Iodide-Photocatalyzed Reduction of Carbon Dioxide to Formic Acid with Thiols and Hydrogen Sulfide.

Science.gov (United States)

Berton, Mateo; Mello, Rossella; González-Núñez, María Elena

2016-12-20

The photolysis of iodide anions promotes the reaction of carbon dioxide with hydrogen sulfide or thiols to quantitatively yield formic acid and sulfur or disulfides. The reaction proceeds in acetonitrile and aqueous solutions, at atmospheric pressure and room temperature by irradiation using a low-pressure mercury lamp. This transition-metal-free photocatalytic process for CO 2 capture coupled with H 2 S removal may have been relevant as a prebiotic carbon dioxide fixation. © 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Potassium iodide potentiates antimicrobial photodynamic inactivation mediated by Rose Bengal: in vitro and in vivo studies

Science.gov (United States)

Wen, Xiang; Zhang, Xiaoshen; Szewczyk, Grzegorz; ElHussien, Ahmed; Huang, Ying-Ying; Sarna, Tadeusz; Hamblin, Michael R.

2018-02-01

Rose Bengal (RB) is a halogenated xanthene dye that has been used to mediate antimicrobial photodynamic inactivation. While highly active against Gram-positive bacteria, RB is largely inactive in killing Gram-negative bacteria. We have discovered that addition of the non-toxic salt potassium iodide (100mM) potentiates green light (540nm)-mediated killing by up to six extra logs with Gramnegative bacteria Escherichia coli and Pseudomonas aeruginosa,Gram-positive methicillin resistant Staphylococcus aureus, and fungal yeast Candida albicans. The mechanism is proposed to be singlet oxygen addition to iodide anion to form peroxyiodide, which decomposes into radicals, finally forms hydrogen peroxide and molecular iodine. The effects of these different bactericidal species can be teased apart by comparing killing in three different scenarios: (1) cells+RB+KI are mixed together then illuminated with green light; (2) cells+RB are centrifuged then KI added then green light; (3) RB+KI+green light then cells added after light. We showed that KI could potentiate RBPDT in a mouse model of skin abrasions infected with bioluminescent P.aeruginosa.

Methyl Iodide Decomposition at BWR Conditions

International Nuclear Information System (INIS)

Pop, Mike; Bell, Merl

2012-09-01

Based on favourable results from short-term testing of methanol addition to an operating BWR plant, AREVA has performed numerous studies in support of necessary Engineering and Plant Safety Evaluations prior to extended injection of methanol. The current paper presents data from a study intended to provide further understanding of the decomposition of methyl iodide as it affects the assessment of methyl iodide formation with the application of methanol at BWR Plants. This paper describes the results of the decomposition testing under UV-C light at laboratory conditions and its effect on the subject methyl iodide production evaluation. The study as to the formation and decomposition of methyl iodide as it is effected by methanol addition is one phase of a larger AREVA effort to provide a generic plant Safety Evaluation prior to long-term methanol injection to an operating BWR. Other testing phases have investigated the compatibility of methanol with fuel construction materials, plant structural materials, plant consumable materials (i.e. elastomers and coatings), and ion exchange resins. Methyl iodide is known to be very unstable, typically preserved with copper metal or other stabilizing materials when produced and stored. It is even more unstable when exposed to light, heat, radiation, and water. Additionally, it is known that methyl iodide will decompose radiolytically, and that this effect may be simulated using ultra-violet radiation (UV-C) [2]. In the tests described in this paper, the use of a UV-C light source provides activation energy for the formation of methyl iodide. Thus is similar to the effect expected from Cherenkov radiation present in a reactor core after shutdown. Based on the testing described in this paper, it is concluded that injection of methanol at concentrations below 2.5 ppm in BWR applications to mitigate IGSCC of internals is inconsequential to the accident conditions postulated in the FSAR as they are related to methyl iodide formation

Decomposing method for ion exchange resin

International Nuclear Information System (INIS)

Sako, Takeshi; Sato, Shinshi; Akai, Yoshie; Moniwa, Shinobu; Yamada, Kazuo

1998-01-01

The present invention concerns a method of decomposing ion exchange resins generated in a nuclear power plant to carbon dioxide reliably in a short period of time. (1) The ion exchange resins are mixed with water, and then they are kept for a predetermined period of time in the presence of an inert gas at high temperature and high pressure exceeding the critical point of water to decompose the ion exchange resins. (2) The ion exchange resins is mixed with water, an oxidant is added and they are kept for a predetermined time in the presence of an inert gas at a high temperature and a high pressure exceeding a critical point of water of an inert gas at a high temperature to decompose the ion exchange resins. (3) An alkali or acid is added to ion exchange resins and water to control the hydrogen ion concentration in the solution and the ion exchange resins are decomposed in above-mentioned (1) or (2). Sodium hydroxide is used as the alkali and hydrochloric acid is used as the acid. In addition, oxygen, hydrogen peroxide or ozone is used as an oxidant. (I.S.)

Method of decomposing radioactive organic solvent wastes

International Nuclear Information System (INIS)

Uki, Kazuo; Ichihashi, Toshio; Hasegawa, Akira; Sato, Tatsuaki

1986-01-01

Purpose: To decompose radioactive organic solvent wastes or radioactive hydrocarbon solvents separated therefrom into organic materials under moderate conditions, as well as greatly decrease the amount of secondary wastes generated. Method: Radioactive organic solvent wastes comprising an organic phosphoric acid ester ingredient and a hydrocarbon ingredient as a diluent therefor, or radioactive hydrocarbon solvents separated therefrom are oxidatively decomposed by hydrogen peroxide in an aqueous phosphoric acid solution of phosphoric acid metal salts finally into organic materials to perform decomposing treatment for the radioactive organic solvent wastes. The decomposing reaction is carried out under relatively moderate conditions and cause less burden to facilities or the likes. Further, since the decomposed liquid after the treatment can be reused for the decomposing reaction as a catalyst solution secondary wastes can significantly be decreased. (Yoshihara, H.)

Radiolytic formation of organic iodides from organic compounds released from ripolin paint

International Nuclear Information System (INIS)

Attia, S.; Evans, G.J.

2002-01-01

The impact of a serious nuclear reactor accident is governed to a large extent by the possible release of airborne organic iodides to the environment. This research examines the identification and behavior of organic iodides formed in the containment due to the release of organic compounds from Ripolin paint, into the aqueous phase, following a nuclear reactor accident. A bench scale apparatus installed in the irradiation chamber of a Gammacell was used to analyze the formation of organic iodides. Iodo-organics, transferred to the gas phase above irradiated aqueous samples, were analyzed using a Thermal Desorption method coupled with gas chromatography and mass spectrometry. Detailed studies of the identity of the organic compounds released and the organic iodides formed were conducted. The effects of parameters such as irradiation dose were also examined. All the organic iodides formed, under radiolytic conditions, were identified as iodo-alkanes. The organic compounds that were released from the Ripolin paint, such as methyl isobutyl ketone, were found to decompose, by a series of reactions, to produce the organic iodides. The precursor organic compounds and the organic iodides formed were observed to consist of the same alkyl group. These results indicate that organic compounds released from surface paints directly influence the formation of radiolytic organic iodide. (author)

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.

A novel sodium iodide and ammonium molybdate co-catalytic system for the efficient synthesis of 2-benzimidazoles using hydrogen peroxide under ultrasound irradiation.

Science.gov (United States)

Bai, Guo-Yi; Lan, Xing-Wang; Chen, Guo-Feng; Liu, Xiao-Fang; Li, Tian-Yu; Shi, Ling-Juan

2014-03-01

The reaction of aldehydes and o-phenylenediamine for the preparation of 2-benzimidazoles has been studied using hydrogen peroxide as an oxidant under ultrasound irradiation at room temperature in this paper. The combination of substoichiometric sodium iodide and ammonium molybdate as co-catalysts, together with using small amounts of hydrogen peroxide, makes this transformation very efficient and attractive under ultrasound. Thus, a mild, green and efficient method is established to carry out this reaction in high yield. Copyright © 2013 Elsevier B.V. All rights reserved.

Study on gold concentrate leaching by iodine-iodide

Science.gov (United States)

Wang, Hai-xia; Sun, Chun-bao; Li, Shao-ying; Fu, Ping-feng; Song, Yu-guo; Li, Liang; Xie, Wen-qing

2013-04-01

Gold extraction by iodine-iodide solution is an effective and environment-friendly method. In this study, the method using iodine-iodide for gold leaching is proved feasible through thermodynamic calculation. At the same time, experiments on flotation gold concentrates were carried out and encouraging results were obtained. Through optimizing the technological conditions, the attained high gold leaching rate is more than 85%. The optimum process conditions at 25°C are shown as follows: the initial iodine concentration is 1.0%, the iodine-to-iodide mole ratio is 1:8, the solution pH value is 7, the liquid-to-solid mass ratio is 4:1, the leaching time is 4 h, the stirring intensity is 200 r/mim, and the hydrogen peroxide consumption is 1%.

Efficient photoreductive decomposition of N-nitrosodimethylamine by UV/iodide process

International Nuclear Information System (INIS)

Sun, Zhuyu; Zhang, Chaojie; Zhao, Xiaoyun; Chen, Jing; Zhou, Qi

2017-01-01

Highlights: • N-nitrosodimethylamine (NDMA) was effectively decomposed by UV/iodide process. • NDMA was completely converted to nontoxic end products by UV/iodide process. • The photoreductive process was mainly attributed to the attack of hydrated electrons on the photoexcited NDMA. • The elimination of toxic intermediates was greatly enhanced as pH increased, but its effect on NDMA removal was negligible. - Abstract: N-nitrosodimethylamine (NDMA) has aroused extensive concern as a disinfection byproduct due to its high toxicity and elevated concentration levels in water sources. This study investigates the photoreductive decomposition of NDMA by UV/iodide process. The results showed that this process is an effective strategy for the treatment of NDMA with 99.2% NDMA removed within 10 min. The depletion of NDMA by UV/iodide process obeyed pseudo-first-order kinetics with a rate constant (k_1) of 0.60 ± 0.03 min"−"1. Hydrated electrons (e_a_q"−) generated by the UV irradiation of iodide were proven to play a critical role. Dimethylamine (DMA) and nitrite (NO_2"−) were formed as the main intermediate products, which completely converted to formate (HCOO"−), ammonium (NH_4"+) and nitrogen (N_2). Therefore, not only the high efficiencies in NDMA destruction, but the elimination of toxic intermediates make UV/iodide process advantageous. A photoreduction mechanism was proposed: NDMA initially absorbed photons to a photoexcited state, and underwent a cleavage of N−NO bond under the attack of e_a_q"−. The solution pH had little impact on NDMA removal. However, alkaline conditions were more favorable for the elimination of DMA and NO_2"−, thus effectively reducing the secondary pollution.

Conceptual design of SO3 decomposer for thermo-chemical iodine-sulfur process pilot plant

International Nuclear Information System (INIS)

Akihiro Kanagawa; Seiji Kasahara; Atsuhiko Terada; Shinji Kubo; Ryutaro Hino; Yoshiyuki Kawahara; Masaharu Watabe; Hiroshi Fukui; Kazuo Ishino; Toshio Takahashi

2005-01-01

Thermo-chemical water-splitting cycle is a method to make an effective use of the high temperature nuclear heat for hydrogen production. Japan Atomic Energy Research Institute (JAERI) has been conducting R and D on HTGR and also on thermo-chemical hydrogen production by using a thermo-chemical iodine-sulfur cycle (IS process). Based on the test results and know-how obtained through a bench-scale tests of hydrogen production of about 30 NL/hr, JAERI has a plan to construct a pilot test plant heated by high temperature helium gas, which has a hydrogen production performance of 30 Nm 3 /hr and will be operated under the high pressure up to 2 MPa. One of the key components of the pilot test plant is a SO 3 decomposer under high temperature conditions up to 850 degree C and high pressure up to 2 MPa. In this paper, a concept of the SO 3 decomposer for the pilot test plant fabricated with SiC ceramics, a corrosion-resistant material is investigated. Preliminary analyses on temperature and flow-rate distributions in the SO 3 decomposer and on thermal stress were carried out. A SO 3 decomposer model was experimentally manufactured. (authors)

Efficient photoreductive decomposition of N-nitrosodimethylamine by UV/iodide process

Energy Technology Data Exchange (ETDEWEB)

Sun, Zhuyu; Zhang, Chaojie, E-mail: myrazh@tongji.edu.cn; Zhao, Xiaoyun; Chen, Jing; Zhou, Qi

2017-05-05

Highlights: • N-nitrosodimethylamine (NDMA) was effectively decomposed by UV/iodide process. • NDMA was completely converted to nontoxic end products by UV/iodide process. • The photoreductive process was mainly attributed to the attack of hydrated electrons on the photoexcited NDMA. • The elimination of toxic intermediates was greatly enhanced as pH increased, but its effect on NDMA removal was negligible. - Abstract: N-nitrosodimethylamine (NDMA) has aroused extensive concern as a disinfection byproduct due to its high toxicity and elevated concentration levels in water sources. This study investigates the photoreductive decomposition of NDMA by UV/iodide process. The results showed that this process is an effective strategy for the treatment of NDMA with 99.2% NDMA removed within 10 min. The depletion of NDMA by UV/iodide process obeyed pseudo-first-order kinetics with a rate constant (k{sub 1}) of 0.60 ± 0.03 min{sup −1}. Hydrated electrons (e{sub aq}{sup −}) generated by the UV irradiation of iodide were proven to play a critical role. Dimethylamine (DMA) and nitrite (NO{sub 2}{sup −}) were formed as the main intermediate products, which completely converted to formate (HCOO{sup −}), ammonium (NH{sub 4}{sup +}) and nitrogen (N{sub 2}). Therefore, not only the high efficiencies in NDMA destruction, but the elimination of toxic intermediates make UV/iodide process advantageous. A photoreduction mechanism was proposed: NDMA initially absorbed photons to a photoexcited state, and underwent a cleavage of N−NO bond under the attack of e{sub aq}{sup −}. The solution pH had little impact on NDMA removal. However, alkaline conditions were more favorable for the elimination of DMA and NO{sub 2}{sup −}, thus effectively reducing the secondary pollution.

Factors affecting the retention of methyl iodide by iodide-impregnated carbon

International Nuclear Information System (INIS)

Hyder, M.L.; Malstrom, R.A.

1991-01-01

This paper comprises two sets of studies of methyl iodide retention by iodide-impregnated carbon. In the first of these, the retention of the methyl iodide on the carbon surface and its subsequent evolution were observed directly by a technique of combustion and phosphorescence. In the second, the methyl iodide retention in a standard test was compared with surface area measurements and the concentration of unreacted iodine. A correlation among these parameters was identified and characterized. Carbon quality was varied through the selection of used material with differing service histories. Air from the Savannah River Site reactor buildings is vented through carbon beds for control of radioiodine before release to the atmosphere. The carbon used is North American Carbon Co. type GX-176 coconut shell carbon impregnated with 1% triethylenedimaine (TEDA) and 2% potassium iodide by weight. Replacement intervals for the carbon have been as long as thirty months. Analysis of samples withdrawn at much shorter times has shown that the TEDA is lost after a few months, and the performance of the carbon for methyl iodide retention is dependent on the iodide impregnant. Efficient methyl iodide retention is not a requirement for carbon in this service; however, methyl iodide retention as measured by the ASTM Test D3803 (method B) has been found to correlate well with other desirable properties of the carbon such as radiation stability. The studies undertaken here were intended to shed light on the changes taking place in this carbon during long-term service and to provide a basis for simpler measurements of carbon quality

Dynamic iodide trapping by tumor cells expressing the thyroidal sodium iodide symporter

International Nuclear Information System (INIS)

Dingli, David; Bergert, Elizabeth R.; Bajzer, Zeljko; O'Connor, Michael K.; Russell, Stephen J.; Morris, John C.

2004-01-01

The thyroidal sodium iodide symporter (NIS) in combination with various radioactive isotopes has shown promise as a therapeutic gene in various tumor models. Therapy depends on adequate retention of the isotope in the tumor. We hypothesized that in the absence of iodide organification, isotope trapping is a dynamic process either due to slow efflux or re-uptake of the isotope by cells expressing NIS. Iodide efflux is slower in ARH-77 and K-562 cells expressing NIS compared to a thyroid cell line. Isotope retention half times varied linearly with the number of cells expressing NIS. With sufficient NIS expression, iodide efflux is a zero-order process. Efflux kinetics in the presence or absence of perchlorate also supports the hypothesis that iodide re-uptake occurs and contributes to the retention of the isotope in tumor cells. Iodide organification was insignificant. In vivo studies in tumors composed of mixed cell populations confirmed these observations

Contrasting the surface ocean distribution of bromoform and methyl iodide; implications for boundary layer physics, chemistry and climate

Energy Technology Data Exchange (ETDEWEB)

Palmer, C J, E-mail: carl.j.palmer@gmail.co [Department of Oceanography, University of Cape Town, 7701 (South Africa)

2010-08-15

Bromoform and methyl iodide are both methane-like hydrocarbons with a halogen atom replacing one or more of the hydrogen atoms. Both of these compounds occur naturally in the environment as a result of their production from seaweed and kelp. They are of interest to climate science as a result of their catalytic destruction of boundary layer ozone (a potent greenhouse gas) and, specifically for methyl iodide, the proposed role in the formation of new cloud condensation nuclei with implications for climate. In this paper, the currently available data on the distribution of bromoform and methyl iodide are analysed and contrasted to show that the concentrations of bromoform and methyl iodide do not correlate, that, in contrast to bromoform, the parameterization of sea surface methyl iodide concentrations demands only the sea surface temperature, and that the pelagic distribution of methyl iodide appears to follow the solar zenith angle. These three observations together suggest that, while the pelagic source of bromoform is mostly biogenic, the source of methyl iodide is photochemical. This has implications for the understanding of planetary boundary layer chemistry and potential organohalogen mediated feedbacks to climate.

Contrasting the surface ocean distribution of bromoform and methyl iodide; implications for boundary layer physics, chemistry and climate

International Nuclear Information System (INIS)

Palmer, C J

2010-01-01

Bromoform and methyl iodide are both methane-like hydrocarbons with a halogen atom replacing one or more of the hydrogen atoms. Both of these compounds occur naturally in the environment as a result of their production from seaweed and kelp. They are of interest to climate science as a result of their catalytic destruction of boundary layer ozone (a potent greenhouse gas) and, specifically for methyl iodide, the proposed role in the formation of new cloud condensation nuclei with implications for climate. In this paper, the currently available data on the distribution of bromoform and methyl iodide are analysed and contrasted to show that the concentrations of bromoform and methyl iodide do not correlate, that, in contrast to bromoform, the parameterization of sea surface methyl iodide concentrations demands only the sea surface temperature, and that the pelagic distribution of methyl iodide appears to follow the solar zenith angle. These three observations together suggest that, while the pelagic source of bromoform is mostly biogenic, the source of methyl iodide is photochemical. This has implications for the understanding of planetary boundary layer chemistry and potential organohalogen mediated feedbacks to climate.

Electron stimulated reactions of methyl iodide coadsorbed with amorphous solid water

International Nuclear Information System (INIS)

Perry, C. C.; Faradzhev, N. S.; Madey, T. E.; Fairbrother, D. H.

2007-01-01

The electron stimulated reactions of methyl iodide (MeI) adsorbed on and suspended within amorphous solid water (ice) were studied using a combination of postirradiation temperature programmed desorption and reflection absorption infrared spectroscopy. For MeI adsorbed on top of amorphous solid water (ice), electron beam irradiation is responsible for both structural and chemical transformations within the overlayer. Electron stimulated reactions of MeI result principally in the formation of methyl radicals and solvated iodide anions. The cross section for electron stimulated decomposition of MeI is comparable to the gas phase value and is only weakly dependent upon the local environment. For both adsorbed MeI and suspended MeI, reactions of methyl radicals within MeI clusters lead to the formation of ethane, ethyl iodide, and diiodomethane. In contrast, reactions between the products of methyl iodide and water dissociation are responsible for the formation of methanol and carbon dioxide. Methane, formed as a result of reactions between methyl radicals and either parent MeI molecules or hydrogen atoms, is also observed. The product distribution is found to depend on the film's initial chemical composition as well as the electron fluence. Results from this study highlight the similarities in the carbon-containing products formed when monohalomethanes coadsorbed with amorphous solid water are irradiated by either electrons or photons

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.

Forensic entomology of decomposing humans and their decomposing pets.

Science.gov (United States)

Sanford, Michelle R

2015-02-01

Domestic pets are commonly found in the homes of decedents whose deaths are investigated by a medical examiner or coroner. When these pets become trapped with a decomposing decedent they may resort to feeding on the body or succumb to starvation and/or dehydration and begin to decompose as well. In this case report photographic documentation of cases involving pets and decedents were examined from 2009 through the beginning of 2014. This photo review indicated that in many cases the pets were cats and dogs that were trapped with the decedent, died and were discovered in a moderate (bloat to active decay) state of decomposition. In addition three cases involving decomposing humans and their decomposing pets are described as they were processed for time of insect colonization by forensic entomological approach. Differences in timing and species colonizing the human and animal bodies were noted as was the potential for the human or animal derived specimens to contaminate one another at the scene. Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

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. © 2015 Society for Endocrinology.

Hydrogen production by high-temperature gas-cooled reactor. Conceptual design of advanced process heat exchangers of the HTTR-IS hydrogen production system

International Nuclear Information System (INIS)

Sakaba, Nariaki; Ohashi, Hirofumi; Sato, Hiroyuki; Hara, Teruo; Kato, Ryoma; Kunitomi, Kazuhiko

2008-01-01

Nuclear hydrogen production is necessary in an anticipated hydrogen society that demands a massive quantity of hydrogen without economic disadvantage. Japan Atomic Energy Agency (JAEA) has launched the conceptual design study of a hydrogen production system with a near-term plan to connect it to Japan's first high-temperature gas-cooled reactor HTTR. The candidate hydrogen production system is based on the thermochemical water-splitting iodine sulphur (IS) process.The heat of 10 MWth at approximately 900degC, which can be provided by the secondary helium from the intermediate heat exchanger of the HTTR, is the energy input to the hydrogen production system. In this paper, we describe the recent progresses made in the conceptual design of advanced process heat exchangers of the HTTR-IS hydrogen production system. A new concept of sulphuric acid decomposer is proposed. This involves the integration of three separate functions of sulphuric acid decomposer, sulphur trioxide decomposer, and process heat exchanger. A new mixer-settler type of Bunsen reactor is also designed. This integrates three separate functions of Bunsen reactor, phase separator, and pump. The new concepts are expected to result in improved economics through construction and operation cost reductions because the number of process equipment and complicated connections between the equipment has been substantially reduced. (author)

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

2016-02-02

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.

Measurements of rates of some reactions related to radiolytic effect on aqueous iodide solution

International Nuclear Information System (INIS)

Shiraishi, H.; Okuda, H.; Ishigure, K.

1986-01-01

A number of reactions takes place concurrently when aqueous iodide solution is subjected to radiation field. In order to help analyze this complicated radiation effect measurements of rate constants were undertaken for several important reactions. One of these concerns reduction of hypoiodous acid by hydrogen peroxide. For this reaction catalytic effect was found to be significant, and old rate data was revised. Measurements on reactions involving radicals were carried out by use of pulse radiolysis technique, which also include reexamination of results by previous workers. The reactions studied are (1) oxidation of iodide ion by hydroxyl radical (2) recombination reactions of atomic iodine and diiodide ion and (3) reduction of atomic and molecular iodine either by superoxide ion or by hydroperoxyl radical

Iodide uptake by negatively charged clay interlayers?

International Nuclear Information System (INIS)

Miller, Andrew; Kruichak, Jessica; Mills, Melissa; Wang, Yifeng

2015-01-01

Understanding iodide interactions with clay minerals is critical to quantifying risk associated with nuclear waste disposal. Current thought assumes that iodide does not interact directly with clay minerals due to electrical repulsion between the iodide and the negatively charged clay layers. However, a growing body of work indicates a weak interaction between iodide and clays. The goal of this contribution is to report a conceptual model for iodide interaction with clays by considering clay mineral structures and emergent behaviors of chemical species in confined spaces. To approach the problem, a suite of clay minerals was used with varying degrees of isomorphic substitution, chemical composition, and mineral structure. Iodide uptake experiments were completed with each of these minerals in a range of swamping electrolyte identities (NaCl, NaBr, KCl) and concentrations. Iodide uptake behaviors form distinct trends with cation exchange capacity and mineral structure. These trends change substantially with electrolyte composition and concentration, but do not appear to be affected by solution pH. The experimental results suggest that iodide may directly interact with clays by forming ion-pairs (e.g., NaI (aq) ) which may concentrate within the interlayer space as well as the thin areas surrounding the clay particle where water behavior is more structured relative to bulk water. Ion pairing and iodide concentration in these zones is probably driven by the reduced dielectric constant of water in confined space and by the relatively high polarizability of the iodide species. - Highlights: • Iodide sorption experiments were completed with a diverse array of clay minerals. • Iodide uptake trended with CEC and swamping electrolyte identity and concentration. • Results can be explained by considering the formation of ion pairs in clay interlayers

A new technique for pumping hydrogen gas

Science.gov (United States)

Friedman, I.; Hardcastle, K.

1970-01-01

A system for pumping hydrogen gas without isotopic fractionation has been developed. The pump contains uranium metal, which when heated to about 80??C reacts with hydrogen to form UH3. The UH3 is heated to above 500??C to decompose the hydride and regenerate the hydrogen. ?? 1970.

Kinetics of Platinum-Catalyzed Decomposition of Hydrogen Peroxide

Science.gov (United States)

Vetter, Tiffany A.; Colombo, D. Philip, Jr.

2003-07-01

CIBA Vision Corporation markets a contact lens cleaning system that consists of an AOSEPT disinfectant solution and an AOSEPT lens cup. The disinfectant is a buffered 3.0% m/v hydrogen peroxide solution and the cup includes a platinum-coated AOSEPT disc. The hydrogen peroxide disinfects by killing bacteria, fungi, and viruses found on the contact lenses. Because the concentration of hydrogen peroxide needed to disinfect is irritating to eyes, the hydrogen peroxide needs to be neutralized, or decomposed, before the contact lenses can be used again. A general chemistry experiment is described where the kinetics of the catalyzed decomposition of the hydrogen peroxide are studied by measuring the amount of oxygen generated as a function of time. The order of the reaction with respect to the hydrogen peroxide, the rate constant, and the energy of activation are determined. The integrated rate law is used to determine the time required to decompose the hydrogen peroxide to a concentration that is safe for eyes.

Balance of Plant Requirements for a Nuclear Hydrogen Plant

Energy Technology Data Exchange (ETDEWEB)

Bradley Ward

2006-04-01

This document describes the requirements for the components and systems that support the hydrogen production portion of a 600 megawatt thermal (MWt) Next Generation Nuclear Plant (NGNP). These systems, defined as the "balance-of-plant" (BOP), are essential to operate an effective hydrogen production plant. Examples of BOP items are: heat recovery and heat rejection equipment, process material transport systems (pumps, valves, piping, etc.), control systems, safety systems, waste collection and disposal systems, maintenance and repair equipment, heating, ventilation, and air conditioning (HVAC), electrical supply and distribution, and others. The requirements in this document are applicable to the two hydrogen production processes currently under consideration in the DOE Nuclear Hydrogen Initiative. These processes are the sulfur iodide (S-I) process and the high temperature electrolysis (HTE) process. At present, the other two hydrogen production process - the hybrid sulfur-iodide electrolytic process (SE) and the calcium-bromide process (Ca-Br) -are under flow sheet development and not included in this report. While some features of the balance-of-plant requirements are common to all hydrogen production processes, some details will apply only to the specific needs of individual processes.

Iodide uptake by negatively charged clay interlayers?

Science.gov (United States)

Miller, Andrew; Kruichak, Jessica; Mills, Melissa; Wang, Yifeng

2015-09-01

Understanding iodide interactions with clay minerals is critical to quantifying risk associated with nuclear waste disposal. Current thought assumes that iodide does not interact directly with clay minerals due to electrical repulsion between the iodide and the negatively charged clay layers. However, a growing body of work indicates a weak interaction between iodide and clays. The goal of this contribution is to report a conceptual model for iodide interaction with clays by considering clay mineral structures and emergent behaviors of chemical species in confined spaces. To approach the problem, a suite of clay minerals was used with varying degrees of isomorphic substitution, chemical composition, and mineral structure. Iodide uptake experiments were completed with each of these minerals in a range of swamping electrolyte identities (NaCl, NaBr, KCl) and concentrations. Iodide uptake behaviors form distinct trends with cation exchange capacity and mineral structure. These trends change substantially with electrolyte composition and concentration, but do not appear to be affected by solution pH. The experimental results suggest that iodide may directly interact with clays by forming ion-pairs (e.g., NaI(aq)) which may concentrate within the interlayer space as well as the thin areas surrounding the clay particle where water behavior is more structured relative to bulk water. Ion pairing and iodide concentration in these zones is probably driven by the reduced dielectric constant of water in confined space and by the relatively high polarizability of the iodide species. Copyright © 2015 Elsevier Ltd. All rights reserved.

Effects of Iodide and Hydrogen Peroxide on Measuring High Temperature pH in Various Lithium Borate Buffer Solutions

Energy Technology Data Exchange (ETDEWEB)

Hwang, Jae Sik; Yun, Myung Hee; Yeon, Jei Won; Song, Kyu Seok [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2008-10-15

In a reactor coolant system of nuclear power plants, the need for reliable high temperature pH electrodes has resulted from interests in the corrosion and corrosion product behaviors of the structural materials in a high temperature coolant system. In developing the electrodes for measuring the high temperature pH of aqueous solutions, it is necessary to note two major problems: the chemical stability of an electrode against other chemical impurities, and an electrode's integrity as the temperature and pressure are varied between operational extremes. Over the past decade Macdonald et al. and Danielson et al. have developed many ceramic membrane pH electrodes based on a yttrium stabilized zirconium oxide. However, there are still many experimental difficulties associated with the problems in obtaining electrochemical information across different pressure boundaries and against many kinds of chemical impurities caused by the radiolysis of water and the leakage of a fuel clad. In the present work, we investigated the effects of the environmental factors on a high temperature pH. The selected environmental factors are as follows: system pressure, and chemical species such as iodide and hydrogen peroxide ions.

Conceptual design of the HTTR-IS hydrogen production system

International Nuclear Information System (INIS)

Sakaba, Nariaki; Sato, Hiroyuki; Hara, Teruo; Kato, Ryoma; Ohashi, Kazutaka; Nishihara, Tetsuo; Kunitomi, Kazuhiko

2007-08-01

Since hydrogen produced by nuclear should be economically competitive compared with other methods in a hydrogen society, it is important to build hydrogen production system to be coupled with the reactor as a conventional chemical plant. Japan Atomic Energy Agency started the safety study to establish a new safety philosophy to meet safety requirements for non-nuclear grade hydrogen production system. Also, structural concepts with integrating functions for the Bunsen reactor and sulphuric acid decomposer were proposed to reduce construction cost of the IS process hydrogen production system. In addition, HI decomposer which enables the process condition to be eased consisting of conventional materials and technologies was studied. Moreover, technical feasibility of the HTTR-IS system in which the hydrogen production rate of 1,000 Nm 3 /h by using the supplied heat of 10 MW from the intermediate heat exchanger of the HTTR was confirmed. This paper describes the conceptual design of the HTTR-IS hydrogen production system. (author)

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...

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...

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

International Nuclear Information System (INIS)

Lecat-Guillet, N.; Ambroise, Y.

2008-01-01

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)

Analysis for iodide in groundwater by x-ray fluorescence spectrometry after collection as silver iodide on activated charcoal

International Nuclear Information System (INIS)

Howe, P.T.

1980-01-01

The report describes the determination of microgram quantities of iodide in water by X-ray fluorescence spectrometry. The iodide is concentrated by precipitation as silver iodide on activated charcoal. If a 60-mL sample is available, a concentration of 0.12 mg/L can be detected. Precision (2σ) at the 1-mg/L level is +- 0.08 mg/L. (auth)

Photodissociation of hydrogen iodide on the surface of large argon clusters: The orientation of the librational wave function and the scattering from the cluster cage

International Nuclear Information System (INIS)

Slavicek, Petr; Jungwirth, Pavel; Lewerenz, Marius; Nahler, N. Hendrik; Farnik, Michal; Buck, Udo

2004-01-01

A set of photodissociation experiments and simulations of hydrogen iodide (HI) on Ar n clusters, with an average size =139, has been carried out for different laser polarizations. The doped clusters are prepared by a pick-up process. The HI molecule is then photodissociated by a UV laser pulse and the outgoing H fragment is ionized by resonance enhanced multiphoton ionization in a (2+1) excitation scheme within the same laser pulse at the wavelength of 243 nm. The measured time-of-flight spectra are transformed into hydrogen kinetic energy distributions. They exhibit a strong fraction of caged H atoms at zero-kinetic energy and peaks at the unperturbed cage exit for both spin-orbit channels nearly independent of the polarization. At this dissociation wavelength, the bare HI molecule exhibits a strict state separation, with a parallel transition to the spin-orbit excited state and perpendicular transitions to the ground state. The experimental results have been reproduced using molecular simulation techniques. Classical molecular dynamics was used to estimate the HI dopant distribution after the pick-up procedure. Subsequently, quasi-classical molecular dynamics (Wigner trajectories approach) has been applied for the photodissociation dynamics. The following main results have been obtained: (i) The HI dopant lands on the surface of the argon cluster during the pick-up process, (ii) zero-point energy plays a dominant role for the hydrogen orientation in the ground state of HI-Ar n surface clusters, qualitatively changing the result of the photodissociation experiment upon increasing the number of argon atoms, and, finally, (iii) the scattering of hydrogen atoms from the cage which originate from different dissociation states seriously affects the experimentally measured kinetic energy distributions

Formamidinium iodide: crystal structure and phase transitions

Directory of Open Access Journals (Sweden)

Andrey A. Petrov

2017-04-01

Full Text Available At a temperature of 100 K, CH5N2+·I− (I, crystallizes in the monoclinic space group P21/c. The formamidinium cation adopts a planar symmetrical structure [the r.m.s. deviation is 0.002 Å, and the C—N bond lengths are 1.301 (7 and 1.309 (8 Å]. The iodide anion does not lie within the cation plane, but deviates from it by 0.643 (10 Å. The cation and anion of I form a tight ionic pair by a strong N—H...I hydrogen bond. In the crystal of I, the tight ionic pairs form hydrogen-bonded zigzag-like chains propagating toward [20-1] via strong N—H...I hydrogen bonds. The hydrogen-bonded chains are further packed in stacks along [100]. The thermal behaviour of I was studied by different physicochemical methods (thermogravimetry, differential scanning calorimetry and powder diffraction. Differential scanning calorimetry revealed three narrow endothermic peaks at 346, 387 and 525 K, and one broad endothermic peak at ∼605 K. The first and second peaks are related to solid–solid phase transitions, while the third and fourth peaks are attributed to the melting and decomposition of I. The enthalpies of the phase transitions at 346 and 387 K are estimated as 2.60 and 2.75 kJ mol−1, respectively. The X-ray powder diffraction data collected at different temperatures indicate the existence of I as the monoclinic (100–346 K, orthorhombic (346–387 K and cubic (387–525 K polymorphic modifications.

Decomposing the Current

DEFF Research Database (Denmark)

Hansen, Tim

The field of molecular electronics have been shown to span a huge range of properties. In an effort to extract the parameters of the system that governs these properties, a number of methods that decomposes the current have been developed. These methods function not just as tools for data...... extraction, but also serves as the foundation upon which to gain insights into the physics that governs the molecular properties. As such, the understanding of the applicability and the development of new methods to decompose the current may be a goal in it self. In this thesis we will explore some...... of these methods, and use the insights from this study to develop new methods. First, we will compare two methods that decompose the current into the transmission from a single conducting level of the molecular device, by extracting level position and broadening. In general we see that the method that relies on I...

Iodide adsorption on the surface of chemically pretreated clinoptilolite

International Nuclear Information System (INIS)

Chmielewska-Horvatova, E.; Lesny, J.

1995-01-01

The possibility to use the monoionic Ag +- form (eventually Hg +- and Hg 2+ -forms) of clinoptilolite of domestic origin for radioactive iodide elimination from waters has been studied. The capacity of the monoforms of clinoptilolite towards iodide exceeds many times that of the capacity of clinoptilolite in natural form. Due to the low solubility product of AgI, Hg 2 I 2 and HgI 2 iodides generate precipitates on the zeolite surface. Rtg analyses of the silver form of clinoptilolite after sorption of iodide demonstrate the formation of new crystals on the zeolite surface. The influence of interfering anions on the adsorption capacity of silver clinoptilolite towards iodide was investigated, too. Kinetic curves of iodide desorption from the surface of silver and mercury clinoptilolite were compared. Simultaneously, adsorption isotherms for the systems aqueous iodide solution/Ag-, Hg-clinoptilolite were determined. (author) 6 refs.; 7 figs.; 4 tabs

21 CFR 172.375 - Potassium iodide.

Science.gov (United States)

2010-04-01

... Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION Special Dietary and Nutritional Additives § 172.375 Potassium iodide. The food additive potassium iodide may be...

In Vitro Bioavailability Study of an Antiviral Compound Enisamium Iodide

OpenAIRE

Eleonore Haltner-Ukomadu; Svitlana Gureyeva; Oleksii Burmaka; Andriy Goy; Lutz Mueller; Grygorii Kostyuk; Victor Margitich

2018-01-01

An investigation into the biopharmaceutics classification and a study of the in vitro bioavailability (permeability and solubility) of the antiviral compound enisamium iodide (4-(benzylcarbamoyl)-1-methylpyridinium iodide) were carried out. The solubility of enisamium iodide was determined in four different buffers. Apparent intestinal permeability (Papp) of enisamium iodide was assessed using human colon carcinoma (Caco-2) cells at three concentrations. The solubility of enisamium iodide in ...

Flavonoid rutin increases thyroid iodide uptake in rats.

Directory of Open Access Journals (Sweden)

Carlos Frederico Lima Gonçalves

Full Text Available Thyroid iodide uptake through the sodium-iodide symporter (NIS is not only an essential step for thyroid hormones biosynthesis, but also fundamental for the diagnosis and treatment of different thyroid diseases. However, part of patients with thyroid cancer is refractory to radioiodine therapy, due to reduced ability to uptake iodide, which greatly reduces the chances of survival. Therefore, compounds able to increase thyroid iodide uptake are of great interest. It has been shown that some flavonoids are able to increase iodide uptake and NIS expression in vitro, however, data in vivo are lacking. Flavonoids are polyhydroxyphenolic compounds, found in vegetables present in human diet, and have been shown not only to modulate NIS, but also thyroperoxidase (TPO, the key enzyme in thyroid hormones biosynthesis, besides having antiproliferative effect in thyroid cancer cell lines. Therefore, we aimed to evaluate the effect of some flavonoids on thyroid iodide uptake in Wistar rats in vivo. Among the flavonoids tested, rutin was the only one able to increase thyroid iodide uptake, so we decided to evaluate the effect of this flavonoid on some aspects of thyroid hormones synthesis and metabolism. Rutin led to a slight reduction of serum T4 and T3 without changes in serum thyrotropin (TSH, and significantly increased hypothalamic, pituitary and brown adipose tissue type 2 deiodinase and decreased liver type 1 deiodinase activities. Moreover, rutin treatment increased thyroid iodide uptake probably due to the increment of NIS expression, which might be secondary to increased response to TSH, since TSH receptor expression was increased. Thus, rutin might be useful as an adjuvant in radioiodine therapy, since this flavonoid increased thyroid iodide uptake without greatly affecting thyroid function.

Potassium Iodide

Science.gov (United States)

... certain other liquids including low-fat white or chocolate milk, flat soda, orange juice, raspberry syrup, or ... Potassium iodide may cause side effects. Tell your doctor if any of these symptoms are severe or do not go away: swollen glands metallic taste in the ...

Decomposable log-linear models

DEFF Research Database (Denmark)

Eriksen, Poul Svante

can be characterized by a structured set of conditional independencies between some variables given some other variables. We term the new model class decomposable log-linear models, which is illustrated to be a much richer class than decomposable graphical models.It covers a wide range of non...... The present paper considers discrete probability models with exact computational properties. In relation to contingency tables this means closed form expressions of the maksimum likelihood estimate and its distribution. The model class includes what is known as decomposable graphicalmodels, which......-hierarchical models, models with structural zeroes, models described by quasi independence and models for level merging. Also, they have a very natural interpretation as they may be formulated by a structured set of conditional independencies between two events given some other event. In relation to contingency...

Prevention of organic iodide formation in BWR's

International Nuclear Information System (INIS)

Karjunen, T.; Laitinen, T.; Piippo, J.; Sirkiae, P.

1996-01-01

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

Kinetic method for determination of iodide ion ultramicroamounts. Kineticheskij sposob opredeleniya ul'tramikrokolichestv iodid-ionov

Energy Technology Data Exchange (ETDEWEB)

Barkauskas, Yu K; Ramanauskas, Eh I

1980-04-03

A kinetic method for iodides ultramicroamount determination from their catalytic effect on oxidation of malachite green with chloramine B in the presence of acetone at pH 5.78+-0.3 is developed. The induction period of the reaction is determined from a change in the redox potential of the system. The induction period is proportional to the iodides concentration. Determination limit of iodides is equal to 4 ..mu..g iodide per 100 l of solution. More than 10/sup 5/-multiple amounts of K/sup +/, Na/sup +/, NH/sub 4//sup +/, Ba/sup 2 +/, Al/sup 3 +/, Cu/sup 2 +/, Mg/sup 2 +/, SO/sub 4//sup 2 -/, Cl/sup -/, MoO/sub 4//sup 2 -/, NO/sub 3//sup -/, ClO/sub 3//sup -/, IO/sub 3//sup -/, IO/sub 4//sup -/, ClO/sub 4//sup -/, BrO/sub 3//sup -/; 10/sup 5/-10/sup 3/-multiple amounts of Cr/sup 3 +/, Fe/sup 3 +/, Sn/sup 2 +/, S/sup 2 -/, MnO/sub 4//sup -/, NO/sub 2//sup -/ etc. do not interfere with the determination, while 10-multiple amounts of SCN, 0.2-multiple quantities of Ag/sup +/, Hg/sub 2//sup 2 +/ do.

Hydrogen producing method and device therefor

International Nuclear Information System (INIS)

Iwamura, Yasuhiro; Ito, Takehiko; Goto, Nobuo; Toyota, Ichiro; Tonegawa, Hiroshi.

1997-01-01

The present invention concerns a process for producing hydrogen from water by utilizing a γ · X ray radiation source such as spent nuclear fuels. Hydrogen is formed from water by combining a scintillator which uses a γ · X ray radiation source as an energy source to emit UV light and an optical catalyst or an optical catalyst electrode which undergoes UV light to decompose water into hydrogen and oxygen. The present invention provides a method of effectively using spent fuel assemblies which have not been used at present and capable of converting them into hydrogen as storable chemical energy. (N.H.)

In Vitro Bioavailability Study of an Antiviral Compound Enisamium Iodide

Directory of Open Access Journals (Sweden)

Eleonore Haltner-Ukomadu

2018-01-01

Full Text Available An investigation into the biopharmaceutics classification and a study of the in vitro bioavailability (permeability and solubility of the antiviral compound enisamium iodide (4-(benzylcarbamoyl-1-methylpyridinium iodide were carried out. The solubility of enisamium iodide was determined in four different buffers. Apparent intestinal permeability (Papp of enisamium iodide was assessed using human colon carcinoma (Caco-2 cells at three concentrations. The solubility of enisamium iodide in four buffer solutions from pH 1.2 to 7.5 is about 60 mg/mL at 25 °C, and ranges from 130 to 150 mg/mL at 37 °C, depending on the pH. Based on these results, enisamium iodide can be classified as highly soluble. Enisamium iodide demonstrated low permeability in Caco-2 experiments in all tested concentrations of 10–100 μM with permeability coefficients between 0.2 × 10−6 cm s−1 and 0.3 × 10−6 cm s−1. These results indicate that enisamium iodide belongs to class III of the Biopharmaceutics Classification System (BCS due to its high solubility and low permeability. The bioavailability of enisamium iodide needs to be confirmed in animal and human studies.

Aqueous-gas phase partitioning and hydrolysis of organic iodides

International Nuclear Information System (INIS)

Glowa, G.A.; Wren, J.C.

2003-01-01

The volatility and decomposition of organic iodides in a reactor containment building are important parameters to consider when assessing the potential consequences of a nuclear reactor accident. However, there are few experimental data available for the volatilities (often reported as partition coefficients) or few rate constants regarding the decomposition (via hydrolysis) of organic iodides. The partition coefficients and hydrolysis rate constants of eight organic iodides, having a range of molecular structures, have been measured in the current studies. This data, and data accumulated in the literature, have been reviewed and discussed to provide guidelines for appropriate organization of organic iodides for the purpose of modelling iodine behaviour under postulated nuclear reactor accident conditions. After assessment of the partition coefficients and their temperature dependences of many classes of organic compounds, it was found that organic iodides could be divided into two categories based upon their volatility relative to molecular iodine. Similarly, hydrolysis rates and their temperature dependences are assigned to the two categories of organic iodides. (author)

Silver iodide sodalite for "1"2"9I immobilisation

International Nuclear Information System (INIS)

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

2016-01-01

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, Ag_4Al_3Si_3O_1_2I, 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. - Highlights: • Dense AgI sodalite has been produced by hot isostatic pressing. • The stoichiometry of AgI sodalite has been confirmed by scanning electron microscopy. • Good I immobilisation in AgI sodalite exposed to water containing Cu or Ni metal powders was determined. • AgI sodalite exposed to water containing Fe powders decomposed and released significant quantities of iodine.

Linking loss of sodium-iodide symporter expression to DNA damage

Energy Technology Data Exchange (ETDEWEB)

Lyckesvärd, Madeleine Nordén [Sahlgrenska Cancer Center, University of Gothenburg, Göteborg (Sweden); Department of Medical Chemistry and Cell Biology, University of Gothenburg, Göteborg (Sweden); Kapoor, Nirmal [Department of Medical Chemistry and Cell Biology, University of Gothenburg, Göteborg (Sweden); Ingeson-Carlsson, Camilla; Carlsson, Therese [Sahlgrenska Cancer Center, University of Gothenburg, Göteborg (Sweden); Department of Medical Chemistry and Cell Biology, University of Gothenburg, Göteborg (Sweden); Karlsson, Jan-Olof [Department of Medical Chemistry and Cell Biology, University of Gothenburg, Göteborg (Sweden); Postgård, Per; Himmelman, Jakob; Forssell-Aronsson, Eva [Department of Radiation Physics, University of Gothenburg, Göteborg (Sweden); Hammarsten, Ola [Department of Clinical Chemistry, University of Gothenburg, Göteborg (Sweden); Nilsson, Mikael, E-mail: mikael.nilsson@gu.se [Sahlgrenska Cancer Center, University of Gothenburg, Göteborg (Sweden); Department of Medical Chemistry and Cell Biology, University of Gothenburg, Göteborg (Sweden)

2016-05-15

Radiotherapy of thyroid cancer with I-131 is abrogated by inherent loss of radioiodine uptake due to loss of sodium iodide symporter (NIS) expression in poorly differentiated tumor cells. It is also known that ionizing radiation per se down-regulates NIS (the stunning effect), but the mechanism is unknown. Here we investigated whether loss of NIS-mediated iodide transport may be elicited by DNA damage. Calicheamicin, a fungal toxin that specifically cleaves double-stranded DNA, induced a full scale DNA damage response mediated by the ataxia-telangiectasia mutated (ATM) kinase in quiescent normal thyrocytes. At sublethal concentrations (<1 nM) calicheamicin blocked NIS mRNA expression and transepithelial iodide transport as stimulated by thyrotropin; loss of function occurred at a much faster rate than after I-131 irradiation. KU-55933, a selective ATM kinase inhibitor, partly rescued NIS expression and iodide transport in DNA-damaged cells. Prolonged ATM inhibition in healthy cells also repressed NIS-mediated iodide transport. ATM-dependent loss of iodide transport was counteracted by IGF-1. Together, these findings indicate that NIS, the major iodide transporter of the thyroid gland, is susceptible to DNA damage involving ATM-mediated mechanisms. This uncovers novel means of poor radioiodine uptake in thyroid cells subjected to extrinsic or intrinsic genotoxic stress. - Highlights: • DNA damage inhibits polarized iodide transport in normal thyroid cells. • Down-regulation of NIS expression is mediated by activation of the ATM kinase. • Long-term ATM inhibition also represses NIS-mediated iodide transport. • IGF-1 rescues NIS expression and iodide transport in DNA-damaged cells.

Linking loss of sodium-iodide symporter expression to DNA damage

International Nuclear Information System (INIS)

Lyckesvärd, Madeleine Nordén; Kapoor, Nirmal; Ingeson-Carlsson, Camilla; Carlsson, Therese; Karlsson, Jan-Olof; Postgård, Per; Himmelman, Jakob; Forssell-Aronsson, Eva; Hammarsten, Ola; Nilsson, Mikael

2016-01-01

Radiotherapy of thyroid cancer with I-131 is abrogated by inherent loss of radioiodine uptake due to loss of sodium iodide symporter (NIS) expression in poorly differentiated tumor cells. It is also known that ionizing radiation per se down-regulates NIS (the stunning effect), but the mechanism is unknown. Here we investigated whether loss of NIS-mediated iodide transport may be elicited by DNA damage. Calicheamicin, a fungal toxin that specifically cleaves double-stranded DNA, induced a full scale DNA damage response mediated by the ataxia-telangiectasia mutated (ATM) kinase in quiescent normal thyrocytes. At sublethal concentrations (<1 nM) calicheamicin blocked NIS mRNA expression and transepithelial iodide transport as stimulated by thyrotropin; loss of function occurred at a much faster rate than after I-131 irradiation. KU-55933, a selective ATM kinase inhibitor, partly rescued NIS expression and iodide transport in DNA-damaged cells. Prolonged ATM inhibition in healthy cells also repressed NIS-mediated iodide transport. ATM-dependent loss of iodide transport was counteracted by IGF-1. Together, these findings indicate that NIS, the major iodide transporter of the thyroid gland, is susceptible to DNA damage involving ATM-mediated mechanisms. This uncovers novel means of poor radioiodine uptake in thyroid cells subjected to extrinsic or intrinsic genotoxic stress. - Highlights: • DNA damage inhibits polarized iodide transport in normal thyroid cells. • Down-regulation of NIS expression is mediated by activation of the ATM kinase. • Long-term ATM inhibition also represses NIS-mediated iodide transport. • IGF-1 rescues NIS expression and iodide transport in DNA-damaged cells.

Thermal decomposition of silane to form hydrogenated amorphous Si

Science.gov (United States)

Strongin, M.; Ghosh, A.K.; Wiesmann, H.J.; Rock, E.B.; Lutz, H.A. III

Hydrogenated amorphous silicon is produced by thermally decomposing silane (SiH/sub 4/) or other gases comprising H and Si, at elevated temperatures of about 1700 to 2300/sup 0/C, in a vacuum of about 10/sup -8/ to 10/sup -4/ torr. A gaseous mixture is formed of atomic hydrogen and atomic silicon. The gaseous mixture is deposited onto a substrate to form hydrogenated amorphous silicon.

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.

Chemical storage of hydrogen in few-layer graphene

Science.gov (United States)

Subrahmanyam, K. S.; Kumar, Prashant; Maitra, Urmimala; Govindaraj, A.; Hembram, K. P. S. S.; Waghmare, Umesh V.; Rao, C. N. R.

2011-01-01

Birch reduction of few-layer graphene samples gives rise to hydrogenated samples containing up to 5 wt % of hydrogen. Spectroscopic studies reveal the presence of sp3 C-H bonds in the hydrogenated graphenes. They, however, decompose readily on heating to 500 °C or on irradiation with UV or laser radiation releasing all the hydrogen, thereby demonstrating the possible use of few-layer graphene for chemical storage of hydrogen. First-principles calculations throw light on the mechanism of dehydrogenation that appears to involve a significant reconstruction and relaxation of the lattice. PMID:21282617

Safety considerations for continuous hydrogen production test apparatus with capacity of 50 N-litter hydrogen per hour

International Nuclear Information System (INIS)

Onuki, Kaoru; Akino, Norio; Shimizu, Saburo; Nakajima, Hayato; Higashi, Shunichi; Kubo, Shinji

2001-03-01

Since the thermochemical hydrogen production Iodine-Sulfur process decomposes water into hydrogen and oxygen using toxic chemicals such as sulfuric acid, iodine and hydriodic acid, safety considerations are very important in its research and development. Therefore, before construction of continuous hydrogen production test apparatus with capacity of 50 N-litter hydrogen per hour, comprehensive safety considerations were carried out to examine the design and construction works of the test apparatus, and the experimental plans using the apparatus. Emphasis was given on the safety considerations on prevention of breakage of glasswares and presumable abnormalities, accidents and their countermeasures. This report summarizes the results of the considerations. (author)

Decomposability queueing and computer system applications

CERN Document Server

Courtois, P J

1977-01-01

Decomposability: Queueing and Computer System Applications presents a set of powerful methods for systems analysis. This 10-chapter text covers the theory of nearly completely decomposable systems upon which specific analytic methods are based.The first chapters deal with some of the basic elements of a theory of nearly completely decomposable stochastic matrices, including the Simon-Ando theorems and the perturbation theory. The succeeding chapters are devoted to the analysis of stochastic queuing networks that appear as a type of key model. These chapters also discuss congestion problems in

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.

Kinetics of [123I]iodide uptake and discharge by perchlorate in studies of inhibition of iodide binding by antithyroid drugs

International Nuclear Information System (INIS)

McCruden, D.C.; Connell, J.M.C.; Alexander, W.D.; Hilditch, T.E.

1985-01-01

Thyroidal binding of iodide was studied by kinetic analysis of [ 123 ]iodide uptake and its discharge by perchlorate in 80 hyperthyroid subjects receiving antithyroid drug therapy. Five dosage regimens ranging from 5 mg carbimazole twice daily to 15 mg methimazole twice daily were studied. Binding inhibition was estimated at 5-7 h after drug as an index of the mean effect of the 12 hourly regimen. In all cases, except one in the lowest dose group, binding was found to be markedly reduced with mean binding rates ranging from 0.002 to 0.020 min -1 (normal > 0.15 min -1 ). The net clearance of iodide in the lowest dose group was reduced to a mean value near the upper limit of the euthyroid range, whereas in the highest dose group it lay at the lower limit of the euthyroid range. These results were reflected in the serum thyroid hormone response. There was a reducing incidence of inadequate control of hyperthyroidism and an increasing incidence of hypothyroidism with increasing thiourylene dose. The exit rate constant of free iodide for the various doses showed values from 0.048 to 0.055 min -1 . Correpsonding mean values for the discharge rate constant after perchlorate were 0.087 to 0.105 min -1 . This suggests that perchlorate increases the rate of iodide release from the thyroid gland. Studies at a later interval after drug (12-14 h) showed no change in discharge rate constant. This leads to the conclusion that perchlorate may further inhibit iodide binding in subjects receiving antithyroid drug therapy. (author)

Flavonoids, Thyroid Iodide Uptake and Thyroid Cancer-A Review.

Science.gov (United States)

Gonçalves, Carlos F L; de Freitas, Mariana L; Ferreira, Andrea C F

2017-06-12

Thyroid cancer is the most common malignant tumor of the endocrine system and the incidence has been increasing in recent years. In a great part of the differentiated carcinomas, thyrocytes are capable of uptaking iodide. In these cases, the main therapeutic approach includes thyroidectomy followed by ablative therapy with radioiodine. However, in part of the patients, the capacity to concentrate iodide is lost due to down-regulation of the sodium-iodide symporter (NIS), the protein responsible for transporting iodide into the thyrocytes. Thus, therapy with radioiodide becomes ineffective, limiting therapeutic options and reducing the life expectancy of the patient. Excessive ingestion of some flavonoids has been associated with thyroid dysfunction and goiter. Nevertheless, studies have shown that some flavonoids can be beneficial for thyroid cancer, by reducing cell proliferation and increasing cell death, besides increasing NIS mRNA levels and iodide uptake. Recent data show that the flavonoids apingenin and rutin are capable of increasing NIS function and expression in vivo. Herein we review literature data regarding the effect of flavonoids on thyroid cancer, besides the effect of these compounds on the expression and function of the sodium-iodide symporter. We will also discuss the possibility of using flavonoids as adjuvants for therapy of thyroid cancer.

Flavonoids, Thyroid Iodide Uptake and Thyroid Cancer—A Review

Science.gov (United States)

Gonçalves, Carlos F. L.; de Freitas, Mariana L.; Ferreira, Andrea C. F.

2017-01-01

Thyroid cancer is the most common malignant tumor of the endocrine system and the incidence has been increasing in recent years. In a great part of the differentiated carcinomas, thyrocytes are capable of uptaking iodide. In these cases, the main therapeutic approach includes thyroidectomy followed by ablative therapy with radioiodine. However, in part of the patients, the capacity to concentrate iodide is lost due to down-regulation of the sodium-iodide symporter (NIS), the protein responsible for transporting iodide into the thyrocytes. Thus, therapy with radioiodide becomes ineffective, limiting therapeutic options and reducing the life expectancy of the patient. Excessive ingestion of some flavonoids has been associated with thyroid dysfunction and goiter. Nevertheless, studies have shown that some flavonoids can be beneficial for thyroid cancer, by reducing cell proliferation and increasing cell death, besides increasing NIS mRNA levels and iodide uptake. Recent data show that the flavonoids apingenin and rutin are capable of increasing NIS function and expression in vivo. Herein we review literature data regarding the effect of flavonoids on thyroid cancer, besides the effect of these compounds on the expression and function of the sodium-iodide symporter. We will also discuss the possibility of using flavonoids as adjuvants for therapy of thyroid cancer. PMID:28604619

Photoluminescence Enhancement in Formamidinium Lead Iodide Thin Films

NARCIS (Netherlands)

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

2016-01-01

Formamidinium lead iodide (FAPbI(3)) has a broader absorption spectrum and better thermal stability than the most famous methylammonium lead iodide, thus exhibiting great potential for photovoltaic applications. In this report, the light-induced photoluminescence (PL) evolution in FAPbI(3) thin

Research on solubility characteristics of gaseous methyl iodide

International Nuclear Information System (INIS)

Zhou Yanmin; Sun Zhongning; Gu Haifeng; Wang Junlong

2014-01-01

With the deionized water as the absorbent, the solubility characteristics of the gaseous methyl iodide were studied under different temperature and pressure conditions, using a dynamic measuring method. The results show that within the range of experiment parameters, namely temperature is below 80℃ and pressure is lower than 0.3 MPa, the physical dissolution process of gaseous methyl iodide in water obeys Henry's law. The solubility coefficient under different temperature and pressure conditions was calculated based on the measurement results. Further research indicates that at atmospheric pressure, the solubility coefficient of methyl iodide in water decreases exponentially with the increase of temperature. While the pressure changes from 0.1 MPa to 0.3 MPa with equal interval, the solubility coefficient also increases linearly. The variation of the solubility coefficient with temperature under different pressure conditions all decreases exponentially. An equation is given to calculate the solubility coefficient of methyl iodide under different pressure and temperature conditions. (authors)

Kinetic method for determination of iodide ion ultramicroamounts

International Nuclear Information System (INIS)

Barkauskas, Yu.K.; Ramanauskas, Eh.I.

1980-01-01

A kinetic method for iodides ultramicroamount determination from their catalytic effect on oxidation of malachite green with chloramine B in the presence of acetone at pH 5.78+-0.3 is developed. The induction period of the reaction is determined from a change in the redox potential of the system. The induction period is proportional to the iodides concentration. Determination limit of iodides is equal to 4 μg iodide per 100 l of solution. More than 10 5 -multiple amounts of K + , Na + , NH 4+ , Ba 2 + , Al 3 + , Cu 2 + , Mg 2 + , SO 4 2 - , Cl - , MoO 4 2 - , NO 3- , ClO 3- , IO 3- , IO 4- , ClO 4- , BrO 3- ; 10 5 -10 3 -multiple amounts of Cr 3 + , Fe 3 + , Sn 2 + , S 2 - , MnO 4- , NO 2- etc. do not interfere with the determination, while 10-multiple amounts of SCN, 0.2-multiple quantities of Ag + , Hg 2 2 + do

Products of the reaction between methylene iodide and tertiary arsines

International Nuclear Information System (INIS)

Gigauri, R.D.; Arabuli, L.G.; Machaidze, Z.I.; Rusiya, M.Sh.

2005-01-01

Iodides of iodomethylenetrialkyl(aryl) arsonium were synthesized with high yields as a result of interaction between methylene iodide and tertiary arsines. Exchange reactions of the iodides prepared with lead(II) nitrate in water-alcohol solutions gave rise to formation of iodomethylenetrialkyl(aryl) arsonium nitrates. All the products prepared were characterized by data of elementary analysis, IR spectroscopy, conductometry and melting points measurements [ru

Technical Integration of Nuclear Hydrogen Production Technology

International Nuclear Information System (INIS)

Lee, Ki Young; Park, J. K.; Chang, J. H.

2009-04-01

These works focus on the development of attainment indices for nuclear hydrogen key technologies, the analysis of the hydrogen production process and the performance estimation for hydrogen production systems, and the assessment of the nuclear hydrogen production cost. For assessing the degree of attainments in comparison with the final goals of VHTR technologies in progress of researches, subdivided are the prerequisite items confirmed to the NHDD concepts. We developed and applied R and D quality management methodology to meet 'Development of Key Technologies for Nuclear Hydrogen' project. And we also distributed R and D QAM and R and D QAP to each teams and are in operation. The preconceptual flow diagrams of SI, HTSE, and HyS processes are introduced and their material and energy balances have been proposed. The hydrogen production thermal efficiencies of not only the SI process as a reference process but also the HTSE and HyS processes were also estimated. Technical feasibility assessments of SI, HTSE, and HyS processes have been carried out by using the pair-wise comparison and analytic hierarchy process, and it is revealed that the experts are considering the SI process as the most feasible process. The secondary helium pathway across the SI process is introduced. Dynamic simulation codes for the H2S04vaporizer, sulfuric acid and sulfur trioxide decomposers, and HI decomposer on the secondary helium pathway and for the primary and secondary sulfuric acid distillation columns, HIx solution distillation column, and preheater for HI vapor have been developed and integrated

Novel Composite Hydrogen-Permeable Membranes for Nonthermal Plasma Reactors for the Decomposition of Hydrogen Sulfide

Energy Technology Data Exchange (ETDEWEB)

Morris Argyle; John Ackerman; Suresh Muknahallipatna; Jerry Hamann; Stanislaw Legowski; Gui-Bing Zhao; Sanil John; Ji-Jun Zhang; Linna Wang

2007-09-30

The goal of this experimental project was to design and fabricate a reactor and membrane test cell to dissociate hydrogen sulfide (H{sub 2}S) in a nonthermal plasma and to recover hydrogen (H{sub 2}) through a superpermeable multi-layer membrane. Superpermeability of hydrogen atoms (H) has been reported by some researchers using membranes made of Group V transition metals (niobium, tantalum, vanadium, and their alloys), but it was not achieved at the moderate pressure conditions used in this study. However, H{sub 2}S was successfully decomposed at energy efficiencies higher than any other reports for the high H{sub 2}S concentration and moderate pressures (corresponding to high reactor throughputs) used in this study.

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.

Solid electrolyte membranes and the system to produce hydrogen from thermally decomposed water by solar energy; Taiyo energy riyo ni yoru mizu no chokusetsu netsubunkai kara no suiso seizoyo

Energy Technology Data Exchange (ETDEWEB)

Nigara, K; Watanabe, K; Kawamura, K; Kawada, T; Mizusaki, J; Ishigame, M [Tohoku University, Sendai (Japan). Research Institute for Scientific Measurements

1996-10-27

For conversion of solar heat to transportable energy, hydrogen production by direct thermal decomposition of water using concentrated high-temperature solar heat was studied. Water vapor is injected into the tubular target with high melting point and high oxygen permeability at high temperature while heating the target by concentrated solar heat over 2000K. Oxygen in decomposed gas is discharged through an oxygen permeable membrane to extract hydrogen. Solid electrolyte is used as one of the target materials. Oxygen gas in the high-oxygen partial pressure site changes into oxygen ion by accepting two electrons at the target surface, and returns to neutral oxygen gas in the low-oxygen partial pressure site by discharging two electrons at the surface after permeation through oxygen vacancy. In the case of n-type solid electrolyte, to obtain constant permeation of a large amount of oxygen, flow of a large amount of electrons is indispensable in the opposite direction to oxygen ion. Among [(ZrO2)(1-x)(CeO2)x](0.9)(CaO)(0.1), materials of 0.4-0.5 in x seems to be useful as the target material. 7 refs., 7 figs.

Method of removing alkyl iodides or mixtures of iodine and alkyl iodides from a gas phase and an aqueous solution phase by utilizing ion exchange resins

International Nuclear Information System (INIS)

Shimizu, Hiroshi; Mizuuchi, Noboru; Yokoyama, Fumio.

1967-01-01

Alkyl iodides and mixtures of iodine and alkyl iodides are removed from a gas phase and an aquous solution phase by using solely an anion exchange resin containing a tertiary amine or together with an anion exchange resin containing quarternary ammonium compound. The resin containing the quarternary ammonium compound is employed mainly to remove iodine, and the resin containing the tertiary amine serves mainly to remove alkyl iodides. The method can be applied to collecting a majority of the methyl iodide as well as the radioactive iodine produced in the atmosphere of a reactor in case of a fuel accident. In embodiments, it is desirable to maintain the sufficient moisture content of the anion exchange resins at a sufficient moisture level so as not to reduce the migration speed of the iodine and alkyl iodides. The iodine and alkyl iodide can be produced with high efficiency and stability independently of the relative humidity of the gas phase. In examples, a solution which consists of 20.5 mg/l of iodine and 42.2mg/l of methyl iodide flew through a column of Amberite IRA-93 alone or blended with IRA-900 at a speed of 15 /hr. respectively. The resins were able to treat 400 times their equivalent in water. (Iwakiri, K.)

Fullerene hydride - A potential hydrogen storage material

International Nuclear Information System (INIS)

Nai Xing Wang; Jun Ping Zhang; An Guang Yu; Yun Xu Yang; Wu Wei Wang; Rui long Sheng; Jia Zhao

2005-01-01

Hydrogen, as a clean, convenient, versatile fuel source, is considered to be an ideal energy carrier in the foreseeable future. Hydrogen storage must be solved in using of hydrogen energy. To date, much effort has been put into storage of hydrogen including physical storage via compression or liquefaction, chemical storage in hydrogen carriers, metal hydrides and gas-on-solid adsorption. But no one satisfies all of the efficiency, size, weight, cost and safety requirements for transportation or utility use. C 60 H 36 , firstly synthesized by the method of the Birch reduction, was loaded with 4.8 wt% hydrogen indicating [60]fullerene might be as a potential hydrogen storage material. If a 100% conversion of C 60 H 36 is achieved, 18 moles of H 2 gas would be liberated from each mole of fullerene hydride. Pure C 60 H 36 is very stable below 500 C under nitrogen atmosphere and it releases hydrogen accompanying by other hydrocarbons under high temperature. But C 60 H 36 can be decomposed to generate H 2 under effective catalyst. We have reported that hydrogen can be produced catalytically from C 60 H 36 by Vasks's compound (IrCl(CO)(PPh 3 ) 2 ) under mild conditions. (RhCl(CO)(PPh 3 ) 2 ) having similar structure to (IrCl(CO)(PPh 3 ) 2 ), was also examined for thermal dehydrogenation of C 60 H 36 ; but it showed low catalytic activity. To search better catalyst, palladium carbon (Pd/C) and platinum carbon (Pt/C) catalysts, which were known for catalytic hydrogenation of aromatic compounds, were tried and good results were obtained. A very big peak of hydrogen appeared at δ=5.2 ppm in 1 H NMR spectrum based on Evans'work (fig 1) at 100 C over a Pd/C catalyst for 16 hours. It is shown that hydrogen can be produced from C 60 H 36 using a catalytic amount of Pd/C. Comparing with Pd/C, Pt/C catalyst showed lower activity. The high cost and limited availability of Vaska's compounds, Pd and Pt make it advantageous to develop less expensive catalysts for our process based on

Laccase-catalyzed oxidation of iodide and formation of organically bound iodine in soils.

Science.gov (United States)

Seki, Miharu; Oikawa, Jun-ichi; Taguchi, Taro; Ohnuki, Toshihiko; Muramatsu, Yasuyuki; Sakamoto, Kazunori; Amachi, Seigo

2013-01-02

Laccase oxidizes iodide to molecular iodine or hypoiodous acid, both of which are easily incorporated into natural soil organic matter. In this study, iodide sorption and laccase activity in 2 types of Japanese soil were determined under various experimental conditions to evaluate possible involvement of this enzyme in the sorption of iodide. Batch sorption experiment using radioactive iodide tracer ((125)I(-)) revealed that the sorption was significantly inhibited by autoclaving (121 °C, 40 min), heat treatment (80 and 100 °C, 10 min), γ-irradiation (30 kGy), N(2) gas flushing, and addition of reducing agents and general laccase inhibitors (KCN and NaN(3)). Interestingly, very similar tendency of inhibition was observed in soil laccase activity, which was determined using 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonate) (ABTS) as a substrate. The partition coefficient (K(d): mL g(-1)) for iodide and specific activity of laccase in soils (Unit g(-1)) showed significant positive correlation in both soil samples. Addition of a bacterial laccase with an iodide-oxidizing activity to the soils strongly enhanced the sorption of iodide. Furthermore, the enzyme addition partially restored iodide sorption capacity of the autoclaved soil samples. These results suggest that microbial laccase is involved in iodide sorption on soils through the oxidation of iodide.

Colorimetric sensing of iodide based on triazole-acetamide functionalized gold nanoparticles

International Nuclear Information System (INIS)

Lee, I-Lin; Sung, Yi-Ming; Wu, Shu-Pao; Wu, Chien-Hou

2014-01-01

We have modified gold nanoparticles (AuNPs) with triazole acetamide to obtain a material for the sensitive and selective colorimetric determination of iodide. The functionalized AuNPs were prepared by a reductive single chemical step using a Cu(I)-catalyzed click reaction. The presence of iodide ions induces the aggregation of these AuNPs and results in a color change from wine-red to purple. The iodide-induced aggregation can be detected visually with bare eyes, but also by photometry. The detection limit is as low as 15 nM. The method displays excellent selectivity for iodide over other anions due to the selective interaction with the amido groups of the triazole. The method was applied to the determination of iodide in spiked lake waters. (author)

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 valuemicroemulsion. 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.

Study of the Mo(VI) catalytic response in the oxidation of iodide by hydrogen peroxide using a monosegmented continuous-flow system

International Nuclear Information System (INIS)

Andrade, J.C. de; Eiras, S.P.; Bruns, R.E.

1991-01-01

Fractional factorial, modified simplex and response surface studies of the Mo(VI)-catalysed and non-catalysed oxidation of iodide by hydrogen peroxide in acidic medium were executed using a monosegmented continuous-flow system (MCFS). As this reaction is commonly used for the spectrophotometric catalytic determination of Mo(VI), the behaviour of the analytically useful response, ΔA, the difference of the average absorbance values of the Mo(VI)-catalysed and non-catalysed reactions, was studied over a large range of experimental conditions. The effects of simultaneous changes in the sample flow-rate, the H 2 SO 4 , KI and H 2 O 2 concentrations and the reaction time on the signals were measured. The optimum concentrations found using MCFS are 0.0665, 0.1528 and 0.0041 M for H 2 SO 4 , KI and H 2 O 2 , respectively. Rigorous control of the acid concentration is essential to maintain the sensitivity of the analytical signal for operating conditions close to the optimum values recommended here. On the other hand, the ΔA values are much less sensitive to variations in the H 2 O 2 concentration. Increasing KI concentrations can improve the sensitivity but can also cause baseline instability. The response surface is convenient for visualizing the overall behaviour of the system for the experimental control values investigated. (author). 24 refs.; 3 figs.; 1 tab

Parametric Study on the Organic Iodide Behavior during a Severe Accident

International Nuclear Information System (INIS)

Ryu, Myung Hyun; Kim, Han Chul; Kim, Do Sam

2011-01-01

Iodine is a major contributor to the potential health risk for the public following a severe accident from a nuclear power plant. Most of metal-iodides, the major form of iodine that enters the containment, can be readily dissolved in the sump water and result in iodide ions. These will be oxidized to form volatile I 2 through a large number of reactions such as radiolysis and hydrolysis. The organic radicals, made from organics such as paint in the sump water, react with iodine to produce organic iodides. Volatile iodine moves from the sump water to the atmosphere mainly by diffusion and natural convection, and react with surfaces and air radiolysis products (ARPs). Painted surfaces act as a sink for I 2 and as a source for organic iodides through adsorption and desorption. ARPs react with I 2 to form iodine oxides, which leads to the decrease of I 2 and organic iodides. Among the large number of iodine species, organic iodides have been extensively studied recently due to their volatility and very low retention. Qualified tools for modeling these phenomena have been developed and validated by several experiments such as EPICUR, PARIS and OECD-BIP. While mechanistic codes model a large number of reactions and species, semiempirical codes such as IODE or IMOD treat major ones. KINS developed a simple iodine model, RAIM (Radio-active iodine chemistry model), based on the IMOD methodology in order to deal with organic iodides conveniently, coupling with an integrated severe-accident analysis code. There are a number of mechanisms that affect the behavior of organic iodides. In this study, effects of pH of the aqueous phase, temperature, radiation dose rate, surface area of organic paints, initial iodine loads that are known to be important to organic iodide formation were studied analytically with RAIM, and also theoretically

Parametric Study on the Organic Iodide Behavior during a Severe Accident

Energy Technology Data Exchange (ETDEWEB)

Ryu, Myung Hyun; Kim, Han Chul; Kim, Do Sam [Korea Institute of Nuclear Safety, Daejeon (Korea, Republic of)

2011-10-15

Iodine is a major contributor to the potential health risk for the public following a severe accident from a nuclear power plant. Most of metal-iodides, the major form of iodine that enters the containment, can be readily dissolved in the sump water and result in iodide ions. These will be oxidized to form volatile I{sub 2} through a large number of reactions such as radiolysis and hydrolysis. The organic radicals, made from organics such as paint in the sump water, react with iodine to produce organic iodides. Volatile iodine moves from the sump water to the atmosphere mainly by diffusion and natural convection, and react with surfaces and air radiolysis products (ARPs). Painted surfaces act as a sink for I{sub 2} and as a source for organic iodides through adsorption and desorption. ARPs react with I{sub 2} to form iodine oxides, which leads to the decrease of I{sub 2} and organic iodides. Among the large number of iodine species, organic iodides have been extensively studied recently due to their volatility and very low retention. Qualified tools for modeling these phenomena have been developed and validated by several experiments such as EPICUR, PARIS and OECD-BIP. While mechanistic codes model a large number of reactions and species, semiempirical codes such as IODE or IMOD treat major ones. KINS developed a simple iodine model, RAIM (Radio-active iodine chemistry model), based on the IMOD methodology in order to deal with organic iodides conveniently, coupling with an integrated severe-accident analysis code. There are a number of mechanisms that affect the behavior of organic iodides. In this study, effects of pH of the aqueous phase, temperature, radiation dose rate, surface area of organic paints, initial iodine loads that are known to be important to organic iodide formation were studied analytically with RAIM, and also theoretically

Thyroid iodide compartments and their implication in the rat thyroid iodine organification

International Nuclear Information System (INIS)

Bastiani, P.; Simon, C.

1982-01-01

To estimate the relative participation of transported and intrathyroidally generated iodide (internal iodide) in the iodination of newly synthesized and preexisting thyroglobulin (Tg) in the rat thyroid, the specific radioactivities (SRAs) of thyroid iodide, Tg, lysosomal iodine, and plasma hormones were followed for 92 h after radioactive iodide injection in intact or hypophysectomized rats. In control rats, the SRA of Tg and lysosomal iodine reached a maximum at 12 h. However, the SRA of lysosomal iodide was always smaller than that of Tg. In contrast, the SRA of hormonal iodide attained a maximum at 48 h. Thus, newly labeled iodine is endocytosed and mixed inside the lysosomes with older previously iodinated molecules; hormone secretion is mainly due to old labeled iodine (i.e. iodine with a high SRA from 48-96 h). These results are consistent with the presence of least two Tg compartments, with different turnover rates and hormone contents. On the other hand, in hypophysectomized rats, the SRA of Tg, lysosomes, and hormones showed only one maximum, at 24 h. Furthermore, the SRAs of Tg and lysosomes were similar at each time interval. It is inferred that in such rats, the old labeled iodine compartment is strongly reduced, and that inside the lysosomes, newly labeled iodine is predominant. Since in hypophysectomized rats, the recycling of iodide is abolished, it is concluded that in normal rats: 1) transported iodide is organified mainly by direct iodination of newly synthesized Tg, independently of TSH, and 2) internal iodide is organified mainly by delayed iodination of preexisting Tg, this process being TSH dependent

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.

High temperature hydrogenation of CaC6

International Nuclear Information System (INIS)

Srinivas, G.; Howard, C.A.; Skipper, N.T.; Bennington, S.M.; Ellerby, M.

2009-01-01

The structure and superconducting properties of high temperature hydrogenated calcium-graphite intercalation compound, CaC 6 have been investigated using room temperature X-ray diffraction, and temperature and field dependence of magnetisation. It is found that the hydrogenation can only decompose the CaC 6 phase, and generate a mixture of CaH 2 and graphite as the final compound. The hydrogenation of CaC 6 also reveals a degradation of its superconducting properties. The experimental results are discussed in detail and it is found that the formation of stable CaH 2 and deintercalation are the main source for observed phase separation and suppression in superconductivity.

Method of decomposing treatment for radioactive organic phosphate wastes

International Nuclear Information System (INIS)

Uki, Kazuo; Ichihashi, Toshio; Hasegawa, Akira; Sato, Tatsuaki

1985-01-01

Purpose: To decompose the organic phosphoric-acid ester wastes containing radioactive material, which is produced from spent fuel reprocessing facilities, into inorganic materials using a simple device, under moderate conditions and at high decomposing ratio. Method: Radioactive organic phosphate wates are oxidatively decomposed by H 2 O 2 in an aqueous phosphoric-acid solution of metal phosphate salts. Copper phosphates are used as the metal phosphate salts and the decomposed solution of the radioactive organic phosphate wastes is used as the aqueous solution of the copper phosphate. The temperature used for the oxidizing decomposition ranges from 80 to 100 0 C. (Ikeda, J.)

Determination of nanogram amounts of iodide by electrochemical isotope dilution analysis

International Nuclear Information System (INIS)

Gabrielsson, A.-B.; Beronius, P.

1976-01-01

A known quantity of iodide in ethanol as solvent was labelled with 131 I-and subsequently diluted with a predetermined amount of inactive iodide. Specific activities before and after the isotope dilution were established by anodically depositing small fractions of the halide in each sample on rotating silver micro electrodes and determining the activities of the electrodeposits. The lowest concentration of iodide used in any analysis was 1.10 -5 M. Further deposition studies revealed that iodide can be deposited with 1 100% current efficiency on the rotating silver micro electrode for concentration down to 2.4.10 -6 M. Electrodeposition studies for still lower concentrations have not yet been undertaken. These results suggest that amounts of iodide ion down to about 10 ng, and possibly still smaller quantitites, might be determined with the method developed. Amounts from 42 ng to 1 μg can be determined with an error of 2.5%. (T.G.)

Decomposing dynamic profit inefficiency of Belgian dairy farms

NARCIS (Netherlands)

Ang, Frederic; Lansink, Alfons Oude

2018-01-01

This paper introduces a nonparametric framework for analysing dynamic profit inefficiency and applies this to a sample of Belgian, specialised dairy farms from 1996 to 2008. Profit inefficiency is decomposed into technical and allocative inefficiency. The paper also decomposes profit inefficiency

Method to remove methyl iodide131 gas

International Nuclear Information System (INIS)

Deitz, V.R.; Blachly, C.H.

1977-01-01

A two-stage impregnation process for charcoal is presented which is to be used for radioactive iodine or methyl iodide removal from the waste gas of a nuclear reactor. In the first stage, the coal is treated at pH 10 with an aqueous mixture of a salt of iodic acid (hypoiodite, iodate, or periodate) with iodine or iodide. In the second stage, impregnation with a tertiary amine occurs. The concentrations are chosen so that the charcoal will take up between 0.5 and 4% by weight of iodine. (UWI) [de

Lactobacillus bulgaricus mutants decompose uremic toxins.

Science.gov (United States)

Bai, Yun-Huan; Jiang, Ya-Fen; Jiang, Yun-Sheng

2014-06-01

We aim to obtain a probiotic strain from Lactobacillus bulgaricus by testing its capability to decompose uremic toxins to provide new intestinal bacteria for the treatment of chronic renal failure. Original L. bulgaricus was cultured with the serum of uremic patients and then mutated by physical (ultraviolet) and chemical (diethyl sulfate) methods repeatedly. Using creatinine decomposition rate as an observed index, we selected the best strains which decreased the most concentration of the creatinine. We then tested its ability to decompose urea, uric acid, serum phosphate, parathyroid hormone, and homocysteine and its genetic stability. After inductive and mutagenic treatment, DUC3-17 was selected. Its decomposition rate of creatinine, urea nitrogen, uric acid, phosphorus, parathyroid hormone, and homocysteine were 17.23%, 36.02%, 9.84%, 15.73%, 78.26%, and 12.69%, respectively. The degrading capacity was sustained over five generations. After directional induction and compound mutation, L. bulgaricus has greater capacity to decompose uremic toxins, with a stable inheritance.

A glucose bio-battery prototype based on a GDH/poly(methylene blue) bioanode and a graphite cathode with an iodide/tri-iodide redox couple.

Science.gov (United States)

Wang, Jen-Yuan; Nien, Po-Chin; Chen, Chien-Hsiao; Chen, Lin-Chi; Ho, Kuo-Chuan

2012-07-01

A glucose bio-battery prototype independent of oxygen is proposed based on a glucose dehydrogenase (GDH) bioanode and a graphite cathode with an iodide/tri-iodide redox couple. At the bioanode, a NADH electrocatalyst, poly(methylene blue) (PMB), which can be easily grown on the electrode (screen-printed carbon paste electrode, SPCE) by electrodeposition, is harnessed and engineered. We find that carboxylated multi-walled carbon nanotubes (MWCNTs) are capable of significantly increasing the deposition amount of PMB and thus enhancing the PMB's electrocatalysis of NADH oxidation and the glucose bio-battery's performance. The choice of the iodide/tri-iodide redox couple eliminates the dependence of oxygen for this bio-battery, thus enabling the bio-battery with a constant current-output feature similar to that of the solar cells. The present glucose bio-battery prototype can attain a maximum power density of 2.4 μW/cm(2) at 25 °C. Crown Copyright © 2012. Published by Elsevier Ltd. All rights reserved.

The iodine/iodide redox couple at a platinum electrode

NARCIS (Netherlands)

Dane, L.M.; Janssen, L.J.J.; Hoogland, J.G.

1968-01-01

The I/iodide redox couple was studied on Pt in 0.5M H2SO4 by measuring the impedance as a function of frequency. From these measurements, the exchange c.d. j0 was derived according to Sluyters. The dependence of j0 on the reversible potential and the I and the iodide concns. was established. By

Auger recombination in sodium iodide

Science.gov (United States)

McAllister, Andrew; Kioupakis, Emmanouil; Åberg, Daniel; Schleife, André

2014-03-01

Scintillators are an important tool used to detect high energy radiation - both in the interest of national security and in medicine. However, scintillator detectors currently suffer from lower energy resolutions than expected from basic counting statistics. This has been attributed to non-proportional light yield compared to incoming radiation, but the specific mechanism for this non-proportionality has not been identified. Auger recombination is a non-radiative process that could be contributing to the non-proportionality of scintillating materials. Auger recombination comes in two types - direct and phonon-assisted. We have used first-principles calculations to study Auger recombination in sodium iodide, a well characterized scintillating material. Our findings indicate that phonon-assisted Auger recombination is stronger in sodium iodide than direct Auger recombination. Computational resources provided by LLNL and NERSC. Funding provided by NA-22.

Studies of selected transuranium and lanthanide tri-iodides under pressure using absorption spectrophotometry

International Nuclear Information System (INIS)

Haire, R.G.; Young, J.P.; Peterson, J.R.; Tennessee Univ., Knoxville; Benedict, U.

1987-01-01

The anhydrous tri-iodides of plutonium, americium and curium under pressure have been investigated using absorption spectrophotometry. These initial studies on plutonium and curium tri-iodides together with the published data for americium tri-iodide show that the rhombohedral form of these compounds (BiI 3 -type structure) can be converted to the orthorhombic form (PuBr 3 -type structure) by applying pressure at room temperature. Absorption spectrophotometry can often differentiate between two crystallographic forms of a material and has been used in the present high-pressure studies to monitor the effects of pressure on the tri-iodides. A complication in these studies of the tri-iodides is a significant shift of their absorption edges with pressure from the near UV to the visible spectral region. With curium tri-iodide this shift causes interference with the major f-f absorption peaks and precludes identification by absorption spectrophotometry of the high pressure phase of CmI 3 . (orig.)

A selective iodide ion sensor electrode based on functionalized ZnO nanotubes.

Science.gov (United States)

Ibupoto, Zafar Hussain; Khun, Kimleang; Willander, Magnus

2013-02-04

In this research work, ZnO nanotubes were fabricated on a gold coated glass substrate through chemical etching by the aqueous chemical growth method. For the first time a nanostructure-based iodide ion selective electrode was developed. The ZnO nanotubes were functionalized with miconazole ion exchanger and the electromotive force (EMF) was measured by the potentiometric method. The iodide ion sensor exhibited a linear response over a wide range of concentrations (1 × 10-6 to 1 × 10-1 M) and excellent sensitivity of -62 ± 1 mV/decade. The detection limit of the proposed sensor was found to be 5 × 10-7 M. The effects of pH, temperature, additive, plasticizer and stabilizer on the potential response of iodide ion selective electrode were also studied. The proposed iodide ion sensor demonstrated a fast response time of less than 5 s and high selectivity against common organic and the inorganic anions. All the obtained results revealed that the iodide ion sensor based on functionalized ZnO nanotubes may be used for the detection of iodide ion in environmental water samples, pharmaceutical products and other real samples.

A Selective Iodide Ion Sensor Electrode Based on Functionalized ZnO Nanotubes

Directory of Open Access Journals (Sweden)

Magnus Willander

2013-02-01

Full Text Available In this research work, ZnO nanotubes were fabricated on a gold coated glass substrate through chemical etching by the aqueous chemical growth method. For the first time a nanostructure-based iodide ion selective electrode was developed. The ZnO nanotubes were functionalized with miconazole ion exchanger and the electromotive force (EMF was measured by the potentiometric method. The iodide ion sensor exhibited a linear response over a wide range of concentrations (1 × 10−6 to 1 × 10−1 M and excellent sensitivity of –62 ± 1 mV/decade. The detection limit of the proposed sensor was found to be 5 × 10−7 M. The effects of pH, temperature, additive, plasticizer and stabilizer on the potential response of iodide ion selective electrode were also studied. The proposed iodide ion sensor demonstrated a fast response time of less than 5 s and high selectivity against common organic and the inorganic anions. All the obtained results revealed that the iodide ion sensor based on functionalized ZnO nanotubes may be used for the detection of iodide ion in environmental water samples, pharmaceutical products and other real samples.

On conditional decomposability

Czech Academy of Sciences Publication Activity Database

Komenda, Jan; Masopust, Tomáš; van Schuppen, J. H.

2012-01-01

Roč. 61, č. 12 (2012), s. 1260-1268 ISSN 0167-6911 R&D Projects: GA ČR(CZ) GPP202/11/P028; GA ČR(CZ) GAP103/11/0517 Institutional support: RVO:67985840 Keywords : discrete-event system * coordination control * conditional decomposability Subject RIV: BA - General Mathematics Impact factor: 1.667, year: 2012 http://www.sciencedirect.com/science/article/pii/S0167691112001612

The iodide sym-porter (NIS): new perspectives in nuclear oncology

International Nuclear Information System (INIS)

Pourcher, Th.; Lindenthal, S.; Basquin, C.; Ferhat, O.; Marsault, R.; Carrier, P.; Koulibaly, M.; Bussiere, F.; Darcourt, J.

2005-01-01

The sodium iodide sym-porter (NIS) is the plasma membrane protein that mediates uptake of iodide in the thyroid and other organs such as the stomach and the salivary gland. The cloning of its cDNA allows the targeting of NIS expression into any cell using gene therapy. This enables iodide uptake and thus NIS can be used as reporter imaging for live animals. More intriguingly, this new technique has potential using radio-iodide therapy to selectively destroy tumour cells. These two approaches employ common techniques in nuclear medicine. Many experiments on cultured cells and on animals have been carried out; they established clearly the advantages of this genetically targeted radiotherapy. Recent studies employing this therapy on multiple myeloma cell lines implanted in mice or on hepato-carcinoma-bearing rats, resulted in important tumour remission. However, additional studies on NIS regulation and the use of alternative radioisotopes transported by NIS are required to further develop this promising approach. (author)

Evaluating iodide recycling inhibition as a novel molecular initiating event for thyroid axis disruption

Science.gov (United States)

The enzyme iodotyrosine deiodinase (dehalogenase, IYD) catalyzes iodide recycling and promotes iodide retention in thyroid follicular cells. Loss of function or chemical inhibition of IYD reduces available iodide for thyroid hormone synthesis, which leads to hormone insufficiency...

Electro regeneration of iodide loaded resin. Contributed Paper RD-18

International Nuclear Information System (INIS)

Kumar, Ratnesh; Kumar, T.; Sree Kumar, B.; Seshadri, K.S.; Paul, Biplob

2014-01-01

Spent resins generated in the nuclear reactor contain essentially cationic activities due to Cesium, Strontium, Cobalt, and anionic activities due to Iodide, Iodate etc with activity loading to the extent of 0.1 Cim -3 and a surface dose of the order of 5 R. It is necessary to convert the spent resin into innocuous, reusable forms. An attempt has been made to regenerate Iodide containing spent resin into OH - electrolytically by using the OH - produced at the cathode compartment of an electrolytic cell. Results show that the regeneration of the spent resin containing Iodide could be completely accomplished electrolytically more efficiently than by addition of alkali. (author)

40 CFR Table 3 to Subpart IIIii of... - Work Practice Standards-Required Actions for Liquid Mercury Spills and Accumulations and Hydrogen...

Science.gov (United States)

2010-07-01

... Actions for Liquid Mercury Spills and Accumulations and Hydrogen and Mercury Vapor Leaks 3 Table 3 to... Standards—Required Actions for Liquid Mercury Spills and Accumulations and Hydrogen and Mercury Vapor Leaks... cell back into service until the leaking equipment is repaired. 3. A decomposer or hydrogen system...

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.

Removal efficiency of radioactive methyl iodide on TEDA-impregnated activated carbons

International Nuclear Information System (INIS)

Gonzalez-Garcia, C.M.; Gonzalez, J.F.; Roman, S.

2011-01-01

Activated carbons were prepared by different series of carbon dioxide and steam activation from walnut shells for their optimal use as radioactive methyl iodide adsorbents in Nuclear Plants. The knowledge of the most favourable textural characteristics of the activated carbons was possible by the previous study of the commercial activated carbon currently used for this purpose. In order to increase their methyl iodide affinity, the effect of triethylenediamine impregnation was studied at 5 and 10 wt.%. The results obtained indicated that in both cases the adsorption efficiency is markedly improved by the addition of impregnant, which allows the adsorbate uptake to occur not only by physical adsorption, via non-specific interactions (as in non-impregnated carbons) but also by the specific interaction of triethylenediamine with radioactive methyl iodide. Methyl iodide retention efficiencies up to 98.1% were achieved. (author)

Design concept for α-hydrogen-substituted nitroxides.

Science.gov (United States)

Amar, Michal; Bar, Sukanta; Iron, Mark A; Toledo, Hila; Tumanskii, Boris; Shimon, Linda J W; Botoshansky, Mark; Fridman, Natalia; Szpilman, Alex M

2015-02-06

Stable nitroxides (nitroxyl radicals) have many essential and unique applications in chemistry, biology and medicine. However, the factors influencing their stability are still under investigation, and this hinders the design and development of new nitroxides. Nitroxides with tertiary alkyl groups are generally stable but obviously highly encumbered. In contrast, α-hydrogen-substituted nitroxides are generally inherently unstable and rapidly decompose. Herein, a novel, concept for the design of stable cyclic α-hydrogen nitroxides is described, and a proof-of-concept in the form of the facile synthesis and characterization of two diverse series of stable α-hydrogen nitroxides is presented. The stability of these unique α-hydrogen nitroxides is attributed to a combination of steric and stereoelectronic effects by which disproportionation is kinetically precluded. These stabilizing effects are achieved by the use of a nitroxide co-planar substituent in the γ-position of the backbone of the nitroxide. This premise is supported by a computational study, which provides insight into the disproportionation pathways of α-hydrogen nitroxides.

Studies on hydrogen separation membrane for IS process. Membrane preparation with porous α-alumina tube

International Nuclear Information System (INIS)

Hwang, Gab-Jin; Onuki, Kaoru; Shimizu, Saburo

1998-01-01

It was investigated the preparation technique of hydrogen separation membrane to enhance the decomposition ratio of hydrogen iodide in the thermochemical IS process. Hydrogen separation membranes based on porous α-alumina tubes having pore size of 100 nm and 10 nm were prepared by chemical vapor deposition using tetraethylorthosilicate (TEOS) as the Si source. In the hydrogen separation membrane, its pore was closed by the deposited silica and then the permeation of gas was affected by the hindrance diffusion. At 600degC, the selectivity ratios (H 2 /N 2 ) were 5.2 and 160 for the membranes based on porous α-alumina tube having pore size of 100 nm and 10 nm, respectively. (author)

(2S,7S-10-Ethyl-1,8,10,12-tetraazatetracyclo[8.3.1.18,12.02,7]pentadecan-10-ium iodide

Directory of Open Access Journals (Sweden)

Augusto Rivera

2012-10-01

Full Text Available The title chiral quaternary ammonium salt, C13H25N4+·I−, was synthesized through the Menschutkin reaction between the cage aminal (2S,7S-1,8,10,12-tetraazatetracyclo[8.3.1.18,12.02,7]pentadecane and ethyl iodide. The quaternization occurred regioselectively on the nitrogen with major sp3 character. The crystal structure consists of anions and cations separated by normal distances. Ions are not linked through C—H...I hydrogen bonds.

Method of carbon dioxide-free hydrogen production from hydrocarbon decomposition over metal salts

Science.gov (United States)

Erlebacher, Jonah; Gaskey, Bernard

2017-10-03

A process to decompose methane into carbon (graphitic powder) and hydrogen (H.sub.2 gas) without secondary production of carbon dioxide, employing a cycle in which a secondary chemical is recycled and reused, is disclosed.

Adsorption of methyl iodide on charcoal

International Nuclear Information System (INIS)

Hidajat, K.; Aracil, J.; Kenney, C.N.

1990-01-01

The adsorption of non-radioactive methyl iodide has been measured experimentally over a range of conditions of concentration, and temperature on an activated charcoal. This is of interest since methyl iodide is formed from iodine fission products in gas cooled nuclear reactors. A mathematical model has also been developed which describes the rate of adsorption, under isothermal and linear adsorption isotherm conditions in a recycle adsorber. This model takes into account the resistance to adsorption caused by the surface adsorption, as well as the external and internal mass transfer resistances. The solution to the model for the recycle adsorber was obtained using a semidiscretisation method to reduce the partial differential equations to a system of stiff ordinary differential equations, and the resulting differential equations solved by a standard numerical technique. (author)

FY-2015 Methyl Iodide Deep-Bed Adsorption Test Report

International Nuclear Information System (INIS)

Soelberg, Nicholas Ray; Watson, Tony Leroy

2015-01-01

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 HNO 3 and increased NO 2 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 NO 2 , very low H 2 O 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 I 2 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.

Electrodeposition as an alternate method for preparation of environmental samples for iodide by AMS

Energy Technology Data Exchange (ETDEWEB)

Adamic, M.L., E-mail: Mary.Adamic@inl.gov [Idaho National Laboratory, P.O. Box 1625, Idaho Falls, ID 83402 (United States); Lister, T.E.; Dufek, E.J.; Jenson, D.D.; Olson, J.E. [Idaho National Laboratory, P.O. Box 1625, Idaho Falls, ID 83402 (United States); Vockenhuber, C. [Laboratory of Ion Beam Physics, ETH Zurich, Otto-Stern-Weg 5, 8093 Zurich (Switzerland); Watrous, M.G. [Idaho National Laboratory, P.O. Box 1625, Idaho Falls, ID 83402 (United States)

2015-10-15

This paper presents an evaluation of an alternate method for preparing environmental samples for {sup 129}I analysis by accelerator mass spectrometry (AMS) at Idaho National Laboratory. The optimal sample preparation method is characterized by ease of preparation, capability of processing very small quantities of iodide, and ease of loading into a cathode. Electrodeposition of iodide on a silver wire was evaluated using these criteria. This study indicates that the electrochemically-formed silver iodide deposits produce ion currents similar to those from precipitated silver iodide for the same sample mass. Precipitated silver iodide samples are usually mixed with niobium or silver powder prior to loading in a cathode. Using electrodeposition, the silver is already mixed with the sample and can simply be picked up with tweezers, placed in the sample die, and pressed into a cathode. The major advantage of this method is that the silver wire/electrodeposited silver iodide is much easier to load into a cathode.

Electrodeposition as an alternate method for preparation of environmental samples for iodide by AMS

International Nuclear Information System (INIS)

Adamic, M.L.; Lister, T.E.; Dufek, E.J.; Jenson, D.D.; Olson, J.E.; Vockenhuber, C.; Watrous, M.G.

2015-01-01

This paper presents an evaluation of an alternate method for preparing environmental samples for "1"2"9I analysis by accelerator mass spectrometry (AMS) at Idaho National Laboratory. The optimal sample preparation method is characterized by ease of preparation, capability of processing very small quantities of iodide, and ease of loading into a cathode. Electrodeposition of iodide on a silver wire was evaluated using these criteria. This study indicates that the electrochemically-formed silver iodide deposits produce ion currents similar to those from precipitated silver iodide for the same sample mass. Precipitated silver iodide samples are usually mixed with niobium or silver powder prior to loading in a cathode. Using electrodeposition, the silver is already mixed with the sample and can simply be picked up with tweezers, placed in the sample die, and pressed into a cathode. The major advantage of this method is that the silver wire/electrodeposited silver iodide is much easier to load into a cathode.

Autoradiolytic decomposition and reductant-free sodium sup 124 I- and sup 123 I-iodide

Energy Technology Data Exchange (ETDEWEB)

Sajjad, M.; Lambrecht, R.M.; Bakr, S.A. (King Faisal Specialist Hospital and Research Centre, Riyadh (Saudi Arabia). Radionuclide and Cyclotron Operations)

1990-01-01

The presence of salts and metal cations in {sup 124}I- and {sup 123}I-sodium iodide solutions separated from {sup 124}Te targets promots autoradiolytic decomposition of iodide to several different iodine species dependent upon the chemical environment. The stabilization of the radioiodine as iodide by removal of trace salts and trace metal cations and in the absence of reducing agents is described. The high specific activity {sup 123}I- and {sup 124}I-iodide is suitable for labeling antibodies, proteins and radiopharmaceuticals. (orig.).

An investigation of sodium iodide solubility in sodium-stainless steel systems

International Nuclear Information System (INIS)

Sagawa, Norihiko; Tashiro, Suguru

1996-01-01

Sodium iodide and major constituents of stainless steel in sodium are determined by using the steel capsules to obtain a better understanding on contribution of the constituents to the apparent iodide solubility in sodium. The capsule loaded with 20 g sodium and 0.1 - 0.3 g powder of sodium iodide is heated at its upper part in a furnace and cooled at its bottom on brass plates to establish a large temperature gradient along the capsule tube. After a given period of equilibration, the iodide and constituents are fixed in solidified sodium by quick quenching of the capsules. Sodium samples are taken from the sectioned capsule tube and submitted to sodium dissolution by vaporized water for determination of the iodine and to vacuum distillation for determination of the metal elements. Iron and nickel concentrations are observed to be lower in the samples at higher iodine concentrations. Chromium and manganese concentrations are seen to be insensitive to the iodine concentrations. The observations can be interpreted by a model that sodium oxide combines with metal iodide in sodium to form a complex compound and with consideration that the compound will fall and deposit onto the bottom of the capsule by thermal diffusion. (author)

R and D thermochemical I-S process at JAERI

International Nuclear Information System (INIS)

Onuki, K.; Kubo, S.; Nakajima, H.; Higashi, S.; Kasahara, S.; Ishiyama, S.; Okuda, H.

2004-01-01

The Japan Atomic Energy Research Institute (JAERI) has conducted a study on the thermochemical water-splitting process of the iodine-sulfur family (IS process). In the IS process, water will react with iodine and sulfur dioxide to produce hydrogen iodide and sulfuric acid, which are then decomposed thermally to produce hydrogen and oxygen. High temperature nuclear heat, mainly supplied by a High Temperature Gas-cooled Reactor (HTGR), is used to drive the endothermic decomposition of sulfuric acid. JAERI has demonstrated the feasibility of the water-splitting hydrogen production process by carrying out laboratory-scale experiments in which combined operation of fundamental reactions and separations using the IS process was performed continuously. At present, the hydrogen production test is continuing, using a scaled-up glass apparatus. Corrosion-resistant materials for constructing a large-scale plant and process improvements by introducing advanced separation techniques, such as membrane separation, are under study. Future R and D items are discussed based on the present activities. (author)

Responses of the soil decomposer community to the radioactive contamination

International Nuclear Information System (INIS)

Svetlana, Maksimova

2004-01-01

The knowledge about biodiversity and about reasons and laws of dynamics of decomposer invertebrates has exclusively important (rather applied, or theoretical) significance for soil science. Earthworms and millipedes are probably the most important members of the soil biota and major contributors to total zoo-mass. Their activities are such that they are extremely important in maintaining soil fertility in a variety of ways. They play an important part in the redistribution of radionuclides accumulated in the natural biogeocenoses and accumulation of radionuclides in their bodies depends on their concentration in the habitat. Since radionuclides can limit biological activity, studies to estimate the tolerance of decomposer community to potentially toxic radiators are needed. The effect of radioactive contamination on the soil invertebrates and decomposition processes in the different biogeocenoses we intensively studied during 17 years after Chernobyl accident. The soil invertebrates were collected according to generally accepted method by M. Ghilyarov. Soil samples were 0,25 m 2 and animals were extracted from samples by hand sorting. Usually decomposition was affected by the presence of decomposer fauna. Considerable differences were found in the species number. The species composition of sites differed clearly. The study showed that the fauna was poorer under increasing levels of radioactive contamination. The higher radionuclide content was found to result in suppression of decomposer community. The results showed a vertical migration of earthworms to deeper soil layers with increasing of radioactive contamination. With the absence of decomposer fauna due to migration to the deeper layer and mortality, the layer of litter increased. The results show that the earthworms were of small size. Cocoon production decreased. Radioactive contamination altered the process of reproduction and age structure of decomposer fauna. The invertebrates collected from the

Responses of the soil decomposer community to the radioactive contamination

Energy Technology Data Exchange (ETDEWEB)

Svetlana, Maksimova [Institute of Zoology of National Academy of Sciences of Belarus, Minsk (Belarus)

2004-07-01

The knowledge about biodiversity and about reasons and laws of dynamics of decomposer invertebrates has exclusively important (rather applied, or theoretical) significance for soil science. Earthworms and millipedes are probably the most important members of the soil biota and major contributors to total zoo-mass. Their activities are such that they are extremely important in maintaining soil fertility in a variety of ways. They play an important part in the redistribution of radionuclides accumulated in the natural biogeocenoses and accumulation of radionuclides in their bodies depends on their concentration in the habitat. Since radionuclides can limit biological activity, studies to estimate the tolerance of decomposer community to potentially toxic radiators are needed. The effect of radioactive contamination on the soil invertebrates and decomposition processes in the different biogeocenoses we intensively studied during 17 years after Chernobyl accident. The soil invertebrates were collected according to generally accepted method by M. Ghilyarov. Soil samples were 0,25 m{sup 2} and animals were extracted from samples by hand sorting. Usually decomposition was affected by the presence of decomposer fauna. Considerable differences were found in the species number. The species composition of sites differed clearly. The study showed that the fauna was poorer under increasing levels of radioactive contamination. The higher radionuclide content was found to result in suppression of decomposer community. The results showed a vertical migration of earthworms to deeper soil layers with increasing of radioactive contamination. With the absence of decomposer fauna due to migration to the deeper layer and mortality, the layer of litter increased. The results show that the earthworms were of small size. Cocoon production decreased. Radioactive contamination altered the process of reproduction and age structure of decomposer fauna. The invertebrates collected from the

Composing and decomposing data types

DEFF Research Database (Denmark)

Bahr, Patrick

2014-01-01

restrictive, disallowing subtypings that lead to more than one possible injection and should therefore be considered programming errors. Furthermore, from this refined subtyping constraint we derive a new constraint to express type isomorphism. We show how this isomorphism constraint allows us to decompose......Wouter Swierstra's data types à la carte is a technique to modularise data type definitions in Haskell. We give an alternative implementation of data types à la carte that offers more flexibility in composing and decomposing data types. To achieve this, we refine the subtyping constraint, which...... is at the centre of data types à la carte. On the one hand this refinement is more general, allowing subtypings that intuitively should hold but were not derivable beforehand. This aspect of our implementation removes previous restrictions on how data types can be combined. On the other hand our refinement is more...

Evaluation of quaternary ammonium halides for removal of methyl iodide from flowing air streams

International Nuclear Information System (INIS)

Freeman, W.P.; Mohacsi, T.G.; Kovach, J.L.

1985-01-01

The quaternary ammonium halides of several tertiary amines were used as impregnants on activated carbon and were tested for methyl iodide penetration in accordance with test Method A, ASTM D3803, 1979, ''Standard Test Methods for Radio-iodine Testing of Nuclear Grade Gas Phase Adsorbents''. The results suggest that the primary removal mechanism for methyl iodide-131 is isotopic exchange with the quaternary ammonium halide. For example, a 5 wt% impregnation of each of the tetramethyl, tetraethyl, tetrapropyl and tetrabutyl ammonium iodides on activated carbon yielded percent penetrations of 0.47, 0.53, 0.78, and 0.08 respectively when tested according to Method A of ASTM D3803. A sample impregnated with 5% tetramethyl ammonium hydroxide gave a methyl iodide penetration of 64.87%, thus supporting the isotopic exchange mechanism for removal. It has been a generally held belief that the success of tertiary amines as impregnants for radioiodine removal is a result of their ability to complex with the methyl iodide. The results of the work indicates that the superiority of the tertiary amines similar to triethylene diamine and quinuclidine, when compared to their straight chain analogs, is a result of their ease in reacting with methyl iodide-127 to form the quaternary ammonium iodide followed by isotopic exchange

Hydrogen production as a promising nuclear energy application

International Nuclear Information System (INIS)

Vanek, V.

2003-01-01

Hydrogen production from nuclear is a field of application which eventually can outweigh power production by nuclear power plants. There are two feasible routes of hydrogen production. The one uses heat to obtain hydrogen from natural gas through steam reforming of methane. This is an highly energy-consuming process requiring temperatures up to 900 deg C and producing carbon dioxide as a by-product. The other method includes direct thermochemical processes to obtain hydrogen, using sulfuric acid for instance. Sulfuric acid is decomposed thermally by the reaction: H 2 SO 4 -> H 2 O = SO 2 + (1/2) O 2 , followed by the processes I 2 + SO 2 + 2H O -> 2HI + H 2 SO 4 and 2HI -> H 2 + I 2 . The use of nuclear for this purpose is currently examined in Japan and in the US. (P.A.)

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.

Discovery of aryl-tri-fluoroborates as potent sodium/iodide sym-porter (NIS) inhibitors

International Nuclear Information System (INIS)

Lecat-Guillet, N.; Ambroise, Y.

2008-01-01

The structure-based design of sodium/iodide sym-porter (NIS) inhibitors identified new active compounds. The organo-tri-fluoroborate shown was found to inhibit iodide uptake with an IC50 value of 0.4 μM on rat-derived thyroid cells. The biological activity is rationalized by the presence of the BF3 - ion as a minimal binding motif for substrate recognition at the iodide binding site. (authors)

Discovery of aryl-tri-fluoroborates as potent sodium/iodide sym-porter (NIS) inhibitors

Energy Technology Data Exchange (ETDEWEB)

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

2008-07-01

The structure-based design of sodium/iodide sym-porter (NIS) inhibitors identified new active compounds. The organo-tri-fluoroborate shown was found to inhibit iodide uptake with an IC50 value of 0.4 {mu}M on rat-derived thyroid cells. The biological activity is rationalized by the presence of the BF3{sup -} ion as a minimal binding motif for substrate recognition at the iodide binding site. (authors)

Early effects of external gamma irradiation on iodide metabolism in rat thyroid

International Nuclear Information System (INIS)

Niatsetskaya, Z.; Nadolnik, L.

2006-01-01

Full text of publication follows: The exposure of the thyroid gland to therapeutic doses of external gamma irradiation is frequently associated with thyroid dysfunction. Although late irradiation effects are well documented, little is still known about the early functional alterations in the thyroid subjected to radiation therapy. The aim of this study was to examine the early effect of single external gamma irradiation on iodide metabolism in the thyroid. The Wistar female rats were irradiated using a 60 Co installation with a constant capacity of 0.64 Gy/min. The doses used were 0.25, 0.5, 1, 2, 5 Gy. The animals were sacrificed after 24 hours following the irradiation. T he thyroid organ culture was cultivated during 24 h and than was irradiated with a single dose of 5 Gy. The thyroid tissue was assayed for thyro-peroxidase activity and concentrations of total, free and protein -binding iodide. It was shown that the 0.25 Gy irradiation depressed thyroid iodide uptake, which was manifested in decreasing total iodide by 25%. The same tendency was observed after the 0.5 Gy irradiation. In the 1, 2, 5 Gy groups, the concentrations of total and free iodide increased by 26 -34% and 50-68%, accordingly. The level of protein-binding iodide in these groups was within the control values. However, protein-binding/total iodide and protein binding/ free iodide ratios decreased by 17 -41%, suggesting inhibition of thyroglobulin iodination. Thyro-peroxidase (T.P.O.) plays a key role in thyroid hormone synthesis by catalyzing both the iodination of thyroglobulin and the coupling some of the iodo-tyrosyl residues. After 24 hours on irradiation, a 31.5-54% dose-dependent inhibition of T.P.O. activity was shown in the 1, 2 and 5 Gy groups. The irradiation of the rat thyroid organ culture with a single dose of 5 Gy also led to significant inhibition of T.P.O. by 56.91% after 2 hours. We compared the enzyme kinetics of thyro-peroxidase from thyroid microsomal fraction control and

Process heat exchanger for SO3 decomposer fabricated with Ni-based alloys surface modified by SiC film deposition and N ion beam bombardment

International Nuclear Information System (INIS)

Park, Jae-Won; Kim, Hyung-Jin; Choi, Yong-Woon; Kim, Yong-Wan

2007-01-01

In the iodine-sulfur (IS) cycle for the hydrogen production using the high temperature gas-cooled reactor (HTGR), one of the important components is the SO 3 decomposer which generates SO 2 and SO 3 gases under high temperature conditions. Since this environment is extremely corrosive, the materials used for the decomposer should meet excellent mechanical properties at the elevated temperature as well as high corrosion resistance in SO 2 /SO 3 atmospheres. In general, ceramics are protective against the corrosion, but metals exhibit limited corrosion resistance. In this work, the ceramic coating on the metallic substrate was studied. We selected SiC as coating materials and Ni-based alloys as the substrate materials. Since the adhesion between the coated layer and the substrate is most crucial in this application, we attempted to develop Ion Beam Mixing (IBM) technique to produce a highly adherent coated layer. For the fabrication of process heat exchange for SO 3 decomposer, the diffusion bonding at ∼900 .deg. C is employed because this temperature does not affect the mechanical properties of materials

Linearity and Reversibility of Iodide Adsorption on Sediments from Hanford, Washington Under Water Saturated Conditions

International Nuclear Information System (INIS)

Um, Wooyong; Serne, R. Jeffrey; Krupka, Kenneth M.

2004-01-01

A series of adsorption and desorption experiments were completed to determine the linearity of iodide adsorption, as a function of concentration, and its reversibility onto sediment for geochemical conditions germane to the proposed disposal of low-level radioactive waste by the U.S. Department of Energy's Immobilized Low Activity Waste (ILAW) program at the Hanford Site in southeastern Washington. Iodine-129 is predicted to be one of the top three long-term risk drivers based on past performance assessment conducted for the eventual disposal of the low-level portion of radioactive wastes currently stored in underground storage tanks at Hanford, because iodide exhibits little adsorption affinity to mineral surfaces resulting in high mobility in the subsurface environment. Adsorption experiments, conducted with Hanford formation sediments and groundwater spiked with dissolved 125I (as an analog tracer for 129I), indicated that iodide adsorption was very low at pH 7.5 and could be represented by a linear isotherm up to a total concentration of 100 mg/L dissolved iodide. The linearity of iodide adsorption up to concentrations of 100 mg/L validates the use of the linear Kd construct in transport models to predict the fate and transport of 129I in subsurface systems at Hanford. The results of desorption experiments indicated that up to 60% of adsorbed iodide was readily desorbed after 14 days by the same groundwater solution. Iodide adsorption was considered to be partially reversible or weakly binding on the sediments. Even though small amount of initial iodide is retarded by adsorption reactions at mineral-water interfaces, the weak adsorption affinity results in release of iodide when iodide free pore waters and ground waters contact the contaminated sediments in the vadose zone and aquifer systems

Sodium iodide symporter: Its role in nuclear oncology

International Nuclear Information System (INIS)

Chung, June-Key

2004-01-01

Full text: Thyroid iodide uptake is basic to the clinical applications of radioiodine in diagnosis and therapy. Iodide uptake occurs across the membrane of thyroid follicular cells via an active transporter process mediated by the sodium/iodide symporter (NIS). The recent cloning of the gene encoding NIS enabled better characterization of the molecular mechanisms underlying the iodide transport, thus opening the way to clarify and expand its role in medicine. NIS contains 13 transmembrane segments, and its gene encodes a glycoprotein of 643 amino acids. Decreased NIS expression levels account for the reduced iodide uptake in thyroid carcinomas. We found that thyroid cancer patients with positive immunostaining for NIS responded to I-131 therapy better than did the patients with negative immunostaining. Thus, NIS gene can be used for radionuclide gene therapy. Targeted expression of functional NIS in cancer cells would enable these cells to concentrate iodide from plasma and would, therefore, offer the possibility of radioiodine therapy. We and others have shown that gene transfer of NIS into a variety of cell types confers increased radioiodine uptake up to several hundred-fold that of controls. There is great interest in exploring the possibility of NIS gene transfer to facilitate radioiodine therapy for non-thyroidal human cancers including hepatoma, prostate, breast, colon cancers as well as thyroid cancer. Recently, several approaches such as, targeted gene transfer, thyroid peroxidase gene co-transfection, retinoic acid treatment and Re-188 therapy instead of I-131, have been tried to improve this novel gene therapy. Imaging reporter gene is useful in non-invasively determining the location, duration and magnitude of transgene expression in living animal. Conventionally, HSV-tk and dopaminergic receptor (D2R) genes have been presented as possible imaging reporter genes. We proved that NIS could serve as an alternative imaging reporter gene. NIS has many

Liquid composition having ammonia borane and decomposing to form hydrogen and liquid reaction product

Science.gov (United States)

Davis, Benjamin L; Rekken, Brian D

2014-04-01

Liquid compositions of ammonia borane and a suitably chosen amine borane material were prepared and subjected to conditions suitable for their thermal decomposition in a closed system that resulted in hydrogen and a liquid reaction product.

Iodine K-edge EXAFS analysis of iodide ion-cyclodextrin inclusion complexes in aqueous solution

International Nuclear Information System (INIS)

Kaneko, T; Ueda, M; Nagamatsu, S; Konishi, T; Fujikawa, T; Mizumaki, M

2009-01-01

We study the structure of inclusion complexes of α-, β-, γ-cyclodextrin with mono-iodide ion in aqueous solution by means of iodine K-edge EXAFS spectroscopy. The analysis is based on the assumption that two kinds of iodide ions exist in KI-cyclodextrin aqueous solution i.e. hydrated mono-iodide ions and one-one mono-iodide-cyclodextrin inclusion complexes. In KI-α-cyclodextrin system, iodine K-edge EXAFS analyse show that the average coordination number of the oxygen atoms in water molecules in the first hydration shell decreases as the fraction of included ions increases. This result suggests that dehydration process accompanies the formation of the inclusion complex. This is not found in the case of β-cyclodextrin, indicating that in this case the iodide ions are included together with the whole first hydration shell.

Clinical value of sodium iodide symporter

International Nuclear Information System (INIS)

Li Qian

2003-01-01

The sodium iodide symptorter (NIS) is a membrane glycoprotein that mediates iodide uptake in the thyroid gland and several extrathyroidal tissues. In addition to thyroid tissues, the expression of NIS is found in stomach, prostate, placenta and so on. Radioiodine-concentrating activity in thyroid tissues has allowed the use of radioiodine as a diagnostic and therapeutic agent for patients with thyroid disorders. However, some extrathyroid tissues also take up radioiodine, contributing to unwanted side effects of radioiodine therapy. Now that the molecule of NIS has been cloned and characterized, it may be possible to develop novel strategies to differentially modulate NIS expression and activity, enhancing it in target tissues and impeding it in others. It is also important to explore the use of NIS as an imaging reporter gene to monitor the expression profile of the transgene in transgenic mouse animal models and in patients undergoing gene therapy clinical trials

Integrated boiler, superheater, and decomposer for sulfuric acid decomposition

Science.gov (United States)

Moore, Robert [Edgewood, NM; Pickard, Paul S [Albuquerque, NM; Parma, Jr., Edward J.; Vernon, Milton E [Albuquerque, NM; Gelbard, Fred [Albuquerque, NM; Lenard, Roger X [Edgewood, NM

2010-01-12

A method and apparatus, constructed of ceramics and other corrosion resistant materials, for decomposing sulfuric acid into sulfur dioxide, oxygen and water using an integrated boiler, superheater, and decomposer unit comprising a bayonet-type, dual-tube, counter-flow heat exchanger with a catalytic insert and a central baffle to increase recuperation efficiency.

Procedures for Decomposing a Redox Reaction into Half-Reaction

Science.gov (United States)

Fishtik, Ilie; Berka, Ladislav H.

2005-01-01

A simple algorithm for a complete enumeration of the possible ways a redox reaction (RR) might be uniquely decomposed into half-reactions (HRs) using the response reactions (RERs) formalism is presented. A complete enumeration of the possible ways a RR may be decomposed into HRs is equivalent to a complete enumeration of stoichiometrically…

Process simulation of nuclear-based thermochemical hydrogen production with a copper-chlorine cycle

International Nuclear Information System (INIS)

Chukwu, C.C.; Naterer, G.F.; Rosen, M.A.

2008-01-01

Thermochemical processes for hydrogen production driven by nuclear energy are promising alternatives to existing technologies for large-scale commercial production of hydrogen without fossil fuels. The copper-chlorine (Cu-Cl) cycle, in which water is decomposed into hydrogen and oxygen, is promising for thermochemical hydrogen production in conjunction with a Supercritical Water Cooled Reactor. Here, the cycle efficiency is examined using the Aspen Plus process simulation code. Possible efficiency improvements are discussed. The results are expected to assist the development of a lab-scale cycle demonstration, which is currently being undertaken at University of Ontario Institute of Technology in collaboration with numerous partners. (author)

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.

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

International Nuclear Information System (INIS)

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

1988-01-01

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 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 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

8a-Methyl-5,6,8,8a,9,10-hexahydro-10,12a-epoxyisoindolo[1,2-a]isoquinolinium iodide

Directory of Open Access Journals (Sweden)

Flavien A. A. Toze

2010-06-01

Full Text Available The title compound, C17H18NO+·I−, is an adduct resulting from an intramolecular Diels–Alder reaction of methallyl chloride with 3,4-dihydro-1-furylisoquinoline. The cation comprises a fused pentacyclic system containing three five-membered rings (dihydropyrrole, dihydrofuran and tetrahydrofuran and two six-membered rings (tetrahydropyridine and benzene. The five-membered rings have the usual envelope conformations, and the central six-membered tetrahydropyridine ring adopts the unsymmetrical half-boat conformation. In the crystal, cations and iodide anions are bound by weak intermolecular hydrogen-bonding interactions into a three-dimensional framework.

The value of iodide as a parameter in the chemical characterisation of groundwaters

Science.gov (United States)

Lloyd, J. W.; Howard, K. W. F.; Pacey, N. R.; Tellam, J. H.

1982-06-01

Brackish and saline groundwaters can severely constrain the use of fresh groundwaters. Their chemical characterisation is important in understanding the hydraulic conditions controlling their presence in an aquifer. Major ions are frequently of limited value but minor ions can be used. Iodide in groundwater is particularly significant in many environments due to the presence of soluble iodine in aquifer matrix materials. Iodide is found in groundwaters in parts of the English Chalk aquifer in concentrations higher than are present in modern seawater. Its presence is considered as a indication of groundwater residence and is of use in the characterisation of fresh as well as saline waters. Under certain circumstances modern seawater intrusion into aquifers along English estuaries produces groundwaters which are easily identified due to iodide enrichment from estuarine muds. In other environments iodide concentrations are of value in distinguishing between groundwaters in limestones and shaly gypsiferous rocks as shown by a study in Qatar, while in an alluvial aquifer study in Peru iodide has been used to identify groundwaters entering the aquifer from adjacent granodiorites.

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

International Nuclear Information System (INIS)

Hermon, H.; James, R.B.; Lund, J.

1998-01-01

In this study the authors report on the results of the investigation of lead iodide material properties. The effectiveness of a zone refining purification method on the material purity is determined by ICP-MS and ICP-OES and correlated to the electrical and physical material properties. They show that this zone refining method is very efficient in removing impurities from lead iodide, and they 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 much 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

Structural templating in a nonplanar phthalocyanine using single crystal copper iodide

OpenAIRE

Rochford, L. A. (Luke A.); Ramadan, Alexandra J.; Keeble, Dean S.; Ryan, Mary P.; Heutz, Sandrine; Jones, T. S. (Tim S.)

2015-01-01

Solution-grown copper iodide crystals are used as substrates for the templated growth of the nonplanar vanadyl phthalocyanine using organic molecular beam deposition. Structural characterization reveals a single molecular orientation produced by the (111) Miller plane of the copper iodide crystals. These fundamental measurements show the importance of morphology and structure in templating interactions for organic electronics applications.

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

Gravimetric determination of cadmium with o-phenanthroline and iodide

International Nuclear Information System (INIS)

Yoshida, Hitoshi; Mizuno, Kazunori; Taga, Mitsuhiko; Hikime, Seiichiro

1976-01-01

Cadmium forms insoluble mixed ligand complex with o-phenanthroline and iodide ions. By using the complex a new gravimetric method for the determination of cadmium was investigated. The recommended analytical procedure is as follows: Adjust pH value of a solution containing 5 to 45 mg cadmium to 4 with 3 M acetic acid-sodium acetate buffer solution. Add over threefold moles of potassium iodide to the solution and heat to just before boiling. To the solution add 0.1% ascorbic acid solution and then 0.1 M o-phenanthroline solution drop by drop in excess with stirring, and cool the mixture to room temperature. Filter the precipitates and wash first with 0.01% potassium iodide solution and then with water. Dry the precipitates at 110 0 C for two hours and weigh as Cd(o-phen) 2 I 2 (I). The gravimetric factor of the complex for cadmium is 0.1547. Chemical composition of the precipitate is variable when o-phenanthroline is added less than twofold moles to cadmium. Adding the o-phenanthroline solution 2.4-fold moles against cadmium, the ternary complex (I) precipitates quantitatively. Though a large excess of iodide ion in the solution contaminated the precipitate, the contamination was avoided when precipitation was carryed out at high temperature and in the presence of ascorbic acid. By the presented procedure 5 to 45 mg of cadmium are determined with a standard deviation of 0 C. (JPN)

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.

Functional activity of human sodium/iodide symporter in tumor cell lines

International Nuclear Information System (INIS)

Petrich, T.; Knapp, W.H.; Poetter, E.

2003-01-01

Aim: The sodium/iodide symporter (NIS) actively transports iodide into thyrocytes. Thus, NIS represents a key protein for diagnosis and radioiodine therapy of differentiated thyroid cancer. Additionally, in the future the NIS gene may be used for cancer gene therapy of non-thyroid-derived malignancies. In this study we evaluated the functionality of NIS with respect to iodide uptake in a panel of tumor cell lines and compared this to gene transfer efficiency. Methods: A human NIS-containing expression vector and reporter-gene vectors encoding and beta;-Galactosidase- or EGFP were used for transient transfection of 13 tumor cell lines. Following transfection measurements of NIS-mediated radioiodide uptake using Na 125 I and of transfection efficiency were performed. The latter included β;-Galactosidase activity measurements using a commercial kit and observation by fluorescence microscopy for EGFP expression. Results: In contrast to respective parental cells, most NIS-transfected cell lines displayed high, perchlorate-sensitive radioiodide uptake. Differences in radioiodide uptake between cell lines apparently corresponded to transfection efficiencies, as judged from reporter-gene assays. Conclusion: With respect to iodide uptake we provide evidence that NIS is functional in different cellular context. As iodide uptake capacity appears to be well correlated to gene transfer efficiency, cell type-specific actions on NIS (e. g. post-translational modification such as glycosylation) are not inhibitory to NIS function. Our data support the promising role of NIS in cancer gene therapy strategies. (orig.)

Role of sodium hydroxide in the production of hydrogen gas from the hydrothermal gasification of biomass

Energy Technology Data Exchange (ETDEWEB)

Onwudili, Jude A.; Williams, Paul T. [Energy and Resources Research Institute, University of Leeds, Leeds, LS2 9JT (United Kingdom)

2009-07-15

The role of sodium hydroxide as a promoter of hydrogen gas production during the hydrothermal gasification of glucose and other biomass samples has been investigated. Experiments were carried out in a batch reactor with glucose and also in the presence of the alkali from 200 C, 2 MPa to 450 C, 34 MPa at constant water loading. Without sodium hydroxide, glucose decomposed to produce mainly carbon dioxide, water, char and tar. Furfural, its derivatives and reaction products dominated the ethyl acetate extract of the water (organic fraction) at lower reaction conditions. This indicated that the dehydration of glucose to yield these products was unfavourable to hydrogen gas production. In the presence of sodium hydroxide however, glucose initially decomposed to form mostly alkylated and hydroxylated carbonyl compounds, whose further decomposition yielded hydrogen gas. It was observed that at 350 C, 21.5 MPa, half of the optimum hydrogen gas yield had formed and at 450 C, 34 MPa, more than 80 volume percent of the gaseous effluent was hydrogen gas, while the balance was hydrocarbon gases, mostly methane ({>=}10 volume percent). Other biomass samples were also comparably reacted at the optimum conditions observed for glucose. The rate of hydrogen production for the biomass samples was in the following order; glucose > cellulose, starch, rice straw > potato > rice husk. (author)

Experimental studies of caesium iodide aerosol condensation: theoretical interpretation

International Nuclear Information System (INIS)

Beard, A.M.; Benson, C.G.; Horton, K.D.; Buckle, E.R.

1990-07-01

Caesium iodide is predicted to be a significant source of fission product aerosols during the course of a severe accident in a pressurised water reactor (PWR). The nucleation and growth of caesium iodide aerosols have been studied using a plume chamber and the results compared with theoretical values calculated using the approach developed by Buckle for aerosol nucleation. The morphology of the particles was studied using scanning electron microscopy (SEM) and transmission optical microscopy (TOM), whilst the particle size distributions were determined from differential mobility (DMPS) and aerodynamic (APS) measurements. (author)

Hydrogen

Directory of Open Access Journals (Sweden)

John O’M. Bockris

2011-11-01

Full Text Available The idea of a “Hydrogen Economy” is that carbon containing fuels should be replaced by hydrogen, thus eliminating air pollution and growth of CO2 in the atmosphere. However, storage of a gas, its transport and reconversion to electricity doubles the cost of H2 from the electrolyzer. Methanol made with CO2 from the atmosphere is a zero carbon fuel created from inexhaustible components from the atmosphere. Extensive work on the splitting of water by bacteria shows that if wastes are used as the origin of feed for certain bacteria, the cost for hydrogen becomes lower than any yet known. The first creation of hydrogen and electricity from light was carried out in 1976 by Ohashi et al. at Flinders University in Australia. Improvements in knowledge of the structure of the semiconductor-solution system used in a solar breakdown of water has led to the discovery of surface states which take part in giving rise to hydrogen (Khan. Photoelectrocatalysis made a ten times increase in the efficiency of the photo production of hydrogen from water. The use of two electrode cells; p and n semiconductors respectively, was first introduced by Uosaki in 1978. Most photoanodes decompose during the photoelectrolysis. To avoid this, it has been necessary to create a transparent shield between the semiconductor and its electronic properties and the solution. In this way, 8.5% at 25 °C and 9.5% at 50 °C has been reached in the photo dissociation of water (GaP and InAs by Kainthla and Barbara Zeleney in 1989. A large consortium has been funded by the US government at the California Institute of Technology under the direction of Nathan Lewis. The decomposition of water by light is the main aim of this group. Whether light will be the origin of the post fossil fuel supply of energy may be questionable, but the maximum program in this direction is likely to come from Cal. Tech.

Hydrogen.

Science.gov (United States)

Bockris, John O'M

2011-11-30

The idea of a "Hydrogen Economy" is that carbon containing fuels should be replaced by hydrogen, thus eliminating air pollution and growth of CO₂ in the atmosphere. However, storage of a gas, its transport and reconversion to electricity doubles the cost of H₂ from the electrolyzer. Methanol made with CO₂ from the atmosphere is a zero carbon fuel created from inexhaustible components from the atmosphere. Extensive work on the splitting of water by bacteria shows that if wastes are used as the origin of feed for certain bacteria, the cost for hydrogen becomes lower than any yet known. The first creation of hydrogen and electricity from light was carried out in 1976 by Ohashi et al. at Flinders University in Australia. Improvements in knowledge of the structure of the semiconductor-solution system used in a solar breakdown of water has led to the discovery of surface states which take part in giving rise to hydrogen (Khan). Photoelectrocatalysis made a ten times increase in the efficiency of the photo production of hydrogen from water. The use of two electrode cells; p and n semiconductors respectively, was first introduced by Uosaki in 1978. Most photoanodes decompose during the photoelectrolysis. To avoid this, it has been necessary to create a transparent shield between the semiconductor and its electronic properties and the solution. In this way, 8.5% at 25 °C and 9.5% at 50 °C has been reached in the photo dissociation of water (GaP and InAs) by Kainthla and Barbara Zeleney in 1989. A large consortium has been funded by the US government at the California Institute of Technology under the direction of Nathan Lewis. The decomposition of water by light is the main aim of this group. Whether light will be the origin of the post fossil fuel supply of energy may be questionable, but the maximum program in this direction is likely to come from Cal. Tech.

Radiolysis of cesium iodide solutions in conditions prevailing in a pressurized water reactor severe accident

International Nuclear Information System (INIS)

Lucas, M.

1988-01-01

Measurements were made of I/sub 2/ formed when aqueous cesium iodide (CsI) solutions were exposed to two temperatures, 43 and 95 0 C, with irradiation. Iodine partition coefficients were obtained from the experiments. The parameters varied were dose, CsI concentration, and Cs/sub 2/CO/sub 3/ concentration, in the presence of air-carbon dioxide and air-carbon dioxide-hydrogen mixtures, to provide information to calculate the form in which iodine released from fuel as CsI in a reactor accident might reach the environment. In a series of experiments, a two-compartment cell was used to trap the gaseous iodine produced. In this case, it was found that the quantity of gaseous iodine produced increased approximately linearly with the dose (at the dose rate used)

Monitoring of fluoride and iodide levels in drinking water using ion selective electrodes

International Nuclear Information System (INIS)

Ahmed, R.; Viqar-Un-Nisa; Hussain, M.; Tanwir, R.; Qureshi, S.A.

2004-01-01

Fluoride and iodide, the most important constituents of drinking water are essential as well as toxic depending on their levels. For their analysis in water mostly ion-selective electrodes, spectrophotometry, titrimetry and coulometry etc; have been used and literature has been briefly reviewed. Ion-selective electrodes offer an efficient method for the measurement of the two halides and were mostly used during this work. Fabrication of these electrodes is briefly described. Comparison of results obtained by ion selective electrode and coulometry is given. Recoveries of the added fluoride ions from the samples were good. A large number of water samples from Rawalpindi-Islamabad area were analyzed for fluoride and iodide. Levels of fluoride and iodide from two main water reservoirs of Rawalpindi and Islamabad are reported before and after treatment. Both surface and ground water samples were analyzed and results are compared and discussed. Some samples from northern areas were also analyzed for iodide and fluoride and compared. Intake of fluoride and iodide from water of different areas is also compared. Water samples, which caused bone deformation in certain areas in Punjab due to excess fluoride, were also analyzed for fluoride and results are presented. (author)

Stable iodide doping induced by photonic curing for carbon nanotube transparent conductive films

Science.gov (United States)

Wachi, Atsushi; Nishikawa, Hiroyuki; Zhou, Ying; Azumi, Reiko

2018-06-01

Doping has become crucial for achieving stable and high-performance conductive transparent carbon nanotube (CNT) films. In this study, we systematically investigate the doping effects of a few materials including alkali metal iodides, nonmetal iodide, and metals. We demonstrate that photonic curing can enhance the doping effects, and correspondingly improve the conductivity of CNT films, and that such iodides have better doping effects than metals. In particular, doping with a nonmetal compound (NH4I) shows the largest potential to improve the conductivity of CNT films. Typically, doping with metal iodides reduces the sheet resistance (R S) of CNT films with 70–80% optical transmittances at λ = 550 nm from 600–2400 to 250–440 Ω/square, whereas doping with NH4I reduces R S to 57 and 84 Ω/square at 74 and 84% optical transmittances, respectively. Interestingly, such a doped CNT film exhibits only a slight increase in sheet resistance under an extreme environment of high temperature (85 °C) and high relative humidity (85%) for 350 h. The results suggest that photonic-curing-induced iodide doping is a promising approach to producing high-performance conductive transparent CNT films.

Vapor pressure of selected organic iodides

Czech Academy of Sciences Publication Activity Database

Fulem, M.; Růžička, K.; Morávek, P.; Pangrác, Jiří; Hulicius, Eduard; Kozyrkin, B.; Shatunov, V.

2010-01-01

Roč. 55, č. 11 (2010), 4780-4784 ISSN 0021-9568 R&D Projects: GA ČR GA203/08/0217 Institutional research plan: CEZ:AV0Z10100521 Keywords : vapor pressure * static method * organic iodides Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 2.089, year : 2010

Traits determining the digestibility-decomposability relationships in species from Mediterranean rangelands.

Science.gov (United States)

Bumb, Iris; Garnier, Eric; Coq, Sylvain; Nahmani, Johanne; Del Rey Granado, Maria; Gimenez, Olivier; Kazakou, Elena

2018-03-05

Forage quality for herbivores and litter quality for decomposers are two key plant properties affecting ecosystem carbon and nutrient cycling. Although there is a positive relationship between palatability and decomposition, very few studies have focused on larger vertebrate herbivores while considering links between the digestibility of living leaves and stems and the decomposability of litter and associated traits. The hypothesis tested is that some defences of living organs would reduce their digestibility and, as a consequence, their litter decomposability, through 'afterlife' effects. Additionally in high-fertility conditions the presence of intense herbivory would select for communities dominated by fast-growing plants, which are able to compensate for tissue loss by herbivory, producing both highly digestible organs and easily decomposable litter. Relationships between dry matter digestibility and decomposability were quantified in 16 dominant species from Mediterranean rangelands, which are subject to management regimes that differ in grazing intensity and fertilization. The digestibility and decomposability of leaves and stems were estimated at peak standing biomass, in plots that were either fertilized and intensively grazed or unfertilized and moderately grazed. Several traits were measured on living and senesced organs: fibre content, dry matter content and nitrogen, phosphorus and tannin concentrations. Digestibility was positively related to decomposability, both properties being influenced in the same direction by management regime, organ and growth forms. Digestibility of leaves and stems was negatively related to their fibre concentrations, and positively related to their nitrogen concentration. Decomposability was more strongly related to traits measured on living organs than on litter. Digestibility and decomposition were governed by similar structural traits, in particular fibre concentration, affecting both herbivores and micro

Decomposing change in life expectancy

DEFF Research Database (Denmark)

Vaupel, James W.; Canudas Romo, Vladimir

2003-01-01

We extend Nathan Keyfitz's research on continuous change in life expectancy over time by presenting and proving a new formula for decomposing such change. The formula separates change in life expectancy over time into two terms. The first term captures the general effect of reduction in death rates...... in Sweden and Japan....

Studies on membrane acid electrolysis for hydrogen production

Energy Technology Data Exchange (ETDEWEB)

Silva, Marco Antonio Oliveira da; Linardi, Marcelo; Saliba-Silva, Adonis Marcelo [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil). Centro de Celulas a Combustivel e Hidrogenio], Email: saliba@ipen.br

2010-07-01

Hydrogen represents great opportunity to be a substitute for fossil fuels in the future. Water as a renewable source of hydrogen is of great interest, since it is abundant and can decompose, producing only pure H{sub 2} and O{sub 2}. This decomposition of water can be accomplished by processes such as electrolysis, thermal decomposition and thermochemical cycles. The electrolysis by membrane has been proposed as a viable process for hydrogen production using thermal and electrical energy derived from nuclear energy or any renewable source like solar energy. In this work, within the context of optimization of the electrolysis process, it is intended to develop a mathematical model that can simulate and assist in parameterization of the electrolysis performed by polymer membrane electrolytic cell. The experimental process to produce hydrogen via the cell membrane, aims to optimize the amount of gas produced using renewable energy with noncarbogenic causing no harm by producing gases deleterious to the environment. (author)

21 CFR 184.1265 - Cuprous iodide.

Science.gov (United States)

2010-04-01

... the following specific limitations: Category of food Maximum treatment level in food Functional use... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Cuprous iodide. 184.1265 Section 184.1265 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN...

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.

Determination of peracetic acid and hydrogen peroxide in the mixture

OpenAIRE

Bodiroga Milanka; Ognjanović Jasminka

2002-01-01

Iodometric and permanganometric titrations were used for determination of peracetic acid and hydrogen peroxide (H2O2) in the mixture. Two procedures were described and compared. Titrations could be done in only one vessel, in the same reaction mixture, when iodometric titration of peracetic acid was continued after the permanganometric titration of H2O2, (procedure A). Peracetic acid and H2O2, as oxidizing agents, reacted with potassium iodide in an acid medium, evolving iodine. This reaction...

Potentiometric sensing of iodide using polymeric membranes of microwave stabilized β-AgI

International Nuclear Information System (INIS)

James, Dhanya; Rao, T. Prasada

2012-01-01

Highlights: ► Stable β-phase was obtained by post MW irradiation of AgI precipitate. ► Constructed ISEby dispersing stable β-AgI crystals in polyvinyl chloride. ► Designed iodide ISE exhibited wide linear range and fast response. ► Highly selective with selectivity factors less than 10 −6 . ► Successfully applied to natural waters, table salt and human urine samples. - Abstract: A polymer based heterogeneous ion selective electrode (ISE) membrane was fabricated for the potentiometric sensing of iodide. The sensing element used for the preparation of the ISE membrane was microwave stabilized β-AgI. Because microwave energy was found to be beneficial for causing hysteresis at the phase transition temperature of AgI, an attempt has been made to prepare stable and conductive β-AgI crystals by post microwave irradiation under high pressure. A conventionally precipitated AgI based ISE was also fabricated for comparative studies. The β-AgI based ISE could respond to a wide range of iodide concentrations (1 × 10 −8 to 1 M) within 60 s with a detection limit of 10 nM. The ISE gave stable response to iodide ions in a pH range of 2.0–8.0 and was highly selective in the presence of various interfering ions. The performance of the proposed iodide ISE in the analysis of natural and seawater samples was encouraging, and the determination of iodide in table salt and human urine samples was explained using the developed sensor.

Potentiometric determination of iodides in urine

International Nuclear Information System (INIS)

Gikolaev, B.A.; Primakova, L.N.; Rakhman'ko, E.M.

1996-01-01

Variants of potentiometric method: determination using a calibrations plot, the Gran method, and the double addition method are considered. The method of double additions of the test solution to the reference one is suggested as the most favorable method of determining iodides in urine under clinical laboratory conditions. Refs. 5, tabs. 2

Inclusion complexation of tetrabutylammonium iodide by cyclodextrins

Indian Academy of Sciences (India)

Biswajit Datta

Host-guest inclusion complex of an ionic solid (tetrabutyl ammonium iodide) with α- and β- cyclodextrin has been ... tions.2 CDs are cyclic oligomer of α-D-glucose having numerous of ... of locating at the interface of two phases (liquid–liquid.

Iodide behaviour in hard clay rocks under controlled physico-chemical conditions at different concentrations

International Nuclear Information System (INIS)

Frasca, B.; Savoye, S.; Wittebroodt, C.; Leupin, O.X.; Descostes, M.; Grenut, B.; Meier, P.; Michelot, J.L.

2010-01-01

Document available in extended abstract form only. With a half-life of 1.6 10 7 years, its high mobility and its potential to accumulate in the biosphere, iodine-129 is considered, from safety assessment calculations for radioactive waste repositories, to be one of the main radiological dose contributors. Based on the findings of previous studies, iodide, especially at low concentrations, seems to be migrating at a slower rate in clay rock than Cl-36. The cause of this retardation regarding the diffusion of iodide versus chloride is not yet understood but several hypotheses are point towards sorption on natural organic matter (NOM), pyrite or redox reactions. Oxidation of iodide would form IO 3 - which is known to have a higher sorption affinity on several soils and sediment samples than iodide. The present project aims at exploring the effect on the iodide behaviour of two parameters: (i) the initial concentration of iodide and (ii) the amount of NOM contained in the argillite samples. Such an investigation is carried out on Tournemire argillite by means of both batch and through-diffusion experiments. The main challenge is to exclude as much as possible the occurrence of any experimental artefact that could induce iodide uptake (oxygen contamination, dissolution/precipitation of carbonate phases). Regarding redox conditions and rock equilibrium, all the experiments were carried out under physico-chemical conditions as close as possible to those prevailing in field. Using a glove box with an atmosphere of N 2 /CO 2 (respectively 99.6% and 0.4%), we preserved the experiments from oxygen and maintained the calculated in-situ carbonate equilibrium. At first, four through-diffusion experiments with the non-sorbing tracers HTO and Cl-36 were performed to allow the diffusive parameters of each sample to be defined. Afterwards, iodide was injected in the diffusion cells at four different concentrations (10 -6 M to 10 -3 M). Thus, the comparison of the incoming fluxes of

Thermochemical hydrogen production based on magnetic fusion

International Nuclear Information System (INIS)

Krikorian, O.H.; Brown, L.C.

1982-01-01

Conceptual design studies have been carried out on an integrated fusion/chemical plant system using a Tandem Mirror Reactor fusion energy source to drive the General Atomic Sulfur-Iodine Water-Splitting Cycle and produce hydrogen as a future feedstock for synthetic fuels. Blanket design studies for the Tandem Mirror Reactor show that several design alternatives are available for providing heat at sufficiently high temperatures to drive the General Atomic Cycle. The concept of a Joule-boosted decomposer is introduced in one of the systems investigated to provide heat electrically for the highest temperature step in the cycle (the SO 3 decomposition step), and thus lower blanket design requirements and costs. Flowsheeting and conceptual process designs have been developed for a complete fusion-driven hydrogen plant, and the information has been used to develop a plot plan for the plant and to estimate hydrogen production costs. Both public and private utility financing approaches have been used to obtain hydrogen production costs of $12-14/GJ based on July 1980 dollars

Evaluation of optimal silver amount for the removal of methyl iodide on silver-impregnated adsorbents

International Nuclear Information System (INIS)

Park, G.I.; Cho, I.H.; Kim, J.H.; Oh, W.Z.

2001-01-01

The adsorption characteristics of methyl iodide generated from the simulated off-gas stream on various adsorbents such as silver-impregnated zeolite (AgX), zeocarbon and activated carbon were investigated. An extensive evaluation was made on the optimal silver impregnation amount for the removal of methyl iodide at temperatures up to 300 deg. C. The degree of adsorption efficiency of methyl iodide on silver-impregnated adsorbent is strongly dependent on impregnation amount and process temperature. A quantitative comparison of adsorption efficiencies on three adsorbents in a fixed bed was investigated. The influence of temperature, methyl iodide concentration and silver impregnation amount on the adsorption efficiency is closely related to the pore characteristics of adsorbents. It shows that the effective impregnation ratio was about 10wt%, based on the degree of silver utilization for the removal of methyl iodide. The practical applicability of silver-impregnated zeolite for the removal of radioiodine generated from the DUPIC process was consequently proposed. (author)

Determination of iodide, iodate and organo-iodine in waters with a new total organic iodine measurement approach.

Science.gov (United States)

Gong, Tingting; Zhang, Xiangru

2013-11-01

The dissolved iodine species that dominate aquatic systems are iodide, iodate and organo-iodine. These species may undergo transformation to one another and thus affect the formation of iodinated disinfection byproducts during disinfection of drinking waters or wastewater effluents. In this study, a fast, sensitive and accurate method for determining these iodine species in waters was developed by derivatizing iodide and iodate to organic iodine and measuring organic iodine with a total organic iodine (TOI) measurement approach. Within this method, organo-iodine was determined directly by TOI measurement; iodide was oxidized by monochloramine to hypoiodous acid and then hypoiodous acid reacted with phenol to form organic iodine, which was determined by TOI measurement; iodate was reduced by ascorbic acid to iodide and then determined as iodide. The quantitation limit of organo-iodine or sum of organo-iodine and iodide or sum of organo-iodine, iodide and iodate was 5 μg/L as I for a 40 mL water sample (or 2.5 μg/L as I for an 80 mL water sample, or 1.25 μg/L as I for a 160 mL water sample). This method was successfully applied to the determination of iodide, iodate and organo-iodine in a variety of water samples, including tap water, seawater, urine and wastewater. The recoveries of iodide, iodate and organo-iodine were 91-109%, 90-108% and 91-108%, respectively. The concentrations and distributions of iodine species in different water samples were obtained and compared. Copyright © 2013 Elsevier Ltd. All rights reserved.

Behaviour of organic iodides under pwr accident conditions

International Nuclear Information System (INIS)

Alm, M.

1982-01-01

Laboratory experiments were performed to study the behaviour of radioactive methyl iodide under PWR loss-of-coolant conditions. The pressure relief equipment consisted of an autoclave for simulating the primary circuit and of an expansion vessel for simulating the conditions after a rupture in the reactor coolant system. After pressure relief, the composition of the CH 3 sup(127/131)I-containing steam-air mixture within the expansion vessel was analysed at 80 0 C over a period of 42 days. On the basis of the values measured and of data taken from the literature, both qualitative and quantitative assessments have been made as to the behaviour of radioactive methyl iodide in the event of loss-of-coolant accidents. (author)

Short-term responses of decomposers and vegetation to stump removal

Energy Technology Data Exchange (ETDEWEB)

Kataja-aho, S.

2011-07-01

Stump removal has become a common practice to produce raw material for bioenergy production. It was hypothesized that stump removal is an extensive and more intense disturbance for forest ecosystems (soil decomposer organisms and vegetation) compared to traditional site preparation after clear cutting. Therefore, the effects of stump harvesting on forest soil decomposers, vegetation and nutrient dynamics in undisturbed patches of the forest soil and in exposed mineral soil were compared to the effects of the traditional site preparation method, mounding. Nematodes and enchytraeids were the only decomposer groups that were directly affected (negatively) by the stump removal. Regardless of the treatment, the abundances of most of the decomposer groups were consistently lower in the exposed mineral soil than in the intact forest soil. There was 2-3 times more exposed mineral soil in stump removal sites compared to mounding sites. When this was taken into account, the decomposer community was negatively affected by the stump removal at the forest stand level. However, the greater soil disturbance at the stump harvesting sites enhanced CO{sub 2} production, net nitrogen mineralisation and nitrification. The increased N availability and the changes in microclimate due to the disturbance probably explained the vegetation increase at the stump harvested sites. Planted Norway spruce seedlings grew faster during the first two growing periods at the stump removal sites than at the mounding sites. The seedlings had high and similar ectomycorrhizal colonization rate in both treatments. In the short-term, it is probably not the resources removed in the stumps themselves, but the degree and amount of soil disturbance during the stump harvesting procedure that affects the decomposer community and its function in the clear-felled stands. (orig.)

Engaging unactivated alkyl, alkenyl and aryl iodides in visible-light-mediated free radical reactions

Science.gov (United States)

Nguyen, John D.; D'Amato, Erica M.; Narayanam, Jagan M. R.; Stephenson, Corey R. J.

2012-10-01

Radical reactions are a powerful class of chemical transformations. However, the formation of radical species to initiate these reactions has often required the use of stoichiometric amounts of toxic reagents, such as tributyltin hydride. Recently, the use of visible-light-mediated photoredox catalysis to generate radical species has become popular, but the scope of these radical precursors has been limited. Here, we describe the identification of reaction conditions under which photocatalysts such as fac-Ir(ppy)3 can be utilized to form radicals from unactivated alkyl, alkenyl and aryl iodides. The generated radicals undergo reduction via hydrogen atom abstraction or reductive cyclization. The reaction protocol utilizes only inexpensive reagents, occurs under mild reaction conditions, and shows exceptional functional group tolerance. Reaction efficiency is maintained upon scale-up and decreased catalyst loading, and the reaction time can be significantly shortened when the reaction is performed in a flow reactor.

Radiolysis of cesium iodide solutions at 35 and 85 deg C

International Nuclear Information System (INIS)

Lucas, M.

1981-09-01

An aqueous solution of cesium iodide was irradiated by the gamma rays from a cobalt 60 source with a dose rate of 0.4 Mrad/hr. At 35 deg C the iodide I - is oxidized in molecular iodine I 2 but at 85 deg C the iodate IO 3 - is obtained. The aim of this work is the study of aerosols behaviour released in accidental situation of a PWR in presence of steam [fr

Carbamazepine (Tegretol) inhibits in vivo iodide uptake and hormone synthesis in rat thyroid glands

International Nuclear Information System (INIS)

Villa, S.M.; Alexander, N.M.

1987-01-01

Decreased serum concentrations of T3 and T4 occur in patients treated with the anticonvulsant drug carbamazepine (CBZ), but with rare exception, these patients remain euthyroid. The mechanism that accounts for diminished hormone levels is unknown, and our objective was to study the direct effect of CBZ on iodide uptake and hormone synthesis in thyroid glands of CBZ-treated and pair-fed control rats. Chronic ingestion (per os) of CBZ in male rats reduced the four hour thyroid 131I-iodide uptake by approximately 60%. This inhibition occurred after the animals had received sufficient CBZ to attain plasma CBZ concentrations of 0.8 microgram/ml. Continued treatment with CBZ ranging from 560 to 800 mg/kg/day for 14 days did not result in further inhibition of iodide uptake even though the plasma CBZ concentrations had increased 6-20 fold. No inhibition of iodide uptake was apparent when the animals initially received CBZ ranging from 40 to 152 mg/kg body weight for 22 days when there were no detectable levels of plasma CBZ. Overall growth rates of CBZ-treated rats were slightly (6-10%) less than the pair-fed control animals. Plasma T4 concentrations were reduced by 18% (p less than 0.05) in the CBZ-fed animals, while T3 concentrations were diminished by 53% (p less than 0.01). CBZ appeared to alter thyroidal iodide transport because the thyroid:plasma iodide ratios were decreased by 26% in the drug-treated rats. The distribution of radioiodine in thyroidal iodoamino acids was essentially the same in both groups of rats but the absolute quantities of radioiodine were more than 2.5 times greater in the control rats. CBZ failed to inhibit peroxidase-catalyzed iodide and guaiacol oxidation in vitro

One column method to prepare 11C-labelled methyl iodide

International Nuclear Information System (INIS)

Kovacs, Z.; Priboczki, E.

1999-01-01

A new method in which the [ 11 C]methyl iodide is prepared on one alumina column is presented. A high specific surface alumina column, previously impregnated with lithium aluminium hydride solution, was used for direct trapping from the target gas and reduction into radiocomplex. The complex was then reacted on this column with HI to form [ 11 C]methyl iodide. The use of one alumina column, instead of a freezing trap, reaction vessel and separate unit for iodination, simplifies the apparatus, shortens the synthesis time and is well suitable for automation. (K.A.)

Iodide-trapping defect of the thyroid

International Nuclear Information System (INIS)

Pannall, P.R.; Steyn, A.F.; Van Reenen, O.

1978-01-01

We describe a grossly hypothyroid 50-year-old woman, mentally retarded since birth. On the basis of her history of recurrent goitre, absence of 131 I neck uptake and a low saliva/plasma 131 I ratio, congenital hypothyroidism due to a defect of the iodide-trapping mechanism was diagnosed. Other family members studied did not have the defect

Kinetic studies of the radical oxidation in gaseous phase of organic iodides and of the formation of iodine oxide particles under the simulated conditions of a nuclear reactor containment submitted to a severe accident

International Nuclear Information System (INIS)

Zhang, S.

2012-01-01

Within the framework of the research in the nuclear reactor safety field, the iodine oxides formation by organic iodides destruction in the containment has been studied with the means of the atmospheric chemistry field. The destruction kinetics and their activation energy of organic iodides by . OH and . O radical has been quantified by a Flash Photolysis system able to monitor the oxidant radicals by resonance fluorescence. Those results have been published and some of them for the first time in the literature. The mechanisms leading to the organic iodides destruction are either by a hydrogen atom abstraction, either by the formation of a complex, depending on the organic iodide involved. Then, certain kinetics reactions have been updated in the IODAIR code. Other reactions have been added based on the recent literature available. A comparison of the kinetics destruction of CH 3 I by . OH and . O with IODAIR and the global kinetics of destruction in ASTEC/IODE showed a difference of about 2 which shows the importance of these two radicals (and mainly . O) in those destruction processes. The other main path of destruction would be by electron radiation. Other radicals like . H and . N would not contribute significantly to organic iodides destruction. A sensitivity analysis highlighted that organic iodides would mostly be destroyed into iodine oxides with a almost complete conversion within a few hours. Finally, an atmospheric chamber has been used to quantify iodine oxides growth, density and composition. Under the conditions studied, their formation is fast. Particles sizes of about 200-400 nm are formed within a few hours. The main parameters influencing their growth are the relative humidity and the presence of ozone (whose function is to create . O and . OH radicals). (author)

Hydrodehalogenation of alkyl iodides with base-mediated hydrogenation and catalytic transfer hydrogenation: application to the asymmetric synthesis of N-protected α-methylamines.

Science.gov (United States)

Mandal, Pijus K; Birtwistle, J Sanderson; McMurray, John S

2014-09-05

We report a very mild synthesis of N-protected α-methylamines from the corresponding amino acids. Carboxyl groups of amino acids are reduced to iodomethyl groups via hydroxymethyl intermediates. Reductive deiodination to methyl groups is achieved by hydrogenation or catalytic transfer hydrogenation under alkaline conditions. Basic hydrodehalogenation is selective for the iodomethyl group over hydrogenolysis-labile protecting groups, such as benzyloxycarbonyl, benzyl ester, benzyl ether, and 9-fluorenyloxymethyl, thus allowing the conversion of virtually any protected amino acid into the corresponding N-protected α-methylamine.

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

21 CFR 520.763b - Dithiazanine iodide powder.

Science.gov (United States)

2010-04-01

... therapy for adult worms. (2) The drug is contraindicated in animals sensitive to dithiazanine iodide and...) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS ORAL DOSAGE FORM NEW ANIMAL DRUGS § 520.763b Dithiazanine...

Hydrogenated TiO{sub 2} nanobelts as highly efficient photocatalytic organic dye degradation and hydrogen evolution photocatalyst

Energy Technology Data Exchange (ETDEWEB)

Tian, Jian [School of Materials Science and Engineering, Shandong University of Science and Technology, Qingdao 266590 (China); State key Laboratory of Crystal Materials, Shandong University, Jinan 250100 (China); Leng, Yanhua [State key Laboratory of Crystal Materials, Shandong University, Jinan 250100 (China); Cui, Hongzhi, E-mail: cuihongzhi1965@163.com [School of Materials Science and Engineering, Shandong University of Science and Technology, Qingdao 266590 (China); Liu, Hong, E-mail: hongliu@sdu.edu.cn [State key Laboratory of Crystal Materials, Shandong University, Jinan 250100 (China)

2015-12-15

Highlights: • A facile synthesis of hydrogenated TiO{sub 2} nanobelts is reported. • Utilizing UV and visible light in photocatalytic degradation and H{sub 2} production. • The improved photocatalytic property is owe to Ti{sup 3+} ions and oxygen vacancies. - Abstract: TiO{sub 2} nanobelts have gained increasing interest because of its outstanding properties and promising applications in a wide range of fields. Here we report the facile synthesis of hydrogenated TiO{sub 2} (H-TiO{sub 2}) nanobelts, which exhibit excellent UV and visible photocatalytic decomposing of methyl orange (MO) and water splitting for hydrogen production. The improved photocatalytic property can be attributed to the Ti{sup 3+} ions and oxygen vacancies in TiO{sub 2} nanobelts created by hydrogenation. Ti{sup 3+} ions and oxygen vacancies can enhance visible light absorption, promote charge carrier trapping, and hinder the photogenerated electron–hole recombination. This work offers a simple strategy for the fabrication of a wide solar spectrum of active photocatalysts, which possesses significant potential for more efficient photodegradation, photocatalytic water splitting, and enhanced solar cells using sunlight as light source.

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

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

International Nuclear Information System (INIS)

Holm, J.; Glaenneskog, H.; Ekberg, C.; Kaerkelae, T.; Auvinen, A.

2010-05-01

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

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.

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

CONTAIN code calculations of the effects on the source term of CsI to I/sub 2/ conversion due to severe hydrogen burns

International Nuclear Information System (INIS)

Valdez, G.D.; Williams, D.C.

1986-01-01

In experiments conducted at Sandia National Laboratories large amounts of elemental iodine were produced when CsI-Al 2 O 3 aerosol was exposed to hydrogen/air combustion. To evaluate some of the implications of the iodide conversion (observed to occur with up to 75% efficiency) for the severe accident source term, computational simulations of representative accident sequences were conducted with the CONTAIN code. The following conclusions can be drawn from this preliminary source term assessment: (1) If the containment sprays are inoperative during the accident, or failed by the hydrogen burn, the late-time source term is almost tripled when the iodide is converted to I 2 . (2) With the sprays active, the amount released without conversion of the CsI aerosol is 63% higher than for the case when conversion occurs. (3) For the case where CsI is converted to I 2 continued operation of the sprays reduces the release by a factor of 40, relative to the case in which the sprays fail at the time of the hydrogen burn. When there is no conversion, the reduction factor for continued spray operation is about a factor of 9, relative to the failed spray case

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...

FY-2016 Methyl Iodide Higher NOx 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)

2016-09-01

Deep-bed methyl iodide adsorption testing has continued in Fiscal Year 2016 under the Department of Energy (DOE) Fuel Cycle Technology (FCT) Program Offgas Sigma Team to further research and advance the technical maturity of solid sorbents for capturing iodine-129 in off-gas streams during used nuclear fuel reprocessing. Adsorption testing with higher levels of NO (approximately 3,300 ppm) and NO2 (up to about 10,000 ppm) indicate that high efficiency iodine capture by silver aerogel remains possible. Maximum iodine decontamination factors (DFs, or the ratio of iodine flowrate in the sorbent bed inlet gas compared to the iodine flowrate in the outlet gas) exceeded 3,000 until bed breakthrough rapidly decreased the DF levels to as low as about 2, when the adsorption capability was near depletion. After breakthrough, nearly all of the uncaptured iodine that remains in the bed outlet gas stream is no longer in the form of the original methyl iodide. The methyl iodide molecules are cleaved in the sorbent bed, even after iodine adsorption is no longer efficient, so that uncaptured iodine is in the form of iodine species soluble in caustic scrubber solutions, and detected and reported here as diatomic I2. The mass transfer zone depths were estimated at 8 inches, somewhat deeper than the 2-5 inch range estimated for both silver aerogels and silver zeolites in prior deep-bed tests, which had lower NOx levels. The maximum iodine adsorption capacity and silver utilization for these higher NOx tests, at about 5-15% of the original sorbent mass, and about 12-35% of the total silver, respectively, were lower than for trends from prior silver aerogel and silver zeolite tests with lower NOx levels. Additional deep-bed testing and analyses are recommended to expand the database for organic iodide adsorption and increase the technical maturity if iodine adsorption processes.

Hydrogen Peroxide: A Key Chemical for Today's Sustainable Development.

Science.gov (United States)

Ciriminna, Rosaria; Albanese, Lorenzo; Meneguzzo, Francesco; Pagliaro, Mario

2016-12-20

The global utilization of hydrogen peroxide, a green oxidant that decomposes in water and oxygen, has gone from 0.5 million tonnes per year three decades ago to 4.5 million tonnes per year in 2014, and is still climbing. With the aim of expanding the utilization of this eminent green chemical across different industrial and civil sectors, the production and use of hydrogen peroxide as a green industrial oxidant is reviewed herein to provide an overview of the explosive growth of its industrial use over the last three decades and of the state of the art in its industrial manufacture, with important details of what determines the viability of the direct production from oxygen and hydrogen compared with the traditional auto-oxidation process. © 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

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. Copyright © 2016 Elsevier Ltd. All rights reserved.

Capture of organic iodides from nuclear waste by metal-organic framework-based molecular traps.

Science.gov (United States)

Li, Baiyan; Dong, Xinglong; Wang, Hao; Ma, Dingxuan; Tan, Kui; Jensen, Stephanie; Deibert, Benjamin J; Butler, Joseph; Cure, Jeremy; Shi, Zhan; Thonhauser, Timo; Chabal, Yves J; Han, Yu; Li, Jing

2017-09-07

Effective capture of radioactive organic iodides from nuclear waste remains a significant challenge due to the drawbacks of current adsorbents such as low uptake capacity, high cost, and non-recyclability. We report here a general approach to overcome this challenge by creating radioactive organic iodide molecular traps through functionalization of metal-organic framework materials with tertiary amine-binding sites. The molecular trap exhibits a high CH 3 I saturation uptake capacity of 71 wt% at 150 °C, which is more than 340% higher than the industrial adsorbent Ag 0 @MOR under identical conditions. These functionalized metal-organic frameworks also serve as good adsorbents at low temperatures. Furthermore, the resulting adsorbent can be recycled multiple times without loss of capacity, making recyclability a reality. In combination with its chemical and thermal stability, high capture efficiency and low cost, the adsorbent demonstrates promise for industrial radioactive organic iodides capture from nuclear waste. The capture mechanism was investigated by experimental and theoretical methods.Capturing radioactive organic iodides from nuclear waste is important for safe nuclear energy usage, but remains a significant challenge. Here, Li and co-workers fabricate a stable metal-organic framework functionalized with tertiary amine groups that exhibits high capacities for radioactive organic iodides uptake.

Capture of organic iodides from nuclear waste by metal-organic framework-based molecular traps

KAUST Repository

Li, Baiyan

2017-09-01

Effective capture of radioactive organic iodides from nuclear waste remains a significant challenge due to the drawbacks of current adsorbents such as low uptake capacity, high cost, and non-recyclability. We report here a general approach to overcome this challenge by creating radioactive organic iodide molecular traps through functionalization of metal-organic framework materials with tertiary amine-binding sites. The molecular trap exhibits a high CH3I saturation uptake capacity of 71 wt% at 150 °C, which is more than 340% higher than the industrial adsorbent Ag0@MOR under identical conditions. These functionalized metal-organic frameworks also serve as good adsorbents at low temperatures. Furthermore, the resulting adsorbent can be recycled multiple times without loss of capacity, making recyclability a reality. In combination with its chemical and thermal stability, high capture efficiency and low cost, the adsorbent demonstrates promise for industrial radioactive organic iodides capture from nuclear waste. The capture mechanism was investigated by experimental and theoretical methods.Capturing radioactive organic iodides from nuclear waste is important for safe nuclear energy usage, but remains a significant challenge. Here, Li and co-workers fabricate a stable metal-organic framework functionalized with tertiary amine groups that exhibits high capacities for radioactive organic iodides uptake.

Simultaneous detection of iodine and iodide on boron doped diamond electrodes.

Science.gov (United States)

Fierro, Stéphane; Comninellis, Christos; Einaga, Yasuaki

2013-01-15

Individual and simultaneous electrochemical detection of iodide and iodine has been performed via cyclic voltammetry on boron doped diamond (BDD) electrodes in a 1M NaClO(4) (pH 8) solution, representative of typical environmental water conditions. It is feasible to compute accurate calibration curve for both compounds using cyclic voltammetry measurements by determining the peak current intensities as a function of the concentration. A lower detection limit of about 20 μM was obtained for iodide and 10 μM for iodine. Based on the comparison between the peak current intensities reported during the oxidation of KI, it is probable that iodide (I(-)) is first oxidized in a single step to yield iodine (I(2)). The latter is further oxidized to obtain IO(3)(-). This technique, however, did not allow for a reasonably accurate detection of iodate (IO(3)(-)) on a BDD electrode. Copyright © 2012 Elsevier B.V. All rights reserved.

Application of rice rhizosphere microflora for hydrogen production from apple pomace

Energy Technology Data Exchange (ETDEWEB)

Doi, Tetsuya [Institute for Sustainable Agro-ecosystem Services (ISAS), Graduate School of Agriculture and Life Sciences, The University of Tokyo, Nishitokyo, Tokyo 188-0002 (Japan); Nishihara Environment Technology Inc., Tokyo 108-0023 (Japan); Matsumoto, Hisami [Nishihara Environment Technology Inc., Tokyo 108-0023 (Japan); Abe, Jun [AE-Bio, Graduate School of Agriculture and Life Sciences, The University of Tokyo, Tokyo 113-8657 (Japan); Morita, Shigenori [Institute for Sustainable Agro-ecosystem Services (ISAS), Graduate School of Agriculture and Life Sciences, The University of Tokyo, Nishitokyo, Tokyo 188-0002 (Japan)

2010-07-15

The combination of substrate materials and bacteria is an important factor affecting conversion technology for biological hydrogen production. We performed anaerobic hydrogen fermentation of apple pomace wastes using rhizosphere bacterial microflora of rice as the parent inoculum. In the vial test, the optimal condition for hydrogen fermentation was initial pH 6.0, 35 C, and 73.4 g pomace per liter of medium (equivalent to 10 g-hexose/L). In the batch experiment (pH 6.0, temperature 35 C) the hydrogen yield reached 2.3 mol-H{sub 2}/mol-hexose. The time course of biogas production and PCR-DGGE analysis suggest that Clostridium spp. decomposed degradable carbohydrates rapidly and a part of the refractory carbohydrate (e.g. pectin) gradually in the apple pomace slurry. In addition to hydrogen, volatile fatty acids (VFAs) were produced in the anaerobic fermentation of apple pomace, which can be a substrate for methane fermentation. The rice rhizosphere can be a promising source of inoculum bacteria for hydrogen fermentation in combination with plant material waste like apple pomace. (author)

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.

Research on High Sensitive D-Shaped FBG Hydrogen Sensors in Power Transformer Oil.

Science.gov (United States)

Luo, Ying-Ting; Wang, Hong-Bin; Ma, Guo-Ming; Song, Hong-Tu; Li, Chengrong; Jiang, Jun

2016-10-04

Dissolved hydrogen is a symbol gas decomposed by power transformer oil for electrical faults such as overheat or partial discharges. A novel D-shaped fiber Bragg grating (D-FBG) sensor is herein proposed and was fabricated with magnetron sputtering to measure the dissolved hydrogen concentration in power transformer oil in this paper. Different from the RI (refractive index)-based effect, D-FBG in this case is sensitive to curvature caused by stress from sensing coating, leading to Bragg wavelength shifts accordingly. The relationship between the D-FBG wavelength shift and dissolved hydrogen concentration in oil was measured experimentally in the laboratory. The detected sensitivity could be as high as 1.96 μL/L at every 1-pm wavelength shift. The results proved that a simple, polished FBG-based hydrogen sensor provides a linear measuring characteristic in the range of low hydrogen concentrations in transformer oil. Moreover, the stable hydrogen sensing performance was investigated by X-ray diffraction analysis.

Research on High Sensitive D-Shaped FBG Hydrogen Sensors in Power Transformer Oil

Directory of Open Access Journals (Sweden)

Ying-Ting Luo

2016-10-01

Full Text Available Dissolved hydrogen is a symbol gas decomposed by power transformer oil for electrical faults such as overheat or partial discharges. A novel D-shaped fiber Bragg grating (D-FBG sensor is herein proposed and was fabricated with magnetron sputtering to measure the dissolved hydrogen concentration in power transformer oil in this paper. Different from the RI (refractive index-based effect, D-FBG in this case is sensitive to curvature caused by stress from sensing coating, leading to Bragg wavelength shifts accordingly. The relationship between the D-FBG wavelength shift and dissolved hydrogen concentration in oil was measured experimentally in the laboratory. The detected sensitivity could be as high as 1.96 μL/L at every 1-pm wavelength shift. The results proved that a simple, polished FBG-based hydrogen sensor provides a linear measuring characteristic in the range of low hydrogen concentrations in transformer oil. Moreover, the stable hydrogen sensing performance was investigated by X-ray diffraction analysis.

[DNA extraction from decomposed tissue by double-digest and magnetic beads methods].

Science.gov (United States)

Yang, Dian; Liu, Chao; Liu, Hong

2011-12-01

To study the effect of the double-digest and magnetic beads method for DNA extraction from 3 types of decomposed tissues. DNA of cartilages, nails and joint capsule in 91 highly decomposed corpses which had not been extracted by common magnetic beads method, were prepared with the double-digest and magnetic beads methods, and quantified with Quantifiler kit, followed by amplification with Sinofiler kit or Minifiler kit. DNA concentration extracted from the 91 highly decomposed cartilages, nails and joint capsule samples was 0-0.225 ng/microL. Sixty-two samples whose DNA concentration were more than 0.020 ng/microL had obtained 9 or more STR loci successfully. The detection rate was 68.13%. The successful rate of STR genotyping for the 3 types of decomposed tissues can be significantly improved by the double-digest and magnetic beads methods.

Solvent effect on the rate and equilibrium of reaction between 10-phenylphenoxarsine and methyl iodide

International Nuclear Information System (INIS)

Gavrilov, V.I.; Gumerov, N.S.; Rakhmatullin, R.R.

1990-01-01

Effect of solvent nature on nucleophilic capacity of three-coordinated arsenic and the equilibrium state of 10-phenylphenoxarsine (PA) reaction with methyl iodide are studied. Kinetic investigations are carried out by the conductometry at 24,35,45 deg C. It is established that quaternization of PA with methyl iodide when substituting a solvent (ketone for alcohol) increases 3-14 times with simultaneous growth of the activation energy value. When transforming from aprotic solvents to protic ones PA interaction equilibrium with methyl iodide shifts to the side of arsonic salt formation

Optical hydrogen sensors based on metal-hydrides

Science.gov (United States)

Slaman, M.; Westerwaal, R.; Schreuders, H.; Dam, B.

2012-06-01

For many hydrogen related applications it is preferred to use optical hydrogen sensors above electrical systems. Optical sensors reduce the risk of ignition by spark formation and are less sensitive to electrical interference. Currently palladium and palladium alloys are used for most hydrogen sensors since they are well known for their hydrogen dissociation and absorption properties at relatively low temperatures. The disadvantages of palladium in sensors are the low optical response upon hydrogen loading, the cross sensitivity for oxygen and carbon, the limited detection range and the formation of micro-cracks after some hydrogen absorption/desorption cycles. In contrast to Pd, we find that the use of magnesium or rear earth bases metal-hydrides in optical hydrogen sensors allow tuning of the detection levels over a broad pressure range, while maintaining a high optical response. We demonstrate a stable detection layer for detecting hydrogen below 10% of the lower explosion limit in an oxygen rich environment. This detection layer is deposited at the bare end of a glass fiber as a micro-mirror and is covered with a thin layer of palladium. The palladium layer promotes the hydrogen uptake at room temperature and acts as a hydrogen selective membrane. To protect the sensor for a long time in air a final layer of a hydrophobic fluorine based coating is applied. Such a sensor can be used for example as safety detector in automotive applications. We find that this type of fiber optic hydrogen sensor is also suitable for hydrogen detection in liquids. As example we demonstrate a sensor for detecting a broad range of concentrations in transformer oil. Such a sensor can signal a warning when sparks inside a high voltage power transformer decompose the transformer oil over a long period.

A note on arbitrarily vertex decomposable graphs

Directory of Open Access Journals (Sweden)

Antoni Marczyk

2006-01-01

Full Text Available A graph \\(G\\ of order \\(n\\ is said to be arbitrarily vertex decomposable if for each sequence \\((n_{1},\\ldots,n_k\\ of positive integers such that \\(n_{1}+\\ldots+n_{k}=n\\ there exists a partition \\((V_{1},\\ldots,V_{k}\\ of the vertex set of \\(G\\ such that for each \\(i \\in \\{1,\\ldots,k\\}\\, \\(V_{i}\\ induces a connected subgraph of \\(G\\ on \\(n_i\\ vertices. In this paper we show that if \\(G\\ is a two-connected graph on \\(n\\ vertices with the independence number at most \\(\\lceil n/2\\rceil\\ and such that the degree sum of any pair of non-adjacent vertices is at least \\(n-3\\, then \\(G\\ is arbitrarily vertex decomposable. We present another result for connected graphs satisfying a similar condition, where the bound \\(n-3\\ is replaced by \\(n-2\\.

Synthesis and evaluation of iodide uptake inhibitors in thyroid gland

International Nuclear Information System (INIS)

Lacotte, Pierre

2012-01-01

This work was intended to discover small organic molecules acting as iodide uptake inhibitors in thyroid cells. These compounds can indeed be derivatized into biochemical probes for further characterization of proteins involved in iodide transport mechanisms. On the long term, these inhibitors also appear as attractive drug candidates for treatment of thyroid pathologies or radioprotection against iodine isotopes. A similar strategy was adopted for both of the two inhibitor families. First, we synthesized a chemical library of around 100 analogues; we measured their IC50 against iodide uptake in FRTL-5 cells to get structure-activity relationships. Absolute configuration of stereo-genic centers was also investigated, and a preferential stereochemistry was found to be responsible for activity. From this basis, around twenty 'second-generation' analogues were synthesized by combining fragments contributing to biological activity. Biological evaluation indicated that nine were very potent inhibitors, with IC50 ≤ 6 nM and satisfying physicochemical properties required for drug candidates. Finally, one photoactivatable biotinylated probe was developed in each family and used for photoaffinity labeling. Several specifically labeled proteins are still under identification and constitute new potential therapeutic targets. (author)

The method of determination of micro quantities of labelled iodide in Na125 I carrier free solution

International Nuclear Information System (INIS)

Kholbaev, A.Kh.; Shilin, E.A.

1996-01-01

The analytical method was elaborated with the purpose to increase detection limit and radiation safety of labelled iodide determination. The method includes oxidation of iodide by iodate in diluted sulphur acid solution with molar concentration 0,03-0,04/moles/litre at molar ratio of iodide to iodate I - :IO - 3 1:12,5. The extraction of I 2 produced is done by toluene. (author)

Study on the Electrochemical Behavior of Iodide at Platinum Electrode in Potassium Chlorate Solution

Energy Technology Data Exchange (ETDEWEB)

Jung, Sang Hyuk; Yeon, Jei Won; Song, Kyu Seok [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2012-05-15

Radioactive iodine-131, is one of the most hazardous fission products which could be released from fuels of nuclear reactors during the severe accident of nuclear power plants. Due to its high radioactivity, high fission yield (2.8%) and hazardous biological effects, the behavior of iodine has been taken interests in many research groups. Iodine is known to be released from the fuels as a cesium iodide form, CsI. And, as nuclear fuels are mostly placed in the water pool, it is easily dissolved in the water after released from the fuels. In water, iodide anion could be oxidized into molecular iodine. As the molecular iodine is a volatile species and the oxidizing rate is affected by many environmental facts such as pH, radiolysis products and temperature, the oxidation reaction of the iodide ion has been considered as an important chemical reaction related to the severe accident of nuclear power plants In present work, the electrochemical behavior of iodide anion was observed by using cyclic voltammetric technique in potassium chlorate solutions. We observed two different oxidation waves in the oxidation potential region. From the comparison with the previous reported results, one is regarded as the oxidation of iodide into molecular iodine. The other is evaluated to be the formation of high-valent iodine-containing compounds

Gamma-ray radiolysis of methyl iodide in air, in presence of water vapor

International Nuclear Information System (INIS)

Aubert, F.

2002-03-01

This work aims at modelling the processes involved in gamma-radiolysis of methyl iodide diluted in air in presence of steam. It is to determine quantitative and qualitative information, to quantify the importance of the organic iodides destruction in case of a nuclear reactor accident. The main data for radiochemistry and iodine compounds (I x O y and INO x ) formation were reviewed and analysed. Literature data about air products radiolysis reactivity towards I 2 and CH 3 I were used to develop a mechanistic model for methyl iodide destruction in the gas phase under gamma irradiation. An ab initio study was realised for a better understanding of atomic nitrogen ( 4 S and 2 D) reactivity towards CH 3 I. The model was tested on the available experimental data and constitute a way to investigate the main processus involved in methyl iodide destruction. For the low CH 3 I concentrations, about 10 -7 - 10 -8 mol.dm -3 , N and e - are mainly responsible for the destruction. I 2 O 4 (highest iodine oxide in the model) and IONO 2 are the main resulting iodinated' compounds. (author)

A portable multi-syringe flow system for spectrofluorimetric determination of iodide in seawater.

Science.gov (United States)

Frizzarin, Rejane M; Aguado, Enrique; Portugal, Lindomar A; Moreno, Daniel; Estela, José M; Rocha, Fábio R P; Cerdà, Victor

2015-11-01

A miniaturized analyzer encompassing a poly(methyl methacrylate) chip with integrated spectrofluorimetric detection and solutions propelling by a multi-syringe module is proposed. Iodide was determined through its catalytic effect on the reaction between Ce(IV) and As(III). Matrix isopotential synchronous fluorescence was explored to set the excitation and emission wavelengths. A two-level full factorial design allowed to evaluate the significance of variables (Ce(IV), As(III) and H2SO4 concentrations) and their interaction effects in the experimental domain. A Doehlert Matrix was applied to identify the critical values. The optimized procedure showed a linear response from 1 to 100 μg L(-1) (S=53.7+2.61C, in which S is the net fluorescence and C is iodide concentration in μg L(-1)). Detection limit, coefficient of variation (n=6) and sampling rate were estimated at 0.3 μg L(-1), 0.8% and 20 h(-1), respectively. Recoveries within 90-117% were estimated for iodide spiked to seawater samples. The proposed procedure stands out because of the portability, robustness, and simplicity for in-field analysis of iodide in seawater. Copyright © 2015 Elsevier B.V. All rights reserved.

Decomposition of methane hydrate for hydrogen production using microwave and radio frequency in-liquid plasma methods

International Nuclear Information System (INIS)

Rahim, Ismail; Nomura, Shinfuku; Mukasa, Shinobu; Toyota, Hiromichi

2015-01-01

This research involves two in-liquid plasma methods of methane hydrate decomposition, one using radio frequency wave (RF) irradiation and the other microwave radiation (MW). The ultimate goal of this research is to develop a practical process for decomposition of methane hydrate directly at the subsea site for fuel gas production. The mechanism for methane hydrate decomposition begins with the dissociation process of methane hydrate formed by CH_4 and water. The process continues with the simultaneously occurring steam methane reforming process and methane cracking reaction, during which the methane hydrate is decomposed releasing CH_4 into H_2, CO and other by-products. It was found that methane hydrate can be decomposed with a faster rate of CH_4 release using microwave irradiation over that using radio frequency irradiation. However, the radio frequency plasma method produces hydrogen with a purity of 63.1% and a CH conversion ratio of 99.1%, which is higher than using microwave plasma method which produces hydrogen with a purity of 42.1% and CH_4 conversion ratio of 85.5%. - Highlights: • The decomposition of methane hydrate is proposed using plasma in-liquid method. • Synthetic methane hydrate is used as the sample for decomposition in plasma. • Hydrogen can be produced from decomposition of methane hydrate. • Hydrogen purity is higher when using radio frequency stimulation.

Extraction and determination of hydrogen in uranium and zirconium

International Nuclear Information System (INIS)

Champeix, L.; Coblence, G.; Darras, R.

1959-01-01

The method of desorption under vacuum at high temperatures in the solid phase, which gives good results in the case of steels, has been applied to uranium and zirconium. In these two metals hydrogen is found mainly in the form of hydride. It is chiefly a question of determining the most suitable temperature and the heating time necessary to obtain an almost total extraction of hydrogen. Two considerations must be taken into account in the choice of temperature. It should be such that on the one hand the hydride decomposes rapidly and completely at the reduced pressure applied, and on the other hand the diffusion of hydrogen through the metal takes place fairly quickly. The apparatus and the method used are described; systematic tests have led to the adoption of temperatures of 650 deg. C for uranium and 1050 deg. C for zirconium. (author) [fr

Effect of iodide on glucose oxidation and 32P incorporation into phospholipids stimulated by different agents in dog thyroid slices

International Nuclear Information System (INIS)

Tseng, F.Y.; Rani, C.S.; Field, J.B.

1989-01-01

Since iodide (I-) inhibits TSH stimulation of cAMP formation, which mediates most of the effects of the hormone, it has been assumed that this accounts for the inhibitory action of iodide on the thyroid. However, TSH stimulation of 32P incorporation into phospholipids and stimulation of thyroid metabolism by other agonists, such as carbachol, phorbol esters, and ionophore A23187, is not cAMP mediated. The present studies examined the effect of iodide on stimulation of glucose oxidation and 32P incorporation into phospholipids by TSH and other agonists to determine if the inhibition of cAMP formation was responsible for the action of iodide. Preincubation of dog thyroid slices for 1 h with iodide (10(-4) M) inhibited TSH-, (Bu)2cAMP-, carbachol-, methylene blue-, 12-O-tetradecanoyl phorbol-13-acetate-, ionophore A23187-, prostaglandin E1-, and cholera toxin-stimulated glucose oxidation. I- also inhibited the stimulation by TSH, 12-O-tetradecanoyl phorbol-13-acetate, carbachol, and ionophore A23187 of 32P incorporation into phospholipids. The inhibition was similar whether iodide was added 2 h before or simultaneously with the agonist. I- itself sometimes stimulated basal glucose oxidation, but had no effect on basal 32P incorporation into phospholipids. The effects of iodide on basal and agonist-stimulated thyroid metabolism were blocked by methimazole (10(-3) M). When dog thyroid slices were preloaded with 32PO4 or [1-14C]glucose, the iodide inhibition of agonist stimulation disappeared, suggesting that the effect of iodide involves the transport process. In conclusion, I- inhibited stimulation of glucose oxidation and 32P incorporation into phospholipids by all agonists, indicating that the effect is independent of the cAMP system and that iodide autoregulation does not only involve this system. Oxidation and organification of iodide are necessary for the inhibition

3.2. Antibacterial activity of ethynyl-piperidol polymers and their three-iodides

International Nuclear Information System (INIS)

Khalikov, D.Kh.

2012-01-01

The antibacterial activity of ethynyl-piperidol polymers and their three-iodides was studied. The antibacterial films based on iodine with copolymer N-vinyl pyrrolidone, methylmethacrylate and butyl acrylate were obtained. It was found that samples containing 9-10% of iodine in copolymer have the antiseptic properties. The antibacterial properties of three-iodides grafted nitrogen containing polymers with cellulose fibrous materials were considered. The membrane-active properties of homo- and copolymers of ethynyl piperidol derivatives were considered as well.

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

International Nuclear Information System (INIS)

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

1986-01-01

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 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 2 ingestion, it seems that ClO 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

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

International Nuclear Information System (INIS)

Douglas, S.; McGregor Elsa; Ariesanti Bridget Corcoran

2004-01-01

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

Multicompartmental model for iodide, thyroxine, and triiodothyronine metabolism in normal and spontaneously hyperthyroid cats

Energy Technology Data Exchange (ETDEWEB)

Hays, M.T.; Broome, M.R.; Turrel, J.M.

1988-06-01

A comprehensive multicompartmental kinetic model was developed to account for the distribution and metabolism of simultaneously injected radioactive iodide (iodide*), T3 (T3*), and T4 (T4*) in six normal and seven spontaneously hyperthyroid cats. Data from plasma samples (analyzed by HPLC), urine, feces, and thyroid accumulation were incorporated into the model. The submodels for iodide*, T3*, and T4* all included both a fast and a slow exchange compartment connecting with the plasma compartment. The best-fit iodide* model also included a delay compartment, presumed to be pooling of gastrosalivary secretions. This delay was 62% longer in the hyperthyroid cats than in the euthyroid cats. Unexpectedly, all of the exchange parameters for both T4 and T3 were significantly slowed in hyperthyroidism, possibly because the hyperthyroid cats were older. None of the plasma equivalent volumes of the exchange compartments of iodide*, T3*, or T4* was significantly different in the hyperthyroid cats, although the plasma equivalent volume of the fast T4 exchange compartments were reduced. Secretion of recycled T4* from the thyroid into the plasma T4* compartment was essential to model fit, but its quantity could not be uniquely identified in the absence of multiple thyroid data points. Thyroid secretion of T3* was not detectable. Comparing the fast and slow compartments, there was a shift of T4* deiodination into the fast exchange compartment in hyperthyroidism. Total body mean residence times (MRTs) of iodide* and T3* were not affected by hyperthyroidism, but mean T4* MRT was decreased 23%. Total fractional T4 to T3 conversion was unchanged in hyperthyroidism, although the amount of T3 produced by this route was increased nearly 5-fold because of higher concentrations of donor stable T4.

Multicompartmental model for iodide, thyroxine, and triiodothyronine metabolism in normal and spontaneously hyperthyroid cats

International Nuclear Information System (INIS)

Hays, M.T.; Broome, M.R.; Turrel, J.M.

1988-01-01

A comprehensive multicompartmental kinetic model was developed to account for the distribution and metabolism of simultaneously injected radioactive iodide (iodide*), T3 (T3*), and T4 (T4*) in six normal and seven spontaneously hyperthyroid cats. Data from plasma samples (analyzed by HPLC), urine, feces, and thyroid accumulation were incorporated into the model. The submodels for iodide*, T3*, and T4* all included both a fast and a slow exchange compartment connecting with the plasma compartment. The best-fit iodide* model also included a delay compartment, presumed to be pooling of gastrosalivary secretions. This delay was 62% longer in the hyperthyroid cats than in the euthyroid cats. Unexpectedly, all of the exchange parameters for both T4 and T3 were significantly slowed in hyperthyroidism, possibly because the hyperthyroid cats were older. None of the plasma equivalent volumes of the exchange compartments of iodide*, T3*, or T4* was significantly different in the hyperthyroid cats, although the plasma equivalent volume of the fast T4 exchange compartments were reduced. Secretion of recycled T4* from the thyroid into the plasma T4* compartment was essential to model fit, but its quantity could not be uniquely identified in the absence of multiple thyroid data points. Thyroid secretion of T3* was not detectable. Comparing the fast and slow compartments, there was a shift of T4* deiodination into the fast exchange compartment in hyperthyroidism. Total body mean residence times (MRTs) of iodide* and T3* were not affected by hyperthyroidism, but mean T4* MRT was decreased 23%. Total fractional T4 to T3 conversion was unchanged in hyperthyroidism, although the amount of T3 produced by this route was increased nearly 5-fold because of higher concentrations of donor stable T4

Hydrogenation study of suction-cast Ti{sub 40}Zr{sub 40}Ni{sub 20} quasicrystal

Energy Technology Data Exchange (ETDEWEB)

Huang, Huogen; Li, Rong; Yin, Chen; Zheng, Shaotao; Zhang, Pengcheng [National Key Laboratory for Surface Physics and Chemistry, P.O. Box 718-35, Mian Yang 621907, Sichuan (China)

2008-09-15

Suction casting was predicted to be an usable method for improving the hydriding kinetics of Ti/Zr-based icosahedral quasicrystals (IQCs) in our previous work. To further determine it, a suction-cast Ti{sub 40}Zr{sub 40}Ni{sub 20} IQC alloy was used for hydrogenation studies by Pressure Composition Isotherm (PCI) and Temperature Programmed Desorption (TPD) techniques. The results showed that, this alloy absorbed hydrogen rapidly with obvious hydrogen pressure plateau and some reversibility, however, displayed very limited hydrogen capacity (about 0.7 wt.%) and low equilibrium pressure. After several hydrogenation/dehydrogenation cycles, the IQC structure transformed into two hydride phases, ZrH{sub 2-x} and one unknown, both of which decomposed at above 600 C, suggesting high thermo-stability for them. On the whole, indeed the suction-casting method can increase the hydrogen absorption rate of Ti/Zr-based IQCs, however, the hydrogenation properties of the Ti{sub 40}Zr{sub 40}Ni{sub 20} IQC alloy still need a mighty advancement. (author)

Scalable Domain Decomposed Monte Carlo Particle Transport

Energy Technology Data Exchange (ETDEWEB)

O' Brien, Matthew Joseph [Univ. of California, Davis, CA (United States)

2013-12-05

In this dissertation, we present the parallel algorithms necessary to run domain decomposed Monte Carlo particle transport on large numbers of processors (millions of processors). Previous algorithms were not scalable, and the parallel overhead became more computationally costly than the numerical simulation.

Electronic properties and Compton profiles of silver iodide

Indian Academy of Sciences (India)

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 ...

Developments in mercuric iodide gamma ray imaging

Energy Technology Data Exchange (ETDEWEB)

Patt, B E; Beyerle, A G; Dolin, R C; Ortale, C [EG and G Energy Measurements, Inc., Goleta, CA (USA). Santa Barbara Operations

1989-11-01

A mercuric iodide (HgI{sub 2}) gamma ray imaging array and camera system previously described have been characterized for spatial and energy resolution. Based on these data a new camera is being developed to more fully exploit the potential of the array. Characterization results and design criteria for the new camera will be presented. (orig.).

Synergistic Effect of Azadirachta Indica Extract and Iodide Ions on the Corrosion Inhibition of Aluminium in Acid Media

Energy Technology Data Exchange (ETDEWEB)

Arab, S. T.; Al- Turkustani, A. M.; Al- Dhahiri, R. H. [King Abd El- Aziz University, Jeddah (Saudi Arabia)

2008-06-15

The synergistic action caused by iodide ions on the corrosion inhibition of aluminium (Al) in 0.5 M HCl in the presence of Azadirachta Indica (AZI) plant extract has been investigated using potintiodynamic polarization and impedance techniques. It is found that AZI extract inhibits the corrosion of aluminium in 0.5 M HCl. The inhibition efficiency increases with the increase in AZI extract concentration, until 24% v/v of AZI extract, then Inh.% is decreased with father increase in AZI extract concentration. The adsorption of this extract in the studied concentration is found to obey Frewendlish adsorption isotherm. The addition of iodide ions enhances the inhibition efficiency to a considerable extent. The increase in Inh.% values in presence of fixed concentration of iodide ions indicates that AZI extract forms an insoluble complex at lower AZI extract concentrations by undergoing a joint adsorption. But at higher concentrations of AZI extract, competitive adsorption is found between iodide ions and the formed complex leading to less Inh.%. The Inh.% decreased in presence of iodide ions with AZI extract than in presence of AZI extract alone at all studied iodide concentrations. The synergism parameter S {sub θ} is defined and calculated from surface coverage values. This parameter in the case of AZI extract is found to be more than unity, indicating that the enhanced inhibition efficiency caused by the addition of iodide ions.

The method of determination of micro quantities of labeled iodide in carrier free Na125 solution

International Nuclear Information System (INIS)

Kholbaev, A.Kh.; Shilin, E.A.

1996-01-01

The method of determination of microquantities of labelled iodide in Na 125 carrier-free solution was elaborated. This method permits to increase the sensitivity and radiation protection of the determination of labeled iodide. It includes oxidation of iodide by iodate in diluted sulphuric acid with molar concentration 0,03-0,04 mole/l. The extraction of I 2 is made by toluene. The coloured solution is made and optical density is measured at λ=640 nm at the 10 mm optical path .(A.A.D.)

Photochemical versus biological production of methyl iodide during Meteor 55

Science.gov (United States)

Richter, U.; Wallace, D.

2003-04-01

The flux of methyl iodide from sea to air represents the largest flux of iodine from the ocean to the atmosphere. Surface water concentrations and hence fluxes are particularly high in tropical regions. This flux may be responsible for the enrichment of iodine in the marine aerosol and may contribute to important processes in the marine boundary layer, including particle formation. Methyl iodide is commonly referred to as a biogenic gas, with both macroalgae and phytoplankton identified as important sources. On the other hand experimental and field data have shown the importance of photochemical production that is not necessarily associated directly with biological activity. During the Meteor cruise 55 along 11°N in the tropical Atlantic Ocean, a series of experiments were conducted to examine the biological vs. photochemical production of methyl iodide. A total of eight separate experiments were conducted. Production of CH3I in quartz glass flasks during 24 hour incubations (dark and natural sunlight) was measured under three experimental treatments: untreated seawater, filtered seawater (0.1 um pore size filter to exclude most phytoplankton and bacteria), and seawater that was poisoned with mercuric chloride. There were two clear findings from these experiments: (1) methyl iodide production was significantly higher in all the incubations that were exposed to the light than in the dark incubations; (2) there was no significant difference between CH3I production under the three experimental treatments. These results argue very strongly for the primary importance of photochemical production of CH3I as opposed to biogenic production at least for the tropical open ocean surface waters. Further experiments are required to investigate the reactants involved, their sources, the wavelength and depth dependence of production, etc. as well as (possibly related) sink processes.

A model for additive transport in metal halide lamps containing mercury and dysprosium tri-iodide

NARCIS (Netherlands)

Beks, M.L.; Haverlag, M.; Mullen, van der J.J.A.M.

2008-01-01

The distribution of additives in a metal halide lamp is examined through numerical modelling. A model for a lamp containing sodium iodide additives has been modified to study a discharge containing dysprosium tri-iodide salts. To study the complex chemistry the method of Gibbs minimization is used

Preparation and Hydrogen Storage Properties of Mg-Rich Mg-Ni Ultrafine Particles

Directory of Open Access Journals (Sweden)

Jianxin Zou

2012-01-01

Full Text Available In the present work, Mg-rich Mg-Ni ultrafine powders were prepared through an arc plasma method. The phase components, microstructure, and hydrogen storage properties of the powders were carefully investigated. It is found that Mg2Ni and MgNi2 could be obtained directly from the vapor state reactions between Mg and Ni, depending on the local vapor content in the reaction chamber. A nanostructured MgH2 + Mg2NiH4 hydrogen storage composite could be generated after hydrogenation of the Mg-Ni ultrafine powders. After dehydrogenation, MgH2 and Mg2NiH4 decomposed into nanograined Mg and Mg2Ni, respectively. Thermogravimetry/differential scanning calorimetry (TG/DSC analyses showed that Mg2NiH4 phase may play a catalytic role in the dehydriding process of the hydrogenated Mg ultrafine particles.

Process for synthesis of ammonia borane for bulk hydrogen storage

Science.gov (United States)

Autrey, S Thomas [West Richland, WA; Heldebrant, David J [Richland, WA; Linehan, John C [Richland, WA; Karkamkar, Abhijeet J [Richland, WA; Zheng, Feng [Richland, WA

2011-03-01

The present invention discloses new methods for synthesizing ammonia borane (NH.sub.3BH.sub.3, or AB). Ammonium borohydride (NH.sub.4BH.sub.4) is formed from the reaction of borohydride salts and ammonium salts in liquid ammonia. Ammonium borohydride is decomposed in an ether-based solvent that yields AB at a near quantitative yield. The AB product shows promise as a chemical hydrogen storage material for fuel cell powered applications.

Nuclear hydrogen - possibilities for Brazil; Hidrogenio nuclear - possibilidades para o Brasil

Energy Technology Data Exchange (ETDEWEB)

Saliba-Silva, Adonis Marcelo; Linardi, Marcelo [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil). Centro de Celulas a Combustivel e Hidrogenio]. E-mail: saliba@ipen.br

2008-07-01

The energy vector hydrogen represents a good possibility to replace fossil fuels. One of the main renewable sources of interest for hydrogen is water, which is abundant and can be decomposed directly into pure H{sub 2} and O{sub 2}. This water splitting can be performed by the following methods: electrolysis, thermal decomposition, and thermochemical cycles. The thermochemical cycles and high temperature electrolysis (HTE) are often thought to be feasible methods to be associated with a High Temperature Gas cooled Reactor (HTGR). Both routines have high efficiency at temperature range of 700-950 deg C. In this work, is presented an attainable proposal for Brazilian production of hydrogen based on a HTGR followed by HTE system. A research group at Fuel Cell and Hydrogen Center - CCCH at IPEN/CNEN-SP has elaborated a working plan for 10 years, where it is proposed a R and D line for hydrogen production based on nuclear energy supplied by HTGR. So, in this work, a Brazilian program for researching in this area is proposed inviting potential cooperation. (author)

Interaction of simple indium iodides with silver- and aluminium iodides

International Nuclear Information System (INIS)

Denisov, Yu.N.; Halova, N.S.; Fedorov, P.I.

1976-01-01

Fusibility diagrams of the systems InI-AlI 3 , InI-AgI, InI 2 -AgI, and InI 2 -AlI 3 have been studied. In the system InI-AlI 3 a compound InAlI 4 has been detected having a melting point 194 deg C and two lamination regions. In the system InI-AgI two compounds In 2 AgI 3 and InAgI 2 are formed which melt incongruently at 272 deg and 220 deg C, respectively. The formation of the compounds has been confirmed by X-ray phase analysis. Specific electroconductivity of a number of alloys of the system InI-AlI 3 has been studied. The systems of eutectic type formed by diiodide of indium with iodides of silver and aluminium have been studied by thermal and X-ray analysis and by measuring electroconductivity

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.

Mercuric Iodide Anticoincidence Shield for Gamma-Ray Spectrometer, Phase I

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...

Mercuric Iodide Anticoincidence Shield for Gamma-Ray Spectrometer, Phase II

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...

Grotthuss Transport of Iodide in EMIM/I3 Ionic Crystal.

Science.gov (United States)

McDaniel, Jesse G; Yethiraj, Arun

2018-01-11

Highly ionic environments can mediate unusual chemical reactions that would otherwise be considered impossible based on chemical intuition. For example, the formation of a chemical bond between two iodide anions to form a divalent polyiodide anion is seemingly prohibited due to Coulombic repulsion. Using ab initio molecular dynamics simulations, we show that in the 1-ethyl-3-methylimidazolium (EMIM)/I 3 ionic crystal, the reactive formation of divalent and even trivalent polyiodide anions occurs with extremely small energetic barriers, due to the electrostatic field of the ionic lattice. A practical consequence of this anomalous reactivity is that iodide anions are efficiently transported within the crystal through a "Grotthuss-exchange" mechanism involving bond-breaking and forming events. We characterize two distinct transport pathways, involving both I 4 2- and I 7 3- intermediates, with fast transport of iodide resulting from the release of an I - anion on the opposite side of the intermediate species from the initial bond formation. The ordered cation arrangement in the crystal provides the necessary electrostatic screening for close approach of anions, suggesting a new counterintuitive approach to obtain high ionic conductivity. This new design principle could be used to develop better solid-state electrolytes for batteries, fuel cells, and supercapacitors.

Atomic-batched tensor decomposed two-electron repulsion integrals

Science.gov (United States)

Schmitz, Gunnar; Madsen, Niels Kristian; Christiansen, Ove

2017-04-01

We present a new integral format for 4-index electron repulsion integrals, in which several strategies like the Resolution-of-the-Identity (RI) approximation and other more general tensor-decomposition techniques are combined with an atomic batching scheme. The 3-index RI integral tensor is divided into sub-tensors defined by atom pairs on which we perform an accelerated decomposition to the canonical product (CP) format. In a first step, the RI integrals are decomposed to a high-rank CP-like format by repeated singular value decompositions followed by a rank reduction, which uses a Tucker decomposition as an intermediate step to lower the prefactor of the algorithm. After decomposing the RI sub-tensors (within the Coulomb metric), they can be reassembled to the full decomposed tensor (RC approach) or the atomic batched format can be maintained (ABC approach). In the first case, the integrals are very similar to the well-known tensor hypercontraction integral format, which gained some attraction in recent years since it allows for quartic scaling implementations of MP2 and some coupled cluster methods. On the MP2 level, the RC and ABC approaches are compared concerning efficiency and storage requirements. Furthermore, the overall accuracy of this approach is assessed. Initial test calculations show a good accuracy and that it is not limited to small systems.

Sorption of microamount of colloidal silver iodide on hydrated iron(III) oxide

International Nuclear Information System (INIS)

Kepak, F.; Nova, J.

1975-01-01

Sorption of a microamount of colloidal silver iodide labelled with 131 I on hydrated iron/III/ oxide suspension was studied. The sorption dependence upon pH, sorbent amount, and inert electrolyte concentration has revealed that sorption of silver iodide reaches no more than 63%. The sorption lasted one hour during which the maximum value was reached. Desorption time was one hour, as well. Except for measuring the sorption dependence on pH, the sorption pH was 7.0, temperature 24+-2 0 C. (F.G.)

A (de)composable theory of rhythm perception

NARCIS (Netherlands)

Desain, P.

1992-01-01

A definition is given of expectancy of events projected into the future by a complex temporal sequence. The definition can be decomposed into basic expectancy components projected by each time interval implicit in the sequence. A preliminary formulation of these basic curves is proposed and the

Potassium iodide stockpiling

International Nuclear Information System (INIS)

Krimm, R.W.

1983-01-01

After examination by the Federal Emergency Management Agency (FEMA) and other federal agencies of federal policy on the use and distribution of potassium iodide (KI) as a thyroid-blocking agent for use in off-site preparedness around commercial nuclear powerplants, FEMA believes the present shelf life of KI is too short, that the minimum ordering quantities are an obstacle to efficient procurement, and that the packaging format offered by the drug industry does not meet the wishes of state and local government officials. FEMA has asked assistance from the Food and Drug Administration in making it possible for those states wishing to satisfy appropriate requirements to do so at the minimum cost to the public. Given an appropriate packaging and drug form, there appears to be no reason for the federal government to have further involvement in the stockpiling of KI

Detection of apoptotic cells using propidium iodide staining

NARCIS (Netherlands)

Newbold, Andrea; Martin, Ben P.; Cullinane, Carleen; Bots, Michael

2014-01-01

Flow cytometry assays are often used to detect apoptotic cells in in vitro cultures. Depending on the experimental model, these assays can also be useful in evaluating apoptosis in vivo. In this protocol, we describe a propidium iodide (PI) flow cytometry assay to evaluate B-cell lymphomas that have

JAEA’s R&D on the Thermochemical Hydrogen Production IS Process

International Nuclear Information System (INIS)

Kasahara, Seiji; Tanaka, Nobuyuki; Noguchi, Hiroki; Iwatsuki, Jin; Takegami, Hiroaki; Yan, Xing L.; Kubo, Shinji

2014-01-01

Japan Atomic Energy Agency (JAEA) has studied iodine-sulfur (IS) process, a thermochemical cycle to produce hydrogen by water splitting. This process is a candidate application of high temperature heat from high temperature gas-cooled reactors. This paper outlines the IS process study in JAEA, in particular recent situation of the R&D. Reactor components and a total process facility are tested to evaluate their integrity. A Bunsen reactor, a H_2SO_4 decomposer and a HI decomposer made of industrial materials such as SiC ceramic, fluoroplastic and lining materials have been examined separately as reactor components. A semibatch test and a thermal cycle test were operated in the Bunsen reactor. H_2SO_4 decomposition test is in a bayonet type reactor and HI decomposition test in an adiabatic radial flow type reactor are now under way. On the basis of a demonstration of continuous hydrogen production of 31 NL/h by a glass apparatus, an experimental apparatus of the total IS process has just been constructed to verify integrity of process components of industrial materials, H_2 production scale of which is 200 NL/h. Electro-electrodialysis (EED) cells to concentrate HI before distillation and a SiC-made bayonet type H_2SO_4 decomposer are applied in the facility. Process data of EED cells has been collected aiming to improve H_2 production thermal efficiency. Influence of temperature, composition in solution and existence of impurities on the cell properties has been investigated. Reduction of heat input to a HI separation step by applying the results of the study was shown. (author)

Effects of Potassium Iodide on Low Avid Immunological Reactions ...

African Journals Online (AJOL)

In identical test conditions keeping appropriate control, the following ... Abstract. Background: Selective in‑vivo anti‑fungal action of potassium iodide (KI) is an enigma, but .... mechanism of action of the drug against selective infections. In fact, if ...

Alpha-lipoic acid induces sodium iodide symporter expression in TPC-1 thyroid cancer cell line

International Nuclear Information System (INIS)

Choi, Hyun-Jeung; Kim, Tae Yong; Ruiz-Llorente, Sergio; Jeon, Min Ji; Han, Ji Min; Kim, Won Gu; Shong, Young Kee; Kim, Won Bae

2012-01-01

Introduction: Patients with metastatic thyroid cancers that do not uptake iodine need effective therapeutic option. Differentiation-inducing agents have been tried to restore functional expression of sodium iodide symporter (NIS) without success. Our objective was to assess the effect of alpha-lipoic acid (ALA), known as potential antioxidant, on expression of sodium iodide symporter in thyroid cancer cells. Methods: Human thyroid cancer-derived cell lines, TPC-1, were treated with ALA, and changes in NIS mRNA and protein expression were measured. ALA's effect on NIS gene promoter was evaluated, and functional NIS expression was assessed by iodide uptake assay. Results: Treatment with ALA increased NIS mRNA expression up to ten folds of control dose-dependently after 24 h of exposure. ALA increased NIS promoter activity, and increased iodide uptake by 1.6 fold. ALA induced expression of NIS protein, but had no significant effect on the plasma membrane trafficking. ALA increased phosphorylation of CREB and nuclear translocation of pCREB, and co-treatment of ALA and trichostatin A increased iodide uptake by three folds in TPC-1 cells. Conclusions: ALA is a potential agent to increase NIS transcription in TPC-1. It could be used as an adjunctive agent to increase efficacy of radioiodine therapy if combined with a strategy to increase NIS protein trafficking to cell membrane.

Small-molecule inhibitors of sodium iodide sym-porter function

International Nuclear Information System (INIS)

Lecat-Guillet, N.; Merer, G.; Lopez, R.; Rousseau, B.; Ambroise, Y.; Pourcher, T.

2008-01-01

The Na + /l - sym-porter (NIS) mediates iodide uptake into thyroid follicular cells. Although NIS has been cloned and thoroughly studied at the molecular level, the biochemical processes involved in post-translational regulation of NIS are still unknown. The purpose of this study was to identify and characterize inhibitors of NIS function. These small organic molecules represent a starting point in the identification of pharmacological tools for the characterization of NIS trafficking and activation mechanisms. screening of a collection of 17020 drug-like compounds revealed new chemical inhibitors with potencies down to 40 nM. Fluorescence measurement of membrane potential indicates that these inhibitors do not act by disrupting the sodium gradient. They allow immediate and total iodide discharge from preloaded cells in accord with a specific modification of NIS activity, probably through distinct mechanisms. (authors)

Small-molecule inhibitors of sodium iodide sym-porter function

Energy Technology Data Exchange (ETDEWEB)

Lecat-Guillet, N.; Merer, G.; Lopez, R.; Rousseau, B.; Ambroise, Y. [CEA, DSV, Dept Bioorgan Chem et Isotop Labelling, Inst Biol et Biotechnol iBiTecS, F-91191 Gif Sur Yvette (France); Pourcher, T. [Univ Nice Sophia Antipolis, Dept Biochem et Nucl Toxicol, F-06107 Nice (France)

2008-07-01

The Na{sup +}/l{sup -} sym-porter (NIS) mediates iodide uptake into thyroid follicular cells. Although NIS has been cloned and thoroughly studied at the molecular level, the biochemical processes involved in post-translational regulation of NIS are still unknown. The purpose of this study was to identify and characterize inhibitors of NIS function. These small organic molecules represent a starting point in the identification of pharmacological tools for the characterization of NIS trafficking and activation mechanisms. screening of a collection of 17020 drug-like compounds revealed new chemical inhibitors with potencies down to 40 nM. Fluorescence measurement of membrane potential indicates that these inhibitors do not act by disrupting the sodium gradient. They allow immediate and total iodide discharge from preloaded cells in accord with a specific modification of NIS activity, probably through distinct mechanisms. (authors)

α-, β-, and δ-Hydrogen Abstraction in the Thermolysis of Paramagnetic Vanadium(III) Dialkyl Complexes

NARCIS (Netherlands)

Hessen, Bart; Buijink, Jan-Karel F.; Meetsma, Auke; Teuben, Jan H.; Helgesson, Göran; Håkansson, Mikael; Jagner, Susan; Spek, Anthony L.

1993-01-01

Electron deficient paramagnetic vanadium(III) diakyls CpV(CH2CMe2R)2(PMe3) (14 electron, R = Me (2), Ph (3)) and CpV[CH(SiMe3)2]2 (12 electron, 4) have been synthesized. At ambient temperature 2 decomposes through α-hydrogen abstraction to produce, in the presence of dmpe

Decomposed process mining with DivideAndConquer

NARCIS (Netherlands)

Verbeek, H.M.W.; Limonad, L.; Weber, B.

2014-01-01

Many known process mining techniques scale badly in the number of activities in an event log. Examples of such techniques include the ILP Miner and the standard replay, which also uses ILP techniques. To alleviate the problems these techniques face, we can decompose a large problem (with many

A general approach to decomposable bi-capacities

Czech Academy of Sciences Publication Activity Database

Saminger, S.; Mesiar, Radko

2003-01-01

Roč. 39, č. 5 (2003), s. 631-642 ISSN 0023-5954 R&D Projects: GA ČR GA402/04/1026 Institutional research plan: CEZ:AV0Z1075907 Keywords : bi-capacity * cumulative prospect theory * decomposable capacity Subject RIV: BA - General Mathematics Impact factor: 0.319, year: 2003

Kinetic modeling of the purging of activated carbon after short term methyl iodide loading

International Nuclear Information System (INIS)

Friedrich, V.; Lux, I.

1991-01-01

A bimolecular reaction model containing the physico-chemical parameters of the adsorption and desorption was developed earlier to describe the kinetics of methyl iodide retention by activated carbon adsorber. Both theoretical model and experimental investigations postulated constant upstream methyl iodide concentration till the maximum break-through. The work reported here includes the extension of the theoretical model to the general case when the concentration of the challenging gas may change in time. The effect of short term loading followed by purging with air, and an impulse-like increase in upstream gas concentration has been simulated. The case of short term loading and subsequent purging has been experimentally studied to validate the model. The investigations were carried out on non-impregnated activated carbon. A 4 cm deep carbon bed had been challenged by methyl iodide for 30, 90, 120 and 180 min and then purged with air, downstream methyl iodide concentration had been measured continuously. The main characteristics of the observed downstream concentration curves (time and slope of break-through, time and amplitude of maximum values) showed acceptable agreement with those predicted by the model

Extraction method for the determination of inorganic iodides in Rose Bengal labelled with 131I

International Nuclear Information System (INIS)

Lengyel, J.; Krtil, J.; Vecernik, J.

1982-01-01

An extraction method for the determination of inorganic iodides in Rose Bengal preparations labelled with 131 I is described. The method is based on the quantitative extraction of Rose Bengal into chloroform from acidic medium while the inorganic iodides remain in the aqueous phase. The method is simple, rapid, and reproducible. (author)

GaN CVD Reactions: Hydrogen and Ammonia Decomposition and the Desorption of Gallium

International Nuclear Information System (INIS)

Bartram, Michael E.; Creighton, J. Randall

1999-01-01

Isotopic labeling experiments have revealed correlations between hydrogen reactions, Ga desorption, and ammonia decomposition in GaN CVD. Low energy electron diffraction (LEED) and temperature programmed desorption (TPD) were used to demonstrate that hydrogen atoms are available on the surface for reaction after exposing GaN(0001) to deuterium at elevated temperatures. Hydrogen reactions also lowered the temperature for Ga desorption significantly. Ammonia did not decompose on the surface before hydrogen exposure. However, after hydrogen reactions altered the surface, N 15 H 3 did undergo both reversible and irreversible decomposition. This also resulted in the desorption of N 2 of mixed isotopes below the onset of GaN sublimation, This suggests that the driving force of the high nitrogen-nitrogen bond strength (226 kcal/mol) can lead to the removal of nitrogen from the substrate when the surface is nitrogen rich. Overall, these findings indicate that hydrogen can influence G-aN CVD significantly, being a common factor in the reactivity of the surface, the desorption of Ga, and the decomposition of ammonia

Uptake of Iodide From Water in Atlantic Halibut Larvae (Hippoglossus Hippoglossus L.)

DEFF Research Database (Denmark)

Moren, Mari; Sloth, Jens Jørgen; Hamre, Kristin

2008-01-01

The natural diet of marine fish larvae, copepods, contain 60-350 mg I kg(-1), while live feed used in commercial hatcheries have iodine concentrations in the range of 1 mg kg(-1). Seawater is also considered to be an important source of iodine for marine fish. The question asked in this study is ......M. The uptake was partly blocked by perchlorate (ClO3-) which is a known inhibitor of the sodium iodide symporter. This indicates that the Atlantic halibut larvae accumulate iodide through both specific and non-specific uptake pathways....

Method for removing radioactive iodine and radioactive organic iodides from effluent gases

International Nuclear Information System (INIS)

1975-01-01

A method and composition for removing radioactive and organic iodides from an 131 I-containing off-gas stream is provided. The composition for removal by adsorption is a ceramic material with a surface area of from about 5 m 2 /g to about 250 m 2 /g impregnated with a metallic salt. The method for removing the iodine or iodide is accomplished by passing the off-gas stream over the ceramic material impregnated with the metallic salt. It finds special application in air filters for nuclear power plants

Iodine from bacterial iodide oxidization by Roseovarius spp. inhibits the growth of other bacteria.

Science.gov (United States)

Zhao, Dan; Lim, Choon-Ping; Miyanaga, Kazuhiko; Tanji, Yasunori

2013-03-01

Microbial activities in brine, seawater, or estuarine mud are involved in iodine cycle. To investigate the effects of the microbiologically induced iodine on other bacteria in the environment, a total of 13 bacteria that potentially participated in the iodide-oxidizing process were isolated from water or biofilm at a location containing 131 μg ml(-1) iodide. Three distinct strains were further identified as Roseovarius spp. based on 16 S rRNA gene sequences after being distinguished by restriction fragment length polymorphism analysis. Morphological characteristics of these three Roseovarius spp. varied considerably across and within strains. Iodine production increased with Roseovarius spp. growth when cultured in Marine Broth with 200 μg ml(-1) iodide (I(-)). When 10(6) CFU/ml Escherichia coli, Pseudomonas aeruginosa, and Bacillus pumilus were exposed to various concentrations of molecular iodine (I(2)), the minimum inhibitory concentrations (MICs) were 0.5, 1.0, and 1.0 μg ml(-1), respectively. However, fivefold increases in the MICs for Roseovarius spp. were obtained. In co-cultured Roseovarius sp. IOB-7 and E. coli in Marine Broth containing iodide (I(-)), the molecular iodine concentration was estimated to be 0.76 μg ml(-1) after 24 h and less than 50 % of E. coli was viable compared to that co-cultured without iodide. The growth inhibition of E. coli was also observed in co-cultures with the two other Roseovarius spp. strains when the molecular iodine concentration was assumed to be 0.52 μg ml(-1).

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

Fast iodide-SAD phasing for high-throughput membrane protein structure determination.

Science.gov (United States)

Melnikov, Igor; Polovinkin, Vitaly; Kovalev, Kirill; Gushchin, Ivan; Shevtsov, Mikhail; Shevchenko, Vitaly; Mishin, Alexey; Alekseev, Alexey; Rodriguez-Valera, Francisco; Borshchevskiy, Valentin; Cherezov, Vadim; Leonard, Gordon A; Gordeliy, Valentin; Popov, Alexander

2017-05-01

We describe a fast, easy, and potentially universal method for the de novo solution of the crystal structures of membrane proteins via iodide-single-wavelength anomalous diffraction (I-SAD). The potential universality of the method is based on a common feature of membrane proteins-the availability at the hydrophobic-hydrophilic interface of positively charged amino acid residues with which iodide strongly interacts. We demonstrate the solution using I-SAD of four crystal structures representing different classes of membrane proteins, including a human G protein-coupled receptor (GPCR), and we show that I-SAD can be applied using data collection strategies based on either standard or serial x-ray crystallography techniques.

The synergistic inhibitive effect and some quantum chemical parameters of 2,3-diaminonaphthalene and iodide ions on the hydrochloric acid corrosion of aluminium

International Nuclear Information System (INIS)

Obot, I.B.; Obi-Egbedi, N.O.; Umoren, S.A.

2009-01-01

The effect of iodide ions on the inhibitive performance of 2,3-diaminonaphthalene (2,3-DAN) in 1 M HCl for aluminium corrosion has been studied using hydrogen evolution (gasometry) measurements at 30 and 40 deg. C. Results obtained showed that the presence of 2,3-DAN molecules in the corrosive medium (1 M HCl solution) inhibits the corrosion process of aluminium and as the concentration of 2,3-DAN increases the inhibition efficiency also increased at the studied temperatures. A synergistic effect was observed between KI and 2,3-DAN. The experimental results suggest that the presence of iodide ions in the solutions stabilized the adsorption of 2,3-DAN molecules on the metal surfaces and, therefore improve the inhibition efficiency of 2,3-DAN. Phenomenon of physical adsorption is proposed for the inhibition and the process followed the Freundlich adsorption isotherm. The activation energy (E a ), heat of adsorption (Q ads ) and free energy of adsorption for the corrosion process (ΔG ads ) have been evaluated at the different temperatures and the values support the results obtained. Some quantum chemical parameters and the Mulliken charge densities for 2,3-diaminonaphthalene were calculated by the AM1 Semi-empirical method to provide further insight into the mechanism of inhibition of the corrosion process

Decarbonylation and hydrogenation reactions of allyl alcohol and acrolein on Pd(110)

Science.gov (United States)

Shekhar, Ratna; Barteau, Mark A.

1994-11-01

Allyl alcohol and acrolein reactions on the Pd(110) surface were investigated using temperature programmed desorption. For both unsaturated oxygenates, three coverage-dependent reaction pathways were observed. At low coverages, allyl alcohol decomposed completely to CO, hydrogen and carbonaceous species on the surface. For θ > 0.15 monolayer, ethylene (and small amounts of ethane) desorbed at ca. 295 K. Near saturation coverages, desorption of propanal was detected at ca. 235 K. The parent molecule, allyl alcohol, desorbed only after exposures sufficient to saturate these channels. Acrolein decomposition spectra were similar to those observed for allyl alcohol decomposition on the clean surface. Additional experiments with allyl alcohol on hydrogen- and deuterium-precoveredPd(110) surfaces demonstrated increased hydrogenation of the C 2-hydrocarbon products along with hydrogenation of allyl alcohol to 1-propanol. However, in contrast to previous results for allyl alcohol on the Pd(111) surface, there was no evidence for C-O scission reactions of any C 3 oxygenate on Pd(110).

A novel decomposition technique of friable asbestos by CHClF2-decomposed acidic gas

International Nuclear Information System (INIS)

Yanagisawa, Kazumichi; Kozawa, Takahiro; Onda, Ayumu; Kanazawa, Masazumi; Shinohara, Junichi; Takanami, Tetsuro; Shiraishi, Masatsugu

2009-01-01

Asbestos was widely used in numerous materials and building products due to their desirable properties. It is, however, well known that asbestos inhalation causes health damage and its inexpensive decomposition technique is necessary to be developed for pollution prevention. We report here an innovative decomposition technique of friable asbestos by acidic gas (HF and HCl) generated from the decomposition of CHClF 2 by the reaction with superheated steam at 800 deg. C. Chrysotile-asbestos fibers were completely decomposed to sellaite and magnesium silicofluoride hexahydrate by the reaction with CHClF 2 -decomposed acidic gas at 150 deg. C for 30 min. At high temperatures beyond 400 deg. C, sellaite and hematite were detected in the decomposed product. In addition, crocidolite containing wastes and amosite containing wastes were decomposed at 500 deg. C and 600 deg. C for 30 min, respectively, by CHClF 2 -decomposed acidic gas. The observation of the reaction products by phase-contrast microscopy (PCM) and scanning electron microscopy (SEM) confirmed that the resulting products did not contain any asbestos

Methyl iodide tests on used adsorbents

International Nuclear Information System (INIS)

Kovach, J.L.

1993-01-01

This paper discusses the history of events leading to the current problems in radioiodine test conditions. These radioiodine tests are performed in the adsorbent media from both safety and non-safety related Nuclear Air Treatment Systems (NATS). The main problem addressed is that currently there are still numerous plant technical specifications for NATS which reference outdated test protocols for the surveillance testing of the radioactive methyl iodide performance of the adsorbents. Recommendations for correcting the test condition problems are presented. 7 refs

Adsorption behavior of calcined layered double hydroxides towards removal of iodide contaminants

International Nuclear Information System (INIS)

Lu Liang; He Jing; Wei Min; Evans, D.G.; Duan Xue

2005-01-01

Layered double hydroxides (LDHs), are a class of synthetic anionic clays whose structure can be described as containing brucite-like layers in which some of the divalent cations have been replaced by trivalent ions giving positively-charged sheets. This charge is balanced by intercalation of anions in the hydrated interlayer regions. The general formula is EM 2+ 1-x M 3+ x (OH) 2 ] x+ (A n- ) x/n · mH 2 O, where M 2+ and M 3+ are metal cations for example Mg 2+ and Al 3+ , that occupy octahedral sites in the hydroxide layers, A n- is an exchangeable anion, and x is the ratio M 3+ /(M 2+ + M 3+ ) and the layer charge will depend on the M 2+ /M 3+ ratio. LDHs act as sorbents of anionic species through two types of reactions, namely, anion exchange and reconstruction, which further adds the possibility of recycling and reuse. The sorption of anions from aqueous solutions by structural reconstruction of a calcined LDH is based on a very interesting property of these materials, the so-called memory effect: Calcination of LDHs produces intermediate non-stoichiometric oxides (CLDH) which undergo rehydration in aqueous medium and give back the hydroxide structure with different anions in the interlayers. Radioactive iodide is widely used in biological experiments, medical treatments and in diagnosis. During fission of uranium several iodine species are produced. All the short lived isotopes of iodine, including 1311 (half life 8.04 days), decay and only 127 I (stable) and 129 I (half life 1.59 x 10 7 years) remain as a problem. 129 I is especially considered as one of the key radionuclides that dominate the long-term radiation in underground radioactive waste stores. Iodine is one of the nuclides causing most concern among radioactive anions. Different adsorbents such as zeolites, silica gel, anion exchange paper membrane, activated carbon and activated carbon fibers, have been investigated as potential materials for elimination of iodide from liquid wastes. In this work

Impact of humic acid on the photoreductive degradation of perfluorooctane sulfonate (PFOS) by UV/Iodide process.

Science.gov (United States)

Sun, Zhuyu; Zhang, Chaojie; Chen, Pei; Zhou, Qi; Hoffmann, Michael R

2017-12-15

Iodide photolysis under UV illumination affords an effective method to produce hydrated electrons (e aq - ) in aqueous solution. Therefore, UV/Iodide photolysis can be utilized for the reductive degradation of many recalcitrant pollutants. However, the effect of naturally occurring organic matter (NOM) such as humic and fulvic acids (HA/FA), which may impact the efficiency of UV/Iodide photoreduction, is poorly understood. In this study, the UV photoreductive degradation of perfluorooctane sulfonate (PFOS) in the presence of I - and HA is studied. PFOS undergoes a relatively slow direct photoreduction in pure water, a moderate level of degradation via UV/Iodide, but a rapid degradation via UV/Iodide/HA photolysis. After 1.5 h of photolysis, 86.0% of the initial [PFOS] was degraded in the presence of both I - and HA with a corresponding defluorination ratio of 55.6%, whereas only 51.7% of PFOS was degraded with a defluorination ratio of 4.4% via UV/Iodide illumination in the absence of HA. The relative enhancement in the presence of HA in the photodegradation of PFOS can be attributed to several factors: a) HA enhances the effective generation of e aq - due to the reduction of I 2 , HOI, IO 3 - and I 3 - back to I - ; b) certain functional groups of HA (i.e., quinones) enhance the electron transfer efficiency as electron shuttles; c) a weakly-bonded association of I - and PFOS with HA increases the reaction probability; and d) absorption of UV photons by HA itself produces e aq - . The degradation and defluorination efficiency of PFOS by UV/Iodide/HA process is dependent on pH and HA concentration. As pH increases from 7.0 to 10.0, the enhancement effect of HA improves significantly. The optimal HA concentration for the degradation of 0.03 mM PFOS is 1.0 mg L -1 . Copyright © 2017 Elsevier Ltd. All rights reserved.

The sodium iodide symporter: its implications for imaging and therapy

International Nuclear Information System (INIS)

Spitzweg, C.

2007-01-01

The sodium iodide symporter (NIS) is an intrinsic plasma membrane glycoprotein that mediates the active transport of iodide in the thyroid gland and a number of extrathyroidal tissues, in particular lactating mammary gland. In addition to its key function in thyroid physiology, NIS-mediated iodide accumulation allows diagnostic thyroid scintigraphy as well as therapeutic radioiodine application in benign and malignant thyroid disease. NIS therefore represents one of the oldest targets for molecular imaging and therapy. Based on the effective administration of radioiodine that has been used for over 60 years in the management of follicular cell-derived thyroid cancer, cloning and characterization of the NIS gene has paved the way for the development of a novel cytoreductive gene therapy strategy based on targeted NIS expression in thyroidal and nonthyroidal cancer cells followed by therapeutic application of 131 I or alternative radionuclides, including 188 Re and 211 At. In addition, the possibility of direct and non-invasive imaging of functional NIS expression by 123 I- and 99m Tc-scintigraphy or 124 I-PET-imaging allows the application of NIS as a novel reporter gene. In conclusion, the dual role of NIS as diagnostic and therapeutic gene and the detection of extra-thyroidal endogenous NIS expression in breast cancer open promising perspectives in nuclear medicine and molecular oncology for diagnostic and therapeutic application of NIS outside the thyroid gland. (orig.)

Comparative evaluation of the bacteria isolated from decomposing ...

African Journals Online (AJOL)

Six (6) bacterial species Bacillus circulans, Bacillus pumilus, Bacillus subtilis, Micrococcus luteus, Streptococcus faecalis and Streptococcus lactis were isolated from decomposing cow milk, while four (4) bacterial species namely Bacillus brevis, Bacillus licheniformis, Lactobacillus casei and Staphylococcus epidermidis ...

Apparatus for eliminating radioactive iodine from off-gases in a nuclear fuel reprocessing plant

International Nuclear Information System (INIS)

Kondo, Yoshikazu; Kurihara, Koichi.

1983-01-01

Purpose: To improve the eliminating efficiency of an iodine eliminating apparatus using a dry process. Constitution: A hydrogen iodide conversion device and an organic iodine decomposing device are disposed prior to and subsequent to an adsorption tower using adsorbents for the removal of the iodine in a processing gas line through which radioactive iodine containing gases are passed. Elementary iodine and organic iodine can be eliminated by such simple devices. In the case of the dry processing by using the adsorbents, those adsorbents incorporated with inexpensive metal such as lead and copper can be used for the removal of the organic iodine and the radioactive iodine-adsorbing material can be processed as wastes, whereby iodine can effectively be eliminated at a reduced cost. (Moriyama, K.)

High Chloride Doping Levels Stabilize the Perovskite Phase of Cesium Lead Iodide.

Science.gov (United States)

Dastidar, Subham; Egger, David A; Tan, Liang Z; Cromer, Samuel B; Dillon, Andrew D; Liu, Shi; Kronik, Leeor; Rappe, Andrew M; Fafarman, Aaron T

2016-06-08

Cesium lead iodide possesses an excellent combination of band gap and absorption coefficient for photovoltaic applications in its perovskite phase. However, this is not its equilibrium structure under ambient conditions. In air, at ambient temperature it rapidly transforms to a nonfunctional, so-called yellow phase. Here we show that chloride doping, particularly at levels near the solubility limit for chloride in a cesium lead iodide host, provides a new approach to stabilizing the functional perovskite phase. In order to achieve high doping levels, we first co-deposit colloidal nanocrystals of pure cesium lead chloride and cesium lead iodide, thereby ensuring nanometer-scale mixing even at compositions that potentially exceed the bulk miscibility of the two phases. The resulting nanocrystal solid is subsequently fused into a polycrystalline thin film by chemically induced, room-temperature sintering. Spectroscopy and X-ray diffraction indicate that the chloride is further dispersed during sintering and a polycrystalline mixed phase is formed. Using density functional theory (DFT) methods in conjunction with nudged elastic band techniques, low-energy pathways for interstitial chlorine diffusion into a majority-iodide lattice were identified, consistent with the facile diffusion and fast halide exchange reactions observed. By comparison to DFT-calculated values (with the PBE exchange-correlation functional), the relative change in band gap and the lattice contraction are shown to be consistent with a Cl/I ratio of a few percent in the mixed phase. At these incorporation levels, the half-life of the functional perovskite phase in a humid atmosphere increases by more than an order of magnitude.

Ostwald ripening of decomposed phases in Cu-Ni-Cr alloys

International Nuclear Information System (INIS)

Hernandez-Santiago, Felipe; Lopez-Hirata, Victor; Dorantes-Rosales, Hector J.; Saucedo-Munoz, Maribel L.; Gonzalez-Velazquez, Jorge L.; Paniagua-Mercado, Ana Ma.

2008-01-01

A study of the coarsening process of the decomposed phases was carried out in the Cu-34 wt.% Ni-4 wt.% Cr and Cu-45 wt.% Ni-10 wt.% Cr alloys using transmission electron microscopy. As aging progressed, the morphology of the coherent decomposed Ni-rich phase changed from cuboids to platelets aligned in the Cu-rich matrix directions. Prolonged aging caused the loss of coherency between the decomposed phases and the morphology of the Ni-rich phase changed to ellipsoidal. The variation of mean radius of the coherent decomposed phases with aging time followed the modified LSW theory for thermally activated growth in ternary alloy systems. The linear variation of the density number of precipitates and matrix supersaturation with aging time, also confirmed that the coarsening process followed the modified LSW theory in both alloys. The coarsening rate was faster in the symmetrical Cu-45 wt.% Ni-10 wt.% Cr alloy due to its higher volume fraction of precipitates. The activation energy for thermally activated growth was determined to be about 182 and 102 kJ mol -1 in the Cu-34 wt.% Ni-4 wt.% Cr and Cu-45 wt.% Ni-10 wt.% Cr alloys, respectively. The lower energy for the former alloy seems to be related to an increase in the atomic diffusion process as the chromium content increases. The size distributions of precipitates in the Cu-Ni-Cr alloys were broader and more symmetric than that predicted by the modified LSW theory for ternary alloys

Laboratory Simulation of Rolling Contact Fatigue Cracks in Wind Turbine Bearings Using Hydrogen Infused 100Cr6 Bearing Steel

DEFF Research Database (Denmark)

Janakiraman, Shravan; West, Ole; Klit, Peder

Premature fatigue failure is observed in rolling element bearings used in wind turbine components. It is believed that decomposed hydrogen from the lubricant diffuses into the surface of the bearing inner ring making it susceptible to failure. An attempt is made to simulate the formation of these...

Performance of iodide vapour absorption in the venturi scrubber working in self-priming mode

International Nuclear Information System (INIS)

Zhou, Yanmin; Sun, Zhongning; Gu, Haifeng; Miao, Zhuang

2016-01-01

Highlights: • The absorption performance for iodide vapour was studied under different conditions. • A mathematical model was developed to describe the iodide absorption process. • The venturi scrubber can ensure absorption efficiiency and reduce pressure loss. - Abstract: The self-priming venturi scrubber is the key component of filtered containment venting systems for the removal of radioactive products during severe accidents in nuclear power plants. This paper is focused on the absorption performance of iodide vapour in the venturi scrubber, based on experiment and mathematical calculation. The results indicate that the absorption efficiency is closely related to solution flow rate, gas flow rate and temperature, but is not sensitive to iodide inlet concentration. When solution flow rate is low, the absorption efficiency increases rapidly with increasing the solution flow rate, and when the solution is excessive, the absorption efficiency remains around 99% stably; the influence of gas flow rate on absorption efficiency is mainly reflected in the variation of gas and liquid contacting time; when the solution flow rate is low, the increase of gas flow rate will led to an obvious decrease in absorption efficiency; temperature is not important when gas flow rate in constant but becomes effective for improving the absorption efficiency when gas velocity is constant. The proposed mathematical model can predict the iodide absorption process well in the range of experimental conditions. Especially, in the condition of lower gas flow rate and higher solution flow rate, the prediction accuracy is more satisfactory; however the accuracy of prediction will decrease at higher gas flow rates and lower solution flow rates because of neglecting the transverse exchange between gas and liquid phase.

The 11C-radioisotopic study of methanol conversion on V-MCM-41; the influence of methyl iodide on the transformation

International Nuclear Information System (INIS)

Sarkadi-Priboczki, E.; Szelecsenyi, F.; Kovacs, Z.; Solmaz, A.; Balci, S.; Dogu, T.

2007-01-01

Complete text of publication follows. The MCM-41 mesoporous material has Lewis and even Bronsted acid sites to produce dimethyl ether with some hydrocarbons, while over metal modified MCM-41 mostly formaldehyde and dimethoxy methane (i.e. methylal) or methyl formate are produced. In present experiments V incorporated basically mild acid sites of MCM-41 was prepared by low temperature direct synthesis. The V-MCM-41 has enough main active Lewis sites (by V-) to form formaldehyde and also light Bronsted acid sites to let the adsorbed formaldehyde eliminate and afterwards, with methanol, to form dimethoxy methane in nonoxidative environment. This V-MCM-41 has been tested by ethanol conversion in non-oxidative environments too and diethoxy methane as main product was detected. In present work the methanol conversion, as well as the methanol co-reaction with methyl iodide are studied from the same V-MCM-41 sample using 11 C-technique. The 11 C-labelled radioactive methanol has been already applied for determination of methanol conversion rates on Cu-modified MCM-41. The V-MCM-41 was prepared by direct hydrothermal synthesis method. The adsorption rate of 11 C-methanol and, after the reaction, the desorption rate of the remaining 11 C-derivatives on catalyst were continuously detected by gamma detectors. The derivatives were analyzed by radio-gas chromatography (gas chromatograph with FID coupled on-line with a radioactivity detector). Both dimethyl ether and hydrocarbon formation are also in slight degrees according to weak Lewis and Bronsted acidities. Since the conversion was carried out without added oxygen gas, only the frame oxygen can take part into catalysis. In presence of non-radioactive methyl iodide, the radioactive methanol is converted to radioactive methyl iodide on V-MCM-41. The radio-GC analysis confirmed that the iodide induced change of the reaction performance was reversible i.e. the radioactive methyl iodide was regenerated to non-radioactive methyl

Decomposability and convex structure of thermal processes

Science.gov (United States)

Mazurek, Paweł; Horodecki, Michał

2018-05-01

We present an example of a thermal process (TP) for a system of d energy levels, which cannot be performed without an instant access to the whole energy space. This TP is uniquely connected with a transition between some states of the system, that cannot be performed without access to the whole energy space even when approximate transitions are allowed. Pursuing the question about the decomposability of TPs into convex combinations of compositions of processes acting non-trivially on smaller subspaces, we investigate transitions within the subspace of states diagonal in the energy basis. For three level systems, we determine the set of extremal points of these operations, as well as the minimal set of operations needed to perform an arbitrary TP, and connect the set of TPs with thermomajorization criterion. We show that the structure of the set depends on temperature, which is associated with the fact that TPs cannot increase deterministically extractable work from a state—the conclusion that holds for arbitrary d level system. We also connect the decomposability problem with detailed balance symmetry of an extremal TPs.

Laser Spectroscopy on Ozone Destruction by SF6 Decomposed Products

OpenAIRE

北嶋, 巌; 村上, 和幸; 田中, 淳一; 岡井, 善四郎

2002-01-01

This paper reports on the identification of the SF6 decomposed products and the possibility of the ozone destruction by it. SF6 gas absorbs very strongly the 10.6μm P branch of C02 laser beam,so that the trace detection under ppb will be easily performed by the laser photo-acoustic method. We observed a new absorption spectra within the 9.6μm P branch resulted from the decomposed molecules after 2 hours 1 Hz-pulsed discharge of SF6 gas. As a resu1t ofthe gas chromatograph, it will be assumed ...

Relations between oxygen and hydrogen generated by radiolysis in the systems of a CANDU 600

International Nuclear Information System (INIS)

Romano, Christian; Chocron, Mauricio; Urrutia, Guillermo

1999-01-01

The water that constitutes the coolant of the primary heat transport system, the moderator and the liquid control zones, decomposed under radiation producing as stable products oxygen, hydrogen and hydrogen peroxide throughout a complex mechanisms of radiolysis that involves ions and free radicals. These compound formed in different proportions alters the chemical control established for each system which purpose is to minimize the corrosion of the structural materials. In the present paper have been presented results of the modelling of the mentioned processes and it has been found that in the absence of a vapor phase, a relatively low concentration of hydrogen added to the water would be sufficient to control the formation of oxygen and hydrogen peroxide. The last species however, would remain in relatively high values inside a coolant fuel channel in the reactor core. (author)

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.

Activity of bimetallic catalysts (Pt + Me)/A12030 in butane hydrogenolysis and benzene hydrogenation

International Nuclear Information System (INIS)

Zharkov, B.B.; Rubinov, A.Z.

1986-01-01

The authors evaluate the decomposing and hydrogenating activity of some Me/Al 2 0 3 0 and (Pt + Me)/Al 203 catalysis for the reactions of butane hydrogenolysis and conversion of benzene to cyclohexane. The temperature was 180-300 C for butane transformation and 150 C for benzene hydrogenation. During both reactions some initial decrease of catalytic activity which stabilized over 2-3 h was observed. The results show that roasting Re-containing reforming catalysts at fairly high temperatures (500-550 C) balances maximum hydrogenating and average splitting activities, thus guaranteeing high resistance to coke deposition while preserving the necessary selectivity. The decreased hydrogenating capacity of Ir/A1 2 0 3 0 and (Pt + Ir)/A1 23 0 catalysts after roasting at 500 C indicates insufficient thermal stability, which can be why renewing the initial activity of iridium containing forming catalysts by oxidating regeneration is difficult

Decomposing the sales promotion bump with store data

NARCIS (Netherlands)

van Heerde, H.J.; Leeflang, P.S.H.; Wittink, D.R.

2004-01-01

Sales promotions generate substantial short-term sales increases. To determine whether the sales promotion bump is truly beneficial from a managerial perspective, we propose a system of store-level regression models that decomposes the sales promotion bump into three parts: cross-brand effects

Development of Assessment Methodology of Chemical Behavior of Volatile Iodide under Severe Accident Conditions Using EPICUR Experiments

International Nuclear Information System (INIS)

Oh, Jae Yong; Yun, Jong Il; Kim, Do Sam; Han Chul

2011-01-01

Iodine is one of the most important fission products produced in nuclear power plants. Under severe accident condition, iodine exists as a variety of species in the containment such as aqueous iodide, gaseous iodide, iodide aerosol, etc. Following release of iodine from the reactor, mostly in the form of CsI aerosol, volatile iodine can be generated from the containment sump and release to the environment. Especially, volatile organic iodide can be produced from interaction between nonvolatile iodine and organic substances present in the containment. Volatile iodide could significantly influence the alienated residents surrounding the nuclear power plant. In particular, thyroid is vulnerable to radioiodine due to its high accumulation. Therefore, it is necessary for the Korea Institute of Nuclear Safety (KINS) to develop an evaluation model which can simulate iodine behavior in the containment following a severe accident. KINS also needs to make up its methodology for radiological consequence analysis, based on MELCOR-MACCS2 calculation, by coupling a simple iodine model which can conveniently deal with organic iodides. In the long term, such a model can contribute to develop an accident source term, which is one of urgent domestic needs. Our strategy for developing the model is as follows: 1. Review the existing methodologies, 2. Develop a simple stand-alone model, 3. Validate the model using ISTP-EPICUR (Experimental Program on Iodine Chemistry under Radiation) and OECD-BIP (Behavior of Iodine Project) experimental data. In this paper we present the context of development and validation of our model named RAIM (Radio-active iodine chemistry model)

Development of Assessment Methodology of Chemical Behavior of Volatile Iodide under Severe Accident Conditions Using EPICUR Experiments

Energy Technology Data Exchange (ETDEWEB)

Oh, Jae Yong; Yun, Jong Il [KAIST, Daejeon (Korea, Republic of); Kim, Do Sam; Han Chul [Korea Institue of Nuclear Safety, Daejeon (Korea, Republic of)

2011-05-15

Iodine is one of the most important fission products produced in nuclear power plants. Under severe accident condition, iodine exists as a variety of species in the containment such as aqueous iodide, gaseous iodide, iodide aerosol, etc. Following release of iodine from the reactor, mostly in the form of CsI aerosol, volatile iodine can be generated from the containment sump and release to the environment. Especially, volatile organic iodide can be produced from interaction between nonvolatile iodine and organic substances present in the containment. Volatile iodide could significantly influence the alienated residents surrounding the nuclear power plant. In particular, thyroid is vulnerable to radioiodine due to its high accumulation. Therefore, it is necessary for the Korea Institute of Nuclear Safety (KINS) to develop an evaluation model which can simulate iodine behavior in the containment following a severe accident. KINS also needs to make up its methodology for radiological consequence analysis, based on MELCOR-MACCS2 calculation, by coupling a simple iodine model which can conveniently deal with organic iodides. In the long term, such a model can contribute to develop an accident source term, which is one of urgent domestic needs. Our strategy for developing the model is as follows: 1. Review the existing methodologies, 2. Develop a simple stand-alone model, 3. Validate the model using ISTP-EPICUR (Experimental Program on Iodine Chemistry under Radiation) and OECD-BIP (Behavior of Iodine Project) experimental data. In this paper we present the context of development and validation of our model named RAIM (Radio-active iodine chemistry model)

Tandem on-line continuous separations for atomic spectroscopic indirect analysis: iodide determination by ICP-AES

International Nuclear Information System (INIS)

Garcia, A.M.; Sanchez Uria, J.E.; Sanz-Medel, A.; Quintero Ortega, M.C.; Bautista, J.C.

1992-01-01

A sensitive and selective indirect determination of iodide by inductively coupled plasma emission spectrometry (ICP-AES) based on the principle of tandem on-line continuous separations as an alternative means of introducing samples into plasmas is proposed. Iodide is continuously extracted as an ion-pair into xylene by mixing the sample with Hg(II) and dipyridil solutions. The organic phase (containing the analyte in [Hg(Dipy) 2 ]I 2 form) is on-line continuously mixed with NaBH 4 (in DMF) and acetic acid solutions. Mercury vapour continuously generated from this organic phase is separated in a classical U-type gas-liquid separation device. The system has been optimized for the continuous extraction of KI, for the direct generation of cold mercury vapour from xylene and for the final ICP-AES determination of mercury. The optimised method has been applied to the determination of iodide (detection limit 20 ng/ml of iodide) in table salt and in synthetic samples. Very good agreement between found and certified results was observed. The usefulness and convenience of such alternative sample chemical pretreatment/presentation to the ICP is thus demonstrated for indirect determinations to be carried out by atomic spectroscopy methods. (authors)

Production of hydrogen from by-products of food industries by rhodospirillaceae

Energy Technology Data Exchange (ETDEWEB)

Reh, U.

1983-11-01

The decomposition of organic substances from food-by-products as whey, beet sugar molasses, cane-sugar-molasses and potato-water by the Rhodospirillaceae Rp. capsulata, Rp. acidophila, Rm. vannielii, Rs. rubrum, and Rs. tenue to hydrogen and carbon dioxide were tested. In a pre-cultivation Lactobacillus bulgaricus converted the sugars of the by-products into lactic acid, which is easier in handling. Rs. rubrum was superior in producing hydrogen from this nutrient. It released from whey up to 56% of the substrate hydrogen, from beet sugar molasses 42%, from cane-sugar-molasses 89% and from potato-water 19%. Out-door-researches were made to evaluate the decrease of hydrogen yield under the influence of weather as well as day and night periods compared to the homogeneous conditions of the laboratory. From 200 m/sup 3/ whey, the daily output of a dairy, 4000 m/sup 3/ hydrogen corresponding to an energy equivalent of 1000 l fuel oil could be produced. To achieve this, 130 000 m/sup 2/ have to be covered with batch fermenters. These results show, that there is nearly no hope to decompose food by-products by Rhodospirillaceae in large scale technology, unless a new processing technology using a flow-fermenter and raising the hydrogen production significantly will be found.

Limited Effects of Variable-Retention Harvesting on Fungal Communities Decomposing Fine Roots in Coastal Temperate Rainforests.

Science.gov (United States)

Philpott, Timothy J; Barker, Jason S; Prescott, Cindy E; Grayston, Sue J

2018-02-01

Fine root litter is the principal source of carbon stored in forest soils and a dominant source of carbon for fungal decomposers. Differences in decomposer capacity between fungal species may be important determinants of fine-root decomposition rates. Variable-retention harvesting (VRH) provides refuge for ectomycorrhizal fungi, but its influence on fine-root decomposers is unknown, as are the effects of functional shifts in these fungal communities on carbon cycling. We compared fungal communities decomposing fine roots (in litter bags) under VRH, clear-cut, and uncut stands at two sites (6 and 13 years postharvest) and two decay stages (43 days and 1 year after burial) in Douglas fir forests in coastal British Columbia, Canada. Fungal species and guilds were identified from decomposed fine roots using high-throughput sequencing. Variable retention had short-term effects on β-diversity; harvest treatment modified the fungal community composition at the 6-year-postharvest site, but not at the 13-year-postharvest site. Ericoid and ectomycorrhizal guilds were not more abundant under VRH, but stand age significantly structured species composition. Guild composition varied by decay stage, with ruderal species later replaced by saprotrophs and ectomycorrhizae. Ectomycorrhizal abundance on decomposing fine roots may partially explain why fine roots typically decompose more slowly than surface litter. Our results indicate that stand age structures fine-root decomposers but that decay stage is more important in structuring the fungal community than shifts caused by harvesting. The rapid postharvest recovery of fungal communities decomposing fine roots suggests resiliency within this community, at least in these young regenerating stands in coastal British Columbia. IMPORTANCE Globally, fine roots are a dominant source of carbon in forest soils, yet the fungi that decompose this material and that drive the sequestration or respiration of this carbon remain largely

A highly sensitive PVC membrane iodide electrode based on complexes of mercury(II) as neutral carrier.

Science.gov (United States)

Chai, Y-Q; Yuan, R; Xu, L; Xu, W-J; Dai, J-Y; Jiang, F

2004-09-01

A novel solvent polymeric membrane electrode based on bis(1,3,4-thiadiazole) complexes of Hg(II) is described which has excellent selectivity and sensitivity toward iodide ion. The electrode, containing 1,4-bis(5-methyl-1,3,4-thiadiazole-2-yl-thio)butanemercury(II) [Hg(II)BMTB(NO3)4], has a Nernstian potentiometric response from 2.0 x 10(-8) to 2.0 x 10(-2) mol L(-1) with a detection limit of 8.0 x 10(-9) mol L(-1) and a slope of -59.0+/-0.5 mV/decade in 0.01 mol L(-1) phosphate buffer solution (pH 3.0, 20 degrees C). The selectivity sequence observed is iodide>bromide>thiocyanate>nitrite>nitrate>chloride>perchlorate>acetate>sulfate. The selectivity behavior is discussed in terms of the UV-Vis spectrum, and the process of transfer of iodide across the membrane interface is investigated by use of the AC impedance technique. The electrode was successfully applied to the determination of iodide in Jialing River and Spring in Jinyun Mountains, with satisfactory results.

Congenital Hypothyroidism Caused by a PAX8 Gene Mutation Manifested as Sodium/Iodide Symporter Gene Defect

Directory of Open Access Journals (Sweden)

Wakako Jo

2010-01-01

Full Text Available Loss-of-function mutations of the PAX8 gene are considered to mainly cause congenital hypothyroidism (CH due to thyroid hypoplasia. However, some patients with PAX8 mutation have demonstrated a normal-sized thyroid gland. Here we report a CH patient caused by a PAX8 mutation, which manifested as iodide transport defect (ITD. Hypothyroidism was detected by neonatal screening and L-thyroxine replacement was started immediately. Although 123I scintigraphy at 5 years of age showed that the thyroid gland was in the normal position and of small size, his iodide trapping was low. The ratio of the saliva/plasma radioactive iodide was low. He did not have goiter; however laboratory findings suggested that he had partial ITD. Gene analyses showed that the sodium/iodide symporter (NIS gene was normal; instead, a mutation in the PAX8 gene causing R31H substitution was identified. The present report demonstrates that individuals with defective PAX8 can have partial ITD, and thus genetic analysis is useful for differential diagnosis.

Diesel autothermal reforming with hydrogen peroxide for low-oxygen environments

International Nuclear Information System (INIS)

Han, Gwangwoo; Lee, Sangho; Bae, Joongmyeon

2015-01-01

Highlights: • The concept of diesel reforming using hydrogen peroxide was newly proposed. • Characteristics of hydrogen peroxide was experimentally investigated. • Thermodynamically possible operating conditions were analyzed. • Catalytic performance of Ni–Ru/CGO for various diesel compounds was evaluated. • Long-term testing was successfully conducted using Korean commercial diesel. - Abstract: To operate fuel cells effectively in low-oxygen environments, such as in submarines and unmanned underwater vehicles, a hydrogen source with high hydrogen storage density is required. In this paper, diesel autothermal reforming (ATR) with hydrogen peroxide as an alternative oxidant is proposed as a hydrogen production method. Diesel fuel has higher hydrogen density than metal hydrides or other hydrocarbons. In addition, hydrogen peroxide can decompose into steam and oxygen, which are required for diesel ATR. Moreover, both diesel fuel and hydrogen peroxide are liquid states, enabling easy storage for submarine applications. Hydrogen peroxide exhibited the same characteristics as steam and oxygen when used as an oxidant in diesel reforming when pre-decomposition method was used. The thermodynamically calculated operating conditions were a steam-to-carbon ratio (SCR) of 3.0, an oxygen-to-carbon ratio (OCR) of 0.5, and temperatures below 700 °C to account for safety issues associated with hydrogen peroxide use and exothermic reactions. Catalytic activity and stability tests over Ni–Ru (19.5–0.5 wt.%)/Ce 0.9 Gd 0.1 O 2−x were conducted using various diesel compounds. Furthermore, long-term diesel ATR tests were conducted for 200 h using Korean commercial diesel. The degradation rate was 3.67%/100 h without the production of ethylene

Comparison of two novel in-syringe dispersive liquid-liquid microextraction techniques for the determination of iodide in water samples using spectrophotometry.

Science.gov (United States)

Kaykhaii, Massoud; Sargazi, Mona

2014-01-01

Two new, rapid methodologies have been developed and applied successfully for the determination of trace levels of iodide in real water samples. Both techniques are based on a combination of in-syringe dispersive liquid-liquid microextraction (IS-DLLME) and micro-volume UV-Vis spectrophotometry. In the first technique, iodide is oxidized with nitrous acid to the colorless anion of ICl2(-) at high concentration of hydrochloric acid. Rhodamine B is added and by means of one step IS-DLLME, the ion-pair formed was extracted into toluene and measured spectrophotometrically. Acetone is used as dispersive solvent. The second method is based on the IS-DLLME microextraction of iodide as iodide/1, 10-phenanthroline-iron((II)) chelate cation ion-pair (colored) into nitrobenzene. Methanol was selected as dispersive solvent. Optimal conditions for iodide extraction were determined for both approaches. Methods are compared in terms of analytical parameters such as precision, accuracy, speed and limit of detection. Both methods were successfully applied to determining iodide in tap and river water samples. Copyright © 2013 Elsevier B.V. All rights reserved.

Hydrogen production by water dissociation using ceramic membranes - annual report for FY 2010.

Energy Technology Data Exchange (ETDEWEB)

Balachandran, U.; Dorris, S. E.; Emerson, J. E.; Lee, T. H.; Lu, Y.; Park, C. Y.; Picciolo, J. J. (Energy Systems)

2011-03-14

The objective of this project is to develop dense ceramic membranes that can produce hydrogen via coal/coal gas-assisted water dissociation without using an external power supply or circuitry. This project grew from an effort to develop a dense ceramic membrane for separating hydrogen from gas mixtures such as those generated during coal gasification, methane partial oxidation, and water-gas shift reactions. That effort led to the development of various cermet (i.e., ceramic/metal composite) membranes that enable hydrogen production by two methods. In one method, a hydrogen transport membrane (HTM) selectively removes hydrogen from a gas mixture by transporting it through either a mixed protonic/electronic conductor or a hydrogen transport metal. In the other method, an oxygen transport membrane (OTM) generates hydrogen mixed with steam by removing oxygen that is generated through water splitting. This project focuses on the development of OTMs that efficiently produce hydrogen via the dissociation of water. Supercritical boilers offer very high-pressure steam that can be decomposed to provide pure hydrogen using OTMs. Oxygen resulting from the dissociation of steam can be used for coal gasification, enriched combustion, or synthesis gas production. Hydrogen and sequestration-ready CO{sub 2} can be produced from coal and steam by using the membrane being developed in this project. Although hydrogen can also be generated by high-temperature steam electrolysis, producing hydrogen by water splitting with a mixed-conducting membrane requires no electric power or electrical circuitry.

Mechanochemical synthesis of nanostructured chemical hydrides in hydrogen alloying mills

International Nuclear Information System (INIS)

Wronski, Z.; Varin, R.A.; Chiu, C.; Czujko, T.; Calka, A.

2007-01-01

Mechanical alloying of magnesium metal powders with hydrogen in specialized hydrogen ball mills can be used as a direct route for mechanochemical synthesis of emerging chemical hydrides and hydride mixtures for advanced solid-state hydrogen storage. In the 2Mg-Fe system, we have successfully synthesized the ternary complex hydride Mg 2 FeH 6 in a mixture with nanometric Fe particles. The mixture of complex magnesium-iron hydride and nano-iron released 3-4 wt.%H 2 in a thermally programmed desorption experiment at the range 285-295 o C. Milling of the Mg-2Al powder mixture revealed a strong competition between formation of the Al(Mg) solid solution and the β-MgH 2 hydride. The former decomposes upon longer milling as the Mg atoms react with hydrogen to form the hydride phase, and drive the Al out of the solid solution. The mixture of magnesium dihydride and nano-aluminum released 2.1 wt.%H 2 in the temperature range 329-340 o C in the differential scanning calorimetry experiment. The formation of MgH 2 was suppressed in the Mg-B system; instead, a hydrogenated amorphous phase (Mg,B)H x , was formed in a mixture with nanometric MgB 2 . Annealing of the hydrogen-stabilized amorphous mixture produced crystalline MgB 2

76 FR 16770 - Petition To Suspend and Cancel All Registrations for the Soil Fumigant Iodomethane (Methyl Iodide...

Science.gov (United States)

2011-03-25

... ENVIRONMENTAL PROTECTION AGENCY [EPA-HQ-OPP-2010-0541; FRL-8841-7] Petition To Suspend and Cancel... Earthjustice requesting that all uses of iodomethane (methyl iodide) be suspended and cancelled. The Agency is... uses of iodomethane (methyl iodide) be suspended and cancelled. The Agency is posting this petition for...

Theoretical and experimental investigations on the behaviour of iodine during severe accidents: organic iodide, iodine/silver reaction, iodine/iron reaction. Pt. 4: organic iodide. Final report

International Nuclear Information System (INIS)

Hellmann, S.; Greger, G.U.; Funke, F.; Bleier, A.; Zeeh, W.

1995-11-01

Analysis of the consequences of severe accidents in nuclear power plants requires knowledge of the behaviour of radionuclides relevant from the radiological viewpoint. The role played by radioiodine is particularly important. In the current modelling of iodine behaviour the heterogeneous formation of organic iodide is not adequately taken into consideration owing to a lack of data or insufficient accuracy of data. This project is intended to eliminate some gaps in critical areas. This final report, part 4, describes the tests carried out in the two relevant areas - heterogeneous formation of organic coatings in the gas phase (containment atmosphere) - heterogeneous formation of organic iodide at organic coatings in aqueous phase (containment sump). Moreover, modelling suggestions how to include the resulting knowledge in the iodine accident behaviour code IMPAIR are given. (orig.) [de

Effect of radioiodine irradiation of thyroid gland in vitro with a dose of 4-5 Gy on iodide transport in thyrocytes

International Nuclear Information System (INIS)

Paster, Yi.P.

2000-01-01

We study the influence of ouabain on the basal and thyrotropin-stimulated iodide uptake in thyroid gland preliminarily irradiated by radioiodine (absorbed dose: 4-5 Gy) in vitro. Newborn pig thyroid tissue was incubated in a medium, containing 37 kBq/ml of 131-iodine (absorbed dose: 4-5 Gy), washed and achieved by collagenase dissociation. Thyrocytes were incubated with thyrotropin (100.0 mE/ml), ouabain (0.1 mol/l), and 125-iodide (0.4 kBq/ml). Then cells were washed, stored at 4 degree C for 60 days, and the 125-iodide uptake was assessed. Ouabain depressed both the basal and thyrotropin-stimulated iodide uptakes by thyrocytes in vitro. After preliminary radioiodine irradiation of the thyroid tissue (absorbed dose: 4-5 Gy), ouabain stimulated both the basal and thyrotropin-stimulated iodide uptakes by thyrocytes

Quantitative mass-spectrometric analysis of hydrogen helium isotope mixtures

International Nuclear Information System (INIS)

Langer, U.

1998-12-01

This work deals with the mass-spectrometric method for the quantitative analysis of hydrogen-helium-isotope mixtures, with special attention to fusion plasma diagnostics. The aim was to use the low-resolution mass spectrometry, a standard measuring method which is well established in science and industry. This task is solved by means of the vector mass spectrometry, where a mass spectrum is repeatedly measured, but with stepwise variation of the parameter settings of a quadruple mass spectrometer. In this way, interfering mass spectra can be decomposed and, moreover, it is possible to analyze underestimated mass spectra of complex hydrogen-helium-isotope mixtures. In this work experimental investigations are presented which show that there are different parameters which are suitable for the UMS-method. With an optimal choice of the parameter settings hydrogen-helium-isotope mixtures can be analyzed with an accuracy of 1-3 %. In practice, a low sensitivity for small helium concentration has to be noted. To cope with this task, a method for selective hydrogen pressure reduction has been developed. Experimental investigations and calculations show that small helium amounts (about 1 %) in a hydrogen atmosphere can be analyzed with an accuracy of 3 - 10 %. Finally, this work deals with the effects of the measuring and calibration error on the resulting error in spectrum decomposition. This aspect has been investigated both in general mass-spectrometric gas analysis and in the analysis of hydrogen-helium-mixtures by means of the vector mass spectrometry. (author)

Epidemiology of thyroid disorders and valuation of effects of iodide administration in the Sejny community (Poland) after Chernobyl accident

International Nuclear Information System (INIS)

Zimnicki, P.

1993-01-01

The epidemiology of thyroid disorders was studied and the effect of potassium iodide administration was evaluated in citizens of Sejny (Poland) community four years after Chernobyl accident. The endemic goiter was observed in this area. The elevated levels of anti-human thyroid membrane antibodies and anti-human thereoglobuline antibody were found in 5.5% of children that had undergone iodide administration after Chernobyl accident. It may result from iodide administration or from endemic goiter. (author). 127 refs, 9 figs, 16 tabs

Synthesis and antimicrobial activity of guanylhydrazones. Synthesis of 2-(2-methylthio-2-aminovinyl)-1-methylpyridinium iodides and 2-(2-methylthio-2-aminovinyl)-1-methylquinolinium iodides as potential radioprotective and anticancer agents

International Nuclear Information System (INIS)

Almassian, B.

1985-01-01

The finding of appreciable antileukemic activity in a series of 2-(2-methylthio-2-amino)vinyl-1-methylquinolinium iodides (Foye et al., 1980, 1983) suggested that greater basicity, as compared with the corresponding dithioacetic acids, was contributing to the increase in activity. The addition of a greater degree of basicity in the design of anticancer possibilities in this series was considered worth investigation, particularly in view of the activity of a series of bis(quanylhydrazones) synthesized at Lederle Laboratories. Accordingly, a series of guanylhydrazones of 4-pyridine-,2-pyridine- and 4-quinolinecarboxyaldehydes was synthesized for anticancer as well as antibacterial screening. Also, substitution of additional basic functions in the 2-(2-methylthio-2-amino) vinyl-1-methylquinolinium and pyridinium iodide series has been made. Appreciable antimicrobial activities have been found with both 2-pyridine and 4-quinolinealdehyde guanylhydrazones, as well as with 2-(2-methylthio-2-amino)vinyl-1-methyl-pyridinium iodides. The overall approach to the synthesis of potential anticancer agents in this project is thus to observe the effect of increasing basicity of these compounds on DNA binding and anticancer activity

Thermoeconomic analysis of a copper-chlorine thermochemical cycle for nuclear-based hydrogen production

International Nuclear Information System (INIS)

Orhan, Mehmet F.; Dincer, Ibrahim; Rosen, Marc A.

2010-01-01

Thermochemical water splitting with a copper-chlorine (Cu-Cl) cycle is a promising process that could be linked with nuclear reactors to decompose water into its constituents, oxygen and hydrogen, through intermediate copper and chlorine compounds. In this paper, a comprehensive exergoeconomic analysis of the Cu-Cl cycle is reported to evaluate the production costs as a function of the amount and quality of the energy used for hydrogen production, as well as the costs of the exergy losses and the exergoeconomic improvement potential of the equipment used in the process. An additional objective is to determine changes in the design parameters of the Cu-Cl cycle that improve the cost effectiveness of the overall system. (orig.)

Domain decomposed preconditioners with Krylov subspace methods as subdomain solvers

Energy Technology Data Exchange (ETDEWEB)

Pernice, M. [Univ. of Utah, Salt Lake City, UT (United States)

1994-12-31

Domain decomposed preconditioners for nonsymmetric partial differential equations typically require the solution of problems on the subdomains. Most implementations employ exact solvers to obtain these solutions. Consequently work and storage requirements for the subdomain problems grow rapidly with the size of the subdomain problems. Subdomain solves constitute the single largest computational cost of a domain decomposed preconditioner, and improving the efficiency of this phase of the computation will have a significant impact on the performance of the overall method. The small local memory available on the nodes of most message-passing multicomputers motivates consideration of the use of an iterative method for solving subdomain problems. For large-scale systems of equations that are derived from three-dimensional problems, memory considerations alone may dictate the need for using iterative methods for the subdomain problems. In addition to reduced storage requirements, use of an iterative solver on the subdomains allows flexibility in specifying the accuracy of the subdomain solutions. Substantial savings in solution time is possible if the quality of the domain decomposed preconditioner is not degraded too much by relaxing the accuracy of the subdomain solutions. While some work in this direction has been conducted for symmetric problems, similar studies for nonsymmetric problems appear not to have been pursued. This work represents a first step in this direction, and explores the effectiveness of performing subdomain solves using several transpose-free Krylov subspace methods, GMRES, transpose-free QMR, CGS, and a smoothed version of CGS. Depending on the difficulty of the subdomain problem and the convergence tolerance used, a reduction in solution time is possible in addition to the reduced memory requirements. The domain decomposed preconditioner is a Schur complement method in which the interface operators are approximated using interface probing.

Temperature Dependent Charge Carrier Dynamics in Formamidinium Lead Iodide Perovskite

NARCIS (Netherlands)

Gelvez Rueda, M.C.; Renaud, N.; Grozema, F.C.

2017-01-01

The fundamental opto-electronic properties of organic-inorganic hybrid perovskites are strongly affected by their structural parameters. These parameters are particularly critical in formamidinium lead iodide (FAPbI₃), in which its large structural disorder leads to a non-perovskite

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

The mass transfer dynamics of gaseous methyl-iodide adsorption by silver-exchanged sodium mordenite

International Nuclear Information System (INIS)

Jubin, R.T.

1994-12-01

The adsorption of methyl iodide onto hydrogen-reduced silver-exchange mordenite was studied. The removal of organic iodides from off-gas streams is an important step in controlling the release of radioactive iodine to the environment during the treatment of radioactive wastes or the processing of some irradiated materials. Nine well accepted mass transfer models were evaluated for their ability to adequately explain the observed CH 3 I uptake behavior onto the Ag-Z. Linear and multidimensional regression techniques were utilized in the estimation of the diffusion constants and other model parameters which then permitted the selection of an appropriate mass transfer model. To date, only bulk loading data exist for the adsorption of CH 3 I onto Ag-Z. Hence this is believed to be the first study to quantify the controlling mass transfer mechanisms of this process. It can be concluded from the analysis of the experimental data obtained by the single-pellet type experiments and for the process conditions used in this study that the overall mass transfer rate associated with the adsorption of CH 3 I onto Ag-Z is affected by both micropore and macropore diffusion. The macropore diffusion rate was significantly faster than the micropore diffusion, resulting in a two-step adsorption behavior which was adequately modeled by a bimodal pore distribution model. The micropore diffusivity was determined to be on the order of 2 x 10 -14 cm 2 /s. The system was also shown to be isothermal under all conditions of this study. Two other conclusions were also obtained. First, the gas film resistance to mass transfer for the 1/16 and 1/8-in.-diam Ag-Z pellets can be ignored under the conditions used in this study. Finally, it was shown that by decreasing the water vapor content of the feed gas, the chemical reaction rate appeared to become the initial rate-limiting factor for the mass transfer. 75 refs

Growth of mercuric iodide single crystals from dimethylsulfoxide

International Nuclear Information System (INIS)

Carlston, R.C.

1976-01-01

Dimethylsulfoxide is used as a solvent for the growth of red mercuric iodide (HgI 2 ) crystals for use in radiation detectors. The hygroscopic property of the solvent allows controlled amounts of water to enter into the solvent phase and diminish the large solubility of HgI 2 so that the precipitating solid collects as well-defined euhedral crystals which grow into a volume of several cc

Study of adsorption properties of impregnated charcoal for airborne iodine and methyl iodide

International Nuclear Information System (INIS)

Qi-dong, L.; Sui-yuang, H.

1985-01-01

The adsorption characteristics of airborne radioiodine and methyl iodide on impregnated charcoal were investigated. The activated charcoal tested was made from home-made oil-palm shells, and KI and TEDA were used as impregnants. A new technique was used to plot the dynamic partial adsorption isotherm at challenge concentrations (concentration range of iodine: 1-20 ppm v/v). Some adsorption properties of the impregnated charcoal were estimated with the dynamic partial adsorption isotherm. The dependences of the adsorption capacity and penetration behavior for airborne iodine and methyl iodide on the ambient conditions (temperature, relative humidity, and superficial velocity) were studied

Analysis of oxygen and hydrogen adsorption on Nb(100) surface by scanning tunneling microscopy

International Nuclear Information System (INIS)

An, Bai; Wen, Mao; Fukuyama, Seiji; Yokogawa, Kiyoshi; Ichimura, Shingo; Yoshimura, Masamichi

2006-01-01

The surface structure of Nb(100) under the condition of cleaning, oxidation and hydrogen adsorption is observed by STM (scanning tunneling microscopy). The results obtained are followings; (1) (3 x 1)-O→(4 x 1)-O→c(2 x 2)-O→clean(1 x 1)structure was observed by atom level, and these atomic models of structures and STM images were verified by the first-principles calculations, (2) when the clean(1 x 1) structure exposed to hydrogen, dissociative adsorption of hydrogen was observed and Nb hydride cluster formed on the surface at room temperature. It was heated at about 450 - 670 K in UHV, the cluster decomposed into hydrogen and (1 x 1) structure with linear defect was formed. The c(2 x 2)-O structure by oxygen adsorption transformed into (1 x 1)-H structure with OH and Nb hydride cluster under hydrogen gas at room temperature. When it was heated in UHV at 640 K, OH desorbed from the surface and (1 x 1) structure with linear defect was generated. The surface of (3 x 1)-O structure was not changed by hydrogen. (S.Y.)

Analysis of perchlorate, thiocyanate, nitrate and iodide in human amniotic fluid using ion chromatography and electrospray tandem mass spectrometry

International Nuclear Information System (INIS)

Blount, Benjamin C.; Valentin-Blasini, Liza

2006-01-01

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 18 O 4 - , S 13 CN - and 15 NO 3 - 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 μg/L), thiocyanate (<10-5860, 89 μg/L), nitrate (650-8900, 1620 μg/L) and iodide (1.7-170, 8.1 μg/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

Interruption with the Migration of Iodide by GR(CT)

International Nuclear Information System (INIS)

Min, J. H.; Lee, J. K.; Jeong, J. T.

2012-01-01

The purpose of this study is to understand the influence of green rust on the migration of iodide. GR(CT) would be major corrosion product of iron near the seawater or saline layer in underground. The GR(CT) may play an important role in the retardation of the iodide migration in a deep geological environment due to it's anionic exchange reaction. In underground radioactive waste repository, the corrosion of iron canisters would be proceed as follows; Fe(II) and/or Fe(III) dissolved from iron containers → Fe(II)(OH) 2 and/or Fe(III)(OH) 3 → Green rust → Lepidocrocite or Magnetite → Goetite etc. Generally, the green rust has known to exist in environments close to the Fe(Π)/Fe(ΠΙ) transition zone or between the oxidized layer and reduced layer in the underground. As anion exchanger and strong reducer, the green rusts can affect the migration of anions, reactions involving green rusts were poorly studied in relation to the safety assessment of radioactive waste repository

Iodine removal from a gas phase

International Nuclear Information System (INIS)

Vikis, A. Ch.

1982-01-01

Iodine, e.g. radioactive iodine, present as one or more organic iodides, optionally with elemental iodine, in a gas phase (e.g. air) are removed by photochemically decomposing the organic iodides to elemental iodine, reacting the iodine produced, and any initially present with excess ozone, preferably photochemically produced in situ in the gas phase to produce solid iodine oxides, and removing the solid oxides from the gas phase. (author)

Iodine removal from a gas phase

International Nuclear Information System (INIS)

Vikis, A.C.

1984-01-01

Iodine, e.g. radioactive iodine, present as one or more organic iodides, optionally with elemental iodine, in a gas phase (e.g. air) are removed by photochemically decomposing the organic iodides to elemental iodine, reacting the iodine produced, and any initially present with excess ozone, preferably photochemically produced in situ in the gas phase to produce solid iodine oxides, and removing the solid oxides from the gas phase

The distribution of radioiodine administrated to pregnant mice and the effect of non radioactive iodide

International Nuclear Information System (INIS)

Okui, Toyo; Kobayashi, Satoshi

1987-01-01

Radioiodine, 131 I, which has a high fission yield in the nuclear reactor, is easily taken into the human body, accumilating in the thyroid gland, when released to the environment. 131 I was administrated orally to pregnant mice, and its transportation to the tissues, particularly the fetus, was examined closely. And further, the non-radioactive iodide, i.e., KI, was administrated to see its radiation protection effect. The transportation of 131 I to the fetus is the second highest, following the thyroid gland in the mother mouse. This transportation to the fetus becomes the higher, the larger the gestation period at which the 131 I administration is made. The administration of the non-radioactive iodide has large radiation protection effect in the thyroid gland of the mother mouse and of the fetus. But, depending on its concentration, the non-radioactive iodide may conversely increase overall exposure of the fetus. (Mori, K.)

Functionalized metal organic frameworks for effective capture of radioactive organic iodides

KAUST Repository

Li, Baiyan; Dong, Xinglong; Wang, Hao; Ma, Dingxuan; Tan, Kui; Shi, Zhan; Chabal, Yves J.; Han, Yu; Li, Jing

2017-01-01

Highly efficient capture of radioactive organic iodides (ROIs) from off-gas mixtures remains a substantial challenge for nuclear waste treatment. Current materials utilized for ROI sequestration suffer from low capacity, high cost (e.g. use of noble

Studies on closed-cycle processes for hydrogen production, 3

International Nuclear Information System (INIS)

Sato, Shoichi; Ikezoe, Yasumasa; Shimizu, Saburo; Nakajima, Hayato; Kobayashi, Toshiaki

1978-10-01

Studies made in fiscal 1977 on the thermochemical and radiation chemical processes for hydrogen production are reported. In the thermochemical process, cerium (III) carbonate was used as an intermediate, and a workable process was found, which consisted of eight reaction steps. In other feasible processes, carbon dioxide was made to react with iron (II) chloride or iodide at high temperature to form carbon monoxide, and three or four reaction steps ensued. Also, an improved process of the sulfur cycle was studied. In this process, nickel salts were separated by solvent extraction. Estimated thermal efficiency (HHV) of the process was 30 - 40%, assuming 70 - 80% heat recovery. In the radiation chemical process, carbon dioxide was added with propane or nitrogen dioxide and radiolyzed: reaction mechanisms are discussed. (author)

Functional diversity of microbial decomposers facilitates plant coexistence in a plant-microbe-soil feedback model.

Science.gov (United States)

Miki, Takeshi; Ushio, Masayuki; Fukui, Shin; Kondoh, Michio

2010-08-10

Theory and empirical evidence suggest that plant-soil feedback (PSF) determines the structure of a plant community and nutrient cycling in terrestrial ecosystems. The plant community alters the nutrient pool size in soil by affecting litter decomposition processes, which in turn shapes the plant community, forming a PSF system. However, the role of microbial decomposers in PSF function is often overlooked, and it remains unclear whether decomposers reinforce or weaken litter-mediated plant control over nutrient cycling. Here, we present a theoretical model incorporating the functional diversity of both plants and microbial decomposers. Two fundamental microbial processes are included that control nutrient mineralization from plant litter: (i) assimilation of mineralized nutrient into the microbial biomass (microbial immobilization), and (ii) release of the microbial nutrients into the inorganic nutrient pool (net mineralization). With this model, we show that microbial diversity may act as a buffer that weakens plant control over the soil nutrient pool, reversing the sign of PSF from positive to negative and facilitating plant coexistence. This is explained by the decoupling of litter decomposability and nutrient pool size arising from a flexible change in the microbial community composition and decomposition processes in response to variations in plant litter decomposability. Our results suggest that the microbial community plays a central role in PSF function and the plant community structure. Furthermore, the results strongly imply that the plant-centered view of nutrient cycling should be changed to a plant-microbe-soil feedback system, by incorporating the community ecology of microbial decomposers and their functional diversity.

Optical power limiting and transmitting properties of cadmium iodide single crystals: Temperature dependence

Energy Technology Data Exchange (ETDEWEB)

Miah, M. Idrish, E-mail: m.miah@griffith.edu.a [Nanoscale Science and Technology Centre, Griffith University, Nathan, Brisbane, QLD 4111 (Australia)] [Biomolecular and Physical Sciences, Griffith University, Nathan, Brisbane, QLD 4111 (Australia)] [Department of Physics, University of Chittagong, Chittagong 4331 (Bangladesh)

2009-09-14

Optical limiting properties of the single crystals of cadmium iodide are investigated using ns laser pulses. It is found that the transmissions in the crystals increase with increasing temperature. However, they limit the transmissions at high input powers. The limiting power is found to be higher at higher temperature. From the measured transmission data, the photon absorption coefficients are estimated. The temperature dependence of the coefficients shows a decrease in magnitude with increasing temperature. This might be due to the temperature-dependent bandgap shift of the material. The results demonstrate that the cadmium iodide single crystals are promising materials for applications in optical power limiting devices.

Optical power limiting and transmitting properties of cadmium iodide single crystals: Temperature dependence

International Nuclear Information System (INIS)

Miah, M. Idrish

2009-01-01

Optical limiting properties of the single crystals of cadmium iodide are investigated using ns laser pulses. It is found that the transmissions in the crystals increase with increasing temperature. However, they limit the transmissions at high input powers. The limiting power is found to be higher at higher temperature. From the measured transmission data, the photon absorption coefficients are estimated. The temperature dependence of the coefficients shows a decrease in magnitude with increasing temperature. This might be due to the temperature-dependent bandgap shift of the material. The results demonstrate that the cadmium iodide single crystals are promising materials for applications in optical power limiting devices.

Methyl iodide retention on charcoal sorbents at parts-per-million concentrations

International Nuclear Information System (INIS)

Wood, G.O.; Vogt, G.J.; Kasunic, C.A.

1978-01-01

Breakthrough curves for charcoal beds challenged by air containing parts-per-million methyl iodide ( 127 I) vapor concentrations were obtained and analyzed. A goal of this research is to determine if sorbent tests at relatively high vapor concentrations give data that can be extrapolated many orders of magnitude to the region of interest for radioiodine retention and removal. Another objective is to identify and characterize parameters that are critical to the performance of a charcoal bed in a respirator cartridge application. Towards these ends, a sorbent test system was built that allows experimental variations of the parameters of challenge vapor concentration, volumetric flow rate, bed depth, bed diameter, and relative humidity. Methyl iodide breakthrough was measured at a limit of 0.002 ppM using a gas chromatograph equipped with a linearized electron capture detector. Several models that have been proposed to describe breakthrough curves were tested against experimental data. A variety of charcoals used or proposed for use in radioiodine air filtration systems have been tested against 25.7 ppM methyl iodide to obtain these parameters and protection (decomtamination) factors. Effects of challenge concentration, relative humidity, and bed diameter were also investigated. Significant challenge concentration dependence was measured (more efficiency at lower concentration) for two types of charcoals. Increased relative humidity greatly decreased breakthrough times for a given protection factor. Increased bed diameter greatly increased breakthrough times for a given protection factor. Implications of these effects for a test method are discussed

Method for ion exchange purification of sodium iodide solution from heavy metals and potassium microimpurities

International Nuclear Information System (INIS)

Smirnov, G.I.; Kachur, N.Ya.; Kostromina, O.N.; Ogorodnikova, A.A.; Khajnakov, S.A.

1990-01-01

A method of deep ion exchange purification of sodium iodide solution from heavy metals (iron, nickel, copper, lead) and potassium microimpurities is developed. The method includes multiple sorption of microimpurities on titanium phosphate with their subsequent desorption by sorbent processing with a solution with a solution of 3-6 N nitric acid, first, and then with a neutral solution of 2 % sodium thiosulfate. The given method permits to increase the purification degree of sodium iodide solution by 25-30 %. 2 tabs

H2-H2O-HI Hydrogen Separation in H2-H2O-HI Gaseous Mixture Using the Silica Membrane

International Nuclear Information System (INIS)

Pandiangan, Tumpal

2002-01-01

It was evaluated aiming at the application for hydrogen iodide decomposition in the thermochemical lS process. Porous alumina tube having pore size of 0.1 μm was modified by chemical vapor deposition using tetraethoxysilane. The permeance single gas of He, H 2 , and N 2 was measured at 300-600 o C. Hydrogen permeance of the modified membrane at a permeation temperature of 600 o C was about 5.22 x 10 -08 mol/Pa m 2 s, and 3.2 x 10 -09 of using gas mixture of H 2 -H 2 O-HI, where as HI permeances was below 1 x 10 -10 mol/Pa m 2 s. The Hydrogen permeance relative was not changed after 25 hours exposure in a mixture of H 2 -H 2 O-HI gas at the temperature of 450 o C. (author)

Silver-Assisted Synthesis of Gold Nanorods: the Relation between Silver Additive and Iodide Impurities.

Science.gov (United States)

Jessl, Sarah; Tebbe, Moritz; Guerrini, Luca; Fery, Andreas; Alvarez-Puebla, Ramon A; Pazos-Perez, Nicolas

2018-04-17

Seed-mediated methods employing cetyltrimethylammonium bromide (CTAB) as a surfactant, and silver salts as additives, are the most common synthetic strategies for high-yield productions of quality Au nanorods. However, the mechanism of these reactions is not yet fully understood and, importantly, significant lab-to-lab reproducibility issues still affect these protocols. In this study, the direct correlation between the hidden content of iodide impurities in CTAB reagents, which can drastically differ from different suppliers or batches, and the optimal concentration of silver required to maximize the nanorods yield is demonstrated. As a result, high-quality nanorods are obtained at different iodide contents. These results are interpreted based on the different concentrations of CTAB and cetyltrimethylammonium iodide (CTAI) complexes with Ag + and Au + metal ions in the growth solution, and their different binding affinity and reduction potential on distinct crystallographic planes. Notably, the exhaustive conversion of CTAI-Au + to CTAI-Ag + appears to be the key condition for maximizing the nanorod yield. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Impact of agricultural practices on selected soil decomposers fauna

International Nuclear Information System (INIS)

Abdalatif, M. A.; Alrayah, A.; Azar, W. Z.

2009-01-01

Soil decomposers fauna i.e. collembolan, mites and nematodes were studied and compared between and within sites in relation to site, treatment and time of collection in Shambat arable and El Rwakeeb dry land. Comparison of results between sites showed that population density/volume of decomposers fauna sampled from Shambat site exceeded their assemblages sampled from El Rawakeeb site. Treatment application in form of cattle manure and neem leaves powder were observed to induce insignificant changes in the three faunal groups between the two sites. Temporal variations showed significant annual variations and insignificant seasonal variations between the two sites. Within each site, population density/volume of each of collembolan, mites and nematodes increased in response to cattle manure application in both sites. Whereas, neem leaves powder application induced a significant decrease in population density/volume of collembola in both sites. These results are generally attributed to variability of soil properties which may add to the suitability of Shambat soil to El Rawakeeb one for the survival of decomposers fauna. Within each site, increase in population density/volume of these fauna upon cattle manure application was attributed to ability of cattle manure to improve soil properties and to provide food. The negative effect of neem leaves powder on mites and nematodes was attributed to neem toxicity, whereas, its positive effects on collembolan was attributed to the ability of collembolan to withstand neem toxicity, collembolan probably physiologically resistant and the neem powder provided food, thus increasing its numbers compared to the central treatment.(Author)

Decomposed Implicit Models of Piecewise - Linear Networks

Directory of Open Access Journals (Sweden)

J. Brzobohaty

1992-05-01

Full Text Available The general matrix form of the implicit description of a piecewise-linear (PWL network and the symbolic block diagram of the corresponding circuit model are proposed. Their decomposed forms enable us to determine quite separately the existence of the individual breakpoints of the resultant PWL characteristic and their coordinates using independent network parameters. For the two-diode and three-diode cases all the attainable types of the PWL characteristic are introduced.

Silver iodide reduction in aqueous solution: application to iodine enhanced separation during spent nuclear fuels reprocessing

International Nuclear Information System (INIS)

Badie, Jerome

2002-01-01

Silver iodide is a key-compound in nuclear chemistry either in accidental conditions or during the reprocessing of spent nuclear fuel. In that case, the major part of iodine is released in molecular form into the gaseous phase at the time of dissolution in nitric acid. In French reprocessing plants, iodine is trapped in the dissolver off-gas treatment unit by two successive steps: the first consists in absorption by scrubbing with a caustic soda solution and in the second, residual iodine is removed from the gaseous stream before the stack by chemisorption on mineral porous traps made up of beds of amorphous silica or alumina porous balls impregnated with silver nitrate. Reactions of iodine species with the impregnant are assumed to lead to silver iodide and silver iodate. Enhanced separation policy would make necessary to recover iodine from the filters by silver iodide dissolution during a reducing treatment. After a brief silver-iodine chemical bibliographic review, the possible reagents listed in the literature were studied. The choice has been made to use ascorbic acid and hydroxylamine. An experimental work on silver iodide reduction by this two compounds allowed us to determinate reaction products, stoichiometry and kinetics parameters. Finally, the process has been initiated on stable iodine loaded filters samples. (author) [fr

Towards a biochemical and structural characterisation of the sodium-iodide sym-porter (Nis)

International Nuclear Information System (INIS)

Darrouzet, E.; Marcellin, D.; Huc, S.; Quemeneur, E.; Pourcher, T.

2006-01-01

Iodide is essential for thyroid hormone biosynthesis in mammals, and therefore for the control of cell metabolism and the development of the central nervous system in the foetus and newborns, but is relatively scarce element in the environment. To ensure its accumulation, the thyroid gland has evolved a remarkably efficient system, the sodium-iodide sym-porter (NIS), that was first characterized at the molecular level 10 years ago (1). NIS is an intrinsic protein mainly located in the basolateral membrane of thyroid follicular cells where it actively transports iodide ions using the sodium gradient as a driving force (2,3). In addition, this transporter has been found in lactating mammary gland, stomach, and salivary glands, and its mRNA was detected in brain, ovaries, testis. To date, the physiological role of NIS in these organs is not yet identified (3,4).The capacity of NIS to mediate the accumulation of radioactive iodide has been exploited for many years in the diagnosis of thyroid cancer as well as for the detection and radiotherapy of derived metastases. Moreover, the presence of NIS in some breast tumours and the possibility to express it by targeted gene therapy in tumour cells where it is not naturally present could also widen its medical application (4-7). In case of accidental contamination, NIS would also be responsible for accumulation of radioisotopes in the thyroid and for their transfer to the milk and the newborn, eventually causing thyroid cancers. This has motivated our research program in the perspective of designing novel specific therapeutics. During the last decade, the gene encoding the thyroid NIS has been identified and sequenced in various species including rat, mouse and human (1, 8). It was also demonstrated that the protein expression and activity are highly regulated both at the transcriptional and post-translational levels (3). A preliminary topological mode could be drawn from the protein sequence. It proposes a general

1-(3-Iodopropyl-4-methylquinolin-1-ium Iodide

Directory of Open Access Journals (Sweden)

Todor Deligeorgiev

2015-11-01

Full Text Available A solvent-free “one-pot” synthetic approach to 1-(3-iodopropyl-4-methylquinolin-1-ium iodide is reported in the present work. The title compound is derived from N-alkylation of 4-methylquinoline with 1,3-diiodopropane proceeded at room temperature. The target quinolinium salt is obtained in a highly pure form. It’s structure was evaluated by 1H-NMR, 13C-NMR, and DEPT135 spectra.

Determination of Trace Anions in Concentrated Hydrogen Peroxide by Direct Injection Ion Chromatography with Conductivity Detection after Pt-Catalyzed On-Line Decomposition

International Nuclear Information System (INIS)

Kim, Do Hee; Lee, Bo Kyung; Lee, Dong Soo

1999-01-01

A method has been developed for the determination of trace anion impurities in concentrated hydrogen peroxide. The method involves on-line decomposition of hydrogen peroxide, ion chromatographic separation and subsequent suppressed-type conductivity detection. H 2 O 2 is decomposed in Pt-catalyst filled Gore-Tex membrane tubing and the resulting aqueous solution containing analytes is introduced to the injection valve of an ion chromatograph for periodic determinations. The oxygen gas evolving within the membrane tubing escapes freely through the membrane wall causing no problem in ion chromatographic analysis. Decomposition efficiency is above 99.99% at a flow rate of 0.4mL/min for a 30% hydrogen peroxide concentration. Analytes are quantitatively retained. The analysis results for several brands of commercial hydrogen peroxides are reported

Expedient Method for Samarium(II) Iodide Preparation Utilizing a Flow Approach

Czech Academy of Sciences Publication Activity Database

Voltrová, Svatava; Šrogl, Jiří

2013-01-01

Roč. 24, č. 3 (2013), s. 394-396 ISSN 0936-5214 R&D Projects: GA MŠk LH12013 Institutional support: RVO:61388963 Keywords : flow * samarium * iodide * reduction Subject RIV: CC - Organic Chemistry Impact factor: 2.463, year: 2013

Evaluation of perturbations in serum thyroid hormones during human pregnancy due to dietary iodide and perchlorate exposure using a biologically based dose-response model.

Science.gov (United States)

Lumen, Annie; Mattie, David R; Fisher, Jeffrey W

2013-06-01

A biologically based dose-response model (BBDR) for the hypothalamic pituitary thyroid (HPT) axis was developed in the near-term pregnant mother and fetus. This model was calibrated to predict serum levels of iodide, total thyroxine (T4), free thyroxine (fT4), and total triiodothyronine (T3) in the mother and fetus for a range of dietary iodide intake. The model was extended to describe perchlorate, an environmental and food contaminant, that competes with the sodium iodide symporter protein for thyroidal uptake of iodide. Using this mode-of-action framework, simulations were performed to determine the daily ingestion rates of perchlorate that would be associated with hypothyroxinemia or onset of hypothyroidism for varying iodide intake. Model simulations suggested that a maternal iodide intake of 75 to 250 µg/day and an environmentally relevant exposure of perchlorate (~0.1 µg/kg/day) did not result in hypothyroxinemia or hypothyroidism. For a daily iodide-sufficient intake of 200 µg/day, the dose of perchlorate required to reduce maternal fT4 levels to a hypothyroxinemic state was estimated at 32.2 µg/kg/day. As iodide intake was lowered to 75 µg/day, the model simulated daily perchlorate dose required to cause hypothyroxinemia was reduced by eightfold. Similarly, the perchlorate intake rates associated with the onset of subclinical hypothyroidism ranged from 54.8 to 21.5 µg/kg/day for daily iodide intake of 250-75 µg/day. This BBDR-HPT axis model for pregnancy provides an example of a novel public health assessment tool that may be expanded to address other endocrine-active chemicals found in food and the environment.

Role of endoplasmic reticulum stress-induced apoptosis in rat thyroid toxicity caused by excess fluoride and/or iodide.

Science.gov (United States)

Liu, Hongliang; Hou, Changchun; Zeng, Qiang; Zhao, Liang; Cui, Yushan; Yu, Linyu; Wang, Lingzhi; Zhao, Yang; Nie, Junyan; Zhang, Bin; Wang, Aiguo

2016-09-01

Excess fluoride and iodide coexist in drinking water in many regions, but few studies have investigated the single or interactive effects on thyroid in vivo. In our study, Wistar rats were exposed to excess fluoride and/or iodide through drinking water for 2 or 8 months. The structure and function of the thyroid, cells apoptosis and the expression of inositol-requiring enzyme 1 (IRE1) pathway-related factors were analyzed. Results demonstrated that excess fluoride and/or iodide could change thyroid follicular morphology and alter thyroid hormone levels in rats. After 8 months treatment, both single and co-exposure of the two microelements could raise the thyroid cells apoptosis. However, the expressions of IRE1-related factors were only increased in fluoride-alone and the combined groups. In conclusion, thyroid structure and thyroid function were both affected by excess fluoride and/or iodide. IRE1-induced apoptosis were involved in this cytotoxic process caused by fluoride or the combination of two microelements. Copyright © 2016 Elsevier B.V. All rights reserved.

New colorimetric and fluorometric sensing strategy based on the anisotropic growth of histidine-mediated synthesis of gold nanoclusters for iodide-specific detection.

Science.gov (United States)

Wang, Yifeng; Zhu, Haiyan; Yang, Xiaoming; Dou, Yao; Liu, Zhongde

2013-04-07

Iodide, as a biologically important anion, it remains a worthwhile yet challenging undertaking to find a sensitive and specific approach to provide a technically simple iodide detection. In this article, it was found that no other ions than iodide-induced anisotropic growth of gold nanocrystals (AuNCs) originated from a small molecule, histidine-mediated synthesis of AuNCs, were observed. Simultaneously, it is accompanied by the fluorescence quenching of AuNCs and the naked-eye visible color change. Therefore, a new colorimetric and fluorometric sensing strategy was developed for the iodide-specific detection. Compared with currently reported methods, the present one displays the advantages of the visual detection and simplicity. The quenched fluorescence and enhanced surface plasmon resonance absorbance were found to be proportional to the iodide concentration over the range of 0.8-60 and 1.2-50 μM with a detection limit (3σ) of 118 nM and 215 nM, respectively.

Effect of the hydrogen charging of AISI 316 stainless steel from solutions containing As2 O3

International Nuclear Information System (INIS)

Brito, S.D. de.

1973-01-01

The hydrogen charging of AISI 316 stainless steel has turned unstable the austenitic structure which partially decomposes into two phases: ε (hexagonal close packed) and α ' (body centered cubic). A 1 N H 2 SO 4 solution was used as electrolyte, with varying concentrations of As 2 O 3 (0, 1, 5 and 100 mg/l) for a single constant applied current density (i o = 0,22 A/cm 2 ). It was observed that a smaller austenitic grain as well as a larger hydrogen charging time, improve the phase transformation. It was established that the order in which the transformation products of the austenite appear through hydrogen charging follows the sequence: Y → Y-bar + ε → Y + ε + α ', although there is still some doubt about the equivalent transformation order by plastic deformation. (author)

Achievement report for fiscal 1976 on Sunshine Program. Research on hydrogen production technology (Research on hydrogen production technology using thermochemical method); 1976 nendo suiso no seizo gijutsu no kenkyu seika hokokusho. Netsukagakuho ni yoru suiso seizo gijutsu no kenkyu

Energy Technology Data Exchange (ETDEWEB)

NONE

1977-03-01

This report covers part of the efforts to develop new hydrogen production technologies. Out of many processes involving Cu-halogen and alkali carbonate-iodine systems proposed as novel thermochemical processes, after they are compared with each other, a process of a sodium carbonate-iodine system with nickel in between is chosen. The chosen process is deemed to be the most excellent among the processes disclosed up to fiscal 1975. A feasibility study is conducted for the chosen process from the viewpoint of reaction rate, separation of reactive substances from each other, method for reaction manipulation, materials for device constitution, and thermal efficiency. As for the measurement of reaction rate for each unit reaction, basic reaction data are determined centering about the nickel iodide decomposition reaction and the sodium iodide carbonation reaction, and then reaction conditions which are roughly satisfying are obtained. A larger reaction unit is built in which the amounts of substances that come into reaction are approximately 10 times larger than those in the ones used in basic experiments. The progress of reactions is observed in the reaction unit, with the size enlarged in preparation for future construction of still larger reaction units. Methods for selectively isolating hydrogen out of gases ensuing from the decomposition are evaluated from the viewpoint of energy efficiency. In the selection of a reaction manipulation method, a single unit reaction process is advocated, and its thermal efficiency is estimated. (NEDO)

Electrokinetic properties and conductance relaxation of polystyrene and silver iodide plugs

NARCIS (Netherlands)

Hoven, van den J.J.

1984-01-01

This thesis describes an experimental study on the electrokinetic and electrical properties of concentrated polystyrene and silver iodide dispersions. The purpose of the study is to obtain information on the structure of the electrical double layer at the solid-liquid interface. Special

Study on hydrogen transfer in coal liquefaction by tritium and carbon-14 tracers

International Nuclear Information System (INIS)

Nitoh, Osamu; Kabe, Toshiaki; Kabe, Yaeko.

1985-01-01

For the analysis of mechanism of hydrogenation and cracking of coal, the liquefaction of Taiheiyo coal using tritium labeled gaseous hydrogen and tritium labeled tetralin with small amounts of carbon-14 labeled naphthalene has been studied. Taiheiyo coal(25g) was thermally decomposed in tetralin or naphthalene solvent(75g) at 400--440 0 C under the initial hydrogen pressure of 5.9MPa for 30min with Ni-Mo-Al 2 O 3 catalyst(0--5g). The reaction mixture in an autoclave was separated by filtration, distillation and solvent extraction. Produced gas, oils and the solvent were analyzed by gas chromatography. The tritium and carbon-14 contents of separated reaction products were measured with a liquid scintilation counter to study the hydrogen transfer mechanism. The distribution of reaction products and the amount of hydrogen transfer from gas or solvent to the products were also determined. In hydrogen donor solvent such as tetralin, the coal liquefaction yield was independent from the catalyst, but the catalyst was effective in hydrocracking of preasphaltene and asphaltene. In naphthalene solvent, the coal liquefaction reaction hardly occured in the absence of the catalyst, because hydrogen transfer from both the solvent and gaseous hydrogen was scarce. Tritium distribution in the reaction products showed that complicated hydrogen exchange reactions between gaseous hydrogen, coal liquids and solvent came out by the presence of coal liquids and catalyst. The very small amounts of carbon-14 transferred to the liquefaction products showed that carbon exchange or transfer between solvent and coal did not take place. (author)

Feasibility Study for the Reduction of Perchlorate, Iodide, and Other Aqueous Anions

National Research Council Canada - National Science Library

Clewell, Rebecca A; Tsui, David T; Mattie, David R

1999-01-01

Cyclic Voltammetry (CV) was used as a technique to determine the feasibility of the use of a coulometric detector in the determination of perchlorate, iodide, and various other anions commonly found in drinking water...

Iodide Residues in Milk Vary between Iodine-Based Teat Disinfectants

NARCIS (Netherlands)

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

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

PI3K activation is associated with intracellular sodium/iodide symporter protein expression in breast cancer

International Nuclear Information System (INIS)

Knostman, Katherine AB; McCubrey, James A; Morrison, Carl D; Zhang, Zhaoxia; Capen, Charles C; Jhiang, Sissy M

2007-01-01

The sodium/iodide symporter (NIS) is a membrane glycoprotein mediating active iodide uptake in the thyroid gland and is the molecular basis for radioiodide imaging and therapeutic ablation of thyroid carcinomas. NIS is expressed in the lactating mammary gland and in many human breast tumors, raising interest in similar use for diagnosis and treatment. However, few human breast tumors have clinically evident iodide uptake ability. We previously identified PI3K signaling as important in NIS upregulation in transgenic mouse models of breast cancer, and the PI3K pathway is commonly activated in human breast cancer. NIS expression, subcellular localization, and function were analyzed in MCF-7 human breast cancer cells and MCF-7 cells stably or transiently expressing PI3K p110alpha subunit using Western blot of whole cell lysate, cell surface biotinylation Western blot and immunofluorescence, and radioiodide uptake assay, respectively. NIS localization was determined in a human breast cancer tissue microarray using immunohistochemical staining (IHC) and was correlated with pre-existing pAkt IHC data. Statistical analysis consisted of Student's t-test (in vitro studies) or Fisher's Exact Test (in vivo correlational studies). In this study, we demonstrate that PI3K activation in MCF-7 human mammary carcinoma cells leads to expression of underglycosylated NIS lacking cell surface trafficking necessary for iodide uptake ability. PI3K activation also appears to interfere with cell surface trafficking of exogenous NIS as well as all-trans retinoic acid-induced endogenous NIS. A correlation between NIS expression and upregulation of PI3K signaling was found in a human breast cancer tissue microarray. Thus, the PI3K pathway likely plays a major role in the discordance between NIS expression and iodide uptake in breast cancer patients. Further study is warranted to realize the application of NIS-mediated radioiodide ablation in breast cancer

Fischer-Tropsch Performance of an SiO2-Supported Co-Based Catalyst Prepared by Hydrogen Dielectric-Barrier Discharge Plasma

International Nuclear Information System (INIS)

Fu Tingjun; Huang Chengdu; Lv Jing; Li Zhenhua

2014-01-01

A silica-supported cobalt catalyst was prepared by hydrogen dielectric-barrier discharge (H 2 -DBD) plasma. Compared to thermal hydrogen reduction, H 2 -DBD plasma treatment can not only fully decompose the cobalt precursor but also partially reduce the cobalt oxides at lower temperature and with less time. The effect of the discharge atmosphere on the property of the plasma-prepared catalyst and the Fischer-Tropsch synthesis activity was studied. The results indicate that H 2 -DBD plasma treatment is a promising alternative for preparing Co/SiO 2 catalysts from the viewpoint of energy savings and efficiency

Information Geometry of Positive Measures and Positive-Definite Matrices: Decomposable Dually Flat Structure

Directory of Open Access Journals (Sweden)

Shun-ichi Amari

2014-04-01

Full Text Available Information geometry studies the dually flat structure of a manifold, highlighted by the generalized Pythagorean theorem. The present paper studies a class of Bregman divergences called the (ρ,τ-divergence. A (ρ,τ -divergence generates a dually flat structure in the manifold of positive measures, as well as in the manifold of positive-definite matrices. The class is composed of decomposable divergences, which are written as a sum of componentwise divergences. Conversely, a decomposable dually flat divergence is shown to be a (ρ,τ -divergence. A (ρ,τ -divergence is determined from two monotone scalar functions, ρ and τ. The class includes the KL-divergence, α-, β- and (α, β-divergences as special cases. The transformation between an affine parameter and its dual is easily calculated in the case of a decomposable divergence. Therefore, such a divergence is useful for obtaining the center for a cluster of points, which will be applied to classification and information retrieval in vision. For the manifold of positive-definite matrices, in addition to the dually flatness and decomposability, we require the invariance under linear transformations, in particular under orthogonal transformations. This opens a way to define a new class of divergences, called the (ρ,τ -structure in the manifold of positive-definite matrices.

Non-radioactive determination of the penetration of methyl iodide through impregnated charcoals during dosing and purging

International Nuclear Information System (INIS)

Romans, J.B.; Deitz, V.R.

1979-01-01

A laboratory procedure is described using methyl iodide-127 which had the same linear flow of air (12.2 m/min) and contact time (0.25 sec.) as the RDT M16 Test Procedure. Only one-fourth of the charcoal was used (in a bed 2.54 cm diameter and 5.08 cm high) and the required dose of methyl iodide-127 was reduced from 5.25 to 1.31 mg. The inlet concentrations were determined with a gas chromatograph and the effluent concentrations with a modified microcoulombmeter. Two calibration procedures were used: (1) known vapor pressure of iodine crystals, and (2) quantitative pyrolysis of the methyl iodide-127 delivered from certified permeation tubes. Five charcoals and three impregnations were used in this study. Typical behaviors are given in 90% RH air with the charcoals either prehumidified for 16 hours at 90% RH or without the prehumidification. The breakthrough curves, concentration versus time, rose very slowly for the first 120 minutes and then more rapidly for an additional time. The lack of a dependence on the magnitude of the dose is compatible with a catalytic trapping mechanism. In the case of KI/sub x/ impregnations, there was excess emission of iodine during purging over that introduced as methyl iodide-127 which must have originated in the reservoir of iodine contained in the impregnation

Polymeric membrane sensors based on Cd(II) Schiff base complexes for selective iodide determination in environmental and medicinal samples.

Science.gov (United States)

Singh, Ashok Kumar; Mehtab, Sameena

2008-01-15

The two cadmium chelates of schiff bases, N,N'-bis(salicylidene)-1,4-diaminobutane, (Cd-S(1)) and N,N'-bis(salicylidene)-3,4-diaminotoluene (Cd-S(2)), have been synthesized and explored as ionophores for preparing PVC-based membrane sensors selective to iodide(I) ion. Potentiometric investigations indicate high affinity of these receptors for iodide ion. Polyvinyl chloride (PVC)-based membranes of Cd-S(1) and Cd-S(2) using as hexadecyltrimethylammonium bromide (HTAB) cation discriminator and o-nitrophenyloctyl ether (o-NPOE), dibutylphthalate (DBP), acetophenone (AP) and tributylphosphate (TBP) as plasticizing solvent mediators were prepared and investigated as iodide-selective sensors. The best performance was shown by the membrane of composition (w/w) of (Cd-S(1)) (7%):PVC (31%):DBP (60%):HTAB (2%). The sensor works well over a wide concentration range 5.3x10(-7) to 1.0x10(-2)M with Nernstian compliance (59.2mVdecade(-1) of activity) within pH range 2.5-9.0 with a response time of 11s and showed good selectivity for iodide ion over a number of anions. The sensor exhibits adequate life (3 months) with good reproducibility (S.D.+/-0.24mV) and could be used successfully for the determination of iodide content in environmental water samples and mouth wash samples.

Preliminary Design of Molecular Sieve for Removing Organic Iodide in Containment Filtered Venting System

Energy Technology Data Exchange (ETDEWEB)

Park, Tong Kyu; Shin, So Eun; Lee, Byung Chul [Heungdeok IT Valley Bldg., Yongin (Korea, Republic of); Kim, Hong Hyun; Lee, Kyung Jun [Gemvax and KAEL Inc., Daejeon (Korea, Republic of)

2014-05-15

In this paper, to increase the DF for gaseous iodine species, especially organic iodide, molecular sieve filled by silver exchanged zeolites is proposed and designed preliminarily. Its aerodynamic analysis is also performed and presented. In order to increase the DF for gaseous organic iodide, deep-bed type molecular sieve was proposed and designed preliminarily. Total 1,620kg of silver exchanged zeolites were filled evenly in 10 beds of the molecular sieve. The safety factor in the case of 20m{sup 3}/s will be smaller than the counterpart of the standard case (6m{sup 3}/s). However, if the adsorption capacity of the zeolites is larger than 3.09mg/g when the residence time is 0.09 second, the designed molecular sieve can be used at 20m3/s of volumetric flow rate. The removal efficiency for organic iodide should be considered as well as economical aspects in the design of molecular sieve. In the event of nuclear power plant (NPP) severe accident, the nuclear reactor containment might suffer damage resulting from overpressure caused by decay heat. In order to prevent this containment damage, containment venting has been considered as one of effective methods. However, since vented gases contain radioactive fission products, they should be filtered to be released to environment. Generally, containment filtered venting system (CFVS) is installed on NPP to achieve this aim. Even though great amount of efforts have been devoted to developing the CFVS using various filtering methods, the decontaminant factor (DF) for radioactive gaseous iodide is still unsatisfactory while DFs for radioactive aerosols and elemental iodine are very high.

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.

Iodide Sorption to Clays and the Relationship to Surface Charge and Clay Texture - 12356

Energy Technology Data Exchange (ETDEWEB)

Miller, Andrew; Kruichiak, Jessica; Tellez, Hernesto; Wang, Yifeng [Sandia National Laboratories, Albuquerque, NM 87185 (United States)

2012-07-01

Iodine is assumed to behave conservatively in clay barriers around nuclear waste repositories and in natural sediments. Batch experiments tend to show little to no sorption, while in column experiments iodine is often retarded relative to tritiated water. Current surface complexation theory cannot account for negatively charged ion sorption to a negatively charged clay particle. Surface protonation and iodide sorption to clay minerals were examined using surface titrations and batch sorption experiments with a suite of clay minerals. Surface titrations were completed spanning a range of both pH values and ionic strengths. For reference, similar titrations were performed on pure forms of an Al-O powder. The titration curves were deconvoluted to attain the pKa distribution for each material at each ionic strength. The pKa distribution for the Al-O shows two distinct peaks at 4.8 and 7.5, which are invariant with ionic strength. The pKa distribution of clays was highly variable between the different minerals and as a function of ionic strength. Iodide sorption experiments were completed at high solid:solution ratios to exacerbate sorption properties. Palygorskite and kaolinite had the highest amount of iodide sorption and montmorillonite had the least. (authors)

Organic iodide capture using a zeolite dry filtration

International Nuclear Information System (INIS)

Park, Sanggil; Sung, Joonyoung; Kim, Gi-ppeum; Lee, Jaeyoung

2017-01-01

An organic iodide, especially, methyl iodide (CH 3 I) would generated non-negligibly from a severe accident in a nuclear power plant. This CH 3 I will be dangerous for human when it was inhaled, it is highly toxic and causes a serious nerve disorder. Even it is a major contributor to a thyroid cancer. In order to prevent its environmental release, it is required to decontaminate using a filtration system. For the removal of CH 3 I from the release gases, wet-type is not ideal due to a high re-volatile characteristics of CH 3 I. It may become volatile after dissolving in a pool and forms CH 3 I again at the surface of water pool. Therefore, a dry-filtration should be installed to remove the CH 3 I. In this study, we preliminary investigate the characteristics of zeolite filtration methods for the removal of CH 3 I. We used both silver ion exchanged ZSM-5-zeolite (Ag+-ZSM-5) to study the effect of silver ion for the removal of iodine from CH 3 I. In summary, the CH 3 I capture tests using a silver ion exchanged zeolite was conducted in the coupled TGAGC test set-up. The mass change of the sample and concentration of CH 3 I were measured. The samples were investigated by the SEM/EDS to see its surface characteristics.

Studying the iodine leaching from the compositions based on epoxide resin and lead iodide

International Nuclear Information System (INIS)

Kalinin, N.N.; Elizarova, A.N.

1988-01-01

When studying iodine leaching, the possibility to use solid compositions, produced by incorporation of dry powdered lead iodide and its aqueous suspension into epoxide resin for long-term immobilization of iodine-129 under conditions of monitored storage, is evaluated. Analysis of the results obtained has shown that leaching rate in the first 4 days has the maximum value and constitutes (4.2 - 2700.0) x 10 -6 cm/day. Then the process of leaching is determined by diffusion mechanism. For samples, prepared by wet lead iodide incorporation the rate of leaching is higher than that of the corresponding samples prepared by dry compound incorporation

Formation of metastable phases in magnesium–titanium system by high-pressure torsion and their hydrogen storage performance

International Nuclear Information System (INIS)

Edalati, Kaveh; Emami, Hoda; Staykov, Aleksandar; Smith, David J.; Akiba, Etsuo; Horita, Zenji

2015-01-01

No binary phases exist in the Mg–Ti binary equilibrium phase diagram and the two elements are totally immiscible even in liquid form. This study shows that four metastable phases (two with the bcc and fcc structures and two with the hcp structures) are formed in the Mg–Ti system by severe plastic deformation (SPD) through the process of high-pressure torsion (HPT). Investigation of hydrogenation properties reveals that these metastable phases are decomposed to pure Mg and Ti during heating before they can absorb the hydrogen in the form of ternary Mg–Ti hydrides. First-principles calculations show that the hydrogenation reaction should occur thermodynamically, and ternary Mg–Ti hydrides with the cubic structure should form at low temperature. However, the slow kinetics for this reaction appears to be the limiting step. Calculations show that the binding energy of hydrogen increases and the thermodynamic stability of hydrides undesirably increases by addition of Ti to Mg

Enthalpies of potassium iodide dissolution in dimethyl acetamide mixtures with water

International Nuclear Information System (INIS)

Privalova, N.M.; Gritsenko, S.I.; Vorob'ev, A.F.

1986-01-01

Enthalpies of potassium iodide dissolution in mixed dimethyl acetamide - water solvent at 298.15 K in the whole range of dimethyl acetamide compositions are measured by the calorimetric method. From the plots of KI dissolution enthalpy dependence and dependence of experimental ΔH p∞ 0 value deviations from calculational ones on solvent composition, as well as from the results of calculation of solvate shell composition of potassium iodide ions in the mixed solvent, it is obvious that in the region of 0-15 mol% concentrations of dimethyl acetamide insufficient enrichment of solvate ion shells by dimethyl acetamide (DMAA) occurs, in the region of 15-40 mol% DMAA compositions enrichment of solvate shells of ions by water occurs, in the region of 40-100 mol% DMAA enrichment of solvate ion shells by the organic component in comparison with mixture compostion occurs. Maximum enrichment of solvate ion shells by mixture components in three above mentioned regions of the mixed solvent occurs at 10, 30 and 80 mol% DMAA concentrations

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…

Alkaline sodium borohydride gel as a hydrogen source for PEMFC or an energy carrier for NaBH 4-air battery

Science.gov (United States)

Liu, B. H.; Li, Z. P.; Chen, L. L.

In this preliminary study, we tried to use sodium polyacrylate as the super absorbent polymer to form alkaline NaBH 4 gel and explored its possibilities for borohydride hydrolysis and borohydride electro-oxidation. It was found that the absorption capacity of sodium polyacrylate decreased with increasing NaBH 4 concentration. The formed gel was rather stable in the sealed vessel but tended to slowly decompose in open air. Hydrogen generation from the gel was carried out using CoCl 2 catalyst precursor solutions. Hydrogen generation rate from the alkaline NaBH 4 gel was found to be higher and impurities in hydrogen were less than that from the alkaline NaBH 4 solution. The NaBH 4 gel also successfully powered a NaBH 4-air battery.

Insight to the Thermal Decomposition and Hydrogen Desorption Behaviors of NaNH2-NaBH4 Hydrogen Storage Composite.

Science.gov (United States)

Pei, Ziwei; Bai, Ying; Wang, Yue; Wu, Feng; Wu, Chuan

2017-09-20

The lightweight compound material NaNH 2 -NaBH 4 is regarded as a promising hydrogen storage composite due to the high hydrogen density. Mechanical ball milling was employed to synthesize the composite NaNH 2 -NaBH 4 (2/1 molar ratio), and the samples were investigated utilizing thermogravimetric-differential thermal analysis-mass spectroscopy (TG-DTA-MS), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR) analyses. The full-spectrum test (range of the ratio of mass to charge: 0-200) shows that the released gaseous species contain H 2 , NH 3 , B 2 H 6 , and N 2 in the heating process from room temperature to 400 °C, and possibly the impurity gas B 6 H 12 also exists. The TG/DTA analyses show that the composite NaNH 2 -NaBH 4 (2/1 molar ratio) is conductive to generate hydrogen so that the dehydrogenation process can be finished before 400 °C. Moreover, the thermal decomposition process from 200 to 400 °C involves two-step dehydrogenation reactions: (1) Na 3 (NH 2 ) 2 BH 4 hydride decomposes into Na 3 BN 2 and H 2 (200-350 °C); (2) remaining Na 3 (NH 2 ) 2 BH 4 reacts with NaBH 4 and Na 3 BN 2 , generating Na, BN, NH 3 , N 2 , and H 2 (350-400 °C). The better mechanism understanding of the thermal decomposition pathway lays a foundation for tailoring the hydrogen storage performance of the composite complex hydrides system.

Acute toxicity of live and decomposing green alga Ulva ( Enteromorpha) prolifera to abalone Haliotis discus hannai

Science.gov (United States)

Wang, Chao; Yu, Rencheng; Zhou, Mingjiang

2011-05-01

From 2007 to 2009, large-scale blooms of green algae (the so-called "green tides") occurred every summer in the Yellow Sea, China. In June 2008, huge amounts of floating green algae accumulated along the coast of Qingdao and led to mass mortality of cultured abalone and sea cucumber. However, the mechanism for the mass mortality of cultured animals remains undetermined. This study examined the toxic effects of Ulva ( Enteromorpha) prolifera, the causative species of green tides in the Yellow Sea during the last three years. The acute toxicity of fresh culture medium and decomposing algal effluent of U. prolifera to the cultured abalone Haliotis discus hannai were tested. It was found that both fresh culture medium and decomposing algal effluent had toxic effects to abalone, and decomposing algal effluent was more toxic than fresh culture medium. The acute toxicity of decomposing algal effluent could be attributed to the ammonia and sulfide presented in the effluent, as well as the hypoxia caused by the decomposition process.

Phenol degradation in aqueous solution by photolytic oxidation with ozone and/or hydrogen peroxide

International Nuclear Information System (INIS)

Koepp, T.; Koether, M.; Brueckner, B.; Radeke, K.H.

1993-01-01

The removal of phenol in an aqueous solution as a typical pollutant by oxidation using ozone and hydrogen peroxide under ultraviolet irradiation has been studied. Both the O 3 /UV and the H 2 O 2 /UV method can be powerful to decompose the total organic carbon (TOC) to carbon dioxide and water, but the first method is more effective. In the case of H 2 O 2 /UV method a strong overdose on H 2 O 2 is necessary to remove TOC effectively, however, a favourable H 2 O 2 concentration exists. This is probably caused by undesired parallel reactions of hydrogen peroxide. The simultaneous use of ozone and hydrogen peroxide accelerates the removal of TOC in the first third of experiment in comparison to the O 3 /UV method, but the time of total decomposition of TOC is delayed. A change in measured kinetics of ozone consumption by organic molecules corresponds well with the time of total transformation of aromatic into aliphatic substances. (orig.)

Rapid, specific determination of iodine and iodide by combined solid-phase extraction/diffuse reflectance spectroscopy

Science.gov (United States)

Arena, Matteo P.; Porter, Marc D.; Fritz, James S.

2002-01-01

A new, rapid methodology for trace analysis using solid-phase extraction is described. The two-step methodology is based on the concentration of an analyte onto a membrane disk and on the determination by diffuse reflectance spectroscopy of the amount of analyte extracted on the disk surface. This method, which is adaptable to a wide range of analytes, has been used for monitoring ppm levels of iodine and iodide in spacecraft water. Iodine is used as a biocide in spacecraft water. For these determinations, a water sample is passed through a membrane disk by means of a 10-mL syringe that is attached to a disk holder assembly. The disk, which is a polystyrene-divinylbenzene composite, is impregnated with poly(vinylpyrrolidone) (PVP), which exhaustively concentrates iodine as a yellow iodine-PVP complex. The amount of concentrated iodine is then determined in only 2 s by using a hand-held diffuse reflectance spectrometer by comparing the result with a calibration curve based on the Kubelka-Munk function. The same general procedure can be used to determine iodide levels after its facile and exhaustive oxidation to iodine by peroxymonosulfate (i.e., Oxone reagent). For samples containing both analytes, a two-step procedure can be used in which the iodide concentration is calculated from the difference in iodine levels before and after treatment of the sample with peroxymonosulfate. With this methodology, iodine and iodide levels in the 0.1-5.0 ppm range can be determined with a total workup time of approximately 60 s with a RSD of approximately 6%.

High Photon-to-Current Conversion in Solar Cells Based on Light-Absorbing Silver Bismuth Iodide.

Science.gov (United States)

Zhu, Huimin; Pan, Mingao; Johansson, Malin B; Johansson, Erik M J

2017-06-22

Here, a lead-free silver bismuth iodide (AgI/BiI 3 ) with a crystal structure with space group R3‾ m is investigated for use in solar cells. Devices based on the silver bismuth iodide deposited from solution on top of TiO 2 and the conducting polymer poly(3-hexylthiophene-2,5-diyl) (P3HT) as a hole-transport layer are prepared and the photovoltaic performance is very promising with a power conversion efficiency over 2 %, which is higher than the performance of previously reported bismuth-halide materials for solar cells. Photocurrent generation is observed between 350 and 700 nm, and the maximum external quantum efficiency is around 45 %. The results are compared to solar cells based on the previously reported material AgBi 2 I 7 , and we observe a clearly higher performance for the devices with the new silver and bismuth iodides composition and different crystal structure. The X-ray diffraction spectrum of the most efficient silver bismuth iodide material shows a hexagonal crystal structure with space group R3‾ m, and from the light absorption spectrum we obtain an indirect band gap energy of 1.62 eV and a direct band gap energy of 1.85 eV. This report shows the possibility for finding new structures of metal-halides efficient in solar cells and points out new directions for further exploration of lead-free metal-halide solar cells. © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.

Extraction and determination of hydrogen in uranium and zirconium; Extraction et dosage de l'hydrogene dans l'uranium et le zirconium

Energy Technology Data Exchange (ETDEWEB)

Champeix, L; Coblence, G; Darras, R [Commissariat a l' Energie Atomique, Saclay (France).Centre d' Etudes Nucleaires

1959-07-01

The method of desorption under vacuum at high temperatures in the solid phase, which gives good results in the case of steels, has been applied to uranium and zirconium. In these two metals hydrogen is found mainly in the form of hydride. It is chiefly a question of determining the most suitable temperature and the heating time necessary to obtain an almost total extraction of hydrogen. Two considerations must be taken into account in the choice of temperature. It should be such that on the one hand the hydride decomposes rapidly and completely at the reduced pressure applied, and on the other hand the diffusion of hydrogen through the metal takes place fairly quickly. The apparatus and the method used are described; systematic tests have led to the adoption of temperatures of 650 deg. C for uranium and 1050 deg. C for zirconium. (author) [French] La methode de desorption sous vide a chaud en phase solide, methode qui donne de bons resultats dans le cas des aciers, a ete appliquee a l'uranium et au zirconium. Dans ces deux metaux, l'hydrogene se trouve surtout a l'etat d'hydrure. Il s'agit essentiellement de determiner la temperature optimum et la duree du chauffage necessaire pour obtenir une extraction d'hydrogene pratiquement complete. Deux considerations interviennent dans le choix de la temperature. Elle doit etre telle que, d'une part la decomposition de l'hydrure se fasse rapidement et completement sous la pression reduite realisee et d'autre part que la diffusion de l'hydrogene a travers le metal soit assez rapide. L'appareil et le mode operatoire utilises sont decrits des essais systematiques ont conduit a adopter une temperature de 650 deg. C pour l'uranium et de 1050 deg. C pour le zirconium. (auteur)

Sterol regulatory element-binding proteins are regulators of the sodium/iodide symporter in mammary epithelial cells.

Science.gov (United States)

Wen, G; Pachner, L I; Gessner, D K; Eder, K; Ringseis, R

2016-11-01

The sodium/iodide symporter (NIS), which is essential for iodide concentration in the thyroid, is reported to be transcriptionally regulated by sterol regulatory element-binding proteins (SREBP) in rat FRTL-5 thyrocytes. The SREBP are strongly activated after parturition and throughout lactation in the mammary gland of cattle and are important for mammary epithelial cell synthesis of milk lipids. In this study, we tested the hypothesis that the NIS gene is regulated also by SREBP in mammary epithelial cells, in which NIS is functionally expressed during lactation. Regulation of NIS expression and iodide uptake was investigated by means of inhibition, silencing, and overexpression of SREBP and by reporter gene and DNA-binding assays. As a mammary epithelial cell model, the human MCF-7 cell line, a breast adenocarcinoma cell line, which shows inducible expression of NIS by all-trans retinoic acid (ATRA), and unlike bovine mammary epithelial cells, is widely used to investigate the regulation of mammary gland NIS and NIS-specific iodide uptake, was used. Inhibition of SREBP maturation by treatment with 25-hydroxycholesterol (5 µM) for 48h reduced ATRA (1 µM)-induced mRNA concentration of NIS and iodide uptake in MCF-7 cells by approximately 20%. Knockdown of SREBP-1c and SREBP-2 by RNA interference decreased the mRNA and protein concentration of NIS by 30 to 50% 48h after initiating knockdown, whereas overexpression of nuclear SREBP (nSREBP)-1c and nSREBP-2 increased the expression of NIS in MCF-7 cells by 45 to 60%, respectively, 48h after initiating overexpression. Reporter gene experiments with varying length of NIS promoter reporter constructs revealed that the NIS 5'-flanking region is activated by nSREBP-1c and nSREBP-2 approximately 1.5- and 4.5-fold, respectively, and activation involves a SREBP-binding motif (SRE) at -38 relative to the transcription start site of the NIS gene. Gel shift assays using oligonucleotides spanning either the wild-type or the

Decomposing changes in the aggregate labor force participation rate

OpenAIRE

Hotchkiss, Julie L.

2009-01-01

This paper presents a simple methodology for decomposing changes in the aggregate labor force participation rate (LFPR) over time into demographic group changes in labor force participation behavior and in population share. The purpose is to identify the relative importance of behavioral changes and population changes as driving forces behind changes in the aggregate LFPR.

Decomposing the variation of aggregate electricity intensity in Spanish industry

International Nuclear Information System (INIS)

Gonzalez, P.F.; Suarez, R.P.

2003-01-01

Several papers have dealt with methodological and application issues related to techniques for decomposing changes in environmental indicators. This paper aims to decompose changes in electricity intensity in Spanish industry and to explain the factors that contribute to these changes. Focusing on an energy intensity approach based on Divisia indices, we began by reviewing the two general parametric Divisia methods and six specific cases. In order to avoid obtaining significantly different results by using differing methods, all of them have been applied to Spanish data. Also two different disaggregation levels have been taken into consideration. Combined with electricity price analysis, the results of this paper indicate the poor contribution of structural change to substantial reductions in aggregate electricity intensity, and underline the role of innovation, development, diffusion and access to more efficient technologies as main contributors to the reduction of the energy/production ratio. (author)

The synthesis of 1-11C-labelled ethyl, propyl, butyl and isobutyl iodides and examples of alkylation reactions

International Nuclear Information System (INIS)

Laangstroem, B.; Antoni, G.; Gullberg, P.; Halldin, C.; Naagren, K.; Rimland, A.; Svaerd, H.

1986-01-01

New 11 C-labelled precursors [1- 11 C]ethyl,[1- 11 C]propyl, [1- 11 C]butyl, and [1- 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#percent# radiochemical yields and 65-95#percent# 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- 11 C-ethyl]iodocaine and N-[1- 11 C-butyl] bupivacaine. The synthesis of 3-nitrophenyl[1- 11 C]propyl ether is also presented in this paper as an example of an oxygen alkylation. (author)

Leaching of iodine from composites based on epoxy resin and lead iodide

International Nuclear Information System (INIS)

Kalinin, N.N.; Elizarova, A.N.

1988-01-01

The scope for using solid composites obtained by incorporating dry powdery lead iodide and its aqueous suspension into epoxy resin for prolonged immobilization of iodine-129 under monitorable storage conditions has been assessed by a study of leaching of iodine

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.

(II) complexes as sensitizers for dye sensitized solar cells

Indian Academy of Sciences (India)

dimethyl-3-propyl-1 H-imidazol-3-ium iodide (DMPII),. 4-tert-butyl-pyridine (TBP) and ... cymene) ruthenium(II) dimer was synthesized according to the reported ... saturated ammonium chloride (200 ml) solution was added to decompose the ...

Possible Role of Hydrogen in the Earth Core

Science.gov (United States)

Takahashi, E.; Imai, T.

2011-12-01

Possible role of hydrogen in the Earth core has been discussed by Stevenson (1977) and demonstrated experimentally by Fukai (1984), Okuchi (1997) and others. Planetary theory proposes a possibility of hydrogen incorporation in Earth's magma ocean from ambient solar nebula gas (Ikoma & Genda 2005, Genda & Ikoma 2008). More recently, migration of snow line during planet formation was examined (Min et al., 2010; Oka et al, 2011) and it was proposed that the Earth building material originally contained abundant water as ice and hydrous minerals. Therefore, it is very important to investigate the fate of water in the planet building process and clarify the role of hydrogen in the planetary core. Using SPring-8 synchrotron (NaCl capsule, LiAlH4 as hydrogen source), we determined the melting curve of FeH up to 20 GPa under hydrogen saturated conditions (Sakamaki, Takahashi et al, 2009). Observed melting point is below 1300C and has a very small dT/dP slope. By extrapolating the melting curve using Lindeman's law, we proposed that hydrogen could lower the melting temperature of the Earth core by more than 1500K than current estimate. Here we report our new experiments using SPring-8 synchrotron (single crystal diamond capsule, water as hydrogen source). Hydrogen concentration and melting temperature of FeHx that coexists with hydrous mantle minerals were determined at 15-20GPa and 1000-1600C. We show that 1) hydrogen concentration in FeHx at 1000C, coexisting with hydrous-B and ringwoodite is approximately X=0.6. 2) Upon heating, hydrous-B decomposes and hydrogen strongly partitions into FeHx (X=0.8~1.0) than ringwoodite. 3) FeHx that coexists with ringwoodite melts between ~1300C (solidus) and ~1600C (liquidus). Combined our new experiments with those by Sakamaki et al (2009) and Shibazaki et al (2009), partitioning of hydrogen between proto-core and primitive mantle is discussed. We propose that >90% of water in the source material may have entered the Earth core. Given

Experiments relating to hydrogen generated by corrosion processes associated with repositories for intermediate-level radioactive wastes

International Nuclear Information System (INIS)

Schenk, R.

1983-12-01

Organic components in an intermediate level waste repository decompose under both aerobic and anaerobic conditions to produce carbon dioxide, which may lead to acid corrosion of metallic containers and hence to hydrogen production. The possibility of hydrogen production within the repository must be considered in determining the long term safety. Thermodynamic calculations show that only pure water is required to produce hydrogen with iron in a repository. The hydrogen evolution rate is thus the important parameter. However, the available kinetic data is insufficient and needs to be supplemented experimentally. Carbon steel specimens were immersed in water over which several gas mixtures containing nitrogen, oxygen and carbon dioxide were passed; the amount of hydrogen picked up by the gas stream was measured. 1.4 - 28 ml hydrogen per square meter per hour was evolved when the gas mixture contained 1 and 20 volume per cent carbon dioxide respectively. Hydrogen was also detected in natural CO 2 -free water when oxygen concentration cells are present. No hydrogen could be detected at pH 8.5 and above. The experiments were all carried out at 25 degrees C and atmospheric pressure and restricted to the carbonate system. Natural waters contain a mixture of salts; this may increase or reduce the hydrogen evolution rate. Higher temperatures and pressures, in particular a higher partial pressure of carbon dioxide, will probably lead to an increase in the hydrogen evolution rate. (author)

Development program of hydrogen production by thermo-chemical water splitting is process

International Nuclear Information System (INIS)

Ryutaro Hino

2005-01-01

The Japan Atomic Energy Research Institute (JAERI) has been conducting R and D on the HTGR and also on thermo-chemical water splitting hydrogen production by using a iodine-sulfur cycle (IS process) in the HTTR project. The continuous hydrogen production for one week was demonstrated with a bench-scale test apparatus made of glass, and the hydrogen production rare was about 31 NL/h. Based on the test results and know-how obtained through the bench-scale test, a pilot test plant, which has a hydrogen production performance of 30 Nm 3 /h and will be operated under the high pressure up to 2 MPa, is being designed conceptually as the next step of the IS process development aiming to realize a future nuclear hydrogen production coupled with the HTGR. In this paper, we will introduce one-week continuous hydrogen production conducted with the bench-scale test apparatus and the pilot test program including R and D and an analytical system necessary for designing the pilot test plant. MW. Figure 1 shows an overview of the HTTR-IS plant. In this paper, we will introduce latest test results obtained with the bench-scale test apparatus and concepts of key components of the IS process, a sulfuric acid (H 2 SO 4 ) and a sulfur trioxide (SO 3 ) decomposers working under high-temperature corrosive circumstance, are also introduced as well as relating R and D and an analytical system for the pilot plant design. (authors)

Study of hydrogenation of Sm2Fe17-yGay by means of X-ray diffraction

International Nuclear Information System (INIS)

Teresiak, A.; Uhlemann, M.; Kubis, M.; Gebel, B.; Mattern, N.; Mueller, K.-H.

2000-01-01

The hydrogenation process of Sm 2 Fe 17-y Ga y (y=0-2) was studied. X-ray investigations show a decreasing hydrogen solubility in the intermetallic alloy with increasing Ga-content from 4.0±0.3 atoms per formula unit for Sm 2 Fe 17 to 2.85±0.05 for Sm 2 Fe 15 Ga 2 . The larger Ga atoms reduce the size of the interstitial sites and thereby the maximum hydrogen concentration is decreased. The behaviour of the lattice parameters a and c with increasing Ga content points to a changed hydrogen distribution on the interstitial sites, becoming more statistical. In situ observations by means of high temperature X-ray diffraction show that the hydrogen absorption process is diffusion controlled. The hydrogen absorption starts at an annealing temperature of 120-140 C in all cases. The solubility of hydrogen decreases with increasing temperature. The hydrogen is completely desorbed above 350 C in all cases. The absorption/desorption process is reversible between room temperature and 400 C. Annealing at temperatures above 400 C leads to the decomposition of the Sm 2 Fe 17 phase, indicated by emerging of α-Fe. The formation of SmH x is established at 600 C. The decomposition temperature increases with increasing Ga-content. Up to 750 C, only Sm 2 Fe 17 is completely decomposed. (orig.)

Lymphocutaneous Sporotrichosis Treated with Potassium Iodide with Development of Subclinical Hypothyroidism: Wolff-Chaikoff Effect?

Science.gov (United States)

Arora, Pooja; Raihan, M; Kubba, Asha; Gautam, Ram K

2017-01-01

Sporotrichosis is a subcutaneous mycotic infection caused by Sporothrix schenckii that is acquired by traumatic implantation. The diagnosis is established by demonstration of fungal elements on histopathology and culture. Potassium iodide, azole antifungals, and terbinafine are the treatment options available. In this article, we report a 60-year-old female with lymphocutaneous sporotrichosis that responded well to potassium iodide. However, subclinical hypothyroidism (Wolff-Chaikoff effect) was encountered as a side effect of therapy which was managed with thyroxine replacement. Knowledge about the Wolff-Chaikoff effect (WCE) is important for the dermatologist and reinforces the need for screening and monitoring of thyroid stimulating hormone (TSH) in patients where long duration therapy is being planned.

An Approach for Hydrogen Recycling in a Closed-loop Life Support Architecture to Increase Oxygen Recovery Beyond State-of-the-Art

Science.gov (United States)

Abney, Morgan B.; Miller, Lee; Greenwood, Zachary; Alvarez, Giraldo

2014-01-01

State-of-the-art atmosphere revitalization life support technology on the International Space Station is theoretically capable of recovering 50% of the oxygen from metabolic carbon dioxide via the Carbon Dioxide Reduction Assembly (CRA). When coupled with a Plasma Pyrolysis Assembly (PPA), oxygen recovery increases dramatically, thus drastically reducing the logistical challenges associated with oxygen resupply. The PPA decomposes methane to predominantly form hydrogen and acetylene. Because of the unstable nature of acetylene, a down-stream separation system is required to remove acetylene from the hydrogen stream before it is recycled to the CRA. A new closed-loop architecture that includes a PPA and downstream Hydrogen Purification Assembly (HyPA) is proposed and discussed. Additionally, initial results of separation material testing are reported.

Hydrogen iodide-based dry etching of GaAs, InP, and related compounds

International Nuclear Information System (INIS)

Pearton, S.J.; Chakrabarti, U.K.; Hobson, W.S.; Abernathy, C.R.; Katz, A.; Ren, F.; Fullowan, T.R.; Perley, A.P.

1992-01-01

In this paper HI/H 2 /Ar discharges are shown to be universal etchants for III-V semiconductors, giving rise to highly anisotropic features with smooth surface morphologies. At low dc Self bias (-V) and low pressure (1 mTorr), etch rates for all III-V materials of >2000 Angstrom · min -1 are possible for high HI percentages in the discharges, whereas rates greater than 1 μm · min -1 are obtained at higher pressures and dc biases. These etch rates are approximately an order of magnitude faster than for CH 4 /H 2 Ar mixtures under the same conditions and there is no polymer deposition on the mask or within the reactor chamber with HI/H 2 /Ar. Auger electron spectroscopy reveals residue-free, stoichiometric surfaces after dry etching in this mixture. As a result, photoluminescent intensities from dry etched samples remain high with little apparent damage introduction. Changes in the near-surface carrier concentration due to hydrogen passivation effects are also negligible with HI-based mixtures in comparison to CH 4 -based dry etching

Effects of trichostatin a on the expression of sodium/iodide symporter mRNA and the uptake of iodide in human thyroid cancer cell lines

International Nuclear Information System (INIS)

Bao Jiandong; Lin Xiufeng; Yu Huixin; Tan Cheng; Zhang Li

2010-01-01

Objective: To investigate the sodium/iodide symporter (NIS) expression and iodide uptake in thyroid cancer cells induced by the histone deacetyltransferase inhibitors (HDACi), Trichostatin A (TSA). Methods: Both the thyroid cancer cell lines, follicular thyroid carcinoma cell line FTC-133 and papillary thyroid carcinoma cell line K1, were firstly induced with TSA for 48 h. Then, the expression of NIS mRNA was analysed with reverse transcription-polymerase chain reaction (RT-PCR), the densitometric ratio of NIS/glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was calculated, and the iodide uptake in the thyroid cancer cells was also measured. Independent-sample t-test and one-way analysis of variance (ANOVA) were used to analyze the data. Results: For FTC-133 cells, increased NIS mRNA expression was detected after 48 h of TSA treatment, and the changes were dose-dependent (F=32.56, P 0.05). Furthermore, FTC-133 cells showed the ability of accumulating radioiodide with 50 and 75 nmol/L TSA induction for 48 h: (15.42 ± 0.42) x 10 3 counts · min -1 · 10 -5 cells vs (8.46 ± 0.84) x 10 3 counts · min -1 · 10 -5 cells, t=3.018, P 3 counts · min -1 · 10 -5 cells vs (8.46 ± 0.84) x 10 3 counts · min -1 · 10 -5 cells, t=3.557, P 3 counts · min -1 · 10 -5 cells, (6.97 ± 0.65) x 10 3 counts · min -1 · 10 -5 cells vs (5.37 ± 0.88) x 10 3 counts · min -1 · 10 -5 cells, t=0.185, P> 0.05 and t = 0.332, P > 0.05, respectively. Conclusion: TSA induced upregulated NIS mRNA expression in follicular thyroid cancer cells and augmented radioiodide uptake in thyroid cancer cells, while TSA had no remarkable effect on papillary thyroid carcinoma cell. (authors)

Root-induced decomposer growth and plant N uptake are not positively associated among a set of grassland plants

DEFF Research Database (Denmark)

Saj, S.; Mikola, J.; Ekelund, Flemming

2008-01-01

It is known that plant species can induce development of different soil decomposer communities and that they differ in their influence on organic matter decomposition and N mineralization in soil. However, no study has so far assessed whether these two observations are related to each other. Base...... that plant traits such as competitive ability for soil mineral N were more important for plant uptake of litter-N than those that directly affected the growth of soil decomposers.......It is known that plant species can induce development of different soil decomposer communities and that they differ in their influence on organic matter decomposition and N mineralization in soil. However, no study has so far assessed whether these two observations are related to each other. Based...... on the hypothesis that root-induced growth of soil decomposers leads to accelerated decomposition of SOM and increased plant N availability in soil, we predicted that (1) among a set of grassland plants the abundance of soil decomposers in the plant rhizosphere is positively associated with plant N uptake from soil...

Microbial Decomposers Not Constrained by Climate History Along a Mediterranean Climate Gradient

Science.gov (United States)

Baker, N. R.; Khalili, B.; Martiny, J. B. H.; Allison, S. D.

2017-12-01

The return of organic carbon to the atmosphere through terrestrial decomposition is mediated through the breakdown of complex organic polymers by extracellular enzymes produced by microbial decomposer communities. Determining if and how these decomposer communities are constrained in their ability to degrade plant litter is necessary for predicting how carbon cycling will be affected by future climate change. To address this question, we deployed fine-pore nylon mesh "microbial cage" litterbags containing grassland litter with and without local inoculum across five sites in southern California, spanning a gradient of 10.3-22.8° C in mean annual temperature and 100-400+ mm mean annual precipitation. Litterbags were deployed in October 2014 and collected four times over the course of 14 months. Recovered litter was assayed for mass loss, litter chemistry, microbial biomass, extracellular enzymes (Vmax and Km­), and enzyme temperature sensitivities. We hypothesized that grassland litter would decompose most rapidly in the grassland site, and that access to local microbial communities would enhance litter decomposition rates and microbial activity in the other sites along the gradient. We determined that temperature and precipitation likely interact to limit microbial decomposition in the extreme sites along our gradient. Despite their unique climate history, grassland microbes were not restricted in their ability to decompose litter under different climate conditions. Although we observed a strong correlation between bacterial biomass and mass loss across the gradient, litter that was inoculated with local microbial communities lost less mass despite having greater bacterial biomass and potentially accumulating more microbial residues. Our results suggest that microbial community composition may not constrain C-cycling rates under climate change in our system. However, there may be community constraints on decomposition if climate change alters litter chemistry, a

Phosphorus uptake by decomposing leaf detritus: effect of microbial biomass and activity

Energy Technology Data Exchange (ETDEWEB)

Mulholland, P J; Elwood, J W; Newbold, J D; Webster, J R; Ferren, L A; Perkins, R E

1984-12-01

The dominant energy source in small woodland streams is the allochthonous input of leaves. Utilization of this energy source by stream biota establishes the patterns of secondary productivity and nutrient uptake in these ecosystems. Although leaf inputs support much of the production of macroinvertebrates and higher consumers in streams, microbes are the critical link between these organisms and the leaf resource, much of which is undigestible by higher organisms. A number of studies have indicated that stream macroinvertebrates preferentially select leaves with greater levels of microbial activity. Rates of microbial activity associated with decomposing leaves were shown to be dependent on the supply of P in one woodland stream. In other streams, leaf decomposition has been shown to be nutrient limited as well. Thus, as in many other ecosystems, maintenance of high levels of production in streams is dependent on retention and efficient recycling of nutrients. Uptake of P by microbes colonizing leaves is an important mechanism for nutrient retention in small woodland streams. In these systems, numerous debris collections efficiently retard downstream movement of particulate materials, especially decomposing leaves. Uptake of dissolved, easily transportable forms of P by microbes attached to decomposing leaves increases P retention in streams. The more rapid the rate of P uptake onto decomposing leaves for a given P supply, the shorter the P uptake length and the more times an atom of P is utilized within a given stream reach. In this study the authors examined the temporal patterns of P uptake during the early stages of leaf decomposition in streams. Patterns of P uptake were compared to patterns of other measurements of microbial activity to identify the effect of microbial succession or conditioning of leaves on P uptake. 22 references, 1 figure, 2 tables.

Reactions of ferrate(VI) with iodide and hypoiodous acid: kinetics, pathways, and implications for the fate of iodine during water treatment.

Science.gov (United States)

Shin, Jaedon; von Gunten, Urs; Reckhow, David A; Allard, Sebastien; Lee, Yunho

2018-06-01

Oxidative treatment of iodide-containing waters can form iodinated disinfection by-products (I-DBPs) that are more toxic than the regulated DBPs. To better understand the fate of iodine during water treatment with ferrate(VI), kinetics, products, and stoichiometries for the reactions of ferrate(VI) with iodide (I - ) and hypoiodous acid (HOI) were determined. Ferrate(VI) showed considerable reactivities to both I - and HOI with higher reactivities at lower pH. Interestingly, the reaction of ferrate(VI) with HOI ( k = 6.0×10 3 M -1 s -1 at pH 9) was much faster than with I - ( k = 5.6×10 M -1 s -1 at pH 9). The main reaction pathway during treatment of I - -containing waters was the oxidation of I - to HOI and its further oxidation to IO 3 - by ferrate(VI). However, for pH > 9, the HOI disproportionation catalyzed by ferrate(VI) became an additional transformation pathway forming I - and IO 3 - . The reduction of HOI by hydrogen peroxide ( k = 2.0×10 8 M -1 s -1 for the reaction, HOI + HO 2 - → I - + O 2 + 2H + ), the latter being produced from ferrate(VI) decomposition, also contributes to the I - regeneration in the pH range 9 - 11. A kinetic model was developed that could well simulate the fate of iodine in the ferrate(VI)-I - system. Overall, due to a rapid oxidation of I - to IO 3 - with short-lifetimes of HOI, ferrate(VI) oxidation appears to be a promising option for I-DBP mitigation during treatment of I - -containing waters.

Comparison of expressed human and mouse sodium/iodide sym-porters reveals differences in transport properties and subcellular localization

Energy Technology Data Exchange (ETDEWEB)

Dayem, M.; Basquin, C.; Navarro, V.; Carrier, P.; Marsault, R.; Lindenthal, S.; Pourcher, T. [Univ Nice Sophia Antipolis, Sch Med, CEA, DSV, iBEB, SBTN, TIRO, F-06107 Nice (France); Chang, P. [CNRS, UPMC Biol Dev, UMR 7009, F-06230 Villefranche Sur Mer (France); Huc, S.; Darrouzet, E. [CEA Valrho, DSV, iBEB, SBTN, F-30207 Bagnols Sur Ceze (France)

2008-07-01

The active transport of iodide from the blood stream into thyroid follicular cells is mediated by the Na{sup +}/I{sup -} sym-porter (NIS). We studied mouse NIS (mNIS) and found that it catalyzes iodide transport into transfected cells more efficiently than human NIS (hNIS). To further characterize this difference,we compared {sup 125}I, uptake in the transiently transfected human embryonic kidney (HEK) 293 cells. We found that the Vmax for mNIS was four times higher than that for hNIS, and that the iodide transport constant (Km) was 2-5-fold lower for hNIS than mNIS. We also performed immuno-cyto-localization studies and observed that the subcellular distribution of the two ortho-logs differed. While the mouse protein was predominantly found at the plasma membrane, its human ortho-log was intracellular in {approx} 40% of the expressing cells. Using cell surface protein-labeling assays, we found that the plasma membrane localization frequency of the mouse protein was only 2-5-fold higher than that of the human protein, and therefore cannot alone account for,x values. We reasoned that the difference in the obtained Vmax the observed difference could also be caused by a higher turnover number for iodide transport in the mouse protein. We then expressed and analyzed chimeric proteins. The data obtained with these constructs suggest that the iodide recognition site could be located in the region extending from the N-terminus to transmembrane domain 8, and that the region between transmembrane domain 5 and the C-terminus could play a role in the subcellular localization of the protein. (authors)

Comparison of expressed human and mouse sodium/iodide sym-porters reveals differences in transport properties and subcellular localization

International Nuclear Information System (INIS)

Dayem, M.; Basquin, C.; Navarro, V.; Carrier, P.; Marsault, R.; Lindenthal, S.; Pourcher, T.; Chang, P.; Huc, S.; Darrouzet, E.

2008-01-01

The active transport of iodide from the blood stream into thyroid follicular cells is mediated by the Na + /I - sym-porter (NIS). We studied mouse NIS (mNIS) and found that it catalyzes iodide transport into transfected cells more efficiently than human NIS (hNIS). To further characterize this difference,we compared 125 I, uptake in the transiently transfected human embryonic kidney (HEK) 293 cells. We found that the Vmax for mNIS was four times higher than that for hNIS, and that the iodide transport constant (Km) was 2-5-fold lower for hNIS than mNIS. We also performed immuno-cyto-localization studies and observed that the subcellular distribution of the two ortho-logs differed. While the mouse protein was predominantly found at the plasma membrane, its human ortho-log was intracellular in ∼ 40% of the expressing cells. Using cell surface protein-labeling assays, we found that the plasma membrane localization frequency of the mouse protein was only 2-5-fold higher than that of the human protein, and therefore cannot alone account for,x values. We reasoned that the difference in the obtained Vmax the observed difference could also be caused by a higher turnover number for iodide transport in the mouse protein. We then expressed and analyzed chimeric proteins. The data obtained with these constructs suggest that the iodide recognition site could be located in the region extending from the N-terminus to transmembrane domain 8, and that the region between transmembrane domain 5 and the C-terminus could play a role in the subcellular localization of the protein. (authors)

Administration of additional inactive iodide during radioiodine therapy for Graves' disease. Who might benefit?

International Nuclear Information System (INIS)

Dietlein, M.; Moka, D.; Reinholz, U.; Schmidt, M.; Schomaecker, K.; Schicha, H.; Wellner, U.

2007-01-01

Aim: Graves' hyperthyroidism and antithyroid drugs empty the intrathyroid stores of hormones and iodine. The consequence is rapid 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 μg inactive potassium-iodide ( 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 131 I administration (M1) and 4 or 5 days later (M2) the following parameters were compared: effective 131 I half-life, thyroid dose, total T3, total T4, 131 I-activity in the T3- and T4-RIAs. Results: In Group A, the effective 131 I half-life M1 before iodine (3.81 ± 0.93 days) was significantly (p 131 I half-life M2 (4.65 ± 0.79 days). Effective 131 I half-life M1 correlated with the benefit from inactive 127 I (r = -0.79): Administration of 127 I was beneficial in patients with an effective 131 I half-life M1 of 131 I activity of T3 and T4 showed lower specific 131 I activity after addition of inactive iodine compared with patients from the same group with a lower initial specific 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 131 I T3 and y = 1.0827x - 0.4444 for 131 I T4) and steeper gradient for Group B (y = 0.6998x + 0.5417 for 131 I T3 and y = 1.3191x - 0.2901 for 131 I T4). Radioiodine therapy was successful in all 15 patients from Group A. Conclusion: The administration of 600 μg inactive iodide for three days during radioiodine therapy in patients with Graves' hyperthyroidism and an unexpectedly short half-life of <3 or 4 days was a safe

Oxidation of iodide and iodine on birnessite (delta-MnO2) in the pH range 4-8.

Science.gov (United States)

Allard, Sébastien; von Gunten, Urs; Sahli, Elisabeth; Nicolau, Rudy; Gallard, Hervé

2009-08-01

The oxidation of iodide by synthetic birnessite (delta-MnO(2)) was studied in perchlorate media in the pH range 4-8. Iodine (I(2)) was detected as an oxidation product that was subsequently further oxidized to iodate (IO(3)(-)). The third order rate constants, second order on iodide and first order on manganese oxide, determined by extraction of iodine in benzene decreased with increasing pH (6.3-7.5) from 1790 to 3.1M(-2) s(-1). Both iodine and iodate were found to adsorb significantly on birnessite with an adsorption capacity of 12.7 microM/g for iodate at pH 5.7. The rate of iodine oxidation by birnessite decreased with increasing ionic strength, which resulted in a lower rate of iodate formation. The production of iodine in iodide-containing waters in contact with manganese oxides may result in the formation of undesired iodinated organic compounds (taste and odor, toxicity) in natural and technical systems. The probability of the formation of such compounds is highest in the pH range 5-7.5. For pH iodine is quickly oxidized to iodate, a non-toxic and stable sink for iodine. At pH >7.5, iodide is not oxidized to a significant extent.

Determination of radiation dose rates and urinary activity of patients received Sodium Iodide-131 for treatment of differentiated thyroid carcinoma

International Nuclear Information System (INIS)

Beiki, D.; Shahhosseini, S.; Dadashzadeh, S.; Eftekhari, M.; Tayebi, H.; Moosazadeh-Rashti, G.

2004-01-01

Sodium Iodide-131 is administrated for treatment of hyperthyroidism and thyroid cancer. Iodine-131 has multiple routs of excretion (urine, saliva, sweat, milk, feces, exhalation) from the body. Patients receiving Sodium Iodide-131 therapy exposes other persons and the environment to unwanted radiation and contamination. The major sources of radiation dose from administration of Iodine-131 is external radiation , also there is a potential for exposure via contamination.Precautions are necessary to limit the radiation dose to family members, nursing staff and members of public and waste treatment workers to less than 1mSv. Patients received Sodium Iodide-131 may come into close contact with other persons. In order to derive appropriate recommendations, dose rates were measured from the anterior mid-trunk of 29 patients in the upright position with 15 minutes post-dose administration at 3 meters and just before they left the nuclear medicine department at 0.5, 1, and 3 meters. We have also measured urinary iodide excretion in 29 patients to estimate Sodium Iodide-131 urinary excretion pattern in iranian patients. Based on results, the maximum cumulative dose to nursing staff was on third day (leaving day) still less than recommended dose bye ICRP. The cumulative dose family members will be more but regarding the time and distance in close contact it will be also less than recommended dose by ICRP.Radiation dose rate was decreased significantly on third day. The urinary excretion patterns in all patients were similar. The urinary excretion rate-time curve in all patients showed multiple peaks due to retention and redistribution of Iodine-131 or enterohepatic cycle of radioiodinated thyroid hormones, which didn't allow calculation of urinary excretion rate constant. The results also showed that 67 hours post administration of Sodium Iodide-131 about 70% of radiopharmaceutical was excreted through urine, 28% physically decayed or eliminated through other biological

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.

Synergistic effect of helium and hydrogen for bubble swelling in reduced-activation ferritic/martensitic steel under sequential helium and hydrogen irradiation at different temperatures

Energy Technology Data Exchange (ETDEWEB)

Hu, Wenhui [Key Laboratory of Artificial Micro- and Nano-structures of Ministry of Education, Hubei Nuclear Solid Physics Key Laboratory and School of Physics and Technology, Wuhan University, Wuhan 430072 (China); Guo, Liping, E-mail: guolp@whu.edu.cn [Key Laboratory of Artificial Micro- and Nano-structures of Ministry of Education, Hubei Nuclear Solid Physics Key Laboratory and School of Physics and Technology, Wuhan University, Wuhan 430072 (China); Chen, Jihong; Luo, Fengfeng; Li, Tiecheng [Key Laboratory of Artificial Micro- and Nano-structures of Ministry of Education, Hubei Nuclear Solid Physics Key Laboratory and School of Physics and Technology, Wuhan University, Wuhan 430072 (China); Ren, Yaoyao [Center for Electron Microscopy, Wuhan University, Wuhan 430072 (China); Suo, Jinping; Yang, Feng [State Key Laboratory of Mould Technology, Institute of Materials Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China)

2014-04-15

Highlights: • Helium/hydrogen synergistic effect can increase irradiation swelling of RAFM steel. • Hydrogen can be trapped to the outer surface of helium bubbles. • Too large a helium bubble can become movable. • Point defects would become mobile and annihilate at dislocations at high temperature. • The peak swelling temperature for RAFM steel is 450 °C. - Abstract: In order to investigate the synergistic effect of helium and hydrogen on swelling in reduced-activation ferritic/martensitic (RAFM) steel, specimens were separately irradiated by single He{sup +} beam and sequential He{sup +} and H{sup +} beams at different temperatures from 250 to 650 °C. Transmission electron microscope observation showed that implantation of hydrogen into the specimens pre-irradiated by helium can result in obvious enhancement of bubble size and swelling rate which can be regarded as a consequence of hydrogen being trapped by helium bubbles. But when temperature increased, Ostwald ripening mechanism would become dominant, besides, too large a bubble could become mobile and swallow many tiny bubbles on their way moving, reducing bubble number density. And these effects were most remarkable at 450 °C which was the peak bubble swelling temperature for RAMF steel. When temperature was high enough, say above 450, point defects would become mobile and annihilate at dislocations or surface. As a consequence, helium could no longer effectively diffuse and clustering in materials and bubble formation was suppressed. When temperature was above 500, helium bubbles would become unstable and decompose or migrate out of surface. Finally no bubble was observed at 650 °C.

Synergistic effect of helium and hydrogen for bubble swelling in reduced-activation ferritic/martensitic steel under sequential helium and hydrogen irradiation at different temperatures

International Nuclear Information System (INIS)

Hu, Wenhui; Guo, Liping; Chen, Jihong; Luo, Fengfeng; Li, Tiecheng; Ren, Yaoyao; Suo, Jinping; Yang, Feng

2014-01-01

Highlights: • Helium/hydrogen synergistic effect can increase irradiation swelling of RAFM steel. • Hydrogen can be trapped to the outer surface of helium bubbles. • Too large a helium bubble can become movable. • Point defects would become mobile and annihilate at dislocations at high temperature. • The peak swelling temperature for RAFM steel is 450 °C. - Abstract: In order to investigate the synergistic effect of helium and hydrogen on swelling in reduced-activation ferritic/martensitic (RAFM) steel, specimens were separately irradiated by single He + beam and sequential He + and H + beams at different temperatures from 250 to 650 °C. Transmission electron microscope observation showed that implantation of hydrogen into the specimens pre-irradiated by helium can result in obvious enhancement of bubble size and swelling rate which can be regarded as a consequence of hydrogen being trapped by helium bubbles. But when temperature increased, Ostwald ripening mechanism would become dominant, besides, too large a bubble could become mobile and swallow many tiny bubbles on their way moving, reducing bubble number density. And these effects were most remarkable at 450 °C which was the peak bubble swelling temperature for RAMF steel. When temperature was high enough, say above 450, point defects would become mobile and annihilate at dislocations or surface. As a consequence, helium could no longer effectively diffuse and clustering in materials and bubble formation was suppressed. When temperature was above 500, helium bubbles would become unstable and decompose or migrate out of surface. Finally no bubble was observed at 650 °C

Polarographic determination of Iodide and Iodate, in Solutions Coming from Aerosols in Fission Products Containment Studies in Nuclear Power Stations

International Nuclear Information System (INIS)

Sanchez, M.; Ballesteros, O.; Fernandez, M.; Clavero, M.A.; Gonzalez, A.M.

2000-01-01

A polarographic method is described for the iodine species determination, iodide and iodate in water solutions. the iodate can be determined by differential pulse polarography. Calibration curves and the detection and determination limits have been obtained. Iodides is oxidized to iodate with sodium hypochlorite and the excess of oxidizing agent is destroyed with sodium sulphide. The concentration of iodide is calculated as the difference between the concentration of iodate in the sample before and after the oxidation. As an application, species of iodine in samples coming from the experimental plants GIRS (Gaseous Iodine Removal by Sprays) of Nuclear Fission Department of the CIEMAT, dedicated to fission products containment studies in nuclear power station, were determined. (Author) 10 refs

Solution enthalpy of potassium iodide in furfural and its mixtures with dimethylsulfoxide

International Nuclear Information System (INIS)

Vlasenko, K.K.; Belov, A.A.; Vorob'ev, A.F.

1986-01-01

Solution enthalpy of potassium iodide in furfural-dimethylsulfoxide mixtures at 298.15 K and furfural concentration 17.3-100% are determined experimentally. K + and I - ion solvate shell composition, which in the general case doesn't correspond to the mixed solvent composition, is calculated

Sensitive determination of iodide in the presence of large quantities of chloride

International Nuclear Information System (INIS)

Hainberger, L.; Lenzi, E.

1982-01-01

A determination of iodide with catalytic oxidation of p-phenetidine is described. A dye is formed with a maximum of absorption at 490 nm. The law of Lambert-Beer is obeyed between 0.6 and 2.2 ppm. Some of the interferents are examined. (Author)

Decomposing Oriented Graphs into Six Locally Irregular Oriented Graphs

DEFF Research Database (Denmark)

Bensmail, Julien; Renault, Gabriel

2016-01-01

An undirected graph G is locally irregular if every two of its adjacent vertices have distinct degrees. We say that G is decomposable into k locally irregular graphs if there exists a partition E1∪E2∪⋯∪Ek of the edge set E(G) such that each Ei induces a locally irregular graph. It was recently co...

Preparation of an ultra-fine, slightly dispersed silver iodide aerosol

International Nuclear Information System (INIS)

Poc, Marie-Martine

1973-01-01

A silver iodide aerosol was prepared under clean conditions. The method was to react iodine vapor with a silver aerosol in an inert dry atmosphere and in darkness. Great care was taken to avoid contamination from atmosphere air. The ice nucleating properties of the ultrafine AgI aerosol obtained were studied in a cloud mixing chamber: the aerosol was found to be strangely inactive. (author) [fr

Crystal growth and characterization of europium doped lithium strontium iodide scintillator as an ionizing radiation detector

Science.gov (United States)

Uba, Samuel

High performance detectors used in the detection of ionizing radiation is critical to nuclear nonproliferation applications and other radiation detectors applications. In this research we grew and tested Europium doped Lithium Strontium Iodide compound. A mixture of lithium iodide, strontium iodide and europium iodide was used as the starting materials for this research. Congruent melting and freezing temperature of the synthesized compound was determined by differential scanning calorimetry (DSC) using a Setaram Labsys Evo DSC-DTA instrument. The melting temperatures were recorded at 390.35°C, 407.59°C and freezing temperature was recorded at 322.84°C from a graph of heat flow plotted against temperature. The synthesized material was used as the charge for the vertical Bridgeman growth, and a 6.5 cm and 7.7cm length boule were grown in a multi-zone transparent Mullen furnace. A scintillating detector of thickness 2.53mm was fabricated by mechanical lapping in mineral oil, and scintillating response and timing were obtained to a cesium source using CS-137 isotope. An energy resolution (FWHM over peak position) of 12.1% was observed for the 662keV full absorption peak. Optical absorption in the UV-Vis wavelength range was recorded for the grown crystal using a U-2900 UV/VIS Spectrophotometer. Absorption peaks were recorded at 194nm, 273nm, and 344nm from the absorbance spectrum, various optical parameters such as absorption coefficient, extinction coefficient, refractive index, and optical loss were derived. The optical band gap energy was calculated using Tauc relation expression at 1.79eV.

Ascorbic acid as a bifunctional hydrogen bond donor for the synthesis of cyclic carbonates from CO2 under ambient conditions

KAUST Repository

Arayachukiat, Sunatda; Kongtes, Chutima; Barthel, Alexander; Vummaleti, Sai V. C.; Poater, Albert; Wannakao, Sippakorn; Cavallo, Luigi; D'Elia, Valerio

2017-01-01

Readily available ascorbic acid was discovered as an environmentally benign hydrogen bond donor (HBD) for the synthe-sis of cyclic organic carbonates from CO2 and epoxides in the presence of nucleophilic co-catalysts. The ascorbic acid/TBAI (TBAI: tetrabutylammonium iodide) binary system could be applied for the cycloaddition of CO2 to various epoxides under ambient or mild conditions. DFT calculations and catalysis experiments revealed an intriguing bifunctional mechanism in the step of CO2 insertion involving different hydroxyl moieties (enediol, ethyldiol) of the ascorbic acid scaffold.

Ascorbic acid as a bifunctional hydrogen bond donor for the synthesis of cyclic carbonates from CO2 under ambient conditions

KAUST Repository

Arayachukiat, Sunatda

2017-07-14

Readily available ascorbic acid was discovered as an environmentally benign hydrogen bond donor (HBD) for the synthe-sis of cyclic organic carbonates from CO2 and epoxides in the presence of nucleophilic co-catalysts. The ascorbic acid/TBAI (TBAI: tetrabutylammonium iodide) binary system could be applied for the cycloaddition of CO2 to various epoxides under ambient or mild conditions. DFT calculations and catalysis experiments revealed an intriguing bifunctional mechanism in the step of CO2 insertion involving different hydroxyl moieties (enediol, ethyldiol) of the ascorbic acid scaffold.

Performance of non-coconut base adsorbers in removal of iodine and organic iodides

International Nuclear Information System (INIS)

Rivers, R.D.; Pasha, M.; Fowler, E.E.; Goldsmith, J.M.

1975-01-01

Systems for the removal of radioactive iodine and organic iodides have used impregnated coconut shell activated carbons almost exclusively. Coconut shell carbons have some disadvantages: their geographical origin determines their trace chemical content; pore structures and impregnant effectiveness are highly dependent on activation and impregnation techniques. The authors report laboratory performance of a group of iodine-organic iodide adsorbers using bases other than coconut shell carbon. These have been evaluated in conformity with USAEC Regulatory Guide 1.52 and RDT M16 1T. Performance with regard to 131 I 2 and CH 3 131 I penetration and high-temperature elution have equaled or exceeded both the requirements of Guide 1.52 and results on typical coconut-shell carbons. Some performance outside Guide 1.52 ranges is included. Experimental problems in simulated LOCA testing are discussed. (U.S.)

Kinetic and Mechanistic Aspects of the Reactions of Iodide and Hypoiodous Acid with Permanganate: Oxidation and Disproportionation.

Science.gov (United States)

Zhao, Xiaodan; Salhi, Elisabeth; Liu, Huiling; Ma, Jun; von Gunten, Urs

2016-04-19

Oxidation kinetics of iodide and HOI/OI(-) by permanganate were studied in the pH range of 5.0-10.0. Iodide oxidation and iodate formation were faster at lower pH. The apparent second-order rate constants (k(obs)) for iodide oxidation by permanganate decrease with increasing pH from 29 M(-1) s(-1) at pH 5.0 and 6.9 M(-1) s(-1) at pH 7.0 to 2.7 M(-1) s(-1) at pH 10.0. k(obs) for HOI abatement are 56 M(-1) s(-1) at pH 5.0, 2.5 M(-1) s(-1) at pH 7.0, and 173 M(-1) s(-1) at pH 10.0. Iodate yields over HOI abatement decrease from 98% at pH 6.0 to 33% for pH ≥ 9.5, demonstrating that HOI disproportionation dominates HOI transformation by permanganate at pH ≥ 8.0. MnO2 formed as a product from permanganate reduction, oxidizes HOI to iodate for pH oxidation or disproportionation induced by MnO2 is much lower than for permanganate. During treatment of iodide-containing waters, the potential for iodinated disinfection byproducts (I-DBPs) formation is highest at pH 7.0-8.0 due to the long lifetime of HOI. For pH oxidized by permanganate to iodate, whereas for pH ≥ 8.0, HOI/OI(-) undergoes a fast permanganate-mediated disproportionation.

Production of high quality sodium iodide preparations labelled with carrier free iodine-125

International Nuclear Information System (INIS)

Abdukayumov, M.N.; Chistyakov, P.G.; Shilin, E.A.

2001-01-01

Work is related to the problem of high-quality Sodium Iodide preparation production and to the choice of the peptids iodination methods with the purpose of control test developing to determine the Biological activity of the above mentioned preparation

Design and reliability assessment of control systems for a nuclear-based hydrogen production plant with copper-chlorine thermochemical cycle

Energy Technology Data Exchange (ETDEWEB)

Al-Dabbagh, Ahmad W. [Faculty of Engineering and Applied Science, University of Ontario Institute of Technology, 2000 Simcoe Street North, Oshawa, Ontario, L1H 7K4 (Canada); Lu, Lixuan [Faculty of Energy Systems and Nuclear Science, Faculty of Engineering and Applied Science, University of Ontario Institute of Technology, 2000 Simcoe Street North, Oshawa, Ontario, L1H 7K4 (Canada)

2010-02-15

The thermochemical Copper-Chlorine (Cu-Cl) cycle is an emerging new method of nuclear-based hydrogen production. In the process, water is decomposed into hydrogen and oxygen through several physical and chemical processes. In this paper, a Distributed Control System (DCS) is designed for the thermochemical Cu-Cl cycle. The architecture and the communication networks of the DCS are discussed. Reliability of the DCS is assessed using fault trees. In the assessment, the impact of the malfunction of the actuators, sensors, controllers and communication networks on the overall system reliability is investigated. This provides key information for the selection of control system components, and determination of their inspection frequency and maintenance strategy. The hydrogen reactor unit, which is one of the major components in the thermochemical Cu-Cl cycle, is used to demonstrate the detailed design and analysis. (author)

A discrimination-association model for decomposing component processes of the implicit association test.

Science.gov (United States)

Stefanutti, Luca; Robusto, Egidio; Vianello, Michelangelo; Anselmi, Pasquale

2013-06-01

A formal model is proposed that decomposes the implicit association test (IAT) effect into three process components: stimuli discrimination, automatic association, and termination criterion. Both response accuracy and reaction time are considered. Four independent and parallel Poisson processes, one for each of the four label categories of the IAT, are assumed. The model parameters are the rate at which information accrues on the counter of each process and the amount of information that is needed before a response is given. The aim of this study is to present the model and an illustrative application in which the process components of a Coca-Pepsi IAT are decomposed.

1-(Ferrocen-1-ylmethyl-3-methylimidazol-3-ium iodide

Directory of Open Access Journals (Sweden)

Vincent O. Nyamori

2012-12-01

Full Text Available The structure of the title compound, [Fe(C5H5(C10H12N2]I, consists of a 1-(ferrocen-1-ylmethyl-3-methylimidazolium cation which is counter-balanced by an iodide anion. The cyclopentadienyl (Cp rings of the ferrocene unit have a slightly staggered conformation skewed from an ideal eclipsed conformation by an angle of 3.5 (6°. The interplanar angle between the Cp and the imidazole ring is 67.94 (2°.

Film formation of non-planar phthalocyanines on copper(i) iodide

OpenAIRE

Ramadan, A. J.; Fearn, S.; Jones, T. S. (Tim S.); Heutz, S.; Rochford, L. A. (Luke A.)

2016-01-01

Structural templating is frequently used in organic photovoltaic devices to control the properties of the functional layers and therefore improve efficiencies. Modification of the substrate temperatures has also been shown to impact the structure and morphology of phthalocyanine thin films. Here we combine templating by copper iodide and high substrate temperature growth and study its effect on the structure and morphology of two different non-planar phthalocyanines, chloroaluminium (ClAlPc) ...

Alkaline sodium borohydride gel as a hydrogen source for PEMFC or an energy carrier for NaBH{sub 4}-air battery

Energy Technology Data Exchange (ETDEWEB)

Liu, B.H. [Department of Materials and Engineering, Zhejiang University (China); Li, Z.P.; Chen, L.L. [Department of Chemical and Biochemical Engineering, Zhejiang University, Hangzhou 310027 (China)

2008-05-15

In this preliminary study, we tried to use sodium polyacrylate as the super absorbent polymer to form alkaline NaBH{sub 4} gel and explored its possibilities for borohydride hydrolysis and borohydride electro-oxidation. It was found that the absorption capacity of sodium polyacrylate decreased with increasing NaBH{sub 4} concentration. The formed gel was rather stable in the sealed vessel but tended to slowly decompose in open air. Hydrogen generation from the gel was carried out using CoCl{sub 2} catalyst precursor solutions. Hydrogen generation rate from the alkaline NaBH{sub 4} gel was found to be higher and impurities in hydrogen were less than that from the alkaline NaBH{sub 4} solution. The NaBH{sub 4} gel also successfully powered a NaBH{sub 4}-air battery. (author)

Rapid sonochemical preparation of shape-selective lead iodide

International Nuclear Information System (INIS)

Huang, Baojun; He, Qin; Fa, Wenjun; Li, Pinjiang; Zhang, Yange; Zheng, Zhi

2012-01-01

Graphical abstract: SEM morphologies of various PbI2 products obtained with the iodine concentration of 6.7 g/L and irradiation time of 1 minute at the reaction temperatures of 35 °C (a), 25 °C (b), and 15 °C (c). Highlights: ► PbI 2 with various morphologies were rapidly formed at room temperature. ► We could well control the morphologies of PbI 2 by changing reaction conditions. ► The PbI 2 films could better resist rolling in a liquid media. -- Abstract: Lead iodide (PbI 2 ) films/crystals with various nano/micro morphologies (e.g., Nanoflake, block and microrod) were rapidly synthesized by taking advantage of a simple sonochemical method. The PbI 2 crystals with uniform nanoflake structures could be fabricated directly on lead foils with the irradiation time as short as 36 s via interfacial reaction between lead foils and elemental iodine in ethanol at ambient temperature. It was found experimentally that the morphologies of the resulting thin films/crystals could be well controlled by the adjustment of several parameters including irradiation time, reaction solvents, iodine concentration, ultrasonic power, and reaction temperature. Most importantly, the resultant PbI 2 films are stable enough to resist rolling under the drastic ultrasound irradiation in a liquid media. This method is believed to be the fastest way for in situ fabrication of morphology-controlled semiconductor films on various metal substrates for subsequent applications related to the other metal iodide or metal sulfide semiconductor films.

A comparison between the secretion of Tc-99m pertechnetate and I-131 iodide through the stomach of the chacma monkey

International Nuclear Information System (INIS)

Ellmann, A.

1985-03-01

The way in which pertechnetate is excreted by the stomach is a continuing controversy in the nuclear medicine literature. The question arises: Does the stomach, unlike the thyroid handle pertechnetate and iodide by different mechanisms? The excretion of pertechnetate and iodide by the stomach in the Chacma baboon was compared. In this way an attempt was made to obtain more information on the way in which the stomach handles pertechnetate. The study was performed on young adult Chacma baboons. Pertechnetate and iodide were administeed simultaneously via the intravenous route. 6 Baboons were studied after pharmacological interventions, namely the administration of pentagastrin, cimetidine and perchlorate. Nine other baboons were studied after surgical interventions. Three groups of 3 each were studied after selective vagotomy, Billroth I gastrectomy and proximal gastrectomy respectively. In the surgical group post-operative studies were also done before and after pentagastrin stimulation. Tissue samples of the stomachs of 4 baboons were studied. The various types of surgery all resulted in a decrease in the volume of gastric juice. The excretion of pertechnetate and iodide was related to the volume of gastric juice except after the administration of perchlorate. In spite of marked changes of up to 60 times in the amount of pertechnetate and iodide excretion after the pharmacological and surgical interventions, the Tc : I - ratio remained almost constant. The Tc : I - ratio in the blood samples showed a gradual increase as could be expected. The Tc : I - ratios in the tissue samples were similar to those in the blood samples. It is indicated that, like iodide, pertechnetrat is probably excreted by the mucus cells of the stomach and not by the parietal cells. 28 figs., 164 refs., 6 tabs

Performance test of silver ion-exchanged zeolite for the removal of gaseous radioactive methyl iodide at high temperature condition

International Nuclear Information System (INIS)

Byung-Seon Choi; Geun-Il Park; Jung-Won Lee; Ho-Yeon Yang; Seung-Kon Ryu

2003-01-01

Performance tests of silver ion-exchanged zeolite (AgX) adsorbent for the control of radioiodine gas generated from a high-temperature process were carried out using both non-radioactive and a radioactive methyl iodide tracers. From the identification of SEM-EDAX analysis, an experimental result of silver ion-exchanged ratio containing 10∼30 wt% of Ag was fit to that calculated by the weight increment, and it was confirmed that the silver was uniformly distributed inside the pores of the adsorbent. Demonstration test of AgX-10 adsorbent using radioactive methyl iodide tracer was performed. The removal efficiency of radioiodine with AgX-10 in the temperature ranges of 150 to 300 deg C was in the ranges of 99.9% to 99.99%, except for 300 deg C. The influence of the long-term weathering and the poisoning with NO 2 gas (200 ppm) on adsorption capacity of AgX-10 was also analyzed. The removal efficiency of radioactive methyl iodide by AgX-10 weathered for 14 weeks was 99.95%. Long-term poisoning test showed that the adsorption efficiency of methyl iodide started to decrease after 10 weeks, and the removal efficiency of radioiodine by AgX-10, poisoned for 16 weeks, was 99% (DF=100). (author)

Impacts of warming on aquatic decomposers along a gradient of cadmium stress

International Nuclear Information System (INIS)

Batista, D.; Pascoal, C.; Cássio, F.

2012-01-01

We evaluated the effects of cadmium and temperature on plant-litter decomposition by examining diversity and activity of aquatic fungi and leaf consumption by Limnephilus sp., a typical invertebrate shredder of Iberian streams. Freshly fallen leaves were immersed in a stream to allow microbial colonization, and were exposed in microcosms to a gradient of cadmium (≤11 levels, ≤35 mg L −1 ). Microcosms were kept at 15 °C, a temperature typically found in Iberian streams in autumn, and at 21 °C to simulate a warming scenario. The increase in temperature stimulated leaf decomposition by microbes, fungal reproduction and leaf consumption by the shredder. Conversely, increased cadmium concentrations inhibited fungal reproduction and diversity, and leaf consumption by the invertebrate. Cadmium concentration inhibiting 50% of fungal reproduction, microbial decomposition and leaf consumption by the shredder was higher at 15 °C than at 21 °C, suggesting that higher temperatures can lead to increased metal toxicity to aquatic decomposers. - Highlights: ► We examined the effects of temperature and cadmium on aquatic detritus food-webs. ► Effects were assessed on plant-litter decomposition, fungi and invertebrate shredders. ► Results suggest that warming may increase cadmium toxicity to freshwater decomposers. - Global warming may increase cadmium toxicity to freshwater decomposers with implications to ecosystem processes.

Mercuric iodide sensor technology

International Nuclear Information System (INIS)

James, R.B.; Anderson, R.J.; Schlesinger, T.E.

1996-09-01

This report describes the improvement in the performance and the manufacturing yield of mercuric iodide detectors achieved by identifying the dominant impurities, carrier traps, and processing steps limiting device performance. Theoretical studies of electron and hole transport in this material set fundamental limits on detector performance and provided a standard against which to compare experimental results. Spectroscopy techniques including low temperature photoluminescence and thermally stimulated current spectroscopy were applied to characterize the deep level traps in this material. Traps and defects that can be introduced into the detector during growth, from the contact, and during the various steps in detector fabrication were identified. Trap energy levels and their relative abundances were determined. Variations in material quality and detector performance at the micron scale were investigated to understand the distribution in electric field in large volume detectors suitable for gamma-ray spectroscopy. Surface aging and contact degradation was studied extensively by techniques including atomic force microscopy, transmission electron microscopy, and variable angle spectroscopic ellipsometry. Preferred handling and processing procedures for maximizing detector performance and yield were established. The manufacturing yield of high resolution gamma-ray detectors was improved from a few percent to more than 30%

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.

Phase Stability and Electronic Structure of Prospective Sb-Based Mixed Sulfide and Iodide 3D Perovskite (CH3NH3)SbSI2.

Science.gov (United States)

Li, Tianyang; Wang, Xiaoming; Yan, Yanfa; Mitzi, David B

2018-06-29

Lead-free antimony-based mixed sulfide and iodide perovskite phases have recently been reported to be synthesized experimentally and to exhibit reasonable photovoltaic performance. Through a combination of experimental validation and computational analysis, we show no evidence of the formation of the mixed sulfide and iodide perovskite phase, MASbSI 2 (MA = CH 3 NH 3 + ), and instead that the main products are a mixture of the binary and ternary compounds (Sb 2 S 3 and MA 3 Sb 2 I 9 ). Density functional theory calculations also indicate that such a mixed sulfide and iodide perovskite phase should be thermodynamically less stable compared with binary/ternary anion-segregated secondary phases and less likely to be synthesized under equilibrium conditions. Additionally, band structure calculations show that this mixed sulfide and iodide phase, if possible to synthesize (e.g., under nonequilibrium conditions), should have a suitable direct band gap for photovoltaic application.

The influence of sodium salts (iodide, chloride and sulfate) on the formation efficiency of sulfamerazine nanocrystals.

Science.gov (United States)

Lou, Hao; Liu, Min; Qu, Wen; Johnson, James; Brunson, Ed; Almoazen, Hassan

2014-08-01

The purpose of this study is to evaluate the influence of sodium iodide, sodium chloride and sodium sulfate on the formation efficiency of sulfamerazine nanocrystals by wet ball milling. Sulfamerazine was milled using zirconium oxide beads in a solution containing polyvinylpyrrolidone (PVP) and a sodium salt (iodide, chloride or sulfate). Particle size distributions were evaluated by light diffraction before and after milling. High-performance liquid chromatography was utilized to determine the amount of PVP adsorbed onto sulfamerazine surface. Lyophilized nanocrystals were further characterized by differential scanning calorimetry and dissolution testing. Sulfate ion had more profound effect on reducing particle size via milling than iodide or chloride. We linked our findings to Hofmeister ion series, which indicates that sulfate ions tends to break the water structure, increases the surface tension and lowers the solubility of hydrocarbons in water. We hypothesized that the addition of sulfate ions dehydrated the PVP molecules and enhanced its adsorption onto the sulfamerazine particle surfaces. Consequently, the adsorbed PVP helped to stabilize of the nanosuspension. The nanocrystals that were obtained from the lyophilized milled suspensions exhibited a notable increase in dissolution rate. The addition of sodium sulfate enhanced the formation efficiency of sulfamerazine nanocrystals.

Simultaneous determination of bromide and iodide as acetone derivatives by gas chromatography and electron capture detection in natural waters and biological fluids

International Nuclear Information System (INIS)

Maros, L.; Kaldy, M.; Igaz, S.

1989-01-01

Oxidation of bromide and iodide ions in acidic solutions in the presence of acetone forms the corresponding acetone derivatives. Iodate was reduced with thiosulfate prior to the determination. After extraction with benzene the bromo- and iodoacetone were measured by gas chromatography using electron capture detection. The bromide and iodide contents of rainwater, drinking water, river water, seawater, oil brine, common salt, cow milk, and human blood serum were determined. The relative standard deviations for bromide at 10/sup /minus/7/ M and for iodide at 10/sup /minus/8/ M concentration were 1.9% and 3.0%, respectively, using 10-mL sample for the determination without preconcentration

Capture of organic iodides from nuclear waste by metal-organic framework-based molecular traps

KAUST Repository

Li, Baiyan; Dong, Xinglong; Wang, Hao; Ma, Dingxuan; Tan, Kui; Jensen, Stephanie; Deibert, Benjamin J.; Butler, Joseph; Cure, Jeremy; Shi, Zhan; Thonhauser, Timo; Chabal, Yves J.; Han, Yu; Li, Jing

2017-01-01

capture from nuclear waste. The capture mechanism was investigated by experimental and theoretical methods.Capturing radioactive organic iodides from nuclear waste is important for safe nuclear energy usage, but remains a significant challenge. Here, Li

Dynamics of production of iodine atoms by dissociation of iodides in a pulsed self-sustained discharge

International Nuclear Information System (INIS)

Vagin, Nikolai P; Kochetov, Igor' V; Napartovich, A P; Yuryshev, Nikolai N

2013-01-01

Absorption at the laser transition has been used for the first time to assess the evolution of concentration of iodine atoms in a pulsed self-sustained discharge in mixtures of iodides with a buffer gas such as molecular nitrogen and helium. Dynamics of the iodine atom production is studied by the method of absorption spectroscopy. The dissociation of C n F 2n+1 I and CnH 2n+1 I (n = 1, 2) iodides is investigated. The energy required to produce atomic iodine is evaluated. The experimental data obtained for CF 3 I are compared with the results of numerical simulations, their reasonable agreement being demonstrated. (active media)

Integrated approach to model decomposed flow hydrograph using artificial neural network and conceptual techniques

Science.gov (United States)

Jain, Ashu; Srinivasulu, Sanaga

2006-02-01

This paper presents the findings of a study aimed at decomposing a flow hydrograph into different segments based on physical concepts in a catchment, and modelling different segments using different technique viz. conceptual and artificial neural networks (ANNs). An integrated modelling framework is proposed capable of modelling infiltration, base flow, evapotranspiration, soil moisture accounting, and certain segments of the decomposed flow hydrograph using conceptual techniques and the complex, non-linear, and dynamic rainfall-runoff process using ANN technique. Specifically, five different multi-layer perceptron (MLP) and two self-organizing map (SOM) models have been developed. The rainfall and streamflow data derived from the Kentucky River catchment were employed to test the proposed methodology and develop all the models. The performance of all the models was evaluated using seven different standard statistical measures. The results obtained in this study indicate that (a) the rainfall-runoff relationship in a large catchment consists of at least three or four different mappings corresponding to different dynamics of the underlying physical processes, (b) an integrated approach that models the different segments of the decomposed flow hydrograph using different techniques is better than a single ANN in modelling the complex, dynamic, non-linear, and fragmented rainfall runoff process, (c) a simple model based on the concept of flow recession is better than an ANN to model the falling limb of a flow hydrograph, and (d) decomposing a flow hydrograph into the different segments corresponding to the different dynamics based on the physical concepts is better than using the soft decomposition employed using SOM.

Iodide selective membrane electrodes based on a Molybdenum-Salen as a neutral carrier

Energy Technology Data Exchange (ETDEWEB)

Ghanei-Motlagh, Masoud [Department of Chemistry, Shahid Bahonar University of Kerman, Kerman (Iran, Islamic Republic of); Taher, Mohammad Ali, E-mail: ma_taher@yahoo.com [Department of Chemistry, Shahid Bahonar University of Kerman, Kerman (Iran, Islamic Republic of); Ahmadi, Kyoumars [AJA University of Medical Sciences, Tehran (Iran, Islamic Republic of); Sheikhshoaie, Iran [Department of Chemistry, Shahid Bahonar University of Kerman, Kerman (Iran, Islamic Republic of)

2011-12-01

A new polymeric membrane electrode (PME) and a coated platinum disk electrode (CPtE) based on Schiff base complex of Mo(VI) as a suitable carrier for I{sup -} ion were described. The influence of membrane composition, pH and possible interfering anions were investigated on the response properties of the electrodes. The electrodes exhibited a Nernstian slope of 63.0 {+-} 0.5 (CPtE) and 60.3 {+-} 0.4 (PME) mV decade{sup -1} in I{sup -} ion over a wide concentration range from 7.9 x 10{sup -7} to 1.0 x 10{sup -1} M for CPtE and 9.1 x 10{sup -6} to 1.0 x 10{sup -1} M I{sup -} for PME. The potentiometric response of the electrodes was independent of the pH of the test solution in the pH range 2.0-8.5 with a fast response time (< 10 s). The process of transfer of iodide across the membrane interface was investigated by use of the AC impedance technique. The proposed sensors were successfully applied to direct determination of iodide in samples containing interfering anions, waste water and as indicator electrodes in precipitation titrations. Highlights: {yields} We study new selective membrane electrodes for iodide ions. {yields} To the best of our knowledge this is the first coated platinum disk electrode of I{sup -}. {yields} The sensors have a wide concentration range with a fast response time. {yields} Efforts have been made to improve the selectivity with the use of CPtE.

Charge Carrier Dynamics of Methylammonium Lead-Iodide Perovskite Solar Cells

OpenAIRE

Neukom, Martin Thomas

2016-01-01

Transient opto-electrical measurements of methylammonium lead iodide (MALI) perovskite solar cells (PSCs) are performed and analyzed in order to elucidate the operating mechanisms. The current response to a light pulse or voltage pulse shows an extraordinarily broad dynamic range covering 9 orders of magnitude in time - from microseconds to minutes - until steady-state is reached. Evidence of a slowly changing charge density at the perovskite layer boundaries is found, which is most probably ...

New thermophilic anaerobes that decompose crystalline cellulose

Energy Technology Data Exchange (ETDEWEB)

Taya, M; Hinoki, H; Suzuki, Y; Yagi, T; Yap, M G.S.; Kobayashi, T

1985-01-01

Two strains (designated as 25A and 3B) of cellulolytic, thermophilic, anaerobic, spore-forming bacteria were newly isolated from an alkaline hot spring through enrichment cultures at 60/sup 0/C. Though strain 25A was nearly identical to Clostridium thermocellum ATCC 27405 as a reference strain, strain 3B had some characteristics different from the reference; no flagellation, alkalophilic growth property (optimum pH of 7.5-8) and orange-colored pigmentation of the cell mass. Strain 3B effectively decomposed micro-crystalline cellulose (Avicel) and raw cellulosics (rice straw, newspaper, and bagasse) without physical or chemical pretreatments. 20 references, 2 figures, 2 tables.

A colorimetric method for highly sensitive and accurate detection of iodide by finding the critical color in a color change process using silver triangular nanoplates

Energy Technology Data Exchange (ETDEWEB)

Yang, Xiu-Hua; Ling, Jian, E-mail: lingjian@ynu.edu.cn; Peng, Jun; Cao, Qiu-E., E-mail: qecao@ynu.edu.cn; Ding, Zhong-Tao; Bian, Long-Chun

2013-10-10

Graphical abstract: -- Highlights: •Demonstrated a new colorimetric strategy for iodide detection by silver nanoplates. •The colorimetric strategy is to find the critical color in a color change process. •The colorimetric strategy is more accurate and sensitive than common colorimetry. •Discovered a new morphological transformation phenomenon of silver nanoplates. -- Abstract: In this contribution, we demonstrated a novel colorimetric method for highly sensitive and accurate detection of iodide using citrate-stabilized silver triangular nanoplates (silver TNPs). Very lower concentration of iodide can induce an appreciable color change of silver TNPs solution from blue to yellow by fusing of silver TNPs to nanoparticles, as confirmed by UV–vis absorption spectroscopy and transmission electron microscopy (TEM). The principle of this colorimetric assay is not an ordinary colorimetry, but a new colorimetric strategy by finding the critical color in a color change process. With this strategy, 0.1 μM of iodide can be recognized within 30 min by naked-eyes observation, and lower concentration of iodide down to 8.8 nM can be detected using a spectrophotometer. Furthermore, this high sensitive colorimetric assay has good accuracy, stability and reproducibility comparing with other ordinary colorimetry. We believe this new colorimetric method will open up a fresh insight of simple, rapid and reliable detection of iodide and can find its future application in the biochemical analysis or clinical diagnosis.

A colorimetric method for highly sensitive and accurate detection of iodide by finding the critical color in a color change process using silver triangular nanoplates

International Nuclear Information System (INIS)

Yang, Xiu-Hua; Ling, Jian; Peng, Jun; Cao, Qiu-E.; Ding, Zhong-Tao; Bian, Long-Chun

2013-01-01

Graphical abstract: -- Highlights: •Demonstrated a new colorimetric strategy for iodide detection by silver nanoplates. •The colorimetric strategy is to find the critical color in a color change process. •The colorimetric strategy is more accurate and sensitive than common colorimetry. •Discovered a new morphological transformation phenomenon of silver nanoplates. -- Abstract: In this contribution, we demonstrated a novel colorimetric method for highly sensitive and accurate detection of iodide using citrate-stabilized silver triangular nanoplates (silver TNPs). Very lower concentration of iodide can induce an appreciable color change of silver TNPs solution from blue to yellow by fusing of silver TNPs to nanoparticles, as confirmed by UV–vis absorption spectroscopy and transmission electron microscopy (TEM). The principle of this colorimetric assay is not an ordinary colorimetry, but a new colorimetric strategy by finding the critical color in a color change process. With this strategy, 0.1 μM of iodide can be recognized within 30 min by naked-eyes observation, and lower concentration of iodide down to 8.8 nM can be detected using a spectrophotometer. Furthermore, this high sensitive colorimetric assay has good accuracy, stability and reproducibility comparing with other ordinary colorimetry. We believe this new colorimetric method will open up a fresh insight of simple, rapid and reliable detection of iodide and can find its future application in the biochemical analysis or clinical diagnosis

Radioiodine source term and its potential impact on the use of potassium iodide

International Nuclear Information System (INIS)

Malinauskas, A.P.

1982-01-01

Information is presented concerning chemical forms of fission product iodine in the primary circuit; chemical forms of fission product iodine in the containment building; summary of iodine chemistry in light water reactor accidents; and impact of the radiodine source term on the potassium iodide issue

Regioselective conversion of primary alcohols into iodides in unprotected methyl furanosides and pyranosides

DEFF Research Database (Denmark)

Skaanderup, Philip Robert; Poulsen, Carina Storm; Hyldtoft, Lene

2002-01-01

Two methods are described for the regioselective displacement of the primary hydroxy group in methyl glycosides with iodide. The first method is a modification of a literature procedure employing triphenylphosphine and iodine, where purification has been carried out on a reverse phase column in o...

Extension of HPM Pulse Duration by Cesium Iodide Cathodes in Crossed Field Devices

National Research Council Canada - National Science Library

Benford, James

1998-01-01

.... The introduction of cathodes made from Cesium Iodide-coated (CsI) carbon fiber has shown plasma speeds reduced by factors of a few from uncoated carbon fiber, but previous work was at low diode fields of a few 10's of kV/cm...

HOW DO DEGRADABLE/BIODEGRADABLE PLASTIC MATERIALS DECOMPOSE IN HOME COMPOSTING ENVIRONMENT?

Directory of Open Access Journals (Sweden)

Magdalena Vaverková

2014-10-01

Full Text Available This paper provides information about biodegradability of polymeric (biodegradable/degradable materials advertised as 100%-degradable or certified as compostable, which may be a part of biodegradable waste, in home composting conditions. It describes an experiment that took place in home wooden compost bins and contained 9 samples that are commonly available in retail chains in the Czech Republic and Poland. The experiment lasted for the period of 12 weeks. Based on the results thereof it can be concluded that polyethylene samples with additive (samples 2, 4, 7 have not decomposed, their color has not changed and that no degradation or physical changes have occurred. Samples 1, 3 and 5 certified as compostable have not decomposed. Sample 6 exhibited the highest decomposition rate. Samples 8, 9 (tableware exhibited high degree of decomposition. The main conclusion from this study is that degradable/biodegradable plastics or plastics certified as compostable are not suitable for home composting.

Phase transition and hydrogen storage properties of Mg–Ga alloy

International Nuclear Information System (INIS)

Wu, Daifeng; Ouyang, Liuzhang; Wu, Cong; Wang, Hui; Liu, Jiangwen; Sun, Lixian; Zhu, Min

2015-01-01

Highlights: • A fully reversible transformation in Mg–Ga–H system with reduced dehydrogenation enthalpy is realized. • The mechanism of phase transformation in the de/hydrogenation of Mg–Ga alloy is revealed. • The de/hydrogenation process of Mg 5 Ga 2 compound is expressed as: Mg 5 Ga 2 + H 2 ↔ 2Mg 2 Ga + MgH 2 . - Abstract: Mg-based alloys are viewed as one of the most promising candidates for hydrogen storage; however, high desorption temperature and the sluggish kinetics of MgH 2 hinder their practical application. Alloying and changing the reaction pathway are effective methods to solve these issues. As the solid solubility of Ga in Mg is 5 wt% at 573 K, the preparation of a Mg(Ga) solid solution at relatively high temperatures was designed in this paper. The phase transition and hydrogen storage properties of the MgH 2 and Mg 5 Ga 2 composite (hereafter referred to as Mg–Ga alloy) were investigated by X-ray diffraction (XRD), pressure–composition-isotherm (PCI) measurements, and differential scanning calorimetry (DSC). The reversible hydrogen storage capacity of Mg–Ga alloy is 5.7 wt% H 2 . During the dehydrogenation process of Mg–Ga alloy, Mg 2 Ga reacts with MgH 2 , initially releasing H 2 and forming Mg 5 Ga 2 ; subsequently, MgH 2 decomposes into Mg with further release of H 2 . The phase transition mechanism of the Mg 5 Ga 2 compound during the dehydrogenation process was also investigated by using in situ XRD analysis. In addition, the dehydrogenation enthalpy and entropy changes, and the apparent activation energy were also calculated

Monochloramine determination using NN diethyl-p-phenylene-diamine. Influence of iodide traces

International Nuclear Information System (INIS)

Fiquet, J.M.

1980-09-01

When determining ''D.P.D.'' free oxidizers, the monochloramine interfers in particular for iodide levels analogous to those likely to be found in sea water. This is not so for iodate. The zero time extrapolation of the change in colour curve is one method that enables the method to be made more selective [fr

Determination of iodide with 1,3-dibromo-5,5-dimethylhydantoin (DBH) in comparison with the ICl-method. Analytical methods of pharmacopeias with DBH in respect to environmental and economical concern. Part 3.

Science.gov (United States)

Hilp, M; Senjuk, S

2001-06-01

USP 1995 (The United States Pharmacopeia, 23rd Edit., (1995), potassium iodide p. 1265, sodium iodide p. 1424), PH. EUR. 1997 (European Pharmacopoeia, third ed., Council of Europe, Strasbourg, (1997), potassium iodide p. 1367, sodium iodide p. 1493) and JAP 1996 (The Japanes Pharmacopoeia, 13th ed. (1996), potassium iodide p. 578, sodium iodide p. 630) determine iodide with the ICl-method (J. Am. Chem. Soc. 25 (1903) 756-761; Z. Anorg. Chem. 36 (1903) 76-83; Fresenius Z. Anal. Chem. 106 (1936) 12-23; Arzneibuch-Kommentar, Wissenschaftliche Erläuterungen zum Europäischen Arzneibuch, Wissenschaftliche Verlagsgesellschaft mbH, Stuttgart, Govi-Verlag - Pharmazeutischer Verlag GmbH, Eschborn, 12th suppl. (1999), K10 p. 2), using chloroform, which is toxic and hazardous to environment. Without the application of chlorinated hydrocarbons USP 2000 (The United State Pharmacopeia, 24th ed. (2000), potassium iodide p. 1368, sodium iodide p. 1535) and Brit 1999 (British Pharmacopoeia London, (1999), Appendix VIII C, p. A162) titrate iodide with the redox indicator amaranth. A titration with potentiometric indication giving two end-points at the step of I(2) and [ICl(2)](-) is described. Due to the high concentration of hydrochloric acid required for the ICl-method, the determination with DBH (1,3-dibromo-5,5-dimethylhydantoin; 1,3-dibromo-5,5-dimethyl-2,4-imidazolidinedione) can be recommended and is performed easily. Similarly, the iodide content of gallamine triethiodide may be analyzed with DBH by application of a visual two-phase titration in water and ethyl acetate or with potentiometric indication in a mixture of 2-propanol and water. During the removal of the excess of DBH 4-bromo-triethylgallamine (2,2',2"-[1-bromo-benzene-2,3,4-triyltris(oxy)]N,N,N-triethylethanium) is formed.

AAO-CNTs electrode on microfluidic flow injection system for rapid iodide sensing.

Science.gov (United States)

Phokharatkul, Ditsayut; Karuwan, Chanpen; Lomas, Tanom; Nacapricha, Duangjai; Wisitsoraat, Anurat; Tuantranont, Adisorn

2011-06-15

In this work, carbon nanotubes (CNTs) nanoarrays in anodized aluminum oxide (AAO-CNTs) nanopore is integrated on a microfluidic flow injection system for in-channel electrochemical detection of iodide. The device was fabricated from PDMS (polydimethylsiloxane) microchannel bonded on glass substrates that contains three-electrode electrochemical system, including AAO-CNTs as a working electrode, silver as a reference electrode and platinum as an auxiliary electrode. Aluminum, stainless steel catalyst, silver and platinum layers were sputtered on the glass substrate through shadow masks. Aluminum layer was then anodized by two-step anodization process to form nanopore template. CNTs were then grown in AAO template by thermal chemical vapor deposition. The amperometric detection of iodide was performed in 500-μm-wide and 100-μm-deep microchannels on the microfluidic chip. The influences of flow rate, injection volume and detection potential on the current response were optimized. From experimental results, AAO-CNTs electrode on chip offers higher sensitivity and wider dynamic range than CNTs electrode with no AAO template. Copyright © 2011 Elsevier B.V. All rights reserved.

Solvent-Free Synthesis of Aryl Iodide Using Nano SiO2/HIO4 as a Reusable Acid Catalyst

Directory of Open Access Journals (Sweden)

A. Bamoniri

2014-07-01

Full Text Available An efficient and environmentally benign   method for the synthesis of aryl iodides have been developed by diazotization of aromatic amines with NaNO2 and nanosilica periodic acid (nano-SPIA as a green catalyst via grinding followed by a sandmeyer iodination by KI under solvent-free conditions at room temperature. The ensuing aryl diazonium salts supported on nano-SPIA were sufficiently stable to be kept at room temperature in the dry state. This method is a novel, efficient, eco-friendly route for solvent-free synthesis of aryl iodides.

Reactions of dihydridotetrakis(triphenylphosphine)ruthenium(II) with olefins and isolation of new ruthenium-olefin complexes

International Nuclear Information System (INIS)

Komiya, Sanshiro; Yamamoto, Akio

1976-01-01

Dihydridotetrakis(triphenylphosphine)ruthenium (II), RuH 2 (PPh 3 ) 4 , reacts with olefins (ethylene, propylene, stylene and butadiene) to give olefin-coordinated complexes of the type, Ru(olefin)(PPh 3 ) 3 and equimolar amounts of their hydrogenation products per mol of the dihydride complex. The olefin coordinated with ruthenium can be exchanged with other olefins. Olefin-coordinated complexes easily react with molecular hydrogen to afford tetrahydridotris(triphenylphosphine)ruthenium, RuH 4 (PPh 3 ) 3 , releasing alkane at room temperature, Under hydrogen atmosphere catalytic hydrogenation of the olefins smoothly takes place with RuH 2 (PPh 3 ) 4 . (Ethylene)tris(triphenylphosphine)ruthenium(0) reacts with methyl iodide to give propylene and a trace of butadiene along with methane, ethylene, and small amounts of ethane and butenes. The formation of propylene suggests that oxidative addition involving cleavage of the C-H bond of ethylene to ruthenium giving a hydridovinyl complex may be taking place. Reactions of Ru(C 2 H 4 )(PPh 3 ) 3 with methyl-d 3 iodide and ethyl iodide, and of Ru(C 3 H 6 )(PPh 3 ) 3 with methyl iodide were examined to test the generality of this type of reaction. The reaction of Ru(C 2 H 4 )(PPh 3 ) 3 with CD 3 I released CD 4 and CD 2 H 2 together with CD 3 H suggesting the involvement of α-hydrogen abstraction. (auth.)

Decomposing University Grades: A Longitudinal Study of Students and Their Instructors

Science.gov (United States)

Beenstock, Michael; Feldman, Dan

2018-01-01

First-degree course grades for a cohort of social science students are matched to their instructors, and are statistically decomposed into departmental, course, instructor, and student components. Student ability is measured alternatively by university acceptance scores, or by fixed effects estimated using panel data methods. After controlling for…

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.

Inversion symmetry and bulk Rashba effect in methylammonium lead iodide perovskite single crystals

KAUST Repository

Frohna, Kyle

2018-05-02

Methylammonium lead iodide perovskite (MAPbI3) exhibits long charge carrier lifetimes that are linked to its high efficiency in solar cells. Yet, the mechanisms governing these unusual carrier dynamics are not completely understood. A leading hypothesis-disproved in this work-is that a large, static bulk Rashba effect slows down carrier recombination. Here, using second harmonic generation rotational anisotropy measurements on MAPbI3 crystals, we demonstrate that the bulk structure of tetragonal MAPbI3 is centrosymmetric with I4/mcm space group. Our calculations show that a significant Rashba splitting in the bandstructure requires a non-centrosymmetric lead iodide framework, and that incorrect structural relaxations are responsible for the previously predicted large Rashba effect. The small Rashba splitting allows us to compute effective masses in excellent agreement with experiment. Our findings rule out the presence of a large static Rashba effect in bulk MAPbI3, and our measurements find no evidence of dynamic Rashba effects.

Abstraction of iodine from aromatic iodides by alkyl radicals: steric and electronic effects.

Science.gov (United States)

Dolenc, Darko; Plesnicar, Bozo

2006-10-13

Abstraction of the iodine atom from aryl iodides by alkyl radicals takes place in some cases very efficiently despite the unfavorable difference in bond dissociation energies of C-I bonds in alkyl and aryl iodides. The abstraction is most efficient in iodobenzenes, ortho-substituted with bulky groups. The ease of abstraction can be explained by the release of steric strain during the elimination of the iodine atom. The rate of abstraction correlates fairly well with the strain energy, calculated by density functional theory (DFT) and Hartree-Fock (HF) methods as a difference in the total energy of ortho and para isomers. However, besides the steric bulk, the presence of some other functional groups in an ortho substituent also influences the rate. The stabilization of the transition state, resembling a 9-I-2 iodanyl radical, by electron-withdrawing groups seems to explain a positive sign of the Hammett rho value in the radical abstraction of halogen atoms.

Sodium iodide symporter (NIS) in extrathyroidal malignancies: focus on breast and urological cancer

International Nuclear Information System (INIS)

Micali, Salvatore; Bulotta, Stefania; Puppin, Cinzia; Territo, Angelo; Navarra, Michele; Bianchi, Giampaolo; Damante, Giuseppe; Filetti, Sebastiano; Russo, Diego

2014-01-01

Expression and function of sodium iodide symporter (NIS) is requisite for efficient iodide transport in thyrocytes, and its presence in cancer cells allows the use of radioiodine as a diagnostic and therapeutic tool in thyroid neoplasia. Discovery of NIS expression in extrathyroidal tissues, including transformed cells, has opened a novel field of research regarding NIS-expressing extrathyroidal neoplasia. Indeed, expression of NIS may be used as a biomarker for diagnostic, prognostic, and therapeutic purposes. Moreover, stimulation of endogenous NIS expression may permit the radioiodine treatment of extrathyroidal lesions by concentrating this radioisotope. This review describes recent findings in NIS research in extrathyroidal malignancies, focusing on breast and urological cancer, emphasizing the most relevant developments that may have clinical impact. Given the recent progress in the study of NIS regulation as molecular basis for new therapeutic approaches in extrathyroidal cancers, particular attention is given to studies regarding the relationship between NIS and clinical-pathological aspects of the tumors and the regulation of NIS expression in the experimental models

Inversion symmetry and bulk Rashba effect in methylammonium lead iodide perovskite single crystals

KAUST Repository

Frohna, Kyle; Deshpande, Tejas; Harter, John; Peng, Wei; Barker, Bradford A.; Neaton, Jeffrey B.; Louie, Steven G.; Bakr, Osman; Hsieh, David; Bernardi, Marco

2018-01-01

Methylammonium lead iodide perovskite (MAPbI3) exhibits long charge carrier lifetimes that are linked to its high efficiency in solar cells. Yet, the mechanisms governing these unusual carrier dynamics are not completely understood. A leading hypothesis-disproved in this work-is that a large, static bulk Rashba effect slows down carrier recombination. Here, using second harmonic generation rotational anisotropy measurements on MAPbI3 crystals, we demonstrate that the bulk structure of tetragonal MAPbI3 is centrosymmetric with I4/mcm space group. Our calculations show that a significant Rashba splitting in the bandstructure requires a non-centrosymmetric lead iodide framework, and that incorrect structural relaxations are responsible for the previously predicted large Rashba effect. The small Rashba splitting allows us to compute effective masses in excellent agreement with experiment. Our findings rule out the presence of a large static Rashba effect in bulk MAPbI3, and our measurements find no evidence of dynamic Rashba effects.

Methods to prevent the source term of methyl lodide during a core melt accident

Energy Technology Data Exchange (ETDEWEB)

Karhu, A. [VTT Energy (Finland)

1999-11-01

The purpose of this literature review is to gather available information of the methods to prevent a source term of methyl iodide during a core melt accident. The most widely studied methods for nuclear power plants include the impregnated carbon filters and alkaline additives and sprays. It is indicated that some deficiencies of these methods may emerge. More reactive impregnants and additives could make a great improvement. As a new method in the field of nuclear applications, the potential of transition metals to decompose methyl iodide, is introduced in this review. This area would require an additional research, which could elucidate the remaining questions of the reactions. The ionization of the gaseous methyl iodide by corona-discharge reactors is also shortly described. (au)

Solvation effect on decomposition rate of 10-methyl-10-phenylphenoxarsonium iodide in some alcohols and ketones

International Nuclear Information System (INIS)

Gavrilov, V.I.; Gumerov, N.S.; Rakhmatullin, R.R.

1989-01-01

By the method of conductometry decomposition kinetics of 10-methyl-10phenylphenoxarsonium iodide in methanol, ethanol, 2-propanol, 1-butanol, 1-pentanol and methyl ethyl ketone at initial concentration of the salt 0.00024-0.003 mol/l, is studied. It is shown that at the temperatures up to 80-95 deg C practically no decomposition of arsonium salt in methanol and ethanol is observed. With an increase in the length of alcohol alkyl radical the decomposition rate increases. The values of activation enrgy both for alcohols and ketone are approximately the same. At the same time, decomposition rate in alcohol proved much slower than in ketone, which is related to iodide-ion solvation in protic solvents

Solvation effect on decomposition rate of 10-methyl-10-phenylphenoxarsonium iodide in some alcohols and ketones

Energy Technology Data Exchange (ETDEWEB)

Gavrilov, V I; Gumerov, N S; Rakhmatullin, R R [Kazanskij Khimiko-Tekhnologicheskij Inst., Kazan (USSR)

1989-03-01

By the method of conductometry decomposition kinetics of 10-methyl-10phenylphenoxarsonium iodide in methanol, ethanol, 2-propanol, 1-butanol, 1-pentanol and methyl ethyl ketone at initial concentration of the salt 0.00024-0.003 mol/l, is studied. It is shown that at the temperatures up to 80-95 deg C practically no decomposition of arsonium salt in methanol and ethanol is observed. With an increase in the length of alcohol alkyl radical the decomposition rate increases. The values of activation enrgy both for alcohols and ketone are approximately the same. At the same time, decomposition rate in alcohol proved much slower than in ketone, which is related to iodide-ion solvation in protic solvents.

POTENTIAL FOR HYDROGEN BUILDUP IN HANFORD SEALED AIR FILLED NUCLEAR STORAGE VESSELS

International Nuclear Information System (INIS)

HEY BE

2008-01-01

This calculation is performed in accordance with HNF-PRO-8259, PHMC Calculation Preparation and Issue and addresses the question as to whether a flammable mixture of hydrogen gas can accumulate in a Hanford sealed nuclear storage vessel where the only source of hydrogen is the moisture in the air that initially filled the vessel Of specific concern is nuclear fuel inside IDENT 69-Gs, placed in Core Component Containers (CCCs) located inside Interim Storage Vaults (ISVs) at the Plutonium Finishing Plant (PFP) The CCCs are to be removed from the ISVs and placed inside a Hanford Unirradiated Fuel Package (HUFP) for transport and interim storage. The repackaging procedures mandated that no plastics were permitted, all labels and tape were to be removed and the pins to be clean and inspected Loading of the fuel into the CCC/ISV package was permitted only if it was not raining or snowing. This was to preclude the introduction of any water The purpose was to minimize the presence of any hydrogenous material inside the storage vessels. The scope of NFPA 69, 'Standard on Explosion Prevention Systems', precludes its applicability for this case. The reactor fuel pins are helium bonded. The non-fuel pins, such as the pellet stacks, are also helium bonded. The fuel pellets were sintered at temperatures that preclude any residual hydrogenous material. Hydrogen gas can be formed from neutron and gamma radiolysis of water vapor. The radiolysis reaction is quite complex involving several intermediate radicals, and competing recombination reactions. Hydrogen gas can also be formed through corrosion. This analysis takes a simplistic approach and assumes that all water vapor present in the storage vessel is decomposed into hydrogen gas. Although the analysis is needed to specifically address HUFP storage of nuclear fuel, it is equally applicable to any sealed fuel storage vessel under the assumptions listed

Methanogenesis from acetate by Methanosarcina barkeri: Catalysis of acetate formation from methyl iodide, CO/sub 2/, and H/sub 2/ by the enzyme system involved

Energy Technology Data Exchange (ETDEWEB)

Laufer, K; Eikmanns, B; Frimmer, U; Thauer, R K

1987-04-01

Cell suspensions of Methanosarcina barkeri grown on acetate catalyze the formation of methane and CO/sub 2/ from acetate as well as an isotopic exchange between the carboxyl group of acetate and CO/sub 2/. Here we report that these cells also mediate the synthesis of acetate from methyl iodide, CO/sub 2/, and reducing equivalents (H/sub 2/ or CO), the methyl group of acetate being derived from methyl iodide and the carboxyl group from CO/sub 2/. Methyl chloride and methyltosylate but not methanol can substitute for methyl iodide in this reaction. Acetate formation from methyl iodide, CO/sub 2/, and reducing equivalents is coupled with the phosphorylation of ADP. Evidence is presented that methyl iodide is incorporated into the methyl group of acetate via a methyl corrinoid intermediate (deduced from inhibition experiments with propyl iodide) and that CO/sub 2/ is assimilated into the carboxyl group via a C/sub 1/ intermediate which does not exchange with free formate or free CO. The effects of protonophores, of the proton-translocating ATPase inhibitor N,N'-dicyclohexylcarbodiimide, and of arsenate on acetate formation are interpreted to indicate that the reduction of CO/sub 2/ to the oxidation level of the carboxyl group of acetate requires the presence of an electrochemical proton potential and that acetyl-CoA or acetyl-phosphate rather than free acetate is the immediate product of the condensation reaction. These results are dicsussed with respect to the mechanism of methanogenesis from acetate.

Assessment of a colorimetric method for the measurement of low concentrations of peracetic acid and hydrogen peroxide in water.

Science.gov (United States)

Domínguez-Henao, Laura; Turolla, Andrea; Monticelli, Damiano; Antonelli, Manuela

2018-06-01

The recent growing interest in peracetic acid (PAA) as disinfectant for wastewater treatment demands reliable and readily-available methods for its measurement. In detail, the monitoring of PAA in wastewater treatment plants requires a simple, accurate, rapid and inexpensive measurement procedure. In the present work, a method for analyzing low concentrations of PAA, adapted from the US EPA colorimetric method for total chlorine, is assessed. This method employs N,N-diethyl-p-phenylelnediamine (DPD) in the presence of an excess of iodide in a phosphate buffer system. Pink colored species are produced proportionally to the concentration of PAA in the sample. Considering that PAA is available commercially as an equilibrium solution of PAA and hydrogen peroxide (H 2 O 2 ), a measurement method for H 2 O 2 is also investigated. This method, as the one for the determination of PAA, is also based on the oxidation of iodide to iodine, with the difference that ammonium molybdate Mo(VI) is added to catalyze the oxidation reaction between H 2 O 2 and iodide, quantifying the total peroxides (PAA+ H 2 O 2 ). The two methods are suitable for concentration ranges from about 0.1-1.65 mg L -1 and from about 0.3-3.3 mg L -1 , respectively for PAA and H 2 O 2 . Moreover, the work elucidates some relevant aspects related to the operational conditions, kinetics and the possible interference of H 2 O 2 on PAA measurement. Copyright © 2018 Elsevier B.V. All rights reserved.

Methods for assessing the impact of avermectins on the decomposer community of sheep pastures.

Science.gov (United States)

King, K L

1993-06-01

This paper outlines methods which can be used in the field assessment of potentially toxic chemicals such as the avermectins. The procedures focus on measuring the effects of the drug on decomposer organisms and the nutrient cycling process in pastures grazed by sheep. Measurements of decomposer activity are described along with methods for determining dry and organic matter loss and mineral loss from dung to the underlying soil. Sampling methods for both micro- and macro-invertebrates are discussed along with determination of the percentage infection of plant roots with vesicular-arbuscular mycorrhizal fungi. An integrated sampling unit for assessing the ecotoxicity of ivermectin in pastures grazed by sheep is presented.

Concentration and electrode material dependence of the voltammetric response of iodide on platinum, glassy carbon and boron-doped diamond in the room temperature ionic liquid 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide

International Nuclear Information System (INIS)

Bentley, Cameron L.; Bond, Alan M.; Hollenkamp, Anthony F.; Mahon, Peter J.; Zhang, Jie

2013-01-01

The electro-oxidation of iodide has been investigated as a function of concentration using steady-state microelectrode voltammetry, transient cyclic voltammetry and linear-sweep semi-integral voltammetry on platinum, glassy carbon and boron-doped diamond electrodes in the room temperature ionic liquid 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide. Two oxidation processes are observed on all of the investigated electrode materials, with the first being assigned to the oxidation of iodide to triiodide (confirmed by UV/visible spectroscopy) and the second being attributed to the oxidation of triiodide to iodine. Iodide oxidation is kinetically more facile on platinum compared to glassy carbon or boron-doped diamond. At elevated bulk iodide concentrations, the nucleation and growth of sparingly soluble electrogenerated iodine at the electrode surface was observed and imaged in situ using optical microscopy. The diffusion coefficient of iodide was determined to be 2.59 (±0.04) × 10 −7 cm 2 s −1 and independent of the bulk concentration of iodide. The steady-state iodide oxidation current measured at a platinum microelectrode was found to be a linear function of iodide concentration, as expected if there are no contributions from non-Stokesian mass-transport processes (electron hopping and/or Grotthuss-type exchange) under the investigated conditions

Synthesis and Characterization of Methylammonium Lead Iodide Perovskite and its Application in Planar Hetero-junction Devices

Science.gov (United States)

Upadhyaya, Aditi; Mohan Singh Negi, Chandra; Yadav, Anjali; Gupta, Saral K.; Singh Verma, Ajay

2018-06-01

The present paper reports on the synthesis and characterization of methylammonium lead iodide perovskite thin film and its applications in heterojunction devices. Perovskite thin films were deposited by a simple spin-coating method using a precursor solution including methyl ammonium iodide and lead iodide onto a glass substrate. The surface morphology study via field emission scanning electron microscopy of the perovskite thin film shows complete surface coverage on glass substrate with negligible pin-holes. UV–visible spectroscopy study revealed a broad absorption range and the exhibition of a band-gap of 1.6 eV. The dark current-voltage (I–V) characteristics of all the devices under study show rectifying behaviour similar to the Schottky diode. Various device parameters such as ideality factor and barrier height are extracted from the I–V curve. At low voltages the devices exhibit Ohmic behaviour, trap free space charge limited conduction governs the charge transport at an intermediate voltage range, while at much higher voltages the devices show trap controlled space charge limited conduction. Furthermore, impedance spectroscopy measurements enable us to extract the various internal parameters of the devices. Correlations between these parameters and I–V characteristics are discussed. The different capacitive process arising in the devices was discussed using the capacitance versus frequency curve.

EPR investigation of zinc/iodine exchange between propargyl iodides and diethylzinc: detection of propargyl radical by spin trapping.

Science.gov (United States)

Maury, Julien; Jammi, Suribabu; Vibert, François; Marque, Sylvain R A; Siri, Didier; Feray, Laurence; Bertrand, Michèle

2012-10-19

The production of propargyl radicals in the reaction of dialkylzincs with propargyl iodides in nondegassed medium was investigated by EPR using tri-tert-butylnitrosobenzene (TTBNB) as a spin trap. The radical mechanism and the nature of the observed species were confirmed by the trapping of propargyl radicals generated by an alternative pathway: i.e., upon irradiation of propargyl iodides in the presence of hexa-n-butyldistannane. In dialkylzinc-mediated experiments a high concentration of adduct was instantaneously observed, whereas no spontaneous production of spin adduct was detected in a blank experiment performed with the propargylic iodide and TTBNB in the absence of diethylzinc. Under irradiation in the presence of distannane, two different species were observed at the very beginning of the irradiation; the nitroxide resulting from the trapping of propargyl radical at the propargyl carbon remained the only species detected after irradiating for several minutes. The absence of adducts resulting from the trapping of allenyl canonical forms was supported by DFT calculations and by the preparation of an authentic sample.

Photoinduced electron transfer and solvation in iodide-doped acetonitrile clusters.

Science.gov (United States)

Ehrler, Oli T; Griffin, Graham B; Young, Ryan M; Neumark, Daniel M

2009-04-02

We have used ultrafast time-resolved photoelectron imaging to measure charge transfer dynamics in iodide-doped acetonitrile clusters I(-)(CH(3)CN)(n) with n = 5-10. Strong modulations of vertical detachment energies were observed following charge transfer from the halide, allowing interpretation of the ongoing dynamics. We observe a sharp drop in the vertical detachment energy (VDE) within 300-400 fs, followed by a biexponential increase that is complete by approximately 10 ps. Comparison to theory suggests that the iodide is internally solvated and that photodetachment results in formation of a diffuse electron cloud in a confined cavity. We interpret the initial drop in VDE as a combination of expansion of the cavity and localization of the excess electron on one or two solvent molecules. The subsequent increase in VDE is attributed to a combination of the I atom leaving the cavity and rearrangement of the acetonitrile molecules to solvate the electron. The n = 5-8 clusters then show a drop in VDE of around 50 meV on a much longer time scale. The long-time VDEs are consistent with those of (CH(3)CN)(n)(-) clusters with internally solvated electrons. Although the excited-state created by the pump pulse decays by emission of a slow electron, no such decay is seen by 200 ps.

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

Phase equilibria of toluene/heptane with deep eutectic solvents based on ethyltriphenylphosphonium iodide for the potential use in the separation of aromatics from naphtha

International Nuclear Information System (INIS)

Kareem, Mukhtar A.; Mjalli, Farouq S.; Hashim, Mohd Ali; Hadj-Kali, Mohamed K.O.; Ghareh Bagh, Fatemeh Saadat; Alnashef, Inas M.

2013-01-01

Highlights: • Ionic liquid analogues are introduced as potential replacements for ionic liquids. • Deep eutectic solvents presented in this work were successful for extracting aromatics. • Hand correlation was applied to ascertain the experimental measurements. • The NRTL thermodynamic model was capable for correlating the LLE experimental data. -- Abstract: In this work, the liquid–liquid extraction of toluene from hydrocarbons mixtures (toluene/heptane) was investigated using deep eutectic solvents as solvents. Ethyltriphenylphosphonium iodide as a salt with either ethylene glycol or sulfolane as hydrogen-bond donors (HBDs) were utilized for synthesizing six DESs. (Liquid + liquid) equilibria data were determined experimentally for the ternary system (toluene + heptane + DES) at (30, 40, 50, and 60) °C and atmospheric pressure. Hand correlation was applied to establish the reliability of the experimental data. In many cases the correlation factor is found close to unity which indicates high reliability of the data. The selectivities and distribution coefficients were used to determine the suitability of these DESs as solvents for this extraction process. Higher selectivities than those published for sulfolane as a commercial solvent were observed. The DES made from ethyltriphenylphosphonium iodide and sulfolane at salt:HBD of 1:4 showed the best separation capability at 30 °C. Thus, it was further characterized by measuring its viscosity and refractive index at a range of temperatures to help understand its physical behaviour needed for process design. The non-random two-liquid (NRTL) model was applied successfully to correlate the experimental tie-lines and to calculate the phase compositions of the ternary systems. It has been found that the third non-randomness parameter varies linearly with the HBD number of moles

Decomposing series-parallel graphs into paths of length 3 and triangles

DEFF Research Database (Denmark)

Merker, Martin

2015-01-01

An old conjecture by Jünger, Reinelt and Pulleyblank states that every 2-edge-connected planar graph can be decomposed into paths of length 3 and triangles, provided its size is divisible by 3. We prove the conjecture for a class of planar graphs including all 2-edge-connected series-parallel gra...

Kinetic features of cadmium electrodeposition in iodide water-acetone electrolytes

International Nuclear Information System (INIS)

Kuznetsov, V.V.; Skibina, L.M.; Khalikov, R.R.

2006-01-01

Based on the data of chronopotentiometric, galvanostatic, potentiodynamic, and impedance measurements, the composition of aqueous acetone electrolyte is studied for its effect on the rate of cadmium(II) electroreduction in iodide media. The adsorption of I - ions on the cadmium cathode surface is shown to depend on the interaction mechanism between the components of water-acetone mixtures. During a competitive adsorption of anions and organic solvent molecules, this affects the mechanism and the rate of electrodeposition and also the coating quality [ru

Formation of Multiple-Phase Catalysts for the Hydrogen Storage of Mg Nanoparticles by Adding Flowerlike NiS.

Science.gov (United States)

Xie, Xiubo; Ma, Xiujuan; Liu, Peng; Shang, Jiaxiang; Li, Xingguo; Liu, Tong

2017-02-22

In order to enhance the hydrogen storage properties of Mg, flowerlike NiS particles have been successfully prepared by solvothermal reaction method, and are subsequently ball milled with Mg nanoparticles (NPs) to fabricate Mg-5 wt % NiS nanocomposite. The nanocomposite displays Mg/NiS core/shell structure. The NiS shell decomposes into Ni, MgS and Mg 2 Ni multiple-phases, decorating on the surface of the Mg NPs after the first hydrogen absorption and desorption cycle at 673 K. The Mg-MgS-Mg 2 Ni-Ni nanocomposite shows enhanced hydrogenation and dehydrogenation rates: it can quickly uptake 3.5 wt % H 2 within 10 min at 423 K and release 3.1 wt % H 2 within 10 min at 573 K. The apparent hydrogen absorption and desorption activation energies are decreased to 45.45 and 64.71 kJ mol -1 . The enhanced sorption kinetics of the nanocomposite is attributed to the synergistic catalytic effects of the in situ formed MgS, Ni and Mg 2 Ni multiple-phase catalysts during the hydrogenation/dehydrogenation process, the porthole effects for the volume expansion and microstrain of the phase transformation of Mg 2 Ni and Mg 2 NiH 4 and the reduced hydrogen diffusion distance caused by nanosized Mg. This novel method of in situ producing multiple-phase catalysts gives a new horizon for designing high performance hydrogen storage material.

Conversion efficiency in the shrimp, Metapenaeus monoceros (Fabricius), fed on decomposed mangrove leaves

Digital Repository Service at National Institute of Oceanography (India)

Sumitra-Vijayaraghavan; Ramadhas, V.

Feeding experiments were carried out with Metapenaeus monoceros using mangrove leaves at different stages of decomposition, in combination with rice bran. Maximum conversion efficiency was found in shrimps fed completely decomposed mangrove leaves...

Generalized Schmidt decomposability and its relation to projective norms in multipartite entanglement

International Nuclear Information System (INIS)

Sokoli, Florian; Alber, Gernot

2014-01-01

Projective norms are capable of measuring entanglement of multipartite quantum states. However, typically, the explicit computation of these distance-based geometric entanglement monotones is very difficult even for finite dimensional systems. Motivated by the significance of Schmidt decompositions for our quantitative understanding of bipartite quantum entanglement, a generalization of this concept to multipartite scenarios is proposed, in the sense that generalized Schmidt decomposability of a multipartite pure state implies that its projective norm can be calculated in a simple way analogous to the bipartite case. Thus, this concept of generalized Schmidt decomposability of multipartite quantum states is linked in a natural way to projective norms as entanglement monotones. Therefore, it may not only be a convenient tool for calculations, but may also shed new light onto the intricate features of multipartite entanglement in an analogous way as the ‘classical’ Schmidt decomposition does for bipartite quantum systems. (paper)

Rhodium-catalyzed triarylphosphine synthesis via cross-coupling of aryl iodides and acylphosphines

Directory of Open Access Journals (Sweden)

Jiefang Yang

2018-01-01

Full Text Available Rhodium(I-catalyzed C–P cross-coupling reaction with aryl iodides and acylphosphines was disclosed for a straight forward synthesis of triarylphosphines. The acylphosphines were successfully employed as both the phosphorus source and the ligand to the Rh(I catalyst. The triarylphosphines could be afforded in a yield up to 98% with good toleration of wide functional groups.

Iodide and iodate sodalites for the long-term storage of iodine-129

International Nuclear Information System (INIS)

Strachan, D.M.; Babad, H.

1979-01-01

There exist several proposals for the storage of 129 I. None of these propose the use of a mineral with demonstrated geologic stability. The work described in this paper has identified the minerals iodide and iodate sodalites [Na 8 (AlSiO 4 ) 6 I 2 /(IO 3 ) 2 ] as good candidates for the long-term storage of 129 I. 4 tables

Analytic study of the chain dark decomposition reaction of iodides - atomic iodine donors - in the active medium of a pulsed chemical oxygen-iodine laser: 1. Criteria for the development of the branching chain dark decomposition reaction of iodides

International Nuclear Information System (INIS)

Andreeva, Tamara L; Kuznetsova, S V; Maslov, Aleksandr I; Sorokin, Vadim N

2009-01-01

The scheme of chemical processes proceeding in the active medium of a pulsed chemical oxygen-iodine laser (COIL) is analysed. Based on the analysis performed, the complete system of differential equations corresponding to this scheme is replaced by a simplified system of equations describing in dimensionless variables the chain dark decomposition of iodides - atomic iodine donors, in the COIL active medium. The procedure solving this system is described, the basic parameters determining the development of the chain reaction are found and its specific time intervals are determined. The initial stage of the reaction is analysed and criteria for the development of the branching chain decomposition reaction of iodide in the COIL active medium are determined. (active media)

Numerical analysis on effect of aspect ratio of planar solid oxide fuel cell fueled with decomposed ammonia

Science.gov (United States)

Tan, Wee Choon; Iwai, Hiroshi; Kishimoto, Masashi; Brus, Grzegorz; Szmyd, Janusz S.; Yoshida, Hideo

2018-04-01

Planar solid oxide fuel cells (SOFCs) with decomposed ammonia are numerically studied to investigate the effect of the cell aspect ratio. The ammonia decomposer is assumed to be located next to the SOFCs, and the heat required for the endothermic decomposition reaction is supplied by the thermal radiation from the SOFCs. Cells with aspect ratios (ratios of the streamwise length to the spanwise width) between 0.130 and 7.68 are provided with the reactants at a constant mass flow rate. A parametric study is conducted by varying the cell temperature and fuel utility factor to investigate their effects on the cell performance in terms of the voltage efficiency. The effect of the heat supply to the ammonia decomposer is also studied. The developed model shows good agreement, in terms of the current-voltage curve, with the experimental data obtained from a short stack without parameter tuning. The simulation study reveals that the cell with the highest aspect ratio achieves the highest performance under furnace operation. On the other hand, the 0.750 aspect ratio cell with the highest voltage efficiency of 0.67 is capable of thermally sustaining the ammonia decomposers at a fuel utility of 0.80 using the thermal radiation from both sidewalls.

Rating Migration and Bond Valuation: Decomposing Rating Migration Matrices from Market Data via Default Probability Term Structures

Directory of Open Access Journals (Sweden)

Brian BARNARD

2017-09-01

Full Text Available The study builds on previous research that decomposes rating category default probability term structures from rating category interest rate term structures, and proposes a method to decompose rating migration matrices from market data, via decomposed default probability term structures. To investigate the power and accuracy of the proposed method, it was examined to what extent an existing, known rating migration matrix could again be surfaced by the method. Overall, the results are more than satisfactory, and the method promises to be accurate. Although not considered here, the main objective is the application of the method to market data. The outcome should be insightful in itself, and can be used to evaluate historical rating migration matrices commonly devised by rating agencies, and to form a better understanding of the default probability term structures embedded in market data.

Temperature dependent energy levels of methylammonium lead iodide perovskite

Science.gov (United States)

Foley, Benjamin J.; Marlowe, Daniel L.; Sun, Keye; Saidi, Wissam A.; Scudiero, Louis; Gupta, Mool C.; Choi, Joshua J.

2015-06-01

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.

Crystal growth and applications of mercuric iodide. Report S-242-TP

International Nuclear Information System (INIS)

Schieber, M.; Roth, M.; Schnepple, W.F.

1983-01-01

A brief summary is given of a paper which discusses the crystal growth of mercuric iodide, a high-Z wide bandgap semiconductor suitable as a low noise, room temperature x-ray and gamma-ray detector. The paper summarized also reviews the state-of-the-art of the synthesis and purification of the starting material, mechanical properties and dislocation structure of HgI 2 , and recent success in the development of thick HgI 2 spectrometers

Leaching of Au, Ag, and Pd from waste printed circuit boards of mobile phone by iodide lixiviant after supercritical water pre-treatment

International Nuclear Information System (INIS)

Xiu, Fu-Rong; Qi, Yingying; Zhang, Fu-Shen

2015-01-01

Highlights: • We report a novel process for recovering Au, Ag, and Pd from waste PCBs. • The effect of SCWO on the leaching of Au, Ag, and Pd in waste PCBs was studied. • SCWO was highly efficient for enhancing the leaching of Au, Ag, and Pd. • The optimum leaching parameters for Au, Ag, and Pd in iodine–iodide were studied. - Abstract: Precious metals are the most attractive resources in waste printed circuit boards (PCBs) of mobile phones. In this work, an alternative process for recovering Au, Ag, and Pd from waste PCBs of mobile phones by supercritical water oxidation (SCWO) pre-treatment combined with iodine–iodide leaching process was developed. In the process, the waste PCBs of mobile phones were pre-treated in supercritical water, then a diluted hydrochloric acid leaching (HL) process was used to recovery the Cu, whose leaching efficiency was approximately 100%, finally the resulting residue was subjected to the iodine–iodide leaching process for recovering the Au, Ag, and Pd. Experimental results indicated that SCWO pre-treatment temperature, time, and pressure had significant influence on the Au, Ag, and Pd leaching from (SCWO + HL)-treated waste PCBs. The optimal SCWO pre-treatment conditions were 420 °C and 60 min for Au and Pd, and 410 °C and 30 min for Ag. The optimum dissolution parameters for Au, Pd, and Ag in (SCWO + HL)-treated PCBs with iodine–iodide system were leaching time of 120 min (90 min for Ag), iodine/iodide mole ratio of 1:5 (1:6 for Ag), solid-to-liquid ratio (S/L) of 1:10 g/mL (1:8 g/mL for Ag), and pH of 9, respectively. It is believed that the process developed in this study is environment friendly for the recovery of Au, Ag, and Pd from waste PCBs of mobile phones by SCWO pre-treatment combined with iodine–iodide leaching process

Leaching of Au, Ag, and Pd from waste printed circuit boards of mobile phone by iodide lixiviant after supercritical water pre-treatment

Energy Technology Data Exchange (ETDEWEB)

Xiu, Fu-Rong, E-mail: xiu_chem@hotmail.com [College of Ecological Environment and Urban Construction, Fujian University of Technology, Fuzhou 350108 (China); Qi, Yingying [College of Ecological Environment and Urban Construction, Fujian University of Technology, Fuzhou 350108 (China); Zhang, Fu-Shen [Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China)

2015-07-15

Highlights: • We report a novel process for recovering Au, Ag, and Pd from waste PCBs. • The effect of SCWO on the leaching of Au, Ag, and Pd in waste PCBs was studied. • SCWO was highly efficient for enhancing the leaching of Au, Ag, and Pd. • The optimum leaching parameters for Au, Ag, and Pd in iodine–iodide were studied. - Abstract: Precious metals are the most attractive resources in waste printed circuit boards (PCBs) of mobile phones. In this work, an alternative process for recovering Au, Ag, and Pd from waste PCBs of mobile phones by supercritical water oxidation (SCWO) pre-treatment combined with iodine–iodide leaching process was developed. In the process, the waste PCBs of mobile phones were pre-treated in supercritical water, then a diluted hydrochloric acid leaching (HL) process was used to recovery the Cu, whose leaching efficiency was approximately 100%, finally the resulting residue was subjected to the iodine–iodide leaching process for recovering the Au, Ag, and Pd. Experimental results indicated that SCWO pre-treatment temperature, time, and pressure had significant influence on the Au, Ag, and Pd leaching from (SCWO + HL)-treated waste PCBs. The optimal SCWO pre-treatment conditions were 420 °C and 60 min for Au and Pd, and 410 °C and 30 min for Ag. The optimum dissolution parameters for Au, Pd, and Ag in (SCWO + HL)-treated PCBs with iodine–iodide system were leaching time of 120 min (90 min for Ag), iodine/iodide mole ratio of 1:5 (1:6 for Ag), solid-to-liquid ratio (S/L) of 1:10 g/mL (1:8 g/mL for Ag), and pH of 9, respectively. It is believed that the process developed in this study is environment friendly for the recovery of Au, Ag, and Pd from waste PCBs of mobile phones by SCWO pre-treatment combined with iodine–iodide leaching process.

Decomposing Cross-Country Differences in Skills:

DEFF Research Database (Denmark)

Albæk, Karsten; Rosdahl, Anders

2017-01-01

This paper performs multivariate analysis of skill differences in the Nordic countries as assessed by OECD’s PIACC survey of adults aged 16-65. We decompose the differences in average skills between Finland and each of the three Scandinavian countries into a component that is due to different skill...... levels in subgroups of the population and a component that is due to differences in the composition of subgroups. The decompositions show that the high Finnish average skill level compared to the three Scandinavian countries can be attributed the low share of immigrants in Finland and to high scores...... among Finns with high school and less than high school education. The Finnish average score is pulled substantially downwards as a consequence of the low numeracy skill level among older Finns, which is consistent with an increase in the quantity or quality of Finnish education over time, relative...

Ab initio calculation of transport properties between PbSe quantum dots facets with iodide ligands

Science.gov (United States)

Wang, B.; Patterson, R.; Chen, W.; Zhang, Z.; Yang, J.; Huang, S.; Shrestha, S.; Conibeer, G.

2018-01-01

The transport properties between Lead Selenide (PbSe) quantum dots decorated with iodide ligands has been studied using density functional theory (DFT). Quantum conductance at each selected energy levels has been calculated along with total density of states and projected density of states. The DFT calculation is carried on using a grid-based planar augmented wave (GPAW) code incorporated with the linear combination of atomic orbital (LCAO) mode and Perdew Burke Ernzerhof (PBE) exchange-correlation functional. Three iodide ligand attached low index facets including (001), (011), (111) are investigated in this work. P-orbital of iodide ligand majorly contributes to density of state (DOS) at near top valence band resulting a significant quantum conductance, whereas DOS of Pb p-orbital shows minor influence. Various values of quantum conductance observed along different planes are possibly reasoned from a combined effect electrical field over topmost surface and total distance between adjacent facets. Ligands attached to (001) and (011) planes possess similar bond length whereas it is significantly shortened in (111) plane, whereas transport between (011) has an overall low value due to newly formed electric field. On the other hand, (111) plane with a net surface dipole perpendicular to surface layers leading to stronger electron coupling suggests an apparent increase of transport probability. Apart from previously mentioned, the maximum transport energy levels located several eVs (1 2 eVs) from the edge of valence band top.

Continuous realtime radioiodine monitor employing on-line methyl iodide conversion

International Nuclear Information System (INIS)

Fernandez, S.J.; Motes, B.G.

1980-01-01

An integrated 14 C, 129 I, and 85 Kr monitor was proposed by Fernandez, et al. that separates 129 I from 85 Kr by selective permeation across thin silicone rubber membranes. Subsequent studies of the permeation of CH 3 I and I 2 through silicone rubber membranes demonstrated that I 2 transport across the membranes is too slow to be useful in a realtime monitor. Transport of methyl iodide, however, is rapid and gives a separation factor of greater than 100 from 85 Kr

Reactions of butadiyne. 1: The reaction with hydrogen atoms

Science.gov (United States)

Schwanebeck, W.; Warnatz, J.

1984-01-01

The reaction of hydrogen (H) atoms with butadiene (C4H2) was studied at room temperature in a pressure range between w mbar and 10 mbar. The primary step was an addition of H to C4H2 which is in its high pressure range at p 1 mbar. Under these conditions the following addition of a second H atom lies in the transition region between low and high pressure range. Vibrationally excited C4H4 can be deactivated to form buten-(1)-yne-(3)(C4H4) or decomposes into two C2H2 molecules. The rate constant at room temperature for primary step is given. The second order rate constant for the consumption of buten-(1)-yne-(3) is an H atom excess at room temperature is given.

The Role of Connectivity on Electronic Properties of Lead Iodide Perovskite-Derived Compounds

NARCIS (Netherlands)

Kamminga, Machteld E; De Wijs, Gilles; Havenith, Remco W A; Blake, Graeme R; Palstra, Thomas T M

2017-01-01

We use a layered solution crystal growth method to synthesize high-quality single crystals of two different benzylammonium lead iodide perovskite-like organic/inorganic hybrids. The well-known (C6H5CH2NH3)(2)PbI4 phase is obtained in the form of bright orange platelets, with a structure comprised of

Radiation treatment of organic substances which are difficult to decompose for utilizing sewage water again. Radiation decomposition of lignin

International Nuclear Information System (INIS)

Sekiguchi, Masayuki; Sawai, Taruko; Tanabe, Hiroko

1996-01-01

The sewerage model projects utilizing sewage-treated water and the sewerage model project for the future city executed in Tokyo are described. It is important to obtain the treated water which is suitable to purposes by setting up the target for control and reducing the organic contamination which is difficult to decompose. In fiscal year 1995, as to the decomposing treatment of lignin by radiation, the effect of reducing coloring and the influence when actual flowing-in sewage and treated water coexist were examined. The experimental samples were lignin aqueous solution, synthetic sewage and flowing-in sewage, treated water, and the mixture of treated water and synthetic sewage. The measurement of water quality is explained. The γ ray irradiation with a Co-60 source was carried out. The results of respective samples are reported. When total organic carbon was at the level in flowing-in sewage and treated water, irradiation was effective for eliminating coloring. The soluble organic substances which are difficult to decompose were efficiently decomposed by irradiation. (K.I.)

The possession of brochures on emergency and of iodide tablets by households

International Nuclear Information System (INIS)

Hultaaker, Oe.

1985-01-01

People who live within twelve to fifteen kilometers from one of the Swedish Nuclear Power plants have received a brochure about existing security arrangements and the actions which they are recommended to take in the wake of a nuclear accident. Tablets containing potassium iodide have also been handed out to the people living close to the power plants. Due to the short life of the iodide tablets, people receive new ones from time to time. Before the distribution of new tablets, however, the National Institute of Radiation Protection wanted to learn if people still had the old tablets and the brochure in their homes. The National Institute of Radiation Protection also was interested in assessing people's knowledge about the protection given by the iodide tablets and whether people knew when to take them. Nine persons out of ten (87%) could show the tablets to the interviewers, and seven out of ten (71%) could do so with the brochure. Half of the total number of respondents knew when they were supposed to take the tablets (47%). Nevertheless two partly conflicting messages have been given to the public about the proper time to take the tablet: according to the text printed on the cover of the tablets, they are to be taken immediately when the people have learnt about an accident; but according to the brochure distributed to the households, people must wait until they are told by the radio to take the tablets. One person of four (22%) said that the radio should inform them, and almost the same number of people (25%) said that the tablets ought to be taken immediately following an accident. Only one person of four (27%) knew what protection they would get from the iodine tablets. Another 17% had a vague idea about the affect resulting from taking them. Many people (25%) had the false belief that the tablets offered them general protection against radiation. (author)

[The inhibitory effect of decomposed Chinese traditional medicine Chaihu on Coxsackie B virus(CVB3m) replication and its influence on cell activity].

Science.gov (United States)

Wang, X; Wang, Y; Liu, F; Wei, K L

2001-09-01

To study the anti-Coxsackie B virus (CVB3m) action of Chaihu(XCT) and its decomposed herb soups No.1 and No.2 in vitro, and also their protective effect on cells. The anti CVB3m and cell protection effects of XCT and its decomposed herb soups No.1 and No.2 were observed by the methods of micro-cell culture and neutral red ingestion, taking cytopathic effect and cell activity as judgments of medicine toxicity and virus replication. The non-toxic concentrations of XCTand its decomposed herb soups No.1 and No.2 had no apparent influence on HeLa cell activity, on the contrary, in certain range of concentrations, they could promote cell growth and cell activity. In therapeutic cell group, XCT and its decomposed herb soups No.1 and No.2 all had apparent inhibitory effect on CVB3m replication, especially the decomposed No.1 showing an inhibitory rate of 107.6%. Under the same decomposed No.1 concentration(1.5 mg/ml), the viral inhibitory rate of the preventive therapeutic cell group was much higher than that of the therapeutic cell group, reaching as high as 128.1%. In virus adsorbed cell group, the CVB3m was also obviously inhibited by the XCT and decomposed No.1 and No.2. By comparing the effects on cell protection and virus replication of XCT and its decomposed herb soups No.1 and No.2, it identifies that XCT can protect cells against virus infection and directly kill the CVB3m, this Chinese herb medicine may be applied clinically for preventing and curing of viral myocarditis.

Four wind speed multi-step forecasting models using extreme learning machines and signal decomposing algorithms

International Nuclear Information System (INIS)

Liu, Hui; Tian, Hong-qi; Li, Yan-fei

2015-01-01

Highlights: • A hybrid architecture is proposed for the wind speed forecasting. • Four algorithms are used for the wind speed multi-scale decomposition. • The extreme learning machines are employed for the wind speed forecasting. • All the proposed hybrid models can generate the accurate results. - Abstract: Realization of accurate wind speed forecasting is important to guarantee the safety of wind power utilization. In this paper, a new hybrid forecasting architecture is proposed to realize the wind speed accurate forecasting. In this architecture, four different hybrid models are presented by combining four signal decomposing algorithms (e.g., Wavelet Decomposition/Wavelet Packet Decomposition/Empirical Mode Decomposition/Fast Ensemble Empirical Mode Decomposition) and Extreme Learning Machines. The originality of the study is to investigate the promoted percentages of the Extreme Learning Machines by those mainstream signal decomposing algorithms in the multiple step wind speed forecasting. The results of two forecasting experiments indicate that: (1) the method of Extreme Learning Machines is suitable for the wind speed forecasting; (2) by utilizing the decomposing algorithms, all the proposed hybrid algorithms have better performance than the single Extreme Learning Machines; (3) in the comparisons of the decomposing algorithms in the proposed hybrid architecture, the Fast Ensemble Empirical Mode Decomposition has the best performance in the three-step forecasting results while the Wavelet Packet Decomposition has the best performance in the one and two step forecasting results. At the same time, the Wavelet Packet Decomposition and the Fast Ensemble Empirical Mode Decomposition are better than the Wavelet Decomposition and the Empirical Mode Decomposition in all the step predictions, respectively; and (4) the proposed algorithms are effective in the wind speed accurate predictions

Decomposing a planar graph into an independent set and a 3-degenerate graph

DEFF Research Database (Denmark)

Thomassen, Carsten

2001-01-01

We prove the conjecture made by O. V. Borodin in 1976 that the vertex set of every planar graph can be decomposed into an independent set and a set inducing a 3-degenerate graph. (C) 2001 Academic Press....

Excellent Silicon Surface Passivation Achieved by Industrial Inductively Coupled Plasma Deposited Hydrogenated Intrinsic Amorphous Silicon Suboxide

Directory of Open Access Journals (Sweden)

Jia Ge

2014-01-01

Full Text Available We present an alternative method of depositing a high-quality passivation film for heterojunction silicon wafer solar cells, in this paper. The deposition of hydrogenated intrinsic amorphous silicon suboxide is accomplished by decomposing hydrogen, silane, and carbon dioxide in an industrial remote inductively coupled plasma platform. Through the investigation on CO2 partial pressure and process temperature, excellent surface passivation quality and optical properties are achieved. It is found that the hydrogen content in the film is much higher than what is commonly reported in intrinsic amorphous silicon due to oxygen incorporation. The observed slow depletion of hydrogen with increasing temperature greatly enhances its process window as well. The effective lifetime of symmetrically passivated samples under the optimal condition exceeds 4.7 ms on planar n-type Czochralski silicon wafers with a resistivity of 1 Ωcm, which is equivalent to an effective surface recombination velocity of less than 1.7 cms−1 and an implied open-circuit voltage (Voc of 741 mV. A comparison with several high quality passivation schemes for solar cells reveals that the developed inductively coupled plasma deposited films show excellent passivation quality. The excellent optical property and resistance to degradation make it an excellent substitute for industrial heterojunction silicon solar cell production.

Rich Dad, Smart Dad: Decomposing the Intergenerational Transmission of Income

OpenAIRE

Lefgren, Lars; Lindquist, Matthew; Sims, David

2009-01-01

We construct a simple model, consistent with Becker and Tomes (1979), that decomposes the intergenerational income elasticity into the causal effect of financial resources, the mechanistic transmission of human capital, and the role that human capital plays in the determination of father’s permanent income. We show how a particular set of instrumental variables could separately identify the money and human capital transmission effects. We further outline two instrumental variables methods for...

Decomposing interactions using GLM in combination with the COMPARE, LMATRIX and MMATRIX subcommands in SPSS

Directory of Open Access Journals (Sweden)

Glen T. Howell

2012-02-01

Full Text Available In this tutorial, we provide researchers who use SPSS step-by-step instructions for decomposing interactions when a three-way ANOVA is conducted using the GLM procedure. We start with a demonstration of how a two-way interaction can be decomposed using the COMPARE subcommand in combination with syntax. Then, we provide instructions with examples for conducting simple interaction and second-order simple effects analyses for three-way ANOVAs with between-subjects, within-subjects, and mixed between- and within-subjects variables using the LMATRIX or MMATRIX subcommands. Provided in Appendices are general rules that can be used to derive design-specific LMATRIX and MMATRIX subcommands.

Leaching of Au, Ag, and Pd from waste printed circuit boards of mobile phone by iodide lixiviant after supercritical water pre-treatment.

Science.gov (United States)

Xiu, Fu-Rong; Qi, Yingying; Zhang, Fu-Shen

2015-07-01

Precious metals are the most attractive resources in waste printed circuit boards (PCBs) of mobile phones. In this work, an alternative process for recovering Au, Ag, and Pd from waste PCBs of mobile phones by supercritical water oxidation (SCWO) pre-treatment combined with iodine-iodide leaching process was developed. In the process, the waste PCBs of mobile phones were pre-treated in supercritical water, then a diluted hydrochloric acid leaching (HL) process was used to recovery the Cu, whose leaching efficiency was approximately 100%, finally the resulting residue was subjected to the iodine-iodide leaching process for recovering the Au, Ag, and Pd. Experimental results indicated that SCWO pre-treatment temperature, time, and pressure had significant influence on the Au, Ag, and Pd leaching from (SCWO+HL)-treated waste PCBs. The optimal SCWO pre-treatment conditions were 420°C and 60min for Au and Pd, and 410°C and 30min for Ag. The optimum dissolution parameters for Au, Pd, and Ag in (SCWO+HL)-treated PCBs with iodine-iodide system were leaching time of 120min (90min for Ag), iodine/iodide mole ratio of 1:5 (1:6 for Ag), solid-to-liquid ratio (S/L) of 1:10g/mL (1:8g/mL for Ag), and pH of 9, respectively. It is believed that the process developed in this study is environment friendly for the recovery of Au, Ag, and Pd from waste PCBs of mobile phones by SCWO pre-treatment combined with iodine-iodide leaching process. Copyright © 2015 Elsevier Ltd. All rights reserved.

Study of hydrogenation of Sm{sub 2}Fe{sub 17-y}Ga{sub y} by means of X-ray diffraction

Energy Technology Data Exchange (ETDEWEB)

Teresiak, A.; Uhlemann, M.; Kubis, M.; Gebel, B.; Mattern, N.; Mueller, K.-H. [Institut fuer Festkoerper- und Werkstofforschung Dresden e.V. (Germany)

2000-06-06

The hydrogenation process of Sm{sub 2}Fe{sub 17-y}Ga{sub y}(y=0-2) was studied. X-ray investigations show a decreasing hydrogen solubility in the intermetallic alloy with increasing Ga-content from 4.0{+-}0.3 atoms per formula unit for Sm{sub 2}Fe{sub 17} to 2.85{+-}0.05 for Sm{sub 2}Fe{sub 15}Ga{sub 2}. The larger Ga atoms reduce the size of the interstitial sites and thereby the maximum hydrogen concentration is decreased. The behaviour of the lattice parameters a and c with increasing Ga content points to a changed hydrogen distribution on the interstitial sites, becoming more statistical. In situ observations by means of high temperature X-ray diffraction show that the hydrogen absorption process is diffusion controlled. The hydrogen absorption starts at an annealing temperature of 120-140 C in all cases. The solubility of hydrogen decreases with increasing temperature. The hydrogen is completely desorbed above 350 C in all cases. The absorption/desorption process is reversible between room temperature and 400 C. Annealing at temperatures above 400 C leads to the decomposition of the Sm{sub 2}Fe{sub 17} phase, indicated by emerging of {alpha}-Fe. The formation of SmH{sub x} is established at 600 C. The decomposition temperature increases with increasing Ga-content. Up to 750 C, only Sm{sub 2}Fe{sub 17} is completely decomposed. (orig.)

Decomposability and mental representation of French verbs.

Science.gov (United States)

Estivalet, Gustavo L; Meunier, Fanny E

2015-01-01

In French, regardless of stem regularity, inflectional verbal suffixes are extremely regular and paradigmatic. Considering the complexity of the French verbal system, we argue that all French verbs are polymorphemic forms that are decomposed during visual recognition independently of their stem regularity. We conducted a behavioral experiment in which we manipulated the surface and cumulative frequencies of verbal inflected forms and asked participants to perform a visual lexical decision task. We tested four types of verbs with respect to their stem variants: a. fully regular (parler "to speak," [parl-]); b. phonological change e/E verbs with orthographic markers (répéter "to repeat," [répét-] and [répèt-]); c. phonological change o/O verbs without orthographic markers (adorer "to adore," [ador-] and [adOr-]); and d. idiosyncratic (boire "to drink," [boi-] and [buv-]). For each type of verb, we contrasted four conditions, forms with high and low surface frequencies and forms with high and low cumulative frequencies. Our results showed a significant cumulative frequency effect for the fully regular and idiosyncratic verbs, indicating that different stems within idiosyncratic verbs (such as [boi-] and [buv-]) have distinct representations in the mental lexicon as different fully regular verbs. For the phonological change verbs, we found a significant cumulative frequency effect only when considering the two forms of the stem together ([répét-] and [répèt-]), suggesting that they share a single abstract and under specified phonological representation. Our results also revealed a significant surface frequency effect for all types of verbs, which may reflect the recombination of the stem lexical representation with the functional information of the suffixes. Overall, these results indicate that all inflected verbal forms in French are decomposed during visual recognition and that this process could be due to the regularities of the French inflectional verbal

Decomposability and mental representation of French verbs

Directory of Open Access Journals (Sweden)

Gustavo Lopez Estivalet

2015-01-01

Full Text Available In French, regardless of stem regularity, inflectional verbal suffixes are extremely regular and paradigmatic. Considering the complexity of the French verbal system, we argue that all French verbs are polymorphemic forms that are decomposed during visual recognition independently of their stem regularity. We conducted a behavioural experiment in which we manipulated the surface and cumulative frequencies of verbal inflected forms and asked participants to perform a visual lexical decision task. We tested four types of verbs with respect to their stem variants: a. fully regular (parler ‘to speak’, [parl-]; b. phonological change e/E verbs with orthographic markers (répéter ‘to repeat’, [répét-] and [répèt-]; c. phonological change o/O verbs without orthographic markers (adorer ‘to adore’, [ador-] and [adOr-]; and d. idiosyncratic (boire ‘to drink’, [boi-] and [buv-]. For each type of verb, we contrasted four conditions, forms with high and low surface frequencies and forms with high and low cumulative frequencies. Our results showed a significant cumulative frequency effect for the fully regular and idiosyncratic verbs, indicating that different stems within idiosyncratic verbs (such as [boi-] and [buv-] have distinct representations in the mental lexicon as different fully regular verbs. For the phonological change verbs, we found a significant cumulative frequency effect only when considering the two forms of the stem together ([répét-] and [répèt-], suggesting that they share a single abstract and underspecified phonological representation. Our results also revealed a significant surface frequency effect for all types of verbs, which may reflect the recombination of the stem lexical representation with the functional information of the suffixes. Overall, these results indicate that all inflected verbal forms in French are decomposed during visual recognition and that this process could be due to the regularities of

Solvent effect on the rate and equilibrium of reaction between 10-phenylphenoxarsine and methyl iodide. Vliyanie rastvoritelya na skorost' i ravnovesie reaktsii 10-fenilfenoksarsina s iodistym metilom

Energy Technology Data Exchange (ETDEWEB)

Gavrilov, V I; Gumerov, N S; Rakhmatullin, R R [Kazanskij Khimiko-Tekhnologicheskij Inst., Kazan (USSR)

1990-02-01

Effect of solvent nature on nucleophilic capacity of three-coordinated arsenic and the equilibrium state of 10-phenylphenoxarsine (PA) reaction with methyl iodide are studied. Kinetic investigations are carried out by the conductometry at 24,35,45 deg C. It is established that quaternization of PA with methyl iodide when substituting a solvent (ketone for alcohol) increases 3-14 times with simultaneous growth of the activation energy value. When transforming from aprotic solvents to protic ones PA interaction equilibrium with methyl iodide shifts to the side of arsonic salt formation.

Achievement report for fiscal 2000 on the phase II research and development for hydrogen utilizing international clean energy system technology (WE-NET). Task 7. Development of hydrogen refueling station; 2000 nendo suiso riyo kokusai clean energy system gijutsu (WE-NET) dai 2 ki kenkyu kaihatsu. Task 7. Suiso kyokyu station no kaihatsu

Energy Technology Data Exchange (ETDEWEB)

NONE

2001-03-01

This paper describes the achievements in fiscal 2000 from the development of hydrogen refueling stand-alone stations for hydrogen fueled automobiles in the WE-NET. Supply capacity of practical size of 1/10, 30 Nm{sup 3} was selected as the object. For the natural gas reformed type hydrogen generator, discussions were given on design and manufacture of a reforming unit and a PSA device. The PCT diagram method was discussed to estimate the capacity of a hydrogen absorbing alloy type storing facility. Interface between fuel cell driven automobiles and the station was adjusted. For the solid polymer electrolyte water decomposition type, safety measures were discussed with a high-pressure filling system kept in mind. Detailed design was made on a water decomposing hydrogen generator. Fabrication was completed on the hydrogen absorbing alloy type storing facility, and verifications were given on the storage amount, hydrogen absorbing speed, and discharge capability. In the high-pressure refueling system, temperature rise was simulated at a pressure of 35 MPa. Refueling for ten minutes raised the gas temperature by 75 degrees C, and the container surface by 65 degrees C. Local temperature rise was forecasted in the actual work, which is a future discussion assignment. An outline method was discussed for the verification test. (NEDO)

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.

Functionalized metal organic frameworks for effective capture of radioactive organic iodides

KAUST Repository

Li, Baiyan

2017-06-27

Highly efficient capture of radioactive organic iodides (ROIs) from off-gas mixtures remains a substantial challenge for nuclear waste treatment. Current materials utilized for ROI sequestration suffer from low capacity, high cost (e.g. use of noble metals), and poor recyclability. Recently, we have developed a new strategy to tackle this challenge by functionalizing MOF materials with tertiary amines to create molecular traps for the effective capture and removal of ROIs (e.g. radioactive methyl iodide) from nuclear wastes. To further enhance the uptake capacity and performance of CH3I capture by ROI molecular traps, herein, we carry out a systematic study to investigate the effect of different amine molecules on ROI capture. The results demonstrate a record-high CH3I saturation uptake capacity of 80% for MIL-101-Cr-DMEDA at 150 °C, which is 5.3 times that of Ag0@MOR (15 wt%), a leading adsorbent material for capturing ROIs during nuclear fuel reprocessing. Furthermore, the CH3I decontamination factors (DFs) for MIL-101-Cr-DMEDA are as high as 5000 under simulated reprocessing conditions, largely exceeding that of facility regulatory requirements (DF = 3000). In addition, MIL-101-Cr-DMEDA can be recycled without loss of capacity, illustrating yet another advantage compared to known industrial adsorbents, which are typically of a

Potassium iodide as a thyroid blocker--Three Mile Island to today

International Nuclear Information System (INIS)

Halperin, J.A.

1989-01-01

The Three Mile Island (TMI) nuclear emergency in the U.S. in March 1979 marked the first occasion when use of potassium iodide (KI) was considered for thyroid blocking of the population in the vicinity of a potentially serious release of fission products from a nuclear power reactor. In face of a demand that could not be satisfied by commercial supplies of low-dose KI drug products from the U.S. pharmaceutical industry, the Food and Drug Administration directed the manufacture and stockpiling of sufficient quantities of saturated solution of potassium iodide (SSKI) to provide protection for one million people in the event of a large-scale release of radioiodines. Although the drug was not used, the experience of producing, stockpiling, and making ready for use a large quantity of the drug resulted in significant public policy, regulatory, and logistical issues. A number of these issues have been resolved through scientific debate and consensus, development of official guidance regarding the proper role of KI in nuclear emergencies, and the approval of New Drug Applications for KI products specifically intended for thyroid blocking in nuclear emergencies. Other issues regarding broad-scale implementation of the guidelines remain today. This paper traces the history of the development and implementation of the use of KI from pre-TMI to the present

Potassium iodide as a thyroid blocker--Three Mile Island to today.

Science.gov (United States)

Halperin, J A

1989-05-01

The Three Mile Island (TMI) nuclear emergency in the U.S. in March 1979 marked the first occasion when use of potassium iodide (KI) was considered for thyroid blocking of the population in the vicinity of a potentially serious release of fission products from a nuclear power reactor. In face of a demand that could not be satisfied by commercial supplies of low-dose KI drug products from the U.S. pharmaceutical industry, the Food and Drug Administration directed the manufacture and stockpiling of sufficient quantities of saturated solution of potassium iodide (SSKI) to provide protection for one million people in the event of a large-scale release of radioiodines. Although the drug was not used, the experience of producing, stockpiling, and making ready for use a large quantity of the drug resulted in significant public policy, regulatory, and logistical issues. A number of these issues have been resolved through scientific debate and consensus, development of official guidance regarding the proper role of KI in nuclear emergencies, and the approval of New Drug Applications for KI products specifically intended for thyroid blocking in nuclear emergencies. Other issues regarding broad-scale implementation of the guidelines remain today. This paper traces the history of the development and implementation of the use of KI from pre-TMI to the present.

Process for the exchange of hydrogen isotopes between streams of liquid water and gaseous halohydrocarbon and an apparatus therefor

International Nuclear Information System (INIS)

Symons, E.A.; Rolston, J.H.; Clermont, M.J.; Paterson, L.M.

1983-01-01

This invention provides a process for the exchange of hydrogen isotopes between streams of liquid water and gaseous halohydrocarbons comprising: (a) bringing into contact a water stream, a halohydrocarbon stream, and a catalytic porous anion exchange resin so that the isotope-deficient halohydrocarbon stream is enriched; (b) decomposing the halohydrocarbon stream photolytically into two gaseous streams, one enriched and the other deficient; (c) removing as a product the first, enriched stream; and (d) recycling the second stream for enrichment. An apparatus is also provided

Chemical dosimetry using an iodide/iodate aqueous solution: application to the gamma irradiation of blood

Energy Technology Data Exchange (ETDEWEB)

Rahn, Ronald O. E-mail: rahnr@ms.soph.uab.edu

2003-01-01

A method is presented for measuring and verifying the radiation dose in gamma irradiators used for treating blood prior to transfusion. This method employs the iodide/iodate dosimeter (0.6 M iodide, 0.1 M iodate, and 0.01 borate at pH 9.25) which forms triiodide upon exposure to ionizing radiation; for Cs-137 radiation the G value is 14.1. Samples were placed in a canister and irradiated in a conventional blood bank irradiator containing several Cs-137 sources. The following were exposed: (a) nine 1.5 ml plastic tubes containing dosimetry solution taped inside a 250 ml blood bag, which, in turn, was filled with either water or blood, (b) 50 ml plastic syringes containing varying amounts of dosimetry solution, (c) a whole blood bag containing 250 ml of the dosimetry solution. A water phantom was not used during exposure. The absorbance changes at 352 nm due to triiodide formation were used to determine a dose rate, which was on the order of 10 Gy/min ({+-}5%) for all samples measured. This value is consistent with an average time-decayed dose rate for the irradiation volume as determined from the manufacturers calibration of the unit taking into account the heterogeneous nature of the radiation field inside the irradiator and the absence of a water phantom. Because of its sensitivity, ease of operation, and reproducibility, it is suggested that the iodide/iodate dosimetry system be considered for on-site periodic conformation/verification of the radiation dose as part of a quality assurance requirement for blood irradiators.

Chemical dosimetry using an iodide/iodate aqueous solution: application to the gamma irradiation of blood

International Nuclear Information System (INIS)

Rahn, Ronald O.

2003-01-01

A method is presented for measuring and verifying the radiation dose in gamma irradiators used for treating blood prior to transfusion. This method employs the iodide/iodate dosimeter (0.6 M iodide, 0.1 M iodate, and 0.01 borate at pH 9.25) which forms triiodide upon exposure to ionizing radiation; for Cs-137 radiation the G value is 14.1. Samples were placed in a canister and irradiated in a conventional blood bank irradiator containing several Cs-137 sources. The following were exposed: (a) nine 1.5 ml plastic tubes containing dosimetry solution taped inside a 250 ml blood bag, which, in turn, was filled with either water or blood, (b) 50 ml plastic syringes containing varying amounts of dosimetry solution, (c) a whole blood bag containing 250 ml of the dosimetry solution. A water phantom was not used during exposure. The absorbance changes at 352 nm due to triiodide formation were used to determine a dose rate, which was on the order of 10 Gy/min (±5%) for all samples measured. This value is consistent with an average time-decayed dose rate for the irradiation volume as determined from the manufacturers calibration of the unit taking into account the heterogeneous nature of the radiation field inside the irradiator and the absence of a water phantom. Because of its sensitivity, ease of operation, and reproducibility, it is suggested that the iodide/iodate dosimetry system be considered for on-site periodic conformation/verification of the radiation dose as part of a quality assurance requirement for blood irradiators

Effects of decomposing Rhizophora apiculata leaves on larvae of the shrimp Penaeus monodon

NARCIS (Netherlands)

Roijackers, R.M.M.; Nghia, T.T.; Ut, V.N.; Scheffer, M.

2006-01-01

We studied the effects of different concentrations of decomposing Rhizophora apiculata leaves and their leachates on larvae of the shrimp Penaeus monodon under laboratory conditions. Shrimp mortality was highly dependent on the concentration of oxygen in the water, which in turn was strongly

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

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

Introduction to fifth international workshop on mercuric iodide nuclear radiation detectors

International Nuclear Information System (INIS)

Schieber, M.

1982-01-01

Mercuric iodide is a wide bandgap semiconductor, with Eg approx. = 2.14 eV at room temperature. Therefore, HgI 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 2 ; recent progress is reported

Hydrothermal decomposition of TBP and fixation of its decomposed residue by HHP technique

International Nuclear Information System (INIS)

Yamasaki, N.; Fujiki, M.; Nishioka, M.; Ioku, K.; Yanagisawa, K.; Kozai, N.; Muraoka, S.

1991-01-01

The tributyl phosphate (TBP) used for the fuel reprocessing by Purex process is discharged as spent solvent because of the chemical decomposition and the damage due to radiation. Alkaline hydrothermal treatment in oxygen which is the reaction in a closed system is effective for the decomposition of TBP as it can transform organic materials to stable inorganic ions. Hydrothermal hot pressing technique has been applied to the immobilization of various radioactive wastes. This work deals with the continuous treatment process for the decomposition of TBP waste and the immobilization of its decomposed residue under hydrothermal condition. These processes are outlined. The experiment and the results are reported. TBP was completely decomposed above 200degC, and COD value showed the maximum at 250degC. The reaction process consists of two steps of the hydrolysis of TBP and the oxidation of the formed organic material. (K.I.)

Thermally decomposed ricebran oil as a diesel fuel

Directory of Open Access Journals (Sweden)

Megahed, O. A.

1998-04-01

Full Text Available Ricebran oil; a non edible oil, was thermally decomposed using different loads of calcium oxide as catalyst. The fuel properties of the cracked product were evaluated as compared to those of diesel fuel. The considered properties included the calorific value, flash point, viscosity, pour point, distillation characteristics, cetane number in addition to some other fuel properties. The results had shown that the fuel properties of the decomposed oil were quite similar to those of standard diesel fuel. The calorific value was 80-90% that of diesel fuel and the viscosity was sligthy higher. The prepared fuel was advantageous over diesel fuel as the former was completely free from sulfur, which on fuel combustion produces corrosive gases of sulfur oxides.

Aceite de germen de arroz, un aceite no comestible, fue descompuesto térmicamente usando diferentes cantidades de óxido cálcico como catalizador. Las propiedades combustibles del producto craqueado fueron evaluadas comparándolas con las del gasóleo. Las propiedades consideradas incluyeron el poder calorífico, punto de inflamación, viscosidad, temperatura de fluidez crítica, características de destilación, número de cetano y otras propiedades de los combustibles. Los resultados han mostrado que las propiedades combustibles del aceite descompuesto fueron bastantes similares a la de los gasóleos estándar. El poder calorífico fue del 80-90% de la del gasóleo y la viscosidad ligeramente mayor. El combustible preparado fue ventajoso sobre el gasóleo ya que el primero estaba completamente libre de sulfuro, el cual produce en la combustión del carburante gases corrosivos de óxido de azufre.

Parametric study on removal efficiency of impregnated activated charcoal and silver zeolite for radioactive methyl iodide

International Nuclear Information System (INIS)

Shiomi, H.; Yuasa, Y.; Tani, A.; Ohki, M.; Nakagawa, T.

1983-01-01

The removal efficiency of impregnated activated charcoal and silver zeolite for radioactive methyl iodide is influenced by various parameters such as temperature, relative humidity, face velocity and packing density. This study is to evaluate the dependency of the removal efficiency on each parameter and these combined parameters, quantitatively. Four types of adsorbents, BC-727, AgX, CHC-50 and SS 208C 5KI 3 , were tested. From experimental data and mass transfer theory, an experimental equation for evaluating the removal efficiency of adsorbents was derived under a series of experiments for radioactive methyl iodine-131. It was concluded that the removal efficiency calculated from the experimental equation agreed well with the experimental value. Effects of experimental specific parameters, such as Pre-flow time, methyl iodide injection time and After-flow time, on the removal efficiency of adsorbent are also described

Comparative study of decomposable and indecomposable biopsy needle in lung puncture biopsy

International Nuclear Information System (INIS)

Wang Bo; Sheng Zhanxin; Wen Yamin; Zhang Liping; Wen Zongqiu

2007-01-01

Objective: To contrast the clinical practice characteristics with decomposable and indecomposable biopsy needle in the CT-guided lung puncture biopsy. Methods: 50 patients with lung tumour carried on puncture biopsy under the CT guidance were divided in two groups randomly: Group A (25 examples): using the indecomposable BioPinceTM biopsy needle; Group B(25 examples): using the decomposable Precisa or Vitesse biopsy needle. The puncture biopsy organization quantity, the first time puncture success rate, the pathological diagnosis result and the incidence of puncture complication were compared in two groups. Results: More striped structures were gained obviously in group A than in group B: 24/25 and 11/25 respectively (P>0.05), The pathological diagnosis 'serious extrusion amoebocyte and nature undetermined' only occurred in group B. But the first time puncture success rate was lower in group A than in B: 52%(13/25) and 80%(20/25) respectively (P>0.05), The incidence of hemorrhage and pneumothorax in group A was higher slightly: 84% and 72%, 16% and 4% respectively (P>0.05). Conclusion: The indecomposable needle (BioPinceTM) was better in lung puncture biopsy, but the lower first time puncture success rate also increases the risk of operation and complication in some degree because of the structure of the needle. On the contrary, decomposable needle (the Precisa or the Vitesse) was not the best choice in lung puncture biopsy. But it had the original superiority, especially regarding the special patient such as patient with small tumour, thin thoracic wall, bad physique for its nimble operation. It is essential for us to use the two different types of biopsy needle rationally to enhance the level of CT-guided lung puncture biopsy. (authors)

Iodate and iodo-trihalomethane formation during chlorination of iodide-containing waters: role of bromide.

Science.gov (United States)

Criquet, Justine; Allard, Sebastien; Salhi, Elisabeth; Joll, Cynthia A; Heitz, Anna; von Gunten, Urs

2012-07-03

The kinetics of iodate formation is a critical factor in mitigation of the formation of potentially toxic and off flavor causing iodoorganic compounds during chlorination. This study demonstrates that the formation of bromine through the oxidation of bromide by chlorine significantly enhances the oxidation of iodide to iodate in a bromide-catalyzed process. The pH-dependent kinetics revealed species specific rate constants of k(HOBr + IO(-)) = 1.9 × 10(6) M(-1) s(-1), k(BrO(-) + IO(-)) = 1.8 × 10(3) M(-1) s(-1), and k(HOBr + HOI) < 1 M(-1) s(-1). The kinetics and the yield of iodate formation in natural waters depend mainly on the naturally occurring bromide and the type and concentration of dissolved organic matter (DOM). The process of free chlorine exposure followed by ammonia addition revealed that the formation of iodo-trihalomethanes (I-THMs), especially iodoform, was greatly reduced by an increase of free chlorine exposure and an increase of the Br(-)/I(-) ratio. In water from the Great Southern River (with a bromide concentration of 200 μg/L), the relative I-incorporation in I-THMs decreased from 18 to 2% when the free chlorine contact time was increased from 2 to 20 min (chlorine dose of 1 mg Cl(2)/L). This observation is inversely correlated with the conversion of iodide to iodate, which increased from 10 to nearly 90%. Increasing bromide concentration also increased the conversion of iodide to iodate: from 45 to nearly 90% with a bromide concentration of 40 and 200 μg/L, respectively, and a prechlorination time of 20 min, while the I-incorporation in I-THMs decreased from 10 to 2%.

Transfer of the sodium/iodide symporter gene into gliomas for radioiodine therapy in vitro

International Nuclear Information System (INIS)

Tan Jian; Li Wei; Liu Xiaohua; Xiao Qian; Jia Qiang; Li Ning

2008-01-01

Objective: The most frequent brain tumors are the gliomas. Glioblastomas are largely incurable secondary, to their rapid, aggressive and diffusely infiltrative growth pattern and hypervascularity. This study aimed at investigating the possibility of transecting human sodium/iodide symporter (hNIS) gene into human glioma cell lines to facilitate radioactive iodide treatment in vitro. Methods: Transecting hNIS gene into human glioma cell lines U251 was performed by recombinant expression plasmids with lipofectamine 2000-plasmid complexes. The hNIS gene cell lines with stable expression (hNIS-U251) were selected through G418 antibiotic constraint. The hNIS-U251 gene cell lines were then evaluated for their biologic functions, including 125 I uptake assay, 125 I influx-course, 125 I-efflux-course, 131 I inhibitory effect on cellular proliferation by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyhe-trazolium bromide (MTT) assay and flow cytometer. Results: We were successful in transecting hNIS gene into human glioma cell lines by recombinant expression plasmids, and were able to obtain hNIS gene cell lines (hNIS-U251) with stable expression. The hNIS-U251 cell lines could intake and bind radioactive iodide by hNIS gene. The uptakes of 125 I were 117 fold higher in hNIS-U251 cell lines than U251 cell lines [(50 469.88 ± 997.29), (432.92 ± 89.28) counts·min -1 , respectively]. And the proliferation index of hNIS-U251 cell lines was lower than U251 cell lines after incubating with 131 I. Conclusion: The hNIS gene with stable gene expression (hNIS- U251) cell lines could be labeled by 131 I with a high efficiency, thereby may function effectively in the treatment of glioma-related brain tumors. (authors)

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

Characterization of thermally evaporated lead iodide films aimed for the detection of X-rays

International Nuclear Information System (INIS)

Caldeira Filho, A.M.; Mulato, M.

2011-01-01

Some semiconductor materials such as lead iodide (PbI 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 8 Ω 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.