JPH0753280B2 - Treatment method of excavated shear mixed with air bubbles - Google Patents
Treatment method of excavated shear mixed with air bubblesInfo
- Publication number
- JPH0753280B2 JPH0753280B2 JP1236906A JP23690689A JPH0753280B2 JP H0753280 B2 JPH0753280 B2 JP H0753280B2 JP 1236906 A JP1236906 A JP 1236906A JP 23690689 A JP23690689 A JP 23690689A JP H0753280 B2 JPH0753280 B2 JP H0753280B2
- Authority
- JP
- Japan
- Prior art keywords
- added
- air bubbles
- polymer flocculant
- kneaded
- viscosity
- 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.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/24—Macromolecular compounds
- C04B24/26—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C04B24/2652—Nitrogen containing polymers, e.g. polyacrylamides, polyacrylonitriles
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Excavating Of Shafts Or Tunnels (AREA)
- Treatment Of Sludge (AREA)
Description
【発明の詳細な説明】 (産業上の利用分野) 本発明は土木工事において気泡を注入しながら掘削する
気泡シールド工法や気泡試錐工法より発生する気泡混入
掘削ずりの処理法に関する。Description: TECHNICAL FIELD The present invention relates to a bubble shield method of excavating while injecting bubbles in a civil engineering work and a method of treating a bubble mixed excavation shear generated by a bubble drilling method.
(従来の技術と問題点) 従来、シールド工法等においてはベントナイト泥を使用
し、残土処分が困難であった。これを解決する為、ベン
トナイトに替えて気泡を混入する事により掘削土の流動
性と止水性を確保する気泡シールド工法が提案されてい
る。該気泡混入工法の一般的操作条件は、発泡剤水溶液
あたり3〜30倍の発泡倍率の泡を掘削土の体積あたり10
〜100%容量添加混練するものであり、この様にして得
られた気泡混入掘削ずりのスランプ値は3〜10cm程度を
示す事が多い。気泡シールド工法以外にボーリング等に
おいてもビット部の冷却と掘削ずりの搬出を目的として
孔内に泡を注入する工法も知られている。(Conventional technology and problems) Conventionally, bentonite mud has been used in the shield construction method and the like, and disposal of residual soil has been difficult. In order to solve this problem, a bubble shield construction method has been proposed in which the fluidity and water stoppage of excavated soil are secured by mixing air bubbles in place of bentonite. The general operating condition of the bubble-mixing method is that the foaming agent has a foaming ratio of 3 to 30 times per 10 parts by volume of the excavated soil.
The slump value of the bubble-mixed excavated slip thus obtained is often about 3 to 10 cm. In addition to the bubble shield method, a method of injecting bubbles into the hole is also known in boring and the like for the purpose of cooling the bit part and carrying out excavation shear.
これら気泡混入工法から発生する掘削ずりの処理方法と
して特公昭58−47560号公報には自然報知による消泡が
記載され、特公昭59−49999号公報には消泡材の添加に
よる消泡処理が記載されている。しかし、気泡混入掘削
ずり中にはシルト・粘土分やセルロース系増粘剤を含む
場合が多く、該成分の生成する強固な泥膜は気泡の離脱
を妨害するとともに、脱泡残留物においてもなお流動性
を付与する。この為、単なる消泡処理では未だ十分な対
処法とは言えない。一方特願昭63−259367、特願平1−
13205及び特願平1−13206には発泡剤を含まぬシールド
工法掘削残土に対し高分子凝集剤を添加混練する技術が
記載されている。As a method of treating excavation generated from these bubble-mixing methods, Japanese Patent Publication No. 58-47560 describes defoaming by natural notification, and Japanese Patent Publication No. 59-49999 discloses defoaming treatment by adding antifoaming material. Have been described. However, the silt / clay content and the cellulosic thickener are often contained in the drilling mixture containing bubbles, and the strong mud film produced by these components hinders the removal of bubbles, and also in the defoaming residue. Adds liquidity. For this reason, simple defoaming treatment is not yet sufficient. On the other hand, Japanese Patent Application No. Sho 63-259367, Japanese Patent Application No. 1-
13205 and Japanese Patent Application No. 1-13206 describe a technique in which a polymer flocculant is added and kneaded to the excavated soil left by the shield method, which does not contain a foaming agent.
(発明の課題) 本発明は、短時間で気泡混入掘削ずりを固化し、運搬を
容易にし埋土として使用可能な改質土を得る事ができ
る。簡便な処理方法を提供する事を目的とする。(Problem of the Invention) The present invention can obtain a modified soil that solidifies a bubble-containing excavation shear in a short time, facilitates transportation, and can be used as a buried soil. The purpose is to provide a simple processing method.
また、本発明は気泡混入掘削ずりを改質固化するにあた
り、都市部の狭い敷地からなる施工現場においても、保
管、供給、混合等が容易な薬品及び薬注法を提供する事
を目的とする。Another object of the present invention is to provide a chemical and chemical injection method that facilitates storage, supply, mixing, etc. even in a construction site consisting of a narrow site in an urban area when reforming and solidifying a bubble-containing drilling shear. .
(課題を解決する為の手段) 本発明は気泡混入掘削ずりに、カチオン当量値が2meq/g
以上であるカチオン性有機高分子凝集剤を添加混練する
事により構成される。(Means for Solving the Problem) The present invention has a cation equivalent value of 2 meq / g for excavating gas bubbles.
It is constituted by adding and kneading the above cationic organic polymer flocculant.
本発明に用いるカチオン性有機高分子凝集剤は公知のも
のであって、具体的にはエピハロヒドリン、アルキレン
ジハライド、アルキレン多価エポキサイド等を連結剤と
してアミンまたはアンモニアを縮合させた反応物(特公
昭38−26794、特公昭41−17965、特公昭51−22471、特
公昭56−37844等)又はホルムアルデヒドを連結剤とし
てジシアンジアミド、メラミン、グアニジン等の縮合反
応物あるいはポリエチレンイミン、ポリジメチルジアリ
ルアンモニウムクロライド、ジアルキルアミノアルキル
メタアクリレートあるいはジアルキルアミノアルキルア
クリルアミドの塩及び又はその四級化物の(共)重合対
等を例示する事ができる。The cationic organic polymer flocculant used in the present invention is known, and specifically, a reaction product obtained by condensing an amine or ammonia with epihalohydrin, alkylene dihalide, alkylene polyvalent epoxide, etc. as a linking agent (Japanese Patent Publication No. 38-26794, JP-B-41-17965, JP-B-51-22471, JP-B-56-37844, etc.) or condensation reaction products of dicyandiamide, melamine, guanidine or the like with formaldehyde as a linking agent or polyethyleneimine, polydimethyldiallylammonium chloride, dialkyl. Examples thereof include (co) polymerized pairs of salts of aminoalkyl methacrylates or dialkylaminoalkylacrylamides and / or quaternary products thereof.
本発明に用いるカチオン性有機高分子凝集剤は、電荷の
中和を主たる作用機作とする為、そのカチオン当量値の
高い事が望まれ、少なくとも2meq/g以上のカチオ当量値
を有するものが良好な効果を発揮する。カチオン当量値
の測定方法は通常PH4.0におけるコロイド滴定により求
められる。本発明の実施においては、カチオン性有機高
分子凝集剤の架橋吸着作用も効果に寄与するため、カチ
オン当量値が同等であれば、高分子量の凝集剤の法が少
ない添加量で効果を発揮する。気泡混入掘削ずりとカチ
オン製有機高分子凝集剤の混練法は特に限定されるもの
ではなく、連続ミキサー、強制撹拌ミキサー等の混練機
を使用する他、パワーショベル、バックホウ、スクリュ
ーコンベア等の土木機械を用いて混練する事もできる。
特にシールド機のスクリューコンベア部に注入する工法
は、既設の装置を利用する為、新規の処理用敷地等を必
要とせず都市部における実施は容易となる。The cationic organic polymer flocculant used in the present invention, whose main mechanism of action is to neutralize charge, is desired to have a high cation equivalent value, and one having a cation equivalent value of at least 2 meq / g or more. Exhibits good effects. The cation equivalent value is usually measured by colloid titration in PH4.0. In the practice of the present invention, since the cross-linking and adsorbing action of the cationic organic polymer flocculant also contributes to the effect, if the cation equivalent value is the same, the method of the high molecular weight flocculant exerts the effect with a small addition amount. . The method of kneading the bubble-containing drilling shear and the cation-made organic polymer coagulant is not particularly limited, and a kneader such as a continuous mixer or a forced stirring mixer is used, as well as a civil engineering machine such as a power shovel, a backhoe, or a screw conveyor. It can also be kneaded using.
In particular, the method of injecting into the screw conveyor section of the shield machine uses existing equipment, so it does not require a new processing site, etc., and can be easily implemented in urban areas.
気泡混入掘削ずりと混練するカチオン性有機高分子凝集
剤の添加量は気泡混入掘削ずり1m3に対し、ポリマー純
分0.01〜1kgを使用する。該高分子凝集剤を粉末状態で
添加した場合はママ粉を生じ易く、高性能の撹拌混練装
置を必要とする。気泡混入掘削ずりと簡易に混練する為
には該高分子凝集剤を粘度10,000cp以下の定粘度液の状
態で添加する事が望ましい。液状化する方法としては水
に溶解し、濃度0.5〜50%程度の凝集剤水溶液として添
加する方法が最も安価である。しかし、高含水比のずり
を処理する場合等水分増加を忌避する場合はポリマー微
粒子を油または塩水溶液注に分散させて液状化した高分
子凝集剤が望ましい。また、本発明におけるカチオン性
有機高分子凝集剤の使用法は単独添加に限定されるもの
ではなく、硫酸アルミニウム、ポリ塩化アルミニウム等
の無機凝集剤との併用添加あるいはカチオン性有機高分
子凝集剤添加混練後に高級水性樹脂、アニオン系有機高
分子凝集剤あるいは石灰やセメント等の無機系固化剤を
添加混練する事もできる。The addition amount of the cationic organic polymer flocculant to be kneaded with the aerated excavated shear is 0.01-1 kg of the polymer content for 1 m 3 of the aerated excavated shear. When the polymer flocculant is added in a powder state, mama powder is easily generated and a high performance stirring and kneading device is required. In order to easily knead with the bubble-containing drilling shear, it is desirable to add the polymer coagulant in the state of a constant viscosity liquid having a viscosity of 10,000 cp or less. The most inexpensive method for liquefying is to dissolve it in water and add it as an aqueous coagulant solution having a concentration of about 0.5 to 50%. However, in the case of avoiding an increase in water content such as when processing a high water content shear, a polymer flocculant which is liquefied by dispersing polymer fine particles in an oil or salt solution injection is preferable. Further, the method of using the cationic organic polymer flocculant in the present invention is not limited to single addition, and is added in combination with an inorganic flocculant such as aluminum sulfate and polyaluminum chloride, or a cationic organic polymer flocculant is added. After kneading, a high-grade aqueous resin, an anionic organic polymer flocculant, or an inorganic solidifying agent such as lime or cement may be added and kneaded.
(作用) 本発明は、カチオン性有機高分子凝集剤を気泡混入掘削
ずりに添加混練する事により、粘度粒子等の負電荷を中
和し、凝集させ流動性を除去する事を基本とする。(Function) The present invention is basically based on the fact that a cationic organic polymer coagulant is added and kneaded to a drill mixed with air bubbles to neutralize negative charges such as viscous particles and aggregate to remove fluidity.
気泡周囲の泥膜が(電荷の中和により親水性を失い、凝
集する事によって)破れると、気泡は混練によって容易
に集合し、ずりから放出される。気泡を失い、凝集した
改質土は流動性が無く、運搬や埋土が容易となる。If the mud film around the bubbles breaks (due to loss of hydrophilicity due to charge neutralization and aggregation), the bubbles easily aggregate by kneading and are released from the shear. The modified soil that has lost air bubbles and agglomerated has no fluidity and is easy to transport and fill.
この様な作用は泥中にCMC等のアニオン性増粘剤が存在
する場合でも有効であり、カチオン性有機高分子凝集剤
はこれらアニオン性高分子とイオコンプレックスをつく
り、水不溶性とする事により、増粘作用を消失させる。Such an action is effective even when an anionic thickening agent such as CMC is present in the mud, and the cationic organic polymer flocculant forms an ion complex with these anionic polymers to make them water-insoluble. , To eliminate the thickening effect.
この様な効果は従来の消泡剤には全く期待する事のでき
ないものであり、本発明の優位性を立証するものであ
る。Such an effect cannot be expected from conventional antifoaming agents, and proves the superiority of the present invention.
(実施例) 以下に実施例を用いて本発明を具体的に説明する。(Example) Hereinafter, the present invention will be specifically described with reference to examples.
合成例−1 撹拌器、温度計、還流冷却器、窒素導入管を備えた1
の五つ口セパラブルフラスコに、アクリロイルオキシル
エチルトリメチルアンモニウムクロライドのホモポリマ
ー6g、無水硫酸ナトリウム42g、無水硫酸アルミニウム9
8g、イオン交換水253g、アクリルアミド33.5g、アクリ
ルアミドプロピルジメチルベンジルアンモニウムクロラ
イド22.5gを仕込み、50℃に加温して窒素置換をした。Synthesis example-1 1 equipped with a stirrer, a thermometer, a reflux condenser, and a nitrogen introducing pipe
In a 5-neck separable flask, 6 g of homopolymer of acryloyloxylethyltrimethylammonium chloride, 42 g of anhydrous sodium sulfate, 9 g of anhydrous aluminum sulfate.
8 g, ion-exchanged water (253 g), acrylamide (33.5 g) and acrylamidopropyldimethylbenzylammonium chloride (22.5 g) were charged, and the mixture was heated to 50 ° C. and purged with nitrogen.
これに。2.2′−アゾビス(2−アミジノプロパン)塩
酸塩の10%水溶液1mlを加え、撹拌下50℃で10時間重合
すると、ポリマー微粒子の分散液が得られた。to this. A dispersion of fine polymer particles was obtained by adding 1 ml of a 10% aqueous solution of 2.2'-azobis (2-amidinopropane) hydrochloride and conducting polymerization at 50 ° C for 10 hours with stirring.
これを試料−1と呼ぶ。この製品の粘度は25℃で2020cp
であり、1規定硫酸ナトリウム水溶液にポリマー濃度0.
5%に溶解した液の粘度は25℃で10cpdであり、PH4.0に
おけるカチオン当量値は2.6mep/gであった。This is referred to as Sample-1. The viscosity of this product is 2020cp at 25 ℃
And the polymer concentration was 0.
The viscosity of the solution dissolved in 5% was 10 cpd at 25 ° C, and the cation equivalent value at PH4.0 was 2.6 mep / g.
合成例−2 合成例−1に使用したと同様のセパラブルフラスコに中
油220gを仕込み、ICI社製ハイパーマーB−246を5g、ソ
ルビタンモノオレート10gを溶解した。別にアクリルア
ミド102gとメタクリロイルオキシエチルトリメチルアン
モニウムクロライド198gをイオン交換水213gに溶解した
モノマー溶液を調整後、前述のセパラブルフラスコ内に
注入し撹拌した。Synthesis Example-2 220 g of medium oil was charged in the same separable flask as used in Synthesis Example-1, 5 g of ICI Hypermer B-246 and 10 g of sorbitan monooleate were dissolved. Separately, a monomer solution prepared by dissolving 102 g of acrylamide and 198 g of methacryloyloxyethyltrimethylammonium chloride in 213 g of ion-exchanged water was prepared, and then poured into the aforementioned separable flask and stirred.
30分間窒素置換をした後、内温を45℃に調整後、アゾビ
スイソブチロニトリル50mgを含むアセトン溶液を添加し
重合を開始した。発熱を認めなくなってから昇温し、5
時間65℃に保持し重合を完結させた。得られたエマルジ
ョンにポリオキシエチレンノニルフエニルエーテル20g
とポリオキシエチレンソルビタントリオレート20gを加
えた液を試料−2と呼ぶ。試料−2の粘度は25℃にて98
0cpであり、1規定食塩水にポリマー濃度0.5%に溶解し
た液の25℃における粘度は25cpであり、PH4.0における
カチオ当量値は3.1meq/gであった。After purging with nitrogen for 30 minutes, the internal temperature was adjusted to 45 ° C., and then an acetone solution containing 50 mg of azobisisobutyronitrile was added to initiate polymerization. After the exotherm is no longer recognized, the temperature is raised to 5
The temperature was kept at 65 ° C. to complete the polymerization. 20 g of polyoxyethylene nonylphenyl ether was added to the obtained emulsion.
And a solution containing 20 g of polyoxyethylene sorbitan trioleate are referred to as Sample-2. The viscosity of Sample-2 is 98 at 25 ℃
The viscosity at 25 ° C. of the liquid having a polymer concentration of 0.5% dissolved in 1N saline was 25 cp, and the Catio equivalent value at PH 4.0 was 3.1 meq / g.
合成例−3 撹拌装置、温度計、還流冷却器及び500mlの滴下漏斗を
備えた1の四つ口セパラブルフラスコにエピクロルヒ
ドリン370gを仕込み、撹拌下、内温を10〜45℃に調整し
ながらジメチルアミン40%水溶液400gを滴下した。2時
間を要して滴下終了後、ペンタエチレンヘキサミン40g
を添加し、内温65〜70℃に保持し縮合反応を行った。内
容物の粘度が15,000cpに増粘した状態で25%硫酸水溶液
を加え、PHを3とし縮合反応を停止させた後、得られた
ポリカチオン水溶液をポリマー濃度50%に希釈した。こ
れを試料−3と呼ぶ。Synthesis Example-3 370 g of epichlorohydrin was charged into a 4-neck separable flask equipped with a stirrer, a thermometer, a reflux condenser and a 500-ml dropping funnel, and dimethyl was added under stirring with adjusting the internal temperature to 10 to 45 ° C. 400 g of 40% aqueous amine solution was added dropwise. After dropping for 2 hours, 40g of pentaethylenehexamine
Was added and the internal temperature was maintained at 65 to 70 ° C to carry out the condensation reaction. With the viscosity of the contents increased to 15,000 cp, a 25% sulfuric acid aqueous solution was added to adjust pH to 3 to stop the condensation reaction, and then the obtained polycation aqueous solution was diluted to a polymer concentration of 50%. This is referred to as Sample-3.
25℃における試料−3の粘度は5300cpであり、ポリマー
のカチオン当量値は7.1meq/gであった。The viscosity of Sample-3 at 25 ° C was 5300 cp, and the cation equivalent value of the polymer was 7.1 meq / g.
合成例−4 市販のメタクリロイルオキシエチルトリメチルアンモニ
ウムクロライドとアクリルアミドの(共)重合物である
粉末高分子凝集剤の2%水溶液を調整し試験に供した。
各試料名と物性値を下表に示す。但し、表中の0.5%粘
度とは1規定食塩水中にポリマー濃度0.5%に溶解した
液の25℃における粘度である。Synthesis Example-4 A 2% aqueous solution of a commercially available powdery polymer flocculant, which is a (co) polymer of methacryloyloxyethyltrimethylammonium chloride and acrylamide, was prepared and tested.
The sample names and physical properties are shown in the table below. However, the 0.5% viscosity in the table is the viscosity at 25 ° C. of a liquid having a polymer concentration of 0.5% dissolved in 1N saline.
実施例−1 含水比41%、シルト粘土分80%の土20kgを強制練りコン
クリートミキサーに入れ、ポリオキシエチレンアルキル
スルフオン酸ナトリウムの0.3%水溶液の7倍発泡物を
7加え2分間混練した。 Example 1 20 kg of soil having a water content ratio of 41% and a silt clay content of 80% was placed in a forced kneading concrete mixer, and 7 times a 7-fold foam of a 0.3% aqueous solution of sodium polyoxyethylene alkylsulfonate was added and kneaded for 2 minutes.
得られた気泡混入土のスランプ値は5.5cmであった。気
泡混入土にカチオン性有機高分子凝集剤を添加し、2分
間混練後、スランプ値を測定した結果を表−2に示す。The slump value of the aerated soil thus obtained was 5.5 cm. A cationic organic polymer flocculant was added to the aerated soil, the mixture was kneaded for 2 minutes, and the slump value was measured. The results are shown in Table-2.
薬品の添加量は有姿表示である。The amount of chemicals added is shown in physical form.
実施例−2 2%水溶液の粘度が5000cpであるカルボキシメチルセル
ローズをポリマー濃度0.5%の水溶液としポリオキシエ
チレンアルキルスルホン酸ナトリウムを水に対し、0.1
重量%添加溶解した液を撹拌機により6.5倍に発砲させ
た。強制練りコンクリートミキサーに含水比12%、FM3.
11の市販砂18kg及び含水比52%、シルト粘土分48%の赤
土2kgを仕込み、上記発砲物6を加えて1分間混練し
た。得られた気泡混入土のスランプ値は6cmであった。
気泡混入土にカチオン性高分子凝集剤を添加し、2分間
混練後、スランプ値を測定した結果を表−3に示す。 Example-2 Carboxymethyl cellulose having a viscosity of 5000 cp of a 2% aqueous solution was used as an aqueous solution having a polymer concentration of 0.5%, and sodium polyoxyethylene alkylsulfonate was added to water in an amount of 0.1.
A solution in which the weight% was added and dissolved was fired 6.5 times with a stirrer. Moisture content 12%, FM3.
11 kg of commercially available sand of 11 and 2 kg of red soil having a water content ratio of 52% and a silt clay content of 48% were charged, the above-mentioned foam 6 was added, and the mixture was kneaded for 1 minute. The slump value of the aerated soil thus obtained was 6 cm.
The cationic polymer flocculant was added to the aerated soil, the mixture was kneaded for 2 minutes, and the slump value was measured. The results are shown in Table 3.
薬品の添加量は有姿表示である。The amount of chemicals added is shown in physical form.
Claims (2)
カチオン性高分子凝集剤を、気泡混入掘削ずり1m3に対
し0.01〜1kg添加混練する事により、脱水工程を経る事
無く流動性を消失させる事を特徴とする気泡混入掘削ず
りの処理法。1. A water-soluble cationic polymer flocculant having a cation equivalent value of 2 meq / g or more is added and kneaded in an amount of 0.01 to 1 kg per 1 m 3 of aeration mixed with air bubbles, so that fluidity can be obtained without a dehydration step. A method for treating excavated rocks containing air bubbles, which is characterized by eliminating water.
cp以下の液状で添加混練する事を特徴とする請求項1に
記載の気泡混入掘削ずりの処理法。2. A cationic organic polymer flocculant having a viscosity of 10,000
The method for treating excavated mixture containing bubbles according to claim 1, characterized in that the mixture is added and kneaded in a liquid form of cp or less.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1236906A JPH0753280B2 (en) | 1989-09-14 | 1989-09-14 | Treatment method of excavated shear mixed with air bubbles |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1236906A JPH0753280B2 (en) | 1989-09-14 | 1989-09-14 | Treatment method of excavated shear mixed with air bubbles |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03100295A JPH03100295A (en) | 1991-04-25 |
| JPH0753280B2 true JPH0753280B2 (en) | 1995-06-07 |
Family
ID=17007507
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1236906A Expired - Lifetime JPH0753280B2 (en) | 1989-09-14 | 1989-09-14 | Treatment method of excavated shear mixed with air bubbles |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0753280B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006265885A (en) * | 2005-03-23 | 2006-10-05 | Kurita Water Ind Ltd | Treatment method of construction waste mud generated by bubble shield method |
| JP2020037821A (en) * | 2018-09-05 | 2020-03-12 | テクニカ合同株式会社 | Modification method of foam mixed soil |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH11323335A (en) * | 1998-05-14 | 1999-11-26 | Nippon Shokubai Co Ltd | How to improve hydrated soil |
| JP4620824B2 (en) * | 2000-02-08 | 2011-01-26 | 株式会社大林組 | Manufacturing method of backfill soil |
| FR2937032B1 (en) * | 2008-10-10 | 2011-06-03 | Lafarge Sa | COMPOSITION BASED ON HYDRAULIC AND / OR POUZZOLANIC MATERIAL OTHER THAN CLINKER |
| JP5666825B2 (en) * | 2010-04-30 | 2015-02-12 | 前田建設工業株式会社 | Bent boring method and drilling device used therefor |
| JP5534597B2 (en) * | 2010-07-21 | 2014-07-02 | 株式会社大林組 | Excavation soil treatment method in bubble shield construction |
| JP6619193B2 (en) * | 2015-09-30 | 2019-12-11 | 太平洋セメント株式会社 | Residual soil processing material and processing method of residual soil |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5746400A (en) * | 1980-09-05 | 1982-03-16 | Toshiba Corp | Memory device |
-
1989
- 1989-09-14 JP JP1236906A patent/JPH0753280B2/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006265885A (en) * | 2005-03-23 | 2006-10-05 | Kurita Water Ind Ltd | Treatment method of construction waste mud generated by bubble shield method |
| JP2020037821A (en) * | 2018-09-05 | 2020-03-12 | テクニカ合同株式会社 | Modification method of foam mixed soil |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH03100295A (en) | 1991-04-25 |
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