JP2544891B2 - Ballast fixing method - Google Patents
Ballast fixing methodInfo
- Publication number
- JP2544891B2 JP2544891B2 JP5222641A JP22264193A JP2544891B2 JP 2544891 B2 JP2544891 B2 JP 2544891B2 JP 5222641 A JP5222641 A JP 5222641A JP 22264193 A JP22264193 A JP 22264193A JP 2544891 B2 JP2544891 B2 JP 2544891B2
- Authority
- JP
- Japan
- Prior art keywords
- ballast
- resin
- aqueous
- water
- spraying
- 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.)
- Expired - Fee Related
Links
- 238000000034 method Methods 0.000 title claims description 29
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- 239000011347 resin Substances 0.000 claims description 63
- 238000005507 spraying Methods 0.000 claims description 22
- 230000004931 aggregating effect Effects 0.000 claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 26
- 239000000839 emulsion Substances 0.000 description 17
- 239000000243 solution Substances 0.000 description 13
- 239000000178 monomer Substances 0.000 description 11
- 239000007864 aqueous solution Substances 0.000 description 10
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 239000007921 spray Substances 0.000 description 6
- 239000000701 coagulant Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000004575 stone Substances 0.000 description 5
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- -1 polyoxyethylene Polymers 0.000 description 4
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- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 239000004568 cement Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
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- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
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- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 229920006397 acrylic thermoplastic Polymers 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 239000012874 anionic emulsifier Substances 0.000 description 2
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- 230000000052 comparative effect Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 238000007720 emulsion polymerization reaction Methods 0.000 description 2
- 238000003912 environmental pollution Methods 0.000 description 2
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- 229910052757 nitrogen Inorganic materials 0.000 description 2
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- 230000000704 physical effect Effects 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- XUDBVJCTLZTSDC-UHFFFAOYSA-N 2-ethenylbenzoic acid Chemical compound OC(=O)C1=CC=CC=C1C=C XUDBVJCTLZTSDC-UHFFFAOYSA-N 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide 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
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- BCZXFFBUYPCTSJ-UHFFFAOYSA-L Calcium propionate Chemical compound [Ca+2].CCC([O-])=O.CCC([O-])=O BCZXFFBUYPCTSJ-UHFFFAOYSA-L 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000002211 L-ascorbic acid Substances 0.000 description 1
- 235000000069 L-ascorbic acid Nutrition 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical class CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical class C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
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- VSGNNIFQASZAOI-UHFFFAOYSA-L calcium acetate Chemical compound [Ca+2].CC([O-])=O.CC([O-])=O VSGNNIFQASZAOI-UHFFFAOYSA-L 0.000 description 1
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- 235000011092 calcium acetate Nutrition 0.000 description 1
- 229960005147 calcium acetate Drugs 0.000 description 1
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- 235000010331 calcium propionate Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
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- 238000005056 compaction Methods 0.000 description 1
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- SPTHWAJJMLCAQF-UHFFFAOYSA-M ctk4f8481 Chemical compound [O-]O.CC(C)C1=CC=CC=C1C(C)C SPTHWAJJMLCAQF-UHFFFAOYSA-M 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 235000001727 glucose Nutrition 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- UEGPKNKPLBYCNK-UHFFFAOYSA-L magnesium acetate Chemical compound [Mg+2].CC([O-])=O.CC([O-])=O UEGPKNKPLBYCNK-UHFFFAOYSA-L 0.000 description 1
- 239000011654 magnesium acetate Substances 0.000 description 1
- 235000011285 magnesium acetate Nutrition 0.000 description 1
- 229940069446 magnesium acetate Drugs 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 235000011147 magnesium chloride Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
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- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
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- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
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- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
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- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
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- 238000007790 scraping Methods 0.000 description 1
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- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
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- 229940035048 sorbitan monostearate Drugs 0.000 description 1
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- 238000005728 strengthening Methods 0.000 description 1
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- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- CNALVHVMBXLLIY-IUCAKERBSA-N tert-butyl n-[(3s,5s)-5-methylpiperidin-3-yl]carbamate Chemical compound C[C@@H]1CNC[C@@H](NC(=O)OC(C)(C)C)C1 CNALVHVMBXLLIY-IUCAKERBSA-N 0.000 description 1
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Landscapes
- Railway Tracks (AREA)
- Machines For Laying And Maintaining Railways (AREA)
Description
【0001】[0001]
【産業上の利用分野】この発明は、鉄道線路の道床バラ
ストなど、バラストを固着する方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for fixing ballast, such as ballast ballast on railroad tracks.
【0002】[0002]
【従来の技術】従来、鉄道線路としては、路盤上に砕石
や砂利等のバラストで作られた道床を置き、さらにその
上に枕木を置いてレールを締結した構造を持つもの、い
わゆる有道床軌道が大部分を占めている。前記バラスト
で作られた道床には、枕木から伝わる列車加重を分散し
て下部の路盤に伝えたり、列車通過時の振動を吸収した
りする役割がある。2. Description of the Related Art Conventionally, a railroad track has a structure in which a roadbed made of ballast such as crushed stone or gravel is placed on the roadbed, and sleepers are further placed on it to fasten rails, that is, a so-called roadbed track. Occupy most. The ballast made of the ballast has a role of dispersing the train load transmitted from the sleepers and transmitting it to the lower roadbed and absorbing vibrations when the train passes.
【0003】しかし、バラストを用いた道床には、たと
えば、下記〜の問題があった。 バラスト崩れ…道床は、列車の通過により数10H
z以上の振動を繰り返し受けている。この振動により、
バラストの圧密状態が弛緩して崩れてくるため、補修作
業を行う必要がある。特に、線路の曲線部分において
は、列車の走行安全性を保持するために、外側のレール
を内側のレールより高くした「カント」をつけているの
で、前記のような振動を受けた砕石等が線路外側の高い
部分から線路内側の低い部分へ移動して、バラストが経
時的に崩れてくる。その結果、枕木の列車横圧に対する
抵抗力が減少して、危険な状態になる。このため、平坦
部では、通常1年以上の間、補修の必要がないのに対
し、曲線部では、短期間での補修が必要となる。また、
バラスト軌道は、列車の通過に伴い、軌道ぐるいが発生
するため、スラブ軌道等のコンクリート道床に比べ、短
期間で補修作業が必要となる。However, the ballast using a ballast has the following problems, for example. Ballast collapses ... The roadbed is several tens of hours due to passing trains.
Repeated vibration of z or more. Due to this vibration,
It is necessary to perform repair work because the compacted state of the ballast loosens and collapses. In particular, in the curved part of the track, in order to maintain the running safety of the train, the outer rail is attached with a "cant" that is higher than the inner rail, so crushed stones etc. that have been subjected to the above-mentioned vibration The ballast collapses over time, moving from the high part outside the track to the low part inside the track. As a result, the resistance of the sleepers to the rolling stock lateral pressure is reduced, resulting in a dangerous condition. For this reason, the flat part usually does not need to be repaired for one year or more, whereas the curved part needs to be repaired in a short period of time. Also,
Ballast tracks have a roundabout shape as the train passes, so repair work is required in a shorter period than concrete slab tracks such as slab tracks.
【0004】 雪害によるバラスト飛散…冬季に積雪
等のある寒冷地では、列車に雪塊(氷塊)が付着するこ
とが多い。列車に付着した雪塊(氷塊)は、温暖地への
列車の移動に伴って融解し落下して、バラストに衝突す
る。特に、列車走行時であれば、その衝撃は、一時的で
はあるが極めて大きいものであるため、バラストが飛散
して周辺の民家や駐車中の自動車等に被害を与える。Ballast scattering due to snow damage ... In cold regions where there is snow in winter, snow blocks (ice blocks) often adhere to trains. The snow mass (ice mass) attached to the train melts and falls as the train moves to a warm area, and collides with the ballast. In particular, when the train is running, the impact is temporary but extremely large, and the ballast scatters, damaging surrounding private houses and parked cars.
【0005】 風圧によるバラスト飛散…列車が高速
(たとえば、時速200km以上)で道床上を通過する
場合、道床の表層部分が、列車の風圧で浮き上がり、真
上を通過している列車に衝突して、砕石等が飛散する。
この飛散した砕石等は、通過中の列車と同程度の速度を
有しているため、沿線の民家や駐車中の自動車等に被害
を与えたり、ホーム上で列車を待つ乗客や線路を点検す
る保線従事者等に危害を与えたりする危険性がある。Ballast scattering due to wind pressure: When a train passes over the roadbed at a high speed (for example, 200 km / h or more), the surface layer of the roadbed floats up due to the wind pressure of the train and collides with a train passing directly above. , Crushed stones are scattered.
Since the scattered crushed stones have the same speed as a passing train, they may damage the private houses along the line or parked cars, and inspect passengers and tracks waiting for the train on the platform. There is a risk of harming track maintenance workers.
【0006】従来、このような道床の問題を解消するた
めの方法としては、たとえば、下記(1)〜(3)の方
法があった。 (1)ゴムラテックス、合成樹脂、およびセメントを混
合した薬液を散布してバラストを固結することによっ
て、バラスト飛散を防止したり、バラスト道床を強化し
たりする方法(特開昭49−32306号公報、特開昭
52−16810号公報等参照)。Conventionally, as a method for solving the problem of such a roadbed, there have been, for example, the following methods (1) to (3). (1) A method of preventing ballast scattering or strengthening a ballast ballast by spraying a chemical solution in which rubber latex, synthetic resin, and cement are mixed to consolidate the ballast (JP-A-49-32306). Japanese Patent Laid-Open Publication No. 52-16810, etc.).
【0007】(2)バラスト飛散防止用にネットを張る
方法。 (3)バラストを用いずに、コンクリートやアスファル
トを用いて道床を形成する方法。 ところが、前記(1)の方法は、セメント硬化速度制御
の困難さ、コストの高さ、薬液散布後のセメントの硬さ
によるバラストの保線作業の困難さ、等の理由から、現
在ほとんど行われていない。(2) A method of setting a net for preventing ballast scattering. (3) A method of forming a ballast using concrete or asphalt without using ballast. However, the method (1) is currently mostly used for reasons such as difficulty in controlling the rate of hardening of cement, high cost, and difficulty in keeping track of ballast due to hardness of cement after spraying a chemical solution. Absent.
【0008】また、前記(2)の方法は、ネットを張っ
たり除去したりする作業の困難さ、コストの高さ、列車
のネット巻き込みによる事故発生の危険性、等の理由か
ら、一部にしか行われていない。さらに、前記(3)の
方法は、コストが非常に高いため、ごく一部にしか行わ
れていない。Further, the method (2) is partly due to the reasons such as difficulty in attaching and removing the net, high cost, and risk of accident due to train being caught in the net. Only done. Furthermore, the method (3) is very expensive, and thus only partially performed.
【0009】これらの問題を解決する方法として、水性
樹脂からなるバラスト固着用薬液(以下、これを単に
「水性樹脂」と称することがある。)を散布する方法が
開発された。すなわち、水性樹脂をバラスト上に散布
し、水性樹脂をバラスト間に浸透させた後、自然乾燥さ
せて成膜させることにより、バラスト同士を固着させる
方法である。As a method for solving these problems, a method has been developed in which a ballast-fixing chemical liquid composed of an aqueous resin (hereinafter, simply referred to as "aqueous resin") is sprayed. That is, it is a method of fixing the ballasts by spraying the aqueous resin on the ballast, allowing the aqueous resin to permeate between the ballasts, and then naturally drying to form a film.
【0010】この方法によれば、バラストを用いた道床
の列車加重分散性、振動吸収性、多孔性、排水性、等を
阻害することなく、バラスト崩れ、雪害や風圧によるバ
ラスト飛散、等を防止することができるとともに、散布
作業が容易で安価であり、バラストの突き固め、掻き崩
し、掻き均し等の保線作業にも支障のない程度の固着力
を有する皮膜を形成することができる。According to this method, it is possible to prevent ballast collapse, snow damage, ballast scattering due to wind pressure, etc., without impairing the train load dispersion, vibration absorption, porosity, drainage, etc. of the roadbed using ballast. In addition, the spraying work is easy and inexpensive, and a film having a fixing force that does not hinder track maintenance work such as ballast compaction, scraping, and leveling can be formed.
【0011】[0011]
【発明が解決しようとする課題】ところが、この水性樹
脂の媒体は、環境公害等の面から、主成分が水であるこ
とが必要である。このため、乾燥前に降雨等があると、
樹脂が流出することから、作業が天候に非常に左右され
やすく、作業日程の調整が困難である。また、バラスト
固着強度は樹脂が乾燥して成膜するまで出ないが、作業
終了直後では、列車の風圧によるバラスト飛散防止に十
分な固着強度が出ない。However, the medium of the aqueous resin needs to have water as a main component in view of environmental pollution. Therefore, if there is rainfall etc. before drying,
Since the resin flows out, the work is very sensitive to the weather and it is difficult to adjust the work schedule. Further, the ballast fixing strength does not appear until the resin is dried to form a film, but immediately after the work is completed, the fixing strength sufficient to prevent ballast scattering due to the wind pressure of the train does not appear.
【0012】このような事情に鑑み、この発明は、水性
樹脂の散布直後から、降雨等による流出を防止し、風圧
によるバラスト飛散を防止できる程度のバラスト固着強
度を出すことができるバラスト固着方法を提供する。In view of such circumstances, the present invention provides a ballast fixing method capable of preventing the outflow due to rainfall or the like immediately after spraying the water-based resin and providing the ballast fixing strength sufficient to prevent the ballast scattering due to wind pressure. provide.
【0013】[0013]
【課題を解決するための手段】前記課題を解決するた
め、この発明にかかるバラスト固着方法は、バラスト上
に水性樹脂を散布した後、凝集剤水溶液を散布すること
を特徴とするものである。この発明に使用する水性樹脂
としては樹脂エマルジョンおよび水溶性樹脂が例示され
るが、分散媒または溶媒としては、環境公害等の面か
ら、主成分が水であることが必要である。In order to solve the above-mentioned problems, the ballast fixing method according to the present invention is characterized in that an aqueous resin is sprayed on the ballast and then an aqueous flocculant solution is sprayed. Examples of the water-based resin used in the present invention include resin emulsions and water-soluble resins, but the dispersion medium or solvent must be water as a main component from the viewpoint of environmental pollution.
【0014】水性樹脂のイオン性は、特に限定されない
が、凝集剤による凝集性を高めるために、アニオン性で
あることが好ましい。ノニオン性では凝集させにくく、
カチオン性では毒性の不安がある。水性樹脂の使用方法
としては、特に限定はされないが、通常は、如雨露や散
布機等を用い、水性樹脂をバラスト上に散布し、水性樹
脂をバラスト間に浸透させる方法が採られる。風圧によ
るバラスト飛散を防止する上では、水性樹脂は、道床全
体に浸透させなくても構わない。道床の表層部のバラス
トにだけ水性樹脂を浸透させて、バラストを固着させて
も、風圧によるバラスト飛散の防止効果を充分得ること
ができるとともに、低コスト化が図れるからである。The ionicity of the aqueous resin is not particularly limited, but it is preferably anionic in order to enhance the cohesiveness of the coagulant. Nonionic nature makes it difficult to aggregate,
If it is cationic, there is fear of toxicity. The method of using the water-based resin is not particularly limited, but usually, a method of spraying the water-based resin on the ballast using a rain dew or a spraying machine and allowing the water-based resin to permeate between the ballasts is adopted. In order to prevent the ballast from scattering due to wind pressure, the water-based resin does not have to penetrate the entire track. This is because even if the water-based resin is infiltrated only in the ballast of the surface layer of the roadbed to fix the ballast, the effect of preventing the ballast from scattering due to the wind pressure can be sufficiently obtained and the cost can be reduced.
【0015】水性樹脂の粘度は、特に限定されないが、
バラストの表層部分だけ固着させるには、低すぎないほ
うが好ましい。この発明で使用する水性樹脂は、特に限
定されず、例えば、アクリル系、スチレン−アクリル
系、酢酸ビニル−アクリル系、スチレン−ブタジエン
系、酢酸ビニル系、エチレン−酢酸ビニル系、塩化ビニ
リデン系等の水性樹脂を用いることができる。Although the viscosity of the aqueous resin is not particularly limited,
It is preferably not too low for fixing only the surface layer portion of the ballast. The aqueous resin used in the present invention is not particularly limited, and examples thereof include acrylics, styrene-acrylics, vinyl acetate-acrylics, styrene-butadienes, vinyl acetates, ethylene-vinyl acetates, and vinylidene chloride. Aqueous resins can be used.
【0016】この水性樹脂を得る方法としては、特に限
定されず、従来の樹脂エマルジョンあるいは水溶性樹脂
を得る方法と同様の方法を用いることができる。たとえ
ば、エマルジョンをえる方法としては、重合性単量体を
水中で乳化重合させるようにしてもよいし、あるいは、
重合性単量体を乳化重合以外の重合法により重合させて
ポリマーを得た後、そのポリマーを水中に乳濁させるよ
うにしてもよい。また、水溶性樹脂を得る方法として
は、水に溶解しうる溶媒中で重合性単量体を重合させ、
必要により中和後、水に溶解させても良いし、水に不溶
の溶媒中で重合性単量体を重合させた後、溶媒を除去
し、そのポリマーを水に溶解させても良い。重合性単量
体を重合させる際の温度等も、特に限定されない。必要
に応じては、乳化剤や重合開始剤等を適宜用いてもよ
い。The method for obtaining this aqueous resin is not particularly limited, and the same method as that for obtaining a conventional resin emulsion or water-soluble resin can be used. For example, as a method for obtaining an emulsion, a polymerizable monomer may be emulsion polymerized in water, or,
After polymerizing the polymerizable monomer by a polymerization method other than emulsion polymerization to obtain a polymer, the polymer may be emulsified in water. Further, as a method of obtaining a water-soluble resin, by polymerizing a polymerizable monomer in a solvent that can be dissolved in water,
If necessary, it may be dissolved in water after neutralization, or after the polymerizable monomer is polymerized in a solvent insoluble in water, the solvent is removed and the polymer may be dissolved in water. The temperature and the like for polymerizing the polymerizable monomer are not particularly limited. If necessary, an emulsifier, a polymerization initiator or the like may be appropriately used.
【0017】使用する重合性単量体は、特に限定されな
いが、凝集剤の種類によって凝集効率が異なってくる。
たとえば、アルミニウムを含む凝集剤の場合は、重合性
単量体成分全体に対して、カルボキシル基含有単量体を
0.1重量%以上使用することが好ましく、1重量%以
上使用することがより好ましい。上記カルボキシル基含
有重合性単量体としては、アクリル酸、メタクリル酸、
クロトン酸、イタコン酸、フマル酸、マレイン酸、ビニ
ル安息香酸、ケイ皮酸等が挙げられる。また、カルシウ
ムを含む凝集剤の場合は、重合性単量体成分全体に対す
るカルボキシル基含有単量体の使用割合を8重量%以下
にすることが好ましく、4重量%以下にすることがより
好ましい。The polymerizable monomer used is not particularly limited, but the aggregating efficiency varies depending on the type of aggregating agent.
For example, in the case of an aggregating agent containing aluminum, it is preferable to use a carboxyl group-containing monomer in an amount of 0.1% by weight or more, and more preferably 1% by weight or more, based on the entire polymerizable monomer component. preferable. The carboxyl group-containing polymerizable monomer, acrylic acid, methacrylic acid,
Examples thereof include crotonic acid, itaconic acid, fumaric acid, maleic acid, vinylbenzoic acid, cinnamic acid and the like. In the case of a flocculant containing calcium, the proportion of the carboxyl group-containing monomer used with respect to the entire polymerizable monomer component is preferably 8% by weight or less, more preferably 4% by weight or less.
【0018】樹脂エマルジョンを得るために使用する乳
化剤は、特に限定はされない。凝集剤によって効率よく
凝集させるためには、アニオン性乳化剤を使用すること
が好ましいが、ノニオン性乳化剤を併用してもかまわな
い。上記アニオン性乳化剤としては、ドデシルベンゼン
スルホン酸ナトリウム、ドデシル硫酸ナトリウム、ジア
ルキルスルホコハク酸ナトリウム、ポリオキシエチレン
アルキルエーテルサルフェートアンモニウム塩、アルキ
ルエーテル燐酸塩等が挙げられる。上記ノニオン性乳化
剤としては、ポリオキシエチレンノニルフェニルエーテ
ル、ポリエチレングリコールモノステアレート、ソルビ
タンモノステアレート等が挙げられる。The emulsifier used to obtain the resin emulsion is not particularly limited. An anionic emulsifier is preferably used for efficiently aggregating with the aggregating agent, but a nonionic emulsifier may be used in combination. Examples of the anionic emulsifier include sodium dodecylbenzene sulfonate, sodium dodecyl sulfate, sodium dialkyl sulfosuccinate, polyoxyethylene alkyl ether sulfate ammonium salt, alkyl ether phosphate and the like. Examples of the nonionic emulsifier include polyoxyethylene nonyl phenyl ether, polyethylene glycol monostearate, sorbitan monostearate and the like.
【0019】重合開始剤としては、特に限定はされない
が、過硫酸カリウム、過硫酸ナトリウム、過硫酸アンモ
ニウム等の過硫酸塩、クメンハイドロパーオキサイド、
ジイソプロピルベンゼンハイドロパーオキサイド、ベン
ゾイルパーオキサイド等の有機過酸化物、アゾビスイソ
ブチロニトリル等のアゾ系化合物、過酸化水素等を使用
することができる。The polymerization initiator is not particularly limited, but persulfates such as potassium persulfate, sodium persulfate and ammonium persulfate, cumene hydroperoxide,
Organic peroxides such as diisopropylbenzene hydroperoxide and benzoyl peroxide, azo compounds such as azobisisobutyronitrile, hydrogen peroxide and the like can be used.
【0020】水に溶解しうる溶媒としては、エタノー
ル、イソプロピルアルコール、ブチルセロソルブ等のア
ルコール類、ケトン類等を使用することができる。ま
た、乳化重合を促進させるために、ピロ重亜硫酸ナトリ
ウム、亜硫酸ナトリウム、亜硫酸水素ナトリウム、硫酸
第一鉄、グルコース、ホルムアルデヒド、ナトリウムス
ルホキシレート、L−アスコルビン酸等の還元剤を併用
してもよい。As the solvent soluble in water, alcohols such as ethanol, isopropyl alcohol and butyl cellosolve, ketones and the like can be used. Further, in order to promote emulsion polymerization, a reducing agent such as sodium pyrobisulfite, sodium sulfite, sodium hydrogen sulfite, ferrous sulfate, glucose, formaldehyde, sodium sulfoxylate, and L-ascorbic acid may be used in combination. .
【0021】この発明で使用する水性樹脂は、その物性
において特に限定はないが、水性樹脂の散布性、バラス
ト間への浸透性、および乾燥性をよくするためには、下
記の物性を有することが好ましい。水性樹脂の粘度は、
10〜10000cpsであることが好ましい。粘度が
10000cpsを超える場合は、バラスト上に樹脂エ
マルジョンを均一に散布することが困難になることがあ
り、10cps未満では表層付近での歩留まりが悪くな
ることがある。The water-based resin used in the present invention is not particularly limited in its physical properties, but in order to improve the dispersibility of the water-based resin, the permeability between ballasts, and the drying property, it must have the following physical properties. Is preferred. The viscosity of the aqueous resin is
It is preferably 10 to 10,000 cps. If the viscosity exceeds 10,000 cps, it may be difficult to uniformly disperse the resin emulsion on the ballast, and if it is less than 10 cps, the yield near the surface layer may deteriorate.
【0022】水性樹脂の不揮発分濃度は、水性樹脂全体
に対して5重量%以上であることが好ましい。不揮発分
濃度が5重量%未満である場合は、乾燥後、バラストへ
の樹脂付着量が少なくなり過ぎ、所望の防止効果が得ら
れないからである。樹脂エマルジョンの平均粒子径は、
樹脂エマルジョンの乾燥性と粘度に影響を与える。一般
的には、平均粒子径が小さい程、乾燥性が良くなる反
面、粘度が高くなり、樹脂エマルジョンの散布性や浸透
性が悪くなる。そのため、樹脂エマルジョンの平均粒子
径は、10nm〜10μm程度が好ましい。The nonvolatile content of the aqueous resin is preferably 5% by weight or more with respect to the entire aqueous resin. This is because if the nonvolatile content concentration is less than 5% by weight, the amount of resin adhered to the ballast will be too small after drying, and the desired prevention effect will not be obtained. The average particle size of the resin emulsion is
Affects the dryness and viscosity of the resin emulsion. In general, the smaller the average particle diameter, the better the drying property, but the higher the viscosity, and the poorer the sprayability and the penetrability of the resin emulsion. Therefore, the average particle size of the resin emulsion is preferably about 10 nm to 10 μm.
【0023】この発明で使用する凝集剤水溶液の粘度
は、特に限定はされないが、10000cps以下が好
ましい。凝集剤水溶液は、通常、如雨露や散布機を用
い、バラスト上に散布する。従って、粘度が10000
cpsを超える場合は、バラスト上に均一に散布するこ
とが困難になるからである。凝集剤は、特に限定はされ
ないが、水溶性のものが好ましい。特に、硫酸アルミニ
ウム、塩化アルミニウム、ポリ塩化アルミニウム、塩化
カルシウム、次亜燐酸カルシウム、酢酸カルシウム、プ
ロピオン酸カルシウム、塩化マグネシウム、酢酸マグネ
シウム等の多価金属塩が好ましい。これらの多価金属塩
を使用すると、高濃度で低粘度の水溶液が得やすいから
である。一方、ポリアクリルアミド系、ポリメタクリル
酸エステル系、ポリアミン系等の高分子凝集剤も使用す
ることができるが、その場合は高濃度で低粘度の水溶液
が得にくいことから、やはり、多価金属塩が好ましい。The viscosity of the aqueous flocculant solution used in the present invention is not particularly limited, but is preferably 10,000 cps or less. The coagulant aqueous solution is usually sprayed on the ballast using a raindrop or a spraying machine. Therefore, the viscosity is 10,000
This is because if it exceeds cps, it will be difficult to evenly spread it on the ballast. The aggregating agent is not particularly limited, but a water-soluble one is preferable. In particular, polyvalent metal salts such as aluminum sulfate, aluminum chloride, polyaluminum chloride, calcium chloride, calcium hypophosphite, calcium acetate, calcium propionate, magnesium chloride and magnesium acetate are preferable. This is because when these polyvalent metal salts are used, an aqueous solution having a high concentration and a low viscosity can be easily obtained. On the other hand, a polyacrylamide-based, polymethacrylic acid-based, or polyamine-based polymer flocculant can also be used, but in that case, since it is difficult to obtain a high-concentration, low-viscosity aqueous solution, a polyvalent metal salt is also used. Is preferred.
【0024】[0024]
【作用】バラスト上に水性樹脂を散布した後、凝集剤水
溶液を散布するようにすると、水性樹脂表面に瞬時に皮
膜が形成される。これは、水性樹脂が凝集剤によって電
気的に中和され、凝集反応が起きるからである。この時
形成された凝集皮膜は、降雨等で溶出するものでなく、
樹脂の散布直後に降雨等があっても樹脂の流出を防ぐこ
とができ、列車の風圧によるバラスト飛散を防止できる
程度のバラスト固着強度を出すことができる。When the aqueous resin is sprayed on the ballast and then the aqueous flocculant solution is sprayed, a film is instantaneously formed on the surface of the aqueous resin. This is because the aqueous resin is electrically neutralized by the aggregating agent to cause an aggregating reaction. The agglomerated film formed at this time does not elute due to rainfall, etc.,
Even if there is rainfall or the like immediately after the resin is sprayed, the resin can be prevented from flowing out, and the ballast fixing strength can be provided to the extent that the ballast scattering due to the wind pressure of the train can be prevented.
【0025】[0025]
【実施例】以下に、この発明の実施例および比較例を示
すが、この発明は、下記実施例に限定されない。なお、
各例中、「部」および「%」は重量基準である。 −参考例1(樹脂エマルジョンの製法)− 攪拌機、還流冷却管、温度計、窒素導入管および滴下ロ
ートを取り付けた反応容器に、脱イオン水400部、
「ハイテノールN−08」(ポリオキシエチレンノニル
フェニル硫酸アンモニウム;第一工業製薬社製)1部お
よび過硫酸アンモニウム0.5部を仕込み、内温を80
°Cにした。この中に、メタクリル酸メチル160部、
アクリル酸ブチル230部、アクリル酸10部、「ハイ
テノールN−08」9部および脱イオン水185部から
なる単量体乳化液と、過硫酸アンモニウムの10%水溶
液3部と、亜硫酸水素ナトリウムの5%水溶液3部とを
3時間かけて同時に流入させた。流入終了後、さらに8
0°Cで2時間攪拌を行った。その後、冷却を行った
後、80メッシュの濾過器を通して、生成した内容物を
取り出した。このようにして不揮発分40%、粘度20
0cpsである樹脂エマルジョンを得た。EXAMPLES Examples and comparative examples of the present invention will be shown below, but the present invention is not limited to the following examples. In addition,
In each example, "part" and "%" are based on weight. -Reference Example 1 (Production Method of Resin Emulsion)-400 parts of deionized water was placed in a reaction vessel equipped with a stirrer, a reflux condenser, a thermometer, a nitrogen inlet tube and a dropping funnel.
1 part of "HITENOL N-08" (polyoxyethylene nonylphenyl ammonium sulfate; manufactured by Dai-ichi Kogyo Seiyaku Co., Ltd.) and 0.5 part of ammonium persulfate were charged, and the internal temperature was adjusted to 80.
It was set to ° C. In this, 160 parts of methyl methacrylate,
230 parts of butyl acrylate, 10 parts of acrylic acid, 9 parts of “HITENOL N-08” and 185 parts of deionized water, 3 parts of 10% ammonium persulfate aqueous solution, and 5 parts of sodium bisulfite. % Aqueous solution and 3 parts simultaneously were allowed to flow in simultaneously for 3 hours. 8 more after the inflow
The mixture was stirred at 0 ° C for 2 hours. Then, after cooling, the produced content was taken out through an 80-mesh filter. Thus, the nonvolatile content is 40% and the viscosity is 20.
A resin emulsion of 0 cps was obtained.
【0026】−参考例2(水溶性樹脂の製法)− 攪拌機、還流冷却管、温度計、窒素導入管および滴下ロ
ートを取り付けた反応容器に、イソプロピルアルコール
400部を仕込み、内温を80°Cにした。この中に、
スチレン90部、メタクリル酸メチル50部、アクリル
酸2エチルヘキシル180部、アクリル酸80部、アゾ
ビスイソブチロニトリル12部の混合液を3時間で滴下
した。滴下終了後、さらに80°Cで2時間攪拌した。
その後、冷却した後、28%アンモニア水で当量中和
し、水を加えた。このようにして不揮発分25%、粘度
100cpsである水溶性樹脂を得た。-Reference Example 2 (Manufacturing Method of Water-Soluble Resin)-400 parts of isopropyl alcohol was charged into a reaction vessel equipped with a stirrer, a reflux condenser, a thermometer, a nitrogen introducing tube and a dropping funnel, and the internal temperature was 80 ° C. I chose In this
A mixed solution of 90 parts of styrene, 50 parts of methyl methacrylate, 180 parts of 2-ethylhexyl acrylate, 80 parts of acrylic acid, and 12 parts of azobisisobutyronitrile was added dropwise over 3 hours. After the dropping was completed, the mixture was further stirred at 80 ° C. for 2 hours.
Then, after cooling, it was neutralized with 28% ammonia water in an equivalent amount, and water was added. Thus, a water-soluble resin having a nonvolatile content of 25% and a viscosity of 100 cps was obtained.
【0027】なお、上記参考例で得られた水性樹脂の不
揮発分および粘度の値は、以下の方法により測定したも
のである。不揮発分の測定 :水性樹脂約1gを重量既知のアルミニ
ウム皿に秤り取り、105°Cの熱風乾燥機で2時間乾
燥し、冷却後、重量を測定した。下記式より、不揮発分
濃度を算出した。The nonvolatile content and the viscosity value of the aqueous resin obtained in the above Reference Example are measured by the following methods. Measurement of non-volatile content : About 1 g of the aqueous resin was weighed in an aluminum dish of known weight, dried in a hot air dryer at 105 ° C for 2 hours, cooled, and then weighed. The nonvolatile content concentration was calculated from the following formula.
【0028】不揮発分濃度(%)={(乾燥後重量−ア
ルミニウム皿重量)/(水性樹脂)}×100粘度の測定 :水性樹脂の入った容器を25°Cの恒温槽
中に2時間以上放置後、ブルックフィールド型回転粘度
計(東京計器社製;BM型、回転数30回転)を用いて
測定した。Nonvolatile content concentration (%) = {(weight after drying-weight of aluminum dish) / (aqueous resin)} × 100 Measurement of viscosity : A container containing the aqueous resin is kept in a constant temperature bath at 25 ° C. for 2 hours or more. After standing, it was measured using a Brookfield type rotational viscometer (manufactured by Tokyo Keiki Co., Ltd .; BM type, rotation speed 30 rotations).
【0029】また、上記参考例で得られた水性樹脂につ
いて、以下の散布試験を行い、その結果を表1に示し
た。水性樹脂の散布試験 :如雨露に水性樹脂500gを入
れ、砂利上に散布し(散布面積1m2)、散布のしやすさ
と、砂利表面の濡れやすさを、下記に従って判定した。
ただし、使用した砂利は、30〜80g/個の重さを有
する砕石であった。Further, the following spraying test was carried out on the aqueous resin obtained in the above reference example, and the results are shown in Table 1. Dispersion test of aqueous resin: 500 g of the aqueous resin was put into a rain dew and sprayed on gravel (spraying area 1 m 2 ), and the easiness of spraying and the wettability of the gravel surface were evaluated according to the following.
However, the gravel used was crushed stone having a weight of 30 to 80 g / piece.
【0030】 ○…散布しやすく、砂利表面が均一に濡れた。 △…散布しやすいが、砂利表面の濡れ方に斑があった。 ×…散布しにくく、砂利表面の濡れ方に斑があった。 −参考例3(凝集剤水溶液の製法)− 硫酸アルミニウム(林純薬工業社製、試薬純1級)10
部をイオン交換水90部に溶かして凝集剤水溶液を得
た。◯: Easy to spread, and the gravel surface was uniformly wet. Δ: It is easy to spray, but there is unevenness in how the gravel surface gets wet. X: Difficult to spray, and unevenness was observed in the way the gravel surface was wet. -Reference Example 3 (Production Method of Aqueous Flocculant Solution) -Aluminum Sulfate (Hayashi Pure Chemical Industries, Ltd., Pure Reagent Grade 1) 10
Part was dissolved in 90 parts of ion-exchanged water to obtain a coagulant aqueous solution.
【0031】−参考例4(凝集剤水溶液の製法)− プロピオン酸カルシウム(林純薬工業社製、試薬1級)
10部をイオン交換水90部に溶かして凝集剤水溶液を
得た。上記の水性樹脂と凝集剤水溶液を用いて、以下の
実験を行った。 −実施例1− 参考例1で得られた樹脂エマルジョンを如雨露に500
g入れ、砂利上に散布(散布面積1m2 )し、1分を経
た後に、参考例3で得られた凝集剤水溶液100gを如
雨露で樹脂エマルジョン散布箇所に散布(散布面積1m
2 )した。Reference Example 4 (Preparation of Aqueous Flocculant Solution) -Calcium propionate (Hayashi Junyaku Kogyo KK, first grade reagent)
10 parts was dissolved in 90 parts ion-exchanged water to obtain an aqueous flocculant solution. The following experiment was conducted using the above-mentioned aqueous resin and aqueous flocculant solution. -Example 1-The resin emulsion obtained in Reference Example 1 was exposed to 500 g of rain and dew.
g, spray on gravel (scattering area 1 m 2 ), and after 1 minute, 100 g of the flocculant aqueous solution obtained in Reference Example 3 was sprayed on the resin emulsion spraying spot by rain and dew (scattering area 1 m 2
2 ) I did.
【0032】−実施例2− 参考例1で得られた樹脂エマルジョンを如雨露に500
g入れ、砂利上に散布(散布面積1m2 )し、1分を経
た後に、参考例4で得られた凝集剤水溶液100gを如
雨露で樹脂エマルジョン散布箇所に散布(散布面積1m
2 )した。 −比較例1− 凝集剤水溶液の散布を行わなかったほかは、実施例1と
同様にした。-Example 2-The resin emulsion obtained in Reference Example 1 was exposed to 500 g of rain and dew.
g, spray on gravel (scattering area 1 m 2 ), and after 1 minute, 100 g of the flocculant aqueous solution obtained in Reference Example 4 was sprayed on the resin emulsion spraying spot by rain and dew (scattering area 1 m 2
2 ) I did. -Comparative Example 1-A procedure was performed in the same manner as in Example 1 except that the aqueous flocculant solution was not sprayed.
【0033】−実施例3− 参考例2で得られた水溶性樹脂を如雨露に500g入
れ、砂利上に散布(散布面積1m2 )し、1分を経た後
に、参考例3で得られた凝集剤水溶液100gを如雨露
で樹脂エマルジョン散布箇所に散布(散布面積1m2 )
した。 −比較例2− 凝集剤水溶液の散布を行わなかったほかは、実施例3と
同様にした。Example 3-500 g of the water-soluble resin obtained in Reference Example 2 was placed in rain dew and sprayed on gravel (spraying area 1 m 2 ), and after 1 minute, the agglomeration obtained in Reference Example 3 Spray 100 g of the aqueous solution of the agent with rain and dew on the resin emulsion spraying area (spraying area 1 m 2 ).
did. -Comparative Example 2-A procedure similar to that of Example 3 was performed except that the aqueous flocculant solution was not sprayed.
【0034】上記実施例と比較例の各試験箇所につい
て、降雨による流出防止性と散布直後の風圧による飛散
防止性を評価したところ、表1に示すような結果を得
た。このときの評価試験方法は、下記のとおりである。降雨による流出防止性 : 凝集剤水溶液散布1分後に、イオン交換水500gを如
雨露で試験箇所に散布し、流出液の状態を観察した。The test points of the above-mentioned Examples and Comparative Examples were evaluated for runoff prevention by rain and scattering prevention by wind pressure immediately after spraying, and the results shown in Table 1 were obtained. The evaluation test method at this time is as follows. Preventing runoff due to rainfall : 1 minute after spraying the coagulant aqueous solution, 500 g of ion-exchanged water
Was sprayed on the test point in the rain dew was observed the condition of the effluent.
【0035】○…流出液は透明であった。 ×…流出液は白濁していた。散布直後の風圧による飛散防止性 :凝集剤水溶液散布1
分後に、風速50m/sの風を当て、砂利の動きを観察
した。その結果は、下記に従って評価した。O: The effluent was transparent. × ... The effluent was cloudy. Immediately after spraying, scattering prevention by wind pressure : Coagulant solution spray 1
After a minute, a wind speed of 50 m / s was applied and the movement of the gravel was observed. The results were evaluated according to the following.
【0036】○…全く動かなかった。 ×…飛散した。O: It did not move at all. X: Scattered.
【0037】[0037]
【表1】 [Table 1]
【0038】[0038]
【発明の効果】この発明にかかるバラスト固着方法によ
れば、水性樹脂を散布した上に凝集剤水溶液を散布した
後には、瞬時に皮膜が形成される。従って、乾燥前に降
雨等があっても、樹脂が流出することがないため、作業
が天候に左右されることもない。しかも、散布直後か
ら、列車の風圧によるバラスト飛散を防止できる程度の
バラスト固着強度を出すことができる。EFFECTS OF THE INVENTION According to the ballast fixing method according to the present invention, a film is instantaneously formed after the aqueous resin is sprayed and then the aqueous flocculant solution is sprayed. Therefore, even if there is rainfall or the like before drying, the resin does not flow out, so the work is not affected by the weather. In addition, immediately after spraying, it is possible to obtain the ballast fixing strength to the extent that ballast scattering due to the wind pressure of the train can be prevented.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 越野 佳孝 大阪市北区芝田2丁目4番24号 西日本 旅客鉄道株式会社内 (72)発明者 舘 宏一 大阪市北区芝田2丁目4番24号 西日本 旅客鉄道株式会社内 (72)発明者 菊田 照夫 大阪府吹田市西御旅町5番8号 株式会 社日本触媒 吹田製造所内 (72)発明者 中村 和彦 大阪府吹田市西御旅町5番8号 株式会 社日本触媒 吹田製造所内 (72)発明者 宮田 賢二 大阪府吹田市西御旅町5番8号 株式会 社日本触媒 吹田製造所内 (56)参考文献 特公 昭52−4802(JP,B2) ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Yoshitaka Koshino 2-4-24 Shibata, Kita-ku, Osaka West Japan Railway Company (72) Inventor Koichi Tate 2-4-24 Shibata, Kita-ku, Osaka West Japan Passenger Railway Co., Ltd. (72) Inventor Teruo Kikuta 5-8 Nishimitabicho, Suita City, Osaka Prefecture Nippon Shokubai Co., Ltd. in Suita Works (72) Inventor Kazuhiko Nakamura 5-8 Nishimitabicho, Suita City, Osaka Stocks Incorporated Nippon Catalyst Co., Ltd. in Suita Plant (72) Inventor Kenji Miyata 5-8 Nishimitabicho, Suita City, Osaka Stock Company In Japan Catalyst, Suita Plant (56) References Japanese Patent Publication No. 52-4802 (JP, B2)
Claims (2)
集剤水溶液を散布することを特徴とするバラスト固着方
法。1. A method for fixing ballast, which comprises spraying an aqueous resin on the ballast and then spraying an aqueous flocculant solution.
を特徴とする請求項1記載のバラスト固着方法。2. The ballast fixing method according to claim 1, wherein a polyvalent metal salt is used as the aggregating agent.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5222641A JP2544891B2 (en) | 1992-09-08 | 1993-09-07 | Ballast fixing method |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP23973792 | 1992-09-08 | ||
| JP4-239737 | 1992-09-08 | ||
| JP5222641A JP2544891B2 (en) | 1992-09-08 | 1993-09-07 | Ballast fixing method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH06158601A JPH06158601A (en) | 1994-06-07 |
| JP2544891B2 true JP2544891B2 (en) | 1996-10-16 |
Family
ID=26524985
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5222641A Expired - Fee Related JP2544891B2 (en) | 1992-09-08 | 1993-09-07 | Ballast fixing method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2544891B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3336002B1 (en) * | 2001-11-07 | 2002-10-21 | サンスター技研株式会社 | Collapse method of the fixed ballast ballast |
| JP7664199B2 (en) * | 2021-07-08 | 2025-04-17 | 公益財団法人鉄道総合技術研究所 | Ballast track repair method and repair materials, and ballast track |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS524802A (en) * | 1975-07-01 | 1977-01-14 | Matsushita Electric Ind Co Ltd | Headphones |
-
1993
- 1993-09-07 JP JP5222641A patent/JP2544891B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH06158601A (en) | 1994-06-07 |
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