SE412073B - Sett att samtidigt isomerisera och disproportionera talloljeprodukter genom att upphetta dessa med svavel och jod - Google Patents
Sett att samtidigt isomerisera och disproportionera talloljeprodukter genom att upphetta dessa med svavel och jodInfo
- Publication number
- SE412073B SE412073B SE7314509A SE7314509A SE412073B SE 412073 B SE412073 B SE 412073B SE 7314509 A SE7314509 A SE 7314509A SE 7314509 A SE7314509 A SE 7314509A SE 412073 B SE412073 B SE 412073B
- Authority
- SE
- Sweden
- Prior art keywords
- resin
- acid
- sulfur
- product
- iodine
- Prior art date
Links
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 title claims description 50
- 229910052717 sulfur Inorganic materials 0.000 title claims description 50
- 239000011593 sulfur Substances 0.000 title claims description 50
- 238000010438 heat treatment Methods 0.000 title claims description 3
- 239000011347 resin Substances 0.000 claims description 104
- 229920005989 resin Polymers 0.000 claims description 104
- 150000004665 fatty acids Chemical class 0.000 claims description 60
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 58
- 239000000194 fatty acid Substances 0.000 claims description 58
- 229930195729 fatty acid Natural products 0.000 claims description 58
- 239000000047 product Substances 0.000 claims description 52
- 235000008331 Pinus X rigitaeda Nutrition 0.000 claims description 47
- 235000011613 Pinus brutia Nutrition 0.000 claims description 47
- 241000018646 Pinus brutia Species 0.000 claims description 47
- 239000002253 acid Substances 0.000 claims description 41
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 39
- 229910052740 iodine Inorganic materials 0.000 claims description 39
- 239000011630 iodine Substances 0.000 claims description 39
- 238000006243 chemical reaction Methods 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 24
- RSWGJHLUYNHPMX-UHFFFAOYSA-N 1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid Chemical group C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 22
- 150000007513 acids Chemical class 0.000 claims description 21
- 239000003784 tall oil Substances 0.000 claims description 16
- 238000004821 distillation Methods 0.000 claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- 239000007795 chemical reaction product Substances 0.000 claims description 11
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 9
- 239000010665 pine oil Substances 0.000 claims description 9
- 230000035484 reaction time Effects 0.000 claims description 9
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 claims description 7
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 claims description 7
- MLBYBBUZURKHAW-UHFFFAOYSA-N 4-epi-Palustrinsaeure Natural products CC12CCCC(C)(C(O)=O)C1CCC1=C2CCC(C(C)C)=C1 MLBYBBUZURKHAW-UHFFFAOYSA-N 0.000 claims description 4
- MLBYBBUZURKHAW-MISYRCLQSA-N Palustric acid Chemical compound C([C@@]12C)CC[C@@](C)(C(O)=O)[C@@H]1CCC1=C2CCC(C(C)C)=C1 MLBYBBUZURKHAW-MISYRCLQSA-N 0.000 claims description 4
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 claims description 2
- KGMSWPSAVZAMKR-UHFFFAOYSA-N Me ester-3, 22-Dihydroxy-29-hopanoic acid Natural products C1CCC(C(O)=O)(C)C2C1(C)C1CCC(=C(C)C)C=C1CC2 KGMSWPSAVZAMKR-UHFFFAOYSA-N 0.000 claims 2
- KGMSWPSAVZAMKR-ONCXSQPRSA-N Neoabietic acid Chemical compound [C@H]1([C@](CCC2)(C)C(O)=O)[C@@]2(C)[C@H]2CCC(=C(C)C)C=C2CC1 KGMSWPSAVZAMKR-ONCXSQPRSA-N 0.000 claims 2
- 125000002897 diene group Chemical group 0.000 claims 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 claims 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims 1
- 230000003993 interaction Effects 0.000 claims 1
- 239000002023 wood Substances 0.000 claims 1
- 239000003054 catalyst Substances 0.000 description 24
- 239000000203 mixture Substances 0.000 description 17
- 238000007323 disproportionation reaction Methods 0.000 description 16
- 230000008569 process Effects 0.000 description 15
- 238000006116 polymerization reaction Methods 0.000 description 11
- 239000012467 final product Substances 0.000 description 10
- 238000006317 isomerization reaction Methods 0.000 description 10
- 239000003995 emulsifying agent Substances 0.000 description 9
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 8
- 150000001993 dienes Chemical class 0.000 description 8
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 8
- 229920003051 synthetic elastomer Polymers 0.000 description 8
- 239000003760 tallow Substances 0.000 description 8
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 7
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 7
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 7
- 238000004458 analytical method Methods 0.000 description 7
- 230000008901 benefit Effects 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000007789 gas Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 239000005061 synthetic rubber Substances 0.000 description 7
- 239000005642 Oleic acid Substances 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000003379 elimination reaction Methods 0.000 description 6
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 6
- 235000020777 polyunsaturated fatty acids Nutrition 0.000 description 6
- 235000007173 Abies balsamea Nutrition 0.000 description 5
- 239000004857 Balsam Substances 0.000 description 5
- QUUCYKKMFLJLFS-UHFFFAOYSA-N Dehydroabietan Natural products CC1(C)CCCC2(C)C3=CC=C(C(C)C)C=C3CCC21 QUUCYKKMFLJLFS-UHFFFAOYSA-N 0.000 description 5
- NFWKVWVWBFBAOV-UHFFFAOYSA-N Dehydroabietic acid Natural products OC(=O)C1(C)CCCC2(C)C3=CC=C(C(C)C)C=C3CCC21 NFWKVWVWBFBAOV-UHFFFAOYSA-N 0.000 description 5
- 244000018716 Impatiens biflora Species 0.000 description 5
- 239000003513 alkali Substances 0.000 description 5
- 238000004061 bleaching Methods 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- NFWKVWVWBFBAOV-MISYRCLQSA-N dehydroabietic acid Chemical compound OC(=O)[C@]1(C)CCC[C@]2(C)C3=CC=C(C(C)C)C=C3CC[C@H]21 NFWKVWVWBFBAOV-MISYRCLQSA-N 0.000 description 5
- 229940118781 dehydroabietic acid Drugs 0.000 description 5
- 230000008030 elimination Effects 0.000 description 5
- 238000004817 gas chromatography Methods 0.000 description 5
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 4
- 239000000470 constituent Substances 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 4
- 230000009965 odorless effect Effects 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- HXQHFNIKBKZGRP-UHFFFAOYSA-N Ranuncelin-saeure-methylester Natural products CCCCCC=CCC=CCCC=CCCCC(O)=O HXQHFNIKBKZGRP-UHFFFAOYSA-N 0.000 description 3
- 240000006365 Vitis vinifera Species 0.000 description 3
- 235000014787 Vitis vinifera Nutrition 0.000 description 3
- 230000009471 action Effects 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 3
- 238000006114 decarboxylation reaction Methods 0.000 description 3
- 239000003292 glue Substances 0.000 description 3
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 3
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 3
- DFJAXEWDHVOILU-UHFFFAOYSA-N (5Z,9E)-5,9-Octadecadienoic acid Natural products CCCCCCCCC=CCCC=CCCCC(O)=O DFJAXEWDHVOILU-UHFFFAOYSA-N 0.000 description 2
- 238000005698 Diels-Alder reaction Methods 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- 238000006471 dimerization reaction Methods 0.000 description 2
- VYFYYTLLBUKUHU-UHFFFAOYSA-N dopamine Chemical compound NCCC1=CC=C(O)C(O)=C1 VYFYYTLLBUKUHU-UHFFFAOYSA-N 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- 238000011835 investigation Methods 0.000 description 2
- 235000020778 linoleic acid Nutrition 0.000 description 2
- 150000004702 methyl esters Chemical class 0.000 description 2
- 150000002889 oleic acids Chemical class 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 238000007127 saponification reaction Methods 0.000 description 2
- 235000003441 saturated fatty acids Nutrition 0.000 description 2
- 150000004671 saturated fatty acids Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- SFLMUHDGSQZDOW-FAOXUISGSA-N coniferin Chemical compound COC1=CC(\C=C\CO)=CC=C1O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 SFLMUHDGSQZDOW-FAOXUISGSA-N 0.000 description 1
- SFLMUHDGSQZDOW-IBEHDNSVSA-N coniferoside Natural products COC1=CC(C=CCO)=CC=C1O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 SFLMUHDGSQZDOW-IBEHDNSVSA-N 0.000 description 1
- -1 diene fatty acid Chemical class 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 229960003638 dopamine Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- ZQPPMHVWECSIRJ-MDZDMXLPSA-N elaidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(O)=O ZQPPMHVWECSIRJ-MDZDMXLPSA-N 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000004438 eyesight Effects 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000009916 joint effect Effects 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C3/00—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
- C11C3/14—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by isomerisation
-
- 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
- C08F36/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F36/02—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F36/04—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fats And Perfumes (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FI298472A FI49597C (fi) | 1972-10-27 | 1972-10-27 | Tapa disproportionoidun mäntyhartsin valmistamiseksi. |
| FI731865A FI50966C (fi) | 1973-06-08 | 1973-06-08 | Tapa isomeroidun mäntyrasvahapon valmistamiseksi |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SE412073B true SE412073B (sv) | 1980-02-18 |
Family
ID=26156533
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE7314509A SE412073B (sv) | 1972-10-27 | 1973-10-25 | Sett att samtidigt isomerisera och disproportionera talloljeprodukter genom att upphetta dessa med svavel och jod |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US3943118A (en, 2012) |
| JP (1) | JPS5825704B2 (en, 2012) |
| AT (1) | AT330933B (en, 2012) |
| BR (1) | BR7308413D0 (en, 2012) |
| CH (1) | CH588549A5 (en, 2012) |
| CS (1) | CS186777B2 (en, 2012) |
| DD (1) | DD108734A5 (en, 2012) |
| DE (1) | DE2352498A1 (en, 2012) |
| ES (1) | ES419896A1 (en, 2012) |
| FR (1) | FR2204679B1 (en, 2012) |
| GB (1) | GB1444430A (en, 2012) |
| IT (1) | IT999014B (en, 2012) |
| NL (1) | NL7314840A (en, 2012) |
| NO (1) | NO140798C (en, 2012) |
| SE (1) | SE412073B (en, 2012) |
| SU (1) | SU511026A3 (en, 2012) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4271066A (en) * | 1979-11-05 | 1981-06-02 | Arakawa Kagaku Kogyo Kabushiki Kaisha | Process for disproportionating rosin, poly-unsaturated fatty acids and mixtures thereof |
| GB8506023D0 (en) * | 1985-03-08 | 1985-04-11 | Enichem Elastomers Ltd | Disproportionation of unsaturated acids |
| JPH08209070A (ja) * | 1995-02-08 | 1996-08-13 | Harima Chem Inc | 淡色なトール油ロジンエステルの製造法 |
| RU2144527C1 (ru) * | 1997-04-24 | 2000-01-20 | Товарищество с ограниченной ответственностью "Лесма" | Способ диспропорционирования смесей жирных и смоляных кислот |
| WO2000050528A1 (en) * | 1999-02-25 | 2000-08-31 | Arizona Chemical Company | Method for isolating oleic acid and producing lineloic dimer/trimer acids via selective reactivity |
| US6835324B1 (en) | 1999-02-25 | 2004-12-28 | Arizona Chemical Company | Method for isolating oleic acid and producing lineloic dimer/trimer acids via selective reactivity |
| RU2181741C1 (ru) * | 2001-07-17 | 2002-04-27 | Открытое акционерное общество "Оргсинтез" | Способ диспропорционирования талловой канифоли |
| CA2599980A1 (en) * | 2005-02-09 | 2006-08-17 | Albemarle Corporation | Method of producing disproportionated rosin |
| US20110213120A1 (en) * | 2010-03-01 | 2011-09-01 | Arizona Chemical Company | Rosin esters for non-woven applications, methods of making and using and products therefrom |
| RU2535703C2 (ru) * | 2012-09-25 | 2014-12-20 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Московский государственный университет технологий и управления имени К.Г. Разумовского" | Способ диспропорционирования талловой канифоли |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1957788A (en) * | 1929-08-22 | 1934-05-08 | Hercules Powder Co Ltd | Method of refining rosin |
| US2717838A (en) * | 1951-07-11 | 1955-09-13 | American Cyanamid Co | Stabilized tall oil rosin and dry sizes prepared therefrom |
| US2794017A (en) * | 1953-05-14 | 1957-05-28 | Heyden Newport Chemical Corp | Method of processing tall oil and products produced thereby |
| US3157629A (en) * | 1959-02-13 | 1964-11-17 | West Virginia Pulp & Paper Co | Treatment of tall oil fatty acids |
| DE1205530B (de) * | 1963-10-07 | 1965-11-25 | Anciens Etablissements Granel | Verfahren zur Gewinnung von mehr als 30 Gewichtsprozent Dehydroabietinsaeure enthaltenden Gemischen |
| US3277072A (en) * | 1964-07-13 | 1966-10-04 | West Virginia Pulp & Paper Co | Fluid rosin |
| US3377334A (en) * | 1966-09-16 | 1968-04-09 | Arizona Chem | Disproportionation of rosin |
| US3528959A (en) * | 1967-12-26 | 1970-09-15 | Westvaco Corp | Modified tall oil emulsifiers |
| US3860569A (en) * | 1972-01-07 | 1975-01-14 | Westvaco Corp | Treatment of tall oil fatty acids |
-
1973
- 1973-10-19 DE DE19732352498 patent/DE2352498A1/de active Granted
- 1973-10-23 CH CH1494173A patent/CH588549A5/xx not_active IP Right Cessation
- 1973-10-23 NO NO4106/73A patent/NO140798C/no unknown
- 1973-10-24 GB GB4961273A patent/GB1444430A/en not_active Expired
- 1973-10-24 ES ES419896A patent/ES419896A1/es not_active Expired
- 1973-10-25 SE SE7314509A patent/SE412073B/sv unknown
- 1973-10-25 AT AT905073A patent/AT330933B/de not_active IP Right Cessation
- 1973-10-26 CS CS7300007394A patent/CS186777B2/cs unknown
- 1973-10-26 BR BR8413/73A patent/BR7308413D0/pt unknown
- 1973-10-26 DD DD174311A patent/DD108734A5/xx unknown
- 1973-10-26 IT IT30639/73A patent/IT999014B/it active
- 1973-10-26 SU SU1967883A patent/SU511026A3/ru active
- 1973-10-26 US US05/410,019 patent/US3943118A/en not_active Expired - Lifetime
- 1973-10-26 FR FR7338314A patent/FR2204679B1/fr not_active Expired
- 1973-10-27 JP JP48121166A patent/JPS5825704B2/ja not_active Expired
- 1973-10-29 NL NL7314840A patent/NL7314840A/xx active Search and Examination
Also Published As
| Publication number | Publication date |
|---|---|
| CH588549A5 (en, 2012) | 1977-06-15 |
| DE2352498A1 (de) | 1974-06-06 |
| DE2352498C2 (en, 2012) | 1989-04-27 |
| US3943118A (en) | 1976-03-09 |
| AU6186773A (en) | 1975-05-01 |
| NL7314840A (en, 2012) | 1974-05-01 |
| BR7308413D0 (pt) | 1974-08-29 |
| JPS4997805A (en, 2012) | 1974-09-17 |
| CS186777B2 (en) | 1978-12-29 |
| SU511026A3 (ru) | 1976-04-15 |
| FR2204679A1 (en, 2012) | 1974-05-24 |
| JPS5825704B2 (ja) | 1983-05-28 |
| FR2204679B1 (en, 2012) | 1977-05-27 |
| ES419896A1 (es) | 1976-08-01 |
| NO140798C (no) | 1979-11-14 |
| NO140798B (no) | 1979-08-06 |
| DD108734A5 (en, 2012) | 1974-10-05 |
| AT330933B (de) | 1976-07-26 |
| ATA905073A (de) | 1975-10-15 |
| GB1444430A (en) | 1976-07-28 |
| IT999014B (it) | 1976-02-20 |
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