JPS59152985A - Impregnation method for ground - Google Patents
Impregnation method for groundInfo
- Publication number
- JPS59152985A JPS59152985A JP2589083A JP2589083A JPS59152985A JP S59152985 A JPS59152985 A JP S59152985A JP 2589083 A JP2589083 A JP 2589083A JP 2589083 A JP2589083 A JP 2589083A JP S59152985 A JPS59152985 A JP S59152985A
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- solution
- ground
- acid
- silicic acid
- injection
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Abstract
Description
【発明の詳細な説明】
本発明は珪酸のコロイド溶液を用いた地盤注入工法に関
するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a ground injection method using a colloidal solution of silicic acid.
従来、地盤注入のために水ガラスクラウドが用いられて
来た。水ガラスグラウトは液状の珪酸のアルカリ金属塩
であり、これに塩や酸を加えて珪酸ゲルを析出する事に
よって地盤を固結するものである。Traditionally, water glass clouds have been used for ground injection. Water glass grout is a liquid alkali metal salt of silicic acid, and is used to solidify the ground by adding salt or acid to precipitate a silicic acid gel.
しかるに、珪酸のアルカリ金属塩は高アルカリ性を呈し
そのゲル化もアルカリ領域で行なわれるため地下水が長
期にわたってアルカリ性を呈するという問題があった。However, since the alkali metal salt of silicic acid exhibits high alkalinity and gelation occurs in the alkaline region, there is a problem in that groundwater remains alkaline for a long period of time.
この問題を解決するために酸性液中に水ガラスを加えて
水ガラス中のアルカリを除去して得られる酸性珪酸水溶
液とアルカリを合流して中性領域でゲル化させる地盤注
入工法が開発されている。To solve this problem, a ground injection method has been developed in which water glass is added to an acidic solution and the alkali in the water glass is removed, and the alkali is combined with the acidic silicic acid solution to form a gel in a neutral region. There is.
このグラウトは固結物が中性を示し、地下水のpHも変
動せずきわめてすぐれた特性を有する注入材であるが、
強度が弱い事、ゲル化が非常に短いという欠点があった
。This grout is a grouting material with extremely excellent properties, as the solids are neutral and the pH of groundwater does not fluctuate.
It had the disadvantages of low strength and very short gelation time.
即ち、通常、水ガラスグラウトにおける注入液中のSi
n、、の濃度は10重量%以上である事が強度の点から
(固結砂の一軸圧縮強度でl Kp / cy1以上)
必要であるが、5102の濃度が10重量%以上ではゲ
ル化時間が中性領域付近(pHが4〜8)で1分以内、
通常数秒になってしまう。浸透性がよく、かつ地盤中で
分散せずに固結するのに適したゲル時間は30〜120
分である串が経験的に判ってい7ト)が、もしゲル化時
間を中性領域付近で;30〜120分析度を得ようとし
たなら5102の濃度は5重量%以下にしなくてはなら
ず、この濃度では固結砂強度は0、5 i(q / c
rIにも達せず、注入工法(では実用上利用出来ない。That is, usually Si in the injection liquid in water glass grout
From the viewpoint of strength, the concentration of n, , should be 10% by weight or more (the unconfined compressive strength of consolidated sand is l Kp / cy1 or more).
However, when the concentration of 5102 is 10% by weight or more, the gelation time is within 1 minute near the neutral region (pH 4 to 8).
It usually takes a few seconds. The gel time is 30 to 120, which has good permeability and is suitable for solidifying without dispersing in the ground.
7) However, if the gelation time is to be near the neutral range and an analysis degree of 30 to 120 is to be obtained, the concentration of 5102 must be less than 5% by weight. At this concentration, the consolidated sand strength is 0.5 i(q/c
It does not reach rI, and the injection method cannot be used practically.
壕だ、中性領域の水ガラスグラウトは酸性液中に水ガラ
スを加叱2て水ガラス中のアルカリを中和して注入液を
得るものでありから、その注入液中には轟然の事ながら
中和によって生成した中和生成物、即ち、Naイオンや
酸根等が多く残留するが水質保全の点からこれらのNa
イオンや酸根も残存しない注入工法が確立出来ればと九
にすぐれるものはない。Well, the water glass grout in the neutral range is made by adding water glass to an acidic solution to neutralize the alkali in the water glass to obtain the injection liquid, so there are a lot of things in the injection liquid. However, many neutralization products generated by neutralization, such as Na ions and acid radicals, remain, but these Na
Nothing would be better than establishing an injection method that leaves no residual ions or acid roots.
又、酸性液中に水ガラスを加えてうる酸性水ガラス液を
地盤注入工法に用いる方法も知られているが、これは酸
の中に水ガラスを加えて単分子からなる珪酸からコロイ
ド状の珪酸を経てゲル化に到る現象を利用したものであ
り、Sl○2をIQ wt%以上にしてかつゲル化時間
を30分以上の艮いウール化時間の配合をうるにはpH
が3付近の酸性・唄域に調整して注入する必要がある。Another known method is to add water glass to an acidic solution and use it in the ground injection method. It utilizes the phenomenon of gelation through silicic acid, and in order to obtain a formulation with a gelation time of 30 minutes or more and a Sl○2 content of IQ wt% or more, the pH must be
It is necessary to adjust and inject to the acidic/singing range around 3.
本発明の目的は以上の間:辿を解決するために更に発展
した技術を提供するものである。The purpose of the present invention is to provide a further developed technique for solving the above problems.
前述の目的を達成するため、本発明によれば、珪酸のコ
ロイド液に以下の一群と二群に示す添加物をそれぞれ併
せて添加して得られる注入液を地盤に注入する事を特徴
とし、前記二群に示す添加物の添加量は全配合液の2重
量%以下であることを特徴とする。In order to achieve the above object, the present invention is characterized by injecting into the ground an injection liquid obtained by adding additives shown in the following groups 1 and 2 to a silicic acid colloid liquid, respectively, It is characterized in that the amount of the additives shown in the second group is 2% by weight or less of the total blended liquid.
一群:アルカリ金属塩および酸の群から選ばれたーイ重
または複数種。Group 1: One or more selected from the group of alkali metal salts and acids.
二群:多価金属の電解質′物質。Group 2: Polyvalent metal electrolyte substances.
以下、本発明を具体的に詳述する。Hereinafter, the present invention will be specifically explained in detail.
本発明者は珪酸のコロイド溶液(シリカゾル)に多価金
属の電解質物質(多価金属イオンを解離する物質)を混
合すると白濁又は部分的な沈澱が生ずるが、その混合量
が全配合液の二重量%以内ならば混合によって流動性を
保持する溶液が得られ、これを地盤に注入すると強固な
固結体がえられ、特に不均質地盤においてきわめてすぐ
れた注入効果が得られる事に着目し、更に研究をすすめ
た結果以下の現象を見出し本発明を完成した。The present inventor discovered that when a polyvalent metal electrolyte substance (a substance that dissociates polyvalent metal ions) is mixed with a colloidal solution of silicic acid (silica sol), white turbidity or partial precipitation occurs, but the amount of the mixture is about 20% of the total mixed solution. We focused on the fact that if it is within the weight percent, a solution that maintains fluidity can be obtained by mixing, and when this is injected into the ground, a strong solidified body can be obtained, and an extremely excellent injection effect can be obtained, especially in heterogeneous ground. As a result of further research, the following phenomena were discovered and the present invention was completed.
即ち、珪酸のコロイド溶液を主材上する配合液に全配合
液の二重量%以内の多価金属の電解質物質に酸又はアル
カリ金属塩の一種又は複数種を併用する事により
6)数時間から数秒までのゲル化時間のコントロールが
容易に可能になる。That is, by adding one or more types of acids or alkali metal salts to a polyvalent metal electrolyte substance within a double weight percentage of the total blended solution to a blended solution containing a colloidal solution of silicic acid as a main ingredient, 6) from several hours. It becomes possible to easily control the gelation time up to several seconds.
■ 均質なゲルが出来る。■ A homogeneous gel can be produced.
■ 添加物の添加量は微量ですむため地下水の水質に影
響を及ぼさない。■ Additives only need to be added in small amounts, so they do not affect the quality of groundwater.
さらに本発明を詳述すれば次のとおりである。Further details of the present invention are as follows.
本発明における珪酸コロイドとは水ガラスからNaイオ
ンを除去或は低減したものであって、例えば水ガラスを
イオン交換樹脂に通して水ガラス中のNaイオンを除去
するかあるいは水ガラスを硫酸で中和してのちNaイオ
ンや硫酸イオン除去して得られる。The silicate colloid in the present invention is water glass with Na ions removed or reduced. For example, the Na ions in the water glass are removed by passing the water glass through an ion exchange resin, or the water glass is soaked with sulfuric acid. It is obtained by summing and then removing Na ions and sulfate ions.
例えばゼオライト系陽イオン交換体、アンモニウム系イ
オン交換体々どのイオン交換樹脂に水ガラスを通過させ
、生成したシリカゾルを80℃〜90℃の温度でさらに
水ガラスに加え、再び前記イオン交換樹脂に通過してイ
オン交換を行なって得られるものであり、比較釣線すい
な(稀薄な)シリカゾルが得られる。さらに純すいなシ
リカゾルを得るには前述の稀薄なシリカゾルを微アルカ
リ性に調整し、これにさらに前述のシリカゾルを加えな
がら蒸発し、安定化と濃縮を同時に行なう方法、あるい
は、イオン交換後の活性シリカゾルを適当なアルカリの
下に加熱し、これにさらに活性シリカゾルを加えて安定
化する方法等が用いられる4、本発明における珪酸コロ
イド溶液はNaイオンが殆んど分離除去されておりモル
比が10以上である。For example, water glass is passed through an ion exchange resin such as a zeolite-based cation exchanger or an ammonium-based ion exchanger, and the generated silica sol is further added to the water glass at a temperature of 80°C to 90°C, and then passed through the ion exchange resin again. The silica sol is obtained by performing ion exchange using a thin silica sol. In order to obtain even pure silica sol, the dilute silica sol mentioned above is adjusted to be slightly alkaline, and the above-mentioned silica sol is further added to it while evaporating, thereby simultaneously stabilizing and concentrating it. Alternatively, the activated silica sol after ion exchange can be used. In the silicic acid colloid solution of the present invention, most of the Na ions have been separated and removed, and the molar ratio is 10. That's all.
通常、SiO□の含有量は10〜60%(重量)、モル
比(S iOq / Na、O)は50以上、pH値は
8〜10に調整したものが望ましい。Usually, it is desirable that the content of SiO□ is 10 to 60% (by weight), the molar ratio (SiOq/Na, O) is 50 or more, and the pH value is adjusted to 8 to 10.
モル比がjoB下に々ると珪酸コロイドは溶けてし丑い
、珪酸塩の水溶液になってしまう。この場合珪酸コロイ
ドの粒経はほぼ6〜50mμが主となる。珪酸コロイド
の粒経が50mμ以上になると沈澱しやすくなる。When the molar ratio falls below joB, the silicate colloid dissolves and becomes an aqueous solution of silicate. In this case, the grain size of the silicic acid colloid is mainly about 6 to 50 mμ. When the grain size of the silicic acid colloid is 50 mμ or more, it tends to precipitate.
このようにして調整された珪酸コロイドは半永久的に安
定しており、これを注入液として用いる場合、T場から
現場への搬入並びに注入操作の際にゲル化する心配がな
い。この珪1夕のコロイド溶液をそのまま地盤中に注入
してもそれ自体実用時間内にゲル化する事はないので実
用上の固結効果は得られない。The silicic acid colloid prepared in this way is stable semi-permanently, and when used as an injection solution, there is no need to worry about gelation during transport from the T field to the site and during injection operations. Even if this colloidal solution of silica is injected directly into the ground, it will not gel itself within a practical period of time, so no practical consolidation effect will be obtained.
本発明者は地盤注入の素材となるものは注入液を配合す
る直前捷では半永久的に安定である事が必要であるが、
注入液を注入する際にはむしろ一部固形分が浮遊してい
る方が不均質な地盤を幼果的に改良するには望ましい事
に着眼した。The inventor believes that the material for ground injection must be semi-permanently stable immediately before mixing the injection liquid.
We focused on the fact that when injecting liquid, it is preferable for some solids to be suspended in order to improve the uneven ground.
なぜならば、通常、注入地盤は空隙の異なる士が複雑に
介在しているため、粗い部分には固形分が填充し、細い
部分には溶液状の注入物が填充するのが最も望ましい。This is because the injection ground usually has a complex interposition of different voids, so it is most desirable to fill the rough areas with solid content and fill the narrow areas with a solution-like injection material.
このようにすれば浸透性のよい溶液状の注入物は逸脱す
る重々く細い土粒子間に浸透しうる。In this way, the injectable solution in the form of a highly permeable solution can penetrate between the deviating heavy and thin soil particles.
このためには溶液状の注入物と固形分の注入物は分離し
やすく、シかも最終的にはゲル化後は全体的に一体化し
た固結が行なわれるのが望ましい。For this purpose, it is desirable that the solution injected material and the solid injected material be easily separated, and that ultimately, after gelation, they can be consolidated as a whole.
本発明者はこのような目的のために珪酸コロイド溶液と
多価金属の電解質物質の反応に着目して実験した結果以
下の点が判明した。For this purpose, the present inventor conducted experiments focusing on the reaction between a silicate colloid solution and a polyvalent metal electrolyte material, and as a result, the following points were found.
(]、) 珪酸のコロイド溶液に多価金属の電解質物
質を微量加えると、瞬間的に白濁又は自沈を生じ、その
程度は上記塩の添加量が増大する程いちじるしくなるが
、全体が均質にかた丑る事なく、これを混合していると
固形分を含有したま丑いつまでも流動しているためゲル
化時間は不明確となる。(],) When a trace amount of a polyvalent metal electrolyte is added to a colloidal solution of silicic acid, cloudiness or scuttling occurs instantaneously, and the degree of this becomes more severe as the amount of the salt added increases, but the whole solution remains homogeneous. If this is mixed without any interruption, the gelation time becomes unclear because the solid content remains fluid forever.
(2)前記電解質物質の濃度が2%(重量)以内ならば
白濁、自沈或は部分的なゲルを生ずるが、流動性は失わ
れずその−it注入可能であり、かつそれを注入すると
地球中にて溶液と固形分が適度に分離し土中の用い部分
に固形分が填充し、細い部分に溶液分が浸透し、固形分
の8102を中心として全体としてゲル化を生ずるため
すぐれた効果をうる。(2) If the concentration of the electrolyte substance is within 2% (by weight), cloudiness, scuttling, or partial gelation will occur, but the fluidity will not be lost and it can be injected, and if it is injected, it will spread all over the earth. The solution and solid content are appropriately separated, the solid content fills the used part of the soil, the solution permeates into the narrow part, and gelation occurs as a whole centering on the solid content of 8102, resulting in excellent effects. sell.
(3)前記電解質物質の濃度が2%よりも大きくなると
直ちに自沈がいちぢるしく、ミキシングによっても流動
性は得られず、また注入しても脈状が主体となり溶液分
による固結効果が殆んど得られない。(3) When the concentration of the electrolyte substance exceeds 2%, scuttling immediately becomes severe, fluidity cannot be obtained even by mixing, and even if it is injected, veins are mainly formed, and the solidification effect due to the solution content is I don't get much.
珪酸コロイドの濃度がうすくなると前記電解質物質の濃
度が2重量%以上に々つても流動性はあるが珪酸分の殆
んどが電解質と反応して多価金属の珪酸塩からなる固形
分となってし甘うため、それを注入しても固形分以外の
溶液分の固結性がなく、強度は極端に低下し、注入効果
は得られなくなる。When the concentration of the silicic acid colloid becomes dilute, even if the concentration of the electrolyte substance exceeds 2% by weight, it remains fluid, but most of the silicic acid content reacts with the electrolyte and becomes a solid content consisting of silicates of polyvalent metals. Because of this, even if it is injected, the solution other than the solid content will not solidify, the strength will be extremely reduced, and no injection effect will be obtained.
一方、本発明者は種々の研究の結果珪酸のコロイド溶液
と酸又は種々の塩との反応には次のような問題がある事
を見出した。On the other hand, as a result of various studies, the present inventor found that the following problems exist in the reaction between a colloidal solution of silicic acid and an acid or various salts.
■ 珪酸コロイドと酸の反応は中性〜弱酸性付近で最も
短かくなるがゲル化時間を数時間以内に短縮せしめるの
は困難である。(2) The reaction between silicic acid colloid and acid is shortest at neutral to weakly acidic conditions, but it is difficult to shorten the gelation time to within a few hours.
■ 珪酸コロイドとアルカリ金属塩を混合するとゲル化
時間を酸の場合よりも短かくする事が出来るが、それに
は限度がある。■ Mixing a silicic acid colloid with an alkali metal salt can shorten the gelation time compared to the case of an acid, but there is a limit to this.
■ 珪酸コロイドに対して多価金属の電解質を全配合液
の2重量%以内を混合すると直ちに白濁又は自沈を生じ
、これをミキシングする事によって流動性はえられるが
、全体的なゲル化が得られず、明白なゲル化時間も不明
確であるため、ゲル化時間を効果的にコントロールする
事がむずかしい。■ When polyvalent metal electrolyte is mixed with silicic acid colloid in an amount of less than 2% by weight of the total mixed solution, white turbidity or scuttling occurs immediately, and fluidity can be obtained by mixing this, but overall gelation is not achieved. It is difficult to effectively control the gelation time because the gelation time is not clear and the apparent gelation time is unclear.
多価金属塩の含有量が全配合量の2重量%以上の場合は
固形分の量が多くなりすぎて流動性が得られず、また珪
酸コロイドの濃度が低ければ流動性はあるものの、地盤
中における浸透固結効果は殆んど得られない。If the content of polyvalent metal salt is 2% by weight or more of the total blending amount, the amount of solid content will be too large and fluidity will not be obtained.If the concentration of silicate colloid is low, fluidity will be obtained, but the soil There is almost no penetration solidification effect inside.
表−1に実験に用いた珪酸のコロイド液の特性を示し、
表−2,3,4,5に実験結果を示す。Table 1 shows the characteristics of the silicic acid colloid liquid used in the experiment.
Experimental results are shown in Tables 2, 3, 4, and 5.
(配合は重量%)。(Composition is weight %).
−ルが可能である事が判った。- It turned out that it is possible.
以上の実験結果より本発明における多価金属の電解質の
含有量は全配合液の2重量%以下、好ましくは0.00
5〜2重量%である事を必須とする。From the above experimental results, the content of the polyvalent metal electrolyte in the present invention is 2% by weight or less, preferably 0.00% by weight of the total mixed solution.
It is essential that the content be 5 to 2% by weight.
本発明における多価金属の電解質物質とはアルカリ士金
属、アルミニウム、遷移金属、希土類金属等の塩化物、
硫酸塩、リン酸塩、硝酸塩、さらにその水酸化物、酸化
物、セメント(アルミニウムの水酸化物を含む)等多価
金属のイオンを解離する物質を云う。これらは珪酸コロ
イドに作用してコロイドを不安定にし、あるいは多価金
属の珪酸塩を形成するものと考えられる。The polyvalent metal electrolyte material in the present invention refers to chlorides of alkali metals, aluminum, transition metals, rare earth metals, etc.
It refers to substances that dissociate ions of polyvalent metals, such as sulfates, phosphates, nitrates, and their hydroxides, oxides, and cement (including aluminum hydroxide). It is thought that these act on the silicate colloid to make it unstable or to form a polyvalent metal silicate.
本発明に用いる酸は硫酸、塩酸、硝酸、リン酸等の無機
酸;ギ酸、酢酸、コハク酸等の有機酸;塩化アルミニウ
ム、硫酸アルミニウム、リン酸1カルシウム、リン酸1
ナトリウム、硫酸水素ナトリウム、硫酸アルミニウム、
塩化アルミニウム等の酸性塩;ニスエル;アミド類;グ
リオキザール等のアルデヒド;アルカリの存在のもとに
加水分解して酸基を生ずる物質;炭酸ガスのように水溶
液が酸性を呈する物質等であるが、これらに限定するも
のではない。しかしながら、強酸が最も経済的である。Acids used in the present invention include inorganic acids such as sulfuric acid, hydrochloric acid, nitric acid, and phosphoric acid; organic acids such as formic acid, acetic acid, and succinic acid; aluminum chloride, aluminum sulfate, monocalcium phosphate, and monophosphoric acid.
Sodium, sodium hydrogen sulfate, aluminum sulfate,
Acidic salts such as aluminum chloride; Nisel; amides; aldehydes such as glyoxal; Substances that generate acid groups by hydrolysis in the presence of alkali; Substances whose aqueous solution exhibits acidity such as carbon dioxide gas, etc. It is not limited to these. However, strong acids are the most economical.
又、本発明におけるアルカリ金属塩の例としてはアルカ
リ金属の塩化物、塩素酸塩、硫酸塩、アルミン酸塩、炭
酸塩、重炭酸塩、硝酸塩、重硫酸塩、重亜硫酸塩、珪弗
酸塩、珪酸塩、リン酸塩、リン酸水素塩、ピロリン酸塩
、重クロム酸塩、過マンガン酸塩等の無機塩、任意の有
機塩等をあげる事が出来る。In addition, examples of the alkali metal salts in the present invention include alkali metal chlorides, chlorates, sulfates, aluminates, carbonates, bicarbonates, nitrates, bisulfates, bisulfites, and silifluorides. Examples include inorganic salts such as silicates, phosphates, hydrogen phosphates, pyrophosphates, dichromates, permanganates, and any organic salts.
なお、本発明に用いるグラウトは地盤中において、ゲル
化が促進され、かつ白濁、自沈による固形分の存在によ
り逸脱しにくい特性を有しているが、特に地盤の土層の
構成が複雑に変化している場合はこのグラウトを二次注
入材として用いることができ、あらかじめ、−次注入材
を注入領域に注入した後にこれを注入する。The grout used in the present invention has properties that promote gelation in the ground and are difficult to deviate from due to the presence of solids due to cloudiness and scuttling. If so, this grout can be used as a secondary grout, and is injected after the secondary grout has previously been injected into the injection area.
上述した一次注入材としてはセメントや石灰等、カルシ
ウムイオンを解離する電解質物質を含む懸濁液5犠にす
ぐれ)ヱーる。As the above-mentioned primary injection material, a suspension containing an electrolyte substance that dissociates calcium ions, such as cement or lime, is preferred.
実施例1
東京部内の細砂と生砂が複雑に介在した地盤中に表−4
の配合Na9の配合液を3000 を注入して透水試験
を行ない、かつ、掘削して固結状況と固結体の一軸圧縮
強度を調べた。透水試験結果では注入前にk = 3.
5 X 10−3cm/ sec であったものが注入
後はk = 4.5 X ]0−’ cm/θecにな
り充分な止水効果が得られた。Example 1 Table 4 was found in the ground in the Tokyo area where fine sand and green sand are interposed in a complex manner.
A water permeability test was carried out by injecting 3000 ml of a mixed Na9 solution, and excavation was conducted to examine the consolidation status and the unconfined compressive strength of the consolidated body. According to the water permeability test results, k = 3.
After injection, k = 4.5 x]0-' cm/θec, which was 5 x 10-3 cm/sec, and a sufficient water stopping effect was obtained.
又掘削調査の結果では注入口を中心として直径が1.2
〜1.3mのほぼ円柱状で10m3程の固結体がえられ
た。掘削断面を調べたところ、粗砂の部分には白色粒状
の固形分の填充がみられ、細砂部分には溶液部分の配合
液によって固結しているのが認められた。又固結体の一
軸圧縮強度試験を行なったところ、細い土の部分では6
.8Kg/cd、粗い土の部分では7.2Kg/cdの
強度をうる事が出来た。Additionally, the results of the excavation survey show that the diameter around the injection port is 1.2 mm.
A roughly cylindrical solid of ~1.3 m and approximately 10 m3 was obtained. When examining the excavated cross section, it was found that the coarse sand part was filled with white granular solids, and the fine sand part was solidified by the mixed liquid in the solution part. In addition, when we conducted an unconfined compressive strength test of the solidified material, we found that it was 6.
.. We were able to obtain a strength of 8Kg/cd, and 7.2Kg/cd in the coarse soil area.
比較のために表−4の配合Nα36の配合を二重管を用
いて注入した。For comparison, the formulation Nα36 in Table 4 was injected using a double tube.
即ち、A液としてSiO□の20%液を外管管路より、
B液としてCaCl2の5%、97%硫酸を0.2%を
含む配合液を内管管路より送り、注入管先端部で1:1
(容量比)で合流して注入した。注入後掘削したところ
塊状の沈澱物が脈状に広範囲に走っており、部分的な固
結はみられたが全体的な固結はみられず、又透水係数の
明白な改善は得られなかった。That is, a 20% SiO
A mixed solution containing 5% of CaCl2 and 0.2% of 97% sulfuric acid as the B solution is sent from the inner pipe line, and is mixed at a ratio of 1:1 at the tip of the injection pipe.
(volume ratio) and injected. When we excavated the area after the injection, we found that massive precipitates were spread over a wide area in the form of veins, and although some consolidation was observed, no overall consolidation was observed, and no obvious improvement in the hydraulic conductivity was obtained. Ta.
実施例2−
東京部内の砂地盤において表−3配合Nl12と表−4
配合Nα16のグラウトをそれぞれ1.000tづつ注
入して、5mはなれた地点に設けた検査孔の地下水の水
質を、注入前ならびに注入後に測定して比較試験を行な
った。Example 2 - Table-3 mixture Nl12 and Table-4 on sandy ground in Tokyo area
A comparative test was conducted by injecting 1.000 t of grout with a composition Nα16 into each grout, and measuring the quality of groundwater in an inspection hole set 5 m apart before and after the injection.
その結果を表−6に示す。The results are shown in Table-6.
数値は地下水め揮取試料12中のミl)グラム数を示す
。The numerical value indicates the number of milligrams in the groundwater volatilization sample 12.
表−6より本発明は珪酸−コロイド中に含有される塩が
すくないのみならず、添加物の量が微量ですむので地下
水の水質変化は実質的にないと考えてよい。、
上述したように本発明は珪酸コロイド溶液と多価金属塩
を混合した場合、直ちに白濁する事に着目し、多価金属
塩の混合量よりグラウト工法における流動性の関係を見
出し、かつ、更に酸やアルカリ金属塩を併用して均質な
ゲルをつくると共にゲル化時間を任意にコントロールし
え、かつ電解質の添加量が微量ですむ事によシ地下水の
水質の変化を殆んど生じない無公害性グラウトを可能な
らしめたものである。From Table 6, the present invention not only contains less salt in the silicic acid colloid, but also requires only a small amount of additives, so it can be considered that there is virtually no change in the quality of groundwater. As mentioned above, the present invention focused on the fact that when a silicic acid colloidal solution and a polyvalent metal salt are mixed, it immediately becomes cloudy, and discovered the relationship between fluidity in grouting methods from the amount of polyvalent metal salt mixed, and further By using acids and alkali metal salts in combination to create a homogeneous gel, the gelation time can be controlled arbitrarily, and only a small amount of electrolyte is added, so there is almost no change in the quality of groundwater. This makes it possible to use non-polluting grout.
Claims (1)
れぞれ併せて添加して得られる注入液を地盤に注入する
事を特徴とし、前記二群に示す添加物の添加量は全配合
液の2重量%以下であることを特徴とする地盤注入工法
。 一群:アルカリ金属塩お−よび酸の群から選ばれた一種
または複数種。 二群:多価金属の電解質物質。[Claims] It is characterized by injecting into the ground an injection liquid obtained by adding additives shown in the following groups 1 and 2 to a colloidal liquid of silicic acid. A ground injection method characterized by the addition amount being 2% by weight or less of the total mixed liquid. Group 1: One or more selected from the group of alkali metal salts and acids. Group 2: Polyvalent metal electrolyte materials.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2589083A JPS59152985A (en) | 1983-02-18 | 1983-02-18 | Impregnation method for ground |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2589083A JPS59152985A (en) | 1983-02-18 | 1983-02-18 | Impregnation method for ground |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59152985A true JPS59152985A (en) | 1984-08-31 |
JPH0468356B2 JPH0468356B2 (en) | 1992-11-02 |
Family
ID=12178381
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2589083A Granted JPS59152985A (en) | 1983-02-18 | 1983-02-18 | Impregnation method for ground |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59152985A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61159485A (en) * | 1984-12-31 | 1986-07-19 | Kyokado Eng Co Ltd | Grouting material |
JP2005320410A (en) * | 2004-05-07 | 2005-11-17 | Mitsubishi Rayon Co Ltd | Chemical for ground stabilization |
JP2012092186A (en) * | 2010-10-26 | 2012-05-17 | Kyokado Kk | Grouting material and grouting method |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5473407A (en) * | 1977-11-22 | 1979-06-12 | Central Glass Co Ltd | Injection agent for eliminating subsoil pollution |
JPS57164186A (en) * | 1981-04-02 | 1982-10-08 | Onoda Cement Co Ltd | Grouting |
JPS5825440A (en) * | 1981-08-05 | 1983-02-15 | Michizo Yamano | Method for separating metal from ore in low pressure |
-
1983
- 1983-02-18 JP JP2589083A patent/JPS59152985A/en active Granted
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5473407A (en) * | 1977-11-22 | 1979-06-12 | Central Glass Co Ltd | Injection agent for eliminating subsoil pollution |
JPS57164186A (en) * | 1981-04-02 | 1982-10-08 | Onoda Cement Co Ltd | Grouting |
JPS5825440A (en) * | 1981-08-05 | 1983-02-15 | Michizo Yamano | Method for separating metal from ore in low pressure |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61159485A (en) * | 1984-12-31 | 1986-07-19 | Kyokado Eng Co Ltd | Grouting material |
JPH0324515B2 (en) * | 1984-12-31 | 1991-04-03 | Kyokado Eng Co | |
JP2005320410A (en) * | 2004-05-07 | 2005-11-17 | Mitsubishi Rayon Co Ltd | Chemical for ground stabilization |
JP2012092186A (en) * | 2010-10-26 | 2012-05-17 | Kyokado Kk | Grouting material and grouting method |
Also Published As
Publication number | Publication date |
---|---|
JPH0468356B2 (en) | 1992-11-02 |
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