CN113248938A - Wet-cured polyurethane modified cold-mix asphalt and preparation method thereof - Google Patents
Wet-cured polyurethane modified cold-mix asphalt and preparation method thereof Download PDFInfo
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- CN113248938A CN113248938A CN202110683848.9A CN202110683848A CN113248938A CN 113248938 A CN113248938 A CN 113248938A CN 202110683848 A CN202110683848 A CN 202110683848A CN 113248938 A CN113248938 A CN 113248938A
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- asphalt
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- 239000010426 asphalt Substances 0.000 title claims abstract description 93
- 229920002635 polyurethane Polymers 0.000 title claims abstract description 45
- 239000004814 polyurethane Substances 0.000 title claims abstract description 45
- 238000002360 preparation method Methods 0.000 title abstract description 10
- 239000000203 mixture Substances 0.000 claims abstract description 53
- 229920001730 Moisture cure polyurethane Polymers 0.000 claims abstract description 23
- 239000011159 matrix material Substances 0.000 claims abstract description 20
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 17
- 238000001723 curing Methods 0.000 claims abstract description 17
- 238000013008 moisture curing Methods 0.000 claims abstract description 16
- 239000002904 solvent Substances 0.000 claims abstract description 15
- 239000002274 desiccant Substances 0.000 claims abstract description 12
- 239000003381 stabilizer Substances 0.000 claims abstract description 12
- 239000004721 Polyphenylene oxide Substances 0.000 claims abstract description 9
- 125000005442 diisocyanate group Chemical group 0.000 claims abstract description 9
- 229920000570 polyether Polymers 0.000 claims abstract description 9
- 150000004658 ketimines Chemical group 0.000 claims abstract description 8
- 239000004014 plasticizer Substances 0.000 claims abstract description 7
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 5
- 150000002009 diols Chemical class 0.000 claims abstract description 5
- 229920000642 polymer Polymers 0.000 claims abstract description 3
- 239000002994 raw material Substances 0.000 claims abstract description 3
- 238000010008 shearing Methods 0.000 claims description 23
- 238000002156 mixing Methods 0.000 claims description 17
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 14
- 238000010438 heat treatment Methods 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 12
- 238000003756 stirring Methods 0.000 claims description 12
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 10
- -1 polyethylene Polymers 0.000 claims description 9
- 238000001816 cooling Methods 0.000 claims description 7
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 6
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 claims description 6
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 6
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 claims description 5
- 239000005057 Hexamethylene diisocyanate Substances 0.000 claims description 5
- 239000000292 calcium oxide Substances 0.000 claims description 5
- 235000012255 calcium oxide Nutrition 0.000 claims description 5
- 229920001971 elastomer Polymers 0.000 claims description 5
- 229920005989 resin Polymers 0.000 claims description 5
- 239000011347 resin Substances 0.000 claims description 5
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims description 5
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims description 4
- 238000007789 sealing Methods 0.000 claims description 4
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims description 3
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 claims description 3
- 239000004698 Polyethylene Substances 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 claims description 3
- 239000001110 calcium chloride Substances 0.000 claims description 3
- 229910001628 calcium chloride Inorganic materials 0.000 claims description 3
- 239000001913 cellulose Substances 0.000 claims description 3
- 229920002678 cellulose Polymers 0.000 claims description 3
- 239000002283 diesel fuel Substances 0.000 claims description 3
- UTZKJCIQQWLQPV-UHFFFAOYSA-N ethane-1,2-diol;propane-1,2-diol Chemical compound OCCO.OCCO.CC(O)CO UTZKJCIQQWLQPV-UHFFFAOYSA-N 0.000 claims description 3
- 229910052943 magnesium sulfate Inorganic materials 0.000 claims description 3
- 235000019341 magnesium sulphate Nutrition 0.000 claims description 3
- 229920000573 polyethylene Polymers 0.000 claims description 3
- 229920001451 polypropylene glycol Polymers 0.000 claims description 3
- 229920000909 polytetrahydrofuran Polymers 0.000 claims description 3
- 229920000428 triblock copolymer Polymers 0.000 claims description 3
- 239000001993 wax Substances 0.000 claims description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 2
- KXBFLNPZHXDQLV-UHFFFAOYSA-N [cyclohexyl(diisocyanato)methyl]cyclohexane Chemical compound C1CCCCC1C(N=C=O)(N=C=O)C1CCCCC1 KXBFLNPZHXDQLV-UHFFFAOYSA-N 0.000 claims description 2
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 claims description 2
- 235000011148 calcium chloride Nutrition 0.000 claims description 2
- 235000011132 calcium sulphate Nutrition 0.000 claims description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 239000003350 kerosene Substances 0.000 claims description 2
- 229920005610 lignin Polymers 0.000 claims description 2
- 239000012188 paraffin wax Substances 0.000 claims description 2
- 230000035515 penetration Effects 0.000 claims description 2
- 239000003208 petroleum Substances 0.000 claims description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 2
- 230000000052 comparative effect Effects 0.000 description 7
- 150000001412 amines Chemical class 0.000 description 5
- 238000010276 construction Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 4
- 239000004970 Chain extender Substances 0.000 description 3
- SYBYTAAJFKOIEJ-UHFFFAOYSA-N 3-Methylbutan-2-one Chemical compound CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000004134 energy conservation Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 229940018564 m-phenylenediamine Drugs 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- KRIOVPPHQSLHCZ-UHFFFAOYSA-N phenyl propionaldehyde Natural products CCC(=O)C1=CC=CC=C1 KRIOVPPHQSLHCZ-UHFFFAOYSA-N 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920000468 styrene butadiene styrene block copolymer Polymers 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L95/00—Compositions of bituminous materials, e.g. asphalt, tar, pitch
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3225—Polyamines
- C08G18/3253—Polyamines being in latent form
- C08G18/3256—Reaction products of polyamines with aldehydes or ketones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4833—Polyethers containing oxyethylene units
- C08G18/4837—Polyethers containing oxyethylene units and other oxyalkylene units
- C08G18/4841—Polyethers containing oxyethylene units and other oxyalkylene units containing oxyethylene end groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4854—Polyethers containing oxyalkylene groups having four carbon atoms in the alkylene group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5021—Polyethers having heteroatoms other than oxygen having nitrogen
- C08G18/5024—Polyethers having heteroatoms other than oxygen having nitrogen containing primary and/or secondary amino groups
- C08G18/503—Polyethers having heteroatoms other than oxygen having nitrogen containing primary and/or secondary amino groups being in latent form
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/60—Polyamides or polyester-amides
- C08G18/603—Polyamides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/16—Halogen-containing compounds
- C08K2003/162—Calcium, strontium or barium halides, e.g. calcium, strontium or barium chloride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2206—Oxides; Hydroxides of metals of calcium, strontium or barium
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/30—Sulfur-, selenium- or tellurium-containing compounds
- C08K2003/3045—Sulfates
- C08K2003/3063—Magnesium sulfate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2555/00—Characteristics of bituminous mixtures
- C08L2555/20—Mixtures of bitumen and aggregate defined by their production temperatures, e.g. production of asphalt for road or pavement applications
- C08L2555/28—Asphalt produced between 0°C and below 65°C, e.g. cold mix asphalt produced between 0°C and 35°C
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Civil Engineering (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
The invention provides a wet cured polyurethane modified cold mix asphalt and a preparation method thereof, wherein the wet cured polyurethane modified cold mix asphalt comprises the following raw materials in parts by weight: 60-75 parts of matrix asphalt, 10-20 parts of solvent, 5-15 parts of polyurethane prepolymer, 2-5 parts of plasticizer, 1-4 parts of drying agent, 1-3 parts of stabilizer and 0.5-1.5 parts of moisture curing agent. The polyurethane prepolymer is an isocyanate-terminated base-line polymer prepared from polyether diol and diisocyanate, and the moisture curing agent is a ketimine curing agent. The cold-mix asphalt mixture prepared by the invention can be mixed and paved at normal temperature/low temperature, moisture induces the polyurethane prepolymer to be crosslinked and cured after paving, the formation of the cold-mix asphalt pavement strength is accelerated, the Marshall stability is 7.7-8.6KN, the residual stability is more than 90%, and the requirement of quick traffic of cold-mix asphalt roads is met.
Description
Technical Field
The invention relates to the technical field of road materials, in particular to damp-cured polyurethane modified cold-mix asphalt and a preparation method thereof.
Background
The cold-mix asphalt mixture has the advantages of energy conservation, environmental protection, storage, convenient construction and the like, but has common key engineering problems of low initial stability, poor anti-rutting performance and the like. At present, the road performance of the cold-mixed asphalt mixture can be improved to a certain extent by modifying the cold-mixed asphalt by using high polymer materials such as epoxy resin, polyurethane, SBR, SBS and the like, but the essence of low stability and long curing time is not changed, the requirement of timely vehicle traffic after paving cannot be met, and the development and large-scale engineering application of the cold-mixed asphalt mixture are limited.
Different from the storable cold-mix asphalt mixture, the patent CN106977966A proposes a cold-mix cold-spread epoxy modified asphalt material and a preparation method thereof, and the patent CN111718154A proposes a preparation method of an epoxy modified cold-patch asphalt mixture. The two methods firstly prepare the component A and the component B respectively, and when the two components are used, the two components are mixed, reacted and solidified again so as to meet the requirements of paving on the same day and opening traffic on the same day. However, the two methods are complex in process, and A, B components are mixed to generate a curing reaction, so that the curing reaction cannot be stored, the curing reaction needs to be prepared at present, and the curing reaction is mostly suitable for repairing pits and diseases of pavements and small-scale application of municipal roads.
Disclosure of Invention
The invention provides a damp-cured polyurethane modified cold-mix asphalt and a preparation method thereof, which solve the problems of low stability, long curing time or complex process and incapability of storage of the existing cold-mix asphalt.
The technical scheme for realizing the invention is as follows:
the damp-cured polyurethane modified cold-mix asphalt comprises the following raw materials in parts by weight: 60-75 parts of matrix asphalt, 10-20 parts of solvent, 5-15 parts of polyurethane prepolymer, 2-5 parts of plasticizer, 1-4 parts of drying agent, 1-3 parts of stabilizer and 0.5-1.5 parts of moisture curing agent.
The method comprises the following steps:
(1) adding the matrix asphalt into a shearing and stirring kettle, heating to 90-120 ℃ to completely melt the matrix asphalt, sequentially adding a solvent, a plasticizer, a polyurethane prepolymer and a drying agent, and shearing and mixing at the speed of 1000-2000r/min for 60-120min to obtain the polyurethane modified cold-mix asphalt.
(2) And cooling the polyurethane modified cold-mixed asphalt to 60-80 ℃, adding a stabilizer and a moisture curing agent, and shearing and mixing at the speed of 800-.
The matrix asphalt is 70# petroleum asphalt with penetration degree of 50-70mm (25 ℃), softening point of 45-55 ℃ and ductility of more than 100cm (15 ℃).
The solvent is one or a combination of more of kerosene, diesel oil, 180# solvent oil or 200# solvent oil.
The polyurethane prepolymer is an isocyanate-terminated base-line polymer synthesized by polyether diol and diisocyanate. Adding diisocyanate into a reaction kettle, heating to 70-90 ℃, keeping the diisocyanate slightly excessive, adding polyether glycol into the reaction kettle for 2-3 times, keeping the temperature at 70-90 ℃, and stirring for reaction for 60-120min to obtain the isocyanate-terminated base-line type polyurethane prepolymer.
The polyether diol is one or the combination of a plurality of polypropylene glycol, polytetrahydrofuran ether glycol, ethylene glycol-propylene glycol-ethylene glycol triblock copolymer and polyoxyethylene glycol, the hydroxyl value is 60-120mg KOH/g, and the molecular weight is 1200-2000.
The diisocyanate is one or a combination of Toluene Diisocyanate (TDI), Hexamethylene Diisocyanate (HDI), diphenylmethane diisocyanate (MDI) or dicyclohexylmethane diisocyanate (HMDI).
The plasticizer is one or a combination of several of polyethylene wax, chlorinated paraffin, sasobit resin, ethylene vinyl acetate or dioctyl phthalate.
The drying agent is one or the combination of several of calcium sulfate, magnesium sulfate, calcium chloride or quicklime.
The moist curing agent is ketimine. The ketimine is prepared by the reaction of one of methyl isopropyl ketone, acetophenone and methyl isobutyl ketone with one of low molecular polyamide, polyether amine, phenol aldehyde amine and m-phenylenediamine, and the reaction temperature is 140 ℃ and 170 ℃. The ketimine generates reverse reaction when meeting water, and regenerates amine chain extender, which can crosslink and cure linear polyurethane in humid air.
The stabilizer is one or a combination of several of sulfur powder, rubber oil, cellulose and lignin.
The moisture-curing polyurethane modified cold-mix asphalt needs vacuum sealing storage, and can also be prepared into a cold-mix asphalt mixture and then stored in a vacuum sealing manner, so that the contact with moisture air is avoided, and the moisture-curing polyurethane modified cold-mix asphalt is free from pre-curing.
The invention has the beneficial effects that:
(1) according to the invention, the isocyanate-terminated polyurethane prepolymer and the moisture curing agent are introduced into the cold-mixed asphalt, the moisture curing agent and moisture are subjected to reverse reaction after being paved to generate the amine chain extender, the polyurethane prepolymer is induced to be crosslinked and cured, the strength formation and the stability improvement of the cold-mixed asphalt pavement are accelerated, and the requirement of quick traffic is met.
(2) The cold-mix asphalt and the mixture thereof prepared by the invention can be stored in a vacuum-pumping and sealing way without being prepared at present. The product has good workability and convenient construction, is in contact reaction and solidification with moisture after being paved, accelerates the formation of the strength of the cold-mixed asphalt pavement, has the Marshall stability of 7.7-8.6KN and the residual stability of more than 90 percent.
(3) The invention obtains better curing performance on the premise of not influencing the workability of cold-mixed asphalt mixture construction, and the comprehensive pavement performance is excellent.
Detailed Description
The technical solutions of the present invention will be described clearly and completely with reference to the following embodiments of the present invention, and it should be understood that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. All other embodiments, which can be obtained by a person skilled in the art without inventive effort based on the embodiments of the present invention, are within the scope of the present invention.
Example 1
A damp solidified polyurethane modified cold mix asphalt and a preparation method thereof, the steps are as follows:
(1) adding 1 part (by weight, the same below) of Toluene Diisocyanate (TDI) into a reaction kettle, heating to 80 ℃, adding 4 parts of polypropylene glycol with the molecular weight of 1500 into the reaction kettle twice, and stirring and reacting at the temperature of 80 ℃ for 90min to obtain an isocyanate-terminated base-line type polyurethane prepolymer;
(2) adding 70 parts of matrix asphalt into a shearing and stirring kettle, heating to 100 ℃ to completely melt the matrix asphalt, sequentially adding 15 parts of diesel oil, 3 parts of polyethylene wax, 5 parts of polyurethane prepolymer and 1 part of calcium chloride drying agent, and shearing and mixing at the speed of 1500r/min for 90min to obtain polyurethane modified cold-mix asphalt;
(3) and cooling the polyurethane modified cold-mixed asphalt to 70 ℃, adding 2 parts of sulfur powder stabilizer and 0.5 part of methyl isopropyl ketone-polyamide type ketimine curing agent, and shearing and mixing at the speed of 1200r/min for 60min to obtain the damp cured polyurethane modified cold-mixed asphalt.
Example 2
A damp solidified polyurethane modified cold mix asphalt and a preparation method thereof, the steps are as follows:
(1) adding 2 parts of diphenylmethane diisocyanate (MDI) into a reaction kettle, heating to 90 ℃, adding 8 parts of ethylene glycol-propylene glycol-ethylene glycol triblock copolymer with the molecular weight of 2000 into the reaction kettle twice, and stirring and reacting at the temperature of 90 ℃ for 60min to obtain an isocyanate-terminated base-line type polyurethane prepolymer;
(2) adding 75 parts of matrix asphalt into a shearing and stirring kettle, heating to 120 ℃ to completely melt the matrix asphalt, sequentially adding 20 parts of 200# solvent oil, 2 parts of dioctyl phthalate, 10 parts of polyurethane prepolymer and 4 parts of magnesium sulfate drying agent, and shearing and mixing at the speed of 2000r/min for 60min to prepare polyurethane modified cold-mix asphalt;
(3) and cooling the polyurethane modified cold-mixed asphalt to 80 ℃, adding 3 parts of cellulose stabilizer and 1.0 part of acetophenone-polyether amine type ketimine curing agent, and shearing and mixing at the speed of 1500r/min for 30min to obtain the damp cured polyurethane modified cold-mixed asphalt.
Example 3
A damp solidified polyurethane modified cold mix asphalt and a preparation method thereof, the steps are as follows:
(1) adding 3 parts of Hexamethylene Diisocyanate (HDI) into a reaction kettle, heating to 70 ℃, adding 12 parts of polytetrahydrofuran ether glycol with the molecular weight of 1200 into the reaction kettle for three times, and stirring and reacting for 120min at the temperature of 70 ℃ to prepare an isocyanate-terminated base-line type polyurethane prepolymer;
(2) adding 60 parts of matrix asphalt into a shearing and stirring kettle, heating to 90 ℃ to completely melt the matrix asphalt, sequentially adding 10 parts of 180# solvent oil, 5 parts of sasobit resin, 15 parts of polyurethane prepolymer and 3 parts of quicklime drying agent, and shearing and mixing at the speed of 1000r/min for 120min to prepare polyurethane modified cold-mixed asphalt;
(3) and cooling the polyurethane modified cold-mixed asphalt to 60 ℃, adding 1 part of rubber oil stabilizer and 1.5 parts of acetophenone-m-phenylenediamine ketimine curing agent, and shearing and mixing at the speed of 800r/min for 90min to prepare the damp-cured polyurethane modified cold-mixed asphalt.
Comparative example 1
Adding 60 parts of matrix asphalt into a shearing and stirring kettle, heating to 90 ℃ to completely melt the matrix asphalt, sequentially adding 10 parts of 180# solvent oil, 5 parts of sasobit resin, 15 parts of commercially available polyurethane adhesive and 3 parts of quicklime drying agent, and shearing and mixing at the speed of 1000r/min for 120 min. And cooling the system to 60 ℃, adding 1 part of rubber oil stabilizer and 1.5 parts of acetophenone-m-phenylenediamine ketimine curing agent, and shearing and mixing at the speed of 800r/min for 90min to prepare the conventional polyurethane modified cold-mix asphalt.
Comparative example 1 the same materials and process conditions were used as in example 3, except that a commercially available polyurethane glue was used instead of the synthesized isocyanate-terminated base polyurethane prepolymer.
Comparative example 2
Adding 60 parts of matrix asphalt into a shearing and stirring kettle, heating to 90 ℃ to completely melt the matrix asphalt, sequentially adding 10 parts of 180# solvent oil, 5 parts of sasobit resin, 15 parts of commercially available polyurethane adhesive and 3 parts of quicklime drying agent, and shearing and mixing at the speed of 1000r/min for 120 min. And cooling the system to 60 ℃, adding 1 part of rubber oil stabilizer, and shearing and mixing at the speed of 800r/min for 90min to obtain the conventional polyurethane modified cold-mix asphalt.
Comparative example 2 the same materials and process conditions were used as in example 3, except that a commercially available polyurethane glue was used instead of the synthetic isocyanate-terminated base-line polyurethane prepolymer and no ketimine moisture curing agent was added to the process.
The wet cured polyurethane modified cold-mix asphalt obtained in the example 1-3 and the conventional polyurethane modified cold-mix asphalt obtained in the comparative example 1-2 were mixed with aggregate according to the aggregate formula LB-16 of the cold patch asphalt mixture in the technical Specification for road asphalt pavement construction, and the asphalt-aggregate ratio was 6.0%, to obtain a cold-mix asphalt mixture.
And detecting the rotational viscosity and the bonding strength of the cold-mixed asphalt according to JTG E20-2011 test procedures for road engineering asphalt and asphalt mixtures and JGJ/T110-2017 inspection standards for bonding strength of facing bricks in construction engineering. The stability and the residual stability of the cold-mixed asphalt mixture are detected according to JT/T972-2015 Bituminous pavement pit cold-patch finished product, and the detection results are shown in Table 1.
TABLE 1 results of testing the properties of examples and comparative examples
The moisture-cured polyurethane modified cold-mix asphalt prepared in examples 1-3 had low viscosity and bonding strength when uncured, and was beneficial to mixing and paving cold-mix asphalt mixtures. After the cold-mixed asphalt is paved, the wet curing agent and moisture in the cold-mixed asphalt are subjected to reverse reaction to generate an amine chain extender, the polyurethane prepolymer is induced to be crosslinked and cured, the viscosity and the bonding strength of the cold-mixed asphalt are greatly increased, and the stability of the mixture and the stability of the residue are superior to those of a comparative example. The moisture-cured polyurethane modified cold-mixed asphalt can accelerate the formation of the strength of cold-mixed asphalt pavement and meet the requirement of quick traffic of cold-mixed asphalt roads.
The above description is only for the purpose of illustrating the preferred embodiments of the present invention and is not to be construed as limiting the invention, and any modifications, equivalents, improvements and the like that fall within the spirit and principle of the present invention are intended to be included therein.
Claims (10)
1. The moisture-cured polyurethane modified cold-mix asphalt is characterized by comprising the following raw materials in parts by weight: 60-75 parts of matrix asphalt, 10-20 parts of solvent, 5-15 parts of polyurethane prepolymer, 2-5 parts of plasticizer, 1-4 parts of drying agent, 1-3 parts of stabilizer and 0.5-1.5 parts of moisture curing agent.
2. The moisture curing polyurethane modified cold mix asphalt of claim 1, wherein: the polyurethane prepolymer is an isocyanate-terminated base-line polymer synthesized by polyether diol and diisocyanate.
3. The moisture curing polyurethane modified cold mix asphalt of claim 1, wherein: the plasticizer is at least one of polyethylene wax, chlorinated paraffin, sasobit resin, ethylene vinyl acetate or dioctyl phthalate.
4. The moisture curing polyurethane modified cold mix asphalt of claim 1, wherein: the drying agent is at least one of calcium sulfate, magnesium sulfate, calcium chloride or quicklime; the moist curing agent is ketimine; the stabilizer is at least one of sulfur powder, rubber oil, cellulose or lignin.
5. The moisture curing polyurethane modified cold mix asphalt of claim 1, wherein: the matrix asphalt is 70# petroleum asphalt, the penetration degree is 50-70mm (25 ℃), the softening point is 45-55 ℃, and the ductility is more than 100cm (15 ℃); the solvent is at least one of kerosene, diesel oil, 180# solvent oil or 200# solvent oil.
6. The moisture curing polyurethane modified cold mix asphalt of claim 1, wherein: the cold-mixed asphalt is stored in a vacuum sealing way, stirred and paved at normal temperature/low temperature, the formation of the cold-mixed asphalt pavement strength is accelerated, the Marshall stability is 7.7-8.6KN, and the residual stability is more than 90%.
7. The method for preparing the wet curing polyurethane modified cold mix asphalt of any one of claims 1 to 6, which is characterized by comprising the following steps:
(1) adding the matrix asphalt into a shearing and stirring kettle, heating to completely melt the matrix asphalt, sequentially adding a solvent, a plasticizer, a polyurethane prepolymer and a drying agent, and shearing and mixing to obtain polyurethane modified cold-mix asphalt;
(2) and cooling the polyurethane modified cold-mixed asphalt to 60-80 ℃, adding a stabilizer and a moisture curing agent, and shearing and mixing to obtain the moisture cured polyurethane modified cold-mixed asphalt.
8. The method of claim 7, wherein: in the step (1), the matrix asphalt is heated to 90-120 ℃ to be completely melted, the speed of shearing and mixing is 1000-2000r/min, and the time is 60-120 min; the speed of the shearing and mixing in the step (2) is 800-1500r/min, and the time is 30-90 min.
9. The method according to claim 7, wherein the polyurethane prepolymer in the step (1) is prepared as follows: adding diisocyanate into a reaction kettle, heating to 70-90 ℃, keeping the diisocyanate slightly excessive, adding polyether glycol into the reaction kettle for 2-3 times, keeping the temperature at 70-90 ℃, and stirring for reaction for 60-120min to obtain the isocyanate-terminated base-line type polyurethane prepolymer.
10. The method of claim 9, wherein: the polyether diol is one or the combination of a plurality of polypropylene glycol, polytetrahydrofuran ether glycol, ethylene glycol-propylene glycol-ethylene glycol triblock copolymer or polyoxyethylene glycol, the hydroxyl value is 60-120mg KOH/g, and the molecular weight is 1200-2000; the diisocyanate is one or a combination of several of toluene diisocyanate, hexamethylene diisocyanate, diphenylmethane diisocyanate or dicyclohexylmethane diisocyanate.
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CN114292526A (en) * | 2022-01-13 | 2022-04-08 | 同路达(青岛)生态科技有限公司 | Thermosetting polyurethane modified asphalt and preparation method thereof |
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