NZ586736A - Process for the production of 1,2-propanediol - Google Patents
Process for the production of 1,2-propanediolInfo
- Publication number
- NZ586736A NZ586736A NZ586736A NZ58673608A NZ586736A NZ 586736 A NZ586736 A NZ 586736A NZ 586736 A NZ586736 A NZ 586736A NZ 58673608 A NZ58673608 A NZ 58673608A NZ 586736 A NZ586736 A NZ 586736A
- Authority
- NZ
- New Zealand
- Prior art keywords
- glycerol
- product stream
- hydrogenation
- crude product
- stream
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 67
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 title claims abstract description 18
- 235000013772 propylene glycol Nutrition 0.000 title claims abstract description 16
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 title claims abstract description 15
- 238000004519 manufacturing process Methods 0.000 title description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 152
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 40
- 239000012043 crude product Substances 0.000 claims abstract description 27
- XLSMFKSTNGKWQX-UHFFFAOYSA-N hydroxyacetone Chemical compound CC(=O)CO XLSMFKSTNGKWQX-UHFFFAOYSA-N 0.000 claims abstract description 25
- 239000007789 gas Substances 0.000 claims abstract description 24
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 23
- 239000012071 phase Substances 0.000 claims abstract description 22
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 21
- 239000001257 hydrogen Substances 0.000 claims abstract description 21
- 239000007791 liquid phase Substances 0.000 claims abstract description 11
- 239000012535 impurity Substances 0.000 claims abstract description 8
- 238000004817 gas chromatography Methods 0.000 claims abstract description 4
- 239000002638 heterogeneous catalyst Substances 0.000 claims abstract description 4
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000000047 product Substances 0.000 claims description 25
- 238000006243 chemical reaction Methods 0.000 claims description 24
- 239000003054 catalyst Substances 0.000 claims description 21
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical group [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 12
- 239000000463 material Substances 0.000 claims description 11
- 239000013067 intermediate product Substances 0.000 claims description 9
- 238000009834 vaporization Methods 0.000 claims description 9
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 6
- 229910052759 nickel Inorganic materials 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims description 4
- 239000010949 copper Substances 0.000 claims description 4
- 229910017052 cobalt Inorganic materials 0.000 claims description 3
- 239000010941 cobalt Substances 0.000 claims description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 3
- 230000018044 dehydration Effects 0.000 claims description 3
- 238000006297 dehydration reaction Methods 0.000 claims description 3
- 239000012263 liquid product Substances 0.000 claims description 3
- 229910052707 ruthenium Inorganic materials 0.000 claims description 3
- 235000011187 glycerol Nutrition 0.000 description 39
- 238000004821 distillation Methods 0.000 description 12
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 6
- 239000006227 byproduct Substances 0.000 description 4
- 150000004862 dioxolanes Chemical class 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical class CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 3
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 235000014593 oils and fats Nutrition 0.000 description 2
- 238000005498 polishing Methods 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- AKXKFZDCRYJKTF-UHFFFAOYSA-N 3-Hydroxypropionaldehyde Chemical compound OCCC=O AKXKFZDCRYJKTF-UHFFFAOYSA-N 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 239000003225 biodiesel Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000011143 downstream manufacturing Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 238000007517 polishing process Methods 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc 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
- C07C29/143—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 ketones
- C07C29/145—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 ketones with hydrogen or hydrogen-containing gases
-
- 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
- C07C29/60—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by elimination of -OH groups, e.g. by dehydration
-
- 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
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
- C07C29/88—Separation; Purification; Use of additives, e.g. for stabilisation by treatment giving rise to a chemical modification of at least one compound
- C07C29/90—Separation; Purification; Use of additives, e.g. for stabilisation by treatment giving rise to a chemical modification of at least one compound using hydrogen only
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (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 |
|---|---|---|---|
| GBGB0724232.4A GB0724232D0 (en) | 2007-12-12 | 2007-12-12 | Process |
| PCT/GB2008/051143 WO2009074821A1 (en) | 2007-12-12 | 2008-12-02 | Process for the production of 1,2-propanediol |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NZ586736A true NZ586736A (en) | 2012-05-25 |
Family
ID=39016468
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NZ586736A NZ586736A (en) | 2007-12-12 | 2008-12-02 | Process for the production of 1,2-propanediol |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US8334416B2 (enExample) |
| EP (1) | EP2222623B1 (enExample) |
| JP (1) | JP5576797B2 (enExample) |
| KR (1) | KR101611371B1 (enExample) |
| CN (1) | CN101896449B (enExample) |
| AR (1) | AR071266A1 (enExample) |
| AU (1) | AU2008334436B2 (enExample) |
| BR (1) | BRPI0820753B8 (enExample) |
| CA (1) | CA2708138C (enExample) |
| EA (1) | EA018513B1 (enExample) |
| ES (1) | ES2569602T3 (enExample) |
| GB (1) | GB0724232D0 (enExample) |
| MY (1) | MY150274A (enExample) |
| NZ (1) | NZ586736A (enExample) |
| PL (1) | PL2222623T3 (enExample) |
| TW (1) | TWI417272B (enExample) |
| WO (1) | WO2009074821A1 (enExample) |
| ZA (1) | ZA201004118B (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5350059B2 (ja) * | 2008-04-22 | 2013-11-27 | 三井化学株式会社 | プロピレングリコールの製造方法 |
| CN102070422B (zh) * | 2009-11-20 | 2013-06-19 | 中国科学院大连化学物理研究所 | 丙三醇脱水、加氢制备丙酮醇及1,2-丙二醇的方法 |
| KR101205897B1 (ko) | 2010-04-19 | 2012-11-29 | 한국과학기술연구원 | 복합금속산화물 담체에 담지된 귀금속 촉매 및 이를 이용한 1,2-프로판디올의 제조방법 |
| RU2548907C1 (ru) * | 2011-03-10 | 2015-04-20 | ДжиТиСи ТЕКНОЛОДЖИ ЮЭс ЭлЭлСи | Способ конверсии глицерина в пропиленгликоль |
| CN104098439A (zh) * | 2013-04-11 | 2014-10-15 | 中国科学院大连化学物理研究所 | 一种生物质乙二醇的精制方法 |
| CN116986970A (zh) * | 2023-07-27 | 2023-11-03 | 胜华新能源科技(东营)有限公司 | 一种酯交换副产1,2-丙二醇的纯化方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4334107A (en) * | 1980-11-11 | 1982-06-08 | Allied Chemical Corporation | Catalytic purification of phenol |
| JP2003073376A (ja) * | 2001-08-30 | 2003-03-12 | Daicel Chem Ind Ltd | 環状アセタールの製造方法 |
| US8017816B2 (en) * | 2002-04-22 | 2011-09-13 | The Curators Of The University Of Missouri | Method of producing lower alcohols from glycerol |
| GB0514593D0 (en) * | 2005-07-15 | 2005-08-24 | Davy Process Techn Ltd | Process |
| GB0614823D0 (en) | 2006-07-26 | 2006-09-06 | Davy Process Techn Ltd | Process |
| JP2008266234A (ja) * | 2007-04-23 | 2008-11-06 | Univ Of Tsukuba | グリセリンの還元方法 |
-
2007
- 2007-12-12 GB GBGB0724232.4A patent/GB0724232D0/en not_active Ceased
-
2008
- 2008-12-02 WO PCT/GB2008/051143 patent/WO2009074821A1/en not_active Ceased
- 2008-12-02 AU AU2008334436A patent/AU2008334436B2/en not_active Ceased
- 2008-12-02 CA CA2708138A patent/CA2708138C/en not_active Expired - Fee Related
- 2008-12-02 NZ NZ586736A patent/NZ586736A/en not_active IP Right Cessation
- 2008-12-02 BR BRPI0820753A patent/BRPI0820753B8/pt active IP Right Grant
- 2008-12-02 ES ES08859957.6T patent/ES2569602T3/es active Active
- 2008-12-02 KR KR1020107014804A patent/KR101611371B1/ko not_active Expired - Fee Related
- 2008-12-02 US US12/747,408 patent/US8334416B2/en active Active
- 2008-12-02 CN CN200880120369.9A patent/CN101896449B/zh active Active
- 2008-12-02 MY MYPI2010002727A patent/MY150274A/en unknown
- 2008-12-02 EP EP08859957.6A patent/EP2222623B1/en active Active
- 2008-12-02 JP JP2010537521A patent/JP5576797B2/ja not_active Expired - Fee Related
- 2008-12-02 EA EA201000970A patent/EA018513B1/ru not_active IP Right Cessation
- 2008-12-02 PL PL08859957T patent/PL2222623T3/pl unknown
- 2008-12-10 AR ARP080105349A patent/AR071266A1/es unknown
- 2008-12-11 TW TW097148271A patent/TWI417272B/zh not_active IP Right Cessation
-
2010
- 2010-06-09 ZA ZA2010/04118A patent/ZA201004118B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ZA201004118B (en) | 2011-08-31 |
| GB0724232D0 (en) | 2008-01-23 |
| JP2011506419A (ja) | 2011-03-03 |
| KR101611371B1 (ko) | 2016-04-12 |
| JP5576797B2 (ja) | 2014-08-20 |
| ES2569602T3 (es) | 2016-05-11 |
| AU2008334436B2 (en) | 2012-08-16 |
| US20110004030A1 (en) | 2011-01-06 |
| EA201000970A1 (ru) | 2011-02-28 |
| CA2708138C (en) | 2015-06-30 |
| EP2222623B1 (en) | 2016-02-17 |
| CN101896449B (zh) | 2016-08-03 |
| EP2222623A1 (en) | 2010-09-01 |
| PL2222623T3 (pl) | 2016-08-31 |
| BRPI0820753A2 (pt) | 2015-06-16 |
| TWI417272B (zh) | 2013-12-01 |
| WO2009074821A1 (en) | 2009-06-18 |
| KR20100103815A (ko) | 2010-09-28 |
| TW200938518A (en) | 2009-09-16 |
| US8334416B2 (en) | 2012-12-18 |
| AU2008334436A1 (en) | 2009-06-18 |
| CN101896449A (zh) | 2010-11-24 |
| CA2708138A1 (en) | 2009-06-18 |
| BRPI0820753B1 (pt) | 2017-10-17 |
| EA018513B1 (ru) | 2013-08-30 |
| AR071266A1 (es) | 2010-06-09 |
| MY150274A (en) | 2013-12-31 |
| BRPI0820753B8 (pt) | 2020-03-31 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PSEA | Patent sealed | ||
| RENW | Renewal (renewal fees accepted) | ||
| RENW | Renewal (renewal fees accepted) |
Free format text: PATENT RENEWED FOR 1 YEAR UNTIL 02 DEC 2016 BY CPA GLOBAL Effective date: 20151128 |
|
| LAPS | Patent lapsed |