• 동아시아식생활학회지
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• 제3권2호
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• pp.121-128
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• 1993

This study was intended to clarify the protective mechanism of diallyl disulfide on the carbon tetrachloride-induced hepatotoxicity in mice. It was observed that a powerfully increment of serum alanine aminotransferase activity and hepatic lipid peroxide content after carbon tetrachloride injection were markedly inhibited by the pretreatment of diallyl disulfide (20mg/kg) for 5 days. It was also observed that hepatic aminopyrine demethylase and xanthine ocidase as free radical generating enzymes as well as superoxide dismutase and catalase activities as free frdical scavenging enzymes and hepatic glutathione content were not changed by the pretreatment with diallyl disulfide. But, treatment with diallyl disulfide did signifiantly increase cytosolic glutathione S-transferase activity. However, glutathione S-transferase activity in the presence of diallyl disulfide was not affected in vitro. Therefore, it is concluded that mechanism for the observed preventive effect ofdiallyl disulfide against the carbon tetrachloride-induced hepatotoxicity can be due to the engancement of glutathione S-transferase activity.

• 농촌의학ㆍ지역보건
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• 제41권2호
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• pp.63-74
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• 2016

Objectives: We surveyed the awareness and current status of using fumigant carbon disulfide for exterminate Curculio sikkimensis among chestnut farmers in Chungnam Province to suggest directions for health education and public relations. Methods: We designed questionnaires to evaluate recognition of fumigant carbon disulfide. We conducted a questionnaire survey to assess recognition and recognition level of fumigant carbon disulfide by the study variables. Results: The recognition status for fumigant carbon disulfide was 74.5%, but the recognition level was low (know well 27.5%). The path of recognition was 45.1% and 15.7% for neighbor and rural technology center, respectively. The recognition status for warning label of fumigant carbon disulfide was 52.9%. Recognition for warning label of fumigant carbon disulfide was tended to increase with high educational attainment, bigger owning land area. Recognition on the content of warning label were 29.4%, 27.5%, 21.6%, and 21.6% for inflammability, toxicity, hazard, and explosiveness, respectively. Using personal protection equipment was tended to increase with the high status of awareness on fumigant carbon disulfide. Conclusions: Health education programs for using fumigant carbon disulfide are needed for chestnut farmers. In addition, publicity information activities about prevention and protection of carbon disulfide poisoning are needed for high risk farmers.

• 한국산업보건학회지
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• 제6권2호
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• pp.202-208
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• 1996

The purposes of this study are the identification and determination of metabolites in the isolated rat liver perfusate of carbon disulfide by two-dimentional thin-layer chromatography and high performance liquid chromatography for understanding the metabolism of carbon disulfide. 2-Thio-thiazolidine-4-carboxylic acid(TTCA) was synthesized by the reaction of carbon disulfide and cysteine, and confirmed by two-dimentional thin-layer chromatography, high performance liquid chromatography, UV spectroscopy, and IR spectroscopy. The absorbance of UV detector for the simultaneous determination of TTCA and thiocarbamide was 254 nm although their maximum spectra were 273 nm and 237 nm, respectively. Two kinds of the developing solvent in the two-dimentional thin-layer chromatography were 2-butanol : 80% HCOOH : $H_2O$ (7 : 2 : 1) as the first developing solvent and 2-propanol : $H_2O$ (4 : 1) as the second developing solvent. After perfusion of carbon disulfide ($8274.23{\mu}mol$), the amount of TTCA and thiocabamide of the perfusate(100 ul) were $12.02-16.4{\mu}mol$ and $5.25-8.15{\mu}g$, respectively. The mean amount of them were $14.08{\mu}mol$ and $6.41{\mu}mol$ respectively, and the former was 2.20 times greater than the latter. For conforming the mechanism of formations of TTCA and thiocarbamide in vivo, we have to clarify whether the reactions between carbon disulfide and ammonia, ammonium salts, amides, cysteine, cystine, or proteins will be formed in vitro.

• International Journal of Automotive Technology
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• 제7권4호
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• pp.501-508
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• 2006

The effect of chemical additives, such as dimethyl ether(DME), ethanol, carbon disulfide on the soot formation were examined numerically. ill this study, the Frenklach soot mechanism was used as a base mechanism to predict the soot formation in the ethane flame. The combination of Westbrook's DME mechanism, Marinov's ethanol mechanism, and chemical kinetic mechanism for hydrogen sulfide and carbon disulfide flames was made with the base mechanism because the DME, ethanol, $CS_2$ additives are added into the ethane fuel. CHEMKIN code was used as a numerical analysis software to simulate the effect of chemical additives on reduction of the polycyclic aromatic hydrocarbons(PAH's) which are soot precursors. From the numerical results it is observed that addition of DME, ethanol and $CS_2$ into ethane fuel can reduce PAH species significantly. That means theses additives can reduce soot formation significantly. Results also strongly suggest suppression of soot formation by these additives to be mainly a chemical effect. Hand OH radicals may be the key species to the reduction of PAH species for additives.

• 월간산업보건
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• 통권326호
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• pp.47-50
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• 2015

• 분석과학
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• 제26권6호
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• pp.381-386
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• 2013

본 연구는 유해화학물질관리법에 지정되어 있는 사고대비물질 중 휘발성과 화재위험성 등급이 높은 알릴클로라이드(allyl chloride, AC)와 이황화탄소(carbon disulfide, CD)에 대하여 테들라 백에서의 보존 특성을 연구하였다. 테들라 백에서의 시료 보존성을 연구하기 위하여 시료 보존성에 영향을 줄 수 있는 시료보관 온도($2^{\circ}C$, $25^{\circ}C$), 물질 농도(저농도, 고농도), 보관 시간(0시간, 48시간, 96시간, 144시간), 단일물질과 혼합물질 등의 영향인자를 비교하여 연구하였다. 테들라 백 내에서의 시료 보존율은 시간 경과에 따라 감소하였고 각 영향인자에 대한 T-검정결과 농도와 혼합형태에 따라 유의한 차이를 보였다. 본 연구결과는 테들라 백을 사용하여 시료 채취 시 대상물질에 대한 정량적 분석정보를 제공하는데 도움이 될 것으로 판단된다.

• 한국식품영양과학회지
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• 제37권10호
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• pp.1330-1336
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• 2008

본 연구는 고품질의 동치미 제조를 위해 고온살균에서 발생될 수 있는 향기 성분의 변화와 영양소 파괴 등으로 인한 품질저하의 문제점을 해결하기 위해 비열처리 공정인 초임계 이산화탄소를 이용하였으며 이화학적 품질특성을 조사하였다. 그 결과 pH, 산도 및 색도는 상압에서 가열처리한 동치미와 초임계 이산화탄소를 처리한 동치미 모두 뚜렷한 변화를 나타내지 않았으며 비타민 C의 경우 초임계 이산화탄소 처리구가 상압에서 가열처리한 구간보다 더욱 안정함을 보였다. 유기산과 유리당의 경우는 초임계 이산화탄소 처리구가 상압에서 가열처리한 구간보다 다소 낮은 함량을 보였으나 그 차이는 매우 적음을 알 수 있었다. 휘발성 향기 성분은 dimethyl disulfide, methyl trisulfide, methyl propyl disulfide 등 마늘과 파 등의 특유의 강한 향기성분들은 초임계 이산화탄소처리에 의해 대부분 감소됨을 보여주었다. 초임계 이산화탄소를 이용하여 동치미 무의 polygalacturonase 효소를 불활성화 시키기 위해서는 25 MPa 이상의 압력과 $55^{\circ}C$ 이상의 온도가 요구됨을 확인하였다. 따라서 동치미의 살균을 위해 초임계 이산화탄소를 처리함으로써 동치미 중 PGase 효소의 불활성화가 가능하며, 산업적 응용을 위해서는 무를 제외하고 동치미 액만을 활용하는 것이 용이하다 사료된다.

• 공업화학
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• 제1권2호
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• pp.176-181
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• 1990

탄소섬유/알루미늄 복합 재료의 계면 전단 강도를 향상시키기 위하여 탄소섬유 표면을 $400-600^{\circ}C$의 온도 범위에서 황화수소 기체로 처리하였다. 처리 탄소섬유 표면의 변화를 주사 전자 현미경과 X-선 광전자 스펙트럼에 의해 관찰하고 분석하여 표면 처리 탄소섬유의 표면에 황 화합물이 존재하는 것을 확인하고, 표면처리 탄소섬유의 탄소 및 탄소의 함량 변화를 조사하였다. 탄소섬유 표면의 황화수소 기체 처리의 최적 온도는 $550^{\circ}C$였고, 처리 탄소섬유 표면의 황 화합물은 disulfide, $(S)_n$ 및 thiophene의 형태를 이루고 있었다. 처리 탄소섬유는 처리 온도 $400-600^{\circ}C$의 범위에서 5% 정도의 인장 강도 저하를 나타냈다.

• Bulletin of the Korean Chemical Society
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• 제29권1호
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• pp.51-56
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• 2008

The regioselective ring opening of epoxides using elemental iodine and bromine in the presence of methimazole (MMI, a anti-thyroid drug) and its metabolite methimazole-disulfide as new catalysts are studied. MMI easily converted in vitro to MMI-disulfide without any double activation presented in vivo. FT-Raman and UV spectroscopies are used to study the interaction of iodine with these catalysts. The results indicate that both catalysts are efficient in polyiodide formation, but MMI-disulfide can catalyze this reaction in higher yield and regioselectivity. The complex [(MMI-disulfide)I]+.I3- is considered to be formed initially which could be bulkier by addition of excess of iodine in the course of the reaction. These bulky nucleophiles have a fundamental role in the high regioselectivity by attacking the less sterically hindered epoxide carbon. In this study we suggest that MMI is readily converted to MMI-disulfide by interaction with iodine or activated iodine in thyroid gland, and this process is responsible for high anti-thyroid activity of MMI.

• Bulletin of the Korean Chemical Society
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• 제19권11호
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• pp.1262-1265
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• 1998