JPS588417B2 - Solidification method of gas phase-solid phase composite material - Google Patents
Solidification method of gas phase-solid phase composite materialInfo
- Publication number
- JPS588417B2 JPS588417B2 JP52137578A JP13757877A JPS588417B2 JP S588417 B2 JPS588417 B2 JP S588417B2 JP 52137578 A JP52137578 A JP 52137578A JP 13757877 A JP13757877 A JP 13757877A JP S588417 B2 JPS588417 B2 JP S588417B2
- Authority
- JP
- Japan
- Prior art keywords
- composite material
- gas phase
- solid
- solidifying
- cement
- 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
Landscapes
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Lining And Supports For Tunnels (AREA)
- Processing Of Solid Wastes (AREA)
Description
【発明の詳細な説明】
この発明は、気相一固相複合材料の固化方法に関し.特
に,殆んどが疎水性物質からなる気相一固相複合材科に
,予め陰イオン活性剤および微粒状シリカ溶液を浸透せ
しめでおいて.本来親水性物質であってこの気相一固相
複介材料には浸透ができないセメント.セメント一石こ
う系のペーストを浸透できるようにし、このペーストを
該複合材科に注入し.全体にペースト固化による硬さを
与えるものであり.換言すれば可撓部材を荷重K対する
支持力のある部材に改質する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for solidifying a gas phase-solid phase composite material. In particular, an anionic activator and a fine-grained silica solution are infiltrated in advance into a gas phase-solid phase composite material, which consists mostly of hydrophobic substances. Cement is originally a hydrophilic substance and cannot penetrate this gas-solid phase composite material. Allow the cement-gypsum paste to penetrate and inject this paste into the composite material. It gives hardness to the whole by solidifying the paste. In other words, the flexible member is modified into a member that has the ability to support the load K.
一般に.土木建設の現場.例えば.シールド工事におい
で,気相一固相複合材料をセグメント背面に接着してお
き.このセグメントをシールドテール内で組み立でる場
合,該複合材料は,セグメントとシールドテールプレー
トで圧縮され,泥水の浸入を防止する。in general. Civil engineering construction site. for example. During shield construction, a gas phase-solid phase composite material was glued to the back of the segment. When the segment is assembled within the shield tail, the composite material is compressed between the segment and the shield tail plate to prevent muddy water ingress.
シールド機械の前進にともないシールドテールから出た
前記複合材科は複元し地山の肌落ちを防ぐ。As the shield machine moves forward, the composite material that comes out of the shield tail is duplicated to prevent the surface of the ground from falling off.
この場合,複合材科は,なおその本来の弾性を有してお
り.地山を支えるに十分ではない。In this case, the composite material still has its original elasticity. Not enough to support the ground.
従って,地山のゆるみや沈下を生じることは免れない。Therefore, loosening and subsidence of the ground is inevitable.
また.このように使用した複合材科は,当然気泡が連続
しており,セグメントの接合部分からの漏水を完全に防
止することができない欠点を有しでいる。Also. The composite materials used in this manner naturally have continuous air bubbles and have the disadvantage that water leakage from the joints of the segments cannot be completely prevented.
この発明は,このように,始めは可撓性が要求され.後
にその可撓性が不要となり,むしろ剛性となることが要
求される気相一固相複合材料の固化方法を提供する。This invention thus initially required flexibility. The present invention provides a method for solidifying a gas phase-solid composite material, which does not need to be flexible, but rather needs to be rigid.
而して.この発明の目的は,親水性のセメント又はセメ
ント一石こう系ペーストを疎水性の気相一固相複合材料
の組織内に注入できる手段を提供するにあり.また,こ
の発明の目的は,気相一固相複合材科の弾性を利用した
後に.これを固化し耐荷重性のある充填材科を形成する
ことにあり,更に,この発明の目的は,土木工事に好適
な気相一固相複合材科一セメント系部材を提供するにあ
る。Then. The object of this invention is to provide a means for injecting hydrophilic cement or cement-gypsum paste into the structure of a hydrophobic gas-solid composite material. Moreover, the purpose of this invention is to utilize the elasticity of gas phase-solid phase composite materials. It is an object of the present invention to solidify this to form a load-bearing filler material.A further object of the present invention is to provide a gas-solid composite material-cement member suitable for civil engineering work.
即ち,この発明は,図示する実施例のように,弾性のあ
る気相一固相複合材料1に,予め,陰イオン活性剤およ
び微粒状シリカ溶液を浸透せしめ,然る後,セメントあ
るいはセメント一石こう系のペースト2を.前記気相一
固相複合材科の組織内に注入してから固化することを特
徴とする気相一固相複合材科の固化方法に係る。That is, in the present invention, as in the illustrated embodiment, an anionic activator and a particulate silica solution are infiltrated into an elastic gas-solid composite material 1 in advance, and then cement or a cement mixture is infiltrated. Gypsum-based paste 2. The present invention relates to a method for solidifying a vapor-solid composite material, characterized in that the vapor-solid composite material is injected into the tissue and then solidified.
この発明は,多くの疎水性物質からなる気相一固相複合
材科にこれと本質的に相異なる親水性物質からなるセメ
ント.セメント一石こう系材科を注入する技術であり.
そのため.該複合材科には.予め陰イオン活性剤および
微粒状シリカ溶液を浸透せしめてお匂
このような,陰イオン活性剤および微粒状シリ力溶液の
該複合材科の組織内への含浸け,その組織内の湿潤効果
を期待するものである。This invention combines a gas phase-solid phase composite material family consisting of many hydrophobic substances with a cement consisting of a hydrophilic substance that is essentially different from the gas phase-solid phase composite material family. It is a technology that injects cement and gypsum-based materials.
Therefore. In the composite materials department. By impregnating the anionic activator and the fine granular silica solution in advance into the tissue of the composite material, the anionic activator and the fine granular silica solution are impregnated into the tissue of the composite material, and the wetting effect in the tissue is enhanced. That's to be expected.
一般的に広く知られでいる気相一固相複合材科は,次の
如きものが挙げられでいる。The following are the generally well-known gas phase-solid phase composite materials.
これらの材料のうち,一つの固体としてまとまりさらに
弾性のある部材がこの発明の気相一固相複合材科として
好適である。Among these materials, members that are integrated as a single solid and have elasticity are suitable as the gas phase-solid phase composite material of the present invention.
この際使用する湿潤剤としての陰イオン系界面活性剤に
は,特に,洗浄効果より湿潤効果が期待できるスルフオ
琥珀酸エステル塩(ジアルキルスルフオサクシネート)
を使用するのがよい。As the anionic surfactant used as a wetting agent in this case, it is particularly preferable to use a sulfosuccinate salt (dialkyl sulfosuccinate), which is expected to have a wetting effect rather than a cleaning effect.
このフルフオ琥珀酸エステル塩は,分子の中心にスルフ
オ琥珀酸
の原子団を有し,この原子団のカルボン酸力ξ種種のア
ルコールによりエステル化されたエステル結合スルフオ
ネートで,マレイン酸エステルがその原科となる。This sulfosuccinic acid ester salt has an atomic group of sulfosuccinic acid at the center of the molecule, and is an ester-bonded sulfonate that has been esterified with the carboxylic acid power of this atomic group with various alcohols. becomes.
而して.このアルキル基Rの炭素数06〜C8のとき.
浸透性は極めて犬き<,Hの炭素数が小さいものは可溶
化性が太きい。Then. When this alkyl group R has 06 to C8 carbon atoms.
The permeability is extremely low, and those with a small number of H carbons have a high solubilization property.
一般には,RがC8の場合つまりエチルヘキシルが多く
,水,ベンゼンに可溶で硬水と酸に安定である。In general, when R is C8, ethylhexyl is common, and it is soluble in water and benzene, and stable in hard water and acids.
この発明において使用するスルフオ琥珀酸エステル塩と
しては,2−エチルへキシルスルフオ琥珀酸ナトリウム
およびn−オクチル琥珀酸ナトリウムなどであるがその
溶解度および湿潤力の試験結果を表−2に示す。The sulfosuccinic acid ester salts used in this invention include 2-ethylhexyl sodium sulfosuccinate and n-octyl sodium succinate, and the test results of their solubility and wetting power are shown in Table 2.
また,使用する微粒子状珪酸(コロイダルシリカ)の分
散粒子は,粒径10〜20mμの超微粒子であり,これ
は水を分散媒とした無水珪酸のコロイド溶液である。Further, the dispersed particles of fine particulate silicic acid (colloidal silica) used are ultrafine particles with a particle size of 10 to 20 mμ, and are a colloidal solution of silicic anhydride using water as a dispersion medium.
一般に.コロイド溶液として取扱れるものは.分散質を
なす粒子大いさが1〜100mμのものとされている。in general. What can be treated as a colloidal solution? The particle size of the dispersoid is said to be 1 to 100 mμ.
この発明に用いられる微粒子状珪酸の溶液は,pH9.
0〜10.0の範囲であれば,分散媒である水が蒸発し
ない限り安定であるが,珪酸ソーダや苛性ソーダのよう
なアルカリでpHが10,5以上にあげられた場合や食
塩や芒硝(硫酸ナトリウム)のような塩類や,その他多
価金属塩類を添加したときは,これらが,コロイダルシ
リカの安定性を保持している負の電荷に干渉して該電荷
を相殺するので,粒子は集合しゲル化を起す。The fine particulate silicic acid solution used in this invention has a pH of 9.
If it is in the range of 0 to 10.0, it will be stable as long as the dispersion medium water does not evaporate, but if the pH is raised to 10.5 or higher with an alkali such as sodium silicate or caustic soda, or if the pH is raised to 10.5 or higher with an alkali such as sodium silicate or caustic soda, or When salts such as sodium sulfate (sodium sulfate) or other polyvalent metal salts are added, they interfere with and cancel out the negative charge that maintains the stability of colloidal silica, causing the particles to aggregate. and causes gelation.
すなわち,電解質は,コロイダルシリカのゲル化を惹起
する傾向があり,ゲル化によって粒子相互が著しく強固
に結合し,集合体をつくる。That is, the electrolyte tends to induce gelation of colloidal silica, and the gelation causes the particles to bond extremely strongly to each other, forming aggregates.
従って,前記の陰イオン界面活性剤にこの微粒子状珪酸
溶液を加え,任意の倍率に稀釈した低濃度溶液は,元来
疎水性の気相一固相複合材科例えば,プラスチックフォ
ーム、ゴムフォーム繊維集合体等々の内部に深く浸透し
,次の工程のセメント,セメント一石こう系のペースト
を注入する作業が容易となる。Therefore, a low concentration solution obtained by adding this particulate silicic acid solution to the above-mentioned anionic surfactant and diluting it to an arbitrary ratio can be used for gas phase-solid phase composite materials that are originally hydrophobic, such as plastic foam, rubber foam fibers, etc. It penetrates deeply into the interior of the aggregate, etc., making it easier to inject cement and cement-gypsum paste in the next process.
セメント,セメント一石こう系のペーストの注入の方法
は,実施態様によって種々の例が考えられる。Various methods for injecting cement and cement-gypsum paste can be considered depending on the embodiment.
勿論.ペーストの粘度は,その注入方法を規定する。Of course. The viscosity of the paste dictates the method of its injection.
実施例−1
陰イオン活性剤として2エチルへキシルスルフオ琥珀酸
ナトリウム
10部,微粒子シリカ溶液(固形分20%)30部,水
60部(いずれも容量%)の配合比から成る溶液にポリ
ウレタンフォームを浸漬し,乾燥後,普通ボルトランド
セメント90部,半水石こう10部,水70部の配合比
率から成る固化材を注入した。Example-1 Polyurethane foam was added to a solution consisting of 10 parts of sodium 2-ethylhexylsulfosuccinate as an anionic activator, 30 parts of fine-particle silica solution (solid content 20%), and 60 parts of water (all percentages by volume). After soaking and drying, a solidifying agent consisting of 90 parts of ordinary Bortland cement, 10 parts of hemihydrate gypsum, and 70 parts of water was injected.
材令1日における圧縮強度は次のとおりである。The compressive strength at 1 day of age is as follows.
(i)ポリウレタンフォームを圧縮しないで注入した場
合 3.1kg/cm2
(ii>ポリウレタンを80%に圧縮しで注入した場合
1 0.0kg/cm2
たゾし圧縮強度は10%歪みの強度を示す。(i) When polyurethane foam is injected without compression 3.1 kg/cm2 (ii> When polyurethane is compressed to 80% and injected 1 0.0 kg/cm2 Tazoshi compressive strength indicates the strength at 10% strain .
実施例−2
陰イオン活性剤としてn−オクチルスルフオ琥珀酸ナト
リウム
10部、微粒子シリカ溶液20部、水70部、(いずれ
も容量%)の配合比から成る溶液にポリウレタンフォー
ムを浸漬し、乾燥後、普通ボルトランドセメント90部
.アルミナセメント10部,水70部の配合比率から成
る固化剤を注入した。Example 2 A polyurethane foam was immersed in a solution consisting of 10 parts of sodium n-octylsulfosuccinate as an anionic activator, 20 parts of a fine-particle silica solution, and 70 parts of water (all percentages by volume), and dried. Then, 90 parts of ordinary Bolland cement. A solidifying agent consisting of 10 parts of alumina cement and 70 parts of water was injected.
材令1週間における圧縮強度は次のとおりである。The compressive strength at one week of age is as follows.
(i)ポリウレタンフォームを圧縮しないで注入した場
合 5.2kg/cm2
(11)ポリウレタンフォームを80%圧縮しで注入し
た場合 17.okg/cm2
たゾし圧縮強度は10%歪みの強度を示す。(i) When polyurethane foam is injected without being compressed 5.2 kg/cm2 (11) When polyurethane foam is injected with 80% compression 17. okg/cm2 Tazoshi compressive strength indicates the strength at 10% strain.
応用例
第1図,第2図は,気相一固相複合材料1にポリウレタ
ンフォーム用い,これに前述の湿潤剤による含浸処理を
してシールド工事に応用した例である。APPLICATION EXAMPLE FIGS. 1 and 2 show an example in which polyurethane foam is used as the gas phase-solid phase composite material 1, which is impregnated with the above-mentioned wetting agent and applied to shield construction.
すなわち.シールド工事において.ポリウレタンフォー
ム1をセグメント4の背面に接着し,このポリウレタン
フォームに親水処理を施したセグメント4を.シールド
テール3内で組み立でる。In other words. In shield construction. Polyurethane foam 1 is adhered to the back of segment 4, and segment 4 is made by applying hydrophilic treatment to this polyurethane foam. It can be assembled inside Shield Tail 3.
而して.3のシールドプレート3′で圧縮され,泥水の
浸入を防止する。Then. It is compressed by the shield plate 3' of No. 3 to prevent muddy water from entering.
シールド機械の前進にともない,シールドテール3のシ
ールドプレート3′から出たポリウレタンフォーム1は
復元し,同時にセグメント4内側より,圧入装置5によ
って,セメントあるいはセメント一石こう系のペースト
2をポリウレタンフォーム1の組織内に注入する。As the shield machine moves forward, the polyurethane foam 1 that has come out of the shield plate 3' of the shield tail 3 returns to its original state, and at the same time, a cement or cement-gypsum paste 2 is applied to the polyurethane foam 1 from the inside of the segment 4 using a press-fitting device 5. Injected into tissue.
これによってペーストは.ポリウレタンフォーム1内に
浸透し,これを固化することにより,地山の肌落防止は
勿論のこと.全体の強度を増し.地山をゆるめることな
く地表面の沈下を防止できる。This will make the paste. By penetrating into the polyurethane foam 1 and solidifying it, it not only prevents the ground from falling off. Increase overall strength. Subsidence of the ground surface can be prevented without loosening the ground.
また,セグメントの接合面からの漏水も抑止できる。It also prevents water from leaking from the joint surfaces of the segments.
第1図はシールド工事の状態を示す説明図,第2図はそ
の横断面図である。
図中1は気相一固相複合材科であるポリウレタンフォー
ム,2はセメントあるいはセメント一石こウ系のペース
トである。Figure 1 is an explanatory diagram showing the state of the shield work, and Figure 2 is its cross-sectional view. In the figure, 1 is polyurethane foam, which is a gas phase-solid phase composite material, and 2 is cement or cement-gypsum paste.
Claims (1)
性剤および微粒状シリカ溶液を浸透せしめ,然る後,セ
メントあるいはセメント一石こう系のペーストを,前記
複合材科の組織内に注入してから固化することを特徴と
するプラスチックフォーム固化方法。 2 気相一固相複合材科に、熱硬化性または熱可塑性の
プラスチックフォームを適用する特許請求の範囲第1項
記載の気相一固相複合材科の固化方法。 3 気相一固相複合材料に.ポリウレタンフォーム又は
ポリスチレンフオームを適用する特許請求の範囲第1項
記載の気相一固相複合材科の固化方法。 4 気相一固相複合材科に,ゴムフォームを適用する特
許請求の範囲第1項記載の気相一固相複合材科の固化方
法。 5 気相一固相複合材科に.繊維集合体を適用する特許
請求の範囲第1項記載の気相一固相複合材料の固化方法
。[Scope of Claims] 1. An anionic activator and a fine granular silica solution are infiltrated in advance into an elastic gas phase-solid composite material, and then cement or cement-gypsum paste is applied to the composite material. A method for solidifying plastic foam, which is characterized by injecting it into the tissue of the material and then solidifying it. 2. A method for solidifying a vapor-solid composite material according to claim 1, wherein a thermosetting or thermoplastic plastic foam is applied to the vapor-solid composite material. 3. Gas phase-solid phase composite material. A method for solidifying a gas phase-solid composite material according to claim 1, wherein polyurethane foam or polystyrene foam is applied. 4. A method for solidifying a gas phase-solid phase composite material according to claim 1, wherein a rubber foam is applied to the gas phase-solid phase composite material category. 5 Gas phase-solid phase composite materials department. A method for solidifying a gas phase-solid phase composite material according to claim 1, wherein a fiber aggregate is applied.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP52137578A JPS588417B2 (en) | 1977-11-16 | 1977-11-16 | Solidification method of gas phase-solid phase composite material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP52137578A JPS588417B2 (en) | 1977-11-16 | 1977-11-16 | Solidification method of gas phase-solid phase composite material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5471077A JPS5471077A (en) | 1979-06-07 |
| JPS588417B2 true JPS588417B2 (en) | 1983-02-16 |
Family
ID=15201987
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP52137578A Expired JPS588417B2 (en) | 1977-11-16 | 1977-11-16 | Solidification method of gas phase-solid phase composite material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS588417B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60171214U (en) * | 1984-04-24 | 1985-11-13 | リンナイ株式会社 | rice cooker |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS574710A (en) * | 1980-06-13 | 1982-01-11 | Mitsubishi Mining & Cement Co | Manufacture of ceramic porous body |
| JP6393650B2 (en) * | 2014-03-31 | 2018-09-19 | 株式会社ジェイエスピー | Composite molded body |
-
1977
- 1977-11-16 JP JP52137578A patent/JPS588417B2/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60171214U (en) * | 1984-04-24 | 1985-11-13 | リンナイ株式会社 | rice cooker |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5471077A (en) | 1979-06-07 |
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