamics in this emerging technology. Optically pulsed OCVD measurements are conducted on CH3NH3PbI3 solar cells and compared to results from another type of thin-film photovoltaics, namely, the two reference polymer-fullerene bulk heterojunction solar cell devices based on P3HT:PC60BM and PTB7:PC70BM blends. We observe two very different time domains of the voltage transient in the perovskite solar cell with a first drop on a short time scale that is similar to the decay in the studied organic solar cells. However, 65%-70% of the maximum photovoltage persists on much longer timescales in the perovskite solar cell than in the organic devices. In addition, we find that the recombination dynamics in all time regimes are dependent on the starting illumination intensity, which is also not observed in the organic devices. We then discuss the potential origins of these unique behaviors.

  8. Structural Effects on the Bandstructure of Methylammonium Lead Iodide

    Science.gov (United States)

    Bernardi, Marco; Barker, Bradford A.; Vigil-Fowler, Derek; Neaton, Jeffrey B.; Louie, Steven G.; Louie Team

    Metal-organic halide perovskites possess peculiar physical properties. The carrier diffusion length in methylammonium lead iodide (MAPbI) exceeds 1 μm, but this unusually high value for a solution-processed material is poorly understood. We developed first-principles calculations of carrier lifetimes and diffusion lengths in semiconductors, which require accurate knowledge of the bandstructure. In this talk, we show that in MAPbI the structure strongly affects the bandstructure and band edges, and that density functional theory (DFT) is unable to predict the room temperature tetragonal structure due to the polymorphism of MAPbI. The Rashba splitting induced by the spin-orbit interaction, and the DFT band gap and effective masses, all depend strongly on the chosen structure, a point that previous work failed to address. Working with multiple stochastic realizations of large unit cells with random methylammonium orientations, we compute average effective masses and show that the effective mass depends linearly on the band gap. The average Rashba coefficient we find is an order of magnitude smaller than previously reported, and the band edges are almost parabolic. Our structures possess the correct symmetry and are free of the spurious Pb off-centering assumed in previous work. We identify the correct starting point for GW bandstructure calculations and to compute the carrier lifetime and diffusion length.

  9. Chloride, bromide and iodide scintillators with europium doping

    Science.gov (United States)

    Zhuravleva, Mariya; Yang, Kan

    2014-08-26

    A halide scintillator material is disclosed where the halide may comprise chloride, bromide or iodide. The material is single-crystalline and has a composition of the general formula ABX.sub.3 where A is an alkali, B is an alkali earth and X is a halide which general composition was investigated. In particular, crystals of the formula ACa.sub.1-yEu.sub.yI.sub.3 where A=K, Rb and Cs were formed as well as crystals of the formula CsA.sub.1-yEu.sub.yX.sub.3 (where A=Ca, Sr, Ba, or a combination thereof and X=Cl, Br or I or a combination thereof) with divalent Europium doping where 0.ltoreq.y.ltoreq.1, and more particularly Eu doping has been studied at one to ten mol %. The disclosed scintillator materials are suitable for making scintillation detectors used in applications such as medical imaging and homeland security.

  10. Revisiting the thermochemistry of chlorine fluorides

    CERN Document Server

    Sánchez, H R

    2016-01-01

    In this work, accurate calculations of standard enthalpies of formation of chlorine fluorides (ClF$_n$, n=1--7; Cl$_2$F and Cl$_3$F$_2$) were performed through the isodesmic reactions scheme. It is argued that, for many chlorine fluorides, the gold standard method of quantum chemistry (CCSD(T)) is not capable to predict enthalpy values nearing chemical accuracy if atomization scheme is used. This is underpinned by a thorough analysis of total atomization energy results and the inspection of multireference features of these compounds. Other thermodynamic quantities were also calculated at different temperatures. In order to complement the energetic description, elimination curves were studied through density functional theory as a computationally affordable alternative to highly correlated wave function-based methods.

  11. Behavioral toxicology, risk assessment, and chlorinated hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Evangelista de Duffard, A.M.; Duffard, R. [Laboratorio de Toxicologia Experimental, Santa Fe (Argentina)

    1996-04-01

    Behavioral end points are being used with greater frequency in neurotoxicology to detect and characterize the adverse effects of chemicals on the nervous system. Behavioral measures are particularly important for neurotoxicity risk assessment since many known neurotoxicants do not result in neuropathology. The chlorinated hydrocarbon class consists of a wide variety of chemicals including polychlorinated biphenyls, clioquinol, trichloroethylene, hexachlorophene, organochlorine insecticides (DDT, dicofol, chlordecone, dieldrin, and lindane), and phenoxyherbicides. Each of these chemicals has effects on motor, sensory, or cognitive function that are detectable using functional measures such as behavior. Furthermore, there is evidence that if exposure occurs during critical periods of development, many of the chlorinated hydrocarbons are developmental neurotoxicants. Developmental neurotoxicity is frequently expressed as alterations in motor function or cognitive abilities or charges in the ontogeny of sensorimotor reflexes. Neurotoxicity risk assessment should include assessments of the full range of possible neurotoxicological effects, including both structural and functional indicators of neurotoxicity. 121 refs., 1 tab.

  12. The gas phase chlorination of ethane

    Energy Technology Data Exchange (ETDEWEB)

    Olsbye, Unni; Myhrvold, Elisabeth M.; Slagtern, Aase; Dahl, Ivar M. [SINTEF Applied Chemistry, Oslo (Norway)

    1999-07-01

    Light alkanes are dehydrogenated to their corresponding olefins before further reactions to more valuable chemicals. The conversion of ethane to ethene in a steam cracker requires the addition of a substantial amount of heat (90 kJ/mol). Oxidative processes for ethane dehydrogenation could in principle be carried out adiabatically, however, the oxidation selectivity towards hydrogen is too low in existing systems, which leads to low ethene selectivities. This paper discusses the potential for light alkane derivatization through chlorination.

  13. Thermal diffusion of chlorine in uranium dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Pipon, Y.; Toulhoat, N.; Moncoffre, N.; Jaffrezic, H.; Gavarini, S. [Inst. de Physique Nucleaire de Lyon (IPNL), Villeurbanne (France); Martin, P. [Commissariat a l' Energie Atomique (CEA), Centre de Cadarache, DEN/DEC/SESC/LLCC, Saint-Paul lez Durance (France); Raimbault, L. [Centre d' Informatique Geologique (CIG), Ecole des Mines, Fontainebleau (France); Scheidegger, A.M. [Lab. for Waste Management, Nuclear Energy and Safety Dept. (NES), Paul Scherrer Inst. Villigen PSI (Switzerland)

    2006-07-01

    In a nuclear reactor, isotopes such as {sup 35}Cl present as impurities in the nuclear fuel are activated by thermal neutron capture. During interim storage or geological disposal of nuclear fuel, the activation products such as {sup 36}Cl may be released from the fuel to the geo/biosphere and contribute to the ''instant release fraction'' as they are likely to migrate in defects and grain boundaries. In order to differentiate diffusion mechanisms due to ''athermal'' processes during irradiation from thermally activated diffusion, both irradiation and thermal effects must be assessed. This work concerns the measurement of the thermal diffusion coefficient of chlorine in UO{sub 2}. {sup 37}Cl was implanted at a 10{sup 13} at/cm{sup 2} fluence in depleted UO{sub 2} samples which were then annealed in the 900-1200 C temperature range and finally analyzed by secondary ion mass spectrometry (SIMS) to obtain {sup 37}Cl depth profiles. The migration process appears to be rather complex, involving mechanisms such as atomic, grain boundary, directed diffusion along preferential patterns as well as trapping into sinks before successive effusion. However, using a diffusion model based on general equation of transport, apparent diffusion coefficients could be calculated for 1000 and 1100 C and a mean activation energy of 4.3 eV is proposed. This value is one of the lowest values compared to those found in literature for other radionuclides pointing out a great ability of chlorine to migrate in UO{sub 2} at relatively low temperatures. In order to unequivocally determine the diffusion behaviour of both implanted and pristine chlorine before and after thermal annealing, the structural environment of chlorine in UO{sub 2} was examined using micro X-ray fluorescence (micro-XRF) and micro X-ray absorption spectroscopy (micro-XAS). (orig.)

  14. Hydraulic fracturing with chlorine dioxide cleanup

    Energy Technology Data Exchange (ETDEWEB)

    Williams, D.A.; Newlove, J.C.; Horton, R.L.

    1990-10-23

    This patent describes a method for fracturing a subterranean formation penetrated by a wellbore. It comprises: injecting a fracturing fluid into the formation to form a vertical fracture therein, the fracturing fluid being gelled with a polymer selected from guar, guar derivatives, acrylamide, acrylamide derivatives, cellulose, cellulose derivatives, and mixtures thereof and crosslinked with an organometallic crosslinking compound and having temperature stability above about 175{degrees} F.; packing the fracture with particulate propping agent; backflowing fluids from the formation through the propped fracture to remove a portion of the polymer; injecting at matrix rates sufficient aqueous solution of chlorine dioxide down the wellbore and into the propped fracture to penetrate at least 60 feet of the propped fracture length and contact polymer in the fracturing fluid and polymer residue in the propped fracture and on the fracture walls, the amount of the chlorine dioxide in the aqueous medium being sufficient to degrade polymer in the fracturing fluid and polymer residue; permitting the chlorine dioxide to remain in contact with the polymer in the fracturing fluid and with the polymer residue on the fracture walls and in the fracture for sufficient time to degrade the polymer thereby reducing the fracturing fluid viscosity and dissolving portions of the polymer residue; and flowing formation fluid from the formation through the propped fracture and into the wellbore to remove substantial portions of the polymer and degraded polymer from the fracture.

  15. Chlorine Monoxide in the Antarctic Spring Stratosphere.

    Science.gov (United States)

    Jaramillo-Ayerbe, Mauricio

    1988-06-01

    A series of observations of stratospheric chlorine monoxide (ClO) were carried out during the austral springs of 1986 and 1987 in McMurdo Station, Antarctica, as part of two experimental campaigns sent to investigate the seasonal decrease in ozone over the antarctic continent (the ozone "hole"). Measurements of the vertical distribution of ClO were obtained by high resolution ground-based emission spectroscopy at 278 GHz, using the Stony Brook mm-wave receiver. They show the presence of an anomalous layer of lower stratospheric ClO which is not observed at other latitudes. This anomalous layer is centered at ~20 km altitude and exhibits a pronounced diurnal variation, reaching a maximum at midday and disappearing at night. During the period of Sep. 20-24, 1987, the lower-stratospheric ClO had a maximum volume mixing ratio of 1.8_sp{+0cdot5}{ -0cdot9} ppbv. A normal ClO layer centered at ~36 km was also observed, with concentrations and diurnal behavior similar to those seen in tropical latitudes. These findings are evidence of anomalous chlorine chemistry taking place in the lower stratosphere during the antarctic spring, and indicate that increasing anthropogenic chlorine is a prime causative agent in the formation of the ozone hole.

  16. Electric plasma discharge combustion synthesis of chlorine dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Dotson, R. L.; Geren, G. W.

    1984-09-18

    A process for the production of chlorine dioxide comprises feeding an inert gas to a reaction zone and applying an electrical discharge to the inert gas to produce a high temperature plasma. Chlorine gas and oxygen gas are supplied simultaneously to the reaction zone and reacted in the plasma to produce a gaseous mixture comprised of chlorine dioxide, chlorine, oxygen and inert gas, the molar ratio of oxygen to chlorine in the reaction zone being at least about 2.5;1. The gaseous mixture is recovered from the reaction zone. Chlorine dioxide, which may be recovered as a gas or reacted to produce an alkali metal chlorite, is employed as a bleaching agent and a water treatment agent.

  17. Method of improving formation permeability using chlorine dioxide

    Energy Technology Data Exchange (ETDEWEB)

    McDougall, L.A.; Williams, D.A.

    1991-07-16

    This patent describes a method of treating a sandstone formation containing clays or silicates. It comprises injection a treating liquid into the formation comprising an aqueous solution of: from 50 to 4,200 ppm chlorine dioxide and from 1 to 85 volume percent of carbon dioxide; permitting the chlorine dioxide to react with material in the formation; and thereafter injecting into the formation an acid solution capable of dissolving the reaction products of chlorine dioxide and the clays and silicates.

  18. Treatment of algae-induced tastes and odors by chlorine, chlorine dioxide and permanganate

    OpenAIRE

    Buffin, Lisa Webster

    1992-01-01

    Chlorine (C12(sq»' chlorine dioxide (Cl02 ) and potassium permanganate (KMn04) were evaluated as oxidants for the removal of grassy and cucumber odors associated with the pure compounds, cis-3-hexenol and trans-2, cis-6-nonadienal, respectively, and for the removal of fishy odors associated with a culture of an alga, Synura petersenii. The effects of the oxidants on the pure compounds were assessed both by Flavor Profile Analysis (FPA) and gas chromatography/mass spectrometry (GC/MS). The ef...

  19. Cyclopalladated Ferrocenylimine Catalyzed Chlorination of 2-Arylbenzoxazoles%Cyclopalladated Ferrocenylimine Catalyzed Chlorination of 2-Arylbenzoxazoles

    Institute of Scientific and Technical Information of China (English)

    冷瑜婷; 杨帆; 吴养洁; 李克

    2011-01-01

    An efficient and facile protocol for palladacycle-catalyzed chlorination of 2-arylbenzoxazoles was developed. The results represent the first examples involving the palladacycle as the catalyst for such chlorination. This chlori- nation was not a ligand-directed ortho-C--H activation, but an electrophilic substitution process at the para-position of the nitrogen atom in the benzo ring of benzoxazole moiety, the regiochemistry of which had been confirmed by HMBC spectral analysis. The catalytic system could tolerate various halogen atoms, such as F, Cl and Br, affording the corresponding products in moderate to excellent yields.

  20. Imaging with polycrystalline mercuric iodide detectors using VLSI readout

    Energy Technology Data Exchange (ETDEWEB)

    Turchetta, R.; Dulinski, W.; Husson, D.; Riester, J.L.; Schieber, M.; Zuck, A.; Melekhov, L.; Saado, Y.; Hermon, H.; Nissenbaum, J

    1999-06-01

    Potentially low cost and large area polycrystalline mercuric iodide room-temperature radiation detectors, with thickness of 100-600 {mu}m have been successfully tested with dedicated low-noise, low-power mixed signal VLSI electronics which can be used for compact, imaging solutions. The detectors are fabricated by depositing HgI{sub 2} directly on an insulating substrate having electrodes in the form of microstrips and pixels with an upper continuous electrode. The deposition is made either by direct evaporation or by screen printing HgI{sub 2} mixed with glue such as Poly-Vinyl-Butiral. The properties of these first-generation detectors are quite uniform from one detector to another. Also for each single detector the response is quite uniform and no charge loss in the inter-electrode space have been detected. Because of the low cost and of the polycrystallinity, detectors can be potentially fabricated in any size and shape, using standard ceramic technology equipment, which is an attractive feature where low cost and large area applications are needed. The detectors which act as radiation counters have been tested with a beta source as well as in a high-energy beam of 100 GeV muons at CERN, connected to VLSI, low noise electronics. Charge collection efficiency and uniformity have been studied. The charge is efficiently collected even in the space between strips indicating that fill factors of 100% could be reached in imaging applications with direct detection of radiation. Single photon counting capability is reached with VLSI electronics. These results show the potential of this material for applications demanding position sensitive, radiation resistant, room-temperature operating radiation detectors, where position resolution is essential, as it can be found in some applications in high-energy physics, nuclear medicine and astrophysics.

  1. Effect of Excessive Potassium Iodide on Rat Aorta Endothelial Cells.

    Science.gov (United States)

    Zhang, Man; Zou, Xiaoyan; Lin, Xinying; Bian, Jianchao; Meng, Huicui; Liu, Dan

    2015-08-01

    The aim of the current study was to investigate the effect of excess iodine on rat aorta endothelial cells and the potential underlying mechanisms. Rat aorta endothelial cells were cultured with iodide ion (3506, 4076, 4647, 5218, 5789, 6360, 6931, and 7512 mg/L) for 48 h. Morphological changes of cells were observed with microscope after Wright-Giemsa staining and acridine orange staining. Cell proliferation was determined with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay, and cell apoptosis was assessed with flow cytometry. The activity of superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), endothelial nitric oxide synthase (eNOS), induced nitric oxide synthase (iNOS), and concentrations of malondialdehyde (MDA), glutathione (GSH), and protein carbonyl in culture medium were determined with colorimetric method. The expression of intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) was detected by enzyme linked immunosorbent assay. The results showed that excess iodine induced abnormal morphologic changes of cells, inhibited cell proliferation, and increased apoptosis rate. Iodine also reduced the activity of SOD, GSH-Px, and concentrations of GSH and increased the concentrations of MDA and protein carbonyl in a dose-dependent manner. Moreover, excess iodine decreased the activity of eNOS and increased the activity of iNOS and the expression of ICAM-1 and VCAM-1 in culture medium. Our results suggested that excess iodine exposure increased oxidative stress, caused damage of vascular endothelial cells, and altered the expression of adhesion factors and the activity of NOS. These changes may explain the mechanisms underlying excess iodine-induced vascular injury.

  2. THERAPY OF GRAVES’ DISEASE WITH SODIUM IODIDE-131

    Directory of Open Access Journals (Sweden)

    I Wayan Hartadi Noor

    2013-11-01

    Full Text Available Normal 0 false false false EN-US X-NONE X-NONE MicrosoftInternetExplorer4 Graves’ disease is the most common form of thyrotoxicosis, with a peak incidence in the 20-40 year of age group. Females are involved about five times more commonly than male. The easiest sign to recognize patients with Graves’ disease is the present of Graves’ ophthalmopathy. The diagnosis of Graves’ disease may sometimes base only on a physical examination and a medical history. Diffuse thyroid enlargement and sign of thyrotoxicosis, mainly ophthalmopathy and to lesser extent dermopathy, usually adequate for diagnosis. TSH test combined with FT4 test is usually the first laboratory test performs in these patients. The patients suffered Graves’ disease can be treated with antithyroid drug therapy or undergo subtotal Thyroidectomy. Another therapy is by using sodium iodide-131, where this therapy has advantages including easy administration, effectiveness, low expense, and absence of pain. /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0in 5.4pt 0in 5.4pt; mso-para-margin:0in; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:"Times New Roman"; mso-bidi-theme-font:minor-bidi;}

  3. Modeling the Detection of Organic and Inorganic Compounds Using Iodide-Based Chemical Ionization.

    Science.gov (United States)

    Iyer, Siddharth; Lopez-Hilfiker, Felipe; Lee, Ben H; Thornton, Joel A; Kurtén, Theo

    2016-02-04

    Iodide-based chemical ionization mass spectrometry (CIMS) has been used to detect and measure concentrations of several atmospherically relevant organic and inorganic compounds. The significant electronegativity of iodide and the strong acidity of hydroiodic acid makes electron transfer and proton abstraction essentially negligible, and the soft nature of the adduct formation ionization technique reduces the chances of sample fragmentation. In addition, iodide has a large negative mass defect, which, when combined with the high resolving power of a high resolution time-of-flight chemical ionization mass spectrometer (HR-ToF-CIMS), provides good selectivity. In this work, we use quantum chemical methods to calculate the binding energies, enthalpies and free energies for clusters of an iodide ion with a number of atmospherically relevant organic and inorganic compounds. Systematic configurational sampling of the free molecules and clusters was carried out at the B3LYP/6-31G* level, followed by subsequent calculations at the PBE/SDD and DLPNO-CCSD(T)/def2-QZVPP//PBE/aug-cc-pVTZ-PP levels. The binding energies, enthalpies, and free energies thus obtained were then compared to the iodide-based University of Washington HR-ToF-CIMS (UW-CIMS) instrument sensitivities for these molecules. We observed a reasonably linear relationship between the cluster binding enthalpies and logarithmic instrument sensitivities already at the PBE/SDD level, which indicates that relatively simple quantum chemical methods can predict the sensitivity of an iodide-based CIMS instrument toward most molecules. However, higher level calculations were needed to treat some outlier molecules, most notably oxalic acid and methylerythritol. Our calculations also corroborated the recent experimental findings that the molecules that the UW-CIMS detects at maximum sensitivity usually have binding enthalpies to iodide which are higher than about 26 kcal/mol, depending slightly on the level of theory.

  4. Iodide Residues in Milk Vary between Iodine-Based Teat Disinfectants.

    Science.gov (United States)

    French, Elizabeth A; Mukai, Motoko; Zurakowski, Michael; Rauch, Bradley; Gioia, Gloria; Hillebrandt, Joseph R; Henderson, Mark; Schukken, Ynte H; Hemling, Thomas C

    2016-07-01

    Majority of iodine found in dairy milk comes from the diet and teat disinfection products used during milking process. The objective of this study was to evaluate the effects of 4 iodine-based teat dips on milk iodide concentrations varying in iodine level (0.25% vs. 0.5%, w/w), normal low viscosity dip versus barrier dip, and application method (dip vs. spray) to ensure safe iodine levels in dairy milk when these products are used. The iodine exposure study was performed during a 2-wk period. The trial farm was purged of all iodine-based disinfection products for 21 d during a prestudy "washout period," which resulted in baseline milk iodide range of 145 to 182 ppb. During the experiment, iodine-based teat dips were used as post-milking teat disinfectants and compared to a non-iodine control disinfectant. Milk iodide residue levels for each treatment was evaluated from composited group samples. Introduction of different iodine-based teat disinfectants increased iodide residue content in milk relative to the control by between 8 and 29 μg/L when averaged across the full trial period. However, residues levels for any treatment remained well below the consumable limit of 500 μg/L. The 0.5% iodine disinfectant increased milk iodide levels by 20 μg/L more compared to the 0.25% iodine. Compared to dip-cup application, spray application significantly increased milk iodide residue by 21 μg/L and utilized approximately 23% more teat dip. This carefully controlled study demonstrated an increase in milk iodide concentrations from iodine disinfectants, but increases were small and within acceptable limits.

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

    Science.gov (United States)

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

    2014-09-01

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

  6. Effects of chlorine and chlorine dioxide on mutagenic activity of Lake Kinnereth water

    Energy Technology Data Exchange (ETDEWEB)

    Guttman-Bass, N.; Bairey-Albuquerque, M.; Ulitzur, S.; Chartrand, A.; Rav-Acha, C.

    1987-03-01

    Water from Lake Kinnereth (Israel) was tested for the presence of mutagenic activity, with and without disinfection by chlorine and chlorine dioxide. The samples were assayed for activity with two Ames Salmonella typhimurium tester strains, TA 104 and TA 100, and by a luminescent genotoxic assay with a dark mutant strain of Photobacterium fischeri. The water concentrates were mutagenic in strain TA 104 and in the luminescent assay, reaching positive mutagenic activities in the equivalent of 20 mL of water. Chlorination did not greatly affect the net mutagenic activity, although ClO/sub 2/ apparently reduced it. Humic acids were isolated from lake sediment and were assayed with and without disinfection in distilled water and in lake water from which the organic components were removed. The humic acids were mutagenic in both test systems, and treatment with Cl/sub 2/ generally decreased the net activity. ClO/sub 2/ also tended to decrease the mutagenic activity, and cytotoxic effects were observed in some of the samples. Conversely, commercial humic acid was mutagenic only after chlorination on strain TA 100. 54 references, 3 figures, 6 tables.

  7. Cellular Response of the Amoeba Acanthamoeba castellanii to Chlorine, Chlorine Dioxide, and Monochloramine Treatments ▿

    Science.gov (United States)

    Mogoa, Emerancienne; Bodet, Charles; Morel, Franck; Rodier, Marie-Hélène; Legube, Bernard; Héchard, Yann

    2011-01-01

    Acanthamoeba castellanii is a free-living amoebae commonly found in water systems. Free-living amoebae might be pathogenic but are also known to bear phagocytosis-resistant bacteria, protecting these bacteria from water treatments. The mode of action of these treatments is poorly understood, particularly on amoebae. It is important to examine the action of these treatments on amoebae in order to improve them. The cellular response to chlorine, chlorine dioxide, and monochloramine was tested on A. castellanii trophozoites. Doses of disinfectants leading to up to a 3-log reduction were compared by flow cytometry and electron microscopy. Chlorine treatment led to size reduction, permeabilization, and retraction of pseudopods. In addition, treatment with chlorine dioxide led to a vacuolization of the cytoplasm. Monochloramine had a dose-dependent effect. At the highest doses monochloramine treatment resulted in almost no changes in cell size and permeability, as shown by flow cytometry, but the cell surface became smooth and dense, as seen by electron microscopy. We show that these disinfectants globally induced size reduction, membrane permeabilization, and morphological modifications but that they have a different mode of action on A. castellanii. PMID:21602398

  8. [Determination of iodide, thiocyanate and perchlorate ions in environmental water by two-dimensional ion chromatography].

    Science.gov (United States)

    Lin, Li; Wang, Haibo; Shi, Yali

    2013-03-01

    A procedure for the determination of iodide, thiocyanate and perchlorate ions in environmental water by two-dimensional ion chromatography has been developed. At first the iodide, thiocyanate and perchlorate ions were separated from interfering ions by a column (IonPac AS16, 250 mm x 4 mm). The iodide ion, thiocyanate and perchlorate ions were then enriched with an enrichment column (MAC-200, 80 mm x 0.75 mm). In the 2nd-dimensional chromatography, iodide thiocyanate and perchlorate ions were separated and quantified by a capillary column (IonPac AS20 Capillary, 250 mm x 0.4 mm). The linear ranges were 0.05 -100 pg/L with correlation coefficients of 0. 999 9, and the detection limits were 0. 02 - 0.05 micro gg/L. The spiked recoveries of iodide, thiocyanate and perchlorate ions were in the range of 85.1% to 100.1%. The relative standard deviations of the recoveries were 1.7% to 4.9%.

  9. Trapping radiodine, in the form of methyl iodide, on nuclear carbon

    Energy Technology Data Exchange (ETDEWEB)

    Nacapricha, D. [Mahidol Univ., Bangkok (Thailand); Taylor, C. [John Moores Univ., Liverpool (United Kingdom)

    1996-12-31

    Studies have been performed on potassium-iodide-impregnated charcoals of the type used in the nuclear industry for trapping radioiodine released during nuclear fission. The effects of various parameters on the trapping efficiency of methyl iodide have been investigated. A variation in particle size within a bulk charcoal caused poor precision in K value measurements because of differences in surface area, pore volume, and bed density, leading to differences in the deposition of the impregnant. Precision is improved by sieving the charcoal to a narrower size because smaller particles have a higher porosity. This finding is supported by surface area and pore measurements. Two methods of impregnation are compared by measuring K values and the deposition of potassium iodide. Charcoal impregnated by rotary evaporation exhibits both higher K values and higher potassium iodide contents than sprayed charcoal. Two designs of spraying drum are compared: a drum with helical vanes allows more efficient deposition and more uniform distribution of impregnant than a drum with axial vanes. A decrease in the K value with increasing humidity correlates with the available surface area. A similar correlation exists between water content and available pore volume. Aging of potassium-iodide-impregnated charcoal, caused by the formation of oxygen complexes on the surface, is associated with significant falls in K value. K values of charcoals also can be restored to at least their original values by heat treatment in the absence of air. 12 refs., 6 figs., 1 tab.

  10. Estradiol decreases iodide uptake by rat thyroid follicular FRTL-5 cells

    Directory of Open Access Journals (Sweden)

    Furlanetto T.W.

    2001-01-01

    Full Text Available Estradiol has well-known indirect effects on the thyroid. A direct effect of estradiol on thyroid follicular cells, increasing cell growth and reducing the expression of the sodium-iodide symporter gene, has been recently reported. The aim of the present investigation was to study the effect of estradiol on iodide uptake by thyroid follicular cells, using FRTL-5 cells as a model. Estradiol decreased basal iodide uptake by FRTL-5 cells from control levels of 2.490 ± 0.370 to 2.085 ± 0.364 pmol I-/µg DNA at 1 ng/ml (P<0.02, to 1.970 ± 0.302 pmol I-/µg DNA at 10 ng/ml (P<0.003, and to 2.038 ± 0.389 pmol I-/µg DNA at 100 ng/ml (P<0.02. In addition, 4 ng/ml estradiol decreased iodide uptake induced by 0.02 mIU/ml thyrotropin from 8.678 ± 0.408 to 7.312 ± 0.506 pmol I-/µg DNA (P<0.02. A decrease in iodide uptake by thyroid cells caused by estradiol has not been described previously and may have a role in goiter pathogenesis.

  11. Processes of adsorption/desorption of iodides and cadmium cations onto/from Ag(111

    Directory of Open Access Journals (Sweden)

    VLADIMIR D. JOVIĆ

    2011-02-01

    Full Text Available In this work, the adsorption/desorption processes of iodides and cadmium cations in the presence of iodides onto/from Ag(111 were investigated. It was shown that both processes were complex, characterized by several peaks on the cyclic voltammograms (CVs. By PeakFit analysis of the recorded CVs and subsequent fitting of the obtained peaks by the Frumkin adsorption isotherm, the interaction parameter (f and the Gibbs energy of adsorption (DGads for each adsorbed phase were determined. In the case of iodide adsorption, four peaks were characterized by negative values of f, indicating attractive lateral interaction between the adsorbed anions, while two of them possessed value of f < –4, indicating phase transition processes. The adsorption/desorption processes of cadmium cations (underpotential deposition – UPD of cadmium in the presence of iodide anions was characterized by two main peaks, each of them being composed of two or three peaks with negative values of f. By the analysis of charge vs. potential dependences obtained either from the CVs or current transients on potentiostatic pulses, it was concluded that adsorbed iodides did not undergo desorption during the process of Cd UPD, but became replaced by Cd ad-atoms and remained adsorbed on top of a Cd layer and/or in between Cd the ad-atoms.

  12. Proton and iodine-127 nuclear magnetic resonance studies on the binding of iodide by lactoperoxidase

    Energy Technology Data Exchange (ETDEWEB)

    Sakurada, J.; Takahashi, S.; Shimizu, T.; Hatano, M.; Nakamura, S.; Hosoya, T.

    1987-10-06

    Interaction of an iodide ion with lactoperoxidase was studied by the use of /sup 1/H NMR, /sup 127/I NMR, and optical difference spectrum techniques. /sup 1/H NMR spectra demonstrated that a major broad hyperfine-shifted signal at about 60 ppm, which is ascribed to the heme peripheral methyl protons, was shifted toward high field by adding KI, indicating the binding of iodide to the active site of the enzyme; the dissociation constant was estimated to be 38 mM at pH 6.1. The binding was further detected by /sup 127/I NMR, showing no competition with cyanide. Both /sup 1/H NMR and /sup 127/I NMR revealed that the binding of iodide to the enzyme is facilitated by the protonation of an ionizable group with a pK/sup a/ value of 6.0-6.8, which is presumably the distal histidyl residue. Optical difference spectra showed that the binding of an aromatic donor molecule to the enzyme is slightly but distinctly affected by adding KI. On the basis of these results, it was suggested that an iodide ion binds to lactoperoxidase outside the heme crevice but at the position close enough to interact with the distal histidyl residue which possibly mediates electron transport in the iodide oxidation reaction.

  13. Scenarios Evaluation Tool for Chlorinated Solvent MNA

    Energy Technology Data Exchange (ETDEWEB)

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

    2007-02-28

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

  14. Advantages and disadvantages of chemical oxidation and disinfection by ozone and chlorine dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Fiessinger, F.; Richard, Y.; Montiel, A.; Musquere, P.

    1981-04-01

    Ozone and chlorine dioxide present definite advantages and disadvantages over chlorination. Chlorination, particularly for the removal of ammonia and the maintenance of a disinfectant residual in the distribution system has decisive advantages and will be difficult to replace. Ozone and chlorine dioxide seem to produce fewer carcinogenic by-products but the risk for acute toxicity, especially from the chlorites which follow chlorine dioxide, is higher than with chlorine. Chlorine dioxide and more particularly ozone should be considered as useful complements to chlorination, but no strong oxidative treatment should be applied before most of the organic matter has been removed.

  15. 78 FR 66767 - Chlorinated Isocyanurates From China and Japan

    Science.gov (United States)

    2013-11-06

    ... publishing the notice in the Federal Register of September 10, 2013 (78 FR 55293). The conference was held in... COMMISSION Chlorinated Isocyanurates From China and Japan Determinations On the basis of the record \\1... injured by reason of imports from China and Japan of chlorinated isocyanurates, provided for...

  16. Experimental and Theoretical Studies of Atmosphereic Inorganic Chlorine Chemistry

    Science.gov (United States)

    Sander, Stanley P.; Friedl, Randall R.

    1993-01-01

    Over the last five years substantial progress has been made in defining the realm of new chlorine chemistry in the polar stratosphere. Application of existing experimental techniques to potentially important chlorine-containing compounds has yielded quantitative kinetic and spectroscopic data as well as qualitative mechanistic insights into the relevant reactions.

  17. Chlorine Dioxide Induced Multiple Chemical Sensitivity: MMPI Validity Problems.

    Science.gov (United States)

    Tentoni, Stuart C.

    This paper discusses Minnesota Multiphasic Personality Inventory (MMPI) data obtained from individuals exposed to chlorine dioxide in the workplace who developed Multiple Chemical Sensitivity Syndrome. The paper explores current research on chlorine dioxide exposed persons who were misdiagnosed on the basis of MMPI interpretations. Difficulties…

  18. 75 FR 23303 - Chlorinated Isocyanurates From China and Spain

    Science.gov (United States)

    2010-05-03

    ... COMMISSION Chlorinated Isocyanurates From China and Spain AGENCY: United States International Trade... isocyanurates from China and Spain. SUMMARY: The Commission hereby gives notice that it has instituted reviews... revocation of the antidumping duty orders on chlorinated isocyanurates from China and Spain would be...

  19. 75 FR 51113 - Chlorinated Isocyanurates From China and Spain

    Science.gov (United States)

    2010-08-18

    ... COMMISSION Chlorinated Isocyanurates From China and Spain AGENCY: United States International Trade... chlorinated isocyanurates from China and Spain. SUMMARY: The Commission hereby gives notice of the scheduling... from China and Spain would be likely to lead to continuation or recurrence of material injury within...

  20. Chlorine-containing natural compounds in higher plants

    DEFF Research Database (Denmark)

    Engvild, Kjeld Christensen

    1986-01-01

    More than 130 chlorine-containing compounds have been isolated from higher plants and ferns; about half are polyacetylenes, thiophenes and sesquiterpene lactones from the Asteraceae. A chlorinated chlorophyll may be an important part of photosystem 1. High biological activity is found in 4...

  1. Quantification of propidium iodide delivery with millisecond electric pulses: A model study

    CERN Document Server

    Yu, Miao

    2014-01-01

    A model study of propidium iodide delivery with millisecond electric pulses is presented; this work is a companion of the experimental efforts by Sadik et al. [1]. Both membrane permeabilization and delivery are examined with respect to six extra-cellular conductivities. The transmembrane potential of the permeabilized regions exhibits a consistent value, which corresponds to a bifurcation point in the pore-radius-potential relation. Both the pore area density and membrane conductance increase with an increasing extra-cellular conductivity. On the other hand, the inverse correlation between propidium iodide delivery and extra-cellular conductivity as observed in the experiments is quantitatively captured by the model. This agreement confirms that this behavior is primarily mediated by electrophoretic transport during the pulse. The results suggest that electrophoresis is important even for the delivery of small molecules such as propidium iodide. The direct comparison between model prediction and experimental...

  2. Salty glycerol versus salty water surface organization: bromide and iodide surface propensities.

    Science.gov (United States)

    Huang, Zishuai; Hua, Wei; Verreault, Dominique; Allen, Heather C

    2013-07-25

    Salty NaBr and NaI glycerol solution interfaces are examined in the OH stretching region using broadband vibrational sum frequency generation (VSFG) spectroscopy. Raman and infrared (IR) spectroscopy are used to further understand the VSFG spectroscopic signature. The VSFG spectra of salty glycerol solutions reveal that bromide and iodide anions perturb the interfacial glycerol organization in a manner similar as that found in aqueous halide salt solutions, thus confirming the presence of bromide and iodide anions at the glycerol surface. Surface tension measurements are consistent with the surface propensity suggested by the VSFG data and also show that the surface excess increases with increasing salt concentration, similar to that of water. In addition, iodide is shown to have more surface prevalence than bromide, as has also been determined from aqueous solutions. These results suggest that glycerol behaves similarly to water with respect to surface activity and solvation of halide anions at its air/liquid interface.

  3. Preparation, Characterization and Optical Properties of Host-guest Nanocomposite Material Mordenite-silver Iodide

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    Silver iodide nanoclusters were successfully prepared in the channels of mordenite by a heat diffusion method. Powder X-ray diffraction, adsorption technique and infrared spectroscopy were used to characterize the prepared materials, which showed that the guest silver iodide had been encapsulated in the channels of mordenite. The optical properties of the solid phase diffuse reflectance absorption of nanocomposite material NaM-AgI were studied, showing that the absorption bands of the diffuse reflectance absorption of the prepared material moved to the region of high energy. The absorption peak of the material prepared shifted to the region of high energy. Namely, blue shift was caused. This has demonstrated the incorporation of silver iodide into the channels of the zeolite. We observed the luminescence and surface photovoltage spectra of NaM-AgI sample, proposing the mechanisms of the photoluminescence and photovoltaic responses.

  4. New Microporous Polymer Electrolyte Based on Polysiloxane Grafted with Imidazolium Iodide Moieties for DSSC

    Directory of Open Access Journals (Sweden)

    Yan Yang

    2011-01-01

    Full Text Available Two types of polysiloxane grafted with different ratio of imidazolium iodide moieties (IL-SiO2 have been synthesized to develop a micro-porous polymer electrolyte for quasi-solid-state dye-sensitized solar cells. The samples were characterized by 1HNMR, FT-IR spectrum, XRD, TEM and SEM, respectively. Moreover, the ionic conductivity of the electrolytes was measured by electrochemical workstation. Nanostructured polysiloxane containing imidazolium iodide showed excellent compatibility with organic solvent and polymer matrix for its ionic liquid characteristics. Increasing the proportion of imidazolium iodide moieties in polysiloxane improved the electrochemical behavior of the gel polymer electrolyte. A dye-sensitized solar cell with gel polymer electrolyte yielded an open-circuit voltage of 0.70 V, short-circuit current of 11.19 mA cm−2, and the conversion efficiency of 3.61% at 1 sun illumination.

  5. Optimization of mercuric iodide platelets growth by the polymer controlled vapor transport method

    Directory of Open Access Journals (Sweden)

    Fornaro L.

    1999-01-01

    Full Text Available Mercuric iodide crystals in their platelet habit were grown by the polymer controlled vapor transport method. Mercuric iodide 99% in purity was sublimated at temperatures about 122 - 126 °C and vacuum conditions (10-5 mmHg, after selecting an appropriate polymer. Temperature profiles and experimental heat transfer models were determined for two growth furnaces using different insulator configurations for the cold extreme (air, ceramic wool, grilon, copper and ceramic wool. Growth conditions for few and separate nucleation points and large crystals were determined. Representative samples were characterized by optical microscopy and by measuring the current density and apparent resistivity of the material. Future optimization and comparisons with others mercuric iodide crystal growth methods are included.

  6. Effect of Cytokine on the Expression of Sodium Iodide Symporter Gene in Breast Cancer Cell

    Institute of Scientific and Technical Information of China (English)

    JIAYue; LIUChao; TANGWei; LIUCui-ping; QINYou-wen; YUANQing-xing; LIQian; MAOXiao-dong; DIFu-song

    2004-01-01

    To investigate the effect of cytokines (TNF-α, IFN-γ and IL-6) on the expression of sodi-um-iodide symporter(NIS) gene in breast cancer cell (MCF-7). Methods:The breast cancer cell was cultureds with negative control culture or cultures with different concentrations of cytokines for 72 h. NIS germ mRNA in breast cancer cells cultured was determined by reverse transcriptase-polymerase chain reaction(RT-PCR). Results:Expression of sodium-iodide symporter mRNA can be found decreasing along with increasing the concentration of cytokine dose-depen-dently. Conchzs/on ~ Cytokine may play a role in iodide-uptake modulating in breast cancer cells by their effect on NIS germ expression.

  7. Effects of short-chain chlorinated paraffins on soil organisms.

    Science.gov (United States)

    Bezchlebová, Jitka; Cernohlávková, Jitka; Kobeticová, Klára; Lána, Jan; Sochová, Ivana; Hofman, Jakub

    2007-06-01

    Despite the fact that chlorinated paraffins have been produced in relatively large amounts, and high concentrations have been found in sewage sludge applied to soils, there is little information on their concentrations in soils and the effect on soil organisms. The aim of this study was to investigate the toxicity of chlorinated paraffins in soils. The effects of short-chain chlorinated paraffins (64% chlorine content) on invertebrates (Eisenia fetida, Folsomia candida, Enchytraeus albidus, Enchytraeus crypticus, Caenorhabditis elegans) and substrate-induced respiration of indigenous microorganisms were studied. Differences were found in the sensitivity of the tested organisms to short-chain chlorinated paraffins. F. candida was identified as the most sensitive organism with LC(50) and EC(50) values of 5733 and 1230 mg/kg, respectively. Toxicity results were compared with available studies and the predicted no effect concentration (PNEC) of 5.28 mg/kg was estimated for the soil environment, based on our data.

  8. Low-Cost Graphite-Based Free Chlorine Sensor.

    Science.gov (United States)

    Pan, Si; Deen, M Jamal; Ghosh, Raja

    2015-11-01

    Pencil lead was used to fabricate a graphite-based electrode for sensing applications. Its surface was electrochemically modified using ammonium carbamate to make it suitable for sensing free chlorine in water samples. Chlorine is widely used as a disinfectant in the water industry, and the residual free chlorine concentration in water distributed to the consumers must be lower than that stipulated by regulatory bodies. The graphite-based amperometric sensor gave a selective and linear response to free chlorine in the relevant concentration range and no response to commonly interfering ions. It was evaluated further for storage stability, response time, and hysteresis. This sensor is being proposed as a low-cost device for determining free chlorine in water samples. Its ease-of-use, limitations, and feasibility for mass-production and application is discussed.

  9. Biodegradability of Chlorinated Anilines in Waters

    Institute of Scientific and Technical Information of China (English)

    CHAO WANG; GUAN-GHUA LU; YAN-JIE ZHOU

    2007-01-01

    Objective To identify the bacteria tolerating chlorinated anilines and to study the biodegradability of o-chloroaniline and its coexistent compounds. Methods Microbial community of complex bacteria was identified by plate culture observation techniques and Gram stain method. Bacterial growth inhibition test was used to determine the tolerance of complex bacteria to toxicant. Biodegradability of chlorinated anilines was determined using domesticated complex bacteria as an inoculum by shaking-flask test. Results The complex bacteria were identified, consisting of Xanthomonas, Bacillus alcaligenes,Acinetobacter, Pseudomonas, and Actinomycetaceae nocardia. The obtained complex bacteria were more tolerant to o-chloroaniline than mixture bacteria in natural river waters. The effects of exposure concentration and inoculum size on the biodegradability of o-chloroaniline were analyzed, and the biodegradation characteristics of single o-chloroaniline and 2,4-dichloroaniline were compared with the coexistent compounds. Conclusion The biodegradation rates can be improved by decreasing concentration of compounds and increasing inoculum size of complex bacteria. When o-chloroaniline coexists with aniline, the latter is biodegraded prior to the former, and as a consequence the metabolic efficiency of o-chloroaniline is improved with the increase of aniline concentration. Meanwhile, when o-chloroaniline coexists with 2,4-dichloroaniline, the metabolic efficiency of 2,4-dichloroaniline is markedly improved.

  10. All-Solid-State Iodide Selective Electrode for Iodimetry of Iodized Salts and Vitamin C

    Directory of Open Access Journals (Sweden)

    TIRUWORK MEQUANINT

    2012-12-01

    Full Text Available A laboratory-made all-solid state iodide selective electrode, with Ag2S-AgI coated on a graphite rod recovered from dry cell battery, was prepared according to previous procedures. The electrode’s linear response to iodide was in the concentration range of 10-6 M to 10-1 M with a slope of 56.85 mV/decade and a detection limit of 6×10-7M. Iodate recovery test for laboratory formulated iodate-iodized salt was found to be 98.6 % with a standard deviation of 1.14%. The titratability of the iodized salt solution was at least 10-200 ppm potassium iodate (6-120 ppm iodine, exhibiting distinct endpoints in the range wider than the ones set in regulatory standards and reflecting that QC monitoring in production and stability decline of iodine content upon storage can be performed with the electrode method. On the basis this potentiometric titration, the application of the laboratory-made iodide electrode (vs. a saturated calomel reference electrode was extended to the determination of iodine in commercial iodized salts. In all the iodine assays, the iodate-iodized salt was initially treated with acid and an excess of iodide before titration against Na2S2O3 solution. The iodine content in table salts iodized with iodide was determined by direct potentiometry. The electrode was further used for vitamin C (ascorbic acid determinations in pharmaceutical tablets and orange juice by back titrating excess I3- against standard Na2S2O3 in acidic media. The overall outcome is that the iodide ISE can be used as sharp endpoint indicator for these titrimetric reactions in place of the well known official, but visually monitored, starch- triodide end-point reaction detection.

  11. Synergetic Inactivation of Microorganisms in Drinking Water by Short-term Free Chlorination and Subsequent Monochloramination

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    To introduce synergetic inactivation of microorganisms in drinking water by short-term free chlorination for less than 15 minutes followed by monochloramination. Methods Indicator microorganisms such as Escherichia coli,Staphylococcus aureus, Candida albicans, and spores of Bacillus subtilis were used to assess the efficiency of sequential chlorination and free chlorination. Results The sequential chlorination was more efficient in inactivating these microorganisms than free chlorination, indicating that synergy was provided by free chlorine and monochloramine. Ammonia addition time, temperature and pH had influences on this synergy. Conclusion The possible mechanism of this synergy might involve three aspects: free chlorine causing sublethal injury to microorganisms and monochloramine further inactivating them; different ability of free chlorine and monochloramine to penetrate and inactivate microorganism congeries; and higher concentration of residual chlorine in sequential chlorination than in free chlorination.

  12. Chlorine inactivation of Tubifex tubifex in drinking water and the synergistic effect of sequential inactivation with UV irradiation and chlorine.

    Science.gov (United States)

    Nie, Xiao-Bao; Li, Zhi-Hong; Long, Yuan-Nan; He, Pan-Pan; Xu, Chao

    2017-06-01

    The inactivation of Tubifex tubifex is important to prevent contamination of drinking water. Chlorine is a widely-used disinfectant and the key factor in the inactivation of T. tubifex. This study investigated the inactivation kinetics of chlorine on T. tubifex and the synergistic effect of the sequential use of chlorine and UV irradiation. The experimental results indicated that the Ct (concentration × timereaction) concept could be used to evaluate the inactivation kinetics of T. tubifex with chlorine, thus allowing for the use of a simpler Ct approach for the assessment of T. tubifex chlorine inactivation requirements. The inactivation kinetics of T. tubifex by chlorine was found to be well-fitted to a delayed pseudo first-order Chick-Watson expression. Sequential experiments revealed that UV irradiation and chlorine worked synergistically to effectively inactivate T. tubifex as a result of the decreased activation energy, Ea, induced by primary UV irradiation. Furthermore, the inactivation effectiveness of T. tubifex by chlorine was found to be affected by several drinking water quality parameters including pH, turbidity, and chemical oxygen demand with potassium permanganate (CODMn) concentration. High pH exhibited pronounced inactivation effectiveness and the decrease in turbidity and CODMn concentrations contributed to the inactivation of T. tubifex.

  13. Change in genotoxicity of wastewater during chlorine dioxide and chlorine disinfections and the influence of ammonia nitrogen

    Institute of Scientific and Technical Information of China (English)

    WANG Lisha; HU Hongying; WANG Chao; Koichi Fujie

    2007-01-01

    The effects of chlorine dioxide and chlorine disinfections on the genotoxicity of different biologically treated sewage wastewater samples were studied by umu-test.The experiment results showed that when chlorine dioxide dosage was increased from 0 to 30 mg/L,the genotoxicity of wastewater first decreased rapidly and then tended to be stable,while when the chlorine dosage was increased from 0 to 30 mg/L,the genotoxicity of wastewater changed diversely for different samples.It was then found that ammonia nitrogen did not affect the change of genotoxicity during chlorine dioxide disinfection of wastewater,while it greatly affected the change of genotoxicity during chlorine disinfection of wastewater.When the concentration of ammonia nitrogen was low(<10-20mg/L),the genotoxicity of wastewater decreased after chlorine disinfection,and when the concentration of ammonia nitrogen was high(>10-20 mg/L),the genotoxicity of wastewater increased after chlorine disinfection.

  14. Iodide uptake in human anaplastic thyroid carcinoma cells after transfer of the human thyroid peroxidase gene

    Energy Technology Data Exchange (ETDEWEB)

    Haberkom, U. [Clinical Cooperation Unit Nuclear Medicine, German Cancer Research Center, Heidelberg (Germany); Dept. of Nuclear Medicine, Univ. of Heidelberg (Germany); Altmann, A.; Jiang, S.; Morr, I.; Mahmut, M. [Clinical Cooperation Unit Nuclear Medicine, German Cancer Research Center, Heidelberg (Germany); Eisenhut, M. [Dept. of Nuclear Medicine, Univ. of Heidelberg (Germany)

    2001-05-01

    Human thyroperoxidase (hTPO) is critical for the accumulation of iodide in thyroid tissues. Poorly differentiated and anaplastic thyroid tumours which lack thyroid-specific gene expression fail to accumulate iodide and, therefore, do not respond to iodine-131 therapy. We consequently investigated whether transfer of the hTPO gene is sufficient to restore the iodide-trapping capacity in undifferentiated thyroid and non-thyroid tumour cells. The human anaplastic thyroid carcinoma cell lines C643 and SW1736, the rat Morris hepatoma cell line MH3924A and the rat papillary thyroid carcinoma cell line L2 were used as in vitro model systems. Employing a bicistronic retroviral vector based on the myeloproliferative sarcoma virus for the transfer of the hTPO and the neomycin resistance gene, the C643 cells and SW1736 cells were transfected while the L2 cells and MH3924A cells were infected with retroviral particles. Seven recombinant C643 and seven SW1736 cell lines as well as four recombinant L2 and four MH3924A cell lines were established by neomycin selection. They were studied for hTPO expression using an antibody-based luminescence kit, followed by determination of the enzyme activity in the guaiacol assay and of the iodide uptake capacity in the presence of Na{sup 125}I. Genetically modified cell lines expressed up to 1,800 times more hTPO as compared to wild type tumour cells. The level of hTPO expression varied significantly between individual neomycin-resistant cell lines, suggesting that the recombinant retroviral DNA was integrated at different sites of the cellular genome. The accumulation of iodide, however, was not significantly enhanced in individual recombinant cell lines, irrespective of low or high hTPO expression. Moreover, there was no correlation between hTPO expression and enzyme activity in individual cell lines. The transduction of the hTPO gene per se is not sufficient to restore iodide trapping in non-iodide-concentrating tumour cells. Future

  15. Development of W/O Microemulsion for Transdermal Delivery of Iodide Ions

    OpenAIRE

    Lou, Hao; Qiu, Ni; Crill, Catherine; Helms, Richard; Almoazen, Hassan

    2012-01-01

    The objective of this study was to develop a water-in-oil (w/o) microemulsion which can be utilized as a transdermal delivery for iodide ions. Several w/o microemulsion formulations were prepared utilizing Span 20, ethanol, Capryol 90®, and water. The selected formulations had 5%, 10%, 15%, 20%, and a maximum of 23% w/w water content. Potassium iodide (KI) was incorporated in all formulations at 5% w/v. Physicochemical characterizations were conducted to evaluate the structure and stability. ...

  16. All-Solid-State Iodide Selective Electrode for Iodimetry of Iodized Salts and Vitamin C

    OpenAIRE

    TIRUWORK MEQUANINT; GHIRMA MOGES; MERID TESSMA; SOLOMON MEHRETU

    2012-01-01

    A laboratory-made all-solid state iodide selective electrode, with Ag2S-AgI coated on a graphite rod recovered from dry cell battery, was prepared according to previous procedures. The electrode’s linear response to iodide was in the concentration range of 10-6 M to 10-1 M with a slope of 56.85 mV/decade and a detection limit of 6×10-7M. Iodate recovery test for laboratory formulated iodate-iodized salt was found to be 98.6 % with a standard deviation of 1.14%. The titratability of the iodize...

  17. Tris(1,2-dimethoxyethane-κ2O,O′iodidocalcium iodide

    Directory of Open Access Journals (Sweden)

    Siou-Wei Ou

    2012-02-01

    Full Text Available In the title complex, [CaI(C4H10O23]I, the CaII atom is seven-coordinated by six O atoms from three 1,2-dimethoxyethane (DME ligands and one iodide anion in a distorted pentagonal–bipyramidal geometry. The I atom and one of the O atoms from a DME ligand lie in the axial positions while the other O atoms lie in the basal plane. The other iodide anion is outside the complex cation.

  18. Glycosylation of Sodium/Iodide Symporter (NIS) Regulates Its Membrane Translocation and Radioiodine Uptake

    OpenAIRE

    Taemoon Chung; Hyewon Youn; Chan Joo Yeom; Keon Wook Kang; June-Key Chung

    2015-01-01

    Purpose Human sodium/iodide symporter (hNIS) protein is a membrane glycoprotein that transports iodide ions into thyroid cells. The function of this membrane protein is closely regulated by post-translational glycosylation. In this study, we measured glycosylation-mediated changes in subcellular location of hNIS and its function of iodine uptake. Methods HeLa cells were stably transfected with hNIS/tdTomato fusion gene in order to monitor the expression of hNIS. Cellular localization of hNIS ...

  19. Studying Equilibrium in the Chemical Reaction between Ferric and Iodide Ions in Solution Using a Simple and Inexpensive Approach

    Science.gov (United States)

    Nikolaychuk, Pavel Anatolyevich; Kuvaeva, Alyona Olegovna

    2016-01-01

    A laboratory experiment on the study of the chemical equilibrium based on the reaction between ferric and iodide ions in solution with the formation of ferrous ions, free iodine, and triiodide ions is developed. The total concentration of iodide and triiodide ions in the reaction mixture during the reaction is determined by the argentometric…

  20. Efficiency enhancement in dye sensitized solar cells using gel polymer electrolytes based on a tetrahexylammonium iodide and MgI2 binary iodide system.

    Science.gov (United States)

    Bandara, T M W J; Dissanayake, M A K L; Jayasundara, W J M J S R; Albinsson, I; Mellander, B-E

    2012-06-28

    Quasi-solid-state dye-sensitized solar cells have drawn the attention of scientists and technologists as a potential candidate to supplement future energy needs. The conduction of iodide ions in quasi-solid-state polymer electrolytes and the performance of dye sensitized solar cells containing such electrolytes can be enhanced by incorporating iodides having appropriate cations. Gel-type electrolytes, based on PAN host polymers and mixture of salts tetrahexylammonium iodide (Hex4N(+)I(-)) and MgI2, were prepared by incorporating ethylene carbonate and propylene carbonate as plasticizers. The salt composition in the binary mixture was varied in order to optimize the performance of solar cells. The electrolyte containing 120% Hex4N(+)I(-) with respect to weight of PAN and without MgI2 showed the highest conductivity out of the compositions studied, 2.5 × 10(-3) S cm(-1) at 25 °C, and a glass transition at -102.4 °C. However, the electrolyte containing 100% Hex4N(+)I(-) and 20% MgI2 showed the best solar cell performance highlighting the influence of the cation on the performance of the cell. The predominantly ionic behaviour of the electrolytes was established from the dc polarization data and all the electrolytes exhibit iodide ion transport. Seven different solar cells were fabricated employing different electrolyte compositions. The best cell using the electrolyte with 100% Hex4N(+)I(-) and 20% MgI2 with respect to PAN weight showed 3.5% energy conversion efficiency and 8.6 mA cm(-2) short circuit current density.

  1. Ultrafast measurements of chlorine dioxide photochemistry

    Energy Technology Data Exchange (ETDEWEB)

    Ludowise, P.D.

    1997-08-01

    Time-resolved mass spectrometry and time-resolved photoelectron spectroscopy are used to study the ultrafast photodissociation dynamics of chlorine dioxide, an important constituent in stratospheric ozone depletion. Chapter 1 introduces these pump/probe techniques, in which a femtosecond pump pulse excites a molecule to a dissociative state. At a later time, a second femtosecond probe pulse ionizes the molecule. The resulting mass and photoelectron spectra are acquired as a function of the delay between the pump and probe pulses, which follows the evolution of the molecule on the excited state. A comparison to other techniques used to study reaction dynamics is discussed. Chapter 2 includes a detailed description of the design and construction of the experimental apparatus, which consists of a femtosecond laser system, a molecular beam time-of-flight spectrometer, and a data acquisition system. The time-of-flight spectrometer is specifically designed to have a short flight distance to maximize the photoelectron collection efficiency without degrading the resolution, which is limited by the bandwidth of the femtosecond laser system. Typical performance of the apparatus is demonstrated in a study of the time-resolved photoelectron spectroscopy of nitric oxide. The results of the time-resolved mass spectrometry experiments of chlorine dioxide are presented in Chapter 3. Upon excitation to the A {sup 2}A{sub 2} state near 3.2 eV, the molecule dissociates through an indirect two-step mechanism. The direct dissociation channel has been predicted to be open, but is not observed. A quantum beat is observed in the OClO{sup +} species, which is described as a vibrational coherence of the optically prepared A {sup 2}A{sub 2} state. Chapter 4 presents the results of the time-resolved photoelectron experiments of chlorine dioxide. At short delay time, the quantum beat of the OClO{sup +} species is observed in the X {sup 1}A{sub 1} state of the ion. At infinite delay, the signal

  2. Degradation of DEET and Caffeine under UV/Chlorine and Simulated Sunlight/Chlorine Conditions.

    Science.gov (United States)

    Sun, Peizhe; Lee, Wan-Ning; Zhang, Ruochun; Huang, Ching-Hua

    2016-12-20

    Photoactivation of aqueous chlorine could promote degradation of chlorine-resistant and photochemically stable chemicals accumulated in swimming pools. This study investigated the degradation of two such chemicals, N,N-diethyl-3-methylbenzamide (DEET) and caffeine, by low pressure ultraviolet (UV) light and simulated sunlight (SS) activated free chlorine (FC) in different water matrices. Both DEET and caffeine were rapidly degraded by UV/FC and SS/FC but exhibited different kinetic behaviors. The degradation of DEET followed pseudo-first-order kinetics, whereas the degradation of caffeine accelerated with reaction. Mechanistic study revealed that, under UV/FC, ·OH and Cl· were responsible for degradation of DEET, whereas ClO· related reactive species (ClOrrs), generated by the reaction between FC and ·OH/Cl·, played a major role in addition to ·OH and Cl· in degrading caffeine. Reaction rate constants of DEET and caffeine with the respective radical species were estimated. The imidazole moiety of caffeine was critical for the special reactivity with ClOrrs. Water matrix such as pH had a stronger impact on the UV/FC process than the SS/FC process. In saltwater matrix under UV/FC and SS/FC, the degradation of DEET was significantly inhibited, but the degradation of caffeine was much faster than that in nonsalty solutions. The interaction between Br(-) and Cl(-) may play an important role in the degradation of caffeine by UV/FC in saltwater. Reaction product analysis showed similar product patterns by UV/FC and SS/FC and minimal formation of chlorinated intermediates and disinfection byproducts.

  3. Does Chlorination of Seawater Reverse Osmosis Membranes Control Biofouling?

    KAUST Repository

    Khan, Muhammad Tariq

    2015-04-01

    Biofouling is the major problem of reverse osmosis (RO) membranes used for desalting seawater (SW). The use of chlorine is a conventional and common practice to control/prevent biofouling. Unlike polyamide RO membranes, cellulose triacetate (CTA) RO membranes display a high chlorine tolerance. Due to this characteristic, CTA membranes are used in most of the RO plants located in the Middle East region where the elevated seawater temperature and water quality promote the risk of membrane biofouling. However, there is no detailed study on the investigation/characterization of CTA-RO membrane fouling. In this investigation, the fouling profile of a full–scale SWRO desalination plant operating with not only continuous chlorination of raw seawater but also intermittent chlorination of CTA-RO membranes was studied. Detailed water quality and membrane fouling analyses were conducted. Profiles of microbiological, inorganic, and organic constituents of analysed fouling layers were extensively discussed. Our results clearly identified biofilm development on these membranes. The incapability of chlorination on preventing biofilm formation on SWRO membranes could be assigned to its failure in effectively reaching throughout the different regions of the permeators. This failure could have occurred due to three main factors: plugging of membrane fibers, chlorine consumption by organics accumulated on the front side fibers, or chlorine adaptation of certain bacterial populations.

  4. Chlorine diffusion in uranium dioxide under heavy ion irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Pipon, Y. [Universite Claude Bernard Lyon-1/Institut de Physique Nucleaire de Lyon (IPNL), 4, rue Enrico Fermi, 69622 Villeurbanne cedex (France) and Universite Claude Bernard Lyon-1, Institut Universitaire de Technologie (IUT A), 94, boulevard Niels Bohr, 69622 Villeurbanne cedex (France)]. E-mail: pipon@ipnl.in2p3.fr; Bererd, N. [Universite Claude Bernard Lyon-1/Institut de Physique Nucleaire de Lyon (IPNL), 4, rue Enrico Fermi, 69622 Villeurbanne cedex (France); Universite Claude Bernard Lyon-1, Institut Universitaire de Technologie (IUT A), 94, boulevard Niels Bohr, 69622 Villeurbanne cedex (France); Moncoffre, N. [Universite Claude Bernard Lyon-1/Institut de Physique Nucleaire de Lyon (IPNL), 4, rue Enrico Fermi, 69622 Villeurbanne cedex (France); Peaucelle, C. [Universite Claude Bernard Lyon-1/Institut de Physique Nucleaire de Lyon (IPNL), 4, rue Enrico Fermi, 69622 Villeurbanne cedex (France); Toulhoat, N. [Universite Claude Bernard Lyon-1/Institut de Physique Nucleaire de Lyon (IPNL), 4, rue Enrico Fermi, 69622 Villeurbanne cedex (France); Commissariat a l' Energie Atomique (CEA), DEN/Saclay, 91191 Gif sur Yvette cedex (France); Jaffrezic, H. [Universite Claude Bernard Lyon-1/Institut de Physique Nucleaire de Lyon (IPNL), 4, rue Enrico Fermi, 69622 Villeurbanne cedex (France); Raimbault, L. [Ecole des Mines de Paris, Centre de Geosciences, 35 rue Saint Honore, F-77305 Fontainebleau cedex (France); Sainsot, P. [Institut National des Sciences Appliquees de Lyon (INSA), UMR 5514, F-69621 Villeurbanne cedex (France); Carlot, G. [Commissariat a l' Energie Atomique (CEA), Centre de Cadarache, DEN/DEC/SESC/LLCC, 13108 Saint-Paul lez Durance (France)

    2007-04-15

    The radiation enhanced diffusion of chlorine in UO{sub 2} during heavy ion irradiation is studied. In order to simulate the behaviour of {sup 36}Cl, present as an impurity in UO{sub 2}, {sup 37}Cl has been implanted into the samples (projected range 200 nm). The samples were then irradiated with 63.5 MeV {sup 127}I at two fluxes and two temperatures and the chlorine distribution was analyzed by SIMS. The results show that, during irradiation, the diffusion of the implanted chlorine is enhanced and slightly athermal with respect to pure thermal diffusion. A chlorine gain of 10% accumulating near the surface has been observed at 510 K. This corresponds to the displacement of pristine chlorine from a region of maximum defect concentration. This behaviour and the mean value of the apparent diffusion coefficient found for the implanted chlorine, around 2.5 x 10{sup -14} cm{sup 2} s{sup -1}, reflect the high mobility of chlorine in UO{sub 2} during irradiation with fission products.

  5. Chlorine diffusion in uranium dioxide under heavy ion irradiation

    Science.gov (United States)

    Pipon, Y.; Bérerd, N.; Moncoffre, N.; Peaucelle, C.; Toulhoat, N.; Jaffrézic, H.; Raimbault, L.; Sainsot, P.; Carlot, G.

    2007-04-01

    The radiation enhanced diffusion of chlorine in UO2 during heavy ion irradiation is studied. In order to simulate the behaviour of 36Cl, present as an impurity in UO2, 37Cl has been implanted into the samples (projected range 200 nm). The samples were then irradiated with 63.5 MeV 127I at two fluxes and two temperatures and the chlorine distribution was analyzed by SIMS. The results show that, during irradiation, the diffusion of the implanted chlorine is enhanced and slightly athermal with respect to pure thermal diffusion. A chlorine gain of 10% accumulating near the surface has been observed at 510 K. This corresponds to the displacement of pristine chlorine from a region of maximum defect concentration. This behaviour and the mean value of the apparent diffusion coefficient found for the implanted chlorine, around 2.5 × 10-14 cm2 s-1, reflect the high mobility of chlorine in UO2 during irradiation with fission products.

  6. Does chlorination of seawater reverse osmosis membranes control biofouling?

    Science.gov (United States)

    Khan, Muhammad Tariq; Hong, Pei-Ying; Nada, Nabil; Croue, Jean Philippe

    2015-07-01

    Biofouling is the major problem of reverse osmosis (RO) membranes used for desalting seawater (SW). The use of chlorine is a conventional and common practice to control/prevent biofouling. Unlike polyamide RO membranes, cellulose triacetate (CTA) RO membranes display a high chlorine tolerance. Due to this characteristic, CTA membranes are used in most of the RO plants located in the Middle East region where the elevated seawater temperature and water quality promote the risk of membrane biofouling. However, there is no detailed study on the investigation/characterization of CTA-RO membrane fouling. In this investigation, the fouling profile of a full-scale SWRO desalination plant operating with not only continuous chlorination of raw seawater but also intermittent chlorination of CTA-RO membranes was studied. Detailed water quality and membrane fouling analyses were conducted. Profiles of microbiological, inorganic, and organic constituents of analysed fouling layers were extensively discussed. Our results clearly identified biofilm development on these membranes. The incapability of chlorination on preventing biofilm formation on SWRO membranes could be assigned to its failure in effectively reaching throughout the different regions of the permeators. This failure could have occurred due to three main factors: plugging of membrane fibers, chlorine consumption by organics accumulated on the front side fibers, or chlorine adaptation of certain bacterial populations.

  7. Removal effect on Mesocyclops leukarti and mutagenicity with chlorine dioxide

    Institute of Scientific and Technical Information of China (English)

    ZUO Jin-long; CUI Fu-yi; QU Bo; ZHU Gui-bing

    2006-01-01

    Mesocyclops leukarti of zooplankton propagates excessively in eutrophic water body and it cannot be effectively inactivated by the conventional drinking water treatment process. In order to tackle this problem, a study of removal effect on Mesocyclops leukarti with chlorine dioxide in a waterworks was performed. The results showed that Mesocyclops leukarti could be effectively removed from water by 1.0 mg/L chlorine dioxide preoxidation combined with the conventional drinking water treatment process.Higher oxidizability and molecular state of chlorine dioxide in water is the key to the inactivation of Mesocyclops leukarti. The chlorite, disinfection by-products (DBPs) of chlorine dioxide, was stable at 0.45 mg/L, which is lower than that critical value of the USEPA. GC-MS examination showed that the quantity of organic substance in the water treated by chlorine dioxide obviously decreased. Ames test further revealed that the mutagenicity was reduced by chlorine dioxide with respect to prechlorine. The propagation ofMesocyclops leukarti can be inactivated effectively and safely by chlorine dioxide pre-oxidation.

  8. Roles of reactive chlorine species in trimethoprim degradation in the UV/chlorine process: Kinetics and transformation pathways.

    Science.gov (United States)

    Wu, Zihao; Fang, Jingyun; Xiang, Yingying; Shang, Chii; Li, Xuchun; Meng, Fangang; Yang, Xin

    2016-11-01

    The UV/chlorine process, which forms several reactive species including hydroxyl radicals (HO) and reactive chlorine species (RCS) to degrade contaminants, is being considered to be an advanced oxidation process. This study investigated the kinetics and mechanism of the degradation of trimethoprim (TMP) by the UV/chlorine process. The degradation of TMP was much faster by UV/chlorine compared to UV/H2O2. The degradation followed pseudo first-order kinetics, and the rate constant (k') increased linearly as the chlorine dosage increased from 20 μM to 200 μM and decreased as pH rose from 6.1 to 8.8. k' was not affected by chloride and bicarbonate but decreased by 50% in the presence of 1-mg/L NOM. The contribution of RCS, including Cl, Cl2(-) and ClO, to the degradation removal rate was much higher than that of HO and increased from 67% to 87% with increasing pH from 6.1 to 8.8 under the experimental condition. The increasing contribution of RCS to the degradation with increasing pH was attributable to the increase in the ClO concentration. Kinetic modeling and radical scavenging tests verified that ClO mainly attacked the trimethoxybenzyl moiety of TMP. RCS reacted with TMP much faster than HOCl/OCl(-) to form chlorinated products (i.e., m/z 325) and chlorinated disinfection byproducts such as chloroform, chloral hydrate, dichloroacetonitrile and trichloronitromethane. The hydroxylation and demethylation of m/z 325 driven by HO generated m/z 327 and m/z 341. Meanwhile, reactions of m/z 325 with HO and RCS/HOCl/OCl(-) generated dichlorinated and hydroxylated products (i.e., m/z 377). All the chlorinated products could be further depleted to produce products with less degree of halogenation in the UV/chlorine process, compared to dark chlorination. The acute toxicity to Vibrio fischeri by UV/chlorine was lower than chlorination at the same removal rate of TMP. This study demonstrated the importance of RCS, in particular, ClO, in the degradation of micropollutants

  9. Simulating stable carbon and chlorine isotope ratios in dissolved chlorinated groundwater pollutants with BIOCHLOR-ISO

    Science.gov (United States)

    Höhener, Patrick

    2016-12-01

    BIOCHLOR is a well-known simple tool for evaluating the transport of dissolved chlorinated solvents in groundwater, ideal for rapid screening and teaching. This work extends the BIOCHLOR model for the calculation of stable isotope ratios of carbon and chlorine isotopes in chloroethenes. An exact solution for the three-dimensional reactive transport of a chain of degrading compounds including sorption is provided in a spreadsheet and applied for modeling the transport of individual isotopes 12C, 13C, 35Cl, 37Cl from a constant source. The model can consider secondary isotope effects that can occur in the breaking of Csbnd Cl bonds. The model is correctly reproducing results for δ13C and δ37Cl modeled by a previously published 1-D numerical model without secondary isotope effects, and is also reproducing results from a microcosm experiment with secondary chlorine isotope effects. Two applications of the model using field data from literature are further given and discussed. The new BIOCHLOR-ISO model is distributed as a spreadsheet (MS EXCEL) along with this publication.

  10. Characterization of Chlorinated Ethene Degradation in a Vertical Flow Constructed Wetland

    Science.gov (United States)

    2007-03-01

    pathway for chlorinated volatiles in phytoremediation applications. Although transpiration of chlorinated solvents has been confirmed in studies ... case study publications and conference presentations providing support for the use of constructed wetlands for the treatment of chlorinated solvent...groundwater. This study characterized and evaluated the concentration of chlorinated ethenes within a vertical flow constructed wetland, fed with PCE

  11. Safety of water treatment by chlorine dioxide oxidation of aromatic hydrocarbons commonly found in water

    Energy Technology Data Exchange (ETDEWEB)

    Taymaz, K.; Williams, D.T.; Benoit, F.M.

    1979-01-01

    The safety of water treatment by chlorine dioxide oxidation of aromatic hydrocarbons commonly found in water and industrial wastewaters in the US was studied by observing the reactions of naphthalene and methylnaphthalenes in essentially chlorine-free, aqueous chlorine dioxide solutions. Naphthalene and methylnaphthalenes yielded chlorinated derivatives and oxidation products. Further research is recommended.

  12. Behavior and stability of adenosine triphosphate (ATP) during chlorine disinfection.

    Science.gov (United States)

    Nescerecka, Alina; Juhna, Talis; Hammes, Frederik

    2016-09-15

    Adenosine triphosphate (ATP) analysis is a cultivation-independent alternative method for the determination of bacterial viability in both chlorinated and non-chlorinated water. Here we investigated the behavior and stability of ATP during chlorination in detail. Different sodium hypochlorite doses (0-22.4 mg-Cl2 L(-1); 5 min exposure) were applied to an Escherichia coli pure culture suspended in filtered river water. We observed decreasing intracellular ATP with increasing chlorine concentrations, but extracellular ATP concentrations only increased when the chlorine dose exceeded 0.35 mg L(-1). The release of ATP from chlorine-damaged bacteria coincided with severe membrane damage detected with flow cytometry (FCM). The stability of extracellular ATP was subsequently studied in different water matrixes, and we found that extracellular ATP was stable in sterile deionized water and also in chlorinated water until extremely high chlorine doses (≤11.2 mg-Cl2 L(-1); 5 min exposure). In contrast, ATP decreased relatively slowly (k = 0.145 h(-1)) in 0.1 μm filtered river water, presumably due to degradation by either extracellular enzymes or the fraction of bacteria that were able to pass through the filter. Extracellular ATP decreased considerably faster (k = 0.368 h(-1)) during batch growth of a river water bacterial community. A series of growth potential tests showed that extracellular ATP molecules were utilized as a phosphorus source during bacteria proliferation. From the combined data we conclude that ATP released from bacteria at high chlorine doses could promote bacteria regrowth, contributing to biological instability in drinking water distribution systems.

  13. Aqueous reactions of chlorine dioxide with hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Rav-Acha, C.; Choshen, E.

    1987-11-01

    In contrast to mechanisms proposed earlier in the literature, according to which chlorine dioxide (ClO/sub 2/) reacts with various hydrocarbons in aqueous media by abstracting allylic or benzylic hydrogens, it is shown that ClO/sub 2/ reacts with olefins through initial electron transfer. Hydrocarbons that can undergo facile oxidation, such as polycyclic aromatic hydrocarbons (PAH) and some olefins, react with ClO/sub 2/ quite rapidly, while saturated aliphatic hydrocarbons, some aromatic hydrocarbons, and olefins substituted with electron-withdrawing groups remain unreactive. This was substantiated by comparing the reactivities toward ClO/sub 2/ of a variety of hydrocarbons, including aliphatic and aromatic hydrocarbons, saturated and unsaturated acids, PAH, or cyclic and acyclic olefins. The results were supported by a detailed kinetic and product study of the reaction between ClO/sub 2/ and some model compounds.

  14. Iodide-induced thyrotoxicosis in a thyroidectomized patient with metastatic thyroid carcinoma

    Energy Technology Data Exchange (ETDEWEB)

    Yoshinari, M.; Tokuyama, T.; Okamura, K.; Sato, K.; Kusuda, K.; Fujishima, M.

    1988-04-15

    An unusual case of iodide-induced thyrotoxicosis is documented in this article. The patient was a 64-year-old euthyroid man with acromegaly. He also had multiple follicular and papillary thyroid carcinomas with a metastatic lesion in the lumbar vertebrae. After a total thyroidectomy, he became slightly hypothyroid, and the lumbar lesion began to incorporate /sup 131/I by scintigraphy. When an iodine-containing contrast medium happened to be injected, a transient increase of serum thyroid hormone level was observed. After complete thyroid ablation with 83 mCi of /sup 131/I, the oral administration of 100 mg of potassium iodide for 7 days induced a prominent increase of serum thyroid hormone level. These findings indicated that the metastatic thyroid carcinoma could produce excess thyroid hormone insofar as a sufficient amount of iodide was given. Although this is the first report of such a case, iodide-induced thyrotoxicosis may not be rare in patients with thyroid carcinomas because the Wolff-Chaikoff effect is thought to be lost, and the organic iodinating activity and lysosomal protease activity are well-preserved.

  15. Leaching of iodide (I(-)) and iodate (IO3(-)) anions from synthetic layered double hydroxide materials.

    Science.gov (United States)

    Theiss, Frederick L; Ayoko, Godwin A; Frost, Ray L

    2016-09-15

    Several studies have previously demonstrated that layered double hydroxides (LDHs) show considerable potential for the adsorption of radioiodine from aqueous solution; however, few studies have demonstrated that these materials are able to store radioactive (131)I for an acceptable period. The leaching of iodide (I(-)) and iodate (IO3(-)) form Mg/Al LDHs has been carried out. Contact time appeared to be a more significant variable for the leaching of iodate (IO3(-)) compared to that of iodide (I(-)). Experimental results are fitted to the pseudo second order model, suggesting that diffusion is likely to be the rate-limiting step. The presence of carbonate in the leaching solution appeared to significantly increase the leaching of iodide (I(-)) as did the presence of chloride to a lesser extent. The maximum amount of iodate (IO3(-)) leached using ultrapure water as the leaching solution was 21% of the iodate (IO3(-)) originally present. The corresponding result for iodide (I(-)) was even lower at 3%.

  16. Photodissociation of sodium iodide and resonant ionization of sodium atom produced

    Institute of Scientific and Technical Information of China (English)

    HUO Bing-hai; Z.T.Salim; A.H.Bakery

    2004-01-01

    Resonant ionization spectroscopy (RIS) and resonant ionization mass spectroscopy (RIMS) are employed to detect the photodissociation product of sodium iodide molecules in a molecular beam in an intense laser field in the absence of the buffer gases. Time of flight mass spectra is recorded. In particular, the appearances of multiphoton ionization are discussed.

  17. Preparation and Luminescence Thermochromism of Tetranuclear Copper(I)-Pyridine-Iodide Clusters

    Science.gov (United States)

    Parmeggiani, Fabio; Sacchetti, Alessandro

    2012-01-01

    A simple and straightforward synthesis of a tetranuclear copper(I)-pyridine-iodide cluster is described as a laboratory experiment for advanced inorganic chemistry undergraduate students. The product is used to demonstrate the fascinating and visually impressive phenomenon of luminescence thermochromism: exposed to long-wave UV light, the…

  18. The sodium iodide symporter (NIS) and potential regulators in normal, benign and malignant human breast tissue.

    LENUS (Irish Health Repository)

    Ryan, James

    2011-01-01

    The presence, relevance and regulation of the Sodium Iodide Symporter (NIS) in human mammary tissue remains poorly understood. This study aimed to quantify relative expression of NIS and putative regulators in human breast tissue, with relationships observed further investigated in vitro.

  19. Research data supporting "Photon recycling in lead-iodide perovskite solar cells"

    OpenAIRE

    Pazos-Outón, Luis M.; Szumilo, Monika; Lamboll, Robin; Richter, Johannes M.; Crespo-Quesada, Micaela; Abdi - Jalebi, Mojtaba; Beeson, Harry J.; Vrucinic, Milan; Alsari, Mejd; Snaith, Henry J.; Ehrler, Bruno; Friend, Richard H.; Deschler, Felix

    2016-01-01

    Data for the figures presented in the manuscript. These research data support “Photon recycling in lead-iodide perovskite solar cells” published in “Science” (http://dx.doi.org./10.1126/science.aaf1168) This work was supported by the EPSRC [grant number EP/M005143/1] and Winton Programme for the Physics of Sustainability.

  20. Real-Time Observation of Organic Cation Reorientation in Methylammonium Lead Iodide Perovskites

    NARCIS (Netherlands)

    Bakulin, Artem A.; Selig, Oleg; Bakker, Huib J.; Rezus, Yves L. A.; Mueller, Christian; Glaser, Tobias; Lovrincic, Robert; Sun, Zhenhua; Chen, Zhuoying; Walsh, Aron; Frost, Jarvist M.; Jansen, Thomas L. C.

    2015-01-01

    The introduction of a mobile and polarized organic moiety as a cation in 3D lead-iodide perovskites brings fascinating optoelectronic properties to these materials. The extent and the time scales of the orientational mobility of the organic cation and the molecular mechanism behind its motion remain

  1. Multiple subcutaneous mycetomas caused by Pseudallescheria boydii: response to therapy with oral potassium iodide solution.

    Science.gov (United States)

    Khan, Fida A; Hashmi, Shahrukh; Sarwari, Arif R

    2010-02-01

    We describe the case of a sixteen-year-old male who presented with multiple subcutaneous mycetomas proven on culture to be secondary to Pseudallescheria boydi., The lesions responded completely to oral potassium iodide solution. To our knowledge this has never been reported in humans.

  2. Regioselective iodination of aromatic compounds with potassium iodide in the presence of benzyltriphenylphosphonium perchlorate

    Institute of Scientific and Technical Information of China (English)

    Jalal Albadi; Masoumeh Abedini; Nasir Iravani

    2012-01-01

    A simple and efficient method for the selective iodination of various aromatic compounds by using potassium iodide in the presence of benzyltriphenylphosphonium perchlorate,is reported.This method provides several advantages such as good selectivity between ortho and para positions of aromatic compounds and high yields of the products.

  3. The Reaction between Iron(II) Iodide and Potassium Dichromate(VI) in Acidified Aqueous Solution

    Science.gov (United States)

    Talbot, Christopher

    2013-01-01

    This "Science note" teaching lesson explores the possible reaction between the ions in a reaction mixture consisting of iron(II) iodide and potassium dichromate(VI) in acidified aqueous solution. The electrode potentials will be used to deduce any spontaneous reactions under standard thermodynamic conditions (298 K, 1 bar (approximately…

  4. Relaxation of the Silver/Silver Iodide Electrode in Aqueous Solution

    NARCIS (Netherlands)

    Peverelli, K.J.

    1979-01-01

    The aim of this study is to detect and characterize relaxation processes on silver/silver iodide electrodes in aqueous electrolyte solution. The information obtained is to be used for an estimation of the consequences of similar processes on colloidal AgI particles during encounter.In chapter 1 a ge

  5. Activation of lactoperoxidase by heme-linked protonation and heme-independent iodide binding.

    Science.gov (United States)

    Toyama, Akira; Tominaga, Aya; Inoue, Tatsuo; Takeuchi, Hideo

    2010-01-01

    Lactoperoxidase (LPO), a mammalian secretory heme peroxidase, catalyzes the oxidation of thiocyanate by hydrogen peroxide to produce hypothiocyanate, an antibacterial agent. Although LPO is known to be activated at acidic pH and in the presence of iodide, the structural basis of the activation is not well understood. We have examined the effects of pH and iodide concentration on the catalytic activity and the structure of LPO. Electrochemical and colorimetric assays have shown that the catalytic activity is maximized at pH 4.5. The heme Soret absorption band exhibits a small red-shift at pH 5.0 upon acidification, which is ascribable to a structural transition from a neutral to an acidic form. Resonance Raman spectra suggest that the heme porphyrin core is slightly contracted and the Fe-His bond is strengthened in the acidic form compared to the neutral form. The structural change of LPO upon activation at acidic pH is similar to that observed for myeloperoxidase, another mammalian heme peroxidase, upon activation at neutral pH. Binding of iodide enhances the catalytic activity of LPO without affecting either the optimum pH of activity or the heme structure, implying that the iodide binding occurs at a protein site away from the heme-linked protonation site.

  6. Distribution of bromine in mixed iodide-bromide organolead perovskites and its impact on photovoltaic performance

    NARCIS (Netherlands)

    Zhou, Yang; Wang, Feng; Fang, Hong-Hua; Loi, Maria Antonietta; Xie, Fang-Yan; Zhao, Ni; Wong, Ching-Ping

    2016-01-01

    Mixed iodide-bromide (I-Br) organolead perovskites are of great interest for both single junction and tandem solar cells since the optical bandgap of the materials can be tuned by varying the bromine to iodine ratio. Yet, it remains unclear how bromine incorporation modifies the properties of the pe

  7. Photoexcitation dynamics in solution-processed formamidinium lead iodide perovskite thin films for solar cell applications

    NARCIS (Netherlands)

    Fang, Hong-Hua; Wang, Feng; Adjokatse, Sampson; Zhao, Ni; Even, Jacky; Loi, Maria Antonietta

    2016-01-01

    Formamidinium lead iodide (FAPbI(3)) is a newly developed hybrid perovskite that potentially can be used in high-efficiency solution-processed solar cells. Here, the temperature-dependent dynamic optical properties of three types of FAPbI(3) perovskite films (fabricated using three different precurs

  8. Effects of continuous chlorination on entrained estuarine plankton

    Energy Technology Data Exchange (ETDEWEB)

    Erickson, S.J.; Foulk, H.R.

    1980-01-01

    Technical report: The effects of continuous chlorination in running sea water on entrained plankton were examined. The concentration of ATP was used as an indicator of biomass because: it is present in all living cells; the concentration is proportional to the living biomass; and dead cells lose ATP rapidly. Effects were measured by bioluminescence; luciferin-luciferase reagents from firefly lanterns were used to analyze ATP concentration. Results indicate that ATP measurement is an accurate, effective means of evaluating damage done to planktonic organisms by continuous chlorination. Further studies of the effects of low-concentration, continuous chlorination are recommended. (13 references, 1 table)

  9. Chlorine Dioxide Gas Treatment of Cantaloupe and Residue Analysis

    OpenAIRE

    Kaur, Simran

    2013-01-01

    Chlorine dioxide is a selective oxidant and powerful antimicrobial agent. Previous work has shown that treatment of cantaloupe with chlorine dioxide gas at 5 mg/L for 10 minutes results in a 4.6 and 4.3 log reduction of E. coli O157:H7 and L. monocytogenes respectively. A significant reduction (p Current analytical methods for chlorine dioxide and chloroxyanions are only applicable to aqueous samples. Some of these methods have been used to determine surface residues in treated products by...

  10. Experimental study on iodine chemistry (EXSI) - Containment experiments with methyl iodide

    Energy Technology Data Exchange (ETDEWEB)

    Holm, J.; Ekberg, C. (Chalmers Univ. of Technology, Goeteborg (Sweden)); Kaerkelae, T.; Auvinen, A. (VTT, Espoo (Finland)); Glaenneskog, H. (Vattenfall Power Consultant, Goeteborg (Sweden))

    2011-05-15

    An experimental study on radiolytic decomposition of methyl iodide was conducted in co-operation between VTT and Chalmers University of Technology as a part of the NKS-R programs. In year 2008 the NROI project, a Nordic collaboration studying iodine chemistry in the containment, was started. During year 2008 (NROI-1) the radiolytic oxidation of elemental iodine was investigated and during 2009 (NROI-2), the radiolytic oxidation of organic iodine was studied. This project (NROI-3) is a continuation of the investigation of the oxidation of organic iodine. The project has been divided into two parts. 1. The aims of the first part were to investigate the effect of ozone and UV-radiation, in dry and humid conditions, on methyl iodide. 2. The second project was about gamma radiation (approx20 kGy/h) and methyl iodide in dry and humid conditions. 1. Experimental results showed that the methyl iodide concentration in the facility was reduced with increasing temperature and increasing UV-radiation intensity. Similar behaviour occurred when ozone was present in the system. Formed organic gas species during the decomposition of methyl iodide was mainly formaldehyde and methanol. The particle formation was instant and extensive when methyl iodide was exposed to ozone and/or radiation at all temperatures. The size of the formed primary particles was about 10 nm and the size of secondary particles was between 50-200 nm. From the SEM-EDX analyses of the particles, the conclusion was drawn that these were some kind of iodine oxides (I{sub xO{sub y}). However, the correct speciation of the formed particles was difficult to obtain because the particles melted and fused together under the electron beam. 2. The results from this sub-project are more inconsistent and hard to interpret. The particle formation was significant lesser than corresponding experiments when ozone/UV-radiation was used instead of gamma radiation. The transport of gaseous methyl iodide through the facility was

  11. Chlorine-36 and chlorine concentrations within several compartments of a deciduous forest ecosystem in Meuse/Haute-Marne (France)

    Science.gov (United States)

    Pupier, Julie; Benedetti, Lucilla; Bourles, Didier; Leclerc, Elisabeth; Thiry, Yves

    2013-04-01

    Chlorine-36 is a cosmogenic nuclide mainly produced in the atmosphere by interactions between energetic particles originating from the cosmic radiations and 40Ar. Because of its long half-life (T1-2 = 3.01 105 yr) and its high mobility, chlorine-36 is a critical radionuclide concerning radioactive waste repository sites. Moreover, it has been shown that inorganic chlorine could be enriched along the trophic chain due to its high solubility and bioavailability (Ashworth and Shaw, 2006). Additionally, many studies during the last decades have established that due to chlorination process, organic chlorine may account for a large proportion of the total soil chlorine pool (more than 80 % in surface soils of temperate ecosystems. Redon et al., 2012). The aim of this study is thus to measure chlorine-36 in all the compartments of the biogeochemical cycle, to better understand its recycling in the biosphere. The study site is the experimental beech forest site of the Andra long-term monitoring and testing system (OPE*). It is located at Montiers-sur-Saulx, North-East of France and is associated to the future radioactive waste repository site of Bure. Since March 2012, rainwater above (rainfall collected from a 45 m high tower built on purpose) and below (throughfall and stemflow) the canopy, has been collected monthly, as well as soil solutions (gravitational and bound waters) at four depths (0, 10, 30, 60 cm deep). Chlorine-36 and chlorine have been measured in the rainfall samples between March and July 2012 and in water solutions collected from all compartments of the biosphere using isotope dilution mass spectrometry at the french AMS national facility ASTER located at CEREGE. The results yielded from the rainfall samples allow to study the temporal fluctuations of chlorine-36 in the atmosphere, which represents the main inflow of chlorine-36 in its biogeochemical cycle. The first results indicate a flow increase during the late spring-early summer. Santos et al

  12. Selective determination of chlorine dioxide using gas diffusion flow injection analysis

    Energy Technology Data Exchange (ETDEWEB)

    Hollowell, D.A.; Pacey, G.E.; Gordon, G.

    1985-12-01

    An automated absorbance technique for the determination of aqueous chlorine dioxide has been developed by utilizing gas diffusion flow injection analysis. A gas diffusion membrane is used to separate the donor (sampling) stream from the acceptor (detecting) stream. The absorbance of chlorine dioxide is monitored at 359 nm. The first method uses distilled water as the acceptor stream and gives a detection limit of 0.25 mg/L chlorine dioxide. This system is over 550 times more selective for chlorine dioxide than chlorine. To further minimize chlorine interference, oxalic acid is used in the acceptor stream. The detection limit for this system is 0.45 mg/L chlorine dioxide. This second system is over 5400 times more selective for chlorine dioxide than chlorine. Both methods show excellent selectivity for chlorine dioxide over iron and manganese compounds, as well as other oxychlorinated compounds such as chlorite and perchlorate ions. 18 references, 7 figures, 3 tables.

  13. RESEARCH ON MATHEMATICAL SIMULATION OF RESIDUAL CHLORINE DECAY AND OPTIMIZATION OF CHLORINATION ALLOCATION OF URBAN WATER DISTRIBUTION SYSTEM

    Institute of Scientific and Technical Information of China (English)

    TIAN Yi-mei; CHI Hai-yan; LI Hong; SHAN Jin-lin; ZHAI Chun-nian

    2005-01-01

    The concentration of Residual Chlorine (RC) frequently violates the standard in situations of urban water distribution system with large water supply area and long time of distribution.If chlorine dosage increases within water treatment plant, although RC in distribution system could meet water quality standard, Disinfection By-Products (DBPs) such as hydrocarbon halide rises.In the paper, a mathematical model of chlorine allocation optimization was presented based on reaction kinetics mechanism and optimization theory to solve the problem.The model includes the objective function of minimizing annual operation cost and constraints of RC standard and rational chlorination station distribution, and solving by 0-1 Integer Programming (IP).The model had been applied to a real water distribution system.The simulation results of the model showed that adding chlorine in water distribution system remarkably improved water quality and reduced the operation cost by 49.3% per year less than chlorine dosed only in water treatment plant to meet RC standard.The results prove adding chlorine in water distribution system based on the model can bring both technological and economic advancement.

  14. Conversion of Iodide to Hypoiodous Acid and Molecular Iodine at the Air-Water Interface

    Science.gov (United States)

    Pillar, E. A.; Guzman, M. I.

    2013-12-01

    Sea spray aerosols continuously transfer a significant amount of halides to the marine boundary layer, where they play a major role in the depletion of tropospheric ozone. The reactivity of iodide is of special interest in sea spray aerosols, where this species is enriched relative to chloride and bromide in surface seawater. This work presents laboratory experiments that provide mechanistic information to understand the reactivity of halides in atmospheric aerosols. Pneumatically assisted electrospray is used to aerosolize solutions of sodium iodide (0.01-100 μM), which are rapidly (~3 μs) oxidized by ozone at 25 °C. Reaction products include HIO, IO2-, IO3-, I2, HI2O-, and I3-, all identified by mass spectrometry. The distribution of products varies along two different reaction pathways, one favoring the production of I2 and HIO for typical tropospheric ozone levels (~50 ppbv), and another one directed to the production of IO3- at higher oxidizer concentrations. The formation of products increases exponentially with rising concentrations of initial sodium iodide, [NaI]0. The process is determined to be pH independent for the pH range 6-8 representative of surface waters. The substitution of aqueous solutions by organic solvents, such as methanol or acetonitrile, causes a decrease in the surface tension and lifetime of the droplets, leading to larger I2 production. The presence of surface active organic compounds, which alter the structure of the interfacial region, promote the pathway of I2 formation over IO3-. In conclusion, this presentation will show how the oxidation of iodide in aqueous microdroplets can release reactive gas-phase species, such as I2 and HIO, capable to affect tropospheric ozone globally. Normalized intensity of products observed during the ozonolysis of iodide solutions at 130 ppbv ozone. Cone voltage = 70 V, needle voltage = 2.5 kV.

  15. [The application of eosin and propidium iodide in evaluation of vitality of human spermatozoa].

    Science.gov (United States)

    Ploskonos, М В

    2014-11-01

    The article analyzes comparative assessment of vitality of spermatozoa by condition of permeability of membranes for eosin and propidium iodide and comparison of results acquired using technique of light and fluorescent microscopy. The comparison of data of light microscopy with eosin staining with data of fluorescent microscopy with propidium iodide staining demonstrated that percentage of content of spermatozoa separated from ejaculates of 28 fertile males and stained with eosin was reliably higher (34.8 ± 3.2) than percentage of content of spermatozoa with stained with propidium iodide (2.1 ± 4.0). After incubation of spermatozoa under room temperature during 24 hours percentage of unviable cells with stained eosin also was higher than in case of propidium iodide staining correspondingly (44.5 ± 3.3% and 34.7 ± 3.6%). The analysis of vitality of spermatozoa under damaging effect of oxidative stress on cell membrane developed by 4 hours incubation with 200 mkM of hydrogen peroxide (H2O2) demonstrated that under staining of spermatozoa with propidium iodide significantly higher percentage of damaged cells is detected. In such cases, eosin staining is less suitable for detection of vitality of spermatozoa (73.6 ± 5.8% against 51.7 ± 6.4%). The carried out experiment demonstrates that in case of detected effects on spermatozoa (for example, effect of oxidative stress) the light microscopy insufficiently adequate reflects degree of damage of membranes of spermatozoa. The fluorescent microscopy detects a higher percentage of spermatozoa with damaged membrane.

  16. Determining Residual Chlorine With Potassium iodide- Amylum Test paper%碘化钾-淀粉试纸法测定余氯

    Institute of Scientific and Technical Information of China (English)

    张万里

    2004-01-01

    基于余氯对碘化钾的氧化作用和碘淀粉反应,本文提出了测定余氯的碘化钾-淀粉试纸法.研究了最佳测试条件,用于测定医院污水中的余氯,获得了满意结果.测量范围为1.0-10.0mg/L.

  17. 碘化物对金精矿碘化浸出过程的影响%Effects of different iodides on gold concentrates leaching process in iodine­iodide solution

    Institute of Scientific and Technical Information of China (English)

    李绍英; 王海霞; 孙春宝; 赵留成; 阎志强

    2013-01-01

    Using the iodine­iodide leaching system, the effects of different iodides (ammonium iodide,potassium iodide, hydrogen iodide)on gold concentrates leaching process were discussed from the influence factors, such as initial iodine content, iodine and iodide ratio and solution pH value. The results show that, when ammonium iodide or potassium iodide is used as complex agent,under the conditions of initial iodine content of 1%, iodine and iodide molar ratio of 1:8, pH value of 7, liquid­solid ratio of 4:1, stirring speed of 600 r/min, leaching time of 4 h and temperature of 25℃, the gold leaching rates are around 90%;whereas the gold leaching effect is poorer when hydrogen iodide(aqueous solution is hydroiodic acid) is used as complex agent, and the gold leaching rate is only 75%. Considering the difference of leaching effect and availability of industry and so on,potassium iodide is the suitable complex reagent of gold concentrate leaching in iodine­iodide solution.%  采用碘−碘化物浸出体系,从碘初始含量、碘与碘化物摩尔比和浸出液pH值3个影响因素入手,考察不同碘化物(碘化铵、碘化钾和碘化氢)对金精矿碘化浸出过程的影响。结果表明:在碘初始含量为1%,碘与碘化物摩尔比为1:8,浸出液pH值为7,液固比为4:1,搅拌速度为600 r/min,浸出时间为4 h,温度为25℃的条件下,用碘化铵或碘化钾作为碘化浸金的络合剂,金的浸出率均能达到90%左右,而用碘化氢(其水溶液为氢碘酸)作络合剂时,金的浸出率仅有75%。考虑到不同碘化物浸金效果差异及工业应用的可行性等因素,确定碘化钾为适宜的金精矿碘化浸出络合剂。

  18. Inland Concentrations of Cl2 and ClNO2 in Southeast Texas Suggest Chlorine Chemistry Significantly Contributes to Atmospheric Reactivity

    Directory of Open Access Journals (Sweden)

    Cameron B. Faxon

    2015-10-01

    Full Text Available Measurements of molecular chlorine (Cl2, nitryl chloride (ClNO2, and dinitrogen pentoxide (N2O5 were taken as part of the DISCOVER-AQ Texas 2013 campaign with a High Resolution Time-of-Flight Chemical Ionization Mass Spectrometer (HR-ToF-CIMS using iodide (I- as a reagent ion. ClNO2 concentrations exceeding 50 ppt were regularly detected with peak concentrations typically occurring between 7:00 a.m. and 10:00 am. Hourly averaged Cl2 concentrations peaked daily between 3:00 p.m. and 4:00 p.m., with a 29-day average of 0.9 ± 0.3 (1σ ppt. A day-time Cl2 source of up to 35 ppt∙h−1 is required to explain these observations, corresponding to a maximum chlorine radical (Cl• production rate of 70 ppt∙h−1. Modeling of the Cl2 source suggests that it can enhance daily maximum O3 and RO2• concentrations by 8%–10% and 28%–50%, respectively. Modeling of observed ClNO2 assuming a well-mixed nocturnal boundary layer indicates O3 and RO2• enhancements of up to 2.1% and 38%, respectively, with a maximum impact in the early morning. These enhancements affect the formation of secondary organic aerosol and compliance with air quality standards for ozone and particulate matter.

  19. Complete Non-Radioactive Operability Tests for Cladding Hull Chlorination

    Energy Technology Data Exchange (ETDEWEB)

    Collins, Emory D [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Johnson, Jared A. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Hylton, Tom D. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Brunson, Ronald Ray [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Hunt, Rodney Dale [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); DelCul, Guillermo Daniel [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Bradley, Eric Craig [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Spencer, Barry B. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

    2016-04-01

    Non-radioactive operability tests were made to test the metal chlorination reactor and condenser and their accessories using batch chlorinations of non-radioactive cladding samples and to identify optimum operating practices and components that need further modifications prior to installation of the equipment into the hot cell for tests on actual used nuclear fuel (UNF) cladding. The operability tests included (1) modifications to provide the desired heating and reactor temperature profile; and (2) three batch chlorination tests using, respectively, 100, 250, and 500 g of cladding. During the batch chlorinations, metal corrosion of the equipment was assessed, pressurization of the gas inlet was examined and the best method for maintaining solid salt product transfer through the condenser was determined. Also, additional accessing equipment for collection of residual ash and positioning of the unit within the hot cell were identified, designed, and are being fabricated.

  20. Modeling of residual chlorine in water distribution system

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    Water quality within water distribution system may vary with both location and time. Water quality models are used to predict the spatial and temporal variation of water quality throughout water system. A model of residual chlorine decay in water pipe has been developed,given the consumption of chlorine in reactions with chemicals in bulk water, bio-films on pipe wall, in corrosion process, and the mass transport of chlorine from bulk water to pipe wall. Analytical methods of the flow path from water sources to the observed point and the water age of every observed node were proposed. Model is used to predict the decay of residual chlorine in an actual distribution system. Good agreement between calculated and measured values was obtained.

  1. Characters of chlorine isotopic composition in ocean water

    Digital Repository Service at National Institute of Oceanography (India)

    Xiao, Y.; Zhou, Y.; Liu, W.G.; Hong, A.; Wang, Q.; Wang, Y.; Wei, H.; Shirodkar, P.V.

    The chlorine isotopic composition of ocean water was determined using thermal ionization mass spectrometry based on the measurement of Cs sub(2) Cl sup(+) ion. The results show that the sup(37) Cl/ sup(35) Cl ratios are basically homogeneous...

  2. MULTISPECTRAL IDENTIFICATION OF CHLORINE DIOXIDE DISINFECTION BYPRODUCTS IN DRINKING WATER

    Science.gov (United States)

    This paper discusses the identification of organic disinfection byproducts (DBPs) at a pilot plant in Evansville, IN, which uses chlorine dioxide as a primary disinfectant. Unconventional multispectral identification techniques (gas chromatography combined with high- and low reso...

  3. MULTISPECTRAL IDENTIFICATION OF CHLORINE DIOXIDE BYPRODUCTS IN DRINKING WATER

    Science.gov (United States)

    This paper discusses the identification of organic disinfectant byproducts (DNPS) at a pilot plant in Evansville, IN, that uses chlorine dioxide as a primary disinfectant. nconventional multispectral identification techniques (gas chromatography combined with high- and low-resolu...

  4. Kinetics of Chlorine Decay in Water Distribution Systems

    Institute of Scientific and Technical Information of China (English)

    周建华; 薛罡; 赵洪宾; 汪永辉; 郭美芳

    2004-01-01

    A combined first and second-order model, which includes bulk decay and wall decay, was developed to describe chlorine decay in water distribution systems. In the model the bulk decay has complex relationships with total organic carbon (TOC), the initial chlorine concentration and the temperature. Except for the initial stages they can be simplified into a linear increase with TOC, a linear decrease with initial chlorine concentration and an exponential relationship with the temperature. The model also explains why chlorine decays rapidly in the initial stages. The parameters of model are determined by deriving the best fitness with experimental data. And the accuracy of model has been verified by using the experimental data and the monitoring data in a distribution system.

  5. Bioremediation of chlorinated ethenes in aquifer thermal energy storage

    NARCIS (Netherlands)

    Ni, Z.

    2015-01-01

      Subjects: bioremediation; biodegradation; environmental biotechnology, subsurface and groundwater contamination; biological processes; geochemistry; microbiology The combination of enhanced natural attenuation (ENA) of chlorinated volatile organic compounds (CVOCs) and aquife

  6. CHLORINE INACTIVATION OF CATEGORY "A" BIO-TERRORISM AGENTS

    Science.gov (United States)

    This poster presents information on the inactivation of select bioterrorist agents. Information will be presented on chlorine disinfection of vegetative cells of Brucella suis, Brucella melitensis, Burkholderia mallei, Burkholderia pseudomallei, Francisella tularensis and endos...

  7. Fate of free chlorine in drinking water during distribution in premise plumbing.

    Science.gov (United States)

    Zheng, Muzi; He, Chunguang; He, Qiang

    2015-12-01

    Free chlorine is a potent oxidizing agent and has been used extensively as a disinfectant in processes including water treatment. The presence of free chlorine residual is essential for the prevention of microbial regrowth in water distribution systems. However, excessive levels of free chlorine can cause adverse health effects. It is a major challenge to maintain appropriate levels of free chlorine residual in premise plumbing. As the first effort to assessing the fate of chlorine in premise plumbing using actual premise plumbing pipe sections, three piping materials frequently used in premise plumbing, i.e. copper, galvanized iron, and polyvinyl chloride (PVC), were investigated for their performance in maintaining free chlorine residual. Free chlorine decay was shown to follow first-order kinetics for all three pipe materials tested. The most rapid chlorine decay was observed in copper pipes, suggesting the need for higher chlorine dosage to maintain appropriate levels of free chlorine residual if copper piping is used. PVC pipes exhibited the least reactivity with free chlorine, indicative of the advantage of PVC as a premise plumbing material for maintaining free chlorine residual. The reactivity of copper piping with free chlorine was significantly hindered by the accumulation of pipe deposits. In contrast, the impact on chlorine decay by pipe deposits was not significant in galvanized iron and PVC pipes. Findings in this study are of great importance for the development of effective strategies for the control of free chlorine residual and prevention of microbiological contamination in premise plumbing.

  8. Silver-Catalyzed C(sp(3))-H Chlorination.

    Science.gov (United States)

    Ozawa, Jun; Kanai, Motomu

    2017-03-17

    A silver-catalyzed chlorination of benzylic, tertiary, and secondary C(sp(3))-H bonds was developed. The reaction proceeded with as low as 0.2 mol % catalyst loading at room temperature under air atmosphere with synthetically useful functional group compatibility. The regioselectivity and reactivity tendencies suggest that the chlorination proceeded through a radical pathway, but an intermediate alkylsilver species cannot be ruled out.

  9. Bromoform production in tropical open-ocean waters: OTEC chlorination

    Energy Technology Data Exchange (ETDEWEB)

    Hartwig, E.O.; Valentine, R.

    1981-09-01

    The bromoform, and other volatile organics produced while chlorinating both the evaporator and condenser seawater during operation of the one megawatt (1 MW) OTEC-1 test facility are reported. Although many halogenated compounds might be produced as a result of chlorination, the quantitative analyses in this study focused on volatile EPA priority pollutants. Bromoform is the compound specifically recognized as a potential pollutant. Its concentration may be indicative of other halogenated species.

  10. Assessment of the risk of transporting liquid chlorine by rail

    Energy Technology Data Exchange (ETDEWEB)

    Andrews, W.B.

    1980-03-01

    This report presents the risk of shipping liquid chlorine by rail. While chlorine is not an energy material, there are several benefits to studying chlorine transportation risks. First, chlorine, like energy materials, is widely used as a feedstock to industry. Second, it is the major purification agent in municipal water treatment systems and therefore, provides direct benefits to the public. Finally, other risk assessments have been completed for liquid chlorine shipments in the US and Europe, which provide a basis for comparison with this study. None of the previous PNL energy material risk assessments have had other studies for comparison. For these reasons, it was felt that a risk assessment of chlorine transportation by rail could provide information on chlorine risk levels, identify ways to reduce these risks and use previous studies on chlorine risks to assess the strengths and weaknesses of the PNL risk assessment methodology. The risk assessment methodology used in this study is summarized. The methodology is presented in the form of a risk assessment model which is constructed for ease of periodic updating of the data base so that the risk may be reevaluated as additional data become available. The report is sectioned to correspond to specific analysis steps identified in the model. The transport system and accident environment are described. The response of the transport system to accident environments is described. Release sequences are postulated and evaluated to determine both the likelihood and possible consequences of a release. Supportive data and analyses are given in the appendices. The risk assessment results are related to the year 1985 to allow a direct comparison with other reports in this series.

  11. SCENARIOS EVALUATION TOOL FOR CHLORINATED SOLVENT MNA

    Energy Technology Data Exchange (ETDEWEB)

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

    2006-08-16

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

  12. Shock-tube pyrolysis of chlorinated hydrocarbons - Formation of soot

    Science.gov (United States)

    Frenklach, M.; Hsu, J. P.; Miller, D. L.; Matula, R. A.

    1986-01-01

    Soot formation in pyrolysis of chlorinated methanes, their mixtures with methane, and chlorinated ethylenes were studied behind reflected shock waves by monitoring the attenuation of an He-Ne laser beam. An additional single-pulse shock-tube study was conducted for the pyrolysis of methane, methyl chloride, and dichloromethane. The experiments were performed at temperatures 1300-3000 K, pressures of 0.4-3.6 bar, and total carbon atom concentrations of 1-5 x 10 to the 17th atoms cu cm. The amounts of soot produced in the pyrolysis of chlorinated hydrocarbons are larger than that of their nonchlorinated counterparts. The sooting behavior and product distribution can be generally explained in terms of chlorine-catalyzed chemical reaction mechanisms. The pathway to soot from chlorinated methanes and ethylenes with high H:Cl ratio proceeds via the formation of C2H, C2H2, and C2H3 species. For chlorinated hydrocarbons with low H:Cl ratio, the formation of C2 and its contribution to soot formation at high temperatures becomes significant. There is evidence for the importance of CHCl radical and its reactions in the pyrolysis of dichloromethane.

  13. Prompt gamma analysis of chlorine in concrete for corrosion study

    Energy Technology Data Exchange (ETDEWEB)

    Naqvi, A.A. [Department of Physics, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia)]. E-mail: aanaqvi@kfupm.edu.sa; Nagadi, M.M. [Department of Physics, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Al-Amoudi, O.S.B. [Department of Civil Engineering, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia)

    2006-02-15

    Measurement of chlorine in concrete is very important for studying of corrosion of reinforcing steel in concrete. Corrosion of reinforcing steel is primarily ascribed to the penetration of chloride ions to the steel surface. Preventive measures for avoiding concrete structure reinforcement corrosion requires monitoring the chloride ion concentration in concrete so that its concentration does not exceed a threshold limit to initiate reinforcement concrete corrosion. An accelerator based prompt gamma neutron activation analysis (PGNAA) setup has been developed for non-destructive analysis of elemental composition of concrete samples. The setup has been used to measure chlorine concentration in concrete samples over a 1-3 wt% concentration range. Although a strong interference has been observed between the chlorine {gamma}-rays and calcium {gamma}-rays from concrete, the chlorine concentration in concrete samples has been successfully measured using the 1.164 and 7.643 MeV chlorine {gamma}-rays. The experimental data were compared with the results of the Monte Carlo simulations. An excellent agreement has been achieved between the experimental data and results of Monte Carlo simulations. The study has demonstrated the successful use of the accelerator-based PGNAA setup in non-destructive analysis of chlorine in concrete samples.

  14. Prompt gamma analysis of chlorine in concrete for corrosion study.

    Science.gov (United States)

    Naqvi, A A; Nagadi, M M; Al-Amoudi, O S B

    2006-02-01

    Measurement of chlorine in concrete is very important for studying of corrosion of reinforcing steel in concrete. Corrosion of reinforcing steel is primarily ascribed to the penetration of chloride ions to the steel surface. Preventive measures for avoiding concrete structure reinforcement corrosion requires monitoring the chloride ion concentration in concrete so that its concentration does not exceed a threshold limit to initiate reinforcement concrete corrosion. An accelerator based prompt gamma neutron activation analysis (PGNAA) setup has been developed for non-destructive analysis of elemental composition of concrete samples. The setup has been used to measure chlorine concentration in concrete samples over a 1-3 wt% concentration range. Although a strong interference has been observed between the chlorine gamma-rays and calcium gamma-rays from concrete, the chlorine concentration in concrete samples has been successfully measured using the 1.164 and 7.643 MeV chlorine gamma-rays. The experimental data were compared with the results of the Monte Carlo simulations. An excellent agreement has been achieved between the experimental data and results of Monte Carlo simulations. The study has demonstrated the successful use of the accelerator-based PGNAA setup in non-destructive analysis of chlorine in concrete samples.

  15. Chlorine dioxide project allows Stora to clean up, use hardwoods

    Energy Technology Data Exchange (ETDEWEB)

    Butters, G.

    1988-10-01

    Effluent fouling into the Strait of Canso between Nova Scotia mainland and Cape Breton Island has caused Stora Forest Industries Ltd. to develop a $5.6 million solution to its chlorine and acid problems. In 1987, Stora produced about 160,000 tonnes of market pulp where their resource base increasingly consisted of hardwood. The company uses hardwood chips for a growing percentage of its annual pulp production and for its hog fuel boiler, but became faced with having to use more local hardwoods which contributes to the resin problem. Their solution was to construct a 12-tpd chlorine dioxide generator, a process using dry sodium chlorate added to concentrated H/sub 2/SO/sub 4/, The products are chlorine dioxide and highly concentrated sulphuric acid resulting from the elimination of water at the starting point. This will eliminate the acid effluent from the generator and the sulphuric acid will be recycled to the top of the chlorine dioxide generation process. In the new process, ClCO/sub 2/ replaces 70% of the chlorine in the first stage, with 100% substitution a goal. In addition to eliminating the chlorine, other benefits include an increase in pulp production, a nominal increase in pulp strength, lower production costs, and an economic incentive to harvest the area's mixed-wood stands.

  16. Zebra mussel control using periodic chlorine dioxide treatments

    Energy Technology Data Exchange (ETDEWEB)

    Tsou, J. [Electric Power Research Institute, Palo Alto, CA (United States); Coyle, J. [Central Illinois Public Service, Merdosia, IL (United States); Crone, D. [Illinois Power Company, Alton, IL (United States)] [and others

    1996-08-01

    This paper summarizes the EPRI report (TR-105202) on the same topic as well as presents changes in current thinking on the suitability (applicability) of chlorine dioxide for fouling control. Chlorine dioxide was tested as a zebra mussel biocide at two steam electric generating stations in Illinois and one in Indiana. The purpose of these studies was to determine the efficacy of chlorine dioxide in killing zebra mussels and to develop site specific treatment programs for the three utilities. The Electric Power Research Institute (EPRI) Zebra Mussel Consortium sponsored the testing of this recent use of chlorine dioxide. The raw water system at Central Illinois Public Service`s Meredosia Station, on the Illinois River, received applications of chlorine dioxide in April, July, and September 1994. The raw water system at Illinois Power Company`s Wood River Station, on the Mississippi River, received applications in July 1993, January, April, May, July, and September 1994. The Gallagher Station, on the Ohio River, was treated in July and October 1994. Chlorine dioxide was generated on-site and injected into the water intake structure. Both cooling and service water systems were treated at the facilities. 6 refs., 13 figs.

  17. Chlorobenzene outputs from combustion of chlorinated organic and inorganic compounds

    Energy Technology Data Exchange (ETDEWEB)

    Green, A.E.S.; Vitali, J.A.; Miller, T.L. [Univ. of Florida, Gainesville, FL (United States)

    1994-12-31

    The authors consider the gas phase formation of chlorinated benzenes and phenols as precursors of chlorinated dioxins and furans from the combustion of solid fuels containing organically bound chlorine. The model investigated is intended to apply to the combustion of medical waste, municipal waste and coals containing chlorine. Assuming a temperature-time profile drawn from incinerator experiments, the authors use kinetic modeling with known reaction rates to further investigate four models of chlorinated benzene formation. Since reaction rates for most chlorination processes are now known, the authors choose simple systems of reaction rates that yield outputs that can be made approximately compatible with results of the Pittsfield-Vicon incinerator and Clean Combustion Technology Laboratory experiments. The authors also consider recent measurements of HCI emissions from crematoria and the implication of this work with respect to the benefits of material substitution in medical and municipal waste incineration. These benefits should also accompany the dechlorination of coals. The authors note the disparity between the prevailing USA position and the emerging position of Germany on the issue of halogenated plastics. The authors also note that Europe and Asia are beginning to address solid fuel issues as a consolidated discipline. This pattern should be helpful in broadening the understanding of solid fuels combustion processes and in ferreting out erroneous data and conclusions. This is important in view of the recent concern about the role of low dioxin exposure levels on fetal development and the immune system.

  18. Disinfection of swine wastewater using chlorine, ultraviolet light and ozone.

    Science.gov (United States)

    Macauley, John J; Qiang, Zhimin; Adams, Craig D; Surampalli, Rao; Mormile, Melanie R

    2006-06-01

    Veterinary antibiotics are widely used at concentrated animal feeding operations (CAFOs) to prevent disease and promote growth of livestock. However, the majority of antibiotics are excreted from animals in urine, feces, and manure. Consequently, the lagoons used to store these wastes can act as reservoirs of antibiotics and antibiotic-resistant bacteria. There is currently no regulation or control of these systems to prevent the spread of these bacteria and their genes for antibiotic resistance into other environments. This study was conducted to determine the disinfection potential of chlorine, ultraviolet light and ozone against swine lagoon bacteria. Results indicate that a chlorine dose of 30 mg/L could achieve a 2.2-3.4 log bacteria reduction in lagoon samples. However, increasing the dose of chlorine did not significantly enhance the disinfection activity due to the presence of chlorine-resistant bacteria. The chlorine resistant bacteria were identified to be closely related to Bacillus subtilis and Bacillus licheniformis. A significant percentage of lagoon bacteria were not susceptible to the four selected antibiotics: chlortetracycline, lincomycin, sulfamethazine and tetracycline (TET). However, the presence of both chlorine and TET could inactivate all bacteria in one lagoon sample. The disinfection potential of UV irradiation and ozone was also examined. Ultraviolet light was an effective bacterial disinfectant, but was unlikely to be economically viable due to its high energy requirements. At an ozone dose of 100 mg/L, the bacteria inactivation efficiency could reach 3.3-3.9 log.

  19. Radioactive iodide (131 I-) excretion profiles in response to potassium iodide (KI) and ammonium perchlorate (NH4ClO4) prophylaxis.

    Science.gov (United States)

    Harris, Curtis; Dallas, Cham; Rollor, Edward; White, Catherine; Blount, Benjamin; Valentin-Blasini, Liza; Fisher, Jeffrey

    2012-08-01

    Radioactive iodide ((131)I-) protection studies have focused primarily on the thyroid gland and disturbances in the hypothalamic-pituitary-thyroid axis. The objective of the current study was to establish (131)I- urinary excretion profiles for saline, and the thyroid protectants, potassium iodide (KI) and ammonium perchlorate over a 75 hour time-course. Rats were administered (131)I- and 3 hours later dosed with either saline, 30 mg/kg of NH(4)ClO(4) or 30 mg/kg of KI. Urinalysis of the first 36 hours of the time-course revealed that NH(4)ClO(4) treated animals excreted significantly more (131)I- compared with KI and saline treatments. A second study followed the same protocol, but thyroxine (T(4)) was administered daily over a 3 day period. During the first 6-12 hour after (131)I- dosing, rats administered NH(4)ClO(4) excreted significantly more (131)I- than the other treatment groups. T(4) treatment resulted in increased retention of radioiodide in the thyroid gland 75 hour after (131)I- administration. We speculate that the T(4) treatment related reduction in serum TSH caused a decrease synthesis and secretion of thyroid hormones resulting in greater residual radioiodide in the thyroid gland. Our findings suggest that ammonium perchlorate treatment accelerates the elimination rate of radioiodide within the first 24 to 36 hours and thus may be more effective at reducing harmful exposure to (131)I- compared to KI treatment for repeated dosing situations. Repeated dosing studies are needed to compare the effectiveness of these treatments to reduce the radioactive iodide burden of the thyroid gland.

  20. Purification of highly chlorinated dioxins degrading enzyme

    Energy Technology Data Exchange (ETDEWEB)

    Ishii, K.; Furuichi, T.; Koike, K.; Kuboshima, M. [Hokkaido Univ. (Japan). Division of Environment Resource Engineering, Graduate School of Engineering

    2004-09-15

    Soil contamination caused by dioxins in and around sites of incinerators for municipal solid waste (MSW) is a concern in Japan. For example, scattering wastewater from a wet gas scrubber at an MSW incinerator facility in Nose, Osaka caused soil and surface water contamination. The concentration of dioxins in the soil was about 8,000 pg-TEQ/g. Other contamination sites include soils on which fly ash has been placed directly or improperly stored and landfill sites that have received bottom and fly ash over a long period. Some countermeasures are required immediately at these dioxins-contaminated sites. We have previously developed bioreactor systems for dioxin-contaminated water and soil. We have shown that a fungus, Pseudallescheria boydii (P. boydii), isolated from activated sludge treating wastewater that contained dioxins, has the ability to degrade highly chlorinated dioxins. A reaction product of octachlorinated dibenzo-p-dioxin (OCDD) was identified as heptachlorinated dibenzo-p-dioxin. Therefore, one of the pathways for degradation of OCDD by this fungus was predicted to be as follows: OCDD is transformed by dechlorination and then one of the remaining aromatic rings is oxidized. To apply P. boydii to on-site technologies (e.g., bioreactor systems), as well as in situ technologies, enzyme treatment using a dioxin-degrading enzyme from P. boydii needs to be developed because P. boydii is a weak pathogenic fungus, known to cause opportunistic infection. As a result, we have studied enzyme purification of nonchlorinated dioxin, namely, dibenzo-pdioxin (DD). However, we did not try to identify enzymes capable of degrading highly chlorinated dioxins. This study has elucidated a method of enzyme assay for measuring OCDD-degrading activity, and has attempted to purify OCDD-degrading enzymes from P. boydii using enzyme assay. In addition, as first step toward purifying 2,3,7,8-tetrachlorodibenzo-p-dioxin (2,3,7,8-TCDD), 2,3,7,8-TCDD degradation tests were carried out

  1. Synergistic effect between UV and chlorine (UV/chlorine) on the degradation of carbamazepine: Influence factors and radical species.

    Science.gov (United States)

    Wang, Wen-Long; Wu, Qian-Yuan; Huang, Nan; Wang, Ting; Hu, Hong-Ying

    2016-07-01

    For successful wastewater reclamation, advanced oxidation processes have attracted attention for elimination of emerging contaminants. In this study, the synergistic treatment with UV irradiation and chlorine (UV/chlorine) was used to degrade carbamazepine (CBZ). Neither UV irradiation alone nor chlorination alone could efficiently degraded CBZ. UV/chlorine oxidation showed a significant synergistic effect on CBZ degradation through generation of radical species (OH and Cl), and this process could be well depicted by pseudo first order kinetic. The degradation rate constants (kobs,CBZ) of CBZ increased linearly with increasing UV irradiance and chlorine dosage. The degradation of CBZ by UV/chlorine in acidic solutions was more efficient than that in basic solutions mainly due to the effect of pH on the dissociation of HOCl and OCl(-) and then on the quantum yields and radical species quenching of UV/chlorine. When pH was increased from 5.5 to 9.5, the rate constants of degradation of CBZ by OH decreased from 0.65 to 0.14 min(-1) and that by Cl decreased from 0.40 to 0.11 min(-1). The rate constant for the reaction between Cl and CBZ was 5.6 ± 1.6 × 10(10) M(-1) s(-1). Anions of HCO3(-) (1-50 mM) showed moderate inhibition of CBZ degradation by UV/chlorine, while Cl(-) did not. UV/chlorine could efficiently degrade CBZ in wastewater treatment plant effluent, although the degradation was inhibited by about 30% compared with that in ultrapure water with chlorine dosage of 0.14-0.56 mM. Nine main oxidation products of the CBZ degradation by UV/chlorine were identified using the HPLC-QToF MS/MS. Initial oxidation products arose from hydroxylation, carboxylation and hydrogen atom abstraction of CBZ by OH and Cl, and were then further oxidized to generate acylamino cleavage and decarboxylation products of acridine and acridione.

  2. Inactivation of antibiotic resistance genes in municipal wastewater effluent by chlorination and sequential UV/chlorination disinfection

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Yingying; Zhuang, Yao; Geng, Jinju, E-mail: jjgeng@nju.edu.cn; Ren, Hongqiang, E-mail: hqren@nju.edu.cn; Zhang, Yan; Ding, Lili; Xu, Ke

    2015-04-15

    This study investigated disinfection methods including chlorination, ultraviolet (UV) irradiation and sequential UV/chlorination treatment on the inactivation of antibiotic resistance genes (ARGs). ARGs including sul1, tetX, tetG, intI1, and 16S rRNA genes in municipal wastewater treatment plant (MWTP) effluent were examined. The results indicated a positive correlation between the removal of ARGs and chlorine dosage (p = 0.007–0.014, n = 6),as well as contact time (p = 0.0001, n = 10). Greater free chlorine (FC) dosage leads to higher removal for all the genes and the maximum removal (1.30–1.49 logs) could be achieved at FC dosage of 30 mg L{sup −1}. The transformation kinetic data for ARGs removal (log C{sub 0} / C) followed the second-order reaction kinetic model with FC dosage (R{sup 2} = 0.6829–0.9999) and contact time (R{sup 2} = 0.7353–8634), respectively. Higher ammonia nitrogen (NH{sub 3}–N) concentration was found to lead to lower removal of ARGs at the same chlorine dosage. When the applied Cl{sub 2}:NH{sub 3}–N ratio was over 7.6:1, a significant reduction of ARGs (1.20–1.49 logs) was achieved. By using single UV irradiation, the log removal values of tetX and 16Ss rRNA genes were 0.58 and 0.60, respectively, while other genes were 0.36–0.40 at a fluence of 249.5 mJ cm{sup −2}, which was observed to be less effective than chlorination. With sequential UV/chlorination treatment, 0.006 to 0.31 log synergy values of target genes were observed under different operation parameters. - Highlights: • Chlorine is more effective than UV irradiation in removing ARGs from MWTP effluent. • The chlorination reaction followed the second-order reaction kinetic model. • Higher NH{sub 3}–N contents result in lower ARGs removal in the chlorination process. • FC is more effective than CC on the inactivation of ARGs. • UV irradiation followed by chlorination shows high efficiency in removing ARGs.

  3. Site-selective photofragmentation of chlorinated polymeric films observed around the chlorine K-edge

    Energy Technology Data Exchange (ETDEWEB)

    Arantes, C., E-mail: csilva@inmetro.gov.br [Divisão de Metrologia de Materiais, Instituto Nacional de Metrologia, Qualidade e Tecnologia, Xerém 25250-020, Duque de Caxias, RJ (Brazil); Mendes, L.A.V. [Instituto de Física, Universidade Federal da Bahia, Ondina, 40210-340 Salvador, BA (Brazil); Pinho, R.R. [Departamento de Física-ICE, Universidade Federal de Juiz de Fora, Campus Universitário, 36036-330 Juiz de Fora, MG (Brazil); Ferreira, M. [PEMM/COPPE, Universidade Federal do Rio de Janeiro, Cidade Universitária, Ilha do Fundão, 21941-972 Rio de Janeiro, RJ (Brazil); Souza, G.G.B. de; Rocha, A.B.; Rocco, M.L.M. [Instituto de Química, Universidade Federal do Rio de Janeiro, Cidade Universitária, Ilha do Fundão, 21941-909 Rio de Janeiro, RJ (Brazil)

    2013-03-29

    Highlights: ► PVC and PVDC were studied by PSID and NEXAFS techniques at the Chlorine 1s-edge. ► PVC film presented isotope ratio of 3:1 in the PSID spectrum. ► Cl{sup +} ion yield curves reproduce the photoabsorption spectrum for both polymers. ► Site-selectivity of C–Cl bond breaking due to an efficient spectator Auger decay. - Abstract: Photon stimulated ion desorption (PSID) and Near-edge X-ray absorption fine structure (NEXAFS) studies have been performed on poly(vinyl chloride) (PVC) and poly(vinyl dichloride) (PVDC) around the chlorine 1s-edge. Experiments were performed using a synchrotron source operating in the single-bunch mode and a time-of-flight mass spectrometry for ion analysis. Cl{sup +} ion yields, as a function of the photon energy, reproduce the photoabsorption spectrum, showing significant increase at the 1s-resonance. Edge-jump ratios, defined as the ratio between edge-jumps (intensity ratio of the yields between above and below the absorption edge) of two different transitions, for Cl{sup +} ion yields were much higher than the equivalent electron yields, indicating site-selectivity in C–Cl bond breaking for both polymers, as a result of efficient spectator Auger decay. The expected isotope ratio of 3:1 for chlorine was measured for PVC. The interpretation of the NEXAFS spectrum was assisted by quantum mechanical calculations at a multireference perturbation theory level.

  4. Experimental study on iodine chemistry (EXSI) - Containment experiments with methyl iodide

    Energy Technology Data Exchange (ETDEWEB)

    Holm, J.; Glaenneskog, H.; Ekberg, C. (Chalmers Univ. of Technology (Sweden)); Kaerkelae, T.; Auvinen, A. (VTT Technical Research Centre of Finland (Finland))

    2010-05-15

    An experimental study on radiolytic decomposition of methyl iodide was conducted in co-operation between VTT and Chalmers University of Technology as a part of the NKS-R programs. The behaviour of iodine during a severe accident has been studied in several experimental programs, ranging from the large-scale PHEBUS FP tests and intermediate-scale ThAI tests to numerous separate effect studies. In year 2008 the NROI project, a Nordic collaboration studying iodine chemistry in the containment was started. During 2009, oxidation of iodine, especially organic iodine, was studied within the NROI project. The chemistry of organic iodine in the gas phase is still one of the greatest remaining uncertainties concerning iodine behaviour during a severe accident. During the first year of the NROI project the oxidation of elemental iodine, I2, with ozone and UV-light was investigated. In this study organic iodide, in this case methyl iodide, was investigated in similar conditions as in the NROI-1 project. The experimental facility applied in this study is based on the sampling system built at VTT for the ISTP project CHIP conducted by IRSN. The experimental facility and the measuring technology are sophisticated and unique in the area of nuclear research as well as in the field of aerosol science. Experimental results showed that the methyl iodide concentration in the facility was reduced with increasing temperature and increasing UVC intensity. Similar behaviour occurred when ozone was present in the system. Formed organic gas species during the decomposition of methyl iodide was mainly formaldehyde and methanol. Instant and extensive particle formation occurred when methyl iodide was transported through a UVC radiation field and/or when ozone was present. The size of the formed primary particles was about 10 nm and the size of secondary particles was between 50-150 nm. From the SEM-EDX analyses of the particles, the conclusion was drawn that these were some kind of iodine

  5. Ficusmicrochlorin A-C, two new methoxy lactone chlorins and an anhydride chlorin from the leaves of Ficus microcarpa.

    Science.gov (United States)

    Lin, Huan-You; Chiu, Hsi-Lin; Lu, Te-Ling; Tzeng, Chih-Ying; Lee, Tzong-Huei; Lee, Ching-Kuo; Shao, Yi-Yuan; Chen, Chiy-Rong; Chang, Chi-I; Kuo, Yueh-Hsiung

    2011-01-01

    Two new methoxy lactone chlorins ficusmicrochlorin A (1) and ficusmicrochlorin B (2), and one new anhydride chlorin ficusmicrochlorin C (3), along with eight known pheophytins were isolated from the leaves of Ficus microcarpa. Their structures were determined by the extensive 1D- and 2D-NMR techniques. New pheophytin compound was rarely obtained from natural sources. In the past ten years, only three new natural pheophytins were characterized.

  6. Transformation of cefazolin during chlorination process: products, mechanism and genotoxicity assessment.

    Science.gov (United States)

    Li, Liping; Wei, Dongbin; Wei, Guohua; Du, Yuguo

    2013-11-15

    Large quantities of cephalosporins have entered into aquatic environment in recent years, posing potential adverse effect to human health and ecological safety. In this study, cefazolin, one of widely used cephalosporins, was targeted to explore its transformation behaviors in chlorination disinfection process. With the help of ultra high performance liquid chromatography and high resolution mass spectroscopy, one chlorinated product and four oxidation products were detected in cefazolin chlorination system. The corresponding transformation pathways of cefazolin were proposed. Two kinds of reactions occurred in chlorination system, one was oxidation of thioether-sulfur to sulfoxide and di-sulfoxide, and the other was base-catalyzed electrophilic substitution of alpha-H of amide by chlorine atom. The pH value determined the occurrence of reaction types, and increasing chlorine dose promoted transformation of cefazolin. More importantly, genotoxicity in SOS/umu assay had an elevation after chlorination, which might be attributed to the formation of chlorinated product and sulfoxide during chlorination process.

  7. Electrochemical Membrane Reactors for Sustainable Chlorine Recycling

    Science.gov (United States)

    Vidakovic-Koch, Tanja; Martinez, Isai Gonzalez; Kuwertz, Rafael; Kunz, Ulrich; Turek, Thomas; Sundmacher, Kai

    2012-01-01

    Polymer electrolyte membranes have found broad application in a number of processes, being fuel cells, due to energy concerns, the main focus of the scientific community worldwide. Relatively little attention has been paid to the use of these materials in electrochemical production and separation processes. In this review, we put emphasis upon the application of Nafion membranes in electrochemical membrane reactors for chlorine recycling. The performance of such electrochemical reactors can be influenced by a number of factors including the properties of the membrane, which play an important role in reactor optimization. This review discusses the role of Nafion as a membrane, as well as its importance in the catalyst layer for the formation of the so-called three-phase boundary. The influence of an equilibrated medium on the Nafion proton conductivity and Cl− crossover, as well as the influence of the catalyst ink dispersion medium on the Nafion/catalyst self-assembly and its importance for the formation of an ionic conducting network in the catalyst layer are summarized. PMID:24958294

  8. Chlorinated hydrocarbon contaminants in arctic marine mammals.

    Science.gov (United States)

    Norstrom, R J; Muir, D C

    1994-09-16

    By 1976, the presence of chlorinated hydrocarbon contaminants (CHCs) had been demonstrated in fur seal (Callorhinus ursinus), ringed seal (Phoca hispida), hooded seal (Cystophora cristata), bearded seal (Erignathus barbatus), walrus (Obdobenus rosmarus divergens), beluga (Delphinapterus leucas), porpoise (Phocoena phocoena) and polar bear (Ursus maritimus) in various parts of the Arctic. In spite of this early interest, very little subsequent research on contaminants in Arctic marine mammals was undertaken until the mid-1980s. Since that time, there has been an explosion of interest, resulting in a much expanded data base on contaminants in Arctic marine mammals. Except in the Russian Arctic, data have now been obtained on the temporospatial distribution of PCBs and other contaminants in ringed seal, beluga and polar bear. Contaminants in narwhal (Monodon monoceros) have also now been measured. On a fat weight basis, the sum of DDT-related compounds (S-DDT) and PCB levels are lowest in walrus (St. Lawrence and ringed seal in the Baltic Sea, indicate that overall contamination of the Arctic marine ecosystem is 10-50 times less than the most highly contaminated areas in the northern hemisphere temperate latitude marine environment. Geographic distribution of residue levels in polar bears indicates a gradual increase from Alaska east to Svalbard, except PCB levels are significantly higher in eastern Greenland and Svalbard. Information on temporal trends is somewhat contradictory.(ABSTRACT TRUNCATED AT 400 WORDS)

  9. Electrochemical Membrane Reactors for Sustainable Chlorine Recycling

    Directory of Open Access Journals (Sweden)

    Ulrich Kunz

    2012-07-01

    Full Text Available Polymer electrolyte membranes have found broad application in a number of processes, being fuel cells, due to energy concerns, the main focus of the scientific community worldwide. Relatively little attention has been paid to the use of these materials in electrochemical production and separation processes. In this review, we put emphasis upon the application of Nafion membranes in electrochemical membrane reactors for chlorine recycling. The performance of such electrochemical reactors can be influenced by a number of factors including the properties of the membrane, which play an important role in reactor optimization. This review discusses the role of Nafion as a membrane, as well as its importance in the catalyst layer for the formation of the so-called three-phase boundary. The influence of an equilibrated medium on the Nafion proton conductivity and Cl crossover, as well as the influence of the catalyst ink dispersion medium on the Nafion/catalyst self-assembly and its importance for the formation of an ionic conducting network in the catalyst layer are summarized.

  10. Development of a Site-Specific Kinetic Model for Chlorine Decay and the Formation of Chlorination By-Products in Seawater

    Directory of Open Access Journals (Sweden)

    Suhur Saeed

    2015-07-01

    Full Text Available Chlorine is used commonly to prevent biofouling in cooling water systems. The addition of chlorine poses environmental risks in natural systems due to its tendency to form chlorination by-products (CBPs when exposed to naturally-occurring organic matter (NOM. Some of these CBPs can pose toxic risks to aquatic and benthic species in the receiving waters. It is, therefore, important to study the fate of residual chlorine and CBPs to fully understand the potential impacts of chlorination to the environment. The goal of this study was to develop improved predictions of how chlorine and CBP concentrations in seawater vary with time, chlorine dose and temperature. In the present study, chlorination of once-through cooling water at Ras Laffan Industrial City (RLIC, Qatar, was studied by collecting unchlorinated seawater from the RLIC cooling water system intake, treating it with chlorine and measuring time series of chlorine and CBP concentrations. Multiple-rate exponential curves were used to represent fast and slow chlorine decay and CBP formation, and site-specific chlorine kinetic relationships were developed. Through extensive analysis of laboratory measurements, it was found that only some of the control parameters identified in the literature were important for predicting residual chlorine and CBP concentrations for this specific location. The new kinetic relationships were able to significantly improve the predictability and validity of Generalized Environmental Modeling System for Surfacewaters (GEMSS-chlorine kinetics module (CKM, a three-dimensional hydrodynamic and chlorine kinetics and transport model when applied for RLIC outfall studies using actual field measurements.

  11. Cooperative effect of silver in copper-catalyzed trifluoromethylation of aryl iodides using Me3SiCF3

    KAUST Repository

    Weng, Zhiqiang

    2011-06-13

    An effective model of cooperative effect of silver for the coppercatalyzed trifluoromethylation of activated and unactivated aryl iodides to trifluoromethylated arenes using Me3SiCF3 was achieved with a broad substrate scope. © 2011 American Chemical Society.

  12. Formation of iodinated disinfection by-products during oxidation of iodide-containing water with potassium permanganate.

    Science.gov (United States)

    Ye, Tao; Xu, Bin; Lin, Yi-Li; Hu, Chen-Yan; Xia, Sheng-Ji; Lin, Lin; Mwakagenda, Seleli Andrew; Gao, Nai-Yun

    2012-11-30

    This study shows that iodinated disinfection by-products (I-DBPs) including iodoform (IF), iodoacetic acid (IAA) and triiodoacetic acid (TIAA) can be produced when iodide-containing waters are in contact with potassium permanganate. IF was found as the major I-DBP species during the oxidation. Iodide was oxidized to HOI, I(2) and I(3)(-), consequently, which led to the formation of iodinated organic compounds. I-DBPs varied with reaction time, solution pH, initial concentrations of iodide and potassium permanganate. Yields of IF, IAA and TIAA increased with reaction time and considerable I-DBPs were formed within 12 h. Peak IF yields were found at circumneutral pH range. However, formation of IAA and TIAA was favored under acidic conditions. Molar ratio of iodide to potassium permanganate showed significant influence on formation of IF, IAA and TIAA. The formation of IF, IAA and TIAA also depended on the characteristics of the waters.

  13. Gap energy studied by optical transmittance in lead iodide monocrystals grown by Bridgman's Method

    Directory of Open Access Journals (Sweden)

    Veissid N.

    1999-01-01

    Full Text Available The bandgap energy as a function of temperature has been determined for lead iodide. The monocrystal was obtained in a vacuum sealed quartz ampoule inside a vertical furnace by Bridgman's method. The optical transmittance measurement enables to evaluate the values of Eg. By a fitting procedure of Eg as a function of temperature is possible to extract the parameters that govern its behavior. The variation of Eg with temperature was determined as: Eg(T = Eg(0 - aT2/(a + T, with: Eg(0 = (2.435 ± 0.008 eV, a = (8.7 ± 1.3 x 10-4 eV/K and a = (192 ± 90 K. The bandgap energy of lead iodide at room temperature was found to be 2.277 ± 0.007 eV.

  14. Induction of iodide uptake in transformed thyrocytes: a compound screening in cell lines

    Energy Technology Data Exchange (ETDEWEB)

    Froehlich, Eleonore [University of Tuebingen, Department of Endocrinology, Metabolism, Nephrology and Clinical Chemistry, Internal Medicine, Tuebingen (Germany); Brossart, Peter [University of Tuebingen, Department of Haematology, Oncology, Immunology and Rheumatology, Internal Medicine, Tuebingen (Germany); Wahl, Richard [University of Tuebingen, Department of Endocrinology, Metabolism, Nephrology and Clinical Chemistry, Internal Medicine, Tuebingen (Germany); Department IV, Internal Medicine, Tuebingen (Germany)

    2009-05-15

    Retinoic acid presently is the most advanced agent able to improve the efficacy of radioiodine therapy in differentiated thyroid carcinoma. In order to identify compounds with higher efficacy a panel of pharmacologically well-characterized compounds with antitumour action in solid cancer cell lines was screened. The effects of the compounds on iodide uptake, cell number, proliferation and apoptosis were evaluated. In general, compounds were more effective in cell lines derived from more aggressive tumours. The effectiveness in terms of number of responsive cell lines and maximal increase in iodide uptake achieved decreased in the order: APHA > valproic acid {approx} sirolimus {approx} arsenic trioxide > retinoic acid {approx} lovastatin > apicidine {approx} azacytidine {approx} retinol {approx} rosiglitazone {approx} bortezomib. We hypothesize that testing of cells from primary tumours or metastases in patients may be a way to identify compounds with optimum therapeutic efficacy for individualized treatment. (orig.)

  15. Preparation,Characterization and Optical Properties of Hostguest Nanocomposite Material Mordenite—silver Iodide

    Institute of Scientific and Technical Information of China (English)

    ZHAIQing-zhou; QIUShi-lun

    2003-01-01

    Silver iodide nanoclusters were successfully prepared in the channels of mordenite by a heat diffusion method.Powder X-ray diffraction.adsorption technique and infrared spectroscopy were used to characterize the prepared materials,which showed that the guest silver iodied had been encapsulated in the channels of mordenite.The optical properties of the solid phase diffuse reflectance absorption of nanocomposite material NaM-AgI were studied,showing that the absorption bands of the diffuse reflectance absorption of the prepared material moved to the region of high energy.The absorption peak of the material prepared shifted to the region of high energy.Namely,blue shift was caused.This has demonstrated the incorporation of silver iodide into the channels of the zeolite.We observed the luminescence and surface photovoltage spectra of NaM-AgI sample,proposing the mechanisms of the photoluminescence and photovoltaic responses.

  16. Solvatochromic effect and kinetics of methyl violet reduction with potassium iodide in water-isopropanol mixtures

    Science.gov (United States)

    Ashfaq, Maria; Saeed, Rehana; Khan, Sameera Razi; Masood, Summyia

    2016-12-01

    The solvent influence on the reduction kinetics of methyl violet with iodide in binary mixture of aqueous isopropanol was investigated spectrophotometrically. The absorption spectra of methyl violet were recorded in water, aqueous isopropanol and absolute isopropanol. In these solvents λmax was in the range from 580.5 to 582.5 nm. The CNIBS/R-K model was used to calculate the solvatochromic parameters in a binary mixture; polynomial equation was also applied to describe the experimental data. The transition energies ( E T) were calculated. They show bathochromic shift with the decrease in the polarity of the solvent. The temperature was varied from 298-318 K, while the pH of the reaction was maintained at 4.99 and 6.00. The reduction reaction was found to be first order by potassium iodide and zero order by methyl violet. The thermodynamic parameters were also evaluated to support the kinetic data.

  17. Crystal structure of catena-poly[[potassium-tri-μ-dimethylacetamide-κ6O:O] iodide

    Directory of Open Access Journals (Sweden)

    Cezar-Catalin Comanescu

    2014-10-01

    Full Text Available The structure of catena-poly[[potassium-tri-μ-dimethylacetamide-κ6O:O] iodide], {[K(C4H9NO3]I}n, at 120 K has trigonal (P-3 symmetry. The structure adopts a linear chain motif parallel to the crystallographic c axis. Two crystallographically independent K+ cations are present in the asymmetric unit located on threefold rotoinversion axes at [0, 0, 0] and [0, 0, 1/2] and are bridged by the O atoms of the acetamide moiety. This is an example of a rare μ2-bridging mode for dimethylacetamide O atoms. The iodide counter-ion resides on a threefold rotation axis in the channel formed by the [K(C4H9NO]+ chains.

  18. Gastro-intestinal basidiobolomycosis in a 2-year-old boy: dramatic response to potassium iodide.

    Science.gov (United States)

    Sanaei Dashti, Anahita; Nasimfar, Amir; Hosseini Khorami, Hossein; Pouladfar, Gholamreza; Kadivar, Mohammad Rahim; Geramizadeh, Bita; Khalifeh, Masoomeh

    2016-07-04

    Gastro-intestinal basidiobolomycosis (GIB) is a rare fungal infection caused by Basidiobolus ranarum. Treatment includes surgical resection and long-term antifungal therapy. A 2.5-year-old boy presented with a 10-day history of abdominal pain, fever and diarrhoea, and a palpable abdominal mass was detected. Resection was undertaken and histology confirmed basidiobolomycosis. Treatment with amphotericin B and itraconazole was commenced, but the infection progressed and spread to involve the intestines, liver, ribs and lung, and also the abdominal wall after 6 months, requiring four operative procedures. Because of unresponsiveness to amphotericin and itraconazole, oral potassium iodide was added which resulted in complete resolution of the infection. Potassium iodide is an essential component of the treatment of systemic B. ranarum.

  19. Conclusion on the peer review of the pesticide risk assessment of the active substance potassium iodide

    Directory of Open Access Journals (Sweden)

    European Food Safety Authority

    2013-06-01

    Full Text Available The conclusions of the European Food Safety Authority (EFSA following the peer review of the initial risk assessments carried out by the competent authority of the rapporteur Member State the Netherlands, for the pesticide active substance potassium iodide are reported. The context of the peer review was that required by Commission Regulation (EU No 188/2011. The conclusions were reached on the basis of the evaluation of the representative uses of potassium iodide as a fungicide on tomatoes, sweet peppers, cucumber, eggplant, strawberries and ornamental flowers in greenhouse and field applications on strawberries. The reliable endpoints concluded as being appropriate for use in regulatory risk assessment, derived from the available studies and literature in the dossier peer reviewed, are presented. Missing information identified as being required by the regulatory framework is listed. Concerns are identified.

  20. Comparison of chlorine and chlorine dioxide toxicity of fathead minnows and bluegill

    Energy Technology Data Exchange (ETDEWEB)

    Wilde, E.W.; Soracco, R.J.; Mayack, L.A.; Shealy, R.L.; Broadwell, T.L.; Steffen, R.F.

    1983-01-01

    The comparative toxicity of total residual chlorine (TRC) and chlorine dioxide (ClO/sub 2/) was evaluated by conducting 96 h flow-through bioassays with three types of fish. The fish were subjected to an intermittent exposure regime in which biocide residuals were present for approximately 2-h periods beginning at 0, 24, 48 and 72 h into the tests. These conditions simulated the antifouling procedure (1 h day/sup -1/ biocide addition) used to control biofouling of nuclear reactor heat exchangers at the Savannah River Plant near Aiken, South Carolina. LC/sub 50/ values showed that ClO/sub 2/ was approximately 2 to 4 times more toxic than TRC to: (1) juvenile and 1-year-old fathead minnows (Pimphales promelas); and (2) young-of-the-year bluegill (Lepomis macrochirus). The TRC mean 96-h LC/sub 50/ values were: 0.08 mg l/sup -1/ for juvenile fathead minnows, 0.35 mg l/sup -1/ for adult fathead minnows and 0.44 mg l/sup -1/ for young-of-the-year bluegills. The ClO/sub 2/ mean LC/sub 50/ values were: 0.02 mg l/sup -1/ for juvenile fathead minnows, 0.17 mg l/sup -1/ for adult fathead minnows and 0.15 mg l/sup -1/ for young-of-the-year bluegills. 31 references, 1 figure, 3 tables.

  1. Chlorination of tramadol: Reaction kinetics, mechanism and genotoxicity evaluation.

    Science.gov (United States)

    Cheng, Hanyang; Song, Dean; Chang, Yangyang; Liu, Huijuan; Qu, Jiuhui

    2015-12-01

    Tramadol (TRA) is one of the most detected analgesics in environmental matrices, and it is of high significance to study the reactivity of TRA during chlorination considering its potential toxicity to the environment. The chlorine/TRA reaction is first order with respect to the TRA concentration, and a combination of first-order and second-order with respect to chlorine concentration. The pH dependence of the observed rate constants (kobs) showed that the TRA oxidation reactivity increased with increasing pH. kobs can be quantitatively described by considering all active species including Cl2, Cl2O and HOCl, and the individual rate constants of HOCl/TRA(0), HOCl/TRAH(+), Cl2/TRA and Cl2O/TRA reactions were calculated to be (2.61±0.29)×10(3)M(-1)s(-1), 14.73±4.17M(-1)s(-1), (3.93±0.34)×10(5)M(-1)s(-1) and (5.66±1.83)×10(6)M(-1)s(-1), respectively. Eleven degradation products were detected with UPLC-Q-TOF-MS, and the corresponding structures of eight products found under various pH conditions were proposed. The amine group was proposed to be the initial attack site under alkaline pH conditions, where reaction of the deprotonated amine group with HOCl is favorable. Under acidic and neutral pH conditions, however, two possible reaction pathways were proposed. One is an electrophilic substitution on the aromatic ring, and another is an electrophilic substitution on the nitrogen, leading to an N-chlorinated intermediate, which can be further oxidized. Finally, the SOS/umu test showed that the genotoxicity of TRA chlorination products increased with increasing dosage of chlorine, which was mostly attributed to the formation of some chlorine substitution products.

  2. CHLORINATION OF AMINO ACIDS: REACTION PATHWAYS AND REACTION RATES.

    Science.gov (United States)

    How, Zuo Tong; Linge, Kathryn; Busetti, Francesco; Joll, Cynthia A

    2017-03-15

    Chlorination of amino acids can result in the formation of organic monochloramines or organic dichloramines, depending on the chlorine to amino acid ratio (Cl:AA). After formation, organic chloramines degrade into aldehydes, nitriles and N-chloraldimines. In this paper, the formation of organic chloramines from chlorination of lysine, tyrosine and valine were investigated. Chlorination of tyrosine and lysine demonstrated that the presence of a reactive secondary group can increase the Cl:AA ratio required for the formation of N,N-dichloramines, and potentially alter the reaction pathways between chlorine and amino acids, resulting in the formation of unexpected by-products. In a detailed investigation, we report rate constants for all reactions in the chlorination of valine, for the first time, using experimental results and modelling. At Cl:AA = 2.8, the chlorine was found to first react quickly with valine (5.4x104 M-1 s-1) to form N-monochlorovaline, with a slower subsequent reaction with N-monochlorovaline to form N,N-dichlorovaline (4.9x102 M-1 s-1), although some N-monochlorovaline degraded into isobutyraldehyde (1.0x10-4 s-1). The N,N-dichlorovaline then competitively degraded into isobutyronitrile (1.3x10-4 s-1) and N-chloroisobutyraldimine (1.2x10-4 s-1). In conventional drinking water disinfection, N-chloroisobutyraldimine can potentially be formed in concentrations higher than its odour threshold concentration, resulting in aesthetic challenges and an unknown health risk.

  3. Nitro-Grela-type complexes containing iodides – robust and selective catalysts for olefin metathesis under challenging conditions

    Directory of Open Access Journals (Sweden)

    Andrzej Tracz

    2015-10-01

    Full Text Available Iodide-containing nitro-Grela-type catalysts have been synthesized and applied to ring closing metathesis (RCM and cross metathesis (CM reactions. These new catalysts have exhibited improved efficiency in the transformation of sterically, non-demanding alkenes. Additional steric hindrance in the vicinity of ruthenium related to the presence of iodides ensures enhanced catalyst stability. The benefits are most apparent under challenging conditions, such as very low reaction concentrations, protic solvents or with the occurrence of impurities.

  4. Nitro-Grela-type complexes containing iodides – robust and selective catalysts for olefin metathesis under challenging conditions

    Science.gov (United States)

    Tracz, Andrzej; Matczak, Mateusz; Urbaniak, Katarzyna

    2015-01-01

    Summary Iodide-containing nitro-Grela-type catalysts have been synthesized and applied to ring closing metathesis (RCM) and cross metathesis (CM) reactions. These new catalysts have exhibited improved efficiency in the transformation of sterically, non-demanding alkenes. Additional steric hindrance in the vicinity of ruthenium related to the presence of iodides ensures enhanced catalyst stability. The benefits are most apparent under challenging conditions, such as very low reaction concentrations, protic solvents or with the occurrence of impurities. PMID:26664602

  5. Nitro-Grela-type complexes containing iodides - robust and selective catalysts for olefin metathesis under challenging conditions.

    Science.gov (United States)

    Tracz, Andrzej; Matczak, Mateusz; Urbaniak, Katarzyna; Skowerski, Krzysztof

    2015-01-01

    Iodide-containing nitro-Grela-type catalysts have been synthesized and applied to ring closing metathesis (RCM) and cross metathesis (CM) reactions. These new catalysts have exhibited improved efficiency in the transformation of sterically, non-demanding alkenes. Additional steric hindrance in the vicinity of ruthenium related to the presence of iodides ensures enhanced catalyst stability. The benefits are most apparent under challenging conditions, such as very low reaction concentrations, protic solvents or with the occurrence of impurities.

  6. Development and testing of a silver chloride-impregnated activated carbon for aqueous removal and sequestration of iodide.

    Science.gov (United States)

    Karanfil, T; Moro, E C; Serkiz, S M

    2005-11-01

    Silver impregnated activated carbon (SIAC) can effectively remove iodide from water and sequester it in the form of AgI(s)). Given the extremely insoluble nature of AgI(s), the spent SIAC can be safely disposed of in land burial facilities. However, when the molar ratio of silver to iodide is greater than one, which is typical for waters contaminated with iodide, unreacted silver on the SIAC leached into solution with decreasing pH. To minimize silver leaching, a silver chloride impregnated activated carbon (SIAC-Cl) was produced from a SIAC. Scanning electron microscopy (SEM), energy-dispersive X-ray (EDX) and X-Ray Diffraction (XRD) analyses confirmed the presence of silver chloride on the SIAC-Cl. Batch isotherm experiments conducted at pH 5, 7 and 8 showed that the iodide uptakes of SIAC-Cl and SIAC were similar and independent of pH. SEM/EDX and XRD analyses after reaction with iodide indicated that chloride was exchanged with iodide to form AgI(s) on the SIAC-Cl. Batch leaching experiments demonstrated that leaching of silver from SIAC-Cl under acidic conditions was significantly lower than from SIAC. The performance of SIAC and SIAC-Cl for practical applications was evaluated by conducting column experiments using a radioactively contaminated groundwater that included 129I. SIAC and SIAC-Cl showed similar degrees of iodide uptake. However, a significant degree of silver leaching, about 50% of the total silver, occurred from the SIAC during the course of the column experiments, whereas silver leaching from SIAC-Cl was remarkably low (only 6% of the total silver). SIAC-Cl appears to be a suitable getter material to remove and sequester iodide from contaminated waste streams.

  7. Peroxide effects of iodide excess on mitochondria in Fischer rat thyroid cell line in the early period

    Institute of Scientific and Technical Information of China (English)

    李敏

    2014-01-01

    Objective To investigate the peroxide effects of iodide excess on mitochondria in Fischer rat thyroid cell line(FRTL)in the early period.Methods After treatment with 0.0 mmol/L(control group)or 0.1 mmol/L potassium iodide(KI)for 2,4 and 24 h,respectively,changes of mitochondrial superoxide formation were assayed by flow cytometry and fluorescence microscopy using mitochondria-targeted hydroethidine(Mito SOX).

  8. Effects of short-term potassium iodide treatment for thyrotoxicosis due to Graves disease in children and adolescents

    OpenAIRE

    Jeong, Kyung Uk; Lee, Hae Sang; Hwang, Jin Soon

    2014-01-01

    Purpose Graves disease is the most common cause of hyperthyroidism in children. Inorganic iodide has been used in combination with antithyroid drugs for more effective normalization of thyroid hormones in some cases of severe thyrotoxicosis. This study aimed to investigate clinical characteristics of childhood thyrotoxicosis and effectiveness of inorganic iodide in the early phase of treatment. Methods Sixty-seven pediatric patients (53 girls/14 boys, 11.1±3.4 years of age), with newly diagno...

  9. Study on Growth and Optical, Scintillation Properties of Thallium Doped Cesium Iodide –Scintillator Crystal

    Directory of Open Access Journals (Sweden)

    B. Ravi

    2014-06-01

    Full Text Available Single crystal of Thallium doped cesium Iodide –Scintillator crystal was grown using vertical Bridgeman technique. The grown crystal was included for cutting and polishing for the characterization purpose and this crystal was studied by optical transmission properties, photo luminescence and thermally luminescence characteristics. Gamma-ray detectors were fabricated using the grown crystal that showed good linearity and nearly 7.5% resolution at 662 keV.

  10. Rationale for the real-time and dynamic cell death assays using propidium iodide

    OpenAIRE

    Zhao, Hong; Oczos, Jadwiga; Janowski, Pawel; Trembecka, Dominika; Dobrucki, Jurek; Darzynkiewicz, Zbigniew; Wlodkowic, Donald

    2010-01-01

    We have recently reported an innovative approach to use charged fluorochromes such as propidium iodide (PI) in the real-time, dynamic cell viability assays. The present study was designed to provide a mechanistic rationale for the kinetic assays using cell permeability markers. Uptake of PI by live cells, effect on the cell cycle, long term proliferation capacity, DNA damage response and pharmacologic interactions with anticancer drugs were studied using both laser scanning microscopy and las...

  11. Studies on the Mechanisms of Methyl Iodide Adsorption and Iodine Retention on Silver-Mordenite

    Energy Technology Data Exchange (ETDEWEB)

    Nenoff, Tina Maria [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Soelberg, Nick [Idaho National Lab. (INL), Idaho Falls, ID (United States)

    2014-09-01

    Silver-containing mordenite (MOR) is a longstanding benchmark for radioiodine capture, reacting with molecular iodine (I2) to form AgI. However the mechanisms for organoiodine capture are not well understood. Here we investigate the capture of methyl iodide from complex mixed gas streams by combining chemical analysis of the effluent gas stream with in depth characterization of the recovered sorbent.

  12. Study on the Preparation and Characteristics of Cellulose/Silver Iodide Nanocomposite Film.

    Science.gov (United States)

    Lee, Yang Hun; Han, Sung Soo; Kang, Young Ah; Shin, Eun Joo

    2016-06-01

    In this study, the structure and properties of an organic-inorganic composite material prepared from cellulose doped with fine particles of silver iodide (AgI) were examined. The preparation of the composite involved the complexation of cellulose with polyiodide ions, such as I- and 13-, by immersion in iodine/potassium iodide (I2/KI: 0.2, 0.4, 0.6, 0.8, 1.0 M) or potassium iodide (KI: 0.6, 1.2, 1.8, 2.4, 3.0 M) aqueous solutions followed by reaction in a silver nitrate (AgNO3:1.0 M) aqueous solution. These procedures resulted in the in situ formation of fine β-AgI particles within the cellulose matrix. The characteristics and conductivities of prepared cellulose/silver iodide (AgI) nanocomposite films with different I2/KI and KI concentrations were investigated. AgI particle formation and aggregation increased on increasing I2/KI and KI concentrations as determined by SEM. X-ray results showed that KI could penetrate the cellulose crystal region and form AgI particles. The electrical conductivities of nanocomposite films treated with KI were higher than that of I2/KI at < 1.0 M of I2/KI and 3 M of KI, although the weight gain by AgI formation was lower than that of I2/KI. This was also attributed to the formation of smaller AgI particles and crystal defects. Highest electrical conductivity (3.8 x 10(-7) Ω(-1) cm(-1)) was obtained from the cellulose films (1.25 x 10(-11) Ω(-1) cm(-1)) treated with the aqueous solutions of 1.0 M I2/KI and 1.0 M AgNO3.

  13. Electrochemical reduction characteristics and the mechanism of chlorinated hydrocarbons at the copper electrode

    Institute of Scientific and Technical Information of China (English)

    XU Wenying; GAO Tingyao; ZHOU Rongfeng; MA Lumin

    2007-01-01

    The electrochemical reduction characteristies of chlorinated hyrdrocarbons were investigated by cyclic voltammetry technique.The reduction mechanism and activity of the chlorinated hydrocarbons at the copper electrode were explored.The relationship between the structure of chlorinated hydrocarbons and their reductive activity were discussed.The experimental results showed that chlorinated alkanes and a portion of chlorinated aromatic hydrocarbons could be reduced directly at the copper electrode.However,chlorinated aromatic hydrocarbons were not easy to reduce at the copper electrode.The results provided a theoretical basis for the catalyzed iron inner electrolysis method.

  14. Study on metal corrosion caused by chlorine dioxide of various purities

    Institute of Scientific and Technical Information of China (English)

    崔崇威; 黄君礼; 许晶

    2004-01-01

    Weight lost method was used to comparatively study the corrosion behavior of four different metals under the dosage of chlorine dioxide, chlorine and their mixture respectively. The experimental results indicated that chlorine causes the most serious corrosion of carbon steel, and the higher the concentration of chlorine, the more serious the corrosion. On the contras, metals corrosion is the least serious in the case of chlorine dioxide.The results further revealed that chlorine dioxide is the most effective water treatment reagent, making it the best choice to use extensively in circulated cooling water disinfection and corrosion control.

  15. Radiofrequency induction on sodium/iodide symporter expression of thyroid cancer

    Institute of Scientific and Technical Information of China (English)

    Youxin Tian; Qinjiang Liu; Yaqiong Ni

    2013-01-01

    Objective:The aim of this study was to investigate the ef ects of radiofrequency treatment on sodium/iodide symporter expression of thyroid cancer cells. Methods:In 29 thyroid cancer patients with low or no expression of soda\\iodide symporter, the radio frequency combined 131I therapy was used, the whole-body scintigraphy and serum Ig were detected before and after the radiofrequency treatment. Results:The whole-body scintigraphy showed that 4 cases (4/29) before radiofrequency treatment had positive iodine uptake, 19 cases (19/29) two weeks after radiofrequency treatment had the positive iodine uptake, 12 cases (12/29) four weeks after radiofrequency treatment had the positive iodine uptake. Four weeks after radiofrequency treatment, 5 cases had increased serum Ig levels, 17 cases had decreased serum Ig levels, 7 cases showed no change. 25 cases (25/29) were ef ective, 15 cases (15/29) were cured. Conclusion:The radiofrequency induced the non-expressed the sodium/iodide symporter of thyroid cancer cells regain the iodine intake ability, it improved the clinical ef icacy of 131I therapy in dedif erentiated thyroid cancer.

  16. Deteksi Natrium/Iodide Symporter (NIS pada Galur Sel Kanker Payudara SKBR3 dengan Imunositofluoresens

    Directory of Open Access Journals (Sweden)

    Aisyah Elliyanti

    2016-03-01

    Full Text Available SKBR-3 cell line is a breast cancer model for human epidermal growth factor receptor2 (HER2 positive. Only 50% of patients of this type have fully responded to chemotherapy. Natrium iodide symporter expression correlates with the uptake and ability of cells to accumulate radioiodine. The aim of this study was to examine natrium/iodide symporter (NIS expression and its distribution with and without epidermal growth factor (EGF treatment using immunocytofluoresence (ICF. This study was conducted at the Cell Culture Laboratory, Faculty of Medicine, Universitas Padjadjaran from September 2013 to April 2014. SKBR3 cells were cultured until 70% confluent. Cells were then divided into two groups: treatment group and control group. The treatment group was treated with EGF 50 ng/mL. Cells were incubated with primary antibody rabbit polyclonal antibody anti-NIS, and then were followed with secondary-antibody goat polyclonal antibody to rabbit. Data from the observation were then assessed semi-quantitatively. Natrium/iodide symporter was seen to be expressed and distributed in the cytoplasm. Cells induced by EGF showed significant increase in NIS expression in cytoplasm and its distribution in cell membrane. It is concluded that the SKBR3 cells express NIS in cytoplasm and that EGF induction increases NIS expression and distribution in cell membrane. This finding leads to a potential ability of breast cancer cells to uptake and accumulate radioiodine.

  17. Uptake of iodide by a mixture of metallic copper and cupric compounds

    Energy Technology Data Exchange (ETDEWEB)

    Lefevre, G.; Alnot, M.; Ehrhardt, J.J.; Bessiere, J. [Univ. Henri Poincare Nancy 1, Villers les Nancy (France). Lab. de Chimie Physique pour l`Environnement

    1999-05-15

    Environmental contaminants harmful to the health of present and future generations involve nuclear fission products as iodine radioisotopes. {sup 129}I is potentially one of the more mobile products because of its long half-life and its tendency to go into solution as an anion that is not retarded with silicate minerals. Ability of copper/cupric compound mixtures to remove iodide from solution was investigated to predict sorption of radioactive iodine in the environment and to assess their use in a nuclear reprocessing method. Thermodynamic calculations were performed to study the stability of such mixtures in solution and to obtain equilibrium constants of Cu(0)/Cu(II)/I{sup {minus}} and Cu(0)/Cu(II)/Cl{sup {minus}} systems. Both calculations and experimental results showed that a Cu(0)/Cu{sub 3}(OH){sub 2}(CO{sub 3}){sub 2} (azurite) mixture selectively uptakes iodide ions (initial concentrations: 10{sup {minus}2} and 10{sup {minus}1} M) in the presence of 10{sup {minus}1} M chloride ions. Reaction of iodide with copper powder and azurite crystal or copper plate and azurite powder have also been investigated, leading to precipitation of CuI onto massive copper phase. The different solids were separately analyzed by XPS and MEB-EDX, giving some insight in the uptake mechanism. It is proposed that soluble copper released by the cupric compound is reduced at the surface of metallic copper, leading to a preferential precipitation of CuI on copper surface.

  18. Use of potassium iodide in dermatology: updates on an old drug.

    Science.gov (United States)

    Costa, Rosane Orofino; Macedo, Priscila Marques de; Carvalhal, Aline; Bernardes-Engemann, Andréa Reis

    2013-01-01

    Potassium iodide, as a saturated solution, is a valuable drug in the dermatologist's therapeutic arsenal and is useful for the treatment of different diseases due to its immunomodulatory features. However, its prescription has become increasingly less frequent in dermatology practice. Little knowledge about its exact mechanism of action, lack of interest from the pharmaceutical industry, the advent of new drugs, and the toxicity caused by the use of high doses of the drug are some possible explanations for that. Consequently, there are few scientific studies on the pharmacological aspects, dosage and efficacy of this drug. Also, there is no conventional standard on how to manipulate and prescribe the saturated solution of potassium iodide, which leads to unawareness of the exact amount of the salt being delivered in grams to patients. Considering that dosage is directly related to toxicity and the immunomodulatory features of this drug, it is essential to define the amount to be prescribed and to reduce it to a minimum effective dose in order to minimize the risks of intolerance and thus improve treatment adherence. This review is relevant due to the fact that the saturated solution of potassium iodide is often the only therapeutic choice available for the treatment of some infectious, inflammatory and immune-mediated dermatoses, no matter whether the reason is specific indication, failure of a previous therapy or cost-effectiveness.

  19. Simple and rapid determination of iodide in table salt by stripping potentiometry at a carbon-paste electrode.

    Science.gov (United States)

    Svancara, Ivan; Ogorevc, Bozidar; Nović, Milko; Vytras, Karel

    2002-04-01

    A simple and rapid procedure, utilising constant-current stripping analysis (CCSA) at a carbon-paste electrode containing tricresyl phosphate as a pasting liquid (TCP-CPE), has been developed for the determination of iodide in table salt. Because of a synergistic accumulation mechanism based on ion-pairing and extraction of iodide in combination with electrolytic pretreatment of the TCP-CPE, the method is selective for iodide and enables direct determination of iodide in samples of table salt containing anti-caking agents such as K(4)[Fe(CN)(6)] (food additive "E 536") or MgO. The iodide content (calculated as KI) can be determined in a concentration range of 2 to 100 mg kg(-1) salt, with a detection limit (S/N=3) of 1 mg kg(-1), and a recovery from 90 to 115%. The proposed method has been used to determine iodide in several types of artificially iodised table salt and in one sample of natural sea salt. The results obtained agreed well with those obtained by use of three independent reference methods (titration, spectrophotometry, and ICP-MS) used to validate the CCSA method, indicating that the developed method is applicable as a routine procedure for rapid testing in salt production process control and in the analysis of marketed table salts.

  20. Activation of the Nrf2-Keap 1 Pathway in Short-Term Iodide Excess in Thyroid in Rats

    Directory of Open Access Journals (Sweden)

    Tingting Wang

    2017-01-01

    Full Text Available Wistar rats were randomly divided into groups of varying iodide intake: normal iodide; 10 times high iodide; and 100 times high iodide on Days 7, 14, and 28. Insignificant changes were observed in thyroid hormone levels (p>0.05. Urinary iodine concentration and iodine content in the thyroid glands increased after high consumption of iodide from NI to 100 HI (p<0.05. The urinary iodine concentration of the 100 HI group on Days 7, 14, and 28 was 60–80 times that of the NI group. The mitochondrial superoxide production and expressions of Nrf2, Srx, and Prx 3 all significantly increased, while Keap 1 significantly decreased in the 100 HI group when compared to the NI or 10 HI group on Days 7, 14, and 28 (p<0.05. Immunofluorescence staining results showed that Nrf2 was localized in the cytoplasm in NI group. Although Nrf2 was detected in both cytoplasm and nucleus in 10 HI and 100 HI groups, a stronger positive staining was found in the nucleus. We conclude that the activation of the Nrf2-Keap 1 antioxidative defense mechanism may play a crucial role in protecting thyroid function from short-term iodide excess in rats.

  1. Activation of the Nrf2-Keap 1 Pathway in Short-Term Iodide Excess in Thyroid in Rats

    Science.gov (United States)

    Liang, Xue

    2017-01-01

    Wistar rats were randomly divided into groups of varying iodide intake: normal iodide; 10 times high iodide; and 100 times high iodide on Days 7, 14, and 28. Insignificant changes were observed in thyroid hormone levels (p > 0.05). Urinary iodine concentration and iodine content in the thyroid glands increased after high consumption of iodide from NI to 100 HI (p Prx 3 all significantly increased, while Keap 1 significantly decreased in the 100 HI group when compared to the NI or 10 HI group on Days 7, 14, and 28 (p < 0.05). Immunofluorescence staining results showed that Nrf2 was localized in the cytoplasm in NI group. Although Nrf2 was detected in both cytoplasm and nucleus in 10 HI and 100 HI groups, a stronger positive staining was found in the nucleus. We conclude that the activation of the Nrf2-Keap 1 antioxidative defense mechanism may play a crucial role in protecting thyroid function from short-term iodide excess in rats. PMID:28133506

  2. Chlorine solubility in evolved alkaline magmas

    Directory of Open Access Journals (Sweden)

    M. R. Carroll

    2005-06-01

    Full Text Available Experimental studies of Cl solubility in trachytic to phonolitic melts provide insights into the capacity of alkaline magmas to transport Cl from depth to the earth?s surface and atmosphere, and information on Cl solubility variations with pressure, temperature and melt or fluid composition is crucial for understanding the reasons for variations in Cl emissions at active volcanoes. This paper provides a brief review of Cl solubility experiments conducted on a range of trachytic to phonolitic melt compositions. Depending on the experimental conditions the melts studied were in equilibrium with either a Cl-bearing aqueous fluid or a subcritical assemblage of low- Cl aqueous fluid + Cl-rich brine. The nature of the fluid phase(s was identified by examination of fluid inclusions present in run product glasses and the fluid bulk composition was calculated by mass balance. Chlorine concentrations in the glass increase with increasing Cl molality in the fluid phase until a plateau in Cl concentration is reached when melt coexists with aqueous fluid + brine. With fluids of similar Cl molality, higher Cl concentrations are observed in peralkaline phonolitic melts compared with peraluminous phonolitic melts; overall the Cl concentrations observed in phonolitic and trachytic melts are approximately twice those found in calcalkaline rhyolitic melts under similar conditions. The observed negative pressure dependence of Cl solubility implies that Cl contents of melts may actually increase during magma decompression if the magma coexists with aqueous fluid and Cl-rich brine (assuming melt-vapor equilibrium is maintained. The high Cl contents (approaching 1 wt% Cl observed in some melts/glasses from the Vesuvius and Campi Flegrei areas suggest saturation with a Cl-rich brine prior to eruption.

  3. Inactivation of antibiotic resistance genes in municipal wastewater effluent by chlorination and sequential UV/chlorination disinfection.

    Science.gov (United States)

    Zhang, Yingying; Zhuang, Yao; Geng, Jinju; Ren, Hongqiang; Zhang, Yan; Ding, Lili; Xu, Ke

    2015-04-15

    This study investigated disinfection methods including chlorination, ultraviolet (UV) irradiation and sequential UV/chlorination treatment on the inactivation of antibiotic resistance genes (ARGs). ARGs including sul1, tetX, tetG, intI1, and 16S rRNA genes in municipal wastewater treatment plant (MWTP) effluent were examined. The results indicated a positive correlation between the removal of ARGs and chlorine dosage (p=0.007-0.014, n=6),as well as contact time (p=0.0001, n=10). Greater free chlorine (FC) dosage leads to higher removal for all the genes and the maximum removal (1.30-1.49 logs) could be achieved at FC dosage of 30 mg L(-1). The transformation kinetic data for ARGs removal (log C0/C) followed the second-order reaction kinetic model with FC dosage (R(2)=0.6829-0.9999) and contact time (R(2)=0.7353-8634), respectively. Higher ammonia nitrogen (NH3-N) concentration was found to lead to lower removal of ARGs at the same chlorine dosage. When the applied Cl2:NH3-N ratio was over 7.6:1, a significant reduction of ARGs (1.20-1.49 logs) was achieved. By using single UV irradiation, the log removal values of tetX and 16Ss rRNA genes were 0.58 and 0.60, respectively, while other genes were 0.36-0.40 at a fluence of 249.5 mJ cm(-2), which was observed to be less effective than chlorination. With sequential UV/chlorination treatment, 0.006 to 0.31 log synergy values of target genes were observed under different operation parameters.

  4. Rapid Determination of HAAs Formation Potential of the Reaction of Humic Acid with Chlorine or Chlorine Dioxide

    Institute of Scientific and Technical Information of China (English)

    ZHU Zhi-liang; GE Yuan-xin; ZHANG Rong-hua; MA Hong-mei; HAO Jian-fu

    2007-01-01

    On the basis of gas chromatography(GC) coupled with a short capillary column and an electron capture detector(ECD), a simple and rapid method for the determination of five haloacetic acids(HAAs) in drinking water was developed by the optimization of derivation conditions and the modification of gas chromatographic program. HAAs formation potential(HAAFP) of the reaction of humic acid with chlorine was determined via this method. The major advantages of the method are the simplicity of chromatographic temperature program and the short run time of GC. Dichloroacetic acid(DCAA) and Trichloroacetic acid(TCAA), which were detected in the determination of HAAFP, were rapidly formed in the first 72 h of the reaction of humic acid with chlorine. HAAFP of the reaction of humic acid with chlorine increased with the increase in the concentrations of humic acid and chlorine. The average HAAFP of the reaction of humic acid with chlorine was 39.9 μg/mg TOC under the experimental conditions. When the concentration of humic acid was 4 mg/L, the concentration of HAAs, which were produced in the reaction of humic acid with chorine, may exceed MCL of 60 μg/L HAAs as the water quality standards for urban water supply of China and the first stage of US EPA disinfection/disinfection by-products(D/DBP) rule; when the concentration of humic acid was 2 mg/L, the concentration of HAAs may exceed MCL of 30 μg/L HAAs for the second stage of US EPA D/DBP rule. When humic acid was reacted with chlorine dioxide, only DCAA was detected with a maximum concentration of 3.3 μg/L at a humic acid content of 6 mg/L. It was demonstrated that the substitution of chlorine dioxide for chorine may entirely or partly control the formation of HAAs and effectively reduce the health risk associated with disinfected drinking water.

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

    Energy Technology Data Exchange (ETDEWEB)

    Fontcuberta, M. [Agencia de Salut Publica de Barcelona, ASPB, Public Health Agency of Barcelona, Av Drassanes 13, 08001 Barcelona (Spain)], E-mail: mfontcub@aspb.es; Arques, J.F.; Villalbi, J.R.; Martinez, M.; Centrich, F.; Serrahima, E.; Pineda, L.; Duran, J.; Casas, C. [Agencia de Salut Publica de Barcelona, ASPB, Public Health Agency of Barcelona, Av Drassanes 13, 08001 Barcelona (Spain)

    2008-01-15

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

  6. Intra- and intermembrane distribution of chlorin e6 derivatives

    Science.gov (United States)

    Zorin, Vladimir P.; Zorina, Tatyana E.; Mikhalovsky, Iosif S.; Khludeyev, Ivan I.

    1995-01-01

    The parameters of chlorin e6 and trimethylester of chlorin e6 incorporation and distribution in suspensions of unilamellar liposomes of DMPC, DPPC, and DSPC, as well as efficiency of the pigment redistribution from liposomes to cellular membranes have been studied. Determination of the fraction of pigments' fluorescence which is accessible to quenching by a watersoluble quencher indicates that for both chlorins the outer monolayer of the liposomal membrane is more populated than the inner one. Gel-liquid crystalline phase transition induces a shift of a part of the pigments' molecules toward the inner monolayer. By means of ultrafiltration technique it is shown that chlorins binding to liposomal membrane occurs as partitioning between water and lipid phases. The partition coefficient is affected strongly by the type of pigment, the phase state of the lipid bilayer. Similar results were obtained when the influence of the physical state of the lipid bilayer on the rate of chlorins redistribution from liposomes to cellular membrane was studied. These findings show that diffusive mobility of the sensitizer in suspensions of cellular and model membranes is a complex process which is dependent on structural features of both the pigment and its biological carriers.

  7. Synthesis of magnesium aluminate spinel by periclase and alumina chlorination

    Energy Technology Data Exchange (ETDEWEB)

    Orosco, Pablo, E-mail: porosco@unsl.edu.ar [Instituto de Investigaciones en Tecnología Química (INTEQUI), Chacabuco y Pedernera, San Luis (Argentina); Facultad de Química, Bioquímica y Farmacia, Universidad Nacional de San Luis Chacabuco y Pedernera, San Luis (Argentina); Barbosa, Lucía [Instituto de Investigaciones en Tecnología Química (INTEQUI), Chacabuco y Pedernera, San Luis (Argentina); Instituto de Ciencias Básicas (ICB), Universidad Nacional de Cuyo Parque General San Martín, Mendoza (Argentina); Ruiz, María del Carmen [Instituto de Investigaciones en Tecnología Química (INTEQUI), Chacabuco y Pedernera, San Luis (Argentina); Facultad de Química, Bioquímica y Farmacia, Universidad Nacional de San Luis Chacabuco y Pedernera, San Luis (Argentina)

    2014-11-15

    Highlights: • Use of chlorination for the synthesis of magnesium aluminate spinel. • The reagents used were alumina, periclase and chlorine. • Isothermal and non-isothermal assays were performed in air and Cl{sub 2}–N{sub 2} flows. • The chlorination produced magnesium aluminate spinel at 700 °C. • Selectivity of the chlorination reaction to obtain spinel is very high. - Abstract: A pyrometallurgical route for the synthesis of magnesium aluminate spinel by thermal treatment of a mechanical mixture containing 29 wt% MgO (periclase) and 71 wt% Al{sub 2}O{sub 3} (alumina) in chlorine atmosphere was developed and the results were compared with those obtained by calcining the same mixture of oxides in air atmosphere. Isothermal and non-isothermal assays were performed in an experimental piece of equipment adapted to work in corrosive atmospheres. Both reagents and products were analyzed by differential thermal analysis (DTA), X-ray diffraction (XRD) and X-ray fluorescence (XRF). Thermal treatment in Cl{sub 2} atmosphere of the MgO–Al{sub 2}O{sub 3} mixture produces magnesium aluminate spinel at 700 °C, while in air, magnesium spinel is generated at 930 °C. The synthesis reaction of magnesium aluminate spinel was complete at 800 °C.

  8. Coagulation properties of anelectrochemically prepared polyaluminum chloride containing active chlorine

    Institute of Scientific and Technical Information of China (English)

    HU Chengzhi; LIU Huijuan; QU Jiuhui

    2006-01-01

    With high content of the Al13 species and the active chloride, an electrochemically prepared polyaluminum chloride (E-PACl) presents integrated efficiency of coagulation and oxidation. The coagulation properties of E-PACl were systemically investigated through jar tests in the various water quality conditions. The active chlorine in E-PACl can significantly influence the coagulation behavior due to the active chlorine preoxidation, which can change the surface charge characteristic of organic matter (OM) in water. The active chlorine preoxidation could improve the E-PACl coagulation efficiency if the water possessed the characteristics of relatively low OM content (2 mg/L) and high hardness (278 mg CaCO3/L). In the water with medium content of OM (5 mg/L), dosage would be a crucial factor to decide whether the active chlorine in E-PACl aided coagulation process or not. Comparing with alkaline condition, active chlorine would show a more significant influence on the coagulation process in acidic region.

  9. Transgenic plants and associated bacteria for phytoremediation of chlorinated compounds.

    Science.gov (United States)

    Van Aken, Benoit; Doty, Sharon Lafferty

    2010-01-01

    Phytoremediation is the use of plants for the treatment of environmental pollution, including chlorinated organics. Although conceptually very attractive, removal and biodegradation of chlorinated pollutants by plants is a rather slow and inefficient process resulting in incomplete treatment and potential release of toxic metabolites into the environment. In order to overcome inherent limitations of plant metabolic capabilities, plants have been genetically modified, following a strategy similar to the development of transgenic crops: genes from bacteria, fungi, and mammals involved in the metabolism of organic contaminants, such as cytochrome P-450 and glutathione S-transferase, have been introduced into higher plants, resulting in significant improvement of tolerance, removal, and degradation of pollutants. Recently, plant-associated bacteria have been recognized playing a significant role in phytoremediation, leading to the development of genetically modified rhizospheric and endophytic bacteria with improved biodegradation capabilities. Transgenic plants and associated bacteria constitute a new generation of genetically modified organisms for efficient and environmental-friendly treatment of polluted soil and water. This review focuses on recent advances in the development of transgenic plants and bacteria for the treatment of chlorinated pollutants, including chlorinated solvents, polychlorinated phenols, and chlorinated herbicides.

  10. Application of chlorine dioxide as an oilfield facilities treatment fluid

    Energy Technology Data Exchange (ETDEWEB)

    Romaine, J.; Strawser, T.G.; Knippers, M.L.

    1995-11-01

    Both mechanical and chemical treatments are used to clean water flood injection distribution systems whose efficiency has been reduced as a result of plugging material such as iron sulfide sludge. Most mechanical treatments rely on uniform line diameter to be effective, while chemical treatments require good contact with the plugging material for efficient removal. This paper describes the design and operation of a new innovative application using chlorine dioxide for the removal of iron sulfide sludge from water flood injection distribution systems. This technology has evolved from the use of chlorine dioxide in well stimulation applications. The use of chlorine dioxide for continuous treatment of injection brines will also be discussed. Exxon USA`s Hartzog Draw facility in Gillette, Wyoming was the site for the application described. 4,500 barrels of chlorine dioxide was pumped in three phases to clean sixty-six miles of the water flood distribution system. Results indicate that chlorine dioxide was effective in cleaning the well guard screens, the injection lines, frac tanks used to collect the treatment fluids and the injection wells.

  11. MECHANISM OF CHLORATE FORMATION IN CHLORINE DIOIXDE DELIGNIFICATION

    Institute of Scientific and Technical Information of China (English)

    Byung-Ho Yoon; Li-Jun Wang; Se-Jong Kim

    2004-01-01

    The effect of pH on chlorate formation during chlorine dioxide delignification of oxygen delignified kraft pulp was studied. Chlorate formation was found to increase slightly when pH was increased from 1.8 to 2.5, further increase of pH decreased chlorate formation.The above phenomenon is explained by the combination of two mechanisms, one by the reaction between hypochlorous acid and chlorite, another by the effect of chlorine on the regeneration of chlorine dioxide. The first mechanism suggests that chlorate formation is highly dependent on HCIO concentration which decreases with increasing pH and causes chlorate formation to behave in the same trend. The second mechanism suggests that chlorine favors the regeneration of chlorine dioxide while HCIO favors chlorate formation, thus lowering the pH from about 4 to the acidic end should decreases chlorate formation. The two opposite effects lead to the maximum formation of chlorate at around pH 2.5.

  12. Biofouling control: Bacterial quorum quenching versus chlorination in membrane bioreactors.

    Science.gov (United States)

    Weerasekara, Nuwan A; Choo, Kwang-Ho; Lee, Chung-Hak

    2016-10-15

    Biofilm formation (biofouling) induced via cell-to-cell communication (quorum sensing) causes problems in membrane filtration processes. Chorine is one of the most common chemicals used to interfere with biofouling; however, biofouling control is challenging because it is a natural process. This study demonstrates biofouling control for submerged hollow fiber membranes in membrane bioreactors by means of bacterial quorum quenching (QQ) using Rhodococcus sp. BH4 with chemically enhanced backwashing. This is the first trial to bring QQ alongside chlorine injection into practice. A high chlorine dose (100 mg/L as Cl2) to the system is insufficient for preventing biofouling, but addition of the QQ bacterium is effective for disrupting biofouling that cannot be achieved by chlorination alone. QQ reduces the biologically induced metal precipitate and extracellular biopolymer levels in the biofilm, and biofouling is significantly delayed when QQ is applied in addition to chlorine dosing. QQ with chlorine injection gives synergistic effects on reducing physically and chemically reversible fouling resistances while saving substantial filtration energy. Manipulating microbial community functions with chemical treatment is an attractive tool for biofilm dispersal in membrane bioreactors.

  13. Chlorination byproducts, their toxicodynamics and removal from drinking water.

    Science.gov (United States)

    Gopal, Krishna; Tripathy, Sushree Swarupa; Bersillon, Jean Luc; Dubey, Shashi Prabha

    2007-02-01

    No doubt that chlorination has been successfully used for the control of water borne infections diseases for more than a century. However identification of chlorination byproducts (CBPs) and incidences of potential health hazards created a major issue on the balancing of the toxicodynamics of the chemical species and risk from pathogenic microbes in the supply of drinking water. There have been epidemiological evidences of close relationship between its exposure and adverse outcomes particularly the cancers of vital organs in human beings. Halogenated trihalomethanes (THMs) and haloacetic acids (HAAs) are two major classes of disinfection byproducts (DBPs) commonly found in waters disinfected with chlorine. The total concentration of trihalomethanes and the formation of individual THM species in chlorinated water strongly depend on the composition of the raw water, on operational parameters and on the occurrence of residual chlorine in the distribution system. Attempts have been made to develop predictive models to establish the production and kinetics of THM formations. These models may be useful for operational purposes during water treatment and water quality management. It is also suggested to explore some biomarkers for determination of DBP production. Various methods have been suggested which include adsorption on activated carbons, coagulation with polymer, alum, lime or iron, sulfates, ion exchange and membrane process for the removal of DBPs. Thus in order to reduce the public health risk from these toxic compounds regulation must be inforced for the implementation of guideline values to lower the allowable concentrations or exposure.

  14. Inactivation of Aspergillus flavus in drinking water after treatment with UV irradiation followed by chlorination

    Energy Technology Data Exchange (ETDEWEB)

    Al-Gabr, Hamid Mohammad [Key Laboratory of Urban Environment and Health, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 361021 (China); State Key Laboratory of Environmental Sciences, and Key Laboratory of Ministry of Education for Coast and Wetland Ecosystems, School of Life Sciences, Xiamen University, Xiamen 361005 (China); Zheng, Tianling [State Key Laboratory of Environmental Sciences, and Key Laboratory of Ministry of Education for Coast and Wetland Ecosystems, School of Life Sciences, Xiamen University, Xiamen 361005 (China); Yu, Xin, E-mail: xyu@iue.ac.cn [Key Laboratory of Urban Environment and Health, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 361021 (China)

    2013-10-01

    The disinfection process for inactivating microorganisms at drinking water treatment plants is aimed for safety of drinking water for humans from a microorganism, such as bacteria, viruses, algae, fungi by using chlorination, ozonation, UV irradiation, etc. In the present study, a combination of two disinfectants, UV irradiation followed by chlorination, was evaluated for inactivating Aspergillus flavus under low contact time and low dosage of UV irradiation. The results indicated an inverse correlation between the inactivation of A. flavus by using UV irradiation only or chlorination alone. By using UV radiation, the 2 log{sub 10} control of A. flavus was achieved after 30 s of irradiation, while chlorination was observed to be more effective than UV, where the 2 log was achieved at chlorine concentration of 0.5, 1, 2 and 3 mg/l, in contact time of 60, 5, 1 and 1 min, respectively. However, combined use (UV irradiation followed by chlorination) was more effective than using either UV or chlorination alone; 5 s UV irradiation followed by chlorination produced 4 log{sub 10} reduction of A. flavus at chlorine concentrations of 2 and 3 mg/l under a contact time of 15 min. The results indicated that efficiency of UV irradiation improves when followed by chlorination at low concentrations. - Highlights: • As a disinfectant, chlorine is more effective than UV in inactivating Aspergillus flavus. • As a combined method, UV irradiation followed by chlorination shows high efficiency. • UV irradiation can improve effectiveness of chlorination in reducing Aspergillus flavus.

  15. Transformation of cefazolin during chlorination process: Products, mechanism and genotoxicity assessment

    Energy Technology Data Exchange (ETDEWEB)

    Li, Liping, E-mail: lisaleercees807@yahoo.cn; Wei, Dongbin, E-mail: weidb@rcees.ac.cn; Wei, Guohua, E-mail: wgh@rcees.ac.cn; Du, Yuguo, E-mail: duyuguo@rcees.ac.cn

    2013-11-15

    Highlights: • Base-catalyzed electrophilic substitution occurred in cefazolin chlorination. • Oxidation of thioether in cefazolin was found in chlorination process. • The pH conditions impacted on the occurrence of reaction types. • Genotoxicity had an elevation after chlorination of cefazolin. • Reaction pathways of cefazolin chlorination were replayed in surface water matrix. -- Abstract: Large quantities of cephalosporins have entered into aquatic environment in recent years, posing potential adverse effect to human health and ecological safety. In this study, cefazolin, one of widely used cephalosporins, was targeted to explore its transformation behaviors in chlorination disinfection process. With the help of ultra high performance liquid chromatography and high resolution mass spectroscopy, one chlorinated product and four oxidation products were detected in cefazolin chlorination system. The corresponding transformation pathways of cefazolin were proposed. Two kinds of reactions occurred in chlorination system, one was oxidation of thioether-sulfur to sulfoxide and di-sulfoxide, and the other was base-catalyzed electrophilic substitution of alpha-H of amide by chlorine atom. The pH value determined the occurrence of reaction types, and increasing chlorine dose promoted transformation of cefazolin. More importantly, genotoxicity in SOS/umu assay had an elevation after chlorination, which might be attributed to the formation of chlorinated product and sulfoxide during chlorination process.

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

    DEFF Research Database (Denmark)

    Damgaard, Ida

    Chlorinated solvents are among the most frequently found contaminants in groundwater. In fractured media, chlorinated ethenes and ethanes are transported downwards through preferential pathways with subsequent diffusion into the sediment matrix. Due to slow back diffusion it can serve as a long...... term secondary source that can leach to the underlying aquifer. As some of the chlorinated solvents and their degradation products are toxic and carcinogenic, remediation technologies applicable in low permeability settings are needed. Enhanced reductive dechlorination (ERD) has been proven efficient...... and ethanes in clay till (Vadsbyvej) revealed a very complex system where diffusion, biotic and abiotic degradation processes occurred simultaneously. High resolution sub sampling with combined use of chemical analysis, molecular microbial tools and CSIA was necessary to identify both biotic and abiotic...

  17. The geochemistry of stable chlorine and bromine isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Eggenkamp, Hans [Onderzock and Beleving, Bussum (Netherlands)

    2014-11-01

    First book solely dedicated to the geochemistry of chlorine and bromine isotopes. Detailed description of analytical techniques, including their advantages and disadvantages. Indication of research fields where measurement of these isotopes is especially useful. This book provides detailed information on the history, analysis and applications of chlorine and bromine isotope geochemistry. Chlorine and bromine are geochemically unique as they prefer to exist as single charged negative ions. For this reason isotope fractionation reflects mostly processes that are not related to changes in the redox state and this fractionation is generally modest. The book will describe the processes that are most easily detected using these isotopes. Also isotope variations, and processes that cause them, measured in oxidised species such as perchlorates and in organic molecules will be described in this book.

  18. Survey of potential chlorine production processes. Final report

    Energy Technology Data Exchange (ETDEWEB)

    1979-04-01

    This report is part of the ongoing study of industrial electrochemical processes for the purpose of identifying methods of improving energy efficiencies. A computerized literature search of past and current chlorine generation methods was performed to identify basic chlorine production processes. Over 200 pertinent references are cited involving 20 separate and distinct chlorine processes. Each basic process is evaluated for its engineering and economic viability and energy efficiency. A flow diagram is provided for each basic process. Four criteria are used to determine the most promising processes: raw material availability, type and amount of energy required, by-product demand/disposal and status of development. The most promising processes are determined to be the membrane process (with and without catalytic electrodes), Kel-Chlor, Mobay (direct electrolysis of hydrogen chloride), the Shell process (catalytic oxidation of hydrogen chloride) and oxidation of ammonium chloride. Each of these processes is further studied to determine what activities may be pursued.

  19. Chlorination of Carbon Nanotubes Obtained on the Different Metal Catalysts

    Directory of Open Access Journals (Sweden)

    Iwona Pełech

    2013-01-01

    Full Text Available In this paper, a chlorination method is proposed for simultaneous purification and functionalization of carbon nanotubes, thus increasing their ability to use. Carbon nanotubes were obtained by CVD method through ethylene decomposition on the nanocrystalline iron or cobalt or bimetallic iron-cobalt catalysts. The effects of temperature (50, 250, and 450°C in the case of carbon nanotubes obtained on the Fe-Co catalyst and type of catalyst (Fe, Co, Fe/Co on the effectiveness of the treatment and functionalization were tested. The phase composition of the samples was determined using the X-ray diffraction method. The quantitative analysis of metal impurity content was validated by means of the thermogravimetric analysis. Using X-ray Photoelectron Spectroscopy (XPS, Energy Dispersive Spectroscopy (EDS analysis, and also Mohr titration method, the presence of chlorine species on the surface of chlorinated samples was confirmed.

  20. Supplying sodium and chlorine is effective on patients with congestive heart failure

    Institute of Scientific and Technical Information of China (English)

    Yu Li; Changcong Cui

    2005-01-01

    Objective: To analyze the relationship of severity of heart failure and the concentration of serum sodium(Na + ) and chlorine(Cl- ) and to explore the effect of supplying sodium and chlorine on patients with Congestive heart failure. Methods: 80 patients with congestive heart failure were divided into two groups, namely supplying and control group. Serum sodium and chlorine were measured in all these patients. All treatments but supplying sodium and chlorine were same between the supplying and control groups. Results:According to NYHA, patients who were in class Ⅳ had lower level of serum sodium and chlorine than those in class Ⅱ ( P < 0.05). The heart function was improved after the level of serum sodium and chlorine were raised. Conclusions: The concentration of serum sodium and chlorine relates to the severity of heart failure. The therapy of supplying sodium and chlorine is an effective way to decrease death rate.

  1. 76 FR 62149 - American Chemistry Council, The Chlorine Institute, Inc., the Fertilizer Institute, and PPG...

    Science.gov (United States)

    2011-10-06

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF TRANSPORTATION Surface Transportation Board American Chemistry Council, The Chlorine Institute, Inc., the Fertilizer... American Chemistry Council, The Chlorine Institute, Inc., The Fertilizer Institute (TFI), and...

  2. Toxicity of chlorine dioxide to early life stages of marine organisms

    Energy Technology Data Exchange (ETDEWEB)

    Hose, J.E.; Di Fiore, D.; Parker, H.S.; Sciarrotta, T.

    1989-03-01

    With increasing interest in minimizing exposure to chlorine, many electric generating and water treatment plants are exploring the use of alternative biocides such as chlorine dioxide. Unlike chlorine, chlorine dioxide does not react with ambient organic compounds to form potentially carcinogenic trihalomethanes such as chloroform. However, the toxicity of chlorine dioxide to aquatic organisms has received little study. No information exists on chlorine toxicity to marine organisms. Furthermore, West Coast electric power stations usually discharge chlorine intermittently once or twice daily and substantial mixing of receiving water occurs between treatments. Therefore, this study sought to obtain information on chlorine dioxide toxicity using an exposure schedule typical of generating stations which discharge into the marine environment. Early life history stages of a plant, invertebrate and fish were tested since these stages are generally acknowledged to be most sensitive to toxicants and are the stages that are most likely to be exposed to the effluent.

  3. Chlorine release from biomass. Part 6; Kloravgaang fraan biobraenslen. Del 6

    Energy Technology Data Exchange (ETDEWEB)

    Zintl, Frank; Stroemberg, Birgitta [TPS Termiska Processer AB, Nykoeping (Sweden)

    2000-04-01

    Chlorine release from model compounds and different biomass fuels has been studied during thermal treatment in an electric oven in inert atmosphere (N{sub 2}) and with addition of 10% O{sub 2}. The amount of chlorine in all investigated materials has been kept to 2% with addition of KCl solution in methanol. The amount of chlorine was analysed before and after treatment in the decided atmosphere and to the temperature chosen. The influence from different functional groups on the chlorine release at low temperatures has been studied in pyrolysis experiments of simple model compounds with different structures. A good correlation between the chlorine release and the functional groups in the model substances was achieved. Results from the experiments shows that the early chlorine release, is most likely to occur in all biofuels, since all biomass fuels contains biological material with significant amounts of functional groups which can interact with fuel chlorine ( inorganic chlorine)

  4. [The effect of long-term external ionizing radiation on the functional activity of rat thyroid under enhanced potassium iodide consumption].

    Science.gov (United States)

    Lupachik, S V; Nadol'nik, L I

    2008-01-01

    The study was devoted to the effect of long-term (20 days) external ionizing radiation at a dose of 0.5 Gy on the iodide metabolism in the rat thyroid under supplementation of high iodine doses (10 daily KI doses). It was found that the potassium iodide administration partially prevented the effects of a post radiation decrease of serum thyroid hormone levels (the level of T4 was normal and that of T3 was 77.4% of the controls). After the supplementation of 10 daily iodide doses, the rat thyroid tissue showed the most pronounced increase in the levels of total, free and protein-bound iodide compared to the groups of animals consuming normal and elevated KI doses. Pronounced inhibition of thyroid peroxidase activity (3.1-fold) was noted in the same group. The data obtained indicate a radiation-induced activation of iodide uptake during its enhanced supplementation and disturbed iodide enzymatic oxidation and organification.

  5. An unusual case of reversible acute kidney injury due to chlorine dioxide poisoning.

    Science.gov (United States)

    Bathina, Gangadhar; Yadla, Manjusha; Burri, Srikanth; Enganti, Rama; Prasad Ch, Rajendra; Deshpande, Pradeep; Ch, Ramesh; Prayaga, Aruna; Uppin, Megha

    2013-09-01

    Chlorine dioxide is a commonly used water disinfectant. Toxicity of chlorine dioxide and its metabolites is rare. In experimental studies, it was shown that acute and chronic toxicity were associated with insignificant hematological changes. Acute kidney injury due to chlorine dioxide was not reported. Two cases of renal toxicity due to its metabolites, chlorate and chlorite were reported. Herein, we report a case of chlorine dioxide poisoning presenting with acute kidney injury.

  6. Chlorine dioxide water disinfection: a prospective epidemiology study

    Energy Technology Data Exchange (ETDEWEB)

    Michael, G.E.; Miday, R.K.; Bercz, J.P.; Miller, R.G.; Greathouse, D.G.; Kraemer, D.F.; Lucas, J.B.

    1981-01-01

    An epidemiologic study of 198 persons exposed for 3 months to drinking water disinfected with chlorine dioxide was conducted in a rural village. A control population of 118 nonexposed persons was also studied. Pre-exposure hematologic and serum chemical parameters were compared with test results after 115 days of exposure. Chlorite ion levels in the water averaged approximately 5 ppM during the study period. Statistical analysis (ANOVA) of the data failed to identify any significant exposure-related effects. This study suggests that future evaluations of chlorine dioxide disinfection should be directed toward populations with potentially increased sensitivity to hemolytic agents.

  7. Kinetics and Mechanism of Bacterial Disinfection by Chlorine Dioxide1

    Science.gov (United States)

    Benarde, Melvin A.; Snow, W. Brewster; Olivieri, Vincent P.; Davidson, Burton

    1967-01-01

    Survival data are presented for a fecal strain of Escherichia coli exposed to three concentrations of chlorine dioxide at four temperatures. Chick's first-order reaction equation is generalized to a pseudo nth-order model. Nonlinear least squares curve-fitting of the survival data to the nth order model was performed on an analogue computer. The data were observed to follow fractional order kinetics with respect to survival concentration, with an apparent activation energy of 12,000 cal/mole. Initial experiments support the thesis that the mechanism of chlorine dioxide kill occurs via disruption of protein synthesis. Images Fig. 1 Fig. 2 Fig. 3 PMID:5339839

  8. Thermodynamic equilibrium diagram of the chlorine-titanium system

    Institute of Scientific and Technical Information of China (English)

    DU Ailing; GUO Xiaofei; ZHANG Heming; LIU Jiang

    2005-01-01

    The chemical and electrochemical equilibria of the chlorine-titanium system in the presence of gaseous phase were investigated. Many species, which consisted of chlorine and titanium, were considered. Various thermodynamic equilibria were calculated in the different pressures at different temperatures. The calculated results were shown as log p-1/T and E-T diagrams. These diagrams may be used as important tools for corrosion study and titanium production. The diagrams are also used to thermodynamically determine the existence areas of various species and so on.

  9. Sonochemical Treatment of Water Polluted by Chlorinated Organocompounds. A Review

    Directory of Open Access Journals (Sweden)

    Olivier Louisnard

    2010-02-01

    Full Text Available As one of several types of pollutants in water, chlorinated compounds have been routinely subjected to sonochemical analysis to check the environmental applications of this technology. In this review, an extensive study of the influence of the initial concentration, ultrasonic intensity and frequency on the kinetics, degradation efficiency and mechanism has been analyzed. The sonochemical degradation follows a radical mechanism which yields a very wide range of chlorinated compounds in very low concentrations. Special attention has been paid to the mass balance comparing the results from several analytical techniques. As a conclusion, sonochemical degradation alone is not an efficient treatment to reduce the organic pollutant level in waste water.

  10. Oxidation of pharmaceuticals by chlorine dioxide in biologically treated wastewater

    DEFF Research Database (Denmark)

    Hey, G.; Grabic, R.; Ledin, A.

    2012-01-01

    Biologically treated wastewater spiked with a mixture of 56 active pharmaceutical ingredients (APIs) was treated with 0–20mg/L chlorine dioxide (ClO2) solution in laboratory-scale experiments. Wastewater effluents were collected from two wastewater treatment plants in Sweden, one with extended......O2, while in high COD effluent a significant increase in API oxidation was observed after treatment with 8mg/L ClO2. This study illustrates the successful degradation of several APIs during treatment of wastewater effluents with chlorine dioxide....

  11. Chlorine international thermodynamic tables of the fluid state

    CERN Document Server

    Angus, S; de Reuck, K M

    1985-01-01

    Chlorine: International Thermodynamic Tables of the Fluid State-8 is a four-chapter book that covers available and estimated data on chlorine; estimation of the element's properties; the correlating equations for the element; and how the tabulated properties are calculated from chosen equation. The tables in this book give the volume, entropy, enthalpy, isobaric heat capacity, compression factor, fugacity/pressure ratio, Joule-Thomson coefficient, ratio of the heat capacities, and speed of sound as a function of pressure and temperature. Given in the tables as well are the pressure, entropy, i

  12. Chlorine cell disinfection determination with flow cell cytometry and plate count (poster)

    NARCIS (Netherlands)

    Peters, M.C.F.M.; Keuten, M.G.A.; De Kreuk, M.K.; Van Loosdrecht, M.C.M.; Rietveld, L.C.

    2013-01-01

    Chlorine is used for disinfection in different water systems. This research focuses on chlorine disinfection in swimming pool water. In the Netherlands, free available chlorine concentrations in swimming pools are limited between 0.5-1.5 mg/L, which is based on a 4-log removal of Pseudomonas aerugin

  13. Estimates of Gibbs free energies of formation of chlorinated aliphatic compounds

    NARCIS (Netherlands)

    Dolfing, Jan; Janssen, Dick B.

    1994-01-01

    The Gibbs free energy of formation of chlorinated aliphatic compounds was estimated with Mavrovouniotis' group contribution method. The group contribution of chlorine was estimated from the scarce data available on chlorinated aliphatics in the literature, and found to vary somewhat according to the

  14. [The analysis for silver iodide fine particles of TLC/FTIR matrix].

    Science.gov (United States)

    Zhu, Qing; Su, Xiao; Wu, Hai-Jun; Zhai, Yan-Jun; Xia, Jin-Ming; Buhebate; Xu, Yi-Zhuang; Wu, Jin-Guang

    2012-07-01

    In situ TLC/FTIR technique has tremendous potential in the analysis of complex mixtures. However, the progress in this technique was quite slow. The reason is that conventional stationary phase has strong absorption in FTIR spectrum and thus brings about severe interference in the detection of samples. To solve the problem, the authors propose to use AgI fine particles as stationary phase of TLC plate. The reasons are as follows: Silver iodide fine particles have no absorbance in an IR region between 4 000 and 800 cm(-1), therefore, the interference caused by IR absorption of stationary phase can be removed. Moreover, silver iodide is stable and insolvable in water and organic solvents and thus it will not be destroyed by mobile phase or react with samples during the TLC separation. To improve TLC separation efficiency and quality of FTIR spectra during the TLC/FTIR analysis, the size of AgI particles should be below 500 nm. We used orthogonal design approach to optimize the experimental condition to AgI particles so that the average size of AgI particles is around 100 nm. No absorption of impurity or adsorbed water were observed in FTIR spectrum of the AgI particles the authors used "settlement volatilization method" to prepare TLC plate without using polymeric adhesive that may bring about significant interference in FTIR analysis. Preliminary TLC experiments proved that the TLC plate using AgI fine particles as stationary phase can separate mixtures of rhodamine B and bromophenol blue successfully. Applications of silver iodide fine particles as stationary phase have bright perspective in the development of in-situ TLC/FTIR analysis techniques.

  15. Titrimetric and spectrophotometric assay of diethylcarbamazine citrate in formulations using iodate and iodide mixture as reagents

    Directory of Open Access Journals (Sweden)

    Nagaraju Swamy

    2015-03-01

    Full Text Available One titrimetric and two spectrophotometric methods are proposed for the determination of diethylcarbamazine citrate (DEC in bulk drug and in formulations using potassium iodate and potassium iodide as reagent. The methods employ the well-known analytical reaction between iodate and iodide in the presence of acid. In titrimetry (method A, the drug was treated with a measured excess of thiosulfate in the presence of unmeasured excess of iodate-iodide mixture and after a standing time of 10 min, the surplus thiosulfate was determined by back titration with iodine towards starch end point. Titrimetric assay is based on a 1:3 reaction stoichiometry between DEC and iodine and the method is applicable over 2.0-10.0 mg range. The liberated iodine is measured spectrophotometrically at 370 nm (method B or the iodine-starch complex measured at 570 nm (method C. In both methods, the absorbance is found to be linearly dependent on the concentration of iodine, which in turn is related to DEC concentration. The calibration curves are linear over 2.5-50 and 2.5-30 µg mL-1 DEC for method B and method C, respectively. The calculated molar absorptivity and Sandell sensitivity values were 6.48×103 L mol-1 cm-1 and 0.0604 µg cm-2, respectively, for method B, and their respective values for method C are 9.96×103 L mol-1 cm-1 and 0.0393 µg cm-2. The intra-day and inter-day accuracy and precision studies were carried out according to the ICH guidelines. The methods were successfully applied to the analysis of DEC formulations.

  16. Equations of state for crystalline zirconium iodide: The role of dispersion

    Energy Technology Data Exchange (ETDEWEB)

    Rossi, Matthew L., E-mail: mrossi@lanl.gov [Materials Science and Technology, MST-6, Los Alamos National Lab, Los Alamos, NM (United States); Taylor, Christopher D. [Materials Science and Technology, MST-6, Los Alamos National Lab, Los Alamos, NM (United States)

    2013-02-15

    We present the first-principle equations of state of several zirconium iodides, ZrI{sub 2}, ZrI{sub 3}, and ZrI{sub 4}, computed using density functional theory methods that apply various methods for introducing the dispersion correction. Iodides formed due to reaction of molecular or atomic iodine with zirconium and zircaloys are of particular interest due to their application to the cladding material used in the fabrication of nuclear fuel rods. Stress corrosion cracking (SCC), associated with fission product chemistry with the clad material, is a major concern in the life cycle of nuclear fuels, as many of the observed rod failures have occurred due to pellet–cladding chemical interactions (PCCI) [A. Atrens, G. Dannhäuser, G. Bäro, Stress-corrosion-cracking of zircaloy-4 cladding tubes, Journal of Nuclear Materials 126 (1984) 91–102; P. Rudling, R. Adamson, B. Cox, F. Garzarolli, A. Strasser, High burn-up fuel issues, Nuclear Engineering and Technology 40 (2008) 1–8]. A proper understanding of the physical properties of the corrosion products is, therefore, required for the development of a comprehensive SCC model. In this particular work, we emphasize that, while existing modeling techniques include methods to compute crystal structures and associated properties, it is important to capture intermolecular forces not traditionally included, such as van der Waals (dispersion) correction. Furthermore, crystal structures with stoichiometries favoring a high I:Zr ratio are found to be particularly sensitive, such that traditional density functional theory approaches that do not incorporate dispersion incorrectly predict significantly larger volumes of the lattice. This latter point is related to the diffuse nature of the iodide electron cloud.

  17. The sphingosine 1-phosphate receptor modulator FTY720 prevents iodide-induced autoimmune thyroiditis in non-obese diabetic mice.

    Science.gov (United States)

    Morohoshi, Kazuki; Osone, Michiko; Yoshida, Katsumi; Nakagawa, Yoshinori; Hoshikawa, Saeko; Ozaki, Hiroshi; Takahashi, Yurie; Ito, Sadayoshi; Mori, Kouki

    2011-09-01

    FTY720 is an immunomodulator that alters migration and homing of lymphocytes via sphingosine 1-phosphate receptors. This compound has been shown to be effective in suppressing autoimmune diseases in experimental and clinical settings. In the present study, we tested whether FTY720 prevented autoimmune thyroiditis in iodide-treated non-obese diabetic (NOD) mice, a model of Hashimoto's thyroiditis (HT) in humans. Mice were given 0.05% iodide water for 8 weeks, and this treatment effectively induced thyroiditis. Iodide-treated mice were injected intraperitoneally with either saline or FTY720 during the iodide treatment. FTY720 clearly suppressed the development of thyroiditis and reduced serum anti-thyroglobulin antibody levels. The number of circulating lymphocytes and spleen cells including CD4(+) T cells, CD8(+) T cells, and CD4(+)Foxp3(+) T cells was decreased in FTY720-treated mice. Our results indicate that FTY720 has immunomodulatory effects on iodide-induced autoimmune thyroiditis in NOD mice and may be a potential candidate for use in the prevention of HT.

  18. Crystal Growth and Dissolution of Methylammonium Lead Iodide Perovskite in Sequential Deposition: Correlation between Morphology Evolution and Photovoltaic Performance.

    Science.gov (United States)

    Hsieh, Tsung-Yu; Huang, Chi-Kai; Su, Tzu-Sen; Hong, Cheng-You; Wei, Tzu-Chien

    2017-03-01

    Crystal morphology and structure are important for improving the organic-inorganic lead halide perovskite semiconductor property in optoelectronic, electronic, and photovoltaic devices. In particular, crystal growth and dissolution are two major phenomena in determining the morphology of methylammonium lead iodide perovskite in the sequential deposition method for fabricating a perovskite solar cell. In this report, the effect of immersion time in the second step, i.e., methlyammonium iodide immersion in the morphological, structural, optical, and photovoltaic evolution, is extensively investigated. Supported by experimental evidence, a five-staged, time-dependent evolution of the morphology of methylammonium lead iodide perovskite crystals is established and is well connected to the photovoltaic performance. This result is beneficial for engineering optimal time for methylammonium iodide immersion and converging the solar cell performance in the sequential deposition route. Meanwhile, our result suggests that large, well-faceted methylammonium lead iodide perovskite single crystal may be incubated by solution process. This offers a low cost route for synthesizing perovskite single crystal.

  19. Electrical properties of solid iodo mercurates resulting from the reaction of HgI2 with alcaline iodides

    Science.gov (United States)

    Ponpon, J. P.; Amann, M.

    2005-01-01

    Potassium iodide solutions are currently used during the fabrication process of mercuric iodide based nuclear radiation detectors. However, KI treatment leaves the HgI2 surface covered with a residual compound (namely the potassium tri-iodo mercurate) which has a significant influence on the surface properties and stability of mercuric iodide devices and therefore on the detectors characteristics. Looking for other solutions to etch mercuric iodide, we found it interesting to investigate the electrical properties of the compounds which may form when etching HgI2 in NH4I, NaI, and RbI. For this purpose, solid iodo mercurates with the cations ammonium, sodium, and rubidium, have been prepared by reacting HgI2 with the solutions of interest. Study of the electrical properties of these samples and comparison with those of potassium tri-iodo mercurate ones, especially with respect to humidity, indicates noticeable stability differences in presence of water vapour. This could have interesting consequences on the surface cleaning of mercuric iodide.

  20. A novel vortex-assisted liquid-liquid microextraction approach using auxiliary solvent: Determination of iodide in mineral water samples.

    Science.gov (United States)

    Zaruba, Serhii; Vishnikin, Andriy B; Andruch, Vasil

    2016-01-01

    A novel vortex-assisted liquid-liquid microextraction (VA-LLME) for determination of iodide was developed. The method includes the oxidation of iodide with iodate in the presence of hydrochloric acid followed by VA-LLME of the ion-pair formed between ICl2(-) and Astra Phloxine reagent (AP) and subsequent absorbance measurement at 555nm. The appropriate experimental conditions were investigated and found to be: 5mL of sample, 0.27molL(-)(1) HCl, 0.027mmolL(-1) KIO3 as the oxidation agent, 250μL of extraction mixture containing amyl acetate as the extraction solvent and carbon tetrachloride as the auxiliary solvent (1:1, v/v), 0.04mmolL(-1) AP reagent, vortex time: 20s at 3000rpm, centrifugation: 4min at 3000rpm. The calibration plot was linear in the range 16.9-169μg L(-1) of iodide, with a correlation coefficient (R(2)) of 0.996, and the relative standard deviation ranged from 1.9 to 5.7%. The limit of detection (LOD) and limit of quantification (LOQ) were 1.75 and 6.01μgL(-)(1) of iodide, respectively. The suggested procedure was applied for determination of iodide in real mineral water samples.

  1. An iodine supplementation of tomato fruits coated with an edible film of the iodide-doped chitosan.

    Science.gov (United States)

    Limchoowong, Nunticha; Sricharoen, Phitchan; Techawongstien, Suchila; Chanthai, Saksit

    2016-06-01

    In general, the risk of numerous thyroid cancers inevitably increases among people with iodine deficiencies. An iodide-doped chitosan (CT-I) solution was prepared for dipping tomatoes to coat the fresh surface with an edible film (1.5 μm), thereby providing iodine-rich fruits for daily intake. Characterisation of the thin film was conducted by FTIR and SEM. Stability of the CT-I film was studied via water immersion at various time intervals, and no residual iodide leached out due to intrinsic interactions between the cationic amino group of chitosan and iodide ions. Moreover, the iodide supplement exhibited no effect on the antioxidant activity of tomatoes. The iodine content in the film-coated tomato was determined by ICP-OES. The tomato coating with 1.5% (w/v) CT-I contained approximately 0.4 μg iodide per gram fresh weight. In addition, the freshness and storability of iodine-doped tomatoes were also maintained for shelf-life concerns.

  2. 21 CFR 177.2430 - Polyether resins, chlorinated.

    Science.gov (United States)

    2010-04-01

    ...) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use Only as... producing, manufacturing, packing, processing, preparing, treating, packaging, transporting, or holding food... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyether resins, chlorinated. 177.2430 Section...

  3. Chlorinated Iridoid Glucosides from Veronica longifolia and their Antioxidant Activity

    DEFF Research Database (Denmark)

    Jensen, Søren Rosendal; Gotfredsen, Charlotte Held; Harput, U. Sebnem;

    2010-01-01

    From Veronica longifolia were isolated three chlorinated iridoid glucosides, namely asystasioside E (6) and its 6-O-esters 6a and 6b, named longifoliosides A and B, respectively. The structures of 6a and 6b were proved by analysis of their spectroscopic data and by conversion to the catalpol este...

  4. Riverine input of chlorinated hydrocarbons in the coastal pollution

    Digital Repository Service at National Institute of Oceanography (India)

    Sarkar, A.; Everaarts, J.M.

    of various chlorinated hydrocarbons. It deals with an in-depth analysis of pollution of the coastal ecosystem around the Netherlands, U.K. and Germany due to inputs of contaminants from the rivers namely, Elbe, Weser, Ems Ijssel, Rhine, Meuse, Scheldt, Thames...

  5. Physical property determinations of short chain chlorinated paraffins

    Energy Technology Data Exchange (ETDEWEB)

    Drouillard, K.G.D. [Univ. of Manitoba, Winnipeg, Manitoba (Canada). Dept. of Soil Science; Hiebert, T.; Friesen, K.J. [Univ. of Winnipeg, Manitoba (Canada). Dept. of Chemistry; Muir, D.C.G. [Freshwater Inst., Winnipeg, Manitoba (Canada)

    1995-12-31

    Chlorinated paraffins (CP) are chlorinated derivatives of n-alkanes commonly utilized in commercial formulations of flame retardants, plasticizers and high pressure lubricants. Recent reviews on CPs have expressed concern regarding the potential toxicity and carcinogenic properties of these compounds. Of the various classes of CPs, short chain compounds (carbon chain lengths 10 to 13) appear to pose the greatest risk. There is little data available concerning key physical properties of CPs required to assess their environmental behavior and mobility. In this study, water solubilities, dissolved organic matter water partition coefficients (K{sub DOM}) and Henry`s Law constants were determined for short chain chlorinated paraffins by generator column, apparent solubility enhancement and gas-purging techniques. Water solubilities were determined for synthesized, isolated products of polychlorinated decanes, undecanes and dodecanes. Solubilities at 25 C were on the order of 2 to 140 {micro}g/L for tetra- to hexachlorodecane products. The Henry`s Law constants for tetra- and pentachlorodecane were determined to be 6.6 {+-} 0.6 and 3.5 {+-} 0.6 Pa{center_dot}m{sup 3}{center_dot}mol{sup {minus}1} respectively. Relationships between carbon chain length and degree of chlorination on the determined physical properties will be discussed.

  6. Chlorine stress mediates microbial surface attachment in drinking water systems.

    Science.gov (United States)

    Liu, Li; Le, Yang; Jin, Juliang; Zhou, Yuliang; Chen, Guowei

    2015-03-01

    Microbial attachment to drinking water pipe surfaces facilitates pathogen survival and deteriorates disinfection performance, directly threatening the safety of drinking water. Notwithstanding that the formation of biofilm has been studied for decades, the underlying mechanisms for the origins of microbial surface attachment in biofilm development in drinking water pipelines remain largely elusive. We combined experimental and mathematical methods to investigate the role of environmental stress-mediated cell motility on microbial surface attachment in chlorination-stressed drinking water distribution systems. Results show that at low levels of disinfectant (0.0-1.0 mg/L), the presence of chlorine promotes initiation of microbial surface attachment, while higher amounts of disinfectant (>1.0 mg/L) inhibit microbial attachment. The proposed mathematical model further demonstrates that chlorination stress (0.0-5.0 mg/L)-mediated microbial cell motility regulates the frequency of cell-wall collision and thereby controls initial microbial surface attachment. The results reveal that transport processes and decay patterns of chlorine in drinking water pipelines regulate microbial cell motility and, thus, control initial surface cell attachment. It provides a mechanistic understanding of microbial attachment shaped by environmental disinfection stress and leads to new insights into microbial safety protocols in water distribution systems.

  7. Inactivation of human and simian rotaviruses by chlorine dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Yu-Shiaw (Brookhaven National Lab., Upton, NY (USA)); Vaughn, J.M. (Univ. of New England College of Medicine, Biddeford, ME (USA))

    1990-05-01

    The inactivation of single-particle stocks of human (type 2, Wa) and simian (SA-11) rotaviruses by chlorine dioxide was investigated. Experiments were conducted at 4{degree}C in a standard phosphate-carbonate buffer. Both virus types were rapidly inactivated, within 20 s under alkaline conditions, when chlorine dioxide concentrations ranging from 0.05 to 0.2 mg/liter were used. Similar reductions of 10{sup 5}-fold in infectivity required additional exposure time of 120 s at 0.2 mg/liter for Wa and at 0.5 mg/liter for SA-11, respectively, at pH 6.0. The inactivation of both virus types was moderate a neutral pH, and the sensitivities to chlorine dioxide were similar. The observed enhancement of virucidal efficiency with increasing pH was contrary to earlier findings with chlorine- and ozone-treated rotavirus particles, where efficiencies decreased with increasing alkalinity. Comparison of 99.9% virus inactivation times revealed ozone to be the most effective virucidal agent among these three disinfectants.

  8. Inactivation of human and simian rotaviruses by chlorine dioxide.

    Science.gov (United States)

    Chen, Y S; Vaughn, J M

    1990-01-01

    The inactivation of single-particle stocks of human (type 2, Wa) and simian (SA-11) rotaviruses by chlorine dioxide was investigated. Experiments were conducted at 4 degrees C in a standard phosphate-carbonate buffer. Both virus types were rapidly inactivated, within 20 s under alkaline conditions, when chlorine dioxide concentrations ranging from 0.05 to 0.2 mg/liter were used. Similar reductions of 10(5)-fold in infectivity required additional exposure time of 120 s at 0.2 mg/liter for Wa and at 0.5 mg/liter for SA-11, respectively, at pH 6.0. The inactivation of both virus types was moderate at neutral pH, and the sensitivities to chlorine dioxide were similar. The observed enhancement of virucidal efficiency with increasing pH was contrary to earlier findings with chlorine- and ozone-treated rotavirus particles, where efficiencies decreased with increasing alkalinity. Comparison of 99.9% virus inactivation times revealed ozone to be the most effective virucidal agent among these three disinfectants. PMID:2160222

  9. Structural and optical properties of chlorinated plasma polymers

    Energy Technology Data Exchange (ETDEWEB)

    Turri, Rafael [Laboratorio de Plasmas Tecnologicos, Campus Experimental de Sorocaba, Universidade Estadual Paulista (UNESP), Avenida Tres de Marco 511, Alto de Boa Vista, 18087-180, Sorocaba, SP (Brazil); Davanzo, Celso U. [Instituto de Quimica, Universidade Estadual de Campinas, Campinas, SP (Brazil); Schreiner, Wido [Departamento de Fisica, Universidade Federal de Parana, PR (Brazil); Dias da Silva, Jose Humberto [Faculdade de Ciencias, Universidade Estadual Paulista (UNESP), Bauru, SP (Brazil); Appolinario, Marcelo Borgatto [Laboratorio de Plasmas Tecnologicos, Campus Experimental de Sorocaba, Universidade Estadual Paulista (UNESP), Avenida Tres de Marco 511, Alto de Boa Vista, 18087-180, Sorocaba, SP (Brazil); Durrant, Steven F., E-mail: steve@sorocaba.unesp.br [Laboratorio de Plasmas Tecnologicos, Campus Experimental de Sorocaba, Universidade Estadual Paulista (UNESP), Avenida Tres de Marco 511, Alto de Boa Vista, 18087-180, Sorocaba, SP (Brazil)

    2011-12-30

    Amorphous hydrogenated chlorinated carbon (a-C:H:Cl) films were produced by the plasma polymerization of chloroform-acetylene-argon mixtures in a radiofrequency plasma enhanced chemical vapor deposition system. The main parameter of interest was the proportion of chloroform in the feed, R{sub C}, which was varied from 0 to 80%. Deposition rates of 80 nm min{sup -1} were typical for the chlorinated films. Infrared reflection-absorption spectroscopy revealed the presence of C-Cl groups in all the films produced with chloroform in the feed. X-ray photoelectron spectroscopy confirmed this finding, and revealed a saturation of the chlorine content at {approx} 47 at.% for R{sub C} {>=} 40%. The refractive index and optical gap, E{sub 04}, of the films were roughly in the 1.6 to 1.7, and the 2.8 to 3.7 eV range. These values were calculated from transmission ultraviolet-visible-near infrared spectra. Chlorination leads to an increase in the water surface contact angle from {approx} 40 Degree-Sign to {approx} 77 Degree-Sign .

  10. Biodegradation of chlorinated solvents in a water unsaturated topsoil

    DEFF Research Database (Denmark)

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

    2003-01-01

    In order to investigate topsoils as potential sinks for chlorinated solvents from the atmosphere, the degradation of trichloromethane (CHCl3), 1,1,1-trichloroethane (CH3CCl3), tetrachloromethane (CCl4), trichloroethene (C2HCl3) and tetrachloroethene (C2Cl4) was studied in anoxic laboratory experi...

  11. Transformation of Chlorinated Hydrocarbons on Synthetic Green Rusts

    Science.gov (United States)

    Green rusts (GRs) are layered double hydroxides that contain both ferrous and ferric ions in their structure. GRs can potentially serve as a chemical reductant for degradation of chlorinated hydrocarbons. GRs are found in zerovalent iron based permeable reactive barriers and in c...

  12. Release of Chlorine and Sulfur during Biomass Torrefaction and Pyrolysis

    DEFF Research Database (Denmark)

    Saleh, Suriyati Binti; Flensborg, Julie Pauline; Shoulaifar, Tooran Khazraie

    2014-01-01

    -forming elements were torrefied/pyrolyzed in the temperature range of 150-500 degrees C. The relative release of chlorine and sulfur was calculated based on mass balance and analysis of the biomass before and after torrefaction. In selected cases, measurement of methyl chloride (CH3Cl) in the gas from straw...

  13. Transformation of chlorinated compounds by methanogenic granular sludge

    NARCIS (Netherlands)

    Eekert, van M.H.A.

    1999-01-01

    Chlorinated compounds are an important group of contaminants often found in sediments, groundwater, soils, wastewaters, and off-gasses. Many of these pollutants are found on the EPA list of Priority Pollutants indicating their potential hazard for the environment. Initial degradation can occur via d

  14. Degradation of Chlorinated Aromatic Compounds in UASB Reactors

    DEFF Research Database (Denmark)

    Christiansen, Nina; Hendriksen, Hanne Vang; Järvinen, Kimmo T.;

    1995-01-01

    Data on anaerobic degradation of chloroaromatic compounds in Upflow Anaerobic Sludge Blanket Reactors (UASB-reactor) are presented and compared. Special attention is given to the metabolic pathways for degradation of chlorinated phenols by granular sludge. Results indicate that PCP can be degraded...

  15. ANALYSIS OF NASAL TISSUE FOR BIOMARKERS OF CHLORINE EXPOSURE

    Science.gov (United States)

    Both 3-chloro-tyrosine (CT) and 3,5-dichloro-tyrosine (dCT) are sensitive and specific biomarkers for evaluating exposure to chlorine gas (Cl2) and hypochlorous acid (HOCl). Previous investigations have focused on the formation of CT and dCT resulting from biochemical responses ...

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

    Science.gov (United States)

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

    2015-01-01

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

  17. Electrochemical chlorine evolution at rutile oxide (110) surfaces

    DEFF Research Database (Denmark)

    Hansen, Heine Anton; Man, Isabela Costinela; Studt, Felix;

    2010-01-01

    of the oxygen binding energy, giving rise to a Sabatier volcano. By combining the surface phase diagram and the volcano describing the catalytic activity, we find that the reaction mechanism differs depending on catalyst material. The flexibility in reaction path means that the chlorine evolution activity...

  18. Disinfection byproduct yields from the chlorination of natural waters

    Science.gov (United States)

    Rathbun, R.E.

    1996-01-01

    Yields for the formation of trihalomethane and nonpurgeable total organic-halide disinfection byproducts were determined as a function of pH and initial free-chlorine concentration for the chlorination of water from the Mississippi, Missouri, and Ohio Rivers. Samples were collected at 12 sites on the Mississippi River from Minneapolis, MN, to New Orleans. LA, and on the Missouri and Ohio Rivers 1.6 km above their confluences with the Mississippi during the summer, fall, and spring seasons of the year. Yields varied little with distance along the Mississippi River, although the dissolved organic-carbon concentration decreased considerably with distance downstream. Yields for the Missouri and Ohio were comparable to yields for the Mississippi, despite much higher bromide concentrations for the Missouri and Ohio. Trihalomethane yields increased as the pH and initial free- chlorine concentration increased. Nonpurgeable total organic-halide yields also increased as the initial free-chlorine concentration increased, but decreased as the pH increased.

  19. Clustering chlorine reactivity of haloacetic acid precursors in inland lakes.

    Science.gov (United States)

    Zeng, Teng; Arnold, William A

    2014-01-01

    Dissolved organic matter (DOM) represents the major pool of organic precursors for harmful disinfection byproducts, such as haloacetic acids (HAAs), formed during drinking water chlorination, but much of it remains molecularly uncharacterized. Knowledge of model precursors is thus a prerequisite for understanding the more complex whole water DOM. The utility of HAA formation potential data from model DOM precursors, however, is limited due to the lack of comparability to water samples. In this study, the formation kinetics of dichloroacetic acid (DCAA) and trichloroacetic acid (TCAA), the two predominant HAA species, were delineated upon chlorination of seventeen model DOM precursors and sixty-eight inland lake water samples collected from the Upper Midwest region of the United States. Of particular interest was the finding that the DCAA and TCAA formation rate constants could be grouped into four statistically distinct clusters reflecting the core structural features of model DOM precursors (i.e., non-β-diketone aliphatics, β-diketone aliphatics, non-β-diketone phenolics, and β-diketone phenolics). A comparative approach built upon hierarchical cluster analysis was developed to gain further insight into the chlorine reactivity patterns of HAA precursors in inland lake waters as defined by the relative proximity to four model precursor clusters. This work highlights the potential for implementing an integrated kinetic-clustering approach to constrain the chlorine reactivity of DOM in source waters.

  20. The chlorine isotope fingerprint of the lunar magma ocean.

    Science.gov (United States)

    Boyce, Jeremy W; Treiman, Allan H; Guan, Yunbin; Ma, Chi; Eiler, John M; Gross, Juliane; Greenwood, James P; Stolper, Edward M

    2015-09-01

    The Moon contains chlorine that is isotopically unlike that of any other body yet studied in the Solar System, an observation that has been interpreted to support traditional models of the formation of a nominally hydrogen-free ("dry") Moon. We have analyzed abundances and isotopic compositions of Cl and H in lunar mare basalts, and find little evidence that anhydrous lava outgassing was important in generating chlorine isotope anomalies, because (37)Cl/(35)Cl ratios are not related to Cl abundance, H abundance, or D/H ratios in a manner consistent with the lava-outgassing hypothesis. Instead, (37)Cl/(35)Cl correlates positively with Cl abundance in apatite, as well as with whole-rock Th abundances and La/Lu ratios, suggesting that the high (37)Cl/(35)Cl in lunar basalts is inherited from urKREEP, the last dregs of the lunar magma ocean. These new data suggest that the high chlorine isotope ratios of lunar basalts result not from the degassing of their lavas but from degassing of the lunar magma ocean early in the Moon's history. Chlorine isotope variability is therefore an indicator of planetary magma ocean degassing, an important stage in the formation of terrestrial planets.

  1. Towards Renewable Iodide Sources for Electrolytes in Dye-Sensitized Solar Cells

    Directory of Open Access Journals (Sweden)

    Iryna Sagaidak

    2016-03-01

    Full Text Available A novel family of iodide salts and ionic liquids based on different carbohydrate core units is herein described for application in dye-sensitized solar cell (DSC. The influence of the molecular skeleton and the cationic structure on the electrolyte properties, device performance and on interfacial charge transfer has been investigated. In combination with the C106 polypyridyl ruthenium sensitizer, power conversion efficiencies lying between 5.0% and 7.3% under standard Air Mass (A.M. 1.5G conditions were obtained in association with a low volatile methoxypropionitrile (MPN-based electrolyte.

  2. Performance of neutron activation analysis in the evaluation of bismuth iodide purification methodology

    Energy Technology Data Exchange (ETDEWEB)

    Armelin, Maria Jose A.; Ferraz, Caue de Mello; Hamada, Margarida M., E-mail: marmelin@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil). Lab. de Analise por Ativacao Neutronica

    2015-07-01

    Bismuth tri-iodide (BrI{sub 3}) is an attractive material for using as a semiconductor. In this paper, BiI{sub 3} crystals have been grown by the vertical Bridgman technique using commercially available powder. The impurities were evaluated by instrumental neutron activation analysis (INAA). The results show that INAA is an analytical method appropriate for monitoring the impurities of: Ag, As, Br, Cr, K, Mo, Na and Sb in the various stages of the BiI{sub 3} purification methodology. (author)

  3. Introduction to fifth international workshop on mercuric iodide nuclear radiation detectors

    Energy Technology Data Exchange (ETDEWEB)

    Schieber, M.

    1982-01-01

    Mercuric iodide is a wide bandgap semiconductor, with Eg approx. = 2.14 eV at room temperature. Therefore, HgI/sub 2/ is totally different from the well-studied, narrower gap, elemental semiconductors such as Si and Ge, and also different in its physical and chemical properties from the known semiconductor binary zinc-blend compounds such as GaAs or InP. The purpose of studies in the last decade was to further our understanding of HgI/sub 2/; recent progress is reported. (WHK)

  4. Effects of Aromatic Ammoniums on Methyl Ammonium Lead Iodide Hybrid Perovskite Materials

    Directory of Open Access Journals (Sweden)

    Jianli Yang

    2017-01-01

    Full Text Available The introduction of bulky ammoniums into methyl ammonium lead iodide hybrid perovskites (MAPbI3 has emerged as a promising strategy to improve the properties of these materials. In the present work, we studied the effects of several aromatic ammoniums onto the structural, electronic, and optical properties of MAPbI3. Although powder XRD data suggest that the bulky cations are not involved in the bulk phase of the MAPbI3, a surprisingly large effect of the bulky cations onto the photoluminescence properties was observed.

  5. Nucleophilic addition to the ethynyl group in ethynylestradiol catalyzed by crown ether-copper (1) iodide.

    Science.gov (United States)

    Chen, S H; Luo, G R; Chang, X Z; Zhao, H M

    1991-10-01

    A new and convenient synthetic route to acetylation of estrogens is described. Benzo-15-crown-5 and cuprous iodide-mixed catalyst catalyzed the nucleophilic addition of 2,4-dibromoethynylestradiol, resulting in the formation of a new compound, 2,4-dibromo-17 alpha-acetylestradiol, of which the structure was characterized by infrared, UV, 1H nuclear magnetic resonance, mass spectra, and elemental analysis. It was found that the yield of this approach is much higher than that obtained in the hydration of usual acetylenic compounds.

  6. Subcutaneous Zygomycosis: A Report of One Case Responding Excellently to Potassium Iodide.

    Science.gov (United States)

    Mondal, Ashim Kr; Saha, Abhijit; Seth, Joly; Mukherjee, Soumya

    2015-01-01

    Subcutaneous Zygomycosis is a rare opportunistic fungal infection caused by Basidiobolus ranarum. Though this entity is endemic in South India, limited numbers of cases have been reported from this part of the country. We report a case of subcutaneous zygomycosis in a 25 year old lady who presented with a nontender, firm to hard swelling over the upper-left arm. Finger was easily inserted below the indurated edge. Histopathology revealed suppurative granuloma with aseptate hyphae. Patient responded excellently to saturated solution of potassium iodide in subsequent visits.

  7. Spectroscopy of stop bands in artificial opals filled with an alcohol solution of potassium iodide

    Science.gov (United States)

    Gorelik, V. S.; Filatov, V. V.

    2012-09-01

    The spectral position of the stop bands in photonic crystals based on artificial opals filled with an alcohol solution of potassium iodide is investigated. The energy-band structure of samples with quartz globules 230 nm in diameter is modeled based on the dispersion equation. The spectral position of the stop bands in the [111] direction at different solution concentrations is determined. The conditions for forbidden-band "collapse" are established. The possibility of applying artificial opals in optical cavities of lasers of different types is analyzed.

  8. Subcutaneous zygomycosis: A report of one case responding excellently to potassium iodide

    Directory of Open Access Journals (Sweden)

    Ashim Kr Mondal

    2015-01-01

    Full Text Available Subcutaneous Zygomycosis is a rare opportunistic fungal infection caused by Basidiobolus ranarum. Though this entity is endemic in South India, limited numbers of cases have been reported from this part of the country. We report a case of subcutaneous zygomycosis in a 25 year old lady who presented with a nontender, firm to hard swelling over the upper-left arm. Finger was easily inserted below the indurated edge. Histopathology revealed suppurative granuloma with aseptate hyphae. Patient responded excellently to saturated solution of potassium iodide in subsequent visits.

  9. Atypical Cutaneous Sporotrichosis in an Immunocompetent Adult: Response to Potassium Iodide.

    Science.gov (United States)

    Gandhi, Nikita; Chander, Ram; Jain, Arpita; Sanke, Sarita; Garg, Taru

    2016-01-01

    Cutaneous sporotrichosis, also known as "Rose Gardener's disease," caused by dimorphic fungus Sporothrix schenkii, is usually characterized by indolent nodular or nodulo-ulcerative lesions arranged in a linear pattern. We report bizarre nonlinear presentation of Sporotrichosis, in an immunocompetent adult occurring after a visit to Amazon rain forest, speculating infection with more virulent species of Sporothrix. The diagnosis was reached with the help of periodic acid-Schiff positive yeast cells and cigar shaped bodies seen in skin biopsy along with the therapeutic response to potassium iodide.

  10. Successful Therapy of Refractory Erythema Nodosum Associated with Crohn's Disease Using Potassium Iodide

    Directory of Open Access Journals (Sweden)

    John K Marshall

    1997-01-01

    Full Text Available Erythema nodosum is a common extraintestinal manifestation of Crohn's disease. While mild skin involvement often responds to conservative management, severe or refractory cases may require systemic corticosteroid or immunosuppressive therapy. This report describes successful treatment of severe, refractory erythema nodosum associated with Crohn's colitis using oral potassium iodide. While the mechanism of action of this agent is poorly understood, it appears to be an effective and nontoxic therapy for Crohn's-related erythema nodosum and warrants further evaluation in a placebo controlled trial.

  11. Growth and characterization of NLO crystal: L-leucine phthalic acid potassium iodide

    OpenAIRE

    Jagadeesh M.R.; Kumar H .M. Suresh; Kumari R. Ananda

    2015-01-01

    A new semi-organic non linear optical crystal, L-leucine phthalic acid potassium iodide (LLPPI) has been grown from an aqueous solution by slow evaporation method. The grown crystals were subjected to different characterizations, such as single crystal XRD, FT-IR, UV-Vis, TGA, SEM, EDAX, micro hardness, dielectric and powder SHG. Single crystal structure was determined from X-ray diffraction data and it revealed that the crystal belongs to triclinic system with the space group P1. The vibrati...

  12. Real-Time Observation of Organic Cation Reorientation in Methylammonium Lead Iodide Perovskites

    OpenAIRE

    2015-01-01

    This document is the Accepted Manuscript version of a Published Work that appeared in final form in The Journal of Physical Chemistry Letters, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://pubs.acs.org/doi/abs/10.1021/acs.jpclett.5b01555 The introduction of a mobile and polarized organic moiety as a cation in 3D lead-iodide perovskites brings fascinating optoelectronic properties to t...

  13. Atypical cutaneous sporotrichosis in an immunocompetent adult: Response to potassium iodide

    Directory of Open Access Journals (Sweden)

    Nikita Gandhi

    2016-01-01

    Full Text Available Cutaneous sporotrichosis, also known as “Rose Gardener's disease,” caused by dimorphic fungus Sporothrix schenkii, is usually characterized by indolent nodular or nodulo-ulcerative lesions arranged in a linear pattern. We report bizarre nonlinear presentation of Sporotrichosis, in an immunocompetent adult occurring after a visit to Amazon rain forest, speculating infection with more virulent species of Sporothrix. The diagnosis was reached with the help of periodic acid-Schiff positive yeast cells and cigar shaped bodies seen in skin biopsy along with the therapeutic response to potassium iodide.

  14. Chlorine-36 and the initial value problem

    Science.gov (United States)

    Davis, Stanley N.; Cecil, DeWayne; Zreda, Marek; Sharma, Pankaj

    Chlorine-36 is a radionuclide with a half-life of 3.01×105a. Most 36Cl in the hydrosphere originates from cosmic radiation interacting with atmospheric gases. Large amounts were also produced by testing thermonuclear devices during 1952-58. Because the monovalent anion, chloride, is the most common form of chlorine found in the hydrosphere and because it is extremely mobile in aqueous systems, analyses of both total Cl- as well as 36Cl have been important in numerous hydrologic studies. In almost all applications of 36Cl, a knowledge of the initial, or pre-anthropogenic, levels of 36Cl is useful, as well as essential in some cases. Standard approaches to the determination of initial values have been to: (a) calculate the theoretical cosmogenic production and fallout, which varies according to latitude; (b) measure 36Cl in present-day precipitation and assume that anthropogenic components can be neglected; (c) assume that shallow groundwater retains a record of the initial concentration; (d) extract 36Cl from vertical depth profiles in desert soils; (e) recover 36Cl from cores of glacial ice; and (f) calculate subsurface production of 36Cl for water that has been isolated from the atmosphere for more than one million years. The initial value from soil profiles and ice cores is taken as the value that occurs directly below the depth of the easily defined bomb peak. All six methods have serious weaknesses. Complicating factors include 36Cl concentrations not related to cosmogenic sources, changes in cosmogenic production with time, mixed sources of chloride in groundwater, melting and refreezing of water in glaciers, and seasonal groundwater recharge that does not contain average year-long concentrations of 36Cl. Résumé Le chlore-36 est un radionucléide de période 3.01×105a. Pour l'essentiel, le 36Cl dans l'hydrosphère provient des effets du rayonnement cosmique sur les gaz atmosphériques. De grandes quantités de 36Cl ont aussi été produites au cours des

  15. [Electrochemical reduction characteristics and mechanism of chlorinated hydrocarbon at the copper electrode].

    Science.gov (United States)

    Xu, Wen-Ying; Gao, Ting-Yao; Zhou, Rong-Feng; Ma, Lu-Ming

    2005-07-01

    The electrochemical reduction characteristics of chlorinated hydrocarbons were investigated by applying cyclic voltammetry technique. The reduction mechanism and reactivity of the chlorinated hydrocarbons at the copper electrodes were explored. The relation between the reductive reactivity at the copper electrode and the structures of this kind of compounds was discussed. The experimental results show that chlorinated paraffin hydrocarbons and a portion of chlorinated aromatic hydrocarbons could be reduced directly at the copper electrode; however, chlorinated aromatic hydrocarbons aren't easy to reduced directly at the copper electrode. The results provide a theoretical basis for the catalyzed iron inner electrolysis method.

  16. Selective synthesis and characterization of chlorins as sensitizers for photodynamic therapy

    Science.gov (United States)

    Montforts, Franz-Peter; Kusch, Dirk; Hoper, Frank; Braun, Stefan; Gerlach, Benjamin; Brauer, Hans-Dieter; Schermann, Guido; Moser, Joerg G.

    1996-04-01

    Chlorin type sensitizers have ideal photophysical properties for an application in PDT. The basic chlorin framework of these sensitizers has to be modified by attachment of lipophilic and hydrophilic residues to achieve a good cell uptake and tumor enrichment. In the present study we describe the selective synthesis of amphiphilic chlorins starting from the readily accessible red blood pigment heme. The photophysical properties of the well defined synthetic chlorins are characterized by photophysical investigations. The kinetic of cell uptake, the localization in the cell and the photodynamic behavior of the amphiphilic sensitizers are demonstrated by incubation of A 375 cancer cell lines with structurally different chlorins.

  17. Impact of January 2005 solar proton events on chlorine species

    Directory of Open Access Journals (Sweden)

    A. Damiani

    2012-01-01

    Full Text Available Sudden changes in stratospheric chlorine species in the polar northern atmosphere, caused by the Solar Proton Events (SPEs of 17 and 20 January 2005, have been investigated and compared with version 4 of the Whole Atmosphere Community Climate Model (WACCM4. We used Aura Microwave Limb Sounder (MLS measurements to monitor the variability of ClO, HCl, HOCl and Michelson Interferometer for Passive Atmospheric Sounder (MIPAS on ENVISAT to retrieve ClONO2. SPE-induced chlorine activation has been identified. HCl decrease occurred at nearly all the investigated altitudes with the lowest values (of less than 0.25 ppbv on 21 January. HOCl was found to be the main active chlorine species under nighttime conditions (with increases of more than 0.2 ppbv whereas both HOCl and ClO enhancements (about 0.1 ppbv have been observed at the polar night terminator. Further, small ClO decreases (of less than 0.1 ppbv and ClONO2 enhancements (about 0.2 ppbv have been observed at higher latitudes (i.e., at nighttime roughly above 2 hPa.

    While WACCM4 reproduces most of the SPE-induced variability in the chlorine species fairly well, in some particular regions discrepancies between the modeled and measured temporal evolution of the abundances of chlorine species were found. HOCl changes are modelled very well with respect to both magnitude and geographic distribution. ClO decreases are reproduced at high latitudes, whereas ClO enhancements in the terminator region are underestimated and attributed to background variations. WACCM4 also reproduces the HCl depletion in the mesosphere but it does not show the observed decrease below about 2 hPa. Finally, WACCM4 simulations indicate that the observed ClONO2 increase is dominated by background variability, although SPE-induced production might contribute by 0.1 ppbv.

  18. The potential feasibility of chlorinic photosynthesis on exoplanets.

    Science.gov (United States)

    Haas, Johnson R

    2010-11-01

    The modern search for life-bearing exoplanets emphasizes the potential detection of O(2) and O(3) absorption spectra in exoplanetary atmospheres as ideal signatures of biology. However, oxygenic photosynthesis may not arise ubiquitously in exoplanetary biospheres. Alternative evolutionary paths may yield planetary atmospheres tinted with the waste products of other dominant metabolisms, including potentially exotic biochemistries. This paper defines chlorinic photosynthesis (CPS) as biologically mediated photolytic oxidation of aqueous Cl(-) to form halocarbon or dihalogen products, coupled with CO(2) assimilation. This hypothetical metabolism appears to be feasible energetically, physically, and geochemically, and could potentially develop under conditions that approximate the terrestrial Archean. It is hypothesized that an exoplanetary biosphere in which chlorinic photosynthesis dominates primary production would tend to evolve a strongly oxidizing, halogen-enriched atmosphere over geologic time. It is recommended that astronomical observations of exoplanetary outgoing thermal emission spectra consider signs of halogenated chemical species as likely indicators of the presence of a chlorinic biosphere. Planets that favor the evolution of CPS would probably receive equivalent or greater surface UV flux than is produced by the Sun, which would promote stronger abiotic UV photolysis of aqueous halides than occurred during Earth's Archean era and impose stronger evolutionary selection pressures on endemic life to accommodate and utilize halogenated compounds. Ocean-bearing planets of stars with metallicities equivalent to, or greater than, the Sun should especially favor the evolution of chlorinic biospheres because of the higher relative seawater abundances of Cl, Br, and I such planets would tend to host. Directed searches for chlorinic biospheres should probably focus on G0-G2, F, and A spectral class stars that have bulk metallicities of +0.0 Dex or greater.

  19. Degradation mechanisms of geosmin and 2-MIB during UV photolysis and UV/chlorine reactions.

    Science.gov (United States)

    Kim, Tae-Kyoung; Moon, Bo-Ram; Kim, Taeyeon; Kim, Moon-Kyung; Zoh, Kyung-Duk

    2016-11-01

    We conducted chlorination, UV photolysis, and UV/chlorin reactions to investigate the intermediate formation and degradation mechanisms of geosmin and 2-methylisoborneol (2-MIB) in water. Chlorination hardly removed geosmin and 2-MIB, while the UV/chlorine reaction at 254 nm completely removed geosmin and 2-MIB within 40 min and 1 h, respectively, with lesser removals of both compounds during UV photolysis. The kinetics during both UV photolysis and UV/chlorine reactions followed a pseudo first-order reaction. Chloroform was found as a chlorinated intermediate during the UV/chlorine reaction of both geosmin and 2-MIB. The pH affected both the degradation and chloroform production during the UV/chlorine reaction. The open ring and dehydration intermediates identified during UV/chlorine reactions were 1,4-dimethyl-adamantane, and 1,3-dimethyl-adamantane from geosmin, 2-methylenebornane, and 2-methyl-2-bornene from 2-MIB, respectively. Additionally, 2-methyl-3-pentanol, 2,4-dimethyl-1-heptene, 4-methyl-2-heptanone, and 1,1-dichloro-2,4-dimethyl-1-heptane were newly identified intermediates from UV/chlorine reactions of both geosmin and 2-MIB. These intermediates were degraded as the reaction progressed. We proposed possible degradation pathways during the UV photolysis and UV/chlorine reactions of both compounds using the identified intermediates.

  20. Simultaneous Control of Microorganisms and Disinfection By-products by Sequential Chlorination

    Institute of Scientific and Technical Information of China (English)

    CHAO CHEN; XIAO-JIAN ZHANG; WEN-JIE HE; HONG-DA HAN

    2007-01-01

    Objective To introduce a new sequential chlorination disinfection process in which short-term free chlorine and chloramine are sequentially added. Methods Pilot tests of this sequential chlorination were carried out in a drinking water plant. Results The sequential chlorination disinfection process had the same or better efficiency on microbe (including virus)inactivation compared with the free chlorine disinfection process. There seemed to be some synergetic disinfection effect between free chlorine and monochloramine because they attacked different targets. The sequential chlorination disinfection process resulted in 35.7%-77.0% TTHM formation and 36.6%-54.8% THAA5 formation less than the free chlorination process.The poorer the water quality was, the more advantage the sequential chlorination disinfection had over the free chlorination.Conclusion This process takes advantages of free chlorine's quick inactivation of microorganisms and chloramine's low disinfection by-product (DBP) yield and long-term residual effect, allowing simultaneous control of microbes and DBPs in an effective and economic way.

  1. The effect of photochemical dissociation on downwind chlorine dioxide plume concentrations

    Energy Technology Data Exchange (ETDEWEB)

    Michalowicz, R.; Alp, E. [Bovar Environmental, Toronto, Ontario (Canada)

    1997-12-31

    The pulp and paper industry handles toxic gases which may present an inherent hazard to the safety of the general public in the surrounding area. One such toxic gas that may pose a hazard is chlorine dioxide. Spills of chlorine dioxide solution result in the gassing off of toxic clouds of chlorine dioxide. Under daytime dry conditions, chlorine dioxide decomposes photolytically to form chlorine and oxygen and intermediates, chlorine trioxide and chlorine hexoxide. Air dispersion modeling of chlorine dioxide releases which does not properly account for its photochemical decomposition will lead to overly conservative hazard zone estimates. Under these conditions, risk control measures and emergency response evacuation zones based on such estimates will be unnecessarily expensive, perhaps prohibitive. This paper investigates the photolytic rate of dissociation of chlorine dioxide under various atmospheric conditions. It was found that modeling based on the decomposition of chlorine dioxide gas, resulted in downwind distances to TLV-Short Term Exposure Limits which are considerably shorter than modeling based on chlorine dioxide dispersion with no decomposition.

  2. Formation of trichloromethane in chlorinated water and fresh-cut produce and as a result of reacting with citric acid

    Science.gov (United States)

    Chlorine (sodium hypochlorite) is commonly used by the fresh produce industry to sanitize wash water, fresh and fresh-cut fruits and vegetables. However, possible formation of harmful chlorine by-products is a concern. The objectives of this study were to compare chlorine and chlorine dioxide in t...

  3. Reversed flow injection spectrophotometric determination of low residuals of chlorine dioxide in water using chlorophenol red

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    A novel,simple,rapid,sensitive and highly selective flow injection procedure for the spectrophotometrie determination of chlorine dioxide in the presence of other chlorine species,viz,free chlorine,chlorite,chlorate and hypoehlorite,is developed.The method is based on the discoloration reaction between chlorine dioxide and chlorophenol red and can overcome the shortcomings existed in direct speetrophotometrie determination for chlorine dioxide owing to the serious interference of free and combined chlorine.The procedure gave a linear calibration graph over the range 0-0.71 mg/L of chlorine dioxide.With a detection limit of 0.024 mg/L and a sample throughput of 60 samples/h.

  4. Polychlorinated biphenyl toxicity to Japanese quail as related to degree of chlorination

    Science.gov (United States)

    Hill, E.F.; Heath, R.G.; Spann, J.W.; Williams, J.D.

    1974-01-01

    To learn if the percentage of chlorine in a mixture of polychlorinated biphenyls (PCB's) alone determines toxicity, Japanese quail were fed diets containing Aroelor 1248, 1254, or 1260 at levels that added equal amounts of chlorine to the feed. The experiment comprised two consecutive 5-day periods; three sublethal concentrations of chlorine were evaluated during the first period and three lethal concentrations during the second period. Evaluations utilized comparisons of mortality, time to death, weight change, and food consumption. Sublethal concentrations produced no detectable effects. Lethal concentrations with equal Chlorine showed Aroelor 1248 to be less toxic at the highest chlorine concentrations, but at lower concentrations Aroelor 1254 was more toxic than Aroclor 1260. Although chlorine percentage of a PCB is positively correlated with its avian toxicity, PCB toxicity is apparently not simply a function of chlorination.

  5. Direct chlorination process for geothermal power plant off-gas - hydrogen sulfide abatement

    Energy Technology Data Exchange (ETDEWEB)

    Sims, A.V.

    1983-06-01

    The Direct Chlorination Process removes hydrogen sulfide from geothermal off-gases by reacting hydrogen sulfide with chlorine in the gas phase. Hydrogen chloride and elemental sulfur are formed by this reaction. The Direct Chlorination Process has been successfully demonstrated by an on-site operation of a pilot plant at the 3 M We HPG-A geothermal power plant in the Puna District on the island of Hawaii. Over 99.5 percent hydrogen sulfide removal was achieved in a single reaction state. Chlorine gas did not escape the pilot plant, even when 90 percent excess chlorine gas was used. A preliminary economic evaluation of the Direct Chlorination Process indicates that it is very competitive with the Stretford Process. Compared to the Stretford Process, the Direct Chlorination Process requires about one-third the initial capital investment and about one-fourth the net daily expenditure.

  6. Fate of chlorinated fatty acids in migrating sockeye salmon and their transfer to arctic grayling

    DEFF Research Database (Denmark)

    Mu, Huiling; Ewald, G.; Nilsson, E.;

    2004-01-01

    organohalogen compounds in the salmon were halogenated fatty acids, predominantly chlorinated species that accounted for up to 35% of the extractable, organically bound chlorine (EOCl) in the fish tissues. The amount of chlorinated fatty acids in the salmon muscle decreased as a result of spawning migration....... The decrease was correlated with that of triacylglycerols in the salmon muscle, indicating the chlorinated fatty acids to be mobilized and metabolized to approximately the same extent as the other fatty acids. Chlorinated fatty acids were also transferred to the maturing roe in a manner similar...... to that of the unchlorinated fatty acids. Lipids of the Arctic grayling (Thymallus arcticus), a fish resident to the spawning lake of the salmon, contained higher concentrations of chlorinated fatty acids than grayling in a lake without migratory salmon. This may reflect a food-chain transfer of the chlorinated fatty acids...

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

    Science.gov (United States)

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

  8. Mutagenic activity associated with by-products of drinking water disinfection by chlorine, chlorine dioxide, ozone and UV-irradiation.

    Science.gov (United States)

    Zoeteman, B C; Hrubec, J; de Greef, E; Kool, H J

    1982-12-01

    A retrospective epidemiological study in The Netherlands showed a statistical association between chlorination by-products in drinking water and cancer of the esophagus and stomach for males. A pilot-plant study with alternative disinfectants was carried out with stored water of the Rivers Rhine and Meuse. It was demonstrated that the increase of direct acting mutagens after treatment with chlorine dioxide is similar to the effect of chlorination. Ozonation of Rhine water reduced the mutagenic activity for Salmonella typhimurium TA 98 both with and without metabolic activation. UV alone hardly affects the mutagenicity of the stored river water for S. typh. TA 98. In all studies, practically no mutagenic activity for S. typh. TA 100 was found. Although remarkable changes in the concentration of individual organic compounds are reported, the identity of the mutagens detected is yet unclear. Compounds of possible interest due to their removal by ozonation are 1,3,3-trimethyloxindole, dicyclopentadiene and several alkylquinolines. Compounds which might be responsible for the increased mutagenicity after chlorination are two brominated acetonitriles and tri(2-chlorethyl) phosphate. Furthermore, the concentration procedure with adsorption on XAD resin and the subsequent elution step may have affected the results. It is proposed to focus further research more on the less volatile by-products of disinfection than on the trihalomethanes.

  9. Zinc iodide-osmium staining of membrane-coating granules in keratinized and non-keratinized mammalian oral epithelium.

    Science.gov (United States)

    Squier, C A

    1982-01-01

    Specimens of keratinized and non-keratinized oral epithelium were examined in the electron microscope after being stained with zinc iodide-osmium. In both types of tissue, reaction was seen in unmyelinated nerves, in the specific granules of epithelial Langerhans cells and within lysosome-like organelles and small vesicles associated with Golgi systems. In keratinized epithelia, the reaction was also present in the membrane-coating granules and between the deepest cells of the keratinized layer. In contrast, the membrane-coating granules of non-keratinized epithelia lacked Zn iodide-osmium staining despite the presence of reaction in adjacent Golgi systems. It is suggested that Zn iodide-osmium stains glycolipid or glycoprotein material in the cell. This material is elaborated in the Golgi systems from which lysosomes and the membrane-coating granules of keratinized tissues are probably derived.

  10. Colorimetric Solid Phase Extraction for the Measurement of Total I (Iodine, Iodide, and Triiodide) in Spacecraft Drinking Water

    Science.gov (United States)

    Lipert, Robert J.; Porter, Marc D.; Siperko, Lorraine M.; Gazda, Daniel B.; Rutz, Jeff A.; Schultz, John R.; Carrizales, Stephanie M.; McCoy, J. Torin

    2009-01-01

    An experimental drinking water monitoring kit for the measurement of iodine and silver(I) was recently delivered to the International Space Station (ISS). The kit is based on Colorimetric Solid Phase Extraction (CSPE) technology, which measures the change in diffuse reflectance of indicator disks following exposure to a water sample. To satisfy additional spacecraft water monitoring requirements, CSPE has now been extended to encompass the measurement of total I (iodine, iodide, and triiodide) through the introduction of an oxidizing agent, which converts iodide and triiodide to iodine, for measurement using the same indicator disks currently being tested on ISS. These disks detect iodine, but are insensitive to iodide and triiodide. We report here the operational considerations, design, and ground-based performance of the CSPE method for total I. The results demonstrate that CSPE technology is poised to meet NASA's total I monitoring requirements.

  11. Bio-inspired stabilization of sulfenyl iodide RS-I in a Zr(IV)-based metal-organic framework.

    Science.gov (United States)

    Yee, Ka-Kit; Wong, Yan-Lung; Xu, Zhengtao

    2016-03-28

    A Zr(IV)-based metal-organic framework (MOF) appended with free-standing thiol (-SH) groups was found to react readily with I2 molecules to form sulfenyl iodide (S-I) units. In contrast to its solution chemistry of facile disproportionation into disulfide and I2, the sulfenyl iodide (SI) function, anchored onto the rigid MOF grid and thus prevented from approaching one another to undergo the dismutation reaction, exhibits distinct stability even at elevated temperatures (e.g., 90 °C). On a conceptual plane, this simple and effective solid host also captures the spatial confinement observed for the complex biomacromolecular scaffolds involved in iodine thyroid chemistry, wherein the spatial isolation and consequent stabilization of sulfenyl/selenenyl iodides are exerted by means of the protein scaffolds.

  12. Synthesis of 1-/sup 11/C-labelled ethyl, propyl, butyl and isobutyl iodides and examples of alkylation reactions

    Energy Technology Data Exchange (ETDEWEB)

    Laangstroem, B.; Antoni, G.; Gullberg, P.; Halldin, C.; Naagren, K.; Rimland, A.; Svaerd, H.

    1986-01-01

    New /sup 11/C-labelled precursors (1-/sup 11/C)ethyl,(1-/sup 11/C)propyl, (1-/sup 11/C)butyl, and (1-/sup 11/C)isobutyl iodides have been prepared by a 3-step reaction route using a one-pot system. The labelled iodides were obtained in 20-55% radiochemical yields and 65-95% radiochemical purities, with a total time for synthesis of the order of 10-14 min. The labelled iodides have been used in alkylation reactions with nitrogen, oxygen and carbon nucleophiles. The nitrogen alkylation reactions are exemplified by the synthesis of the analgetics N-(1-/sup 11/C-ethyl)iodocaine and N-(1-/sup 11/C-butyl) bupivacaine. The synthesis of 3-nitrophenyl(1-/sup 11/C)propyl ether is also presented in this paper as an example of an oxygen alkylation.

  13. Heat capacity and density of potassium iodide solutions in mixed N-methylpyrrolidone-water solvent at 298.15 K

    Science.gov (United States)

    Novikov, A. N.

    2014-10-01

    The heat capacity and density of potassium iodide solutions in a mixed N-methylpyrrolidone (MP)-water solvent with a low content of the organic component are measured via calorimetry and densimetry at 298.15 K. Standard partial molal heat capacities and volumes of potassium iodide in MP-water mixtures are calculated. Standard heat capacities and volumes of potassium and iodide ions are determined. The character of the changes in heat capacity and volume are discussed on the basis of calculating additivity coefficients δ c and δ v upon the mixing of isomolal binary solutions KI-MP and KI-water, depending on the composition of the MP-H2O mixture and the concentration of the electrolyte.

  14. Phase diagram of an iodine-potassium iodide-water-ethanol system at 25°C

    Science.gov (United States)

    Varlamova, T. M.; Rubtsova, E. M.; Mushtakova, S. P.

    2012-09-01

    Phase equilibriums are studied in the isothermal-isobaric sections of the phase diagram of a fourcomponent iodine-potassium iodide-water-ethanol system at 25°C and atmospheric pressure. The compositions of the solvent at which it exhibits the greatest ability to dissolve iodine are established. It is shown that in all the investigated sections, there is three-phase eutonic equilibrium with potassium iodide and crystalline iodine as the solid phases. It is revealed that in the sections containing 30 and 50% of ethanol, potassium iodide serves as the salting in agent for crystalline iodine, due to the formation of polyiodide complexes of various composition in the studied system.

  15. Analysis of heterogeneous water vapor uptake by metal iodide cluster ions via differential mobility analysis-mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Oberreit, Derek [Department of Mechanical Engineering, University of Minnesota, Minneapolis, Minnesota 55455 (United States); Fluid Measurement Technologies, Inc., Saint Paul, Minnesota 55110 (United States); Rawat, Vivek K.; Larriba-Andaluz, Carlos; Ouyang, Hui; McMurry, Peter H.; Hogan, Christopher J., E-mail: hogan108@umn.edu [Department of Mechanical Engineering, University of Minnesota, Minneapolis, Minnesota 55455 (United States)

    2015-09-14

    The sorption of vapor molecules onto pre-existing nanometer sized clusters is of importance in understanding particle formation and growth in gas phase environments and devising gas phase separation schemes. Here, we apply a differential mobility analyzer-mass spectrometer based approach to observe directly the sorption of vapor molecules onto iodide cluster ions of the form (MI){sub x}M{sup +} (x = 1-13, M = Na, K, Rb, or Cs) in air at 300 K and with water saturation ratios in the 0.01-0.64 range. The extent of vapor sorption is quantified in measurements by the shift in collision cross section (CCS) for each ion. We find that CCS measurements are sensitive enough to detect the transient binding of several vapor molecules to clusters, which shift CCSs by only several percent. At the same time, for the highest saturation ratios examined, we observed CCS shifts of up to 45%. For x < 4, cesium, rubidium, and potassium iodide cluster ions are found to uptake water to a similar extent, while sodium iodide clusters uptake less water. For x ≥ 4, sodium iodide cluster ions uptake proportionally more water vapor than rubidium and potassium iodide cluster ions, while cesium iodide ions exhibit less uptake. Measured CCS shifts are compared to predictions based upon a Kelvin-Thomson-Raoult (KTR) model as well as a Langmuir adsorption model. We find that the Langmuir adsorption model can be fit well to measurements. Meanwhile, KTR predictions deviate from measurements, which suggests that the earliest stages of vapor uptake by nanometer scale species are not well described by the KTR model.

  16. Analysis of perchlorate, thiocyanate, nitrate and iodide in human amniotic fluid using ion chromatography and electrospray tandem mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Blount, Benjamin C. [Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA 30341 (United States)]. E-mail: bblount@cdc.gov; Valentin-Blasini, Liza [Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA 30341 (United States)

    2006-05-10

    Because of health concerns surrounding in utero exposure to perchlorate, we developed a sensitive and selective method for quantifying iodide, as well as perchlorate and other sodium-iodide symporter (NIS) inhibitors in human amniotic fluid using ion chromatography coupled with electrospray ionization tandem mass spectrometry. Iodide and NIS inhibitors were quantified using a stable isotope-labeled internal standards (Cl{sup 18}O{sub 4} {sup -}, S{sup 13}CN{sup -} and {sup 15}NO{sub 3} {sup -} with excellent assay accuracy of 100%, 98%, 99%, 95% for perchlorate, thiocyanate, nitrate and iodide, respectively, in triplicate analysis of spiked amniotic fluid sample). Excellent analytical precision (<5.2% RSD for all analytes) was found when amniotic fluid quality control pools were repetitively analyzed for iodide and NIS-inhibitors. Selective chromatography and tandem mass spectrometry reduced the need for sample cleanup, resulting in a rugged and rapid method capable of routinely analyzing 75 samples/day. Analytical response was linear across the physiologically relevant concentration range for the analytes. Analysis of a set of 48 amniotic fluid samples identified the range and median levels for perchlorate (0.057-0.71, 0.18 {mu}g/L), thiocyanate (<10-5860, 89 {mu}g/L), nitrate (650-8900, 1620 {mu}g/L) and iodide (1.7-170, 8.1 {mu}g/L). This selective, sensitive, and rapid method will help assess exposure of the developing fetus to low levels of NIS-inhibitors and their potential to inhibit thyroid function.

  17. Formation of organic iodine supplied as iodide in a soil-water system in Chiba, Japan.

    Science.gov (United States)

    Shimamoto, Yoko S; Takahashi, Yoshio; Terada, Yasuko

    2011-03-15

    Speciation of iodine in a soil-water system was investigated to understand the mechanism of iodine mobility in surface environments. Iodine speciation in soil and pore water was determined by K-edge XANES and HPLC-ICP-MS, respectively, for samples collected at a depth of 0-12 cm in the Yoro area, Chiba, Japan. Pore water collected at a 0-6 cm depth contained 50%-60% of organic iodine bound to dissolved organic matter, with the other portion being I(-). At a 9-12 cm depth, 98% of iodine was in the form of dissolved I(-). In contrast, XANES analysis revealed that iodine in soil exists as organic iodine at all depths. Iodine mapping of soil grains was obtained using micro-XRF analysis, which also indicated that iodine is bound to organic matter. The activity of laccase, which has the ability to oxidize I(-) to I(2), was high at the surface of the soil-water layer, suggesting that iodide oxidizing enzymes can promote iodine organification. The distribution coefficient of organic iodine in the soil-water system was more than 10-fold greater than that of iodide. Transformation of inorganic iodine to organic iodine plays an important role in iodine immobilization, especially in a surface soil-water system.

  18. Photocatalytic hydrogen generation from hydriodic acid using methylammonium lead iodide in dynamic equilibrium with aqueous solution

    Science.gov (United States)

    Park, Sunghak; Chang, Woo Je; Lee, Chan Woo; Park, Sangbaek; Ahn, Hyo-Yong; Nam, Ki Tae

    2017-01-01

    The solar-driven splitting of hydrohalic acids (HX) is an important and fast growing research direction for H2 production. In addition to the hydrogen, the resulting chemicals (X2/X3-) can be used to propagate a continuous process in a closed cycle and are themselves useful products. Here we present a strategy for photocatalytic hydrogen iodide (HI) splitting using methylammonium lead iodide (MAPbI3) in an effort to develop a cost-effective and easily scalable process. Considering that MAPbI3 is a water-soluble ionic compound, we exploit the dynamic equilibrium of the dissolution and precipitation of MAPbI3 in saturated aqueous solutions. The I- and H+ concentrations of the aqueous solution are determined to be the critical parameters for the stabilization of the tetragonal MAPbI3 phase. Stable and efficient H2 production under visible light irradiation was demonstrated. The solar HI splitting efficiency of MAPbI3 was 0.81% when using Pt as a cocatalyst.

  19. Inhibition of acid corrosion of steel by some S-alkylisothiouronium iodides

    Energy Technology Data Exchange (ETDEWEB)

    Arab, S.T.; Noor, E.A. (Girl' s Coll. of Education, Jeddah (Saudi Arabia))

    1993-02-01

    Five selected S-alkylisothisothiouronium iodides have been studied as acid corrosion inhibitors at 30 C for steel in 0.5 M H[sub 2]SO[sub 4] using gasometry, mass loss, and direct current (DC) polarization techniques. All of the data reveal that the compounds act as inhibitors in the acid environments; furthermore, polarization curves show that the compounds act as mixed-type inhibitors. It was found that the inhibition efficiency increases with the increase of the length of the additive alkyl chain. Langmuir's adsorption isotherms fit the experimental data for the studied compounds. Thermodynamic parameter were obtained from experimental data of the temperature studies of the inhibition process at five temperatures ranging from 30 to 70 C. It was observed that the activation energy is slightly increased with the increase of the additive alkyl chain. On the other hand, the sudden large increase of the inhibition behavior of S-hexylisothiouronium iodide was attributed to a different adsorption process.

  20. Sodium Iodide Symporter for Nuclear Molecular Imaging and Gene Therapy: From Bedside to Bench and Back

    Directory of Open Access Journals (Sweden)

    Byeong-Cheol Ahn

    2012-01-01

    Full Text Available Molecular imaging, defined as the visual representation, characterization and quantification of biological processes at the cellular and subcellular levels within intact living organisms, can be obtained by various imaging technologies, including nuclear imaging methods. Imaging of normal thyroid tissue and differentiated thyroid cancer, and treatment of thyroid cancer with radioiodine rely on the expression of the sodium iodide symporter (NIS in these cells. NIS is an intrinsic membrane protein with 13 transmembrane domains and it takes up iodide into the cytosol from the extracellular fluid. By transferring NIS function to various cells via gene transfer, the cells can be visualized with gamma or positron emitting radioisotopes such as Tc-99m, I-123, I-131, I-124 and F-18 tetrafluoroborate, which are accumulated by NIS. They can also be treated with beta- or alpha-emitting radionuclides, such as I-131, Re-186, Re-188 and At-211, which are also accumulated by NIS. This article demonstrates the diagnostic and therapeutic applications of NIS as a radionuclide-based reporter gene for trafficking cells and a therapeutic gene for treating cancers.

  1. Chitosan finishing nonwoven textiles loaded with silver and iodide for antibacterial wound dressing applications.

    Science.gov (United States)

    Aubert-Viard, François; Martin, Adeline; Chai, Feng; Neut, Christel; Tabary, Nicolas; Martel, Bernard; Blanchemain, Nicolas

    2015-03-02

    Polyethylene terephtalate (PET) and Polypropylene (PP) textiles are widely used in biomedical application such as wound dressings and implants. The aim of this work was to develop an antibacterial chitosan (CHT) coating activated by silver or by iodine. Chitosan was immobilized onto PET and PP supports using citric acid (CTR) as a crosslinking agent through a pad-dry-cure textile finishing process. Interestingly, depending on the CHT/CTR molar ratio, two different systems were obtained: rich in cationic ammonium groups when the CTR concentration was 1%w/v, and rich in anionic carboxylate groups when the CTR concentration was 10%w/v. As a consequence, such samples could be selectively loaded with iodine and silver nitrate, respectively.Both types of coatings were analyzed using SEM and FTIR, their sorption capacities were evaluated toward iodide/iodate anions (I(-)/IO3(-)) and the silver cations (Ag(+)) were evaluated using elemental analysis. Finally, in vitro evaluations were carried out to evaluate the cytocompatibility on the epithelial cell line. The silver loaded textile reported a stronger antibacterial effect against E.coli (5 log10 reduction) than toward S. aureus (3 log10) while the antibacterial effect of the iodide loaded textiles was limited to 1 log10 to 2 log10 on both strains.

  2. The effect of potassium iodide on the production of acid phosphatase by Sporothrix schenckii

    Directory of Open Access Journals (Sweden)

    P. S. Grover

    2003-06-01

    Full Text Available The present study was undertaken to find out the in vitro effect of potassium iodide (KI on the production of acid phosphatase by fully characterized strain of S.schenckii isolated from a patient of Cutaneous Sporotrichosis. The enzyme acid phosphatase was estimated during the 3 phases of growth of S.schenckii, without and with three concentrations of KI incorporated in the culture medium. In the control and in the test proper, with various concentrations of KI, no adverse effect of KI was observed on the production of acid phosphatase in early and mid log phase of fungal growth. Whereas in the exponential phase in test proper, there was a statistical significant decrease in the enzyme production with 0.8% and 3.2% of KI. The low activity at 0.8% and 3.2% KI indicates that KI has inhibitory effect on the growth of S.schenckii and has led to decrease in the activity of the enzyme. (Med J Indones 2003; 12: 65-8 Keywords: S.schenckii, acid phosphatase, potassium iodide

  3. Serum and tissue iodine concentrations in rats fed diets supplemented with kombu powder or potassium iodide.

    Science.gov (United States)

    Yoshida, Munehiro; Mukama, Ayumi; Hosomi, Ryota; Fukunaga, Kenji; Nishiyama, Toshimasa

    2014-01-01

    Serum and tissue iodine concentration was measured in rats fed a diet supplemented with powdered kombu (Saccharina sculpera) or potassium iodide to evaluate the absorption of iodine from kombu. Eighteen male 5-wk-old Wistar rats were divided into three groups and fed a basal AIN93G diet (iodine content, 0.2 mg/kg) or the basal diet supplemented with iodine (183 mg/kg) either in the form of kombu powder or potassium iodine (KI) for 4 wk. There were no differences in weight gain or serum biochemistry tests (alanine aminotransferase and aspartate aminotransferase activity, and total serum cholesterol and triglyceride concentration) after iodine supplementation. In addition, serum levels of the thyroid hormones thyroxine and triiodothyronine, as well as thyroid-stimulating hormone, were not affected. On the other hand, serum and tissue (thyroid, liver and kidney) iodine concentrations were markedly elevated after iodine supplementation. There was no difference in thyroid iodine concentration between KI and kombu supplementation. However, there was a significant difference observed in the iodine concentrations of serum, liver and kidney between the two iodine sources; rats fed KI had iodine concentrations in these tissues 1.8 to 1.9 times higher than those in rats fed kombu powder. These results suggest that the absorption of iodine from kombu is reduced compared to that from potassium iodide.

  4. Toxicity of tetramethylammonium hydroxide to aquatic organisms and its synergistic action with potassium iodide.

    Science.gov (United States)

    Mori, Izumi C; Arias-Barreiro, Carlos R; Koutsaftis, Apostolos; Ogo, Atsushi; Kawano, Tomonori; Yoshizuka, Kazuharu; Inayat-Hussain, Salmaan H; Aoyama, Isao

    2015-02-01

    The aquatic ecotoxicity of chemicals involved in the manufacturing process of thin film transistor liquid crystal displays was assessed with a battery of four selected acute toxicity bioassays. We focused on tetramethylammonium hydroxide (TMAH, CAS No. 75-59-2), a widely utilized etchant. The toxicity of TMAH was low when tested in the 72 h-algal growth inhibition test (Pseudokirchneriellia subcapitata, EC50=360 mg L(-1)) and the Microtox® test (Vibrio fischeri, IC50=6.4 g L(-1)). In contrast, the 24h-microcrustacean immobilization and the 96 h-fish mortality tests showed relatively higher toxicity (Daphnia magna, EC50=32 mg L(-1) and Oryzias latipes, LC50=154 mg L(-1)). Isobologram and mixture toxicity index analyses revealed apparent synergism of the mixture of TMAH and potassium iodide when examined with the D. magna immobilization test. The synergistic action was unique to iodide over other halide salts i.e. fluoride, chloride and bromide. Quaternary ammonium ions with longer alkyl chains such as tetraethylammonium and tetrabutylammonium were more toxic than TMAH in the D. magna immobilization test.

  5. Iodine in raw and pasteurized milk of dairy cows fed different amounts of potassium iodide.

    Science.gov (United States)

    Norouzian, M A

    2011-02-01

    Relation between iodine (I) intake by lactating Holstein cows and iodine concentrations in raw and pasteurized milk were investigated. Four treatment groups with eight cows assigned to each treatment were fed a basal diet containing 0.534 mg I/kg alone or supplemented with potassium iodide at 2.5, 5 or 7.5 mg/kg in 7-week period. Iodine concentrations in raw milk increased with each increase in dietary I from 162.2 ng/ml for basal diet to 534.5, 559.8 and 607.5 ng/ml when 2.5, 5 and 7.5 mg/kg was fed as potassium iodide (P < 0.05). This trend was found for blood plasma and urine iodine concentration. Iodine supplementation had no significant effect on thyroidal hormones. high-temperature short-time (HTST) pasteurization process reduced I concentration. The mean iodine content found in the milk prior to heating processing was 466.0 ± 205.0 ng/ml, whereas for the processed milk this level was 349.5 ± 172.8 ng/ml. It was concluded that iodine supplementation above of NRC recommendation (0.5 mg/kg diet DM) resulted in significant increases in iodine concentrations in milk, although the effect of heating in HTST pasteurization process on iodine concentration was not negligible.

  6. Characterization of thermally evaporated lead iodide films aimed for the detection of X-rays

    Energy Technology Data Exchange (ETDEWEB)

    Caldeira Filho, A.M. [Departamento de Fisica, Faculdade de Filosofia, Ciencias e Letras de Ribeirao Preto, Universidade de Sao Paulo - USP, Avenida Bandeirantes 3900, 14040-901, Ribeirao Preto-SP (Brazil); Mulato, M., E-mail: mmulato@ffclrp.usp.b [Departamento de Fisica, Faculdade de Filosofia, Ciencias e Letras de Ribeirao Preto, Universidade de Sao Paulo - USP, Avenida Bandeirantes 3900, 14040-901, Ribeirao Preto-SP (Brazil)

    2011-04-21

    Some semiconductor materials such as lead iodide (PbI{sub 2}) have applications in the detection of ionizing radiation at room temperature using the direct detection method. In this work we investigate lead iodide films deposited by thermal evaporation. The morphology, structure, and electric properties were investigated as a function of deposition height, i.e. the distance between evaporation-boat and substrates. The results show a morphology of vertical leaves and X-ray diffraction shows just one preferential orientation along the direction 110. Energy dispersive spectroscopy reveals that the films are not stoichiometric, with excess iodine atoms. Electrical resistivity of about 10{sup 8} {Omega} cm was measured. This is smaller than for the bulk due to structural defects. The values of activation energy for electric transport increase from 0.52 up to 1.1 eV with decreasing deposition height, what indicates that the best film is the one deposited at the shortest distance. Exposure under X-ray mammographic energy shows a linear behavior up to 500 mR. No variation in sensibility was observed between 22 and 30 kVp.

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

    Science.gov (United States)

    Yang, Xin; Guo, Wanhong; Lee, Wontae

    2013-06-01

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

  8. Durability of Selected Membrane Materials when Exposed to Chlorine Gas

    Energy Technology Data Exchange (ETDEWEB)

    Eikeland, Marianne Soerflaten

    2001-03-01

    This thesis is focusing on the durability of selected membrane materials when exposed to chlorine gas in the temperature range 30-100{sup o}C. Studies of the changes of membrane separation properties and the mechanisms promoting these changes have been studied. The selected membrane materials were poly(dimethylsioxane) (PDMS), Fluorel, fluorosilicone, and blends of PDMS and Fluorel. The thesis is organised in seven chapters. The first chapter gives an introduction to the background of the work. The second chapter presents the theory for gas separation using dense rubbery membranes. The properties of the selected membrane materials are presented in chapter three. The fourth chapter describes degradation mechanisms for polymeric materials in general and for the selected membrane materials in particular. Presentation of the experimental work is given in chapter five, while the results with discussions are presented in chapter six. The conclusions and recommendations for further studies are given in chapter seven. Five appendixes are attached: Appendix A describes the calculations of permeability and solubility coefficients and the accuracy of the experimental measurements. Appendix B summarises the measured values in tables and Appendix C describes the analytical methods. Appendix D gives the properties of the gases used in the experiments. Appendix E is the article ''Durability of Poly(dimethylsiloxane) when Exposed to Chlorine Gas'', submitted to the Journal of Applied Polymer Science. Highly crosslinked PDMS was found to have an initial high permeability for chlorine gas and a high Cl{sub 2}/O{sub 2} selectivity. However when exposed to chlorine gas the permeability decreased significantly. Crosslinking of the PDMS polymer chain and chlorination of the polymer gave a denser polymer structure and thus lower permeability. Fluorel showed very low permeabilities and selectivities for the gases in question and was thus not interesting for this

  9. Administration of additional inactive iodide during radioiodine therapy for Graves' disease. Who might benefit?

    Energy Technology Data Exchange (ETDEWEB)

    Dietlein, M.; Moka, D.; Reinholz, U.; Schmidt, M.; Schomaecker, K.; Schicha, H.; Wellner, U. [Koeln Univ. (Germany). Dept. of Nuclear Medicine

    2007-07-01

    Aim: Graves' hyperthyroidism and antithyroid drugs empty the intrathyroid stores of hormones and iodine. The consequence is rapid {sup 131}I turnover and impending failure of radioiodine therapy. Can administration of additional inactive iodide improve 131I kinetics? Patients, methods: Fifteen consecutive patients, in whom the 48 h post-therapeutically calculated thyroid dose was between 150 and 249 Gy due to an unexpectedly short half-life, received 3 x 200 {mu}g inactive potassium-iodide ({sup 127}I) daily for 3 days (Group A), while 17 consecutive patients with a thyroid dose of = 250 Gy (Group B) served as the non-iodide group. 48 hours after {sup 131}I administration (M1) and 4 or 5 days later (M2) the following parameters were compared: effective {sup 131}I half-life, thyroid dose, total T3, total T4, {sup 131}I-activity in the T3- and T4-RIAs. Results: In Group A, the effective {sup 131}I half-life M1 before iodine (3.81 {+-} 0.93 days) was significantly (p <0.01) shorter than the effective {sup 131}I half-life M2 (4.65 {+-} 0.79 days). Effective {sup 131}I half-life M1 correlated with the benefit from inactive {sup 127}I (r = -0.79): Administration of {sup 127}I was beneficial in patients with an effective {sup 131}I half-life M1 of <3 or 4 days. Patients from Group A with high initial specific {sup 131}I activity of T3 and T4 showed lower specific {sup 131}I activity after addition of inactive iodine compared with patients from the same group with a lower initial specific {sup 131}I activity of T3 and T4 and compared with the patient group B who was given no additional inactive iodide. This correlation was mathematically described and reflected in the flatter gradient in Group A (y = 0.5195x + 0.8727 for {sup 131}I T3 and y = 1.0827x - 0.4444 for {sup 131}I T4) and steeper gradient for Group B (y = 0.6998x + 0.5417 for {sup 131}I T3 and y = 1.3191x - 0.2901 for {sup 131}I T4). Radioiodine therapy was successful in all 15 patients from Group A

  10. Replacement of monochromator and proportional gas counter by mercuric iodide detector in X-ray powder diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Nissenbaum, J.; Levi, A.; Burger, A.; Schieber, M. (Hebrew Univ., Jerusalem (Israel). School of Applied Science and Technology)

    1983-02-01

    Low resolution and therefore low-cost mercuric iodide detectors have successfully been applied to replace the combination of a graphite monochromator and a proportional gas radiation counter used in X-ray diffractometers. The mercuric iodide detector requires a lower DC bias of only 200 V rather than the 1500 V bias needed for the proportional gas counter. The much better stopping power of HgI/sub 2/ allows higher counting efficiency and therefore a better signal-to-noise ratio. Results are shown for X-ray powder diffractions of polycrystalline cubic silicon and tetragonal HgI/sub 2/.

  11. Inner Sphere and Outer Sphere Electron Transfer to Methyl Iodide. Deuterium and 13C Kinetic Isotope Effects

    DEFF Research Database (Denmark)

    Holm, Torkil; Crossland, Ingolf

    1996-01-01

    Deuterium and 13C kinetic isotope effects (KIEs) have been determined for the conversion of methyl iodide into methyl radical via inner sphere ET (electron transfer) and via outer sphere ET. The alfa-deuterium KIE was found to be very high for in......Deuterium and 13C kinetic isotope effects (KIEs) have been determined for the conversion of methyl iodide into methyl radical via inner sphere ET (electron transfer) and via outer sphere ET. The alfa-deuterium KIE was found to be very high for in...

  12. Impact of UV/H2O2 pre-oxidation on the formation of haloacetamides and other nitrogenous disinfection byproducts during chlorination.

    Science.gov (United States)

    Chu, Wenhai; Gao, Naiyun; Yin, Daqiang; Krasner, Stuart W; Mitch, William A

    2014-10-21

    Haloacetamides (HAcAms), an emerging class of nitrogen-based disinfection byproducts (N-DBPs) of health concern in drinking water, have been found in drinking waters at μg/L levels. However, there is a limited understanding about the formation, speciation, and control of halogenated HAcAms. Higher ultraviolet (UV) doses and UV advanced oxidation (UV/H2O2) processes (AOPs) are under consideration for the treatment of trace organic pollutants. The objective of this study was to examine the potential of pretreatment with UV irradiation, H2O2 oxidation, and a UV/H2O2 AOP for minimizing the formation of HAcAms, as well as other emerging N-DBPs, during postchlorination. We investigated changes in HAcAm formation and speciation attributed to UV, H2O2 or UV/H2O2 followed by the application of free chlorine to quench any excess hydrogen peroxide and to provide residual disinfection. The results showed that low-pressure UV irradiation alone (19.5-585 mJ/cm(2)) and H2O2 preoxidation alone (2-20 mg/L) did not significantly change total HAcAm formation during subsequent chlorination. However, H2O2 preoxidation alone resulted in diiodoacetamide formation in two iodide-containing waters and increased bromine utilization. Alternatively, UV/H2O2 preoxidation using UV (585 mJ/cm(2)) and H2O2 (10 mg/L) doses typically employed for trace contaminant removal controlled the formation of HAcAms and several other N-DBPs in drinking water.

  13. Chlorine isotope behavior during prograde metamorphism of sedimentary rocks

    Science.gov (United States)

    Selverstone, Jane; Sharp, Zachary D.

    2015-05-01

    Chlorine stable isotope compositions of two sedimentary sequences and their metamorphic equivalents were measured in order to study fractionation effects during prograde metamorphism and devolatilization. Protoliths (n = 25) were collected from a 50 m section of Triassic fluvial and playa-lake strata and Jurassic (Liassic) marine black shales in a well-characterized quarry. Low greenschist to middle amphibolite facies equivalents (n > 80) were collected from the Glarus Alps, Urseren Zone, and Lucomagno region. Bulk δ37Cl values are constant within individual sedimentary layers, but vary from -2.0 to + 2.4 ‰ in Triassic rocks and from -3.0 to 0‰ in the black shales. Dolomitic and gypsiferous samples have positive δ37Cl values, but marls and shales are isotopically negative. Bulk Cl contents show only small declines during the earliest stages of metamorphism. Metamorphic equivalents of the Triassic and Liassic protoliths record the same overall ranges in δ37Cl as their protoliths. Samples with highly correlated bulk compositions but different metamorphic grade show no statistically significant difference in δ37Cl. These data lead to the following conclusions: (1) Terrestrial and marine sedimentary rocks display large primary heterogeneities in chlorine isotope composition. As a result, an unambiguous "sedimentary signature" does not exist in the chlorine stable isotope system. (2) No isotopic fractionation is discernable during metamorphic devolatilization, even at low temperatures. Alpine-style metamorphism thus has little to no effect on bulk chlorine isotopic compositions, despite significant devolatilization. (3) Cl is largely retained in the rocks during devolatilization, contrary to the normally assumed hydrophilic behavior of chlorine. Continuous release of mixed-volatile C-O-H fluids likely affected Cl partitioning between fluid and minerals and allowed chlorine to remain in the rocks. (4) There is no evidence for fluid communication across (meta

  14. Constraining the sensitivity of iodide adduct chemical ionization mass spectrometry to multifunctional organic molecules using the collision limit and thermodynamic stability of iodide ion adducts

    Science.gov (United States)

    Lopez-Hilfiker, Felipe D.; Iyer, Siddarth; Mohr, Claudia; Lee, Ben H.; D'Ambro, Emma L.; Kurtén, Theo; Thornton, Joel A.

    2016-04-01

    The sensitivity of a chemical ionization mass spectrometer (ions formed per number density of analytes) is fundamentally limited by the collision frequency between reagent ions and analytes, known as the collision limit, the ion-molecule reaction time, and the transmission efficiency of product ions to the detector. We use the response of a time-of-flight chemical ionization mass spectrometer (ToF-CIMS) to N2O5, known to react with iodide at the collision limit, to constrain the combined effects of ion-molecule reaction time, which is strongly influenced by mixing and ion losses in the ion-molecule reaction drift tube. A mass spectrometric voltage scanning procedure elucidates the relative binding energies of the ion adducts, which influence the transmission efficiency of molecular ions through the electric fields within the vacuum chamber. Together, this information provides a critical constraint on the sensitivity of a ToF-CIMS towards a wide suite of routinely detected multifunctional organic molecules for which no calibration standards exist. We describe the scanning procedure and collision limit determination, and we show results from the application of these constraints to the measurement of organic aerosol composition at two different field locations.

  15. Mechanism of chlorinating lanthanum oxide and cerium oxide with ammonium chloride

    Institute of Scientific and Technical Information of China (English)

    朱国才; 李赋屏; 肖明贵

    2003-01-01

    Using ammonium chloride(NH4Cl)as a chlorinating agent,the effects of chlorinating temperature,at 300℃ for 90 min,and have no advantage to chlorination of lanthanum and cerium oxides at higher temperature.The thermal decomposition of LaCl3 and CeCl3 is carried out to explore the mechanism of chlorinating lanthanum and cerium oxides.At the same time,the chlorination of lanthanum and cerium oxides is not devoted to the HCl decomposed from NH4Cl,but to NH4Cl directly taking part in the chlorination of La2O3 and CeO2.The lanthanum and cerium oxides in chlorination firstly form intermediate LaOCl and CeOCl,and then transfer to LaCl3 and CeCl3,fither prove the existence of the intermediates LaOCl and CeOCl.Therefore the chlorinating temperature and time should strictly be controlled when the lanthanum oxide and cerium oxide are chlorinated with NH4 Cl.And over-dosage of NH4 Cl should be also applied in the process of chlorination.

  16. First Derivative UV Spectra of Surface Water as a Monitor of Chlorination in Drinking Water Treatment

    Directory of Open Access Journals (Sweden)

    V. Zitko

    2001-01-01

    Full Text Available Many countries require the presence of free chlorine at about 0.1 mg/l in their drinking water supplies. For various reasons, such as cast-iron pipes or long residence times in the distribution system, free chlorine may decrease below detection limits. In such cases it is important to know whether or not the water was chlorinated or if nonchlorinated water entered the system by accident. Changes in UV spectra of natural organic matter in lakewater were used to assess qualitatively the degree of chlorination in the treatment to produce drinking water. The changes were more obvious in the first derivative spectra. In lakewater, the derivative spectra have a maximum at about 280 nm. This maximum shifts to longer wavelengths by up to 10 nm, decreases, and eventually disappears with an increasing dose of chlorine. The water treatment system was monitored by this technique for over 1 year and changes in the UV spectra of water samples were compared with experimental samples treated with known amounts of chlorine. The changes of the UV spectra with the concentration of added chlorine are presented. On several occasions, water, which received very little or no chlorination, may have entered the drinking water system. The results show that first derivative spectra are potentially a tool to determine, in the absence of residual chlorine, whether or not surface water was chlorinated during the treatment to produce potable water.

  17. Formation of disinfection by-products in the ultraviolet/chlorine advanced oxidation process.

    Science.gov (United States)

    Wang, Ding; Bolton, James R; Andrews, Susan A; Hofmann, Ron

    2015-06-15

    Disinfection by-product (DBP) formation may be a concern when applying ultraviolet light and free chlorine (UV/chlorine) as an advanced oxidation process (AOP) for drinking water treatment, due to typically large chlorine doses (e.g. 5-10 mg L(-1) as free chlorine). A potential mitigating factor is the low chlorine contact times for this AOP treatment (e.g. seconds). Full-scale and pilot-scale test results showed minimal trihalomethane (THM) and haloacetic acid (HAA) formation during UV/chlorine treatment, while dichloroacetonitrile (DCAN) and bromochloroacetonitrile (BCAN) were produced rapidly. Adsorbable organic halide (AOX) formation was significant when applying the UV/chlorine process in water that had not been previously chlorinated, while little additional formation was observed in prechlorinated water. Chlorine photolysis led to chlorate and bromate formation, equivalent to approximately 2-17% and 0.01-0.05% of the photolyzed chlorine, respectively. No perchlorate or chlorite formation was observed. During simulated secondary disinfection of AOP-treated water, DBP formation potential for THMs, HAAs, HANs, and AOX was observed to increase approximately to the same extent as was observed for pretreatment using the more common AOP of UV combined with hydrogen peroxide (UV/H2O2).

  18. Effects of combined UV and chlorine treatment on chloroform formation from triclosan.

    Science.gov (United States)

    Ben, Weiwei; Sun, Peizhe; Huang, Ching-Hua

    2016-05-01

    The co-exposure to UV irradiation and free chlorine may occur in certain drinking water and wastewater treatment systems. This study investigated the effects of simultaneous low pressure ultraviolet (LPUV) irradiation and free chlorination on the formation of chloroform from triclosan which is a commonly used antibacterial agent. Different treatment systems (i.e., combined UV/chlorine, UV alone, and chlorine alone) were applied to examine the degradation of triclosan and formation of chloroform. The fate of representative intermediates, including chlorinated triclosan, dechlorinated triclosan intermediates and 2,4-dichlorophenol, were tracked to deduce the effect of combined UV/chlorine on the transformation of chloroform formation precursors. The relation between intermediates degradation and chloroform formation was investigated in depth by conducting stepwise experiments with UV and chlorine in different sequences. Results indicate that the combined UV/chlorine notably enhanced the chloroform formation from triclosan. From the reaction mechanism perspective the combined UV/chlorine, where the direct photolysis may play an important role, could accelerate the decay of intermediates and facilitate the generation of productive chloroform precursors. The radicals had modest influence on the degradation of triclosan and intermediates and partly hindered the formation of chloroform. These results emphasize the necessity of considering disinfection by-products formation in the application of combined UV/chlorine technology during water treatment.

  19. CHEMICAL ANALYSIS OF REVERSE OSMOSIS MEMBRANE AND XAD RESIN ADSORPTION CONCENTRATES OF WATER DISINFECTED BY CHLORINATION OR OZONATION/CHLORINATION PROCESSES

    Science.gov (United States)

    Chemical Analysis of Reverse Osmosis Membrane and XAD Resin Adsorption Concentrates of Water Disinfected by Chlorination or Ozonation/Chlorination Processes.J. E. Simmons1, S.D. Richardson2, K.M. Schenck3, T. F. Speth3, R. J. Miltner3 and A. D. Thruston21 NHEE...

  20. Chlorine Nuclear Quadrupole Hyperfine Structure in the Vinyl - Chloride Complex

    Science.gov (United States)

    Leung, Helen O.; Marshall, Mark D.; Messinger, Joseph P.

    2015-06-01

    The microwave spectrum of the vinyl chloride--hydrogen chloride complex, presented at last year's symposium, is greatly complicated by the presence of two chlorine nuclei as well as an observed, but not fully explained tunneling motion. Indeed, although it was possible at that time to demonstrate conclusively that the complex is nonplanar, the chlorine nuclear quadrupole hyperfine splitting in the rotational spectrum resisted analysis. With higher resolution, Balle-Flygare Fourier transform microwave spectra, the hyperfine structure has been more fully resolved, but appears to be perturbed for some rotational transitions. It appears that knowledge of the quadrupole coupling constants will provide essential information regarding the structure of the complex, specifically the location of the hydrogen atom in HCl. Our progress towards obtaining values for these constants will be presented.

  1. Challenges in subsurface in situ remediation of chlorinated solvents

    DEFF Research Database (Denmark)

    Broholm, Mette Martina; Fjordbøge, Annika Sidelmann; Christiansen, Camilla Maymann

    2014-01-01

    Chlorinated solvent source zones in the subsurface pose a continuous threat to groundwater quality at many sites worldwide. In situ remediation of these sites is particularly challenging in heterogeneous fractured media and where the solvents are present as DNAPL. In situ remediation by chemical...... as well as biological degradation of chlorinated solvents is a contact sport and requires direct contact between the contaminant and the reactants and/or degrading microorganisms. In fractured geologic media, where contaminants have spread to the low permeability matrix by diffusion, the contact between......-clay mixing for contact; hydrophobic and/or mobile nano-reactants targeting DNAPL. The complexity of the technologies varies greatly and the current level of implementation ranges from multiple full scale applications to bench scale testing. However, the basic degradation reaction involved is usually well...

  2. Chemisorption of chlorine and sulfur dioxide on zinc oxide

    Energy Technology Data Exchange (ETDEWEB)

    Vinokurov, A.A.; Derlyukova, L.E.; Evdokimov, V.I.

    1987-03-10

    The chemisorption of sulfur dioxide and chlorine on the surface of zinc oxide and the change in the electric conductivity of ZnO during the chemisorption process were studied. It was shown that both gases induce a negative charging of the surface of zinc oxide. The kinetics of the chemisorption of Cl/sub 2/ and SO/sub 2/ is described by the Zel'dovich-Roginskii equation. The mutual influence of sulfur dioxide and chlorine during successive chemisorption was investigated. It was shown that the nature of the mutual influence depends on the temperature and the sequence of action of the gases. The results obtained were analyzed from the standpoint of the electronic theory of chemisorption on semiconductors.

  3. Pressured liquid chlorine leakage accident simulation in highway tunnel

    Directory of Open Access Journals (Sweden)

    LI Jianfeng, LIU Mao, WANG Wei

    2010-03-01

    Full Text Available With the national economic development, China's transportation infrastructure has also made great progress, particularly in the highway. How to reduce the accident consequence that occurred in the highway tunnel has been the tropical topic in China. The liquid Chlorine accidental leakage in highway tunnel was exemplified for the poisonous gas dispersion consequence analysis using computational fluid dynamics. First, the GAMBIT code was used to create geometrical models and generate meshes. Second, by using the FLUENT code, the Chlorine gas dispersion in the highway tunnel was simulated and the scenarios with different leak sources were discussed. Case study shows that the FLUENT code was useful on the simulation of gas dispersion in highway tunnel that serves the prerequisite for the further research.

  4. MECHANISM OF CHLORATE FORMATION IN CHLORINE DIOIXDE DELIGNIFICATION

    Institute of Scientific and Technical Information of China (English)

    Byung-HoYoon; Li-JunWangI; Se-JongKim

    2004-01-01

    The effect of pH on chlorate formation duringchlorine dioxide delignification of oxygen delignifiedkraft pulp was studied. Chlorate formation was foundto increase slightly when pH was increased from 1.8to 2.5, further increase of pH decreased chlorateformation.The above phenomenon is explained by thecombination of two mechanisms, one by the reactionbetween hypochlorous acid and chlorite, another bythe effect of chlorine on the regeneration of chlorinedioxide. The first mechanism suggests that chlorateformation is highly dependent on HC10concentration which decreases with increasing pHand causes chlorate formation to behave in the sametrend. The second mechanism suggests that chlorinefavors the regeneration of chlorine dioxide whileHCIO favors chlorate formation, thus lowering thepH from about 4 to the acidic end should decreaseschlorate formation. Thethe maximum formation2.5.two opposite effects lead toof chlorate at around pH

  5. Chlorine trifluoride (1963); Le trifluorure de chlore (1963)

    Energy Technology Data Exchange (ETDEWEB)

    Vincent, L.M.; Gillardeau, J. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1963-07-01

    This monograph on chlorine trifluoride may be considered as a working tool useful in gaseous diffusion research. It consists of data gathered from the literature and includes furthermore a certain amount of original data. This monograph groups together the physical, chemical and physiological properties of chlorine trifluoride, as well as the preparation and analytical methods. It has been thought wise to add some technological information, and the safety regulations governing its use. (authors) [French] Cette monographie sur le trifluorure de chlore doit etre consideree comme un instrument de travail dans le cadre des recherches sur la diffusion gazeuse. Il etait necessaire de grouper les donnees eparses dans la litterature. Elle comprend en outre un certain nombre de donnees originales. Cette monographie groupe les proprietes physiques, chimiques et physiologiques du trifluorure de chlore, ainsi que ses methodes de preparation et d'analyse. On a juge utile de joindre des indications technologiques et les consignes de securite concernant son emploi. (auteurs)

  6. Chlorinated alkaloids in Menispermum dauricum DC: root culture.

    Science.gov (United States)

    Sugimoto, Y; Babiker, H A; Saisho, T; Furumoto, T; Inanaga, S; Kato, M

    2001-05-18

    Feeding experiments using (36)Cl showed that Menispermum dauricum root culture produces four alkaloids containing chlorine. They included the novel alkaloids dauricumine and dauricumidine as well as the known alkaloids acutumine and acutumidine. The structures of novel alkaloids were established by spectroscopic, crystallographic, and chemical methods. These four alkaloids were labeled with (36)Cl, isolated, and fed independently to root cultures. Mutual conversion between acutumine and acutumidine, and between dauricumine and dauricumidine by N-methylation and N-demethylation, was demonstrated. Moreover, dauricumine was converted to acutumine and acutumidine. Epimerization of acutumidine to dauricumidine or vice versa was not observed. These results suggest that dauricumine is the first chlorinated alkaloid formed in cultured M. dauricum roots. Skewed distribution of radioactivity derived from labeled dauricumine is proof that epimerization at C-1 proceeds at a lower rate than N-demethylation.

  7. Phytoscreening of BTEX and chlorinated solvents by tree coring

    DEFF Research Database (Denmark)

    Nielsen, Mette Algreen; Broholm, Mette Martina; Trapp, Stefan

    Background/Objectives. Site characterization is often time consuming and a financial burden for the site owners, which raises a demand for rapid and inexpensive screening methods. Tree coring is a phytoscreening method useful for detection of contamination with organic compounds. The method takes......(s). The measured concentrations are also compared to concentrations detected in soil and/or groundwater. Furthermore, the two screening technologies Tree coring and Soil air sampling have been compared to evaluate the feasibility of the tree coring method. Results/Lessons Learned. The method of tree coring can...... detect contamination with BTEX and chlorinated solvents in the shallow subsurface. The uptake of BTEX into trees varies to a greater extent with the site conditions and tree species than chlorinated solvents, which lead to greater uncertainty. Tree coring is semi-quantitative, low...

  8. Antibacterial effect of chlorine dioxide and hyaluronate on dental biofilm

    OpenAIRE

    Al-bayaty, F.; Taiyeb-ali, T.; Abdulla, M. A.; Hashim, F.

    2010-01-01

    The objective of this study is to investigate antimicrobial action of chlorine dioxide (ClO(2)) gel and hyaluronate gel (Gengigel (R)) on dental biofilm. Pooled supra and subgingival dental biofilm were obtained from healthy individuals and incubated aerobically and anaerobically. Plaque bacteria investigated including Streptococcus constellatus, Streptococcus mitis, Eikenella corrodens, Fusobacterium nucleatum, dental plaque pool samples (aerobic and anaerobic) and Staphylococcus aureus and ...

  9. Evaluation of low-chlorine TATB from a production source

    Energy Technology Data Exchange (ETDEWEB)

    Stallings, T.L.; Osborn, A.G.; Johnson, H.D.; Duncan, A.A.; Schaffer, C.L.

    1981-08-01

    Six production lots of low-chlorine TATB powder have been evaluated. Five of the lots were made by a wet-amination process and the other was made by an emulsion-amination process. LX-17 physical properties specimens made from the five wet-aminated TATB lots were exceptionally strong and comparable to dry-aminated TATB, while the emulsion-aminated lot of TATB had lower strength.

  10. SEPARATION OF NEPTUNIUM FROM PLUTONIUM BY CHLORINATION AND SUBLIMATION

    Science.gov (United States)

    Fried, S.M.

    1958-11-18

    A process is described for separating neptunium from plutonium. The method consists in chlorinating a mixture of the oxides of Np and Pu by contacting the mixture with carbon tetrachloride at about 500 icient laborato C. ln this manner the Np is converted to the tetrachlorlde and the Pu converted to the trichloride. Since NpCl/sub 4/ is more latile than PuCl/sub 3/, the separation ls effected by vaporing sad subsequently condenslng the NpCl/sub 4/.

  11. Biological instability in a chlorinated drinking water distribution network.

    Science.gov (United States)

    Nescerecka, Alina; Rubulis, Janis; Vital, Marius; Juhna, Talis; Hammes, Frederik

    2014-01-01

    The purpose of a drinking water distribution system is to deliver drinking water to the consumer, preferably with the same quality as when it left the treatment plant. In this context, the maintenance of good microbiological quality is often referred to as biological stability, and the addition of sufficient chlorine residuals is regarded as one way to achieve this. The full-scale drinking water distribution system of Riga (Latvia) was investigated with respect to biological stability in chlorinated drinking water. Flow cytometric (FCM) intact cell concentrations, intracellular adenosine tri-phosphate (ATP), heterotrophic plate counts and residual chlorine measurements were performed to evaluate the drinking water quality and stability at 49 sampling points throughout the distribution network. Cell viability methods were compared and the importance of extracellular ATP measurements was examined as well. FCM intact cell concentrations varied from 5×10(3) cells mL(-1) to 4.66×10(5) cells mL(-1) in the network. While this parameter did not exceed 2.1×10(4) cells mL(-1) in the effluent from any water treatment plant, 50% of all the network samples contained more than 1.06×10(5) cells mL(-1). This indisputably demonstrates biological instability in this particular drinking water distribution system, which was ascribed to a loss of disinfectant residuals and concomitant bacterial growth. The study highlights the potential of using cultivation-independent methods for the assessment of chlorinated water samples. In addition, it underlines the complexity of full-scale drinking water distribution systems, and the resulting challenges to establish the causes of biological instability.

  12. Biological instability in a chlorinated drinking water distribution network.

    Directory of Open Access Journals (Sweden)

    Alina Nescerecka

    Full Text Available The purpose of a drinking water distribution system is to deliver drinking water to the consumer, preferably with the same quality as when it left the treatment plant. In this context, the maintenance of good microbiological quality is often referred to as biological stability, and the addition of sufficient chlorine residuals is regarded as one way to achieve this. The full-scale drinking water distribution system of Riga (Latvia was investigated with respect to biological stability in chlorinated drinking water. Flow cytometric (FCM intact cell concentrations, intracellular adenosine tri-phosphate (ATP, heterotrophic plate counts and residual chlorine measurements were performed to evaluate the drinking water quality and stability at 49 sampling points throughout the distribution network. Cell viability methods were compared and the importance of extracellular ATP measurements was examined as well. FCM intact cell concentrations varied from 5×10(3 cells mL(-1 to 4.66×10(5 cells mL(-1 in the network. While this parameter did not exceed 2.1×10(4 cells mL(-1 in the effluent from any water treatment plant, 50% of all the network samples contained more than 1.06×10(5 cells mL(-1. This indisputably demonstrates biological instability in this particular drinking water distribution system, which was ascribed to a loss of disinfectant residuals and concomitant bacterial growth. The study highlights the potential of using cultivation-independent methods for the assessment of chlorinated water samples. In addition, it underlines the complexity of full-scale drinking water distribution systems, and the resulting challenges to establish the causes of biological instability.

  13. Chlorine dioxide against bacteria and yeasts from the alcoholic fermentation

    Science.gov (United States)

    Meneghin, Silvana Perissatto; Reis, Fabricia Cristina; de Almeida, Paulo Garcia; Ceccato-Antonini, Sandra Regina

    2008-01-01

    The ethanol production in Brazil is carried out by fed-batch or continuous process with cell recycle, in such way that bacterial contaminants are also recycled and may be troublesome due to the substrate competition. Addition of sulphuric acid when inoculum cells are washed can control the bacterial growth or alternatively biocides are used. This work aimed to verify the effect of chlorine dioxide, a well-known biocide for bacterial decontamination of water and equipments, against contaminant bacteria (Bacillus subtilis, Lactobacillus plantarum, Lactobacillus fermentum and Leuconostoc mesenteroides) from alcoholic fermentation, through the method of minimum inhibitory concentration (MIC), as well as its effect on the industrial yeast inoculum. Lower MIC was found for B. subtilis (10 ppm) and Leuconostoc mesenteroides (50 ppm) than for Lactobacillus fermentum (75 ppm) and Lactobacillus plantarum (125 ppm). Additionally, these concentrations of chlorine dioxide had similar effects on bacteria as 3 ppm of Kamoran® (recommended dosage for fermentation tanks), exception for B. subtilis, which could not be controlled at this Kamoran® dosage. The growth of industrial yeasts was affected when the concentration of chlorine dioxide was higher than 50 ppm, but the effect was slightly dependent on the type of yeast strain. Smooth yeast colonies (dispersed cells) seemed to be more sensitive than wrinkled yeast colonies (clustered cells/pseudohyphal growth), both isolated from an alcohol-producing unit during the 2006/2007 sugar cane harvest. The main advantage in the usage of chlorine dioxide that it can replace antibiotics, avoiding the selection of resistant populations of microorganisms. PMID:24031227

  14. Natural chlorine and fluorine in the atmosphere, water and precipitation

    Science.gov (United States)

    Friend, James P.

    1990-01-01

    The geochemical cycles of chlorine and fluorine are surveyed and summarized as framework for the understanding of the global natural abundances of these species in the atmosphere, water, and precipitation. In the cycles the fluxes into and out of the atmosphere can be balanced within the limits of our knowledge of the natural sources and sinks. Sea salt from the ocean surfaces represent the predominant portion of the source of chlorine. It is also an important source of atmospheric fluorine, but volcanoes are likely to be more important fluorine sources. Dry deposition of sea salt returns about 85 percent of the salt released there. Precipitation removes the remainder. Most of the sea salt materials are considered to be cyclic, moving through sea spray over the oceans and either directly back to the oceans or deposited dry and in precipitation on land, whence it runs off into rivers and streams and returns to the oceans. Most of the natural chlorine in the atmosphere is in the form of particulate chloride ion with lesser amounts as gaseous inorganic chloride and methyl chloride vapor. Fluorine is emitted from volcanoes primarily as HF. It is possible that HF may be released directly form the ocean surface but this has not been confirmed by observation. HCl and most likely HF gases are released into the atmosphere by sea salt aerosols. The mechanism for the release is likely to be the provision of protons from the so-called excess sulfate and HNO3. Sea salt aerosol contains fluorine as F(-), MgF(+), CaF(+), and NaF. The concentrations of the various species of chlorine and fluorine that characterize primarily natural, unpolluted atmospheres are summarized in tables and are discussed in relation to their fluxes through the geochemical cycle.

  15. The pool chlorine hypothesis and asthma among boys.

    LENUS (Irish Health Repository)

    Cotter, A

    2012-01-31

    Swimming pool sanitation has largely been concerned with the microbiological quality of pool water, which is normally treated using a number of chlorine products. Recent studies have pointed to the potential hazards of chlorine by-products to the respiratory epithelium, particularly in indoor, poorly ventilated, pools. The aim of our study was to elucidate whether chronic exposure to indoor chlorinated swimming pools was associated with an increased likelihood of the development of asthma in boys. METHODS: The subjects were boys aged between 6 and 12 years. Data was collected by means of parental responses to a standardized asthma questionnaire (ISAAC: International Study of Asthma and Allergies in Childhood), supplemented with additional questions regarding frequency of attendance, number of years attendance, whether the child is a swimming team member. The questionnaire return rate was 71\\/% (n = 121). 23 boys were excluded on the basis that they had asthma before they started swimming (n = 97). There was a significant association between number of years a boy had been swimming and the likelihood of wheezing in the last 12 months (p = 0.009; OR = 1.351; 95% CI = 1.077-1.693) and diagnosed asthma (p = 0.046; OR = 1.299; 95% CI = 1.004-1.506). The greater the number the number of years a boy had been attending an indoor, chlorinated pool, the greater the likelihood of wheezing in the last 12 months or "had asthma". Age, parental smoking habits and being a swimming team member had no association with any of the asthma variables examined. Swimming pool attendance may be a risk factor in asthma in boys.

  16. The influence of chlorine on the gasification of wood

    Energy Technology Data Exchange (ETDEWEB)

    Scala, C. von; Struis, R.; Stucki, S. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1997-06-01

    Chlorides of the heavy metals copper, lead and zinc inhibit the CO{sub 2}-gasification reaction of charcoal. This is observed either by impregnation the wood with the salts before pyrolysis or by mechanically mixing the salts with the charcoal before gasification. Charcoal impregnated or mixed with ammonium chloride reacts more slowly than untreated charcoal. Treating the charcoal with HCl also influences negatively the gasification reactivity, indicating that chlorine plays an important role in the gasification. (author) 2 figs., 4 refs.

  17. Mass transfer properties of chlorinated aromatic polyamide reverse osmosis membranes

    OpenAIRE

    Ettori, Axel; Gaudichet-Maurin, Emmanuelle; Aimar, Pierre; Causserand, Christel

    2012-01-01

    International audience; Water (A) and solute (B) permeability of aromatic polyamide (PA) reverse osmosis membranes (RO) were monitored under varying applied pressure, solute nature and concentration to assess their evolution after exposure of the membrane to free chlorine. Above a threshold value of 400 ppm h HOCl water permeability was influenced by permeation conditions during both filtration of ultrapure water (UP water) and reverse osmosis of salts performed sequentially. Water permeabili...

  18. Chlorine Analysis by Diode Laser Atomic Absorption Spectrometry

    Institute of Scientific and Technical Information of China (English)

    Joachim Koch; Aleksandr Zybin; Kay Niemax

    2000-01-01

    The general characteristics of Diode Laser Absorption Spectrometry (DLAAS) in low pressure plasmas particulary with respect to the detection of non-metals are comprehensively recapitulated and discussed. Furthermore, a detector, which is based on DLAAS in a microwave-induced low pressure plasma as an alternative technique for halogene-specific analysis of volatile compounds and polymeric matrices is described. The analytical capability of the technique is demonstrated on the chlorine-specific analysis of ablated polymer fragments as well as gas chromatographically separated hydrocarbons. Since the measurements were carried out by means of a balanced-heterodyne detection scheme, different technical noise contributions, such as laser excess and RAM noise could efficiently be suppressed and the registered absorption was limited only by the principal shot noise. Thus, in the case of the polymer analysis a chlorine-specific absolute detection limit of 10 pg could be achieved. Furthermore, fundamental investigations concerning the influence of hydrocarbons on the dissociation capability of the microwave induced plasma were performed. For this purpose, the carbon-, chlorine-and hydrogen-specific stoichiometry of the compounds were empirically determined. Deviations from the exspected proportions were found to be insignificant, implying the possibility of internal standardization relative to the response of a reference sample.

  19. Behavior and control of chlorine in dyestuff residue incineration

    Institute of Scientific and Technical Information of China (English)

    YAN Jian-hua; TAN Zhong-xin; JIANG Xue-guang; CHI Yong; CEN Ke-fa

    2006-01-01

    Dyestuff residue, a type of hazardous waste, is incinerated in the tubular furnace, and thermodynamic equilibrium model is used to calculate and analyze the chlorine behavior. The HCl emission and its effects on the behaviors of heavy metals are studied.Meanwhile, the effects of three dechlorine reagents are predicted at a high temperature. Results show that HCl emission is dependent on incineration temperature. The HCl evaporated mainly derives from the organic chlorine. Under the working condition of 500--900℃, the main products of Hg, Pb, Cu, Ni, Zn, and Mn in reaction with HCl are HgCl2 (g), PbCl4(g), PbCl2 (g), (CuCl)3 (g), NiCl2 (s),NiCl2 (g), ZnCl2 (s), ZnCl2 (g), Zn (g), MnCl2 (s), and MnCl2 (g), respectively. Among the three dechlorine reagents, CaCO3 is optimal to remove chlorine at high temperature, little of HCl is released below 800℃, whereas Fe3O4 is unstable at high temperature.

  20. Depletion of chlorine into HCl ice in a protostellar core

    CERN Document Server

    Kama, M; Lopez-Sepulcre, A; Wakelam, V; Dominik, C; Ceccarelli, C; Lanza, M; Lique, F; Ochsendorf, B B; Lis, D C; Caballero, R N; Tielens, A G G M

    2014-01-01

    The freezeout of gas-phase species onto cold dust grains can drastically alter the chemistry and the heating-cooling balance of protostellar material. In contrast to well-known species such as carbon monoxide (CO), the freezeout of various carriers of elements with abundances $<10^{-5}$ has not yet been well studied. Our aim here is to study the depletion of chlorine in the protostellar core, OMC-2 FIR 4. We observed transitions of HCl and H2Cl+ towards OMC-2 FIR 4 using the Herschel Space Observatory and Caltech Submillimeter Observatory facilities. Our analysis makes use of state of the art chlorine gas-grain chemical models and newly calculated HCl-H$_{2}$ hyperfine collisional excitation rate coefficients. A narrow emission component in the HCl lines traces the extended envelope, and a broad one traces a more compact central region. The gas-phase HCl abundance in FIR 4 is 9e-11, a factor of only 0.001 that of volatile elemental chlorine. The H2Cl+ lines are detected in absorption and trace a tenuous fo...