CN1326966C - Organic silicon modified polyurethane gap-filling rubber for cement road - Google Patents
Organic silicon modified polyurethane gap-filling rubber for cement road Download PDFInfo
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- CN1326966C CN1326966C CNB2004100357636A CN200410035763A CN1326966C CN 1326966 C CN1326966 C CN 1326966C CN B2004100357636 A CNB2004100357636 A CN B2004100357636A CN 200410035763 A CN200410035763 A CN 200410035763A CN 1326966 C CN1326966 C CN 1326966C
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Abstract
The present invention relates to organosilicon modified polyurethane gap filling rubber for a cement road. The organosilicon modified polyurethane gap filling rubber for a cement road of the present invention is prepared by the mixing reaction of a component A and a component B according to the proportion by weight of 1:1 to 2, wherein the component A is an organosilicon modified polyurethane prepolymer prepared by the copolymerization of polyether polyol, terminal hydroxyl organosilicon, isocyanate and a catalyst; the component B is prepared by the mix of an active hydrogen compound, a catalyst and a filler. The present invention overcomes the defects of the easy ageing, the easy viscosity losing, the poor elasticity and the poor fatigue resistance of the past gap filling rubber for a cement road surface. The present invention is a high-tech product having the advantages of high elasticity, high cohesiveness, ageing resistance and fatigue resistance. The present invention has the advantages of moderate price, excellent performance/price ratio and broad market prospects.
Description
(1) technical field under
The present invention relates to a kind of cement pavement gap-filling glue, particularly a kind of cement pavement is with the good organic silicon modified polyurethane gap-filling glue of resistance to deterioration.
(2) background technology
Facts have proved that the quality of cement pavement pointing is to guarantee the long-term normal important factor of using in concrete road surface.Good pointing can play watertight, airtight effect; and have elasticity, cohesiveness and favorable durability, weathering resistance, can stand seam crossing and expand with heat and contract with cold and stretch repeatedly, compress and be not destroyed, play the effect that long-term protection cement pavement seam crossing is not destroyed.
Polyurethane filling material is to be polymerized by active hydrogen compounds and isocyanate reaction, is divided into two kinds of single component and two-packs.The polyurethane molecular chain is soft segment and rigid chain segment bonded segmented copolymer.Contain in the molecular structure of polyurethane filling material-NCO and-strong polar group such as OH, reaction can form tough elastic bonding layer after solidifying.These constructional features, make polyurethane filling material have good elasticity and high adhesive property, and have characteristics such as oil resistant, wear-resisting, antifatigue, high-low temperature resistant, but the curing speed of isocyanate terminated polyurethane sealant is fast, curing can be released into out carbon dioxide when having water to exist, make glue-line bubble, cause defective.Simultaneously polyurethane filling material have a fatal weakness be exactly its weathering resistance not as organosilicon product, under secular sun lights, the cracking of hardening easily, significantly shorten work-ing life.
The organosilicon pointing has good thermotolerance, weathering resistance and electrical insulation capability, its the most outstanding advantage is exactly to have excellent ageing resistance and exclusive hydrophobicity performance, non-foaming, can with the firm bonding in non-porous material surface, the glue-line Heat stability is good is used it widely.But its anti-embedding degree and oil-proofness are relatively poor, the easy dialysis migration of material in the glue-line, and cost an arm and a leg.
(3) summary of the invention
The present invention is in order to overcome the deficiency of above technology, provide a kind of and urethane has been carried out the cement pavement gap-filling glue that the molecular structure modification is made by organosilicon, the shortcoming of both overcome that the urethane gap-filling glue is not weather-proof, the life-span is short has overcome again that the anti-embedding degree of organosilicon gap-filling glue is poor, oil-proofness difference and the high shortcoming of price.
The present invention realizes by following measure:
Cement pavement of the present invention is the two-pack pointing with the organic silicon modified polyurethane gap-filling glue, is to be made by 1: 1～2 weight ratio hybrid reaction by first component and second component; Described first component is to be 5～20 terminal hydroxy group polymethyl siloxane, the organopolysiloxane modified polyurethane prepolymer that isocyanic ester copolymerization under the effect of catalyzer Benzoyl chloride is made by polyether glycol, the polymerization degree; Described second component is to be mixed and made into by active hydrogen compounds, catalyzer dibutyl tin laurate and filler, and described active hydrogen compounds is 4,4 '-diamino-3, the mixture of 3 '-dichloro diphenyl methane and polyether glycol.
Gap-filling glue of the present invention, in the described second component, the weight ratio of described active hydrogen compounds and filler is 1: 2～7; Filler is one or more of talcum powder, light calcium carbonate, aerosil, calcium oxide, clorafin, pigment.
Gap-filling glue of the present invention, in the described first component, the weight ratio of polyether glycol, terminal hydroxy group polymethyl siloxane, isocyanic ester is 10: 1～4: 0.5～3.
Gap-filling glue of the present invention, in the described first component, the weight ratio of polyether glycol, terminal hydroxy group polymethyl siloxane, isocyanic ester is 10: 2～3: 1～2.
Gap-filling glue of the present invention, in the described first component, the hydroxyl value of polyether glycol is 20～120mgKOH/g, described isocyanic ester is a polyisocyanates.
1. gap-filling glue of the present invention, its principle is according to being:
The polyurethane high molecule material is to be the common high molecular materials of backbone structure with C-C (C-C) compound.C-C is that the kindliness of polyurethane high molecule of main chain is better, shows as snappiness.(347.5kJ/mol) is smaller in view of the bond energy between the C-C, and bond angle is narrow, therefore, nature chain rupture, degraded easily take place in its C-C main chain under natural ultraviolet long-term irradiation, stability is relatively poor relatively, therefore, polyurethane high molecule uses aging very fast under state of nature.This is an one deadly defect, generally speaking, if will prolong its work-ing life, just must add age inhibiting auxiliary agents such as ultraviolet absorption agent in the polyurethane high molecule material.Because these UV light absorber cost an arm and a leg, therefore can bring certain cost to raise to polyurethane material, simultaneously, the age inhibiting auxiliary agent that adds only is external cause and supplementary means, can not fundamentally all solve the problem of aging of urethane.
Organosilicon macromolecule be a kind of with silicon-oxygen (Si-O) key be main chain be different from the special construction macromolecular material that C-C is a main chain fully.Because the bond energy higher (422.5kJ/mol) of siloxane bond, the bond angle broad, therefore, the thermotolerance of organosilicon macromolecule, the polymer that resistance to deterioration is a main chain than general carbon-to-carbon singly-bound is good, and therefore worldwide, organosilicon material usually is used as the material that is sealing adhesive of outdoor weather-proof anti-irradiation, such as, glass curtain wall seal gum etc.But organosilicon material costs an arm and a leg mostly, and manufacturing technology is loaded down with trivial details, and Application Areas is subjected to certain limitation.
The organic silicon modified polyurethane technology is intended to the siloxane bond that ageing resistance is superior and is incorporated in the widely used cheap polyurethane high molecule chain, the advantage separately of two kinds of structural units of performance, thereby expectation fundamentally overcomes the weakness of conventional polyurethanes aging resistance of materials difference, reaches the purpose of structures shape performance.
The organosilicon segment enters in the polyurethane molecular chain, favorable durability, excellent adhesiveproperties is provided for urethane after the modification, and the modulus of polymkeric substance can height can be low, to adapt to different demands.
The polysiloxane segment enters in the polyurethane molecular chain, favorable durability, excellent adhesiveproperties is provided for urethane after the modification, and the modulus of polymkeric substance can height can be low, to adapt to different demands.
Because the introducing of siloxane bond, the organic silicon modified polyurethane gap-filling glue makes organic silicon modified polyurethane also have the characteristic of polysiloxane on the basis that has kept the every excellent properties of original urethane gap-filling glue.After the multipolymer film forming, the organosilicon segment is more prone to the surface enrichment orientation in the molecular structure, and the urethane segment is towards internal layer.This makes the mechanical properties such as sticking power, hardness, curing speed of co-polymer membrane improve, and the organosilicon low surface energy is maintained simultaneously.And the organic silicon modified polyurethane elastomerics also has better weathering resistance, resistance to deterioration and high thermal resistance, and this has just enlarged its Application Areas greatly.
Organic functions group on the organosilicon macromolecule chain plays an important role when reacting with the urethane intermediate and influences the performance of prepolymer.With the gap-filling glue of the urethane of organopolysiloxane modification preparation can such as improve stable ultraviolet resistance, weathering resistance, to the good balance of maintenance between directed application performances such as inorganic and cementability that organic substrate is excellent and its physicals.
With polysiloxane is soft section synthetic synthesis of polysiloxane-polyurethane block copolymer, excellent properties with polysiloxane and urethane, show good low temperature kindliness, dielectricity, surface enrichment and good biocompatibility etc., overcome the shortcoming of polysiloxane bad mechanical property, also remedied the deficiency of the weather-proof property of urethane difference, in aspect extensive application such as rubber, plastics, tackiness agent and coating, be a kind of very promising novel high polymer material.
The advantage of comprehensive above two kinds of materials, in cheap and good-quality polyurethane high molecule main chain, introduce part organosilicon macromolecule segment, thereby the backbone structure of polyurethane high molecule is carried out modification from the angle of molecular structure, the performances such as resistance to deterioration that fundamentally improve polyurethane material are practicable good thinkings, and be applied in the cement concrete pavement, have big novelty.
The terminal hydroxy group polymethyl siloxane carries out modification (first component) to urethane, and the chemical equation of reaction is as follows:
The organopolysiloxane modified polyurethane prepolymer forms final formation with the second component with polyurethane cross-linking agent by chemically crosslinked and has the cancellated polymkeric substance in space, and its structure as shown in the figure.
As seen from the figure, the urethane after the organopolysiloxane modification, crosslinked after, interconnect between the molecular chain, in the molecular chain and the reactive force between the molecular chain strengthen, aging ability such as the heat resistanceheat resistant light of this material strengthens.This proves absolutely to have only from structure and carry out modification, is only real modification completely.
2. a kind of preparation method of the present invention is as follows:
(1) first component preparation
1) polyether glycol, Benzoyl chloride and the hydroxyl-terminated injecting two methyl siloxane that measures added in the dry clean reactor.
2) under the vacuum tightness about-0.086MP, open stirring, open the water of condensation of condenser.Keep temperature of charge about 90 ℃, dewatered 2 hours.To condenser, during substantially anhydrous come out, close air intake valve, be cooled to 60 ℃.
3) add TDI and carry out prepolymerization reaction, stir down, temperature is at 40-60 ℃ in the controlling reactor, slowly add TDI, the strict controlled temperature of certain attention when adding TDI never can surpass 70 ℃ and (add the back and produce a large amount of heats, note control air inlet switch, should strict controlled temperature.Otherwise temperature is too high easily to cause implode).Stirred 30 minutes on the limit, and the limit slowly is warming up to 80-82 ℃, keeps this temperature range, polymerization under atmospheric pressure reaction 2 hours.Then, open vacuum system, under the vacuum tightness about-0.086MPa and 80 ± 2 ℃, the decompression dehydration reaction is 1-3 hour again.During to anhydrous come out, return to normal pressure gradually, close vacuum system at last.Be cooled to 50 ℃.Be discharged in airtight plastics or the metal bucket container sealed storage.Get the first component.
(2) preparation of second component
1) with talcum powder, light calcium carbonate, aerosil, calcium oxide, softening agent, catalyzer, antioxidant 1010, UV-327 UV light absorber, carbonization imines class hydrolysis stabilizer, MOCA, polyether glycol, pigment etc. mix under certain temperature condition, then with the sufficient dispersed with stirring of homogenizer, grind repeatedly with three-roll grinder again, stand-by.
2) scattered second component is poured in another reactor, under the 90 ℃ of left and right sides agitation conditions vacuum hydro-extraction 2-3 hour, poured into airtight storage in plastic containers or the iron ware then.Get the second component.
3. the performance test of pointing of the present invention
Get a certain amount of first component and second component, even by 1: 1.5 mixed, be applied in the various moulds, the self-vulcanizing moulding makes the organic silicon modified polyurethane pointing, carries out performance test.Its surface drying time is 3-10 hour, penetration degree is 2mm, elastic restoration ratio is 80%, tensile strength is 1.36Mpa, aging back draft intensity is 0.91Mpa, the maximum elongation rate is 911%, aging back maximum elongation rate is 775%, bonding strength is 0.380Mpa, aging back bonding strength is 0.350Mpa, and combustion initiation temperature is 260 degree, the influence of 80 ℃ of * 168 degree height, cement sheeting the cold drawn phenomenon of hot pressing can occur to the slit, in order to investigate the anti-fatigue performance of organic silicon modified polyurethane, experimental simulation true environment, 20 ℃ and-40 ℃ gap-filling glue has been done the cold drawn experiment of hot pressing respectively, find that gap-filling glue can also satisfy pavement displacement and be no more than 50% requirement 100% fully.It also has good anti-embedding degree and elastic restoration ratio, and the embedding that can resist sandstone fully, and its high temperature resistant, anti-immersion oil, corrosion-resistant are a kind of good pavement joint sealing materials.
In sum, cement pavement overcomes in the past with the organic silicon modified polyurethane gap-filling glue, and joint closure glue easily wears out, the shortcoming of easily inharmonious, poor flexibility, anti-fatigue ability difference, be a kind of snappiness, high-adhesion, anti-aging, fatigue proof high-tech product, and the result is moderate, have superior cost performance, have vast market prospect.
(4) description of drawings
Accompanying drawing is the netted structural representation in space of gap-filling glue of the present invention
(5) embodiment
Embodiment 1
(1) be that 2000 hydroxyl values are the polyoxypropyleneglycol of 54-58mgKOH/g with the 110g molecular weight, the 130g molecular weight is 3050, hydroxyl value is the polyoxytrimethylene triol of 54.5-57.5, and the 0.5g Benzoyl chloride and the 72g polymerization degree are that 5～7 hydroxyl-terminated injecting two methyl siloxane adds in the dry clean reactor.
(2) under the vacuum tightness about-0.086MP, open stirring, open the water of condensation of condenser.Keep temperature of charge about 90 ℃, dewatered 2 hours.To condenser, during substantially anhydrous come out, close air intake valve, be cooled to 60 ℃.
(3) add 56g TDI and carry out prepolymerization reaction, stir down, temperature is at 40-60 ℃ in the controlling reactor, slowly add TDI, the strict controlled temperature of certain attention when adding TDI never can surpass 70 ℃ and (add the back and produce a large amount of heats, note control air inlet switch, should strict controlled temperature.Otherwise temperature is too high easily to cause implode).Stirred 30 minutes on the limit, and the limit slowly is warming up to 80-82 ℃, keeps this temperature range, polymerization under atmospheric pressure reaction 2 hours.Then, open vacuum system, under the vacuum tightness about-0.086MPa and 80 ± 2 ℃, the decompression dehydration reaction is 1-3 hour again.During to anhydrous come out, return to normal pressure gradually, close vacuum system at last.Be cooled to 50 ℃.Be discharged in airtight plastics or the metal bucket container sealed storage.Get the first component.
(4) be that 2000 hydroxyl values are polyoxypropyleneglycol, the 2g dibutyl tin laurate of 54-58mgKOH/g with 16g MOCA, 100g molecular weight, and the following filler that amounts to 380g, talcum powder, light calcium carbonate, aerosil, calcium oxide, clorafin, antioxidant 1010, UV-327 UV light absorber, carbonization imines class hydrolysis stabilizer, pigment etc. mix under certain temperature condition, with the sufficient dispersed with stirring of homogenizer, grind repeatedly with three-roll grinder more then.Ground material is poured in another reactor, under the 90 ℃ of left and right sides agitation conditions vacuum hydro-extraction 2-3 hour, poured into airtight storage in plastic containers or the iron ware then.Get the second component.
When (5) using, first component and second component is even by 1: 1.5 mixed, be filled in the cement (cemented) joint.
Embodiment 2
(1) be that 4000 hydroxyl values are that polyoxypropyleneglycol, the 120g molecular weight of 26-30mgKOH/g is that 3000 hydroxyl values are that polyoxytrimethylene triol, 0.5g Benzoyl chloride and the 30g polymerization degree of 54-58mgKOH/g is that the hydroxyl-terminated injecting two methyl siloxane of 8-10 adds in the dry in advance clean reactor with the 150g molecular weight.
(2) under the vacuum tightness about-0.086MP, open stirring, open the water of condensation of condenser.Keep temperature of charge about 90 ℃, dewatered 2 hours.To condenser, during substantially anhydrous come out, close air intake valve, be cooled to 60 ℃.
(3) add 90g MDI and carry out prepolymerization reaction, under the stirring, temperature slowly adds MDI at 40-60 ℃ in the controlling reactor, and the strict controlled temperature of certain attention when adding MDI never can be above 70 ℃.Stirred 30 minutes on the limit, and the limit slowly is warming up to 80-82 ℃, keeps this temperature range, polymerization under atmospheric pressure reaction 2 hours.Then, open vacuum system, under the vacuum tightness about-0.086MPa and 80 ± 2 ℃, the decompression dehydration reaction is 1-3 hour again.During to anhydrous come out, return to normal pressure gradually, close vacuum system at last.Be cooled to 50 ℃.Be discharged in airtight plastics or the metal bucket container sealed storage.Get the first component.
(4) be that 4000 hydroxyl values are polyoxypropyleneglycol, the 2g dibutyl tin laurate of 26-30mgKOH/g with 16g MOCA, 160g molecular weight, and the following filler that amounts to 400g, talcum powder, light calcium carbonate, aerosil, calcium oxide, clorafin, antioxidant 1010, UV-327 UV light absorber, carbonization imines class hydrolysis stabilizer, Rutile type Titanium Dioxide, pigment etc. mix under certain temperature condition, with the sufficient dispersed with stirring of homogenizer, grind repeatedly with three-roll grinder more then.Ground material is poured in another reactor, under the 90 ℃ of left and right sides agitation conditions vacuum hydro-extraction 2-3 hour, poured into airtight storage in plastic containers or the iron ware then.Get the second component.
When (5) using, first, second component is even by 1: 1.5 mixed, be filled in the cement (cemented) joint.
Embodiment 3
(1) be that 1000 hydroxyl values are that polyoxypropyleneglycol, the 110g molecular weight of 105-117mgKOH/g is that 3050 hydroxyl values are that 51 polyoxytrimethylene triol, 0.5g Benzoyl chloride and the 48g polymerization degree are that the hydroxyl-terminated injecting two methyl siloxane of 11-13 adds in the dry clean reactor with the 61g molecular weight.
(2) under the vacuum tightness about-0.086MP, open stirring, open the water of condensation of condenser.Keep temperature of charge about 90 ℃, dewatered 2 hours.To condenser, during substantially anhydrous come out, close air intake valve, be cooled to 60 ℃.
(3) add 60g PAPI and carry out prepolymerization reaction, under the stirring, temperature slowly adds PAPI at 40-60 ℃ in the controlling reactor, and the strict controlled temperature of certain attention when adding PAPI never can be above 70 ℃.Stirred 30 minutes on the limit, and the limit slowly is warming up to 80-82 ℃, keeps this temperature range, polymerization under atmospheric pressure reaction 2 hours.Then, open vacuum system, under the vacuum tightness about-0.086MPa and 80 ± 2 ℃, the decompression dehydration reaction is 1-3 hour again.During to anhydrous come out, return to normal pressure gradually, close vacuum system at last.Be cooled to 50 ℃.Be discharged in airtight plastics or the metal bucket container sealed storage.Get the first component.
(4) be that 3050 hydroxyl values are 51 polyoxytrimethylene triol 2g dibutyl tin laurate with 12g MOCA, 120g molecular weight, and the following filler that amounts to 300g, talcum powder, light calcium carbonate, aerosil, calcium oxide, clorafin, antioxidant 1010, UV-327 UV light absorber, carbonization imines class hydrolysis stabilizer, Rutile type Titanium Dioxide, pigment etc. mix under certain temperature condition, with the sufficient dispersed with stirring of homogenizer, grind repeatedly with three-roll grinder more then.Ground material is poured in another reactor, under the 90 ℃ of left and right sides agitation conditions vacuum hydro-extraction 2-3 hour, poured into airtight storage in plastic containers or the iron ware then.Get the second component.
When (5) using, first, second component is even by 1: 1 mixed, be filled in the cement (cemented) joint.
Embodiment 4
(1) the 130g molecular weight is that 2000 hydroxyl values are that polypropylene oxide glycol, the 110g molecular weight of 50mgKOH/g is that 3050 hydroxyl values are that the hydroxyl-terminated injecting two methyl siloxane that 51 polyoxytrimethylene triol, 0.5g Benzoyl chloride and the 75g polymerization degree are adds in the dry clean reactor.
(2) under the vacuum tightness about-0.086MP, open stirring, open the water of condensation of condenser.Keep temperature of charge about 90 ℃, dewatered 2 hours.To condenser, during substantially anhydrous come out, close air intake valve, be cooled to 60 ℃.
(3) add 60g HDI and carry out prepolymerization reaction, stir down, temperature is at 40-60 ℃ in the controlling reactor, slowly add HDI, the strict controlled temperature of certain attention when adding HDI never can surpass 70 ℃ and (add the back and produce a large amount of heats, note control air inlet switch, should strict controlled temperature.Otherwise temperature is too high easily to cause implode).Stirred 30 minutes on the limit, and the limit slowly is warming up to 80-82 ℃, keeps this temperature range, polymerization under atmospheric pressure reaction 2 hours.Then, open vacuum system, under the vacuum tightness about-0.086MPa and 80 ± 2 ℃, the decompression dehydration reaction is 1-3 hour again.During to anhydrous come out, return to normal pressure gradually, close vacuum system at last.Be cooled to 50 ℃.Be discharged in airtight plastics or the metal bucket container sealed storage.Get the first component.
(4) be that 2000 hydroxyl values are polypropylene oxide glycol, the 2g dibutyl tin laurate of 50mgKOH/g with 18g MOCA, 80g molecular weight, and the following filler that amounts to 600g, talcum powder, light calcium carbonate, aerosil, calcium oxide, clorafin, antioxidant 1010, UV-327 UV light absorber, carbonization imines class hydrolysis stabilizer, Rutile type Titanium Dioxide, pigment etc. mix under certain temperature condition, with the sufficient dispersed with stirring of homogenizer, grind repeatedly with three-roll grinder more then.Ground thing carbonization imines class hydrolysis stabilizer, Rutile type Titanium Dioxide, pigment etc. are mixed under certain temperature condition,, grind repeatedly with three-roll grinder more then with the sufficient dispersed with stirring of homogenizer.Ground material is poured in another reactor, under the 90 ℃ of left and right sides agitation conditions vacuum hydro-extraction 2-3 hour, poured into airtight storage in plastic containers or the iron ware then.Get the second component.
When (5) using, first component and second component is even by 1: 2 mixed, be filled into the below of cement (cemented) joint, again the organosilicon pointing is filled to the top of cement (cemented) joint.
Pointing to the foregoing description has carried out performance test, and data are as follows.
| Maximum elongation rate % | Tensile strength Mpa | Cohesive strength MPa | Penetration degree mm | Hot pressing-cold drawn circulation | % behind the aging resistance | |
| Embodiment 1 | 911 | 1.36 | 0.38 | 1.5 | Can carry out at 100% time | Each property retention about 80% |
| Embodiment 2 | 950 | 1.32 | 0.35 | 2.0 | Can carry out at 100% time | Each property retention about 70% |
| Embodiment 3 | 750 | 1.51 | 0.42 | 1.3 | Can carry out at 100% time | Each property retention about 75% |
| Embodiment 4 | 1000 | 1.36 | 0.35 | 2.5 | Can carry out at 100% time | Each property retention about 80% |
Claims (5)
1. Modified polyurethane gap-filling adhesive of organosilicon for cement highway, it is characterized in that: this gap-filling glue is to be made by 1: 1～2 weight ratio hybrid reaction by first component and second component;
Described first component is to be 5～20 terminal hydroxy group polymethyl siloxane, the organopolysiloxane modified polyurethane prepolymer that isocyanic ester copolymerization under the effect of catalyzer Benzoyl chloride is made by polyether glycol, the polymerization degree;
Described second component is to be mixed and made into by active hydrogen compounds, catalyzer dibutyl tin laurate and filler, and described active hydrogen compounds is 4,4 '-diamino-3, the mixture of 3 '-dichloro diphenyl methane and polyether glycol.
2. Modified polyurethane gap-filling adhesive of organosilicon for cement highway according to claim 1 is characterized in that: in the described second component, the weight ratio of described active hydrogen compounds and filler is 1: 2～7; Filler is one or more of talcum powder, light calcium carbonate, aerosil, calcium oxide, clorafin, pigment.
3. Modified polyurethane gap-filling adhesive of organosilicon for cement highway according to claim 1 is characterized in that: in the described first component, the weight ratio of polyether glycol, terminal hydroxy group polymethyl siloxane, isocyanic ester is 10: 1～4: 0.5～3.
4. Modified polyurethane gap-filling adhesive of organosilicon for cement highway according to claim 3 is characterized in that: in the described first component, the weight ratio of polyether glycol, terminal hydroxy group polymethyl siloxane, isocyanic ester is 10: 2～3: 1～2.
5. Modified polyurethane gap-filling adhesive of organosilicon for cement highway according to claim 3 is characterized in that: in the described first component, the hydroxyl value of polyether glycol is 20～120mgKOH/g, and described isocyanic ester is a polyisocyanates.
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| Application Number | Priority Date | Filing Date | Title |
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| CNB2004100357636A CN1326966C (en) | 2004-09-21 | 2004-09-21 | Organic silicon modified polyurethane gap-filling rubber for cement road |
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| CNB2004100357636A CN1326966C (en) | 2004-09-21 | 2004-09-21 | Organic silicon modified polyurethane gap-filling rubber for cement road |
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| CN1326966C true CN1326966C (en) | 2007-07-18 |
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| CN1616577A (en) | 2005-05-18 |
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