CN109097998A - A kind of waterproof roll and preparation method thereof - Google Patents
A kind of waterproof roll and preparation method thereof Download PDFInfo
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Abstract
The invention discloses a kind of waterproof rolls and preparation method thereof, belong to architectural waterproof material technical field.The present invention forms compounding with polytetramethylene ether glycol, polycaprolactone, forms polyol systems, forms flexible polyurethanes high polymer, improve intensity, the adhesiveness of pitch, can form buffering, increase the wear-resisting property of coiled material;The present invention carries out esterification using trimellitic anhydride, diisopropanol as raw material, asphaltene molecule can be made to be fixed in three-dimensional structure, so that the ability of anti-foreign matter insertion is enhanced, waterproof resistance is improved;Magnesium nitrate, aluminum nitrate is added in the present invention, adds urea, carries out the inhibition and suspension of oxidation reaction, forms synergistic effect, and the infiltration of resisting chloride ion penetration reduces corrosion, plays preferable protective effect to the ageing-resistant performance of waterproof roll.Present invention understands that current waterproof roll of having determined is weather-proof, loss of properties on aging, the problem of poor mechanical property.
Description
Technical field
The invention belongs to architectural waterproof material technical fields, and in particular to a kind of waterproof roll and preparation method thereof.
Background technique
With the development of economy with the progress in epoch, the requirement to construction material is higher and higher, and original construction material is
It is not able to satisfy the demand of era development.Many buildings are all to reduce service life because of the erosion of water.With people couple
The requirement of building service life is higher and higher, and requirement of the people to waterproof material quality is increasingly paid attention to.Waterproof roll is to build
Build common a kind of construction material in construction, road and bridge, roof or need waterproof the construction of building in, be required to pre-
First paved waterproof roll.In the production process of waterproof roll, the adhesion of waterproof roll will use isolation film in order to prevent, in order to make
Isolation film and waterproof roll can be bonded together, it will usually first its surface be laid with cementing layer, isolated material by cementing layer with
Waterproof material combines, and reaches isolation effect.The most commonly used is PET(polyester) film, on the one hand, waterproof roll must in construction
Isolated material must be removed before casting concrete, and the isolation film removed can not be used again, and both increases apply in this way
Workload, also not environmentally;On the other hand, cementing layer is easy aging, will affect the combination effect of waterproof layer and concrete, is unfavorable for
The holding of waterproof effect, and in the construction process, as isolation film is stripped, exposed cementing layer can glue foot, influence construction effect
Rate.
There is a kind of adhesive waterproof coil in the market, but coiled material mainly includes waterproof substrate and self-adhesive layer, is equivalent in tradition
Self-adhesive layer is additionally arranged on the basis of coiled material.Although combined type self-adhesive waterproof roll material solves the problems, such as that construction is difficult, but layer and layer
Between compatibility, the croop property of waterproof substrate be still an important factor for limiting its performance.In contrast, by tack waterproof
Material, which is directly coated on, to be made waterproof roll on tire base and seems advantageously.At present also disclose one kind by asphalt, subtract
Third fractional oil, thermoplastic styrene butadiene rubber, powder styrene butadiene rubber, coumarone indene resin, Petropols, terpene resin, small-molecular-weight gather different
Butylene, ultraviolet absorbing agent, antioxidant, the production of bitumen layer made of calcium carbonate waterproof roll.The waterproof roll uses SBR fourth
The preparation of benzene rubber rubber powder, the waterproof roll sizing material is there are loss of properties on aging, the disadvantages of non-refractory.Therefore a kind of property need to be developed
The good waterproof roll of energy.
Summary of the invention
The technical problems to be solved by the invention: weather-proof, loss of properties on aging, poor mechanical property for current waterproof roll
The problem of, a kind of waterproof roll and preparation method thereof is provided.
In order to solve the above technical problems, the present invention is using technical solution as described below:
A kind of waterproof roll, including elastomer additives, modifying agent, uvioresistant absorbing additives, antioxidant;
The preparation method of the elastomer additives, includes the following steps:
(1) it takes polytetramethylene ether glycol 2 ~ 5:1 in mass ratio ~ 4 that polycaprolactone is added, is warming up to 80 ~ 85 DEG C and is stirred,
Mixture is obtained, takes mixture 10 ~ 20:1 in mass ratio ~ 3 that dimethylbenzene mixing is added, is cooled to 50 ~ 60 DEG C, polytetramethylene is added
The toluene di-isocyanate(TDI) that 2 ~ 4 times of ether quality of glycol is stirred, and must stir mixture a;
(2) it takes three (2- ethoxy) isocyanuric acid ester 2 ~ 5:2 in mass ratio ~ 6 that triisopropanolamine is added, is warming up to 85 ~ 90 DEG C and stirs
Mixing is mixed, mixture a is obtained, takes stirring mixture a 10 ~ 15:2 in mass ratio ~ 5 that mixture a is added, adds stirring mixture a
The dibutyl tin dilaurate of quality 1 ~ 5% is stirred in 80 ~ 85 DEG C, is cooled to room temperature to get elastomer additives.
Stirring mixture a's is stirred condition in the step (1) are as follows: is warming up to 75 ~ 80 DEG C and is stirred 1 ~ 3h.
The preparation method of the modifying agent, includes the following steps:
S1. it takes trimellitic anhydride 1 ~ 3:10 in mass ratio ~ 20 that n,N-dimethylacetamide is added, is stirred in 45 ~ 55 DEG C,
Mixed liquor a is obtained, takes diisopropanol 2 ~ 4:10 in mass ratio ~ 15 that n,N-dimethylacetamide is added, 30 ~ 50min of magnetic agitation is obtained
Mixed liquor b takes 3 ~ 6:3 ~ 5 in mass ratio mixed liquor a to be added dropwise in mixed liquor b, controls 30 ~ 50min of time for adding, is passed through nitrogen
Protection, is stirred in 25 ~ 30 DEG C, obtains stirring mixture;
S2. take stirring mixture 80 ~ 90:6 in mass ratio ~ 9 that triethanolamine is added, addition is stirred amount of substance 0.5 ~ 1.5%
P-methyl benzenesulfonic acid is passed through nitrogen protection, adds the toluene for being stirred amount of substance 30 ~ 50%, is warming up to 130 ~ 135 DEG C of stirrings
Mixing, is cooled to room temperature, and is evaporated under reduced pressure, obtains vacuum distillation object, and vacuum distillation object 20 ~ 30:1 in mass ratio ~ 4:0.1 ~ 0.3 is taken to add
Enter methyl acrylate, hydroquinone, adds the p-methyl benzenesulfonic acid of vacuum distillation amount of substance 1 ~ 4%, be warming up to 90 ~ 95 DEG C of stirrings
10 ~ 12h is mixed, is evaporated under reduced pressure to get modifying agent.
The preparation method of the uvioresistant absorbing additives, includes the following steps:
It takes magnesium nitrate 3 ~ 6:1 in mass ratio ~ 3:15 ~ 20 that aluminum nitrate, absolute ethyl alcohol and stirring mixing is added, adds dehydrated alcohol matter
The urea of amount 50 ~ 60%, ultrasonic disperse are stirred in 140 ~ 150 DEG C, are cooled to room temperature, and are centrifuged, and take precipitating through deionized water
Washing, it is dry, it grinds and sieves with 100 mesh sieve, collect sieving particle to get uvioresistant absorbing additives.
The antioxidant are as follows: take β-(4- hydroxy phenyl -3,5- di-t-butyl) propionic acid n-octadecyl alcohol ester in mass ratio 1 ~
4:3 ~ 6 be added (2, the 4- di-tert-butyl-phenyl) ester of phosphorous acid three mixing to get.
A kind of preparation method of waterproof roll, the preparation method include the following steps:
A. according to the mass fraction, take 100# asphalt heating to be stirred to 170 ~ 180 DEG C, 100# asphalt quality 20 ~ 50% is added
The mixing of 10# asphalt mixing, adds the elastomer additives of 100# asphalt quality 20 ~ 40%, is stirred, obtains in 100 ~ 120 DEG C
Matrix object;
B. as mass fraction, 8 ~ 12 parts of modifying agent, 5 ~ 8 parts of uvioresistant absorbing additives, 1 ~ 4 part of antioxidant, 20 ~ 30 parts of cunnings are taken
Mountain flour is stirred in 75 ~ 80 DEG C, obtains mixture b, takes mixture b 3 ~ 5:10 in mass ratio ~ 30 that the stirring of matrix object is added mixed
It closes, obtains maceration extract, polyester felt is taken to immerse maceration extract, keep 3 ~ 5min, take out polyester felt tabletting after dipping, it is dry to get anti-roll
Material.
Maceration extract is stirred condition in the step B are as follows: is stirred 40 ~ 50min in 170 ~ 180 DEG C.
The present invention is compared with other methods, and advantageous effects are:
(1) present invention forms compounding with polytetramethylene ether glycol, polycaprolactone, forms polyol systems, and it is more to introduce polyethers
First alcohol, increases the performance of weather-proof, the water-fast and resistance to mildew of elastomer additives, polyester polyol can improve material oil resistant and
Mechanical property adds toluene di-isocyanate(TDI), through three (2- ethoxy) isocyanuric acid esters, triisopropanolamine mixing chain extension, shape
At flexible polyurethanes high polymer, the addition of mixed chain extender improves the crosslink density of elastomer, reduces hydrogen bond ratio
Example improves thermal stability, high temperature resistant isocyanurate ring is introduced in polyurethane structural, and poly- by alternating temperature after cure increase
The content of urethane elastomer internal chemical cross-linked structure, improves high temperature resistance, while the addition of elastomer enters pitch body
After system, distribute raw swelling action with saturation point and fragrance, by absorbing the small molecules objects such as the saturation point in pitch, fragrance point
Matter increases macromolecular and polar substances in whole system, improves intensity, the adhesiveness of pitch, can form buffering, increases
The wear-resisting property of coiled material;
(2) present invention is that raw material carries out esterification using trimellitic anhydride, diisopropanol, addition triethanolamine as core molecule,
It is blocked through methyl acrylate, forms the hyperbranched modifying agent of amide esters, it, can well and coiled material containing a large amount of benzene radicals
In pitch it is compatible, while being formed by dissaving polymer and have an a large amount of cavity, space net structure is presented, with small molecule
Form exists, and along with the structure of elastomer macromolecular, works in coordination, asphaltene molecule can be made to be fixed on three-dimensional structure
In, so that the ability of anti-foreign matter insertion is enhanced, so that waterproof resistance is improved;
(3) magnesium nitrate is added in the present invention, urea is added in aluminum nitrate, and reaction generates magnalium hydrotalcite intercalated material, makes surface road
Lewis acid bit number of points, the infiltration of one side resisting chloride ion penetration reduce corrosion, and the inorganic laminate of another aspect multilayered structure is to ultraviolet
Line has strong physical reflection effect, can effectively reduce destruction of the high energy ultraviolet to material, to rise to ultraviolet light
To shield effectiveness, β-(4- hydroxy phenyl -3,5- di-t-butyl) propionic acid n-octadecyl alcohol ester, (2,4- bis- uncles of phosphorous acid three is added
Butyl phenyl) two kinds of antioxidant compoundings of ester, the inhibition and suspension of oxidation reaction are carried out, synergistic effect is formed, to waterproof roll
Ageing-resistant performance plays preferable protective effect.
Specific embodiment
Elastomer additives:
(1) it takes polytetramethylene ether glycol 2 ~ 5:1 in mass ratio ~ 4 that polycaprolactone is added, is warming up to 80 ~ 85 DEG C and is stirred
30 ~ 40min obtains mixture, takes mixture 10 ~ 20:1 in mass ratio ~ 3 that dimethylbenzene is added, and mixes 20 ~ 40min, it is cooled to 50 ~
60 DEG C, 2 ~ 4 times of polytetramethylene ether glycol quality of toluene di-isocyanate(TDI) is added, be warming up to 75 ~ 80 DEG C be stirred 1 ~
3h must stir mixture a;
(2) it takes three (2- ethoxy) isocyanuric acid ester 2 ~ 5:2 in mass ratio ~ 6 that triisopropanolamine is added, is warming up to 85 ~ 90 DEG C and stirs
20 ~ 30min of mixing is mixed, mixture a is obtained, takes stirring mixture a 10 ~ 15:2 in mass ratio ~ 5 that mixture a is added, adds stirring
The dibutyl tin dilaurate of mixture a mass 1 ~ 5% is stirred 1 ~ 3h in 80 ~ 85 DEG C, is cooled to room temperature to get elastomer
Additive.
Modifying agent:
S1. take trimellitic anhydride 1 ~ 3:10 in mass ratio ~ 20 that n,N-dimethylacetamide is added, it is stirred 1 in 45 ~ 55 DEG C ~
3h obtains mixed liquor a, take diisopropanol 2 ~ 4:10 in mass ratio ~ 15 be added n,N-dimethylacetamide, magnetic agitation 30 ~
50min obtains mixed liquor b, and 3 ~ 6:1 ~ 3 in mass ratio mixed liquor a is taken to be added dropwise in mixed liquor b, controls 30 ~ 50min of time for adding,
It is passed through nitrogen protection, 2 ~ 4h is stirred in 25 ~ 30 DEG C, obtains stirring mixture;
S2. take stirring mixture 80 ~ 90:6 in mass ratio ~ 9 that triethanolamine is added, addition is stirred amount of substance 0.5 ~ 1.5%
P-methyl benzenesulfonic acid is passed through nitrogen protection, adds the toluene for being stirred amount of substance 30 ~ 50%, is warming up to 130 ~ 135 DEG C of stirrings
Mix 3 ~ 5h, be cooled to room temperature, be evaporated under reduced pressure, obtain vacuum distillation object, take vacuum distillation object 20 ~ 30:1 in mass ratio ~ 4:0.1 ~
0.3 is added methyl acrylate, hydroquinone, adds the p-methyl benzenesulfonic acid of vacuum distillation amount of substance 1 ~ 4%, is warming up to 90 ~ 95 DEG C
It is stirred 10 ~ 12h, is evaporated under reduced pressure to get modifying agent.
Uvioresistant absorbing additives: take magnesium nitrate 3 ~ 6:1 in mass ratio ~ 3:15 ~ 20 that aluminum nitrate, absolute ethyl alcohol and stirring is added
30 ~ 40min is mixed, the urea of dehydrated alcohol quality 50 ~ 60% is added, 20 ~ 30min of ultrasonic disperse is stirred in 140 ~ 150 DEG C
Mixing 18 ~ for 24 hours, it is cooled to room temperature, is centrifuged, precipitating is taken to wash through deionized water, it is dry, it grinds and sieves with 100 mesh sieve, collected
Particle is sieved to get uvioresistant absorbing additives.
Antioxidant: (4- hydroxy phenyl -3,5- di-t-butyl) propionic acid n-octadecyl alcohol ester 1 ~ 4:3 ~ 6 in mass ratio β-are taken to add
Enter (2, the 4- di-tert-butyl-phenyl) ester of phosphorous acid three mixing to get.
A kind of preparation method of waterproof roll, includes the following steps:
A. according to the mass fraction, take 100# asphalt heating to be stirred 30 ~ 50min to 170 ~ 180 DEG C, 100# asphalt quality is added
20 ~ 50% 10# pitch, is stirred 20 ~ 30min, the elastomer additives of 100# asphalt quality 20 ~ 40% is added, in 100
~ 120 DEG C are stirred 1 ~ 3h, obtain matrix object;
B. as mass fraction, 8 ~ 12 parts of modifying agent, 5 ~ 8 parts of uvioresistant absorbing additives, 1 ~ 4 part of antioxidant, 20 ~ 30 parts of cunnings are taken
Mountain flour is stirred 1 ~ 3h in 75 ~ 80 DEG C, obtains mixture b, takes mixture b 3 ~ 5:10 in mass ratio ~ 30 that matrix object is added mixed
It closes, is stirred 40 ~ 50min in 170 ~ 180 DEG C, obtains maceration extract, polyester felt is taken to immerse maceration extract, keep 3 ~ 5min, take out leaching
Polyester felt tabletting after stain, it is dry to get anti-coiled material.
Elastomer additives
(1) it takes polytetramethylene ether glycol 2:1 in mass ratio that polycaprolactone is added, is warming up to 80 DEG C and is stirred 30min, obtain
Mixture takes mixture 10:1 in mass ratio that dimethylbenzene is added, and mixes 20min, is cooled to 50 DEG C, and polytetramethylene ether second is added
The toluene di-isocyanate(TDI) that 2 times of glycol quality is warming up to 75 DEG C and is stirred 1h, must stir mixture a;
(2) it takes three (2- ethoxy) isocyanuric acid ester 2:2 in mass ratio that triisopropanolamine is added, is warming up to 85 DEG C and is stirred
20min obtains mixture a, takes stirring mixture a 10:2 in mass ratio that mixture a is added, and adds stirring mixture a mass 1%
Dibutyl tin dilaurate, be stirred 1h in 80 DEG C, be cooled to room temperature to get elastomer additives.
Modifying agent:
S1. it takes trimellitic anhydride 1:10 in mass ratio that n,N-dimethylacetamide is added, is stirred 1h in 45 DEG C, must mix
Liquid a, takes diisopropanol 2:10 in mass ratio that n,N-dimethylacetamide is added, and magnetic agitation 30min obtains mixed liquor b, takes mixing
Liquid a 3:1 in mass ratio is added dropwise in mixed liquor b, is controlled time for adding 30min, is passed through nitrogen protection, is stirred in 25 DEG C
2h obtains stirring mixture;
S2. take stirring mixture 80:6 in mass ratio be added triethanolamine, be added be stirred amount of substance 0.5% to toluene sulphur
Acid is passed through nitrogen protection, adds the toluene for being stirred amount of substance 30%, is warming up to 130 DEG C and is stirred 3h, is cooled to room
Temperature, vacuum distillation, obtains vacuum distillation object, takes vacuum distillation object 20:1:0.1 in mass ratio that methyl acrylate, hydroquinone is added,
The p-methyl benzenesulfonic acid for adding vacuum distillation amount of substance 1% is warming up to 90 DEG C and is stirred 10h, is evaporated under reduced pressure to get modifying agent.
Uvioresistant absorbing additives: take magnesium nitrate 3:1:15 in mass ratio that aluminum nitrate, absolute ethyl alcohol and stirring mixing is added
30min, adds the urea of dehydrated alcohol quality 50%, and ultrasonic disperse 20min is stirred 18h in 140 DEG C, is cooled to room
Temperature, centrifugation take precipitating to wash through deionized water, dry, grind and sieve with 100 mesh sieve, and collect sieving particle to get uvioresistant suction
Receive additive.
Antioxidant: β-(4- hydroxy phenyl -3,5- di-t-butyl) propionic acid n-octadecyl alcohol ester 1:3 in mass ratio is taken to be added sub-
Tricresyl phosphate (2,4- di-tert-butyl-phenyl) ester mixing to get.
A kind of preparation method of waterproof roll, includes the following steps:
A. according to the mass fraction, take 100# asphalt heating to be stirred 30min to 170 DEG C, 100# asphalt quality 20% is added
10# pitch, is stirred 20min, adds the elastomer additives of 100# asphalt quality 20%, is stirred 1h in 100 DEG C,
Obtain matrix object;
B. as mass fraction, 8 parts of modifying agent, 5 parts of uvioresistant absorbing additives, 1 part of antioxidant, 20 parts of talcum powder are taken, in 75
DEG C it is stirred 1h, obtains mixture b, taken mixture b 3:10 in mass ratio that the mixing of matrix object is added, be stirred in 170 DEG C
40min obtains maceration extract, and polyester felt is taken to immerse maceration extract, keeps 3min, takes out polyester felt tabletting after dipping, dry to get anti-roll
Material.
Elastomer additives:
(1) it takes polytetramethylene ether glycol 4:3 in mass ratio that polycaprolactone is added, is warming up to 83 DEG C and is stirred 35min, obtain
Mixture takes mixture 15:2 in mass ratio that dimethylbenzene is added, and mixes 30min, is cooled to 55 DEG C, and polytetramethylene ether second is added
The toluene di-isocyanate(TDI) that 3 times of glycol quality is warming up to 78 DEG C and is stirred 2h, must stir mixture a;
(2) it takes three (2- ethoxy) isocyanuric acid ester 3:4 in mass ratio that triisopropanolamine is added, is warming up to 88 DEG C and is stirred
25min obtains mixture a, takes stirring mixture a 13:4 in mass ratio that mixture a is added, and adds stirring mixture a mass 3%
Dibutyl tin dilaurate, be stirred 2h in 83 DEG C, be cooled to room temperature to get elastomer additives.
Modifying agent:
S1. it takes trimellitic anhydride 2:15 in mass ratio that n,N-dimethylacetamide is added, is stirred 2h in 50 DEG C, must mix
Liquid a, takes diisopropanol 3:13 in mass ratio that n,N-dimethylacetamide is added, and magnetic agitation 35min obtains mixed liquor b, takes mixing
Liquid a 4:2 in mass ratio is added dropwise in mixed liquor b, is controlled time for adding 40min, is passed through nitrogen protection, is stirred in 28 DEG C
3h obtains stirring mixture;
S2. it takes stirring mixture 85:7 in mass ratio that triethanolamine is added, the p-methyl benzenesulfonic acid for being stirred amount of substance 1% is added,
It is passed through nitrogen protection, adds the toluene for being stirred amount of substance 40%, 132 DEG C is warming up to and is stirred 4h, be cooled to room temperature,
Vacuum distillation, obtains vacuum distillation object, takes vacuum distillation object 25:3:0.2 in mass ratio that methyl acrylate, hydroquinone is added, then
The p-methyl benzenesulfonic acid of vacuum distillation amount of substance 1 ~ 4% is added, is warming up to 93 DEG C and is stirred 11h, be evaporated under reduced pressure to get modifying agent.
Uvioresistant absorbing additives: take magnesium nitrate 5:2:18 in mass ratio that aluminum nitrate, absolute ethyl alcohol and stirring mixing is added
35min, adds the urea of dehydrated alcohol quality 55%, and ultrasonic disperse 25min is stirred 22h in 145 DEG C, is cooled to room
Temperature, centrifugation take precipitating to wash through deionized water, dry, grind and sieve with 100 mesh sieve, and collect sieving particle to get uvioresistant suction
Receive additive.
Antioxidant: β-(4- hydroxy phenyl -3,5- di-t-butyl) propionic acid n-octadecyl alcohol ester 3:5 in mass ratio is taken to be added sub-
Tricresyl phosphate (2,4- di-tert-butyl-phenyl) ester mixing to get.
A kind of preparation method of waterproof roll, includes the following steps:
A. according to the mass fraction, take 100# asphalt heating to be stirred 40min to 175 DEG C, 100# asphalt quality 40% is added
10# pitch, is stirred 25min, adds the elastomer additives of 100# asphalt quality 30%, is stirred 2h in 110 DEG C,
Obtain matrix object;
B. as mass fraction, 10 parts of modifying agent, 6 parts of uvioresistant absorbing additives, 3 parts of antioxidant, 25 parts of talcum powder are taken, in 78
DEG C it is stirred 2h, obtains mixture b, taken mixture b 4:20 in mass ratio that the mixing of matrix object is added, be stirred in 175 DEG C
45min obtains maceration extract, and polyester felt is taken to immerse maceration extract, keeps 4min, takes out polyester felt tabletting after dipping, dry to get anti-roll
Material.
Elastomer additives:
(1) it takes polytetramethylene ether glycol 5:4 in mass ratio that polycaprolactone is added, is warming up to 85 DEG C and is stirred 40min, obtain
Mixture takes mixture 20:3 in mass ratio that dimethylbenzene is added, and mixes 40min, is cooled to 60 DEG C, and polytetramethylene ether second is added
The toluene di-isocyanate(TDI) that 4 times of glycol quality is warming up to 80 DEG C and is stirred 3h, must stir mixture a;
(2) it takes three (2- ethoxy) isocyanuric acid ester 5:6 in mass ratio that triisopropanolamine is added, is warming up to 90 DEG C and is stirred
30min obtains mixture a, takes stirring mixture a 15:5 in mass ratio that mixture a is added, and adds stirring mixture a mass 5%
Dibutyl tin dilaurate, be stirred 3h in 85 DEG C, be cooled to room temperature to get elastomer additives.
Modifying agent:
S1. it takes trimellitic anhydride 3:20 in mass ratio that n,N-dimethylacetamide is added, is stirred 3h in 55 DEG C, must mix
Liquid a, takes diisopropanol 4:15 in mass ratio that n,N-dimethylacetamide is added, and magnetic agitation 50min obtains mixed liquor b, takes mixing
Liquid a 6:3 in mass ratio is added dropwise in mixed liquor b, is controlled time for adding 50min, is passed through nitrogen protection, is stirred in 30 DEG C
4h obtains stirring mixture;
S2. take stirring mixture 90:9 in mass ratio be added triethanolamine, be added be stirred amount of substance 1.5% to toluene sulphur
Acid is passed through nitrogen protection, adds the toluene for being stirred amount of substance 50%, is warming up to 135 DEG C and is stirred 5h, is cooled to room
Temperature, vacuum distillation, obtains vacuum distillation object, takes vacuum distillation object 30:4:0.3 in mass ratio that methyl acrylate, hydroquinone is added,
The p-methyl benzenesulfonic acid for adding vacuum distillation amount of substance 4% is warming up to 95 DEG C and is stirred 12h, is evaporated under reduced pressure to get modifying agent.
Uvioresistant absorbing additives: take magnesium nitrate 6:3:20 in mass ratio that aluminum nitrate, absolute ethyl alcohol and stirring mixing is added
40min, adds the urea of dehydrated alcohol quality 60%, and ultrasonic disperse 30min is stirred for 24 hours in 150 DEG C, is cooled to room
Temperature, centrifugation take precipitating to wash through deionized water, dry, grind and sieve with 100 mesh sieve, and collect sieving particle to get uvioresistant suction
Receive additive.
Antioxidant: β-(4- hydroxy phenyl -3,5- di-t-butyl) propionic acid n-octadecyl alcohol ester 4:6 in mass ratio is taken to be added sub-
Tricresyl phosphate (2,4- di-tert-butyl-phenyl) ester mixing to get.
A kind of preparation method of waterproof roll, includes the following steps:
A. according to the mass fraction, take 100# asphalt heating to be stirred 50min to 180 DEG C, 100# asphalt quality 50% is added
10# pitch, is stirred 30min, adds the elastomer additives of 100# asphalt quality 40%, is stirred 3h in 120 DEG C,
Obtain matrix object;
B. as mass fraction, 12 parts of modifying agent, 8 parts of uvioresistant absorbing additives, 4 parts of antioxidant, 30 parts of talcum powder are taken, in 80
DEG C it is stirred 3h, obtains mixture b, taken mixture b 5:30 in mass ratio that the mixing of matrix object is added, be stirred in 180 DEG C
50min obtains maceration extract, and polyester felt is taken to immerse maceration extract, keeps 5min, takes out polyester felt tabletting after dipping, dry to get waterproof
Coiled material.
Comparative example 1: it is essentially identical with the preparation method of embodiment 1, it has only the difference is that lacking elastomer additives.
Comparative example 2: it is essentially identical with the preparation method of embodiment 1, it has only the difference is that lacking modifying agent.
Comparative example 3: it is essentially identical with the preparation method of embodiment 1, it has only the difference is that lacking uvioresistant absorbing additives.
Comparative example 4: it is essentially identical with the preparation method of embodiment 1, it has only the difference is that lacking antioxidant.
Comparative example 5: the waterproof roll of company of Nantong City production.
By embodiment waterproof roll and comparative example obtained by waterproof roll survey according to GB/23457-2009 standard
Examination, test result are as shown in table 1:
Table 1:
In summary, waterproof roll of the invention is more preferable compared to commercial product effect, is worth promoting.
Claims (7)
1. a kind of waterproof roll, which is characterized in that including elastomer additives, modifying agent, uvioresistant absorbing additives, antioxygen
Agent;
The preparation method of the elastomer additives, includes the following steps:
(1) it takes polytetramethylene ether glycol 2 ~ 5:1 in mass ratio ~ 4 that polycaprolactone is added, is warming up to 80 ~ 85 DEG C and is stirred,
Mixture is obtained, takes mixture 10 ~ 20:1 in mass ratio ~ 3 that dimethylbenzene mixing is added, is cooled to 50 ~ 60 DEG C, polytetramethylene is added
The toluene di-isocyanate(TDI) that 2 ~ 4 times of ether quality of glycol is stirred, and must stir mixture a;
(2) it takes three (2- ethoxy) isocyanuric acid ester 2 ~ 5:2 in mass ratio ~ 6 that triisopropanolamine is added, is warming up to 85 ~ 90 DEG C and stirs
Mixing is mixed, mixture a is obtained, takes stirring mixture a 10 ~ 15:2 in mass ratio ~ 5 that mixture a is added, adds stirring mixture a
The dibutyl tin dilaurate of quality 1 ~ 5% is stirred in 80 ~ 85 DEG C, is cooled to room temperature to get elastomer additives.
2. waterproof roll according to claim 1, which is characterized in that the stirring of stirring mixture a is mixed in the step (1)
Conjunction condition are as follows: be warming up to 75 ~ 80 DEG C and be stirred 1 ~ 3h.
3. waterproof roll according to claim 1, which is characterized in that the preparation method of the modifying agent, including walk as follows
It is rapid:
S1. it takes trimellitic anhydride 1 ~ 3:10 in mass ratio ~ 20 that n,N-dimethylacetamide is added, is stirred in 45 ~ 55 DEG C,
Mixed liquor a is obtained, takes diisopropanol 2 ~ 4:10 in mass ratio ~ 15 that n,N-dimethylacetamide is added, 30 ~ 50min of magnetic agitation is obtained
Mixed liquor b takes 3 ~ 6:3 ~ 5 in mass ratio mixed liquor a to be added dropwise in mixed liquor b, controls 30 ~ 50min of time for adding, is passed through nitrogen
Protection, is stirred in 25 ~ 30 DEG C, obtains stirring mixture;
S2. take stirring mixture 80 ~ 90:6 in mass ratio ~ 9 that triethanolamine is added, addition is stirred amount of substance 0.5 ~ 1.5%
P-methyl benzenesulfonic acid is passed through nitrogen protection, adds the toluene for being stirred amount of substance 30 ~ 50%, is warming up to 130 ~ 135 DEG C of stirrings
Mixing, is cooled to room temperature, and is evaporated under reduced pressure, obtains vacuum distillation object, and vacuum distillation object 20 ~ 30:1 in mass ratio ~ 4:0.1 ~ 0.3 is taken to add
Enter methyl acrylate, hydroquinone, adds the p-methyl benzenesulfonic acid of vacuum distillation amount of substance 1 ~ 4%, be warming up to 90 ~ 95 DEG C of stirrings
10 ~ 12h is mixed, is evaporated under reduced pressure to get modifying agent.
4. waterproof roll according to claim 1, which is characterized in that the preparation method of the uvioresistant absorbing additives,
Include the following steps:
It takes magnesium nitrate 3 ~ 6:1 in mass ratio ~ 3:15 ~ 20 that aluminum nitrate, absolute ethyl alcohol and stirring mixing is added, adds dehydrated alcohol matter
The urea of amount 50 ~ 60%, ultrasonic disperse are stirred in 140 ~ 150 DEG C, are cooled to room temperature, and are centrifuged, and take precipitating through deionized water
Washing, it is dry, it grinds and sieves with 100 mesh sieve, collect sieving particle to get uvioresistant absorbing additives.
5. waterproof roll according to claim 1, which is characterized in that the antioxidant are as follows: take β-(hydroxy phenyl -3 4-,
5- di-t-butyl) that (2,4- di-tert-butyl-phenyl) ester of phosphorous acid three is added is mixed by propionic acid n-octadecyl alcohol ester 1 ~ 4:3 in mass ratio ~ 6
Close to get.
6. a kind of preparation method of the waterproof roll as described in claim 1 ~ 5 any one, which is characterized in that the preparation method
Include the following steps:
A. according to the mass fraction, take 100# asphalt heating to be stirred to 170 ~ 180 DEG C, 100# asphalt quality 20 ~ 50% is added
The mixing of 10# asphalt mixing, adds the elastomer additives of 100# asphalt quality 20 ~ 40%, is stirred, obtains in 100 ~ 120 DEG C
Matrix object;
B. as mass fraction, 8 ~ 12 parts of modifying agent, 5 ~ 8 parts of uvioresistant absorbing additives, 1 ~ 4 part of antioxidant, 20 ~ 30 parts of cunnings are taken
Mountain flour is stirred in 75 ~ 80 DEG C, obtains mixture b, takes mixture b 3 ~ 5:10 in mass ratio ~ 30 that the stirring of matrix object is added mixed
It closes, obtains maceration extract, polyester felt is taken to immerse maceration extract, keep 3 ~ 5min, take out polyester felt tabletting after dipping, it is dry to get anti-roll
Material.
7. the preparation method of waterproof roll according to claim 6, which is characterized in that maceration extract stirs in the step B
Mix mixing condition are as follows: be stirred 40 ~ 50min in 170 ~ 180 DEG C.
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114672264A (en) * | 2022-04-06 | 2022-06-28 | 安徽省奥佳建材有限公司 | Elastic self-adhesive waterproof roll and preparation method thereof |
EP4127009A4 (en) * | 2020-03-30 | 2024-01-10 | Dow Global Technologies Llc | Polyurethane compositions, products prepared with same and preparation methods thereof |
Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS55164147A (en) * | 1979-06-09 | 1980-12-20 | Yoshi Takiguchi | Heat insulating waterproof material |
EP0483995A1 (en) * | 1990-10-24 | 1992-05-06 | Fibrescreed Limited | Waterproofing material |
CN101580572A (en) * | 2008-05-14 | 2009-11-18 | 聚益化学工业股份有限公司 | Aqueous moisture-permeability waterproof resin composition |
CN102115524A (en) * | 2009-12-30 | 2011-07-06 | 上海合达聚合物科技有限公司 | Fluorine-containing polyurethane and preparation method thereof |
CN102585144A (en) * | 2011-12-23 | 2012-07-18 | 烟台万华聚氨酯股份有限公司 | Reaction type polyurethane modified asphalt waterproof coiled material and preparation method thereof |
CN104263261A (en) * | 2014-10-10 | 2015-01-07 | 南安市国高建材科技有限公司 | High initial adhesion self-adhering waterproof roll and preparation method |
CN105238084A (en) * | 2015-09-24 | 2016-01-13 | 天长市金牛防水防腐材料有限公司 | Heat-resistance and saline-alkaline-resistance type elastomer modified bitumen waterproof coil material |
CN105440259A (en) * | 2015-12-16 | 2016-03-30 | 陕西科技大学 | Hyperbranched waterborne polyurethane with isocyanurate as core and preparation method thereof |
CN105949470A (en) * | 2016-03-03 | 2016-09-21 | 济南大学 | Application of hyper-branched polymer in improvement on cohesiveness of modified asphalt in water permeable asphalt pavement |
CN106928422A (en) * | 2017-04-28 | 2017-07-07 | 广东工业大学 | A kind of resisting high-temperature yellowing polyurethane and preparation method thereof |
CN107384293A (en) * | 2017-06-28 | 2017-11-24 | 苏州奥斯汀新材料科技有限公司 | A kind of preparation method of thermoplastic polyurethane hot melt adhesive |
CN107406569A (en) * | 2015-03-04 | 2017-11-28 | Sika技术股份公司 | Improved low temperature impact performance in polyurethane impact modifier based on PTMEG |
CN108099306A (en) * | 2017-11-21 | 2018-06-01 | 广西武宣金牌防水材料科技有限公司 | A kind of polyurethane-modified asphalt water-proof coiled material and its production method |
CN108250999A (en) * | 2018-01-30 | 2018-07-06 | 富华防水科技股份有限公司 | A kind of non-bituminous base self-adhesion polymer membranes and preparation method thereof |
-
2018
- 2018-08-17 CN CN201810943356.7A patent/CN109097998A/en active Pending
Patent Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS55164147A (en) * | 1979-06-09 | 1980-12-20 | Yoshi Takiguchi | Heat insulating waterproof material |
EP0483995A1 (en) * | 1990-10-24 | 1992-05-06 | Fibrescreed Limited | Waterproofing material |
CN101580572A (en) * | 2008-05-14 | 2009-11-18 | 聚益化学工业股份有限公司 | Aqueous moisture-permeability waterproof resin composition |
CN102115524A (en) * | 2009-12-30 | 2011-07-06 | 上海合达聚合物科技有限公司 | Fluorine-containing polyurethane and preparation method thereof |
CN102585144A (en) * | 2011-12-23 | 2012-07-18 | 烟台万华聚氨酯股份有限公司 | Reaction type polyurethane modified asphalt waterproof coiled material and preparation method thereof |
CN104263261A (en) * | 2014-10-10 | 2015-01-07 | 南安市国高建材科技有限公司 | High initial adhesion self-adhering waterproof roll and preparation method |
CN107406569A (en) * | 2015-03-04 | 2017-11-28 | Sika技术股份公司 | Improved low temperature impact performance in polyurethane impact modifier based on PTMEG |
CN105238084A (en) * | 2015-09-24 | 2016-01-13 | 天长市金牛防水防腐材料有限公司 | Heat-resistance and saline-alkaline-resistance type elastomer modified bitumen waterproof coil material |
CN105440259A (en) * | 2015-12-16 | 2016-03-30 | 陕西科技大学 | Hyperbranched waterborne polyurethane with isocyanurate as core and preparation method thereof |
CN105949470A (en) * | 2016-03-03 | 2016-09-21 | 济南大学 | Application of hyper-branched polymer in improvement on cohesiveness of modified asphalt in water permeable asphalt pavement |
CN106928422A (en) * | 2017-04-28 | 2017-07-07 | 广东工业大学 | A kind of resisting high-temperature yellowing polyurethane and preparation method thereof |
CN107384293A (en) * | 2017-06-28 | 2017-11-24 | 苏州奥斯汀新材料科技有限公司 | A kind of preparation method of thermoplastic polyurethane hot melt adhesive |
CN108099306A (en) * | 2017-11-21 | 2018-06-01 | 广西武宣金牌防水材料科技有限公司 | A kind of polyurethane-modified asphalt water-proof coiled material and its production method |
CN108250999A (en) * | 2018-01-30 | 2018-07-06 | 富华防水科技股份有限公司 | A kind of non-bituminous base self-adhesion polymer membranes and preparation method thereof |
Non-Patent Citations (1)
Title |
---|
蒋传磊: "一种超支化聚合物对煤沥青的改性及其在防水卷材中的应用", 《济南大学硕士学位论文》 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP4127009A4 (en) * | 2020-03-30 | 2024-01-10 | Dow Global Technologies Llc | Polyurethane compositions, products prepared with same and preparation methods thereof |
CN114672264A (en) * | 2022-04-06 | 2022-06-28 | 安徽省奥佳建材有限公司 | Elastic self-adhesive waterproof roll and preparation method thereof |
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