JPH01278482A - Lining of acrylic resin - Google Patents
Lining of acrylic resinInfo
- Publication number
- JPH01278482A JPH01278482A JP10567288A JP10567288A JPH01278482A JP H01278482 A JPH01278482 A JP H01278482A JP 10567288 A JP10567288 A JP 10567288A JP 10567288 A JP10567288 A JP 10567288A JP H01278482 A JPH01278482 A JP H01278482A
- Authority
- JP
- Japan
- Prior art keywords
- monomer
- solutions
- solution
- meth
- lining
- 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
- 239000004925 Acrylic resin Substances 0.000 title claims description 10
- 229920000178 Acrylic resin Polymers 0.000 title claims description 10
- 239000000178 monomer Substances 0.000 claims abstract description 21
- 239000011347 resin Substances 0.000 claims abstract description 13
- 229920005989 resin Polymers 0.000 claims abstract description 13
- 229920000642 polymer Polymers 0.000 claims abstract description 10
- 238000002156 mixing Methods 0.000 claims abstract description 9
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims abstract description 8
- 150000002148 esters Chemical class 0.000 claims abstract description 5
- 239000007788 liquid Substances 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 238000006116 polymerization reaction Methods 0.000 claims 1
- 239000003505 polymerization initiator Substances 0.000 abstract description 11
- 239000004014 plasticizer Substances 0.000 abstract description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract description 4
- 150000001875 compounds Chemical class 0.000 abstract description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 12
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 4
- 239000012933 diacyl peroxide Substances 0.000 description 4
- 239000001294 propane Substances 0.000 description 4
- -1 Alkyl peroxide Chemical class 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000012188 paraffin wax Substances 0.000 description 3
- 150000003512 tertiary amines Chemical class 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
- ZTKDMNHEQMILPE-UHFFFAOYSA-N 4-methoxy-n,n-dimethylaniline Chemical compound COC1=CC=C(N(C)C)C=C1 ZTKDMNHEQMILPE-UHFFFAOYSA-N 0.000 description 2
- SJDILFZCXQHCRB-UHFFFAOYSA-N 4-tert-butyl-n,n-dimethylaniline Chemical compound CN(C)C1=CC=C(C(C)(C)C)C=C1 SJDILFZCXQHCRB-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- ZQMIGQNCOMNODD-UHFFFAOYSA-N diacetyl peroxide Chemical compound CC(=O)OOC(C)=O ZQMIGQNCOMNODD-UHFFFAOYSA-N 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- TVWTZAGVNBPXHU-FOCLMDBBSA-N dioctyl (e)-but-2-enedioate Chemical compound CCCCCCCCOC(=O)\C=C\C(=O)OCCCCCCCC TVWTZAGVNBPXHU-FOCLMDBBSA-N 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 230000003670 easy-to-clean Effects 0.000 description 2
- 239000003517 fume Substances 0.000 description 2
- GYVGXEWAOAAJEU-UHFFFAOYSA-N n,n,4-trimethylaniline Chemical compound CN(C)C1=CC=C(C)C=C1 GYVGXEWAOAAJEU-UHFFFAOYSA-N 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 150000004992 toluidines Chemical class 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- CDULGHZNHURECF-UHFFFAOYSA-N 2,3-dimethylaniline 2,4-dimethylaniline 2,5-dimethylaniline 2,6-dimethylaniline 3,4-dimethylaniline 3,5-dimethylaniline Chemical group CC1=CC=C(N)C(C)=C1.CC1=CC=C(C)C(N)=C1.CC1=CC(C)=CC(N)=C1.CC1=CC=C(N)C=C1C.CC1=CC=CC(N)=C1C.CC1=CC=CC(C)=C1N CDULGHZNHURECF-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
- JUVSRZCUMWZBFK-UHFFFAOYSA-N 2-[n-(2-hydroxyethyl)-4-methylanilino]ethanol Chemical compound CC1=CC=C(N(CCO)CCO)C=C1 JUVSRZCUMWZBFK-UHFFFAOYSA-N 0.000 description 1
- OJPDDQSCZGTACX-UHFFFAOYSA-N 2-[n-(2-hydroxyethyl)anilino]ethanol Chemical compound OCCN(CCO)C1=CC=CC=C1 OJPDDQSCZGTACX-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- PJCNYQIIQZWBGS-UHFFFAOYSA-N 4-butyl-n,n-dimethylaniline Chemical compound CCCCC1=CC=C(N(C)C)C=C1 PJCNYQIIQZWBGS-UHFFFAOYSA-N 0.000 description 1
- LVIXJLIXKMZERD-UHFFFAOYSA-N 4-chloro-n,n-diethylaniline Chemical compound CCN(CC)C1=CC=C(Cl)C=C1 LVIXJLIXKMZERD-UHFFFAOYSA-N 0.000 description 1
- SFAHTJULMBNOGW-UHFFFAOYSA-N 4-tert-butyl-n,n-diethylaniline Chemical compound CCN(CC)C1=CC=C(C(C)(C)C)C=C1 SFAHTJULMBNOGW-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 239000004803 Di-2ethylhexylphthalate Substances 0.000 description 1
- IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 description 1
- VOWAEIGWURALJQ-UHFFFAOYSA-N Dicyclohexyl phthalate Chemical compound C=1C=CC=C(C(=O)OC2CCCCC2)C=1C(=O)OC1CCCCC1 VOWAEIGWURALJQ-UHFFFAOYSA-N 0.000 description 1
- IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 description 1
- ZVFDTKUVRCTHQE-UHFFFAOYSA-N Diisodecyl phthalate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC(C)C ZVFDTKUVRCTHQE-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 230000002292 Radical scavenging effect Effects 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 150000001555 benzenes Chemical group 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- JBSLOWBPDRZSMB-BQYQJAHWSA-N dibutyl (e)-but-2-enedioate Chemical compound CCCCOC(=O)\C=C\C(=O)OCCCC JBSLOWBPDRZSMB-BQYQJAHWSA-N 0.000 description 1
- JBSLOWBPDRZSMB-FPLPWBNLSA-N dibutyl (z)-but-2-enedioate Chemical compound CCCCOC(=O)\C=C/C(=O)OCCCC JBSLOWBPDRZSMB-FPLPWBNLSA-N 0.000 description 1
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
- 229960001826 dimethylphthalate Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 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
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- JDEJGVSZUIJWBM-UHFFFAOYSA-N n,n,2-trimethylaniline Chemical compound CN(C)C1=CC=CC=C1C JDEJGVSZUIJWBM-UHFFFAOYSA-N 0.000 description 1
- YQYUUNRAPYPAPC-UHFFFAOYSA-N n,n-diethyl-2-methylaniline Chemical compound CCN(CC)C1=CC=CC=C1C YQYUUNRAPYPAPC-UHFFFAOYSA-N 0.000 description 1
- XNTUJOTWIMFEQS-UHFFFAOYSA-N octadecanoyl octadecaneperoxoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCCCCCCCC XNTUJOTWIMFEQS-UHFFFAOYSA-N 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 230000002250 progressing effect Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000007934 α,β-unsaturated carboxylic acids Chemical class 0.000 description 1
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
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
- C04B41/46—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with organic materials
- C04B41/48—Macromolecular compounds
- C04B41/483—Polyacrylates
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Aftertreatments Of Artificial And Natural Stones (AREA)
- Manufacturing Of Tubular Articles Or Embedded Moulded Articles (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
この発明はコンクリート構造物、コンクリート床、コン
クリート製品など、特にヒユーム管にアクリル系樹脂を
ライニングする方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a method for lining concrete structures, concrete floors, concrete products, etc., particularly humid pipes, with acrylic resin.
コンクリート製のヒユーム管の内壁に樹脂をライニング
することが行われている。このようなライニングにアク
リル系樹脂を使用する場合、一般にアクリル糸上ツマ−
に硬化促進剤を溶解した液に1重合開始剤を混合してラ
イニングを行っている。The inner walls of concrete hume pipes are lined with resin. When using acrylic resin for such linings, acrylic thread tops are generally used.
Lining is performed by mixing a polymerization initiator into a solution in which a curing accelerator is dissolved.
ところがこのようなライニング方法においては、重合開
始剤を混合後、約15分間で硬化が起こるため、1回ラ
イニングを行うごとに、直ちに機器の洗浄を行う必要が
あり、作業性が悪いという問題点があった。However, in this lining method, curing occurs in about 15 minutes after mixing the polymerization initiator, so it is necessary to clean the equipment immediately after each lining, resulting in poor workability. was there.
また重合開始剤を溶剤や可塑剤に溶解して、硬化促進剤
を溶解したモノマーと混合する方法もあるが、この場合
溶剤や可塑剤の量が多くなり、ライニング層の強度が弱
くなるという問題点があった。Another method is to dissolve the polymerization initiator in a solvent or plasticizer and mix it with the monomer in which the curing accelerator is dissolved, but in this case there is a problem that the amount of solvent or plasticizer increases and the strength of the lining layer becomes weaker. There was a point.
本発明の目的は、上記問題点を解決するため、簡単な操
作により能率よくライニングを行うことができ、優れた
強度を有するライニング層を得ることができ、しかも洗
浄も容易で作業性に優れたアクリル系樹脂のライニング
方法を提案することである。The purpose of the present invention is to solve the above-mentioned problems by making it possible to efficiently perform lining with simple operations, to obtain a lining layer with excellent strength, and to provide a lining layer that is easy to clean and has excellent workability. The purpose of this invention is to propose a lining method for acrylic resin.
本発明は、(メタ)アクリル酸およびそのエステルから
選ばれる少なくとも1種のモノマー成分、およびこのモ
ノマー成分に溶解もしくは膨潤可能な重合体からなる樹
脂液を2液に分割し、一方の液に重合開始剤を溶解し、
他方の液に硬化促進剤を溶解し、両液を混合してライニ
ングを行うことを特徴とするアクリル系樹脂のライニン
グ方法である。In the present invention, a resin liquid consisting of at least one monomer component selected from (meth)acrylic acid and its ester and a polymer that can be dissolved or swelled in this monomer component is divided into two liquids, and one liquid is polymerized. Dissolve the initiator,
This is an acrylic resin lining method characterized by dissolving a curing accelerator in the other liquid and mixing both liquids to perform lining.
本発明においてライニングの対象となるのは、ヒユーム
管、コンクリート構造物、コンクリート床、コンクリー
ト製品、その他任意のものがある。In the present invention, objects to be lined include humid pipes, concrete structures, concrete floors, concrete products, and other arbitrary objects.
本発明で使用するアクリル系樹脂としては、(メタ)ア
クリル酸およびそのエステルから選ばれる少なくとも1
alのモノマー成分に、このモノマー成分に溶解もしく
は膨潤可能な重合体を配合したものが使用できる。The acrylic resin used in the present invention includes at least one selected from (meth)acrylic acid and its ester.
It is possible to use a monomer component of al mixed with a polymer that can be dissolved or swelled in this monomer component.
このようなアクリル系樹脂の一例として、たとえば、(
a)(メタ)アクリル酸および/またはそのエステルの
モノマーと、 (b)前記モノマー成分に溶解もしくは
膨潤可能な重合体と、(c)前記モノマー成分に溶解す
る可塑剤と、(d)1分子中に少なくとも2個の重合性
不飽和結合を有する化合物とからなるものが例示できる
。このうち(a)、 (b)成分は必須成分であり、
(c)、 (d)成分は好ましい配合成分である。As an example of such acrylic resin, for example, (
a) a monomer of (meth)acrylic acid and/or its ester; (b) a polymer that can dissolve or swell in the monomer component; (c) a plasticizer that dissolves in the monomer component; and (d) one molecule. Examples include compounds having at least two polymerizable unsaturated bonds therein. Of these, components (a) and (b) are essential components,
Components (c) and (d) are preferred ingredients.
(a)のモノマーとしては、アクリル酸メチル、アクリ
ル酸エチル、メタクリル酸メチル、メタクリル酸エチル
、アクリル酸ブチル(ノルマル、イソ)、メタクリル酸
ブチル(ノルマル、イソ)などの(メタ)アクリル酸ア
ルキル、アクリル酸、メタクリル酸、アクリル酸2−ヒ
ドロキシエチル、メタクリル−2−ヒドロキシエチル、
エチレングリコールジ(メタ)アクリレート、プロピ
レングリコールジ(メタ)アクリレート、ポリエチレン
グリコールジ(メタ)アクリレート、ポリプロピレング
リコールジ(メタ)アクリレート、ブチレングリコール
ジ(メタ)アクリレート、ヘキシレングリコールジ(メ
タ)アクリレート、2,2−ビス〔4−(メタ)アクリ
ロイルオキシフェニル〕プロパン、2,2−ビス〔4−
(メタ)アクリロイルオキシシクロヘキシル〕プロパン
、2,2−ビス〔3−(メタ)アクリロイルオキシ−2
−ヒドロキシプロポキシフェニル〕プロパン、トリメチ
ロールプロパントリ(メタ)アクリレート、ペンタエリ
スリトールテトラ(メタ)アクリレート、ジペンタエリ
スリトールヘキサ(メタ)アクリレートなどを例示する
ことができる。Monomers (a) include alkyl (meth)acrylates such as methyl acrylate, ethyl acrylate, methyl methacrylate, ethyl methacrylate, butyl acrylate (normal, iso), butyl methacrylate (normal, iso), Acrylic acid, methacrylic acid, 2-hydroxyethyl acrylate, methacrylic-2-hydroxyethyl,
Ethylene glycol di(meth)acrylate, propylene glycol di(meth)acrylate, polyethylene glycol di(meth)acrylate, polypropylene glycol di(meth)acrylate, butylene glycol di(meth)acrylate, hexylene glycol di(meth)acrylate, 2 , 2-bis[4-(meth)acryloyloxyphenyl]propane, 2,2-bis[4-
(meth)acryloyloxycyclohexyl]propane, 2,2-bis[3-(meth)acryloyloxy-2
Examples include -hydroxypropoxyphenyl]propane, trimethylolpropane tri(meth)acrylate, pentaerythritol tetra(meth)acrylate, and dipentaerythritol hexa(meth)acrylate.
(b)の重合体としては上記のモノマー特に(メタ)ア
クリル酸エステルの単独または共重合体が例示できる。Examples of the polymer (b) include monopolymers or copolymers of the above-mentioned monomers, particularly (meth)acrylic acid esters.
可塑剤(C)としては、 ジメチルフタレート、ジブチ
ルフタレート、ジシクロへキシルフタレート、ジオクチ
ルフタレート、ジオクチルフタレート、 ジー2−エチ
ルへキシルフタレート、ジイソデシルフタレート、ジブ
チルベンジルフタレートなどのフタル酸エステルを代表
としてあげることができる。Representative examples of the plasticizer (C) include phthalate esters such as dimethyl phthalate, dibutyl phthalate, dicyclohexyl phthalate, dioctyl phthalate, dioctyl phthalate, di-2-ethylhexyl phthalate, diisodecyl phthalate, and dibutylbenzyl phthalate. can.
またジエチルマレエート、ジブチルマレエート、ジオク
チルマレエート、ジブチルフマレート、ジオクチルフマ
レート等の(a)と共重合可能なα、β−不飽和カルボ
ン酸エステルのような内部可塑剤もあげることができる
。Also included are internal plasticizers such as α,β-unsaturated carboxylic acid esters that can be copolymerized with (a) such as diethyl maleate, dibutyl maleate, dioctyl maleate, dibutyl fumarate, and dioctyl fumarate. .
(d)の重合性不飽和結合化合物の代表的なものは、
エチレングリコールジ(メタ)アクリレート。Typical polymerizable unsaturated bond compounds (d) are:
Ethylene glycol di(meth)acrylate.
1.2−プロピレングリコールジ(メタ)アクリレート
。1.2-Propylene glycol di(meth)acrylate.
1.3−ブチレングリコールジ(メタ)アクリレートな
どのアルカンジオールジ(メタ)アクリレート、2.2
−ビス〔3−(メタ)アクリロイルオキシ−2−ヒドロ
キシプロポキシフェニル〕プロパンや昭和高分子(株)
[の商品名リポキシVR−60またはリポキシVR−9
0などのエポキシ樹脂の(メタ)アクリル酸変性物が例
示できる。1. Alkanediol di(meth)acrylates such as 3-butylene glycol di(meth)acrylate, 2.2
-Bis[3-(meth)acryloyloxy-2-hydroxypropoxyphenyl]propane and Showa Kobunshi Co., Ltd.
[Product name: Lipoxy VR-60 or Lipoxy VR-9
Examples include (meth)acrylic acid modified products of epoxy resins such as No. 0.
一般にこれらの各成分の配合割合は、(a)のモノマー
成分が45〜85重量%、(b)の重合体が5〜20重
址%、(c)の可塑剤が1〜25重量%、残部が(d)
からなるのが好ましい。Generally, the blending ratio of each of these components is (a) 45 to 85% by weight of the monomer component, 5 to 20% by weight of the polymer (b), 1 to 25% by weight of the plasticizer (c), The remainder is (d)
It is preferable to consist of
本発明では上記(a)〜(d)成分からなる樹脂液を2
液に分割し、一方の液に重合開始剤を溶解し。In the present invention, the resin liquid consisting of the above components (a) to (d) is
Divide into two liquids and dissolve the polymerization initiator in one liquid.
他方の液に常温硬化を促進する硬化促進剤を溶解する。A curing accelerator that promotes curing at room temperature is dissolved in the other liquid.
(b)〜(d)成分はいずれか一方の液に溶解してもよ
く、また両方の液に溶解してもよい、2分割する液の容
量比は、重合開始剤または硬化促進剤を溶解できる範囲
であれば任意に選択できる。Components (b) to (d) may be dissolved in either one of the liquids, or in both liquids.The volume ratio of the two liquids should be adjusted to dissolve the polymerization initiator or curing accelerator. You can choose as much as you like as long as you can.
重合開始剤としては、ジアシルペルオキシド。Diacyl peroxide is used as a polymerization initiator.
アルキルペルオキシド、アラルキルペルオキシド。Alkyl peroxide, aralkyl peroxide.
過酸、過酸エステルなどの過酸化物、アゾ系化合物など
を使用することができるが、これらのうちではジアシル
ペルオキシドを使用するのが好ましい。ジアシルペルオ
キシドとして具体的には、ジベンゾイルペルオキシド、
ジアセチルペルオキシド、シカプリルペルオキシド、ジ
ラウロイルペルオキシド、ジステアロイルペルオキシド
などを例示することができる。Peroxides such as peracids and peracid esters, azo compounds, and the like can be used, but among these, diacyl peroxides are preferably used. Specifically, diacyl peroxides include dibenzoyl peroxide,
Examples include diacetyl peroxide, cicapril peroxide, dilauroyl peroxide, and distearoyl peroxide.
硬化促進剤として使用するアミン類としては第一アミン
、第三アミンのいずれでも使用することができるが、第
三アミンが好適に使用される。As the amines used as the curing accelerator, either primary amines or tertiary amines can be used, but tertiary amines are preferably used.
具体的には、アニリン、トルイジン、キシリジン。Specifically, aniline, toluidine, and xylidine.
フェニレンジアミン、 N、N−ジメチルアニリン、N
。Phenyldiamine, N,N-dimethylaniline, N
.
N−ジエチルアニリン、N、N−ジ(β−ヒドロキシエ
チル)アニリン、N、N−ジメチルトルイジン、N、N
−ジエチルトルイジン、N、N−ジメチルアニシジン、
N。N-diethylaniline, N,N-di(β-hydroxyethyl)aniline, N,N-dimethyltoluidine, N,N
-diethyltoluidine, N,N-dimethylanisidine,
N.
N−ジエチルアニシジン、 N、N−ジメチル−p−
t−ブチルアニリン、N、N−ジエチル−p−t−ブチ
ルアニリン、N、N−ジエチル−p−クロルアニリン、
ジフェニルアミン、 N、N−(β−ヒドロキシエチ
ル)−p−トルイジンなどを例示することができる。こ
れらの中では、N、N−ジメチル−p−トルイジン、N
、N−ジメチル−p−ブチルアニリン、N、N−ジメチ
ルアニシジン、N、N−ジメチルードクロルアニリン、
N、N−ビス(β−ヒドロキシエチル)−p−トルイジ
ンなどの少なくともベンゼン類の2位に電子供与体の置
換基を有する第三アミンが好ましく、 N、N−ジメ
チル−p−トルイジン。N-diethylanisidine, N,N-dimethyl-p-
t-butylaniline, N,N-diethyl-p-t-butylaniline, N,N-diethyl-p-chloroaniline,
Examples include diphenylamine, N,N-(β-hydroxyethyl)-p-toluidine, and the like. Among these, N,N-dimethyl-p-toluidine, N
, N-dimethyl-p-butylaniline, N,N-dimethylanisidine, N,N-dimethyldochloroaniline,
Tertiary amines having an electron donor substituent at least at the 2-position of benzenes are preferred, such as N,N-bis(β-hydroxyethyl)-p-toluidine, and N,N-dimethyl-p-toluidine.
N、N−ジメチル−p−t−ブチルアニリンが特に好ま
しい。Particularly preferred is N,N-dimethyl-p-t-butylaniline.
この重合開始剤および硬化促進剤の樹脂液に対する配合
割合は前記(a)〜(d)よりなる樹脂液io。The blending ratio of the polymerization initiator and curing accelerator to the resin liquid is the resin liquid io consisting of the above (a) to (d).
重量部に対して概ね前者が0.1〜20ji1部、後者
が0.1〜20重景部重電る。The former is approximately 0.1 to 20 parts by weight, and the latter is approximately 0.1 to 20 parts by weight.
また、空気中の酸素によるラジカル捕捉により表面の硬
化反応が十分進まない事を無くすため固体のパラフィン
、好ましくは融点40〜60℃のパラフィンワックスの
添加が好ましい、このパラフィンのレジンモルタルに対
する配合割合は、前記(a)〜(d)よりなる樹脂液1
00重斌重殖対し、0.1〜1.0重量部である。In addition, in order to prevent the surface hardening reaction from progressing sufficiently due to radical scavenging by oxygen in the air, it is preferable to add solid paraffin, preferably paraffin wax with a melting point of 40 to 60°C.The proportion of this paraffin in the resin mortar is , resin liquid 1 consisting of the above (a) to (d)
The amount is 0.1 to 1.0 parts by weight per 0.00 parts by weight.
このほか珪砂、カオリン、タルク、炭酸カルシウム等の
充填剤、および有機顔料、無機顔料等の着色剤を配合す
ることができ、これらはいずれか一方または両方の液に
配合してもよい。In addition, fillers such as silica sand, kaolin, talc, and calcium carbonate, and colorants such as organic pigments and inorganic pigments may be blended, and these may be blended into either or both of the liquids.
ライニング方法は、上記の重合開始剤を溶解した液と硬
化促進剤を溶解した液を混合して吹付け。The lining method involves spraying a mixture of a solution containing the polymerization initiator and a solution containing a curing accelerator.
ライニングを行う。両液の混合はノズル等の吹付装置内
で混合してもよく、また別のノズルから吹付けて混合し
てもよい。Perform lining. The two liquids may be mixed in a spray device such as a nozzle, or may be mixed by spraying from a separate nozzle.
ライニングされたアクリル系樹脂は2液温合後15〜3
0分間で硬化し、ライニング層を形成する。The lined acrylic resin is 15 to 3
It hardens in 0 minutes to form a lining layer.
こうして得られるライニング層は樹脂溶液がヒユーム管
の割れ目、すき間等に浸透して硬化するので接着性が良
好であり、またアクリル系モノマーの重合体を含むため
、モノマーのみを重合させる場合に比べて収縮率は小さ
く、また2個の重合性不飽和結合を有する化合物を含む
ため、三次元構造となり強度が大きくなる。The lining layer obtained in this way has good adhesion because the resin solution penetrates into the cracks and gaps of the fume tube and hardens, and since it contains a polymer of acrylic monomer, it has better adhesion than when only the monomer is polymerized. The shrinkage rate is small, and since it contains a compound having two polymerizable unsaturated bonds, it has a three-dimensional structure and has high strength.
ライニング作業後は2液の混合部以後の部分を洗浄すれ
ばよく、他の部分は長時間継続して使用することができ
、作業性は優れている。After the lining work, it is only necessary to wash the part after the mixing part of the two liquids, and the other parts can be used continuously for a long time, and the workability is excellent.
以下、本発明の実施例を図面に基づいて説明する。 Embodiments of the present invention will be described below based on the drawings.
メチルメタクリレート70重電部、ポリメチルメタクリ
レート20重址部、l、4−ブチレングリコールジメタ
クリレート5重量部、およびジシクロへキシ重殖タシー
85重景部からなる樹脂液を1:1に分割し、一方のA
液に重合開始剤としてジアシルペルオキシドを3重社部
、他方のB液に硬化促進剤としてN、N−ジメチル−p
−トルイジンを3重量部溶解した。A resin liquid consisting of 70 parts by weight of methyl methacrylate, 20 parts by weight of polymethyl methacrylate, 5 parts by weight of l,4-butylene glycol dimethacrylate, and 85 parts by weight of dicyclohexy-polymers is divided in a ratio of 1:1, One A
Diacyl peroxide was added to the solution as a polymerization initiator, and N,N-dimethyl-p was added to the other B solution as a curing accelerator.
- 3 parts by weight of toluidine was dissolved.
第1図は実施例のライニング方法を示す系統図である0
図において、1.2は溶解タンクで、それぞれA液およ
びB液を溶解しておく、これらのA液およびB液をポン
プ3.4によりライン5゜6からノズル7に供給し、ノ
ズル7内で混合してヒユーム管8内に吹付けてライニン
グを行う。FIG. 1 is a system diagram showing the lining method of the embodiment.
In the figure, 1.2 is a dissolution tank in which liquids A and B are dissolved respectively.These liquids A and B are supplied to the nozzle 7 from the line 5゜6 by a pump 3.4, and are fed into the nozzle 7. The mixture is mixed and sprayed into the fume pipe 8 for lining.
こうして得られたライニング層は接着性が良好で1強度
、耐候性等に優れ、長期間にわたってヒユーム管の内面
を保護することができる。The lining layer thus obtained has good adhesion, excellent strength, weather resistance, etc., and can protect the inner surface of the humid tube for a long period of time.
ライニング後は、硬化前にノズル7のみを洗浄すればよ
く、他の部分は継続して使用可能である。After lining, only the nozzle 7 needs to be cleaned before curing, and the other parts can be used continuously.
本発明によれば、簡単な操作により能率よくアクリル系
樹脂のライニングを行うことができ、優れた強度を有す
るライニング層を形成することができ、しかも洗浄が容
易で、作業性に優れている。According to the present invention, acrylic resin lining can be performed efficiently with simple operations, a lining layer with excellent strength can be formed, and furthermore, it is easy to clean and has excellent workability.
【図面の簡単な説明】
第1図は実施例の系統図である。
1.2は溶解タンク、3.4はポンプ、7はノズル、8
はヒユーム管である。
代理人 弁理士 柳 原 成
3.4:ポンプ
7:ノズル
8:bz−、−警BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a system diagram of an embodiment. 1.2 is the dissolution tank, 3.4 is the pump, 7 is the nozzle, 8
is Huyum's canal. Agent Patent Attorney Sei Yanagihara 3.4: Pump 7: Nozzle 8: bz-, - Police
Claims (1)
れる少なくとも1種のモノマー成分、およびこのモノマ
ー成分に溶解もしくは膨潤可能な重合体からなる樹脂液
を2液に分割し、一方の液に重合開始剤を溶解し、他方
の液に硬化促進剤を溶解し、両液を混合してライニング
を行うことを特徴とするアクリル系樹脂のライニング方
法。(1) A resin liquid consisting of at least one monomer component selected from (meth)acrylic acid and its ester and a polymer that can be dissolved or swelled in this monomer component is divided into two liquids, and one liquid starts polymerization. A method for lining an acrylic resin, characterized by dissolving a hardening agent in the other liquid, dissolving a curing accelerator in the other liquid, and mixing both liquids to perform lining.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63105672A JP2581152B2 (en) | 1988-04-28 | 1988-04-28 | Acrylic resin lining method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63105672A JP2581152B2 (en) | 1988-04-28 | 1988-04-28 | Acrylic resin lining method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01278482A true JPH01278482A (en) | 1989-11-08 |
JP2581152B2 JP2581152B2 (en) | 1997-02-12 |
Family
ID=14413930
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63105672A Expired - Lifetime JP2581152B2 (en) | 1988-04-28 | 1988-04-28 | Acrylic resin lining method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2581152B2 (en) |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS523631A (en) * | 1975-05-28 | 1977-01-12 | Kansai Paint Co Ltd | Coating composition |
JPS53127542A (en) * | 1977-04-13 | 1978-11-07 | Denki Kagaku Kogyo Kk | Coating of two-pack type acrylic adhesive and its device |
JPS53135190A (en) * | 1977-04-27 | 1978-11-25 | Denki Kagaku Kogyo Kk | Lamp |
JPS5834513A (en) * | 1981-08-25 | 1983-03-01 | 日立電線株式会社 | Method of producing highly foamable insulated wire |
JPS58196268A (en) * | 1982-05-12 | 1983-11-15 | Mitsubishi Rayon Co Ltd | Floor-and wall-coating or road-marking composition |
JPS60251975A (en) * | 1984-05-28 | 1985-12-12 | Kubota Ltd | Method for painting inner surface of pipe |
JPS6223482A (en) * | 1985-07-19 | 1987-01-31 | Osaka Bosui Kensetsushiya:Kk | Method for coating inner surface of pipeline |
JPS638152A (en) * | 1986-06-24 | 1988-01-13 | Dainippon Printing Co Ltd | Automatic splicer for rotary press |
-
1988
- 1988-04-28 JP JP63105672A patent/JP2581152B2/en not_active Expired - Lifetime
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS523631A (en) * | 1975-05-28 | 1977-01-12 | Kansai Paint Co Ltd | Coating composition |
JPS53127542A (en) * | 1977-04-13 | 1978-11-07 | Denki Kagaku Kogyo Kk | Coating of two-pack type acrylic adhesive and its device |
JPS53135190A (en) * | 1977-04-27 | 1978-11-25 | Denki Kagaku Kogyo Kk | Lamp |
JPS5834513A (en) * | 1981-08-25 | 1983-03-01 | 日立電線株式会社 | Method of producing highly foamable insulated wire |
JPS58196268A (en) * | 1982-05-12 | 1983-11-15 | Mitsubishi Rayon Co Ltd | Floor-and wall-coating or road-marking composition |
JPS60251975A (en) * | 1984-05-28 | 1985-12-12 | Kubota Ltd | Method for painting inner surface of pipe |
JPS6223482A (en) * | 1985-07-19 | 1987-01-31 | Osaka Bosui Kensetsushiya:Kk | Method for coating inner surface of pipeline |
JPS638152A (en) * | 1986-06-24 | 1988-01-13 | Dainippon Printing Co Ltd | Automatic splicer for rotary press |
Also Published As
Publication number | Publication date |
---|---|
JP2581152B2 (en) | 1997-02-12 |
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