JP2008274201A - Asbestos dust catcher and method for catching dust - Google Patents
Asbestos dust catcher and method for catching dust Download PDFInfo
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- JP2008274201A JP2008274201A JP2007146113A JP2007146113A JP2008274201A JP 2008274201 A JP2008274201 A JP 2008274201A JP 2007146113 A JP2007146113 A JP 2007146113A JP 2007146113 A JP2007146113 A JP 2007146113A JP 2008274201 A JP2008274201 A JP 2008274201A
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- 239000010425 asbestos Substances 0.000 title claims abstract description 60
- 229910052895 riebeckite Inorganic materials 0.000 title claims abstract description 60
- 239000000428 dust Substances 0.000 title claims abstract description 21
- 238000000034 method Methods 0.000 title claims abstract description 11
- 239000004115 Sodium Silicate Substances 0.000 claims abstract description 25
- 239000000839 emulsion Substances 0.000 claims abstract description 25
- 229910052911 sodium silicate Inorganic materials 0.000 claims abstract description 25
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims abstract description 24
- 239000004816 latex Substances 0.000 claims abstract description 12
- 229920000126 latex Polymers 0.000 claims abstract description 12
- 229920006243 acrylic copolymer Polymers 0.000 claims abstract description 10
- 238000001035 drying Methods 0.000 claims abstract description 5
- 239000000853 adhesive Substances 0.000 claims description 19
- 230000001070 adhesive effect Effects 0.000 claims description 19
- 239000007787 solid Substances 0.000 claims description 14
- 239000002516 radical scavenger Substances 0.000 claims description 12
- 238000000576 coating method Methods 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 239000011248 coating agent Substances 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 6
- 238000010276 construction Methods 0.000 claims description 6
- 238000009413 insulation Methods 0.000 claims description 6
- 239000007921 spray Substances 0.000 claims description 6
- 238000005507 spraying Methods 0.000 claims description 6
- 239000003973 paint Substances 0.000 claims description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 4
- 229910000831 Steel Inorganic materials 0.000 claims description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000004568 cement Substances 0.000 claims description 4
- 239000013521 mastic Substances 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 4
- 239000010959 steel Substances 0.000 claims description 4
- 235000010215 titanium dioxide Nutrition 0.000 claims description 4
- 229920001577 copolymer Polymers 0.000 claims description 3
- 229910052742 iron Inorganic materials 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 3
- 239000000049 pigment Substances 0.000 claims description 3
- 239000010454 slate Substances 0.000 claims description 3
- 238000003860 storage Methods 0.000 claims description 3
- 239000004111 Potassium silicate Substances 0.000 claims description 2
- 229910052913 potassium silicate Inorganic materials 0.000 claims description 2
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 claims description 2
- 235000019353 potassium silicate Nutrition 0.000 claims description 2
- 229910052910 alkali metal silicate Inorganic materials 0.000 claims 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims 1
- 229920002125 Sokalan® Polymers 0.000 claims 1
- 125000005396 acrylic acid ester group Chemical group 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 claims 1
- 239000010426 asphalt Substances 0.000 claims 1
- 239000011230 binding agent Substances 0.000 claims 1
- 238000001816 cooling Methods 0.000 claims 1
- 229910052744 lithium Inorganic materials 0.000 claims 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 claims 1
- 239000004584 polyacrylic acid Substances 0.000 claims 1
- 229910052700 potassium Inorganic materials 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- 239000002562 thickening agent Substances 0.000 claims 1
- 238000001926 trapping method Methods 0.000 claims 1
- 230000035699 permeability Effects 0.000 abstract description 7
- 239000011414 polymer cement Substances 0.000 abstract description 3
- 230000007547 defect Effects 0.000 abstract description 2
- 230000002950 deficient Effects 0.000 abstract 1
- 230000003111 delayed effect Effects 0.000 abstract 1
- 230000008595 infiltration Effects 0.000 abstract 1
- 238000001764 infiltration Methods 0.000 abstract 1
- 238000012360 testing method Methods 0.000 description 17
- 229920000742 Cotton Polymers 0.000 description 9
- 239000004744 fabric Substances 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 7
- 229920003048 styrene butadiene rubber Polymers 0.000 description 6
- 239000010410 layer Substances 0.000 description 4
- 238000011068 loading method Methods 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000010169 landfilling Methods 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- 230000008520 organization Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000000149 penetrating effect Effects 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- 239000005746 Carboxin Substances 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
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000011398 Portland cement Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000002313 adhesive film Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- GYSSRZJIHXQEHQ-UHFFFAOYSA-N carboxin Chemical compound S1CCOC(C)=C1C(=O)NC1=CC=CC=C1 GYSSRZJIHXQEHQ-UHFFFAOYSA-N 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- PVGBHEUCHKGFQP-UHFFFAOYSA-N sodium;n-[5-amino-2-(4-aminophenyl)sulfonylphenyl]sulfonylacetamide Chemical compound [Na+].CC(=O)NS(=O)(=O)C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 PVGBHEUCHKGFQP-UHFFFAOYSA-N 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
Landscapes
- Working Measures On Existing Buildindgs (AREA)
- Processing Of Solid Wastes (AREA)
Abstract
Description
本発明は建築壁面、天井または鉄骨および船舶と車輌の内壁と天井に、断熱、耐火、消音の目的で塗布したアスベスト含有塗装剤を解体除去工事中に発生するアスベスト粉塵を捕捉する。ボード表面に吹き付け含浸して乾燥させる塗装剤に関するThe present invention captures asbestos dust generated during dismantling and removal work for asbestos-containing coatings applied to architectural wall surfaces, ceilings or steel frames, and inner walls and ceilings of ships and vehicles for the purpose of heat insulation, fire resistance, and noise reduction. About coating materials that are sprayed and impregnated on the board surface to dry
従来のアスベスト解体の粉塵捕捉剤としては、特開昭63−282、161(1986)公開の珪酸ソーダを主成分とする吹付け剤と、特開平4−222、015(1992)公開のポリアクリル酸共重合エマルジョンを主成分とする吹付け剤、および特許出願No.350,558(2005)のポルトランドセメントとスチレン・ブタジェン共重合ラテックスの混合ポリマーセメント工法が公開されている。これらのアスベスト捕捉剤のうち珪酸ソーダを主成分とするものは、アスベスト含有層中に浸透性が良いが、その乾燥膜が硬脆でアスベストとの接着性が弱く、解体時にアスベストが粉塵化し易い問題点がある。またポリアクリルエマルジョンの問題点としては、その乾燥膜は強靭でアスベストとの接着性も良いが、珪酸ソーダよりキロ当たり価格が10.数倍も高く不経済である。そしてポリマーセメント法は、一般的に高粘度でアスベスト層への浸透性が充分でなく、乾燥硬化が遅い欠点がある。Conventional dust trapping agents for disassembling asbestos include spraying agents mainly composed of sodium silicate disclosed in JP-A-63-282,161 (1986), and polyacrylic disclosed in JP-A-4-222,015 (1992). A spraying agent comprising an acid copolymer emulsion as a main component and Patent Application No. 350, 558 (2005), a mixed polymer cement construction method of Portland cement and styrene / butadiene copolymer latex is disclosed. Among these asbestos scavengers, those containing sodium silicate as the main component have good permeability in the asbestos-containing layer, but the dry film is hard and brittle and has poor adhesion to asbestos, and asbestos is easily dusted during disassembly. There is a problem. The problem with polyacrylic emulsions is that the dry film is tough and has good adhesion to asbestos, but the price per kilogram of sodium silicate is 10. Several times higher and uneconomical. The polymer cement method generally has a drawback that it has a high viscosity, does not sufficiently penetrate the asbestos layer, and is slow in drying and curing.
本発明は安価で浸透性の良い珪酸ソーダを主成分とし、強靭で接着性の良いアクリルエマルジョンの混合で上記問題点の解決法を考えた。そこで各種のポリエマルジョンを珪酸ソーダと混合してみた。ポリ酢酸ビニルエマルジョン、エチレン・酢ビ(EVA)エマルジョン、各種アクリル共重合エマルジョン,SBRラテックスなどを珪酸ソーダと混合すると、珪酸ソーダと相溶性が悪く直ぐゲル化したり貯蔵中に相分離するケースがほとんどであった。そこで多くのポリマーエマルジョンの中で珪酸ソーダと相溶性の良い物をほんの2,3点見出すことが出来た。それらの製品としては、大日本インキ化学社製のアクリル共重合エマルジョン「ボンコート」14品種中LE−1043とLE520 Sの2種類と,日本ラテックス加工社のアクリル共重合エマルジョン「トマックパワー」とSBRラテックス「トマックスーパー」が珪酸ソーダと相溶性が比較的良かった。そこで安価な珪酸ソーダを主成分とその乾燥膜の硬脆とアスベストの接着性を改善するため、相溶性のよいアクリルエマルジョン、SBRラテックスの混合の浸透性と接着性について下記のような試験を行った。The present invention conceived a solution to the above problem by mixing an inexpensive and highly penetrable sodium silicate, and a strong and adhesive acrylic emulsion. Therefore, various polyemulsions were mixed with sodium silicate. Polyvinyl acetate emulsions, ethylene / vinyl acetate (EVA) emulsions, various acrylic copolymer emulsions, SBR latex, etc. are mixed with sodium silicate so that they are poorly compatible with sodium silicate and immediately gel or phase separate during storage. Met. Therefore, we were able to find only a few of many polymer emulsions that are compatible with sodium silicate. These products include two types of acrylic copolymer emulsion “Boncoat” manufactured by Dainippon Ink Chemical Co., Ltd., 14 types of LE-1043 and LE520 S, acrylic copolymer emulsion “Tomac Power” manufactured by Nippon Latex Processing Co., Ltd. and SBR Latex. “Tomac Super” was relatively compatible with sodium silicate. Therefore, in order to improve the adhesiveness of hard and brittle and asbestos of the main component and its dry film with inexpensive sodium silicate, the following tests were conducted on the permeability and adhesiveness of the mixture of highly compatible acrylic emulsion and SBR latex. It was.
珪酸ソーダ(3号、ソリッド30%)100部、ボンコートLE520S(ソリッド16%)100部、水(H2O)100部、カルボキシンメチルセルロース(CMC)1部の混合液(試験No.3、A5−2A−1)100部,H2O 100部、CMC 1部の混合液を用いた。試験供試体には木綿布(0.3mm厚、25×200mm寸法)20枚を堆積して机上に固定し、その表面に本発明混合液20gを刷毛で均等に塗布し、その刷毛で表面をしごいて圧着し24時間放置乾燥してから25mm幅に切断して剥離試験供試体とした。剥離接着強さ試験法はJISK 6854、T型はくり法とし、ストローク5mm〜95mmの範囲の剥離接着強さを測定した。その際木綿布堆積の上2枚をNo.1とし以下No.9までの接着布を用いて剥離強さを測定したデータを図−1と図−2に示す。かようにストローク5mm〜95mmの剥離強さの測定曲線の凸点最高値1330.92g、凹点最低値582.322g、凸部平均強さ993.931g、凹部平均強さ875.982g、凸凹平均強さ934.967gであった。試験片No.2〜No.9の凸凹平均強さは、それぞれ416.064g、269.094g、240.111g、217.834g、203.96g、191.998g、168.165g、137.284gとなり、実施例No.A5−2A−1の混合液は、十分な接着強さと浸透性が良好なことが判明した。A mixed liquid of 100 parts of sodium silicate (No. 3, solid 30%), 100 parts of Boncoat LE520S (solid 16%), 100 parts of water (H 2 O) and 1 part of carboxin methylcellulose (CMC) (Test No. 3, A5 -2A-1) 100 parts of H 2 O 100 parts, was used a mixture of 1 part of CMC. On the test specimen, 20 pieces of cotton cloth (0.3 mm thickness, 25 × 200 mm size) were deposited and fixed on a desk, and 20 g of the present mixed solution was evenly applied to the surface with a brush, and the surface was covered with the brush. After squeezing, pressing and drying for 24 hours, the specimen was cut to a width of 25 mm and used as a peel test specimen. The peel adhesion strength test method was JISK 6854, T-type peel method, and the peel adhesion strength in the range of 5 mm to 95 mm stroke was measured. At that time, the top two pieces of cotton cloth piled No. 1 and below. Data obtained by measuring peel strength using up to 9 adhesive cloths are shown in FIGS. Thus, the convex point maximum value 1330.92 g, the concave point minimum value 582.322 g, the convex part average strength 993.931 g, the concave part average strength 875.982 g, the concave and convex average of the measurement curve of the peel strength with a stroke of 5 mm to 95 mm. The strength was 934.967 g. Specimen No. 2-No. 9 has an uneven average strength of 416.064 g, 269.094 g, 240.111 g, 217.834 g, 203.96 g, 191.998 g, 168.165 g, and 137.284 g, respectively. It was found that the mixed solution of A 5 -2A-1 had satisfactory adhesive strength and good permeability.
アクリル酸共重合LE 520S 100部、H2O 100部,CMC 1部の混合配合試験No.3A−5Bを用い、実施例1と同様に木綿布堆積に塗布乾燥した供試体の剥離接着強さの測定値を図−3に示している。かように凸点最大値745.394、凹点最低値381.438g、凸点平均値535.366g、凹点平均値458.196g凸凹平均値496.181g、最下端No.8で凸凹平均202.123gで、十分な接着強さと浸透性も良好であった。しかし実施例1に比して若干接着強さが低く、そのキロ当たり単価が極めて高い問題点がある。Acrylic acid copolymer LE 520S 100 parts, H 2 O 100 parts, CMC 1 part mixed compounding test No. FIG. 3 shows the measured values of the peel adhesion strength of the specimens applied to and dried on the cotton cloth in the same manner as in Example 1 using 3A-5B. Thus, the convex point maximum value 745.394, the concave point minimum value 381.438 g, the convex point average value 535.366 g, the concave point average value 458.196 g, the convex and concave average value 496.181 g, the bottom end No. 8 had an average roughness of 202.123 g, and sufficient adhesive strength and permeability were good. However, the adhesive strength is slightly lower than that of Example 1, and the unit price per kilometer is extremely high.
珪酸ソーダ(ソリッド30%)100部,H2O 100部、CMC 1部の配合で上記と同様な木綿布の接着強さを測定した結果、接着膜がガラス状硬脆で、剥離試験直後に接着した木綿布が折れてしまい測定不能となった。As a result of measuring the adhesive strength of cotton cloth similar to the above with a composition of 100 parts of sodium silicate (solid 30%), 100 parts of H 2 O and 1 part of CMC, the adhesive film was glassy hard and brittle and immediately after the peel test The bonded cotton cloth broke and became impossible to measure.
図−4に示すように、珪酸ソーダ(ソリッド30%)100部、アクリルエマルジョンLE520S(ソリッド16%)100部、75部、50部、25部、15部、5部と減量し、H2O 100部、CMC 0.5部の混合配合で上記と同様に剥離接着力を測定すると凸点最大強さが738g、537g、480g,245g、125g、0gになり、凸凹平均値もそれぞれ420g、396g、166g、78g、45g、0gとなった。かように珪酸ソーダに対しアクリルエマルジョンを100部から5部に順次減量するにつれて接着強さが次つぎに減少し、No6の5部では接着強さが0になった。 As shown in Figure 4 , sodium silicate (solid 30%) 100 parts, acrylic emulsion LE520S (solid 16%) 100 parts, 75 parts, 50 parts, 25 parts, 15 parts, 5 parts, and reduced to H 2 O When the peel adhesion strength was measured in the same manner as described above with a mixture of 100 parts and 0.5 parts of CMC, the maximum strength of the convex points was 738 g, 537 g, 480 g, 245 g, 125 g, and 0 g, and the unevenness average values were 420 g and 396 g, respectively. 166 g, 78 g, 45 g, 0 g. Thus, as the acrylic emulsion was gradually reduced from 100 parts to 5 parts with respect to sodium silicate, the adhesive strength gradually decreased, and in No. 6 part 5, the adhesive strength became zero.
珪酸ソーダ(ソリッド30%)100部、アクリルエマルジョン(日本ラッテクス社トマックパワー、ソリッド45%)100部、H2O120部、CMC1.2部の混合配合を用い実施例1同様な木綿布同士の剥離接着強さを測定した結果、接着布No.1の凸点最大強さが2968gを示し、9枚目の接着強さが466gとなった。かような実施例1に比して実施例3の剥離接着強さが大幅に強いことが判明した。その理由としては前者のアクリルエマルジョンのソリッドが16%に対し、後者が45%と高いことが基因している。100 parts of sodium silicate (solid 30%), 100 parts of acrylic emulsion (Nippon Latex Tomac Power, solid 45%), 120 parts of H 2 O, and 1.2 parts of CMC are used to separate cotton cloths as in Example 1. As a result of measuring the adhesive strength, the adhesive cloth No. The maximum convex point strength of 1 was 2968 g, and the adhesive strength of the ninth sheet was 466 g. It was found that the peel adhesion strength of Example 3 was significantly stronger than that of Example 1. The reason is that the solid of the former acrylic emulsion is 16%, while the latter is as high as 45%.
珪酸ソーダ(ソリッド30%)100部、日本ラテックス加工社のSBRラテックス(トマックパワーKT 9125C、ソリッド45%)100部、H2O130部、CMC1.3部の混合配合で実施例1と同様な木綿布の接着剥離強さを測定した結果,上部1枚目の試験片の凸点最大1990g、最下側8枚目の凸点最高1133.6gとなり、極めて良好な浸透性と高い剥離接着強さを示した。次に木綿布接着試験片を3日放置してから、H2O(25℃)中に、120分浸漬した直後に剥離接着強さを測定した結果、上側1枚目の凸点最大値728.2g、下側8枚目705.7gとかなり耐水性が良好なことが判明したCotton similar to Example 1 with a mixture of 100 parts of sodium silicate (solid 30%), 100 parts of SBR latex (Tomac Power KT 9125C, solid 45%), 130 parts of H 2 O and 1.3 parts of CMC from Nippon Latex Processing Co., Ltd. As a result of measuring the adhesive peel strength of the cloth, the maximum convex point of the upper first test piece was 1990 g, and the maximum convex point of the lowermost eighth sheet was 1133.6 g. Very good permeability and high peel adhesive strength. showed that. Next, the cotton cloth adhesion test piece was allowed to stand for 3 days, and the peel adhesion strength was measured immediately after being immersed in H 2 O (25 ° C.) for 120 minutes. .2g, the lower 8th sheet 705.7g, it was found that the water resistance is quite good
アスベストマスチック吹付板(3mm厚、15×25cm寸法)の表面と裏面150gづつ均等に塗布し、室温で3日乾燥硬化した試験片を作り、下記の通りアスベストの粉塵試験を行った。
(1)試験機関:
NPO法人日本住宅機構 東京都中央区八重洲2−8−11川奈ビル
TEL 03−6241−0875
(2)粉塵中のアスベスト検出器: オリンパスBX51位相差顕微鏡
(3)試験法:
吸収袋(18lポリエチレン袋)中で、実施例3の配合液を表面に塗布乾燥したアスベスト吹付板を両手で折り壊して5〜20mm寸法の粉々にしてから袋をゴム輪で密封し、試験直前に閉じ口の袋を手に持って3回振り廻して粉塵を発生させ、粉塵を含む空気を細いパイプで吸引して顕微鏡用ガラス板上に粉塵を堆積させてから分散染色分析法によって顕微鏡(屈折率1.686、倍率40倍)で測定した写真を図5に示している。その分析結果は下記の通りである。
(i)捕捉剤塗布なしの試験版の3標本で、1000粒子中に石綿繊維がMAX、10粒子が確認された。(写真上)
(ii)捕捉剤を片面と両面に塗布した試験片では、石綿繊維が全く確認されなかった。(写真中、下)Asbestos mastic spray plates (thickness of 3 mm, 15 × 25 cm dimensions) were coated evenly on the front and back surfaces of 150 g, and test pieces were dried and cured at room temperature for 3 days, and the asbestos dust test was performed as follows.
(1) Testing organization:
NPO Japan Housing Organization 2-8-11 Kawana Building, Yaesu, Chuo-ku, Tokyo
TEL 03-6241-0875
(2) Asbestos detector in dust: Olympus BX51 phase contrast microscope (3) Test method:
In an absorbent bag (18-liter polyethylene bag), the asbestos spray plate coated with the composition of Example 3 on the surface and dried is broken with both hands to break up into pieces of 5 to 20 mm, and the bag is sealed with a rubber ring, immediately before the test. Holding the closed bag in hand and shaking it three times to generate dust, sucking the air containing dust with a thin pipe and depositing the dust on the microscope glass plate, and then using a dispersion staining analysis method to make a microscope ( A photograph measured at a refractive index of 1.686 and a magnification of 40 times is shown in FIG. The analysis results are as follows.
(I) In three specimens of the test version without application of the scavenger, asbestos fibers were found to be MAX in 10 particles, and 10 particles were confirmed. (On photo)
(Ii) Asbestos fibers were not confirmed at all in the test piece in which the scavenger was applied to one side and both sides. (In the photo, below)
従来のアスベスト含有ボードの解体工法は、手作業か機器を用いて無作別に解体剥離してきた。この工法ではボードの無作別な剥離と衝撃によって、アスベストの粉塵が100%捕捉されずに空気中に再飛散する危険性があった。本発明のアスベスト捕捉工法は、ボード中に浸透するだけでなく、ボード表面に30×(30〜120)cm角にカッターなどで基盤に達するまで切れ目を予めつけておき、ボード表面に本発明の捕捉剤を吹付けなどで塗布してボード内部に浸透させると共に、表面に強靭な膜を形成させ、解体時に左官コテなどで切断した四角形の一枚づつを入念に剥離し床上に密接して並べておき、裏面にも捕捉剤を軽くスプレー塗布し、間もなく30〜50cm高さに堆積して紐で十字に縛ってからトラックに積み上げる。かような工法は従来の無作別解体屑に比べてトラックで嵩高にならず、1台当りの荷積量と埋立量が大幅に増加して経済的で、荷積と埋立時のアスベスト粉塵の危険性が大幅に少なくなる。The conventional method of disassembling an asbestos-containing board has been dismantled and peeled randomly by hand or using equipment. In this construction method, there was a risk that asbestos dust would not be captured 100% and would re-scatter into the air due to random peeling and impact of the board. The asbestos capturing method of the present invention not only penetrates into the board, but also cuts a 30 × (30 to 120) cm square on the board surface in advance until it reaches the base with a cutter or the like. Applying the scavenger by spraying and penetrating the inside of the board, forming a tough film on the surface, carefully peeling each of the squares cut with a plastering iron etc. at the time of dismantling and arranging them closely on the floor Then, the backside is lightly sprayed with the scavenger, and it will soon be deposited to a height of 30-50 cm, tied to a cross with a string, and then stacked on a track. Such a construction method is not bulky with trucks compared to conventional unsorted demolition waste, and the amount of loading and landfill per vehicle is greatly increased, which is economical, and asbestos dust during loading and landfilling The risk of is greatly reduced.
全国の学校、体育館、工場、倉庫の壁天井に既設したアスベスト含有セメントスレート板は数えきれぬほど多数既存している。これらの解体と代替品の貼り付けには莫大な金額と手数をようする。大型船舶の内壁の断熱アスベスト含有吹き付塗装、ボイラー、溶鉱炉の本体と配管、温泉冷却器の配管被覆層にも、アスベストが含有している。これらのアスベスト含有層を解体と代替する代りに本発明のアスベスト捕捉剤にチタン白などの顔料を混合した水性塗料を表面に塗布して半永久的にアスベスト飛散を防止する工法を考案した。その塗料配合としては、珪酸カリ(30%ソリッド)25%、アクリル共重合エマルジョン(45%)10%チタン白、タルク10%炭酸カルシュム粉15%、水30%の混練り水性塗料をアスベスト含有基材にエアレススプレーで塗布乾燥する。There are countless asbestos-containing cement slate boards already installed on the walls and ceilings of schools, gymnasiums, factories and warehouses nationwide. It takes a huge amount of money and effort to disassemble and paste these alternatives. Asbestos is also contained in spray coatings containing heat-insulated asbestos on the inner walls of large ships, boilers, blast furnace main bodies and piping, and piping coating layers of hot spring coolers. Instead of disassembling these asbestos-containing layers, a method of semi-permanently preventing asbestos scattering by applying an aqueous paint prepared by mixing a pigment such as titanium white to the asbestos scavenger of the present invention was devised. The paint composition is asbestos-containing, based on kneaded water-based paint consisting of 25% potassium silicate (30% solid), 10% acrylic copolymer emulsion (45%) titanium white, 10% talc 15% calcium carbonate powder, 30% water. Apply and dry the material with airless spray.
建築の壁、天井および鉄骨のほか船舶、車輌内壁に吹付塗布したアスベスト含有マスチックボードは、学校,体育館などに広く使用されていた。最近アスベスト公害が続発している。とくに解体工事や建築老朽化によるアスベスト粉塵が重大な公害となっている。そのさいアスベスト飛散防止工法としては、珪酸ソーダを成分とする捕捉剤またはアクリル共重含エマルジョンを主成分とする捕捉剤が公知の通りである。前者の珪酸ソーダはアスベストボードに浸透性が良く安価な特徴があるが、乾燥硬化膜がガラス状硬脆でアスベストへの接着性が不足し、解体時や輸送埋立工事中に再飛散し、硬化膜の耐水性が悪く解体屑の野積、運搬中に雨水で流失する欠点があった。後者のアクリル共重含エマルジョンの乾燥膜は強靭で接着性と耐水性を備えているが、そのキロ当たりの単価が前者に比して10数倍(500円以上)で最近の石油ショックで値上がりの傾向になっている。そこで本発明は珪酸ソーダを主成分として相溶性がよいアクリル共重合エマルジョンかスチレン.ブタジェン(SBR)ラテックスを混合して両者の長短を相補なうアスベスト粉塵捕捉剤を考案し、各種の試験で好成績を得ることが出来たAsbestos-containing mastic boards sprayed on the walls of buildings, ceilings and steel as well as ships and vehicle interiors were widely used in schools and gymnasiums. Recently, asbestos pollution continues. In particular, asbestos dust from demolition work and aging of buildings is a serious pollution. As the asbestos scattering prevention method, a scavenger containing sodium silicate as a component or a scavenger containing an acrylic copolymer emulsion as a main component is known. The former, sodium silicate, has good permeability and low price on asbestos board, but the dry cured film is glassy hard and brittle and lacks adhesion to asbestos, and rescatters and hardens during dismantling and transportation landfill work. There was a defect that the water resistance of the membrane was poor and that the demolition waste was piled up and washed away by rainwater during transportation. The dry film of the latter acrylic co-emulsified emulsion is tough and has adhesion and water resistance, but its unit price per kilometer is 10 times higher than the former (500 yen or more), and the price has increased due to the recent oil shock. It has become a tendency. Therefore, the present invention is based on an acrylic copolymer emulsion or styrene having a good compatibility with sodium silicate as a main component. We have devised an asbestos dust trapping agent that mixes butadiene (SBR) latex and complements both, and has achieved good results in various tests.
従来のアスベスト含有ボードの解体工法は、手作業か機器を用いて無作別に解体剥離してきた。この工法ではボードの無作別な剥離と衝撃によって、アスベストの粉塵が100%捕捉されずに空気中に再飛散する危険性があった。本発明のアスベスト捕捉工法は、ボード中に浸透するだけでなく、ボード表面に30×(30〜120)cm角にカッターなどで基盤に達するまで切れ目を予めつけておき、ボード表面に本発明の捕捉剤を吹付けなどで塗布してボード内部に浸透させると共に、表面に強靭な膜を形成させ、解体時に左官コテなどで切断した四角形の一枚づつを入念に剥離し床上に密接して並べておき、裏面にも捕捉剤を軽くスプレー塗布し、間もなく30〜50cm高さに堆積して紐で十字に縛ってからトラックに積み上げる。かような工法は従来の無作別解体屑に比べてトラックで嵩高にならず、1台当りの荷積量と埋立量が大幅に増加して経済的で、荷積と埋立時のアスベスト粉塵の危険性が大幅に少なくなるThe conventional method of disassembling an asbestos-containing board has been dismantled and peeled randomly by hand or using equipment. In this construction method, there was a risk that asbestos dust would not be captured 100% and would re-scatter into the air due to random peeling and impact of the board. The asbestos capturing method of the present invention not only penetrates into the board, but also cuts a 30 × (30 to 120) cm square on the board surface in advance until it reaches the base with a cutter or the like. Applying the scavenger by spraying and penetrating the inside of the board, forming a tough film on the surface, carefully peeling each of the squares cut with a plastering iron etc. at the time of dismantling and arranging them closely on the floor Then, the backside is lightly sprayed with the scavenger, and it will soon be deposited to a height of 30-50 cm, tied to a cross with a string, and then stacked on a track. Such a construction method is not bulky with trucks compared to conventional unsorted demolition waste, and the amount of loading and landfill per vehicle is greatly increased, which is economical, and asbestos dust during loading and landfilling Greatly reduces the risk of
実施例7に示したように本発明捕捉剤にチタン白など顔料を混合した水性塗料を既存のアスベスト含有セメントスレート板に塗布乾燥する工法は、解体と代替品貼替せずに半永久的にアスベスト粉塵の発生を防止することが出来る。そのほか大型船舶の断熱被覆やボイラー、溶鉱炉、温泉水保存槽と配管被覆防止させる工法によって、アスベスト含有層の解体と代替工事が省略されて莫大な経済効果が期待できる。As shown in Example 7, a method of applying and drying an aqueous paint obtained by mixing a pigment such as titanium white to the scavenger of the present invention onto an existing asbestos-containing cement slate plate is semipermanently performed without disassembling and replacing the substitute product. Generation of dust can be prevented. In addition, the thermal insulation coating of large vessels, boilers, blast furnaces, hot spring water storage tanks, and methods of preventing pipe coating prevent the dismantling of the asbestos-containing layer and the replacement work, and enormous economic effects can be expected.
Claims (4)
(1)体育館などの壁と天井に付設したアスベスト含有セメントスレート板
(2)鉄鋼船舶の内壁と天井に塗装したアスベスト含有マスチック塗装
(3)ボイラー本体と配管の断熱被覆
(4)溶鉱炉の本体と配管の断熱被覆
(5)温泉水保存冷却槽と配管被覆The existing asbestos-containing building board (board) and heat insulation heat insulation coating shown below using an aqueous paint in which a pigment such as titanium white is mixed with an asbestos scavenger mixed with potassium silicate and acrylic copolymer emulsion in the alkali silicate of the present invention A method of spraying asphalt to prevent asbestos scattering semipermanently.
(1) Asbestos-containing cement slate plates attached to walls and ceilings of gymnasiums, etc. (2) Asbestos-containing mastic coating painted on the inner walls and ceilings of steel ships (3) Boiler body and piping insulation coating (4) Blast furnace body Insulation coating for piping (5) Hot spring water storage cooling tank and piping coating
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Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009035647A (en) * | 2007-08-02 | 2009-02-19 | Daiso Chemical Co Ltd | Dust scattering inhibitor and dust treating method |
| JP2012236888A (en) * | 2011-05-11 | 2012-12-06 | Eco First:Kk | Asbestos scattering preventing agent and asbestos material treatment method |
| JP2013060604A (en) * | 2012-11-30 | 2013-04-04 | Daiso Chemical Co Ltd | Dust-scattering inhibitor and dust-processing method |
| CN103305187A (en) * | 2013-06-28 | 2013-09-18 | 陕西煤业化工技术研究院有限责任公司 | Compound chemical coal dust suppressant and preparation method thereof |
| CN103694959A (en) * | 2013-12-20 | 2014-04-02 | 北京科技大学 | Ecological dust suppression technology of phosphate rock mountain road |
| CN104559931A (en) * | 2013-10-09 | 2015-04-29 | 青岛海德化工有限公司 | Dustproof composite film agent and preparation method thereof |
| CN104878712A (en) * | 2014-03-01 | 2015-09-02 | 北京科技大学 | Technique of suppressing heavy dust on transport road under extreme conditions |
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2007
- 2007-05-07 JP JP2007146113A patent/JP2008274201A/en active Pending
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009035647A (en) * | 2007-08-02 | 2009-02-19 | Daiso Chemical Co Ltd | Dust scattering inhibitor and dust treating method |
| JP2012236888A (en) * | 2011-05-11 | 2012-12-06 | Eco First:Kk | Asbestos scattering preventing agent and asbestos material treatment method |
| JP2013060604A (en) * | 2012-11-30 | 2013-04-04 | Daiso Chemical Co Ltd | Dust-scattering inhibitor and dust-processing method |
| CN103305187A (en) * | 2013-06-28 | 2013-09-18 | 陕西煤业化工技术研究院有限责任公司 | Compound chemical coal dust suppressant and preparation method thereof |
| CN103305187B (en) * | 2013-06-28 | 2015-04-22 | 陕西煤业化工技术研究院有限责任公司 | Compound chemical coal dust suppressant and preparation method thereof |
| CN104559931A (en) * | 2013-10-09 | 2015-04-29 | 青岛海德化工有限公司 | Dustproof composite film agent and preparation method thereof |
| CN103694959A (en) * | 2013-12-20 | 2014-04-02 | 北京科技大学 | Ecological dust suppression technology of phosphate rock mountain road |
| CN104878712A (en) * | 2014-03-01 | 2015-09-02 | 北京科技大学 | Technique of suppressing heavy dust on transport road under extreme conditions |
| CN104878712B (en) * | 2014-03-01 | 2017-02-15 | 北京科技大学 | Technique of suppressing heavy dust on transport road under extreme conditions |
| CN105062425A (en) * | 2015-08-27 | 2015-11-18 | 天津筑品科技有限公司 | Environment-friendly construction site dust suppressant and preparing method thereof |
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