JPS5849769A - Method for reusing urea used in precision casting - Google Patents

Method for reusing urea used in precision casting

Info

Publication number
JPS5849769A
JPS5849769A JP14017781A JP14017781A JPS5849769A JP S5849769 A JPS5849769 A JP S5849769A JP 14017781 A JP14017781 A JP 14017781A JP 14017781 A JP14017781 A JP 14017781A JP S5849769 A JPS5849769 A JP S5849769A
Authority
JP
Japan
Prior art keywords
aldehyde
urea
resorcinol
area
resin
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
Application number
JP14017781A
Other languages
Japanese (ja)
Inventor
Seiji Kawaguchi
河口 清司
Takahiko Murase
村瀬 孝彦
Seinosuke Horiki
堀木 清之助
Kuninori Ito
邦矩 伊藤
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nagoya Yukagaku Kogyo KK
Toyota Motor Corp
Original Assignee
Nagoya Yukagaku Kogyo KK
Toyota Motor Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nagoya Yukagaku Kogyo KK, Toyota Motor Corp filed Critical Nagoya Yukagaku Kogyo KK
Priority to JP14017781A priority Critical patent/JPS5849769A/en
Publication of JPS5849769A publication Critical patent/JPS5849769A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain an adhesive having long potlife and excellent water resistance, boiling resistance, and weather resistance, by adding an aldehyde, etc. to urea flowed out during the precision casing process, and adding a resorcinol resin to the resultant urea precondensate. CONSTITUTION:Urea flowed out during the precision casting process using urea as the lost material is (preferably after leaving to stand under hot condition and removing the bleeded higher fatty acid and wax from the urea) mixed with an aldehyde such as formaldehyde or an aldehyde donor such as paraformaldehyde, and made to react under heating in the presence of an alkali catalyst to obtain a urea precondensate, which is converted to and utilized as an adhesive by adding a resorcinol resin[a condensation product of resorcinol compound such as resorcinol, alkylresorcinol, etc. and an aldehyde (donor)]. USE:Bonding of wood, textile, plastics, rubber, etc.

Description

【発明の詳細な説明】 本発明社精密綺造法に用−たエリアの再利用方法に関す
るものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for reusing an area used in the precision cleaning method.

精密鋳造法とけ水溶性物質、熱溶融性物質等を消失性物
質とし、該消失性物質によってまず鋳造せんとする゛物
品と相似の模型を造り、該模型の周表面に耐火物泥漿を
塗布して鋳型を造り、該鋳型内部の模型を水、蒸気、熱
等で溶出せしめることによって鋳型を製造するものであ
る。そして消失性物質としてエリアを用いる方法は特に
SUP法と言われて―る。上記のようにエリアを消失性
物質として用いるSUP法におψてはエリア溶出物が多
量に生ずるが、従来社これを産業廃棄物として焼却処分
されて≠た。しかしエリア溶出物には多量のエリアが含
有されてφるからこれを単に焼却廃棄することは望まし
―ものではない。そこでエリア溶出物のエリアをホルム
アルデヒド等と縮合させてエリア樹脂とし、これを接着
剤として用いる方法が提案された。しかしBUP法にお
けるエリア溶出物は単にエリアのみでなくそれ以外に多
価アルコール等の第8成分をかなりの量含むものであり
、したがって市販のエリア樹脂系接着剤に比して耐水性
、耐煮沸性、耐候性が著るしく劣り実用性のある接着剤
を得ること社出来なかった。
In precision casting, a water-soluble substance, a heat-fusible substance, etc. is used as a fugitive substance, and a model similar to the article to be cast is first made using the fugitive substance, and a refractory slurry is applied to the peripheral surface of the model. The mold is manufactured by making a mold, and then dissolving the model inside the mold with water, steam, heat, etc. The method using area as a vanishing substance is particularly called the SUP method. As mentioned above, in the SUP method using area as a fugitive substance, a large amount of area eluate is generated, but in the past, this was incinerated as industrial waste. However, since the area eluate contains a large amount of area, it is not desirable to simply dispose of it by incineration. Therefore, a method has been proposed in which the area eluate is condensed with formaldehyde or the like to form an area resin, and this is used as an adhesive. However, the area eluate in the BUP method contains not only area but also a considerable amount of the eighth component such as polyhydric alcohol, and therefore has better water resistance and boiling resistance than commercially available area resin adhesives. It was not possible to obtain a practical adhesive due to the extremely poor properties and weather resistance.

氷見切れ上記従来の欠点を改良して精密鋳造法において
生ずるエリア溶出物を用−て実用性に富む接着剤を製造
し、もってエリア溶出物の高度利用を図ることを目的と
し、エリア溶出物とアルデヒトとの初期縮合物にレゾル
シノール系樹脂を添加することを骨子とするものである
With the aim of improving the above-mentioned conventional drawbacks and producing highly practical adhesives using the area eluates generated in the precision casting process, and thereby achieving advanced utilization of the area eluates, The gist of this method is to add a resorcinol resin to the initial condensate with aldehyde.

レゾルシノール系樹脂をエリア溶出物とアルデヒドとの
初期縮合物に添加することによって、実用性の極めて高
−耐水性、耐煮沸性、耐候性の大きな接着剤が得られる
。即ちレゾルシノール系樹脂はアルデヒドによって硬化
して耐水性、耐煮沸性、耐候性の大きな接着を提供する
が、一方レゾルシノール系樹脂は硬化速度が常温でも早
いからアルデヒドを添加してからの可使時間が短かく実
用性に開−があったがエリア溶出物の存在により可使時
間が延長せられ、かくしてレゾルシノール系樹脂とエリ
ア溶出物とアルデヒドとの初期縮合物とは混合されて相
互の欠点を相補ない実用性の高−接着剤を提供するので
あろう 本発明を以下に詳細に説明する。
By adding resorcinol resin to the initial condensate of area eluate and aldehyde, a practical adhesive with extremely high water resistance, boiling resistance, and weather resistance can be obtained. In other words, resorcinol-based resins are cured by aldehydes and provide adhesives with great water resistance, boiling resistance, and weather resistance.On the other hand, resorcinol-based resins cure quickly even at room temperature, so the pot life after adding aldehydes is shortened. Although it was short-lived and had limited practicality, the presence of the area eluate extended the pot life, and thus the resorcinol resin, the area eluate, and the initial condensate of aldehyde were mixed and compensated for each other's shortcomings. The present invention, which will provide a highly practical adhesive that does not exist, will now be described in detail.

本発明に用いられるエリア溶出物とけ常法によってエリ
アにより鋳造せんとする物品と相似の模型を造り、該模
型の周表面に耐火物泥漿を塗布して鋳型を造り、該鋳型
内部からエリアを水、蒸気、熱等によって溶出せしめた
ものを言う。通常該ユリア溶出物にはエリアの他に多価
アルコール、高級脂肪酸、ワックス等が含まれ、該エリ
ア溶出物を加温放置すると高級脂肪酸、ワックス等が析
出するからこれらを除去した後使用する。高級脂肪酸や
ワックスを除去した後のエリア溶出物としては例えば次
のような組成のものがある。
A model similar to the article to be cast is made by the area using a conventional method for dissolving the area eluates used in the present invention, a mold is made by applying refractory slurry to the peripheral surface of the model, and the area is water-filled from inside the mold. , refers to substances eluted by steam, heat, etc. Generally, the urea eluate contains polyhydric alcohols, higher fatty acids, waxes, etc. in addition to urea, and since higher fatty acids, waxes, etc. will precipitate if the urea eluate is left to warm, it is used after removing these. Area eluates after removal of higher fatty acids and waxes have the following compositions, for example.

エリア          75 重量%多価アルコー
ル       t3 高級脂肪@          q、 gワックス  
        21 その他           2j 水                  2I上記エリ
ア溶出物にはアルデヒドもしくけアルデヒド供与体が添
加され・、アルカリ触媒の存在下で常法により加熱反応
せしめて初期縮合物となす。
Area 75 Weight% polyhydric alcohol t3 Higher fat @ q, g wax
21 Others 2j Water 2I An aldehyde or an aldehyde donor is added to the above-mentioned area eluate and reacted by heating in the presence of an alkali catalyst by a conventional method to form an initial condensate.

上記アルデヒドとはホルムアルデヒド、アセトアルデヒ
ド、n−ブチルアルデヒド アクロレイン、7ラン等の
アルデヒド基を有する化合物のすべてを含み、上記アル
デヒド供給体と#iパラホルムアルデヒド、ヘキサメチ
レンテトラミン、α−ポリオキシメチレン等の分解して
アルデヒドを生成するすべての化合物を言う◇ 上記初期縮合物を製造する際、所望なれば千オ尿素、エ
チレン尿素、メラミン、グ、アニジン、グアナミン、ジ
シアン、ジアミド、フェノール、アルキルフェノール、
フルフリルアルコール等のエリアと共縮合可能な化合物
、ある−はエリアを変。
The above aldehyde includes all compounds having an aldehyde group such as formaldehyde, acetaldehyde, n-butyraldehyde, acrolein, and 7ran, and decomposition of the above aldehyde supplier and #i paraformaldehyde, hexamethylenetetramine, α-polyoxymethylene, etc. ◇ When producing the above initial condensate, if desired, 1,000 urea, ethylene urea, melamine, guanine, anidine, guanamine, dicyan, diamide, phenol, alkylphenol,
Compounds that can be co-condensed with areas such as furfuryl alcohol, certain - changes the area.

性させる化合物を添加してもよい。A compound may be added that causes the reaction to occur.

上記初期縮合物に添加されるレゾルシノール系樹脂とは
レゾルシノール系化合物とアルデヒドもしくはアルデヒ
ド供与体との縮合生成物を言う。
The resorcinol resin added to the above-mentioned initial condensate refers to a condensation product of a resorcinol compound and an aldehyde or an aldehyde donor.

ここにレゾルシノール系化合物とは、レゾルシノール又
はレゾルシノールの1個又#i2個以上のアルキル置換
体をいう。アルキル基Ifi■シ〈はm素数がlないし
ダ個であり、かかるアルキル基としてはメチル基、エチ
ル基、n−プロピル基、1za−プロピル基、n−ブチ
ル基、1zo−ブチル基、tart−ブチル基等がある
。これらC数がダ以下のアルキル基を置換体として有す
るレゾルシノール社、オイルシェールの乾漆時に副生ず
るから安価に入手できる。しかし、炭素数5以上のアル
キル基を置換基に有するレゾルシノールでも本発明の目
的は容易に達成することができるから、アルキル基の炭
素数社本発明の限定にはならな−。レゾルシノール系化
合物ll1一種以上相互に混合されたものであってもよ
い。特にオイルシェールから乾溜時Km生するレゾルシ
ノール系化合物は、S−メチルレゾルシノール、S−エ
チルレゾルシノール、ダ、2j−ジメチルレゾルシノー
ル、コ、!−ジメチルレゾルシ、ノール等の!置換アル
キルレゾルシノールを主成分とす、るアルキルレゾルシ
ノール混合物であり、アルデヒドとの反応性が極めて高
≠。又所望ならば上記オイルシェール・し、ゾルシノー
ル混合物社、分別蒸溜して特定の溜升のみを用いてもよ
ψ。更にアルデヒド4L<はアルデヒド供与体とは上記
初期縮合物に用−られるアルデヒドもしくはアルデヒド
供与体と同様な化合物が用−られる。
The resorcinol compound herein refers to resorcinol or one or #i2 or more alkyl substituted products of resorcinol. The alkyl group Ifi is a prime number of l to da, and such alkyl groups include methyl group, ethyl group, n-propyl group, 1za-propyl group, n-butyl group, 1zo-butyl group, tart- There are butyl groups, etc. Resorcinol Co., Ltd., which has an alkyl group with a C number of 0 or less as a substituent, is produced as a by-product during dry lacquering of oil shale and can be obtained at low cost. However, since the object of the present invention can be easily achieved even with resorcinol having an alkyl group having 5 or more carbon atoms as a substituent, the present invention is not limited to the number of carbon atoms in the alkyl group. One or more resorcinol compounds may be mixed with each other. In particular, resorcinol compounds that are produced from oil shale during dry distillation include S-methylresorcinol, S-ethylresorcinol, da, 2j-dimethylresorcinol, co,! - Dimethyl resorci, norl, etc.! It is an alkylresorcinol mixture whose main component is substituted alkylresorcinol, and it has extremely high reactivity with aldehydes. If desired, the oil shale may be fractionally distilled and only a specific distillate may be used. Furthermore, for aldehyde 4L, the aldehyde donor used is the aldehyde used in the above-mentioned initial condensate or a compound similar to the aldehyde donor.

上記レゾルシノール系化合物とアルデヒドもしくはアル
デヒド供与体とけ常法により縮合されるカ、所望なれば
フェノール、アルキルフェノール、カテコール、アルキ
ルカテコール、ハイドロキノン、アルキルハイドロキノ
ン、ピロガロール、フロログリシン、尿素メラミン、千
オ尿素、ベンゾグアナミン、トルエン、キシレン、クマ
リノ、シクロヘキサノン、カシューオイル、タンニン類
、七ランク、ダンマー、ロジンまたけ胃ジン誘導体、石
油11脂、メタノール、エタノール、イソプロパツール
、N−ブタノール、エチレングリフール、グリセリン等
のポリグリコール、フルフリルアルコール等を添加し、
共縮合又は変性してもさしつかえない。又縮合調整剤と
してアセトン、と−力プルラクタム等のカルボニル基含
有化合物を添加してもよい。
The above-mentioned resorcinol compound and an aldehyde or an aldehyde donor are condensed by a conventional method, if desired, phenol, alkylphenol, catechol, alkylcatechol, hydroquinone, alkylhydroquinone, pyrogallol, phloroglycine, ureamelamine, urea, benzoguanamine, Polymers such as toluene, xylene, coumarin, cyclohexanone, cashew oil, tannins, Shichirank, Dammer, rosin-stomach gin derivatives, petroleum 11 fat, methanol, ethanol, isopropanol, N-butanol, ethylene glycol, glycerin, etc. Adding glycol, furfuryl alcohol, etc.
Co-condensation or modification is also acceptable. Further, a carbonyl group-containing compound such as acetone and pulllactam may be added as a condensation regulator.

上記初期縮合物と上記レゾルシノール系樹脂の他に第三
成分が添加されてもよψ。このような第三成分としては
天然ゴムおよびその誘導体、88R。
A third component may be added in addition to the above-mentioned initial condensate and the above-mentioned resorcinol resin. Such third components include natural rubber and its derivatives, 88R.

NBR,CB、EPR,ビニールビリジンター〆リマ一
等の合成ゴム、酢酸ビニル樹脂、エチレン・酢酸ビニル
共重合樹脂、アクリル樹脂、メタクリル樹脂、エチレン
・アクリル酸エステル共重合樹脂、塩化ビニル樹脂、塩
化ビニリデン樹脂、ポリスチレン、ポリエチレン、塩素
化ポリエチレン、ポリプロピレン、塩素化ポリプロピレ
ン、ポリエステル樹脂、ウレタン樹脂、ポリアミド、エ
ポキシ樹脂、ブチラール樹脂等の各種合成樹脂、ポリア
クリル醗塩、ポリアクリルアマイド、CMC1メチル七
ルローズ、ヒドロキシエチルセルローズ、ポリビニルア
ルコール、アルギン酸ソーダ、でん粉、でん粉誘導体、
ニカワ、ゼラチン、血粉のたん白質等の糊料、石こう、
炭酸カルシウム、カーボンブラック、木粉、クルミ粉、
ヤシガラ粉、小麦粉等の充填材、顔料(染料、難燃剤、
防虫剤、防腐剤、老化防止剤、紫外線吸収剤等がある。
Synthetic rubbers such as NBR, CB, EPR, Vinyl Vyridine Inter-Lima, vinyl acetate resin, ethylene/vinyl acetate copolymer resin, acrylic resin, methacrylic resin, ethylene/acrylic acid ester copolymer resin, vinyl chloride resin, vinylidene chloride Resin, polystyrene, polyethylene, chlorinated polyethylene, polypropylene, chlorinated polypropylene, polyester resin, urethane resin, polyamide, epoxy resin, various synthetic resins such as butyral resin, polyacrylic salt, polyacrylamide, CMC1 methyl heptylose, hydroxy Ethyl cellulose, polyvinyl alcohol, sodium alginate, starch, starch derivatives,
Glue, gelatin, glue such as blood meal protein, gypsum,
Calcium carbonate, carbon black, wood flour, walnut flour,
Coconut powder, fillers such as wheat flour, pigments (dyes, flame retardants,
There are insect repellents, preservatives, anti-aging agents, ultraviolet absorbers, etc.

上記初期縮合物ときレゾルシノール系樹脂との混合割合
社使用目的によって適宜調節せられるものであり、必ず
しも一律には限定されない。初期縮合物とレゾルシノー
ル系樹脂との混合割合により得られる接着剤の性質は変
化するが、初期縮合物の混合割合が大である場合は塩酸
、塩化アンモニウム、パラホルムアルデヒド等の醗性触
[の添加によって常温で硬化する接着剤となり、該接着
剤を合板の接着に用いれd合板JAs規格I類に合格す
る耐水接着性が容易に得られ、また初期縮合物かも生ず
るアルデヒドはレゾルシノール系樹脂に吸収されるから
遊離アルデヒド量が顕著に減少する。他方レゾルシノー
ル系樹脂の混合割合が大である場合は初期縮合物はレゾ
ルシノール系樹脂の硬化剤として機能するが、パラホル
ムアルデヒドを硬化剤として用−た場合よりも常温硬化
性が低く可使時間が長くなり、通常は加熱して硬化せし
めるがヘキサメチレンテシラミンを硬化剤として用いた
場合よりも低温短時間で硬化する。初基縮合物とレゾル
シノール系樹脂の混合割合がl:l近辺の場合は硬化剤
としてアルデヒドもしくはアルデヒド供与体を添加する
ことが望ましい。
The mixing ratio of the above-mentioned initial condensate and resorcinol resin can be appropriately adjusted depending on the purpose of use, and is not necessarily limited to a uniform ratio. The properties of the adhesive obtained vary depending on the mixing ratio of the initial condensate and resorcinol resin, but if the mixing ratio of the initial condensate is large, it is recommended to add a hydrochloric acid, ammonium chloride, paraformaldehyde, etc. This adhesive becomes an adhesive that hardens at room temperature, and when used to bond plywood, it is easy to obtain water-resistant adhesion that passes plywood JAs Standard Class I, and the aldehyde that may be generated as an initial condensation product is absorbed by the resorcinol resin. As a result, the amount of free aldehyde is significantly reduced. On the other hand, when the mixing ratio of resorcinol resin is large, the initial condensate functions as a curing agent for the resorcinol resin, but the room temperature curability is lower and the pot life is longer than when paraformaldehyde is used as a curing agent. Although it is usually cured by heating, it cures at a lower temperature and in a shorter time than when hexamethylenetecilamine is used as a curing agent. When the mixing ratio of the primary condensate and the resorcinol resin is around 1:1, it is desirable to add an aldehyde or an aldehyde donor as a curing agent.

上記したように本発明によって得られるエリア初期縮合
物とレゾルシノール系樹脂との混合物を主体とする接着
剤は両者の欠点が相補われ、適当なる可使時間を有する
とともに耐水性、耐煮沸性、耐候性に優れた接着を提供
するものであり、かくして該接着剤社木材、繊維、紙、
皮革、プラスチ体、金属−ガラス、陶磁器、コンクリー
ト等、汎〈有機、無機材料の接着に適用することが可能
である。
As described above, the adhesive mainly composed of a mixture of an area precondensate and a resorcinol resin obtained by the present invention compensates for the drawbacks of both, has an appropriate pot life, and is resistant to water, boiling, and weathering. This adhesive provides excellent adhesive properties for wood, fiber, paper,
It can be applied to bonding a wide range of organic and inorganic materials such as leather, plastic, metal-glass, ceramics, and concrete.

以下に本発明を更に具体的に説明するための実aaip
につ−て述べる。
The following is an actual aaip for explaining the present invention more specifically.
Let's talk about this.

実施例 エリア溶出物(ユリア含有量75重量%)100重量部
に37重重量%ルマリン203重量部と10重量鳴水酸
化ナトリウム水溶@/、j重量部を加え70℃、3時間
の加熱により不揮発分41J:/重量%、粘度4コボイ
ズ(Jjt’)、Pf17.$の初期縮合物を得る。
To 100 parts by weight of Example area eluate (urea content 75% by weight), 203 parts by weight of 37% by weight lumalin and 10 parts by weight of sodium hydroxide aqueous solution @/,j were added, and the mixture was non-volatile by heating at 70°C for 3 hours. min 41 J:/wt%, viscosity 4 coboise (Jjt'), Pf17. An initial condensate of $ is obtained.

レゾルシノール系樹脂としてはDFK−/NB(市販ア
ルキルレゾルシノール系樹脂二名古屋油化学工業株式会
社)を用−た。
As the resorcinol resin, DFK-/NB (commercially available alkyl resorcinol resin Ni Nagoya Yukagaku Kogyo Co., Ltd.) was used.

上記初期縮合物とDFK−/NBとを第1表に示す比率
に混合し、合板および集成材の接着剤として用−て性能
を評価した。その結果は第3表および第8表に示される
The above-mentioned initial condensate and DFK-/NB were mixed in the ratio shown in Table 1, and the mixture was used as an adhesive for plywood and laminated wood to evaluate its performance. The results are shown in Tables 3 and 8.

第   1   表 /、 ! −j −/、 !■のラワン材単板を用いて
3プライの合板を製造する。製造条件は次の通りである
Table 1/, ! −j −/, ! Manufacture 3-ply plywood using the lauan wood veneer from ■. The manufacturing conditions are as follows.

単板含水率    7〜to重量% 冷    圧     10#/dX/!分堆積時:1
間    S 分 熱    圧     lコ0℃X10kl/d×J分
接着剤塗布量     J j 9/900d上記のご
とくに製造した合板の接着性をJAS讐適合板の規格に
よって試験した。その結果を第3表に示す。
Veneer moisture content 7~towt% Cold pressure 10#/dX/! Minute accumulation time: 1
The adhesiveness of the plywood manufactured as described above was tested according to the JAS Compatible Board Standard. The results are shown in Table 3.

第E表にみるように初期縮合物とDFK−/NBとの混
合物At #Alは夫々の単独であるAI。
As shown in Table E, the mixture At #Al of the precondensate and DFK-/NB is each AI alone.

44に比してゲルタイム、即ち可使時間は長く、しか4
11IA返し煮沸後においても良好な接着性を示すが、
初期縮合物単独のム畠の場合は繰返し煮沸後におψて鉱
接着力が実質的に消失する。DFK−/NB単独のA4
は接着力にお―ては優れた耐煮沸性を示すがゲルタイム
が極めて短かψ。
Compared to 44, the gel time, that is, pot life is longer, but 4
11IA shows good adhesion even after boiling, but
In the case of the initial condensate alone, the ore adhesion force substantially disappears after repeated boiling. DFK-/NB alone A4
shows excellent boiling resistance in terms of adhesive strength, but the gel time is extremely short.

ベイマツ材を用いて集成材を製造する。製造条件は次の
通りである。
Manufacture laminated wood using Douglas fir wood. The manufacturing conditions are as follows.

含  水  率    、r−to重量%接着剤塗布量
   −,20g/II+’圧     締    ?
#/dXJjtX2#krz上記のごとく製造した集成
材の接着性をJIBK−4102によって試験した。そ
の結果を第8表に示す。
Moisture content, r-to weight% adhesive application amount -, 20g/II+'pressure?
#/dXJjtX2#krz The adhesiveness of the laminated wood produced as described above was tested according to JIBK-4102. The results are shown in Table 8.

1fsI     衣 第8表にみるように初期縮合物単独である&3は極めて
耐水性、耐煮沸性に劣るが、これにDFK−/Nを添加
したAI 、AIは耐水性、耐煮沸性が格段に向上して
いる。
1fsI Cloth As shown in Table 8, &3, which is an initial condensate alone, has extremely poor water resistance and boiling resistance, but AI and AI with DFK-/N added to it have significantly higher water resistance and boiling resistance. It's improving.

Claims (1)

【特許請求の範囲】[Claims] エリアを消失性物質として用−る精密鋳造法において生
ずるエリア溶出物にアルデヒドもしくはアルデヒド供与
体を添加し反応せしめてエリア初期縮合物となし、該エ
リア初期縮合物にレゾルシノール系樹脂を添加して接着
剤となすことを特徴とする精密鋳造法に用いたエリアの
再利用方法
Aldehyde or an aldehyde donor is added to the area eluate generated in the precision casting method that uses area as a fugitive substance and reacted to form an area initial condensate, and a resorcinol resin is added to the area initial condensate for bonding. A method for reusing the area used in precision casting, which is characterized by
JP14017781A 1981-09-04 1981-09-04 Method for reusing urea used in precision casting Pending JPS5849769A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14017781A JPS5849769A (en) 1981-09-04 1981-09-04 Method for reusing urea used in precision casting

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14017781A JPS5849769A (en) 1981-09-04 1981-09-04 Method for reusing urea used in precision casting

Publications (1)

Publication Number Publication Date
JPS5849769A true JPS5849769A (en) 1983-03-24

Family

ID=15262676

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14017781A Pending JPS5849769A (en) 1981-09-04 1981-09-04 Method for reusing urea used in precision casting

Country Status (1)

Country Link
JP (1) JPS5849769A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11510850A (en) * 1995-11-13 1999-09-21 ボーデン・ケミカル・インコーポレーテッド Compositions and methods for curing resorcinol resins

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11510850A (en) * 1995-11-13 1999-09-21 ボーデン・ケミカル・インコーポレーテッド Compositions and methods for curing resorcinol resins

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