JPH0672038B2 - Fiber for cement reinforcement - Google Patents
Fiber for cement reinforcementInfo
- Publication number
- JPH0672038B2 JPH0672038B2 JP9367086A JP9367086A JPH0672038B2 JP H0672038 B2 JPH0672038 B2 JP H0672038B2 JP 9367086 A JP9367086 A JP 9367086A JP 9367086 A JP9367086 A JP 9367086A JP H0672038 B2 JPH0672038 B2 JP H0672038B2
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- rubber
- cement
- treatment
- 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.)
- Expired - Lifetime
Links
- 239000004568 cement Substances 0.000 title description 32
- 239000000835 fiber Substances 0.000 title description 26
- 230000002787 reinforcement Effects 0.000 title description 5
- 229920001971 elastomer Polymers 0.000 claims description 24
- 239000005060 rubber Substances 0.000 claims description 24
- 229920005989 resin Polymers 0.000 claims description 19
- 239000011347 resin Substances 0.000 claims description 19
- 229920000126 latex Polymers 0.000 claims description 10
- 229920001187 thermosetting polymer Polymers 0.000 claims description 10
- 239000012783 reinforcing fiber Substances 0.000 claims description 7
- 239000012784 inorganic fiber Substances 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 claims description 3
- 238000000576 coating method Methods 0.000 claims description 3
- 229920000049 Carbon (fiber) Polymers 0.000 description 20
- 239000004917 carbon fiber Substances 0.000 description 20
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 18
- 238000000034 method Methods 0.000 description 16
- 239000000463 material Substances 0.000 description 11
- 239000000243 solution Substances 0.000 description 9
- 238000005452 bending Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000003822 epoxy resin Substances 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 229920000647 polyepoxide Polymers 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 229920003048 styrene butadiene rubber Polymers 0.000 description 5
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
- 238000005470 impregnation Methods 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000004816 latex Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000011159 matrix material Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- -1 polyethylene Polymers 0.000 description 3
- 239000004576 sand Substances 0.000 description 3
- 238000004073 vulcanization Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 238000006703 hydration reaction Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 150000002924 oxiranes Chemical class 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 230000003014 reinforcing effect Effects 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- AOBIOSPNXBMOAT-UHFFFAOYSA-N 2-[2-(oxiran-2-ylmethoxy)ethoxymethyl]oxirane Chemical compound C1OC1COCCOCC1CO1 AOBIOSPNXBMOAT-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000011398 Portland cement Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- 239000012615 aggregate Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000011400 blast furnace cement Substances 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000010556 emulsion polymerization method Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 238000009787 hand lay-up Methods 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 239000011396 hydraulic cement Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 238000013001 point bending Methods 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920003225 polyurethane elastomer Polymers 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920006305 unsaturated polyester Polymers 0.000 description 1
Landscapes
- Reinforced Plastic Materials (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Artificial Filaments (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は繊維強化セメント複合材において、優れた曲げ
強度を有するセメント補強用繊維に関するものである。TECHNICAL FIELD The present invention relates to a fiber for cement reinforcement having excellent bending strength in a fiber-reinforced cement composite material.
近年、セメント系建築材においては、防火性、耐火性、
および耐震性等の要求が一段と厳しさを増しており、そ
れに伴つて、補強用繊維の性能も改良されつつあるが、
従来の繊維を用いた補強法では、未だ十分な性能の改良
は、実現されていない。In recent years, fire resistance, fire resistance,
The demands for earthquake resistance and the like are becoming more severe, and along with that, the performance of the reinforcing fiber is being improved.
In the conventional reinforcing method using fibers, sufficient improvement in performance has not been realized yet.
従来の補強法は、大別して次の2つに分けられる。その
1つは、繊維を所要の長さに切断したチヨツプドストラ
ンドをセメントマトリツクス中に分散させて補強する方
法。また一方は、連続繊維をセメント中に配設して補強
する方法である。The conventional reinforcement methods are roughly classified into the following two. One of them is a method in which a chipped strand obtained by cutting a fiber into a required length is dispersed in cement matrix to reinforce it. The other is a method of reinforcing continuous fibers by arranging them in cement.
しかしながら、従来のいずれの方法においてもセメント
と補強繊維との付着性が悪く、十分な性能が得られない
という問題があつた。However, any of the conventional methods has a problem that the adhesion between the cement and the reinforcing fiber is poor and sufficient performance cannot be obtained.
そこで、本発明者等は従来の問題点を解決すべく鋭意検
討を行なつた結果、補強繊維に特定の組成の被覆層を設
けることによりセメントと補強繊維との付着性が改善さ
れることを見い出し、本発明に到達した。Therefore, as a result of intensive studies to solve the conventional problems, the present inventors have found that the adhesion between the cement and the reinforcing fiber is improved by providing the reinforcing fiber with a coating layer having a specific composition. Found and arrived at the present invention.
すなわち、本発明の目的はセメントと補強繊維との付着
を改良し、優れた曲げ強度を有するセメント補強用繊維
を提供するものである。That is, an object of the present invention is to provide a cement-reinforcing fiber having improved adhesion between cement and reinforcing fiber and having excellent bending strength.
そして、その目的は有機または無機繊維を熱硬化性樹脂
で含浸処理した後、ゴム溶液、またはゴムラテツクスで
被覆し、これを硬化させることによつて得られることを
特徴とするセメント補強用繊維により達成される。And, the object is achieved by a fiber for cement reinforcement characterized by being obtained by impregnating an organic or inorganic fiber with a thermosetting resin, coating it with a rubber solution or a rubber latex, and curing it. To be done.
以下、本発明を説明するに、本発明に用いられる有機ま
たは無機繊維は、特に限定されるものではないが、例え
ば、有機繊維ではナイロン、ポリエステル、レーヨン、
更には、アラミド等の芳香族系繊維が用いられ、無機繊
維では、スチール、ガラス繊維、炭素繊維、および黒鉛
繊維等が用いられる。この内、引張強度150kg/mm2以
上、ヤング率10ton/mm2以上有するものが好ましい。繊
維には、表面処理および仕上剤等により前処理してもよ
い。Hereinafter, to describe the present invention, the organic or inorganic fiber used in the present invention is not particularly limited, for example, as the organic fiber, nylon, polyester, rayon,
Further, aromatic fibers such as aramid are used, and as the inorganic fibers, steel, glass fiber, carbon fiber, graphite fiber and the like are used. Among these, those having a tensile strength of 150 kg / mm 2 or more and a Young's modulus of 10 ton / mm 2 or more are preferable. The fibers may be pretreated with a surface treatment and a finishing agent.
表面処理には気相酸化、液相酸化、または酸化剤等を用
いる方法があり、仕上剤による処理は、集束剤、滑剤、
柔軟仕上剤として用いるエポキシ系、アクリレート系、
ポリエチレン系、ポリブテン系、ポリエステル系、ポリ
ウレタン系、シリコン等の公知の化合物を単独あるいは
併用しても良い。The surface treatment includes gas phase oxidation, liquid phase oxidation, or a method using an oxidizing agent, and the treatment with a finishing agent includes a sizing agent, a lubricant,
Epoxy type, acrylate type, used as a softening agent,
Known compounds such as polyethylene, polybutene, polyester, polyurethane and silicone may be used alone or in combination.
次に、本発明で第一処理に用いる熱硬化性樹脂は、水溶
性、非水溶性にかかわらず、公知のものが用いられる。
例えば、エポキシ化合物、不飽和ポリエステル、ポリイ
ミド類等があり、エチレングリコール、グリセロール、
ソルビドール、プロピレングリコール等の多価アルコー
ル類とエピクロルヒドリンの如きハロゲン含有エポキシ
ド類との反応生成物、およびレゾルシン、ハイドロキノ
ン、ビスフエノールA、カテコール等の多価フエノール
類と前記ハロゲン含有エポキシド類との反応生成物等を
挙げることができる。かかる熱硬化性樹脂は水に溶解、
もしくは乳化分散させた水溶液、あるいは有機溶媒を用
いた溶液として用いられる。Next, as the thermosetting resin used in the first treatment in the present invention, a known one is used regardless of whether it is water-soluble or water-insoluble.
For example, there are epoxy compounds, unsaturated polyester, polyimides, etc., ethylene glycol, glycerol,
Reaction products of polyhydric alcohols such as sorbidol and propylene glycol with halogen-containing epoxides such as epichlorohydrin, and reaction products of polyhydric phenols such as resorcinol, hydroquinone, bisphenol A, and catechol with the halogen-containing epoxides. The thing etc. can be mentioned. Such thermosetting resin is soluble in water,
Alternatively, it is used as an emulsion-dispersed aqueous solution or a solution using an organic solvent.
次に本発明の第二処理で用いられるゴムの種類は、たと
えば、天然ゴム、スチレンブタジエンゴム、アクリロニ
トリルゴム、アクリル酸エステル共重合体、クロロプレ
ンゴム、EPDM、ブチルゴム、クロロスルフオン化ポリエ
チレン、フツ素ゴム、ポリウレタンゴム等の公知のもの
が用いられ、上記のゴム固形物が溶解したサスペンジヨ
ン系で用いるか、あるいは、水エマルジヨン系の乳化重
合法、あるいは他の重合法により得たポリマーを乳化剤
を使用して水エマルジヨン系に再乳化して製造されるラ
テツクスを用いるが、所望のゴム固形分濃度が選択でき
る点でラテツクスを用いる方が好ましい。また、ゴム溶
液、またはゴムラテツクスには、必要によつてフイラー
等の補強材、または加硫剤、および加硫促進剤を混合、
分散させえても良い。Next, the type of rubber used in the second treatment of the present invention includes, for example, natural rubber, styrene butadiene rubber, acrylonitrile rubber, acrylic ester copolymer, chloroprene rubber, EPDM, butyl rubber, chlorosulphonated polyethylene, and fluorine. Known materials such as rubber and polyurethane rubber are used, and they are used in a suspension system in which the above-mentioned rubber solid is dissolved, or a water emulsion emulsion polymerization method, or a polymer obtained by another polymerization method as an emulsifier. A latex prepared by re-emulsifying into a water emulsion system is used, but it is preferable to use the latex because the desired rubber solid content concentration can be selected. Further, the rubber solution or the rubber latex is mixed with a reinforcing material such as a filler, or a vulcanizing agent, and a vulcanization accelerator, if necessary.
It may be dispersed.
繊維に前記第一処理および第二処理を施る方法として、
繊維束または、フイラメントを連続的に引き出し、ロー
ラー等を介して熱硬化性樹脂液の第一浴槽に浸した後、
通常熱処理槽を通して硬化させ、次に、またローラー等
を介して、ゴム溶液、またはゴムラテツクスの第二浴槽
に浸し、熱処理槽を通して硬化させ巻き取る連続含浸処
理法、あるいは、所定の長さに切断した繊維束またはフ
イラメントを前記連続含浸処理法の工程と同じ手順にて
処理を施すバツチ式含浸処理法のいずれを用いてもよ
い。As a method of subjecting the fiber to the first treatment and the second treatment,
After continuously pulling out the fiber bundle or filament and immersing it in the first bath of thermosetting resin liquid via a roller or the like,
Usually, it is cured through a heat treatment tank, and then, through a roller or the like, it is immersed in a rubber solution or a second bath of rubber latices, cured through a heat treatment tank and wound up, or a continuous impregnation treatment, or cut into a predetermined length. Any of the batch-type impregnation treatment methods in which the fiber bundle or filament is treated in the same procedure as the step of the continuous impregnation treatment method may be used.
尚、本発明においては、熱硬化性樹脂による第一処理を
行ない、樹脂が未硬化の状態で引き続き第二処理を行な
うこともできるが、好ましくは少なくとも樹脂が半硬化
状態のものに第二処理を施すことが取扱い等の点から都
合がよい。Incidentally, in the present invention, the first treatment with a thermosetting resin may be carried out, and the second treatment may be carried out continuously in the uncured state of the resin, but it is preferable that at least the resin is in a semi-cured state by the second treatment. It is convenient to apply the above.
その際、熱硬化性樹脂液およびゴム溶液、またはゴムラ
テツクスは、通常、繊維全体を被覆しているが、本発明
の効果を損なわない程度の部分被覆であつても良い。繊
維に対する熱硬化性樹脂の付着量は、50〜200重量%が
好ましい。At that time, the thermosetting resin liquid and the rubber solution or the rubber latex usually coats the entire fiber, but may be a partial coat that does not impair the effects of the present invention. The amount of the thermosetting resin attached to the fibers is preferably 50 to 200% by weight.
樹脂付着量が多すぎると、付着ムラによる凝集破壊が起
こり易く、一方、付着量が少なすぎると繊維本来の引張
強度を生かすことができない。また、繊維に対するゴム
固形分の付着量は、10〜200重量%好ましくは50〜100重
量%で用いるのが良い。ゴム付着量が多すぎると、ゴム
層の凝集破壊が起こり易く、一方、付着量が少なすぎる
と、セメントとの付着が低下する。If the resin adhesion amount is too large, cohesive failure due to uneven adhesion tends to occur, while if the resin adhesion amount is too small, the original tensile strength of the fiber cannot be utilized. The amount of the rubber solid content attached to the fibers is 10 to 200% by weight, preferably 50 to 100% by weight. If the amount of rubber adhered is too large, cohesive failure of the rubber layer tends to occur, while if the amount of rubber adhered is too small, adherence to cement is reduced.
次に被覆した熱硬化性樹脂およびゴムを熱処理して硬化
させる熱処理温度は、第一処理後では通常、70℃以上、
120℃以下で30分程度行う。繊維強度を更に得ようとす
る場合は、150℃以上200℃以下で1時間程度行つても良
い。Next, the heat treatment temperature for heat treating and curing the coated thermosetting resin and rubber is usually 70 ° C. or higher after the first treatment,
Do it for about 30 minutes at 120 ℃ or less. When it is desired to further increase the fiber strength, the heating may be performed at 150 ° C or higher and 200 ° C or lower for about 1 hour.
第二処理後では、100℃以上200℃以下で10〜50分程度行
うのが好ましい。第一処理および第二処理のいずれにお
いても、熱処理温度が低すぎると、樹脂およびゴムが、
十分硬化せず、繊維本来の強度が得られない。一方、熱
処理温度が高すぎると、樹脂およびゴムの変質、劣化が
起こりセメントとの付着が低下する。After the second treatment, it is preferably performed at 100 ° C. or higher and 200 ° C. or lower for about 10 to 50 minutes. In both the first treatment and the second treatment, if the heat treatment temperature is too low, the resin and the rubber are
It does not cure sufficiently and the original strength of the fiber cannot be obtained. On the other hand, if the heat treatment temperature is too high, the resin and rubber are deteriorated and deteriorated, and the adhesion to the cement is reduced.
以上の処理を施した繊維はセメント補強用に用いるに際
し従来技術にあるような繊維形態や施工方法の制限は何
らなく強化セメント材の製法に応じて、短繊維状、長繊
維(ストランド)状、シート状、不織布状、織物状等様
々な形態で使用でき、ダイレクトスプレー法、プレミツ
クス法、含浸法(またはハンドレイアツプ法)、抄造法
等様々な方法で施工できる。When the fiber subjected to the above treatment is used for cement reinforcement, there is no restriction on the fiber form and construction method as in the prior art, depending on the manufacturing method of the reinforced cement material, a short fiber shape, a long fiber (strand) shape, It can be used in various forms such as a sheet form, a non-woven fabric form and a woven form, and can be applied by various methods such as a direct spray method, a premix method, an impregnation method (or a handlay up method) and a papermaking method.
また、ポルトランドセメント、高炉セメント、アルミナ
セメント、ケイ酸カルシウム等の各種水硬性セメントに
配合し板状、管状、柱状等各種形状の繊維強化セメント
材が製造できる。使用すべき繊維の量は、所望の強度特
性を得るように定める。Further, it can be mixed with various hydraulic cements such as Portland cement, blast furnace cement, alumina cement and calcium silicate to produce fiber-reinforced cement materials of various shapes such as plate, tube and column. The amount of fiber to use is determined to obtain the desired strength properties.
通常、セメントの乾燥重量100重量部に対し、0.5〜5重
量部が望ましい。次に、セメントマトリツクスは、セメ
ントと水を混合し水和反応によつて得られるが、水和に
必要な水は、通常、セメントの乾燥重量100重量部に対
し、20〜70重量部、セメント構造体の強度をできるだけ
上げるためには、30〜45重量部の水を混合するのが好ま
しい。さらに、骨材として、砂、ケイ砂等をセメント10
0重量部に対し、50〜200重量部配合する『モルタル』を
用いても良い。Usually, 0.5 to 5 parts by weight is desirable for 100 parts by weight of dry weight of cement. Next, cement matrix is obtained by mixing cement and water by hydration reaction, the water required for hydration is usually 20 to 70 parts by weight, relative to 100 parts by weight of dry weight of cement, In order to increase the strength of the cement structure as much as possible, it is preferable to mix 30 to 45 parts by weight of water. Furthermore, as aggregate, sand, silica sand, etc. are cemented.
You may use "mortar" which mix | blends 50-200 weight part with respect to 0 weight part.
このようにして得られた繊維強化セメント材は、従来の
強化セメント材にない優れた曲げ強度を有することが認
められた。It was confirmed that the fiber-reinforced cement material thus obtained has excellent bending strength, which is not found in conventional reinforced cement materials.
また、本発明の処理を施すことにより、セメントの水お
よびアルカリ性に対して防蝕効果があるため、スチー
ル、ガラス繊維が使用できる利点を持つ。In addition, the treatment of the present invention has an anticorrosion effect against water and alkalinity of cement, and therefore has an advantage that steel and glass fibers can be used.
本発明により、優れた曲げ強度が発現する理由を推察す
ると、熱硬化性樹脂を含浸した繊維の外側にゴム層を被
覆することで、ゴム層が曲げ応力を分散させ、樹脂層の
破壊を防ぐため、繊維の強度が保持され、セメント複合
材として曲げ強度を高める結果になつていると考えられ
る。By inferring the reason why excellent bending strength is exhibited by the present invention, by coating the rubber layer on the outside of the fiber impregnated with the thermosetting resin, the rubber layer disperses the bending stress and prevents the destruction of the resin layer. Therefore, it is considered that the strength of the fiber is maintained and the bending strength of the cement composite is increased.
以下、本発明を実施例により、具体的に説明するが本発
明はその要旨をこえない限り下記の実施例に限定される
ものではない。Hereinafter, the present invention will be specifically described with reference to Examples, but the present invention is not limited to the following Examples unless it exceeds the gist.
(実施例1) 引張強度200kg/cm2、ヤング率40ton/mm2のピツチ系炭素
繊維(長さ30cm)を用い、これを50%濃度のエポキシ樹
脂を含むメチルエチルケトン溶液に含浸し、次いで、80
℃で20分さらに、150℃で20分間乾燥、熱処理を施し樹
脂を硬化させた。続いて、予め、加硫剤および加硫促進
剤を混合、分散させた40%固形分濃度のスチレンブタジ
エンラテツクス(日本ゼオン製)で被覆処理し、次い
で、80℃、20分で乾燥し、さらに、150℃、20分間熱処
理して、ゴムを硬化させた。炭素繊維に対する樹脂、お
よびゴムの付着量は、各々、135重量%、41重量%であ
つた。得られた炭素繊維束を繊維強化セメント材の製造
法であるハンドレイアツプ法の常法に従い、セメント10
0重量部に対し、水55、砂160の各重量部からなるセメン
トマトリツクス中に、一定間隔をもつて張設し、10本の
炭素繊維束を配列させた。続いて、気中養生(温度20
℃、相対湿度65%)し、材令7日で炭素繊維強化セメン
ト材を得た。得られた炭素繊維強化セメント材を下記の
条件で曲げ試験を行なつた。Example 1 Pitch-based carbon fibers having a tensile strength of 200 kg / cm 2 and a Young's modulus of 40 ton / mm 2 (length: 30 cm) were impregnated with a methyl ethyl ketone solution containing a 50% concentration of epoxy resin, and then 80
Further, the resin was cured by being dried at 150 ° C. for 20 minutes and further heat-treated at 150 ° C. for 20 minutes. Subsequently, in advance, a vulcanizing agent and a vulcanization accelerator were mixed and coated with 40% solid content styrene butadiene latex (manufactured by Nippon Zeon Co., Ltd.), followed by drying at 80 ° C. for 20 minutes, Further, the rubber was cured by heat treatment at 150 ° C. for 20 minutes. The amounts of resin and rubber attached to the carbon fibers were 135% by weight and 41% by weight, respectively. The obtained carbon fiber bundle was cemented with a cement 10
Ten carbon fiber bundles were arranged in a cement matrix composed of 55 parts by weight of water and 160 parts by weight of sand with respect to 0 parts by weight at regular intervals. Next, air curing (temperature 20
C., relative humidity 65%), and a carbon fiber reinforced cement material was obtained after 7 days. The obtained carbon fiber reinforced cement material was subjected to a bending test under the following conditions.
試験体寸法;縦32cm、横4cm、厚さ2cm スパン間;26cm かぶり厚;0.3cm 3点曲げ試験法;試験体3枚の平均値その曲げ物性を第
1表に示す。Specimen size: length 32 cm, width 4 cm, thickness 2 cm span span: 26 cm cover thickness: 0.3 cm 3-point bending test method: average value of 3 specimens The bending properties are shown in Table 1.
(実施例2) 実施例1と同一の炭素繊維を用い、2%のエポキシ樹脂
水溶液(ポリエチレングリコール・ジグリシジルエーテ
ル)で前処理を施した。該エポキシ樹脂の付着量は炭素
繊維に対し、約1重量%であつた。(Example 2) Using the same carbon fiber as in Example 1, pretreatment was performed with a 2% aqueous epoxy resin solution (polyethylene glycol diglycidyl ether). The amount of the epoxy resin deposited was about 1% by weight based on the carbon fiber.
以下、実施例1と同様にして得られた炭素繊維強化セメ
ント材の物性を第1表に示した。The physical properties of the carbon fiber reinforced cement material obtained in the same manner as in Example 1 are shown in Table 1 below.
尚、スチレンブタジエンゴムの付着量は炭素繊維に対
し、88重量%であつた。The amount of styrene-butadiene rubber attached was 88% by weight based on the carbon fiber.
(実施例3) 実施例1と同一の炭素繊維を用い、2%のエポキシ樹脂
乳化液(エピクロルヒドリンとビスフエノールAとの反
応生成物に界面活性剤を添加して乳化、分散させた処理
液)で前処理を施した。該エポキシ樹脂の付着量は炭素
繊維に対し、1.5重量%であつた。以下、実施例1と同
様にして得られた炭素繊維強化セメント材の物性を第1
表に示した。(Example 3) Using the same carbon fiber as in Example 1, a 2% epoxy resin emulsion (a treatment liquid obtained by adding a surfactant to the reaction product of epichlorohydrin and bisphenol A to emulsify and disperse it) Was pre-treated with. The amount of the epoxy resin attached was 1.5% by weight based on the carbon fiber. Hereinafter, the physical properties of the carbon fiber-reinforced cement material obtained in the same manner as in Example 1 will be first described.
Shown in the table.
尚、スチレンブタジエンゴムの付着量は炭素繊維に対
し、95重量%であつた。The amount of styrene-butadiene rubber attached was 95% by weight based on the carbon fiber.
(比較例1) 実施例1と同一の炭素繊維を用い、ゴム溶液、またはゴ
ムラテツクスで処理しなかつた以外は、実施例1と同様
にして得られた炭素繊維強化セメント材の物性を第1表
に示した。Comparative Example 1 The physical properties of the carbon fiber reinforced cement material obtained in the same manner as in Example 1 except that the same carbon fiber as in Example 1 was not treated with a rubber solution or a rubber latex are shown in Table 1. It was shown to.
尚、エポキシ樹脂の付着量は炭素繊維に対し、105重量
%であつた。The amount of the epoxy resin attached was 105% by weight based on the carbon fiber.
(比較例2) 実施例1と同一の炭素繊維を用い、ゴム溶液、またはゴ
ムラテツスクに、加硫剤および加硫促進剤を混合、分散
させなかつた以外は、実施例1と同様にして得られた炭
素繊維強化セメント材の物性を第1表に示した。(Comparative Example 2) The same carbon fiber as in Example 1 was used, and was obtained in the same manner as in Example 1 except that the vulcanizing agent and the vulcanization accelerator were not mixed and dispersed in the rubber solution or the rubber latex. The physical properties of the carbon fiber reinforced cement material are shown in Table 1.
尚、エポキシ樹脂および、スチレンブタジエンゴムの付
着量は、炭素繊維に対し、各々、89重量%、76重量%で
あつた。The amounts of the epoxy resin and styrene-butadiene rubber attached were 89% by weight and 76% by weight, respectively, with respect to the carbon fiber.
Claims (1)
浸処理した後、ゴム溶液、またはゴムラテツクスで被覆
し、これを硬化させることによつて得られることを特徴
とするセメント補強用繊維。1. A cement-reinforcing fiber, which is obtained by impregnating an organic or inorganic fiber with a thermosetting resin, coating it with a rubber solution or a rubber latex, and curing it.
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9367086A JPH0672038B2 (en) | 1986-04-23 | 1986-04-23 | Fiber for cement reinforcement |
| EP87105609A EP0242793B1 (en) | 1986-04-23 | 1987-04-15 | Cement reinforcing fiber |
| DE8787105609T DE3784366T2 (en) | 1986-04-23 | 1987-04-15 | REINFORCING FIBER FOR CEMENT. |
| US07/269,070 US4915739A (en) | 1986-04-23 | 1988-11-09 | Modified carbon fiber reinforced cement |
| US07/309,959 US4916012A (en) | 1986-04-23 | 1989-02-09 | Cement reinforcing fiber |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9367086A JPH0672038B2 (en) | 1986-04-23 | 1986-04-23 | Fiber for cement reinforcement |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62252356A JPS62252356A (en) | 1987-11-04 |
| JPH0672038B2 true JPH0672038B2 (en) | 1994-09-14 |
Family
ID=14088836
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9367086A Expired - Lifetime JPH0672038B2 (en) | 1986-04-23 | 1986-04-23 | Fiber for cement reinforcement |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0672038B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US12352661B2 (en) | 2018-04-19 | 2025-07-08 | Kairos Water, Inc. | Leak detection and control system |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5173481B2 (en) * | 2008-02-25 | 2013-04-03 | 須知 晃一 | Recycled waste recycle composite multi-purpose aggregate |
-
1986
- 1986-04-23 JP JP9367086A patent/JPH0672038B2/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US12352661B2 (en) | 2018-04-19 | 2025-07-08 | Kairos Water, Inc. | Leak detection and control system |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62252356A (en) | 1987-11-04 |
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