JP6344612B2 - Manufacturing method of high gloss decorative board - Google Patents
Manufacturing method of high gloss decorative board Download PDFInfo
- Publication number
- JP6344612B2 JP6344612B2 JP2015073212A JP2015073212A JP6344612B2 JP 6344612 B2 JP6344612 B2 JP 6344612B2 JP 2015073212 A JP2015073212 A JP 2015073212A JP 2015073212 A JP2015073212 A JP 2015073212A JP 6344612 B2 JP6344612 B2 JP 6344612B2
- Authority
- JP
- Japan
- Prior art keywords
- seconds
- resin composition
- paper
- weight
- decorative
- 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.)
- Active
Links
Landscapes
- Finished Plywoods (AREA)
- Laminated Bodies (AREA)
Description
本発明は、基材の少なくとも一方の表面にメラミン樹脂系被覆層を積層して熱圧成型するメラミン系樹脂化粧板の製造法に関する。 The present invention relates to a method for producing a melamine-based resin decorative board in which a melamine resin-based coating layer is laminated on at least one surface of a substrate and hot-press molded.
従来の高光沢メラミン化粧板の製造方法としては、図柄印刷を施して得られた化粧紙に熱硬化性樹脂を含浸処理、乾燥して得られるプリプレグをクラフト含浸紙に重ね合わせて高圧(例えば50〜120kg/cm2)にて熱圧成型することにより積層体とし、さらにこの積層体を接着剤で基材表面に接着する方法が行われている。この方法で得られる製品は高圧メラミン化粧板と呼ばれている。 As a conventional method for producing a high-gloss melamine decorative board, a decorative paper obtained by pattern printing is impregnated with a thermosetting resin, and a prepreg obtained by drying is superimposed on a kraft-impregnated paper to apply high pressure (for example, 50 A method is employed in which a laminate is formed by hot-press molding at ˜120 kg / cm 2 ), and this laminate is further adhered to the substrate surface with an adhesive. The product obtained by this method is called a high-pressure melamine decorative board.
しかしながら、この製造法は、高い光沢を備えた製品が得られるものの、含浸紙とクラフト含浸紙を積層するのに長時間のプレス処理を必要とし、さらに接着面をサンディングしたのち、接着剤にて基材へ接着するなど工程数が多いという欠点がある。
更に、基材にパーチクルボード、MDF、合板などの木質系基材を用いる場合、プレスによる厚み減りの問題があり、高圧をかけることができない基材がある。
However, although this manufacturing method can provide a product with high gloss, it requires a long press process to laminate impregnated paper and kraft impregnated paper, and after sanding the adhesive surface, There is a drawback that the number of steps is large, such as bonding to a substrate.
Furthermore, when using a woody base material such as particle board, MDF, or plywood as the base material, there is a problem of thickness reduction due to pressing, and there is a base material on which high pressure cannot be applied.
そこで、クラフト含浸紙との積層を行うことなしに、未硬化の含浸化粧紙を直接基材に重ね合わせると同時にプレス成型する方法が採用されている。この方法は短時間で化粧板までの大量生産が可能で、この方法で得られる製品はショートサイクルメラミン化粧板もしくは低圧メラミン化粧板と呼ばれる。 Therefore, a method is employed in which uncured impregnated decorative paper is directly superimposed on a base material and simultaneously press-molded without being laminated with kraft impregnated paper. This method enables mass production up to a decorative board in a short time, and the product obtained by this method is called a short cycle melamine decorative board or a low-pressure melamine decorative board.
しかし、低圧メラミン化粧板は高圧メラミン化粧板と比較し、光沢の低いもの、艶消し製品に限定されてしまう。その原因としては例えば短時間に含浸樹脂を硬化させるので、含浸紙と基材の成型は高温で行われ、ホットプレスから取り出されるために、含浸紙及び木質基材が含有する水分や、熱硬化性樹脂の縮合反応で生じる脱離生成物が、成型材料表面で抜け出す過程で光沢低下等の表面性状の悪化を招きやすいためとされている。
そのため、高圧をかけることができない木質系基材を用いた化粧板は、表面の光沢が低い半艶程度であったり、高い光沢と低い艶の混ざった艶ムラを生じたりして安定して高い光沢の化粧板を作ることが難しい。現在、市場を流通している木質系基材を用いたショートサイクルメラミン化粧板は艶消しのものに限定されている。
However, the low-pressure melamine decorative board is limited to those having a low gloss and a matte product as compared with the high-pressure melamine decorative board. For example, the impregnated resin is cured in a short time, so the impregnated paper and the base material are molded at a high temperature and removed from the hot press. It is said that the desorption product produced by the condensation reaction of the functional resin tends to cause deterioration of the surface properties such as gloss reduction in the process of coming off on the surface of the molding material.
Therefore, a decorative board using a wooden base material that cannot be subjected to high pressure is stable and high, with a semi-glossy surface with a low surface gloss or uneven gloss with a mixture of high and low gloss. It is difficult to make a glossy decorative board. Currently, short-cycle melamine decorative boards using a wood-based base material on the market are limited to matte ones.
ショートサイクルメラミン化粧板の製造における上述の問題点を解決する手段としては、基材や含浸紙の揮発成分量を少なくする方法や含浸樹脂中の熱硬化樹脂量及び触媒量を増やす方法などがあるが、効果は十分ではない。特に後者は成型時のピンホールやクラックを招き、製品の表面性状を悪くし易い。
また、ショートサイクルメラミン化粧板の光沢を向上させる手段として、フタル酸ジアリルを必須成分とするミクロゲルエマルションを配合する方法が記載されている。この方法で製造された化粧板は、優れた光沢性を示すが、ミクロゲルエマルションが容易に入手出来ず、コスト的に高価となり、また添加量の制約がある等の問題点がある(特許文献1参照)。
Means for solving the above-mentioned problems in the production of a short cycle melamine decorative board include a method of reducing the amount of volatile components of the base material and impregnated paper, and a method of increasing the amount of thermosetting resin and catalyst in the impregnated resin. But the effect is not enough. In particular, the latter causes pinholes and cracks at the time of molding and tends to deteriorate the surface properties of the product.
In addition, as a means for improving the gloss of a short cycle melamine decorative board, a method of blending a microgel emulsion containing diallyl phthalate as an essential component is described. The decorative board produced by this method exhibits excellent gloss, but the microgel emulsion is not readily available, is expensive in terms of cost, and has a problem that the amount of addition is limited (Patent Document 1). reference).
そこで、本発明の課題は、含浸紙を基材に直接接着すると同時に成型を行う化粧板製造法(ショートサイクル法)において、高圧メラミン化粧板に匹敵する光沢と鮮映性を有する化粧板が得られる製造方法を提供することにある。 Accordingly, an object of the present invention is to obtain a decorative board having gloss and sharpness comparable to that of a high-pressure melamine decorative board in a decorative board manufacturing method (short cycle method) in which an impregnated paper is directly bonded to a substrate and simultaneously molded. It is to provide a manufacturing method.
メラミン樹脂を化粧紙に含浸、乾燥して得られるプリプレグを基材に重ね合わせ、加熱下で圧力を加えて、樹脂を硬化させると共に化粧紙を基材に接着する化粧板の製造法において、ゲルタイムの異なるメラミン樹脂組成物を用いて化粧紙を含浸することにより上記の課題を解決することできることを見出した。
即ち、本発明は以下のように記載することができる。
項1 メラミン樹脂を化粧紙に含浸、乾燥して得られるプリプレグを基材に重ね合わせ、加熱下で圧力を加えて、樹脂を硬化させると共に化粧紙を基材に接着する化粧板の製造法において、
ゲルタイムが120秒以上250秒以下であるメラミン樹脂組成物を、化粧紙に含浸する工程(紙間強化含浸工程)、及び
ゲルタイムが150秒以上400秒以下であるメラミン樹脂組成物を、紙間強化含浸工程を経た化粧紙に含浸する工程(本含浸工程)により、メラミン樹脂を化粧紙に含浸し、以下の式を満たすことを特徴とする化粧板の製造法。
本含浸工程におけるメラミン樹脂組成物のゲルタイム(秒)−紙間強化含浸工程におけるメラミン樹脂組成物のゲルタイム(秒)≧30(秒)
項2 基材がパーチクルボード、MDF(中密度繊維板)、ケナフボード、ベニヤ合板から選択される木質系基材、アルミニウム板、ステンレス板から選択される金属板系基材、酸化マグネシウム、水酸化アルミニウム、酸化アルミニウム、酸化ケイ素、酸化チタン、塩化マグネシウム、珪酸カルシウム、火山性ガラス質材料、石膏(硫酸カルシウム)、石灰石(炭酸カルシウム)、水硬性セメントおよび気硬性セメントの群から選択される少なくとも1種の材料を硬化させた無機質系基材のいずれかであることを特徴とする項1に記載の化粧板の製造法。
項3 JIS Z 8741に規定されている方法で測定した20度グロス値が100以上の化粧板であることを特徴とする項1又は2に記載の化粧板の製造法。
項4 ゲルタイムが120秒以上250秒以下であるメラミン樹脂組成物を、化粧紙に含浸する工程(紙間強化含浸工程)、及び
ゲルタイムが150秒以上400秒以下であるメラミン樹脂組成物を、紙間強化含浸工程を経た化粧紙に含浸する工程(本含浸工程)により、メラミン樹脂を化粧紙に含浸し、以下の式を満たすことを特徴とするプリプレグの製造法。
本含浸工程におけるメラミン樹脂組成物のゲルタイム(秒)−紙間強化含浸工程におけるメラミン樹脂組成物のゲルタイム(秒)≧30(秒)
Gel time in a method for producing a decorative board in which a prepreg obtained by impregnating and drying a melamine resin on a decorative paper is superimposed on a base material, and pressure is applied under heating to cure the resin and bond the decorative paper to the base material. It has been found that the above-mentioned problems can be solved by impregnating decorative paper with different melamine resin compositions.
That is, the present invention can be described as follows.
Item 1 In a method for producing a decorative board in which a prepreg obtained by impregnating and drying a decorative paper with melamine resin is superimposed on a base material, and pressure is applied under heating to cure the resin and bond the decorative paper to the base material. ,
A step of impregnating decorative paper with a melamine resin composition having a gel time of 120 seconds or more and 250 seconds or less (inter-paper reinforcing impregnation step), and a melamine resin composition having a gel time of 150 seconds or more and 400 seconds or less, A method for producing a decorative board, wherein a decorative paper subjected to an impregnation step is impregnated with a melamine resin by a step of impregnating the decorative paper (main impregnation step), and the following formula is satisfied.
Gel time (seconds) of melamine resin composition in this impregnation step-Gel time (seconds) of melamine resin composition in inter-paper reinforced impregnation step ≧ 30 (seconds)
Item 2 Base material is particle board selected from particle board, MDF (medium density fiberboard), kenaf board, veneer plywood, metal plate base material selected from aluminum plate, stainless steel plate, magnesium oxide, aluminum hydroxide , Aluminum oxide, silicon oxide, titanium oxide, magnesium chloride, calcium silicate, volcanic glassy material, gypsum (calcium sulfate), limestone (calcium carbonate), hydraulic cement and pneumatic cement Item 2. The method for producing a decorative board according to Item 1, which is any one of inorganic base materials obtained by curing the material.
Item 3 The method for producing a decorative board according to Item 1 or 2, wherein the decorative board has a 20-degree gloss value of 100 or more measured by a method defined in JIS Z 8741.
Item 4 A step of impregnating a decorative paper with a melamine resin composition having a gel time of 120 seconds or more and 250 seconds or less (inter-paper reinforcing impregnation step), and a melamine resin composition having a gel time of 150 seconds or more and 400 seconds or less, A method for producing a prepreg characterized by impregnating decorative paper with melamine resin through a step of impregnating decorative paper that has undergone an intertempering impregnation step (this impregnation step) and satisfying the following formula.
Gel time (seconds) of melamine resin composition in this impregnation step-Gel time (seconds) of melamine resin composition in inter-paper reinforced impregnation step ≧ 30 (seconds)
本発明の製造法により、一般的なショ−トサイクルメラミン化粧板の製造方法、成型条件で、高圧メラミン化粧板に匹敵する高い光沢と高い鮮映性、良好な平滑性を備えた化粧板の製造が可能になる。 According to the production method of the present invention, a general short-cycle melamine decorative board can be produced with a high gloss, high sharpness and good smoothness comparable to those of a high-pressure melamine decorative board under molding conditions and molding conditions. Manufacturing becomes possible.
以下、本発明の製造法について詳述する。
本発明はメラミン樹脂を化粧紙に含浸、乾燥して得られるプリプレグを基材に重ね合わせ、加熱下で圧力を加えて、樹脂を硬化させると共に化粧紙を基材に接着する化粧板の製造法(ショートサイクル法)に関するものである。
Hereinafter, the production method of the present invention will be described in detail.
The present invention relates to a method for producing a decorative board in which a prepreg obtained by impregnating and drying decorative paper with melamine resin is laminated on a base material, and pressure is applied under heating to cure the resin and bond the decorative paper to the base material. (Short cycle method).
プリプレグ
本発明のプリプレグはメラミン樹脂を化粧紙に含浸、乾燥して得られるが、ゲルタイムの異なるメラミン樹脂組成物を用いて化粧紙を含浸することを特徴とする。即ち、先にゲルタイムの短いメラミン樹脂組成物を紙間の奥に浸透させ(紙間強化含浸工程とも記載する)、紙間強化含浸工程を経た化粧紙に紙間強化含浸工程に用いたメラミン樹脂組成物よりもゲルタイムの長いメラミン樹脂組成物を用いて含浸する(本含浸工程とも記載する)ことを特徴とする。
Prepreg The prepreg of the present invention is obtained by impregnating decorative paper with melamine resin and drying, and is characterized by impregnating decorative paper with melamine resin compositions having different gel times. That is, the melamine resin used in the inter-paper strengthening impregnation step on the decorative paper that has previously been impregnated with the melamine resin composition having a short gel time into the back of the paper (also referred to as inter-paper strengthening impregnation step). Impregnation is performed using a melamine resin composition having a longer gel time than the composition (also referred to as this impregnation step).
本発明のメラミン樹脂組成物に使用されるメラミン樹脂は高圧成型用メラミン樹脂でもかまわないが、低圧成型用メラミン樹脂が好ましい。メラミン樹脂としてはメラミン及びその誘導体をモノマーとする樹脂であれば公知のものを採用することができ、単一のモノマーからなる樹脂であってもよく、複数のモノマーからなる共重合体であってもよい。メラミンの誘導体としては、例えば、イミノ基やメチロール基、メトキシメチル基、ブトキシメチル基等のアルコキシメチル基などの官能基を有する誘導体が挙げられる。また、メチロール基を有するメラミン誘導体に低級アルコールを反応させて部分的あるいは完全にエーテル化した化合物をモノマーとして用いることもできる。 The melamine resin used in the melamine resin composition of the present invention may be a melamine resin for high pressure molding, but a melamine resin for low pressure molding is preferred. As the melamine resin, a known resin can be adopted as long as it is a resin having melamine and its derivatives as monomers, and it may be a resin composed of a single monomer or a copolymer composed of a plurality of monomers. Also good. Examples of the melamine derivative include derivatives having a functional group such as an alkoxymethyl group such as an imino group, a methylol group, a methoxymethyl group, or a butoxymethyl group. A compound obtained by reacting a lower alcohol with a melamine derivative having a methylol group and partially or completely etherified can also be used as a monomer.
本発明のメラミン樹脂組成物においては、メラミン樹脂以外の樹脂を含有していてもよく、メチレングリコシド、ブチレングリコシド等のアルキレングリコシド樹脂、アクリル樹脂等を例示することができる。 In the melamine resin composition of the present invention, a resin other than the melamine resin may be contained, and examples thereof include alkylene glycoside resins such as methylene glycoside and butylene glycoside, acrylic resins, and the like.
本発明のメラミン樹脂組成物において、メラミン樹脂以外の樹脂を含有する場合には、樹脂成分におけるメラミン樹脂の比率は、50重量%以上であることが好ましく、70重量%以上であることがより好ましい。 In the melamine resin composition of the present invention, when a resin other than the melamine resin is contained, the ratio of the melamine resin in the resin component is preferably 50% by weight or more, and more preferably 70% by weight or more. .
本発明のメラミン樹脂組成物には、溶剤を用いてもよく、水、メタノール、エタノール、イソプロパノール等の水溶性有機溶剤が挙げられる。水と水溶性有機溶剤との混合物を使用してもよい。 In the melamine resin composition of the present invention, a solvent may be used, and examples thereof include water-soluble organic solvents such as water, methanol, ethanol, and isopropanol. A mixture of water and a water-soluble organic solvent may be used.
本発明のメラミン樹脂組成物には、硬化性触媒を用いてもよく特に限定されないが、塩化アンモニウム、p−トルエンスルホン酸、p−トルエンスルホン酸アンモニウム、イミドジスルホン酸ジアンモニウム、2−アミノ−2−メチル−1−プロパノール等を例示することができる。 A curable catalyst may be used in the melamine resin composition of the present invention, and is not particularly limited. However, ammonium chloride, p-toluenesulfonic acid, ammonium p-toluenesulfonate, diammonium imidodisulfonate, 2-amino-2 -Methyl-1-propanol etc. can be illustrated.
本発明のメラミン樹脂組成物には、必要に応じ、結晶性セルロース、硬化促進剤、離型剤、無機または有機の充填剤、可塑剤、分散剤、増粘剤、粘度調整剤、消泡剤、防腐剤、紫外線吸収剤、減耗剤、抗菌剤、レベリング剤等の通常使用される添加剤を含んでいてもよい。 If necessary, the melamine resin composition of the present invention includes crystalline cellulose, a curing accelerator, a release agent, an inorganic or organic filler, a plasticizer, a dispersant, a thickener, a viscosity modifier, and an antifoaming agent. Ordinarily used additives such as preservatives, ultraviolet absorbers, depleting agents, antibacterial agents, and leveling agents may be included.
本発明のメラミン樹脂組成物のゲルタイムは、硬化性触媒の種類、及び量、また、要すれば硬化性促進剤の種類、及び量が大きく影響を与えるものの、樹脂組成物全体の配合物、配合量によって、決定される。尚、メラミン樹脂組成物のゲルタイムは、5mlのメラミン樹脂組成物を直径16.5mm、長さ165mmのガラス製試験管にサンプリングし、その表面が容量約3Lの沸騰水の液面下約3cmになるように固定し、樹脂液が透明から白濁するまでの時間(秒)を測定する。 Although the gel time of the melamine resin composition of the present invention is greatly affected by the type and amount of the curable catalyst, and if necessary, the type and amount of the curable accelerator, the formulation and formulation of the entire resin composition Determined by quantity. The gel time of the melamine resin composition was 5 ml of melamine resin composition sampled into a glass test tube having a diameter of 16.5 mm and a length of 165 mm, and the surface was about 3 cm below the surface of boiling water having a capacity of about 3 L. And measure the time (seconds) until the resin liquid turns from transparent to cloudy.
本発明の化粧紙としては、チタン紙、薄葉紙、強化紙、クラフト紙、セルロース紙等の含浸用紙布、ポリエステル、レーヨン、アクリル、ビニロン等の不織布等が挙げられる。 Examples of the decorative paper of the present invention include impregnated paper cloth such as titanium paper, thin paper, reinforced paper, kraft paper, and cellulose paper, and nonwoven fabric such as polyester, rayon, acrylic, and vinylon.
紙間強化含浸工程
本発明の紙間強化含浸工程は、化粧紙にゲルタイムが120秒以上250秒以下であるメラミン樹脂組成物を含浸する。メラミン樹脂組成物は、ゲルタイムが120秒以上200秒以下であるメラミン樹脂組成物であることが好ましく、ゲルタイムが120秒以上195秒以下であるメラミン樹脂組成物であることが特に好ましい。
Inter-paper reinforcing impregnation step In the inter-paper reinforcing impregnation step of the present invention, a decorative paper is impregnated with a melamine resin composition having a gel time of 120 seconds or more and 250 seconds or less. The melamine resin composition is preferably a melamine resin composition having a gel time of 120 seconds to 200 seconds, and particularly preferably a melamine resin composition having a gel time of 120 seconds to 195 seconds.
含浸温度は10〜35℃であることが好ましく、20〜30℃であることがより好ましい。 The impregnation temperature is preferably 10 to 35 ° C, and more preferably 20 to 30 ° C.
本含浸工程
本発明の本含浸工程は、紙間強化含浸工程を経た化粧紙にゲルタイムが150秒以上400秒以下であるメラミン樹脂組成物を含浸する。メラミン樹脂組成物は、ゲルタイムが190秒以上350秒以下であるメラミン樹脂組成物であることが好ましく、ゲルタイムが195秒以上300秒以下であるメラミン樹脂組成物であることが特に好ましい。
Main impregnation step In the main impregnation step of the present invention, the decorative paper that has undergone the inter-paper reinforcing impregnation step is impregnated with a melamine resin composition having a gel time of 150 seconds to 400 seconds. The melamine resin composition is preferably a melamine resin composition having a gel time of 190 seconds to 350 seconds, and particularly preferably a melamine resin composition having a gel time of 195 seconds to 300 seconds.
含浸温度は10〜35℃であることが好ましく、20〜30℃であることがより好ましい。 The impregnation temperature is preferably 10 to 35 ° C, and more preferably 20 to 30 ° C.
本含浸工程で得られた含浸された化粧紙は、乾燥させることにより、本発明のプリプレグとなる。乾燥温度は120〜160℃であることが好ましく、130〜150℃であることがより好ましい。 The impregnated decorative paper obtained in this impregnation step becomes the prepreg of the present invention by drying. The drying temperature is preferably 120 to 160 ° C, and more preferably 130 to 150 ° C.
また、本発明においては、本含浸工程におけるメラミン樹脂組成物のゲルタイムと紙間強化含浸工程におけるメラミン樹脂組成物のゲルタイムとの差が30秒以上であることが好ましく、45秒以上であることがより好ましい。即ち、以下の式を満たすことが好ましい。
本含浸工程におけるメラミン樹脂組成物のゲルタイム(秒)−紙間強化含浸工程におけるメラミン樹脂組成物のゲルタイム(秒)≧30(秒)
好ましくは以下の式を満たすことが好ましい。
本含浸工程におけるメラミン樹脂組成物のゲルタイム(秒)−紙間強化含浸工程におけるメラミン樹脂組成物のゲルタイム(秒)≧45(秒)
Further, in the present invention, the difference between the gel time of the melamine resin composition in the main impregnation step and the gel time of the melamine resin composition in the inter-paper reinforcing impregnation step is preferably 30 seconds or more, and preferably 45 seconds or more. More preferred. That is, it is preferable to satisfy the following formula.
Gel time (seconds) of melamine resin composition in this impregnation step-Gel time (seconds) of melamine resin composition in inter-paper reinforced impregnation step ≧ 30 (seconds)
It is preferable to satisfy the following formula.
Gel time (seconds) of melamine resin composition in this impregnation step-Gel time (seconds) of melamine resin composition in inter-paper strengthening impregnation step ≧ 45 (seconds)
本発明のプリプレグの樹脂付着量は特に限定されないが、53〜65重量%であればよく、55〜60重量%であることが好ましい。 Although the resin adhesion amount of the prepreg of the present invention is not particularly limited, it may be 53 to 65% by weight, and is preferably 55 to 60% by weight.
本発明のプリプレグには揮発分(溶剤)が残存していてもよく、5〜8重量%であればよく、5〜6.5重量%であることが好ましい。揮発分の残存により、プリプレグの取り扱いが容易になる。 Volatile matter (solvent) may remain in the prepreg of the present invention, and it may be 5 to 8% by weight, preferably 5 to 6.5% by weight. The remaining volatile matter facilitates handling of the prepreg.
化粧板
化粧板は、本発明のプリプレグと基材を基材に重ね合わせ、加熱下で圧力を加えて、樹脂を硬化させると共に化粧紙を基材に接着する化粧板となる。具体的には、本発明のプリプレグと基材を重ねて、プレス機で熱圧成型することによって作成される。なお、ここでいう化粧板には樹脂組成物の層を多重に積層したいわゆる積層化粧板も含まれる。
The decorative board is a decorative board in which the prepreg of the present invention and a base material are superposed on a base material, and pressure is applied under heating to cure the resin and bond the decorative paper to the base material. Specifically, the prepreg of the present invention and the substrate are overlapped and formed by hot pressing with a press. The decorative board here includes a so-called laminated decorative board in which multiple layers of the resin composition are laminated.
基材としては、パーチクルボード、MDF(中密度繊維板)、ケナフボード、ベニヤ合板などの木質系基材、アルミニウム板、ステンレス板などの金属板系基材、更には内装用材料及び外装用材料として用いられる、酸化マグネシウム、水酸化アルミニウム、酸化アルミニウム、酸化ケイ素、酸化チタン、塩化マグネシウム、珪酸カルシウム、火山性ガラス質材料、石膏(硫酸カルシウム)、石灰石(炭酸カルシウム)、水硬性セメントおよび気硬性セメントの群から選択される少なくとも1種の材料を硬化させた無機質系基材を例示することができる。 As base materials, particle board, MDF (medium density fiberboard), kenaf board, wood base material such as veneer plywood, metal plate base material such as aluminum plate, stainless steel plate, and further, interior materials and exterior materials Magnesium oxide, aluminum hydroxide, aluminum oxide, silicon oxide, titanium oxide, magnesium chloride, calcium silicate, volcanic glassy material, gypsum (calcium sulfate), limestone (calcium carbonate), hydraulic cement and pneumatic cement used An inorganic base material obtained by curing at least one material selected from the group can be exemplified.
成型は通常のショートサイクルメラミンと同様、冷却なしのHOT−HOTプレス法にて行われる。成型圧力は10〜30kg/cm2であることが好ましく、12〜20kg/cm2であることがより好ましい。成型温度は130〜250℃であることが好ましく、140〜220℃であることがより好ましい。成型時間は10秒〜30分であることが好ましく、30秒〜15分であることがより好ましい。 The molding is performed by the HOT-HOT press method without cooling as in the case of ordinary short cycle melamine. Preferably molding pressure is 10 to 30 kg / cm 2, more preferably 12~20kg / cm 2. The molding temperature is preferably 130 to 250 ° C, and more preferably 140 to 220 ° C. The molding time is preferably 10 seconds to 30 minutes, and more preferably 30 seconds to 15 minutes.
本発明の化粧板の光沢性はJIS Z 8741に規定されている方法で測定した20度グロス値が100以上であることが好ましく、110以上であることがより好ましい。 As for the glossiness of the decorative board of the present invention, the 20-degree gloss value measured by the method defined in JIS Z 8741 is preferably 100 or more, and more preferably 110 or more.
次に実施例、比較例によって本発明を詳細に説明する。ここで、実施例、比較例の「部」は重量部を示す。また、各実施例・比較例において具体的記載のない構成成分については実施例1記載の成分と同一品を使用した。
以下、各試験項目について説明する。
Next, the present invention will be described in detail by way of examples and comparative examples. Here, “parts” in Examples and Comparative Examples represent parts by weight. In addition, the same components as those described in Example 1 were used for the components not specifically described in each Example and Comparative Example.
Hereinafter, each test item will be described.
ゲルタイム:メラミン樹脂組成物のゲルタイムは、5mlのメラミン樹脂組成物を直径16.5mm、長さ165mmのガラス製試験管にサンプリングし、その表面が容量約3Lの沸騰水の液面下約3cmになるように固定し、樹脂液が透明から白濁するまでの時間(秒)を測定する。この測定は2回以上行い、その平均値をゲルタイムとした。 Gel time: The gel time of the melamine resin composition is that 5 ml of the melamine resin composition is sampled into a glass test tube having a diameter of 16.5 mm and a length of 165 mm, and the surface thereof is about 3 cm below the surface of boiling water having a capacity of about 3 L. And measure the time (seconds) until the resin liquid turns from transparent to cloudy. This measurement was performed twice or more, and the average value was taken as the gel time.
クラック:化粧板表面にクラックが発生するかどうかを目視で観察した。クラックないものを○、小さなマイクロクラックでも発生した場合は×と評価した。 Cracks: Whether or not cracks occurred on the decorative plate surface was visually observed. A case where no crack was observed was evaluated as “◯”, and a case where even a small micro crack was generated was evaluated as “×”.
光沢性:光沢度計 micro−TRI−gloss(Gardner社製品)を用いて、JIS Z 8741に規定されている方法に従って測定した。ここで、20度グロス値が100以上を○、80以上で100未満を△、80未満を×と評価した。 Glossiness: Glossiness Measured according to a method defined in JIS Z 8741 using a micro-TRI-gloss (Gardner product). Here, the 20 degree gloss value was evaluated as ◯ for 100 or more, Δ for 80 or more and Δ for less than 100, and × for less than 80.
鮮映性:携帯用鮮明度光沢度計PGD−IV(PGD計、財団法人日本色彩研究所、東京光電株式会社製)を用いて、その表示する鮮映性測定値(GD値)を測定した。GD値が0.4以上を○、0.3以上で0.4未満を△、0.3未満を×と評価した。 Sharpness: Using a portable sharpness / glossiness meter PGD-IV (PGD meter, Nippon Color Research Laboratories, manufactured by Tokyo Koden Co., Ltd.), the sharpness measurement value (GD value) to be displayed was measured. . A GD value of 0.4 or more was evaluated as ◯, 0.3 or more and less than 0.4 was evaluated as Δ, and less than 0.3 was evaluated as ×.
平滑性:蛍光灯から1メートル離した位置に化粧板を置き、表面に映る蛍光灯の直線部分の変形の状態を目視により観察することにより評価した。評価は、表面に映る蛍光灯の直線部分が良好な直線を維持している場合は○、波状が強い場合は△、そして、あばた強く境界線が不鮮明な場合は×とした。 Smoothness: Evaluation was made by placing a decorative plate at a position 1 meter away from the fluorescent lamp and visually observing the deformation state of the linear portion of the fluorescent lamp reflected on the surface. The evaluation was ○ when the straight line portion of the fluorescent lamp reflected on the surface maintained a good straight line, Δ when the wavy shape was strong, and × when the boundary line was sharp and the boundary line was not clear.
鉛筆硬度試験:JIS K 5600に規定されている方法による鉛筆引っかき値に準じて測定した。 Pencil hardness test: Measured according to the pencil scratch value according to the method defined in JIS K 5600.
引掻き硬度:JIS B試験(ダイヤモンド針、200g荷重)に規定されている方法に従い傷を付け、傷の深さを表面粗さ計にて測定した。傷の深さの3点平均が4ミクロン以下を○、それを超えるものは×と評価した。 Scratch hardness: A scratch was made according to the method specified in the JIS B test (diamond needle, 200 g load), and the depth of the scratch was measured with a surface roughness meter. A three-point average depth of scratches of 4 microns or less was evaluated as ◯, and a scratch depth exceeding that was evaluated as ×.
耐汚染性:JIS K6902に規定されている方法に従って測定した。 Contamination resistance: Measured according to the method defined in JIS K6902.
密着性:JAS2類浸漬試験に従い、70℃温水に2時間浸し、60℃オーブンにて3時間乾燥後に基材との層間剥離が全くないものを○、僅かでも剥離が生じた場合は×と評価した。 Adhesion: according to JAS2 immersion test, soaked in 70 ° C warm water for 2 hours, dried in a 60 ° C oven for 3 hours, evaluated as “O” when there was no delamination from the substrate, and evaluated as x when slight peeling occurred. did.
樹脂組成物A
水溶性メチロールメラミン樹脂(ニカレジンS−260、日本カーバイト株式会社製)を40℃温水に溶解し、固形分濃度56重量%とする。イミドジスルホン酸ジアンモニウム触媒(キャタニット、MRCユニテック株式会社製)の20重量%水溶液を上記樹脂液固形分500gに対して6g(樹脂液固形分100重量部に対して、1.2重量部)、レベリング剤(ノブコウェット50、サンノプコ株式会社製)を1g(樹脂液固形分100重量部に対して、0.2重量部)、消泡剤(BYK−093の1重量%希釈液 BYK製)を0.5g(樹脂液固形分100重量部に対して、0.1重量部)配合し、樹脂組成物Aを調整した。樹脂組成物Aのゲルタイムは120秒であった。
Resin composition A
A water-soluble methylol melamine resin (Nikaresin S-260, manufactured by Nippon Carbide Co., Ltd.) is dissolved in 40 ° C. warm water to give a solid content concentration of 56% by weight. 6 g of 20 wt% aqueous solution of diammonium imide disulfonate catalyst (Catanit, manufactured by MRC Unitech Co., Ltd.) with respect to 500 g of the resin liquid solids (1.2 parts by weight with respect to 100 parts by weight of resin liquid solids) , 1 g of a leveling agent (Nobco Wet 50, manufactured by San Nopco Co., Ltd.) (0.2 parts by weight with respect to 100 parts by weight of the resin liquid solid content), an antifoaming agent (1% by weight diluted solution of BYK-093 manufactured by BYK) 0.5 g (0.1 part by weight with respect to 100 parts by weight of the resin liquid solid content) was blended to prepare Resin Composition A. The gel time of the resin composition A was 120 seconds.
樹脂組成物B
水溶性メチロールメラミン樹脂(ニカレジンS−260、日本カーバイト株式会社製)を40℃温水に溶解し、固形分濃度56重量%とする。2−アミノ−2−メチル−1−プロパノール触媒(キャタニットA、MRCユニテック株式会社製)の50重量%水溶液を上記樹脂液固形分500gに対して3g(樹脂液固形分100重量部に対して、0.6重量部)、レベリング剤(ノブコウェット50、サンノプコ株式会社製)を1g(樹脂液固形分100重量部に対して、0.2重量部)、消泡剤(BYK−093の1重量%希釈液 BYK製)を0.5g(樹脂液固形分100重量部に対して、0.1重量部)配合し、樹脂組成物Bを調整した。樹脂組成物Bのゲルタイムは250秒であった。
Resin composition B
A water-soluble methylol melamine resin (Nikaresin S-260, manufactured by Nippon Carbide Co., Ltd.) is dissolved in 40 ° C. warm water to give a solid content concentration of 56% by weight. 3 g of a 50 wt% aqueous solution of 2-amino-2-methyl-1-propanol catalyst (Catanit A, manufactured by MRC Unitech Co., Ltd.) with respect to 500 g of the resin liquid solid content (based on 100 parts by weight of resin liquid solid content) 0.6 parts by weight), 1 g of a leveling agent (Nobco Wet 50, manufactured by San Nopco Co., Ltd.) (0.2 parts by weight with respect to 100 parts by weight of resin liquid solids), an antifoaming agent (1 of BYK-093) A resin composition B was prepared by blending 0.5 g of a weight% diluted solution (by BYK) (0.1 part by weight with respect to 100 parts by weight of the solid content of the resin liquid). The gel time of the resin composition B was 250 seconds.
樹脂組成物C
水溶性メチロールメラミン樹脂(ニカレジンS−260、日本カーバイト株式会社製)とメチルグリコシド樹脂(MEGA−6、群栄化学株式会社)を90:10の割合で、40℃温水に溶解し、固形分濃度56重量%とする。イミドジスルホン酸ジアンモニウム触媒(キャタニット、MRCユニテック株式会社製)の20重量%水溶液を上記樹脂液固形分500gに対して6g(樹脂液固形分100重量部に対して、1.2重量部)、レベリング剤(ノブコウェット50、サンノプコ株式会社製)を1g(樹脂液固形分100重量部に対して、0.2重量部)、消泡剤(BYK−093の1重量%希釈液 BYK製)を0.5g(樹脂液固形分100重量部に対して、0.1重量部)配合し、樹脂組成物Cを調整した。樹脂組成物Cのゲルタイムは150秒であった。
Resin composition C
A water-soluble methylol melamine resin (Nikaresin S-260, manufactured by Nippon Carbide Co., Ltd.) and a methyl glycoside resin (MEGA-6, Gunei Chemical Co., Ltd.) are dissolved at a ratio of 90:10 in hot water at 40 ° C. to obtain a solid content. The concentration is 56% by weight. 6 g of 20 wt% aqueous solution of diammonium imide disulfonate catalyst (Catanit, manufactured by MRC Unitech Co., Ltd.) with respect to 500 g of the resin liquid solids (1.2 parts by weight with respect to 100 parts by weight of resin liquid solids) , 1 g of a leveling agent (Nobco Wet 50, manufactured by San Nopco Co., Ltd.) (0.2 parts by weight with respect to 100 parts by weight of the resin liquid solid content), an antifoaming agent (1% by weight diluted solution of BYK-093 manufactured by BYK) 0.5 g (0.1 part by weight with respect to 100 parts by weight of the resin liquid solid content) was blended to prepare Resin Composition C. The gel time of the resin composition C was 150 seconds.
樹脂組成物D
水溶性メチロールメラミン樹脂(ニカレジンS−176、日本カーバイト株式会社製)とメチルグリコシド樹脂(MEGA−6、群栄化学株式会社)を90:10の割合で、40℃温水に溶解し、固形分濃度56重量%とする。2−アミノ−2−メチル−1−プロパノール触媒(キャタニットA、MRCユニテック株式会社製)の50重量%水溶液を上記樹脂液固形分500gに対して3g(樹脂液固形分100重量部に対して、0.6重量部)、レベリング剤(ノブコウェット50、サンノプコ株式会社製)を1g(樹脂液固形分100重量部に対して、0.2重量部)、消泡剤(BYK−093の1重量%希釈液 BYK製)を0.5g(樹脂液固形分100重量部に対して、0.1重量部)、KCフロック(W−100GK、日本製紙株式会社製)を5g(樹脂液固形分100重量部に対して、1重量部)配合し、樹脂組成物Dを調整した。樹脂組成物Dのゲルタイムは260秒であった。
Resin composition D
A water-soluble methylol melamine resin (Nikaresin S-176, manufactured by Nippon Carbide Co., Ltd.) and a methyl glycoside resin (MEGA-6, Gunei Chemical Co., Ltd.) are dissolved at a ratio of 90:10 in 40 ° C. hot water to obtain a solid content. The concentration is 56% by weight. 3 g of a 50 wt% aqueous solution of 2-amino-2-methyl-1-propanol catalyst (Catanit A, manufactured by MRC Unitech Co., Ltd.) with respect to 500 g of the resin liquid solid content (based on 100 parts by weight of resin liquid solid content) 0.6 parts by weight), 1 g of a leveling agent (Nobco Wet 50, manufactured by San Nopco Co., Ltd.) (0.2 parts by weight with respect to 100 parts by weight of resin liquid solids), an antifoaming agent (1 of BYK-093) 0.5% by weight (diluted solution BYK) (0.1 parts by weight with respect to 100 parts by weight of resin liquid solids) and 5 g of KC Flock (W-100GK, manufactured by Nippon Paper Industries Co., Ltd.) The resin composition D was prepared by blending 1 part by weight with respect to 100 parts by weight. The gel time of the resin composition D was 260 seconds.
樹脂組成物E
水溶性メチロールメラミン樹脂(ニカレジンS−260、日本カーバイト株式会社製)とメチルグリコシド樹脂(MEGA−6、群栄化学株式会社)を90:10の割合で、40℃温水に溶解し、固形分濃度56重量%とする。イミドジスルホン酸ジアンモニウム触媒(キャタニット、MRCユニテック株式会社製)の20重量%水溶液を上記樹脂液固形分500gに対して7.5g(樹脂液固形分100重量部に対して、1.5重量部)、レベリング剤(ノブコウェット50、サンノプコ株式会社製)を1g(樹脂液固形分100重量部に対して、0.2重量部)、消泡剤(BYK−093の1重量%希釈液 BYK製)を0.5g(樹脂液固形分100重量部に対して、0.1重量部)配合し、樹脂組成物Eを調整した。樹脂組成物Eのゲルタイムは195秒であった。
Resin composition E
A water-soluble methylol melamine resin (Nikaresin S-260, manufactured by Nippon Carbide Co., Ltd.) and a methyl glycoside resin (MEGA-6, Gunei Chemical Co., Ltd.) are dissolved at a ratio of 90:10 in hot water at 40 ° C. to obtain a solid content. The concentration is 56% by weight. 7.5 g of a 20% by weight aqueous solution of diammonium imidodisulfonate catalyst (Catanit, manufactured by MRC Unitech Co., Ltd.) with respect to 500 g of the resin liquid solid content (1.5 weight with respect to 100 parts by weight of resin liquid solid content) Part), leveling agent (Nobco Wet 50, manufactured by San Nopco Co., Ltd.) 1 g (0.2 part by weight with respect to 100 parts by weight of resin liquid solid content), antifoaming agent (1% by weight diluted solution of BYK-093 BYK 0.5 g (0.1 part by weight with respect to 100 parts by weight of the resin liquid solid content) was blended to prepare Resin Composition E. The gel time of the resin composition E was 195 seconds.
樹脂組成物F
水溶性メチロールメラミン樹脂(ニカレジンS−260、日本カーバイト株式会社製)とメチルグリコシド樹脂(MEGA−6、群栄化学株式会社)を80:20の割合で、40℃温水に溶解し、固形分濃度56重量%とする。イミドジスルホン酸ジアンモニウム触媒(キャタニット、MRCユニテック株式会社製)の20重量%水溶液を上記樹脂液固形分500gに対して6g(樹脂液固形分100重量部に対して、1.2重量部)、レベリング剤(ノブコウェット50、サンノプコ株式会社製)を1g(樹脂液固形分100重量部に対して、0.2重量部)、消泡剤(BYK−093の1重量%希釈液 BYK製)を0.5g(樹脂液固形分100重量部に対して、0.1重量部)配合し、樹脂組成物Fを調整した。樹脂組成物Fのゲルタイムは100秒であった。
Resin composition F
A water-soluble methylol melamine resin (Nikaresin S-260, manufactured by Nippon Carbide Co., Ltd.) and a methyl glycoside resin (MEGA-6, Gunei Chemical Co., Ltd.) are dissolved in warm water at 40 ° C. at a ratio of 80:20 to obtain a solid content. The concentration is 56% by weight. 6 g of 20 wt% aqueous solution of diammonium imide disulfonate catalyst (Catanit, manufactured by MRC Unitech Co., Ltd.) with respect to 500 g of the resin liquid solids (1.2 parts by weight with respect to 100 parts by weight of resin liquid solids) , 1 g of a leveling agent (Nobco Wet 50, manufactured by San Nopco Co., Ltd.) (0.2 parts by weight with respect to 100 parts by weight of the resin liquid solid content), an antifoaming agent (1% by weight diluted solution of BYK-093 manufactured by BYK) 0.5 g (0.1 part by weight with respect to 100 parts by weight of the resin liquid solid content) was blended to prepare Resin Composition F. The gel time of the resin composition F was 100 seconds.
樹脂組成物G
水溶性メチロールメラミン樹脂(ニカレジンS−260、日本カーバイト株式会社製)とメチルグリコシド樹脂(MEGA−6、群栄化学株式会社)を70:30の割合で、40℃温水に溶解し、固形分濃度56重量%とする。イミドジスルホン酸ジアンモニウム触媒(キャタニット、MRCユニテック株式会社製)の20重量%水溶液を上記樹脂液固形分500gに対して6g(樹脂液固形分100重量部に対して、1.2重量部)、レベリング剤(ノブコウェット50、サンノプコ株式会社製)を1g(樹脂液固形分100重量部に対して、0.2重量部)、消泡剤(BYK−093の1重量%希釈液 BYK製)を0.5g(樹脂液固形分100重量部に対して、0.1重量部)、KCフロック(W−100GK、日本製紙株式会社製)を5g(樹脂液固形分100重量部に対して、1重量部)を配合し、樹脂組成物Gを調整した。樹脂組成物Gのゲルタイムは280秒であった。
Resin composition G
A water-soluble methylol melamine resin (Nikaresin S-260, manufactured by Nippon Carbide Co., Ltd.) and a methyl glycoside resin (MEGA-6, Gunei Chemical Co., Ltd.) are dissolved in 40 ° C. hot water at a ratio of 70:30 to obtain a solid content. The concentration is 56% by weight. 6 g of 20 wt% aqueous solution of diammonium imide disulfonate catalyst (Catanit, manufactured by MRC Unitech Co., Ltd.) with respect to 500 g of the resin liquid solids (1.2 parts by weight with respect to 100 parts by weight of resin liquid solids) , 1 g of a leveling agent (Nobco Wet 50, manufactured by San Nopco Co., Ltd.) (0.2 parts by weight with respect to 100 parts by weight of the resin liquid solid content), an antifoaming agent (1% by weight diluted solution of BYK-093 manufactured by BYK) 0.5 g (0.1 parts by weight with respect to 100 parts by weight of resin liquid solids), 5 g of KC floc (W-100GK, manufactured by Nippon Paper Industries Co., Ltd.) with respect to 100 parts by weight of resin liquid solids, 1 part by weight) was blended to prepare a resin composition G. The gel time of the resin composition G was 280 seconds.
樹脂組成物H
水溶性メチロールメラミン樹脂(ニカレジンS−260、日本カーバイト株式会社製)とブチルグリコシド樹脂(群栄化学株式会社)を70:30の割合で、40℃温水に溶解し、固形分濃度56重量%とする。イミドジスルホン酸ジアンモニウム触媒(キャタニット、MRCユニテック株式会社製)の20重量%水溶液を上記樹脂液固形分500gに対して6g(樹脂液固形分100重量部に対して、1.2重量部)、レベリング剤(ノブコウェット50、サンノプコ株式会社製)を1g(樹脂液固形分100重量部に対して、0.2重量部)、消泡剤(BYK−093の1重量%希釈液 BYK製)を0.5g(樹脂液固形分100重量部に対して、0.1重量部)配合し、樹脂組成物Hを調整した。樹脂組成物Hのゲルタイムは105秒であった。
Resin composition H
A water-soluble methylol melamine resin (Nical Resin S-260, manufactured by Nippon Carbide Co., Ltd.) and a butyl glycoside resin (Gunei Chemical Co., Ltd.) are dissolved in 40: 30 ° C. warm water at a ratio of 70:30, and the solid content concentration is 56% by weight. And 6 g of 20 wt% aqueous solution of diammonium imide disulfonate catalyst (Catanit, manufactured by MRC Unitech Co., Ltd.) with respect to 500 g of the resin liquid solids (1.2 parts by weight with respect to 100 parts by weight of resin liquid solids) , 1 g of a leveling agent (Nobco Wet 50, manufactured by San Nopco Co., Ltd.) (0.2 parts by weight with respect to 100 parts by weight of the resin liquid solid content), an antifoaming agent (1% by weight diluted solution of BYK-093 manufactured by BYK) 0.5 g (0.1 part by weight with respect to 100 parts by weight of the resin liquid solid content) was blended to prepare Resin Composition H. The gel time of the resin composition H was 105 seconds.
樹脂組成物I
水溶性メチロールメラミン樹脂(ニカレジンS−260、日本カーバイト株式会社製)を40℃温水に溶解し、固形分濃度56重量%とする。塩化アンモニウム触媒(和光純薬株式会社製)の50重量%水溶液を上記樹脂液固形分500gに対して8g(樹脂液固形分100重量部に対して、1.6重量部)、レベリング剤(ノブコウェット50、サンノプコ株式会社製)を1g(樹脂液固形分100重量部に対して、0.2重量部)、消泡剤(BYK−093の1重量%希釈液 BYK製)を0.5g(樹脂液固形分100重量部に対して、0.1重量部)配合し、樹脂組成物Iを調整した。樹脂組成物Iのゲルタイムは150秒であった。
Resin composition I
A water-soluble methylol melamine resin (Nikaresin S-260, manufactured by Nippon Carbide Co., Ltd.) is dissolved in 40 ° C. warm water to give a solid content concentration of 56% by weight. A 50% aqueous solution of ammonium chloride catalyst (manufactured by Wako Pure Chemical Industries, Ltd.) is 8 g (1.6 parts by weight with respect to 100 parts by weight of resin liquid solids) with respect to 500 g of the resin liquid solids, and a leveling agent (Nobco). 1 g of wet 50 (manufactured by San Nopco Co., Ltd.) (0.2 parts by weight with respect to 100 parts by weight of resin liquid solid content), 0.5 g of antifoaming agent (1% by weight diluted solution of BYK-093 manufactured by BYK) The resin composition I was prepared by blending 0.1 parts by weight with respect to 100 parts by weight of the resin liquid solid content. The gel time of the resin composition I was 150 seconds.
樹脂組成物J
水溶性メチロールメラミン樹脂(ニカレジンS−260、日本カーバイト株式会社製)とメチルグリコシド樹脂(MEGA−6、群栄化学株式会社)を80:20の割合で40℃温水に溶解し、固形分濃度56重量%とする。p−トルエンスルホン酸触媒(和光純薬株式会社製)の50重量%水溶液を上記樹脂液固形分500gに対して4g(樹脂液固形分100重量部に対して、0.8重量部)、レべリング剤(ノブコウェット50、サンノプコ株式会社製)を1g(樹脂液固形分100重量部に対して、0.2重量部)、消泡剤(BYK−093の1重量%希釈液 BYK製)を0.5g(樹脂液固形分100重量部に対して、0.1重量部)配合し、樹脂組成物Jを調整した。樹脂組成物Jのゲルタイムは140秒であった。
Resin composition J
A water-soluble methylol melamine resin (Nikaresin S-260, manufactured by Nippon Carbide Co., Ltd.) and a methyl glycoside resin (MEGA-6, Gunei Chemical Co., Ltd.) are dissolved in warm water at 40 ° C. at a ratio of 80:20 to obtain a solid content concentration. 56% by weight. 4 g of a 50 wt% aqueous solution of p-toluenesulfonic acid catalyst (manufactured by Wako Pure Chemical Industries, Ltd.) with respect to 500 g of the resin liquid solids (0.8 parts by weight with respect to 100 parts by weight of resin liquid solids) 1 g of a belling agent (Nobco Wet 50, manufactured by San Nopco Co., Ltd.) (0.2 parts by weight with respect to 100 parts by weight of the resin liquid solid content), an antifoaming agent (a 1% by weight diluted solution of BYK-093 manufactured by BYK) 0.5 g (0.1 part by weight with respect to 100 parts by weight of the resin liquid solid content) was blended to prepare Resin Composition J. The gel time of the resin composition J was 140 seconds.
樹脂組成物K
水溶性メチロールメラミン樹脂(ニカレジンS−260、日本カーバイト株式会社製)とメチルグリコシド樹脂(MEGA−6、群栄化学株式会社)を70:30の割合で40℃温水に溶解し、固形分濃度56重量%とする。p−トルエンスルホン酸アンモニウム触媒(和光純薬株式会社製)の50重量%水溶液を上記樹脂液固形分500gに対して4g(樹脂液固形分100重量部に対して、0.8重量部)、レべリング剤(ノブコウェット50、サンノプコ株式会社製)を1g(樹脂液固形分100重量部に対して、0.2重量部)、消泡剤(BYK−093の1重量%希釈液 BYK製)を0.5g(樹脂液固形分100重量部に対して、0.1重量部)配合し樹脂組成物溶液Kを調整した。本樹脂液のゲルタイムは160秒であった。
Resin composition K
A water-soluble methylol melamine resin (Nikaresin S-260, manufactured by Nippon Carbide Co., Ltd.) and a methyl glycoside resin (MEGA-6, Gunei Chemical Co., Ltd.) are dissolved in 40 ° C. hot water at a ratio of 70:30 to obtain a solid content concentration. 56% by weight. 4 g of a 50 wt% aqueous solution of ammonium p-toluenesulfonate catalyst (manufactured by Wako Pure Chemical Industries, Ltd.) with respect to 500 g of the resin liquid solids (0.8 parts by weight with respect to 100 parts by weight of the resin liquid solids), 1 g of leveling agent (Nobuco Wet 50, manufactured by San Nopco Co., Ltd.) (0.2 parts by weight with respect to 100 parts by weight of resin liquid solid content), antifoaming agent (1% by weight diluted solution of BYK-093, manufactured by BYK) 0.5 g (0.1 part by weight with respect to 100 parts by weight of the resin liquid solid content) was added to prepare a resin composition solution K. The gel time of this resin liquid was 160 seconds.
実施例1
80g/m2のチタン紙を樹脂組成物Aに含浸した(紙間強化含浸)後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Bに含浸し(本含浸)、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ15mmのパーチクルボード(大倉工業株式会社製)に載せ、150℃、12kg/cm2、7分の熱圧成型で化粧板を得た。得られた化粧板の物性を表2に記載する。
Example 1
After impregnating 80 g / m 2 of titanium paper into the resin composition A (strengthening inter-paper impregnation), drying in a hot air circulating oven at 135 ° C. for 1 minute, and then impregnating into the resin composition B (main impregnation), It was dried at 135 ° C. for 3 minutes to obtain a prepreg having a resin adhesion amount (RC) of 58 wt%. This was placed on a 15 mm thick particle board (manufactured by Okura Kogyo Co., Ltd.), and a decorative board was obtained by hot-pressure molding at 150 ° C., 12 kg / cm 2 for 7 minutes. Table 2 shows the physical properties of the decorative board obtained.
実施例2
80g/m2のチタン紙を樹脂組成物Cに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Bに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ15mmのパーチクルボード(大倉工業株式会社製)に載せ、150℃、12kg/cm2、7分の熱圧成型で化粧板を得た。得られた化粧板の物性を表2に記載する。
Example 2
After impregnating resin composition C with 80 g / m 2 of titanium paper, it was dried in a hot air circulating oven at 135 ° C. for 1 minute, then impregnated into resin composition B, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 58% by weight was obtained. This was placed on a 15 mm thick particle board (manufactured by Okura Kogyo Co., Ltd.), and a decorative board was obtained by hot-pressure molding at 150 ° C., 12 kg / cm 2 for 7 minutes. Table 2 shows the physical properties of the decorative board obtained.
実施例3
80g/m2のチタン紙を樹脂組成物Eに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Dに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ15mmのパーチクルボード(大倉工業株式会社製)に載せ、150℃、12kg/cm2、7分の熱圧成型で化粧板を得た。得られた化粧板の物性を表2に記載する。
Example 3
After impregnating resin composition E with 80 g / m 2 of titanium paper, it was dried in a hot air circulating oven at 135 ° C. for 1 minute, then impregnated into resin composition D, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 58% by weight was obtained. This was placed on a 15 mm thick particle board (manufactured by Okura Kogyo Co., Ltd.), and a decorative board was obtained by hot-pressure molding at 150 ° C., 12 kg / cm 2 for 7 minutes. Table 2 shows the physical properties of the decorative board obtained.
実施例4
80g/m2のチタン紙を樹脂組成物Iに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Dに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ15mmのパーチクルボード(大倉工業株式会社製)に載せ、150℃、12kg/cm2、7分の熱圧成型で化粧板を得た。得られた化粧板の物性を表2に記載する。
Example 4
After impregnating resin composition I with 80 g / m 2 of titanium paper, it was dried in a 135 ° C. hot air circulating oven for 1 minute, then impregnated into resin composition D, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 58% by weight was obtained. This was placed on a 15 mm thick particle board (manufactured by Okura Kogyo Co., Ltd.), and a decorative board was obtained by hot-pressure molding at 150 ° C., 12 kg / cm 2 for 7 minutes. Table 2 shows the physical properties of the decorative board obtained.
実施例5
80g/m2のチタン紙を樹脂組成物Iに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Eに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ15mmのパーチクルボード(大倉工業株式会社製)に載せ、150℃、12kg/cm2、7分の熱圧成型で化粧板を得た。得られた化粧板の物性を表2に記載する。
Example 5
After impregnating resin composition I with 80 g / m 2 of titanium paper, it was dried in a 135 ° C. hot air circulating oven for 1 minute, then impregnated in resin composition E, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 58% by weight was obtained. This was placed on a 15 mm thick particle board (manufactured by Okura Kogyo Co., Ltd.), and a decorative board was obtained by hot-pressure molding at 150 ° C., 12 kg / cm 2 for 7 minutes. Table 2 shows the physical properties of the decorative board obtained.
実施例6
100g/m2のチタン紙を樹脂組成物Jに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Gに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ18mmのパーチクルボード(大倉工業株式会社製)に載せ、150℃、12kg/cm2、7分の熱圧成型で化粧板を得た。得られた化粧板の物性を表2に記載する。
Example 6
After impregnating resin composition J with 100 g / m 2 of titanium paper, it was dried in a 135 ° C. hot air circulating oven for 1 minute, then impregnated into resin composition G, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 58% by weight was obtained. This was placed on a 18 mm thick particle board (manufactured by Okura Kogyo Co., Ltd.), and a decorative board was obtained by hot-pressure molding at 150 ° C., 12 kg / cm 2 for 7 minutes. Table 2 shows the physical properties of the decorative board obtained.
実施例7
100g/m2のチタン紙を樹脂組成物Kに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Bに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が59重量%のプリプレグを得た。これを厚さ18mmのパーチクルボード(大倉工業株式会社製)に載せ、150℃、12kg/cm2、7分の熱圧成型で化粧板を得た。得られた化粧板の物性を表2に記載する。
Example 7
After impregnating resin composition K with 100 g / m 2 of titanium paper, it was dried in a 135 ° C. hot air circulating oven for 1 minute, then impregnated into resin composition B, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 59% by weight was obtained. This was placed on a 18 mm thick particle board (manufactured by Okura Kogyo Co., Ltd.), and a decorative board was obtained by hot-pressure molding at 150 ° C., 12 kg / cm 2 for 7 minutes. Table 2 shows the physical properties of the decorative board obtained.
比較例1
80g/m2のチタン紙を樹脂組成物Bに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Aに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ15mmのパーチクルボード(大倉工業株式会社製)に載せ、150℃、12kg/cm2、7分の熱圧成型で化粧板を得た。得られた化粧板の物性を表2に記載する。
Comparative Example 1
After impregnating resin composition B with 80 g / m 2 of titanium paper, it was dried in a 135 ° C. hot air circulating oven for 1 minute, then impregnated into resin composition A, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 58% by weight was obtained. This was placed on a 15 mm thick particle board (manufactured by Okura Kogyo Co., Ltd.), and a decorative board was obtained by hot-pressure molding at 150 ° C., 12 kg / cm 2 for 7 minutes. Table 2 shows the physical properties of the decorative board obtained.
比較例2
80g/m2のチタン紙を樹脂組成物Dに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Cに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ15mmのパーチクルボード(大倉工業株式会社製)に載せ、150℃、12kg/cm2、7分の熱圧成型で化粧板を得た。得られた化粧板の物性を表2に記載する。
Comparative Example 2
After impregnating resin composition D with 80 g / m 2 of titanium paper, it was dried in a 135 ° C. hot-air circulating oven for 1 minute, then impregnated into resin composition C, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 58% by weight was obtained. This was placed on a 15 mm thick particle board (manufactured by Okura Kogyo Co., Ltd.), and a decorative board was obtained by hot-pressure molding at 150 ° C., 12 kg / cm 2 for 7 minutes. Table 2 shows the physical properties of the decorative board obtained.
比較例3
80g/m2のチタン紙を樹脂組成物Fに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Eに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ18mmのパーチクルボード(大倉工業株式会社製)に載せ、150℃、12kg/cm2、7分の熱圧成型で化粧板を得た。得られた化粧板の物性を表2に記載する。
Comparative Example 3
After impregnating resin composition F with 80 g / m 2 of titanium paper, it was dried in a hot air circulating oven at 135 ° C. for 1 minute, then impregnated into resin composition E, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 58% by weight was obtained. This was placed on a 18 mm thick particle board (manufactured by Okura Kogyo Co., Ltd.), and a decorative board was obtained by hot-pressure molding at 150 ° C., 12 kg / cm 2 for 7 minutes. Table 2 shows the physical properties of the decorative board obtained.
比較例4
100g/m2のチタン紙を樹脂組成物Gに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Jに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ18mmのパーチクルボード(大倉工業株式会社製)に載せ、150℃、12kg/cm2、7分の熱圧成型で化粧板を得た。得られた化粧板の物性を表2に記載する。
Comparative Example 4
After impregnating resin composition G with 100 g / m 2 of titanium paper, it was dried in a 135 ° C. hot air circulating oven for 1 minute, then impregnated into resin composition J, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 58% by weight was obtained. This was placed on a 18 mm thick particle board (manufactured by Okura Kogyo Co., Ltd.), and a decorative board was obtained by hot-pressure molding at 150 ° C., 12 kg / cm 2 for 7 minutes. Table 2 shows the physical properties of the decorative board obtained.
比較例5
100g/m2のチタン紙を樹脂組成物Fに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Kに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が59重量%のプリプレグを得た。これを厚さ18mmのパーチクルボード(大倉工業株式会社製)に載せ、155℃、15kg/cm2、10分の熱圧成型で化粧板を得た。得られた化粧板の物性を表2に記載する。
Comparative Example 5
After impregnating resin composition F with 100 g / m 2 of titanium paper, it was dried in a 135 ° C. hot-air circulating oven for 1 minute, then impregnated into resin composition K, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 59% by weight was obtained. This was placed on a 18 mm thick particle board (manufactured by Okura Kogyo Co., Ltd.) to obtain a decorative board by hot pressing at 155 ° C., 15 kg / cm 2 for 10 minutes. Table 2 shows the physical properties of the decorative board obtained.
実施例8
80g/m2のチタン紙を樹脂組成物Aに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Bに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ6mmのMDF(大建工業株式会社製)に載せ、180℃、18kg/cm2、60秒の熱圧成型で化粧板を得た。得られた化粧板の物性を表3に記載する。
Example 8
After impregnating resin composition A with 80 g / m 2 of titanium paper, it was dried in a hot air circulating oven at 135 ° C. for 1 minute, then impregnated into resin composition B, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 58% by weight was obtained. This was placed on a 6 mm thick MDF (manufactured by Daiken Kogyo Co., Ltd.), and a decorative board was obtained by hot pressing at 180 ° C., 18 kg / cm 2 for 60 seconds. Table 3 shows the physical properties of the decorative sheet obtained.
実施例9
80g/m2のチタン紙を樹脂組成物Cに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Bに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ6mmのMDF(大建工業株式会社製)に載せ、180℃、18kg/cm2、60秒の熱圧成型で化粧板を得た。得られた化粧板の物性を表3に記載する。
Example 9
After impregnating resin composition C with 80 g / m 2 of titanium paper, it was dried in a hot air circulating oven at 135 ° C. for 1 minute, then impregnated into resin composition B, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 58% by weight was obtained. This was placed on a 6 mm thick MDF (manufactured by Daiken Kogyo Co., Ltd.), and a decorative board was obtained by hot pressing at 180 ° C., 18 kg / cm 2 for 60 seconds. Table 3 shows the physical properties of the decorative sheet obtained.
実施例10
80g/m2のチタン紙を樹脂組成物Eに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Dに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ6mmのMDF(大建工業株式会社製)に載せ、180℃、18kg/cm2、60秒の熱圧成型で化粧板を得た。得られた化粧板の物性を表3に記載する。
Example 10
After impregnating resin composition E with 80 g / m 2 of titanium paper, it was dried in a hot air circulating oven at 135 ° C. for 1 minute, then impregnated into resin composition D, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 58% by weight was obtained. This was placed on a 6 mm thick MDF (manufactured by Daiken Kogyo Co., Ltd.), and a decorative board was obtained by hot pressing at 180 ° C., 18 kg / cm 2 for 60 seconds. Table 3 shows the physical properties of the decorative sheet obtained.
実施例11
80g/m2のチタン紙を樹脂組成物Iに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Dに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ6mmのMDF(大建工業株式会社製)に載せ、180℃、18kg/cm2、60秒の熱圧成型で化粧板を得た。得られた化粧板の物性を表3に記載する。
Example 11
After impregnating resin composition I with 80 g / m 2 of titanium paper, it was dried in a 135 ° C. hot air circulating oven for 1 minute, then impregnated into resin composition D, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 58% by weight was obtained. This was placed on a 6 mm thick MDF (manufactured by Daiken Kogyo Co., Ltd.), and a decorative board was obtained by hot pressing at 180 ° C., 18 kg / cm 2 for 60 seconds. Table 3 shows the physical properties of the decorative sheet obtained.
実施例12
80g/m2のチタン紙を樹脂組成物Iに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Eに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ6mmのMDF(大建工業株式会社製)に載せ、180℃、18kg/cm2、60秒の熱圧成型で化粧板を得た。得られた化粧板の物性を表3に記載する。
Example 12
After impregnating resin composition I with 80 g / m 2 of titanium paper, it was dried in a 135 ° C. hot air circulating oven for 1 minute, then impregnated in resin composition E, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 58% by weight was obtained. This was placed on a 6 mm thick MDF (manufactured by Daiken Kogyo Co., Ltd.), and a decorative board was obtained by hot pressing at 180 ° C., 18 kg / cm 2 for 60 seconds. Table 3 shows the physical properties of the decorative sheet obtained.
実施例13
100g/m2のチタン紙を樹脂組成物Jに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Gに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ3mmのダイライト(大建工業株式会社製)に載せ、180℃、18kg/cm2、60秒の熱圧成型で化粧板を得た。得られた化粧板の物性を表3に記載する。
Example 13
After impregnating resin composition J with 100 g / m 2 of titanium paper, it was dried in a 135 ° C. hot air circulating oven for 1 minute, then impregnated into resin composition G, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 58% by weight was obtained. This was placed on a 3 mm thick die light (manufactured by Daiken Kogyo Co., Ltd.), and a decorative board was obtained by hot pressing at 180 ° C., 18 kg / cm 2 for 60 seconds. Table 3 shows the physical properties of the decorative sheet obtained.
実施例14
100g/m2のチタン紙を樹脂組成物Kに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Bに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が59重量%のプリプレグを得た。これを厚さ3mmのダイライト(大建工業株式会社製)に載せ、180℃、18kg/cm2、60秒の熱圧成型で化粧板を得た。得られた化粧板の物性を表3に記載する。
Example 14
After impregnating resin composition K with 100 g / m 2 of titanium paper, it was dried in a 135 ° C. hot air circulating oven for 1 minute, then impregnated into resin composition B, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 59% by weight was obtained. This was placed on a 3 mm thick die light (manufactured by Daiken Kogyo Co., Ltd.), and a decorative board was obtained by hot pressing at 180 ° C., 18 kg / cm 2 for 60 seconds. Table 3 shows the physical properties of the decorative sheet obtained.
比較例6
80g/m2のチタン紙を樹脂組成物Bに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Aに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ6mmのMDF(大建工業株式会社製)に載せ、180℃、18kg/cm2、60秒の熱圧成型で化粧板を得た。得られた化粧板の物性を表3に記載する。
Comparative Example 6
After impregnating resin composition B with 80 g / m 2 of titanium paper, it was dried in a 135 ° C. hot air circulating oven for 1 minute, then impregnated into resin composition A, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 58% by weight was obtained. This was placed on a 6 mm thick MDF (manufactured by Daiken Kogyo Co., Ltd.), and a decorative board was obtained by hot pressing at 180 ° C., 18 kg / cm 2 for 60 seconds. Table 3 shows the physical properties of the decorative sheet obtained.
比較例7
80g/m2のチタン紙を樹脂組成物Dに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Cに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ6mmのMDF(大建工業株式会社製)に載せ、180℃、18kg/cm2、60秒の熱圧成型で化粧板を得た。得られた化粧板の物性を表3に記載する。
Comparative Example 7
After impregnating resin composition D with 80 g / m 2 of titanium paper, it was dried in a 135 ° C. hot-air circulating oven for 1 minute, then impregnated into resin composition C, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 58% by weight was obtained. This was placed on a 6 mm thick MDF (manufactured by Daiken Kogyo Co., Ltd.), and a decorative board was obtained by hot pressing at 180 ° C., 18 kg / cm 2 for 60 seconds. Table 3 shows the physical properties of the decorative sheet obtained.
比較例8
80g/m2のチタン紙を樹脂組成物Fに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Eに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ6mmのMDF(大建工業株式会社製)に載せ、180℃、18kg/cm2、60秒の熱圧成型で化粧板を得た。得られた化粧板の物性を表3に記載する。
Comparative Example 8
After impregnating resin composition F with 80 g / m 2 of titanium paper, it was dried in a hot air circulating oven at 135 ° C. for 1 minute, then impregnated into resin composition E, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 58% by weight was obtained. This was placed on a 6 mm thick MDF (manufactured by Daiken Kogyo Co., Ltd.), and a decorative board was obtained by hot pressing at 180 ° C., 18 kg / cm 2 for 60 seconds. Table 3 shows the physical properties of the decorative sheet obtained.
比較例9
100g/m2のチタン紙を樹脂組成物Gに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Jに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が58重量%のプリプレグを得た。これを厚さ3mmのダイライト(大建工業株式会社製)に載せ、180℃、18kg/cm2、60秒の熱圧成型で化粧板を得た。得られた化粧板の物性を表3に記載する。
Comparative Example 9
After impregnating resin composition G with 100 g / m 2 of titanium paper, it was dried in a 135 ° C. hot air circulating oven for 1 minute, then impregnated into resin composition J, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 58% by weight was obtained. This was placed on a 3 mm thick die light (manufactured by Daiken Kogyo Co., Ltd.), and a decorative board was obtained by hot pressing at 180 ° C., 18 kg / cm 2 for 60 seconds. Table 3 shows the physical properties of the decorative sheet obtained.
比較例10
100g/m2のチタン紙を樹脂組成物Fに含浸した後、135℃熱風循環オーブンで一分間乾燥させた後、続けて樹脂組成物Kに含浸し、135℃で3分乾燥し、樹脂付着量(RC)が59重量%のプリプレグを得た。これを厚さ3mmのダイライト(大建工業株式会社製)に載せ、180℃、18kg/cm2、60秒の熱圧成型で化粧板を得た。得られた化粧板の物性を表3に記載する。
Comparative Example 10
After impregnating resin composition F with 100 g / m 2 of titanium paper, it was dried in a 135 ° C. hot-air circulating oven for 1 minute, then impregnated into resin composition K, and dried at 135 ° C. for 3 minutes to adhere the resin. A prepreg having an amount (RC) of 59% by weight was obtained. This was placed on a 3 mm thick die light (manufactured by Daiken Kogyo Co., Ltd.), and a decorative board was obtained by hot pressing at 180 ° C., 18 kg / cm 2 for 60 seconds. Table 3 shows the physical properties of the decorative sheet obtained.
実施例に用いた組成物配合を表1にまとめる。
実施例および比較例を表2、表3に示す。
実施例1〜14の化粧板は、JIS、JASに規定されている鉛筆硬度、引掻き硬度、耐汚染性、密着性の化粧板として必要な一般的な特性を有するとともに、良好な光沢性、鮮映性、平滑性を有していることが示された。
比較例1〜10の化粧板は、実施例1〜14の化粧板と比較して、明らかに光沢性、鮮映性、平滑性で劣っていることが示された。
The decorative boards of Examples 1 to 14 have general properties necessary for a decorative board having pencil hardness, scratch hardness, stain resistance, and adhesion as defined in JIS and JAS, as well as good gloss and freshness. It was shown that the film had good visual properties and smoothness.
It was shown that the decorative boards of Comparative Examples 1-10 were clearly inferior in glossiness, sharpness, and smoothness as compared with the decorative boards of Examples 1-14.
本発明の化粧板の製造法により、ショートサイクル法において製造された化粧板でも、高圧メラミン化粧板に匹敵する高い光沢と高い鮮映性、良好な平滑性を備えた化粧板の製造が可能になる。 The decorative board manufacturing method of the present invention makes it possible to manufacture a decorative board having high gloss, high definition and good smoothness comparable to a high-pressure melamine decorative board, even with a decorative board manufactured by the short cycle method. Become.
Claims (4)
ゲルタイムが120秒以上250秒以下であるメラミン樹脂組成物を、化粧紙に含浸する工程(紙間強化含浸工程)、及び
ゲルタイムが150秒を越えて400秒以下であるメラミン樹脂組成物を、紙間強化含浸工程を経た化粧紙に含浸する工程(本含浸工程)により、メラミン樹脂を化粧紙に含浸し、以下の式を満たすことを特徴とする化粧板の製造法。
本含浸工程のゲルタイム(秒)−紙間強化含浸工程のゲルタイム(秒)≧30(秒) In a method for producing a decorative board in which a prepreg obtained by impregnating and drying a melamine resin on a decorative paper is superimposed on a base material, pressure is applied under heating, the resin is cured and the decorative paper is adhered to the base material.
A step of impregnating a decorative paper with a melamine resin composition having a gel time of 120 seconds or more and 250 seconds or less (inter-paper reinforcing impregnation step); and a melamine resin composition having a gel time of more than 150 seconds and not more than 400 seconds, A method for producing a decorative board, wherein the decorative paper impregnated with melamine resin is impregnated by a step of impregnating the decorative paper that has undergone the intertempering impregnation step (this impregnation step), and the following formula is satisfied.
Gel time (seconds) of the main impregnation step-Gel time (seconds) of the inter-paper reinforced impregnation step ≧ 30 (seconds)
ゲルタイムが150秒を越えて400秒以下であるメラミン樹脂組成物を、紙間強化含浸工程を経た化粧紙に含浸する工程(本含浸工程)により、メラミン樹脂を化粧紙に含浸し、以下の式を満たすことを特徴とするプリプレグの製造法。
本含浸工程のゲルタイム(秒)−紙間強化含浸工程のゲルタイム(秒)≧30(秒) A step of impregnating a decorative paper with a melamine resin composition having a gel time of 120 seconds or more and 250 seconds or less (inter-paper reinforcing impregnation step); and a melamine resin composition having a gel time of more than 150 seconds and not more than 400 seconds, A method for producing a prepreg characterized by impregnating decorative paper with melamine resin through a step of impregnating decorative paper that has undergone an intertempering impregnation step (this impregnation step) and satisfying the following formula.
Gel time (seconds) of the main impregnation step-Gel time (seconds) of the inter-paper reinforced impregnation step ≧ 30 (seconds)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2015073212A JP6344612B2 (en) | 2015-03-31 | 2015-03-31 | Manufacturing method of high gloss decorative board |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2015073212A JP6344612B2 (en) | 2015-03-31 | 2015-03-31 | Manufacturing method of high gloss decorative board |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2016190477A JP2016190477A (en) | 2016-11-10 |
JP6344612B2 true JP6344612B2 (en) | 2018-06-20 |
Family
ID=57245189
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2015073212A Active JP6344612B2 (en) | 2015-03-31 | 2015-03-31 | Manufacturing method of high gloss decorative board |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP6344612B2 (en) |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59209865A (en) * | 1983-05-15 | 1984-11-28 | 松下電工株式会社 | Manufacture of decorative board |
CA1251603A (en) * | 1988-03-18 | 1989-03-28 | Roger A. Crawford | Saturating grade paper |
JPH01317714A (en) * | 1988-06-20 | 1989-12-22 | Matsushita Electric Works Ltd | Method for impregnating base material with varnish |
JPH04268341A (en) * | 1991-02-23 | 1992-09-24 | Toshiba Chem Corp | Production of flame-retarding laminate |
JPH10266094A (en) * | 1997-03-24 | 1998-10-06 | Nippon Paper Ind Co Ltd | Laminated plate base paper and its production |
AT500083B1 (en) * | 2003-09-08 | 2009-12-15 | Kaindl Decor Gmbh | DECORLAMINATE AND METHOD FOR THE PRODUCTION THEREOF |
EP2265761B1 (en) * | 2008-03-28 | 2014-10-29 | Depco-Trh Pty Ltd | Method for manufacturing an overlaying material |
-
2015
- 2015-03-31 JP JP2015073212A patent/JP6344612B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
JP2016190477A (en) | 2016-11-10 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3458391A (en) | Plastic laminates | |
RU2612823C2 (en) | Method of printed pattern application on particleboard and particleboard with printed decorative layer | |
KR100918559B1 (en) | Interior product having transfer-printed base layer and process for preparing the same | |
EP2784218A1 (en) | Granulation-free ecological plate high-pressure decorative surface material and manufacturing method thereof | |
JP3789694B2 (en) | Melamine resin decorative sheet | |
EP2093324A1 (en) | Through color high pressure decorative laminate and method of making same | |
US3589974A (en) | Decorative laminate surfaced with a compressed layer of a fibrillated acrylic fiber paper,said paper having been transparentized during a heat and pressure consolidation step and having been substantially free of any impregnating resin | |
JPH0564104B2 (en) | ||
RU2475506C2 (en) | Impregnation with hybrid resins | |
US4871596A (en) | Artificial marble | |
KR100951163B1 (en) | Flame-retardant board and manufacturing method therof | |
KR101327756B1 (en) | Flooring having wear layer by dual cure system and the Method of manufacturing the same | |
Nemli | Factors affecting some quality properties of the decorative surface overlays | |
KR20100025723A (en) | Wood flooring having transfer-printed supporting layer | |
KR102092124B1 (en) | Method for manufacturing flooring plate and flooring plate manufactured by the same | |
JP6344612B2 (en) | Manufacturing method of high gloss decorative board | |
CN109532180B (en) | Non-staining and non-finger-mark high-pressure decorative plate and preparation method thereof | |
Nemli et al. | The resistances of several types of overlaying materials against cigarette burn, scratch, and abrasion | |
US3369960A (en) | Decorative laminates of improved weather resistance | |
US3021239A (en) | Structures comprising a modified diaminotriazine-aldehyde resinous composition | |
US20090220808A1 (en) | Resin composition comprising waste of resin impregnated material | |
KR101792129B1 (en) | Eco-friendly surface finishing material sheet and manufacture method thereof | |
KR102516849B1 (en) | Floor board of corrugated carboard having improved dimensional stability and manufacturing method thereof | |
RU85120U1 (en) | WOODEN GLUED FACED MATERIAL | |
WO2023082987A1 (en) | Solvent-borne acid-curing coating composition and coated article |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20170809 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20180418 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20180426 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20180509 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 6344612 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |