CN101412801A - Polyurethane slurry for hasp and preparation thereof - Google Patents
Polyurethane slurry for hasp and preparation thereof Download PDFInfo
- Publication number
- CN101412801A CN101412801A CNA2008101597315A CN200810159731A CN101412801A CN 101412801 A CN101412801 A CN 101412801A CN A2008101597315 A CNA2008101597315 A CN A2008101597315A CN 200810159731 A CN200810159731 A CN 200810159731A CN 101412801 A CN101412801 A CN 101412801A
- Authority
- CN
- China
- Prior art keywords
- polyurethane slurry
- preparation
- hasp
- solvent
- hasp according
- 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.)
- Granted
Links
Landscapes
- Polyurethanes Or Polyureas (AREA)
Abstract
The invention discloses polyurethane slurry for an agraffe and a preparation method thereof. The polyurethane slurry for the agraffe is formed by chemical combination of 0.2 to 0.25 portion of polyester multi-alcohol with molecular weight of between 1,800 and 2,200, 0.26 to 0.96 portion of terylene ethylene glycol, 0 to 0.11 portion of 1.4 butanediol or 1.3 butanediol, 0 to 0.007 portion of trimethylolpropane and 0.065 to 1.2 portions of toluene diisocynate. The polyurethane slurry for the agraffe has the characteristics of short curing time, high tensile strength, strong water resisting property and alkaline cleaning resistance, environmental protection, tough and straight hand feeling and high color preserving degree.
Description
Technical field
The invention belongs to chemical technology field, especially relate to special-purpose polyurethane slurry of a kind of velcro and preparation method thereof.
Background technology
The special-purpose polyurethane slurry of velcro generally all is to adopt two component conventional polyurethanes tackiness agent, promptly 101 glue substitute, need solidify 24 hours at 45 ℃ ± 1 ℃ thermostatic chamber, could carry out aftertreatment-itemize to hasp, scrape button, because set time is long, the conditional request harshness, cause the technical process of production hasp producer long, power consumption is big, efficient is low, cost is low, not environmental protection, does not reach export standard, is eliminated gradually.
Summary of the invention
The objective of the invention is to improve the deficiency of prior art and provide a kind of set time short, tensile strength is high, water-fastly, alkaline-resisting wash that performance is strong, tough and tensile straight and upright, the special-purpose polyurethane slurry of velcro that the fresh-keeping degree of color and luster is high of environmental protection, feel and preparation method thereof.
The object of the present invention is achieved like this, a kind of polyurethane slurry for hasp, and the general molecular formula of this polyurethane slurry is:
R is not for containing the alkyl of aromatic proton in the formula.
A kind of preparation method of above-mentioned polyurethane slurry, be characterized in that this method is is that 0.2-0.25 part molecular weight is 2000 ± 200 polyester polyol by equivalent part, 0.26-0.96 part of terylene level ethylene glycol, 0-0.11 part 1.4 butyleneglycols or 1.3 butyleneglycols, 0-0.007 part TriMethylolPropane(TMP), 0.625-1.2 parts tolylene diisocyanate chemical combination forms.
Be with in bottoming solvent, other reactants input reactors except that tolylene diisocyanate, stir, sealing then, be warming up to 60-65 ℃, slowly drip tolylene diisocyanate, titration in 2-3 hour, 70-90 ℃ of insulation reaction added catalyzer after 3 hours, reacted 40-120 minute again, cooling adds letdown solvent dun, stir, with being coated with 4# cup viscosimetric 30-80S under 25 ℃ of temperature, qualified back adds additive, get the material package dress at 35-40 ℃, bottoming solvent and letdown solvent dun are collectively referred to as total solvent.
The bottoming solvent is made up of grade oil toluene that accounts for total solvent 2%-20% and 4%-15% the N.N dimethyl formamide that accounts for total solvent.
Letdown solvent dun is by N, N dimethyl formamide, N, N N,N-DIMETHYLACETAMIDE, pimelinketone, butanone, three kinds and above mixing in acetone, toluene, dimethylbenzene, vinyl acetic monomer, N-BUTYL ACETATE, the methylal.
Catalyzer is can be a kind of or any mixing in organotin, the organic amine.。
Catalyzer can be 4-methyl hexamethylene diamine, Tetramethyl Ethylene Diamine, compound tertiary amine, triethylene diamine, N-methylmorpholine, 1.4-dimethyl benzylamine, the 4-methyl-diaminopropane in the stannous octoate, dibutyl tin laurate, organic amine in the organotin.
Additive is that in the glycols of V-6 fire retardant, composite flame-retardant agent, fire-retardant silicone oil L-570, L-620, low-carbon (LC) one or more are mixed.
When adding additive, add stablizer.
Stablizer is one or more mixing in the ultraviolet (UV) of anti-xanthochromia the-R, UV326/327, high-efficiency anti-oxidant 1008C, the phosphoric acid ester.
Compared with the prior art the present invention has following distinguishing feature and positively effect: the present invention adopts polyester polyol, terylene level ethylene glycol, 1.4 butyleneglycols, tolylene diisocyanate, TriMethylolPropane(TMP) reaction to synthesize, and can get the different length molecular chain of different end group polymkeric substance down in different mol ratio (or equivalent):
(2)-----end group contains-OH
(1)+(2) or other polyol further react and generate high molecular urethane resin.For example:
In the structural formula R for the alkyl that does not contain aromatic proton adds by a certain percentage again low charcoal dibasic alcohol, as chain extension again just such as ethylene glycol, propylene glycol, 1.3 butyleneglycols, 1.4 butyleneglycols, neopentyl glycol, forms higher high molecular polymer or than hanging down superpolymer.The present invention utilizes this reaction rule exactly, in conjunction with the velcro performance requriements, the common polyurethane resin structure is carried out modification, makes in its urethane resin structure soft section and a hard section chain link be suitable for the velcro performance requriements and designs.
So-called soft section be by the polyester polyol of molecular weight 2000 ± 200 and polyisocyanates-the NCO radical reaction forms, hard section then is by low-carbon (LC) dibasic alcohol and di-isocyanate reaction generation.
Embodiment
Embodiment 1, and a kind of polyurethane slurry for hasp is that the general molecular formula of this polyurethane slurry is:
R is not for containing the alkyl of aromatic proton in the formula, be to form in the bottoming solvent input reactor by the grade oil toluene of 79Kg and the N.N dimethyl formamide of 40Kg, be molecular weight 2100 polyester polyol 146Kg again, terylene level ethylene glycol 20.7Kg, disposable input, stir, sealing then, be warming up to 60-65 ℃, slowly drip the 70Kg tolylene diisocyanate, titration in 2-3 hour, 70-90 ℃ of insulation reaction is after 3 hours, add catalyzer 4-methyl hexamethylene diamine and N-methylmorpholine, react 40-50 minute viscosity again and reach set quota, stopped reaction, cooling adds the vinyl acetic monomer by 304Kg, the letdown solvent dun that the acetone of 179Kg and the toluene of 90Kg are formed, stir, with being coated with 4# cup viscosimetric 30-80S under 25 ℃ of temperature, 1.4 butyleneglycols in the glycols of qualified back adding additive low-carbon (LC) are got the material package dress at 35-40 ℃.
Embodiment 2, and a kind of polyurethane slurry for hasp is that the general molecular formula of this polyurethane slurry is:
R is not for containing the alkyl of aromatic proton in the formula, be to form in the bottoming solvent input reactor by the grade oil toluene of 81Kg and the N.N dimethyl formamide of 44Kg, be molecular weight 2000 polyester polyol 184Kg again, terylene level ethylene glycol 13.8Kg, 1.3 the disposable input of butyleneglycol 2.8Kg, stir, sealing then, be warming up to 60-65 ℃, slowly drip the 60.2Kg tolylene diisocyanate, titration in 2-3 hour, 70-90 ℃ of insulation reaction is after 3 hours, add the inferior tin of octoate catalyst, 1.4-dimethyl benzylamine and 4-methyl-diaminopropane react 40-50 minute viscosity again and reach set quota, stopped reaction, cooling adds the N by 280Kg, the N N,N-DIMETHYLACETAMIDE, the cyclohexanone of 98Kg, the letdown solvent dun that the N-BUTYL ACETATE of 324Kg is formed stirs, with being coated with 4# cup viscosimetric 30-80S under 25 ℃ of temperature, qualified back adds by V-6 fire retardant, additive that composite flame-retardant agent and fire-retardant silicone oil L-570 form and the triphenyl phosphite in the stablizer phosphoric acid ester are got the material package dress at 35-40 ℃.
Embodiment 3, and a kind of polyurethane slurry for hasp is that the general molecular formula of this polyurethane slurry is:
R is not for containing the alkyl of aromatic proton in the formula, be to form in the bottoming solvent input reactor by the grade oil toluene of 44Kg and the N.N dimethyl formamide of 22Kg, be molecular weight 1800 polyester polyol 100Kg again, terylene level ethylene glycol 7.3Kg, the disposable input of TriMethylolPropane(TMP) 0.15Kg, stir, sealing then, be warming up to 60-65 ℃, slowly drip the 30.4Kg tolylene diisocyanate, titration in 2-3 hour, 70-90 ℃ of insulation reaction is after 3 hours, add the inferior tin of octoate catalyst, react 40-50 minute viscosity again and reach set quota, stopped reaction, cooling adds the N by 98Kg, the N dimethyl formamide, the methylal of 149Kg, the dimethylbenzene of 50Kg, the letdown solvent dun that the acetone of 50Kg is formed stirs, with being coated with 4# cup viscosimetric 30-80S under 25 ℃ of temperature, the stablizer that qualified back adds additive V-6 fire retardant and is made up of high-efficiency anti-oxidant 1008C and the ultraviolet (UV) of anti-xanthochromia the-R is got the material package dress at 35-40 ℃.
Embodiment 4, and a kind of polyurethane slurry for hasp is that the general molecular formula of this polyurethane slurry is:
R is not for containing the alkyl of aromatic proton in the formula, be to form in the bottoming solvent input reactor by the grade oil toluene of 79Kg and the N.N dimethyl formamide of 40Kg, be molecular weight 2100 polyester polyol 146Kg again, terylene level ethylene glycol 19.5Kg, 1.4 butyleneglycol 1.5Kg, the disposable input of TriMethylolPropane(TMP) 0.26Kg, stir, sealing then, be warming up to 60-65 ℃, slowly drip the 70Kg tolylene diisocyanate, titration in 2-3 hour, 70-90 ℃ of insulation reaction is after 3 hours, add the inferior tin of octoate catalyst, react 40-50 minute viscosity again and reach set quota, stopped reaction, cooling adds the N by 106Kg, the N dimethyl formamide, the butanone of 89Kg, the letdown solvent dun that the grade oil toluene of 446Kg is formed stirs, with being coated with 4# cup viscosimetric 30-80S under 25 ℃ of temperature, the stablizer that qualified back adds additive V-6 fire retardant and is made up of high-efficiency anti-oxidant 1008C and the ultraviolet (UV) of anti-xanthochromia the-R is got the material package dress at 35-40 ℃.
Embodiment 5, and a kind of polyurethane slurry for hasp is that the general molecular formula of this polyurethane slurry is:
R is not for containing the alkyl of aromatic proton in the formula, be to form in the bottoming solvent input reactor by the grade oil toluene of 81Kg and the N.N N,N-DIMETHYLACETAMIDE of 41Kg, be molecular weight 1900 polyester polyol 184Kg again, terylene level ethylene glycol 13.5Kg, 1.3 butyleneglycol 2.5Kg, the disposable input of TriMethylolPropane(TMP) 0.26Kg, stir, sealing then, be warming up to 60-65 ℃, slowly drip the 60Kg tolylene diisocyanate, titration in 2-3 hour, 70-90 ℃ of insulation reaction is after 3 hours, add the catalyzer Tetramethyl Ethylene Diamine, react 40-50 minute viscosity again and reach set quota, stopped reaction, cooling adds the N by 82Kg, the N N,N-DIMETHYLACETAMIDE, the pimelinketone of 89Kg, the letdown solvent dun that the grade oil toluene of 468Kg is formed stirs, with being coated with 4# cup viscosimetric 30-80S under 25 ℃ of temperature, qualified back adds the fire-retardant silicone oil L-570 of additive, by the stablizer that the dimethyl phosphate of ultraviolet (UV) of anti-xanthochromia the 326/327 and phosphoric acid ester is formed, get the material package dress at 35-40 ℃.
Example 6, a kind of polyurethane slurry for hasp is that the general molecular formula of this polyurethane slurry is:
R is not for containing the alkyl of aromatic proton in the formula, be to be 2000 polyester polyol 100kg and terylene level ethylene glycol 7.3kg with molecular weight, 1.4 butyleneglycol 1.4kg, the disposable input of TriMethylolPropane(TMP) 0.15kg, add the bottoming solvent of forming by toluene 44kg and 22kg N.N solvent dimethylformamide again, stir, then sealing, heat up 60-65 ℃, slowly drip the 32.2kg tolylene diisocyanate, dripped off in 2-3 hours, 80-85 ℃ of insulation reaction 3 hours, add the catalyzer dibutyl tin laurate, reacted 40-50 minutes, viscosity reaches set quota again, the cooling stopped reaction, add by pimelinketone 45kg, N, N dimethyl formamide 48kg, the letdown solvent dun that petroleum toluene 254kg forms, stir, with being coated with 4# cup viscosimetric 30-80S under 25 ℃ of temperature, qualified after, add the fire-retardant silicone oil L-620 of additive, the stablizer ultraviolet (UV) of anti-xanthochromia the-326/327 is got the material package dress at 35-40 ℃.
The present invention is a thermoplastically two liquid type polyurethane resin, form tough and tensile film as the special-purpose sizing agent of pull stap, this product is that to add water decomposition, photostabilization, anti-swelling deformability, pigment color emissivity superior, and outward appearance is water white transparency or little yellow liquid, Sn<0.1ppm in this product, As<0.01ppm, Pb<0.02ppm, Cd<0.05ppm, Cr<0.01ppm, Hg<0.002ppm does not contain organic aldehyde and polychlorobiphenyl and azo-compound.
Claims (10)
2, the preparation method of the described polyurethane slurry for hasp of a kind of claim 1, it is characterized in that this method is is that 0.2-0.25 part molecular weight is 2000 ± 200 polyester polyol by equivalent part, 0.26-0.96 part of terylene level ethylene glycol, 0-0.11 part 1.4 butyleneglycols or 1.3 butyleneglycols, 0-0.007 part TriMethylolPropane(TMP), 0.625-1.2 parts tolylene diisocyanate chemical combination forms.
3, the preparation method of a kind of polyurethane slurry for hasp according to claim 2, it is characterized in that this method is with the bottoming solvent, other reactants except that tolylene diisocyanate drop in the reactor, stir, sealing then, be warming up to 60-65 ℃, slowly drip tolylene diisocyanate, titration in 2-3 hour, 70-90 ℃ of insulation reaction is after 3 hours, add catalyzer, reacted 40-120 minute, cooling adds letdown solvent dun, stirs again, with being coated with 4# cup viscosimetric 30-80S under 25 ℃ of temperature, qualified back adds additive, gets the material package dress at 35-40 ℃, and bottoming solvent and letdown solvent dun are collectively referred to as total solvent.
4, the preparation method of a kind of polyurethane slurry for hasp according to claim 3 is characterized in that described bottoming solvent is made up of grade oil toluene that accounts for total solvent 2%-20% and 4%-15% the N.N dimethyl formamide that accounts for total solvent.
5, the preparation method of a kind of polyurethane slurry for hasp according to claim 3, it is characterized in that described letdown solvent dun is by N, N dimethyl formamide, N, the N N,N-DIMETHYLACETAMIDE, pimelinketone, butanone, three kinds and above mixing in acetone, toluene, dimethylbenzene, vinyl acetic monomer, N-BUTYL ACETATE, the methylal.
6, the preparation method of a kind of polyurethane slurry for hasp according to claim 3 is characterized in that described catalyzer is can be a kind of or any mixing in organotin, the organic amine.
7, the preparation method of a kind of polyurethane slurry for hasp according to claim 6 is characterized in that described catalyzer can be 4-methyl hexamethylene diamine, Tetramethyl Ethylene Diamine, compound tertiary amine, triethylene diamine, N-methylmorpholine, 1.4-dimethyl benzylamine, the 4-methyl-diaminopropane in the stannous octoate, dibutyl tin laurate, organic amine in the organotin.
8, the preparation method of a kind of polyurethane slurry for hasp according to claim 3 is characterized in that described additive is that in the glycols of V-6 fire retardant, composite flame-retardant agent, fire-retardant silicone oil L-570, fire-retardant silicone oil L-620, low-carbon (LC) one or more are mixed.
9, the preparation method of a kind of polyurethane slurry for hasp according to claim 3 is characterized in that adding stablizer when adding additive.
10, the preparation method of a kind of polyurethane slurry for hasp according to claim 9 is characterized in that described stablizer is one or more mixing in the ultraviolet (UV) of anti-xanthochromia the-R, the ultraviolet (UV) of anti-xanthochromia the 326/327, high-efficiency anti-oxidant 1008C, the phosphoric acid ester.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2008101597315A CN101412801B (en) | 2008-11-06 | 2008-11-06 | Polyurethane slurry for hasp and preparation thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2008101597315A CN101412801B (en) | 2008-11-06 | 2008-11-06 | Polyurethane slurry for hasp and preparation thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
CN101412801A true CN101412801A (en) | 2009-04-22 |
CN101412801B CN101412801B (en) | 2010-12-29 |
Family
ID=40593555
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2008101597315A Active CN101412801B (en) | 2008-11-06 | 2008-11-06 | Polyurethane slurry for hasp and preparation thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN101412801B (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102443131A (en) * | 2011-09-19 | 2012-05-09 | 烟台市福山区化学工业研究所有限公司 | Non-yellowing polyurethane slurry for hasp, and preparation method thereof |
CN111718468A (en) * | 2020-07-15 | 2020-09-29 | 烟台云泷化学制品有限公司 | Low-cost high-hardness polyurethane stiffening agent slurry and preparation method and application thereof |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1048720A (en) * | 1989-07-13 | 1991-01-23 | 烟台市福山区化学工业研究所 | Polyurethane binder |
-
2008
- 2008-11-06 CN CN2008101597315A patent/CN101412801B/en active Active
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102443131A (en) * | 2011-09-19 | 2012-05-09 | 烟台市福山区化学工业研究所有限公司 | Non-yellowing polyurethane slurry for hasp, and preparation method thereof |
CN111718468A (en) * | 2020-07-15 | 2020-09-29 | 烟台云泷化学制品有限公司 | Low-cost high-hardness polyurethane stiffening agent slurry and preparation method and application thereof |
Also Published As
Publication number | Publication date |
---|---|
CN101412801B (en) | 2010-12-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101597470B (en) | Solvent free bi-component polyurethane adhesive and preparation method thereof | |
CN103183806B (en) | A kind of High-flame-retardanthard hard polyurethane foam and preparation method thereof | |
CN105295702B (en) | Elastic coating and preparation method thereof | |
CN106554612B (en) | Halogen-free fire retardation thermoplastic polyurethane elastic composition and its product, fire retardant packet | |
CN109134802B (en) | Phosphorus-containing halogen-free flame-retardant thermoplastic polyurethane elastomer composition and preparation method and application thereof | |
CN106010415B (en) | A kind of full water foamed cold-curing foam fireproof gap-filling glue and preparation method thereof | |
CN108753243B (en) | Multi-component polyurethane pouring sealant and preparation method thereof | |
JP2010539264A5 (en) | Coating composition and method for curing it | |
JPS59105024A (en) | Manufacture of aromatic polyol mixture and manufacture of hard polyurethane foam and polyisocyanurate foam | |
CN107722908A (en) | A kind of preparation method of polyurethane fireproof glue for building | |
CN107459620A (en) | The preparation method of flame-proof polyol and its polyurethane foam of preparation and polyurethane sealant | |
EP1362873A1 (en) | Powder coatings based on polyesters and thermoset modified polyesters | |
CN108456483A (en) | A kind of one pack system water proof fire retardant polyurethane coating | |
CN103820016B (en) | A kind of polycarbonate polyurethane priming paint and preparation method thereof | |
CN105885704A (en) | Low-viscosity high-strength environmentally friendly double-component glue solution and preparation method thereof | |
CA3102994A1 (en) | Lignin-based polyurethane prepolymers, polymers, related compositions, and related methods | |
CN102127199A (en) | Diisocyanate prepolymer as curing agent and preparation method thereof | |
CN110511714A (en) | Polyurethane fireproof glue for building | |
CN101412801B (en) | Polyurethane slurry for hasp and preparation thereof | |
JP6226549B2 (en) | Terminal hydroxyl group-containing resin composition and production method thereof, crosslinkable coating composition, coating film, and article | |
CN101514269A (en) | Dicyclohexylmethylmethane-4,4'-diisocyanate prepolymer used for paint curing agent and preparation method thereof | |
CN101503595B (en) | Yellowing-resistant solvent type polyurethane leather coating agent and preparation thereof | |
EP3288993B1 (en) | Polyurethane outer shells having reduced water absorption and their use | |
EP3805228A1 (en) | A method for preparation of an isosorbide-based photocurable composition | |
CN104262575B (en) | A kind of phosphate-based epoxy modified aqueous polyurethane and preparation method 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 |