JPH0473312A - Filling method of clearance for civil engineering and construction work and composition for filler thereof - Google Patents
Filling method of clearance for civil engineering and construction work and composition for filler thereofInfo
- Publication number
- JPH0473312A JPH0473312A JP18541790A JP18541790A JPH0473312A JP H0473312 A JPH0473312 A JP H0473312A JP 18541790 A JP18541790 A JP 18541790A JP 18541790 A JP18541790 A JP 18541790A JP H0473312 A JPH0473312 A JP H0473312A
- Authority
- JP
- Japan
- Prior art keywords
- foaming
- filler
- zeolite
- amount
- construction
- 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
- 239000000945 filler Substances 0.000 title claims abstract description 25
- 238000010276 construction Methods 0.000 title claims description 23
- 239000000203 mixture Substances 0.000 title claims description 19
- 238000000034 method Methods 0.000 title claims description 14
- 239000010457 zeolite Substances 0.000 claims abstract description 29
- 239000000463 material Substances 0.000 claims abstract description 28
- 229910021536 Zeolite Inorganic materials 0.000 claims abstract description 26
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims abstract description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000000843 powder Substances 0.000 claims abstract description 13
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 10
- 239000004088 foaming agent Substances 0.000 claims description 20
- 239000004568 cement Substances 0.000 claims description 15
- 239000008187 granular material Substances 0.000 claims description 7
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims description 7
- 235000012239 silicon dioxide Nutrition 0.000 claims description 7
- 238000002156 mixing Methods 0.000 claims description 4
- 239000000654 additive Substances 0.000 claims description 3
- 230000000996 additive effect Effects 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims description 2
- 235000011941 Tilia x europaea Nutrition 0.000 claims description 2
- 239000011575 calcium Substances 0.000 claims description 2
- 229910052791 calcium Inorganic materials 0.000 claims description 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims description 2
- 239000000920 calcium hydroxide Substances 0.000 claims description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims description 2
- 235000011116 calcium hydroxide Nutrition 0.000 claims description 2
- 239000002734 clay mineral Substances 0.000 claims description 2
- 239000004571 lime Substances 0.000 claims description 2
- 235000019353 potassium silicate Nutrition 0.000 claims description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 2
- 239000002562 thickening agent Substances 0.000 claims description 2
- 239000010440 gypsum Substances 0.000 claims 1
- 229910052602 gypsum Inorganic materials 0.000 claims 1
- 229910001387 inorganic aluminate Inorganic materials 0.000 claims 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical group [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 abstract description 5
- 238000007596 consolidation process Methods 0.000 abstract description 4
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical group [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 abstract description 2
- 229910052909 inorganic silicate Inorganic materials 0.000 abstract 4
- 230000002349 favourable effect Effects 0.000 abstract 1
- 238000005187 foaming Methods 0.000 description 41
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 238000001816 cooling Methods 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000007789 gas Substances 0.000 description 6
- 238000002347 injection Methods 0.000 description 6
- 239000007924 injection Substances 0.000 description 6
- 239000013307 optical fiber Substances 0.000 description 6
- 230000029058 respiratory gaseous exchange Effects 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 4
- 239000002657 fibrous material Substances 0.000 description 4
- 238000004898 kneading Methods 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 230000003014 reinforcing effect Effects 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- -1 alkyl sulfones Chemical class 0.000 description 3
- 239000004567 concrete Substances 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 238000004880 explosion Methods 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 239000004113 Sepiolite Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 150000004645 aluminates Chemical class 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- AIIBUKTUNWMKGX-UHFFFAOYSA-N calcium hydrogen peroxide dihypochlorite Chemical compound OO.Cl[O-].[Ca+2].Cl[O-] AIIBUKTUNWMKGX-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000011038 discontinuous diafiltration by volume reduction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 238000005429 filling process Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000011440 grout Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000012774 insulation material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- NCYVXEGFNDZQCU-UHFFFAOYSA-N nikethamide Chemical compound CCN(CC)C(=O)C1=CC=CN=C1 NCYVXEGFNDZQCU-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920002120 photoresistant polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000011513 prestressed concrete Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- YZYDOFGGDSDUPX-UHFFFAOYSA-M sodium;carbonic acid;chloride Chemical compound [Na+].[Cl-].OC(O)=O YZYDOFGGDSDUPX-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Consolidation Of Soil By Introduction Of Solidifying Substances Into Soil (AREA)
- Soil Conditioners And Soil-Stabilizing Materials (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、土木建築工事用間隙充てん方法及びその充て
ん材用組成物に関するものである。さらに詳しくいえば
、本発明は、トンネル覆工部の裏込めや覆工の補強、地
下構造物背面の間隙や地盤沈下によって生じた空洞への
充てん、地盤内の間隙充てん、地下埋設物工事に伴う埋
め戻し等に好適に用いられる土木建築工事用間隙充てん
方法及びその充てん材用組成物に関するものである。こ
の方法は、簡単かつ容易に、過不足なく、しかも安全に
間隙を充てんするものである。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a method for filling gaps in civil engineering and construction work and a composition for the filler. More specifically, the present invention is suitable for backfilling tunnel linings, reinforcing linings, filling gaps at the back of underground structures and cavities caused by ground subsidence, filling gaps in the ground, and for underground construction work. The present invention relates to a method for filling gaps in civil engineering and construction work, which is suitably used for backfilling and the like, and a composition for the filler. This method fills the gap simply and easily, without too much or too little, and safely.
従来の技術
土木建築工事において、裏込め注入材や間隙光てん材な
どとしては、セメントを主体に砂利、砂、粘土等を混合
したもの、さらにこれに物理的に気泡を導入させるため
の起泡剤、又は化学反応によりガスを発生させるための
発泡剤を添加したもの、急結性を付与したものなど種々
のものが用いられている。中でも、起泡剤や発泡剤を添
加したものは、流動性、ポンプ圧送性、材料分離性、経
済性等に優れているため施工実績が多い。Conventional technology In civil engineering and construction work, backfill injection materials and gap fill materials are mainly made of cement mixed with gravel, sand, clay, etc., and foaming is used to physically introduce air bubbles into this material. A variety of materials are used, including those to which foaming agents or foaming agents are added to generate gas through chemical reactions, and those to which quick-setting properties are added. Among these, those with foaming agents or blowing agents added have many construction results because they have excellent fluidity, pumpability, material separation, economic efficiency, etc.
この起泡剤は界面活性作用により材料混練中に物理的に
気泡を導入させるもので、ロジン石けん、アニオン系界
面活性剤、ノニオン系界面活性剤、ゼラチンやカゼイン
等のタンパク買の誘導体、アルキルスルホン酸塩などを
主成分とするものである。しかしながら、これらの起泡
剤は添加量、及びミキサーの大きさ、羽根の形状、羽根
の回転数、かくはん時間などの混線条件により発泡状況
が異なるため、現場において気泡量、流動性、強度など
の品質を常に一定に保つことが困難であるし、また材料
混練中に物理的に気泡を導入させるため均一な気泡が得
られに〈<、気泡の大きさノこバラツキを生じて充てん
材の上層部には大きな気泡が集まりやすくなるが、その
ため体積減少を起こして空洞を形成しやすく密充てんが
困難になるという欠点がある。This foaming agent physically introduces air bubbles during material kneading through its surfactant action, and is used in rosin soaps, anionic surfactants, nonionic surfactants, proteinaceous derivatives such as gelatin and casein, and alkyl sulfones. The main components are acid salts. However, the foaming conditions of these foaming agents vary depending on the amount added and cross-talk conditions such as the size of the mixer, the shape of the blades, the number of rotations of the blades, and the stirring time. It is difficult to keep the quality constant, and because air bubbles are physically introduced during material kneading, it is difficult to obtain uniform air bubbles. Large air bubbles tend to gather in the area, but this has the disadvantage that it tends to reduce volume and form cavities, making it difficult to fill them tightly.
一方、前記発泡剤としては、代表的にはアルミニウム粉
末が挙げられる他、過酸化水素−次亜塩素酸カルシウム
、塩酸−重炭酸ナトリウムなどの二成分系なども用いら
れる。しかしながら、アルミニウム粉末は、−照的にプ
レパツクドコンクリート用モルタル、プレストレストコ
ンクリート用グラウト、気泡コンクリート等に用いられ
、その使用量はセメント重量に対して0.O1%程度に
すぎないが、間隙光てん剤としてアルミニウム粉末を用
いる場合は、上記用途に用いる量の数倍〜数十倍が必要
となるし、またアルミニウム粉末の添加量が多くなると
発泡はある時間より急激に起こり始めて発泡量のコント
ロールが極めて困難になり、発泡に伴う発熱により充て
ん材そのものの硬化時間が短縮され、急激な発泡圧の上
昇によりトンネル躯体のような工事躯体に不測の損壊を
及ぼし、均一な発泡固結体が得られないし、また前記発
泡剤は水素ガスを発生させるものであって、例えば金属
アルミニウム粉末はアルカリとの反応により水素ガスを
発生させるものであるため、爆発限界の低い水素ガスの
爆発の危険性があるなど安全上取り扱いに<<、また金
属アルカリは火災のおそれのある危険物であり、作業性
に難があるという欠点を有する。On the other hand, as the foaming agent, aluminum powder is typically used, as well as two-component systems such as hydrogen peroxide-calcium hypochlorite, hydrochloric acid-sodium bicarbonate, and the like. However, aluminum powder is generally used in mortar for prepacked concrete, grout for prestressed concrete, aerated concrete, etc., and the amount used is 0.00% relative to the weight of cement. Although it is only about 1% of O, when using aluminum powder as a gap photonic agent, the amount required is several to several tens of times the amount used for the above purpose, and if the amount of aluminum powder added is large, foaming may occur. It begins to occur rapidly over time, making it extremely difficult to control the amount of foaming, and the curing time of the filler itself is shortened due to the heat generated by foaming, and the sudden increase in foaming pressure can cause unexpected damage to construction structures such as tunnel frameworks. In addition, the foaming agent generates hydrogen gas, and metal aluminum powder, for example, generates hydrogen gas by reacting with alkali, so it has an explosive limit. However, metal alkalis have the drawbacks of being difficult to handle safely, such as the risk of explosion due to low hydrogen gas, and metal alkalis are dangerous materials that may cause a fire, making them difficult to work with.
発明が解決しようとする課題
本発明は、このような従来の発泡性充てん材を用いた充
てん方法のもつ欠点を克服し、施工時のブリージング量
が少なく、作業性が良好であり、固結後の均一性に優れ
た間隙光てん材を見出し、かつ眩光てん材においては発
泡が比較的緩徐に進行し、発泡圧も適度であることを利
用することによって、トンネル覆工部の裏込めや覆工の
補強、地下構造物背面のM隙への充てん、地盤内の間隙
光てん、地下埋設物工事に伴う埋め戻し等を効果的に施
工する方法を提供することを目的としてなされたもので
ある。Problems to be Solved by the Invention The present invention overcomes the drawbacks of the conventional filling method using foamable fillers, has a small amount of breathing during construction, has good workability, and has a By discovering a light-gap roofing material with excellent uniformity, and by taking advantage of the fact that foaming progresses relatively slowly and the foaming pressure is moderate in the glare-shielding material, it is possible to backfill and cover tunnel linings. The purpose of this work is to provide an effective method for reinforcing concrete structures, filling the M gap at the back of underground structures, filling gaps in the ground, backfilling for underground construction, etc. .
課題を解決するための手段
本発明者らは、前記の好ましい特徴を有する土木建築工
事用間隙充てん方法を開発するために種々研究を重ねた
結果、発泡性無機ケイ酸系粉・粒体、中でもゼオライト
、特に焼成ゼオライトが水を加えられると多量の気泡を
発生して発泡剤として機能することに着目し、これを凝
結硬化材に作用させることにより、その目的を達成しう
ろことを見出し、この知見tこ基づいて本発明を完成す
るに至っt;。Means for Solving the Problems The present inventors have conducted various studies to develop a gap filling method for civil engineering and construction work having the above-mentioned preferable characteristics. Focusing on the fact that zeolite, especially calcined zeolite, generates a large amount of bubbles when water is added and functions as a foaming agent, he discovered that this purpose could be achieved by applying this to a hardening material. Based on this knowledge, we have completed the present invention.
すなわち、本発明は、凝結硬化材に発泡性無機ケイ酸系
粉・粒体と水とを加えることによって調製された充てん
材を土木建築工事における間隙に充てんすることを特徴
とする施工方法を提供するものである。That is, the present invention provides a construction method characterized by filling gaps in civil engineering and construction work with a filler prepared by adding foamable inorganic silicic acid powder/granules and water to a hardened material. It is something to do.
以下、本発明の詳細な説明する。The present invention will be explained in detail below.
本発明において用いる発泡性無機ケイ酸系粉・粒体とし
ては、ケイ酸アルミニウム系のものが好ましく、中でも
ゼオライト、特に焼成ゼオライトが好ましい。ゼオライ
トは、天然ゼオライト、合成ゼオライトのいずれでも差
し支えないが、天然ゼオライトが一般的である。また、
焼成ゼオライトは、通常これらのゼオライトを粉砕分級
して所定粒度に調整したのち、100〜700℃、好ま
しくは400〜600℃に焼成することによって得られ
、通常焼成後に自然放冷、室温への徐冷、より低温への
強制冷却等を施したものが好ましく用いられる。The foamable inorganic silicic acid powder/granules used in the present invention are preferably aluminum silicate powders, and zeolites, particularly calcined zeolites, are particularly preferred. The zeolite may be either a natural zeolite or a synthetic zeolite, but natural zeolite is common. Also,
Calcined zeolite is usually obtained by crushing and classifying these zeolites to adjust the particle size to a predetermined size, and then calcining it at 100 to 700℃, preferably 400 to 600℃. Those subjected to cooling or forced cooling to a lower temperature are preferably used.
特に、この焼成ゼオライトは10℃以下の低温で乾燥空
気を吸着させながら、低温に強制冷却して利用すると、
発泡量が増大するので好ましい。例えば、第1図は50
0℃に焼成したゼオライトの強制冷却温度と発泡量との
関係を示すグラフであるが、これから、強制冷却温度が
低い程、発泡量が増大することが分る。このように、焼
成ゼオライトは強制冷却温度を変えることによって発泡
量の調整が可能である。前記強制冷却は、常法、例えば
冷凍倉庫中に所定条件例えば所定温度で所定時間保持す
るなどの方法により行われる。In particular, when this calcined zeolite is used by forcing it to cool to a low temperature while adsorbing dry air at a low temperature of 10 degrees Celsius or less,
This is preferred because the amount of foaming increases. For example, Figure 1 shows 50
This is a graph showing the relationship between the forced cooling temperature of zeolite calcined to 0° C. and the amount of foaming, and it can be seen from this graph that the lower the forced cooling temperature is, the more the amount of foaming increases. In this way, the amount of foaming of calcined zeolite can be adjusted by changing the forced cooling temperature. The forced cooling is carried out by a conventional method, for example, by holding the product in a frozen warehouse under predetermined conditions, such as at a predetermined temperature, for a predetermined period of time.
前記無機ケイ酸系粉・粒体は、例えばゼオライトがケイ
酸塩の5iOzの四面体が重合した結晶構造を有してい
るように、一般に特有の結晶構造を有し、結晶内の空間
には通常窒素等の発泡性気体や水などが取りこまれ、特
にその中の水は適切な温度で焼成することにより空気中
の窒素等により置換されるものと推測される。発泡機構
はこの窒素等の発泡性気体と水との置換が行われ、窒素
ガスが発生する作用によるものであり、このガスの微小
気泡が材料中に均等に発生し均一な発泡固結体が生成さ
れるものと推測される。窒素ガスは安定なガスであり、
不燃性のため爆発の心配がない。The inorganic silicic acid powder/granules generally have a unique crystal structure, for example, like zeolite, which has a crystal structure in which 5iOz tetrahedrons of silicate are polymerized, and the spaces within the crystals are Usually, a foaming gas such as nitrogen, water, etc. are introduced, and it is assumed that the water contained therein is replaced by nitrogen, etc. in the air by firing at an appropriate temperature. The foaming mechanism is due to the action of replacing foaming gas such as nitrogen with water and generating nitrogen gas, and microbubbles of this gas are evenly generated in the material to form a uniform foamed solid. It is assumed that this will be generated. Nitrogen gas is a stable gas;
There is no risk of explosion as it is non-flammable.
本発明において用いる凝結硬化材としては、例えばセメ
ント、セラコラ、石灰、消石灰、あるいはこれらの混合
物、あるいはこれらに砂などの細雪材、砂利、れきなど
の粗骨材等の少なくとも1種の骨材、あるいは粘土、フ
ライアッシュ、スラグ、ソラスなどの少なくとも1種の
増量材、あるいはこれら骨材と増量材の両方を配合して
成る組成物などを挙げることができる。The hardening material used in the present invention includes, for example, cement, Ceracola, lime, slaked lime, or a mixture thereof, or at least one kind of aggregate such as fine snow material such as sand, coarse aggregate such as gravel, gravel, etc. Alternatively, at least one type of filler such as clay, fly ash, slag, and solas, or a composition containing both of these aggregates and fillers may be used.
本発明において、発泡性無機ケイ酸系粉・粒体の使用量
は凝結硬化材の種類や使用目的等に応じて種々変動する
が、両者の合計量に対し、通常5〜70重量%、好まし
くは10〜40重量%の範囲で選ばれる。この量が5重
量%未満では発泡量が少なく本発明の効果が十分に発揮
されないし、また70重量%を超えると強度が低下する
のを免れない。In the present invention, the amount of the expandable inorganic silicic acid powder/granules used varies depending on the type of hardening agent and the purpose of use, but is usually 5 to 70% by weight, preferably 5% to 70% by weight based on the total amount of both. is selected in the range of 10 to 40% by weight. If this amount is less than 5% by weight, the amount of foaming will be small and the effects of the present invention will not be fully exhibited, and if it exceeds 70% by weight, the strength will inevitably decrease.
また、本発明においては、混和剤として起泡剤又は発泡
剤、急硬化性添加剤及び粘性付与剤の中から選ばれた少
なくとも1種を配合することもできる。Further, in the present invention, at least one selected from a foaming agent, a foaming agent, a rapidly curing additive, and a viscosity imparting agent can also be blended as an admixture.
この起泡剤は物理的に気泡を導入しうるものであればい
かなるものでもよく、例えばアニオン系界面活性剤やノ
ニオン系界面活性剤又はアルキルスルホン酸塩を成分と
するものなどを挙げることができる。This foaming agent may be any agent as long as it can physically introduce bubbles, and examples include those containing anionic surfactants, nonionic surfactants, or alkyl sulfonates. .
また、発泡剤は化学反応によりガスを発生しうるもので
あればよく、例えばアルミニウム粉末、マグネシウム粉
末などが用いられる。Further, the foaming agent may be any foaming agent as long as it can generate gas through a chemical reaction, and for example, aluminum powder, magnesium powder, etc. are used.
また、急硬化性添加剤は急硬性を付与しうるものであれ
ば特に制限されず、例えば水ガラス、アルミン酸塩、炭
酸ナトリウムのような炭酸塩などの急結性無機塩、セメ
ント鉱物、カルシウムスルホアルミネートなどの少なく
とも1種の急結剤を主成分とするものが用いられる。In addition, the rapid hardening additive is not particularly limited as long as it can impart rapid hardening, and examples include water glass, aluminate, rapid hardening inorganic salts such as carbonates such as sodium carbonate, cement minerals, and calcium. A material containing at least one quick setting agent such as sulfoaluminate as a main component is used.
また、粘性付与剤は粘性を付与しうるものであれば特に
制限されず、例えばベントナイト、セピオライトなどの
粘土鉱物や、カルボキシメチルセルロース、セルロース
エーテル系化合物、アクリル系高分子化合物などの有機
系増粘剤などが用いられる。Further, the viscosity imparting agent is not particularly limited as long as it can impart viscosity, and examples include clay minerals such as bentonite and sepiolite, and organic thickeners such as carboxymethyl cellulose, cellulose ether compounds, and acrylic polymer compounds. etc. are used.
以上の各種成分からなる組成物は、施工に際し、水を加
えることによって所望の間隙光てん材を調製することが
できる。この際十分に混練するのが好ましい。水の配合
量は通常間隙光てん材令量に対して10〜100重量%
、好ましくは15〜70重量%の範囲で選ばれる。この
配合量が10重量%未満ではスラリー化が不十分で本発
明の効果が十分に発揮されないし、また100重量%を
超えると、強度が低下するのを免れない。A composition consisting of the various components described above can be used to prepare a desired gap light beam material by adding water at the time of construction. At this time, it is preferable to thoroughly knead. The amount of water added is usually 10 to 100% by weight based on the amount of light insulation material.
, preferably in the range of 15 to 70% by weight. If this amount is less than 10% by weight, slurry formation will be insufficient and the effects of the present invention will not be fully exhibited, and if it exceeds 100% by weight, the strength will inevitably decrease.
このようにして得られた間隙光てん材の発泡は通常1〜
5時間程度継続するが、混練後5〜20分程度で最終発
泡量の50〜80%程度の発泡量となるため、残りの5
0〜20%程度の発泡余力により充てん材の充てん施工
後も充てん不足や小空隙に対して充てん材が膨張して侵
入することとなり、良好な充てん性が得られる。The foaming rate of the gap-filled optical fiber material obtained in this way is usually 1 to 1.
It continues for about 5 hours, but the foaming amount reaches about 50 to 80% of the final foaming amount in about 5 to 20 minutes after kneading, so the remaining 5 hours
Due to the remaining foaming force of about 0 to 20%, the filler expands and invades insufficient filling or small voids even after filling with the filler, resulting in good filling performance.
例えば、トンネル覆工背面への空洞光てんにおいては、
一般に覆工に対する影響を考慮し、注入圧を2〜3kg
f/crx”と比較的小さな値を目安として充てんを管
理するが、覆工にクラックが発生していたり、巻厚不足
が存在する場合においては、さらに小さな注入圧に制約
される。しかし、そのような小さな注入圧では十分な充
てんが行われにくく、充てん後も来光てん部分を残すお
それが多い。そのため、このような充てん不足部分を補
うために事後光てん性が要望されている。For example, in the case of hollow light beams on the back of tunnel lining,
In general, the injection pressure is set at 2 to 3 kg, taking into account the effect on the lining.
Filling is controlled using a relatively small value of "f/crx" as a guideline, but if cracks occur in the lining or there is insufficient winding thickness, the injection pressure is restricted to an even smaller value. With such a small injection pressure, it is difficult to perform sufficient filling, and there is a high risk that a photoresist area will remain even after filling.Therefore, post-response photoresistance is required to compensate for such an insufficiently filled area.
本発明方法によれば、充てん材は数十分にわたり緩徐に
発泡するため、注入後もなお発泡し続けることから、覆
工に対する影響の全くない小さな注入圧以下で注入を終
えても、その後の充てん材の発泡によって良好な充てん
を期待することができる。しかも、充てん材の発泡圧は
微小で(lJ+s+f/c112以下)、数kgf/c
lI2以上の発泡圧を生じるアルミニウム粉末などを用
いた充てん材とは異なり、覆工への影響を心配すること
はない。また、発泡によって生じた泡は微細で均一性に
富むことから、従来の起泡剤を用いたもののように表層
部の泡が抜け、体積減少を起こすおそれも極めて少ない
。According to the method of the present invention, since the filler foams slowly over several tens of minutes, it continues to foam even after injection. Good filling can be expected by foaming the filler. Moreover, the foaming pressure of the filler is very small (lJ+s+f/c112 or less), several kgf/c.
Unlike fillers using aluminum powder, etc., which generate foaming pressures of 1I2 or higher, there is no need to worry about the effect on the lining. In addition, since the bubbles generated by foaming are fine and highly uniform, there is very little risk of the bubbles falling out of the surface layer and causing a volume reduction, unlike when using conventional foaming agents.
したがって、本発明方法はトンネル覆工部の裏込めや覆
工の補強、地下構造物背面の間隙光てん等の目的に極め
て適合するものである。Therefore, the method of the present invention is extremely suitable for purposes such as backfilling tunnel linings, reinforcing linings, and lighting gaps on the back of underground structures.
この間隙光てん材の特性を添付図面により説明すると、
第2図は、セメントとゼオライトの合計量に対する水の
割合が60重量%である間隙光てん材についてセメント
に対するゼオライトの配合量比と発泡量との関係を示す
グラフである。The characteristics of this gap light reinforcement material are explained using the attached drawings.
FIG. 2 is a graph showing the relationship between the blending ratio of zeolite to cement and the amount of foaming for an interstitial fiber material in which the ratio of water to the total amount of cement and zeolite is 60% by weight.
これより、ゼオライトの配合を多くすることにより、あ
るところまで例えば第2図の場合には前記配合量比が0
.1までは発泡量もほぼ比例的に増大するが、それを超
えるとゼオライトの配合を多くしても発泡量はあまり増
大しなくなることが分る。From this, by increasing the amount of zeolite blended, for example, in the case of Figure 2, the blending ratio becomes 0.
.. It can be seen that up to 1, the amount of foaming increases almost proportionally, but beyond that, even if the amount of zeolite is increased, the amount of foaming does not increase much.
また、菓3rl!Jに、種々の発泡性物質を含む下記A
−1、A−2、X及びYの間隙光てん材用組成物を、そ
れに対し重量比で60%量の水と共に混練して充てん材
を調製してからの経過時間と発泡量との関係をグラフで
示す。A−1及びA−2は本発明のものであって、セメ
ントと、 500’Cに焼t、t&20℃に冷却した#
!成ゼオライトとの重量比が前者では2:1、後者では
5:lのものであり、X及びYは比較のためのもので、
Xはセメントに対して起泡剤(サンコーコロイド社製、
商品名サンコーGP)0.3重量%を配合して成る組成
物、Yはセメントに対してアルミニウム0.03重量%
を配合して成る組成物である。Also, Ka3rl! J, the following A containing various foaming substances
- Relationship between the elapsed time and foaming amount after preparing the filler by kneading the gap optical fiber compositions of -1, A-2, X, and Y with water in an amount of 60% by weight. is shown in a graph. A-1 and A-2 are those of the present invention, consisting of cement and #1 calcined to 500'C, t & cooled to 20°C.
! The weight ratio with synthetic zeolite is 2:1 for the former and 5:1 for the latter, and X and Y are for comparison.
X is a foaming agent for cement (manufactured by Sanko Colloid Co., Ltd.,
A composition comprising 0.3% by weight of aluminum (trade name Sanko GP), Y is 0.03% by weight of aluminum based on cement.
This is a composition comprising:
このグラフより、従来の起泡剤を用いた場合には時間の
経過による発泡量の変化はほとんどなく、また従来の発
泡剤を用いた場合では3分経過後より急激に発泡量が増
大するのに対し、本発明のゼオライトを用いた間隙光て
ん材用組成物では、10分経過後で最終発泡量の60〜
70%程度発泡し、残40〜30%の発泡量分について
は緩やかに発泡が進行して、充てん施工作業後も充てん
不足部分や小空隙に対して充てん材が侵入し、優れた充
てん効果が得られることが分る。This graph shows that when using a conventional foaming agent, there is almost no change in the amount of foaming over time, and when using a conventional foaming agent, the amount of foaming increases rapidly after 3 minutes. On the other hand, in the composition for interstitial optical fiber materials using the zeolite of the present invention, the final foaming amount was 60 to 60% after 10 minutes.
Approximately 70% foaming occurs, and the remaining 40-30% foaming progresses slowly, allowing the filler to penetrate into areas with insufficient filling and small voids even after the filling process, resulting in an excellent filling effect. I know what I can get.
次に、セメント5重量部とゼオライト1重量部から成る
本発明の組成物に対し水60!i量%を配合して成るゼ
オライト系間隙光てん材について、ミキサーを用いて1
40rpmで混練し、注形型中に入れ、1日間放置して
固結させた。この過程で生じたブリージング量及び発泡
量を測定した。また、固結生成物全体を上中下三層に等
分に切断してそれぞれの平均単位体積重量を求めた。そ
の結果を表に示す。Next, a composition of the present invention consisting of 5 parts by weight of cement and 1 part by weight of zeolite is compared with 60 parts by weight of water. Regarding the zeolite-based interstitial fiber material containing i amount%,
The mixture was kneaded at 40 rpm, placed in a casting mold, and left to solidify for one day. The amount of breathing and foaming that occurred during this process was measured. In addition, the entire solidified product was equally cut into three layers, upper, middle, and lower, and the average unit volume weight of each layer was determined. The results are shown in the table.
また、比較のためにセメントに対し、水6o重量%及び
アルミニウム粉末0−03重量%を配合して成る間隙光
てん材用組成物(以下、比較試料1という)、及びセメ
ントに対し、水60重量%及び起泡剤(サンコーコロイ
ド社製、商品名サンコラGP)0.03重量%を配合し
て成る間隙光てん材用組成物(以下、比較試料2という
)について、上記光てん材と同様にして固結後のブリー
ジング量、発泡量及び上中下三層の平均単位体積重量を
求めt;。その結果も表に示す。For comparison, we also prepared a composition for a gap optical fiber material (hereinafter referred to as Comparative Sample 1), which was prepared by adding 60% by weight of water and 0-03% by weight of aluminum powder to cement, and 60% by weight of water to cement. Regarding a composition for a gap optical fiber material (hereinafter referred to as comparative sample 2), which contains 0.03 weight percent of a foaming agent (manufactured by Sanco Colloid Co., Ltd., trade name Sancora GP), the same composition as the above optical fiber material was used. The amount of breathing after solidification, the amount of foaming, and the average unit volume weight of the upper, middle, and lower three layers were determined. The results are also shown in the table.
これより、比較試料l及び2はいずれもブリージング量
が多く、その上に比較試料2の場合にはより下の層程平
均単位体積重量が高く、固結後の充てん材全体にわたっ
ての均一性が低下するのを免れないのに対し、本発明の
組成物から得られた間隙光てん材はブリージング量が少
なく、シかも固結後の均一性に優れることが分る。From this, both Comparative Samples 1 and 2 have a large amount of breathing, and in addition, in the case of Comparative Sample 2, the lower the layer, the higher the average unit volume weight, and the uniformity over the entire filler after consolidation. On the other hand, it can be seen that the gap fiber material obtained from the composition of the present invention has a small amount of breathing and excellent uniformity after solidification.
発明の作用、効果
本発明方法によれば、施工時のブリージング量が少なく
、作業性が良好であり、固結後の均一性に優れ、かつ発
泡が比較的緩徐に進行し、発泡圧も適度であるという顕
著な効果を奏する。Functions and Effects of the Invention According to the method of the present invention, the amount of breathing during construction is small, the workability is good, the uniformity after consolidation is excellent, the foaming progresses relatively slowly, and the foaming pressure is also moderate. It has the remarkable effect of
したがって、本発明方法は、土木工事、特にトンネル覆
工部の裏込めや覆工の補強、地下構造物背面の間隙や地
盤沈下によって生じた空洞への充てん、軟弱地盤改良工
事、特に軟弱地盤用圧密注入工事等における地盤内の間
隙光てん、地下埋設物工事に伴う埋め戻し等に好適に利
用しうる。Therefore, the method of the present invention is useful for civil engineering works, especially for backfilling tunnel linings and reinforcing linings, filling gaps at the back of underground structures and cavities caused by ground subsidence, and soft ground improvement work, especially for soft ground. It can be suitably used for light holes in the ground during consolidation injection work, backfilling for underground construction work, etc.
また、本発明組成物はそれに単に水を加えるだけで前記
本発明方法に用いる充てん材を簡単に調製することがで
きる。Moreover, the filler used in the method of the present invention can be easily prepared by simply adding water to the composition of the present invention.
第1図は、焼成ゼオライトの冷却温度と発泡量との関係
を示すグラフ、第2図は、本発明の間隙光てん材用組成
物の1例のセメントに対するゼオライトの配合量比と発
泡量との関係を示すグラフ、第3図は、種々の充てん材
を調製してがらの経過時間と発泡量との関係を示すグラ
フである。
第1図FIG. 1 is a graph showing the relationship between the cooling temperature of calcined zeolite and the amount of foaming, and FIG. 2 is a graph showing the relationship between the ratio of the amount of zeolite to cement and the amount of foaming in an example of the composition for interstitial fiber material of the present invention. FIG. 3 is a graph showing the relationship between elapsed time and foaming amount while preparing various fillers. Figure 1
Claims (1)
加えることによつて調製された充てん材を土木建築工事
における間隙に充てんすることを特徴とする施工方法。 2 凝結硬化材がセメント、石こう、石灰及び消石灰の
中から選ばれた少なくとも1種の無機質硬化性材料に、
少なくとも1種の骨材を配合して成るものである請求項
1記載の施工方法。 3 発泡性無機ケイ酸系粉・粒体が焼成、粉砕したゼオ
ライトである請求項1又は2記載の施工方法。 4 充てん材が起泡剤又は発泡剤を混和剤として配合し
てなるものである請求項1、2又は3記載の施工方法。 5 充てん材が水ガラス、アルミン酸無機物、急結性無
機塩、セメント類及びカルシウムスルホアルミネートの
中から選ばれた少なくとも1種の急結剤を主成分とする
急硬化性添加剤を配合して成るものである請求項1ない
し4のいずれかに記載の施工方法。 6 充てん材が粘土鉱物及び有機系増粘剤の一方又は両
方からなる粘性付与剤を配合して成るものである請求項
1ないし5のいずれかに記載の施工方法。 7 凝結硬化材に発泡性無機ケイ酸系粉・粒体を配合し
て成る土木建築工事用間隙充てん材用組成物。[Scope of Claims] 1. Construction characterized by filling gaps in civil engineering and construction work with a filler prepared by adding foamable inorganic silicic acid powder/granules and water to a hardened material. Method. 2. The setting hardening agent is at least one inorganic hardening material selected from cement, gypsum, lime, and slaked lime,
2. The construction method according to claim 1, further comprising blending at least one type of aggregate. 3. The construction method according to claim 1 or 2, wherein the expandable inorganic silicic acid powder/granules are calcined and crushed zeolite. 4. The construction method according to claim 1, 2 or 3, wherein the filler contains a foaming agent or a foaming agent as an admixture. 5. The filler contains a quick-setting additive containing at least one quick-setting agent selected from water glass, inorganic aluminates, quick-setting inorganic salts, cements, and calcium sulfoaluminate. The construction method according to any one of claims 1 to 4, comprising: 6. The construction method according to any one of claims 1 to 5, wherein the filler contains a viscosity imparting agent consisting of one or both of a clay mineral and an organic thickener. 7. A composition for a gap filler for civil engineering and construction work, which is made by blending a set hardening material with an expandable inorganic silicic acid powder/granule.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2185417A JP2515916B2 (en) | 1990-07-16 | 1990-07-16 | Composition for gap filling material for civil engineering and construction work, gap filling material for civil engineering and construction work, and construction method using the gap filling material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2185417A JP2515916B2 (en) | 1990-07-16 | 1990-07-16 | Composition for gap filling material for civil engineering and construction work, gap filling material for civil engineering and construction work, and construction method using the gap filling material |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP32176695A Division JP2690726B2 (en) | 1995-12-11 | 1995-12-11 | Method for producing highly expandable zeolite |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0473312A true JPH0473312A (en) | 1992-03-09 |
JP2515916B2 JP2515916B2 (en) | 1996-07-10 |
Family
ID=16170425
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JP2185417A Expired - Fee Related JP2515916B2 (en) | 1990-07-16 | 1990-07-16 | Composition for gap filling material for civil engineering and construction work, gap filling material for civil engineering and construction work, and construction method using the gap filling material |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
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JPH08100427A (en) * | 1994-10-03 | 1996-04-16 | Kyokado Eng Co Ltd | Water-permeable lightweight block |
JPH08128044A (en) * | 1994-10-28 | 1996-05-21 | Kyokado Eng Co Ltd | Light-weight earth construction method and light-weight block |
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JPS5535352A (en) * | 1978-09-05 | 1980-03-12 | Tokyo Shibaura Electric Co | Crt display |
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1990
- 1990-07-16 JP JP2185417A patent/JP2515916B2/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
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JPS5535352A (en) * | 1978-09-05 | 1980-03-12 | Tokyo Shibaura Electric Co | Crt display |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08100427A (en) * | 1994-10-03 | 1996-04-16 | Kyokado Eng Co Ltd | Water-permeable lightweight block |
JPH08128044A (en) * | 1994-10-28 | 1996-05-21 | Kyokado Eng Co Ltd | Light-weight earth construction method and light-weight block |
Also Published As
Publication number | Publication date |
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JP2515916B2 (en) | 1996-07-10 |
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