Optical bio-sniffer for methyl mercaptan in halitosis.

Science.gov (United States)

Mitsubayashi, Kohji; Minamide, Takeshi; Otsuka, Kimio; Kudo, Hiroyuki; Saito, Hirokazu

2006-07-28

An optical bio-sniffer for methyl mercaptan (MM) one of major odorous chemicals in halitosis (bad breath) was constructed by immobilizing monoamine oxidase type A (MAO-A) onto a tip of a fiber optic oxygen sensor (od: 1.59 mm) with an oxygen sensitive ruthenium organic complex (excitation: 470 nm, fluorescent: 600 nm). A flow cell for circulating buffer solution was applied to rinse and clean the tip of the device like nasal mucosa. In order to amplify the bio-sniffer output, a substrate regeneration cycle caused by coupling MAO-A with l-ascorbic acid (AsA) as reducing reaction with reagent system was applied to the sensor system. After evaluating the sensor characteristics using a gas flow measurement system with a gas generator, the optical bio-sniffer was applied to expired gases from healthy male volunteers for halitosis analysis as a physiological application. The optical bio-sniffer was applied to detect the oxygen consumption induced by MAO-A enzymatic reaction (and AsA chemical reduction) with gaseous MM application. The bio-sniffer was calibrated against MM vapor from 8.7 to 11500 ppb with correlation coefficient of 0.977, including a MM threshold (200 ppb) of pathologic halitosis and the human sense of smell level 3.5 (10.0 ppb), with good gas-selectivity based on the MAO-A substrate specificity. As the result of the physiological application, the optical bio-sniffer could successfully monitor the MM level change in breath samples during daytime, which is consistent with the previously reported results.

Preparação de fibras de polipropileno modificadas com grupos mercaptan e sua utilização em compósitos com resina epoxídica

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Dutra Rita C. L.

1999-01-01

Full Text Available Fibras de polipropileno modificadas com grupos mercaptan foram desenvolvidas através de processo de extrusão/fiação de misturas contendo PP e EVA modificado com grupos mercaptan (EVASH. A superfície destas fibras foi analisada por espectroscopia foto-eletrônica de raios-X (XPS, espectroscopia no infravermelho com transformada de Fourier, utilizando-se a técnica de refletância difusa (DRIFTS, tensão superficial e microscopia eletrônica de varredura. A partir destas técnicas, chegou-se à conclusão que o componente polar (EVASH se situa próximo à superfície da fibra. A utilização destas fibras em compósitos com resina epoxídica resultou em aumento considerável da resistência ao impacto e da temperatura de transição vítrea do material, indicando boa adesão interfacial matriz-fibra. Estas interações foram comprovadas por análise dinâmico-mecânicas.

Density Functional Calculation of the 0.5ML-Terminated Allyl Mercaptan/Si(100)-(2 × 1) Surface

International Nuclear Information System (INIS)

Chun-Mei, Tang; Kai-Ming, Deng; Xuan, Chen; Chuan-Yun, Xiao; Yu-Zhen, Liu; Qun-Xiang, Li

2009-01-01

The structural and electronic properties of the 0.5 ML-terminated allyl mercaptan (ALM)/Si(100)-(2 × 1) surface are studied using the density functional method. The calculated absorption energy of the ALM molecule on the 0.5 ML-terminated ALM/Si(100)-(2 × 1) surface is 3.36 eV, implying that adsorption is strongly favorable. The electronic structure calculations show that the ALM/Si(100)-(2 × 1), the clean Si(100)-(2 × 1), and the fully-terminated H/Si(100)-(2 × 1) surfaces have the nature of an indirect band gap semiconductor. The highest occupied molecular orbital is dominated by the ALM, confirming the mechanism proposed by Hossain for its chain reaction. (condensed matter: structure, mechanical and thermal properties)

Discrimination of the oral microbiota associated with high hydrogen sulfide and methyl mercaptan production.

Science.gov (United States)

Takeshita, Toru; Suzuki, Nao; Nakano, Yoshio; Yasui, Masaki; Yoneda, Masahiro; Shimazaki, Yoshihiro; Hirofuji, Takao; Yamashita, Yoshihisa

2012-01-01

Both hydrogen sulfide (H2S) and methyl mercaptan (CH(3)SH) are frequently detected in large amounts in malodorous mouth air. We investigated the bacterial composition of saliva of 30 subjects with severe oral malodor exhibiting extreme CH(3)SH/H(2)S ratios (high H(2)S but low CH(3)SH concentrations, n 5 14; high CH(3)SH but low H2S concentrations, n 5 16) and 13 subjects without malodor, using barcoded pyrosequencing analysis of the 16S rRNA gene. Phylogenetic community analysis with the UniFrac distance metric revealed a distinct bacterial community structure in each malodor group. The H2S group showed higher proportions of the genera Neisseria, Fusobacterium, Porphyromonas and SR1 than the other two groups, whereas the CH(3)SH group had higher proportions of the genera Prevotella, Veillonella,Atopobium, Megasphaera, and Selenomonas. Our results suggested that distinct bacterial populations in the oral microbiota are involved in production of high levels of H2S and CH3SH in the oral cavity.

New Look at odorization levels for propane gas. [Ethyl mercaptan; thiophane; equilibrium K values

Energy Technology Data Exchange (ETDEWEB)

Whisman, M.L.; Goetzinger, J.W.; Cotton, F.O.; Brinkman, D.W.; Thompson, C.J.

1977-09-01

Nearly 4,000 persons participated in a study to evaluate three odorant systems in four test modes and at 24 different test sites. Participants included trained panels, untrained ERDA employees, and several thousand untrained volunteer evaluators. The classical testing technique and three modified test modes were used to represent a spectrum of conditions that would define the effect of environmental familiarity and mental distractions upon olfactory responses to LP-gas. Significant efforts were directed toward determination of odorant levels that not only can be detected but also will be detected. The study showed that in addition to defects of the nasal anatomy, psychological factors also affect olfactory responses, and that unfamiliarity with a given environment as well as anxieties or mental distractions can produce reduced awareness to odorants intended to warn individuals of the presence of LP-gas. A second part of the study involved a laboratory determination of equilibrium K-values for both ethyl mercaptan and thiophane at three temperatures. Novel sample handling and gas chromatographic techniques provided reproducible results which were in close agreement with theoretical predictions. (28 tables, 29 tables)

Steel corrosion in tributyl phosphate in the presence of water and ethyl mercaptan

International Nuclear Information System (INIS)

Pischik, L.M.; Tsinman, A.I.

1979-01-01

Studied is the corrosion of steels St3, 15Kh5M, 08Kh13, 10Kh14G14N4T, 08Kh18G8N2T, 10Kh17N13M2T in TBP, in mixtures of TBP with ethyl mercaptan (EM) and two-phase systems TBP-water and TBP-water-EM at 50-150 deg. In pure TBP St3 corrosion rate is low even at 150 deg. In the presence of water St 3 strongly corrodes at above 50 deg temperature in organic and water layers and also in gas phase. The steel-08Kh18G8N2T at 90 deg in acid TBP is passive and its corrosion rate is lower than 0.01 mm/year. In identical conditions the resistance of stainless steels increases together with chromium content but in TBP with acid number 100 and above at 150 deg all tested steels including steel-10Kh17N13M2T are slightly resistant. Thus, even in absence of corrosion active additions of EM the mixture of TBP-water at higher temperature is agressive in relation not only to carbon steel but also to stainless steels

Protection of Grain Products from Sitophilus oryzae (L.) Contamination by Anti-Insect Pest Repellent Sachet Containing Allyl Mercaptan Microcapsule.

Science.gov (United States)

Chang, Yoonjee; Lee, Soo-Hyun; Na, Ja Hyun; Chang, Pahn-Shick; Han, Jaejoon

2017-11-01

The purpose of this study was to develop an anti-insect pest repellent sachet to prevent Sitophilus oryzae (L.) (Coleoptera: Curculionidae) contamination in grain packaging. The anti-insect pest activities of essential oils (EOs) from garlic (Allium Sativum), ginger (Zingiber Officinalis), black pepper (Piper nigrum), onion (Allium cepa), and fennel (Foeniculum vulgare) as well as major compounds (allyl disulfide, AD; allyl mercaptan, AM) isolated from of garlic and onion (AD and AM) were measured against S. oryzae. The results revealed that garlic EO, onion EO, AD, and AM showed strong fumigant insecticidal activities. Among these, AM showed the highest acetylcholinesterase (AChE) inhibition rate, indicating that the fumigation insecticidal efficacy of AM is related with its AChE inhibition ability. Subsequently, the microcapsules were produced with a high efficiency (80.02%) by using AM as a core material and rice flour as a wall material. Finally, sachet composed of rice flour microcapsule containing 2% AM (RAM) was produced. Repellent assay was performed to measure anti-insect pest ability of the RAM sachet, showed remarkable repelling effect within 48 h both in the presence or absence of attractant. In a release profile of RAM sachet, it was expected to last over 20 mo during the distribution period of brown rice. Moreover, RAM sachet showed no undesirable changes to the sensory properties of the rice both before and after cooking. Taken together, these results suggest that the newly developed RAM sachet could be used as a packaging material to protect grain products from S. oryzae contamination. The rice weevil, Sitophilus oryzae (L.) (Coleoptera: Curculionidae), causes damages to stored products and its contamination in grain products has become a major problem in cereal market. To preserve brown rice, an anti-insect pest repellent sachet containing 2% allyl mercaptan was newly developed and it showed remarkable repellent abilities against S. oryzae. It

Self-healing of low-velocity impact damage in glass fabric/epoxy composites using an epoxy–mercaptan healing agent

International Nuclear Information System (INIS)

Yuan, Yan Chao; Qin, Shi Xiang; Ye, Yueping; Chen, Haibin; Wu, Jingshen; Rong, Min Zhi; Zhang, Ming Qiu; Yang, Gui Cheng

2011-01-01

Self-healing woven glass fabric-reinforced epoxy composite laminates were made by embedding epoxy- and mercaptan-loaded microcapsules. After being subjected to low-velocity impact, the laminates were able to heal the damage in an autonomic way at room temperature. The healing-induced reduction in the damaged areas was visualized using a scanning acoustic microscope. The rate of damage area reduction, which is closely related to the effect of crack rehabilitation and mechanical recovery, is a function of impact energy, content and size of the healing microcapsules. Minor damage, such as microcracks in the matrix, can be completely repaired by the healing system without manual intervention, including external pressure. Microcapsules with larger size and/or higher concentration are propitious for delivering more healing agent to cracked portions, while imposition of lateral pressure on damaged specimens forces the separated faces to approach each other. Both can improve the rate of damage area reduction in the case of severe damage

Enzymatic studies on the metabolism of the tetrahydrofurfuryl mercaptan moiety of thiamine tetrahydrofurfuryl disulfide, 2

International Nuclear Information System (INIS)

Fujita, Takeshi; Suzuoki, Ziro; Kozuka, Seizi; Oae, Shigeru.

1973-01-01

The second step in the enzymatic process responsible for the novel metabolic pathway of foreign mercaptans leading to methylsulfonyl metabolites was shown to be sulfoxidation, subsequent to S-methylation. By using [ 35 S] methyl tetrahydrofurfuryl sulfide (MTFS) and [ 35 S] methyl tetrahydrofurfuryl sulfoxide (MTFSO) as substrates, the occurrence and involvement of both sulfide and sulfoxide oxygenases were demonstrated in rat liver microsomes. Both activities required reduced nicotinamide adenine dinucleotide phosphate (NADPH) and O 2 . The reaction products were isolated and identified as MTFSO and its sulfone, respectively. The apparent Michaelis constants were 6.7x10 -4 M for MTFS and 9.1x10 -15 M for NADPH with sulfide oxygenase and 5.6x10 -3 M for MTFSO and 5.0x10 -5 M for NADPH with sulfoxide oxygenase, respectively. P-chloromercuribenzoate, P-chloromercuribenzenesulfonate, HgCl 2 , and menadione strongly inhibited both oxygenases. Polyanions, such as inorganic phosphate, pyrophosphate, sulfate, and ATP stimulated both enzyme activities, especially that of sulfoxide oxygenase. One atom of 18 O 2 was incorporated into the products in both enzyme reactions. No appreciable incorporation was observed from H 2 18 O. These results indicate that both enzyme systems are typical monooxygenases. (auth.)

Sensors based on Ag-loaded hematite (α-Fe2O3 nanoparticles for methyl mercaptan detection at room temperature

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Daniel Garcia

2017-06-01

Full Text Available Sensors based on Ag/α-Fe2O3 nanoparticles have been prepared by the coprecipitation method for sensing methyl mercaptan at room temperature. X-ray diffraction patterns of samples matched perfectly with characteristic peaks of hematite with no peaks assigned to Ag even at the highest concentration. STEM images and EDX analysis revealed the presence of Ag nanoparticles (from 2 to 5 nm which were highly dispersed onto α-Fe2O3 surface with an Ag/Fe ratio from 0.014 to 0.099. The Ag nanoparticles were deposited on the hematite surface. Sensing tests of Ag-loaded hematite nanoparticles showed much higher response signal than the unmodified sensor. Hematite loaded with 3%(Wt Ag showed the highest response with a linear dependence from 20 to 80 ppm. The sensor also depicted a good selectivity and stability during 4 days with short recovery time. The high dispersion of reduced Ag evaluated by XPS analysis played an important chemical role in the sensing mechanism that favored the contact of CH3SH with oxygen.

Porphyromonas gingivalis hydrogen sulfide enhances methyl mercaptan-induced pathogenicity in mouse abscess formation.

Science.gov (United States)

Nakamura, Suguru; Shioya, Koki; Hiraoka, B Yukihiro; Suzuki, Nao; Hoshino, Tomonori; Fujiwara, Taku; Yoshinari, Nobuo; Ansai, Toshihiro; Yoshida, Akihiro

2018-04-01

Porphyromonas gingivalis produces hydrogen sulfide (H2S) from l-cysteine. However, the role of H2S produced by P. gingivalis in periodontal inflammation is unclear. In this study, we identified the enzyme that catalyses H2S production from l-cysteine and analysed the role of H2S using a mouse abscess model. The enzyme identified was identical to methionine γ-lyase (PG0343), which produces methyl mercaptan (CH3SH) from l-methionine. Therefore, we analysed H2S and CH3SH production by P. gingivalis W83 and a PG0343-deletion mutant (ΔPG0343) with/without l-cysteine and/or l-methionine. The results indicated that CH3SH is produced constitutively irrespective of the presence of l-methionine, while H2S was greatly increased by both P. gingivalis W83 and ΔPG0343 in the presence of l-cysteine. In contrast, CH3SH production by ΔPG0343 was absent irrespective of the presence of l-methionine, and H2S production was eliminated in the absence of l-cysteine. Thus, CH3SH and H2S production involves different substrates, l-methionine or l-cysteine, respectively. Based on these characteristics, we analysed the roles of CH3SH and H2S in abscess formation in mice by P. gingivalis W83 and ΔPG0343. Abscess formation by P. gingivalis W83, but not ΔPG0343, differed significantly in the presence and absence of l-cysteine. In addition, the presence of l-methionine did not affect the size of abscesses generated by P. gingivalis W83 and ΔPG0343. Therefore, we conclude that H2S produced by P. gingivalis does not induce inflammation; however, H2S enhances inflammation caused by CH3SH. Thus, these results suggest the H2S produced by P. gingivalis plays a supportive role in inflammation caused by methionine γ-lyase.

Mercury separation from concentrated potassium iodide/iodine leachate using Self-Assembled Mesoporous Mercaptan Support (SAMMS) technology

International Nuclear Information System (INIS)

Mattigod, S.V.; Feng, X.; Fryxell, G.E.

1997-10-01

A study was conducted to demonstrate the effectiveness of a novel adsorber, the Self-Assembled Mesoporous Mercaptan Support (SAMMS) material to remove mercury (Hg) from potassium iodide/iodine (KI/I 2 ) waste streams. This study included investigations of the SAMMS material''s binding kinetics, loading capacity, and selectivity for Hg adsorption from surrogate and actual KI/I 2 waste solutions. The kinetics data showed that binding of Hg by the adsorber material occurs very rapidly, with 82% to 95% adsorption occurring within the first 5 min. No significant differences in the rate of adsorption were noted between pH values of 5 and 9 and at Hg concentrations of ∼100 mg/1. Within the same range of pH values, an approximate four-fold increase in initial Hg concentration resulted in a two-fold increase in the rate of adsorption. In all cases studied, equilibrium adsorption occured within 4 h. The loading capacity experiments in KI/I 2 surrogate solutions indicated Hg adsorption densities between 26 to 270 mg/g. The loading density increased with increasing solid: solution ratio and decreasing iodide concentrations. Values of distribution coefficients (1.3x10 5 to >2.6x10 8 ml/g) indicated that material adsorbs Hg with very high specificity from KI/I 2 surrogate solutions. Reduction studies showed that compared to metallic iron (Fe), sodium dithionite can very rapidly reduce iodine as the triiodide species into the iodide form. Adsorption studies conducted with actual KI/I 2 leachates confirmed the highly specific Hg adsorption properties (K d >6x10 7 to>1x10 8 ml//g) of the adsorber material. Following treatment, the Hg concentrations in actual leachates were below instrumental detection limits (i.e., < 0.00005 mg/l), indicating that the KI solutions can be recycled

Micro-oxygenation does not eliminate hydrogen sulfide and mercaptans from wine; it simply shifts redox and complex-related equilibria to reversible oxidized species and complexed forms.

Science.gov (United States)

Vela, Eduardo; Hernandez-Orte, Purificación; Franco-Luesma, Ernesto; Ferreira, Vicente

2018-03-15

This work seeks to assess the effects of micro-oxygenation (MOX) on the present and potential levels of Volatile Sulfur Compounds (VSCs) of wine. With such purpose, three red wines with a tendency to develop sulfury off-odors were subjected to three different MOX conditions (4.4-20mg/L delivered at 0.05 or 0.2mg/L/day). Samples were further subjected to Accelerated Reductive aging (AR) and analyzed for free and Brine Releasable (BR) VSCs and redox potential. Although MOX induced strong decreases in the levels of all free VSCs, hardly affected the ability of the wine to release back hydrogen sulfide and other mercaptans during AR-aging. During aging BR-levels of MOX samples became in most cases similar or higher than non-oxygenated controls. BR-levels and the fractions free/BR follow characteristic sigmoid plots when represented versus redox potential suggesting that all changes are the result of reversible equilibria between free, metal-complexed and oxidized forms of VSCs. Copyright © 2017 Elsevier Ltd. All rights reserved.

Cometabolic degradation of ethyl mercaptan by phenol-utilizing Ralstonia eutropha in suspended growth and gas-recycling trickle-bed reactor.

Science.gov (United States)

Sedighi, Mahsa; Zamir, Seyed Morteza; Vahabzadeh, Farzaneh

2016-01-01

The degradability of ethyl mercaptan (EM), by phenol-utilizing cells of Ralstonia eutropha, in both suspended and immobilized culture systems, was investigated in the present study. Free-cells experiments conducted at EM concentrations ranging from 1.25 to 14.42 mg/l, showed almost complete removal of EM at concentrations below 10.08 mg/l, which is much higher than the maximum biodegradable EM concentration obtained in experiments that did not utilize phenol as the primary substrate, i.e. 2.5 mg/l. The first-order kinetic rate constant (kSKS) for EM biodegradation by the phenol-utilizing cells (1.7 l/g biomass/h) was about 10 times higher than by cells without phenol utilization. Immobilized-cells experiments performed in a gas recycling trickle-bed reactor packed with kissiris particles at EM concentrations ranging from 1.6 to 36.9 mg/l, showed complete removal at all tested concentrations in a much shorter time, compared with free cells. The first-order kinetic rate constant (rmaxKs) for EM utilization was 0.04 l/h for the immobilized system compared to 0.06 for the suspended-growth culture, due to external mass transfer diffusion. Diffusion limitation was decreased by increasing the recycling-liquid flow rate from 25 to 65 ml/min. The removed EM was almost completely mineralized according to TOC and sulfate measurements. Shut down and starvation experiments revealed that the reactor could effectively handle the starving conditions and was reliable for full-scale application. Copyright © 2015 Elsevier Ltd. All rights reserved.

Appropriate sample bags and syringes for preserving breath samples in breath odor research : a technical note

NARCIS (Netherlands)

Winkel, E. G.; Tangerman, A.

It is now generally accepted that the volatile sulfur compounds (VSCs) hydrogen sulfide, methyl mercaptan and dimethyl sulfide are the main contributors to halitosis when of oropharyngeal origin. The VSCs hydrogen sulfide and methyl mercaptan are the major causes of bad breath in oral malodour

Gamma radiolysis of aliphatic sulfur compounds in aqueous solutions. A study to contribute to the analysis of the end products of the OH radical-induced oxidation of aliphatic mercaptanes, sulfides, and disulfides

International Nuclear Information System (INIS)

Weiss, J.

1982-01-01

By identifying and determining numerous hitherto unknown end products, the study in hand contributes to a better insight into the radiation chemical processes occurring in OH radical-induced oxidation of aliphatic sulfur compounds. An extraction method has been developed for the qualitative and quantitative analysis of end products in aqueous solution in order to determine these compounds down to the level of trace amounts. Separation of endproducts is achieved by means of gas chromatography and high-pressure liquid chromatography, subsequent identification by GC-MS analysis. Aliphatic mercaptanes are oxidized by OH radicals to thiyl radicals which after combination can be detected as disulfide. At high radiation doses, secondary reactions will lead to polysulfides of which the homologues could first be prepared as the pure substance. The end products of the γ-radiolysis of aliphatic thioethers are determined to be dithia compounds, symmetrical or asymmetrical disulfides, or polysulfides, depending on the thioethers. With some end products, the radiation chemical yield is found to be a function of the absorbed dose so that material balances are impossible. Intermediate thiyl, α-alkyl mercaptoalkyl or alkyl radicals can be captured by tetramethyl ethylene, cyclohexene or p-benzoquinone, and can then be identified as the relevant adducts. (orig./RB) [de

Hydrogen-transfer and charge-transfer in photochemical and radiation induced reactions. Progress report, November 1, 1975--October 31, 1976

International Nuclear Information System (INIS)

Cohen, S.G.

1976-10-01

The relative importance of light absorption, quenching of triplet, and hydrogen transfer repair has been examined in retardation by mercaptans of photoreduction of aromatic ketones by alcohols. In the reduction of benzophenone by 2-propanol, retardation is efficient and, after correction for the first two effects, is due entirely to hydrogen-transfer repair, as indicated by deuterium labeling. In reduction of acetophenone by α-methylbenzyl alcohol, repair by hydrogen transfer is also operative. In reduction of benzophenone by benzhydrol, retardation is less efficient and is due to quenching, as the ketyl radical does not abstract hydrogen from mercaptan rapidly in competition with coupling. Deuterium isotope effects are discussed in terms of competitive reactions. Photoreduction of benzophenone by 2-butylamine and by triethylamine is retarded by aromatic mercaptans and disulfides. Of the retardation not due to light absorption and triplet quenching by the sulfur compounds, half is due to hydrogen-transfer repair, as indicated by racemization and deuterium labeling. The remainder is attributed to quenching by the sulfur compound of the charge-transfer-complex intermediate. Photoreduction by primary and secondary amines, but not by tertiary amines, is accelerated by aliphatic mercaptans. The acceleration is attributed to catalysis of hydrogen transfer by the mercaptan in the charge-transfer complex. The effect is large in hydrocarbon solvent, less in polar organic solvents and absent in water

Comportamento de cura de adesivo epoxídico contendo grupo mercaptana avaliado por espectroscopia no infravermelho (MIR/NIR e calorimetria exploratória diferencial (DSC Cure behavior of epoxy adhesive containig mercaptan group evaluated by infrared spectroscopy (MIR/NIR and differential scanning calorimetry (DSC

Directory of Open Access Journals (Sweden)

Hilzette P. C. Andrade

2008-01-01

Full Text Available No presente trabalho, a flexibilidade de um adesivo epoxídico contendo diglicidiléter de bisfenol A (DGEBA e dietilenotriamina (DETA como agente de cura foi modificada pela adição de um segundo componente contendo grupos mercaptana (CAPCURE. A adição de amianto ao adesivo contendo CAPCURE também foi avaliada. As reações entre os grupos epoxídicos e os grupos amina, assim como entre os grupos epoxídicos e os grupos mercaptana, foram estudadas nas regiões espectrais do infravermelho médio (MIR e próximo (NIR. Observou-se que o amianto não interfere nas reações de cura e que a espectroscopia FT-NIR evidencia melhor as alterações espectrométricas ocorridas durante as reações em relação à análise FT-MIR. O tempo das reações de cura foi monitorado por calorimetria exploratória diferencial (DSC, observando-se que a introdução do CAPCURE acelerou a cura da resina. A energia de ativação (Ea das reações de cura foi obtida pelos métodos de Barrett e Borchardt-Daniels. Os adesivos contendo CAPCURE mostraram Ea em torno de 30 kJ.mol-1, enquanto o adesivo DGEBA/DETA apresentou Ea de 46 kJ.mol-1, ambas calculadas pelo método de Barrett.In the present work, the flexibility of an epoxy adhesive containing diglycidylether of bisphenol-A (DGEBA and diethylenetriamine (DETA as curing agent was changed by the addition of a second component containing mercaptan groups (CAPCURE. The addition of asbestos as a filler in the adhesive containing CAPCURE was also evaluated. Epoxy-amine and epoxy-mercaptan reactions were studied in NIR and MIR spectral regions. The filler addition did not cause influence on the cure reactions and spectrometric changes of cure reactions could be better observed by FT-NIR than FT-MIR analysis. The cure reaction time was monitored by DSC experiments and it was observed that the introduction of CAPCURE accelerated the cure reaction. The activation energies (Ea of curing reactions were obtained using Barrett

The Impact of Hazardous Chemicals on Macrophages

Science.gov (United States)

2012-04-01

8217MetBis) * Parathion solution (Parat) * Perchloromethyl mercaptan CChSCl (PClMM) * Propyl chloroformate ClCOzCHzCHzCH3 (PropClF) * *Abbreviation...0.53 (J.!M) 3.4nM 13 Perchloromethyl mercaptan 9.05 1.81 9.05 14 Propyl chloroformate 8.7 5.53 87 22 DTRA Basic Research Grant HDTRAI-07- 1-0027...production of semiconductor devices like integrated circuits and also used in laser and light-emitting diodes (LEOs). Butyl chloroformate (ButCIF

Adsorption/oxidation of sulfur-containing gases on nitrogen-doped activated carbon

Directory of Open Access Journals (Sweden)

Liu Qiang

2016-01-01

Full Text Available Coconut shell-based activated carbon (CAC was used for the removal of methyl mercaptan (MM. CAC was modified by urea impregnation and calcined at 450°C and 950°C. The desulfurization activity was determined in a fixed bed reactor under room temperature. The results showed that the methyl mercaptan adsorption/oxidation capacity of modified carbon caicined at 950°C is more than 3 times the capacity of original samples. On the other hand, the modified carbon caicined at 950°C also has a high capacity for the simultaneous adsorption/oxidation of methyl mercaptan and hydrogen sulfide.The introduce of basic nitrogen groups siginificantly increases the desulfurization since it can facilitate the electron transfer process between sulfur and oxygen. The structure and chemical properties are characterized using Boehm titration, N2 adsorption-desorption method, thermal analysis and elemental analysis. The results showed that the major oxidation products were dimethyl disulfide and methanesulfonic acid which adsorbed in the activated carbon.

The combined removal of methyl mercaptan and hydrogen sulfide via an electro-reactor process using a low concentration of continuously regenerable Ag(II) active catalyst

International Nuclear Information System (INIS)

Muthuraman, Govindan; Chung, Sang Joon; Moon, Il Shik

2011-01-01

Highlights: → Simultaneous removal of H 2 S and CH 3 SH was achieved at electro-reactor. → Active catalyst Ag(II) perpetually regenerated in HNO 3 medium by electrochemical cell. → CH 3 SH destruction follows two reaction pathways. → H 2 S induced destruction of CH 3 SH has identified. → Low concentration of active Ag(II) (12.5 x 10 -4 mol L -1 ) is enough for complete destruction. - Abstract: In this study, an electrocatalytic wet scrubbing process was developed for the simultaneous removal of synthetic odorous gases namely, methyl mercaptan (CH 3 SH) and hydrogen sulfide (H 2 S). The initial process consists of the absorption of CH 3 SH and H 2 S gases by an absorbing solution, followed by their mediated electrochemical oxidation using a low concentration of active Ag(II) in 6 M HNO 3 . Experiments were conducted under different reaction conditions, such as CH 3 SH and H 2 S loadings, active Ag(II) concentrations and molar flow rates. The cyclic voltammetry for the oxidation of CH 3 SH corroborated the electro-reactor results, in that the silver in the 6 M HNO 3 reaction solution significantly influences the oxidation of CH 3 SH. At a low active Ag(II) concentration of 0.0012 M, the CH 3 SH removal experiments demonstrated that the CH 3 SH degradation was steady, with 100% removal at a CH 3 SH loading of 5 g m -3 h -1 . The electro-reactor and cyclic voltammetry results indicated that the removal of H 2 S (100%) follows a mediated electrocatalytic oxidation reaction. The simultaneous removal of 100% of the CH 3 SH and H 2 S was achieved, even with a very low active Ag(II) concentration (0.0012 M), as a result of the high efficiency of the Ag(II). The parallel cyclic voltammetry results demonstrated that a process of simultaneous destruction of both CH 3 SH and H 2 S follows an H 2 S influenced mediated electrocatalytic oxidation. The use of a very low concentration of the Ag(II) mediator during the electro-reactor process is promising for the complete

Kinetics of aerobic oxidation of volatile sulfur compounds in wastewater and biofilm from sewers

DEFF Research Database (Denmark)

Rudelle, Elise Alice; Vollertsen, Jes; Hvitved-Jacobsen, Thorkild

2013-01-01

Laboratory experiments were conducted to investigate the kinetics of aerobic chemical and biological oxidation of selected odorous volatile sulfur compounds (VSCs) by wastewater and biofilm from sewers. The VSCs included methyl mercaptan (MeSH), ethyl mercaptan (EtSH), dimethyl sulfide (DMS......-spot downstream of a force main and the other was a gravity sewer transporting young aerobic wastewater. The kinetics of VSC oxidation for both wastewater and suspended biofilm samples followed a first-order rate equation. The average values of the reaction rate constants demonstrated the following order...... in the aerobic wastewater....

In-situ quartz crystal microgravimetric studies of molecular adsorbates containing thiol and hydroquinone moieties bound to Au(111) surfaces in aqueous electrolytes

Energy Technology Data Exchange (ETDEWEB)

Mo, Y.; Sukenik, C.; Sandifer, M. [Case Western Univ., Cleveland, OH (United States); Barriga, R.J.; Soriaga, M.P.; Scherson, D. [Texas A& M Univ., College Station, TX (United States)

1995-12-01

The microgravimetric properties of monolayers of 2, 5-dihydroxythiophenol, 2,5-dihydroxybenzyl mercaptan, and 2, 5-dihydroxy-4-methylbenzyl mercaptan adsorbed on Au(111) single crystal electrodes were examined by in situ quartz crystal microbalance techniques in aqueous perchloric acid electrolytes. The results obtained are consistent with the reversible loss of an average of about three waters per adsorbed molecule as the layers are oxidized and subsequently reduced. These observations provide evidence for discrete changes in the extent of bound water within the hydroquinone/quinone layer as the oxidation state of the monolayer is changed. 9 refs., 4 figs.

A molecular imprinted SPR biosensor for sensitive determination of citrinin in red yeast rice.

Science.gov (United States)

Atar, Necip; Eren, Tanju; Yola, Mehmet Lütfi

2015-10-01

A novel and sensitive molecular imprinted surface plasmon resonance (SPR) biosensor was developed for selective determination of citrinin (CIT) in red yeast rice. Firstly, the gold surface of SPR chip was modified with allyl mercaptane. Then, CIT-imprinted poly(2-hydroxyethyl methacrylate-methacryloylamidoglutamic acid) (p(HEMA-MAGA)) film was generated on the gold surface modified with allyl mercaptane. The unmodified and imprinted surfaces were characterized by Fourier transform infrared (FTIR) spectroscopy, atomic force microscopy (AFM) and contact angle measurements. The linearity range and the detection limit were obtained as 0.005-1.0 ng/mL and 0.0017 ng/mL, respectively. The SPR biosensor was applied to determination of CIT in red yeast rice sample. Copyright © 2015 Elsevier Ltd. All rights reserved.

Uptake and utilization of sulfonic acids in the cyanobacterial strains Anabaena variabilis and Plectonema 73110

International Nuclear Information System (INIS)

Biedlingmaier, S.; Schmidt, A.

1987-01-01

Growth of several cyanobacteria was examined on ethane sulfonate and taurine as only sulfur source. Comparing two strains with differential utilization of sulfonic acids (Anabaena variabilis and Synechococcus 6301) demonstrated that actual growth was coupled to the presence of an active sulfonate transport system due to species specific properties and nutritional conditions. Sulfonate uptake in Anabaena variabilis was characterized by a pH optimum of 6.5, a structural specificity for sulfonates, missing Na + dependence, and phosphate stimulation. Radiolabeled ethane sulfonate and taurine was metabolized to products of normal sulfur metabolism. Also considerable amounts of 35 S-labeled volatiles (mercaptanes and sulfide) could be detected, suggesting a degradation mechanism via reduction to mercaptanes and cleavage of the C-S bond. (orig.)

Uses of Tc99m complexes

International Nuclear Information System (INIS)

Kubiatowicz, D.O.; Bolles, T.F.

1978-01-01

The invention deals with the use of a complex of the radioactive metastable isotope Tcsup(99m) together with water-soluble mercaptane for the preparation of a parenterally administered renal diagnostic agent. (VJ/orig.) [de

Handbook for Evaluating Ecological Effects of Pollution at DARCOM installations. Volume 2, Essential Background Data. (Installation Environmental Impact Assessment)

Science.gov (United States)

1979-12-01

Nitrates Sulfur dioxide Xylene Nitrites Oxides of nitrogen Mercaptans "Red Water" Carbon monoxide Chlorine Acids: Ketones Fluorine Hydrochloric Esters...Trichloroethylene Varnishes Methylchloroform Undercoatings Mineral spirits Liquid styrene Naphtha Adhesives Halgenated hydrocarbons Nonmethane hydrocarbons

Factors Influencing Degradation of Mercaptans by Thiobacillus ...

African Journals Online (AJOL)

Degradation of methylmercaptans by Thiobacillus thioparus TK-m was influenced by pH of the reaction medium. Ratios of headspace concentrations in empty vials and those of acidified buffer solutions were less than 1.0. 95% of the H2S was in headspace with the remaining 5% in solution upon acidification. The values for ...

Galloylated proanthocyanidins from shea (Vitellaria paradoxa) meal have potent anthelmintic activity against Ascaris suum

DEFF Research Database (Denmark)

Ramsay, A; Williams, A R; Thamsborg, S M

2016-01-01

Proanthocyanidins (PA) from shea (Vitellaria paradoxa) meal were investigated by thiolytic degradation with benzyl mercaptan and the reaction products were analysed by high performance liquid chromatography-mass spectrometry. These PA were galloylated (≈40%), contained only B-type linkages and ha...

Dietary composition affects odour emissions from meat chickens

Directory of Open Access Journals (Sweden)

Nishchal K. Sharma

2015-03-01

Full Text Available Abatement of odour emissions has become an important consideration to agricultural industries, including poultry production. The link between diet and odour emissions was studied in two experiments using Ross 308 male meat chickens reared in specially designed chambers in a climate controlled room. In the first experiment, two treatments were compared using three replicates of two birds per chamber. Two wheat-soy based treatment diets were formulated with or without canola seed, an ingredient rich in sulfur amino acids. Treatment 1 (T1 had 13.39 MJ/kg ME (as fed and used 60 g/kg canola seed without corn while Treatment 2 (T2 contained 12.90 MJ/kg ME (as fed and used 150 g/kg corn without canola seed. In the second experiment, birds were assigned to three dietary treatments of five replicates with five birds per replicate (chamber. The basal starter, grower and finisher diets in the control group (SBM group contained soybean meal in the range of 227–291 g/kg (as fed as the main protein source. The other treatments (CM and MBM groups contained either high levels of canola meal (174–190 g/kg or meat meal (74–110 g/kg at the expense of soybean meal. In both experiments, diets were isocaloric, isonitrogenous and contained similar digestible amino acid contents as per 2007 Aviagen Ross 308 guidelines. Emissions of odour were measured using Fourier transform infrared (FTIR spectroscopy. In both experiments, major odorous compounds detected included 2,3-butanedione (diacetyl, 2-butanone, dimethyl disulfide, methyl mercaptan, ethyl mercaptan, 2-butanol, 3-methyl-butanal, phenol and m-cresol. In the first experiment, T1 (with canola seed produced higher concentration of methyl mercaptan (P < 0.05 and lower diacetyl (P < 0.01 than T2. In the second experiment, methyl mercaptan emission was higher in SBM group (P = 0.01 and total elemental sulfur were higher in SBM and CM groups up to day 24 (P < 0.01. Results of these experiments

40 CFR Appendix A to Part 414 - Non-Complexed Metal-Bearing Waste Streams and Cyanide-Bearing Waste Streams

Science.gov (United States)

2010-07-01

... Mercaptan/Ethanol + Hydrogen sulfide Methanol/H.P. Synthesis from natural gas via synthetic gas Oxo Alcohols... + Ammonia n-Propyl alcohol/Hydrogenation of propionaldehyde, Oxo process SAN resin/Suspension polymerization... methanol Acetaldehyde/Oxidation of ethylene with cupric chloride catalyst Acetic acid/Catalytic oxidation...

Vapor–Liquid–Liquid Equilibrium Measurements and Modeling of Ethanethiol + Methane + Water, 1-Propanethiol + Methane + Water and 1-Butanethiol + Methane + Water Ternary Systems at 303, 335, and 365 K and Pressure Up to 9 MPa

DEFF Research Database (Denmark)

Awan, Javeed; Kontogeorgis, Georgios; Tsivintzelis, Ioannis

2013-01-01

New vapor–liquid–liquid equilibrium (VLLE) data for ethanethiol + methane + water, 1-propanethiol + methane + water, and 1-butanethiol + methane + water ternary systems have been measured at three temperatures (303, 335, and 365 K) and pressures up to 9 MPa. A “static-analytic” method was used...... for performing the measurements; the total system pressure was maintained by CH4. The objective of this work is to provide experimental VLLE data for mixtures of mercaptans (thiols) with other natural gas contents at its crude form, for which no data are available in the open literature. Such data will help...... the industrial modeling of processes relevant to reduction of sulfur emissions. The Cubic-Plus-Association (CPA) equation of state was applied to describe the phase behavior of the investigated systems. It is shown that the CPA EoS satisfactorily describes the solubilities of mercaptans (thiols) in all phases...

Seeded emulsion polymerization of butadiene. 1. The propagation rate coefficient

NARCIS (Netherlands)

Verdurmen, E.M.F.J.; Dohmen, E.H.M.; Verstegen, J.M.; Maxwell, I.A.; German, A.L.; Gilbert, R.G.

1993-01-01

The kinetics of the emulsifier-free, seeded polymn. of butadiene (I) at 60 Deg in Smith-Ewart interval III were studied in presence of Na peroxodisulfate initiator and tert-dodecyl mercaptan. The fractional conversion was based on gravimetrically calibrated online densitometry and was highly

Photodegradation of odorous 2-mercaptobenzoxazole through zinc oxide/hydroxyapatite nanocomposite

DEFF Research Database (Denmark)

Buazar, Foad; Alipouryan, S.; Kroushawi, Feisal

2015-01-01

In this study, ZnO/HAP nanocomposite with excellent photocatalytic activities was successfully synthesized by sol–gel method and used for degradation of 2-mercaptobenzoxazole (MBO) as model of odorous mercaptan compound in water. To optimize the performance of ZnO/HAP photocatalytic capabilities,...

Deodorization and dearomatization of kerosene by liquid extraction ...

African Journals Online (AJOL)

Sulphur compounds determination was by the Nickel Reduction Method. The specific gravity, aromatic content, smoke point, flash point, mercaptan sulphur, initial and end boiling points and the k-factor of the kerosene were determined using standard procedures. Also the distribution of sulphur compounds in distillation ...

Environmental Assessment for Enhanced Use Lease of U.S. Air Force Lands to the City of North Las Vegas for Construction and Operation of a Water Reclamation Facility, Nellis Air Force Base, Nevada

Science.gov (United States)

2008-01-01

associated thermal spring systems within the Warm Springs in Nevada. No - Project area located west of the Muddy River. Lahontan cutthroat trout ...include a section to address how the source intends to mitigate for odor (i.e. mercaptans, indoles, skatoles, and amines) or destruction of digester

Polymercaptanized soybean oil – properties and tribological characterization

Science.gov (United States)

Polymercaptanized vegetable oils are produced in industrial scale by the addition of hydrogen sulfide across double bonds or epoxides of vegetable oils, in the presence of UV-light. To date, soybean oil, epoxidized soybean oil, and castor oil has been mercaptanized using such a procedure. Depending ...

Adsorption of volatile sulphur compounds onto modified activated carbons: Effect of oxygen functional groups

International Nuclear Information System (INIS)

Vega, Esther; Lemus, Jesús; Anfruns, Alba; Gonzalez-Olmos, Rafael; Palomar, José; Martin, María J.

2013-01-01

Highlights: • HNO 3 oxidation incorporates a higher amount of functionalities than O 3 oxidation. • The loss of porosity is compensated by the massive incorporation of oxygen groups. • HNO 3 oxidation increases OH groups in AC and the ETM and DMS adsorption capacities. • The oxygen functional groups in the AC surface did not affect the DMDS adsorption. • COSMO-RS predicts the important role of OH groups for VSC adsorption. -- Abstract: The effect of physical and chemical properties of activated carbon (AC) on the adsorption of ethyl mercaptan, dimethyl sulphide and dimethyl disulphide was investigated by treating a commercial AC with nitric acid and ozone. The chemical properties of ACs were characterised by temperature programme desorption and X-ray photoelectron spectroscopy. AC treated with nitric acid presented a larger amount of oxygen functional groups than materials oxidised with ozone. This enrichment allowed a significant improvement on adsorption capacities for ethyl mercaptan and dimethyl sulphide but not for dimethyl disulphide. In order to gain a deeper knowledge on the effect of the surface chemistry of AC on the adsorption of volatile sulphur compounds, the quantum-chemical COSMO-RS method was used to simulate the interactions between AC surface groups and the studied volatile sulphur compounds. In agreement with experimental data, this model predicted a greater affinity of dimethyl disulphide towards AC, unaffected by the incorporation of oxygen functional groups in the surface. Moreover, the model pointed out to an increase of the adsorption capacity of AC by the incorporation of hydroxyl functional groups in the case of ethyl mercaptan and dimethyl sulphide due to the hydrogen bond interactions

Adsorption of volatile sulphur compounds onto modified activated carbons: Effect of oxygen functional groups

Energy Technology Data Exchange (ETDEWEB)

Vega, Esther, E-mail: esther@lequia.udg.cat [LEQUIA, Institute of the Environment, University of Girona, Campus Montilivi, Girona, Catalonia E-17071 (Spain); Lemus, Jesús [Universidad de Madrid, Sección de Ingeniería Química, Cantoblanco, Madrid E-28049 (Spain); Anfruns, Alba; Gonzalez-Olmos, Rafael [LEQUIA, Institute of the Environment, University of Girona, Campus Montilivi, Girona, Catalonia E-17071 (Spain); Palomar, José [Universidad de Madrid, Sección de Ingeniería Química, Cantoblanco, Madrid E-28049 (Spain); Martin, María J. [LEQUIA, Institute of the Environment, University of Girona, Campus Montilivi, Girona, Catalonia E-17071 (Spain)

2013-08-15

Highlights: • HNO{sub 3} oxidation incorporates a higher amount of functionalities than O{sub 3} oxidation. • The loss of porosity is compensated by the massive incorporation of oxygen groups. • HNO{sub 3} oxidation increases OH groups in AC and the ETM and DMS adsorption capacities. • The oxygen functional groups in the AC surface did not affect the DMDS adsorption. • COSMO-RS predicts the important role of OH groups for VSC adsorption. -- Abstract: The effect of physical and chemical properties of activated carbon (AC) on the adsorption of ethyl mercaptan, dimethyl sulphide and dimethyl disulphide was investigated by treating a commercial AC with nitric acid and ozone. The chemical properties of ACs were characterised by temperature programme desorption and X-ray photoelectron spectroscopy. AC treated with nitric acid presented a larger amount of oxygen functional groups than materials oxidised with ozone. This enrichment allowed a significant improvement on adsorption capacities for ethyl mercaptan and dimethyl sulphide but not for dimethyl disulphide. In order to gain a deeper knowledge on the effect of the surface chemistry of AC on the adsorption of volatile sulphur compounds, the quantum-chemical COSMO-RS method was used to simulate the interactions between AC surface groups and the studied volatile sulphur compounds. In agreement with experimental data, this model predicted a greater affinity of dimethyl disulphide towards AC, unaffected by the incorporation of oxygen functional groups in the surface. Moreover, the model pointed out to an increase of the adsorption capacity of AC by the incorporation of hydroxyl functional groups in the case of ethyl mercaptan and dimethyl sulphide due to the hydrogen bond interactions.

Plasmas pour la destruction de l'H2S et des mercaptans Plasmas for Destruction of H2s and Mercaptans

Directory of Open Access Journals (Sweden)

Czernichowski A.

2006-12-01

Full Text Available Cet article passe en revue l'utilisation des plasmas comme milieu activateurs d'une oxydation de H2S ou CH3SH dilués dans l'air, le CO2 ou la vapeur d'eau, à fins de conversion en SO, moins malodorant. Le produit peut être ensuite utilisé comme réactif dans un processus similaire à celui de Claus, en présence d'eau, ce qui permet de convertir deux fois plus de polluants initiaux en soufre élémentaire. Une attention particulière est portée aux décharges électriques glissantes (GlidArc. Ces décharges puissantes produisent un plasma non thermique qui active des réactions oxydatrices. La plupart des expériences ont été réalisées en utilisant les réacteurs GlidArc-I à un ou à quatre étages. Les sulfures dilués dans l'air dans des concentrations initiales atteignant jusqu'à 1 %( H2S ou 0,1 % (CH3SH ont été traités sous des flux jusqu'à 70 m3(n/h d'air pollué et sous une puissance de 5 kW. Les essais ont été réalisés sous 1 atm. Une dépollution jusqu'à 100 % a été obtenue moyennant un coût énergétique assez bas dépendant de la concentration initiale du polluant : environ 1000 kWh par kilogramme de soufre extrait pour 100 ppm de H2S et seulement 10 kWh/kg pour 1 % initial d'H2S dans l'air. Pratiquement les mêmes coûts ont été observés dans le cas de mélanges CH3SH-air. En utilisant une très simple douche en recirculation d'eau qui lave les gaz sortants (l'eau se sature avec le SO2 et capture ainsi l'H2S non traité nous avons divisé ces coûts d'énergie par trois, en évitant également l'émission de SO2, et en obtenant du soufre non toxique. Un nouveau principe (et réacteur GlidArc-II est ensuite présenté ; il s'agit d'une brosseà décharges électriques. Nos premiers tests sont très prometteurs car dès à présent, nous divisons déjà la dépense énergétique par deux par rapport au GlidArc-I. L'échelle industrielle peut par conséquent être envisagée. Plasmas are reviewed as activation media for an oxidation of H2S or CH3SH diluted in air, CO2 or steam in order to convert them into less malodorous SO2. The product can be then used as a reagent in a Claus-like process in presence of water to convert twice as much of initial pollutants into elemental sulfur. A particular attention is devoted to the gliding electrical discharges (GlidArc. These powerful discharges produce non-thermal plasma, which activates oxidation reactions. Most of experiments were performed using one and four-stage GlidArc-I reactors. Air-diluted sulfides at initial concentrations up to 1% (H2S or 0. 1% (CH3SH were processed at up to 70 m3(n/h flow rate and 5 kW power scale. The tests were done at 1 atm. Up to 100% clean-up was obtained at a quite low energy cost depending on initial pollutant concentration: roughly 1000 kWh per 1 kg of removed sulfur at 100 ppm of H2S, but only 10 kWh/kg for 1% initial H2S in air. Almost the same energies were needed in the case of CH3SH-air mixtures. Using a very simple washing column in which water saturates with the produced SO2 and so captures unprocessed H2S we cut these process energy by three, avoiding the SO2 emission and obtaining non-toxic sulfur. New development based on GlidArc-ll brush-like electric discharges is also presented. Preliminary tests are very promising as the energy expense is already cut down by a factor of two with respect to the GlidArc-I devices. Up to industrial scale tests can be therefore performed.

Photodissociation dynamics of ethanethiol in clusters: complementary information from velocity map imaging, mass spectrometry and calculations

Czech Academy of Sciences Publication Activity Database

Svrčková, Pavla; Pysanenko, Andriy; Lengyel, Jozef; Rubovič, Peter; Kočišek, Jaroslav; Poterya, Viktoriya; Slavíček, Petr; Fárník, Michal

2015-01-01

Roč. 17, č. 39 (2015), s. 25734-25741 ISSN 1463-9076 R&D Projects: GA ČR GA14-14082S; GA ČR GA14-08937S Institutional support: RVO:61388955 Keywords : POTENTIAL-ENERGY SURFACES * METHYL MERCAPTAN * CONICAL INTERSECTIONS Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.449, year: 2015

Electrochemical generation of fentons reagent to treat spent caustic wastewater

International Nuclear Information System (INIS)

Hansen, H. K.; Nunez, P.; Rodriguez, N.; Guzman, J.

2009-01-01

An important wastewater stream from oil refineries is the spent caustic. Caustic solutions are used as scrubbing agent during the desulphurization process to eliminate sulphur an mercaptans from oil and gasses. Spent caustic is classified as DOO3 (reactive sulphide) hazardous waste under the US Resource Conservation and Recovery Act (RCRA). (Author)

Methane oxidation and attenuation of sulphur compounds in landfill top cover systems: Lab-scale tests.

Science.gov (United States)

Raga, Roberto; Pivato, Alberto; Lavagnolo, Maria Cristina; Megido, Laura; Cossu, Raffaello

2018-03-01

In this study, a top cover system is investigated as a control for emissions during the aftercare of new landfills and for old landfills where biogas energy production might not be profitable. Different materials were studied as landfill cover system in lab-scale columns: mechanical-biological pretreated municipal solid waste (MBP); mechanical-biological pretreated biowaste (PB); fine (PBS f ) and coarse (PBS c ) mechanical-biological pretreated mixtures of biowaste and sewage sludge, and natural soil (NS). The effectiveness of these materials in removing methane and sulphur compounds from a gas stream was tested, even coupled with activated carbon membranes. Concentrations of CO 2 , CH 4 , O 2 , N 2 , H 2 S and mercaptans were analysed at different depths along the columns. Methane degradation was assessed using mass balance and the results were expressed in terms of methane oxidation rate (MOR). The highest maximum and mean MOR were observed for MBP (17.2gCH 4 /m 2 /hr and 10.3gCH 4 /m 2 /hr, respectively). Similar values were obtained with PB and PBS c . The lowest values of MOR were obtained for NS (6.7gCH 4 /m 2 /hr) and PBS f (3.6gCH 4 /m 2 /hr), which may be due to their low organic content and void index, respectively. Activated membranes with high load capacity did not seem to have an influence on the methane oxidation process: MBP coupled with 220g/m 2 and 360g/m 2 membranes gave maximum MOR of 16.5gCH 4 /m 2 /hr and 17.4gCH 4 /m 2 /hr, respectively. Activated carbon membranes proved to be very effective on H 2 S adsorption. Furthermore, carbonyl sulphide, ethyl mercaptan and isopropyl mercaptan seemed to be easily absorbed by the filling materials. Copyright © 2017. Published by Elsevier B.V.

Linear dimensional changes in plaster die models using different elastomeric materials

Directory of Open Access Journals (Sweden)

Jefferson Ricardo Pereira

2010-09-01

Full Text Available Dental impression is an important step in the preparation of prostheses since it provides the reproduction of anatomic and surface details of teeth and adjacent structures. The objective of this study was to evaluate the linear dimensional alterations in gypsum dies obtained with different elastomeric materials, using a resin coping impression technique with individual shells. A master cast made of stainless steel with fixed prosthesis characteristics with two prepared abutment teeth was used to obtain the impressions. References points (A, B, C, D, E and F were recorded on the occlusal and buccal surfaces of abutments to register the distances. The impressions were obtained using the following materials: polyether, mercaptan-polysulfide, addition silicone, and condensation silicone. The transfer impressions were made with custom trays and an irreversible hydrocolloid material and were poured with type IV gypsum. The distances between identified points in gypsum dies were measured using an optical microscope and the results were statistically analyzed by ANOVA (p < 0.05 and Tukey's test. The mean of the distances were registered as follows: addition silicone (AB = 13.6 µm, CD=15.0 µm, EF = 14.6 µm, GH=15.2 µm, mercaptan-polysulfide (AB = 36.0 µm, CD = 36.0 µm, EF = 39.6 µm, GH = 40.6 µm, polyether (AB = 35.2 µm, CD = 35.6 µm, EF = 39.4 µm, GH = 41.4 µm and condensation silicone (AB = 69.2 µm, CD = 71.0 µm, EF = 80.6 µm, GH = 81.2 µm. All of the measurements found in gypsum dies were compared to those of a master cast. The results demonstrated that the addition silicone provides the best stability of the compounds tested, followed by polyether, polysulfide and condensation silicone. No statistical differences were obtained between polyether and mercaptan-polysulfide materials.

Radiation method of sulfide compound transformation in petroleum products

International Nuclear Information System (INIS)

Nadirov, N.K.; Zajkina, R.F.; Zajkin, Yu.A.; Mamonova, T.B.; Bakirova, S.F.

1997-01-01

Processes of sulphuric compounds transformation for petroleum and heavy residuals under radiation and thermal treatment action are studied. It is shown that sulphuric compounds are concentrated in heavy fractions as a result of radiation processing. Heavy petroleum products irradiation provokes considerable decrease in the content of mercaptans, disulphides and sulphides, which transfer to sulphoxides and sulphones appearing during radiation-induced oxidation process. (author)

Effect of Selected Mercapto Flavor Compounds on Acrylamide Elimination in a Model System

Directory of Open Access Journals (Sweden)

Zhiyong Xiong

2017-05-01

Full Text Available The effect of four mercapto flavor compounds (1,2-ethanedithiol, 1-butanethiol, 2-methyl-3-furanthiol, and 2-furanmethanethiol on acrylamide elimination were investigated in model systems. The obtained results showed that mercaptans assayed were effective in elimination arylamide in a model system. Their reactivities for decreasing acrylamide content depended on mercaptan’s molecular structure and acrylamide disappearance decreased in the following order: 1,2-ethanedithiol > 2-methyl-3-furanthiol > 1-butanethiol > 2-furanmethanethiol. Mercaptans were added to acrylamide to produce the corresponding 3-(alkylthio propionamides. This reaction was irreversible and only trace amounts of acrylamide were formed by thermal heating of 3-(alkylthio propanamide. Although a large amount disappeared, only part of the acrylamide conversed into 3-(alkylthio propionamides. All of these results constitute a fundamental proof of the complexity of the reactions involved in the removal of free acrylamide in foods. This implies mercapto flavor/aroma may directly or indirectly reduce the level of acrylamide in food processing. This study could be regarded as a pioneer contribution on acrylamide elimination in a model system by the addition of mercapto flavor compounds.

Efficacy of a novel biofilter in hatchery sanitation: II. Removal of odorogenous pollutants.

Science.gov (United States)

Tymczyna, Leszek; Chmielowiec-Korzeniowska, Anna; Drabik, Agata; Skórska, Czesława; Sitkowska, Jolanta; Cholewa, Grazyna; Dutkiewicz, Jacek

2007-01-01

The present research assessed the treatment efficiency of odorogenous pollutants in air from a hatchery hall vented on organic and organic-mineral beds of an enclosed-container biofilter. In this study, the following media were used: organic medium containing compost and peat (OM); organic-mineral medium containing bentonite, compost and peat (BM); organic-mineral medium containing halloysite, compost and peat (HM). The concentration of odorogenous gaseous pollutants (sulfur compounds and amines) in the hatching room air and in the air after biotreatment were determined by gas chromatography. In the hatchery hall among the typical odorogenous pollutants, there were determined 2 amines: 2-butanamine and 2-pentanamine, hydrogen sulfide, sulfur dioxide, carbon disulfide, sulfides and mercaptans. Ethyl mercaptan showed the highest levels as its mean concentration in the hatchery hall air exceeded 60 microg/m3 and in single samples even 800 microg/m3. A mean concentration of 2-butanamine and sulfur dioxide in the examined air also appeared to be relatively high--21.405 microg/m3 and 15.279 microg/m3, respectively. In each filter material, the air treatment process ran in a different mode. As the comparison reveals, the mean reduction of odorogenous contaminants recorded in the hall and subjected to biotreatment was satisfying as it surpassed 60% for most established pollutants. These high removal values were confirmed statistically only for single compounds. However, a low removal level was reported for hydrogen sulfide and sulfur dioxide. No reduction was recorded in the bentonite supplemented medium (BM) for sulfur dioxide and methyl mercaptan. In the organic medium (OM) no concentration fall was noted for dipropyl sulfide either. In all the media investigated, the highest removal rate (100%), not confirmed statistically, was observed for carbon disulfide. Very good results were obtained in the medium with a bentonite additive (BM) for both identified amines, whose

Problem of air pollution

Energy Technology Data Exchange (ETDEWEB)

Berge, H

1964-01-01

The effects of air pollutants on plants are dependent on and modified by climatic, orographic, edaphic, and biotic factors; the synergism of pollutants; and differences in the sensitivity of individual plants and species. Sulfur dioxide and fluorine are the most dangerous pollutants for plants, but ammonia, hydrogen sulfide, nitrogen oxides, nitric acid, chlorine, hydrochloric acid, bromine, iodine, hydrocyanic acid, ethylene, carbon monoxide, hydrocarbons, mercaptans, asphalt and tar vapors, mercury, and selenium can also inflict damage. Young leaves, sensitive to H/sub 2/S, nitrogen oxides, Cl, HCl, HCN, mercaptans, Hg, and sulfuric acid, are more resistant to SO/sub 2/, gaseous F compounds, ethylene, and selenium than older leaves. Damage is most serious when pollutants enter leaves simultaneously or alternately through epidermis and stomata. The yellow-to-brown coloration of leaves is usually a result of the precipitation of tanning. Plasmolysis is caused by SO/sub 2/, gaseous F compounds, ammonia, nitrogen oxides, HNO/sub 3/, Br, asphalt and tar vapors, while photosynthesis is stimulated by traces of ammonia, HNO/sub 3/, and saturated hydrocarbons. Increased transpiration due to SO/sub 2/ and HCl and elevated permeability and osmosis due to SO/sub 2/ were observed. 9 references, 12 figures, 1 table.

Nickel-Catalyzed C-S Bond Formation via Decarbonylative Thioetherification of Esters, Amides and Intramolecular Recombination Fragment Coupling of Thioesters

KAUST Repository

Lee, Shao-Chi

2018-01-15

A nickel catalyzed cross-coupling protocol for the straightforward C-S bond formation has been developed. Various mercaptans and a wide range of ester and amide substrates bearing various substituents were tolerated in this process which afforded products in good to excellent yields. Furthermore, an intramolecular protocol for the synthesis of thioethers starting from thioesters has been developed. The utility of this protocol has been demonstrated in the synthesis of benzothiophene on the bench top.

Nickel-Catalyzed C-S Bond Formation via Decarbonylative Thioetherification of Esters, Amides and Intramolecular Recombination Fragment Coupling of Thioesters

KAUST Repository

Lee, Shao-Chi; Liao, Hsuan-Hung; Chatupheeraphat, Adisak; Rueping, Magnus

2018-01-01

A nickel catalyzed cross-coupling protocol for the straightforward C-S bond formation has been developed. Various mercaptans and a wide range of ester and amide substrates bearing various substituents were tolerated in this process which afforded products in good to excellent yields. Furthermore, an intramolecular protocol for the synthesis of thioethers starting from thioesters has been developed. The utility of this protocol has been demonstrated in the synthesis of benzothiophene on the bench top.

Natural sources of gaseous pollutants in the atmosphere

Energy Technology Data Exchange (ETDEWEB)

Altshuller, A P

1958-01-01

Various gaseous pollutants including ozone, nitrous oxide, nitric oxide, nitrogen dioxide, methane, hydrogen, formaldehyde, ammonia, hydrogen sulfide, mercaptans, chlorine compounds and free radicals can be formed by natural processes such as ultraviolet photochemical processes in the upper atmosphere and microbiological processes. The modes of formation and destruction of these gases, especially of their concentrations in the atmosphere, and the various reactions in which these gases can participate with each other are discussed in detail. 114 references.

Methylation of food commodities during fumigation with methyl bromide

International Nuclear Information System (INIS)

Starratt, A.N.; Bond, E.J.

1990-01-01

Sites of methylation in several commodities (wheat, oatmeal, peanuts, almonds, apples, oranges, maize, alfalfa and potatoes) during fumigation with 14 C-methyl bromide were studied. Differences were observed in levels of the major volatiles: methanol, dimethyl sulphide and methyl mercaptan, products of O- and S-methylation, resulting from treatment of the fumigated materials with 1N sodium hydroxide. In studies of maize and wheat, histidine was the amino acid which underwent the highest level of N-methylation. (author). 24 refs, 3 tabs

Action of Mercaptan and Disulfide in Hydrogen Atom Exchange Reactions; Action des Thioalcools et des Disulfures dans les Reactions d'Echange d'Atomes d'Hydrogene; Vozdejstvie merkaptanov i disul'fidov v reaktsiyakh obmena atoma vodoroda; Accion de los Mercaptanos y Disulfuros en las Reacciones de Intercambio del Hidrogeno Atomico

Energy Technology Data Exchange (ETDEWEB)

Cohen, S. G. [Brandeis University Waltham, MA (United States)

1965-10-15

Free- radical, photochemical, and high-energy radiation-induced reactions may be catalysed or inhibited by rapid hydrogen atom exchange reactions of mercaptans and disulfides. The radical-induced, light-initiated, and benzophenone-sensitized decarbonylations of aldehydes are catalysed by mercaptans. The chain-propagating hydrogen transfer reaction, R' + RCH = O -> RH + RC = O , is made more rapid by a similar sequence of hydrogen atom transfers involving the sulfur compound: R' + C{sub 6}H{sub 5}CH{sub 2}SH -> RH + C{sub 6}H{sub 5}CH{sub 2}S'; C{sub 6}H{sub 5}CH{sub 2}S + RCH = 0 -> C{sub 6}H{sub 5}CH{sub 2}SH + RC = 0. The photoreduction of benzophenone in 2-propanol leads to benzpinacol by a non-chain reaction via the radicals (C{sub 6}H{sub 5}){sub 2}C-OH and (CH{sub 3}){sub 2}COH. The reaction is retarded and inhibited by mercaptan and disulfide, which reconvert the radicals to the starting materials by rapid hydrogen transfer reactions and are themselves regenerated in their alternate valence states, each molecule of sulfur compound negating the chemical consequences of many quanta: (C{sub 6}H{sub 5}){sub 2}C-OH + AS' -> (C{sub 6}H{sub 5}){sub 2}C = O + ASH; (CH{sub 3}){sub 2}C-OH + ASH -> (CH{sub 3}){sub 2}C = 0 + AS'. Proof of the mechanism is found in: equilibration of initially present mercaptan or disulfide during inhibition; in racemization of optically active alcohol during inhibition; in deuterium exchange during inhibition. Similar inhibition is seen when only one intermediate radical is formed, as in the benzophenone- benzhydrol and acetophenone-{alpha}-methyl-benzyl alcohol systems. Inhibition by sulfur compounds, by the same mechanism, is found in the {sup 60}Co {gamma}-ray induced conversion of benzophenone to benzpinacol; naphthalene has no protecting effect on benzophenone in the {sup 60}Co system, while quenching the photochemical reaction. The protection by sulfur compounds of solutes against radiation damage thus results from hydrogen atom

Synthesis and Odor Evaluation of Five New Sulfur-Containing Ester Flavor Compounds from 4-Ethyloctanoic Acid

Directory of Open Access Journals (Sweden)

Baoguo Sun

2010-07-01

Full Text Available Five sulfur-containing flavor compounds were synthesized for the first time by the reaction of 4-ethyloctanoyl chloride with sulfur-containing alcohols or mercaptans. The synthesized compounds are 3-(methylthiopropyl 4-ethyloctanoate, 2-methyl-3-tetrahydro-furanthiol 4-ethyloctanoate, 4-methyl-5-thiazoleethanol 4-ethyloctanoate, 2-furan-methanethiol 4-ethyloctanoate and 2-methyl-3-furanthiol 4-ethyloctanoate. These five synthetic sulfur-containing ester flavor compounds all have meaty odor and might be used in foods if approved for this purpose in the future.

Synthesis and odor evaluation of five new sulfur-containing ester flavor compounds from 4-ethyloctanoic acid.

Science.gov (United States)

Liu, Yuping; Chen, Haitao; Yin, Decai; Sun, Baoguo

2010-07-29

Five sulfur-containing flavor compounds were synthesized for the first time by the reaction of 4-ethyloctanoyl chloride with sulfur-containing alcohols or mercaptans. The synthesized compounds are 3-(methylthio)propyl 4-ethyloctanoate, 2-methyl-3-tetrahydro-furanthiol 4-ethyloctanoate, 4-methyl-5-thiazoleethanol 4-ethyloctanoate, 2-furan-methanethiol 4-ethyloctanoate and 2-methyl-3-furanthiol 4-ethyloctanoate. These five synthetic sulfur-containing ester flavor compounds all have meaty odor and might be used in foods if approved for this purpose in the future.

The application of PS printing plate with Biimidazole photosensitive initiating systems

International Nuclear Information System (INIS)

Li Lidong; Xu Jinqi; Gao Fang; Yang Yongyuan

1999-01-01

The ultraviolet photosensitive initiating system is composed of 4,4'-bis(N,N'-dimethyl-amino)benzophenone(MK), 2-chlorohexaarylbiimidazole(o-C1-HABI) and a hydrogen donor co-initiator n-dodecyl mercaptan(SH). Under the irradiation by high pressure mercury lamp, the relationship between the photo-polymerization rate of MMA and the concentration of each component of the system, including MK, o-C1-HABI and SH, was studied. The excellent results have been obtained through studying the system's application on PS lithographic printing plate

Testing odorants recovery from a novel metallized fluorinated ethylene propylene gas sampling bag.

Science.gov (United States)

Zhu, Wenda; Koziel, Jacek A; Cai, Lingshuang; Wright, Donald; Kuhrt, Fred

2015-12-01

Industry-standard Tedlar bags for odor sample collection from confined animal feeding operations (CAFOs) have been challenged by the evidence of volatile organic compound (VOC) losses and background interferences. Novel impermeable aluminum foil with a thin layer of fluorinated ethylene propylene (FEP) film on the surface that is in contact with a gas sample was developed to address this challenge. In this research, Tedlar and metallized FEP bags were compared for (a) recoveries of four characteristic CAFO odorous VOCs (ethyl mercaptan, butyric acid, isovaleric acid and p-cresol) after 30 min and 24 hr sample storage time and for (b) chemical background interferences. All air sampling and analyses were performed with solid-phase microextraction (SPME) followed by gas chromatography-mass spectroscopy (GC-MS). Mean target gas sample recoveries from metallized FEP bags were 25.9% and 28.0% higher than those in Tedlar bags, for 30 min and 24 hr, respectively. Metallized FEP bags demonstrated the highest p-cresol recoveries after 30-min and 24-hr storage, 96.1±44.5% and 44.8±10.2%, respectively, among different types of sampling bags reported in previous studies. However, a higher variability was observed for p-cresol recovery with metallized FEP bags. A 0% recovery of ethyl mercaptan was observed with Tedlar bags after 24-hr storage, whereas an 85.7±7.4% recovery was achieved with metallized FEP bags. Recoveries of butyric and isovaleric acids were similar for both bag types. Two major impurities in Tedlar bags' background were identified as N,N-dimethylacetamide and phenol, while backgrounds of metallized FEP bags were significantly cleaner. Reusability of metallized FEP bags was tested. Caution is advised when using polymeric materials for storage of livestock-relevant odorous volatile organic compounds. The odorants loss with storage time confirmed that long-term storage in whole-air form is ill advised. A focused short-term odor sample containment should be

Quantitative analysis of sulfur forms of coal and the pyrolysis behavior of sulfur compounds; Sekitanchu no io kagobutsu no keitaibetsu gan`yuryo no teiryo to sono netsubunkai kyodo

Energy Technology Data Exchange (ETDEWEB)

Mae, K.; Miura, K.; Shimada, M. [Kyoto University, Kyoto (Japan). Faculty of Engineering

1996-10-28

As part of the studies on coal utilization basics, considerations were given on quantification of sulfur forms of coal and the pyrolysis behavior of sulfur compounds. With the temperature raising oxidation method, a thermo-balance was connected directly to a mass analyzer, and the coal temperature was raised at a rate of 5{degree}C per minute and gasified. Peak division was performed on SO2 and COS production to derive sulfur forms of coal. Using the slow-speed pyrolysis method, production rates of H2S, COS, SO2 and mercaptans were measured at a temperature raising rate of 20{degree}C per minute. Sulfur content in char was also measured. With the quick pyrolysis method, a Curie point pyrolyzer was connected directly to a gas chromatograph, by which secondary reaction is suppressed, and initial pyrolytic behavior can be tracked. All kinds of coals produce a considerable amount of SO2 in the slow-speed pyrolysis, but very little in the quick pyrolysis. Instead, H2S and mercaptans are produced. Sulfur compound producing mechanisms vary depending on the temperature raising rates. By using a parallel primary reaction model, analysis was made on reactions of H2S production based on different activation energies, such as those generated from pyrite decomposition and organic sulfur decomposition. The analytic result agreed also with that from the temperature raising oxidation method. 4 refs., 6 figs., 1 tab.

Stereospecific polymerization of acrylonitrile using acrylonitrile-urea canal complex initiated by γ-ray irradiation

International Nuclear Information System (INIS)

Yamazaki, Hitoshi; Miyazaki, Yukio; Kamide, Kenji

1991-01-01

An attempt was made to clarify the effect of polymerization conditions (e.g., the content of chain transfer reagent, irradiation dose, acrylonitrile (AN)-urea ratio, aging time) on the stereoregularity, the viscosity-average molecular weight M ν , and the conversion in the radiation-induced polymerization of AN-urea canal complex in the presence of radical chain transfer reagent including alkyl mercaptans, alkylamines, alkyl alcohols and chloroform. The addition of n-butyl mercaptan (n-BM) to AN-urea system slowed down the rate of the canal complex formation and decreased the amount of the canal complexes formed. The role of n-BM on the formation of AN-urea canal complex was also examined by DSC. The enthalpy of fusion (ΔH) of AN solid in AN-n-BM-urea system decreased with elapse of aging time, although ΔH of n-BM was almost constant in the whole range of aging time. From these findings, it was concluded that n-BM is not included in the AN-urea canal complex. The conversion decreased remarkably with an increase in n-BM content. When 2 mol%/AN of n-BM was added to AN, M ν was almost constant (ca. M ν = 2.0 x 10 5 ), irrespective of the amount of n-BM added. Addition of n-BM to AN-urea system brings about a small, but significant increase in the content of isotactic triad (mm) by 5 to 14%. (author)

Preparation of sup 125 I-creatine phosphokinase-MM

Energy Technology Data Exchange (ETDEWEB)

Jingxian, Su; Jingmin, Ma [Academia Sinica, Beijing, BJ (China). Inst. of Atomic Energy

1988-09-01

{sup 125}I-creatine phosphokinase-MM ({sup 125}I-CPK-MM) was prepared by {sup 125}I-labelled Bolton-Hunter reagent (HPNS). Iodinating conditions of HPNS and its conjugation to protein were studied. {sup 125}I-CPK-MM with immune activity was obtained and used to establish the {sup 125}I-CPK-MM radioimmunoassay method by the General Hospital of PLA. {sup 125}I-CPK-MM in PBS-G solution containing 0.015 mol/l ethyl mercaptan at 4-10 deg C can be used for one month.

Emissions and emission reduction systems in the coal derivative production facilities of a coking plant. Emissionsquellen in Kohlenwertstoffbetrieben von Kokereien und Massnahmen zu ihrer Verminderung

Energy Technology Data Exchange (ETDEWEB)

1985-01-01

Coking plants may present odour unisances to their vicinity although these odours are no health problem. Typical odorants emitted by a coking plant are: Hydrogen sulfide, mercaptanes, carbon sulfide, naphthaline, phenol and ammonia. The odour threshold of these substances may be quite close to the analytical detection limit. There are a large number of emission sources, e.g. production and storage containers, baths, tar sinks, and ventilation systems. The report describes the possible sources of emissions as well as the countermeasures available at the present state of the art.

Project Summary: Increased Fuel Affordability Through Deployable Refining Technology (Briefing Charts)

Science.gov (United States)

2016-05-01

Mercaptans (Thiols) The presence of sulfur in fuels leads to many detrimental effects: • Coking on rocket engine injector plates • Deposit formation in...resulting in a fairly complex chromatogram Typical chromatogram of RP1 rocket fuel Instrument conditions followed were from ASTM D 5623 Peak area vs...2 ] + RT ln (V1/ V2 ) K = C0,2 / CO,1 Partition coefficient RT ln K = V0( D1-02 – D2-02 ) + RT ln (V1/ V2 ) Di-0 is the distance in “solubility

Effects of mix ratio, moisture content and aeration rate on sulfur odor emissions during pig manure composting.

Science.gov (United States)

Zang, Bing; Li, Shuyan; Michel, Frederick; Li, Guoxue; Luo, Yuan; Zhang, Difang; Li, Yangyang

2016-10-01

Sulfur compounds in swine manure can cause odor emissions during composting if conditions are not conducive to their rapid oxidation and degradation. In this study, the effects of controllable composting process variables on sulfur odor emissions were investigated. These included pig manure to corn stalk mix ratio (0.7:1, 1.5:1 and 2.2:1dw basis), initial moisture content (60%, 65%, 70% and 75%) and aeration rate (1.0, 2.0, 3.0 and 4.0m(3)m(-3)h(-1)). The compounds measured were carbonyl sulfide, carbon disulfide, hydrogen sulfide, methyl mercaptan, ethyl mercaptan, diethyl sulfide, dimethyl sulfide (Me2S) and dimethyl disulfide (Me2SS). The results showed that total sulfur losses ranged from 3.9% to 18.3% after 26days of composting. Me2S and Me2SS were the primary (>59.61%) sulfur compounds released during this period. After turning, emission rates of both Me2S and Me2SS increased. Emissions of the other six sulfur compounds were low and inconsistent during composting. Within the compost, feedstock mix ratio significantly influenced the concentration of Me2SS, while aeration rate significantly affected Me2S concentration (pMoisture content did not have a significant effect on the concentrations of either of these two compounds. Concentrations of sulfur odor compounds were the lowest at the highest aeration rate. Therefore, high aeration rates during the thermophilic phase, especially after turning, are recommended to minimize sulfur odors produced during swine manure composting. Copyright © 2016 Elsevier Ltd. All rights reserved.

Sensing sulfur oxides and other sulfur bearing pollutants with solid electrolyte pellets. I. Gas concentration cells

Energy Technology Data Exchange (ETDEWEB)

Chamberland, A M; Gauthier, J M

1977-01-01

A new sensing technique using a solid electrolyte has been demonstrated for sulfur-bearing pollutants. Based on potentiometric measurements across a pellet of potassium sulfate, this sensor allows concentrations of sulfur dioxides, sulfur trioxide, hydrogen sulfide, methyl mercaptan and carbonyl sulfide in air to be measured with accuracy. Its operational concentration range at the present time is 0.1 ppM up to at least 10,000 ppM. The presence of other common pollutants such as carbon dioxide, methane, nitric oxide and nitrogen dioxide does not interfere with the measurement of air samples containing sulfur-bearing pollutants.

Potentiometric determination of trace amounts of volatile thiols in natural gas

International Nuclear Information System (INIS)

Farroha, S.M.; Habboush, A.E.; Kurthab, S.Y.

1986-01-01

A potentiometric titration method was developed for the determination of volatile thiols in natural gas. An apparatus was devised for the quantitative absorption of volatile thiols. The measurements were performed in an ethanolic ammonium buffer solution containing a known amount of silver nitrate as supporting electrolyte. The excess silver was precipitated by a known amount of potassium iodide. The excess of iodide was back titrated potentiometrically with a standard solution of silver nitrate. The direct titration of the excess silver ions with a standard solution of potassium iodide gave a poor accuracy compared with the back titration method. Iodide selective electrode was employed as an indicator electrode and a silver-silver chloride electrode as reference electrode. The accuracy and reproducibility of the method were established by preparing several synthetic samples in which ethanthiol containing from 346.61 to 12.11 μUg mercaptan sulfur was taken as standard nitrogen as carrier gas with an optimum flow rate of 31.5 L/hr. The results obtained expressed in the form of Grans plot showed an error ranging from 0.16 to 2.39% by weight and the relative standard deviation did not exceed 2.20%. The amount of mercaptan sulfur determined in Iraqi natural gas taken directly in a cylinder from Dora refinery, Baghdad, Iraq, and after six months of storage we 23.15 Ug/L and 21.25 Ug/L respectively with a relative standard deviation not exceeded 1%. The interferences of hydrogen sulfide could be eliminated by absorption in cadimium acetate containing solution. Other sulfur containing compounds e.g. disulfides, sulfoxides which may be present in natural gas do not interfere with the analysis

Seeded emulsion polymerization of butadiene. 2. Effects of persulfate and tert-dodecyl mercaptan

NARCIS (Netherlands)

Verdurmen, E.M.F.J.; Geurts, J.M.; Verstegen, J.M.; Maxwell, I.A.; German, A.L.

1993-01-01

The kinetics of the emulsion polymn. of butadiene at 60 Deg in Smith-Ewart interval III were investigated using sodium persulfate as initiator. Monomer conversion was based on gravimetrically calibrated online densitometry. Plots of the product of the propagation rate coeff., Kp, and the av. no. of

A method for removing sulfur bearing compounds from paraffinous hydrocarbons or a directly distilled benzine fraction

Energy Technology Data Exchange (ETDEWEB)

Konyukhova, T.P.; Bolotskaya, I.A.; Mikhaylova, L.A.; Sadykov, A.N.; Shitovkin, N.T.; Vlasov, V.V.

1983-01-01

In the known method for removing sulfurorganic compounds from paraffinous hydrocarbons or a directly distilled gasoline fraction through their adsorption using natural zeolite, in order to increase the degree of purification, clinoptilolite (Kp), which contains SiO2 and A12O3 in a molar ratio of 10.6 to 16.7 is used as the natural zeolite. The purification of the paraffinous hydrocarbons through clinoptilolite adsorption as compared with mordenite adsorption makes it possible to increase the degree of their purification of ethylmercaptane and dimethylsulfide. The effectiveness of clinoptilolite is also confirmed in removing mercaptanes and sulfides from directly distilled gasoline fractions.

Odor composition analysis and odor indicator selection during sewage sludge composting

Science.gov (United States)

Zhu, Yan-li; Zheng, Guo-di; Gao, Ding; Chen, Tong-bin; Wu, Fang-kun; Niu, Ming-jie; Zou, Ke-hua

2016-01-01

ABSTRACT On the basis of total temperature increase, normal dehydration, and maturity, the odor compositions of surface and internal piles in a well-run sewage sludge compost plant were analyzed using gas chromatography–mass spectrometry with a liquid nitrogen cooling system and a portable odor detector. Approximately 80 types of substances were detected, including 2 volatile inorganic compounds, 4 sulfur organic compounds, 16 benzenes, 27 alkanes, 15 alkenes, and 19 halogenated compounds. Most pollutants were mainly produced in the mesophilic and pre-thermophilic periods. The sulfur volatile organic compounds contributed significantly to odor and should be controlled primarily. Treatment strategies should be based on the properties of sulfur organic compounds. Hydrogen sulfide, methyl mercaptan, dimethyl disulfide, dimethyl sulfide, ammonia, and carbon disulfide were selected as core indicators. Ammonia, hydrogen sulfide, carbon disulfide, dimethyl disulfide, methyl mercaptan, dimethylbenzene, phenylpropane, and isopentane were designated as concentration indicators. Benzene, m-xylene, p-xylene, dimethylbenzene, dichloromethane, toluene, chlorobenzene, trichloromethane, carbon tetrachloride, and ethylbenzene were selected as health indicators. According to the principle of odor pollution indicator selection, dimethyl disulfide was selected as an odor pollution indicator of sewage sludge composting. Monitoring dimethyl disulfide provides a highly scientific method for modeling and evaluating odor pollution from sewage sludge composting facilities. Implications: Composting is one of the most important methods for sewage sludge treatment and improving the low organic matter content of many agricultural soils. However, odors are inevitably produced during the composting process. Understanding the production and emission patterns of odors is important for odor control and treatment. Core indicators, concentration indicators, and health indicators provide an index

Odor composition analysis and odor indicator selection during sewage sludge composting.

Science.gov (United States)

Zhu, Yan-Li; Zheng, Guo-di; Gao, Ding; Chen, Tong-Bin; Wu, Fang-Kun; Niu, Ming-Jie; Zou, Ke-Hua

2016-09-01

On the basis of total temperature increase, normal dehydration, and maturity, the odor compositions of surface and internal piles in a well-run sewage sludge compost plant were analyzed using gas chromatography-mass spectrometry with a liquid nitrogen cooling system and a portable odor detector. Approximately 80 types of substances were detected, including 2 volatile inorganic compounds, 4 sulfur organic compounds, 16 benzenes, 27 alkanes, 15 alkenes, and 19 halogenated compounds. Most pollutants were mainly produced in the mesophilic and pre-thermophilic periods. The sulfur volatile organic compounds contributed significantly to odor and should be controlled primarily. Treatment strategies should be based on the properties of sulfur organic compounds. Hydrogen sulfide, methyl mercaptan, dimethyl disulfide, dimethyl sulfide, ammonia, and carbon disulfide were selected as core indicators. Ammonia, hydrogen sulfide, carbon disulfide, dimethyl disulfide, methyl mercaptan, dimethylbenzene, phenylpropane, and isopentane were designated as concentration indicators. Benzene, m-xylene, p-xylene, dimethylbenzene, dichloromethane, toluene, chlorobenzene, trichloromethane, carbon tetrachloride, and ethylbenzene were selected as health indicators. According to the principle of odor pollution indicator selection, dimethyl disulfide was selected as an odor pollution indicator of sewage sludge composting. Monitoring dimethyl disulfide provides a highly scientific method for modeling and evaluating odor pollution from sewage sludge composting facilities. Composting is one of the most important methods for sewage sludge treatment and improving the low organic matter content of many agricultural soils. However, odors are inevitably produced during the composting process. Understanding the production and emission patterns of odors is important for odor control and treatment. Core indicators, concentration indicators, and health indicators provide an index system to odor evaluation

Infrared Spectra and Band Strengths of CH3SH, an Interstellar Molecule

Science.gov (United States)

Hudson, R. L.

2016-01-01

Three solid phases of CH3SH (methanethiol or methyl mercaptan) have been prepared and their mid-infrared spectra recorded at 10-110 degrees Kelvin, with an emphasis on the 17-100 degrees Kelvin region. Refractive indices have been measured at two temperatures and used to estimate ice densities and infrared band strengths. Vapor pressures for the two crystalline phases of CH3SH at 110 degrees Kelvin are estimated. The behavior of amorphous CH3SH on warming is presented and discussed in terms of Ostwald's step rule. Comparisons to CH3OH under similar conditions are made, and some inconsistencies and ambiguities in the CH3SH literature are examined and corrected.

Rapid labeling of amino acid neurotransmitters with a fluorescent thiol in the presence of o-phthalaldehyde.

Science.gov (United States)

Maddukuri, Naveen; Zhang, Qiyang; Zhang, Ning; Gong, Maojun

2017-02-01

LIF detection often requires labeling of analytes with fluorophores; and fast fluorescent derivatization is valuable for high-throughput analysis with flow-gated CE. Here, we report a fast fluorescein-labeling scheme for amino acid neurotransmitters, which were then rapidly separated and detected in flow-gated CE. This scheme was based on the reaction between primary amines and o-phthalaldehyde in the presence of a fluorescent thiol, 2-((5-fluoresceinyl)aminocarbonyl)ethyl mercaptan (FACE-SH). The short reaction time (neurotransmitters by coupling in vitro microdialysis with online derivatization and flow-gated CE. It is also anticipated that this fluorophore tagging scheme would be valuable for on-chip labeling of proteins retained on support in SPE. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

A method for eliminating sulfur compounds from fluid, saturated, aliphatic hydrocarbons

Energy Technology Data Exchange (ETDEWEB)

Fakhriev, A.M.; Galiautdinov, N.G.; Kashevarov, L.A.; Mazgarov, A.M.

1982-01-01

The method for eliminating sulfur compounds from fluid, saturated, aliphatic hydrocarbons, which involves extracting hydrocarbons using a dimethylsulfoxide extractant, is improved by using a dimethylsulfoxide blend and 10-60 percent (by volume) diethylenetriamine or polyethylenepolyamine which contains diethylenetriamine, triethylenetetramine and tetraethylenepentamine, in order to eliminate the above compounds. Polyethylenepolyamine is produced as a by-product during the production of ethylenediamine. Elimination is performed at 0-50 degrees and 1-60 atmospheres of pressure. Here, the extractant may contain up to 10 percent water. The use of the proposed method, rather than the existing method, will make it possible to increase hydrocarbon elimination from mercaptans by 40 percent and from H/sub 2/S by 10 percent when the same amount is eliminated from dialkylsulfides.

Protection of aliphatic alcohols by thiols

International Nuclear Information System (INIS)

Nanobashivili, E.M.; Chirakadze, G.G.; Panchvidze, M.V.; Gvilava, S.E.; Khidesheli, G.I.

1973-01-01

Study was made of methyl, ethyl, propyl, butyl and penthyl alcohols. The aqueous solutions of the alcohols were X-irradiated. Results are presented of the action of high-energy particles on the solutions of ethyl, propyl and butyl alcohols in the presence and absence of the minor amounts of ethanthiol. Protective effect of the -SH group was established. Addition of 1.10 -6 mol/1 of ethanthiol to butyl alcohol protects it completely against radiation conversions up to a dose of 8.10 19 eV/ml. Consideration is given to the effect of thioalcohol additives on the formation of some products of alcohol radiation oxidation. Introduction of mercaptans to the system or that of the -SH group to the organic compound molecule enhances its radiation resistance [ru

Getting sulfur on target

Energy Technology Data Exchange (ETDEWEB)

Halbert, T.R.; Brignac, G.B. [ExxonMobil Process Research Labs. (United States); Greeley, J.P.; Demmin, R.A.; Roundtree, E.M. [ExxonMobil Research and Engineering Co. (United States)

2000-06-01

The paper focuses on how the required reductions in sulfur levels in motor vehicle fuel may be achieved over about the next five years. It is said that broadly there are two possible approaches, they are: (a) to hydrotreat the feed to the FCC unit and (b) to treat the naphtha produced by the FCC unit. The difficulties associated with these processes are mentioned. The article is presented under the sub-headings of (i) technology options for cat naphtha desulfurisation; (ii) optimising fractionator design via improved VLE models; (iii) commercial experience with ICN SCANfining; (iv) mercaptan predictive models and (v) process improvements. It was concluded that the individual needs of the refiner can be addressed by ExxonMobil Research and Engineering (EMRE) and the necessary reductions in sulfur levels can be achieved.

A fuzzy logic approach to control anaerobic digestion.

Science.gov (United States)

Domnanovich, A M; Strik, D P; Zani, L; Pfeiffer, B; Karlovits, M; Braun, R; Holubar, P

2003-01-01

One of the goals of the EU-Project AMONCO (Advanced Prediction, Monitoring and Controlling of Anaerobic Digestion Process Behaviour towards Biogas Usage in Fuel Cells) is to create a control tool for the anaerobic digestion process, which predicts the volumetric organic loading rate (Bv) for the next day, to obtain a high biogas quality and production. The biogas should contain a high methane concentration (over 50%) and a low concentration of components toxic for fuel cells, e.g. hydrogen sulphide, siloxanes, ammonia and mercaptanes. For producing data to test the control tool, four 20 l anaerobic Continuously Stirred Tank Reactors (CSTR) are operated. For controlling two systems were investigated: a pure fuzzy logic system and a hybrid-system which contains a fuzzy based reactor condition calculation and a hierachial neural net in a cascade of optimisation algorithms.

Association models for petroleum applications

DEFF Research Database (Denmark)

Kontogeorgis, Georgios

2013-01-01

Thermodynamics plays an important role in many applications in the petroleum industry, both upstream and downstream, ranging from flow assurance, (enhanced) oil recovery and control of chemicals to meet production and environmental regulations. There are many different applications in the oil & gas...... industry, thus thermodynamic data (phase behaviour, densities, speed of sound, etc) are needed to study a very diverse range of compounds in addition to the petroleum ones (CO2, H2S, water, alcohols, glycols, mercaptans, mercury, asphaltenes, waxes, polymers, electrolytes, biofuels, etc) within a very....... Such association models have been, especially over the last 20 years, proved to be very successful in predicting many thermodynamic properties in the oil & gas industry. They have not so far replaced cubic equations of state, but the results obtained by using these models are very impressive in many cases, e...

Purifying oils, cracking oils, catalysts. [British Patent

Energy Technology Data Exchange (ETDEWEB)

1936-02-05

Hydrocarbon oils are refined by treating while substantially in the liquid phase between 200/sup 0/ and 400/sup 0/C with a phosphoric acid catalyst deposited on metallurgical coke, a suitable blast furnace slag, silica gel or other carrier with similar properties, until the objectionable components are converted into innocuous substances by polymerization cracking, isomerization and/or alkylation. By this treatment the bromine number is reduced, the end-point of the A.S.T.M. distillation is increased, the octane number is raised, mercaptans are converted to hydrogen sulphide and olefines, thioethers and thiophenes are converted to mereaptans, and the initial boiling point is lowered. The process is applicable to gasoline, cracked distillate, kerosine and lubricating oil, obtained by distilling or cracking petroleum, shale and hydrogenated oils; and is particularly applicable for stabilizing cracked distillates.

Syntheses of some Bunte's salts, isothiourea derivatives and thioethers, potential radioprotective agents. Part 40

International Nuclear Information System (INIS)

Tulecki, J.; Kalinowska Torz, J.; Musial, E.; Nacewicz-Anjedani, H.; Senczuk, L.; Skwarski, D.; Sobolewski, H.

1977-01-01

By reacting respective halogen-derivatives with sodium or potassium thiosulphate there were obtained sodium or potassium salts of S-thiosulphates of 1-ureidocarbonyl-1-butyl, 3,4-dihydroxyphenacyl, carbophenoxymethyl, 2-hydroxyphenacyl, /N-(4-iodophenyl) carbamyl/methyl, /N-(4-iodophenyl) carbamyl/ethyl, /N-(2-iodophenyl) carbamyl/-methyl, /N-(2-iodophenyl) carbamyl/ethyl, /N-(6-carbomethoxybenzothiazolyl-2)-carbamyl/methyl, (2,4-dihydroxy-6-methylpyrimidyl-5)-methyl and (2,4-dihydroxypyrimidyl-5)-methyl. Reactions of thiourea with respective halogen-derivatives yielded hydrochlorides of 1-methyl-02-amidinothiomethylbenzimidazole, 1-ethyl-2-amidinothiomethylbenzimidazole, S-/N-(2-iodophenyl) carbamylethyl/ isothiourea, 5-amidinothiomethyl-6-methyl-2,4-dihydroxypyrimide and 5-amidinothiomethyl-2,4-dihydroxypyrimidine. Reactions of 4-chloroquinoline N-oxide with respective mercaptanes afforded thioether derivatives of quinoline N-oxide: 4-(p-chlorophenylthio)-4-(t-butylthio)-, 4-(3-naphtylthio)-, 4-(3-naphtylaminoacetylthio), 4-(benzimidazolythio)-, 4-(benzothiazolylthio) - and 4-benzoxalylthio. (author)

Effect of the different chain transfer agents on molecular weight and optical properties of poly(methyl methacrylate)

Science.gov (United States)

Çetinkaya, Onur; Demirci, Gökhan; Mergo, Paweł

2017-08-01

Investigation of molecular weight and optical properties of poly(methyl metacrylate) (PMMA) polymerized in house with different chain transfer agents was studied. Isopropyl alcohol (IPA), n-butyl mercaptan (nBMC) and pentamethyl disilane (PMDS) were used as chain transfer agents. The molecular weight (Mw) of PMMA samples were measured by Ostwald viscometer. Mw of bulk polymer samples were decreased with increase the concentration of chain transfer agents (CTA). Since reactivity of used CTAs is not same, molecular weights of samples which were produced with different type of CTA but same concentration of CTA was varied. Higher concentration of n-BMC showed higher scattering. Transmission of samples could not be correlated with different concentration of CTA. Refractive index of samples was not affected by concentration of CTA nevertheless higher molecular weight of CTA showed higher refractive index.

Malodorous pollutants: a problem of public health

Energy Technology Data Exchange (ETDEWEB)

Muzzi, A; Tarsitani, G

1973-01-01

The mechanism of odor perception in humans, the toxic, physiological, and psychic effects of malodorous substances, and possible ways of controlling malodorous emissions are surveyed. While many malodorous substances are toxic, when present in concentrations above the odor threshold they may cause nuisance, nausea, anorexia, and sleeplessness. Malodorous emissions are generated in the pulp and paper, petroleum refinery, fertilizer, detergent, resin, fiber and rubber production, metallurgical, pharmaceutical, paint, and food industries and by automobiles. Acetaldehyde, acetic and butyric acids, acrolein, dimethyl, trimethyl and monomethyl amines, chlorine, dimethyl sulfur, ethylacrylate, ethylmercaptan, phenol, methyl mercaptan, nitrobenzene, paracresol, pyridine, and styrene are among the industrial malodorous substances with the lowest odor thresholds. The nuisances due to malodorous emissions can be avoided by diluting the malodorous substances prior to emission. In most cases, however, effective odor control by scrubbing, absorption, adsorption, filtration, thermal incineration, or oxidation with chlorine, permanganate, or ozone are required.

Production of sulfur gases and carbon dioxide by synthetic weathering of crushed drill cores from the Santa Cruz porphyry copper deposit near Casa Grande, Pinal County, Arizona

Science.gov (United States)

Hinkle, M.E.; Ryder, J.L.; Sutley, S.J.; Botinelly, T.

1990-01-01

Samples of ground drill cores from the southern part of the Santa Cruz porphyry copper deposit, Casa Grande, Arizona, were oxidized in simulated weathering experiments. The samples were also separated into various mineral fractions and analyzed for contents of metals and sulfide minerals. The principal sulfide mineral present was pyrite. Gases produced in the weathering experiments were measured by gas chromatography. Carbon dioxide, oxygen, carbonyl sulfide, sulfur dioxide and carbon disulfide were found in the gases; no hydrogen sulfide, organic sulfides, or mercaptans were detected. Oxygen concentration was very important for production of the volatiles measured; in general, oxygen concentration was more important to gas production than were metallic element content, sulfide mineral content, or mineral fraction (oxide or sulfide) of the sample. The various volatile species also appeared to be interactive; some of the volatiles measured may have been formed through gas reactions. ?? 1990.

A High-Yield Synthesis of Chalcopyrite CuInS2 Nanoparticles with Exceptional Size Control

Directory of Open Access Journals (Sweden)

Chivin Sun

2009-01-01

Full Text Available We report high-yield and efficient size-controlled syntheses of Chalcopyrite CuInS2 nanoparticles by decomposing molecular single source precursors (SSPs via microwave irradiation in the presence of 1,2-ethanedithiol at reaction temperatures as low as 100°C and times as short as 30 minutes. The nanoparticles sizes were 1.8 nm to 10.8 nm as reaction temperatures were varied from 100°C to 200°C with the bandgaps from 2.71 eV to 1.28 eV with good size control and high yields (64%–95%. The resulting nanoparticles were analyzed by XRD, UV-Vis, ICP-OES, XPS, SEM, EDS, and HRTEM. Titration studies by 1H NMR using SSP 1 with 1,2-ethanedithiol and benzyl mercaptan were conducted to elucidate the formation of Chalcopyrite CuInS2 nanoparticles.

Extended local similarity analysis (eLSA) reveals unique associations between bacterial community structure and odor emission during pig carcasses decomposition.

Science.gov (United States)

Ki, Bo-Min; Ryu, Hee Wook; Cho, Kyung-Suk

2018-02-22

Soil burial and composting methods have been widely used for the disposal of pig carcasses. The relationship between bacterial community structure and odor emission was examined using extended local similarity analysis (eLSA) during the degradation of pig carcasses in soil and compost. In soil, Hyphomicrobium, Niastella, Rhodanobacter, Polaromonas, Dokdonella and Mesorhizobium were associated with the emission of sulfur-containing odors such as hydrogen sulfide, methyl mercaptan and dimethyl disulfide. Sphingomonas, Rhodanobacter, Mesorhizobium, Dokdonella, Leucobacter and Truepera were associated with the emission of nitrogen-containing odors including ammonia and trimetylamine. In compost, however, Carnobacteriaceae, Lachnospiaceae and Clostridiales were highly correlated with the emission of sulfur-containing odors, while Rumincoccaceae was associated with the emission of nitrogen-containing odors. The emission of organic acids was closely related to Massilia, Sphaerobacter and Bradyrhizobiaceae in soil, but to Actinobacteria, Sporacetigenium, Micromonosporaceae and Solirubrobacteriales in compost. This study suggests that network analysis using eLSA is a useful strategy for exploring the mechanisms of odor emission during biodegradation of pig carcasses.

Biogas utilization

Energy Technology Data Exchange (ETDEWEB)

Moser, M.A. [Resource Conservation Management, Inc., Berkeley, CA (United States)

1996-01-01

Options for successfully using biogas depend on project scale. Almost all biogas from anaerobic digesters must first go through a gas handling system that pressurizes, meters, and filters the biogas. Additional treatment, including hydrogen sulfide-mercaptan scrubbing, gas drying, and carbon dioxide removal may be necessary for specialized uses, but these are complex and expensive processes. Thus, they can be justified only for large-scale projects that require high-quality biogas. Small-scale projects (less than 65 cfm) generally use biogas (as produced) as a boiler fuel or for fueling internal combustion engine-generators to produce electricity. If engines or boilers are selected properly, there should be no need to remove hydrogen sulfide. Small-scale combustion turbines, steam turbines, and fuel cells are not used because of their technical complexity and high capital cost. Biogas cleanup to pipeline or transportation fuel specifications is very costly, and energy economics preclude this level of treatment.

Iron sponge installation clicks at Retlaw plant

Energy Technology Data Exchange (ETDEWEB)

1965-06-21

Iron sponge desulfurization, often ignored by plant designers in favor of the monoethanolamine process, may offer economic advantages in sweetening of small gas volumes with low hydrogen sulfide and carbon dioxide content. The process removes hydrogen sulfide and mercaptans by passing sour gas through vessels loosely packed with wood shavings impregnated by a hydrated form of iron oxide, which reacts with the hydrogen sulfide to form ferric sulfide. The disadvantages are that carbon dioxide is not removed, hydrate formation is a danger in cold weather, and gas sales may be lost when towers are down for servicing. Periodic regeneration of beds takes about a day, and sponges must be replaced occasionally. Despite these shortcomings, the process may prove economical, since a typical plant costs $110,000 as compared to $270,000 for an amine unit. The expense of operating the plant is $23,000 compared with $28,000 for the amine unit. Thus, economics clearly favor the iron sponge process.

Lossless synthesis of graphene nanosheets decorated with tiny cadmium sulfide quantum dots with excellent nonlinear optical properties

International Nuclear Information System (INIS)

Feng Miao; Zhan Hongbing; Sun Ruiqing; Chen Yu

2010-01-01

The implantation and growth of metal nanoparticles on graphene nanosheets (GNS) leads directly to severe damage to the regular structure of the graphene sheets, which disrupts the extended π conjugation, resulting in an impaired device performance. In this paper, we describe a facile approach for achieving the lossless formation of graphene composite decorated with tiny cadmium sulfide quantum dots (QDs) with excellent nonlinear optical properties by using benzyl mercaptan (BM) as the interlinker. The mercapto substituent of BM binds to the CdS QDs during their nucleation and growth process, and then the phenyl comes into contact with the GNS via the π-π stacking interaction. Using this strategy, CdS QDs with an average diameter of 3 nm are uniformly dispersed over the surface of graphene, and the resulting QD-graphene composite exhibits excellent optical limiting properties, mainly contributed by nonlinear scattering and nonlinear absorption, upon both 532 and 1064 nm excitations, in the nanosecond laser pulse regime.

Inhibitory effect of Lactobacillus reuteri on periodontopathic and cariogenic bacteria.

Science.gov (United States)

Kang, Mi-Sun; Oh, Jong-Suk; Lee, Hyun-Chul; Lim, Hoi-Soon; Lee, Seok-Woo; Yang, Kyu-Ho; Choi, Nam-Ki; Kim, Seon-Mi

2011-04-01

The interaction between Lactobacillus reuteri, a probiotic bacterium, and oral pathogenic bacteria have not been studied adequately. This study examined the effects of L. reuteri on the proliferation of periodontopathic bacteria including Aggregatibacter actinomycetemcomitans, Fusobacterium nucleatum, Porphyromonas gingivalis, and Tannerella forsythia, and on the formation of Streptococcus mutans biofilms. Human-derived L. reuteri strains (KCTC 3594 and KCTC 3678) and rat-derived L. reuteri KCTC 3679 were used. All strains exhibited significant inhibitory effects on the growth of periodontopathic bacteria and the formation of S. mutans biofilms. These antibacterial activities of L. reuteri were attributed to the production of organic acids, hydrogen peroxide, and a bacteriocin-like compound. Reuterin, an antimicrobial factor, was produced only by L. reuteri KCTC 3594. In addition, L. reuteri inhibited the production of methyl mercaptan by F. nucleatum and P. gingivalis. Overall, these results suggest that L. reuteri may be useful as a probiotic agent for improving oral health.

Superhydrophobic Ag nanostructures on polyaniline membranes with strong SERS enhancement.

Science.gov (United States)

Liu, Weiyu; Miao, Peng; Xiong, Lu; Du, Yunchen; Han, Xijiang; Xu, Ping

2014-11-07

We demonstrate here a facile fabrication of n-dodecyl mercaptan-modified superhydrophobic Ag nanostructures on polyaniline membranes for molecular detection based on SERS technique, which combines the superhydrophobic condensation effect and the high enhancement factor. It is calculated that the as-fabricated superhydrophobic substrate can exhibit a 21-fold stronger molecular condensation, and thus further amplifies the SERS signal to achieve more sensitive detection. The detection limit of the target molecule, methylene blue (MB), on this superhydrophobic substrate can be 1 order of magnitude higher than that on the hydrophilic substrate. With high reproducibility, the feasibility of using this SERS-active superhydrophobic substrate for quantitative molecular detection is explored. A partial least squares (PLS) model was established for the quantification of MB by SERS, with correlation coefficient R(2) = 95.1% and root-mean-squared error of prediction (RMSEP) = 0.226. We believe this superhydrophobic SERS substrate can be widely used in trace analysis due to its facile fabrication, high signal reproducibility and promising SERS performance.

Polymeric redox-responsive delivery systems bearing ammonium salts cross-linked via disulfides

Directory of Open Access Journals (Sweden)

Christian Dollendorf

2013-08-01

Full Text Available A redox-responsive polycationic system was synthesized via copolymerization of N,N-diethylacrylamide (DEAAm and 2-(dimethylaminoethyl methacrylate (DMAEMA. N,N’-bis(4-chlorobutanoylcystamine was used as disulfide-containing cross-linker to form networks by the quaternization of tertiary amine groups. The insoluble cationic hydrogels become soluble by reduction of disulfide to mercaptanes by use of dithiothreitol (DTT, tris(2-carboxyethylphosphine (TCEP or cysteamine, respectively. The soluble polymeric system can be cross-linked again by using oxygen or hydrogen peroxide under basic conditions. The redox-responsive polymer networks can be used for molecular inclusion and controlled release. As an example, phenolphthalein, methylene blue and reactive orange 16 were included into the network. After treatment with DTT a release of the dye could be recognized. Physical properties of the cross-linked materials, e.g., glass transition temperature (Tg, swelling behavior and cloud points (Tc were investigated. Redox-responsive behavior was further analyzed by rheological measurements.

Chemistry of the organic-rich hot core G327.3-0.6

Science.gov (United States)

Gibb, E.; Nummelin, A.; Irvine, W. M.; Whittet, D. C.; Bergman, P.; Ferris, J. P. (Principal Investigator)

2000-01-01

We present gas-phase abundances of species found in the organic-rich hot core G327.3-0.6. The data were taken with the Swedish-ESO Submillimetre Telescope (SEST). The 1-3 mm spectrum of this source is dominated by emission features of nitrile species and saturated organics, with abundances greater than those found in many other hot cores, including Sgr B2 and OMC-1. Population diagram analysis indicates that many species (CH3CN, C2H3CN, C2H5CN, CH3OH, etc.) have hot components that originate in a compact (2") region. Gas-phase chemical models cannot reproduce the high abundances of these molecules found in hot cores, and we suggest that they originate from processing and evaporation of icy grain mantle material. In addition, we report the first detection of vibrationally excited ethyl cyanide and the first detection of methyl mercaptan (CH3SH) outside the Galactic center.

Effect of mouth cleaning with hinokitiol-containing gel on oral malodor: a randomized, open-label pilot study.

Science.gov (United States)

Iha, Kosaku; Suzuki, Nao; Yoneda, Masahiro; Takeshita, Toru; Hirofuji, Takao

2013-10-01

The aim of the study was to evaluate the effect of mouth cleaning with hinokitiol-containing gel on oral malodor. An open-label, randomized, controlled trial was conducted to assess oral malodor and clinical parameters related to oral malodor before and after mouth cleaning with hinokitiol-containing gel (n = 9) or with gel not including hinokitiol (n = 9). Mouth cleaning included the teeth, gingiva, and tongue and was carried out 3 times per day for 4 weeks. Organoleptic test (OLT) scores (P = .021), levels of hydrogen sulfide (P = .008) and methyl mercaptan (P = .020), frequency of bleeding on probing, average probing pocket depth, and plaque index significantly improved in the group using hinokitiol. In contrast, only the OLT score (P = .031) significantly improved in the control group after the treatment regimen. Mouth cleaning with hinokitiol-containing gel may be effective for reduction of oral malodor. Copyright © 2013 Elsevier Inc. All rights reserved.

Measurement of Henry’s Law constant and infinite dilution activity coefficient of isopropyl mercaptan and isobutyl mercaptan in (methyldiethanolamine (1) + water (2)) with w_1 = 0.25 and 0.50 at temperature of (298 to 348) K using inert gas stripping method

International Nuclear Information System (INIS)

Zin, Rohani Mohd; Coquelet, Christophe; Valtz, Alain; Abdul Mutalib, Mohamed I.; Sabil, Khalik Mohamad

2016-01-01

Highlights: • Measurement of Henry’s Law constants of nPM, iPM, nBM and iBM in aqueous MDEA. • Measurement of infinite dilution activity coefficients of nPM, iPM, nBM and iBM in aqueous MDEA. • Measurement using gas stripping method for T = (298 to 348) K and MDEA solution of (25 and 50) wt%. • Limiting activity coefficient and Henry’s Law constant is increasing with solute molecular size. • The experimental technique has provided information about heats of solution of aqueous MDEA. - Abstract: In this study, the Henry’s Law constant and the activity coefficients in infinite dilution in a mass fraction of (25 and 50)% of methyldiethanolamine (MDEA) aqueous solution within the temperature range of (298 to 348) K at atmospheric pressure, were measured. An inert gas stripping method was used to perform all the measurements. The new values of Henry’s Law constant and the activity coefficients in infinite dilution correlation with solute molecular size were explained. The influence of the solvent is discussed taking into consideration the heat of absorptions for different MDEA concentrations. Experimental results are compared to literature data wherever available.

A cutting fluid

Energy Technology Data Exchange (ETDEWEB)

Kajdas, C.; Dominiak, M.; Kozinski, R.; Misterkiewicz, B.; Polowniak, J.; Szczepaniak, S.

1982-06-30

The cutting fluid (SOZh) contains 0.5 to 10 percent vegetable or animal fats, selectively sulfurized in the presence of a catalyst (Kt): 0.1 to 10 percent chlorinated C2O to C3O paraffins, which contain 10 to 50 percent Chlorine in a molecule, and 0.001 to 0.5 percent dialkyldithiocarbamic or alkylen-bis-(dithiocarbamic) acids or their salts or derivatives of the form (R(R')NC(S)SRn'', (CH2)n(NHC(S)S)2R'' or R(R')NC(S)SnC(S)(R)R', where R and R' are alkyl or cycloalkyl of the C1 to C6 fractions, R'' is Hydrogen, a metal, or aliphatic or heterocyclic amine, n = 2 to 6 and 0.001 to 0.3 percent of heterocyclic mercaptanes or disulfides of the cited formula, where A is Nitrogen or Sulfur, and up to 100 percent petroleum oil with a kinematic viscosity of 5 to 50 square millimeters per second at 323K.

Use of Hg-Electroplated-Pt Ultramicroelectrode for Determining Elemental Sulphur in Naphtha Samples

Directory of Open Access Journals (Sweden)

Carlos Eduardo de Andrade

2012-01-01

Full Text Available This paper describes the applicability of a Hg-electroplated-Pt ultramicroelectrode in the quantification of elemental sulphur in naphtha samples by square-wave voltammetry. A reproducible deposition methodology was studied and is reported in this paper. This methodology is innovative and relies on the quality of the mercury stock solution to obtain reproducible surfaces required for the analytical methodology. All analyses were performed using a Hg-electroplated-Pt ultramicroelectrode (Hg-Pt UME due to the low sensibility of such devices to ohmic drops in resistive solutions. The responses of the peak areas in voltammetric experiments were linear in all of the range studied. The method developed here is accurate and reproducible, with a detection limit of 0.010 mg L−1 and a good recovery range for both standard solutions of elemental sulphur (85 to 99% and real naphtha sample (79%. These results attest to the potential for the application of this electroanalytical methodology in determining elemental sulphur in naphtha samples containing mercaptans and disulphides.

Efficacy of succimer chelation of mercury at background exposures in toddlers: a randomized trial

Science.gov (United States)

Cao, Yang; Chen, Aimin; Jones, Robert L.; Radcliffe, Jerilynn; Dietrich, Kim N.; Caldwell, Kathleen L.; Peddada, Shyamal; Rogan, Walter J.

2011-01-01

Objective To examine whether succimer, a mercaptan compound known to reduce blood lead concentration in children, reduces blood mercury concentration. Study Design We used samples from a randomized clinical trial of succimer chelation for lead-exposed children. We measured mercury in pre-treatment samples from 767 children. We also measured mercury in blood samples drawn 1 week after treatment began (N=768) and in a 20% random sample of the children who received the maximum 3 courses of treatment (N=67). A bootstrap-based isotonic regression method was used to compare the trend over time in the difference between the adjusted mean mercury concentrations in the succimer group and the placebo group. Results The adjusted mean organic mercury concentration in the succimer group relative to the placebo group fell from 99% at baseline to 82% after three courses of treatment (p for trend = 0.048), but this resulted from the prevention of the age-related increase in the succimer group. Conclusion Succimer chelation for low level organic mercury exposure in children has limited efficacy. PMID:20889164

Use of zeolites for the removal of volatile sulfur compounds from industrial waste gases and from natural gases

Energy Technology Data Exchange (ETDEWEB)

Dudzik,; Z,; Bilska, M

1974-12-01

The use of zeolites for the removal of sulfur dioxide from industrial waste gases and for the removal of hydrogen sulfide and volatile mercaptans from the natural gas or synthetic gas manufactured from coal is discussed. The effectiveness and cost of zeolite methods are superior to that of other methods. The best sorption properties with respect to sulfur dioxide are observed in faujasites and erionites. The molecular sieve 13X (a sodium form of low-silicon faujasite) is the most effective sorbent of hydrogen sulfide, produced commercially on a large scale. This zeolite is also a very effective catalyst for simultaneous oxygenation of hydrogen sulfide. The reaction with oxygen can begin at temperatures as low as -80/sup 0/C. The effectiveness of zeolite reactors is enhanced by the presence of oxygen in the gas being purified, and is hindered by the presence of water or water vapor. The extraordinary catalytic activity of sodium faujasites is due to free donors, and sulfur and oxygen ion donors at their surface. A zeolite reactor is also economical.

Single Stage Silicone Border Molded Closed Mouth Impression Technique-Part II.

Science.gov (United States)

Solomon, E G R

2011-09-01

Functioning of a complete denture depends to a great extent on the impression technique. Several impression techniques have been described in the literature since the turn of this century when Greene [Clinical courses in dental prothesis, 1916] brothers introduced the first scientific system of recording dental impression. Advocates of each technique have their own claim of superiority over the other. The introduction of elastomeric impression materials [Skinner and Cooper, J Am Dent Assoc 51:523-536, 1955] has made possible new techniques of recording impression for complete denture construction. These rubber like materials are of two types; one has a polysulfide base and is popularily known as polysulfide rubber (Thiokol and Mercaptan). The other variety has a silicone base known as silicone rubber or silicone elastomer. Silicone elastomers are available in four different consistencies; a thin easy flowing light bodied material,a creamy medium bodied material, a highly viscous heavy bodied material and a kneadable putty material. This paper describes an active closed mouth impression technique with one stage border molding using putty silicone material as a substitute for low fusing compound.

Halitosis: An oral microbial faction

Directory of Open Access Journals (Sweden)

Rajiv Saini

2010-01-01

Full Text Available Halitosis is a widespread condition and believed to affect one-quarter of the population around the world; also, most people have this condition from time to time. Breath malodour may be an important factor in social communication, and therefore may be the origin of concern not only for a possible health condition but also for frequent psychological alterations, leading to social and personal isolation. The most conspicuous malodorous compounds are termed volatile sulphur compounds (VSCs, with hydrogen sulphide, methyl mercaptan, and dimethyl sulphide accounting for roughly 90% of the VSCs. A number of oral bacteria, especially Gram-negative anaerobic species found in the subgingival plaque, produce a diverse array of malodorous compounds as byproducts of their metabolism, including VSCs and short-chain organic acids. Assessment and management of halitosis is of paramount importance in enhancing the overall health; moreover, dentists play a significant role in combating halitosis by reducing the oral microbial stack. Thus, the aim of the present review was to describe the aetiological factors, assessment tools, and therapeutic approaches related to halitosis.

Lessons learned from the Sullivan tragedy : a regulator's point of view

Energy Technology Data Exchange (ETDEWEB)

Hoffman, A. [British Columbia Ministry of Energy, Mines and Petroleum Resources, Victoria, BC (Canada). Mining and Minerals Div

2010-07-01

In May of 2006, inspectors from the British Columbia Health and Safety Branch responded to fatalities at a waste dump at Tech Cominco's Sullivan mine near Kimberley, British Columbia. Four persons died in the water monitoring shed. The immediate cause of the accident and its investigation were reviewed. Initial sampling using an electronic gas detector and probe showed depressed oxygen levels. There were no noticeable odours of hydrogen sulphide, sulphur dioxide or methyl mercaptan. Velocimetry readings indicated an inflow of air into the sump through the inlet pipe. Initial findings showed that the depleted oxygen levels were due to an oxidation of sulphidic waste rock that occurred upstream of the inlet drainage pipe inside the dump. A reaction of acid with carbonates in the waste dump rock generated high, but not lethal, carbon dioxide levels. This presentation reviewed the recommendations of the Sullivan Inquest Jury and the resulting changes in policy, and revisions to the Health, Safety and Reclamation Code for the province. 3 refs., 6 figs.

Fracture behaviour of a self-healing microcapsule-loaded epoxy system

Directory of Open Access Journals (Sweden)

2011-03-01

Full Text Available The effect of temperature on the fracture behaviour of a microcapsule-loaded epoxy matrix was investigated. Microencapsulated epoxy and mercaptan-derivative healing agents were incorporated into an epoxy matrix to produce a polymer composite capable of self-healing. Maximum fracture loads were measured using the double-torsion method. Thermal aging at 55 and 110°C for 17 hours [hrs] was applied to heal the pre-cracked samples. The addition of microcapsules appeared to increase significantly the load carrying capacity of the epoxy after healing. Once healed, the composites achieved as much as 93–171% of its virgin maximum fracture load at 18, 55 and 110°C. The fracture behavior of the microcapsule- loaded epoxy matrix was influenced by the healing temperature. The high self-healing efficiency may be attributed to the result of the subsurface micro-crack pinning or deviation, and to a stronger microencapsulated epoxy and mercaptanderivative binder than that of the bulk epoxy. The results show that the healing temperature has a significant effect on recovery of load transferring capability after fracture.

Photo-initiated polymerisation of 1,8-octanedithiol and styrene

International Nuclear Information System (INIS)

Ang, J.B.; Hill, D.J.T.; Pomery, P.J.; Whittaker, A.K.

1998-01-01

Full text: Photo-initiated polymerisation of the thiol-ene system has been well investigated. Its applications include adhesives, coatings and opthalmic lenses. It is unlike the usual UV curable polymeric systems which are predominantly based on acrylates. Typically, acrylate systems are not strictly stoichiometric reactions. The thiol-ene process is a reactive composition based on the stoichiometric reaction of olefins (enes, acrylates) and thiols (mercaptans), which polymerise on exposure to UV light. A unique feature of the thiol-ene system is that the reaction is not inhibited by dissolved or ambient oxygen within the system, thereby eliminating the termination reaction which occurs in acrylate systems. The mechanism of the thiol-ene reaction is a step growth addition process which propagates by a free radical chain mechanism to yield the anti-Markovnikov product scheme. The majority of thiol-ene systems investigated focus on multifunctional moieties of thiol and olefin to produce highly cross-linked networks. This discussion will focus on kinetic information obtained from a linear system comprised of a disfunctional thiol (1,8-octanedithiol) and styrene initiated by a UV light source

Modular-block complex on preparation and processing of oil slurry, spilled and raw petroleum

International Nuclear Information System (INIS)

Pak, V.V.

1999-01-01

The use of non-serial small petroleum equipment for development of remote and low output petroleum deposit, collection and processing of spilled petroleum is urgent issue. Joint-stock company Montazhengineering developed and mastered production of small modular-block complexes for preparation and processing of petroleum. The complex can include the following modules: preparation of raw petroleum for getting commodity petroleum; petroleum processing installation for getting gas, diesel fuel and black oil; installation for refining of nafta; installation for cleaning petroleum products from mercaptans; installation for getting basic oil; installation for getting bitumen and mastic; installation for processing of spilled petroleum and oil slurry. Each of modules can work separately and in various combinations depending on input and necessary assortment of commodity petroleum. One of urgent ecological problem in Kazakhstan petroleum-processing regions is large number barns with spilled petroleum and oil slurry. Their processing will allow to solve the ecological and economical problems. Processing of spilled petroleum and oil slurry in developed installations it's possible to get commodity petroleum and petroleum products

[Analysis of volatile sulfur compounds production of oral cavity in preschool children and influencing factors].

Science.gov (United States)

Zhang, Qun; Liu, Xue-nan; Chang, Qing; Ao, Shuang; Zheng, Shu-guo; Xu, Tao

2015-12-18

To investigate the prevalence of volatile sulfur compounds(VSC) in oral cavity of preschool children, and to analyze related factors, thus to provide scientific basis for the prediction and treatment of halitosis. The VSC content (hydrogen sulfide, methyl mercaptan, dimethyl sulfide) of 170 preschool children (4 to 6 years old) was detected by a portable gas chromatograph OralChromaTM. The status of the oral health was evaluated. The living habits and other aspects were obtained through questionnaires from the children's parents. A soft package for social statistics version 13.0 (SPSS 13.0) was used in which univariate analysis and multivariate analysis were utilized to analyze the related factors of halitosis in children. In the study, 34.4% of the total subjects had excessive VSC. Hydrogen sulfide (H₂S) [(1.59 ± 2.41) ng/10 mL] and total VSC concentration [(2.14 ± 4.42) ng/10 mL] in the girls were significantly higher (P<0.05) than those in the boys. The tongue coating score had a significant positive correlation with H2S [tongue coating area (1.68 ± 2.48) ng/10 mL,tongue coating thickness (2.18 ± 2.69) ng/10 mL] and total VSC concentration [tongue coating area, (2.26 ± 4.31) ng/10 mL,tongue coating thickness (2.41 ± 3.02) ng/10 mL , P<0.01]. The site number of DI-S ≥ 2 had a significant positive correlation with methyl mercaptan (CH3SH) and dimethyl sulfide [(CH3)2S] concentration (P<0.01). The concentration of H₂S [(1.19 ± 1.62) ng/10 mL] in children, whose mother had a higher degree of education, was statistically lower (P<0.01). The children who took dessert or sweat drinks more frequently had lower H2S [(1.04 ± 1.55) ng/10 mL, P<0.05] concentration, while CH3SH and (CH3₂)S concentration [(0.29 ± 1.92) ng/10 mL, (0.37 ± 2.06) ng/10 mL, P<0.05) were higher in the children with mouth-breath habit. A high prevalence of halitosis was noted in preschool children. Gender, tongue coating index, debris index-simplified, status of the mother

Physico-chemical studies of effluents and emission of ghee/edible oil industries in Pakistan

International Nuclear Information System (INIS)

Ahmed, I.; Ali, S.; Jan, M.R.

1999-01-01

Samples of the effluents from various Ghee/Edible Oil Industries were collected on fortnightly basis from July 1993 to June 1994 and the emissions from January to April 1994. Parameters such as temperature, pH, conductivity, total dissolved solids (TDS), total suspended solids (TSS), total alkalinity total acidity, total hardness, chemical oxygen demand (COD). chlorides, sulphates, phosphates, silica, calcium magnesium, sodium, and iron were determined in the effluents, Trace metals like copper, manganese, nickel, and zinc were determined by atomic absorption spectroscopy, whereas SO/sub 2/, CO CO/sub 2/, hydrocarbons, hydrogen, nitrogen, oxygen and argon were examined in the flue gases by Gas Chromatography and other standard techniques such as Orsat Gas Analyzer and Dragger Detection Tubes. Remedial measures were suggested for the pollutants exceeding the National Environmental Quality Standards, (NEQS). Parameters like chlorine, ammonia, sulphides, arsenic, cadmium, chromium, cobalt, lead and tin were also analyzed in the effluents and were found to be nil or below the detection limit, while particulate matters, HCl, chlorine, HF, H/sub 2/S, mercaptans and NH/sub 3/ were found to be nil in the flue gases. (author)

Influence of heavy crude oil refining about the mains characteristics of jet fuel; Influencia do refino de petroleos pesados sobre as principais caracteristicas do combustivel de aviacao

Energy Technology Data Exchange (ETDEWEB)

Om, Neyda [Universidade Federal do Rio de Janeiro (UFRJ), RJ (Brazil). Escola de Quimica; Cavado, Alberto; Reyes, Yordanka [Centro de Pesquisas do Petroleo, Cidade de Havana (Cuba); Salazar, Rodolfo [Centro de Eletromagnetismo Aplicado, Cidade de Havana (Cuba); Dominguez, Zulema [Universidade Federal do Rio de Janeiro (UFRJ), RJ (Brazil). Coordenacao dos Programas de Pos-graduacao de Engenharia (COPPE)

2004-07-01

The aviation technology in the world, is to use gas turbines engines feted for fuel type Jet A1. The main exigency of quality for this products is concentrated in extreme security and secure answer during the functioning. The conductivity and thermal stability to oxidation are the principals characteristics to assure these quality exigencies. The use of additives is the methods most used for establish the quality for international specification. The incorporation of heavy crude oils in mixtures to produce fuels has caused a diminution of the quality of the derivatives produced. High viscosity, density and high sulfur content in the heavy crude oils affect some of properties of the jet fuel, influencing in its composition, increasing the mercaptanes and total sulfur content, getting a jet fuel unstable, with low conductivity and highly corrosive. So, for obtain the quality required internationally is necessary use additives. This paper study how the heavy crude oils affect the conductivity and the thermal stability of the jets fuels type Jet A1. Also analyze of the use of dissipater electrostatic and antioxidants additives, to improve these properties in the jet fuel. (author)

A Systematic Study on the Effect of Desilication of Clinoptilolite Zeolite on its Deep-Desulfurization Characteristics

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Rahman Mahmoudi

2016-07-01

Full Text Available Natural clinoptilolite zeolite (CLP in its original or metal ion- exchanged form (Ni2+ is a weak adsorbent for relatively large thiophene derivative molecules like benzothiophene (BT and di-benzothiophene (DBT, due to its rather restricted micro-channel structure. A novelty of this work is that upon desilication treatments, it is possible to enhance the adsorption behavior of Ni2+-exchanged CLP for such large sulfur- containing molecules. A natural CLP zeolite has been desilicated using NaOH solutions in a concentration range of 0.2-2.0 M. The resulting powders have been subjected to XRF, XRD, FTIR, nitrogen adsorption/desorption, TEM and TGA analyses. The adsorption isotherms for the removal of thiophene (TP, BT, DBT and iso-propyl mercaptan (IPM have been obtained experimentally at 20 °C from simulated liquid fuels using iso-octane as solvent. The sample treated with 1.5 M NaOH solution showed the most significant enhancement in adsorptive properties. The selectivity order is IPM > TP > BT > DBT. Regenerability tests show a quasi constant adsorption capacity after the first cycle. The observed phenomena have been thoroughly discussed based on the physico-chemical analyses of the samples.

Method and apparatus for producing food grade carbon dioxide

International Nuclear Information System (INIS)

Nobles, J.E.; Swenson, L.K.

1984-01-01

A method is disclosed of producing food grade carbon dioxide from an impure carbon dioxide source stream containing contaminants which may include light and heavy hydrocarbons (at least C 1 to C 3 ) and light sulfur compounds such as hydrogen sulfide and carbonyl sulfide as well as heavier sulfur constituents in the nature of mercaptans (RSH) and/or organic mono and disulfides (RSR and RSSR). Nitrogen, water and/or oxygen may also be present in varying amounts in the impure feed stream. The feed gas is first rectified with liquid carbon dioxide condensed from a part of the feed stream to remove heavy hydrocarbons and heavy sulfur compounds, then passed through an absorber to effect removal of the light sulfur compounds, next subjected to an oxidizing atmosphere capable of converting all of the C 2 hydrocarbons and optionally a part of the methane to carbon oxides and water, chilled to condense the water in the remaining gas stream without formation of hydrates, liquefied for ease of handling and storage and finally stripped to remove residual contaminants such as methane, carbon monoxide and nitrogen to produce the final food grade carbon dioxide product

Sumpor u ugljenu (Sulphur in Coal

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Rađenović, A.

2004-12-01

Full Text Available The presence of sulphur in coal possesses important environmetal problems in its usage. The sulphur dioxide (S02 emissions produced during coal combustion account for a significant proportion of the total global output of anthropogenic SO2. The extent of sulphur separation depends on several variables such as the form of sulphur in coal, intimacy of contact between minerals and the products of devolatilization. The total sulphur in coal varies in the range of 0.2 - 11 wt %, although in most cases it is beetwen 1 and 3 wt %. Sulphur occurs in a variety of both inorganic and organic forms. Inorganic sulphur is found mainly as iron pyrite, marcasite, pyrrhotite, sphalerite, galena, chalcopirite and as sulphates (rarely exceeds w = 0,1 %. Organic sulphur is found in aromatic rings and aliphatic functionalities usually as mercaptans, aliphatic and aryl sulfides, disulfides and thiophenes. Organic and pyritic sulphur quantities depend on coal rank. Higher rank coals tend to have a high proportion of labile sulphur. All the organic sulphur is bivalent and it is spread throughout the organic coal matrix. Sulphur occurs in all the macerals and most minerals. Vitrinite contains the major part of organic sulphur and metals. Elemental sulphur is produced during coal weathering. The depolymerization methods as pyrolysis and hydrogenation are very drastic methods wich change the structure of the coal and the sulphur groups. In the case of pyrolysis, high levels of desulphurization, in chars and additional production of liquid hydrocarbon can be achieved. Thiophenes and sulphides were the major sulphur components of tars from coal pyrolysis. Hyrdogen sulphide and the lower mercaptans and sulphides were found in the volatile matters. Hydrogen sulphide and thiophenes are practically the only sulphur products of coal hydrogenation. H2S is produced in char hydrodesulphurization. A number of options are available for reducing sulphur emissions including the

An Internalin A Probe-Based Genosensor for Listeria monocytogenes Detection and Differentiation

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Laura Bifulco

2013-01-01

Full Text Available Internalin A (InlA, a protein required for Listeria monocytogenes virulence, is encoded by the inlA gene, which is only found in pathogenic strains of this genus. One of the best ways to detect and confirm the pathogenicity of the strain is the detection of one of the virulence factors produced by the microorganism. This paper focuses on the design of an electrochemical genosensor used to detect the inlA gene in Listeria strains without labelling the target DNA. The electrochemical sensor was obtained by immobilising an inlA gene probe (single-stranded oligonucleotide on the surfaces of screen-printed gold electrodes (Au-SPEs by means of a mercaptan-activated self-assembled monolayer (SAM. The hybridisation reaction occurring on the electrode surface was electrochemically transduced by differential pulse voltammetry (DPV using methylene blue (MB as an indicator. The covalently immobilised single-stranded DNA was able to selectively hybridise to its complementary DNA sequences in solution to form double-stranded DNA on the gold surface. A significant decrease of the peak current of the voltammogram (DPV upon hybridisation of immobilised ssDNA was recorded. Whole DNA samples of L. monocytogenes strains could be discriminated from other nonpathogenic Listeria species DNA with the inlA gene DNA probe genosensor.

Emissions of sulfur gases from marine and freshwater wetlands of the Florida Everglades: Rates and extrapolation using remote sensing

Science.gov (United States)

Hines, Mark E.; Pelletier, Ramona E.; Crill, Patrick M.

1992-01-01

Rates of emissions of the biogenic sulfur (S) gases carbonyl sulfide (COS), methyl mercaptan (MSH), dimethyl sulfide (DMS), and carbon disulfide (CS2) were measured in a variety of marine and freshwater wetland habitats in the Florida Everglades during a short duration period in October using dynamic chambers, cryotrapping techniques, and gas chromatography. The most rapid emissions of greater than 500 nmol/m(sup -2)h(sup -1) occurred in red mangrove-dominated sites that were adjacent to open seawater and contained numerous crab burrows. Poorly drained red mangrove sites exhibited lower fluxes of approximately 60 nmol/m(sup -2)h(sup -1) which were similar to fluxes from the black mangrove areas which dominated the marine-influenced wetland sites in the Everglades. DMS was the dominant organo-S gas emitted especially in the freshwater areas. Spectral data from a scene from the Landsat thematic mapper were used to map habitats in the Everglades. Six vegetation categories were delineated using geographical information system software and S gas emission were extrapolated for the entire Everglades National Park. The black mangrove-dominated areas accounted for the largest portion of S gas emissions to the area. The large area extent of the saw grass communities (42 percent) accounted for approximately 24 percent of the total S emissions.

Treatment Efficiency by means of a Nonthermal Plasma Combined with Heterogeneous Catalysis of Odoriferous Volatile Organic Compounds Emissions from the Thermal Drying of Landfill Leachates

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Daniel Almarcha

2014-01-01

Full Text Available The objective of the present work was to assess the odoriferous volatile organic compounds depuration efficiency of an experimental nonthermal plasma coupled to a catalytic system used for odor abatement of real emissions from a leachate thermal drying plant installed in an urban solid waste landfill. VOC screening was performed by means of HRGC-MS analysis of samples taken at the inlet and at the outlet of the nonthermal plasma system. Odor concentration by means of dynamic olfactometry, total organic carbon, mercaptans, NH3, and H2S were also determined in order to assess the performance of the system throughout several days. Three plasma frequencies (100, 150, and 200 Hz and two catalyst temperatures (150°C and 50°C were also tested. Under conditions of maximum capacity of the treatment system, the results show VOC depuration efficiencies around 69%, with average depuration efficiencies between 44 and 95% depending on the chemical family of the substance. Compounds belonging to the following families have been detected in the samples: organic acids, alcohols, ketones, aldehydes, pyrazines, and reduced sulphur compounds, among others. Average total organic carbon removal efficiency was 88%, while NH3 and H2S removal efficiencies were 88% and 87%, respectively, and odor concentration abatement was 78%.

Parametric and comparative study of the impact of waste pollutants in groundwater: the case of the district of Abidjan (Côte d'Ivoire) and polluted site in Switzerland

Science.gov (United States)

Agnès Kouamé, Amenan; Jaboyedoff, Michel; Derron, Marc-Henri

2013-04-01

Groundwater as natural resources is one of the main sources of water for agricultural, industrial and domestic in developed or developing countries. However this resource, which was considered of good quality, is now threatened by various sources of contamination by human activities. This is the case of the District of Abidjan which has been the victim of toxic waste in 2006 and of an alpine valley in Western Switzerland. Groundwater from these two sites is located in sandy and unconfined aquifers. In fact, the pollutant transport in porous media is influenced by a variety of physical, chemical or biological, complex and interdependent. In Switzerland, where data are available, we simulated steady-state flow and tetrachloroethene transport with a good result showing the tetrachloroethene plume. While in Abidjan, where the data are insufficient, we developed in steady and transient states, flow and contaminants transport models in order to predict the likely evolution of the contaminants in the basement. Contaminants are composed of a very high contents of hydrogen sulfide, organochlorines, sulfur, mercaptan sulfur, and hydrocarbons such as olefins, Paraffins. We made two parametric and comparative studies. The probability of contamination of groundwater is observed over time, taking into account the input parameters of the model and some assumptions.

A new portable sulfide monitor with a zinc-oxide semiconductor sensor for daily use and field study.

Science.gov (United States)

Tanda, Naoko; Washio, Jumpei; Ikawa, Kyoko; Suzuki, Kengo; Koseki, Takeyoshi; Iwakura, Masaki

2007-07-01

For measuring oral malodor in daily clinical practice and in field study, we developed and evaluated a highly sensitive portable monitor system. We examined sensitivity and specificity of the sensor for volatile sulfur compounds (VSC) and obstructive gases, such as ethanol, acetone, and acetaldehyde. Each mouth air provided by 46 people was measured by this monitor, gas chromatography (GC), and olfactory panel and compared with each other. Based on the result, we used the monitor for mass health examination of a rural town with standardized measuring. The sensor detected hydrogen sulfide, methyl mercaptan, and dimethyl sulfide with 10-1000 times higher sensitivity than the other gases. The monitor's specificity was significantly improved by a VSC-selective filter. There were significant correlations between VSC concentration by the sulfide monitor and by GC, and by organoleptic score. Thirty-six percent of 969 examinees had oral malodor in a rural town. Seventy-eight percent of 969 examinees were motivated to take care of their oral condition by oral malodor measuring with the monitor. The portable sulfide monitor was useful to promote oral health care not only in clinics, but also in field study. The simple and quick operation system and the standardized measuring make it one of parameters of oral condition.

Comparative Study on the Characteristics of Weissella cibaria CMU and Probiotic Strains for Oral Care

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Hye-Jin Jang

2016-12-01

Full Text Available Probiotics have been demonstrated as a new paradigm to substitute antibiotic treatment for dental caries, gingivitis, and chronic periodontitis. The present work was conducted to compare the characteristics of oral care probiotics: Weissella cibaria CMU (Chonnam Medical University and four commercial probiotic strains. Survival rates under poor oral conditions, acid production, hydrogen peroxide production, as well as inhibition of biofilm formation, coaggregation, antibacterial activity, and inhibition of volatile sulfur compounds were evaluated. The viability of W. cibaria CMU was not affected by treatment of 100 mg/L lysozyme for 90 min and 1 mM hydrogen peroxide for 6 h. Interestingly, W. cibaria produced less acid and more hydrogen peroxide than the other four probiotics. W. cibaria inhibited biofilm formation by Streptococcus mutans at lower concentrations (S. mutans/CMU = 8 and efficiently coaggregated with Fusobacterium nucleatum. W. cibaria CMU and two commercial probiotics, including Lactobacillus salivarius and Lactobacillus reuteri, showed high antibacterial activities (>97% against cariogens (S. mutans and Streptococcus sobrinus, and against periodontopathogens (F. nucleatum and Porphyromonas gingivalis. All of the lactic acid bacterial strains in this study significantly reduced levels of hydrogen sulfide and methyl mercaptan produced by F. nucleatum and P. gingivalis (p < 0.05. These results suggest that W. cibaria CMU is applicable as an oral care probiotic.

Removal of sulphur-containing odorants from fuel gases for fuel cell-based combined heat and power applications

Energy Technology Data Exchange (ETDEWEB)

De Wild, P.J.; Nyqvist, R.G.; De Bruijn, F.A.; Stobbe, E.R. [ECN Hydrogen and Clean Fossil Fuels, Petten (Netherlands)

2006-02-15

Natural gas (NG) and liquefied petroleum gas (LPG) are important potential feedstocks for the production of hydrogen for fuel cell-based (e.g. proton exchange membrane fuel cells (PEMFC)) or solid oxide fuel Cells (SOFC) combined heat and power (CHP) applications. To prevent detrimental effects on the (electro)catalysts in fuel cell-based combined heat and power installations (FC-CHP), sulphur removal from the feedstock is mandatory. An experimental bench-marking study of adsorbents has identified several candidates for the removal of sulphur containing odorants at low temperature. Among these adsorbents a new material has been discovered that offers an economically attractive means to remove TetraHydroThiophene (THT), the main European odorant, from natural gas at ambient temperature. The material is environmentally benign, easy to use and possesses good activity (residual sulphur levels below 20 ppbv) and capacity for the common odorant THT in natural gas. When compared to state-of-the-art metal-promoted active carbon the new material has a THT uptake capacity that is up to 10 times larger, depending on temperature and pressure. Promoted versions of the new material have shown potential for the removal of THT at higher temperatures and/or for the removal of other odorants such as mercaptans from natural gas or from LPG.

Removal of sulphur-containing odorants from fuel gases for fuel cell-based combined heat and power applications

Energy Technology Data Exchange (ETDEWEB)

de Wild, P.J.; Nyqvist, R.G.; de Bruijn, F.A.; Stobbe, E.R. [Energy Research Centre of The Netherlands ECN, P.O. Box 1, 1755 ZG Petten (Netherlands)

2006-09-22

Natural gas (NG) and liquefied petroleum gas (LPG) are important potential feedstocks for the production of hydrogen for fuel cell-based (e.g. proton exchange membrane fuel cells (PEMFC) or solid oxide fuel Cells (SOFC) combined heat and power (CHP) applications. To prevent detrimental effects on the (electro)catalysts in fuel cell-based combined heat and power installations (FC-CHP), sulphur removal from the feedstock is mandatory. An experimental bench-marking study of adsorbents has identified several candidates for the removal of sulphur containing odorants at low temperature. Among these adsorbents a new material has been discovered that offers an economically attractive means to remove TetraHydroThiophene (THT), the main European odorant, from natural gas at ambient temperature. The material is environmentally benign, easy to use and possesses good activity (residual sulphur levels below 20ppbv) and capacity for the common odorant THT in natural gas. When compared to state-of-the-art metal-promoted active carbon the new material has a THT uptake capacity that is up to 10 times larger, depending on temperature and pressure. Promoted versions of the new material have shown potential for the removal of THT at higher temperatures and/or for the removal of other odorants such as mercaptans from natural gas or from LPG. (author)

Measurement of gas/water uptake coefficients for trace gases active in the marine environment. [Annual report

Energy Technology Data Exchange (ETDEWEB)

Davidovits, P. [Boston Coll., Chestnut Hill, MA (United States). Dept. of Chemistry; Worsnop, D.W.; Zahniser, M.S.; Kolb, C.E. [Aerodyne Research, Inc., Billerica, MA (United States). Center for Chemical and Environmental Physics

1992-02-01

Ocean produced reduced sulfur compounds including dimethylsulfide (DMS), hydrogen sulfide (H{sub 2}S), carbon disulfide (CS{sub 2}), methyl mercaptan (CH{sub 3}CH) and carbonyl sulfide (OCS) deliver a sulfur burden to the atmosphere which is roughly equal to sulfur oxides produced by fossil fuel combustion. These species and their oxidation products dimethyl sulfoxide (DMSO), dimethyl sulfone (DMSO{sub 2}) and methane sulfonic acid (MSA) dominate aerosol and CCN production in clean marine air. Furthermore, oxidation of reduced sulfur species will be strongly influenced by NO{sub x}/O{sub 3} chemistry in marine atmospheres. The multiphase chemical processes for these species must be understood in order to study the evolving role of combustion produced sulfur oxides over the oceans. We have measured the chemical and physical parameters affecting the uptake of reduced sulfur compounds, their oxidation products, ozone, and nitrogen oxides by the ocean`s surface, and marine clouds, fogs, and aerosols. These parameters include: gas/surface mass accommodation coefficients; physical and chemically modified (effective) Henry`s law constants; and surface and liquid phase reaction constants. These parameters are critical to understanding both the interaction of gaseous trace species with cloud and fog droplets and the deposition of trace gaseous species to dew covered, fresh water and marine surfaces.

Measurement of gas/water uptake coefficients for trace gases active in the marine environment

Energy Technology Data Exchange (ETDEWEB)

Davidovits, P. (Boston Coll., Chestnut Hill, MA (United States). Dept. of Chemistry); Worsnop, D.W.; Zahniser, M.S.; Kolb, C.E. (Aerodyne Research, Inc., Billerica, MA (United States). Center for Chemical and Environmental Physics)

1992-02-01

Ocean produced reduced sulfur compounds including dimethylsulfide (DMS), hydrogen sulfide (H{sub 2}S), carbon disulfide (CS{sub 2}), methyl mercaptan (CH{sub 3}CH) and carbonyl sulfide (OCS) deliver a sulfur burden to the atmosphere which is roughly equal to sulfur oxides produced by fossil fuel combustion. These species and their oxidation products dimethyl sulfoxide (DMSO), dimethyl sulfone (DMSO{sub 2}) and methane sulfonic acid (MSA) dominate aerosol and CCN production in clean marine air. Furthermore, oxidation of reduced sulfur species will be strongly influenced by NO{sub x}/O{sub 3} chemistry in marine atmospheres. The multiphase chemical processes for these species must be understood in order to study the evolving role of combustion produced sulfur oxides over the oceans. We have measured the chemical and physical parameters affecting the uptake of reduced sulfur compounds, their oxidation products, ozone, and nitrogen oxides by the ocean's surface, and marine clouds, fogs, and aerosols. These parameters include: gas/surface mass accommodation coefficients; physical and chemically modified (effective) Henry's law constants; and surface and liquid phase reaction constants. These parameters are critical to understanding both the interaction of gaseous trace species with cloud and fog droplets and the deposition of trace gaseous species to dew covered, fresh water and marine surfaces.

Processing and performance of self-healing materials

International Nuclear Information System (INIS)

Tan, P S; Bhattacharyya, D; Zhang, M Q

2009-01-01

Two self-healing methods were implemented into composite materials with self-healing capabilities, using hollow glass fibres (HGF) and microencapsulated epoxy resin with mercaptan as the hardener. For the HGF approach, two perpendicular layers of HGF were put into an E-glass/epoxy composite, and were filled with coloured epoxy resin and hardener. The HGF samples had a novel ball indentation test method done on them. The samples were analysed using micro-CT scanning, confocal microscopy and penetrant dye. Micro-CT and confocal microscopy produced limited success, but their viability was established. Penetrant dye images showed resin obstructing flow of dye through damage regions, suggesting infiltration of resin into cracks. Three-point bend tests showed that overall performance could be affected by the flaws arising from embedding HGF in the material. For the microcapsule approach, samples were prepared for novel double-torsion tests used to generate large cracks. The samples were compared with pure resin samples by analysing them using photoelastic imaging and scanning electron microscope (SEM) on crack surfaces. Photoelastic imaging established the consolidation of cracks while SEM showed a wide spread of microcapsules with their distribution being affected by gravity. Further double-torsion testing showed that healing recovered approximately 24% of material strength.

Catalytic Activity Studies of Vanadia/Silica–Titania Catalysts in SVOC Partial Oxidation to Formaldehyde: Focus on the Catalyst Composition

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Niina Koivikko

2018-02-01

Full Text Available In this work, silica–titania supported catalysts were prepared by a sol–gel method with various compositions. Vanadia was impregnated on SiO2-TiO2 with different loadings, and materials were investigated in the partial oxidation of methanol and methyl mercaptan to formaldehyde. The materials were characterized by using N2 physisorption, X-ray diffraction (XRD, X-ray fluorescence spectroscopy (XRF, X-ray photoelectron spectroscopy (XPS, Scanning transmission electron microscope (STEM, NH3-TPD, and Raman techniques. The activity results show the high importance of an optimized SiO2-TiO2 ratio to reach a high reactant conversion and formaldehyde yield. The characteristics of mixed oxides ensure a better dispersion of the active phase on the support and in this way increase the activity of the catalysts. The addition of vanadium pentoxide on the support lowered the optimal temperature of the reaction significantly. Increasing the vanadia loading from 1.5% to 2.5% did not result in higher formaldehyde concentration. Over the 1.5%V2O5/SiO2 + 30%TiO2 catalyst, the optimal selectivity was reached at 415 °C when the maximum formaldehyde concentration was ~1000 ppm.

Prebiotics mitigate in vitro sulfur-containing odour generation in caecal content of pigs

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Yuan Fan Deng

2015-03-01

Full Text Available The objective of this study was to examine the effects and role of prebiotics, such as inulin, fructo-oligosaccharides (FOS and galactooligosaccharides (GAS, to mitigate sulfur-containing odour gases, hydrogen sulfide (H2S and methyl mercaptan (CH3SH using pigs as in vitro study model. Inocula obtained from pigs were incubated at 39°C for 24 h using 550 mg sterilised substrate (caecal contents supplemented with or without 50 mg prebiotics. Production of total gas, H2S and CH3SH were determined. The results showed that total gas production for the caecal content of pigs was 57.3 mL, and that for H2S and CH3SH was 220.2 and 15.2 μL, respectively. The total gas production increased (P<0.05, whereas concentrations of H2S and CH3SH decreased (P<0.05 with supplementation of prebiotics. Among the prebiotics, inulin was the most effective in mitigating H2S and CH3SH productions, reducing the two malodorous gases by 14.7 and 19.8%, respectively. The reduction of the above two sulfur- containing gases was supported by lower sulfate-reducing bacteria population and higher sulfate radical concentrations in the prebiotics, particularly that of inulin supplementation group.

Smell of danger: an analysis of LP-gas odorization

Energy Technology Data Exchange (ETDEWEB)

Cain, W.S.; Turk, A.

1985-03-01

LP-gas derives warning properties from the odorants ethyl mercaptan or thiophane. Laboratory tests have implied that the average person has the ability to smell the odors before leaking LP-gas reaches one-fifth its lower limit of flammability. Generally, however, laboratory tests ignore or discard persons with a poor sense of smell, especially the elderly and persons with certain types of hyposmia. Some persons who apparently can smell the warning agents when directed may otherwise fail to notice or identify them. Elderly men seem particularly vulnerable to instances of incidental anosmia and olfactory agnosia. Psychophysical testing of the warning agents has been rather unsophisticated. There exists neither a standard protocol for testing nor adequate specification of the perceptual properties that might make one warning agent better than another. Without such developments, improvement in warning agents will fail to occur. Possible improvements include increases in concentration, the use of blends to insure more uniform delivery of agent and, to decrease the perceptual vulnerability of relatively insensitive people, use of agents with favorable psychophysical (stimulus-response) functions and use of agents with favorable adaptation characteristics. Even without a change in existing products, it seems advisable to learn more about the vulnerability of LP-gas users and to employ educational means to reduce risks.

Effect of cysteine and cystine addition on sensory profile and potent odorants of extruded potato snacks.

Science.gov (United States)

Majcher, Małgorzata A; Jeleń, Henryk H

2007-07-11

Aromas generated in extruded potato snacks without and with addition of 0.25, 0.5, and 1% (w/w) of flavor precursors, cysteine and cystine, were compared and evaluated by descriptive sensory profiling. The results showed that high addition of cysteine (0.5 and 1%) resulted in the formation of undesirable odor and taste described as mercaptanic/sulfur, onion-like, and bitter; on the contrary, addition of cystine even at high concentration gave product with pleasant odor and taste, slightly changed into breadlike notes. GC/O analysis showed cysteine to be a much more reactive flavor precursor than cystine, stimulating formation of 12 compounds with garlic, sulfury, burnt, pungent/beer, cabbage/mold, meatlike, roasted, and popcorn odor notes. Further analysis performed by the AEDA technique identified 2-methyl-3-furanthiol (FD 2048) as a most potent odorant of extruded potato snacks with 1% addition of cysteine. Other identified compounds with high FD were butanal, 3-methyl-2-butenethiol, 2-methylthiazole, methional, 2-acetyl-1-pyrroline, and 3-hydroxy-4,5-dimethyl-2(5H)-furanone. In the case of cystine addition (1%) the highest FD factors were calculated for butanal, 2-acetyl-1-pyrroline, benzenemethanethiol, methional, phenylacetaldehyde, dimethyltrisulfide, 1-octen-3-ol, 1,5-octadien-3-one, and 2-acetylpyrazine.

Synthesis of Microporous Materials and Their VSC Adsorption Properties

Energy Technology Data Exchange (ETDEWEB)

Yokogawa, Y; Morikawa, H; Sakanishi, M; Utaka, H; Nakamura, A; Kishida, I, E-mail: yokogawa@imat.eng.osaka-cu.ac.jp [Graduate School of Engineering, Osaka City University, 3-3-138, Sugimoto, Sumiyoshi-ku, Osaka, 558-8585 (Japan)

2011-10-29

Oral malodor is caused by volatile sulfur compounds (VSC) such as hydrogen sulfide (H{sub 2}S), methyl mercaptan and dimethyl sulfide produced in mouth. VSC induces permeability of mucous membrane and oral malodor formation. Thus, the adsorbent which highly adsorbs VSC should be useful for health in mouth and may prevent teeth from decaying. The microporous material, hydrotalcite, was synthesized by a wet method, and the H{sub 2}S adsorption was studied. The samples, identified by powder X-ray diffraction method, were put into glass flask filled with H{sub 2}S gas. The initial concentration of H{sub 2}S was 30 ppm. The change in concentrations of H{sub 2}S was measured at rt, and the amount of H{sub 2}S absorbed on the hydrotalcite for 24 h was 300 micro L/g. The samples were taken out from the above glass flask and put into a pyrolysis plant attached to gas chromatography-mass spectrometry to determine the amount of H{sub 2}S desorbed from samples. Only 3% of H{sub 2}S was desorbed when heated at 500 deg. C. H{sub 2}S in water was also found to adsorb into hydrotalcite, which was confirmed by the headspace gas chromatography with flame photometric detector. The hydrotalcite material should be expected to be an adsorbent material, useful for health in mouth.

Water supply and tree growth. Part II. Flooding

Energy Technology Data Exchange (ETDEWEB)

Kozlowski, T.T.

1982-02-01

Continuous or periodic flooding of soil with fresh or salt water is a common occurrence. Although flooding rapidly depletes soil oxygen the problem of poor soil aeration also exists in extensive areas of unflooded, fine-textured soils. Compounds that may be phytotoxic and accumulate in flooded soils include ethanol, acetaldehyde, cyanogenic compounds, sulphides, CO/sub 2/, iron, manganese, ethane, propylene, fatty acids, hydroxy and dicarboxylic acids, unsaturated acids, aldehydes, ketones, mercaptans, and ethylene. Flooding affects seed germination, stomatal aperture, photosynthesis, permeability of roots, mineral relations, and growth and survival of trees. Although growth of most trees is reduced by flooding it is sometimes increased in a few flood-tolerant species. Flood tolerance of trees varies widely with species, age of trees, and periodicity, duration, and season of occurrence of flooding. Standing water is much more harmful than moving water. Physiological dysfunctions associated with flooding are complex and variously involve the influence of oxygen deficiency, excess CO/sub 2/, a variety of toxic compounds, and altered hormone metabolism. Flood tolerance involves both morphological and physiological adaptations. Important morphological adaptations include formation of lenticels and root regeneration. Physiological adaptations may reflect avoidance of accumulation of ethanol as well as capacity to oxidize the rhizosphere and to tolerate high CO/sub 2/ concentrations in the soil. Adaptations to flooding by salt water include mechanisms for both salt tolerance and avoidance.

Development of biotrickling filters to treat sulfur and VOC emissions. Phase II. Quarterly report No. 2, 31 December 1996-31 March 1997

Energy Technology Data Exchange (ETDEWEB)

NONE

1997-05-29

The Phase II project was initiated on September 30, 1996. The goal of this SBIR project is to develop a cost-effective, efficient biological treatment system, a biotrickiing filter, to treat air emissions of significance to the Navy. These emissions include odors from oily bilge holding tanks, and point sources of hazardous air pollutants (HAPs) such as paint spray booths. Biotrickling filters are similar to scrubbers, but rely on microorganisms on the packing surface to remove and degrade the contaminants. Phase I work identified microbial cultures capable of degrading and growing on air pollutants of importance to the Navy. Greater than 98 percent hydrogen sulfide and methyl mercaptan removal efficiencies were demonstrated for odor applications, and 90 percent VOC (toluene, xylene, MEK, and n-butyl acetate) removal efficiencies were demonstrated for paint-spray booth applications. In addition, three different biomass support packing materials were screened. The objectives of Phase II are to: (1) develop a method to control biofilm growth; (2) establish the full-scale system pressure drop characteristics; (3) establish the effective treatment range; (4) perform overall mass balances and confirm transformation to benign products; (5) demonstrate the technology in the field at a Navy site; and (6) prepare a final report detailing the results and conclusions of the Phase II effort, including an economic analysis.

Advanced oxidation processes for treatment of petroleum refinery sour waters; Processos oxidativos avancados para tratamento de aguas acidas de refinaria de petroleo

Energy Technology Data Exchange (ETDEWEB)

Castro, Antonio V.; Coelho, Alessandra D.; Sant' Anna Junior, Geraldo L.; Dezotti, Marcia [Universidade Federal do Rio de Janeiro (UFRJ), RJ (Brazil). Coordenacao dos Programas de Pos-graduacao de Engenharia (COPPE). Programa de Engenharia Quimica

2004-07-01

The characteristics of the waste water generated by the petroleum refineries are related to the type and amount of processed oil, to the nature and the efficiency of the refining operation. The effluents are composed basically of oily waters, originating from of the contact with the oil. Among them, the current of sour water is one of the most preoccupying due to its composition: sulfide, ammonia, mercaptans, phenol, dissolved oil, basic pH, dissolved organic carbon (DOC) and chemical oxygen demand (COD) high. The aim of this work was to evaluate the advanced oxidation processes to degrade sour water (UV radiation, H{sub 2}O{sub 2} and H{sub 2}O{sub 2}/UV, photocatalysis, Fenton and photo-Fenton). All process, except Fenton and photo-Fenton, did not supply satisfactory results, reducing 25% of initial DOC, which it is of 450 mg/L. The results using the Fenton process reached removal of 50% of the initial COD, and when photo- Fenton process obtaining removal of 90%. The processes Fenton and photo-Fenton were shown capable to degrade this kind of waste water, minimizing the environmental problems and corrosion, operating as a pre-treatment for the biological system, or acting alone to degrade the organic matter contained, seeking the water reuse. The effluent used in this work came from Duque de Caxias Refinery (Reduc)/PETROBRAS. (author)

Sulphur chemistry in the L1544 pre-stellar core

Science.gov (United States)

Vastel, Charlotte; Quénard, D.; Le Gal, R.; Wakelam, V.; Andrianasolo, A.; Caselli, P.; Vidal, T.; Ceccarelli, C.; Lefloch, B.; Bachiller, R.

2018-05-01

The L1544 pre-stellar core has been observed as part of the ASAI IRAM 30m Large Program as well as follow-up programs. These observations have revealed the chemical richness of the earliest phases of low-mass star-forming regions. In this paper we focus on the twenty-one sulphur bearing species (ions, isotopomers and deuteration) that have been detected in this spectral-survey through fifty one transitions: CS, CCS, C3S, SO, SO2, H2CS, OCS, HSCN, NS, HCS+, NS+ and H2S. We also report the tentative detection (4 σ level) for methyl mercaptan (CH3SH). LTE and non-LTE radiative transfer modelling have been performed and we used the NAUTILUS chemical code updated with the most recent chemical network for sulphur to explain our observations. From the chemical modelling we expect a strong radial variation for the abundances of these species, which mostly are emitted in the external layer where non thermal desorption of other species has previously been observed. We show that the chemical study cannot be compared to what has been done for the TMC-1 dark cloud, where the abundance is supposed constant along the line of sight, and conclude that a strong sulphur depletion is necessary to fully reproduce our observations of the prototypical pre-stellar core L1544.

Preparation of nanoencapsulated phase change material as latent functionally thermal fluid

Energy Technology Data Exchange (ETDEWEB)

Fang Yutang; Kuang Shengyan; Gao Xuenong; Zhang Zhengguo, E-mail: ppytfang@scut.edu.c [Key Laboratory of Enhanced Heat Transfer and Energy Conservation, Ministry of Education, South China University of Technology, Guangzhou 510640 (China)

2009-02-07

Nanoencapsulated phase change material with polystyrene as the shell and n-octadecane as the core was synthesized using the ultrasonic technique and miniemulsion in situ polymerization. The influences of polymerization factors, including initiator, chain transfer agent (CTA), surfactant, n-octadecane/styrene ratio and hydrophilic co-monomer, on the morphology and thermophysical properties of nanocapsules were systematically investigated. The optimized polymerization conditions were 0.5 wt% of initiator (2,2-azobisisobutyronitrile), 0.4 wt% of CTA (n-dodecyl mercaptan), 2% of composite surfactants which were composed of sodium dodecyl sulfate and poly-(ethylene glycol) monooctylphenyl ether by 1 : 1 in weight ratio, 1 wt% of hydrophilic co-monomer butyl acrylate or 3 wt% of methyl methacrylate and 1 : 1 n-octadecane to styrene in weight ratio. Under these conditions, the z-average size of prepared nanocapsules was 124 nm and the phase change enthalpy was 124.4 kJ kg{sup -1}. The heat capacity was as high as 11.61 kJ kg{sup -1} K{sup -1} at the latex concentration of 20.6 wt%. Thermal stability and viscosity testing show that this fluid had excellent resistance to thermal shock (after 100 cycles, no liquid Oct was observed during heating) and low viscosity (only 3.61 mPa s at the latex concentration of 20.6 wt%), which seems to be promising as a latent functionally thermal fluid.

Relationship of a turbidity of an oral rinse with oral health and malodor in Vietnamese patients.

Science.gov (United States)

Pham, Thuy A V

2014-05-01

In the present study, the relationship between the turbidity of mouth-rinse water and oral health conditions, including oral malodor, in patients with (n = 148) and without (n = 231) periodontitis was examined. The turbidity of 20 mL distilled water that the patients rinsed in their mouths 10 times was measured using a turbidimeter. Oral malodor was evaluated using an organoleptic test and Oral Chroma. Oral health conditions, including decayed teeth, periodontal status, oral hygiene status, proteolytic activity of the N-benzoyl-dl-arginine-2-napthilamide (BANA) test on the tongue coating, and salivary flow rate, were assessed. Turbidity showed significant correlations with oral malodor and all oral health parameters in the periodontitis group. In the non-periodontitis group, turbidity showed significant correlations with oral malodor and oral health parameters, including dental plaque, tongue coating, BANA test, and salivary flow rate. The regression analysis indicated that turbidity was significantly associated with methyl mercaptan and the BANA test in the periodontitis group, and with hydrogen sulfide, dental plaque, tongue coating, and salivary flow rate in the non-periodontitis group. The findings of the present study indicate that the turbidity of mouth-rinse water could be used as an indicator of oral health conditions, including oral malodor. © 2013 Wiley Publishing Asia Pty Ltd.

A randomized, double-blind, crossover, placebo-controlled clinical trial to assess effects of the single ingestion of a tablet containing lactoferrin, lactoperoxidase, and glucose oxidase on oral malodor.

Science.gov (United States)

Nakano, Manabu; Shimizu, Eiju; Wakabayashi, Hiroyuki; Yamauchi, Koji; Abe, Fumiaki

2016-03-22

The main components of oral malodor have been identified as volatile sulfur compounds (VSCs) including hydrogen sulfide (H2S) and methyl mercaptan (CH3SH). VSCs also play an important role in the progression of periodontal disease. The aim of the present study was to assess the effects of the single ingestion of a tablet containing 20 mg of lactoferrin, 2.6 mg of lactoperoxidase, and 2.6 mg of glucose oxidase on VSCs in the mouth. Subjects with VSCs greater than the olfactory threshold in their mouth air ingested a test or placebo tablet in two crossover phases. The concentrations of VSCs were monitored at baseline and 10 and 30 min after ingestion of the tablets using portable gas chromatography. Thirty-nine subjects were included in the efficacy analysis based on a full analysis set (FAS). The concentrations of total VSCs and H2S at 10 min were significantly lower in the test group than in the placebo group (-0.246 log ng/10 ml [95 % CI -0.395 to -0.098], P = 0.002; -0.349 log ng/10 ml; 95 % CI -0.506 to -0.192; P oxidase has suppressive effects on oral malodor. This trial was registered with the University Hospital Medical Information Network Clinical Trial Registry (number: UMIN000015140 , date of registration: 16/09/2014).

Removal of odor originating from kitchen wastewater treatment facilities by activated carbon impregnated iodic acid; Chubo haisui shori shisetsu kara hasseisuru akushu no yososan tenchaku kasseitan ni yoru jokyo

Energy Technology Data Exchange (ETDEWEB)

Yano, H.; Hashimoto, S.; Yonemura, S. [Shimizu Corp., Tokyo (Japan); Shoda, M. [Research Laboratory of Resources Utilization, Yokohama (Japan)

1997-07-10

Activated carbon impregnated iodic acid (deodorant D) was developed as a new deodorant. Deodorization performance of deodorant D as well as three kinds of commercial activated carbons (deodorant A, B and C) was tested for odors originating from the kitchen wastewater treatment facilities of one commercial building. The odor exhausted from this facility was medium concentration between 422 and 31,620. The main odorous compounds were hydrogen sulfide (0.076 to 15.7 ppm) and methyl mercaptan (not detected to 0.081 ppm). The hydrogen sulfide contribution to the odor concentration was about 90%. The main apparatuses from which the odors were originating were the raw water tank and the pressurized flotation tank. The total odor emission rate was between 10{sup 4.9} and 10{sup 5.7} Nm{sup 3}/min. For the performance test for deodorants, fixed bed adsorption experimental equipment was used, and the breakthrough time of odor concentration and hydrogen sulfide were used as indexes. Correlation between the contact time and the breakthrough time was observed for all of the deodorants. For a contact time of 0.5 sec, the breakthrough times for odor concentration were D>C>B>A, and the breakthrough times for hydrogen sulfide were D>C>B>A. Effectiveness of activated carbon impregnated iodic acid was recognized. 11 refs., 7 figs., 7 tabs.

Problems in instrumentation for S-odorant emissions

International Nuclear Information System (INIS)

Hall, H.J.

1974-01-01

Instrumentation to measure sulfur-containing odorants in stack emissions is much more difficult than in the ambient atmosphere, and must be matched to the specific source: key components aside from H 2 S are methyl mercaptan in paper mills, COS/CS 2 in a refinery Claus plant, and SO 2 /SO 3 in a combustion stack. Satisfactory operation for a period of six months was not achieved by any instrument in this service, in a lab and field evaluation of eight instruments of three types commercially available as of 1971. The effects of interferent gases H 2 O, SO 2 , CO 2 /CO and particulates which are diluted in ambient samples are greatly aggravated in stack gases, where the ratio of odorant to interferent may be 1:1000 or less, due to the very great sensitivity of human receptors to S-odorants. The most serious problem proved to be the analysis for odorless carbonyl sulfide, which is commonly formed where S compounds are oxidized in a reducing atmosphere. This COS has been undetected or mistaken for odorous H 2 S in most analyses. A field instrument for the general case would provide exactly simultaneous readings at five minute intervals or less for the five components H 2 S, SO 2 , COS, CSH, and total S, or their equivalent. This may be simplified to four components or less only when the composition of the sample gas is positively known

Novel monoclonal autoantibody specificity associated with ribonucleoprotein complexes

International Nuclear Information System (INIS)

Winkler, A.; Watson-McKown, R.; Wise, K.

1986-01-01

The authors describe an IgG/sub 2a/, kappa monoclonal autoantibody (mAb) F78 derived from a 6-month old MRL-Mp lpr/lpr mouse that recognizes a novel epitope associated with small nuclear ribonuclear protein complexes (snRNP). Indirect immunofluorescent staining of HEp-2 cells with F78 showed a nonnucleolar speckled nuclear pattern characteristic of anti-RNP and anti-Sm mAbs which could be abrogated by pretreating fixed cells with 0.1M HCl prior to staining. Immunoblots of whole cell extracts (dissociated in SDS, urea and mercaptan at 4 0 C then subjected to SDS-PAGE) showed that F78 selectively bound to a component of M/sub r/ = 100,000 clearly distinct from components recognized by two mAbs described by Billings et al that detected, respectively, proteins of M/sub r/ = 70,000 associated with RNP and M/sub r/ = 13,000 associated with Sm. Incubation of extracts at 100 0 C prior to SDS-PAGE eliminated subsequent binding of F78 but not of the other nAbs. F78 as well as the other mAbs selectively immunoprecipitated characteristic patterns of small nuclear RNAs (U 1 , U 2 , U 4 , U 5 , U 6 ) from extracts of 32 P-phosphate labeled HeLa cells. These results suggest a new specificity associated with snRNP that is recognized in the MRL autoimmune response

A new ppb-gas analyzer by means of GC-ion mobility spectrometry (GC-IMS)

International Nuclear Information System (INIS)

Leonhardt, J.W.

2003-01-01

IMS-detectors are using beta-sources like tritium or nickel-63. This detection principle uses fast ion-molecular reactions between air cluster ions, produced by beta ionization and the analyte. The system works at normal pressure, the very high sensitivity and selectivity is used widely in industry, research, medicine and environmental control. In the last few years especially, small tritium sources were reduced to a level of some 50 MBq, which is 20 times less than the exemption levels for these sources. One of the handicaps of that technology is the problem of cross sensitivities. To overcome these problems a special GC-column of 1 m length has been included into the gas inlet and mixtures of compounds get separated by their retention times before entering the drift sensor. By means of that method a new analytical quality of IMS is arrived. The application of these analytical devices got a spin off in the last year. The main applications being discussed are as follows: (1) anti terror systems in buildings and facilities, (2) working place monitoring in chemical industry, (3) microelectronics: HF, HCl, Cl 2 , NMP, NH 3 , NO 2 , SO 2 , (4) environment: NH 3 , HCN, HCl, CH 2 O, organic compounds, SO 2 , NO 2 , (5) gas and petrol: gas-carottage, H 2 S, mercaptans, (6) household, furniture: solvents, clue, organic vapour from furniture, and (7) health care: diagnostics of various diseases. (author)

Analysis of Relative Concentration of Ethanol and Other Odorous Compounds (OCs) Emitted from the Working Surface at a Landfill in China

Science.gov (United States)

Li, Dong; Lu, Wenjing; Liu, Yanjun; Guo, Hanwen; Xu, Sai; Ming, Zhongyuan; Wang, Hongtao

2015-01-01

Estimating odor emissions from landfill sites is a complicated task because of the various chemical and biological species that exist in landfill gases. In this study, the relative concentration of ethanol and other odorous compounds emitted from the working surface at a landfill in China was analyzed. Gas sampling was conducted at the landfill on a number of selected days from March 2012 to March 2014, which represented different periods throughout the two years. A total of 41, 59, 66, 54, 63, 54, 41, and 42 species of odorous compounds were identified and quantified in eight sampling activities, respectively; a number of 86 species of odorous compounds were identified and quantified all together in the study. The measured odorous compounds were classified into six different categories (Oxygenated compounds, Halogenated compounds, Terpenes, Sulfur compounds, Aromatics, and Hydrocarbons). The total average concentrations of the oxygenated compounds, sulfur compounds, aromatics, halogenated compounds, hydrocarbons, and terpenes were 2.450 mg/m3, 0.246 mg/m3, 0.203 mg/m3, 0.319 mg/m3, 0.530 mg/m3, and 0.217 mg/m3, respectively. The relative concentrations of 59 odorous compounds with respect to the concentration of ethyl alcohol (1000 ppm) were determined. The dominant contaminants that cause odor pollution around the landfill are ethyl sulfide, methyl mercaptan, acetaldehyde, and hydrogen sulfide; dimethyl disulfide and dimethyl sulfide also contribute to the pollution to a certain degree. PMID:25769100

A five-year history of hazardous materials incidents in Chester County, PA

International Nuclear Information System (INIS)

Shorten, C.V.; McNamara, J.

1993-01-01

The Emergency Planning and Community Right-to-Know Act (EPCRA) of 1986 established Local Emergency Planning Committees (LEPCs) to oversee emergency response planning at the community level. In Pennsylvania, each county was assigned its own LEPC, and Chester County held its first LEPC meeting on October 15, 1987. From the data of that meeting through September 1992, 300 hazardous materials incidents have been reported. The majority of these incidents were met with fire department response, but several warranted response by hazardous materials teams. This report presents an analysis of the database of reported hazardous materials incidents in Chester County, including chemical identification, amount released, type of response, location, and trends. Over 235 of the reported spills were either gasoline, diesel fuel, home heating oil, or kerosene, often in five to 50 gallon amounts from transportation accidents. A number of extremely hazardous substance (EHS) incidents were reported, however, including sulfuric acid, chlorine, ammonia, phosphorus, formaldehyde, bromine, methyl mercaptan, and hydrofluoric acid. The most commonly released EHS's were ammonia and chlorine. The number of hazardous materials incidents reported in Chester County increased from only 14 in 1988 to 95 in 1991, with 67 in 1992 through September. This dramatic increase is attributable to both increased reporting and an increased number of incidents. This database clearly indicates both the success of EPCRA reporting system and the magnitude of hazardous materials incidents in this part of Pennsylvania

Utilização de NBR modificada com grupos 2-oxazolina em misturas de NBR/EVA Utilization of 2-oxazoline modified NBR in NBR/EVA blends

Directory of Open Access Journals (Sweden)

Mauricio S. M. Almeida

2003-06-01

Full Text Available Misturas envolvendo borracha nitrílica e copolímeros de etileno-acetato de vinila na proporção 70:30 % em peso, foram preparadas na presença de borracha nitrílica funcionalizada com 2-oxazolina isoladamente ou combinada com EVA funcionalizado com grupos hidroxila, carboxila ou mercaptana. A reação entre os grupos funcionais foi verificada por análise de FTIR da fração insolúvel de amostras não vulcanizadas e pelo decréscimo nos valores de tan delta nos ensaios dinâmico-mecânicos. A utilização desses copolímeros funcionalizados não influenciou significativamente as propriedades mecânicas, provavelmente devido à proporção da mistura utilizada (rica em NBR o que facilita a localização da NBR funcionalizada no interior da fase elastomérica.Nitrile rubber/ethylene-vinyl acetate copolymer (NBR/EVA blends with ratio of 70/30 wt% were prepared in the presence of functionalized NBR with 2-oxazoline groups. This functionalized copolymer was employed alone or in combination with EVA copolymer functionalized with hydroxyl, carboxyl or mercaptan groups. The reaction between the functional groups was confirmed by FTIR analysis of the unvulcanized samples insoluble fraction, and by the decrease in the tan delta values. The mechanical properties were not substantially affected by the presence of these functionalized copolymers, probably due to the proportion of blend composition (with high amount of NBR, thus forcing the location of functionalized NBR inside the elastomer phase.

Efficacy and role of inulin in mitigation of enteric sulfur-containing odor in pigs.

Science.gov (United States)

Deng, Yuan-Fan; Liu, Yuan-Yuan; Zhang, Yi-Tao; Wang, Yan; Liang, Juan-Boo; Tufarelli, Vincenzo; Laudadio, Vito; Liao, Xin-Di

2017-06-01

The efficacy and role of inulin in the mitigation of enteric sulfur-containing odor gases hydrogen sulfide (H 2 S) and methyl mercaptan (CH 3 SH) in pigs were examined in this study. Twelve Duroc × Landrace × Yorkshire male finisher pigs (60.7 ± 1.9 kg), housed individually in open-circuit respiration chambers, were randomly assigned to two dietary groups, namely basal diet (control) and basal diet supplemented with 1% (w/w) inulin. At the end of the 45 day experiment, pigs were slaughtered and volatile fatty acid (VFA) concentration, sulfate radical (SO 4 2 - ) concentration, population of sulfate-reducing bacteria (SRB) and expression of methionine gamma-lyase (MGL) gene were determined in contents from the caecum, colon (two segments) and rectum. Metabonomic analysis was used to compare differences in biochemical composition, and the Illumina MiSeq procedure to investigate differences in bacterial components, in the different parts of the large intestine between inulin-supplemented and inulin-free (control) groups. Inulin decreased (P inulin treatment, whereas valerate concentration and MGL mRNA expression decreased (P inulin-supplemented pigs, suggesting that inulin mitigates H 2 S generation from the SO 4 2 - reduction pathway by reducing the growth of SRB. The results showed that inulin mitigates CH 3 SH generation via three methionine degradation metabolic pathways and H 2 S generation from two cysteine degradation metabolic pathways, thus resulting in increased synthesis of these two sulfur-containing amino acids in the pig large intestine. © 2016 Society of Chemical Industry. © 2016 Society of Chemical Industry.

Effect of naphtha diluent on greenhouse gases and reduced sulfur compounds emissions from oil sands tailings.

Science.gov (United States)

Gee, Kathleen F; Poon, Ho Yin; Hashisho, Zaher; Ulrich, Ania C

2017-11-15

The long-term storage of oil sands tailings has resulted in the evolution of greenhouse gases (CH 4 and CO 2 ) as a result of residual organics biodegradation. Recent studies have identified black, sulfidic zones below the tailings-water interface, which may be producing toxic sulfur-containing gases. An anaerobic mesocosm study was conducted over an 11-week period to characterize the evolution of CH 4 , CO 2 and reduced sulfur compounds (RSCs) (including H 2 S) in tailings as it relates to naphtha-containing diluent concentrations (0.2, 0.8, and 1.5% w/v) and microbial activity. Our results showed that RSCs were produced first at 0.12μmol°RSCs/mL MFT (1.5% w/v diluent treatment). RSCs contribution (from highest to lowest) was H 2 S and 2-methylthiophene>2.5-dimethylthiophene>3-methylthiophene>thiofuran>butyl mercaptan>carbonyl sulfide, where H 2 S and 2-methylthiophene contributed 81% of the gas produced. CH 4 and CO 2 production occurred after week 5 at 40.7μmolCH 4 /mL MFT and 5.9μmolCO 2 /mL MFT (1.5% w/v diluent treatment). The amount of H 2 S and CH 4 generated is correlated to the amount of diluent present and to microbial activity as shown by corresponding increases in sulfate-reducers' Dissimilatory sulfite reductase (DsrAB) gene and methanogens' methyl-coenzyme M reductase (MCR) gene. Copyright © 2017 Elsevier B.V. All rights reserved.

Dechlorination of chloropicrin and 1,3-dichloropropene by hydrogen sulfide species: redox and nucleophilic substitution reactions.

Science.gov (United States)

Zheng, Wei; Yates, Scott R; Papiernik, Sharon K; Guo, Mingxin; Gan, Jianying

2006-03-22

The chlorinated fumigants chloropicrin (trichloronitromethane) and 1,3-dichloropropene (1,3-D) are extensively used in agricultural production for the control of soilborne pests. The reaction of these two fumigants with hydrogen sulfide species (H2S and HS-) was examined in well-defined anoxic aqueous solutions. Chloropicrin underwent an extremely rapid redox reaction in the hydrogen sulfide solution. Transformation products indicated reductive dechlorination of chloropicrin by hydrogen sulfide species to produce dichloro- and chloronitromethane. The transformation of chloropicrin in hydrogen sulfide solution significantly increased with increasing pH, indicating that H2S is less reactive toward chloropicrin than HS- is. For both 1,3-D isomers, kinetics and transformation products analysis revealed that the reaction between 1,3-D and hydrogen sulfide species is an S(N)2 nucleophilic substitution process, in which the chlorine at C3 of 1,3-D is substituted by the sulfur nucleophile to form corresponding mercaptans. The 50% disappearance time (DT50) of 1,3-D decreased with increasing hydrogen sulfide species concentration at a constant pH. Transformation of 1,3-D was more rapid at high pH, suggesting that the reactivity of hydrogen sulfide species in the experimental system stems primarily from HS-. Because of the relatively low smell threshold values and potential environmental persistence of organic sulfur products yielded by the reaction of 1,3-D and HS-, the effects of reduced sulfide species should be considered in the development of alternative fumigation practices, especially in the integrated application of sulfur-containing fertilizers.

Changes in salivary microbiota increase volatile sulfur compounds production in healthy male subjects with academic-related chronic stress.

Directory of Open Access Journals (Sweden)

Bruno Dias Nani

Full Text Available To investigate the associations among salivary bacteria, oral emanations of volatile sulfur compounds, and academic-related chronic stress in healthy male subjects.Seventy-eight healthy male undergraduate dental students were classified as stressed or not by evaluation of burnout, a syndrome attributed to academic-related chronic stress. This evaluation was carried out using the Maslach Burnout Inventory-Student Survey questionnaire. Oral emanations of hydrogen sulfide, methyl mercaptan, and dimethyl sulfide were measured using an Oral Chroma™ portable gas chromatograph. The amounts in saliva of total bacteria and seven bacteria associated with halitosis were quantified by qPCR. The in vitro production of H2S by S. moorei and/or F. nucleatum was also measured with the Oral Chroma™ instrument.The stressed students group showed increased oral emanations of hydrogen sulfide and dimethyl sulfide, together with higher salivary Solobacterium moorei levels (p < 0.05, Mann Whitney test. There were moderate positive correlations between the following pairs of variables: Fusobacterium nucleatum and S. moorei; F. nucleatum and hydrogen sulfide; Tannerella forsythia and F. nucleatum; T. forsythia and S. moorei. These correlations only occurred for the stressed group (p < 0.05, Spearman correlation. The in vitro experiment demonstrated that S. moorei increased H2S production by F. nucleatum (p < 0.05, ANOVA and Tukey's test.The increased amount of S. moorei in saliva, and its coexistence with F. nucleatum and T. forsythia, seemed to be responsible for increased oral hydrogen sulfide in the healthy male stressed subjects.

Effect of garlic oil and four of its compounds on rumen microbial fermentation.

Science.gov (United States)

Busquet, M; Calsamiglia, S; Ferret, A; Carro, M D; Kamel, C

2005-12-01

Different concentrations (3, 30, 300, and 3000 mg/L of culture fluid) of garlic oil (GAR), diallyl sulfide (DAS), diallyl disulfide (DAD), allicin (ALL), and allyl mercaptan (ALM) were incubated for 24 h in diluted ruminal fluid with a 50:50 forage:concentrate diet (17.7% crude protein; 30.7% neutral detergent fiber) to evaluate their effects on rumen microbial fermentation. Garlic oil (30 and 300 mg/L), DAD (30 and 300 mg/L), and ALM (300 mg/L) resulted in lower molar proportion of acetate and higher proportions of propionate and butyrate. In contrast, at 300 mg/L, DAS only increased the proportion of butyrate, and ALL had no effects on volatile fatty acid proportions. In a dual-flow continuous culture of rumen fluid fed the same 50:50 forage:concentrate diet, addition of GAR (312 mg/L), DAD (31.2 and 312 mg/L), and ALM (31.2 and 312 mg/L) resulted in similar changes to those observed in batch culture, with the exception of the lack of effect of DAD on the proportion of propionate. In a third in vitro study, the potential of GAR (300 mg/L), DAD (300 mg/L), and ALM (300 mg/L) to decrease methane production was evaluated. Treatments GAR, DAD, and ALM resulted in a decrease in methane production of 73.6, 68.5, and 19.5%, respectively, compared with the control. These results confirm the ability of GAR, DAD, and ALM to decrease methane production, which may help to improve the efficiency of energy use in the rumen.

Thermoneutral isotope exchange reactions of cations in the gas phase

International Nuclear Information System (INIS)

Ausloos, P.; Lias, S.G.

1981-01-01

Rate constants have been measured for reactions of the type AD 2 + + MH → MD + ADH + , where AD 2 + is CD 3 CND + , CD 3 CDOD + , (CD 3 COCD 3 )D + , or (C 2 D 5 ) 2 OD + and the MH molecules are alcohols, acids, mercaptans, H 2 S, AsH 3 , PH 3 , or aromatic molecules. Rate constants are also presented for the reactions Ar/sub H/D + + D 2 O → Ar/sub d/D + + HDO, where Ar/sub H/D + is a deuteronated aromatic molecule and Ar/sub D/D + is the same species with a D atom incorporated on the ring. In all but two cases, the competing deuteron transfer is sufficiently endothermic that it cannot be observed under the conditions of the ICR experiments at 320 to 420 K. The efficiencies of the isotope exchange reactions are interpreted in terms of estimated potential surface cross sections for the reactions AD 2 + + MH → [AD 2 + MH] → [ADMHD + ] → [ADH + MD] → ADH + + MD. When the formation of the [ADMHD + ] complex is estimated to be thermoneutral or slightly endothermic, the isotope exchange process is inefficient (probability of a reactive collision 2 + MH] → [ADMHD + ] is exothermic. For most of the systems, trends in reaction efficiency appear to be related to factors such as dipole moments of reactant species (or for aromatic compounds, the electron-donating or -withdrawing properties of ring substituents) which influence the relative orientation of the two reactant species in the complex

Characterization of industrial waste from a natural gas distribution company and management strategies: a case study of the East Azerbaijan Gas Company (Iran).

Science.gov (United States)

Taghipour, Hassan; Aslhashemi, Ahmad; Assadi, Mohammad; Khodaei, Firoz; Mardangahi, Baharak; Mosaferi, Mohammad; Roshani, Babak

2012-10-01

Although a fundamental prerequisite for the successful implementation of any waste management plan is the availability of sufficient and accurate data, there are few available studies regarding the characterization and management of gas distribution company waste (GDCW). This study aimed to characterize the industrial waste generated by the East Azerbaijan Gas Distribution Company (EAGDC) and to present environmental management strategies. The EAGDC serves 57 cities and 821 villages with a total population of more than 2.5 million as well as numerous industrial units. The methodology of this study was based on a checklist of data collected from each zone of the company, site visits (observation), and quantity and quality analysis according to the formal data available from different zones. The results indicate that more than 35 different kinds of industrial solid waste are generated in different industrial installations. The most important types of generated waste include empty barrels (including mercaptans, diesel fuel, deionized waters and oil), faulty gas meters and regulators, a variety of industrial oils, sleeves, filter elements and faulty pipes, valves and fittings. The results indicated that, currently, GDCW is generally handled and disposed of with domestic waste, deposited in companies' installation yards and stores or, sometimes, recycled through non-scientific approaches that can create health risks to the public and the environment, even though most of the GDCW was determined to be recyclable or reusable materials. This study concludes that gas distribution companies must pay more attention to source reduction, recycling and reusing of waste to preserve natural resources, landfill space and the environment.

Short-term gas dispersion in idealised urban canopy in street parallel with flow direction

Science.gov (United States)

Chaloupecká, Hana; Jaňour, Zbyněk; Nosek, Štěpán

2016-03-01

Chemical attacks (e.g. Syria 2014-15 chlorine, 2013 sarine or Iraq 2006-7 chlorine) as well as chemical plant disasters (e.g. Spain 2015 nitric oxide, ferric chloride; Texas 2014 methyl mercaptan) threaten mankind. In these crisis situations, gas clouds are released. Dispersion of gas clouds is the issue of interest investigated in this paper. The paper describes wind tunnel experiments of dispersion from ground level point gas source. The source is situated in a model of an idealised urban canopy. The short duration releases of passive contaminant ethane are created by an electromagnetic valve. The gas cloud concentrations are measured in individual places at the height of the human breathing zone within a street parallel with flow direction by Fast-response Ionisation Detector. The simulations of the gas release for each measurement position are repeated many times under the same experimental set up to obtain representative datasets. These datasets are analysed to compute puff characteristics (arrival, leaving time and duration). The results indicate that the mean value of the dimensionless arrival time can be described as a growing linear function of the dimensionless coordinate in the street parallel with flow direction where the gas source is situated. The same might be stated about the dimensionless leaving time as well as the dimensionless duration, however these fits are worse. Utilising a linear function, we might also estimate some other statistical characteristics from datasets than the datasets means (medians, trimeans). The datasets of the dimensionless arrival time, the dimensionless leaving time and the dimensionless duration can be fitted by the generalized extreme value distribution (GEV) in all sampling positions except one.

A novel assessment of odor sources using instrumental analysis combined with resident monitoring records for an industrial area in Korea

Science.gov (United States)

Lee, Hyung-Don; Jeon, Soo-Bin; Choi, Won-Joon; Lee, Sang-Sup; Lee, Min-Ho; Oh, Kwang-Joong

2013-08-01

The residents living nearby the Sa-sang industrial area (SSIA) continuously were damaged by odorous pollution since 1990s. We determined the concentrations of reduced sulfur compounds (RSCs) [hydrogen sulfide (H2S), methyl mercaptan (CH3SH), dimethyl sulfide (DMS), and dimethyl disulfide (DMDS)], nitrogenous compounds (NCs) [ammonia (NH3) and trimethylamine (TMA)], and carbonyl compounds (CCs) [acetaldehyde and butyraldehyde] by instrumental analysis in the SSIA in Busan, Korea from Jun to Nov, 2011. We determined odor intensity (OI) based on the concentrations of the odorants and resident monitoring records (RMR). The mean concentration of H2S was 10-times higher than NCs, CCs and the other RSC. The contribution from RSCs to the OI was over 50% at all sites excluding the A-5 (chemical production) site. In particular, A-4 (food production) site showed more than 8-times higher the sum of odor activity value (SOAV) than the other sites. This suggested that the A-4 site was the most malodorous area in the SSIA. From the RMR analysis, the annoyance degree (OI ≥ 2) was 51.9% in the industrial area. The 'Rotten' smell arising from the RSCs showed the highest frequency (25.3%) while 'Burned' and 'Other' were more frequent than 'Rotten' in the residential area. The correlation between odor index calculated by instrumental analysis and OI from the RMR was analyzed. The Pearson correlation coefficient (r) of the SOAV was the highest at 0.720 (P food production causes significant annoyance in the SSIA. We also confirm RMR data can be used effectively to evaluate the characteristic of odorants emitted from the SSIA.

The sulfur dilemma: Are there biosignatures on Europa's icy and patchy surface?

International Nuclear Information System (INIS)

Chela-Flores, J.

2006-12-01

We discuss whether sulphur traces on Jupiter's moon Europa could be of biogenic origin. The compounds detected by the Galileo mission have been conjectured to be endogenic, most likely of cryovolcanic origin, due to their non-uniform distribution in patches. The Galileo space probe first detected the sulphur compounds, as well as revealing that this moon almost certainly has a volcanically heated and potentially habitable ocean hiding beneath a surface layer of ice. In planning future exploration of Europa there are options for sorting out the source of the surficial sulphur. For instance, one possibility is searching for the sulphur source in the context of the study of the Europa Microprobe In Situ Explorer (EMPIE), which has been framed within the Jovian Minisat Explorer Technology Reference Study (ESA). It is conceivable that sulphur may have come from the nearby moon Io, where sulphur and other volcanic elements are abundant. Secondly, volcanic eruptions in Europa's seafloor may have brought sulphur to the surface. Can waste products rising from bacterial colonies beneath the icy surface be a third alternative significant factor in the sulphur patches on the Europan surface? Provided that microorganisms on Europa have the same biochemical pathways as those on Earth, over geologic time it is possible that autochthonous microbes can add substantially to the sulphur deposits on the surface of Europa. We discuss possible interpretations of the non-water-ice elements (especially the sulphur compound mercaptan) in the context of the studies for future missions. To achieve reliable biosignatures it seems essential to go back to Europa. Our work highlights the type of biogenic signatures that can be searched for when probing Europa's icy and patchy surface. (author)

Formation and Atmosphere of Complex Organic Molecules of the HH 212 Protostellar Disk

Energy Technology Data Exchange (ETDEWEB)

Lee, Chin-Fei; Ho, Paul T. P.; Hirano, Naomi; Shang, Hsien [Academia Sinica Institute of Astronomy and Astrophysics, P.O. Box 23-141, Taipei 106, Taiwan (China); Li, Zhi-Yun [Astronomy Department, University of Virginia, Charlottesville, VA 22904 (United States); Zhang, Qizhou, E-mail: cflee@asiaa.sinica.edu.tw [Harvard-Smithsonian Center for Astrophysics, 60 Garden Street, Cambridge, MA 02138 (United States)

2017-07-01

HH 212 is a nearby (400 pc) Class 0 protostellar system recently found to host a “hamburger”-shaped dusty disk with a radius of ∼60 au, deeply embedded in an infalling-rotating flattened envelope. We have spatially resolved this envelope-disk system with the Atacama Large Millimeter/submillimeter Array at up to ∼16 au (0.″04) resolution. The envelope is detected in HCO{sup +} J = 4–3 down to the dusty disk. Complex organic molecules (COMs) and doubly deuterated formaldehyde (D{sub 2}CO) are detected above and below the dusty disk within ∼40 au of the central protostar. The COMs are methanol (CH{sub 3}OH), deuterated methanol (CH{sub 2}DOH), methyl mercaptan (CH{sub 3}SH), and formamide (NH{sub 2}CHO, a prebiotic precursor). We have modeled the gas kinematics in HCO{sup +} and COMs and found a centrifugal barrier (CB) at a radius of ∼44 au, within which a Keplerian rotating disk is formed. This indicates that HCO{sup +} traces the infalling-rotating envelope down to the CB and COMs trace the atmosphere of a Keplerian rotating disk within the CB. The COMs are spatially resolved for the first time, both radially and vertically, in the atmosphere of a disk in the earliest, Class 0 phase of star formation. Our spatially resolved observations of COMs favor their formation in the disk rather than a rapidly infalling (warm) inner envelope. The abundances and spatial distributions of the COMs provide strong constraints on models of their formation and transport in low-mass star formation.

Inactivation of microorganisms by UV-treatment of must and wine

Directory of Open Access Journals (Sweden)

Durner Dominik

2017-01-01

Full Text Available The objective was to investigate the applicability of UV-C technology to inactivate yeasts and bacteria in must and wine. Experiments were carried out in vintage 2016 with Riesling musts of different quality containing their natural microflora. Yeasts were tested more resistant to UV-C energy than bacteria. Saccharomyces cerevisiae showed higher tolerance against UV-C irradiation than Hanseniaspora uvarum facilitating new opportunities to control spontaneous fermentations. However, inactivation efficacy was strongly dependent on turbidity of musts and the initial degree of contamination suggesting a shadowing effect of individual germs. Compared with thermal pasteurization, UV-C treatment of must with 1 kJ/L showed similar effects in germ-reduction. While thermal pasteurization significantly decreased aroma precursors in musts, UV-C treatment did not change concentrations of glycosidically-bound C6-alcohols, monoterpenes and C13-norisoprenoids as shown by GC-MS analysis. Applying UV-C technology in wines, it was possible to irreversibly stop ongoing alcoholic fermentation indicating that UV-C treatment is capable to replace SO2 addition to produce wines with residual sugar. Besides inactivation power, UV-C is known for its ability to form powerful off-flavours such as methional or methanethiol. Sensory analysis revealed that the application of UV-C at doses < 2 kJ/L in must is uncritical. However, applying UV-C after alcoholic fermentation can result in rising concentrations of mercaptans already at doses < 1 kJ/L. In this context, compounds such as caftaric acid, riboflavin and dissolved oxygen are thought to positively contribute to the UV-induced formation of off-flavours in wine.

Sweet smell of success -- and safety

Energy Technology Data Exchange (ETDEWEB)

Harrison, L.

2005-02-01

Gas scavenger is a commonly used term for a product that reacts with hydrogen sulfide and converts it to another form that no longer presents the same toxicity. This paper describes the DVS 6000, a non-flammable, non-corrosive zinc-based product that converts hydrogen sulfide mostly to zinc sulfide, a harmless substance in the form of a very fine precipitate. It is used to to eliminate hydrogen sulfide and mercaptans in gas streams in truck-mounted scrubbers, bubble towers, contaminated storage tanks and vessels, and for direct injections into gas streams. The resulting zinc sulfide is more environmentally friendly than hydrogen sulfide, or other competing scavenger products, and can be disposed of downhole, as with any other scavenger. It has a freezing point below -- 45 degrees C, therefore it is usable in the Arctic. It can be transported by air, sea, or land (i.e. it is not subject to regulation under the Transportation of Dangerous Goods Act), and can be used right at the wellhead or at the gas plant. DVS 6000 is a clear amber-coloured liquid, has a mild odour, and is safer to use than ammonia (used in other scavenger products) since it does much less damage to the lungs and nasal passages if inhaled. Developers of DVS 6000, Diversified Industries Ltd., are currently conducting field trials in conjunction with major end-users for application of the product in steam purging and cleaning, direct injection into pipelines, downhole drilling fluids and treatment of stored reserves in liquid hydrocarbons containing hydrogen sulfide. Indications are that DVS 6000 will be in high demand domestically and internationally.

In vitro effects of Melaleuca alternifolia essential oil on growth and production of volatile sulphur compounds by oral bacteria

Directory of Open Access Journals (Sweden)

Talita Signoreti GRAZIANO

Full Text Available ABSTRACT Objective Halitosis can be caused by microorganisms that produce volatile sulphur compounds (VSCs, which colonize the surface of the tongue and subgingival sites. Studies have reported that the use of natural products can reduce the bacterial load and, consequently, the development of halitosis. The aim of this study was to evaluate the antimicrobial activity of the essential oil of Melaleuca alternifolia on the growth and volatile sulphur compound (VSC production of oral bacteria compared with chlorhexidine. Material and Methods The effects of these substances were evaluated by the Minimum Inhibitory Concentration (MIC and Minimum Bactericidal Concentration (MBC in planktonic cultures of Porphyromonas gingivalis and Porphyromonas endodontalis. In addition, gas chromatography analyses were performed to measure the concentration of VSCs from bacterial cultures and to characterize M. alternifolia oil components. Results The MIC and MBC values were as follows: M. alternifolia - P. gingivalis (MIC and MBC=0.007%, P. endodontalis (MIC and MBC=0.007%=0.5%; chlorhexidine - P. gingivalis and P. endodontalis (MIC and MBC=1.5 mg/mL. M. alternifolia significantly reduced the growth and production of hydrogen sulfide (H2S by P. gingivalis (p<0.05, ANOVA-Dunnet and the H2S and methyl mercaptan (CH3SH levels of P. endodontalis (p<0.05, ANOVA-Dunnet. Chlorhexidine reduced the growth of both microorganisms without altering the production of VSC in P. endodontalis. For P. gingivalis, the production of H2S and CH3SH decreased (p<0.05, ANOVA-Dunnet. Conclusion M. alternifolia can reduce bacterial growth and VSCs production and could be used as an alternative to chlorhexidine.

The use of modified tyre derived fuel for compression ignition engines.

Science.gov (United States)

Pilusa, T J

2017-02-01

This study investigated physical and chemical modification of tyre-derived fuel oil (TDFO) obtained from pyrolysis of waste tyres and rubber products for application as an alternative fuel for compression ignition engines (CIE's). TDFO collected from a local waste tyre treatment facility was refined via a novel "oxidative gas-phase fractional distillation over 13× molecular sieves" to recover the light to medium fractions of the TDFO while oxidising and capturing some sulphur compounds in a gas phase. This was followed by desulphurization and chemical modification to improve cetane number, kinematic viscosity and fuel stability. The resulting fuel was tested in an ADE407T truck engine to compare its performance with petroleum diesel fuel. It was discovered that gas phase oxidative fractional distillation reduces the low boiling point sulphur compounds in TDFO such as mercaptans. Using petroleum diesel fuel as a reference, it was observed that the produced fuel has a lower cetane number, flash point and viscosity. On storage the fuel tends to form fibrous microstructures as a result of auto-oxidation of asphaltenes present in the fuel. Mixtures of alkyl nitrate, vinyl acetate, methacrylic anhydride, methyl-tert butyl ether, n-hexane and n-heptane were used to chemically modify the fuel in accordance with the minimum fuel specifications as per SANS 342. The engine performance tests results did not show any sign of engine ceasing or knocking effect. The power-torque trend was very consistent and compared well with petroleum diesel fuelled engine. The levels of total sulphur are still considerably high compared to other cleaner fuel alternatives derived from zero sulphur sources. Copyright © 2016. Published by Elsevier Ltd.

Electrochemistry and spectro-electrochemistry of dithizonatophenylmercury(II)

International Nuclear Information System (INIS)

Eschwege, Karel G. von; As, Lydia van; Swarts, Jannie C.

2011-01-01

Graphical abstract: Display Omitted Highlights: → CV and spectroelectrochemistry of dithizone and PhHgHDz, 3, is presented. → CV shows 3 has stable metal thioether (Hg-S-C), 1 oxidation and two reductions. → 3 is photochromic (t 1/2, relaxation = 1300 s). → Electrochemistry of ground and photo-activated 3 is identical. → Spectroelectrochemistry of 3 highlights electrochromism. - Abstract: The reactions between dithizone (H 2 Dz, (1)) or potassium dithizonate (K + HDz - , (2)) and phenylmercury(II) chloride gives PhHg(HDz), (3). Complex (3) is photochromic. In dichloromethane, the blue photo-exited state of (3) exhibits a first order relaxation process to regenerate the orange ground state with rate constant 0.00053 s -1 . The half life of this relaxation is ca. 1300 s. Electrochemically, on cyclic voltammetry time scale, the oxidations of (1) and (3) are different. A comparative voltammetric and spectro-electrochemical study of (1) and (3) in CH 2 Cl 2 containing 0.1 mol dm -3 [N( n Bu) 4 ][B(C 6 F 5 ) 4 ] revealed that the mercapto group of (1) can be oxidised in two one-electron transfer steps. A disulphide is first produced and then in a second oxidation step, HDz + is formed. In contrast, complex (3) shows only one ligand-based oxidation step. Upon complexation with phenylmercury the free mercaptan group of (1) becomes a stable 'metal thioether', Hg-S-C, which effectively prevents disulphide formation in (3) upon electrochemical oxidation. Both (1) and (3) shows two reduction steps. The electrochemical fingerprint of blue photo-excited (3) is identical to that of the orange ground state as no new functional groups are introduced upon irradiation; only bond rotation occurs. The different electronic spectra for each of the redox states of (3), obtained from spectro-electrochemical measurements, revealed that only the (3)/(3 - ) couple exhibits electrochromic properties.

Control of oral malodour by dentifrices measured by gas chromatography.

Science.gov (United States)

Newby, Evelyn E; Hickling, Jenneth M; Hughes, Francis J; Proskin, Howard M; Bosma, Marylynn P

2008-04-01

To evaluate the effect of toothpaste treatments on levels of oral volatile sulphur compounds (VSCs) measured by gas chromatography in two clinical studies. These were blinded, randomised, controlled, crossover studies with 16 (study A) or 20 (study B) healthy volunteers between the ages of 19-54. Study A: breath samples were collected at baseline, immediately and lhr after brushing. Four dentifrices (Zinc A, Zinc B, commercially available triclosan dentifrice and zinc free control) were evaluated. Study B: breath samples were collected at baseline, immediately, 1, 2, 3 and 7 hours after treatment. Subjects consumed a light breakfast then provided an additional breath sample between baseline assessment and treatment. Two dentifrices (gel-to-foam and a commercially available triclosan dentrifrice) were evaluated. Breath samples were collected in syringes and analysed for VSCs (hydrogen sulphide, methyl mercaptan and Total VSCs) utilising gas chromatography (GC) with flame photometric detection. Study A: immediately after treatment, a statistically significant reduction in VSCs from baseline was observed for Zinc A product only. A statistically significant reduction in VSCs from baseline was observed after 1 hour for all products. Both zinc products exhibited a significantly greater reduction from baseline VSCs than Colgate Total and Control at all time points. Study B: a statistically significant reduction in VSCs from baseline was observed at all time points for both products. The gel-to-foam product exhibited significantly greater reduction from baseline Total VSC concentration than Colgate Total at all time points from 1 hour post-treatment. Control of oral malodour by toothpaste treatment, evaluated as VSC levels using GC, has been demonstrated. Zinc is effective at reducing VSCs and the efficacy of zinc is formulation dependent. A gel-to-foam dentifrice was more effective at reducing VSCs than Colgate Total up to 7 hours.

Emission of volatile sulfur compounds during composting of municipal solid waste (MSW)

International Nuclear Information System (INIS)

Zhang, Hongyu; Schuchardt, Frank; Li, Guoxue; Yang, Jinbing; Yang, Qingyuan

2013-01-01

Highlights: ► We compare the volatile sulfur compounds (VSCs) emissions during three types of municipal solid wastes (MSWs) composting. ► The VSCs released from the kitchen waste composting was significantly higher than that from 15–80 mm fraction of MSW. ► Among the five VSCs, H 2 S was the most abundant compound with 39.0–43.0% of total VSCs released. ► Addition of 20% cornstalks could significantly reduce the VSCs emissions during kitchen waste composting. - Abstract: Volatile sulfur compounds (VSCs) are the main source for malodor from composting plants. In this study, the VSCs generated from composting of 15–80 mm municipal solid waste (T0), kitchen waste (T1) and kitchen waste mixed dry cornstalks (T2) were measured in 60 L reactors with forced aeration for a period of 30 days. The VSCs detected in all treatments were hydrogen sulfide (H 2 S), methyl mercaptan (MM), dimethyl sulfide (DMS), carbon bisulfide (CS 2 ) and dimethyl disulfide (DMDS). Over 90% of the VSCs emissions occurred during the first 15 days, and reached their peak values at days 4–7. The emission profiles of five VSCs species were significantly correlated with internal materials temperature and outlet O 2 concentration (p −1 (dry matter) for T0, T1 and T2, respectively. Among the five VSCs, H 2 S was the most abundant compound with 39.0–43.0% of total VSCs released. Composting of kitchen waste from separate collection posed a negative influence on the VSC and leachate production because of its high moisture content. An addition of dry cornstalks at a mixing ratio of 4:1 (wet weight) could significantly reduce the VSCs emissions and avoid leachate. Compared to pure kitchen waste, VSCs were reduced 66.8%

Dynamic olfactometry and GC–TOFMS to monitor the efficiency of an industrial biofilter

Energy Technology Data Exchange (ETDEWEB)

Gutiérrez, M.C.; Martín, M.A. [University of Cordoba, Department of Inorganic Chemical and Chemical Engineering, Campus Universitario de Rabanales, Carretera N-IV, km 396, Edificio Marie Curie, 14071 Córdoba (Spain); Pagans, E.; Vera, L. [Odournet SL, Parc de Recerca UAB, Edificio Eureka, Espacio P2M2, 08193, Bellaterra, Cerdanyola del Vallès, Barcelona (Spain); García-Olmo, J. [NIR/MIR Spectroscopy Unit, Central Service for Research Support (SCAI), University of Cordoba, Campus de Rabanales, 14071 Cordoba (Spain); Chica, A.F., E-mail: afchica@uco.es [University of Cordoba, Department of Inorganic Chemical and Chemical Engineering, Campus Universitario de Rabanales, Carretera N-IV, km 396, Edificio Marie Curie, 14071 Córdoba (Spain)

2015-04-15

Biofiltration is the most widely used technique for eliminating odours in waste treatment plants. Volatile organic compounds (VOCs) are among the odorous compounds emitted by waste management plants, and serve as variables to measure odour emissions depending on the type of aeration process used. In this work, we assess the performance of an industrial-scale biofilter where composting is the main source of VOCs and odour emissions. Dynamic olfactometry is the sensorial technique used to determine odour concentration, while gas chromatography–time of flight-mass spectrometry (GC–TOFMS) is used to perform the chemical characterization. This work examines a total of 82 compounds belonging to 15 odorous families of VOCs, particularly mercaptans, sulphur-containing compounds, alcohols and terpenes, among others. Principal component analysis (PCA) is used to assess the influence of each of these families of VOCs on the total variance of the measure with regard to both the input and output flow of the biofilter. Finally, partial least-squares (PLS) regression is used to estimate the odour concentration in each of the samples taken at the inlet and outlet of the biofilter in each of the samples based on the chemical information provided by chromatographic analysis. The study shows that there is an adequate correlation (r = 0.9751) between real and estimated odour concentrations, both of which are expressed in European odour units per cubic metre (ou{sub E}·m{sup −3}). - Highlights: • Odour and VOC removal by industrial biofilter was evaluated. • Dynamic olfactometry and GC-TOF MS were the techniques used. • The compost aeration mode was considered in this study. • The influence of 15 VOC families on sample variance was demonstrated by PCA. • Odour concentration was predicted from selected chromatographic information by PLS.

Reduced sulfur compounds in gas from construction and demolition debris landfills.

Science.gov (United States)

Lee, Sue; Xu, Qiyong; Booth, Matthew; Townsend, Timothy G; Chadik, Paul; Bitton, Gabriel

2006-01-01

The biological conversion of sulfate from disposed gypsum drywall to hydrogen sulfide (H(2)S) in the anaerobic environment of a landfill results in odor problems and possible health concerns at many disposal facilities. To examine the extent and magnitude of such emissions, landfill gas samples from wells, soil vapor samples from the interface of the waste and cover soil, and ambient air samples, were collected from 10 construction and demolition (C&D) debris landfills in Florida and analyzed for H(2)S and other reduced sulfur compounds (RSC). H(2)S was detected in the well gas and soil vapor at all 10 sites. The concentrations in the ambient air above the surface of the landfill were much lower than those observed in the soil vapor, and no direct correlation was observed between the two sampling locations. Methyl mercaptan and carbonyl sulfide were the most frequently observed other RSC, though they occurred at smaller concentrations than H(2)S. This research confirmed the presence of H(2)S at C&D debris landfills. High concentrations of H(2)S may be a concern for employees working on the landfill site. These results indicate that workers should use proper personal protection at C&D debris landfills when involved in excavation, landfill gas collection, or confined spaces. The results indicate that H(2)S is sufficiently diluted in the atmosphere to not commonly pose acute health impacts for these landfill workers in normal working conditions. H(2)S concentrations were extremely variable with measurements occurring over a very large range (from less than 3 ppbv to 12,000 ppmv in the soil vapor and from less than 3 ppbv to 50 ppmv in ambient air). Possible reasons for the large intra- and inter-site variability observed include waste and soil heterogeneities, impact of weather conditions, and different site management practices.

Protective Behaviour of Citizens to Transport Accidents Involving Hazardous Materials: A Discrete Choice Experiment Applied to Populated Areas nearby Waterways.

Directory of Open Access Journals (Sweden)

Esther W de Bekker-Grob

Full Text Available To improve the information for and preparation of citizens at risk to hazardous material transport accidents, a first important step is to determine how different characteristics of hazardous material transport accidents will influence citizens' protective behaviour. However, quantitative studies investigating citizens' protective behaviour in case of hazardous material transport accidents are scarce.A discrete choice experiment was conducted among subjects (19-64 years living in the direct vicinity of a large waterway. Scenarios were described by three transport accident characteristics: odour perception, smoke/vapour perception, and the proportion of people in the environment that were leaving at their own discretion. Subjects were asked to consider each scenario as realistic and to choose the alternative that was most appealing to them: staying, seeking shelter, or escaping. A panel error component model was used to quantify how different transport accident characteristics influenced subjects' protective behaviour.The response was 44% (881/1,994. The predicted probability that a subject would stay ranged from 1% in case of a severe looking accident till 62% in case of a mild looking accident. All three transport accident characteristics proved to influence protective behaviour. Particularly a perception of strong ammonia or mercaptan odours and visible smoke/vapour close to citizens had the strongest positive influence on escaping. In general, 'escaping' was more preferred than 'seeking shelter', although stated preference heterogeneity among subjects for these protective behaviour options was substantial. Males were less willing to seek shelter than females, whereas elderly people were more willing to escape than younger people.Various characteristics of transport accident involving hazardous materials influence subjects' protective behaviour. The preference heterogeneity shows that information needs to be targeted differently depending on

Creation of anticorrosion coatings for contact devices of rectifying columns

Directory of Open Access Journals (Sweden)

KATAMANOV Vladimir Leonidovich

2018-02-01

Full Text Available Today the main corrosion protection methods applied in contact devices of rectifying oil processing equipment, in particular, in mesh nozzles made of stainless steel, under relatively high temperatures (150–250оC and in the presence of aggressive components in oil raw materials (hydrogen sulfide, sulfides, mercaptans, other sulphurous compounds, chloride ions, organochlorine connections, water are to use special alloys as protecting covers as well as corrosion inhibitors that reduce corrosion action of hostile environment. At the same time, the disadvantages of the majority of these methods concern high operational costs, insufficient efficiency or protection ability designed only for a certain factor, but not for combination of them. In this regard corrosion resistance of mesh contact devices made of stainless steel (brand SUS 321 has been studied on three types of samples: alloy wire, welded grid, thin leaf. Titanium nitride (TiN and metallic coatings from nickel (Ni, titanium (Ti and chrome (Cr were used as anticorrosion coatings for the mentioned samples. These coverings were applied on samples in two ways: by means of electrolytic method and vacuum ion-plasma dusting. It was determined that optimal coating thickness is 10–15 microns as it is the thickness at which the produced films possess sufficient plasticity and do not exfoliate from the surface of the corresponding corrosion-proof alloy. The research of corrosion of samples of stainless steel SUS 321 with applied coverings and without them was performed by immersing the samples into compositions that contain oil as well as into the modeling hostile oil-containing environment. As a result of the conducted researches it was determined that the protecting covers of chrome and titanium nitride applied with vacuum ion-plasma dusting method are the most effective coatings from the point of view of anticorrosive protection for mesh contact devices of stainless steel used in rectifying

Kinetic modeling of the thermal evolution of crude oils in sedimentary basins; Modelisation cinetique de l'evolution thermique des petroles dans les gisements

Energy Technology Data Exchange (ETDEWEB)

Bounaceur, R.

2001-01-15

The aim of this work is to obtain a better understanding of the reactions involved in the thermal cracking of crude oil in sedimentary basins, and to study its kinetics as a function of temperature and pressure. We study the kinetics of pyrolysis of alkanes at low temperature, high pressure and high conversion and we propose three methods of reduction of the corresponding mechanisms. Several compounds having an inhibiting or accelerating effect on the rate of decomposition of alkanes were also studied. This research led to the construction of a general kinetic model of 5200 elementary steps representing the pyrolysis of a complex mixture of 52 molecules belonging to various chemical families: 30 linear alkanes (from CH{sub 4} to C{sub 30}H{sub 62}), 10 branched-chain alkanes (including pristane and phytane), 2 naphthenes (propyl-cyclo-pentane and propyl-cyclohexane), tetralin, 1-methyl-indan, 4 aromatics (benzene, toluene, butyl-benzene and decyl-benzene), 3 hetero-atomic compounds (a disulfide, a mercaptan and H{sub 2}S). This model is compared to experimental data coming from the pyrolysis of two oils: one from the North Sea and the other from Pematang. The results obtained show a good agreement between the experimental and simulated values. Then, we simulated the cracking of these two oils by using the following burial scenario: initial temperature of 160 degrees, 50 m per million years (ma) in a constant geothermal gradient of 30 degrees C/km, implying a heating rate of 1.5 degrees C/ma. Under these conditions, our model shows that these two oils start to crack only towards 210-220 degrees C and that their time of half-life corresponds to a temperature around 230-240 degrees C. The model also makes it possible to simulate the evolution of geochemical parameters such as the GOR, the API degree... (author)

Characterisation and cleaning of biogas from sewage sludge for biomethane production.

Science.gov (United States)

Paolini, Valerio; Petracchini, Francesco; Carnevale, Monica; Gallucci, Francesco; Perilli, Mattia; Esposito, Giulio; Segreto, Marco; Occulti, Leandro Galanti; Scaglione, Davide; Ianniello, Antonietta; Frattoni, Massimiliano

2018-07-01

This study investigates the conversion of sewage sludge from wastewater treatment plants (WWTP) into biomethane for automotive fuel or grid injection. A prototype plant was monitored in Northern Italy, based on vacuum swing adsorption (VSA) on synthetic zeolite 13×: this biogas upgrading method is similar to pressure swing adsorption (PSA) and commonly used for other kinds of biomass. Measurements of biogas inlet, biomethane outlet and off-gas were performed including CH 4 , CO 2 , CO, H 2 , O 2 , N 2 , HCl, HF, NH 3 , H 2 S and volatile organic compounds (VOCs). Critical levels were observed in the biogas for of H 2 S and HCl, whose concentrations were 1570 and 26.8 mg m -3 , respectively. On the other hand, the concentration of halogenated VOCs (including tetrachloroethylene and traces of perfluoroalkilated substances, PFAS) and mercaptans were relatively low. A simultaneous and reversible adsorption on 13× zeolite was achieved for H 2 S and CO 2 , and carbon filters played a minor role in desulfurisation. The presence of HCl is due to clarifying agents, and its removal is necessary in order to meet the required biomethane characteristics: an additional carbon-supported basic adsorbent was successfully used to remove this contaminant. This study also highlights the interference of CO 2 towards HCl if sampling is performed in compliance with the new EU standard for biomethane. High total volatile silicon (TVS) was confirmed in sewage sludge biogas, with a major contribution of siloxane D5: the suitability of this compound as an indicator of total siloxanes is discussed. Results demonstrate that volatile methyl siloxanes (VMS) do not represent a critical issue for the VSA upgrading methodology. Copyright © 2018 Elsevier Ltd. All rights reserved.

Calibration transfer between electronic nose systems for rapid In situ measurement of pulp and paper industry emissions

Energy Technology Data Exchange (ETDEWEB)

Deshmukh, Sharvari [CSIR-National Environmental Engineering and Research Institute, Nagpur (India); Department of Instrumentation and Electronics Engineering, Jadavpur University, Kolkata (India); Kamde, Kalyani [CSIR-National Environmental Engineering and Research Institute, Nagpur (India); Jana, Arun [Center for Development of Advance Computing, Kolkata (India); Korde, Sanjivani [CSIR-National Environmental Engineering and Research Institute, Nagpur (India); Bandyopadhyay, Rajib [Department of Instrumentation and Electronics Engineering, Jadavpur University, Kolkata (India); Sankar, Ravi [Center for Development of Advance Computing, Kolkata (India); Bhattacharyya, Nabarun, E-mail: nabarun.bhattacharya@cdac.in [Center for Development of Advance Computing, Kolkata (India); Pandey, R.A., E-mail: ra_pandey@neeri.res.in [CSIR-National Environmental Engineering and Research Institute, Nagpur (India)

2014-09-02

Highlights: • E-nose developed for obnoxious emissions measurement at pulp and paper industrial site. • ANN model developed for prediction of (CH{sub 3}){sub 2}S, (CH{sub 3}){sub 2}S{sub 2}, CH{sub 3}SH and H{sub 2}S concentration. • Calibration transfer methodology developed for transfer between two e-nose instruments. • Box–Behnken design and robust regression used for calibration transfer. • Results show effective transfer of training model from one e-nose system to other. - Abstract: Electronic nose systems when deployed in network mesh can effectively provide a low budget and onsite solution for the industrial obnoxious gaseous measurement. For accurate and identical prediction capability by all the electronic nose systems, a reliable calibration transfer model needs to be implemented in order to overcome the inherent sensor array variability. In this work, robust regression (RR) is used for calibration transfer between two electronic nose systems using a Box–Behnken (BB) design. Out of the two electronic nose systems, one was trained using industrial gas samples by four artificial neural network models, for the measurement of obnoxious odours emitted from pulp and paper industries. The emissions constitute mainly of hydrogen sulphide (H{sub 2}S), methyl mercaptan (MM), dimethyl sulphide (DMS) and dimethyl disulphide (DMDS) in different proportions. A Box–Behnken design consisting of 27 experiment sets based on synthetic gas combinations of H{sub 2}S, MM, DMS and DMDS, were conducted for calibration transfer between two identical electronic nose systems. Identical sensors on both the systems were mapped and the prediction models developed using ANN were then transferred to the second system using BB–RR methodology. The results showed successful transmission of prediction models developed for one system to other system, with the mean absolute error between the actual and predicted concentration of analytes in mg L{sup −1} after calibration

Identificação e quantificação de voláteis de café através de cromatografia gasosa de alta resolução / espectrometria de massas empregando um amostrador automático de "headspace" Identification and quantification of coffee volatile components through high resolution gas chromatoghaph/mass spectrometer using a headspace automatic sampler

Directory of Open Access Journals (Sweden)

Leonardo César AMSTALDEN

2001-01-01

Full Text Available Usando um amostrador automático, os "headspaces" de três marcas comerciais de café torrado e moído foram analisados qualitativa e quantitativamente quanto a composição dos voláteis responsáveis pelo aroma através da técnica de cromatografia gasosa/espectrometria de massas. Uma vez que a metodologia não envolveu isolamento ou concentração dos aromas, suas proporções naturais foram mantidas, além de simplificar o preparo das amostras. O emprego do amostrador automático permitiu também boa resolução dos picos cromatográficos sem o emprego de criogenia, contribuindo para redução no tempo de análise. Noventa e um componentes puderam ser identificados, sendo que alguns compostos conhecidos como presentes em café como o dimetilsulfeto, metional e furfuril mercaptana não foram detectados. Os voláteis presentes em maior concentração puderam ser quantificados com o auxílio de dois padrões internos. A técnica se provou viável, tanto para caracterização como para quantificação de voláteis de café.Employing an automatic headspace sampler, the headspaces of three commercial brands of ground roasted coffee were qualitatively and quantitatively analyzed by gas chromatography / mass spectrometry. Since the methodology did not involve aroma isolation or concentration, their natural proportions were maintained, providing a more accurate composition of the flavors, and simplifying sample preparation. The automatic sampler allowed good resolution of the chromatographic peaks without cryofocusing the samples at the head of the column during injection, reducing analysis time. Ninety one compounds were identified and some known coffee volatiles, such as dimethyl sulphide, methional and furfuryl mercaptan were not detected. The more concentrated volatiles could be identified using two internal standards. The technique proved viable, for both characterization and for quantification of coffee volatiles.

Avaliação da incorporação de resíduo de poli(etileno-co-acetato de vinila em borracha nitrílica Evaluation of waste poly(ethylene-co-vinyl incorporation in nitrile rubber

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Viviane X. Moreira

2003-01-01

Full Text Available A influência do resíduo de poli(etileno-co-acetato de vinila (EVAR no desempenho mecânico de composições vulcanizadas de NBR foi estudada. A concentração ótima de EVAR, a qual apresentou maior valor de tensão na ruptura, foi de 50 phr. Além disso, a influência do EVA e do EVAR funcionalizado com grupos tióis (EVALSH e do EVAR modificado com anidrido maleico (EVARCO como agentes compatibilizantes foi estudada. O copolímero EVALSH atuou como acelerador no processo de vulcanização, sendo observado um decréscimo do tempo de vulcanização. Uma melhora na resistência ao envelhecimento também foi observada. A adição de 10 phr de EVARCO resultou na redução do tempo de vulcanização e em uma melhora na maior parte das propriedades avaliadas. As propriedades termodinâmico-mecânicas foram avaliadas por análises de DMTA. Os estudos da interação entre a fase dispersa e a fase matriz foram realizados utilizando-se microscopia eletrônica de varredura (MEV.The influence of poly(ethylene-co-vinyl acetate (EVA waste (EVAR on the mechanical performance of NBR vulcanisates compounds was studied. The optimum concentration of EVAR, which has presented higher ultimate tensile stress, was found at 50 phr. In addition, the influence of EVA and EVAR functionalized with mercaptan groups (EVALSH and EVAR functionalized with maleic anidride (EVARCO as compatibilizing agents was studied. The copolymer EVALSH acted as accelerator for the curing system, since a decreasing of the curing time was observed. An improvement of ageing resistance was also observed. The addition of EVARCO resulted in a reduction of the curing time and an improvement of most of evaluated properties. The thermodynamic-mechanic properties were investigated by DMTA analysis. The studies on the interaction between dispersed phase and matrix were performed by scanning electron microscopy (SEM.

The bonding of heavy metals on nitric acid-etched coal fly ashes functionalized with 2-mercaptoethanol or thioglycolic acid

International Nuclear Information System (INIS)

Muñoz, M.I.; Aller, A.J.; Littlejohn, D.

2014-01-01

Coal fly ash is a waste by-product of the coal fire industry, which generates many environmental problems. Alternative uses of this material would provide efficient solutions for this by-product. In this work, nitric acid-etched coal fly ash labelled with 2-mercaptoethanol or thioglycolic acid was assessed for retention of Al(III), As(III), Cu(II), Cd(II), Fe(III), Mn(II), Hg(II), Ni(II), Pb(II) and Zn(II) ions. The bonding characteristics between the organic compounds with the solid support, as well as with the metal ions, were evaluated using various surface analytical techniques. Visualization of the organically-functionalized coal fly ash particle was possible using scanning electron microscopy (SEM), while the elemental composition of the functionalized material, before and after retention of the metal ions, was obtained by energy dispersive (ED)-X ray spectrometry (XRS) and electrothermal atomic absorption spectrometry (ETAAS). Fourier transform infrared (FT-IR) spectrometry and Raman spectrometry were used to obtain information about the functional groups. It was found that some metal(oid) ions (As, Ni, Pb, Zn) were coordinated through the mercaptan group, while other metal(oid)s (Al, Cd, Cu, Fe, Hg, Mn) were apparently bonded to oxygen atoms. A low-cost and effective solid phase retention system for extraction of heavy metals from aqueous solutions was thus developed. - Graphical abstract: Nitric acid-etched coal fly ash labelled with 2-mercaptoethanol or thioglycolic acid was intended for the retention of heavy metals. The bonding characteristics between the organic compounds with the solid support, as well as with the metal ions, were evaluated using surface analytical techniques. - Highlights: • Coal fly ashes were organically-functionalized. • Organically-functionalized coal fly ashes were spectrometrically characterized. • Organically-functionalized coal fly ashes can be used as an effective solid sorbent for metal(oid)s. • This retention

Calibration transfer between electronic nose systems for rapid In situ measurement of pulp and paper industry emissions

International Nuclear Information System (INIS)

Deshmukh, Sharvari; Kamde, Kalyani; Jana, Arun; Korde, Sanjivani; Bandyopadhyay, Rajib; Sankar, Ravi; Bhattacharyya, Nabarun; Pandey, R.A.

2014-01-01

Highlights: • E-nose developed for obnoxious emissions measurement at pulp and paper industrial site. • ANN model developed for prediction of (CH 3 ) 2 S, (CH 3 ) 2 S 2 , CH 3 SH and H 2 S concentration. • Calibration transfer methodology developed for transfer between two e-nose instruments. • Box–Behnken design and robust regression used for calibration transfer. • Results show effective transfer of training model from one e-nose system to other. - Abstract: Electronic nose systems when deployed in network mesh can effectively provide a low budget and onsite solution for the industrial obnoxious gaseous measurement. For accurate and identical prediction capability by all the electronic nose systems, a reliable calibration transfer model needs to be implemented in order to overcome the inherent sensor array variability. In this work, robust regression (RR) is used for calibration transfer between two electronic nose systems using a Box–Behnken (BB) design. Out of the two electronic nose systems, one was trained using industrial gas samples by four artificial neural network models, for the measurement of obnoxious odours emitted from pulp and paper industries. The emissions constitute mainly of hydrogen sulphide (H 2 S), methyl mercaptan (MM), dimethyl sulphide (DMS) and dimethyl disulphide (DMDS) in different proportions. A Box–Behnken design consisting of 27 experiment sets based on synthetic gas combinations of H 2 S, MM, DMS and DMDS, were conducted for calibration transfer between two identical electronic nose systems. Identical sensors on both the systems were mapped and the prediction models developed using ANN were then transferred to the second system using BB–RR methodology. The results showed successful transmission of prediction models developed for one system to other system, with the mean absolute error between the actual and predicted concentration of analytes in mg L −1 after calibration transfer (on second system) being 0.076, 0

Emission of volatile sulfur compounds during composting of municipal solid waste (MSW)

Energy Technology Data Exchange (ETDEWEB)

Zhang, Hongyu [Beijing Building Materials Academy of Science Research/State Key Laboratory of Solid Waste Reuse for Building Material, Beijing 100041 (China); College of Resources and Environment Sciences, China Agricultural University, Beijing 100094 (China); Schuchardt, Frank [Johann Heinrich von Thuenen-Institute, Institute of Agricultural Technology and Biosystems Engineering, Bundesallee 50, 38116 Braunschweig (Germany); Li, Guoxue, E-mail: ligx@cau.edu.cn [College of Resources and Environment Sciences, China Agricultural University, Beijing 100094 (China); Yang, Jinbing; Yang, Qingyuan [College of Resources and Environment Sciences, China Agricultural University, Beijing 100094 (China)

2013-04-15

Highlights: ► We compare the volatile sulfur compounds (VSCs) emissions during three types of municipal solid wastes (MSWs) composting. ► The VSCs released from the kitchen waste composting was significantly higher than that from 15–80 mm fraction of MSW. ► Among the five VSCs, H{sub 2}S was the most abundant compound with 39.0–43.0% of total VSCs released. ► Addition of 20% cornstalks could significantly reduce the VSCs emissions during kitchen waste composting. - Abstract: Volatile sulfur compounds (VSCs) are the main source for malodor from composting plants. In this study, the VSCs generated from composting of 15–80 mm municipal solid waste (T0), kitchen waste (T1) and kitchen waste mixed dry cornstalks (T2) were measured in 60 L reactors with forced aeration for a period of 30 days. The VSCs detected in all treatments were hydrogen sulfide (H{sub 2}S), methyl mercaptan (MM), dimethyl sulfide (DMS), carbon bisulfide (CS{sub 2}) and dimethyl disulfide (DMDS). Over 90% of the VSCs emissions occurred during the first 15 days, and reached their peak values at days 4–7. The emission profiles of five VSCs species were significantly correlated with internal materials temperature and outlet O{sub 2} concentration (p < 0.05). Total emissions of the VSCs were 216.1, 379.3 and 126.0 mg kg{sup −1} (dry matter) for T0, T1 and T2, respectively. Among the five VSCs, H{sub 2}S was the most abundant compound with 39.0–43.0% of total VSCs released. Composting of kitchen waste from separate collection posed a negative influence on the VSC and leachate production because of its high moisture content. An addition of dry cornstalks at a mixing ratio of 4:1 (wet weight) could significantly reduce the VSCs emissions and avoid leachate. Compared to pure kitchen waste, VSCs were reduced 66.8%.

Volatile compounds of Domiati cheese made from buffaloe's milk with different fat content.

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El-Mageed, Magda A. Abd

1997-12-01

Full Text Available Buffaloe's milk was manufactured to Domiati cheese with different fat content in the cheese milk (1%, 3.5% and 7%. Results obtained during the ripening period revealed that the low fat cheese (Karish is not able to long period storage, while half cream cheese had a good quality and flavour along the ripening period. The full cream cheese did not exceed the first month of ripening, then it deteriorated. The main components found were acrolein (propenal, heptanal, acetone, butan-2 one, ethanol, butan-2 ol, 2-methylpropan- 1-ol, 3-methyl butan-1-ol, ethyl propionate, propyl propionate, pentane and octane. Methyl mercaptan, methyl thiopropionate, and dimethyl trisulfide together with propyl butyrate, were existed in the samples which are characterized as bad cheese samples. Most of the previous compounds were developed after 1 month of ripening period.

La leche de búfalo fue procesada para obtener queso Domiati con diferente contenido graso en la cuajada (1%, 3.5% y 7%. Los resultados obtenidos durante el período de maduración revelaron que el queso con bajo contenido en grasa (Karish no permite un largo período de almacenamiento, mientras que el queso con un contenido medio en grasa tuvo una buena calidad y flavor durante el período de maduración. El queso con alto contenido graso no duró más que el primer mes de maduración, deteriorándose posteriormente. Los principales componentes encontrados fueron acroleína (propenal, heptanal, acetona, butan-2-ona, etanol, butan-2-ol, 2- metil-propan-1-ol, 3 metil butan-1-ol, propionato de etilo, propionate de propilo, pentano y octano. Metil mercaptol, tiopropionato de metilo y trisulfuro de dimetilo Junto con butirato de propilo se encontraron en muestras que fueron caracterizadas como muestras de quesos malos. La mayoría de los compuestos anteriores se produjeron después de un mes de período de maduración.

Intramolecular interactions in a new tris-dithizonatocobalt(III) complex

International Nuclear Information System (INIS)

Eschwege, Karel G. von; As, Lydia van; Joubert, Chris C.; Swarts, Jannie C.; Aquino, Manuel A.S.; Cameron, T. Stanley

2013-01-01

Graphical abstract: Electrochemically Co(HDz) 3 (5), show three main ligand-based redox processes, two reductions and one oxidation. Ligand oxidations can be resolved into three components highlighting effective intramolecular interactions between molecular fragments; a spectroelectrochemical study of (5) highlighted spectroscopic changes during the six observed redox steps. - Highlights: • Comparative CV's of dithizone (1), PhHg(HDz) and new Co(HDz) 3 (5), is discussed. • One oxidation and two reductions per ligand and a Co III/II couple for (5) are observed. • Mono- and tris-coordinated PhHg(HDz) and (5) have stable metal thioether bonds. • Crystal structure details explain good resolution between ligand redox processes. • Spectro-electrochemistry of (5) highlights spectroscopic properties of redox products. - Abstract: The reactions between dithizone (H 2 Dz (1)) or potassium dithizonate (KHDz (3)), and [Co(H 2 O) 6 ] 2+ (6), in acetone or methanol to liberate tris-dithizonatocobalt(III), Co(HDz) 3 (5), are described. The structure of (5) was confirmed by single crystal X-ray analyses and shows bidentate coordination to Co III via S and N donor atoms for all three HDz − ligands. A comparative voltammetric and spectro-electrochemical study revealed that (1) can be oxidised in two one-electron transfer steps, to generate a disulphide first and then HDz + . In contrast, upon complexation with cobalt, the free mercaptan group of (1) becomes a stable “metal thioether”, Co-S-C, which effectively prevents disulphide formation in all three ligands of (5) upon electrochemical oxidation. As a result, each ligand of Co(HDz) 3 shows just one oxidation process. Intramolecular communication between ligands is evident because the three separate ligand-based oxidations are well resolved. Two irreversible ligand reduction steps, each consisting of three unresolved components related to each of the three ligands, were also observed. The Co II /Co III couple

A randomized double blind crossover placebo-controlled clinical trial to assess the effects of a mouthwash containing chlorine dioxide on oral malodor

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Yokoyama Sayaka

2008-12-01

Full Text Available Abstract Background Previous research has shown the oxidizing properties and microbiological efficacies of chlorine dioxide (ClO2, however, its clinical efficacies on oral malodor have been evaluated only with organoleptic measurements (OM or sulphide monitors. No clinical studies have investigated the inhibitory effects of ClO2 on volatile sulfur compounds (VSCs using gas chromatography (GC. The aim of this study was to assess the inhibitory effects of a mouthwash containing ClO2 on morning oral malodor using OM and GC. Methods A randomized, double blind, crossover, placebo-controlled clinical trial was conducted among 15 healthy male volunteers, who were divided into 2 groups. In the first test phase, the group 1 subjects (N = 8 were instructed to rinse with the experimental mouthwash containing ClO2, and those in group 2 (N = 7 to rinse with the placebo mouthwash without ClO2. In the second test, phase after a one week washout period, each group used the opposite mouthwash. Oral malodor was evaluated before rinsing, right after rinsing and every 30 minutes up to 4 hours with OM, and concentrations of hydrogen sulfide (H2S, methyl mercaptan (CH3SH and dimethyl sulfide ((CH32S, the main VSCs of human oral malodor, were evaluated with GC. Results The baseline oral condition in the subjects in the 2 groups did not differ significantly. The mouthwash containing ClO2 improved morning bad breath according to OM and reduced concentrations of H2S, CH3SH and (CH32S according to GC up to 4 hours after rinsing. OM scores with ClO2 were significantly lower than those without ClO2 at all examination times. Significant reductions in the concentrations of the three kinds of VSCs measured by GC were also evident at all examination times. The concentrations of the three gases with ClO2 were significantly lower than those without ClO2 at most examination times. Conclusion In this explorative study, ClO2 mouthwash was effective at reducing morning malodor for 4

Effects of a mouthwash with chlorine dioxide on oral malodor and salivary bacteria: a randomized placebo-controlled 7-day trial

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Ohnuki Mari

2010-02-01

Full Text Available Abstract Background Previous research has shown the oxidizing properties and microbiological efficacies of chlorine dioxide (ClO2. Its clinical efficacies on oral malodor have been evaluated and reported only in short duration trials, moreover, no clinical studies have investigated its microbiological efficacies on periodontal and malodorous bacteria. Thus, the aim of this study was to assess the inhibitory effects of a mouthwash containing ClO2 used for 7 days on morning oral malodor and on salivary periodontal and malodorous bacteria. Methods/Design A randomized, double blind, crossover, placebo-controlled trial was conducted among 15 healthy male volunteers, who were divided into 2 groups. Subjects were instructed to rinse with the experimental mouthwash containing ClO2 or the placebo mouthwash, without ClO2, twice per day for 7 days. After a one week washout period, each group then used the opposite mouthwash for 7 days. At baseline and after 7 days, oral malodor was evaluated with Organoleptic measurement (OM, and analyzed the concentrations of hydrogen sulfide (H2S, methyl mercaptan (CH3SH and dimethyl sulfide ((CH32S, the main VSCs of human oral malodor, were assessed by gas chromatography (GC. Clinical outcome variables included plaque and gingival indices, and tongue coating index. The samples of saliva were microbiologically investigated. Quantitative and qualitative analyses were performed using the polymerase chain reaction-Invader method. Results and Discussion The baseline oral condition in healthy subjects in the 2 groups did not differ significantly. After rinsing with the mouthwash containing ClO2 for 7 days, morning bad breath decreased as measured by the OM and reduced the concentrations of H2S, CH3SH and (CH32S measured by GC, were found. Moreover ClO2 mouthwash used over a 7-day period appeared effective in reducing plaque, tongue coating accumulation and the counts of Fusobacterium nucleatum in saliva. Future research is

Startup and long-term performance of biotrickling filters packed with polyurethane foam and poplar wood chips treating a mixture of ethylmercaptan, H2S, and NH3.

Science.gov (United States)

Hernández, J; Lafuente, J; Prado, O J; Gabriel, D

2013-04-01

Treatment of a mixture of NH3, H2S, and ethylmercaptan (EM) was investigated for more than 15 months in two biotrickling filters packed with poplar wood chips and polyurethane foam. Inlet loads ranging from 5 to 10 g N-NH3 m-3 hr-1, from 5 to 16 g S-H2S m-3 hr-1, and from 0 to 5 g EM m-3 hr-1 were applied. During startup, the biotrickling filter packed with polyurethane foam was re-inoculated due to reduced biomass retention as well as a stronger effect of nitrogen compounds inhibition compared with the biotrickling filter packed with poplar wood. Accurate pH control between 7 and 7.5 favored pollutants abatement. In the long run, complete NH3 removal in the gas phase was achieved in both reactors, while H2S removal efficiencies exceeded 90%. EM abatement was significantly different in both reactors. A systematically lower elimination capacity was found in the polyurethane foam bioreactor. N fractions in the liquid phase proved that high nitrification rates were reached throughout steady-state operation in both bioreactors. CO2 production showed the extent of the organic packing material degradation, which allowed estimating its service lifetime in around 2 years. In the long run, the bioreactor packed with the organic packing material had a lower stability. However, an economic analysis indicated that poplar wood chips are a competitive alternative to inorganic packing materials in biotrickling filters. We provide new insights in the use of organic packing materials in biotrickling filters for the treatment of H2S, NH3, and mercaptans and compare them with polyurethane foam, a packing commonly used in biotrickling filters. We found interesting features related with the startup of the reactors and parameterized both the performance under steady-state conditions and the influence of the gas contact time. We provide relevant conclusions in the profitability of organic packing materials under a biotrickling filter configuration, which is infrequent but proven reliable

Kashagan oil field development. Kazakhstan

International Nuclear Information System (INIS)

Urbaniak, D.; Gerebizza, E.; Wasse, G.; Kochladze, M.

2007-12-01

Based on our research and field investigations of the Kashagan oil field development and relevant infrastructure in the Atyrau and Mangistau regions of Kazakhstan (cities and vicinities of Aktau, Atash, Atyrau, Bautino, Bolashak, Karabatan and Koshanai) evidence has been collected that raises serious concerns about environmental, social and health effects of this oil field development - such as sulphur emissions and storage which may pose serious threats for the communities close to the Kashagan oil facilities and for the Caspian Sea environment. Furthermore, since becoming the single Operator of the North Caspian Sea Production Sharing Agreement (PSA), the Agip Kazakhstan North Caspian Operating Company N.V. (Agip KCO) has failed to release all information available on the environmental, health and social impacts of its operations in the Kashagan oil field. As requested by the local communities and required by Constitution of Kazakhstan Republic and Aarhus Convention on Access to Information, Public Participation in Decision-Making and Access to Justice in Environmental Matters ratified by Kazakhstan in 2001, such information must be made available. There is also a growing concern among the civil society that the European Commission through its officials is publicly expressing support to European oil companies' members of the Agip KCO despite their failure to fulfil basic environmental regulations. This continued support contradicts the European Union's fundamental values and frequent statements related to Human Rights and Sustainable Development. Thousands of people have already been relocated in the region because of sulphur emissions and other highly poisonous chemicals such as mercaptans, which are present at very high levels in Northern Caspian oil. Unprotected storage of large quantities of sulphur is also recognised as a major cause of acid rain on a global level. This Report implores Agip KCO to release all available and required information on the

Methane-free biogas for direct feeding of solid oxide fuel cells

Science.gov (United States)

Leone, P.; Lanzini, A.; Santarelli, M.; Calì, M.; Sagnelli, F.; Boulanger, A.; Scaletta, A.; Zitella, P.

This paper deals with the experimental analysis of the performance and degradation issues of a Ni-based anode-supported solid oxide fuel cell fed by a methane-free biogas from dark-anaerobic digestion of wastes by pastry and fruit shops. The biogas is produced by means of an innovative process where the biomass is fermented with a pre-treated bacteria inoculum (Clostridia) able to completely inhibit the methanization step during the fermentation process and to produce a H 2/CO 2 mixture instead of conventional CH 4/CO 2 anaerobic digested gas (bio-methane). The proposed biogas production route leads to a biogas composition which avoids the need of introducing a reformer agent into or before the SOFC anode in order to reformate it. In order to analyse the complete behaviour of a SOFC with the bio-hydrogen fuel, an experimental session with several H 2/CO 2 synthetic mixtures was performed on an anode-supported solid oxide fuel cell with a Ni-based anode. It was found that side reactions occur with such mixtures in the typical thermodynamic conditions of SOFCs (650-800 °C), which have an effect especially at high currents, due to the shift to a mixture consisting of hydrogen, carbon monoxide, carbon dioxide and water. However, cells operated with acceptable performance and carbon deposits (typical of a traditional hydrocarbon-containing biogas) were avoided after 50 h of cell operation even at 650 °C. Experiments were also performed with traditional bio-methane from anaerobic digestion with 60/40 vol% of composition. It was found that the cell performance dropped after few hours of operation due to the formation of carbon deposits. A short-term test with the real as-produced biogas was also successfully performed. The cell showed an acceptable power output (at 800 °C, 0.35 W cm -2 with biogas, versus 0.55 W cm -2 with H 2) although a huge quantity of sulphur was present in the feeding fuel (hydrogen sulphide at 103 ppm and mercaptans up to 10 ppm). Therefore, it

Methane-free biogas for direct feeding of solid oxide fuel cells

Energy Technology Data Exchange (ETDEWEB)

Leone, P.; Lanzini, A.; Santarelli, M.; Cali, M. [Dipartimento di Energetica, Politecnico di Torino, Corso Duca degli Abruzzi 24, 10129 Turin (Italy); Sagnelli, F.; Boulanger, A.; Scaletta, A.; Zitella, P. [BioEnergy Lab, Environment Park S.p.A., Via Livorno 60, 10144 Turin (Italy)

2010-01-01

mercaptans up to 10 ppm). Therefore, it was demonstrated the interest relying on a sustainable biomass processing which produces a biogas which can be directly fed to SOFC using traditional anode materials and avoiding the reformer component since the methane-free mixture is already safe for carbon deposition. (author)

Use of multi-objective air pollution monitoring sites and online air pollution monitoring system for total health risk assessment in Hyderabad, India.

Science.gov (United States)

Anjaneyulu, Y; Jayakumar, I; Hima Bindu, V; Sagareswar, G; Mukunda Rao, P V; Rambabu, N; Ramani, K V

2005-08-01

electrochemical sensor systems (sulphur dioxide, oxides of nitrogen, carbon monoxide, hydrocarbons, ozone, mercaptans and hydrogen sulphide) and a particulate matter analyzer (total suspended particulate matter TSPM), PM2.5 and PM10). The sensor and data acquisition systems are programmed to monitor pollution levels at 1/2 hour durations during peak hours and at 1-hour intervals at other times. Presently, extensive statistical and numerical simulations are being carried out at our center to correlate the individuals living in the monitored areas with respiratory infections with air pollution.

Use of Multi-Objective Air Pollution Monitoring Sites and Online Air Pollution Monitoring System for Total Health Risk Assessment in Hyderabad, India

Directory of Open Access Journals (Sweden)

K. V. Ramani

2005-08-01

-time monitoring system was designed using advanced electrochemical sensor systems (sulphur dioxide, oxides of nitrogen, carbon monoxide, hydrocarbons, ozone, mercaptans and hydrogen sulphide and a particulate matter analyzer (total suspended particulate matter TSPM, PM2.5 and PM10. The sensor and data acquisition systems are programmed to monitor pollution levels at ½ hour durations during peak hours and at 1-hour intervals at other times. Presently, extensive statistical and numerical simulations are being carried out at our center to correlate the individuals living in the monitored areas with respiratory infections with air pollution.

Modern view on hepatic encephalopathy: basic terms and concepts of pathogenesis

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T. V. Shulyatnikova

2017-12-01

Full Text Available Background. The problem of acute and chronic forms of hepatic encephalopathy (HE is not clearly identified among modern problems of hepatology and neuroscience in Ukraine. Despite the significant contribution to the development of lethal complications in patients with liver pathology and long history of the study of this issue, there is still no unified opinion on the links of HE pathogenesis. The aim of this review is to conduct a comprehensive analysis of current data on the spreading and mechanisms of development of HE. HE is a complex of potentially reversible neurocognitive disorders in patients with chronic or acute hepatic failure (ALF. HE is more often a complication of liver cirrhosis and is the second most frequent cause of hospitalization of such patients after ascites. When decompensating liver failure in acute or chronic hepatic pathology in patients severe forms of HE develop, accompanied by a progressive increase in intracranial pressure and the development of coma, which often ends lethal due to poor corrigibility of intracranial hypertension while maintaining hepatogenic neurointoxication. HE is considered as the end result of the accumulation of a number of neurotoxic substances in the brain, among which are ammonia, mercaptans, short chain fatty acids, false neurotransmitters, gamma-aminobutyric acid, manganese. The most popular among the reasons for the development of HE is the neurotoxic theory of ammonia. Ammonia is subjected to detoxification in the liver, turning into urea, a smaller fraction with the participation of glutamine synthetase is used in the synthesis of glutamine in muscles, liver and astrocytes of brain. In case of hepatic dysfunction and/or portosystemic shunting, the concentration of ammonia in blood increases up to 10 times and the main load for its detoxification is shifted to myocytes and astroglia. In ALF glutamine overload of astrocytes occurs with a change in intracellular osmolarity and subsequent

Nuisance Odors: Is there a Concern - 12340

Energy Technology Data Exchange (ETDEWEB)

Brounstein, Robert A. [TerranearPMC, Los Alamos New Mexico 87544 (United States)

2012-07-01

Nuisance odors are generally thought of as just being annoying or unpleasant and not causing any physiological harm to our internal organs or other biologic systems. Yet during an excavation of buried animal remains, field workers experienced a multitude of symptoms that are associated with exposures to toxic materials. An examination of the decomposition process revealed that there is a potential off-gassing of a number of common, yet harmful chemicals including ammonia, mercaptans, hydrogen sulfide, butyric acid and phenol. In addition, other compounds, that have limited information such as established health data and occupational exposure limits, were also potential contaminants-of-concern. While a variety of monitoring and sampling techniques were used to assess worker exposures, all results indicated non-detectable airborne concentrations. Nevertheless, workers were experiencing such symptoms as nausea and headaches. As such, protective measures were necessary for field personnel to continue work while having confidence that the project was instituting sincere steps to ensure their health and safety. Researching the possible reasons for the causes of workers exhibiting adverse health effects from nuisance odors revealed that such exposures initiate electrochemical pathways, starting from the olfactory bulb to the brain, followed by a transfer of information to such biologic systems as the hypothalamus and pituitary gland. These systems, in turn, secrete hormones that cause a number of involuntary reactions; many of which are observed as typical adverse health effects, when in fact, they are merely reactions caused by the brain's memory; most likely created from previous experiences to unpleasant odors. The concern then focuses of how the Occupational Safety and Health community shall respond to such workplace exposures. Future work in this area may need to focus on the viability of current occupational exposure limits and the possibility of revising these

Final Report, Materials for Industrial Heat Recovery Systems, Tasks 3 and 4 Materials for Heat Recovery in Recovery Boilers

Energy Technology Data Exchange (ETDEWEB)

Keiser, James R.; Kish, Joseph R.; Singh, Preet M.; Sarma, Gorti B.; Yuan, Jerry; Gorog, J. Peter; Frederick, Laurie A.; Jette, Francois R.; Meisner, Roberta A.; Singbeil, Douglas L.

2007-12-31

tubes. Also, these fluctuating air flow patterns can result in deposition of black liquor on the wall tubes, and during periods when deposition is high, there is a noticeable increase in the concentrations of sulfur-bearing gases like hydrogen sulfide and methyl mercaptan. Laboratory studies have shown that chromized and aluminized surface treatments on carbon steel improve the resistance to sulfidation attack. Studies of superheater corrosion and cracking have included laboratory analyses of cracked tubes, laboratory corrosion studies designed to simulate the superheater environment and field tests to study the movement of superheater tubes and to expose a corrosion probe to assess the corrosion behavior of alternate superheater alloys, particularly alloys that would be used for superheaters operating at higher temperatures and higher pressures than most current boilers. In the laboratory corrosion studies, samples of six alternate materials were immersed in an aggressive, low melting point salt mixture and exposed for times up to 336 h, at temperatures of 510, 530 or 560°C in an inert or reactive cover gas. Using weight change and results of metallographic examination, the samples were graded on their resistance to the various environments. For the superheater corrosion probe studies, samples of the same six materials were exposed on an air-cooled corrosion probe exposed in the superheater section of a recovery boiler for 1000 h. Post exposure examination showed cracking and/or subsurface attack in the samples exposed at the higher temperatures with the attack being more severe for samples 13 exposed above the first melting temperature of the deposits that collected on the superheater tubes. From these superheater studies, a ranking was developed for the six materials tested. The task addressing cracking and corrosion of primary air port tubes that was part of this project produced results that have been extensively implemented in recovery boilers in North America

Isotopic data to study the mechanism of the oxidation of mercaptoacetic acid; Donnees isotopiques pour l'etude du mecanisme d'oxydation de l'acide mercaptoacetique; Izotopnyj metod issledovaniya mekhanizma okisleniya merkapgouksusnoj kisloty; Estudio del mecanismo de oxidacion del acido mercaptoacetico por medio de datos obtenidos con radioisotopos

Energy Technology Data Exchange (ETDEWEB)

Gal, D [Central Isotope Laboratory, University of Szeged (Hungary); Guczi, L [Department of Radiology, Elelmiszeripari Kutato Intezet, Budapest (Hungary)

1962-03-15

Numerous researchers have been studying the liquid-phase autoxidation by molecular oxygen of compounds containing a mercapto group. It has been stated that, in the course of the reaction, sulphide is formed, but the exact mechanism of this process has not been determined. The oxidation of mercaptoacetic acid, at 50{sup o}C and at a pH of 8, was investigated both in the presence of Complexon IV and in the presence of iron-ions. Na{sub 2}S, labelled with S{sup 35}, was introduced into the system and it was determined that this sulphide considerably increases the rate of the oxygen uptake both in the processes catalysed by trivalent iron and free of iron-ions. In the course of the reaction the concentration of the sulphide, its specific activity and its total activity were measured. In using these data and on the basis of the kinetic isotopic method developed by Neiman and co-workers, it was possible to calculate the rate of sulphide formation and its further oxidation. In comparing these data with other kinetic data, it is shown that the oxidation of mercaptoacetic acid in the liquid phase is a branching chain reaction; one of its principal chains being the formation of Na{sub 2}S and its further oxidation. Moreover, it was determined that sulphate is formed in the course of the reaction only through the inorganic sulphide. Iron-ions catalyse the formation of organic disulphide and therefore also have influence on the sulphide formation. (author) [French] De nombreux chercheurs ont etudie l'autoxydation des composes contenant un groupe mercaptan par l'oxygene moleculaire en phase liquide. Ils ont trouve qu'il y avait formation de sulfure au cours de la reaction, mais le mecanisme exact de ce processus n'a pas ete determine. L'oxydation de l'acide mercaptoacetique a 50{sup o}C et pour un pH de 8 a ete etudiee en presence de complexone IV et egalement; en presence de fer. Du Na{sub 2}S marque au {sup 35}S a ete introduit dans le systeme et on a constate que le Na{sub 2