JPH0512307B2 - - Google Patents
Info
- Publication number
- JPH0512307B2 JPH0512307B2 JP30061888A JP30061888A JPH0512307B2 JP H0512307 B2 JPH0512307 B2 JP H0512307B2 JP 30061888 A JP30061888 A JP 30061888A JP 30061888 A JP30061888 A JP 30061888A JP H0512307 B2 JPH0512307 B2 JP H0512307B2
- Authority
- JP
- Japan
- Prior art keywords
- asbestos
- acid
- treatment agent
- acids
- modification treatment
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000010425 asbestos Substances 0.000 claims description 64
- 229910052895 riebeckite Inorganic materials 0.000 claims description 64
- 239000002253 acid Substances 0.000 claims description 29
- 239000003795 chemical substances by application Substances 0.000 claims description 26
- 150000007513 acids Chemical class 0.000 claims description 20
- 230000004048 modification Effects 0.000 claims description 19
- 238000012986 modification Methods 0.000 claims description 19
- 150000001875 compounds Chemical class 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 12
- 229920000592 inorganic polymer Polymers 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 11
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 150000002367 halogens Chemical class 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 239000011593 sulfur Substances 0.000 claims description 6
- 229910004298 SiO 2 Inorganic materials 0.000 description 10
- 239000007864 aqueous solution Substances 0.000 description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- 229910052620 chrysotile Inorganic materials 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- CWBIFDGMOSWLRQ-UHFFFAOYSA-N trimagnesium;hydroxy(trioxido)silane;hydrate Chemical compound O.[Mg+2].[Mg+2].[Mg+2].O[Si]([O-])([O-])[O-].O[Si]([O-])([O-])[O-] CWBIFDGMOSWLRQ-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000000835 fiber Substances 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-M Trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-M 0.000 description 2
- 238000002441 X-ray diffraction Methods 0.000 description 2
- XYCWOLUUHSNDRX-UHFFFAOYSA-L [dioxido-[oxo(trioxidosilyloxy)silyl]oxysilyl]oxy-[[dioxido-[oxo(trioxidosilyloxy)silyl]oxysilyl]oxy-oxosilyl]oxy-dioxidosilane iron(2+) dihydroxide Chemical compound [OH-].[OH-].[Fe++].[Fe++].[Fe++].[Fe++].[Fe++].[Fe++].[Fe++].[O-][Si]([O-])([O-])O[Si](=O)O[Si]([O-])([O-])O[Si](=O)O[Si]([O-])([O-])O[Si]([O-])([O-])O[Si](=O)O[Si]([O-])([O-])[O-] XYCWOLUUHSNDRX-UHFFFAOYSA-L 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- -1 alkyl silicate Chemical compound 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 2
- 229910001634 calcium fluoride Inorganic materials 0.000 description 2
- 239000004568 cement Substances 0.000 description 2
- 229910052681 coesite Inorganic materials 0.000 description 2
- 229910052906 cristobalite Inorganic materials 0.000 description 2
- 239000002440 industrial waste Substances 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229910052682 stishovite Inorganic materials 0.000 description 2
- 229910052905 tridymite Inorganic materials 0.000 description 2
- ULEFFCDROVNTRO-UHFFFAOYSA-N trimagnesium;disodium;dihydroxy(oxo)silane;iron(3+) Chemical compound [Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Fe+3].[Fe+3].O[Si](O)=O.O[Si](O)=O.O[Si](O)=O.O[Si](O)=O.O[Si](O)=O.O[Si](O)=O.O[Si](O)=O.O[Si](O)=O ULEFFCDROVNTRO-UHFFFAOYSA-N 0.000 description 2
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 1
- 229910018557 Si O Inorganic materials 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- 241001122767 Theaceae Species 0.000 description 1
- 229910003077 Ti−O Inorganic materials 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 229940071870 hydroiodic acid Drugs 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229910000358 iron sulfate Inorganic materials 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- MVFCKEFYUDZOCX-UHFFFAOYSA-N iron(2+);dinitrate Chemical compound [Fe+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MVFCKEFYUDZOCX-UHFFFAOYSA-N 0.000 description 1
- SHXXPRJOPFJRHA-UHFFFAOYSA-K iron(iii) fluoride Chemical compound F[Fe](F)F SHXXPRJOPFJRHA-UHFFFAOYSA-K 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 229910052751 metal Chemical class 0.000 description 1
- 239000002184 metal Chemical class 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- LLYCMZGLHLKPPU-UHFFFAOYSA-N perbromic acid Chemical compound OBr(=O)(=O)=O LLYCMZGLHLKPPU-UHFFFAOYSA-N 0.000 description 1
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical compound OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 description 1
- 150000004968 peroxymonosulfuric acids Chemical class 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Inorganic materials [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 1
- 239000010454 slate Substances 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Inorganic materials O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 1
- HIFJUMGIHIZEPX-UHFFFAOYSA-N sulfuric acid;sulfur trioxide Chemical compound O=S(=O)=O.OS(O)(=O)=O HIFJUMGIHIZEPX-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Landscapes
- Processing Of Solid Wastes (AREA)
Description
【発明の詳細な説明】
[産業上の利用分野]
この発明は、石綿の改質処理剤及び処理方法に
係り、より詳しくは、主として産業廃棄物として
処置された建築構造物の壁、天井等から除去され
た吹付け石綿、スレート板、ブレーキシユー等の
不要となつた石綿含有物質を改質して無害化する
ための処理剤及び処理方法に関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to an asbestos modification treatment agent and treatment method, and more specifically, it relates to an asbestos modification treatment agent and a treatment method, and more specifically, it is mainly used for asbestos treatment for walls, ceilings, etc. of building structures that are treated as industrial waste. The present invention relates to a treatment agent and a treatment method for modifying and rendering harmless asbestos-containing materials that are no longer needed, such as sprayed asbestos, slate boards, brake shoes, etc.
[従来の技術]
石綿には、一般にアスベストとして従来から広
く使用されている白石綿(クリソタイル、
MgO・SiO2を主成分とするもの)のほかに、少
量ではあるが、茶石綿(アモサイト、Fe2O3・
SiO2を主成分とするもの)、青石綿(クロシドラ
イト、Fe2O3・SiO2を主成分とするもの)等も使
用されており、耐火性、耐久性、断熱性、耐摩耗
性等の長所を有する天然繊維として優れた特性を
有している。このため、このような石綿は、成形
板として、あるいは、耐火被覆、吸音材料、断熱
材料等の吹付け材料等として建築関係の分野で幅
広く使用されてきた。[Conventional technology] Asbestos includes white asbestos (chrysotile,
In addition to asbestos (mainly composed of MgO and SiO 2 ), there is also a small amount of tea asbestos (amosaite, Fe 2 O 3 ,
SiO 2 as the main component), blue asbestos (crocidolite, Fe 2 O 3 / SiO 2 as the main component), etc. are also used, and they have properties such as fire resistance, durability, heat insulation, and abrasion resistance. It has excellent properties as a natural fiber with advantages. For this reason, such asbestos has been widely used in construction-related fields as molded plates or as sprayed materials such as fireproof coatings, sound-absorbing materials, and heat-insulating materials.
しかしながら、このような石綿は針状繊維の粉
塵の発生原因となり、この針状繊維が粉塵となつ
て人体に取込まれると健康に悪影響を及ぼすこと
がわかり、この石綿公害が大きな社会問題となつ
てきた。 However, such asbestos causes the generation of acicular fiber dust, and it has been found that when this acicular fiber becomes dust and is taken into the human body, it has an adverse effect on health, and this asbestos pollution has become a major social problem. It's here.
このため、従来すでに用いられた石綿含有物質
について、これを除去して廃棄しようとする考え
が生じ、これまでに除去されて廃棄物となつた石
綿含有物質を袋詰めやコンクリート詰めにして土
中に埋める等の方法が試みられてきた。 For this reason, the idea of removing and disposing of the asbestos-containing materials that have already been used has arisen, and the asbestos-containing materials that have been removed and become waste are packed in bags or concrete and buried in the soil. Several methods have been tried, such as burying the
しかしながら、このような方法での石綿含有物
質の処理は、何らかの機会、例えば地震等によつ
て土中から地表に露出し、再び粉塵となつて公害
発生の原因となる可能性もあり、地方自治体によ
つては、このような方法での石綿含有物質の廃棄
処理を禁止するところもでてきた。このため、石
綿含有物質をいかにして無害なものに処理できる
かが大きな課題となつていた。 However, when asbestos-containing materials are disposed of in this way, there is a possibility that they may be exposed from the soil to the surface due to some chance, such as an earthquake, and turn into dust again, causing pollution. In some cases, the disposal of asbestos-containing materials using this method has been banned. For this reason, how to treat asbestos-containing materials into harmless substances has become a major issue.
ところで、石綿は、化学的に極めて安定な物質
であり、弗化水素酸を除いては通常一般の酸に溶
解せず、化学的に改質することが極めて困難であ
ると考えられていたことから、これまでにこの石
綿を化学的に改質しようとする試みは全くなされ
ておらず、石綿の処理については根本的な解決に
は至つていないのが実情であつた。 By the way, asbestos is a chemically extremely stable substance that does not dissolve in ordinary acids except hydrofluoric acid, and was thought to be extremely difficult to modify chemically. Therefore, no attempt has been made to chemically modify this asbestos, and the reality is that no fundamental solution has been reached regarding the treatment of asbestos.
[発明が解決しようとする課題]
そこで、本発明者らは、石綿が塩基性物質であ
ることに着目し、石綿に含まれている塩基性成分
もMgOやFe2O3と反応し、しかも、この石綿の
表面を覆つていると考えられるSiO2あるいはこ
のSiO2とMgO若しくはFe2O3化合物を化学的あ
るいは物理的に破壊できないかという観点から、
種々の物質について鋭意検討した結果、本発明に
到達したものである。[Problems to be Solved by the Invention] Therefore, the present inventors focused on the fact that asbestos is a basic substance, and found that the basic component contained in asbestos also reacts with MgO and Fe 2 O 3 . From the viewpoint of whether it is possible to chemically or physically destroy the SiO 2 or the SiO 2 and MgO or Fe 2 O 3 compounds that are thought to cover the surface of asbestos,
The present invention was arrived at as a result of intensive studies on various substances.
従つて、本発明の目的は、石綿自体を化学的に
改質し無害化することができる石綿の改質処理剤
を提供することにある。 Therefore, an object of the present invention is to provide an asbestos modification treatment agent that can chemically modify asbestos itself and render it harmless.
また、本発明の他の目的は、このような改質処
理剤を使用して石綿を化学的に改質し無害化する
石綿の改質処理方法を提供することにある。 Another object of the present invention is to provide a method for modifying asbestos, which uses such a modifying agent to chemically modify asbestos and render it harmless.
[課題を解決するための手段]
すなわち、本発明は、硫黄、窒素又はハロゲン
のいずれか1種又は2種以上の元素を有する酸の
1種又は2種以上の混合物、水性無機高分子化合
物の1種又は2種以上の混合物とを含有する石綿
の改質処理剤であり、また、このような改質処理
剤を繊維状の石綿に接触させて反応させることに
より、この石綿を塊状化させつつ固結化させる石
綿の改質処理方法である。[Means for Solving the Problems] In other words, the present invention provides a solution to a mixture of one or more acids having one or more elements of sulfur, nitrogen, or halogen, and an aqueous inorganic polymer compound. It is an asbestos modification treatment agent containing one type or a mixture of two or more types, and by bringing such a modification treatment agent into contact with fibrous asbestos and causing a reaction, this asbestos is made into agglomerates. This is a method for modifying asbestos by solidifying it.
本発明で使用する硫黄、窒素又はハロゲンのい
ずれか1種又は2種以上の元素を有する酸とは、
これらの元素のいずれかを有し、水溶液の状態で
酸としての性質を示すものをいい、硫黄を含む酸
としては例えば硫黄、無水硫酸、発煙硫酸、過硫
酸、亜硫酸等を挙げることができ、また、窒素を
含む酸としては例えば硝酸、発煙硝酸、亜硝酸等
を挙げることができ、さらに、ハロゲンを含む酸
としては例えば弗化水素酸、塩酸、臭化水素酸、
沃化水素酸、過弗素酸、過塩素酸、過臭素酸、過
沃素酸等を挙げることができる。これらの酸類
は、その1種のみで使用できるほか、2種以上を
併用した混合物としても使用でき、さらには、こ
れらの酸類のアンモニウム塩や金属塩を併用使用
することもできる。 The acid containing one or more elements of sulfur, nitrogen, or halogen used in the present invention is:
It refers to something that has any of these elements and exhibits properties as an acid in an aqueous solution state. Examples of acids containing sulfur include sulfur, sulfuric anhydride, fuming sulfuric acid, persulfuric acid, and sulfurous acid. Further, examples of acids containing nitrogen include nitric acid, fuming nitric acid, nitrous acid, etc. Furthermore, examples of acids containing halogen include hydrofluoric acid, hydrochloric acid, hydrobromic acid,
Hydroiodic acid, perfluoric acid, perchloric acid, perbromic acid, periodic acid, etc. can be mentioned. These acids can be used alone or as a mixture of two or more, and ammonium salts and metal salts of these acids can also be used in combination.
なお、本発明で使用する酸は、石綿がMgO・
SiO2を主成分とするクリソタイル(白石綿)で
ある場合は、その塩基性が比較的強いでの、上記
いずれの酸類であつても好適に使用できるが、こ
の石綿が、一般にはあまり使用されず、また、使
用されたとしても極少量用いられるにすぎないも
のではあるが、上記クリソタイル以外の石綿、例
えばアモサイト(茶石綿)やクロシドライト(青
石綿)である場合には、これらがSiO2・Fe2O3を
主成分とし、その塩基性が弱く、通常の酸との反
応が遅く、なかなか改質が進まない場合があるの
で、このような場合には、弗素を含む酸、例えば
弗化水素酸、過弗素酸あるいは弗素を含む酸の塩
とその他の酸類との混合物を使用するのがよい。 Note that the acid used in the present invention is suitable for asbestos containing MgO and
In the case of chrysotile (white asbestos), which has SiO 2 as its main component, any of the acids mentioned above can be suitably used as its basicity is relatively strong, but this asbestos is not commonly used. Furthermore, although it is used only in extremely small quantities, if asbestos other than the above-mentioned chrysotile is used, such as amosite (brown asbestos) or crocidolite (blue asbestos), these may be SiO 2 . Fe 2 O 3 is the main component, and its basicity is weak, so it reacts slowly with ordinary acids, and the modification may not proceed easily. Hydrogen acid, perfluoric acid or a mixture of a salt of a fluorine-containing acid and other acids is preferably used.
また、本発明において、上記酸類と共に使用す
る水性無機高分子化合物は、水溶性又は水分散性
を有し、かつ、分子内にSi−O,Ti−O,Al−
O等の結合を少なくとも1種以上有する高分子化
合物であり、水に溶解あるいは分散させた際に高
分子として水中に溶解あるいはコロイド状に分散
しており、乾燥すれば固結化してそれ自体が皮膜
を形成する能力を有するものである。この水性無
機高分子化合物の水溶性あるいは水分散液として
は、例えば水ガラス、アルキルシリケート部分加
水分解物水溶液、コロイダルシリカ、アルキルチ
タネート部分加水分解物水溶液、チタニアゾル、
アルミナゾル等を挙げることができ、その1種の
みを単独で使用することもできるし、また、2種
以上の混合物としても使用することもできる。 In addition, in the present invention, the aqueous inorganic polymer compound used together with the above acids has water solubility or water dispersibility, and has Si-O, Ti-O, Al-
It is a polymer compound that has at least one type of bond such as O, etc. When dissolved or dispersed in water, it is dissolved or dispersed in water as a polymer or dispersed in the form of a colloid, and when dried, it solidifies and forms itself. It has the ability to form a film. Examples of the water-soluble or water-dispersed liquid of this aqueous inorganic polymer compound include water glass, aqueous solution of alkyl silicate partial hydrolyzate, colloidal silica, aqueous solution of alkyl titanate partial hydrolyzate, titania sol,
Examples include alumina sol, which can be used alone or as a mixture of two or more.
本発明の改質処理剤を製造するに当つては、先
ず、上記酸類の水溶液に上記水性無機高分子化合
物の水溶液あるいは水分酸性液を攪拌しながら添
加し、充分に混合する。この際に、水性無機高分
子化合物がゲル化して沈澱することがあるので、
攪拌は十分に行なう必要がある。 In producing the modification treatment agent of the present invention, first, the aqueous solution of the aqueous inorganic polymer compound or water acidic liquid is added to the aqueous solution of the acid with stirring, and mixed thoroughly. At this time, the aqueous inorganic polymer compound may gel and precipitate.
It is necessary to stir sufficiently.
本発明の改質処理剤において、酸類の濃度はそ
の反応性を考慮すると、PHが3.5以下、好ましく
は3.0〜0.5の範囲となるようにするのが適当であ
る。PHが0.5より低いと、水性無機高分子化合物
の水溶液あるいは水分散液が安定に存在すること
が難しくなり、ゲル化が起つて沈澱物が生成し易
くなる。また、水性無機高分子化合物の濃度につ
いては、改質処理剤の水溶液又は水分散液中固形
分として0.5〜20重量%、好ましくは1〜10重量
%程度がよい。この使用量が0.5重量%より少な
いと石綿の改質処理能力が不足し、また、20重量
%より多いと水溶液又は水分散液中でゲル化し沈
澱する場合があつて好ましくない。 In the modifying treatment agent of the present invention, the concentration of acids is appropriately set such that the pH thereof is 3.5 or less, preferably in the range of 3.0 to 0.5, taking into account its reactivity. When the pH is lower than 0.5, it becomes difficult for an aqueous solution or aqueous dispersion of an aqueous inorganic polymer compound to exist stably, and gelation occurs and precipitates are likely to be formed. The concentration of the aqueous inorganic polymer compound is preferably about 0.5 to 20% by weight, preferably about 1 to 10% by weight as a solid content in the aqueous solution or dispersion of the modifying agent. If the amount used is less than 0.5% by weight, the ability to modify asbestos will be insufficient, and if it is more than 20% by weight, it may gel and precipitate in an aqueous solution or dispersion, which is not preferable.
本発明において、改質処理剤を使用して石綿を
処理するには、この改質処理剤をそのまま石綿に
噴霧又は塗布するか、あるいは、この石綿を攪拌
及び/又は粉砕しながらこの改質処理剤を作用さ
せるのがよく、この際に改質処理剤の石綿への反
応性を高めるために必要により改質処理剤及び/
又は合いを適当な温度に加温することもできる。 In the present invention, in order to treat asbestos using a modification treatment agent, the modification treatment agent may be sprayed or applied directly onto the asbestos, or the modification treatment may be carried out while stirring and/or pulverizing the asbestos. At this time, in order to increase the reactivity of the modifying agent to asbestos, if necessary, the modifying agent and/or
Alternatively, the mixture can be heated to an appropriate temperature.
なお、本発明の改質処理剤と石綿との反応が終
了して余剰の酸が残つた場合には、石灰等を用い
て中和し、また、窒素、ハロゲンを含む酸類を用
いた場合は石綿との反応生成物が水に可溶性であ
る場合が多いので、改質処理剤中に適量の水溶性
あるいは水分散性の有機高分子化合物、例えばポ
リアクリルアミド、ポリビニルブチラール部分加
水分解物、ポリアクリルエマルジヨン等を添加し
ておき、乾燥後には水不溶性の皮膜を形成せしめ
て封じ込めることも可能である。 In addition, if the reaction between the modification treatment agent of the present invention and asbestos is completed and surplus acid remains, neutralize it using lime etc. Also, if acids containing nitrogen or halogen are used, Since reaction products with asbestos are often soluble in water, an appropriate amount of water-soluble or water-dispersible organic polymer compounds, such as polyacrylamide, polyvinyl butyral partial hydrolyzate, polyacrylic, is added to the modification treatment agent. It is also possible to add an emulsion or the like and form a water-insoluble film after drying for sealing.
さらに、この改質処理剤は、場合により石綿を
廃棄しないで、その表面に吹付け層等の被覆層を
形成せしめ、その状態のまま補修し、あるいは、
封じ込み処理する場合に適用することができる。
この場合でも、改質処理剤を噴霧あるいは塗布し
て石綿を塊状化させつつ改質させることができ
る。 Furthermore, this modification treatment agent can, in some cases, form a coating layer such as a spray layer on the surface of asbestos without disposing of it, and repair it in that state, or
It can be applied when carrying out containment processing.
Even in this case, the asbestos can be modified while being agglomerated by spraying or applying the modifying agent.
[作用]
本発明の改質処理剤で石綿を処理すると、針状
繊維状の石綿が溶解しつつ固化する際に塊状物質
となる。そして、この理由については、以下のよ
うに考察することができる。[Function] When asbestos is treated with the modifying treatment agent of the present invention, the acicular fibrous asbestos dissolves and solidifies into a lumpy substance. The reason for this can be considered as follows.
すなわち、例えば石綿がクリソタイルである場
合、その石綿がMgO・SiO2を主成分とし塩基性
であるにもかかわらず通常の酸に溶解しない理由
については、その表面が通常の酸には溶解し難い
SiO2を主成分とする皮膜で覆われているからで
あると考えられている。 In other words, for example, if asbestos is chrysotile, the reason why it does not dissolve in ordinary acids even though it is basic and contains MgO/SiO 2 as its main component is that its surface is difficult to dissolve in ordinary acids.
It is thought that this is because it is covered with a film whose main component is SiO 2 .
しかるに、上記酸類と水性無機高分子化合物を
含有する水溶液あるいは水分散液からなる本発明
の改質処理剤でこの石綿を処理すると、無機高分
子化合物が石綿表面で固結化して皮膜を形成する
際に収縮応力が発生する。そして、この収縮応力
は、石綿表面に存在する通常の酸には溶解し難い
上記皮膜に微細な亀裂を生起せしめ、そこに活性
点が発生し、そこから酸類が侵入し、石綿内部に
存在する塩基性のMgO・SiO2と反応してMgの酸
塩を形成するものと考えられる。 However, when this asbestos is treated with the modifying agent of the present invention, which is an aqueous solution or aqueous dispersion containing the above-mentioned acids and an aqueous inorganic polymer compound, the inorganic polymer compound solidifies on the asbestos surface to form a film. Shrinkage stress occurs during this process. This shrinkage stress causes minute cracks in the film that is difficult to dissolve in normal acids that exists on the surface of asbestos, and active points are generated there, through which acids can enter and destroy the asbestos that exists inside the asbestos. It is thought that it reacts with basic MgO/SiO 2 to form an acid salt of Mg.
[実施例]
以下、実施例に基づいて、本発明を具体的に説
明する。[Example] Hereinafter, the present invention will be specifically described based on Examples.
実施例 1
白石綿(クリソタイル)40重量%とセメント60
重量%とを含む吹付け石綿の除去物を供試体とし
た。Example 1 White asbestos (chrysotile) 40% by weight and cement 60%
The test piece was a product from which sprayed asbestos was removed, which contained % by weight.
改質処理剤として下記組成(固形分換算重量
%)のものを調製した。 A modification treatment agent having the following composition (weight % in terms of solid content) was prepared.
硫酸 ……15wt%
過硫酸アンモン ……5wt%
シリカゾル(SiO2として) ……10wt%
この改質処理剤を上記の供試体石綿に対して重
量比で80%添加し、80℃に加温して1時間攪拌し
た後、乾燥固化させた。 Sulfuric acid: 15 wt% Ammonium persulfate: 5 wt% Silica sol (as SiO2): 10 wt% This modification treatment agent was added to the above asbestos specimen at a weight ratio of 80%, and heated to 80°C. After stirring for 1 hour, it was dried and solidified.
固化後の供試体の成分をX線回析法で分析した
ところ、クリソタイルは検出不能となつており、
代りに硫酸マグネシウムとシリカ、及び、微量の
硫酸カルシウムと硫酸鉄が検出され、針状繊維状
であつた供試体は塊状に固結化していた。 When the components of the specimen after solidification were analyzed using X-ray diffraction, chrysotile was undetectable.
Instead, magnesium sulfate and silica, as well as trace amounts of calcium sulfate and iron sulfate were detected, and the acicular fibrous specimen had solidified into a lump.
従つて、この改質処理により、針状繊維状の石
綿は塊状に改質され、また、その組成も上記の通
りに無害化されており、このような状態で固結化
していることが判明した。 Therefore, through this modification process, the acicular fibrous asbestos was modified into lumps, and its composition was also rendered harmless as described above, and it was found that it solidified in this state. did.
実施例 2
茶石綿(アモサイト)40重量%とセメント60重
量%とを含む吹付け石綿の除去物を供試体とし
た。Example 2 A specimen was prepared from sprayed asbestos containing 40% by weight of brown asbestos (amosite) and 60% by weight of cement.
改質処理剤として下記組成(固形分換算重量
%)のものを調製した。 A modification treatment agent having the following composition (weight % in terms of solid content) was prepared.
弗化水素酸 ……10wt%
硝酸 ……5wt%
エチルシリケート部分加水分
解物(SiO2として) ……5wt%
この改質処理剤を上記の供試体石綿に対して重
量比で70%添加し、70℃に加温して1時間攪拌し
た後、乾燥固化させた。 Hydrofluoric acid...10wt% Nitric acid...5wt% Ethylsilicate partial hydrolyzate (as SiO2 )...5wt% This modification treatment agent was added to the asbestos specimen above at a weight ratio of 70%. After heating to 70°C and stirring for 1 hour, the mixture was dried and solidified.
固化終了後、供試体に対し、余剰の酸を中和す
るための石灰を10重量%(固形分換算重量%)、
及び、5wt%−アクリルエマルジヨン水溶液を20
%それぞれ攪拌しながら添加し、乾燥固化させ
た。このようにして弗化物は弗化カルシウムとし
て、また、硝酸塩はアクリルエマルジヨンに封じ
込み、水難溶性の物質に改質した。 After solidification, 10% by weight of lime (solid content equivalent weight%) was added to the specimen to neutralize excess acid.
And 20% of 5wt% acrylic emulsion aqueous solution
% was added with stirring and dried and solidified. In this way, the fluoride was encapsulated in the form of calcium fluoride, and the nitrate was encapsulated in the acrylic emulsion, thereby modifying it into a poorly water-soluble substance.
得られた処理物は塊状に固化しており、X線回
析法による分析の結果、アモサイトは検出不能で
あり、代りに硫酸カルシウム、酸化カルシウム、
弗化カルシウム、硝酸鉄、弗化鉄、シリカ等の特
性ピークが認められた。 The obtained treated product solidified into lumps, and as a result of analysis by X-ray diffraction method, amosite was undetectable, and calcium sulfate, calcium oxide,
Characteristic peaks of calcium fluoride, iron nitrate, iron fluoride, silica, etc. were observed.
[発明の効果]
本発明によれば、石綿含有物質を産業廃棄物と
して廃棄処理する際に、その針状繊維の粉塵を飛
散させることなく塊状化、固結化すると共に、こ
の針状繊維を改質無害化することができ、実用上
の効果は極めて顕著である。[Effects of the Invention] According to the present invention, when asbestos-containing materials are disposed of as industrial waste, the acicular fibers are agglomerated and solidified without scattering, and the acicular fibers are It can be modified to make it harmless, and the practical effect is extremely significant.
Claims (1)
2種以上の元素を有する酸の1種又は2種以上の
混合物と、水性無機高分子化合物の1種又は2種
以上の混合物とを含有することを特徴とする石綿
の改質処理剤。 2 硫黄、窒素又はハロゲンのいずれか1種又は
2種以上の元素を有する酸の1種又は2種以上の
混合物と水性無機高分子化合物の1種又は2種以
上の混合物とを含有する処理剤を、繊維状の石綿
に接触させて反応させることにより、この石綿を
塊状化させつつ固結化させることを特徴とする石
綿の改質処理方法。[Scope of Claims] 1. One or more mixtures of acids containing one or more elements of sulfur, nitrogen, or halogen, and one or more aqueous inorganic polymer compounds. An asbestos modification treatment agent characterized by containing a mixture thereof. 2. A treatment agent containing one or a mixture of two or more acids containing one or more elements of sulfur, nitrogen, or halogen, and one or a mixture of two or more aqueous inorganic polymer compounds. 1. A method for modifying asbestos, which comprises bringing the asbestos into contact with fibrous asbestos and reacting with the asbestos, thereby clumping and solidifying the asbestos.
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP30061888A JPH02149483A (en) | 1988-11-30 | 1988-11-30 | Asbestos modification treatment agent and modification treatment method |
| EP89904234A EP0372084B1 (en) | 1988-04-30 | 1989-04-11 | Asbestos-treating agent and process for treating asbestos |
| DE68917433T DE68917433T2 (en) | 1988-04-30 | 1989-04-11 | METHOD FOR TREATING ASBEST AND ASBEST TREATMENT. |
| AU33695/89A AU3369589A (en) | 1988-04-30 | 1989-04-11 | Asbestos-treating agent and process for treating asbestos |
| PCT/JP1989/000388 WO1989010338A1 (en) | 1988-04-30 | 1989-04-11 | Asbestos-treating agent and process for treating asbestos |
| CN89103001A CN1038080A (en) | 1988-04-30 | 1989-04-29 | Asbestos treatment agent and treatment process |
| KR1019890702465A KR900700406A (en) | 1988-04-30 | 1989-12-27 | Asbestos treatment agent and treatment method |
| NO89895282A NO895282L (en) | 1988-04-30 | 1989-12-27 | PROCEDURE FOR DIMMING ASBEST DUST. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP30061888A JPH02149483A (en) | 1988-11-30 | 1988-11-30 | Asbestos modification treatment agent and modification treatment method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH02149483A JPH02149483A (en) | 1990-06-08 |
| JPH0512307B2 true JPH0512307B2 (en) | 1993-02-17 |
Family
ID=17887026
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP30061888A Granted JPH02149483A (en) | 1988-04-30 | 1988-11-30 | Asbestos modification treatment agent and modification treatment method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH02149483A (en) |
-
1988
- 1988-11-30 JP JP30061888A patent/JPH02149483A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPH02149483A (en) | 1990-06-08 |
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