JPS6129787B2 - - Google Patents
Info
- Publication number
- JPS6129787B2 JPS6129787B2 JP16351978A JP16351978A JPS6129787B2 JP S6129787 B2 JPS6129787 B2 JP S6129787B2 JP 16351978 A JP16351978 A JP 16351978A JP 16351978 A JP16351978 A JP 16351978A JP S6129787 B2 JPS6129787 B2 JP S6129787B2
- Authority
- JP
- Japan
- Prior art keywords
- hot melt
- melt adhesive
- granular aggregate
- coated
- plate
- 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
- 239000004831 Hot glue Substances 0.000 claims description 23
- 238000000034 method Methods 0.000 claims description 20
- 238000010438 heat treatment Methods 0.000 claims description 10
- 238000002844 melting Methods 0.000 claims description 7
- 230000008018 melting Effects 0.000 claims description 7
- 229920005989 resin Polymers 0.000 description 16
- 239000011347 resin Substances 0.000 description 16
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 8
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 229910000019 calcium carbonate Inorganic materials 0.000 description 4
- 239000004568 cement Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000003973 paint Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 3
- 239000010425 asbestos Substances 0.000 description 3
- 239000000378 calcium silicate Substances 0.000 description 3
- 229910052918 calcium silicate Inorganic materials 0.000 description 3
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229910052895 riebeckite Inorganic materials 0.000 description 3
- 239000004576 sand Substances 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000012943 hotmelt Substances 0.000 description 2
- 239000011256 inorganic filler Substances 0.000 description 2
- 229910003475 inorganic filler Inorganic materials 0.000 description 2
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 2
- 239000001095 magnesium carbonate Substances 0.000 description 2
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000011120 plywood Substances 0.000 description 2
- 229920006122 polyamide resin Polymers 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 108010039491 Ricin Proteins 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 238000009435 building construction Methods 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000011094 fiberboard Substances 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 150000003097 polyterpenes Chemical class 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 239000010454 slate Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
Description
【発明の詳細な説明】
本発明は被塗装板表面に迅速かつ経済的に砂状
模様を形成する方法である。DETAILED DESCRIPTION OF THE INVENTION The present invention is a method for quickly and economically forming a sandy pattern on the surface of a plate to be coated.
従来、工場塗装において、成形板に砂状模様
(リシン仕上げ)を施す方法として(1)一般的な建
造物工事現場等で行なわれているような粒状骨材
が混入された塗料をスプレーガン等を用いて成形
板に塗装し加熱乾燥させる方法(2)成形板に、接着
材または塗料をロールコーター等を用いて均一に
塗装し、それが固化しない前に粒状骨材を散布し
たのち、カーテンフローコーター等を使用してさ
らにその上から塗料を塗布せしめ加熱乾燥させる
方法等がある。 Traditionally, in factory painting, the method of applying a sand-like pattern (resin finish) to a molded board is as follows: (1) Paint mixed with granular aggregate, which is used at general building construction sites, is applied with a spray gun, etc. Method of coating the molded board using a roller coater and drying by heating. There is a method of further applying a paint on top of the coating using a flow coater and drying it by heating.
しかしながら、(1)の方法では塗膜の厚さが必要
以上に大きくなるのみで無く、塗料の歩留が悪く
経済的な難点がある。(2)の方法では工程数が多く
それらの装置の維持管理に労力を要する欠陥があ
つた。その上、従来の方法では、塗料を固化また
は、硬化させるために加熱乾燥を行なわなければ
ならず、塗料中に含まれる大量の有機溶剤が大気
中に揮散し臭気、大気汚染の原因になりうる可能
性があつた。 However, in method (1), not only the thickness of the coating film becomes larger than necessary, but also the yield of the coating material is poor and there are economical drawbacks. Method (2) had a defect in that it required a large number of steps and required labor to maintain and manage the equipment. Furthermore, in conventional methods, the paint must be heated and dried in order to solidify or harden, and large amounts of organic solvents contained in the paint can volatilize into the atmosphere, causing odor and air pollution. There was a possibility.
本発明は、上記の欠点を解消するために発明さ
れた方法であると共に安価で生産性を大幅に向上
させて砂状模様の形成方法を提供することが出来
るものである。 The present invention is a method invented to eliminate the above-mentioned drawbacks, and can provide a method for forming a sand-like pattern at low cost and with greatly improved productivity.
すなわち、本発明はホツトメルト接着材によつ
て被覆された粒状骨材を、被塗装板上に散布せし
めたのちに加熱し、ホツトメルト接着材の熔融に
より該粒状骨材を被塗装板表面に固着させること
を特徴とする砂状模様の形成方法であり、またホ
ツトメルト接着材によつて被覆された粒状骨材を
既に加熱された被塗装板上に散布せしめ、該粒状
骨材をホツトメルト接着材の熔融により被塗装板
表面に固着させることを特徴とする砂状模様の形
成方法である。 That is, in the present invention, granular aggregate coated with a hot melt adhesive is spread on a plate to be painted, and then heated, and the granular aggregate is fixed to the surface of the plate to be painted by melting the hot melt adhesive. This method of forming a sand-like pattern is characterized by: scattering granular aggregate coated with a hot melt adhesive onto an already heated plate to be coated; This is a method for forming a sand-like pattern, which is characterized by fixing it to the surface of a plate to be coated.
本発明の基本的構成はベニヤ板、炭酸マグネシ
ウム板、硅酸カルシウム板、炭酸カルシウム板、
アスベストセメント板、木片セメント板等、建造
物の内外装に使用される成形板に迅速かつ経済的
に砂状模様(リシン仕上げ)を施す方法に関する
ものであり、重要な構成は有機溶剤などの揮発性
成分または水などの蒸発性成分が含有されていな
い着色または透明なホツトメルト接着材によつて
被覆された粒状骨材をもちいること、該粒状骨材
を被塗装板表面上に散布し、次の加熱工程によつ
て粒状骨材に被覆されたホツトメルト接着材を熔
融させ、熔融されたホツトメルト接着材により被
塗装板表面に粒状骨材を固着し砂状模様を形成す
ることである。 The basic structure of the present invention is a plywood board, a magnesium carbonate board, a calcium silicate board, a calcium carbonate board,
It concerns a method for quickly and economically applying a sand-like pattern (resin finish) to molded boards used for the interior and exterior of buildings, such as asbestos cement boards and wood chip cement boards, and the important component is the evaporation of organic solvents. The use of granular aggregate coated with a colored or transparent hot melt adhesive that does not contain volatile components or evaporable components such as water, and the use of granular aggregate coated with a colored or transparent hot melt adhesive that does not contain volatile components or evaporative components such as water; The heating process melts the hot melt adhesive coated on the granular aggregate, and the molten hot melt adhesive adheres the granular aggregate to the surface of the plate to be coated to form a sand-like pattern.
茲に本発明の方法を以下詳細に説明する。 The method of the present invention will now be described in detail.
さて粒状骨材は限定されるものではないが、寒
水砂、硅砂、各種鉱物の粉砕物、合成骨材陶磁器
類の粉砕物等が使用できる。勿論前記の二種以上
の混合併用も可能である。また、その大きさや形
状及び粒度分布も限定されるものではない。 The granular aggregate is not limited, but can be used, such as cold water sand, silica sand, pulverized products of various minerals, and pulverized products of synthetic aggregate ceramics. Of course, it is also possible to mix and use two or more of the above. Moreover, the size, shape, and particle size distribution are not limited either.
ホツトメルト接着材は、熱可塑性樹脂のみでも
よいが、その他に改質材として粘着付与樹脂、軟
化剤、無機の充填材、着色剤及び安定剤等が添加
剤として使用する。 The hot melt adhesive may be made of only a thermoplastic resin, but other modifiers such as a tackifying resin, a softener, an inorganic filler, a coloring agent, a stabilizer, and the like are used as additives.
熱可塑性樹脂としてはポリウレタン樹脂、ポリ
アミド樹脂、酢酸ビニール樹脂、アクリル系樹
脂、エポキシ樹脂、合成ゴム系樹脂、塩化ビニル
系樹脂、オレフイン系樹脂、ポリエステルル系樹
脂等でこれらの二種以上の共重合物であつても、
差支えない。 Thermoplastic resins include polyurethane resins, polyamide resins, vinyl acetate resins, acrylic resins, epoxy resins, synthetic rubber resins, vinyl chloride resins, olefin resins, polyester resins, and copolymerization of two or more of these resins. Even if it is a thing,
No problem.
粘着付与樹脂としては、クマロン樹脂、インデ
ン樹脂、ポリテルペン樹脂、ロジン、石油樹脂、
スチレン樹脂等であり、軟化剤には、フタル酸エ
ステル、リン酸エステル、パラフイン等がある。 Tackifying resins include coumarone resin, indene resin, polyterpene resin, rosin, petroleum resin,
Styrene resin, etc., and softeners include phthalate esters, phosphate esters, paraffin, etc.
無機の充填剤としては酸化チタン、亜鉛華、酸
化マグネシウム、水酸化アルミ、炭酸カルシウ
ム、硅石粉等がある。 Examples of inorganic fillers include titanium oxide, zinc white, magnesium oxide, aluminum hydroxide, calcium carbonate, and silica powder.
これらの例示は本発明を限定するものではな
い。また、上記のものは1種または2種以上を混
合物として使用できる。 These examples are not intended to limit the invention. Moreover, the above-mentioned ones can be used alone or as a mixture of two or more.
本発明の方法に用いるホツトメルト接着材の融
点は特に限定されるものではないが、好ましくは
50℃以上が良い。50℃以下では、加工された被塗
装板の砂状模様が通常の使用状態において熱変形
を起す恐れがある。 The melting point of the hot melt adhesive used in the method of the present invention is not particularly limited, but preferably
A temperature of 50℃ or higher is best. At temperatures below 50°C, there is a risk that the sand-like pattern on the processed plate to be coated may undergo thermal deformation under normal usage conditions.
被塗装板は、ホツトメルト樹脂材の融点温度で
変性または変形しないものであれば、いかなるも
のでもよい。例示すれば、合板、石膏ボード、石
綿セメント板、パーテイクルボード、プラスチツ
ク板、繊維板、炭酸マグネシウム板、炭酸カルシ
ウム板、硅酸カルシウム板、木片セメント板、等
である。 The plate to be coated may be of any type as long as it does not denature or deform at the melting point temperature of the hot melt resin material. Examples include plywood, gypsum board, asbestos cement board, particle board, plastic board, fiberboard, magnesium carbonate board, calcium carbonate board, calcium silicate board, wood chip cement board, and the like.
ホツトメルト接着材の配合方法は押出機等を用
いて熱熔融撹拌混合を行ない製造されるが、それ
を粒状骨材に被覆する方法としては、粒状骨材と
ホツトメルト接着材を熔融撹拌混合した後でロー
タリーキルンに導き、取り出し口付近の温度をホ
ツトメルト接着材の軟化点温度以下に調整してお
けば、保有温度が低下して各粒の粒状骨材のまわ
りに均一に付着されたものを得ることができる。 The method of compounding hot melt adhesive is to perform hot melt stirring mixing using an extruder etc., but the method of coating it on granular aggregate is after mixing the granular aggregate and hot melt adhesive by melting and stirring. By introducing the hot melt adhesive into the rotary kiln and adjusting the temperature near the outlet to below the softening point temperature of the hot melt adhesive, the holding temperature will be lowered and it will be possible to obtain aggregates that are evenly adhered around each grain of granular aggregate. can.
また、粒状骨材のまわりにホツトメルト接着材
を付着させる他の方法としては、粒状骨材とホツ
トメルト接着材とを混合共存させて加熱によりホ
ツトメルト接着材を熔融し、その後冷却して粒状
骨材を包含するホツトメルト接着材の塊状物を生
成し、その塊状物を適当粒度に粉砕した後に所定
粒度に分級調整することである。 Another method for attaching hot melt adhesive around granular aggregate is to mix and coexist the granular aggregate and hot melt adhesive, melt the hot melt adhesive by heating, and then cool the granular aggregate. The process involves producing a lump of hot melt adhesive, pulverizing the lump to a suitable particle size, and then classifying it to a predetermined particle size.
被塗装板に該粒状骨材を散布する方法は、振動
フルイを用いるか、該粒状骨材を入れるためのホ
ツパー底部に、底部開口面に沿つて回転する。多
数の透孔が穿設された有孔円筒を装備する装置を
用いてもよい。 The method of dispersing the granular aggregate onto the plate to be coated is by using a vibrating sieve or by rotating the hopper at the bottom of the hopper for receiving the granular aggregate along the bottom opening surface. It is also possible to use a device equipped with a perforated cylinder with a large number of through holes.
被塗装板の表面温度が粒状骨材を散布する際
に、被覆されたホツトメルト接着材の融点以上
(好ましくはそれよりも10℃以上高めが良い)に
あらかじめ加熱されていれば、砂状模様は散布終
了と同時に完成されるが、被塗装板の表面温度が
それ以下の場合は粒状骨材の散布後加熱工程が必
要となる。 If the surface temperature of the plate to be coated is preheated to a temperature higher than the melting point of the coated hot melt adhesive (preferably at least 10°C higher than that) when the granular aggregate is spread, the sandy pattern will be removed. It is completed at the same time as the spraying is finished, but if the surface temperature of the plate to be coated is below that temperature, a heating step is required after the granular aggregate is spread.
この加熱の炉内条件は加熱時間と加熱温度によ
つて主に規定され、粒状骨材に被覆されたホツト
メルト接着材が熔融するに必要な熱エネルギーを
与えてやらなければならない。 The furnace conditions for this heating are mainly determined by the heating time and heating temperature, and it is necessary to provide the necessary thermal energy to melt the hot melt adhesive coated on the granular aggregate.
茲に実施例によつて説明する。 This will be explained in detail using an example.
実施例 1
エチレン酢ビ樹脂50重量部、クマロン樹脂20重
量部、酸化チタン10重量部、炭酸カルシウム20重
量部をブレンダーで充分撹拌混合した後押し出し
機をもちいて加熱熔融混練をする。Example 1 50 parts by weight of ethylene vinyl acetate resin, 20 parts by weight of Coumaron resin, 10 parts by weight of titanium oxide, and 20 parts by weight of calcium carbonate were sufficiently stirred and mixed in a blender and then heated and melted and kneaded using a booster.
その混練物100重量部をホツトブレンダーに入
れて、その中に寒水石の5厘目を200重量部加え
加熱熔融撹拌する。それが冷えない内にロータリ
ーキルンに投入し30分間滞留させる。ロータリー
キルンは入口温度250℃取り出し口温度30℃に設
定してある。 Put 100 parts by weight of the kneaded product into a hot blender, and add 200 parts by weight of the 5th ring of Kansuiseki into the mixture and heat to melt and stir. Before it gets cold, it is put into a rotary kiln and left there for 30 minutes. The rotary kiln is set at an inlet temperature of 250°C and an outlet temperature of 30°C.
次に厚さ9m/mの石綿スレート板に振動フル
イを用いて上記の粒状骨材物を散布した後、熱風
循環式乾燥機を使用して、150℃5分間加熱した
後に取り出したところ、リシン模様を有する化粧
板を得ることが出来た。 Next, the above granular aggregate was spread on an asbestos slate board with a thickness of 9 m/m using a vibrating sieve, and then heated at 150°C for 5 minutes using a hot air circulation dryer and then taken out. A decorative board with a pattern could be obtained.
実施例 2
ポリアミド樹脂60重量部、石油樹脂30重量部、
パラフイン10重量部をブレンダーで充分撹拌混合
した後、押し出し機をもちいて加熱熔融混練をす
る。Example 2 60 parts by weight of polyamide resin, 30 parts by weight of petroleum resin,
After sufficiently stirring and mixing 10 parts by weight of paraffin in a blender, the mixture is heated and melted and kneaded using an extruder.
その混練物100重量部をホツトブレンダーに入
れてその中に硅砂の3号を200重量部加え、加熱
しながら熔融撹拌し、それが冷えない間にロータ
リーキルンに投入し30分間滞留させる。ロータリ
ーキルンは入口温度250℃、取り出し口温度30℃
に設定してある。 Put 100 parts by weight of the kneaded product into a hot blender, add 200 parts by weight of No. 3 silica sand, melt and stir while heating, and while the mixture is still cool, put it into a rotary kiln and leave it there for 30 minutes. The rotary kiln has an inlet temperature of 250℃ and an outlet temperature of 30℃.
It is set to .
次いで、前加熱によつて表面温度が110℃に予
熱された硅酸カルシウム板上に振動フルイを用い
て上記粒状骨材を散布したあと自然冷却したとこ
ろリシン模様を有する化粧板を得ることが出来
た。 Next, the above granular aggregate was spread using a vibrating sieve onto a calcium silicate board whose surface temperature had been preheated to 110°C, and then allowed to cool naturally, yielding a decorative board with a ricin pattern. Ta.
Claims (1)
骨材を被塗装板上に散布せしめたのちに加熱し、
ホツトメルト接着材の熔融により該粒状骨材を被
塗装板表面に固着させることを特徴とする砂状模
様の形成方法。 2 ホツトメルト接着材によつて被覆された粒状
骨材を既に加熱された被塗装板上に散布せしめ、
該粒状骨材をホツトメルト接着材の熔融により被
塗装板表面に固着させることを特徴とする砂状模
様の形成方法。[Claims] 1. Sprinkling granular aggregate coated with a hot melt adhesive onto a plate to be coated and then heating it;
A method for forming a sand-like pattern, which comprises fixing the granular aggregate to the surface of a plate to be painted by melting a hot melt adhesive. 2 Spreading the granular aggregate coated with hot melt adhesive onto the already heated plate to be coated,
A method for forming a sand-like pattern, which comprises fixing the granular aggregate to the surface of a plate to be painted by melting a hot melt adhesive.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16351978A JPS5586566A (en) | 1978-12-25 | 1978-12-25 | Method of making sandlike pattern |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16351978A JPS5586566A (en) | 1978-12-25 | 1978-12-25 | Method of making sandlike pattern |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5586566A JPS5586566A (en) | 1980-06-30 |
JPS6129787B2 true JPS6129787B2 (en) | 1986-07-09 |
Family
ID=15775401
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16351978A Granted JPS5586566A (en) | 1978-12-25 | 1978-12-25 | Method of making sandlike pattern |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5586566A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5611215A (en) * | 1979-07-11 | 1981-02-04 | Matsushita Electric Works Ltd | Surface decorating method by granular matter |
-
1978
- 1978-12-25 JP JP16351978A patent/JPS5586566A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5586566A (en) | 1980-06-30 |
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