KR20170104091A - 도로 포장용 에폭시-아스팔트 전처리제 조성물 - Google Patents
도로 포장용 에폭시-아스팔트 전처리제 조성물 Download PDFInfo
- Publication number
- KR20170104091A KR20170104091A KR1020160026522A KR20160026522A KR20170104091A KR 20170104091 A KR20170104091 A KR 20170104091A KR 1020160026522 A KR1020160026522 A KR 1020160026522A KR 20160026522 A KR20160026522 A KR 20160026522A KR 20170104091 A KR20170104091 A KR 20170104091A
- Authority
- KR
- South Korea
- Prior art keywords
- epoxy resin
- asphalt
- ethylene vinyl
- curing agent
- epoxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000010426 asphalt Substances 0.000 title claims abstract description 45
- 239000000203 mixture Substances 0.000 title claims abstract description 45
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 39
- 239000005038 ethylene vinyl acetate Substances 0.000 claims abstract description 24
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical group OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims abstract description 19
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims abstract description 19
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000003822 epoxy resin Substances 0.000 claims description 51
- 229920000647 polyepoxide Polymers 0.000 claims description 51
- 239000003085 diluting agent Substances 0.000 claims description 17
- UXHMSLJUIFRQLH-UHFFFAOYSA-N ethene ethenyl benzoate Chemical compound C=C.C(=C)OC(C1=CC=CC=C1)=O UXHMSLJUIFRQLH-UHFFFAOYSA-N 0.000 claims description 15
- 238000002156 mixing Methods 0.000 claims description 11
- 150000002118 epoxides Chemical class 0.000 claims description 9
- 239000004593 Epoxy Substances 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 125000003277 amino group Chemical group 0.000 claims description 7
- 239000005711 Benzoic acid Substances 0.000 claims description 6
- 235000010233 benzoic acid Nutrition 0.000 claims description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 5
- 229920000768 polyamine Polymers 0.000 claims description 5
- 239000004848 polyfunctional curative Substances 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 4
- 229920002554 vinyl polymer Polymers 0.000 claims description 2
- 239000004841 bisphenol A epoxy resin Substances 0.000 claims 1
- 239000004843 novolac epoxy resin Substances 0.000 claims 1
- 238000003756 stirring Methods 0.000 claims 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical group CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract description 17
- 238000007781 pre-processing Methods 0.000 abstract description 6
- 230000000704 physical effect Effects 0.000 abstract description 5
- 125000003118 aryl group Chemical group 0.000 abstract description 3
- 238000005336 cracking Methods 0.000 abstract description 3
- 239000011230 binding agent Substances 0.000 abstract description 2
- 230000000694 effects Effects 0.000 abstract description 2
- 238000005191 phase separation Methods 0.000 abstract description 2
- 230000002265 prevention Effects 0.000 abstract description 2
- 238000006467 substitution reaction Methods 0.000 abstract description 2
- 238000011109 contamination Methods 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 18
- 150000001412 amines Chemical class 0.000 description 10
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 239000003849 aromatic solvent Substances 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 229920001971 elastomer Polymers 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 238000005452 bending Methods 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000000806 elastomer Substances 0.000 description 4
- 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 4
- 229920003986 novolac Polymers 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000006482 condensation reaction Methods 0.000 description 3
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 239000011259 mixed solution Substances 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 229920005992 thermoplastic resin Polymers 0.000 description 3
- 229920001187 thermosetting polymer Polymers 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- FJLUATLTXUNBOT-UHFFFAOYSA-N 1-Hexadecylamine Chemical compound CCCCCCCCCCCCCCCCN FJLUATLTXUNBOT-UHFFFAOYSA-N 0.000 description 2
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 2
- YSUQLAYJZDEMOT-UHFFFAOYSA-N 2-(butoxymethyl)oxirane Chemical compound CCCCOCC1CO1 YSUQLAYJZDEMOT-UHFFFAOYSA-N 0.000 description 2
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- FACXGONDLDSNOE-UHFFFAOYSA-N buta-1,3-diene;styrene Chemical compound C=CC=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 FACXGONDLDSNOE-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 229920000468 styrene butadiene styrene block copolymer Polymers 0.000 description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 description 1
- JPZYXGPCHFZBHO-UHFFFAOYSA-N 1-aminopentadecane Chemical compound CCCCCCCCCCCCCCCN JPZYXGPCHFZBHO-UHFFFAOYSA-N 0.000 description 1
- LUKZQXIIABXJOH-UHFFFAOYSA-N 2-(2,2-dimethylpropoxymethyl)oxirane Chemical compound CC(C)(C)COCC1CO1 LUKZQXIIABXJOH-UHFFFAOYSA-N 0.000 description 1
- KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 239000009261 D 400 Substances 0.000 description 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- GVKORIDPEBYOFR-UHFFFAOYSA-K [butyl-bis(2-ethylhexanoyloxy)stannyl] 2-ethylhexanoate Chemical compound CCCCC(CC)C(=O)O[Sn](CCCC)(OC(=O)C(CC)CCCC)OC(=O)C(CC)CCCC GVKORIDPEBYOFR-UHFFFAOYSA-K 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- FXXJMLQTXSVBIR-UHFFFAOYSA-N benzoic acid;ethene Chemical compound C=C.OC(=O)C1=CC=CC=C1 FXXJMLQTXSVBIR-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000007809 chemical reaction catalyst Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 150000001923 cyclic compounds Chemical class 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004850 liquid epoxy resins (LERs) Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002730 mercury Chemical class 0.000 description 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 1
- ZWLPBLYKEWSWPD-UHFFFAOYSA-N o-toluic acid Chemical compound CC1=CC=CC=C1C(O)=O ZWLPBLYKEWSWPD-UHFFFAOYSA-N 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- -1 vinyl resin-modified epoxy resins Chemical class 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/24—Macromolecular compounds
- C04B24/28—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C04B24/281—Polyepoxides
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/04—Carboxylic acids; Salts, anhydrides or esters thereof
- C04B24/045—Esters, e.g. lactones
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/24—Macromolecular compounds
- C04B24/26—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Ceramic Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Civil Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
Abstract
과제 해결수단: 본 발명에 따르면, 에폭시-아스팔트 전처리제 조성물 중 상용화제로 사용되던 에틸렌비닐아세테이트의 아세테이트기를 방향족의 벤조에이트기로 치환함에 따라 분자 사슬이 길어지고 극성이 낮아지면서 에폭시-아스팔트 혼합물 간의 상용성이 개선되어 크랙 방지, 유연성 증대, 강도 증가 및 접착력 향상 등 물성 면에서 여러 가지 우수한 개선효과를 보여 주었다.
Description
도 2는 에폭시 수지와 1차 아민의 반응 및 에폭시 수지와 3차 아민의 반응을 나타낸 것이다.
도 3은 본 발명의 일 실시예에 의하여 전처리제 조성물을 혼합하는 두 개의 탱크와 내용물을 예시한 것이다.
도 4는 본 발명의 전처리제 조성물을 현장에서 살포하기 위한 차량의 구조를 예시한 것이다.
| 원료명 | 실시예 1 | 실시예 2 | 비교예 1 | 비교예 2 |
| YD-128 | 23 | - | 23 | - |
| YD-127 | - | 23 | - | 23 |
| PG-207P | 8 | - | 8 | - |
| PGE | - | 8 | - | 8 |
| 헥사데실아민 | 20 | - | 20 | - |
| 시클로헥실아민 | - | 20 | - | 20 |
| AP-5 | 40 | - | 40 | - |
| AP-3 | - | 40 | - | 40 |
| EVA -1540 | - | - | 9 | - |
| EVA -1519 | - | - | - | 9 |
| 합성 1의 결과물(EVB-1) | 9 | - | - | - |
| 합성 2의 결과물(EVB-2) | - | 9 | - | - |
| 합계 | 100 | 100 | 100 | 100 |
| 항목 | 단위 | 실시예 1 | 실시예 2 | 비교예 1 | 비교예 2 | 비고 |
| 혼합물 점도 | cps | 353 | 312 | 501 | 455 | |
| 인장강도 | kg/ cm 2 | 95 | 82 | 73 | 64 | ASTM D638 |
| 신율 | % | 250 | 241 | 130 | 120 | ASTM D638 |
| 접착강도 | kg/ cm 2 | 112 | 92 | 70 | 65 | ASTM D1002 |
|
저온굴곡강도
(15℃) |
kg/ cm 2 | 41 | 35 | 30 | 25 | ASTM D790 |
|
저온충격강도
(15℃) |
kg-cm/ cm 2 | 8.1 | 6.4 | 5.5 | 4.5 | ASTM D256 |
Claims (9)
- 에폭시 수지 40-60중량%, 아스팔트 30-50중량% 및 상용화제로서 에틸렌비닐벤조에이트 5-15중량%를 포함하는 도로 포장용 에폭시-아스팔트 전처리제 조성물.
- 청구항 1에 있어서,
상기 에폭시 수지는 주 에폭시 수지 35-75중량%, 반응성 희석제 10-25중량% 및 경화제 5~45중량%임을 특징으로 하는 도로 포장용 에폭시-아스팔트 전처리제 조성물.
- 청구항 1에 있어서,
상기 에틸렌비닐벤조에이트는 벤조에이트를 31-57중량% 함유한 것임을 특징으로 하는 도로 포장용 에폭시-아스팔트 전처리제 조성물.
- 청구항 1에 있어서,
상기 에틸렌비닐벤조에이트는 에틸렌비닐아세테이트에 벤조산을 질량비 100:40-100:60으로 반응시켜 얻은 것임을 특징으로 하는 도로 포장용 에폭시-아스팔트 전처리제 조성물.
- 청구항 2에 있어서,
상기 주 에폭시 수지는 분자 내에 2개 이상의 반응성 에폭시드를 갖고 있는 당량 150-250의 비스페놀 A형 에폭시 수지 및 페놀 노볼락형 에폭시 수지 중 선택된 1종 이상임을 특징으로 하는 도로 포장용 에폭시-아스팔트 전처리제 조성물.
- 청구항 2에 있어서,
상기 반응성 희석제는 폴리에테르 변성 에폭시 수지, 폴리에스테르 변성 에폭시 수지, 우레탄 변성 에폭시 수지 및 비닐수지 변성 에폭시 수지 중 선택된 1종 이상임을 특징으로 하는 도로 포장용 에폭시-아스팔트 전처리제 조성물.
- 청구항 6에 있어서,
상기 반응성 희석제는 분자량 300-1000의 분자 내에 2개의 반응성 에폭시드를 갖는 폴리에테르 변성 에폭시임을 특징으로 하는 도로 포장용 에폭시-아스팔트 전처리제 조성물.
- 청구항 2에 있어서,
상기 경화제는 분자 내에 탄소를 15-25개 가지며, 반응성 아미노기를 1개 갖고 있는 폴리아민임을 특징으로 하는 도로 포장용 에폭시-아스팔트 전처리제 조성물.
- 가열부재와 고온, 고점도 피디미터를 갖춘 주제 탱크와,
가열부재와 고온, 고점도 피디미터를 갖춘 경화제 탱크와,
상기 주제 탱크 및 상기 경화제 탱크와 연결되어 주제 및 경화제를 혼합하여 교반하는 교반기와,
상기 교반기에서 혼합된 주제와 경화제 혼합물을 가압하는 가압펌프와,
상기 가압된 주제와 경화제 혼합물을 노면에 도포하는 분사기를 포함하는 도로 포장용 에폭시-아스팔트 전처리제 조성물 도포용 차량.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1020160026522A KR101814461B1 (ko) | 2016-03-04 | 2016-03-04 | 도로 포장용 에폭시-아스팔트 전처리제 조성물 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1020160026522A KR101814461B1 (ko) | 2016-03-04 | 2016-03-04 | 도로 포장용 에폭시-아스팔트 전처리제 조성물 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20170104091A true KR20170104091A (ko) | 2017-09-14 |
| KR101814461B1 KR101814461B1 (ko) | 2018-01-05 |
Family
ID=59926776
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020160026522A Active KR101814461B1 (ko) | 2016-03-04 | 2016-03-04 | 도로 포장용 에폭시-아스팔트 전처리제 조성물 |
Country Status (1)
| Country | Link |
|---|---|
| KR (1) | KR101814461B1 (ko) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102047909B1 (ko) * | 2018-12-04 | 2019-11-22 | 주식회사 세일매트릭스 | 가열식 교면방수용 에폭시 아스팔트 바인더 혼합물 및 그 제조방법 |
| KR102180322B1 (ko) * | 2020-07-30 | 2020-11-18 | 주식회사한수나텍 | 반사균열 저감용 고탄성 방수 아스팔트 혼합물 및 이를 이용한 노후 콘크리트 도로 전면 보수방법 |
| CN114539796A (zh) * | 2022-03-07 | 2022-05-27 | 鄂尔多斯市路泰公路工程有限责任公司 | 一种耐高温的路用环氧沥青及其制备方法 |
| CN117050541A (zh) * | 2023-07-27 | 2023-11-14 | 山东百成新材料科技股份有限公司 | 一种公路用耐高温复合改性沥青及其制备方法 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4693440B2 (ja) * | 2005-03-01 | 2011-06-01 | 株式会社近代化成 | 道路舗装用エポキシ樹脂プライマー組成物とそれを用いた道路舗装方法 |
| ATE421490T1 (de) * | 2006-07-24 | 2009-02-15 | Akzo Nobel Nv | Verwendung von polymerpulver in pflasterfugenmörteln |
-
2016
- 2016-03-04 KR KR1020160026522A patent/KR101814461B1/ko active Active
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102047909B1 (ko) * | 2018-12-04 | 2019-11-22 | 주식회사 세일매트릭스 | 가열식 교면방수용 에폭시 아스팔트 바인더 혼합물 및 그 제조방법 |
| KR102180322B1 (ko) * | 2020-07-30 | 2020-11-18 | 주식회사한수나텍 | 반사균열 저감용 고탄성 방수 아스팔트 혼합물 및 이를 이용한 노후 콘크리트 도로 전면 보수방법 |
| CN114539796A (zh) * | 2022-03-07 | 2022-05-27 | 鄂尔多斯市路泰公路工程有限责任公司 | 一种耐高温的路用环氧沥青及其制备方法 |
| CN117050541A (zh) * | 2023-07-27 | 2023-11-14 | 山东百成新材料科技股份有限公司 | 一种公路用耐高温复合改性沥青及其制备方法 |
| CN117050541B (zh) * | 2023-07-27 | 2024-05-28 | 山东百成新材料科技股份有限公司 | 一种公路用耐高温复合改性沥青及其制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| KR101814461B1 (ko) | 2018-01-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| RU2418816C2 (ru) | Эпоксидные смолы, содержащие отверждающий агент на основе циклоалифатического диамина | |
| EP2433985B1 (en) | Improved epoxy systems for composites | |
| EP3074475B1 (en) | Polyurethane based asphalt composition | |
| HK1005034B (en) | Flexibiliser combinations for epoxy resins | |
| KR101814461B1 (ko) | 도로 포장용 에폭시-아스팔트 전처리제 조성물 | |
| HK1005034A1 (en) | Flexibiliser combinations for epoxy resins | |
| WO2006093949A9 (en) | Two-component epoxy adhesive composition | |
| CN101220197A (zh) | 多胺料流作为环氧粘合剂和地板材料中的固化剂的用途 | |
| JPH02232223A (ja) | エポキシ樹脂用の為の硬化剤としてポリアミドアミンを用いる方法および該ポリアミドアミンを含有する硬化性混合物 | |
| WO2017049578A1 (en) | Epoxy resin composition | |
| US20230332025A1 (en) | Two-part epoxy-based structural adhesive composition | |
| US3755226A (en) | Epoxy bitumen system for road surfacing | |
| US3363026A (en) | Epoxy resin containing a curing catalyst mixture of a polymercaptan and a fused ringamine | |
| GB2061951A (en) | Epoxy curing system | |
| KR102425139B1 (ko) | 우레탄 함유 에폭시 수지, 이를 포함하는 에폭시 수지 조성물 및 이를 포함하는 에폭시 접착제 조성물 | |
| JPS5984916A (ja) | 硬化剤としてポリオキシアルキレンジアミンビグアナイド塩を有するエポキシ樹脂組成物 | |
| KR101858015B1 (ko) | 접착력이 향상된 알파메틸 스티렌네이티드 알킬페놀 및 이를 함유하는 조성물 | |
| JP5398541B2 (ja) | ヒドロキシエステルで予備鎖延長したエポキシ末端増粘剤およびその製造方法 | |
| KR20140002990A (ko) | 접착력이 향상된 스티렌네이티드 알킬페놀 및 이를 함유하는 조성물 | |
| EP4015557A1 (en) | Two component (2k) epoxy formulation | |
| JP3661358B2 (ja) | 液状エポキシ樹脂組成物およびコンクリート構造物の補修・補強方法 | |
| US20220282137A1 (en) | Fast curing oil tolerant adhesive compositions | |
| JP2005113103A (ja) | エポキシ塗料組成物 | |
| ES2973297T3 (es) | Composiciones epoxi catiónicas | |
| KR102602066B1 (ko) | 비스페놀-z 폴리우레탄을 포함하는 이액형 접착제 조성물 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A201 | Request for examination | ||
| PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 20160304 |
|
| PA0201 | Request for examination | ||
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20161220 Patent event code: PE09021S01D |
|
| PG1501 | Laying open of application | ||
| E701 | Decision to grant or registration of patent right | ||
| PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 20170926 |
|
| GRNT | Written decision to grant | ||
| PR0701 | Registration of establishment |
Comment text: Registration of Establishment Patent event date: 20171227 Patent event code: PR07011E01D |
|
| PR1002 | Payment of registration fee |
Payment date: 20171227 End annual number: 3 Start annual number: 1 |
|
| PG1601 | Publication of registration | ||
| PR1001 | Payment of annual fee |
Payment date: 20201124 Start annual number: 4 End annual number: 4 |
|
| PR1001 | Payment of annual fee |
Payment date: 20211206 Start annual number: 5 End annual number: 5 |
|
| PR1001 | Payment of annual fee |
Payment date: 20221021 Start annual number: 6 End annual number: 6 |
|
| PR1001 | Payment of annual fee |
Payment date: 20231130 Start annual number: 7 End annual number: 7 |
|
| PR1001 | Payment of annual fee |
Payment date: 20241218 Start annual number: 8 End annual number: 8 |