JPS6023475A - Soil-hardening agent - Google Patents

Soil-hardening agent

Info

Publication number
JPS6023475A
JPS6023475A JP12949283A JP12949283A JPS6023475A JP S6023475 A JPS6023475 A JP S6023475A JP 12949283 A JP12949283 A JP 12949283A JP 12949283 A JP12949283 A JP 12949283A JP S6023475 A JPS6023475 A JP S6023475A
Authority
JP
Japan
Prior art keywords
soil
cement
complex compound
chloride
cobalt chloride
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.)
Pending
Application number
JP12949283A
Other languages
Japanese (ja)
Inventor
Hiroshi Okazaki
岡崎 弘
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.)
DAIWA SEKIYU KK
Original Assignee
DAIWA SEKIYU KK
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 DAIWA SEKIYU KK filed Critical DAIWA SEKIYU KK
Priority to JP12949283A priority Critical patent/JPS6023475A/en
Publication of JPS6023475A publication Critical patent/JPS6023475A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To provide the titled soil-hardening agent which is an alkaline mixture obtained by adding less than specific amount of a cobalt chloride complex compound to an aqueous solution of an alkali metal salt, and gives a hardened soil having excellent strength and elastic modulus and resistant to cracking when used in combination with cement. CONSTITUTION:The objective agent is a mixture having alkaline nature (preferably 9-12pH) and obtained by adding <=4(wt)%, preferably 0.1-0.5% cobalt chloride complex compound (preferably a cobalt chloride ammine complex compound produced by the reaction of ammonium chloride, an alkali metal carbonate, cobalt chloride and oxygen) to an aqueous solution of an alkali metal salt (preferably a combination of sodium carbonate, potassium carbonate and sodium chloride).

Description

【発明の詳細な説明】 本発明は土壌硬化処理剤に関する。[Detailed description of the invention] The present invention relates to a soil hardening agent.

従来土壌硬化剤としては多くの特許、文献が発表されて
いるが、注入方式をとった珪酸ソーダ(水力ラス)を主
としたものが多く、薬剤使用による混合その他の方式に
よる土壌硬化の特許は比較的少ない。土壌処理を行う場
合薬液には自体硬化又は固結能力がないので当然固結剤
として取扱いやすく且つ高強度のセメントを併用する事
が考えられる。特許833570号もその一例と云える
。即ちこの特許は土壌をセメントとで硬化する場合アル
カリ金属塩、アルカリ土類金属塩の水溶液にアンモニウ
ム塩を融合(添加すると言う意味か)する事を特徴とし
ている。実施例をみても塩化アルミニウム、塩化−第二
鉄等強酸性塩が用いられ、事実実施例1の混合液は25
°Cに於て木発明者が処方に従い調製し、測定した場所
PH4,0、実施例2はpH1,8であった。又塩化ア
ンモニウムも全液中10〜15重量%と可成り多量に使
用されている。之の正否は別として本発明者は荀くも3
 CaO・ SiO□(珪酸3石灰)を主とするセメン
の水和→凝結→硬化という正常硬化過程が水利時発生す
る多量のCa(OH)2 (水酸化カルシウム)により
強度のアルカリ性で進行する事により最終経時硬化強度
を示す事実から、急結性のためかかる強酸性溶液を添加
する事はセメントの正常硬化に好ましい筈はなく、多く
の塩化物を添加する事は土壌はともあれセメントに対し
ては複分解により多量のCa1l 2(塩化カルシウム
)の生成を来し可溶化物質であるため硬化後好ましから
ざる事は勿論、又セメン1・の硬化後の強度はセメント
ゲルの微細結晶が大きい表面エネルギーで互いに凝集交
錯して緻密な網状構造が出来、結合が強化され硬化が進
んで強度か発現する。その際セメント水利生成物は20
0rn’/Hにも及ぶ大きい比表面積をもった微細粒子
で之が相接近して存在するため分子間引力が大きく働き
更にこの力の10倍も強い水素結合や電荷の不均衡によ
る化学結合力が加わって強度を示すものである。かかる
意味からも強酸性混合溶液を加える市は土に重点をおき
すぎる反面、セメントの正常硬化を攪乱し十分な強度は
得られないであろうと推察する。即ち極部的凝集又は凝
固をおこし、このものは瞬間的であるから余計緻密な網
状構造をもった正常硬化とは全く逆な結果となる。本発
明は以上の事実から一方に偏せざるよう土壌は勿論、固
結硬化の最大の鍵をにぎるセメントの正常硬化過程に相
応させるべく混合薬剤は常にアルカリ側を保持するよう
調整した本が大きな特徴である。本発明の機構解析を行
う前に本発明に適合する薬剤の種類をのべる。
Many patents and documents have been published regarding conventional soil hardening agents, but most of them are based on sodium silicate (hydraulic lath), which uses an injection method, and there are no patents on soil hardening using mixing or other methods using chemicals. Relatively few. When performing soil treatment, since chemical solutions do not have the ability to harden or solidify by themselves, it is natural to consider using cement, which is easy to handle and has high strength, as a solidifying agent. Patent No. 833570 can also be said to be an example. That is, this patent is characterized in that when hardening soil with cement, ammonium salts are fused (or added) to an aqueous solution of alkali metal salts and alkaline earth metal salts. Looking at the examples, strong acid salts such as aluminum chloride and ferric chloride were used, and in fact, the mixed solution of Example 1 was 25
°C according to the recipe prepared by the inventor and measured at a site where the pH was 4.0, and in Example 2 the pH was 1.8. Further, ammonium chloride is also used in a fairly large amount of 10 to 15% by weight in the total liquid. Regardless of whether this is true or not, the inventor is Xun Kumo 3
The normal hardening process of hydration → setting → hardening of cement, which is mainly composed of CaO・SiO□ (tricalcium silicate), progresses in strong alkalinity due to the large amount of Ca(OH)2 (calcium hydroxide) generated during irrigation. From the fact that shows the final hardening strength over time, adding such a strong acidic solution is not favorable for the normal hardening of cement due to its rapid setting, and adding a large amount of chloride is not good for cement, let alone soil. Of course, Cement 1 produces a large amount of Ca1l2 (calcium chloride) through double decomposition, which is not desirable after hardening because it is a solubilized substance.Also, the strength of Cement 1 after hardening is due to the large surface energy of the fine crystals of cement gel. They coagulate and intertwine with each other to form a dense network structure, which strengthens the bonds and progresses in hardening, developing strength. At that time, the cement water use product is 20
Because they are microscopic particles with a large specific surface area of 0rn'/H, the intermolecular attraction is strong because they exist in close proximity to each other, and the chemical bonding force due to hydrogen bonding and charge imbalance is ten times stronger than this force. is added to indicate strength. From this perspective, it can be inferred that the city that adds a strongly acidic mixed solution places too much emphasis on the soil, but on the other hand, it disturbs the normal hardening of the cement and may not be able to obtain sufficient strength. That is, local aggregation or coagulation occurs, and since this is instantaneous, the result is completely opposite to normal curing, which has an extremely dense network structure. Based on the above facts, the present invention is a large book in which the mixed chemicals are adjusted to always maintain the alkaline side in order to correspond to the normal hardening process of not only soil but also cement, which holds the biggest key to solidification and hardening. It is a characteristic. Before conducting a mechanistic analysis of the present invention, the types of drugs compatible with the present invention will be described.

アルカリ金属塩としてはカリウム、ナトリウム、リチウ
ム等の炭酸塩、重炭酸塩、塩化物、水酸化物等水可溶性
又は一定溶解度範囲で水に可溶性なる塩類の少なくとも
一種以上であり、之等の単体又は混合物が完全に水溶液
であって、併も4重量%(全液中)以下の塩化コバルト
錯化合物を添加しても常にアルカリ性である必要がある
。木1」的に最も効果のあるものは炭酸ナトリウム、炭
酸カリウムと塩化ナトリウムの組合せである事を確認し
た。勿論上述の他の塩類でも本発明に有効である。又、
アルカリ金属塩水溶液に更に効果を高めるため、又は特
殊の要望に応するためアルカリ性を保持させる本目的を
損わぬ限りアルカリ土類金属塩(水不溶解物も含む)を
添加する事や他の物質を添加する事も一向に差し支えな
い。本発明者は上述のアルカリ金属塩と本発明効果に相
乗作用を与えるため遷移金属元素を検討した所、効果、
安定性、速乾性その他見ての点からみて塩化コ/ヘルド
の錯化合物が最も効果的な事を発見した。塩化ナトリウ
ム、炭酸ソーダ、炭酸カリの混合水溶液に塩化アンモニ
ウム丈を入れたものは本発明目的のためには硬化時間が
余りにも早すぎ、J」つ硬化物はもろい欠点があり、塩
化コバルトを加え錯化合物にしたものは硬化時間が適当
な範囲に入り且つもろさが全くみられない強度の高い硬
化物をつくる。又逆に塩化アンモニウムをぬいてjn化
コバルト丈を添加したものは液相分離を瞬間的におこし
、性能的に本目的を満足せず之に塩化アンモニウムを加
えると安定な水溶液となり木目的に合致する事を知った
The alkali metal salts include at least one kind of salts such as carbonates, bicarbonates, chlorides, and hydroxides such as potassium, sodium, and lithium, which are soluble in water or are soluble in water within a certain solubility range, and these salts may be used singly or The mixture must be a completely aqueous solution and must always remain alkaline even if less than 4% by weight (based on the total liquid) of the cobalt chloride complex compound is added. It was confirmed that the most effective combination of sodium carbonate, potassium carbonate and sodium chloride was found to be most effective. Of course, other salts mentioned above are also effective in the present invention. or,
In order to further enhance the effect of the alkali metal salt aqueous solution or to meet special needs, alkaline earth metal salts (including water-insoluble substances) may be added or other additives may be added as long as the main purpose of maintaining alkalinity is not impaired. There is no problem with adding substances. The present inventor investigated transition metal elements to have a synergistic effect with the above-mentioned alkali metal salts and the effects of the present invention, and found that the effects,
It has been discovered that a complex compound of cochloride/Held is the most effective in terms of stability, quick drying, and other aspects. A mixed aqueous solution of sodium chloride, soda carbonate, and potassium carbonate containing ammonium chloride cures too quickly for the purpose of the present invention, and the cured product has the disadvantage of being brittle. When made into a complex compound, the curing time falls within an appropriate range and a highly strong cured product with no brittleness is produced. On the other hand, when ammonium chloride is removed and cobalt chloride is added, liquid phase separation occurs instantaneously, which does not satisfy the intended purpose in terms of performance, but when ammonium chloride is added, a stable aqueous solution is created, which meets the wood's purpose. I learned what to do.

本発明に於て発明者は各種実験の結果安定性、硬化速度
、強度又経済的面その他から塩化コバルト錯化合物は全
液中4重量%以下が適当で、好ましくは、0.1〜0.
5重量%であり、4重量%をこえると強度上昇、硬化速
度が添加に値する程の効果はみられずかつ不経済となる
。本発明に係わる塩化コへルト錯化合物は塩化アンモニ
ウム、アルカリ金属炭酸塩、塩化コバルト及び酸素との
反応により生成する塩化コバルトアンミン錯化合物と思
われるが、この場合錯化合物に必要な塩化アンモニウム
の量は理論的には錯化合物と同量であるが、一方にはセ
メントO水和反応時に発生する水酸化カルシウムとの反
応に消費される事も十分考えられるので理論量より多口
に添加する必要はあるが、過大にすぎると前述の如く水
酸化力リシウムとの反応により水可溶性の好ましからざ
る塩化カルシウムを多量に生成するので、少なくも4昆
合初期に於て塩化コバルト錯化合物を最優先的に形成さ
せる事が要点であるため塩化アンモニウムは理論量の2
.5倍あたりが適当と思われる。従って前述の最適範囲
に於て使用される塩化アンモニウムは0.3〜1.5重
量%となり添加量につし1ても冒頭に上げた特許の実施
例2種類と比較しても該特許が全液中10〜15重量%
使用しているのに比較すれば本発明の場合の塩化アンモ
ニウム使用量が余りにも僅少であり、且つ本発明は溶液
pHが凡て7以上で、好ましくは 9〜12を示すのに
対し該特許の溶液pHは4.0〜1.5の強酸性を示し
て居り、併も本発明の場合は塩化コバルト錯化合物の存
在意義にその特徴を有する車等から該特許とは全く異な
ったものである事が分る。
As a result of various experiments, the inventor of the present invention found that the amount of the cobalt chloride complex compound in the total solution is 4% by weight or less, preferably 0.1 to 0.0%, based on stability, curing speed, strength, economical aspects, etc.
The amount is 5% by weight, and if it exceeds 4% by weight, the effect of increasing strength and curing speed will not be sufficient to warrant addition, and it will become uneconomical. The coherto chloride complex compound according to the present invention is believed to be a cobalt chloride ammine complex compound produced by a reaction with ammonium chloride, an alkali metal carbonate, cobalt chloride, and oxygen; in this case, the amount of ammonium chloride required for the complex compound is Theoretically, it is the same amount as the complex compound, but it is also quite conceivable that it will be consumed in the reaction with calcium hydroxide generated during the cement O hydration reaction, so it is necessary to add more than the theoretical amount. However, if the amount is too large, a large amount of undesirable water-soluble calcium chloride will be produced due to the reaction with hydroxide lithium as mentioned above, so at least in the early stage of four-combination, the cobalt chloride complex compound should be given top priority. Since it is important to form a
.. Around 5 times seems appropriate. Therefore, the amount of ammonium chloride used in the above-mentioned optimum range is 0.3 to 1.5% by weight. 10-15% by weight in total liquid
The amount of ammonium chloride used in the present invention is too small compared to that used in the present invention, and the solution pH in the present invention is all 7 or more, preferably 9 to 12, whereas the patent The pH of the solution is strongly acidic, ranging from 4.0 to 1.5, and in the case of the present invention, the reason for the existence of a cobalt chloride complex compound is completely different from that of the patent, since cars, etc. have this feature. I understand something.

本発明の水溶液を使用し、セメントと共に土壌を硬化す
る場合骨材、有効」=壌、有機固結剤、硬化促進剤その
他の添加剤を併用する事も木目的に違反せぬ限り一向に
差支えない。塩化コバルト錯化合物の存在下、本発明の
硬化及び満足行く強度の得られる機構については本発明
者は以下の如く推論する。
When using the aqueous solution of the present invention to harden soil together with cement, it is effective to use aggregate, soil, organic consolidation agents, hardening accelerators, and other additives, as long as it does not violate the purpose of the tree. . The present inventor speculates as follows about the mechanism by which the present invention cures and obtains satisfactory strength in the presence of a cobalt chloride complex compound.

成分中の炭酸塩は土壌表面及び内部に含有される有機物
質例えば油脂類は之を除去と同時に水中にO/W型分散
させ、有機酸、ハロゲン等は可溶性化して水に溶解させ
、同時に土壌表面に十分な濡れ性を与えるのに著効を発
揮する。他方本発明の骨子たる塩化コバルト錯化合物は
土壌及びセメントに対し粒子の凝集力を適度に抑制しつ
つ均一に分散を行わせるため、一般にセメント使用の場
合に見られる如きブリージング(水がセメントゲルから
分離する現象)がおこりにくくなり、且つ塩化すI・リ
ウムによりシクントロピー性が助長され分散効果維持に
貢献する。かくて高度均一分散状態でセメント粒子は水
和反応をおこし、分散せる土壌(骨材その他を併用する
場合それらをふくめ)を島とし、セメントベイストが海
構造の役を果す所謂島海構造(Sea−Islands
 5tructure)を形成し、その結果土質粒子の
間隙を均一なセメント水和ペイストで充填し、バインダ
ー(固結剤)として機能するため土質の水密化が著しく
向−1ニする。又、土壌、骨材等に含有されるコロイド
性シリカとセメント中に本来0.5%前後含有されるN
a20(酸化ソータ)、に20 (酸化カリウム)との
間に含有炭酸塩の補助反応と塩化コバルト錯化合物の触
媒作用により土壌、七メント粒子に活性点をおく珪酸ア
ルカリオリゴマー(低重縮合体)を形成し、之がセメン
ト自体の凝結、硬化と並行し存在する塩化ナトリウムに
より凝集反応を始め重縮合が進行し、共有結合により網
状構造をつくりセメント硬化過程物質と一体化するもの
と思われる。島海構造に於てセメント及び珪酸アルカリ
オリゴマーの両者が最後に一体化される。本発明者はこ
の島海構造形成並びにセメン!・自体のjlE常硬化反
応と別途に無機オリゴマーを形成させる点に塩化コバル
ト錯化合物は大きい貢献を果しているものと推定する。
Carbonates in the ingredients remove organic substances contained on and inside the soil, such as oils and fats, and at the same time disperse them in water in an O/W type, while organic acids, halogens, etc. are solubilized and dissolved in water, and at the same time, they are dissolved in soil. It is extremely effective in providing sufficient wettability to the surface. On the other hand, the cobalt chloride complex compound, which is the mainstay of the present invention, can be uniformly dispersed in soil and cement while appropriately suppressing the cohesive force of particles. (separation phenomenon) is less likely to occur, and sichuntropy is promoted by I.lium chloride, contributing to maintaining the dispersion effect. In this way, the cement particles undergo a hydration reaction in a highly uniformly dispersed state, and the soil to be dispersed (including aggregates and other materials when used together) becomes islands, creating a so-called island-sea structure (Sea) in which the cement bait serves as a sea structure. -Islands
As a result, the gaps between the soil particles are filled with a uniform cement hydration paste, which functions as a binder (consolidating agent), thereby significantly improving the watertightness of the soil. In addition, colloidal silica contained in soil, aggregate, etc. and N, which is originally contained around 0.5% in cement.
Alkali silicate oligomer (low polycondensate) that places active sites in soil and 7-ment particles through the auxiliary reaction of the carbonate contained between A20 (oxidation sorter) and Ni20 (potassium oxide) and the catalytic action of the cobalt chloride complex compound. It is thought that, in parallel with the coagulation and hardening of the cement itself, the presence of sodium chloride causes a coagulation reaction and polycondensation to proceed, creating a network structure through covalent bonds and integrating with the cement hardening process materials. Both the cement and the alkali silicate oligomer are finally integrated in the island-sea structure. The present inventor is involved in the formation of this island-sea structure as well as cement! - It is estimated that the cobalt chloride complex compound makes a large contribution to the formation of inorganic oligomers in addition to the jlE normal curing reaction itself.

なお、有機物質中アミン類は特にこの錯化合物の配位子
として簡単に吸着され、脱臭に寄与し、油脂を始めとす
るセメントとの密着妨害素因は完全に処置され、濡れ状
態も均一となり且つ錯化合物に包囲された吸着界面が極
度にイオン活性状態にある島構造にファンデルワールス
力が始因となり、更にイオン、電気的その他の吸着要因
によりセメント水和ペイスI・の海構造は強力な吸着密
着を行いつつ凝結を経て硬化するに至る。
In addition, amines in organic substances are easily adsorbed especially as ligands of this complex compound, contributing to deodorization, and factors that interfere with adhesion with cement, such as oils and fats, are completely eliminated, and the wet state becomes uniform. The van der Waals force is the origin of the island structure in which the adsorption interface surrounded by complex compounds is in an extremely ionically active state, and the sea structure of cement hydrated Pace I is caused by ionic, electrical and other adsorption factors. While performing adsorption and adhesion, it hardens through condensation.

本発明者は本発明によって得られた固形化物が優れた強
度を保持し、適度の弾性を有し、一点に加えられた衝撃
が一般セメント製品の如く局部破壊をおこして亀裂に発
展するのとことなり衝撃力が拡散するため亀裂破壊がお
こりにくい事を確認して居り、之は網状化の完成及びそ
れがスプリングの役を果し衝翳帯を全体に亘って形成し
ているためと判ぜざるを得ないのである。
The present inventor has found that the solidified product obtained by the present invention maintains excellent strength and has appropriate elasticity, and that an impact applied to one point will not cause local fracture and develop into cracks like in general cement products. It has been confirmed that crack failure is less likely to occur because the impact force is diffused, and this is thought to be due to the completion of the reticulation and the formation of a web that acts as a spring throughout. It is inevitable.

本発明は目的によりセメント量、各薬剤成分の選択組合
せにより固形硬化物は勿論、粒状、顆粒状のものも製造
する事は可能で、原理は全て上述の過程を経過する事は
云う迄もない。
According to the present invention, it is possible to produce solid hardened products as well as granular and granular products by selecting and combining the amount of cement and each chemical component depending on the purpose, and it goes without saying that the principle is to follow the above-mentioned process. .

以」−の如く本発明機構の推論を要約すると、(1)炭
酸アルカリ塩及び塩化コバルト錯化合物の土壌に対する
含有有機物質処理と濡れ性の完全化に伴う表面活性化、
(2)土壌、セメント粒子の均−分散及び塩化ナトリウ
ムによる分散保持性、(3)島海構造の形成及びそれに
伴なう水密化態勢確立、(4)珪酸アルカリオリゴマー
生成と七メント水和物の凝集一体化の上での硬化による
網状重縮合物質の生成完了という事になる。
To summarize the reasoning of the mechanism of the present invention as follows, (1) treatment of the soil with organic substances containing alkali carbonates and cobalt chloride complex compounds and surface activation associated with perfecting wettability;
(2) Uniform dispersion of soil and cement particles and dispersion retention due to sodium chloride, (3) Formation of island-sea structure and establishment of watertight system associated with it, (4) Formation of alkali silicate oligomers and heptament hydrate This means that the formation of a network polycondensate material is completed by curing upon coagulation and integration of the polycondensate.

次に、実施例を示し本発明をさらに詳細に説明する。Next, the present invention will be explained in more detail by showing examples.

実施例1 (試料)関東ローム±(水分35.5%)(処理)関東
ローム」二 (5m/+n篩 4mesh通過)100%ポルトラン
ドセメント 20% 混 合 液 2z (4昆合液処方) 塩化ナトリウム 8.5χ 炭酸カリウム 6.0% 炭酸ナトリウム 7.0% 塩化アンモニウム 1.5% 塩化コバルト 0.3% 水 78.7% 言4 100% 予め土壌とセメントをよく混合した上で、薬液を添加攪
拌混合したものをdia5cm、深さ10c+nの金属
性成型器に3日間放置後説型し、ポリエチレン袋に密閉
常温にて養生、7日間、28日間の経時強度(圧縮強度
)を試料5ケについて測定平均値を下に示す。尚、圧縮
強度はJIS A1211準拠のCBR試験装置により
測定した。
Example 1 (Sample) Kanto loam ± (moisture 35.5%) (Processing) Kanto loam 2 (passed through 5m/+n sieve, 4 mesh) 100% Portland cement 20% Mixed liquid 2z (4 molten liquid formulation) Sodium chloride 8.5χ Potassium carbonate 6.0% Sodium carbonate 7.0% Ammonium chloride 1.5% Cobalt chloride 0.3% Water 78.7% Word 4 100% Mix the soil and cement well beforehand, then add the chemical solution. The stirred mixture was left in a metal molding machine with a diameter of 5 cm and a depth of 10 cm + n for 3 days, then molded, sealed in a polyethylene bag and cured at room temperature, and the strength over time (compressive strength) for 7 and 28 days was measured for 5 samples. The measured average values are shown below. Note that the compressive strength was measured using a CBR testing device based on JIS A1211.

(試料)赤 土(水分40%以下) (処理)赤 土 100X ポルトランドセメント 17% 混 合 液 2,5z (混合液処方) 塩化ナトリウム 6.Oz 塩化カリウム 3.Oz 炭酸すトリウム′8.5% 炭酸カリウム 5.8z 塩化アンモニウム 0.75% 塩化コバルト 0.15% 水 77.8% 計 100% 添添加台は実施例1に回し 試験片はdia5cm深さ10cm円筒形金属性成型機
使川、3日後説型大気中養生放置。
(Sample) Red soil (moisture 40% or less) (Processing) Red soil 100X Portland cement 17% Mixed liquid 2.5z (Mixed liquid formulation) Sodium chloride 6. Oz potassium chloride 3. Oz Thorium carbonate '8.5% Potassium carbonate 5.8z Ammonium chloride 0.75% Cobalt chloride 0.15% Water 77.8% Total 100% The addition table was the same as in Example 1, and the test piece was 5 cm in diameter and 10 cm in depth. Cylindrical metal forming machine Shigawa was left to cure in the atmosphere for 3 days.

最大荷重 4,100kgf (圧縮強度単位kgf/cn+2(’N/mm2.) 
)−に91
Maximum load 4,100kgf (compressive strength unit kgf/cn+2 ('N/mm2.)
)-91

Claims (1)

【特許請求の範囲】[Claims] l)アルカリ金属塩水溶液に4重量%以下の塩化コバル
ト錯化合物を存在せしめ、併も之等の混合液がアルカリ
性であることを特徴とするセメントと共に土壌を処理す
るに当り使用する土壌硬化処理剤。
l) A soil hardening treatment agent used in treating soil with cement, characterized in that 4% by weight or less of a cobalt chloride complex compound is present in an aqueous alkali metal salt solution, and the mixture is alkaline. .
JP12949283A 1983-07-18 1983-07-18 Soil-hardening agent Pending JPS6023475A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12949283A JPS6023475A (en) 1983-07-18 1983-07-18 Soil-hardening agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12949283A JPS6023475A (en) 1983-07-18 1983-07-18 Soil-hardening agent

Publications (1)

Publication Number Publication Date
JPS6023475A true JPS6023475A (en) 1985-02-06

Family

ID=15010813

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12949283A Pending JPS6023475A (en) 1983-07-18 1983-07-18 Soil-hardening agent

Country Status (1)

Country Link
JP (1) JPS6023475A (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5543148A (en) * 1978-09-22 1980-03-26 Kajima Corp Material for solidifying flimsy ground
JPS57202374A (en) * 1981-06-09 1982-12-11 Masao Tamura Soil hardening agent

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5543148A (en) * 1978-09-22 1980-03-26 Kajima Corp Material for solidifying flimsy ground
JPS57202374A (en) * 1981-06-09 1982-12-11 Masao Tamura Soil hardening agent

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