BE706968A - - Google Patents
Info
- Publication number
- BE706968A BE706968A BE706968DA BE706968A BE 706968 A BE706968 A BE 706968A BE 706968D A BE706968D A BE 706968DA BE 706968 A BE706968 A BE 706968A
- Authority
- BE
- Belgium
- Prior art keywords
- sep
- process according
- sucrose
- minutes
- total weight
- Prior art date
Links
- 239000000203 mixture Substances 0.000 claims description 32
- 239000002518 antifoaming agent Substances 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 22
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims description 14
- 229930006000 Sucrose Natural products 0.000 claims description 13
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 12
- 229930195729 fatty acid Natural products 0.000 claims description 12
- 239000000194 fatty acid Substances 0.000 claims description 12
- 239000005720 sucrose Substances 0.000 claims description 12
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 10
- 230000003254 anti-foaming effect Effects 0.000 claims description 8
- 150000001720 carbohydrates Chemical class 0.000 claims description 8
- 235000014633 carbohydrates Nutrition 0.000 claims description 8
- 150000004665 fatty acids Chemical class 0.000 claims description 7
- 229930195733 hydrocarbon Natural products 0.000 claims description 7
- 150000002430 hydrocarbons Chemical class 0.000 claims description 7
- 235000013379 molasses Nutrition 0.000 claims description 6
- 239000003921 oil Substances 0.000 claims description 6
- 125000002947 alkylene group Chemical group 0.000 claims description 5
- -1 fatty acid esters Chemical class 0.000 claims description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 4
- 235000019198 oils Nutrition 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 claims description 3
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 claims description 3
- 239000003054 catalyst Substances 0.000 claims description 3
- 125000004494 ethyl ester group Chemical group 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 239000010865 sewage Substances 0.000 claims description 3
- 235000013311 vegetables Nutrition 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 239000000839 emulsion Substances 0.000 claims description 2
- 235000019197 fats Nutrition 0.000 claims description 2
- 235000011389 fruit/vegetable juice Nutrition 0.000 claims description 2
- 239000013067 intermediate product Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000000463 material Substances 0.000 claims description 2
- 238000007670 refining Methods 0.000 claims description 2
- 235000020357 syrup Nutrition 0.000 claims description 2
- 239000006188 syrup Substances 0.000 claims description 2
- 238000005809 transesterification reaction Methods 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 claims 1
- 239000003925 fat Substances 0.000 claims 1
- 150000004677 hydrates Chemical class 0.000 claims 1
- 235000015112 vegetable and seed oil Nutrition 0.000 claims 1
- 235000019871 vegetable fat Nutrition 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000006260 foam Substances 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 239000003760 tallow Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 235000019482 Palm oil Nutrition 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 239000002540 palm oil Substances 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000014121 butter Nutrition 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 230000002478 diastatic effect Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000010771 distillate fuel oil Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 231100000956 nontoxicity Toxicity 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
- 239000002994 raw material Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
- C07H13/02—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids
- C07H13/04—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids having the esterifying carboxyl radicals attached to acyclic carbon atoms
- C07H13/06—Fatty acids
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D19/00—Degasification of liquids
- B01D19/02—Foam dispersion or prevention
- B01D19/04—Foam dispersion or prevention by addition of chemical substances
- B01D19/0404—Foam dispersion or prevention by addition of chemical substances characterised by the nature of the chemical substance
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
- C07H13/02—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids
- C07H13/08—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids having the esterifying carboxyl radicals directly attached to carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/02—Acyclic radicals, not substituted by cyclic structures
- C07H15/04—Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical
- C07H15/06—Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical being a hydroxyalkyl group esterified by a fatty acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/02—Acyclic radicals, not substituted by cyclic structures
- C07H15/04—Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical
- C07H15/08—Polyoxyalkylene derivatives
-
- 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
-
- 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
- C11C3/04—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fats or fatty oils
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Toxicology (AREA)
- Dispersion Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Saccharide Compounds (AREA)
- Fats And Perfumes (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU49607 | 1965-10-08 | ||
| LU50954A LU50954A1 (OSRAM) | 1966-04-22 | 1966-04-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE706968A true BE706968A (OSRAM) | 1968-04-01 |
Family
ID=26639961
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE687223D BE687223A (OSRAM) | 1965-10-08 | 1966-09-22 | |
| BE706968D BE706968A (OSRAM) | 1965-10-08 | 1967-11-23 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE687223D BE687223A (OSRAM) | 1965-10-08 | 1966-09-22 |
Country Status (6)
| Country | Link |
|---|---|
| BE (2) | BE687223A (OSRAM) |
| ES (1) | ES331611A1 (OSRAM) |
| FR (1) | FR1515012A (OSRAM) |
| GB (2) | GB1160144A (OSRAM) |
| LU (1) | LU49607A1 (OSRAM) |
| NL (1) | NL6613998A (OSRAM) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH09242A (ja) * | 1995-06-23 | 1997-01-07 | Kao Corp | 発酵用消泡剤及びこれを用いた発酵生産方法 |
| EP2439187A1 (en) * | 2008-12-19 | 2012-04-11 | Cognis IP Management GmbH | Alkoxylated carbohydrate esters and their use |
| CN111821722B (zh) * | 2019-04-22 | 2022-03-29 | 中国石油天然气股份有限公司 | 一种用于气井泡沫排水采气的纳米固体消泡剂及其制备方法 |
-
1965
- 1965-10-08 LU LU49607D patent/LU49607A1/xx unknown
-
1966
- 1966-09-19 GB GB4167466A patent/GB1160144A/en not_active Expired
- 1966-09-22 BE BE687223D patent/BE687223A/xx unknown
- 1966-09-26 ES ES0331611A patent/ES331611A1/es not_active Expired
- 1966-09-29 FR FR78179A patent/FR1515012A/fr not_active Expired
- 1966-10-04 NL NL6613998A patent/NL6613998A/xx unknown
-
1967
- 1967-11-23 BE BE706968D patent/BE706968A/fr unknown
- 1967-11-30 GB GB5457367A patent/GB1216987A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| NL6613998A (OSRAM) | 1967-04-10 |
| GB1216987A (en) | 1970-12-23 |
| BE687223A (OSRAM) | 1967-03-22 |
| LU49607A1 (OSRAM) | 1967-04-08 |
| GB1160144A (en) | 1969-07-30 |
| FR1515012A (fr) | 1968-03-01 |
| ES331611A1 (es) | 1967-07-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3586715A (en) | Unsaturated carboxylic salt materials and derivatives thereof | |
| US20060041156A1 (en) | Methods of preparing hydroxy functional vegetable oils | |
| US8350070B2 (en) | Methods of preparing hydroxy functional vegetable oils | |
| EP0582507B1 (fr) | Méthode pour réduire la tendance à l'agglomération des hydrates dans des effluents de production | |
| JPH04230356A (ja) | 第二アルキル硫酸塩含有界面活性剤組成物の製造方法 | |
| EP1126011A2 (en) | Process for producing fatty acid esters and fuels comprising fatty acid ester | |
| CN1025745C (zh) | 燃料组合物 | |
| FR2580664A1 (fr) | Agent tensio-actif liquide biodegradable et son utilisation | |
| CA2393403C (en) | Method for commercial preparation of linoleic acid | |
| JP2023078348A (ja) | 高級第２級アルコールアルコキシレート前駆体、高級第２級アルコールアルコキシレート付加物および高級第２級アルキルエーテル硫酸エステル塩並びにその製造方法 | |
| US3429136A (en) | Process for preparing hydroxy sulfonate esters | |
| BE706968A (OSRAM) | ||
| FR2527625A1 (fr) | Composition a base de fluorochlorohydrocarbure, d'ester phosphorique et d'acide carboxylique | |
| US6822104B2 (en) | Method for commercial preparation of preferred isomeric forms of ester free conjugated fatty acids with solvents systems containing polyether alcohol solvents | |
| EP1053781B1 (fr) | Compositions utilisables comme agents de surface émulsifiants et dispersants, leur préparation et leurs utilisations | |
| FR2780732A1 (fr) | Compositions detergentes non moussantes pour milieux alcalins concentres | |
| EP1802565B1 (en) | Process for preparing hydroxy functional vegetable oils | |
| US3742030A (en) | Unsaturated carboxylic salt materials and derivatives thereof | |
| RU2680963C1 (ru) | Присадка к дизельному топливу комплексного действия и способ ее получения | |
| US4217289A (en) | Process for purification of the alkali metal salt of sulfonated unsaturated aliphatic carboxylic acid | |
| US2313719A (en) | Manufacture of organic sulphitation products | |
| CN110240956A (zh) | 一种脂肪酸酯型柴油抗磨剂的制备方法 | |
| SU1031972A1 (ru) | Блоксополимер на основе изобутилена и окиси этилена в качестве деэмульгатора дл нефти | |
| US10822572B2 (en) | Process of producing basic biosolvents using heterogeneous catalysts and obtained basic biosolvents by this process | |
| Ahmadova et al. | SYNTHESIS AND PROPERTIES OF SURFACE-ACTIVE COOLIGOMERS BASED ON C3-EPOXIDES AND LAURIC ACID |