JP2005068202A - Melamine resin composition and melamine decorative board using the same - Google Patents

Melamine resin composition and melamine decorative board using the same Download PDF

Info

Publication number
JP2005068202A
JP2005068202A JP2003209173A JP2003209173A JP2005068202A JP 2005068202 A JP2005068202 A JP 2005068202A JP 2003209173 A JP2003209173 A JP 2003209173A JP 2003209173 A JP2003209173 A JP 2003209173A JP 2005068202 A JP2005068202 A JP 2005068202A
Authority
JP
Japan
Prior art keywords
melamine
resin composition
paper
decorative board
dialkoxyethanal
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
JP2003209173A
Other languages
Japanese (ja)
Inventor
Akihiro Yamamoto
晃広 山本
Yutaka Hori
豊 堀
Naoki Matsumoto
直樹 松本
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 JP2003209173A priority Critical patent/JP2005068202A/en
Publication of JP2005068202A publication Critical patent/JP2005068202A/en
Pending legal-status Critical Current

Links

Abstract

<P>PROBLEM TO BE SOLVED: To provide a melamine resin composition which can be produced in a short time and has improved storability, and to provide a melamine decorative board which releases formaldehyde in a reduced amount. <P>SOLUTION: This melamine resin composition is characterized by reacting melamine with a dialkoxyethanal represented by the formula as an essential component. The melamine is reacted with the dialkoxyethanal in a molar ratio of 1.0 : 0.01 to 2.5 at pH 7.5 to 11. The melamine decorative board is characterized by impregnating a resin solution containing the melamine resin composition as a main component into decorative paper, drying the impregnated paper, laminating the dried paper to a core material, and then subjecting the laminate to a thermocompression molding treatment. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

【0001】
【産業上の利用分野】
本発明は、メラミン樹脂組成物及びこれを用いたメラミン化粧板に関する。
【0002】
【従来技術】
【特許文献1】特表平10−510309
【特許文献2】特開2001−72732
これまでより、住宅の水平面や垂直面にはメラミン化粧板が使用されている。メラミン化粧板には高圧メラミン化粧板と低圧メラミン化粧板に大別され、高圧メラミン化粧板は、メラミン−ホルムアルデヒド縮合物を主な成分とする樹脂液を化粧紙に含浸し、乾燥したメラミン樹脂含浸紙と、フェノール−ホルムアルデヒド縮合物を主な成分とする樹脂液をクラフト紙に含浸し、乾燥したフェノール樹脂含浸コア紙とを必要枚数積層し、成形圧力が40〜120kg/cmで熱圧成形して得られ、耐摩耗性が要求される場合には、表面紙にメラミン−ホルムアルデヒド縮合物を主な成分とする樹脂液を含浸したメラミン樹脂含浸表面紙が用いられる。
また、低圧メラミン化粧板は、合板やパティクルボードなどの構造材を基材とし、樹脂含浸化粧紙を積層し、成形圧力が10〜40kg/cmで熱圧成形して得られる。
【0003】
表面紙や化粧紙に適用される前記のメラミン−ホルムアルデヒド縮合物は、メラミンとホルムアルデヒドをモル比1.0:1.0〜2.8で触媒とともに常圧で数時間加熱しながら攪拌し、適宜溶剤を加え冷却後、無色透明な粘稠な液体として得られる。
また、接着剤用途などで用いる場合は、反応中にアルコールを加え、アルキルエーテル化することが行われている。
【0004】
【発明が解決しようとする課題】
しかしながら、メラミンは粉体であるため、溶解させるのに多量の水を必要とし、低モル比で反応を行うと多量の水を添加するため固形分が低下し、濃縮時間が長くなる上、保存性が劣るなどの欠点があった。これを解消するためモル比を高くするとホルムアルデヒドの放散量が大きくなり、環境への問題が懸念され、モル比に制限があった。
【0005】
【課題を解決するための手段】
本発明はかかる状況に鑑み検討されたもので、化1で示されるジアルコキシエタナールを必須成分として、メラミンと反応させてなることを特徴とするメラミン樹脂組成物、及び該メラミン樹脂組成物を主な成分とする樹脂液を、表面紙、や化粧紙に含浸し、乾燥した後、コア材ともに積層し、熱圧成形してなることを特徴とするメラミン化粧板である。
以下、本発明について詳細に説明する。
【0006】
本発明のメラミン樹脂組成物は、化1で示されるジアルコキシエタナールを必須成分として、メラミンと反応させてなるものである。好ましい割合は、メラミン1モルに対して、ジアルコキシエタナール0.01〜2.5モルであり、ジアルコキシエタナールが下限未満では、ホルムアルデヒド臭の低減、製造時間の短縮に効果がなく、また、上限を超えると反応制御が難しくなり、樹脂の保存安定性が低下する。
このジアルコキシエタナールはその構造上、アルコール溶性を付与できるため、従来接着剤を製造する際に必要とされたメチロール基エーテル化工程を省略することができる。
【0007】
反応させる際には、メラミンの一部をジアルコキシエタナールと共縮合可能な他の化合物、例えば尿素、ベンゾグアナミン、アセトグアナミンなどで置き換えてもよい。
また、ジアルコキシエタナールとホルムアルデヒドを併用してもよく、ホルムアルデヒドは、その一部をパラホルムアルデヒド、ホルムアルデヒド以外のアルデヒド成分、例えばアセトアルデヒドなどの脂肪族アルデヒド類、ベンズアルデヒドなどの芳香族アルデヒド類、フルフラールなど置き換えてもよい。
【0008】
化1で示されるジアルコキシエタナールのR1及びR2は、メチル基、エチル基、n−プロピル基、イソプロピル基、n−ブチル基、sec−ブチル基、イソブチル基、t−ブチル基、n−ペンチル基、n−ヘキシル基等などのアルキル基であり、好ましくはR1及びR2は同じ基で、更に好ましくはn−プロピル又はエチル基、特にメチル基であり、炭素数が少ない程、反応性に富み、難燃性が付与される。
【0009】
反応中のpHは7.5〜11が好ましく、pHが7.5より低いと、メチロールメラミンの縮合が大きくなり、pHが11より高いと、メチロールメラミンとジアルコキシエタナールとの反応が進みにくくなる。
pHを7.5〜11の範囲に調整するには、メラミン、ジアルコキシエタナール、ホルムアルデヒドの反応を妨げないものであればよく、例えば、水酸化ナトリウムの如きアルカリ金属水酸化物が挙げられる。
更に、樹脂保存性を良くするためにメチルアルコール、エチルアルコール、ブチルアルコール等の低級アルコール類によってエーテル化されてもよい。
【0010】
化粧板用化粧紙は、α−セルロ−ス繊維、クラフトパルプ、リンタ−パルプなどの天然繊維のほか、ビニロン繊維、ナイロン繊維、アクリル繊維などの合成繊維から製造された紙基材及び不織布、あるいは天然繊維や合成繊維から作られた織布にグラビア印刷等により柄を設けるか、または着色顔料を抄き込んだ抄造紙であり、樹脂含浸化粧紙は前記のメラミン化粧板用樹脂組成物を主な成分とする樹脂駅を含浸し、乾燥することにより得られる。
【0011】
樹脂含浸コア紙はクラフト紙、不織布、クロスなどの基材にレゾール型のフェノール樹脂を主成分とする樹脂液を含浸し乾燥したフェノール樹脂含浸コア紙が耐水性、耐熱性、強度などに優れ好適に用いられる。
このレゾール型のフェノール樹脂はフェノール類とアルデヒド類を塩基性触媒下で反応させ溶剤を適量加えたもので、フェノール類としては、フェノール、クレゾール、キシレノール、オクチルフェノール、フェニルフェノール、ビスフェノールA、ビスフェノールS、ビスフェノールFなどが挙げられ、アルデヒド類としては、ホルムアルデヒド、パラホルムアルデヒド、グリオキザール、トリオキザールなどが挙げられる。
【0012】
また、必要に応じてパラトルエンスルフォンアミド、桐油、DOP、TCP(トリクレジルホスフェート)などの可塑化を促す変性剤で変性されたものも適用でき、塩基性触媒としては、ナトリウム、カリウムなどのアルカリ金属、及びマグネシウム、カルシウムなどのアルカリ土類金属の酸化物や水酸化物、及びトリエチルアミン、トリエタノールアミンなどのアミン類が挙げられる。
【0013】
化粧層の色、柄を保護するために用いる樹脂含浸表面紙は、坪量20〜150g/mの表面紙に、化粧紙と同様、メラミン化粧板用樹脂組成物を主な成分とする樹脂駅を含浸し、乾燥することにより得られる。
【0014】
実施例1(ジメトキシエタナール)
メラミン樹脂組成物
メラミンとジメトキシエタナールのモル比がそれぞれ1:1.3の配合物を水酸化ナトリウムpH9に調整してメチロール化反応を行なった後、蟻酸を加え、PH7に中和して、水溶性が180%/30℃になるまで反応が行ない、実施例1のメラミン樹脂組成物を得た。
メラミン樹脂含浸表面紙
坪量24g/mの表面紙に、前記のメラミン樹脂組成物を主な成分とする樹脂液を、式1に示す含浸率が含浸率が170%となるように含浸し、乾燥してメラミン樹脂含浸表面紙を得た。
【式1】

Figure 2005068202
メラミン樹脂含浸化粧紙
坪量80g/mの木目柄の化粧紙に、前記のメラミン樹脂組成物を主な成分とする樹脂液を、式1で示す含浸率が100%となるように含浸してメラミン樹脂含浸化粧紙を得た。
フェノール樹脂含浸コア紙
坪量198g/mのクラフト紙にフェノール樹脂を主成分とする樹脂液を、式1に示す含浸率が50%となるように含浸してフェノール樹脂含浸コア紙を得た。
メラミン化粧板
下から順に、フェノール樹脂含浸コア紙を5枚、メラミン樹脂含浸化粧紙を1枚、メラミン樹脂含浸表面紙を1枚積層し、加熱加圧プレス機により、加熱温度138℃、圧力70kg/mの成型条件下で熱圧して、実施例1のメラミン化粧板を得た。
【0015】
実施例2(ジメトキシエタナールとホルムアルデヒドとの併用)
実施例1において、メラミンとジメトキシエタナールとホルムアルデヒドをモル比で1:0.3:1.0で配合した以外は同様に実施して、実施例2のメラミン樹脂組成物、及びメラミン化粧板を得た。
【0016】
実施例3(オーバーレイなし)
実施例2において、坪量100g/mの無地柄の化粧紙を用い、メラミン樹脂含浸表面紙を用いなかった以外は同様に実施して、実施例3のメラミン化粧板を得た。
【0017】
実施例4(ジエトキシエタナールを用いた例)
実施例2において、ジメトキシエタナールに代えてジエトキシエタナールを用いた以外は同様に実施して、実施例4のメラミン樹脂組成物、及びメラミン化粧板を得た。
【0018】
実施例5(接着剤の例)
実施例1で得られたメラミン樹脂組成物を更に脱水し、固形分で75%にして、メラミン接着剤を得た。
【0019】
比較例1(ジメトキシエタナールを用いなかった場合)
実施例1において、ジメトキシエタナールに代えてホルムアルデヒドを用いた以外は同様に実施し、比較例1の樹脂組成物、及び化粧板を得た。
【0020】
比較例2(ジメトキシエタナールのモル比が下限未満の場合)
実施例1において、ジメトキシエタナールのモル比を0.009とした以外は同様に実施した。
【0021】
比較例3(ジメトキシエタナールのモル比が上限を超える場合)
実施例1において、ジメトキシエタナールのモル比を2.6とした以外は同様に実施した。
【0022】
比較例4(pHが下限未満の場合)
実施例1において、反応中のpHを7.0とした以外は同様に実施した。
【0023】
比較例5(pHが上限を超える場合)
実施例1において、反応中のpHを12とした以外は同様に実施した。
【0024】
比較例6(ジメトキシエタナールを用いなかった接着剤の例)
実施例5において、ジメトキシエタナールに代えてホルムアルデヒドを用い、メチロール基エーテル化工程を経た以外は同様に実施して、接着剤を得た。
【0025】
評価結果を表1に示す。
【表1】
Figure 2005068202
【0026】
【発明の効果】
本発明によれば、ジアルコキシエタナールを必須成分として反応させることによりメラミンの溶解量が大幅に向上し、濃縮量減らすことができ、製造時間を短縮できる。
また、完全水系で反応が行えるため、メラミン化粧板を製造する際、成形プレートとして鏡面板を用いた鏡面仕上げにしても綺麗な表面となる。
更に、メラミンとホルムアルデヒドが低モル比で反応でき、樹脂組成物の保存性が向上し、これを用いたメラミン化粧板のホルムアルデヒドの刺激臭も低減できる。
更にまた、表1に示すようにアルコール混和率が高く、溶剤系の樹脂組成物であるため、化粧板用の含浸紙を製造する際、乾燥性が良い。
加えて、製品として、メラミン化粧板を例として記載したが接着剤用途にも使用できる。[0001]
[Industrial application fields]
The present invention relates to a melamine resin composition and a melamine decorative board using the same.
[0002]
[Prior art]
[Patent Document 1] JP-T-10-510309
[Patent Document 2] JP-A-2001-72732
From the past, melamine decorative boards have been used on horizontal and vertical surfaces of houses. The melamine decorative board is broadly divided into a high-pressure melamine decorative board and a low-pressure melamine decorative board. Kraft paper is impregnated with paper and a resin liquid containing phenol-formaldehyde condensate as the main component, and the required number of dried phenol resin-impregnated core papers are laminated, and hot-pressure molding is performed at a molding pressure of 40 to 120 kg / cm 2 When the abrasion resistance is required, a melamine resin-impregnated surface paper impregnated with a resin liquid mainly composed of a melamine-formaldehyde condensate is used.
The low-pressure melamine decorative board is obtained by laminating resin-impregnated decorative paper with a structural material such as plywood or particle board as a base material and hot pressing with a molding pressure of 10 to 40 kg / cm 2 .
[0003]
The melamine-formaldehyde condensate applied to face paper and decorative paper is stirred while heating melamine and formaldehyde at a molar ratio of 1.0: 1.0 to 2.8 together with a catalyst at normal pressure for several hours. After cooling by adding a solvent, it is obtained as a colorless transparent viscous liquid.
Moreover, when using for an adhesive use etc., adding alcohol during reaction and alkylating is performed.
[0004]
[Problems to be solved by the invention]
However, since melamine is a powder, a large amount of water is required to dissolve it. When a reaction is carried out at a low molar ratio, a large amount of water is added, so that the solid content is lowered, the concentration time is increased, and the storage is continued. There were drawbacks such as inferiority. If the molar ratio is increased to solve this problem, the amount of formaldehyde emitted increases, and there are concerns about environmental problems, and the molar ratio is limited.
[0005]
[Means for Solving the Problems]
The present invention has been studied in view of such circumstances, and a dialkoxyethanal represented by Chemical Formula 1 as an essential component is reacted with melamine, and the melamine resin composition is characterized in that A melamine decorative board, which is obtained by impregnating a surface liquid or decorative paper with a resin liquid as a main component, drying, laminating together with a core material, and hot pressing.
Hereinafter, the present invention will be described in detail.
[0006]
The melamine resin composition of the present invention is obtained by reacting dialkoxyethanal represented by Chemical Formula 1 with melamine as an essential component. A preferred ratio is 0.01 to 2.5 moles of dialkoxyethanal per mole of melamine. When dialkoxyethanal is less than the lower limit, there is no effect in reducing formaldehyde odor and shortening the production time. If the upper limit is exceeded, reaction control becomes difficult, and the storage stability of the resin decreases.
Since this dialkoxyethanal can impart alcohol solubility due to its structure, the methylol group etherification step conventionally required when producing an adhesive can be omitted.
[0007]
In the reaction, a part of melamine may be replaced with another compound capable of cocondensing with dialkoxyethanal, for example, urea, benzoguanamine, acetoguanamine and the like.
In addition, dialkoxyethanal and formaldehyde may be used in combination. Part of formaldehyde is paraformaldehyde, aldehyde components other than formaldehyde, for example, aliphatic aldehydes such as acetaldehyde, aromatic aldehydes such as benzaldehyde, furfural, etc. It may be replaced.
[0008]
R1 and R2 of the dialkoxyethanal represented by Chemical Formula 1 are methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group, isobutyl group, t-butyl group, n-pentyl. Group, an alkyl group such as an n-hexyl group, etc., preferably R1 and R2 are the same group, more preferably an n-propyl or ethyl group, especially a methyl group. , Flame retardancy is imparted.
[0009]
The pH during the reaction is preferably 7.5 to 11, and if the pH is lower than 7.5, the condensation of methylol melamine increases, and if the pH is higher than 11, the reaction between methylol melamine and dialkoxyethanal hardly proceeds. Become.
In order to adjust pH to the range of 7.5-11, what is necessary is just the thing which does not prevent reaction of a melamine, dialkoxyethanal, and formaldehyde, For example, alkali metal hydroxide like sodium hydroxide is mentioned.
Furthermore, it may be etherified with lower alcohols such as methyl alcohol, ethyl alcohol, and butyl alcohol in order to improve the resin storage stability.
[0010]
The decorative paper for decorative board is a paper base and non-woven fabric produced from synthetic fibers such as vinylon fibers, nylon fibers, acrylic fibers in addition to natural fibers such as α-cellulose fiber, kraft pulp and linter pulp, or The paper is a paper made by forming a pattern on a woven fabric made of natural fiber or synthetic fiber by gravure printing or the like, or by embedding a coloring pigment, and the resin-impregnated decorative paper is mainly composed of the resin composition for a melamine decorative board. It is obtained by impregnating a resin station as a major component and drying.
[0011]
Resin-impregnated core paper is excellent in water resistance, heat resistance, strength, etc. due to impregnation of a resin liquid mainly composed of resol-type phenol resin on a substrate such as kraft paper, non-woven fabric, cloth, etc. Used for.
This resol type phenolic resin is obtained by reacting phenols and aldehydes in the presence of a basic catalyst and adding an appropriate amount of solvent. As phenols, phenol, cresol, xylenol, octylphenol, phenylphenol, bisphenol A, bisphenol S, Examples include bisphenol F, and examples of aldehydes include formaldehyde, paraformaldehyde, glyoxal, and trioxal.
[0012]
In addition, those modified with a modifying agent that promotes plasticization such as paratoluene sulfonamide, tung oil, DOP, TCP (tricresyl phosphate) can be applied as necessary, and basic catalysts such as sodium and potassium can be used. Examples thereof include oxides and hydroxides of alkali metals and alkaline earth metals such as magnesium and calcium, and amines such as triethylamine and triethanolamine.
[0013]
The resin-impregnated surface paper used to protect the color and pattern of the decorative layer is a resin having a basis weight of 20 to 150 g / m 2 and a resin mainly composed of a resin composition for a decorative melamine board similar to decorative paper. It is obtained by impregnating the station and drying it.
[0014]
Example 1 (Dimethoxyethanal)
Melamine resin composition Melamine and dimethoxyethanal molar ratios of 1: 1.3 each was adjusted to sodium hydroxide pH 9 to perform a methylolation reaction, then added formic acid, neutralized to PH7, The reaction was continued until the water solubility reached 180% / 30 ° C., and the melamine resin composition of Example 1 was obtained.
A melamine resin impregnated surface paper is impregnated on a surface paper having a basis weight of 24 g / m 2 with a resin liquid containing the melamine resin composition as a main component so that the impregnation ratio shown in Formula 1 is 170%. And dried to obtain a melamine resin-impregnated surface paper.
[Formula 1]
Figure 2005068202
Melamine resin impregnated decorative paper impregnated on a wood grain pattern decorative paper with a grammage of 80 g / m 2 so that the impregnation ratio shown in Formula 1 is 100% with a resin liquid mainly composed of the melamine resin composition. Thus, a decorative paper impregnated with melamine resin was obtained.
Phenol resin impregnated core paper Kraft paper having a basis weight of 198 g / m 2 was impregnated with a resin liquid containing phenol resin as a main component so that the impregnation ratio shown in Formula 1 was 50% to obtain a phenol resin impregnated core paper. .
In order from the bottom of the melamine decorative board, 5 sheets of phenol resin-impregnated core paper, 1 sheet of melamine resin-impregnated decorative paper, and 1 sheet of melamine resin-impregnated surface paper are laminated, and the heating temperature is 138 ° C and the pressure is 70 kg. The melamine decorative board of Example 1 was obtained by hot-pressing under the molding conditions of / m 2 .
[0015]
Example 2 (combination of dimethoxyethanal and formaldehyde)
The same procedure as in Example 1 was conducted except that melamine, dimethoxyethanal and formaldehyde were mixed at a molar ratio of 1: 0.3: 1.0, and the melamine resin composition of Example 2 and the melamine decorative board were obtained. Obtained.
[0016]
Example 3 (no overlay)
A melamine decorative board of Example 3 was obtained in the same manner as in Example 2, except that a plain pattern decorative paper having a basis weight of 100 g / m 2 was used and a melamine resin-impregnated surface paper was not used.
[0017]
Example 4 (Example using diethoxyethanal)
In Example 2, it carried out similarly except having used diethoxyethanal instead of dimethoxyethanal, and obtained the melamine resin composition of Example 4, and the melamine decorative board.
[0018]
Example 5 (example of adhesive)
The melamine resin composition obtained in Example 1 was further dehydrated to a solid content of 75% to obtain a melamine adhesive.
[0019]
Comparative Example 1 (when dimethoxyethanal was not used)
In Example 1, it carried out similarly except having used formaldehyde instead of dimethoxyethanal, and the resin composition of the comparative example 1 and the decorative board were obtained.
[0020]
Comparative Example 2 (when the molar ratio of dimethoxyethanal is less than the lower limit)
The same procedure as in Example 1 was performed except that the molar ratio of dimethoxyethanal was changed to 0.009.
[0021]
Comparative Example 3 (when the molar ratio of dimethoxyethanal exceeds the upper limit)
In Example 1, it carried out similarly except having set the molar ratio of dimethoxyethanal to 2.6.
[0022]
Comparative Example 4 (when pH is below the lower limit)
In Example 1, it implemented similarly except having set pH during reaction to 7.0.
[0023]
Comparative Example 5 (when the pH exceeds the upper limit)
In Example 1, it implemented similarly except having made pH during reaction into 12.
[0024]
Comparative Example 6 (Example of adhesive not using dimethoxyethanal)
In Example 5, it replaced with dimethoxyethanal and it carried out similarly except having passed the methylol group etherification process, and obtained adhesives.
[0025]
The evaluation results are shown in Table 1.
[Table 1]
Figure 2005068202
[0026]
【The invention's effect】
According to the present invention, by reacting dialkoxyethanal as an essential component, the amount of melamine dissolved can be greatly improved, the amount of concentration can be reduced, and the production time can be shortened.
In addition, since the reaction can be carried out in a complete water system, when a melamine decorative board is produced, even if it is mirror finished using a mirror board as a molding plate, a beautiful surface is obtained.
Furthermore, melamine and formaldehyde can react at a low molar ratio, the storage stability of the resin composition is improved, and the irritating odor of formaldehyde of the melamine decorative board using this can be reduced.
Furthermore, as shown in Table 1, since it has a high alcohol mixing ratio and is a solvent-based resin composition, it has good drying properties when producing impregnated paper for decorative boards.
In addition, although the melamine decorative board was described as an example as a product, it can also be used for adhesive applications.

Claims (5)

化1で示されるジアルコキシエタナールを必須成分として、メラミンと反応させてなることを特徴とするメラミン樹脂組成物。
Figure 2005068202
(式中、R1及びR2はC1〜C8のアルキル基)
A melamine resin composition comprising a dialkoxyethanal represented by Chemical Formula 1 as an essential component and reacted with melamine.
Figure 2005068202
(Wherein R1 and R2 are C1-C8 alkyl groups)
該メラミンと該ジアルコキシエタナールのモル比が1.0:0.01〜2.5で、pH7.5〜11で反応させることを特徴とする請求項1記載のメラミン樹脂組成物。2. The melamine resin composition according to claim 1, wherein the molar ratio of the melamine to the dialkoxyethanal is 1.0: 0.01 to 2.5 and the reaction is performed at pH 7.5 to 11. 3. 該ジアルコキシエタナールがジメトキシエタナールであることを特徴とする請求項1又は2記載のメラミン樹脂組成物。The melamine resin composition according to claim 1 or 2, wherein the dialkoxyethanal is dimethoxyethanal. 該メラミン樹脂組成物を主な成分とする樹脂液を、化粧紙に含浸し、乾燥した後、コア材とともに積層し、熱圧成形してなることを特徴とするメラミン化粧板。A melamine decorative board comprising a decorative liquid impregnated with a resin liquid containing the melamine resin composition as a main component, dried, laminated with a core material, and hot-press molded. 該メラミン樹脂組成物を主な成分とする樹脂液を、表面紙、化粧紙の少なくとも一方に含浸し、乾燥した後、コア材ともに積層し、熱圧成形してなることを特徴とするメラミン化粧板。A melamine makeup comprising a resin liquid containing the melamine resin composition as a main component impregnated in at least one of a surface paper and a decorative paper, dried, laminated with a core material, and hot-press molded. Board.
JP2003209173A 2003-08-28 2003-08-28 Melamine resin composition and melamine decorative board using the same Pending JP2005068202A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2003209173A JP2005068202A (en) 2003-08-28 2003-08-28 Melamine resin composition and melamine decorative board using the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2003209173A JP2005068202A (en) 2003-08-28 2003-08-28 Melamine resin composition and melamine decorative board using the same

Publications (1)

Publication Number Publication Date
JP2005068202A true JP2005068202A (en) 2005-03-17

Family

ID=34402195

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2003209173A Pending JP2005068202A (en) 2003-08-28 2003-08-28 Melamine resin composition and melamine decorative board using the same

Country Status (1)

Country Link
JP (1) JP2005068202A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009537685A (en) * 2006-05-24 2009-10-29 クラリアント スペシャルティー ファイン ケミカルズ(フランス) Amino or phenolic resins based on at least one glyoxal monoacetal and glyoxylic acid and use thereof
WO2011161618A1 (en) * 2010-06-25 2011-12-29 Firmenich Sa Stable formaldehyde-free microcapsules
KR101536490B1 (en) * 2010-11-30 2015-07-13 스미또모 베이크라이트 가부시키가이샤 Decorative melamine board

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009537685A (en) * 2006-05-24 2009-10-29 クラリアント スペシャルティー ファイン ケミカルズ(フランス) Amino or phenolic resins based on at least one glyoxal monoacetal and glyoxylic acid and use thereof
WO2011161618A1 (en) * 2010-06-25 2011-12-29 Firmenich Sa Stable formaldehyde-free microcapsules
CN102958507A (en) * 2010-06-25 2013-03-06 弗门尼舍有限公司 Stable formaldehyde-free microcapsules
CN102958507B (en) * 2010-06-25 2014-08-27 弗门尼舍有限公司 Stable formaldehyde-free microcapsules
US8835002B2 (en) 2010-06-25 2014-09-16 Firmenich Sa Stable formaldehyde-free microcapsules
US9359464B2 (en) 2010-06-25 2016-06-07 Firmenich Sa Stable formaldehyde-free microcapsules
KR101536490B1 (en) * 2010-11-30 2015-07-13 스미또모 베이크라이트 가부시키가이샤 Decorative melamine board
US10279571B2 (en) 2010-11-30 2019-05-07 Sumitomo Bakelite Company Limited Decorative melamine board

Similar Documents

Publication Publication Date Title
US4405690A (en) Polyethylene glycol modified melamine aldehyde resin and postformable laminate made therewith
US6001925A (en) Melamine-formaldehyde resins modified with dicyandiamide and sorbitol for impregnation of substrates for post-formable decorative laminates
JP2005068202A (en) Melamine resin composition and melamine decorative board using the same
JPS59207236A (en) Laminated board difficult to warp and manufacture thereof and resin composition for manufacturing said laminated board
JP6006515B2 (en) Melamine decorative board
US3194720A (en) Melamine laminating resin modified with an anhydride of sorbitol
US4043984A (en) Aminoplasts elasticized with benzoic acid esters
US3897589A (en) Fast curing, water-resistant laminate made with accelerated melamine-aldehyde resin and accelerated phenol-aldehyde resin and method of making it
JP3448112B2 (en) Structural material, method of manufacturing structural material, and interior material for vehicle
WO1998050467A1 (en) Resin composition and board made by using the same
JP3383367B2 (en) Structural material
US4011280A (en) Process for the production of binders for weather-proof wood materials and product
EP0309475B1 (en) Process for the preparation of a phenol-based resin for the production of laminates
JP3383368B2 (en) Structural material
JP2008073979A (en) Melamine decorative plate
US7244504B2 (en) Phenol-free decorative laminates and method of producing the same
JP6629561B2 (en) Manufacturing method of post-form decorative board
WO2007111501A1 (en) Process for the preparation of an aminoplast resin
JPH10279715A (en) Flame-retardant phenolic resin laminate
JP3851508B2 (en) MELAMINE RESIN MOLDED MATERIAL, LAMINATE, AND MELAMINE RESIN MOLDED MOLDING METHOD
JP2022147272A (en) Method for producing kraft lignin-containing phenolic resin
US7235303B2 (en) Phenol-free decorative laminates and method of producing the same
JPH10286925A (en) Flame retardant phenol resin laminate
JP2006110932A (en) Nonflammable decorative board
CN117360013A (en) Gummed paper, LPM impregnated paper, inorganic material environment-friendly processing board containing same and manufacturing method