JP5785429B2 - Cement admixture and cement composition - Google Patents
Cement admixture and cement composition Download PDFInfo
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- JP5785429B2 JP5785429B2 JP2011096726A JP2011096726A JP5785429B2 JP 5785429 B2 JP5785429 B2 JP 5785429B2 JP 2011096726 A JP2011096726 A JP 2011096726A JP 2011096726 A JP2011096726 A JP 2011096726A JP 5785429 B2 JP5785429 B2 JP 5785429B2
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- 239000004568 cement Substances 0.000 title claims description 39
- 239000000203 mixture Substances 0.000 title claims description 12
- 239000000463 material Substances 0.000 claims description 33
- 239000003638 chemical reducing agent Substances 0.000 claims description 24
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 125000002947 alkylene group Chemical group 0.000 claims description 8
- 239000004571 lime Substances 0.000 claims description 8
- -1 polyoxypropylene Polymers 0.000 claims description 8
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims description 7
- 235000011941 Tilia x europaea Nutrition 0.000 claims description 7
- 150000001346 alkyl aryl ethers Chemical class 0.000 claims description 7
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims description 7
- 229920001577 copolymer Polymers 0.000 claims description 7
- 229920001451 polypropylene glycol Polymers 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- 239000002994 raw material Substances 0.000 description 21
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 10
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 9
- 229910004298 SiO 2 Inorganic materials 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 6
- 239000004567 concrete Substances 0.000 description 6
- 229910052500 inorganic mineral Inorganic materials 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000011707 mineral Substances 0.000 description 6
- 235000010755 mineral Nutrition 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- 239000010440 gypsum Substances 0.000 description 4
- 229910052602 gypsum Inorganic materials 0.000 description 4
- 239000004570 mortar (masonry) Substances 0.000 description 4
- 239000004576 sand Substances 0.000 description 4
- 235000019738 Limestone Nutrition 0.000 description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
- 239000000378 calcium silicate Substances 0.000 description 3
- 229910052918 calcium silicate Inorganic materials 0.000 description 3
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 3
- 239000006028 limestone Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000011398 Portland cement Substances 0.000 description 2
- 229910001570 bauxite Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 235000011116 calcium hydroxide Nutrition 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- 150000004683 dihydrates Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000000634 powder X-ray diffraction Methods 0.000 description 2
- 238000007873 sieving Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 229910018068 Li 2 O Inorganic materials 0.000 description 1
- 238000003991 Rietveld refinement Methods 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 229910010413 TiO 2 Inorganic materials 0.000 description 1
- 229920002978 Vinylon Polymers 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 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
- 238000004458 analytical method Methods 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000007798 antifreeze agent Substances 0.000 description 1
- 239000002956 ash Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- ZOMBKNNSYQHRCA-UHFFFAOYSA-J calcium sulfate hemihydrate Chemical compound O.[Ca+2].[Ca+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O ZOMBKNNSYQHRCA-UHFFFAOYSA-J 0.000 description 1
- WETINTNJFLGREW-UHFFFAOYSA-N calcium;iron;tetrahydrate Chemical compound O.O.O.O.[Ca].[Fe].[Fe] WETINTNJFLGREW-UHFFFAOYSA-N 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000011083 cement mortar Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000002734 clay mineral Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000010334 sieve classification Methods 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Landscapes
- Curing Cements, Concrete, And Artificial Stone (AREA)
Description
本発明は、土木・建築分野において使用されるコンクリート用膨張材およびその製造方法に関する。 The present invention relates to a concrete expansion material used in the field of civil engineering and construction, and a method for producing the same.
少ない添加量で優れた膨張特性を有するコンクリート膨張材が提案されている(特許文献1参照)。また、これら膨張材に収縮低減剤を添加し、膨張材と収縮低減剤を組み合わせて膨張性能と収縮低減性能を両立したセメント混和材が提案されている(特許文献2、3参照)。
さらに、膨張材の粒度を調整することによって、ポップアウトを防止し、膨張率を確保する技術が開示されている(特許文献4、5参照)。しかしながら、これら文献では、200〜300μm、90μm、あるいは、5〜20μm、150μmなどにおける粒度調整であった。
A concrete expansion material having excellent expansion characteristics with a small addition amount has been proposed (see Patent Document 1). In addition, cement admixtures that have both expansion performance and shrinkage reduction performance by adding a shrinkage reduction agent to these expansion materials and combining the expansion material and the shrinkage reduction agent have been proposed (see Patent Documents 2 and 3).
Furthermore, a technique for preventing pop-out and ensuring an expansion rate by adjusting the particle size of the expansion material is disclosed (see Patent Documents 4 and 5). However, in these documents, particle size adjustment was performed at 200 to 300 μm, 90 μm, 5 to 20 μm, 150 μm, and the like.
本発明は、特定の膨張材を特定の粒度で調整することにより、従来よりもさらにポップアウトを防止でき、膨張ひずみを大きくすることが可能であることを知見したものである。
また、膨張材を収縮低減剤でスラリー化した材料は性能面で優れるものの、収縮低減剤はコストが高いため、できるだけ収縮低減剤の配合割合を抑えた材料が求められていた。しかしながら、収縮低減剤の添加量を抑えると膨張材が凝集してポップアウト現象が起きたり、膨張ひずみの増加効果が小さくなるなどの課題があった。
本発明は、特定の膨張材を使用することで、収縮低減剤を配合しないか従来よりも収縮低減剤の添加量を抑えても、上記課題を解決することを知見したものである。
The present invention has been found that by adjusting a specific expansion material with a specific particle size, pop-out can be further prevented and expansion strain can be increased.
In addition, although a material obtained by slurrying an expansion material with a shrinkage reducing agent is excellent in terms of performance, the shrinkage reducing agent has a high cost. Therefore, a material in which the blending ratio of the shrinkage reducing agent is suppressed as much as possible has been demanded. However, when the amount of the shrinkage reducing agent added is suppressed, there are problems such that the expansion material aggregates to cause a pop-out phenomenon, and the effect of increasing the expansion strain is reduced.
The present invention has been found that the use of a specific expansion material solves the above-described problem even if a shrinkage reducing agent is not blended or the amount of shrinkage reducing agent added is suppressed as compared with the prior art.
すなわち、本発明は、(1)遊離石灰、水硬性化合物、無水石膏を含有してなり、45μm篩残分が40質量%以上で90μm篩残分が30質量%以下である膨張材と収縮低減剤を含有してなり、収縮低減剤がアルキレンオキサイド・プロピレンオキサイド共重合体とポリオキシプロピレンモノアルキルエーテルを併用したものであるセメント混和材、(2)膨張材が80〜95質量部、収縮低減剤が5〜20質量部である(1)のセメント混和材、(3)セメントと(1)または(2)のセメント混和材とを含有してなるセメント組成物、である。 That is, the present invention includes (1) an expanded material containing free lime, a hydraulic compound, and anhydrous gypsum, a 45 μm sieve residue of 40% by mass or more and a 90 μm sieve residue of 30% by mass or less and shrinkage reduction. agent and also contains, cement admixture shrinkage reducing agent is obtained by a combination of alkylene oxide-propylene oxide copolymer and polyoxypropylene monoalkyl ether, (2) Rise stretched member is 80 to 95 parts by mass, shrinkage ( 1 ) a cement admixture containing 5 to 20 parts by mass of a reducing agent , (3 ) a cement composition containing cement and (1) or (2) a cement admixture.
本発明のセメント混和材は、収縮低減剤を配合しないか従来よりも収縮低減剤の配合割合を抑えても膨張材の凝集を抑制でき、ポップアウトが無く、従来と同等以上の膨張ひずみを満足するセメント混和材を提供する。 The cement admixture of the present invention can suppress the aggregation of the expansion material even if the shrinkage reducing agent is not blended or the blending ratio of the shrinkage reducing agent is less than that of the conventional one, has no pop-out, and satisfies the same or larger expansion strain than the conventional one. A cement admixture is provided.
なお、本発明で使用する部、%は、特に規定しない限り質量基準である。
また、本発明で云うコンクリートとは、セメントペースト、セメントモルタル、セメントコンクリートを総称するものである。
The parts and% used in the present invention are based on mass unless otherwise specified.
The concrete referred to in the present invention is a generic term for cement paste, cement mortar, and cement concrete.
本発明で使用する膨張材は、CaO原料、Al2O3原料、Fe2O3原料、SiO2原料、およびCaSO4原料を適宜混合して熱処理して得られる遊離石灰、水硬性化合物、無水石膏を含有するクリンカを所定の粒度に粉砕して得られるものである。
本発明で云う遊離石灰とは、通常f−CaOと呼ばれるものである。
本発明で云う水硬性化合物とは、3CaO・3Al2O3・CaSO4で表されるアウイン、3CaO・SiO2(C3Sと略記)や2CaO・SiO2(C2Sと略記)で表されるカルシウムシリケート、4CaO・Al2O3・Fe2O3(C4AFと略記)や6CaO・2Al2O3・Fe2O3(C6A2Fと略記)、6CaO・Al2O3・Fe2O3(C6AFと略記)で表されるカルシウムアルミノフェライト、2CaO・Fe2O3(C2Fと略記)等のカルシウムフェライトなどであり、これらのうちの1種または2種以上を含むことが好ましい。
本発明で云う無水石膏とは、CaSO4と表記されるものである。
The expansion material used in the present invention is a free lime, hydraulic compound, anhydrous obtained by heat-mixing CaO raw material, Al 2 O 3 raw material, Fe 2 O 3 raw material, SiO 2 raw material, and CaSO 4 raw material as appropriate. It is obtained by pulverizing a clinker containing gypsum to a predetermined particle size.
The free lime referred to in the present invention is usually called f-CaO.
Table In the hydraulic compound referred to in the present invention, Auin represented by 3CaO · 3Al 2 O 3 · CaSO 4, 3CaO · SiO 2 (C 3 S for short) and 2CaO · SiO 2 (C 2 S for short) Calcium silicate, 4CaO.Al 2 O 3 .Fe 2 O 3 (abbreviated as C 4 AF), 6CaO.2Al 2 O 3 .Fe 2 O 3 (abbreviated as C 6 A 2 F), 6CaO.Al 2 O Calcium aluminoferrite represented by 3 · Fe 2 O 3 (abbreviated as C 6 AF), calcium ferrite such as 2CaO · Fe 2 O 3 (abbreviated as C 2 F), and one or two of these Preferably it contains more than one species.
The anhydrous gypsum referred to in the present invention is expressed as CaSO 4 .
CaO原料としては石灰石や消石灰が挙げられ、Al2O3原料としてはボーキサイトやアルミ残灰などが挙げられ、Fe2O3原料としては銅カラミや市販の酸化鉄が、SiO2原料としては珪石等が、CaSO4原料としては二水石膏、半水石膏および無水石膏が挙げられる。これら原料には不純物を含む場合があるが、本発明の効果を阻害しない範囲内では特に問題とはならない。不純物としては、MgO、TiO2、ZrO2、MnO、P2O5、Na2O、K2O、Li2O、硫黄、フッ素、塩素などが挙げられる。 Examples of the CaO raw material include limestone and slaked lime, examples of the Al 2 O 3 raw material include bauxite and aluminum residual ash, examples of the Fe 2 O 3 raw material include copper calami and commercially available iron oxide, and examples of the SiO 2 raw material include silica stone. However, examples of the CaSO 4 raw material include dihydrate gypsum, hemihydrate gypsum, and anhydrous gypsum. These raw materials may contain impurities, but this is not a problem as long as the effects of the present invention are not impaired. Examples of impurities include MgO, TiO 2 , ZrO 2 , MnO, P 2 O 5 , Na 2 O, K 2 O, Li 2 O, sulfur, fluorine, and chlorine.
本発明で使用する膨張材に使用するクリンカの熱処理方法は特に限定されるものではないが、電気炉やキルンなどを用いて1100〜1600℃の温度で焼成することが好ましく、1200〜1500℃がより好ましい。1100℃未満では膨張性能が充分でなく、1600℃を超えると無水石膏が分解する場合がある。 Although the heat processing method of the clinker used for the expansion material used by this invention is not specifically limited, It is preferable to bake at the temperature of 1100-1600 degreeC using an electric furnace, a kiln, etc., and 1200-1500 degreeC is. More preferred. If it is less than 1100 ° C., the expansion performance is not sufficient, and if it exceeds 1600 ° C., anhydrous gypsum may decompose.
本発明で使用する膨張材に使用するクリンカに含まれる各鉱物の割合は、以下の範囲であることが好ましい。遊離石灰の含有量は、クリンカ100部中、30〜70部が好ましく、40〜60部がより好ましい。水硬性化合物の含有量は、クリンカ100部中、10〜40部が好ましく、20〜30部がより好ましい。無水石膏の含有量は、クリンカ100部中、10〜40部が好ましく20〜30部がより好ましい。前記範囲外では、膨張量が小さくなったり、逆に極端に大きくなって圧縮強度が低下したりする場合がある。 It is preferable that the ratio of each mineral contained in the clinker used for the expansion material used by this invention is the following ranges. The content of free lime is preferably 30 to 70 parts, more preferably 40 to 60 parts, in 100 parts of clinker. As for content of a hydraulic compound, 10-40 parts are preferable in 100 parts of clinker, and 20-30 parts are more preferable. The content of anhydrous gypsum is preferably 10 to 40 parts and more preferably 20 to 30 parts in 100 parts of clinker. Outside the above range, the amount of expansion may decrease, or conversely, it may become extremely large and the compression strength may decrease.
鉱物の含有量は、従来一般の分析方法で確認することができる。例えば、粉砕した試料を粉末X線回折装置にかけ、生成鉱物を確認するとともにデータをリートベルト法にて解析し、鉱物を定量することができる。また、化学成分と粉末X線回折の同定結果に基づいて、鉱物量を計算によって求めることもできる。 The mineral content can be confirmed by a conventional analysis method. For example, the pulverized sample can be applied to a powder X-ray diffractometer to confirm the produced mineral and analyze the data by the Rietveld method to quantify the mineral. Further, based on the identification result of chemical components and powder X-ray diffraction, the amount of minerals can also be obtained by calculation.
本発明で使用する膨張材の粉末度は特に重要であり、45μm篩残分が40%以上かつ90μm篩残分が30%以下であることが好ましく、45μm篩残分が80%以上かつ90μm篩残分が20%未満であることがより好ましい。前記範囲では膨張量が小さくなったり、ポップアウトが生じ易くなったりする場合がある。
粉末度の調整方法は特に限定されるものではなく、気流分級法、ふるい分級方式などが適用可能である。
The fineness of the expandable material used in the present invention is particularly important. The 45 μm sieve residue is preferably 40% or more and the 90 μm sieve residue is preferably 30% or less, and the 45 μm sieve residue is 80% or more and 90 μm sieve. More preferably, the balance is less than 20%. In the above range, the amount of expansion may be small, or pop-out may easily occur.
The method for adjusting the fineness is not particularly limited, and an airflow classification method, a sieve classification method, and the like are applicable.
本発明で使用する収縮低減剤の種類は、特に限定されるものではなく、アルキレンオキサイド・プロピレンオキサイド共重合体、ポリオキシプロピレンモノアルキルエーテル、グリコールエーテル・アミノアルコール誘導体、低級アルコールのアルキレンオキシド付加物などが使用可能で、特に、アルキレンオキサイド・プロピレンオキサイド共重合体とポリオキシプロピレンモノアルキルエーテルを併用することが、膨張性能の観点から好ましい。 The kind of shrinkage reducing agent used in the present invention is not particularly limited, and alkylene oxide / propylene oxide copolymer, polyoxypropylene monoalkyl ether, glycol ether / amino alcohol derivative, and alkylene oxide adduct of lower alcohol. In particular, the combined use of an alkylene oxide / propylene oxide copolymer and a polyoxypropylene monoalkyl ether is preferable from the viewpoint of expansion performance.
本発明で膨張材に収縮低減剤を併用する場合、膨張材と収縮低減剤の合計100部中、収縮低減剤の割合は20部以下であり、3〜20部が好ましく、5〜15部がより好ましい。20部を越えると膨張ひずみが小さくなる場合がある。 In the present invention, when a shrinkage reducing agent is used in combination with the expansion material, the ratio of the shrinkage reduction agent is 20 parts or less, preferably 3 to 20 parts, and preferably 5 to 15 parts in a total of 100 parts of the expansion material and the shrinkage reduction agent. More preferred. If it exceeds 20 parts, the expansion strain may be reduced.
本発明のセメント混和材の使用量は、コンクリートの配合によって変化するため特に限定されるものではないが、通常、セメントとセメント混和材からなるセメント組成物100部中、3〜10部が好ましく、5〜8部がより好ましい。3部未満では充分な膨張性能が得られない場合があり、10部を超えて使用すると過膨張となりコンクリートに膨張クラックを生じる場合がある。 The amount of the cement admixture of the present invention is not particularly limited because it varies depending on the blending of concrete, but usually 3 to 10 parts are preferable in 100 parts of a cement composition composed of cement and a cement admixture, 5-8 parts is more preferable. If it is less than 3 parts, sufficient expansion performance may not be obtained, and if it exceeds 10 parts, it may overexpand and may cause expansion cracks in the concrete.
本発明のセメント組成物で使用するセメントとしては、普通、早強、超早強、低熱、および中庸熱などの各種ポルトランドセメント、これらセメントに高炉スラグ、フライアッシュ、シリカを混合した各種混合セメント、ならびに石灰石粉末を混合したフィラーセメントなどが挙げられる。 As the cement used in the cement composition of the present invention, various portland cements such as normal, early strength, super early strength, low heat, and moderate heat, various mixed cements obtained by mixing blast furnace slag, fly ash and silica with these cements, And filler cement mixed with limestone powder.
本発明では、砂、砂利、減水剤、高性能減水剤、AE減水剤、高性能AE減水剤、流動化剤、消泡剤、増粘剤、防錆剤、防凍剤、高分子エマルジョン、および凝結調整剤、ならびにセメント急硬材、ベントナイト等の粘土鉱物、ゼオライトなどのイオン交換体、シリカ質微粉末、炭酸カルシウム、水酸化カルシウム、石膏、ケイ酸カルシウムなどが挙げられ、有機系材料としては、ビニロン繊維、アクリル繊維、炭素繊維などの繊維状物質が挙げられる。 In the present invention, sand, gravel, water reducing agent, high performance water reducing agent, AE water reducing agent, high performance AE water reducing agent, fluidizing agent, antifoaming agent, thickener, rust preventive agent, antifreeze agent, polymer emulsion, and Examples of setting modifiers include cement hardeners, clay minerals such as bentonite, ion exchangers such as zeolite, siliceous fine powder, calcium carbonate, calcium hydroxide, gypsum, calcium silicate, etc. And fibrous materials such as vinylon fiber, acrylic fiber, and carbon fiber.
以下、実施例で詳細に説明する。 Examples will be described in detail below.
「実験例1」
遊離石灰50部、アウイン10部、カルシウムアルミノフェライト(4CaO・Al2O3・Fe2O3)5部、カルシウムシリケート(2CaO・SiO2)5部、無水石膏30部となるように、CaO原料、Al2O3原料、Fe2O3原料、SiO2原料、CaSO4原料を調合し、1350℃で熱処理して膨張材クリンカを合成した。この膨張材クリンカをボールミルを用いて粉砕し、ふるいを用いて表1に示すような粒度に調製した。ふるいはJIS Z 8801−1に規定されている金属製網ふるいの目開きが300μm、90μm、45μmのものを用いた。
表1に示すように、膨張材からなるセメント混和材と、膨張材85部と収縮低減剤15部からなるセメント混和材を調製した。
セメントとセメント混和材からなるセメント組成物100部中、セメント混和材を7部使用し、水/セメント組成物比=50%、セメント組成物/砂比=1/3のモルタルを20℃の室内で調製して、長さ変化率(膨張ひずみ)の測定を行った。また、ポップアウト試験を行った。なお、市販の膨張材についても同様の評価を行った。結果を表1に示す。
"Experiment 1"
CaO raw material so that it becomes 50 parts of free lime, 10 parts of Auin, 5 parts of calcium aluminoferrite (4CaO.Al 2 O 3 .Fe 2 O 3 ), 5 parts of calcium silicate (2CaO.SiO 2 ), and 30 parts of anhydrous gypsum. Then, Al 2 O 3 raw material, Fe 2 O 3 raw material, SiO 2 raw material, and CaSO 4 raw material were prepared and heat-treated at 1350 ° C. to synthesize an expansion material clinker. The intumescent clinker was pulverized using a ball mill and adjusted to a particle size as shown in Table 1 using a sieve. As the sieve, a metal mesh sieve having a mesh size of 300 μm, 90 μm, and 45 μm as defined in JIS Z8801-1 was used.
As shown in Table 1, a cement admixture composed of an expansion material and a cement admixture composed of 85 parts of the expansion material and 15 parts of the shrinkage reducing agent were prepared.
Among 100 parts of cement composition consisting of cement and cement admixture, 7 parts of cement admixture were used, water / cement composition ratio = 50%, cement composition / sand ratio = 1/3 mortar at 20 ° C. The length change rate (expansion strain) was measured. A pop-out test was also conducted. The same evaluation was performed on a commercially available expansion material. The results are shown in Table 1.
(使用材料)
CaO原料:石灰石
Al2O3原料:ボーキサイト
Fe2O3原料:酸化鉄
SiO2原料:珪石
CaSO4原料:二水石膏
砂:JIS標準砂
水:水道水
セメント:普通ポルトランドセメント、市販品
収縮低減剤A:アルキレンオキサイドとプロピレンオキサイドの共重合体50部と、ポリオキシプロピレンモノアルキルエーテル50部の混合物
収縮低減剤B:アルキレンオキサイドとプロピレンオキサイドの共重合体
ここで、アルキレンオキサイドとプロピレンオキサイドの共重合体の平均的な構造式は、HO−(C3H6O11.3/C2H4O3.7)−Hで表せる。また、ポリオキシプロピレンモノアルキルエーテルの平均的な構造式は、C4H9O−(C2H4O)2−(C3H6O)2−Hで表せる。
収縮低減剤C:ポリグリコールエーテル化合物
市販の膨張材(1):エトリンガイト−石灰複合系膨張材
市販の膨張材(2):石灰系膨張材
(Materials used)
CaO raw material: limestone Al 2 O 3 raw material: bauxite Fe 2 O 3 raw material: iron oxide SiO 2 raw material: silica CaSO 4 raw material: dihydrate gypsum sand: JIS standard sand water: tap water cement: ordinary Portland cement, reduction of shrinkage on commercial products Agent A: Mixture shrinkage reducing agent of 50 parts of a copolymer of alkylene oxide and propylene oxide and 50 parts of polyoxypropylene monoalkyl ether B: Copolymer of alkylene oxide and propylene oxide Here, a copolymer of alkylene oxide and propylene oxide The average structural formula of the polymer can be represented by HO— (C 3 H 6 O 11.3 / C 2 H 4 O 3.7 ) —H. The average structural formula of polyoxypropylene monoalkyl ether can be represented by C 4 H 9 O— (C 2 H 4 O) 2 — (C 3 H 6 O) 2 —H.
Shrinkage reducing agent C: Polyglycol ether compound commercially available expansion material (1): Ettlingite-lime composite expansion material Commercial expansion material (2): Lime-based expansion material
(試験方法)
鉱物組成:化学組成と粉末X線回折の同定結果に基づいて計算により求めた。
長さ変化率:JIS A 6202 付属書1 膨張材のモルタルによる膨張性試験方法に準じ材齢7日までの膨張ひずみを測定した。
ポップアウト試験:練り混ぜたモルタルを20×20×5cmの平板状に成型して表面を平滑にし、20℃60%室内で6ヶ月間養生した後、モルタル表面を観察してポップアウトの有無を確認した。
(Test method)
Mineral composition: Obtained by calculation based on the chemical composition and the identification result of powder X-ray diffraction.
Length change rate: JIS A 6202 Appendix 1 The expansion strain up to 7 days of age was measured according to the expansibility test method using mortar of expansive material.
Pop-out test: Kneaded mortar is molded into a flat plate of 20 x 20 x 5 cm to smooth the surface. After curing for 6 months in a room at 20 ° C and 60%, the surface of the mortar is observed for the presence or absence of pop-out. confirmed.
「実験例2」
膨張材の粒度を45μm篩い残分が100%、90μm篩い残分が30%に、収縮低減剤をAに固定し、膨張材と収縮低減剤の配合比率を表2に示すように変化させたこと以外は実験例1と同様に行った。結果を表2に示す。
"Experimental example 2"
The particle size of the expansion material was 45% sieving residue 100%, 90 μm sieving residue 30%, the shrinkage reducing agent was fixed to A, and the mixing ratio of the expansion material and the shrinkage reducing agent was changed as shown in Table 2. Except for this, the same procedure as in Experimental Example 1 was performed. The results are shown in Table 2.
「実験例3」
セメント混和材の添加量を表3に示すように変化させたこと以外は実験例2と同様に行った。結果を表3に示す。
"Experiment 3"
The procedure was the same as in Experimental Example 2 except that the amount of cement admixture added was changed as shown in Table 3. The results are shown in Table 3.
本発明のセメント混和材およびセメント組成物により、高価な収縮低減剤の配合割合を抑えても、ポップアウトの発生が無く、良好な膨張ひずみが得られるため、土木、建築分野で幅広く使用できる。 With the cement admixture and the cement composition of the present invention, even if the blending ratio of the expensive shrinkage reducing agent is suppressed, pop-out does not occur and good expansion strain can be obtained.
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