GB1091521A - Esters of polymers - Google Patents
Esters of polymersInfo
- Publication number
- GB1091521A GB1091521A GB22150/63A GB2215063A GB1091521A GB 1091521 A GB1091521 A GB 1091521A GB 22150/63 A GB22150/63 A GB 22150/63A GB 2215063 A GB2215063 A GB 2215063A GB 1091521 A GB1091521 A GB 1091521A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- oil
- polyol
- ester
- long chain
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 150000002148 esters Chemical class 0.000 title abstract 6
- 229920000642 polymer Polymers 0.000 title abstract 3
- 239000002253 acid Substances 0.000 abstract 8
- 229920005862 polyol Polymers 0.000 abstract 6
- 150000003077 polyols Chemical class 0.000 abstract 6
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 abstract 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 4
- -1 acrylate ester Chemical class 0.000 abstract 4
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 abstract 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 abstract 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 3
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 abstract 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract 2
- 229920001577 copolymer Polymers 0.000 abstract 2
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 2
- 229930195729 fatty acid Natural products 0.000 abstract 2
- 239000000194 fatty acid Substances 0.000 abstract 2
- 150000004665 fatty acids Chemical class 0.000 abstract 2
- 239000003921 oil Substances 0.000 abstract 2
- 235000019198 oils Nutrition 0.000 abstract 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 abstract 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 abstract 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 abstract 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
- 239000005711 Benzoic acid Substances 0.000 abstract 1
- 239000004342 Benzoyl peroxide Substances 0.000 abstract 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 244000068988 Glycine max Species 0.000 abstract 1
- 235000010469 Glycine max Nutrition 0.000 abstract 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 abstract 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 abstract 1
- 235000021355 Stearic acid Nutrition 0.000 abstract 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 abstract 1
- 239000000654 additive Substances 0.000 abstract 1
- 238000007605 air drying Methods 0.000 abstract 1
- 150000007824 aliphatic compounds Chemical class 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 235000010233 benzoic acid Nutrition 0.000 abstract 1
- 235000019400 benzoyl peroxide Nutrition 0.000 abstract 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 abstract 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
- 239000004359 castor oil Substances 0.000 abstract 1
- 235000019438 castor oil Nutrition 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 239000003240 coconut oil Substances 0.000 abstract 1
- 235000019864 coconut oil Nutrition 0.000 abstract 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 abstract 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 abstract 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 abstract 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 abstract 1
- TZMQHOJDDMFGQX-UHFFFAOYSA-N hexane-1,1,1-triol Chemical compound CCCCCC(O)(O)O TZMQHOJDDMFGQX-UHFFFAOYSA-N 0.000 abstract 1
- 229920001519 homopolymer Polymers 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 0.000 abstract 1
- 239000000944 linseed oil Substances 0.000 abstract 1
- 235000021388 linseed oil Nutrition 0.000 abstract 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 abstract 1
- 239000012454 non-polar solvent Substances 0.000 abstract 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 abstract 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 1
- 239000000049 pigment Substances 0.000 abstract 1
- 239000002798 polar solvent Substances 0.000 abstract 1
- 239000005076 polymer ester Substances 0.000 abstract 1
- 230000000379 polymerizing effect Effects 0.000 abstract 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 abstract 1
- 239000001294 propane Substances 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000008117 stearic acid Substances 0.000 abstract 1
- 239000003784 tall oil Substances 0.000 abstract 1
- 239000004408 titanium dioxide Substances 0.000 abstract 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 abstract 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 abstract 1
- 239000002383 tung oil Substances 0.000 abstract 1
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
- C08F8/00—Chemical modification by after-treatment
Landscapes
- Chemical & Material Sciences (AREA)
- General 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)
- Paints Or Removers (AREA)
- Polymerisation Methods In General (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Adhesives Or Adhesive Processes (AREA)
Priority Applications (14)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB22150/63A GB1091521A (en) | 1963-06-04 | 1963-06-04 | Esters of polymers |
| LU46210D LU46210A1 (enrdf_load_html_response) | 1963-06-04 | 1964-06-01 | |
| BE648739A BE648739A (enrdf_load_html_response) | 1963-06-04 | 1964-06-02 | |
| NO153486A NO116299B (enrdf_load_html_response) | 1963-06-04 | 1964-06-02 | |
| ES300516A ES300516A1 (es) | 1963-06-04 | 1964-06-02 | Procedimiento de obtención de un éster de polímero |
| CH721864A CH454465A (de) | 1963-06-04 | 1964-06-03 | Verfahren zur Herstellung eines Polymeresters |
| DE1520153A DE1520153C3 (de) | 1963-06-04 | 1964-06-03 | Verfahren zur Herstellung von polymeren Estern |
| SE6750/64A SE319905B (enrdf_load_html_response) | 1963-06-04 | 1964-06-03 | |
| NL646406256A NL139331B (nl) | 1963-06-04 | 1964-06-03 | Werkwijze voor het bereiden van polymere esters. |
| FI641210A FI45333C (fi) | 1963-06-04 | 1964-06-04 | Menetelmä valmistaa polymeerien estereitä. |
| FR977130A FR1401574A (fr) | 1963-06-04 | 1964-06-04 | Esters de polymères et leur procédé de fabrication |
| DK280964AA DK123416B (da) | 1963-06-04 | 1964-06-04 | Fremgangsmåde til fremstilling af en estergruppeholdig additionspolymer. |
| AT482664A AT268677B (de) | 1963-06-04 | 1964-06-04 | Verfahren zur Herstellung eines Polymeresters |
| MY196939A MY6900039A (enrdf_load_html_response) | 1963-06-04 | 1969-12-31 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB22150/63A GB1091521A (en) | 1963-06-04 | 1963-06-04 | Esters of polymers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1091521A true GB1091521A (en) | 1967-11-15 |
Family
ID=10174735
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB22150/63A Expired GB1091521A (en) | 1963-06-04 | 1963-06-04 | Esters of polymers |
Country Status (14)
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| USRE31309E (en) | 1979-07-18 | 1983-07-12 | E. I. Du Pont De Nemours And Company | High solids ambient temperature curing coatings of acrylic-fatty acid drying oil resins |
| US5185412A (en) * | 1990-01-18 | 1993-02-09 | Rohm And Haas Company | Functionally terminated acrylic acid telomer |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2601023B1 (fr) * | 1986-07-01 | 1989-01-20 | Basf Peintures Encres | Polymere acrylique partiellement esterifie et ses applications notamment pour la preparation de revetements |
-
1963
- 1963-06-04 GB GB22150/63A patent/GB1091521A/en not_active Expired
-
1964
- 1964-06-01 LU LU46210D patent/LU46210A1/xx unknown
- 1964-06-02 BE BE648739A patent/BE648739A/fr unknown
- 1964-06-02 NO NO153486A patent/NO116299B/no unknown
- 1964-06-02 ES ES300516A patent/ES300516A1/es not_active Expired
- 1964-06-03 SE SE6750/64A patent/SE319905B/xx unknown
- 1964-06-03 DE DE1520153A patent/DE1520153C3/de not_active Expired
- 1964-06-03 CH CH721864A patent/CH454465A/de unknown
- 1964-06-03 NL NL646406256A patent/NL139331B/xx unknown
- 1964-06-04 FR FR977130A patent/FR1401574A/fr not_active Expired
- 1964-06-04 FI FI641210A patent/FI45333C/fi active
- 1964-06-04 DK DK280964AA patent/DK123416B/da unknown
- 1964-06-04 AT AT482664A patent/AT268677B/de active
-
1969
- 1969-12-31 MY MY196939A patent/MY6900039A/xx unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| USRE31309E (en) | 1979-07-18 | 1983-07-12 | E. I. Du Pont De Nemours And Company | High solids ambient temperature curing coatings of acrylic-fatty acid drying oil resins |
| US5185412A (en) * | 1990-01-18 | 1993-02-09 | Rohm And Haas Company | Functionally terminated acrylic acid telomer |
Also Published As
| Publication number | Publication date |
|---|---|
| FI45333C (fi) | 1972-05-10 |
| AT268677B (de) | 1969-02-25 |
| LU46210A1 (enrdf_load_html_response) | 1964-08-01 |
| MY6900039A (enrdf_load_html_response) | 1969-12-31 |
| DE1520153A1 (de) | 1969-07-10 |
| NL6406256A (enrdf_load_html_response) | 1964-12-07 |
| FR1401574A (fr) | 1965-06-04 |
| DE1520153C3 (de) | 1974-03-07 |
| SE319905B (enrdf_load_html_response) | 1970-01-26 |
| ES300516A1 (es) | 1964-12-01 |
| NO116299B (enrdf_load_html_response) | 1969-03-03 |
| NL139331B (nl) | 1973-07-16 |
| CH454465A (de) | 1968-04-15 |
| DE1520153B2 (de) | 1973-07-26 |
| DK123416B (da) | 1972-06-19 |
| BE648739A (enrdf_load_html_response) | 1964-12-02 |
| FI45333B (enrdf_load_html_response) | 1972-01-31 |
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