• Title/Summary/Keyword: Thiourea

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Sequential Oxidative and Reductive Bleaching of MOW by the Addition of Thiourea (Thiourea 첨가에 의한 MOW의 산화-환원 연속 표백)

  • 김승호;안병준;백기현
    • Journal of Korea Technical Association of The Pulp and Paper Industry
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    • v.34 no.3
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    • pp.38-45
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    • 2002
  • The effect of sequential oxidative-reductive bleaching on brightening of the MOWs is investigated. The improvement in brightnesses of MOWs is more effective in conventional PFAS bleaching than in P/T bleaching. There is no difference in the mechanical properties or the bleached pulps between PFAS and P/T sequences. Considering the brightness gains and bleaching chemicals cost, for the MOW A(Initial brightness: 68.3% ISO) containing 5% ONP and 20% colored paper, the P/T bleaching is more economical than the PFAS bleaching. However for MOW B(initial brightness: 59.1% ISO) containing 15% ONP and 35% colored paper, there is no difference in the bleaching efficiency between PFAS and P/T bleaching.

Effects of Stabilizing Additives on Electroless Copper Deposition (무전해 동 도금용액 속에서 안정제의 역할)

  • 최순돈;박범동
    • Journal of the Korean institute of surface engineering
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    • v.25 no.4
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    • pp.173-180
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    • 1992
  • The effects of the stabilizing additives such as NaCN, 2-MBT and Thiourea on bath decom-position, plating rate and surface morphology have been studied. Bath stability was increased in the order of an additive-free bath, and NaCN-, 2-MBT-, and Thiourea-stabilized baths. The sta-bilizing effects may be attributed to the stability of Cu(II) -complexes. The plating rate is the re-verse order of the bath stability. Accelerative effect of 2-MBT in proper quantity(0.3mg/$\ell$) may be explained by visualizing it absorbed through benzene ring or sulfur atom on portions of the sub-strates. The strong bond of the complexing part of the molecule to nearby chelated copper ions would tend to accelerate plating by making it easier for the Cu2+ -ligand bond to be broken. Sur-face morphologies of copper deposits depend on the bath additives. Electroless copper deposits from the 2-MBT stabilized baths are finer than the deposits from the NaCN- and Thiourea- stabi-lized baths due to the strong adsorption on the substrates.

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High-speed Gold Electrowinning from Thiourea Solution (Thiourea 용액으로부터 금의 고속 전해채취)

  • Lee, Jong-Ho;Nam, Chul-Woo;Lee, Churl-Kyoung
    • Proceedings of the Korean Institute of Resources Recycling Conference
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    • 2003.10a
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    • pp.241-245
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    • 2003
  • Thiourea 용액에서 금의 고속 전해채취를 위해 사이클론 전해조를 사용하여 금의 회수에 대한 연구를 수행하였다. 금 전해채취의 전해거동을 알기 위해 전해질의 유속, 인가전압, 초기 농도 등의 변수에 대한 실험을 하였다. 기초실험을 통하여 얻은 최적조건 조업하에서 2시간 이내에 전해액 중에 존재하는 99%이상의 금을 회수할 수 있었다.

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Synthesis of Heterocycle-linked Thioureas and Their Inhibitory Activities of NO Production in LPS Activated Macrophages

  • Cheon, Ye-Jin;Gim, Hyo-Jin;Jang, Hee-Ryun;Ryu, Jae-Ha;Jeon, Raok
    • Bulletin of the Korean Chemical Society
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    • v.31 no.1
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    • pp.27-30
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    • 2010
  • A series of thioureas were synthesized as inhibitors of NO production in lipopolysaccharide-activated macrophages. We investigated the effect of lipophilic moiety and N-substituents of the thioureas on the activity. Phenoxazine and carbazole-containing derivatives revealed higher activity than indole-containing thioureas. The appropriate spacer between lipophilic tail and thiourea head and methyl substituent at N3 position of thiourea brought beneficial effect on the inhibition of NO production. Among prepared compounds, phenoxazine-containing derivative 2a was the most potent with $2.32 {\mu}M$ of $IC_{50}$ value. RT-PCR analysis suggested that the prepared thioureas inhibited NO production through the suppression of iNOS mRNA expression.

Synthesis of N,N',N"-Trisubstituted Thiourea Derivatives and their Antagonistic Effect on the Vanilloid Receptor

  • Park, Hyeung-Geun;Park, Mi-Kyung;Choi, Ji-Yeon;Choi, Sea-Hoon;Lee, Ji-Hye;Suh, Young-Ger;Cho, Ha-Won;Oh, Uh-Taek;Lee, Jee-Woo
    • Proceedings of the PSK Conference
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    • 2003.04a
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    • pp.253.1-253.1
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    • 2003
  • Twenty-seven N,N',N"-trisubstituted thiourea derivatives were prepared. Among them, 1- [3-(4'-hydroxy-3'-methoxy-phenyl)-propyl] -1,3-diphenethyl-thiourea (81, IC$\sub$50/= 0,32 $\mu\textrm{m}$), showed 2-fold higher antagonistic activity than that of capsazepine (3, IC$\sub$50/= 0,65 $\mu\textrm{m}$) against the vanilloid receptor in a Ca$\^$2+/ -influx assay.

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Synthesis and Herbicidal Activity of New 1-(4-chloro-2-fluoro-5-propargyloxyphenyl)-3-thiourea Derivatives (새로운 1-(4-chloro-2-fluoro-5-propargyloxyphenyl)-3-thiourea 유도체의 합성과 제초활성)

  • Park, Kwaun-Yong;Song, Jong-Hwan;Jeon, Dong-Ju;Soung, Min-Gyu;Sung, Nack-Do
    • The Korean Journal of Pesticide Science
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    • v.12 no.2
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    • pp.103-110
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    • 2008
  • To develop the third generation herbicidal cyclic imide (Cyl) derivatives, the new 1-(4-chloro-2-fluoro-5-propargyloxyphenyl)-3-thiourea derivatives were synthesized and measured their herbicidal activities ($pI_{50}$) in vivo (preemergence) against rice plant (Orysa Sativa) and barnyard grass (Echinochlor crus-galli). The synthetic yields (%) of aryl derivatives (21-40) in general was higher than that of alkyl derivatives (1-20). In case of alkyl derivatives, the synthetic yield depended on the structural forms of alkyl amine groups. From the results of correlation analysis between herbicidal activities and substituents, the compound 8 and 24 showed the highest herbicidal activity against the shoot and root of barnyard grass. Especially, the compounds 11 and 6 showed the selective herbicidal activities between rice plant and barnyard grass.

Substrate Specificity of Human Flavin-containing monooxygenase 1 for Thiocarbamides

  • Jung, Ki-Hwa;D. M. Ziegler;Kim, Young-Mi
    • Proceedings of the Korea Society of Environmental Toocicology Conference
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    • 2001.05a
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    • pp.124-124
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    • 2001
  • Microsomes isolated from Spodoptera frugiperda (Sf)9 cells infected wi th human FM01 recombinant baculovirus catalyzed the NADPH- and 02-dependent oxidation of methimazole, thiourea, and phenylthiourea. However there was no detectable activity with 1,3-diphenylthiourea or larger thiocarbamides. Microsomes from control Sf9 cells were devoid of methimazole or thiourea S-oxygenase activity. (omitted)

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Colorimetric and Fluorescent Recognition of Fluoride by a Binaphthol Thioureido Derivative

  • Tang, Lijun;Wang, Nannan;Guo, Jiaojiao
    • Bulletin of the Korean Chemical Society
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    • v.33 no.7
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    • pp.2145-2148
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    • 2012
  • A new thiourea based receptor (1) was synthesized and applied to fluoride ion recognition in acetonitrile solution. Receptor 1 displayed dual changes in absorption and fluorescence emission intensities selectively for fluoride ions. The interaction of 1 with fluoride undergoes a deprotonation process that is confirmed by $^1H$ NMR titration.

The Optimization of Silver Leaching from the Samjo Mine Concentrate by Thiourea (티오요소를 이용한 삼조광업 정광으로부터 은 용출 최적화)

  • Yang, Gwon-Seung;Kim, Bong-Ju;Choi, Nag-Choul;Park, Cheon-Young
    • Journal of the Mineralogical Society of Korea
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    • v.26 no.1
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    • pp.1-8
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    • 2013
  • This study was carried out to test the possibility of using an environmentally friendly method of leaching silver concentrate from the Samjo mine. The Samjo mine ore contained minerals such as pyrite, chalcopyrite, galena, arsenopyrite, and sphalerite. The concentrate samples tested with the thiourea solution were roasted at $750^{\circ}C$. The results of different experimental conditions showed that the highest silver leaching rate was obtained when the concentration of thiourea was at 0.8 g with ferric sulfate at 0.425 g and the leaching temperature at $60^{\circ}C$. The Ag leaching rate obtained was 91.5% at a pulp density of 10%. However, in the XRD analysis, peaks of pyrite, galena, and hematite were still found in the leached solid residues in which the Ag leaching rate was the highest. it is expected that the unrecovered silver in the solid residue can be lost.

The Crystal and Molecular Structure of Thiosinamine (Thiosinamine의 결정 및 분자구조)

  • Shin, Hyun-So;Koo, Chung-Hoe;Lee, Soon-Won
    • Journal of the Korean Chemical Society
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    • v.28 no.4
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    • pp.205-209
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    • 1984
  • The crystal and molecular structure of thiosinamine, $H_2NCSNHCH_2CHCH_2$, has been determined by X-ray diffraction method. The crystals are monoclinic, space group $P2_1/a$ with four molecules in a unit cell of dimensions, a = 9.819(3), b = 8.553(3), c = 9.170(2)${\AA}$, ${\beta}$ = 127.3(1)$^{\circ}$, and z = 4. Intensity data for 814 reflections were collected with a Rigaku-Denki automatic four circle diffractometer. The structure was solved by direct and Fourier methods. Refinements were carried out by full matrix least-squares method to a final R value of 0.046. The thiourea unit is planar, and the bond lengths and angles in that unit agree well with those in the compounds which contain a thiourea moiety. The molecules are linked together by the two patterns of N-H${\cdots}$S hydrogen bonds along the b-axis.

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