CN100404576C - Prepn process of nanometer starch crystal modified water-base polyurethane - Google Patents
Prepn process of nanometer starch crystal modified water-base polyurethane Download PDFInfo
- Publication number
- CN100404576C CN100404576C CNB2007100516566A CN200710051656A CN100404576C CN 100404576 C CN100404576 C CN 100404576C CN B2007100516566 A CNB2007100516566 A CN B2007100516566A CN 200710051656 A CN200710051656 A CN 200710051656A CN 100404576 C CN100404576 C CN 100404576C
- Authority
- CN
- China
- Prior art keywords
- polyether glycol
- add
- polyisocyanates
- polyester polyol
- starch crystal
- 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.)
- Expired - Fee Related
Links
Landscapes
- Polyurethanes Or Polyureas (AREA)
Abstract
The present invention is preparation process of nanometer starch crystal modified water-base polyurethane, and features that during synthesizing water-base polyurethane emulsion, nanometer starch crystal in the amount of 0.1-30 % total weight of polyisocyanate, polyester polyol and/or polyether polyol, and small molecular weight chain expander is added through one of three modes, including adding while adding small molecular weight chain expander, adding while adding icy water and adding directly into emulsified water-base polyurethane. The nanometer starch crystal modified water-base polyurethane has raised stretching strength and increased elongation at break.
Description
Technical field
The present invention relates to a kind of preparation method of modified aqueous polyurethane, belong to the biological nano field of compound material, also belong to the environment-friendly material field.
Background technology
Starch (starch) is a kind of natural macromolecule carbohydrate that is polymerized via the glucose molecule dehydration in photosynthesis by the many green plantss of nature, and its source is very extensive.The unit that forms have carbon 44.4%, hydrogen 6.2% and oxygen 49.4%, and its molecular formula is (C
6H
10O
5) n, wherein n is not for fixing a number, generally between 100-3000000.Starch can be divided into amylose starch and amylopectin.The n value of amylose starch is between the 100-6000, is generally 300-800; Amylopectin is the huge molecule of approximate pearl shape, and its n value is between 1000-3000000, generally more than 6000.Advantages such as that starch has is cheap, wide material sources, environmental protection now are widely used in food, medicine, weaving, papermaking and chemistry and other industry.
Nanoparticle also is ultrafine particle, generally is meant the particle of size between 1~1000nm, is the transitional region that is in cluster and macro object boundary.Nanoparticle has: effects such as surface effects, small-size effect and macroscopic quantum tunneling promptly have the character of special light, electromagnetism, mechanics and chemical aspect.Nanometer starch crystal (starch nanocrystal) be with the source abundant starch be that raw material obtains, with respect to inorganic nano-particle, nanometer starch crystal has following characteristics: at first, active hydroxyl is contained on its surface, can carry out chemical reaction or form strong intermolecular interaction; Secondly, it has biodegradable, physiologically acceptable and advantages of environment protection, helps protecting people's health and environment.At present, the research that nanometer starch crystal is used for filled polymer developing material new bio nano composite material receives much concern.Utilize nanometer starch crystal successfully modification rubber, starch plastic etc., improved intensity, hardness and the wear resistance of product.
Urethane is meant the multifunctional macromolecule synthetic materials that contains the carbamate base class in the molecular chain.It is divided into solvent borne polyurethane and aqueous polyurethane again, and wherein aqueous polyurethane more and more is subject to people's attention owing to have premium propertiess such as nontoxic, pollution-free.The aqueous polyurethane that contains single polyurethane structural, the performance of its film forming matter needs further to improve mechanical property for satisfying practical application more widely, and for this reason, it is necessary that aqueous polyurethane is carried out modification.But the resulting modified aqueous polyurethane of the method for existing modified aqueous polyurethane causes the decline of elongation at break usually when improving tensile strength.
Summary of the invention
The object of the present invention is to provide the preparation method of a kind of tensile strength height, nanometer starch crystal modified water-base polyurethane that elongation at break is high.
To achieve these goals, the technical solution adopted in the present invention following (3 kinds of schemes):
1. the preparation method of nanometer starch crystal modified water-base polyurethane is characterized in that it comprises the steps:
1). by polyisocyanates with following: one of a polyester polyol, b polyether glycol, three kinds of raw materials of the pure and mild polyether glycol of c polyester polyols mixed under 50-90 ℃ stirring reaction 2-5 hour, obtained polyurethane prepolymer; Wherein, polyisocyanates and polyester polyol or/and the mass percent of polyether glycol be respectively: polyisocyanates 65-90, polyester polyol is or/and polyether glycol 10-35; During the pure and mild polyether glycol of polyester polyols, the quality of polyester polyol and polyether glycol is any proportioning;
2). under 50-90 ℃, in the polyurethane prepolymer that step 1) obtains, add nanometer starch crystal and small molecule chain extender stirring reaction 1-3 hour, and use the butanone viscosity reduction, get substance A; Wherein, the add-on of small molecule chain extender is the 10-50% of polyisocyanates quality; The add-on of nanometer starch crystal is: a polyisocyanates, b polyester polyol are or/and the 0.1-30% of polyether glycol, three kinds of raw materials quality sums of c small molecule chain extender; The add-on of butanone is: a polyisocyanates, b polyester polyol are or/and the 10-30% of polyether glycol, three kinds of raw materials quality sums of c small molecule chain extender;
3). with step 2) substance A that obtains is cooled to below 40 ℃, adds neutralization reagent then, the adjusting pH value is 6-8, in and water-dispersion on the rocks again after 5-10 minute, vacuumize then and remove butanone, the mass percent of control solid content is 5-40%, product.
2. the preparation method of nanometer starch crystal modified water-base polyurethane is characterized in that it comprises the steps:
1). by polyisocyanates with following: one of a polyester polyol, b polyether glycol, three kinds of raw materials of the pure and mild polyether glycol of c polyester polyols mixed under 50-90 ℃ stirring reaction 2-5 hour, obtained polyurethane prepolymer; Wherein, polyisocyanates and polyester polyol or/and the mass percent of polyether glycol be respectively: polyisocyanates 65-90, polyester polyol is or/and polyether glycol 10-35; During the pure and mild polyether glycol of polyester polyols, the quality of polyester polyol and polyether glycol is any proportioning;
2). under 50-90 ℃, in the polyurethane prepolymer that step 1) obtains, add the small molecule chain extender stirring reaction 1-3 hour, and use the butanone viscosity reduction, get substance A; Wherein, the add-on of small molecule chain extender is the 10-50% of polyisocyanates quality; The add-on of butanone is: a polyisocyanates, b polyester polyol are or/and the 10-30% of polyether glycol, three kinds of raw materials quality sums of c small molecule chain extender;
3). with step 2) substance A that obtains is cooled to below 40 ℃, add neutralization reagent then, the adjusting pH value is 6-8, in and add nanometer starch crystal and frozen water after 5-10 minute again and disperse, the add-on of nanometer starch crystal is: a polyisocyanates, b polyester polyol are or/and the 0.1-30% of polyether glycol, three kinds of raw materials quality sums of c small molecule chain extender; Vacuumize then and remove butanone, the mass percent of control solid content is 5-40%, gets product.
3. the preparation method of nanometer starch crystal modified water-base polyurethane is characterized in that it comprises the steps:
1). by polyisocyanates with following: one of a polyester polyol, b polyether glycol, three kinds of raw materials of the pure and mild polyether glycol of c polyester polyols mixed under 50-90 ℃ stirring reaction 2-5 hour, obtained polyurethane prepolymer; Wherein, polyisocyanates and polyester polyol or/and the mass percent of polyether glycol be respectively: polyisocyanates 65-90, polyester polyol is or/and polyether glycol 10-35; During the pure and mild polyether glycol of polyester polyols, the quality of polyester polyol and polyether glycol is any proportioning;
2). under 50-90 ℃, in the polyurethane prepolymer that step 1) obtains, add the small molecule chain extender stirring reaction 1-3 hour, and use the butanone viscosity reduction, get substance A; Wherein, the add-on of small molecule chain extender is the 10-50% of polyisocyanates quality; The add-on of butanone is: a polyisocyanates, b polyester polyol are or/and the 10-30% of polyether glycol, three kinds of raw materials quality sums of c small molecule chain extender;
3). with step 2) substance A that obtains is cooled to below 40 ℃, adds neutralization reagent then, the adjusting pH value is 6-8, in and water-dispersion on the rocks again after 5-10 minute, aqueous polyurethane emulsion; Add the nanometer starch crystal blend in the aqueous polyurethane emulsion, the add-on of nanometer starch crystal is: a polyisocyanates, b polyester polyol are or/and the 0.1-30% of polyether glycol, three kinds of raw materials quality sums of c small molecule chain extender; Vacuumize then and remove butanone, the mass percent of control solid content is 5-40%, gets product.
Described small molecule chain extender is any one or any one the above mixing in dibasic alcohol, diamine, trivalent alcohol, the tertiary amine, is any proportioning during any one above mixing.
Described nanometer starch crystal is for being got the described sulphuric acid hydrolysis that is hydrolyzed to by the starch hydrolysis.
The preparation of described nanometer starch crystal: starch is scattered in 316mol L
-1H
2SO
4In, the quality of starch is H
2SO
4The content of liquor capacity is 15% (w/v), stirs five days down at 40 ℃ then, and stirring velocity is 100rpm; Water removes the upper strata stillness of night after surpassing centrifugation then, and repeated multiple times is about 7 until pH; The super centrifugal sediment that obtains is a nanometer starch crystal, and lyophilize gets the nanometer starch crystal powder.
Described neutralization reagent is triethylamine or hydrochloric acid.
Described starch is W-Gum, wheat starch, potato starch (comprising yam starch, tapioca (flour) or sweet potato starch etc.) or legume starch various natural plant starch such as (comprising pea starch, green starch etc.).
The present invention be by in the building-up process of aqueous polyurethane emulsion, add nanometer starch crystal (nanometer starch crystal is introduced by three kinds of modes: the one, when adding the small molecules chain extension, add simultaneously; The 2nd, the frozen water during with emulsification adds simultaneously; The 3rd, directly add in the aqueous polyurethane emulsion that emulsification finishes), the mechanical property that its emulsion is solidified the mould material that the back forms significantly improves (tensile strength height, elongation at break height).Nanometer starch crystal among the present invention is to be got by starch (as yam starch or W-Gum) hydrolysis, yam starch and W-Gum all are reproducible natural polymers, with low cost, the source is abundant, and preparation, extract nanometer starch crystal the processing condition process simple.Aqueous polyurethane is a kind of ep-type material, that the present invention will originate will be abundant, the simple nanometer starch crystal of technology combines the material that has not only obtained improved performance with environment-friendly water-based polyurethane, also improved the using value of starch, expanded its use range, its low production cost and have environmental protection, biodegradable characteristics simultaneously, and technology of the present invention is simple, therefore has higher scientific and technological content.All be significantly improved before the relative modification of the tensile strength of the resulting nanometer starch crystal modified water-base polyurethane of this method, can be used as materials such as film, coating, tackiness agent with elongation at break.
Embodiment
In order to understand the present invention better, further illustrate content of the present invention below in conjunction with embodiment, but content of the present invention not only is confined to the following examples.
Embodiment 1:
A kind of preparation method of nanometer starch crystal modified water-base polyurethane, it comprises the steps:
1). with polyester diol (the poly-hexanodioic acid-1 of calculated amount, the 4-butanediol ester, molecular weight 2000, Yantai China is big) and tolylene diisocyanate (TDI, Shanghai chemical reagents corporation of Chinese Medicine group) is blended in 70 ℃ of following stirring reactions 2 hours, gets polyurethane prepolymer; The mass percent of polyester diol and tolylene diisocyanate is: polyester diol 20, tolylene diisocyanate 80;
2). under 85 ℃, in polyurethane prepolymer, add small molecule chain extender: 2,2 '-dimethylol propionic acid (DMPA, Huzhou is long contains), the add-on of small molecule chain extender DMPA is 20% of a tolylene diisocyanate quality, stirring reaction 1 hour, and use butanone viscosity reduction, the add-on of butanone be polyester diol, tolylene diisocyanate and 2,2 '-the dimethylol propionic acid total mass 10%;
3). after reaction was finished, temperature dropped to (as 0-39 ℃) below 40 ℃, and addings waits in the triethylamine (TEA, Chengdu section dragon) of DMPA molar weight and salify 5 minutes again, the add-on of triethylamine (TEA) identical with the amount of DMPA (the adjusting pH value is within the 6-8 scope); Under high-speed stirring (2000-4000 rev/min), the adding of nanometer starch crystal frozen water solution is disperseed; The nanometer starch crystal add-on be polyester diol, tolylene diisocyanate and 2,2 '-the dimethylol propionic acid total mass 6%; Vacuumize then and remove butanone and obtain nanometer starch crystal modified water-base polyurethane (or claim nanometer starch crystal composite aqueous polyurethane emulsion); The solid content of nanometer starch crystal composite aqueous polyurethane emulsion is in 15% (by the water yield control that adds);
4). under 60 ℃, with nanometer starch crystal composite aqueous polyurethane emulsion casting film-forming on polyfluortetraethylene plate.
After the mould material cut-parts, be 35% at constant humidity, place after 7 days under the room temperature and carry out performance test.The mechanical property of the sheet material of preparation sees Table 1.Mechanical property thinks carefully newly in Shenzhen with reference to State Standard of the People's Republic of China GB4456-84 on the CMT6503 instrument of testing tool company and records that rate of extension is 300mm/min.
Embodiment 2:
Substantially the same manner as Example 1, difference is: the nanometer starch crystal of interpolation is polyester diol, tolylene diisocyanate and 2,2 '-the dimethylol propionic acid total mass 10%, obtain nanometer starch crystal modified water-base polyurethane (or claim nanometer starch crystal composite aqueous polyurethane emulsion).The mechanical property of the sheet material of preparation sees Table 1.Mechanics Performance Testing is with embodiment 1.
Embodiment 3:
A kind of preparation method of nanometer starch crystal modified water-base polyurethane, it comprises the steps:
1). the polyester diol (molecular weight 2000) and the tolylene diisocyanate (TDI) of calculated amount are blended in 70 ℃ of following stirring reactions 2 hours, get polyurethane prepolymer; The mass percent of polyester diol and tolylene diisocyanate is: polyester diol 35, tolylene diisocyanate 65;
2). in the polyurethane prepolymer that step 1) obtains, adding small molecule chain extender under 85 ℃: 2,2 '-dimethylol propionic acid (DMPA, Huzhou is long contains), the add-on of small molecule chain extender DMPA is 50% of a tolylene diisocyanate quality, stirring reaction 1 hour, use the butanone viscosity reduction during this time, the add-on of butanone be polyester diol, tolylene diisocyanate and 2,2 '-the dimethylol propionic acid total mass 20%;
3). after reaction is finished, reduce the temperature to below 40 ℃, adding waits in the triethylamine (TEA) of DMPA molar weight and salify 5 minutes again, the add-on of triethylamine (TEA) identical with the amount of DMPA (regulating pH value within the 6-8 scope), add frozen water down in high-speed stirring (2000-4000 rev/min) and disperse, get aqueous polyurethane emulsion; With the nanometer starch crystal aqueous solution and the aqueous polyurethane emulsion blend that obtains, the nanometer starch crystal add-on be polyester diol, tolylene diisocyanate and 2,2 '-the dimethylol propionic acid total mass 6%; Vacuumize then and remove butanone and obtain nanometer starch crystal modified water-base polyurethane (or claim nanometer starch crystal composite aqueous polyurethane emulsion); The solid content of control nanometer starch crystal composite aqueous polyurethane emulsion is in 30% (by the water yield control that adds);
4). under 60 ℃, with emulsion casting film-forming on polyfluortetraethylene plate.
After the mould material cut-parts, be 35% at constant humidity, place after 7 days under the room temperature and carry out performance test.The mechanical property of the sheet material of preparation sees Table 1.Mechanics Performance Testing is with embodiment 1.
Embodiment 4:
Substantially the same manner as Example 3, difference is: the content of the nanometer starch crystal of interpolation is polyester diol, tolylene diisocyanate and 2,2 '-the dimethylol propionic acid total mass 10%, obtain nanometer starch crystal modified water-base polyurethane, the mechanical property of the sheet material of preparation sees Table 1.Mechanics Performance Testing is with embodiment 1.
Embodiment 5:
A kind of preparation method of nanometer starch crystal modified water-base polyurethane, it comprises the steps:
1). the polyester diol (molecular weight 2000) and the tolylene diisocyanate (TDI) of calculated amount are blended in 70 ℃ of stirring reactions 2 hours, get polyurethane prepolymer; The mass percent of polyester diol and tolylene diisocyanate is: polyester diol 25, tolylene diisocyanate 75;
2). in the polyurethane prepolymer that step 1) obtains, adding small molecule chain extender under 85 ℃: 2,2 '-dimethylol propionic acid (DMPA, Huzhou is long contains), the add-on of small molecule chain extender DMPA is 30% of a tolylene diisocyanate quality, stirring reaction 1 hour, use the butanone viscosity reduction during this time, the add-on of butanone is the quality polyester diol, tolylene diisocyanate and 2,2 '-the dimethylol propionic acid total mass 25%, in this stage nanometer starch crystal is dissolved in the butanone through ultra-sonic dispersion and adds in the reaction unit, the add-on of nanometer starch crystal is a polyester diol, tolylene diisocyanate and 2,2 '-the dimethylol propionic acid total mass 6%.
3). after finishing, reaction reduces the temperature to below 40 ℃, adding waits in the triethylamine (TEA) of DMPA molar weight and salify 5 minutes again, the add-on of triethylamine (TEA) identical with the amount of DMPA (regulating pH value within the 6-8 scope) adds frozen water and disperses under high-speed stirring; Vacuumize then and remove butanone and obtain nanometer starch crystal modified water-base polyurethane (or claim nanometer starch crystal composite aqueous polyurethane emulsion); The solid content of control emulsion is in 20% (by the water yield control that adds);
4). under 60 ℃, with emulsion casting film-forming on polyfluortetraethylene plate.
After the mould material cut-parts, be 35% at constant humidity, place after 7 days under the room temperature and carry out performance test.The mechanical property of the sheet material of preparation sees Table 1.Mechanics Performance Testing is with embodiment 1.
Embodiment 6:
Substantially the same manner as Example 5, difference is: the content of the nanometer starch crystal of interpolation is polyester diol, tolylene diisocyanate and 2,2 '-the dimethylol propionic acid total mass 8%, obtain nanometer starch crystal modified water-base polyurethane (or claim nanometer starch crystal composite aqueous polyurethane emulsion).The mechanical property of the sheet material of preparation sees Table 1.Mechanics Performance Testing is with embodiment 1.
Embodiment 7:
Substantially the same manner as Example 5, difference is: the content of the nanometer starch crystal of interpolation be polyester diol, tolylene diisocyanate and 2,2 '-the dimethylol propionic acid total mass 10%, obtain nanometer starch crystal composite aqueous polyurethane emulsion.The mechanical property of the sheet material of preparation sees Table 1.Mechanics Performance Testing is with embodiment 1.
Embodiment 8:
A kind of preparation method of nanometer starch crystal modified water-base polyurethane, it comprises the steps:
1). the polyester diol (molecular weight 2000) and the tolylene diisocyanate (TDI) of calculated amount are blended in 70 ℃ of stirring reactions 2 hours, get polyurethane prepolymer; The mass percent of polyester diol and tolylene diisocyanate is: polyester diol 30, tolylene diisocyanate 70;
2). in the polyurethane prepolymer that step 1) obtains, adding small molecule chain extender DMPA under 70 ℃, the add-on of small molecule chain extender DMPA is 35% of a tolylene diisocyanate quality, stirring reaction 1 hour, use the butanone viscosity reduction during this time, the add-on of butanone is 30% of polyester diol, tolylene diisocyanate and a small molecule chain extender DMPA total mass;
3). reaction reduces the temperature to below 40 ℃ after finishing, and addings waits in the triethylamine (TEA) of DMPA molar weight and salify 5 minutes again, the add-on of triethylamine (TEA) identical with the amount of DMPA (the adjusting pH value is within the 6-8 scope); Adding nanometer starch crystal frozen water solution under high-speed stirring disperses; The add-on of nanometer starch crystal is 3.0% of polyester diol, tolylene diisocyanate and a small molecule chain extender DMPA total mass; Vacuumize then and remove butanone and obtain nanometer starch crystal composite aqueous polyurethane emulsion; The solid content of control emulsion is in 30% (by the water yield control that adds);
4). under 60 ℃, with emulsion casting film-forming on polyfluortetraethylene plate.
After the mould material cut-parts, be 35% at constant humidity, place after 7 days under the room temperature and carry out performance test.The mechanical property of the sheet material of preparation sees Table 1.Mechanics Performance Testing is with embodiment 1.
Embodiment 9:
A kind of preparation method of nanometer starch crystal modified water-base polyurethane, it comprises the steps:
1). the polyester diol (molecular weight 2000) and the tolylene diisocyanate (TDI) of calculated amount are blended in 50 ℃ of stirring reactions 5 hours, get polyurethane prepolymer; The mass percent of polyester diol and tolylene diisocyanate is: polyester diol 15, tolylene diisocyanate 85;
2). in the polyurethane prepolymer that step 1) obtains, adding small molecule chain extender DMPA under 90 ℃, the add-on of small molecule chain extender DMPA is 40% of a tolylene diisocyanate quality, stirring reaction 3 hours, use the butanone viscosity reduction during this time, the add-on of butanone is 15% of polyester diol, tolylene diisocyanate and a small molecule chain extender DMPA total mass;
3). after finishing, reaction reduces the temperature to (as 0-30 ℃) below 40 ℃, adding waits in the triethylamine (TEA) of DMPA molar weight and salify 5 minutes then, the add-on of triethylamine (TEA) identical with the amount of DMPA (regulating pH value within the 6-8 scope), adding frozen water under high-speed stirring disperses, get aqueous polyurethane emulsion, at this moment the NCO/OH=1.75 of emulsion; Aqueous polyurethane emulsion blend nanometer starch crystal is soluble in water and obtain, the add-on of nanometer starch crystal is 3.0% of polyester diol, tolylene diisocyanate and a small molecule chain extender DMPA total mass; Vacuumize then and remove butanone and obtain nanometer starch crystal modified water-base polyurethane (or claim nanometer starch crystal composite aqueous polyurethane emulsion), the solid content of control mixed emulsion is in 40% (by the water yield control that adds);
4). under 60 ℃, with emulsion casting film-forming on polyfluortetraethylene plate.
After the mould material cut-parts, be 35% at constant humidity, place after 7 days under the room temperature and carry out performance test.The mechanical property of the sheet material of preparation sees Table 1.Mechanics Performance Testing is with embodiment 1.
Comparative example 1:
Substantially the same manner as Example 1, difference only is not add nanometer starch crystal.The mechanical property of the sheet material of preparation sees Table 1.Mechanics Performance Testing is with embodiment 1.
Embodiment 10:
Substantially the same manner as Example 1, difference is: the raw material of aqueous polyurethane is polyoxypropyleneglycol (PPG, molecular weight 2000, Nanjing Zhong Shan) and 4,4 '-diphenylmethanediisocyanate (MDI, Yantai China is big), the NCO/OH=3.0 of nanometer starch crystal composite aqueous polyurethane emulsion, chainextender is tetramethylolmethane (Pnta, suitableization of a Hubei company), and neutralization reagent is hydrochloric acid (a Shanghai chemical reagents corporation of Chinese Medicine group); The content of the nanometer starch crystal that adds be polyoxypropyleneglycol, 4,4 '-diphenylmethanediisocyanate and tetramethylolmethane total mass 30%, obtain nanometer starch crystal modified water-base polyurethane (or claiming nanometer starch crystal composite aqueous polyurethane emulsion).
Embodiment 11:
Substantially the same manner as Example 3, difference is: the raw material of aqueous polyurethane is polytetramethylene ether diol (PTMEG, molecular weight 2000) with hexamethylene diisocyanate (HDI) mixture, the NCO/OH=1.70 of nanometer starch crystal composite aqueous polyurethane emulsion, chainextender is a diethylenetriamine, and neutralization reagent is a hydrochloric acid; The content of the nanometer starch crystal that adds is 0.5% of polytetramethylene ether diol, hexamethylene diisocyanate and diethylenetriamine total mass, obtains nanometer starch crystal modified water-base polyurethane (or claiming nanometer starch crystal composite aqueous polyurethane emulsion).
Embodiment 12:
A kind of preparation method of nanometer starch crystal modified water-base polyurethane, it comprises the steps:
1). with the polyester polyol (molecular weight 3000 of calculated amount, Yantai China is big) and polyether glycol (molecular weight 1000, the big chemical industry in Shandong east) mixture and hexamethylene diisocyanate (HDI, German Bayer) be 70 ℃ of stirring reactions 2 hours, polyurethane prepolymer; The mass percent of polyester polyol and polyether glycol mixture and hexamethylene diisocyanate is: polyester polyol and polyether glycol mixture 25, hexamethylene diisocyanate 75; Wherein, the shared mass percent of polyester polyol is 10, and the shared mass percent of polyether glycol is 15;
2). in the polyurethane prepolymer that step 1) obtains, adding small molecule chain extender under 85 ℃: diethylenetriamine (occasion are praised in Shanghai), the add-on of diethylenetriamine is 30% of a hexamethylene diisocyanate quality, stirring reaction 1 hour, use the butanone viscosity reduction during this time, the add-on of butanone is a polyester polyol, polyether glycol, 25% of hexamethylene diisocyanate and diethylenetriamine total mass, in this stage nanometer starch crystal is dissolved in the butanone through ultra-sonic dispersion and adds in the reaction unit, the add-on of nanometer starch crystal is a polyester polyol, polyether glycol, 15% of hexamethylene diisocyanate and diethylenetriamine total mass.
3). after finishing, reaction reduces the temperature to below 40 ℃, again in the hydrochloric acid of diethylenetriamine molar weight such as adding and salify 5 minutes, the add-on of hydrochloric acid identical with the amount of diethylenetriamine (regulating pH value within the 6-8 scope) adds frozen water and disperses under high-speed stirring; Vacuumize then and remove butanone and obtain nanometer starch crystal modified water-base polyurethane (or claim nanometer starch crystal composite aqueous polyurethane emulsion); The solid content of control emulsion is in 20% (by the water yield control that adds).
Embodiment 13:
A kind of preparation method of nanometer starch crystal modified water-base polyurethane, it comprises the steps:
1). the polyether glycol (molecular weight 3000) and the isophorone diisocyanate (IPDI, German Bayer) of calculated amount are blended in 70 ℃ of following stirring reactions 2 hours, get polyurethane prepolymer; The mass percent of polyether glycol, isophorone diisocyanate is: polyether glycol 35, isophorone diisocyanate 65;
2). in the polyurethane prepolymer that step 1) obtains, adding small molecule chain extender under 85 ℃: 1,4-butyleneglycol (BDO, Dushanzi, Xinjiang petrochemical industry), 1, the add-on of 4-butyleneglycol is 50% of an isophorone diisocyanate quality, stirring reaction 1 hour, during use the butanone viscosity reduction, the add-on of butanone is polyether glycol, isophorone diisocyanate and 1,20% of 4-butyleneglycol total mass;
3). after reaction is finished, reduce the temperature to below 40 ℃, add again and wait 1, in the hydrochloric acid of 4-butyleneglycol molar weight and salify 5 minutes, the add-on of hydrochloric acid and 1, the amount of 4-butyleneglycol identical (regulating pH value within the 6-8 scope) adds frozen water down in high-speed stirring (2000-4000 rev/min) and disperses, and gets aqueous polyurethane emulsion; With the nanometer starch crystal aqueous solution and the aqueous polyurethane emulsion blend that obtains, the nanometer starch crystal add-on is polyether glycol, isophorone diisocyanate and 1,1% of 4-butyleneglycol total mass; Vacuumize then and remove butanone and obtain nanometer starch crystal modified water-base polyurethane (or claim nanometer starch crystal composite aqueous polyurethane emulsion); The solid content of control nanometer starch crystal composite aqueous polyurethane emulsion is in 30% (by the water yield control that adds).
Embodiment 14:
A kind of preparation method of nanometer starch crystal modified water-base polyurethane, it comprises the steps:
1). with the polyester polyol (molecular weight 2000) and the polyether glycol (molecular weight 1000 of calculated amount, the Zhong Mountain, Nanjing petrochemical industry) mixture and 4,4 '-diphenylmethanediisocyanate (MDI, Yantai China is big) with tolylene diisocyanate (TDI) mixture 70 ℃ of following stirring reactions 2 hours, polyurethane prepolymer; Polyester polyol, polyether glycol, 4,4 '-mass percent of diphenylmethanediisocyanate, tolylene diisocyanate is: polyether glycol 15, polyester polyol 20,4,4 '-diphenylmethanediisocyanate 40, tolylene diisocyanate 25;
2). in the polyurethane prepolymer that step 1) obtains, adding small molecule chain extender under 85 ℃: diethylenetriamine, the add-on of diethylenetriamine is 4,4 '-diphenylmethanediisocyanate and tolylene diisocyanate quality 50%, stirring reaction 1 hour, use the butanone viscosity reduction during this time, the add-on of butanone be polyester polyol, polyether glycol, 4,4 '-diphenylmethanediisocyanate, tolylene diisocyanate and diethylenetriamine total mass 20%;
3). after reaction is finished, reduce the temperature to below 40 ℃, again in the hydrochloric acid of diethylenetriamine molar weight such as adding and salify 5 minutes, the add-on of hydrochloric acid identical with the amount of diethylenetriamine (regulating pH value within the 6-8 scope), add frozen water down in high-speed stirring (2000-4000 rev/min) and disperse, get aqueous polyurethane emulsion; With the nanometer starch crystal aqueous solution and the aqueous polyurethane emulsion blend that obtains, the nanometer starch crystal add-on be polyester polyol, polyether glycol, 4,4 '-diphenylmethanediisocyanate, tolylene diisocyanate and diethylenetriamine total mass 25%; Vacuumize then and remove butanone and obtain nanometer starch crystal modified water-base polyurethane (or claim nanometer starch crystal composite aqueous polyurethane emulsion); The solid content of control nanometer starch crystal composite aqueous polyurethane emulsion is in 30% (by the water yield control that adds).
Embodiment 15:
A kind of preparation method of nanometer starch crystal modified water-base polyurethane, it comprises the steps:
1). with polyester diol (the poly-hexanodioic acid-1 of calculated amount, the 4-butanediol ester, molecular weight 2000, Yantai China is big) and tolylene diisocyanate (TDI, Shanghai chemical reagents corporation of Chinese Medicine group) is blended in 50 ℃ of following stirring reactions 5 hours, gets polyurethane prepolymer; The mass percent of polyester diol and tolylene diisocyanate is: polyester diol 10, tolylene diisocyanate 90; 2). under 50 ℃, in polyurethane prepolymer, add small molecule chain extender: 2,2 '-dimethylol propionic acid (DMPA, Huzhou is long contains), the add-on of small molecule chain extender DMPA is 20% of a tolylene diisocyanate quality, stirring reaction 3 hours, and use butanone viscosity reduction, the add-on of butanone be polyester diol, tolylene diisocyanate and 2,2 '-the dimethylol propionic acid total mass 50%;
3). after reaction was finished, temperature dropped to (as 0-39 ℃) below 40 ℃, and addings waits in the triethylamine (TEA, Chengdu section dragon) of DMPA molar weight and salify 5 minutes again, the add-on of triethylamine (TEA) identical with the amount of DMPA (the adjusting pH value is within the 6-8 scope); Under high-speed stirring (2000-4000 rev/min), the adding of nanometer starch crystal frozen water solution is disperseed; The nanometer starch crystal add-on be polyester diol, tolylene diisocyanate and 2,2 '-the dimethylol propionic acid total mass 0.1%; Vacuumize then and remove butanone and obtain nanometer starch crystal modified water-base polyurethane (or claim nanometer starch crystal composite aqueous polyurethane emulsion); The solid content of nanometer starch crystal composite aqueous polyurethane emulsion is in 15% (by the water yield control that adds).
Embodiment 16:
Substantially the same manner as Example 1, difference is: the nanometer starch crystal add-on be polyester diol, tolylene diisocyanate and 2,2 '-the dimethylol propionic acid total mass 30%.
Embodiment 17:
Substantially the same manner as Example 5, difference is: the add-on of nanometer starch crystal be polyester diol, tolylene diisocyanate and 2,2 '-the dimethylol propionic acid total mass 30%.
Embodiment 18:
Substantially the same manner as Example 8, difference is: the add-on of nanometer starch crystal is 30% of polyester diol, tolylene diisocyanate and a small molecule chain extender DMPA total mass.
The mechanical property of subordinate list 1. nanometer starch crystal composite aqueous polyurethanes
Conclusion:
1. compare with comparative example 1, the mechanical property of other examples of implementation (tensile strength, elongation at break) all is significantly improved;
2. relatively can find that along with the increase of nanometer starch crystal content, its tensile strength increases gradually by embodiment 9,3,4, elongation at break reduces;
3. can find relatively by embodiment 8,1,2 that along with the increase of nanometer starch crystal content, its tensile strength is by all reducing with elongation at break; Equally, can lead to the same conclusion by embodiment 5,6,7;
4. in the feed way of three kinds of nanometer starch crystal composite aqueous polyurethanes, preceding two kinds of feed way are more obvious to the raising of tensile strength performance than the third mode.
Claims (3)
1. the preparation method of nanometer starch crystal modified water-base polyurethane is characterized in that it comprises the steps:
1). by polyisocyanates with following: one of a polyester polyol, b polyether glycol, three kinds of raw materials of the pure and mild polyether glycol of c polyester polyols mixed under 50-90 ℃ stirring reaction 2-5 hour, obtained polyurethane prepolymer; Wherein, polyisocyanates and polyester polyol or/and the mass percent of polyether glycol be respectively: polyisocyanates 65-90, polyester polyol is or/and polyether glycol 10-35; During the pure and mild polyether glycol of polyester polyols, the quality of polyester polyol and polyether glycol is any proportioning;
2). under 50-90 ℃, in the polyurethane prepolymer that step 1) obtains, add nanometer starch crystal and small molecule chain extender stirring reaction 1-3 hour, and use the butanone viscosity reduction, get substance A; Wherein, the add-on of small molecule chain extender is the 10-50% of polyisocyanates quality; The add-on of nanometer starch crystal is: a polyisocyanates, b polyester polyol are or/and the 0.1-30% of polyether glycol, three kinds of raw materials quality sums of c small molecule chain extender; The add-on of butanone is: a polyisocyanates, b polyester polyol are or/and the 10-30% of polyether glycol, three kinds of raw materials quality sums of c small molecule chain extender;
3). with step 2) substance A that obtains is cooled to below 40 ℃, adds neutralization reagent then, the adjusting pH value is 6-8, in and water-dispersion on the rocks again after 5-10 minute, vacuumize then and remove butanone, the mass percent of control solid content is 5-40%, product.
2. the preparation method of nanometer starch crystal modified water-base polyurethane is characterized in that it comprises the steps:
1). by polyisocyanates with following: one of a polyester polyol, b polyether glycol, three kinds of raw materials of the pure and mild polyether glycol of c polyester polyols mixed under 50-90 ℃ stirring reaction 2-5 hour, obtained polyurethane prepolymer; Wherein, polyisocyanates and polyester polyol or/and the mass percent of polyether glycol be respectively: polyisocyanates 65-90, polyester polyol is or/and polyether glycol 10-35; During the pure and mild polyether glycol of polyester polyols, the quality of polyester polyol and polyether glycol is any proportioning;
2). under 50-90 ℃, in the polyurethane prepolymer that step 1) obtains, add the small molecule chain extender stirring reaction 1-3 hour, and use the butanone viscosity reduction, get substance A; Wherein, the add-on of small molecule chain extender is the 10-50% of polyisocyanates quality; The add-on of butanone is: a polyisocyanates, b polyester polyol are or/and the 10-30% of polyether glycol, three kinds of raw materials quality sums of c small molecule chain extender;
3). with step 2) substance A that obtains is cooled to below 40 ℃, add neutralization reagent then, the adjusting pH value is 6-8, in and add nanometer starch crystal and frozen water after 5-10 minute again and disperse, the add-on of nanometer starch crystal is: a polyisocyanates, b polyester polyol are or/and the 0.1-30% of polyether glycol, three kinds of raw materials quality sums of c small molecule chain extender; Vacuumize then and remove butanone, the mass percent of control solid content is 5-40%, gets product.
3. the preparation method of nanometer starch crystal modified water-base polyurethane is characterized in that it comprises the steps:
1). by polyisocyanates with following: one of a polyester polyol, b polyether glycol, three kinds of raw materials of the pure and mild polyether glycol of c polyester polyols mixed under 50-90 ℃ stirring reaction 2-5 hour, obtained polyurethane prepolymer; Wherein, polyisocyanates and polyester polyol or/and the mass percent of polyether glycol be respectively: polyisocyanates 65-90, polyester polyol is or/and polyether glycol 10-35; During the pure and mild polyether glycol of polyester polyols, the quality of polyester polyol and polyether glycol is any proportioning;
2). under 50-90 ℃, in the polyurethane prepolymer that step 1) obtains, add the small molecule chain extender stirring reaction 1-3 hour, and use the butanone viscosity reduction, get substance A; Wherein, the add-on of small molecule chain extender is the 10-50% of polyisocyanates quality; The add-on of butanone is: a polyisocyanates, b polyester polyol are or/and the 10-30% of polyether glycol, three kinds of raw materials quality sums of c small molecule chain extender;
3). with step 2) substance A that obtains is cooled to below 40 ℃, adds neutralization reagent then, the adjusting pH value is 6-8, in and water-dispersion on the rocks again after 5-10 minute, aqueous polyurethane emulsion; Add the nanometer starch crystal blend in the aqueous polyurethane emulsion, the add-on of nanometer starch crystal is: a polyisocyanates, b polyester polyol are or/and the 0.1-30% of polyether glycol, three kinds of raw materials quality sums of c small molecule chain extender; Vacuumize then and remove butanone, the mass percent of control solid content is 5-40%, gets product.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2007100516566A CN100404576C (en) | 2007-03-13 | 2007-03-13 | Prepn process of nanometer starch crystal modified water-base polyurethane |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2007100516566A CN100404576C (en) | 2007-03-13 | 2007-03-13 | Prepn process of nanometer starch crystal modified water-base polyurethane |
Publications (2)
Publication Number | Publication Date |
---|---|
CN101020739A CN101020739A (en) | 2007-08-22 |
CN100404576C true CN100404576C (en) | 2008-07-23 |
Family
ID=38708626
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB2007100516566A Expired - Fee Related CN100404576C (en) | 2007-03-13 | 2007-03-13 | Prepn process of nanometer starch crystal modified water-base polyurethane |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN100404576C (en) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101230189B (en) * | 2008-01-29 | 2010-06-02 | 武汉理工大学 | Method for preparing polysaccharide nano-crystalline grafted polyester modified polyurethane material |
CN102604363B (en) * | 2012-03-07 | 2013-06-12 | 武汉理工大学 | Preparation method of polyurethane nanometer composites |
FR2996848B1 (en) * | 2012-10-16 | 2014-10-31 | Agronomique Inst Nat Rech | COMPOSITION COMPRISING AN INTERNAL PHASE DISPERSE IN A HYDROPHILIC CONTINUOUS PHASE |
CN103709366A (en) * | 2013-12-20 | 2014-04-09 | 天津商业大学 | Preparation method of anti-yellowing compound surface sizing agent |
CN104263269B (en) * | 2014-09-10 | 2016-08-24 | 上海金大塑胶有限公司 | A kind of composite |
CN104263275B (en) * | 2014-09-10 | 2016-08-24 | 上海金大塑胶有限公司 | A kind of environment-friendly type adhesive label material |
CN104877540A (en) * | 2015-05-06 | 2015-09-02 | 广德加点化工有限公司 | Impact-resistant and tear-resistant water-based paint |
CN104877534A (en) * | 2015-05-06 | 2015-09-02 | 广德加点化工有限公司 | Waterproof and high-strength water-based paint |
CN112143210B (en) * | 2020-08-28 | 2022-05-27 | 东莞市吉鑫高分子科技有限公司 | Amphiphilic biodegradable thermoplastic polyurethane elastomer and preparation method thereof |
CN113652008A (en) * | 2021-09-18 | 2021-11-16 | 安徽乐朗环保新材料有限公司 | Degradable starch plastic composition and preparation method and application thereof |
CN115074013A (en) * | 2022-08-19 | 2022-09-20 | 南通宸康新材料科技有限公司 | Antibacterial flexibility-increasing surface treating agent and preparation method thereof |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1077725A (en) * | 1993-04-20 | 1993-10-27 | 王笃伦 | Rigid foam glucose polyurethane plastics and production method thereof |
JP2001247835A (en) * | 2000-03-03 | 2001-09-14 | Nippon Nsc Ltd | Aqueous adhesive |
US20020031669A1 (en) * | 1999-05-18 | 2002-03-14 | Gang-Fung Chen | Heat and radio frequency-curable two-pack soy protein-based polyurethane adhesive compositions |
CN1876746A (en) * | 2006-07-10 | 2006-12-13 | 武汉理工大学 | Natural macromolecular composite aqueous polyurethane bond and its preparation method |
-
2007
- 2007-03-13 CN CNB2007100516566A patent/CN100404576C/en not_active Expired - Fee Related
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1077725A (en) * | 1993-04-20 | 1993-10-27 | 王笃伦 | Rigid foam glucose polyurethane plastics and production method thereof |
US20020031669A1 (en) * | 1999-05-18 | 2002-03-14 | Gang-Fung Chen | Heat and radio frequency-curable two-pack soy protein-based polyurethane adhesive compositions |
JP2001247835A (en) * | 2000-03-03 | 2001-09-14 | Nippon Nsc Ltd | Aqueous adhesive |
CN1876746A (en) * | 2006-07-10 | 2006-12-13 | 武汉理工大学 | Natural macromolecular composite aqueous polyurethane bond and its preparation method |
Non-Patent Citations (2)
Title |
---|
聚氨酯/ 壳聚糖互穿聚合物网络涂层再生纤维素膜的生物降解性. 周金平.纤维素科学与技术,第8卷第3期. 2000 |
聚氨酯/ 壳聚糖互穿聚合物网络涂层再生纤维素膜的生物降解性. 周金平.纤维素科学与技术,第8卷第3期. 2000 * |
Also Published As
Publication number | Publication date |
---|---|
CN101020739A (en) | 2007-08-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN100404576C (en) | Prepn process of nanometer starch crystal modified water-base polyurethane | |
CN100478375C (en) | Production of lignin modified water polyurethane | |
CN103881049B (en) | The preparation method of eleostearic acid monoglyceride modified aqueous polyurethane emulsion | |
CN101942071B (en) | Polyurethane resin used for sofa leather and preparation process thereof | |
CN106674996A (en) | Self-repaired graphene oxide/polyurethane composite material and preparation method thereof | |
CN111909351A (en) | Synthetic method and application of waterborne polyurethane for microfiber impregnation | |
CN109354671B (en) | Preparation method of high-solid-content low-viscosity aqueous polyurethane emulsion | |
CN102558828A (en) | Method for preparing polyurethane hybridization material for hydroxyl-containing filler | |
CN102093703A (en) | Method for preparing chitin whisker modified waterborne polyurethane | |
CN103382253A (en) | Waterborne polyurethane dispersion with high performance and preparation method thereof | |
CN101235130A (en) | Cation water polyurethane emulsion and preparation method thereof | |
CN106700021A (en) | Chitosan modified cationic waterborne polyurethane resin and preparation method and application thereof | |
CN105732952B (en) | A kind of high-modulus non-ionic water polyurethane and preparation method thereof | |
CN115594839A (en) | Preparation method of citric acid modified aqueous polyurethane dispersion | |
CN107955123A (en) | The preparation method of the polyurethane-modified silicone oil of carbon fiber finish | |
CN108034225B (en) | Method for preparing chitosan/thermoplastic polyurethane elastomer composite material | |
CN111393596A (en) | Castor oil modified waterborne polyurethane nano-emulsion and preparation method thereof | |
CN115612120B (en) | Method for preparing novel aqueous polyurethane based on Pickering emulsion method | |
CN101280051A (en) | Method for preparing aromatic waterborne polyurethane from reproducible polylol | |
DE69838582T2 (en) | Improved process for the production of spherical polyurethane particles | |
KR20030038585A (en) | Synthesis of Silver/Polyurethane Nanocomposite Using Amphiphilic Urethane Acrylate | |
CN108752564B (en) | Synthetic method for preparing ZnO/nano-cellulose modified waterborne polyurethane by in-situ polymerization | |
CN112831011A (en) | Crosslinkable network-structure polyurethane emulsion and preparation method thereof | |
CN118063727B (en) | Water-based polyurethane resin modified by functional microsphere based on hydroxylated polystyrene and preparation method thereof | |
CN113061228A (en) | Preparation method of crosslinked polyurethane microspheres coated with carbon black particles, polyurethane microspheres and application thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
C17 | Cessation of patent right | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20080723 Termination date: 20100313 |