CN202054765U - Propene carbonate synthesizing device - Google Patents
Propene carbonate synthesizing device Download PDFInfo
- Publication number
- CN202054765U CN202054765U CN2011201268160U CN201120126816U CN202054765U CN 202054765 U CN202054765 U CN 202054765U CN 2011201268160 U CN2011201268160 U CN 2011201268160U CN 201120126816 U CN201120126816 U CN 201120126816U CN 202054765 U CN202054765 U CN 202054765U
- Authority
- CN
- China
- Prior art keywords
- propylene carbonate
- tubular reactor
- crude product
- built
- propene carbonate
- 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 - Fee Related
Links
- SIXOAUAWLZKQKX-UHFFFAOYSA-N carbonic acid;prop-1-ene Chemical compound CC=C.OC(O)=O SIXOAUAWLZKQKX-UHFFFAOYSA-N 0.000 title abstract 3
- 230000002194 synthesizing effect Effects 0.000 title abstract 3
- 238000001816 cooling Methods 0.000 claims abstract description 11
- 239000012043 crude product Substances 0.000 claims abstract description 10
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 claims description 23
- 229910001220 stainless steel Inorganic materials 0.000 claims description 3
- 239000010935 stainless steel Substances 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 description 9
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 5
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 5
- 235000011089 carbon dioxide Nutrition 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 206010053615 Thermal burn Diseases 0.000 description 3
- 230000004913 activation Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Images
Landscapes
- Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)
Abstract
The utility model discloses a propene carbonate synthesizing device, which comprises a tubular reactor (1), a crude product buffer tank (4) and a crude product storage tank (5), wherein a built-in snakelike tubular heat exchanger (2) is arranged in a preheating cooling region in the tubular reactor (1) and is connected with a heat exchange medium switching device (3). The propene carbonate synthesizing device has the advantages that the problems of large occupied space, complicated pipelines, poor safety and the like of an external heat exchanger can be effectively solved, in addition, the occurrence of staff scalding accidents can be effectively avoided, and the operation is convenient.
Description
Technical field
The utility model relates to a kind of chemical industry synthesizer, especially a kind of propylene carbonate synthesizer.
Background technology
Reactor is a kind of equipment more special in the chemical industry equipment field, and its structure can vary because of the difference of response characteristic, and its performance quality directly has influence on the output and the quality of product.
It is generally acknowledged that the propylene carbonate synthesis mode is such, propylene oxide under certain temperature, pressure and catalyzer condition with the carbonic acid gas generation propylene carbonate that reacts.This reaction is a thermopositive reaction, and reaction heat 23KCal/mol this shows, take away the part heat from reactive system is favourable to the reaction that generates propylene carbonate in good time.Therefore, it is necessary in reactive system refrigerating unit being installed.
At present, the synthesizer of propylene carbonate adopts tubular reactor more, and the feed way of reactor and temperature control method are different, but the external heat exchanger regulating and controlling temperature of reactor that adopts more.The drawback of external heat exchanger is to take certain space, the pipeline complexity, and valve is many, and the leak point is many, complex operation.In addition, external heat exchanger outside temperature during operation is very high, causes operator's scald accident easily.
The utility model content
The technical problems to be solved in the utility model provides a kind of propylene carbonate synthesizer, can effectively solve external heat exchanger many, the problems such as pipeline is complicated, poor stability that take up room, and can effectively avoid taking place employee's scald accident, and is easy to operate.
In order to solve the problems of the technologies described above, propylene carbonate synthesizer of the present utility model, comprise tubular reactor, crude product surge tank and crude product storage tank, preheating cooling zone in the described tubular reactor is provided with built-in coiled interchanger, and built-in coiled interchanger is connected with the heat transferring medium shifter.
Adopt such propylene carbonate synthesizer, raw material propylene oxide and catalyzer are used the incoming stock region of activation of pump delivery from reactor head; The raw material liquid carbonic acid gas enters reaction with pump delivery and generates the district from reactor; Generate the district in reaction, under certain pressure, temperature and catalyzer condition, propylene oxide and the carbonic acid gas generation propylene carbonate that reacts produces a large amount of heats; The hot mixture that is rich in propylene carbonate enters the preheating cooling zone, obtains cooling to a certain degree under the cooling of built-in coiled interchanger, has avoided the propylene carbonate pyrolytic decomposition that generates timely and effectively.Simultaneously, propylene carbonate synthesizer of the present utility model also has less investment, advantages such as occupation of land is little, efficient is high, security height, and can effectively avoid taking place employee's scald accident.
As further improvement of the utility model, built-in coiled interchanger is made with stainless steel in the propylene carbonate synthesizer, avoids having improved integral production efficient because of interchanger is needed frequent break-down maintenance by dielectric corrosion with this.
Description of drawings
Fig. 1 is the structural representation of propylene carbonate synthesizer of the present utility model.
Embodiment
Below in conjunction with accompanying drawing embodiment of the present utility model is elaborated.
Fig. 1 shows concrete structure of the present utility model.Propylene carbonate synthesizer of the present utility model is made up of tubular reactor 1, built-in coiled interchanger 2, heat transferring medium shifter 3, crude product surge tank 4, crude product storage tank 5.Tubular reactor 1 is divided into three zones: raw material region of activation, reaction generate district, preheating cooling zone; Built-in coiled interchanger 2 usefulness stainless steels are made, and are installed in the preheating cooling zone of tubular reactor 1.Built-in coiled interchanger 2 is connected with heat transferring medium shifter 3.Raw material propylene oxide and catalyzer are used the incoming stock region of activation of pump delivery from tubular reactor 1 top; The raw material liquid carbonic acid gas enters reaction from tubular reactor 1 middle and lower part with pump delivery and generates the district; Generate the district in reaction, under certain pressure, temperature and catalyzer condition, propylene oxide and the carbonic acid gas generation propylene carbonate that reacts produces a large amount of heats; The hot mixture that is rich in propylene carbonate enters the preheating cooling zone, obtains cooling to a certain degree under the cooling of built-in coiled interchanger 2, has avoided the propylene carbonate pyrolytic decomposition of generation and the carrying out of other side reactions timely and effectively; Be rich in the bottom discharge of the mixture of propylene carbonate, be transported to crude product storage tank 5 through crude product surge tank 4 from tubular reactor 1, at last by pump delivery to the propylene carbonate refining system.
Claims (2)
1. propylene carbonate synthesizer, comprise tubular reactor (1), crude product surge tank (4) and crude product storage tank (5), it is characterized in that: the preheating cooling zone in the described tubular reactor (1) is provided with built-in coiled interchanger (2), and built-in coiled interchanger (2) is connected with heat transferring medium shifter (3).
2. according to the described propylene carbonate synthesizer of claim 1, it is characterized in that: built-in coiled interchanger (2) is made with stainless steel.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2011201268160U CN202054765U (en) | 2011-04-27 | 2011-04-27 | Propene carbonate synthesizing device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2011201268160U CN202054765U (en) | 2011-04-27 | 2011-04-27 | Propene carbonate synthesizing device |
Publications (1)
Publication Number | Publication Date |
---|---|
CN202054765U true CN202054765U (en) | 2011-11-30 |
Family
ID=45014746
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2011201268160U Expired - Fee Related CN202054765U (en) | 2011-04-27 | 2011-04-27 | Propene carbonate synthesizing device |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN202054765U (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111013496A (en) * | 2019-12-27 | 2020-04-17 | 江苏奥克化学有限公司 | Packed tower reactor for producing cyclic carbonate and production method |
-
2011
- 2011-04-27 CN CN2011201268160U patent/CN202054765U/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111013496A (en) * | 2019-12-27 | 2020-04-17 | 江苏奥克化学有限公司 | Packed tower reactor for producing cyclic carbonate and production method |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN102942953B (en) | Method for controlling catalyst and heating and cooling regenerant in reaction zone | |
CN102675035B (en) | Method for preparing vinyl chloride from acetylene and dichloroethane | |
CN102671580B (en) | A kind of axially successively increment type cold shock formula preparing propylene from methanol fixed bed reactors | |
CN104629842A (en) | Method and equipment for deoxidizing low-concentration oxygen-containing coal bed gas | |
CN104557571A (en) | Method of producing ethanolamine from liquid ammonia | |
CN101108790B (en) | Method for manufacturing dimethyl ether with solid acid catalysis methanol dehydration reaction | |
CN101092331A (en) | Method for synthesizing alkyl phenol by fixed bed | |
CN202054765U (en) | Propene carbonate synthesizing device | |
CN202666813U (en) | Axially layer by layer progressively increased chilled methanol to propylene (MTP) fixed bed reactor | |
CN210065595U (en) | Device for oxidative coupling of methane | |
CN102617296B (en) | On-line agent changing method of methyl tert-butyl ether (MTBE) expanded bed reactor | |
CN208414288U (en) | A kind of differential pressure thermocouple propylene refining separation system in production of propylene oxide | |
CN104152198A (en) | Methanation reaction process | |
CN105218309A (en) | Produce the method for ethylene glycol | |
CN203508023U (en) | Production device adopting gas-liquid mixing tubular cooling reaction for preparing glyoxylic acid | |
CN206027660U (en) | In succession quick reaction unit of liquid and liquid | |
CN104892400A (en) | Intermittent reaction-continuous reaction rectification combined process for catalytic synthesis of oxalic acid | |
CN108586185A (en) | A kind of differential pressure thermocouple propylene refining piece-rate system and separation method | |
CN101244996B (en) | Vertical type bubbling oxidation reaction device for synthesizing naphthalic acid | |
CN202715401U (en) | Fixed bed catalytic reaction device capable of adjusting temperature of material at inlet | |
CN105368514B (en) | Produce the method and device of synthetic natural gas | |
CN101851152A (en) | Method for preparing dimethyl ether by methyl alcohol gaseous phase dehydration | |
CN203170305U (en) | Combined-heat-exchange multi-shell-side fixed bed production equipment for preparing olefin from methanol | |
CN202590786U (en) | Reaction kettle with double coiled pipes | |
CN202621148U (en) | Gas-phase medium distributing device with stirring jade glass synthetic reaction kettle |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
C56 | Change in the name or address of the patentee | ||
CP01 | Change in the name or title of a patent holder |
Address after: 244000 Anhui city of Tongling Province Lake Road six Tongling nonferrous circular economy industrial park Patentee after: TONGLING JINTAI CHEMICAL INDUSTRIAL CO., LTD. Address before: 244000 Anhui city of Tongling Province Lake Road six Tongling nonferrous circular economy industrial park Patentee before: Tongling Jintai Chemical Industrial Co., Ltd. |
|
CF01 | Termination of patent right due to non-payment of annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20111130 Termination date: 20190427 |