JPH0913004A - Solidifying agent for solvent-based coating material - Google Patents

Solidifying agent for solvent-based coating material

Info

Publication number
JPH0913004A
JPH0913004A JP7168794A JP16879495A JPH0913004A JP H0913004 A JPH0913004 A JP H0913004A JP 7168794 A JP7168794 A JP 7168794A JP 16879495 A JP16879495 A JP 16879495A JP H0913004 A JPH0913004 A JP H0913004A
Authority
JP
Japan
Prior art keywords
solvent
resin
coating material
solidifying
paint
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.)
Granted
Application number
JP7168794A
Other languages
Japanese (ja)
Other versions
JP2866030B2 (en
Inventor
Ryuji Dobashi
隆二 土橋
Yoichi Maeyama
洋一 前山
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.)
Suzuka Fine Co Ltd
Original Assignee
Suzuka Fine Co Ltd
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 Suzuka Fine Co Ltd filed Critical Suzuka Fine Co Ltd
Priority to JP7168794A priority Critical patent/JP2866030B2/en
Publication of JPH0913004A publication Critical patent/JPH0913004A/en
Application granted granted Critical
Publication of JP2866030B2 publication Critical patent/JP2866030B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To obtain an agent which can quickly solidify a solvent-based coating material even when added thereto in a small amount and, is therefore useful in e.g. the disposal of a waste coating material by using an organometal alkoxide, a chelate compound or a coupling agent. SOLUTION: At least one compound selected from among organometal alkoxides (e.g. titanium alkoxide), chelate compounds (e.g. aluminum chelate) and coupling compounds (e.g. silicone coupling agent) is used as a solidifying agent for a solvent-based coating material (e.g. alkyd resin coating material). These compounds react with the carboxyl, hydroxyl or like groups of a solvent- based coating material and therefore have a function of effecting its thickening and gelation. It is also possible to produce a solidifying agent for a solvent-based coating material by using a polyisocyanate resin (e.g. hexamethylene diisocyanate) as the principal component. The polyisocyanate resin has a property of reacting the hydroxyl groups of the solvent-based coating material and solidifying it. Waste solvent-based coating materials are solidified by using these solidifying agents, and the solidified coating materials are disposed of.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は溶剤系塗料の固化剤に関
し、詳しくは、不要となった溶剤系塗料を固化して廃棄
する場合に用いるに適した固化剤に係わるものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a solidifying agent for solvent-based paints, and more particularly to a solidifying agent suitable for solidifying and discarding unnecessary solvent-based paints.

【0002】[0002]

【従来の技術】溶剤系塗料は、水系塗料のように、セメ
ント、酸化カルシウム、酸化マグネシウムによりほとん
ど固化させることができない。2液タイプのウレタン樹
脂塗料、エポキシ樹脂塗料、ポリエステル樹脂塗料など
は、基剤と硬化剤を混合した後、数時間経過すると固形
になるが、1液タイプの熱可塑性樹脂であるアルキド樹
脂塗料、アクリル樹脂塗料、アクリルアルキド樹脂塗
料、塩化ビニル樹脂塗料、塩化ゴム樹脂塗料などは溶剤
を完全に蒸発させないと固形物にできなかった。
2. Description of the Related Art Solvent-based paints, unlike water-based paints, can hardly be solidified by cement, calcium oxide and magnesium oxide. Two-component urethane resin coatings, epoxy resin coatings, polyester resin coatings, etc., become solid after a few hours have passed after the base and curing agent have been mixed, but one-component thermoplastic resin alkyd resin coatings, Acrylic resin paints, acrylic alkyd resin paints, vinyl chloride resin paints, chlorinated rubber resin paints, etc. could not be solidified unless the solvent was completely evaporated.

【0003】一方、廃油処理技術としては合成繊維、天
然繊維に廃油を吸着させる手段、廃油中に高級脂肪酸の
グリセライドおよびポリエチレン、パラフィンワックス
等を添加後、60℃以上の熱をかけ、溶解・冷却して固
化させる手段が知られている。繊維に吸着させる手段は
廃棄する多量の塗料を吸着できない。熱をかける手段
は、溶剤系塗料中に含まれる溶剤の引火点以上の温度に
加熱するため、引火の危険性がある。溶剤系塗料はその
まま廃棄すると、火災、土壊汚染、大気汚染の原因とな
るため、廃棄する場合は、専門の廃棄物処理業者にまか
せ、業者において溶剤系塗料を燃焼処理するか、あるい
は溶剤を除去し乾燥固化の処理を行なって、廃棄されて
いる。
On the other hand, as the waste oil treatment technology, synthetic fibers, means for adsorbing waste oil to natural fibers, glyceride of higher fatty acid, polyethylene, paraffin wax, etc. are added to the waste oil, and then heat and 60 ° C. or more are applied to melt and cool. A means for solidifying by doing is known. The means for adsorbing to the fiber cannot adsorb a large amount of the discarded paint. Since the means for applying heat heats to a temperature above the flash point of the solvent contained in the solvent-based paint, there is a risk of ignition. If you discard the solvent-based paint as it is, it may cause fire, soil pollution, and air pollution.If you dispose of it, leave it to a specialized waste disposal contractor and either burn the solvent-based paint or dispose of the solvent. It has been removed, dried and solidified, and discarded.

【0004】[0004]

【発明が解決しようとする課題】しかし、溶剤系塗料中
の溶剤を蒸発させるには、自然状態では、長時間を要
し、蒸発した溶剤成分の炭化水素類は大気中に、拡散し
て光化学スモッグなどの大気汚染の原因となる不都合が
ある。また専門の廃棄物処理業者にて、溶剤と樹脂・顔
料分などの固形物を分離する場合においても、かなりの
労力が必要となる。そこで、本発明の課題は、溶剤系塗
料を少量の添加で早期に固化できる固化剤を提供するこ
とにある。
However, in the natural state, it takes a long time to evaporate the solvent in the solvent-based paint, and the evaporated hydrocarbon component hydrocarbons diffuse into the atmosphere and photochemically react. There is an inconvenience that causes air pollution such as smog. In addition, a considerable amount of labor is required even when a specialized waste disposal company separates solid materials such as solvent and resin / pigment. Therefore, an object of the present invention is to provide a solidifying agent which can solidify a solvent-based paint early even by adding a small amount.

【0005】[0005]

【課題を解決するための手段】前記課題を解決するため
に、請求項1の発明は有機金属アルコキシド(通常、ア
ルコレ−トともいわれる。)あるいはキレ−ト(キレ−
ト化合物)あるいはカップリング化合物のいずれか1種
又は複数種を含むことを特徴とする。
In order to solve the above-mentioned problems, the invention of claim 1 provides an organometallic alkoxide (usually also called an alcoholate) or a chelate (a chelate).
Compound) or a coupling compound.

【0006】前記課題を解決するために、請求項2の発
明はポリイソシアネ−ト樹脂を主体としてなることを特
徴とする。
In order to solve the above-mentioned problems, the invention of claim 2 is characterized in that a polyisocyanate resin is mainly used.

【0007】前記課題を解決するために、請求項3の発
明は請求項2記載の固化剤100重量部(以下、単に部
と略記する。)と、水系塗料1〜50部とを含んでなる
ことを特徴とする。
In order to solve the above-mentioned problems, the invention of claim 3 comprises 100 parts by weight of the solidifying agent of claim 2 (hereinafter abbreviated as "part") and 1 to 50 parts of water-based paint. It is characterized by

【0008】前記課題を解決するために、請求項4の発
明はポリイソシアネ−ト樹脂1〜99部とポリオ−ル樹
脂1〜99部を含むことを特徴とする。
In order to solve the above-mentioned problems, the invention of claim 4 is characterized by containing 1 to 99 parts of a polyisocyanate resin and 1 to 99 parts of a polyol resin.

【0009】前記課題を解決するために、請求項5の発
明は請求項4記載の固化剤100部と、水及び水系塗料
の少くとも1種の1〜50部とを含んでなることを特徴
とする。
In order to solve the above-mentioned problems, the invention of claim 5 comprises 100 parts of the solidifying agent of claim 4 and 1 to 50 parts of at least one kind of water and water-based paint. And

【0010】溶剤系塗料とはアルキド樹脂塗料(合成樹
脂調合ペイント)、アクリル樹脂塗料、アクリルアルキ
ド樹脂塗料、塩化ゴム塗料、塩化ビニル樹脂塗料、エポ
キシエステル樹脂塗料、一液ウレタン樹脂塗料、フェノ
−ル樹脂塗料、油性塗料などが含まれる。請求項1にお
ける有機金属アルコキシド、キレ−ト、カップリング化
合物とは錯化合物などをさす。すなわち、チタンアシレ
−ト、チタンアルコキシド、チタンキレ−ト、チタンカ
ップリング剤、アルミニウムアルコキシド、アルミニウ
ムキレ−ト、シリコンカップリング剤など金属化合物で
あり、これらは溶剤系塗料中のカルボン酸、水酸基など
の酸基と反応し増粘・ゲル化する。溶剤系塗料に対する
これらの使用量は予じめのテストにより、適宜に定め得
る。
Solvent-based paints are alkyd resin paints (synthetic resin mixed paints), acrylic resin paints, acrylic alkyd resin paints, chlorinated rubber paints, vinyl chloride resin paints, epoxy ester resin paints, one-component urethane resin paints, phenols. Includes resin paints and oil paints. The organometallic alkoxide, the chelate, and the coupling compound in the first aspect refer to complex compounds and the like. That is, they are metal compounds such as titanium acylate, titanium alkoxide, titanium chelate, titanium coupling agent, aluminum alkoxide, aluminum chelate, and silicon coupling agent, and these are carboxylic acids in solvent-based paints and acids such as hydroxyl groups. Reacts with the base and thickens and gels. The amount of these used for the solvent-based paint can be appropriately determined by a preliminary test.

【0011】請求項2に係わるポリイソシアネ−ト樹脂
とは、MDI(フェニルメタンジイソシアネ−ト)およ
びプレポリマ−、XDI(キシリレンジイソシアネ−
ト)およびプレポリマ−、ヘキサメチレンジイソシアネ
−トなどの蒸気になりにくく安全で扱い易いものがあげ
られる。なお、TDI(トリレンジイソシアネ−ト)お
よびそのプレポリマ−は蒸気になり易く危険な特定化学
物質とされているため、取扱いに注意を要する。本発明
で用いるポリイソシアネ−ト樹脂は蒸気になりにくく作
業者に危険性の少い、取扱い易いものを使用することが
望ましい。
The polyisocyanate resin according to claim 2 means MDI (phenylmethane diisocyanate) and prepolymer, and XDI (xylylene diisocyanate).
And prepolymer, hexamethylene diisocyanate, etc., which are less likely to become vapor and are safe and easy to handle. In addition, TDI (tolylene diisocyanate) and its prepolymer are liable to become vapors and are specified as dangerous chemical substances. As the polyisocyanate resin used in the present invention, it is desirable to use a resin which does not easily become vapor and which is less dangerous to the operator and is easy to handle.

【0012】ポリイソシアネ−ト樹脂は反応基であるイ
ソシアネ−トを10%以上、30%以下含む樹脂を言
う。ポリイソシアネ−ト樹脂は、溶剤系塗料100部に
対して、1部以上50部以下が用いられる。1部以下の
場合は、溶剤系塗料との反応性が少なく、50部以上の
場合は、価格が高くなり、廃棄物処理業者に委託した方
が有利となる。ポリイソシアネ−ト樹脂とともに用いる
ポリオ−ル樹脂は、アクリルポリオ−ル、ポリエ−テル
ポリオ−ル、ポリエステルポリオ−ル、アルキドポリオ
−ル、エポキシポリオ−ルなど樹脂中に架橋性のある水
酸基を含有した樹脂である。本発明に使用するポリオ−
ル樹脂はポリイソシアネ−ト樹脂との反応性が速く、硬
化時間が60分以内の樹脂が好ましい。
The polyisocyanate resin means a resin containing 10% or more and 30% or less of isocyanate which is a reactive group. The polyisocyanate resin is used in an amount of 1 part or more and 50 parts or less with respect to 100 parts of the solvent-based paint. When the amount is 1 part or less, the reactivity with the solvent-based paint is low, and when the amount is 50 parts or more, the price becomes high, and it is advantageous to entrust a waste treatment company. Polyol resin used together with polyisocyanate resin is a resin containing a crosslinkable hydroxyl group in the resin such as acrylic polyol, polyether polyol, polyester polyol, alkyd polyol and epoxy polyol. Is. Polio used in the present invention
The resin has a high reactivity with the polyisocyanate resin, and a resin having a curing time of 60 minutes or less is preferable.

【0013】水系塗料とは、アクリル、アクリルスチレ
ン、酢酸ビニル、塩化ビニル樹脂などを単独または複数
共重合したエマルションを使用した水系塗料、あるいは
水を含む水性塗料が含まれる。本発明では残材とする水
系塗料を使用することができ、ポリイソシアネ−ト樹脂
の架橋促進に使用する。エマルション塗料などの水系塗
料を添加する効果としては、ポリイソシアネ−ト樹脂の
架橋性を上げることを目的に用いる。1部以下の場合
は、量的に不足して架橋性が少なく、50部以上の場合
はポリイソシアネ−ト樹脂など架橋が不足し、水が分離
し、固化が遅れる。なお、請求項1〜請求項5の各発明
には、亜鉛華などの着色顔料、炭酸カルシウムなどの体
質顔料を30部以下量において配合することができる。
本発明の固化材の塗料に対する添加量は1%以上が好ま
しい。1%より少ない場合は固化までの時間が必要であ
り、塗料により固化しない場合が考えられる。
The water-based coating material includes water-based coating material using an emulsion obtained by copolymerizing acrylic, acrylic styrene, vinyl acetate, vinyl chloride resin, etc., alone or in a plurality thereof, or water-based coating material containing water. In the present invention, a water-based paint as a residual material can be used and is used to accelerate the crosslinking of the polyisocyanate resin. As an effect of adding an aqueous paint such as an emulsion paint, it is used for the purpose of increasing the crosslinkability of the polyisocyanate resin. If the amount is 1 part or less, the amount is insufficient and the crosslinkability is low. If the amount is 50 parts or more, the polyisocyanate resin or the like is insufficiently crosslinked, water is separated, and solidification is delayed. In each of the first to fifth aspects of the invention, a color pigment such as zinc white and an extender pigment such as calcium carbonate can be added in an amount of 30 parts or less.
The addition amount of the solidifying material of the present invention to the coating material is preferably 1% or more. When it is less than 1%, it takes time to solidify, and it may be considered that the paint does not solidify.

【0014】請求項1、請求項2の固化剤はその主成分
を使用単位の容器に詰めることにより製品とすることが
できる。請求項4の固化剤は所定の二成分の所定量を各
々別容器に分けて入れ、これを一セットとすることで製
品となし得る。請求項3の固化剤はポリイソシアネ−ト
樹脂と、水系塗料との、所定の混合量を容器に分けて入
れ、一セットとすることで使用現場で扱い易い形態とす
ることができる。請求項5の固化剤はポリイソシアネ−
ト樹脂と、ポリオ−ル樹脂と、水及び水系塗料及びエマ
ルション塗料のいずれか1種との、所定の混合量を各々
別容器に分けて入れ、一セットとすることにより使用現
場で扱い易い形態とすることができる。上記した各固化
剤の製品は、使用し易いものであり、直に使用しない場
合は、反応性を保つために密閉した形態とすることが望
ましい。
The solidifying agent of claims 1 and 2 can be made into a product by packing the main component of the solidifying agent into a container of a unit of use. The solidifying agent of claim 4 can be made into a product by putting predetermined amounts of the predetermined two components in separate containers and setting them as one set. The solidifying agent of the third aspect can be made into a form that can be easily handled at the site of use by dividing a predetermined amount of the polyisocyanate resin and the water-based paint into a container and putting them in one set. The solidifying agent according to claim 5 is polyisocyanate.
The resin resin, the polyol resin, and any one of water, water-based paint, and emulsion paint are put in separate containers and put in separate containers, so that one set can be easily handled at the site of use. Can be The above-mentioned products of the respective solidifying agents are easy to use, and when they are not used directly, it is desirable that they are in a sealed form in order to maintain reactivity.

【0015】[0015]

【作用】各請求項における主たる作用は次の如くであ
る。請求項1においては、有機金属アルコキシド、ある
いはキレ−ト、あるいはカップリング化合物が、溶剤系
塗料の成分と反応し、溶剤系塗料の固化作用をなす。請
求項2においては、ポリイソシアネ−ト樹脂が溶剤系塗
料の水酸基と反応し、溶剤系塗料を固化させる。請求項
3においては、ポリイソシアネ−ト樹脂が水系塗料の水
分、あるいは溶剤系塗料の水酸基と反応し、溶剤系塗料
を固化させる。請求項4においては、ポリイソシアネ−
ト樹脂がポリオ−ル樹脂と反応の際に溶剤系塗料がとり
込まれて固化される。請求項5においては、ポリイソシ
アネ−ト樹脂がポリオ−ル樹脂、あるいは水、あるいは
水系塗料の水分、あるいはエマルション塗料の水分、及
び溶剤系塗料の水酸基と反応し、溶剤系塗料を固化させ
る。
The main action in each claim is as follows. In the first aspect, the organic metal alkoxide, the chelate, or the coupling compound reacts with the components of the solvent-based paint to solidify the solvent-based paint. In the second aspect, the polyisocyanate resin reacts with the hydroxyl groups of the solvent-based paint to solidify the solvent-based paint. In the third aspect, the polyisocyanate resin reacts with the water content of the water-based paint or the hydroxyl group of the solvent-based paint to solidify the solvent-based paint. In claim 4, polyisocyanate
When the resin reacts with the polyol resin, the solvent-based paint is incorporated and solidified. In the fifth aspect, the polyisocyanate resin reacts with the polyol resin, water, water of the water-based paint, water of the emulsion paint, and hydroxyl groups of the solvent-based paint to solidify the solvent-based paint.

【0016】[0016]

【実施例】次に、本発明の各実施例を説明する。実施例
1は有機金属アルコキシドよりなる固化剤、実施例2及
び実施例3はキレ−トよりなる固化剤、実施例4はカッ
プリング化合物よりなる固化剤であり、この各実施例は
単独成分のみよりなる。この実施例1〜4は請求項1の
発明に対応する。
EXAMPLES Next, examples of the present invention will be described. Example 1 is a solidifying agent made of an organometallic alkoxide, Examples 2 and 3 are solidifying agents made of chelate, and Example 4 is a solidifying agent made of a coupling compound. Each of these Examples is a single component. Consists of. Examples 1 to 4 correspond to the invention of claim 1.

【0017】実施例1のアルコキシドは川研ファインケ
ミカル(株)製造の商品名「アルミニウムアルコレ−ト
ASBD」を使用し、実施例2のキレ−トは川研ファイ
ンケミカル(株)製造の商品名「アルミニウムキレ−ト
ALCH」、及び実施例3のキレ−トは味の素(株)製
造の商品名「チタンキレ−トKR−41B」を各単独で
使用し、前記カップリング化合物は味の素(株)製造の
商品名「プレンアクトKR TTS」を使用した。
The alkoxide used in Example 1 was "Aluminum alcohol ASBD" manufactured by Kawaken Fine Chemical Co., Ltd., and the chelate used in Example 2 was "Aluminum manufactured by Kawaken Fine Chemical Co., Ltd.""ChelateALCH" and the chelate of Example 3 are the product names "Titanium chelate KR-41B" manufactured by Ajinomoto Co., Inc., which are used alone, and the coupling compound is a product manufactured by Ajinomoto Co., Inc. The name "Plenact KR TTS" was used.

【0018】一方、比較例1としては市販の繊維系吸油
材である、カクイ(株)製造の商品名「カポック繊維カ
クイオイルキャッチャ−」を用意し、比較例2は市販の
オイル固め剤である、ジョンソン(株)製造の商品名
「テンプル」を用意した。
On the other hand, as Comparative Example 1, a commercially available fiber oil absorbing material, "Kapok Fiber Kakui Oil Catcher" manufactured by Kakui Co., Ltd. is prepared, and Comparative Example 2 is a commercially available oil solidifying agent. "Temple" manufactured by Johnson Co., Ltd. was prepared.

【0019】本例1〜4及び比較例1、2は各々溶剤系
塗料に添加し混合して固化試験を行った。固化試験のた
めの溶剤系塗料は、アクリル樹脂塗料としてラフトンア
クリエナメル、アクリルアルキド樹脂塗料としてアクリ
ルバ−ン、合成樹脂調合ペイントとしてエスコ−トホ−
プDXを用いた。なお、ラフトンアクリエナメル、アク
リルバ−ン及びエスコ−トホ−プDXはいずれもスズカ
ファイン(株)製造の市販品である。
Each of Examples 1 to 4 and Comparative Examples 1 and 2 was added to a solvent-based paint and mixed to carry out a solidification test. Solvent-based paints for the solidification test were Ruffton Acryenamel as acrylic resin paint, acrylic vane as acrylic alkyd resin paint, and Escort hoat as synthetic resin compounding paint.
DX was used. Rafton Acrynamel, Acrylic Burn, and Escort Hop DX are all commercial products manufactured by Suzuka Fine Co., Ltd.

【0020】溶剤系塗料は各1kgに対し、室温20℃
において、本例1〜4の固化剤のいずれかを10g(塗
料に対する外割%として1%に相当)、30g(塗料に
対する外割%として3%に相当)、50g(塗料に対す
る外割%として5%に相当)、添加し混合した。次いで
固化剤を混合した塗料は温度20℃、湿度70%RHの
雰囲気(以下、所定の雰囲気という。)中に放置して固
化時間及び固化状態を調べた。固化時間の判定は溶剤系
塗料が固形状となり、触れたときに塗料成分が手に付か
なくなった時間を目安とした。固化時間の確認は実用
上、96時間を限度として判定し、96時間内で固化で
きないものは不良としてその評価を×印とした。比較例
1、2の固化試験は各溶剤系塗料に対し、使用説明にし
たがって使用した。本例1〜4及び比較例1、2の固化
試験の結果は表1に示すとおりであった。
For each 1 kg of solvent-based paint, room temperature is 20 ° C.
In any of the solidifying agents of Examples 1 to 4, 10 g (corresponding to 1% as an outer percentage of the paint), 30 g (equivalent to 3% as an outer percentage of the paint), 50 g (as an outer percentage of the paint) 5%) and added and mixed. Next, the coating material mixed with the solidifying agent was left in an atmosphere (hereinafter, referred to as a predetermined atmosphere) having a temperature of 20 ° C. and a humidity of 70% RH, and the solidifying time and the solidified state were examined. The determination of the solidification time was based on the time when the solvent-based paint became solid and the paint components could not be touched when touched. Practical confirmation of the solidification time was judged within a limit of 96 hours, and those which could not be solidified within 96 hours were judged to be defective and the evaluation was marked x. The solidification tests of Comparative Examples 1 and 2 were used for each solvent-based paint according to the instruction for use. The results of the solidification tests of Examples 1 to 4 and Comparative Examples 1 and 2 are shown in Table 1.

【0021】[0021]

【表1】 (表1中、本例1〜4欄における各数値単位は時間であ
る。以下の各固化試験の結果の表においても同様であ
る。)
[Table 1] (In Table 1, each numerical unit in the first to fourth columns of the present example is time. The same applies to the following table of results of each solidification test.)

【0022】表1により明らかなように本例1〜4の固
化剤はいずれも96時間以内で溶剤系塗料を固化させる
ことができたが、比較例1、2は固化できなかった。な
お、本例1〜4の固化物の性状は使用した本例の溶剤系
塗料にかかわらず、おおよそ次の如くであった。本例1
では小さな顆粒状となった。本例2及び本例3、本例4
では軟質で大きな顆粒状となった。
As is clear from Table 1, all of the solidifying agents of Examples 1 to 4 were able to solidify the solvent-based paint within 96 hours, but Comparative Examples 1 and 2 could not. The properties of the solidified products of Examples 1 to 4 were approximately as follows regardless of the solvent-based paint used in this example. Example 1
It became a small granular form. Example 2 and Example 3 and Example 4
The result was soft and large granules.

【0023】実施例5及び実施例6はポリイソシアネ−
ト樹脂の単独成分よりなる固化剤であり、請求項2の発
明に対応するものである。実施例5のポリイソシアネ−
ト樹脂は日本ポリウレタン(株)製造の商品名MDI系
「コロネ−ト2067」を用い、実施例6のポリイソシ
アネ−ト樹脂は日本ポリウレタン(株)製造の商品名H
MDI系「コロネ−トHX」を用いた。本例5及び本例
6は溶剤系塗料(ラフトンアクリエナメル、アクリルバ
−ン、エスコ−トホ−プDX)に添加して固化試験を行
った。
Examples 5 and 6 are polyisocyanates.
It is a solidifying agent consisting of a single component of resin and corresponds to the invention of claim 2. Polyisocyanate of Example 5
The resin used is MDI type "Coronet 2067" manufactured by Nippon Polyurethane Co., Ltd., and the polyisocyanate resin of Example 6 is manufactured by Nippon Polyurethane Co., Ltd.
MDI system "Coronet HX" was used. In Example 5 and Example 6, solidification tests were carried out by adding them to solvent-based paints (Rafton Acryenamel, acrylic burn, Escort Hop DX).

【0024】溶剤系塗料は各1kgに対して、本例5及
び本例6の固化剤のいずれか100g(塗料に対する外
割%として10%に相当)、300g(塗料に対する外
割%として30%に相当)添加し混合した。固化剤を混
合した塗料は所定の雰囲気中に放置して固化時間及び固
化状態を調べた。固化時間の判定は前記した実施例の場
合と同様とし、96時間内で固化しないものは不良(×
印)とした。本例5及び本例6の固化試験の結果は、表
2に示すとおりであった。
For each 1 kg of solvent-based paint, 100 g (corresponding to 10% as an outer percentage of the paint) of the solidifying agent of Examples 5 and 6 and 300 g (30% as an outer percentage of the paint) Equivalent to) and mixed. The coating material mixed with the solidifying agent was left in a predetermined atmosphere to examine the solidifying time and the solidified state. The solidification time was determined in the same manner as in the above-described examples, and those that did not solidify within 96 hours were defective (x
Mark). The results of the solidification tests of Examples 5 and 6 are shown in Table 2.

【0025】[0025]

【表2】 [Table 2]

【0026】表2より明らかなように、本例5、6の固
化剤の10%添加量において、アクリルバ−ン(アクリ
ルアルキッド樹脂塗料)及びエスコ−トホ−プDX(合
成樹脂調合ペイント)は96時間内に固化させることが
できたが、ラフトンアクリエナメル(アクリル樹脂塗
料)は固化できなかった。本例5、6の固化剤の30%
添加量においてはラフトンアクリエナメル、アクリルバ
−ン及びエスコ−トホ−プDXを96時間内に固化させ
ることができた。なお、本例5、6の固化物の性状はい
ずれも顆粒状のものとなった。
As is clear from Table 2, 96% of acrylic burn (acrylic alkyd resin paint) and Escort Hop DX (synthetic resin blend paint) were added at 10% of the solidifying agent of Examples 5 and 6. It was possible to solidify within the time, but Rafton Acryenamel (acrylic resin paint) could not be solidified. 30% of the solidifying agent of Examples 5 and 6
In terms of the amount added, Rafton acryl enamel, acrylic burn and Escort Hop DX could be solidified within 96 hours. The properties of the solidified products of Examples 5 and 6 were both granular.

【0027】実施例7及び実施例8は、ポリイソシアネ
−ト樹脂とエマルション塗料の2成分よりなる固化剤で
あり、請求項3の発明に対応する。ポリイソシアネ−ト
樹脂は前記したMDI系の「コロネ−ト2067」及び
前記HMDI系の「コロネ−トHX」とし、エマルショ
ン塗料はスズカファイン(株)製造の商品名「AEP6
000」を用いた。実施例7及び実施例8の各固化剤2
成分は表3に示す割合とした。
Examples 7 and 8 are solidifying agents comprising two components, a polyisocyanate resin and an emulsion paint, and correspond to the invention of claim 3. The polyisocyanate resin is the above-mentioned MDI-based "Coronet 2067" and the above-mentioned HMDI-based "Coroneto HX", and the emulsion paint is trade name "AEP6" manufactured by Suzuka Fine Co., Ltd.
000 ”was used. Each solidifying agent 2 of Example 7 and Example 8
The components are in the proportions shown in Table 3.

【0028】[0028]

【表3】 (表3中の配合量単位は部である。)[Table 3] (The compounding amount unit in Table 3 is part.)

【0029】次いで、本例7及び8の固化剤を用いて、
溶剤系塗料(ラフトンアクリエナメル、アクリルバ−
ン、エスコ−トホ−プDX)の固化試験を行った。溶剤
系塗料は各1kgに対して、本例7及び本例8の固化剤
のいずれか100g(塗料に対する外割%として10%
に相当)、300g(塗料に対する外割%として30%
に相当)添加し混合した。固化剤を混合した塗料は所定
の雰囲気中に放置して固化時間及び固化状態を調べた。
固化時間の判定は前記した実施例の場合と同様とし、9
6時間内で固化しないものは不良(×印)とした。本例
7、8の固化試験の結果は表4に示すとおりであった。
Then, using the solidifying agents of Examples 7 and 8,
Solvent-based paint (Rafton Acryenamel, acrylic bar
, Escort Hop DX). For each 1 kg of solvent-based paint, 100 g of either one of the solidifying agents of Examples 7 and 8 (10% as an outer percentage of the paint)
Equivalent to), 300g (30% as an external percentage of the paint)
Equivalent to) and mixed. The coating material mixed with the solidifying agent was left in a predetermined atmosphere to examine the solidifying time and the solidified state.
The determination of the solidification time is the same as in the case of the above-mentioned embodiment, and 9
Those that did not solidify within 6 hours were regarded as defective (x mark). The results of the solidification tests of Examples 7 and 8 are shown in Table 4.

【0030】[0030]

【表4】 [Table 4]

【0031】表4より明らかなように、本例7、8の固
化剤は、いずれも0.3時間以内で溶剤系塗料を固化さ
せることができた。なお、本例7、8の固化物の性状
は、いずれも顆粒状となった。
As is clear from Table 4, the solidifying agents of Examples 7 and 8 were able to solidify the solvent-based paint within 0.3 hours. The properties of the solidified products of Examples 7 and 8 were both granular.

【0032】実施例9及び実施例10の固化剤はポリオ
−ル樹脂とポリイソシアネ−ト樹脂との2成分よりなる
ものであり、請求項4の発明に対応する。ポリオ−ル樹
脂としては大成化工(株)製造のアクリルポリオ−ル樹
脂の商品名「アクリット6XC−006」及び旭電化工
業(株)製造のエポキシポリオ−ル樹脂の商品名「アデ
カレジンEP6075」を用い、ポリイソシアネ−ト樹
脂としては日本ポリウレタン(株)製造の商品名MDI
系「コロネ−ト2067」を用いた。実施例9及び実施
例10の各固化剤2成分は表5に示す割合とした。
The solidifying agents of Examples 9 and 10 are composed of two components, a polyol resin and a polyisocyanate resin, and correspond to the invention of claim 4. As the polyol resin, the trade name "Acryt 6XC-006" of acrylic polyol resin manufactured by Taisei Kako Co., Ltd. and the trade name "ADEKA RESIN EP6075" of epoxy polyol resin manufactured by Asahi Denka Co., Ltd. were used. , The polyisocyanate resin is MDI manufactured by Nippon Polyurethane Co., Ltd.
The system "Coronet 2067" was used. The proportions of the two solidifying agent components of Example 9 and Example 10 were set as shown in Table 5.

【0033】[0033]

【表5】 (表5中の配合量単位は部である。)[Table 5] (The compounding unit in Table 5 is part.)

【0034】本例9及び本例10はラフトンアクリエナ
メル(溶剤系塗料)に添加して固化試験を行った。溶剤
系塗料は各1kgに対して、本例9及び本例10のいず
れかを100g(塗料に対する外割%として10%)、
300g(塗料に対する外割%として30%)添加混合
した。固化剤を混合した塗料は所定の雰囲気中に放置し
て固化時間及び固化状態を調べた。固化時間の判定は前
記と同様とし、96時間内で固化できないものは不良
(×印)とした。本例9及び本例10の固化試験の結果
は表6に示すとおりであった。
In Examples 9 and 10, the solidification test was carried out by adding to Rafton Acryenamel (solvent-based paint). For each 1 kg of solvent-based paint, 100 g of either Example 9 or Example 10 (10% as an outer percentage of the paint),
300 g (30% as an outer percentage of the paint) was added and mixed. The coating material mixed with the solidifying agent was left in a predetermined atmosphere to examine the solidifying time and the solidified state. The determination of the solidification time was the same as described above, and those that could not be solidified within 96 hours were regarded as defective (marked with X). The results of the solidification tests of Examples 9 and 10 are shown in Table 6.

【0035】[0035]

【表6】 [Table 6]

【0036】表6より明らかなように、本例9、10の
固化剤は、いずれも7時間以内でラフトンアクリエナメ
ル(アクリル樹脂塗料)を固化させることができた。な
お、本例9、10の固化物の性状は、いずれも顆粒状の
ものとなった。
As is clear from Table 6, all of the solidifying agents of Examples 9 and 10 were able to solidify the Rafton acryl enamel (acrylic resin paint) within 7 hours. The properties of the solidified products of Examples 9 and 10 were all granular.

【0037】実施例11、実施例12、実施例13及び
実施例14は、ポリイソシアネ−ト樹脂とポリオ−ル
と、エマルション塗料あるいは水との3成分よりなる固
化剤であり、請求項5の発明に対応する。
Examples 11, 12, 13, and 14 are solidifying agents consisting of three components, a polyisocyanate resin, a polyol, and an emulsion paint or water. Corresponding to.

【0038】ポリイソシアネ−ト樹脂はMDI系の「コ
ロネ−ト2067」とし、ポリオ−ル樹脂は「アクリッ
ト6XC−006」及び「アデカレジンEP6075」
とし、エマルション塗料は「AEP6000」を用い
た。実施例11乃至14の各固化剤の3成分は表7に示
す割合とした。
The polyisocyanate resin is MDI type "Coronet 2067", and the polyol resin is "Acryt 6XC-006" and "Adeka Resin EP6075".
The emulsion paint used was "AEP6000". The ratios of the three components of each solidifying agent of Examples 11 to 14 are shown in Table 7.

【0039】[0039]

【表7】 (表7中の配合量単位は部である。)この本例11乃至
14の固化剤を用いて、溶剤系塗料(ラフトンアクリエ
ナメル)の固化試験を行った。
[Table 7] (The unit of the compounding amount in Table 7 is part.) A solidification test of a solvent-based paint (Rafton Acrynamel) was conducted using the solidifying agents of the present Examples 11 to 14.

【0040】溶剤系塗料は各1kgに対して、本例11
乃至本例14の固化剤のいずれかを100g(塗料に対
する外割%として10%に相当)、300g(塗料に対
する外割%として30%に相当)添加し混合した。固化
剤を混合した塗料は所定の雰囲気中に放置して固化時間
及び固化状態を調べた。固化時間の判定は前記した各実
施例の場合と同様とし、96時間内で固化しないものは
不良(×印)とした。本例11乃至14の固化試験の結
果は表8に示すとおりであった。
For each 1 kg of solvent-based paint, this Example 11
Or, 100 g (corresponding to 10% of the outer percentage of the paint) or 300 g (corresponding to 30% of the outer percentage of the paint) of any of the solidifying agents of Example 14 was added and mixed. The coating material mixed with the solidifying agent was left in a predetermined atmosphere to examine the solidifying time and the solidified state. The determination of the solidification time was made in the same manner as in each of the above-mentioned Examples, and those which did not solidify within 96 hours were regarded as defective (marked with X). The results of the solidification tests of Examples 11 to 14 are shown in Table 8.

【0041】[0041]

【表8】 [Table 8]

【0042】表9に示すように、本例11乃至14の固
化剤は、いずれも6時間以内でラフトンアクリエナメル
(溶剤系塗料)を固化させることができた。なお、本例
11乃至14の固化物の性状は、いずれも顆粒状のもの
となった。
As shown in Table 9, all of the solidifying agents of Examples 11 to 14 were able to solidify Rafton Acryenamel (solvent-based paint) within 6 hours. The properties of the solidified products of Examples 11 to 14 were all granular.

【0043】[0043]

【発明の効果】請求項1乃至請求項5の発明によれば、
従来の吸油剤に較べ、溶剤系塗料に対したとえば1〜3
0の外割%という少量の添加量で、たとえば96時間以
内の早期に溶剤系塗料を固化することができる。したが
って、本発明の固化剤を使用すれば使用後の余った溶剤
系塗料、あるいは不要となった溶剤系塗料を固化物とし
て廃棄する場合に都合がよい。請求項1乃至請求項5の
各固化剤は、溶剤系塗料に少量添加することにより、溶
剤系塗料を粉末あるいは顆粒状に固化させることがで
き、この固化物は産業廃棄物、廃プラスチックとして処
理することができる。なお、請求項3あるいは請求項5
の発明によれば、水系塗料を固化成分となし得ることよ
り不要の水系塗料を溶剤系塗料とともに短時間に固化さ
せることができて都合がよい。
According to the first to fifth aspects of the present invention,
Compared to conventional oil absorbing agents, for solvent-based paints, for example, 1 to 3
With a small addition amount of 0%, it is possible to solidify the solvent-based paint early, for example, within 96 hours. Therefore, the use of the solidifying agent of the present invention is convenient when the excess solvent-based paint after use or the unnecessary solvent-based paint is discarded as a solidified product. By adding a small amount of each of the solidifying agents of claims 1 to 5 to the solvent-based paint, the solvent-based paint can be solidified into powder or granules, and the solidified product is treated as industrial waste or waste plastic. can do. In addition, claim 3 or claim 5
According to the invention of (1), since the water-based paint can be used as a solidifying component, the unnecessary water-based paint can be solidified together with the solvent-based paint in a short time, which is convenient.

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 有機金属アルコキシドあるいはキレ−ト
あるいはカップリング化合物のいずれか1種又は複数種
を含むことを特徴とした溶剤系塗料の固化剤。
1. A solidifying agent for a solvent-based coating material, which comprises any one or a plurality of organometallic alkoxides, chelates or coupling compounds.
【請求項2】 ポリイソシアネ−ト樹脂を主体としてな
ることを特徴とした溶剤系塗料の固化剤。
2. A solidifying agent for a solvent-based paint, which is mainly composed of a polyisocyanate resin.
【請求項3】 請求項2記載の固化剤100重量部と、
水系塗料1〜50重量部とを含んでなることを特徴とし
た溶剤系塗料の固化剤。
3. 100 parts by weight of the solidifying agent according to claim 2,
A solidifying agent for a solvent-based paint, comprising 1 to 50 parts by weight of a water-based paint.
【請求項4】 ポリイソシアネ−ト樹脂1〜99重量部
とポリオ−ル樹脂1〜99重量部を含むことを特徴とし
た溶剤系塗料の固化剤。
4. A solidifying agent for a solvent-based paint, comprising 1 to 99 parts by weight of a polyisocyanate resin and 1 to 99 parts by weight of a polyol resin.
【請求項5】 請求項4記載の固化剤100重量部と、
水及び水系塗料の少くとも1種の1〜50重量部とを含
んでなることを特徴とした溶剤系塗料の固化剤。
5. 100 parts by weight of the solidifying agent according to claim 4,
A solidifying agent for a solvent-based paint, comprising 1 to 50 parts by weight of water and at least one kind of water-based paint.
JP7168794A 1995-07-04 1995-07-04 Solidifying agent for solvent-based paint Expired - Fee Related JP2866030B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7168794A JP2866030B2 (en) 1995-07-04 1995-07-04 Solidifying agent for solvent-based paint

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7168794A JP2866030B2 (en) 1995-07-04 1995-07-04 Solidifying agent for solvent-based paint

Publications (2)

Publication Number Publication Date
JPH0913004A true JPH0913004A (en) 1997-01-14
JP2866030B2 JP2866030B2 (en) 1999-03-08

Family

ID=15874603

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7168794A Expired - Fee Related JP2866030B2 (en) 1995-07-04 1995-07-04 Solidifying agent for solvent-based paint

Country Status (1)

Country Link
JP (1) JP2866030B2 (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01102085A (en) * 1987-09-23 1989-04-19 Giulini Chem Gmbh Novel aluminum-magnesium-hydroxy compound and manufacture
JPH03137101A (en) * 1989-06-05 1991-06-11 Aqualon Co Siliconized polysaccharide

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01102085A (en) * 1987-09-23 1989-04-19 Giulini Chem Gmbh Novel aluminum-magnesium-hydroxy compound and manufacture
JPH03137101A (en) * 1989-06-05 1991-06-11 Aqualon Co Siliconized polysaccharide

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