• 제목/요약/키워드: sulfur chemistry

검색결과 360건 처리시간 0.033초

잠재 산성황산염토양의 산화과정에 대한 연구 (Study on the Oxidation Process of Potential Acid Sulfate Soil)

  • 한강완;전재철;조재영;김금희;안열
    • 한국토양비료학회지
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    • 제29권3호
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    • pp.243-248
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    • 1996
  • 잠재 산성황산염토양의 산화과정과 이 토양에서 유래된 잠재 산성황산염토양을 칼럼에 넣고 개량제 시용에 따른 토양특성의 변화에 대한 연구결과는 다음과 같다. 1. 잠재 산성황산염토양의 건조와 담수 조건에서 토양 pH변화는 시간의 경과에 따라 두 조건 모두 낮아지는 경향을 나타내었는데 그 낮아지는 폭이 건조조건에서 더 크게 나타났다. 2. Sulfate-sulfur의 함량은 건조조건에서 증가하였으나 담수상태에서는 점점 감소하는 경향이었으며 sulfide-sulfur의 함량은 담수조건이 더 높게 나타났다. 3. 2가 철의 함량은 시간의 지남에 따라 담수조건에서 함량이 더 높았고 건조조건에서는 서서이 감소하는 경향이었으며 치환성 알루미늄의 함량은 건조와 담수 두 조건에서 모두 증가하였다. 4. 컬럼을 이용한 모델실험에서 잠재 산성황산염토양에 농용석회, 암모니아수를 처리하여 중화시킨 후시간이 경과됨에 따라 대조구에 비하여 pH가 상승하였지만 그 효과가 크게 나타나지는 않았다. $Eh_6$는 암모니아수 처리가 제일 낮았으며 다음이 농용석회, 대조구의 순서였다. 5. 칼럼용출액 중의 sulfate-sulfur와 치환성 알루미늄의 함량은 시간이 경과함에 따라 모든 처리구에서 감소하는 경향이었고, sulfide-sulfur와 2가 철의 함량은 증가하는 경향이었다.

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혐기성 소화 가스로부터 황화합물의 제거 (Removal of Sulfur Compounds from Anaerobic Digestion Gas)

  • 최도영;장성철;안병성;최대기
    • 공업화학
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    • 제19권1호
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    • pp.31-36
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    • 2008
  • 혐기성소화가스(ADG)를 원료로 수소를 제조하여 연료전지에 활용할 경우 ADG에 포함된 황화합물이 개질기의 촉매와 연료전지의 전극에 독으로 작용하므로 금속이온이 담지된 활성탄을 이용하여 황화합물을 제거하였다. 수분과 산소농도에 따라 고정층 흡착량이 변화하였으며, 산소 0.2 vol%, RH 90% 이상일 때 가장 높은 흡착량을 나타내었다. 본 연구에서는 KI 첨착한 활성탄에서 황화합물의 흡착특성을 고정층에서 동특성 실험을 통해 관찰하고 그 결과를 기준으로 흡착탑을 설계 제작 현장실험을 실시하였다.

Kinetics Studies on the Mechanism of Hydrolysis of S-Phenyl-S-vinyl-N-p-tosylsulfilimine Derivatives

  • Pyun, Sang-Yong;Kim, Tae-Rin;Lee, Chong-Ryoul;Kim, Whan-Gi
    • Bulletin of the Korean Chemical Society
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    • 제24권3호
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    • pp.306-310
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    • 2003
  • Hydrolysis reactions of S-phenyl-S-vinyl-N-p-tosylsulfilimine (VSI) and its derivatives at various pH have been investigated kinetically. The hydrolysis reactions produced phenylvinylsulfoxide and p-toluene sulfonamide as the products. The reactions are first order and Hammett ρ values for pH 1.0, 6.0, and 11.0 are 0.82, 0.45, and 0.57, respectively. This reaction is not catalyzed by general base. The plot of k vs pH shows that there are three different regions of the rate constants $(k_t)$ in the profile.; At pH < 2 and pH > 10, the rate constants are directly proportional to the concentrations of hydronium and hydroxide ion catalyzed reactions, respectively. The rate constant remains nearly the same at 2 < pH < 10. On the bases of these results, the plausible hydrolysis mechanism and a rate equation have been proposed: At pH < 2.0, the reaction proceeds via the addition of water molecule to sulfur after protonation at the nitrogen atom of the sulfilimine, whereas at pH > 10.0, the reaction proceeds by the addition of hydroxide ion to sulfur directly. In the range of pH 2.0-10.0, the addition of water to sulfur of sulfilimine appears to be the rate controlling step.

일정전류 비평행교류브릿지에 의한 전도도측정과 황의 정량 (An Unbalanced A.C. Bridge with High Voltage Source for the Conductometric Determination of Sulfur in Iron Ores)

  • 채명준;최규원
    • 대한화학회지
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    • 제14권4호
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    • pp.327-332
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    • 1970
  • A simple and convenient device for deflection-type direct reading the variations in electrolytic conductance is described and applied to the analysis of sulfur by combustion-$H_2O_2$ oxidation method. The apparatus consisted of a high resistance-ratio bridge in which the other adjacent arms are the differential cells. By adopting unusually high a-c voltage source for the bridge excitation, the a-c method for unbalanced bridge is established, decreased sensitivity owing to reduced bridge factor, 0.01, is overcome and also the absolute sensitivity and linearity are greatly improved. Over 50% variations in impedance of the balanced cell, within 1% deviation from the linearity can be attained with a volt (rms)order of output which was detected directly with VTVM without further amplification. Analysis of the bridge shows that these useful features are natural result of the constant current character of the high source impedance generator and the performance of the device agreed with the theoretical predictions. A standard procedure for the rapid analysis of sulfur using the bridge is also given, the analytical accuracy was approximately 1%. A determination takes not more than 5 minutes.

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Pyrolysis-Gas Chromatography를 이용한 가황 고무의 열분석에 관한 연구(II) (NBR, CR 및 EPDM 가황체) (Studies on analysis of Rubber Vulcanizates by Pyrolysis-Gas Chromatography (II) (NBR, CR, and EPDM Vulcanizates))

  • 허동섭;김종석;김경자;안병국;서수교
    • Elastomers and Composites
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    • 제22권4호
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    • pp.314-323
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    • 1987
  • A blend ratio of rubber vulcanzates comprising NBR, CR, EPDM, NR, BR, and SBR alone or blended is determind through a P.G.C. It is found that a characteristic peak of elastomer is proportional to the content of each elastomer when they are pyrolysed. It is also classified to the different AN content in NBR vulcanizates, identification of sulfur-modified and non-sulfur bearing CR polymers, and the content of ethylene, propylene monomer and the third monomer in EPDM vulcanizetes.

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Chemistry of Carbonate-Sulfur Flux

  • Q. Won Choi;Choi Han;Chang So-Young;Pyun Chong-Hong;Kim Chang-Hong
    • Bulletin of the Korean Chemical Society
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    • 제15권12호
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    • pp.1118-1121
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    • 1994
  • Reactions of alkaline metal carbonates with sulfur are investigated in detail. The evolution of CO and a trace of $SO_2$ were observed in the course of reaction with major component of polysulfides. Some evidences that the reaction proceeds with breaking of terminal sulfur-sulfur bond in the sulfur polymer, and forming CO, $SO_2$ and polysulfide are presented. Polysulfides have the role of keeping free sulfur and allow it to react with other chemicals to rather high temperatures.plexes, whereas the binuclear and mononuclear complexes of Mn$^{2+}$ and Co$^{2+}$

Iodine-Sulfur 수소 제조 공정에서 $H_2SO_4-HI-H_2O-I_2$ 계의 고온 상 분리 (High Temperature Phase Separation of $H_2SO_4-HI-H_2O-I_2$ System In Iodine-Sulfur Hydrogen Production Process)

  • 이동희;이광진;강영한;김영호;박주식;황갑진;배기광
    • 한국수소및신에너지학회논문집
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    • 제17권4호
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    • pp.395-402
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    • 2006
  • Iodine-sulfur(IS) hydrogenation production process consists of three sections, which are so called a Bunsen reaction section, a HI decomposition section and a $H_2SO_4$ decomposition section as a closed cycle. For highly efficient operation of a Bunsen reaction section, we investigated the phase separation characteristics of $H_2SO_4-HI-H_2O-I_2$ system into two liquid phases($H_2SO_4$-rich phase and $HI_x$-rich phase) in the high temperature ranges, mainly from 353 to 393 K, and in the $H_2SO_4/HI/H_2O/I_2$ molar ratio of $1/2/14{\sim}30/0.3{\sim}13.50$. The desired results for the minimization of impurities in each phase were obtained in conditions with the higher temperature and the higher $I_2$ molar composition. On the basis of the distribution of $H_2O$ to each phase, it is appeared that the affinity between $HI_x$ and $H_2O$ was more superior to that between $H_2SO_4$ and $H_2O$.

INVESTIGATIONS ON VARIABLE WELD PENETRATIONS IN GTA WELDING OF AUSTENITIC AND MARTENSITIC STAINLESS STEELS

  • Puybouffat, Sylvain;Chabenat, Alain;Boudot, Cecile;Marya, Surendar
    • 대한용접접합학회:학술대회논문집
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    • 대한용접접합학회 2002년도 Proceedings of the International Welding/Joining Conference-Korea
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    • pp.752-756
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    • 2002
  • Variable weld bead penetrations related to the base metal chemistry of stainless steels in GTA welding have been under constant investigations due to their industrial implications. It has been proposed that among other elements, the sulfur content of steels determines the weld pool geometry, particularly its penetration. It is suggested that the surface tension temperature gradient of steels becomes positive with appropriate dosing in sulfur and results in inward melt flow, propitious for deeper welds. However, the chemistry of industrial steels is complex due to the presence of multiple minor elements either deliberately added or remnant impurity traces. With this in view, investigations on 41 austenitic and nine martensitic stainless steels were carried to see if there existed any possible relation between the weld profile and some of the designated elements. The results suggest no direct correlation between sulfur or any other major or trace element and weld penetration. At first glance the results are contradictory to what is often asserted.

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Novel Linking Ligand Containing Sulfur-Donor Atoms and Its Compounds of Palladium and Silver

  • Lee, Hee-K.;Lee, Soon-W.
    • Bulletin of the Korean Chemical Society
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    • 제28권3호
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    • pp.421-426
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    • 2007
  • A linking ligand containing sulfur donor atoms in the terminal thiophene rings, 1,2-bis(thiophen-2-ylmethylene) hydrazine (L), was prepared by Schiff-base condensation. Ligand L reacted with [PdCl2(NCPh)2] to produce a molecular Pd compound [PdL2Cl2] (1). On the other hand, it reacted with AgNO3 and AgClO4 to produce a 2-D network [AgL0.5(NO3)] (2) and a 1-D polymer [AgL]ClO4 (3), respectively, whose structures are based on secondary intermolecular forces such as H-bonding, van der Waals interaction, and π-π stacking. Polymer 2 exhibited photoluminescence at room temperature in the solid state.