SU914545A1 - Process for producing vinyl chloride - Google Patents
Process for producing vinyl chloride Download PDFInfo
- Publication number
- SU914545A1 SU914545A1 SU802915656A SU2915656A SU914545A1 SU 914545 A1 SU914545 A1 SU 914545A1 SU 802915656 A SU802915656 A SU 802915656A SU 2915656 A SU2915656 A SU 2915656A SU 914545 A1 SU914545 A1 SU 914545A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- vinyl chloride
- catalyst
- producing vinyl
- dichloroethane
- chloride
- Prior art date
Links
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 title claims description 13
- 238000000034 method Methods 0.000 title claims description 10
- 239000003054 catalyst Substances 0.000 claims description 17
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 claims description 8
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims description 6
- 238000007033 dehydrochlorination reaction Methods 0.000 claims description 4
- 239000011777 magnesium Substances 0.000 claims description 3
- 229910001629 magnesium chloride Inorganic materials 0.000 claims description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052782 aluminium Inorganic materials 0.000 claims description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- 239000003607 modifier Substances 0.000 claims 2
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 101000581326 Homo sapiens Mediator of DNA damage checkpoint protein 1 Proteins 0.000 description 2
- 102100027643 Mediator of DNA damage checkpoint protein 1 Human genes 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229960003750 ethyl chloride Drugs 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Изобретение относится к синтезу хлористого винила, который находит применение в производстве полимерных материалов.The invention relates to the synthesis of vinyl chloride, which is used in the manufacture of polymeric materials.
Известен промышленный способ получения винилхлорида термическим дегидрохлорированием 1 ,2-дихлорэтана при 550° С [13.A known industrial method of producing vinyl chloride by thermal dehydrochlorination of 1, 2-dichloroethane at 550 ° C [13.
Недостатками способа являются сложность аппаратурного оформления, обусловленная применением высоких температур, и недостаточно высокая производительность процесса.The disadvantages of the method are the complexity of the hardware, due to the use of high temperatures, and the insufficiently high productivity of the process.
Наиболее близким к предлагаемому по технической сущности и достигаемому результату является способ получения винилхлорида дегидрохлорированием 1,2-дихлорэтана при 400450°С, в присутствии катализатора никель на окиси алюминия. Конверсия дихлорэтана 94-97%, селективность образования винилхлорида 9θ% ί 23.Closest to the proposed technical essence and the achieved result is a method for producing vinyl chloride by dehydrochlorination of 1,2-dichloroethane at 400-450 ° C, in the presence of a nickel on alumina catalyst. Dichloroethane conversion 94-97%, vinyl chloride selectivity 9θ% лорида 23.
Недостатками известного способа являются применение достаточно вы2 соких температур, а также необходимость стадии обработки используемого катализатора водородом для перевода его в активную форму. Все это в целом усложняет технологию процесса.The disadvantages of the known method are the use of sufficiently high temperatures, as well as the necessity of the stage of processing the used catalyst with hydrogen to convert it to the active form. All this in general complicates the process technology.
Цель - упрощение технологии процесса.The goal is to simplify process technology.
Поставленная цель достигается способом получения винилхлорида, состоящим в том, что 1,2-дихлорэтан подвергают дегидрохлорированию при 300-400°С в присутствии катализаторахлорида магния на окиси алюминия, при атомном соотношении магния и алюминия в используемом катализат торе (0,2-0,5):1.The goal is achieved by the method of producing vinyl chloride, which consists in the fact that 1,2-dichloroethane is subjected to dehydrochlorination at 300-400 ° C in the presence of magnesium chloride catalysts on aluminum oxide, with an atomic ratio of magnesium and aluminum in the used catalyst (0.2-0, 5): 1.
Для приготовления катализатора могут быть использованы <Г - и Ц, модификации А 1^3. Катализатор готовят путем пропитки гранул окиси алюминия водным раствором хлорида магния с последующим упариванием раствора, сушкой и прокаливанием кон-4 з 914545 4 ;For the preparation of the catalyst can be used <G - and C, modifications A 1 ^ 3. The catalyst is prepared by impregnating the alumina granules with an aqueous solution of magnesium chloride, followed by evaporation of the solution, drying and calcining con-4 3 914545 4;
т'актной массы на воздухе при 500еС в течение 4 ч. Состав катализатора может варьироваться в пределах Мд: А1 (0,2-0,5) :*1, г-ат. Регенерацию катализатрра осуществляют путем выжигания кокса кислородом воздуха при 35О°С.. t'aktnoy mass in air at 500 e C for 4 hours the catalyst composition may vary within a Mg: A1 (0.2-0.5): 1 *, g-at. Catalyst catalyst regeneration is carried out by burning coke with atmospheric oxygen at 35 ° C.
Предлагаемый способ получения винилхлорида проверяют в лабораторных условиях.The proposed method for producing vinyl chloride is tested in laboratory conditions.
Пример 1. Катализатор МдС12/А1203, Мд : А1 0,2:1. Опыт проводят на установке проточного типа со стационарным слоем катализатора. 8 пирексный реактор, снабженный карманом для термопары, помещают 9 мл катализатора (размер зерна 0,8-1,5 мм), установку продувают азотом и устанавливают в зоне катализатора температуру 400°С. Подачу 1,2-дихлорэтана осуществляют шприцдоЗатором с объемной скоростью 1 ,'13 4~ί Реакцию проводят в течение двух часов.Example 1. The catalyst MDC1 2 / A1 2 0 3 , MD: A1 0.2: 1. The experiment is carried out on a flow-through installation with a stationary catalyst bed. 8, a pyrex reactor equipped with a thermocouple pocket was placed with 9 ml of catalyst (grain size 0.8-1.5 mm), the plant was purged with nitrogen, and a temperature of 400 ° C was set in the catalyst zone. The supply of 1,2-dichloroethane is carried out by a syringe with a space velocity of 1, '13 4 ~ ί. The reaction is carried out for two hours.
Продукты реакции анализируют методами газо-жидкостной и газо-абсорбционной хроматографии.The reaction products are analyzed by gas-liquid and gas absorption chromatography.
П р и м е р 2. Катализатор МдС12/Д1а03, Мд:А1 0,5:1.PRI me R 2. Catalyst MDC1 2 / D1 a 0 3 , Md: A1 0.5: 1.
Условия проведения опыта аналогичны примеру 1, за исключением температуры реакции, которая составляет 35О°С.The conditions of the experiment are similar to example 1, except for the reaction temperature, which is 35 ° C.
ПримерЗ. Катализатор ,МдС1г/А1г03, Мд:А1 0,5:1.Example Z. Catalyst, MdC1 g / A1 g 0 3 , Md: A1 0.5: 1.
Условия проведения опыта аналогичны примеру 1 за исключением температуры реакции, которая составляет 300сС.Conditions of the experiment analogous to Example 1 except for the reaction temperature which is 300 C.
В табл.1 приведены результатыTable 1 shows the results
В табл.2 приведены данные материального баланса по примерам.Table 2 shows the material balance data by examples.
Таблица 2table 2
* Без учета хлористого водорода,* Excluding hydrogen chloride,
Сумма метана, пропилена, СО, СО^, ацетилена и этилена.The sum of methane, propylene, CO, CO ^, acetylene and ethylene.
Прочие - легкая фракция с температурой выкипания выше температуры кипения винилхлорида.Others - a light fraction with a boiling point above the boiling point of vinyl chloride.
Claims (1)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU802915656A SU914545A1 (en) | 1980-02-07 | 1980-02-07 | Process for producing vinyl chloride |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU802915656A SU914545A1 (en) | 1980-02-07 | 1980-02-07 | Process for producing vinyl chloride |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU914545A1 true SU914545A1 (en) | 1982-03-23 |
Family
ID=20892111
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU802915656A SU914545A1 (en) | 1980-02-07 | 1980-02-07 | Process for producing vinyl chloride |
Country Status (1)
| Country | Link |
|---|---|
| SU (1) | SU914545A1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101198575B (en) * | 2005-11-17 | 2012-12-26 | Lg化学株式会社 | Apparatus for producing vinyl chloride by pyrolysis of 1,2-dichloroethane and method for producing vinyl chloride using the same |
-
1980
- 1980-02-07 SU SU802915656A patent/SU914545A1/en active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101198575B (en) * | 2005-11-17 | 2012-12-26 | Lg化学株式会社 | Apparatus for producing vinyl chloride by pyrolysis of 1,2-dichloroethane and method for producing vinyl chloride using the same |
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