WO1992011224A1 - Process for the preparation of glycol ethers - Google Patents
Process for the preparation of glycol ethers Download PDFInfo
- Publication number
- WO1992011224A1 WO1992011224A1 PCT/GB1991/002276 GB9102276W WO9211224A1 WO 1992011224 A1 WO1992011224 A1 WO 1992011224A1 GB 9102276 W GB9102276 W GB 9102276W WO 9211224 A1 WO9211224 A1 WO 9211224A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- alcohol
- process according
- double hydroxide
- catalyst
- anions
- Prior art date
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/02—Preparation of ethers from oxiranes
- C07C41/03—Preparation of ethers from oxiranes by reaction of oxirane rings with hydroxy groups
Definitions
- This invention relates to a process for the preparation of glycol ethers.
- Glycol ethers are useful as jet anti-icing fluids, brake fluid blending components and solvents for paints, inks and the like. They may be produced by reacting an alcohol with an olefin oxide in the presence of either a basic or acidic catalyst.
- Anionic double hydroxide clays are well-known materials. They are described in, for example, "Anionic Clay Minerals", W.T.
- Mg(OH>2 * In brucite magnesium is octahedrally surrounded by six oxygens in the form of hydroxide; the octahedral units then, through edge sharing, form infinite sheets. The sheets are stacked on top of each other by hydrogen bonds. If some of the magnesium in the lattice is isomorphously replaced by a higher charged cation, e.g.
- Anionic double hydroxide clays have, in the dehydrated form, the empirical formula: [M a 2+ N b 3 + (OH) (2a+2b )][X]b in which M 2+ is a divalent metal cation; N + is a trivalent metal cation; X is one equivalent of an anion; and a and b represents the relative proportions of M and N in the structure.
- M 2+ is Mg 2+ personally Fe 2+ , Co 2+ , Ni 2+ and/or Zn 2+
- N 3+ is Al 3+ , Cr 3+ and/or Fe + .
- the divalent metal may be wholly or partly replaced by lithium, the all-lithium form having the empirical formula:
- M 2+ is Mg 2+
- N + is Al +
- X is carbonate
- a/b is in the range of 1:1 to 5:1.
- Such minerals occur in a hydrated form.
- calcined anionic double hydroxide clays have catalytic activity.
- US Patent No. 4458026 discloses that catalysts prepared by calcination of anionic double hydroxide clays may be used to perform aldol condensations.
- Japanese Patent Application No. 54-111047 discloses that calcined anionic double hydroxide clays may be used to prepare alkylene glycol ether acetates.
- EP-A-339426 discloses the use of calcined hydrotalcite for the ethoxylation or propoxylation of compounds containing active hydrogen atoms.
- Anionic double hydroxide clays in their naturally-occurring or as-synthesised form have a layered structure. Calcination of the material leads to collapse of this layered structure (see for example Sato et al, Reactivity of Solids 1986.2 253-260, and Sato et al, Ind. Eng. Chem. Prod. Res. Dev. 1986, _25_, 89-92), and results in a poorly-crystalline magnesium oxide-type structure. All the above documents require that the anionic double hydroxide clay be used as a catalyst in the calcined form, that is, in a form having a collapsed layer structure.
- the present invention provides a process for the preparation of a glycol ether by reacting an olefin oxide with an alcohol over a catalyst; characterised in that the catalyst is an anionic double hydroxide clay with a substantially intact layered structure, the inter-lameliar anions consisting substantially of the anions of the reactant alcohol.
- An anionic double hydroxide clay with a substantially intact layered structure can be obtained in two different ways. It can of course be obtained by using the material in its naturally-occurring or as-synthesised form, without heating to a temperature sufficient to collapse the layered structure. In general, heating to a temperature of greater than 300 ⁇ C should be avoided. Secondly, the anionic double hydroxide clay may be calcined to a temperature which causes collapse of the layered structure, and the resulting material subsequently rehydrated. This rehydration causes layers to reform substantially intact.
- Naturally-occurring anionic double hydroxide clays have an intact layered structure; the inter-lamellar anions are mainly carbonate. Such materials have low activity as catalysts for the preparation of glycol ethers; calcination enhances their activity.
- the inter-lamellar carbonate ions are exchanged with the anion of an alcohol, the resulting material has significantly improved activity for the preparation of glycol ethers.
- Such ion exchange can be carried out prior to use as a catalyst by using ion exchange techniques. It can also, however, be accomplished by passing an alcohol over the anionic double hydroxide clay.
- One possible embodiment of the latter method is to conduct a process according to the invention except that the catalyst is an anionic double hydroxide clay with a substantially intact layered structure, the inter-lameliar anions being other than the anions of the reactant alcohol. Conversion of the feedstock is initially low; however, after a period of time, the conversion increases as the inter-lamellar anions exchange with the reactant alcohol resulting in an effective catalyst. When operating in such a manner, the reaction is preferably carried out by passing a continuous flow of fresh alcohol feed over the catalyst.
- the anionic double hydroxide clay has a framework structure including magnesium, divalent iron, cobalt, zinc and/or lithium together with aluminium, chromium and/or trivalent iron.
- the framework structure comprises magnesium and aluminium.
- Anionic double hydroxide clays can be prepared by known methods, for example by the method described in US 4458026. In general, solutions of soluble salts of the relevant metals are mixed together with an alkali metal hydroxide and an alkali metal carbonate. The resulting mixture is vigorously stirred until a slurry is formed. The slurry is then heated, typically to a temperature between 50 and 100 ⁇ C, preferably 60 to 75 ⁇ C, until sufficient crystallisation occurs. The resulting product is an anionic double hydroxide clay in which the interlamellar anions are carbonate. Materials containing other ions, for example bicarbonate or carboxylic anions, may be prepared either by exchange of the carbonate anions or by adapting the synthesis method so that the other anions are incorporated.
- the anionic double hydroxide clay prepared for example as described above may be subjected to calcination.
- this involves heating to a temperature of at least 300*C, preferably 300 to 550*C, especially 350 to 500 ⁇ C, under non-reducing conditions.
- the heating may be carried out under vacuum, in an inert gas or, preferably, in an oxidising atmosphere, preferably air. Heating is carried out for a period of time typically between 10 and 30 hours.
- Such treatment causes the collapse of the double hydroxide layered structure and the decomposition of decomposable anions, and, generally, results in an oxide material having a structure related to that of MgO. Subsequent rehydration causes the layered structure to reform.
- the alcohol used in the process according to the invention may be an aliphatic, cycloaliphatic or aromatic alcohol, preferably having up to 8 carbon atoms.
- An aliphatic alcohol preferably has up to 6, more preferably up to 4, carbon atoms.
- Typical aliphatic alcohols include methanol and ethanol.
- An example of a suitable cycloaliphatic alcohol is cyclohexanol, and an example of a suitable aromatic alcohol is phenol.
- More than one alcohol group may be present if desired, but preferably the alcohol is a mono alcohol. Mixtures of alcohols may be used if desired. The alcohol is suitably used in excess if it is desired to produce a mono glycol ether and suppress the formation of oligomeric products.
- the molar ratio of alcohol to olefin oxide is at least 2:1, especially at least 5:1, most preferably at least 10:1.
- the olefin oxide preferably has up to 10, especially up to 8, carbon atoms, and may for example by derived from an alkene, for example ethene or propene, or from a arylalkene such as styrene.
- ethanol is reacted with propylene oxide to produce a mixture of the primary and secondary glycol ethers, 2-ethoxypropan-l-ol and l-ethoxypropan-2-ol. It is a major advantage of the process according to the present invention that the reaction proceeds with a very high selectivity to the secondary alcohol product, which is in general the desired product.
- the reaction may be carried out in the vapour phase or, especially, the liquid phase.
- the optimum reaction temperature will of course depend upon the particular reactants used, but will in general be within the range of from 0 to 250"C, especially 70 to 200°C.
- the reaction may be carried out at atmospheric or elevated pressure, for example up to 100 barg.
- Example 1 illustrates the invention.
- the supernatant was then decanted and the slurry was concentrated by centrifuging (2000 rpm, 1120G, 1 hour) and then decanting.
- the concentrated slurry was then loaded into dialysis tubing (Medicell Visking size 6-27/32").
- the sealed tubes were then continuously washed in distilled water until the effluent water was chloride free (tested by 0.1 mol dm -3 AgN ⁇ 3 solution) and the conductivity was below 20 ⁇ S cm- .
- the dialysis tubes were then opened and the recovered slurry was slowly dried in a fan oven at 60 ⁇ C. Part of the oven dried material was broken down and sieved with the 0.5-1.0 mm size range being collected.
- the X-ray diffraction pattern (XRD) showed the material to be hydrotalcite with a d(003) spacing of 7.69 Angstroms.
- Example 2 Calcination Part of the dried cake from Example 1 Section A was calcined at 400*C for 18 hours in air. It was then broken down and sieved with the 0.5-1.0 mm size range being collected. The XRD indicated a poorly crystalline magnesium oxide-like phase.
- a commercially available calcined Hydrotalcite (KW2015) was obtained from Kyowa Chemical Industry Co. Ltd.
- the sample of KW2015 was supplied as pellets of 1.0-2.0 mm diameter.
- Example 2
- Example 1 Rehydrated Calcined Hydrotalcite (Commercial Sample) The procedure described in Example 2 was repeated except that after the aqueous rehydration step, the water was decanted and the pellets were dried under flowing nitrogen at lOO'C.
- Comparison Material 2 Magnesium Hydroxide The preparation described in Example 1 Section A was repeated except that the chloride solution contained only [Mg(H 2 0)5]Cl2 (543 g, 2.67 moles). The resulting material was shown by XRD to have the Brucite structure. Comparison Material 3 Magnesium Hydroxide
- a commercially available sample of powdered magnesium hydroxide (AnalaR grade from BDH) having the Brucite structure was made into pellets by pressing to 12 tonnes in a 35 mm diameter die. These pellets were broken down and sieved with the 0.5-1.9 mm size range being collected.
- a Varian 3700 fitted with a Porapak Q column (1.0 m, 6 mm outside diameter, 2 mm inside diameter, 80-100 mesh) operating with a temperature programme (llO'C for 7 minutes, ramping 60 ⁇ C/minute to 220 ⁇ C) was used to determine the propylene oxide conversion.
- a Pye-Unicam 4500 fitted with a WCOT fused silica capillary column (50 m, 0.25 mm internal diameter, CP-Sil-5) operating with a temperature programme (80 ⁇ C for 10 minutes, ramping 6°C/minute to 200 ⁇ C) was used to determine the relative amounts of l-ethoxypropan-2-ol (1EP2) and 2-ethyoxypropan-l-ol (2EP1).
- Example 5 This Example reports the testing of the material from Example 1 Section C. Comparison Test 1 This comparison reports the testing of the material from Example 1 Section B.
- Example 5 This Example reports the testing of the material from Example 1 Section C.
- Example 6 This Example reports the testing of the material from Example 2.
- Example 7 This Example reports the testing of the material from Example 2.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9027632.0 | 1990-12-20 | ||
GB9027632A GB9027632D0 (en) | 1990-12-20 | 1990-12-20 | Process for the preparation of glycol ethers |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1992011224A1 true WO1992011224A1 (en) | 1992-07-09 |
Family
ID=10687319
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/GB1991/002276 WO1992011224A1 (en) | 1990-12-20 | 1991-12-19 | Process for the preparation of glycol ethers |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP0515636A1 (en) |
JP (1) | JPH05503946A (en) |
AU (1) | AU9096691A (en) |
CA (1) | CA2076376A1 (en) |
GB (1) | GB9027632D0 (en) |
WO (1) | WO1992011224A1 (en) |
ZA (1) | ZA9110086B (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995002570A1 (en) * | 1993-07-14 | 1995-01-26 | HÜLS Aktiengesellschaft | Method of preparing alkoxylates |
WO1995004024A1 (en) * | 1993-07-28 | 1995-02-09 | Basf Aktiengesellschaft | Method for preparing alkoxylation products in the presence of additive-modified mixed hydroxides |
WO1995017248A1 (en) * | 1993-12-22 | 1995-06-29 | Kao Corporation | Alkoxylation catalyst, process for the preparation of the catalyst and process for preparing alkoxylate with the use of the catalyst |
WO1997000842A1 (en) * | 1995-06-22 | 1997-01-09 | Bp Chemicals Limited | Synthesis of glycol ethers |
EP0952138A1 (en) * | 1998-04-25 | 1999-10-27 | BP Chemicals Limited | Synthesis of glycol ethers |
US6124506A (en) * | 1995-06-22 | 2000-09-26 | Bp Chemicals Limited | Synthesis of glycol ethers |
CN1063099C (en) * | 1996-10-22 | 2001-03-14 | 中国石油化工总公司上海石油化工研究院 | Catalyzer for preparing propylene-glycol ether |
CN1087651C (en) * | 1997-06-06 | 2002-07-17 | 中国石油化工总公司 | Solid alkali catalyst for synthesis of propanediol ether |
CN1089276C (en) * | 1999-04-01 | 2002-08-21 | 北京化工大学 | Carried hydrotalcite catlyst and the preparation of aliphatic alcohol ether acetate |
US6548714B1 (en) | 1998-09-05 | 2003-04-15 | Basf Aktiengesellschaft | Method for producing polyetherols by ring-opening polymerisation of alkylene oxides |
DE102008002091A1 (en) | 2007-05-31 | 2008-12-11 | Basf Se | Monoalkylene glycol monoether production involves reacting alcohol with alkylene oxide in presence of heterogeneous catalyst in liquid phase |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005145862A (en) * | 2003-11-13 | 2005-06-09 | Nippon Shokubai Co Ltd | Method for producing aromatic ethers |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2035306A (en) * | 1978-10-05 | 1980-06-18 | Showa Denko Kk | Process for preparing a monoalkylene glycol monoether |
EP0073141A2 (en) * | 1981-08-21 | 1983-03-02 | The British Petroleum Company p.l.c. | Method for promoting the activity and/or extending the life of cation-exchangeable layered clay catalysts in proton-catalysed reactions |
EP0083970A1 (en) * | 1982-01-09 | 1983-07-20 | The British Petroleum Company p.l.c. | Use of stabilised pillared interlayered clays as catalysts in reactions capable of catalysis by protons |
EP0250168A1 (en) * | 1986-06-19 | 1987-12-23 | The British Petroleum Company p.l.c. | Production of glycol ethers |
-
1990
- 1990-12-20 GB GB9027632A patent/GB9027632D0/en active Pending
-
1991
- 1991-12-19 CA CA 2076376 patent/CA2076376A1/en not_active Abandoned
- 1991-12-19 WO PCT/GB1991/002276 patent/WO1992011224A1/en not_active Application Discontinuation
- 1991-12-19 JP JP50146392A patent/JPH05503946A/en active Pending
- 1991-12-19 AU AU90966/91A patent/AU9096691A/en not_active Abandoned
- 1991-12-19 EP EP19920901355 patent/EP0515636A1/en not_active Ceased
- 1991-12-20 ZA ZA9110086A patent/ZA9110086B/en unknown
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2035306A (en) * | 1978-10-05 | 1980-06-18 | Showa Denko Kk | Process for preparing a monoalkylene glycol monoether |
EP0073141A2 (en) * | 1981-08-21 | 1983-03-02 | The British Petroleum Company p.l.c. | Method for promoting the activity and/or extending the life of cation-exchangeable layered clay catalysts in proton-catalysed reactions |
EP0083970A1 (en) * | 1982-01-09 | 1983-07-20 | The British Petroleum Company p.l.c. | Use of stabilised pillared interlayered clays as catalysts in reactions capable of catalysis by protons |
EP0250168A1 (en) * | 1986-06-19 | 1987-12-23 | The British Petroleum Company p.l.c. | Production of glycol ethers |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995002570A1 (en) * | 1993-07-14 | 1995-01-26 | HÜLS Aktiengesellschaft | Method of preparing alkoxylates |
WO1995004024A1 (en) * | 1993-07-28 | 1995-02-09 | Basf Aktiengesellschaft | Method for preparing alkoxylation products in the presence of additive-modified mixed hydroxides |
WO1995017248A1 (en) * | 1993-12-22 | 1995-06-29 | Kao Corporation | Alkoxylation catalyst, process for the preparation of the catalyst and process for preparing alkoxylate with the use of the catalyst |
US6124506A (en) * | 1995-06-22 | 2000-09-26 | Bp Chemicals Limited | Synthesis of glycol ethers |
WO1997000842A1 (en) * | 1995-06-22 | 1997-01-09 | Bp Chemicals Limited | Synthesis of glycol ethers |
CN1063099C (en) * | 1996-10-22 | 2001-03-14 | 中国石油化工总公司上海石油化工研究院 | Catalyzer for preparing propylene-glycol ether |
CN1087651C (en) * | 1997-06-06 | 2002-07-17 | 中国石油化工总公司 | Solid alkali catalyst for synthesis of propanediol ether |
EP0952138A1 (en) * | 1998-04-25 | 1999-10-27 | BP Chemicals Limited | Synthesis of glycol ethers |
US6291720B1 (en) | 1998-04-25 | 2001-09-18 | Bp Chemicals Limited | Synthesis of glycol ethers |
SG85640A1 (en) * | 1998-04-25 | 2002-01-15 | Bp Chem Int Ltd | Synthesis of glycol ethers |
US6548714B1 (en) | 1998-09-05 | 2003-04-15 | Basf Aktiengesellschaft | Method for producing polyetherols by ring-opening polymerisation of alkylene oxides |
CN1089276C (en) * | 1999-04-01 | 2002-08-21 | 北京化工大学 | Carried hydrotalcite catlyst and the preparation of aliphatic alcohol ether acetate |
DE102008002091A1 (en) | 2007-05-31 | 2008-12-11 | Basf Se | Monoalkylene glycol monoether production involves reacting alcohol with alkylene oxide in presence of heterogeneous catalyst in liquid phase |
Also Published As
Publication number | Publication date |
---|---|
EP0515636A1 (en) | 1992-12-02 |
GB9027632D0 (en) | 1991-02-13 |
ZA9110086B (en) | 1993-06-21 |
JPH05503946A (en) | 1993-06-24 |
AU9096691A (en) | 1992-07-22 |
CA2076376A1 (en) | 1992-06-21 |
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