CN110317478B - A kind of polythiophene modified cold coating zinc coating and preparation method thereof - Google Patents
A kind of polythiophene modified cold coating zinc coating and preparation method thereof Download PDFInfo
- Publication number
- CN110317478B CN110317478B CN201910533478.3A CN201910533478A CN110317478B CN 110317478 B CN110317478 B CN 110317478B CN 201910533478 A CN201910533478 A CN 201910533478A CN 110317478 B CN110317478 B CN 110317478B
- Authority
- CN
- China
- Prior art keywords
- coating
- powder
- polythiophene
- zinc
- modified
- 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
- 238000000576 coating method Methods 0.000 title claims abstract description 84
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 title claims abstract description 82
- 239000011248 coating agent Substances 0.000 title claims abstract description 78
- 229920000123 polythiophene Polymers 0.000 title claims abstract description 42
- 229910052725 zinc Inorganic materials 0.000 title claims abstract description 32
- 239000011701 zinc Substances 0.000 title claims abstract description 32
- 238000002360 preparation method Methods 0.000 title claims abstract description 9
- 239000002904 solvent Substances 0.000 claims abstract description 19
- 239000007864 aqueous solution Substances 0.000 claims abstract description 17
- 239000004925 Acrylic resin Substances 0.000 claims abstract description 9
- 229920000178 Acrylic resin Polymers 0.000 claims abstract description 9
- 239000012752 auxiliary agent Substances 0.000 claims abstract description 6
- 239000000843 powder Substances 0.000 claims description 31
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 claims description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 19
- 229920001467 poly(styrenesulfonates) Polymers 0.000 claims description 13
- 229940006186 sodium polystyrene sulfonate Drugs 0.000 claims description 13
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 12
- 239000004793 Polystyrene Substances 0.000 claims description 12
- 229920002223 polystyrene Polymers 0.000 claims description 12
- 229910052708 sodium Inorganic materials 0.000 claims description 12
- 239000011734 sodium Substances 0.000 claims description 12
- 238000001914 filtration Methods 0.000 claims description 7
- 238000001035 drying Methods 0.000 claims description 6
- 238000000227 grinding Methods 0.000 claims description 6
- 239000000376 reactant Substances 0.000 claims description 6
- 239000000243 solution Substances 0.000 claims description 6
- 238000003756 stirring Methods 0.000 claims description 6
- 238000007599 discharging Methods 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 3
- 238000005260 corrosion Methods 0.000 abstract description 15
- 230000007797 corrosion Effects 0.000 abstract description 11
- 238000004210 cathodic protection Methods 0.000 abstract description 8
- 229910000831 Steel Inorganic materials 0.000 abstract description 5
- 238000012986 modification Methods 0.000 abstract description 5
- 230000004048 modification Effects 0.000 abstract description 5
- 239000010959 steel Substances 0.000 abstract description 5
- 230000005540 biological transmission Effects 0.000 abstract description 2
- 230000009466 transformation Effects 0.000 abstract description 2
- 230000002035 prolonged effect Effects 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- 239000008367 deionised water Substances 0.000 description 13
- 229910021641 deionized water Inorganic materials 0.000 description 13
- 239000003795 chemical substances by application Substances 0.000 description 12
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 7
- 239000002270 dispersing agent Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 239000002518 antifoaming agent Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 238000005246 galvanizing Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical class O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- FYGHSUNMUKGBRK-UHFFFAOYSA-N 1,2,3-trimethylbenzene Chemical compound CC1=CC=CC(C)=C1C FYGHSUNMUKGBRK-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- HSJPMRKMPBAUAU-UHFFFAOYSA-N cerium(3+);trinitrate Chemical compound [Ce+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O HSJPMRKMPBAUAU-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- PWSZACWUDDFZMQ-UHFFFAOYSA-N 2,4-Diphenyl-1-butene Chemical compound C=1C=CC=CC=1C(=C)CCC1=CC=CC=C1 PWSZACWUDDFZMQ-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- JIAARYAFYJHUJI-UHFFFAOYSA-L Zinc chloride Inorganic materials [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- -1 bentone SD-1 Chemical class 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- ZOMNIUBKTOKEHS-UHFFFAOYSA-L dimercury dichloride Chemical class Cl[Hg][Hg]Cl ZOMNIUBKTOKEHS-UHFFFAOYSA-L 0.000 description 1
- 238000000840 electrochemical analysis Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- FYDKNKUEBJQCCN-UHFFFAOYSA-N lanthanum(3+);trinitrate Chemical compound [La+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O FYDKNKUEBJQCCN-UHFFFAOYSA-N 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 238000002161 passivation Methods 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229940007718 zinc hydroxide Drugs 0.000 description 1
- 229910021511 zinc hydroxide Inorganic materials 0.000 description 1
- 239000011787 zinc oxide 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
- C09D1/00—Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances
-
- 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/08—Anti-corrosive paints
- C09D5/10—Anti-corrosive paints containing metal dust
- C09D5/106—Anti-corrosive paints containing metal dust containing Zn
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Paints Or Removers (AREA)
Abstract
本发明涉及一种聚噻吩改性冷涂锌涂料及其制备方法，属涂料领域。按质量份数计，该聚噻吩改性冷涂锌涂料由2～30份丙烯酸树脂、0.1～6份助剂、70～98份锌粉和2～60份溶剂组成。其中，锌粉为经过聚噻吩改性处理的改性锌粉。锌粉经过聚噻吩水溶液改性处理后，可以延长涂层阴极保护作用时间，并提高涂层的耐腐蚀性能。本发明聚噻吩改性冷涂锌涂料可广泛应用于钢结构的防腐蚀工程，能够方便、快捷地解决输变电设施、高铁设施、公路设施等的腐蚀防护问题。The invention relates to a polythiophene modified cold-coated zinc coating and a preparation method thereof, belonging to the field of coatings. In parts by mass, the polythiophene-modified cold-coated zinc coating consists of 2-30 parts of acrylic resin, 0.1-6 parts of auxiliary agent, 70-98 parts of zinc powder and 2-60 parts of solvent. Wherein, the zinc powder is modified zinc powder treated by polythiophene modification. After the zinc powder is modified by the polythiophene aqueous solution, the cathodic protection time of the coating can be prolonged and the corrosion resistance of the coating can be improved. The polythiophene-modified cold-coated zinc coating of the invention can be widely used in anti-corrosion engineering of steel structures, and can solve the corrosion protection problems of power transmission and transformation facilities, high-speed rail facilities, highway facilities and the like conveniently and quickly.
Description
Technical Field
The invention relates to a polythiophene modified cold-coating zinc coating and a preparation method thereof, belonging to the field of coatings.
Background
The cold-coating zinc coating has high solid content, belongs to high-solid coating, and is environment-friendly coating. The content of zinc powder in the cold-coating zinc coating reaches more than 95 percent, and the high-content zinc powder plays a role in cathodic protection on a steel substrate in a coating and protects the steel from corrosion. How the cathodic protection of zinc powders can be extended is therefore directly related to the protection period of cold-applied zinc coatings. Many researchers have conducted much research in this regard, but with little success. Bases [ Progress in Organic Coatings,63(2008) 282-; the surface modification of zinc powder is carried out by using corrosion inhibitors such as cerium nitrate, lanthanum nitrate, benzotriazole and the like by Progress in Organic Coatings,69(2010)184-192 and the like, but the results show that the protective performance of the coating is not effectively improved.
Disclosure of Invention
Aiming at the defect of short cathodic protection action time of the existing cold-coating zinc coating, the invention aims to provide a polythiophene modified cold-coating zinc coating and a preparation method thereof, which can obviously improve the cathodic protection action of the cold-coating zinc coating.
The technical scheme of the invention is as follows:
the polythiophene modified cold-coating zinc coating comprises the following components in parts by weight:
the zinc powder is modified zinc powder subjected to polythiophene modification treatment.
The zinc powder of the polythiophene modified cold-coating zinc coating is modified by a polythiophene aqueous solution, and the content of polythiophene in the polythiophene aqueous solution is 0.3-20 wt%.
The polythiophene modified cold-coating zinc coating is characterized in that zinc powder is obtained by modifying poly (3, 4-ethylenedioxythiophene) aqueous solution, and the content of poly (3, 4-ethylenedioxythiophene) in the poly (3, 4-ethylenedioxythiophene) aqueous solution is 0.3-20 wt%.
The polythiophene modified cold-coating zinc coating is characterized in that zinc powder is modified by a sodium polystyrene sulfonate-doped polythiophene aqueous solution, the content of sodium polystyrene sulfonate-doped polythiophene in the sodium polystyrene sulfonate-doped polythiophene aqueous solution is 0.3-20 wt%, and the doping amount of the sodium polystyrene sulfonate is 100-2500 wt% of polythiophene.
The polythiophene modified cold-coating zinc paint is characterized in that zinc powder is modified by a sodium polystyrene sulfonate-doped poly (3, 4-ethylenedioxythiophene) aqueous solution, the content of the sodium polystyrene sulfonate-doped poly (3, 4-ethylenedioxythiophene) in the sodium polystyrene sulfonate-doped poly (3, 4-ethylenedioxythiophene) aqueous solution is 0.3-20 wt%, and the doping amount of the sodium polystyrene sulfonate is 100-2500 wt% of the poly (3, 4-ethylenedioxythiophene).
The preparation method of the polythiophene modified cold-coating zinc coating comprises the following steps:
(1) adding a solvent into a reaction kettle, adding a polythiophene aqueous solution with the mass of 0.5-20% of that of the solvent in a stirring state, adding zinc powder according to 10-70% of that of the solvent, heating to 20-50 ℃, and reacting for 0.5-3 h; centrifuging the reactant, taking out the powder, rinsing the powder for 2-5 times by using a solvent, drying the powder for 10-24 hours at the temperature of 40-70 ℃, and grinding the powder into powder to prepare modified zinc powder;
(2) adding acrylic resin, a solvent and an auxiliary agent into a reaction kettle in sequence, and dispersing for 15-50 min at the rotating speed of 300-1000 rpm; then adding modified zinc powder, dispersing at 300-1000 rpm for 30-100 min, filtering and discharging to obtain the polythiophene modified cold-coating zinc coating.
The design idea of the invention is as follows:
the zinc powder in the cold-coated zinc coating reacts with a corrosive medium (water, chloride ions and the like) to generate zinc oxide, hydroxide or chloride, so the surface modification of the zinc powder is needed to improve the self-corrosion speed of the zinc powder in the corrosive medium, but the treated zinc powder also has conductivity and does not influence the play of the cathode protection effect of the zinc powder. Therefore, the invention uses polythiophene to carry out coating treatment on the surface of the zinc powder, reduces the self-corrosion speed of the zinc powder and prolongs the cathodic protection time of the cold-coating zinc coating.
The invention has the following advantages and beneficial effects:
1. after the zinc powder is coated by polythiophene, the dispersibility of the zinc powder is improved, and the compatibility with resin is improved.
2. After the zinc powder is subjected to polythiophene coating treatment, the storage stability of the cold-coating zinc coating is obviously improved.
3. After the zinc powder is subjected to polythiophene coating treatment, the cathode protection effect of the coating is obviously improved.
4. The invention adopts the polythiophene to lead the steel surface to enter a passivation state, and improves the corrosion protection effect of the cold-coating zinc coating.
5. The method is suitable for large-scale production of the polythiophene modified cold-coating zinc coating, the polythiophene modified cold-coating zinc coating can be widely applied to the anti-corrosion engineering of a steel structure, and the corrosion protection problems of power transmission and transformation facilities, high-speed rail facilities, highway facilities and the like can be conveniently and quickly solved.
Detailed Description
In a specific embodiment, the polythiophene modified cold-coating zinc coating comprises the following components in parts by weight:
wherein, the zinc powder can be micron-sized zinc powder with the granularity of 1-50 μm. The zinc powder is modified by polythiophene aqueous solution, and the content of polythiophene in the polythiophene aqueous solution is 0.3-20% (preferably 0.5-15%). The polythiophene is preferably poly (3, 4-ethylenedioxythiophene), the poly (3, 4-ethylenedioxythiophene) is preferably poly (3, 4-ethylenedioxythiophene) doped with sodium polystyrene sulfonate, and the doping amount of the sodium polystyrene sulfonate is 100 to 2500 weight percent of the poly (3, 4-ethylenedioxythiophene). The solvent refers to a solvent commonly used in preparing the coating, such as: deionized water, xylene, toluene, trimethylbenzene or butyl acetate, etc. The auxiliary agent is a dispersing agent, a defoaming agent, a leveling agent and an anti-settling agent commonly used for the coating, and the dispersing agent is as follows: disperbyk-108, Disperbyk-111, Disperbyk-115, Disperbyk-140 from BYK, Germany. Defoamers such as: BYK-012, BYK-014, BYK-055, BYK-066N of BYK, Germany. Leveling agents such as: EFKA 3030, EFKA 3033, EFKA 3600N or EFKA 3772N of Ciba, Netherlands. The anti-settling agent can be selected from organically modified bentonite, such as: bentone SD-1, Bentone SD-2, Bentone 27, Bentone 34 or Bentone 52.
The preparation method of the polythiophene modified cold-coating zinc coating comprises the following steps:
(1) preparation of modified zinc powder
Adding a solvent into a reaction kettle, adding a polythiophene aqueous solution with the mass of 0.5-20% of that of the solvent in a stirring state, adding zinc powder according to 10-70% of that of the solvent, heating to 20-50 ℃, and reacting for 0.5-3 h; centrifuging the reactant, taking out the powder, rinsing the powder for 2-5 times by using a solvent, drying the powder for 10-24 hours at the temperature of 40-70 ℃, and grinding the powder into powder to prepare modified zinc powder;
(2) adding acrylic resin, a solvent and an auxiliary agent into a reaction kettle in sequence, and dispersing for 15-50 min at the rotating speed of 300-1000 rpm; then slowly adding the modified zinc powder, dispersing for 30-100 min at 300-1000 rpm, filtering and discharging to prepare the polythiophene modified cold-coating zinc coating.
The present invention will be described in further detail below with reference to comparative examples and examples. In the following examples, the content of the sodium polystyrene sulfonate-doped poly (3, 4-ethylenedioxythiophene) in the aqueous solution of the sodium polystyrene sulfonate-doped poly (3, 4-ethylenedioxythiophene) was 1.5 wt%, and the doping amount of the sodium polystyrene sulfonate was 160 wt% of the poly (3, 4-ethylenedioxythiophene).
Example 1
In the embodiment, deionized water is added into a reaction kettle, 1% of sodium polystyrene sulfonate doped poly (3, 4-ethylenedioxythiophene) water solution by mass of the deionized water is added in a stirring state, zinc powder is added according to 40% of the mass of the deionized water, and the mixture is heated to 30 ℃ to react for 1 hour; centrifuging the reactant, taking out the powder, rinsing the powder for 3 times by using deionized water, drying the powder for 15 hours at the temperature of 60 ℃, and then grinding the powder into powder to prepare modified zinc powder;
adding 166.7kg of acrylic resin, 200kg of toluene, 0.4kg of Disperbyk-140 dispersing agent, 0.5kg of BYK-055 defoaming agent, 0.4kg of EFKA 3600N leveling agent and 0.4kg of BENTONE 52 anti-settling agent into a reaction kettle in sequence, and dispersing for 20min at the rotating speed of 700 rpm; then 833.3kg of modified zinc powder is slowly added, dispersed for 70min at 1200rpm, and discharged after filtration, thus preparing the sodium polystyrene sulfonate doped poly (3, 4-ethylenedioxythiophene) modified cold galvanizing coating.
Example 2
In the embodiment, deionized water is added into a reaction kettle, 8% of polystyrene sodium sulfonate doped poly (3, 4-ethylenedioxythiophene) water solution by mass of the deionized water is added in a stirring state, zinc powder is added according to 40% of the mass of the deionized water, and the mixture is heated to 30 ℃ to react for 1 hour; centrifuging the reactant, taking out the powder, rinsing the powder for 3 times by using deionized water, drying the powder for 15 hours at the temperature of 60 ℃, and then grinding the powder into powder to prepare modified zinc powder;
adding 166.7kg of acrylic resin, 200kg of toluene, 0.4kg of Disperbyk-140 dispersing agent, 0.5kg of BYK-055 defoaming agent, 0.4kg of EFKA 3600N leveling agent and 0.4kg of BENTONE 52 anti-settling agent into a reaction kettle in sequence, and dispersing for 20min at the rotating speed of 700 rpm; then 833.3kg of modified zinc powder is slowly added, dispersed for 70min at 1200rpm, and discharged after filtration, thus preparing the sodium polystyrene sulfonate doped poly (3, 4-ethylenedioxythiophene) cold galvanizing coating.
Example 3
In the embodiment, deionized water is added into a reaction kettle, polystyrene sodium sulfonate doped poly (3, 4-ethylenedioxythiophene) water solution with the mass of 15% of that of the deionized water is added in a stirring state, zinc powder is added according to 40% of that of the deionized water, and the mixture is heated to 30 ℃ to react for 1 hour; centrifuging the reactant, taking out the powder, rinsing the powder for 3 times by using deionized water, drying the powder for 15 hours at the temperature of 60 ℃, and then grinding the powder into powder to prepare modified zinc powder;
adding 166.7kg of acrylic resin, 200kg of toluene, 0.4kg of Disperbyk-140 dispersing agent, 0.5kg of BYK-055 defoaming agent, 0.4kg of EFKA 3600N leveling agent and 0.4kg of BENTONE 52 anti-settling agent into a reaction kettle in sequence, and dispersing for 20min at the rotating speed of 700 rpm; then 833.3kg of modified zinc powder is slowly added, dispersed for 70min at 1200rpm, and discharged after filtration, thus preparing the sodium polystyrene sulfonate doped poly (3, 4-ethylenedioxythiophene) cold galvanizing coating.
Comparative example 1
In the comparative example, 166.7kg of acrylic resin, 200kg of toluene, 0.4kg of Disperbyk-140 dispersing agent, 0.5kg of BYK-055 defoaming agent, 0.4kg of EFKA 3600N leveling agent and 0.4kg of BENTONE 52 anti-settling agent are sequentially added into a reaction kettle and dispersed for 20min at the rotating speed of 700 rpm; then 833.3kg of zinc powder without modification treatment is slowly added, dispersed for 70min at 1200rpm, and discharged after filtration, thus preparing the cold galvanizing coating.
And (3) testing the performance of the cold galvanizing coating:
testing of corrosion potential: the test was performed using a Princeton 273A electrochemical test system. The electrolytic cell adopts a three-electrode system, the auxiliary electrode is a platinum electrode, the reference electrode is a Saturated Calomel Electrode (SCE), the coating/matrix sample is a working electrode, and the effective area of the working electrode is about 12.56cm2The corrosion medium is 3.5 wt% NaCl solution, and the corresponding soaking time when the corrosion potential is-0.86V/SCE is recorded, namely the time is equivalent to the cathodic protection action time of the coating.
TABLE 1 coating test results
| Soaking time h corresponding to corrosion potential of-0.86V | |
| Comparative example 1 | 2000 |
| Example 1 | 2400 |
| Example 2 | 2550 |
| Example 3 | 2680 |
Table 1 shows the results of the coating tests. From the test results obtained, it can be seen that the cathodic protection times of the coatings prepared in examples 1, 2 and 3 are extended by 20%, 27.5% and 34%, respectively, with reference to comparative example 1, after the zinc powder has been modified with an aqueous solution of sodium polystyrene sulfonate-doped poly (3, 4-ethylenedioxythiophene). The method for modifying the polythiophene aqueous solution can enhance the cathode protection effect of the coating and improve the corrosion protection performance of the coating.
Claims (1)
1. The polythiophene modified cold-coating zinc coating is characterized by comprising the following components in parts by weight:
2-30 parts of acrylic resin;
0.1-6 parts of an auxiliary agent;
70-98 parts of zinc powder;
2-60 parts of a solvent;
the preparation method of the polythiophene modified cold-coating zinc coating comprises the following steps:
(1) adding a solvent into a reaction kettle, adding a sodium polystyrene sulfonate-doped poly (3, 4-ethylenedioxythiophene) aqueous solution accounting for 0.5-20% of the mass of the solvent under stirring, adding zinc powder accounting for 10-70% of the mass of the solvent, heating to 20-50 ℃, and reacting for 0.5-3 h; centrifuging the reactant, taking out the powder, rinsing the powder for 2-5 times by using a solvent, drying the powder for 10-24 hours at the temperature of 40-70 ℃, and grinding the powder into powder to prepare modified zinc powder;
(2) adding acrylic resin, a solvent and an auxiliary agent into a reaction kettle in sequence, and dispersing for 15-50 min at the rotating speed of 300-1000 rpm; then adding modified zinc powder, dispersing at 300-1000 rpm for 30-100 min, filtering and discharging to prepare polythiophene modified cold-coating zinc coating;
the zinc powder is modified by poly (3, 4-ethylenedioxythiophene) water solution doped with sodium polystyrene sulfonate, the content of the poly (3, 4-ethylenedioxythiophene) doped with the sodium polystyrene sulfonate in the poly (3, 4-ethylenedioxythiophene) water solution doped with the sodium polystyrene sulfonate is 0.3-20 wt%, and the doping amount of the sodium polystyrene sulfonate is 100-2500 wt% of the poly (3, 4-ethylenedioxythiophene).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201910533478.3A CN110317478B (en) | 2019-06-19 | 2019-06-19 | A kind of polythiophene modified cold coating zinc coating and preparation method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201910533478.3A CN110317478B (en) | 2019-06-19 | 2019-06-19 | A kind of polythiophene modified cold coating zinc coating and preparation method thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN110317478A CN110317478A (en) | 2019-10-11 |
| CN110317478B true CN110317478B (en) | 2021-07-23 |
Family
ID=68119873
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201910533478.3A Active CN110317478B (en) | 2019-06-19 | 2019-06-19 | A kind of polythiophene modified cold coating zinc coating and preparation method thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN110317478B (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN112521790A (en) * | 2020-11-25 | 2021-03-19 | 武汉双虎涂料有限公司 | Modified zinc powder and preparation method and application thereof |
| KR20230118847A (en) * | 2020-12-15 | 2023-08-14 | 썬 케미칼 코포레이션 | Zinc Pigments for Waterborne Erosion Coatings |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5976419A (en) * | 1998-06-09 | 1999-11-02 | Geotech Chemical Company | Method for applying a coating that acts as an electrolytic barrier and a cathodic corrosion prevention system |
| JP2012500865A (en) * | 2008-08-21 | 2012-01-12 | イノーバ ダイナミクス インコーポレイテッド | Enhanced surfaces, coatings, and related methods |
| CN104449141B (en) * | 2014-12-04 | 2017-07-18 | 海南电力技术研究院 | Nano combined cold galvanizing coating and preparation method thereof |
| US10763512B2 (en) * | 2015-08-28 | 2020-09-01 | Toyota Motor Engineering & Manufacturing North America, Inc. | Lithium deposition with multilayer nanomebrane |
| CN105462435A (en) * | 2015-12-11 | 2016-04-06 | 中国石油天然气集团公司 | Conductive macromolecule modified waterborne epoxy zinc-rich primer and preparation method thereof |
| CN107236437B (en) * | 2017-06-13 | 2019-07-09 | 石家庄铁道大学 | A kind of water-based anti-corrosion coating and preparation method thereof |
-
2019
- 2019-06-19 CN CN201910533478.3A patent/CN110317478B/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| CN110317478A (en) | 2019-10-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN104449141B (en) | Nano combined cold galvanizing coating and preparation method thereof | |
| CN110317478B (en) | A kind of polythiophene modified cold coating zinc coating and preparation method thereof | |
| CN105400373A (en) | Graphene/deimpurity polyaniline-containing anticorrosive coating and preparation method thereof | |
| CN106832183A (en) | A kind of Graphene modified cathode polyurethane electrophoresis resin and its cataphoresis paint composition | |
| CN103555137A (en) | Doped polyaniline-epoxy-zinc powder composite coating and preparation method thereof | |
| CN116970295B (en) | A "brick-mud" layered structure corrosion-resistant phosphate composite coating and its preparation method and application | |
| CN102786873B (en) | Nano compound anticorrosive paint and preparation method thereof | |
| CN102977730A (en) | Metal antirust paint treating modified attapulgite as filler, and its preparation method | |
| CN109593439B (en) | Modified graphene oxide water-based epoxy zinc-rich primer and preparation method thereof | |
| CN115044291A (en) | Anticorrosive grounding material and processing technology thereof | |
| CN112592652A (en) | Preparation method of polyaniline/cerium nitrate/epoxy polymer coating | |
| CN111974655A (en) | Preparation method of neodymium iron boron magnet with corrosion resistance | |
| CN110982373A (en) | Water-based heavy-duty anti-corrosion flame-retardant coating for metal substrate and preparation method thereof | |
| CN102977664A (en) | Metal antirust paint treating modified diatomite as filler, and its preparation method | |
| CN101591493A (en) | A kind of surface coating composition and preparation method thereof | |
| CN110093088B (en) | Graphene-like self-dispersing coating and preparation method thereof | |
| CN116656222B (en) | A method for preparing environmentally friendly and highly weather-resistant water-based automotive topcoat | |
| CN118027784B (en) | Magnesium alloy primer and preparation method thereof | |
| CN102964992A (en) | Coating scheme of anti-corrosion coating | |
| CN109486356B (en) | Epoxy static-conductive corrosion-resistant finish paint and preparation method thereof | |
| CN116948448A (en) | Self-repairing hydrotalcite-based nano material, composite coating and preparation method thereof | |
| CN119242145A (en) | Water-based zinc-aluminum anticorrosive paint and preparation method thereof | |
| CN115029027A (en) | Graphene zinc-loaded powder and anticorrosive coating based on same | |
| CN115029026A (en) | Graphene anti-corrosion coating for magnesium alloy and preparation method thereof | |
| CN113026071A (en) | Preparation method and application of conductive polymer and hexadecyl trimethyl ammonium bromide composite coating |
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 |