• 자원리싸이클링
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• 제10권3호
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• pp.60-65
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• 2001

폴리염화비닐(PVC)을 0~2 M NaOH수용액중에서 반응온도 $200~250^{\circ}C$, 반응시간 0~5시간으로 수열처리한 경우 PVC의 탈염화수소속도에 관해서 조사했다 수중에서는 PVC분말의 탈염화수소반응은 외견상 0차반응으로 진행되며, 이때의 활성화에너지는 약 46 kcal/mol이다. NaOH중에서의 탈염화수소에서는 NaOH농도가 0.5 M까지는 탈염화수소반응은 촉진되어지며 탈염화수소반응은 외 견상 1차반응으로 진행되었다. 또한 0.5M이상에서는 반응속도는 거의 일정했다. 0.1 M 및 0.5M NaOH수용액중에서의 탈염화수소반응의 활성화에너지는 약 46 kcal/mol로서 수중의 경우와 거의 같았다.

• 약학회지
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• 제55권2호
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• pp.127-130
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• 2011

We synthesized new ${\alpha}$-amidoketenes using dehydrochlorination from anilines, triethylamine and malonyl dichloride under $0^{\circ}C$. The utility of ketenes in both laboratory and industrial practice was quickly recognized, and these species have been extensively utilized, including as pharmaceutical intermediates and anti-cancer agents. All synthetic process from anilines to ${\alpha}$-amidoketenes could be carried out by one-pot reaction. Synthetic ketenes 2a~f were identified using NMR and IR spectrum. Formation of ketenes was undertaken with dropping of malonyl dichloride at $0^{\circ}C$ in methylene chloride for 0.5~4 h. Using malonyl dichloride was better than using diethyl malonate as a synthetic reagents for the ketenes.

• Journal of Industrial and Engineering Chemistry
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• 제67권
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• pp.276-283
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• 2018

For the first time, polyvinyl chloride (PVC) was used as an easily-handled chlorine source for preparation of isotropic pitch-based carbon fiber (IPCF) incorporating ethylene bottom oil (EO) as a raw material. Pitch precursors were prepared by the chlorination-dehydrochlorination triggered by chlorine radicals originated from PVC; aromatization and poly-condensation reactions occurred by polyene-type radicals from PVC. Radical production and co-carbonization were facilitated by pretreatments of EO through vacuum distillation, bromination, and additional heat treatment. Pitches were prepared by the co-carbonization of pretreated EO and EO containing 20 wt% PVC, and had higher yields and better spinnability than those by simple distillation.

• 자원리싸이클링
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• 제10권1호
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• pp.25-31
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• 2001

폴리염화비닐(PVC) 64.5%, 프탈산디옥틸(DOP) 32.2%, 칼슘-아연 스테아린산 안정제 및 계면활성제 등으로 되어진 PVC 필름을 $H_2O$, $Ca(OH)_2$ 그리고 $H_2$$SO_4$용액중에서 반응온도 $200-250 ^{\circ}C$, 반응시간 0-12시간으로 수열처리하였을 경우 PVC의 탈염화수소 및 생성되는 탄소질에 관해서 조사했다. $ H_2$ $SO_4$의 경우에는 탈염화수소가 빨라 25$0^{\circ}C$, 3시간 이상에서는 탈염화수소율이 거의 100%에 도달했다. 또한 이들의 수열처리에서는 다공질의 탄소질이 생성되었고 온도가 높을수록, 그리고 반응시간이 길수록 이들의 세공경은 작아졌다. $Ca(OH)_2$의 경우에는 $225^{\circ}C$, 12시간에서는 약 5-10 $mu extrm{m}$정도의 세공이 생성되었다. 그리고 $H_2$$_SO4$의 경우에는 5M의 $_H2$$SO _4$로 12시간 처리하였을 경우 약1 $\mu\textrm{m}$정도가 되었다

• Bulletin of the Korean Chemical Society
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• 제2권3호
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• pp.83-85
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• 1981

Tetrachlorocyclopropene has been prepared smoothly by the dehydrochlorination of pentachlorocyclopropane which could be obtained easily from sodium trichloroacetate and trichloroethylene in 1,2-dimethoxyethane. By the reaction of aromatic hydrocarbons with tetrachlorocyclopropene and aluminium chloride, new substituted phenyltrichlorocyclopropene derivatives have been prepared. The structures of these compounds were characterized by means of spectroscopic methods.

• 대한전자공학회:학술대회논문집
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• 대한전자공학회 2001년도 The 6th International Symposium of East Asian Resources Recycling Technology
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• pp.154-158
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• 2001

The heat treatment of PVC film containing PVC 65%, DOP(Dioctyl Phthalate) 32% as plasticizer, Ca-Zn stearates and surface agent was peformed under several conditions to study the degradation behavior of PVC sheet. In the case of H$_2$SO$_4$, the dehydrochlorination was ca.100% at 25$0^{\circ}C$ for 3h. The char involving the smaller pores was produced with hydrothermal treatment. The pore size became small with increasing the treatment time and temperature. In the case of treatment with Ca(OH)$_2$, the sizes of pores produced in char were about sever ~ 10${\mu}{\textrm}{m}$ at 2$25^{\circ}C$ for 12h. In the case of H$_2$SO$_4$, the size of pores were about 1${\mu}{\textrm}{m}$ in 5M H$_2$SO$_4$for 12h.

• 대한전자공학회:학술대회논문집
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• 대한전자공학회 2001년도 The 6th International Symposium of East Asian Resources Recycling Technology
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• pp.746-750
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• 2001

The heat treatment of PVC film containing PVC 65%, DOP(Dioctyl Phthalate) 32% as plasticizer, Ca-Zn stearates and surface agent was peformed under several conditions to study the degradation behavior of PVC sheet. In the case of H$_2$SO$_4$, the dehydrochlorination was ca.100% at 25$0^{\circ}C$ for 3h. The char involving the smaller pores was produced with hydrothermal treatment. The pore size became small with increasing the treatment time and temperature. In the case of treatment with Ca(OH)$_2$, the sizes of pores produced in char were about sever ~ 10${\mu}{\textrm}{m}$ at 2$25^{\circ}C$ for 12h. In the case of H$_2$SO$_4$, the size of pores were about l${\mu}{\textrm}{m}$ in 5M H$_2$SO$_4$for 12h.

• 자원리싸이클링
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• 제11권2호
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• pp.14-19
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• 2002

PVC(polyvinyl chloride)sheet를 NaOH수용액 중에서 반응온도 $80~150^{\circ}C$, 반응시간 0~7시간으로 처리하여 가소제의 침출에 관해서 검토하였다. DOP의 가수분해에 의해서 생성된 프탈산 수율은 알카리촉매로써 NaOH농도의 증가와 온도의 상승으로 인해 증가하고, $150^{\circ}C$, 10M NaOH, 3시간이상에서 프탈산 수율은 거의 100%,에 달했다. 따라서 PVC sheet에 30% 포함되어져 있는 가소제는 알카리수용액 중에서 탈염화수소가 일어나기 이전에 가수분해되어졌다. 또한, PVC필름의 수열처리에서는 DOP의 가수분해로 인해 세공이 생성되었다.

• 공업화학
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• 제9권4호
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• pp.497-503
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• 1998

알루미나에 담지한 귀금속 촉매를 이용하여 1.2-dichloroethane의 산화분해반응을 수행하였다. 실험결과 전환율은 Ru > Pt > Pd $${\sim_=}$$ Rh 순으로 높게 나타났으나, 완전산화 반응이 일어날 때의 주생성물인 $CO_2$로의 전환율 및 선택도를 기준으로 활성을 비교할 때 Pt/alumina가 Ru/alumina보다 활성이 높게 나타났다. $CO_2$ 및 vinyl chloride가 반응 주생성물로 검출되었는데, 반응 생성물 분포로부터 1.2-dichloroethane의 분해반응 경로는 1단계로 dehydrochlorination에 의해 vinyl chloride가 생성된 후 2단계로 vinyl chloride가 $CO_2$로 oxidation됨을 알 수 있었다. 염소를 포함하고 있는 반응 주생성물인 HCl의 영향을 살펴보기 위하여 반응물에 HCl을 첨가하여 반응을 수행하였는데 $300^{\circ}C$ 이하에서는 HCl이 촉매 표면에 흡착함에 따라 표면의 산도를 증가시켜 1.2-dichloroethane의 전환율은 증가하지만 $300^{\circ}C$ 이상에서는 HCl과 촉매 표면과의 상호작용이 약해져 전환율에는 큰 영향을 주지 않았다. 또한 촉매 표면에 가역적으로 흡착된 HCl은 1.2-dichloroethane의 $CO_2$로의 완전산화 반응을 방해함을 확인하였다.

• Archives of Pharmacal Research
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• 제16권2호
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• pp.168-174
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• 1993

The michael adducts 2a, b were obtained from the reaction of the phenylacelyl derivative 1 with benzadehyde and p-anisaldehyde and p-anisaldehyde respectively. 2a and 2b were subjected to react with cyanoethanoic acid hydrazide, malononitrile, cyanothioacetamide, cyanoacetamide and 1, 1, 3-tricyano-2-amino propene to yield 4a-h and 5a, b respecitively. Hydrogen peroxide oxidation of 2a, b gave the aurone derivative 6a, b. The pyone derivatives 8a, b were obtained from 2a, b by addition of chioroacetyl chioride followed by dehydrochlorination.