CN101096335A - Method for preparing terephthalyl alcohol by hydrogenation of terephthalic acid - Google Patents
Method for preparing terephthalyl alcohol by hydrogenation of terephthalic acid Download PDFInfo
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- CN101096335A CN101096335A CNA2006100284795A CN200610028479A CN101096335A CN 101096335 A CN101096335 A CN 101096335A CN A2006100284795 A CNA2006100284795 A CN A2006100284795A CN 200610028479 A CN200610028479 A CN 200610028479A CN 101096335 A CN101096335 A CN 101096335A
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- terephthalic acid
- terephthalyl alcohol
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- hydrogenation
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Abstract
The invention discloses a terephthalyl alcohol preparing method by hydrotreating terephthalic acid, which proceeds with the hydrogenation reaction in the accelerant and hydrogen gas condition. The reaction is made in the solvent water, wherein the proportion by weight of terephthalic acid and water is 1: (5-20), the reaction temperature is 180-300Deg. C, the hydrogen pressure is 5.0-10.0MPa, the reaction time is 3-8 hours, the accelerant regards AL2O3 as the carrier, and the load active component is Ru, Sn and B, the mole ratio of Ru and Sn is 1:(0.5-2.0), the total content of the active component Ru and Sn in the accelerant is 5-12wt%, the content of B is 5-20wt%, the grain size of the accelerant is 80-250 mesh size, the usage of the accelerant in the reaction system is 1-5wt%. The invention is provided with the low material cost, which is fit for the mass industry production.
Description
Technical field
The present invention relates to a kind of is the method for catalytic material hydrogenation preparing terephthalyl alcohol by terephthalic acid, the catalyzer that this method adopts be a kind of be the loaded catalyst of active ingredient with metal Ru, Sn and B.
Background technology
Terephthalyl alcohol is a kind of important organic polymer intermediate, owing on its structure two active hydroxyls are arranged, can generate multiple polymers with having the compound reaction that hydroxyl, aldehyde radical, carboxyl etc. have a α reactive hydrogen, they are main raw materials of producing products such as softening agent, synthon, synthetic resins and tackiness agent.The production of terephthalyl alcohol is raw material with the p-Xylol mainly at present, and hydrolysis makes again after chlorination.As U.S. Pat 3,546,301 disclosed technology are to be solvent with the tetrahydrofuran (THF), and anhydrous sodium carbonate is a catalyzer, and to the xylylene dichlorides hydrolysis, the yield of terephthalyl alcohol is 73%.US3,993,699 disclosed technology be with to xylylene dichlorides in the presence of the triethylamine catalyzer, with the sodium acetate esterification, again through the NaOH hydrolysis, yield surpasses 95%.The shortcoming of these methods is that reaction scheme is long, side reaction is many, and chlorination reaction causes corrosion and produces equipment to be polluted.It is most economical directly preparing terephthalyl alcohol by terephthalic acid by the carboxyl hydrogenation in theory, but the carboxyl hydrogenation reaction of terephthalic acid is carried out difficulty generally speaking, and speed of reaction and product yield are all lower.The catalyzer that employing contains precious metals such as Pt or Re can suitably improve the speed and the yield of reaction, but causes it to lack practical value because of catalyzer is very expensive.Comparatively speaking, terephthalic acid and lower aliphatic alcohols esterification generate that to carry out ester through hydrogenation behind the corresponding ester more much easier.As the disclosed technology of Japanese Patent JP7431435 is to be raw material with the dimethyl terephthalate (DMT), carries out hydrogenation reaction in solvent methanol He in the presence of the Cu-Cr catalyzer, and the terephthalyl alcohol yield reaches about 65%.Because yield is on the low side, this production method also lacks industrialized value.In addition, be starting raw material with the terephthalic acid, also can adopt the operational path of first esterification posthydrolysis to prepare terephthalyl alcohol.Being to use anionite-exchange resin as catalyzer as the disclosed technology of Japanese Patent JP63014745, is that raw material prepares terephthalyl alcohol through hydrolysis with the diethyl terephthalate.And there is the shortcoming that reaction scheme is long, side reaction is many, production cost is high equally in this method.
Summary of the invention
The invention provides a kind of method by terephthalic acid hydrogenation system terephthalyl alcohol, it adopts a kind of hydrogenation catalyst efficiently, by the direct hydrogenation preparing terephthalyl alcohol of terephthalic acid, solved under the general condition carboxyl hydrogenation reaction of terephthalic acid and carried out this technical problem of difficulty.
Below be the detailed technical scheme of the present invention:
A kind of method by terephthalic acid hydrogenation system terephthalyl alcohol, this method comprise that terephthalic acid carries out hydrogenation reaction in the presence of catalyzer in hydrogen atmosphere.Be reflected in the aqueous solvent and carry out, the weight ratio of terephthalic acid and water is 1: (5～20), temperature of reaction are 180～300 ℃, and hydrogen pressure is 5.0～10.0MPa, and the reaction times is 3～8 hours.Catalyzer is with Al
2O
3Be carrier, load active component metal Ru, metal Sn and B.The mol ratio of Ru and Sn is 1: (0.5～2.0), the total content of activity component metal Ru and metal Sn is 5～12wt% in the catalyzer, the content of B is 5～20wt%, and catalyst grain size is 80～250 orders, and catalyst levels is counted 1～5wt% with the total amount of reaction system.
In technique scheme, the mol ratio of activity component metal Ru and metal Sn is preferably 1 in the described catalyzer: (0.5～1.5); The total content of active ingredient Ru and Sn is preferably 6～10wt% in the catalyzer, and the content of B is preferably 7～18wt%.
The weight ratio of described terephthalic acid and water is preferably 1: (8～15); Temperature of reaction is preferably 200～250 ℃; Hydrogen pressure is preferably 8～10MPa; Catalyst consumption is preferably 1～3wt% in the total amount of reaction system.
The catalyzer that reaction is adopted can prepare in order to the method that following contriver is recommended:
The starting material of Ru, Sn and B is generally selected corresponding water-soluble salt for use, as RuCl
33H
2O, SnCl
22H
2O and NaBH
4Dispose Ru salt and Sn salt brine solution respectively, after the dissolving both are mixed fully.With carrier A l
2O
3Join in the above-mentioned mixing solutions and stir, and left standstill aging 8～25 hours.Quantitative boron salt is made into the aqueous solution, add in the above-mentioned dip compound after, after filtration, washing, drying, logical at a certain temperature hydrogen reducing can obtain required catalyzer.Reduction temperature generally is controlled at 200～650 ℃, is preferably 200～400 ℃.Recovery time is 0.5～5 hour, is preferably 1～3 hour.Hydrogen flowing quantity is generally 80～250ml/min, is preferably 100～200ml/min.
Key of the present invention is to have adopted a kind of ideal hydrogenation catalyst, and this catalyzer does not use expensive precious metals such as Pt or Re, has very ideal reactive behavior and very high selectivity in the carboxyl hydrogenation reaction that is used for terephthalic acid.Compared with prior art, terephthalyl alcohol preparation method provided by the invention is more economical, and raw materials cost is lower, helps large-scale industrial production.
Below by specific embodiment the present invention is further described, yield is defined as in an embodiment:
Below will the invention will be further described by specific embodiment.
Embodiment
One, Preparation of catalysts:
[embodiment 1]
With 2.59gRuCl
33H
2O is dissolved in the 14ml deionized water, adds 1.34g SnCl then
22H
2The O dissolving adds 20g carrier A l again
2O
3Stir, obtain blackish green mashed prod, left standstill aging 15 hours.Get 11.65g NaBH
4Be dissolved in the 10ml deionized water, this solution dropwise added in the above-mentioned mashed prod, leave standstill 30min after, filter and give a baby a bath on the third day after its birth time, under 70～90 ℃ of temperature dry 6 hours with deionized water.Getting granularity after the grinding is that 80～250 purpose particles are catalyst precursor, and hydrogen reducing 2 hours are used in heating, and hydrogen flowing quantity is 150ml/min, promptly obtains the used catalyzer finished product of hydrogenation reaction.
[embodiment 2～8]
Change the consumption of carrier and initiator in each catalyzer, all the other are with embodiment 1.
The composition and the content of the catalyst activity component that each embodiment makes see Table 1.
Table 1
| Ru:: Sn (mol ratio) | Ru+Sn content (wt%) | B content (wt%) | |
| Embodiment 1 | 1∶0.6 | 6.8 | 13.3 |
| Embodiment 2 | 1∶0.8 | 7.7 | 13.2 |
| Embodiment 3 | 1∶0.5 | 6.0 | 7.1 |
| Embodiment 4 | 1∶0.7 | 7.2 | 13.2 |
| Embodiment 5 | 1∶0.8 | 7.4 | 16.8 |
| Embodiment 6 | 1∶0.9 | 8.1 | 13.8 |
| Embodiment 7 | 1∶1.0 | 8.5 | 14.5 |
| Embodiment 8 | 1∶1.5 | 10.0 | 17.8 |
Two, hydrogenation reaction:
[embodiment 9]
Adopt the resulting catalyzer of the foregoing description to carry out the reaction of terephthalic acid hydrogenation preparing terephthalyl alcohol:
15g terephthalic acid and 150ml water (solvent) are added in the 300ml autoclave simultaneously, add the catalyzer of aequum in proportion.Closed reactor is extracted air in the still out, feeds hydrogen exchange, under the 2.0MPa hydrogen pressure, is heated with stirring to temperature of reaction, feeds hydrogen again to reaction pressure, begins to react timing, keeps required hydrogen pressure to reaction to finish.Cooling back filtration catalizer, the product terephthalyl alcohol with in the gas chromatographic analysis reaction solution calculates its concentration by marker method.
[embodiment 10～16]
Change terephthalic acid charging capacity, catalyst levels and other hydrogenation conditions, all the other are with embodiment 9.
The catalyzer that each embodiment adopts, concrete reaction conditions see Table 2, and wherein the yield of reaction times, solvent types and target product terephthalyl alcohol sees Table 3.
Table 2.
| Catalyzer (embodiment) | Catalyst levels (wt%) | Raw material: water (weight ratio) | Reaction hydrogen pressure (MPa) | Temperature of reaction (℃) | |
| Embodiment 9 | 1 | 3.0 | 1∶10 | 10 | 230 |
| Embodiment 10 | 2 | 2.0 | 1∶12 | 10 | 200 |
| Embodiment 11 | 3 | 1.3 | 1∶8 | 10 | 200 |
| Embodiment 12 | 4 | 1.6 | 1∶12 | 10 | 230 |
| Embodiment 13 | 5 | 3.0 | 1∶11 | 10 | 230 |
| Embodiment 14 | 6 | 1.0 | 1∶15 | 10 | 230 |
| Embodiment 15 | 7 | 1.3 | 1∶8 | 8 | 250 |
| Embodiment 16 | 8 | 1.2 | 1∶15 | 8 | 250 |
In the table, catalyst levels: catalyzer is at the content of reaction system; Raw material: terephthalic acid.
Table 3
| Reaction times (hr) | Terephthalyl alcohol yield (%) | |
| Embodiment 9 | 5.5 | 81.0 |
| Embodiment 10 | 3.2 | 85.5 |
| Embodiment 11 | 5.5 | 83.6 |
| Embodiment 12 | 5 | 91.6 |
| Embodiment 13 | 5 | 93.2 |
| Embodiment 14 | 5 | 90.8 |
| Embodiment 15 | 6 | 86.5 |
| Embodiment 16 | 4 | 90.7 |
Claims (8)
1, a kind of method by terephthalic acid hydrogenation system terephthalyl alcohol, this method comprises that terephthalic acid carries out hydrogenation reaction in the presence of catalyzer in hydrogen atmosphere, be reflected in the aqueous solvent and carry out, the weight ratio of terephthalic acid and water is 1: (5～20), temperature of reaction is 180～300 ℃, hydrogen pressure is 5.0～10.0MPa, and the reaction times is 3～8 hours, and catalyzer is with Al
2O
3Be carrier, load active component metal Ru, metal Sn and B, the mol ratio of Ru and Sn is 1: (0.5～2.0), the total content of activity component metal Ru and metal Sn is 5～12wt% in the catalyzer, the content of B is 5～20wt%, catalyst grain size is 80～250 orders, and catalyst levels is counted 1～5wt% with the total amount of reaction system.
2, the method for system terephthalyl alcohol according to claim 1 is characterized in that the mol ratio of activity component metal Ru and metal Sn is 1 in the described catalyzer: (0.5～1.5).
3, the method for system terephthalyl alcohol according to claim 1 is characterized in that the total content of active ingredient Ru and Sn is 6～10wt% in the described catalyzer.
4, the method for system terephthalyl alcohol according to claim 1, the content that it is characterized in that active ingredient B in the described catalyzer is 7～18wt%
5, the method for system terephthalyl alcohol according to claim 1, the weight ratio that it is characterized in that described terephthalic acid and water is 1: (8～15).
6, the method for system terephthalyl alcohol according to claim 1 is characterized in that described temperature of reaction is 200～250 ℃.
7, the method for system terephthalyl alcohol according to claim 1 is characterized in that described hydrogen pressure is 8～10MPa.
8, the method for system terephthalyl alcohol according to claim 1 is characterized in that described catalyst consumption counts 1～3wt% with the total amount of reaction system.
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| CN200610028479A CN100584813C (en) | 2006-06-30 | 2006-06-30 | Method for preparing terephthalyl alcohol by hydrogenation of terephthalic acid |
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|---|---|---|---|
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| CN100584813C CN100584813C (en) | 2010-01-27 |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103880594A (en) * | 2012-12-19 | 2014-06-25 | 中国石油化工股份有限公司 | Method for preparing 1,4-benzenedimethanol by performing atmospheric oxidation on p-xylene |
| CN105646152A (en) * | 2014-12-04 | 2016-06-08 | 中国石油化工股份有限公司 | Preparation method of 1, 2-benzenedimethanol |
-
2006
- 2006-06-30 CN CN200610028479A patent/CN100584813C/en active Active
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103880594A (en) * | 2012-12-19 | 2014-06-25 | 中国石油化工股份有限公司 | Method for preparing 1,4-benzenedimethanol by performing atmospheric oxidation on p-xylene |
| CN103880594B (en) * | 2012-12-19 | 2015-10-21 | 中国石油化工股份有限公司 | The method of p-Xylol atmospheric oxidation terephthalyl alcohol |
| CN105646152A (en) * | 2014-12-04 | 2016-06-08 | 中国石油化工股份有限公司 | Preparation method of 1, 2-benzenedimethanol |
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| CN100584813C (en) | 2010-01-27 |
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