JPS624347B2 - - Google Patents
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- Publication number
- JPS624347B2 JPS624347B2 JP52145643A JP14564377A JPS624347B2 JP S624347 B2 JPS624347 B2 JP S624347B2 JP 52145643 A JP52145643 A JP 52145643A JP 14564377 A JP14564377 A JP 14564377A JP S624347 B2 JPS624347 B2 JP S624347B2
- Authority
- JP
- Japan
- Prior art keywords
- clay
- weight
- mineral
- polymer
- talc
- 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
Landscapes
- Preparation Of Clay, And Manufacture Of Mixtures Containing Clay Or Cement (AREA)
Description
この発明は、繊維素材粘土と鉱物質粘土との両
方の長所を兼ねて持つ粘土に関するものである。
粘土は古くから造形用の素材として広く利用さ
れ、陶磁器の原材料、学校における造形の教材と
してのみならず、近年は合成樹脂、セルロイド、
ガラス、金属、木材などで成形された造形体の表
面に、薄く延ばして被着せしめ、工芸品や立体地
図を作るなど、その用途はますます拡がりを見せ
ている。
このため粘土においては、(i)造形直後に自重な
どによつて自然変形を起さない保形性(ii)造形体表
面に手あるいはヘラによつて塗り付けられてゆく
際における造形体表面との接着度、(iii)造形体表面
に塗りつけてゆく際における延び、(iv)該塗りつけ
てゆく際における手やヘラに対するベトつきまた
は被着、(v)粘土自体の膚ざわり、(vi)乾燥後におけ
る剥離、(vii)乾燥後における粘土表面のヒビ割れや
膚あいなどが問題となる。
そして上記(i)に云う保形性が十分でないと、造
形後、乾燥して強度が増す以前に、ダレを生じて
変形し、特に造花、人形など厚さや太さを大きく
とれないものにおいてこの現象が著るしい。上記
(ii)に言う接着度が十分でないとき、塗り付けてゆ
く過程において、先に塗りつけた個所が後に塗り
つけられる部分のために引張られていわゆるメク
レ上る形となる。上記(iii)に言う延びが十分でない
とき、造形体表面に押しつけて薄く延ばして被着
することができなくなり、いわば新聞紙などを水
でホグした固まりを造形体表面に押しつけて被着
させるような状態となる。上記(iv)によるベトつき
や被着が強すぎると、造形体表面に被着する代わ
りに手やヘラに被着される量が増し工作がむずか
しくなると共にいわゆる手がよごれる形となる。
上記(v)に言う膚ざわりがよくないとき、表面の平
滑さが失われ、ざらつきが目立つてきていわばボ
ソボソした形となる。上記(vi)に言う乾燥後におけ
る剥離現象が存在すると、折角工作した結果の工
作物表面がマダラになる。上記(vii)に言う乾燥後に
おける粘土表面のヒビ割れが生ずると工作物表面
の美しさが失なわれ、また粘土表面の膚あいが十
分でないと粘土表面に肌あれが目立つて現われた
形となる。
しかし、これらの要求される性質は、例えば保
形性を良好にするため固めの粘土とすれば延びは
当然に悪くなるとか、造形体配合との接着度を良
くしようとすれば、手やヘラの被着もまた大きく
なるなどのように、相互に矛循するものが多く、
良質の粘土を得ることはかなり困難なものであ
る。
従来は、カオリン、ベントナイト等で代表され
る粘土質鉱物を主としたいわゆる粘土が最も広く
用いられている。しかし、これらの鉱物質粘土
は、産地によつて種々の鉱物質を含み、多くは水
分の調整のみによつて使用時の性質を整える結
果、上記の矛循した諸要求を同時に充すことが難
めて困難であり、廉価に入手し得ると云う最大の
特長によつて広く利用されながらも、用途は限ら
れたものとならざるを得ない。
また、木材パルプその他の繊維素材を水中に分
散させ、合成樹脂等の糊料を加えて適当に脱水し
た繊維素材粘土は、造形体への粘着度、造形の際
の延び、乾燥後の強度などが自由に調節し得る上
に、繊維素材自体を染色することによつて着色粘
土とすることが可能であり、鉱物質粘土とは別の
用途に用いられる。しかし、造形直後の保形性、
表面が繊維が表われる結果として雅趣のある表面
を形成させることは出来るが、膚ざわり、膚あい
等が必ずしもよくないこと、乾燥による収縮が激
しく、造形体表面に被着せしめた場合に乾燥後剥
離を生ずる等の欠点を生ずるものである。
この発明は、上記の問題点を考慮して、繊維素
材と粘土鉱物とを配合し、糊材として未ケン化の
アセチル基を含有するポリビニールアルコール水
溶液を用いることにより、上記の問題を解決した
ものである。
本発明による粘土は次のように製造される。即
ち、木材パルプなどの繊維素材を水中で解砕し、
染料または顔料を用いて繊維素材を着色してのち
繊維素材と水分との重量比が100対100または100
対50程度になるまで脱水する。一方、上記未ケン
化のアセチル基を含有するポリビニールアルコー
ルは「デンカHVポリマ」(商標)としてパウダ状
のものが市販されているので、このポリマ粉末に
重量比で約15倍ないし3倍程度の水を加えた上、
必要に応じ適温(約90℃程度)に加熱しつつポリ
マ粉末を溶解せしめて糊材をつくる。該糊材に適
量の防ばい剤を添加する。
さらに鉱物成分として一般には粉末の形態で入
手出来るタルク、クレー(カオリン)、ダイカラ
イト(パーライト)、炭酸カルシウム、ベントナ
イトをそれぞれ目的に応じて粘土の全重量の60%
を越えない分量になるように適宜に選択して混合
する。このうち、タルクは粘土の膚のつやを増
し、クレーはつや出しと同時にのびをよくし、ベ
ントナイトはのびとねばりを増す効果がある。ダ
イカライトと炭酸カルシウムは増量材である。
上述の如く構成された着色素材(水を含む)と
上記糊料(水を含む)及び鉱物成分とを混合して
ねりあわせる。このとき添加物としてポリエチレ
ンオキサイドを全体に対して2重量%程度を加え
て、ベトつきを抑え多少の光沢を与える。
発明者は、種々配合を変えて次の8種の粘土を
実験的に製造し、その特性を比較した。
(A) 上記ポリマ粉末5%と水95%からなる糊料
(ポリマの5%溶液)50%、ポリエチレン オ
キサイド(PEO)16.7%、水83.3%からなる
PEO溶液6%、パルプ8%、クレー17%、タ
ルク9%、ダイカライト10%
(B) 上記ポリマ粉末10%、水90%からなる糊料
(ポリマの10%溶液)50%、PEO溶液6%、パ
ルプ8%、クレー17%、タルク9%、ダイカラ
イト10%
(C) 上記ポリマ粉末15%、水85%からなる糊料
(15%溶液)50%、PEO溶液6%、パルプ8
%、クレー17%、タルク9%、ダイカライト10
%
(D) ポリマ15%溶液54%、PEO溶液6%、パル
プ8%、クレー9%、タルク13%、ダイカライ
ト10%
(E) ポリマ15%溶液49%、PEO溶液6%、パル
プ8%、クレー14%、タルク13%、ダイカライ
ト10%
(F) ポリマ15%溶液68%、PEO溶液2%、パル
プ14%、クレー8%、タルク6%、ベントナイ
ト1.5%
(G) ポリマ18%溶液58.6%、PEO溶液1.4%、パ
ルプ20%、クレー20%
(H) ポリマ10%溶液55%、PEO溶液2%、パル
プ33%、タルク10%
上記の8種類の粘土について、その特性を比較
した結果は次表のようであつた。
This invention relates to a clay that has the advantages of both fibrous clay and mineral clay. Clay has been widely used as a material for modeling since ancient times, and has been used not only as a raw material for ceramics and as a teaching material for modeling in schools, but also in recent years as a material for synthetic resin, celluloid,
Its uses are increasingly expanding, such as by spreading it thinly and applying it to the surface of objects made of glass, metal, wood, etc. to create crafts and three-dimensional maps. For this reason, clay has (i) shape retention that does not cause natural deformation due to its own weight immediately after modeling, and (ii) the ability to maintain the shape of the object surface when it is applied by hand or with a spatula. degree of adhesion, (iii) elongation when applied to the surface of the model, (iv) stickiness or adhesion to the hands or spatula during application, (v) texture of the clay itself, and (vi) dryness. Problems include peeling afterwards and (vii) cracking and roughness of the clay surface after drying. If the shape retention mentioned in (i) above is not sufficient, the shape will sag and deform before it dries and becomes stronger after modeling, especially for things such as artificial flowers and dolls that cannot be made large in thickness or thickness. The phenomenon is remarkable. the above
When the degree of adhesion mentioned in (ii) is not sufficient, during the process of painting, the area that was applied first is pulled by the area that will be applied later, resulting in a so-called "mekure" shape. When the elongation mentioned in (iii) above is not sufficient, it becomes impossible to apply the material by pressing it onto the surface of the object and spreading it thinly. state. If the stickiness or adhesion caused by (iv) above is too strong, the amount of adhesion on the hands and spatula increases instead of on the surface of the modeled object, making the work difficult and causing what is called a dirty hand.
When the texture described in (v) above is not good, the surface loses its smoothness and becomes noticeably rough, giving it a rough shape. If the peeling phenomenon described in (vi) above exists after drying, the surface of the workpiece after painstaking machining will become uneven. If cracks occur on the clay surface after drying as described in (vii) above, the beauty of the surface of the workpiece will be lost, and if the texture of the clay surface is not sufficient, rough skin will appear on the clay surface. Become. However, these required properties are not met, for example, if hardened clay is used to improve shape retention, it will naturally have poor elongation, and if you want to improve the degree of adhesion to the molded object, it will be difficult to use your hands or spatula. There are many things that contradict each other, such as the adhesion of
Obtaining good quality clay is quite difficult. Conventionally, so-called clay, which is mainly composed of clayey minerals such as kaolin and bentonite, has been most widely used. However, these mineral clays contain various mineral substances depending on the region of production, and in many cases, the properties during use are adjusted only by adjusting the moisture content, so it is difficult to simultaneously satisfy the contradictory requirements mentioned above. Although it is widely used due to its greatest feature of being extremely difficult to obtain and being available at a low price, its uses are inevitably limited. In addition, fibrous clay, which is made by dispersing wood pulp or other fibrous materials in water, adding a glue such as a synthetic resin, and dehydrating it appropriately, has properties such as adhesion to objects, elongation during modeling, and strength after drying. In addition to being able to freely adjust the color of the clay, it can be made into colored clay by dyeing the fiber material itself, and is used for purposes other than mineral clay. However, shape retention immediately after modeling,
As a result of the appearance of fibers on the surface, it is possible to form an elegant surface, but the texture and texture are not necessarily good, and the shrinkage due to drying is severe, so when it is applied to the surface of a modeled object, it may be difficult to This causes disadvantages such as peeling. In consideration of the above problems, this invention solves the above problems by blending a fiber material and a clay mineral and using an aqueous polyvinyl alcohol solution containing unsaponified acetyl groups as a glue material. It is something. The clay according to the invention is produced as follows. That is, fiber materials such as wood pulp are crushed in water,
After coloring the fiber material with dyes or pigments, the weight ratio of the fiber material to water is 100:100 or 100.
Dehydrate until it becomes about 50% water. On the other hand, the above-mentioned polyvinyl alcohol containing unsaponified acetyl groups is commercially available in powder form as "Denka HV Polymer" (trademark), so it is about 15 to 3 times the weight ratio of this polymer powder. After adding water,
Glue is made by heating to an appropriate temperature (approximately 90°C) as necessary to dissolve the polymer powder. An appropriate amount of fungicide is added to the paste material. Furthermore, as mineral components, talc, clay (kaolin), dicalite (perlite), calcium carbonate, and bentonite, which are generally available in powder form, can be added to make up 60% of the total weight of the clay depending on the purpose.
Select and mix appropriately so that the amount does not exceed . Of these, talc increases the luster of the clay's skin, clay makes it glossy and spreads well, and bentonite increases its spreadability and stickiness. Dicalite and calcium carbonate are fillers. The colored material (containing water) configured as described above, the above-mentioned paste (containing water) and mineral components are mixed and kneaded together. At this time, polyethylene oxide is added as an additive in an amount of about 2% by weight based on the total weight to suppress stickiness and give some gloss. The inventors experimentally produced the following eight types of clay with various formulations and compared their properties. (A) Thickening material (5% solution of polymer) consisting of 5% of the above polymer powder and 95% water, 50% of polyethylene oxide (PEO), and 83.3% of water.
PEO solution 6%, pulp 8%, clay 17%, talc 9%, dicalite 10% (B) Thickening material (10% polymer solution) consisting of 10% of the above polymer powder and 90% water (10% polymer solution) 50%, PEO solution 6 %, pulp 8%, clay 17%, talc 9%, dicalite 10% (C) Thickening agent (15% solution) consisting of 15% of the above polymer powder and 85% water, 50% PEO solution, 6% pulp, 8% pulp
%, clay 17%, talc 9%, dicalite 10
% (D) Polymer 15% solution 54%, PEO solution 6%, pulp 8%, clay 9%, talc 13%, dicalite 10% (E) Polymer 15% solution 49%, PEO solution 6%, pulp 8% , 14% clay, 13% talc, 10% dicalite (F) 68% 15% polymer solution, 2% PEO solution, 14% pulp, 8% clay, 6% talc, 1.5% bentonite (G) 18% polymer solution 58.6%, PEO solution 1.4%, pulp 20%, clay 20% (H) 10% polymer solution 55%, PEO solution 2%, pulp 33%, talc 10% The properties of the above eight types of clay were compared. The results were as shown in the table below.
【表】
一般にパルプに対するポリマおよび鉱物成分の
重量比が減少するにつれて、粘土自体について繊
維質が目につくようになる。そして造形をしてゆ
くとき、粘土の延びが失なわれ押し延ばすことが
困難となり押圧によつてのみ造形あるいは被着で
きるようになると共に、粘土自体がボソボソした
ものとなる。また乾燥後に粘土表面に凹凸が生じ
たものとなる。また特に造型体がガラスなどの光
沢をもつものに対して、押延して被着しようとす
るときメクレ上る形となつてくる。
また、ポリマの重量比が増大すると、乾燥によ
る収縮が大きくなる。しかし、適量の鉱物成分の
混入によつてこの収縮が減少し、肌あいのあれを
防ぎ、つやが生ずる。
この実施例では何れもHVポリマを用いている
が、PVAもよく知られているように糊材として
利用出来る。HVポリマはPVAに比して高い粘性
を持ち、粘土としてののびや造形体への接着性を
改善する。しかし、これだけでは手やヘラなどに
対するベトつきが生ずるので、PEOを混入する
ことによつて改善する。特性の若干の低下をがま
んすればPEOの代りにコストの廉いPVAで代用
することも出来る。
この効果を上記AないしHの8種類の粘土で具
体的に説明すれば、AからCへとHVポリマの増
加につれ、粘土の性質は著しく改善されるが、収
縮のめは増加する。
BとHを比較すると、Bはパルプが8%にすぎ
ずクレーとダイカライトが計27%混入されている
のに対し、Hはパルプが33%である。その結果H
は肌ざわり、やわらかさは良いが、収縮が大きく
なる。
D、B、Eを比べれば、クレー、タルクが増す
につれ、腰はよくなるが、やわらかさ、ボソつき
が生じ、のびは悪くなる。
FとGとを比べれば、GはPEOが少く、クレ
ー、タルク、ベントナイト成分が多いので手につ
き、パルプの混入量が多いのでベとつきが改善さ
れる。
HとGを比べれば、Hはタルクを10%含むのみ
であるので、HVポリマが少いにもかかわらず、
収縮が大きい。
以上説明したように、この発明によれば、糊
材、繊維成分、鉱物成分の配合により広い成分範
囲でその特性を好みのものに調整出来、肌ざわ
り、のびがよく、腰があり、手等への附着が少な
く、しかも乾燥による収縮の少い極めて勝れた粘
土を調合することが出来るものである。
繊維として、石綿、金属繊維等の無機繊維を用
い、粘土鉱物成分を比較的多めに配合すれば、糊
材によつて造形性を改善し、これを焼いて鉱物成
分を焼結することにより、繊維強化された焼物を
得ることが出来るなど、この発明の粘土は、その
特性を生かして、従来なかつたような用途をひら
くものである。TABLE Generally, as the weight ratio of polymer and mineral components to pulp decreases, the clay itself becomes more visible. Then, when shaping, the clay loses its elasticity and becomes difficult to push, making it possible to shape or adhere only by pressing, and the clay itself becomes crumbly. Moreover, after drying, the clay surface becomes uneven. In addition, especially when the molded object has a glossy finish such as glass, when trying to press and adhere the molded object, the molded object tends to form a sticky shape. Furthermore, as the weight ratio of the polymer increases, shrinkage due to drying increases. However, by incorporating an appropriate amount of mineral ingredients, this shrinkage is reduced, preventing roughness of the skin and creating shine. In this embodiment, HV polymer is used, but PVA can also be used as a glue material, as is well known. HV polymer has higher viscosity than PVA, which improves its spreadability as clay and its adhesion to molded objects. However, this alone causes stickiness to hands, spatulas, etc., which can be improved by incorporating PEO. If a slight decrease in properties is tolerated, PEO can be replaced with cheaper PVA. To specifically explain this effect using the above eight types of clays A to H, as the HV polymer increases from A to C, the properties of the clay are significantly improved, but the degree of shrinkage increases. Comparing B and H, B has only 8% pulp and a total of 27% clay and dicalite mixed in, while H has 33% pulp. As a result H
The texture and softness are good, but the shrinkage is large. Comparing D, B, and E, as the amount of clay and talc increases, the elasticity improves, but softness and roughness occur, and the spreadability worsens. Comparing F and G, G has less PEO and more clay, talc, and bentonite components, so it sticks to your hands, and it has a higher amount of pulp, which improves stickiness. Comparing H and G, H contains only 10% talc, so even though it contains less HV polymer,
Large contraction. As explained above, according to the present invention, the properties can be adjusted to the desired properties over a wide range of ingredients by blending the glue material, fiber components, and mineral components, and the properties can be adjusted to the desired properties, such as texture, spreadability, firmness, and smoothness on the hands. It is possible to prepare an extremely superior clay that has less adhesion to the clay and less shrinkage due to drying. If inorganic fibers such as asbestos or metal fibers are used as fibers and a relatively large amount of clay mineral components are added, the shapeability is improved by the glue, and by baking this and sintering the mineral components, The clay of the present invention takes advantage of its properties, such as the ability to produce fibre-reinforced pottery, and opens up new uses that have not been seen before.
Claims (1)
を配合した粘土において、繊維素材を5ないし30
重量%、糊料である未ケン化のアセチル基を含有
するポリビニルアルコール5ないし20重量%、合
計60重量%以下の鉱物成分粉末1種あるいは2種
以上、2重量%程度の添加物からなり、残部を水
によつて構成したことを特徴とする粘土。 2 上記繊維素材は石綿、金属繊維等の無機繊維
を主成分とする繊維素材よりなることを特徴とす
る特許請求の範囲第1項記載の粘土。 3 上記添加物はポリエチレンオキサイドを含
み、該ポリエチレンオキサイドは上記未ケン化の
アセチル基を含有するポリビニルアルコールに対
して重量比で0.5%ないし20%の範囲で配合され
ることを特徴とする特許請求の範囲第1項または
第2項記載の粘土。 4 鉱物成分はタルク、クレー(カオリン)ダイ
カライト(パーライト)、炭酸カルシウム、ベン
トナイトのうちから1種あるいは2種以上を選択
することを特徴とする特許請求の範囲第1項また
は第2項記載の粘土。[Claims] 1. A clay in which a sizing agent is mixed with crushed fiber material and mineral component powder, in which the fiber material is mixed with 5 to 30% of the fibrous material.
5 to 20% by weight of polyvinyl alcohol containing unsaponified acetyl groups as a thickener, one or more mineral component powders with a total of up to 60% by weight, and about 2% by weight of additives, A clay characterized by the balance being made up of water. 2. The clay according to claim 1, wherein the fibrous material is a fibrous material whose main component is inorganic fibers such as asbestos and metal fibers. 3. A patent claim characterized in that the additive includes polyethylene oxide, and the polyethylene oxide is blended in a weight ratio of 0.5% to 20% with respect to the unsaponified acetyl group-containing polyvinyl alcohol. The clay according to item 1 or 2 of the range. 4. The mineral component according to claim 1 or 2, wherein one or more mineral components are selected from talc, clay (kaolin) dicalite (perlite), calcium carbonate, and bentonite. clay.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14564377A JPS5478718A (en) | 1977-12-06 | 1977-12-06 | Clay |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14564377A JPS5478718A (en) | 1977-12-06 | 1977-12-06 | Clay |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5478718A JPS5478718A (en) | 1979-06-23 |
| JPS624347B2 true JPS624347B2 (en) | 1987-01-29 |
Family
ID=15389747
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14564377A Granted JPS5478718A (en) | 1977-12-06 | 1977-12-06 | Clay |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5478718A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01135947U (en) * | 1988-03-11 | 1989-09-18 |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS56133343A (en) * | 1980-03-24 | 1981-10-19 | Shinwa Service:Kk | Cured material consisting of grain flour essentially |
| JPS56133342A (en) * | 1980-03-24 | 1981-10-19 | Shinwa Service:Kk | Preparation of plastic cured material |
| JPS6076313A (en) * | 1983-10-01 | 1985-04-30 | 木村 栄子 | Muddy clay and usage thereof |
| WO2017064808A1 (en) | 2015-10-16 | 2017-04-20 | 三菱電機株式会社 | Elevator rope and manufacturing method therefor |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4862525A (en) * | 1971-12-04 | 1973-08-31 | ||
| JPS51135946A (en) * | 1975-05-21 | 1976-11-25 | Pajiko:Kk | E ngraving materials |
| JPS5256113A (en) * | 1975-11-04 | 1977-05-09 | Seiji Takagi | Plastic clay compositions |
| JPS5950615B2 (en) * | 1975-12-25 | 1984-12-10 | カブシキガイシヤ バジコ | Seikeizai |
| JPS5338427A (en) * | 1976-09-20 | 1978-04-08 | Tokyo Shibaura Electric Co | Paper clay |
| LU77489A1 (en) * | 1977-06-06 | 1979-01-19 |
-
1977
- 1977-12-06 JP JP14564377A patent/JPS5478718A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01135947U (en) * | 1988-03-11 | 1989-09-18 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5478718A (en) | 1979-06-23 |
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