CN103589294A - Acrylic acid finishing paint and preparation method thereof - Google Patents

Acrylic acid finishing paint and preparation method thereof Download PDF

Info

Publication number
CN103589294A
CN103589294A CN201310466224.7A CN201310466224A CN103589294A CN 103589294 A CN103589294 A CN 103589294A CN 201310466224 A CN201310466224 A CN 201310466224A CN 103589294 A CN103589294 A CN 103589294A
Authority
CN
China
Prior art keywords
parts
acrylic acid
hour
paint
finishing paint
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201310466224.7A
Other languages
Chinese (zh)
Inventor
朱俊伟
张剑
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.)
Wuhu Cimc Ruijiang Automobile Co Ltd
Original Assignee
Wuhu Cimc Ruijiang Automobile 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 Wuhu Cimc Ruijiang Automobile Co Ltd filed Critical Wuhu Cimc Ruijiang Automobile Co Ltd
Priority to CN201310466224.7A priority Critical patent/CN103589294A/en
Publication of CN103589294A publication Critical patent/CN103589294A/en
Pending legal-status Critical Current

Links

Landscapes

  • Paints Or Removers (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

The invention discloses an acrylic acid finishing paint. The acrylic acid finishing paint is prepared from the following raw materials in parts by weight: 50-55 parts of epoxy acrylate, 10-12 parts of trimethylolpropane triacrylate, 8-10 parts of dipentaerythritol hexaacrylate, 10-15 parts of aluminium nitride, 3-4 parts of distearoyl isopropoxy aluminate, 6-8 parts of polyisobutylene, 9-12 parts of butyl acetate, 4-5 parts of 2-hydroxy-2methyl-1phenylacetone, 3-5 parts of zinc borate and 3-4 parts of dispersing aid. The dispersing aid can be used for improving the optical property, enabling the oil paint to be uniformly dispersed and maintaining the stability of the oil paint. The acrylic acid finishing paint has very good flexibility, rust resisting property, saline-alkaline tolerance, high hardness and scratch resistance and the characteristics of high gloss, good adhesive force, excellent water resistance and the like. The acrylic acid finishing paint has good protective color and workability, is simple in preparation technology and provides protective and decorating effects for outdoor walls, steel structures, mechanical equipment, motors and the like.

Description

A kind of acrylic acid top-coat and preparation method thereof
Technical field
The present invention relates to a kind of paint and preparation method thereof, particularly a kind of acrylic acid top-coat and preparation method thereof.
Background technology
Finish paint is the final coating of application, therefore material therefor is had to higher requirement, not only to there be good colourity and brightness, more require to have good anti-pollution, ageing-resistant, protection against the tide, mildew resistance is good, also to have free from environmental pollution, safety non-toxic, fast without fire hazard, easy construction, dried coating film, protect light and protect the features such as look good, good permeability.Have and decorate and defencive function, as color, gloss, texture etc., also need the resistivity in the face of severe environment.
The single-component quick-drying finish paint that acrylic acid top-coat is comprised of thermoplastic acrylic resin, pigment, auxiliary agent, solvent etc.This paint has good tint retention and workability.For the effect that outdoor wall, steel construction, mechanical means, motor etc. provide protection and decorate, also can be used as the finish paint of embossment figure layer system.
Summary of the invention
The object of this invention is to provide the acrylic acid top-coat that a kind of sticking power is good, water tolerance is excellent.
In order to realize object of the present invention, the present invention passes through following scheme implementation:
, by the raw material of following weight part, made: epoxy acrylate 50-55, Viscoat 295 10-12, double pentaerythritol methacrylate 8-10, aluminium nitride 10-15, sec.-propyl distearyl acyl-oxygen base Aluminate 3-4, polyisobutene 6-8, N-BUTYL ACETATE 9-12, methyl-1,2-hydroxyl-2 phenyl-acetone 4-5, zinc borate 3-5, dispersing auxiliary 3-4.
Described dispersing auxiliary makes by the following method: the weight part of its each feed composition is: diatomite 200-210, nano-sized carbon 4-5, jade powder 12-13, Zinc Gluconate 2-3, xitix 1-2, pentaerythritol triacrylate 1-2, Zirconium tetrafluoride 1-2, alum 3-4, polyoxyethylene octylphenol ether 1-2, Silane coupling agent KH550 1-2; Preparation method adds diatomite in 12-15% hydrochloric acid soln and soaks 3-4 hour, takes out, and with clear water, cleans, and calcines 3-4 hour with sending in calcining furnace at 530-550 ℃, cooling, merges and grinds to form 300-400 order powder with jade; Add Zirconium tetrafluoride, nano-sized carbon, polyoxyethylene octylphenol ether to continue grinding distribution 2-3 hour, then add other remaining component to be ground to fully to disperse to obtain 300-400 order powder, obtain.
 
Acrylic acid top-coat of the present invention, by following concrete steps, made:
(1) epoxy acrylate, Viscoat 295, double pentaerythritol methacrylate, aluminium nitride are added in reactor and stirred, temperature of reaction is controlled at below 40-60 ℃, stirs 1-1.5 hour;
(2) in reactor, add sec.-propyl distearyl acyl-oxygen base Aluminate, polyisobutene, N-BUTYL ACETATE, methyl-1,2-hydroxyl-2 phenyl-acetone again, temperature of reaction is controlled at below 70-80 ℃, stirs 1 hour;
(3) finally add all the other remaining components, mix, stir, grind, obtain the slurry of 20-40 μ m, filter and get final product.
Dispersing auxiliary of the present invention has improved optical property, and paint is uniformly dispersed, and has maintained the stability of paint; The present invention has fabulous snappiness, rust-resisting property, salt tolerant alkalescence; and hardness is high, scratch resistance; there is the features such as high gloss, sticking power is good, water tolerance is excellent; the present invention has good sematic color and workability; preparation technology is simple, for outdoor wall, steel construction, mechanical means, motor etc. provide the effect of protecting and decorating.
Specific embodiments
Below by specific examples, the present invention is described in detail.
, by following weight part (kilogram) raw material make: epoxy acrylate 50, Viscoat 295 10, double pentaerythritol methacrylate 8, aluminium nitride 10, sec.-propyl distearyl acyl-oxygen base Aluminate 3, polyisobutene 6, N-BUTYL ACETATE 9, methyl-1,2-hydroxyl-2 phenyl-acetone 4, zinc borate 3, dispersing auxiliary 3.
Described dispersing auxiliary makes by the following method: the weight part of its each feed composition (kilogram) be: diatomite 200, nano-sized carbon 4, jade powder 12, Zinc Gluconate 2, xitix 1, pentaerythritol triacrylate 1, Zirconium tetrafluoride 1, alum 3, polyoxyethylene octylphenol ether 1, Silane coupling agent KH550 1; Preparation method adds diatomite in 12-15% hydrochloric acid soln and soaks 3-4 hour, takes out, and with clear water, cleans, and calcines 3-4 hour with sending in calcining furnace at 530-550 ℃, cooling, merges and grinds to form 300-400 order powder with jade; Add Zirconium tetrafluoride, nano-sized carbon, polyoxyethylene octylphenol ether to continue grinding distribution 2-3 hour, then add other remaining component to be ground to fully to disperse to obtain 300-400 order powder, obtain.
Acrylic acid top-coat of the present invention, by following concrete steps, made:
(1) epoxy acrylate, Viscoat 295, double pentaerythritol methacrylate, aluminium nitride are added in reactor and stirred, temperature of reaction is controlled at below 40-60 ℃, stirs 1-1.5 hour;
(2) in reactor, add sec.-propyl distearyl acyl-oxygen base Aluminate, polyisobutene, N-BUTYL ACETATE, methyl-1,2-hydroxyl-2 phenyl-acetone again, temperature of reaction is controlled at below 70-80 ℃, stirs 1 hour;
(3) finally add all the other remaining components, mix, stir, grind, obtain the slurry of 20-40 μ m, filter and get final product.
Product performance index of the present invention:
1, time of drying (25 ℃): surface drying 28min, does solid work 42h
2, snappiness mm≤1
3, hardness >=2H
4, high temperature resistant (130 ℃) >=490h
5, shock-resistance 50
6, salt spray resistance (120h level) >=3
7, water tolerance (29 ± 1 ℃ of 240h): non-foaming, do not come off
8, oil resistant (90# gasoline, 56h): non-foaming, do not come off
9, alkali resistance (GB/T9755-2001): by 48 hours
10, artificial weathering ageing resistance (GB/T9755-2001): by 1200 hours.

Claims (2)

1. an acrylic acid top-coat, it is characterized in that, by the raw material of following weight part, made: epoxy acrylate 50-55, Viscoat 295 10-12, double pentaerythritol methacrylate 8-10, aluminium nitride 10-15, sec.-propyl distearyl acyl-oxygen base Aluminate 3-4, polyisobutene 6-8, N-BUTYL ACETATE 9-12, methyl-1,2-hydroxyl-2 phenyl-acetone 4-5, zinc borate 3-5, dispersing auxiliary 3-4;
Described dispersing auxiliary makes by the following method: the weight part of its each feed composition is: diatomite 200-210, nano-sized carbon 4-5, jade powder 12-13, Zinc Gluconate 2-3, xitix 1-2, pentaerythritol triacrylate 1-2, Zirconium tetrafluoride 1-2, alum 3-4, polyoxyethylene octylphenol ether 1-2, Silane coupling agent KH550 1-2; Preparation method adds diatomite in 12-15% hydrochloric acid soln and soaks 3-4 hour, takes out, and with clear water, cleans, and calcines 3-4 hour with sending in calcining furnace at 530-550 ℃, cooling, merges and grinds to form 300-400 order powder with jade; Add Zirconium tetrafluoride, nano-sized carbon, polyoxyethylene octylphenol ether to continue grinding distribution 2-3 hour, then add other remaining component to be ground to fully to disperse to obtain 300-400 order powder, obtain.
2. acrylic acid top-coat according to claim 1, is characterized in that, by following concrete steps, is made:
(1) epoxy acrylate, Viscoat 295, double pentaerythritol methacrylate, aluminium nitride are added in reactor and stirred, temperature of reaction is controlled at below 40-60 ℃, stirs 1-1.5 hour;
(2) in reactor, add sec.-propyl distearyl acyl-oxygen base Aluminate, polyisobutene, N-BUTYL ACETATE, methyl-1,2-hydroxyl-2 phenyl-acetone again, temperature of reaction is controlled at below 70-80 ℃, stirs 1 hour;
(3) finally add all the other remaining components, mix, stir, grind, obtain the slurry of 20-40 μ m, filter and get final product.
CN201310466224.7A 2013-10-09 2013-10-09 Acrylic acid finishing paint and preparation method thereof Pending CN103589294A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201310466224.7A CN103589294A (en) 2013-10-09 2013-10-09 Acrylic acid finishing paint and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201310466224.7A CN103589294A (en) 2013-10-09 2013-10-09 Acrylic acid finishing paint and preparation method thereof

Publications (1)

Publication Number Publication Date
CN103589294A true CN103589294A (en) 2014-02-19

Family

ID=50079626

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201310466224.7A Pending CN103589294A (en) 2013-10-09 2013-10-09 Acrylic acid finishing paint and preparation method thereof

Country Status (1)

Country Link
CN (1) CN103589294A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104046212A (en) * 2014-05-14 2014-09-17 阜阳市美叶家具有限公司 Acid and alkali resistant heat dissipation coating
CN106676901A (en) * 2016-08-27 2017-05-17 无锡凤凰画材有限公司 High-gloss inkjet canvas and preparation method thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101412887A (en) * 2008-11-10 2009-04-22 嘉丰木业(苏州)有限公司 Floor paint
CN101935496A (en) * 2010-09-17 2011-01-05 江苏海田技术有限公司 UV (Ultraviolet)-scratch-resistant finish paint
CN103305117A (en) * 2013-06-28 2013-09-18 江苏海田技术有限公司 Ultraviolet(UV)-scratch-resistant matte finishing paint specially used for polyvinyl chloride (PVC)

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101412887A (en) * 2008-11-10 2009-04-22 嘉丰木业(苏州)有限公司 Floor paint
CN101935496A (en) * 2010-09-17 2011-01-05 江苏海田技术有限公司 UV (Ultraviolet)-scratch-resistant finish paint
CN103305117A (en) * 2013-06-28 2013-09-18 江苏海田技术有限公司 Ultraviolet(UV)-scratch-resistant matte finishing paint specially used for polyvinyl chloride (PVC)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104046212A (en) * 2014-05-14 2014-09-17 阜阳市美叶家具有限公司 Acid and alkali resistant heat dissipation coating
CN106676901A (en) * 2016-08-27 2017-05-17 无锡凤凰画材有限公司 High-gloss inkjet canvas and preparation method thereof

Similar Documents

Publication Publication Date Title
CN108753023A (en) A kind of organosilicon ceramic coating and preparation method
CN105086823A (en) Organosilicone room-temperature-cured anticorrosive coating material
CN103602183A (en) Fast-curing indentation-proof water-based paint for galvanized sheet and preparation method thereof
CN103602114A (en) Wear-resistant pressure-resistant epoxy paint and preparation method thereof
CN104449273A (en) Ultraviolet-resistant water-based paint capable of reducing brightness of coating and applied to glass door and preparation method of ultraviolet-resistant water-based paint
CN105602329A (en) Heat-reflection thermal insulation anti-corrosion coating and preparation method thereof
CN109868015A (en) A kind of organo-mineral complexing is aluminum paint, aqueous and preparation method thereof
JP5923240B2 (en) Coating material
CN103602213A (en) Anticorrosive luster primer and preparation method thereof
CN103602116A (en) High corrosion resistant epoxy paint with high solid content and preparation method thereof
CN103589294A (en) Acrylic acid finishing paint and preparation method thereof
CN104877483A (en) Anticorrosive paint for stainless steel decorating plate and preparation method of anticorrosive paint
CN107828323B (en) Metal-like coating for building exterior wall and preparation method thereof
CN104004450A (en) Switch cabinet spraying priming paint and preparation method thereof
CN105315769B (en) A kind of coloured UV ink of glass
CN104004433A (en) Flame-retardant, safe and anticorrosive paint of switch cabinet, and preparation method thereof
CN103589279A (en) Circuit board flame-retardant anti-rusting paint and preparation method thereof
CN103589288A (en) Epoxy anticorrosive paint for circuit board as well as preparation method thereof
CN103589305A (en) Finishing coat for circuit board as well as preparation method thereof
CN104327629A (en) Fouling and powdering resistant safe glass coating and its preparation method
KR101759543B1 (en) Manufacture waterproof ceramic water-based paint method and Waterproof ceramic water-based paint
CN110066586A (en) A kind of preparation method and application of water soluble acrylic acid two-component finishing coat
CN103602115A (en) Galling paint and preparation method thereof
CN104341936A (en) Wear-resistant water-based paint for glass sliding doors and preparation method thereof
CN103613967A (en) Novel magnetic epoxy primer and preparation method thereof

Legal Events

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

Application publication date: 20140219

RJ01 Rejection of invention patent application after publication