JPS58174489A - Stabilization method of soil - Google Patents
Stabilization method of soilInfo
- Publication number
- JPS58174489A JPS58174489A JP5928382A JP5928382A JPS58174489A JP S58174489 A JPS58174489 A JP S58174489A JP 5928382 A JP5928382 A JP 5928382A JP 5928382 A JP5928382 A JP 5928382A JP S58174489 A JPS58174489 A JP S58174489A
- Authority
- JP
- Japan
- Prior art keywords
- water
- soil
- bicarbonate
- weight
- gelling agent
- 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】
本発明は改良された水ガラス系グラウトによる土質安定
化方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for stabilizing soil quality using an improved water glass grout.
従来、軟弱地盤の強化あるいは湧水地盤の止水のために
種々の薬液を地盤に注入し、地盤中でゲル化させる薬液
注入工法が知られているが、安定性等の面からケイ酸ソ
ーダを主剤としこれにゲル化剤を配した水ガラス系グラ
ウトが広く実用化されている。薬液注入工法においては
最近ではゲルタイムが数秒から士数秒の瞬結タイプのグ
ラウトが要求されており、これは従来のゲルタイムが数
分から数十分のグラウトでは地下水流の多い場所や砂礫
の多い地層に使用した場合、ゲル化する以前に希釈され
て流出したり、不必要な範囲まで薬液が浸透して地盤の
改良が不完全になったり公害面で悪影響を及ぼすためで
ある。しかしながら瞬結タイプのグラウトはゲルタイム
が不安定で部分的にゲル化を起し易く不均一なゲルとな
り白濁現象やゲル−液分離現象を生ずることが多い。そ
れ故ゲルタイムの調整が困難となり注入地盤の強度を低
下させる原因となる。特に夏季は水温が高くなるためそ
の傾向が強い。要するにゲルタイムが短いというのみで
なく、年間を通じて安定したゲルタイムを持も均一なゲ
ルを形成し得ることが上質に適した改良を行うために必
要ぐある。Conventionally, chemical injection methods have been known in which various chemical solutions are injected into the ground and gelled in the ground in order to strengthen soft ground or stop water from spring water. Water glass grout, which has a gelling agent added to it as a main ingredient, has been widely put into practical use. In the chemical injection method, there has recently been a demand for instant setting type grout with a gel time of several seconds to several seconds.This means that conventional grouts with a gel time of several minutes to several tens of minutes are difficult to install in places with a lot of underground water flow or in strata with a lot of sand and gravel. This is because when used, the chemical solution may be diluted and flowed out before gelatinization, or the chemical solution may penetrate into unnecessary areas, resulting in incomplete ground improvement and adverse effects on pollution. However, instant setting type grout has an unstable gel time and tends to partially gel, resulting in an uneven gel that often causes cloudiness and gel-liquid separation. Therefore, it becomes difficult to adjust the gel time, which causes a decrease in the strength of the injection ground. This tendency is particularly strong in the summer as the water temperature rises. In short, it is necessary not only to have a short gel time, but also to be able to form a uniform gel with a stable gel time throughout the year in order to improve the quality.
土質安定化のゲル化剤として重炭酸アルカリのみを用い
た場合は浸透したゲル化体がゲル化後1夜のうちに元の
体積の80%以下、数日後に50%以下にゲルが収縮し
土層の体積は変らないため、土層がポーラスとなり止水
性が低下するとともに浸透した水にゲル成分が溶解して
もろくなり水中強度が急激に低下する。When only alkali bicarbonate is used as a gelling agent for soil stabilization, the infiltrated gelatinized material shrinks to less than 80% of its original volume overnight after gelation, and to less than 50% a few days later. Since the volume of the soil layer does not change, the soil layer becomes porous, reducing its water-stopping properties, and the gel component dissolves in the water that permeates, causing it to become brittle, and its underwater strength rapidly decreases.
本発明は水ガラスおよびそのゲル化剤を使用して土質を
安定化するにあたり、主剤として重炭酸アルカリを使用
し、これとマグネシウム塩、クエン酸塩を併用すること
により安定なゲル化を行うとともに上記の収縮性および
水中強度の低下を改良する方法を提供するものである。The present invention uses water glass and its gelling agent to stabilize soil quality, uses alkali bicarbonate as the main agent, and uses this together with magnesium salt and citrate to achieve stable gelation. The object of the present invention is to provide a method for improving the above-mentioned decrease in shrinkage and strength in water.
すなわち本発明は固形分10〜40重−%のケイ酸ソー
ダ溶液と、ゲル化剤として重炭酸ソーダおよび/または
重炭酸カリ 100重量部に対しマグネシウムの硫酸塩
、塩化物の単独または混合物(無水物換専)5〜100
重量部、クエン酸のソーダ塩、カーリ・ラム塩の単独ま
たは混合物3〜200重量部よりなる成分60〜350
g / lを含む薬液とを土壌に注入し、硬化させるこ
とを特徴とする土質安定化方法である。重炭酸アルカリ
をゲル化剤として使用する場合の収縮性を改善する試み
としてマグネシウム塩を併用する2成分系が知られてい
る(特公昭53’ −43247号、特公昭56−21
778号)。しかしながらマグネシウム塩のみでは不均
一なゲル化を起しやすく夏季の高い液温においての使用
には適さない。そのためマグネシウム塩を収縮性改良に
効果を持つ程多量に配合する場合は冷却を要するかまた
は寒冷地等の特殊な地域の使用に限られてくる。他方重
炭酸アルカリを使用せずにアルミニウム堪、マグネシウ
ム塩とともにクエン酸、酒石酸、乳酸等のオキシ酸を使
用して他成分の金属イオンと結合りるキレート作用を利
用した方法が知られている(特公昭53−24724号
)。しかしながらこのタイプのゲル化剤はゲルタイムの
調整が困難であって安定した瞬結タイプの薬剤にはなり
難い。キレート化剤としては伯にリン酸塩系統のものが
知られるが瞬結タイプのゲル化安定剤として使用した場
合、水ガラスと混合する以前に薬液が白濁することがあ
って実用化にはさらに多くの検討が必要である。That is, the present invention uses a sodium silicate solution having a solid content of 10 to 40% by weight, 100 parts by weight of sodium bicarbonate and/or potassium bicarbonate as a gelling agent, and magnesium sulfate or chloride alone or as a mixture (anhydrous chloride). Specialty) 5-100
60 to 350 parts by weight, consisting of 3 to 200 parts by weight of soda salt of citric acid, kali rum salt alone or in a mixture
This is a soil stabilization method characterized by injecting a chemical solution containing 1 g/l into the soil and hardening it. In an attempt to improve shrinkage when alkali bicarbonate is used as a gelling agent, a two-component system using a magnesium salt in combination is known (Japanese Patent Publication No. 53'-43247, Japanese Patent Publication No. 56-21).
No. 778). However, magnesium salt alone tends to cause uneven gelation and is not suitable for use at high liquid temperatures in summer. Therefore, when magnesium salt is incorporated in a large enough amount to be effective in improving shrinkage, cooling is required or use is limited to special regions such as cold regions. On the other hand, there is a known method that uses oxyacids such as citric acid, tartaric acid, and lactic acid together with aluminum salts and magnesium salts, without using alkali bicarbonate, to utilize the chelating effect of binding with other metal ions ( Special Publication No. 53-24724). However, it is difficult to adjust the gel time of this type of gelling agent, and it is difficult to obtain a stable instant-setting type drug. Phosphate-based chelating agents are known, but when used as instant-setting type gelling stabilizers, the chemical solution may become cloudy before being mixed with water glass, making it difficult to put it into practical use. Much consideration is required.
本発明においてはゲル化の安定剤としてクエン酸アルカ
リを使用するが、クエン酸そのものは溶解時の発泡のた
め使用できずまた他のオキシカルボン酸のアルカリ塩た
とえば酒石酸ナトリウムまたはグルコン酸ナトリウムは
不均一なゲルを生成し不適当である。使用薬液の配合比
は第1図で示されるDEFGの範囲内であり、X範囲内
では不均一グルの生成を防ぎ得ず、Yの範囲内ではゲル
タイムが長くなり瞬結タイプになり難いと同時にゲルの
強度も小さい。またZの範囲内ではゲルの収縮が著しく
水中強度が小さくなりWの範囲内ぐは不均一ゲルが生成
しやすい。経済性の面から特に好ましいのは第1図のH
IJKの範囲内寸なわら重炭酸アルカリ 100重量部
に対しマグネシウムの塩化物および/またはfi7AF
IJ塩10〜40重饋部、クエン酸アルカリ 5〜12
0重爆部である。In the present invention, alkali citrate is used as a stabilizer for gelation, but citric acid itself cannot be used because it foams when dissolved, and other alkali salts of oxycarboxylic acids, such as sodium tartrate or sodium gluconate, are not uniformly used. It is unsuitable because it produces a gel. The compounding ratio of the chemical solution used is within the range of DEFG shown in Figure 1; within the range of The strength of the gel is also low. Further, within the range of Z, the gel shrinks significantly and its strength in water becomes low, and within the range of W, a non-uniform gel is likely to be formed. Particularly preferable from the economic point of view is H in Figure 1.
Magnesium chloride and/or fi7AF per 100 parts by weight of alkali bicarbonate within the range of IJK
IJ salt 10-40 parts, alkali citrate 5-12
It is a 0 heavy bomb.
土質安定化の施工は従来と同じであって施工前に、ケイ
酸ソーダ水溶液と上記配合の薬液とを別個に調整してお
いて両液を二重管等を用いてポンプで土壌中に圧入する
−またこの薬液の成分濃麿は薬液11中に60〜350
g特に80〜250gが好ましく60g未満では強度の
あるケイ酸ゲルを析出し難く350gをこえると溶解性
が悪くなりまた経済面で不適当である。ケイ酸ソーダ濃
度はHa20とSL O2の固形分が10〜40重量%
が好適で10重量%未満では固結強度が充分でなり40
重量%をこえると粘度が上昇して地盤への浸透性等の面
で難点がある。またその5LO2/Na2Oモル比は1
.5〜4.0の範囲であれば使用しうるが特にJIS3
号水ガラスが入手しやすく好ましい。The soil stabilization work is the same as before; before construction, a sodium silicate aqueous solution and the above-mentioned chemical solution are prepared separately, and both solutions are injected into the soil with a pump using a double pipe, etc. - Also, the component concentration of this drug solution is 60 to 350 in drug solution 11.
g is particularly preferably 80 to 250 g; if it is less than 60 g, it will be difficult to precipitate a strong silicic acid gel, and if it exceeds 350 g, the solubility will deteriorate and it is also unsuitable from an economical point of view. Sodium silicate concentration is Ha20 and SL O2 solid content is 10-40% by weight
is preferable, and if it is less than 10% by weight, the consolidation strength is sufficient and 40
If it exceeds % by weight, the viscosity will increase and there will be problems in terms of permeability into the ground. Also, the 5LO2/Na2O molar ratio is 1
.. It can be used as long as it is within the range of 5 to 4.0, but especially JIS3
No. water glass is preferred because it is easily available.
以上のように本発明方法によれば重炭酸アルカリを水ガ
ラスのゲル化剤とした瞬結タイプのグラウトとして、特
定範囲のマグネシウム硫酸塩、塩化物により収縮性を改
良し、これに特定範囲のクエン酸アルカリを併用するこ
とにより四季を通じてゲル化の際の安定性を著しく向上
することができ水中強度も改善されるので産業上の利用
価値が大である。As described above, according to the method of the present invention, an instant setting type grout using alkali bicarbonate as a gelling agent for water glass is produced, and its shrinkage is improved with a specific range of magnesium sulfate and chloride. By using alkali citrate in combination, the stability during gelation can be significantly improved throughout the seasons, and the strength in water is also improved, so it has great industrial value.
以下実施例、比較例により本発明の効果を示す。The effects of the present invention will be illustrated below with reference to Examples and Comparative Examples.
なお例において薬剤量は全て無水物換算である。In the examples, all drug amounts are calculated on an anhydride basis.
実施例、比較例 JIsa号ケイ酸ソーダ(Ha209.5%。Examples, comparative examples JIsa No. Sodium Silicate (Ha209.5%.
5L0229%)50■Cに水50箇ρを加えA液とす
る。Add 50 parts of water to 5L0229%) 50■C to prepare solution A.
また下記表中の薬剤を水に溶解して 100■Cとしこ
れをB液とする。等容量のA液とB液とを混合しゲル化
温度、ゲル化状況、ゲルタイムを測定した結果を第1表
に示す。またA液、B液の等容量混合液を15℃にて1
夜放置した後の小モゲルについて体積および一軸圧縮強
度を第2表に示す。 ′1′:第
1 表
注・・・第1表においてKHCO3および/またはHa
HCO3100重量部に対する他の薬剤の配合は次のご
とくである。In addition, the chemicals listed in the table below were dissolved in water to make 100C and this was used as Solution B. Table 1 shows the results of mixing equal volumes of liquids A and B and measuring the gelation temperature, gelation status, and gel time. In addition, a mixture of equal volumes of liquids A and B was prepared at 15°C.
The volume and unconfined compressive strength of the small mogels after being left overnight are shown in Table 2. '1': Table 1 Note: In Table 1, KHCO3 and/or Ha
The composition of other chemicals with respect to 100 parts by weight of HCO3 is as follows.
第 2 表
※ゲル化直後の体積を100%とし一夜後収縮した体積
を示す。Table 2 *The volume immediately after gelation is taken as 100%, and the volume shrunk after overnight is shown.
次ニAI 100m#に:対し/KHCO36g、 1
IaHQ)s 2g、rbsO42g、クエン酸ソー
ダ2gを水に溶解して 100■CとしたB液およびK
HQ]3 6g。Next AI 100m#: vs./KHCO36g, 1
Solution B and K were prepared by dissolving 2g of IaHQ)s, 42g of rbsO, and 2g of sodium citrate in water to make 100■C.
HQ] 3 6g.
HaHC032gを水に溶NLT 100mL!:Lり
B −液をつくり、AB両液またはAB−両液を、つき
固めた豊浦標準砂soo gにそれぞれ混合浸透させて
サンドゲルを作製した。これを水中および大気中(乾燥
しない処置を行う)にて養生し定温20℃にて−軸圧縮
強度の経時変化を測定した。その結果を第2図に示す(
圧縮速さは1%/分)。第2図においてAB−両液によ
るサンドゲルは水中養生の場合、7日後に端面成形でき
ず強度測定が不能となった。Dissolve 32g of HaHC in water and 100mL of NLT! :Liquid B-solution was prepared, and both AB solutions or AB-solutions were mixed and infiltrated into compacted Toyoura standard sand soog to prepare a sand gel. This was cured in water and in the air (without drying), and the change in -axial compressive strength over time was measured at a constant temperature of 20°C. The results are shown in Figure 2 (
Compression speed is 1%/min). In FIG. 2, when the sand gel using AB-both liquids was cured in water, the end face could not be formed after 7 days, making it impossible to measure the strength.
第2図よりAB”両液による比較例はAB両液による実
施例に比べ初期強度が轟くかつ水中強度の低下が著しく
少ないことがわかる。From FIG. 2, it can be seen that the comparative example using both AB'' liquids has a higher initial strength and the decrease in underwater strength is significantly smaller than the Example using both AB liquids.
第1図は本発明に使用されるゲル化剤の組成を示す図で
あり、第2図は本発明の実施例、比較例において水中養
生強度および大気養生強度の変化を示す図である。
第2図中台測定点の記号は以下の通りである。
○ : AB両液使用サンドゲルの大気養生・ :
同 水中養生Δ : AB−両液使
用サンドゲルの大気養生ム : 同
水中!1出願人 大阪曹達株式会社
代理人 弁理士 門多 透FIG. 1 is a diagram showing the composition of the gelling agent used in the present invention, and FIG. 2 is a diagram showing changes in underwater curing strength and air curing strength in Examples and Comparative Examples of the present invention. The symbols for the middle platform measurement points in Figure 2 are as follows. ○: Atmospheric curing of sand gel using both A and B liquids:
Same water curing Δ: AB-atmospheric curing of sand gel using both liquids: Same
Underwater! 1 Applicant Osaka Soda Co., Ltd. Agent Patent Attorney Toru Monda
Claims (1)
剤として重炭酸ソーダおよび/または重炭酸力り 10
0重量部に対しマグネシウムの硫酸塩、塩化物の翠独ま
たは混合物(無水物換算) 5〜10051量部、クエ
ン酸のソーダ塩、カリウム塩の単独または混合物3〜2
00重量部よりなる成分60〜350g/l含む薬液と
を土壌に注入し、硬化させることを特徴とする土質安定
化方法。Sodium silicate solution with a solid content of 10 to 40% by weight and sodium bicarbonate and/or bicarbonate strength as a gelling agent 10
5 to 10051 parts by weight of magnesium sulfate or chloride or a mixture (calculated as anhydride) per 0 parts by weight, 3 to 2 parts of sodium citric acid or potassium salt alone or as a mixture
A method for stabilizing soil quality, which comprises injecting a chemical solution containing 60 to 350 g/l of a component consisting of 0.00 parts by weight into soil and hardening it.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5928382A JPS58174489A (en) | 1982-04-08 | 1982-04-08 | Stabilization method of soil |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5928382A JPS58174489A (en) | 1982-04-08 | 1982-04-08 | Stabilization method of soil |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58174489A true JPS58174489A (en) | 1983-10-13 |
JPS6220238B2 JPS6220238B2 (en) | 1987-05-06 |
Family
ID=13108905
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5928382A Granted JPS58174489A (en) | 1982-04-08 | 1982-04-08 | Stabilization method of soil |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58174489A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008144017A (en) * | 2006-12-08 | 2008-06-26 | Denki Kagaku Kogyo Kk | Ground-grouting agent and ground-grouting method using the same |
JP2009174171A (en) * | 2008-01-23 | 2009-08-06 | Kajima Corp | Water cut-off grout method and water cut-off grout system under high hydraulic pressure |
-
1982
- 1982-04-08 JP JP5928382A patent/JPS58174489A/en active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008144017A (en) * | 2006-12-08 | 2008-06-26 | Denki Kagaku Kogyo Kk | Ground-grouting agent and ground-grouting method using the same |
JP2009174171A (en) * | 2008-01-23 | 2009-08-06 | Kajima Corp | Water cut-off grout method and water cut-off grout system under high hydraulic pressure |
Also Published As
Publication number | Publication date |
---|---|
JPS6220238B2 (en) | 1987-05-06 |
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