JPH02214584A - Method for preventing scattering of asbestos dust and dust treating agent - Google Patents
Method for preventing scattering of asbestos dust and dust treating agentInfo
- Publication number
- JPH02214584A JPH02214584A JP1033646A JP3364689A JPH02214584A JP H02214584 A JPH02214584 A JP H02214584A JP 1033646 A JP1033646 A JP 1033646A JP 3364689 A JP3364689 A JP 3364689A JP H02214584 A JPH02214584 A JP H02214584A
- Authority
- JP
- Japan
- Prior art keywords
- asbestos
- dust
- scattering
- soln
- konjac
- 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
- 239000010425 asbestos Substances 0.000 title claims abstract description 61
- 229910052895 riebeckite Inorganic materials 0.000 title claims abstract description 61
- 239000000428 dust Substances 0.000 title claims abstract description 30
- 239000003795 chemical substances by application Substances 0.000 title claims description 16
- 238000000034 method Methods 0.000 title claims description 16
- 229920002752 Konjac Polymers 0.000 claims abstract description 19
- 235000010485 konjac Nutrition 0.000 claims abstract description 19
- 238000005507 spraying Methods 0.000 claims abstract description 15
- 239000000843 powder Substances 0.000 claims abstract description 14
- 230000001681 protective effect Effects 0.000 claims abstract description 7
- 239000004094 surface-active agent Substances 0.000 claims abstract description 7
- 239000000084 colloidal system Substances 0.000 claims abstract description 6
- 241001312219 Amorphophallus konjac Species 0.000 claims description 16
- 235000001206 Amorphophallus rivieri Nutrition 0.000 claims description 16
- 239000000252 konjac Substances 0.000 claims description 16
- 239000007864 aqueous solution Substances 0.000 claims description 12
- 238000009418 renovation Methods 0.000 claims description 9
- 239000003755 preservative agent Substances 0.000 claims description 4
- 230000002335 preservative effect Effects 0.000 claims description 3
- 239000012752 auxiliary agent Substances 0.000 claims 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract description 4
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 abstract description 2
- 239000005711 Benzoic acid Substances 0.000 abstract description 2
- 235000010233 benzoic acid Nutrition 0.000 abstract description 2
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 abstract description 2
- 239000000661 sodium alginate Substances 0.000 abstract description 2
- 235000010413 sodium alginate Nutrition 0.000 abstract description 2
- 229940005550 sodium alginate Drugs 0.000 abstract description 2
- 230000002421 anti-septic effect Effects 0.000 abstract 1
- RNFNDJAIBTYOQL-UHFFFAOYSA-N chloral hydrate Chemical compound OC(O)C(Cl)(Cl)Cl RNFNDJAIBTYOQL-UHFFFAOYSA-N 0.000 abstract 1
- 229960002327 chloral hydrate Drugs 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 239000000243 solution Substances 0.000 description 13
- 229940025902 konjac mannan Drugs 0.000 description 9
- 239000004568 cement Substances 0.000 description 8
- 229920000057 Mannan Polymers 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 235000013312 flour Nutrition 0.000 description 5
- 239000003973 paint Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 230000002378 acidificating effect Effects 0.000 description 4
- 239000004566 building material Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 230000002265 prevention Effects 0.000 description 4
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 3
- 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 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 238000005345 coagulation Methods 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 239000008103 glucose Substances 0.000 description 3
- 238000007711 solidification Methods 0.000 description 3
- 230000008023 solidification Effects 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- -1 alkylbenzene sulfonates Chemical class 0.000 description 2
- 239000000701 coagulant Substances 0.000 description 2
- 230000015271 coagulation Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000002075 main ingredient Substances 0.000 description 2
- 230000000149 penetrating effect Effects 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- LUEWUZLMQUOBSB-FSKGGBMCSA-N (2s,3s,4s,5s,6r)-2-[(2r,3s,4r,5r,6s)-6-[(2r,3s,4r,5s,6s)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2r,4r,5s,6r)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound O[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@H](O[C@@H](OC3[C@H](O[C@@H](O)[C@@H](O)[C@H]3O)CO)[C@@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O LUEWUZLMQUOBSB-FSKGGBMCSA-N 0.000 description 1
- QNMKGMUGYVWVFQ-UHFFFAOYSA-N 2alpha-Hydroxyursolic acid Natural products CC12CC(O)C(O)C(C)(C)C1CCC1(C)C2CC=C2C3C(C)C(C)(C)CCC3(C(O)=O)CCC21C QNMKGMUGYVWVFQ-UHFFFAOYSA-N 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
- 241000206575 Chondrus crispus Species 0.000 description 1
- 229920002581 Glucomannan Polymers 0.000 description 1
- 208000019693 Lung disease Diseases 0.000 description 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000003945 anionic surfactant Substances 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
- 239000011230 binding agent Substances 0.000 description 1
- 239000006172 buffering agent Substances 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000004567 concrete Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- HFGSQOYIOKBQOW-ZSDYHTTISA-N corosolic acid Chemical compound C1[C@@H](O)[C@H](O)C(C)(C)[C@@H]2CC[C@@]3(C)[C@]4(C)CC[C@@]5(C(O)=O)CC[C@@H](C)[C@H](C)[C@H]5C4=CC[C@@H]3[C@]21C HFGSQOYIOKBQOW-ZSDYHTTISA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
- 238000007667 floating Methods 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000007306 functionalization reaction Methods 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 229940046240 glucomannan Drugs 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 201000005202 lung cancer Diseases 0.000 description 1
- 208000020816 lung neoplasm Diseases 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 208000006178 malignant mesothelioma Diseases 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 229940023144 sodium glycolate Drugs 0.000 description 1
- 235000019830 sodium polyphosphate Nutrition 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- HFFLGKNGCAIQMO-UHFFFAOYSA-N trichloroacetaldehyde Chemical compound ClC(Cl)(Cl)C=O HFFLGKNGCAIQMO-UHFFFAOYSA-N 0.000 description 1
- JEJAMASKDTUEBZ-UHFFFAOYSA-N tris(1,1,3-tribromo-2,2-dimethylpropyl) phosphate Chemical compound BrCC(C)(C)C(Br)(Br)OP(=O)(OC(Br)(Br)C(C)(C)CBr)OC(Br)(Br)C(C)(C)CBr JEJAMASKDTUEBZ-UHFFFAOYSA-N 0.000 description 1
Landscapes
- On-Site Construction Work That Accompanies The Preparation And Application Of Concrete (AREA)
- Processing Of Solid Wastes (AREA)
- Aftertreatments Of Artificial And Natural Stones (AREA)
Abstract
Description
【発明の詳細な説明】
3、〔産業上の利用分野〕
本発明はアスベスト含有建造物等の解体、改修時に発生
する粉塵の飛散防止方法並びにその処理剤に関する。DETAILED DESCRIPTION OF THE INVENTION 3. [Industrial Application Field] The present invention relates to a method for preventing scattering of dust generated during demolition or renovation of asbestos-containing buildings, and a treatment agent therefor.
アスベスト(石綿)は耐熱性、耐薬品性、耐候性、防音
性などの優れた性質と安価なことからその多くは、ビル
等の建造物の吹き付けや内装材、天井材、床材、耐火被
覆材等に幅広く使用されている。とくに吹付はアスベス
トは吸音、断熱、結露防止、耐火などの性能に優れてい
ることからその用途もひろく、学校、病院、オフィスビ
ル、ホテル、公会堂、図書館、劇場、電話局、ポーリン
グ場などの吸音や鉄骨の耐火被覆などに用いられていた
。このように多くのアスベスト製品が使用されている社
会環境にあって、アスベストの微細な針状繊維がアスベ
スト肺に代表される肺ガン、悪性中皮腫の原因と認識さ
れ世界的にも有害性に対する危険意識が高まっている。Because asbestos has excellent properties such as heat resistance, chemical resistance, weather resistance, and soundproofing properties, and is inexpensive, it is often used for spraying, interior materials, ceiling materials, flooring materials, and fireproof coatings for buildings and other structures. Widely used for materials etc. Especially when spraying, asbestos has a wide range of applications due to its excellent properties such as sound absorption, heat insulation, dew condensation prevention, and fire resistance. It was used as a fireproof coating for steel frames. In a social environment where many asbestos products are used, the fine needle-like fibers of asbestos are recognized as the cause of lung cancer, typified by asbestos lung disease, and malignant mesothelioma, and are considered to be harmful worldwide. There is a growing awareness of the dangers of
国内でも、昭和30年以降50年までの間に施工された
アスベスト吹き付けや含有建材が多量に使用されている
建築物の解体工事が始まってそれにともなうアスベスト
粉塵の飛散防止が重要な問題となってきている。In Japan, as demolition work has begun on buildings that were constructed between 1955 and 1955 and used a large amount of asbestos-sprayed or asbestos-containing building materials, prevention of asbestos dust dispersion has become an important issue. ing.
現在問題化されているアスベストの主要存在場所は学校
に代表される建造物であり、アスベストの耐熱性、防音
効果等の特性を活かして、壁、天井等、吹き付は外装材
として使用されており、吹き付は時のバインド材として
使用されているセメントの経年劣化とともに、徐々にア
スベストが剥離、飛散しているのが現状である。The main places where asbestos is presently a problem are buildings such as schools, and asbestos is used as an exterior material for walls, ceilings, etc., taking advantage of its properties such as heat resistance and soundproofing. The current situation is that asbestos gradually peels off and scatters as the cement used as a binder deteriorates over time.
吹付はアスベスト粉塵飛散の防止は、解体又は改修工事
による除去、ならびに改修の際のカバーリングあるいは
封じ込め等によって行われている。しかし、我が国では
未だ粉塵飛散防止の処理剤、および防止工法の基準はな
い。Preventing the scattering of asbestos dust is done by removing it during demolition or renovation work, and by covering or containing it during renovations. However, in Japan, there are still no standards for treatment agents or methods for preventing dust scattering.
粉塵飛散防止対策として通常とられている水の噴霧は簡
便であるがアスベストの水による“濡れ”の悪さもあっ
て内部まで浸透し難く、かつ−旦乾燥すると効果が失わ
れてアスベストの再飛散が生じる。Spraying water, which is commonly used as a measure to prevent dust scattering, is simple, but because asbestos is poorly “wetted” by water, it is difficult to penetrate inside, and once it dries, it loses its effectiveness and can cause asbestos to scatter again. occurs.
このような現状における対策として、封じ込めについて
は内部浸透固化及び/又は表面固化等の手段がとられて
おり、アスベスト処理剤もこのような使用状況に併せて
開発されており、そのほとんどが建材中のアスベストに
よく馴染むことを目的に添加されている界面活性剤と作
業者の安全を考慮した水性塗料との組み合わせである。As countermeasures against this current situation, measures such as internal penetration solidification and/or surface solidification are being taken for containment, and asbestos treatment agents have also been developed in line with this usage situation, and most of them contain asbestos in building materials. This is a combination of a surfactant that is added to blend well with asbestos, and a water-based paint that takes worker safety into consideration.
水性塗料の主成分は、油性塗料と変わらない樹脂成分で
あり水にも溶けるように末端に水に馴染みやすい官能基
を導入したものである。このような構造をしているため
に、水性塗料の噴霧によって発生する微細な霧は、比較
的容易に従来の樹脂と同様な乾燥状態に入ってしまい霧
吹きによって、新たに発生するアスベスト粉塵を空気中
で捕捉除去するには充分でない。また表面固化した水性
塗料は剥取り、運搬、最終処分の過程で新たな粉塵を発
生し、二次公害の原因となる。The main component of water-based paints is a resin component similar to that of oil-based paints, and a functional group that is easily compatible with water has been introduced at the end so that it can be dissolved in water. Because of this structure, the fine mist generated by spraying water-based paint can relatively easily enter a dry state similar to that of conventional resin. It is not enough to trap and remove it inside. In addition, water-based paint that has solidified on the surface generates new dust during the process of peeling off, transporting, and final disposal, causing secondary pollution.
解体、改修作業時を含め、この空気中に浮遊する粉塵の
除去こそこれからの粉塵対策の目指すところである。The goal of future dust countermeasures is to remove dust floating in the air, including during demolition and renovation work.
昭和50年以降アスベスト吹き付けは、禁止されている
が、近年建造物の老朽化に伴ない使途変更、機能性化が
促進され、今後数年の間に集中すると考えられる、建造
物の解体、改修の際にアスベスト粉塵の発生、飛散が起
こり得ることが充分予測できる。Asbestos spraying has been prohibited since 1975, but in recent years as buildings have aged, changes in use and functionalization have been promoted, and demolition and renovation of buildings is expected to increase in the coming years. It can be fully predicted that asbestos dust will be generated and dispersed during this process.
よって本発明は上記建造物の解体、改修により発生する
アスベスト粉塵の飛散を防止し、かつ解体、改修に従事
する作業員の無害安全策、使用薬剤の公害汚染対策、一
般環境汚染さらには処理薬剤のコストなどの総合的見地
からみて適切且つ実用的なアスベストの粉塵飛散防止方
法並びにその処理剤を提供するものである。Therefore, the present invention is intended to prevent the scattering of asbestos dust generated by the demolition and renovation of the above-mentioned buildings, to provide non-hazardous safety measures for workers engaged in demolition and renovation, to prevent pollution from using chemicals, to prevent general environmental pollution, and to treat chemicals. The purpose of the present invention is to provide a method for preventing asbestos dust scattering that is appropriate and practical from a comprehensive standpoint such as cost, and a treatment agent for the same.
本発明はアスベストを含有する建造物の解体、改修並び
に発生する粉塵の飛散を防止せしめる方法に於いて、こ
んにゃく精粉もしくはその誘導体水溶液を噴霧すること
により表面での被膜形成を生じさせる粉塵の飛散防止方
法によって達成される。The present invention is a method for dismantling or renovating buildings containing asbestos and preventing the scattering of generated dust by spraying an aqueous solution of fine konjac powder or its derivatives to form a film on the surface of the building. This is achieved through prevention methods.
本発明に使用されるこんにゃく精粉は、たとえば本出願
人等がすでに開示した地盤の凝固方法(特公昭56−第
21780号)中の如くグルコマンナンあるいはこんに
ゃくマンナンとも呼ばれているものであり、グルコース
(Call+zOi) とマンノース(C&H1□06
)との複雑なポリ複合体であって、これを加水分解する
と2分子のマンノースと1分子のグルコースが得られる
。The konjac powder used in the present invention is also called glucomannan or konjac mannan, as described in the ground solidification method (Japanese Patent Publication No. 56-21780) already disclosed by the present applicant. Glucose (Call+zOi) and Mannose (C&H1□06
), which when hydrolyzed yields two molecules of mannose and one molecule of glucose.
即ち、こんにゃくマンナンは分子内に一箇以上(多くは
数箇)のアルコール基(OH)と−箇のアルデヒド基(
C)To)又はケトン基(CO)を有するグルコースと
マンノースのポリ縮合物である。このこんにゃくマンナ
ン(R−OHで示す)を泡水クロラールの20%溶液で
前処理した後モノクロル酢酸を使用して次式:
%式%
の様にエーテル化により、こんにゃくマンナン誘導体を
製造し、之を本発明の方法に用いる処理剤とすることが
できる。In other words, konjac mannan has one or more (often several) alcohol groups (OH) and - aldehyde groups (
C) To) or a polycondensate of glucose and mannose having a ketone group (CO). This konjac mannan (indicated by R-OH) was pretreated with a 20% solution of bubble water chloral, and then etherified using monochloroacetic acid as shown in the following formula: % formula % to produce a konjac mannan derivative. can be used as a processing agent in the method of the present invention.
吹付はアスベストの経年劣化に供なって、アスベスト繊
維が表面に突出した状態にあるとき、風圧、振動、若し
くは建造物の解体取壊し、破砕の際、大量の粉塵が発生
する状態にある。Spraying occurs when asbestos fibers protrude from the surface as the asbestos deteriorates over time, and a large amount of dust is generated during wind pressure, vibration, or when buildings are dismantled, demolished, or crushed.
本発明の方法において、このような建築物に対して0.
2〜2χ前後のこんにゃく精粉等の水溶液からなる弱酸
性を示す処理剤を噴霧すると、この処理剤がたとえば建
築主材であるセメント等のアルカリ成分と穏やかな中和
反応を起こしながら建築物表面の吹付アスベスト層に浸
透してゲル化し、また連続的な水溶液の供給がない場合
も周囲のセメント内部の塩分(主にカルシウム塩)と反
応し、表面にも凝固による安定な被膜を形成する。この
こんにゃく精粉の水溶液はアルカリ凝固剤等の添加によ
りゲル化することが知られている。In the method of the present invention, 0.
When spraying a slightly acidic treatment agent made of an aqueous solution of powdered konjac powder with a concentration of around 2 to 2χ, this treatment agent causes a mild neutralization reaction with the alkaline components of cement, the main building material, and damages the surface of the building. It penetrates the sprayed asbestos layer and turns into a gel, and even if there is no continuous supply of aqueous solution, it reacts with the salts (mainly calcium salts) inside the surrounding cement, forming a stable coating on the surface by coagulation. It is known that this aqueous solution of fine konjac powder turns into a gel by adding an alkaline coagulant or the like.
こ\で本願発明においては処理対象とするアスベスト吹
付は材等がアルカリ性を示すため場合によっては処理剤
の調製時に特にか\る凝固剤を加える必要がな(、むし
ろ酸もしくは緩衝剤を加えてpHを所定の弱酸性域に調
節しておくことも好ましい結果に至る。Therefore, in the present invention, since the asbestos material to be treated is alkaline, in some cases it is not necessary to add a coagulant when preparing the treatment agent (rather, it is not necessary to add an acid or a buffering agent). Preferable results can also be achieved by adjusting the pH to a predetermined weakly acidic range.
またこのこんにゃく精粉の水溶液はアスベストに対して
良好な“濡れ”を示すため、浸透凝固が効果的に生じ、
ゲル化後乾燥条件下にあっても、こんにゃく精粉溶液は
良好な保水性を保ち、水分が乾燥してもアスベスト繊維
がこんにゃくマンナンに安定に捕捉されて固定され飛散
を生じることはない。In addition, this aqueous solution of konjac powder shows good "wetness" to asbestos, so penetrating coagulation occurs effectively.
Even under dry conditions after gelation, the konjac powder solution maintains good water retention, and even when the water dries, the asbestos fibers are stably captured and fixed in the konjac mannan and do not scatter.
このようにこんにゃく精粉のアスベストに対する“濡れ
”したがって吸収率が良好なため、水溶液中の濃度は0
.2χ〜2χ前後でも優れた飛散防止効果を生じ、場合
によっては0.4χ〜0.7χ前後の範囲の濃度も効果
的である。In this way, konjac flour has a good "wetness" to asbestos and therefore has a good absorption rate, so the concentration in the aqueous solution is 0.
.. An excellent anti-scattering effect can be obtained even when the concentration is around 2χ to 2χ, and in some cases, a concentration in the range of around 0.4χ to 0.7χ is also effective.
本発明において使用するこんにゃく精粉又はその誘導体
に適量の保護コロイド剤を加えることも、勿論本発明に
含まれる。保護コロイド剤としては前記本出願人らの特
許に開示されているように、例えば繊維素グリコール酸
ナトリウム(C5M、S)でんぷんグリコール酸ナトリ
ウJ、(C0M、S) 、メチルセルローズ、メチルデ
ンプン、グルコノデルタラクトン(C:、 D。Of course, the present invention also includes adding an appropriate amount of a protective colloid to the konjac flour or its derivative used in the present invention. Examples of protective colloid agents include cellulose sodium glycolate (C5M,S), starch sodium glycolate J, (C0M,S), methyl cellulose, methyl starch, glucosol, as disclosed in the above-mentioned patent of the present applicants. Nodeltalactone (C:, D.
L、)カラーゲン、ポリ燐酸ナトリウム、アルギン酸ナ
トリウム等が好適でその一種またはそれ以上を混合して
使用する。その添加量は製品に対して0.1%〜lO%
特に0.3χ〜1.5χの範囲である。これらの保護コ
ロイド剤は、その優れた保護コロイド性被膜形成性、安
定性、粘性等によってこんにゃく精粉、又はその誘導体
と珪酸ナトリウム系薬液、セメント懸濁液とのコロイド
状またはゲル状組成を良好にし両者の均質な共凝固を可
能としそれによって安定性保形性のよいゲル化物を形成
せしめるものである。L.) Carrageen, sodium polyphosphate, sodium alginate, etc. are suitable, and one or more of them are used in combination. The amount added is 0.1% to 10% of the product.
In particular, it is in the range of 0.3χ to 1.5χ. These protective colloid agents have excellent protective colloidal film-forming properties, stability, viscosity, etc., and can improve the colloidal or gel-like composition of konjac flour or its derivatives, sodium silicate-based chemicals, and cement suspensions. This enables homogeneous co-coagulation of the two, thereby forming a gelled product with good stability and shape retention.
防腐剤は本処理剤である有機こんにゃく精粉の変質腐敗
を防止する上で有効であり、たとえば安息香酸およびそ
のナトリウム塩、ソルビン酸およびそのカリウム塩、パ
ラオキシ安息香酸、プロピオン酸カルシウムまたはナト
リウム塩等からなる群より選ばれる公知の防腐剤が主剤
としてのこんにゃくマンナンに対して好ましくは0.3
χ〜1.5χの範囲で添加される。Preservatives are effective in preventing deterioration and spoilage of organic konjac powder, which is the processing agent, and include benzoic acid and its sodium salt, sorbic acid and its potassium salt, paraoxybenzoic acid, propionate calcium or sodium salt, etc. A known preservative selected from the group consisting of preferably 0.3 to konjac mannan as the main ingredient.
It is added in a range of χ to 1.5χ.
界面活性剤はその浸透作用、粉塵飛散防止のために従来
からも用いられており、本発明においてもたとえばアル
キルベンゼンスルホネート系(ABS)に代表される陰
イオン系およびアルキルアリルエーテル系に代表される
非イオン系の界面活性剤を主剤としてのこんにゃくマン
ナンに対して0.3〜1.5χの範囲で併用することが
できる。尚本明細書において建材の主成分として記載さ
れているセメントはいわゆるセメントそれ自体の他適宜
骨材と混合して塗工打設された状態のものをも含む。ま
た本発明の方法はアスベスト粉塵の飛散防止に極めて有
効であるが、こんにゃく精粉水溶液のゲル化によって捕
集の可能なその他の粉塵の飛散防止にも同様に適用する
ことができる。以下本発明を実施例によってさらに説明
する。Surfactants have been conventionally used for their penetrating action and prevention of dust scattering, and in the present invention, surfactants are also used in the present invention, such as anionic surfactants such as alkylbenzene sulfonates (ABS) and non-ionic surfactants such as alkyl allyl ethers. An ionic surfactant can be used in combination with konjac mannan as the main ingredient in an amount of 0.3 to 1.5χ. In this specification, the cement described as the main component of the building material includes not only the so-called cement itself but also the cement mixed with an appropriate aggregate and applied by coating. Furthermore, although the method of the present invention is extremely effective in preventing the scattering of asbestos dust, it can be similarly applied to preventing the scattering of other dusts that can be collected by gelling an aqueous solution of fine konjac powder. The present invention will be further explained below with reference to Examples.
実施例 1
こんにゃく精粉5gをとって、1,000 ccの水道
水に添加しゆっくり撹拌して2時間放置した。溶液のp
H値は6.50と弱酸性であり、このように使用される
マンナン溶液が弱酸性を示すことは、アスベスト吹き付
は材が、セメント(アルカリ)であることを考慮すれば
望ましい要件である。Example 1 5 g of konjac flour was added to 1,000 cc of tap water, slowly stirred, and left for 2 hours. p of solution
The H value is 6.50, which is weakly acidic, and it is a desirable requirement that the mannan solution used be weakly acidic, considering that the material used for asbestos spraying is cement (alkali). .
アスベスト(試薬)をシャーレ(直径9c+w)に広げ
、400rの容器沖に置き内部ファンにより気流を起こ
し、2時間アスベスト濃度が安定するのを待って、この
時の濃度を初期濃度とした。Asbestos (reagent) was spread in a petri dish (diameter 9c+w), placed in a 400r vessel offshore to generate airflow with an internal fan, waited for the asbestos concentration to stabilize for 2 hours, and the concentration at this time was taken as the initial concentration.
400 fの容器中に前記のように調整した0、5%マ
ンナン溶液を35cc噴霧し、1時間、48時間経過後
のアスベスト粉塵を夫々採取して位相差光学顕微鏡を用
いて測定した。下記に示すように優れた結果が得られそ
の効果は現在のところアスベスト処理剤として最適なも
のとして知られているサービフレンクス(仏、セルビー
社製品の商標名)と同等もしくはそれを上回るものであ
った。35 cc of the 0.5% mannan solution prepared as described above was sprayed into a 400 F container, and asbestos dust was collected after 1 and 48 hours and measured using a phase contrast optical microscope. As shown below, excellent results have been obtained, and its effectiveness is equivalent to or even better than that of Serviflex (trade name of a Selby product in France), which is currently known as the best asbestos treatment agent. there were.
初w1a度124 f/I!
1時間後 14 #
48時間後 8 〃
実施例 2
吹付はアスベスト断片を磨砕し、前記実施例1と同様の
方法で発塵させ、2時間拡散し、アスベスト濃度が安定
したところを初期濃度とした。First w1a degree 124 f/I! After 1 hour 14 # After 48 hours 8 〃 Example 2 For spraying, asbestos fragments were ground up, dust was generated in the same manner as in Example 1, and the asbestos concentration was dispersed for 2 hours, and when the asbestos concentration stabilized, it was determined as the initial concentration. did.
実施例1と同様にしてアスベスト濃度を測定した。Asbestos concentration was measured in the same manner as in Example 1.
初期濃度 139 f/i!
1時間後 37
48時間後 12 〃
実施例 3
塊状アスベストの上部表面72.3cmの表面を別のコ
ンクリート上で荒く削り、細かい粉塵を発生するように
して試料とし、前記実施例と同様にして初FNfi度を
測定した。しかる後マンナン溶液を塊状片に噴霧し、上
記を同様の方法で発塵させ濃度を測定した。Initial concentration 139 f/i! After 1 hour 37 After 48 hours 12 〃 Example 3 A sample was prepared by roughly scraping the top surface of 72.3 cm of massive asbestos on another concrete surface to generate fine dust. The FNfi degree was measured. Thereafter, the mannan solution was sprayed onto the lumps, and the dust was generated in the same manner as above, and the concentration was measured.
初期濃度 453 1712
1時間後 73 〃
48時間後 56 〃
比較例
実施例3と同様な塊状アスベストを用いXンナン溶液に
代えて水を噴霧し、実施例3と同様にしてアスベスト濃
度を測定した。Initial concentration 453 1712 After 1 hour 73 After 48 hours 56 Comparative example Using the same lump asbestos as in Example 3, water was sprayed instead of the X-nannan solution, and the asbestos concentration was measured in the same manner as in Example 3.
初期濃度 92 r/1
噴霧直後 22 〃
1時間後 15 〃
20時間後 61 〃
前記比較例の結果から水噴霧によるアスベストの捕集効
果が時間の経過とともに低下しており、これは乾燥によ
るアスベストの再飛散によるものであり、単なる水の噴
霧はアスベスト粉塵対策としては十分でない。Initial concentration 92 r/1 Immediately after spraying 22 〃 After 1 hour 15 〃 After 20 hours 61 〃 From the results of the above comparative example, the asbestos collection effect by water spray decreases over time, and this is due to the asbestos being removed by drying. This is due to re-dispersion, and simple water spraying is not sufficient as a countermeasure against asbestos dust.
塊状アスベストのマンナン溶液吸収試験アスベスト粉塵
飛散防止のための、こんにゃくマンナン溶液の必要量を
決定するため塊状アスベスト単位体積当たりの前記各実
施例で用いた0、5%こんにゃくマンナン溶液の吸収量
を求めた。Mannan solution absorption test for lump asbestos In order to determine the required amount of konjac mannan solution to prevent asbestos dust scattering, the absorbed amount of the 0.5% konjac mannan solution used in each of the above examples per unit volume of lump asbestos was determined. Ta.
マンナン溶液 5 cc/ 4 cd−1,22cc
/ cd水 3 cc / 5 aj−
+0.61cc / ajアスベストが水に濡れにくい
という性質もまた、この結果に現れている。マンナン溶
液の吸収量がアスベスト片の体積を上回るのは表面を均
一にマンナン溶液が濡らし、容易に滴下しないためで、
実際のアスベスト対策に使用した場合の有効な特性の一
つである。Mannan solution 5 cc/4 cd-1,22cc
/ cd water 3 cc / 5 aj-
+0.61cc/aj The property that asbestos is difficult to get wet with water is also reflected in this result. The reason why the amount of mannan solution absorbed exceeds the volume of the asbestos piece is because the mannan solution wets the surface uniformly and does not drip easily.
This is one of the effective characteristics when used in actual asbestos countermeasures.
このような−例の実験結果に基いた本発明のこんにゃく
精粉もしくはその誘導体の水溶液濃度は0.2〜2χ、
好ましくは0.4〜0.7χであった。Based on the experimental results of these examples, the concentration of the aqueous solution of the konjac flour of the present invention or its derivatives is 0.2 to 2χ,
Preferably it was 0.4 to 0.7χ.
(発明の効果)
本発明によれば建築物の解体、改修時におけるアスベス
ト粉塵の飛散を効果的に防止することができる。(Effects of the Invention) According to the present invention, it is possible to effectively prevent asbestos dust from scattering during the demolition and renovation of buildings.
また散水によっても不充分なアスベスト層内部への発塵
防止もその浸透性によって可能となし、剥離、除去作業
において作業の進行とともに薬液を追加噴霧する必要が
ない等の作業能率の向上、作業コストの低廉を計ること
ができる。In addition, its permeability prevents dust from forming inside the asbestos layer, which is insufficient even with water spraying, and improves work efficiency and costs, such as eliminating the need to spray additional chemicals as the work progresses during stripping and removal work. can be measured at low cost.
Claims (4)
発生する粉塵の飛散を防止せしめる方法に於いて、こん
にゃく精粉もしくはその誘導体水溶液を建造物に噴霧す
ることを特徴とするアスベスト粉塵の飛散防止方法。(1) A method for preventing the scattering of asbestos dust, which is characterized by spraying konjac fine powder or an aqueous solution of its derivatives onto the structure, in a method for preventing the scattering of dust generated during the demolition or renovation of buildings containing asbestos. Method.
及び/又は界面活性剤等の補助剤を加える前記請求項1
記載の方法。(2) For the aqueous solution, a protective colloid agent, a preservative,
Claim 1 wherein an auxiliary agent such as a surfactant and/or a surfactant is added.
Method described.
なるアスベスト粉塵の飛散防止用処理剤。(3) A treatment agent for preventing scattering of asbestos dust consisting of an aqueous solution of fine konjac powder or its derivatives.
して、保護コロイド剤、防腐剤及び/又は界面活性剤等
の補助剤を含有させた前記請求項3記載の処理剤。(4) The treatment agent according to claim 3, wherein an auxiliary agent such as a protective colloid, a preservative, and/or a surfactant is added to the aqueous solution of fine konjac powder or a derivative thereof.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1033646A JPH02214584A (en) | 1989-02-15 | 1989-02-15 | Method for preventing scattering of asbestos dust and dust treating agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1033646A JPH02214584A (en) | 1989-02-15 | 1989-02-15 | Method for preventing scattering of asbestos dust and dust treating agent |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02214584A true JPH02214584A (en) | 1990-08-27 |
Family
ID=12392209
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1033646A Pending JPH02214584A (en) | 1989-02-15 | 1989-02-15 | Method for preventing scattering of asbestos dust and dust treating agent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02214584A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007130554A (en) * | 2005-11-09 | 2007-05-31 | Mia Kikaku Kk | Treating agent for acicular crystal and method and apparatus for treating acicular crystal |
JP2008155143A (en) * | 2006-12-25 | 2008-07-10 | M-Tec:Kk | Treatment method of hardened cement body and processed substance |
JP2010185182A (en) * | 2009-02-10 | 2010-08-26 | Shimizu Corp | Method for removing spraying material containing asbestos |
US8578582B2 (en) | 2009-09-02 | 2013-11-12 | Nippon Steel Engineering Co., Ltd. | Method of demolishing furnace of multilayered-refractory structure |
-
1989
- 1989-02-15 JP JP1033646A patent/JPH02214584A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007130554A (en) * | 2005-11-09 | 2007-05-31 | Mia Kikaku Kk | Treating agent for acicular crystal and method and apparatus for treating acicular crystal |
JP2008155143A (en) * | 2006-12-25 | 2008-07-10 | M-Tec:Kk | Treatment method of hardened cement body and processed substance |
JP2010185182A (en) * | 2009-02-10 | 2010-08-26 | Shimizu Corp | Method for removing spraying material containing asbestos |
US8578582B2 (en) | 2009-09-02 | 2013-11-12 | Nippon Steel Engineering Co., Ltd. | Method of demolishing furnace of multilayered-refractory structure |
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