Nothing Special   »   [go: up one dir, main page]

CN106365952A - Method for solvent self-heating separation in acesulfame potassium synthesis - Google Patents

Method for solvent self-heating separation in acesulfame potassium synthesis Download PDF

Info

Publication number
CN106365952A
CN106365952A CN201610751007.6A CN201610751007A CN106365952A CN 106365952 A CN106365952 A CN 106365952A CN 201610751007 A CN201610751007 A CN 201610751007A CN 106365952 A CN106365952 A CN 106365952A
Authority
CN
China
Prior art keywords
kettle
temperature
reactor
solvent
condenser
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.)
Granted
Application number
CN201610751007.6A
Other languages
Chinese (zh)
Other versions
CN106365952B (en
Inventor
周睿
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 CN201610751007.6A priority Critical patent/CN106365952B/en
Publication of CN106365952A publication Critical patent/CN106365952A/en
Application granted granted Critical
Publication of CN106365952B publication Critical patent/CN106365952B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/38Separation; Purification; Stabilisation; Use of additives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/38Separation; Purification; Stabilisation; Use of additives
    • C07C17/383Separation; Purification; Stabilisation; Use of additives by distillation
    • 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

Landscapes

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

Abstract

The invention discloses a method for solvent self-heating separation in acesulfame potassium synthesis. The method includes the following steps of pumping solid potassium hydroxide and water of the conventional adding percents into a reactor to make potassium hydroxide and water dissolved in a neutralization kettle and release heat till the temperature is naturally raised to 60 DEG C, starting a vacuum pump connected with the neutralization kettle to vacuumize the neutralization kettle to the negative pressure of -0.4 MPa, pumping an organic phase of the conventional adding percent into the reactor to make the temperature in the kettle naturally decrease and then increase, starting the vacuum pump to conduct vacuumization till a condenser valve when the temperature of the kettle is raised to 50 DEG C, starting the condenser brine valve, controlling the temperature of the kettle at 45 DEG C by controlling the feeding ratio of the organic phase to sodium carbonate, and discharging condensed dichloromethane to a solvent collecting tank through a condenser. The method has the advantages that solvent is pressurized in the reactor and depressurized after getting out of the reactor, the boiling point of the solvent is reduced, original processes of separating, washing, separating, pre-boiling and the like are omitted through temperature control, operation is simplified, labor intensity is reduced, machines and pumps are less used, and meanwhile lots of steam is saved.

Description

Solvent self-heating separation method in a kind of acesulfame potassium synthesis
Technical field
The present invention relates to acesulfame potassium synthesis technique field, particularly a kind of acesulfame potassium synthesize in neutralization reaction from thermal release Method.
Background technology
At present in acesulfame potassium synthesis and production process, as shown in figure 1, neutralization dichloromethane separation phase complex process, be first By former dichloromethane with sugar and water mixture by separating through stratification, then proceed to organic faciess groove, then through washing, washing Stratification separates again afterwards, enters back into thick steaming, could use for rectification, not only needs in the process to add large number quipments, and And a large amount of loss of phase heat energy need to be taken away with saline before manufacture, the later stage needs to consume a large amount of steam, capacity usage ratio by heating Lowly, waste seriously.
Content of the invention
The purpose of the present invention is aiming in prior art isolation technics there is process complexity, and post operation step is many, machine The shortcoming that pump uses in a large number and steam usage amount is big, provides solvent self-heating separation method in a kind of acesulfame potassium synthesis.
The purpose of the present invention is achieved by the following technical programs:
Solvent self-heating separation method in a kind of acesulfame potassium synthesis, comprises the following steps:
1) solid potassium hydroxide of conventional proportions amount and water are first pumped into reactor, make their exothermic dissolutions in neutralization kettle natural It is warming up to 60 DEG C;
2) open the vacuum pump being connected with neutralization kettle, negative pressure -0.4mpa will be pumped in neutralization kettle;
3) organic faciess of conventional proportions amount are pumped in reactor, temperature in the kettle self-assembling formation first reduces and raises afterwards;
4) kettle temperature is increased to 50 DEG C, opens vacuum pump and is vented to condenser valve;
5) open condenser saline valve, by controlling the pan feeding ratio of organic faciess and soda, control kettle temperature at 45 DEG C;
6) condenser discharges the dichloromethane of condensation to solvent groove.
Technical scheme, using solid potassium hydroxide exothermic dissolution and neutralization reaction heat release, in the reactor plus Pressure, reduces pressure after going out reactor, reduces solvent boiling point, so that dichloromethane is being evaporated rapidly after reactor, through condensing back Receive and directly use for rectification.
The invention has the advantages that: solvent pressurizes in the reactor, reduce pressure after going out reactor, reduce solvent boiling point, pass through Temperature control, removes the processes such as original separation, washing, separation, pre- steaming, simplifies operation, reduce labor intensity, reduce pump Use, save a large amount of steam simultaneously.
Brief description
Fig. 1 is neutralization reaction solvent fractionation method flow chart in existing acesulfame potassium synthesis technique;
Fig. 2 neutralizes from hot solvent separation process figure in the acesulfame potassium synthesis technique of the present invention.
Specific embodiment
As shown in Fig. 2 the present invention provides solvent self-heating separation method in a kind of acesulfame potassium synthesis, using exothermic dissolution with instead Answer heat release, pressurize in the reactor, reduce pressure after going out reactor, reduce solvent boiling point, make dichloromethane after reactor Rapid evaporation, reclaims through condensation and replaces original standing separation, washing, the process such as separate, steam in advance again
Concrete operation step:
7) solid potassium hydroxide 0.6t/h and water 5t/h are first pumped into reactor, make neutralization kettle kettle temperature naturally rise to 60 DEG C.
8) open vacuum pump, negative pressure -0.4mpa will be pumped in neutralization kettle.
9) by organic faciess 10m3/ h pumps into temperature in the kettle in reactor first to be reduced and raises afterwards.
10) kettle temperature is increased to 50 DEG C, opens emptying to condenser valve.
11) open condenser saline valve, by controlling the organic faciess of organic faciess and the pan feeding ratio of soda, control kettle temperature to exist 45℃.
The present invention removes the processes such as original separation, washing, separation, pre- steaming, simplifies operation, reduces labor intensity.Reduce Ice maker and the use of pump, save a large amount of steam simultaneously.780,000 degree of estimated annual using electricity wisely, 4000 tons of annual steam saving.
Above-described embodiment, as the better embodiment of the present invention, is described in detail the technology design of the present invention and implements to want Point, is not that protection scope of the present invention is limited, all according to spirit of the invention made any simple modification and Equivalent structure transformation or modification, all should be included within the scope of the present invention.

Claims (1)

1. solvent self-heating separation method in a kind of acesulfame potassium synthesis, comprises the following steps:
The solid potassium hydroxide of conventional proportions amount and water are first pumped into reactor, so that their exothermic dissolutions in neutralization kettle is naturally risen Temperature is to 60 DEG C;
Open the vacuum pump being connected with neutralization kettle, negative pressure -0.4mpa will be pumped in neutralization kettle;
The organic faciess of conventional proportions amount are pumped in reactor, temperature in the kettle self-assembling formation first reduces and raises afterwards;
Kettle temperature is increased to 50 DEG C, opens vacuum pump and is vented to condenser valve;
Open condenser saline valve, by controlling the pan feeding ratio of organic faciess and soda, control kettle temperature at 45 DEG C;
Condenser discharges the dichloromethane of condensation to solvent groove.
CN201610751007.6A 2016-08-30 2016-08-30 Solvent self-heating separation method in a kind of synthesis of acesulfame potassium Active CN106365952B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610751007.6A CN106365952B (en) 2016-08-30 2016-08-30 Solvent self-heating separation method in a kind of synthesis of acesulfame potassium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610751007.6A CN106365952B (en) 2016-08-30 2016-08-30 Solvent self-heating separation method in a kind of synthesis of acesulfame potassium

Publications (2)

Publication Number Publication Date
CN106365952A true CN106365952A (en) 2017-02-01
CN106365952B CN106365952B (en) 2018-10-26

Family

ID=57903768

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610751007.6A Active CN106365952B (en) 2016-08-30 2016-08-30 Solvent self-heating separation method in a kind of synthesis of acesulfame potassium

Country Status (1)

Country Link
CN (1) CN106365952B (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
US10029998B2 (en) 2016-09-21 2018-07-24 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
CN109593071A (en) * 2018-12-10 2019-04-09 安徽金禾实业股份有限公司 A kind of continuous controllable acesulfame potassium recrystallization centrifugal device and method

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1680344A (en) * 2004-02-17 2005-10-12 大赛璐化学工业株式会社 Method for producing 3,4-dihydro-1,2,3-oxathiazin-4-one-2,2-dioxide compound or salt thereof
CN101787001A (en) * 2010-03-17 2010-07-28 广东省食品工业研究所 Synthesis process of acesulfame potassium
CN103588728A (en) * 2013-11-01 2014-02-19 安徽金禾实业股份有限公司 Neutralization direct crystallization production technology of acesulfame potassium
CN104411693A (en) * 2012-06-08 2015-03-11 鹿特诺瓦营养品和食品有限公司 Process for producing acesulfame potassium
CN105085160A (en) * 2015-08-22 2015-11-25 安徽金禾实业股份有限公司 Method for recycling dichloromethane in acesulfame potassium synthesis process

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1680344A (en) * 2004-02-17 2005-10-12 大赛璐化学工业株式会社 Method for producing 3,4-dihydro-1,2,3-oxathiazin-4-one-2,2-dioxide compound or salt thereof
CN101787001A (en) * 2010-03-17 2010-07-28 广东省食品工业研究所 Synthesis process of acesulfame potassium
CN104411693A (en) * 2012-06-08 2015-03-11 鹿特诺瓦营养品和食品有限公司 Process for producing acesulfame potassium
CN103588728A (en) * 2013-11-01 2014-02-19 安徽金禾实业股份有限公司 Neutralization direct crystallization production technology of acesulfame potassium
CN105085160A (en) * 2015-08-22 2015-11-25 安徽金禾实业股份有限公司 Method for recycling dichloromethane in acesulfame potassium synthesis process

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
冯锐等: "甜味剂安赛蜜的合成研究", 《四川师范学院学报(自然科学版)》 *
薛连海等: "安赛蜜生产控制分析方法的改进", 《滁州学院学报》 *

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10590096B2 (en) 2016-09-21 2020-03-17 Celenese 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
US10023546B2 (en) 2016-09-21 2018-07-17 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
US10759771B2 (en) 2016-09-21 2020-09-01 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
US10759770B2 (en) 2016-09-21 2020-09-01 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
US10590098B2 (en) 2016-09-21 2020-03-17 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
US10590095B2 (en) 2016-09-21 2020-03-17 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
US10029998B2 (en) 2016-09-21 2018-07-24 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
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
US10954203B2 (en) 2016-09-21 2021-03-23 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
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
US11718594B2 (en) 2016-09-21 2023-08-08 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
CN109593071A (en) * 2018-12-10 2019-04-09 安徽金禾实业股份有限公司 A kind of continuous controllable acesulfame potassium recrystallization centrifugal device and method

Also Published As

Publication number Publication date
CN106365952B (en) 2018-10-26

Similar Documents

Publication Publication Date Title
CN106365952A (en) Method for solvent self-heating separation in acesulfame potassium synthesis
CN104230136B (en) Sludge high temperature pyrohydrolysis combined vacuum flash-evaporation dehydration facture
CN102659196A (en) Energy-saving evaporation process and system thereof
CN102380226A (en) Acesulfame sugar water concentration method
CN103242384B (en) Mother liquor of sucralose extraction process
CN102491385A (en) Method for using dissolved exhaust steam in alumina production
CN105498260A (en) High-efficiency and energy-saving caprolactam recovery technology
CN103101932A (en) Comprehensive utilizing system for extracting salt from seawater, preparing drinking water and recovering power generation energy
CN103922529A (en) Low-energy-consumption device for recycling hydrochloric acid waste water and method for recycling hydrochloric acid waste water
CN103467245A (en) Method for complexing and removing water contained in ethanol and water mixed solution by utilizing eutectic solvent
CN101143730A (en) Method for producing salt by directly vacuum vaporizing bittern which is not being duplicate dried in field
CN104724776B (en) Devices and methods therefor in pressure evaporating indirect steam incorporation press water
CN213790069U (en) Novel plant extraction equipment
CN104548638B (en) Thermo-compression evaporation unit waste heat reclaiming process and device
CN111186950B (en) High-yield seawater desalination system and operation method
CN205402671U (en) Novel evaporate cauldron waste heat comprehensive recovery system that presses
CN104695921A (en) System for utilizing oil field produced wastewater to prepare high-dryness steam for steam flooding
CN106565812A (en) Efficient recovery process for tea saponin continuous extraction solvent
CN103007565B (en) Method and device for triple-effect separation of methylbenzene and polyethylene
CN213060771U (en) Processing and production system for extracting walnut oil
CN104587688B (en) Plant lixiviating solution negative pressure concentration systems
CN108955297A (en) Low-pressure steam and condensing hot air furnace method
CN102492555B (en) Method and device for high-efficiency energy-saving desolvation of fossilized animal/plant wax-containing solution
CN108211801A (en) A kind of multiple-effect distillation device, system and method
CN204447357U (en) Thermo-compression evaporation unit waste-heat recovery device

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant
PE01 Entry into force of the registration of the contract for pledge of patent right
PE01 Entry into force of the registration of the contract for pledge of patent right

Denomination of invention: Method for solvent self-heating separation in acesulfame potassium synthesis

Effective date of registration: 20191113

Granted publication date: 20181026

Pledgee: Bank of China Limited Chuzhou Branch

Pledgor: Anhui Jinhe Stock Co., Ltd.

Registration number: Y2019340000196

PC01 Cancellation of the registration of the contract for pledge of patent right
PC01 Cancellation of the registration of the contract for pledge of patent right

Date of cancellation: 20210115

Granted publication date: 20181026

Pledgee: Bank of China Limited Chuzhou Branch

Pledgor: ANHUI JINGHE INDUSTRIAL Co.,Ltd.

Registration number: Y2019340000196