JPH0248453A - Production of quick-setting concrete for covering concrete - Google Patents
Production of quick-setting concrete for covering concreteInfo
- Publication number
- JPH0248453A JPH0248453A JP63197192A JP19719288A JPH0248453A JP H0248453 A JPH0248453 A JP H0248453A JP 63197192 A JP63197192 A JP 63197192A JP 19719288 A JP19719288 A JP 19719288A JP H0248453 A JPH0248453 A JP H0248453A
- Authority
- JP
- Japan
- Prior art keywords
- concrete
- quick
- admixture
- setting
- setting agent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 49
- 238000000034 method Methods 0.000 claims abstract description 24
- 229920001577 copolymer Polymers 0.000 claims abstract description 10
- 239000000178 monomer Substances 0.000 claims abstract description 9
- 229920005646 polycarboxylate Polymers 0.000 claims description 15
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 125000000391 vinyl group Chemical class [H]C([*])=C([H])[H] 0.000 claims description 3
- 229920002554 vinyl polymer Polymers 0.000 claims description 3
- 239000004568 cement Substances 0.000 abstract description 17
- 230000000694 effects Effects 0.000 abstract description 15
- 239000002253 acid Substances 0.000 abstract description 6
- -1 carboxyl-substituted vinyl Chemical group 0.000 abstract description 3
- 238000010276 construction Methods 0.000 abstract description 3
- 239000011976 maleic acid Substances 0.000 abstract description 3
- 239000007787 solid Substances 0.000 abstract description 3
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 abstract description 2
- 239000002202 Polyethylene glycol Substances 0.000 abstract description 2
- 150000001336 alkenes Chemical class 0.000 abstract description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 abstract description 2
- 229920001223 polyethylene glycol Polymers 0.000 abstract description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 1
- 239000011796 hollow space material Substances 0.000 abstract 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 abstract 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 1
- 238000005507 spraying Methods 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 150000003839 salts Chemical class 0.000 description 15
- 238000012360 testing method Methods 0.000 description 12
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 10
- 229910052500 inorganic mineral Inorganic materials 0.000 description 9
- 239000011707 mineral Substances 0.000 description 9
- 235000010755 mineral Nutrition 0.000 description 9
- 239000000203 mixture Substances 0.000 description 7
- 239000000463 material Substances 0.000 description 6
- NVVZQXQBYZPMLJ-UHFFFAOYSA-N formaldehyde;naphthalene-1-sulfonic acid Chemical compound O=C.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 NVVZQXQBYZPMLJ-UHFFFAOYSA-N 0.000 description 5
- 239000004570 mortar (masonry) Substances 0.000 description 5
- 229920000877 Melamine resin Polymers 0.000 description 4
- 239000003638 chemical reducing agent Substances 0.000 description 4
- 238000009415 formwork Methods 0.000 description 4
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 4
- 238000003825 pressing Methods 0.000 description 4
- 229920001732 Lignosulfonate Polymers 0.000 description 3
- XFWJKVMFIVXPKK-UHFFFAOYSA-N calcium;oxido(oxo)alumane Chemical compound [Ca+2].[O-][Al]=O.[O-][Al]=O XFWJKVMFIVXPKK-UHFFFAOYSA-N 0.000 description 3
- 238000002788 crimping Methods 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 229910017053 inorganic salt Inorganic materials 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000004576 sand Substances 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 150000004645 aluminates Chemical class 0.000 description 2
- 230000003111 delayed effect Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 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
- UOZOCOQLYQNHII-UHFFFAOYSA-N 6-bromo-2-(6-bromo-3-hydroxy-1H-indol-2-yl)indol-3-one Chemical compound [O-]c1c([nH]c2cc(Br)ccc12)C1=[NH+]c2cc(Br)ccc2C1=O UOZOCOQLYQNHII-UHFFFAOYSA-N 0.000 description 1
- SPPBPJPDPYFSEQ-UHFFFAOYSA-N C(C=C/C(=O)O)(=O)O.C=CC1=CC=CC=C1.CC(C)=C Chemical compound C(C=C/C(=O)O)(=O)O.C=CC1=CC=CC=C1.CC(C)=C SPPBPJPDPYFSEQ-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- 239000011398 Portland cement Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- LFYJSSARVMHQJB-QIXNEVBVSA-N bakuchiol Chemical compound CC(C)=CCC[C@@](C)(C=C)\C=C\C1=CC=C(O)C=C1 LFYJSSARVMHQJB-QIXNEVBVSA-N 0.000 description 1
- 238000009412 basement excavation Methods 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 229910001634 calcium fluoride Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 239000000176 sodium gluconate Substances 0.000 description 1
- 229940005574 sodium gluconate Drugs 0.000 description 1
- 235000012207 sodium gluconate Nutrition 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 239000000126 substance Substances 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
- 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
- C04B24/2641—Polyacrylates; Polymethacrylates
- C04B24/2647—Polyacrylates; Polymethacrylates containing polyether side chains
-
- 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
-
- 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
- C04B24/2664—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of ethylenically unsaturated dicarboxylic acid polymers, e.g. maleic anhydride copolymers
-
- 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
- C04B24/2688—Copolymers containing at least three different monomers
-
- 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
- C04B24/28—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C04B24/32—Polyethers, e.g. alkylphenol polyglycolether
-
- 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
- C04B28/02—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 hydraulic cements other than calcium sulfates
-
- 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
- C04B2111/00034—Physico-chemical characteristics of the mixtures
- C04B2111/00146—Sprayable or pumpable mixtures
- C04B2111/00155—Sprayable, i.e. concrete-like, materials able to be shaped by spraying instead of by casting, e.g. gunite
-
- 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
- C04B2111/00482—Coating or impregnation materials
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)
- Inorganic Chemistry (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は急結剤を用いる覆工コンクリート用の急結コン
クリートの製造方法に関するものであり、長時間にわた
り、コンクリートの流動性を保持しておいた後に、短時
間で急結させることのできるコンクリートの製造方法に
関するものである。[Detailed Description of the Invention] (Industrial Application Field) The present invention relates to a method for producing quick-setting concrete for lining concrete using a quick-setting agent, which maintains the fluidity of concrete for a long period of time. The present invention relates to a method for producing concrete that can be quickly set in a short period of time after being set.
(背景技術)
トンネルまたは地下空洞の掘削面へのコンクリートの施
工方法として急結剤を添加して施工するコンクリートの
覆工工法が用いられていることは周知のことである。こ
の工法には大別すると2つの方法があげられる。その1
つは、水を用いず空練りされたコンクリートあるいは予
め水を加えて練り混ぜられたコンクリートを空気流搬送
してノズルの直近で急結剤を添加してノズルから吹き出
して施工する吹き付は工法であり、他の1つは、予め練
り混ぜられたコンクリートを掘削面に設けられた型枠内
に流し込み、これを押し付ける、押し付は工法あるいは
圧着工法と呼ばれる方法である。さらに、上記の吹き付
は工法は湿式吹き付は方式と乾式吹き付は方式に大別さ
れる。この乾式吹き付は方式とは、空練りコンクリート
を輸送ホース中を空気流搬送し、ノズルの口から吹き出
して施工する方式で、水はノズルの口の直近の位置で輸
送ホース内に加えられる。この方式は添加水量のコント
ロールが難しくコンクリートの物性を支配する最も重要
な因子である水セメント比(以下W/Cと略する)の管
理が難しいこと、および粉塵の発生が多く作業環境を悪
化させることが難点とされている。また、上記の湿式吹
き付は方式とは予め練り混ぜられたコンクリートを輸送
ホース中を空気流搬送してノズルの口から吹き出して施
工する方式(輸送ホースの途中までポンプ輸送し以後空
気流搬送する場合もある)である。この方式はW/Cの
管理が容易で粉塵の発生が少ない利点があるのでかなり
広〈実施されるようになってきている。両方式における
急結剤の添加は、乾式吹き付は方式の場合には、コンク
リートの空練り時またはノズルの口付近であるが、湿式
吹き付は方式の場合には、ノズルの口の近くで添加され
る。また、前記の押し付は工法あるいは圧着工法は予め
練り混ぜられたコンクリートを空気流搬送せずポンプ圧
送してノズルの口付近で急結剤を添加し、急結剤を添加
したコンクリートを掘削面に設けられた型枠内に流し込
む工法であるか、この工法の場合、コンクリートは型枠
内に流し込まれた後硬化する直前まで、すなわち急結剤
添加後、数分間は流動性に富み(コンクリートの柔らか
さを判定する尺度であるスランプ値で18cm程度)そ
の後、作業能率を高めるために早急に型枠を脱型し、次
の工程に移る関係上3〜5分でl kgf/ cm”の
圧縮強度が得られる程度にまで硬化することが必要であ
る。(Background Art) It is well known that a concrete lining method in which a quick-setting agent is added is used as a method for constructing concrete on the excavated surface of a tunnel or underground cavity. This construction method can be roughly divided into two types. Part 1
One is the spraying method, in which concrete is mixed in the air without using water, or concrete is mixed in advance with water, conveyed by an air stream, a quick-setting agent is added in the vicinity of the nozzle, and the mixture is sprayed out of the nozzle. The other method is to pour pre-mixed concrete into a form provided on the excavation surface and press it against the concrete, which is called the pressing method or crimping method. Furthermore, the above-mentioned spraying method is roughly divided into wet spraying method and dry spraying method. This dry spraying method is a method in which dry-mixed concrete is carried by air flow through a transport hose and sprayed from the mouth of a nozzle, and water is added into the transport hose at a position immediately adjacent to the mouth of the nozzle. With this method, it is difficult to control the amount of water added, and the water-cement ratio (hereinafter abbreviated as W/C), which is the most important factor governing the physical properties of concrete, is difficult to control, and a lot of dust is generated, deteriorating the working environment. This is considered to be a difficult point. In addition, the above-mentioned wet spraying method is a method in which pre-mixed concrete is conveyed by air flow through a transport hose and then blown out from the mouth of the nozzle. ). This method has the advantages of easy W/C management and less generation of dust, so it has become quite widely practiced. In both methods, the quick-setting agent is added when dry mixing the concrete or near the nozzle mouth in the dry spraying method, but it is added near the nozzle mouth in the wet spraying method. added. In addition, the above-mentioned pressing method or crimping method involves pumping pre-mixed concrete without conveying air flow, adding an quick-setting agent near the mouth of the nozzle, and applying the quick-setting agent to the excavated surface. In this method, the concrete remains highly fluid for several minutes after being poured into the formwork until just before it hardens, i.e. after adding the quick setting agent. The slump value, which is a measure of the softness of the material, is approximately 18 cm).Then, in order to increase work efficiency, the formwork is removed immediately, and in order to move on to the next process, the 1 kgf/cm" It is necessary to harden to the extent that compressive strength is obtained.
ここで言う急結剤とは、JIS A 0203 rコン
クリート用語」において「セメントの水利反応を早め、
凝結時間を著しく短くするために用いる混和剤」として
定義付けられているものであり、代表的なものとしては
アルミン酸アルカリおよび炭酸アルカリの単味または両
者の混合物である無機塩系(粉体および液状)のもの、
セメント鉱物系、天然鉱物系、水ガラス系およびカルシ
ウムサルホアルミ不−ト系等、種々のものがある。ここ
で、無機塩系急結剤とはアルミン酸塩、または/および
炭酸塩からなる急結剤で、天然鉱物系急結剤とは仮焼間
ばん石に、炭酸塩または/およびアルミン酸塩等を配合
したもので、セメント鉱物系急結剤とはCa0−AQ2
01.12cao’7ALOx、CaO・2AQ201
.1lCaO・7AQ20.・CaF2.3Ca()3
A(220,・CaF2等のカルシウムアルミネートお
よびこれらの無定形物を主体とするセメント質のもので
あって、これにさらに石膏類や無機塩系急結剤を配合し
たものも含まれる。The term “accelerating agent” mentioned here is defined in JIS A 0203 r Concrete Terminology as “accelerating the water use reaction of cement.
It is defined as an admixture used to significantly shorten the setting time, and typical examples include inorganic salts (powder and liquid),
There are various types such as cement mineral type, natural mineral type, water glass type and calcium sulfo aluminum inert type. Here, the inorganic salt-based quick-setting agent is a quick-setting agent consisting of aluminate and/or carbonate, and the natural mineral-based quick-setting agent is a quick-setting agent made of aluminate and/or carbonate. Cement mineral quick setting agent is Ca0-AQ2.
01.12cao'7ALOx, CaO・2AQ201
.. 1lCaO・7AQ20.・CaF2.3Ca()3
A(220, CaF2 and other calcium aluminates) and cementitious materials that are mainly composed of these amorphous materials, and also include those containing gypsum or inorganic salt-based quick-setting agents.
これら急結剤の添加量は、コンクリート中のセメン11
1に対する添加重量%(使用量という)で表して、無機
塩系の場合は約2〜8%(粉体及び液状量)、セメント
鉱物系の場合は約5〜lO%、天然鉱物系の場合は約4
〜10%である。この使用量は通常の混和剤の使用量が
固形物換算で1%程度以下であるのに比べると多い。The amount of these quick-setting agents added is the cement 11 in concrete.
Expressed in weight percent (referred to as usage amount) added to 1, it is approximately 2 to 8% (powder and liquid amount) for inorganic salts, approximately 5 to 10% for cement minerals, and approximately 5 to 10% for natural minerals. is about 4
~10%. This usage amount is large compared to the usage amount of ordinary admixtures, which is about 1% or less in terms of solids.
この急結剤は、コンクリートに用いられる主要材料であ
るセメント、砂、砂利に比べて高価であり、所要の急結
効果を得るための急結剤の使用量は一般の混和剤に比べ
て多く、覆工コンクリート中に占めるコスト割合は大き
い。従って、なるべく少ない使用量で所要の急結効果を
達成することが望ましい。This quick-setting agent is more expensive than cement, sand, and gravel, which are the main materials used in concrete, and the amount of quick-setting agent used to achieve the desired quick-setting effect is larger than that of ordinary admixtures. , the cost ratio in lining concrete is large. Therefore, it is desirable to achieve the desired rapid setting effect with as little amount as possible.
また、湿式吹き付は方式においては、乾式吹き付は方式
の場合に比べて急結効果が小さくなる。その原因の1つ
は、セメント粒子が急結剤と接触する前に既に水と接触
しているので、その表面に初期水和物の薄層が形成され
ていて、これがセメント粒子と急結剤との接触に対して
抵抗となることである(特開昭61−31572号参照
)。もう一つの原因は湿式吹き付は方式の場合W/Cが
大きくなることである。すなわち、乾式吹き付は方式で
は約45%程度であるのに対し湿式吹き付は方式では5
5%以上である。急結効果はW/Cの大小によって鋭敏
に影響を受け、W/Cの大きいほど急結効果は小さくな
るものであるが、湿式吹き付は方式の場合、輸送ホース
内のコンクリートの搬送を円滑に進行させるためにコン
クリートの軟度をかなり大きくしなければならず、従っ
てW/Cも大きくせざるを得ない。同様に、押し付は工
法ならびに圧着工法の場合にも型枠内にコンクリートを
充填性良く流し込む関係上コンクリートの軟度をかなり
大きくしなければならないが、W/Cを大きくしたので
は急結性が劣るという問題が生ずる。In addition, wet spraying has a smaller rapid setting effect than dry spraying. One of the reasons for this is that before the cement particles come into contact with the quick-setting agent, they have already come into contact with water, so a thin layer of initial hydrate is formed on the surface of the cement particles. (See Japanese Unexamined Patent Publication No. 31572/1983). Another reason is that the W/C becomes large when using the wet spraying method. In other words, dry spraying is about 45%, while wet spraying is about 5%.
It is 5% or more. The rapid setting effect is sensitively affected by the size of the W/C, and the larger the W/C, the smaller the rapid setting effect, but when wet spraying is used, concrete can be transported smoothly in the transport hose. The softness of the concrete must be considerably increased in order for the concrete to proceed, and therefore the W/C must also be increased. Similarly, in the case of the pressing method and the crimping method, the softness of the concrete must be considerably increased in order to pour the concrete into the formwork with good filling properties, but increasing the W/C will cause rapid setting. The problem arises that the quality is inferior.
(発明の開示)
本発明者らはトンネルまたは地下空洞の掘削面に、予め
練り混ぜたコンクリートに急結剤を添加して施工するコ
ンクリートの覆工工法において、覆工コンクリートにお
ける急結剤の急結効果を、コンクリートの流動性を損な
わずに増大させる手段の提供を目的として鋭意研究を行
ったところ、予め練り混ぜるコンクリートに分子構造の
一部にカルボキシル基置換ビニルモノマーを含む共重合
体を主成分とするポリカルボン酸塩系混和剤を添加し、
そのコンクリートに急結剤を添加することにより、この
目的を達成することができた。(Disclosure of the Invention) The present inventors have developed a concrete lining method in which a quick-setting agent is added to pre-mixed concrete on the excavated surface of a tunnel or underground cavity. We conducted extensive research with the aim of providing a means to increase the concrete's concrete fluidity without impairing its fluidity, and found that a copolymer containing a carboxyl group-substituted vinyl monomer as part of its molecular structure was added to the pre-mixed concrete. Add the polycarboxylate admixture as an ingredient,
By adding an accelerating agent to the concrete, this objective could be achieved.
すなわち、本発明は、トンネルまたは地下空洞の掘削面
に、予め練り混ぜたコンクリートにあとから急結剤を添
加して施工するコンクリートの覆工工法において、予め
練り混ぜるコンクリートに対して、ポリカルボン酸塩系
混和剤を添加することを特徴とする覆工コンクリートの
製造方法を提供するものである。That is, the present invention provides a concrete lining method in which an accelerating agent is added to pre-mixed concrete on the excavated surface of a tunnel or underground cavity, and in which polycarboxylic acid is added to the pre-mixed concrete. The present invention provides a method for producing lining concrete, which is characterized by adding a salt-based admixture.
ここにいう急結剤についてはさきに述べたとおりである
。上記のポリカルボン酸塩系混和剤とはポリカルボン酸
塩系物質そのものまたはこれを減水剤成分として配合し
ている混和剤のことであって、通常ポリカルボン酸塩系
混和剤は、JIS A 0203 rコンクリート用語
」に定めるところの「減水剤」として用いられているも
のである。通常、コンクリートに朋いられている混和剤
の減水剤成分としてはリグニンスルホン酸塩及びその誘
導体、オキシカルボン酸塩、ナフタリンスルホン酸ホル
マリン縮金物塩、メラミンスルホン酸ホルマリン縮金物
塩、およびポリカルボン酸塩系等があるが、本発明の方
法においてはポリカルボン酸塩系のものが特に好ましく
使用される。本発明の方法において使用するポリカルボ
ン酸塩系混和剤とは、カルボキシル基置換ビニルモノマ
ーを一成分として含む共重合体を含む混和剤を指す。具
体的な例としては、ポリカルボンM塩基混和剤には水溶
性の、σ。The quick setting agent referred to here is as described above. The above-mentioned polycarboxylate-based admixture refers to a polycarboxylate-based substance itself or an admixture containing this as a water reducing agent component, and polycarboxylate-based admixtures are usually compliant with JIS A 0203. It is used as a ``water reducing agent'' as defined in ``Concrete Terminology''. The water-reducing agent components of admixtures usually used in concrete include lignin sulfonates and their derivatives, oxycarboxylate salts, naphthalene sulfonate formalin condensate salts, melamine sulfonate formalin condensate salts, and polycarboxylic acids. Although there are salt-based ones, polycarboxylate-based ones are particularly preferably used in the method of the present invention. The polycarboxylate-based admixture used in the method of the present invention refers to an admixture containing a copolymer containing a carboxyl group-substituted vinyl monomer as one component. As a specific example, the polycarboxylic M base admixture has a water-soluble σ.
β−不飽和ジカルボン酸とオレフィンの共重合体、ポリ
エチレングリコールモノアリルエーテルとマレイン酸系
単量体及びこれらと共重合可能な単量体から導かれる共
重合体、イソブチレン−スチレンマレイン酸系、インブ
チレン−アクリル酸エステル−マレイン酸系、インブチ
レン−スチレン−アクリル酸エステル−マレイン酸系の
各共重合体等があげられる。Copolymers of β-unsaturated dicarboxylic acids and olefins, copolymers derived from polyethylene glycol monoallyl ether and maleic monomers, and monomers copolymerizable with these, isobutylene-styrene maleic acid monomers, Examples include copolymers of butylene-acrylic ester-maleic acid and inbutylene-styrene-acrylic ester-maleic acid.
本発明の方法に用いるポリカルボン酸塩系混和剤の使用
量は、セメント重量に対し固形物換算で0.01%〜0
.5%、好ましくは0.03%〜0.2%の使用量範囲
が適当である。同一コンシステンシーのコンクリートで
急結剤の使用量は同一として試験した場合、ポリカルボ
ン酸塩系混和剤の使用量がこれ以下の場合には満足すべ
き急結効果が得られない。使用量増大と共に急結効果は
大きくなるが上記上限値を越える使用量では頭打現象が
現れて経済的でない。The amount of the polycarboxylate admixture used in the method of the present invention is 0.01% to 0.0% in terms of solids based on the weight of cement.
.. A usage range of 5%, preferably 0.03% to 0.2% is suitable. When testing concrete with the same consistency and using the same amount of quick setting agent, if the amount of polycarboxylate admixture used is less than this, a satisfactory quick setting effect cannot be obtained. As the amount used increases, the rapid setting effect increases, but if the amount used exceeds the above-mentioned upper limit, a plateauing phenomenon will occur, making it uneconomical.
湿式吹き付は工法に供されるコンクリートは、通常打設
されるコンクリートに比べて全骨材中に占める細骨材の
割合(s/a)が大きく、リグニンスルホン酸塩あるい
はオキシカルボン酸塩系等の混和剤ではこの剤の通常の
使用量範囲では減水効果が小さく、減水効果を上げよう
として、この剤の使用量を増加させると、コンクリート
の凝結硬化が遅延され、併用する急結剤の効果を阻害す
るために吹き付は工法に使用するには適当でない。また
、湿式吹き付は方式とはさきに述べた如く、予め混練り
されたコンクリートにノズルの口付近で急結剤を添加し
て吹き付ける工法であり、コンクリートは練り混ぜられ
たあと吹き付けられるまで1〜2時間時間線り置かれる
ことが多く、その間に流動性が低下するという問題が生
ずる。ナフタレンスルホン酸ホルマリン縮金物塩系およ
びメラミンスルホン酸ホルマリン縮金物塩系の混和剤は
、減水効果にすぐれ、使用量を増加させても、大きな凝
結硬化遅延性を示すことなく高い流動性を確保できる混
和剤であるが、これらの混和剤は、減水効果の持続時間
が短く、混和剤を添加して20〜30分後にはコンクリ
ートの流動性が大幅に小さくなり、いわゆるスランプロ
スが大きいという欠点を有するので本発明方法において
はこれらの剤を減水剤として単独で用いることは適当で
ない。押し付は工法あるいは圧着工法においてはコンク
リートを型枠内に密実に充填する必要上、2時間程度は
流動性を保つことが必要であるので、同様にスランプロ
スの大きい混和剤を用いることは適当でない。さらに、
ナフタレンスルホン酸ホルマリン縮合物塩系の混和剤は
、3CaO・AQxOx、4CaO・AQ、03・Fe
、O,等のカルシウムアルミネート系の鉱物に異常に多
く吸着することが知られている(セメント技術年報35
゜P2O2参照)。現在、急結剤においてはその初期強
度発現性(急結硬化発現性)、対湧水性等の点からセメ
ント鉱物系が湿式吹き付は用急結剤として主流になりつ
つあるが、このものは先に述べた如くカルシウムアルミ
ネートを主成分とするものであり、ナフタレンスルホン
酸ホルマリン縮合物塩系の混和剤と混合された場合カル
シウムアルミネート表面への吸着が多くなり、急結効果
が阻害される。The concrete used in the wet spraying method has a larger proportion (s/a) of fine aggregate in the total aggregate compared to normally poured concrete, and contains lignin sulfonate or oxycarboxylate-based concrete. With admixtures such as, the water reduction effect is small in the range of normal usage of this agent, and if the usage of this agent is increased in an attempt to increase the water reduction effect, setting and hardening of concrete will be delayed, and the rapid setting agent used in combination will be delayed. Spraying is not suitable for use in construction methods as it inhibits the effectiveness. As mentioned above, wet spraying is a method in which a quick setting agent is added to pre-mixed concrete near the mouth of the nozzle and then sprayed. It is often left to stand for up to 2 hours, during which time a problem arises in that the fluidity decreases. Admixtures based on naphthalene sulfonic acid formalin condensate salts and melamine sulfonate formalin condensate salts have an excellent water-reducing effect, and even if the amount used is increased, high fluidity can be ensured without showing a large retardation of setting and hardening. However, these admixtures have the disadvantage that their water-reducing effect lasts only a short time, and the fluidity of concrete decreases significantly 20 to 30 minutes after adding the admixture, resulting in a large slump loss. Therefore, it is not appropriate to use these agents alone as water reducing agents in the method of the present invention. In the pressing method or the pressure bonding method, it is necessary to densely fill the concrete into the formwork, and it is necessary to maintain fluidity for about 2 hours, so it is also appropriate to use an admixture with a large slump loss. Not. moreover,
Naphthalene sulfonic acid formalin condensate salt admixtures include 3CaO・AQxOx, 4CaO・AQ, 03・Fe
It is known that abnormally large amounts of calcium aluminate minerals such as , O, etc. are adsorbed (Cement Technology Annual Report 35
゜See P2O2). Currently, cement mineral-based quick-setting agents are becoming mainstream as quick-setting agents for wet spraying due to their initial strength development (rapid setting and hardening development) and resistance to spring water. As mentioned above, calcium aluminate is the main component, and when mixed with a naphthalene sulfonic acid formalin condensate salt admixture, more adsorption occurs on the surface of calcium aluminate, inhibiting the rapid setting effect. Ru.
本発明者らはこのような状況に鑑み鋭意検討した結果、
上記のとおり、ポリカルボン酸塩系の混和剤を予め練り
混ぜるコンクリートに使用することにより、トンネルま
たは地下空洞の掘削面に、予め練り混ぜたコンクリート
にあとから急結剤を添加して施工するコンクリートの覆
工工法において、コンクリートにおける急結剤の急結効
果を、コンクリートの流動性を損なわずに増大させ得る
ことに成功したものである。As a result of intensive study in view of this situation, the inventors of the present invention found that
As mentioned above, by using polycarboxylate-based admixtures in pre-mixed concrete, concrete can be constructed on the excavated surface of tunnels or underground cavities by adding quick-setting agents to the pre-mixed concrete. In this lining method, we succeeded in increasing the quick-setting effect of the quick-setting agent on concrete without impairing the fluidity of the concrete.
以下に、本発明の実施例を掲げ、本発明をさらに具体的
に説明する。EXAMPLES Below, the present invention will be described in more detail with reference to Examples.
実施例 1
本例により、覆工コンクリートのモデル試験として所定
の配合でコンクリートを練り混ぜた後、ウニ゛ントスク
リーニング(7ルイの目が5mmのフルイを用いモルタ
ル部分と粗骨材部分とをふるい分けること)によりモル
タルを分離し、得られたモルタルに急結剤を添加して上
記のポリカルボン酸塩系混和剤の添加効果を確認するこ
とができる。Example 1 According to this example, as a model test for lining concrete, concrete was mixed in a predetermined proportion, and then unit screening (using a 5 mm sieve with 7 Louis meshes was used to sieve the mortar part and the coarse aggregate part). The effect of adding the above-mentioned polycarboxylate admixture can be confirmed by separating the mortar and adding an accelerating agent to the obtained mortar.
(1)コンクリートの材料
(イ)セメント:小野田、三菱、住人社製普通ポルトラ
ンドセメントを等量
混合して使用。(1) Concrete materials (a) Cement: Use a mixture of equal amounts of ordinary Portland cement manufactured by Onoda, Mitsubishi, and Juminsha.
(ロ)粗骨材:青梅産硬質砂岩砕石(比重=2.64、
吸水率−0,67%、F、M= 6.35、MS−15
mm)
(ハ)細骨材:大井用水系産陸砂と千葉産山砂を混合し
て使用(比重=
2.65、吸水率−1,34%、FM=2.69)
(ニ)混和剤:
a)ポリカルボン酸系混和剤
ポリアルキレングリコールモノメタアクリル酸エステル
とメタアクリル酸の共重合物(略号A:日曹マスタービ
ルダーズ(株)製)
b) リグニンスルホン酸塩系混和剤
商品名:ホゾリスNo、8 (略号B:日曹マスタービ
ルダーズ(株)製)
C)オキシカルボン酸塩系混和剤
グルコン酸ナトリウム(略号C:試薬)d) ナフタ
レンスルホン酸ホルマリン縮合物塩系混和剤
商品名:マイティー150(略号D:花王(株)製)
e)メラミンスルホン酸ホルマリン縮金物塩系混和剤
商品名: NL−4000(略号E:日曹マスタービル
ダーズ(株)製)
混和剤の使用量は混和剤を用いないプレーンコンクリー
トと配合に示した水量で同一のコンシスチンシーの得ら
れる使用量とし、セメント重量に対する重量%で示した
。(b) Coarse aggregate: crushed hard sandstone from Ome (specific gravity = 2.64,
Water absorption rate -0.67%, F, M = 6.35, MS-15
mm) (c) Fine aggregate: Use a mixture of land sand from the Oi water system and mountain sand from Chiba (specific gravity = 2.65, water absorption -1.34%, FM = 2.69) (d) Admixture : a) Polycarboxylic acid admixture Copolymer of polyalkylene glycol monomethacrylic acid ester and methacrylic acid (abbreviation A: manufactured by Nisso Master Builders Co., Ltd.) b) Lignosulfonate admixture Product name: Hozolith No. 8 (abbreviation B: manufactured by Nisso Master Builders Co., Ltd.) C) Oxycarboxylate-based admixture Sodium gluconate (abbreviation C: reagent) d) Naphthalenesulfonic acid formalin condensate salt-based admixture Product name: Mighty 150 (abbreviation D: manufactured by Kao Corporation) e) Melamine sulfonic acid formalin condensate salt admixture Product name: NL-4000 (abbreviation E: manufactured by Nisso Master Builders Co., Ltd.) The amount of admixture used is The amount of water used to obtain the same consistency as that of plain concrete without additives and the amount of water shown in the formulation is expressed in weight % based on the weight of cement.
(ネ)急結剤:
r)無機塩系粉体急結剤
商品名: QP−500(略号F:日曹マスタービルダ
ーズ(株)製)
g)セメント鉱物系急結剤
商品名: QP−55(略号G:日曹マスタービルダー
ズ(株)製)
急結剤の使用量はそれぞれメーカーの推奨する標準的な
使用量とし、セメント重量に対する重量%で示した。(ne) Quick setting agent: r) Inorganic salt powder quick setting agent brand name: QP-500 (abbreviation F: manufactured by Nisso Master Builders Co., Ltd.) g) Cement mineral quick setting agent brand name: QP-55 (Abbreviation G: Manufactured by Nisso Master Builders Co., Ltd.) The usage amount of the quick-setting agent was the standard usage amount recommended by each manufacturer, and was expressed in weight % with respect to the cement weight.
(2)コンクリートの配合 コンクリートの配合は第1表に示したとおりである。(2) Concrete mix The mix of concrete is as shown in Table 1.
(3)試 験
コンクリートを練り混ぜた後5mmフルイを用いてモル
タル部分と粗骨材を分離して得られたモルタルを30分
間練り置き、これに急結剤を加えて20秒間手練りする
。このものにつきJIS A6204 rコンクリート
用化学混和剤」の附属書1コンクリートの凝結時間試験
方法に準拠して凝結の始発時間(貫入抵抗が35kgf
/ crrr2に達する時間)を測定した。なお、凝結
時間は急結剤を添加してからの時間(分−秒)である。(3) After mixing the test concrete, separate the mortar and coarse aggregate using a 5 mm sieve, knead the resulting mortar for 30 minutes, add an quick-setting agent, and knead by hand for 20 seconds. Regarding this product, the initial setting time (penetration resistance of 35 kgf
/crrr2) was measured. Note that the setting time is the time (minutes-seconds) after adding the quick-setting agent.
(4)試験結果
急結剤Fを使用したときの試験結果は第2表に示すとお
りであり、急結剤Gを使用したときの試験結果は第3表
に示すとおりである。急結剤Fを用い混和剤を使用しな
い場合においては、20分経過しても始発には達しなか
ったが、ポリカルボン酸塩系混和剤(略号A)を使用す
ることにより13分40秒で始発に達していることが判
る。他の混和剤では、混和剤Eが、17分20秒で始発
に達しているほかは、すべて20分経過しても始発には
達しなかった。さらに、急結剤Bを使用した場合でも、
ポリカルボン酸塩系混和剤(略号A)を使用することに
より1分以内で始発に達しており、同−急結剤量で凝結
時間が大幅に短縮されていることが判る。(4) Test results The test results when using quick setting agent F are as shown in Table 2, and the test results when using quick setting agent G are as shown in Table 3. In the case of using quick setting agent F and no admixture, the initial stage was not reached even after 20 minutes, but by using polycarboxylate admixture (abbreviation A), it was achieved in 13 minutes and 40 seconds. It can be seen that the starting point has been reached. All of the other admixtures did not reach the initial stage even after 20 minutes had passed, except for the admixture E, which reached the initial stage in 17 minutes and 20 seconds. Furthermore, even when using quick setting agent B,
By using the polycarboxylate admixture (abbreviation A), the initial stage was reached within 1 minute, and it can be seen that the setting time was significantly shortened with the same amount of quick setting agent.
第3表 凝結時間の測定結果(急結剤G)実施例 2
本例により、急結剤を添加するまでのコンクリートの流
動性が、どのくらい保持できるのか、が示される。Table 3 Measurement results of setting time (accelerating agent G) Example 2 This example shows how long the fluidity of concrete can be maintained until the accelerating agent is added.
試験に使用した材料、ならびにコンクリートの配合は実
施例11比較例1,4.5と同一である。なお、本試験
に用いた混和剤はポリカルボン酸塩系混和剤(略号A)
、ナフタレンスルホン酸ホルマリン縮金物塩系混和剤(
略号D)、メラミンスルホン酸ホルマリン縮金物塩系混
和剤(略号E)である。The materials used in the test and the concrete mix were the same as in Example 11 and Comparative Examples 1 and 4.5. The admixture used in this test was a polycarboxylate admixture (abbreviation A).
, naphthalene sulfonic acid formalin condensate salt admixture (
Abbreviation D) and melamine sulfonic acid formalin condensate salt admixture (abbreviation E).
(1)試験
可傾式ミキサーでコンクリートを練り混ぜたのち、コン
クリート全量を排出しスランプの測定を行った。次にコ
ンクリート全量をミキサーに戻し、低速(2rpm)で
所定時間ミキサーの回転を続け30分後、60分後にス
ランプの測定を行った。(1) Test After mixing concrete with a tilting mixer, the entire amount of concrete was discharged and slump was measured. Next, the entire amount of concrete was returned to the mixer, and the mixer was continued to rotate at a low speed (2 rpm) for a predetermined period of time, and slump was measured after 30 minutes and 60 minutes.
(2)試験結果
試験結果を第4表に示す。これより、ポリカルボン酸塩
系混和剤(略号C)を使用したコンクリ・−トのスラン
プは長時間経過しても他のものに比較して低下しないこ
とが判る。混和剤Gを用いた場合、凝結時間が比較的早
かったが、スランプの経時変化が太きく60分後には5
cm以下となることが判る。(2) Test results The test results are shown in Table 4. From this, it can be seen that the slump of concrete using the polycarboxylate admixture (abbreviation C) does not decrease compared to other types even after a long period of time. When Admixture G was used, the setting time was relatively quick, but the slump changed rapidly over time, and after 60 minutes it was 5.
It turns out that it is less than cm.
第4表 コンクリートのスランプロス試験結果て作業効
率を高めることができるので、産業上の利用価値は極め
て大きい。Table 4 Results of concrete slump loss test As work efficiency can be improved, the industrial value is extremely high.
Claims (1)
ンクリートに急結剤を添加して施工するコンクリートの
覆工工法において、予め練り混ぜるコンクリートに対し
て分子構造の一部にカルボキシル基置換ビニルモノマー
を含む共重合体を主成分とするポリカルボン酸塩系混和
剤を添加することを特徴とするコンクリートの製造方法
。In the concrete lining method, in which a quick setting agent is added to pre-mixed concrete on the excavated surface of a tunnel or underground cavity, a carboxyl group-substituted vinyl monomer is added to part of the molecular structure of the pre-mixed concrete. A method for producing concrete, which comprises adding a polycarboxylate admixture whose main component is a copolymer containing:
Priority Applications (14)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63197192A JPH0248453A (en) | 1988-08-09 | 1988-08-09 | Production of quick-setting concrete for covering concrete |
DE3925306A DE3925306A1 (en) | 1988-08-09 | 1989-07-31 | ACCELERATOR FOR SPRAY CONCRETE |
CH2898/89A CH678620A5 (en) | 1988-08-09 | 1989-08-04 | |
AU39401/89A AU622467B2 (en) | 1988-08-09 | 1989-08-07 | Cement compositions |
GB8918019A GB2221673B (en) | 1988-08-09 | 1989-08-07 | Quick setting concrete compositions for use as lining construction concrete |
AT0189889A ATA189889A (en) | 1988-08-09 | 1989-08-08 | ACCELERATOR FOR SPRAY CONCRETE |
ES8902820A ES2018382A6 (en) | 1988-08-09 | 1989-08-08 | Quick setting concrete compositions for use as lining construction concrete |
IT8921478A IT1231777B (en) | 1988-08-09 | 1989-08-08 | QUICK-SETTING CONCRETE COMPOSITIONS FOR USE AS CONCRETE FOR INTERIOR COATING CONSTRUCTION. |
FR8910686A FR2635320B1 (en) | 1988-08-09 | 1989-08-08 | QUICK SET CONCRETE COMPOSITIONS FOR COATING CONCRETE |
BR898903983A BR8903983A (en) | 1988-08-09 | 1989-08-08 | CEMENT COMPOSITION AND PROCESS FOR THE PRODUCTION AND APPLICATION OF THE SAME |
CA000607887A CA1337871C (en) | 1988-08-09 | 1989-08-09 | Quick setting concrete compositions for use as lining construction concrete |
BE8900855A BE1003765A5 (en) | 1988-08-09 | 1989-08-09 | Compositions for rapid concrete coating of concrete. |
SG143594A SG143594G (en) | 1988-08-09 | 1994-10-05 | Quick setting concrete compositions for use as lining construction concrete |
HK134194A HK134194A (en) | 1988-08-09 | 1994-12-01 | Quick setting concrete compositions for use as lining construction concrete |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63197192A JPH0248453A (en) | 1988-08-09 | 1988-08-09 | Production of quick-setting concrete for covering concrete |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0248453A true JPH0248453A (en) | 1990-02-19 |
JPH0553743B2 JPH0553743B2 (en) | 1993-08-10 |
Family
ID=16370340
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63197192A Granted JPH0248453A (en) | 1988-08-09 | 1988-08-09 | Production of quick-setting concrete for covering concrete |
Country Status (13)
Country | Link |
---|---|
JP (1) | JPH0248453A (en) |
AT (1) | ATA189889A (en) |
AU (1) | AU622467B2 (en) |
BE (1) | BE1003765A5 (en) |
BR (1) | BR8903983A (en) |
CA (1) | CA1337871C (en) |
CH (1) | CH678620A5 (en) |
DE (1) | DE3925306A1 (en) |
ES (1) | ES2018382A6 (en) |
FR (1) | FR2635320B1 (en) |
GB (1) | GB2221673B (en) |
HK (1) | HK134194A (en) |
IT (1) | IT1231777B (en) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2659895A1 (en) * | 1990-03-22 | 1991-09-27 | Nouvion Bernard | Process for the manufacture of materials made of stabilised, compressed and crystallised soil aggregates and the product obtained |
NO172255C (en) * | 1991-01-08 | 1993-06-23 | Sandoz Ltd | PROCEDURE FOR MIXING ADDITIVES IN A SUBSTANCES AND ADDITION TO USE BY THE PROCEDURE |
DE4217181A1 (en) * | 1992-05-23 | 1993-11-25 | Chemie Linz Deutschland | Melamine glyoxylic acid or salt condensate use in hydraulic binder - to increase flow, retard setting and opt. increase strength of set prod. |
CH686780A5 (en) * | 1992-07-22 | 1996-06-28 | Sandoz Ag | Fliessfaehige cement mixtures. |
AT399340B (en) * | 1993-02-01 | 1995-04-25 | Chemie Linz Gmbh | COPOLYMERS BASED ON MALEINIC ACID DERIVATIVES AND VINYL MONOMERS, THEIR PRODUCTION AND USE |
US5443636B1 (en) * | 1994-07-29 | 1999-07-13 | Fritz Ind Inc | Composition for and method of pumping concrete |
MY114306A (en) * | 1995-07-13 | 2002-09-30 | Mbt Holding Ag | Cement dispersant method for production thereof and cement composition using dispersant |
FR2742432B1 (en) * | 1995-12-15 | 1998-02-06 | Spie Fondations | RIGIDIFICATION ACCELERATOR, GROUT FOR SEALING AND / OR CONSOLIDATION OF SOILS AND CONSTRUCTION MATERIALS RELATING TO SUCH AN ACCELERATOR, METHODS USING SUCH GROUT |
US6384111B1 (en) | 1996-12-20 | 2002-05-07 | Basf Aktiengesellschaft | Polymers containing carboxyl groups and polyalkylene ether side- chains as additives in mineral building materials |
DE19723474A1 (en) * | 1997-06-04 | 1998-12-17 | Clariant Gmbh | Process for processing a plastic-modified shotcrete or shot mortar |
US5854386A (en) * | 1997-08-25 | 1998-12-29 | Arco Chemical Technology, L.P. | Stabilizers for polymer polyols |
DE19854476C2 (en) * | 1998-11-25 | 2002-04-11 | Dyckerhoff Ag | Hydraulic binder composition free of sulfate carrier and its use |
DE19854477C2 (en) * | 1998-11-25 | 2002-03-14 | Dyckerhoff Ag | Fastest-setting hydraulic binder composition and its use |
DE19914975A1 (en) | 1999-04-01 | 2000-10-05 | Espe Dental Ag | Polyelectrolyte cement used as dental material has organic coating on all of part of metal-releasing component and/or water-soluble polyelectrolyte |
US6528593B1 (en) | 1999-09-10 | 2003-03-04 | The Dow Chemical Company | Preparing copolymers of carboxylic acid, aromatic vinyl compound and hydrophobic polyalkylene oxide |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1111711A (en) * | 1964-08-05 | 1968-05-01 | Fisons Ind Chemicals Ltd | Plaster compositions |
US4046584A (en) * | 1976-04-29 | 1977-09-06 | Snyder Raymond C | Liquid concrete accelerating mixtures and methods for use thereof |
US4650523A (en) * | 1984-06-08 | 1987-03-17 | Onoda Cement Co., Ltd. | Cement accelerating agent |
JPS63162563A (en) * | 1986-12-25 | 1988-07-06 | 大日本インキ化学工業株式会社 | Cement dispersant |
JPH01226757A (en) * | 1988-03-04 | 1989-09-11 | Takemoto Oil & Fat Co Ltd | Dispersing agent for cement |
DE3825161A1 (en) * | 1988-07-23 | 1990-01-25 | Henkel Kgaa | DUST BINDERS FOR THE CONCRETE SPRAYING PROCESS (II) |
-
1988
- 1988-08-09 JP JP63197192A patent/JPH0248453A/en active Granted
-
1989
- 1989-07-31 DE DE3925306A patent/DE3925306A1/en not_active Withdrawn
- 1989-08-04 CH CH2898/89A patent/CH678620A5/de not_active IP Right Cessation
- 1989-08-07 AU AU39401/89A patent/AU622467B2/en not_active Ceased
- 1989-08-07 GB GB8918019A patent/GB2221673B/en not_active Expired - Lifetime
- 1989-08-08 FR FR8910686A patent/FR2635320B1/en not_active Expired - Fee Related
- 1989-08-08 IT IT8921478A patent/IT1231777B/en active
- 1989-08-08 BR BR898903983A patent/BR8903983A/en not_active Application Discontinuation
- 1989-08-08 AT AT0189889A patent/ATA189889A/en not_active Application Discontinuation
- 1989-08-08 ES ES8902820A patent/ES2018382A6/en not_active Expired - Lifetime
- 1989-08-09 BE BE8900855A patent/BE1003765A5/en not_active IP Right Cessation
- 1989-08-09 CA CA000607887A patent/CA1337871C/en not_active Expired - Fee Related
-
1994
- 1994-12-01 HK HK134194A patent/HK134194A/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
JPH0553743B2 (en) | 1993-08-10 |
FR2635320B1 (en) | 1993-09-24 |
BR8903983A (en) | 1990-03-20 |
GB2221673B (en) | 1992-11-11 |
CH678620A5 (en) | 1991-10-15 |
IT1231777B (en) | 1991-12-21 |
AU3940189A (en) | 1990-02-15 |
CA1337871C (en) | 1996-01-02 |
HK134194A (en) | 1994-12-09 |
GB2221673A (en) | 1990-02-14 |
ES2018382A6 (en) | 1991-04-01 |
ATA189889A (en) | 1994-06-15 |
BE1003765A5 (en) | 1992-06-09 |
AU622467B2 (en) | 1992-04-09 |
IT8921478A0 (en) | 1989-08-08 |
GB8918019D0 (en) | 1989-09-20 |
DE3925306A1 (en) | 1990-02-15 |
FR2635320A1 (en) | 1990-02-16 |
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