JPH0340185B2 - - Google Patents
Info
- Publication number
- JPH0340185B2 JPH0340185B2 JP20278883A JP20278883A JPH0340185B2 JP H0340185 B2 JPH0340185 B2 JP H0340185B2 JP 20278883 A JP20278883 A JP 20278883A JP 20278883 A JP20278883 A JP 20278883A JP H0340185 B2 JPH0340185 B2 JP H0340185B2
- Authority
- JP
- Japan
- Prior art keywords
- container
- water
- crushing agent
- expandable
- crushing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000003795 chemical substances by application Substances 0.000 claims description 72
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 58
- 238000006703 hydration reaction Methods 0.000 claims description 31
- 239000002002 slurry Substances 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 15
- 230000036571 hydration Effects 0.000 claims description 14
- 239000004567 concrete Substances 0.000 claims description 7
- 230000006378 damage Effects 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 238000010276 construction Methods 0.000 claims description 4
- 230000007423 decrease Effects 0.000 claims description 4
- 239000011435 rock Substances 0.000 claims description 4
- 230000001066 destructive effect Effects 0.000 claims description 3
- 239000002253 acid Substances 0.000 description 19
- 239000000463 material Substances 0.000 description 13
- 239000000243 solution Substances 0.000 description 13
- -1 polyethylene Polymers 0.000 description 12
- 229920003023 plastic Polymers 0.000 description 10
- 239000004033 plastic Substances 0.000 description 10
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 7
- 238000007796 conventional method Methods 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- 239000000292 calcium oxide Substances 0.000 description 6
- 239000004568 cement Substances 0.000 description 6
- 238000002347 injection Methods 0.000 description 6
- 239000007924 injection Substances 0.000 description 6
- 239000004698 Polyethylene Substances 0.000 description 5
- 239000004743 Polypropylene Substances 0.000 description 5
- 239000004793 Polystyrene Substances 0.000 description 5
- 239000003513 alkali Substances 0.000 description 5
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 229920000573 polyethylene Polymers 0.000 description 5
- 229920001155 polypropylene Polymers 0.000 description 5
- 229920002223 polystyrene Polymers 0.000 description 5
- 239000004800 polyvinyl chloride Substances 0.000 description 5
- 229920000915 polyvinyl chloride Polymers 0.000 description 5
- 238000002441 X-ray diffraction Methods 0.000 description 4
- 230000008020 evaporation Effects 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 239000000123 paper Substances 0.000 description 3
- 230000008961 swelling Effects 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000011111 cardboard Substances 0.000 description 2
- 230000029087 digestion Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 239000004570 mortar (masonry) Substances 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 235000012255 calcium oxide Nutrition 0.000 description 1
- 239000012611 container material Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
Landscapes
- Drilling And Exploitation, And Mining Machines And Methods (AREA)
- Working Measures On Existing Buildindgs (AREA)
- Disintegrating Or Milling (AREA)
Description
本発明は破壊工法に係り、特に、膨張性破砕剤
の膨張圧を継続的に発現せしめて被破砕物を効率
的に破砕する破壊工法に関する。
一般に、コンクリート構造物や岩石、地山等の
脆性物体の解体、破砕に酸化カルシウム(CaO)
を主要な成分とする膨張性破砕剤が広く用いられ
ている。
即ち、上記膨張性破砕剤を用いて被破砕物を破
壊する場合には、被破砕物に穿設された穴に膨張
性破砕剤スラリー又は水と膨張性破砕剤を充填
し、膨張性破砕剤と水との反応により発生する水
和膨張圧を利用して被破砕物を破壊するものであ
る。
ところで、膨張性破砕剤の水和反応の進行に伴
つて発生する熱(消化熱)によるスラリー温度の
急激な上昇を原因とするいわゆる噴出現象が起こ
り、膨張性破砕剤スラリーそのものが穴から噴出
してしまう場合がある。このような噴出現象が発
生した場合には、膨張性破砕剤スラリー量が不足
し、膨張圧が減少し破砕力が低下する、という不
具合が存していた。このような噴出現象に対処す
るものとして、水和反応の進行を遅延させる消化
遅延剤を添加する等の方策が採られており、噴出
現象自体を防止することは可能である。しかしな
がら、これらの防止技術をもつてしても水和反応
から生ずる熱による水分の蒸発は防止し得ず、
尚、水和膨張圧が減少してしまう、という欠点が
あつた。
即ち、膨張性破砕剤と水との水和反応により熱
が発生するため膨張性破砕剤スラリー中の水分が
蒸発してしまい、当初設定されていた水/破砕剤
比が崩れてしまうため、膨張圧の発現が緩慢とな
つたり又は膨張性破砕剤の一部が末反応のまま残
存することとなり、充填された膨張性破砕剤を完
全に利用することができないという欠点が存して
いた。
従つて、このような水和反応の進行に伴い発生
する熱による水分の蒸発に対処する方策として、
充填時より、膨張性破砕剤が充分に水和反応を起
こすために必要な理論値以上の高水比の膨張性破
砕剤スラリーを用意し、この膨張性破砕剤により
破砕することも行なわれていた。しかし、このよ
うな高水比の膨張性破砕剤スラリーは低い膨張圧
しか発揮できず予期した破砕効果を上げることが
できない、という欠点があつた。
一方、充填後、水が蒸発した時点で穴内に充填
された膨張性破砕剤スラリーに再注水することも
行なわれていたが、末反応の膨張性破砕剤が急激
に水和反応を起こし、いわゆる噴出現象が生ずる
場合があり、作業者にとつては極めて危険である
と共に、破砕作業に長時間を要してしまうという
欠点が存していた。
本発明はこのような従来の不具合に鑑み為され
たものであつて、その目的とするところは、被破
砕物に穿設された穴内に充填された膨張性破砕剤
スラリーの所定の水和膨張圧を常に維持し、効率
的に被破砕物を破砕できると共に安全且つ円滑に
破砕作業を行なうことが可能な破壊工法を提供す
ることにある。
係る目的達成のため本発明にあつては、水との
反応により発生する水和膨張圧を利用しコンクリ
ート構造物及び岩石等の脆性物体を破壊する破壊
工法において、貯水した容器を被破砕物に開設さ
れた穴内の膨張性破砕剤スラリー中に配置し、水
和膨張圧低下時に該容器を破壊することにより、
該容器内の水を排出させ、水和膨張圧を再度現出
せしめることにより、被破砕物を破砕するように
構成されている。
以下、添付図面に示す実施例と共に本発明を詳
細に説明する。
まず、本発明に使用される容器は、内部に液体
を封入し得る形状及び構造に形成されていること
が必要であり、例えば、直径2cm、長さ20cm程度
に形成された細長袋状のものが用いられる。次
に、本発明に使用される容器の材質は、液体を内
部に封入し得る素材により形成されていることが
必要であり、薄いプラスチツク、紙等が用いられ
る。この内プラスチツクとしては、ポリエチレ
ン、ポリプロピレン、ポリ塩化ビニール、ナイロ
ン、ポリスチレン等の各種の素材が適用され得
る。そして、これらの素材の選定に当つては、使
用されるプラスチツクの軟化点(融点)と膨張性
破砕剤スラリーの最高発熱温度とを勘案して決す
る必要があるが、上記各種のプラスチツクの軟化
点(融点)は表1に示す通りである。
The present invention relates to a destructive construction method, and in particular to a destructive construction method for efficiently crushing objects to be crushed by continuously developing the expansion pressure of an expandable crushing agent. Calcium oxide (CaO) is generally used for demolition and crushing of brittle objects such as concrete structures, rocks, and earth.
Expansive crushing agents containing as the main component are widely used. That is, when destroying an object to be crushed using the above-mentioned expandable crushing agent, a hole made in the object to be crushed is filled with an expandable crushing agent slurry or water and an expandable crushing agent, and the expandable crushing agent is The material to be crushed is destroyed by using the hydration expansion pressure generated by the reaction between the crusher and water. By the way, a so-called blowout phenomenon occurs due to a rapid rise in slurry temperature due to the heat (digestion heat) generated as the hydration reaction of the expandable crushing agent progresses, and the expandable crushing agent slurry itself blows out from the hole. There are cases where this happens. When such an ejection phenomenon occurs, there is a problem that the amount of expandable crushing agent slurry becomes insufficient, the expansion pressure decreases, and the crushing force decreases. To deal with such a gushing phenomenon, measures such as adding a digestion retardant that retards the progress of the hydration reaction have been taken, and it is possible to prevent the gushing phenomenon itself. However, even with these prevention techniques, the evaporation of water due to the heat generated from the hydration reaction cannot be prevented.
However, there was a drawback that the hydration expansion pressure decreased. In other words, heat is generated by the hydration reaction between the expandable crushing agent and water, which causes the moisture in the expandable crushing agent slurry to evaporate, and the initially set water/disrupter ratio collapses, causing the expansion There are disadvantages in that the development of pressure becomes slow or a part of the expandable crushing agent remains unreacted, making it impossible to fully utilize the loaded expandable crushing agent. Therefore, as a measure to deal with the evaporation of water due to the heat generated as the hydration reaction progresses,
From the time of filling, an expandable crushing agent slurry with a water ratio higher than the theoretical value required for the expandable crushing agent to sufficiently cause a hydration reaction is prepared, and crushing is carried out using this expandable crushing agent. Ta. However, such an expandable crushing agent slurry with a high water ratio has the disadvantage that it can only exert a low expansion pressure and cannot achieve the expected crushing effect. On the other hand, water was also re-injected into the expandable crushing agent slurry filled in the hole after the water evaporated after filling, but the final reaction of the expandable crushing agent rapidly caused a hydration reaction, and the so-called A blow-out phenomenon may occur, which is extremely dangerous for workers and has the disadvantage that the crushing operation takes a long time. The present invention has been made in view of such conventional problems, and its purpose is to achieve a predetermined hydration expansion of an expandable crushing agent slurry filled in holes drilled in an object to be crushed. It is an object of the present invention to provide a destruction method that can constantly maintain pressure, efficiently crush objects to be crushed, and perform crushing work safely and smoothly. In order to achieve this objective, the present invention uses a container containing water as an object to be crushed in a destruction method that uses hydration expansion pressure generated by reaction with water to destroy brittle objects such as concrete structures and rocks. By placing in an expandable crushing agent slurry in a drilled hole and destroying the container when the hydration expansion pressure decreases,
It is configured to crush the object by draining the water in the container and making the hydration expansion pressure appear again. Hereinafter, the present invention will be described in detail with reference to embodiments shown in the accompanying drawings. First, the container used in the present invention needs to have a shape and structure that allows liquid to be sealed inside, such as an elongated bag-like container with a diameter of about 2 cm and a length of about 20 cm. is used. Next, the material of the container used in the present invention needs to be made of a material capable of sealing the liquid inside, and thin plastic, paper, etc. are used. Among these, various materials such as polyethylene, polypropylene, polyvinyl chloride, nylon, and polystyrene can be used as the plastic. When selecting these materials, it is necessary to take into account the softening point (melting point) of the plastic used and the maximum exothermic temperature of the expandable crushing agent slurry. (Melting point) is as shown in Table 1.
【表】
また、膨張性破砕剤スラリーの発熱温度は主と
して使用する膨張性破砕剤の種類、被破砕物の物
理的特性(例えば熱伝導率、温度等)及び破砕作
業時の気象、気温、混水量等により定まるもので
あるから、予め予備実験として測定することが望
ましい。
また、本発明の第2の実施態様においては水を
貯蔵した容器は該容器に装着された電熱線に通電
した場合に発生する熱により破壊されるように構
成されている。即ち、第1図に示すように本実施
態様において使用される容器1は、ポリエチレ
ン、ポリプロピレン、ポリ塩化ビニール、ナイロ
ン、ポリスチレン等の薄いプラスチツク材若しく
は厚紙等により作製された長さ20cm、直径2cm程
度の有底の細長袋により形成されており、底面及
び、又は側面の周囲に電熱線ヒータ2を巻装しま
たは容器1を形成する樹脂内に電熱線ヒータ2を
埋設すると共にこの電熱線ヒータ2と電源3に接
続し、該容器1に水を注入し、注入穴を適宜手段
により密封したものである。そして、この容器
は、フツク5を介してワイヤーロープ4により吊
架され、穴内に配設される。本容器は以上のよう
に構成されているので該電熱線ヒータ2に通電す
ることにより発生する熱によつて所望の時間に該
容器1を破壊せしめることが可能となる。尚、上
記容器に使用されるプラスチツクの材質の選定に
当つては、使用プラスチツクの軟化点(融点)と
膨張性破砕剤スラリーの発熱温度とを勘案して決
すべきであり、使用されるプラスチツクの軟化点
(融点)は水和膨張性破砕剤スラリーの発熱温度
よりも高いことが必要となる。何故なら、膨張性
破砕剤スラリーが水和反応を起こす際に発生する
熱により水を貯蔵した容器が破壊されてしまうの
で所望の時間に該電熱線ヒータ2に通電すること
によつて該容器1を破壊せしめることが不可能と
なるからである。このような電熱線ヒータ2が埋
設され若しくは周囲に巻装された容器に水を貯蔵
して、被破砕物に開設された穴内に配設すること
により該容器の電熱線ヒータ2に所望の時間に通
電することによつて該容器1を破壊せしめ水和反
応が緩慢となつたり、または水和反応が一時的に
停止した膨張性破砕剤スラリー中に膨張性破砕剤
を再消化するための水を補給することにより水和
反応を完全に促進させ、水和膨張圧を再度現出せ
しめることが可能となる。
更に、本発明の第3の実施態様においては、水
を貯蔵した容器は該容器に装着された穿刺体を容
器に貫通させ、該容器に破壊されるように構成さ
れている。即ち本実施態様において使用される容
器1は第2図に示すように、ポリエチレン、ポリ
プロピレン、ポリ塩化ビニール、ナイロン、ポリ
スチレン等の薄いプラスチツク材若しくは厚紙に
より作製された長さ20cm、直径2cm程度の有底の
細長袋により形成されており、該容器1中に水を
注入すると共に牽引用の紐6を結び付けた突刺体
7を内装した後に、注入穴を適宜手段により密封
したものである。該容器1は以上のように構成さ
れているので牽引用の紐6を所望の時間に牽引し
て突刺体7により容器1を内側から破り該容器を
破壊して貯蔵された水を排出させることができ
る。尚、本実施態様において使用される容器の素
材であるプラスチツクの選定に当つては使用され
るプラスチツクの軟化点(融点)は膨張性破砕剤
スラリーの発熱温度よりも高いことが必要である
こと、及び穴内への配置の仕方は上記第2の実施
態様の場合と同様である。
このように突刺体7により容易に破壊される素
材により形成された容器1に水を貯蔵して穴内に
配設するとともに貯水されている容器1に突刺体
7を貫通させることにより所望の時間に破壊せし
めて、膨張力の発現が緩慢になつたりまたは一時
的に停止した膨張性破砕剤スラリー中に、膨張性
破砕剤を再消化するための水を補給することによ
り水和反応を促進させ、水和膨張圧を再度現出せ
しめることが可能となる。尚、本実施態様におい
ては、突刺体7を容器1内部に装着した場合を例
にとり説明したが、容器外部に突刺体を装着した
ものであつても良い。
また、上記各実施態様においては、容器に水を
貯蔵した場合を例にとり説明したが該容器に貯蔵
するものは水に限定されない。即ち、上記各容器
に所定種類及び所定濃度の酸溶液を予め貯蔵して
おき、酸溶液を貯蔵した容器を被破砕物に穿設さ
れた穴内に配置する。そして、被破砕物が破砕さ
れた後に該容器を適宜手段により破壊し、酸溶液
を排出させ、膨張性破砕剤に含まれているアルカ
リ成分を中和させることが可能となり、アルカリ
成分による環境汚染を防止することができる。
更に貯水容器と酸溶液を貯蔵した容器とを共に
穴内に配置し、水和反応が停止したり、緩慢とな
つた時点で、まず貯水容器を破壊し水を排出させ
て水和反応を完全に促進させ、被破砕物の破砕が
終了した時点で、酸溶液を貯蔵した容器を破壊し
膨張性破砕剤中に含まれているアルカリ成分を中
和させることが可能である。
以上のように構成された本発明を以下のとおり
実施した。尚、各実施例につき、夫々、従来方法
による場合との比較を行なつた。
なお、本実施例においては膨張性破砕剤として
S−マイト(住友セメント製商品名)を使用した
が、本発明ではこれに限定されるものではなく例
えばブライスター(小野田セメント製商品名)、
カルシアクリンカー石灰系膨張剤、カルシウムサ
ルフオアルミネート等も利用することができるこ
とは勿論であり、また、容器の材質の選定にあつ
ても何らプラスチツク、紙等に限る必要はまつた
くなく、更に容器の破壊方法も他の適当な方法で
あつてもよく、容器の設置方法、使用する酸の種
類、濃度も場合に応じて任意に選択することがで
きる。
第1実施例
縦300cm、横200cm、高さ150cmに形成されたコ
ンクリート構造物8に、直径40mm、深さ130cmの
穴9を50cm間隔で穿設し、該穴内に水/破砕剤比
27%の膨張性破砕剤S−マイト(住友セメント製
商品名)のスラリー10を充填した。次に、長さ
30cm、直径1.5cmであつて有底ポリエチレン製の
細長袋1aと、この細長袋と同長同径の有底ポリ
プロピレン製の細長袋1bとを用意し、上記ポリ
エチレン製の細長袋1aには水を注入し、一方上
記ポリプロピレン製の細長袋1bには濃度10%の
塩酸溶液を注入し、注入穴を密封した後、これら
の水容器及び酸容器を第3図に示すように穴9上
端部に配設した。その後水容器1a及び酸容器1
bが破壊されるまでの時間、水容器及び酸容器が
破壊された時点におけるスラリー温度、及び亀裂
が発生するまでの時間を測定し、更に、破砕開始
後17時間が経過した時点及び24時間が経過した時
点で、被破砕物8に生じた亀裂の巾を測定した。
また、破砕終了時における膨張性破砕剤S−マイ
ト中に残存する未反応のCaO含有量をX線解折法
を利用して調査し、更に、破砕終了後に膨張性破
砕剤S−マイトの一部を採取してPHを測定した。
尚、膨張性破砕剤S−マイトのPHの測定方法は以
下のとおりである。即ち膨張性破砕剤S−マイト
の一部を採取して揮発性の有機溶媒、例えばエタ
ノール、アセトンで充分に洗浄することにより水
和を停止させ、デシケータ中で乾燥させる。その
後水和反応が停止した膨張性破砕剤S−マイト
1.0gを秤量し、蒸溜水100g中で10分間撹拌
(60rpm)、溶解した後に炉紙5Aで炉過した後に
炉液のPHをPHメーターで測定した。次に、同一条
件下において従来方法により破砕作業を実施し、
これら両者の比較を第2表に示す。[Table] The exothermic temperature of the expandable crushing agent slurry is mainly determined by the type of expandable crushing agent used, the physical characteristics of the material to be crushed (e.g. thermal conductivity, temperature, etc.), the weather during the crushing operation, the temperature, and the mixture. Since it is determined by the amount of water, etc., it is desirable to measure it in advance as a preliminary experiment. Further, in the second embodiment of the present invention, the container storing water is constructed to be destroyed by the heat generated when electricity is applied to a heating wire attached to the container. That is, as shown in FIG. 1, the container 1 used in this embodiment is made of a thin plastic material such as polyethylene, polypropylene, polyvinyl chloride, nylon, polystyrene, or cardboard, and has a length of about 20 cm and a diameter of about 2 cm. The heating wire heater 2 is wrapped around the bottom and/or side surface of the container 1, or the heating wire heater 2 is embedded in the resin forming the container 1. and a power source 3, water is injected into the container 1, and the injection hole is sealed by an appropriate means. This container is suspended by a wire rope 4 via a hook 5 and placed in the hole. Since the present container is constructed as described above, it is possible to destroy the container 1 at a desired time by the heat generated by energizing the electric wire heater 2. In addition, when selecting the material of the plastic used for the above container, the softening point (melting point) of the plastic used and the exothermic temperature of the expandable crushing agent slurry should be taken into consideration. The softening point (melting point) needs to be higher than the exothermic temperature of the hydration-swellable crushing agent slurry. This is because the container storing water will be destroyed by the heat generated when the expandable crushing agent slurry undergoes a hydration reaction. This is because it becomes impossible to destroy it. By storing water in a container in which such an electric wire heater 2 is buried or wrapped around it, and placing it in a hole made in the object to be crushed, the electric wire heater 2 of the container can be heated for a desired time. When the container 1 is energized, the hydration reaction becomes slow or the hydration reaction is temporarily stopped. By replenishing the hydration reaction, it is possible to completely promote the hydration reaction and make the hydration expansion pressure appear again. Furthermore, in a third embodiment of the present invention, the container storing water is configured to be broken into the container by piercing the container with a puncture member attached to the container. That is, as shown in FIG. 2, the container 1 used in this embodiment is a container with a length of about 20 cm and a diameter of about 2 cm, made of a thin plastic material such as polyethylene, polypropylene, polyvinyl chloride, nylon, or polystyrene, or cardboard. It is formed by an elongated bag at the bottom, and after water is injected into the container 1 and a piercing body 7 to which a traction string 6 is tied is placed inside, the injection hole is sealed by an appropriate means. Since the container 1 is constructed as described above, the towing string 6 is pulled at a desired time to break the container 1 from the inside with the pierced body 7, destroying the container and draining the stored water. I can do it. In addition, when selecting the plastic that is the material of the container used in this embodiment, it is necessary that the softening point (melting point) of the plastic used is higher than the exothermic temperature of the expandable crushing agent slurry; The method of arrangement in the hole is the same as in the second embodiment. In this way, water is stored in the container 1 made of a material that is easily destroyed by the piercing body 7, and the water is placed in the hole, and the piercing body 7 is penetrated through the container 1 in which water is stored, at a desired time. Promoting the hydration reaction by replenishing water for re-digesting the expandable crushing agent into the expandable crushing agent slurry whose expansion force has slowed down or temporarily stopped due to destruction, It becomes possible to make the hydration expansion pressure appear again. In addition, in this embodiment, the case where the piercing body 7 is attached to the inside of the container 1 has been explained as an example, but the piercing body may be attached to the outside of the container. Further, in each of the above embodiments, the case where water is stored in a container has been described as an example, but what is stored in the container is not limited to water. That is, an acid solution of a predetermined type and a predetermined concentration is stored in advance in each of the containers, and the container storing the acid solution is placed in a hole drilled in the object to be crushed. After the object to be crushed is crushed, the container is destroyed by appropriate means, the acid solution is discharged, and the alkaline component contained in the expandable crushing agent can be neutralized, resulting in environmental pollution caused by the alkaline component. can be prevented. Furthermore, a water storage container and a container storing an acid solution are placed together in the hole, and when the hydration reaction stops or becomes slow, the water storage container is first destroyed and the water is drained to completely stop the hydration reaction. When the crushing of the material to be crushed is completed, the container storing the acid solution can be destroyed to neutralize the alkaline component contained in the expandable crushing agent. The present invention configured as described above was implemented as follows. For each example, a comparison was made with a conventional method. In this example, S-Mite (trade name, manufactured by Sumitomo Cement) was used as the expandable crushing agent, but the present invention is not limited to this; for example, Blystar (trade name, manufactured by Onoda Cement),
It goes without saying that calcia clinker, lime-based swelling agents, calcium sulfur aluminate, etc. can also be used, and there is no need to limit the selection of container materials to plastic, paper, etc. The method of destroying the acid may also be any other suitable method, and the method of installing the container and the type and concentration of the acid used can be arbitrarily selected depending on the case. First Example Holes 9 with a diameter of 40 mm and a depth of 130 cm are drilled at 50 cm intervals in a concrete structure 8 formed with a length of 300 cm, a width of 200 cm, and a height of 150 cm.
A slurry 10 of 27% expandable crushing agent S-Mite (trade name, manufactured by Sumitomo Cement) was filled. Next, the length
Prepare an elongated polyethylene bag 1a with a diameter of 30 cm and 1.5 cm, and a polypropylene elongated bag 1b with a bottom and the same length and diameter as the elongated bag.The polyethylene elongated bag 1a is filled with water. On the other hand, a hydrochloric acid solution with a concentration of 10% is injected into the elongated polypropylene bag 1b, and after sealing the injection hole, the water container and acid container are inserted into the upper end of the hole 9 as shown in FIG. It was placed in Then water container 1a and acid container 1
Measure the time until b is destroyed, the slurry temperature at the time when the water container and acid container are destroyed, and the time until cracks occur, and furthermore, measure the time taken 17 hours and 24 hours after the start of crushing. After the elapse of time, the width of the cracks formed in the object 8 to be crushed was measured.
In addition, we used X-ray analysis to investigate the unreacted CaO content remaining in the expandable crushing agent S-Mite at the end of crushing, and A sample was taken and the pH was measured.
The method for measuring the pH of the expandable crushing agent S-Mite is as follows. That is, a part of the expandable crushing agent S-Mite is collected, thoroughly washed with a volatile organic solvent such as ethanol or acetone to stop hydration, and dried in a desiccator. Expandable crushing agent S-Mite, after which the hydration reaction stopped
1.0 g was weighed out, stirred in 100 g of distilled water for 10 minutes (60 rpm), dissolved, filtered through furnace paper 5A, and the pH of the furnace liquid was measured using a PH meter. Next, crushing work is carried out using the conventional method under the same conditions,
A comparison between these two is shown in Table 2.
【表】
第2実施例
縦150cm、横150cm、高さ150cmに形成されたコ
ンクリート構造物8に直径60mm、深さ120cmの穴
9を40cm間隔で2本穿設し、該穴9内に水/破砕
剤比25%の膨張性破砕剤特殊S−マイト(スラリ
ー状態における発熱温度が100℃に達する時間が
35分に調整されたS−マイト)のスラリー10を
充填し、長さ20cm、直径2.5cmであつて有底のポ
リスチレン製の細長袋により形成され、その側面
の樹脂層間に電熱線ヒータ2を埋込んだ細長い袋
1cを2つ用意しこの細長袋の一方1cには水
を、他方1dには濃度15%の硫酸溶液を注入し、
双方の細長袋1c,1dの注入穴を密封した後こ
れら水容器1c及び酸容器1dを第4図に示すよ
うに穴9上端部に配設した。また、該スラリー1
0中央部に直径5mmの塩化ビニール製パイプ11
を、その下端が上記スラリー10に埋没すると共
に上端が穴9より外部に突出するように挿入し
た。この塩化ビニール製パイプ11は水和熱を原
因とする混練水の蒸発を排出させるものであり、
噴出現象の防止に寄与するものである。更にジエ
ツトセメント(住友セメント製商品名)及び砂か
ら成る超速硬性モルタル12により上記パイプ1
1の周囲に10cmの深さでタンピングした。その後
膨張性破砕剤である特殊S−マイトを充填した後
25分が経過した時点で水容器1cの電熱線ヒータ
2に通電し、発生する熱によつて該水容器1cを
破壊せしめ、末反応の膨張性破砕剤を再反応、再
消化させるための水を補給し、その後亀裂の発生
状況等を観察し、膨張性破砕剤である特殊S−マ
イト中に残存する未反応のCaO含有量をX線解折
方法を利用して調査した。
一方、膨張性破砕剤である特殊S−マイトを充
填した後8時間が経過した時点で酸容器1dの電
熱線ヒータ2に通電し、発生する熱により該容器
1dを破壊せしめて、破砕が終了した膨張性破砕
剤である特殊S−マイトのアルカリを中和させる
と共に中和された膨張性破砕剤である特殊S−マ
イトの一部を採取してそのPHを測定したものであ
る。次に、同一条件下において従来方法により破
砕作業を実施し、これら両者の比較を表3に示
す。[Table] 2nd Example Two holes 9 with a diameter of 60 mm and a depth of 120 cm are bored at 40 cm intervals in a concrete structure 8 formed with a length of 150 cm, a width of 150 cm, and a height of 150 cm, and water is poured into the holes 9. / Expandable crushing agent special S-Mite with a crushing agent ratio of 25% (time to reach exothermic temperature of 100℃ in slurry state)
A slender polystyrene bag with a length of 20 cm and a diameter of 2.5 cm and a bottom is filled with a slurry 10 of S-Mite prepared for 35 minutes, and an electric wire heater 2 is installed between the resin layers on the side of the bag. Two embedded elongated bags 1c are prepared, water is poured into one of the elongated bags 1c, and a sulfuric acid solution with a concentration of 15% is poured into the other 1d.
After the injection holes of both the elongated bags 1c and 1d were sealed, the water container 1c and the acid container 1d were placed at the upper end of the hole 9 as shown in FIG. In addition, the slurry 1
0 PVC pipe 11 with a diameter of 5 mm in the center
was inserted so that its lower end was buried in the slurry 10 and its upper end protruded outside from the hole 9. This pipe 11 made of vinyl chloride discharges evaporation of kneading water caused by heat of hydration.
This contributes to the prevention of eruption phenomena. Furthermore, the pipe 1 is molded with ultra-fast hardening mortar 12 made of jet cement (trade name manufactured by Sumitomo Cement) and sand.
Tamping was performed around 1 to a depth of 10 cm. After filling with special S-Mite, which is an expandable crushing agent,
When 25 minutes have elapsed, the electric wire heater 2 of the water container 1c is energized, and the generated heat destroys the water container 1c. After that, the occurrence of cracks was observed, and the content of unreacted CaO remaining in the special S-Mite, which is an expansive crushing agent, was investigated using an X-ray analysis method. On the other hand, when 8 hours have passed after filling the special S-Mite, which is an expandable crushing agent, the electric wire heater 2 of the acid container 1d is energized, and the generated heat destroys the container 1d, completing the crushing. The alkali of Special S-Mite, which is an expandable crushing agent, was neutralized, and a part of the neutralized Special S-Mite, which is an expandable crushing agent, was collected and its PH was measured. Next, a crushing operation was carried out using the conventional method under the same conditions, and a comparison between the two is shown in Table 3.
【表】
第3実施例
輝緑凝灰岩8に直径150mm、深さ6mの穴9を
2.5m間隔で穿設し該穴9内に水/破砕剤比25%
の膨張性破砕剤S−マイトのスラリー10を充填
した。次に長さ10cm、直径3cmであつて有底のポ
リ塩化ビニール製の細長袋1eを30本用意し、こ
れらの袋に水を注入し一方、同長同径であつて有
底のポリスチレン製細長袋1fを30本用意しこれ
らの袋1e,1fに濃度20%の塩酸溶液を注入
し、これらの2つの細長袋1e,1fの注入穴を
密封した後、第5図に示すように穴9内に配置し
た。更に、ジエツトセメント及び砂から成る超速
硬性モルタル12により該穴9の上端部10cmの深
さ範囲をタンピングした。その後、亀裂の発生状
況等を観察すると共に膨張性破砕剤S−マイト中
に残存する未反応のCaO含有量をX線解折法に利
用して調査し、更に破砕作業終了後に膨張性破砕
剤S−マイトの一部を採取してPHを測定した。次
に同一条件下において従来方法により破砕作業を
実施しこれら両者の比較を表4に示す。[Table] Third Example A hole 9 with a diameter of 150 mm and a depth of 6 m is made in the diabase tuff 8.
Drill holes at 2.5m intervals and fill the holes 9 with a water/crushing agent ratio of 25%.
A slurry 10 of the expandable crushing agent S-mite was filled. Next, prepare 30 elongated bags 1e made of polyvinyl chloride with a length of 10 cm and a diameter of 3 cm with a bottom, and fill these bags with water. Prepare 30 elongated bags 1f, inject hydrochloric acid solution with a concentration of 20% into these bags 1e and 1f, seal the injection holes in these two elongated bags 1e and 1f, and then open the holes as shown in Figure 5. It was placed within 9. Further, the upper end of the hole 9 was tamped to a depth of 10 cm using an ultra-fast hardening mortar 12 made of jet cement and sand. After that, we observed the occurrence of cracks, etc., and investigated the unreacted CaO content remaining in the expandable crushing agent S-Mite using X-ray analysis. A portion of S-mite was collected and its pH was measured. Next, a crushing operation was carried out using the conventional method under the same conditions, and a comparison between the two is shown in Table 4.
【表】【table】
【表】
第4実施例
縦300cm、横200cm、高さ200cmに形成されたコ
ンクリート構造物8に直径5cm、深さ170cmの穴
9を50cm間隔で穿設し、該穴9内に水/破砕剤比
27%の膨張性破砕剤S−マイトのスラリー10を
充填し、長さ30cm、直径2cmであつて有底のポリ
スチレン製の細長袋を2つ用意し、これら2つの
容器の一方の容器1gには水をまた他方の容器1
hには濃度10%の塩酸溶液を注入すると共に牽引
用の紐6を結び付けた突刺体7を容器に内装させ
た後に、注入穴を適宜手段により密封し、これら
の容器1g,1hを上記穴9内に配設した。以
後、膨張性破砕剤S−マイトスラリー10を充填
した後、5時間経過した時点で水容器1gを突刺
体7に結び付けた牽引用の紐6を牽引することに
より突刺体7を水容器1gに貫通させて破壊せし
め、未反応の膨張性破砕剤を再反応、消化させる
ための水を補給し、その後の亀裂の発生状況等を
観察し膨張性破砕剤S−マイト中に残存する未反
応のCaO含有量をX線解折法を利用して調査し
た。また、膨張性破砕剤充填後18時間が経過した
時点で酸容器1hを水容器1g同様に突刺体7に
結び付けた牽引用の紐6を牽引することにより突
刺体7を酸容器1hに貫通させて破壊せしめ、貯
蔵していた酸容液を排出させ破砕が終了した膨張
性破砕剤S−マイトのアルカリを中和させた後、
その一部を採取してPHを測定した。一方、同一条
件下において従来方法により破砕作業を実施しこ
れら両者の比較を表5に示す。[Table] Fourth Example Holes 9 with a diameter of 5 cm and a depth of 170 cm are drilled at 50 cm intervals in a concrete structure 8 formed with a length of 300 cm, a width of 200 cm, and a height of 200 cm, and water/fracture is poured into the holes 9. drug ratio
Prepare two elongated polystyrene bags with a length of 30 cm and a diameter of 2 cm, each with a bottom, filled with slurry 10 of the 27% expandable crushing agent S-Mite, and add 1 g to one of these two containers. is the water in the other container 1
After injecting a hydrochloric acid solution with a concentration of 10% into the container h and placing the piercing body 7 to which the traction string 6 is tied inside the container, the injection hole is sealed by an appropriate means, and the containers 1g and 1h are inserted into the hole described above. It was placed within 9. Thereafter, after 5 hours have elapsed after filling the expandable crushing agent S-mite slurry 10, the traction string 6 tied to the pierced body 7 is pulled to turn the pierced body 7 into a water container of 1 g. The unreacted expandable crushing agent is penetrated and destroyed, and water is replenished to re-react and extinguish the unreacted expandable crushing agent. Afterwards, the occurrence of cracks, etc. is observed, and the unreacted crushing agent remaining in the expandable crusher S-Mite is The CaO content was investigated using X-ray diffraction method. In addition, when 18 hours have passed after filling the expandable crushing agent, the acid container 1h is penetrated into the acid container 1h by pulling the traction string 6 tied to the piercing body 7 in the same way as the water container 1g. After discharging the stored acid solution and neutralizing the alkali of the expanded crushing agent S-Mite,
A portion of it was collected and its pH was measured. On the other hand, crushing work was carried out using the conventional method under the same conditions, and a comparison between the two is shown in Table 5.
【表】
以上表2から表5に示すように、本発明に係る
各実施例によれば、従来方法による破砕作業と比
較した場合、破砕開始後の膨張性破砕剤中に残存
する未反応のCaO含有量は著しく少なくなり、亀
裂巾も大きいことが判明した。このことは膨張性
破砕剤スラリー中からの混練水の蒸発により水和
膨張圧の発現が緩慢となつたり、または一時的に
停止した膨張性破砕剤に未反応の膨張性破砕剤の
再反応、再消化のための水を補給することによ
り、膨張性破砕剤が有する膨張圧を継続的且つ効
率的に発現させることが可能となることを示す。
更に、上記各実施例によれば、破砕終了時の膨張
性破砕剤のPH値は従来方法に比較して小さいこと
が判明した。このことは破砕作業が終了した膨張
性破砕剤に酸溶液を添加することにより、破砕が
終了した膨張性破砕剤のアルカリを所望の時間内
に中和することが可能であると共に施工場所近く
でのアルカリ汚染防止が可能となることを示すも
のである。
本発明は以上のような構成を有するものである
ため、未反応の膨張性破砕剤を任意の時間に再反
応、再消化させるための補給水を穴内部に貯蔵す
ることが可能となるため膨張性破砕剤を充分に再
反応、再消化せしめ膨張性破砕剤の有する膨張圧
を継続的に発現せしめることができ、岩石、地
山、コンクリート構造物等の脆性物体の被破砕物
を迅速且つ効率的に破砕することが可能となる。
また、破砕作業に未反応の膨張性破砕剤を再消
化、再反応させるための再注水作業を行なう必要
がなくなるため、安全且つ円滑に破砕作業を行な
うことができる、という効果を奏する。[Table] As shown in Tables 2 to 5 above, according to each of the examples according to the present invention, when compared with the crushing operation by the conventional method, the unreacted amount remaining in the expandable crushing agent after the start of crushing was It was found that the CaO content was significantly reduced and the crack width was also large. This means that the development of hydration expansion pressure becomes slow due to evaporation of the kneading water from the expandable crushing agent slurry, or that the unreacted expandable crushing agent reacts with the temporarily stopped expandable crushing agent. This shows that by replenishing water for re-digestion, it is possible to continuously and efficiently develop the swelling pressure of the swelling crushing agent.
Furthermore, according to each of the above examples, it was found that the PH value of the expandable crushing agent at the end of crushing was smaller than that of the conventional method. This means that by adding an acid solution to the expansible crushing agent after crushing work, it is possible to neutralize the alkali in the expansible crushing agent after crushing within the desired time, and it is also possible to neutralize the alkali in the expansible crushing agent after crushing has been completed, and to remove the alkali from the expansible crushing agent near the construction site. This shows that it is possible to prevent alkaline contamination. Since the present invention has the above configuration, it is possible to store make-up water inside the hole for re-reacting and re-digesting the unreacted expandable crushing agent at any time. It is possible to sufficiently re-react and re-digest the expansible crushing agent and to continuously develop the expansion pressure of the expansible crushing agent, allowing for rapid and efficient crushing of brittle objects such as rocks, earth, concrete structures, etc. It becomes possible to crush the material.
Furthermore, since there is no need to re-inject water in order to re-digest and re-react the unreacted expandable crushing agent during the crushing operation, there is an effect that the crushing operation can be carried out safely and smoothly.
第1図は電熱線ヒータが埋設された水または酸
溶液を貯蔵する容器を示す平面図、第2図は突刺
体を内装した水または酸溶液を貯蔵する容器を示
す断面図、第3図乃至第6図は本発明に係る破砕
方法による被破砕物の破砕状況を示す断面図であ
る。
1……容器、1a,1c,1e,1g……水容
器(細長袋)、1b,1d,1f,1h……酸容
器(細長袋)、2……電熱線(ヒータ)、7……突
刺体。
Fig. 1 is a plan view showing a container for storing water or acid solution in which an electric wire heater is embedded, Fig. 2 is a sectional view showing a container for storing water or acid solution equipped with a piercing body, and Figs. FIG. 6 is a sectional view showing the state of crushing of an object to be crushed by the crushing method according to the present invention. 1... Container, 1a, 1c, 1e, 1g... Water container (elongated bag), 1b, 1d, 1f, 1h... Acid container (elongated bag), 2... Heating wire (heater), 7... Pierce body.
Claims (1)
しコンクリート構造物及び岩石等の脆性物体を破
壊する破壊工法において、貯水した容器を被破砕
物に開設された穴内の膨張性破砕剤スラリー中に
配置し、水和膨張圧低下時に該容器を破壊するこ
とにより、該容器内の水を排出させ、水和膨張圧
を再度現出せしめることにより、被破砕物を破砕
することを特徴とする破壊工法。 2 上記容器は膨張性破砕剤スラリーの水和反応
により発する熱によつて破壊されることを特徴と
する特許請求の範囲第1項記載の破壊工法。 3 上記容器には電熱線が装着されており、該電
熱線に通電した場合に発生する熱により該容器を
破壊することを特徴とする特許請求の範囲第1項
記載の破壊工法。 4 上記容器には突刺体が装着されており、該突
刺体を容器に貫通させて該容器を破壊することを
特徴とする特許請求の範囲第1項記載の破壊工
法。[Claims] 1. In a destruction method that uses hydration expansion pressure generated by reaction with water to destroy brittle objects such as concrete structures and rocks, a container containing water is placed in a hole made in the object to be crushed. By disposing an expandable crushing agent in a slurry and destroying the container when the hydration expansion pressure decreases, the water in the container is drained and the hydration expansion pressure is made to appear again, thereby crushing the object to be crushed. A destructive construction method characterized by: 2. The destruction method according to claim 1, wherein the container is destroyed by heat generated by the hydration reaction of the expandable crushing agent slurry. 3. The method of destruction according to claim 1, wherein a heating wire is attached to the container, and the container is destroyed by the heat generated when the heating wire is energized. 4. The method of destruction according to claim 1, characterized in that a piercing body is attached to the container, and the piercing body is penetrated into the container to destroy the container.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20278883A JPS6095076A (en) | 1983-10-31 | 1983-10-31 | Crushing construction method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20278883A JPS6095076A (en) | 1983-10-31 | 1983-10-31 | Crushing construction method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6095076A JPS6095076A (en) | 1985-05-28 |
| JPH0340185B2 true JPH0340185B2 (en) | 1991-06-18 |
Family
ID=16463199
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP20278883A Granted JPS6095076A (en) | 1983-10-31 | 1983-10-31 | Crushing construction method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6095076A (en) |
-
1983
- 1983-10-31 JP JP20278883A patent/JPS6095076A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6095076A (en) | 1985-05-28 |
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