CN101643620A - Environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating and preparation method thereof - Google Patents

Environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating and preparation method thereof Download PDF

Info

Publication number
CN101643620A
CN101643620A CN200810012660A CN200810012660A CN101643620A CN 101643620 A CN101643620 A CN 101643620A CN 200810012660 A CN200810012660 A CN 200810012660A CN 200810012660 A CN200810012660 A CN 200810012660A CN 101643620 A CN101643620 A CN 101643620A
Authority
CN
China
Prior art keywords
iron oxide
micaceous iron
polyaniline
modified micaceous
environmental
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN200810012660A
Other languages
Chinese (zh)
Other versions
CN101643620B (en
Inventor
刘福春
韩恩厚
柯伟
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.)
Institute of Metal Research of CAS
Original Assignee
Institute of Metal Research of CAS
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 Institute of Metal Research of CAS filed Critical Institute of Metal Research of CAS
Priority to CN2008100126606A priority Critical patent/CN101643620B/en
Publication of CN101643620A publication Critical patent/CN101643620A/en
Application granted granted Critical
Publication of CN101643620B publication Critical patent/CN101643620B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Paints Or Removers (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)

Abstract

The invention relates to coating technology, in particular to an environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating and preparation method thereof, which solves theproblem that the prior micaceous iron oxide coating has poor anticorrosion performance, and needs to be matched with pigments containing lead and chromate during manufacturing. The environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating comprises film-forming material, polyaniline modified micaceous iron oxide, and the like. As polyaniline coating layers are formedon the surfaces of the micaceous iron oxide by an oxidative polymerization method, the treated micaceous iron oxide has the effect of passivating metal, and phytic-acid coating layers on the surfacesof the micaceous iron oxide play a role in inhibiting corrosion of metal. The environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating has strong corrosion resistance andpermeation resistance, can be applied to heavy-duty engineering of petrochemical equipment, pipelines, offshore oil platforms, wharf facilities, ships and the like.

Description

Environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating and preparation method thereof
Technical field
The present invention relates to coating technology, be specially a kind of environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating and preparation method thereof.
Background technology
Iron mica is the rational rust-stabilising pigment of the good flap of a kind of resistant to chemical media.In rust proof paint, iron mica has certain reflection potential because the overlapping accumulation of sheet has effect well water-fast and impervious to ultraviolet ray.The rust proof paint of being made by iron mica is widely used as the anti-corrosion protection of bridge, electric tower, storage tank, tank car and engineering machinery.
Chinese patent CN86104711 discloses epoxy-chlorinated chloroprene dry and wet two-way paint, be to be main binder with epoxide modified chlorination chloroprene rubber, pimelinketone-N-BUTYL ACETATE is made solvent, and iron mica, red lead powder etc. is made rust-stabilising pigment, and adopts the T31 solidifying agent.It can be used under water, the scene protection and the routine maintenance of steel equipment in alternation of wetting and drying section and the wet environment.Chinese patent CN1164552 discloses a kind of protective system and technology, the protective system of being made up of priming paint and finish paint.Wherein priming paint is made up of chlorinatedpolyethylene, clorafin, DOP, terpolycyantoamino-formaldehyde resin, iron mica, zinc chromate and other pigment.This priming paint and finish paint are applicable to outer anticorrosion and Highrise buildings water tank, food and pharmaceutical equipment anticorrosion in fields such as petrochemical complex gas tank, bridge.Chinese patent CN1164556 discloses a kind of Resins, epoxy two-component surface layer anticorrosive paint that contains pigment such as micaceous iron oxide gray, zinc yellow, iron oxide red.
Existing MIO coating existing problems: because iron mica is the physical property rust-stabilising pigment, iron and steel there is not passivation, Corrosion Protection is undesirable, must cooperate chromate pigmentss such as zinc-chrome yellow or red lead etc. to contain lead pigments, just can reach good especially anticorrosion ability.Be the protection environment, it is imperative to replace deleterious chromic salt or contain lead pigments in coating.
Summary of the invention
The object of the present invention is to provide a kind of eco-friendly polyaniline modified micaceous iron oxide anticorrosive coating and preparation method thereof, it is poor to have solved existing MIO coating antiseptic property, must be used the problem of deleterious leaded and chromate pigments in the manufacturing processed, according to polyaniline the PASSIVATION MECHANISM of iron and steel is replaced deleterious leaded and chromate pigments, reach the target that improves the MIO coating Corrosion Protection.
Technical scheme of the present invention is:
A kind of environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating, described environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating are counted by weight by following component and are constituted:
Filmogen 5~99;
Polyaniline modified micaceous iron oxide 10~45;
Pigment 1~10;
Filler 1~10;
Anti-sagging agent 0.1~4;
Dispersion agent 0.1~2;
Flow agent 0.05~2;
Defoamer 0.05~2;
Solvent 0.5~60;
Described filmogen is Synolac, resol, Resins, epoxy, urethane resin, fluorocarbon resin, supervinyi chloride resin, chlorinated rubber or chlorinatedpolyethylene etc.
Synolac can be selected short oil oleum lini glyptal, short oil oleum lini Synolac, the phenolic resin modified Synolac of short oil oleum lini, medium-oil-length Oleum Cocois Synolac, medium-oil-length ketone oil/oleum lini glyptal, medium-oil-length Thistle oil Synolac or long-oil-length tetramethylolmethane oleum lini Synolac etc. for use.
Resol can be Abietyl modified resol, pure phenolic resin or the pure dissolubility resol that alkylphenol is made.
Described Resins, epoxy is bisphenol A type epoxy resin, bisphenol f type epoxy resin or epoxy ester.Epoxy curing agent is selected amine curing agent for use.Amine curing agent is a fatty amine, as quadrol, diethylenetriamine, triethylene tetramine or tetraethylene pentamine etc.; Or aromatic amine, as mphenylenediamine or m-xylene diamine etc.; Or cycloaliphatic amines, as isophorone diamine, 4,4 '-two amido dicyclohexyl methyl hydrides, two (4-amino-3-methyl cyclohexane alkyl) methane; Or the amine modified firming agent, as amine affixture solidifying agent (fort Ao Lifu chemical industry company limited 590,591,593,810 solidifying agent of Changsha chemical institute) or mannich base (Mannich) addition polyamine curing agent (Changsha chemical institute T31, the NX-2020 of U.S. Ka Delai company, NX-2040 solidifying agent); Or the amides solidifying agent, make the polymeric amide of lacquer factory 200,300,650 or 651 models etc. as the Shanghai kairine.Urethane resin can be selected following commodity for use: Bayer (Bayer) company
Figure G2008100126606D00021
AVPLS2180FE,
Figure G2008100126606D00022
A365/1,
Figure G2008100126606D00023
A VPLS 2009/1FE,
Figure G2008100126606D00024
RD181/175X,
Figure G2008100126606D00031
A450MPA/X,
Figure G2008100126606D00032
A575FE, VPLS 2971,
Figure G2008100126606D00034
670BA,
Figure G2008100126606D00035
1652,
Figure G2008100126606D00036
A160,
Figure G2008100126606D00037
650 or 651; The FX-1560 of Deuchem Co., Ltd., FX-1660, FX-2460A, FX-2820, FX-2970A, FX-2970B, FX-3070, FX-3360, FX-4365, F-45, TN-4366, TN-4543 or PE-8043; The solidifying agent of urethane can be selected from Bayer (Bayer) company
Figure G2008100126606D00039
IL,
Figure G2008100126606D000310
N75,
Figure G2008100126606D000311
N100, N3200,
Figure G2008100126606D000313
N3390, N3300,
Figure G2008100126606D000315
VPLS2010/1,
Figure G2008100126606D000316
VPLS 2025, VPLS 2103 or
Figure G2008100126606D000318
Z4470; The Tolonate of France inferior (Rhodia) company in sieve ground TMHDB-75MX or Tolonate HDT-90; The CORONATE 2604 of Japanese polyurethane Co., Ltd., CORONATE HX-T, CORONATE 2384 or CORONATE HK.
Fluorocarbon resin can be selected following commodity for use: the fluorocarbon resin of Japan AGC Zhu Shi commercial firm commodity Lumiflon by name, as LumiflonLF-100, LumiflonLF-200 or LumiflonLF-400 etc., the ザ Off ロ Application trade mark fluorocarbon resin of Japan East Asia synthetic chemistry company, the good fortune of the new chemical industry of Xi'an Le Jia company limited
Figure G2008100126606D000319
Fluorocarbon resin, the FEVE type fluorocarbon resin of Mingzhan fluorin coating stock Co., Ltd., Dalian city; The curing agent component of fluorocarbon resin can be selected from Bayer (Bayer) company
Figure G2008100126606D000320
N75,
Figure G2008100126606D000321
N100,
Figure G2008100126606D000322
N3390,
Figure G2008100126606D000323
N3300,
Figure G2008100126606D000324
VPLS 2010/1,
Figure G2008100126606D000325
VPLS2103 or
Figure G2008100126606D000326
Z4470; The Tolonate of France inferior (Rhodia) company in sieve ground TMHDB-75MX or Tolonate TMHDT-90; The CORONATE 2604 of Nippon Polyurethane Industry Co., Ltd., CORONATE HX-T, CORONATE 2384 or CORONATE HK.The proportioning of curing agent component and modified synthetic resin component is NCO: OH=0.8-1.5: 1 (mol ratio).
Described pigment is coating pigment commonly used, as titanium dioxide, white lead, zinc oxide, phthalocyanine green, toluidine red or red iron oxide etc.; Filler is a coating filler commonly used, as ground barium sulfate, GL ground limestone, precipitated calcium carbonate, talcum powder or quartz sand etc.
Described solvent is a solvent commonly used in the preparation coating, as toluene, dimethylbenzene, butanols, butanone or pimelinketone etc.
The particle diameter of described iron mica is 200~1000 orders.
The structure of described polyaniline modified micaceous iron oxide is a sheet structure, consists of: surface coating layer is polyaniline and phytic acid, and inside is iron mica; In coating layer, polyaniline and phytic acid uniform distribution, polyaniline accounts for 50~99.98%, and phytic acid accounts for 0.02~50%.Preferable range is: polyaniline accounts for 70~99.8wt%, and phytic acid accounts for 0.2~30wt%.
Described anti-sagging agent is one of wilkinite, polynite, kaolin, aerosil or mixture.
Described dispersion agent, flow agent, defoamer are coating auxiliary agents commonly used.Dispersion agent is as Disperbyk103, Disperbyk106, Disperbyk 107, Disperbyk110, Disperbyk111, Disperbyk115, Disperbyk 163, Disperbyk 164, Disperbyk180, Disperbyk 182, Disperbyk 184, Disperbyk 190, Disperbyk191, Disperbyk192, Disperbyk184, Disperbyk2000, Anti-Terra-P, Anti-Terra-204 or the BYK-P 104S etc. of German Bi Ke chemical company (BYK Chemie); Flow agent is as BYK-353, BYK-354,355, BYK-300, BYK-306, BYK-331, BYK-359, BYK-361, BYK-357, BYK-358 or the BYK-390 etc. of the Perenol F40 of Henkel company, German Bi Ke chemical company; Defoamer is as BYK-052, BYK-053, BYK-055, BYK-057, BYK-065, BYK-065, BYK-066N, BYK-070, BYK-071, BYK-077, BYK-085 or the BYK-088 etc. of the Defom 5300,5400,5500 of the modest chemical company of moral, German Bi Ke chemical company.
The preparation method of described environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating, carry out with step in the following order:
1) preparation method of polyaniline modified micaceous iron oxide
(a) preparation phosphoric acid and phytic acid mixed aqueous solution: wherein phosphoric acid is 0.01~5 mol, is preferably 0.1~3 mol; Phytic acid is 0.01~1 mol, is preferably 0.05~0.5 mol.
(b) aniline is joined in phosphoric acid and the phytic acid mixed aqueous solution, mixed aniline concentration is: 0.01~1 mol.Be preferably 0.06~1 mol.Continue to stir (0.5~2 hour).Get phosphoric acid and phytic acid, aniline mixed aqueous solution 500ml, add 200~1000 order iron micas of 5~1000g, and stir (5~30 minutes), be pre-chilled to 0~10 ℃.
(c) aqueous solution of preparation oxygenant: the concentration of oxygenant is 0.05~5 mol in the solution.Be preferably 0.1~2 mol.The aqueous solution of oxygenant is pre-chilled to 0~10 ℃.Oxygenant can be ammonium persulphate, hydrogen peroxide, Potassium Persulphate, benzoyl peroxide or two or more mixtures.
(d) be slowly to add in 10~30 minutes in the 500ml phosphoric acid that contains iron mica and phytic acid, the aniline mixed aqueous solution (b) (c) 500ml solution in the time, 0~10 ℃ of reaction 1~8 hour, centrifugal, use distilled water wash, 80~100 ℃ of dryings are after 1~5 hour, grind with mortar, and sieve, obtain the iron mica of bottle-green 200~1000 order electrically conductive polyaniline modifications.
2) dispersion agent, flow agent, defoamer, anti-sagging agent, pigment, filler are joined in filmogen and the solvent, (10 minutes~60 minutes) stir, grind in general coating apparatus such as sand mill or three-roller then, fineness is less than discharging after 60 microns;
3) under high-speed stirring, polyaniline modified micaceous iron oxide is added 2) in the filmogen mixture in, be uniformly dispersed (high speed dispersion 20~60 minutes) obtains environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating;
4) environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating is according to the different choice corresponding curing agent of filmogen, and some filmogen does not use the solidifying agent can film forming yet.
Under normal temperature condition, solidify and form the polyaniline modified micaceous iron oxide anticorrosion coat after 7~15 days.
Advantage of the present invention is as follows:
1, adopt the present invention, the environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating of acquisition can be realized the passivation and the inhibition of metal base.
2, adopt the present invention, improved the solidity to corrosion and the permeability resistance of conventional MIO coating.
3, adopt the present invention, can replace the leaded and chromate pigments in the conventional MIO coating, prepared coating meets the environmental requirement that does not contain harmful pigment.
Environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating of the present invention is made up of filmogen, polyaniline modified micaceous iron oxide etc.Utilize oxidative polymerization method to form the coating layer of polyaniline and phytic acid on the iron mica surface, the iron mica after the processing has passivation and corrosion inhibition to metal.Environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating has very strong solidity to corrosion and permeability resistance, can be applicable to the heavy antiseptic project of petrochemical equipment, pipeline, offshore oil platform, terminal facilities, boats and ships etc.The protection in be specially adapted to that waves splash about district and tidal range district.
The performance evaluation of iron mica coating: from the coating sample for preparing, select three, and intersect cut until exposing ground at coatingsurface with special-purpose cut pen.A slice is used for reference in addition.The neutral salt spray test of the coating sample of cut adopts Japan must congratulate the ST-ISO-3 salt-fog test machine of trier Co., Ltd..The NaCl strength of solution is 3.5wt%, and test temperature is 40 ± 2 ℃, sprays continuously 500 hours, and neutral salt spray test operative norm GB1771-79 measures corrosion expansion maximum width in cut place after 500 hours salt-fog tests.
Embodiment
Unless outside specializing among the present invention, related ratio all is weight percentage or weight ratio.
Comparative example 1
0.5 part of dispersion agent (Disperbyk110), 1 part of flow agent (Perenol F40), 1 part of defoamer (Defom5300), 0.5 part of anti-sagging agent (wilkinite), 2 parts of pigment (titanium dioxide), 2 parts of fillers (ground barium sulfate), 25 parts of 325 order iron micas, join in 40 parts of Resins, epoxy (bisphenol A type epoxy resin E-51) and the 20 parts of solvents (toluene), stirred 20 minutes, in sand mill, grind then, fineness is made the component one of epoxy-mica ferric oxide coating less than discharging after 40 microns.590 type solidifying agent are dissolved in the dimethylbenzene, make the 590 model solidifying agent of 60wt%, as component two.
By weight component one: component two=100: 35, two components are mixed, four 150mm * 75mm * No. 45 surface of steel plate of 2mm of handling to the Sa2.5 level at commercial blast spray this coating twice, Air drying 15 days, use weight ratio rosin then: 60 ℃ of liquid of paraffin=1: 1 carry out edge sealing, carry out the coating performance test.The build of paint film is 400 ± 10 μ m.
Comparative example 2
0.5 part of dispersion agent (Disperbyk115), 1 part of flow agent (BYK-300), 1 part of defoamer (BYK-066N), 0.5 part of anti-sagging agent (wilkinite), 2 parts of pigment (titanium dioxide), 2 parts of fillers (ground barium sulfate), 25 parts of 325 order iron micas, join in 85 parts of Synolac (60% oil content oleum lini Synolac) and the 20 parts of solvents (toluene), stirred 20 minutes, in sand mill, grind then, fineness is made the iron mica alkydpaints less than discharging after 40 microns.
Four 150mm * 75mm * No. 45 surface of steel plate of 2mm of handling to the Sa2.5 level at commercial blast spray this coating twice, and Air drying 15 days is used weight ratio rosin then: 60 ℃ of liquid of paraffin=1: 1 carry out edge sealing, carry out the coating performance test.The build of paint film is 400 ± 10 μ m.
Comparative example 3
1 part of dispersion agent (Disperbyk180), 0.8 part of flow agent (BYK-354), 0.5 part of defoamer (Defom5300), 0.6 part of anti-sagging agent (wilkinite), 2 parts of pigment (zinc oxide), 2 parts of fillers (talcum powder), 25 parts of 325 order iron micas, join in 50 part of 2123 model resol (the prosperous gluing Science and Technology Ltd. of Shanghai Road produces) and the 20 parts of solvents (toluene), stirred 20 minutes, in sand mill, grind then, fineness is made the iron mica phenolic coating less than discharging after 40 microns.
Four 150mm * 75mm * No. 45 surface of steel plate of 2mm of handling to the Sa2.5 level at commercial blast spray this coating twice, and Air drying 15 days is used weight ratio rosin then: 60 ℃ of liquid of paraffin=1: 1 carry out edge sealing, carry out the coating performance test.The build of paint film is 400 ± 10 μ m.
Comparative example 4
1 part of dispersion agent (Disperbyk180), 0.8 part of flow agent (BYK-354), 0.5 part of defoamer (Defom5300), 0.6 part of anti-sagging agent (kaolin), 2 parts of pigment (zinc oxide), 2 parts of fillers (talcum powder), 25 parts of 325 order iron micas, join in 50 parts of Lumiflon LF-200 fluorocarbon resins and the 20 parts of solvents (methylethylketone), stirred 20 minutes, in sand mill, grind then, fineness is made the component one of iron mica fluorocarbon coating less than discharging after 40 microns.Solidifying agent
Figure G2008100126606D00061
N75 is as component two.Solidifying agent and fluorocarbon resin component are pressed NCO: OH=1: 1 (mol ratio) proportioning, stir four 150mm * 75mm * No. 45 surface of steel plate of 2mm of handling to the Sa2.5 level at commercial blast the back and spray this coating twice, Air drying 15 days, use weight ratio rosin then: 60 ℃ of liquid of paraffin=1: 1 carry out edge sealing, carry out the coating performance test.The build of paint film is 400 ± 10 μ m.
Comparative example 5
1 part of dispersion agent (Disperbyk163), 0.8 part of flow agent (BYK-354), 0.5 part of defoamer (Defom5300), 1 part of anti-sagging agent (kaolin), 5 parts of pigment (titanium dioxide), 2 parts of fillers (talcum powder), 25 parts of 325 order iron micas, join 24 parts of Hydroxylated acrylic resins
Figure G2008100126606D00071
(solid content is 60% to A365/1, the hydroxy radical content of solid resin is 2.8%) and 15 parts of solvents (vinyl acetic monomer) in, stirred 20 minutes, in sand mill, grind then, fineness is made the component one of iron mica polyurethane coating less than discharging after 40 microns.Solidifying agent
Figure G2008100126606D00072
N75 is as component two.Solidifying agent and Hydroxylated acrylic resin component are pressed NCO: OH=1.1: 1 (mol ratio) proportioning, stir four 150mm * 75mm * No. 45 surface of steel plate of 2mm of handling to the Sa2.5 level at commercial blast the back and spray this coating twice, Air drying 15 days, use weight ratio rosin then: 60 ℃ of liquid of paraffin=1: 1 carry out edge sealing, carry out the coating performance test.The build of paint film is 400 ± 10 μ m.
Embodiment 1
Prepare polyaniline modified micaceous iron oxide by the following method:
(a) preparation phosphoric acid and phytic acid mixed aqueous solution: wherein phosphoric acid is 1.5 mol; Phytic acid is 0.5 mol.
(b) aniline is joined in phosphoric acid and the phytic acid mixed aqueous solution, mixed aniline concentration is: 0.5 mol.Continue to stir 0.5 hour.Get phosphoric acid and phytic acid, aniline mixed aqueous solution 500ml, add the 325 order iron micas of 70g, and after stirring 10 minutes, be pre-chilled to 8 ℃.
(c) aqueous solution of preparation oxygenant: select benzoyl peroxide as oxygenant, the concentration of preparation benzoyl peroxide is 1.5 mol.The aqueous solution of benzoyl peroxide is pre-chilled to 8 ℃.
(d) (c) 500ml solution was slowly added in 10~30 minutes in the 500ml phosphoric acid that contains iron mica and phytic acid, the aniline mixed aqueous solution (b), 5 ℃ of reactions 3 hours, centrifugal, use distilled water wash, 90 ℃ of dryings are after 2 hours, grind with mortar, obtain the iron mica of bottle-green 325 order electrically conductive polyaniline modifications after the screening.The structure of resulting polyaniline modified micaceous iron oxide is a sheet structure, consists of: surface coating layer is polyaniline and phytic acid, and inside is iron mica; In the coating layer of present embodiment, polyaniline and phytic acid uniform distribution, polyaniline accounts for 80wt%, and phytic acid accounts for 20wt%.
0.5 part of dispersion agent (Disperbyk110), 1 part of flow agent (Perenol F40), 1 part of defoamer (Defom5300), 0.5 part of anti-sagging agent (wilkinite), 2 parts of pigment (titanium dioxide), 2 parts of fillers (ground barium sulfate), 25 parts of 325 order polyaniline modified micaceous iron oxides, join in 40 parts of Resins, epoxy (bisphenol A type epoxy resin E-51) and the 20 parts of solvents (toluene), stirred 20 minutes, in sand mill, grind then, fineness is made the component one of polyaniline modified micaceous iron oxide corrosion-resistant epoxy paint less than discharging after 40 microns.590 type solidifying agent are dissolved in the dimethylbenzene, make the 590 model solidifying agent of 60wt%, as component two.By weight component one: component two=100: 35, two components are mixed, four 150mm * 75mm * No. 45 surface of steel plate of 2mm of handling to the Sa2.5 level at commercial blast spray this coating twice, Air drying 15 days, use weight ratio rosin then: 60 ℃ of liquid of paraffin=1: 1 carry out edge sealing, carry out the coating performance test.The build of paint film is 400 ± 10 μ m.
Embodiment 2
0.5 part of dispersion agent (Disperbyk115), 1 part of flow agent (BYK-300), 1 part of defoamer (BYK-066N), 0.5 part of anti-sagging agent (wilkinite), 2 parts of pigment (titanium dioxide), 2 parts of fillers (ground barium sulfate), press 25 parts of the 325 order polyaniline modified micaceous iron oxides of embodiment 1 method preparation, join in 85 parts of Synolac (60% oil content oleum lini Synolac) and the 20 parts of solvents (toluene), stirred 20 minutes, in sand mill, grind then, fineness is made polyaniline modified micaceous iron oxide alkyd protective system less than discharging after 40 microns.Four 150mm * 75mm * No. 45 surface of steel plate of 2mm of handling to the Sa2.5 level at commercial blast spray this coating twice, and Air drying 15 days is used weight ratio rosin then: 60 ℃ of liquid of paraffin=1: 1 carry out edge sealing, carry out the coating performance test.The build of paint film is 400 ± 10 μ m.
Embodiment 3
1 part of dispersion agent (Disperbyk180), 0.8 part of flow agent (BYK-354), 0.5 part of defoamer (Defom5300), 0.6 part of anti-sagging agent (wilkinite), 2 parts of pigment (zinc oxide), 2 parts of fillers (talcum powder), press 25 parts of the 325 order polyaniline modified micaceous iron oxides of embodiment 1 method preparation, join in 50 part of 2123 model resol (the prosperous gluing Science and Technology Ltd. of Shanghai Road produces) and the 20 parts of solvents (toluene), stirred 20 minutes, in sand mill, grind then, fineness is made polyaniline modified micaceous iron oxide phenolic aldehyde protective system less than discharging after 40 microns.Four 150mm * 75mm * No. 45 surface of steel plate of 2mm of handling to the Sa2.5 level at commercial blast spray this coating twice, and Air drying 15 days is used weight ratio rosin then: 60 ℃ of liquid of paraffin=1: 1 carry out edge sealing, carry out the coating performance test.The build of paint film is 400 ± 10 μ m.
Embodiment 4
Prepare polyaniline modified micaceous iron oxide by the following method:
(a) preparation phosphoric acid and phytic acid mixed aqueous solution: wherein phosphoric acid is 0.5 mol; Phytic acid is 0.1 mol.
(b) aniline is joined in phosphoric acid and the phytic acid mixed aqueous solution, mixed aniline concentration is: 0.1 mol.Continue to stir 1.5 hours.Get phosphoric acid and phytic acid, aniline mixed aqueous solution 500ml, add the 325 order iron micas of 20g, and after stirring 25 minutes, be pre-chilled to 2 ℃.
(c) aqueous solution of preparation oxygenant: select ammonium persulphate as oxygenant, the concentration of preparation ammonium persulphate is 0.5 mol.The aqueous solution of ammonium persulphate is pre-chilled to 2 ℃.
(d) (c) 500ml solution was slowly added in 10~30 minutes in the 500ml phosphoric acid that contains iron mica and phytic acid, the aniline mixed aqueous solution (b), 2 ℃ of reactions 1 hour, centrifugal, use distilled water wash, 80 ℃ of dryings are after 5 hours, grind with mortar, obtain the iron mica of bottle-green 325 order electrically conductive polyaniline modifications after the screening.The structure of resulting polyaniline modified micaceous iron oxide is a sheet structure, consists of: surface coating layer is polyaniline and phytic acid, and inside is iron mica; In the coating layer of present embodiment, polyaniline and phytic acid uniform distribution, polyaniline accounts for 90wt%, and phytic acid accounts for 10wt%.
1 part of dispersion agent (Disperbyk180), 0.8 part of flow agent (BYK-354), 0.5 part of defoamer (Defom5300), 0.6 part of anti-sagging agent (kaolin), 2 parts of pigment (zinc oxide), 2 parts of fillers (talcum powder), 25 parts of 325 order iron micas, join in 50 parts of Lumiflon LF-200 fluorocarbon resins and the 20 parts of solvents (methylethylketone), stirred 20 minutes, in sand mill, grind then, fineness is made the component one of polyaniline modified micaceous iron oxide fluorine carbon protective system less than discharging after 40 microns.Solidifying agent
Figure G2008100126606D00091
N75 is as component two.Solidifying agent and fluorocarbon resin component are pressed NCO: OH=1: 1 (mol ratio) proportioning, stir four 150mm * 75mm * No. 45 surface of steel plate of 2mm of handling to the Sa2.5 level at commercial blast the back and spray this coating twice, Air drying 15 days, use weight ratio rosin then: 60 ℃ of liquid of paraffin=1: 1 carry out edge sealing, carry out the coating performance test.The build of paint film is 400 ± 10 μ m.
Embodiment 5
1 part of dispersion agent (Disperbyk163), 0.8 part of flow agent (BYK-354), 0.5 part of defoamer (Defom5300), 1 part of anti-sagging agent (kaolin), 5 parts of pigment (titanium dioxide), 2 parts of fillers (talcum powder), press 25 parts of the 325 order polyaniline modified micaceous iron oxides of embodiment 4 methods preparations, join 24 parts of Hydroxylated acrylic resins (solid content is 60% to A365/1, the hydroxy radical content of solid resin is 2.8%) and 15 parts of solvents (vinyl acetic monomer) in, stirred 20 minutes, in sand mill, grind then, fineness is made the component one of polyaniline modified micaceous iron oxide anti-corrosion polyurethane coating less than discharging after 40 microns.Solidifying agent
Figure G2008100126606D00101
N75 is as component two.Solidifying agent and Hydroxylated acrylic resin component are pressed NCO: OH=1.1: 1 (mol ratio) proportioning, stir four 150mm * 75mm * No. 45 surface of steel plate of 2mm of handling to the Sa2.5 level at commercial blast the back and spray this coating twice, Air drying 15 days, use weight ratio rosin then: 60 ℃ of liquid of paraffin=1: 1 carry out edge sealing, carry out the coating performance test.The build of paint film is 400 ± 10 μ m.
The performance evaluation table of table 1 micaceous iron oxide anticorrosive coating
Cut place corrosion expansion maximum width, mm
Comparative example 1 ??2.8
Comparative example 2 ??2.4
Comparative example 3 ??2.5
Comparative example 4 ??2.2
Comparative example 5 ??1.9
Embodiment 1 ??1.1
Embodiment 2 ??1.0
Embodiment 3 ??1.2
Embodiment 4 ??1.1
Embodiment 5 ??0.9
Illustrate: according to the test-results of table 1, embodiment compares with corresponding comparative example, and corrosion extension width in cut place obviously narrows down, and shows the solidity to corrosion that has significantly been increased common MIO coating by polyaniline-modified iron mica.
Because the solidity to corrosion of environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating obviously is better than conventional micaceous iron oxide anticorrosive coating, it can the really heavy rot-resistant effect of performance under rigorous environment.And overcome the shortcoming that has harmful rust-stabilising pigment in the prior art.The environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating of being invented utilizes polyaniline and phytic acid can make metal base such as iron and steel produce the effect of passivation and inhibition, makes environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating have good solidity to corrosion.Polyaniline-modified iron mica and resin compatible are good, chemically stable.

Claims (5)

1, a kind of environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating is characterized in that, described environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating is counted by weight by following component and constituted:
Filmogen 5~99;
Polyaniline modified micaceous iron oxide 10~45;
Pigment 1~10;
Filler 1~10;
Anti-sagging agent 0.1~4;
Dispersion agent 0.1~2;
Flow agent 0.05~2;
Defoamer 0.05~2;
Solvent 0.5~60.
2, environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating according to claim 1 is characterized in that: described filmogen is Synolac, resol, Resins, epoxy, urethane resin, fluorocarbon resin, supervinyi chloride resin, chlorinated rubber or chlorinatedpolyethylene.
3, environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating according to claim 1 is characterized in that: the particle diameter of described iron mica is 200~1000 orders.
4, environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating according to claim 1, it is characterized in that: the structure of described polyaniline modified micaceous iron oxide is a sheet structure, consist of: surface coating layer is polyaniline and phytic acid, and inside is iron mica; In coating layer, polyaniline and phytic acid uniform distribution, polyaniline accounts for 50~99.98wt%, and phytic acid accounts for 0.02~50wt%.
5, the preparation method of environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating according to claim 1 is characterized in that, carries out with step in the following order:
1) preparation method of polyaniline modified micaceous iron oxide
(a) preparation phosphoric acid and phytic acid mixed aqueous solution: wherein, phosphoric acid is 0.01~5 mol, and phytic acid is 0.01~1 mol;
(b) aniline is joined in phosphoric acid and the phytic acid mixed aqueous solution, mixed aniline concentration is: 0.01~1 mol, continue to stir; Get phosphoric acid and phytic acid, aniline mixed aqueous solution 500ml, add 200~1000 order iron micas of 5~1000g, and after stirring, be pre-chilled to 0~10 ℃;
(c) aqueous solution of preparation oxygenant: the concentration of oxygenant is 0.05~5 mol in the solution, and the aqueous solution of oxygenant is pre-chilled to 0~10 ℃; Oxygenant is ammonium persulphate, hydrogen peroxide, Potassium Persulphate, benzoyl peroxide or two or more mixtures;
(d) be to add in 10~30 minutes in the 500ml phosphoric acid contain iron mica and phytic acid, the aniline mixed aqueous solution (b) (c) 500ml solution in the time, 0~10 ℃ of reaction 1~8 hour, centrifugal, use distilled water wash, 80~100 ℃ of dryings are after 1~5 hour, grind with mortar, and sieve, obtain the iron mica of bottle-green 200~1000 order electrically conductive polyaniline modifications;
2) dispersion agent, flow agent, defoamer, anti-sagging agent, pigment, filler are joined in filmogen and the solvent, stir, grind in general coating apparatus then, fineness is less than discharging after 60 microns;
3) under agitation polyaniline modified micaceous iron oxide is added 2) in the filmogen mixture in, be uniformly dispersed, obtain environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating.
CN2008100126606A 2008-08-06 2008-08-06 Environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating and preparation method thereof Active CN101643620B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2008100126606A CN101643620B (en) 2008-08-06 2008-08-06 Environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2008100126606A CN101643620B (en) 2008-08-06 2008-08-06 Environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating and preparation method thereof

Publications (2)

Publication Number Publication Date
CN101643620A true CN101643620A (en) 2010-02-10
CN101643620B CN101643620B (en) 2012-02-08

Family

ID=41655685

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2008100126606A Active CN101643620B (en) 2008-08-06 2008-08-06 Environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating and preparation method thereof

Country Status (1)

Country Link
CN (1) CN101643620B (en)

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102408787A (en) * 2011-11-09 2012-04-11 江苏兰陵高分子材料有限公司 Environment-friendly primer and top-coat integrated coating special for coal machine and preparation process for coating
CN102604533A (en) * 2012-03-14 2012-07-25 哈尔滨工程大学 Polyaniline-graphene composite based anticorrosive paint and preparation method thereof
CN102634276A (en) * 2012-04-25 2012-08-15 厦门大学 Heavy-duty anticorrosive polyaniline coating and preparation method thereof
CN102690570A (en) * 2012-06-12 2012-09-26 杨晓锋 Preparation method of water-based metal anticorrosive paint
CN102702901A (en) * 2012-06-08 2012-10-03 蒋涛 Water-based metal anticorrosive paint
CN102850919A (en) * 2012-09-14 2013-01-02 黄宣斐 Environment-friendly steel surface anticorrosive paint
CN102850918A (en) * 2012-09-14 2013-01-02 虞海香 Steel surface anticorrosive paint
CN102850917A (en) * 2012-09-14 2013-01-02 虞海香 Method for preparing anti-corrosive coating on steel surface
CN102863881A (en) * 2012-09-14 2013-01-09 黄宣斐 Steel-surface environment-friendly anticorrosive paint and preparation method thereof
CN102863883A (en) * 2012-09-14 2013-01-09 虞海盈 Preparation method of environment-friendly steel-surface anticorrosive paint
CN102863882A (en) * 2012-09-14 2013-01-09 虞海盈 Environment-friendly steel-iron surface anti-corrosion coating
CN104098996A (en) * 2014-07-21 2014-10-15 裕祥化工(大连)有限公司 Nano-composite PU (polyurethane) aircraft coating and preparation method thereof
CN105086039A (en) * 2015-09-18 2015-11-25 合肥海畅电气技术有限公司 Voltmeter with corrosion resistance
CN106118403A (en) * 2016-07-28 2016-11-16 江苏昌悦重工科技有限公司 Photovoltaic DC-to-AC converter molding box
CN106280550A (en) * 2016-07-19 2017-01-04 浙江凯色丽科技发展有限公司 Glass flake base anti-corrosion paint and preparation method thereof
CN106634435A (en) * 2016-12-21 2017-05-10 康乃尔化学工业股份有限公司 Eigenstate polyaniline coating special for corrosion prevention of oil field pipeline and preparation method of eigenstate polyaniline coating
CN106823538A (en) * 2016-12-28 2017-06-13 芜湖顺景自动化设备有限公司 A kind of high efficiency particulate air filter equipment with anticorrosive coat
CN104817902B (en) * 2015-05-20 2017-07-07 中国航发北京航空材料研究院 A kind of heat-resisting fluorine carbon anticorrosive paint and preparation method thereof
CN107400383A (en) * 2016-05-19 2017-11-28 福建坤彩材料科技股份有限公司 One kind is directly used in electrostatic powder coating pearlescent pigment and preparation method thereof
CN115975473A (en) * 2022-12-12 2023-04-18 江苏九天光电科技有限公司 Cold-rolled steel strip with heat dissipation function and processing technology thereof

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1061672C (en) * 1997-03-11 2001-02-07 连云港港务局 Two-component surface layer anticorrosive paint based on epoxy resin and its preparing method
CN100506935C (en) * 2005-12-22 2009-07-01 刘赞成 Metal corrosion resistant coating and its manufacturing process

Cited By (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102408787B (en) * 2011-11-09 2013-08-14 江苏兰陵高分子材料有限公司 Environment-friendly primer and top-coat integrated coating special for coal machine and preparation process for coating
CN102408787A (en) * 2011-11-09 2012-04-11 江苏兰陵高分子材料有限公司 Environment-friendly primer and top-coat integrated coating special for coal machine and preparation process for coating
CN102604533A (en) * 2012-03-14 2012-07-25 哈尔滨工程大学 Polyaniline-graphene composite based anticorrosive paint and preparation method thereof
CN102634276A (en) * 2012-04-25 2012-08-15 厦门大学 Heavy-duty anticorrosive polyaniline coating and preparation method thereof
CN102634276B (en) * 2012-04-25 2015-06-10 厦门大学 Heavy-duty anticorrosive polyaniline coating and preparation method thereof
CN102702901A (en) * 2012-06-08 2012-10-03 蒋涛 Water-based metal anticorrosive paint
CN102690570A (en) * 2012-06-12 2012-09-26 杨晓锋 Preparation method of water-based metal anticorrosive paint
CN102850918A (en) * 2012-09-14 2013-01-02 虞海香 Steel surface anticorrosive paint
CN102863881A (en) * 2012-09-14 2013-01-09 黄宣斐 Steel-surface environment-friendly anticorrosive paint and preparation method thereof
CN102863883A (en) * 2012-09-14 2013-01-09 虞海盈 Preparation method of environment-friendly steel-surface anticorrosive paint
CN102863882A (en) * 2012-09-14 2013-01-09 虞海盈 Environment-friendly steel-iron surface anti-corrosion coating
CN102850917A (en) * 2012-09-14 2013-01-02 虞海香 Method for preparing anti-corrosive coating on steel surface
CN102850919A (en) * 2012-09-14 2013-01-02 黄宣斐 Environment-friendly steel surface anticorrosive paint
CN104098996A (en) * 2014-07-21 2014-10-15 裕祥化工(大连)有限公司 Nano-composite PU (polyurethane) aircraft coating and preparation method thereof
CN104098996B (en) * 2014-07-21 2016-07-06 裕祥化工(大连)有限公司 A kind of nano compound polyurethane aircraft coating and preparation method thereof
CN104817902B (en) * 2015-05-20 2017-07-07 中国航发北京航空材料研究院 A kind of heat-resisting fluorine carbon anticorrosive paint and preparation method thereof
CN105086039A (en) * 2015-09-18 2015-11-25 合肥海畅电气技术有限公司 Voltmeter with corrosion resistance
CN107400383A (en) * 2016-05-19 2017-11-28 福建坤彩材料科技股份有限公司 One kind is directly used in electrostatic powder coating pearlescent pigment and preparation method thereof
CN107400383B (en) * 2016-05-19 2019-08-02 福建坤彩材料科技股份有限公司 One kind being directly used in electrostatic powder coating pearlescent pigment and preparation method thereof
CN106280550A (en) * 2016-07-19 2017-01-04 浙江凯色丽科技发展有限公司 Glass flake base anti-corrosion paint and preparation method thereof
CN106280550B (en) * 2016-07-19 2018-08-28 浙江凯色丽科技发展有限公司 Glass flake base anti-corrosion paint and preparation method thereof
CN106118403A (en) * 2016-07-28 2016-11-16 江苏昌悦重工科技有限公司 Photovoltaic DC-to-AC converter molding box
CN106634435A (en) * 2016-12-21 2017-05-10 康乃尔化学工业股份有限公司 Eigenstate polyaniline coating special for corrosion prevention of oil field pipeline and preparation method of eigenstate polyaniline coating
CN106823538A (en) * 2016-12-28 2017-06-13 芜湖顺景自动化设备有限公司 A kind of high efficiency particulate air filter equipment with anticorrosive coat
CN115975473A (en) * 2022-12-12 2023-04-18 江苏九天光电科技有限公司 Cold-rolled steel strip with heat dissipation function and processing technology thereof
CN115975473B (en) * 2022-12-12 2023-10-17 江苏九天光电科技有限公司 Cold-rolled steel strip with heat dissipation function and processing technology thereof

Also Published As

Publication number Publication date
CN101643620B (en) 2012-02-08

Similar Documents

Publication Publication Date Title
CN101643620B (en) Environmental-friendly polyaniline modified micaceous iron oxide anticorrosive coating and preparation method thereof
CN101643619B (en) Environment-friendly polyaniline modified aluminium powder anti-corrosive coating and preparation method thereof
CN101643618B (en) Non-toxic polyaniline modified anti-corrosive coating and preparation method thereof
CN101643615B (en) Polyaniline modified glass flake heavy-duty anti-corrosive coating and preparation method thereof
CN101747825B (en) Environment-friendly solvent-free humidified and rusted anticorrosive paint
CN102618148B (en) Epoxy coating and preparation method and application thereof
CN101824265A (en) Low-surface treatment moisture cured heavy anti-corrosion coating
CN101792285A (en) Chromium-free environment-friendly epoxy anticorrosion primer
CN103980797A (en) Polyurethane modified epoxy resin anticorrosive nano-coating
CN110982380A (en) Water-based epoxy resin cabin coating and preparation method thereof
CN103834209B (en) A kind of polyaniline paint and preparation method thereof hindering control chloride permeability
CN114196290A (en) Industrial water-based paint coating and application method thereof
CN110564264A (en) Water-based solvent-free epoxy anticorrosive paint and preparation method thereof
CN102786862A (en) Multifunctional epoxy primer for offshore platforms and manufacturing method thereof
CN1986711A (en) Acid-proof wear-proof anticorrosive paint and its preparing method
CN109880484A (en) A kind of water-base epoxy thickness slurry anti-decaying paint and its preparation method and application
CN105038545A (en) Heavy-duty anti-corrosive modified poly-urea coating and preparation method thereof
CN110437696A (en) Single-component water-based graphene anticorrosive paint, preparation method and application
CN108795222A (en) High Performance Corrosion Protective Coatings for ship power axis non-working surface
CN103360903A (en) Waterborne epoxy phosphatic zinc dust antirust paint and its preparation method
CN103980799B (en) There is rusty scale convert and the epoxy selfreparing on rust paint of Stabilization
CN113292912A (en) Heavy-duty anticorrosive water-based paint for ocean engineering equipment and preparation method thereof
CN110628028B (en) Preparation and application of organic silicon modified cardanol polyglycidyl ether resin
CN115746659B (en) High-solid wear-resistant epoxy glass flake coating and preparation method thereof
CN108409932A (en) A kind of preparation method of modified epoxy and its application in anticorrosive paint

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