JPS58154779A - Breaking agent for brittle substance - Google Patents
Breaking agent for brittle substanceInfo
- Publication number
- JPS58154779A JPS58154779A JP57037653A JP3765382A JPS58154779A JP S58154779 A JPS58154779 A JP S58154779A JP 57037653 A JP57037653 A JP 57037653A JP 3765382 A JP3765382 A JP 3765382A JP S58154779 A JPS58154779 A JP S58154779A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- cement
- agent
- crushing
- hydration
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000126 substance Substances 0.000 title claims abstract description 14
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 21
- 239000004568 cement Substances 0.000 claims abstract description 13
- 239000013078 crystal Substances 0.000 claims abstract description 10
- 239000000843 powder Substances 0.000 claims abstract description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 20
- 239000000463 material Substances 0.000 claims description 15
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims description 13
- 235000011941 Tilia x europaea Nutrition 0.000 claims description 13
- 239000004571 lime Substances 0.000 claims description 13
- 239000003638 chemical reducing agent Substances 0.000 claims description 8
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 2
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 abstract description 32
- 239000000292 calcium oxide Substances 0.000 abstract description 16
- 235000012255 calcium oxide Nutrition 0.000 abstract description 16
- 238000006703 hydration reaction Methods 0.000 abstract description 12
- 230000036571 hydration Effects 0.000 abstract description 9
- 239000002002 slurry Substances 0.000 abstract description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract description 6
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 abstract description 6
- 239000011398 Portland cement Substances 0.000 abstract description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 abstract description 3
- 235000010216 calcium carbonate Nutrition 0.000 abstract description 3
- RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 abstract description 2
- 239000004567 concrete Substances 0.000 abstract description 2
- 239000011435 rock Substances 0.000 abstract description 2
- 239000012024 dehydrating agents Substances 0.000 abstract 2
- 239000003112 inhibitor Substances 0.000 description 9
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 235000019738 Limestone Nutrition 0.000 description 2
- 229910052925 anhydrite Inorganic materials 0.000 description 2
- 229910001570 bauxite Inorganic materials 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000010304 firing Methods 0.000 description 2
- 239000006028 limestone Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- 230000009257 reactivity Effects 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
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 229910000975 Carbon steel Inorganic materials 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- XFWJKVMFIVXPKK-UHFFFAOYSA-N calcium;oxido(oxo)alumane Chemical compound [Ca+2].[O-][Al]=O.[O-][Al]=O XFWJKVMFIVXPKK-UHFFFAOYSA-N 0.000 description 1
- 239000010962 carbon steel Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000001079 digestive effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229910052806 inorganic carbonate Inorganic materials 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 235000011083 sodium citrates Nutrition 0.000 description 1
- 239000000176 sodium gluconate Substances 0.000 description 1
- 235000012207 sodium gluconate Nutrition 0.000 description 1
- 229940005574 sodium gluconate Drugs 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Landscapes
- Disintegrating Or Milling (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、岩石、コンクリート等の脆性物体の破砕剤に
関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a crushing agent for brittle objects such as rocks and concrete.
従来から、脆性物体を破砕する方法としては、例えは特
開昭56−6705帰公報に記載されているように生石
灰を含有するものが多く提案されている。その生石灰の
品質としては、−yにCaOの純度の高いこと、および
水との反応が遅いことが要求されている。この水との反
応性は、生石灰を生産する時の石灰石の焼成条件に依存
し、低温度かつ短時間で焼成して得られる軟焼品は、水
との反応が速いので、破砕剤として用いる場合は、直ち
に水利膨張し材料ペーストの軟度が急激に低下し作業が
困難となる。Conventionally, as a method for crushing brittle objects, many methods containing quicklime have been proposed, for example, as described in Japanese Unexamined Patent Publication No. 56-6705. As for the quality of the quicklime, -y is required to have high purity of CaO and slow reaction with water. This reactivity with water depends on the firing conditions of the limestone when producing quicklime, and soft-burnt products obtained by firing at low temperatures and in a short time react quickly with water, so they are used as crushing agents. If this occurs, the material paste will immediately expand due to water use, and the softness of the material paste will drop rapidly, making it difficult to work.
本発明者は、このような生石灰を主材とする破砕剤の欠
点を解決する目的で種々検討した結果、CaO粒子表面
をCaCO3薄膜層でコーテングしたものを主材とする
混合物を使用すれば、25C以上の夏場においても容易
に水利反応をコントロールすることができるので、十分
に破砕できることを見い出し本発明を完成したものであ
る。As a result of various studies aimed at solving the shortcomings of such crushing agents mainly composed of quicklime, the present inventor found that if a mixture containing mainly CaO particles coated with a CaCO3 thin film layer is used, We have completed the present invention by discovering that the water utilization reaction can be easily controlled even in the summer when temperatures are above 25C, allowing for sufficient crushing.
すなわち、本発明は、結晶径が10μ未満である軟焼生
石灰粉末の表面炭酸化物50〜95重量%と水硬性物質
50〜5重量%からなる主材100重量部に対し、セメ
ント減水剤0.5〜3重量部を含有させてなる脆性物体
の破砕剤である。That is, according to the present invention, 0.00 parts by weight of a cement water reducing agent is added to 100 parts by weight of a main material consisting of 50 to 95% by weight of surface carbonates and 50 to 5% by weight of hydraulic substances of soft calcined quicklime powder having a crystal diameter of less than 10 μm. This is a crushing agent for brittle objects containing 5 to 3 parts by weight.
以下詳しく本発明を説明する。The present invention will be explained in detail below.
本発明は、結晶径10μ未満である軟焼生石灰の表面炭
酸化物、水硬性物質及びセメント減水剤と必要に応じて
セメント水利抑制剤とを含有するもので、結晶径10μ
未満の軟焼生石灰の表面炭酸化物50〜95重1%と水
硬性物質50〜5重量%からなるものを主材とするもの
である。このような炭酸化処理した軟焼生石灰を主成分
とすることにより、水和抑制剤の添加をとくに必要とし
ないで水和反応を容易にコントロールすることができる
という利点がある。The present invention contains a surface carbonate of soft burnt lime having a crystal size of less than 10 μm, a hydraulic substance, a cement water reducing agent, and if necessary, a cement water usage inhibitor.
The main material is 50 to 95 1% by weight of surface carbonated soft burnt lime and 50 to 5 % by weight of hydraulic substances. By using carbonated soft calcined lime as the main component, there is an advantage that the hydration reaction can be easily controlled without the need for adding a hydration inhibitor.
軟焼生石灰粉末の炭酸化程度は、それを大きくする程、
生石灰の水和反応を抑制することができるが、その反面
、膨張力が小さくなるので、軟焼生石灰粉末表面を炭酸
カルシウムで薄くコーティングされる程度にするのが望
ましい。そのようなものを得るには、石灰石を焼蜘して
得られた結晶径10μ未満の軟焼生石灰を粉砕して容器
に入れ、C02カスと0.5〜10時間程度接触すれば
よい。The degree of carbonation of soft calcined lime powder increases as it increases.
It is possible to suppress the hydration reaction of quicklime, but on the other hand, the swelling force is reduced, so it is desirable that the surface of the soft-burned quicklime powder be coated thinly with calcium carbonate. To obtain such a product, soft calcined lime with a crystal diameter of less than 10 μm obtained by calcining limestone is crushed, placed in a container, and contacted with CO2 scum for about 0.5 to 10 hours.
本発明において、軟焼生石灰の結晶径を10μ未満に限
定した理由は、結晶径が10μ以上の硬焼生石灰であっ
ては、生石灰表面の活性が殺されているため、炭酸化し
にくいばかりでなく、炭酸化しても水和反応が著しく遅
くなるからである。In the present invention, the reason why the crystal size of soft calcined lime is limited to less than 10μ is that hard calcined lime with a crystal size of 10μ or more is not only difficult to carbonate, but also because the activity of the lime surface is destroyed. This is because even if carbonated, the hydration reaction is significantly slowed down.
水硬性物質としては、普通ポルトランドセメント等の各
種ポルトランドセメント、超速硬セメントおよびアルミ
ナセメント、さらには石灰とボーキサイトを所定量配合
して1ろ00C〜1600 Cで溶融後、冷却すること
によって得られる、例えばCl2A7、C3A、 CA
、 C,、A7CaF2等のカルシウムアルミネート単
独又はこれらと無水石膏との混合物のようなものがあげ
られる。Hydraulic substances include various types of Portland cement such as ordinary Portland cement, ultra-fast hardening cement, alumina cement, and even lime and bauxite, which can be obtained by blending a predetermined amount of lime and bauxite, melting at 100C to 1600C, and then cooling. For example Cl2A7, C3A, CA
, C, , A7CaF2 alone or a mixture of these and anhydrite can be mentioned.
本発明において、主材の割合を前記のように特定した理
由は、結晶径10μ未満の軟焼生石灰粉末の表面炭酸化
物が50重量%未満では、膨張圧が小さくなって破砕に
時間がかかりすぎ、また、95重歇%を超えると生石灰
の消化反応性が大きくなり、その破砕剤をスラリーとし
て脆性物体の穿孔中に注入しても、注入口から噴出し膨
張圧は皮砕幻となりにくいからである。好ましい割合は
、結晶径10μ未満の軟焼生石灰粉末の表面炭酸化物5
0〜70重徽%、水硬性物質50−30重量%である。In the present invention, the reason why the ratio of the main material is specified as described above is that if the surface carbonate of soft calcined lime powder with a crystal diameter of less than 10μ is less than 50% by weight, the expansion pressure becomes small and crushing takes too much time. In addition, if the content exceeds 95%, the digestive reactivity of quicklime increases, and even if the crushing agent is injected into a hole in a brittle object as a slurry, the expansion pressure ejected from the injection port is unlikely to cause skin crushing. It is. A preferable ratio is surface carbonate of soft calcined lime powder with a crystal diameter of less than 10μ.
0-70% by weight, and 50-30% by weight of hydraulic material.
すなイつち、本発明で限定された主材を用いた破砕剤ス
ラリーを脆性物体の穿孔中に注入しても、注入口より噴
出することなく大きな膨張圧を得ることができる。これ
は、前記水硬性物質の自硬性によって生じた破砕剤水和
物と注入口となる孔の壁面との間に大きな摩擦力を生じ
噴出が防止されるからである。In other words, even if the crushing agent slurry using the main material limited in the present invention is injected into the perforation of a brittle object, a large expansion pressure can be obtained without ejecting from the injection port. This is because a large frictional force is generated between the crushing agent hydrate produced by the self-hardening property of the hydraulic substance and the wall surface of the hole serving as the injection port, thereby preventing ejection.
本発明の主材を構成する炭酸化処理した軟焼生石灰と水
硬性物質の粒度は、それぞれブレーン値で2000〜5
000crn2//1程度のものを用い、破砕剤とした
場合には2500〜50006n!/Pとなるように調
整すればよい。これらの成分の粒度が粗粉末すぎると材
料分離を生じ、また、微粉末すぎると膨張圧が小さくな
るので好ましくない。The particle size of the carbonated soft calcined lime and the hydraulic substance that constitute the main material of the present invention is 2000 to 5 in Blaine value, respectively.
000crn2//1 is used as a crushing agent, it is 2500 to 50006n! /P. If the particle size of these components is too coarse, material separation will occur, and if the particle size is too fine, the expansion pressure will become low, which is not preferable.
本発明は、以上の主材100重量部にセメント減水剤0
.5〜6重量部を存在させたものである。In the present invention, 100 parts by weight of the above main material and no cement water reducing agent are added.
.. 5 to 6 parts by weight are present.
セメント減水剤としては、いわゆる高性能減水剤とよば
れているものが好ましく、具体的には、リグニンスルホ
ン酸塩系、水溶性メラミン樹脂系、高級多価アルコール
のスルホン酸塩系、β−ナフタリンスルホン酸塩ホルマ
リン縮合物系などの1(5)
種以上が使用される。これを主材1[]01重量に対し
0.5〜3重量部を配合すれば、流動性を大幅に改良し
水比を減少させることができるので、膨張圧が増大し、
−14強力にすることができる。すなわち、セメント減
・水剤の割合が0,5重量部未満では、このような効果
は小さく、また、6重量部をこえても減水効果はそれ程
向上しないので不経済である。好ましいセメント減水剤
の割合は1〜2重量部である。The cement water reducing agent is preferably a so-called high-performance water reducing agent, and specifically, lignin sulfonate type, water-soluble melamine resin type, higher polyhydric alcohol sulfonate type, and β-naphthalene. One (5) or more species such as sulfonate formalin condensate systems are used. By adding 0.5 to 3 parts by weight of this to the weight of the main material 1[]01, the fluidity can be greatly improved and the water ratio can be reduced, increasing the expansion pressure.
-14 Can be made powerful. That is, if the proportion of the cement reduction/water agent is less than 0.5 parts by weight, such an effect will be small, and if it exceeds 6 parts by weight, the water reduction effect will not improve significantly, which is uneconomical. The preferred proportion of cement water reducer is 1 to 2 parts by weight.
本発明の破砕剤は、とくに水和抑制剤を添加する必要は
ないが、ときには主材100重責部に対し多くても2重
量部のそれを使用してもよい。その水和抑制剤としては
、一般に知られているもの、例えば炭酸カリウム、炭酸
ソーダなどの無機炭酸塩類、クエン酸、酒石酸、クエン
酸ソーダ、グルコン酸ソーダなどの有機ヒドロキシカル
ボン酸又はその塩類から選ばれた1種以上があげられる
。Although it is not necessary to add a hydration inhibitor to the crushing agent of the present invention, it may be used in an amount of at most 2 parts by weight per 100 parts by weight of the main material. The hydration inhibitor is selected from commonly known ones, such as inorganic carbonates such as potassium carbonate and soda carbonate, and organic hydroxycarboxylic acids or their salts such as citric acid, tartaric acid, sodium citrate, and sodium gluconate. One or more types can be listed.
以上の本発明の破砕剤を使用すれば、水利抑制剤を必要
としないで、流動性に優れ、かつ高温に−おいても高い
膨張圧を示すスラリーを調合できる(6)
ので、夏場での脆性物体を短時間に破砕できるという効
果を発現する。すなわち、従来の破砕剤では、少くとも
5重量部の水和抑制剤を必要としたが、それでも夏場に
おいては十分な破砕工事ができなかった。しかし、本発
明品では、水和抑制剤を必要としないでそれを可能とな
ったものでちる。By using the above-described crushing agent of the present invention, it is possible to prepare a slurry that has excellent fluidity and exhibits high expansion pressure even at high temperatures without requiring a water usage inhibitor (6). It has the effect of crushing brittle objects in a short time. That is, the conventional crushing agent required at least 5 parts by weight of a hydration inhibitor, but even then, sufficient crushing work could not be carried out in the summer. However, the product of the present invention makes this possible without requiring a hydration inhibitor.
以下、実施例をあげてさらに詳しく説明する。Hereinafter, the present invention will be explained in more detail with reference to examples.
実施例1
結晶径10μ未満の軟焼生石灰をブレーン比表面積ろ、
000 cm2/g−に粉砕し、これをCO2カスと
1.5時間接触させて、表面炭酸化処理した生石灰粉末
を得た。このもの60重量%と、12CaO・71Q2
0.の組成を有する非晶質カルシウムアルミネートと■
型無水石膏の等重量混合物からなる水硬性物質40重量
%とからなる主材100重量部に対し、リグニンスルホ
ン酸カルシウムを主成分とする市販の七メント減水剤(
商品名「ウルトラジン」)1重量部を配合して破砕剤と
した。この破砕剤100重量部に65重着部の水を混合
してスラリーとし、室温20 Cにおける可使時間を測
定したところ14分であり、また、室温25 Cにおけ
る12時間の膨張圧を測定したところ4400 t/m
2であった。Example 1 Soft calcined lime with a crystal diameter of less than 10μ was subjected to Blaine specific surface area filtering.
000 cm2/g- and brought into contact with CO2 scum for 1.5 hours to obtain quicklime powder whose surface was carbonated. This stuff is 60% by weight and 12CaO 71Q2
0. Amorphous calcium aluminate with the composition of ■
To 100 parts by weight of the main material consisting of 40% by weight of a hydraulic substance consisting of an equal weight mixture of molded anhydrite, a commercially available 7-ment water reducing agent (based on calcium ligninsulfonate) was added.
1 part by weight (trade name: "Ultra Gin") was blended to prepare a crushing agent. 100 parts by weight of this crushing agent was mixed with 65 parts of water to form a slurry, and the pot life at a room temperature of 20 C was measured to be 14 minutes, and the expansion pressure was measured at a room temperature of 25 C for 12 hours. Tokoro 4400 t/m
It was 2.
なお、可使時間は、注水から流動性がなくなるまでの所
要時間を測定した。また、膨張圧は、内径66醪、高さ
600 mの配管用炭素鋼鋼管の底部に鋼板を熔接し、
その表面の高さ中央部にゲージ長10mのペーパースト
レインゲージを円周方向向に貼付した鋼管内にスラリー
を注入し、放置したときの鋼管の歪みから算出した。Note that the pot life was determined by measuring the time required from pouring water until the fluidity disappeared. In addition, the expansion pressure was determined by welding a steel plate to the bottom of a carbon steel pipe for piping with an inner diameter of 66 mm and a height of 600 m.
The slurry was injected into a steel pipe to which a paper strain gauge with a gauge length of 10 m was attached in the circumferential direction at the center of the height of the surface, and the strain was calculated from the strain of the steel pipe when it was left standing.
実施例2
実施例1において、破砕剤にさらに1重量部の水和抑制
剤を添加したものを用いたところ、可使時間は50分て
あり、膨張圧は4270 t/m2であったO
なお、使用した水和抑制剤は、炭酸カリウム冗重量%、
クルコン酸ソータ13重量%、クエン酸17重量%の混
合物である。Example 2 In Example 1, when 1 part by weight of a hydration inhibitor was added to the crushing agent, the pot life was 50 minutes and the expansion pressure was 4270 t/m2. , the hydration inhibitor used was potassium carbonate redundant weight%,
It is a mixture of 13% by weight of curconic acid sorter and 17% by weight of citric acid.
実施例6
実施例2において、主材の組成割合を変えた以外は、同
様にして可使時間と膨張圧を測定した。Example 6 The pot life and expansion pressure were measured in the same manner as in Example 2, except that the composition ratio of the main material was changed.
その結果を第1表に示す。The results are shown in Table 1.
第 1 表
触時間を変えた以外は、同様にして可使時間と膨張圧を
測定した。その結果を第2表に示す。なお、該表には、
軟焼生石灰に含まれるCO2量の分析結果も示した。1. Pot life and expansion pressure were measured in the same manner except that the surface contact time was changed. The results are shown in Table 2. In addition, in this table,
The results of an analysis of the amount of CO2 contained in soft burnt lime are also shown.
(9)
実施例5
破砕剤を性能評価するため、直径15m、高さ6゜αの
モルタル硬化体(圧縮強度506 ktf/cm2、引
張強度62 ktf/cmりの中央部に直径28 ta
xの孔を貫通し、そこへ実施例1〜4で調合したスラリ
ーを注入して25 C室温に放置した。その結果、破砕
に要した時間は、実施例1の破砕剤では100分であり
、また、他の破砕剤では第1表〜第2表に示した通りで
あった。(9) Example 5 In order to evaluate the performance of the crushing agent, a hardened mortar body with a diameter of 15 m and a height of 6° α (compressive strength of 506 ktf/cm2, tensile strength of 62 ktf/cm) was prepared with a diameter of 28 ta in the center.
The slurry prepared in Examples 1 to 4 was injected into the hole x and left at room temperature of 25C. As a result, the time required for crushing was 100 minutes for the crushing agent of Example 1, and the time required for crushing was as shown in Tables 1 and 2 for the other crushing agents.
特許出願人 電気化学工業株式会社 (10)Patent applicant: Denki Kagaku Kogyo Co., Ltd. (10)
Claims (1)
物50〜95重量%と水硬性物質50〜5重量%からな
る主材100重量部に対し、セメント減水剤0.5〜3
重量部を含有させてなる脆性物体の破砕剤。0.5 to 3 parts by weight of a cement water reducing agent to 100 parts by weight of the main material consisting of 50 to 95% by weight of surface carbonates and 50 to 5% by weight of hydraulic substances of soft calcined lime powder with a crystal size of less than 10μ.
A crushing agent for brittle objects containing part by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57037653A JPS58154779A (en) | 1982-03-10 | 1982-03-10 | Breaking agent for brittle substance |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57037653A JPS58154779A (en) | 1982-03-10 | 1982-03-10 | Breaking agent for brittle substance |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS58154779A true JPS58154779A (en) | 1983-09-14 |
Family
ID=12503600
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57037653A Pending JPS58154779A (en) | 1982-03-10 | 1982-03-10 | Breaking agent for brittle substance |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58154779A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60195270A (en) * | 1984-03-19 | 1985-10-03 | 電気化学工業株式会社 | Destruction of fragile matter |
WO2010143506A1 (en) | 2009-06-12 | 2010-12-16 | 電気化学工業株式会社 | Expansive admixture and method for producing same |
-
1982
- 1982-03-10 JP JP57037653A patent/JPS58154779A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60195270A (en) * | 1984-03-19 | 1985-10-03 | 電気化学工業株式会社 | Destruction of fragile matter |
WO2010143506A1 (en) | 2009-06-12 | 2010-12-16 | 電気化学工業株式会社 | Expansive admixture and method for producing same |
KR20120036833A (en) | 2009-06-12 | 2012-04-18 | 덴끼 가가꾸 고교 가부시키가이샤 | Expansive admixture and method for producing same |
JPWO2010143506A1 (en) * | 2009-06-12 | 2012-11-22 | 電気化学工業株式会社 | Expandable material and method for producing the same |
US8663383B2 (en) | 2009-06-12 | 2014-03-04 | Denki Kagaku Kogyo Kabushiki Kaisha | Expansive material and its preparation process |
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