JPS6248B2 - - Google Patents
Info
- Publication number
- JPS6248B2 JPS6248B2 JP57145260A JP14526082A JPS6248B2 JP S6248 B2 JPS6248 B2 JP S6248B2 JP 57145260 A JP57145260 A JP 57145260A JP 14526082 A JP14526082 A JP 14526082A JP S6248 B2 JPS6248 B2 JP S6248B2
- Authority
- JP
- Japan
- Prior art keywords
- coating
- paint
- viscosity
- film
- deposit
- 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 36
- 239000011248 coating agent Substances 0.000 claims description 33
- 239000003973 paint Substances 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 10
- 238000001035 drying Methods 0.000 claims description 6
- 239000010408 film Substances 0.000 description 20
- 239000002344 surface layer Substances 0.000 description 11
- 239000013049 sediment Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000000843 powder Substances 0.000 description 9
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 8
- 229920001577 copolymer Polymers 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000000945 filler Substances 0.000 description 7
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 239000003245 coal Substances 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 239000000571 coke Substances 0.000 description 4
- 239000010419 fine particle Substances 0.000 description 4
- 239000004576 sand Substances 0.000 description 4
- 239000002562 thickening agent Substances 0.000 description 4
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 3
- 229920000180 alkyd Polymers 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 230000000149 penetrating effect Effects 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 230000008595 infiltration Effects 0.000 description 2
- 238000001764 infiltration Methods 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 235000010981 methylcellulose Nutrition 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-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
- NQBXSWAWVZHKBZ-UHFFFAOYSA-N 2-butoxyethyl acetate Chemical compound CCCCOCCOC(C)=O NQBXSWAWVZHKBZ-UHFFFAOYSA-N 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 229910001570 bauxite Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 1
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000007592 spray painting technique Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 239000008096 xylene Substances 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
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Paints Or Removers (AREA)
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装して堆積物の
防水、防塵、空気による酸化防止などを図るため
の被覆方法に関する。Detailed Description of the Invention This invention is a method of waterproofing deposits by coating the surface of the deposits when coal, coke, iron ore, minerals such as river sand, wood powder, etc. are deposited in open piles over a long period of time. , relates to a coating method for dustproofing, preventing oxidation due to air, etc.
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起して周辺地域
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
の原因となつたり、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。 Generally, coal, coke, wood powder, etc. are often stored in open piles at steel mills, gas plants, paper mills, etc. However, during storage, these sediments are easily stirred up by the wind, causing dust pollution in surrounding areas and causing sediment loss, and during rainfall, they flow into rivers and the sea, causing sewage. In addition, if the water content in deposits such as coal, coke, or iron ore becomes excessive, there are disadvantages such as evaporative heat loss of water when burning the deposits.
これらの問題を解決するすぐれた方法として、
堆積物の表面に堆積物と同一もしくは類似の粉粒
体を充填剤として配合した塗料を塗布することに
より乾燥後に水不溶性の塗膜を形成させる方法が
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 water-insoluble coating film is formed after drying by coating the surface of the deposit with a paint containing the same or similar powder as the deposit as a filler.
この方法においては塗料は大量の充填剤を含み
高粘度、チキソトロピツク性であつて、これが堆
積物内部に浸透してしまうことなく表面層に停ま
つた状態で乾燥固化し、防水、防塵性などの塗膜
を形成する。ここで、堆積物の表面は凹凸、疎密
の変化が大きいため、この上に連続した皮膜を形
成するためには大量の塗布が必要で、通常乾燥後
の塗膜厚は平均5mm以上に達する。 In this method, the paint contains a large amount of filler, is highly viscous, and has thixotropic properties, and it dries and solidifies while remaining on the surface layer without penetrating into the deposit, resulting in waterproof, dustproof, etc. Forms a coating film. Here, since the surface of the deposit has large irregularities and changes in density, a large amount of coating is required to form a continuous film thereon, and the average coating thickness after drying usually reaches 5 mm or more.
このため、単位要積当りの塗料コストが高くな
り、かつ高粘度のため塗装のランニングコストも
高くなる。また、膜厚が大きいため乾燥固化まで
の時間が、夏期で2日、冬期で4日以上かかり、
この間に降雨があつた場合塗膜の性能が著しく損
われるため、施行日程を天候に合わせて選ばなけ
ればならないなどの制約があつた。 For this reason, the paint cost per unit volume increases, and the running cost of painting also increases due to the high viscosity. In addition, due to the large thickness of the film, it takes two days to dry and solidify in the summer and more than four days in the winter.
If it rained during this period, the performance of the paint film would be significantly impaired, so there were restrictions such as the installation schedule having to be chosen according to the weather.
一方、この発明者らは、上記塗膜の防水性、防
塵性などは実質的に塗膜のごく表面の薄膜部分の
みで十分果されることを見い出したが、現実には
塗装量を減らして塗膜を薄くすると連続皮膜が形
成されず、やむもえず前記欠点のある厚塗りを行
なつていた。 On the other hand, the inventors discovered that the waterproof and dustproof properties of the above-mentioned coating film are substantially achieved only by a thin film on the very surface of the coating film, but in reality, it is necessary to reduce the amount of coating. When the coating film is made thinner, a continuous coating cannot be formed, and thick coatings with the above-mentioned drawbacks are unavoidable.
この発明者らは、このような問題の解決のため
に鋭意研究を続けた結果、塗料の粘度を特定の低
粘度範囲に調整し、かつ塗装量を特定範囲内に限
定した場合、堆積物表面層にある堆積物微粒子が
適度に流動し堆積物の表面の疎な部分に至つて沈
降する、いわゆる目詰め効果を生じ、これが堆積
物表面への極めて薄い連続皮膜の形成に好結果を
与えるものであることを見い出し、この発明をな
すに至つた。 As a result of intensive research to solve these problems, the inventors found that when the viscosity of the paint was adjusted to a specific low viscosity range and the amount of paint was limited to a specific range, deposits on the surface The fine sediment particles in the layer flow moderately and settle down to the sparse parts of the sediment surface, creating a so-called clogging effect, which results in the formation of an extremely thin continuous film on the sediment surface. They discovered that this is the case and came up with this invention.
すなわち、この発明は、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を塗
装するに際して、塗料粘度を5〜500センチポイ
ズに調整すると共に、塗装量を1〜5Kg/m2に設
定したことを特徴とする野積堆積物の被覆方法に
係るものである。 That is, when applying a coating paint containing a solute that becomes water-insoluble after drying to the surface of field deposits, the present invention adjusts the viscosity of the paint to 5 to 500 centipoise, and adjusts the coating amount to 1 to 5 kg/ m2. The present invention relates to a method for covering open deposits, characterized in that the method is set as follows.
この発明に適用される野積堆積物とは、たとえ
ば石炭(粉)、コークス(粉)、鉄鉱石、川砂のよ
うな鉱物、銅鉱石、石灰岩、ボーキサイトその他
の金属鉱石または木粉などの有機粉末物などであ
る。 The open deposits applied to this invention are, for example, coal (powder), coke (powder), iron ore, minerals such as river sand, copper ore, limestone, bauxite and other metal ores, or organic powders such as wood powder. etc.
この発明において被覆用塗料とは、乾燥後に水
不溶性となる溶質を含むものであつて、水エマル
ジヨン系のものが好適であるが、有機溶媒系であ
つてもさしつかえない。水エマルジヨン系塗料の
場合、造膜助剤、増粘剤、消泡剤、凍解安定剤な
どの任意成分の添加が可能である。とりわけ増粘
剤は以下に述べる粘度の調節に重要であり、その
選択は十分配慮されなければならない。 In this invention, the coating material contains a solute that becomes water-insoluble after drying, and is preferably a water emulsion type, but an organic solvent type may also be used. In the case of a water emulsion paint, optional components such as a film-forming agent, a thickener, an antifoaming agent, and a freeze-thaw stabilizer can be added. In particular, the thickener is important for adjusting the viscosity described below, and its selection must be carefully considered.
塗料固形分の主材となる樹脂の代表例を挙げれ
ば、水エマルジヨン系では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、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
合体などがあり、また有機溶剤系ではスチレン化
アルキツド、キシレン樹脂変性アルキツド、塩化
ビニルと酢酸ビニルとの共重合体などがある。 Typical examples of resins that are the main component of paint solids include vinyl acetate polymers or their copolymers, acrylic acid ester, methacrylic acid ester polymers, or their copolymers with styrene in water emulsion systems. , copolymers of butadiene and styrene, copolymers of butadiene and acrylonitrile, and organic solvent-based alkyds such as styrenated alkyds, xylene resin-modified alkyds, and copolymers of vinyl chloride and vinyl acetate.
水エマルジヨン系塗料に通常添加される造膜助
剤と増粘剤とにつきその具体例を挙げると、造膜
助剤としてはブチルセロソルブ、ブチルカルビト
ール、ブチルセルソルブアセテート、カルビトー
ルアセテート、ヘキシレングリコール、ジブチル
フタレート、ジオクチルフタレートなどがあり、
増粘剤としてはメチルセルロース、エチルセルロ
ース、ポリビニルアルコール、ヒドロキシエチル
セルロース、カルボキシメチルセルロース、ポリ
アクリル酸ソーダ、カゼイン、デンプンなどがあ
る。 Specific examples of film forming aids and thickeners that are usually added to water emulsion paints include butyl cellosolve, butyl carbitol, butyl cellosolve acetate, carbitol acetate, and hexylene glycol. , dibutyl phthalate, dioctyl phthalate, etc.
Thickeners include methylcellulose, ethylcellulose, polyvinyl alcohol, hydroxyethylcellulose, carboxymethylcellulose, sodium polyacrylate, casein, and starch.
この発明においては上記の塗料を野積堆積物の
表面に塗装するに際して、その粘度を5〜500セ
ンチポイズ、好ましくは10〜100センチポイズに
調整し、かつ塗装量を1〜5Kg/m2、好ましくは
2〜3Kg/m2とすることが特に重要である。この
条件を満たして塗装した場、野積堆積物の表面層
には極めて薄い均一連続皮膜が形成され、かつそ
の皮膜は十分な防水性、防塵性、酸化防止性を有
する。 In this invention, when applying the above-mentioned paint to the surface of open deposits, the viscosity is adjusted to 5 to 500 centipoise, preferably 10 to 100 centipoise, and the coating amount is 1 to 5 kg/m 2 , preferably 2. It is particularly important to set it to ~3Kg/ m2 . When this condition is met and the coating is applied, an extremely thin uniform continuous film is formed on the surface layer of the field deposit, and the film has sufficient waterproof, dustproof, and antioxidant properties.
このような効果はおよそ次のようなメカニズム
によるものと考えられる。塗料が塗布された堆積
物の表面層において、表面層中の大きな堆積物粒
子は動かないが、微粒子は塗料の流れに沿つて流
動し、堆積物表面を浮遊移動して表面層の疎な部
分(大きな堆積物粒子の集合部)に至ると、塗料
は停滞し微粒子は沈降する。その結果、表面層は
日詰りを生じ全面が緻密な層となる。塗料は適度
な粘性を保つているため、簡単に堆積物中に浸透
してしまうことはないが、上記微粒子の目詰め効
果によつて一層内部へ浸透しにくくなり、表面層
に停まつたまま乾燥固化する。このため、堆積物
は本来極めて疎な表面層を有しており、また塗料
は極めて低粘度であるにもかかわらず、塗料が内
部に浸透してしまうことなく、表面層に停まり極
めて効率よく連続塗膜を形成する。 This effect is thought to be due to the following mechanism. In the surface layer of a deposit coated with paint, large sediment particles in the surface layer do not move, but fine particles flow along with the flow of the paint, floating on the sediment surface and spreading to sparse areas of the surface layer. When reaching a point (where large sediment particles gather), the paint stagnates and the fine particles settle. As a result, the surface layer becomes clogged and the entire surface becomes a dense layer. Since the paint maintains an appropriate viscosity, it does not easily penetrate into the deposit, but the clogging effect of the fine particles mentioned above makes it even more difficult for it to penetrate inside, and it remains stuck on the surface layer. Dry and solidify. For this reason, deposits originally have an extremely sparse surface layer, and even though paint has an extremely low viscosity, the paint remains in the surface layer without penetrating into the interior, making it extremely efficient. Forms a continuous coating.
塗料の粘度が5センチポイズ未満の場合、塗料
は速やかに堆積物中に浸透し、微粒子の流動を生
じるに至らず、従つて目詰め効果を生じない。ま
た500センチポイズを超えると微粒子の流動は粘
性によつて抑制されるためやはり目詰め効果を生
じるに至らない。塗装量が1Kg/m2未満では堆積
物微粒子を浮遊移動させるに十分な流動性を生じ
ず、5Kg/m2を超えると堆積物の表面層が塗料で
飽和され、地すべり、山崩れ現象を生じてしま
う。 When the viscosity of the paint is less than 5 centipoise, the paint penetrates quickly into the deposit and does not lead to particulate flow and therefore no plugging effect. Moreover, if the particle diameter exceeds 500 centipoise, the flow of fine particles is suppressed by viscosity, so that no clogging effect is produced. If the amount of coating is less than 1 kg/m 2 , sufficient fluidity will not be created to float and move sediment particles, and if it exceeds 5 kg/m 2 , the surface layer of the sediment will be saturated with paint, causing landslides and landslides. Put it away.
このメカニズムから、あらかじめ被覆用塗料中
に充填剤を混合して、塗装時に上記充填剤の流動
性により前記同様の目詰め効果を生じさせること
が期待される。事実、堆積物の表面層に微粒子が
少ない場合などはかかる充填剤の使用は好ましい
結果を与える。ただし、この場合、塗料の粘度が
高くなるため希釈によつて粘度を下げなければな
らない。しかし、粘度低下と共に充填剤が沈降す
るなどの弊害を伴うので注意が必要である。また
充填剤によつては、堆積物中への混入が好ましく
ないものもあり、一般には堆積物と同一もしくは
類似の材料を用いることが望ましい。 Based on this mechanism, it is expected that by mixing a filler into the coating paint in advance, the fluidity of the filler will produce the same plugging effect as described above during coating. In fact, the use of such fillers gives favorable results, such as when the surface layer of the deposit is low in particulates. However, in this case, the viscosity of the paint increases, so the viscosity must be lowered by dilution. However, care must be taken because this method has disadvantages such as sedimentation of the filler along with a decrease in viscosity. Furthermore, some fillers are undesirable if mixed into the deposit, and it is generally desirable to use a material that is the same as or similar to the deposit.
この発明において塗装方法としては、吹きつけ
塗装、流し塗りなどの方法を採用でき、この塗装
後通常は自然乾燥させればよい。この間、塗装さ
れた前記塗料は目詰め効果によりほとんど内部へ
浸入することなく表面に停まるため、その乾燥が
早くかつ均一連続の皮膜を形成する。 In the present invention, spray coating, flow coating, or other methods can be used as the coating method, and after this coating, it is usually sufficient to allow the coating to dry naturally. During this time, the applied paint stays on the surface without penetrating into the interior due to the packing effect, so it dries quickly and forms a uniform and continuous film.
以上、詳述したとおり、この発明によれば、用
いる塗料が低粘度のため塗装ランニングコストを
低下でき、また膜厚が薄いため単位面績当たりの
塗料コストを低くできる。さらに乾燥固化までの
時間を短縮できるため、施行が天候によつてそれ
ほど左右されることがないなどの利点が得られ
る。 As detailed above, according to the present invention, since the paint used has a low viscosity, the running cost of the coating can be reduced, and since the film thickness is thin, the paint cost per unit area can be reduced. Furthermore, since the time required for drying and solidification can be shortened, there are advantages such as the fact that the application process is not so dependent on the weather.
つぎに、この発明の実施例につき説明する。 Next, embodiments of this invention will be described.
実施例 1
単量体組成が65:35のアクリル酸ブチルとスチ
レンとの共重合体の50重量%水エマルジヨン100
容量部、ポリアクリル酸ソーダの2重量%水溶液
12容量部、ブチルセロソルブ2容量部およびヘキ
サメタリン酸ソーダの10重量%水溶液0.8容量部
に、水885容量部を加えて、粘度20センチポイズ
の被覆用塗料とした。Example 1 50% by weight water emulsion 100 of a copolymer of butyl acrylate and styrene with a monomer composition of 65:35
Part by volume, 2% by weight aqueous solution of sodium polyacrylate
12 parts by volume of butyl cellosolve, 2 parts by volume of butyl cellosolve, and 0.8 parts by volume of a 10% by weight aqueous solution of sodium hexametaphosphate were added with 885 parts by volume of water to prepare a coating material with a viscosity of 20 centipoise.
この塗料を用いて、床面積4000m2、高さ15mの
石炭粉よりなる野積堆積物の表面に3Kg/m2見当
の吹きつけ塗装を行なつた。塗膜は5時間後にほ
ぼ乾燥固化した。膜厚は約0.5mmであつた。 Using this paint, the surface of an open pile of coal powder with a floor area of 4000 m 2 and a height of 15 m was sprayed at a target of 3 kg/m 2 . The coating film was almost dry and solidified after 5 hours. The film thickness was approximately 0.5 mm.
このようにして被覆した堆積物は、6ケ月経過
しても崩壊せず、石炭粉の飛散や流出、雨水の浸
入は全く認められなかつた。 The deposit coated in this manner did not disintegrate even after 6 months had passed, and no scattering or runoff of coal powder or infiltration of rainwater was observed.
実施例 2
単量体組成が50:50のスチレンとブタジエンの
共重合体の48重量%ラテツクス100容量部、セロ
ソルブアセテート3容量部、メチルセルロース2
重量%水溶液25容量部および10メツシユパスの川
砂100重量部に、水225容量部を加えて粘度60セン
チポイズ、固形分濃度33重量%の被覆用塗料とし
た。Example 2 100 parts by volume of 48% by weight latex of a copolymer of styrene and butadiene with a monomer composition of 50:50, 3 parts by volume of cellosolve acetate, 2 parts by volume of methyl cellulose
225 parts by volume of water was added to 25 parts by volume of a wt% aqueous solution and 100 parts by weight of river sand of 10 mesh passes to prepare a coating paint having a viscosity of 60 centipoise and a solid content concentration of 33 wt%.
この塗料を、床面績240m2、高さ6mの川砂か
らなる野積堆積物の表面に2Kg/m2流し塗りし
た。塗膜は8時間後にはほぼ乾燥固化した。膜厚
は約1.5mmであつた。 This paint was poured at 2 kg/m 2 onto the surface of an open pile of river sand with a floor area of 240 m 2 and a height of 6 m. The coating film was almost dry and solidified after 8 hours. The film thickness was approximately 1.5 mm.
このようにして被覆した堆積物は、6カ月経過
しても崩壊せず、飛散や流出、雨水の浸入は認め
られなかつた。 The deposit coated in this manner did not disintegrate even after 6 months had passed, and no scattering, runoff, or infiltration of rainwater was observed.
比較例
水量を300容量部とした以外は、実施例1と同
様の配合組成からなる粘度600センチポイズの被
覆用塗料とした。この塗料を用いて、実施例1と
同じ堆積物の表面に4Kg/m2見当の吹きつけ塗装
を行なつた。塗膜は3日後に乾燥固化した。膜厚
は約4mmであつた。Comparative Example A coating paint having a viscosity of 600 centipoise was prepared, having the same composition as in Example 1 except that the amount of water was 300 parts by volume. Using this paint, spray painting was performed on the surface of the same deposit as in Example 1 at a target of 4 kg/m 2 . The coating film dried and solidified after 3 days. The film thickness was approximately 4 mm.
この方法で、被覆した堆積物は、3カ月後に塗
膜にクラツクが入りはじめ、含水率の上昇が認め
られた。 After three months, cracks began to appear in the coated deposits coated with this method, and an increase in moisture content was observed.
Claims (1)
溶質を含む被覆用塗料を塗装するに当たり、上記
塗料の粘度を5〜500センチポイズに調整すると
共に、塗装量を1〜5Kg/m2に設定したことを特
徴とする野積堆積物の被覆方法。1. When coating the surface of open deposits with a coating paint containing a solute that becomes water-insoluble after drying, the viscosity of the paint was adjusted to 5 to 500 centipoise, and the coating amount was set to 1 to 5 kg/ m2. A method for covering open deposits, characterized by:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14526082A JPS5936008A (en) | 1982-08-20 | 1982-08-20 | Method of covering accumulation in open-air storage |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14526082A JPS5936008A (en) | 1982-08-20 | 1982-08-20 | Method of covering accumulation in open-air storage |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5936008A JPS5936008A (en) | 1984-02-28 |
JPS6248B2 true JPS6248B2 (en) | 1987-01-06 |
Family
ID=15381012
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14526082A Granted JPS5936008A (en) | 1982-08-20 | 1982-08-20 | Method of covering accumulation in open-air storage |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5936008A (en) |
-
1982
- 1982-08-20 JP JP14526082A patent/JPS5936008A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5936008A (en) | 1984-02-28 |
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