• 한국응용과학기술학회지
• /
• 제14권2호
• /
• pp.93-102
• /
• 1997

Isothiazoline derivatives is widely used to food, medical drug and industrial goods, cosmetics etcs, and it makes to restrain and to sterilize a breeding of microbe as a preservative and a sterilizing agent. It differs with the raw material of paraoxybenzoic acid derivatives or imidazolydinyl urea to be in use at present, on the efficacy and effect, and has various characteristics. This synthesis makes 3,3'-dithiodipropionic chloride to add a thionyl chloride in 3,3'-dithiodipropionic acid, and 3,3'-dithiodipropionic methyl amide makes to synthesize in a reflux reaction the mono methyl amine to 3,3'-dithiodipropionic chloride. And last synthesis becomes to make chlorination-cyclization molecule doing a reflux reaction in the temperature of $90{\sim}100^{\circ}C$ to mix excessively thionyl chloride and ethylene dichloride to 3,3'-dithiodipropionic methyl amide. The last synthesis material has got in the mixture of 5-chloro-2-methyl-4-isothiazoline-3-one and 2-methyl-4-isothiazoline-3-one, and it is so-called isothiazoline derivatives. The purification of isothiazoline derivatives makes to fuse in ethyl acetate, and makes to decolorize and to deodorize in recrystallization. This experiment has been in synthesis and purification of isothiazoline derivatives, and has tried to measure on the antisepsis and sterilization function of microbe according to pH or content change.

• Bulletin of the Korean Chemical Society
• /
• 제15권6호
• /
• pp.456-460
• /
• 1994

Catalytic effects of various cobalt phenylporphyrin compounds on the reduction of thionyl chloride at glassy carbon electrode have been evaluated by determining kinetic parameters with cyclic voltammetric techniques. The concentration of catalysts and the electrode immersion time have been found to affect the catalyst performance strongly, leading to a conclusion that the compounds are first adsorbed at the electrode surface and act as catalysts. Significant improvements in cell performance have been noted in terms of both exchange rate constants of up to 3 times and current densities of up to 150% at glassy carbon electrode.

• Bulletin of the Korean Chemical Society
• /
• 제14권3호
• /
• pp.313-315
• /
• 1993

• 폴리머
• /
• 제34권3호
• /
• pp.198-201
• /
• 2010

탄소나노튜브의 응집력을 완화하기 위한 표면 개질과 고분자 소재와의 상용성을 유도하기 위하여, 친수성 고분자를 도입하는 연구를 진행하였다. 산처리를 통한 표면 기능화를 시행하였으며, 카복실기 도입 탄소나노튜브를 thionyl chloride을 사용하여 acyl chloride로 치환한 후 저분자량의 아민 말단 poly(ethylene oxide)를 공유결합으로 도입하였다. TGA를 통하여 탄소나노튜브 표면에 도입된 고분자의 함량을 계산하였으며, 탄소나노튜브 표면에 도입된 고분자의 표면 형상을 SEM과 TEM을 통하여 직경이 증가하는 것을 확인할 수 있었다.

• 대한화학회지
• /
• 제49권5호
• /
• pp.470-472
• /
• 2005

• Korean Chemical Engineering Research
• /
• 제53권1호
• /
• pp.83-90
• /
• 2015

본 연구에서는 multi-walled carbon nanotube (MWCNT) 표면에 자유 라디칼 중합 가능한 methacrylate기를 다량으로 도입하기 위한 연구를 수행하였다. 먼저, MWCNT 표면에 카르복실기(-COOH)를 도입하기 위하여 황산과 질산의 혼산으로 초음파로 처리하면서 2시간 산화시켜 MWCNT-COOH를 합성하였다. 합성된 MWCNT-COOH를 염화티오닐(thionyl chloride)와 반응시켜 MWCNT-COCl을 합성하고, triethylenetetramine (TETA)와 반응시켜 MWCNT-$NH_2$를 합성하였다. 합성된 MWCNT-$NH_2$와 3-(acryloyloxy)-2-hydroxypropyl methacrylate (AHM)의 투입 몰 비를 변화시키면서 Michael 부가 반응으로 MWCNT 표면에 methacrylate기가 도입된 MWCNT-AHM을 합성하였다. MWCNT의 표면 개질정도는 fourier transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA)와 원소분석(elemental analysis, EA) 분석을 통해 개질 반응의 진행 정도와 최적 개질 조건을 확인하였다. 그 결과 MWCNT-$NH_2$에 접목되어 있는 TETA에 대하여 AHM의 반응 몰 비를 1:10로 하고 8시간 반응시켰을 때 methacrylate기가 가장 많이 도입되는 조건임을 확인하였다.

• 전기화학회지
• /
• 제5권4호
• /
• pp.178-182
• /
• 2002

The electrochemical behavior of binder-free carbon anode, comprising of only artificial and natural graphite (AG and NG) particles, for intercalation and deintercalation of lithium ion $(Li^+)$ in aluminum chloride (AICI_3)-I-ethyl­3-methylimidazolium chloride (EMIC)-lithium chloride (LiCl)-thionyl chloride $(SOCI_2)$ room-temperature molten salt (RTMS) was studied. Binder-free carbon electrodes were fabricated using electrophoretic deposition (EPD) method. The binder-free carbon anodes provided a relatively flat charge and discharge potentials $(0\;to\;0.2V\;vs.\;Li/Li^+)$ and current capabilities $(250-340mAh{\cdot}g^{-1})$ for the intercalation and deintercalation of $Li^+$. Stability of the binder-free carbon anodes for intercalation and deintercalation of 50 cycles was confirmed.

• 대한화학회지
• /
• 제57권2호
• /
• pp.221-226
• /
• 2013

A series of some novel 2-[5-(substituted phenyl)-[1,3,4]oxadiazol-2-yl]-benzoxazoles were synthesized by using benzoxazole-2-carboxylic acid on reaction with thionyl chloride in presence of ethanol solvent at room temperature gave benzoxazole-2-carbonyl chloride, which is turned into benzoxazole-2-carboxylic acid hydrazide on reaction with hydrazine hydrate in ethanol solvent under reflux. The subsequent treatment of benzoxazole-2-carboxylic acid hydrazide with an appropriate aromatic carboxylic acid in presence of polyphosparic acid under reflux afforded the title compounds. The chemical structures of the newly synthesized compounds were elucidated by their IR, $^1H$ NMR and Mass spectral data analysis. Further the compounds are used to find out their ability towards anti microbial and nematicidal activity.

• Elastomers and Composites
• /
• 제47권4호
• /
• pp.355-363
• /
• 2012

2,2-Bis(3-amino-4-hydroxyphenyl)hexafluoropropane 와 방향족 디이미드-디카르복실산을 thionyl chloride, triethyl amine 및 NMP 하에서 직접 중축합하여 trifluoromethyl group을 포함하는 일련의 poly(hydroxyamide)s(PHAs)를 제조 하였다. PHAs은 $35^{\circ}C$ DMAc 용액에서 0.54-0.96 dL/g의 고유점도를 보였다. 모든 PHAs은 여러 종류의 유기용매에 쉽게 용해되었으나, PBOs은 황산에 부분적으로 용해되는 것을 제외하고, 전혀 용해되지 않았다. PHAs은 열적고리화 반응에 의해서 흡열과 함께 PBOs로 전환되었다. PHAs의 최대 중량손실온도는 $559-567^{\circ}C$의 영역을 보였고, poly(benzoxazole imide)s(PBOs)은 47-59%의 비교적 높은 char 수득율을 보였다. PBOs의 Pyrolysis Combustion Flow Calorimeter(PCFC) 결과에서 12-19 W/g의 HRR 과 2.7-3.6 kJ/g의 total HR을 보였다. PBO 1의 HRR은 PBO 3 의 HRR (19 W/g)보다 37 % 낮은 12 W/g의 가장 낮은 값을 보였다.

• 약학회지
• /
• 제40권6호
• /
• pp.621-624
• /
• 1996

Betaine was treated with hydrochloric acid and then with sodium borohydride to give a hydroxy compound 2. The reaction of 2 with thionyl chloride followed by thiourea led a comp ound 5. Oxidation of compound 2 with pyridinium dichromate(PDC) and succesive treatment with Lawesson's reagent also afforded the same compound 5. Cleavage of N-C14 bond compound of 7 was carried out via two reaction sequence from the compound 4. Finally, compound 10 was sythesized by a series of transformations from the compound 4.