JPH1161126A - Grouting material - Google Patents
Grouting materialInfo
- Publication number
- JPH1161126A JPH1161126A JP22658497A JP22658497A JPH1161126A JP H1161126 A JPH1161126 A JP H1161126A JP 22658497 A JP22658497 A JP 22658497A JP 22658497 A JP22658497 A JP 22658497A JP H1161126 A JPH1161126 A JP H1161126A
- Authority
- JP
- Japan
- Prior art keywords
- liquid
- fine powder
- injection material
- ground injection
- solution
- 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
Links
- 239000000463 material Substances 0.000 title claims abstract description 64
- 239000000843 powder Substances 0.000 claims abstract description 47
- 238000006703 hydration reaction Methods 0.000 claims abstract description 19
- 230000036571 hydration Effects 0.000 claims abstract description 17
- 239000007788 liquid Substances 0.000 claims abstract description 16
- 239000003112 inhibitor Substances 0.000 claims abstract description 15
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims abstract description 14
- 235000019353 potassium silicate Nutrition 0.000 claims abstract description 7
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000002253 acid Substances 0.000 claims abstract description 4
- 150000005846 sugar alcohols Chemical class 0.000 claims abstract description 4
- 150000007513 acids Chemical class 0.000 claims abstract description 3
- 150000001642 boronic acid derivatives Chemical class 0.000 claims abstract description 3
- 150000001991 dicarboxylic acids Chemical class 0.000 claims abstract description 3
- 238000002347 injection Methods 0.000 claims description 32
- 239000007924 injection Substances 0.000 claims description 32
- 229910019142 PO4 Inorganic materials 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- -1 oxycarboxylates Chemical class 0.000 claims description 4
- 235000021317 phosphate Nutrition 0.000 claims description 4
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 3
- 235000000346 sugar Nutrition 0.000 claims description 3
- 239000000725 suspension Substances 0.000 claims description 3
- 150000008163 sugars Chemical class 0.000 claims description 2
- 150000002222 fluorine compounds Chemical class 0.000 claims 1
- 239000004568 cement Substances 0.000 abstract description 21
- 239000002245 particle Substances 0.000 abstract description 16
- 239000002893 slag Substances 0.000 abstract description 14
- 239000010440 gypsum Substances 0.000 abstract description 13
- 229910052602 gypsum Inorganic materials 0.000 abstract description 13
- 238000002156 mixing Methods 0.000 abstract description 13
- 239000002002 slurry Substances 0.000 abstract description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 8
- 238000004898 kneading Methods 0.000 abstract description 4
- 239000000377 silicon dioxide Substances 0.000 abstract description 3
- 239000000084 colloidal system Substances 0.000 abstract description 2
- 239000011882 ultra-fine particle Substances 0.000 abstract description 2
- 230000032683 aging Effects 0.000 abstract 1
- 150000001720 carbohydrates Chemical class 0.000 abstract 1
- 229910052681 coesite Inorganic materials 0.000 abstract 1
- 229910052906 cristobalite Inorganic materials 0.000 abstract 1
- 150000004673 fluoride salts Chemical class 0.000 abstract 1
- 125000002467 phosphate group Chemical class [H]OP(=O)(O[H])O[*] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 235000012239 silicon dioxide Nutrition 0.000 abstract 1
- 229910052682 stishovite Inorganic materials 0.000 abstract 1
- 229910052905 tridymite Inorganic materials 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 230000001143 conditioned effect Effects 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000001879 gelation Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- AEQDJSLRWYMAQI-UHFFFAOYSA-N 2,3,9,10-tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline Chemical compound C1CN2CC(C(=C(OC)C=C3)OC)=C3CC2C2=C1C=C(OC)C(OC)=C2 AEQDJSLRWYMAQI-UHFFFAOYSA-N 0.000 description 1
- QJZYHAIUNVAGQP-UHFFFAOYSA-N 3-nitrobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid Chemical compound C1C2C=CC1C(C(=O)O)C2(C(O)=O)[N+]([O-])=O QJZYHAIUNVAGQP-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229940043430 calcium compound Drugs 0.000 description 1
- 150000001674 calcium compounds Chemical class 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 150000004683 dihydrates Chemical class 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 239000004021 humic acid Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 150000002913 oxalic acids Chemical class 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000012254 powdered material Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 125000005372 silanol group Chemical group 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- HELHAJAZNSDZJO-OLXYHTOASA-L sodium L-tartrate Chemical compound [Na+].[Na+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O HELHAJAZNSDZJO-OLXYHTOASA-L 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 235000011083 sodium citrates Nutrition 0.000 description 1
- 239000000176 sodium gluconate Substances 0.000 description 1
- 235000012207 sodium gluconate Nutrition 0.000 description 1
- 229940005574 sodium gluconate Drugs 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 239000001433 sodium tartrate Substances 0.000 description 1
- 229960002167 sodium tartrate Drugs 0.000 description 1
- 235000011004 sodium tartrates Nutrition 0.000 description 1
- 239000011973 solid acid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
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
- C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
- C04B28/24—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing alkyl, ammonium or metal silicates; containing silica sols
-
- 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
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/00474—Uses not provided for elsewhere in C04B2111/00
- C04B2111/00732—Uses not provided for elsewhere in C04B2111/00 for soil stabilisation
-
- 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
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/70—Grouts, e.g. injection mixtures for cables for prestressed concrete
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Soil Conditioners And Soil-Stabilizing Materials (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、懸濁型の地盤注入
材に関するものであり、さらに詳しくは懸濁型でかつ緩
結型の地盤注入材において、水硬性を有する粉体材料の
スラリーの練り置き時間が、ゲルタイム等の性能に影響
を及ぼしにくい地盤注入材に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a suspension type ground injection material, and more particularly, to a suspension type ground injection material, which comprises a slurry of hydraulic material powdery material. The present invention relates to a ground injection material whose kneading time hardly affects performance such as gel time.
【0002】[0002]
【従来の技術】地盤注入材は、ダムの基礎、大型地下構
造物等の岩盤の強化・止水ならびに砂地盤の液状化対策
等を目的とした恒久的な地盤改良方法として注目を浴び
ている。懸濁型の地盤注入材は、懸濁性の反応材、例え
ばセメント粉末を使用するものであり、そのためにゲル
タイムが非常に短い瞬結型のものが多いのが現状であ
る。このような地盤注入材は、一般的に水硬性を有する
粉末材料を主成分とするスラリーからなるA液を調製
し、これとは別にシリカゾルや水ガラスを主成分とする
B液を調製し、使用直前に両者を混合して調製されてい
る。また、A液およびB液を別々に調製せずにその場で
両液の混合物を調製する方法も知られている。2. Description of the Related Art Ground injection materials are attracting attention as a permanent soil improvement method for the purpose of strengthening and stopping water in rocks such as dam foundations and large underground structures, and countermeasures against liquefaction of sand grounds. . The suspension-type ground injection material uses a suspension-type reaction material, for example, cement powder. Therefore, at present, there are many instantaneous setting types having a very short gel time. Such a ground injection material generally prepares a liquid A composed of a slurry mainly composed of a powder material having hydraulic properties, and separately prepares a liquid B composed mainly of silica sol or water glass, It is prepared by mixing both immediately before use. There is also known a method of preparing a mixture of the solutions A and B on the spot without separately preparing the solutions A and B.
【0003】ゲルタイムが長い緩結型の地盤注入材を調
製する場合、A液およびB液を混合するまでの、A液が
スラリーとして置かれる時間(練り置き時間)がその緩
結性に大きな影響を及ぼすことが知られている。すなわ
ち、練り置き時間が増加すると、A液のスラリー中の水
和反応が進行したり、スラリーのpHが高まることなど
により、B液と混合した際の地盤注入材のゲル化が促進
される。このゲル化の促進は、地盤注入材のゲルタイム
を縮めるだけではなく、地盤注入材の浸透性を低下させ
たりするなど、望まれない結果を招くことになる。[0003] In the case of preparing a loose-type ground injection material having a long gel time, the time during which the solution A is placed as a slurry (kneading time) until the solution A and the solution B are mixed has a great influence on the loosening property. It is known to exert That is, if the mixing time is increased, the hydration reaction of the solution A in the slurry proceeds, and the pH of the slurry is increased, thereby promoting the gelation of the ground injection material when mixed with the solution B. This promotion of gelation not only shortens the gel time of the ground injection material, but also results in undesirable results such as lowering the permeability of the ground injection material.
【0004】[0004]
【発明が解決しようとする課題】したがって本発明の目
的は、懸濁型でかつ緩結型の地盤注入材において、水硬
性を有する粉体材料のスラリーの練り置き時間が、ゲル
タイム等の性能に影響を及ぼしにくい地盤注入材を提供
することにある。SUMMARY OF THE INVENTION Accordingly, an object of the present invention is to provide a suspension-type and slow-setting type soil injection material in which the kneading time of the slurry of the powdery material having hydraulic properties is reduced by the performance such as gel time. An object of the present invention is to provide a ground injection material that is hardly affected.
【0005】[0005]
【課題を解決するための手段】本発明者らは鋭意検討の
結果、上記のような従来の課題を解決することができ
た。すなわち本発明は、水硬性を有する粉末材料を主成
分とするスラリーからなるA液と、シリカゾルおよび/
または水ガラスを主成分とするB液とからなる懸濁型の
地盤注入材であって、前記A液に前記粉末材料の水和を
抑制する水和抑制剤を配合したことを特徴とする地盤注
入材を提供するものである。Means for Solving the Problems As a result of intensive studies, the present inventors were able to solve the above-mentioned conventional problems. That is, the present invention provides a solution A comprising a slurry mainly containing a powder material having hydraulic properties, a silica sol and / or
Or a suspension-type ground injection material composed of liquid B containing water glass as a main component, wherein the liquid A is mixed with a hydration inhibitor that suppresses hydration of the powder material. It is intended to provide an injection material.
【0006】また本発明は、水和抑制剤が、フッ化物、
リン酸塩、ホウ酸塩、オキシカルボン酸塩、ジカルボン
酸類、ケトカルボン酸類、糖アルコール類および糖類か
らなる群から選択された少なくとも1種である前記の地
盤注入材を提供するものである。[0006] Further, the present invention provides a method for producing a hydration inhibitor, comprising:
An object of the present invention is to provide the above ground injection material, which is at least one selected from the group consisting of phosphates, borates, oxycarboxylates, dicarboxylic acids, ketocarboxylic acids, sugar alcohols and sugars.
【0007】さらに本発明は、水和抑制剤が、粉末材料
に対して0.05〜10重量%の割合で配合される前記
の地盤注入材を提供するものである。Further, the present invention provides the above-mentioned ground injection material, wherein the hydration inhibitor is blended at a ratio of 0.05 to 10% by weight with respect to the powder material.
【0008】[0008]
(B液)本発明で使用するB液は、シリカゾルおよび/
または水ガラスを主成分とするものである。シリカゾル
は、粒子の大きさが例えば1〜100mμ(0.1
μ)、好ましくは5〜50mμであって、沈降せずに溶
媒に安定的に分散した超微粒子のコロイドであり、その
溶質の主成分がシリカである。シリカゾルは、シリカ粒
子の安定性および地盤注入材としての各種性能(浸透性
等)の点から、シリカゾルの主な特性として、ナトリウ
ム、アンモニウム、塩素等の安定化イオンを持ち、また
は表面にアルミニウムイオンのような電価の異なる異種
金属を配位して固体酸を形成させて、表面のシラノール
基の解離を広いpH範囲で持たせることにより安定性を
付与したものがよい。水ガラスは市販されているものを
そのまま使用することができる。シリカゾルを使用する
場合は、市販されているものをそのまま使用することが
できるが、SiO2濃度10〜60重量%、平均粒子径
3〜50mμ、粘度は50cps(25℃)以下のもの
がよい。(Solution B) The Solution B used in the present invention comprises silica sol and / or
Alternatively, the main component is water glass. The silica sol has a particle size of, for example, 1 to 100 μm (0.1
μ), preferably 5 to 50 μm, and is a colloid of ultrafine particles stably dispersed in a solvent without sedimentation, and the main component of the solute is silica. Silica sol has stabilizing ions such as sodium, ammonium, and chlorine as main characteristics of the silica sol, or aluminum ion on the surface, in view of the stability of silica particles and various performances (penetration, etc.) as a ground injection material. It is preferable that a solid acid is formed by coordinating different metals having different electric valencies such as described above and the dissociation of silanol groups on the surface is imparted in a wide pH range to impart stability. Commercially available water glass can be used as it is. When silica sol is used, commercially available silica sol can be used as it is, but it is preferable that the SiO 2 concentration is 10 to 60% by weight, the average particle diameter is 3 to 50 mμ, and the viscosity is 50 cps (25 ° C.) or less.
【0009】(A液)本発明で使用するA液は、水硬性
を有する粉末材料を主成分とするスラリーからなる。粉
末材料は、とくに制限されないが、セメントクリンカー
および/またはセメント微粉末、高炉スラグ微粉末およ
び石膏微粉末を含む粉末材料を使用すれば、浸透性が向
上し好ましい。これらの各種成分のさらに好適な態様に
ついて、以下、さらに説明する。(Solution A) The Solution A used in the present invention comprises a slurry mainly composed of a powder material having hydraulic properties. The powder material is not particularly limited. However, it is preferable to use a powder material containing cement clinker and / or cement fine powder, blast furnace slag fine powder, and gypsum fine powder because permeability is improved. More preferred embodiments of these various components will be further described below.
【0010】セメントクリンカーおよび/またはセメン
ト微粉末(以下、セメント微粉末という)としては、例
えば普通、早強、超早強、中庸熱、耐硫酸塩等があげら
れ、中でも好ましくは浸透性と強度発現の両者を満足す
るものとして普通あるいは早強が好ましい。なお、この
セメント微粉末は、混合セメント由来のものは、各成分
の粒度を制御できないという理由から除くものとする。The cement clinker and / or cement fine powder (hereinafter referred to as cement fine powder) includes, for example, ordinary, fast-strength, ultra-fast-strength, moderate heat, and sulfate resistance. Normal or early strength is preferred as satisfying both of the expressions. In addition, this cement fine powder shall not be derived from the mixed cement because it cannot control the particle size of each component.
【0011】セメント微粉末の粒径は、最大粒径が1
0.5μm以下であり、且つ2.2μm通過分がセメン
ト微粉末全体に対して50容量%以下、好ましくは40
容量%以下がよい。The maximum particle size of the cement fine powder is 1
0.5 μm or less, and the passage of 2.2 μm is 50% by volume or less, preferably 40% by volume, based on the whole cement fine powder.
The capacity% or less is good.
【0012】高炉スラグは、急冷した高炉水さいスラグ
が好適である。高炉スラグ微粉末の粒径は、最大粒径が
10.5μm以下がよく、且つ2.2μm通過分が高炉
スラグ微粉末全体に対して50容量%以下、好ましくは
40容量%以下がよい。The blast furnace slag is preferably a rapidly cooled blast furnace water slag. The particle size of the blast-furnace slag fine powder is preferably such that the maximum particle size is 10.5 μm or less, and the passage of 2.2 μm is 50% by volume or less, preferably 40% by volume or less based on the whole blast-furnace slag fine powder.
【0013】石膏微粉末は、二水石膏、無水石膏が好適
である。石膏微粉末の粒径は、最大粒径10.5μm以
下がよい。The gypsum fine powder is preferably gypsum dihydrate or anhydrous gypsum. The maximum particle size of the gypsum fine powder is preferably 10.5 μm or less.
【0014】なお、原料のセメントクリンカーおよび/
またはセメントと石膏とを混合して粉砕する場合は、混
合物が最大粒径10.5μm以下、且つ2.2μm通過
分50容量%以下を満足するのが望ましい。The raw material cement clinker and / or
Alternatively, in the case where cement and gypsum are mixed and pulverized, the mixture desirably satisfies a maximum particle size of 10.5 μm or less and a volume of 2.2 μm passage of 50% by volume or less.
【0015】(配合割合)上記のような粉末材料を使用
する場合、その配合割合は、セメント微粉末0〜50重
量部(石膏を除く)、高炉スラグ微粉末50〜100重
量部および石膏微粉末をSO3換算で0.5〜3.0重
量部含有するのがよい。なお、石膏微粉末は、セメント
中の石膏を考慮に入れるものとする。(Blending ratio) When the above powder materials are used, the blending ratio is such that 0 to 50 parts by weight of cement fine powder (excluding gypsum), 50 to 100 parts by weight of blast furnace slag fine powder and gypsum fine powder In an amount of 0.5 to 3.0 parts by weight in terms of SO 3 . Note that the gypsum fine powder takes into account gypsum in cement.
【0016】また粉末材料には、必要に応じてフライア
ッシュ等のポゾラン物質や、炭酸カルシウム、消石灰等
のカルシウム化合物を、好ましくは最大粒径が10.5
μm以下、2.2μm通過分がその全体成分に対して5
0容量%以下の粒度として、高炉スラグ微粉末に内割り
で最大10重量部程度置換して用いることができる。The powdered material may optionally contain a pozzolanic substance such as fly ash or a calcium compound such as calcium carbonate or slaked lime, preferably having a maximum particle size of 10.5.
μm or less and 2.2 μm pass through is 5% of the total components.
As a particle size of 0% by volume or less, it can be used by substituting about 10 parts by weight at the maximum for blast furnace slag fine powder.
【0017】さらに粉末材料において、1μm以下の粒
子の量は15容量%以下であることが、浸透性の点から
望ましい。Further, in the powder material, the amount of particles having a particle size of 1 μm or less is preferably 15% by volume or less from the viewpoint of permeability.
【0018】(粉末材料の製造)上記の各種成分を使用
して粉末材料を製造する場合、少なくとも高炉スラグと
その他各成分とを個別に粉砕・分級する必要がある。こ
のようにすれば、被粉砕性の相違による超微粉へのセメ
ント微粉末等の偏り並びに過粉砕によるセメント微粉末
のアモルファス化を防ぐこともできる。(Production of powder material) In the case of producing a powder material using the above-mentioned various components, it is necessary to separately pulverize and classify at least the blast furnace slag and other components. In this way, it is possible to prevent the cement fine powder from being biased to the ultra fine powder due to the difference in grindability, and to prevent the cement fine powder from being amorphous due to over-pulverization.
【0019】具体的に述べると、例えば、少なくとも高
炉スラグを他の成分とは別個に粉砕且つ分級し、この後
に得られた高炉スラグ微粉末を分級済みの他の成分と混
合することができる。More specifically, for example, at least blast furnace slag can be pulverized and classified separately from other components, and then the resulting blast furnace slag fine powder can be mixed with the classified other components.
【0020】また、セメント成分と石膏とを混合粉砕且
つ分級し、これとは別に高炉スラグを粉砕且つ分級し、
この後に得られた各成分を混合してもよい。Further, the cement component and the gypsum are mixed and crushed and classified, and separately from this, blast furnace slag is crushed and classified,
The components obtained after this may be mixed.
【0021】さらに、セメント成分、高炉スラグおよび
石膏を、それぞれ個別に粉砕且つ分級し、この後に各成
分を集合し混合してもよい。Further, the cement component, the blast furnace slag and the gypsum may be individually ground and classified, and thereafter, the components may be assembled and mixed.
【0022】(水和抑制剤)本発明に使用される水和抑
制剤は、A液における水和反応によるCaイオンの溶出
を抑制できるものから種々選択することができる。その
例としては、無機系としてフッ化物、リン酸塩、ホウ酸
塩、有機系としてオキシカルボン酸塩、ジカルボン酸
類、ケトカルボン酸類、糖アルコール類および糖類の少
なくとも1種以上を含むことが好ましい。さらに具体的
には、リン酸二ナトリウム、クエン酸、クエン酸ナトリ
ウム、グルコン酸、グルコン酸ナトリウム、酒石酸、酒
石酸ナトリウム、ショ糖、フミン酸等が挙げられる。(Hydration Inhibitor) The hydration inhibitor used in the present invention can be variously selected from those capable of suppressing the elution of Ca ions due to the hydration reaction in the solution A. For example, it is preferable to contain at least one or more of fluoride, phosphate, borate as an inorganic material, and oxycarboxylate, dicarboxylic acid, ketocarboxylic acid, sugar alcohol and sugar as an organic material. More specifically, examples include disodium phosphate, citric acid, sodium citrate, gluconic acid, sodium gluconate, tartaric acid, sodium tartrate, sucrose, humic acid, and the like.
【0023】水和抑制剤は、A液に添加することが有効
であり、さらに好ましくはA液の調整水に予め溶解して
おくことが好適である。It is effective to add the hydration inhibitor to the solution A, and it is more preferable to dissolve the hydration inhibitor in the conditioned water of the solution A in advance.
【0024】水和抑制剤の配合割合は、地盤注入材とし
ての性能(特に固結強度の発現性)を損なわない程度で
あれば特に限定されるものではないが、好ましくは粉末
材料に対して、0.05〜10重量%が好適である。The mixing ratio of the hydration inhibitor is not particularly limited as long as it does not impair the performance as a ground injection material (especially, the development of compaction strength). , 0.05 to 10% by weight is preferred.
【0025】本発明の地盤注入材において、ゲルタイム
を調整することを目的として、A液およびB液の少なく
とも一方にゲルタイム調整剤を配合することもできる。
このゲルタイム調整剤としては、アルカリ金属やアルカ
リ土類金属の重炭酸塩、炭酸塩、リン酸塩やシュウ酸、
アンモニウム塩等の少なくとも1種以上が挙げられ、さ
らに具体的には炭酸水素ナトリウム(NaHCO3)、
炭酸ナトリウム(Na2CO3)等が挙げられる。また炭
酸ガスを吹き込むことも有効である。さらに好ましく
は、水に対する溶解度の高いものが好適である。In the ground injection material of the present invention, for the purpose of adjusting the gel time, a gel time adjusting agent may be blended with at least one of the solution A and the solution B.
Examples of the gel time adjusting agent include bicarbonates, carbonates, phosphates and oxalic acids of alkali metals and alkaline earth metals,
At least one or more of ammonium salts and the like, and more specifically, sodium hydrogen carbonate (NaHCO 3 ),
And sodium carbonate (Na 2 CO 3 ). It is also effective to blow carbon dioxide gas. More preferably, those having high solubility in water are suitable.
【0026】ゲルタイム調整剤は、B液に添加してもよ
いが、A液に添加することが有効であり、さらに好まし
くはA液の調整水に予め溶解しておくことが好適であ
る。ゲルタイム調整剤をA液の調整水に予め溶解してお
く場合、A液における粉末材料濃度を高めたほうが、よ
り効果的であり好適である。The gel time adjusting agent may be added to the solution B, but it is effective to add it to the solution A, and it is more preferable to dissolve it in the conditioned water of the solution A in advance. When the gel time adjuster is dissolved in the conditioned water of the solution A in advance, it is more effective and preferable to increase the powder material concentration in the solution A.
【0027】ゲルタイム調整剤の添加量は、地盤注入材
としての性能を損なわない程度であれば特に限定される
ものではないが、好ましくはシリカゾルおよび粉末材料
の固形分の合計に対し、1〜30重量%が好適である。The amount of the gel time adjusting agent is not particularly limited as long as the performance as a ground injection material is not impaired, but is preferably from 1 to 30 with respect to the total solid content of the silica sol and the powder material. % By weight is preferred.
【0028】水和抑制剤およびゲルタイム調整剤は、市
販の試薬などを用いることもできるが、材料費の低減と
いう観点から、工業用の製品もしくは天然に算出する製
品を用いてもよい。As the hydration inhibitor and the gel time adjuster, commercially available reagents and the like can be used, but from the viewpoint of reducing material costs, industrial products or products calculated naturally can be used.
【0029】(本発明の地盤注入材の調製)本発明の地
盤注入材は、A液およびB液を混合することにより調製
できる。これらの配合割合は、特に限定されるものでは
ないが、粉末材料:シリカゾルおよび/または水ガラス
が、重量換算で1:9〜9:1、好ましくは5:5〜
8:2になるように両者を配合することが好適である。
また、水分/固形分の重量比は、各液の調整水を加えた
地盤注入材全体として200%〜1500%が好まし
い。(Preparation of Ground Injection Material of the Present Invention) The ground injection material of the present invention can be prepared by mixing solution A and solution B. The mixing ratio of these is not particularly limited, but the powder material: silica sol and / or water glass is 1: 9 to 9: 1 by weight conversion, preferably 5: 5 to 5: 1.
It is preferable to mix both such that the ratio becomes 8: 2.
Further, the weight ratio of water / solid content is preferably 200% to 1500% for the whole ground injection material to which the adjusted water of each liquid is added.
【0030】[0030]
【実施例】以下、本発明を実施例によって説明するが、
これらの実施例は本発明の一例に過ぎず、これらによっ
て限定されるものではない。The present invention will be described below with reference to examples.
These embodiments are merely examples of the present invention, and the present invention is not limited to these embodiments.
【0031】(実施例1〜13)B液として、触媒化成
工業(株)製の商品名SI−350のシリカゾルを使用
した。表1に、このシリカゾルの特性を示す。A液に用
いられる粉末材料(粉体A)としては、表2に示すよう
な性状を有するものを使用した。なお、粉体Aの製造方
法は、早強セメントクリンカー微粉末100重量部、石
膏微粉末SO3換算で3重量部を混合粉砕した微粉末
(10.5μm通過分100容量%、2.2μm通過分4
0.5容量%)25重量部および高炉スラグ微粉末(1
0.5μm通過分100容量%、2.2μm通過分38.
4容量%)75重量部を混合して製造した。粒度測定は
レーザー式粒度分布測定装置(HELOS)を用いて行
った。(Examples 1 to 13) As the solution B, a silica sol having a trade name of SI-350 manufactured by KATAKASEI KOGYO CO., LTD. Was used. Table 1 shows the characteristics of the silica sol. As a powder material (powder A) used for the liquid A, one having properties as shown in Table 2 was used. The powder A is manufactured by mixing and pulverizing 100 parts by weight of the early-strength cement clinker fine powder and 3 parts by weight in terms of gypsum fine powder SO 3 (100 volume% for 10.5 μm passage, 2.2 μm passage Min 4
0.5 part by volume) and 25 parts by weight of blast furnace slag fine powder (1
100% by volume for 0.5 μm passage, 2.2 μm passage
(4% by volume) was mixed and produced. The particle size was measured using a laser type particle size distribution analyzer (HELOS).
【0032】さらに表3に示す基本配合において、A液
およびB液を調製し、さらにA液に表4に示す各種水和
抑制剤を表5の添加量で添加した。この添加量は、粉末
材料に対する重量%である。Further, in the basic formulation shown in Table 3, Liquid A and Liquid B were prepared, and various hydration inhibitors shown in Table 4 were added to Liquid A in the amounts shown in Table 5. This addition amount is% by weight based on the powder material.
【0033】表5に示すA液の練り置き時間(5、10
または30分間)で、A液およびB液を混合し、ゲルタ
イムを測定した。ゲルタイムは、カップ倒立法により測
定した。得られた結果を併せて表5に示す。The mixing time of the solution A shown in Table 5 (5, 10
Solution A and Solution B were mixed, and the gel time was measured. Gel time was measured by the cup inverted method. Table 5 also shows the obtained results.
【0034】[0034]
【表1】 [Table 1]
【0035】[0035]
【表2】 [Table 2]
【0036】[0036]
【表3】 [Table 3]
【0037】[0037]
【表4】 [Table 4]
【0038】[0038]
【表5】 [Table 5]
【0039】表5のゲルタイムの測定結果から、本発明
の地盤注入材は、従来のものに比較して、ゲルタイムの
長い緩結型の材料であることが判る。すなわち、水和抑
制剤を添加しない基本配合では、練り置き時間が30分
間であると、地盤注入材が瞬結するのに対し、本発明の
地盤注入材は、練り置き時間が30分間でも良好なゲル
タイムが得られている。From the measurement results of the gel time shown in Table 5, it can be seen that the ground injection material of the present invention is a loose-binding material having a longer gel time than the conventional one. That is, in the basic formulation without adding the hydration inhibitor, the ground injection material is instantaneously set when the mixing time is 30 minutes, whereas the ground injection material of the present invention is good even when the mixing time is 30 minutes. Gel time is obtained.
【0040】[0040]
【発明の効果】本発明によれば、懸濁型でかつ緩結型の
地盤注入材において、水硬性を有する粉体材料のスラリ
ーの練り置き時間が、ゲルタイム等の性能に影響を及ぼ
しにくい地盤注入材が提供される。According to the present invention, in a suspension-type and slow-setting type soil injection material, the mixing time of the slurry of the powdery material having hydraulic property is hardly affected by the performance such as the gel time. An injection material is provided.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI //(C04B 28/24 24:06) 103:20 ──────────────────────────────────────────────────続 き Continued on front page (51) Int.Cl. 6 Identification code FI // (C04B 28/24 24:06) 103: 20
Claims (3)
スラリーからなるA液と、シリカゾルおよび/または水
ガラスを主成分とするB液とからなる懸濁型の地盤注入
材であって、 前記A液に前記粉末材料の水和を抑制する水和抑制剤を
配合したことを特徴とする地盤注入材。1. A suspension type ground injection material comprising a liquid A composed mainly of a powdery material having hydraulic properties and a liquid B mainly composed of silica sol and / or water glass, A ground injection material, wherein a hydration inhibitor that suppresses hydration of the powder material is added to the liquid A.
ウ酸塩、オキシカルボン酸塩、ジカルボン酸類、ケトカ
ルボン酸類、糖アルコール類および糖類からなる群から
選択された少なくとも1種である請求項1に記載の地盤
注入材。2. The hydration inhibitor is at least one selected from the group consisting of fluorides, phosphates, borates, oxycarboxylates, dicarboxylic acids, ketocarboxylic acids, sugar alcohols and sugars. The ground injection material according to claim 1.
5〜10重量%の割合で配合される請求項1または2に
記載の地盤注入材。3. The method according to claim 1, wherein the hydration inhibitor is present in an amount of 0.0
The ground injection material according to claim 1 or 2, which is blended at a ratio of 5 to 10% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22658497A JPH1161126A (en) | 1997-08-22 | 1997-08-22 | Grouting material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22658497A JPH1161126A (en) | 1997-08-22 | 1997-08-22 | Grouting material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH1161126A true JPH1161126A (en) | 1999-03-05 |
Family
ID=16847474
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP22658497A Pending JPH1161126A (en) | 1997-08-22 | 1997-08-22 | Grouting material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH1161126A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001181633A (en) * | 1999-12-27 | 2001-07-03 | Tokuyama Corp | Grouting agent for inhibiting ground subsidence and method for inhibiting subsidence |
WO2005092990A1 (en) * | 2004-03-29 | 2005-10-06 | Robert Frederick Barber | Saccharide/cement coating compositions |
KR100746851B1 (en) | 2006-11-06 | 2007-08-07 | 주식회사 유산에이엔디 | Grout compositions containing functional nano composed inorganic power and grouting method of using it thereof |
KR100766626B1 (en) | 2005-12-22 | 2007-10-12 | 유겐가이샤 시모다기쥬쯔겐뀨죠 | Grout material |
JP2008007662A (en) * | 2006-06-30 | 2008-01-17 | Aichi Keiso Kogyo Kk | Soil hardening method |
JP2008223475A (en) * | 2004-07-20 | 2008-09-25 | Kyokado Eng Co Ltd | Grouting method |
AU2005225465B2 (en) * | 2004-03-29 | 2010-02-25 | Robert Frederick Barber | Saccharide/cement coating compositions |
EP1539652B1 (en) * | 2002-08-22 | 2010-06-23 | Akzo Nobel N.V. | Injection grouting |
-
1997
- 1997-08-22 JP JP22658497A patent/JPH1161126A/en active Pending
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001181633A (en) * | 1999-12-27 | 2001-07-03 | Tokuyama Corp | Grouting agent for inhibiting ground subsidence and method for inhibiting subsidence |
EP1539652B1 (en) * | 2002-08-22 | 2010-06-23 | Akzo Nobel N.V. | Injection grouting |
WO2005092990A1 (en) * | 2004-03-29 | 2005-10-06 | Robert Frederick Barber | Saccharide/cement coating compositions |
GB2427613A (en) * | 2004-03-29 | 2007-01-03 | Robert Frederick Barber | Saccharide/cement coating compositions |
GB2427613B (en) * | 2004-03-29 | 2008-02-27 | Robert Frederick Barber | Saccharide/cement coating compositions |
AU2005225465B2 (en) * | 2004-03-29 | 2010-02-25 | Robert Frederick Barber | Saccharide/cement coating compositions |
JP2008223475A (en) * | 2004-07-20 | 2008-09-25 | Kyokado Eng Co Ltd | Grouting method |
KR100766626B1 (en) | 2005-12-22 | 2007-10-12 | 유겐가이샤 시모다기쥬쯔겐뀨죠 | Grout material |
JP2008007662A (en) * | 2006-06-30 | 2008-01-17 | Aichi Keiso Kogyo Kk | Soil hardening method |
KR100746851B1 (en) | 2006-11-06 | 2007-08-07 | 주식회사 유산에이엔디 | Grout compositions containing functional nano composed inorganic power and grouting method of using it thereof |
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