JPH0228403A - Prevention of dust generation - Google Patents
Prevention of dust generationInfo
- Publication number
- JPH0228403A JPH0228403A JP17600088A JP17600088A JPH0228403A JP H0228403 A JPH0228403 A JP H0228403A JP 17600088 A JP17600088 A JP 17600088A JP 17600088 A JP17600088 A JP 17600088A JP H0228403 A JPH0228403 A JP H0228403A
- Authority
- JP
- Japan
- Prior art keywords
- dust
- component
- compound
- substance
- water solution
- 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.)
- Pending
Links
- 239000000428 dust Substances 0.000 title claims abstract description 45
- 230000002265 prevention Effects 0.000 title claims abstract description 17
- 239000000126 substance Substances 0.000 claims abstract description 65
- 150000001875 compounds Chemical class 0.000 claims abstract description 31
- 229920000642 polymer Polymers 0.000 claims abstract description 26
- 238000005507 spraying Methods 0.000 claims abstract description 13
- 239000007864 aqueous solution Substances 0.000 claims description 23
- 238000000034 method Methods 0.000 claims description 19
- 239000006185 dispersion Substances 0.000 claims description 14
- 125000004018 acid anhydride group Chemical group 0.000 claims description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 22
- 239000003245 coal Substances 0.000 abstract description 19
- 229920001577 copolymer Polymers 0.000 abstract description 14
- -1 vinyl compound Chemical class 0.000 abstract description 13
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract description 9
- 229920002554 vinyl polymer Polymers 0.000 abstract description 4
- 239000003795 chemical substances by application Substances 0.000 abstract description 3
- 125000004432 carbon atom Chemical group C* 0.000 abstract description 2
- 239000011203 carbon fibre reinforced carbon Substances 0.000 abstract description 2
- 150000008065 acid anhydrides Chemical class 0.000 abstract 2
- 239000003513 alkali Substances 0.000 abstract 2
- ORTFAQDWJHRMNX-UHFFFAOYSA-M oxidooxomethyl Chemical compound [O-][C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-M 0.000 abstract 2
- 239000007921 spray Substances 0.000 description 15
- 239000000047 product Substances 0.000 description 13
- 230000000694 effects Effects 0.000 description 12
- 239000000571 coke Substances 0.000 description 11
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- 239000002253 acid Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
- 229920001519 homopolymer Polymers 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 238000002485 combustion reaction Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 230000002269 spontaneous effect Effects 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 239000001569 carbon dioxide Substances 0.000 description 3
- 229910002092 carbon dioxide Inorganic materials 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- 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 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 239000004568 cement Substances 0.000 description 2
- 239000003610 charcoal Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 238000001879 gelation Methods 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 2
- 229940117841 methacrylic acid copolymer Drugs 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-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
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 230000009435 amidation Effects 0.000 description 1
- 238000007112 amidation reaction Methods 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- RZBXSLICNMYVAJ-UHFFFAOYSA-N ethenyl acetate;2-methylprop-2-enoic acid Chemical compound CC(=O)OC=C.CC(=C)C(O)=O RZBXSLICNMYVAJ-UHFFFAOYSA-N 0.000 description 1
- KRWWZDVIEFSIOT-UHFFFAOYSA-N ethenyl acetate;furan-2,5-dione Chemical compound CC(=O)OC=C.O=C1OC(=O)C=C1 KRWWZDVIEFSIOT-UHFFFAOYSA-N 0.000 description 1
- CYKDLUMZOVATFT-UHFFFAOYSA-N ethenyl acetate;prop-2-enoic acid Chemical compound OC(=O)C=C.CC(=O)OC=C CYKDLUMZOVATFT-UHFFFAOYSA-N 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 150000004675 formic acid derivatives Chemical class 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000002006 petroleum coke Substances 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Solid Fuels And Fuel-Associated Substances (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、石炭、オイルコークスをはじめとする発塵性
物質の発塵を防止する発塵防止方法に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a dust generation prevention method for preventing dust generation from dust generating substances such as coal and oil coke.
現在、各種の産業分野で利用されている固体原料は、そ
の取り扱いや輸送の問題から、種々の形態がとられてい
るが、多くの場合粉体であり、発塵性を有している。こ
のような発塵性物質は、その運搬、貯蔵の段階で粉塵が
発生し、環境汚染。BACKGROUND OF THE INVENTION Currently, solid raw materials used in various industrial fields take various forms due to handling and transportation problems, but in most cases they are powders and have dust-generating properties. These dust-producing substances generate dust during transportation and storage, polluting the environment.
労働効率の低下、輸送ロスの増加、さらには粉塵爆発な
どをひきおこすため、大きな問題となっている。This has become a major problem as it reduces labor efficiency, increases transportation losses, and even causes dust explosions.
これを防く手段として、石炭などの場合には、発塵を防
止する物質を含む水溶液や水分散液を散布する方法がと
られている。たとえば特開昭5667385号公報や特
公昭57−14719号公報に示されるような界面活性
剤と保水剤とを含む水溶液を散布する方法が知られてい
る。As a means to prevent this, in the case of coal, etc., a method is used to spray an aqueous solution or aqueous dispersion containing a substance that prevents dust generation. For example, methods of spraying an aqueous solution containing a surfactant and a water retention agent are known, as disclosed in Japanese Patent Application Laid-open No. 5667385 and Japanese Patent Publication No. 57-14719.
また、水分蒸発後も発塵を防止する目的で、特開昭57
−40595号公報に示されるようなセメントベースや
、特開昭50−40491号公報に示されるようなアス
ファルト乳剤のほか、特開昭59−.51993号公報
、特開昭59−25871号公報、特開昭48−713
83号公報、特公昭51−7637号公報、特公昭53
−38082号公報、特開昭56−133392号公報
に示されるような高分子化合物の水溶液または水分散液
を散布する方法も種々試みられている。In addition, in order to prevent dust generation even after moisture evaporates,
In addition to cement bases as shown in JP-A-40595, asphalt emulsions as shown in JP-A-50-40491, as well as JP-A-59-. 51993, JP 59-25871, JP 48-713
Publication No. 83, Special Publication No. 51-7637, Special Publication No. 1983
Various methods have also been attempted in which an aqueous solution or dispersion of a polymer compound is sprayed, as shown in Japanese Patent Application Laid-open No. 38082 and Japanese Patent Application Laid-Open No. 133392/1982.
しかしながら、これら従来公知の方法においては、発塵
防止物質を発塵性物質に対しかなり多量に用いないと、
充分な効果が発揮されないため、経済的に不利であり、
またセメントベースや金属塩を含むものでは、発塵性物
質の商品価値を低下させるという問題があった。However, in these conventionally known methods, unless the dust generation prevention substance is used in a considerably large amount relative to the dust generation substance,
It is economically disadvantageous because it does not have sufficient effect,
Furthermore, those containing cement base or metal salts have the problem of lowering the commercial value of the dust-generating substance.
本発明は、上記従来の問題に鑑み、比較的少量の発塵防
止物質の使用によって効果的に発塵を防止することがで
きる発塵防止方法を提供することを目的としている。SUMMARY OF THE INVENTION In view of the above-mentioned conventional problems, it is an object of the present invention to provide a dust generation prevention method that can effectively prevent dust generation by using a relatively small amount of dust generation prevention substance.
本発明者らは、上記の目的を達成するために鋭意検討し
た結果、発塵性物質に対し特定の高分子化合物を含む水
性液とアルカリ性物質の水溶液とを散布し、この両者を
発塵性物質の表面で反応させて増粘、ゲル化させること
により、比較的少量の上記高分子化合物およびアルカリ
性物質の使用で効果的に発塵を防止でき、しかも散布液
の乾燥後も上記効果を持続させうるちのであることを知
り、本発明を完成するに至った。As a result of intensive studies to achieve the above object, the present inventors sprayed an aqueous solution containing a specific polymer compound and an aqueous solution of an alkaline substance on dust-producing substances, and By reacting on the surface of the substance to thicken and gel, it is possible to effectively prevent dust generation using a relatively small amount of the above-mentioned polymer compound and alkaline substance, and the above-mentioned effect is maintained even after the spray liquid dries. This led to the completion of the present invention.
すなわち、本発明は、発塵性物質に、A)分子内にカル
ボキシル基または酸無水物基を有する平均分子11,0
00〜100万の高分子化合物の水溶液または水分散液
と、B)アルカリ性物質の水溶液とを、散布することを
特徴とする発塵防止方法に係るものである。That is, the present invention provides dust-producing substances with A) an average molecule of 11.0 having a carboxyl group or an acid anhydride group in the molecule;
The present invention relates to a dust generation prevention method characterized by spraying an aqueous solution or aqueous dispersion of a polymer compound having a molecular weight of 1,000 to 1,000,000 and B) an aqueous solution of an alkaline substance.
本発明のA成分における分子内にカルボキシル基または
酸無水物基を有する高分子化合物としては、分子内にカ
ルボキシル基または酸無水物基と重合性炭素−炭素二重
結合とを有する炭素数3以上の化合物(以下、これを酸
基含有化合物という)の単一重合物、またはこれと共重
合しうるビニル化合物、との共重合物、さらにこれら単
一重合物や共重合物の部分エステル化物または部分アミ
ド化物を挙げることができる。これらの中でも、エステ
ル化率またはアミド化率がそれぞれ95モル%以下とさ
れた上記の部分エステル化物または部分アミド化物が特
に好適である。The polymer compound having a carboxyl group or an acid anhydride group in the molecule in component A of the present invention includes a carbon number of 3 or more and having a carboxyl group or an acid anhydride group and a polymerizable carbon-carbon double bond in the molecule. A homopolymer of a compound (hereinafter referred to as an acid group-containing compound), or a copolymer with a vinyl compound that can be copolymerized with the same, and a partial esterification product or copolymer of these homopolymers or copolymers. Partially amidated products can be mentioned. Among these, the above-mentioned partially esterified products or partially amidated products whose esterification rate or amidation rate is 95 mol % or less are particularly preferred.
これら高分子化合物の平均分子量は、1,000〜10
0万、好ましくは2.000〜80万の範囲に設定され
ているのがよい。l、 o o o未満では水への溶解
性が強(なり、また100万を超えると水に溶解分散さ
せたときの粘性などの面で取り扱い性に劣るため、本発
明の目的を達成するうえでいずれも好ましい結果を得に
くい。The average molecular weight of these polymer compounds is 1,000 to 10
00,000, preferably in the range of 2,000 to 800,000. If the molecular weight is less than 1,000,000, the solubility in water will be strong (and if it exceeds 1,000,000, the handleability will be poor in terms of viscosity etc. when dissolved and dispersed in water. In either case, it is difficult to obtain favorable results.
上記の酸基含有化合物としては、アクリル酸、メタアク
リル酸、無水マレイン酸、イタコン酸、フマル酸などが
挙げられ、またこれらと共重合しうるビニル化合物とし
ては、エチレン、イソブチレンなどのα−オレフィン、
スチレン、酢酸ビニル、アリルアルコール、アクリルア
ミド、アクリル酸アルキルエステル、メタアクリル酸ア
ルキルエステルなどが挙げられる。ここで、後者のビニ
ル化合物の使用量は、酸基含有化合物との合計量中に占
める割合が通常95モル%以下、好適には80モル%以
下であるのがよい。Examples of the acid group-containing compounds mentioned above include acrylic acid, methacrylic acid, maleic anhydride, itaconic acid, and fumaric acid, and examples of vinyl compounds that can be copolymerized with these include α-olefins such as ethylene and isobutylene. ,
Examples include styrene, vinyl acetate, allyl alcohol, acrylamide, acrylic acid alkyl ester, methacrylic acid alkyl ester, and the like. Here, the amount of the latter vinyl compound to be used is such that its proportion in the total amount with the acid group-containing compound is usually 95 mol% or less, preferably 80 mol% or less.
これら化合物を用いた高分子化合物の代表的な例として
、ポリアクリル酸、ポリメタアクリル酸、アクリル酸−
無水マレイン酸共重合物、メタアクリル酸−無水マレイ
ン酸共重合物、エチレン−無水マレイン酸共重合物、イ
ソブチレン−無水マレイン酸共重合物、スチレン−無水
マレイン酸共重合物、酢酸ビニル−無水マレイン酸共重
合物、アリルアルコール−無水マレイン酸共重合物、酢
酸ビニル−アクリル酸共重合物、酢酸ビニル−メタアク
リル酸共重合物、アリルアルコール−アクリル酸共重合
物、アリルアルコール−メタアクリル酸共重合物および
これらの部分エステル化物または部分アミド化物を挙げ
ることができる。Typical examples of polymer compounds using these compounds include polyacrylic acid, polymethacrylic acid, and acrylic acid.
Maleic anhydride copolymer, methacrylic acid-maleic anhydride copolymer, ethylene-maleic anhydride copolymer, isobutylene-maleic anhydride copolymer, styrene-maleic anhydride copolymer, vinyl acetate-maleic anhydride Acid copolymer, allyl alcohol-maleic anhydride copolymer, vinyl acetate-acrylic acid copolymer, vinyl acetate-methacrylic acid copolymer, allyl alcohol-acrylic acid copolymer, allyl alcohol-methacrylic acid copolymer Examples include polymers and partially esterified or partially amidated products thereof.
なお、部分エステル化物とするために用いるアルコール
には、メタノール、エタノール、プロパツール、ブタノ
ール、ヘキサノール、オクタツール、2−エチルヘキサ
ノール、ノナノール、ドデカノール、トリデカノール、
テトラデカノール、ペンクデカノール、ヘキサデカノー
ル、オクタデカノール、オレイルアルコール、ベンジル
アルコール、シクロヘキサノールなどの炭素数1〜30
の脂肪酸アルコール、芳香族アルコール、脂環式アルコ
ールおよびこれらのアルキレンオキシド付加物のほか、
エチレングリコール、プロピレングリコール、トリメチ
ロールプロパン、ペンタエリスリトール、ソルビトール
、ソルビタン、シュガーなどの多価アルコール、および
これらの部分エステル化物やポリオキシアルキレン付加
物、あるいはポリオキシアルキレンアルキルフェノール
などの反応性水酸基を持った化合物がある。In addition, the alcohol used to make the partially esterified product includes methanol, ethanol, propatool, butanol, hexanol, octatool, 2-ethylhexanol, nonanol, dodecanol, tridecanol,
1 to 30 carbon atoms such as tetradecanol, pencudecanol, hexadecanol, octadecanol, oleyl alcohol, benzyl alcohol, cyclohexanol, etc.
fatty acid alcohols, aromatic alcohols, alicyclic alcohols and their alkylene oxide adducts,
Polyhydric alcohols such as ethylene glycol, propylene glycol, trimethylolpropane, pentaerythritol, sorbitol, sorbitan, sugar, etc., and their partially esterified products, polyoxyalkylene adducts, and polyoxyalkylene alkylphenols with reactive hydroxyl groups There are compounds.
また、部分アミド化物とするために用いるアミノ化合物
としては、アンモニア、メチルアミン、エチルアミン、
プロピルアミン、ブチルアミン、オクチルアミン、ドデ
シルアミンなどのモノアミンのほか、エチレンジアミン
、ジエチレントリアミンなどの多価アミンや、さらにモ
ノエタノールアミン、ジェタノールアミンなどのアルキ
ロールアミンがある。In addition, amino compounds used to form partially amidated products include ammonia, methylamine, ethylamine,
In addition to monoamines such as propylamine, butylamine, octylamine, and dodecylamine, there are polyvalent amines such as ethylenediamine and diethylenetriamine, and alkylolamines such as monoethanolamine and jetanolamine.
本発明において使用するA成分は、上記の高分子化合物
の水溶液または水分散液であり、高分子化合物の種類に
応じた任意の方法で得ることができる。たとえば、酸基
含有化合物またはこれと共重合しうるビニル化合物から
なる単量体を、水中または有機溶媒中あるいは水と有機
溶媒との混合溶媒中で、適宜の重合開始剤を用いて重合
させることにより、この重合が水中の場合で、反応生成
物としての単一重合物または共重合物が水溶性のときは
そのまま水溶液として、また水難溶性または水不溶性の
ときは界面活性剤などの分散剤を用いた水分散液として
、得ることができる。Component A used in the present invention is an aqueous solution or aqueous dispersion of the above-mentioned polymer compound, and can be obtained by any method depending on the type of polymer compound. For example, a monomer consisting of an acid group-containing compound or a vinyl compound copolymerizable with the same is polymerized in water, an organic solvent, or a mixed solvent of water and an organic solvent using an appropriate polymerization initiator. When this polymerization is carried out in water, if the homopolymer or copolymer as a reaction product is water-soluble, it can be made into an aqueous solution as it is, or if it is poorly water-soluble or water-insoluble, it can be treated with a dispersant such as a surfactant. It can be obtained as an aqueous dispersion.
一方、上記の重合を有機溶媒中あるいは水と有機溶媒と
の混合溶媒中で行ったものについては、反応後溶媒を除
去し、得られた単一重合物または共重合物が固体であれ
ば粉砕し微粉末としたうえで、水中に溶解させて水溶液
とするか、または界面活性剤などの分散剤を用いて水分
散液とすればよい。なお、この操作を行っても満足すべ
き水溶液状態あるいは水分散液状態が得られないときは
、ゲル化を起こさない程度まで、アルカリ性物質を加え
て部分中和を行うようにしてもよい。On the other hand, if the above polymerization was carried out in an organic solvent or a mixed solvent of water and organic solvent, the solvent is removed after the reaction, and if the resulting homopolymer or copolymer is solid, it is pulverized. After making it into a fine powder, it may be dissolved in water to make an aqueous solution, or it may be made into an aqueous dispersion using a dispersant such as a surfactant. Note that if a satisfactory aqueous solution or aqueous dispersion state cannot be obtained even after performing this operation, partial neutralization may be performed by adding an alkaline substance to an extent that gelation does not occur.
また、高分子化合物が部分エステル化物や部分アミド化
物であるときは、上述の如くして分子内にカルボキシル
基または酸無水物基を有する単一重合物または共重合物
を得たのち、部分エステル化または部分アミド化を行い
、その後水溶液または水分散液とするようにしてもよい
し、単量体の少なくとも1種として前記酸基含有化合物
のエステル化物またはアミド化物を用いて、これを単一
重合するか共重合させ、その後水中で部分加水分解を行
って水溶液または水分散液とするようにしてもよい。In addition, when the polymer compound is a partially esterified product or a partially amidated product, after obtaining a homopolymer or copolymer having a carboxyl group or an acid anhydride group in the molecule as described above, the partially esterified product is obtained. Alternatively, an esterified product or an amidated product of the acid group-containing compound may be used as at least one of the monomers to form a single aqueous solution or aqueous dispersion. It may be polymerized or copolymerized and then partially hydrolyzed in water to form an aqueous solution or dispersion.
本発明において使用するB成分は、種々のアルカリ性物
質の水溶液であり、強アルカリ性物質から翳アルカリ性
物質まで任意に用いることができる。たとえば水酸化カ
リウム、水酸化ナトリウム、アンモニアやメチルアミン
などの水溶性低級アミン、モノエタノールアミンなどの
アルキロールアミン、強アルカリ性物質の弱酸塩、たと
えば水酸化ナトリウムやアンモニアのギ酸塩、酢酸塩、
プロピオン酸塩、炭酸塩、炭酸水素塩などが用いられる
。Component B used in the present invention is an aqueous solution of various alkaline substances, and can be arbitrarily used from strongly alkaline substances to slightly alkaline substances. For example, potassium hydroxide, sodium hydroxide, water-soluble lower amines such as ammonia and methylamine, alkylolamines such as monoethanolamine, weak acid salts of strong alkaline substances such as formates and acetates of sodium hydroxide and ammonia,
Propionate, carbonate, hydrogen carbonate, etc. are used.
これらのアルカリ性物質は、発塵性物質の種類に応じた
最適のものを選ぶことができ、たとえば発塵性物質が石
炭、オイルコークスのような燃料の場合には、カリウム
やナトリウムなどの金属はボイラーの腐食を増大させる
おそれがあるため好ましくなく、通常はアンモニア、低
級アミン、アルキロールアミンおよびこれらの弱酸塩な
どが好適なものとして用いられる。These alkaline substances can be selected depending on the type of dust-generating substance. For example, if the dust-generating substance is a fuel such as coal or oil coke, metals such as potassium or sodium can be selected. This is not preferred because it may increase corrosion of the boiler, and ammonia, lower amines, alkylolamines, and weak acid salts thereof are usually used as suitable ones.
なお、アルカリ性物質の中でも炭酸塩や炭酸水素塩を用
いると、以下の如き利点が得られるため、特に好ましい
。すなわち、これら塩はA成分と反応して炭酸ガスを発
生するため、A、B成分の接触後発泡しつつゲル化し、
その結果発塵性物質に対する被覆効率が増大するととも
に、乾燥後は強固な発泡皮膜が形成されることになる。Note that among the alkaline substances, it is particularly preferable to use carbonate or hydrogen carbonate because the following advantages can be obtained. That is, these salts react with component A to generate carbon dioxide gas, so that after the components A and B come into contact, they foam and gel.
As a result, the coating efficiency against dust-producing substances increases, and a strong foamed film is formed after drying.
また不活性な炭酸ガスによって発塵性物質表面の酸素が
置換されるため、大量の石炭を山積みした貯炭パイルの
表面に本発明の方法を適用したとき、貯炭パイル中への
酸素の移動が効果的に阻止され、現在大きな問題となっ
ている貯炭中の自然発火を防止できるという利点が得ら
れる。In addition, since oxygen on the surface of dust-producing substances is replaced by inert carbon dioxide gas, when the method of the present invention is applied to the surface of a coal storage pile where a large amount of coal is piled up, the movement of oxygen into the coal storage pile is effective. This has the advantage of preventing spontaneous combustion during coal storage, which is currently a major problem.
本発明においては、上述の如き高分子化合物の水溶液ま
たは水分散液からなるA成分と、アルカリ性物質の水溶
液からなるB成分とを、発塵性物質に散布し、この物質
表面で上記の両成分を反応させて増粘、ゲル状させるこ
とにより、その接着力で発塵性物質、特に微小の粉体粒
子を接着せしめて微小粒子に起因した発塵を防止するこ
とを特徴としており、またこれにより上記高分子化合物
およびアルカリ性物質からなる発塵防止物質の使用量が
少量でも効果的な発塵防止を図れて、かつ散布液の取り
扱いや発塵性物質への散布が容易となるなどの利点が得
られ、結果として経済的効果を大きく高めることができ
るのである。In the present invention, component A consisting of an aqueous solution or aqueous dispersion of a polymer compound as described above and component B consisting of an aqueous solution of an alkaline substance are sprayed onto a dust-generating substance, and both of the above components are applied to the surface of the substance. By reacting to thicken and form a gel, the adhesive force can be used to adhere dust-producing substances, especially minute powder particles, and prevent dust generation caused by minute particles. This makes it possible to effectively prevent dust generation even if the amount of the dust generation prevention substance made of the above-mentioned polymer compound and alkaline substance is used, and the advantages include the ease of handling the spray liquid and the ease of spraying on dust-generating substances. As a result, the economic effect can be greatly increased.
すなわち、本発明のA成分における分子内にカルボキシ
ル基または酸無水物基を有する高分子化合物は、水中に
おける分子の状態として、分子がからみあったいわゆる
糸まり状となっているものと考えられ、そのために水溶
液にしても水分散液にしても非常に取り扱いやすい状態
となっている。That is, the polymer compound having a carboxyl group or an acid anhydride group in the molecule in the component A of the present invention is considered to have a so-called thread-like state in which the molecules are entangled in water. It is very easy to handle whether it is made into an aqueous solution or an aqueous dispersion.
この状態にB成分のアルカリ性物質を接触させると、カ
ルボキシル基および酸無水物基が中和され、アルカリ性
物質のカチオン基の反発により分子は伸びた状態となっ
て流動性を失い、極端に増粘しゲル状態に変化する。When the alkaline substance of component B is brought into contact with this state, the carboxyl groups and acid anhydride groups are neutralized, and due to the repulsion of the cationic groups of the alkaline substance, the molecules become elongated, lose fluidity, and become extremely viscous. It changes to a gel state.
ここで、散布液として最初から中和されたこのような高
分子物質を用いると、水への溶解に多大の時間を要する
ため、たとえば石炭の貯炭場に高速撹拌機を備えてかつ
加熱機構も有する専用の溶解槽を設ける必要があるし、
その製造時に水溶液ないし水分散液とする場合にも非常
に低濃度のものしかできず、上記貯炭場などの現場へ搬
入するための輸送コストを勘案すると、経済性の面から
工業化は全く不可能といってもよい。If such a polymer substance, which has been neutralized from the beginning, is used as a spray liquid, it will take a long time to dissolve in water. It is necessary to provide a dedicated dissolution tank with
Even when it is made into an aqueous solution or aqueous dispersion during production, only a very low concentration can be produced, and considering the transportation cost to bring it to the coal storage site and other sites mentioned above, industrialization is completely impossible from an economic standpoint. You can say that.
これに対し、上記の本発明の方法では、A成分は水溶液
または水分散液からなる流体としてかつ高濃度で取り扱
うことができ、一方貯炭場などの現場においては比例注
入ポンプなどで面単に水で希釈して散布することができ
るし、その散布液の濃度が低くてもアルカリ性物質との
接触によって上述のとおり増粘、ゲル化して良好な防塵
機能を発揮させることができる。つまり輸送および散布
作業共に経済的にしてかつ容易に行え、しかも防塵効果
も大きくなるのである。On the other hand, in the method of the present invention described above, component A can be handled as a fluid consisting of an aqueous solution or an aqueous dispersion at a high concentration. It can be diluted and sprayed, and even if the concentration of the spray liquid is low, it can thicken and gel as described above upon contact with an alkaline substance, and exhibits a good dustproofing function. In other words, transportation and spraying operations can be carried out economically and easily, and the dust-proofing effect is also improved.
本発明の適用の対象となる発塵性物質としては、いかな
るものでもよく、たとえば石炭、オイルコークス、鉄鉱
石、砂、土、炭酸カルシウム、酸化チタン、タルク、ア
スベストなどを挙げることができる。このうち、オイル
コークスは従来技術ではその発塵防止を図ることが困難
とされていたものであるが、本発明によれば他のものと
同様にその発塵を良好に防止できるため、本発明の適用
効果が特に大きいものといえる。The dust-generating substance to which the present invention is applied may be any substance, such as coal, oil coke, iron ore, sand, earth, calcium carbonate, titanium oxide, talc, and asbestos. Among these, it has been difficult to prevent oil coke from generating dust using conventional techniques, but according to the present invention, dust generation can be effectively prevented as well as from other types of oil coke. It can be said that the effect of application is particularly large.
本発明においてこのような発塵性物質へのA成分および
B成分の散布方法は、特に限定されるものではないが、
ひとつの方法として、A成分またはB成分のいずれか一
方を発塵性物質にスプレーガンなどで散布したのち混合
して浸透させ、その後に残りの一方を同様手段で散布し
て混合する方法がある。この方法を採用するときは、A
成分中の高分子化合物の濃度およびB成分中のアルカリ
性物質の濃度を、共に通常0.01〜90重量%、好ま
しくは0.1〜60重量%の範囲に設定して行えばよい
。In the present invention, the method of spraying component A and component B onto such dust-producing substances is not particularly limited, but
One method is to spray either component A or component B onto a dust-producing substance using a spray gun, mix and allow it to penetrate, and then spray and mix the other component using the same method. . When adopting this method, A
The concentration of the polymer compound in the component and the concentration of the alkaline substance in the component B may both be set within the range of usually 0.01 to 90% by weight, preferably 0.1 to 60% by weight.
また、他のひとつの方法として、野積みされた発塵性物
質上にA成分またはB成分のいずれか一方をスプレーガ
ンなどで散布し、その後に残りの一方を同様手段で散布
して、野積みパイル上に増粘、ゲル化した皮膜を形成し
、水分蒸発後に固結層を生じさせる方法がある。この方
法を採用するときは、A成分中の高分子化合物の濃度お
よびB成分中のアルカリ性物質の濃度を、共に通常00
O1〜90重量%、好ましくは1〜80重世%の範囲に
設定して行えばよい。また、B成分として炭酸塩または
炭酸水素塩を使用すると、既述のとおり、炭酸ガスの発
生に基づく発泡皮膜が形成されるため、被覆効率の飛躍
的な向上が図れて、自然発火なども抑制するうえ、固結
層の強度が増大するなどの利点が得られる。Another method is to spray either component A or component B with a spray gun or the like on the dust-generating materials piled up in the open, and then spray the remaining one by the same means. There is a method in which a thickened, gelled film is formed on the pile, and a solidified layer is formed after the water evaporates. When this method is adopted, the concentration of the polymer compound in component A and the concentration of the alkaline substance in component B are usually set to 0.
O may be set in a range of 1 to 90% by weight, preferably 1 to 80% by weight. In addition, when carbonate or hydrogen carbonate is used as component B, as mentioned above, a foamed film is formed based on the generation of carbon dioxide gas, which dramatically improves coating efficiency and suppresses spontaneous combustion. Moreover, advantages such as increased strength of the consolidated layer can be obtained.
これら散布において、A成分とB成分の散布量は、両成
分の固形分つまり高分子物質およびアルカリ性物質の合
計量が発塵性物質に対して5 ppm〜5重量%、好ま
しくは10ppm〜1重量%の範囲となるようにするの
がよく、過少では効果が少なく、過多では経済的に不利
となる。また、A成分に対するB成分の使用量は、A成
分中の高分子化合物に含まれるカルボキシル基または酸
無水物基を中和するに充分な量、つまり上記基に対して
中和当量ないしそれ以上のアルカリ性物質を含む量とす
ればよい。In these spraying operations, the amount of spraying of component A and component B is such that the solid content of both components, that is, the total amount of polymeric substances and alkaline substances, is 5 ppm to 5% by weight, preferably 10 ppm to 1 weight%, based on the dust-generating substance. It is preferable to keep the amount within a range of 1.5%; too little will result in little effect, and too much will be economically disadvantageous. In addition, the amount of component B to be used relative to component A is an amount sufficient to neutralize the carboxyl group or acid anhydride group contained in the polymer compound in component A, that is, a neutralization equivalent to or more than the above group. The amount may include an alkaline substance.
なお、上記の散布に際し、たとえばA、B成分の発塵性
物質への浸透を促進する目的で、非イオン性界面活性剤
、アニオン性界面活性剤などの界面活性物質をA成分ま
たはB成分に添加したり、ゲル化の促進や発泡皮膜を形
成する際の泡安定化の目的で、カルボキメチルセルロー
ス
ルアルコールのような水溶性高分子をA成分またはB成
分に添加してもよく、これにより発塵防止効果をさらに
大きくすることもできる。In addition, during the above-mentioned spraying, a surfactant such as a nonionic surfactant or anionic surfactant may be added to the A or B component for the purpose of promoting the penetration of the A and B components into the dust-generating substance. A water-soluble polymer such as carboxymethylcellulose alcohol may be added to component A or component B for the purpose of promoting gelation or stabilizing foam when forming a foamed film. It is also possible to further increase the dust prevention effect.
以上のように、本発明においては、発塵防止物質として
の特定の高分子化合物およびアルカ性物質を別々に含む
A,B成分からなる二液を散布するという簡単な手段を
採用したことにより、上記発塵防止物質の使用量が僅か
でも大きな発塵防止効果を得ることができるうえに、作
業性の面でも良好となるなど従来技術では達成不可能な
格別の効果が奏し得られるものである。As described above, in the present invention, by adopting a simple method of spraying two liquids consisting of components A and B that separately contain a specific polymer compound and an alkaline substance as a dust prevention substance, Even if the amount of the above-mentioned dust generation prevention substance used is small, a large dust generation prevention effect can be obtained, and it is also possible to achieve special effects that cannot be achieved with conventional technology, such as improved workability. .
つぎに、本発明の実施例を記載してより具体的に説明す
る。なお以下、%,部とあるは、特に断らない限り、重
量%,重量部である。Next, examples of the present invention will be described in more detail. In addition, hereinafter, % and parts mean % and parts by weight unless otherwise specified.
また、以下の実施例および比較例で用いた発塵防止物質
としてのA−1〜15 (A成分の高分子化合物)、B
−1〜8 (B成分のアルカリ性物質)およびC−1〜
4(その他の物質)は、つぎの第1. 2表に示すも
のである。In addition, A-1 to 15 (polymer compounds of component A) and B as dust prevention substances used in the following examples and comparative examples.
-1~8 (Alkaline substance of component B) and C-1~
4 (other substances) is the following 1. These are shown in Table 2.
第
表
実施例1
オーストラリア産のプレアソール炭を風乾し、全水分l
O%の原炭を用意した。これをニーグーに入れ、水およ
び第3.4表に示す薬剤(発塵防止物質)の希釈液をス
プレーしながら加え、60rpmでトータル10分間撹
拌したのち、ASTM−D547−41で示されるDu
st Box試験に供し、発塵防止効果を調べた。Table 1 Example 1 Australian Preasol charcoal was air-dried, with a total water content of 1
Raw coal of 0% was prepared. This was placed in a Nigu, water and a diluted solution of the agent (dust generation prevention substance) shown in Table 3.4 were added while spraying, and the mixture was stirred at 60 rpm for a total of 10 minutes.
It was subjected to a st Box test to examine its dust generation prevention effect.
本発明例の場合は、ますA成分をその薬剤が石炭に対し
70ppmとなるように加え、5分後にB成分をその薬
剤が石炭に対し30ppmとなるように加えてさらに5
分間撹拌し、上記試験に供した。In the case of the example of the present invention, component A is first added so that the chemical concentration is 70 ppm based on the coal, and after 5 minutes, component B is added so that the chemical concentration is 30 ppm based on the coal.
The mixture was stirred for a minute and subjected to the above test.
また比較例の場合は、その薬剤が石炭に対しlOOpp
mとなるように最初に加え10分間撹拌して、上記試験
に供した。In addition, in the case of the comparative example, the chemical was lOOpp against coal.
m and stirred for 10 minutes, then subjected to the above test.
なお、上記のDust Box試験は、一定量(22
,7kg)の石炭を高さ152.5amのBox上部か
ら落下させ、120秒後下部から61CIRの所に板を
挿入し、その板上に沈積する石炭の量をC−D−1値(
試料1 kgあたりの■)で表示するもので、本発明例
および比較例共に全水分量が13%、15%、18%の
ときのC−D−1値を測定した。この値が大きいほど発
塵量が多いことを意味する。結果は、つぎの第3.4表
に示されるとおりであった。In addition, in the above Dust Box test, a certain amount (22
, 7 kg) is dropped from the top of the Box at a height of 152.5 am, and after 120 seconds, a plate is inserted at 61 CIR from the bottom, and the amount of coal deposited on the plate is calculated by the C-D-1 value (
CD-1 values were measured when the total water content was 13%, 15%, and 18% for both the present invention example and the comparative example. The larger this value, the greater the amount of dust generated. The results were as shown in Table 3.4 below.
第
表
第
表
上記の第3,4表から明らかなように、本発明例のC−
D−1値は、比較例のものに較べ非常に小さく、発塵防
止効果がより大きいものであることがわかる。As is clear from Tables 3 and 4 above, C-
It can be seen that the D-1 value is much smaller than that of the comparative example, and the dust generation prevention effect is greater.
実施例2
平均粒径220μm、全水分2%の米国産オイルコーク
ス700gを直径20cmのシャーレに入れ、第5表に
示す本発明例の場合には、まず薬剤(高分子化合物)濃
度が1%となるように水で希釈した・A成分をオイルコ
ークスの表面積1%あたり11になるようにスプレーし
、3分後薬剤(アルカリ性物質)の0.5%希釈水溶液
からなるB成分をオイルコークスの表面積11あたり1
1になるように、スプレーした。また同表に示す比較例
の場合には、その薬剤を水で0.75%に希釈した希釈
液をオイルコークスの表面積1.(あたり21スプレー
した。Example 2 700 g of American oil coke with an average particle size of 220 μm and a total moisture content of 2% was placed in a 20 cm diameter petri dish, and in the case of the present invention example shown in Table 5, the drug (polymer compound) concentration was 1%. Spray component A diluted with water so that the ratio is 11 per 1% of the surface area of the oil coke, and after 3 minutes spray component B, which is a 0.5% diluted aqueous solution of a chemical (alkaline substance), onto the oil coke. 1 per 11 surface areas
I sprayed it so that it was 1. In addition, in the case of the comparative example shown in the same table, a diluted solution obtained by diluting the chemical with water to 0.75% was added to the surface area of oil coke. (21 sprays per area.
各シャーレを1週間室内に放置し、その後シャシを35
°に(頃け、〕゛ロロアて10m/秒の風を10分間あ
てて飛散した粉塵の重量を測定した。結果は、つぎの第
5表に示されるとおりであった。Each petri dish was left indoors for one week, then the petri dish was
The weight of the scattered dust was measured by blowing a wind of 10 m/sec for 10 minutes using a rotor.The results are shown in Table 5 below.
なお、上記の各試験例においては、石油コークス−・の
濡れ性をよくするために、薬剤有効分あたり5%量のジ
−2エチルへキシルスルホコハク酸ナトリウムを加える
ようにした。In each of the above test examples, sodium di-2-ethylhexyl sulfosuccinate was added in an amount of 5% based on the active pharmaceutical ingredient in order to improve the wettability of petroleum coke.
第
表
上記の第5表より明らがなように、本発明例では・オイ
ルコークスの表面に対しても充分な固結層を生じさせる
ことができるため、オイルコークスの発塵飛散を効果的
に防止できるものであることがわかる。Table 5 As is clear from Table 5 above, in the example of the present invention, a sufficient solidified layer can be formed on the surface of oil coke, which effectively reduces the dust scattering of oil coke. It can be seen that this can be prevented.
実施例3
中国産の大同炭を用いて、約5.0001−ンの野積み
円錐形パイルをつくり、第6表に示す本発明例の場合に
は、まず薬剤(高分子化合物)濃度が1.5%となるよ
うに水で希釈したA成分を石炭パイルの表面積IMあた
り0,71になるようにスプレーし、スプレー終了後薬
剤(アルカリ性物質)の1.5%水溶液からなるB成分
を石炭パイルの表面積1耐あたり0.31スプレーした
。また、同表に示す比較例の場合には、薬剤を水で1.
5%に希釈した希釈液を石炭パイルの表面積IMあたり
11スプレーした。その後、円錐パイルの中心部に熱転
対をさし込み、3ケ月間の温度の変化を1ケ月毎に測定
した。結果は第6表に示されるとおりであった。Example 3 Using Datong charcoal from China, an open conical pile of approximately 5.0001-ton was made, and in the case of the present invention example shown in Table 6, the drug (polymer compound) concentration was Component A diluted with water to a concentration of 0.5% is sprayed to a concentration of 0.71 per surface area IM of the coal pile, and after the spraying is finished, component B consisting of a 1.5% aqueous solution of a chemical (alkaline substance) is sprayed onto the coal. 0.31 sprays were applied per pile surface area. In addition, in the case of the comparative example shown in the same table, the drug was mixed with water for 1.
The diluent diluted to 5% was sprayed 11 times per surface area IM of the coal pile. Thereafter, a thermometer was inserted into the center of the conical pile, and changes in temperature were measured every month for three months. The results were as shown in Table 6.
第
表
注)*は200℃以上であり、自然発火が起こったこと
を示す。Table Note: * indicates a temperature of 200°C or higher, indicating that spontaneous combustion occurred.
上記の第6表から明らかなように、本発明例の場合には
、石炭の自動酸化による温度上昇を効果的に防止できた
のに対し、比較例では温度上昇が顕著となり、自然発火
に至った。As is clear from Table 6 above, in the case of the inventive example, the temperature rise due to automatic oxidation of the coal was effectively prevented, whereas in the comparative example, the temperature rise was significant, leading to spontaneous combustion. Ta.
Claims (1)
は酸無水物基を有する平均分子量1,000〜100万
の高分子化合物の水溶液または水分散液と、B)アルカ
リ性物質の水溶液とを、散布することを特徴とする発塵
防止方法。(1) For the dust-generating substance, A) an aqueous solution or aqueous dispersion of a polymer compound having an average molecular weight of 1,000 to 1,000,000 and having a carboxyl group or an acid anhydride group in the molecule, and B) an aqueous solution of an alkaline substance. A dust generation prevention method characterized by spraying.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17600088A JPH0228403A (en) | 1988-07-14 | 1988-07-14 | Prevention of dust generation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17600088A JPH0228403A (en) | 1988-07-14 | 1988-07-14 | Prevention of dust generation |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0228403A true JPH0228403A (en) | 1990-01-30 |
Family
ID=16005958
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP17600088A Pending JPH0228403A (en) | 1988-07-14 | 1988-07-14 | Prevention of dust generation |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0228403A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007145992A (en) * | 2005-11-28 | 2007-06-14 | Nikko Kagaku Kenkyusho:Kk | Dust scattering prevention agent, dust scattering prevention method using the same and method for releasing, removing and treating inorganic fiber-containing building material |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5413481A (en) * | 1977-07-02 | 1979-01-31 | Mitsui Petrochem Ind Ltd | Powder scattering inhibitor |
-
1988
- 1988-07-14 JP JP17600088A patent/JPH0228403A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5413481A (en) * | 1977-07-02 | 1979-01-31 | Mitsui Petrochem Ind Ltd | Powder scattering inhibitor |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007145992A (en) * | 2005-11-28 | 2007-06-14 | Nikko Kagaku Kenkyusho:Kk | Dust scattering prevention agent, dust scattering prevention method using the same and method for releasing, removing and treating inorganic fiber-containing building material |
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