JPS6116681B2 - - Google Patents
Info
- Publication number
- JPS6116681B2 JPS6116681B2 JP14525982A JP14525982A JPS6116681B2 JP S6116681 B2 JPS6116681 B2 JP S6116681B2 JP 14525982 A JP14525982 A JP 14525982A JP 14525982 A JP14525982 A JP 14525982A JP S6116681 B2 JPS6116681 B2 JP S6116681B2
- Authority
- JP
- Japan
- Prior art keywords
- coating
- deposits
- pretreatment agent
- open
- weight
- 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
Links
- 238000000576 coating method Methods 0.000 claims description 30
- 239000011248 coating agent Substances 0.000 claims description 28
- 239000003795 chemical substances by application Substances 0.000 claims description 20
- 239000003973 paint Substances 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 8
- 150000001298 alcohols Chemical class 0.000 claims description 6
- 239000004480 active ingredient Substances 0.000 claims description 5
- 238000005507 spraying Methods 0.000 claims description 5
- 150000005846 sugar alcohols Polymers 0.000 claims description 5
- 238000001035 drying Methods 0.000 claims description 4
- 239000000843 powder Substances 0.000 description 9
- 239000003245 coal Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000013049 sediment Substances 0.000 description 4
- 239000000571 coke Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 238000004078 waterproofing Methods 0.000 description 3
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000002817 coal dust Substances 0.000 description 2
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- XLLIQLLCWZCATF-UHFFFAOYSA-N ethylene glycol monomethyl ether acetate Natural products COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- -1 summer heat Substances 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 description 1
- LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 1
- FPZWZCWUIYYYBU-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl acetate Chemical compound CCOCCOCCOC(C)=O FPZWZCWUIYYYBU-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- HRWADRITRNUCIY-UHFFFAOYSA-N 2-(2-propan-2-yloxyethoxy)ethanol Chemical compound CC(C)OCCOCCO HRWADRITRNUCIY-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- HXDLWJWIAHWIKI-UHFFFAOYSA-N 2-hydroxyethyl acetate Chemical compound CC(=O)OCCO HXDLWJWIAHWIKI-UHFFFAOYSA-N 0.000 description 1
- HCGFUIQPSOCUHI-UHFFFAOYSA-N 2-propan-2-yloxyethanol Chemical compound CC(C)OCCO HCGFUIQPSOCUHI-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000001151 other effect Effects 0.000 description 1
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65G—TRANSPORT OR STORAGE DEVICES, e.g. CONVEYORS FOR LOADING OR TIPPING, SHOP CONVEYOR SYSTEMS OR PNEUMATIC TUBE CONVEYORS
- B65G3/00—Storing bulk material or loose, i.e. disorderly, articles
- B65G3/02—Storing bulk material or loose, i.e. disorderly, articles in the open air
Description
【発明の詳細な説明】
この発明は石炭、コークス、鉄鉱石、川砂のよ
うな鉱物、木粉などを長期間に亘り野積堆積させ
る際に、これら堆積物の表面上に塗工して堆積物
の防水、防塵、空気による酸化防止などを図るた
めの被覆用前処理剤とこれを用いた被覆方法に関
するものである。Detailed Description of the Invention This invention is a method of coating coal, coke, iron ore, minerals such as river sand, wood powder, etc., when depositing them in open piles over a long period of time. The present invention relates to a coating pretreatment agent for waterproofing, dustproofing, preventing oxidation caused by air, etc., and a coating method using the same.
一般に製鉄所、ガス製造所、製紙工場などでは
石炭、コークス、木粉などを野積堆積して保管す
る場合が多い。ところが、これらの堆積物はその
保管中に風によつて粉塵を巻きおこして周辺地域
への粉塵公害をおこしたり堆積物のロスを招きや
すく、また降雨時には河川や海に流れ出して汚水
の原因になつたり、石炭、コークス、鉄鉱石など
の堆積物中の含水量が過剰となるとこれを燃焼さ
せる場合に水の蒸発熱損を生じるなどの不都合が
ある。 In general, coal, coke, wood powder, etc. are often stored in open piles at steel mills, gas plants, paper mills, etc. However, during storage, these sediments tend to stir up dust in the wind, causing dust pollution in surrounding areas and causing sediment loss, and during rainfall, they flow into rivers and the sea, causing sewage. Excessive moisture content in sediments such as summer heat, coal, coke, iron ore, etc., causes disadvantages such as evaporative heat loss of water when the deposits are combusted.
これらの問題を解決するすぐれた方法として、
野積堆積物の表面に、乾燥後に水不溶性となる溶
質を含む被覆用塗料、とくに野積堆積物と同一も
しくは類似する粉粒体を充填剤として加えてなる
上記塗料を塗工する方法がすでに提案されてい
る。 An excellent way to solve these problems is to
A method has already been proposed in which a coating material containing a solute that becomes water-insoluble after drying is applied to the surface of open deposits, in particular, the above-mentioned paint containing powder and granules that are the same as or similar to those of open deposits is added as a filler. ing.
この方法は極めて有効な方法であるが、野積堆
積物の含水率や粒度などの表面状態のばらつきお
よび塗工時の気温、湿度、天候などによつて形成
される塗膜の物性が変動し、また経日的に塗膜に
割れ、かけを生じ、防水、防塵などの効果に悪影
響を及ぼすことがあつた。 Although this method is extremely effective, the physical properties of the coating film formed vary depending on variations in surface conditions such as moisture content and particle size of the field deposits, as well as temperature, humidity, and weather at the time of coating. Moreover, the coating film cracked and chipped over time, which adversely affected the waterproofing, dustproofing, and other effects.
この発明者らは、上記の観点から鋭意検討を加
えた結果、野積堆積物の表面に被覆用塗料を塗装
する前に、特定の前処理剤を散布しておくと、上
記堆積物の表面状態や塗工時の気象条件のばらつ
きにもかかわらず、塗膜特性が安定して良質なも
のになることを見い出し、この発明をなすに至つ
た。 As a result of intensive studies from the above point of view, the inventors found that if a specific pre-treatment agent is sprayed on the surface of open deposits before coating the surface with coating paint, the surface condition of the deposits will improve. The inventors have discovered that the coating film properties are stable and of good quality despite variations in weather conditions during coating and coating, leading to the creation of this invention.
すなわち、この発明は、有効成分として一価ア
ルコール類、多価アルコールおよびその誘導体の
1種または2種以上を0.05重量%以上の濃度で含
む野積堆積物の被覆用前処理剤に係る第1の発明
と、上記の前処理剤を野積堆積物の表面に0.5〜
6Kg/m2の散布量で散布したのち、乾燥後に水溶
性となる溶質を含む被覆用塗料を塗装することを
特徴とする第2の発明とに係るものである。 That is, the present invention relates to a first pretreatment agent for coating field deposits containing one or more of monohydric alcohols, polyhydric alcohols, and their derivatives as an active ingredient at a concentration of 0.05% by weight or more. Invention, the above pretreatment agent is applied to the surface of open deposits at a rate of 0.5~
This invention relates to a second invention characterized in that, after being sprayed at a rate of 6 kg/m 2 , a coating paint containing a solute that becomes water-soluble after drying is applied.
この発明の前処理剤の有効成分である一価アル
コール類としては、メタノール、エタノール、n
―ブタノール、n―プロパノール、イソプロパノ
ール等が、多価アルコール類としては、プロピレ
ングリコール、ジプロピレングリコール、ポリエ
チレングリコール、エチレングリコール、ジエチ
レングリコール、トリエチレングリコール、ブタ
ンジオール、1・5―ペンタンジオール、グリセ
リン、ジグリセリン、トリメチロールプロパン等
が挙げられる。 The monohydric alcohols that are the active ingredients of the pretreatment agent of this invention include methanol, ethanol, n
-Butanol, n-propanol, isopropanol, etc.; polyhydric alcohols include propylene glycol, dipropylene glycol, polyethylene glycol, ethylene glycol, diethylene glycol, triethylene glycol, butanediol, 1,5-pentanediol, glycerin, dipropylene glycol, Examples include glycerin and trimethylolpropane.
また、多価アルコール類の誘導体としては、エ
チレングリコールモノメチルエーテル、エチレン
グリコールモノメチルエーテルアセテート、エチ
レングリコールモノエチルエーテル、エチレング
リコールジエチルエーテル、エチレングリコール
イソプロピルエーテル、エチレングリコールモノ
ブチルエーテル、エチレングリコールモノアセテ
ート、エチレングリコールジアセテート、ジエチ
レングリコールモノメチルエーテル、ジエチレン
グリコールモノエチルエーテル、ジエチレングリ
コールモノエチルエーテルアセテート、ジエチレ
ングリコールモノイソプロピルエーテル、ジエチ
レングリコールモノブチルエーテルなどがある。 In addition, as derivatives of polyhydric alcohols, ethylene glycol monomethyl ether, ethylene glycol monomethyl ether acetate, ethylene glycol monoethyl ether, ethylene glycol diethyl ether, ethylene glycol isopropyl ether, ethylene glycol monobutyl ether, ethylene glycol monoacetate, ethylene glycol Examples include diacetate, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monoethyl ether acetate, diethylene glycol monoisopropyl ether, and diethylene glycol monobutyl ether.
この発明の前処理剤は、水を代表例とする媒体
中に、上述の有効成分、とくに好適には一価アル
コール類および二価アルコール類のなかからその
1種もしくは2種以上を0.05重量%以上、好適に
は0.2〜2重量%の濃度で含ませてなるものであ
る。 The pretreatment agent of the present invention contains 0.05% by weight of the above-mentioned active ingredients, particularly preferably one or more of monohydric alcohols and dihydric alcohols, in a medium typically represented by water. As mentioned above, it is preferably contained at a concentration of 0.2 to 2% by weight.
この前処理剤には必要に応じてポリエステルポ
リオール、ポリエーテルポリオールの如き水溶性
ポリマーや、酢酸ビニルの重合体もしくはその共
重合体、アクリル酸エステルないしメタクリル酸
エステルの重合体もしくはそれらとスチレンとの
共重合体、ブタジエンとスチレンとの共重合体、
ブタジエンとアクリロニトリルとの共重合体など
の各種重合体のエマルジヨンを添加することがで
きる。 This pretreatment agent may include water-soluble polymers such as polyester polyols and polyether polyols, vinyl acetate polymers or copolymers thereof, acrylic ester or methacrylic ester polymers, or combinations thereof with styrene. Copolymer, copolymer of butadiene and styrene,
Emulsions of various polymers, such as copolymers of butadiene and acrylonitrile, can be added.
このような前処理剤によつて塗膜特性が安定化
する理由については必ずしも明らかではない。推
測では、野積堆積物の表面に前処理剤が吸着する
ことにより、塗料のぬれ性が改善されること、塗
料の造膜温度が下がり造膜しやすくなつてより強
い膜をつくること、さらに水溶性による堆積物表
面の締め固め効果などが考えられる。 The reason why coating film properties are stabilized by such pretreatment agents is not necessarily clear. It is speculated that the adsorption of the pretreatment agent on the surface of open deposits improves the wettability of the paint, lowers the film-forming temperature of the paint, makes it easier to form a film, and creates a stronger film, and that water-soluble This is thought to be due to the compaction effect of the sediment surface due to the soil temperature.
この発明の被覆方法は、まず上記の前処理剤
を、野積堆積物の表面に、0.5〜6Kg/m2の散布
量、とくに好ましくは2〜4Kg/m2の散布量で散
布する。このときの散布量が0.5Kg/m2未満では
野積堆積物の表面を十分にぬらすことができず、
6Kg/m2を超えると表面層の水分量が飽和となつ
て流動化した表面にクラツクが入つたり、山崩れ
の現象を招く。 In the coating method of the present invention, first, the above-mentioned pretreatment agent is sprayed onto the surface of the field deposit at an amount of 0.5 to 6 kg/m 2 , particularly preferably 2 to 4 kg/m 2 . If the amount of spraying at this time is less than 0.5Kg/ m2 , it will not be possible to wet the surface of the field deposits sufficiently.
If it exceeds 6 kg/m 2 , the water content in the surface layer becomes saturated, causing cracks to appear on the fluidized surface and the phenomenon of landslides.
散布方法は、スプレ、シヤワなどの噴霧散布が
望ましく、散布時に前処理剤が堆積物の表面を流
れおちることなく、十分浸透していくよう配慮す
る必要がある。 The preferred method of dispersion is spraying, showering, etc., and care must be taken during spraying to ensure that the pretreatment agent does not run off the surface of the deposit and is sufficiently permeated.
このように前処理剤を散布したのち、被覆用塗
料を約1〜10Kg/m2の割合で塗装する。この塗料
としてはその溶質が乾燥後に水不溶性となるもの
であれば従来公知のものを広く適用でき、水エマ
ルジヨン系および有機溶剤系のいずれでもよい。
とくに好ましい被覆用塗料は野積堆積物と同一も
しくは類似する材料からなる粉粒体を充填剤とし
て配合してなるものであり、この塗料は良好なチ
キソトロピー性を有しているため、堆積物内部へ
の浸透が抑えられて連続皮膜の形成に有利とな
る。 After spraying the pretreatment agent in this way, a coating paint is applied at a rate of about 1 to 10 kg/m 2 . As this paint, a wide range of conventionally known paints can be used as long as the solute becomes water-insoluble after drying, and it may be either a water emulsion type or an organic solvent type.
Particularly preferred coating paints are those that contain as a filler powder particles made of the same or similar material as the open deposits, and since this paint has good thixotropy, it does not penetrate into the interior of the deposits. permeation is suppressed, which is advantageous for the formation of a continuous film.
上記塗装によつて形成される塗膜は、前処理剤
の前記機能によつて野積堆積物の表面層の状態や
含水率などのばらつき、塗工時の気温、湿度、天
候などのばらつきに関係なく、常に安定した経日
的にも割れや裂けのみられない均一かつ連続した
膜特性を発揮する。 The coating film formed by the above coating is affected by variations in the condition and moisture content of the surface layer of open deposits, as well as variations in temperature, humidity, weather, etc. at the time of coating, depending on the function of the pretreatment agent. It exhibits uniform and continuous film properties without any cracks or tears even over time.
以上のように、この発明によれば、野積堆積物
の表面により信頼性の高い安定した良質の塗膜を
形成できるから、上記堆積物の防水、防塵、空気
による酸化防止などの効果を一段と高めることが
できる。 As described above, according to the present invention, it is possible to form a highly reliable, stable, and high-quality coating film on the surface of open deposits, thereby further enhancing the effects of waterproofing, dustproofing, and preventing oxidation by air of the deposits. be able to.
つぎに、この発明の実施例を記載する。 Next, examples of this invention will be described.
実施例 1
プロピレングリコールの0.3重量%水溶液を被
覆用前処理剤とした。この前処理剤を、床面積
4000m2、高さ15mの石炭粉からなる野積堆積物の
表面に、スプレで2Kg/m2散布した。翌日、下記
の組成からなる被覆用塗料を10Kg/m2塗工し、自
然乾燥させた。この方法で被覆した堆積物は6ケ
月経過しても崩壊することなく、この間石炭粉の
発塵や流失および含水比の変化は全く認められな
かつた。Example 1 A 0.3% by weight aqueous solution of propylene glycol was used as a pretreatment agent for coating. Apply this pretreatment agent to the floor area.
A spray of 2 kg/m 2 was applied to the surface of an open pile of coal powder measuring 4000 m 2 and 15 m high. The next day, 10 kg/m 2 of coating paint having the composition shown below was applied and allowed to air dry. The deposit coated with this method did not disintegrate even after 6 months had passed, and during this period no coal dust generation, no runoff, and no change in water content were observed.
<塗料組成>
アクリル酸ブチルとスチレンとの65/35の共
重合体の50重量%水
エマルジヨン 100容量部
エチルセロソルブ 2容量部
水 20容量部
5メツシユパスの石炭粉 1000容量部
実施例 2
メタノールとグリセリンとの重量比1対1の混
合物の10重量%水溶液を被覆用前処理剤とした。
この前処理剤を、床面積3600m2、高さ11mの石炭
粉からなる野積堆積物の表面に、スプレで4Kg/
m2散布した。約10時間後、実施例1で用いたと同
じ被覆用塗料を8Kg/m2塗工し、自然乾燥させ
た。この方法で被覆した堆積物は、6ケ月経過し
ても崩壊せず、この間石炭粉の発塵や流失および
含水比の変化は全く認められなかつた。<Paint composition> 50% by weight water emulsion of 65/35 copolymer of butyl acrylate and styrene 100 parts by volume Ethyl cellosolve 2 parts by volume Water 20 parts by volume 5 mesh pass coal powder 1000 parts by volume Example 2 Methanol and glycerin A 10% by weight aqueous solution of a mixture of 1:1 by weight was used as a pretreatment agent for coating.
This pretreatment agent was sprayed onto the surface of an open pile of coal powder with a floor area of 3,600 m 2 and a height of 11 m, at a rate of 4 kg/kg.
m 2 sprayed. After about 10 hours, 8 kg/m 2 of the same coating material as used in Example 1 was applied and allowed to air dry. The deposit coated with this method did not disintegrate even after 6 months had passed, and during this period no coal dust generation, no runoff, and no change in water content was observed.
比較例
床面積3000m2、高さ11mの石炭粉からなる野積
堆積物の表面に、前処理剤を施さず、実施例1で
用いたと同じ被覆用塗料を10Kg/m2塗工し、自然
乾燥させた。この方法で被覆した堆積物は6ケ月
経過の間に、石炭粉の発塵や流失はおこらなかつ
たものの、表面にクラツクが入り、石炭粉の含水
比が初期値の9重量%から10.5重量%迄上昇し
た。Comparative Example: On the surface of an open pile of coal powder with a floor area of 3000 m 2 and a height of 11 m, 10 kg/m 2 of the same coating paint used in Example 1 was applied without applying a pretreatment agent, and the mixture was air-dried. I let it happen. Although the deposit coated with this method did not generate dust or wash away after 6 months, cracks appeared on the surface and the moisture content of the coal powder increased from the initial value of 9% by weight to 10.5% by weight. rose to.
Claims (1)
コール類およびその誘導体の1種または2種以上
を0.05重量%以上の濃度で含む野積堆積物の被覆
用前処理剤。 2 野積堆積物の表面に、有効成分として一価ア
ルコール類、多価アルコール類およびその誘導体
の1種または2種以上を0.05重量%以上の濃度で
含む被覆用前処理剤を0.5〜6Kg/m2の散布量で
散布したのち、乾燥後に水不溶性となる溶質を含
む被覆用塗料を塗装することを特徴とする野積堆
積物の被覆方法。[Scope of Claims] 1. A pretreatment agent for coating field deposits containing one or more of monohydric alcohols, polyhydric alcohols, and derivatives thereof at a concentration of 0.05% by weight or more as an active ingredient. 2 Apply 0.5 to 6 kg/m of a coating pretreatment agent containing one or more of monohydric alcohols, polyhydric alcohols, and their derivatives as an active ingredient at a concentration of 0.05% by weight or more on the surface of open deposits. A method for covering open deposits, which comprises spraying the deposits at a rate of 2 and then applying a coating paint containing a solute that becomes water-insoluble after drying.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14525982A JPS5936007A (en) | 1982-08-20 | 1982-08-20 | Previous processing agent for covering and covering method for accumulation in open-air storage |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14525982A JPS5936007A (en) | 1982-08-20 | 1982-08-20 | Previous processing agent for covering and covering method for accumulation in open-air storage |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5936007A JPS5936007A (en) | 1984-02-28 |
JPS6116681B2 true JPS6116681B2 (en) | 1986-05-01 |
Family
ID=15380992
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14525982A Granted JPS5936007A (en) | 1982-08-20 | 1982-08-20 | Previous processing agent for covering and covering method for accumulation in open-air storage |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5936007A (en) |
-
1982
- 1982-08-20 JP JP14525982A patent/JPS5936007A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5936007A (en) | 1984-02-28 |
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