SU668613A3 - Composition for obtaining internally plastified copolymer of vinyl chloride - Google Patents
Composition for obtaining internally plastified copolymer of vinyl chlorideInfo
- Publication number
- SU668613A3 SU668613A3 SU762391000A SU2391000A SU668613A3 SU 668613 A3 SU668613 A3 SU 668613A3 SU 762391000 A SU762391000 A SU 762391000A SU 2391000 A SU2391000 A SU 2391000A SU 668613 A3 SU668613 A3 SU 668613A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- vinyl chloride
- copolymer
- composition
- acrylate
- plastified
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F214/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
- C08F214/02—Monomers containing chlorine
- C08F214/04—Monomers containing two carbon atoms
- C08F214/06—Vinyl chloride
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Polymerisation Methods In General (AREA)
Description
Л6L6
фокислоты, 0,02 бутилированнного окситолуола, 300 мл нафты дл лаков и красок.phacacids, 0.02 bottled oxytoluene, 300 ml naphtha for varnishes and paints.
Реагенты перемешивают и нагревают при 110-160°в течение 3-5 ч, отгон ют в виде азеотропа 50 мл воды. Затем реагенты нагревают в токе азота при 180-220 С дл удалени нафты. Полученный масл нистый продукт промывают 5%-ным раствором гидроокиси натри , потом водой до тех пор, пока проба на лакмусовую бумагу не даст нейтральной реакции. Получают 836 г или 96% от теории продукта, имеющего мол. массу 570 (продукт А).The reactants are stirred and heated at 110-160 ° for 3-5 hours, 50 ml of water are distilled off as an azeotrope. The reagents are then heated in a stream of nitrogen at 180-220 ° C to remove naphtha. The oily product obtained is washed with 5% sodium hydroxide solution, then with water until the test for litmus paper is neutral. Receive 836 g or 96% of the theory of the product, having a mol. weight 570 (product A).
Пример 2. Получение терполимерной композиции винилхлорид - cлoжный эфир фумаровой кислоты - акрилатExample 2. Obtaining terpolymer composition of vinyl chloride - fumaric acid - ester acrylate
В бутыль емкостью 1,14 л помещают следующие реагенты: 300 г воды, 35 гThe following reagents are placed in a 1.14 L bottle: 300 g of water, 35 g
ОбраСостав загрузки зецThe composition of loading
65 ВХ/30 ЭГА/5 продукта А 70 ВХ/30 ЭГА (сравнительный) 70 ВХ/30 ЭГА (сравнительный)65 BX / 30 EGA / 5 product A 70 BX / 30 EGA (comparative) 70 BX / 30 EGA (comparative)
65 ВХ/35 продукта А (сравнительный )65 BX / 35 product A (comparative)
65 ВХ/25 ЭГА/10 продукта А 65 ВХ/ЗО ЭГА/5 фумарата 50 ВХ/35 ЭГА/15 ДБФ 65 ВХ/30 ГА/5 ЭГФ ВХ - винилхлорид, ЭГА - 2-Этилгек гексилфумарат, (Ф+А) - фумгграт + Пример 3. Смешивают 100 г каждого из образцов, приведенных в табл. 1 со следующими ингредиентами: 5 г эпоксидированного соевого масла, 1,5 г ®арий-кадмиевого стаПоказатель65 BX / 25 EGA / 10 product A 65 BX / ZO EGA / 5 fumarate 50 BX / 35 EGA / 15 DBF 65 BX / 30 HA / 5 EGF BX - vinyl chloride, EGA - 2-Ethylhexyl fumarate, (F + A) - fugggrata + Example 3. Mix 100 g of each of the samples listed in the table. 1 with the following ingredients: 5 g epoxidized soybean oil, 1.5 g stearate-cadmium staF.
Температурна гибкость по Клаш-Вергу,°Ф -30Temperature flexibility Klach-Verga, ° F -30
-19-nineteen
69 83 9569 83 95
8,48.4
247 147 187247 147 187
1 341 34
1%-ного раствора оксипропилметилцелллозы , 30 г 2-этилгексилакрилата и 5 г продукта А. Бутыль охлаждают до -15С в течение 2 ч.1% aqueous solution of hydroxypropyl methylcellulose, 30 g of 2-ethylhexyl acrylate and 5 g of product A. The bottle is cooled to -15 ° C for 2 hours.
Затем прибавл ют 2,5 мл 10%-ного раствора изопропилпероксикарбоната в гептане и 65 г винилхлорида. Бутыл запечатывают и закладывают в аппарат дл полимеризации, который привод т во вращение со скоростью 35 об/мин при нагревании до 45° С в течение 12 ч. После охлаждени до комнатной температуры бутыль вскрывают и провер ют отсутствие непрореагировавшего винилхлорида.Then 2.5 ml of a 10% solution of isopropyl peroxycarbonate in heptane and 65 g of vinyl chloride are added. The bottle is sealed and placed in a polymerization apparatus, which is rotated at a speed of 35 rpm when heated to 45 ° C for 12 hours. After cooling to room temperature, the bottle is opened and the absence of unreacted vinyl chloride is checked.
По данной методике готов т р д других композиций.According to this method, a number of other compositions are prepared.
Результаты приведены в табл .1.The results are shown in Table .1.
Таблица 1Table 1
Конечный составFinal composition
65 ВХ/36,5 (Ф+А) 64,6 ВХ/35,4 ЭГА 66,6 ВХ/33,4 ЭГФ65 BX / 36.5 (F + A) 64.6 BX / 35.4 EGA 66.6 BX / 33.4 EGF
65,3 ВХ/34,7 Ф-57065.3 BX / 34.7 F-570
62.4ВХ/37,6 (Ф+А)62.4BX / 37.6 (F + A)
65.5ВХ/34,5 (Ф+А)65.5BX / 34.5 (F + A)
61,4 ВХ/38,6(Ф+А) g 61.4 BX / 38.6 (F + A) g
-24-24
-24-24
-48-48
-32-32
5 6 72 34 595 6 72 34 59
Claims (3)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US61091075A | 1975-09-05 | 1975-09-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
SU668613A3 true SU668613A3 (en) | 1979-06-15 |
Family
ID=24446895
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU762391000A SU668613A3 (en) | 1975-09-05 | 1976-09-01 | Composition for obtaining internally plastified copolymer of vinyl chloride |
Country Status (24)
Country | Link |
---|---|
JP (1) | JPS5232094A (en) |
AU (1) | AU500800B2 (en) |
BE (1) | BE845793A (en) |
BR (1) | BR7605540A (en) |
CA (1) | CA1099449A (en) |
CH (1) | CH623835A5 (en) |
CS (1) | CS191986B2 (en) |
DD (1) | DD128365A5 (en) |
DE (1) | DE2639171C2 (en) |
EG (1) | EG13168A (en) |
FR (1) | FR2322894A1 (en) |
GB (1) | GB1517428A (en) |
HU (1) | HU174380B (en) |
IL (1) | IL49849A (en) |
IT (1) | IT1066283B (en) |
MX (1) | MX144414A (en) |
NL (1) | NL7608029A (en) |
NO (1) | NO146674C (en) |
PH (1) | PH14844A (en) |
PL (1) | PL103652B1 (en) |
RO (1) | RO77604A (en) |
SE (1) | SE7609703L (en) |
SU (1) | SU668613A3 (en) |
ZA (1) | ZA763740B (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5329221Y2 (en) * | 1973-09-29 | 1978-07-22 | ||
IL56417A (en) * | 1978-03-20 | 1982-11-30 | Stauffer Chemical Co | Vinyl film/substrate laminate |
CN103333281B (en) * | 2013-06-20 | 2015-07-15 | 无锡洪汇新材料科技股份有限公司 | Resin for blood transfusion tube/transfusion bag and preparation method thereof |
EP3168244B1 (en) * | 2015-06-05 | 2018-08-08 | LG Chem, Ltd. | Method of preparing vinyl chloride-based copolymer and vinyl chloride-based copolymer prepared thereby |
-
1976
- 1976-06-21 GB GB25703/76A patent/GB1517428A/en not_active Expired
- 1976-06-21 CA CA255,316A patent/CA1099449A/en not_active Expired
- 1976-06-21 IL IL49849A patent/IL49849A/en unknown
- 1976-06-23 ZA ZA763740A patent/ZA763740B/en unknown
- 1976-06-24 AU AU15254/76A patent/AU500800B2/en not_active Expired
- 1976-07-20 NL NL7608029A patent/NL7608029A/en not_active Application Discontinuation
- 1976-07-28 FR FR7622977A patent/FR2322894A1/en active Granted
- 1976-07-30 MX MX165724A patent/MX144414A/en unknown
- 1976-08-05 JP JP51093521A patent/JPS5232094A/en active Pending
- 1976-08-07 EG EG478/76A patent/EG13168A/en active
- 1976-08-10 RO RO7687263A patent/RO77604A/en unknown
- 1976-08-18 PL PL1976191878A patent/PL103652B1/en unknown
- 1976-08-24 BR BR7605540A patent/BR7605540A/en unknown
- 1976-08-26 CS CS765549A patent/CS191986B2/en unknown
- 1976-08-31 NO NO762987A patent/NO146674C/en unknown
- 1976-08-31 DE DE2639171A patent/DE2639171C2/en not_active Expired
- 1976-09-01 SU SU762391000A patent/SU668613A3/en active
- 1976-09-02 BE BE7000876A patent/BE845793A/en not_active IP Right Cessation
- 1976-09-02 DD DD7600194576A patent/DD128365A5/en unknown
- 1976-09-02 IT IT51114/76A patent/IT1066283B/en active
- 1976-09-02 PH PH18861A patent/PH14844A/en unknown
- 1976-09-02 SE SE7609703A patent/SE7609703L/en not_active Application Discontinuation
- 1976-09-03 CH CH1124876A patent/CH623835A5/en not_active IP Right Cessation
- 1976-09-03 HU HU76SA2971A patent/HU174380B/en unknown
Also Published As
Publication number | Publication date |
---|---|
NO146674B (en) | 1982-08-09 |
IL49849A (en) | 1979-05-31 |
EG13168A (en) | 1980-12-31 |
CH623835A5 (en) | 1981-06-30 |
ZA763740B (en) | 1977-05-25 |
DE2639171A1 (en) | 1977-03-24 |
AU500800B2 (en) | 1979-05-31 |
FR2322894B1 (en) | 1979-09-07 |
HU174380B (en) | 1979-12-28 |
FR2322894A1 (en) | 1977-04-01 |
BR7605540A (en) | 1977-08-09 |
AU1525476A (en) | 1978-01-05 |
NO146674C (en) | 1982-11-17 |
DE2639171C2 (en) | 1985-02-14 |
DD128365A5 (en) | 1977-11-16 |
NL7608029A (en) | 1977-03-08 |
SE7609703L (en) | 1977-03-06 |
MX144414A (en) | 1981-10-13 |
BE845793A (en) | 1977-03-02 |
CA1099449A (en) | 1981-04-14 |
PH14844A (en) | 1981-12-16 |
JPS5232094A (en) | 1977-03-10 |
NO762987L (en) | 1977-03-08 |
CS191986B2 (en) | 1979-07-31 |
PL103652B1 (en) | 1979-07-31 |
IT1066283B (en) | 1985-03-04 |
GB1517428A (en) | 1978-07-12 |
RO77604A (en) | 1981-11-04 |
IL49849A0 (en) | 1976-08-31 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
HUT53076A (en) | Process for producing tetrahydro-1-benz(c,d)indolepropionic acid sulfonamide derivatives and pharmaceutical compositions comprising such compounds | |
SU668613A3 (en) | Composition for obtaining internally plastified copolymer of vinyl chloride | |
US2683132A (en) | Stabilized relatively nonvolatile organic compositions containing bis (p-hydroxy aryl amides) of polybasic acids | |
AU5843780A (en) | Preparation of n-vinyl-n-alkyl carboxylic acid amides | |
US2395347A (en) | Sulphur-containing esters of hydrolyzed ethylene-vinyl organic ester interpolymers | |
US3931363A (en) | Color improvement of phosphate esters | |
US2813885A (en) | Process for making fatty peracids | |
US2630442A (en) | Organotin phosphate esters | |
US2017000A (en) | Silicon carboxylate and process of making the same | |
US3317576A (en) | Reaction products of antimony halides or oxides with thioglycollic mercapto-hydroxyalkanes | |
US2790785A (en) | Rubber stabilized with hydrocarbon tin mercapto alcohol esters | |
US3779962A (en) | Stabilizer-lubricant combinations for halogen-containing polymers | |
US2610202A (en) | Esters of polymers of maleic anhydride and beta-mercaptoethanol and process | |
Nightingale et al. | The Action of Sodium, Lithium and Potassium Phenylacetylene on Acid Derivatives | |
US3121111A (en) | Novel 4-thiohydantoic acids | |
KR880007454A (en) | Monoperoxalic acid ester, its preparation method and its use as a polymerization initiator | |
US4274991A (en) | Alkyl sulphonic acid phenyl esters substituted by carboxylic acid esters | |
GB681581A (en) | Improvements in or relating to resinous compositions | |
US3833631A (en) | Aluminum salts of esters as stabilizing agents for chlorinated vinyl polymers | |
US2779809A (en) | Acceleration of vulcanization by means of nu-mono-tertiary-alkyl-thiazoline-2-sulfenamides | |
US2418942A (en) | Method for producing polymeric materials containing sulfur | |
RU2076119C1 (en) | Polymer composition | |
US3007911A (en) | Method of sulfochlorinating hydrocarbons | |
US3111504A (en) | Process for the vulcanization of rubber | |
US2349774A (en) | Acetoxyamino acids and method for their preparation |