CN103790021A - Production method for micro porous membrane fabric - Google Patents
Production method for micro porous membrane fabric Download PDFInfo
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- CN103790021A CN103790021A CN201210423405.7A CN201210423405A CN103790021A CN 103790021 A CN103790021 A CN 103790021A CN 201210423405 A CN201210423405 A CN 201210423405A CN 103790021 A CN103790021 A CN 103790021A
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- 239000004744 fabric Substances 0.000 title claims abstract description 83
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 19
- 239000012982 microporous membrane Substances 0.000 title abstract 3
- 229920005989 resin Polymers 0.000 claims abstract description 70
- 239000011347 resin Substances 0.000 claims abstract description 70
- 239000011248 coating agent Substances 0.000 claims abstract description 58
- 238000000576 coating method Methods 0.000 claims abstract description 58
- 238000005406 washing Methods 0.000 claims abstract description 57
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 43
- 238000001035 drying Methods 0.000 claims abstract description 40
- 229920003169 water-soluble polymer Polymers 0.000 claims abstract description 16
- 238000004513 sizing Methods 0.000 claims description 40
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical group [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 claims description 20
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 20
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 claims description 20
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 claims description 20
- 239000002270 dispersing agent Substances 0.000 claims description 19
- 238000004043 dyeing Methods 0.000 claims description 19
- 239000004677 Nylon Substances 0.000 claims description 16
- 229920001778 nylon Polymers 0.000 claims description 16
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 claims description 7
- 239000004354 Hydroxyethyl cellulose Substances 0.000 claims description 7
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 claims description 7
- 229920000742 Cotton Polymers 0.000 claims description 6
- 239000004368 Modified starch Substances 0.000 claims description 4
- 229920000881 Modified starch Polymers 0.000 claims description 4
- 239000002202 Polyethylene glycol Substances 0.000 claims description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 4
- 235000019426 modified starch Nutrition 0.000 claims description 4
- 229920001223 polyethylene glycol Polymers 0.000 claims description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 4
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 3
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 3
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 3
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 3
- 230000004888 barrier function Effects 0.000 claims description 2
- 235000019422 polyvinyl alcohol Nutrition 0.000 claims description 2
- 229920004934 Dacron® Polymers 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 8
- 229920002635 polyurethane Polymers 0.000 abstract description 7
- 239000004814 polyurethane Substances 0.000 abstract description 7
- 230000035699 permeability Effects 0.000 abstract description 5
- 239000012528 membrane Substances 0.000 abstract 3
- 238000007493 shaping process Methods 0.000 abstract 1
- 239000007788 liquid Substances 0.000 description 30
- 239000000203 mixture Substances 0.000 description 30
- 239000000047 product Substances 0.000 description 22
- 238000002360 preparation method Methods 0.000 description 19
- 239000003795 chemical substances by application Substances 0.000 description 16
- 239000013530 defoamer Substances 0.000 description 16
- 238000003756 stirring Methods 0.000 description 15
- 239000000843 powder Substances 0.000 description 14
- 238000005187 foaming Methods 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 4
- 238000004090 dissolution Methods 0.000 description 3
- 229920004933 Terylene® Polymers 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000003912 environmental pollution Methods 0.000 description 2
- 239000011268 mixed slurry Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- REZQBEBOWJAQKS-UHFFFAOYSA-N triacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO REZQBEBOWJAQKS-UHFFFAOYSA-N 0.000 description 2
- KAKVFSYQVNHFBS-UHFFFAOYSA-N (5-hydroxycyclopenten-1-yl)-phenylmethanone Chemical compound OC1CCC=C1C(=O)C1=CC=CC=C1 KAKVFSYQVNHFBS-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- RCEAADKTGXTDOA-UHFFFAOYSA-N OS(O)(=O)=O.CCCCCCCCCCCC[Na] Chemical compound OS(O)(=O)=O.CCCCCCCCCCCC[Na] RCEAADKTGXTDOA-UHFFFAOYSA-N 0.000 description 1
- 108010009736 Protein Hydrolysates Proteins 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000011527 polyurethane coating Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
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Abstract
The invention discloses a production method for micro porous membrane fabric. The production method comprises the steps of uniformly coating a mixed resin at least containing water dispersive polyurethane and a water-soluble polymer on a surface of a base cloth in a coating manner; drying to form a membrane; then washing the fabric with the formed membrane to dissolve the water-soluble polymer out from the membrane; and finally drying and shaping to obtain the micro porous membrane fabric. The production method is environment-friendly and simple in process. The obtained fabric has relatively high air permeability and moisture penetrability and soft handfeel, and is suitable for use in various outdoor sports wear.
Description
Technical field
The present invention relates to a kind of production method of micro-porous film fabric.
Background technology
Along with the raising of people's living standard, consumer has higher requirement to the comfortableness of garment material, motion, Waterproof Breathable field especially out of doors, and supply falls short of demand especially for demand in recent years.At present, on market, main product comprises two large classes: a class is micro-porous type waterproof moisture permeating fabric, and a class is anapsid waterproof moisture permeating fabric.
The method of producing at present micro-porous type waterproof moisture permeating fabric mainly comprises two large classes: a class is wet-process coating, its main principle is by exchange occurs forming micropore being dispersed in solvent type resin system the water in DMF and tank, although this method is applied often at present, but there is serious environmental pollution, the shortcoming such as production efficiency is low.Another kind of is intumescent coating, its main principle is that the form by resin being carried out to mechanical foaming forms micropore, at present this technology further method be: in prescription, add a certain amount of pore-foaming agent as mentioned in Chinese patent CN 102425069A, the micropore that by the mode of rubbing in water, mechanical foaming is formed after drying and forming-film is connected, but general all very large of the micropore that mechanical foaming obtains, and also heterogeneity very of size, so it is many that it generally applies in the production of leather, and the application in Waterproof Breathable field is relatively less out of doors.
Summary of the invention
The object of the present invention is to provide that a kind of production method is simple, the production method of environmental protection and the good micro-porous film fabric of moisture permeability.
The production method of micro-porous film fabric of the present invention, it comprises the steps:
1. the hybrid resin that at least contains water dispersant type polyaminoester and high molecular weight water soluble polymer is evenly coated to the surface of base cloth by the mode of coating, then drying and forming-film;
2. by washing, the high molecular weight water soluble polymer stripping in film is formed to microporous barrier again;
3. final drying sizing, obtains product.
Above-mentioned hybrid resin, is generally first high molecular weight water soluble polymer to be fully dissolved in water, is then thoroughly mixed to form with water dispersant type polyaminoester, can add as required a certain amount of bridging agent and defoamer in the time mixing.
Above-mentioned high molecular weight water soluble polymer is: sodium carboxymethylcellulose, polyethylene glycol, polyvinylpyrrolidone, polyvinyl alcohol, hydroxyethylcellulose, modified starch or shitosan.The high molecular weight water soluble polymer aqueous solution in use will take into full account the compatibility with water dispersant type polyaminoester, and stripping property when drying and forming-film after washing.High molecular weight water soluble polymer is preferably sodium carboxymethylcellulose and hydroxyethylcellulose.
The content of above-mentioned high molecular weight water soluble polymer is 5%~30%, and the number of content directly has influence on the quantity of micro-porous of formation and the impact that breathable moisture permeability is brought, and preferred content is 10%~20%.
The mode of above-mentioned washing can be cylinder washing or liquid-flow dyeing machine circulating water wash.The condition of washing is 50~90 ℃ of temperature, 20~60 minutes time.The dissolution rate 80~99.9% of high molecular polymer.Water temperature is too low or washing time is too short all can not make the abundant stripping of high molecular weight water soluble polymer, and water temperature over-high or washing time are long, easily cause the problem such as hydrolysis and cost increase of polyurethane resin.Washing condition is preferably 60~80 ℃ of temperature, 30~40 minutes time.
The present invention has no particular limits for the requirement of base cloth, can be terylene, nylon, cotton or polyester-cotton blend etc.But because coating needs the technique through washing after dry, may bring impact to a certain degree to the color of base cloth, so the base cloth preferably using is nylon fabrics.
By the production method of micro-porous film fabric of the present invention, thoroughly solve the problem that environmental pollution and production efficiency are low, the careful homogeneous of its micropore, moisture permeability can reach 10000g/m
224hr left and right
Accompanying drawing explanation
Fig. 1 is the high power lens electron microscope sectional drawing of embodiment 5.
Fig. 2 is the high power lens electron microscope sectional drawing of comparative example 2.
The specific embodiment
In the present invention, the method for testing of each performance is as follows:
(1) high molecular weight water soluble polymer dissolution rate (%)
Dissolution rate (%)=(the rear grammes per square metre of grammes per square metre-washing before washing)/high molecular weight water soluble polymer grammes per square metre.
(2) moisture permeability
JIS L 1099 A method standards.
Below in conjunction with embodiment and comparative example, the present invention is described in detail.
Embodiment 1
1. hybrid resin preparation, coating
First the sodium carboxymethylcellulose powder of 5g is dissolved in 120g water, after fully dissolving and 100g water dispersant type polyaminoester resin carry out abundant mix and blend, add 0.5g bridging agent and 0.5g defoamer simultaneously, after fully stirring, form coating mixed resin liquid, surface at nylon base cloth is evenly coated with above-mentioned mixed resin liquid by coating machine, then passes through continuous drying case (70 ℃-90 ℃-130 ℃-150 ℃) drying and forming-film;
2. washing
The washing condition of setting liquid-flow dyeing machine is 90 ℃ × 60 minutes, and above-mentioned one-tenth film fabric is dropped into wherein, fully washed, by the sodium carboxymethylcellulose stripping in film;
3. dry, sizing
Finally one-tenth film fabric is dried to (120 ℃ × 2 minutes), sizing (170 ℃ × 1 minute) processing, obtains product of the present invention, its performance is in table 1.
Embodiment 2
1. hybrid resin preparation, coating
First the sodium carboxymethylcellulose powder of 10g is dissolved in 120g water, after fully dissolving and 100g water dispersant type polyaminoester resin carry out abundant mix and blend, add 0.5g bridging agent and 0.5g defoamer simultaneously, after fully stirring, form coating mixed resin liquid, surface at nylon base cloth is evenly coated with above-mentioned mixed resin liquid by coating machine, then passes through continuous drying case (70 ℃-90 ℃-130 ℃-150 ℃) drying and forming-film;
2. washing
The washing condition of setting liquid-flow dyeing machine is 50 ℃ × 20 minutes, and above-mentioned one-tenth film fabric is dropped into wherein, fully washed, by the sodium carboxymethylcellulose stripping in film;
3. dry, sizing
Finally one-tenth film fabric is dried to (120 ℃ × 2 minutes), sizing (170 ℃ × 1 minute) processing, obtains product of the present invention, its performance is in table 1.
Embodiment 3
1. hybrid resin preparation, coating
With embodiment 2;
2. washing
The washing condition of setting liquid-flow dyeing machine is 70 ℃ × 40 minutes, and the one-tenth film fabric that 1. step is obtained drops into wherein, fully washing, by the sodium carboxymethylcellulose stripping in film;
3. dry, sizing
Finally one-tenth film fabric is dried to (120 ℃ × 2 minutes), sizing (170 ℃ × 1 minute) processing, obtains product of the present invention, its performance is in table 1.
Embodiment 4
1. hybrid resin preparation, coating
With embodiment 2;
2. washing
The washing condition of setting liquid-flow dyeing machine is 90 ℃ × 60 minutes, and the one-tenth film fabric that 1. step is obtained drops into wherein, fully washing, by the sodium carboxymethylcellulose stripping in film;
3. dry, sizing
Finally one-tenth film fabric is dried to (120 ℃ × 2 minutes), sizing (170 ℃ × 1 minute) processing, obtains product of the present invention, its performance is in table 1.
Embodiment 5
1. hybrid resin preparation, coating
First the sodium carboxymethylcellulose powder of 20g is dissolved in 120g water, after fully dissolving and 100g water dispersant type polyaminoester resin carry out abundant mix and blend, add 0.5g bridging agent and 0.5g defoamer simultaneously, after fully stirring, form coating mixed resin liquid, surface at nylon base cloth is evenly coated with above-mentioned mixed resin liquid by coating machine, then passes through continuous drying case (70 ℃-90 ℃-130 ℃-150 ℃) drying and forming-film;
2. washing
The washing condition of setting cylinder rinsing machine is 70 ℃ × 40 minutes, and above-mentioned one-tenth film fabric is dropped into wherein, fully washed, by the sodium carboxymethylcellulose stripping in film;
3. dry, sizing
Finally one-tenth film fabric is dried to (120 ℃ × 2 minutes), sizing (170 ℃ × 1 minute) processing, obtains product of the present invention, its performance is in table 1.
Embodiment 6
1. hybrid resin preparation, coating
With embodiment 5;
2. washing
The washing condition of setting liquid-flow dyeing machine is 70 ℃ × 40 minutes, and the one-tenth film fabric that 1. step obtains drops into wherein, fully washing, by the sodium carboxymethylcellulose stripping in film;
3. dry, sizing
Finally one-tenth film fabric is dried to (120 ℃ × 2 minutes), sizing (170 ℃ × 1 minute) processing, obtains product of the present invention, its performance is in table 1.
Embodiment 7
1. hybrid resin preparation, coating
First the sodium carboxymethylcellulose powder of 30g is dissolved in 120g water, after fully dissolving and 100g water dispersant type polyaminoester resin carry out abundant mix and blend, add 0.5g bridging agent and 0.5g defoamer simultaneously, after fully stirring, form coating mixed resin liquid, surface at nylon base cloth is evenly coated with above-mentioned mixed resin liquid by coating machine, then passes through continuous drying case (70 ℃-90 ℃-130 ℃-150 ℃) drying and forming-film;
2. washing
The washing condition of setting liquid-flow dyeing machine is 70 ℃ × 40 minutes, and above-mentioned one-tenth film fabric is dropped into wherein, fully washed, by the sodium carboxymethylcellulose stripping in film;
3. dry, sizing
Finally one-tenth film fabric is dried to (120 ℃ × 2 minutes), sizing (170 ℃ × 1 minute) processing, obtains product of the present invention, its performance is in table 1.
Embodiment 8
1. hybrid resin preparation, coating
First the hydroxyethylcellulose powder of 10g is dissolved in 120g water, after fully dissolving and 100g water dispersant type polyaminoester resin carry out abundant mix and blend, add 0.5g bridging agent and 0.5g defoamer simultaneously, after fully stirring, form coating mixed resin liquid, surface at nylon base cloth is evenly coated with above-mentioned mixed resin liquid by coating machine, then passes through continuous drying case (70 ℃-90 ℃-130 ℃-150 ℃) drying and forming-film;
2. washing
The washing condition of setting liquid-flow dyeing machine is 70 ℃ × 40 minutes, and above-mentioned one-tenth film fabric is dropped into wherein, fully washed, by the hydroxyethylcellulose stripping in film;
3. dry, sizing
Finally one-tenth film fabric is dried to (120 ℃ × 2 minutes), sizing (170 ℃ × 1 minute) processing, obtains product of the present invention, its performance is in table 1.
Embodiment 9
1. hybrid resin preparation, coating
First the hydroxyethylcellulose powder of 20g is dissolved in 120g water, after fully dissolving and 100g water dispersant type polyaminoester resin carry out abundant mix and blend, add 0.5g bridging agent and 0.5g defoamer simultaneously, after fully stirring, form coating mixed resin liquid, surface at nylon base cloth is evenly coated with above-mentioned mixed resin liquid by coating machine, then passes through continuous drying case (70 ℃-90 ℃-130 ℃-150 ℃) drying and forming-film;
2. washing
The washing condition of setting liquid-flow dyeing machine is 70 ℃ × 40 minutes, and above-mentioned one-tenth film fabric is dropped into wherein, fully washed, by the hydroxyethylcellulose stripping in film;
3. dry, sizing
Finally one-tenth film fabric is dried to (120 ℃ × 2 minutes), sizing (170 ℃ × 1 minute) processing, obtains product of the present invention, its performance is in table 1.
Embodiment 10
1. hybrid resin preparation, coating
First the polyethylene glycol powder of 10g is dissolved in 120g water, after fully dissolving and 100g water dispersant type polyaminoester resin carry out abundant mix and blend, add 0.5g bridging agent and 0.5g defoamer simultaneously, after fully stirring, form coating mixed resin liquid, surface at nylon base cloth is evenly coated with above-mentioned mixed resin liquid by coating machine, then passes through continuous drying case (70 ℃-90 ℃-130 ℃-150 ℃) drying and forming-film;
2. washing
The washing condition of setting liquid-flow dyeing machine is 70 ℃ × 40 minutes, and above-mentioned one-tenth film fabric is dropped into wherein, fully washed, by the polyethylene glycol stripping in film;
3. dry, sizing
Finally one-tenth film fabric is dried to (120 ℃ × 2 minutes), sizing (170 ℃ × 1 minute) processing, obtains product of the present invention.Its performance is in table 1.
Embodiment 11
1. hybrid resin preparation, coating
First the polyvinylpyrrolidonepowder powder of 10g is dissolved in 120g water, after fully dissolving and 100g water dispersant type polyaminoester resin carry out abundant mix and blend, add 0.5g bridging agent and 0.5g defoamer simultaneously, after fully stirring, form coating mixed resin liquid, surface at nylon base cloth is evenly coated with above-mentioned mixed resin liquid by coating machine, then passes through continuous drying case (70 ℃-90 ℃-130 ℃-150 ℃) drying and forming-film;
2. washing
The washing condition of setting liquid-flow dyeing machine is 70 ℃ × 40 minutes, and above-mentioned one-tenth film fabric is dropped into wherein, fully washed, by the polyvinylpyrrolidone stripping in film;
3. dry, sizing
Finally one-tenth film fabric is dried to (120 ℃ × 2 minutes), sizing (170 ℃ × 1 minute) processing, obtains product of the present invention, its performance is in table 1.
Embodiment 12
1. hybrid resin preparation, coating
First the polyvinyl alcohol powder of 10g is dissolved in 120g water, after fully dissolving and 100g water dispersant type polyaminoester resin carry out abundant mix and blend, add 0.5g bridging agent and 0.5g defoamer simultaneously, after fully stirring, form coating mixed resin liquid, surface at nylon base cloth is evenly coated with above-mentioned mixed resin liquid by coating machine, then passes through continuous drying case (70 ℃-90 ℃-130 ℃-150 ℃) drying and forming-film;
2. washing
The washing condition of setting liquid-flow dyeing machine is 70 ℃ × 40 minutes, and above-mentioned one-tenth film fabric is dropped into wherein, fully washed, by the polyvinyl alcohol stripping in film;
3. dry, sizing
Finally one-tenth film fabric is dried to (120 ℃ × 2 minutes), sizing (170 ℃ × 1 minute) processing, obtains product of the present invention, its performance is in table 1.
Embodiment 13
1. hybrid resin preparation, coating
First the modified starch powder of 10g is dissolved in 120g water, after fully dissolving and 100g water dispersant type polyaminoester resin carry out abundant mix and blend, add 0.5g bridging agent and 0.5g defoamer simultaneously, after fully stirring, form coating mixed resin liquid, surface at nylon base cloth is evenly coated with above-mentioned mixed resin liquid by coating machine, then passes through continuous drying case (70 ℃-90 ℃-130 ℃-150 ℃) drying and forming-film;
2. washing
The washing condition of setting liquid-flow dyeing machine is 70 ℃ × 40 minutes, and above-mentioned one-tenth film fabric is dropped into wherein, fully washed, by the modified starch stripping in film;
3. dry, sizing
Finally one-tenth film fabric is dried to (120 ℃ × 2 minutes), sizing (170 ℃ × 1 minute) processing, obtains product of the present invention, its performance is in table 1.
Embodiment 14
1. hybrid resin preparation, coating
First the shitosan powder of 10g is dissolved in 120g water, after fully dissolving and 100g water dispersant type polyaminoester resin carry out abundant mix and blend, add 0.5g bridging agent and 0.5g defoamer simultaneously, after fully stirring, form coating mixed resin liquid, surface at nylon base cloth is evenly coated with above-mentioned mixed resin liquid by coating machine, then passes through continuous drying case (70 ℃-90 ℃-130 ℃-150 ℃) drying and forming-film;
2. washing
The washing condition of setting liquid-flow dyeing machine is 70 ℃ × 40 minutes, and coated fabric obtained above is dropped into wherein, fully washed, by the shitosan stripping in film;
3. dry, sizing
Finally one-tenth film fabric is dried to (120 ℃ × 2 minutes), sizing (170 ℃ × 1 minute) processing, obtains product of the present invention, its performance is in table 1.
Embodiment 15
1. hybrid resin preparation, coating
First the sodium carboxymethylcellulose powder of 20g is dissolved in 120g water, after fully dissolving and 100g water dispersant type polyaminoester resin carry out abundant mix and blend, add 0.5g bridging agent and 0.5g defoamer simultaneously, after fully stirring, form coating mixed resin liquid, surface at terylene base cloth is evenly coated with above-mentioned mixed resin liquid by coating machine, then passes through continuous drying case (70 ℃-90 ℃-130 ℃-150 ℃) drying and forming-film;
2. washing
The washing condition of setting liquid-flow dyeing machine is 70 ℃ × 40 minutes, and above-mentioned one-tenth film fabric is dropped into wherein, fully washed, by the sodium carboxymethylcellulose stripping in film;
3. dry, sizing
Finally one-tenth film fabric is dried to (120 ℃ × 2 minutes), sizing (170 ℃ × 1 minute) processing, obtains product of the present invention, its performance is in table 1.
Embodiment 16
1. hybrid resin preparation, coating
First the sodium carboxymethylcellulose powder of 20g is dissolved in 120g water, after fully dissolving and 100g water dispersant type polyaminoester resin carry out abundant mix and blend, add 0.5g bridging agent and 0.5g defoamer simultaneously, after fully stirring, form coating mixed resin liquid, surface at cotton base cloth is evenly coated with above-mentioned mixed resin liquid by coating machine, then passes through continuous drying case (70 ℃-90 ℃-130 ℃-150 ℃) drying and forming-film;
2. washing
The washing condition of setting liquid-flow dyeing machine is 70 ℃ × 40 minutes, and above-mentioned one-tenth film fabric is dropped into wherein, fully washed, by the sodium carboxymethylcellulose stripping in film;
3. dry, sizing
Finally one-tenth film fabric is dried to (120 ℃ × 2 minutes), sizing (170 ℃ × 1 minute) processing, obtains product of the present invention, its performance is in table 1.
Embodiment 17
1. hybrid resin preparation, coating
First the sodium carboxymethylcellulose powder of 20g is dissolved in 120g water, after fully dissolving and 100g water dispersant type polyaminoester resin carry out abundant mix and blend, add 0.5g bridging agent and 0.5g defoamer simultaneously, after fully stirring, form coating mixed resin liquid, surface at polyester-cotton blend base cloth is evenly coated with above-mentioned mixed resin liquid by coating machine, then passes through continuous drying case (70 ℃-90 ℃-130 ℃-150 ℃) drying and forming-film;
2. washing
The washing condition of setting liquid-flow dyeing machine is 70 ℃ × 40 minutes, and above-mentioned one-tenth film fabric is dropped into wherein, fully washed, by the sodium carboxymethylcellulose stripping in film;
3. dry, sizing
Finally one-tenth film fabric is dried to (120 ℃ × 2 minutes), sizing (170 ℃ × 1 minute) processing, obtains product of the present invention, its performance is in table 1.
Comparative example 1
1. resin preparation, coating
In 100g water dispersant type polyaminoester resin, add 0.5g bridging agent and 0.5g defoamer, after fully stirring, form coating resin liquid, surface at nylon base cloth is evenly coated with above-mentioned mixed resin liquid by coating machine, then passes through continuous drying case (70 ℃-90 ℃-130 ℃-150 ℃) drying and forming-film;
2. washing
The washing condition of setting liquid-flow dyeing machine is 90 ℃ × 60 minutes, and above-mentioned one-tenth film fabric is dropped into wherein, fully washed;
3. dry, sizing
Finally one-tenth film fabric is dried to (120 ℃ × 2 minutes), sizing (170 ℃ × 1 minute) processing, obtains product, its performance is in table 1.
Comparative example 2
1. resin preparation, coating
High triacontanol and 0.2 part of polyurethanes thickener of the soft soluble polyurethane that is 30% by 50 parts of solid contents by mass fraction, 0.1 part of neopelex, 0.2 part of lauryl sodium sulfate, 0.15 part of potassium laurate, 0.3 part of gelatin hydrolysate, 3 parts of 8~31 carbon atoms are mixed to get aqueous polyurethane mixed slurry, utilize inflation and the mechanical agitation of mechanical foaming machine to carry out physical blowing to aqueous polyurethane mixed slurry, obtain waterborne polyurethane foaming slurry; Surface at nylon base cloth is evenly coated with above-mentioned waterborne polyurethane foaming slurry by coating machine, then passes through drying box (170 ℃) drying and forming-film;
2. washing
Adopt water to rub the coating product washing 5 minutes that 1. machine obtain step at the hot water of 95 ℃, wash away the higher alcohols in polyurethane coating;
3. dry, sizing
Finally one-tenth film fabric is dried to (120 ℃ × 2 minutes), sizing (170 ℃ × 1 minute) processing, obtains product, its performance is in table 1.
Claims (6)
1. a production method for micro-porous film fabric, is characterized in that: comprise the steps:
1. the hybrid resin that at least contains water dispersant type polyaminoester and high molecular weight water soluble polymer is evenly coated to the surface of base cloth by the mode of coating, then drying and forming-film;
2. by washing, the high molecular weight water soluble polymer stripping in film is formed to microporous barrier again;
3. final drying sizing, obtains product.
2. the production method of micro-porous film fabric according to claim 1, is characterized in that: described high molecular weight water soluble polymer is sodium carboxymethylcellulose, polyethylene glycol, polyvinylpyrrolidone, polyvinyl alcohol, hydroxyethylcellulose, modified starch or shitosan.
3. according to the production method of the micro-porous film fabric described in claim 1, it is characterized in that: the content of described high molecular weight water soluble polymer is 5%~30%.
4. the production method of micro-porous film fabric according to claim 1, is characterized in that: the mode of described washing is cylinder washing or liquid-flow dyeing machine circulating water wash.
5. the production method of micro-porous film fabric according to claim 1, is characterized in that: the condition of described washing is 50~90 ℃ of temperature, 20~60 minutes time.
6. the production method of micro-porous film fabric according to claim 1, is characterized in that: described base cloth can be dacron, nylon fabrics, COTTON FABRIC or polyester-cotton fabric.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201210423405.7A CN103790021A (en) | 2012-10-30 | 2012-10-30 | Production method for micro porous membrane fabric |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201210423405.7A CN103790021A (en) | 2012-10-30 | 2012-10-30 | Production method for micro porous membrane fabric |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN103790021A true CN103790021A (en) | 2014-05-14 |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN106867017A (en) * | 2015-12-11 | 2017-06-20 | 东丽纤维研究所(中国)有限公司 | Controllable micro-porous film in a kind of aperture and preparation method thereof |
| CN107118607A (en) * | 2017-07-06 | 2017-09-01 | 四川粒界科技有限公司 | A kind of preparation method of high transmittance antireflective organic coating |
| CN108842469A (en) * | 2018-08-22 | 2018-11-20 | 晋江佰晟新材料科技有限公司 | A kind of preparation method of the anti-drilling pile fabric of waterproof and breathable |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN106867017A (en) * | 2015-12-11 | 2017-06-20 | 东丽纤维研究所(中国)有限公司 | Controllable micro-porous film in a kind of aperture and preparation method thereof |
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| CN107118607A (en) * | 2017-07-06 | 2017-09-01 | 四川粒界科技有限公司 | A kind of preparation method of high transmittance antireflective organic coating |
| CN108842469A (en) * | 2018-08-22 | 2018-11-20 | 晋江佰晟新材料科技有限公司 | A kind of preparation method of the anti-drilling pile fabric of waterproof and breathable |
| CN108842469B (en) * | 2018-08-22 | 2020-09-04 | 晋江佰晟新材料科技有限公司 | Preparation method of waterproof breathable down-proof fabric |
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