CN100582161C - Epoxy resin composition and using method thereof - Google Patents
Epoxy resin composition and using method thereof Download PDFInfo
- Publication number
- CN100582161C CN100582161C CN200710021661A CN200710021661A CN100582161C CN 100582161 C CN100582161 C CN 100582161C CN 200710021661 A CN200710021661 A CN 200710021661A CN 200710021661 A CN200710021661 A CN 200710021661A CN 100582161 C CN100582161 C CN 100582161C
- Authority
- CN
- China
- Prior art keywords
- category
- epoxy resin
- add
- hours
- resin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000003822 epoxy resin Substances 0.000 title claims abstract description 41
- 229920000647 polyepoxide Polymers 0.000 title claims abstract description 41
- 239000000203 mixture Substances 0.000 title claims description 45
- 238000000034 method Methods 0.000 title claims description 17
- 229920005989 resin Polymers 0.000 claims abstract description 49
- 239000011347 resin Substances 0.000 claims abstract description 49
- 239000000463 material Substances 0.000 claims abstract description 33
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 30
- 239000004568 cement Substances 0.000 claims abstract description 11
- 239000004593 Epoxy Substances 0.000 claims description 46
- 238000012856 packing Methods 0.000 claims description 25
- 238000003756 stirring Methods 0.000 claims description 19
- 230000000903 blocking effect Effects 0.000 claims description 18
- 238000012360 testing method Methods 0.000 claims description 18
- 238000007599 discharging Methods 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 10
- 239000007822 coupling agent Substances 0.000 claims description 10
- 239000013530 defoamer Substances 0.000 claims description 10
- 238000001816 cooling Methods 0.000 claims description 8
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims description 8
- 239000006229 carbon black Substances 0.000 claims description 7
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 7
- 239000011353 cycloaliphatic epoxy resin Substances 0.000 claims description 7
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 6
- 239000002390 adhesive tape Substances 0.000 claims description 6
- 229920001577 copolymer Polymers 0.000 claims description 6
- 229920002635 polyurethane Polymers 0.000 claims description 6
- 239000004814 polyurethane Substances 0.000 claims description 6
- 238000010792 warming Methods 0.000 claims description 6
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 239000011863 silicon-based powder Substances 0.000 claims description 5
- HJIGCDGIVYPLOK-UHFFFAOYSA-N 2-butoxycarbonylprop-2-enoic acid Chemical compound CCCCOC(=O)C(=C)C(O)=O HJIGCDGIVYPLOK-UHFFFAOYSA-N 0.000 claims description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims description 3
- FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 claims description 3
- YFQPJCUYATWTLO-UHFFFAOYSA-N [4-(oxiran-2-ylmethoxymethyl)cyclohexyl]methanol Chemical compound C1CC(CO)CCC1COCC1OC1 YFQPJCUYATWTLO-UHFFFAOYSA-N 0.000 claims description 3
- 229960004217 benzyl alcohol Drugs 0.000 claims description 3
- 235000019445 benzyl alcohol Nutrition 0.000 claims description 3
- QLBRROYTTDFLDX-UHFFFAOYSA-N [3-(aminomethyl)cyclohexyl]methanamine Chemical compound NCC1CCCC(CN)C1 QLBRROYTTDFLDX-UHFFFAOYSA-N 0.000 claims description 2
- 238000005984 hydrogenation reaction Methods 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 abstract description 12
- 238000010276 construction Methods 0.000 abstract description 9
- 239000000049 pigment Substances 0.000 abstract description 3
- 238000011049 filling Methods 0.000 abstract description 2
- 239000004615 ingredient Substances 0.000 abstract 1
- 239000002075 main ingredient Substances 0.000 abstract 1
- 230000005855 radiation Effects 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- 238000012797 qualification Methods 0.000 description 36
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 24
- -1 alicyclic glycidyl ester Chemical class 0.000 description 21
- 230000002159 abnormal effect Effects 0.000 description 16
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 239000000126 substance Substances 0.000 description 8
- 230000000007 visual effect Effects 0.000 description 8
- 230000032683 aging Effects 0.000 description 7
- 150000001412 amines Chemical group 0.000 description 7
- 230000008859 change Effects 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 238000004382 potting Methods 0.000 description 7
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 6
- YSUQLAYJZDEMOT-UHFFFAOYSA-N 2-(butoxymethyl)oxirane Chemical compound CCCCOCC1CO1 YSUQLAYJZDEMOT-UHFFFAOYSA-N 0.000 description 5
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 5
- 125000002723 alicyclic group Chemical group 0.000 description 5
- 229920001971 elastomer Polymers 0.000 description 5
- 230000010412 perfusion Effects 0.000 description 5
- 239000005060 rubber Substances 0.000 description 5
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 5
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 4
- 229910021630 Antimony pentafluoride Inorganic materials 0.000 description 4
- 230000005856 abnormality Effects 0.000 description 4
- VBVBHWZYQGJZLR-UHFFFAOYSA-I antimony pentafluoride Chemical compound F[Sb](F)(F)(F)F VBVBHWZYQGJZLR-UHFFFAOYSA-I 0.000 description 4
- 230000006835 compression Effects 0.000 description 4
- 238000007906 compression Methods 0.000 description 4
- 230000007547 defect Effects 0.000 description 4
- 230000003628 erosive effect Effects 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 4
- 238000010008 shearing Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000003365 glass fiber Substances 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 238000012423 maintenance Methods 0.000 description 3
- 239000003607 modifier Substances 0.000 description 3
- 239000004570 mortar (masonry) Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 239000004408 titanium dioxide Substances 0.000 description 3
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- OKIZCWYLBDKLSU-UHFFFAOYSA-M N,N,N-Trimethylmethanaminium chloride Chemical compound [Cl-].C[N+](C)(C)C OKIZCWYLBDKLSU-UHFFFAOYSA-M 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 239000004902 Softening Agent Substances 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 150000004982 aromatic amines Chemical class 0.000 description 2
- 239000004567 concrete Substances 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- PDXRQENMIVHKPI-UHFFFAOYSA-N cyclohexane-1,1-diol Chemical compound OC1(O)CCCCC1 PDXRQENMIVHKPI-UHFFFAOYSA-N 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 229940015043 glyoxal Drugs 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 235000012204 lemonade/lime carbonate Nutrition 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229920003986 novolac Polymers 0.000 description 2
- 229920005906 polyester polyol Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- MNAHQWDCXOHBHK-UHFFFAOYSA-N 1-phenylpropane-1,1-diol Chemical compound CCC(O)(O)C1=CC=CC=C1 MNAHQWDCXOHBHK-UHFFFAOYSA-N 0.000 description 1
- AYHLPQOWRMPEKH-UHFFFAOYSA-N 2-(6-methylheptoxymethyl)oxirane Chemical compound CC(C)CCCCCOCC1CO1 AYHLPQOWRMPEKH-UHFFFAOYSA-N 0.000 description 1
- CYCBPQPFMHUATH-UHFFFAOYSA-N 4-(oxiran-2-ylmethoxy)butan-1-ol Chemical compound OCCCCOCC1CO1 CYCBPQPFMHUATH-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229920002121 Hydroxyl-terminated polybutadiene Polymers 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 238000006845 Michael addition reaction Methods 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920004935 Trevira® Polymers 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 229940059260 amidate Drugs 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 230000002929 anti-fatigue Effects 0.000 description 1
- 229920005601 base polymer Polymers 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical group C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 210000000481 breast Anatomy 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 238000013036 cure process Methods 0.000 description 1
- IZRBAWXNLPBYKE-UHFFFAOYSA-N cyclohexane dioctyl benzene-1,2-dicarboxylate Chemical compound C(C=1C(C(=O)OCCCCCCCC)=CC=CC1)(=O)OCCCCCCCC.C1CCCCC1 IZRBAWXNLPBYKE-UHFFFAOYSA-N 0.000 description 1
- YMHQVDAATAEZLO-UHFFFAOYSA-N cyclohexane-1,1-diamine Chemical compound NC1(N)CCCCC1 YMHQVDAATAEZLO-UHFFFAOYSA-N 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000013016 damping Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000006253 efflorescence Methods 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- NPUKDXXFDDZOKR-LLVKDONJSA-N etomidate Chemical compound CCOC(=O)C1=CN=CN1[C@H](C)C1=CC=CC=C1 NPUKDXXFDDZOKR-LLVKDONJSA-N 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 210000004209 hair Anatomy 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 230000016507 interphase Effects 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 125000005375 organosiloxane group Chemical group 0.000 description 1
- 229940059574 pentaerithrityl Drugs 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 150000004714 phosphonium salts Chemical class 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- AZIQALWHRUQPHV-UHFFFAOYSA-N prop-2-eneperoxoic acid Chemical compound OOC(=O)C=C AZIQALWHRUQPHV-UHFFFAOYSA-N 0.000 description 1
- 206010037844 rash Diseases 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000003469 silicate cement Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229960001866 silicon dioxide Drugs 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Landscapes
- Sealing Material Composition (AREA)
- Epoxy Resins (AREA)
Abstract
This invention supply a epoxide resin combination and its preparation method, and its application as filling material of railway plate type orbit convex shape block platform. It takes ethoxyline resin, pigment, padding, curing agent and other accessory ingredient as main ingredient. This ethoxyline resin combination possess good construction usability, good cement bond property, appropriate elasticity and syntheses mechanical property, and has performance of ultraviolet radiation proof, moisture-proof.
Description
Technical field
The present invention relates to a kind of chemical materials, and preparation method thereof with its using method, especially a kind of composition epoxy resin, and preparation method thereof with its using method.
Background technology
Railway particularly the development of high-speed railway be solve that the national economy high speed development sharply increases logistics, the stream of people and energy shortage between contradiction, reduce the effective way of transportation cost, but along with train running speed improves constantly, the ballast aggregate efflorescence of ballasted track and the speed of railway roadbed accumulated deformation are accelerated thereupon, must satisfy the requirement of high-speed railway to circuit high ride, high stability by track structure reinforcement and frequent maintenance work.Compare with ballasted track, ballastless track has the significantly outstanding advantage of minimizing of trajectory stability, rigidity homogeneity and good endurance, ride comfort height, maintenance load.Therefore, from the early sixties in last century, the countries in the world railway is carried out with monoblock type in succession or is solidified the systematic study that railway roadbed substitutes all kinds of ballastless track structures of bulk solid ballast aggregate, and some countries have popularized ballastless track in an all-round way and used as the main track structure pattern of high-speed railway.
On high-speed railway, use ballastless track, with Japan, Germany is the most extensive.Wherein Japanese the Shinkansen plate-type slag-free orbit pattern be up to now working time the longest, lay the longest plate-type slag-free orbit of mileage.China's ballastless track construction last century the nineties begin design and build with test, it is the dog river grand bridge (straight line) of 741m and two what grand bridge (curve) examination bed board formula track that length is 740m that Qinhuangdao Shenyang Special Passenger Line in 1999 is selected length, in the June, 2003 and the end of the year 2003 are again in the examination shop of having carried out slab track in No. 2 tunnels of cobble mouth, bosom, Chongqing, finish the construction of the line 13.6km ballastless track comprehensive test section that changes then the end of the year 2006, and carried out the operation that is open to traffic of speed per hour 250km, open new page on the railway construction in China history.
Plate-type slag-free orbit is made up of ready-formed track plate, concrete bed and marginal CA filled with mortar layer, establishes convex blocking platform between 2 blocks of track plates.For slab track, the concrete convex blocking platform that the track plate is played position-limiting action directly bears longitudinal force and the transverse force that is delivered to sub rail foundation by rail, comprising: the longitudinal force that the interphase interaction of beam rail produces, the track plate contractility that temperature variation causes, horizontal drag, starting and the damping force of track, the horizontal force between wheel track etc.Except above-mentioned mechanical effect, the packing material around the convex blocking platform, also need bear expose to the sun and rain, stress that environment such as ultraviolet ray produces is with aging, easier destruction.Because the complicacy of convex blocking platform Working environment and to the diversity of performance requriements, require its packing material under condition of different temperatures, all cement structures spare to be had good cohesiveness, with transmitted load, and have suitable elasticity and do not produce big deformation and cracking to bear the external force effect.In addition, under all temps condition, must consider that also it uses manufacturability, but suitable working viscosity and usage period and curing speed, more than every performance requriements do not obtain in the prior art satisfying well.Packing material around the convex blocking platform, what Japan adopted in early days is the CA mortar, through having disrepair phenomenon after the operation after a while, use the synthetic resins material substitution CA mortar of intensity height, elasticity and good endurance afterwards instead, used synthetic resins mainly is urethane resin.
Though it is urethane resin has favorable elasticity and splitting resistance as the convex blocking platform potting resin, not so good to the bond effect of cement.The more scabrous processing performance that is to use operation will be reacted generation CO because urethane resin, is met water to water vapor sensitive
2, a large amount of bubbles appear easily, influence the compactness and the homogeneity of potting resin.In the open air under the execution conditions, can not use heating cure shelter isocyanate and can only be in ambient cure, the cement product is difficult to drying, steam is difficult to get rid of, and brings very big difficulty to construction.In order to reduce the generation of bubble, often promotor is quickened gel and the solidified way realizes by adding, but the promotor add-on also is difficult to hold, and it is bigger that its consumption is influenced by temperature, add-on very little, then set time is long, foaming is serious, and add-on has little time to use with regard to gel at most.
Except that urethane resin, also can adopt the packing material of Resins, epoxy as the plate-type slag-free orbit convex blocking platform.Compare with urethane resin, it uses manufacturability and all more excellent to the cohesive force of cement, but the ordinary epoxy resin cured article is more crisp hard, Young's modulus is too high, does not meet retaining platform packing material and has certain elastic requirement, though can produce certain elasticity by adding softening agent or toughner, but as time passes, softening agent or toughner may be moved to the surface owing to itself do not participate in curing reaction, and resin becomes fragility again.
In addition, contain the two keys of a large amount of phenyl ring in common polyurethane resin and the ordinary epoxy resin molecular structure, can cause chain rupture under long-term uviolizing, cause resin-oatmeal to melt and split, bring hidden danger for railway operation steady in a long-term, maintenance cost increases.
Summary of the invention
Goal of the invention: technical problem to be solved by this invention is the deficiency at above-mentioned two kinds of potting resins, a kind of composition epoxy resin is provided, packing material as railway plate-type slag-free orbit convex blocking platform, fully satisfy over-all properties requirements such as the stronger cement-bonded property of packing material, suitable elasticity and compressive strength, ageing-resistant, antifatigue, and has good construction technology performance, can satisfy different weather condition, the requirement of different construction operating modes.
Another technical problem to be solved by this invention provides the preparation method of above-mentioned composition epoxy resin.
The technical problem that the present invention also will solve provides the using method of above-mentioned composition epoxy resin as the packing material of railway plate-type slag-free orbit convex blocking platform.
Technical scheme: the present invention is that to solve the problems of the technologies described above the technical scheme that is adopted as follows:
A kind of composition epoxy resin, said composition divide A, B two classes to pack respectively, and the category-A material is counted composed of the following components by weight: 100 parts of Resins, epoxy, 1~10 part of pigment, 0~300 part of filler, 0~100 part of activity or non-activated thinner, 0~50 part of active or nonactive toughner, 0~5 part of UV light absorber, 0~5 part in oxidation inhibitor, 0~2 part of flow agent, 0~2 part of defoamer, 0~5 part of coupling agent, 0~10 part of fiber reinforced material; The category-B material is a solidifying agent; And the mass ratio of A and B is 20: 1~1: 1.
Resins, epoxy wherein is saturated or unsatured epoxy resin, comprises one or more the mixture in the modifier of alicyclic Racemic glycidol ether type epoxy, alicyclic glycidyl ester type epoxy resin, aliphatic glycidyl ether type Resins, epoxy, aliphatic glycidyl ester type epoxy resin, aromatic glycidyl ether type Resins, epoxy, aromatic series glycidyl ester type epoxy resin and above-mentioned Resins, epoxy.Alicyclic Racemic glycidol ether type epoxy such as Hydrogenated Bisphenol A (F) cyclohexanediol, cyclohexanediol substituent tetraglycidel ether epoxy resin, alicyclic glycidyl ester type epoxy resin such as hexahydrobenzene dioctyl phthalate and substituent ethylene oxidic ester epoxy resin thereof, aliphatics two or polyglycidyl ether (ester) type Resins, epoxy such as tetramethylolmethane glycidyl ether or TriMethylolPropane(TMP) tetraglycidel ether epoxy resin, aromatic glycidyl ether (ester) type Resins, epoxy is typical in lower molecular weight dihydroxyphenyl propane (F) tetraglycidel ether epoxy resin, novolac epoxy etc.The Racemic glycidol ether type resin and the modifier thereof of preferred saturated six-ring, its cured product have certain elasticity, good UV resistant irradiation and chemical resistance.
Above-mentioned modified epoxy is for having introduced rubber structure or polyether segment on the Resins, epoxy molecular chain, can make by following preparation method: in a kind of Resins, epoxy or multiple epoxy resin composition, add the properties-correcting agent that accounts for weight epoxy 0.1~100%, add the catalyzer that accounts for weight epoxy 0~5% again, reacted 0.5~5 hour down at 50~180 ℃.Wherein properties-correcting agent is liquid state end carboxyl or carboxylated nbr, end carboxyl or hydroxyl polybutadiene rubber, end carboxyl or the hydroxy acrylate rubber of molecular weight 1000~10000, or molecular weight is 200~2000 polyoxytrimethylene, polyoxyethylene or polyester polyol, or the mixture of several materials in the above-mentioned properties-correcting agent.Wherein catalyzer be Lewis acid, tertiary amine, imidazoles, quaternary amine or season phosphonium salt, for example benzyldimethylamine, triethylamine, glyoxal ethyline, tetramethyl ammonium chloride, triphenylphosphine, halo triphenylphosphine etc.
This convex blocking platform packing material can be the Resins, epoxy of single variety or the Resins, epoxy of modification, also can be the mixture of several different rings epoxy resins, and is more comprehensive with multiple Resins, epoxy matching property.Resins, epoxy and modified epoxy room temperature are liquid, and epoxy equivalent (weight) is 100~2000g/mol, preferred 200~500g/mol, and viscosity is 100~100000mpa.s25 ℃, preferred 1000~20000mpa.s25 ℃.
Above-mentioned composition epoxy resin, wherein pigment is carbon black or titanium dioxide.
Above-mentioned composition epoxy resin, wherein filler is silicon-dioxide, aluminium sesquioxide or lime carbonate, can also add short glass fiber or polymeric amide, trevira.The effect that adds filler also can be played the effect of the volumetric shrinkage that reduces the epoxy resin cure process except that the production cost that reduces composition epoxy resin, bat wool also can be used as framework material in composition strengthens, and prevents that cracking from appearring in composition epoxy resin in life-time service.Preferred 50~100 parts of filling adding amount, the filler granularity is 100~2000 orders, preferred 200~800 orders.
Above-mentioned composition epoxy resin, wherein reactive thinner and toughner are aliphatics list or polyglycidyl ether, alicyclic list or polyglycidyl ether or aromatic series list or polyglycidyl ether, and non-activated thinner and toughner are phthalic acid ester, low molecular polyether resin.The reactive thinner epoxy equivalent (weight) is 100~2000g/mol, and viscosity is 1~1000mpa.s25 ℃.Non-activated thinner viscosity is 10~1000mpa.s25 ℃.
Above-mentioned composition epoxy resin, wherein UV light absorber is benzophenone analog derivative such as UV531 etc., preferred 0.5~1.5 part of add-on.
Above-mentioned composition epoxy resin, wherein oxidation inhibitor is sterically hindered phenol or phosphorous acid ester, preferred 1~2 part of add-on.
Above-mentioned composition epoxy resin, wherein flow agent is acrylate or organo-siloxane base polymer, preferred 0.1~0.5 part of add-on.
Above-mentioned composition epoxy resin, wherein defoamer is the silicane defoamer, preferred 0.1~0.5 part of add-on.
Above-mentioned composition epoxy resin, wherein coupling agent is end amido or epoxy radicals silicone hydride or titanate coupling agent, preferred 1~2 part of add-on.
Above-mentioned composition epoxy resin, wherein fiber reinforced material is the fibrous or netted cloth of organic or inorganic, and wherein the organic fibre strongthener is polyester or tynex, and the inorganic fibre strongthener is glass fibre or carbon fiber.
Above-mentioned composition epoxy resin, wherein solidifying agent is one or more the mixture in amine curing agent and the modified amine curing agent.Amine curing agent is alicyclic amine solidifying agent, aliphatics amine solidifying agent, aromatic amine solidifying agent.Alicyclic amine solidifying agent comprises different Buddhist diketone diamines (IPDA), cyclohexanediamine.Aliphatics amine solidifying agent comprises diethylenetriamine, Triethylenetetramine (TETA), polyethylene polyamine.The aromatic amine solidifying agent comprises mphenylenediamine, m-xylene diamine.The method of modifying of above-mentioned amine curing agent comprise with the epoxide addition, with the Michael addition of unsaturated double-bond, with saturated or unsaturated monobasic or polycarboxylic acid amidate action and with the Manny base addition of phenolic compound.Preferred alicyclic or aliphatics amine solidifying agent and modifier thereof of solidifying agent wherein, its cured article has better weather.Modified amine curing agent reactive hydrogen equivalent is 20~400g/mol, preferred 50~200g/mol, and viscosity is 10~100000mpa.s25 ℃, preferred 200~20000mpa.s25 ℃.
Above-mentioned composition epoxy resin, its preparation method is: under 5~180 ℃, under 10~3000 rev/mins of stirring velocitys, category-A material all components was mixed 0.1~10 hour, the packing back is as category-A; Amine curing agent packing back is as category-B.In the actual production, available enamel reaction stirring tank, stainless steel reaction stirring tank, high speed dispersor or three-roll grinder mix category-A material all components, and the packing back is as category-A.Preferred high speed dispersor mixes, and also can mix earlier at reaction stirring tank or high speed dispersor, disperses then better effects if at three-roll grinder then.
Above-mentioned composition epoxy resin, its using method as the packing material of railway plate-type slag-free orbit convex blocking platform may further comprise the steps:
1, the preparation before the perfusion: foreign material such as the rubbish around the removing shelves platform, sand, mud, dry moisture with dried cloth.Around convex retaining platform, the blown polyurethane materials that prevents resin leakage is set below the track plate.Paste demoulding adhesive tape on the polyurathamc template of using in the side, be unlikely to be bonded on the template after making resin solidification.
2, the stirring of resin with mix: the category-A material is fully stirred (can select the hand electric stirrer for use), adds the category-B material then, mix to stir and to make it to mix in 5~15 minutes.When very fast, should pour out another container of part packing as the high heat release of temperature, and in the water cooling of container appearance.In stirring construction operation, should avoid sneaking into water (will influence condensate performance), can operation after in used container, facility, all will getting rid of moisture.Sleety weather should stop construction.
3, resin dosing equipment: should guarantee during perfusion that the template periphery of setting up around the convex retaining platform seals, and does not have and leaks.For making convex retaining platform track plate on every side not be subjected to resin stain, should cover with polyethylene film.Should be slowly during perfusion, inject continuously, prevent to bring into air, guarantee that perfusion is closely knit, until perfusion till keep off platform and be full of.
4, the demoulding and aftertreatment: be cured under the room temperature condition, generally in external temperature more than 20 ℃, pouring into after 7~8 hours is collapsible die.Wiped by the available acetone in the dirty place of resin after the demoulding, cured portion is wiped off with cutter, and cleaning is clean.
Beneficial effect: the invention provides a kind of composition epoxy resin that is used for railway plate-type slag-free orbit convex blocking platform packing material, said composition has bonds well power, good UV resistant irradiation, wet and heat ageing resistant, resistance to chemical attack to cement components, and have certain elasticity and physical strength, it is the compaction material of the convex blocking platform of at present more excellent railway plate-type slag-free orbit, and the preparation method of said composition is simple to operate, is easy to industrialization.
Embodiment
The invention will be further described below by embodiment.
Embodiment 1:
In the high speed dispersor mixing tank, drop into alicyclic Racemic glycidol ether type epoxy JEw-0120 (Changshu good send out chemical company limited produce) 100g, glycidyl ether type snappiness Resins, epoxy (DOW CEMIACAL DER755) 20g, hexylene glycol Racemic glycidol ether type epoxy (Changshu good send out chemical the JX-025 of company limited) 1.3g, carbon black 2g, active micro silicon powder HGH600 50g, HGH1000 20g, defoamer A-530 (German Bi Ke chemistry) 0.1g, coupling agent KH-560 1g, 1000~1600 rev/mins of rotating speeds, 25~40 ℃ were stirred 1 hour down, then mixture is poured into there-necked flask at 80~100 ℃ ,-0.1MPa deaeration was stirred 1 hour, and discharging is packed as category-A.
The contrast of table 1 embodiment 1 test result
Sequence number | Project name | The technical qualification requirement | Embodiment 1 | Testing method |
1 | Visual appearance | The surface no significant defect | Smooth smooth, no bubble | Visual |
2 | Volume density g/cm 3 | ≥1.05 | 1.25 | " technical qualification " appendix C |
3 | Cure shrinkage % | ≤10 | 0.5 | |
4 | Ultimate compression strength Mpa | ≥7.5 | 18.06 | " technical qualification " appendix D |
5 | Coefficient of elasticity KN/mm | 10±2 | 9.24 | " technical qualification " appendix E |
6 | Fatigue property | Maximum compressibility below 1.25mm, the outward appearance Non Apparent Abnormality | 0.78mm outward appearance does not have considerable change | " technical qualification " appendix F |
7 | Shearing resistance MPa | ≥1.96 | 3.61 | " skill condition " appendix G |
8 | Bonding strength MPa | ≥0.49 | 3.20 | " technical qualification " appendix H |
9 | Surface hardness (Shao Shi A) | ≥50 | 92 | GB4493 |
10 | Erosion resistance | Outward appearance is no abnormal, and coefficient of elasticity is in ± 20% | Outward appearance is no abnormal, coefficient of elasticity 9.87% | " technical qualification " appendix I |
11 | Heat-proof aging | Outward appearance is no abnormal, and coefficient of elasticity is in ± 20% | Outward appearance is no abnormal, coefficient of elasticity 10.68% | " technical qualification " appendix J |
In 1 liter of there-necked flask, add different Buddhist diketone diamines (IPDA) 340g, stir and be warming up to 60~80 ℃, drip JEw-0120 143g, butylglycidyl ether (BGE) 60g, keep reaction 3~5 hours, add antioxidant 1010 10g, the deaeration discharging is as category-B under the-0.1MPa.
Exsiccant cement retaining platform model is cleaned out, around convex retaining platform, the blown polyurethane materials that prevents resin leakage is set below the track plate, paste demoulding adhesive tape on the polyurathamc template of using in the side.Get above-mentioned category-A 300g, category-B 70g, at room temperature mix and stirred 10~15 minutes, be poured in the retaining platform resin mould, it is 4000~8000mpa.s25 ℃ that A, B mix back viscosity, but 25 ℃ of usage periods are 1 hour, gel time is 2 hours, and be 8 hours first set time, in 25~30 ℃ of self-vulcanizings demoulding in 7 days, test by The Ministry of Railway of the People's Republic of China, MOR's " line plate-type slag-free orbit convex blocking platform potting resin technical qualification then change ", main performance index relatively sees Table 1.
Embodiment 2:
In 1 liter of there-necked flask, add toluene 300g, the polyoxytrimethylene of molecular weight 800~1000 and ethylene oxide copolymer 100g, SbF5 5g, stirring is warming up to 50 ℃, adds cycloaliphatic epoxy resin JEw-0112 100g in 2~3 hours, reacts 1 hour, add tap water 50~100g, wash out except that SbF5, add JEw-0112 200g again, stir and heat up at 130~150 ℃, remove toluene under the-0.1MPa, discharging is filtered in cooling, test epoxy equivalent (weight) 300g/mol, viscosity 12000mpa.s25 ℃.
In the high speed dispersor mixing tank, drop into above-mentioned modified epoxy 200g, add 1,4 butyleneglycol glycidyl ether (Changshu good send out chemical the JX-024 of company limited) 30g, titanium dioxide 20g, HGH400 silicon powder 100g, silicate cement 50g, short glass fiber 15g, flow agent 2g, 570 defoamer 1g, coupling agent KH560 5g, 1000~1600 rev/mins of rotating speeds, 25~40 ℃ were stirred 1 hour down, changed the there-necked flask vacuum defoamation over to and stirred discharging in 1 hour packing as category-A.
In 1 liter of there-necked flask, add different Buddhist diketone diamines (IPDA) 170g, Triethylenetetramine (TETA) 146g, stirring is warming up to 50~80 ℃, drip E-51 Resins, epoxy 76g, iso-octyl glycidyl ether (Changshu good send out chemical the JX-014 of company limited) 310g, keep reaction 3~5 hours, add phenylcarbinol 50g, the deaeration discharging is as category-B under-0.1MPa.
The contrast of table 2 embodiment 2 test results
Sequence number | Project name | The technical qualification requirement | Embodiment 2 | Testing method |
1 | Visual appearance | The surface no significant defect | Smooth smooth, no bubble | Visual |
2 | Volume density g/cm 3 | ≥1.05 | 1.29 | " technical qualification " appendix C |
3 | Cure shrinkage % | ≤10 | 0.8 | |
4 | Ultimate compression strength Mpa | ≥7.5 | 16.06 | " technical qualification " appendix D |
5 | Coefficient of elasticity KN/mm | 10±2 | 8.36 | " technical qualification " appendix E |
6 | Fatigue property | Maximum compressibility below 1.25mm, the outward appearance Non Apparent Abnormality | 0.81mm outward appearance does not have considerable change | " technical qualification " appendix F |
7 | Shearing resistance MPa | ≥1.96 | 3.89 | " skill condition " appendix G |
8 | Bonding strength MPa | ≥0.49 | 3.32 | " technical qualification " appendix H |
9 | Surface hardness (Shao Shi A) | ≥50 | 90 | GB4493 |
10 | Erosion resistance | Outward appearance is no abnormal, and coefficient of elasticity is in ± 20% | Outward appearance is no abnormal, coefficient of elasticity 8.27 | " technical qualification " appendix I |
11 | Heat-proof aging | Outward appearance is no abnormal, and coefficient of elasticity is in ± 20% | Outward appearance is no abnormal, coefficient of elasticity 9.98 | " technical qualification " appendix J |
Exsiccant cement retaining platform model is cleaned out, around convex retaining platform, the blown polyurethane materials that prevents resin leakage is set below the track plate, paste demoulding adhesive tape on the polyurathamc template of using in the side.Get above-mentioned category-A 300g, category-B 60g, stirred 10~15 fens in mixed at room temperature, be poured in the retaining platform resin mould, it is 6000~9000mpa.s25 ℃ that A, B mix back viscosity, but 25 ℃ of usage periods are 0.8 hour, gel time is 1.5 hours, and be 6 hours first set time, 25~30 ℃ of self-vulcanizing demouldings after 7 days, test by The Ministry of Railway of the People's Republic of China, MOR's " line plate-type slag-free orbit convex blocking platform potting resin technical qualification then change ", salient features relatively sees Table 2.
Embodiment 3:
In 1 liter of there-necked flask, add cycloaliphatic epoxy resin JEw-0122 300g, nbr carboxyl terminal (molecular-weight average 2000) 15g, end carboxy acrylic butyl ester/methylmethacrylate copolymer (molecular-weight average 1500) 30g, 120~160 ℃ were reacted 2 hours, discharging is filtered in cooling, test epoxy equivalent (weight) 232g/mol, viscosity 25000mpa.s25 ℃.
In the high speed dispersor mixing tank, drop into above-mentioned modified epoxy 200g, add 1,4-cyclohexanedimethanol glycidyl ether (Changshu good send out chemical the JX-026 of company limited) 50g, carbon black 10g, HGH600 silicon powder 100g, water-ground limestone (400 order) 50g, flow agent 2g, 570 defoamer 1g, titanate coupling agent 10g.1000~1600 rev/mins of rotating speeds, 25~40 ℃ were stirred 1 hour down, changed the there-necked flask vacuum defoamation over to and stirred discharging in 1 hour packing as category-A.
The contrast of table 3 embodiment 3 test results
Sequence number | Project name | The technical qualification requirement | Embodiment 3 | Testing method |
1 | Visual appearance | The surface no significant defect | Smooth smooth, no bubble | Visual |
2 | Volume density g/cm 3 | ≥1.05 | 1.31 | " technical qualification " appendix C |
3 | Cure shrinkage % | ≤10 | 0.8 | |
4 | Ultimate compression strength Mpa | ≥7.5 | 19.06 | " technical qualification " appendix D |
5 | Coefficient of elasticity KN/mm | 10±2 | 9.25 | " technical qualification " appendix E |
6 | Fatigue property | Maximum compressibility below 1.25mm, the outward appearance Non Apparent Abnormality | 0.67mm outward appearance does not have considerable change | " technical qualification " appendix F |
7 | Shearing resistance MPa | ≥1.96 | 3.49 | " skill condition " appendix G |
8 | Bonding strength MPa | ≥0.49 | 3.12 | " technical qualification " appendix H |
9 | Surface hardness (Shao Shi A) | ≥50 | 95 | GB4493 |
10 | Erosion resistance | Outward appearance is no abnormal, and coefficient of elasticity is in ± 20% | Outward appearance is no abnormal, coefficient of elasticity 9.87 | " technical qualification " appendix I |
11 | Heat-proof aging | Outward appearance is no abnormal, and coefficient of elasticity is in ± 20% | Outward appearance is no abnormal, coefficient of elasticity 10.2 | " technical qualification " appendix J |
In 1 liter of there-necked flask, add hydrogenation m-xylene diamine (1,3BAC) 142g, different Buddhist diketone diamines (IPDA) 85g, stirring is warming up to 50~80 ℃, drip aliphatic glycidyl ether type snappiness Resins, epoxy (DER732) 330g, keep reaction 3~5 hours, add phenylcarbinol 100g, the deaeration discharging is as category-B under pressure-0.1MPa.
Exsiccant cement retaining platform model is cleaned out, around convex retaining platform, the blown polyurethane materials that prevents resin leakage is set below the track plate, paste demoulding adhesive tape on the polyurathamc template of using in the side.Get above-mentioned category-A 300g, category-B 100g, stirred 10~15 fens in mixed at room temperature, be poured in the retaining platform resin mould, it is 7000~10000mpa.s25 ℃ that A, B mix back viscosity, but 25 ℃ of usage periods are 1.2 hours, gel time is 2.5 hours, and be 9 hours first set time, 25~30 ℃ of self-vulcanizing demouldings after 7 days, test by The Ministry of Railway of the People's Republic of China, MOR's " line plate-type slag-free orbit convex blocking platform potting resin technical qualification then change ", the salient features test index relatively sees Table 3.
Embodiment 4:
In 1 liter of there-necked flask, drop into Resins, epoxy DYD128 (bisphenol A type epoxy resin, epoxy equivalent (weight) 189, viscosity 13000mpa.s25 ℃) 200g, add butylglycidyl ether (BGE epoxy equivalent (weight) 175, viscosity 2mpa.s25 ℃) 30g, titanium dioxide 5g, HGH600 silicon powder 100g, water-ground limestone (400 order) 50g, flow agent 1g, 570 defoamer 1g, titanate coupling agent 10g is 1000~1600 rev/mins of rotating speeds, 25~40 ℃ were stirred 1 hour down, discharging is packed as category-A, epoxy equivalent (weight) 400g/mol, viscosity 12000mpa.s.
The contrast of table 4 embodiment 4 test results
Sequence number | Project name | The technical qualification requirement | Embodiment 4 | Testing method |
1 | Visual appearance | The surface no significant defect | A small amount of bubble is arranged | Visual |
2 | Volume density g/cm 3 | ≥1.05 | 1.30 | " technical qualification " appendix C |
3 | Cure shrinkage % | ≤10 | 1.0 | |
4 | Ultimate compression strength Mpa | ≥7.5 | 21.02 | " technical qualification " appendix D |
5 | Coefficient of elasticity KN/mm | 10±2 | 11.1 | " technical qualification " appendix E |
6 | Fatigue property | Maximum compressibility below 1.25mm, the outward appearance Non Apparent Abnormality | 0.58mm outward appearance has hair line | " technical qualification " appendix F |
7 | Shearing resistance MPa | ≥1.96 | 3.89 | " skill condition " appendix G |
8 | Bonding strength MPa | ≥0.49 | 3.32 | " technical qualification " appendix H |
9 | Surface hardness (Shao Shi A) | ≥50 | 96 | GB4493 |
10 | Erosion resistance | Outward appearance is no abnormal, and coefficient of elasticity is in ± 20% | Outward appearance is no abnormal, coefficient of elasticity 11.5 | " technical qualification " appendix I |
11 | Heat-proof aging | Outward appearance is no abnormal, and coefficient of elasticity is in ± 20% | Outward appearance is no abnormal, coefficient of elasticity 14.3 | " technical qualification " appendix J |
Exsiccant cement retaining platform model is cleaned out, around convex retaining platform, the blown polyurethane materials that prevents resin leakage is set below the track plate, paste demoulding adhesive tape on the polyurathamc template of using in the side.Get 100 parts of category-As, solidifying agent (the trade mark 593 that adds category-B butylglycidyl ether and diethylenetriamine modified product, reactive hydrogen equivalent 68g/mol, viscosity 350mpa.s) 17 part, at room temperature mix and stirred 10~15 minutes, in the cast retaining platform resin mould, A, it is 3000~4000mpa.s25 ℃ that B mixes back viscosity, but 25 ℃ of usage periods are 0.5 hour, gel time is 0.8 hour, and be 6 hours first set time, 25~30 ℃ of self-vulcanizing demouldings after 7 days, test by The Ministry of Railway of the People's Republic of China, MOR's " line plate-type slag-free orbit convex blocking platform potting resin technical qualification then change ", salient features relatively sees Table 4.
Embodiment 5:
With embodiment 1 described method, different is at 5~20 ℃, under-0.1~0Mpa pressure, with hexahydrobenzene dioctyl phthalate glycidyl ester resin 100g, carbon black 5g, 600 order aluminium sesquioxide powder 10g, thinner 100g, toughner 10g, UV531 5g, flow agent 2g, defoamer 2g and polymeric amide chopped strand 10g are under 10 rev/mins stirring velocity, mixed 10 hours, the packing back is as category-A.And get category-A 100g, category-B 100g at room temperature stirred 5~10 minutes.
Embodiment 6:
With embodiment 1 described method, different is at 5~10 ℃, under-0.1~0Mpa pressure, with 1,4 cyclohexanedimethanol glycidyl ether resin 100g, carbon black 6g, 600 order aluminium sesquioxide powder 300g, toughner 50g, UV531 3g, flow agent 1g, defoamer 1g and coupling agent 5g are under 200 rev/mins stirring velocity, mixed 0.1 hour, cooling back packing is as category-A.And get category-A 200g, category-B 10g at room temperature stirred 5~10 minutes.
Embodiment 7:
With embodiment 1 described method, different is following, 160~180 ℃ with novolac epoxy F-51 100g, polypropylene glycol glycidyl ether (epoxy equivalent (weight) 300 viscosity 50mpa.s25 ℃) 30g, carbon black 6g, 600 order lime carbonate 100g, toughner 10g, oxidation inhibitor 5g, flow agent 1g and coupling agent 5g are under 100 rev/mins stirring velocity, mixed 5 hours, the packing back is as category-A.
Embodiment 8:
With embodiment 1 described method, different is under 90~100 ℃, and the category-A component under 3000 rev/mins stirring velocity, was mixed 0.1 hour, and cooling back packing is as category-A.
Embodiment 9:
With embodiment 2 described methods, the preparation method of different is modified epoxy is as follows: add toluene 300g, the polyester polyol 0.3g of molecular weight 20~400 in 1 liter of there-necked flask, SbF5 5g, stirring is warming up to 50 ℃, adds cycloaliphatic epoxy resin JEw-0112 100g in 2~3 hours, reacts 4 hours, add tap water 50~100g, wash out except that SbF5, add JEw-0112 200g again, stir and heat up at 150~180 ℃, remove toluene under the-0.1MPa, discharging is filtered in cooling.
Embodiment 10:
With embodiment 3 described methods, the preparation method of different is modified epoxy is as follows: add cycloaliphatic epoxy resin JEw-0122 300g in 1 liter of there-necked flask, hydroxyl terminated polybutadiene rubber (molecular-weight average 10000) 100g, terminal hydroxy group butyl acrylate/methylmethacrylate copolymer (molecular-weight average 1500) 200g, 140~180 ℃ were reacted 0.5 hour, and discharging is filtered in cooling.
Embodiment 11:
With embodiment 3 described methods, the preparation method of different is modified epoxy is as follows: add cycloaliphatic epoxy resin JEw-0122 300g in 1 liter of there-necked flask, carboxyl terminated potybutadiene rubber (molecular-weight average 1000) 100g, end carboxy acrylic butyl ester/methylmethacrylate copolymer (molecular-weight average 5000) 200g, add 15g triethylamine or glyoxal ethyline, 100~120 ℃ of reactions 2 hours.
Embodiment 12:
With embodiment 3 described methods, the preparation method of different is modified epoxy is as follows: add cycloaliphatic epoxy resin JEw-0122 300g in 1 liter of there-necked flask, carboxyl terminated potybutadiene rubber (molecular-weight average 3000) 100g, end carboxy acrylic butyl ester/methylmethacrylate copolymer (molecular-weight average 1000) 200g, add 10g tetramethyl ammonium chloride or triphenylphosphine, 100~120 ℃ of reactions 3 hours.
Claims (2)
1, a kind of composition epoxy resin, it is characterized in that this composition epoxy resin by respectively the packing A, B two classes form, category-A and category-B prepare as follows respectively and get:
In 1 liter of there-necked flask, add cycloaliphatic epoxy resin JEw-0122 300g, the nbr carboxyl terminal 15g of molecular-weight average 2000, the end carboxy acrylic butyl ester/methylmethacrylate copolymer 30g of molecular-weight average 1500,120~160 ℃ were reacted 2 hours, discharging is filtered in cooling, test epoxy equivalent (weight) 232g/mol, viscosity 25000mpa.s25 ℃;
In the high speed dispersor mixing tank, drop into above-mentioned modified epoxy 200g, add 1,4 cyclohexane dimethanol glycidyl ether JX-026 50g, carbon black 10g, HGH600 silicon powder 100g, 400 order water-ground limestone 50g, flow agent 2g, 570 defoamer 1g, titanate coupling agent 10g, 1000~1600 rev/mins of rotating speeds, 25~40 ℃ were stirred 1 hour down, changed the there-necked flask vacuum defoamation over to and stirred discharging in 1 hour packing as category-A;
In 1 liter of there-necked flask, add hydrogenation m-xylene diamine 1,3BAC 142g, isophorone diamine 85g, stirring is warming up to 50~80 ℃, drip aliphatic glycidyl ether type snappiness Resins, epoxy DER732 330g, keep reaction 3~5 hours, add phenylcarbinol 100g, the deaeration discharging is as category-B under pressure-0.1MPa;
Above-mentioned category-A 300g, category-B 100g, packing respectively.
2, the described composition epoxy resin of claim 1 is as the using method of the packing material of railway plate-type slag-free orbit convex blocking platform, it is characterized in that this method is: exsiccant cement retaining platform model is cleaned out, the blown polyurethane materials that prevents resin leakage is set below the track plate around convex retaining platform, pastes demoulding adhesive tape on the polyurathamc template of using in the side; Category-A is mixed with category-B, stirred 10~15 fens in mixed at room temperature, be poured in the retaining platform resin mould, it is 7000~10000mpa.s25 ℃ that A, B mix back viscosity, but 25 ℃ of usage periods are 1.2 hours, gel time is 2.5 hours, and be 9 hours first set time, 25~30 ℃ of self-vulcanizing demouldings after 7 days.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN200710021661A CN100582161C (en) | 2007-04-20 | 2007-04-20 | Epoxy resin composition and using method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN200710021661A CN100582161C (en) | 2007-04-20 | 2007-04-20 | Epoxy resin composition and using method thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
CN101045809A CN101045809A (en) | 2007-10-03 |
CN100582161C true CN100582161C (en) | 2010-01-20 |
Family
ID=38770739
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN200710021661A Active CN100582161C (en) | 2007-04-20 | 2007-04-20 | Epoxy resin composition and using method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN100582161C (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101831146A (en) * | 2010-03-18 | 2010-09-15 | 广州奥锐装饰工程有限公司 | Glass-reinforced plastic repairing agent |
CN102504205A (en) * | 2011-11-10 | 2012-06-20 | 湖南神力铃胶粘剂制造有限公司 | Preparation method for epoxy hardener resistant to boiling water boiling |
Families Citing this family (42)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101402839B (en) * | 2008-11-18 | 2012-05-09 | 广州鹿山新材料股份有限公司 | Adhesive for aluminum honeycomb composite board and preparation method thereof |
CN101560077B (en) * | 2009-05-11 | 2012-08-08 | 常熟佳发化学有限责任公司 | Epoxy resin mortar composite used for plate type fragment-free track |
CN102115653B (en) * | 2009-12-31 | 2013-12-04 | 比亚迪股份有限公司 | Binding agent composition, preparation method and application thereof |
CN101735708B (en) * | 2010-01-12 | 2012-07-25 | 广州飞宇建材科技有限公司 | Anti-ageing epoxy paint, preparation method and application thereof |
CN102190857B (en) * | 2010-03-05 | 2013-03-06 | 上海耐齐建材有限公司 | Solvent-free double-component epoxy moisture-proof film |
CN101880515A (en) * | 2010-06-28 | 2010-11-10 | 深圳市库泰克电子材料技术有限公司 | High-reliability and low-viscosity underfill |
CN101985514B (en) * | 2010-11-03 | 2013-01-30 | 常熟佳发化学有限责任公司 | Thermosetting resin composition and preparation method and using method thereof |
CN102533189B (en) * | 2010-12-16 | 2013-10-02 | 湖北回天胶业股份有限公司 | Wet-heat resisting automobile folding adhesive and preparation method thereof |
CN102250573B (en) * | 2011-05-05 | 2013-01-23 | 北京天山新材料技术股份有限公司 | High shear and high peel strength epoxy adhesive |
US9273177B2 (en) * | 2011-06-08 | 2016-03-01 | Huntsman Advanced Materials Americas Llc | Curing agents providing a low ratio of thin-film cure time to gel time |
CN102408675B (en) * | 2011-08-26 | 2013-06-05 | 郑州大学 | Epoxy resin crack filling material and preparation method thereof |
CN102732201B (en) * | 2012-06-25 | 2014-04-09 | 烟台开发区泰盛精化新材料有限公司 | Wear-resistant and weather-resistant epoxy resin coating adhesive and its preparation method |
CN103790020B (en) * | 2012-10-26 | 2016-06-29 | 中国石油化工股份有限公司 | Epoxy resin sizing agent emulsion that polyurethane structural is modified and preparation thereof and application |
CN102994031B (en) * | 2012-10-31 | 2014-07-02 | 安徽东方金河精密机械制造有限公司 | Epoxy adhesive |
CN103045147B (en) * | 2012-12-21 | 2014-08-13 | 上海康达化工新材料股份有限公司 | Cold-proof and damp-proof epoxy resin main agent for crystal glue drip and preparation method thereof |
CN103224611A (en) * | 2013-05-15 | 2013-07-31 | 程梦喜 | Modified alicyclic amine curing agent and preparation method thereof |
CN103242792A (en) * | 2013-05-24 | 2013-08-14 | 黑龙江省科学院石油化学研究院 | Primer for metal substrate structural bonding and preparation method thereof |
CN103980663B (en) * | 2014-04-08 | 2016-07-06 | 宁波市胜源技术转移有限公司 | A kind of composite for juvenile automobile car body panel and preparation method thereof |
CN104694069B (en) * | 2014-12-31 | 2016-09-28 | 黑龙江省科学院石油化学研究院 | Preparation method of medium-temperature cured cyanate ester foaming structural adhesive |
CN104845040A (en) * | 2015-01-14 | 2015-08-19 | 无锡龙舜实业有限公司 | Preparation process of G-20 type epoxy casting agent |
CN104845041A (en) * | 2015-01-14 | 2015-08-19 | 无锡龙舜实业有限公司 | G-20 type epoxy casting agent |
CN105971368B (en) * | 2016-06-29 | 2019-02-12 | 广西凯威铁塔有限公司 | Manufacturing method of weather-resistant artificial tree bark cement telegraph pole |
CN106121345B (en) * | 2016-06-29 | 2019-02-12 | 广西凯威铁塔有限公司 | Manufacturing method of simulated cement telegraph pole |
CN106010116B (en) * | 2016-06-29 | 2019-02-12 | 广西凯威铁塔有限公司 | Anti-aging artificial tree bark and manufacturing method thereof |
CN106195081B (en) * | 2016-06-29 | 2018-06-08 | 芜湖德业摩擦材料有限公司 | A kind of heat-resisting friction material of brake pad of car Special wear-resistant |
CN106118358B (en) * | 2016-06-29 | 2019-02-12 | 广西凯威铁塔有限公司 | Flame-retardant artificial tree bark and manufacturing method thereof |
CN106182400B (en) * | 2016-06-29 | 2019-02-12 | 广西凯威铁塔有限公司 | Method for manufacturing flame-retardant artificial tree bark cement telegraph pole |
CN106150174B (en) * | 2016-06-29 | 2019-02-22 | 广西凯威铁塔有限公司 | Simulation landscape iron tower |
CN106280263A (en) * | 2016-08-26 | 2017-01-04 | 张海棠 | A kind of cable healant and application thereof |
CN106495614A (en) * | 2016-10-28 | 2017-03-15 | 南京信息工程大学 | A kind of compounding insulating material and preparation method thereof |
CN108070100A (en) * | 2016-11-16 | 2018-05-25 | 上海材料研究所 | A kind of post-processing approach of fiber collaboration epoxy resin enhancing 3D printing part |
CN106653328B (en) * | 2016-12-16 | 2017-12-12 | 广东四会互感器厂有限公司 | Equal laminated structure of terminal of current transformer |
CN108414056B (en) * | 2018-05-10 | 2024-01-12 | 合肥邦立电子股份有限公司 | Be applied to liquid level float and non-contact methyl alcohol level sensor of methyl alcohol |
TWI811384B (en) * | 2018-06-20 | 2023-08-11 | 日商Dic股份有限公司 | Acid group-containing (meth)acrylate resin composition, curable resin composition, cured product, and resin material for solder resist |
CN109722137B (en) * | 2019-02-26 | 2021-02-23 | 成都顺佳美恒新材料有限公司 | Environment-friendly water-based interfacial agent and preparation method thereof |
CN113826195B (en) * | 2019-06-25 | 2025-01-14 | 株式会社村田制作所 | Composite component and method of manufacturing the same |
CN110294920B (en) * | 2019-07-02 | 2021-12-17 | 陕西生益科技有限公司 | High-toughness weather-resistant resin composition and application thereof |
CN112111067A (en) * | 2020-09-24 | 2020-12-22 | 邓会群 | Modified epoxy resin and preparation method thereof, emulsified modified epoxy resin and preparation method and application thereof, and sandwich adhesive for aluminum honeycomb core |
CN113045861A (en) * | 2021-04-07 | 2021-06-29 | 青海宜化化工有限责任公司 | PVCSG soft 5 type resin and production process thereof |
CN113845757B (en) * | 2021-08-24 | 2023-07-18 | 国网河北省电力有限公司电力科学研究院 | A kind of corrosion-resistant high electrical performance resin and preparation method thereof |
CN114316516A (en) * | 2021-12-31 | 2022-04-12 | 广州惠利电子材料有限公司 | Formula and preparation method of toughened epoxy resin |
CN114524655B (en) * | 2022-01-28 | 2022-09-09 | 广东铁科灌浆科技有限公司 | High-strength epoxy polymer modified cement mortar and preparation method thereof |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN85102217A (en) * | 1985-04-01 | 1986-08-06 | 中国科学院长春应用化学研究所 | Fill-sealing material of cable plug for motor submerged in oil |
WO1999003932A1 (en) * | 1997-07-17 | 1999-01-28 | AKEMI Chem.-Techn. Spezialfabrik Erich Höntsch GmbH | Structural filler and structural paste |
CN1818212A (en) * | 2005-12-09 | 2006-08-16 | 中铁八局集团有限公司 | Plated rail without ballast |
-
2007
- 2007-04-20 CN CN200710021661A patent/CN100582161C/en active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN85102217A (en) * | 1985-04-01 | 1986-08-06 | 中国科学院长春应用化学研究所 | Fill-sealing material of cable plug for motor submerged in oil |
WO1999003932A1 (en) * | 1997-07-17 | 1999-01-28 | AKEMI Chem.-Techn. Spezialfabrik Erich Höntsch GmbH | Structural filler and structural paste |
CN1818212A (en) * | 2005-12-09 | 2006-08-16 | 中铁八局集团有限公司 | Plated rail without ballast |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101831146A (en) * | 2010-03-18 | 2010-09-15 | 广州奥锐装饰工程有限公司 | Glass-reinforced plastic repairing agent |
CN102504205A (en) * | 2011-11-10 | 2012-06-20 | 湖南神力铃胶粘剂制造有限公司 | Preparation method for epoxy hardener resistant to boiling water boiling |
CN102504205B (en) * | 2011-11-10 | 2013-06-19 | 湖南神力铃胶粘剂制造有限公司 | Preparation method for epoxy hardener resistant to boiling water boiling |
Also Published As
Publication number | Publication date |
---|---|
CN101045809A (en) | 2007-10-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN100582161C (en) | Epoxy resin composition and using method thereof | |
CN100523084C (en) | Polyurethane resin combination and preparation method and using method thereof | |
CN100547029C (en) | A kind of unsaturated resin composition, and preparation method thereof with its using method | |
CN101985514B (en) | Thermosetting resin composition and preparation method and using method thereof | |
CN101560077B (en) | Epoxy resin mortar composite used for plate type fragment-free track | |
CN101724218B (en) | Unsaturated resin composition as well as preparation method and purpose thereof | |
CN104781302B (en) | Tetramine containing polyethylene for resin transfer moulding method and the epoxy-resin systems of triethylenediamine catalyst | |
CN103482904B (en) | A kind of modified epoxy mortar resistant abrasion patching material | |
CN103554843B (en) | Track is filled, preparation and the construction method of epoxy grouting material for back-grouting | |
CN101735595A (en) | Polyurethane resin composition, preparation method and application thereof | |
CN101805588B (en) | Polyurethane road caulking sealant with good durability and production process | |
CN104781303B (en) | Epoxy-resin systems for the tetramine containing polyethylene of resin transfer moulding method | |
CN102010498B (en) | Method for preparing polyurethane elastomer capable of rapidly expanding when contacting water | |
CN104446134B (en) | Maintaining composition for concrete structural component of slab ballastless track, preparation method and application of maintaining composition | |
CN102924692A (en) | High-permeability polyurethane graft-modified epoxy resin interpenetrating-network polymer grouting material and preparation method thereof | |
CN102020831B (en) | Composite material for wind power generation blades | |
CN110373143A (en) | A kind of road and bridge normal temperature cure flexibilized epoxies water-proof adhesive and preparation method thereof | |
CN109942779A (en) | High-speed rail non-fragment orbit off-seam repairs slurries and preparation method thereof | |
CN105566854A (en) | Epoxy resin composition with special curing characteristics and composite thereof | |
CN101475779A (en) | Photo-setting adhesive for press key bonding injection moulding | |
CN108250899A (en) | A kind of air drying type room temperature-cured aqueous epoxy water-repellent paint and its preparation method and application | |
CN101585956B (en) | Epoxy resin system for casting process of wind electricity generation vanes | |
EP4223718A1 (en) | Slag-containing polymer concrete and grouting mortar | |
CN101602915A (en) | Polyurethane water-proof paint of environment-friendly and high-performance inierpeneirating network structure and preparation method thereof | |
CN103087667B (en) | A kind of Polyurethane ballast glue and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
TR01 | Transfer of patent right |
Effective date of registration: 20200102 Address after: 313309 modern industrial park, Emperor lake, Anji County, Zhejiang, Huzhou Patentee after: Hang Mo New Material Group Co., Ltd. Address before: 215553 the Fuchun River Road, Southeast Development Zone, Jiangsu, Changshou City Patentee before: Jiafa Chemical Co., Ltd., Changshu |
|
TR01 | Transfer of patent right |