JPS63277583A - Improved glaze for coating and flame-spraying and glaze application - Google Patents
Improved glaze for coating and flame-spraying and glaze applicationInfo
- Publication number
- JPS63277583A JPS63277583A JP11287587A JP11287587A JPS63277583A JP S63277583 A JPS63277583 A JP S63277583A JP 11287587 A JP11287587 A JP 11287587A JP 11287587 A JP11287587 A JP 11287587A JP S63277583 A JPS63277583 A JP S63277583A
- Authority
- JP
- Japan
- Prior art keywords
- glaze
- heat
- inorganic substance
- glass
- flame
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000011248 coating agent Substances 0.000 title claims abstract description 8
- 238000000576 coating method Methods 0.000 title claims abstract description 8
- 238000010285 flame spraying Methods 0.000 title description 3
- 239000000126 substance Substances 0.000 claims abstract description 13
- 239000011521 glass Substances 0.000 claims abstract description 12
- 235000019353 potassium silicate Nutrition 0.000 claims abstract description 10
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000000853 adhesive Substances 0.000 claims description 11
- 230000001070 adhesive effect Effects 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 8
- 238000005507 spraying Methods 0.000 claims description 7
- 238000007751 thermal spraying Methods 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 3
- 150000007529 inorganic bases Chemical class 0.000 claims 2
- 239000000758 substrate Substances 0.000 abstract description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 7
- 239000000203 mixture Substances 0.000 abstract description 6
- 238000002844 melting Methods 0.000 abstract description 4
- 230000008018 melting Effects 0.000 abstract description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 3
- 239000003513 alkali Substances 0.000 abstract description 3
- 239000011230 binding agent Substances 0.000 abstract description 3
- 239000004927 clay Substances 0.000 abstract description 2
- 239000003792 electrolyte Substances 0.000 abstract description 2
- 239000000049 pigment Substances 0.000 abstract description 2
- 229910052681 coesite Inorganic materials 0.000 abstract 1
- 229910052906 cristobalite Inorganic materials 0.000 abstract 1
- 239000010419 fine particle Substances 0.000 abstract 1
- 239000002245 particle Substances 0.000 abstract 1
- 239000000377 silicon dioxide Substances 0.000 abstract 1
- 235000012239 silicon dioxide Nutrition 0.000 abstract 1
- 229910052682 stishovite Inorganic materials 0.000 abstract 1
- 229910052905 tridymite Inorganic materials 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 18
- 239000002585 base Substances 0.000 description 12
- 239000007921 spray Substances 0.000 description 11
- 239000007789 gas Substances 0.000 description 4
- 229910010272 inorganic material Inorganic materials 0.000 description 4
- 239000011147 inorganic material Substances 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical class OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000010454 slate Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 241000951471 Citrus junos Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000004111 Potassium silicate Substances 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 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
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- -1 boric acid esters Chemical class 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000004566 building material Substances 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
- 239000000919 ceramic Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- PAZHGORSDKKUPI-UHFFFAOYSA-N lithium metasilicate Chemical compound [Li+].[Li+].[O-][Si]([O-])=O PAZHGORSDKKUPI-UHFFFAOYSA-N 0.000 description 1
- 229910052912 lithium silicate Inorganic materials 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- GVALZJMUIHGIMD-UHFFFAOYSA-H magnesium phosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GVALZJMUIHGIMD-UHFFFAOYSA-H 0.000 description 1
- 239000004137 magnesium phosphate Substances 0.000 description 1
- 229960002261 magnesium phosphate Drugs 0.000 description 1
- 229910000157 magnesium phosphate Inorganic materials 0.000 description 1
- 235000010994 magnesium phosphates Nutrition 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 238000007750 plasma spraying Methods 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- 229910052913 potassium silicate Inorganic materials 0.000 description 1
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 description 1
- 239000005368 silicate glass Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 235000011008 sodium phosphates Nutrition 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- WUUHFRRPHJEEKV-UHFFFAOYSA-N tripotassium borate Chemical compound [K+].[K+].[K+].[O-]B([O-])[O-] WUUHFRRPHJEEKV-UHFFFAOYSA-N 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
Landscapes
- Glass Compositions (AREA)
Abstract
Description
【発明の詳細な説明】
E産業上の利用分野]
本発明は改良された塗布・溶射用ガラ・ス質釉薬および
その施釉法に関する。詳しくは、釉薬に耐熱付着性無機
系物質を添加混合してなり、基材上へ塗布した該釉薬の
熔融時の付着力(融着力)を増大させた上記の釉薬およ
びその施釉法に関する。DETAILED DESCRIPTION OF THE INVENTION E-INDUSTRIAL APPLICATION FIELD The present invention relates to an improved glass glaze for coating and thermal spraying and a method for applying the same. Specifically, the present invention relates to the above-mentioned glaze, which is made by adding and mixing a heat-resistant adhesion inorganic substance to the glaze, and which increases the adhesion force (fusion force) when the glaze is melted and coated onto a base material, and a method for applying the glaze.
[従来の技術およびその問題点コ
建材用基材、特にコンクリート板、スレート板等の相対
的に低耐熱性の基材上に施釉して釉層を形成する場合、
該基材上に釉薬を塗布した後、プラズマ又はガス式溶射
装置、或いはその他の表面加熱装置を移動させるか該基
材を移動させて、該装置からの溶射炎又は熱により該基
材上の釉薬を溶かして、ガラス質層を形成する方法が知
られている。[Prior art and its problems] When forming a glaze layer by applying glaze to a base material for building materials, especially a base material with relatively low heat resistance such as a concrete board or a slate board,
After the glaze is applied to the substrate, a plasma or gas spraying device or other surface heating device is moved or the substrate is moved so that the spray flame or heat from the device coats the substrate. A method is known in which a glaze is melted to form a glassy layer.
該釉薬は従来、釉薬原料となるガラスフリツ)、を充分
綿層し、これに有機質バインダーを適量添加して適度の
粘性を有する泥漿として安定化させることにより製造さ
れ、泥漿の形体でエアースプレー等により基材上に塗布
される。塗布により形成された釉層を上記のような溶射
加熱装置等により溶かしてガラス層として基材上に融着
させる。The glaze is conventionally manufactured by making a sufficient cotton layer of glass fritz, which is the raw material for the glaze, and adding an appropriate amount of an organic binder to this to stabilize it as a slurry with an appropriate viscosity. applied onto the substrate. The glaze layer formed by coating is melted using a thermal spray heating device such as the one described above, and is fused onto the base material as a glass layer.
しかしながら、その際、溶射装置等から発生する溶射炎
等の勢いによって釉層が溶けてガラス層が形成される前
に、該塗布層が剥離する危険性が大きかった。また、基
材の中には釉薬との濡れ性(なじみ)が悪く、溶射炎等
による釉薬の熔融時に釉層が剥離することがある。However, in this case, there was a large risk that the coating layer would peel off before the glaze layer was melted by the force of the spray flame generated from a thermal spraying device or the like and the glass layer was formed. Furthermore, some base materials have poor wettability (compatibility) with the glaze, and the glaze layer may peel off when the glaze is melted by a thermal spray flame or the like.
」二記のような現象は、釉薬を塗布した基材全体をトン
ネルキルンで焼成(約30時間前後)または高速度焼成
炉で焼成(約1時間以」二)する場合には、発生しない
現象である。これに対し、プラズマ炎またはガス炎の照
射による加熱溶射等では釉薬は実質的に瞬時に熔融する
ので、このような現象が生起するものと考えられる。The phenomenon described in item 2 does not occur if the entire glazed base material is fired in a tunnel kiln (approximately 30 hours) or in a high-speed firing furnace (approximately 1 hour or more). It is. On the other hand, in thermal spraying using plasma flame or gas flame irradiation, the glaze melts substantially instantaneously, so this phenomenon is thought to occur.
従って本発明の目的は、従来の釉薬の溶射熔融時におけ
る基材への低い付着力を改良し、両番の濡れ性を改良し
た釉薬およびその使用法を提供することにある。Accordingly, an object of the present invention is to provide a glaze that improves the low adhesion of conventional glazes to substrates during thermal spray melting and improves both wettability, and a method for using the same.
[問題点を解決するための手段]
本発明の改良された釉薬は、釉薬中のガラスフリット1
00重量部に対して約1〜約40重量部の水溶性または
ゾル形成性の耐熱付着性無機系物質が添加混合されてい
ることを特徴とする。[Means for solving the problems] The improved glaze of the present invention has glass frit 1 in the glaze.
It is characterized in that about 1 to about 40 parts by weight of a water-soluble or sol-forming heat-resistant adhesion inorganic material is added and mixed to 00 parts by weight.
上記の釉薬は、釉薬原料のガラスフリットおよび必要に
応じて粘土、電解質、水、顔料等をボールミル等により
充分綿層し、これに必要に応じて適量の有機質バインダ
ー(例えばメチルセルロース、ポリビニルアルコール、
澱粉等)と共に、上記の耐熱付着性無機系物質を1記範
囲の量で加え、十分に混合することにより製造できる。The above glaze is made by thoroughly layering glass frit as a glaze raw material and, if necessary, clay, electrolyte, water, pigment, etc. using a ball mill or the like, and adding an appropriate amount of organic binder (for example, methyl cellulose, polyvinyl alcohol,
It can be produced by adding the above-mentioned heat-resistant adhesive inorganic substance in an amount within the range 1 above with starch, etc., and mixing thoroughly.
上記の耐熱付着性無機系物質としては、水ガラス;およ
びリン酸系化合物(例えばリン酸アルミニウム、リン酸
ナトリウム、リン酸カリウム、リン酸マグネシウム、リ
ン酸およびリン酸エステル)、ホウ酸系化合物(例えば
ホウ酸ナトリウム、ホウ酸カリウム、ホウ酸およびホウ
酸エステル)、ケイ酸エステル、コロイダルシリカ、ア
ルミナゾル等の濃厚水溶液または水性ゾル、が例示され
る。Examples of the above-mentioned heat-resistant adhesive inorganic substances include water glass; phosphoric acid compounds (e.g. aluminum phosphate, sodium phosphate, potassium phosphate, magnesium phosphate, phosphoric acid and phosphoric esters), boric acid compounds ( For example, concentrated aqueous solutions or aqueous sols such as sodium borate, potassium borate, boric acid and boric acid esters), silicate esters, colloidal silica, and alumina sol are exemplified.
代表的には水ガラスが使用される。Water glass is typically used.
上記の水ガラスとは、アルカリ−ケイ酸塩系ガラスの濃
厚水溶液(通常約30重量%以上)を意味する。ここで
該アルカリとは一般にNatOlLizOおよび/また
はKtoであり、5ift/アルカリのモル比は通常2
.1〜3.5である。例えば、ケイ酸リチウム、ケイ酸
ナトリウム、およびケイ酸カリウムの濃厚水溶液が例示
され、通常市販の水ガラス[組成(重量比)、5rOt
:30%、NatO: 10%、水二60%コが使用さ
れる。The above-mentioned water glass means a concentrated aqueous solution (usually about 30% by weight or more) of an alkali-silicate glass. Here, the alkali is generally NatOlLizO and/or Kto, and the molar ratio of 5ift/alkali is usually 2.
.. 1 to 3.5. For example, concentrated aqueous solutions of lithium silicate, sodium silicate, and potassium silicate are exemplified, and commercially available water glass [composition (weight ratio), 5rOt]
: 30%, NatO: 10%, and Water: 60%.
該耐熱付着性無機系物質の添加量は、釉薬中のガラスフ
リット100重量部に対して一般に約1〜約40重量部
、好ましくは約3〜約30重量部、更に好ましくは約5
〜約20重看部程度である。The amount of the heat-resistant adhesive inorganic substance added is generally about 1 to about 40 parts by weight, preferably about 3 to about 30 parts by weight, and more preferably about 5 parts by weight, based on 100 parts by weight of the glass frit in the glaze.
~ Approximately 20 degrees of weight.
本発明の釉薬を用いて基材上に釉層を形成するには、ま
ずエアースプレー、幕かけ法等により該釉薬を基材表面
に塗布し、施釉面を乾燥させた後、プラズマ溶射装置、
火炎溶射装置、遠赤外線炉等により施釉表面を加熱して
釉層の少なくとも表面を熔融させて、ガラス質柚層を得
る。溶射装置を用いる場合は、溶射ガンを施釉面に垂直
に向けて熱が効率よく利用できるようにするのが好まし
い。To form a glaze layer on a substrate using the glaze of the present invention, first apply the glaze to the surface of the substrate by air spraying, curtaining method, etc., dry the glazed surface, and then use a plasma spraying device.
The glazed surface is heated using a flame spraying device, a far infrared furnace, etc. to melt at least the surface of the glaze layer, thereby obtaining a vitreous yuzu layer. If a thermal spray device is used, it is preferable to orient the thermal spray gun perpendicularly to the glazed surface to ensure efficient heat utilization.
該釉薬の塗布前に、基材表面に前記の耐熱付着性無機系
物質を塗布すると、釉層の耐剥離性が一層向上する。こ
の場合の耐熱付着性無機系物質の塗布量は通常的0.5
〜約5g/100cm’である。If the heat-resistant adhesive inorganic substance described above is applied to the surface of the base material before applying the glaze, the peeling resistance of the glaze layer is further improved. In this case, the amount of heat-resistant adhesive inorganic material applied is usually 0.5
~about 5 g/100 cm'.
該無機系物質の塗布は、はけ塗り又はスプレー塗布のい
ずれでもよい。The inorganic material may be applied by brushing or spraying.
本発明の釉薬は、従来の釉薬と同程度の割合で基材上に
塗布され通常約1〜約100g/100cm″、代表的
には約2〜約30g/100cm’の割合で塗布される
。得られる釉層の厚さは通常的0.Immから数mmで
ある。The glazes of the present invention are applied to the substrate at a rate comparable to conventional glazes, usually from about 1 to about 100 g/100 cm'', typically from about 2 to about 30 g/100 cm''. The thickness of the resulting glaze layer is typically from 0.1 mm to several mm.
本発明の釉薬は、コンクリート板、スレート板等の施油
に有用であるが、セラミックタイル板、金属板およびそ
の他の比較的耐熱性のある無機質店打上にも有利に用い
ることができる。The glaze of the present invention is useful for lubricating concrete boards, slate boards, etc., but it can also be advantageously used for ceramic tile boards, metal boards, and other relatively heat-resistant inorganic materials.
[実施例] 本発明を以下の実施例により、更に具体的に説明する。[Example] The present invention will be explained in more detail with reference to the following examples.
実施例1ニ
ガラスフリット(重量組成は下記表1の通り)2000
gおよび水800gを磁器製ボールミルに入れ、4昼夜
回転した。得られたスラリーに、カルボキシメチルセル
ロース3%溶液を200〜300g、および市販の水ガ
ラス(重量組成;5ift:30%、Na*O:10%
、水:60%)300gを加え、30分間撹狐毘合した
。混合後、100メツシユの篩を通して、スプレーする
際に目詰まりが生じないように大粒の固まりを除去した
。このようにして調製された釉薬をコンクリート基材(
寸法300x300X80mm)上に、エアースプレー
装置にて50g塗布した。その後気中にて1時間放置乾
燥した。次いでプラズマテクニック社製PT−A200
0型プラズマ溶射ガンを用い、下記の条件で釉薬塗膜だ
けを熔融したプラズマ炎走査速度:50〜15mm/秒
走査幅 :2mm
基材−プラズマガン間距M:9〜12cmプラズマ発生
条件=400〜600A。Example 1 Nigarasu frit (weight composition is as shown in Table 1 below) 2000
g and 800 g of water were placed in a porcelain ball mill and rotated for 4 days and nights. 200 to 300 g of a 3% carboxymethylcellulose solution and commercially available water glass (weight composition; 5ift: 30%, Na*O: 10%) were added to the obtained slurry.
, water: 60%) was added, and the mixture was stirred for 30 minutes. After mixing, the mixture was passed through a 100-mesh sieve to remove large clumps to prevent clogging during spraying. The glaze prepared in this way is applied to the concrete base (
50 g of the sample was applied onto a surface (size: 300 x 300 x 80 mm) using an air spray device. Thereafter, it was left to dry in the air for 1 hour. Next, PT-A200 manufactured by Plasma Technique Co., Ltd.
Using a type 0 plasma spray gun, only the glaze coating was melted under the following conditions. Plasma flame scanning speed: 50-15 mm/sec Scanning width: 2 mm Distance between substrate and plasma gun M: 9-12 cm Plasma generation conditions = 400- 600A.
65〜75v。65-75v.
Ar流量〜60Q/分。Ar flow rate ~60Q/min.
H2流量lO〜1512/分。H2 flow rate lO~1512/min.
表 1
LigO0〜5% Z n OO〜10%N a tO
O〜10%B tO31〜20%K tOO〜lO%A
lt030〜15%MgO0〜5% S i Ot 2
0〜50%Ca0O〜5% Z r Ot 5〜10%
このようにして、釉層の光沢面が得られた。従来の釉薬
を用いた場合には溶射時に釉層の剥離がしばしば生じた
のに対して、本実施例の釉層は全く剥離が生じなかった
。また該釉薬は従来の釉薬よりも融点が多少低下してい
るため、低出力で良好な光沢面が得られた。Table 1 LigO0-5% Z n OO-10% Na tO
O~10%B tO31~20%K tOO~lO%A
lt030~15% MgO0~5% S i Ot 2
0-50% Ca0O-5% Z r Ot 5-10%
In this way, a glossy surface of the glaze layer was obtained. When a conventional glaze was used, the glaze layer often peeled off during thermal spraying, whereas the glaze layer of this example did not peel off at all. Furthermore, since the glaze has a somewhat lower melting point than conventional glazes, a good glossy surface could be obtained with low output.
実施例2:
タイル素焼素地(loOXloOmm角)上に、実施例
1と同様にして調製した釉薬をエアースプレーにて約5
g塗布した。その後気中にて約1時間放置して、施釉面
を乾燥させた。次いでメテコ社製5Fガン(ガス式溶射
装置)の火炎を用いて、下記の条件で釉薬塗膜だけを熔
融した:火炎走査速度=5〜20mm/秒
走査幅 :5〜20mm
基材−溶射ガン間距離二12〜20cmガス流量 :
酸素 35a/分、
アセチレン 35Q/分。Example 2: Approximately 50% of the glaze prepared in the same manner as in Example 1 was applied onto the unglazed tile base (loOXloOmm square) by air spraying.
g was applied. Thereafter, it was left in the air for about 1 hour to dry the glazed surface. Then, using the flame of a Metco 5F gun (gas spraying device), only the glaze coating was melted under the following conditions: Flame scanning speed = 5 to 20 mm/sec Scanning width: 5 to 20 mm Base material - Thermal spray gun Distance: 212~20cm Gas flow rate:
Oxygen 35a/min, acetylene 35Q/min.
このようにして、タイル素地上に施釉層の光沢面が得ら
れた。該施釉層は火炎溶射時に全く剥離を生じなかった
。また本例で使用した釉薬は従来の釉薬よりも融点が多
少低下しているため、走査速度を大きくしても良好な光
沢面が得られた。In this way, a glossy surface of the glazed layer on the tile base was obtained. The glazed layer did not peel off at all during flame spraying. Furthermore, since the glaze used in this example had a somewhat lower melting point than conventional glazes, a good glossy surface was obtained even when the scanning speed was increased.
実施例3:
タイル素焼素地(100x100mm角)上に、はけで
市販の水ガラス(Sift:30%。Example 3: Brush commercially available water glass (Sift: 30%) onto a tile unglazed base (100 x 100 mm square).
Na、O:IQ%、水=60%)を約1g塗布し、その
上、に実施例1で調製した水ガラス添加釉薬を約5gエ
アースプレーで塗布した。その後気中で2時間放置して
施油面を乾燥させた。次いで実施例2と同じ装置を用い
同一条件にて釉薬塗膜を熔融して、光沢面を得た。溶射
時に施油面の剥離は生ぜず、面状態は良好であった。ま
た走査速度を大きくしても良好な光沢面が得られた。About 1 g of Na, O: IQ%, water = 60%) was applied, and on top of that, about 5 g of the water glass-added glaze prepared in Example 1 was applied by air spray. Thereafter, the oiled surface was dried by leaving it in the air for 2 hours. The glaze coating was then melted using the same equipment as in Example 2 under the same conditions to obtain a glossy surface. No peeling occurred on the oiled surface during thermal spraying, and the surface condition was good. Further, even when the scanning speed was increased, a good glossy surface was obtained.
[作用および効果][Action and effect]
Claims (6)
て1〜40重量部の耐熱付着性無機系物質が添加・混合
されていることを特徴とする、塗布・加熱溶射用の釉薬
。(1) A glaze for coating and thermal spraying, characterized in that 1 to 40 parts by weight of a heat-resistant adhesive inorganic substance is added and mixed with 100 parts by weight of a glass frit component in the glaze.
特許請求の範囲第1項の釉薬。(2) the heat-resistant adhesive inorganic substance is water glass;
The glaze according to claim 1.
フリット成分100重量部に対して3〜30重量部であ
る、特許請求の範囲第1または第2項の釉薬。(3) The glaze according to claim 1 or 2, wherein the amount of the heat-resistant adhesive inorganic substance added is 3 to 30 parts by weight per 100 parts by weight of the glass frit component.
重量部に対して1〜40重量部の耐熱付着性無機系物質
が添加・混合された釉薬を塗布し、次いで施釉表面を加
熱溶射して釉層を熔融させてガラス質釉層を形成させる
ことを特徴とする、施釉法。(4) Glass frit component 100% on the surface of the inorganic base material
Applying a glaze to which 1 to 40 parts by weight of a heat-resistant adhesive inorganic substance is added and mixed, and then heating and spraying the glazed surface to melt the glaze layer and form a vitreous glaze layer. A glazing method characterized by
付着性無機系物質を塗布する、特許請求の範囲第4項の
方法。(5) The method according to claim 4, wherein a heat-resistant adhesive inorganic substance is applied onto the surface of the inorganic base material before applying the glaze.
特許請求の範囲第4または第5項の方法。(6) the heat-resistant adhesive inorganic substance is water glass;
The method according to claim 4 or 5.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11287587A JPS63277583A (en) | 1987-05-07 | 1987-05-07 | Improved glaze for coating and flame-spraying and glaze application |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11287587A JPS63277583A (en) | 1987-05-07 | 1987-05-07 | Improved glaze for coating and flame-spraying and glaze application |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63277583A true JPS63277583A (en) | 1988-11-15 |
Family
ID=14597716
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11287587A Pending JPS63277583A (en) | 1987-05-07 | 1987-05-07 | Improved glaze for coating and flame-spraying and glaze application |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63277583A (en) |
-
1987
- 1987-05-07 JP JP11287587A patent/JPS63277583A/en active Pending
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