JPH01501859A - Low density mineral wool panel and its manufacturing method - Google Patents

Low density mineral wool panel and its manufacturing method

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Publication number
JPH01501859A
JPH01501859A JP63501569A JP50156988A JPH01501859A JP H01501859 A JPH01501859 A JP H01501859A JP 63501569 A JP63501569 A JP 63501569A JP 50156988 A JP50156988 A JP 50156988A JP H01501859 A JPH01501859 A JP H01501859A
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Prior art keywords
mineral wool
panel
starch
aggregates
approximately
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JP63501569A
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Japanese (ja)
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アイザード,テビツド グラハム
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ユーエスジー インテリアーズ,インコーポレーテツド
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    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/21Macromolecular organic compounds of natural origin; Derivatives thereof
    • D21H17/22Proteins
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21FPAPER-MAKING MACHINES; METHODS OF PRODUCING PAPER THEREON
    • D21F11/00Processes for making continuous lengths of paper, or of cardboard, or of wet web for fibre board production, on paper-making machines
    • D21F11/002Processes for making continuous lengths of paper, or of cardboard, or of wet web for fibre board production, on paper-making machines by using a foamed suspension
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21FPAPER-MAKING MACHINES; METHODS OF PRODUCING PAPER THEREON
    • D21F11/00Processes for making continuous lengths of paper, or of cardboard, or of wet web for fibre board production, on paper-making machines
    • D21F11/02Processes for making continuous lengths of paper, or of cardboard, or of wet web for fibre board production, on paper-making machines of the Fourdrinier type
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H13/00Pulp or paper, comprising synthetic cellulose or non-cellulose fibres or web-forming material
    • D21H13/36Inorganic fibres or flakes
    • D21H13/38Inorganic fibres or flakes siliceous
    • D21H13/40Inorganic fibres or flakes siliceous vitreous, e.g. mineral wool, glass fibres
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/21Macromolecular organic compounds of natural origin; Derivatives thereof
    • D21H17/24Polysaccharides
    • D21H17/28Starch
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/21Macromolecular organic compounds of natural origin; Derivatives thereof
    • D21H17/24Polysaccharides
    • D21H17/31Gums
    • D21H17/32Guar or other polygalactomannan gum
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21JFIBREBOARD; MANUFACTURE OF ARTICLES FROM CELLULOSIC FIBROUS SUSPENSIONS OR FROM PAPIER-MACHE
    • D21J1/00Fibreboard
    • D21J1/16Special fibreboard
    • D21J1/20Insulating board

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  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Paper (AREA)
  • Laminated Bodies (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるため要約のデータは記録されません。 (57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 低密度ミネラルウールパネル及びその製造法技術分野 本発明はミネラルウール繊維製品の製造法、特に密度が立方フィート当たり約3 〜10ボンド(50〜160kg/m”)程度の極めて軽量なミネラルウール繊 維で作られ、吸音天井タイル、断熱パネル、吸音パネル、ビーム音等の防音・耐 熱製品として使用される建造物等の構造材用の強固なパネルの製造法に関する。[Detailed description of the invention] Low-density mineral wool panel and its manufacturing method Technical field The present invention relates to a method for producing mineral wool fiber products, particularly those having a density of about 3 per cubic foot. Extremely lightweight mineral wool fiber of ~10 bond (50-160 kg/m”) Soundproofing and resistance to sound absorption ceiling tiles, insulation panels, sound absorption panels, beam sound, etc. This paper relates to a method for manufacturing strong panels for structural materials such as buildings used as thermal products.

背景技術 ミネラルウール及び軽1凝結体からなる希釈水性分散液の水フェルトを用いる構 成は周知である。当該分散液を多孔構造の移動支承ワイヤベルトに流し重力を利 用し、次いで減圧吸収装置により脱水し、これにより得られた湿潤マットはまだ 60〜80%の水分を含んでいるから、熱対流炉内で長時間乾燥し、且つこれに よって作成されたマットを切断し、必要に応じ塗料等で表面処理を施し、吸音天 井製品等の軽量な構造材用のパネルを作成する。Background technology Construction using water felt of a dilute aqueous dispersion of mineral wool and light aggregates The formation is well known. The dispersion liquid is poured into a moving support wire belt with a porous structure and gravity is used to The resulting wet mat is still Since it contains 60 to 80% moisture, it is dried in a convection oven for a long time, and The mats thus created are cut, surface treated with paint, etc. as necessary, and sound-absorbing ceilings are installed. Create panels for lightweight structural materials such as well products.

一部ミネラルウールにより安定させたフオーム材を作ることも知られている。例 えば米国特許第4.447.560号には、合成ゴムラフテックス固形体を含む 第1の繊維スラリを作成し、低密度の絶縁シートを作成する方法が提案されてい る。この場合更に洗浄剤スラリを作り、これらのスラリを15%固形分の粗度に なるよう混合し、撹拌して安定したフオーム材を作り、次いで炉において乾燥す る。しかしながら、この方法では製品の作成に極めて多くの時間を要し、15% 固形分から安定したフオーム材を乾燥形成するには多大のエネルギを必要として 、経済上の見地から好ましくない。It is also known to make foams stabilized in part by mineral wool. example For example, U.S. Pat. No. 4,447,560 includes synthetic rubber roughtex solids. A method is proposed to create a first fiber slurry and create a low density insulation sheet. Ru. In this case, further detergent slurries are made and these slurries are reduced to a coarseness of 15% solids. Mix and stir to form a stable foam, then dry in an oven. Ru. However, this method requires significantly more time to create the product, with 15% It takes a lot of energy to dry and form a stable foam from solids. , which is unfavorable from an economic point of view.

また米国特許第3.228.825号には、繊細化されたガラス繊維で作られる 軽量フオーム材を用いて立方フィート当たり約1〜3ボンド(16〜50 kg /m3)の密度を有する極めて軽量なバイブラップ(pipe wrap)を製 造する方法が提案されている。この発泡体は例えば吊下用の天井格子にパネルの 縁部でのみ支承されても自重で視認可能な程度の垂下、弯曲あるいは破損を来た さないことが要求される“構造材用”としては不向きである。当該米国特許にお いては、微細な泡を作り、高純度に精製したセルロース系フイブリドの“結合繊 維”接着剤により軽量凝結体と繊細化されたガラス繊維とを均等に混合して泡を 内包する混合物を得る。U.S. Pat. No. 3,228,825 also states that Approximately 1 to 3 bonds per cubic foot (16 to 50 kg) using lightweight foam materials We manufacture extremely lightweight pipe wrap with a density of /m3). A method has been proposed to create This foam can be used, for example, in panels for hanging ceiling grids. Even if it is supported only at the edges, it has sagged, bent, or broken to a visible degree due to its own weight. It is unsuitable for "structural materials" that require no damage. The U.S. patent The fibers are made of highly purified cellulose fibrids that create fine bubbles. Foam is created by evenly mixing lightweight aggregates and attenuated glass fibers using fiber adhesive. Obtain the encapsulating mixture.

更に、ポリアクリルアミドのような極めて少量の凝集体を加えてミネラル繊維の 希釈分散液に無機クレイを凝集することは知られている。米国特許第3.510 .394号に開示されるように、この凝集体は、繊維間で団塊となりマットの重 力による脱水の際放出される脱水液内に含まれ、スターチ及びクレイが大幅に失 われることを防止すべく、スラリの脱水の直前に加える必要がある。Additionally, very small amounts of aggregates such as polyacrylamide can be added to form mineral fibers. It is known to aggregate inorganic clays in dilute dispersions. U.S. Patent No. 3.510 .. As disclosed in No. 394, this aggregate forms clumps between the fibers and increases the weight of the mat. Contained in the dehydrated liquid released during dehydration by force, starch and clay are significantly lost. It must be added just before the slurry is dehydrated to prevent it from being washed away.

更に米国特許第4.062.721号には、マットをワイヤベルトに載置し、最 初に重力により脱水する際の発泡を極力最小限に押さえ、以下の工程において発 泡可能にし、形成ボックス内での発泡を避ける構成が開示されている。Further, U.S. Pat. No. 4,062,721 discloses that the mat is placed on a wire belt and We minimize foaming during the initial gravity dehydration process, and then we try to minimize foaming in the following steps. A configuration is disclosed that allows foaming and avoids foaming within the forming box.

本発明の−の目的は密度が立方フィート当たり約3〜10ボンド(50〜160 kg/+a”)で破壊係数が平方インチ当たり約60ボンドの低密度且つ堅牢な ミネラルパネルを提供することにある。The object of the present invention is to have a density of about 3 to 10 bonds per cubic foot (50 to 160 kg/+a”) with a modulus of rupture of approximately 60 bonds per square inch. Our goal is to provide mineral panels.

本発明によれば、繊細に発砲する結合剤及び僅かにイオン結合されたカチオン・ グア(guar)ガムを実質的に非発砲の非イオン界面活性分散剤と共に混合器 に入れ、その後、ワイヤベルト部上に沈積させて繊維と絡み合わせ、多孔構造で 通し空気を通過させ得る構造体を得、更に脱水し乾燥して、極めて強固で低密度 のミネラルウールパネルを得る。本製造法によれば、脱水時間を従来の方法によ るものより低減させ、例えば吊下天井格子にパネルの縁部のみで支承されても自 重で視認可能な程度の垂下、弯曲あるいは破壊することなく支承可能な極めて密 度の低いパネルを製造し得る。According to the invention, a delicately effervescent binder and a slightly ionically bonded cationic Mixer of guar gum with a substantially non-foaming non-ionic surfactant dispersant After that, it is deposited on the wire belt section and intertwined with the fibers, creating a porous structure. Obtain a structure that allows air to pass through, and then dehydrate and dry it to create an extremely strong and low density structure. Obtain mineral wool panels. According to this production method, the dehydration time is longer than that of the conventional method. For example, even if the panels are supported only at the edge of a suspended ceiling grid, Extremely dense structures that can be supported without heavy, visible sagging, curvature, or failure. It is possible to produce panels with low degrees of strength.

エチル拳アルコール イオン・ポリエタノキシ界面活性剤を約6%プロティン残留酸分のような一部残 留プロチインを有するホイート・スターチ結合剤とトリメチルアンモニオプロピ ル・グア・クロリド・ポリマのような少量のカチオン・グア・ガム又はグア・ビ ーン・ミール誘導体とを含む組成物に加えれると、組成物を最初僅かに発砲させ ると同時に成分を互いに有効にイオン結合せしめてミネラルウールを分散させ、 ミネラルウールを絡み合わせて気孔を有する湿潤マットを得、湿潤マットから迅 速に脱水出来、且つマットに加熱された乾燥空気を早い速度で大量に通過させて 脱水を遂行し得る。ethyl fist alcohol The ionic polyethanoxy surfactant contains approximately 6% protein with some residual acid content. Wheat starch binder with distillate protiin and trimethylammoniopropylene Small amounts of cationic guar gum or guar bis, such as Le Gua Chloride Polymer When added to a composition containing a corn meal derivative, the composition initially erupts slightly. At the same time, the ingredients are effectively ionically bonded to each other and the mineral wool is dispersed. Mineral wool is intertwined to obtain a wet mat with pores, and then quickly removed from the wet mat. It can be dehydrated quickly and allows a large amount of heated dry air to pass through at a fast speed. Can perform dehydration.

図面の簡単な説明 図面は本発明によるミネラルボード製造法の簡略説明図である。Brief description of the drawing The drawing is a simplified illustration of the mineral board manufacturing method according to the present invention.

発明を実施するための最良の形態 図面に示す混合タンク10に内蔵したモータ駆動の羽根車12により、約3%〜 約6%の固形分を含む水性スラリ14を混合する。この水性スラリ14の固形分 は以下の範囲の成分からなる。BEST MODE FOR CARRYING OUT THE INVENTION Approximately 3% to An aqueous slurry 14 containing about 6% solids is mixed. Solid content of this aqueous slurry 14 consists of the following components:

成分 量 ミネラルウール 約25ル95 ホイート・スターチ 約10〜30% カチオン・グア誘導体 約0.03〜1%非イオン界面活性剤 約0.5〜3% クレイ 最大約5% 約6%プロティン分を含む市販のホイート・スターチ(例えばオギリビ・ミルズ ・インコーボレション(Ogjlyie 旧IIs, Inc.)により販売の もの)は高シェア・サイクロン混合器】8と共に混合タンク16内の一部の処理 水に分散し、約1350F〜190°F(57°C〜88°C)の温度で加熱し てスターチを煮沸する。この煮沸中スターチの粘性はそれほど大きく上昇せず、 煮沸後スターチ結合剤を混合タンク〕0へ供給する。このとき重要な点は、湿潤 マットの脱水速度及び乾燥速度を高く維持するには有害な結合剤を用いることに より、スラリの粘性がそれほど大きく上昇しないことにある。Ingredient amount Mineral wool approximately 25 ru 95 Wheat starch approximately 10-30% Cationic guar derivative: approx. 0.03~1% Nonionic surfactant: approx. 0.5~3% Clay maximum about 5% Commercially available wheat starch containing approximately 6% protein (e.g. Ogilibi Mills) ・Sold by Inc. (Ogjlyie former IIs, Inc.) ) is a high shear cyclone mixer] 8 as well as a part of the processing inside the mixing tank 16. Dispersed in water and heated to a temperature of approximately 1350F to 190F (57C to 88C). Boil the starch. The viscosity of the starch does not increase significantly during this boiling, After boiling, feed the starch binder to mixing tank〕0. At this time, the important point is To maintain high dewatering and drying rates of the mat, harmful binders may be used. This means that the viscosity of the slurry does not increase significantly.

希釈スラリ内にミネラルウール及び凝結体を良好に分散させ、多孔マットを形成 するため非イオン・ポリエタノキシ界面活性剤を混合タンク】0のスラリに加え る。この非イオン・ポリエタノキシ界面活性剤にはジ−エイ−エフ・ケミカルズ ・コーポレーション(GAF Chemicals Corporation) がら販売されている約2%溶液を使用することが好ましい。ミネラルウール及び 軽量凝結体をカチオン・グアを介しホイート・スターチ結合剤プロティンとミネ ラル面で完全に分散すべく、まスカチオン・グア・ガム誘導体凝集体を加え、ホ イート・スターチ結合剤プロティンがカチオン・グアを介してミネラル面にイオ ン結合し更にスラリをヘッドボックス3oに通過させ、ワイヤベルト部40に沈 積する前に低発泡させる。Good dispersion of mineral wool and aggregates in diluted slurry to form a porous mat Add a non-ionic polyethane surfactant to the slurry in the mixing tank Ru. This non-ionic polyethanoxy surfactant is manufactured by G.A.F. Chemicals. ・GAF Chemicals Corporation It is preferred to use an approximately 2% solution, which is sold separately. mineral wool and Light aggregates are combined with wheat starch binder protein and minerals via cationic guar. To ensure complete dispersion on the surface, add cationic guar gum derivative aggregates and Eat starch binder protein binds ions to mineral surfaces via cationic guar. Further, the slurry is passed through the head box 3o and settled on the wire belt section 40. Let it foam to a low level before laminating.

本発明に使用するミネラル繊維としては、溶融したバサルト、スラグ、花崗岩等 ガラス質ミネラル成分をオリフィスから線状に引き出して繊細化して得られるい わゆる紡織繊維、または上記の溶融したミネラル成分を紡糸ロータの面がら接線 方向に引き出して得られるいわゆるウール繊維、あるいはセラミック繊維若しく は芳香族ポリアミド繊維等を使用可能である。また本発明によりパネルを作成す る際多孔結合マット繊維を個々の繊維として使用し得る。Mineral fibers used in the present invention include molten basalt, slag, granite, etc. It is obtained by drawing out the glassy mineral component in a line from the orifice and making it delicate. The so-called textile fibers, or the above-mentioned molten mineral components, are tangential to the surface of the spinning rotor. So-called wool fibers obtained by drawing in the direction of For example, aromatic polyamide fibers can be used. Also, panels can be created according to the present invention. The porous bonded mat fibers can be used as individual fibers in the process.

軽量凝集体としては剥脱または発泡させたガラス質火山岩を用いることが好まし い。この凝集体としては、周知の如く各種のメツシュサイズのものを得れる発泡 パーライト、剥脱ひる石、剥脱クレイ等が挙げられる。一般に入手性及び経済性 の点から発泡パーライトを用いることが好ましい。It is preferable to use exfoliated or foamed glassy volcanic rock as the lightweight aggregate. stomach. As for this aggregate, as is well known, foamed material that can be obtained in various mesh sizes is used. Examples include pearlite, exfoliated vermiculite, exfoliated clay, and the like. Generally available and economical From this point of view, it is preferable to use expanded pearlite.

均質に混合されイオン結合され、僅かに発泡されたスラリをワイヤベルト部40 に沈積させて、ミネラルウール及び軽量凝結体を絡み合わせ、一定で小さな一時 的な気孔を少量存在させた多孔構造の組成物を得ることができる。この時点では 組成物内の気孔の占める割合は組成物の約10〜30容1%であり、残りの軽量 凝結体と好ましい非イオン・ポリエタノキシ界面活性剤との間の空隙は分子量が 約995のジノニルフェノ剤をなしている。同様の性質を持つ市販のエチル・ア ルコールのポリエタノキ・エーテルも使用可能である。The homogeneously mixed, ionically bonded and slightly foamed slurry is transferred to the wire belt section 40. The mineral wool and lightweight aggregates are intertwined and formed into a constant small temporary It is possible to obtain a composition having a porous structure in which a small amount of pores are present. At this point The proportion of pores in the composition is approximately 10-30% by volume, with the remaining light weight The void between the aggregates and the preferred nonionic polyethanoxy surfactant has a molecular weight of There are approximately 995 dinonylphenolic agents. Commercially available ethyl acetate with similar properties Alcohol polyester ether can also be used.

グア・2−ヒドロキー3(トリメチル−アミノ)−プロピル・エーテル・クロリ ドのようなトリメチルアンモニオプロピル・グア(ヘンケル・コーポレーション (Henkel Corporation)から販売される商標名GEND[) のポリマ粉末のカチオン・ビーン・ミール誘導体を混合タンク10に加えて水に 分散させ、また混合タンク10に直接加えたミネラルウール及び発泡パーライト のような軽量凝結体と共に凝集性あるいは固形分保持性を示す好適な濃度を有し た溶液が得られる。グア誘導体はミネラルウールを凝集する傾向を持たせる。こ の凝集効果は少量のクレイの添加により高められる。Guar 2-hydroxy 3(trimethyl-amino)-propyl ether chloride trimethylammoniopropyl gua (Henkel Corporation) Trade name GEND[) sold by (Henkel Corporation) Add the cationic bean meal derivative of polymer powder to the mixing tank 10 and add it to the water. Mineral wool and expanded perlite dispersed and added directly to the mixing tank 10 It has a suitable concentration that exhibits cohesive or solids retention properties with lightweight aggregates such as A solution is obtained. Guar derivatives give mineral wool a tendency to agglomerate. child The flocculating effect of is enhanced by the addition of small amounts of clay.

他の総ての成分を完全且つ均質に混合した後、最終的にカチオン・グア誘導体を 混合タンク10に加え数秒間混合して次にポンプ20を介し混合タンク】0から ヘッドボックス30へ送る。After thoroughly and homogeneously mixing all other ingredients, the cationic guar derivative is finally added. Add to the mixing tank 10, mix for a few seconds, then pump 20 to the mixing tank】0 to Send to head box 30.

ヘッドボックス300機能はワイヤベルト部40の幅方向に亙って均質なスラリ 層32となるよう拡布し多孔構造の湿潤マツトロ2を形成することにある。湿潤 マツトロ2の厚さは厚さ約174〜2インチの最終製品を得るのに好ましい厚さ にされる。The head box 300 function is to create a homogeneous slurry across the width of the wire belt section 40. The purpose is to spread it so as to form a layer 32 to form a wet maturo 2 having a porous structure. wet The thickness of Matsutoro 2 is the preferred thickness to obtain a final product with a thickness of approximately 174 to 2 inches. be made into

本発明の製造法において重要なことは、非イオン・ポリエタノキシ界面活性剤は その発泡性が低(、最初の混合作業において例えば混合タンク10にカチオン・ グア・ガム誘導体凝集体と共に加えて、ミネラルウール及び軽量凝結体をミネラ ル面上でカチオン・グアを介しホイート・スターチ結合剤プロティンのイオン結 合剤と完全に分散し、ヘッドボックス3゜にスラリを通す前にワイヤベルト部4 0上に低発泡性を持たせて拡布することにある。What is important in the production method of the present invention is that the nonionic polyethanoxy surfactant is Its foamability is low (for example, cations are added to the mixing tank 10 during the initial mixing operation). Mineral wool and lightweight aggregates are added along with guar gum derivative aggregates. Ionic bonding of wheat starch binder protein via cationic guar on the surface of the membrane. After completely dispersing the mixture and passing the slurry through the head box 3°, the wire belt section 4 The aim is to provide low foaming properties on top of zero and spread it.

本発明に使用するミネラル繊維としては、上述の如(溶融したバサルト、スラグ 、花崗岩等ガラス質ミネラル成分をオリフィスから線状に引き出し繊細化して得 られるいわゆる紡織繊維、または前記の溶融したミネラル成分を紡糸ロータの面 から接線方向に引き出して得られるいわゆるウール繊維、あるいはセラミック繊 維若しくは芳香族ポリアミド繊維等を使用可能である。また本発明によりパネル を作成する際多孔結合マット繊維を個々の繊維として使用し得る。The mineral fibers used in the present invention include those mentioned above (molten basalt, slag , obtained by drawing out glassy mineral components such as granite in a line from an orifice and making them delicate. The so-called textile fibers that are produced, or the molten mineral components mentioned above, are transferred to the surface of the spinning rotor. So-called wool fibers, which are obtained by drawing tangentially from Polyamide fiber or aromatic polyamide fiber can be used. In addition, according to the present invention, the panel The porous bonded mat fibers can be used as individual fibers in making the fibers.

軽量凝集体としてはこれも上述したように剥脱または発泡させたガラス質火山岩 を用いることが好ましく、この凝集体としては、周知の如く各種のメツシュサイ ズのものを得れる発泡パーライト、剥脱ひる石、剥脱クレイ等が挙げられる。As a lightweight aggregate, this is also exfoliated or foamed glassy volcanic rock as mentioned above. It is preferable to use this aggregate, and as is well known, various types of mesh Examples include expanded pearlite, exfoliated vermiculite, and exfoliated clay.

一般に入手性及び経済性の点から発泡パーライトを用いることが好ましい。Generally, it is preferable to use expanded pearlite from the viewpoint of availability and economy.

しかして一部上述したが、均質に混合されイオン結合され僅かに発泡されたスラ リをワイヤベルト部40に沈積させ、ミネラルウール及び軽量凝結体を絡み合わ せ一定で小さな一時的な気孔を少量存在させた多孔構造の組成物を得れる。この 時点では組成物内の気孔の占める割合は組成物の約10〜30容量%であり、残 りは軽量凝結体とミネラル繊維との間に水を含んだ空隙が形成されこの水性スラ リはこの時点では約3〜6固形重星%である。発泡湿潤組成物はヘッドボックス 30から流し部42でワイヤベルト部40上の底部スクリムカバーシート43に 沈積させる。However, as mentioned above, the slurry is homogeneously mixed, ionically bonded, and slightly foamed. The mineral wool and lightweight aggregates are intertwined with each other. A composition with a porous structure in which a small amount of small temporary pores are present can be obtained. this At this point, the proportion of pores in the composition is about 10 to 30% by volume of the composition, and the remaining Water-containing voids are formed between the lightweight aggregate and the mineral fibers, and this aqueous slurry Li is about 3-6% solid double star at this point. Foaming wet composition head box 30 to the bottom scrim cover sheet 43 on the wire belt section 40 at the sink section 42. deposit.

僅かに発泡された組成物からの脱水は、スクリム上部カバーシート47を付加し た上、ローラ36を介し組成物に載置するに伴い高減圧部44において行なう。Dewatering from the slightly foamed composition is accomplished by adding a scrim top cover sheet 47. In addition, as the composition is placed on the composition via the roller 36, it is carried out in the high pressure reduction section 44.

高減圧部44では、約3〜20インチ(0,8〜0.5m )に相応する短いパ ルス態様の圧力により、組成物内の気孔を破壊させ脱水させる。この段階では、 気孔が約1〜3秒間破壊され、脱水液が絡み合った繊維と凝結体スクリムの底部 カバーシートとの接触点に塗布されていることが観察された。In the high decompression section 44, a short pipe corresponding to approximately 3 to 20 inches (0.8 to 0.5 m) is used. The russian pressure destroys the pores within the composition and causes dehydration. At this stage, The pores are destroyed for about 1-3 seconds and the fibers and aggregates are entangled with the dehydrated liquid at the bottom of the scrim. It was observed that it was applied at the contact points with the cover sheet.

高減圧部46及び高減圧部48内でマットに連続的に減圧をかけ同時にマットに 加熱した大量の乾燥空気を高速で通過させることにより空孔を破壊することなく マットを連続的に脱水・乾燥する。両面に不織繊維ガラス・スクリム・カバーシ ートを付着させた構造材用のミネラルパネルを、密度が立方フィート当たり約3 〜10ボンド(50〜160kg/m”) 、好ましくは立方フィート当たり約 3〜6ボンド(50〜1(lokg/m’) 、破壊係数が平方インチ当たり約 60〜120ボンド(42,000〜84.000kg/m3)で、ワイヤベル ト部40上のヘッドボックス30における約3〜6重量%同形分をふくむ組成物 から通し空気により脱水・乾燥させる乾燥器49において得るまでの所要時間は 約10分以下である。このときパネルが高減圧部48を通過した後の水分は約3 %である。熱論パネルは周知の対流乾燥機(図示せず)を用いて通し空気を増加 し約数分間乾燥時間を増大させることにより、更に十分に乾燥出来る。Continuously decompressing the mat in the high decompression section 46 and the high decompression section 48 simultaneously By passing a large amount of heated dry air at high speed, the pores are not destroyed. Continuously dehydrate and dry the mat. Non-woven fiberglass scrim cover on both sides structural mineral panels with a density of about 3 per cubic foot. ~10 Bond (50-160 kg/m”), preferably about 3 to 6 bonds (50 to 1 (lokg/m')) with a rupture coefficient of approximately 60-120 bond (42,000-84,000kg/m3), wire bell Composition comprising about 3-6% by weight of the head box 30 on the head section 40 The time required to obtain the product in the dryer 49, which dehydrates and dries it by passing air, is It takes about 10 minutes or less. At this time, after the panel passes through the high pressure reduction section 48, the moisture content is approximately 3 %. Thermal panels are increased through air using a well-known convection dryer (not shown). By increasing the drying time by about a few minutes, more sufficient drying can be achieved.

上述の構成では、マットを1枚または2枚の不織ガラス繊維スクリムのカバーシ ートと一体形成した。このカバーシートとしては紙、織ガラス繊維、不織ガラス 繊維等の多孔構造のシート材を使用可能である。特に好ましいカッ<−シートと しては、重量が百平方インチ当たり約0.4〜2.5ボンドの不織繊維スクリム が挙げられる。一方性の実施態様として、スクリム上部カバーシート47を除去 し、乾燥器49において脱水・乾燥した後、例えば米国特許第1.769.51 9号、第1.996.033号及び第3.246.063号に開示されるような 粘性を有するバルブをマット上に塗布して、しっくい定木のような好適な装置に より表面に好ましい外観の模様を付す周知の対流乾燥機(図示せず)により全体 を乾燥してもよい。また本発明により得られたパネルに、上部と底部の両スクリ ム・シートをバルブを塗布する前に付すことも出来る。更に下塗り、模様付加け 、保護塗装等の各種仕上げ作業を施すことも可能である。In the configurations described above, the mat is covered with one or two non-woven fiberglass scrim cover sheets. It is integrally formed with the seat. This cover sheet can be paper, woven glass fiber, non-woven glass A porous sheet material such as fiber can be used. Particularly preferable cup<-sheet A non-woven fibrous scrim having a weight of approximately 0.4 to 2.5 bonds per hundred square inches. can be mentioned. As a one-sided embodiment, the scrim top cover sheet 47 is removed. After dehydration and drying in the dryer 49, for example, US Pat. No. 1.769.51 No. 9, No. 1.996.033 and No. 3.246.063. Apply the viscous bulb onto the mat and apply it to a suitable device such as plasterboard. The entire surface is dried using a well-known convection dryer (not shown) which imparts a more desirable appearance to the surface. may be dried. Furthermore, the panel obtained according to the present invention has both top and bottom screen. A damping sheet can also be applied before applying the valve. Further undercoat and pattern addition It is also possible to perform various finishing operations such as protective coating.

以下に本発明の実験例を挙げる。特に指定のない限り、量は全乾量固形分に対す る割合として示される。熱論本発明はこれら実験例に限定するものではないこと は理解されよう。Experimental examples of the present invention are listed below. Amounts are based on total dry solids unless otherwise specified. is expressed as a percentage of Thermal theory The present invention is not limited to these experimental examples. will be understood.

実験例1 カチオン・ビーン・ミール誘導体(グア・2−ヒドロキー3(トリメチルアンモ ニオ)−プロピル・エーテル・クロリド;ヘンケル・コーポレーション(Hen kel Corporation)から販売される商標名GENDRIVE 1 58)を図面に示す補助混合タンク16に水と共に入れ、水溶液を作成した。ミ ネラルウール、発泡パーライト凝結体、ジノニルフェノキシポリ(エチレンショ ン(GAF Che+wicals Corporation)から入手し得る 商標名IGEPAL−DM710)、非イオン・ポリエタノキシ界面活性剤及び CTSボール・クレイを混合タンク10に入れ4秒間混合した。Experimental example 1 Cationic bean meal derivative (guar 2-hydroxy 3 (trimethylammo) (Nio)-propyl ether chloride; Henkel Corporation (Hen Trade name GENDRIVE 1 sold by KEL Corporation 58) was put into the auxiliary mixing tank 16 shown in the drawing together with water to prepare an aqueous solution. Mi neral wool, foamed perlite aggregate, dinonylphenoxy poly(ethylene chloride) Available from GAF Che+wicals Corporation Trade name IGEPAL-DM710), nonionic polyethanoxy surfactant and CTS ball clay was placed in mixing tank 10 and mixed for 4 seconds.

このカチオン・グア誘導体液を混合タンク】0に加えて凝集しヘッドボックス3 0へ送る前に5秒間混合した。固形分に関し、混合タンク10での最終配合では 、ミネラルウールが44,5%、発泡パーライトが29.15%、ホイート・ス ターチが2L 95%(6%残留プロティン分を有しオギルビ・パルス・インコ ーポレーション(Ogilvie Mills Inc、)から販売されている 商標名GENVIS 600テ補助混合タンク16内において190°F(88 ℃)で煮沸したもの) 、CTS−2クレイが1.68%及び約3%同形分分散 液内に非イオン・ポリエタノキシ界面活性剤が1.68%である。この配合物は 混合タンク10からワイヤベルト部40の初段において重力により脱水するヘッ ドボックス30へ送り、スクリム(百平方フィート当たり2.4ボンド(0,1 2kg/m”)のバッテリ形不織ガラス繊維)上に拡布した。高減圧部46での マットは極めて均質にミネラルウール及び軽量凝結体が絡み合わされ、小さな非 弾性の気孔が形成された構造であることが[察された。高減圧部44において水 銀柱で約15インチ(0,4m)に相応する減圧を、極めて短時間(1秒間)パ ルス態様をもって加え、マット内の気孔を直ちに破壊してマットから大量の水を 除去したとき、底部カバーシート43、スクリム上部カバーシート47及び繊維 ・凝結体・クレイの多孔構造コア41からなる湿潤組成物の水分は依然として約 75重量%であった。多孔構造組成物に簡単な脱水を施した上、高減圧部46( 水銀柱で約5インチ(Olm)に相応する減圧を与える)で加熱した大量の乾燥 空気を迅速に組成物に通過させて乾燥し、次いで高減圧部48(組成物の表面に 亙って約14インチ(0,4m)に相応する圧力を与える)及び乾燥器49(組 成物の表面積の平方インチ(0,09m”) ・分光たり約300立方フイート (8,5+a”)概して約50〜350立方7 イー ト(1,4m’〜10m ’) (D通し空気で)において乾燥した。概して、加熱した乾燥空気の温度を 37〜205℃、好ましくは約175℃にする。ヘッドボックス30から通し空 気による乾燥を行う高減圧部48の通過時間は約1/8インチ(0,003m)  〜2インチ(0,05m )のコアの厚さに従い変化させたが、概して約2〜 10分間にせしめた。This cationic guar derivative liquid is added to the mixing tank ] 0 and coagulated into the head box 3. Mixed for 5 seconds before passing to zero. Regarding the solid content, in the final formulation in mixing tank 10, , mineral wool 44.5%, expanded perlite 29.15%, wheat flour Turch is 2L 95% (6% residual protein content, Ogilvie Pulse Parakeet) sold by Ogilvie Mills Inc. Trade name: GENVIS 600T 190°F (88°F) in auxiliary mixing tank 16 ℃), CTS-2 clay is 1.68% and about 3% isomorphic dispersion There is 1.68% nonionic polyethane surfactant in the liquid. This formulation is A head is dehydrated by gravity from the mixing tank 10 at the first stage of the wire belt section 40. Scrim (2.4 bond (0.1 2 kg/m") on a battery type non-woven glass fiber). The mat is extremely homogeneously intertwined with mineral wool and lightweight aggregates, and contains small non-woven materials. It was found that the structure had elastic pores. Water in the high pressure reduction section 44 A vacuum corresponding to approximately 15 inches (0.4 m) is applied to the silver column in a very short period of time (1 second). water is added in a liquid manner, immediately destroying the pores within the mat and drawing large amounts of water out of the mat. When removed, the bottom cover sheet 43, scrim top cover sheet 47 and fibers are removed. - The moisture content of the wet composition consisting of the porous structure core 41 of aggregate/clay is still approximately It was 75% by weight. After simple dehydration of the porous structure composition, the high vacuum section 46 ( drying of large quantities heated to a vacuum corresponding to approximately 5 inches of mercury (Olm) Air is quickly passed through the composition to dry it, and then the high vacuum section 48 (on the surface of the composition) (applying pressure corresponding to approximately 14 inches (0.4 m)) and dryer 49 (assembly). The surface area of the composition is approximately 300 cubic feet per square inch (0.09 m”). (8,5+a”) generally about 50 to 350 cubic feet (1,4 m’ to 10 m ’) (with air passing through D). In general, the temperature of the heated dry air is The temperature is 37-205°C, preferably about 175°C. Empty through head box 30 The passage time through the high vacuum section 48 that performs air drying is approximately 1/8 inch (0,003 m). varied according to core thickness of ~2 inches (0.05 m), but generally approx. I made it last for 10 minutes.

これにより各種の厚さ、密度及び強度特性を有する幾つかのサンプルを作成した 。この場合、コアの平均厚さは0.445〜0.490インチで平均密度は立方 フィート当たり6.3〜7.0ボンドになった。(サンプルパネル面を下にして 行なった)平均破壊係数は平方インチ当たり120ボンドで音響特性テストによ る平均騒音減少率は0.75であった。This produced several samples with various thickness, density and strength properties. . In this case, the average thickness of the core is 0.445 to 0.490 inches and the average density is cubic It came out to be 6.3 to 7.0 bonds per foot. (with the sample panel side down) The average modulus of rupture was 120 bonds per square inch and the acoustic properties were tested. The average noise reduction rate was 0.75.

実験例2 実験例1で用いた成分の一部の量を“半分”、並びに倍にしてパネルサンプルを 作成し一連の評価テストを行った。サンプルの一部では、通し空気による乾燥を 行った後のノくネルサンプルの重量を測定し、次にそのサンプルを対流加熱炉に 入れて一晩乾燥した上、一定型fi(T−A−D処理という)にし絶乾重量と比 較した。下表にその結果を示しである。Experimental example 2 Panel samples were prepared by halving or doubling the amount of some of the ingredients used in Experimental Example 1. We created it and conducted a series of evaluation tests. Some of the samples were dried by passing air. Measure the weight of the drained sample and then place the sample in a convection furnace. After drying overnight, it was made into a constant type fi (referred to as T-A-D treatment) and compared to the absolute dry weight. compared. The table below shows the results.

表から明らかなように、軽量凝結体の量を倍にすると通し空気により乾燥される パネルの水分量が増加される。このサンプルは作成の際粘性が相当に上昇した。As is clear from the table, doubling the amount of lightweight aggregate will allow it to pass through and dry by air. The moisture content of the panel is increased. The viscosity of this sample increased considerably during preparation.

また残留プロティン分を有するホイート・スターチの量を倍にすると、水分も大 幅に増加した。このサンプルも作成の際粘性が相当に上昇した。少量の残留プロ ティンを有するホイート・スターチによりスターチ結合剤を煮沸してもスターチ 結合剤の粘性は上昇せず、この好ましい量の結合剤を用いることにより組成物の 粘性が低く維持され、多孔構造組成物を乾燥空気を通過させて大幅に脱水し乾燥 しうろことは理解されよう。低発泡性の分散剤−界面活性剤の非イオン・ポリエ タノキシレートの!を倍にしても、非弾性の気孔の性質がそれほど変化せず、通 し空気を通過させても気孔がそれほど大幅に破壊されずに脱水され、また脱水中 繊維及び凝結体がそれほど分離されなかった。従来の多くの方法ではパーライト の分離若しくは浮動、スターチあるいはウール繊維の分離若しくは沈下により成 分がかなり屑状になり、脱水の高速化が図れなかった。本発明の重要な点は、残 留プロティンを有するスターチを組み合わせて粘性を増加させない結合剤を用い 、通し空気により脱水されないよう水分を保持させ、僅かに発砲する非イオン・ ポリエタノキシレート分散剤−界面活性剤を用いてカチオン・グア・ガムで結合 されるウールと凝結体とを分散させ、ウールと凝結体が絡み合わされた状態でも 分散させて、通し空気による脱水中でも成分が層状にされることを防止されうろ ことにある。Also, doubling the amount of wheat starch with residual protein content will also increase the moisture content. increased in width. This sample also had a significant increase in viscosity during preparation. small amount of residual pro Wheat starch with tin can be used as a starch binder even when boiled. The viscosity of the binder does not increase and by using this preferred amount of binder the composition The viscosity remains low and the porous structure can be significantly dehydrated and dried by passing dry air through the composition. Shiuroko will be understood. Low foaming dispersant - surfactant nonionic polyester Of tanoxylate! Even if it is doubled, the properties of the inelastic pores do not change much, and the Even when air is passed through, the pores are not significantly destroyed and dehydrated. Fibers and aggregates were not significantly separated. Many traditional methods use perlite. formed by the separation or floating of starch or wool fibers, or by the separation or settling of starch or wool fibers. The water content became quite scrapy, and it was not possible to speed up the dehydration process. The important point of the invention is that the remaining Using a binder that does not increase viscosity by combining starches with distillate proteins , non-ionic foam that retains moisture to prevent dehydration through passing air, and slightly erupts. Polyethanoxylate dispersants - bonded with cationic guar gum using surfactants The wool and aggregates are dispersed, even when the wool and aggregates are entangled. Dispersion prevents ingredients from layering even during dehydration by passing air. There is a particular thing.

以上の説明から、本発明によれば広範囲の密度、特性及び用途を有する構造材用 のミネラルパネル製品の製造法が提供されることは明らかであろう。例えばパネ ルの厚さは約178インチ〜2インチ(0,003〜0.05m)以上に出来る 。且つ希釈ミネラル繊維組成物から密度が立方フィート当たり約3〜約10ポン ド(50〜160kg/m’)の極めて軽量の製品が得られる。From the above description, it can be seen that according to the present invention, the present invention can be used for structural materials having a wide range of densities, properties and uses. It will be clear that a method of manufacturing a mineral panel product is provided. For example, the panel The thickness of the wall can be approximately 178 inches to 2 inches (0,003 to 0.05 m) or more. . and the dilute mineral fiber composition has a density of about 3 to about 10 pounds per cubic foot. An extremely lightweight product of 50 to 160 kg/m' can be obtained.

また従来使用されていた他の成分及び他の補助剤も用途に応じて使用可能である 。例えば、染料、顔料、酸化防止剤、撥水剤、難燃剤殺生剤等を適宜に添加しう る。且つまた本発明のパネルに対し、従来のパネル製造法で採用した切断、トリ ム、成整等の作業、天井格子に対する吊下用のスロット、タブ等の形成作業、仕 上げ・装飾用の表面処理、及び保護塗装作業等も施すことが出来、これは本発明 の技術的思想範囲に含まれる事項である。従来の連続パッチ式パネル形成装置で 使用される、タービンあるいは羽根車を含む各種の構成の混合器あるいは流し部 も併設でき、ヘッドボックスも使用可能である。Other conventionally used ingredients and other adjuvants can also be used depending on the application. . For example, dyes, pigments, antioxidants, water repellents, flame retardants, biocides, etc. should be added as appropriate. Ru. Furthermore, the panels of the present invention are free from the cutting and triangulation methods employed in conventional panel manufacturing methods. work such as finishing, forming slots and tabs for hanging from ceiling grids, etc. It is also possible to perform surface treatments for finishing and decoration, as well as protective coating work, which can be done using the present invention. This is a matter that falls within the scope of technical thought. With conventional continuous patch panel forming equipment Mixers or sinks of various configurations, including turbines or impellers, used A head box can also be used.

西 成分 密度 厚さ 重fi ffンF(kg) 乾燥後 湿度%ポンド/立方フ ィート インチ(1m) 丁−A−D F−重電 の重潰−差(Kg/■3) パーライト含有! サンプル 1 なL 9.20 0.28 0.28 0.22 0.07 3 1.6(147) (0,0071) (0,13) (0,10) (0,3 [+)サンプル 2 14.6% 7.53 0,37 0.26 0.23  0.02 9.90(121) (0,0094) (0,12) (0,10 ) (0,009)サンプル 3 29.2% 6,64 0.46 0.30  0,25 0.85 20.20(+06) (0,012) (0,14)  (0,11) (0,02)サンプル 4 58.3% 5.40 0.62  D、42 0.28 0.14 48.60(86,5) (0,016)  (0,19) (0,13) (0,06)スターチ含有量 サンプル 5 11.5% 6,76 0.49 0,32 0,28 0.0 4 +5.10(10g) (0,012) (0,15) (0,13) ( 0,02)サンプル 6 23.0% 5J9 0,44 0.27 0.22  0.06 25.6(94,3) (0,011) (0,12) (0,1 0) (0,0:’l)サンプル 7 45.9% 5.65 0,42 0, 46 0.20 0.26 132.30(94,4) (0,011) (0 ,21) (0,09) (0,12)グア含有量 サンプル 8 なL 5.83 0.51 0.38 0,25 0.13 5 :1.40(93,4) (0,013) (0,17) (0,11) (0 ,06)サンプル 9 0.04% 5.7B 0.52 0.32 0.25  0.0? 29.00(92,6) (0,0]3) (0,15) (0, 11) (0,03)サンプル 100.08% 6.33 0.49 0.3 3 0.26 0.0g 29.40(101,4) (0,012) (0, 15) (0,12) (0,04)サンプル 110.16% 6.61 0 ,46 0,32 0.25 0.07 28.00(105,9) (0,0 11) (0,15) (0,11) (0,03)非イオン界面活性剤含有量 サンプル 12tlL 5.82 0−50 0.29 0,25 0.04  +7.10(93,2) (0,013) (0,13) (0,1+) (0 ,02)サンプル 130.1114% 6.3I Q、47 0.31 0. 25 0.06 24.30(101) (0,012) (0,14) (0 ,11) (0,03)サンプル 141.68% 6.03 0.50 [1 ,340,250,0935,40(96,6)’(0,013) (0,15 ) (0,11) (0,04)サンプル 153.36% 6.22 0.4 8 0.33 0.25 0.08 33.63(99,6) (0,012)  (0,15) (0,11) (0,04)クレイ含有量 サンプル 16 なt、 5.84 0.52 0.37 G、26 0.11  40.30(93,4) (0,013) (0,17) (0,12) ( 0,05)号ンブk 17 3.36% 6.16 0.49 0.36 0. 25 0.10 40.30(98,7) (0,012) (0,16) < 0.11) (0,05)サンプル 186.72% 6.21 0.50 0 .48 11.28 0.20 71.30(99,5) (0,013) ( 0,22) (0,13) (0,09)国際調査報告West Ingredients Density Thickness Weight fi ff F (kg) After drying Humidity % lb/cubic ft Feet inch (1m) D-A-D F-Heavy electric weight difference (Kg/■3) Contains perlite! Sample 1 L 9.20 0.28 0.28 0.22 0.07 3 1.6 (147) (0,0071) (0,13) (0,10) (0,3 [+) Sample 2 14.6% 7.53 0.37 0.26 0.23 0.02 9.90 (121) (0,0094) (0,12) (0,10 ) (0,009) Sample 3 29.2% 6,64 0.46 0.30 0,25 0.85 20.20 (+06) (0,012) (0,14) (0,11) (0,02) Sample 4 58.3% 5.40 0.62 D, 42 0.28 0.14 48.60 (86,5) (0,016) (0,19) (0,13) (0,06) Starch content Sample 5 11.5% 6,76 0.49 0,32 0,28 0.0 4 +5.10 (10g) (0,012) (0,15) (0,13) ( 0.02) Sample 6 23.0% 5J9 0.44 0.27 0.22 0.06 25.6 (94,3) (0,011) (0,12) (0,1 0) (0,0:’l) Sample 7 45.9% 5.65 0,42 0, 46 0.20 0.26 132.30 (94,4) (0,011) (0 ,21) (0,09) (0,12) Guar content Sample 8 L 5.83 0.51 0.38 0.25 0.13 5 :1.40 (93,4) (0,013) (0,17) (0,11) (0 ,06) Sample 9 0.04% 5.7B 0.52 0.32 0.25 0.0? 29.00 (92,6) (0,0]3) (0,15) (0, 11) (0,03) Sample 100.08% 6.33 0.49 0.3 3 0.26 0.0g 29.40 (101,4) (0,012) (0, 15) (0,12) (0,04) sample 110.16% 6.61 0 ,46 0,32 0.25 0.07 28.00 (105,9) (0,0 11) (0,15) (0,11) (0,03) Nonionic surfactant content Sample 12tlL 5.82 0-50 0.29 0.25 0.04 +7.10 (93,2) (0,013) (0,13) (0,1+) (0 ,02) Sample 130.1114% 6.3IQ, 47 0.31 0. 25 0.06 24.30 (101) (0,012) (0,14) (0 ,11) (0,03) Sample 141.68% 6.03 0.50 [1 ,340,250,0935,40(96,6)'(0,013)(0,15 ) (0,11) (0,04) Sample 153.36% 6.22 0.4 8 0.33 0.25 0.08 33.63 (99,6) (0,012) (0,15) (0,11) (0,04) Clay content Sample 16 t, 5.84 0.52 0.37 G, 26 0.11 40.30 (93,4) (0,013) (0,17) (0,12) ( 0,05) Nbuk 17 3.36% 6.16 0.49 0.36 0. 25 0.10 40.30 (98,7) (0,012) (0,16) < 0.11) (0,05) Sample 186.72% 6.21 0.50 0 .. 48 11.28 0.20 71.30 (99,5) (0,013) ( 0,22) (0,13) (0,09) International search report

Claims (11)

【特許請求の範囲】[Claims] (1)少なくとも1枚の多孔構造の繊維スクリムシートと、ミネラルウールと軽 量凝結体とが絡み合わされ残留プロテインを有する10〜30%のホイート・ス ターチを含んだコアと、少量のカチオン・グア・ビーンと、少量の非イオン・ポ リエタノキシ界面活性剤/分散剤とを備えた構造材用の低密度ミネラルウールパ ネル。(1) At least one porous fiber scrim sheet, mineral wool and light 10-30% wheat flour with residual protein entangled with aggregates. A core containing tart, a small amount of cationic guar bean, and a small amount of non-ionic potassium. Low-density mineral wool foam for structural materials with riethanoxy surfactant/dispersant Nell. (2)第2のスクリムシートを備えてなる特許請求の範囲第1項記載のパネル。(2) The panel according to claim 1, comprising a second scrim sheet. (3)密度が立方フィート当たり3〜10ポンド(約50〜160kg/m3) 、破壊係数が平方インチ当たり少なくとも60ポンド(約42,000kg/m 2)である特許請求の範囲第1項記載のパネル。(3) Density is 3 to 10 pounds per cubic foot (approximately 50 to 160 kg/m3) , with a modulus of rupture of at least 60 pounds per square inch (approximately 42,000 kg/m 2) The panel according to claim 1. (4)0.01〜1%のトリメチルアンモニオプロピル・グア・クロリドを含ん でなる特許請求の範囲第1項記載のパネル。(4) Contains 0.01-1% trimethylammoniopropyl guar chloride A panel according to claim 1 consisting of: (5)分子量が1000で、15エチレン酸化物単位を有する0.01〜3%の 非イオン・ジノリルフェノキシボリル(エタノキ)・エタノールを含んでなる特 許請求の範囲第1項記載のパネル。(5) 0.01-3% with a molecular weight of 1000 and 15 ethylene oxide units A special compound containing non-ionic dinolylphenoxyboryl (ethanol tree) and ethanol. A panel according to claim 1. (6)ミネラルウールと軽量凝結体と煮沸後の粘性が大幅に上昇しない10〜3 0%のスターチと、0.01〜1%のカチオン・グア・ビーンとミネラルウール に対し0.03〜3%の非イオン・ポリエタノキシ界面活性剤/分散剤とからな る希釈水性組成物を作成する工程と、多孔構造の移動支承ワイヤベルト上におい て組成物を移動し繊維と凝結体とが絡み合い水を含んだ気孔と空隙を有する多孔 構造体を作成する工程と、構造体に水銀柱で2〜20インチに相応する減圧を加 えて構造体の空隙を実質的に破壊する事なく気孔を破壊し、構造体を脱水する工 程と、水柱で5〜70インチ(0.13〜1.8m)に相応する圧力を構造体に 加え同時に加熱した乾燥空気を構造体に通過させて実質的に空隙を破壊すること なく構造体を更に脱水し乾燥する工程とを包有してなる移動支承ワイヤベルト上 で構造材用の低密度ミネラルウールパネルを製造する方法。(6) Mineral wool and lightweight aggregates and the viscosity after boiling does not increase significantly 10-3 0% starch and 0.01-1% cationic guar bean and mineral wool and 0.03 to 3% of nonionic polyethanoxy surfactant/dispersant. the process of preparing a diluted aqueous composition and placing it on a moving support wire belt with a porous structure; The fibers and aggregates intertwine to move the composition, forming pores with water-containing pores and voids. The process of creating the structure and applying a vacuum equivalent to 2 to 20 inches of mercury to the structure. A process that destroys pores and dehydrates a structure without substantially destroying the voids in the structure. pressure on the structure corresponding to 5 to 70 inches (0.13 to 1.8 m) in the water column. and simultaneously passing heated dry air through the structure to substantially destroy the voids. A moving support wire belt comprising the steps of further dehydrating and drying the structure without removing water. A method of manufacturing low density mineral wool panels for structural materials. (7)スターチに残留プロテインを有するホイート・スターチを用いてなる特許 請求の範囲第6項記載のパネル製造法。(7) Patent made using wheat starch with residual protein in starch A panel manufacturing method according to claim 6. (8)スターチに約6%の残留プロテインを有するホイート・スターチを用いて なる特許請求の範囲第6項記載のパネル製造法。(8) Using wheat starch with about 6% residual protein in starch A panel manufacturing method according to claim 6. (9)グアにトリメチルアンモニオプロピル・グア・クロリドを用いてなる特許 請求の範囲第6項記載のパネル製造法。(9) Patent for using trimethylammoniopropyl guar chloride in guar A panel manufacturing method according to claim 6. (10)非イオン界面活性剤/分散剤にジノニルフエノキシポリ(エチレノキシ )・エタノールを用いてなる特許請求の範囲第6項記載のパネル製造法。(10) Nonionic surfactant/dispersant: dinonylphenoxy poly(ethylenexy) )・The panel manufacturing method according to claim 6, which uses ethanol. (11)非イオン界面活性剤/分散剤に分子量が約1000で約15のエチレン 酸化物単位を有するジノニルフエノキシポリ(エチレノキシ)・エタノールを用 いてなる特許請求の範囲第6項記載のパネル製造法。(11) Ethylene with a molecular weight of about 1000 and about 15 as a nonionic surfactant/dispersant Using dinonyl phenoxy poly(ethyleneoxy)/ethanol with oxide units A panel manufacturing method according to claim 6, which comprises:
JP63501569A 1987-01-12 1988-01-12 Low density mineral wool panel and its manufacturing method Pending JPH01501859A (en)

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US11255051B2 (en) 2017-11-29 2022-02-22 Kimberly-Clark Worldwide, Inc. Fibrous sheet with improved properties
US11313061B2 (en) 2018-07-25 2022-04-26 Kimberly-Clark Worldwide, Inc. Process for making three-dimensional foam-laid nonwovens
US11591755B2 (en) 2015-11-03 2023-02-28 Kimberly-Clark Worldwide, Inc. Paper tissue with high bulk and low lint

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FR2811662B1 (en) * 2000-07-13 2003-07-18 Saint Gobain Isover THERMAL / PHONIC INSULATION PRODUCT BASED ON MINERAL WOOL
EP2136010A1 (en) * 2008-06-17 2009-12-23 Rockwool International A/S A building system for a building structure
SE2150053A1 (en) * 2021-01-19 2022-07-20 Fibu Ab Method for producing 3d fiber structures

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US1841785A (en) * 1930-06-19 1932-01-19 Cellufoam Corp Method of making layers of distended fibrous materials
US3090699A (en) * 1960-05-12 1963-05-21 Armstrong Cork Co Sag-resistant fiberboard and method of making same
US4062721A (en) * 1976-10-26 1977-12-13 Conwed Corporation Use of surfactant to increase water removal from fibrous web

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Publication number Priority date Publication date Assignee Title
US11591755B2 (en) 2015-11-03 2023-02-28 Kimberly-Clark Worldwide, Inc. Paper tissue with high bulk and low lint
US11255051B2 (en) 2017-11-29 2022-02-22 Kimberly-Clark Worldwide, Inc. Fibrous sheet with improved properties
US11313061B2 (en) 2018-07-25 2022-04-26 Kimberly-Clark Worldwide, Inc. Process for making three-dimensional foam-laid nonwovens
US11788221B2 (en) 2018-07-25 2023-10-17 Kimberly-Clark Worldwide, Inc. Process for making three-dimensional foam-laid nonwovens

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