CN202638397U - 1,4-cyclohexanedicarboxylates continuous fixed bed reactor - Google Patents
1,4-cyclohexanedicarboxylates continuous fixed bed reactor Download PDFInfo
- Publication number
- CN202638397U CN202638397U CN 201220236208 CN201220236208U CN202638397U CN 202638397 U CN202638397 U CN 202638397U CN 201220236208 CN201220236208 CN 201220236208 CN 201220236208 U CN201220236208 U CN 201220236208U CN 202638397 U CN202638397 U CN 202638397U
- Authority
- CN
- China
- Prior art keywords
- reactor
- fixed bed
- cyclohexanedicarboxylates
- order reactor
- bed reactors
- 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.)
- Expired - Lifetime
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- PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical class OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 title abstract 2
- 239000000463 material Substances 0.000 claims abstract description 14
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 claims description 8
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 abstract description 13
- 239000003054 catalyst Substances 0.000 abstract description 7
- 238000005984 hydrogenation reaction Methods 0.000 abstract description 5
- 238000006243 chemical reaction Methods 0.000 abstract description 4
- 230000002035 prolonged effect Effects 0.000 abstract description 2
- 229920000728 polyester Polymers 0.000 description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229920006305 unsaturated polyester Polymers 0.000 description 2
- 229920005830 Polyurethane Foam Polymers 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000011496 polyurethane foam Substances 0.000 description 1
- RCJOMOPNGOSMJU-UHFFFAOYSA-N prismane Chemical compound C12C3C4C1C4C32 RCJOMOPNGOSMJU-UHFFFAOYSA-N 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 238000004017 vitrification Methods 0.000 description 1
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- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
The utility model relates to a 1,4-cyclohexanedicarboxylates continuous fixed bed reactor which has the innovative characteristics that a first-order reactor and a second-order reactor, connected in series, are included; a material inlet is formed in the top end of the first-order reactor; a material outlet is formed in the bottom end of the second-order reactor; and the first-order reactor and the second-order reactor are tube type fixed bed reactors. Material, namely dimethyl terephthalate, is subjected to ring hydrogenation continuously through tube-type fixed bed reactors connected in series, the material conversion rate reaches more than 98%, and is improved by 1 to 2% as compared with the traditional independent fixed bed reactor, and in addition, the service life of a catalyst is prolonged to be more than one year.
Description
Technical field
The utility model relates to a kind of fixed bed reactors, particularly a kind of Isosorbide-5-Nitrae-cyclohexane diacid dimethyl ester serialization fixed bed reactors.
Background technology
1,4-CHDM is saturated polyester and the synthetic intermediate of unsaturated polyester (UP) of coating, printing ink, adhesive, insulating materials and some specific use aspects.Have very high vitrification point by its goods that produce, have good hardness and certain pliability is arranged, the gained light-colored resin has good heat endurance and preferably dissolubility and against weather is arranged.For the manufacture of polyester fiber, polyester electrical appliance, unsaturated polyester resin, polyester glaze, polyurethane foam plastics, and for the production of lubricant and hydraulic fluid.
In the process of the synthetic 1,4-CHDM of dimethyl terephthalate (DMT) two-step catalysis hydrogenation, at first need dimethyl terephthalate (DMT) ring Hydrogenation is got Isosorbide-5-Nitrae-cyclohexane diacid dimethyl ester.Traditional Isosorbide-5-Nitrae-cyclohexane diacid dimethyl ester reactor adopts independently fixed bed reactors, and it utilizes catalyst to encircle hydrogenation reaction and makes.The shortcoming of this kind fixed bed reactors is: conversion ratio is lower, and the life-span of benefiting from of catalyst only has 4 to 6 months.
Summary of the invention
But the technical problems to be solved in the utility model provides the high and extending catalyst of a kind of conversion ratio one prismane dimethyl ester serialization fixed bed reactors in service life.
For solving the problems of the technologies described above, the technical solution of the utility model is: a kind of 1,4-cyclohexane diacid dimethyl ester serialization fixed bed reactors, its innovative point is: comprise A reactor and second reactor that series connection arranges, the top of described A reactor arranges material inlet, and the bottom of second reactor arranges material outlet; Described one-level, second reactor are calandria type fixed bed reactor.
The utility model has the advantage of: the material dimethyl terephthalate (DMT) encircles hydrogenation by the calandria type fixed bed reactor of profit series connection continuously, materials conversion rate reaches more than 98%, intersect traditional independent fixed bed reactors and improve 1-2%, in addition, prolonged the service life of catalyst, reached more than 1 year.
Description of drawings
Fig. 1 is Isosorbide-5-Nitrae in the utility model-cyclohexane diacid dimethyl ester serialization fixed bed reactors structural representation.
The specific embodiment
As shown in Figure 1, comprise A reactor 1, second reactor 2, material inlet 3 and material outlet 4.
Above-mentioned A reactor 1 and second reactor 2 series connection arrange, and A reactor 1 bottom discharging opening is communicated with second reactor 2 top charging apertures, on the top of A reactor 1 material inlet 3 is set, and the bottom of second reactor 2 arranges material outlet 4.
A reactor 1 and second reactor 2 all adopt calandria type fixed bed reactor, and catalyst adopts alundum (Al2O3) as the metal palladium catalyst of carrier.
Claims (1)
1. Isosorbide-5-Nitrae-cyclohexane diacid dimethyl ester serialization fixed bed reactors is characterized in that: comprise A reactor and second reactor that series connection arranges, the top of described A reactor arranges material inlet, and the bottom of second reactor arranges material outlet; Described one-level, second reactor are calandria type fixed bed reactor.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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CN 201220236208 CN202638397U (en) | 2012-05-24 | 2012-05-24 | 1,4-cyclohexanedicarboxylates continuous fixed bed reactor |
Applications Claiming Priority (1)
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CN 201220236208 CN202638397U (en) | 2012-05-24 | 2012-05-24 | 1,4-cyclohexanedicarboxylates continuous fixed bed reactor |
Publications (1)
Publication Number | Publication Date |
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CN202638397U true CN202638397U (en) | 2013-01-02 |
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CN 201220236208 Expired - Lifetime CN202638397U (en) | 2012-05-24 | 2012-05-24 | 1,4-cyclohexanedicarboxylates continuous fixed bed reactor |
Country Status (1)
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110437067A (en) * | 2018-05-02 | 2019-11-12 | 湖南长岭石化科技开发有限公司 | The method for preparing cyclohexane cyclohexanedimethanodibasic ester |
CN110498742A (en) * | 2018-05-17 | 2019-11-26 | 中国石油化工股份有限公司 | A kind of phthalic acid ester hydrogenation technique |
CN116640059A (en) * | 2022-02-15 | 2023-08-25 | 中国石油化工股份有限公司 | A kind of process method of DINP hydrogenation to DINCH with two reactors connected in series |
-
2012
- 2012-05-24 CN CN 201220236208 patent/CN202638397U/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110437067A (en) * | 2018-05-02 | 2019-11-12 | 湖南长岭石化科技开发有限公司 | The method for preparing cyclohexane cyclohexanedimethanodibasic ester |
CN110498742A (en) * | 2018-05-17 | 2019-11-26 | 中国石油化工股份有限公司 | A kind of phthalic acid ester hydrogenation technique |
CN116640059A (en) * | 2022-02-15 | 2023-08-25 | 中国石油化工股份有限公司 | A kind of process method of DINP hydrogenation to DINCH with two reactors connected in series |
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Legal Events
Date | Code | Title | Description |
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C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CX01 | Expiry of patent term | ||
CX01 | Expiry of patent term |
Granted publication date: 20130102 |