JPH06272193A - Sheet material - Google Patents

Sheet material

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Publication number
JPH06272193A
JPH06272193A JP5718593A JP5718593A JPH06272193A JP H06272193 A JPH06272193 A JP H06272193A JP 5718593 A JP5718593 A JP 5718593A JP 5718593 A JP5718593 A JP 5718593A JP H06272193 A JPH06272193 A JP H06272193A
Authority
JP
Japan
Prior art keywords
sheet
sol
polyvinyl chloride
sheet material
surface smoothness
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
JP5718593A
Other languages
Japanese (ja)
Inventor
Kiyoshi Shibuya
潔司 澁谷
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Paper Mills Ltd
Original Assignee
Mitsubishi Paper Mills 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 Mitsubishi Paper Mills Ltd filed Critical Mitsubishi Paper Mills Ltd
Priority to JP5718593A priority Critical patent/JPH06272193A/en
Publication of JPH06272193A publication Critical patent/JPH06272193A/en
Pending legal-status Critical Current

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  • Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Paper (AREA)

Abstract

PURPOSE:To obtain a sheet material excellent in surface smoothness and interlayer peeling strength and further excellent in sol non-strike through property and sol-adhering property, when processed with the polyvinyl chloride sol. CONSTITUTION:The characteristic of this sheet material mainly formed of glass fibers and pulp comprises that a cation-modified aromatic polyurethane resin is impregnated into the sheet in an amount of 5-20wt.% based on thw weight of the sheet. The sheet material is excellent in surface smoothness and interlayer peeling strength, after coated with a polyvinyl chloride sol, and further excellent in sol non-strike through property and sol-adhering property.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は,表面平滑性および層間
剥離強度に優れ,かつポリ塩化ビニルゾルとの加工時に
おける,ゾルの裏抜け防止性およびゾルとの接着性に優
れたシート材料に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a sheet material which is excellent in surface smoothness and delamination strength, and is excellent in sol strike-through prevention and adhesion to a sol during processing with a polyvinyl chloride sol. Is.

【0002】[0002]

【従来の技術】近年,建築内装材料として発泡塩ビクッ
ションフロア(以下クッションフロア)が広く用いられ
てきているが,一般的にこれらのクッションフロアは,
寸法安定性および強度付与の観点から,ガラス繊維およ
びパルプを主としたシート材料と組み合わせて使用され
ている。このクッションフロアの柄として,以前は絵柄
もしくは幾何学模様柄が使用されていたが,生活様式の
欧米指向化等によりフローリング調の木目柄が急速に普
及してきており,表面平滑性および層間剥離強度等に対
する要求品質が厳しくなる傾向にある。
2. Description of the Related Art In recent years, foamed PVC cushion floors (hereinafter referred to as cushion floors) have been widely used as building interior materials. Generally, these cushion floors are
From the viewpoint of dimensional stability and imparting strength, it is used in combination with sheet materials mainly composed of glass fiber and pulp. As a pattern for this cushion floor, a pattern or a geometric pattern was used before, but the flooring-like wood grain pattern has been rapidly spread due to the Western-oriented lifestyle, and the surface smoothness and delamination strength are increasing. There is a tendency that the required quality for the above becomes strict.

【0003】例えば,特開昭55−16901号公報で
は,塩化ビニル系樹脂等の熱可塑性樹脂粉末および反応
型樹脂等を,特定割合でガラス繊維等に含有させ,シー
ト化する方法が提案されているが,熱可塑性樹脂粉末の
付着量いわゆる歩留まりには限界があり,また樹脂粉末
間に生じる空隙への塩ビゾルの浸透等により,クッショ
ンフロア全体として塩ビゾルの浸透は不均一となり,表
面平滑性は不十分なものである。
For example, Japanese Patent Laid-Open No. 55-16901 proposes a method in which a thermoplastic resin powder such as a vinyl chloride resin and a reactive resin are contained in glass fibers at a specific ratio to form a sheet. However, the amount of adhesion of the thermoplastic resin powder, the so-called yield, is limited, and due to the permeation of PVC sol into the voids between the resin powder, the permeation of PVC sol becomes uneven throughout the cushion floor, and the surface smoothness is Is inadequate.

【0004】また,特開昭57−106772号公報で
は,ガラス繊維など無機質繊維からなる多孔質の不織布
基材に対して,ポリフルオロアルキル基含有化合物を添
着させる方法が提案されているが,やはり化合物の添着
量には限界があり,また塩ビゾルとの接着性には優れる
ものの,多孔質体空隙への塩ビゾルの浸透等により,ク
ッションフロア全体として塩ビゾルの浸透性は不均一と
なり,表面平滑性は不十分なものである。
Further, Japanese Patent Application Laid-Open No. 57-106772 proposes a method of attaching a polyfluoroalkyl group-containing compound to a porous non-woven fabric substrate made of inorganic fibers such as glass fibers. Although the amount of compound adhering is limited and the adhesiveness with PVC sol is excellent, due to the penetration of PVC sol into the voids of the porous body, the permeability of PVC sol becomes non-uniform on the entire cushion floor, and The smoothness is insufficient.

【0005】また,特開平01−164913号公報で
は,特定の平均繊維径および平均繊維長のガラス繊維を
主体とする中心層の表面に,細く,短いガラス繊維を主
体とする表面層を設けることが提案されているが,ガラ
ス繊維のみを主体とするため塩ビゾルの浸透量は多く,
また中心層と表面層の層間剥離強度は不十分なものであ
る。
In Japanese Patent Laid-Open No. 01-164913, a surface layer mainly composed of thin and short glass fibers is provided on the surface of a central layer composed mainly of glass fibers having a specific average fiber diameter and average fiber length. However, since only glass fiber is the main component, the permeation amount of PVC sol is large,
Further, the delamination strength between the central layer and the surface layer is insufficient.

【0006】[0006]

【発明が解決しようとする課題】建築内装材料として使
用されるクッションフロアは,寸法安定性および強度付
与の観点から,ガラス繊維およびパルプを主としたシー
ト材料と組み合わせて使用されているが,近年表面平滑
性および層間剥離強度等の要求品質が高まり,従来のシ
ート材料では,かかる品質に対応することは難しいこと
が明らかになった。
The cushion floor used as a building interior material is used in combination with a sheet material mainly composed of glass fiber and pulp from the viewpoint of dimensional stability and imparting strength. It has become clear that it is difficult to meet such qualities with conventional sheet materials, as the required qualities such as surface smoothness and delamination strength have increased.

【0007】[0007]

【課題を解決するための手段】本発明は,主としてガラ
ス繊維およびパルプから形成されるシートにおいて,該
シートの2次加工用バインダーとしてカチオン変性芳香
族ポリウレタン樹脂が使用され,前記カチオン変性芳香
族ポリウレタン樹脂の含浸量が,シート重量に対して5
から20重量%であることを特徴とするものである。
According to the present invention, in a sheet formed mainly of glass fiber and pulp, a cation-modified aromatic polyurethane resin is used as a binder for secondary processing of the sheet. Resin impregnation amount is 5 relative to the sheet weight
To 20% by weight.

【0008】本発明で用いられるカチオン変性芳香族ポ
リウレタン樹脂としては,例えば,アクリル・ウレタン
共重合体,ポリビニル・ウレタン共重合体,ポリエーテ
ル・ウレタン共重合体,ポリエステル・ウレタン共重合
体等が挙げられ,1次バインダー含浸したシートに対し
て,含浸量が5重量%以下では皮膜形成によるシートマ
スキング効果が不十分であり,表面平滑性およびポリ塩
化ビニルゾルの裏抜け防止性の問題があり,20重量%
以上ではポリウレタン樹脂の含浸工程に於ける2次加工
性およびコストの点で問題がある。
Examples of the cation-modified aromatic polyurethane resin used in the present invention include acrylic / urethane copolymer, polyvinyl / urethane copolymer, polyether / urethane copolymer, polyester / urethane copolymer and the like. When the impregnated amount is 5% by weight or less, the sheet masking effect by film formation is insufficient for the sheet impregnated with the primary binder, and there are problems of surface smoothness and strike-through prevention of polyvinyl chloride sol. weight%
Above, there is a problem in secondary processability and cost in the impregnation process of polyurethane resin.

【0009】また,ポリウレタン樹脂のイオン性は,カ
チオン性であることがシート中のガラス繊維およびパル
プへの吸着または接着性の点で好ましく,アニオン性で
はシートへの定着性が劣り,シートの層間剥離強度の点
で問題がある。
Further, the ionic property of the polyurethane resin is preferably cationic in terms of adsorption or adhesion to the glass fiber and pulp in the sheet, and when anionic, the fixing property to the sheet is poor and the interlayer of the sheet is poor. There is a problem in peel strength.

【0010】[0010]

【実施例】次に実施例を用い,更に詳細に本発明を説明
する。なお以下に示す部および%はいずれも重量基準で
ある。
EXAMPLES Next, the present invention will be described in more detail with reference to examples. All parts and% shown below are based on weight.

【0011】実施例1 (1)2次加工用原布の作成 繊維径9μm,繊維長6mmのチョップドストランドガ
ラス16gを水4.5l中に投入し,更に0.2%ポリ
アクリルアマイド水溶液0.5lを加えて,往復回転式
アジターにて15分間攪はんし,濃度0.32%のスラ
リーを得た。次に,濾水度500mlのNBKP叩解
パルプ12.8gおよびPVA繊維3.2gを水4.5
lに加え,高速ミキサーにて5分間攪はんし,更に0.
2%ポリアクリルアマイド水溶液0.5lを加えて濃度
0.32%のスラリーを得た。
Example 1 (1) Preparation of secondary processing base fabric 16 g of chopped strand glass having a fiber diameter of 9 μm and a fiber length of 6 mm was put into 4.5 liters of water, and 0.2% polyacrylic amide aqueous solution was further added. 5 l was added and the mixture was stirred with a reciprocating rotary agitator for 15 minutes to obtain a slurry having a concentration of 0.32%. Next, 12.8 g of NBKP beaten pulp having a freeness of 500 ml and 3.2 g of PVA fiber were mixed with 4.5 parts of water.
In addition to 1, the mixture was stirred with a high-speed mixer for 5 minutes, and further stirred to 0.
0.5 l of a 2% polyacrylic amide aqueous solution was added to obtain a slurry having a concentration of 0.32%.

【0012】スラリーおよびを各々0.5lづつ角
形手抄き箱に投入し,更に10倍濃度まで希釈した後脱
水し,ウェットシートを得た。出来たウェットシートは
線圧10kg/cmのシートプレスマシンにてプレス
後,ヤンキー型乾燥機で乾燥して,目付け80g/m2
の2次加工用原布を得た。
0.5 l of each of the slurry and each was put into a square handmade box, further diluted to 10 times the concentration, and then dehydrated to obtain a wet sheet. The resulting wet sheet is pressed by a sheet press machine with a linear pressure of 10 kg / cm, and then dried by a Yankee dryer to give a basis weight of 80 g / m 2.
To obtain a secondary processing raw fabric.

【0013】(2)2次加工用バインダーの作成 下記配合で示される2次加工用バインダーを上記2次加
工用原布に対して5g/m2 含浸し,目付け85g/m
2 のシートを得た。 日華化学工業製 ネオセロ10A(40%液) 50部 水 200部
(2) Preparation of Binder for Secondary Processing 5 g / m 2 of the binder for secondary processing represented by the following composition was impregnated with the base fabric for secondary processing to give a basis weight of 85 g / m 2.
I got 2 sheets. NISSA CHEMICAL INDUSTRIES Neocello 10A (40% liquid) 50 parts Water 200 parts

【0014】(3)ポリ塩化ビニルゾルの作成 下記配合で示される混合物を,ホバート型ミキサーにて
40分間混練し,粘度6000m.Pa.sのポリ塩化
ビニルゾルを得た。 ポリ塩化ビニルペースト(日本ゼオン製ゼオン126) 100部 可塑剤(花王製ビニサイザー80) 60部 Ba−Zn系安定剤 1部 酸化亜鉛 10部 炭酸カルシウム 30部 アゾジカルボンアミド 4部
(3) Preparation of polyvinyl chloride sol A mixture represented by the following composition was kneaded with a Hobart type mixer for 40 minutes to give a viscosity of 6000 m. Pa. A polyvinyl chloride sol of s was obtained. Polyvinyl chloride paste (ZEON 126 manufactured by Nippon Zeon) 100 parts Plasticizer (Vinizer 80 manufactured by Kao) 60 parts Ba-Zn stabilizer 1 part Zinc oxide 10 parts Calcium carbonate 30 parts Azodicarbonamide 4 parts

【0015】2次加工後のシートに対して,前記ポリ塩
化ビニルゾルを,クリアランス0.4mmのバーコータ
ーにて塗布し,200℃,30秒間電気炉の中にてゲル
化後目付け465g/m2 のシートを得た。この時ポリ
塩化ビニルゾルの塗布量は380g/m2 であった。出
来上がったシートは,表面平滑性および層間剥離強度に
優れ,またポリ塩化ビニルゾルのシートへの浸透量も少
なく,ゾルの裏抜けも無かった。評価結果は表1に示
す。
The polyvinyl chloride sol was applied to the sheet after secondary processing with a bar coater having a clearance of 0.4 mm, and the fabric weight after gelling was 465 g / m 2 in an electric furnace at 200 ° C. for 30 seconds. Got a sheet of. At this time, the coating amount of polyvinyl chloride sol was 380 g / m 2 . The finished sheet had excellent surface smoothness and delamination strength, the amount of permeation of polyvinyl chloride sol into the sheet was small, and there was no strike-through of the sol. The evaluation results are shown in Table 1.

【0016】実施例2 実施例1と同様にして得られた,目付け80g/m2
2次加工用原布に対して,下記配合で示される2次加工
用バインダーを11g/m2 含浸し,目付け91g/m
2 のシートを得た。 日華化学工業製 ネオセロ10A(40%液) 120部 水 200部 前期シートに対して,実施例1と同様にポリ塩化ビニル
ゾルを塗布し,目付け471g/m2 のシートを得た。
出来上がったシートは,表面平滑性および層間剥離強度
に極めて優れ,またポリ塩化ビニルゾルのシートへの浸
透量も少なく,ゾルの裏抜けも無かった。評価結果は表
1に示す。
Example 2 A secondary processing raw fabric having a basis weight of 80 g / m 2 obtained in the same manner as in Example 1 was impregnated with a secondary processing binder represented by the following composition in an amount of 11 g / m 2. , Basis weight 91g / m
I got 2 sheets. NEO-CELLO 10A (40% liquid) manufactured by Nichika Chemical Co., Ltd. 120 parts Water 200 parts Polyvinyl chloride sol was applied to the previous sheet in the same manner as in Example 1 to obtain a sheet having a basis weight of 471 g / m 2 .
The finished sheet was extremely excellent in surface smoothness and delamination strength, the amount of permeation of polyvinyl chloride sol into the sheet was small, and there was no strike-through of the sol. The evaluation results are shown in Table 1.

【0017】比較例1 実施例1と同様にして得られた,目付け80g/m2
2次加工用原布に対して,下記配合で示される2次加工
用バインダーを2g/m2 含浸し,目付け82g/m2
のシートを得た。 日華化学工業製 ネオセロ10A(40%液) 20部 水 200部 前期シートに対して,実施例1と同様にポリ塩化ビニル
ゾルを塗布し,目付け462g/m2 のシートを得た。
出来上がったシートは,微細な凹凸が発生し表面平滑性
に劣り,層間剥離強度も小さく,またポリ塩化ビニルゾ
ルのシートへの浸透量も多く,部分的にゾルの裏抜けが
認められた。これはポリウレタン樹脂の含浸量が少な
く,シート全体に対するポリウレタン樹脂のマスキング
効果が不十分な為と考えられる。評価結果は表1に示
す。
Comparative Example 1 A secondary processing raw fabric having a basis weight of 80 g / m 2 obtained in the same manner as in Example 1 was impregnated with 2 g / m 2 of a secondary processing binder having the following composition. , Basis weight 82 g / m 2
Got a sheet of. NEO-CELLO 10A (40% solution) 20 parts water 200 parts manufactured by Nichika Kagaku Kogyo Co., Ltd. was coated with polyvinyl chloride sol in the same manner as in Example 1 to obtain a sheet having a basis weight of 462 g / m 2 .
The finished sheet had fine irregularities, poor surface smoothness, low interlaminar peel strength, and a large amount of polyvinyl chloride sol permeation into the sheet, indicating partial strike-through of the sol. This is probably because the amount of impregnated polyurethane resin is small and the masking effect of polyurethane resin on the entire sheet is insufficient. The evaluation results are shown in Table 1.

【0018】比較例2 実施例1と同様にして得られた,目付け80g/m2
2次加工用原布に対して,下記配合で示される2次加工
用バインダーを6g/m2 含浸し,目付け86g/m2
のシートを得た。 大日本インキ化学製 ディクナールNP99(40%液) 50部 水 200部 前期シートに対して,実施例1と同様にポリ塩化ビニル
ゾルを塗布し,目付け466g/m2 のシートを得た。
出来上がったシートは,表面に微小な凹凸が僅かに認め
られ,ゾル浸透量は小さいものの,層間剥離強度は小さ
かった。これはポリウレタン樹脂のイオン性がアニオン
性である為,シートに対する樹脂定着性のバラツキによ
るマスキング効果の不均一が生じ,またシート配合中の
パルプへ対する吸着および接着力が小さい為と考えられ
る。評価結果は表1に示す。
Comparative Example 2 A secondary processing raw fabric having a basis weight of 80 g / m 2 obtained in the same manner as in Example 1 was impregnated with a secondary processing binder having the following composition in an amount of 6 g / m 2. , Basis weight 86 g / m 2
Got a sheet of. Dainippon Ink and Chemicals DKNAL NP99 (40% liquid) 50 parts Water 200 parts Polyvinyl chloride sol was applied to the previous sheet in the same manner as in Example 1 to obtain a sheet having a basis weight of 466 g / m 2 .
The resulting sheet had slight irregularities on the surface, and although the amount of sol penetration was small, the delamination strength was low. It is considered that this is because the ionicity of the polyurethane resin is anionic, resulting in nonuniformity of the masking effect due to variations in resin fixing property to the sheet, and small adsorption and adhesive force to pulp during sheet formulation. The evaluation results are shown in Table 1.

【0019】比較例3 実施例1と同様にして得られた,目付け80g/m2
2次加工用原布に,直接ポリ塩化ビニルゾルを塗布し,
目付け460g/m2 のシートを得た。出来上がったシ
ートは,大きな凹凸が発生し表面平滑性に劣り,層間剥
離強度も小さく,またポリ塩化ビニルゾルのシートへの
浸透量も多く,全面的にゾルの裏抜けが認められた。こ
れはガラス繊維およびパルプのみの配合では,シートの
目詰め効果および層間強度が不十分である為と考えられ
る。評価結果は表1に示す。
Comparative Example 3 Polyvinyl chloride sol was directly applied to a base fabric for secondary processing having a basis weight of 80 g / m 2 obtained in the same manner as in Example 1,
A sheet having a basis weight of 460 g / m 2 was obtained. The resulting sheet had large irregularities, poor surface smoothness, low interlaminar peel strength, and a large amount of permeation of polyvinyl chloride sol into the sheet. This is considered to be because the sheet filling effect and the interlaminar strength are insufficient with only glass fiber and pulp. The evaluation results are shown in Table 1.

【0020】[0020]

【表1】 [Table 1]

【0021】表中の符号の意味は以下の通りである。 表面平滑性○ 目視判定にて,表面に凹凸が無く平滑な
面である 表面平滑性△ 目視判定にて,表面に微小な凹凸が僅か
に確認される 表面平滑性× 目視判定にて,表面に大きな凹凸が確認
される ゾル裏抜け○ 目視判定にて,表面に塗工したゾルが裏
面まで浸透しない ゾル裏抜け△ 目視判定にて,表面に塗工したゾルが僅
かに裏面まで浸透する ゾル裏抜け× 目視判定にて,表面に塗工したゾルが裏
面まで浸透する
The meanings of the symbols in the table are as follows. Surface smoothness ○ It is a smooth surface with no unevenness by visual judgment. Surface smoothness △ Microscopic unevenness is slightly confirmed on the surface by visual judgment. Surface smoothness × Visually determined by visual judgment. Large unevenness is confirmed.Sol back penetration ○ By visual judgment, the sol coated on the front surface does not penetrate to the back surface.Sol back penetration △ By visual judgment, the sol coated on the front surface penetrates slightly to the back surface. Omission x By visual judgment, the sol coated on the surface penetrates to the back surface

【0022】ゾル浸透量は,ポリ塩化ビニルゾルの塗布
重量およびゲル化後の塗布厚さより算出した。また剥離
強度は,ポリ塩化ビニルゾルをゲル化後,シート表面と
塩ビ層の間の層間強度を,テンシロン型万能試験機を用
い,JIS−K6854に準じて180度剥離にて測定
した。
The sol permeation amount was calculated from the coating weight of the polyvinyl chloride sol and the coating thickness after gelation. The peel strength was measured by gelling the polyvinyl chloride sol, and then measuring the interlayer strength between the sheet surface and the vinyl chloride layer by 180 degree peeling according to JIS-K6854 using a Tensilon type universal testing machine.

【0023】[0023]

【発明の効果】以上詳述したように,本発明のシート材
料によれば,表1の結果より明かなように,発泡塩ビク
ッションフロアの基材として使用された場合に,表面平
滑性および層間剥離強度に優れ,かつポリ塩化ビニルゾ
ルの裏抜け防止性およびゾルとの接着性に優れたシート
材料を得ることが出来る。
As described in detail above, according to the sheet material of the present invention, as is clear from the results shown in Table 1, when used as the base material of the expanded PVC cushion floor, the surface smoothness and the interlayer It is possible to obtain a sheet material having excellent peeling strength, anti-strikethrough of polyvinyl chloride sol, and excellent adhesiveness with the sol.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 D21H 13/40 27/00 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Internal reference number FI technical display location D21H 13/40 27/00

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 主としてガラス繊維およびパルプから形
成されるシートにおいて,該シートの2次加工用バイン
ダーとしてカチオン変性芳香族ポリウレタン樹脂が使用
され,前記ポリウレタン樹脂の含浸量が,シート重量に
対して5から20重量%であることを特徴とするシート
材料。
1. A sheet formed mainly of glass fibers and pulp, wherein a cation-modified aromatic polyurethane resin is used as a binder for secondary processing of the sheet, and the impregnation amount of the polyurethane resin is 5 relative to the sheet weight. To 20% by weight of the sheet material.
JP5718593A 1993-03-17 1993-03-17 Sheet material Pending JPH06272193A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5718593A JPH06272193A (en) 1993-03-17 1993-03-17 Sheet material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5718593A JPH06272193A (en) 1993-03-17 1993-03-17 Sheet material

Publications (1)

Publication Number Publication Date
JPH06272193A true JPH06272193A (en) 1994-09-27

Family

ID=13048447

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5718593A Pending JPH06272193A (en) 1993-03-17 1993-03-17 Sheet material

Country Status (1)

Country Link
JP (1) JPH06272193A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006087426A1 (en) * 2005-02-15 2006-08-24 Ahlstrom Glassfibre Oy A method of manufacturing a carrier substrate for cv flooring, a carrier substrate for cv flooring and cv flooring

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006087426A1 (en) * 2005-02-15 2006-08-24 Ahlstrom Glassfibre Oy A method of manufacturing a carrier substrate for cv flooring, a carrier substrate for cv flooring and cv flooring

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