JPS5933381A - Anti-friction composition for shield excavation process - Google Patents

Anti-friction composition for shield excavation process

Info

Publication number
JPS5933381A
JPS5933381A JP14282682A JP14282682A JPS5933381A JP S5933381 A JPS5933381 A JP S5933381A JP 14282682 A JP14282682 A JP 14282682A JP 14282682 A JP14282682 A JP 14282682A JP S5933381 A JPS5933381 A JP S5933381A
Authority
JP
Japan
Prior art keywords
mineral
water
lubricant
oil
emulsifier
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP14282682A
Other languages
Japanese (ja)
Other versions
JPH0246076B2 (en
Inventor
Shigeru Iijima
茂 飯島
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.)
DKS Co Ltd
Original Assignee
Dai Ichi Kogyo Seiyaku 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 Dai Ichi Kogyo Seiyaku Co Ltd filed Critical Dai Ichi Kogyo Seiyaku Co Ltd
Priority to JP14282682A priority Critical patent/JPH0246076B2/en
Publication of JPS5933381A publication Critical patent/JPS5933381A/en
Publication of JPH0246076B2 publication Critical patent/JPH0246076B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/04Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
    • H01L21/18Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
    • H01L21/30Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
    • H01L21/31Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
    • H01L21/3205Deposition of non-insulating-, e.g. conductive- or resistive-, layers on insulating layers; After-treatment of these layers
    • H01L21/321After treatment
    • H01L21/3213Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer
    • H01L21/32133Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer by chemical means only
    • H01L21/32135Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer by chemical means only by vapour etching only
    • H01L21/32136Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer by chemical means only by vapour etching only using plasmas
    • H01L21/32137Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer by chemical means only by vapour etching only using plasmas of silicon-containing layers

Landscapes

  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Plasma & Fusion (AREA)
  • General Physics & Mathematics (AREA)
  • Manufacturing & Machinery (AREA)
  • Computer Hardware Design (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Power Engineering (AREA)
  • Excavating Of Shafts Or Tunnels (AREA)

Abstract

PURPOSE:To privide the titled composition consisting of (1) water, (2) a W/O type polymer emulsion which may contain an extreme-pressure additive, a lubricant, a mineral, animal or vegetable oil and an emulsifier and (3) a mineral substance, and exhibiting an excellent antifriction property. CONSTITUTION:The composition is prepared by blending (1) 100pts.wt. water, (2) 0.2-10pts.wt. W/O type polymer emulsion which may contain an extreme-pressure additive, a lubricant, a mineral, animal or vegetable oil and an emulsifier and (3) 2-20pts.wt. mineral substance (e.g. bentonite, clay or graphite). To obtain an antifriction material, a vinyl monomer is emulsified and dispersed in a mineral oil by use of an emulsifier, effecting emulsion polymerization in the presence of a catalyst and adding to the resultant polymer emulsion an extreme- pressure additive, a lubricant, a mineral, animal or vegetable oil which controls polymer concentration and increases lubricity, an emulsifier to enhance water dispersibility, etc.

Description

【発明の詳細な説明】 本発明は、シールド推進工法用減摩剤組成物に関する。[Detailed description of the invention] The present invention relates to a lubricant composition for shield propulsion construction method.

詳言すれば、水100重量部に対して。To be more specific, it is based on 100 parts by weight of water.

油中水型重合体エマルジョン、または予め極圧添加剤、
潤滑剤、鉱・動・植物油、乳化剤を配合した油中水型重
合体エマルジョン(0,2〜10重景部端量鉱物質(2
〜20重量部)、から構成されるシールド推進」二法用
減摩剤組成物を提供するものである。
Water-in-oil polymer emulsion, or pre-extreme pressure additives,
Water-in-oil polymer emulsion containing lubricants, mineral, animal, and vegetable oils, and emulsifiers (0.2-10%
~20 parts by weight).

シールド推進コニ法は、コンクリートや鋳鉄製管体を油
圧ジヤツキで地中に押し込み、電力線、電信電話線、上
下水道等の地下隨道を構築する工法であり、地表開削を
伴わないので、交通や商業活動への影響が比較的少ない
ことから多用されている。
The shield propulsion method is a construction method for constructing underground tunnels for power lines, telegraph and telephone lines, water and sewage lines, etc. by pushing concrete or cast iron pipes into the ground using hydraulic jacks, and since it does not involve excavation of the ground surface, it reduces traffic and It is widely used because it has relatively little impact on commercial activities.

この工法においては、地中に管体を押し込む工法である
ため、推進した管体本数(距離)に応じて押し込みに要
する推進力は増大するので、管体や推進ジヤツキを取り
付けた反力壁の強度の面から推進距離は限定されるとい
う問題がある。
In this construction method, the pipes are pushed into the ground, so the driving force required for pushing increases depending on the number (distance) of the pipes pushed, so the reaction wall with the pipes and propulsion jacks There is a problem in that the propulsion distance is limited due to strength.

推進されるべき距離は、長いほど施工上の能率は良好な
ので、距離延長を目的に推進距離に応じて、推進管の間
に数個の中間ジヤツキを設置して推進力を増加させる方
法も採用されている。
The longer the distance to be propelled, the better the construction efficiency, so in order to extend the distance, we have also adopted a method of increasing the propulsive force by installing several intermediate jacks between the propulsion tubes depending on the distance of propulsion. has been done.

しかし、中間ジヤツキの設置は推進操作が煩雑となり、
作業効率を著しく低下させるので、多数の中間ジヤツキ
設置は好ましくない。
However, installing an intermediate jack makes the propulsion operation complicated,
It is undesirable to install a large number of intermediate jacks because it significantly reduces work efficiency.

他の方法として減摩剤の注入があり、減摩剤として、水
にベントナイト、CMC(カルボキシメチルセルローズ
)、ポリアクリル酸ソーダ。
Another method is to inject a lubricant, such as bentonite, CMC (carboxymethyl cellulose), or sodium polyacrylate in water.

界面活性剤、鉱物油等を分散させた高粘稠液体を推進管
と他山との間隙に注入してすベリ抵抗を減少させる方法
が特公昭4fl−1906号公報に提案されている。
Japanese Patent Publication No. 4FL-1906 proposes a method for reducing slippage resistance by injecting a highly viscous liquid in which a surfactant, mineral oil, etc. are dispersed into the gap between the propulsion tube and another mountain.

この方法は、推進力の減少に比較的高い効果を期待でき
るが、数種類の材料を調合するので、減摩剤の調製か煩
雑である。また、減摩剤は高粘稠性であることから、減
摩剤調製専用の溶解機が必要であり、かつCMCやポリ
アクリル酸ソーダ等の糊剤は粉末状品を用いることから
、完全溶解には長時間を要し、不充分な溶解状態では減
摩効果が大幅に低下する等の欠点があり、調合が容易で
短時間で調製でき、満足すべき減摩効果を有する減摩剤
組成物の開発が待たれていた。
Although this method can be expected to be relatively effective in reducing the propulsion force, it is complicated to prepare the lubricant because several types of materials are mixed. In addition, since the lubricant has a high viscosity, a dissolving machine dedicated to preparing the lubricant is required, and since glues such as CMC and sodium polyacrylate are powdered, they are completely dissolved. It takes a long time to prepare the lubricant, and if the dissolution state is insufficient, the anti-friction effect is significantly reduced. The development of something was awaited.

本発明者は、これら減摩剤組成物に関して、鋭意研究の
結果、水100重量部に対して、油中木型重合体エマル
ジョン、または予め極圧添加剤、潤滑剤、鉱動植物浦、
乳化剤を配合した油中木型重合体エマルジョン(0,2
〜10重鼠部重職鉱物質(2〜20重量部)から構成さ
れるシールド推進工法用減摩剤組成物を提供するに至っ
たものである。
As a result of intensive research regarding these anti-friction agent compositions, the present inventors have found that, with respect to 100 parts by weight of water, a wood-in-oil polymer emulsion, or an extreme pressure additive, a lubricant, mineral fauna and flora, etc.
Wood-in-oil polymer emulsion containing an emulsifier (0,2
We have now provided a lubricant composition for shield propulsion construction, which is comprised of ~10 parts by weight of minerals (2 to 20 parts by weight).

本発明における減摩剤は、水分散液としてまたは鉱物質
との併用で使用されるが、調合は極めて簡単であり、ま
た水に減摩剤を添加すると、乳化剤の作用により容易に
水中へ分散し短時間で高粘稠液が得られ、優れた減摩効
果を有する減摩剤を得ることができ、従来から使用され
てきた減摩剤の欠点を完全に解消したものである。
The anti-friction agent in the present invention is used as an aqueous dispersion or in combination with a mineral substance, but it is extremely easy to prepare, and when the anti-friction agent is added to water, it is easily dispersed in water due to the action of an emulsifier. A highly viscous liquid can be obtained in a short period of time, and a lubricant having an excellent antifriction effect can be obtained, completely eliminating the drawbacks of conventionally used lubricants.

本発明における減摩剤は、鉱物油中に、ビニル系モノマ
ーを乳化剤で乳化分散させた後、触媒を添加して乳化重
合し、 ti圧添加剤や潤滑剤あるいはポリマー濃度の
調整と潤滑性を増加させる鉱物油、動植物油や水分散性
を高める乳化剤等を添加し、て調整できる。
The lubricant used in the present invention is produced by emulsifying and dispersing a vinyl monomer in mineral oil using an emulsifier, and then adding a catalyst to carry out emulsion polymerization to adjust the concentration of Ti pressure additives, lubricants, or polymers, and to improve lubricity. It can be adjusted by adding mineral oil, animal or vegetable oil, or an emulsifier to increase water dispersibility.

この乳化重合には、特公昭52−39417号公報、お
よび米国特許第3171805号明細書等に示された乳
化重合方法が使用できる。
For this emulsion polymerization, the emulsion polymerization method disclosed in Japanese Patent Publication No. 52-39417, US Pat. No. 3,171,805, etc. can be used.

本発明の重合時に使用する鉱物油には、1〜ルエン、灯
油、軽油、ナフサ、流動パラフィン等が使用できる。
As the mineral oil used in the polymerization of the present invention, 1 to toluene, kerosene, light oil, naphtha, liquid paraffin, etc. can be used.

重合終了後、ポリマー濃度の調整と潤滑性増加を目的に
添加される鉱物油には、前記鉱物油および動植物油とし
ては比較的低融点のウールグリース、鯨油等や大豆油、
ナタネ油、ヤシ油、パーム油等が使用できる。
After completion of polymerization, the mineral oil added for the purpose of adjusting the polymer concentration and increasing lubricity includes wool grease, whale oil, etc., which have a relatively low melting point among the mineral oils and animal and vegetable oils, soybean oil, etc.
Rapeseed oil, coconut oil, palm oil, etc. can be used.

ビニル系モノマーには、アクリルアミド、アクリル酸、
アクリル酸メチル、メタクリル酸、メタクリル酸メチル
、無水マレイン酸等の貼独および共重合物であって5重
合物は水溶性であるものが使用できる。
Vinyl monomers include acrylamide, acrylic acid,
Polymers and copolymers of methyl acrylate, methacrylic acid, methyl methacrylate, maleic anhydride, etc., and the pentapolymers are water-soluble.

重合時の乳化剤には1石油スルフォン酸塩、アルキルお
よびアルキルアリルスルフォン酸塩、アルキルおよびア
ルキルアリルエ1−キシレート、ソルビタン脂肪酸エス
テル、ポリアルキレングリコールエーテル等が使用でき
る。また、極圧添加剤、潤滑剤としては、塩素化脂肪酸
、塩素化脂肪酸エステル、硫化脂肪、硫化脂肪酸、有機
モリブデン化合物、有機燐化合物、ポリアルキレングリ
コール、石油スルホン酸塩等を挙げることができる。
As the emulsifier during polymerization, 1-petroleum sulfonate, alkyl and alkylaryl sulfonate, alkyl and alkylaryl 1-xylate, sorbitan fatty acid ester, polyalkylene glycol ether, etc. can be used. Examples of extreme pressure additives and lubricants include chlorinated fatty acids, chlorinated fatty acid esters, sulfurized fats, sulfurized fatty acids, organic molybdenum compounds, organic phosphorus compounds, polyalkylene glycols, petroleum sulfonates, and the like.

重合触媒は、油溶性であることが好ましいが、水不溶で
も触媒作用を充分に有するものであれば、制限はなく、
一般に2.2′−アゾヒスイソブチロニトリロやベンジ
ルパーオキサイド等が使用される。
The polymerization catalyst is preferably oil-soluble, but there is no restriction as long as it has sufficient catalytic activity even if it is water-insoluble.
Generally, 2,2'-azohisisobutyronitrilo, benzyl peroxide, etc. are used.

油中水型重合体エマルジョン中の重合体濃度は、一般に
10〜60%で重合できるが、重合後鉱物油や動植物油
を添加して重合体濃度を適宜希釈することができる。重
合終了後、潤滑剤や極圧添加剤、乳化剤等も適宜添加す
ることもでき、また重合に悪影響を与えない範囲で重合
時に添加することもできる。
The polymer concentration in the water-in-oil polymer emulsion can generally be polymerized at 10 to 60%, but after polymerization, mineral oil or animal or vegetable oil can be added to dilute the polymer concentration as appropriate. After the polymerization is completed, lubricants, extreme pressure additives, emulsifiers, etc. can be added as appropriate, and they can also be added at the time of polymerization to the extent that they do not adversely affect the polymerization.

本発明における減摩剤は、重合体濃度が高くても低粘性
を保持しているので、取扱いが容易であり、減摩剤組成
物を調製する際、減摩剤を水に添加すると、減摩剤中の
乳化剤が油類を微細粒子として分散させるので、重合体
も油類と共にm細に分散するため、重合体の塊状化を起
こし鍾く、短時間で溶解させることができる。
The lubricant of the present invention maintains a low viscosity even at high polymer concentrations, so it is easy to handle, and when the lubricant is added to water when preparing a lubricant composition, it reduces Since the emulsifier in the lubricant disperses the oil as fine particles, the polymer is also dispersed into fine particles along with the oil, which prevents the polymer from clumping and can be dissolved in a short time.

また、組成物中の潤滑剤や極圧摩擦減少剤等も同時に分
散、溶解するので、短時間で容易に減摩剤組成物が調製
できる。
Further, since the lubricant, extreme pressure friction reducing agent, etc. in the composition are simultaneously dispersed and dissolved, the friction reducing agent composition can be easily prepared in a short time.

本発明における減摩剤は、?ltに水に分散させただけ
でも減摩効果を発揮できるが、 ・般には減摩剤コス1
〜の低減と加圧下で注入した減摩剤が地山表面で泥膜を
形成し、逸失を少くすることを目的として、ベントナイ
1−1粘土、グラフアイ1−等の鉱物質を併用すること
が好ましい。
What is the anti-friction agent in the present invention? Although anti-friction effects can be exerted simply by dispersing it in water, ・In general, anti-friction agents cost 1
Mineral materials such as Bentonai 1-1 clay and Grapheye 1- are used together with the aim of reducing the amount of friction and reducing the amount of lubricant injected under pressure to form a mud film on the ground surface and reduce loss. is preferred.

以下に本発明の実施例を示すが5本発明はこれらの実施
例に限定されるものでない。
Examples of the present invention are shown below, but the present invention is not limited to these Examples.

(実施例中の部、%はすべで重量部、重量%を示す。) 実施例1 1W拌装置、温度計、窒素導入管を備えたガラス製反応
容器に軽油20gとオレイルエトキシレーh(p  3
.5)2.5gとソルビタンモノオレー1−2.5gを
添加して溶解した後、アクリル酸モノマー36 F、を
水50gに溶解し、12gのカセイソーダで中和したア
クリル酸ソーダモノマー水溶液を調製し、反応容器に攪
拌しながら添加した。続いて窒素ガスを導入して反応容
器内の空気を窒素と置換した後、アセトンに溶解りまた
アゾビスイソブチロニ1−リル0.01gを添加する。
(All parts and % in the examples indicate parts by weight and % by weight.) Example 1 20 g of light oil and oleyl ethoxylene h (p 3
.. 5) After adding and dissolving 2.5 g and 1-2.5 g of sorbitan monoole, acrylic acid monomer 36 F was dissolved in 50 g of water and neutralized with 12 g of caustic soda to prepare a sodium acrylate monomer aqueous solution. , was added to the reaction vessel with stirring. Subsequently, nitrogen gas is introduced to replace the air in the reaction vessel with nitrogen, and then 0.01 g of azobisisobutyroni-1-lyl dissolved in acetone is added.

反応容器を7IO℃に保持しながら3時間攪拌すること
で、アクリル酸ソーダの油中水型重合体エマルジョン(
A)を得た。
A water-in-oil polymer emulsion of sodium acrylate (
A) was obtained.

極限粘度は〔η〕は11.6(2N−Nao830℃)
であった。
The intrinsic viscosity [η] is 11.6 (2N-Nao830℃)
Met.

実施例2 実施例1に準じ、ノルマルパラフィン(日鉱油化曲N 
−120) 100gとソルビタンモノラウレート録を
添加して溶解した後、アクリル酸モノマ−18gとアク
リルアミドモノマー17.3gを水50gに溶解し8g
のカセイソーダで中和した。
Example 2 According to Example 1, normal paraffin (Nippon Yuka Koku N
-120) After adding and dissolving 100g of sorbitan monolaurate, 18g of acrylic acid monomer and 17.3g of acrylamide monomer were dissolved in 50g of water and 8g
Neutralized with caustic soda.

続いて窒素ガスを導入して空気を窒素と置換した後、ア
セ1−ンに溶解したアゾビスイソブチロニ1−リロ0.
01gを添加する。
Subsequently, nitrogen gas was introduced to replace the air with nitrogen, and then azobisisobutyroni-1-lilo0.
Add 01g.

反応容器を40℃に保持しながら3時間攪拌することで
、アクリル酸ソーダとアクリルアミドとの油中水型共重
合体エマルジョン(B)を得た。
A water-in-oil copolymer emulsion (B) of sodium acrylate and acrylamide was obtained by stirring the reaction container at 40° C. for 3 hours.

極限粘度は〔η〕は14.6(2N−Naoll 30
”clテあった。
The intrinsic viscosity [η] is 14.6 (2N-Naoll 30
“There was a club.

実施例3 実施例1および同2で得られた重合体エマルジョン(A
)または(B)に油類、乳化剤、横圧添加剤を混合して
次の減摩剤(1)〜(4)を調製した。
Example 3 Polymer emulsion (A
) or (B) with oils, emulsifiers, and lateral pressure additives to prepare the following lubricants (1) to (4).

減摩剤(1) 重合体エマルジョン(A)       50部大豆白
絞油           4゜5ULFOL  50
0                       1
0(松材石油KK製石油スルフォン酸ソーダ)減摩剤(
2) 重合体エマルジョン(^)50部 大豆白絞油           4゜エパン720 
             10(第一]二業製薬にに
製ポリプロピレングリコールポリエチレングリコールエ
ーテル) 減摩剤(3) 重合体エマルジョン(1’3)       50部6
0スピンドル油          45プライサーフ
A208B          5(第一工業製薬にに
製アルキルエトキシレー1〜リン酸エステル) 減摩剤(4) 重合体エマルジョン(B)       95部ラウリ
ルアルコール        5実施例4 水100部をプロペラ型羽根250rpmで攪拌しなが
らベントナイト250メツシュ品(王立ベンl−ナイ1
−」、業■製)10部を添加して3分間撹11!シて分
散させる。
Antifriction agent (1) Polymer emulsion (A) 50 parts White soybean oil 4゜5ULFOL 50
0 1
0 (Sodium petroleum sulfonate manufactured by Matsuzai Oil KK) Anti-friction agent (
2) Polymer emulsion (^) 50 parts soybean white squeezed oil 4° Epan 720
10 (Daiichi) Polypropylene glycol polyethylene glycol ether manufactured by Nigyo Pharmaceutical Co., Ltd.) Anti-friction agent (3) Polymer emulsion (1'3) 50 parts 6
0 Spindle oil 45 Plysurf A208B 5 (Alkyl ethoxylate 1-phosphate ester manufactured by Daiichi Kogyo Seiyaku) Anti-friction agent (4) Polymer emulsion (B) 95 parts lauryl alcohol 5 Example 4 100 parts of water was added to the propeller Bentonite 250 mesh product (Royal Bentonite 1
-", manufactured by Kogyo ■) and stirred for 3 minutes 11! and disperse.

次に攪拌を続けながら、所定量の本発明域jf剤、乳化
剤等を添加し、減摩剤組成物を調製して経時による粘性
変化を旧+1EOME1’[ER(NR阿−2010型
、不動工業潤製)にて測定した。測定は20°Cにおい
て100mQのビーカーに減摩剤組成物100mQ採り
、直径30m/mの円盤(7,06cJ)を50m/m
/minの速度で■・降させ、その時円盤にかかる荷重
を記録旧から読み取りゲル強度とした。
Next, while continuing to stir, a predetermined amount of the jf agent of the present invention, an emulsifier, etc. is added to prepare a lubricant composition, and the viscosity change over time is adjusted to (Junsei). The measurement was carried out at 20°C by placing 100 mQ of the anti-friction agent composition in a 100 mQ beaker, and placing a disk (7,06 cJ) with a diameter of 30 m/m at 50 m/m.
The gel strength was determined by reading the load applied to the disk at that time from the old record.

また、標準砂(豊浦珪石工業it!litりを水て湿め
らせて30m/mの厚さに突き固めた上に60分間経過
後の」二記で調製した組成物をIOm/mの厚さに塗布
し、この」−にコンクリ−1〜製ブロツク(幅100m
/m、高さ100m/m、長さ200m/+n)を乗せ
、直ちにバネ秤で引き、その時の最大静止摩擦力を測定
した。その結果を第1表に示す。
In addition, the composition prepared in section 2 was added to standard sand (Toyoura Silica Stone Industry IT!L) moistened with water and tamped to a thickness of 30 m/m, and after 60 minutes passed. Apply it to a thickness and apply it to a concrete block (width 100m).
/m, height 100m/m, length 200m/+n), and immediately pulled it with a spring scale to measure the maximum static friction force at that time. The results are shown in Table 1.

第1表に示す様に本発明減摩剤組成物は、棒めて短時間
で調製することができ、一般的に使用さ、hている対照
例と同等以上の減摩効果も示すことが判る。
As shown in Table 1, the anti-friction composition of the present invention can be prepared in a short time and exhibits an anti-friction effect equal to or better than that of the commonly used control example. I understand.

実施例5 機械式土圧対抗型泥水加圧セミシールド掘進機(外径2
8 f)(l m / m )で滞水砂層を150m1
li!した。
Example 5 Mechanical earth pressure counter-type mud water pressurizing semi-shield excavator (outer diameter 2
8 f) (l m / m ) with a water retention sand layer of 150 m1
li! did.

減摩剤組成物として水1 fJ f)部に対し戸、−V
ヘントナイl−25(Iメツシュ品10部と実施例1で
得た重合体エマルジョン(A)1部を添加しで調製した
減摩剤組成物を充填率150%で注入し、た結果、計画
堆力2401)l−ンに吋し最大推力185(ll・ン
と推進抵抗を減少させることができた。
-V for 1 fJ f) part of water as lubricant composition
A lubricant composition prepared by adding 10 parts of Hetonai I-25 (I mesh product) and 1 part of the polymer emulsion (A) obtained in Example 1 was injected at a filling rate of 150%, and as a result, the planned deposit was It was possible to reduce the propulsion resistance to a maximum thrust of 185 (ll) by increasing the force to 2,401) l.

出願人 第一1.業製薬株式会社applicant 11. Industrial Pharmaceutical Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] 水100重量部に対して、油中水型重合体エマルジョン
、または予め極圧添加剤、潤滑剤、鉱動植物油、乳化剤
を配合した油中木型重合体エマ
A water-in-oil polymer emulsion or a wood-in-oil polymer emulsion prepared by adding extreme pressure additives, lubricants, mineral, animal and vegetable oils, and emulsifiers to 100 parts by weight of water.
JP14282682A 1982-08-17 1982-08-17 SHIIRUDOSUISHINKOHOYOGENMAZAISOSEIBUTSU Expired - Lifetime JPH0246076B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14282682A JPH0246076B2 (en) 1982-08-17 1982-08-17 SHIIRUDOSUISHINKOHOYOGENMAZAISOSEIBUTSU

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14282682A JPH0246076B2 (en) 1982-08-17 1982-08-17 SHIIRUDOSUISHINKOHOYOGENMAZAISOSEIBUTSU

Publications (2)

Publication Number Publication Date
JPS5933381A true JPS5933381A (en) 1984-02-23
JPH0246076B2 JPH0246076B2 (en) 1990-10-12

Family

ID=15324512

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14282682A Expired - Lifetime JPH0246076B2 (en) 1982-08-17 1982-08-17 SHIIRUDOSUISHINKOHOYOGENMAZAISOSEIBUTSU

Country Status (1)

Country Link
JP (1) JPH0246076B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01235794A (en) * 1988-03-17 1989-09-20 Mitsui Saianamitsudo Kk Propelling construction
EP1795700A1 (en) * 2005-11-26 2007-06-13 F & B GmbH Feuerschutz & Baustofftechnik Shield tail sealing paste
JP2012131884A (en) * 2010-12-21 2012-07-12 Shimizu Corp Foaming agent for foam shielding method and method for using the same
CN112592701A (en) * 2020-12-22 2021-04-02 广州江盐化工有限公司 Oil-based drilling fluid based on chlorinated fatty acid ester and preparation method and application thereof

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01235794A (en) * 1988-03-17 1989-09-20 Mitsui Saianamitsudo Kk Propelling construction
EP1795700A1 (en) * 2005-11-26 2007-06-13 F & B GmbH Feuerschutz & Baustofftechnik Shield tail sealing paste
JP2012131884A (en) * 2010-12-21 2012-07-12 Shimizu Corp Foaming agent for foam shielding method and method for using the same
CN112592701A (en) * 2020-12-22 2021-04-02 广州江盐化工有限公司 Oil-based drilling fluid based on chlorinated fatty acid ester and preparation method and application thereof

Also Published As

Publication number Publication date
JPH0246076B2 (en) 1990-10-12

Similar Documents

Publication Publication Date Title
CA1246850A (en) Liquid fluid loss control additive for oil field cements
US4325861A (en) Rapidly dissolved water-soluble polymer composition
CA1317099C (en) Compositions for freeing jammed drill pipes
NO861373L (en) APPLICATION OF MONO- AND POLYALKYLENE GLYCOLETERS AS MENTALS FOR THE RELEASE OF LOCKED DRILLS.
US6849582B2 (en) Method of oil/gas well stimulation
CN112592701B (en) Oil-based drilling fluid based on chlorinated fatty acid ester and preparation method and application thereof
US4171337A (en) Process for forming ceramic bodies employing aqueous lubricant
CN106753315A (en) A kind of temperature control type becomes mucic acid and preparation method thereof
JP2823619B2 (en) A novel aqueous emulsion copolymer for improving petroleum fluidity
RU2231534C2 (en) Drilling fluid and a method for preparation thereof
JPS5933381A (en) Anti-friction composition for shield excavation process
CN106147729A (en) A kind of oil base drilling fluid and preparation method thereof
JPS6252786B2 (en)
CN115710330A (en) Preparation method of polymer microsphere/graphene oxide emulsion for profile control and flooding
CN114479764B (en) Polycarboxylic acid high-efficiency dust suppressant and preparation method and application thereof
JPH0586831B2 (en)
WO2017087665A1 (en) Biodegradable soil conditioner
CN106753723B (en) Lubricant for pipeline earth moving machine and preparation method thereof
US20140140771A1 (en) Chemical Method and Composition for Soil Improvement
JP2534208B2 (en) Propulsion method
JPH1192565A (en) Oil-base dispersion of water-absorbent resin
JPS5827774A (en) Driving method of construction reducing frictional force between soil and driving pipe
JP2003327989A (en) Powder lubricant and mud adding material for civil engineering use containing the same
JPS60133084A (en) Slurrying material composition
JP3132148B2 (en) Thickening method