CN115521218B - 一种氨基酸表面活性剂原料的制备方法 - Google Patents
一种氨基酸表面活性剂原料的制备方法 Download PDFInfo
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- CN115521218B CN115521218B CN202210885540.7A CN202210885540A CN115521218B CN 115521218 B CN115521218 B CN 115521218B CN 202210885540 A CN202210885540 A CN 202210885540A CN 115521218 B CN115521218 B CN 115521218B
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- amino
- reaction
- amino acid
- mixed gas
- alumina catalyst
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- 239000004094 surface-active agent Substances 0.000 title claims abstract description 28
- 150000001413 amino acids Chemical class 0.000 title claims abstract description 25
- 238000002360 preparation method Methods 0.000 title claims abstract description 23
- 239000002994 raw material Substances 0.000 title claims abstract description 20
- -1 2-amino fatty alcohol Chemical class 0.000 claims abstract description 42
- 238000006243 chemical reaction Methods 0.000 claims abstract description 41
- 239000003054 catalyst Substances 0.000 claims abstract description 27
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 26
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 22
- 239000007789 gas Substances 0.000 claims abstract description 22
- 239000001301 oxygen Substances 0.000 claims abstract description 22
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 22
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 19
- 229930195729 fatty acid Natural products 0.000 claims abstract description 19
- 239000000194 fatty acid Substances 0.000 claims abstract description 19
- 238000002309 gasification Methods 0.000 claims abstract description 17
- 238000002156 mixing Methods 0.000 claims abstract description 14
- 239000007788 liquid Substances 0.000 claims abstract description 13
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 10
- 238000002347 injection Methods 0.000 claims abstract description 10
- 239000007924 injection Substances 0.000 claims abstract description 10
- 238000005086 pumping Methods 0.000 claims abstract description 8
- 238000000034 method Methods 0.000 claims abstract description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 36
- 239000008367 deionised water Substances 0.000 claims description 22
- 229910021641 deionized water Inorganic materials 0.000 claims description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 22
- 238000002425 crystallisation Methods 0.000 claims description 18
- 230000008025 crystallization Effects 0.000 claims description 18
- 238000005406 washing Methods 0.000 claims description 16
- 238000001035 drying Methods 0.000 claims description 13
- 239000000047 product Substances 0.000 claims description 13
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 12
- 238000001914 filtration Methods 0.000 claims description 12
- 239000008103 glucose Substances 0.000 claims description 12
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 claims description 12
- 239000001509 sodium citrate Substances 0.000 claims description 12
- 238000003756 stirring Methods 0.000 claims description 11
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 9
- 229910052782 aluminium Inorganic materials 0.000 claims description 9
- 239000000706 filtrate Substances 0.000 claims description 9
- 238000001027 hydrothermal synthesis Methods 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 claims description 5
- JPUHCPXFQIXLMW-UHFFFAOYSA-N aluminium triethoxide Chemical compound CCO[Al](OCC)OCC JPUHCPXFQIXLMW-UHFFFAOYSA-N 0.000 claims description 5
- 150000002191 fatty alcohols Chemical class 0.000 claims description 4
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims description 3
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 claims description 2
- 239000000463 material Substances 0.000 claims 4
- 238000004519 manufacturing process Methods 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 238000003889 chemical engineering Methods 0.000 abstract description 2
- 239000012847 fine chemical Substances 0.000 abstract description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 6
- DHDQQXZPXPREBK-UHFFFAOYSA-N 2-aminooctadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCC(N)CO DHDQQXZPXPREBK-UHFFFAOYSA-N 0.000 description 4
- QNAYBMKLOCPYGJ-UHFFFAOYSA-N Alanine Chemical compound CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 description 4
- QWCKQJZIFLGMSD-UHFFFAOYSA-N alpha-aminobutyric acid Chemical group CCC(N)C(O)=O QWCKQJZIFLGMSD-UHFFFAOYSA-N 0.000 description 4
- JCBPETKZIGVZRE-UHFFFAOYSA-N 2-aminobutan-1-ol Chemical compound CCC(N)CO JCBPETKZIGVZRE-UHFFFAOYSA-N 0.000 description 3
- VFAALMIZIKQCCB-UHFFFAOYSA-N 2-aminododecan-1-ol Chemical compound CCCCCCCCCCC(N)CO VFAALMIZIKQCCB-UHFFFAOYSA-N 0.000 description 3
- DPEOTCPCYHSVTC-UHFFFAOYSA-N 2-aminohexan-1-ol Chemical compound CCCCC(N)CO DPEOTCPCYHSVTC-UHFFFAOYSA-N 0.000 description 3
- LRQKBLKVPFOOQJ-UHFFFAOYSA-N 2-aminohexanoic acid Chemical group CCCCC(N)C(O)=O LRQKBLKVPFOOQJ-UHFFFAOYSA-N 0.000 description 3
- DGXJAZWKEXOLBW-UHFFFAOYSA-N 2-aminooctan-1-ol Chemical compound CCCCCCC(N)CO DGXJAZWKEXOLBW-UHFFFAOYSA-N 0.000 description 3
- BKMMTJMQCTUHRP-UHFFFAOYSA-N 2-aminopropan-1-ol Chemical compound CC(N)CO BKMMTJMQCTUHRP-UHFFFAOYSA-N 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- XRKBQVGBWJWJJJ-UHFFFAOYSA-N 2-aminooctadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(N)C(O)=O XRKBQVGBWJWJJJ-UHFFFAOYSA-N 0.000 description 2
- QUBNFZFTFXTLKH-UHFFFAOYSA-N 2-aminododecanoic acid Chemical group CCCCCCCCCCC(N)C(O)=O QUBNFZFTFXTLKH-UHFFFAOYSA-N 0.000 description 1
- AKVBCGQVQXPRLD-UHFFFAOYSA-N 2-aminooctanoic acid Chemical compound CCCCCCC(N)C(O)=O AKVBCGQVQXPRLD-UHFFFAOYSA-N 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 230000000202 analgesic effect Effects 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 239000000551 dentifrice Substances 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000002324 mouth wash Substances 0.000 description 1
- 229940051866 mouthwash Drugs 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 239000000606 toothpaste Substances 0.000 description 1
- 229940034610 toothpaste Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C227/02—Formation of carboxyl groups in compounds containing amino groups, e.g. by oxidation of amino alcohols
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/02—Boron or aluminium; Oxides or hydroxides thereof
- B01J21/04—Alumina
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/584—Recycling of catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims (5)
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CN202210885540.7A CN115521218B (zh) | 2022-07-26 | 2022-07-26 | 一种氨基酸表面活性剂原料的制备方法 |
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CN115521218A CN115521218A (zh) | 2022-12-27 |
CN115521218B true CN115521218B (zh) | 2023-08-22 |
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Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0326934A1 (de) * | 1988-02-02 | 1989-08-09 | BASF Aktiengesellschaft | Verfahren zur Reduktion reduzierbarer Verbindungen |
JPH05140056A (ja) * | 1991-11-25 | 1993-06-08 | Kao Corp | Dl−セリンの製造方法 |
JP2000063338A (ja) * | 1998-08-20 | 2000-02-29 | Mitsui Chemicals Inc | アミノカルボン酸塩の製造方法 |
CN102443608A (zh) * | 2010-10-12 | 2012-05-09 | 中国石油化工股份有限公司 | 一种利用微生物发酵生产1,3-丙二醇的方法 |
CN102500408A (zh) * | 2011-10-20 | 2012-06-20 | 内蒙古民族大学 | 微孔-介孔催化材料及其制备方法 |
CN102822146A (zh) * | 2010-04-06 | 2012-12-12 | 住友化学株式会社 | 用于制备含硫氨基酸的方法 |
CN103214373A (zh) * | 2013-05-06 | 2013-07-24 | 山东大学 | 一种碳酸甲乙酯的合成方法 |
CN105728019A (zh) * | 2016-03-17 | 2016-07-06 | 中国天辰工程有限公司 | 一种具有介微孔的zsm-5分子筛的制备方法及应用 |
CN108160101A (zh) * | 2018-01-02 | 2018-06-15 | 中国矿业大学 | 一种甲醇制烯烃催化剂及其制备方法和应用 |
CN109535846A (zh) * | 2018-12-21 | 2019-03-29 | 湖北工业大学 | 一种基于羟基磷灰石纳米晶荧光隐形墨水的制备方法 |
CN112778144A (zh) * | 2019-11-05 | 2021-05-11 | 中国科学院大连化学物理研究所 | 甘氨酸的制备方法 |
WO2022062801A1 (zh) * | 2020-09-24 | 2022-03-31 | 南京大学 | 一种具有缺电子Cu中心的类芬顿催化材料及其制备方法和应用 |
-
2022
- 2022-07-26 CN CN202210885540.7A patent/CN115521218B/zh active Active
Patent Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0326934A1 (de) * | 1988-02-02 | 1989-08-09 | BASF Aktiengesellschaft | Verfahren zur Reduktion reduzierbarer Verbindungen |
JPH05140056A (ja) * | 1991-11-25 | 1993-06-08 | Kao Corp | Dl−セリンの製造方法 |
JP2000063338A (ja) * | 1998-08-20 | 2000-02-29 | Mitsui Chemicals Inc | アミノカルボン酸塩の製造方法 |
CN102822146A (zh) * | 2010-04-06 | 2012-12-12 | 住友化学株式会社 | 用于制备含硫氨基酸的方法 |
CN102443608A (zh) * | 2010-10-12 | 2012-05-09 | 中国石油化工股份有限公司 | 一种利用微生物发酵生产1,3-丙二醇的方法 |
CN102500408A (zh) * | 2011-10-20 | 2012-06-20 | 内蒙古民族大学 | 微孔-介孔催化材料及其制备方法 |
CN103214373A (zh) * | 2013-05-06 | 2013-07-24 | 山东大学 | 一种碳酸甲乙酯的合成方法 |
CN105728019A (zh) * | 2016-03-17 | 2016-07-06 | 中国天辰工程有限公司 | 一种具有介微孔的zsm-5分子筛的制备方法及应用 |
CN108160101A (zh) * | 2018-01-02 | 2018-06-15 | 中国矿业大学 | 一种甲醇制烯烃催化剂及其制备方法和应用 |
CN109535846A (zh) * | 2018-12-21 | 2019-03-29 | 湖北工业大学 | 一种基于羟基磷灰石纳米晶荧光隐形墨水的制备方法 |
CN112778144A (zh) * | 2019-11-05 | 2021-05-11 | 中国科学院大连化学物理研究所 | 甘氨酸的制备方法 |
WO2022062801A1 (zh) * | 2020-09-24 | 2022-03-31 | 南京大学 | 一种具有缺电子Cu中心的类芬顿催化材料及其制备方法和应用 |
Non-Patent Citations (1)
Title |
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Peng Qian等.Electrocatalytic Intermolecular C(sp3)−H/N−H Coupling of Methyl N‐Heteroaromatics with Amines and Amino Acids: Access to Imidazo-Fused N‐Heterocycles.《Org. Lett.》.2018,第20卷(第20期),6359-6363,尤其是scheme3. * |
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Effective date of registration: 20231220 Address after: Room 401, No. 2403 Chuangye Avenue, Huangpu District, Guangzhou City, Guangdong Province, 510000 Patentee after: Guangzhou Yingke Chemical Technology Co.,Ltd. Address before: 230000 Room 203, building 2, phase I, e-commerce Park, Jinggang Road, Shushan Economic Development Zone, Hefei City, Anhui Province Patentee before: Hefei Jiuzhou Longteng scientific and technological achievement transformation Co.,Ltd. Effective date of registration: 20231220 Address after: 230000 Room 203, building 2, phase I, e-commerce Park, Jinggang Road, Shushan Economic Development Zone, Hefei City, Anhui Province Patentee after: Hefei Jiuzhou Longteng scientific and technological achievement transformation Co.,Ltd. Address before: 224051 middle road of hope Avenue, Yancheng City, Jiangsu Province, No. 1 Patentee before: YANCHENG INSTITUTE OF TECHNOLOGY |