JPH01283141A - Decorative sheet - Google Patents
Decorative sheetInfo
- Publication number
- JPH01283141A JPH01283141A JP11289988A JP11289988A JPH01283141A JP H01283141 A JPH01283141 A JP H01283141A JP 11289988 A JP11289988 A JP 11289988A JP 11289988 A JP11289988 A JP 11289988A JP H01283141 A JPH01283141 A JP H01283141A
- Authority
- JP
- Japan
- Prior art keywords
- boiling
- resin
- impregnated
- paper
- increasing rate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000009835 boiling Methods 0.000 claims abstract description 14
- 239000000463 material Substances 0.000 claims abstract description 8
- 229920000877 Melamine resin Polymers 0.000 claims abstract description 6
- 229920000642 polymer Polymers 0.000 claims abstract description 4
- 238000011156 evaluation Methods 0.000 claims abstract description 3
- 238000000465 moulding Methods 0.000 claims description 9
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical class [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 8
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 3
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 claims description 3
- 239000011134 resol-type phenolic resin Substances 0.000 claims 1
- 239000000123 paper Substances 0.000 abstract description 13
- 239000005011 phenolic resin Substances 0.000 abstract description 12
- 238000005470 impregnation Methods 0.000 abstract description 5
- 150000002989 phenols Chemical class 0.000 abstract description 5
- 239000004640 Melamine resin Substances 0.000 abstract description 3
- 239000000835 fiber Substances 0.000 abstract description 3
- 238000010438 heat treatment Methods 0.000 abstract description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 2
- 239000004677 Nylon Substances 0.000 abstract description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 abstract description 2
- 229920002978 Vinylon Polymers 0.000 abstract description 2
- 239000004744 fabric Substances 0.000 abstract description 2
- 239000011521 glass Substances 0.000 abstract description 2
- 239000012784 inorganic fiber Substances 0.000 abstract description 2
- 239000004745 nonwoven fabric Substances 0.000 abstract description 2
- 229920001778 nylon Polymers 0.000 abstract description 2
- -1 polyoxyethylene Polymers 0.000 abstract description 2
- 229920002994 synthetic fiber Polymers 0.000 abstract description 2
- 239000012209 synthetic fiber Substances 0.000 abstract description 2
- 239000002657 fibrous material Substances 0.000 abstract 1
- 238000010030 laminating Methods 0.000 abstract 1
- 238000012360 testing method Methods 0.000 description 24
- 229920005989 resin Polymers 0.000 description 18
- 239000011347 resin Substances 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 5
- 238000005452 bending Methods 0.000 description 4
- 239000012792 core layer Substances 0.000 description 4
- 229920001568 phenolic resin Polymers 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 239000002655 kraft paper Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000032798 delamination Effects 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000007731 hot pressing Methods 0.000 description 2
- 239000011229 interlayer Substances 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229920003987 resole Polymers 0.000 description 2
- LMYRWZFENFIFIT-UHFFFAOYSA-N toluene-4-sulfonamide Chemical compound CC1=CC=C(S(N)(=O)=O)C=C1 LMYRWZFENFIFIT-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 241000287531 Psittacidae Species 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Abstract
Description
【発明の詳細な説明】
く技術分野〉
本発明は建築部材、家具部材等に使用される化粧板に関
するものである。DETAILED DESCRIPTION OF THE INVENTION Technical Field The present invention relates to decorative laminates used for building components, furniture components, and the like.
く従来技術〉
表面層がメラミン樹脂、コアー層がフェノール樹脂から
なる化粧&は表面性能に丁ぐれることがら各種の用途V
C利用されている。該化粧板ではコアー層に使用するフ
ェノール樹脂の樹脂流゛れを改喪する丸め変性が行われ
ている。これは樹脂流れが悪いものはコアー層の樹脂率
にムラが生じ成形時及びポストフォーミング加工時のパ
ンク、密)W不良による層間剥離あるいは成形品の反り
の本図になるためである。一方樹脂流れを改善するため
親水性変性剤等で変性したものでは耐水性、耐熱水性等
が劣り、中ツチ7等の水廻りの機器に使用され九場合、
木口より脹れるなどの問題が残されていた。Conventional technology〉 The surface layer is made of melamine resin and the core layer is made of phenolic resin.It has a variety of applications due to its excellent surface performance.
C. It is used. The decorative board is subjected to rounding modification to improve the resin flow of the phenolic resin used in the core layer. This is because if the resin flow is poor, the resin ratio in the core layer will be uneven, resulting in punctures during molding and post-forming, interlayer peeling due to W defects, or warping of the molded product. On the other hand, those modified with hydrophilic modifiers to improve resin flow have inferior water resistance and hot water resistance, and are used in water-related equipment such as Nakatsuchi 7.
Problems such as swelling from the end remained.
〈発明の目的〉
本発明は上記の事情に鑑み検討された結果なされたもの
で、樹m*れが良好なフェノール樹脂により均一に成形
されすぐれた耐水性、耐熱性のコアー層を有する化粧板
を提供するものである0〈発明の開示〉
本発明の懺旨は前記の通りであり、以下詳細に説明する
。本発明に係るポリオキシエチレンポリオキシプロピレ
ンブロック重合体はプロピレンオキシドにエチレンオキ
シドを附加したもので、工テレ/オキシドが組成比5〜
5096で分子量が3000以下のものが使用される。<Purpose of the Invention> The present invention was made as a result of studies in view of the above circumstances, and provides a decorative board having a core layer uniformly molded from a phenolic resin with good mold resistance and having excellent water resistance and heat resistance. <Disclosure of the Invention> The gist of the present invention is as described above, and will be explained in detail below. The polyoxyethylene polyoxypropylene block polymer according to the present invention is made by adding ethylene oxide to propylene oxide, and the composition ratio of polyoxyethylene/oxide is 5 to 5.
5096 with a molecular weight of 3000 or less.
分子量が3000以上のものはクラフト紙等の基材への
浸透が損われる丸め好1しくない。またエチレンオキシ
ドの組成比が50%以上であると化粧板の耐水性が低下
ならびに含浸時の発泡などかめ9好ましくない。Those with a molecular weight of 3,000 or more are not suitable for rounding as they impair penetration into base materials such as kraft paper. Furthermore, if the composition ratio of ethylene oxide is 50% or more, the water resistance of the decorative board decreases and foaming occurs during impregnation, which is undesirable.
フェノールm 脂Fiフェノールに対するホルムアルデ
ヒドのモル比が0.8〜2.0のレゾールタイプのもの
、好ましくはゲルタイムが1〜5m1n/ンブロツク嵐
合体の添加率は樹脂分に対し2〜30チが適合する。2
%以下では変性効果が得られず、30%以上では耐熱水
性、耐熱性が低下し好ましくない。Phenol (m) Resol type with a molar ratio of formaldehyde to phenol of 0.8 to 2.0, preferably a gel time of 1 to 5 m1n/block storm combination addition rate of 2 to 30 m to resin content. . 2
If it is less than 30%, no modification effect will be obtained, and if it is more than 30%, hot water resistance and heat resistance will decrease, which is not preferable.
本発明になる化粧材に係る含浸用の基材にはαセルロー
ス、リンター等の天然繊維単独もしくは該天然繊維にビ
ニロン、ナイロン等の合成繊維、ガラス等の無機繊維等
が混入され九繊維材料から作られた多孔質な紙、不織布
、布等が使用される。The base material for impregnation of the decorative material of the present invention is made from natural fibers such as alpha cellulose and linters alone, or mixed with synthetic fibers such as vinylon and nylon, inorganic fibers such as glass, etc. Porous paper, non-woven fabric, cloth, etc. are used.
上記のように変性されたフェノール樹脂は基材重量に対
し40〜70%含浸処理されて成形用シートに仕上げら
れる。含浸処理率が40%以下では成形性に欠け、層間
剥離の原因になり、70チ以上では樹脂の流出ロスが激
しく好ましくない。The phenol resin modified as described above is impregnated with 40 to 70% of the weight of the base material, and is finished into a sheet for molding. If the impregnation rate is less than 40%, the moldability will be poor and it will cause delamination, and if it is more than 70%, the loss of resin flowing out will be severe, which is not preferable.
成形用シートは複数枚が積層されるか、あるいはその上
にメラミン樹脂含浸紙が重ねられて熱圧成形され積層板
又は化粧板に成形される。A plurality of molding sheets are laminated, or melamine resin-impregnated paper is layered thereon and hot-press molded to form a laminate or decorative board.
次に実施例、比較例により説明する。Next, examples and comparative examples will be explained.
実施例1及び実施例2
フェノールに対するホルマリンのモル比1.5のレゾー
ルタイプの未変性フェノール樹脂に対し樹脂弁当920
%、プルロニックL31(旭電化製ポリオキシエチレン
ポリオキシプロピレンブロック重合体 平均分子111
00、エチレンオキシド組成10%)を添加した変性フ
ェノール樹脂(11及びプルロニックL 62 (1m
l上、平均分子シ2000、エチレンオキシド組成20
%)を酢加した変性フェノール樹脂(2)を調製した。Examples 1 and 2 Resin bento 920 for resol type unmodified phenolic resin with a molar ratio of formalin to phenol of 1.5
%, Pluronic L31 (polyoxyethylene polyoxypropylene block polymer manufactured by Asahi Denka, average molecular weight 111
00, modified phenolic resin (11 and Pluronic L 62 (1 m
l, average molecular weight 2000, ethylene oxide composition 20
A modified phenol resin (2) to which %) was added with acetic acid was prepared.
これをクラフト紙に樹脂率50チ含浸し、成形用の含浸
紙(4)及びCB)t−得た。該含浸紙囚及び@を各8
枚重ね熱圧成形して積層板(イ)及び(ロ)を作成した
。また該含浸紙囚及び■各3枚の上に印刷紙にメラミン
樹1kを含浸した化粧mt重ね熱圧成形して厚さ0.8
鵡の化粧板(Q及び0を作成した。This was impregnated into kraft paper at a resin rate of 50 g to obtain impregnated paper (4) and CB) for molding. 8 each of the impregnated paper and @
Laminated plates (a) and (b) were created by stacking them and hot-pressing them. In addition, on top of each of the impregnated paper sheets and (1) 3 sheets each, printed paper impregnated with 1k of melamine wood was layered and hot-press molded to a thickness of 0.8.
I created a decorative board for a parrot (Q and 0).
該積層板(イ)及び(口>を成形する際の樹脂流動性、
該化粧板(Q及び0の煮沸重量増加率、煮沸厚さ増加率
、耐熱性ならびに曲げ成形性は表の通りでろつIt−。Resin fluidity when molding the laminate (a) and (mouth);
The boiling weight increase rate, boiling thickness increase rate, heat resistance, and bending formability of the decorative boards (Q and 0) are as shown in the table.
比較例1及び2
実施例1及び2で使用した該未変性フェノール樹脂及び
該未変性フェノール樹脂に対してパラトルエンスルホン
アミド(PTSA)を20%m加した食性フェノール樹
脂を実施例で使用したものと同一のクラフト紙に樹脂率
50チ含浸処理して含改紙(ト)及び■)を得た。該含
浸紙■及び山)を各8枚電ね熱圧成形して積層板(/→
及びに)を作成した。Comparative Examples 1 and 2 The unmodified phenol resin used in Examples 1 and 2 and the edible phenol resin in which 20% of paratoluenesulfonamide (PTSA) was added to the unmodified phenol resin were used in the examples. The same kraft paper was impregnated with resin at a rate of 50% to obtain modified paper (G) and (2). 8 sheets each of the impregnated paper (■ and pile) were formed by thermo-pressure molding to form a laminate (/→
and ) were created.
また該含浸紙(ト)及びω)各3枚の上に、実施例と同
一の化粧紙を重ね熱圧成形して厚さ0,8顕の化粧板Ω
及びG()を作成した。In addition, the same decorative paper as in the example was layered on three sheets each of the impregnated paper (G) and ω), and hot-press molded to form a decorative board with a thickness of 0.8 Ω.
and G() were created.
該積層板e′1及びに)を成形する際の樹脂流動性及び
成形時のパンクの有無、該化粧板(Q及び0の煮り%重
量増加率、煮沸厚さ増加率等の特性値は表の通りであっ
た。Characteristic values such as the resin fluidity and the presence or absence of punctures during molding of the laminates e'1 and 2), the boiling % weight increase rate and the boiling thickness increase rate of the decorative laminates (Q and 0) are It was as shown in the table.
表
評価法
(1)樹脂流動性
含浸紙より一定の形状(120X120w角)の試片を
必快枚数切り抜き8枚重ね140℃。Table evaluation method (1) Cut out as many specimens of a certain shape (120x120w square) as possible from resin fluidity-impregnated paper and stack 8 sheets at 140°C.
100kg/iで15分間熱圧して積層板を成形する際
の該試験片の重量及び流出樹脂を除いた積層板の重量を
求め次式より樹脂流動性を算出する。The weight of the test piece when molding a laminate by hot pressing at 100 kg/i for 15 minutes and the weight of the laminate excluding the flowed resin are determined, and the resin fluidity is calculated from the following formula.
試験片重量−積層機重量
樹脂流動性(慢)= X
100試験片虱童
(2)煮梯重輩増加率及び煮沸厚さ増加率の恒温器中に
24±1時間靜置したのち、デシケータ−中で常温まで
放冷する0
(ロ)つぎに、試験片の憲さを1mg まではかり、厚
さを外側マイクロメータで4周縁のそれぞれ中央部のほ
ぼ5困内側の測定点を0.01s+sまではかる。Test piece weight - Layer weight Resin fluidity (slow) = X
100 test pieces (2) After being placed in a thermostat with a boiling layer thickness increase rate and a boiling thickness increase rate for 24 ± 1 hours, the pieces were allowed to cool to room temperature in a desiccator (B) Next, Weigh the strength of the test piece to the nearest 1 mg, and measure the thickness to the nearest 0.01 s + s at measurement points approximately 500 mm inside the center of each of the four peripheries using an outside micrometer.
e→ ビーカーの中に蒸留水を入れて、これを適当な熱
源で加熱して沸騰させてから、その中に試験片を完全に
浸す0試験片と試験片、または試験片と容器が密着しな
いようにする。e→ Put distilled water in a beaker, heat it with an appropriate heat source, bring it to a boil, and then completely immerse the test piece in it. 0 The test piece and the test piece or the test piece and the container do not come into close contact. do it like this.
2時間±5分煮沸してから試験片を取り出し、室温(2
0±5℃)に保持し丸蓋留水の中で約15分間冷却する
。After boiling for 2 hours ± 5 minutes, take out the test piece and leave it at room temperature (2
0±5°C) and cooled in a round lid of distilled water for about 15 minutes.
に)水から取り出し、試験片に付着している水分を清浄
なガーゼまたはろ紙でぬぐいとる。b) Remove from the water and wipe off any moisture adhering to the test piece with clean gauze or filter paper.
1分以内に試験片を1mg’まではかる7、4箇所の厚
さを前と同じ測定点において0.01關までは±1時間
静置したのち、これを取り出してデシケータ−中で常温
になるまで放冷する〇(へ)試験片の層間はく離がある
かどつかを肉眼で調べる。Measure the test piece to 1 mg' within 1 minute 7. Measure the thickness of the test piece at the same measurement point as before to 0.01 ± 1 hour. Take it out and let it come to room temperature in a desiccator. Leave to cool until 〇(f) Visually inspect the test piece to see if there is any interlayer delamination.
試料の重さ増加率W(@および厚さ増加率D(%)は、
試験片ごとにつぎの式により算出したそれぞれ3個の平
均値をもって表わす。The weight increase rate W (@ and the thickness increase rate D (%) of the sample are:
Each test piece is expressed as the average value of three values calculated using the following formula.
Wl −Wl Dt−D。Wl-Wl Dt-D.
ここに W:試験片個々の重さ増加率(%)D:試験片
個々の厚さ増加率(働
Wo;試験前の試験片の重さ(g)
Wl:試験後の試験片の重さ(g)
Do=試験前の試験片の厚さ(闘)
Dl:試験後の試験片の厚さ(acg+)(3)加熱時
のパンク温度
化粧板の表向に所定の温度で浴融する示温塗料を塗布し
たのち遠赤外線ヒーターにて加熱してパンク時の表面温
度を測定した。Here, W: Weight increase rate of each test piece (%) D: Thickness increase rate of each test piece (Wo: Weight of test piece before test (g) Wl: Weight of test piece after test (g) Do = Thickness of the test piece before the test (T) Dl: Thickness of the test piece after the test (ACG+) (3) Puncture temperature during heating Melt the surface of the decorative board in a bath at a predetermined temperature After applying a temperature-indicating paint, it was heated with a far-infrared heater and the surface temperature at the time of puncture was measured.
(4) 曲げ成形性
JISK6902の方法による
第1図の曲げ成形装置を使用し、裏面に測温クレヨンで
紛を数条引き、各加熱温度に加熱し九試験片を装置に表
面側がメス型に接するように装j#シ、1分問屋にはさ
んだiま放冷して取り出し、表面にフクレ、ヒビ及びハ
クリがないか、型のとおり成形憾れているかどうかを肉
眼で調べる。(4) Bending formability Using the bending device shown in Figure 1 according to the JIS K6902 method, draw several lines of powder on the back side with a thermometer crayon and heat to each heating temperature. Place them so that they touch each other, leave them in a wholesaler for 1 minute, let them cool, then take them out and visually inspect the surface to see if there are any blisters, cracks, or peeling, and if they are molded according to the mold.
(発明の効果〉
本発明になる積層板及び化粧板は無質性のフェノール樹
脂おるいは従来の方法による変性フェノール樹脂が使用
され良ものに比べ樹脂流動性、煮沸時のI量増加率、厚
さ増加率、耐熱性ならびに曲は成形性が著しく改善され
、これまでに比べ高品質のものが得られる。更にこれら
の特性を得るために樹脂含浸率を高く維持する必費があ
りたが、本発明になる積層板及び化粧板はこのような必
戦かなくなり低樹脂率化が可能となるため低コスト化が
はかれる。(Effects of the Invention) The laminates and decorative laminates of the present invention use amorphous phenolic resin or modified phenolic resin by conventional methods, and have better resin fluidity, increased rate of increase in I amount during boiling, Thickness increase rate, heat resistance, and moldability have been significantly improved, and higher quality products can be obtained than before.Furthermore, in order to obtain these characteristics, it was necessary to maintain a high resin impregnation rate. The laminates and decorative laminates of the present invention do not require such a battle and can be made with a low resin content, resulting in lower costs.
第1図は曲げ成型装置(1)の斜視図である。
1・・・曲けgmagt
2・・・メス型 3・・・オス屋4・・・スプリ
ング
特許出願人 アイカニ業株式会社FIG. 1 is a perspective view of a bending and forming device (1). 1...Bent gmagt 2...Female type 3...Male 4...Spring patent applicant Aikani Gyo Co., Ltd.
Claims (1)
チレンポリオキシプロピレンブロック重合体が混入され
た変性フェノール樹脂を多孔質な基材に含浸されてなる
成形用シートの上にメラミン樹脂含浸紙が重ねられ積層
成形されたものであって、JISK6902の評価法に
よる煮沸重量増加率が9.5〜8.5%、煮沸厚さ増加
率が10〜12%であって、加熱時のパンク温度が20
0℃以上であることを特徴とする化粧板(1) A melamine resin-impregnated paper is laminated on a molding sheet made of a porous base material impregnated with a modified phenolic resin, which is a resol type phenolic resin mixed with a polyoxyethylene polyoxypropylene block polymer. The molded product has a boiling weight increase rate of 9.5 to 8.5%, a boiling thickness increase rate of 10 to 12%, and a puncture temperature of 20% when heated, according to the JIS K6902 evaluation method.
Decorative board characterized by a temperature of 0°C or higher
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11289988A JPH0615223B2 (en) | 1988-05-10 | 1988-05-10 | Veneer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11289988A JPH0615223B2 (en) | 1988-05-10 | 1988-05-10 | Veneer |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01283141A true JPH01283141A (en) | 1989-11-14 |
JPH0615223B2 JPH0615223B2 (en) | 1994-03-02 |
Family
ID=14598285
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11289988A Expired - Lifetime JPH0615223B2 (en) | 1988-05-10 | 1988-05-10 | Veneer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0615223B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5436031A (en) * | 1991-06-24 | 1995-07-25 | Isovolta Osterreichische Isolierstoffwerke Aktiengesellschaft | Method for impregnating a heated, flat, fibrous substrate with synthetic resin |
-
1988
- 1988-05-10 JP JP11289988A patent/JPH0615223B2/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5436031A (en) * | 1991-06-24 | 1995-07-25 | Isovolta Osterreichische Isolierstoffwerke Aktiengesellschaft | Method for impregnating a heated, flat, fibrous substrate with synthetic resin |
Also Published As
Publication number | Publication date |
---|---|
JPH0615223B2 (en) | 1994-03-02 |
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