JP2008162835A - Efflorescence inhibition method for alkali metal salt - Google Patents
Efflorescence inhibition method for alkali metal salt Download PDFInfo
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- JP2008162835A JP2008162835A JP2006353381A JP2006353381A JP2008162835A JP 2008162835 A JP2008162835 A JP 2008162835A JP 2006353381 A JP2006353381 A JP 2006353381A JP 2006353381 A JP2006353381 A JP 2006353381A JP 2008162835 A JP2008162835 A JP 2008162835A
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- -1 alkali metal salt Chemical class 0.000 title claims abstract description 48
- 229910052783 alkali metal Inorganic materials 0.000 title claims abstract description 47
- 238000000034 method Methods 0.000 title claims abstract description 33
- 238000006253 efflorescence Methods 0.000 title abstract 4
- 206010037844 rash Diseases 0.000 title abstract 4
- 230000005764 inhibitory process Effects 0.000 title abstract 3
- 239000002245 particle Substances 0.000 claims abstract description 48
- 239000004568 cement Substances 0.000 claims abstract description 26
- 239000000843 powder Substances 0.000 claims abstract description 25
- 239000004570 mortar (masonry) Substances 0.000 claims abstract description 23
- 239000004567 concrete Substances 0.000 claims abstract description 16
- 239000006072 paste Substances 0.000 claims abstract description 16
- 239000000945 filler Substances 0.000 claims description 14
- 230000002265 prevention Effects 0.000 claims description 9
- 238000012856 packing Methods 0.000 abstract description 8
- 239000000203 mixture Substances 0.000 description 11
- 238000003860 storage Methods 0.000 description 10
- 229910021532 Calcite Inorganic materials 0.000 description 6
- 238000011161 development Methods 0.000 description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 229910052593 corundum Inorganic materials 0.000 description 4
- 239000010431 corundum Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000011398 Portland cement Substances 0.000 description 3
- 230000004075 alteration Effects 0.000 description 3
- 230000007774 longterm Effects 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 230000015271 coagulation Effects 0.000 description 2
- 238000005345 coagulation Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000006703 hydration reaction Methods 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- KWMLJOLKUYYJFJ-UHFFFAOYSA-N 2,3,4,5,6,7-Hexahydroxyheptanoic acid Chemical class OCC(O)C(O)C(O)C(O)C(O)C(O)=O KWMLJOLKUYYJFJ-UHFFFAOYSA-N 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical class OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910052936 alkali metal sulfate Inorganic materials 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 150000004645 aluminates Chemical class 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical class OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000010883 coal ash Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical compound [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229910021487 silica fume Inorganic materials 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 235000011006 sodium potassium tartrate Nutrition 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 238000012360 testing method 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
- 230000000007 visual effect Effects 0.000 description 1
Landscapes
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
Description
本発明は、セメントペースト、モルタル又はコンクリートに例えば凝結調整剤などとして使用されるアルカリ金属塩の風化を防止する方法に関する。 The present invention relates to a method for preventing weathering of alkali metal salts used as cement control agents, for example, in cement paste, mortar or concrete.
セメントペースト、モルタル又はコンクリート等のセメントを含有する水硬性組成物では、水和反応による凝結を調整すめために、アルカリ金属の硫酸塩、炭酸塩、硝酸塩（以上、凝結促進作用）、オキシカルボン酸塩（凝結遅延作用）等のアルカリ金属塩を配合使用することが知られている。（例えば、特許文献１〜２参照。）一方で、アルカリ金属塩は非常に吸湿性が高く、大気中の水分等を吸収すると潮解が起こる。潮解が進んだアルカリ金属塩は概して高アルカリ質の高粘性流体となるので取扱に特段の配慮が必要となる他、凝結調整作用が著しく低下し、セメントペースト、モルタル又はコンクリート等で所望の強度発現性が得られなくなる。このため、アルカリ金属塩の長期間の保存は容易でなく、密封性の高い容器に入れて脱気するか又は不活性ガスを充填する方法か、外部水分との接触を遮断することができる樹脂等でアルカリ金属塩の粒子表面を被覆する（例えば、特許文献３参照。）といった何れも非常に手間のかかる方法で対応されてきた。
本発明は、セメントペースト、モルタル又はコンクリート等に配合使用する潮解性の高いアルカリ金属塩を、手間のかかる処理や特別の設備・容器等を使用しなくとも、潮解等の風化を起こさせずに、その凝結調整能力を維持したまま長期間安定に保存させるための風化防止方法を提供する。 The present invention is a highly deliquescent alkali metal salt used in cement paste, mortar, concrete, or the like, without requiring time-consuming treatment or special equipment / vessels, etc. without causing weathering such as deliquescence. The present invention provides a weathering prevention method for stably storing for a long period of time while maintaining its setting ability.
本発明者は、課題解決のため鋭意検討を重ねた結果、アルカリ金属塩と共にセメントペースト、モルタル又はコンクリート等に配合使用される材料のうち、非潮解質の無機粉末の中から何れか１種又は２種以上を選定し、この選定した無機粉末の粒度を微粒にし、これにアルカリ金属塩を分散させたものを充填体にすることにより、当該無機粉末の保存に準じた通常の保存方法で、例えば１００日以上の長期間保存しても、アルカリ金属塩の潮解は著しく進み難く、またこの長期保存物を用いたセメントペースト、モルタル又はコンクリートは、潮解等の風化が起こっていないアルカリ金属塩を配合使用した時と概ね遜色のない凝結性や強度発現性を呈したことから本発明を完成させた。 As a result of intensive studies for solving the problems, the inventor of the present invention uses any one of non-deliquescent inorganic powders among materials used in cement paste, mortar, concrete, etc. together with alkali metal salts, or By selecting two or more types, making the particle size of the selected inorganic powder fine, and using a filler in which an alkali metal salt is dispersed, a normal storage method according to the storage of the inorganic powder, For example, even when stored for a long period of 100 days or longer, the liquefaction of the alkali metal salt hardly progresses, and the cement paste, mortar, or concrete using the long-term stored product should be free of alkali metal salt that has not been weathered such as deliquescence. The present invention was completed from the fact that it exhibited a coagulation property and strength development that were almost the same as when blended and used.
即ち、本発明は次の（１）〜（３）で表されるアルカリ金属塩の風化防止方法である。（１）セメントペースト、モルタル又はコンクリートに使用するアルカリ金属塩の風化防止方法であって、該セメントペースト、モルタル又はコンクリートに使用される非潮解質無機粉末の何れか１種又は２種以上を平均粒径２０μｍ未満であって２０μｍを超える粒子含有率を２５質量％未満にし、この非潮解質無機粉末中にアルカリ金属塩を分散させて充填体にせしめることを特徴とするアルカリ金属塩の風化防止方法。（２）アルカリ金属塩を分散させる非潮解質無機粉末が、分散させるアルカリ金属塩１００体積部に対し、５００体積部以上の体積であることを特徴とする前記（１）のアルカリ金属塩の風化防止方法。（３）充填体の空隙率が６５体積％未満であることを特徴とする前記（１）又は（２）のアルカリ金属塩の風化防止方法。 That is, this invention is the weathering prevention method of the alkali metal salt represented by following (1)-(3). (1) Alkali metal salt weathering prevention method used for cement paste, mortar or concrete, average one or more of non-deliquescent inorganic powder used for cement paste, mortar or concrete Prevention of weathering of alkali metal salt, characterized in that the particle content is less than 20 μm and the particle content exceeds 20 μm is less than 25% by mass, and the alkali metal salt is dispersed in the non-deliquescent inorganic powder to form a filler. Method. (2) The weathering of alkali metal salt according to (1), wherein the non-deliquescent inorganic powder for dispersing the alkali metal salt has a volume of 500 parts by volume or more with respect to 100 parts by volume of the alkali metal salt to be dispersed. Prevention method. (3) The alkali metal salt weathering prevention method according to (1) or (2), wherein the porosity of the filler is less than 65% by volume.
本発明によれば、高い潮解性の故、変質し易いアルカリ金属塩を、長期間保存しても安定した凝結調整能力を発現させることができ、しかも本発明の風化防止方法は特別な容器や手間のかかる処理を必要としないため容易に遂行でき、従来法に比べ製造コストの上昇も抑えることが出来る。また、本法は特に、プレミックス（予混合）タイプのセメントペースト、モルタル又はコンクリート粉体組成物を製造する上では最適な手法として活用できる。 According to the present invention, due to high deliquescence, an alkali metal salt that is easily denatured can exhibit stable setting control ability even if stored for a long period of time, and the weathering prevention method of the present invention is a special container or Since a time-consuming process is not required, it can be easily performed, and an increase in manufacturing cost can be suppressed as compared with the conventional method. In addition, this method can be used as an optimum method particularly for producing a premix (premixed) type cement paste, mortar or concrete powder composition.
本発明のアルカリ金属塩の風化防止方法で対象とするアルカリ金属塩は、何れもセメントペースト、モルタル又はコンクリートで使用できものであって、多少とも潮解性を有するものであれば何れのものでも良い。具体的には、リチウム、カリウム、ナトリウムの、炭酸塩、硫酸塩、珪酸塩、アルミン酸塩、硝酸塩、亜硝酸塩の無機化合物の他、リチウム、カリウム、ナトリウムの、蟻酸塩、クエン酸塩、酒石酸塩、ヘプトン酸塩、グルコン酸塩、リン酸塩、硼酸塩等の有機化合物を例示することができる。 Any alkali metal salt targeted by the alkali metal salt weathering prevention method of the present invention can be used in cement paste, mortar, or concrete, and any liquefaction can be used. . Specifically, lithium, potassium, sodium carbonate, sulfate, silicate, aluminate, nitrate, nitrite inorganic compounds, lithium, potassium, sodium, formate, citrate, tartaric acid Examples thereof include organic compounds such as salts, heptonic acid salts, gluconic acid salts, phosphoric acid salts, and boric acid salts.
本発明では、前記のアルカリ金属塩を配合使用するセメントペースト、モルタル又はコンクリートで使用される他の成分のうち、非潮解質無機粉末にアルカリ金属塩を分散させるが、この無機粉末は潮解性が実質無い限り成分的には特に限定されず、その中の任意の１種又は２種以上を選定することができる。具体的には、例えばセメントを挙げることができ、セメントは何れの種類のものでも良い。セメント以外にも、例えば石英、コランダム（α−アルミナ）、カルサイト、石炭灰、スラグ、シリカフューム等の何れか１種を含むものでは、これをアルカリ金属塩を分散可能な非潮解質無機粉末として例示できる。好ましくは、水和反応活性ができるだけ低い無機粉末が良い。また、このような非潮解質無機粉末は、平均粒径２０μｍ未満であって２０μｍを超える粒子含有率を２５質量％未満（０質量％を含む。）の粒子を使用する。平均粒径２０μｍを超える粒子の使用では、アルカリ金属塩を分散させた混合粒子を充填しても、粒子間隙が大きくなり過ぎる可能性があり、該間隙が表面と連通することで外部の湿分が容易に混合粒子充填体の内部まで達し、アルカリ金属塩粒子の潮解化の進行を抑制し難くなるので好ましくない。また、２０μｍを超える粒子含有率が２５質量％を超える非潮解質無機粉末でも、粒子間隙が大きくなり過ぎて前記と同様の結果をもたらすことがあるので好ましくない。 In the present invention, among the other components used in cement paste, mortar or concrete containing the above alkali metal salt, the alkali metal salt is dispersed in the non-deliquescent inorganic powder, but this inorganic powder has deliquescence. As long as there is not substantially, it does not specifically limit for a component, Arbitrary 1 type (s) or 2 or more types can be selected in it. Specifically, for example, cement can be mentioned, and the cement may be any kind. In addition to cement, for example, those containing any one of quartz, corundum (α-alumina), calcite, coal ash, slag, silica fume, etc. are used as non-deliquescent inorganic powder capable of dispersing an alkali metal salt. It can be illustrated. Preferably, an inorganic powder having as low a hydration reaction activity as possible is preferable. Further, such non-deliquescent inorganic powder uses particles having an average particle size of less than 20 μm and a particle content exceeding 20 μm of less than 25 mass% (including 0 mass%). When particles having an average particle diameter of more than 20 μm are used, even if the mixed particles in which the alkali metal salt is dispersed are filled, there is a possibility that the particle gap may become too large. However, it is not preferable because it easily reaches the inside of the mixed particle filler and it is difficult to suppress the progress of liquefaction of the alkali metal salt particles. In addition, even non-deliquescent inorganic powders having a particle content exceeding 20 μm and exceeding 25% by mass are not preferable because the particle gaps may become too large, resulting in the same results as described above.
本発明では、アルカリ金属塩を前記の非潮解質無機粉末中に分散させ、この分散させてなる混合粒子を充填体にして保存に供する。分散方法は何等限定されず、例えば通常の乾式混合方法で行うことができる。また、アルカリ金属塩を分散させるために必要な非潮解質無機粉末の量は、アルカリ金属塩１００体積部に対し、非潮解質無機粉末５００体積部以上とする。非潮解質無機粉末５００体積部未満では充填体外表面に露呈するアルカリ金属塩の割合が多くなり、風化抑制を行い難くなることがあるので適当ではない。また、非潮解質無機粉末の上限量は制限されない。 In the present invention, the alkali metal salt is dispersed in the non-deliquescent inorganic powder, and the mixed particles obtained by the dispersion are used as a packing material for storage. The dispersion method is not limited at all, and for example, it can be carried out by a normal dry mixing method. In addition, the amount of the non-deliquescent inorganic powder necessary for dispersing the alkali metal salt is 500 parts by volume or more of the non-deliquescent inorganic powder with respect to 100 parts by volume of the alkali metal salt. If it is less than 500 parts by volume of the non-deliquescent inorganic powder, the proportion of the alkali metal salt exposed on the outer surface of the filler is increased, and it is difficult to suppress weathering. Further, the upper limit amount of the non-deliquescent inorganic powder is not limited.
また、充填体は、所定の容器や袋に混合粒子を充填させた状態のものでも混合粒子を所望の形状に成形した成形物の何れでも良い。ここで容器や袋は非透水性材質からなるものが望ましいが、これに限定されず、例えば市販のセメントの梱包に使用されている紙製袋でも可能である。混合粒子から充填体を得る方法は、特に限定されず、例えば金型に混合粒子を投入し、これを加圧して成形物にする方法、保存用の容器や袋に振動をかけながら混合粒子を投入充填する方法、混合粒子の粒度を更に調整し、細密構造を得やすいような粒度分布、例えば２μｍ未満、２〜５μｍ、５〜１０μｍ、１０〜２０μｍ、２０〜３０μｍ、３０μｍ超に区分の上、これらの粒子群が概ね均等質量となるような分布に調整し、これを容器や袋に投入する方法等を挙げることができる。充填体は、空隙率が６５体積％未満のものとするのが好ましい。６５体積％を超えると、粒子間隙が大きくなり充填体内部まで外気が入り易く、風化抑制が困難となることがあるので適当ではない。 The filling body may be either a state in which a predetermined container or bag is filled with mixed particles or a molded product obtained by forming mixed particles into a desired shape. Here, the container or bag is preferably made of a water-impermeable material, but is not limited to this, and for example, a paper bag used for packing cement on the market is also possible. The method for obtaining the filler from the mixed particles is not particularly limited. For example, the mixed particles are put into a mold and pressed to form a molded product, and the mixed particles are shaken while vibrating a storage container or bag. The method of charging and filling, further adjusting the particle size of the mixed particles, particle size distribution that makes it easy to obtain a fine structure, for example, less than 2 μm, 2-5 μm, 5-10 μm, 10-20 μm, 20-30 μm, over 30 μm And a method of adjusting the distribution so that these particle groups have a substantially uniform mass and putting them in a container or bag. The filler preferably has a porosity of less than 65% by volume. If it exceeds 65% by volume, the interstices between the particles become large and the outside air tends to enter the inside of the packed body, which makes it difficult to suppress weathering.
このようにして得た充填体は、成形物なら例えばそのまま又はビニール等に入れて保存でき、また容器や袋に入れて充填体としたものは脱気等の処理を行わなくてもそのまま保存できる。保存場所は特に制限されず、例えば、恒温環境に保たれた屋内でも外気が通気する倉庫等でも良い。 The filler thus obtained can be stored as it is, for example, as it is in a molded article or in vinyl or the like, and the filler in a container or bag can be stored as it is without performing degassing or the like. . The storage location is not particularly limited, and may be, for example, an indoor room kept in a constant temperature environment or a warehouse where outside air is ventilated.
以下に記すアルカリ金属塩（Ａ１〜Ａ４）の何れか１種２質量部、以下に記すカルサイト、コランダム、アルミナセメント又は早強ポルトランドセメントの無機粉末（Ｂ１〜Ｂ６）の何れか１種４８質量部、普通ポルトランドセメント４００質量部、細骨材（ＪＩＳ Ｒ５２０１「セメントの強さ試験用標準砂」で規定された砂）１３５０質量部及び水２２５質量部からなるモルタル組成物を製造する前作業として、表１に表す配合となるようカルサイト、コランダム又はアルミナセメントの無機粉末の何れか１種とアルカリ金属塩をレーディゲミキサに投入し、約３分間乾式混合して混合粒子を作製した。 48 parts by mass of any one of the following alkali metal salts (A1 to A4), 2 parts by mass of any one of the following inorganic powders (B1 to B6) of calcite, corundum, alumina cement or early strong Portland cement As a preparatory work for producing a mortar composition comprising 1 part by weight, 400 parts by weight of ordinary Portland cement, 1350 parts by weight of fine aggregate (sand defined in JIS R5201 “Standard sand for cement strength test”) and 225 parts by weight of water One of calcite, corundum, or alumina cement inorganic powder and an alkali metal salt were put into a Laedige mixer so as to have the composition shown in Table 1, and dry mixed for about 3 minutes to prepare mixed particles.
Ａ１；炭酸ナトリウム（凝結促進用、平均粒径５０μｍ）
Ａ２；硫酸カリウム（凝結促進用、平均粒径５０μｍ）
Ａ３；クエン酸ナトリウム（凝結遅延用、平均粒径５０μｍ）
Ａ４；ロッシェル塩（凝結遅延用、平均粒径５０μｍ）
Ｂ１；カルサイト（平均粒径６μｍ、２０μｍ超の粒子含有率１４質量％）
Ｂ２；カルサイト（平均粒径１５μｍ、２０μｍ超の粒子含有率４１質量％）
Ｂ３；カルサイト（平均粒径５μｍ、２０μｍ超の粒子含有率０質量％）
Ｂ４；コランダム（平均粒径４５μｍ、２０μｍ超の粒子含有率８０質量％）
Ｂ５；アルミナセメント（平均粒径７μｍ、２０μｍ超の粒子含有率１８質量％）
Ｂ６；早強ポルトランドセメント（平均粒径８μｍ、２０μｍ超の粒子含有率１５質量％）
A1; sodium carbonate (for condensing promotion, average particle size 50 μm)
A2: Potassium sulfate (for condensing promotion, average particle size 50 μm)
A3: Sodium citrate (for setting delay, average particle size 50 μm)
A4: Rochelle salt (for setting delay, average particle size 50 μm)
B1: Calcite (average particle size 6 μm, content of particles exceeding 20 μm 14 mass%)
B2: Calcite (average particle size 15 μm, particle content 41 mass% over 20 μm)
B3: Calcite (average particle size of 5 μm, content of particles exceeding 20 μm 0 mass%)
B4: Corundum (average particle size 45 μm, particle content of more than 20 μm 80 mass%)
B5: Alumina cement (average particle size 7 μm, particle content of more than 20 μm 18 mass%)
B6: Early strength Portland cement (average particle size 8 μm, content of particles exceeding 20 μm 15 mass%)
得られた混合粒子を用い、ＪＩＳ Ａ１１０４に準じたジッギング法によって充填し、充填体を作製した。その際、充填物の充填率はジッギング回数により調整した。表１にはその結果も表す。 The obtained mixed particles were filled by a jigging method according to JIS A1104 to prepare a filled body. At that time, the filling rate of the packing was adjusted by the number of times of jigging. Table 1 also shows the results.
作製した充填体はジッギング処理直後の未梱包の状態で、温度２０℃、湿度６０％の恒温恒湿の屋内に半年間保存した。保存後の充填体は、潮解による変質が発生しているか否かを目視による表面状態の変化によって調べ、充填体作製直後の表面と比較して表面の一部でも液状化が見られたものを変質「有り」と判断し、概ね充填体作製直後の表面状態を保っていたものを変質「無し」と判断した。この結果を表１に表す。 The produced filling body was stored in a non-packed state immediately after the jigging process in a room of constant temperature and humidity at a temperature of 20 ° C. and a humidity of 60% for half a year. After the storage, the packed body is examined by visual changes in the surface condition to determine whether or not alteration due to deliquescence has occurred. It was judged that the alteration was “present”, and the surface state almost immediately after the production of the filling body was judged as “no alteration”. The results are shown in Table 1.
次いで、保存期間を設けないジッギング処理直後の充填体及び半年間保存した充填体を用い、前記配合のモルタル組成物をホバートミキサで製造した。混練直後のモルタル組成物を使用し、４×４×１６ｃｍの成形体を型枠成形により作製した。成形体は気中養生２４時間後に脱型したものを、さらに材齢２８日まで２０℃の水中で養生した。所望される凝結特性に応じて脱型直後の成形体（材齢１日）又は水中養生後の成形体（材齢２８日）の圧縮強度を、ＪＩＳ Ｒ２５２１に準じた方法により測定した。その結果を表２に表す。 Next, a mortar composition having the above-mentioned composition was produced with a Hobart mixer using a packing immediately after the jigging process without a storage period and a packing stored for six months. Using a mortar composition immediately after kneading, a molded body of 4 × 4 × 16 cm was prepared by molding. The molded body was demolded after 24 hours in the air and further cured in water at 20 ° C. until the age of 28 days. Depending on the desired setting characteristics, the compressive strength of the molded body immediately after demolding (age 1 day) or the molded body after water curing (material age 28 days) was measured by a method according to JIS R2521. The results are shown in Table 2.
表２から、本発明による方法で得た充填体は、通常の保管方法で半年間保管しても、潮解は実質起こらず、またこの充填体を配合使用したモルタル組成物は、保存期間のない作製直後の充填体を配合使用したモルタル組成物と比べ、何れも遜色ない早期強度発現性（実施例１〜３及び６）又は長期強度発現性（実施例４〜５）を呈し、凝結性に作用するアルカリ金属塩の本来の性質が変化無く維持できていることがわかる。これに対し本発明によらないアルカリ金属塩の保存方法で得た充填体を配合使用したモルタル組成物は、保存期間のない作製直後の充填体を配合使用したモルタル組成物と比べて、所望の早期強度強度発現性（比較例８）又は長期強度発現性（比較例７）が得られず、風化によって金属アルカリ塩の凝結性に及ぼす作用能力の低下が生じたことが窺える。 From Table 2, the packing obtained by the method according to the present invention does not cause deliquescence substantially even when stored for 6 months by a normal storage method, and the mortar composition using this packing does not have a storage period. Compared to a mortar composition containing and blended with a filler immediately after production, it exhibits inferior early strength development (Examples 1 to 3 and 6) or long-term strength development (Examples 4 to 5). It can be seen that the original properties of the acting alkali metal salt can be maintained without change. On the other hand, the mortar composition using the filler obtained by the alkali metal salt preservation method not according to the present invention is more desirable than the mortar composition containing the filler immediately after production without storage period. The early strength development (Comparative Example 8) or the long-term strength development (Comparative Example 7) could not be obtained, and it seems that the ability to affect the coagulability of the metal alkali salt was reduced by weathering.
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| JPH08169739A (en) * | 1994-12-16 | 1996-07-02 | M & Ii Kk | Admixture for concrete exposed to low temperature |
| JP2000233959A (en) * | 1999-02-10 | 2000-08-29 | Taiheiyo Cement Corp | Clinker ground material, high-early-strength cement composition containing the same, concrete and concrete product |
| JP2002308657A (en) * | 2001-02-09 | 2002-10-23 | Mitsubishi Materials Corp | Quick-hardening admixture and quick-hardening lightweight joint mortar |
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| JPS63123848A (en) * | 1986-11-10 | 1988-05-27 | 麻生セメント株式会社 | Admixing agent for preparing suspension for cement milk process |
| JPH08169739A (en) * | 1994-12-16 | 1996-07-02 | M & Ii Kk | Admixture for concrete exposed to low temperature |
| JP2000233959A (en) * | 1999-02-10 | 2000-08-29 | Taiheiyo Cement Corp | Clinker ground material, high-early-strength cement composition containing the same, concrete and concrete product |
| JP2002308657A (en) * | 2001-02-09 | 2002-10-23 | Mitsubishi Materials Corp | Quick-hardening admixture and quick-hardening lightweight joint mortar |
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