JPS58224750A - Manufacture of melamine-resin decorative material - Google Patents

Manufacture of melamine-resin decorative material

Info

Publication number
JPS58224750A
JPS58224750A JP10884582A JP10884582A JPS58224750A JP S58224750 A JPS58224750 A JP S58224750A JP 10884582 A JP10884582 A JP 10884582A JP 10884582 A JP10884582 A JP 10884582A JP S58224750 A JPS58224750 A JP S58224750A
Authority
JP
Japan
Prior art keywords
carbonic acid
resin
decorative material
molding
melamine
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
JP10884582A
Other languages
Japanese (ja)
Inventor
尾畑 佳紀
岩田 照徳
隆志 神谷
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.)
Aica Kogyo Co Ltd
Original Assignee
Aica Kogyo 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 Aica Kogyo Co Ltd filed Critical Aica Kogyo Co Ltd
Priority to JP10884582A priority Critical patent/JPS58224750A/en
Publication of JPS58224750A publication Critical patent/JPS58224750A/en
Pending legal-status Critical Current

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  • Laminated Bodies (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Reinforced Plastic Materials (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明はメラミン樹脂化粧材の製法に関するものである
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a melamine resin decorative material.

従来、メラミン樹脂化粧板はメラミン樹脂を化粧紙に含
浸した表面層用シートと石炭酸ホルムアルデヒド樹脂(
以下石炭酸樹脂という)をクラフト紙等に含浸したコア
層用シートとを積層し熱圧成型していた。しかしながら
石炭酸樹脂の硬化に長時間を要し、成型サイクルが長く
なって生産性が劣っていた。従って当然連続成型は全く
不可能であった。
Traditionally, melamine resin decorative boards have been made using a surface layer sheet made by impregnating decorative paper with melamine resin and a carbonate formaldehyde resin (
A core layer sheet made of kraft paper or the like impregnated with carbonic acid resin (hereinafter referred to as carbonic acid resin) was laminated and hot-press molded. However, it took a long time to harden the carbonic acid resin, resulting in a long molding cycle and poor productivity. Naturally, therefore, continuous molding was completely impossible.

本発明は上知の問題点を解決したメラミン樹脂化粧材の
製法に係り、更に詳しくはメラミン樹脂をオーバーレイ
紙、化粧紙等に含浸した表面層用シートとクラフト紙等
の基材に石炭酸樹脂の硬化速度を向上せしめた変性石炭
酸ホルムアルデヒド樹脂(以下変性石炭酸樹脂という)
を含浸処理して作成したコア層用シートとを積層し熱圧
成型することを特徴とするメラミン樹脂化粧材の製法に
関するものである。
The present invention relates to a method for producing a melamine resin decorative material that solves the known problems. Modified carbonic acid formaldehyde resin with improved curing speed (hereinafter referred to as modified carbonic acid resin)
The present invention relates to a method for producing a melamine resin decorative material, which comprises laminating a sheet for a core layer prepared by impregnating the melamine resin with a core layer sheet and then hot-pressing the same.

該変性石炭酸樹脂としては、mクレゾール、pクレゾー
ル、3.5キシレノール、3.4キシレノール、レゾル
シノール、2.5キシレノール等の石炭酸よシも反応硬
化速度の速い各種フェノール類と石炭酸とを共縮合する
か、石炭酸樹脂にこれら各種フェノール類とホルムアル
デヒドとの反応物質とを混合してなるものが使用できる
The modified carbonic acid resin is prepared by co-condensing various phenols with a fast reaction curing rate, such as m-cresol, p-cresol, 3.5-xylenol, 3.4-xylenol, resorcinol, and 2.5-xylenol. Alternatively, a mixture of carbonic acid resin and a reactant of these various phenols and formaldehyde can be used.

石炭酸と各種フェノール類とを共縮合させるには石炭酸
と各種フェノール類との混合物にホルムアルデヒドを投
入し、弱アルカリ下で加熱しつつ継続して反応させ適度
な反応終点にて冷却し合、成するか、特に反応の速いフ
ェノール類では石炭酸とホルムアルデヒドとの反ら途中
にフェノール類を徐々に添加しつつ反応させたのち、適
性な反応終点で冷却し合成することができる。また場合
によっては個別に合成した石炭酸樹脂と各種フェノール
類から合成した各種フェノール類・・ホルムア・ルデヒ
ド樹脂とを混合させた変性石炭酸樹脂も使用できる。変
性石炭酸樹脂の共縮合比率ないし混合比率は目的とする
成型体の物性、成型条件ならびに使用する各種フェノー
ル類の種類に対応して決定される。
To co-condense carbolic acid and various phenols, formaldehyde is added to a mixture of carbolic acid and various phenols, the reaction is continued while heating under a weak alkali, and the mixture is cooled at the appropriate end point of the reaction. Alternatively, phenols that react particularly quickly can be synthesized by gradually adding the phenol during the reaction between carbolic acid and formaldehyde, and then cooling at an appropriate end point of the reaction. In some cases, a modified carbonic acid resin obtained by mixing individually synthesized carbonic acid resin with various phenol-formaldehyde resins synthesized from various phenols can also be used. The co-condensation ratio or mixing ratio of the modified carbonic acid resin is determined depending on the physical properties of the intended molded product, molding conditions, and the type of various phenols used.

更に石炭酸樹脂、変性石炭酸、\樹:脂はホルムアルデ
ヒドとの反応モル比、pH(−例′:えば苛性ソーダ、
炭酸す) IJウム量等)、反応触媒の種類及び添加i
Kより反応硬化速度が促進されるため、必要に応じてp
H調整(例えば苛性ソーダ量の調整)するかあるいけ、
アニリンm (p)−フェニレンジアミン、m (p)
−アミノフェノール、o(pi)ルイジン、エチレンジ
アミン、ジエチレントリアミン、ジアミノジフェニルメ
タン類等の反応触媒ないしこれらにパラフォルムアルデ
ヒドを添加した複合反応触媒等を添加することにより成
型硬化性を向上せしめることができる。
Furthermore, the reaction molar ratio of the carbonic acid resin, modified carbonic acid, \resin:resin with formaldehyde, pH (for example, caustic soda,
carbonic acid), amount of IJum, etc.), type and addition of reaction catalyst
Since the reaction curing rate is faster than K, p may be added as necessary.
Do you want to adjust H (e.g. adjust the amount of caustic soda)?
Aniline m(p)-phenylenediamine, m(p)
-Mold curability can be improved by adding a reaction catalyst such as -aminophenol, o(pi)luidine, ethylenediamine, diethylenetriamine, diaminodiphenylmethane, or a composite reaction catalyst in which paraformaldehyde is added to these.

該メラミンレジン及び該変性石炭酸樹脂がαセルロース
センイ、クラフトセンイ、リンターセンイ等の天然セン
イ、ビニロン、ナイロン、アクリル等の合成センイある
いはガラスセンイ、石綿センイ等の無機センイないしこ
れらの混在センイ等から作られた紙、布、不織布等の多
孔質基材に塗工ないし含浸等手段により保持されて含浸
紙等の成型素材が作られる。
The melamine resin and the modified carbonic acid resin may be made from natural fibers such as α-cellulose fiber, craft fiber, linter fiber, synthetic fibers such as vinylon, nylon, acrylic, inorganic fibers such as glass fiber, asbestos fiber, or mixtures thereof. A molded material such as impregnated paper is produced by applying or impregnating the resin onto a porous base material such as paper, cloth, or nonwoven fabric.

本発明は前記の通りメラミン樹脂化粧材の成型ザイクル
船縮ならびに連続成型化を目的としたものであり、次に
連続成型する成型法の1例について述べると、例えば第
1図はその1手段として採用する成型装置の概要図であ
って、同一方向へ平行に連続的に走行する2枚のエンド
レスベルト(5)(5)間に表面層用シート(4)及び
コア層用シート(B)とが連続的に挿入され、核酸型装
置に付設されている加熱板(ロ)よシなる加熱手段及び
圧縮空気により加圧する加圧手段によシ、連続的に加熱
加圧できる機構になっている0該加熱板(ロ)には加熱
オイルあるいは水蒸気が循環していて、250℃以゛下
であれば、°任意温度に設定でき、しかも圧力調節器に
より圧力1〜25”9/、1間で所定圧力に調節できる
ので、一定熱圧条件下で連続成型できる。
As mentioned above, the purpose of the present invention is to achieve cycle shrinkage and continuous molding of melamine resin decorative materials. Next, an example of a continuous molding method will be described. For example, FIG. This is a schematic diagram of the molding device employed, in which a surface layer sheet (4) and a core layer sheet (B) are placed between two endless belts (5) (5) that run continuously in parallel in the same direction. is inserted continuously, and is capable of being heated and pressurized continuously using a heating means such as a heating plate (b) attached to the nucleic acid device and a pressurizing means that pressurizes with compressed air. 0 Heating oil or steam is circulated through the heating plate (b), and the temperature can be set to any desired temperature as long as it is below 250°C, and the pressure can be adjusted between 1 and 25"9/1 with a pressure regulator. Since the pressure can be adjusted to a predetermined value, continuous molding is possible under constant heat and pressure conditions.

またエンドレスペル) (505)の走行速度、加熱温
度の設定によシメラミン樹脂及びコア層の成型条件に対
応できる。該メラミン樹脂化粧材の表面に凹凸エンボス
を設けるには、該エンドレスヘルドにエッチンク加工シ
タスチールエンドレスベルト、あるいはステンレスエン
ドレスベルトを使用したシ、エンドレスベルトと宍面層
用シートの間に成型条件に耐用するエンボス紙、エンボ
ス樹脂シート、織布、エンボス金属シート等の賦型シー
トを挿入すれば、これら凹凸エンボス面が転写成型でき
る。
Also, by setting the running speed and heating temperature of Endrespel (505), it is possible to correspond to the molding conditions of the simelamine resin and the core layer. In order to provide uneven embossing on the surface of the melamine resin decorative material, use an etched steel endless belt or a stainless steel endless belt on the endless heald, and use a material that can withstand the molding conditions between the endless belt and the sheet for the Shishimen layer. By inserting a forming sheet such as embossed paper, embossed resin sheet, woven fabric, or embossed metal sheet, these uneven embossed surfaces can be transferred and molded.

なお連続成型には上記の成型のほか、回転する成型ドラ
ムに金属製エンドレスベルトを押し付けながら成型する
ドラム成型法、連続ロール間で加熱加圧して連続成型す
る連続ロール法等の方法が採用できる。
In addition to the above-mentioned molding methods, continuous molding methods can be used such as a drum molding method in which a metal endless belt is pressed against a rotating molding drum, and a continuous roll method in which continuous molding is performed by heating and pressurizing between continuous rolls.

本発明になるメラミン樹脂化粧材の製法によれば、従来
高圧プレスにて、長時間の成型工程で作業していたもの
が、成型時間が著しく短縮され成型能率が顕著に向上で
きる。また加熱時間が短縮されるため省エネルギーが達
成されると同時に、連続成型によれば含浸紙等の成型材
料を自動的に連続して成型機に挿入するものであるため
に、従来ノバッチグレスにおいて必要であった含浸紙等
の積層準備(セット)工程が不要となり省力化も達成さ
れた。
According to the method for producing a melamine resin decorative material according to the present invention, the molding time, which conventionally required a long molding process using a high-pressure press, can be significantly shortened and molding efficiency can be significantly improved. In addition, energy saving is achieved because the heating time is shortened, and at the same time, with continuous molding, molding materials such as impregnated paper are automatically and continuously inserted into the molding machine, which is not necessary in conventional Nobachi Gress. The process of preparing for lamination (setting) of impregnated paper, etc., which was previously required, was no longer necessary, and labor savings were also achieved.

実施例、比較例 米坪il:50”/mのαセルロース紙に硬化剤を含む
反応モル比1.5のメラミン樹脂を樹脂率180%含浸
処理して表面層用シートとし、米坪量120f/n? 
 のクラフト紙に石炭酸と各種フェノール類とを共縮合
させた変性石炭酸樹脂を樹脂率60%含浸処理してコア
層用シー)A−C作成し、石炭酸樹脂に各種フェノール
類ホルムアルデヒド樹脂を混合した変性石炭酸樹脂を同
一クラフト紙に樹脂率60チ含浸処理してコア層用シー
トDSEを作成し、各コア層用シート3枚に該表面層用
シート1枚を積層し実施例のメラミン樹脂化粧材(イ)
〜(ホ)を成型した。また比較例として石炭酸樹脂を実
施例と同一のクラフト紙に樹脂率60チ含浸処理してコ
ア層用シートを作成し、このシート3枚の上に該表面層
用シート1枚を積層し比較例のメラミン樹脂化粧材(へ
)を成型した。成型条件及び試験結果は第1表の通シで
ある。
Examples and Comparative Examples α-cellulose paper with a basis weight of 50”/m was impregnated with a melamine resin containing a curing agent and a reaction molar ratio of 1.5 at a resin rate of 180% to form a sheet for the surface layer. /n?
Craft paper is impregnated with 60% resin ratio of modified carbonic acid resin, which is a co-condensation of carbonic acid and various phenols, to create core layer sheets A-C, and modified carbonic acid resin is mixed with various phenolic formaldehyde resins. A sheet DSE for the core layer was prepared by impregnating the same kraft paper with a resin ratio of 60%, and one sheet for the surface layer was laminated on three sheets for each core layer to obtain the melamine resin decorative material of the example ( stomach)
~(E) was molded. In addition, as a comparative example, a sheet for the core layer was prepared by impregnating the same kraft paper as in the example with a resin ratio of 60%, and one sheet for the surface layer was laminated on three of these sheets. A melamine resin decorative material was molded. The molding conditions and test results are as shown in Table 1.

(8) 01り注 煮沸水中に30分間放置し、フクレ、ハクリ
等の発生しない成型品が得られた成型時間
(8) Note 01: Molding time when a molded product without blistering, peeling, etc. was obtained after being left in boiling water for 30 minutes.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明に係る連続成型機の1例概要図、第2図
は連続成型機の他側概要図である。 1.9・・・・テンションロール 2・・・・駆動ロール  3・・・・加圧室4・・・・
コンプレッサー 5.10・・・・エンドレスベ゛(4 6・・・・シール材   7・・・・成型ドラム8.8
′・・・・圧着ロール 11・・・・加熱板12.12
′・・・・油圧シリンダー 13.13′・・・・成型化粧材 特許出願人  アイカニ業株式会社
FIG. 1 is a schematic diagram of one example of a continuous molding machine according to the present invention, and FIG. 2 is a schematic diagram of the other side of the continuous molding machine. 1.9... Tension roll 2... Drive roll 3... Pressure chamber 4...
Compressor 5.10... Endless bay (4 6... Seal material 7... Molding drum 8.8
'...Crimping roll 11...Heating plate 12.12
′・・・Hydraulic cylinder 13.13′・・・Molded decorative material patent applicant Aikanigyo Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] (11石炭酸及び石炭酸よりも反応速度の速い各種フェ
ノール類とホルムアルデヒドとを反応させた変性石炭酸
ホルムアルデヒド樹脂、あるいは石炭酸ホルムアルデヒ
ド樹脂及び各種フェノール類ホルムアルデヒド樹脂とを
混合した変性石炭酸ホルムアルデヒド樹脂を含浸処理し
てなるコア層用シートを使用することを特徴とするメラ
ミン樹脂化粧材の製法0(2)連続的に成型する特許請
求の範囲第1項記載のメラミン樹脂化粧材の製法。
(11 Impregnated with modified carbonic acid formaldehyde resin made by reacting formaldehyde with various phenols having a reaction rate faster than carbonic acid, or modified carbonic acid formaldehyde resin mixed with carbonic acid formaldehyde resin and various phenolic formaldehyde resins) A method for manufacturing a melamine resin decorative material characterized by using a core layer sheet 0(2) A method for manufacturing a melamine resin decorative material according to claim 1, which involves continuous molding.
JP10884582A 1982-06-24 1982-06-24 Manufacture of melamine-resin decorative material Pending JPS58224750A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10884582A JPS58224750A (en) 1982-06-24 1982-06-24 Manufacture of melamine-resin decorative material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10884582A JPS58224750A (en) 1982-06-24 1982-06-24 Manufacture of melamine-resin decorative material

Publications (1)

Publication Number Publication Date
JPS58224750A true JPS58224750A (en) 1983-12-27

Family

ID=14495037

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10884582A Pending JPS58224750A (en) 1982-06-24 1982-06-24 Manufacture of melamine-resin decorative material

Country Status (1)

Country Link
JP (1) JPS58224750A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0447940A (en) * 1990-06-15 1992-02-18 Matsushita Electric Works Ltd Production of multilayer printed wiring board

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0447940A (en) * 1990-06-15 1992-02-18 Matsushita Electric Works Ltd Production of multilayer printed wiring board

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