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

CN103709833B - Preparation method for polymer coated inorganic pigment paste for color modulation of production line - Google Patents

Preparation method for polymer coated inorganic pigment paste for color modulation of production line Download PDF

Info

Publication number
CN103709833B
CN103709833B CN201310711210.7A CN201310711210A CN103709833B CN 103709833 B CN103709833 B CN 103709833B CN 201310711210 A CN201310711210 A CN 201310711210A CN 103709833 B CN103709833 B CN 103709833B
Authority
CN
China
Prior art keywords
inorganic pigment
production line
polymer overmold
mineral dye
color paste
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.)
Active
Application number
CN201310711210.7A
Other languages
Chinese (zh)
Other versions
CN103709833A (en
Inventor
吕仕铭
杜长森
周华
梅成国
付少海
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.)
Changshu Famous Chemical Technology Co., Ltd.
Original Assignee
SUZHOU SHIMING TECHNOLOGY 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 SUZHOU SHIMING TECHNOLOGY Co Ltd filed Critical SUZHOU SHIMING TECHNOLOGY Co Ltd
Priority to CN201310711210.7A priority Critical patent/CN103709833B/en
Publication of CN103709833A publication Critical patent/CN103709833A/en
Application granted granted Critical
Publication of CN103709833B publication Critical patent/CN103709833B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

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

Abstract

The invention relates to a polymer coated inorganic pigment paste for color modulation of a production line and a preparation method thereof. The polymer coated inorganic pigment paste for color modulation of the production line comprises the following components by mass percent: 40-60% of polymer coated inorganic pigment concentrated paste including 40-60% of inorganic pigment by mass, 0.5-2% of surface tension modifier, 10-30% of water soluble organic solvent, 0.1-0.5% of defoamer, 0.01-0.05% of antibacterial agent, and the balance of water. The polymer coated inorganic pigment paste for color modulation of the production line provided by the invention has the advantages such as small grain size, good tinting strength and high storage stability; besides, the paste can be stored for a long time without generating obvious chromatic aberration; therefore, the polymer coated inorganic pigment paste is especially applied as a water-based color paste to color modulation of the production line.

Description

The production line toning preparation method of polymer overmold inorganic pigment color paste
Technical field
The present invention relates to technical field of fine, be specifically related to a kind of production line toning polymer overmold inorganic pigment color paste and preparation method thereof.
Background technology
Coating production line toning integral system is a kind of novel tinting system, and it is by toning software control colour mixer, and mill base is directly injected barreled coating by cubing mode, then through capping, concussion, realizes coating automatic color regulating.Mineral dye has sun-proof, heat-resisting, weathering resistance, solvent resistance are good, the feature of strong covering power for cobalt blue, ferric oxide, carbon black etc., is the pigment variety of coating industry large usage quantity, is also the main inorganic colorant material of coating production line toning integral system.Because the grain diameter of mineral dye and density are large, dispersing auxiliary is not easily adsorbed in surface, easily there is the phenomenons such as granules of pigments particle diameter becomes large, sedimentation in the aqueous color paste that therefore mineral dye is made, cause tinting strength significantly to reduce in storage process.And once mill base tinting strength reduces, then colour mixer must be caused to mix colours and occur deviation, cause client returns, even coating is scrapped.
The rigors that inorganic pigment color paste prepared by general technology there will not be sedimentation after being difficult to meet production line toning use mill base long-time storage, tinting strength reduces, therefore, the inorganic pigment color paste that Preparation and storage stability is high be production line mix colours integrated tinting material produce gordian technique.In recent years, more about the research preparing production line toning nano dye mill base, but the Basic practice preparing mill base is all attrition process under dispersion agent is assisted.Such as, publication number is that the Chinese patent of CN1986660 discloses the method with high polymer dispersant being prepared by mineral dye dispersion to water-base inorganic pigment color paste; Publication number is that the Chinese patent of CN101760085 discloses the method adopting dispersion agent directly to be prepared by mineral dye processing to inner-outer wall emulsion paint toning inorganic pigment color paste; The patent No. is the method that the United States Patent (USP) of US6489393 and US7268180 then discloses the pigment such as titanium white, mica and prepares mill base, the pigment component that it adopts except containing except oxide compound, not through other modification.But the phenomenon such as pigment sedimentation, tinting strength reduction that dispersion agent desorption causes often can occur mill base prepared by these techniques in long-time storage process, be difficult to use in production line toning.
Dispersion agent is adopted directly to disperse mineral dye, there is dispersion agent little at surface of pigments adsorption, the defects such as desorption phenomenon is serious, after long-time storage, very easily because pigment agglomerates, pigment particles particle diameter becomes and causes greatly degradation problem under the tinting strength of inorganic pigment color paste in mill base, and when dispersant concentration is higher, dispersion viscosity can be caused excessive, easy to foaming, so also can reduce production line toning accuracy and circulation ratio, cause produce coating occur batch difference.
Summary of the invention
In view of this, the present invention aims to provide high production line toning polymer overmold inorganic pigment color paste of a kind of stability in storage and preparation method thereof, this production line toning polymer overmold inorganic pigment color paste can meet coating production line toning integral system and colour mixer to the storage of mill base used and retention of color requirement.
In order to realize object of the present invention, one aspect of the present invention provides a kind of production line toning polymer overmold inorganic pigment color paste, and it comprises following component by mass percentage:
Polymer overmold mineral dye thickened pulp 40-60%, in described polymer overmold mineral dye thickened pulp, the quality accounting of mineral dye is 40-60%;
Surface tension modifier 0.5-2%;
Water-miscible organic solvent 10-30%;
Defoamer 0.1-0.5%;
Antiseptic-germicide 0.01-0.05%;
Surplus is water.
Preferably, described mineral dye is the one in carbon black, cobalt blue or ferric oxide.
Preferably, described water-miscible organic solvent comprises at least one in n-propyl alcohol, propyl carbinol, ethylene glycol, propylene glycol, BDO, 1,6-hexylene glycol, glycol ether, Triethylene glycol, tetraethylene-glycol, glycerol.
Preferably, described surface tension modifier is aniorfic surfactant or nonionic surface active agent, or it is composite and obtain by both, and described aniorfic surfactant is the one in sodium lauryl sulphate, Sodium dodecylbenzene sulfonate, potassium oleate, sodium alkyl naphthalene sulfonate, sodium abietate, described nonionic surface active agent is the one of polyoxyethylene alkylphenol condenses, polyoxyethylene fatty alcohol condenses, polyoxyethylene polyols ether fatty acid ester, polyoxyethylene fatty acid ester class tensio-active agent.
Preferably, described defoamer is the one in polyethers, polysiloxane-based, organic silicon modified by polyether class.
The present invention provides the preparation method of the production line toning polymer overmold inorganic pigment color paste described in a kind of above-described embodiment on the other hand, and it comprises the steps:
A) be that the mineral dye of 40-80% is distributed in low boiling point solvent by accounting for low boiling point solvent mass ratio, add successively and account for silane coupling agent that mineral dye mass ratio is 5-15%, account for the deionized water that silane coupling agent mass ratio is 50-100%, react while stirring, obtain starting inorganic pigment slurry;
B) add in described starting inorganic pigment slurry and account for the polymkeric substance that mineral dye massfraction is 10-40%, on sand mill after grinding distribution, add and account for the deionized water that low boiling point solvent mass ratio is 80-200%, again pH value is adjusted to 8-9, mix, after filtration, obtain polymer overmold mineral dye slurry;
C) carry out underpressure distillation to described polymer overmold mineral dye slurry, remove low boiling point solvent and part water, the quality accounting obtaining mineral dye is the polymer overmold mineral dye thickened pulp of 40-60%;
D) in described polymer overmold mineral dye thickened pulp, described surface tension modifier, water-miscible organic solvent, defoamer, antiseptic-germicide and water is added by the mass percent of each component in described production line toning polymer overmold inorganic pigment color paste, stir, obtain described production line toning polymer overmold inorganic pigment color paste.
Preferably, described silane coupling agent comprises γ-aminopropyl triethoxysilane, 3-(2,3-epoxy third oxygen) propyl trimethoxy silicane, γ-methacryloxypropyl trimethoxy silane, gamma-mercaptopropyltriethoxysilane, γ-mercaptopropyl trimethoxysilane, N-β-aminoethyl-γ-aminopropyltriethoxy dimethoxysilane and N-(β-aminoethyl) at least one in-γ-aminopropyltrimethoxysilane.
Preferably, described low boiling point solvent comprise in methyl alcohol, ethanol, Virahol, hexanaphthene, diisopropyl ether, acetone, butanone one or both.
Preferably, described polymkeric substance is the polymkeric substance containing carboxyl or anhydride functional group in molecular chain.
Preferably, described polymkeric substance is the one in styrene-acrylic resins, phenylethylene-maleic anhydride resin, maleic-acrylic acid ester copolymer, vinylbenzene-itaconic acid copolymer.
The production line toning polymer overmold inorganic pigment color paste that the embodiment of the present invention provides has that particle diameter is little, tinting strength and stability in storage advantages of higher, and this mill base can prolonged storage and do not produce obvious aberration.This production line toning polymer overmold inorganic pigment color paste can meet coating production line toning integral system and colour mixer to the storage of mill base used and retention of color requirement, is particularly suitable for as production line toning use mill base.
Embodiment
In order to make object of the present invention, technical scheme and advantage clearly understand, below in conjunction with embodiment, the present invention is further elaborated.Should be appreciated that specific embodiment described herein only in order to explain the present invention, be not intended to limit the present invention.
The embodiment of the present invention provides a kind of production line toning polymer overmold inorganic pigment color paste on the one hand, and it comprises following component by mass percentage:
Polymer overmold mineral dye thickened pulp 40-60%, in this polymer overmold mineral dye thickened pulp, the quality accounting of mineral dye is 40-60%;
Surface tension modifier 0.5-2%;
Water-miscible organic solvent 10-30%;
Defoamer 0.1-0.5%;
Antiseptic-germicide 0.01-0.05%;
Surplus is water.
In a preferred embodiment, mineral dye is the one in carbon black, cobalt blue or ferric oxide.Mineral dye has sun-proof, heat-resisting, weathering resistance, solvent resistance are good, the feature of strong covering power for cobalt blue, ferric oxide, carbon black etc.
In a preferred embodiment, water-miscible organic solvent comprises at least one in n-propyl alcohol, propyl carbinol, ethylene glycol, propylene glycol, BDO, 1,6-hexylene glycol, glycol ether, Triethylene glycol, tetraethylene-glycol, glycerol.These water-miscible organic solvents, by the character of its high boiling point, low melting point, effectively can promote moisturizing and the freeze-thaw stability of production line toning polymer overmold inorganic pigment color paste.
In a preferred embodiment, surface tension modifier is aniorfic surfactant or nonionic surface active agent, or it is composite and obtain by both, and aniorfic surfactant is the one in sodium lauryl sulphate, Sodium dodecylbenzene sulfonate, potassium oleate, sodium alkyl naphthalene sulfonate, sodium abietate, nonionic surface active agent is the one of polyoxyethylene alkylphenol condenses, polyoxyethylene fatty alcohol condenses, polyoxyethylene polyols ether fatty acid ester, polyoxyethylene fatty acid ester class tensio-active agent.Specifically, the commercial nonionic surface active agent product that the present invention can select has: trade name is the polyoxyethylene alkylphenol condenses of OP-7, OP-10 or OP-15, trade name is the polyoxyethylene fatty alcohol condenses of paregal O-10, paregal O-20, peregal O-25 or peregal A-20, trade name is the polyoxyethylene polyols ether fatty acid ester of Tween40, Tween60, Tween65, Tween80, and trade name is the polyoxyethylene fatty acid ester of SG-10, SE-10, OE-15.
In a preferred embodiment, defoamer is the one in polyethers, polysiloxane-based, organic silicon modified by polyether class.
It should be noted that, as long as can ensure that mill base can be applied in the production line toning polymer overmold inorganic pigment color paste that embodiment in the present invention provides storing and there will not be the mouldy or smelly phenomenon because bacteria breed causes in use procedure and meet the antiseptic-germicide that coating industry relevant laws and regulations limit.The preferred organic antibacterial agent of antiseptic-germicide used or natural antibacterial agent, the organic antibacterial agent that can select has the antiseptic-germicides such as vanilla aldehydes, ethyl vanillin aldehydes, anilid class, imidazoles, thiazoles, isothiazolone derivative, quaternary ammonium salt, biguanides and phenols; Natural antibacterial agent then can select chitin, mustard, Viscotrol C and horseradish.
The present invention also provides a kind of preparation method of above-mentioned production line toning polymer overmold inorganic pigment color paste, and it comprises the steps:
A) be that the mineral dye of 40-80% is distributed in low boiling point solvent by accounting for low boiling point solvent mass ratio, add successively and account for silane coupling agent that mineral dye mass ratio is 5-15%, account for the deionized water that silane coupling agent mass ratio is 50-100%, react while stirring, obtain starting inorganic pigment slurry;
B) add in starting inorganic pigment slurry and account for the polymkeric substance that mineral dye massfraction is 10-40%, on sand mill after grinding distribution, add and account for the deionized water that low boiling point solvent mass ratio is 80-200%, again pH value is adjusted to 8-9, mix, after filtration, obtain polymer overmold mineral dye slurry;
C) carry out underpressure distillation to polymer overmold mineral dye slurry, remove low boiling point solvent and part water, the quality accounting obtaining mineral dye is the polymer overmold mineral dye thickened pulp of 40-60%;
D) in polymer overmold mineral dye thickened pulp, surface tension modifier, water-miscible organic solvent, defoamer, antiseptic-germicide and water is added by the mass percent of each component in above-mentioned production line toning polymer overmold inorganic pigment color paste, stir, obtain production line toning polymer overmold inorganic pigment color paste.
Particularly, in step a), stirring velocity is 500-1000r/min, and the reaction times is 6-24 hour.In step b), grinding distribution 3-10 time on sand mill, then the pH value adding pH value regulator adjustment mineral dye slurry is 8-9.In the inside of sand mill, can effectively be reduced the pigment particle size in pigment slurry by the high shear force that the grinding medium of high degree of agitation provides and make pigment with more small particle size distribution in the slurry.Usually, a process of lapping is difficult to reach satisfied grinding effect, often needs slurry by sand mill grinding distribution 3-10 time.PH value regulator can be the one in sodium hydroxide, potassium hydroxide, ammoniacal liquor and trolamine.In step c), general control temperature is at 30-60 DEG C, and pressure is at 0.02-0.08Mpa.In step d), surface tension modifier, water-miscible organic solvent, defoamer, antiseptic-germicide and water can be added successively in polymer overmold mineral dye thickened pulp, be uniformly mixed, and after 100-300 order filter-cloth filtering, namely obtain this production line toning polymer overmold inorganic pigment color paste.
In a preferred embodiment, silane coupling agent comprises γ-aminopropyl triethoxysilane, 3-(2,3-epoxy third oxygen) propyl trimethoxy silicane, γ-methacryloxypropyl trimethoxy silane, gamma-mercaptopropyltriethoxysilane, γ-mercaptopropyl trimethoxysilane, N-β-aminoethyl-γ-aminopropyltriethoxy dimethoxysilane and N-(β-aminoethyl) at least one in-γ-aminopropyltrimethoxysilane.Particularly, silane coupling agent general formula can be: Y (CH 2) nsiX 3.In formula, n=0-3(n is integer); X is hydrolysable group, is generally alkoxyl group, as methoxyl group, oxyethyl group, methoxy ethoxy, acetoxyl group, methacryloxypropyl etc.; Y is organo-functional group, as amino, vinyl epoxy base, methacryloxy, mercapto propyl group etc.More specifically, the present invention can select at least one in the silane coupling agents such as KH-550, KH-560, KH-570, KH-580, KH-590, KH-602, the KH-792 named according to Chinese Academy of Sciences's coupling agent naming system.Because silane coupling agent can play a role well at the temperature of 0-40 DEG C, therefore, step a) can operate at nominal room temperature, does not need extra measure of heating.
Low boiling point solvent used can be organic solvent, and its target selected is that selected low boiling point solvent can remove to greatest extent in the underpressure distillation of step c) from polymer overmold mineral dye thickened pulp.In a preferred embodiment, low boiling point solvent comprises one or both in methyl alcohol, ethanol, Virahol, hexanaphthene, diisopropyl ether, acetone, butanone.
The polymkeric substance used in step b) must have good solubility energy in selected low boiling point solvent, and solvability in water is poor.In a preferred embodiment, polymkeric substance is the polymkeric substance containing carboxyl or anhydride functional group in molecular chain.Further preferably, polymkeric substance is the one in styrene-acrylic resins, phenylethylene-maleic anhydride resin, maleic-acrylic acid ester copolymer, vinylbenzene-itaconic acid copolymer.
The production line toning polymer overmold inorganic pigment color paste that the embodiment of the present invention provides has that particle diameter is little, tinting strength and stability in storage advantages of higher, and this mill base can prolonged storage and do not produce obvious aberration.This production line toning polymer overmold inorganic pigment color paste can meet coating production line toning integral system and colour mixer to the storage of mill base used and retention of color requirement, is particularly suitable for as production line toning use mill base.
The advantage embodying the production line toning polymer overmold inorganic pigment color paste that the embodiment of the present invention provides will be compared below by several embodiment and comparative example.
Embodiment 1:
65 grams of carbon black dispersion are in 160 grams of acetone, then 4.5 grams of silane resin acceptor kh-550s are dripped successively, 5 grams of KH-602 and 5 gram deionized waters, under room temperature, low whipping speed is react 6 hours under 500r/min, add 6.5 grams of styrene-acrylic resins again, on use for laboratory miniature sand mill after grinding distribution 3 times, add 128 grams of deionized waters, add a certain amount of trolamine again, stir, the pH value of system is made to be 8, after mixing, acetone again under 30 DEG C and 0.02MPa pressure in underpressure distillation removal system and part water, styrene-acrylic resins is deposited to be coated on the surface of charcoal blacks, final obtained 130 grams of polymer overmold charcoal blacks thickened pulp.
3 grams of sodium lauryl sulphate, 20 grams of glycerol and 10 grams of ethylene glycol, 0.15 gram of polysiloxane defoamer, 0.015 gram of isothiazolone derivative class antiseptic-germicide and 56.9 grams of deionized waters are added successively in 60 grams of polymer overmold charcoal blacks thickened pulp, be uniformly mixed, obtained polymer overmold charcoal blacks mill base.
Embodiment 2:
50 grams of ferric oxide red colorants are distributed in 100 grams of ethanol, then 5 grams of Silane coupling reagent KH-570s and 4 grams of deionized waters are dripped successively, low whipping speed is react 24 hours under 800r/min, add 5 grams of vinylbenzene-itaconic acid copolymers again, stir, on use for laboratory miniature sand mill after grinding distribution 10 times, add 200 grams of deionized waters and the appropriate 30%NaOH aqueous solution, make system ph value is 8, after mixing, ethanol again under 40 DEG C and 0.08MPa pressure in underpressure distillation removal system and part water, make vinylbenzene-itaconic acid copolymer deposit and be coated on the surface of ferric oxide red colorant, obtained 77 grams of polymer overmold ferric oxide red colorant thickened pulp.
2 grams of Tween80,10 grams of tetraethylene-glycols, 10 grams of ethylene glycol and 10 grams of propylene glycol, 0.3 gram of polyethers defoamer, 0.03 gram of vanilla aldehydes antiseptic-germicide and 28 grams of deionized waters are added successively in 40 grams of waterborne polymeric coated iron oxide red thickened pulp, be uniformly mixed, obtained polymer overmold ferric oxide red colorant mill base.
Embodiment 3:
60 grams of cobalt blue dyes are distributed in 75 grams of methyl alcohol, then 3 grams of silane coupling agent KH-560 and 3 gram deionized waters are dripped successively, low whipping speed is react 24 hours under 1000r/min, add 24 grams of phenylethylene-maleic anhydride resins again, on use for laboratory miniature sand mill after grinding distribution 6 times, add 150 grams of deionized waters and a certain amount of 30%KOH aqueous solution, stir, the pH value of system is made to be 9, methyl alcohol again under 60 DEG C and 0.06MPa pressure in underpressure distillation removal system and part water, phenylethylene-maleic anhydride pitch deposition is made to be coated on the surface of cobalt blue dye, obtained 120 grams of polymer overmold cobalt blue dye thickened pulp.
0.5 gram of OP-15,10 grams of propylene glycol, 0.5 gram of organic silicon modified by polyether defoamer, 0.05 gram of imidazoles antiseptic-germicide and 29 grams of deionized waters are added successively in 60 grams of polymer overmold cobalt blue dye thickened pulp, be uniformly mixed, obtained polymer overmold cobalt blue dye mill base.
Embodiment 4:
42 grams of carbon black dispersion are in the mixed solution of 40 grams of hexanaphthenes and 20 grams of Virahols, then 2.5 grams of silane coupling agent KH-792 and 2 gram deionized waters are dripped successively, low whipping speed is react 18 hours under 500r/min, add 10 grams of maleic-acrylic acid ester resins again on use for laboratory miniature sand mill after grinding distribution 8 times, add the ammonia soln of 100 grams of deionized waters and appropriate 17%, stir, the pH value of system is made to be 8, hexanaphthene under 30 DEG C and 0.06MPa pressure in underpressure distillation removal system and part water, maleic-acrylic acid ester pitch deposition is made to be coated on the surface of charcoal blacks, obtained polymer overmold charcoal blacks thickened pulp.
1 gram of paregal O-20,20 grams of ethylene glycol, 0.3 gram of polysiloxane defoamer, 0.03 gram of chitin antibacterial agent and 28.67 grams of deionized waters are added successively in 50 grams of polymer overmold charcoal blacks thickened pulp, be uniformly mixed, obtained polymer overmold charcoal blacks mill base.
Comparative example 5:
65 grams of carbon black dispersion are in 160 grams of acetone, add 6.5 grams of styrene-acrylic resins, on use for laboratory miniature sand mill after grinding distribution 3 times, add 128 grams of deionized waters, add a certain amount of trolamine again, stir, the pH value of system is made to be 8, after mixing, acetone again under 30 DEG C and 0.02MPa pressure in underpressure distillation removal system and part water, styrene-acrylic resins is deposited to be coated on the surface of charcoal blacks, final obtained 130 grams of polymer overmold charcoal blacks thickened pulp.
3 grams of sodium lauryl sulphate, 20 grams of glycerol and 10 grams of ethylene glycol, 0.15 gram of polysiloxane defoamer, 0.015 gram of isothiazolone derivative class antiseptic-germicide and 56.9 grams of deionized waters are added successively in 60 grams of polymer overmold charcoal blacks thickened pulp, be uniformly mixed, obtained production line toning polymer overmold charcoal blacks mill base.
Comparative example 6
65 grams of carbon black dispersion are in 160 grams of acetone, then 4.5 grams of silane resin acceptor kh-550s, 5 grams of KH-602 and 5 gram deionized waters are dripped successively, under room temperature, low whipping speed is react 6 hours under 500r/min, solvent under 30 DEG C and 0.02MPa pressure in underpressure distillation removal system and water, 60 DEG C after 12 hours, obtain the carbon black powder after surface treatment with drying under 0.02MPa pressure.
After 160 grams of water, 6.5 grams of styrene-acrylic resins and a certain amount of trolamine are mixed, obtain the mixed solution that pH value is 8, carbon black powder after surface treatment is dropped into after this mixed solution disperses 6 hours, this mixed solution of grinding distribution 3 times on use for laboratory miniature sand mill again, and the part water under 30 DEG C and 0.02MPa pressure in underpressure distillation removal system, final obtained 130 grams of polymer overmold charcoal blacks thickened pulp.
3 grams of sodium lauryl sulphate, 20 grams of glycerol and 10 grams of ethylene glycol, 0.15 gram of polysiloxane defoamer, 0.015 gram of isothiazolone derivative class antiseptic-germicide and 56.9 grams of deionized waters are added successively in 60 grams of polymer overmold charcoal blacks thickened pulp, be uniformly mixed, obtained production line toning polymer overmold charcoal blacks mill base.
Performance test:
Mill base prepared by B method (instrumental method) the testing example 1-4 described by HG/T3951-2007 Appendix B and comparative example 5,6 is in the relative color strength change that just preparation is complete and normal temperature storage is after 180 days, embodiment 1-4 store at 25 DEG C the mill base after 180 days respectively with the mill base before the storage of correspondence for standard mill base, namely just prepare complete mill base tinting strength with embodiment 1-4 and be respectively 100%, all just prepare complete mill base tinting strength for 100% with embodiment 1 before and after comparative example 5,6 normal temperature storage, test the relative color strength change of its normal temperature storage after 180 days.Simultaneously, aqueous color paste airtight placement of difference at 25 DEG C prepared by embodiment 1-4 and comparative example 5,6, after 180 days, has a strong impact on the situation of stability to judge the stability in storage of aqueous color paste by visual observations with or without appearance obvious granules of pigments precipitation, flocculation etc.Size distribution before and after airtight placement 180 days at the aqueous color paste 25 DEG C prepared with the Zetasizer Nano Zs90 type nano particle size of Malvern Instr Ltd. of Britain and zeta potential instrument testing example 1-4 and comparative example 5,6, in test result, D50 represents and represents median size with D50 by the minimum grain size that the particle of in surveyed particle 50% can pass through.Each sample test 3 times, if median size differs and is no more than 10% at every turn, then get the mean value of 3 times as median size, if median size differs by more than 10%, then retest 3 times, the median size of again testing differs at every turn and is no more than 10%, then get and again test the mean value of 3 times as median size, otherwise indicates " cannot Measurement accuracy ".
The result that the aqueous color paste that table 1 is prepared for Application Example 1-4 is tested according to aforesaid method.Wherein in stability in storage test, " √ " represents that range estimation is without exception, and "×" represents that the situations such as obvious granules of pigments precipitation, flocculation appear in range estimation.
Table 1. embodiment 1-4 and comparative example 5,6 prepare mill base test result
Can be found out by the test result of embodiment and comparative example, the production line toning polymer overmold inorganic pigment color paste that the embodiment of the present invention provides has high, the particle diameter of storage stability and the less feature of tinting strength change, compared to comparative example 5 and use tradition dispersion, comparative example 6 prepared by Ginding process has a clear superiority in.
The foregoing is only preferred embodiment of the present invention, not in order to limit the present invention, all any amendments done within the spirit and principles in the present invention, equivalent replacement and improvement etc., all should be included within protection scope of the present invention.

Claims (6)

1. a production line is mixed colours by the preparation method of polymer overmold inorganic pigment color paste, described production line toning polymer overmold inorganic pigment color paste by mass percentage, comprise following component: polymer overmold mineral dye thickened pulp 40-60%, in described polymer overmold mineral dye thickened pulp, the quality accounting of mineral dye is 40-60%; Surface tension modifier 0.5-2%; Water-miscible organic solvent 10-30%; Defoamer 0.1-0.5%; Antiseptic-germicide 0.01-0.05%; Surplus is water; It is characterized in that, described preparation method comprises the steps:
A) be that the mineral dye of 40-80% is distributed in low boiling point solvent by accounting for low boiling point solvent mass ratio, add successively and account for silane coupling agent that mineral dye mass ratio is 5-15%, account for the deionized water that silane coupling agent mass ratio is 50-100%, react while stirring, obtain starting inorganic pigment slurry;
B) add in described starting inorganic pigment slurry and account for the polymkeric substance that mineral dye massfraction is 10-40%, on sand mill after grinding distribution, add and account for the deionized water that low boiling point solvent mass ratio is 80-200%, again pH value is adjusted to 8-9, mix, after filtration, obtain polymer overmold mineral dye slurry;
C) carry out underpressure distillation to described polymer overmold mineral dye slurry, remove low boiling point solvent and part water, the quality accounting obtaining mineral dye is the polymer overmold mineral dye thickened pulp of 40-60%;
D) in described polymer overmold mineral dye thickened pulp, described surface tension modifier, water-miscible organic solvent, defoamer, antiseptic-germicide and water is added by the mass percent of each component in described production line toning polymer overmold inorganic pigment color paste, stir, obtain described production line toning polymer overmold inorganic pigment color paste;
Described silane coupling agent comprises at least one in γ-aminopropyl triethoxysilane, 3-(2,3-epoxy third oxygen) propyl trimethoxy silicane, γ-methacryloxypropyl trimethoxy silane, gamma-mercaptopropyltriethoxysilane, γ-mercaptopropyl trimethoxysilane, N-β-aminoethyl-γ-aminopropyltriethoxy dimethoxysilane and N-(β-aminoethyl)-γ-aminopropyltrimethoxysilane;
Described polymkeric substance is the polymkeric substance containing carboxyl or anhydride functional group in molecular chain, and described polymkeric substance is the one in styrene-acrylic resins, phenylethylene-maleic anhydride resin, maleic-acrylic acid ester copolymer, vinylbenzene-itaconic acid copolymer.
2. the preparation method of production line toning polymer overmold inorganic pigment color paste according to claim 1, it is characterized in that, described low boiling point solvent comprise in methyl alcohol, ethanol, Virahol, hexanaphthene, diisopropyl ether, acetone, butanone one or both.
3. the preparation method of production line toning polymer overmold inorganic pigment color paste according to claim 1, it is characterized in that, described mineral dye is the one in carbon black, cobalt blue or ferric oxide.
4. the preparation method of production line toning polymer overmold inorganic pigment color paste according to claim 1, it is characterized in that, described water-miscible organic solvent comprises n-propyl alcohol, propyl carbinol, ethylene glycol, propylene glycol, 1, at least one in 4-butyleneglycol, 1,6-hexylene glycol, glycol ether, Triethylene glycol, tetraethylene-glycol, glycerol.
5. the preparation method of production line toning polymer overmold inorganic pigment color paste according to claim 1, it is characterized in that, described surface tension modifier is aniorfic surfactant or nonionic surface active agent, or it is composite and obtain by both, and described aniorfic surfactant is sodium lauryl sulphate, Sodium dodecylbenzene sulfonate, potassium oleate, sodium alkyl naphthalene sulfonate, one in sodium abietate, described nonionic surface active agent is polyoxyethylene alkylphenol condenses, polyoxyethylene fatty alcohol condenses, polyoxyethylene polyols ether fatty acid ester, the one of polyoxyethylene fatty acid ester class tensio-active agent.
6. the preparation method of production line toning polymer overmold inorganic pigment color paste according to claim 1, is characterized in that, described defoamer is the one in polyethers, polysiloxane-based, organic silicon modified by polyether class.
CN201310711210.7A 2013-12-20 2013-12-20 Preparation method for polymer coated inorganic pigment paste for color modulation of production line Active CN103709833B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201310711210.7A CN103709833B (en) 2013-12-20 2013-12-20 Preparation method for polymer coated inorganic pigment paste for color modulation of production line

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201310711210.7A CN103709833B (en) 2013-12-20 2013-12-20 Preparation method for polymer coated inorganic pigment paste for color modulation of production line

Publications (2)

Publication Number Publication Date
CN103709833A CN103709833A (en) 2014-04-09
CN103709833B true CN103709833B (en) 2015-04-01

Family

ID=50403203

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201310711210.7A Active CN103709833B (en) 2013-12-20 2013-12-20 Preparation method for polymer coated inorganic pigment paste for color modulation of production line

Country Status (1)

Country Link
CN (1) CN103709833B (en)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105273493B (en) * 2015-02-11 2018-03-06 上海荟百精细化工有限公司 Excellent gravure pearl ink of a kind of storage characteristics and preparation method thereof
CN107629484A (en) * 2017-09-20 2018-01-26 包头市中科投资管理有限公司 A kind of pigment preparations and preparation method thereof
CN109054463B (en) * 2018-08-06 2021-01-26 浙江锦达膜材科技有限公司 Preparation method of high-dispersibility pigment for PVC (polyvinyl chloride) film structural material
CN109021685B (en) * 2018-09-21 2022-03-22 汕头市光彩新材料科技有限公司 Hydrophobic color fixing ink and preparation process thereof
CN109535774A (en) * 2018-11-19 2019-03-29 岳西县邦玉铁系颜料有限公司 A kind of high temperature resistant mica-iron oxide pigment
US20200325341A1 (en) * 2019-04-12 2020-10-15 Viavi Solutions Inc. Method for manufacturing a special effect pigment
CN110437502B (en) * 2019-08-13 2020-10-27 北京化工大学 Preparation method of polymer-coated particles
CN110835471B (en) * 2019-11-19 2021-06-18 广州市汇合彩颜料有限公司 Preparation method of low-volatility organic solvent for grinding pigment
CN111040458A (en) * 2019-12-30 2020-04-21 司徒志成 Universal modified rosin liquid color masterbatch composition and its preparation method and use
CN113913051A (en) * 2020-07-10 2022-01-11 立邦涂料(中国)有限公司 High-concentration stable water-based environment-friendly ferric oxide color paste for color mixer and preparation method thereof
CN112608080B (en) * 2020-12-08 2023-02-03 广东省福美材料科学技术有限公司 Color active mixed material and preparation method and application thereof
CN113278307A (en) * 2021-04-30 2021-08-20 江苏可奥熙光学材料科技有限公司 Preparation method of strong oxidation resistant pigment for optical lens resin
CN117659770A (en) * 2022-08-22 2024-03-08 立邦涂料(中国)有限公司 Environment-friendly water-based high-concentration inorganic pigment color paste and preparation method and application thereof
CN115505289B (en) * 2022-11-04 2023-03-24 佛山市彩贵新型材料有限公司 Black ceramic ink, preparation method and application thereof, and ceramic product

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6585818B2 (en) * 2001-07-27 2003-07-01 Lexmark International, Inc. Pigment ink formulation
JP4303086B2 (en) * 2003-10-28 2009-07-29 東芝テック株式会社 Pigment dispersion, UV curable ink jet ink precursor, ink jet recording method, printed matter, and method for producing pigment dispersion
JP5055022B2 (en) * 2007-05-24 2012-10-24 理想科学工業株式会社 Water-based ink for inkjet
US20110197782A1 (en) * 2010-02-18 2011-08-18 Silberline Manufacturing Company, Inc. Gold colored metallic pigments that include manganese oxide nanoparticles
US8912252B2 (en) * 2010-07-20 2014-12-16 Silberline Manufacturing Company, Inc. Film-forming pigments and coating system including the same

Also Published As

Publication number Publication date
CN103709833A (en) 2014-04-09

Similar Documents

Publication Publication Date Title
CN103709833B (en) Preparation method for polymer coated inorganic pigment paste for color modulation of production line
CN102372949B (en) Aqueous pigment slurry and preparation method thereof
US12116486B2 (en) Coated pigment
CN101679795B (en) Aqueous pigment preparations comprising anionic additives based on allyl ether and vinyl ether
JP3948934B2 (en) Aluminum pigment, method for producing the same, and resin composition
CN101654589B (en) Water-based bi-component polyurethane color paint
CN101613553B (en) Dope for plastic decorative cover of automotive wheel and preparation method thereof
CN108034305B (en) Ferric oxide pigment color paste and preparation method thereof
CN104194562B (en) A kind of normal temperature cure monocomponent nanocomposite composite aqueous paint preparation method
JP5201401B2 (en) Infrared reflective black pigment, paint and resin composition using the infrared reflective black pigment
CN105255261B (en) A kind of aqueous color paste and preparation method thereof
CN106366882B (en) A kind of flexible self polishing copolymer antifouling paint and preparation method thereof with anti-drag function
CN110511633A (en) A kind of aqueous marine antifouling coating of low VOC content
CN107674528B (en) High-performance multicolor paint and preparation method thereof
CN104559590A (en) Exterior wall paint used in high-temperature, high-humidity and strong ultraviolet region and production method thereof
CN102676012A (en) Pure acrylic outer wall emulsion paint
CN105111813A (en) Preparation method of polyurethane modified acrylate polymeric dispersant for coatings
CN101659814B (en) Preparation method of water-borne polyurethane color paste
CN101735718A (en) Method for preparing self-drying dilutable alkyd paint
CN105670485B (en) A kind of nanometer of Al2O3Modified polyurethane resin coating and preparation method thereof
CN108864811A (en) A kind of two-way mirror ink and preparation method thereof that weatherability is good
CN106675211A (en) Water-based high-gloss anti-rust carbon black color paste, as well as preparation method and application thereof
CN102304311B (en) Aqueous aluminum paste composition and preparation method thereof
CN107974154A (en) A kind of preparation method of modified water-soluble nano paint
CN109401420A (en) Additive capable of generating pearlescent effect and preparation method thereof

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
C41 Transfer of patent application or patent right or utility model
TR01 Transfer of patent right

Effective date of registration: 20170124

Address after: 215500 Haining Road, Changshu new material industrial park, Jiangsu, China, No. 12, No.

Patentee after: Changshu Famous Chemical Technology Co., Ltd.

Address before: 215337 Kunshan, Jiangsu, Huangpu River Road, No. 219, North Road, No.

Patentee before: Suzhou Shiming Technology Co., Ltd.