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CN105111166A - Sulfonation reaction cooling method in acesulfame synthesis technology - Google Patents

Sulfonation reaction cooling method in acesulfame synthesis technology Download PDF

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Publication number
CN105111166A
CN105111166A CN201510517561.3A CN201510517561A CN105111166A CN 105111166 A CN105111166 A CN 105111166A CN 201510517561 A CN201510517561 A CN 201510517561A CN 105111166 A CN105111166 A CN 105111166A
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CN
China
Prior art keywords
cooling
sulfonation
sulfonation reaction
liquid ammonia
brine
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.)
Pending
Application number
CN201510517561.3A
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Chinese (zh)
Inventor
王从春
祁飞
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Anhui Jinhe Industrial Co Ltd
Original Assignee
Anhui Jinhe Industrial Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Anhui Jinhe Industrial Co Ltd filed Critical Anhui Jinhe Industrial Co Ltd
Priority to CN201510517561.3A priority Critical patent/CN105111166A/en
Publication of CN105111166A publication Critical patent/CN105111166A/en
Pending legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D291/00Heterocyclic compounds containing rings having nitrogen, oxygen and sulfur atoms as the only ring hetero atoms
    • C07D291/02Heterocyclic compounds containing rings having nitrogen, oxygen and sulfur atoms as the only ring hetero atoms not condensed with other rings
    • C07D291/06Six-membered rings
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/10Process efficiency

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention discloses a sulfonation reaction cooling method in an acesulfame synthesis technology. The method is characterized in that liquid ammonia is adopted to replace copious cooling brine and enters a heat exchanger as a cooling agent to directly cool a sulfonation kettle, and the temperature in the sulfonation kettle is controlled by regulating the flow of the liquid ammonia so as to meet the temperature requirement of sulfonation reaction. The method has the advantages that based on the characteristics of low specific gravity and low boiling point of the liquid ammonia, heat generated in sulfonation reaction is taken away through sublimation of the liquid ammonia so as to achieve cooling. Compared with an existing cooling method, restrictions on production from brine pumps are eliminated, the usage quantity of brine pumps is reduced, and a large amount of electric energy is saved; the purchase and installation cost and the repair and maintenance cost of brine tanks and dry evaporative cooling equipment are lowered, annual calcium chloride consumption and soft water consumption are reduced, and influences on the environment in the overhaul process are eliminated.

Description

Sulfonation reaction method of cooling in a kind of acesulfame potassium synthesis technique
Technical field
The present invention relates to acesulfame potassium synthesis technique field, particularly sulfonation reaction method of cooling in a kind of acesulfame potassium synthesis technique.
Background technology
Sulfonation workshop section, as the main workshop section affecting acesulfame potassium yield, wants less than-30 DEG C to carry out just guaranteeing that reaction is carried out smoothly in this workshop section's reaction needed.Traditional acesulfame potassium production technique sulfonation workshop section as shown in Figure 1, temperature in the kettle is controlled with deep cooling salt solution (calcium chloride solution of more than 30%) cooling, deep cooling salt solution enters interchanger by brinepump, in control process, cold damage is large, indirect control is unfavorable for producing adjustment, affects greatly by brinepump efficiency.This project utilizes liquefied ammonia proportion low, low-boiling feature, directly to sulphonation kettle cooling, eliminate brinepump to the restriction of producing, decrease the use of pump simultaneously, reduce equipment maintenance expense, simultaneously due to direct cooling, cold damage is little, stops 250KW ice maker one, more eliminate the pollution of deep cooling salt solution to environment, the target level of product quality of chemical industry can be reached completely.
Summary of the invention
The cold damage of control process is there is large for the prior art type of cooling, affect large shortcoming by brinepump efficiency, the invention provides sulfonation reaction method of cooling in a kind of acesulfame potassium synthesis technique, eliminate brinepump to the restriction of producing, reduce the use of brinepump, save a large amount of electric energy.
The object of the invention is to be achieved by the following technical programs, sulfonation reaction method of cooling in a kind of acesulfame potassium synthesis technique, it is characterized in that, adopt liquefied ammonia to replace deep cooling salt solution to enter interchanger as refrigerant directly to lower the temperature to sulphonation kettle, control sulfonation temperature in the kettle to meet the temperature requirement of sulfonation reaction by regulator solution ammonia flow.
Beneficial effect: by utilizing liquefied ammonia proportion low, low-boiling feature, takes away the heat of sulfonation reaction by the distillation of liquefied ammonia, reach the object of cooling.Compared with existing method of cooling, this invention removes brinepump to the restriction of producing, reduce the use of brinepump, save a large amount of electric energy.Reduce the equipment purchasing installation costs maintenance expense of salt water tank and dry type evaporating cold, decrease the annual calcium chloride of consumption and the use of soft water, eliminate the impact on environment in maintenance process.
Accompanying drawing explanation
Fig. 1 is sulfonation reaction schema in existing acesulfame potassium synthesis technique;
Fig. 2 is sulfonation reaction schema in acesulfame potassium synthesis technique of the present invention.
Embodiment
As shown in Figure 2, the invention provides sulfonation reaction method of cooling in a kind of acesulfame potassium synthesis technique, utilize liquefied ammonia proportion low, low-boiling feature, the heat of sulfonation reaction is taken away by the distillation of liquefied ammonia, reach the object of cooling, the deep cooling salt solution adopting liquefied ammonia to replace tradition to use enters interchanger as refrigerant and directly lowers the temperature to sulphonation kettle, controls sulfonation temperature in the kettle to meet the temperature requirement of sulfonation reaction by regulator solution ammonia flow.
Concrete operation step:
1) open sulfonation recycle pump, make material enter heat exchanger tube pass;
2) open ice maker, open evaporative condenser, open and add ammonia valve, make liquefied ammonia enter interchanger;
3) distribute cylinder regulator solution ammonia flow by ammonia and control sulphonation kettle temperature;
4) start when reaching temperature of reaction-30 DEG C to drip, and distribute cylinder ammonia residual adjustment still temperature by ammonia.
This invention removes brinepump to the restriction of producing, reduce the use of brinepump, save a large amount of electric energy.
Above-described embodiment is as better embodiment of the present invention; describe technical conceive of the present invention and essential implementation in detail; not that protection scope of the present invention is limited; all any simple modification of doing according to spirit of the present invention and equivalent structure transformation or modification, all should be encompassed within protection scope of the present invention.

Claims (1)

1. sulfonation reaction method of cooling in an acesulfame potassium synthesis technique, it is characterized in that, adopt liquefied ammonia to replace deep cooling salt solution to enter interchanger as refrigerant directly to lower the temperature to sulphonation kettle, control sulfonation temperature in the kettle to meet the temperature requirement of sulfonation reaction by regulator solution ammonia flow.
CN201510517561.3A 2015-08-22 2015-08-22 Sulfonation reaction cooling method in acesulfame synthesis technology Pending CN105111166A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510517561.3A CN105111166A (en) 2015-08-22 2015-08-22 Sulfonation reaction cooling method in acesulfame synthesis technology

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510517561.3A CN105111166A (en) 2015-08-22 2015-08-22 Sulfonation reaction cooling method in acesulfame synthesis technology

Publications (1)

Publication Number Publication Date
CN105111166A true CN105111166A (en) 2015-12-02

Family

ID=54659320

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510517561.3A Pending CN105111166A (en) 2015-08-22 2015-08-22 Sulfonation reaction cooling method in acesulfame synthesis technology

Country Status (1)

Country Link
CN (1) CN105111166A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10023546B2 (en) 2016-09-21 2018-07-17 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10030000B2 (en) 2016-09-21 2018-07-24 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10029999B2 (en) 2016-09-21 2018-07-24 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10029998B2 (en) 2016-09-21 2018-07-24 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
CN108383816A (en) * 2018-01-13 2018-08-10 安徽金禾实业股份有限公司 A kind of method of maltol chlorination reaction heat exchange

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN202057108U (en) * 2011-03-29 2011-11-30 江苏嘉隆化工有限公司 Ammonia refrigeration device
EP2407146A1 (en) * 2010-07-15 2012-01-18 Nutrinova Nutrition Specialties & Food Ingredients GmbH Use of acesulfame K as a flavour modulator
CN103613566A (en) * 2013-11-01 2014-03-05 安徽金禾实业股份有限公司 Acesulfame potassium cyclization continuous production method

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2407146A1 (en) * 2010-07-15 2012-01-18 Nutrinova Nutrition Specialties & Food Ingredients GmbH Use of acesulfame K as a flavour modulator
CN202057108U (en) * 2011-03-29 2011-11-30 江苏嘉隆化工有限公司 Ammonia refrigeration device
CN103613566A (en) * 2013-11-01 2014-03-05 安徽金禾实业股份有限公司 Acesulfame potassium cyclization continuous production method

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
王壮坤: "《流体输送与传热技术》", 30 September 2009 *
黄林峰: "安赛蜜工厂工艺流程设计探讨", 《南昌大学硕士学位论文》 *

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10590095B2 (en) 2016-09-21 2020-03-17 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US11718594B2 (en) 2016-09-21 2023-08-08 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10029999B2 (en) 2016-09-21 2018-07-24 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10029998B2 (en) 2016-09-21 2018-07-24 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US11731948B2 (en) 2016-09-21 2023-08-22 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10208004B2 (en) 2016-09-21 2019-02-19 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10227316B2 (en) 2016-09-21 2019-03-12 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10233163B2 (en) 2016-09-21 2019-03-19 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10233164B2 (en) 2016-09-21 2019-03-19 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10590097B2 (en) 2016-09-21 2020-03-17 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10590098B2 (en) 2016-09-21 2020-03-17 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10590096B2 (en) 2016-09-21 2020-03-17 Celenese International Corporation Acesulfame potassium compositions and processes for producing same
US10030000B2 (en) 2016-09-21 2018-07-24 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10759771B2 (en) 2016-09-21 2020-09-01 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10023546B2 (en) 2016-09-21 2018-07-17 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10781190B2 (en) 2016-09-21 2020-09-22 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10781191B2 (en) 2016-09-21 2020-09-22 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10954204B2 (en) 2016-09-21 2021-03-23 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10954203B2 (en) 2016-09-21 2021-03-23 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10961207B2 (en) 2016-09-21 2021-03-30 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10975047B2 (en) 2016-09-21 2021-04-13 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US10759770B2 (en) 2016-09-21 2020-09-01 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US11724993B2 (en) 2016-09-21 2023-08-15 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
US11724994B2 (en) 2016-09-21 2023-08-15 Celanese International Corporation Acesulfame potassium compositions and processes for producing same
CN108383816A (en) * 2018-01-13 2018-08-10 安徽金禾实业股份有限公司 A kind of method of maltol chlorination reaction heat exchange

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Application publication date: 20151202

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