JPH0362749B2 - - Google Patents
Info
- Publication number
- JPH0362749B2 JPH0362749B2 JP57014038A JP1403882A JPH0362749B2 JP H0362749 B2 JPH0362749 B2 JP H0362749B2 JP 57014038 A JP57014038 A JP 57014038A JP 1403882 A JP1403882 A JP 1403882A JP H0362749 B2 JPH0362749 B2 JP H0362749B2
- Authority
- JP
- Japan
- Prior art keywords
- soil
- acid
- salt
- solution
- cement
- 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
Landscapes
- Soil Conditioners And Soil-Stabilizing Materials (AREA)
- Consolidation Of Soil By Introduction Of Solidifying Substances Into Soil (AREA)
Description
本発明は、珪酸塩水溶液とセメント懸濁液とを
混合して得られたグラウト剤を土壌に注入してゲ
ル化させ、土壌粒子を固化することによつて土質
を強化し、液体不浸透性となして土質を安定化す
る工法に関するものである。
従来より珪酸塩を用いたグラウト剤により土質
の安定化を行うことはよく知られている。珪酸塩
系のグラウト剤としては、珪酸塩−セメント系の
懸濁型或いは珪酸塩−水溶性硬化剤系の溶液型の
ものが知られている。前記懸濁型についてはゲル
化時間の調整がむづかしく、特に、短時間でゲル
化させることが困難であるという欠点を有し、
又、溶液型に比して廉価な割には土質安定効果が
高いという長所を有するが、近年、グラウト剤自
身のゲル強度及び安定化処理された土壌の強度を
より一層高めることが要望されている。しかして
グラウト剤のゲル化時間の短縮を目的として硬化
剤であるセメント懸濁液にアルミン酸のアルカリ
金属塩を添加することが知られているが、この場
合はセメント懸濁液の安定性が悪くなり貯蔵又は
輸送中に該懸濁液がゲル化し易いという欠点があ
つた。
本発明は上記従来の土質の安定化処理工法の現
状に鑑み、貯蔵安定性の良好なセメント懸濁液を
用いてゲル化時間を容易に広範に調整出来、又作
業性良く土質の安定化処理を行うことが出来、さ
らにゲル強度及び固結土強度も従来法に比して同
等以上のものが得られる土質の安定化処理工法を
提供することを目的としてなされたものである。
しかして本発明の要旨は、
A液:珪酸のアルカリ金属塩水溶液
B液:高炉コロイドセメント、アルミン酸のアル
カリ金属塩、水およびキレート化剤が含有され
てなり、水対セメントの重量比が1〜6である
水懸濁液
上記A、B両液を混合して得られた水性混合液
を土壌に注入することを特徴とする土質の安定化
処理工法に存する。
A液における珪酸のアルカリ金属塩としては珪
酸ナトリウム、珪酸カリウム等が挙げられ、珪酸
ナトリウム(別名水ガラス)が特に好適であり、
水溶液としてJIS K 1408に規格されている1
号、2号、3号の珪酸ナトリウムが常用されてい
る。その使用量は注入する土壌の状態や目的に応
じて適宜決定されるが、例えば上記JISにもとづ
く1号〜3号の珪酸ナトリウムを用いる場合は、
上記水性混合液に対して5〜50容量%、好ましく
は10〜40容量%とされる。
B液に用いられる高炉コロイドセメントは、一
般セメントとは成分が異なり、海水に強くまた微
粒子であるために浸透性も良好であるという特徴
を有するものである。高炉コロイドセメントの使
用量は、通常、セメント懸濁液における水対セメ
ントの重量比(以下W/Cと略記する)で表わさ
れ、本発明においてはB液におけるW/Cが1〜
6とされる。高炉コロイドセメント量が多い程固
結土強度や注入液自身のゲル化物の強度が強くな
る傾向にあるが、W/Cが小さ過ぎると水濁液の
流動性が悪くなり、大き過ぎると注入液のゲル強
度や固結土強度が低下することとなる。
B液に用いられるアルミン酸のアルカリ金属塩
としてはアルミン酸のカリウム塩、ナトリウム
塩、リチウム塩等が挙げられ、特にアルミン酸ナ
トリウムが多用される。これらのアルミン酸塩は
単独で又は適宜混合して用いられ、使用量が少な
過ぎると水性混合液のゲル化物の強度や固結土強
度が低くなり、多過ぎても特に相応の効果が生じ
ないので、通常は酸化アルミニウム(AI2O3)の
含有量が上記水性混合液に対して0.3〜25重量%、
好ましくは0.5〜18重量%となる範囲で用いられ
る。
B液に用いられるキレート化剤は、高炉コロイ
ドセメントが水中に懸濁されて生ずる金属イオン
と結合してキレート化合物を形成し得る無機物、
有機物が広く用いられ、有機物の具体例として
は、シユウ酸、マロン酸、コハク酸、マレイン
酸、イタコン酸等の多塩基酸、乳酸、βオキシ
酸、グリセリン酸、グルコン酸、リンゴ酸、酒石
酸、クエン酸、サリチル酸等のオキシ酸、そのナ
トリウム酸及びカリウム塩、エチレンジアミン、
ジエチレントリアミン、N,N−ジ−エチレンジ
アミン、エチレンジアミンテトラ酢酸等の脂肪族
アミン、α,α′−ジピリジル等の芳香族アミン、
アラニン、アスパラギン、アスパラギン酸、グル
シン、グルタミン酸、セリン等のアミノ酸、ニト
ロ酢酸等のニトロカルボン酸が挙げられ、無機物
の具体例としてはピロリン酸、テトラメタリン
酸、トリメタリン酸、トリリン酸等の縮合リン
酸、そのナトリウム塩及びカリウム塩が挙げられ
る。これらのキレート化剤の内、取り扱い易さ、
キレート化合物の生成し易さ経済性等の点からオ
キシ酸及び二塩基酸が常用され特に酒石酸、クエ
ン酸、これらのナトリウム塩及びカリウム塩が好
ましく用いられる。
本発明においては、B液に用いられる高炉コロ
イドセメントが水中に懸濁されて生ずる金属イオ
ンの一部がキレート化剤と結合することによつ
て、該金属イオンとアルミン酸のアルカリ金属塩
との反応を阻害もしくは遅延させ結果的にB液を
安定化するものと推定される。
又、その理由は不明であるが、アルミン酸塩及
びキレート化剤が添加されていない従来の懸濁型
土質安定剤と同量の上記水性混合液を用いると、
従来より多量の土壌が固結され且つ固結土の強度
が高いという知見が得られた。
上記キレート化剤の使用量は、少な過ぎるとB
液の安定性が悪くなり多過ぎると凝固物が生成さ
れるので、一般に上記水性混合液に対して0.03〜
1.5重量%、好ましくは0.05〜1.2重量%とされる。
例えば水とセメントのみからなる、アルミン酸
のアルカリ金属塩を含有しない硬化剤を用いる従
来の懸濁型グラウト剤においては、珪酸塩水溶液
とセメント懸濁液とを混合してからゲル化する迄
の時間は早い場合でも2分間程度要していたが、
本発明において必要な場合は、B液組成及びA,
B両液の混合比を適宜調整することにより前記ゲ
ル化時間を数秒間にすることも可能である。
次に本発明により土質を安定化するには、上記
A液及びB液を混合して得られた水性混合液を土
壌中に注入するのである。土壌中に水性混合液を
注入するには、通常、注入用のポンプを用いて土
壌中に挿入されたパイプを通じて圧入することに
より行われる。そして本発明においては、別々に
用意したA、B両液を一定量ずつ同時に注入パイ
プに送り、そこで該両液を合流させ混合する様に
するのが好ましい。本発明におけるB液は常温下
で通常数時間はゲル化しないのでA液と混合され
ない内にパイプ中で固結することはない。無論、
場合によつてはA液B液を配合タンク内に投入し
て撹拌混合したのちにパイプに送給する方法も可
能である。かくして土壌中に注入された混合液
は、その中に含まれる高炉コロイドセメント、ア
ルミン酸のアルカリ金属塩等の量により予め設定
されたゲル化時間に達すれば含水ゲルとなり、該
混合物が注入された範囲の土粒子を固定化し、該
土壌に高い一軸圧縮強度を付与すると共に、液体
不浸透性を付与して土質の安定化が行われるので
ある。
本発明の土質の安定化処理工法は上述の通りの
構成になされており、上記A液と貯蔵安定性の良
いB液とを混合して得られた水性混合液を土壌に
注入することを特徴とするものであるから、B液
を調整後A液と直ちに混合する必要がなくB液が
注入パイプ中でゲル化することがない点や水性混
合液のゲル化時間を短時間から長時間迄容易に広
範に調整出来る点、及びW/Cが特定されている
のでB液ひいては水性混合液の流動性が良好な点
で作業性が良好であり、又、本発明によればアル
ミン酸のアルカリ金属塩を含まない従来の懸濁型
グラウト剤を用いた工法に比して多量の土壌を固
結させることが可能で且つ一軸圧縮強度の高い固
結土が得られ、更に層境注入や割裂注入の場合等
に要請される高い強度を有する注入液のゲル化物
が得られるのである。
特に、本発明に用いられる高炉コロイドセメン
トは一般セメントに比較すると微粒子であるため
浸透性が大きく、より広い範囲にわたつて土粒子
を固定化出来る利点を有し、更には海水に対する
耐性の高いゲル化物を与えることが出来るため、
海水の混入が想定されるような土質の安定化にも
適したものとなる。
以下に本発明の実施例を示す。単に部又は%と
あるのは重量部又は重量%を表わすものとする。
実施例 1〜4
JIS K 1408にもとづく1号珪酸ソーダ112部
及び水25部よりなるA液と第1表に示された組成
のアルミン酸ソーダ(粉末、Al2O3分37%含有)、
キレート化剤及び高炉コロイドセメントに水を加
えて作成したB液とを用意した。20℃におけるこ
のB液の安定性と、A液及びB液を容積比で1:
1の割合で混合したときのゲルルタイムと硬化物
を湿砂中で7日間養生をしたときの一軸圧縮強度
の測定値は第1表に示される通りであつた。
The present invention aims to inject a grouting agent obtained by mixing a silicate aqueous solution and a cement suspension into soil and gel it, thereby solidifying soil particles to strengthen the soil and make it impermeable to liquids. This relates to construction methods that stabilize soil quality. It has been well known that soil quality can be stabilized by grouting agents using silicate. As silicate-based grouting agents, silicate-cement-based suspension types and silicate-water-soluble hardener-based solution types are known. Regarding the suspension type, it is difficult to adjust the gelation time, and in particular, it is difficult to gel in a short time.
In addition, it has the advantage of being less expensive and highly effective in stabilizing the soil compared to solution-type grouting agents, but in recent years, there has been a demand to further increase the gel strength of the grout itself and the strength of the stabilized soil. There is. However, it is known that an alkali metal salt of aluminate is added to a cement suspension as a hardening agent in order to shorten the gelation time of the grout, but in this case, the stability of the cement suspension may be affected. There was a drawback that the suspension tended to gel during storage or transportation. In view of the current state of the conventional soil stabilization treatment methods mentioned above, the present invention provides soil stabilization treatment that allows gelation time to be easily adjusted over a wide range by using a cement suspension with good storage stability, and has good workability. The purpose of this invention is to provide a soil stabilization method that can achieve gel strength and compacted soil strength equivalent to or better than conventional methods. Therefore, the gist of the present invention is as follows: Solution A: aqueous solution of alkali metal salt of silicic acid Solution B: contains blast furnace colloidal cement, alkali metal salt of aluminate, water, and a chelating agent, and the weight ratio of water to cement is 1. - 6 Aqueous Suspension A soil stabilization treatment method characterized by injecting into soil an aqueous mixed solution obtained by mixing both solutions A and B above. Examples of the alkali metal salt of silicic acid in liquid A include sodium silicate, potassium silicate, etc., and sodium silicate (also known as water glass) is particularly suitable.
Standardized in JIS K 1408 as an aqueous solution 1
Sodium silicate No. 2, No. 3 is commonly used. The amount to be used is determined appropriately depending on the condition of the soil to be injected and the purpose. For example, when using sodium silicate No. 1 to No. 3 based on the above JIS,
The amount is 5 to 50% by volume, preferably 10 to 40% by volume, based on the aqueous mixture. The blast furnace colloidal cement used for liquid B has different components from general cement, and has the characteristics of being resistant to seawater and having good permeability due to its fine particle size. The amount of blast furnace colloidal cement used is usually expressed as the weight ratio of water to cement in the cement suspension (hereinafter abbreviated as W/C), and in the present invention, W/C in liquid B is 1 to 1.
6. The larger the amount of blast furnace colloidal cement, the stronger the solidified soil strength and the strength of the gelled material of the injected liquid itself. However, if the W/C is too small, the fluidity of the water suspension will deteriorate, and if it is too large, the injected liquid will become stronger. The gel strength and compacted soil strength will decrease. Examples of the alkali metal salt of aluminate used in the B solution include potassium salt, sodium salt, lithium salt, etc. of aluminate, and sodium aluminate is particularly frequently used. These aluminates are used alone or in an appropriate mixture; if the amount used is too small, the strength of the gelled product of the aqueous mixture and the strength of the compacted soil will be low, and if the amount is too large, no particular effect will be produced. Therefore, the content of aluminum oxide (AI 2 O 3 ) is usually 0.3 to 25% by weight based on the above aqueous mixture.
It is preferably used in a range of 0.5 to 18% by weight. The chelating agent used in Solution B is an inorganic substance that can combine with metal ions generated when blast furnace colloidal cement is suspended in water to form a chelate compound.
Organic substances are widely used, and specific examples of organic substances include polybasic acids such as oxalic acid, malonic acid, succinic acid, maleic acid, and itaconic acid, lactic acid, β-oxyacid, glyceric acid, gluconic acid, malic acid, tartaric acid, Oxyacids such as citric acid and salicylic acid, their sodium acids and potassium salts, ethylenediamine,
Aliphatic amines such as diethylenetriamine, N,N-di-ethylenediamine, ethylenediaminetetraacetic acid, aromatic amines such as α,α′-dipyridyl,
Examples of inorganic substances include amino acids such as alanine, asparagine, aspartic acid, glucine, glutamic acid, and serine, and nitrocarboxylic acids such as nitroacetic acid. Specific examples of inorganic substances include condensed phosphoric acids such as pyrophosphoric acid, tetrametaphosphoric acid, trimetaphosphoric acid, and triphosphoric acid. , its sodium and potassium salts. Among these chelating agents, ease of handling,
Oxyacids and dibasic acids are commonly used from the viewpoint of ease and economy in producing chelate compounds, and tartaric acid, citric acid, and their sodium and potassium salts are particularly preferred. In the present invention, a part of the metal ions generated when the blast furnace colloidal cement used in the B liquid is suspended in water combine with the chelating agent, thereby forming a bond between the metal ions and the alkali metal salt of aluminate. It is presumed that the reaction is inhibited or delayed and as a result, the B solution is stabilized. Also, although the reason is unknown, when using the same amount of the above aqueous mixture as a conventional suspended soil stabilizer to which no aluminate or chelating agent is added,
It was found that a larger amount of soil was consolidated than before, and that the strength of the consolidated soil was higher. If the amount of the above chelating agent used is too small, B
Since the stability of the liquid deteriorates and coagulates are formed if the amount is too high, generally 0.03~
The amount is 1.5% by weight, preferably 0.05-1.2% by weight. For example, in a conventional suspension grouting agent that uses a curing agent that does not contain an alkali metal salt of aluminate, which is made only of water and cement, a silicate aqueous solution and a cement suspension are mixed and then gelled. Even if it was quick, it would take about 2 minutes,
If necessary in the present invention, the composition of B liquid and A,
By appropriately adjusting the mixing ratio of both liquids B, it is possible to make the gelation time several seconds. Next, in order to stabilize soil quality according to the present invention, an aqueous liquid mixture obtained by mixing the above-mentioned liquids A and B is injected into the soil. Injecting the aqueous mixture into the soil is usually carried out by using an injection pump to force the mixture through a pipe inserted into the soil. In the present invention, it is preferable that a fixed amount of both liquids A and B, which are prepared separately, are simultaneously sent to the injection pipe, where the two liquids are brought together and mixed. In the present invention, the B liquid does not usually gel for several hours at room temperature, so it does not solidify in the pipe before being mixed with the A liquid. Of course,
In some cases, it is also possible to introduce the A and B solutions into a mixing tank, stir and mix them, and then feed them to the pipe. The mixture thus injected into the soil becomes a hydrogel when it reaches a preset gelation time depending on the amount of blast furnace colloidal cement, alkali metal salt of aluminate, etc. contained therein, and the mixture is injected into the soil. This stabilizes the soil quality by immobilizing soil particles within a range, imparting high unconfined compressive strength to the soil, and imparting liquid impermeability to the soil. The soil stabilization treatment method of the present invention is configured as described above, and is characterized by injecting into the soil an aqueous liquid mixture obtained by mixing the above-mentioned liquid A and liquid B, which has good storage stability. Therefore, there is no need to mix the B solution with the A solution immediately after adjustment, the B solution does not gel in the injection pipe, and the gelation time of the aqueous mixture can be extended from a short time to a long time. Workability is good in that it can be easily adjusted over a wide range, and since the W/C is specified, the fluidity of the B solution and even the aqueous mixed solution is good, and according to the present invention, the alkali of aluminate Compared to construction methods using conventional suspension grouting agents that do not contain metal salts, it is possible to consolidate a large amount of soil and obtain consolidated soil with high unconfined compressive strength. This makes it possible to obtain a gelled product of the injection liquid that has the high strength required for injections and the like. In particular, since the blast furnace colloidal cement used in the present invention has fine particles compared to general cement, it has greater permeability and has the advantage of being able to immobilize soil particles over a wider area, and is also a gel that has high resistance to seawater. Because it can give monsters,
It is also suitable for stabilizing soil quality where seawater contamination is expected. Examples of the present invention are shown below. The term "parts" or "%" refers to parts by weight or percentages by weight. Examples 1 to 4 Solution A consisting of 112 parts of No. 1 sodium silicate based on JIS K 1408 and 25 parts of water, and sodium aluminate (powder, containing 37 % Al 2 O) having the composition shown in Table 1.
A chelating agent and a B solution prepared by adding water to blast furnace colloidal cement were prepared. The stability of this B solution at 20°C and the volume ratio of A and B solutions of 1:1.
The unconfined compressive strength measured when gelur time and the cured product were mixed at a ratio of 1:1 and cured in wet sand for 7 days were as shown in Table 1.
【表】【table】
【表】
比較例 1〜6
第2表に示す組成のB液を用いる以外は実施例
1〜4と全く同様にして土質安定剤を調整し、各
ゲル化時間及びゲル化物の強度を測定した。[Table] Comparative Examples 1 to 6 Soil stabilizers were prepared in exactly the same manner as in Examples 1 to 4, except that liquid B having the composition shown in Table 2 was used, and the gelation time and strength of each gelled product were measured. .
【表】
* クエン酸ソーダ
その結果は第2表に示す通りで、B液にアルミ
ン酸ソーダ及びキレート化剤を含まない比較1、
2は夫々高炉コロイドセメント量が同じ実施例
1、2に比較してゲル化物の圧縮強度が著しく劣
り、又B液にアルミン酸ソーダを含むがキレート
化剤を含まない比較例3、4はB液のゲル化時間
が早過ぎて実用に供し得ないものであつた。
又、B液中の水対セメントの割合が小さ過ぎる
比較例5はB液のゲル化時間が短く、流動性が悪
いものであり、逆にその割合が大き過ぎる比較例
6は、A液・B液のゲル化物の圧縮強度が著しく
低いものであつた。
実施例5、6、比較例7
直径5cmの鉄製の円筒中に、豊浦標準砂を約30
cmの長さに充填した。
次いで上部より圧力1Kg/cm2で、第3表に記載
の組成の注入剤液250c.c.を流入せしめ硬化後7日
間密閉状態で養生をし、7日後硬化物を脱型し豊
浦標準砂の固結した体積並びにその一軸圧縮強度
を測定した。[Table] * Sodium citrate The results are shown in Table 2.
In Comparative Examples 2 and 4, the compressive strength of the gelled product was significantly inferior to that of Examples 1 and 2, which had the same amount of blast furnace colloidal cement, and in Comparative Examples 3 and 4, which contained sodium aluminate in liquid B but did not contain a chelating agent. The gelation time of the liquid was too fast to be of practical use. In addition, Comparative Example 5, in which the ratio of water to cement in liquid B is too small, has a short gelation time of liquid B, resulting in poor fluidity; conversely, in Comparative Example 6, in which the ratio of water to cement in liquid B is too large, liquid A. The compressive strength of the gelled product of liquid B was extremely low. Examples 5 and 6, Comparative Example 7 Approximately 30 Toyoura standard sand was placed in an iron cylinder with a diameter of 5 cm.
Filled to cm length. Next, 250 c.c. of the injection solution having the composition shown in Table 3 was poured into the upper part at a pressure of 1 kg/cm 2 and after curing, it was cured in a closed state for 7 days. After 7 days, the cured product was demolded and used as Toyoura standard sand. The consolidated volume of and its unconfined compressive strength were measured.
【表】
その結果は第3表に示す通りで、本発明工法に
よればアルミン酸のアルカリ金属塩を含まない懸
濁型グラウト剤を用いた場合と比較して土壌の固
結した体積及びその一軸圧縮強度が著しく増大す
ることが確認された。[Table] The results are shown in Table 3. According to the method of the present invention, the volume of soil consolidated and its It was confirmed that the unconfined compressive strength increased significantly.
Claims (1)
カリ金属塩、水およびキレート化剤が含有され
てなり、水対セメントの重量比が1〜6である
水懸濁液 上記A、B両液を混合して得られた水性混合液
を土壌に注入することを特徴とする土質の安定化
処理工法。 2 珪酸のアルカリ金属塩がナトリウム塩又はカ
リウム塩である第1項記載の工法。 3 アルミン酸のアルカリ金属塩がナトリウム
塩、カリウム塩又はリチウム塩である第1項又は
第2項記載の工法。 4 キレート化剤の量が水性混合液に対し約0.03
〜約1.5重量%である第1項〜第3項何れか1項
に記載の工法。 5 キレート化剤がオキシ酸、オキシ酸のナトリ
ウム塩及びオキシ酸のカリウム塩のうちの少くと
も1種である第1項〜第4項何れか1項に記載の
工法。 6 オキシ酸が酒石酸又はクエン酸である第5項
記載の工法。[Scope of Claims] 1 Solution A: Aqueous solution of alkali metal salt of silicic acid Solution B: Contains blast furnace colloidal cement, alkali metal salt of aluminate, water, and a chelating agent, and the weight ratio of water to cement is 1 to 1. 6. Aqueous Suspension A soil stabilization treatment method characterized by injecting into the soil an aqueous mixed solution obtained by mixing both the above-mentioned solutions A and B. 2. The method according to item 1, wherein the alkali metal salt of silicic acid is a sodium salt or a potassium salt. 3. The method according to item 1 or 2, wherein the alkali metal salt of aluminic acid is a sodium salt, potassium salt, or lithium salt. 4 The amount of chelating agent is approximately 0.03% of the aqueous mixture.
~ about 1.5% by weight, the method according to any one of paragraphs 1 to 3. 5. The method according to any one of Items 1 to 4, wherein the chelating agent is at least one of an oxyacid, a sodium salt of an oxyacid, and a potassium salt of an oxyacid. 6. The method according to item 5, wherein the oxyacid is tartaric acid or citric acid.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1403882A JPS58132077A (en) | 1982-01-30 | 1982-01-30 | Process for stabilizing soil |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1403882A JPS58132077A (en) | 1982-01-30 | 1982-01-30 | Process for stabilizing soil |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58132077A JPS58132077A (en) | 1983-08-06 |
| JPH0362749B2 true JPH0362749B2 (en) | 1991-09-26 |
Family
ID=11849953
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1403882A Granted JPS58132077A (en) | 1982-01-30 | 1982-01-30 | Process for stabilizing soil |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58132077A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2742432B1 (en) * | 1995-12-15 | 1998-02-06 | Spie Fondations | RIGIDIFICATION ACCELERATOR, GROUT FOR SEALING AND / OR CONSOLIDATION OF SOILS AND CONSTRUCTION MATERIALS RELATING TO SUCH AN ACCELERATOR, METHODS USING SUCH GROUT |
| EP0803560A1 (en) * | 1996-04-26 | 1997-10-29 | UTISOL Technologies AG | Agent and process for soil consolidation and for impermeabilising underground structures |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5155113A (en) * | 1974-11-08 | 1976-05-14 | Nitto Chemical Industry Co Ltd | DOSHITSUANTEIKAHOHO |
| JPS5155112A (en) * | 1974-11-08 | 1976-05-14 | Nitto Chemical Industry Co Ltd | DOSHITSUANTEIKAHO |
| JPS53105810A (en) * | 1977-02-28 | 1978-09-14 | Tokuyama Soda Kk | Additive mixture of seawater with cement hardener* and method of stabilizing nature of soil thereby |
-
1982
- 1982-01-30 JP JP1403882A patent/JPS58132077A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58132077A (en) | 1983-08-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0273445B1 (en) | Chemical grout for ground injection and method for accretion | |
| KR101224848B1 (en) | Compositions for Thixotropic Grout Injection Using Weak Alkaline Sodium Silicate | |
| JP3714586B2 (en) | Solidification material for ground injection | |
| JPH0362749B2 (en) | ||
| JPS5849585B2 (en) | soil stabilization method | |
| JPS5826382B2 (en) | Ground improvement method | |
| JP2003119465A (en) | Ground injection chemicals for liquefaction prevention | |
| JP3205900B2 (en) | Grout material for ground injection | |
| JP3150380B2 (en) | Ground injection agent and its injection method | |
| KR100402456B1 (en) | Ground hardening material | |
| JP3142325B2 (en) | Ground injection agent and its injection method | |
| JP3163191B2 (en) | Method for producing hardened gypsum | |
| JP2001098271A (en) | Ground consolidated material | |
| JPH0770562A (en) | Injection liquid for soil consolidation | |
| JP3101949B2 (en) | Ground injection method | |
| JPS5842228B2 (en) | Doshitsu no Antei Kahouhou | |
| JPS6334198B2 (en) | ||
| JP3425737B2 (en) | Chemical liquid for ground injection | |
| JPH07305061A (en) | Silicate-based grout curing agent and ground stabilization method using the same | |
| JPH0121197B2 (en) | ||
| JP2987625B1 (en) | Ground consolidated material | |
| JPS58174489A (en) | Stabilization method of soil | |
| JP2000109835A (en) | Chemical liquid to be injected in soil | |
| JPS6050839B2 (en) | Method for solidifying and stabilizing peat soil | |
| JPH0143797B2 (en) |