• Resources Recycling
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• v.10 no.3
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• pp.60-65
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• 2001

The PVC powder was treated at $200~250^{\circ}C$, in 0~2 M NaOH solutions for 0~5 h to study the kinetics of dehydrochlorination. In the case of water, the dehydrochlorination of PVC powder proceeded by the zero order reaction with X(the degree of dehydrochlorination), and the apparent activation energy was about 46 kcal/mol. The rate of dehydrochlorination increased with con-centration to 0.5 M NaOH, and proceeded by the first order reaction with X. And, the kinetics of dehydrochlorination was almost equal above 0.5 M NaOH. The apparent activation energies of dehydrochlorination in 0.1 M and 0.5 M NaOH was about 46 kcal/mol, respectively.

• YAKHAK HOEJI
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• v.55 no.2
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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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• v.67
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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.

• Resources Recycling
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• v.10 no.1
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• pp.25-31
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• 2001

The heat treatment of PVC film containing PVC 65ft, DOP (Dioctyl Phthalate) 32% as plasticizer, Ca-Zn stearates and sur-face agent was performed under several conditions to study the dehydrochlorination of PVC and char production. In the case of $H_2$ $SO_4$, the dehydrochlorination was ca.100% at $250^{\circ}C$ for 3h. The char involving the smaller pores was produced with hydro-thermal 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$ 225^{\circ}C$ for 12h. In the case of $_2$$SO_4$, the size of pores were about 1 $\mu\textrm{m}$ in 5M $_H2$$SO_4$for 12h.

• Bulletin of the Korean Chemical Society
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• v.2 no.3
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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.

• Proceedings of the IEEK Conference
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• 2001.10a
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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.

• Proceedings of the IEEK Conference
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• 2001.10a
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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.

• Resources Recycling
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• v.11 no.2
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• pp.14-19
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• 2002

PVC sheet was treated in O~10M NaOH solutions at $80~150^{\circ}C$ for O~7 hour, in order to study the leaching phenomena of plasticizer. The yield of phthalic acid produced by hydrolysis of DOP was increased greatly with increasing temperature and NaOH concentration by accelerating of alkali catalyst. The yield of phthalic acid was reached ca. 100% in 10M NaOH at $150^{\circ}C$ over 3 hours. Therefore, the plasticizer containing 30% in PVC sheet could be hydrolyzed in alkali solutions before the occurrence of dehydrochlorination. Besides, in the thermal reaction, the pores were produced in the PVCsheet by the hydrolysis of DOP.

• Applied Chemistry for Engineering
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• v.9 no.4
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• pp.497-503
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• 1998

The catalytic oxidation of 1.2-dichloroethane was investigated over precious metal supported on alumina using a fixed bed microreactor. Among the catalysts tested, the conversion of 1.2-dichloroethane decreased in the following order : Ru > Pt > Pd $${\sim_=}$$ Rh and Pt was found to be the most active catalyst for the complete oxidation of 1.2-dichloroethane to $CO_2$. Major products containing carbon were vinyl chloride and $Co_2$ at temperature ranging from 200 to $400^{\circ}C$. The presence of vinyl chloride in products suggests that the first step in the oxidation of 1.2-dichloroethane is dehydrochlorination and the second is oxidation of vinyl chloride to $CO_2$. To investigate the effect of HCl on the activity of the complete oxidation, some experiments were conducted by adding HCl to the feed. The presence of HCl increased the conversion of 1.2-dichloroethane below $300^{\circ}C$ owing to the increase of surface acidity, but it didn't affect the conversion above $300^{\circ}C$. The reversible adsorption of HCl onto catalyst surface inhibited the complete oxidation to $CO_2$.

• Archives of Pharmacal Research
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• v.16 no.2
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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.