CN1740125A - Method of preventing and eliminating discolor of 3-chloropropylene - Google Patents
Method of preventing and eliminating discolor of 3-chloropropylene Download PDFInfo
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- CN1740125A CN1740125A CN 200410046705 CN200410046705A CN1740125A CN 1740125 A CN1740125 A CN 1740125A CN 200410046705 CN200410046705 CN 200410046705 CN 200410046705 A CN200410046705 A CN 200410046705A CN 1740125 A CN1740125 A CN 1740125A
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- product
- chlorallylene
- add
- compound
- variable color
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Abstract
The method of preventing and eliminating discolor of 3-chloropropylene product is to add proper amount of compound containing epoxy radical during or after 3-chloropropylene producing process, so as to eliminate free acid from the product and convert Fe ion, Cr ion, Ni ion and other metal ions generated in acid corrosion into colorless complex. The added compound containing epoxy radical has very small amount and thus no influence on the product performance and application.
Description
Technical field
The present invention relates to a kind of method that prevents and eliminate the variable color of chlorallylene product.
Background technology
Purified chlorallylene product should be colourless.If but the Fe in the chlorallylene product
3+, Fe
2+, Cr
3+, Ni
2+The plasma amount is higher, then this product (0 ℃～40 ℃) very easily variable color at normal temperatures.Generally in fortnight, become yellow, yellow-green colour, red-brown, brownish black etc.Learn by literature search, " a kind of method that solves the chlorallylene variable color " patent application that the applicant proposed on October 20th, 2000 (the application number is: 001266438), and main water free acid and the metal Fe in the flush away chlorallylene product as far as possible that be stressed that
2+And Fe
2+With formed colored complex of chlorallylene etc.Though it is good that this method solves chlorallylene product color changeable effect, but need wash product with a certain amount of water, soft water or deionized water, workload is bigger, increase certain washing equipment investment and this method and cause the product moisture rising to influence the Application Areas of product; (the application number is: 01114409.2) in " a kind of method that suppresses and eliminate the chlorallylene variable color " patent application that the applicant proposed in 04 month 10 days calendar year 2001, a kind of excessive carbonate that adds in the chlorallylene product is provided, has eliminated free acid, Fe in the chlorallylene product
2+With colored title complex [Fe (H
2O)
m(3AC)
n]
2+Suppress and eliminate the method for chlorallylene variable color.But this method such as the solid-state carbonate of direct adding, not only reinforced operation inconvenience, the deposition of excess amount of solid carbonate in pipeline or basin that does not react away simultaneously can influence the packing of normal production and product; As add the aqueous solution of carbonate, then increased the isolating workload of profit two-phase, the propenyl chloride carried secretly away of the isolated aqueous phase rising that can cause device to consume simultaneously.Not in place as profit two-phase mask work, then very easily causing product moisture to rise influences the Application Areas of product.
Summary of the invention
The purpose of this invention is to provide a kind of workable, method that reaction effect better prevented and eliminated the variable color of chlorallylene product.
Chlorallylene is to carry out the high temperature substitution reaction by raw material propylene according to a certain ratio through preheating and raw material chlorine, the mixture that reaction generates obtains thick muriate through cooling and rough segmentation, thick muriate makes the HCl that contains in the thick muriate be removed substantially, obtain after taking off heavily through taking off light processing.The chlorallylene for preparing so still contains the HCl of trace, and its content is 10mgHCl/Kg
Chlorallylene～200mgHCl/Kg
Chlorallylene, make the variable color of chlorallylene product easily in storage, use.
The present invention utilizes the compound contain epoxide group and the free HCl reaction in the chlorallylene product to reduce free acid value and and the Fe that generates because of acid corrosion
3+, Fe
2+, Cr
3+, Ni
2+Plasma reaction generates colourless complex compound, thereby prevents and eliminate the variable color of chlorallylene product.The compound that wherein contains epoxide group is meant: molecular formula is C
nH
2nThe epoxy alkane of O, 2≤n≤6; Or molecular formula is C
nH
2n-2The oxirane ring alkane of O, 4≤n≤6; Or molecular formula is RC
nH
2n-n-1The halogenated epoxy alkane of O, 3≤n≤6, R refers to halogen element, and halogeno-group and epoxy group(ing) dystopy; Or any two or more mixture in the above-mentioned substance.
In order to achieve the above object, the present invention adopts following technical scheme:
Add an amount of compound that contains epoxide group in the preparation process of chlorallylene product or in the chlorallylene finished product, its add-on is 0.05 ‰～5.0 ‰ of a chlorallylene weight, stirs or shakes, and leaves standstill then; The stirring or the time of shaking generally were not less than 1 minute; Time of repose can be eliminated the free acid in the chlorallylene product more than 0.5 hour; Time of repose can make the Fe that generates because of acid corrosion more than 24 hours
3+, Fe
2+, Cr
3+, Ni
2+Be converted into colourless complex compound Deng metal ion.
The detailed technical scheme of the present invention is:
In the preparation process of chlorallylene product or in the chlorallylene finished product that does not have variable color, add the compound that contains epoxide group, the add-on that wherein contains the compound of epoxide group is 0.05 ‰～5.0 ‰ of a chlorallylene weight, eliminate the free acid in the chlorallylene product, prevent from storage, transportation, to contain Fe in the product system because of acid corrosion causes
3+, Fe
2+, Cr
3+, Ni
2+Deng metal ion, and then prevent the variable color of chlorallylene product.
Add the compound that contains epoxide group in the chlorallylene product of variable color, the add-on that wherein contains the compound of epoxide group is 0.05 ‰～5.0 ‰ of a chlorallylene weight, makes the Fe that contains in the chlorallylene product
3+, Fe
2+, Cr
3+, Ni
2+Be converted into colourless complex compound Deng metal ion, thereby product is become colorless; Eliminate the free acid in the chlorallylene product simultaneously, prevent from storage, transportation, to contain Fe in the product system because of acid corrosion causes
3+, Fe
2+, Cr
3+, Ni
2+Deng metal ion, reach the purpose that prevents and eliminate the variable color of chlorallylene product.
It is better than adding other compound effects that contain epoxide group to add propylene oxide.Raw material is easy to get because propylene oxide not only has, moderate cost, and the Fe that contains in easier and the chlorallylene
3+, Fe
2+, Cr
3+, Ni
2+Generate colourless complex compound Deng the metal ion reaction.
The present invention has following technique effect:
1, the chlorallylene product that utilizes the present invention to prepare, appearance colorless is transparent, and colourity is less than APHA20
#, the HCl content in the product is lower than 10mgHCl/Kg
Chlorallylene, at room temperature airtight storage more than 1 year product color do not change; Utilize the present invention to handle the APHA color of variable color number greater than 80
#The chlorallylene product, product color was reduced to below the 20# after 24 hours, the HCl content in the product is lower than 10mgHCl/Kg
Chlorallylene, at room temperature airtight storage more than 1 year product color do not change.
2, the present invention is workable, and the compound amount that contains epoxide group of adding is little, and the performance of product is not had influence, can not reduce the grade of product, can not influence the Application Areas of product.
3, the chlorallylene product of the variable color of handling through the present invention can make product up-gradation sell, for manufacturer creates more economic benefit.
Embodiment
Below the present invention is done to describe further by concrete exemplifying embodiment:
Embodiment 1: add a certain amount of propylene oxide equably in the cat head chlorallylene discharge nozzle after thick muriate takes off heavily processing, its add-on is 0.05 ‰ (weight) of chlorallylene discharging flow, leaves standstill to deposit after 8 hours therefrom sampling analysis in finished product storage tank again.The chlorallylene product of producing is a water white transparency, and colourity is less than APHA20
#, the acidity of free acid (in HCl) does not reduce to 0.0003% by 0.013% (the tower top outlet sampling adds propylene oxide), and the sample of this product keeps at room temperature airtight storage not variable color after 1 year.
Embodiment 2: add a certain amount of epoxy cyclohexane equably in the cat head chlorallylene discharge nozzle after thick muriate takes off heavily processing, its add-on is 0.5 ‰ (weight) of chlorallylene discharging flow, leaves standstill to deposit after 8 hours therefrom sampling analysis in finished product storage tank again.The chlorallylene product of producing is a water white transparency, and colourity is less than APHA20
#, the acidity of free acid (in HCl) does not reduce to 0.0002% by 0.018% (the tower top outlet sampling adds epoxy cyclohexane), and the sample of this product keeps at room temperature airtight storage not variable color after 1 year.
Embodiment 3: add a certain amount of epoxy chloropropane equably in the cat head chlorallylene discharge nozzle after thick muriate takes off heavily processing, its add-on is 0.1 ‰ (weight) of chlorallylene discharging flow, leaves standstill to deposit after 8 hours therefrom sampling analysis in finished product storage tank again.The chlorallylene product of producing is a water white transparency, and colourity is less than APHA20
#, the acidity of free acid (in HCl) does not reduce to 0.0004% by 0.012% (the tower top outlet sampling adds epoxy cyclohexane), and the sample of this product keeps at room temperature airtight storage not variable color after 1 year.
Embodiment 4: add the mixture (both mass ratioes are 1: 1) of 12kg propylene oxide and epoxy cyclohexane in the storage tank of the chlorallylene product that about 60000kg band Sandy is housed after, mixed 15 minutes by the recycle pump circulation, leave standstill after 0.5 hour therefrom sampling analysis, the acidity of free acid (in HCl) by 0.01% (add the mixture of propylene oxide and epoxy cyclohexane before sampling analysis) reduce to 0.0005%; Left standstill 24 hours, this product becomes colourity less than APHA20 by Sandy
#Colourless transparent liquid, and with the at room temperature airtight preservation of the sample of this product not variable color again after 1 year.
Embodiment 5: add the mixture (both mass ratioes are 2: 1) of 300kg propylene oxide and epoxy cyclohexane in the storage tank of the chlorallylene product that about 60000kg band Sandy is housed after, mixed 15 minutes by the recycle pump circulation, leave standstill after 2 hours therefrom sampling analysis, the acidity of free acid (in HCl) by 0.018% (add the mixture of propylene oxide and epoxy cyclohexane before sampling analysis) reduce to 0.0004%; Left standstill 24 hours, this product becomes colourity less than APHA20 by Sandy
#Colourless transparent liquid, and with the at room temperature airtight preservation of the sample of this product not variable color again after 1 year.
Embodiment 6: in the storage tank of the chlorallylene product that about 60000kg band Sandy is housed, add 90kg oxyethane, propylene oxide, epoxy cyclohexane mixture (because of the oxyethane boiling point low, so operation when being chosen in room temperature and being 4 ℃, three's mass ratio is 1: 1: 1) after, mixed 15 minutes by the recycle pump circulation, leave standstill after 1.5 hours therefrom sampling analysis, the acidity of free acid (in HCl) by 0.018% (add the mixture of oxyethane, propylene oxide, epoxy cyclohexane before sampling analysis) reduce to 0.0004%; Left standstill 24 hours, this product becomes colourity less than APHA20 by Sandy
#Colourless transparent liquid, and with the at room temperature airtight preservation of the sample of this product not variable color again after 1 year.
Embodiment 6: add 90kg propylene oxide, epoxy cyclohexane, epoxy chloropropionate alkylating mixture (three's mass ratio is 1: 1: 1) in the storage tank of the chlorallylene product that about 60000kg band Sandy is housed after, mixed 15 minutes by the recycle pump circulation, leave standstill after 1.5 hours therefrom sampling analysis, the acidity of free acid (in HCl) by 0.016% (add the mixture of oxyethane, propylene oxide, epoxy cyclohexane before sampling analysis) reduce to 0.0003%; Left standstill 24 hours, this product becomes colourity less than APHA20 by Sandy
#Colourless transparent liquid, and with the at room temperature airtight preservation of the sample of this product not variable color again after 1 year.
Embodiment 7: in two volumes all are 200 liters metal bucket, after adding the chlorallylene product of the temporary transient appearance colorless of 180kg simultaneously respectively, add 45 gram propylene oxide, 45 gram epoxy cyclohexanes more respectively, shook metal bucket 5 minutes, leave standstill and preserve sampling analysis after month, colourity is all still less than APHA20
#The acidity of free acid (in HCl) is respectively 0.0006%, 0.0008%, and for the chlorallylene that does not have to add the compound treatment that contains epoxide group that is placed on the same quality in another metal bucket, chlorallylene product after 24 hours in this bucket has become red-brown, and the acidity of the free acid in the product is 0.005% after tested.
Claims (2)
1, a kind of method that prevents and eliminate the variable color of chlorallylene product, it is characterized in that: in the preparation process of chlorallylene product or in the chlorallylene finished product, add an amount of compound that contains epoxide group, its add-on is 0.05 ‰～5.0 ‰ of a chlorallylene weight, stir or shake, leave standstill then; The stirring or the time of shaking generally were not less than 1 minute; Time of repose can be eliminated the free acid in the chlorallylene product more than 0.5 hour; Time of repose can make the Fe that generates because of acid corrosion more than 24 hours
3+, Fe
2+, Cr
3+, Ni
2+Be converted into colourless complex compound Deng metal ion; The compound that wherein contains epoxide group is meant: molecular formula is C
nH
2nThe epoxy alkane of O, 2≤n≤6; Or molecular formula is C
nH
2n-2The oxirane ring alkane of O, 4≤n≤6; Or molecular formula is RC
nH
2n-1The halogenated epoxy alkane of O, 3≤n≤6, R refers to halogen element, and halogeno-group and epoxy group(ing) dystopy; Or any two or more mixture in the above-mentioned substance.
2, method according to claim 1, the compound that it is characterized in that containing epoxide group is a propylene oxide.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2004100467053A CN1307136C (en) | 2004-08-24 | 2004-08-24 | Method of preventing and eliminating discolor of 3-chloropropylene |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2004100467053A CN1307136C (en) | 2004-08-24 | 2004-08-24 | Method of preventing and eliminating discolor of 3-chloropropylene |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1740125A true CN1740125A (en) | 2006-03-01 |
| CN1307136C CN1307136C (en) | 2007-03-28 |
Family
ID=36092680
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2004100467053A Expired - Fee Related CN1307136C (en) | 2004-08-24 | 2004-08-24 | Method of preventing and eliminating discolor of 3-chloropropylene |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1307136C (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8858820B2 (en) | 2011-10-07 | 2014-10-14 | American Pacific Corporation | Bromofluorocarbon compositions |
| CN105859509A (en) * | 2016-04-14 | 2016-08-17 | 中国科学院化学研究所 | Chloropropene purifying method and application thereof |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3825380A (en) * | 1972-07-07 | 1974-07-23 | Exxon Research Engineering Co | Melt-blowing die for producing nonwoven mats |
| JP2813100B2 (en) * | 1992-10-23 | 1998-10-22 | 株式会社トクヤマ | Method and apparatus for producing allyl chloride |
| US5618984A (en) * | 1994-06-24 | 1997-04-08 | Mitsui Toatsu Chemicals, Inc. | Phenol aralkyl resins, preparation process thereof and epoxy resin compositions |
-
2004
- 2004-08-24 CN CNB2004100467053A patent/CN1307136C/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8858820B2 (en) | 2011-10-07 | 2014-10-14 | American Pacific Corporation | Bromofluorocarbon compositions |
| CN105859509A (en) * | 2016-04-14 | 2016-08-17 | 中国科学院化学研究所 | Chloropropene purifying method and application thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1307136C (en) | 2007-03-28 |
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| PB01 | Publication | ||
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| C14 | Grant of patent or utility model | ||
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Owner name: CHINA PETROCHEMICAL CORPORATION; BALING PETROCHEM Free format text: FORMER OWNER: BALING PETROCHEMICAL CO., LTD., SINOPEC Effective date: 20070615 |
|
| C41 | Transfer of patent application or patent right or utility model | ||
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Effective date of registration: 20070615 Address after: 100029 No. 6, Xin Xin Street East, Beijing, Chaoyang District Co-patentee after: Baling Petrochemical Co., Ltd., SINOPEC Patentee after: China Petrochemical Group Corp. Address before: 414014 Yunxi District, Hunan, Yueyang Patentee before: Baling Petrochemical Co., Ltd., SINOPEC |
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| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20070328 Termination date: 20180824 |
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| CF01 | Termination of patent right due to non-payment of annual fee |