JPH0238720B2 - - Google Patents
Info
- Publication number
- JPH0238720B2 JPH0238720B2 JP62065954A JP6595487A JPH0238720B2 JP H0238720 B2 JPH0238720 B2 JP H0238720B2 JP 62065954 A JP62065954 A JP 62065954A JP 6595487 A JP6595487 A JP 6595487A JP H0238720 B2 JPH0238720 B2 JP H0238720B2
- Authority
- JP
- Japan
- Prior art keywords
- mineral
- weight
- parts
- sepiolite
- aqueous slurry
- 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.)
- Expired - Lifetime
Links
- 239000011094 fiberboard Substances 0.000 claims description 41
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 41
- 239000011707 mineral Substances 0.000 claims description 41
- 239000002002 slurry Substances 0.000 claims description 34
- 239000004113 Sepiolite Substances 0.000 claims description 28
- 229910052624 sepiolite Inorganic materials 0.000 claims description 28
- 235000019355 sepiolite Nutrition 0.000 claims description 28
- 229960000892 attapulgite Drugs 0.000 claims description 25
- 229910052625 palygorskite Inorganic materials 0.000 claims description 25
- 239000000835 fiber Substances 0.000 claims description 23
- 239000002557 mineral fiber Substances 0.000 claims description 23
- 239000011230 binding agent Substances 0.000 claims description 17
- 238000004519 manufacturing process Methods 0.000 claims description 14
- 239000007787 solid Substances 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 9
- 239000011490 mineral wool Substances 0.000 claims description 8
- 238000001035 drying Methods 0.000 claims description 6
- 239000011491 glass wool Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 description 17
- 230000014759 maintenance of location Effects 0.000 description 14
- 230000000694 effects Effects 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 8
- 238000005452 bending Methods 0.000 description 7
- 229920002678 cellulose Polymers 0.000 description 6
- 239000001913 cellulose Substances 0.000 description 6
- 238000009413 insulation Methods 0.000 description 5
- 239000000123 paper Substances 0.000 description 5
- 238000000465 moulding Methods 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 229920002401 polyacrylamide Polymers 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000010425 asbestos Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000002940 repellent Effects 0.000 description 2
- 239000005871 repellent Substances 0.000 description 2
- 229910052895 riebeckite Inorganic materials 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000001246 colloidal dispersion Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000001723 curing Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000008394 flocculating agent Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 201000005202 lung cancer Diseases 0.000 description 1
- 208000020816 lung neoplasm Diseases 0.000 description 1
- 239000010893 paper waste Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Landscapes
- Paper (AREA)
Description
[産業上の利用分野]
本発明は、岩綿、鉱滓綿、あるいはガラスウー
ルからなる鉱物質繊維を繊維成分とする鉱物質繊
維板の製造方法に関するものであり、不燃性、耐
火断熱性、吸音特性、機械的強度等の諸性能に優
れた性質を奏する鉱物質繊維板を経済的に得る方
法を提供するものである。
[従来の技術]
鉱物質繊維板の製造方法には、鉱物質繊維を適
正量の結合剤や添加剤と共に、10〜100倍に相当
する多量の水中に均一に分散させて水性スラリー
とし、これを抄造、成形した後、乾燥、硬化させ
る湿式抄造法、および鉱物質繊維に適正量の結合
剤や添加剤を添加した混合物に、該混合物の2〜
3倍の水を加え、これをペースト状に練り、押
出、または圧延して板状に成形し、更に乾燥、固
化させるペースト法がある。
[発明が解決しようとする問題点]
前記従来の鉱物質繊維板の製造方法のうちの前
者の湿式抄造法は、量産での生産性に優れている
のが特徴であるが、該方法においては、機械的強
度や硬度等の物理的強度を有する鉱物質繊維板を
得るために、成形用組成物中には一定量の有機質
結合剤が含有されている水性スラリーを使用しな
ければならず、得られる鉱物質繊維板における不
燃性、耐火・断熱性等の防火性能に一定の限界が
存するのが欠点とされている。
また、前記湿式抄造法による鉱物質繊維板の製
造方法においては、使用される水性スラリー中の
有機質および無機質結合剤のリテンシヨン・固着
剤として、良く叩解されているゲル状セルロー
ス、高分子凝集剤、アスベスト等が使用されてい
るが、前記ゲル状セルロースを含有する水性スラ
リーによつて得られる鉱物質繊維板は、リテンシ
ヨン・固着剤たるゲル状セルロースに起因する不
燃性や耐火・断熱性等の防火性能の低下が生ずる
し、また、高分子凝集剤はリテンシヨン・固着剤
としての作用が十分ではなく、更には、アスベス
トはアスベスト粉塵が肺がんの原因となるため、
その使用が制限されているのが実情である。
これに対して本発明の鉱物質繊維板の製造方法
は、不燃性、耐火断熱性、吸音性、機械的強度等
の諸種の性能をバランス良く具備する鉱物質繊維
板を、量産での生産性に優れる湿式抄造法で得る
方法を提供するものである。
[問題点を解決するための手段]
本発明の鉱物質繊維板の製造方法は、岩綿、鉱
滓綿、あるいはガラスウールからなる鉱物質繊維
100重量部と、アタパルジヤイト3〜25重量部と、
繊維長20μ〜2mmのセピオライト0.1〜6重量部と
を必須の固形成分として含有し、かつ前記アタパ
ルジヤイトと繊維長20μ〜2mmのセピオライトと
の重量比が3〜30:1にあり、しかも有機質結合
剤が5重量部以下で有機質成分の合計量が7重量
部以下に抑えられている鉱物質繊維組成物の水性
スラリー、すなわち、前記鉱物質繊維組成物を該
鉱物質繊維組成物の10〜100倍に相当する分量の
水中に前記組成物が略均一に分散されている固形
成分1〜8重量%程度の分散液からなる水性スラ
リーを得る工程と、得られた水性スラリーを、フ
オードリニヤー、丸網型等の抄造機を利用して抄
造、成形する工程と、得られた成形シートを乾
燥、硬化させる工程とからなるものである。
前記構成からなる本発明の鉱物質繊維板の製造
方法において使用される水性スラリー中で主たる
固形成分をなす鉱物質繊維は、岩綿、鉱滓綿、お
よびガラスウールの中から選択されるものであ
る。
また、前記水性スラリーに使用されるアタパル
ジヤイトは、得られる鉱物質繊維板における無機
質結合剤として作用するものであり、同時に、場
合によつて(鉱物質繊維100重量部に対して5重
量部以下の少量の範囲で)添加されることのある
有機質結合剤に対するリテンシヨン・固着剤とし
ての作用をも果すものである。前記鉱物質繊維に
対する無機質結合剤の作用を果すアタパルジヤイ
トは、複鎖構造型粘土で、直径100Å、長さ1〜
数μ程度の針状結晶物で、水中でコロイド状に分
散する性質を有しており、該分散状態での表面積
が210m2/gと極めて大きくなるもので、高度の吸
着性能を具備するものである。
主たる固形成分が鉱物質繊維からなる前記水性
スラリー中に、前記アタパルジヤイトと共に含有
される繊維長20μ〜2mmのセピオライトは、従来
の湿式抄造法による鉱物質繊維板の製造方法で使
用されていた水性スラリーにおける故紙パルプ等
の有機繊維が果していたリテンシヨン、固着作用
を果すものであり、前述のアタパルジヤイトに対
する優れたリテンシヨン、固着作用を奏するもの
である。尚、本発明で使用される繊維長20μ〜2
mmのセピオライトは、繊維長の長い形状を有する
セピオライトを予め選択し、これをパルパーおよ
びフアイナーにより、繊維を短く切断し過ぎない
ようにして解繊することにより、所定の範囲内の
繊維長を有するセピオライトがゲル状で存在して
いるところの水分散性スラリーのかたちで容易に
得られるものである。また、前記鉱物質繊維の水
性スラリーに使用されるセピオライトは繊維長が
20μ未満の短かいものになると、アタパルジヤイ
トに対するリテンシヨン、固着作用が弱くなる
し、また、繊維長が2mmを超える長いものになる
と、水性スラリーの抄造性が悪くなるばかりでな
く、得られる鉱物質繊維板の表面状態が悪くなる
ので、前記使用されるセピオライトはその繊維長
が20μ〜2mmの範囲内のものとされるものであ
る。
前記主たる固形成分が鉱物質繊維からなる水性
スラリー中の一方の必須の固形成分たるアタパル
ジヤイトは、鉱物質繊維100重量部に対して3〜
25重量部の割合で存在するものであるが、これ
は、アタパルジヤイトが3重量部未満の少量にな
ると、アタパルジヤイトによる結合剤の作用が得
られなく、機械的強度に優れた特性を有する鉱物
質繊維板が得られなくなるためであり、また、ア
タパルジヤイトが25重量部を超える過量になる
と、水性スラリーの濾水性が悪く、抄造性が悪く
なるばかりでなく、得られる鉱物質繊維板の撥水
性が低下するためでもある。また、前記水性スラ
リー中の他方の必須の固形成分たる繊維長20μ〜
2mmのセピオライトは、鉱物質繊維100重量部に
対して0.1〜6重量部の割合で存在するものであ
るが、これは、前記セピオライトが0.1重量部未
満の少量になると、前述のアタパルジヤイトに対
するリテンシヨン、固着作用が十分ではなく、優
れた機械的強度を有する鉱物質繊維板が得られな
くなり、また、前記セピオライトが6重量部を超
える大量になると、水性スラリーの濾水性が悪化
して効率の良い抄造を行なうことができなくなる
ためである。
更に、前記鉱物質繊維を主固形成分とする水性
スラリー中における必須の固形成分たる前記アタ
パルジヤイトと繊維長20μ〜2mmのセピオライト
とは、その重量比が3〜30:1の範囲内にあるも
ので、アタパルジヤイト3に対してセピオライト
が1を超えるような場合はセピオライトの過量に
対する不経済が生ずるだけであり、またアタパル
ジヤイト30に対してセピオライトが1未満の場合
には、セピオライトによつて果されるアタパルジ
ヤイトのリテンシヨン作用が十分ではなく、得ら
れる鉱物質繊維板の曲げ強度が低下する等の弊害
が生ずる。
前記鉱物質繊維を主たる固形成分とする水性ス
ラリー中には、必要に応じて、有機質結合剤、結
合助剤、撥水剤等が含有されるが、有機質結合
剤、例えば、パルプ、生澱粉、煮沸澱粉、ポリビ
ニルアルコール、ガーガム、酢酸ビニルエマルジ
ヨン、アクリルエマルジヨン、フエノール樹脂等
の有機質結合剤が、鉱物質繊維100重量部に対し
て5重量部を超えるような場合や、水性スラリー
中の有機質成分の合計量が7重量部を超えるよう
な場合には、得られる鉱物質繊維板の不燃性が低
下し、英国規格による不燃性試験での「non−
combustible」をクリヤーする鉱物質繊維板が得
られ難くなるので、有機質結合剤は5重量部以下
に、また、有機質成分の合計量は7重量部以下に
それぞれ抑えられていることが必要である。な
お、ポリアクリルアミド、ポリアクリルアミド変
性物、硫酸アルミニウム等の結合助剤と、撥水剤
とは、これらの合計量が2重量部以下でその作用
が十分に奏されるものである。
[実施例]
以下、本発明の鉱物質繊維板の製造方法の具体
的な構成を実施例を以つて説明し、併せ、得られ
た鉱物質繊維板の性質を比較のために得られた鉱
物質繊維板と比較して説明する。
実施例1〜6、比較例1〜7
後記第1表の実施例1〜6、比較例1〜7欄に
記載した各組成成分からなる固形成分(1000g)
の4重量%水分散液による水性スラリーを25作
成し、得られた水性スラリーを実験室のテスト抄
造機で抄造、減圧脱水し、次いでプレス機でプレ
ス成形した後、乾燥炉で、170〜250℃、4時間の
乾燥、硬化を行なうことによつて鉱物質繊維板を
得た。
各水性スラリーの成形濾水時間、および得られ
た鉱物質繊維板の密度、曲げ強さ、圧縮強さ、不
燃性を併せて第1表に示す。
なお、第1表中における水性スラリーの成形濾
水時間、抄造工程中におけるリテイン率(%)、
および得られた鉱物質繊維板の各種物性値の測定
方法は以下の通りである。
抄造時濾水時間:各水性スラリーを金網の目の
粗さ50メツシユ、金網部の大きさ400×400、脱水
部の真空度1500mm水柱のテスト抄造機で抄造する
際の濾水時間。
リテイン率:乾燥、硬化後の鉱物質繊維板の重
量を水性スラリー25中に含まれる固形成分重量
で除した値。
曲げ強さ:JIS A5907に従つて測定した値。
圧縮強さ:鉱物質繊維板をその厚さ方向に0.5
mm/分の速度で圧縮し、厚さが85%となつたとき
の応力を面積で除した値。
不燃性:英国規格(BS)476第4部「材料の不
燃性試験」に準じて行なつた値。
[Industrial Field of Application] The present invention relates to a method for producing mineral fiberboard whose fiber component is mineral fiber made of rock wool, mineral wool, or glass wool, and which has properties such as nonflammability, fireproof insulation, and sound absorption. The object of the present invention is to provide a method for economically obtaining mineral fiberboard that exhibits excellent properties such as properties and mechanical strength. [Prior art] The manufacturing method for mineral fiberboard involves uniformly dispersing mineral fibers in a large amount of water equivalent to 10 to 100 times the amount of mineral fibers together with appropriate amounts of binders and additives to form an aqueous slurry. After papermaking and shaping, drying and curing are carried out using a wet papermaking method, and a mixture of mineral fibers and appropriate amounts of binders and additives is added to the mixture.
There is a paste method in which three times as much water is added, the paste is kneaded, extruded or rolled to form a plate, and then dried and solidified. [Problems to be Solved by the Invention] Among the conventional methods for manufacturing mineral fiberboard, the former wet papermaking method is characterized by excellent productivity in mass production. In order to obtain a mineral fiberboard with physical strength such as mechanical strength and hardness, it is necessary to use an aqueous slurry containing a certain amount of an organic binder in the molding composition. A drawback is that there are certain limits to the fireproof performance of the resulting mineral fiberboard, such as nonflammability, fire resistance, and heat insulation. In the method for manufacturing mineral fiberboard by the wet papermaking method, well-beaten gel cellulose, polymer flocculant, Although asbestos and the like are used, the mineral fiberboard obtained from the aqueous slurry containing the gelled cellulose has fireproof properties such as nonflammability, fire resistance, and heat insulation properties due to the gelled cellulose used as a retention and adhesion agent. In addition, polymer flocculants do not have sufficient action as retention/fixing agents, and asbestos dust causes lung cancer.
The reality is that its use is restricted. On the other hand, the method for manufacturing mineral fiberboard of the present invention can produce mineral fiberboard that has various performances such as non-combustibility, fireproof insulation, sound absorption, and mechanical strength in a well-balanced manner, with high productivity and productivity in mass production. The present invention provides a method for obtaining paper using a wet papermaking method with excellent properties. [Means for Solving the Problems] The method for producing a mineral fiberboard of the present invention uses mineral fibers made of rock wool, slag wool, or glass wool.
100 parts by weight, 3 to 25 parts by weight of attapulgite,
It contains 0.1 to 6 parts by weight of sepiolite with a fiber length of 20 μm to 2 mm as an essential solid component, and the weight ratio of the attapulgite to sepiolite with a fiber length of 20 μm to 2 mm is 3 to 30:1, and an organic binder. is 5 parts by weight or less and the total amount of organic components is suppressed to 7 parts by weight or less, that is, the mineral fiber composition is 10 to 100 times the mineral fiber composition. A step of obtaining an aqueous slurry consisting of a dispersion having a solid content of about 1 to 8% by weight, in which the composition is almost uniformly dispersed in an amount of water corresponding to This process consists of a process of papermaking and molding using a papermaking machine such as, etc., and a process of drying and curing the obtained molded sheet. The mineral fibers forming the main solid component in the aqueous slurry used in the method for producing mineral fiberboard of the present invention having the above structure are selected from rock wool, mineral wool, and glass wool. . In addition, the attapulgite used in the aqueous slurry acts as an inorganic binder in the mineral fiberboard obtained, and at the same time, in some cases (up to 5 parts by weight per 100 parts by weight of mineral fibers). It also acts as a retention/fixing agent for organic binders that may be added (in small amounts). Attapulgite, which acts as an inorganic binder for the mineral fibers, is a multi-chain clay with a diameter of 100 Å and a length of 1 to 100 Å.
It is a needle-like crystal substance of several micrometers that has the property of being dispersed in colloidal form in water, and has an extremely large surface area of 210 m 2 /g in the dispersed state, and has a high degree of adsorption performance. It is. The sepiolite with a fiber length of 20μ to 2mm contained together with the attapulgite in the aqueous slurry whose main solid component is mineral fiber is the aqueous slurry used in the conventional method for producing mineral fiberboard by wet papermaking. It performs the retention and fixation effects that organic fibers such as waste paper pulp had in the above-mentioned attapulgite, and provides excellent retention and fixation effects for the above-mentioned attapulgite. In addition, the fiber length used in the present invention is 20 μ to 2
mm sepiolite has a fiber length within a predetermined range by pre-selecting sepiolite with a long fiber length and defibrating it using a pulper and a finer without cutting the fibers too short. It is easily obtained in the form of a water-dispersible slurry in which sepiolite exists in gel form. In addition, the sepiolite used in the mineral fiber aqueous slurry has a fiber length.
If the fiber length is less than 20 μm, the retention and fixing effect on attapulgite will be weakened, and if the fiber length is longer than 2 mm, not only will the paper-formability of the aqueous slurry deteriorate, but the mineral fibers obtained will be Since the surface condition of the plate becomes poor, the fiber length of the sepiolite used is within the range of 20 μm to 2 mm. Attapulgite, which is one essential solid component in the aqueous slurry in which the main solid component is mineral fiber, is present in an amount of 3 to 3 parts by weight per 100 parts by weight of mineral fiber.
It is present in a proportion of 25 parts by weight, but this is because if the amount of attapulgite is less than 3 parts by weight, the binder effect of attapulgite cannot be obtained, and the mineral fiber has excellent mechanical strength. This is because the board cannot be obtained. Furthermore, if the amount of attapulgite exceeds 25 parts by weight, the water-based slurry will not only have poor freeness and paper-making properties, but also the water repellency of the resulting mineral fiberboard will decrease. It is also for the purpose of In addition, the fiber length of the other essential solid component in the aqueous slurry is 20μ~
The 2 mm sepiolite is present in a proportion of 0.1 to 6 parts by weight based on 100 parts by weight of mineral fibers, but this means that if the sepiolite is in a small amount of less than 0.1 part by weight, the retention with respect to the above-mentioned attapulgite, The fixing effect is not sufficient, making it impossible to obtain a mineral fiberboard with excellent mechanical strength. Furthermore, if the amount of sepiolite exceeds 6 parts by weight, the freeness of the aqueous slurry deteriorates, making it difficult to make an efficient paper sheet. This is because they will not be able to do so. Further, the weight ratio of the attapulgite and sepiolite having a fiber length of 20 μm to 2 mm, which are essential solid components in the aqueous slurry having the mineral fiber as the main solid component, is within the range of 3 to 30:1. If the ratio of sepiolite exceeds 1 to 3 parts of attapulgite, there will only be a diseconomie due to the excessive amount of sepiolite, and if the ratio of sepiolite to 30 parts of attapulgite is less than 1, the amount of attapulgite achieved by the sepiolite will increase. The retention effect is not sufficient, causing problems such as a decrease in the bending strength of the resulting mineral fiberboard. The aqueous slurry containing mineral fibers as the main solid component contains an organic binder, a binding aid, a water repellent, etc. as necessary. Organic binders such as pulp, raw starch, When the amount of organic binders such as boiled starch, polyvinyl alcohol, gar gum, vinyl acetate emulsion, acrylic emulsion, and phenolic resin exceeds 5 parts by weight per 100 parts by weight of mineral fibers, or when organic binders are used in aqueous slurry. If the total amount of the ingredients exceeds 7 parts by weight, the non-flammability of the resulting mineral fiberboard will decrease and it will be rated "non-flammable" in the British Standards non-flammability test.
Since it becomes difficult to obtain a mineral fiberboard that clears "combustible", it is necessary to suppress the organic binder to 5 parts by weight or less, and the total amount of organic components to 7 parts by weight or less. Note that the binding aid such as polyacrylamide, polyacrylamide modified product, aluminum sulfate, and water repellent can sufficiently exhibit their effects when the total amount thereof is 2 parts by weight or less. [Example] Hereinafter, the specific structure of the method for producing mineral fiberboard of the present invention will be explained using Examples, and the properties of the obtained mineral fiberboard will be explained using the obtained mineral fiberboard for comparison. This will be explained in comparison with quality fiberboard. Examples 1 to 6, Comparative Examples 1 to 7 Solid components (1000 g) consisting of each composition component listed in the Examples 1 to 6 and Comparative Examples 1 to 7 columns of Table 1 below.
An aqueous slurry with a 4% by weight aqueous dispersion of A mineral fiberboard was obtained by drying and curing at ℃ for 4 hours. Table 1 shows the molding and drainage time of each aqueous slurry, as well as the density, bending strength, compressive strength, and nonflammability of the obtained mineral fiberboard. In addition, the molding drainage time of the aqueous slurry in Table 1, the retention rate (%) during the papermaking process,
The methods for measuring various physical properties of the obtained mineral fiberboard are as follows. Filtration time during papermaking: Filtration time when making each aqueous slurry using a test papermaking machine with a wire mesh coarseness of 50 mesh, a wire mesh section size of 400 x 400, and a vacuum level of 1500 mm water column in the dewatering section. Retention rate: The value obtained by dividing the weight of the mineral fiberboard after drying and curing by the weight of solid components contained in the aqueous slurry 25. Bending strength: Value measured according to JIS A5907. Compressive strength: 0.5 in the thickness direction of mineral fiberboard
The value obtained by compressing at a speed of mm/min and dividing the stress when the thickness reaches 85% by the area. Nonflammability: Values determined in accordance with British Standard (BS) 476 Part 4 "Testing for nonflammability of materials".
【表】
なお、第1表中におけるセピオライトは繊維長
20μ〜2mmの範囲内のものであり、アタパルジヤ
イトもセピオライトも共に、予めパルパーでやわ
らかくほぐした後にリフアイナーにより繊維長が
短くなることのないようにフイブリル化したコロ
イド状分散水液のかたちで使用した。
また、パルプセルロースは、新聞故紙を叩解
し、TAPPI Standard Sheet Machineによる濾
水時間が約400秒のゲル状セルロースとして使用
した。
更に、ポリアクリルアミドは分子量505程度の
ポリマーを使用した。
前記第1表に表示される結果から、実施例にお
ける水性スラリーの濾水性やリテイン率はいずれ
も良好であり、しかも、前記水性スラリーによる
抄造成形体たる鉱物質繊維板は、曲げ強度、不燃
性等においてバランスのとれた良好な物性を有し
ていることが明らかである。
しかしながら、セピオライトを含有しない水性
スラリーを使用する比較例1の場合には、前記セ
ピオライトの作用が得られないために抄造成形工
程でのリテイン率が低く、曲げ強度において満足
される鉱物質繊維板を得ることができない。
過剰のセピオライトを含有する水性スラリーを
使用する比較例2の場合には、得られる鉱物質繊
維板の物性は良好であるが、水性スラリーの濾水
性が悪く、鉱物質繊維板を工業的規模で製造する
には不適当である。
有機質結合剤たるパルプセルロースを過剰に含
有する水性スラリーを使用する比較例5において
は、抄造成形工程でのリテイン率が良く、また得
られた鉱物質繊維板は曲げ強度に優れたものとな
るが、不燃性という面での条件を満足するものは
得られない。
過剰のセピオライトを含有し、しかもアタパル
ジヤイトを含有しない水性スラリーを使用する比
較例6の場合には、前記比較例2の場合と同様に
得られる鉱物質繊維板の物性は良好であるが、水
性スラリーの濾水性が極端に悪くなる。
更に、適量のセピオライトは含有するがアタパ
ルジヤイトを含有しない水性スラリーを使用する
比較例7の場合には、アタパルジヤイトの奏する
結合剤としての作用が得られないため、曲げ強度
や圧縮強度において満足される鉱物質繊維板は得
られない。
[発明の作用および効果]
本発明の鉱物質繊維板の製造方法は、鉱物質繊
維100重量部と、アタパルジヤイト3〜25重量部
と、繊維長20μ〜2mmのセピオライト0.1〜6重量
部とを必須の固形成分として含有し、かつ前記ア
タパルジヤイトと繊維長20μ〜2mmのセピオライ
トとの重量比が3〜30:1にあり、しかも有機質
結合剤が5重量部以下で有機質成分の合計量が7
重量部以下に抑えられている鉱物質繊維組成物の
水性スラリーを、抄造、成形後、乾燥、硬化させ
ることによつて鉱物質繊維板を得るもので、アタ
パルジヤイトの有する無機質結合剤としての作用
と、繊維長20μ〜2mmのセピオライトの有する抄
造成形性に対しての弊害をもたらすことなく奏さ
れる好適なるリテンシヨン作用とを十分に利用し
て鉱物質繊維板を得るものである。
従つて、本発明の鉱物質繊維板の製造方法にお
いては、不燃性、耐火断熱性、吸音性、機械的強
度等の諸性能をバランス良く具備する鉱物質繊維
板を、効率良く、しかも安価、確実に得られると
いう作用、効果が奏されるものである。[Table] In addition, sepiolite in Table 1 is based on the fiber length.
Both attapulgite and sepiolite were used in the form of aqueous colloidal dispersions that were softened with a pulper and then fibrillated with a refiner to prevent shortening of the fiber length. In addition, pulp cellulose was used as a gel-like cellulose obtained by beating waste newspaper and having a drainage time of about 400 seconds using a TAPPI Standard Sheet Machine. Furthermore, the polyacrylamide used was a polymer with a molecular weight of about 505. From the results shown in Table 1 above, the freeness and retention rate of the aqueous slurry in Examples are both good, and the mineral fiberboard, which is a paper-formed product made from the aqueous slurry, has good bending strength and nonflammability. It is clear that it has well-balanced physical properties. However, in the case of Comparative Example 1 in which an aqueous slurry that does not contain sepiolite is used, the retention rate in the paper forming process is low because the effect of sepiolite is not obtained, and a mineral fiberboard with satisfactory bending strength cannot be obtained. can't get it. In the case of Comparative Example 2, in which an aqueous slurry containing an excess of sepiolite is used, the physical properties of the obtained mineral fiberboard are good, but the drainage properties of the aqueous slurry are poor, and the mineral fiberboard cannot be manufactured on an industrial scale. Unsuitable for manufacturing. In Comparative Example 5, in which an aqueous slurry containing an excessive amount of pulp cellulose as an organic binder was used, the retention rate in the paper forming process was good, and the obtained mineral fiberboard had excellent bending strength. However, it is not possible to obtain a material that satisfies the requirements in terms of nonflammability. In the case of Comparative Example 6 in which an aqueous slurry containing excess sepiolite and no attapulgite was used, the physical properties of the mineral fiberboard obtained were good in the same manner as in Comparative Example 2, but the aqueous slurry The freeness of the water becomes extremely poor. Furthermore, in the case of Comparative Example 7, which uses an aqueous slurry that contains an appropriate amount of sepiolite but does not contain attapulgite, attapulgite does not function as a binder, so it cannot be used as a mineral that satisfies the bending strength and compressive strength. quality fiberboard cannot be obtained. [Operations and Effects of the Invention] The method for producing mineral fiberboard of the present invention essentially requires 100 parts by weight of mineral fibers, 3 to 25 parts by weight of attapulgite, and 0.1 to 6 parts by weight of sepiolite with a fiber length of 20 μ to 2 mm. is contained as a solid component, and the weight ratio of the attapulgite to sepiolite with a fiber length of 20 μ to 2 mm is 3 to 30:1, and the organic binder is 5 parts by weight or less and the total amount of organic components is 7:1.
A mineral fiberboard is obtained by paper-forming, forming, drying, and curing an aqueous slurry of a mineral fiber composition that is kept to less than parts by weight. A mineral fiberboard is obtained by making full use of the favorable retention effect of sepiolite having a fiber length of 20 μm to 2 mm, which is exerted without causing any adverse effects on paper forming properties. Therefore, in the method for manufacturing a mineral fiberboard of the present invention, a mineral fiberboard having a well-balanced performance such as non-combustibility, fireproof insulation, sound absorption, and mechanical strength can be produced efficiently and inexpensively. The action and effect that can be achieved reliably are achieved.
Claims (1)
る鉱物質繊維100重量部と、アタパルジヤイト3
〜25重量部と、繊維長20μ〜2mmのセピオライト
0.1〜6重量部とを必須の固形成分として含有し、
かつ前記アタパルジヤイトと繊維長20μ〜2mmの
セピオライトとの重量比が3〜30:1にあり、し
かも有機質結合剤が5重量部以下で有機質成分の
合計量が7重量部以下に抑えられている鉱物質繊
維組成物の水性スラリーを、抄造、成形後、乾
燥、硬化させることを特徴とする鉱物質繊維板の
製造方法。1 100 parts by weight of mineral fibers made of rock wool, slag wool, or glass wool, and attapulgite 3
~25 parts by weight and sepiolite with fiber length of 20μ~2mm
0.1 to 6 parts by weight as an essential solid component,
and a mineral in which the weight ratio of attapulgite to sepiolite with a fiber length of 20 μ to 2 mm is 3 to 30:1, and the organic binder is 5 parts by weight or less and the total amount of organic components is suppressed to 7 parts by weight or less. 1. A method for producing a mineral fiberboard, which comprises paper-forming and forming an aqueous slurry of a quality fiber composition, followed by drying and curing.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6595487A JPS63235600A (en) | 1987-03-20 | 1987-03-20 | Method for manufacturing mineral fiberboard |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6595487A JPS63235600A (en) | 1987-03-20 | 1987-03-20 | Method for manufacturing mineral fiberboard |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63235600A JPS63235600A (en) | 1988-09-30 |
JPH0238720B2 true JPH0238720B2 (en) | 1990-08-31 |
Family
ID=13301885
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6595487A Granted JPS63235600A (en) | 1987-03-20 | 1987-03-20 | Method for manufacturing mineral fiberboard |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63235600A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6461599A (en) * | 1987-08-26 | 1989-03-08 | Nitto Boseki Co Ltd | Mineral fiberboard |
US5679433A (en) * | 1991-10-31 | 1997-10-21 | Kabushiki Kaish Tokiwa Denki | Noncombustible sheet, noncombustible laminated sheet, noncombustible honey comb structural material, noncombustible board, noncombustible molded product, and manufacturing method thereof |
US9174875B2 (en) | 2010-01-07 | 2015-11-03 | Nichias Corporation | Inorganic fibrous molded refractory article, method for producing inorganic fibrous molded refractory article, and inorganic fibrous unshaped refractory composition |
WO2022009845A1 (en) * | 2020-07-10 | 2022-01-13 | 株式会社巴川製紙所 | Flame retardant sheet |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5143485A (en) * | 1974-10-07 | 1976-04-14 | Santo Tekkosho Kk | Koatsu suchiimaano shiiruhohono kairyo |
JPS5747751A (en) * | 1980-09-08 | 1982-03-18 | Nitto Boseki Co Ltd | Manufacture of mineral fiber board |
JPS6021836A (en) * | 1983-07-18 | 1985-02-04 | 株式会社クラレ | Hydraulic inorganic board and manufacture |
-
1987
- 1987-03-20 JP JP6595487A patent/JPS63235600A/en active Granted
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5143485A (en) * | 1974-10-07 | 1976-04-14 | Santo Tekkosho Kk | Koatsu suchiimaano shiiruhohono kairyo |
JPS5747751A (en) * | 1980-09-08 | 1982-03-18 | Nitto Boseki Co Ltd | Manufacture of mineral fiber board |
JPS6021836A (en) * | 1983-07-18 | 1985-02-04 | 株式会社クラレ | Hydraulic inorganic board and manufacture |
Also Published As
Publication number | Publication date |
---|---|
JPS63235600A (en) | 1988-09-30 |
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