JPS63600B2 - - Google Patents

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Publication number
JPS63600B2
JPS63600B2 JP9328580A JP9328580A JPS63600B2 JP S63600 B2 JPS63600 B2 JP S63600B2 JP 9328580 A JP9328580 A JP 9328580A JP 9328580 A JP9328580 A JP 9328580A JP S63600 B2 JPS63600 B2 JP S63600B2
Authority
JP
Japan
Prior art keywords
acid
synthetic resin
fixing
agent
cartridge
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
Application number
JP9328580A
Other languages
Japanese (ja)
Other versions
JPS5719497A (en
Inventor
Tadao Maeda
Tsugio Shimojo
Katsumi Utsuki
Takao Saito
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
NOF Corp
Original Assignee
Nippon Oil and Fats Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nippon Oil and Fats Co Ltd filed Critical Nippon Oil and Fats Co Ltd
Priority to JP9328580A priority Critical patent/JPS5719497A/en
Publication of JPS5719497A publication Critical patent/JPS5719497A/en
Publication of JPS63600B2 publication Critical patent/JPS63600B2/ja
Granted legal-status Critical Current

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  • Rock Bolts (AREA)

Description

【発明の詳細な説明】 本発明は岩盤等に穿孔した孔内にロツクボルト
等を固着し岩盤等を補強するためのロツクボルト
固着用カートリツジに関し、特に鉱山、発電所、
道路、鉄道等の各種トンネルにおいて、軟弱な岩
盤を強化するために有効な膨張性ロツクボルト固
着用カートリツジに関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a lock bolt fixing cartridge for fixing a lock bolt or the like in a hole drilled in a rock or the like to reinforce the rock or the like, and is particularly applicable to mines, power plants, etc.
This invention relates to a cartridge for fixing expandable lock bolts that is effective for strengthening soft rock in various tunnels such as roads and railways.

従来、トンネル工事等において、軟弱な岩盤に
穿孔し、その孔内にロツクボルト固着用カートリ
ツジを装填し、ついでロツクボルトを回転しなが
ら装着し、そのロツクボルト固着用カートリツジ
内の固着剤を撹拌して硬化させ、岩盤の孔内にロ
ツクボルトを固着させる方法が知られている。
Conventionally, in tunnel construction, etc., a hole is drilled into soft rock, a lock bolt fixing cartridge is loaded into the hole, the lock bolt is then installed while rotating, and the fixing agent in the lock bolt fixing cartridge is stirred and hardened. A method is known in which a rock bolt is fixed in a hole in a rock.

しかし軟弱な地盤では、内部の孔径が大きくな
り過ぎたり、亀裂があつたりして固着剤を孔内に
十分に満たすことができないので、孔内に固着剤
を十分に満し、さらに固着強度を上げるために、
発泡性のポリウレタン樹脂を用いた固着剤が提案
された(特開昭53−100607号)。しかし、このポ
リウレタン樹脂は常に一定の発泡倍率を得ること
が困難であつた。すなわち、この固着剤の反応は
ポリオールと架橋剤であるイソシアネートとの硬
化反応およびイソシアネートと水との公知の発泡
反応よりなるが、この発泡反応は岩盤の孔内にほ
とんどの場合水分があるために、この水分量によ
り影響を受け、さらに岩盤の孔内の温度にも影響
されるために発泡倍率を調節する事が困難であつ
た。また発泡が硬化反応に比較して速すぎれば、
ロツクボルト用固着剤は岩盤の孔内から流れ出し
その結果十分な固着強度を得ることができず、逆
に硬化反応の方が速いと固着剤は早く硬化して孔
内に満されないで終り、十分な固着強度を得るこ
とはできなかつた。
However, in soft ground, the internal hole diameter becomes too large or there are cracks, making it impossible to fully fill the hole with adhesive. In order to raise
A fixing agent using foamable polyurethane resin was proposed (Japanese Patent Application Laid-open No. 100607/1983). However, it has been difficult to always obtain a constant expansion ratio with this polyurethane resin. That is, the reaction of this fixing agent consists of a curing reaction between polyol and isocyanate, which is a crosslinking agent, and a well-known foaming reaction between isocyanate and water. It has been difficult to adjust the foaming ratio because it is affected by this water content and also by the temperature inside the hole in the rock. Also, if the foaming is too fast compared to the curing reaction,
The fixing agent for rock bolts flows out of the holes in the rock, and as a result, sufficient bonding strength cannot be obtained.On the other hand, if the curing reaction is faster, the fixing agent hardens quickly and ends up not filling the holes, resulting in sufficient bonding strength. It was not possible to obtain sufficient adhesion strength.

そこで既に本発明者らは不飽和ポリエステル樹
脂に有機酸または無機酸などの酸、硬化促進剤お
よび以上の酸に対して不活性な充填剤、さらに水
を加えて袋内に収容し、有機過酸化物からなる硬
化剤と炭酸塩または重炭酸塩からなる酸分解性発
泡剤とを収容した容器を袋中に入れた膨張性ロツ
クボルト固着用カートリツジを発明した。このも
のの使用に当つては孔内で容器を破壊して、全部
の薬剤を混合することにより、酸と酸分解性発泡
剤とを反応させ炭酸ガスを発生させて不飽和ポリ
エステル樹脂を発泡膨張させたものであつた。
Therefore, the present inventors have already added an acid such as an organic acid or an inorganic acid, a curing accelerator, a filler inert to the above acids, and water to an unsaturated polyester resin, and placed the mixture in a bag. We have invented a cartridge for fixing an inflatable lock bolt in which a container containing a curing agent consisting of an oxide and an acid-decomposable blowing agent consisting of a carbonate or bicarbonate is placed in a bag. When using this product, the container is broken inside the hole and all the chemicals are mixed together. The acid and acid-decomposable foaming agent are reacted to generate carbon dioxide gas, which causes the unsaturated polyester resin to foam and expand. It was warm.

このような膨張性ロツクボルト固着用カートリ
ツジにおいては酸または酸分解性発泡剤の一方が
反応によつて消費されれば発泡反応は終了し、そ
れ以上には発泡膨張しない利点があつた。しかし
不飽和ポリエステル樹脂とともに酸および水を配
置した場合、混合後1ケ月以内程度の比較的短時
間の保管後の使用時には理論量の発泡倍率を得る
ことができるが、長期保管すると、酸と接触する
ことによる不飽和ポリエステル樹脂の劣化、酸の
外部への放散等のために発泡倍率の低下を起すこ
とがある。
In such an expandable lock bolt fixing cartridge, the foaming reaction ends when either the acid or the acid-decomposable foaming agent is consumed by the reaction, and there is an advantage that no further foaming and expansion occurs. However, when acid and water are placed together with unsaturated polyester resin, it is possible to obtain the theoretical foaming ratio when used after being stored for a relatively short period of time, about one month after mixing, but when stored for a long period of time, it comes into contact with acid. This may cause deterioration of the unsaturated polyester resin, diffusion of acid to the outside, etc., resulting in a decrease in expansion ratio.

本発明者らはこのような欠点を解決し、かつ用
いた酸が施工者にかかるような不測の事態をさけ
る方法を検討した結果、酸および水には、増粘剤
を加えて熱硬化性合成樹脂とよく混合するような
粘度に増粘し、増粘された酸を熱硬化性合成樹脂
または酸分解性発泡剤などと隔離するため破壊可
能な容器に収納して熱硬化性合成樹脂等を収容す
る袋内に配置することにより長期間の保存に耐
え、適当な膨張性を有し、しかも酸が逸散しない
膨張性ロツクボルト固着用カートリツジを得た。
The inventors of the present invention have investigated ways to solve these drawbacks and avoid unexpected situations where the acid used may come into contact with the installer. As a result, they added a thickener to the acid and water to make it thermosetting. The thermosetting synthetic resin, etc. is thickened to a viscosity that mixes well with the synthetic resin, and is stored in a breakable container to separate the thickened acid from the thermosetting synthetic resin or acid-decomposable foaming agent. A cartridge for fixing an expandable lock bolt that can withstand long-term storage, has appropriate expandability, and prevents acid from escaping was obtained.

すなわち、本発明の膨張性ロツクボルト固着用
カートリツジは、熱硬化性合成樹脂と酸分解性発
泡剤と必要により加えられる前記熱硬化性合成樹
脂の硬化促進剤とからなる主剤を充填した軟質合
成樹脂袋中に、前記熱硬化性合成樹脂の硬化剤を
充填した破壊可能な容器および増粘剤と混合する
ことにより20℃における粘度を0.1〜4000ポイズ
とした増粘された酸を充填した他の破壊可能な容
器を収容してなる膨張性ロツクボルト固着用カー
トリツジである。
That is, the expandable lock bolt fixing cartridge of the present invention is a soft synthetic resin bag filled with a base material consisting of a thermosetting synthetic resin, an acid-decomposable foaming agent, and a curing accelerator for the thermosetting synthetic resin added as necessary. A breakable container filled with a curing agent for the thermosetting synthetic resin and another breakable container filled with a thickened acid having a viscosity of 0.1 to 4000 poise at 20°C by mixing with a thickener. This is a cartridge for fixing an inflatable lock bolt, which accommodates a container that can be used.

この膨張性ロツクボルト固着用カートリツジ中
には、熱硬化性合成樹脂と酸分解性発泡剤と必要
により加えられる硬化促進剤とからなる主剤と、
熱硬化性合成樹脂の硬化剤と、増粘剤にて増粘さ
れた酸との三つの構成剤を互に隔離して袋中に収
納するもので、これらの構成剤を総称して固着剤
という。
This expansible lock bolt fixing cartridge contains a main agent consisting of a thermosetting synthetic resin, an acid-decomposable foaming agent, and a curing accelerator added as necessary;
Three components, a curing agent for thermosetting synthetic resin and an acid thickened with a thickener, are separated from each other and stored in a bag, and these components are collectively called a fixing agent. That's what it means.

本発明に用いることのできる熱硬化性合成樹脂
は、たとえば不飽和ポリエステル樹脂、エポキシ
樹脂等で、硬化前の合成樹脂に硬化剤を加えて硬
化するものである。不飽和ポリエステル樹脂を用
いる場合には、無水マレイン酸、フマル酸等の
α,β―不飽和二塩基酸またはこのα,β―不飽
和二塩基酸の一部を無水フタル酸、イソフタル
酸、テレフタル酸等の飽和二塩基酸成分で置換し
たものと、エチレングリコール、ジプロピレング
リコール、水素化ビスフエノールA等のグリコー
ル類とをモル比約1:1で重縮合して得られる不
飽和ポリエステルをスチレン、ビニルトルエン、
クロロスチレン、ジビニルベンゼン、ジアリルフ
タレート、アクリル酸エステル、メタアクリル酸
エステル類等の架橋用不飽和単量体に溶解し、ハ
イドロキノン等の重合禁止剤を加えて硬化前の不
飽和ポリエステル樹脂を製造する。
Thermosetting synthetic resins that can be used in the present invention include, for example, unsaturated polyester resins and epoxy resins, which are cured by adding a curing agent to the synthetic resin before curing. When using an unsaturated polyester resin, α,β-unsaturated dibasic acids such as maleic anhydride and fumaric acid, or a part of this α,β-unsaturated dibasic acid, may be substituted with phthalic anhydride, isophthalic acid, or terephthalic acid. Styrene is an unsaturated polyester obtained by polycondensing a substance substituted with a saturated dibasic acid component such as an acid and a glycol such as ethylene glycol, dipropylene glycol, or hydrogenated bisphenol A at a molar ratio of about 1:1. , vinyltoluene,
It is dissolved in unsaturated crosslinking monomers such as chlorostyrene, divinylbenzene, diallyl phthalate, acrylic esters, and methacrylic esters, and a polymerization inhibitor such as hydroquinone is added to produce an unsaturated polyester resin before curing. .

不飽和ポリエステル樹脂の硬化剤としては有機
過酸化物が用いられる。それぞれの熱硬化性合成
樹脂に対して適切な有機過酸化物が用いられ、た
とえば不飽和ポリエステル樹脂に対しては、ベン
ゾイルパーオキサイド、シクロヘキサノンパーオ
キサイド、ターシヤリプチルハイドロパーオキサ
イド等であり、特に取り扱い易さからベンゾイル
パーオキサイドが好ましい。またこれらの有機過
酸化物はタルク、クレイ、炭酸カルシウム、硫酸
カルシウム等の無機質の稀釈剤またはパルプ粉
末、ジアリルフタレート粉等の有機化合物の稀釈
剤で稀釈して使用することが分散性および安全性
の面からも望ましい。
Organic peroxides are used as curing agents for unsaturated polyester resins. An appropriate organic peroxide is used for each thermosetting synthetic resin; for example, for unsaturated polyester resins, benzoyl peroxide, cyclohexanone peroxide, tertiarybutyl hydroperoxide, etc. Benzoyl peroxide is preferred because of its ease of use. In addition, these organic peroxides should be diluted with an inorganic diluent such as talc, clay, calcium carbonate, or calcium sulfate, or an organic compound diluent such as pulp powder or diallyl phthalate powder to improve dispersibility and safety. It is also desirable from the viewpoint of

不飽和ポリエステル樹脂の硬化促進剤として
は、ジメチルアニリン、ジエチルアニリン等の第
三級アミン類があり、その使用量は前記不飽和ポ
リエステル樹脂100重量部に対して0.01〜5重量
部、好ましくは0.05〜1.0重量部である。5重量
部より多くなると貯蔵安定性が悪くなり、0.01重
量部より少なくなると不飽和ポリエステル樹脂の
硬化速度が遅くなつて好ましくない。
Examples of curing accelerators for unsaturated polyester resins include tertiary amines such as dimethylaniline and diethylaniline, and the amount used is 0.01 to 5 parts by weight, preferably 0.05 parts by weight, based on 100 parts by weight of the unsaturated polyester resin. ~1.0 parts by weight. If the amount is more than 5 parts by weight, storage stability will deteriorate, and if it is less than 0.01 part by weight, the curing speed of the unsaturated polyester resin will be undesirably slow.

本発明に用いることのできる酸分解性発泡剤と
しては、たとえばカリウム、ナトリウム等のアル
カリ金属の炭酸塩または重炭酸塩、カルシウム等
のアルカリ土類金属の炭酸塩または重炭酸塩、炭
酸アンモニウム、重炭酸アンモニウム等がある。
Examples of acid-decomposable blowing agents that can be used in the present invention include carbonates or bicarbonates of alkali metals such as potassium and sodium; carbonates or bicarbonates of alkaline earth metals such as calcium; ammonium carbonate; Examples include ammonium carbonate.

本発明に用いることのできる酸としては蟻酸、
酢酸、プロピオン酸、乳酸等の有機酸または稀塩
酸、稀硫酸、稀硝酸等の無機酸であり、その使用
量はたとえば不飽和ポリエステル樹脂100重量部
に対して純品換算で1〜10重量部である。
Acids that can be used in the present invention include formic acid,
These are organic acids such as acetic acid, propionic acid, and lactic acid, or inorganic acids such as dilute hydrochloric acid, dilute sulfuric acid, and dilute nitric acid, and the amount used is, for example, 1 to 10 parts by weight in pure terms per 100 parts by weight of unsaturated polyester resin. It is.

酸の増粘剤としては、有機質の増粘剤として水
に可溶性の高分子、たとえばポリビニルアルコー
ル、カルボキシメチルセルロース、メチルセルロ
ース、ヒドロキシエチルセルロース、ポリアクリ
ルアミド等の水溶液を使用することができる。ま
たデキストリン、でんぷん、ゼラチン等も使用す
ることができる。また無水珪酸、ベントナイト等
の無機質の増粘剤も単独あるいは有機質の増粘剤
と組合わせて使用することができる。さらに粘度
を調節するために酸に対して安定な充填剤、たと
えば硫酸バリウム、酸化アルミニウム、硫酸カル
シウム等も添加することができる。
As the acid thickener, an aqueous solution of a water-soluble polymer such as polyvinyl alcohol, carboxymethyl cellulose, methyl cellulose, hydroxyethyl cellulose, polyacrylamide, etc. can be used as an organic thickener. Dextrin, starch, gelatin, etc. can also be used. Inorganic thickeners such as silicic anhydride and bentonite can also be used alone or in combination with organic thickeners. Furthermore, acid-stable fillers such as barium sulfate, aluminum oxide, calcium sulfate, etc. can also be added to adjust the viscosity.

酸の粘度は主として使用する熱硬化性合成樹脂
を含む主剤の粘度により決定される。熱硬化性合
成樹脂を含む主剤の粘度が低い場合、酸の粘度は
当然それに合わせた低い粘度のものが望ましい。
また逆に熱硬化性合成樹脂を含む主剤の粘度が高
い場合酸の粘度は高い方が望ましい。しかし本発
明の粘度範囲で適宜粘度を変えて使用することが
でき、組合わせの使用制限を受けるものではな
い。
The viscosity of the acid is mainly determined by the viscosity of the base material containing the thermosetting synthetic resin used. When the viscosity of the base resin containing the thermosetting synthetic resin is low, it is naturally desirable that the viscosity of the acid is low enough to match the viscosity of the base resin.
Conversely, when the viscosity of the base resin containing a thermosetting synthetic resin is high, it is desirable that the viscosity of the acid be high. However, the viscosity can be changed as appropriate within the viscosity range of the present invention, and there are no restrictions on the combinations used.

既に述べた酸分解性発泡剤としての炭酸塩、重
炭酸塩は熱硬化性合成樹脂と混合して充填剤とし
ても用いられる。すなわち使用する酸に対して反
応に必要な量の10倍ないし100倍の炭酸塩または
重炭酸塩を加えると、一部は酸と反応して熱硬化
性合成樹脂の膨張に利用され、残りは熱硬化性合
成樹脂の充填剤として利用できる。酸に対して過
剰な酸分解性発泡剤を使用すれば、同量の酸に対
して当量の酸分解発泡剤を用いた場合より熱硬化
性合成樹脂の発泡膨張時間は短縮される。この事
は熱硬化性合成樹脂が硬化する前に酸が完全に消
費され、熱硬化性合成樹脂の発泡膨張性を終了さ
せ、常に一定の発泡膨張を得るので非常に有利で
ある。
Carbonates and bicarbonates as the acid-decomposable blowing agents mentioned above can also be used as fillers by being mixed with thermosetting synthetic resins. In other words, when carbonate or bicarbonate is added in an amount of 10 to 100 times the amount required for the reaction to the acid used, a portion will react with the acid and be used to expand the thermosetting synthetic resin, and the rest will be used to expand the thermosetting synthetic resin. It can be used as a filler for thermosetting synthetic resins. If an excess of acid-decomposable blowing agent is used relative to the acid, the foaming expansion time of the thermosetting synthetic resin will be shorter than when using an equivalent amount of acid-decomposable blowing agent to the same amount of acid. This is very advantageous, since the acid is completely consumed before the thermosetting synthetic resin hardens, ending the foaming expansion properties of the thermosetting synthetic resin and always obtaining a constant foaming expansion.

以上のように添加する物質の他に、酸と反応し
ない他の充填剤たとえば珪砂粉、ガラス粉、タル
ク、クレー、硫酸バリウムを前述の酸分解性発泡
剤と混合して利用できる。また熱硬化性合成樹脂
の安定剤、整泡剤を加えることもできる。
In addition to the substances added above, other fillers that do not react with acids, such as silica sand powder, glass powder, talc, clay, and barium sulfate, can be used by mixing them with the acid-decomposable blowing agent. In addition, a stabilizer for thermosetting synthetic resin and a foam stabilizer can also be added.

次に容器について述べると、熱硬化性合成樹脂
と酸分解性発泡剤と必要により加えられた硬化促
進剤とを充填する合成樹脂製薄膜袋としてはたと
えばポリエチレン、ポリアミド等の合成樹脂製薄
膜袋が用いられる。熱硬化性合成樹脂の硬化剤を
充填した破壊可能な容器または増粘剤を混合する
ことにより増粘された酸を充填した他の破壊可能
な容器の材料としてはガラス管、セラミツク管ま
たは合成樹脂製薄膜袋等が用いられる。
Next, regarding containers, thin film bags made of synthetic resin such as polyethylene, polyamide, etc. are used as thin film bags made of synthetic resin to fill the thermosetting synthetic resin, acid-decomposable foaming agent, and curing accelerator added if necessary. used. Materials for breakable containers filled with curing agents of thermosetting synthetic resins or other breakable containers filled with acids thickened by mixing with thickeners include glass tubes, ceramic tubes or synthetic resins. A thin film bag or the like is used.

次に実施例および比較例について述べる。 Next, examples and comparative examples will be described.

実施例 1 〔固着剤の各構成剤の調製〕 無水マレイン酸490.5g、無水フタル酸740.5
g、プロピレングリコール837gを150〜160℃で
反応させて得られた不飽和ポリエステル1295gに
スチレン555gを加え、さらにハイドロキノン0.2
gを添加して硬化前の不飽和ポリエステル樹脂
(酸価30)1850gを得た。この硬化前の不飽和ポ
リエステル樹脂のうち370gをとりジメチルアニ
リン0.74g、タルク100g、炭酸カルシウム100
g、シリコン系整泡剤(信越化学工業株式会社製
F305)1.9gを加え品川式撹拌機で30分間撹拌し
て均一に混合することにより主剤560gを得た。
B型粘度計で測定したこの主剤の粘度は20℃で20
ポイズであつた。
Example 1 [Preparation of each component of the fixing agent] Maleic anhydride 490.5g, phthalic anhydride 740.5g
555 g of styrene was added to 1295 g of unsaturated polyester obtained by reacting 837 g of propylene glycol at 150 to 160°C, and 0.2 g of hydroquinone was added.
g was added to obtain 1850 g of unsaturated polyester resin (acid value: 30) before curing. Take 370g of this unsaturated polyester resin before curing, add 0.74g of dimethylaniline, 100g of talc, and 100g of calcium carbonate.
g. Silicone foam stabilizer (manufactured by Shin-Etsu Chemical Co., Ltd.)
F305) 1.9g was added and stirred for 30 minutes using a Shinagawa stirrer to mix uniformly, yielding 560g of the main ingredient.
The viscosity of this base agent measured with a B-type viscometer is 20 at 20°C.
It was poise.

次にベンゾイルパーオキサイド7.1gと炭酸カ
ルシウム16.9gを混合し硬化剤24gを得た。
Next, 7.1 g of benzoyl peroxide and 16.9 g of calcium carbonate were mixed to obtain 24 g of a hardening agent.

次にメチルセルロース(400CP)1gを水16g
に溶解し、酢酸4gを加え、よく混合溶解させ、
さらに硫酸バリウム20gを加えた。この増粘され
た後の粘度をB型粘度計で測定すると、20℃で20
ポイズであつた。
Next, add 1g of methylcellulose (400CP) to 16g of water.
Add 4g of acetic acid, mix well and dissolve.
Furthermore, 20 g of barium sulfate was added. When the viscosity after this thickening was measured using a B-type viscometer, it was found to be 20% at 20°C.
It was poise.

〔膨張性ロツクボルト固着用カートリツジの調製〕[Preparation of cartridge for fixing expandable lock bolt]

前述のように製造した主剤を内径32mm、長さ
500mmのポリアミド製の袋内に装填し、硬化剤を
内径10mm、長さ450mmのガラス管に封入し、メチ
ルセルロースで増粘した酢酸を内径8mm、長さ
450mmのガラス管に封入した。この2本のガラス
管を主剤を充填したポリアミド製袋中の主剤の中
に挿入し、袋の口を閉塞してカートリツジを調製
した。
The main material produced as described above was used to
Loaded into a 500 mm polyamide bag, the curing agent was sealed in a glass tube with an inner diameter of 10 mm and a length of 450 mm, and acetic acid thickened with methylcellulose was placed in a glass tube with an inner diameter of 8 mm and a length of 450 mm.
It was sealed in a 450mm glass tube. These two glass tubes were inserted into the base agent in a polyamide bag filled with the base agent, and the mouth of the bag was closed to prepare a cartridge.

〔装着および引抜試験I〕 前記のカートリツジ2本を圧縮強度120Kg/cm2
の乾燥した砂岩の上向孔内(孔径42mm、孔長2
m)に装填し、外径25mm長さ2.2mの異形棒鋼
(D―25、以下同様)を回転させながら打込んだ。
打込3分後固着剤は口元から約20cmのところまで
膨張してきた。24時間後センターホール型油圧ジ
ヤツキーでロツクボルトを引抜いて、その時の引
抜荷重を測定した。測定の結果は21トンでボルト
が破断した。膨張倍率は2倍であつた。
[Installation and pull-out test I] The above two cartridges were tested at a compressive strength of 120Kg/cm 2
In a dry sandstone upward hole (hole diameter 42 mm, hole length 2
m), and a deformed steel bar (D-25, hereinafter the same) with an outer diameter of 25 mm and a length of 2.2 m was driven while rotating.
After 3 minutes of application, the adhesive expanded to about 20 cm from the mouth. After 24 hours, the lock bolt was pulled out using a center hole type hydraulic jack, and the pullout load at that time was measured. The measurement results showed that the bolt broke at 21 tons. The expansion ratio was 2 times.

〔装着および引抜試験〕 前記のカートリツジ2本を圧縮強度120Kg/cm2
の砂岩に穿孔した上向孔(孔径42mm、孔長2m)
に装填し、外径25mm、長さ2.2mの異形棒鋼を天
井に垂直に打込んだ。打込してから3分経過後固
着剤は口元から20cmのところまで膨張してきた。
24時間後にセンターホール型油圧ジヤツキーでロ
ツクボルトを引抜いて限界の引抜荷重を測定し
た。22トンの引抜荷重でボルトが破断した。膨張
倍率は2倍であつた。
[Installation and pull-out test] Two of the above cartridges were tested with a compressive strength of 120Kg/cm 2
Upward hole drilled in sandstone (hole diameter 42mm, hole length 2m)
A deformed steel bar with an outer diameter of 25 mm and a length of 2.2 m was driven vertically into the ceiling. Three minutes after the injection, the adhesive expanded to a distance of 20 cm from the mouth.
After 24 hours, the lock bolt was pulled out using a center hole type hydraulic jack and the maximum pulling load was measured. The bolt broke under a pullout load of 22 tons. The expansion ratio was 2 times.

〔装着および引抜試験〕 前記のカートリツジを製造後室温で6ケ月放置
した後装着および引抜試験と同様の試験を行な
つた。膨張率を観察したところ、固着剤は口元か
ら23cmのところまで膨張してきた。またその時の
引抜試験の引抜荷重が22トンでボルトが破断し
た。
[Mounting and pull-out test] The above cartridge was left at room temperature for 6 months after manufacture, and then a test similar to the mounting and pull-out test was conducted. When the expansion rate was observed, the adhesive expanded to a distance of 23 cm from the mouth. Also, the bolt broke at a pullout load of 22 tons during the pullout test.

実施例 2 〔固着剤の各構成剤の調製〕 実施例1で得られた硬化前の不飽和ポリエステ
ル樹脂のうち350gをとりこれにジメチルアニリ
ン0.7g、タルク150g、炭酸カルシウム150g、
シリコン系整泡剤1.8gを加え、品川式撹拌機で
30分間撹拌し均一に混合して主剤600gを得た。
B型粘度計で測定した主剤の粘度は20℃で2500ポ
イズであつた。
Example 2 [Preparation of each component of the fixing agent] Take 350 g of the uncured unsaturated polyester resin obtained in Example 1 and add 0.7 g of dimethylaniline, 150 g of talc, 150 g of calcium carbonate,
Add 1.8g of silicone foam stabilizer and mix using a Shinagawa stirrer.
The mixture was stirred for 30 minutes and mixed uniformly to obtain 600 g of the main ingredient.
The viscosity of the base agent measured with a B-type viscometer was 2500 poise at 20°C.

またベンゾイルパーオキサイド7.1gと炭酸カ
ルシウム16.9gを混合して硬化剤24gを得た。
Further, 7.1 g of benzoyl peroxide and 16.9 g of calcium carbonate were mixed to obtain 24 g of a hardening agent.

さらにベントナイト3gと硫酸バリウム17gと
に水16gおよび塩酸2gを加えて〓つて得られた
増粘された酸の粘度は20℃で2000ポイズであつ
た。
Further, 16 g of water and 2 g of hydrochloric acid were added to 3 g of bentonite and 17 g of barium sulfate, and the resulting thickened acid had a viscosity of 2000 poise at 20°C.

〔膨張性ロツクボルト固着用カートリツジの調製〕[Preparation of cartridge for fixing expandable lock bolt]

実施例1と同様の方法で膨張性ロツクボルト固
着用カートリツジを調製した。
A cartridge for fixing an inflatable lock bolt was prepared in the same manner as in Example 1.

〔装着および引抜試験〕 前述のカートリツジ3本を圧縮強度300Kg/cm2
の頁岩で湧水のある上向孔(孔径42mm、孔長2
m)に装填し、外径25mm、長さ2.2mの異形棒鋼
を回転しながら打込んだ。打込み後約5分で固着
剤は膨張して孔の口元まで到達した。
[Installation and pull-out test] The three cartridges mentioned above had a compressive strength of 300Kg/cm 2
Upward hole with spring water in shale (hole diameter 42 mm, hole length 2
m), and a deformed steel bar with an outer diameter of 25 mm and a length of 2.2 m was driven while rotating. Approximately 5 minutes after implantation, the adhesive expanded and reached the mouth of the hole.

打込み後24時間経過後、センターホール型油圧
ジヤツキーでロツクボルトを引抜いた所、引抜荷
重は23トンでボルトが破断した。膨張倍率は1.5
倍であつた。
24 hours after driving, the lock bolt was pulled out using a center hole type hydraulic jack, and the bolt broke at a pullout load of 23 tons. Expansion magnification is 1.5
It was twice as hot.

比較例 1 〔膨張性ロツクボルト固着用カートリツジの調
製〕 主剤および硬化剤は実施例1と同じ方法にて調
製し、主剤は実施例1と同様なポリアミド製の袋
内に装填し、硬化剤は実施例1と同様なガラス管
に封入した。
Comparative Example 1 [Preparation of a cartridge for fixing an inflatable lock bolt] The base resin and curing agent were prepared in the same manner as in Example 1. The base resin was loaded into the same polyamide bag as in Example 1, and the curing agent was prepared in the same manner as in Example 1. It was sealed in a glass tube similar to Example 1.

次に酢酸4gに水16gを加えた溶液を内径8
mm、長さ45cmのガラス管内に封入した。
Next, add a solution of 4 g of acetic acid and 16 g of water to a
It was sealed in a glass tube with a diameter of 45 cm and a length of 45 cm.

主剤を充填したポリアミド製袋内に前述の2本
のガラス管を封入し、膨張性ロツクボルト固着用
カートリツジを製造した。
The two glass tubes described above were sealed in a polyamide bag filled with the base material to produce a cartridge for fixing an expandable lock bolt.

〔装着および引抜試験〕 圧縮強度120Kg/cm2の砂岩に穿孔した上向孔
(孔径42mm、長さ2m)に前述のカートリツジ2
本を挿入し、異形棒鋼を打込んだ。24時間後観測
すると口元より90cm内部で固着剤の膨張は止つて
いた。発泡倍率は1.2倍であり、引抜試験の結果
引抜荷重19トンでボルトが抜けた。
[Installation and pull-out test] The above-mentioned cartridge 2 was inserted into an upward hole (hole diameter 42 mm, length 2 m) drilled in sandstone with a compressive strength of 120 kg/cm 2.
A book was inserted and a deformed steel bar was driven into it. When observed after 24 hours, the expansion of the adhesive had stopped 90 cm from the mouth. The foaming ratio was 1.2 times, and as a result of the pull-out test, the bolt came out at a pull-out load of 19 tons.

比較例 2 〔膨張式ロツクボルト固着用カートリツジの調
製〕 主剤および硬化剤は実施例2と同じ方法で調製
し、主剤は実施例1と同様なポリアミド製の袋内
に装填し、硬化剤は実施例1と同様なガラス管に
封入した。
Comparative Example 2 [Preparation of a cartridge for fixing an inflatable lock bolt] The base material and hardening agent were prepared in the same manner as in Example 2. The base material was loaded into the same polyamide bag as in Example 1, and the hardening agent was prepared in the same manner as in Example 1. It was sealed in a glass tube similar to 1.

次に塩酸2gに水16gを加えた溶液を内径8
mm、長さ45cmのガラス管内に封入した。
Next, add a solution of 2 g of hydrochloric acid and 16 g of water to a
It was sealed in a glass tube with a diameter of 45 cm and a length of 45 cm.

次に主剤を充填したポリアミド製袋内に前述の
2本のガラス管を封入し、膨張性ロツクボルト固
着用カートリツジを製造した。
Next, the two glass tubes described above were sealed in a polyamide bag filled with the base material to produce a cartridge for fixing an expandable lock bolt.

〔装着および引抜試験〕 圧縮強度120Kg/cm2の砂岩の天井に穿孔した上
向孔(孔径42mm、長さ2m)に前述のカートリツ
ジ2本を挿入し、異形棒鋼を打込んだ。打込後24
時間経過した後に観測すると発泡倍率は1.1倍で
固着剤は孔の口元より100cm奥で止まつてしまい、
かつ異形棒鋼の打込時に天井より酸性の水がたれ
てきた。引抜荷重が20トンでボルトが抜けた。
[Installation and pull-out test] Two of the aforementioned cartridges were inserted into an upward hole (hole diameter: 42 mm, length: 2 m) drilled in a sandstone ceiling with a compressive strength of 120 Kg/cm 2 , and a deformed steel bar was driven into it. 24 after driving
When observed after some time had elapsed, the foaming magnification was 1.1 times, and the adhesive stopped 100cm deep from the mouth of the hole.
Additionally, acidic water was dripping from the ceiling during the driving of deformed steel bars. The bolt came off when the pulling load was 20 tons.

以上に述べたように本発明の膨張性ロツクボル
ト固着用カートリツジは適宜な発泡倍率を有する
とともに引抜に耐える引抜荷重も高く、十分膨張
性ロツクボルト固着用カートリツジとしての効果
を示すものである。また、酸を直接容器に封入す
ると異形棒鋼の打込後酸滴が酸分解性発泡剤と反
応しないでもれ出すものがでてきて十分の膨張倍
率が期待できないのに対して、本発明の膨張性ロ
ツクボルト固着用カートリツジは増粘された酸を
用いているので酸がもれ出すことなく、十分な発
泡反応を行なうことができ、有効なものである。
As described above, the inflatable lock bolt fixing cartridge of the present invention has an appropriate expansion ratio and a high pullout load to withstand pulling out, and is sufficiently effective as an expandable lock bolt fixing cartridge. In addition, if acid is directly sealed in a container, some acid droplets will leak out after the deformed steel bar is driven without reacting with the acid-decomposable foaming agent, making it impossible to expect a sufficient expansion ratio. The cartridge for fixing the adhesive lock bolt is effective because it uses a thickened acid, so that a sufficient foaming reaction can be carried out without acid leakage.

Claims (1)

【特許請求の範囲】[Claims] 1 熱硬化性合成樹脂と酸分解性発泡剤と必要に
より加えられる前記熱硬化性合成樹脂の硬化促進
剤とからなる主剤を充填した合成樹脂製薄膜袋中
に、前記熱硬化性合成樹脂の硬化剤を充填した破
壊可能な容器と、酸と増粘剤とを混合することに
より20℃における粘度を0.1〜4000ポイズとした
増粘された酸を充填した他の破壊可能な容器とを
収納してなる膨張性ロツクボルト固着用カートリ
ツジ。
1. Curing of the thermosetting synthetic resin is carried out in a synthetic resin thin film bag filled with a main ingredient consisting of a thermosetting synthetic resin, an acid-decomposable blowing agent, and a curing accelerator for the thermosetting synthetic resin added as necessary. A breakable container filled with an acid and another breakable container filled with an acid whose viscosity at 20°C has been increased to 0.1 to 4000 poise by mixing the acid and a thickener are housed. Cartridge for fixing expandable lock bolts.
JP9328580A 1980-07-10 1980-07-10 Cartridge for fastening expansive rock bolt Granted JPS5719497A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9328580A JPS5719497A (en) 1980-07-10 1980-07-10 Cartridge for fastening expansive rock bolt

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9328580A JPS5719497A (en) 1980-07-10 1980-07-10 Cartridge for fastening expansive rock bolt

Publications (2)

Publication Number Publication Date
JPS5719497A JPS5719497A (en) 1982-02-01
JPS63600B2 true JPS63600B2 (en) 1988-01-07

Family

ID=14078136

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9328580A Granted JPS5719497A (en) 1980-07-10 1980-07-10 Cartridge for fastening expansive rock bolt

Country Status (1)

Country Link
JP (1) JPS5719497A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6028478A (en) * 1983-07-27 1985-02-13 Asahi Chem Ind Co Ltd Bolt-setting fixing agent with high corrosion resistance
JPS60173071A (en) * 1984-02-20 1985-09-06 Asahi Chem Ind Co Ltd Bolt fixing agent
JPS60188484A (en) * 1984-03-09 1985-09-25 Asahi Chem Ind Co Ltd Material for fixing corrosion-resistant bolt
JP6985055B2 (en) * 2017-08-02 2021-12-22 旭化成株式会社 Adhesive for building structures

Also Published As

Publication number Publication date
JPS5719497A (en) 1982-02-01

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