JP2001263699A - Surface finish material for heater - Google Patents

Surface finish material for heater

Info

Publication number
JP2001263699A
JP2001263699A JP2000083137A JP2000083137A JP2001263699A JP 2001263699 A JP2001263699 A JP 2001263699A JP 2000083137 A JP2000083137 A JP 2000083137A JP 2000083137 A JP2000083137 A JP 2000083137A JP 2001263699 A JP2001263699 A JP 2001263699A
Authority
JP
Japan
Prior art keywords
resin
surface finishing
impregnated
heating heater
sheet material
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
JP2000083137A
Other languages
Japanese (ja)
Inventor
Nobuaki Uenishi
延明 上西
Hideshi Yanagi
秀史 柳
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.)
Bridgestone Corp
Original Assignee
Bridgestone Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bridgestone Corp filed Critical Bridgestone Corp
Priority to JP2000083137A priority Critical patent/JP2001263699A/en
Publication of JP2001263699A publication Critical patent/JP2001263699A/en
Pending legal-status Critical Current

Links

Landscapes

  • Domestic Hot-Water Supply Systems And Details Of Heating Systems (AREA)
  • Laminated Bodies (AREA)

Abstract

PROBLEM TO BE SOLVED: To improve an anti-scar characteristic and make a rising time for a heating operation fast. SOLUTION: A surface finish material 10 for a heater arranged at a surface side of a panel-type heater 3 is constructed such that a resin immersing sheet material 2 containing glass fiber is overlapped on the rear surface of a resin immersing ornamental material 1, and then the resin is immersed and solidified at an entire or a part of the sheet material 2 and the ornamental material 1.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】この発明は、床暖房及び壁暖
房に使用される暖房ヒータの表面側に設けられる暖房ヒ
ータ用表面仕上材に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a surface finishing material for a heating heater provided on a surface side of a heating heater used for floor heating and wall heating.

【0002】[0002]

【従来の技術】床暖房及び壁暖房の表面仕上材に関して
は、例えば床暖房の場合、合板等の表面に薄い化粧材を
貼った積層仕上材、いわゆるフローリング、あるいは、
コルク、畳、塩ビシート、塩ビタイル、カーペットが広
く用いられているが、近年ダニの発生防止や、廃棄時の
環境汚染防止等の観点からフローリングが急速に増加し
てきている。
2. Description of the Related Art With regard to surface finishing materials for floor heating and wall heating, for example, in the case of floor heating, a laminated finishing material in which a thin decorative material is stuck on the surface of plywood or the like, so-called flooring, or
Corks, tatami mats, PVC sheets, PVC tiles, and carpets are widely used, but flooring has been rapidly increasing in recent years from the viewpoint of preventing the occurrence of mites and preventing environmental pollution at the time of disposal.

【0003】[0003]

【発明が解決しようとする課題】床暖房及び壁暖房の表
面仕上材として、フローリングを使用した場合、用途上
物に接触することが多く、その為、仕上材の表面に傷
(特にヘコミ)がつき、外観が悪くなる欠点があった。
特に化粧材が突き板、紙等のようなものの場合、ヘコミ
による表面の破れ等が防止できなかった。また、仕上材
の標準的な厚さが12mmもあり、それ自身が断熱性を
もつため、熱源を入れてから設定温度に達するまでに要
する時間、いわゆる立上り時間が遅くなるとともに、運
転中のエネルギー損失が大きい要因となっていた。
When flooring is used as a surface finishing material for floor heating and wall heating, the flooring often comes into contact with an object in use, and therefore, the surface of the finishing material is damaged (especially dents). There was a drawback that the appearance deteriorated.
In particular, when the decorative material is a veneer, paper, or the like, it is impossible to prevent the surface from being broken due to dents. In addition, the standard thickness of the finishing material is as large as 12 mm, and since the material itself has heat insulating properties, the time required from when a heat source is turned on until the set temperature is reached, that is, the so-called rise time is delayed, and energy during operation is reduced. Loss was a major factor.

【0004】そこでこの発明は、化粧材が薄板あるいは
軟質材であっても、仕上材として傷のつきにくい耐傷性
に優れた材料にするとともに、仕上材の厚さを薄くして
暖房の立上り時間を速くし、かつ省エネルギー化になる
表面仕上材を安価に提供することを目的とする。
[0004] Therefore, the present invention is to provide a finish material that is resistant to scratches and has excellent scratch resistance even if the decorative material is a thin plate or a soft material, and that the thickness of the finish material is reduced to increase the heating start-up time. It is an object of the present invention to provide a surface finishing material that saves energy and saves energy at low cost.

【0005】[0005]

【課題を解決するための手段】上述の目的を達成するた
め、この発明は、パネル型の暖房ヒータの表面側に設け
られる暖房ヒータ用表面仕上材において、樹脂浸透性の
ある化粧材の裏面にガラス繊維を含む樹脂浸透性のある
シート材を重ね合わせ、シート材及び化粧材の全部又は
一部に樹脂が含浸固化されているものである。
In order to achieve the above-mentioned object, the present invention relates to a heating heater surface finishing material provided on the front side of a panel-type heating heater. A resin-permeable sheet material containing glass fibers is superposed, and the resin is impregnated and solidified in all or a part of the sheet material and the decorative material.

【0006】[0006]

【発明の実施の形態】以下に、この発明の好適な実施例
を図面を参照にして説明する。
Preferred embodiments of the present invention will be described below with reference to the accompanying drawings.

【0007】図1に示す実施例は、浸透性のある化粧材
1の裏面にガラス繊維を含む浸透性のあるシート材2を
重ね合わせ、シート材2及び化粧材1の全部又は一部に
樹脂が含浸固化された表面仕上材10を示す。この表面
仕上材10は、パネル型の暖房ヒータ3上に設けられ
る。化粧材1としては、突き板例えばナラ単板(厚さ
0.3mm〜1.0mm程度)、紙が好適に使用でき
る。紙に木目を印刷し木目に沿って凹凸加工を施したも
のは質感もあり、化粧材1として好適に使用できる。シ
ート材2を形成するガラス繊維は、織布、不織布、ネッ
ト状のものを用いることができ、特に不織布に関して
は、繊維原料として3〜50mmにカットされた繊維を
湿式抄紙、もしくは乾式不織布製造法によりシート材化
したものをバインダー樹脂で結合したものが好適に使用
できる。ガラス繊維の長さも3mm未満の短繊維では、
補強効果が低く、一方50mmを越える長繊維では、均
一シート化が困難であり、結果として優れた補強効果が
得られない。また、3〜15mmの短繊維が全繊維中2
0〜100%であることが、強度(補強性)、不織布の
均一性の観点からは好ましい。短繊維が20%より少な
いと不織布の均一性が図れない。これら繊維材料の他に
短繊維のセルロースパルプ等を混合することは差し支え
ない。また、ガラス繊維を用いる場合は、繊維表面をシ
ランカップリング剤でコートしておくことにより、補強
効果を高めることができる。ガラス繊維を含む不織布
は、原料繊維を接着もしくは絡み合わせ或いはその双方
を用いて機械的、化学的、加熱的もしくは溶媒を用いる
方法、或いはそれらの組合せによってシート状に形成さ
れる。また、含浸性、脱泡性、シート基材強度、ハンド
リング、成形品の耐傷性の点から、坪量として50〜2
00g/m2が望ましい。ガラス不織布は、坪量が50
g/m2より少ないと、耐傷性が発現しにくく、200
g/m2より多いと、樹脂の含浸が困難となる。このよ
うな化粧材1及びシート材2に含浸され固化される樹脂
としては、例えば、フェノール類とアルデヒド類との反
応により得られるフェノール樹脂、末端に反応性のエポ
キシ基を持つオリゴマーに硬化剤を添加して得られるエ
ポキシ樹脂、ユリア樹脂、ウレタン樹脂が例示でき、さ
らにこれらに各種の充填剤、例えばステアリン酸鉛、ジ
ブチル錫ジラウレート、カーボンブラック、炭酸カルシ
ウム、チタンホワイト、雲母、ガラス球、水酸化アルミ
ニウム、酸化アンチモン、トリ(2,3ジプロモプロピ
ル)ホスフェート、脂肪酸スルフォン酸塩、高級アルコ
ール硫酸エステル等、熱安定剤、強化剤、難燃剤、帯電
防止剤等が配合されて使用される。また、熱硬化性樹脂
にフェノール樹脂を選んだ場合、樹脂の製造に必要な触
媒としては、アルキルアミン、アンモニア、水酸化ナト
リウム、水酸化バリウム等が好ましい。特に、アルキル
アミン、アンモニアについては他の2つに比べ分子量も
大きく、分子構造上、水和性が低いので貼り合わせ後の
耐水性が飛躍的に向上する。この時、フェノール樹脂
は、固形分20〜80%となるように水又はアルコール
(アルコールの場合は沸点が低く乾燥しやすいからMe
OHが好ましい)に溶解もしくは分散されていることが
含浸の容易さの点から好ましい。固形分が20%未満だ
と必要量含浸することが困難となり、80%より多いと
粘度上昇により含浸が困難となる。また、ガラス繊維へ
含浸させる樹脂は、対繊維比率(重量比)50%以上含
有し、望ましくは100〜300%である。またシート
材2への含浸時において、固形分50〜500g/
2、好ましくは150〜350g/m2になるようにす
ることが好ましい。50g/m2未満だと充分な耐傷性
を発現しにくく、500g/m2以下でなければ硬化時
間がかかり、端部からのはみだし等外観上も問題があ
る。
In the embodiment shown in FIG. 1, a permeable sheet material 2 containing glass fiber is superimposed on the back surface of a permeable material 1, and resin is applied to all or a part of the sheet material 2 and the decorative material 1. Shows the surface finish 10 impregnated and solidified. The surface finishing material 10 is provided on the panel-type heating heater 3. As the decorative material 1, a veneer such as a veneer veneer (thickness of about 0.3 mm to 1.0 mm) or paper can be suitably used. A material obtained by printing wood grain on paper and performing unevenness processing along the wood grain has a texture and can be suitably used as the decorative material 1. The glass fiber forming the sheet material 2 may be a woven fabric, a nonwoven fabric, or a net-like glass fiber. In particular, regarding the nonwoven fabric, a fiber cut into 3 to 50 mm as a fiber raw material is prepared by wet papermaking or dry nonwoven fabric production. In this case, those formed into sheet materials and bonded with a binder resin can be suitably used. For short fibers with a glass fiber length of less than 3 mm,
On the other hand, with a long fiber exceeding 50 mm, it is difficult to form a uniform sheet, and as a result, an excellent reinforcing effect cannot be obtained. In addition, short fibers of 3 to 15 mm account for 2% of all fibers.
It is preferable that it is 0 to 100% from the viewpoint of strength (reinforcing property) and uniformity of the nonwoven fabric. If the short fibers are less than 20%, uniformity of the nonwoven fabric cannot be achieved. Mixing short fiber cellulose pulp or the like in addition to these fiber materials may be used. When glass fibers are used, the reinforcing effect can be enhanced by coating the fiber surfaces with a silane coupling agent. The nonwoven fabric containing glass fibers is formed into a sheet by a method of mechanically, chemically, thermally or using a solvent by bonding and / or entanglement of raw fibers, or a combination thereof. Further, from the viewpoint of impregnation, defoaming, sheet base strength, handling, and scratch resistance of the molded product, the basis weight is 50 to 2
00 g / m 2 is desirable. Glass nonwoven fabric has a basis weight of 50
When the amount is less than g / m 2 , scratch resistance is hardly developed and 200
If the amount is more than g / m 2 , it becomes difficult to impregnate the resin. Examples of the resin which is impregnated into the decorative material 1 and the sheet material 2 and solidified are, for example, a phenol resin obtained by a reaction between a phenol and an aldehyde, and a curing agent for an oligomer having a reactive epoxy group at a terminal. Examples thereof include an epoxy resin, a urea resin, and a urethane resin obtained by addition, and further include various fillers such as lead stearate, dibutyltin dilaurate, carbon black, calcium carbonate, titanium white, mica, glass spheres, and hydroxide. Aluminum, antimony oxide, tri (2,3 dibromopropyl) phosphate, fatty acid sulfonates, higher alcohol sulfates, etc., heat stabilizers, reinforcing agents, flame retardants, antistatic agents and the like are used in combination. When a phenol resin is selected as the thermosetting resin, alkylamine, ammonia, sodium hydroxide, barium hydroxide, and the like are preferable as a catalyst required for producing the resin. In particular, alkylamine and ammonia have larger molecular weights than the other two, and have low hydration properties in terms of molecular structure, so that the water resistance after bonding is remarkably improved. At this time, the phenol resin is dissolved in water or alcohol (in the case of alcohol, the boiling point is low and it is easy to dry) so that the solid content becomes 20 to 80%.
OH is preferred) in terms of ease of impregnation. If the solid content is less than 20%, it becomes difficult to impregnate the required amount, and if it is more than 80%, the impregnation becomes difficult due to an increase in viscosity. The resin to be impregnated into the glass fibers contains at least 50% by weight of the fiber (weight ratio), and preferably 100 to 300%. When impregnating the sheet material 2, the solid content is 50 to 500 g /
m 2 , preferably 150 to 350 g / m 2 . If it is less than 50 g / m 2, it is difficult to develop sufficient scratch resistance, and if it is less than 500 g / m 2 , it takes a long time to cure and there is a problem in appearance such as protruding from an end.

【0008】上述の如くガラス繊維に樹脂溶液を含浸さ
せた後、一定条件下で乾燥させて樹脂を半硬化状態にす
る。すなわちプリプレグ化する。プリプレグは、繊維補
強材と熱硬化性樹脂、その他必要に応じ熱可塑性樹脂、
着色剤、硬化触媒等を混和してなる強化プラスチック
の、接着性と成形性の能力を残した硬化終了前の半硬化
状態の成形素材であり、好ましいゲルタイムは150℃
で30〜800秒である。
After the glass fiber is impregnated with the resin solution as described above, the resin is dried under a certain condition to bring the resin into a semi-cured state. That is, the prepreg is formed. Prepreg is a fiber reinforced material and thermosetting resin, other thermoplastic resin as needed,
It is a molding material in a semi-cured state before the completion of curing, which retains adhesiveness and moldability of a reinforced plastic obtained by mixing a coloring agent, a curing catalyst, etc., and has a preferable gel time of 150 ° C.
30 to 800 seconds.

【0009】ガラス繊維に含浸させた熱硬化性樹脂を、
含浸後半硬化状態にするための乾燥条件として、プリプ
レグ状態の溶媒含有率を3〜15重量%、さらには5〜
10重量%にすることが好ましく、3重量%未満では化
粧材1との接着不良をおこし、15重量%以下でない場
合は、プリプレグ同士ブロッキングをおこす。90〜1
20℃の温度で乾燥時間2.5〜20分で好ましい半硬
化状態のプリプレグを得ることができる。
The thermosetting resin impregnated in the glass fiber is
As the drying conditions for setting the cured state in the latter half of the impregnation, the solvent content in the prepreg state is 3 to 15% by weight, more preferably 5 to 15% by weight.
The content is preferably set to 10% by weight, and if it is less than 3% by weight, poor adhesion to the decorative material 1 occurs, and if it is not less than 15% by weight, prepreg blocking occurs. 90-1
A preferable semi-cured prepreg can be obtained at a temperature of 20 ° C. and a drying time of 2.5 to 20 minutes.

【0010】プリプレグの引張強度としては、充分な耐
傷性発現のためには、破断強度10kgf/cm2以上
であることが好ましい。10kgf/cm2未満では充
分な耐傷性が発現しない。破断強度の測定は、プリプレ
グを2枚の離型紙間に挟み、150℃、5分、10kg
f/cm2の条件下で熱プレスして樹脂を硬化させた後
のものについて行った。
[0010] The tensile strength of the prepreg is preferably 10 kgf / cm 2 or more in order to sufficiently develop scratch resistance. If it is less than 10 kgf / cm 2 , sufficient scratch resistance will not be exhibited. The measurement of the breaking strength is as follows. The prepreg is sandwiched between two release papers, 150 ° C., 5 minutes, 10 kg
The test was performed after the resin was cured by hot pressing under the condition of f / cm 2 .

【0011】上述のようにしてガラス繊維に半硬化状態
の熱硬化性樹脂を含浸させたプリプレグを化粧材1の裏
面に重ね合わせ、熱プレスする場合の条件としては、温
度130℃〜180℃が好ましく、さらには140〜1
60℃が好ましい。130℃より低いと樹脂の硬化が充
分でなく、180℃より高いと樹脂の硬化が速すぎて化
粧材1との接触が不充分となり、かつ化粧材1に木質系
材料を用いた場合には反りも大きくなってしまうためで
ある。また、圧力としては、1〜30kgf/cm2
好ましく、1kgf/cm2より低いと樹脂の化粧材1
へのしみ出しが充分でないために接着力が低下し、30
kgf/cm2より大きいと化粧材1の反りが大きくな
る等の不都合が生ずる。さらにまた、プレス時間として
は、2.5〜20分間が好ましく、さらに好ましくは3
〜12.5分である。2.5分より短いと樹脂の硬化が
充分ではなく、20分より長いと樹脂の劣化が生じ、化
粧材1の反りも大きくなる。
As described above, when the prepreg in which the glass fiber is impregnated with the thermosetting resin in a semi-cured state is superimposed on the back surface of the decorative material 1 and hot pressed, the condition is a temperature of 130 ° C. to 180 ° C. Preferably, furthermore 140-1
60 ° C. is preferred. If the temperature is lower than 130 ° C., the curing of the resin is not sufficient. If the temperature is higher than 180 ° C., the curing of the resin is too fast and the contact with the decorative material 1 becomes insufficient. This is because the warpage increases. As the pressure is preferably 1~30kgf / cm 2, of 1 kgf / cm lower than 2 and resin decorative material 1
Adhesion decreases due to insufficient bleeding
If it is larger than kgf / cm 2 , inconveniences such as an increase in warpage of the decorative material 1 occur. Further, the pressing time is preferably 2.5 to 20 minutes, more preferably 3 to 20 minutes.
~ 12.5 minutes. If the time is shorter than 2.5 minutes, the curing of the resin is not sufficient, and if the time is longer than 20 minutes, the resin is deteriorated and the warp of the decorative material 1 is increased.

【0012】ガラス繊維を含む織布又は不織布を単独で
用い、これに半硬化状態の熱硬化性樹脂を含浸させたも
の(プリプレグ)を単独で用いず、例えばこれを複数枚
用いたり紙に熱硬化性樹脂を含浸させたものに上記プリ
プレグを貼り合わせたものを用いることもできる。例え
ば、未硬化のフェノール樹脂を紙に含浸させ、これに上
記プリプレグを貼り合わせたものを用いれば全体の強度
や寸法安定性が飛躍的に向上する。
A woven or non-woven fabric containing glass fibers is used alone, and a material impregnated with a semi-cured thermosetting resin (prepreg) is not used alone. A material obtained by laminating the prepreg on a material impregnated with a curable resin can also be used. For example, if the uncured phenol resin is impregnated into paper and the prepreg is bonded to the paper, the overall strength and dimensional stability are dramatically improved.

【0013】化粧材1の裏面にシート材2を重ね合わせ
て固着したものを図1に示し、この図1に示すものに金
属板4を接着したものを図2に示すが、いずれの場合で
も例えば、シート材2としてガラス不織布を用い、この
ガラス不織布の全部又は一部に固形分50〜500g/
2となるようにフェノール樹脂溶液を含浸させ、含浸
後に所定温度と時間で乾燥させてフェノール樹脂を半硬
化状態(プリプレグ状態)とし、このガラス不織布に含
浸させたフェノール樹脂が半硬化状態にあるとき化粧材
1と重ね合わせたものを使用できる。図1に示す表面仕
上材10では、化粧材1の裏面に樹脂が半硬化状態のガ
ラス不織布を重ね合わせた後に、熱プレスして樹脂を化
粧材1に含浸せしめ固化させる。図2に示す表面仕上材
10では、化粧材1とシート材2とが固着した後にシー
ト材2の裏面に金属板4を接着する。表面仕上材10の
厚さは1mm以下とすることもでき、厚くとも3mm以
下が好ましい。厚さを3mm以下とすることにより、暖
房の立上り時間を速くすることができる。表面仕上材1
0の厚さを薄くしても、プリプレグを用いることで強
度、耐傷性に優れる。また、薄くすることで、運転中の
熱源の温度を低くすることができ、省エネルギーを達成
できる。
FIG. 1 shows a sheet material 2 on which a sheet material 2 is superimposed and fixed on the back surface of a decorative material 1, and FIG. 2 shows a sheet obtained by bonding a metal plate 4 to the sheet material shown in FIG. For example, a glass nonwoven fabric is used as the sheet material 2, and a solid content of 50 to 500 g /
impregnated with a phenol resin solution so as to obtain m 2, and after the impregnation, dried at a predetermined temperature and time to make the phenol resin in a semi-cured state (prepreg state), and the phenol resin impregnated in the glass nonwoven fabric is in a semi-cured state. Sometimes, a material that is superimposed on the cosmetic material 1 can be used. In the surface finishing material 10 shown in FIG. 1, the resin is impregnated into the decorative material 1 by hot pressing after the glass nonwoven fabric in which the resin is in a semi-cured state is overlaid on the back surface of the decorative material 1. In the surface finishing material 10 shown in FIG. 2, the metal plate 4 is bonded to the back surface of the sheet material 2 after the decorative material 1 and the sheet material 2 are fixed. The thickness of the surface finishing material 10 can be 1 mm or less, and preferably 3 mm or less at most. By setting the thickness to 3 mm or less, the rise time of heating can be shortened. Surface finishing material 1
Even if the thickness of 0 is reduced, the use of the prepreg provides excellent strength and scratch resistance. In addition, by reducing the thickness, the temperature of the heat source during operation can be lowered, and energy saving can be achieved.

【0014】図1に示す表面仕上材10において、フェ
ノール樹脂等の樹脂含有量は、30重量%以上含有し、
好ましくは60〜150重量%である。
In the surface finishing material 10 shown in FIG. 1, the content of resin such as phenol resin is 30% by weight or more.
Preferably it is 60 to 150% by weight.

【0015】化粧材1としては厚さ0.3mmのナラ単
板を使用し、シート材2は繊維長3mmのガラス繊維か
らなる坪量100g/m2の不織布を用い、固着後の化
粧材1とシート材2における樹脂含有量が30重量%と
なるようにこのガラス不織布全体にフェノール樹脂を含
浸させ、一定条件下でプリプレグ状態とし、化粧材1の
裏面にプリプレグ状態で樹脂が含浸されたガラス不織布
を重ね合わせ、次いで熱プレスして化粧材1とシート材
2とが固着したものを実施例1とした。また、ガラス繊
維長を12mmとし、その他の条件は実施例1と同様に
して製造したものを実施例2とした。フェノール樹脂の
含有量を100重量%とし、その他の条件は実施例1と
全く同一にして製造したものを実施例3とした。ガラス
繊維長12mm、樹脂含有量100重量%とし、その他
の条件は実施例1と全く同一にして製造したものを実施
例4とした。樹脂含有量150重量%とし、その他の条
件は実施例4と同一にして製造したものを実施例5とし
た。さらに、基材5(厚さ12mmの合板)に直接化粧
材1(厚さ0.3mmのナラ単板)を尿素・メラミン系
の接着剤で接着したものを比較例1とした(図3参
照)。
A veneer veneer having a thickness of 0.3 mm is used as the decorative material 1 and a nonwoven fabric having a basis weight of 100 g / m 2 made of glass fiber having a fiber length of 3 mm is used as the sheet material 2. The glass nonwoven fabric is impregnated with a phenolic resin so that the resin content in the sheet material 2 becomes 30% by weight, the prepreg is formed under a certain condition, and the resin is impregnated on the back surface of the decorative material 1 in the prepreg state. Example 1 was obtained by laminating nonwoven fabrics and then hot pressing to fix the decorative material 1 and the sheet material 2 together. In addition, the glass fiber length was 12 mm, and the other conditions were the same as those of Example 1 to manufacture Example 2. Example 3 was manufactured in the same manner as in Example 1 except that the content of the phenol resin was 100% by weight. A glass fiber length of 12 mm, a resin content of 100% by weight, and the other conditions were exactly the same as those of Example 1, and were manufactured as Example 4. Example 5 was manufactured in the same manner as in Example 4 except that the resin content was 150% by weight. Further, Comparative Example 1 was obtained by directly bonding the decorative material 1 (0.3 mm thick veneer veneer) directly to the base material 5 (12 mm thick plywood) with a urea-melamine adhesive (see FIG. 3). ).

【0016】これら実施例1ないし5と比較例に対しJ
IS K−5400に基づき鉛筆のひっかき値のテスト
を行った。その結果は次の表1に示す通りであった。鉛
筆ひっかき値において評価が「H」は×、「2H」は
△、「3H」は○、「4H以上」は◎として評価した。
◎、○、△、×の順に評価は悪くなる。
In Examples 1 to 5 and Comparative Example, J
A pencil scratch test was performed based on IS K-5400. The results were as shown in Table 1 below. In the pencil scratch value, “H” was evaluated as “X”, “2H” as “Δ”, “3H” as “○”, and “4H or more” as “◎”.
The evaluation becomes worse in the order of ◎, ○, Δ, ×.

【0017】[0017]

【表1】 [Table 1]

【0018】[0018]

【発明の効果】以上説明したように、この発明によれ
ば、パネル型の暖房ヒータの表面側に設けられる暖房ヒ
ータ用表面仕上材において、樹脂浸透性のある化粧材の
裏面にガラス繊維を含む樹脂浸透性のあるシート材を重
ね合わせ、シート材及び化粧材の全部又は一部に樹脂が
含浸固化され、化粧材に樹脂が含浸されているので、表
面に傷、ヘコミがつきにくくなり、シート材にも樹脂が
含浸されガラス繊維が強度を向上させている。また、仕
上材の厚さを極端に薄くしたことで、床暖房及び壁暖房
の立上り時間を速くするとともに、運転中の熱源の温度
を低くすることができ、省エネルギー化になる。
As described above, according to the present invention, in the surface finishing material for a heater provided on the front side of the panel-type heating heater, the back surface of the resin-permeable decorative material contains glass fibers. A resin material permeable sheet material is overlaid, resin is impregnated and solidified in all or part of the sheet material and the decorative material, and the cosmetic material is impregnated with the resin. The resin is also impregnated in the material, and the glass fiber improves the strength. In addition, by extremely reducing the thickness of the finishing material, the rise time of floor heating and wall heating can be shortened, and the temperature of the heat source during operation can be reduced, resulting in energy saving.

【図面の簡単な説明】[Brief description of the drawings]

【図1】表面仕上材の断面図。FIG. 1 is a cross-sectional view of a surface finishing material.

【図2】金属板を用いた表面仕上材の断面図。FIG. 2 is a cross-sectional view of a surface finishing material using a metal plate.

【図3】比較例の断面図。FIG. 3 is a sectional view of a comparative example.

【符号の説明】[Explanation of symbols]

1 化粧材 2 シート材 3 暖房ヒータ 4 金属板 DESCRIPTION OF SYMBOLS 1 Cosmetic material 2 Sheet material 3 Heater 4 Metal plate

フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) B32B 33/00 B32B 33/00 Fターム(参考) 3L073 BB02 BD03 4F100 AB01C AG00B AK01A AK01B AK33A AK33B AK36A AK36B AK51A AK51B AK53A AK53B AP00A AP01 AT00B BA02 BA03 BA07 BA10A BA10C DG01B DG10A DG12 DG13 DG15 DH01 DH01B EJ08 EJ17 EJ42 EJ82 EJ82A EJ82B EJ86 GB08 HB00 HB00A HB31 JK01 JK14Continued on the front page (51) Int.Cl. 7 Identification code FI Theme coat II (Reference) B32B 33/00 B32B 33/00 F term (Reference) 3L073 BB02 BD03 4F100 AB01C AG00B AK01A AK01B AK33A AK33B AK36A AK36B AK51A AK51B AK53A AK53A AK53A AK53A AK53A AP01 AT00B BA02 BA03 BA07 BA10A BA10C DG01B DG10A DG12 DG13 DG15 DH01 DH01B EJ08 EJ17 EJ42 EJ82 EJ82A EJ82B EJ86 GB08 HB00 HB00A HB31 JK01 JK14

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 パネル型の暖房ヒータの表面側に設けら
れる暖房ヒータ用表面仕上材において、 樹脂浸透性のある化粧材の裏面にガラス繊維を含む樹脂
浸透性のあるシート材を重ね合わせ、シート材及び化粧
材の全部又は一部に樹脂が含浸固化されていることを特
徴とする暖房ヒータ用表面仕上材。
1. A heating heater surface finishing material provided on the front side of a panel-type heating heater, wherein a resin-permeable sheet material containing glass fiber is superimposed on the back surface of a resin-permeable cosmetic material, A surface finishing material for a heating heater, wherein a resin is impregnated and solidified in all or a part of the material and the decorative material.
【請求項2】 パネル型の暖房ヒータの表面側に設けら
れる暖房ヒータ用表面仕上材において、 樹脂浸透性のある化粧材の裏面にガラス繊維を含む樹脂
浸透性のあるシート材を重ね合わせ、シート材の裏面に
熱伝導性が優れた金属の薄板を重ね合わせて接着し、シ
ート材及び化粧材の全部又は一部に樹脂が含浸固化され
ていることを特徴とする暖房ヒータ用表面仕上材。
2. A surface finishing material for a heater provided on a front side of a panel-type heating heater, wherein a resin-permeable sheet material containing glass fiber is superimposed on a back surface of a resin-permeable decorative material, A surface finishing material for a heating heater, characterized in that a metal thin plate having excellent thermal conductivity is superposed and adhered to the back surface of the material, and resin is impregnated and solidified in all or a part of the sheet material and the decorative material.
【請求項3】 シート材及び化粧材に含浸固化された樹
脂が、フェノール樹脂、エポキシ樹脂、ウレタン樹脂、
ユリア樹脂のいずれか1又は2以上の混合物であること
を特徴とする請求項1又は2に記載の暖房ヒータ用表面
仕上材。
3. The resin impregnated and solidified in the sheet material and the decorative material is a phenol resin, an epoxy resin, a urethane resin,
The surface finishing material for a heating heater according to claim 1 or 2, wherein the surface finishing material is a mixture of one or more of urea resins.
【請求項4】 化粧材が、突き板又は紙であることを特
徴とする請求項1ないし3のいずれか1項に記載の暖房
ヒータ用表面仕上材。
4. The surface finishing material for a heating heater according to claim 1, wherein the decorative material is a veneer or paper.
JP2000083137A 2000-03-24 2000-03-24 Surface finish material for heater Pending JP2001263699A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2000083137A JP2001263699A (en) 2000-03-24 2000-03-24 Surface finish material for heater

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2000083137A JP2001263699A (en) 2000-03-24 2000-03-24 Surface finish material for heater

Publications (1)

Publication Number Publication Date
JP2001263699A true JP2001263699A (en) 2001-09-26

Family

ID=18599826

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2000083137A Pending JP2001263699A (en) 2000-03-24 2000-03-24 Surface finish material for heater

Country Status (1)

Country Link
JP (1) JP2001263699A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2383295A (en) * 2001-12-19 2003-06-25 Michael Ghahari Repairable solid surface laminate

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2383295A (en) * 2001-12-19 2003-06-25 Michael Ghahari Repairable solid surface laminate

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