JPH0415273B2 - - Google Patents
Info
- Publication number
- JPH0415273B2 JPH0415273B2 JP62106376A JP10637687A JPH0415273B2 JP H0415273 B2 JPH0415273 B2 JP H0415273B2 JP 62106376 A JP62106376 A JP 62106376A JP 10637687 A JP10637687 A JP 10637687A JP H0415273 B2 JPH0415273 B2 JP H0415273B2
- Authority
- JP
- Japan
- Prior art keywords
- liquid
- injection method
- setting
- salt
- calcium
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000007788 liquid Substances 0.000 claims description 29
- 239000003795 chemical substances by application Substances 0.000 claims description 16
- 238000002347 injection Methods 0.000 claims description 15
- 239000007924 injection Substances 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 14
- 150000003839 salts Chemical class 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical class O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 9
- 239000011440 grout Substances 0.000 claims description 9
- 238000002156 mixing Methods 0.000 claims description 9
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 8
- 229910052791 calcium Inorganic materials 0.000 claims description 8
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 8
- 239000004568 cement Substances 0.000 claims description 7
- 239000002893 slag Substances 0.000 claims description 6
- 239000010440 gypsum Substances 0.000 claims description 5
- 229910052602 gypsum Inorganic materials 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- 229910000027 potassium carbonate Inorganic materials 0.000 claims description 4
- 239000000377 silicon dioxide Substances 0.000 claims description 4
- -1 Ca or Mg Chemical class 0.000 claims description 3
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims description 3
- 239000000920 calcium hydroxide Substances 0.000 claims description 3
- 235000011116 calcium hydroxide Nutrition 0.000 claims description 3
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims description 3
- 230000007935 neutral effect Effects 0.000 claims description 3
- 239000000243 solution Substances 0.000 claims description 3
- 239000010881 fly ash Substances 0.000 claims description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 claims 1
- 159000000007 calcium salts Chemical class 0.000 description 14
- 238000001879 gelation Methods 0.000 description 10
- 235000010469 Glycine max Nutrition 0.000 description 8
- 244000068988 Glycine max Species 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 7
- 239000011575 calcium Substances 0.000 description 7
- 238000004898 kneading Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000002002 slurry Substances 0.000 description 5
- 150000004645 aluminates Chemical class 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 159000000003 magnesium salts Chemical class 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 235000010755 mineral Nutrition 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- MXRIRQGCELJRSN-UHFFFAOYSA-N O.O.O.[Al] Chemical compound O.O.O.[Al] MXRIRQGCELJRSN-UHFFFAOYSA-N 0.000 description 2
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
- 244000046052 Phaseolus vulgaris Species 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- XFWJKVMFIVXPKK-UHFFFAOYSA-N calcium;oxido(oxo)alumane Chemical compound [Ca+2].[O-][Al]=O.[O-][Al]=O XFWJKVMFIVXPKK-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 229910001653 ettringite Inorganic materials 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VBUYCZFBVCCYFD-JJYYJPOSSA-N 2-dehydro-D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C(=O)C(O)=O VBUYCZFBVCCYFD-JJYYJPOSSA-N 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- 239000011398 Portland cement Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 229940037003 alum Drugs 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
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 1
- 229910052925 anhydrite Inorganic materials 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000004567 concrete Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 229910001388 sodium aluminate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
- C04B28/02—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
- C04B28/06—Aluminous cements
- C04B28/065—Calcium aluminosulfate cements, e.g. cements hydrating into ettringite
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Soil Conditioners And Soil-Stabilizing Materials (AREA)
- Consolidation Of Soil By Introduction Of Solidifying Substances Into Soil (AREA)
Description
【発明の詳細な説明】
<産業上の利用分野>
本発明は、構造物基礎岩盤あるいはコンクリー
ト構造物と地山の間隙等を填充する、グラウト注
入方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a grout injection method for filling a gap between a foundation rock of a structure or a concrete structure and the ground.
<従来の技術>
グラウト注入材を注入する際において、注入材
が硬化する時間、すなわちゲルタイムを正確に得
ることが望ましい。<Prior Art> When injecting a grout injection material, it is desirable to accurately obtain the time for the injection material to harden, that is, the gel time.
そこで現在のセメント系超速硬性注入材の注入
方法は次のようになる。 Therefore, the current injection method for cement-based ultra-fast hardening injection materials is as follows.
まずカルシウムやアルミネート系鉱物を主成分
とする急結剤に、石膏および重炭酸塩、炭酸塩等
の凝結遅延剤を加えたものをB液とする。 First, liquid B is prepared by adding gypsum and a setting retardant such as bicarbonate or carbonate to a rapid setting agent mainly composed of calcium or aluminate minerals.
次に、地盤に注入する前に、B液とセメント
(A液)とを撹拌あるいは混合させる。 Next, before pouring into the ground, liquid B and cement (liquid A) are stirred or mixed.
その後、地盤に注入し、エトリンガイド(カル
シウム、サルフオ・アルミネート)を生成し、急
結させるいうものである。 After that, it is injected into the ground to generate Etrin guide (calcium, sulfur aluminate) and cause it to set quickly.
<発明が解決しようとする問題点>
前記した従来のグラウト注入技術には、次のよ
うな問題点が存在する。<Problems to be Solved by the Invention> The conventional grout injection techniques described above have the following problems.
B液のカルシウム、アルミネート系急結剤は、
カルシウム塩を含有しており、またそれらは容易
にイオン化しやすい。 Calcium and aluminate quick-setting agent of B liquid are:
They contain calcium salts and are easily ionized.
そのため、地盤に注入する前に、B液を撹拌、
混練(ミキシング、アジテーテイング)しておく
と、カルシウム塩と凝結遅延剤とが反応して、凝
結遅延剤としての量が減少してしまう。 Therefore, before injecting into the ground, stir the B liquid.
If kneaded (mixing, agitating), the calcium salt and the setting retarder will react and the amount of the setting retarder will decrease.
その結果、A,B二液混合時に、当初計画通り
の遅延剤の量が確保されないため、ゲルタイムが
混練時間によつて変動してしまう。 As a result, when mixing the two liquids A and B, the amount of retardant as originally planned cannot be secured, so the gel time varies depending on the kneading time.
しかし、カルシウム、アルミネート系急結剤
は、カルシウム系鉱物とアルミニウム系鉱物とを
溶融させて製造する溶融生成物等が用いられてい
るから、これをカルシウム塩とその他のものに分
離することは、不可能である。 However, calcium and aluminate-based quick-setting agents use melted products produced by melting calcium-based minerals and aluminum-based minerals, so it is impossible to separate them into calcium salts and other substances. , is impossible.
したがつて、セメント系超速硬性注入材におい
て、今までは、ゲルタイムの変動は避けられなか
つた。 Therefore, until now, fluctuations in gel time have been unavoidable in cement-based ultra-fast hardening injection materials.
<本発明の目的>
本発明は上記のような問題点を解決するため、
次のようなグラウト注入方法を提供することを目
的とする。<Object of the present invention> In order to solve the above-mentioned problems, the present invention has the following objectives:
The purpose is to provide a grouting method as follows.
B液側に含有されているカルシウム塩と凝結遅
延剤との反応による凝結遅延剤の減少を防止し、
ゲルタイムにほとんど変動を与ないで地盤に注入
することができる、グラウト注入方法。 Preventing the reduction of the setting retarder due to the reaction between the calcium salt contained in the B liquid side and the setting retarder,
A grout injection method that allows grout to be injected into the ground with almost no change in gel time.
<本発明の構成>
以下、図面を参照しなながら本発明の一実施例
について説明する。<Configuration of the Present Invention> An embodiment of the present invention will be described below with reference to the drawings.
(イ) A液組成
A液は、カルシウム塩を主生分とした材料、た
とえば、セメント、石灰、石膏の混合物から成
る。(a) Composition of liquid A Liquid A consists of a mixture of materials whose main constituents are calcium salts, such as cement, lime, and gypsum.
(ロ) B液組成
B液は、活性アルミナ塩系急結剤と凝結遅延剤
から成る。(b) Composition of B liquid B liquid consists of an activated alumina salt quick setting agent and a setting retarder.
(1) 活性アルミナ塩系急結剤
注入材のように非常に水分が多い材料(一般
に、W/C≧100%、W=水、C=セメント、急
結材等の固形分)を混合して、数分以内にゲル化
させる方法としては、セメントを主剤とする場合
には、水和生成物としてエトリンガイト(3CaO、
Al2O3・3CaSO4、nH2O)を作る必要がある。(1) Activated alumina salt-based quick-setting agent This agent is used to mix materials with extremely high water content such as injection materials (generally W/C≧100%, W = water, C = solid content such as cement, quick-setting materials, etc.). In order to achieve gelation within a few minutes, when cement is used as the main ingredient, ettringite (3CaO,
It is necessary to make Al 2 O 3・3CaSO 4 , nH 2 O).
このエトリンガイトを作るためには、カルシウ
ムアルミネートと石膏、あるいは消石灰、または
石膏と活性アルミナ塩が必要である。 To make this ettringite, calcium aluminate and gypsum, or slaked lime, or gypsum and activated alumina salts are required.
本発明では、急結剤に含有されるカルシウム塩
と凝結遅延剤とが、混練時間と共に反応して、凝
結遅延剤の量が減少し、ゲルタイムに影響を及ぼ
すことを防止するため、カルシウム塩とアルミナ
塩を分散する目的で、活性アルミナ塩を用いる。 In the present invention, in order to prevent the calcium salt contained in the accelerating agent from reacting with the setting retarder over kneading time, reducing the amount of the setting retarder and affecting the gel time, the calcium salt and the setting retarder are Activated alumina salt is used for the purpose of dispersing the alumina salt.
活性アルミナ塩系急結剤としては、例えば、仮
焼みようばん、アルサイト(非晶質アルミナ)お
よび、これらの混合物、またはこれに微量のカリ
みようばん、アルミン酸ソーダを添加したものを
使用する。 As the activated alumina salt quick-setting agent, for example, calcined soybean, alcite (amorphous alumina), a mixture thereof, or a mixture thereof with a trace amount of potassium soybean or sodium aluminate added thereto can be used. .
一例として、仮焼みようばんと、アルサイト
(非晶質アルミナ)の成分を第1図の表に示す。 As an example, the components of calcined soybean paste and alcite (amorphous alumina) are shown in the table of FIG.
仮焼みようばんは、加里みようばんを650℃で
焼成したもので、次の化学式で与えられる。 Calcined soybean is made by firing Kari soybean at 650℃ and is given by the following chemical formula.
加里みようばん 仮焼みようばん
K2O・3Al2O3・4SO3・6H2O→Al2(SO4)3K2
SO4+2Al2O3+H2O
650℃ (無定形)
尚、第1図に示した仮焼みようばんは、みよう
ばん石を500℃で焼いたものであり、上式の仮焼
みようばんと組成が相違するが、両者の化学反応
力はほとんど同じである。 Kari miyouban Temporarily baked miyouban K 2 O・3Al 2 O 3・4SO 3・6H 2 O→Al 2 (SO 4 ) 3 K 2
SO 4 +2Al 2 O 3 +H 2 O 650℃ (amorphous) The calcined sour bean shown in Fig. 1 is made by baking alum stone at 500℃, and is different from the calcined sour bean in the above formula. Although their compositions are different, their chemical reaction power is almost the same.
(2) 凝結遅延剤
凝結遅延剤としては、例えば、炭酸ソーダー、
炭酸カリ、重炭酸ソーダー、および2ケトルグル
コン酸、クエン酸等を混合した、カルシウム塩、
マグネシウム塩等の2価金属塩を含まないものを
使用する。(2) Setting retarder Examples of setting retarders include soda carbonate,
Calcium salt, a mixture of potassium carbonate, bicarbonate of soda, and 2 kettle gluconic acid, citric acid, etc.
Use one that does not contain divalent metal salts such as magnesium salts.
仮焼みようばんやアルサイトなどは、カルシウ
ム塩、マグネシウム塩が非常に少なく、上記遅延
剤を混合、撹拌しても、ゲルタイムにはほとんど
影響を与えない。 Calculated soybean paste and alcite contain very little calcium salt and magnesium salt, so even if the retarder is mixed and stirred, the gel time is hardly affected.
(ハ) その他の実施例
(1) B液にシリカの純度が非常に高い超微粒子の
シリカヒユーム等の、活性シリカ粉末を加える
と、無添加のものに比較して、ゲル化特性の改
善(ゲル開始から固化反応までの、粘度上昇が
急になる)がみられる。(c) Other Examples (1) When active silica powder such as ultrafine silica hume with extremely high silica purity is added to liquid B, the gelation properties are improved (gel A sharp increase in viscosity is observed from the start of the reaction to the solidification reaction.
また、これらを加えても、2価金属塩を含ん
でいないため、混練時間によるゲル化タイムの
変動に対して、ほとんど影響がない。 Further, even if these are added, since they do not contain divalent metal salts, they have almost no effect on the variation in gelation time due to kneading time.
(2) B液側の材料のPHがほぼ中性であるとき、
高炉スラグ、フライアツシユ等のポゾラン材を
B液側に加えることにより、両液の粘性調整、
凝固後の長期安定性向上を計ることができる。(2) When the pH of the material on the B liquid side is almost neutral,
By adding pozzolanic materials such as blast furnace slag and fly ash to the B liquid side, the viscosity of both liquids can be adjusted.
It is possible to measure the long-term stability improvement after solidification.
つまり、たとえば高炉スラグは、その中にカ
ルウム塩が含まれており、アルカリ溶液中では
自硬性がありカルシウム塩のイオン化が激しい
が、中性域では遅い。 That is, for example, blast furnace slag contains calcium salts, and is self-hardening in an alkaline solution, and ionization of the calcium salts is intense, but it is slow in the neutral range.
したがつて、B液側に高炉スラグを添加する
と、多少のゲルタイムの変動があるものの、色
の反応速度が遅いことにより、ゲルタイムの変
動を多少許容するような場合では、B液側に添
加することができる。 Therefore, if blast furnace slag is added to the B liquid side, there will be some variation in the gel time, but in cases where some variation in the gel time is acceptable due to the slow reaction rate of the color, adding blast furnace slag to the B liquid side is recommended. be able to.
なお、W/Cが大きい場合、高炉スラグを添
加すると、1〜4週強度は著しく改善できるこ
とから、多少のゲルタイムの変動が許容できる
ところへの適用には、重要な意義をもつてい
る。 In addition, when the W/C is large, the 1-4 week strength can be significantly improved by adding blast furnace slag, so it has important significance in applications where some variation in gel time is acceptable.
(ホ) 比較例
(1) 従来技術
ポルランドセメント300g、水400c.c.を混合、撹
拌したスラリーをA液とし、カルシウム、アルミ
ニウムシリケート系急結剤75g、水475c.c.を混入
したスラリーをB液とする。(e) Comparative example (1) Prior art Liquid A is a slurry made by mixing and stirring 300 g of Portland cement and 400 c.c. of water, and a slurry in which calcium, 75 g of an aluminum silicate quick-setting agent, and 475 c.c. of water are mixed. is called liquid B.
そして、B液側に炭酸カリとクエン酸系遅延剤
1.25g、あるいは1g添加した材料を各液とも10
〜60分混練し、各1時間毎にA,B両液を混し、
ゲル化タイムを回転粘度計を用いて測定した。 Then, on the B liquid side, potassium carbonate and citric acid retardant.
1.25g or 1g of added material for each solution
Knead for ~60 minutes, mixing both solutions A and B every hour.
Gelation time was measured using a rotational viscometer.
第2図は、横軸に混練時間を、縦軸にゲル化タ
イムを示し、・印は遅延剤が1.25gの場合を、×印
は遅延剤が1gの場合を示している。 In FIG. 2, the horizontal axis shows the kneading time, and the vertical axis shows the gelation time, and the mark "*" shows the case where the retarder is 1.25 g, and the "X" shows the case where the retarder is 1 g.
この図から、各遅延剤量の場合とも混練時間が
長くなるにしたがつて、ゲル化タイムは短くなる
ことがわかる。 From this figure, it can be seen that for each retarder amount, as the kneading time becomes longer, the gelation time becomes shorter.
このことから、カルシウム、アルミネート系急
結剤と遅延剤とが徐々に反応し、ゲル化時間は遅
延材料だけでなく、混練時間にも影響を受けるこ
とが分かる。 From this, it can be seen that the calcium and aluminate-based quick-setting agent and the retarder gradually react, and the gelation time is affected not only by the retarder material but also by the kneading time.
(2) 本発明の技術
ポルトランド246g、消石灰21.4g、無水石膏
49.2g、水393.4gを混合、撹拌したスラリーを
A液とし、仮焼みようばん、アルサイト混合急結
剤を18.5g、2ケトグルコン酸および炭酸カリ混
合遅延剤を44.5g、水を476.3gを混合、撹拌し
たスラリーをB液とする。(2) Technology of the present invention Portland 246g, slaked lime 21.4g, anhydrite
Mix and stir 49.2g of 49.2g of water and 393.4g of water to make the slurry A liquid, add 18.5g of calcined soybean paste, 18.5g of alcite mixed quick setting agent, 44.5g of 2-ketogluconic acid and potassium carbonate mixed retardant, and 476.3g of water. The mixed and stirred slurry is referred to as liquid B.
各液を10〜80分混練し、各時間毎にA,B両液
を混合し、ゲル化タイムを回転粘度計を用いて測
定した。 Each liquid was kneaded for 10 to 80 minutes, and both liquids A and B were mixed at each time interval, and the gelation time was measured using a rotational viscometer.
第3図は、回転粘度計の粘度一時間の曲線記録
を、各時間毎に重ね合わせたものである。 FIG. 3 shows an hourly viscosity curve record of a rotational viscometer superimposed for each hour.
この図の縦軸は、粘度ηを表し、単位は、C・
P(センチポアーズ)である。 The vertical axis of this figure represents the viscosity η, and the unit is C·
P (centipoise).
また、横軸は、混合からの経過時間を示してい
る。 Moreover, the horizontal axis indicates the elapsed time from mixing.
この図から、いずれの混合時間のスラリーとも
混合後3分でゲル化が始まつており、カルシウム
塩、マグネシウム塩等の2価金属塩を含まない急
結剤と遅延剤は、混練時間によるゲル価時間の影
響は非常に小さいことを示している。 From this figure, gelation begins 3 minutes after mixing for slurries with any mixing time, and gelation occurs with rapid setting agents and retarders that do not contain divalent metal salts such as calcium salts and magnesium salts depending on the mixing time. This shows that the effect of valence time is very small.
本発明は、この現象を見出し、注入工法に応用
したものである。 The present invention discovered this phenomenon and applied it to the injection method.
<本発明の効果>
本発明は以上説明したようになるので、次のよ
うな効果を期待するこができる。<Effects of the Present Invention> Since the present invention has been described above, the following effects can be expected.
凝結遅延剤カルシウム・アルミネート系急結剤
を混練した場合、その混練時間によつて、凝結遅
延剤と急結剤に含有されるカルシウム塩が反応
し、凝結遅延剤が減少して、ゲルタイムに変動を
与える。 Setting Retarder When a calcium aluminate-based quick setting agent is kneaded, the setting retarder reacts with the calcium salt contained in the quick setting agent depending on the kneading time, reducing the setting retarder and increasing the gel time. Give variation.
しかし、急結剤にカルシウム塩を含まない活性
アルミナ塩系急結剤を用いるこにより、上記のよ
うなゲルタイムの変動を防止するこができる。 However, by using an activated alumina salt-based quick-setting agent that does not contain calcium salts, the above-mentioned fluctuations in gel time can be prevented.
したがつて、注入材を地盤に注入する際に、正
確なゲルタイムを作り出すことができるので、よ
り良好なグラウト注入方法が可能となつた。 Therefore, since it is possible to create an accurate gel time when injecting the grouting material into the ground, a better grout injection method has become possible.
第1図:仮焼みようばんと、アルサイトの成分
表、第2図:従来技術のゲルタイム変化表、第3
図:本発明のゲルタイム変化表。
Figure 1: Table of ingredients for calcined soybean paste and alcite, Figure 2: Gel time change table of conventional technology, Figure 3
Figure: Gel time change table of the present invention.
Claims (1)
イムを調整するAB2液混合注入工法において、 セメント、消石灰または石膏からなる反応性2
価金属塩を主成分とするA液と、 CaやMgの2価金属塩を含まない活性アルミナ
塩系急結剤と炭酸カリまたは炭酸ソーダ有機酸塩
の凝結遅延剤とからなるB液を用いることを特徴
とする、 グラウト注入方法。 2 B液には、さらにシリカヒユームからなる活
性シリカを加えることを特徴とする、 特許請求の範囲第1項記載のグラウト注入方
法。 3 B液がほぼ中性であるときに高炉スラグやフ
ライアツシユからなるボゾラン材を、 B液に添加することを特徴とする、 特許請求の範囲第1項記載のグラウト注入方
法。[Claims] 1. In the AB2 liquid mixing injection method that adjusts the gel time by producing an Etrin guide, reactive 2 consisting of cement, slaked lime or gypsum.
Liquid A is mainly composed of a valent metal salt, and Liquid B is made of an active alumina salt quick setting agent that does not contain divalent metal salts such as Ca or Mg, and a setting retarder of potassium carbonate or sodium carbonate organic acid salt. A grout injection method characterized by: 2. The grout injection method according to claim 1, characterized in that activated silica consisting of silica hume is further added to the B solution. 3. The grout injection method according to claim 1, characterized in that a bozolan material made of blast furnace slag or fly ash is added to the B liquid when the B liquid is substantially neutral.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10637687A JPS63273689A (en) | 1987-05-01 | 1987-05-01 | Impregnation of grout |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10637687A JPS63273689A (en) | 1987-05-01 | 1987-05-01 | Impregnation of grout |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63273689A JPS63273689A (en) | 1988-11-10 |
JPH0415273B2 true JPH0415273B2 (en) | 1992-03-17 |
Family
ID=14431996
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10637687A Granted JPS63273689A (en) | 1987-05-01 | 1987-05-01 | Impregnation of grout |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63273689A (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006117887A (en) * | 2004-10-25 | 2006-05-11 | Raito Kogyo Co Ltd | Grout for foundation improvement |
KR100869467B1 (en) * | 2004-11-11 | 2008-11-19 | 덴끼 가가꾸 고교 가부시키가이샤 | Composition for ground-improving material, grouting material comprising the same, and method of using the same |
JP5620045B2 (en) * | 2007-12-28 | 2014-11-05 | 電気化学工業株式会社 | Injection material and injection method |
JP5916933B1 (en) * | 2015-10-16 | 2016-05-11 | 株式会社大阪防水建設社 | Two-component plastic grout material |
JP6818271B2 (en) * | 2016-09-06 | 2021-01-20 | 株式会社大林組 | Water-stopping method for water-stopping liquid mixing injection system, water-stopping liquid mixing injection plug and cement-based composition structure |
CN110272250A (en) * | 2019-07-02 | 2019-09-24 | 盖彦龙 | A kind of high fluidity cement concrete configuration method |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6162589A (en) * | 1984-09-04 | 1986-03-31 | Shimoda Gijutsu Kenkyusho:Kk | Backing grout material |
-
1987
- 1987-05-01 JP JP10637687A patent/JPS63273689A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6162589A (en) * | 1984-09-04 | 1986-03-31 | Shimoda Gijutsu Kenkyusho:Kk | Backing grout material |
Also Published As
Publication number | Publication date |
---|---|
JPS63273689A (en) | 1988-11-10 |
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