JPS62290790A - Grout for injection into ground - Google Patents

Grout for injection into ground

Info

Publication number
JPS62290790A
JPS62290790A JP13371686A JP13371686A JPS62290790A JP S62290790 A JPS62290790 A JP S62290790A JP 13371686 A JP13371686 A JP 13371686A JP 13371686 A JP13371686 A JP 13371686A JP S62290790 A JPS62290790 A JP S62290790A
Authority
JP
Japan
Prior art keywords
calcium
alkaline
gelation
magnesium
gelation time
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
Application number
JP13371686A
Other languages
Japanese (ja)
Other versions
JPH0643582B2 (en
Inventor
Shunsuke Shimada
俊介 島田
Kenji Kashiwara
栢原 健二
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kyokado Engineering Co Ltd
Original Assignee
Kyokado Engineering Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Kyokado Engineering Co Ltd filed Critical Kyokado Engineering Co Ltd
Priority to JP61133716A priority Critical patent/JPH0643582B2/en
Publication of JPS62290790A publication Critical patent/JPS62290790A/en
Publication of JPH0643582B2 publication Critical patent/JPH0643582B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

PURPOSE:To facilitate the control of a long gelation time and, at the same time, to improve the strength of the neutral region of an agglomerate, by blending an aq. non-alkaline silicic acid soln. with calcium salt or magnesium salt of phosphoric acid. CONSTITUTION:A grout prepd. by blending an aq. alkaline silicic acid soln., obtd. by treating water glass with an acid, with calcium or magnesium salt of phosphoric acid. The calcium phosphate or magnesium phosphate, particularly dibasic calcium phosphate and dibasic magnesium phosphate have outstanding features that they not only exhibit an effect of promoting the gelation of the aq. non-alkaline silicic soln. despite the fact that they are slightly soluble in water and neutral or slightly acidic but also do not decrease the gelation time to less than several ten minutes or ten-odd minutes.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は軟弱あるいは漏水地盤の固結あるいは止水に用
いられる非アルカリ性珪酸水溶液を用いた地盤注入用薬
液に係り、特にゲル化時間の調整が容易であって固結物
が中性で、かつ高強度を呈する地盤注入用薬液に関する
[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a chemical solution for ground injection using a non-alkaline silicic acid aqueous solution used to solidify or stop water in soft or leaky ground, and in particular to adjustment of gelation time. The present invention relates to a chemical solution for ground injection that is easy to prepare, has a neutral solidified substance, and exhibits high strength.

〔従来の技術〕[Conventional technology]

非アルカリ性珪酸水溶液は水ガラスと酸を混合して水ガ
ラス中のアルカリを除去して得られるもので、通常は酸
性液と水ガラス水溶液を噴射あるいは強制的に攪拌混合
することにより調製され、pH1〜3の強酸性珪酸水溶
液である。
A non-alkaline silicic acid aqueous solution is obtained by mixing water glass and an acid to remove the alkali in the water glass.It is usually prepared by spraying or forcibly stirring and mixing the acidic liquid and the water glass aqueous solution, and the pH is 1. -3 strongly acidic silicic acid aqueous solution.

この非アルカリ性珪酸水溶液を地盤注入用薬液として用
いる場合、これはゲル化時間が長いので、通常、この水
溶液にアルカリ性促進剤を添加混合し、ゲル化を促進せ
しめて用いられる。このアルカリ性促進剤として従来、
水ガラス液、苛性アルカリ、炭酸塩9重炭酸塩等が用い
られている。
When this non-alkaline silicic acid aqueous solution is used as a chemical solution for ground injection, since it takes a long time to gel, an alkaline accelerator is usually added to the aqueous solution to promote gelation. Conventionally, as this alkaline accelerator,
Water glass liquid, caustic alkali, carbonate 9 bicarbonate, etc. are used.

又、ゲル化時間をゆるやかにするために、炭酸カルシウ
ム、炭酸マグネシウム、水酸化カルシウム、水酸化マグ
ネシウム等の難溶性アルカリ剤を用いる方法も知られて
いる。
Also known is a method of using a sparingly soluble alkali agent such as calcium carbonate, magnesium carbonate, calcium hydroxide, magnesium hydroxide, etc. in order to slow down the gelation time.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

しかし、前者の方法では、このような従来のアルカリ性
促進剤の僅かな量的変化に対してゲル化時間が大幅に変
動するため、ゲル化時間の調整が非常に困難である。
However, in the former method, it is very difficult to adjust the gelation time because the gelation time varies greatly in response to such a slight quantitative change in the conventional alkaline accelerator.

また、後者の方法では、難溶性アルカリ剤の添加量が多
くなるとゲル化時間が大巾に短縮し、かつゲル化物はア
ルカリ性を呈するという欠点があった。又炭酸塩を用い
た場合、炭酸ガスを発生して固結物がポーラスになり、
強度が弱くなるという欠点があった。
In addition, the latter method has the disadvantage that when the amount of the sparingly soluble alkaline agent added increases, the gelation time is significantly shortened and the gelled product exhibits alkalinity. In addition, when carbonate is used, carbon dioxide gas is generated and the solidified material becomes porous.
The drawback was that the strength was weakened.

本発明の目的は、前述の公知技術に存する欠点を改良し
たもので、特に長いゲル化時間の調整が容易であるとと
もに固結体が中性領域において高強度を呈するような地
盤注入用薬液を提供することにある。
The object of the present invention is to improve the drawbacks of the above-mentioned known techniques, and to provide a chemical solution for ground injection that is particularly easy to adjust for a long gelation time and that allows the solidified body to exhibit high strength in the neutral region. It is about providing.

〔問題点を解決するための手段〕[Means for solving problems]

前述の目的を達成するため、本発明によれば、水ガラス
を酸で処理して得られる非アルカリ性珪酸水溶液と、リ
ン酸のカルシウム塩またはマグネシウム塩とを含有して
なることを特徴とする。
In order to achieve the above object, the present invention is characterized in that it contains a non-alkaline silicic acid aqueous solution obtained by treating water glass with an acid, and a calcium salt or magnesium salt of phosphoric acid.

本発明に用いられる非アルカリ性珪酸水溶液は水ガラス
水溶液と酸を混合して水ガラス中のアルカリを除去して
得られるものであり、通常はpH1〜3の強酸性を呈す
るものである。
The non-alkaline silicic acid aqueous solution used in the present invention is obtained by mixing a water glass aqueous solution and an acid to remove the alkali in the water glass, and usually exhibits strong acidity with a pH of 1 to 3.

本発明に用いるリン酸塩は、第一、第二、第三等のリン
酸のカルシウム塩、またはマグネシウム塩である事が必
要であって、その他の塩例えば、第一、第二、第三リン
酸塩ナトリウム等のリン酸アルカリ金属塩では本発明の
効果は得られない。
The phosphate used in the present invention must be a calcium salt or a magnesium salt of primary, secondary, or tertiary phosphoric acid; The effects of the present invention cannot be obtained with alkali metal phosphates such as sodium phosphate.

第三リン酸ナトリウム、第ニリン酸ナトリウムはアルカ
リ性を呈し、添加量ゲル化時間曲線は他のアルカリ剤に
くらべればゆるやかであるが添加量が多くなればゲル化
時間が数十秒以内になってしまう。
Sodium triphosphate and sodium diphosphate exhibit alkalinity, and the gelation time curve of the added amount is gentler than that of other alkaline agents, but as the amount added increases, the gelation time decreases to within tens of seconds. Put it away.

又第一リン酸ナトリウムは酸性を呈し、これは非アルカ
リ性珪酸水溶液中に加えてもゲル化促進作用はあまり生
じない。
In addition, monobasic sodium phosphate exhibits acidity, and even when added to a non-alkaline silicic acid aqueous solution, it does not significantly promote gelation.

これに対し、本発明にかかるリン酸カルシウム、または
マグネシウム、特に第ニリン酸カルシウム。
In contrast, calcium or magnesium phosphate, in particular calcium diphosphate, according to the invention.

第ニリン酸マグネシウムは僅かに水溶性で中性から微酸
性を呈しているにもかかわらず非アルカリ性珪酸水溶液
のゲル化促進効果を有し、しかも多量に加えても、ゲル
化時間は数十分あるいは十数分収下よりも短縮しないと
いう大きな特徴を有している。
Although magnesium diphosphate is slightly water-soluble and exhibits neutral to slightly acidic properties, it has the effect of promoting gelation of non-alkaline silicic acid aqueous solutions, and even when added in large amounts, the gelation time is several tens of minutes. It also has the great feature that it does not shorten more than 10 minutes or less.

この理由はカルシウムイオン又はマグネシウムイオンが
ゲル化促進作用を有し、かつその水溶液のpH値が中性
から微酸性であることからゲル化曲線の傾斜を極めてゆ
るやかにし、しかもゲル化時間をある時間以内には短縮
させないという効果を生じ、さらにゲル化物のpit値
を弱酸性から中性に保ちアルカリ領域には達せしめない
というきわめて特異な効果を生じさせるものと思われ、
このような効果は本出願人によってはじめて発見された
ものである。
The reason for this is that calcium ions or magnesium ions have a gelation-promoting effect, and the pH value of the aqueous solution is neutral to slightly acidic, so the slope of the gelation curve is extremely gentle, and the gelation time is It is believed that this has the effect of not shortening the gel within the range of 100 to 100%, and also has the very unique effect of keeping the pit value of the gel from weakly acidic to neutral and preventing it from reaching the alkaline range.
This effect was first discovered by the applicant.

〔実施例〕〔Example〕

以下、本発明を第ニリン酸カルシウムを用いて説明する
Hereinafter, the present invention will be explained using calcium diphosphate.

実験−1 表−1に示した配合により非アルカリ性珪酸水溶液を作
製した。
Experiment-1 A non-alkaline silicic acid aqueous solution was prepared according to the formulation shown in Table-1.

表−1 実験−2 実験−1の非アルカリ性珪酸水溶液(1)、(2150
ccをそれぞれ用意し、これらをA液とした。
Table-1 Experiment-2 Non-alkaline silicic acid aqueous solution (1) of Experiment-1, (2150
cc were prepared, and these were used as liquid A.

さらに第ニリン酸カルシウム量を変化させてそれぞれ水
で50ccの懸濁液とし、これをB液とした。
Further, the amount of calcium diphosphate was varied and each suspension was made into a 50 cc suspension with water, which was designated as Solution B.

これらA液およびB液を合流し、合流液についてゲル化
時間とpHを測定し、結果を第1図および第2図のグラ
フに示した。
These solutions A and B were combined, and the gelation time and pH of the combined solution were measured, and the results are shown in the graphs of FIGS. 1 and 2.

図中、曲線Aは合流直後のpHを、曲線Bはゲル化して
1日経過した後の固結体のpHを示す。
In the figure, curve A shows the pH immediately after confluence, and curve B shows the pH of the solidified body one day after gelation.

第1図および第2図から、注入に最も適したゲル化時間
である数十分から数分の範囲において、安定したゲル化
時間を得ることがわかる。また、合流液は合流直後、曲
線Aのとおり酸性乃至弱酸性のpH値を呈するが、ゲル
化後は曲線Bのとおり、pH5乃至中性を呈し、本発明
薬液はほとんど無公害グラウトであることがわかる。
It can be seen from FIGS. 1 and 2 that a stable gelation time can be obtained in the range of several tens of minutes to several minutes, which is the most suitable gelation time for injection. In addition, the combined liquid exhibits an acidic to slightly acidic pH value as shown in curve A immediately after the confluence, but after gelation, as shown in curve B, it exhibits a pH of 5 to neutral, which means that the chemical solution of the present invention is almost pollution-free grout. I understand.

この結果より、本発明ではきわめて安定した長いゲル化
時間の調整が可能であり、またA液・B液の吐出量のば
らつきによる注入操作の誤差や配合誤差があってもゲル
化時間の変動の少い注入が可能となる事が判る。
From this result, it is possible to adjust an extremely stable long gelation time with the present invention, and even if there is an error in the injection operation or a mixing error due to variations in the discharge amount of liquids A and B, fluctuations in the gelation time can be suppressed. It can be seen that a small amount of injection is possible.

実験−3 比較のために種々の添加剤を用いた実験の例を表−2に
示す。
Experiment 3 Table 2 shows examples of experiments using various additives for comparison.

表−2 (温度18〜20℃) 表−2の結果から本発明に係る第ニリン酸カル  −シ
ウム、第ニリン酸マグネシウムの場合(配合隘15〜2
0)は他の添加剤に比べて、添加量によ  ゛るゲル化
時間の変動が極めて少く安定化している  −ことがわ
かる。
Table 2 (Temperature 18 to 20°C) From the results in Table 2, in the case of calcium diphosphate and magnesium diphosphate according to the present invention (composition range 15 to 2
It can be seen that, compared to other additives, the gelation time of 0) has extremely little variation depending on the amount added and is stable.

実験−41 表−2の配合液を標準砂と混合して固結せしめた、固結
標準砂の一軸圧縮強度を表−3に示す。
Experiment 41 Table 3 shows the unconfined compressive strength of consolidated standard sand, which was obtained by mixing the blended solution in Table 2 with standard sand and consolidating it.

表−3す る 表−3の結果から表−2の配合番号16.19(本発明
)の第ニリン酸カルシウム2第ニリン酸マグネシウムの
場合は他の場合に比べ高い強度を  1斥していること
がわかる。
From the results in Table 3, it can be seen that the calcium diphosphate dimagnesium diphosphate of combination number 16.19 (invention) in Table 2 has a higher strength than other cases. Recognize.

なお、本発明にかかるリン酸のカルシウム塩。In addition, the calcium salt of phosphoric acid according to the present invention.

ングネシウム塩は第ニリン酸塩に限らず第一、第三リン
酸塩においてもはパ同様な結果が得られる。
Similar results can be obtained with ngnesium salts, not only with diphosphates but also with primary and tertiary phosphates.

また、第一、第二および第三リン酸塩は互いに洋用して
用いてもよい。
Furthermore, primary, secondary and tertiary phosphates may be used interchangeably.

なお、本発明にかかる薬液を実際に地盤中に注(するに
当って、例えば水ガラスと酸を混合してlられた、pH
が3以下の非アルカリ性珪酸水溶液二前記リン酸塩を添
加混合し、この混合物を地盤−に注入することはもちろ
んのこと、前記非アル5り性珪酸水溶液にリン酸塩水溶
液を合流して注(することもできる。(合流液のpH値
は酸性でも、ビルカリ性でも、中性でもよい。) さらに、例えば二重注入管を用い、一方の管路)1ら非
アルカリ性珪酸水溶液あるいはこれにリン変温を含む混
合物を送液し、他方の管路から水ガラス、アルカリ性塩
、セメント、その他のアルカノ類を送液し、注入管、先
端部でこれらを合流して輝粘性グラウトとして注入し、
その後リン酸塩水溶液あるいはこれに塩やアルカリ性促
進剤を配合し、この配合液を前記非アルカリ性珪酸水溶
液の注入系統の任意の個所で合流して、ゲル化時間の長
い浸透性グラウトとして注入し、本発明薬液を複合注入
工法の薬液として利用することもできる。
In addition, when actually pouring the chemical solution according to the present invention into the ground, for example, the pH
Of course, it is possible to add and mix the above-mentioned phosphate with a non-alkaline aqueous silicic acid solution having an alkali of 3 or less, and to inject this mixture into the ground. (The pH value of the combined liquid may be acidic, bilcalicic, or neutral.) Furthermore, for example, by using a double injection pipe, one pipe may be used. A mixture containing phosphorus is delivered, and water glass, alkaline salts, cement, and other alkanoids are delivered from the other pipe, and these are combined at the tip of the injection pipe and injected as bright viscous grout. ,
Thereafter, a phosphate aqueous solution or a salt or an alkaline accelerator are mixed therein, and this mixed solution is combined at any point in the injection system of the non-alkaline silicic acid aqueous solution and injected as a permeable grout with a long gelling time, The chemical solution of the present invention can also be used as a chemical solution for a composite injection method.

〔発明の効果〕〔Effect of the invention〕

以上のとおり本発明にかかる地盤注入用薬液は非アルカ
リ性珪酸水溶液と、リン酸のカルシウム塩又はマグネシ
ウム塩を含有してなるから長時間のゲル化時間領域の調
整が容易であるとともに固結強度が大きく、地下水のp
Hも大きく変化せしめることなく実用上有用な薬液であ
る。
As described above, since the chemical solution for ground injection according to the present invention contains a non-alkaline silicic acid aqueous solution and a calcium salt or magnesium salt of phosphoric acid, it is easy to adjust the long gelation time range and the consolidation strength is high. large, groundwater p
It is a practically useful chemical solution without significantly changing H.

【図面の簡単な説明】[Brief explanation of drawings]

第1図および第2図は非アルカリ性珪酸水溶液と対する
第ニリン酸カルシウムの添加量と、それに対応したp)
Iおよびゲル化時間の変化を表わしたグラフである。 写10
Figures 1 and 2 show the amount of calcium diphosphate added to the non-alkaline silicic acid aqueous solution and the corresponding p)
1 is a graph showing changes in I and gelation time. Picture 10

Claims (1)

【特許請求の範囲】[Claims] 水ガラスを酸で処理して得られる非アルカリ性珪酸水溶
液と、リン酸のカルシウム塩又はマグネシウム塩とを含
有してなる地盤注入用薬液。
A chemical liquid for ground injection containing a non-alkaline silicic acid aqueous solution obtained by treating water glass with an acid and a calcium salt or magnesium salt of phosphoric acid.
JP61133716A 1986-06-11 1986-06-11 Ground injection chemical Expired - Lifetime JPH0643582B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61133716A JPH0643582B2 (en) 1986-06-11 1986-06-11 Ground injection chemical

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61133716A JPH0643582B2 (en) 1986-06-11 1986-06-11 Ground injection chemical

Publications (2)

Publication Number Publication Date
JPS62290790A true JPS62290790A (en) 1987-12-17
JPH0643582B2 JPH0643582B2 (en) 1994-06-08

Family

ID=15111232

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61133716A Expired - Lifetime JPH0643582B2 (en) 1986-06-11 1986-06-11 Ground injection chemical

Country Status (1)

Country Link
JP (1) JPH0643582B2 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6363785A (en) * 1986-09-05 1988-03-22 Kyokado Eng Co Ltd Grout for ground
JP2001348572A (en) * 2000-06-07 2001-12-18 Nagoya Cullet Kk Method of solidifying ground foundation
JP2002155279A (en) * 2000-11-22 2002-05-28 Nagoya Cullet Kk Method for hardening ground
JP2003531798A (en) * 2000-04-28 2003-10-28 ブレント アール. コンスタンツ, Calcium phosphate cement prepared from silicate solution
US7776413B2 (en) 2002-09-10 2010-08-17 Yupo Corporation Melt thermal transfer recording paper

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52126912A (en) * 1976-04-19 1977-10-25 Kyokado Eng Co Method of stabilizing poor subsoil
JPS5473407A (en) * 1977-11-22 1979-06-12 Central Glass Co Ltd Injection agent for eliminating subsoil pollution
JPS59124986A (en) * 1982-12-31 1984-07-19 Kyokado Eng Co Ltd Solidification of ground

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52126912A (en) * 1976-04-19 1977-10-25 Kyokado Eng Co Method of stabilizing poor subsoil
JPS5473407A (en) * 1977-11-22 1979-06-12 Central Glass Co Ltd Injection agent for eliminating subsoil pollution
JPS59124986A (en) * 1982-12-31 1984-07-19 Kyokado Eng Co Ltd Solidification of ground

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6363785A (en) * 1986-09-05 1988-03-22 Kyokado Eng Co Ltd Grout for ground
JPH0587554B2 (en) * 1986-09-05 1993-12-17 Kyokado Eng Co
JP2003531798A (en) * 2000-04-28 2003-10-28 ブレント アール. コンスタンツ, Calcium phosphate cement prepared from silicate solution
JP2001348572A (en) * 2000-06-07 2001-12-18 Nagoya Cullet Kk Method of solidifying ground foundation
JP4507355B2 (en) * 2000-06-07 2010-07-21 名古屋カレット株式会社 Ground hardening method
JP2002155279A (en) * 2000-11-22 2002-05-28 Nagoya Cullet Kk Method for hardening ground
JP4507393B2 (en) * 2000-11-22 2010-07-21 名古屋カレット株式会社 Ground hardening method
US7776413B2 (en) 2002-09-10 2010-08-17 Yupo Corporation Melt thermal transfer recording paper
US8268415B2 (en) 2002-09-10 2012-09-18 Yupo Corporation Melt thermal transfer recording paper

Also Published As

Publication number Publication date
JPH0643582B2 (en) 1994-06-08

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