JP2003055018A - Polymer cement composition - Google Patents
Polymer cement compositionInfo
- Publication number
- JP2003055018A JP2003055018A JP2001246750A JP2001246750A JP2003055018A JP 2003055018 A JP2003055018 A JP 2003055018A JP 2001246750 A JP2001246750 A JP 2001246750A JP 2001246750 A JP2001246750 A JP 2001246750A JP 2003055018 A JP2003055018 A JP 2003055018A
- Authority
- JP
- Japan
- Prior art keywords
- cement
- polymer
- polymer cement
- cement composition
- shrinkage
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000011414 polymer cement Substances 0.000 title claims abstract description 34
- 239000000203 mixture Substances 0.000 title claims abstract description 28
- 239000004568 cement Substances 0.000 claims abstract description 32
- 239000000463 material Substances 0.000 claims abstract description 25
- 229920000642 polymer Polymers 0.000 claims abstract description 17
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 13
- 239000002174 Styrene-butadiene Substances 0.000 claims abstract description 5
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000011115 styrene butadiene Substances 0.000 claims abstract description 5
- 229920003048 styrene butadiene rubber Polymers 0.000 claims abstract description 5
- 229920003051 synthetic elastomer Polymers 0.000 claims abstract description 5
- 239000005061 synthetic rubber Substances 0.000 claims abstract description 5
- 229920001577 copolymer Polymers 0.000 claims abstract description 4
- 229920005989 resin Polymers 0.000 claims description 11
- 239000011347 resin Substances 0.000 claims description 11
- 239000002657 fibrous material Substances 0.000 claims description 9
- 150000002148 esters Chemical class 0.000 claims description 6
- 230000009471 action Effects 0.000 claims description 4
- 229920002125 Sokalan® Polymers 0.000 claims description 3
- 239000004584 polyacrylic acid Substances 0.000 claims description 3
- 239000011435 rock Substances 0.000 abstract description 23
- 238000002347 injection Methods 0.000 abstract description 16
- 239000007924 injection Substances 0.000 abstract description 16
- 238000010276 construction Methods 0.000 abstract description 8
- 238000005336 cracking Methods 0.000 abstract description 5
- 239000004925 Acrylic resin Substances 0.000 abstract description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- 239000000243 solution Substances 0.000 abstract 1
- 230000000694 effects Effects 0.000 description 14
- 239000004815 dispersion polymer Substances 0.000 description 10
- 238000012360 testing method Methods 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000011398 Portland cement Substances 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- 239000000835 fiber Substances 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 238000001035 drying Methods 0.000 description 7
- 239000005038 ethylene vinyl acetate Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 5
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 4
- 238000004898 kneading Methods 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 239000004576 sand Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 235000019738 Limestone Nutrition 0.000 description 2
- XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 239000006004 Quartz sand Substances 0.000 description 2
- 206010040844 Skin exfoliation Diseases 0.000 description 2
- 229920002978 Vinylon Polymers 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 239000010881 fly ash Substances 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000006028 limestone Substances 0.000 description 2
- 229920002239 polyacrylonitrile Polymers 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000008439 repair process Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000008030 superplasticizer Substances 0.000 description 2
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 102100032566 Carbonic anhydrase-related protein 10 Human genes 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 101000867836 Homo sapiens Carbonic anhydrase-related protein 10 Proteins 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001414 amino alcohols Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000011400 blast furnace cement Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000009415 formwork Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920005646 polycarboxylate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000011433 polymer cement mortar Substances 0.000 description 1
- -1 polypropylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229910021487 silica fume Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Landscapes
- Consolidation Of Soil By Introduction Of Solidifying Substances Into Soil (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、特に、山岳部や臨
海部の法面に点在する岩塊のひび割れや間隙等に注入し
て固化させ、岩塊を一体化させることによって岩塊の崩
落等を防止する岩ひび割れ注入材として好適に使用する
ことができるポリマーセメント組成物に関するものであ
る。TECHNICAL FIELD The present invention particularly relates to the formation of rock masses by injecting into the cracks or gaps of rock masses scattered on the slopes of mountainous areas and coastal areas to solidify them and to integrate the rock masses. The present invention relates to a polymer cement composition which can be suitably used as a rock crack injection material for preventing collapse and the like.
【0002】[0002]
【従来の技術】山岳部や臨海部の法面に点在する岩塊に
は、ひび割れや間隙が生じている場合があり、これを放
置すると降雨や地震などの際にその岩塊が崩落する危険
性があり、このような岩塊の崩落を有効に防止すること
が望まれている。2. Description of the Related Art Rock masses scattered on the slopes of mountainous areas and coastal areas may have cracks and gaps, and if left unattended, the rock masses will collapse during rainfall or earthquakes. There is a risk, and it is desired to effectively prevent such collapse of rock mass.
【0003】そこで従来、このような岩塊の崩落を防止
すべく、岩塊のひび割れや岩塊同士の間隙にポリマーセ
メント系注入材を注入する方法が知られいる。そして、
この種のポリマーセメント系注入材としては、エチレン
酢酸ビニル樹脂系ポリマーディスパージョンを用いたも
のが知られている。Therefore, conventionally, in order to prevent such collapse of rock mass, there is known a method of injecting a polymer cement type injection material into cracks of rock mass and gaps between rock masses. And
As this type of polymer cement-based injecting material, one using an ethylene vinyl acetate resin-based polymer dispersion is known.
【0004】[0004]
【発明が解決しようとする課題】しかしながら、エチレ
ン酢酸ビニル樹脂系ポリマーディスパージョンを用いた
ポリマーセメント系注入材は、該ポリマー自体が耐水性
に劣る為、十分に乾燥させた後であっても水に接触する
とポリマーが再溶解するという問題がある。また、該ポ
リマー自体の粘性が高いため、所定の作業性や注入性を
確保するために混練水量を増やさざるを得ず、結果とし
て硬化体組織の緻密性が損なわれ、強度低下や耐水性の
低下を招くという問題がある。さらに、エチレン酢酸ビ
ニル樹脂系ポリマー自体の分子構造にはセメントの水和
反応を遅延させる官能基が存在し、ポリマーセメント系
注入材の硬化および強度発現が阻害されるという問題が
ある。However, since the polymer itself is poor in water resistance, the polymer cement injecting material using the ethylene vinyl acetate resin-based polymer dispersion has a poor water resistance even after being sufficiently dried. There is a problem that the polymer is redissolved when contacted with. Further, since the viscosity of the polymer itself is high, the amount of kneading water has to be increased in order to ensure the predetermined workability and pouring property, and as a result, the denseness of the cured body structure is impaired, and the strength is reduced and There is a problem of causing a decrease. Further, there is a problem that the ethylene vinyl acetate resin-based polymer itself has a functional group in the molecular structure that delays the hydration reaction of the cement, which hinders the hardening and strength development of the polymer-cement-based injection material.
【0005】一方、上記以外のポリマーセメント系注入
材として、ポリアクリル酸エステル樹脂系、スチレンブ
タジエン合成ゴム系、エチレン酢酸ビニル系、又は酢酸
ビニルベオバアクリル共重合系のポリマーディスパージ
ョンを用いたものがある。ポリアクリル酸エステル樹脂
系等のポリマーディスパージョンを用いたセメント系注
入材は、耐水性に優れ且つポリマーの分子構造によって
セメントの強度発現が阻害されることがないので、上述
したような問題が生じる虞がない。On the other hand, as a polymer cement-based injecting material other than the above, one using a polyacrylic ester resin-based, styrene-butadiene synthetic rubber-based, ethylene vinyl acetate-based, or vinyl acetate-vaoba acrylic copolymer-based polymer dispersion There is. Cement-based injecting materials using polymer dispersions such as polyacrylic acid ester resin have excellent water resistance and the molecular structure of the polymer does not hinder the strength development of the cement, thus causing the above-mentioned problems. There is no fear.
【0006】しかしながら、ポリアクリル酸エステル樹
脂ポリマーディスパージョンを用いた場合には、強度発
現性に優れるが故に、硬化の初期に樹脂が皮ばりを起こ
し、さらに直射日光や通風過多などにより急激な乾燥を
受ける場合には、完全硬化するまでに硬化体表面に所謂
プラスチックひび割れを生じるという問題がある。However, when the polyacrylic ester resin polymer dispersion is used, the resin exhibits skin peeling at the initial stage of curing due to its excellent strength development property, and the resin is rapidly dried due to direct sunlight or excessive ventilation. In the case of receiving the above-mentioned problem, there is a problem that so-called plastic cracks are formed on the surface of the cured product before the complete curing.
【0007】また、前記いずれのポリマーセメント系注
入材においても、セメントの乾燥収縮を完全に抑制する
のは困難であり、2〜3週間から1〜2ヶ月後にかけて
セメントの乾燥収縮に起因すると思われるひび割れの発
生が見られることもある。このような乾燥収縮によるひ
び割れが発生すると、岩塊の接着作用が低下し、注入材
本来の機能を低下させる虞がある。Further, it is difficult to completely suppress the drying shrinkage of the cement in any of the above-mentioned polymer cement type injection materials, and it is considered that the drying shrinkage of the cement is caused after 2-3 weeks to 1-2 months. Occurrence of cracks may also be seen. If cracks are generated due to such drying shrinkage, the adhesive action of the rock mass is reduced, and the original function of the injection material may be reduced.
【0008】本発明は、このような従来技術の問題点に
鑑み、施工直後および施工後数ヶ月経過した後にも施工
面にひび割れを発生させることのない、安定した岩塊接
着能を有するポリマーセメント系注入材を提供すること
を課題とする。In view of the above problems of the prior art, the present invention is a polymer cement having a stable rock mass adhering ability, which does not cause cracks on the construction surface immediately after construction and even after several months after construction. An object is to provide a system injection material.
【0009】[0009]
【課題を解決するための手段】本発明は、このような課
題を解決するためになされたものであり、その解決手段
は、セメントと、ポリアクリル酸エステル樹脂系、スチ
レンブタジエン合成ゴム系、又は酢酸ビニルベオバアク
リル共重合系のうち少なくとも1種のポリマーと、界面
活性作用を有する有機系の収縮低減剤とを含有してなる
ことを特徴とするポリマーセメント組成物にある。The present invention has been made to solve the above problems, and the means for solving the problems are cement, polyacrylic ester resin system, styrene butadiene synthetic rubber system, or There is provided a polymer cement composition comprising at least one polymer selected from vinyl acetate vinyl acetate copolymers and an organic shrinkage reducing agent having a surface active action.
【0010】かかるポリマーセメント組成物によれば、
有機系の収縮低減剤の主成分であるポリエチレングリコ
ール、ポリプロピレングリコール、ポリエーテル、ある
いはそれらの誘導体化合物等が、その収縮低減剤の本来
の作用効果を発揮することによりセメントの乾燥収縮を
防止する。さらに、該収縮低減剤によって、セメントの
乾燥収縮を抑制するだけでなく、その界面活性作用によ
って硬化過程の初期におけるポリアクリル酸エステル樹
脂による皮ばりを有効に防止し、初期の硬化過程におけ
る所謂プラスチックひび割れの発生を抑制するという予
期せぬ効果を奏することができる。According to such a polymer cement composition,
Polyethylene glycol, polypropylene glycol, polyether, or their derivative compounds, which are the main components of the organic shrinkage-reducing agent, prevent the cement from drying and shrinking by exhibiting the original function and effect of the shrinkage-reducing agent. Furthermore, the shrinkage-reducing agent not only suppresses the drying shrinkage of cement, but also effectively prevents skinning due to the polyacrylate resin in the initial stage of the curing process due to its surface-active effect, so-called plastic in the initial curing process. An unexpected effect of suppressing the occurrence of cracks can be achieved.
【0011】また、本発明は、前記ポリマーセメント組
成物において、さらに繊維材料が含有してなるものにあ
る。繊維材料が含まれている場合には、該繊維材料によ
っても乾燥収縮応力を分散させることができ、前記収縮
低減剤と繊維材料との双方が相乗的に作用することよっ
て極めて有効に乾燥収縮によるひび割れを抑制すること
が可能となる。Further, the present invention is the above-mentioned polymer cement composition, which further comprises a fiber material. When the fiber material is contained, the dry shrinkage stress can be dispersed also by the fiber material, and both the shrinkage reducing agent and the fiber material act synergistically, so that the dry shrinkage can be effectively performed. It is possible to suppress cracking.
【0012】また、本発明の手段は、前記ポリマーセメ
ント組成物において、さらに膨張材が含有してなるもの
にある。膨張材が含まれている場合には、前記乾燥収縮
の低減がより顕著となり、乾燥収縮によるひび割れをよ
り効果的に防止することが可能となる。The means of the present invention is that the polymer cement composition further comprises an expanding material. When the expansive material is contained, the reduction of the dry shrinkage becomes more remarkable, and the crack due to the dry shrinkage can be more effectively prevented.
【0013】[0013]
【発明の実施の形態】以下、本発明に係るポリマーセメ
ント組成物について、より詳細に説明する。BEST MODE FOR CARRYING OUT THE INVENTION The polymer cement composition according to the present invention will be described in more detail below.
【0014】本発明において使用するポリマーとして
は、ポリアクリル酸エステル樹脂系、スチレンブタジエ
ン合成ゴム系、又は酢酸ビニルベオバアクリル共重合系
のうち、少なくとも1種を使用することができる。ま
た、該ポリマーは、その使用形態については限定されな
い。従って、例えばディスパージョン状態となったもの
を現場において施工直前に混合するものや、該ポリマー
を再乳化型の粉末として予めセメント等と混合してお
き、水を添加して混練する際にディスパージョン状態と
なるものなど、いずれの形態でも使用することができ
る。As the polymer used in the present invention, at least one selected from the group consisting of polyacrylic acid ester resin, styrene-butadiene synthetic rubber, and vinyl acetate vinyl acrylate copolymer can be used. The usage form of the polymer is not limited. Therefore, for example, the one that is in the dispersion state is mixed at the site immediately before construction, or the polymer is mixed in advance as a re-emulsifying powder with cement or the like, and the dispersion is added when kneading by adding water. It can be used in any form such as a state.
【0015】該ポリマーの配合割合は、セメント100
重量部に対して、3〜30重量部となるようにすること
が好ましい。3重量部より少なければ、岩塊との付着強
度の改善や粘度増加を抑制する効果が不十分であり、3
0重量部より多くしてもそれ以上の効果を得られず、か
えってコスト高となる。The blending ratio of the polymer is 100% cement.
The amount is preferably 3 to 30 parts by weight with respect to parts by weight. If the amount is less than 3 parts by weight, the effect of improving the adhesion strength with the rock mass and suppressing the increase in viscosity is insufficient.
Even if the amount is more than 0 parts by weight, no further effect can be obtained and the cost is rather increased.
【0016】また、収縮低減剤としては、アルコール
系、低級アルコールアルキレンオキシド誘導体系、グリ
コール系、グリコールエーテル・アミノアルコール誘導
体系、ポリエーテル系などの界面活性作用を有する有機
系の化合物を使用することができる。これらの収縮低減
剤は、未反応水分の逸散を防止してセメント水和物の乾
燥収縮を抑制するという効果を発揮する。さらに、どの
ような作用によるものかは、解明されていないが、ポリ
マーの皮ばりを防止する効果を発揮するものである。従
って、該収縮低減剤を添加することにより、セメントお
よびポリマーの双方に起因する収縮現象およびひび割れ
の発生を効果的に防止することが可能となる。収縮低減
剤の配合割合としては、セメント100重量部に対し
て、0.3〜6重量部となるようにすることが好まし
い。0.3重量部より少なければ改善効果が不十分であ
り、6重量部より多くしても、それ以上の改善効果が得
られずにかえってコスト高となる。As the shrinkage-reducing agent, use should be made of alcohol-based, lower alcohol alkylene oxide-derivative-based, glycol-based, glycol ether / amino alcohol derivative-based, polyether-based organic compounds having a surface-active action. You can These shrinkage reducing agents exhibit the effect of preventing the unreacted water from escaping and suppressing the dry shrinkage of the cement hydrate. Furthermore, although it has not been clarified what kind of action it causes, it exerts an effect of preventing skin peeling of the polymer. Therefore, by adding the shrinkage reducing agent, it becomes possible to effectively prevent the shrinkage phenomenon and the occurrence of cracks due to both the cement and the polymer. The content of the shrinkage reducing agent is preferably 0.3 to 6 parts by weight with respect to 100 parts by weight of cement. If it is less than 0.3 parts by weight, the improvement effect is insufficient, and if it is more than 6 parts by weight, no further improvement effect is obtained and the cost is rather increased.
【0017】また、本発明における繊維材料としては、
ポリビニルアルコール(ビニロン)繊維、ポリアミド繊
維、ポリエステル繊維、ポリプロピレン繊維、ポリアク
リロニトリル繊維、アラミド繊維、炭素繊維および耐ア
ルカリガラス繊維などを使用することができる。かかる
繊維材料が岩ひび割れ注入剤に含まれている場合には、
収縮応力を分散させてひび割れの発生を抑制することが
できる。中でも、ポリビニルアルコール繊維、ポリアミ
ド繊維、ポリアクリロニトリル繊維および耐アルカリガ
ラス繊維は、セメント水和物との化学的結合による極め
て優れた付着性を有するものであるため、より好適に使
用することができる。Further, as the fiber material in the present invention,
Polyvinyl alcohol (vinylon) fibers, polyamide fibers, polyester fibers, polypropylene fibers, polyacrylonitrile fibers, aramid fibers, carbon fibers, alkali-resistant glass fibers and the like can be used. When such fibrous material is included in the rock crack injecting agent,
It is possible to disperse the shrinkage stress and suppress the occurrence of cracks. Among them, polyvinyl alcohol fibers, polyamide fibers, polyacrylonitrile fibers, and alkali-resistant glass fibers can be used more preferably because they have extremely excellent adhesiveness due to chemical bonding with cement hydrate.
【0018】繊維材料の配合割合としては、セメント1
00重量部に対して、0.1〜1重量部となるようにす
ることが好ましい。0.1重量部より少なければ前記ひ
び割れ抑制効果が不十分であり、1重量部より多くして
も、それ以上の効果が得られずにかえってコスト高とな
る。Cement 1 is used as the mixing ratio of the fiber material.
It is preferable that the amount is 0.1 to 1 part by weight with respect to 00 parts by weight. If the amount is less than 0.1 part by weight, the effect of suppressing cracking is insufficient, and if the amount is more than 1 part by weight, no further effect is obtained and the cost is rather increased.
【0019】また、セメントとしては、普通ポルトラン
ドセメント、早強ポルトランドセメント、超早強ポルト
ランドセメント、耐硫酸塩ポルトランドセメント、中庸
熱ポルトランドセメント、低熱ポルトランドセメント等
の各種ポルトランドセメントや、高炉セメント、フライ
アッシュセメント、シリカセメント等の各種混合セメン
ト、または前記ポルトランドセメントに高炉スラグ微粉
末、フライアッシュ、シリカヒューム、石灰石粉等の混
和材を添加したセメントを使用することができる。As the cement, various Portland cements such as normal Portland cement, early strength Portland cement, super early strength Portland cement, sulfate resistant Portland cement, moderate heat Portland cement, low heat Portland cement, blast furnace cement and fly ash. It is possible to use various mixed cements such as cement and silica cement, or cement in which admixtures such as blast furnace slag fine powder, fly ash, silica fume, and limestone powder are added to the Portland cement.
【0020】また、本発明のポリマーセメント組成物に
は、前記各成分の効果を妨げない範囲において細骨材を
添加することが好ましく、該細骨材としては、川砂、山
砂、海砂、砕砂、石灰岩砂、寒水石などを使用すること
ができる。該細骨材の配合割合は、前記セメント100
重量部に対して30〜300重量部の範囲とすることが
好ましい。該範囲外であれば、注入材のフレッシュ時の
作業性が悪化したり、或いは硬化後の物性が著しく変わ
ってしまい、良好な注入材を得ることが困難となる。Further, it is preferable to add fine aggregate to the polymer cement composition of the present invention within a range that does not impair the effects of the above-mentioned respective components. Examples of the fine aggregate include river sand, mountain sand, sea sand, Crushed sand, limestone sand, cold water stone, etc. can be used. The mixing ratio of the fine aggregate is 100% of the cement.
The amount is preferably in the range of 30 to 300 parts by weight with respect to parts by weight. If it is out of this range, the workability of the injection material at the time of freshness is deteriorated or the physical properties after curing are significantly changed, and it becomes difficult to obtain a good injection material.
【0021】さらに、該ポリマーセメント組成物の水/
セメント比は、強度発現性を考慮して20〜45%とす
ることが好ましく、該水/セメント比において注入剤と
しての流動性を確保するためには、流動化剤を添加する
ことが好ましい。流動化剤としては、リグニンスルホン
酸塩系、ナフタレンスルホン酸塩系、メラミンスルホン
酸塩系、ポリカルボン酸塩系の中から1種以上を選択し
て使用することができる。該流動化剤の混合割合は、前
記セメント100重量部に対して0.3〜3.0重量部
となるように添加することが好ましい。0.3重量部よ
り少なければ、注入時の作業性向上を十分に図ることが
できず、一方、3.0重量部より多く添加しても、それ
以上の効果を得ることができず逆にコスト高となる。Further, the polymer cement composition in water /
The cement ratio is preferably 20 to 45% in consideration of strength development, and it is preferable to add a fluidizing agent in order to secure fluidity as an injecting agent at the water / cement ratio. As the fluidizing agent, one or more selected from lignin sulfonate, naphthalene sulfonate, melamine sulfonate, and polycarboxylate can be used. The fluidizing agent is preferably added in an amount of 0.3 to 3.0 parts by weight with respect to 100 parts by weight of the cement. If it is less than 0.3 parts by weight, workability during injection cannot be sufficiently improved, while if it is added in excess of 3.0 parts by weight, no further effect can be obtained, and conversely. High cost.
【0022】尚、本発明のポリマーセメント組成物に
は、必要に応じて他の化学混和剤、即ち増粘剤、消泡
剤、金属アルミニウム系発泡剤などを添加しても良い。If desired, other chemical admixtures such as a thickener, a defoaming agent and a metallic aluminum-based foaming agent may be added to the polymer cement composition of the present invention.
【0023】本発明にかかるポリマーセメント組成物
は、従来知られている工法と同様の注入工法によって岩
塊のひび割れや岩塊の間隙に注入することができる。即
ち、まず初めに岩塊のひび割れや岩塊同士の間隙の周縁
部に注入口を残しつつ目地材を充填する。そして、前記
注入口より本発明にかかるポリマーセメント組成物を注
入し、ひび割れや間隙の全体を該注入材で充填し、固化
させる。The polymer cement composition according to the present invention can be injected into the cracks of rock masses or the spaces between rock masses by the injection method similar to the conventionally known method. That is, first, the joint material is filled while leaving the injection port in the peripheral portion of the crack of the rock mass and the gap between the rock masses. Then, the polymer cement composition according to the present invention is injected from the injection port, and cracks and gaps are entirely filled with the injection material and solidified.
【0024】ここでいう目地材としては、前記ポリマー
セメント組成物の配合を調整することにより、具体的に
はポリマーディスパージョンおよび混練水の量を減らし
て混練することにより、ポリマーセメント組成物より高
粘度のスラリー状に調製した目地材を好適に使用するこ
とができる。The joint material used herein is higher than the polymer cement composition by adjusting the composition of the polymer cement composition, specifically, by kneading the polymer dispersion and the kneading water in a reduced amount. A joint material prepared into a slurry having a viscosity can be preferably used.
【0025】このようにして、岩塊のひび割れや間隙
は、前記ポリマーセメント組成物によって略完全に充填
されることとなり、該注入材が固化することによって岩
塊全体が一体化されたものとなる。また、本発明にかか
るポリマーセメント組成物は、上述したように、セメン
トの乾燥収縮だけでなく、ポリマーディスパージョンに
起因する皮ばりやプラスチックひび割れをも効果的に抑
制されたものである。従って、充填された注入材(硬化
体)と岩塊との強固な接着状態が長期にわたって保たれ
ることとなり、岩塊の崩落防止効果がより永続的に維持
されることとなる。In this way, the cracks and gaps of the rock mass are almost completely filled with the polymer cement composition, and the entire rock mass is integrated by solidifying the injection material. . In addition, as described above, the polymer cement composition according to the present invention effectively suppresses not only the drying shrinkage of the cement but also the burrs and plastic cracks caused by the polymer dispersion. Therefore, a strong adhesive state between the filled injection material (hardened body) and the rock mass is maintained for a long period of time, and the effect of preventing the rock mass from collapsing is more permanently maintained.
【0026】[0026]
【実施例】下記に示すセメント材料を使用し、表1に示
す配合で実施例1〜3および比較例1〜3のポリマーセ
メント組成物を調製した。
(材料)
セメント:普通ポルトランドセメント、住友大阪セメン
ト(株)製
流動化剤:メラニン系流動化剤、日本シーカ(株)製、
シーカメントFF86/100
収縮低減剤:日本油脂(株)製、シュドックスE−40
繊維材料:ビニロン繊維、クラレ(株)製、RF−S6
02(6mm)
骨材:珪砂N40および珪砂N60(重量比3:2)EXAMPLES Using the cement materials shown below, the polymer cement compositions of Examples 1 to 3 and Comparative Examples 1 to 3 were prepared with the formulations shown in Table 1. (Material) Cement: Ordinary Portland cement, Sumitomo Osaka Cement Co., Ltd. Superplasticizer: Melanin-based superplasticizer, made by Nippon Sika Co., Ltd.,
Sikament FF86 / 100 Shrinkage reducing agent: NOF Corporation, Sudox E-40 Fiber material: Vinylon fiber, Kuraray Co., Ltd., RF-S6
02 (6 mm) Aggregate: Quartz sand N40 and Quartz sand N60 (weight ratio 3: 2)
【0027】[0027]
【表1】 [Table 1]
【0028】(試験1)コンクリート板を用いて型枠
(内寸:間口90cm×奥行30cm×厚み10cm)
を作成し、これを模擬的に岩塊のひび割れと仮定して前
記実施例および比較例のポリマーセメント組成物を充填
し、5、20、35℃にて促進試験を行った。結果を表
2に示す。(Test 1) Formwork using a concrete plate (inside dimension: frontage 90 cm x depth 30 cm x thickness 10 cm)
Was prepared, and the polymer cement compositions of the above Examples and Comparative Examples were filled on the assumption that the cracks of rock mass were simulated, and accelerated tests were carried out at 5, 20 and 35 ° C. The results are shown in Table 2.
【0029】[0029]
【表2】 [Table 2]
【0030】表2に示したように、PAE系およびSB
R系のポリマーディスバージョンを添加した実施例1お
よび2では、いずれの温度においてもひび割れが発生せ
ず、一方、同じくPAE系およびSBR系のポリマーデ
ィスバージョンを添加した比較例1および2では、収縮
低減材を添加しないために、いずれの温度においてもひ
び割れが発生した。As shown in Table 2, PAE system and SB
In Examples 1 and 2 in which the R-type polymer dispersion was added, cracks did not occur at any temperature, while in Comparative Examples 1 and 2 in which the PAE- and SBR-type polymer dispersions were added, shrinkage was observed. Since no reducing agent was added, cracking occurred at any temperature.
【0031】(試験2)前記実施例および比較例のポリ
マーセメント組成物について、JIS R 5201
「セメントの物理試験方法」に準じて凝結試験と、曲げ
および圧縮強度試験を行った。結果を表3に示す。(Test 2) Regarding the polymer cement compositions of the above Examples and Comparative Examples, JIS R 5201 was used.
A setting test and bending and compressive strength tests were performed according to the "physical test method for cement". The results are shown in Table 3.
【0032】[0032]
【表3】 [Table 3]
【0033】表3に示すように、EVA系のポリマーデ
ィスパージョンを用いた比較例1は、他のポリマーディ
スパージョンと比較して凝結時間が2倍以上かかること
が明らかである。また、圧縮強度および曲げ強度の試験
からも、EVA系のポリマーディスパージョンを用いた
比較例1が、強度発現性に劣ることが明らかである。As shown in Table 3, it is clear that the comparative example 1 using the EVA type polymer dispersion takes twice or more the setting time as compared with the other polymer dispersions. Also, from the tests of compressive strength and bending strength, it is clear that Comparative Example 1 using EVA-based polymer dispersion is inferior in strength development.
【0034】(試験3)PAE系のポリマーディスパー
ジョンを用いた実施例1および比較例2のポリマーセメ
ント組成物を使用し、JIS A 1171「ポリマー
セメントモルタルの試験方法」に準じて試験体を作製
し、JIS A 1129「モルタル及びコンクリート
の長さ変化試験方法」に準じて、打設の翌日を基長とし
て乾燥収縮を測定した。結果を表4に示す。(Test 3) Using the polymer cement compositions of Example 1 and Comparative Example 2 in which a PAE-based polymer dispersion was used, test samples were prepared according to JIS A 1171 "Testing method for polymer cement mortar". Then, in accordance with JIS A 1129 "Method for testing length change of mortar and concrete", dry shrinkage was measured with the next day of casting as the base length. The results are shown in Table 4.
【0035】[0035]
【表4】 [Table 4]
【0036】表4に示すように、収縮低減材を添加した
実施例1のポリマーセメント組成物によれば、8〜13
週におけるセメントの乾燥収縮が比較例の約1/2に低
減されており、なお且つ、硬化の初期(1日〜3日)の
収縮についても効果的に低減されていることがわかる。As shown in Table 4, according to the polymer cement composition of Example 1 containing the shrinkage-reducing material, 8 to 13
It can be seen that the dry shrinkage of cement during the week is reduced to about 1/2 of that of the comparative example, and the shrinkage at the initial stage of hardening (1 to 3 days) is also effectively reduced.
【0037】[0037]
【発明の効果】以上のように、本発明に係るポリマーセ
メント組成物によれば、プラスチックひび割れと乾燥収
縮の双方を効果的に抑制することができ、施工直後およ
び施工後数ヶ月経過した後にも施行面にひび割れの発生
を生じさせることがなく、安定した接着層を形成するこ
とができる。As described above, according to the polymer cement composition of the present invention, both plastic cracking and drying shrinkage can be effectively suppressed, and even immediately after the construction and after several months have passed. It is possible to form a stable adhesive layer without causing cracks on the applied surface.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) //(C04B 28/02 C04B 24:26 C 24:26 F G 16:06 Z 16:06) 111:70 111:70 (72)発明者 山本 高広 大阪市大正区南恩加島7丁目1番55号 住 友大阪セメント株式会社セメント・コンク リート研究所内 (72)発明者 久 修 茨城県つくば市桜1―17 ショーボンド建 設株式会社補修工学研究所内 (72)発明者 道脇 健一 茨城県つくば市桜1―17 ショーボンド建 設株式会社補修工学研究所内 Fターム(参考) 2D040 AA06 AB01 AB05 AB16 AC01 CA01 CA03 CA04 CA05 CA10 CB03 4G012 PA04 PA23 PA24 ─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. 7 Identification code FI theme code (reference) // (C04B 28/02 C04B 24:26 C 24:26 FG 16:06 Z 16:06) 111: 70 111: 70 (72) Inventor Takahiro Yamamoto 7-55, Minami Enkajima, Taisho-ku, Osaka City Sumitomo Osaka Cement Co., Ltd. Cement Concrete Research Institute (72) Inventor Hisamu 1 Sakura, Tsukuba City, Ibaraki Prefecture 17 Showbond Construction Co., Ltd. In the Repair Engineering Research Institute (72) Inventor Kenichi Dowaki 1-17 Sakura, Tsukuba City, Ibaraki Prefecture F-17 Term at the Showbond Construction Co., Ltd. Repair Engineering Research Laboratory (reference) 2D040 AA06 AB01 AB05 AB16 AC01 CA01 CA03 CA04 CA05 CA10 CB03 4G012 PA04 PA23 PA24
Claims (3)
脂系、スチレンブタジエン合成ゴム系、又は酢酸ビニル
ベオバアクリル共重合系のうち少なくとも1種のポリマ
ーと、界面活性作用を有する有機系の収縮低減剤とを含
有してなることを特徴とするポリマーセメント組成物。1. A shrinkage-reducing agent of cement, and at least one polymer selected from a polyacrylic acid ester resin system, a styrene-butadiene synthetic rubber system, or a vinyl acetate vinyl acrylate copolymer system, and an organic system having a surface-active action. A polymer cement composition comprising:
特徴とする請求項1記載のポリマーセメント組成物。2. The polymer cement composition according to claim 1, further comprising a fiber material.
徴とする請求項1又は2記載のポリマーセメント組成
物。3. The polymer cement composition according to claim 1, further comprising an expansive material.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001246750A JP3638894B2 (en) | 2001-08-15 | 2001-08-15 | Polymer cement composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001246750A JP3638894B2 (en) | 2001-08-15 | 2001-08-15 | Polymer cement composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2003055018A true JP2003055018A (en) | 2003-02-26 |
JP3638894B2 JP3638894B2 (en) | 2005-04-13 |
Family
ID=19076230
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2001246750A Expired - Fee Related JP3638894B2 (en) | 2001-08-15 | 2001-08-15 | Polymer cement composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3638894B2 (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005082416A (en) * | 2003-09-05 | 2005-03-31 | Denki Kagaku Kogyo Kk | Polymer cement composition, polymer cement grout mortar, and repair material using the same |
JP2005281036A (en) * | 2004-03-29 | 2005-10-13 | Sumitomo Osaka Cement Co Ltd | Polymer cement-based mortar for use in tile joint and manufacturing method therefor |
JP2007269508A (en) * | 2006-03-30 | 2007-10-18 | Ube Ind Ltd | Hydraulic composition |
JP2008037704A (en) * | 2006-08-07 | 2008-02-21 | Sho Bond Constr Co Ltd | Method for repairing concrete channel |
JP2008120612A (en) * | 2006-11-09 | 2008-05-29 | Denki Kagaku Kogyo Kk | Grout composition, grout mortar and grout method |
JP2008120611A (en) * | 2006-11-09 | 2008-05-29 | Denki Kagaku Kogyo Kk | Grout composition, grout mortar and grout method |
KR101280072B1 (en) * | 2010-12-28 | 2013-07-08 | (주)콘스텍 | Injection type rapidly hardening method to pave road using recycled aggregates |
JP2020122327A (en) * | 2019-01-30 | 2020-08-13 | 株式会社Core技術研究所 | Composite pile, and construction method of composite pile |
-
2001
- 2001-08-15 JP JP2001246750A patent/JP3638894B2/en not_active Expired - Fee Related
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005082416A (en) * | 2003-09-05 | 2005-03-31 | Denki Kagaku Kogyo Kk | Polymer cement composition, polymer cement grout mortar, and repair material using the same |
JP4493957B2 (en) * | 2003-09-05 | 2010-06-30 | 電気化学工業株式会社 | Polymer cement composition, polymer cement grout mortar, and repair material using the same |
JP2005281036A (en) * | 2004-03-29 | 2005-10-13 | Sumitomo Osaka Cement Co Ltd | Polymer cement-based mortar for use in tile joint and manufacturing method therefor |
JP2007269508A (en) * | 2006-03-30 | 2007-10-18 | Ube Ind Ltd | Hydraulic composition |
JP2008037704A (en) * | 2006-08-07 | 2008-02-21 | Sho Bond Constr Co Ltd | Method for repairing concrete channel |
JP2008120612A (en) * | 2006-11-09 | 2008-05-29 | Denki Kagaku Kogyo Kk | Grout composition, grout mortar and grout method |
JP2008120611A (en) * | 2006-11-09 | 2008-05-29 | Denki Kagaku Kogyo Kk | Grout composition, grout mortar and grout method |
KR101280072B1 (en) * | 2010-12-28 | 2013-07-08 | (주)콘스텍 | Injection type rapidly hardening method to pave road using recycled aggregates |
JP2020122327A (en) * | 2019-01-30 | 2020-08-13 | 株式会社Core技術研究所 | Composite pile, and construction method of composite pile |
JP7201968B2 (en) | 2019-01-30 | 2023-01-11 | 株式会社Core技術研究所 | Composite pile and construction method of composite pile |
Also Published As
Publication number | Publication date |
---|---|
JP3638894B2 (en) | 2005-04-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2625836C (en) | Slump retention in cementitious compositions | |
CN104973832B (en) | Anti-crack mortar and preparation method therefor | |
EP3307690A1 (en) | Advanced fiber reinforced concrete mix designs | |
JP2008120611A (en) | Grout composition, grout mortar and grout method | |
JP2009132557A (en) | Admixture for polymer cement grout | |
JP2003055018A (en) | Polymer cement composition | |
CN115557767A (en) | Lime-based mortar, and preparation method and application thereof | |
JPH01261250A (en) | Admixture for cement concrete and mortar produced by using highly water-absorbing resin | |
JP4125009B2 (en) | Cement-based PC grout composition | |
JP6985177B2 (en) | Hydraulic composition and concrete | |
JP5378754B2 (en) | Polymer cement composition | |
CN108264270B (en) | Environment-friendly slurry for paving metal floor tiles | |
JP2627936B2 (en) | Inorganic elastic injection material | |
JPH0517196A (en) | Grouting material for repairing concrete structure | |
JP2004189512A (en) | Composition of mortar | |
JP4108165B2 (en) | Resin mortar composition | |
JP5270258B2 (en) | CEMENT-BASED GROUT COMPOSITION AND METHOD FOR PRODUCING PREGROUT PC STEEL USING THE COMPOSITION | |
JPH1171157A (en) | Hydraulic composition | |
JPH0637319B2 (en) | Method for curing cement composition | |
JPS62256752A (en) | Self levelling mortar | |
JPS6360175A (en) | Lightweight mortar | |
JP2006273597A (en) | Polymer cement mortar for tile adhesion | |
CN119263756A (en) | Ultra-fine grouting material for repairing narrow cracks in concrete in high-cold environments, preparation method and application thereof | |
JP2964036B1 (en) | Finishing cement-based composition and method for producing cement-based molded article using the same | |
JP2003321264A (en) | Hydraulic composition and its hardened body |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20031226 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20040224 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20040528 |
|
RD04 | Notification of resignation of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7424 Effective date: 20040706 |
|
RD04 | Notification of resignation of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7424 Effective date: 20040707 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20050107 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20050112 |
|
R150 | Certificate of patent or registration of utility model |
Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20080121 Year of fee payment: 3 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20090121 Year of fee payment: 4 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20090121 Year of fee payment: 4 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20100121 Year of fee payment: 5 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110121 Year of fee payment: 6 |
|
LAPS | Cancellation because of no payment of annual fees |