KR100629902B1 - Epoxy Resin Composition for Asphalt Pavement and Epoxy Asphalt Pavement Mixture Using the Same - Google Patents
Epoxy Resin Composition for Asphalt Pavement and Epoxy Asphalt Pavement Mixture Using the Same Download PDFInfo
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- KR100629902B1 KR100629902B1 KR1020060063304A KR20060063304A KR100629902B1 KR 100629902 B1 KR100629902 B1 KR 100629902B1 KR 1020060063304 A KR1020060063304 A KR 1020060063304A KR 20060063304 A KR20060063304 A KR 20060063304A KR 100629902 B1 KR100629902 B1 KR 100629902B1
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- 239000000203 mixture Substances 0.000 title claims abstract description 84
- 239000010426 asphalt Substances 0.000 title claims abstract description 80
- 239000004593 Epoxy Substances 0.000 title claims abstract description 51
- 239000003822 epoxy resin Substances 0.000 title claims abstract description 45
- 229920000647 polyepoxide Polymers 0.000 title claims abstract description 45
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 12
- 229920000768 polyamine Polymers 0.000 claims abstract description 12
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 10
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims abstract description 8
- 150000002118 epoxides Chemical group 0.000 claims abstract description 8
- 229920003986 novolac Polymers 0.000 claims abstract description 5
- 150000001412 amines Chemical class 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 239000011342 resin composition Substances 0.000 claims description 6
- 239000002344 surface layer Substances 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 2
- 238000006482 condensation reaction Methods 0.000 claims description 2
- 238000005056 compaction Methods 0.000 claims 6
- WAMBUHSSUGGLJO-UHFFFAOYSA-N 4-[2-(4-hydroxyphenyl)propan-2-yl]phenol;2-(oxiran-2-ylmethoxymethyl)oxirane Chemical compound C1OC1COCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 WAMBUHSSUGGLJO-UHFFFAOYSA-N 0.000 claims 1
- 230000018044 dehydration Effects 0.000 claims 1
- 238000006297 dehydration reaction Methods 0.000 claims 1
- 229910052709 silver Inorganic materials 0.000 claims 1
- 239000004332 silver Substances 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 230000000704 physical effect Effects 0.000 abstract description 10
- 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 abstract description 8
- 229940106691 bisphenol a Drugs 0.000 abstract description 4
- 238000004806 packaging method and process Methods 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 239000007788 liquid Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 239000004848 polyfunctional curative Substances 0.000 description 3
- 230000008439 repair process Effects 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000006735 epoxidation reaction Methods 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- OWMNWOXJAXJCJI-UHFFFAOYSA-N 2-(oxiran-2-ylmethoxymethyl)oxirane;phenol Chemical compound OC1=CC=CC=C1.OC1=CC=CC=C1.C1OC1COCC1CO1 OWMNWOXJAXJCJI-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 206010039203 Road traffic accident Diseases 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000011384 asphalt concrete Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 239000004841 bisphenol A epoxy resin Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000004567 concrete Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000945 filler Substances 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
- 239000003112 inhibitor Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- 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
- 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
- C04B16/00—Use of organic materials as fillers, e.g. pigments, for mortars, concrete or artificial stone; Treatment of organic materials specially adapted to enhance their filling properties in mortars, concrete or artificial stone
- C04B16/04—Macromolecular compounds
-
- 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
- C08G59/20—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 characterised by the epoxy compounds used
- C08G59/22—Di-epoxy compounds
- C08G59/226—Mixtures of di-epoxy compounds
-
- 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
- C08G59/40—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 characterised by the curing agents used
- C08G59/50—Amines
- C08G59/5006—Amines aliphatic
- C08G59/5013—Amines aliphatic containing more than seven carbon atoms, e.g. fatty amines
-
- 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
- C08G59/40—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 characterised by the curing agents used
- C08G59/50—Amines
- C08G59/56—Amines together with other curing agents
-
- 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
- C08G59/40—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 characterised by the curing agents used
- C08G59/62—Alcohols or phenols
- C08G59/621—Phenols
-
- 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
- C08L63/04—Epoxynovolacs
-
- 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
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- E—FIXED CONSTRUCTIONS
- E01—CONSTRUCTION OF ROADS, RAILWAYS, OR BRIDGES
- E01C—CONSTRUCTION OF, OR SURFACES FOR, ROADS, SPORTS GROUNDS, OR THE LIKE; MACHINES OR AUXILIARY TOOLS FOR CONSTRUCTION OR REPAIR
- E01C11/00—Details of pavings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Structural Engineering (AREA)
- Materials Engineering (AREA)
- Civil Engineering (AREA)
- Ceramic Engineering (AREA)
- Architecture (AREA)
- Road Paving Structures (AREA)
- Epoxy Resins (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
본 발명은 내유동성, 균열저항성 등이 향상된 아스팔트용 에폭시 수지 조성물 및 이를 이용한 에폭시 아스팔트 조성물에 관한 것으로서, 좀더 구체적으로는 분자량 300~1,500이고, 분자구조 내 에폭사이드기가 2개 이상인 디글리시딜 에테르(Diglycidyl Ether) 비스페놀-A형 에폭시 수지, 분자량 500~2,000이고, 분자구조 내 에폭사이드기가 2.2개 이상인 페놀 노볼락 폴리글리시딜 에테르(Phenol Novolac Polyglycidyl Ether) 에폭시 수지 등을 주제로 하고 폴리아민을 경화제로 하는 에폭시 수지 조성물에 관한 것으로서, 물성이 개선된 에폭시 수지 조성물을 제공한다.The present invention relates to an epoxy resin composition for asphalt with improved flow resistance, crack resistance, and the like, an epoxy asphalt composition using the same, more specifically, a diglycidyl ether having a molecular weight of 300 to 1,500 and two or more epoxide groups in a molecular structure. (Diglycidyl Ether) Bisphenol-A type epoxy resin, molecular weight 500-2,000, the phenolic novolac polyglycidyl ether epoxy resin having 2.2 or more epoxide groups in the molecular structure and the like, polyamine curing agent The present invention relates to an epoxy resin composition comprising an epoxy resin composition having improved physical properties.
에폭시 수지, 아스팔트, 내구성 Epoxy resin, asphalt, durable
Description
본 발명은 내유동성, 균열저항성 등이 향상된 아스팔트용 에폭시 수지 조성물 및 이를 이용한 에폭시 아스팔트 조성물에 관한 것으로서, 좀더 구체적으로는 분자량 300~1,500이고, 분자구조 내 에폭사이드기가 2개 이상인 디글리시딜 에테르(Diglycidyl Ether) 비스페놀-A형 에폭시 수지, 분자량 500~2,000이고, 분자구조 내 에폭사이드기가 2.2개 이상인 페놀 노볼락 폴리글리시딜 에테르(Phenol Novolac Polyglycidyl Ether) 에폭시 수지 등을 주제로 하고 폴리아민을 경화제로 하는 에폭시 수지 조성물에 관한 것으로서, 마샬안정도, 동적안정도 등의 물성이 현저히 개선된 에폭시 수지 조성물을 제공한다.The present invention relates to an epoxy resin composition for asphalt with improved flow resistance, crack resistance, and the like, an epoxy asphalt composition using the same, more specifically, a diglycidyl ether having a molecular weight of 300 to 1,500 and two or more epoxide groups in a molecular structure. (Diglycidyl Ether) Bisphenol-A type epoxy resin, molecular weight 500-2,000, the phenolic novolac polyglycidyl ether epoxy resin having 2.2 or more epoxide groups in the molecular structure and the like, polyamine curing agent The present invention relates to an epoxy resin composition comprising a epoxy resin composition with remarkably improved physical properties such as Marshall stability and dynamic stability.
교통량의 증대, 차량의 대형화 등 도로포장의 교통조건은 매년 악화하고 있다. 이와 같은 중교통 도로에서는 소성변형의 발생이 현저하게 되고 있으며, 보수공사 사이클이 매년 짧아지고 있다. 그리하여 보수 공사가 증대되고 있고, 도로 이 용자들은 공사 지체에 의한 시간 손실 문제, 도로 주변의 주민들은 보수 공사로 인한 소음 및 진동 등으로 주거환경이 악화하는 문제, 시공업자들은 교통 규제 인원과 비용 등이 소요되는 등 많은 문제가 발생하고 있어서, 이와 같은 상황에서 좀더 내구성이 있는 포장이 요구되고 있다. 본 발명의 아스팔트 에폭시 수지 조성물은 아스팔트와 가소성 에폭시 수지를 이용한 가열 아스팔트 혼합물로 매우 높은 내유동 성능이 얻어진다.Traffic conditions for road pavement, such as increased traffic volume and larger vehicles, are deteriorating every year. The occurrence of plastic deformation is remarkable on such heavy traffic roads, and the repair cycle is getting shorter every year. As a result, repair work is increasing, road users suffer from time loss due to construction delays, residents around the road deteriorate the living environment due to noise and vibration, etc. Many problems have arisen such as this, and in such a situation, more durable packaging is calculated | required. Asphalt epoxy resin composition of the present invention is very high flow resistance performance is obtained with a heated asphalt mixture using asphalt and plastic epoxy resin.
한편, 최근의 교량은 장대화하는 경향이 있으며, 콘크리트 상판을 대신하여 강상판이 증가하고 있다. 그러나 이러한 강상판 포장에서는 종단균열이나 소성변형이 발생하여 큰 문제로 되고 있다. 그 중에서도 에폭시 아스팔트 조성물로 포장한 강상판 포장은 20년 이상의 공용에서도 내구적으로 양호한 노면 성상을 나타낸다고 알려져 있다.On the other hand, the recent bridges tend to be long, and steel plates are increasing in place of concrete decks. However, in such steel sheet packaging, longitudinal cracking and plastic deformation occur, which is a serious problem. Among them, the steel sheet pavement packaged with the epoxy asphalt composition is known to exhibit durable road surface characteristics even in public for over 20 years.
아스팔트에 에폭시 수지를 부가한 에폭시 아스팔트 조성물을 이용한 도로 포장은 포장 수명이 증대되었으며, 수명 증대와 함께 이를 가능한 한 양호하게 유지하려는 시도가 계속되고 있다.Road pavement using an epoxy asphalt composition in which epoxy resin is added to asphalt has increased pavement life, and attempts to keep it as good as possible with increasing life span continue.
그러나, 지금까지 개발된 여러 가지 에폭시 아스팔트 조성물은 균열저항성이나 시공성 등에서 여전히 개선의 여지가 있었고, 또한 혼합되는 골재 입경 등의 조건에 따라 물성이 좌우되는 문제점이 있었다.However, various epoxy asphalt compositions developed so far still have room for improvement in crack resistance and workability, and also have problems in which physical properties depend on conditions such as aggregate particle size to be mixed.
따라서, 본 발명은 상기 에폭시 아스팔트 조성물 및 포장재에 따른 문제점을 해결하고 마샬안정도, 동적안정도 등이 개선된 아스팔트용 에폭시 조성물과 이를 이용한 에폭시 아스팔트 조성물을 제공함에 그 목적이 있다.Accordingly, an object of the present invention is to solve the problems caused by the epoxy asphalt composition and pavement, and to provide an epoxy composition for asphalt and an epoxy asphalt composition using the same having improved Marshall stability and dynamic stability.
상기 목적을 달성하기 위하여 본 발명자는 아스팔트용 에폭시 수지 조성물을 연구한 결과 마샬안정도, 동적안정도 등이 향상된 아스팔트용 에폭시 수지 조성물을 발명하기에 이르렀다.In order to achieve the above object, the present inventors have studied the epoxy resin composition for asphalt, and thus, invented the epoxy resin composition for asphalt with improved Marshall stability and dynamic stability.
본 명세서에서 "에폭시 수지 조성물"은 에폭시 주제와 경화제를 혼합한 상태의 조성물을 의미하며, "에폭시 아스팔트 조성물"은 본 발명의 아스팔트용 에폭시 수지와 일반 아스팔트(일명 스트레이트 아스팔트)를 혼합한 상태의 조성물을 말하며, "에폭시 아스팔트 포장 혼합물"은 상기 에폭시 아스팔트 조성물에 골재를 혼합하여 도로에 포장할 수 있는 상태의 혼합물을 말하는 것이다.As used herein, the term "epoxy resin composition" refers to a composition of a mixture of an epoxy main material and a curing agent, and "epoxy asphalt composition" refers to a composition of a mixture of an epoxy resin for asphalt of the present invention and general asphalt (aka straight asphalt). "Epoxy asphalt pavement mixture" refers to a mixture that can be paved on the road by mixing aggregate with the epoxy asphalt composition.
본 발명의 에폭시 수지 주제는 비스페놀(Bisphenol)-A와 에피클로로히드린(Epichlorohydrine)과 에폭시화 반응에 의하여 생성된 분자량 300~1,500이고, 분자구조 내 에폭사이드기가 2개 이상인 디글리시딜 에테르(Diglycidyl Ether) 비스페놀-A형 에폭시 수지(하기 화학식 1), 페놀 노볼락 수지(Phenol Novolac resin)와 에피클로로히드린과의 에폭시화 반응에 의하여 생성된 분자량 500~2,000이고 분자구조 내 에폭사이드기가 2.2개 이상인 페놀 노볼락 폴리글리시딜 에테르(Phenol Novolac Polyglycidyl Ether) 에폭시 수지(하기 화학식 2), 또는 화학식 1과 화학식 2로 표시되는 화합물의 혼합물 및 화학식 1, 화학식 2, 화학식 1과 2의 혼합물에 화학식 3, 4, 5로 표시되는 모노글리시딜 에테르 또는 폴리글리시딜 에테르 에폭시 수지가 1종 이상 부가된 에폭시 수지를 포함한다.The main subject of the epoxy resin of the present invention is 300-1,500 molecular weight produced by epoxidation reaction with Bisphenol-A and Epichlorohydrine, and diglycidyl ether having two or more epoxide groups in the molecular structure ( Diglycidyl Ether) Bisphenol-A type epoxy resin (Formula 1), phenol novolac resin and epoxidation reaction of epichlorohydrin with a molecular weight of 500 ~ 2,000 produced by the epoxide group 2.2 At least one phenol novolac polyglycidyl ether epoxy resin (Formula 2), or a mixture of compounds represented by formulas 1 and 2 and mixtures of formulas 1, 2, 1 and 2 An epoxy resin to which at least one monoglycidyl ether or polyglycidyl ether epoxy resin represented by the formulas (3), (4) and (5) is added.
(단, 상기 식에서 n=1~5이다.)(Wherein n = 1 to 5)
(단, 상기 식에서 n=1~5이다.)(Wherein n = 1 to 5)
또한, 상기 에폭시 주제에는 포장재의 균열 방지와 휨 강도 증가를 목적으로 염화고무 등 공지의 강화제를 주제의 물성에 큰 영향을 미치지 않는 범위 내에서 부가할 수 있다. 그 밖에도 착색제(안료), 침강방지제 등 공지의 첨가제를 주제의 물성에 큰 영향을 미치지 않는 범위 내에서 부가할 수 있다.In addition, a known reinforcing agent such as rubber chloride may be added to the epoxy base material within the range of not significantly affecting the base material properties for the purpose of preventing cracking of the packaging material and increasing bending strength. In addition, well-known additives, such as a coloring agent (pigment) and a sedimentation inhibitor, can be added within the range which does not largely affect the physical property of a subject.
에폭시 수지의 경화제로는 아민, 폴리아민, 페놀 또는 아민, 폴리아민과 페놀을 탈수 축합 반응시켜 얻어지는 조성물을 사용한다. 폴리아민은 지방족 폴리아민, 방향족 폴리아민, 지환족 폴리아민 및 이들 분자의 말단에 적어도 한 개의 제1급 아민기를 가진 폴리아미드류로 변성시킨 것을 포함하며, 바람직하게는 지방족 폴리아민을 사용한다.As a hardening | curing agent of an epoxy resin, the composition obtained by dehydrating condensation reaction of an amine, a polyamine, a phenol or an amine, a polyamine, and a phenol is used. Polyamines include those modified with aliphatic polyamines, aromatic polyamines, cycloaliphatic polyamines and polyamides having at least one primary amine group at the ends of these molecules, preferably aliphatic polyamines.
위에서 개시한 1종 이상의 에폭시 수지에 저온에서 경화를 가속화시킬 수 있는 경화촉매를 첨가하여 주제 조성물을 제조하고, 상기 경화제 조성물을 제조하여, 주제와 경화제를 중량 대비 1~5:1 비율로 혼합하고, 바람직하게는 주제:경화제=10:7의 비율로 혼합하여 본 발명의 아스팔트용 에폭시 수지 조성물을 얻을 수 있다.The main composition is prepared by adding a curing catalyst capable of accelerating curing at low temperature to one or more epoxy resins disclosed above, and preparing the curing agent composition to mix the main body and the curing agent in a ratio of 1 to 5: 1 by weight. Preferably, the epoxy resin composition for asphalt of the present invention can be obtained by mixing in a ratio of subject: hardener = 10: 7.
또한, 본 발명의 아스팔트용 에폭시 수지 조성물은 에폭시 아스팔트 조성물 100중량% 중 10~50중량%가 바람직하다. 10중량% 미만인 경우 에폭시 수지에 의한 물성 향상 효과가 거의 나타나지 아니하며, 50중량%를 초과하는 경우 경제적이지 못하다.Moreover, as for the epoxy resin composition for asphalt of this invention, 10-50 weight% is preferable in 100 weight% of epoxy asphalt compositions. If the content is less than 10% by weight, the physical property improvement effect by the epoxy resin is hardly exhibited, and when it is more than 50% by weight, it is not economical.
또한, 본 발명에서 상기 에폭시 아스팔트 수지 조성물에 골재를 혼합한 에폭시 아스팔트 포장 혼합물에는 혼합물 전체 중량 100%를 기준으로 에폭시 아스팔트 수지 조성물이 0.1~10중량% 혼합될 수 있다. 에폭시 아스팔트 수지 조성물이 0.1중량% 미만인 경우, 에폭시 수지에 의한 물성 향상 효과가 거의 나타나지 아니하며, 10중량%를 초과하는 경우 경제적이지 못하다.In addition, in the present invention, the epoxy asphalt pavement mixture in which the aggregate is mixed with the epoxy asphalt resin composition may be 0.1 to 10% by weight of the epoxy asphalt resin composition based on 100% of the total weight of the mixture. When the epoxy asphalt resin composition is less than 0.1% by weight, there is little effect of improving the physical properties by the epoxy resin, and when it exceeds 10% by weight, it is not economical.
또한, 상기 골재로서는 재생골재를 전부 또는 일부 사용할 수 있다.In addition, all or part of recycled aggregate may be used as the aggregate.
본 발명의 에폭시 아스팔트 포장 혼합물의 기층면 포장 방법의 일례를 설명한다. 아스콘 플랜트에서 165±10℃ 온도조건으로 에폭시 아스팔트 포장 혼합물을 제조하고, 현장으로 덤프 트럭 등을 이용하여 운반한 다음, 아스팔트 피니셔로 포설한 후, 1차 전압(다짐)은 130±10℃에서 8~10ton 타이어 롤러로 3회 왕복, 2차 전압은 90±10℃에서 10~12ton 타이어 롤러로 3회 왕복, 3차 전압은 70±10℃에서 8~10ton 타이어 롤러로 3회 왕복하여 기층면을 포장한다.An example of the base surface pavement method of the epoxy asphalt pavement mixture of this invention is demonstrated. Asphalt plant prepared epoxy asphalt pavement mixture at 165 ± 10 ℃, transported to site by dump truck, installed in asphalt finisher, and the primary voltage (compact) was 8 at 130 ± 10 ℃. 3 times reciprocating with ~ 10ton tire roller, 2nd voltage reciprocating 3 times with 10 ~ 12ton tire roller at 90 ± 10 ℃, 3rd voltage reciprocating 3 times with 8 ~ 10ton tire roller at 70 ± 10 ℃ Pack it.
이와 같이 포장된 기층면 위에 에폭시 아스팔트 포장 혼합물을 아스콘 플랜트에서 160±10℃의 고온에서 생산하여 덤프 트럭으로 운반하여 아스팔트 피니셔로 포설한 다음 1차 전압은 130±10℃에서 10~12ton 마카뎀 롤러 3회 왕복, 2차 전압은 90±10℃에서 8~10ton 타이어 롤러로 3회 왕복, 3차 전압은 70±10℃에서 7~8ton 탄뎀 롤러로 3회 왕복하여 표층면을 포장한다.Epoxy asphalt pavement mixture was produced on asphalt pavement at high temperature of 160 ± 10 ℃ in asphalt plant and transported by dump truck and installed in asphalt finisher.The primary voltage was 10 ~ 12ton Macadamel roller at 130 ± 10 ℃. 3 round trips, secondary voltage is 3 round trips with 8-10ton tire roller at 90 ± 10 ℃ and 3rd round trips with 7-8ton tandem roller at 70 ± 10 ℃ to wrap surface layer.
본 발명의 에폭시 아스팔트 포장 혼합물은 기층면 포장재로 사용될 수 있으며, 표층면 포장재로 사용될 수도 있다. 기층면과 표층면을 모두 본 발명의 에폭시 아스팔트 포장 혼합물을 사용하여 포장할 수도 있다. 또한, 본 발명의 에폭시 아스팔트 포장 혼합물이 아닌 다른 포장 혼합물로 기층을 포장하고, 본 발명의 에폭시 아스팔트 포장 혼합물을 표층에 포장할 수 있으며, 그 반대 또한 가능하다.The epoxy asphalt pavement mixture of the present invention can be used as a base pavement and can also be used as a surface pavement. Both the base and surface layers may be paved using the epoxy asphalt pavement mixture of the present invention. It is also possible to wrap the base layer with a pavement mixture other than the epoxy asphalt pavement mixture of the present invention, and to package the epoxy asphalt pavement mixture of the present invention on the surface layer and vice versa.
상기 포장 방법은 여러 방법 중 일례를 예시한 것으로 그 기재에만 한정되는 것이 아님은 본 발명이 속하는 기술분야에서 통상의 지식을 가진 자에게 자명하다.It is apparent to those skilled in the art that the packaging method exemplifies one of several methods and is not limited only to the description thereof.
종래의 에폭시 아스팔트 조성물은 높은 온도에서 경화가 지나치게 빨리 일어남으로 인하여 작업성이 현저히 저하되는 문제점이 있었다. 그러나, 본 발명의 아스팔트용 에폭시 수지는 고온에서 경화 속도를 늦춤으로써 물성과 함께 작업성이 향상되는 결과를 얻을 수 있는 것이다.Conventional epoxy asphalt composition has a problem that the workability is significantly lowered because the curing occurs too fast at high temperatures. However, the epoxy resin for asphalt according to the present invention can obtain a result of improving workability along with physical properties by slowing down the curing speed at a high temperature.
상기 에폭시 수지 주제와 경화제의 물성을 아래 표 1, 표 2, 표 3에 나타내 었다. 또한, 표 4, 표 5는 본 발명의 에폭시 아스팔트 조성물의 물성을 나타내었다. 이때 에폭시 아스팔트 조성물 중 에폭시 수지는 35%이고, 에폭시 수지 중 주제: 경화제=10:7이다.Physical properties of the epoxy resin main material and the curing agent are shown in Table 1, Table 2, and Table 3 below. In addition, Table 4, Table 5 shows the physical properties of the epoxy asphalt composition of the present invention. At this time, the epoxy resin in the epoxy asphalt composition is 35%, the main ingredient in the epoxy resin: curing agent = 10: 7.
다음의 실시예 및 비교예는 본 발명을 좀 더 구체적으로 설명하려는 것으로서, 본 발명의 범위가 실시예의 기재에만 한정되는 것은 아니다.The following examples and comparative examples are intended to illustrate the present invention in more detail, and the scope of the present invention is not limited only to the description of the examples.
[실시예 1]Example 1
에폭시 당량 190(g/eq), 점도 12,400cps(25℃), 무색 투명액체인 디글리시딜 에테르 비스페놀 A형 에폭시 수지 100중량%에 경화촉매로서 페놀 7.6 중량%를 혼합기에 넣고 1,000rpm 속도의 교반기로 30분간 혼합하여 완전히 혼합하여 주제 조성물을 제조하였다.Epoxy equivalent 190 (g / eq), viscosity 12,400cps (25 ℃), colorless transparent liquid, 100% by weight of diglycidyl ether bisphenol A epoxy resin, 7.6% by weight of phenol as a curing catalyst was added to the mixer at a speed of 1,000 rpm. The subject composition was prepared by mixing for 30 minutes with a stirrer and thoroughly mixing.
경화제는 아민가 함량 250MgKOH/g, 점도 39cps(25℃), 비중 0.827의 액체 지방족 폴리아민을 준비하였다.The curing agent prepared a liquid aliphatic polyamine having an amine number content of 250 MgKOH / g, a viscosity of 39 cps (25 ° C), and a specific gravity of 0.827.
상기 주제 조성물과 상기 경화제 조성물을 중량 대비 10:7의 비율로 교반기로 신속하게 혼합하여 본 발명의 아스팔트용 에폭시 수지 조성물을 제조하였다.The epoxy composition for asphalt of the present invention was prepared by rapidly mixing the main composition and the curing agent composition with a stirrer at a ratio of 10: 7 by weight.
[실시예 2]Example 2
상기 실시예 1의 아스팔트용 에폭시 수지 조성물에 일반 아스팔트와 골재를 혼합하여 에폭시 아스팔트 포장 혼합물을 제조하였다. 상기 실시예 1에서 제조한 아스팔트용 에폭시 수지 조성물을 각각 25중량%, 30중량%, 35중량%, 잔량의 아스팔트를 혼합하여 에폭시 아스팔트 조성물을 제조하였다.General asphalt and aggregate were mixed with the epoxy resin composition for asphalt of Example 1 to prepare an epoxy asphalt pavement mixture. An epoxy asphalt composition was prepared by mixing 25% by weight, 30% by weight, 35% by weight, and the remaining amount of asphalt, respectively, in the epoxy resin composition for asphalt prepared in Example 1.
13mm 이하 골재{표 6; 골재 표준입도(통과 백분율: %)}를 93.3중량%, 상기 에폭시 아스팔트 조성물 6.7중량%를 165℃에서 가열, 혼합하여 본 발명의 에폭시 아스팔트 포장 혼합물을 제조하였다.Aggregates up to 13 mm {Table 6; Aggregate standard particle size (% of passage)} was 93.3% by weight, and 6.7% by weight of the epoxy asphalt composition was heated and mixed at 165 ° C. to prepare an epoxy asphalt pavement mixture of the present invention.
[비교예 1]Comparative Example 1
하기 표 7과 같은 입도의 13mm 이하 골재 94.3중량%와 아스팔트 5.7중량%를 혼합하여 본 발명이 속하는 기술분야에서 통상의 지식을 가진 자들에게 "#78"로 호칭되는 아스팔트 포장 혼합물을 제조하였다.94.3% by weight of aggregates of 13 mm or less in aggregate and 5.7% by weight of an aggregate having a particle size as shown in Table 7 below, to prepare an asphalt pavement mixture called "# 78" to those skilled in the art.
[비교예 2]Comparative Example 2
개질제 8중량%(아스팔트 100중량% 기준)를 포함하는 아스팔트 5.7중량%에 상기 표 7과 같은 입도의 13mm 이하 골재 94.3중량%를 혼합하여 개질 아스콘 포장 혼합물을 제조하였다.Modified asphalt concrete mixture was prepared by mixing 94.3% by weight of 13 mm or less aggregate having a particle size as shown in Table 7 with 5.7% by weight of asphalt containing 8% by weight of modifier (based on 100% by weight of asphalt).
[비교예 3]Comparative Example 3
13mm 단입도 골재 82중량%. 모래 9중량%, 충전재 5중량%, 개질제 12중량%(아스팔트 100중량5 기준)를 포함하는 아스팔트 5중량%를 혼합하여 배수성 아스콘 포장 혼합물을 제조하였다.82mm by 13mm single grain aggregate. A drainage ascon pavement mixture was prepared by mixing 5% by weight asphalt, including 9% by weight sand, 5% filler and 12% by weight modifier (based on 100% asphalt 5).
[에폭시 수지 함량에 따른 변화][Changes According to Epoxy Resin Content]
위 실시예 2에서 제조된 에폭시 아스팔트 포장 혼합물(에폭시 아스팔트 조성물 중 에폭시 농도 각각 25중량%, 30중량%, 35중량%)에 대하여 마샬안정도, 동적안정도, 공극률을 각각 KSF2337:2002, KSF2374:2000, KSF2349:2004에 규정된 방법으로 측정하였다. 측정 결과를 표 8에 나타내었다.Marshall stability, dynamic stability, and porosity of the epoxy asphalt pavement mixture (25 wt%, 30 wt%, 35 wt% of the epoxy concentration in the epoxy asphalt composition, respectively) prepared in Example 2 were respectively KSF2337: 2002, KSF2374: 2000, It measured by the method of KSF2349: 2004. The measurement results are shown in Table 8.
[본 발명의 포장 혼합물과 타 포장 혼합물 비교][Comparison of Packaging Mixtures and Other Packaging Mixtures of the Present Invention]
상기 실시예 2(에폭시 수지 조성물 함량 35중량%)및 비교예 1 내지 3의 포장 혼합물에 대하여 각각 KSF2337:2002, KSF2374:2000, KSF2349:2004에 규정한 방법으로 마샬안정도 및 동적안정도, 공극률을 측정하였다. 결과를 표 9에 나타내었다.Marshall stability, dynamic stability, and porosity of the packaging mixtures of Example 2 (the epoxy resin composition content of 35 wt%) and Comparative Examples 1 to 3 were measured by the methods specified in KSF2337: 2002, KSF2374: 2000, and KSF2349: 2004, respectively. It was. The results are shown in Table 9.
본 발명의 에폭시 수지 조성물 및 이를 이용한 에폭시 아스팔트 포장 혼합물은 마샬안정도, 동적안정도 등의 물성이 현저히 개선된 것으로 나타나 잦은 도로 보수에 따른 복잡한 도시교통 장해를 해소하고, 도로의 결함으로 인한 교통사고 발생을 예방할 수 있으며, 국가재정낭비를 줄일 수 있다.The epoxy resin composition of the present invention and the epoxy asphalt pavement mixture using the same have significantly improved physical properties such as Marshall stability and dynamic stability, thereby eliminating complicated urban traffic obstacles caused by frequent road repairs, and preventing traffic accidents caused by road defects. It can prevent and reduce national fiscal waste.
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KR100994195B1 (en) | 2008-05-10 | 2010-11-12 | 주식회사 홍서이엔씨 | Epoxy composition for asphalt pavement, asphalt pavement composition, bridge pavement repair and road repair |
KR101028337B1 (en) * | 2010-07-23 | 2011-04-11 | 박정호 | High durability heated epoxy resin packaging material mixture and construction method |
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