CN102603668A - Method for treating 2-mercaptobenzothiazole production waste - Google Patents

Method for treating 2-mercaptobenzothiazole production waste Download PDF

Info

Publication number
CN102603668A
CN102603668A CN2012100399188A CN201210039918A CN102603668A CN 102603668 A CN102603668 A CN 102603668A CN 2012100399188 A CN2012100399188 A CN 2012100399188A CN 201210039918 A CN201210039918 A CN 201210039918A CN 102603668 A CN102603668 A CN 102603668A
Authority
CN
China
Prior art keywords
tower
mercaptobenzothiazole
distillation
rectifying
obtains
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
CN2012100399188A
Other languages
Chinese (zh)
Other versions
CN102603668B (en
Inventor
刘炤
阴自义
周现臣
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.)
Hebi Hengli Rubber Co ltd
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to CN2012100399188A priority Critical patent/CN102603668B/en
Publication of CN102603668A publication Critical patent/CN102603668A/en
Application granted granted Critical
Publication of CN102603668B publication Critical patent/CN102603668B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention discloses a method for treating 2-mercaptobenzothiazole production waste. The method comprises the steps of: heating the 2-mercaptobenzothiazole production waste to 90-95 DEG C, carrying out solid-liquid separation to obtain solid matter and liquid A, returning the solid matter to an accelerator M workshop, refining and purifying the solid matter to obtain a product accelerator M, distilling and separating the liquid A to obtain a fraction B and a fraction C, cooling residues in a distillation kettle to obtain asphalt-shaped matter D, absorbing hydrogen sulfide gas generated in the distillation separation process by using a sodium hydroxide solution to obtain a sodium hydrosulfide solution, concentrating the sodium hydrosulfide solution to obtain sodium hydrosulfide solids, rectifying and separating the fraction C to obtain aniline and benzothiazole. The method disclosed by the invention is capable of realizing the resourceful treatment of the 2-mercaptobenzothiazole production waste and has the advantages of various by-products, good product quality, simpleness in process flow, easiness in operation, mildness in reaction condition, low production cost and is environment-friendly.

Description

A kind of treatment process of 2-mercaptobenzothiazole processing waste
Technical field
The present invention relates to Chemical Manufacture waste disposal technical field, be specifically related to a kind of treatment process of 2-mercaptobenzothiazole processing waste.
Background technology
2-mercaptobenzothiazole is a captax, is the important vulcanization accelerator of rubber industry, is again the fertile material and the midbody of other most of promotor, can the multiple promotor of output after further synthesizing processing.2-mercaptobenzothiazole output accounts for the first place in various rubber ingredients, all there is the output of hundreds of thousands of ton every year in the whole world, and domestic conservative calculating also will have 200,000 tons output in 2012.
The working method commonly used of captax is a high-pressure process; With dithiocarbonic anhydride, sulphur, aniline is raw material; Earlier dithiocarbonic anhydride and sulphur are processed molten sulphur liquid by 3: 1 mixed; Dissolve sulphur liquid afterwards and drop in the autoclave by 1: 1 ratio with aniline again and heat, when temperature reaches 280-290 ℃, maintenance made captax half a hour when pressure reached 3.0-9.5Mpa.The high-pressure process reaction product is complicated mixture, is main with captax wherein, and the content of captax is 77-85%, also has unreacted raw material, intermediate product and by product etc. in addition, the general designation spent resin, and its content is 15-23%.The reaction product that high-pressure process makes also must be about to captax and separate with spent resin through further refining purification, makes the satisfactory captax of purity.At present the process for purification of captax mainly contains two kinds of acid-base method and extracted in toluene methods.Refining back is except that the product captax that obtains, and remaining waste material is the 2-mercaptobenzothiazole processing waste of indication of the present invention.Wherein the staple of the refining residue waste material that obtains of acid-base method and approximately content be: M content >=5%, aniline content is about 2.4%, benzothiazole >=22%, a small amount of hydrogen sulfide, all the other are the complicated impurity that is difficult to characterize.The staple of the refining residue waste material that obtains of extracted in toluene method and about content thereof: M content≤25%, aniline content is about 1.8%, benzothiazole>=18%, toluene level 2.2-2.8%, a small amount of hydrogen sulfide, all the other are the complicated impurity that is difficult to characterize.The captax that to produce 200,000 tons in 2012 by domestic conservative estimation calculates, and will produce 4.6 ten thousand tons 2-mercaptobenzothiazole processing waste.
Staple M in the 2-mercaptobenzothiazole processing waste, toluene, aniline, benzothiazole etc., these residues mostly can not natural degradations, and dangerous; It is useless in the environmental protection register, to be classified as danger; A large amount of M waste residues were both dangerous, and contaminate environment becomes an environmental protection difficult problem again.Handle the 2-mercaptobenzothiazole processing waste at present following method is arranged: one, directly as end shelves waterproof roll or concrete mold separant; Its shortcoming is that objectionable constituent do not obtain handling; The user uses the back objectionable impurities can long-term diffusion, contaminate environment, is detrimental to health; Two, as burning in boiler kerosene or blast furnace joint filling material, this treatment process is directly to burn in fact, and atmosphere has been caused pollution again.The most important thing is that above two kinds of treatment processs all are the utilizations to the simple and low value of 2-mercaptobenzothiazole processing waste, thus cause the price of present 2-mercaptobenzothiazole processing waste not high always, 1200 yuan/ton only of historic highs.Therefore, developing a kind of recycling processing method of 2-mercaptobenzothiazole processing waste, to increase value-added content of product, increase economic efficiency, effectively reduce environmental pollution, is a difficult problem being badly in need of solution at present.
Summary of the invention
The object of the present invention is to provide a kind of treatment process of 2-mercaptobenzothiazole processing waste.
In order to realize above purpose, the technical scheme that the present invention adopted is: a kind of treatment process of 2-mercaptobenzothiazole processing waste may further comprise the steps:
(1) solid-liquid separation: the 2-mercaptobenzothiazole processing waste is heated to 90~95 ℃, puts into whizzer afterwards and carry out solid-liquid separation, obtain solid substance and liquid A, said solid substance returns the captax workshop and makes with extra care purification, obtains the product captax;
(2) liquid distillation: carry out fractionation by distillation in the still kettle with said liquid A adding distillation tower, vacuum tightness is more than the 0.07Mpa in the control distillation tower; The tower top temperature of distillation tower is 60~115 ℃, and the gained fraction collection is fraction B; The tower top temperature of distillation tower is 115~190 ℃, collects the gained cut, gets cut C; Tower top temperature begins to reduce and does not have when cut flows out and stops to distill; Open drain hole and emit residue in the still kettle, said residue gets bituminous substances D through cooling; The stink damp body and function sodium hydroxide solution that in the fractionation by distillation process, produces absorbs, and makes sodium hydrosulfide, obtains the Sodium sulfhydrate solid through concentrating again;
(3) rectification process: said cut C is the miscellany of aniline and benzothiazole, carries out rectifying separation in the rectifying still with said cut C adding rectifying tower, and vacuum tightness is more than the 0.07Mpa in the control rectifying tower; The tower top temperature of rectifying tower is 175~180 ℃, and the gained fraction collection obtains aniline, and the tower top temperature of rectifying tower is 180~190 ℃, and the gained fraction collection obtains benzothiazole, and tower top temperature begins reduction and do not have to stop rectifying when cut flows out.
The fraction B that the treatment process of 2-mercaptobenzothiazole processing waste provided by the invention obtains is the mixture or the water of toluene and water; When the 2-mercaptobenzothiazole processing waste is the refining residue waste material that obtains of acid-base method; Fraction B is a water; When the 2-mercaptobenzothiazole processing waste was made with extra care the residue waste material that obtains for the extracted in toluene method, fraction B was the mixture of toluene and water.When fraction B was the mixture of toluene and water, fraction B was through leaving standstill, and natural layering separablely goes out toluene.The bituminous substances D softening temperature that obtains is more than 220 ℃; Objectionable constituent wherein and residual M are carbonized; Its chemical property is stable; For black has no irritating odor and environment is not had the general waste material of harm, can be used by production of resins enterprise as a kind of modified resin, oil fuel can also be extracted and also good economic benefits can be produced.The purity of the aniline that obtains is greater than 99.5%, and the purity of benzothiazole is greater than 98%, but direct marketing.
The treatment process of 2-mercaptobenzothiazole processing waste provided by the invention has the following advantages: one, the environmental protection contribution is big; Through the various poisonous and harmfuls in the 2-mercaptobenzothiazole processing waste, volatile material are extracted; Make the 2-mercaptobenzothiazole processing waste no longer produce harm, fundamentally solved the environmental pollution difficult problem of 2-mercaptobenzothiazole processing waste environment; And in the entire treatment process, do not have waste water, waste gas to produce, avoided secondary environmental pollution; Two, economize on resources, about about 45% the material in the 2-mercaptobenzothiazole processing waste has all become useful product, has practiced thrift the resources of production greatly; Three, good in economic efficiency; Added value of product is high; After adopting the disposal methods of 2-mercaptobenzothiazole processing waste provided by the invention, the output value of 2-mercaptobenzothiazole processing waste is extended to original more than six times, the product captax, toluene, aniline, benzothiazole, the Sodium sulfhydrate that obtain; All be important chemical material, economic worth is high.
The present invention has realized the recycling treatment of 2-mercaptobenzothiazole processing waste; And it is many to have the sub product kind; Good product quality, technical process is simple, facility investment is few, easy handling, reaction conditions gentle, production cost is low and advantage such as compliance with environmental protection requirements.The present invention has good economic benefit, environmental benefit and social benefit, is fit to industrial production and promotes, and has broad application prospects.
Embodiment
Embodiment 1
The treatment process of the 2-mercaptobenzothiazole processing waste that present embodiment provides, 2-mercaptobenzothiazole processing waste wherein are the refining residue waste material that obtains of acid-base method, may further comprise the steps:
(1) solid-liquid separation: the 2-mercaptobenzothiazole processing waste of getting 200kg; With being steam heated to 90 ℃, put into whizzer afterwards and carry out solid-liquid separation, obtain the liquid A of solid substance 64kg and 126kg; Solid substance returns the captax workshop and makes with extra care purification, obtains the product captax of 40kg;
(2) liquid distillation: liquid A is added in the still kettle of distillation tower and carry out fractionation by distillation, vacuum tightness is 0.07Mpa in the control distillation tower; The tower top temperature of distillation tower is 60~115 ℃, and the gained cut is a water, and the tower top temperature of distillation tower is 115~190 ℃; Collect the gained cut, get cut C, altogether 49.6kg; Be the miscellany of aniline and benzothiazole, tower top temperature begins to reduce and does not have when cut flows out and stops to distill, and opens drain hole and emits residue in the still kettle; Residue gets bituminous substances D through cooling; The stink damp body and function sodium hydroxide solution that in the fractionation by distillation process, produces absorbs, and makes sodium hydrosulfide, obtains Sodium sulfhydrate solid 10.8kg through concentrating again;
(3) rectification process: carry out rectifying separation in the rectifying still with cut C adding rectifying tower, vacuum tightness is 0.07Mpa in the control rectifying tower; The tower top temperature of rectifying tower is 175~180 ℃, and the gained fraction collection obtains aniline, and the tower top temperature of rectifying tower is 180~190 ℃, and the gained fraction collection obtains benzothiazole, and tower top temperature begins reduction and do not have to stop rectifying when cut flows out.The heavy 4.8kg of the aniline that obtains, purity is 99.5%.The heavy 44kg of the benzothiazole that obtains, purity is 99%.
Embodiment 2
The treatment process of the 2-mercaptobenzothiazole processing waste that present embodiment provides, 2-mercaptobenzothiazole processing waste wherein is the refining residue waste material that obtains of extracted in toluene method, may further comprise the steps:
(1) solid-liquid separation: the 2-mercaptobenzothiazole processing waste of getting 200kg; With being steam heated to 95 ℃, put into whizzer afterwards and carry out solid-liquid separation, obtain the liquid A of solid substance 65kg and 125kg; Solid substance returns the captax workshop and makes with extra care purification, obtains the product captax of 42kg;
(2) liquid distillation: liquid A is added in the still kettle of distillation tower and carry out fractionation by distillation, vacuum tightness is 0.07Mpa in the control distillation tower; The tower top temperature of distillation tower is 60~115 ℃, and the gained fraction collection gets fraction B, altogether 10kg; Be the mixture of toluene and water, the tower top temperature of distillation tower is 115~190 ℃, collects the gained cut, gets cut C; 40kg is the miscellany of aniline and benzothiazole altogether, and tower top temperature begins to reduce and do not have when cut flows out and stops to distill; Open drain hole and emit residue in the still kettle, residue gets bituminous substances D through cooling; The stink damp body and function sodium hydroxide solution that in the fractionation by distillation process, produces absorbs, and makes sodium hydrosulfide, obtains Sodium sulfhydrate solid 11kg through concentrating again;
(3) rectification process: carry out rectifying separation in the rectifying still with cut C adding rectifying tower, vacuum tightness is 0.07Mpa in the control rectifying tower; The tower top temperature of rectifying tower is 175~180 ℃, and the gained fraction collection obtains aniline, and the tower top temperature of rectifying tower is 180~190 ℃, and the gained fraction collection obtains benzothiazole, and tower top temperature begins reduction and do not have to stop rectifying when cut flows out.The heavy 3.6kg of the aniline that obtains, purity is 99.6%.The heavy 36.4kg of the benzothiazole that obtains, purity is 98.6%.Fraction B in the step (2) is therefrom isolated toluene through standing demix, gets toluene 5kg.

Claims (3)

1. the treatment process of a 2-mercaptobenzothiazole processing waste is characterized in that, may further comprise the steps:
(1) solid-liquid separation: the 2-mercaptobenzothiazole processing waste is heated to 90~95 ℃, puts into whizzer afterwards and carry out solid-liquid separation, obtain solid substance and liquid A, said solid substance returns the captax workshop and makes with extra care purification, obtains the product captax;
(2) liquid distillation: carry out fractionation by distillation in the still kettle with said liquid A adding distillation tower, vacuum tightness is more than the 0.07Mpa in the control distillation tower; The tower top temperature of distillation tower is 60~115 ℃, and the gained fraction collection is fraction B; The tower top temperature of distillation tower is 115~190 ℃, collects the gained cut, gets cut C; Tower top temperature begins to reduce and does not have when cut flows out and stops to distill; Open drain hole and emit residue in the still kettle, said residue gets bituminous substances D through cooling; The stink damp body and function sodium hydroxide solution that in the fractionation by distillation process, produces absorbs, and makes sodium hydrosulfide, obtains the Sodium sulfhydrate solid through concentrating again;
(3) rectification process: said cut C is the miscellany of aniline and benzothiazole, carries out rectifying separation in the rectifying still with said cut C adding rectifying tower, and vacuum tightness is more than the 0.07Mpa in the control rectifying tower; The tower top temperature of rectifying tower is 175~180 ℃, and the gained fraction collection obtains aniline, and the tower top temperature of rectifying tower is 180~190 ℃, and the gained fraction collection obtains benzothiazole, and tower top temperature begins reduction and do not have to stop rectifying when cut flows out.
2. the treatment process of 2-mercaptobenzothiazole processing waste according to claim 1 is characterized in that, the purity of the aniline that obtains is greater than 99.5%.
3. the treatment process of 2-mercaptobenzothiazole processing waste according to claim 1 is characterized in that, the purity of the benzothiazole that obtains is greater than 98%.
CN2012100399188A 2012-02-21 2012-02-21 Method for treating 2-mercaptobenzothiazole production waste Active CN102603668B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2012100399188A CN102603668B (en) 2012-02-21 2012-02-21 Method for treating 2-mercaptobenzothiazole production waste

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2012100399188A CN102603668B (en) 2012-02-21 2012-02-21 Method for treating 2-mercaptobenzothiazole production waste

Publications (2)

Publication Number Publication Date
CN102603668A true CN102603668A (en) 2012-07-25
CN102603668B CN102603668B (en) 2013-11-27

Family

ID=46521505

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2012100399188A Active CN102603668B (en) 2012-02-21 2012-02-21 Method for treating 2-mercaptobenzothiazole production waste

Country Status (1)

Country Link
CN (1) CN102603668B (en)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106243059A (en) * 2016-07-26 2016-12-21 濮阳蔚林化工股份有限公司 A kind of method extracting benzothiazole from 2 benzothiazolyl mercaptans production by-products
CN106518803A (en) * 2016-10-08 2017-03-22 扬中市橡胶塑料厂有限公司 Rubber vulcanization accelerator for high-abrasion-resistance rubber sealing piece production
CN106967007A (en) * 2017-03-06 2017-07-21 山东尚舜化工有限公司 A kind of processing method of rubber accelerator M resins
CN107286910A (en) * 2017-06-29 2017-10-24 可名芸 A kind of harmless treatment process of spent resin
CN107721947A (en) * 2017-12-05 2018-02-23 河南恒瑞橡塑科技股份有限公司 A kind of green clean synthesis process for producing benzothiazole
CN109111410A (en) * 2018-10-11 2019-01-01 科迈化工股份有限公司 A kind of processing method of acid-base method 2-mercaptobenzothiazole production waste material
CN109535099A (en) * 2018-10-24 2019-03-29 科迈化工股份有限公司 Method by recycling MBT in resin
CN109608417A (en) * 2018-10-24 2019-04-12 科迈化工股份有限公司 Method by recycling the direct synthesis accelerant MBTS of crude product MBT in resin
CN112919469A (en) * 2021-01-28 2021-06-08 河南乾瑞化工科技有限公司 Recycling method of waste resin of accelerator M
CN113461638A (en) * 2020-03-30 2021-10-01 中石化南京化工研究院有限公司 Recycling method of accelerator M tar
CN114805241A (en) * 2022-06-24 2022-07-29 山东戴瑞克新材料有限公司 Benzothiazole and preparation method thereof
CN115403539A (en) * 2022-08-11 2022-11-29 山东戴瑞克新材料有限公司 M resin stripping method containing aniline and benzothiazole

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4780540A (en) * 1986-02-14 1988-10-25 Bayer Aktiengesellschaft Process for working up tars containing 2-mercaptobenzothiazole
CN101215271A (en) * 2008-01-16 2008-07-09 天津市科迈化工有限公司 Method of separating rubber vulcanization accelerator MBT
CN101245052A (en) * 2008-03-14 2008-08-20 何连峰 Method for extracting benzothiazole with by-product for producing 2-mercaptobenzothiazole
CN101402615A (en) * 2008-11-12 2009-04-08 山东阳谷华泰化工有限公司 Fine purification method for rubber vulcanization accelerant 2-mercaptobenzothiazole (M)
CN101693701A (en) * 2009-10-21 2010-04-14 山东阳谷华泰化工股份有限公司 Purification process for vulcanization accelerator 2-mercaptobenzothiazole

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4780540A (en) * 1986-02-14 1988-10-25 Bayer Aktiengesellschaft Process for working up tars containing 2-mercaptobenzothiazole
CN101215271A (en) * 2008-01-16 2008-07-09 天津市科迈化工有限公司 Method of separating rubber vulcanization accelerator MBT
CN101245052A (en) * 2008-03-14 2008-08-20 何连峰 Method for extracting benzothiazole with by-product for producing 2-mercaptobenzothiazole
CN101402615A (en) * 2008-11-12 2009-04-08 山东阳谷华泰化工有限公司 Fine purification method for rubber vulcanization accelerant 2-mercaptobenzothiazole (M)
CN101693701A (en) * 2009-10-21 2010-04-14 山东阳谷华泰化工股份有限公司 Purification process for vulcanization accelerator 2-mercaptobenzothiazole

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106243059A (en) * 2016-07-26 2016-12-21 濮阳蔚林化工股份有限公司 A kind of method extracting benzothiazole from 2 benzothiazolyl mercaptans production by-products
CN106518803A (en) * 2016-10-08 2017-03-22 扬中市橡胶塑料厂有限公司 Rubber vulcanization accelerator for high-abrasion-resistance rubber sealing piece production
CN106967007A (en) * 2017-03-06 2017-07-21 山东尚舜化工有限公司 A kind of processing method of rubber accelerator M resins
CN107286910A (en) * 2017-06-29 2017-10-24 可名芸 A kind of harmless treatment process of spent resin
CN107721947A (en) * 2017-12-05 2018-02-23 河南恒瑞橡塑科技股份有限公司 A kind of green clean synthesis process for producing benzothiazole
CN109111410A (en) * 2018-10-11 2019-01-01 科迈化工股份有限公司 A kind of processing method of acid-base method 2-mercaptobenzothiazole production waste material
CN109111410B (en) * 2018-10-11 2022-05-03 科迈化工股份有限公司 Treatment method of waste material produced by acid-base method 2-mercaptobenzothiazole
CN109608417B (en) * 2018-10-24 2023-04-07 科迈化工股份有限公司 Method for directly synthesizing accelerator MBTS by recovering crude MBT from resin
CN109535099A (en) * 2018-10-24 2019-03-29 科迈化工股份有限公司 Method by recycling MBT in resin
CN109608417A (en) * 2018-10-24 2019-04-12 科迈化工股份有限公司 Method by recycling the direct synthesis accelerant MBTS of crude product MBT in resin
CN113461638A (en) * 2020-03-30 2021-10-01 中石化南京化工研究院有限公司 Recycling method of accelerator M tar
CN113461638B (en) * 2020-03-30 2023-10-13 中石化南京化工研究院有限公司 Recycling method of accelerator M tar
CN112919469A (en) * 2021-01-28 2021-06-08 河南乾瑞化工科技有限公司 Recycling method of waste resin of accelerator M
CN114805241B (en) * 2022-06-24 2023-08-18 山东戴瑞克新材料有限公司 Benzothiazole and preparation method thereof
CN114805241A (en) * 2022-06-24 2022-07-29 山东戴瑞克新材料有限公司 Benzothiazole and preparation method thereof
CN115403539A (en) * 2022-08-11 2022-11-29 山东戴瑞克新材料有限公司 M resin stripping method containing aniline and benzothiazole

Also Published As

Publication number Publication date
CN102603668B (en) 2013-11-27

Similar Documents

Publication Publication Date Title
CN102603668B (en) Method for treating 2-mercaptobenzothiazole production waste
CN100447187C (en) Process of reclaimed rubber by improved high-temperature dynamic desulfurization
CN105237394A (en) Preparation method of diisobutyl phthalate
CN103012090B (en) Method for recovering organic matters in polyester wastewater
CN108017109B (en) Method for recycling BDO waste liquid
CN105016346A (en) Green method for comprehensively utilizing biomass ash
CN207552149U (en) A kind of oil sludge handles recycling system
CN201313874Y (en) Waste acrylic acid and acrylic ester recovery device
CN104479721A (en) Fuel oil preparation technique utilizing waste plastics
CN105175242A (en) Method for recycling trichlorotoluene and/or benzoyl chloride waste slag
CN104214784A (en) Medical waste treatment method
CN102485801A (en) Preparation method of biological tar waterproof paste
CN108395362A (en) A method of extracting biphenyl using heat carrier heating negative pressure rectifying
CN104211658B (en) The production method of new type rubber sulphur accelerant MBT
CN103450249B (en) The process for purification of methyl cyclosiloxane
CN106675672B (en) A kind of high-flash coal tar alcohol-based fuel and preparation method thereof
CN203648118U (en) Resource utilization equipment aiming at dimethyl formamide (DMF) rectification residues
CN104673351A (en) Cracking process of waste rubber
CN211546372U (en) Production system for recycling butyl acrylate heavy components
CN103059586A (en) Preparation method of waterproof cream from biological tar
CN219050365U (en) PVC system high-boiling-point material recycling device
CN203095981U (en) Solid waste carbonization device
CN210384893U (en) Recovery device for steam condensate
CN102923895A (en) Method for disposing cyclohexanone saponified waste liquid
CN203648119U (en) Equipment for deeply recovering DMF (Dimethyl Formamide) solvent for DMF rectifying residues

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
TR01 Transfer of patent right

Effective date of registration: 20220629

Address after: 458000 jijiashan Industrial Park, Heshan District, Hebi City, Henan Province

Patentee after: HEBI HENGLI RUBBER CO.,LTD.

Address before: 456250 No. 276, Gongren lane, Jiefang Road, Daokou Town, Hua county, Hebi City, Henan Province

Patentee before: Liu Zhao

TR01 Transfer of patent right