CN106833190B - Dedicated sealing wax of polypropylene plastics and preparation method thereof - Google Patents
Dedicated sealing wax of polypropylene plastics and preparation method thereof Download PDFInfo
- Publication number
- CN106833190B CN106833190B CN201710018483.1A CN201710018483A CN106833190B CN 106833190 B CN106833190 B CN 106833190B CN 201710018483 A CN201710018483 A CN 201710018483A CN 106833190 B CN106833190 B CN 106833190B
- Authority
- CN
- China
- Prior art keywords
- agent
- sealing wax
- polypropylene plastics
- parts
- dedicated sealing
- 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
Links
- 239000012173 sealing wax Substances 0.000 title claims abstract description 63
- 239000004743 Polypropylene Substances 0.000 title claims abstract description 54
- 239000004033 plastic Substances 0.000 title claims abstract description 52
- 229920003023 plastic Polymers 0.000 title claims abstract description 52
- -1 polypropylene Polymers 0.000 title claims abstract description 50
- 229920001155 polypropylene Polymers 0.000 title claims abstract description 49
- 238000002360 preparation method Methods 0.000 title claims abstract description 10
- 239000002270 dispersing agent Substances 0.000 claims abstract description 35
- 239000000203 mixture Substances 0.000 claims abstract description 34
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 24
- 239000000049 pigment Substances 0.000 claims abstract description 22
- 239000002562 thickening agent Substances 0.000 claims abstract description 18
- 239000011347 resin Substances 0.000 claims abstract description 17
- 229920005989 resin Polymers 0.000 claims abstract description 17
- 239000000853 adhesive Substances 0.000 claims abstract description 16
- 230000001070 adhesive effect Effects 0.000 claims abstract description 16
- 239000006184 cosolvent Substances 0.000 claims abstract description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000002518 antifoaming agent Substances 0.000 claims abstract description 13
- 239000000080 wetting agent Substances 0.000 claims abstract description 12
- 239000003002 pH adjusting agent Substances 0.000 claims abstract description 9
- 239000002318 adhesion promoter Substances 0.000 claims abstract description 7
- 239000008367 deionised water Substances 0.000 claims abstract description 5
- 229910021641 deionized water Inorganic materials 0.000 claims abstract description 5
- 239000003973 paint Substances 0.000 claims description 31
- 239000007788 liquid Substances 0.000 claims description 12
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 10
- 230000009477 glass transition Effects 0.000 claims description 10
- 238000002156 mixing Methods 0.000 claims description 10
- 229910052710 silicon Inorganic materials 0.000 claims description 10
- 239000010703 silicon Substances 0.000 claims description 10
- 238000003756 stirring Methods 0.000 claims description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 9
- 150000001412 amines Chemical class 0.000 claims description 9
- 239000011265 semifinished product Substances 0.000 claims description 8
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical group O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 7
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 5
- 238000001914 filtration Methods 0.000 claims description 5
- 229920000570 polyether Polymers 0.000 claims description 5
- 238000004537 pulping Methods 0.000 claims description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical class OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 4
- 239000004925 Acrylic resin Substances 0.000 claims description 4
- 229920000178 Acrylic resin Polymers 0.000 claims description 4
- 239000004814 polyurethane Substances 0.000 claims description 4
- 239000002994 raw material Substances 0.000 claims description 4
- 239000000377 silicon dioxide Substances 0.000 claims description 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 3
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 claims description 3
- 239000000908 ammonium hydroxide Substances 0.000 claims description 3
- 229960002887 deanol Drugs 0.000 claims description 3
- 239000012972 dimethylethanolamine Substances 0.000 claims description 3
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 claims description 2
- 229920001400 block copolymer Polymers 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical group CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 2
- 229920002635 polyurethane Polymers 0.000 claims description 2
- 239000004408 titanium dioxide Substances 0.000 claims description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims 1
- 125000003158 alcohol group Chemical group 0.000 claims 1
- 238000001035 drying Methods 0.000 abstract description 14
- 239000011342 resin composition Substances 0.000 abstract description 2
- 238000000576 coating method Methods 0.000 description 22
- 239000011248 coating agent Substances 0.000 description 20
- CUDYYMUUJHLCGZ-UHFFFAOYSA-N 2-(2-methoxypropoxy)propan-1-ol Chemical group COC(C)COC(C)CO CUDYYMUUJHLCGZ-UHFFFAOYSA-N 0.000 description 9
- 239000000126 substance Substances 0.000 description 8
- CUVLMZNMSPJDON-UHFFFAOYSA-N 1-(1-butoxypropan-2-yloxy)propan-2-ol Chemical compound CCCCOCC(C)OCC(C)O CUVLMZNMSPJDON-UHFFFAOYSA-N 0.000 description 7
- 239000000945 filler Substances 0.000 description 6
- 238000003860 storage Methods 0.000 description 5
- 229910014314 BYK190 Inorganic materials 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 235000010215 titanium dioxide Nutrition 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 239000003643 water by type Substances 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 239000013530 defoamer Substances 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000007665 sagging Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 229920006351 engineering plastic Polymers 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 238000007306 functionalization reaction Methods 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000002068 microbial inoculum Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 239000006223 plastic coating Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000012462 polypropylene substrate Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 230000037452 priming Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/0427—Coating with only one layer of a composition containing a polymer binder
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C09D167/08—Polyesters modified with higher fatty oils or their acids, or with natural resins or resin acids
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
- C09D7/62—Additives non-macromolecular inorganic modified by treatment with other compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/65—Additives macromolecular
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/10—Homopolymers or copolymers of propene
- C08J2323/12—Polypropene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2433/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2467/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
- C08J2467/08—Polyesters modified with higher fatty oils or their acids, or with resins or resin acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
- C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Paints Or Removers (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Sealing Material Composition (AREA)
Abstract
The present invention provides dedicated sealing wax of a kind of polypropylene plastics and preparation method thereof, the composition of the second resin composition of the first resin and 25-40 weight % that the film forming matter of the dedicated sealing wax of polypropylene plastics is 60-75 weight %.The dedicated sealing wax of polypropylene plastics of the present invention further includes having adhesion promoter, pH adjusting agent, deionized water, cosolvent, dispersing agent, defoaming agent, pigment, anti-settling agent, wetting agent, levelling agent, thickener as needed.Not only adhesive force is strong for the dedicated sealing wax of polypropylene plastics, and drying time is short, and has very high hardness and lower VOC content, easy to use and to the basic nonhazardous of human body.
Description
Technical field
The present invention relates to water paint fields, and in particular to a kind of dedicated sealing wax of polypropylene plastics and preparation method thereof.
Background technique
With the promotion of people's living standard and the continuous development of plastics industry, plastics have become must in people's daily life
Indispensable a part.Polypropylene is general-purpose plastics with the fastest developing speed after polyvinyl chloride, polyethylene, big logical as three
With plastics, yield is increasing, and especially in recent years, people mould polypropylene by versatility polyacrylic crystalline modified research
Expect to rapidly develop to functional plastic and engineering plastics, realizes the functionalization and high performance of general-purpose plastics, widely answered
For industries such as automobile, pipelines.Since polarity of polypropylene is small or nonpolarity, and have the characteristics that crystallinity, surface are smooth, thus it is difficult
To form adhesive force well between paint film and plastic bottom material.
The existing method for solving paint film and polypropylene plastics adhesion problem and measure have following several: can be to its table
The special processing that comes to the surface, such as the oxidation of corona (spark processing) chromic acid, plasma discharge are taken in face, but these processing exist
Very big disadvantage is unfavorable for environmental requirement first is that polluting the environment, and in addition processing cost is also higher, therefore is actually using
On be very limited.And positive solution is to develop a kind of pair of plastic components surface with good adhesive force
Coating.
PP substrate coatings are substantially oiliness PP paint at present, and smell is big, and toxicity is big, influence pole to worker's body and environment
Greatly, smell is small, low low VOC (VOC), therefore the aqueous PP paint of environmental protection comes into being.
Patent application 201510646470.X discloses a kind of automobile exterior PP material special coating and preparation method thereof, but
The harmful substances such as toluene have been used in its priming paint, have caused VOC content higher, and film-forming temperature etc. is higher, the water resistance of sealing wax
It is also required to further increase with adhesive force.
Therefore for the coating of plastic pipe and performance requirement, it is strong to need to develop a kind of low VOC emission, quick-drying, adhesive force
And the aqueous plastic coating of function admirable is significant.
Summary of the invention
In view of the above-mentioned problems, an aspect of of the present present invention provides a kind of dedicated sealing wax of polypropylene plastics, the polypropylene plastics
Expect the combination of the second resin composition for the first resin and 25-40 weight % that the film forming matter of dedicated sealing wax is 60-75 weight %
Object,
Wherein first resin is glass transition temperature >=90 DEG C, viscosity≤60cp chlorinated polypropylene modified acrylic acid
Resin,
Second resin is glass transition temperature≤35 DEG C, viscosity >=120cp chlorinated polypropylene modified acrylic acid tree
Rouge.
Be combined in the proportional amount acrylic resin modified group of first resin and the second resin
Conjunction object, can be in conjunction with the advantages of the two as film forming matter, and the sealing wax of preparation not only has suitable film-forming temperature, drying time
It is shorter, and hardness is high, and VOC content is also low.
In certain embodiments of the present invention, first resin is SP1300, and second resin is RAC059.
In certain embodiments of the present invention, the dedicated sealing wax of the polypropylene plastics also containing 70-80 weight % first
The composition of the second dispersing agent of dispersing agent and 20-30 weight % composition is as dispersing agent, wherein first dispersing agent is amine
Value is the high molecular weight block copolymer solution of the affinity groups containing pigment of 8-12mgKOH/g, and the second dispersing agent is that amine value is 22-
The modified polyurethane of 28mgKOH/g.
First dispersing agent and the second dispersing agent, which can not only play, promotes material particles to be dispersed in medium, is formed
The effect of stable suspension, since the first dispersing agent has specific groups, additionally it is possible to it is combined well with pigment, and second
Dispersing agent is due to can be in conjunction with the polar group in polypropylene plastics and film forming matter, to increase preparation containing amine groups
The adhesive force of sealing wax.When the two is maintained at special ratios content of the present invention, the performance of various aspects can be taken into account, is had most
The effect of good raising sealing wax adhesive force.
In certain embodiments of the present invention, first dispersing agent is BYK190, and second dispersing agent is
EFKA4560。
In certain embodiments of the present invention, dipropyl of the dedicated sealing wax of the polypropylene plastics also containing 70-90 weight %
The composition of the dipropylene glycol methyl ether (DPM) of glycol butyl ether (DPNB) and 10-30 weight % composition is as cosolvent.By above-mentioned spy
The drying property for determining the dedicated sealing wax of polypropylene plastics of content and composition cosolvent preparation is better than made of other contents
The drying property of sealing wax, and its VOC content is lower.
In certain embodiments of the present invention, the dedicated sealing wax of the polypropylene plastics, the component containing following parts by weight:
38-48 parts of film forming matter, 3-5 parts of adhesion promoter, 0.3-1 parts of pH adjusting agent, 15-25 parts of deionized water, are helped
7-14 parts of solvent, 0.3-1.5 parts of dispersing agent, 0.1-0.5 parts of defoaming agent, 10-18 parts of pigment, 0.05-0.15 parts of anti-settling agent, wetting
0.1-0.8 parts of agent, 0.1-0.5 parts of levelling agent, 0.5-3 parts of thickener.
In certain embodiments of the present invention, the pH adjusting agent be AMP-95, ammonium hydroxide, one in dimethylethanolamine
Kind is several.
In certain embodiments of the present invention, the defoaming agent is organic silicon defoaming agent.
In certain embodiments of the present invention, the pigment is titanium dioxide.
In certain embodiments of the present invention, the anti-settling agent is organic vapors silica, and the wetting agent is
Organic silicon modified by polyether class compound.
In certain embodiments of the present invention, the thickener is inorganic thickener, alkali-swelling type thickener, PU are formed
One of thickener is a variety of.
Another aspect of the present invention provides a kind of preparation method of dedicated sealing wax of polypropylene plastics as described above, including such as
Lower step:
Mixing step, according to raw material proportioning by deionized water, wetting agent, pH adjusting agent, dispersing agent, defoaming agent, adhesive force
Promotor is added in stock pot, stirs to get mixed liquor A;
Pigment, anti-settling agent, cosolvent, levelling agent is added according to raw material proportioning in pulping stage in mixed liquor A, and dispersion is equal
It is even to obtain mixed liquid B, mixed liquid B is then ground to fineness less than or equal to 20 microns, obtains mill base;
The mill base and film forming matter are added in paint mixing tank by paint step, are stirred the viscosity of paint solution with thickener
Specific viscosity needed for being adjusted to, obtains semi-finished product, by the semi-finished product warp thread net filtration, obtains the dedicated sealing wax of polypropylene plastics.
The utility model has the advantages that
Polypropylene substrate coating at present is substantially oiliness PP paint, and smell is big, and toxicity is big, to worker's body and environment shadow
It rings greatly, and the adhesive force of sealing wax and other performances do not reach requirement.The polypropylene plastics dedicated water of offer of the present invention
Paint uses unique component and constitutes, not only has the comprehensive functions such as good acid and alkali-resistance, oil resistant, ageing-resistant, also hard
Degree, adhesive force, drying time etc. have extraordinary performance, and can low temperature drying, storage stability is good, application range
Extensively.And VOC is lower, and environment protection health is to human body almost without harm.
Specific embodiment
By explaining that the preferred embodiment of following the application, other objects and advantages of the present invention will be apparent.
Unless otherwise stated, all technical and scientific terms used herein has the technical field of the invention
The normally understood identical meanings of those having ordinary skill in the art.
It should be understood that it is to describe special embodiment that heretofore described term, which is only, it is not intended to limit this hair
It is bright.In addition, for the numberical range in the present invention, it is thus understood that it is also specifically disclosed that every between the upper and lower bound of the range
A median.In in the median and any other statement value in any statement value or stated ranges or in the range
Between each of between value lesser range be also included in the present invention.These small range of upper and lower bounds can independently include
Or it excludes in range.
In the present invention, described " part " is by weight.
Glass transition temperature of the present invention is measured by 19466.2 plastics differential scanning calorimetry of GB/T
's.The viscosity is to be tested by GB/T 9269-2009 with Stormer viscosmeter (KU-2 type).The VOC content presses GB
Method is tested in 18582-2008.The hardness is tested by GB/T6739-2006.The adhesive force is reference
" scratch experiment of GBT9286-1998 paint and varnish paint film " is come what is be measured.
In addition, in order to better illustrate the present invention, being given in specific embodiment below numerous specific
Details.It will be appreciated by those skilled in the art that without certain details, the present invention equally be can be implemented.In other reality
It applies in example, method well known to those skilled in the art, means is not described in detail, in order to highlight purport of the invention.
PH adjusting agent of the present invention is a kind of adjustable and control sealing wax coating pH value substance, for aqueous painting
Pigments and fillers dispersion, system stabilization and storage stabilization have meaning of crucial importance in material production process.PH adjusting agent of the present invention
It can be any substance commonly used in the art.
Wetting agent of the present invention can reduce the interfacial tension of water and pigments and fillers surface, make pigments and fillers surface be easy to by
Water wetting.Dispersing agent can soak pigments and fillers surface, while can promote the suspended dispersed of pigments and fillers particle in water.Institute of the present invention
The wetting agent stated can be any wetting agent commonly used in the art.
Aqueous inner wall paint can generate a large amount of bubbles in production and work progress due to stirring, high speed dispersion etc..
If bubble control it is bad, can make coating generate shrinkage cavity, cissing, paint face phenomena such as, seriously affect its quality and decorative effect, may be used also
The problems such as capable of causing the brushability difference and poor recoatability of coating.Therefore it need to inhibit the generation of bubble by the way that defoaming agent is added and disappear
Bubble removing, defoaming agent of the present invention are that foam is inhibited to generate or eliminate the substance for having generated foam, and this field can be used
Common any defoaming agent.
Adhesion promoter of the present invention refer to the adhesive force that coating system can be improved with wider dissolubility and
The substance of toughness.
Pigment of the present invention is that one kind has certain color and do not dissolve in using medium and can be uniformly dispersed in medium
In substance.Pigment is the important component in coating, it can not only make paint film have certain covering power, play decoration and
Protective effect, moreover it is possible to improve mechanical strength, anti-corrosive properties, light resistance and the weatherability of paint film.
Anti-settling agent of the present invention is that coating is made to have thixotropy, the substance that viscosity greatly improves.Anti-settling agent exists
It plays an important role, the production of coating, storage, coating and film performance is had an important influence on, in coating in modern coatings
Add people's anti-settling agent, i.e., introduce loose webs thixotropy structure in coating, pigments and fillers particle can be made to suspend without agglomerating, prevented
Pigment sedimentation improves coating property, keeps excellent levelability etc..
Using water as decentralized medium, viscosity is not so good as the dedicated sealing wax of polypropylene plastics of the present invention close to water, rheological characteristic
Solvent based coating, such as layering, agglomeration are easy to appear when can opening, when construction, easily occurs splashing, sagging etc., seriously affects coating
Storage, construction and quality of forming film.Therefore it to improve the viscosity of water paint, improving coating rheological property, can add a certain amount of
Thickener plays control action to the rheological behavior of emulsion paint, coating can not only be made to thicken after thickener is added, while can also assign
Its excellent mechanical performance and physical and chemical stability energy are given, such as improves thixotropy, resist sagging and storage stability.
The dedicated sealing wax of polypropylene plastics of the present invention can also include mould inhibitor, kill according to the specific needs of coating
One of microbial inoculum, coalescing agent etc. are a variety of.
Embodiment 1
The first step, mixing step, by weight, by 20 parts of deionized waters, 0.5 part of organic silicon modified by polyether wetting agent,
0.5 part of AMP-95,0.3-1.5 parts of dispersing agent be (BYK190 (amine value 12mgKOH/g) of 75 weight % and 25 weight %'s
EFKA4560 (amine value 22mgKOH/g) composition composition), 0.3 part of organic silicon defoaming agent, 4 parts of adhesion promoters
BYK-4500 is added in stock pot, stirs to get mixed liquor A.
15 parts of titanium white powder pigments, 0.1 part of organic vapors two are added in second step, pulping stage by weight in mixed liquor A
Silica anti-settling agent, 10 parts of cosolvents (composition of the DPM of the DPNB of 80 weight % and 20 weight % composition), 0.3 part of levelling
Agent Tego270 is uniformly dispersed to obtain mixed liquid B, mixed liquid B is then ground to fineness≤20 micron, obtains mill base.
Third step, paint step, by above-mentioned mill base and 40 parts of film forming matter (SP1300 (glass transition temperatures of 70 weight %
Be 90 DEG C, viscosity 60cp) and 30 weight % RAC059 (glass transition temperature is 35 DEG C, viscosity 120cp)) be added to paint
In tank, specific viscosity needed for being adjusted to the stirring of the viscosity of paint solution with thickener THIXOL53L obtains semi-finished product, will it is described partly at
Product warp thread net filtration obtains the dedicated sealing wax of polypropylene plastics 1.
Embodiment 2
The first step, mixing step, by weight, by 15 parts of deionized waters, 0.1 part of organic silicon modified by polyether wetting agent,
((amine value is the EFKA4520 of the BYK190 of 70 weight % and 30 weight % for 0.3 part of dimethylethanolamine, 0.3 part of dispersing agent
28mgKOH/g) the composition formed), 0.1 part of organic silicon defoamer, 3 parts of adhesion promoter BYK-4510 stock pots are added
In, stir to get mixed liquor A.
10 parts of titanium white powder pigments, 0.05 part of organic vapors are added in second step, pulping stage by weight in mixed liquor A
Silica anti-settling agent, 7 parts of cosolvents (composition of the DPM of the DPNB of 70 weight % and 30 weight % composition), 0.1 part of levelling
Agent EL-2826 is uniformly dispersed to obtain mixed liquid B, mixed liquid B is then ground to fineness≤20 micron, obtains mill base.
Third step, paint step, by above-mentioned mill base and 38 parts of film forming matter (alkyd resin (vitrifying temperature of 60 weight %
Degree is 95 DEG C, viscosity 50cp) and 40 weight % epoxy resin (glass transition temperature be 30 DEG C, viscosity 130cp)) be added to
In paint mixing tank, specific viscosity needed for being adjusted to the viscosity stirring of paint solution with thickener TF-1000 obtains semi-finished product, by described half
Finished product warp thread net filtration obtains the dedicated sealing wax of polypropylene plastics 2.
Embodiment 3
The first step, mixing step, by weight, by 25 parts of deionized waters, 0.8 part of organic silicon modified by polyether wetting agent, 1
Part ammonium hydroxide, the 1.5 parts of dispersing agents (EFKA4560 of the HX-3088 (amine value 8mgKOH/g) of 80 weight % and 20 weight % compositions
Composition), 0.5 part of organic silicon defoamer, 5 parts of adhesion promoter BYK-4510 be added in stock pots, stir to get mixing
Liquid A.
Second step, 18 parts of titanium white powder pigments are added by weight in mixed liquor A in pulping stage, 0.15 portion of anti-settling agent has
Machine fumed silica, 14 parts of cosolvents (composition of the DPM of the DPNB of 90 weight % and 10 weight % composition), 0.5 part of stream
Flat agent EL-2827 is uniformly dispersed to obtain mixed liquid B, mixed liquid B is then ground to fineness≤20 micron, obtains mill base.
Third step, paint step, by above-mentioned mill base and 48 parts of film forming matter (acrylic resin (vitrifyings of 75 weight %
Temperature is 93 DEG C, viscosity 45cp) and 25 weight % polyamide (glass transition temperature be 25 DEG C, viscosity 135cp)) add
Enter into paint mixing tank, specific viscosity needed for being adjusted to the viscosity stirring of paint solution with thickener TF-50TF obtains semi-finished product, by institute
Semi-finished product warp thread net filtration is stated, the dedicated sealing wax of polypropylene plastics 3 is obtained.
Embodiment 4
In addition to film forming matter is substituted for 50 weight % SP1300 and 50 weight % RAC059 composition composition it
Outside, other conditions are same as Example 1, and the dedicated sealing wax of polypropylene plastics 4 is prepared.
Embodiment 5
In addition to dispersing agent is substituted for 50 weight % BYK190 and 50 weight % EFKA4560 composition composition it
Outside, other conditions are same as Example 1, and the dedicated sealing wax of polypropylene plastics 5 is prepared.
Embodiment 6
Other than cosolvent to be substituted for the composition of the DPM of DPNB and 50 weight % of 50 weight % composition, other
Condition is same as Example 2, and the dedicated sealing wax of polypropylene plastics 6 is prepared.
Embodiment 7
In addition to film forming matter is changed into except acrylic resin (glass transition temperature is 50 DEG C, viscosity 80cp), other
Part is same as Example 2, and the dedicated sealing wax of polypropylene plastics 7 is prepared.
Embodiment 8
Other than changing dispersing agent into polyacrylic acid sodium salt (amine value 15mgKOH/g), other conditions and 1 phase of embodiment
Together, the dedicated sealing wax of polypropylene plastics 8 is prepared.
Embodiment 9
Other than changing cosolvent into isopropanol, other conditions are same as Example 1, and it is special that polypropylene plastics is prepared
With sealing wax 9.
The performance test results of above-described embodiment 1-9 are as shown in table 1.Pass through comparative example 1, embodiment 4 and embodiment 7
Test result can be seen that when the ratio of both SP1300 and RAC059 in changing film forming matter and other conditions do not change
When, the hardness for the sealing wax that embodiment 4 is prepared obviously is not so good as embodiment 1, and drying time is also more long, and VOC content slightly increases
Add, this illustrates the composition for using first resin and the second resin to form in specific content range as film forming matter
The hardness and drying property of the sealing wax prepared when matter are more preferable, and VOC content is also low.And film forming matter is changed to third in embodiment 7
The sealing wax 7 that olefin(e) acid resin is prepared, adhesive force are obviously not so good as sealing wax 1, and more long compared to its drying time of sealing wax 1, firmly
Spend worse, VOC content is also higher.The above results show the combination formed using the first resin of the present invention and the second resin
Its performance of the sealing wax prepared when object is as film forming matter is more preferable.
Pass through comparative example 1, the test result of embodiment 5 and embodiment 8, it can be seen that when dispersing agent to be changed to gather
Acrylic acid sodium salt changes and other conditions when not changing, and the adhesive force of sealing wax 1 is significantly better than sealing wax 8, this explanation uses institute of the present invention
The sealing wax that the composition of the first dispersing agent stated and the second dispersing agent composition is prepared as dispersing agent can significantly improve its attachment
Power, and other aspect property retentions are constant.Sealing wax 5 is compared with sealing wax 1, only changes the first dispersing agent and the second dispersing agent
Content, adhesive force also reduce, this illustrates that the first dispersing agent of the invention has within the scope of certain content with the second dispersing agent
There is optimal effect.
Pass through comparative example 1, the test result of embodiment 6 and embodiment 9, it can be seen that when in changing cosolvent
When the content of both dipropylene and dipropylene glycol methyl ether, the drying time of sealing wax 6 is considerably longer than sealing wax 1, this explanation is adopted
The drying time of the sealing wax prepared when using the composition of DPNB and DPM as cosolvent is longer, other performances are held essentially constant.
And having used isopropanol as cosolvent in sealing wax 9, drying time is also longer compared to sealing wax 1, and VOC content is higher, this
The drying time for the sealing wax for the composition that uses the DPNB and DPM of certain content range to form is shown as cosolvent preparing is more
Short, VOC content is lower.
Table 1
Claims (7)
1. a kind of dedicated sealing wax of polypropylene plastics, it is characterised in that:
The of the first resin and 25-30 weight % that the film forming matter of the dedicated sealing wax of polypropylene plastics is 70-75 weight %
The composition of two resins composition;The dedicated sealing wax of polypropylene plastics contains the first dispersing agent and 20-30 weight of 70-80 weight %
The composition of the second dispersing agent composition of % is measured as dispersing agent;
The dedicated sealing wax of polypropylene plastics contains the dipropylene of 70-90 weight % and the dipropyl two of 10-30 weight %
The composition of alcohol methyl ether composition is as cosolvent;
The dedicated sealing wax of polypropylene plastics is using water as decentralized medium;
The dedicated sealing wax of polypropylene plastics contains the component of following parts by weight: 38-48 parts of film forming matter, adhesion promoter 3-
5 parts, 0.3-1 parts of pH adjusting agent, 15-25 parts of deionized water, 7-14 parts of cosolvent, 0.3-1.5 parts of dispersing agent, defoaming agent 0.1-
0.5 part, 10-18 parts of pigment, 0.05-0.15 parts of anti-settling agent, 0.1-0.8 parts of wetting agent, 0.1-0.5 parts of levelling agent and thickener
0.5-3 parts;
Wherein first resin is glass transition temperature >=90 DEG C, viscosity≤60cp chlorinated polypropylene modified acrylic acid tree
Rouge, second resin are glass transition temperature≤35 DEG C, viscosity >=120cp chlorinated polypropylene modified acrylic resin;
First dispersing agent is that the high molecular weight block copolymer for the affinity groups containing pigment that amine value is 8-12mgKOH/g is molten
Liquid, second dispersing agent are the modified polyurethane that amine value is 22-28mgKOH/g.
2. the dedicated sealing wax of polypropylene plastics according to claim 1, it is characterised in that:
The pH adjusting agent is one or more of AMP-95, dimethylethanolamine and ammonium hydroxide.
3. the dedicated sealing wax of polypropylene plastics according to claim 1, it is characterised in that:
The defoaming agent is organic silicon defoaming agent.
4. the dedicated sealing wax of polypropylene plastics according to claim 1, it is characterised in that:
The pigment is titanium dioxide.
5. the dedicated sealing wax of polypropylene plastics according to claim 1, it is characterised in that:
The anti-settling agent is organic vapors silica, and/or
The wetting agent is organic silicon modified by polyether class compound.
6. the dedicated sealing wax of polypropylene plastics according to claim 1, it is characterised in that:
The thickener is one of inorganic thickener, alkali-swelling type thickener and PU association thickener or a variety of.
7. a kind of preparation method of the dedicated sealing wax of polypropylene plastics described in any one of claims 1-6, includes the following steps:
Mixing step promotes deionized water, wetting agent, pH adjusting agent, dispersing agent, defoaming agent, adhesive force according to raw material proportioning
Agent is added in stock pot, stirs to get mixed liquor A;
Pulping stage is added pigment, anti-settling agent, cosolvent, levelling agent according to raw material proportioning in mixed liquor A, is uniformly dispersed
To mixed liquid B, mixed liquid B is then ground to fineness less than or equal to 20 μm, obtains mill base;
The mill base and film forming matter are added in paint mixing tank by paint step, are adjusted to the viscosity stirring of paint solution with thickener
Required specific viscosity, obtains semi-finished product, by the semi-finished product warp thread net filtration, obtains the dedicated sealing wax of polypropylene plastics.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710018483.1A CN106833190B (en) | 2017-01-10 | 2017-01-10 | Dedicated sealing wax of polypropylene plastics and preparation method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710018483.1A CN106833190B (en) | 2017-01-10 | 2017-01-10 | Dedicated sealing wax of polypropylene plastics and preparation method thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
CN106833190A CN106833190A (en) | 2017-06-13 |
CN106833190B true CN106833190B (en) | 2019-05-31 |
Family
ID=59118620
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201710018483.1A Active CN106833190B (en) | 2017-01-10 | 2017-01-10 | Dedicated sealing wax of polypropylene plastics and preparation method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN106833190B (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107641379A (en) * | 2017-10-23 | 2018-01-30 | 河北晨阳工贸集团有限公司 | A kind of special sealing wax of bumper and its preparation, application method |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102086332A (en) * | 2009-12-03 | 2011-06-08 | 立邦涂料(中国)有限公司 | Coating composition for polyolefin substrate and coating and product thereof |
CN104356843A (en) * | 2014-10-31 | 2015-02-18 | 中科院广州化学有限公司 | Water-based composite coating material for photocuring chlorinated polypropylene-polyurethane oligomer BOPP as well as preparation and application of water-based composite coating material |
CN105199515A (en) * | 2015-10-27 | 2015-12-30 | 惠州圣源恒工艺品有限公司 | Porcelain imitation coating and spraying method thereof |
-
2017
- 2017-01-10 CN CN201710018483.1A patent/CN106833190B/en active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102086332A (en) * | 2009-12-03 | 2011-06-08 | 立邦涂料(中国)有限公司 | Coating composition for polyolefin substrate and coating and product thereof |
CN104356843A (en) * | 2014-10-31 | 2015-02-18 | 中科院广州化学有限公司 | Water-based composite coating material for photocuring chlorinated polypropylene-polyurethane oligomer BOPP as well as preparation and application of water-based composite coating material |
CN105199515A (en) * | 2015-10-27 | 2015-12-30 | 惠州圣源恒工艺品有限公司 | Porcelain imitation coating and spraying method thereof |
Also Published As
Publication number | Publication date |
---|---|
CN106833190A (en) | 2017-06-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN105086805B (en) | A kind of high hard high abrasion aqueous double-component woodenware lacquer and preparation method thereof | |
CN104592840B (en) | Mute white finish paint of a kind of high-performance water-based woodenware half of damage resistant and preparation method thereof | |
CN104962173B (en) | A kind of epoxide terrace sealing wax and preparation method thereof | |
CN105462403B (en) | A kind of composite aqueous woodenware one-component semi-gloss varnish and preparation method thereof | |
CN105315882A (en) | Water-based scratch-resistant transparent finishing coat as well as preparation method and application thereof | |
CN109135455A (en) | A kind of aqueous protective paint of high-performance water proof and wearable and preparation method thereof | |
CN105130369A (en) | Aqueous internal wall inorganic coating and preparation method thereof | |
CN105440925A (en) | Waterborne woodware surface color modifier | |
CN104559567A (en) | Finishing-free stone-like paint and preparation method thereof | |
CN109439090A (en) | A kind of corrosion-resistant quick dried environment protection water paint and preparation method thereof | |
CN106590323B (en) | Special water-based epoxy floor paint and preparation method and application thereof | |
CN110643252A (en) | Water-based epoxy floor coating and preparation method thereof | |
CN105017906A (en) | Water-in-water multi-color water paint and preparation method thereof | |
CN107384155A (en) | A kind of novel aqueous PE woodcare paints and preparation method thereof | |
CA3172225A1 (en) | Aqueous coating compositions | |
CN106833190B (en) | Dedicated sealing wax of polypropylene plastics and preparation method thereof | |
AU2017301461A1 (en) | Water based sealer with superior durability | |
CN113025147A (en) | Water-based wall surface hand-sprayed paint and preparation method thereof | |
CN107118640A (en) | A kind of seal coat and preparation method thereof | |
CN107267003A (en) | Vehicle bridge coating of waterborne organic silicon modified acroleic acid bottom surface unification and preparation method thereof | |
CN106752540A (en) | A kind of high rigidity, wear-resistant aqueous woodware paint and preparation method thereof | |
CN106046984A (en) | Water-based coating composition | |
CN106065264B (en) | A kind of high dedicated sealing wax of anti-corrosion high durable metal component and preparation method thereof | |
CN107446437A (en) | Aqueous woodware paint and preparation method thereof | |
CN115141532B (en) | Low-VOC safe and environment-friendly water-based paint and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | 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 | ||
PP01 | Preservation of patent right | ||
PP01 | Preservation of patent right |
Effective date of registration: 20200918 Granted publication date: 20190531 |
|
PD01 | Discharge of preservation of patent |
Date of cancellation: 20210715 Granted publication date: 20190531 |
|
PD01 | Discharge of preservation of patent | ||
PP01 | Preservation of patent right |
Effective date of registration: 20210715 Granted publication date: 20190531 |
|
PP01 | Preservation of patent right | ||
PD01 | Discharge of preservation of patent |
Date of cancellation: 20210926 Granted publication date: 20190531 |
|
PD01 | Discharge of preservation of patent |