SU665811A3 - Композици на основе поливинилхлорида - Google Patents
Композици на основе поливинилхлоридаInfo
- Publication number
- SU665811A3 SU665811A3 SU762409354A SU2409354A SU665811A3 SU 665811 A3 SU665811 A3 SU 665811A3 SU 762409354 A SU762409354 A SU 762409354A SU 2409354 A SU2409354 A SU 2409354A SU 665811 A3 SU665811 A3 SU 665811A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- polyvinyl chloride
- ester
- composition
- compound
- salt
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 18
- 229920000915 polyvinyl chloride Polymers 0.000 title claims description 8
- 239000004800 polyvinyl chloride Substances 0.000 title claims description 8
- 239000003381 stabilizer Substances 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 6
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 230000000087 stabilizing effect Effects 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 3
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 claims description 3
- 150000002894 organic compounds Chemical class 0.000 claims description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 3
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 2
- 150000002148 esters Chemical class 0.000 claims 2
- 125000000686 lactone group Chemical group 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- -1 3,4-epoxycyclohexylmethyl ester Chemical class 0.000 claims 1
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 230000006378 damage Effects 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 150000002596 lactones Chemical class 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 230000006641 stabilisation Effects 0.000 claims 1
- 238000011105 stabilization Methods 0.000 claims 1
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- HPEUJPJOZXNMSJ-UHFFFAOYSA-N Methyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC HPEUJPJOZXNMSJ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 229930188620 butyrolactone Natural products 0.000 description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
- 239000008116 calcium stearate Substances 0.000 description 2
- 235000013539 calcium stearate Nutrition 0.000 description 2
- 238000003490 calendering Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- RMBQKTUTSBSOPP-UHFFFAOYSA-N 3-benzoyloxolan-2-one Chemical compound C=1C=CC=CC=1C(=O)C1CCOC1=O RMBQKTUTSBSOPP-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000004801 Chlorinated PVC Substances 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229920000457 chlorinated polyvinyl chloride Polymers 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- CAMHHLOGFDZBBG-UHFFFAOYSA-N epoxidized methyl oleate Natural products CCCCCCCCC1OC1CCCCCCCC(=O)OC CAMHHLOGFDZBBG-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 238000001175 rotational moulding Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Polyesters Or Polycarbonates (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7531949A FR2328014A1 (fr) | 1975-10-14 | 1975-10-14 | Stabilisation des polymeres du chlorure de vinyle a l'aide de composes lactoniques |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU665811A3 true SU665811A3 (ru) | 1979-05-30 |
Family
ID=9161363
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU762409354A SU665811A3 (ru) | 1975-10-14 | 1976-10-13 | Композици на основе поливинилхлорида |
Country Status (27)
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2042562B (en) * | 1979-02-05 | 1983-05-11 | Sandoz Ltd | Stabilising polymers |
| BE881495A (fr) * | 1979-02-05 | 1980-08-01 | Sandoz Sa | Procede de stabilisation de matieres organiques polymeres |
| DE2910402A1 (de) * | 1979-03-16 | 1980-09-25 | Basf Ag | Farbstabilisierte, nichtionische tenside und alkalische reinigerformulierungen, die diese tenside enthalten |
| JPS5857459B2 (ja) * | 1979-07-31 | 1983-12-20 | 大日本インキ化学工業株式会社 | 耐熱性可塑剤 |
| DE4018293A1 (de) * | 1990-06-07 | 1991-12-12 | Neynaber Chemie Gmbh | Ketofettsaeureglyceride enthaltende stabilisatoren fuer ca/zn-stabilisierte pvc-formmassen |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB634762A (en) * | 1948-01-13 | 1950-03-29 | Distillers Co Yeast Ltd | Improvements in or relating to the stabilisation of vinylidene chloride resins |
| US3055861A (en) * | 1958-02-19 | 1962-09-25 | Union Carbide Corp | Stabilized acrylonitrile vinyl or vinylidene copolymer solutions |
| US2971962A (en) * | 1959-01-22 | 1961-02-14 | United States Steel Corp | Method of making the lactone of 2-hydroxybiphenyl-2'-carboxylic acid |
| US3223660A (en) * | 1960-05-27 | 1965-12-14 | Nopco Chem Co | Stabilization of vinyl resins with tetrahydropyrans and organic metal salts |
| US3644573A (en) * | 1969-07-02 | 1972-02-22 | Eastman Kodak Co | Heat stabilization of polyesters |
-
1975
- 1975-10-14 FR FR7531949A patent/FR2328014A1/fr active Granted
-
1976
- 1976-10-07 FI FI762859A patent/FI64387C/fi not_active IP Right Cessation
- 1976-10-11 AR AR265047A patent/AR219287A1/es active
- 1976-10-11 DE DE2645870A patent/DE2645870C3/de not_active Expired
- 1976-10-12 BR BR7606817A patent/BR7606817A/pt unknown
- 1976-10-12 JP JP51122214A patent/JPS5247847A/ja active Pending
- 1976-10-12 GR GR51927A patent/GR60338B/el unknown
- 1976-10-12 LU LU75982A patent/LU75982A1/xx unknown
- 1976-10-12 AU AU18588/76A patent/AU513658B2/en not_active Expired
- 1976-10-12 ZA ZA766056A patent/ZA766056B/xx unknown
- 1976-10-12 GB GB42334/76A patent/GB1532478A/en not_active Expired
- 1976-10-12 US US05/731,435 patent/US4132703A/en not_active Expired - Lifetime
- 1976-10-12 NZ NZ182308A patent/NZ182308A/xx unknown
- 1976-10-12 DD DD195232A patent/DD126573A5/xx unknown
- 1976-10-13 CA CA263,279A patent/CA1093731A/fr not_active Expired
- 1976-10-13 CS CS766627A patent/CS222231B2/cs unknown
- 1976-10-13 NO NO763484A patent/NO144971C/no unknown
- 1976-10-13 CH CH1296776A patent/CH597304A5/xx not_active IP Right Cessation
- 1976-10-13 SE SE7611371A patent/SE415568B/xx not_active IP Right Cessation
- 1976-10-13 SU SU762409354A patent/SU665811A3/ru active
- 1976-10-13 MX MX764974U patent/MX3594E/es unknown
- 1976-10-13 PT PT65705A patent/PT65705B/pt unknown
- 1976-10-13 DK DK460276A patent/DK460276A/da not_active Application Discontinuation
- 1976-10-14 NL NL7611358.A patent/NL162679C/xx not_active IP Right Cessation
- 1976-10-14 BE BE171504A patent/BE847272A/xx not_active IP Right Cessation
- 1976-10-14 IT IT28337/76A patent/IT1068945B/it active
- 1976-10-14 ES ES452378A patent/ES452378A1/es not_active Expired
Also Published As
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