CN102304298A - Pigment red 254 postprocessing technology - Google Patents

Pigment red 254 postprocessing technology Download PDF

Info

Publication number
CN102304298A
CN102304298A CN201110167976A CN201110167976A CN102304298A CN 102304298 A CN102304298 A CN 102304298A CN 201110167976 A CN201110167976 A CN 201110167976A CN 201110167976 A CN201110167976 A CN 201110167976A CN 102304298 A CN102304298 A CN 102304298A
Authority
CN
China
Prior art keywords
pigment red
weight
crude product
solution
paratonere
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
CN201110167976A
Other languages
Chinese (zh)
Inventor
何勇恒
赵觉新
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.)
Nantong Municipal Zhengyan Pigment Chemicals Co Ltd
Original Assignee
Nantong Municipal Zhengyan Pigment Chemicals 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 Nantong Municipal Zhengyan Pigment Chemicals Co Ltd filed Critical Nantong Municipal Zhengyan Pigment Chemicals Co Ltd
Priority to CN201110167976A priority Critical patent/CN102304298A/en
Publication of CN102304298A publication Critical patent/CN102304298A/en
Pending legal-status Critical Current

Links

Landscapes

  • Pigments, Carbon Blacks, Or Wood Stains (AREA)

Abstract

The invention discloses a pigment red 254 postprocessing technology, which is characterized by comprising the following steps of: adding a crude product of pigment red 254 into a reaction kettle, and adding 95 mass percent organic solution and 30 mass percent NaOH solution, wherein the weight of the added organic solution is 9 to 11 times that of the crude product of pigment red 254, and the weight of the added NaOH solution is 0.05 to 0.1 time that of the crude product of pigment red 254; heating to the temperature of between 60 and 80DEG C, stirring for 4.5 to 5.5 hours; pressing the materials into a filter press, washing the materials with more than 95 mass percent organic solvent of which the weight is 1.5 to 3 times that of the pigment red 254, washing with water until the pH value of filtrate is 8; and drying the obtained filter cake with the solid content of 40-45 percent in a common oven to obtain the finished product. The invention has the advantages that: the pigment red 254 postprocessing technology is easy and convenient to operate, the work efficiency is high and the produced product has higher stability.

Description

The aftertreatment technology of Pigment red 254
Technical field
The present invention relates to the aftertreatment technology of Pigment red 254, belong to chemical field.
Background technology
Aftertreatment technology to Pigment red 254 generally is to adopt grinding technics at present, and this process energy consumption is higher, and production capacity is very low, and loss ratio is bigger.
Summary of the invention
The objective of the invention is: to above-mentioned deficiency, the aftertreatment technology of a kind of processing ease, simple, energy consumption is low, efficient is high Pigment red 254 is provided.
For realizing above-mentioned purpose, the technical scheme that the present invention adopts is:
The aftertreatment technology of paratonere 254; It is characterized in that: comprise the steps; Crude product with paratonere 254 adds in the reactor at normal temperatures; Add mass concentration simultaneously and be 95% organic solution and mass concentration and be 30% NaOH solution; The weight of the organic solution that adds is 9-11 times of paratonere 254 crude product weight; The weight of the NaOH solution that adds is 0.05-0.1 times of paratonere 254 crude product weight; Rising temperature to 60-80 ℃; And stirred 4.5-5.5 hours; Then material is pressed in the filter press; Material is washed greater than 95% organic solvent with mass concentration; The weight of the organic solvent that adds is 1.5-3 times of paratonere 254 weight; After organic solvent uses; Then use water washing again; PH value until filtrating is 8, is that 40%-45% filter cake is put into a conventional oven and carried out drying with the solid content of gained, gets product.
Further, described NaOH solution can replace with deionized water, and the weight of deionized water is 1.5-2.5 times of Pigment red 254 crude product weight.
Further, said organic solution is any one in methanol solution, ethanolic soln or the DMF solution.
Further, said organic solvent is any one among methyl alcohol, ethanol or the DMF.
Advantage of the present invention is: the aftertreatment technology of Pigment red 254 of the present invention, and than adopting grinding technics that Pigment red is carried out aftertreatment, its operation is more convenient, simple, and working efficiency is higher, and the product stability of making is better.
Embodiment
Below all embodiment further specify of the present invention, but do not limit protection scope of the present invention.
Embodiment 1
The crude product of the Pigment red 254 of 300 weight parts is added in the reaction kettle; Add 2900 weight part concentration simultaneously and be 95% methanol solution and 20 weight part concentration and be 30% NaOH solution; Elevated temperature to 65 ℃; And stirred 4.5 hours; Then material is pressed in the pressure filter; With the mass concentration of 500 weight parts greater than 95% methanol wash; After organic solvent uses; Use water washing again; PH value up to filtrating is 8; Be that 40% filter cake is put a conventional oven into and carried out drying then with 700 weight part solid contents, get product.
Embodiment 2
The crude product of the Pigment red 254 of 300 weight parts is added in the reaction kettle; Add 3200 weight part concentration simultaneously and be 95% ethanolic soln and 20 weight part concentration and be 30% NaOH solution; Elevated temperature to 75 ℃; And stirred 5 hours; Then material is pressed in the pressure filter; With the mass concentration of 500 weight parts greater than 95% methanol wash; After organic solvent uses; Use water washing again; PH value up to filtrating is 8; Be that 42% filter cake is put a conventional oven into and carried out drying then with 700 weight part solid contents, get product.
Embodiment 3
The crude product of the Pigment red 254 of 300 weight parts is added in the reaction kettle; Then, adding 2950 weight part concentration simultaneously is the deionized water of DMF solution and 500 weight parts, and elevated temperature is to reflux temperature; And stirred 4 hours; Then material is pressed in the pressure filter, with 800 weight part mass concentrations greater than 95% DMF washing, after organic solvent uses; Use water washing again; PH value up to filtrating is 8, is that 45% filter cake is put a conventional oven into and carried out drying then with 700 weight part solid contents, gets product.
The aftertreatment technology of Pigment red 254 of the present invention, than adopting grinding technics that Pigment red is carried out aftertreatment, its operation is more convenient, simple, and working efficiency is higher, and the product stability of making is better.

Claims (4)

1. the aftertreatment technology of paratonere 254; It is characterized in that: comprise the steps; Crude product with paratonere 254 adds in the reactor at normal temperatures; Add mass concentration simultaneously and be 95% organic solution and mass concentration and be 30% NaOH solution; The weight of the organic solution that adds is 9-11 times of paratonere 254 crude product weight; The weight of the NaOH solution that adds is 0.05-0.1 times of paratonere 254 crude product weight; Rising temperature to 60-80 ℃; And stirred 4.5-5.5 hours; Then material is pressed in the filter press; Material is washed greater than 95% organic solvent with mass concentration; The weight of the organic solvent that adds is 1.5-3 times of paratonere 254 weight; After organic solvent uses; Then use water washing again; PH value until filtrating is 8, is that 40%-45% filter cake is put into a conventional oven and carried out drying with the solid content of gained, gets product.
2. the aftertreatment technology of Pigment red 254 according to claim 1 is characterized in that: described NaOH solution can replace with deionized water, and the weight of deionized water is 1.5-2.5 times of Pigment red 254 crude product weight.
3. the aftertreatment technology of Pigment red 254 according to claim 1 is characterized in that: said organic solution is any one in methanol solution, ethanolic soln or the DMF solution.
4. the aftertreatment technology of Pigment red 254 according to claim 1 is characterized in that: said organic solvent is any one among methyl alcohol, ethanol or the DMF.
CN201110167976A 2011-06-22 2011-06-22 Pigment red 254 postprocessing technology Pending CN102304298A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201110167976A CN102304298A (en) 2011-06-22 2011-06-22 Pigment red 254 postprocessing technology

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201110167976A CN102304298A (en) 2011-06-22 2011-06-22 Pigment red 254 postprocessing technology

Publications (1)

Publication Number Publication Date
CN102304298A true CN102304298A (en) 2012-01-04

Family

ID=45378221

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201110167976A Pending CN102304298A (en) 2011-06-22 2011-06-22 Pigment red 254 postprocessing technology

Country Status (1)

Country Link
CN (1) CN102304298A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104403349A (en) * 2014-11-29 2015-03-11 嘉兴科隆化工有限公司 Industrial production method of pigment yellow 97
CN108250789A (en) * 2018-02-08 2018-07-06 浙江浩川科技有限公司 A kind of preparation method of paratonere 254

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101555362A (en) * 2008-04-11 2009-10-14 富士胶片株式会社 Pigment dispersing composition and manufacturing method thereof, coloured polymerized composition, colour filter and manufacturing method thereof
CN101624476A (en) * 2009-08-10 2010-01-13 南通市争妍颜料化工有限公司 Production process of pigment red HT
CN101831197A (en) * 2010-05-17 2010-09-15 南通市争妍颜料化工有限公司 Production process for pigment red 254 variety HL with high covering power
CN101896257A (en) * 2007-12-10 2010-11-24 巴斯夫欧洲公司 Production of a solid pigment preparation in the form of granules by spray drying

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101896257A (en) * 2007-12-10 2010-11-24 巴斯夫欧洲公司 Production of a solid pigment preparation in the form of granules by spray drying
CN101555362A (en) * 2008-04-11 2009-10-14 富士胶片株式会社 Pigment dispersing composition and manufacturing method thereof, coloured polymerized composition, colour filter and manufacturing method thereof
CN101624476A (en) * 2009-08-10 2010-01-13 南通市争妍颜料化工有限公司 Production process of pigment red HT
CN101831197A (en) * 2010-05-17 2010-09-15 南通市争妍颜料化工有限公司 Production process for pigment red 254 variety HL with high covering power

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104403349A (en) * 2014-11-29 2015-03-11 嘉兴科隆化工有限公司 Industrial production method of pigment yellow 97
CN104403349B (en) * 2014-11-29 2017-07-21 嘉兴科隆化工有限公司 A kind of industrialized preparing process of pigment yellow 97
CN108250789A (en) * 2018-02-08 2018-07-06 浙江浩川科技有限公司 A kind of preparation method of paratonere 254

Similar Documents

Publication Publication Date Title
CN102603000B (en) Process for preparing high-purity vanadium pentoxide by adopting ammonium metavanadate as raw material
CN103333075A (en) Production method of 2,5-dichloroaniline
CN102304298A (en) Pigment red 254 postprocessing technology
CN105417616B (en) The method that organic wastewater is handled with industrial residue manganese dioxide
CN102190298A (en) Method for preparing active carbon from carbon byproduct in fast pyrolysis of forest remainder
CN102240554A (en) Pollution-free preparation process for catalyst used in preparation of formaldehyde through methanol oxidation by iron-molybdenum method
CN103834395A (en) Method for preparing luminescent carbon dots from glycerin
CN103319307A (en) Method for preparing sodium soap
CN103769211B (en) A kind of preparation method of the hybrid inorganic-organic materials supported ruthenium catalyst for the synthesis of L-aminopropanol
CN106000436A (en) Preparation method of heterogeneous catalyst with camphor tree ash as carrier and application thereof
CN103073031A (en) Method for preparing lithium fluoride from phosphate fertilizer by-product sodium fluoride
CN101597250A (en) Acid copper intermediate sodium polydithio-dipropyl sulfonate synthetic method
CN104592040A (en) Preparation method of rubber antioxidant p-phenylenediamine
CN101423224A (en) Potassium borofluoride preparation method based on fluosilicic acid and boron rock
CN102659572B (en) Preparation method of dehydroabietic acid
CN202705337U (en) Device for producing fatty acid by utilizing swill-cooked dirty oil
CN101723925A (en) Preparation method of 7-hydroxy-4-methylcoumarin
CN101475168B (en) Method for washing active carbon
CN102351699A (en) Gulonate and preparation method thereof
CN106045864A (en) Production process for preparing 4-chloro-2,5-dimethoxyaniline with hydrazine hydrate catalytic reduction method
CN103265728B (en) Preparation method of cobalt decanoate adhesion promoter with high performance and low cobalt content
CN105503789A (en) Method for catalytic conversion of xylose into furfural by use of montmorillonite-supported metal ion solid acid
CN106986389A (en) A kind of method that utilization graphite oxide production process Waste Sulfuric Acid prepares manganese sulfate
CN103113234B (en) Method for synthesizing N-methyl paranitroaniline
CN102824920A (en) Method for preparing furfural solid-acid catalyst through utilizing corn stalks

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication

Application publication date: 20120104

RJ01 Rejection of invention patent application after publication