GB672088A - Copolymers of diallyl phthalate and diallyl esters of dimerised unsaturated fatty acids - Google Patents
Copolymers of diallyl phthalate and diallyl esters of dimerised unsaturated fatty acidsInfo
- Publication number
- GB672088A GB672088A GB12483/50A GB1248350A GB672088A GB 672088 A GB672088 A GB 672088A GB 12483/50 A GB12483/50 A GB 12483/50A GB 1248350 A GB1248350 A GB 1248350A GB 672088 A GB672088 A GB 672088A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acids
- dimerized
- heating
- peroxide
- fatty acids
- 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
- 239000004641 Diallyl-phthalate Substances 0.000 title abstract 5
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 title abstract 5
- 235000021122 unsaturated fatty acids Nutrition 0.000 title abstract 5
- 150000004670 unsaturated fatty acids Chemical class 0.000 title abstract 5
- 229920001577 copolymer Polymers 0.000 title abstract 4
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 title abstract 2
- 239000002253 acid Substances 0.000 abstract 16
- 150000007513 acids Chemical class 0.000 abstract 16
- 238000010438 heat treatment Methods 0.000 abstract 8
- 239000000203 mixture Substances 0.000 abstract 5
- 239000003921 oil Substances 0.000 abstract 5
- 235000019198 oils Nutrition 0.000 abstract 5
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 abstract 4
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 4
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 abstract 4
- 239000003054 catalyst Substances 0.000 abstract 4
- 238000004821 distillation Methods 0.000 abstract 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- 238000007334 copolymerization reaction Methods 0.000 abstract 3
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 3
- 239000000194 fatty acid Substances 0.000 abstract 3
- 229930195729 fatty acid Natural products 0.000 abstract 3
- 150000004665 fatty acids Chemical class 0.000 abstract 3
- 150000004702 methyl esters Chemical class 0.000 abstract 3
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 abstract 3
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 abstract 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- 229910015900 BF3 Inorganic materials 0.000 abstract 2
- 239000004342 Benzoyl peroxide Substances 0.000 abstract 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 abstract 2
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 abstract 2
- 241001125048 Sardina Species 0.000 abstract 2
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 abstract 2
- 235000019400 benzoyl peroxide Nutrition 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 abstract 2
- 239000000539 dimer Substances 0.000 abstract 2
- 238000000605 extraction Methods 0.000 abstract 2
- 239000000463 material Substances 0.000 abstract 2
- -1 palmitoleic Chemical class 0.000 abstract 2
- 150000002978 peroxides Chemical class 0.000 abstract 2
- 238000007127 saponification reaction Methods 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 abstract 2
- OYHQOLUKZRVURQ-HZJYTTRNSA-M 9-cis,12-cis-Octadecadienoate Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC([O-])=O OYHQOLUKZRVURQ-HZJYTTRNSA-M 0.000 abstract 1
- 235000017060 Arachis glabrata Nutrition 0.000 abstract 1
- 244000105624 Arachis hypogaea Species 0.000 abstract 1
- 235000010777 Arachis hypogaea Nutrition 0.000 abstract 1
- 235000018262 Arachis monticola Nutrition 0.000 abstract 1
- 241000972773 Aulopiformes Species 0.000 abstract 1
- 244000056139 Brassica cretica Species 0.000 abstract 1
- 235000003351 Brassica cretica Nutrition 0.000 abstract 1
- 240000002791 Brassica napus Species 0.000 abstract 1
- 235000003343 Brassica rupestris Nutrition 0.000 abstract 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 abstract 1
- 241000273930 Brevoortia tyrannus Species 0.000 abstract 1
- 244000020518 Carthamus tinctorius Species 0.000 abstract 1
- 235000003255 Carthamus tinctorius Nutrition 0.000 abstract 1
- 244000146553 Ceiba pentandra Species 0.000 abstract 1
- 235000003301 Ceiba pentandra Nutrition 0.000 abstract 1
- 241000283153 Cetacea Species 0.000 abstract 1
- 241000252203 Clupea harengus Species 0.000 abstract 1
- 235000010469 Glycine max Nutrition 0.000 abstract 1
- 244000068988 Glycine max Species 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 240000007049 Juglans regia Species 0.000 abstract 1
- 235000009496 Juglans regia Nutrition 0.000 abstract 1
- 240000006240 Linum usitatissimum Species 0.000 abstract 1
- 235000004431 Linum usitatissimum Nutrition 0.000 abstract 1
- 235000008753 Papaver somniferum Nutrition 0.000 abstract 1
- 235000010678 Paulownia tomentosa Nutrition 0.000 abstract 1
- 240000002834 Paulownia tomentosa Species 0.000 abstract 1
- 235000004347 Perilla Nutrition 0.000 abstract 1
- 244000124853 Perilla frutescens Species 0.000 abstract 1
- 235000004443 Ricinus communis Nutrition 0.000 abstract 1
- 244000000231 Sesamum indicum Species 0.000 abstract 1
- 235000003434 Sesamum indicum Nutrition 0.000 abstract 1
- 240000008042 Zea mays Species 0.000 abstract 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 abstract 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 abstract 1
- PDAVOLCVHOKLEO-UHFFFAOYSA-N acetyl benzenecarboperoxoate Chemical compound CC(=O)OOC(=O)C1=CC=CC=C1 PDAVOLCVHOKLEO-UHFFFAOYSA-N 0.000 abstract 1
- 238000007605 air drying Methods 0.000 abstract 1
- 125000005907 alkyl ester group Chemical group 0.000 abstract 1
- 235000021342 arachidonic acid Nutrition 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 abstract 1
- 230000005587 bubbling Effects 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 239000001913 cellulose Substances 0.000 abstract 1
- 229920002678 cellulose Polymers 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 239000010941 cobalt Substances 0.000 abstract 1
- 229910017052 cobalt Inorganic materials 0.000 abstract 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 abstract 1
- 235000005822 corn Nutrition 0.000 abstract 1
- 235000012343 cottonseed oil Nutrition 0.000 abstract 1
- 230000032050 esterification Effects 0.000 abstract 1
- 238000005886 esterification reaction Methods 0.000 abstract 1
- 239000010685 fatty oil Substances 0.000 abstract 1
- 235000004426 flaxseed Nutrition 0.000 abstract 1
- 235000013312 flour Nutrition 0.000 abstract 1
- 238000001879 gelation Methods 0.000 abstract 1
- 235000019514 herring Nutrition 0.000 abstract 1
- 239000011133 lead Substances 0.000 abstract 1
- 229940049918 linoleate Drugs 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- KEGIEOGUARJXQU-UHFFFAOYSA-L manganese(2+);naphthalene-1-carboxylate Chemical compound [Mn+2].C1=CC=C2C(C(=O)[O-])=CC=CC2=C1.C1=CC=C2C(C(=O)[O-])=CC=CC2=C1 KEGIEOGUARJXQU-UHFFFAOYSA-L 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 235000010460 mustard Nutrition 0.000 abstract 1
- 235000021290 n-3 DPA Nutrition 0.000 abstract 1
- 125000005474 octanoate group Chemical group 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 235000020232 peanut Nutrition 0.000 abstract 1
- 239000002685 polymerization catalyst Substances 0.000 abstract 1
- 230000001737 promoting effect Effects 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 235000019515 salmon Nutrition 0.000 abstract 1
- 235000019512 sardine Nutrition 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 238000005809 transesterification reaction Methods 0.000 abstract 1
- 235000020234 walnut Nutrition 0.000 abstract 1
- 239000002023 wood 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
- C08F18/00—Homopolymers and 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 an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid
- C08F18/02—Esters of monocarboxylic acids
- C08F18/04—Vinyl esters
- C08F18/08—Vinyl acetate
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US96142A US2564395A (en) | 1949-05-28 | 1949-05-28 | Copolymers of diallyl phthalate and diallyl esters of dimerized unsaturated fatty acids |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB672088A true GB672088A (en) | 1952-05-14 |
Family
ID=22255728
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB12483/50A Expired GB672088A (en) | 1949-05-28 | 1950-05-18 | Copolymers of diallyl phthalate and diallyl esters of dimerised unsaturated fatty acids |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US2564395A (en, 2012) |
| BE (1) | BE495997A (en, 2012) |
| CH (1) | CH284804A (en, 2012) |
| DE (1) | DE818694C (en, 2012) |
| FR (1) | FR1020389A (en, 2012) |
| GB (1) | GB672088A (en, 2012) |
| NL (1) | NL72216C (en, 2012) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT384430B (de) * | 1985-11-27 | 1987-11-10 | Vianova Kunstharz Ag | Verfahren zur herstellung von copolymerisaten |
-
0
- NL NL72216D patent/NL72216C/xx active
- BE BE495997D patent/BE495997A/xx unknown
-
1949
- 1949-05-28 US US96142A patent/US2564395A/en not_active Expired - Lifetime
-
1950
- 1950-05-18 GB GB12483/50A patent/GB672088A/en not_active Expired
- 1950-05-21 DE DEN906A patent/DE818694C/de not_active Expired
- 1950-05-26 CH CH284804D patent/CH284804A/de unknown
- 1950-05-27 FR FR1020389D patent/FR1020389A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| US2564395A (en) | 1951-08-14 |
| FR1020389A (fr) | 1953-02-05 |
| CH284804A (de) | 1952-08-15 |
| BE495997A (en, 2012) | |
| DE818694C (de) | 1951-10-25 |
| NL72216C (en, 2012) |
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