CN106009934A - Resin color paste and production process thereof - Google Patents
Resin color paste and production process thereof Download PDFInfo
- Publication number
- CN106009934A CN106009934A CN201610344718.1A CN201610344718A CN106009934A CN 106009934 A CN106009934 A CN 106009934A CN 201610344718 A CN201610344718 A CN 201610344718A CN 106009934 A CN106009934 A CN 106009934A
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- parts
- resin
- epoxy
- epoxy resin
- mill base
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Classifications
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- 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
- C09D17/00—Pigment pastes, e.g. for mixing in paints
- C09D17/002—Pigment pastes, e.g. for mixing in paints in organic medium
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Epoxy Resins (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Paints Or Removers (AREA)
Abstract
The invention discloses resin color paste and a production process thereof, and belongs to the technical field of anticorrosive paint. The resin color paste is prepared by performing chemical reaction and mixing on 260 to 330 parts of epoxy resin, 130 to 160 parts of ether alcohol solvents, 60 to 80 parts of isooctanol, 35 to 50 parts of diethanolameineb and 100 to 200 parts of polyamine resin and dispersing the obtained material in 10 to 20 parts of de-ionized water through being metered in parts by weight. The production process comprises epoxy resin melting, raw material addition and heat insulation reaction. In the resin color paste production process, the loss is little; the production cost is reduced; the hole shrinkage resistance effect is good; the product quality is improved; the hydrophilicity is high. Through the production process, the ring opening of epoxy resin is proper; the raw material waste is avoided; meanwhile, the water solubility of the epoxy resin is improved; the hole shrinkage of products is eliminated; the product quality is improved.
Description
Technical field
The present invention relates to anticorrosive paint technical field, specifically a kind of resin mill base and production technology thereof.
Background technology
Resin mill base is that to produce coating be one of the raw material used, for producing the resin mill base of water paint, it is desirable to its water solublity
Must get well, otherwise, after coating mixes with water, mill base can float in water, can cause pigment coloration poor effect;Additionally,
In resin mill base production process, it is easy to shrinkage cavity can be produced, produce shrinkage cavity and can cause the decline of product quality, also result in the later stage
When coating uses, paint film is unsmooth;Furthermore, during resin mill base produces, need heating and insulation, so that each raw material
Between reaction can be normally carried out, but heating and insulation during, solvent is readily volatilized, causes raw materials for production
Waste and the pollution of environment, bring loss and inconvenience to manufacturing enterprise.
Summary of the invention
For above-mentioned the deficiencies in the prior art, it is an object of the invention to provide a kind of resin mill base and production technology thereof, to solve
The problems referred to above.
The present invention solves the technical scheme that its technical problem taked and includes: a kind of resin mill base, including 260~330 parts of asphalt mixtures modified by epoxy resin
Fat, 130~160 parts of alcohol ether solvents, 60~80 parts of isooctanol, 35~50 parts of diethanolamine and polyimide resin more than 100~200 parts,
After chemical reaction and mixing, disperse to make in 10~20 parts of deionized waters, and above number is by weight.
The boils up till of isooctanol 185-189 DEG C, compares other solvents, and boiling point is high.Production at resin mill base
Cheng Zhong, reaction temperature is typically at about 100 DEG C.Select isooctanol as solvent, utilize the feature that its boiling point is high, producing
In journey the most volatile, both reduced loss, again safety and environmental protection;Meanwhile, isooctanol also has antiseptical effect, increases coating
Antiseptic effect.
In order to further increase the water solublity of epoxy resin, further technical scheme is: also include 1~3 part of ethylenediamine, should
Number is by weight.
Further technical scheme is: also including 200~300 parts of cross-linking agent, this number is by weight.Each raw material in production process
Disperseing bad to produce shrinkage cavity in water, cross-linking agent can play nonshrink hole effect, it is to avoid produces shrinkage cavity, improves the product of product
Matter.
Further technical scheme is: described alcohol ether solvents is propylene glycol monomethyl ether.Propylene glycol monomethyl ether can strengthen thickness.Do not add
Entering the film thickness of propylene glycol monomethyl ether generally about 10 μm, antiseptic effect is poor;After adding propylene glycol monomethyl ether, paint film thickness
Degree is up to 20-30 μm, and antiseptic property is greatly improved.Additionally, propylene glycol monomethyl ether is low to the toxicity of human body, safer.
Further technical scheme is: described cross-linking agent is made up according to weight proportion of the raw material of following component: more than 280~340 parts
Isocyanates, 140~180 parts of butyl glycol ethers, 200~250 parts of isooctanol, 1~4 part of catalyst and 280~320 parts the third two
Alcohol methyl ether.
Further technical scheme is: described polyisocyanates is TDI, and described catalyst is organic tin liquor.TDI is that toluene two is different
Cyanate, is that a kind of sealer, TDI and diethanolamine coordinate, epoxy resin not open loop can either be avoided to cause it not have water
The problem of dissolubility, again it can be avoided that epoxy resin open loop causes its water solublity too strong too much, so that the problem that solvent loss is the biggest,
Achieve the moderate of epoxy resin open loop, it is ensured that while product quality, reduce the loss of raw material, reduce production cost.
The present invention solves the scheme of its technical problem and also includes: the production technology of a kind of resin mill base, comprises the following steps:
Step 1: 60~80 parts of isooctanol and 130~160 parts of propylene glycol monomethyl ethers are added in the change epoxy still of melting ring epoxy resins,
Then in changing epoxy still, add 260~330 parts of epoxy resin;
Step 2: change the internal intensification of epoxy still, until epoxy resin all melts;
Step 3: the epoxy resin after fusing is put into reactor, heats up and start stirring, add 35~50 parts in reactor
Diethanolamine and 1~3 part of ethylenediamine, reaction is to epoxy resin open loop;
Step 4: add polyimide resin more than 100~200 parts and 200~300 parts of cross-linking agent to reactor, is tamping anti-after charging
Answer the kettle cover of still;
Step 5: be warming up to 110 DEG C ± 2 DEG C, insulation reaction more than 2 hours, be then cooled to less than 100 DEG C, add 10~
20 parts of deionized waters, and insulation reaction 1~1.5 hours at this temperature, preparation completes;
In above-mentioned steps, the number of each raw material is by weight.
Further technical scheme is: in step 3, be warming up to when 80 DEG C add described diethanolamine and described ethylenediamine, insulation
React more than 2 hours.The ring that insulation can make epoxy resin in more than two hours is opened, if temperature retention time is the shortest, then and epoxy resin
Ring do not open, epoxy resin does not have water solublity.
Further technical scheme is: in step 4, after adding described many polyimide resins, be warming up to 100 DEG C ± 2 DEG C, and insulation 2 is little
Described cross-linking agent is added time after.
Further technical scheme is: in production process, the condenser of reactor is passed through cooling water, described epoxy melting after,
The agitating device of described reactor starts stirring and stirs to having prepared.
In step 5, after being warming up to 110 DEG C ± 2 DEG C, temperature retention time must be more than 2 hours, if temperature retention time is held not
It is easily generated shrinkage cavity.
The invention has the beneficial effects as follows:
1, isooctanol boils up till 185-189 DEG C, compares other solvents, and boiling point is high.Production at resin mill base
Cheng Zhong, reaction temperature is typically at about 100 DEG C.Select isooctanol as solvent, utilize the feature that its boiling point is high, producing
In journey the most volatile, both reduced loss, again safety and environmental protection;Meanwhile, isooctanol also has antiseptical effect, increases coating
Antiseptic effect.
2, adding diethanolamine and can increase the water solublity of epoxy resin, product hydrophilic is more preferable, does not haves layering after adding water
Phenomenon, the coloring effect of coating is more preferable, and product quality is finer and smoother.
3, add cross-linking agent and there is the effect in nonshrink hole, it is to avoid shrinkage cavity occurs in product, and paint film is more smooth.
4, cross-linking agent adds TDI as sealer, it is possible to avoid epoxy resin open loop to cause its water solublity too strong too much, thus
Make the problem that solvent loss is the biggest, it is achieved that epoxy resin open loop moderate, it is ensured that while product quality, reduce the loss of raw material,
Reduce production cost.
5, the production technology of the present invention, the order of addition of rational arranging raw material, reaction temperature and response time, production efficiency is high,
Ensure that epoxy resin open loop is moderate, make product water dissolubility moderate, and avoid product to produce shrinkage cavity, improving product in process of production
Quality.
6, the production technology of the present invention, the part of exothermic reaction uses dropping mode to feed, it is to avoid solvent boiling phenomenon occurs, protects
The waste of solvent is avoided in card reaction while being normally carried out.
Detailed description of the invention
Below in conjunction with specific embodiment, the invention will be further described:
Embodiment one:
A kind of resin mill base, is made up of following raw material:
Production technology comprises the following steps:
Step 1: by the isooctanol of formula ratio and the change epoxy still of propylene glycol monomethyl ether addition melting ring epoxy resins, be subsequently adding and join
The CYD epoxy resin of side's amount, the condenser changed on epoxy still and reactor is passed through cooling water.
Step 2: temperature rises to insulation when 80 DEG C, after the epoxy resin in changing epoxy still all melts, opens kettle cover, observes
Confirm all fusings.
Step 3: the epoxy resin after fusing is put into reactor, when temperature of reaction kettle rises to 80 DEG C, starts stirring, adds second
Diamidogen and diethanolamine, be incubated 2 hours.
Step 4: after insulation terminates, add many polyimide resins, be warming up to 100 DEG C, add cross-linking agent after being incubated 2 hours, charging
After be tamping the kettle cover of reactor.
Step 5: be warming up to 110 DEG C, insulation reaction 2 hours, then it is cooled to 80 DEG C, adds the deionized water of formula ratio,
And insulation reaction 1 hour at this temperature, discharging is standby, and personnel of controlling in notice sample detection.
Embodiment two:
A kind of resin mill base, is made up of following raw material:
Production technology comprises the following steps:
Step 1: by the isooctanol of formula ratio and the change epoxy still of propylene glycol monomethyl ether addition melting ring epoxy resins, be subsequently adding and join
The CYD epoxy resin of side's amount, the condenser changed on epoxy still and reactor is passed through cooling water.
Step 2: temperature rises to insulation when 85 DEG C, after the epoxy resin in changing epoxy still all melts, opens kettle cover, observes
Confirm all fusings.
Step 3: the epoxy resin after fusing is put into reactor, when temperature of reaction kettle rises to 85 DEG C, starts stirring, adds second
Diamidogen and diethanolamine, be incubated 2.5 hours.
Step 4: after insulation terminates, add many polyimide resins, be warming up to 102 DEG C, add cross-linking agent after being incubated 2.5 hours, add
The kettle cover of reactor it is tamping after material.
Step 5: be warming up to 112 DEG C, insulation reaction 2.5 hours, then it is cooled to 90 DEG C, adds the deionization of formula ratio
Water, and insulation reaction 1.5 hours at this temperature, discharging is standby, and personnel of controlling in notice sample detection.
Embodiment three:
A kind of resin mill base, is made up of following raw material:
Production technology comprises the following steps:
Step 1: by the isooctanol of formula ratio and the change epoxy still of propylene glycol monomethyl ether addition melting ring epoxy resins, be subsequently adding and join
The CYD epoxy resin of side's amount, the condenser changed on epoxy still and reactor is passed through cooling water.
Step 2: temperature rises to insulation when 82 DEG C, after the epoxy resin in question response still all melts, opens kettle cover, observes really
Recognize all fusings.
Step 3: the epoxy resin after fusing is put into reactor, when temperature of reaction kettle rises to 83 DEG C, starts stirring, adds second
Diamidogen and diethanolamine, be incubated 2.2 hours.
Step 4: after insulation terminates, add many polyimide resins, be warming up to 98 DEG C, add cross-linking agent after being incubated 2.2 hours, add
The kettle cover of reactor it is tamping after material.
Step 5: be warming up to 108 DEG C, insulation reaction 2.2 hours, then it is cooled to 85 DEG C, adds the deionization of formula ratio
Water, and insulation reaction 1.2 hours at this temperature, discharging is standby, and personnel of controlling in notice sample detection.
In above-described embodiment, cross-linking agent is made up according to weight proportion of the raw material of following component:
The production technology of above-mentioned cross-linking agent comprises the following steps:
Step 1: checking that reactor is the cleanest, whether each pipeline, valve put in place.
Step 2: with the TDI of vacuum suction formula ratio, the condenser on reactor is passed through cooling water, opens stirring and adds formula ratio
Organic tin liquor.
Step 3: when temperature of charge rises to 60 DEG C, starts to drip the isooctanol pumping in measuring tank in advance, after dropping,
Drip butyl glycol ether again.This reaction is exothermic reaction, notes variations in temperature, controls rate of addition, and controls temperature at 60-65 DEG C
Between, the rate of addition of isooctanol and butyl glycol ether is at about 350 kgs/hour.
Step 4: after dropping, 70-75 DEG C of insulation reaction 2 hours, then heats to 88-92 DEG C, and insulation reaction 2 is little
Time, insulation is down to 80 DEG C and is added propylene glycol monomethyl ether after terminating, in the hermetic container that after stirring, discharging is the cleanest, dry, and
Personnel of controlling in notice survey solid content, stand-by.
The foregoing is only presently preferred embodiments of the present invention, be not whole embodiments of the present invention, not in order to limit this
Bright, all within the spirit and principles in the present invention, any modification, equivalent substitution and improvement etc. made, should be included in this
Within bright protection domain.
In addition to technical characteristic described in description, remaining technical characteristic is all known to a person skilled in the art technology, in order to highlight this
Bright innovative characteristics, above-mentioned technical characteristic does not repeats them here.
Claims (10)
1. a resin mill base, is characterized in that, including 260~330 parts of epoxy resin, 130~160 parts of alcohol ether solvents, 60~
80 parts of isooctanol, 35~50 parts of diethanolamine and polyimide resin, after chemical reaction and mixing more than 100~200 parts, 10~20
Disperseing to make in part deionized water, above number is by weight.
A kind of resin mill base the most according to claim 1, is characterized in that, also include 1~3 part of ethylenediamine, this number with
Weight meter.
A kind of resin mill base the most according to claim 1 and 2, is characterized in that, also include 200~300 parts of cross-linking agent,
This number is by weight.
A kind of resin mill base the most according to claim 1, is characterized in that, described alcohol ether solvents is propylene glycol monomethyl ether.
A kind of resin mill base the most according to claim 3, is characterized in that, described cross-linking agent by the raw material of following component according to
Weight proportion is made: 280~340 parts of polyisocyanates, 140~180 parts of butyl glycol ethers, 200~250 parts of isooctanol, 1~
4 parts of catalyst and 280~320 parts of propylene glycol monomethyl ethers.
A kind of resin mill base the most according to claim 5, is characterized in that, described polyisocyanates is TDI, described catalysis
Agent is organic tin liquor.
7. a production technology for resin mill base, is characterized in that, comprises the following steps:
Step 1: 60~80 parts of isooctanol and 130~160 parts of propylene glycol monomethyl ethers are added in the change epoxy still of melting ring epoxy resins,
Then in changing epoxy still, add 260~330 parts of epoxy resin;
Step 2: change the internal intensification of epoxy still, until epoxy resin all melts;
Step 3: the epoxy resin after fusing is put into reactor, heats up and start stirring, add 35~50 parts in reactor
Diethanolamine and 1~3 part of ethylenediamine, reaction is to epoxy resin open loop;
Step 4: add polyimide resin more than 100~200 parts and 200~300 parts of cross-linking agent to reactor, is tamping anti-after charging
Answer the kettle cover of still;
Step 5: be warming up to 110 DEG C ± 2 DEG C, insulation reaction more than 2 hours, be then cooled to less than 100 DEG C, add 10~
20 parts of deionized waters, and insulation reaction 1~1.5 hours at this temperature, preparation completes;
In above-mentioned steps, the number of each raw material is by weight.
Production technology the most according to claim 7, is characterized in that, in step 3, is warming up to when 80 DEG C add described two
Ethanolamine and described ethylenediamine, insulation reaction more than 2 hours.
Production technology the most according to claim 7, is characterized in that, in step 4, after adding described many polyimide resins, heats up
To 100 DEG C ± 2 DEG C, after being incubated 2 hours, add described cross-linking agent.
Production technology the most according to claim 7, is characterized in that, in production process, the condenser of reactor is passed through cooling
Water, described epoxy melting after, the agitating device of described reactor starts stirring and stirs to having prepared.
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108373661A (en) * | 2017-06-08 | 2018-08-07 | 江西乔威化工有限公司 | A kind of production technology of water paint mill base |
CN115558382A (en) * | 2022-10-19 | 2023-01-03 | 山东优固德环保科技有限公司 | Simple and rapid construction floor paint and preparation method thereof |
CN115717029A (en) * | 2022-12-08 | 2023-02-28 | 上海正欧实业有限公司 | Low-temperature curing epoxy floor paint and preparation method thereof |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1122353A (en) * | 1994-11-02 | 1996-05-15 | 化学工业部常州涂料化工研究院 | Resin used for cathode electrodeposition paint and its production and application |
CN1231316A (en) * | 1998-04-09 | 1999-10-13 | 化工部常州涂料化工研究院 | Preparation of resin emulsion for electrophoretic paint used on thick-film cathode |
CN103146295A (en) * | 2013-03-01 | 2013-06-12 | 广东科德化工实业有限公司 | Matte cathode electrophoresis coating as well as preparation method and use method for same |
CN103965740A (en) * | 2014-05-20 | 2014-08-06 | 广东科德化工实业有限公司 | Sand finish type cathode electrophoretic coating and preparation method thereof |
-
2016
- 2016-05-23 CN CN201610344718.1A patent/CN106009934B/en active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1122353A (en) * | 1994-11-02 | 1996-05-15 | 化学工业部常州涂料化工研究院 | Resin used for cathode electrodeposition paint and its production and application |
CN1231316A (en) * | 1998-04-09 | 1999-10-13 | 化工部常州涂料化工研究院 | Preparation of resin emulsion for electrophoretic paint used on thick-film cathode |
CN103146295A (en) * | 2013-03-01 | 2013-06-12 | 广东科德化工实业有限公司 | Matte cathode electrophoresis coating as well as preparation method and use method for same |
CN103965740A (en) * | 2014-05-20 | 2014-08-06 | 广东科德化工实业有限公司 | Sand finish type cathode electrophoretic coating and preparation method thereof |
Non-Patent Citations (1)
Title |
---|
陈治良: "《电泳涂装实用技术》", 30 September 2009, 上海科学技术出版社 * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108373661A (en) * | 2017-06-08 | 2018-08-07 | 江西乔威化工有限公司 | A kind of production technology of water paint mill base |
CN115558382A (en) * | 2022-10-19 | 2023-01-03 | 山东优固德环保科技有限公司 | Simple and rapid construction floor paint and preparation method thereof |
CN115717029A (en) * | 2022-12-08 | 2023-02-28 | 上海正欧实业有限公司 | Low-temperature curing epoxy floor paint and preparation method thereof |
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