CN1380359A - Water polyurethane surface treating agent and its preparation method - Google Patents
Water polyurethane surface treating agent and its preparation method Download PDFInfo
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- CN1380359A CN1380359A CN 01110616 CN01110616A CN1380359A CN 1380359 A CN1380359 A CN 1380359A CN 01110616 CN01110616 CN 01110616 CN 01110616 A CN01110616 A CN 01110616A CN 1380359 A CN1380359 A CN 1380359A
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Abstract
The present invention relates to a water-soluble polyurethane surface treatment agent and its preparation method. Said preparation method includes the following steps: placing 30-60 portions of polyester polyol monomer, 30-60 portions of polyether or low polymer polyol monomer or 30-110 portions of their mixutre and 1-5 portions of nano-level inorganic material in a container, heated and vacuum-pumped, drop-adding 20-50 portions of isocyanate, and adding acetone solutions in which one solution contains 5-10 portions of hydrophilic chain extender and another solution contains 1-10 portions of triethanolamine and their percentage concentrations respectively are 10-20 % and 10-20% making reaction, stirring, adding distilled water, stirring, vacuum-pumping and removing actone so as to obtain the surface treatment agent.
Description
The invention belongs to macromolecule surface treatment agent field, specially refer to urethane and strengthen between the inorganic materials, and the water polyurethane surface treating agent between inorganic materials and the organic materials and preparation method thereof.
Glass fibre, inorganic materials fibers such as mineral wool are cheap because of it, have good weathering resistance and are used for manufacturing sound absorption, protection against the tide, heat insulation and damping board wall widely.But inorganic materials such as glass fibre, mineral wool fiber weakness is big, intensity is low, only depends on interlaced, winding effect between the fiber, and bulk strength is also difficult to be improved, and affected by environment in outdoor application, its bulk strength is lower.Especially in rainy season and high damp-heat air easily the adsorptive enzyme bacterium and mouldy, easily absorb large quantity of moisture and come off, thereby lost sound absorption, protection against the tide, the heat insulation and damping effect of these board walls.Because glass fibre, these defectives of inorganic materials fibers such as mineral wool itself are restricted its many aspects in actual applications.
The object of the present invention is to provide a kind of being coated on inorganic materials fiber, plastics or the Metal walls such as glass fibre, mineral wool, make that to have cementability between inorganic materials fibers such as glass fibre, mineral wool and plastics or the Metal wall strong, flexible moderate, the water polyurethane surface treating agent of hydrophobic and good weatherability, big in order to overcome inorganic materials fiber weaknesses such as glass fibre and mineral wool, intensity is low, and result of use is poor, the shortcoming that the life-span is short.
A further object of the present invention provides a kind of preparation method of water polyurethane surface treating agent.
Surface treatment agent of the present invention is to be the polyaminoester emulsion of dispersion agent with water, and is equipped with nano-grade inorganics, and the component and the content of its raw material are as follows, in parts by weight:
The monomeric mixture 30-110 of polyester polyols alcohol monomer 30-60 or polyethers or oligomer polyol monomer 30-60 or polyester polyols alcohol monomer and polyethers or oligomer polyol
Isocyanic ester 20-50
Wetting ability chainextender 5-10
Nano-grade inorganics 1-5
Triethylamine 1-10
Distilled water 300-400.
Polyester polyols alcohol monomer of the present invention is: the polyester polyol that is formed by di-carboxylic acid and dibasic alcohol dehydration polycondensation, poly--the 6-caprolactone glycol, poly-carbonic acid hexylene glycol esterdiol or their mixture etc.
Described di-carboxylic acid comprises hexanodioic acid, nonane diacid, sebacic acid, Succinic Acid, maleic acid, terephthalic acid etc.; Dibasic alcohol comprises ethylene glycol, 1, and 2-propylene glycol, 1,4-butyleneglycol, 1,6-hexylene glycol, second condensed ethandiol, dipropylene glycol, methyl propanediol, dihydroxyphenyl propane etc.
Described polyethers and oligomer polyol monomer are: polyoxypropyleneglycol, polytetrahydrofuran diol, polybutadiene diol, tetrahydrofuran (THF)-propylene oxide copolymerization glycol, polyoxytrimethylene triol, polyoxytrimethylene-castor oil polyhydric alcohol, Polybutadiene-acrylonitrile copolymerization glycol or their mixture etc.
Described isocyanic ester is: tolylene diisocyanate, ditan-4,4 '-vulcabond, hexamethylene diisocyanate, poly methylene poly phenyl poly isocyanate, xylylene diisocyanate, Methylcyclohexyl diisocyanate or dicyclohexyl methane diisocyanate etc.
Described wetting ability chainextender is: dimethylol propionic acid, dimethylolpropionic acid, dihydroxyl half ester, Ornithine or diaminobenzoic acid etc.
Described nano-grade inorganics is: zinc oxide, titanium dioxide, hydrotalcite or polynite etc.
The preparation method of water polyurethane surface treating agent of the present invention is as follows, in parts by weight:
With polyester polyols alcohol monomer 30-60 part, polyethers or oligomer polyol monomer 30-60 part or polyester polyols alcohol monomer and polyethers or the monomeric mixture 30-110 of oligomer polyol part, nano-grade inorganics places container for 1～5 part, heating 80-90 ℃ vacuumized about 30-60 minute, drip 20～50 parts of isocyanic ester at 50-60 ℃, drip and finish about 80～95 ℃ of stirring reaction 2-3 hours.When being cooled to 40-65 ℃, adding weight percent concentration and be the acetone soln that 10-20% contains 5～10 parts of wetting ability chainextenders and carry out chain extending reaction.Reaction under this temperature about 2-2.5 hour, be cooled to 40-50 ℃, add weight percent concentration and be the acetone soln that 10-20% contains 1～10 part of triethylamine and carry out neutralization reaction, in the stirring and about 30-60 minute, under high degree of agitation, slowly add 300～400 parts of distilled water, along with the adding of distilled water, reaction solution is by the faint yellow translucent white emulsion that becomes gradually.Stirred about 1 hour, and vacuumized and remove acetone, obtain the water polyurethane surface treating agent of pH=7-7.5.
Urethane provided by the present invention is water-tolerant not only, and chemically reactive height, be used for porous material surfaces such as glass fibre, mineral wool, timber, fabric, leather, realized ideal uniform dispersion and bonding interface, thereby reach the raising of the whole mechanical property of material product.
Urethane provided by the present invention has good snappiness, do the rear surface and form the extraordinary film of snappiness through urging with inorganic materials fibers such as the glass fibre of treated with same, mineral wools, this layer film is because snappiness is moderate, not only do not influence the starting material acoustically effective, but also can improve protection against the tide, heat insulation, the damping effect of inorganic materials fibers such as glass fibre, mineral wool.
The present invention mixes the nano grade inorganic oxide compound when the preparation base polyurethane prepolymer for use as, purpose is to utilize the surface effects of nano-grade inorganics, make this surface treatment agent have shielding ultraviolet rays and effect antibiotic, mildew-resistant, this function can prolong glass fibre effectively, inorganic materials fibers such as mineral wool are as sound absorption, the work-ing life of moistureproof, damping wallboard.
The present invention follows environmental regulation, adds the wetting ability chainextender when the preparation base polyurethane prepolymer for use as, to make water polyurethane surface treating agent; Because of being dispersion agent, do not have organic solvent again, do not fire so have with water, no stink, the VOC value is zero, advantages such as non-environmental-pollution easy-to-operate.
Below in conjunction with embodiment technical scheme of the present invention is further described.
Embodiment 1.
With polyoxypropyleneglycol 55g, Polybutadiene-acrylonitrile copolymerization glycol 45g, Nano titanium dioxide 5g places the 1000ml container, heat 80-90 ℃ vacuumize 30 minutes after, drip ditan-4 at 50-60 ℃, 4 '-vulcabond 45.5g drips and to finish 80-85 ℃ of stirring reaction 2 hours.When being cooled to 65 ℃, adding weight percent concentration is that 10% acetone soln that contains dimethylolpropionic acid 7.1g carries out chain extending reaction.Be cooled to 40 ℃ in reaction under this temperature after 2 hours, adding weight percent concentration is that 20% acetone soln that contains triethylamine 9g carries out neutralization reaction, in the stirring and after 30 minutes, under high degree of agitation, slowly add distilled water 370ml, along with the adding of distilled water, reaction solution is by the faint yellow translucent white emulsion that becomes gradually.Stir after 1 hour, vacuumize and remove acetone, get the translucent emulsion of little Huang (PU-01) of pH=7-7.5.
Embodiment 2.
With polyethylene glycol adipate glycol 60g, polytetrahydrofuran diol 40g, nano level zinc oxide 3g places the 1000ml container, heat 80-90 ℃ vacuumize 50 minutes after, drip tolylene diisocyanate 32.5g at 50-60 ℃, drip and finish 80-85 ℃ of stirring reaction 2.5 hours.When question response liquid was reduced to 60 ℃, adding weight percent concentration was that 15% acetone soln that contains dimethylol propionic acid 5.9g carries out chain extending reaction.Be cooled to 40 ℃ in reaction under this temperature after 2 hours, add weight percent concentration this moment is that 10% acetone soln that contains triethylamine 4.4g carries out neutralization reaction, in the stirring and after 30 minutes, under high degree of agitation, slowly add distilled water 330ml, this moment, reaction solution was bleached gradually by translucent liquid, became white emulsion at last.Stir after 1 hour, vacuumize and remove acetone, get the little bluish white emulsion (PU-02) of pH=7-7.5.
Embodiment 3.
With polyoxytrimethylene-castor oil polyhydric alcohol 30g, poly--6-caprolactone glycol 30g, poly-hexanodioic acid-1,4-butanediol ester glycol 40g, nano level hydrotalcite 4g places the 1000ml there-necked flask, heat 80-90 ℃ vacuumize 60 minutes after, drip toluene cyclohexyl diisocyanate 37.6g at 50-60 ℃, drip and finish 85-90 ℃ of stirring reaction 2 hours.When question response liquid was reduced to 40 ℃, adding weight percent concentration was that 20% acetone soln that contains Ornithine 7.8g carries out chain extending reaction.Be cooled to 40 ℃ in reaction under this temperature after 2 hours, add weight percent concentration this moment is that 20% acetone soln that contains triethylamine 5.4g carries out neutralization reaction, in the stirring and after 30 minutes, slowly add distilled water 350ml under high degree of agitation, this moment, reaction solution was bleached gradually by translucent.Stir after 1 hour, vacuumize and remove acetone, get the white emulsion (PU-03) of pH=7-7.5.
PU-01, PU-02, the performance test of PU-03 sees Table 1.
PU-01, PU-02, the performance test after the PU-03 film forming sees Table 2.
The performance test of table 1 surface treatment agent
Performance test after the table 2 surface treatment agent film forming
Claims (9)
1. water polyurethane surface treating agent is characterized in that: this treatment agent is to be the polyaminoester emulsion of dispersion agent with water, and is equipped with nano-grade inorganics, and the component and the content of its raw material are as follows, in parts by weight:
The monomeric mixture 30-110 of polyester polyols alcohol monomer 30-60 or polyethers or oligomer polyol monomer 30-60 or polyester polyols alcohol monomer and polyethers or oligomer polyol
Isocyanic ester 20-50
Wetting ability chainextender 5-10
Nano-grade inorganics 1-5
Triethylamine 1-10
Distilled water 300-400.
2. water polyurethane surface treating agent as claimed in claim 1 is characterized in that: described polyester polyols alcohol monomer is the polyester polyol that formed by di-carboxylic acid and dibasic alcohol dehydration polycondensation, poly--the 6-caprolactone glycol, poly-carbonic acid hexylene glycol esterdiol or their mixture.
3. water polyurethane surface treating agent as claimed in claim 2 is characterized in that: described di-carboxylic acid comprises hexanodioic acid, nonane diacid, sebacic acid, Succinic Acid, maleic acid, terephthalic acid.
4. water polyurethane surface treating agent as claimed in claim 2 is characterized in that: described dibasic alcohol comprises ethylene glycol, 1, and 2-propylene glycol, 1,4-butyleneglycol, 1,6-hexylene glycol, second condensed ethandiol, dipropylene glycol, methyl propanediol, dihydroxyphenyl propane.
5. water polyurethane surface treating agent as claimed in claim 1 is characterized in that: described polyethers and oligomer polyol monomer are: polyoxypropyleneglycol, polytetrahydrofuran diol, polybutadiene diol, tetrahydrofuran (THF)-propylene oxide copolymerization glycol, polyoxytrimethylene triol, polyoxytrimethylene-castor oil polyhydric alcohol, Polybutadiene-acrylonitrile copolymerization glycol or their mixture.
6. water polyurethane surface treating agent as claimed in claim 1, it is characterized in that: described isocyanic ester is tolylene diisocyanate, ditan-4,4 '-vulcabond, hexamethylene diisocyanate, poly methylene poly phenyl poly isocyanate, xylylene diisocyanate, Methylcyclohexyl diisocyanate or dicyclohexyl methane diisocyanate.
7. water polyurethane surface treating agent as claimed in claim 1 is characterized in that: described wetting ability chainextender is dimethylol propionic acid, dimethylolpropionic acid, dihydroxyl half ester, Ornithine or diaminobenzoic acid.
8. water polyurethane surface treating agent as claimed in claim 1 is characterized in that: described nano-grade inorganics is zinc oxide, titanium dioxide, hydrotalcite or polynite.
9. as the preparation method of the described water polyurethane surface treating agent of claim 1-8, it is characterized in that: in parts by weight:
With polyester polyols alcohol monomer 30-60 part, polyethers or oligomer polyol monomer 30-60 part or polyester polyols alcohol monomer and polyethers or the monomeric mixture 30-110 of oligomer polyol part, nano-grade inorganics places container for 1～5 part, heating 80-90 ℃ vacuumizes, drip 20～50 parts of isocyanic ester, stir, cooling adds weight percent concentration and is the acetone soln that 10-20% contains 5～10 parts of wetting ability chainextenders and carries out chain extending reaction; Add weight percent concentration and be the acetone soln that 10-20% contains 1～10 part of triethylamine and carry out neutralization reaction, stir, under high degree of agitation, slowly add 300～400 parts of distilled water, stir, vacuumize and remove acetone, obtain water polyurethane surface treating agent.
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| CNB011106166A CN1133699C (en) | 2001-04-11 | 2001-04-11 | Water polyurethane surface treating agent and its preparation method |
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Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101838457A (en) * | 2010-05-11 | 2010-09-22 | 陕西科技大学 | Preparation method of high-solid content crosslinking polyurethane aqueous dispersoid |
| CN102010497A (en) * | 2010-09-29 | 2011-04-13 | 上海汇得树脂有限公司 | Polyurethane resin as well as preparation method and application thereof |
| CN101597461B (en) * | 2009-07-10 | 2011-11-09 | 浙江东化实业有限公司 | Multiple curable aqueous hyperbranched polyurethane inorganic nanomaterial hybrid coating agent and preparation method thereof |
| CN101550224B (en) * | 2009-05-07 | 2012-01-11 | 四川大学 | Preparation method of cation polyurethane/inorganic nanometer material organic-inorganic hybrid coating agent |
| CN103468110A (en) * | 2013-09-23 | 2013-12-25 | 句容市睿远科技有限公司 | Polyurea waterproofing paint |
| CN105274850A (en) * | 2015-11-23 | 2016-01-27 | 辽宁恒星精细化工有限公司 | Waterborne high-moisture-permeability anti-ultraviolet functional coating glue and preparation method thereof |
| CN105294983A (en) * | 2015-10-16 | 2016-02-03 | 上海恒安聚氨酯股份有限公司 | Antibacterial thermoplastic polyurethane composite material and preparation method thereof |
| CN109134820A (en) * | 2018-06-22 | 2019-01-04 | 同济大学 | A kind of anion aqueous polyurethane nano-zinc oxide composite material and preparation method thereof |
| CN110770270A (en) * | 2017-06-22 | 2020-02-07 | 东洋高分子股份有限公司 | Aqueous polyurethane dispersion, process for producing aqueous polyurethane dispersion, aqueous coating composition, and coating film |
| CN110964171A (en) * | 2019-12-20 | 2020-04-07 | 万华化学集团股份有限公司 | Polyurethane polyurea water dispersion and preparation method and application thereof |
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2001
- 2001-04-11 CN CNB011106166A patent/CN1133699C/en not_active Expired - Fee Related
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101550224B (en) * | 2009-05-07 | 2012-01-11 | 四川大学 | Preparation method of cation polyurethane/inorganic nanometer material organic-inorganic hybrid coating agent |
| CN101597461B (en) * | 2009-07-10 | 2011-11-09 | 浙江东化实业有限公司 | Multiple curable aqueous hyperbranched polyurethane inorganic nanomaterial hybrid coating agent and preparation method thereof |
| CN101838457B (en) * | 2010-05-11 | 2011-12-28 | 陕西科技大学 | Preparation method of high-solid content crosslinking polyurethane aqueous dispersoid |
| CN101838457A (en) * | 2010-05-11 | 2010-09-22 | 陕西科技大学 | Preparation method of high-solid content crosslinking polyurethane aqueous dispersoid |
| CN102010497A (en) * | 2010-09-29 | 2011-04-13 | 上海汇得树脂有限公司 | Polyurethane resin as well as preparation method and application thereof |
| CN102010497B (en) * | 2010-09-29 | 2012-08-22 | 上海汇得化工有限公司 | Polyurethane resin as well as preparation method and application thereof |
| CN103468110A (en) * | 2013-09-23 | 2013-12-25 | 句容市睿远科技有限公司 | Polyurea waterproofing paint |
| CN103468110B (en) * | 2013-09-23 | 2016-01-27 | 句容市石狮冲压件厂 | A kind of waterproof paint |
| CN105294983A (en) * | 2015-10-16 | 2016-02-03 | 上海恒安聚氨酯股份有限公司 | Antibacterial thermoplastic polyurethane composite material and preparation method thereof |
| CN105274850A (en) * | 2015-11-23 | 2016-01-27 | 辽宁恒星精细化工有限公司 | Waterborne high-moisture-permeability anti-ultraviolet functional coating glue and preparation method thereof |
| CN110770270A (en) * | 2017-06-22 | 2020-02-07 | 东洋高分子股份有限公司 | Aqueous polyurethane dispersion, process for producing aqueous polyurethane dispersion, aqueous coating composition, and coating film |
| CN110770270B (en) * | 2017-06-22 | 2021-12-07 | 东洋高分子股份有限公司 | Aqueous polyurethane dispersion, process for producing aqueous polyurethane dispersion, aqueous coating composition, and coating film |
| CN109134820A (en) * | 2018-06-22 | 2019-01-04 | 同济大学 | A kind of anion aqueous polyurethane nano-zinc oxide composite material and preparation method thereof |
| CN109134820B (en) * | 2018-06-22 | 2021-03-26 | 同济大学 | Anionic waterborne polyurethane nano zinc oxide composite material and preparation method thereof |
| CN110964171A (en) * | 2019-12-20 | 2020-04-07 | 万华化学集团股份有限公司 | Polyurethane polyurea water dispersion and preparation method and application thereof |
| CN110964171B (en) * | 2019-12-20 | 2022-03-11 | 万华化学集团股份有限公司 | Polyurethane polyurea water dispersion and preparation method and application thereof |
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