JPH04293994A - Soil conditioner - Google Patents
Soil conditionerInfo
- Publication number
- JPH04293994A JPH04293994A JP6049491A JP6049491A JPH04293994A JP H04293994 A JPH04293994 A JP H04293994A JP 6049491 A JP6049491 A JP 6049491A JP 6049491 A JP6049491 A JP 6049491A JP H04293994 A JPH04293994 A JP H04293994A
- Authority
- JP
- Japan
- Prior art keywords
- white carbon
- sodium hydroxide
- hydrated
- fine powder
- silicic acid
- 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
- 239000003516 soil conditioner Substances 0.000 title abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims abstract description 45
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 21
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims abstract description 12
- 239000000843 powder Substances 0.000 claims abstract description 11
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000000292 calcium oxide Substances 0.000 claims abstract description 6
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 11
- 239000000378 calcium silicate Substances 0.000 claims description 10
- 229910052918 calcium silicate Inorganic materials 0.000 claims description 10
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 claims description 10
- 235000012239 silicon dioxide Nutrition 0.000 claims description 10
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims description 9
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 3
- 239000002689 soil Substances 0.000 claims description 3
- 239000011521 glass Substances 0.000 claims description 2
- 239000002075 main ingredient Substances 0.000 claims description 2
- 239000000463 material Substances 0.000 abstract description 5
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract description 4
- 239000011575 calcium Substances 0.000 abstract description 4
- 229910052791 calcium Inorganic materials 0.000 abstract description 4
- 230000035515 penetration Effects 0.000 abstract description 2
- 230000007774 longterm Effects 0.000 abstract 1
- 239000002893 slag Substances 0.000 description 21
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 14
- 239000002245 particle Substances 0.000 description 13
- 235000019353 potassium silicate Nutrition 0.000 description 13
- 230000035699 permeability Effects 0.000 description 10
- 239000000243 solution Substances 0.000 description 9
- 239000003513 alkali Substances 0.000 description 5
- 238000002347 injection Methods 0.000 description 5
- 239000007924 injection Substances 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 239000011440 grout Substances 0.000 description 4
- 239000012670 alkaline solution Substances 0.000 description 3
- 239000004568 cement Substances 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- -1 Ca2+ ions Chemical class 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 238000004220 aggregation Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000001879 gelation Methods 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000011398 Portland cement Substances 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 230000029058 respiratory gaseous exchange Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 229910001845 yogo sapphire Inorganic materials 0.000 description 1
Landscapes
- Consolidation Of Soil By Introduction Of Solidifying Substances Into Soil (AREA)
- Soil Conditioners And Soil-Stabilizing Materials (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、グラウト注入用などの
地盤の改良剤に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a soil improving agent for use in grouting, etc.
【0002】0002
【従来の技術】地盤の改良のためのグラウト注入剤とし
ては、種々のものが従来から用いられてきた。現在の多
くは、水ガラス系またはセメント系のものが大半である
。BACKGROUND OF THE INVENTION Various types of grouting agents have been used for soil improvement. Most of the current materials are water glass-based or cement-based.
【0003】我が国のグラウト剤の歴史を振り返ってみ
れば、1960年代に樋口氏がセメント懸濁液と希釈水
ガラス溶液とを組み合わせたゲルタイムの短い不安定水
ガラスグラウト(LW)、その後このLWに改良を加え
て、微粒子の高炉コロイドセメントと低モル比の水ガラ
ス希釈溶液とを組み合わせた、ゲルタイムが十数分の高
強度で恒久性の高い不安定水ガラスグラウト(C−LW
)、さらに高炉水砕スラグとポルトランドセメントの混
合比率を変化させ各モル比の水ガラス希釈溶液とを組み
合わせた比較的にゲルタイムの長いグラウト(MS)が
基礎になっている。Looking back at the history of grouting agents in Japan, in the 1960s, Mr. Higuchi developed an unstable water glass grout (LW) with a short gel time, which was a combination of a cement suspension and a diluted water glass solution. With improvements, we have developed an unstable water glass grout (C-LW) with high strength and high durability, which has a gel time of more than 10 minutes, by combining fine particles of blast furnace colloidal cement and a water glass diluted solution with a low molar ratio.
), and is based on grout (MS) with a relatively long gel time, which is made by changing the mixing ratio of granulated blast furnace slag and Portland cement and combining water glass diluted solutions with various molar ratios.
【0004】現在では、浸透を目的とした場合には、水
ガラスと硬化剤とを組み合わせた溶液型のものが多い。At present, for the purpose of penetration, there are many solution-type products that combine water glass and a hardening agent.
【0005】しかし、懸濁液型または半懸濁液型のもの
も、高い強度を得るためには、有効であるために、多く
用いられている。However, suspension type or semi-suspension types are also widely used because they are effective in obtaining high strength.
【0006】[0006]
【発明が解決しようとする課題】高炉水砕スラグなどの
カルシウムを含む化合物に対してアルカリを添加すると
、加水分解が生じて高炉水砕スラグの潜在水硬性が発現
する。しかし、この場合、スラグ粒子はアルカリの溶液
と接触すると、スラグ中のSiO2、Al2O3 が溶
出し、次にCa2+イオンが溶出し、これにより、スラ
グ粒子表面にケイ酸カルシウム水和物が生成し、スラグ
粒子相互を凝集結合させる。この凝集の結果、早期に強
度が発現し、長時間経過後の強度たとえば28日強度が
充分でない。
また、保管時または工事の中断時において凝集が進行す
ると、浸透性が悪くなる。[Problems to be Solved by the Invention] When an alkali is added to a calcium-containing compound such as granulated blast furnace slag, hydrolysis occurs and the granulated blast furnace slag develops latent hydraulic properties. However, in this case, when the slag particles come into contact with an alkaline solution, SiO2 and Al2O3 in the slag are eluted, and then Ca2+ ions are eluted, thereby producing calcium silicate hydrate on the surface of the slag particles. The slag particles are coagulated and bonded to each other. As a result of this aggregation, strength develops early, and the strength after a long period of time, for example, after 28 days, is not sufficient. Furthermore, if aggregation progresses during storage or during construction interruptions, permeability will deteriorate.
【0007】したがって、本発明の課題は、高炉水砕ス
ラグなどのカルシウム含有物の優れた水硬性を利用する
とともに、浸透性および長時間経過後の強度に優れた地
盤改良剤を得ることにある。Therefore, an object of the present invention is to utilize the excellent hydraulic properties of calcium-containing materials such as granulated blast furnace slag, and to obtain a ground improvement agent that has excellent permeability and strength after a long period of time. .
【0008】[0008]
【課題を解決するための手段】上記課題は、酸化カルシ
ウムの含有量が20〜50重量%であり、内部構造の9
0%以上がガラス質であり、ブレーン値が5000cm
2 /g以上の微粉末と、水酸化ナトリウムまたは水酸
化カリウムと、BET 表面積が40m2/g以上のホ
ワイトカーボンとを主剤とすることで解決できる。[Means for solving the problem] The above problem is such that the content of calcium oxide is 20 to 50% by weight, and the internal structure is 9%.
0% or more is glassy and Blaine value is 5000cm
This problem can be solved by using as main ingredients a fine powder of 2/g or more, sodium hydroxide or potassium hydroxide, and white carbon with a BET surface area of 40 m2/g or more.
【0009】ホワイトカーボンとしては、無水ケイ酸、
含水ケイ酸、含水ケイ酸カルシウム、含水ケイ酸アルミ
ニウムの群から選ばれた一種または二種以上のものを用
いることができる。[0009] Examples of white carbon include silicic anhydride,
One or more selected from the group of hydrated silicic acid, hydrated calcium silicate, and hydrated aluminum silicate can be used.
【0010】配合量としては、微粉末が200 〜50
0 kg/m3 、10%濃度基準で水酸化ナトリウム
が200 〜500 リットル/m3 、ホワイトカー
ボンが10%水酸化ナトリウム溶液に対して0.01〜
1.0 容積%が好ましい。[0010] The blending amount is 200 to 50% fine powder.
0 kg/m3, sodium hydroxide 200 to 500 liters/m3 based on 10% concentration, white carbon 0.01 to 10% sodium hydroxide solution
1.0% by volume is preferred.
【0011】[0011]
【作用】本発明に従って、微粒ホワイトカーボンを添加
すると、図1に示すように、スラグ粒子間に挟まれるよ
うになる。しかるに、このホワイトカーボン微粒子は、
アルカリ溶液、たとえば水酸化ナトリウム溶液により徐
々に溶解され、その粒子表面にケイ酸ナトリウムを生成
させる。これが、スラグ粒子間を弱く結合させる。この
状態で固化したとしても、図2に示すように、外力たと
えば攪拌力を与えると、結合が弱いために、スラグ粒子
相互は分離離脱し、懸濁液を再流動化させることができ
る。したがって、保管に際して支障がなくなる。[Operation] When fine white carbon is added according to the present invention, it becomes sandwiched between slag particles as shown in FIG. However, these white carbon particles are
It is gradually dissolved in an alkaline solution, such as a sodium hydroxide solution, to form sodium silicate on the particle surface. This creates a weak bond between the slag particles. Even if the slag particles solidify in this state, as shown in FIG. 2, if an external force such as a stirring force is applied, the slag particles will separate from each other due to their weak bond and the suspension can be re-fluidized. Therefore, there is no problem during storage.
【0012】しからば、微粉末ホワイトカーボンに代え
て、希薄な水ガラス溶液を用いることもできると推測で
きるが、実際は、各スラグ粒子表面に水ガラス分子が結
合し、スラグ粒子の全表面が水ガラス分子により被覆さ
れ、ゲル化が早まる。また、再流動化した後の復元性が
悪く、ブリージングが大きくなる。これに対して、ホワ
イトカーボン微粒子は、かかる問題は一切ない。[0012] From this, it can be assumed that a dilute water glass solution can be used in place of the fine powder white carbon, but in reality, water glass molecules bond to the surface of each slag particle, and the entire surface of the slag particle is Covered by water glass molecules, which accelerates gelation. In addition, the restorability after refluidization is poor and breathing becomes large. On the other hand, white carbon fine particles have no such problem.
【0013】[0013]
【実施例】以下本発明を具体的にさらに詳説する。本発
明では、酸化カルシウムの含有量が20〜50重量%で
あり、内部構造の90%以上がガラス質であり、ブレー
ン値が5000cm2 /g以上の微粉末を用いる。EXAMPLES The present invention will be specifically explained in further detail below. In the present invention, a fine powder with a calcium oxide content of 20 to 50% by weight, an internal structure of 90% or more of glass, and a Blaine value of 5000 cm2/g or more is used.
【0014】この代表例としては、高炉水砕スラグの微
粉末を挙げることができる。他の冶金スラグも用いるこ
とができる。酸化カルシウムの含有量はより好ましくは
25〜35重量%である。ブレーン値はとしては、浸透
性の点でより好ましくは8000〜16000cm2
/g である。粗大な粒子の場合、地盤中に対する浸透
性が悪い。ブレーン値がより高くとも、浸透性の向上は
さほど期待できず、また粉砕に要するコストの増大を招
く。A representative example of this is fine powder of granulated blast furnace slag. Other metallurgical slags can also be used. The content of calcium oxide is more preferably 25 to 35% by weight. The Blaine value is more preferably 8,000 to 16,000 cm2 in terms of permeability.
/g. Coarse particles have poor permeability into the ground. Even if the Blaine value is higher, no significant improvement in permeability can be expected, and the cost required for pulverization increases.
【0015】この種のスラグに対して、アルカリが添加
される。アルカリとしては、水酸化ナトリウムが好適で
あるが、水酸化カリウムもコストの点を除けば使用でき
るとともに、効果は基本的に同一であることを確認済で
ある。さらに、本発明においては、微粒ホワイトカーボ
ンが添加される。この微粒ホワイトカーボンとしては、
無水ケイ酸、含水ケイ酸、含水ケイ酸カルシウム、含水
ケイ酸アルミニウムの群から選ばれた一種または二種以
上のものを用いることができる。BET 表面積として
は、40m2/g以上、好ましくは50〜300m2/
gのものを好適に用いることができる。とりわけ、含水
ケイ酸カルシウムは、アルカリ溶液によるスラグ粒子の
加水分解速度を遅延させるので、ゲルタイムの調整が容
易となり、望ましい。[0015] Alkali is added to this type of slag. As the alkali, sodium hydroxide is preferred, but potassium hydroxide can also be used except for cost, and it has been confirmed that the effects are basically the same. Furthermore, in the present invention, fine white carbon is added. As this fine white carbon,
One or more selected from the group of anhydrous silicic acid, hydrated silicic acid, hydrated calcium silicate, and hydrated aluminum silicate can be used. The BET surface area is 40 m2/g or more, preferably 50 to 300 m2/g.
g can be suitably used. In particular, hydrated calcium silicate is desirable because it delays the rate of hydrolysis of slag particles by an alkaline solution, making it easier to adjust the gel time.
【0016】本発明に係る地盤改良剤の好適な配合は、
酸化カルシウム含有微粉末が200 〜500 kg/
m3 、10%濃度基準で水酸化ナトリウムが200
〜500 リットル/m3 、ホワイトカーボンが10
%水酸化ナトリウム溶液に対して0.01〜1.0 容
積%である。微粉末は、少量のアルカリによっても硬化
反応を生じるが、強度の早期発現の点で200 リット
ル/m3 以上含有するのが好ましい。逆に、水酸化ナ
トリウムが過剰であると、地盤中にアルカリが残存し、
生活環境を阻害する要因を発生させる虞れがある。水酸
化ナトリウムの濃度によって、添加量は一次反比例的に
調節できる。たとえば、5%濃度の場合には、400
〜1000リットル/m3 となる。ホワイトカーボン
微粒子の添加量は、効果を発現させるために、0.01
容積%以上添加することが要求される。逆に、過度に添
加量が多いと、ゲルタイムが短くなるとともに、浸透性
を阻害する。[0016] A preferred formulation of the ground improvement agent according to the present invention is as follows:
200 to 500 kg of calcium oxide-containing fine powder
m3, sodium hydroxide is 200% based on 10% concentration.
~500 liters/m3, white carbon 10
% sodium hydroxide solution. Although a small amount of alkali causes a hardening reaction, the fine powder is preferably contained in an amount of 200 liters/m 3 or more for early development of strength. Conversely, if sodium hydroxide is excessive, alkali will remain in the ground,
There is a risk of causing factors that impede the living environment. Depending on the concentration of sodium hydroxide, the amount added can be adjusted in linear inverse proportion. For example, for a 5% concentration, 400
~1000 liters/m3. The amount of white carbon fine particles added is 0.01 to achieve the effect.
It is required to add more than % by volume. On the other hand, if the amount added is too large, the gel time will be shortened and the permeability will be inhibited.
【0017】本発明の係る地盤改良剤は、通常、各材料
を予め調合し一液で対象地盤の施す、たとえば注入管を
介して地盤中に注入することができるが、酸化カルシウ
ム含有微粉末の懸濁液と水酸化ナトリウム溶液とを別に
注入管に送給し、注入管内でまたは地盤中で合流混合さ
せることができる。この場合、ホワイトカーボンは一方
の液側に添加することができる。さらに、本発明に係る
地盤改良剤は、グラウト注入の場合のほか、攪拌混合工
法などの他の工法にも用いることができる。The ground improvement agent according to the present invention can be applied to the target ground as a single solution by preparing each material in advance, for example, by injecting it into the ground through an injection pipe. The suspension and the sodium hydroxide solution can be fed separately into the injection tube and mixed together in the injection tube or in the ground. In this case, white carbon can be added to one liquid side. Furthermore, the ground improvement agent according to the present invention can be used not only for grout injection but also for other construction methods such as stirring and mixing construction methods.
【0018】〔実施例〕以下に実施例を示し本発明の効
果を明らかにする。
(実施例1)高炉水砕スラグの微粉末(ブレーン値15
000cm2 /g)の350kg/m3 に対して1
0%濃度の水酸化ナトリウムを350リットル/m3
を添加する配合の下で、含水ケイ酸、含水ケイ酸カルシ
ウムおよび希釈水ガラスを添加し、粘性の変化を調べた
。結果を表1に示す。添加量は体積%である。[Example] Examples are shown below to clarify the effects of the present invention. (Example 1) Fine powder of granulated blast furnace slag (Blaine value 15
1 for 350kg/m3 of 000cm2/g)
350 liters/m3 of 0% sodium hydroxide
Hydrous silicic acid, hydrated calcium silicate, and diluted water glass were added to examine changes in viscosity. The results are shown in Table 1. The amount added is % by volume.
【0019】[0019]
【表1】[Table 1]
【0020】この結果から、希釈水ガラスを添加した場
合より、含水ケイ酸および含水ケイ酸カルシウムを添加
する場合の方が、粘度の上昇を抑制でき、かつ含水ケイ
酸カルシウムはその効果が大きいことが判った。また、
1.0 体積%以上となると、ゲル化時間が短くなり、
好ましくないことも判った。
(実施例2)さらに、含水ケイ酸、含水ケイ酸カルシウ
ムおよび希釈水ガラスを添加した各添加量配合において
、練り置き時間を10分に設定し、注入管により豊浦標
準砂を充填したモールド(直径5mmΦ×長さ100
mm)に対して、注入圧力1kg/cm2 で一液注入
を行い、その浸透性および28日後の強度を調べた結果
を、表2に示した。この結果から、ホワイトカーボンの
添加は浸透性および強度の向上をもたらし、かつ含水ケ
イ酸カルシウムは含水ケイ酸より、浸透性が良好となる
ことが判明した。[0020] From this result, it is found that the increase in viscosity can be suppressed more when adding hydrated silicic acid and hydrated calcium silicate than when diluted water glass is added, and hydrated calcium silicate has a greater effect. It turns out. Also,
When the content is 1.0% by volume or more, the gelation time becomes shorter;
I also found that I didn't like it. (Example 2) Furthermore, in each addition amount combination of hydrated silicic acid, hydrated calcium silicate, and diluted water glass, the kneading time was set to 10 minutes, and a mold (diameter 5mmΦ×Length 100
Table 2 shows the results of investigating the permeability and strength after 28 days by injecting a single liquid into the sample (mm) at an injection pressure of 1 kg/cm2. These results revealed that the addition of white carbon improved permeability and strength, and that hydrated calcium silicate had better permeability than hydrated silicic acid.
【0021】[0021]
【表2】[Table 2]
【0022】[0022]
【発明の効果】以上の通り、本発明によれば、高炉水砕
スラグなどのカルシウム含有物の優れた水硬性を利用で
きるとともに、浸透性および長時間経過後の強度に優れ
た地盤改良剤を得ることができる。As described above, according to the present invention, it is possible to utilize the excellent hydraulic properties of calcium-containing substances such as granulated blast furnace slag, and also to create a ground improvement agent that has excellent permeability and strength after a long period of time. Obtainable.
【図1】高炉水砕スラグ粒子に対するホワイトカーボン
の添加による反応機構の説明図である。FIG. 1 is an explanatory diagram of the reaction mechanism due to the addition of white carbon to granulated blast furnace slag particles.
Claims (3)
%であり、内部構造の90%以上がガラス質であり、ブ
レーン値が5000cm2 /g以上の微粉末と、水酸
化ナトリウムまたは水酸化カリウムと、BET 表面積
が40m2/g以上のホワイトカーボンとを主剤とする
ことを特徴とする地盤改良剤。Claim 1: A fine powder having a calcium oxide content of 20 to 50% by weight, an internal structure of 90% or more of glass, and a Blaine value of 5000 cm2/g or more, and sodium hydroxide or potassium hydroxide. and white carbon having a BET surface area of 40 m2/g or more as main ingredients.
イ酸、含水ケイ酸カルシウム、含水ケイ酸アルミニウム
の群から選ばれた一種または二種以上のものである請求
項1記載の地盤改良剤。2. The ground improvement agent according to claim 1, wherein the white carbon is one or more selected from the group consisting of anhydrous silicic acid, hydrated silicic acid, hydrated calcium silicate, and hydrated aluminum silicate.
、10%濃度基準で水酸化ナトリウムが200 〜50
0 リットル/m3 、ホワイトカーボンが10%水酸
化ナトリウム溶液に対して0.01〜1.0 容積%で
ある請求項1記載の地盤改良剤。Claim 3: Fine powder is 200 to 500 kg/m3
, sodium hydroxide is 200 to 50 on a 10% concentration basis.
2. The soil improvement agent according to claim 1, wherein the white carbon is 0.01 to 1.0% by volume based on the 10% sodium hydroxide solution.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6049491A JP2860718B2 (en) | 1991-03-25 | 1991-03-25 | Ground improvement agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6049491A JP2860718B2 (en) | 1991-03-25 | 1991-03-25 | Ground improvement agent |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04293994A true JPH04293994A (en) | 1992-10-19 |
JP2860718B2 JP2860718B2 (en) | 1999-02-24 |
Family
ID=13143906
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6049491A Expired - Fee Related JP2860718B2 (en) | 1991-03-25 | 1991-03-25 | Ground improvement agent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2860718B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5531234B1 (en) * | 2013-02-08 | 2014-06-25 | 強化土株式会社 | Ground injection material and ground injection method |
-
1991
- 1991-03-25 JP JP6049491A patent/JP2860718B2/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5531234B1 (en) * | 2013-02-08 | 2014-06-25 | 強化土株式会社 | Ground injection material and ground injection method |
Also Published As
Publication number | Publication date |
---|---|
JP2860718B2 (en) | 1999-02-24 |
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