JPS6261551B2 - - Google Patents
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- Publication number
- JPS6261551B2 JPS6261551B2 JP8199381A JP8199381A JPS6261551B2 JP S6261551 B2 JPS6261551 B2 JP S6261551B2 JP 8199381 A JP8199381 A JP 8199381A JP 8199381 A JP8199381 A JP 8199381A JP S6261551 B2 JPS6261551 B2 JP S6261551B2
- Authority
- JP
- Japan
- Prior art keywords
- fibers
- weight
- denier
- parts
- impact resistance
- 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
Links
- 239000000835 fiber Substances 0.000 claims description 48
- 239000002994 raw material Substances 0.000 claims description 16
- 239000004760 aramid Substances 0.000 claims description 13
- 229920003235 aromatic polyamide Polymers 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 12
- 239000012210 heat-resistant fiber Substances 0.000 claims description 11
- 229920003002 synthetic resin Polymers 0.000 claims description 10
- 239000000057 synthetic resin Substances 0.000 claims description 10
- 239000010426 asphalt Substances 0.000 claims description 8
- 239000004816 latex Substances 0.000 claims description 8
- 229920000126 latex Polymers 0.000 claims description 8
- 239000000853 adhesive Substances 0.000 claims description 6
- 230000001070 adhesive effect Effects 0.000 claims description 6
- 239000001913 cellulose Substances 0.000 claims description 6
- 229920002678 cellulose Polymers 0.000 claims description 6
- 230000003014 reinforcing effect Effects 0.000 claims description 5
- 239000011381 foam concrete Substances 0.000 claims description 3
- 239000011343 solid material Substances 0.000 claims description 2
- 210000001565 alc Anatomy 0.000 description 19
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 18
- 239000000377 silicon dioxide Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- 239000002002 slurry Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000005187 foaming Methods 0.000 description 4
- 239000003365 glass fiber Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000010425 asbestos Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000004568 cement Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 229910052895 riebeckite Inorganic materials 0.000 description 3
- 239000012756 surface treatment agent Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- 239000011398 Portland cement Substances 0.000 description 2
- 239000002174 Styrene-butadiene Substances 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- -1 etc. Substances 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000004575 stone Substances 0.000 description 2
- 239000011115 styrene butadiene Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- KXJGSNRAQWDDJT-UHFFFAOYSA-N 1-acetyl-5-bromo-2h-indol-3-one Chemical compound BrC1=CC=C2N(C(=O)C)CC(=O)C2=C1 KXJGSNRAQWDDJT-UHFFFAOYSA-N 0.000 description 1
- 229920001651 Cyanoacrylate Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 229920000271 Kevlar® Polymers 0.000 description 1
- 229920003368 Kevlar® 29 Polymers 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- MWCLLHOVUTZFKS-UHFFFAOYSA-N Methyl cyanoacrylate Chemical compound COC(=O)C(=C)C#N MWCLLHOVUTZFKS-UHFFFAOYSA-N 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 229910052782 aluminium Inorganic materials 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
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- 235000012255 calcium oxide Nutrition 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- HNPDNOZNULJJDL-UHFFFAOYSA-N ethyl n-ethenylcarbamate Chemical compound CCOC(=O)NC=C HNPDNOZNULJJDL-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 238000010097 foam moulding Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
- 229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
- 238000009863 impact test Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000004761 kevlar Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- PAZHGORSDKKUPI-UHFFFAOYSA-N lithium metasilicate Chemical compound [Li+].[Li+].[O-][Si]([O-])=O PAZHGORSDKKUPI-UHFFFAOYSA-N 0.000 description 1
- 229910052912 lithium silicate Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920006305 unsaturated polyester Polymers 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Porous Artificial Stone Or Porous Ceramic Products (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Description
本発明は耐衝撃性に優れた水蒸気養生軽量気泡
コンクリート(以下ALCと略称する)に関す
る。
ALCは硅砂、硅石等の硅酸質原料と石灰およ
びセメント等の石灰質原料を粉砕したものに、水
を適当な割合に混合しついでアルミニウム金属物
末等の発泡剤を加えてスラリーとし、これをあら
かじめ補強筋が組込まれた型枠内に鋳込んで発泡
させるか、あるいは型枠内にスラリーを鋳込んで
発泡させた後補強筋を組込み半可塑状となつたも
のをオートクレーブに移して高温高圧水蒸気養生
を行つて製造している。このようにして製造され
たALCは、多数の気孔を有するため水より軽い
という特性を有するが、その製造過程、製品の輸
送又は施工中に受ける衝撃や局部集中荷重等によ
つて欠け易いと言う欠点がある。
建築材料として用いられるこれらALCの欠け
を防止するため従来は、ALCの表層部にガラス
繊維等の繊維物質を合成樹脂系のバインダー等を
用いて接着し補強する方法が提案されている。
しかしながら、これらの繊維物質で上記の補強
をしたものは確かに耐衝撃性を向上させることは
できるが、補強材は極く表層部にのみ固定されて
いるにすぎないため、その効果は期待されるほど
は得られず、さらに耐衝撃性能の向上したものが
切望されているのが現状である。
本願発明者は従来製品の欠点のない、耐衝撃性
の向上したALCを得るため、さきに10デニール
以下のモノフイラメントを20〜15000デニールに
合束した耐熱性の芳香族ポリアミド系の繊維を主
要原料スラリーに混入した製品を発明し特許出願
した(特願昭55−179339)。
本発明の目的は前記のALC製品をさらに改良
した製品を提供することにある。
この目的を達成するため本発明は、ALCの原
料調合物に20デニール以下のモノフイラメントを
単繊維のまゝ又は合束後、合成樹脂、ラテツク
ス、アスフアルト、セルロースのうち1つ以上ま
たはこれらと無機接着剤との混合物を、その付着
量が該繊維1重量部に対し1〜200重量部になる
ように表面処理した耐熱性の芳香族ポリアミド系
の繊維で長さ100mm以下、好ましくは3mm以上100
mm以下の物を前記原料調合物の固形物に対し内割
りで0.1〜3.0重量%添加混合し、のち常法に従つ
てオートクレーブ処理し耐衝撃性に優れたALC
とするものである。
すなわち本発明のALCは、前記芳香族系の耐
熱性繊維のモノフイラメントを合束した後か合束
する前に、合成樹脂、ラテツクス、アスフアル
ト、セルロース又はこれらと無機接着剤とを混合
したものを該繊維1重量部に対し1〜200重量部
付着させてコーテイング処理してから主要原料ス
ラリーに混入する点に新規性を有する。この場合
後者は合成樹脂等を付着させてから所定のデニー
ルに合束する。
上記の繊維を合成樹脂等で表面処理する直接の
目的は、混入させる該繊維のALC製造時の高温
高圧の条件下で原料配合物よりの強アルカリ性物
質の影響による機械的強度の低下防止と、繊維と
ALCの付着力の向上を図ることにあるが、その
結果としてALCの耐衝撃性が向上するものと思
われる。
以下本発明の概要について説明する。
ALCを製造する際に混入させる繊維として
は、本発明で使用する芳香族ポリアミド系の耐熱
性繊維のほかに種々のものが考えられる。例えば
石綿繊維、ガラス繊維又は耐アルカリ性ガラス繊
維、ナイロン、ポリエステル繊維等であるが、石
綿繊維のように“こし”が強く且つ吸水性の強い
繊維は、ALC製造の発泡の過程で独立性のある
球形の気泡形成が阻害され、そのため強度の低下
をきたし耐衝撃性能も低下し、耐アルカリ性ガラ
ス繊維は石綿繊維のように“こし”は強くなく可
撓性に富み良好な発泡性は得られるが、オートク
レーブ養生の過程でアルカリ水に溶出され、また
ナイロン、ポリエステル繊維は耐熱性がないため
オートクレーブ養生過程で溶融してしまう等致命
的な欠点がありこれらはともに好ましくない。従
つて本発明のALC製造に使用される繊維は芳香
族ポリアミド系の耐熱性繊維に特定される。
この繊維の耐熱性としては高温での繊維性能の
保持、寸法の安定性、一定時間暴露後も繊維性能
が保持されること、すなわち高温度雰囲気180℃
以上での荷重伸張曲線が常温状態と殆んど変化し
ないことが必要である。
上記芳香族ポリアミド系の耐熱性繊維として
は、コーネツクス(商品名、帝人社製)ケブラー
29アラミツド(商品名、デユポン社製)、直線配
位性芳香族ポリアミド繊維、例えばポリパラベン
ズアミド等を使用することができる。
次に該繊維の表面処理剤としては、合成樹脂で
はエポキシ、メラミン、フエノール、ユリア、ア
ルキド、不飽和ポリエステル、αオレフイン、ビ
ニールウレタン、ポリウレタン、ポリスチレン、
酢酸ビニール、エチレン酢酸ビニール、アクリル
酢酸ビニール、アクリル、シアノアクリレート、
シリコーン等各樹脂、ラテツクスではクロロプレ
ン、ニトリルゴム、スチレンブタジエンラテツク
ス、天然ラテツクス等、アスフアルトでは天然ア
スフアルト、石油から製造されたストレートアス
フアルト及びブローンアスフアルト等セルロース
ではメチルセルロース、エチルセルロース、シア
ノエチル セルロース、ベンジルセルロース、ハ
イドロキシルメチルセルロース等がある。次に前
記樹脂等と混合して使用し得るものとしては無機
接着剤としてセメント、リン酸アルミニウム、硅
酸ナトリウム、シリカゾル、アルミナゾル、硅酸
リチユーム等一般的な無機接着剤等の単味又はそ
の混合物である。
またこのほかに充填剤として、タルク、炭酸カ
ルシウム、硅石の粉末など、塗料に一般的に添加
されているものを改質のために添加することもで
きる。
次に該繊維の表面処理の方法としては、前記の
合成樹脂、ラテツクス、アスフアルト、セルロー
スのうち1つ以上又はこれらと適当量の無機接着
剤とを混合したものを適正量の有機溶剤又は水で
溶解しあるいはエマルジヨン化し、また場合によ
つては稀釈しないでそのまゝのものを使用し、該
繊維に浸漬法、噴霧法又は塗布法によつてその所
定量を付着させてコーテイングし、ついで風乾、
場合によつては熱処理する一般的な方法を適用す
ることができる。
モノフイラメントの合束は、ごく少量の合成樹
脂等の結束剤を用いるか加縒して合束する。
モノフイラメントを合束したのち、あるいは合
束する前に芳香族ポリアミド系繊維1重量部に対
し1〜200重量部の合成樹脂等を付着させる理由
は、これ以下では前述の該繊維とALCの付着強
度、該繊維の機械的強度が少なく、耐衝撃性の顕
著な効果は認められないからであり、又これ以上
付着させても特に効果の向上が認められないから
である。モノフイラメントを20デニール以下とす
るのはそれ以上の物は製法が困難なためである。
合束された繊維を15000デニール以下とするの
は、これ以上になると合束した繊維の可撓性がな
くなり、発泡時に無理なストレスがかゝり発泡が
阻害され良好な気泡が形成されないためであり、
繊維の長さと繊維の添加量を上記とするのは、繊
維の長さが100mm以上または添加量が3.0重量%以
上の場合には、添加した繊維が相互にからまりあ
つて“まもり”状となり、ために均一な分散が困
難で内部欠陥を生じ機械的強度が低下するためで
あり、繊維の長さが3mm以下または添加量が0.1
重量%以下の場合には耐衝撃性の効果が顕著に現
われないからである。
ALCの主要原料の配合物である石灰者原料と
しては、石灰、セメント等、硅酸質原料としては
硅石、硅砂、高炉スラグ、フライアツシユ等、発
泡剤としてはアルミニウム粉末、界面活性剤等、
補強筋としては鉄、アルミニウム、ステンレス等
の溶接マツト、ラス、金網等一般的に用いられる
ものであれば特に制限されることはない。また原
料配合物の撹拌はパドル型ミキサー、プロペラ型
ミキサー、ターボ型ミキサー、格子型ミキサー、
ポツト型ミキサー等通常使用される撹拌機が使用
できる。尚芳香族ポリアミド系の耐熱性繊維を均
一に分散させる目的で、あらかじめこの繊維に界
面活性剤を施して添加するか、あるいは原料スラ
リーに必要に応じて界面活性剤を添加することも
できる。
発泡成型後のオートクレーブによる蒸気養生
は、例えばゲージ圧10Kg/cm2、温度180℃の飽和
水蒸気による一般的な条件で処理することができ
る。
以下実施例について説明する。
実施例 1
6重量部の生石灰粉末と22重量部のポルトラン
ドセメントと32重量部の硅石粉末と0.05重量部の
アルミニウム粉末と40重量部の水と、前記固形物
の合計量に対し、芳香族ポリアミド系の耐熱性繊
維で1.5デニールのモノフイラメントを加縒法に
より所定の大きさに合束したのち、スチレンブタ
ジエンラテツクスを適当量の水でエマルジヨンと
したものに上記の繊維を浸漬し、その付着量が繊
維1重量部に対し0.5〜250重量部となるように
夫々引揚げ、風乾、熱処理した該繊維を、上記の
スラリーに所定の割合に添加混合して以下通常の
操作に従つて比重0.5のALCを製造した。
得られた製品から10×15×3cmの試験片を切り
取り、耐衝撃試験を行つた。
耐衝撃試験法
試験片を水平に、支点間隔10cmで固定しその中
央部に13cmの高さから300gの茄子型鋼球を落下
させ、試験片にひび割れが生ずるまで繰返し、そ
の落下回数を測定した。
従つて落下回数が多い程耐衝撃性にすぐれてい
ることになる。
また気泡の良否については、顕微鏡観察により
生成した気泡が不均一で独立気泡が少ないものを
否として表現した。また比較例として耐熱性繊維
の表面処理(コーテイング)を行わなかつた繊維
を添加したもの、又は該繊維を全く添加しないも
のについても同様に試験を行つた。
結果を第1表に示す。
芳香族ポリアミド系の耐熱性繊維としてはケブ
ラー29のアラミツド(登録商品名、デユポン社
製)を使用した。
The present invention relates to steam-cured lightweight cellular concrete (hereinafter abbreviated as ALC) with excellent impact resistance. ALC is made by pulverizing silica raw materials such as silica sand and silica stone, and calcareous raw materials such as lime and cement, mixing water in an appropriate ratio, and adding a foaming agent such as aluminum metal powder to form a slurry. Either the slurry is poured into a mold with reinforcing bars installed in advance and foamed, or the slurry is poured into the mold and foamed, then reinforcing bars are incorporated and the semi-plastic state is transferred to an autoclave where it is heated at high temperature and pressure. Manufactured using steam curing. ALC manufactured in this way has a large number of pores, making it lighter than water, but it is said to be prone to chipping due to shocks and local concentrated loads during the manufacturing process, product transportation, or construction. There are drawbacks. In order to prevent these ALCs used as building materials from chipping, a method has conventionally been proposed in which a fibrous material such as glass fiber is bonded to the surface layer of the ALC using a synthetic resin binder for reinforcement. However, although it is true that impact resistance can be improved by reinforcing these fiber materials, the effect is not expected because the reinforcing material is only fixed to the surface layer. At present, it is not possible to obtain as much impact resistance as possible, and there is a strong desire for something with even better impact resistance. In order to obtain ALC with improved impact resistance and without the drawbacks of conventional products, the inventor of the present application first developed a heat-resistant aromatic polyamide fiber, which is made by binding monofilaments of 10 denier or less into 20 to 15,000 denier fibers. He invented a product mixed into raw material slurry and applied for a patent (Japanese Patent Application 179339-1983). An object of the present invention is to provide a product that is further improved from the above-mentioned ALC product. In order to achieve this object, the present invention incorporates monofilaments of 20 denier or less into the raw material composition of ALC, either as single fibers or after bundling, and adding one or more of synthetic resins, latex, asphalt, cellulose, or inorganic fibers with these. A heat-resistant aromatic polyamide fiber whose surface is treated with a mixture with an adhesive so that the adhesion amount is 1 to 200 parts by weight per 1 part by weight of the fiber, and the length is 100 mm or less, preferably 3 mm or more.
ALC with excellent impact resistance is obtained by adding and mixing 0.1 to 3.0% by weight of the solid material of the raw material mixture and then autoclaving it according to a conventional method.
That is. That is, the ALC of the present invention uses synthetic resin, latex, asphalt, cellulose, or a mixture of these and an inorganic adhesive after or before bundling the monofilaments of aromatic heat-resistant fibers. It is novel in that it is applied in an amount of 1 to 200 parts by weight per 1 part by weight of the fibers, coated, and then mixed into the main raw material slurry. In this case, the latter is bonded with a synthetic resin or the like and then bundled to a predetermined denier. The direct purpose of surface-treating the above fibers with synthetic resin etc. is to prevent the mechanical strength from decreasing due to the influence of strong alkaline substances from the raw material mixture under high temperature and high pressure conditions during ALC production of the fibers to be mixed. fiber and
The aim is to improve the adhesion of ALC, and it is thought that the impact resistance of ALC will improve as a result. The outline of the present invention will be explained below. In addition to the aromatic polyamide heat-resistant fiber used in the present invention, various types of fibers may be used to mix in the production of ALC. For example, asbestos fibers, glass fibers, alkali-resistant glass fibers, nylon, polyester fibers, etc., but fibers such as asbestos fibers, which have strong "stiffness" and strong water absorption, are used in the foaming process of ALC production. Formation of spherical bubbles is inhibited, resulting in a decrease in strength and impact resistance.Alkali-resistant glass fibers are not as stiff as asbestos fibers, but are highly flexible and can provide good foaming properties. , they are eluted into alkaline water during the autoclave curing process, and nylon and polyester fibers have fatal disadvantages such as melting during the autoclave curing process due to their lack of heat resistance, and both of these are undesirable. Therefore, the fibers used in the production of ALC of the present invention are specified as heat-resistant aromatic polyamide fibers. The heat resistance of this fiber includes retention of fiber performance at high temperatures, dimensional stability, and retention of fiber performance even after exposure to a high temperature atmosphere of 180℃.
It is necessary that the load-extension curve in the above condition hardly changes from the normal temperature state. The aromatic polyamide-based heat-resistant fibers include Konex (trade name, manufactured by Teijin) and Kevlar.
29 Aramid (trade name, manufactured by DuPont), linear aromatic polyamide fibers, such as polyparabenzamide, etc. can be used. Next, surface treatment agents for the fibers include synthetic resins such as epoxy, melamine, phenol, urea, alkyd, unsaturated polyester, α-olefin, vinyl urethane, polyurethane, polystyrene,
Vinyl acetate, ethylene vinyl acetate, acrylic vinyl acetate, acrylic, cyanoacrylate,
Various resins such as silicone, latex include chloroprene, nitrile rubber, styrene-butadiene latex, natural latex, etc. Asphalt includes natural asphalt, straight asphalt made from petroleum, blown asphalt, etc. Cellulose includes methyl cellulose, ethyl cellulose, cyanoethyl cellulose, benzyl cellulose, hydroxy methylcellulose, etc. Next, examples of inorganic adhesives that can be used in combination with the above resins include common inorganic adhesives such as cement, aluminum phosphate, sodium silicate, silica sol, alumina sol, and lithium silicate, or mixtures thereof. It is. In addition, fillers that are commonly added to paints, such as talc, calcium carbonate, and silica powder, can also be added for modification. Next, as a method for surface treatment of the fibers, one or more of the above-mentioned synthetic resins, latex, asphalt, and cellulose, or a mixture of these and an appropriate amount of inorganic adhesive, is mixed with an appropriate amount of organic solvent or water. Dissolved or emulsionized, or used as is without dilution as the case may be, coated the fiber with a predetermined amount by dipping, spraying, or coating, and then air-drying. ,
In some cases, common methods of heat treatment can be applied. Monofilaments are bundled using a very small amount of binding agent such as synthetic resin or by twisting. The reason for attaching 1 to 200 parts by weight of a synthetic resin, etc. to 1 part by weight of aromatic polyamide fibers after or before bundling the monofilaments is to prevent the adhesion of the above-mentioned fibers and ALC. This is because the strength and mechanical strength of the fibers are low and no significant effect on impact resistance is observed, and no particular improvement in the effect is observed even if the fibers are adhered further. The reason why the monofilament is 20 denier or less is because it is difficult to manufacture monofilaments larger than 20 denier. The reason why the bundled fibers are set to be less than 15,000 denier is because if it exceeds this value, the bundled fibers will lose their flexibility, and excessive stress will be applied during foaming, inhibiting foaming and preventing the formation of good bubbles. can be,
The reason why the length of the fibers and the amount of added fibers are specified above is that if the length of the fibers is 100 mm or more or the amount added is 3.0% by weight or more, the added fibers will become entangled with each other and form a "protective" shape. This is because it is difficult to disperse uniformly, causing internal defects and reducing mechanical strength.
This is because if the amount is less than % by weight, the impact resistance effect will not be noticeable. Limestone raw materials, which are a mixture of the main raw materials for ALC, include lime, cement, etc., silica raw materials include silica stone, silica sand, blast furnace slag, fly ash, etc., and foaming agents include aluminum powder, surfactants, etc.
The reinforcing bars are not particularly limited as long as they are commonly used materials such as welded mats, laths, wire meshes, etc. made of iron, aluminum, stainless steel, etc. In addition, stirring of raw material mixtures can be done using paddle type mixers, propeller type mixers, turbo type mixers, grid type mixers, etc.
A commonly used stirrer such as a pot mixer can be used. In order to uniformly disperse the aromatic polyamide heat-resistant fibers, the fibers may be treated with a surfactant in advance, or a surfactant may be added to the raw material slurry as necessary. Steam curing in an autoclave after foam molding can be carried out under general conditions, for example, using saturated steam at a gauge pressure of 10 Kg/cm 2 and a temperature of 180°C. Examples will be described below. Example 1 6 parts by weight of quicklime powder, 22 parts by weight of Portland cement, 32 parts by weight of silica powder, 0.05 parts by weight of aluminum powder, 40 parts by weight of water, and aromatic polyamide based on the total amount of the solids. After tying 1.5-denier monofilament heat-resistant fibers of the same type into a predetermined size using the twisting method, the fibers were immersed in an emulsion of styrene-butadiene latex with an appropriate amount of water, and its adhesion was confirmed. The fibers were pulled, air-dried, and heat-treated in an amount of 0.5 to 250 parts by weight per 1 part by weight of the fibers, and then added to the above slurry at a predetermined ratio and mixed, followed by a specific gravity of 0.5 according to normal operations. ALC was produced. A test piece measuring 10 x 15 x 3 cm was cut from the obtained product and subjected to an impact test. Impact resistance test method A test piece was fixed horizontally with a fulcrum spacing of 10 cm, and a 300 g eggplant-shaped steel ball was dropped onto the center of the test piece from a height of 13 cm. This was repeated until a crack appeared on the test piece, and the number of drops was measured. Therefore, the greater the number of drops, the better the impact resistance. In addition, regarding the quality of the bubbles, when the bubbles were observed under a microscope and were non-uniform and there were few closed cells, it was expressed as "failure". In addition, as a comparative example, the same tests were carried out using fibers to which heat-resistant fibers were not subjected to surface treatment (coating), or to which the fibers were not added at all. The results are shown in Table 1. Kevlar 29 aramid (registered trade name, manufactured by DuPont) was used as the aromatic polyamide heat-resistant fiber.
【表】【table】
【表】
第1表の結果から耐熱性繊維の長さが〜100mm
で、その添加率が0.1〜3.0重量%の試験例では試
験No.1の繊維無添加の場合に比して耐衝撃性にす
ぐれ気泡状態も良好であつた。そして耐熱性繊維
をラテツクス等で表面処理して、その付着量が該
繊維1重量部に対し1〜200重量部のものは、無
処理の繊維を使用した場合より一段と耐衝撃性の
向上したものが得られた。
本発明製品の範囲を外れた試験No.2、3、8、
9、16、17、32、33は耐衝撃性能が劣り、また試
験No.16、17、32、33は気泡の生成状態が夫々不良
であつた。
実施例 2
実施例1において耐熱性繊維としてコーネツク
ス(商品名、帝人社製)の10デニールのモノフイ
ラメントを、表面処理剤としてフエノール樹脂を
少量のアルコールに溶解したものを使用し、これ
を繊維1重量部に対し25重量部を付着させたの
ち、500デニール、3000デニール、13000デニール
に合束し(繊維の長さは各10mm、30mmおよび100
mmとした)た場合の試験結果は第1表と類似で、
何れも耐衝撃性において充分満足の行く結果が得
られた。
実施例 3
実施例2において、表面処理剤として普通ポル
トランドセメント150重量部および天然ラテツク
スのエマルジヨン10重量部を混合したものに39重
量部の水を添加してよく撹拌したものを使用し、
これを繊維1重量部に対し100、150、200重量部
夫々付着させてコーテイングした場合の試験結果
は第1表と類似で何れも耐衝撃性において充分満
足の行く結果が得られた。[Table] From the results in Table 1, the length of the heat-resistant fiber is ~100mm
In the test examples in which the addition rate was 0.1 to 3.0% by weight, the impact resistance was better and the cell condition was better than in Test No. 1, in which no fiber was added. Heat-resistant fibers that have been surface-treated with latex or the like, with an adhesion amount of 1 to 200 parts by weight per 1 part by weight of the fibers, have much improved impact resistance than when untreated fibers are used. was gotten. Test Nos. 2, 3, and 8, which were outside the scope of the products of the present invention.
Test Nos. 9, 16, 17, 32, and 33 had poor impact resistance, and test Nos. 16, 17, 32, and 33 had poor bubble formation, respectively. Example 2 In Example 1, a 10-denier monofilament of Cornex (trade name, manufactured by Teijin) was used as the heat-resistant fiber, and a phenol resin dissolved in a small amount of alcohol was used as the surface treatment agent. After attaching 25 parts by weight to each part by weight, they are bundled into 500 denier, 3000 denier, and 13000 denier (fiber lengths are 10 mm, 30 mm, and 100 denier, respectively).
The test results when (mm) are similar to Table 1,
In all cases, sufficiently satisfactory results in impact resistance were obtained. Example 3 In Example 2, a mixture of 150 parts by weight of ordinary Portland cement and 10 parts by weight of natural latex emulsion was used as a surface treatment agent, 39 parts by weight of water was added and the mixture was thoroughly stirred.
The test results obtained when 100, 150, and 200 parts by weight of this coating were applied to 1 part by weight of fiber were similar to those shown in Table 1, and in all cases, sufficiently satisfactory results in impact resistance were obtained.
Claims (1)
とし補強筋を内蔵する水蒸気養生軽量気泡コンク
リートにおいて、該原料のスラリー混合物に、20
デニール以下のモノフイラメントを単繊維のまゝ
又は合束後、合成樹脂、ラテツクス、アスフアル
ト、セルロースのうち1つ以上又はこれらと無機
接着剤との混合物によつて、その付着量が繊維1
重量部に対し1〜200重量部となるように表面処
理し15000デニール以下に合束した長さ100mm以下
の芳香族ポリアミド系の耐熱性繊維を、主要原料
の固形物に対して0.1〜3.0重量%混入させて成る
耐衝撃性に優れた水蒸気養生軽量気泡コンクリー
ト。1. In steam-cured lightweight cellular concrete that uses powdered siliceous raw materials and calcareous raw materials as main raw materials and has built-in reinforcing bars, 20%
Monofilaments of denier or less, either as single fibers or after being bundled, are coated with one or more of synthetic resin, latex, asphalt, cellulose, or a mixture of these and an inorganic adhesive, so that the amount of adhesion reaches 1 fiber.
Aromatic polyamide heat-resistant fibers with a length of 100 mm or less, surface-treated to be 1 to 200 parts by weight and bundled to 15,000 denier or less, 0.1 to 3.0 parts by weight to the solid material of the main raw material. % steam-cured lightweight cellular concrete with excellent impact resistance.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8199381A JPS57196754A (en) | 1981-05-28 | 1981-05-28 | Impact-resistant steam-cured lightweight foamed concrete |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8199381A JPS57196754A (en) | 1981-05-28 | 1981-05-28 | Impact-resistant steam-cured lightweight foamed concrete |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57196754A JPS57196754A (en) | 1982-12-02 |
| JPS6261551B2 true JPS6261551B2 (en) | 1987-12-22 |
Family
ID=13761994
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8199381A Granted JPS57196754A (en) | 1981-05-28 | 1981-05-28 | Impact-resistant steam-cured lightweight foamed concrete |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS57196754A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6355239A (en) * | 1986-08-26 | 1988-03-09 | 財団法人鉄道総合技術研究所 | Method for preventing damage due to rat, insect and bacteria in aerated concrete |
-
1981
- 1981-05-28 JP JP8199381A patent/JPS57196754A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57196754A (en) | 1982-12-02 |
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