JPH0492013A - Ground grouting work - Google Patents
Ground grouting workInfo
- Publication number
- JPH0492013A JPH0492013A JP20804690A JP20804690A JPH0492013A JP H0492013 A JPH0492013 A JP H0492013A JP 20804690 A JP20804690 A JP 20804690A JP 20804690 A JP20804690 A JP 20804690A JP H0492013 A JPH0492013 A JP H0492013A
- Authority
- JP
- Japan
- Prior art keywords
- liquid
- soluble
- water glass
- ground
- reactant
- 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
Landscapes
- Consolidation Of Soil By Introduction Of Solidifying Substances Into Soil (AREA)
- Soil Conditioners And Soil-Stabilizing Materials (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は地盤中に特定の注入液を注入して地盤を固結す
る地盤注入工法に係り、詳細には注入液のゲル化時間調
整が容易で、かつ浸透性に優れた地盤注入工法に関する
。[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a ground injection method for solidifying the ground by injecting a specific injection liquid into the ground. This article relates to a ground injection method that is easy and has excellent permeability.
地盤固結用注入液として、従来、水ガラス水溶液に、無
機塩、有機塩あるいはグリオキザールやエステル類、さ
らにはセメント等を加えてゲル化せしめる水ガラスグラ
ウトが知られている。As an injection solution for ground consolidation, water glass grout is conventionally known, which is made by adding inorganic salts, organic salts, glyoxal, esters, cement, etc. to an aqueous water glass solution to form a gel.
上述において、無機塩として水溶性無機塩を用いたもの
はゲル化時間の調整にあたってわずかな無機塩量の違い
でゲル化時間が大幅に変化し、あるいはわずかに過少で
あるだ1・」で全くゲル化しないという現象が生じ、こ
のため固結が不確実であった。In the above, when a water-soluble inorganic salt is used as the inorganic salt, when adjusting the gelation time, a slight difference in the amount of inorganic salt causes a significant change in the gelation time, or a slight difference in the amount of the inorganic salt. A phenomenon in which gelation did not occur occurred, and caking was therefore uncertain.
また、難溶性無機塩やセメントの例では、浸透性が悪く
、さらには上述有機系の例では地下水のBODやCOD
を増加させるという問題があった。In addition, in the case of poorly soluble inorganic salts and cement, permeability is poor, and furthermore, in the above-mentioned organic examples, groundwater BOD and COD
There was a problem of increasing the
上述の8例において、特に水溶性無機塩を用いる場合、
このゲル化を確実に行い、かつゲル化時間の調整を容易
に行なえれば極めて有用な注入液となることが期待され
る。In the eight examples above, especially when using water-soluble inorganic salts,
If this gelation can be performed reliably and the gelation time can be easily adjusted, it is expected that an extremely useful injection solution will be produced.
そこで、この期待を実現するた酌に、3号水ガラスにあ
らかじめNaC1,、KCAあるいはアルカリ土金属塩
を混合したものをA液きし、他の反応剤水溶液をB液と
し、これらA、B液を組み合わせる注入工法が提案され
ている。しかし、3号水ガラスにNaCβ、KCAある
いはアルカリ土金属塩を混、合すると、混合液中にjロ
イドが急激に形成されるたy〕、A液を製造してからB
液等加えるまでの経過時間の違いによりゲル化時間が大
幅に異なり、ゲル化時間の調整がしにくいという問題が
あった。Therefore, in order to realize this expectation, we mixed No. 3 water glass with NaCl, KCA, or alkaline earth metal salts in advance as Solution A, and prepared an aqueous solution of other reactants as Solution B. An injection method that combines liquids has been proposed. However, when NaCβ, KCA, or alkaline earth metal salts are mixed with No. 3 water glass, J-roids are rapidly formed in the mixed solution.
There is a problem in that the gelation time varies greatly depending on the elapsed time until the liquid is added, making it difficult to adjust the gelation time.
また、水ガラスに強酸を加えて形成される酸性水ガラス
を基本素材とし2、これにrルカリ剤を加える注入工法
も知られζ゛いるが、この場合、強酸を用いるこきによ
る現場1〔、おf、lる取り扱い土の問題や、ゲル化時
間が調整し2にくいという欠点を有し2ている。In addition, there is also known an injection method in which acidic water glass, which is formed by adding a strong acid to water glass, is used as the basic material2, and an rlkali agent is added to it. However, it has disadvantages such as the problem of handling soil and the difficulty in adjusting the gelling time.
〔発明が解決し2ようと引る問題点J
水ガラスと反応剤をあらかじ綽混合jバーなイ、イれ自
体ゲル化し得る配合液を基本素材と11、これにゲル化
剤を加えて゛なるツノ法は、基本素オΔが必ずゲル化す
るため、これ1.“ゲル化剤苓加オ′コゲル化時間を調
整し1.た注入液も必ずゲル化し1、地盤中1ごおける
固結性が極めC゛優れこいる2−いう長所がある。[Problems that the invention attempts to solve 2. Water glass and reactant are mixed together. First, a mixture that can gel itself is used as the basic material 11, and a gelling agent is added to it.] In the horn method, the basic element O Δ always gels, so 1. It has the following advantages: 1) The gelling agent and the gelation time are adjusted; 1) the injection solution is always gelatinized; and 2) the solidification property in the ground is extremely good.
し、かし1、この方法の最大の欠点は基本素材4配合後
、ぞの内部びjロイドの生成が急速j、進行腰その生成
は配合後から注入に至、るiひの時間の経過につれC加
速される。しまたか−、で、この基本素材(A液)にゲ
ル化剤(B液)を加えてゲル化時間を調整しようとして
も、A、B混合液のゲル化時間は基本3I材(A液)の
配合時からA液にB液を混合するまでの経過時間によっ
てゲル化時間が異なり、所定のゲル化時間を得ることが
極y〕で難しい。However, 1. The biggest drawback of this method is that after mixing the basic materials, the formation of intracranial roids is rapid and progresses. C is accelerated as the speed increases. Also, even if you try to adjust the gelling time by adding a gelling agent (liquid B) to this basic material (liquid A), the gelling time of the mixed liquids A and B will be the same as the basic 3I material (liquid A). The gelation time varies depending on the elapsed time from the time of blending until the time when the B solution is mixed with the A solution, and it is extremely difficult to obtain a predetermined gelation time.
実際の現場では、基本素材であるA液を作液[2でから
ASB液を混合して注入に至るにでに種々の作業、たと
えば注入]枠中の注入ステージの変化による注入の中止
、注入管の詰まりによる水洗い、その他のトラブル等に
よる注入の一時中断、昼休みの注入の中断、ポンプの調
整等が生じ、あるいはその他、B液そのものの配合の調
整、個々の注入管に至るまでの距離の違い等によりA液
にB液を混合して注入する状態になるまでに多かれ少な
かれ、時間を要し、その時間も一定のものではない。し
たがって、もし、A液を配合後B液を加えるまでの経過
時間の長短にもかかわらず、ゲル化時間が変化しにくい
方法を見い出せれば、この注入方式はゲル化時間の設定
が容易な工法として極めて優れた、実用性の高い工法に
なり得るはずである。In the actual field, the basic material, A liquid, is prepared [from step 2, ASB liquid is mixed and various operations are performed before injection, such as injection], and injections may be stopped or injected due to changes in the injection stage within the frame. Flushing due to a clogged pipe, temporary suspension of injection due to other problems, suspension of injection during lunch break, adjustment of the pump, etc., or adjustments to the composition of liquid B itself, or changes in the distance to each injection tube. Due to differences, etc., it takes more or less time to mix and inject liquid A and liquid B, and the time is not constant. Therefore, if we can find a method in which the gelation time is less likely to change regardless of the length of time that elapses between blending Part A and adding Part B, this injection method would be a method that would allow easy setting of the gelation time. This should be an excellent and highly practical construction method.
また、施工が大規模になると、−時に大量の注入素材を
つくり、それから多数のポンプを用いて多数の注入管に
送液し、それぞれにゲル化剤を加えてゲル化時間を調整
し、注入することになるが、−時につくられる注入素材
量が多いほど注入が始まってからその注入素材が使い尽
くされるまでiコ時間がかかるから、その間の時間の経
過にもかかわらず、ゲル化時間の変鮎が少なければ大量
施]、に適し7た注入工法が可能になる。In addition, when construction becomes large-scale, a large amount of injection material is sometimes made, and then multiple pumps are used to send the liquid to many injection pipes, a gelling agent is added to each, the gelation time is adjusted, and the injection material is injected. However, the larger the amount of injection material produced at a time, the longer it takes from the start of injection until the injection material is used up, so regardless of the elapsed time, the gelation time If there are only a few hen-ayu, it becomes possible to use a more suitable injection method for large-scale treatment.
そこで、本発明の目的はゲル化時間の調整が容易で、か
つ浸透性に優れ、前述の公知技術に存する欠点を改良し
た地盤注入工法を提供することにある。SUMMARY OF THE INVENTION Therefore, an object of the present invention is to provide a ground injection method that allows easy adjustment of gelation time, has excellent permeability, and improves the drawbacks of the above-mentioned known techniques.
〔問題点を解決するための手段J
前述の目的を達成するため、本発明によれば、以下の(
A)または(B)のいずれかの条件を満たす配合液を基
本素材とし、この基本素材に反応剤を添加し2てゲル化
時間を調整してなるTルカリ性注入液を地盤中に注入す
ることを特wi、= する。[Means for Solving the Problems J In order to achieve the above-mentioned object, according to the present invention, the following (
A compounded liquid that satisfies either of the conditions of A) or (B) is used as the basic material, a reactant is added to this basic material, and the gelation time is adjusted to inject the T-rucaritic injection into the ground. Specially = do something.
0モル比が2.8JJ下の水ガラスとI″iJ溶性反応
剤とを有効成分とイるゲル化時間が1時間よりも長いア
ルカリ性を呈する配合液。A compounded solution exhibiting alkalinity and having a gelation time longer than 1 hour, the active ingredients being water glass with a zero molar ratio of 2.8 JJ or less and an I''iJ soluble reactant.
■水ガラスと水溶性アルカリと1liJ溶性反応剤を有
効成分とするゲル化時間が1時間よりも長いアルカリ性
を〒する配合液。■An alkaline compound containing water glass, a water-soluble alkali, and a 1liJ-soluble reactant as active ingredients with a gelation time of more than 1 hour.
上述の本発明における水ガラスとし7では、前述の(A
)ではモル比が2,8以ト、好ましくは245〜0゜5
であって、液状または粉状のものであり、また、前述の
(B)では5iOz/Me2O(モル比)が2□8以上
、好まシ、<は288〜0,5である。ここで、510
2は水ガラスに基因するシリカ分を表し、Me2Oは水
ガラスと水溶性°アルカリに基因寸“るアルカリ分を表
す。In the above-mentioned water glass 7 according to the present invention, the above-mentioned (A
), the molar ratio is 2.8 or more, preferably 245 to 0.5
In the above-mentioned (B), 5iOz/Me2O (molar ratio) is preferably 2□8 or more, preferably 288 to 0.5. Here, 510
2 represents the silica content based on water glass, and Me2O represents the alkali content based on water glass and water-soluble alkali.
さらに、前述(A>および(B)における可溶性反応剤
としでは、可溶性無機塩、例えばNa。Furthermore, as the soluble reactant in the above (A> and (B)), a soluble inorganic salt, such as Na.
K等の一価金属塩化物、硫酸塩、リン酸塩、重炭酸塩、
(’: aCl 2、MgCl2等のアルカリ土金属塩
化物、アルミン酸ソーダ、アルミン酸リチウム等のアル
ミン酸塩、A1.2Cl3、ポリ塩化アルミニウム、硫
酸アルミニウム、酸化アルミニウム、みょうばん等の近
値金属塩、FeC1,i、FezSO+。Monovalent metal chlorides, sulfates, phosphates, bicarbonates, such as K,
(': Alkaline earth metal chlorides such as aCl2, MgCl2, aluminates such as sodium aluminate, lithium aluminate, near-value metal salts such as A1.2Cl3, polyaluminum chloride, aluminum sulfate, aluminum oxide, alum, etc. FeC1,i, FezSO+.
等の鉄塩が用いられるが、その他任意の無機、酸、1機
酸、アルデしド、エステル等も同様に使用司能である。Iron salts such as, etc. are used, but any other inorganic, acid, monoacid, aldehyde, ester, etc. can be used as well.
また、前記(B)1こおける水溶性rルカリ2・し。In addition, the water-soluble r-lukali 2 in the above (B) 1.
では苛性rルカリ等が用いられる。In this case, caustic rukali etc. are used.
さら1い前記基本素4Aに添加される反応剤と1゜ては
、無機塩、無機酸、イ】機反応剤、セメント、スラグ、
6灰(消右灰、炭酸カルシウム、炭酸マグネシウム等)
等、任意のものが用いられる。Furthermore, the reactants added to the basic element 4A include inorganic salts, inorganic acids, organic reactants, cement, slag,
6 ash (slaked ash, calcium carbonate, magnesium carbonate, etc.)
etc., any one can be used.
上述の基本素材はゲル化時間が1時間以1.吃有し、か
つアルカリ性であ−、で、この基本素材1.二反応剤を
加λてなる汀入液もま−た、アルカリ性4早するもので
ある。The basic materials mentioned above have a gelling time of 1 hour or more. This basic material 1. is stinky and alkaline. The inlet solution with the addition of two reactants also becomes alkaline.
以下、本発明を実験に、111.で詳述する1、Δ液お
よび■3液を表−1乃至(〕に小4゛よ・“)に調整す
る。Hereinafter, the present invention will be used as an experiment in 111. Adjust the solutions 1, Δ and 3 described in Table-1 to () to a small amount of 4".
表−1
表−3
表−2
表−4
表−5
実験−1
表−1乃至4に示されるA液を配合の後、これに表−5
のB液を混合するまでの時間に対応してゲル化時間(2
0℃)を測定した。A、B液を同量づつ合流混合した急
結配合の経過時間(時間)に対するゲル化時間(秒)の
試験結果(20℃)を第1図に示す。Table-1 Table-3 Table-2 Table-4 Table-5 Table-5 Experiment-1 After blending liquid A shown in Tables-1 to 4, Table-5
The gelation time (2
0°C) was measured. FIG. 1 shows the test results (at 20° C.) of gelation time (seconds) versus elapsed time (hours) for a rapid setting formulation in which equal amounts of liquids A and B were mixed together.
A、B液の組み合わせは第1図中、■は、’l−にB−
2、■はΔ−2:B−2、■はA、−4:84、■は八
−5:B−3、■はA、−3:B−4■はA−7:B−
5、■はA−8:B−2、■はA−9:B−4、■はA
−11:B−5、■はA10:B−1、■はA、−18
:B−1コ■はA−19:B−1、■はA−228B−
5、■はA−27:B3である。The combination of A and B liquids is shown in Figure 1.
2, ■ is Δ-2:B-2, ■ is A, -4:84, ■ is 8-5:B-3, ■ is A, -3:B-4 ■ is A-7:B-
5,■ is A-8:B-2, ■ is A-9:B-4, ■ is A
-11:B-5, ■ is A10:B-1, ■ is A, -18
: B-1 ■ is A-19:B-1, ■ is A-228B-
5, ■ is A-27:B3.
第1図より、A液として3号水ガラスを用いた場合には
経過時間とともにゲル化時間が大幅に変動することがわ
かる。From FIG. 1, it can be seen that when No. 3 water glass is used as liquid A, the gelation time varies significantly with elapsed time.
それに対して本発明ではA液配合の後長時間を経てもゲ
ル化時間の変動が極めて少ない領域があることがわかる
。ただし、A液のゲル化時間が60分よりも短い場合は
ゲル化時間は比較的短縮しやすくなることがわかる。こ
れより基本素材のゲル化時間は60分よりも長い方が望
ましいことがわかる。On the other hand, in the present invention, it can be seen that there is a region in which the gelation time fluctuates very little even after a long period of time has passed after the addition of liquid A. However, it can be seen that when the gelation time of liquid A is shorter than 60 minutes, the gelation time can be relatively easily shortened. From this, it can be seen that it is desirable that the gelation time of the basic material be longer than 60 minutes.
すなわち、3号水ガラスの場合には、基本素材の内部で
配合直後からコロイドの形成が急に行なわれるのに対し
、モル比が低い場合にはコロイドの形成が遅れるためと
思われる。ただし、ゲル化時間が1時間以内の配合では
ゲル化が早い時期に進行するものと思われる。That is, in the case of No. 3 water glass, colloid formation occurs rapidly within the basic material immediately after blending, whereas when the molar ratio is low, colloid formation is delayed. However, if the gelation time is less than 1 hour, the gelation will likely proceed quickly.
表−6にアルカリ材を加えた基本素材を例示する。アル
カリ材としては単独では水ガラスにゲル化を生じさせな
いアルカリまたはアルカリ性塩であって、具体的には苛
性アルカリ、炭酸ソーダ等が挙げられ、特に苛性アルカ
リが好ましい。A#。Table 6 shows examples of basic materials to which alkaline materials are added. The alkaline material is an alkali or an alkaline salt that does not cause gelation in water glass when used alone, and specific examples thereof include caustic alkali and soda carbonate, with caustic alkali being particularly preferred. A#.
の作液に当たっては水ガラス水溶液と反応剤水溶液を混
合するが、苛性アルカリはあらかじめいずれかに混入し
ておいてもよい。In preparing the solution, the water glass aqueous solution and the reactant aqueous solution are mixed, but caustic alkali may be mixed in either of them in advance.
表−6から、アルカリを用いでも基本素材のゲル化の急
激な進行がおさえられ、これに反応剤4加えた場合、一
定なゲル化時間を呈する広範囲な領域が存在することが
わかる。From Table 6, it can be seen that even when alkali is used, the rapid progress of gelation of the basic material is suppressed, and when reactant 4 is added to this, there is a wide range where the gelation time is constant.
実験−2
細砂への注入試験
内径5cm、高さ50cmのモールド中に細砂(1)、
。Experiment-2 Injection test into fine sand Fine sand (1) was placed in a mold with an inner diameter of 5 cm and a height of 50 cm.
.
0、07mm5D Io: 0.05mm、 D 、、
: 0412闘、[)9゜0、151T1m)を填充
して、小型注入ポンプを用いてモールド下面から第1図
の代表的な配合液を注入し1、注入時の浸透状況を観察
するとともに、24時間後に最下端ならびに最上端10
cm長の固結体を取り出し、これらの−軸圧縮強度を測
定した。結果を表−7に示す。基本素材に対する反応剤
の配合は基本素材を保液後、1時間経てから行なった。0.07mm5D Io: 0.05mm, D,,
: 0412T, [)9゜0, 151T1m) was filled, and a typical compounded solution shown in Figure 1 was injected from the underside of the mold using a small injection pump.1, while observing the permeation situation at the time of injection, After 24 hours, the bottom and top 10
The cm-long solid bodies were taken out and their -axial compressive strengths were measured. The results are shown in Table-7. The reactant was added to the base material one hour after the base material was retained in the liquid.
表−7に示されるように、浸透状況は表−7に示される
ように1乃至■グループに分類される。。As shown in Table-7, the penetration status is classified into groups 1 to 2, as shown in Table-7. .
なお、第1図におりる実施に6〜9および11〜14に
ついては実験は行なわないが、第1グループに属するも
のである。Incidentally, although experiments were not conducted for items 6 to 9 and 11 to 14 in the implementation shown in FIG. 1, they belong to the first group.
表−7から、A液として3号水ガラスを用いた場合には
、配合初期段階で珪酸コロイドの凝集が進行し、これが
細砂に対して浸透を阻害し、かっ固結を不均質にし、さ
らに強度も低下し、全体を均質に固結できないことがわ
かる。From Table 7, when No. 3 water glass is used as liquid A, coagulation of silicic acid colloid progresses in the initial stage of blending, which inhibits penetration into fine sand and makes the coagulation non-uniform. Furthermore, the strength decreased, and it was found that the whole could not be consolidated homogeneously.
これに対して、本発明によれば、コロイドの形成が防止
され、最終的には均質なゲル化をもたらし、大きな強度
を得ることがわかる。In contrast, it can be seen that according to the present invention, the formation of colloids is prevented, ultimately leading to homogeneous gelation and high strength.
また、A液のゲル化時間は1時間以上が浸透の点から好
ましいことがわかる。Further, it can be seen that it is preferable for the gelation time of liquid A to be 1 hour or more from the viewpoint of penetration.
以上の本発明の特性を利用して実際の注入に当たっては
、すべての注入方式に用いることができ、特に、A液に
瞬結用B液を合流して瞬結グラウトを注入する工程と、
A液に緩結用B液等合流し2て緩結グラウトを注入する
工程と4組み合わセ注入することにより極めて効果的に
地盤固結症達成できる。In actual injection using the above characteristics of the present invention, it can be used for all injection methods, especially the step of combining liquid A with liquid B for instant setting and injecting instant setting grout,
Ground consolidation can be extremely effectively achieved by combining the steps of merging liquid A with liquid B for loosening, and then injecting loosely setting grout.
さらに基本素材の保液に当てては水ガラス♂−可溶性反
応剤、ないしはさらに水溶性アルカリとを任意に混合す
ることもでき、たとえば、これらの加圧噴射合流混合方
式により急結混合すれば部分ゲルを生じることがない。Furthermore, for liquid retention of the basic material, water glass ♂ - soluble reactant, or even water-soluble alkali can be optionally mixed. No gel formation occurs.
上述のとおり、本発明はそれ自体ゲル化し得る、水ガラ
スと可溶性反応剤ないしはさらに水溶性アルカリと混合
液を基本素材とし、これに反応剤を加えて得られた注入
液を地盤中に注入することを特徴とし、これによって従
来の注入方式に存する欠点を解決したものであって、基
本素材を保液したのち、長時間にわたって任意に反応剤
を加えてもゲル化の変動が少なく、浸透性にもすぐれて
、作業性にすぐれ、所定のゲル化時間をうろことができ
、しかも確実にゲル化するため注入効果もすぐれ、極め
て実用性のある発明である。As mentioned above, the present invention uses a mixture of water glass and a soluble reactant or a water-soluble alkali as a basic material, which can itself be gelatinized, and adds the reactant to the mixture, and injects the obtained injection liquid into the ground. This method solves the drawbacks of conventional injection methods; after retaining the basic material, even if a reactant is optionally added over a long period of time, there is little change in gelation, and the permeability is improved. It is an extremely practical invention, as it has excellent workability, allows for a predetermined gelation time, and also has excellent injection effects because it gels reliably.
第1図はA液の経過時間とΔ、3合流液のゲル化時間の
関係を表i、、、、 フ:グラフである。FIG. 1 is a graph showing the relationship between the elapsed time of solution A and the gelation time of Δ and 3 combined solutions.
Claims (1)
たす配合液を基本素材とし、この基本素材に反応剤を添
加してゲル化時間を調整してなるアルカリ性注入液を地
盤中に注入することを特徴とする地盤注入工法。 [1]モル比が2.8以下の水ガラスと可溶性反応剤と
を有効成分とするゲル化時間が1時間よりも長いアルカ
リ性を呈する配合液。 [2]水ガラスと水溶性アルカリと可溶性反応剤を有効
成分とするゲル化時間が1時間よりも長いアルカリ性を
呈する配合液。(1) The basic material is a compounded liquid that satisfies either of the following conditions (A) or (B), and an alkaline injection liquid is poured into the ground by adding a reactant to this basic material and adjusting the gelation time. A ground injection method characterized by injecting water into the ground. [1] An alkaline compound containing water glass and a soluble reactant with a molar ratio of 2.8 or less as active ingredients and having a gelation time longer than 1 hour. [2] A liquid mixture containing water glass, a water-soluble alkali, and a soluble reactant as active ingredients and exhibiting alkalinity with a gelation time longer than 1 hour.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2208046A JP2554953B2 (en) | 1990-08-08 | 1990-08-08 | Ground injection method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2208046A JP2554953B2 (en) | 1990-08-08 | 1990-08-08 | Ground injection method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0492013A true JPH0492013A (en) | 1992-03-25 |
| JP2554953B2 JP2554953B2 (en) | 1996-11-20 |
Family
ID=16549749
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2208046A Expired - Fee Related JP2554953B2 (en) | 1990-08-08 | 1990-08-08 | Ground injection method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2554953B2 (en) |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01190786A (en) * | 1988-01-27 | 1989-07-31 | Kyokado Eng Co Ltd | Material for solidification |
| JPH01192912A (en) * | 1988-01-27 | 1989-08-03 | Shimoda Gijutsu Kenkyusho:Kk | Grouting work using sea water |
| JPH0489912A (en) * | 1990-07-31 | 1992-03-24 | Kyokado Eng Co Ltd | Grouting construction method |
-
1990
- 1990-08-08 JP JP2208046A patent/JP2554953B2/en not_active Expired - Fee Related
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01190786A (en) * | 1988-01-27 | 1989-07-31 | Kyokado Eng Co Ltd | Material for solidification |
| JPH01192912A (en) * | 1988-01-27 | 1989-08-03 | Shimoda Gijutsu Kenkyusho:Kk | Grouting work using sea water |
| JPH0489912A (en) * | 1990-07-31 | 1992-03-24 | Kyokado Eng Co Ltd | Grouting construction method |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2554953B2 (en) | 1996-11-20 |
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