JPH11957A - Three dimensionally molded sheet - Google Patents
Three dimensionally molded sheetInfo
- Publication number
- JPH11957A JPH11957A JP15480797A JP15480797A JPH11957A JP H11957 A JPH11957 A JP H11957A JP 15480797 A JP15480797 A JP 15480797A JP 15480797 A JP15480797 A JP 15480797A JP H11957 A JPH11957 A JP H11957A
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- pva
- sheet
- binder
- weight
- 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
Landscapes
- Laminated Bodies (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明はコルゲート体、波形
紙、ハニカム構造体等の立体成形用シートに関するもの
である。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a three-dimensionally formed sheet such as a corrugated body, corrugated paper, or a honeycomb structure.
【0002】[0002]
【従来の技術】従来段ボール等のコルゲート体、波形
紙、ハニカム構造体、その他に用いる立体成形用シート
を形成する為には、その原紙中にパルプやウール状の有
機または無機繊維を混入して成形性を付与する必要があ
った。これは、加工したい形状に変形した状態で加熱加
圧することによって、繊維の物理的な絡まりを強固なも
のとし、成形性を高める効果を狙ったものである。2. Description of the Related Art Conventionally, in order to form a corrugated body such as a corrugated cardboard, corrugated paper, a honeycomb structure, and a three-dimensional forming sheet used for other materials, pulp or wool-like organic or inorganic fibers are mixed into the base paper. It was necessary to impart moldability. This aims at strengthening the physical entanglement of the fibers by heating and pressing in a state where the fibers are deformed into a shape to be processed, and aims at an effect of enhancing the formability.
【0003】特にセルロースパルプをシートの構成成分
として含有する場合には、繊維の絡まりと水素結合で非
常に高度なセット性が得られるため、段ボールに使用さ
れる中芯等をはじめとして、これまで多くの立体成形用
シートとして使用されてきた。また有機または無機繊維
のウール状繊維の場合にも、これまで成形性があること
を利用した使用法があった。[0003] In particular, when cellulose pulp is contained as a constituent component of a sheet, very high setting properties can be obtained by entanglement of fibers and hydrogen bonding. It has been used as many three-dimensional molding sheets. Also, in the case of wool fibers of organic or inorganic fibers, there has been a method of using the fact that they have moldability.
【0004】しかしながら、例えばチョップドストラン
ドの形状をもつ繊維で全て構成される不織布等では、こ
の様な立体成形性を期待できない。不織布もその使用用
途や使用条件によっては、パルプやウール状繊維を混入
しない構成となることも考えられるので、この様な場合
には繊維の絡まりまたは水素結合による立体成形時の成
形性を付与することは困難であった。[0004] However, such a three-dimensional formability cannot be expected in a non-woven fabric or the like composed entirely of fibers having a chopped strand shape. Depending on the application and conditions of use, the non-woven fabric may have a configuration in which pulp and wool-like fibers are not mixed. In such a case, the moldability during three-dimensional molding due to fiber entanglement or hydrogen bonding is imparted. It was difficult.
【0005】或いは別の方法として、不織布を構成する
繊維の軟化点または融点以上の温度で加熱加圧し、シー
トを立体成形することもできる。この場合、パルプやウ
ール状繊維を混入しないで成形性が得られるという点で
非常に有意義であるが、無機繊維のように軟化点または
融点が非常に高温の場合は、これを熱融着して成形性を
持たせるのは実際的でない。[0005] Alternatively, as another method, the sheet can be three-dimensionally molded by heating and pressing at a temperature higher than the softening point or melting point of the fibers constituting the nonwoven fabric. In this case, it is very significant in that moldability can be obtained without mixing pulp or wool-like fiber.However, when the softening point or melting point is very high, such as inorganic fiber, heat-fusion is performed. It is not practical to provide moldability.
【0006】[0006]
【発明が解決しようとする課題】したがって、成形容易
な立体成形用シートに要求される条件として、以下の項
目が考えられる。・比較的低温で成形加工できること。
どのような形態の繊維にも適用できること。・好ましく
は成形後の加工効果が持続されること。Therefore, the following items can be considered as conditions required for a three-dimensionally molded sheet that can be easily molded.・ Mould be formed at relatively low temperature.
Applicable to any form of fiber. -Preferably, the processing effect after molding is maintained.
【0007】[0007]
【課題を解決するための手段】本発明者等は、バインダ
ーとしてポリビニルアルコール成分(以下PVA成分と
いう)を用いた立体成形用シートが、比較的低温の熱圧
着で非常に立体成形性に優れており、かつバインダーと
しての効果を併せもつため、高強度の成形体が得られる
ことを見いだして本発明に到達した。Means for Solving the Problems The present inventors have found that a three-dimensional molding sheet using a polyvinyl alcohol component (hereinafter referred to as a PVA component) as a binder has very excellent three-dimensional moldability by thermocompression bonding at a relatively low temperature. In addition, the present inventors have found that a high-strength molded article can be obtained because of having a high effect as a binder.
【0008】すなわち本発明は、有機または無機繊維か
らなる主体繊維と、バインダーであるポリビニルアルコ
ール成分とから構成される立体成形用シートに関するも
のである。また本発明は、有機または無機繊維からなる
主体繊維50〜97重量%と、ポリビニルアルコール成
分繊維3〜50重量%とから構成される立体成形用シー
トに関するものである。本明細書において、主体繊維、
PVA成分の重量%は、立体成形用シートの重量を10
0とした場合の割合である。[0008] That is, the present invention relates to a three-dimensional molding sheet comprising main fibers composed of organic or inorganic fibers and a polyvinyl alcohol component as a binder. The present invention also relates to a three-dimensional molding sheet comprising 50 to 97% by weight of main fibers made of organic or inorganic fibers and 3 to 50% by weight of polyvinyl alcohol component fibers. In the present specification, the main fiber,
The weight% of the PVA component is calculated by subtracting the weight of the three-dimensional molding sheet by 10%.
This is the ratio when 0 is set.
【0009】[0009]
【発明の実施の形態】本発明においてバインダーとして
用いられるPVA成分としては、ポリビニルアルコール
(以下PVA)繊維、PVA粉末または液状PVA等が
ある。また本発明のPVA成分にはポリ酢酸ビニルをア
ルカリ、酸、アンモニア水などで部分ケン化することに
より得られる高分子化合物であって、ポバールと呼ばれ
るものも含まれる。上記ポバールのケン化度は限定され
ないが、部分ケン化されたPVA40〜100重量%とポリ酢
酸ビニル0〜60重量%で構成されるものが好ましい。BEST MODE FOR CARRYING OUT THE INVENTION As the PVA component used as a binder in the present invention, there are polyvinyl alcohol (hereinafter referred to as PVA) fiber, PVA powder or liquid PVA. Further, the PVA component of the present invention includes a polymer compound obtained by partially saponifying polyvinyl acetate with an alkali, an acid, aqueous ammonia, or the like, and also includes a so-called poval. Although the degree of saponification of the above-mentioned poval is not limited, it is preferable that the PVA is composed of 40 to 100% by weight of partially saponified PVA and 0 to 60% by weight of polyvinyl acetate.
【0010】さらにまた、本発明のPVA成分にはPV
A誘導体も含まれる。例えばPVA繊維、PVA粉末ま
たは液状PVAを部分アセタール化することによって耐
熱性を改良したものもがビニロンの名で市販されている
が、これも良好な成形性を有し、本発明のPVA成分に
含まれる。Further, the PVA component of the present invention includes PV
A derivatives are also included. For example, those having improved heat resistance by partially acetalizing PVA fiber, PVA powder or liquid PVA are also commercially available under the name of Vinylon, which also have good moldability, and are used in the PVA component of the present invention. included.
【0011】実際には、 PVA繊維またはPVA粉末
を主体繊維と混抄する場合、或いは液状PVAを含浸ま
たは塗工する場合、シートを水分をもたせた状態でいっ
たん加熱乾燥する。こうすることで、 PVA繊維は加
熱過程でシート中の熱水にいったん溶解し、その後乾燥
することになる。 この結果、 PVA成分を主体繊維表
面のすみずみにまでいきわたらせるが、特に主体繊維の
交点に多く存在するようになるため、熱圧着による立体
成形性が高まる。また主体繊維とPVA成分を強固に結
合させることが出来るので、バインダー効果も発揮でき
る。In practice, when PVA fiber or PVA powder is mixed with the main fiber, or when liquid PVA is impregnated or coated, the sheet is heated and dried once with moisture. By doing so, the PVA fibers are once dissolved in the hot water in the sheet during the heating process and then dried. As a result, the PVA component is spread to every corner of the surface of the main fiber. However, since the PVA component is particularly present at the intersections of the main fiber, the three-dimensional formability by thermocompression bonding is enhanced. Further, since the main fiber and the PVA component can be firmly bonded, a binder effect can also be exhibited.
【0012】本発明の立体成形用シートは有機または無
機繊維からなる主体繊維50〜97重量%と、PVA成
分3〜50重量%とから構成されることが望ましい。P
VA成分が3重量%に満たないと十分な成形性が得られ
ないし、バインダーとしての効果も十分には期待できな
い。逆にPVA成分が50重量%をこえると主体繊維の
本数が少ないため、加熱加圧成形後に充分なシート強度
が得られない。The three-dimensionally formed sheet of the present invention is desirably composed of 50 to 97% by weight of main fibers made of organic or inorganic fibers and 3 to 50% by weight of a PVA component. P
If the content of the VA component is less than 3% by weight, sufficient moldability cannot be obtained and the effect as a binder cannot be expected sufficiently. Conversely, if the PVA component exceeds 50% by weight, the number of the main fibers is small, so that sufficient sheet strength cannot be obtained after hot press molding.
【0013】本発明の立体成形用シートはバインダーと
してPVA成分を用いることが肝要であり、それによっ
て本発明の目的を達成することが出来る。たとえばバイ
ンダーとしてアクリル樹脂のような硬い樹脂を用いた場
合は、主体繊維同志を結合する部分が硬すぎて柔軟性に
欠け、コルゲート時にセット性が悪い。オレフィンのよ
うな柔らかい樹脂では樹脂自体の弾性が低く、セット後
の主体繊維の反発力で結合部分が変形してしまい、コル
ゲート性が総じて高くならない。It is important that the three-dimensionally formed sheet of the present invention uses a PVA component as a binder, whereby the object of the present invention can be achieved. For example, when a hard resin such as an acrylic resin is used as a binder, a portion connecting the main fibers is too hard and lacks flexibility, and the setting property at the time of corrugation is poor. With a soft resin such as olefin, the elasticity of the resin itself is low, and the bonded portion is deformed by the repulsive force of the main fiber after setting, so that the corrugating property does not generally increase.
【0014】またフェノール樹脂のような熱硬化性樹脂
を用いた場合には、硬化度のコントロールが難しく、未
硬化のシートを用いると低温(80℃付近)での熱可塑
のため、コルゲーターロールにべたべたとくっついてし
まい、作業性が悪く、また硬化度の進んだものは、セッ
ト性が悪い。When a thermosetting resin such as a phenolic resin is used, it is difficult to control the degree of curing. If an uncured sheet is used, it is thermoplastic at a low temperature (around 80 ° C.). It sticks to stickiness and is poor in workability, and those with advanced curing degree have poor setability.
【0015】本発明における「主体繊維」は不織布構造
体の骨格をなす成分であり、主体繊維の素材は、有機、
無機を問わずあらゆる素材が該当する。ただし、主体繊
維の融点または軟化点が65〜85℃となると、PVA成分
のガラス転移温度と同一かまたはそれよりも低くなって
しまうため、主体繊維の融点または軟化点はこの温度以
上でなければならない。また、本発明で使用する主体繊
維の形状は、チョップドストランド、パルプ、ウール
状、ウィスカー等様々なものが該当し、特に限定するも
のではない。The "main fiber" in the present invention is a component constituting the skeleton of the nonwoven fabric structure.
All materials are applicable regardless of inorganic. However, if the melting point or softening point of the main fiber is 65 to 85 ° C., it becomes equal to or lower than the glass transition temperature of the PVA component. Therefore, the melting point or softening point of the main fiber must be equal to or higher than this temperature. No. Further, the shape of the main fiber used in the present invention corresponds to various types such as chopped strand, pulp, wool, whisker, and is not particularly limited.
【0016】本発明の立体成形用シートは例えばコルゲ
ーター等で熱圧着されることによって立体成形品とな
る。本発明において熱圧着の温度は特に限定しないが、
PVA成分のガラス転移温度が約65℃〜85℃であること
から、この温度よりも高温で熱圧着すれば、シートに対
して立体成形性を発現する。しかし実際に十分な立体成
形性を発現するためには、この温度よりも高温の約100
℃以上で熱圧着を行う必要がある。一方あまり高温にす
ると200℃以上でPVA成分の収縮がはじまり220〜230
℃で軟化点に至るため、この温度域以上になると軟化収
縮しながら徐々に燃焼を開始する。したがって、熱圧着
の温度は高温になり過ぎない方が好ましい。The three-dimensional molded sheet of the present invention is formed into a three-dimensional molded product by thermocompression bonding using, for example, a corrugator. In the present invention, the temperature of thermocompression bonding is not particularly limited,
Since the glass transition temperature of the PVA component is about 65 ° C. to 85 ° C., if the thermocompression bonding is performed at a temperature higher than this temperature, three-dimensional moldability is exhibited for the sheet. However, in order to actually exhibit sufficient three-dimensional moldability, a temperature higher than this temperature of about 100
It is necessary to perform thermocompression bonding at a temperature of ℃ or more. On the other hand, if the temperature is too high, the shrinkage of the PVA component starts at 200 ° C.
Since the temperature reaches the softening point at ° C, when the temperature exceeds this temperature range, the combustion gradually starts while softening and shrinking. Therefore, the temperature of thermocompression bonding is preferably not too high.
【0017】[0017]
【実施例】次に、本発明を以下の実施例にしたがって具
体的に説明する。Next, the present invention will be described specifically with reference to the following examples.
【0018】実施例1 Eガラス製ガラス繊維チョップドストランド(ユニチカ
株式会社製、繊維径φ6μm、繊維長6 mm )80重量%を
主体繊維とし、バインダーとしてPVA繊維20重量%を
混合したスラリーを有効固形分濃度0.1wt%で準備し、こ
れを湿式法で混抄して湿式不織布を得た。得られた湿式
不織布を145℃で乾燥し、PVA繊維の溶解により繊維
同士を結合固着してシート化した。このシートを本発明
の立体成形用シートとした。その特性値を表1に示す。Example 1 E-glass glass fiber chopped strand (produced by Unitika Ltd., fiber diameter φ6 μm, fiber length 6 mm) was used as a main fiber, and a slurry obtained by mixing 20% by weight of PVA fiber as a binder was used as an effective solid. It was prepared at a partial concentration of 0.1 wt%, and mixed with a wet method to obtain a wet nonwoven fabric. The obtained wet nonwoven fabric was dried at 145 ° C., and the fibers were bonded and fixed by dissolution of PVA fibers to form a sheet. This sheet was used as the three-dimensionally formed sheet of the present invention. Table 1 shows the characteristic values.
【0019】次にこの立体成形用シートを段ボール加工
機により180℃でコルゲート加工し、加工後のコルゲー
ト戻り率を計算した。 コルゲート戻り率 (%) =[(コルゲート後の実測長−コ
ルゲート後の理論長)/ (コルゲート前の実測長−コル
ゲート後の理論長)]×100Next, the three-dimensionally formed sheet was corrugated at 180 ° C. by a corrugated cardboard processing machine, and the corrugated return rate after the processing was calculated. Corrugated return rate (%) = [(measured length after corrugate-theoretical length after corrugate) / (actual length before corrugate-theoretical length after corrugate)] x 100
【0020】また、この立体成形用シートを段ロールの
表面温度を変えてコルゲート加工し、その時のコルゲー
ト戻り率を測定して図1にまとめた(コルゲーターのピ
ッチ=8.56mm)。Further, the three-dimensionally formed sheet was corrugated by changing the surface temperature of the step roll, and the corrugated return rate at that time was measured and summarized in FIG. 1 (corrugator pitch = 8.56 mm).
【0021】実施例2 Eガラス製ガラス繊維チョップドストランド(ユニチカ
株式会社製、繊維径φ6μm、繊維長6 mm )65重量%
と、セラミック繊維(繊維径2〜3μm)25重量%からな
る主体繊維を混合し、バインダーとしてPVA繊維10重
量%を混合したスラリーを有効固形分濃度0.1wt%で準備
し、これを湿式法で混抄して湿式不織布を得た。得られ
た湿式不織布を145℃で乾燥し、PVA繊維の溶解によ
り繊維同士を結合固着してシート化した。このシートを
本発明の立体成形用シートとした。さらにこのシートを
用いて実施例1と同様にしてコルゲート加工し、コルゲ
ート戻り率を測定した。立体成形用シートの特性値およ
びコルゲート加工後のコルゲート戻り率を表1に示す。Example 2 E-glass glass fiber chopped strand (produced by Unitika Ltd., fiber diameter φ6 μm, fiber length 6 mm) 65% by weight
And a main fiber composed of 25% by weight of ceramic fiber (fiber diameter 2-3 μm), and a slurry containing 10% by weight of PVA fiber as a binder is prepared at an effective solid content of 0.1% by weight. The mixture was mixed to obtain a wet nonwoven fabric. The obtained wet nonwoven fabric was dried at 145 ° C., and the fibers were bonded and fixed by dissolution of PVA fibers to form a sheet. This sheet was used as the three-dimensionally formed sheet of the present invention. Further, using this sheet, corrugating was performed in the same manner as in Example 1, and the corrugated return rate was measured. Table 1 shows the characteristic values of the three-dimensionally formed sheet and the corrugated return rate after corrugating.
【0022】比較例1 Eガラス製円形断面ガラス繊維チョップドストランド
(日本電気ガラス株式会社製、繊維径φ9μm、繊維長13
mm)98重量%を主体繊維とし、バインダーとしてPVA
繊維2重量%を混合したスラリーを有効固形分濃度0.1wt
%で準備した。その後は実施例1と全く同じ条件で立体
成形用シートを作成し、さらにコルゲート加工をおこな
った。また同じ項目について測定した。立体成形用シー
トの特性値およびコルゲート加工後のコルゲート戻り率
を表1に示す。Comparative Example 1 E glass circular cross section glass fiber chopped strand (manufactured by NEC Corporation, fiber diameter φ9 μm, fiber length 13)
mm) 98% by weight as main fiber and PVA as binder
A slurry containing 2% by weight of fibers is mixed with an effective solid content of 0.1 wt.
% Prepared. Thereafter, a three-dimensionally formed sheet was prepared under exactly the same conditions as in Example 1, and further corrugated. The same items were measured. Table 1 shows the characteristic values of the three-dimensionally formed sheet and the corrugated return rate after corrugating.
【0023】比較例2 Eガラス製円形断面ガラス繊維チョップドストランド
(日本電気ガラス株式会社製、繊維径φ9μm、繊維長13
mm)90重量%を主体繊維とし、バインダーとして熱融着
性芯鞘オレフィンバインダー繊維10重量%(大和紡績株
式会社製、繊維径φ0.9 de、繊維長5 mm)を混合したス
ラリーを有効固形分濃度0.1wt%で準備した。その後は実
施例1と全く同じ条件で立体成形用シートを作成し、さ
らにコルゲート加工をおこなった。また同じ項目につい
て測定した。立体成形用シートの特性値およびコルゲー
ト加工後のコルゲート戻り率を表1に示す。Comparative Example 2 E glass circular cross section glass fiber chopped strand (manufactured by NEC Corporation, fiber diameter φ9 μm, fiber length 13)
mm) 90% by weight as the main fiber and a slurry obtained by mixing 10% by weight of heat-fusible core-sheath olefin binder fiber (Daiwa Spinning Co., Ltd., fiber diameter φ0.9 de, fiber length 5 mm) as a binder It was prepared with a concentration of 0.1 wt%. Thereafter, a three-dimensionally formed sheet was prepared under exactly the same conditions as in Example 1, and further corrugated. The same items were measured. Table 1 shows the characteristic values of the three-dimensionally formed sheet and the corrugated return rate after corrugating.
【0024】比較例3 Eガラス製円形断面ガラス繊維チョップドストランド
(日本電気ガラス株式会社製、繊維径φ9μm、繊維長13
mm)90重量%を主体繊維とし、そのスラリーを有効固形
分濃度0.1wt%で湿式法で抄紙して湿式不織布を得た。こ
の湿式不織布の湿紙の状態でバインダーとしてアクリル
樹脂のエマルジョン10重量%をスプレーした。その後は
実施例1と全く同じ条件で立体成形用シートを作成し、
さらにコルゲート加工をおこなった。また同じ項目につ
いて測定した。立体成形用シートの特性値およびコルゲ
ート加工後のコルゲート戻り率を表1に示す。Comparative Example 3 E glass circular cross section glass fiber chopped strand (manufactured by NEC Corporation, fiber diameter φ9 μm, fiber length 13)
mm) 90% by weight as a main fiber, and the slurry was wet-processed at an effective solid content of 0.1% by weight to obtain a wet nonwoven fabric. 10% by weight of an emulsion of an acrylic resin was sprayed as a binder in the state of this wet nonwoven wet paper. After that, a sheet for three-dimensional molding was created under exactly the same conditions as in Example 1,
Furthermore, corrugated processing was performed. The same items were measured. Table 1 shows the characteristic values of the three-dimensionally formed sheet and the corrugated return rate after corrugating.
【0025】比較例4 Eガラス製円形断面ガラス繊維チョップドストランド
(日本電気ガラス株式会社製、繊維径φ9μm、繊維長13
mm)90重量%を主体繊維とし、バインダーとしてフェノ
ール樹脂粉末10重量%を混合したスラリーを有効固形分
濃度0.1wt%で準備した。その後は実施例1と全く同じ条
件で立体成形用シートを作成し、さらにコルゲート加工
をおこなった。また同じ項目について測定した。立体成
形用シートの特性値およびコルゲート加工後のコルゲー
ト戻り率を表1に示す。Comparative Example 4 E glass circular cross section glass fiber chopped strand (manufactured by NEC Corporation, fiber diameter φ9 μm, fiber length 13)
mm) A slurry containing 90% by weight of a main fiber and 10% by weight of a phenol resin powder as a binder was prepared at an effective solid content of 0.1% by weight. Thereafter, a three-dimensionally formed sheet was prepared under exactly the same conditions as in Example 1, and further corrugated. The same items were measured. Table 1 shows the characteristic values of the three-dimensionally formed sheet and the corrugated return rate after corrugating.
【0026】比較例5 Eガラス製円形断面ガラス繊維チョップドストランド
(日本電気ガラス株式会社製、繊維径φ9μm、繊維長13
mm)90重量%と、NBKPパルプ(Crestbrook Forest Indu
stry社製、フリーネス250ml)10重量%からなる主体繊
維を混合したスラリーを有効固形分濃度0.1wt%で準備し
た。(バインダーは入れなかった)その後は実施例1と
全く同じ条件で立体成形用シートを作成し、さらにコル
ゲート加工をおこなった。また同じ項目について測定し
た。立体成形用シートの特性値およびコルゲート加工後
のコルゲート戻り率を表1に示す。Comparative Example 5 E glass circular cross section glass fiber chopped strand (manufactured by NEC Corporation, fiber diameter φ9 μm, fiber length 13)
mm) 90% by weight and NBKP pulp (Crestbrook Forest Indu
A slurry containing 10% by weight of a main fiber composed of 10% by weight (freeness 250 ml, manufactured by stry) was prepared at an effective solid content of 0.1% by weight. Thereafter, a sheet for three-dimensional molding was prepared under exactly the same conditions as in Example 1 and further corrugated. The same items were measured. Table 1 shows the characteristic values of the three-dimensionally formed sheet and the corrugated return rate after corrugating.
【0027】[0027]
【表1】 [Table 1]
【0028】[0028]
【発明の効果】本発明の立体成形用シートは、PVAバ
インダーとしての効果でシート強度自体の向上が図られ
る。強度向上は、主体繊維の交点にPVA成分が存在す
ることによって、1交点について2本以上の主体繊維を
つなぎ止めることによるものである。強度向上は3次元
的に硬化を発揮するが、主体繊維自体の強度が低い場合
には最大強度はこれに依存することになる。According to the three-dimensionally formed sheet of the present invention, the sheet strength itself can be improved by the effect as a PVA binder. The improvement in strength is due to the presence of the PVA component at the intersections of the main fibers, thereby securing two or more main fibers at one intersection. The strength is enhanced three-dimensionally, but when the strength of the main fiber itself is low, the maximum strength depends on this.
【0029】本発明によれば、比較的低温の熱圧着で非
常に高度な成形性を示す立体成形用シートを得ることが
できる。According to the present invention, it is possible to obtain a three-dimensionally formed sheet having extremely high formability by thermocompression bonding at a relatively low temperature.
【図1】は実施例1の段ロールの表面温度とコルゲート
戻り率の関係を表す図である。FIG. 1 is a diagram showing the relationship between the surface temperature of a step roll and a corrugated return rate in Example 1.
Claims (2)
バインダーであるポリビニルアルコール成分とから構成
される立体成形用シート。1. A main fiber comprising an organic or inorganic fiber,
A three-dimensional molding sheet comprising a binder and a polyvinyl alcohol component.
〜97重量%と、ポリビニルアルコール成分繊維3〜5
0重量%とから構成される請求項1の立体成形用シー
ト。2. A main fiber 50 comprising an organic or inorganic fiber.
To 97% by weight, and polyvinyl alcohol component fibers 3 to 5
The three-dimensionally formed sheet according to claim 1, comprising 0% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15480797A JP3356003B2 (en) | 1997-06-12 | 1997-06-12 | 3D molding sheet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15480797A JP3356003B2 (en) | 1997-06-12 | 1997-06-12 | 3D molding sheet |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH11957A true JPH11957A (en) | 1999-01-06 |
JP3356003B2 JP3356003B2 (en) | 2002-12-09 |
Family
ID=15592322
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP15480797A Expired - Lifetime JP3356003B2 (en) | 1997-06-12 | 1997-06-12 | 3D molding sheet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3356003B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4654384A (en) * | 1983-01-14 | 1987-03-31 | Ciba-Geigy Corporation | Basic water-soluble bis-(β-azo-α-naphtholamino)-triazine compounds |
-
1997
- 1997-06-12 JP JP15480797A patent/JP3356003B2/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4654384A (en) * | 1983-01-14 | 1987-03-31 | Ciba-Geigy Corporation | Basic water-soluble bis-(β-azo-α-naphtholamino)-triazine compounds |
Also Published As
Publication number | Publication date |
---|---|
JP3356003B2 (en) | 2002-12-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5772846A (en) | Nonwoven glass fiber mat for facing gypsum board and method of making | |
US6165921A (en) | Fibrous acoustical material for reducing noise transmission and method for producing the same | |
US5516580A (en) | Cellulosic fiber insulation material | |
EP1678385B1 (en) | A cellulose fibre based insulation material | |
NL8220157A (en) | FIBER MAT, METHOD FOR MANUFACTURING THE SAME AND AN OBJECT MADE THEREOF | |
JP2020037710A (en) | Sheet for fiber-reinforced plastic molded body and method of molding thereof | |
JP3356003B2 (en) | 3D molding sheet | |
JP2010284986A (en) | Sound absorbing laminated material and sound absorbing laminated material mold | |
JP3186498B2 (en) | Bundled fiber for cement reinforcement | |
JP2007204896A (en) | Fiber sheet and method for producing the same | |
JP2005526188A (en) | Natural and fiberglass mat | |
JP2011116086A (en) | Reinforcing sheet and sheet-like structural material using the same | |
JP2006273962A (en) | Acrylic resin composition, sheet forming material containing basalt fiber, board material and interior material for automobile | |
JPS6333991Y2 (en) | ||
JP5185058B2 (en) | Dry nonwoven fabric | |
JP3743470B2 (en) | Fiber sheet and fiber sheet molding | |
JPH058125Y2 (en) | ||
JP3274869B2 (en) | Feather sheet and method of using the same | |
JP2955872B2 (en) | Water-disintegratable nonwoven fabric and method for producing the same | |
JPH0931815A (en) | Fiber aggregate and its production | |
JP6675650B2 (en) | Fiber sheet for intermediate reinforcing material of vinyl chloride resin building material and method for producing the same | |
JP3174825B2 (en) | Silk fiber paper, method for producing the same, and molded product using silk fiber paper | |
JP4301845B2 (en) | Hemp blended sheet | |
JP2542166B2 (en) | Decorative synthetic resin plate with excellent moldability | |
JP2006200044A (en) | Vulcanized fiber having low density and excellent dimensional stability and method for producing the same |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20081004 Year of fee payment: 6 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20091004 Year of fee payment: 7 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20091004 Year of fee payment: 7 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20101004 Year of fee payment: 8 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20101004 Year of fee payment: 8 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20111004 Year of fee payment: 9 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20121004 Year of fee payment: 10 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20131004 Year of fee payment: 11 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20131004 Year of fee payment: 11 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20141004 Year of fee payment: 12 |
|
EXPY | Cancellation because of completion of term |