KR101582107B1 - 네오펜틸 글리콜의 제조방법 - Google Patents
네오펜틸 글리콜의 제조방법 Download PDFInfo
- Publication number
- KR101582107B1 KR101582107B1 KR1020107029466A KR20107029466A KR101582107B1 KR 101582107 B1 KR101582107 B1 KR 101582107B1 KR 1020107029466 A KR1020107029466 A KR 1020107029466A KR 20107029466 A KR20107029466 A KR 20107029466A KR 101582107 B1 KR101582107 B1 KR 101582107B1
- Authority
- KR
- South Korea
- Prior art keywords
- hydrogenation
- oxide
- catalyst
- weight
- neopentyl glycol
- 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.)
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- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 title claims abstract description 35
- 238000000034 method Methods 0.000 title abstract description 14
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 58
- 239000003054 catalyst Substances 0.000 claims abstract description 30
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims abstract description 28
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 claims abstract description 24
- 239000007791 liquid phase Substances 0.000 claims abstract description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 22
- JJMOMMLADQPZNY-UHFFFAOYSA-N 3-hydroxy-2,2-dimethylpropanal Chemical compound OCC(C)(C)C=O JJMOMMLADQPZNY-UHFFFAOYSA-N 0.000 claims abstract description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000000203 mixture Substances 0.000 claims description 19
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims description 16
- 150000001299 aldehydes Chemical class 0.000 claims description 15
- 238000006243 chemical reaction Methods 0.000 claims description 14
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 12
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 12
- 239000003085 diluting agent Substances 0.000 claims description 9
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims description 7
- 150000003973 alkyl amines Chemical group 0.000 claims description 7
- 238000010924 continuous production Methods 0.000 claims description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 4
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 3
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 claims description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 2
- 229910052782 aluminium Inorganic materials 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052788 barium Inorganic materials 0.000 claims description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 2
- 229910052791 calcium Inorganic materials 0.000 claims description 2
- 239000011575 calcium Substances 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- 239000011777 magnesium Substances 0.000 claims description 2
- ISRXMEYARGEVIU-UHFFFAOYSA-N n-methyl-n-propan-2-ylpropan-2-amine Chemical compound CC(C)N(C)C(C)C ISRXMEYARGEVIU-UHFFFAOYSA-N 0.000 claims description 2
- 229910052700 potassium Inorganic materials 0.000 claims description 2
- 239000011591 potassium Substances 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 claims description 2
- RKBCYCFRFCNLTO-UHFFFAOYSA-N triisopropylamine Chemical compound CC(C)N(C(C)C)C(C)C RKBCYCFRFCNLTO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- 239000011701 zinc Substances 0.000 claims description 2
- 229910052726 zirconium Inorganic materials 0.000 claims description 2
- 238000011437 continuous method Methods 0.000 claims 1
- GNVRJGIVDSQCOP-UHFFFAOYSA-N n-ethyl-n-methylethanamine Chemical compound CCN(C)CC GNVRJGIVDSQCOP-UHFFFAOYSA-N 0.000 claims 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract description 41
- -1 aliphatic aldehyde Chemical class 0.000 abstract description 10
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 238000002360 preparation method Methods 0.000 abstract description 2
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 239000000047 product Substances 0.000 description 12
- 238000009835 boiling Methods 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 7
- 239000007858 starting material Substances 0.000 description 7
- HSJKGGMUJITCBW-UHFFFAOYSA-N 3-hydroxybutanal Chemical compound CC(O)CC=O HSJKGGMUJITCBW-UHFFFAOYSA-N 0.000 description 6
- 238000006668 aldol addition reaction Methods 0.000 description 6
- 229910052759 nickel Inorganic materials 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 239000008098 formaldehyde solution Substances 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 150000005846 sugar alcohols Polymers 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 3
- 239000007868 Raney catalyst Substances 0.000 description 3
- 229910000564 Raney nickel Inorganic materials 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 150000004675 formic acid derivatives Chemical class 0.000 description 2
- 239000007792 gaseous phase Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 238000006722 reduction reaction Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- HNWHVVWRJAXEEC-UHFFFAOYSA-N (3-hydroxy-2,2-dimethylpropyl) 2-methylpropanoate Chemical compound CC(C)C(=O)OCC(C)(C)CO HNWHVVWRJAXEEC-UHFFFAOYSA-N 0.000 description 1
- SZCWBURCISJFEZ-UHFFFAOYSA-N (3-hydroxy-2,2-dimethylpropyl) 3-hydroxy-2,2-dimethylpropanoate Chemical compound OCC(C)(C)COC(=O)C(C)(C)CO SZCWBURCISJFEZ-UHFFFAOYSA-N 0.000 description 1
- FJJYHTVHBVXEEQ-UHFFFAOYSA-N 2,2-dimethylpropanal Chemical compound CC(C)(C)C=O FJJYHTVHBVXEEQ-UHFFFAOYSA-N 0.000 description 1
- YVAACGXAZGGQSM-UHFFFAOYSA-N 2,2-dimethylpropaneperoxoic acid Chemical compound CC(C)(C)C(=O)OO YVAACGXAZGGQSM-UHFFFAOYSA-N 0.000 description 1
- RDFQSFOGKVZWKF-UHFFFAOYSA-N 3-hydroxy-2,2-dimethylpropanoic acid Chemical group OCC(C)(C)C(O)=O RDFQSFOGKVZWKF-UHFFFAOYSA-N 0.000 description 1
- 238000005705 Cannizzaro reaction Methods 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- VPNWPTNERCWIRN-UHFFFAOYSA-N O.OCC(C)(C)CO Chemical compound O.OCC(C)(C)CO VPNWPTNERCWIRN-UHFFFAOYSA-N 0.000 description 1
- 238000006423 Tishchenko reaction Methods 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000012084 conversion product Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- WMWXXXSCZVGQAR-UHFFFAOYSA-N dialuminum;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3] WMWXXXSCZVGQAR-UHFFFAOYSA-N 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 238000007323 disproportionation reaction Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
- C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
- C07C29/14—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of a —CHO group
- C07C29/141—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of a —CHO group with hydrogen or hydrogen-containing gases
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102008031338A DE102008031338B4 (de) | 2008-07-02 | 2008-07-02 | Verfahren zur Herstellung von Neopentylglykol |
| DE102008031338.6 | 2008-07-02 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20110031164A KR20110031164A (ko) | 2011-03-24 |
| KR101582107B1 true KR101582107B1 (ko) | 2016-01-04 |
Family
ID=41265625
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020107029466A Active KR101582107B1 (ko) | 2008-07-02 | 2009-06-12 | 네오펜틸 글리콜의 제조방법 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US8394998B2 (https=) |
| EP (1) | EP2318342B1 (https=) |
| JP (1) | JP5396470B2 (https=) |
| KR (1) | KR101582107B1 (https=) |
| CN (1) | CN102083776B (https=) |
| BR (1) | BRPI0913920A2 (https=) |
| DE (1) | DE102008031338B4 (https=) |
| PL (1) | PL2318342T3 (https=) |
| TW (1) | TWI367876B (https=) |
| WO (1) | WO2010000382A2 (https=) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101900490B1 (ko) | 2017-09-27 | 2018-09-19 | (주)엔나노텍 | 탄화수소계 발포제와의 혼합성 및 난연성이 우수한 폴리에스터 폴리올의 제조방법 |
| KR20220016976A (ko) * | 2019-06-04 | 2022-02-10 | 오큐 케미칼스 게엠베하 | 라니 코발트 촉매 작용에 의해 알데하이드로부터 디올을 연속적으로 생성하는 방법 |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2012153379A (ru) * | 2010-05-12 | 2014-06-20 | Басф Се | Способ получения неопентилгликоля |
| DE102012021276A1 (de) * | 2012-10-29 | 2014-04-30 | Oxea Gmbh | Kontinuierliches Verfahren zur Herstellung von Neopentylglykol |
| US8710278B1 (en) | 2013-01-31 | 2014-04-29 | Eastman Chemical Company | Process for producing polyols |
| US9056824B2 (en) | 2013-01-31 | 2015-06-16 | Eastman Chemical Company | Preparation of hydroxy aldehydes |
| KR101662875B1 (ko) * | 2013-04-23 | 2016-10-06 | 주식회사 엘지화학 | 네오펜틸글리콜의 제조방법 |
| DE102014100996B4 (de) * | 2014-01-28 | 2018-11-15 | Oxea Gmbh | Verfahren zur Herstellung von Neopentylglykol |
| KR101655973B1 (ko) * | 2014-04-15 | 2016-09-08 | 한화케미칼 주식회사 | 하이드록시피브알데히드의 제조방법 |
| CN105085212A (zh) * | 2014-05-14 | 2015-11-25 | 中国石油化工股份有限公司 | 2,2-二甲基-3-羟基丙醛的制备方法 |
| US10336672B2 (en) * | 2014-08-04 | 2019-07-02 | ClearWaterBay Technology, Inc. | System and method for producing neopentyl glycol |
| WO2016047957A1 (ko) * | 2014-09-25 | 2016-03-31 | (주) 엘지화학 | 고효율의 네오펜틸 글리콜의 제조방법 및 이의 제조장치 |
| KR101757053B1 (ko) | 2014-09-25 | 2017-07-12 | 주식회사 엘지화학 | 고효율의 네오펜틸 글리콜의 제조방법 및 이의 제조장치 |
| KR101856763B1 (ko) * | 2015-05-13 | 2018-05-10 | 한화케미칼 주식회사 | 하이드록시피브알데하이드의 연속 제조 방법 |
| CN105175228B (zh) * | 2015-09-01 | 2018-06-26 | 保定市国秀化工有限责任公司 | 一种钙法新戊二醇制备工艺 |
| DE102019209233A1 (de) | 2018-07-06 | 2020-01-09 | Basf Se | Verfahren zur Herstellung eines β-Hydroxyketons |
| JP2021063019A (ja) * | 2019-10-10 | 2021-04-22 | 昭和電工株式会社 | １，３−ブタンジオールの製造方法 |
| KR102680195B1 (ko) * | 2020-10-16 | 2024-06-28 | 주식회사 엘지화학 | 네오펜틸 글리콜의 제조방법 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7388116B2 (en) | 2006-06-06 | 2008-06-17 | Basf Aktiengesellschaft | Hydrogenation of methylolalkanals |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3644675A1 (de) | 1986-12-30 | 1988-07-14 | Ruhrchemie Ag | Verfahren zur herstellung von 2,2-dimethylpropandiol-(1,3) |
| US4851592A (en) * | 1987-10-27 | 1989-07-25 | Eastman Kodak Company | Triethylamine catalyzed neopentyl glycol production utilizing a gas sparged reactor |
| CN1083413C (zh) | 1996-10-22 | 2002-04-24 | 株式会社Lg化学 | 新戊二醇的连续生产方法 |
| FI108029B (fi) | 1997-12-30 | 2001-11-15 | Neste Oy | Menetelmä neopentyyliglykolin valmistamiseksi |
| US6268539B1 (en) | 1999-10-07 | 2001-07-31 | Nan Ya Plastics Corporation | Manufacturing method of neopentyl glycol |
| DE10317543A1 (de) * | 2003-04-16 | 2004-11-04 | Basf Ag | Verfahren zur Hydrierung von Methylolalkanalen |
-
2008
- 2008-07-02 DE DE102008031338A patent/DE102008031338B4/de not_active Expired - Fee Related
-
2009
- 2009-06-12 BR BRPI0913920A patent/BRPI0913920A2/pt active Search and Examination
- 2009-06-12 JP JP2011515158A patent/JP5396470B2/ja active Active
- 2009-06-12 WO PCT/EP2009/004268 patent/WO2010000382A2/de not_active Ceased
- 2009-06-12 US US12/737,224 patent/US8394998B2/en active Active
- 2009-06-12 EP EP09772082A patent/EP2318342B1/de active Active
- 2009-06-12 CN CN2009801252863A patent/CN102083776B/zh active Active
- 2009-06-12 KR KR1020107029466A patent/KR101582107B1/ko active Active
- 2009-06-12 PL PL09772082T patent/PL2318342T3/pl unknown
- 2009-07-01 TW TW098122165A patent/TWI367876B/zh not_active IP Right Cessation
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7388116B2 (en) | 2006-06-06 | 2008-06-17 | Basf Aktiengesellschaft | Hydrogenation of methylolalkanals |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101900490B1 (ko) | 2017-09-27 | 2018-09-19 | (주)엔나노텍 | 탄화수소계 발포제와의 혼합성 및 난연성이 우수한 폴리에스터 폴리올의 제조방법 |
| KR20220016976A (ko) * | 2019-06-04 | 2022-02-10 | 오큐 케미칼스 게엠베하 | 라니 코발트 촉매 작용에 의해 알데하이드로부터 디올을 연속적으로 생성하는 방법 |
| KR102699199B1 (ko) | 2019-06-04 | 2024-08-27 | 오큐 케미칼스 게엠베하 | 라니 코발트 촉매 작용에 의해 알데하이드로부터 디올을 연속적으로 생성하는 방법 |
| US12122737B2 (en) | 2019-06-04 | 2024-10-22 | Oq Chemicals Gmbh | Method for continuously producing diols from aldehydes by means of Raney cobalt catalysis |
Also Published As
| Publication number | Publication date |
|---|---|
| CN102083776A (zh) | 2011-06-01 |
| DE102008031338A1 (de) | 2010-01-07 |
| JP2011526261A (ja) | 2011-10-06 |
| CN102083776B (zh) | 2013-11-13 |
| PL2318342T3 (pl) | 2013-01-31 |
| TWI367876B (en) | 2012-07-11 |
| JP5396470B2 (ja) | 2014-01-22 |
| WO2010000382A3 (de) | 2010-03-18 |
| BRPI0913920A2 (pt) | 2015-10-20 |
| US8394998B2 (en) | 2013-03-12 |
| DE102008031338B4 (de) | 2012-09-13 |
| TW201002656A (en) | 2010-01-16 |
| US20110098515A1 (en) | 2011-04-28 |
| EP2318342B1 (de) | 2012-08-29 |
| WO2010000382A2 (de) | 2010-01-07 |
| KR20110031164A (ko) | 2011-03-24 |
| EP2318342A2 (de) | 2011-05-11 |
| HK1154233A1 (en) | 2012-04-13 |
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