JPS6238399B2 - - Google Patents
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- Publication number
- JPS6238399B2 JPS6238399B2 JP13478079A JP13478079A JPS6238399B2 JP S6238399 B2 JPS6238399 B2 JP S6238399B2 JP 13478079 A JP13478079 A JP 13478079A JP 13478079 A JP13478079 A JP 13478079A JP S6238399 B2 JPS6238399 B2 JP S6238399B2
- Authority
- JP
- Japan
- Prior art keywords
- polymer
- mud
- muddy water
- soil
- water
- 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
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- Agricultural Chemicals And Associated Chemicals (AREA)
Description
【発明の詳細な説明】
本発明は、土木、建築工事の基礎工事におい
て、天然の有機系高分子や、その変成物、たとえ
ば、カルボキシメチルセルロース(CMC)、カル
ボキシメチルデンプン(CMS)、トラガントガム
を含む泥水を用いて地盤を掘削する泥水工法で使
用するポリマー泥水の変質腐敗防止剤に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention uses natural organic polymers and modified products thereof, such as carboxymethyl cellulose (CMC), carboxymethyl starch (CMS), and gum tragacanth, in the foundation work of civil engineering and construction works. This invention relates to an anti-corrosion agent for polymer muddy water used in the muddy method of excavating the ground using muddy water.
従来、本工法では地盤掘削時にベントナイトを
他の添加剤とともに水に懸濁させた、いわゆるベ
ントナイト泥水が使用されてきた。 Conventionally, this method has used so-called bentonite slurry, which is made by suspending bentonite in water along with other additives during ground excavation.
ところが近年、そのベントナイトが不足し、代
替物の開発が急がれてきた。ベントナイトの高い
膨潤性、微粒子性、または塩基交換性などの特性
を合わせもつた代替物ということで、このポリマ
ー泥水が開発されるに至つたのである。 However, in recent years, there has been a shortage of bentonite, and there has been an urgent need to develop a substitute. This polymer slurry was developed as a substitute for bentonite, which has the characteristics of high swelling, fine particle size, and base exchangeability.
しかしながら、このポリマー泥水のいくつかの
特徴は、混入する土粒子とポリマーの結合した土
粒子・ポリマー複合体の特質によるものであり、
土粒子との相互作用の顕著でないベントナイト泥
水とは根本的に異なるものであることが判明し
た。たとえば、(1)現場泥水では5%程度の掘削土
が泥水中に混入するが、ポリマー泥水では少量の
土の混入によつて造壁性が著しく改善されるこ
と、(2)ポリマー泥水の造壁性はポリマー濃度、お
よび混入土量とポリマー濃度の比によつて支配さ
れ、脱水量もこのポリマー濃度の比によつて変化
する。(3)ポリマー泥水はセメントの混入によつて
造壁性が低下するが、ベントナイト泥水のような
ゲル化はしない。ポリマー泥水はベントナイト泥
水に比べて耐セメント性が高く、耐セメント性は
ポリマーと混入掘削土の比に支配される。ところ
が、(4)ポリマー泥水は長期間放置すると、造壁
性、粘度が低下して変質する。この変質は、高温
で著しく、また、混入土の多いものほど著しい。
この原因は主として混入土中の微生物の酵素作用
によるポリマーの加水分解に基づくものであり、
変質防止剤を添加することによつて変質を防止す
ることができる。(5)ポリマー泥水の造壁性、耐セ
メント性、変質抵抗性のいずれも泥水中のポリマ
ーと掘削土粒子の存在割合によつて支配される。
このことはポリマー泥水の性状が土粒子・ポリマ
ー複合体の性状、特にポリマー被覆層の厚さに関
係していることを示唆している。 However, some of the characteristics of this polymer mud are due to the characteristics of the soil particle/polymer composite, which is a combination of soil particles and polymer.
It was found that this is fundamentally different from bentonite mud, which does not interact significantly with soil particles. For example, (1) about 5% of excavated soil is mixed into muddy water in the field, but in polymer muddy water, the wall-building property is significantly improved by the addition of a small amount of soil; (2) the construction property of polymeric muddy water is Wall properties are controlled by the polymer concentration and the ratio of the amount of mixed soil to the polymer concentration, and the amount of water removed also changes depending on the ratio of the polymer concentration. (3) Although the wall-building properties of polymer muds deteriorate due to the inclusion of cement, they do not gel like bentonite muds. Polymer mud has higher cement resistance than bentonite mud, and the cement resistance is controlled by the ratio of polymer to mixed excavated soil. However, (4) if polymer mud is left for a long period of time, its wall-forming properties and viscosity decrease and its quality changes. This alteration is remarkable at high temperatures, and the more soil is mixed in.
The cause of this is mainly due to the hydrolysis of polymers by the enzymatic action of microorganisms in the contaminated soil.
Deterioration can be prevented by adding a deterioration inhibitor. (5) The wall-building properties, cement resistance, and alteration resistance of polymer mud are all controlled by the proportion of polymer and excavated soil particles in the mud.
This suggests that the properties of the polymer mud are related to the properties of the soil particle/polymer composite, especially the thickness of the polymer coating layer.
以上述べたポリマー泥水の特性の中で、欠点と
も言うべき泥水の変質についてさらに詳しく記述
する。本工法において、掘削孔内に、このポリマ
ー泥水を満たし掘削終了後、コンクリート打設の
際に泥水は回収され貯泥槽に保存される。この泥
水は、次の孔を掘削する時に再使用され、くり返
し使用可能であるが(泥水の転用回数は、ベント
ナイト泥水の場合の2倍以上になるが)何回も使
用する内に、特に夏季に施工した現場では、泥水
が黒味を帯び、腐敗臭を発し、泥壁形成能、粘性
などの泥水の性能が低下する現象がみられる。
(ただし、秋から冬にかけて施工された現場では
工事期間中、目立つた変質は認められない。)こ
のことは、特に高温では泥水の貯蔵日数とともに
土粒子・ポリマー複合体のポリマーが酵素作用に
より離脱し、低分子化していることを示唆し、一
種の加水分解が起つていると推定される。その酵
素は、大気中、或いは、混入土中のバクテリア等
の微生物が基質であるグルカン等のポリマーの存
在下で誘導生産したものと考えられる。 Among the properties of polymer mud described above, the alteration of mud water, which can be called a drawback, will be described in more detail. In this construction method, the borehole is filled with this polymer muddy water, and after the completion of excavation, the muddy water is collected during concrete pouring and stored in a mud storage tank. This muddy water is reused when drilling the next hole and can be used repeatedly (although the number of times the muddy water is diverted is more than twice that of bentonite muddy water). At construction sites, muddy water has a dark tinge, gives off a putrid odor, and the performance of the muddy water, such as its ability to form mud walls and viscosity, has deteriorated.
(However, no noticeable deterioration was observed during the construction period at sites where construction was carried out from autumn to winter.) This means that, especially at high temperatures, the polymers in the soil particle-polymer complex are released by enzyme action as the mud water is stored for several days. This suggests that the molecular weight has been reduced, and it is presumed that a type of hydrolysis is occurring. It is thought that the enzyme is induced and produced by microorganisms such as bacteria in the air or contaminated soil in the presence of a polymer such as glucan as a substrate.
これまでに、このポリマー泥水に有効な変質防
止剤として、サリチル酸などが知られているが
(特開昭50−125510号による)、混入土の種類や季
節によつては、泥水粒度の低下、泥水中の生菌数
の増加等、変質と思われる現象がみうけられた。 So far, salicylic acid has been known as an effective deterioration prevention agent for this polymer mud (according to Japanese Patent Application Laid-Open No. 125510/1983), but depending on the type of soil mixed in and the season, it may reduce the grain size of the mud, Phenomena that appeared to be alteration were observed, such as an increase in the number of viable bacteria in the muddy water.
そこで、本発明者らは、混入土の種類や季節を
問わず、より強力な作用を示す変質防止剤を種々
検討した結果、ヘキサヒドロ−1,3,5−トリ
ス−(2−ヒドロキシエチル)−s−トリアジン、
1,2−ベンズイソチアゾロン−3−オン、およ
び5−クロロ−2−メチル−4−イソチアゾリン
−3−オンと2−メチル−4−イソチアゾリン−
3−オンとの混合物の1種以上の有効成分とする
ことを特徴とする泥水工法用防腐剤の発明を完成
するに至つた。これらの化合物をポリマー泥水調
製の際に(CMCと粒性土と水を混合撹拌)添加
することによつて腐敗を抑えることができること
を見い出したものである。防腐剤の添加濃度は
0.01%以上添加すれば充分である。 Therefore, the present inventors investigated various deterioration prevention agents that exhibit stronger effects regardless of the type of mixed soil or the season, and found that hexahydro-1,3,5-tris-(2-hydroxyethyl)- s-triazine,
1,2-benzisothiazolin-3-one, and 5-chloro-2-methyl-4-isothiazolin-3-one and 2-methyl-4-isothiazolin-3-one.
The present inventors have completed the invention of a preservative for muddy water construction methods, which is characterized in that it is one or more active ingredients in a mixture with 3-one. We have discovered that rot can be suppressed by adding these compounds when preparing polymer slurry (mixing and stirring CMC, granular soil, and water). The concentration of preservative added is
It is sufficient to add 0.01% or more.
これらの薬剤を用いると何ら泥水の機能を損な
わず(粘度、生菌数など)作業性はきわめて良好
である。 When these chemicals are used, workability is extremely good without impairing the functions of muddy water (viscosity, number of viable bacteria, etc.).
次に本発明の要旨を実施例によつて説明する。 Next, the gist of the present invention will be explained using examples.
1 生菌数測定試験例
Γ 滅菌ピペツト
Γ 滅菌シヤーレ
Γ 滅菌希釈水(蒸留水)
Γ 培養基:ブドウ糖ブイヨン寒天培地(PH
7)…オートクレープ滅菌を施したもの。1 Example of viable bacteria count measurement test Γ Sterile pipette Γ Sterile shear dish Γ Sterile dilution water (distilled water) Γ Culture medium: Glucose bouillon agar medium (PH
7)...Sterilized by autoclave.
以上のものを準備しておき、サンプル液を上記
ピペツトと希釈水にて適宜、希釈する。希釈した
液の1mlをシヤーレにとつて、40℃位に冷やした
培地を加え、良く撹拌して固化させる。 Prepare the above items and dilute the sample solution appropriately with the pipette and dilution water. Transfer 1 ml of the diluted solution to a petri dish, add the culture medium cooled to around 40°C, and stir well to solidify.
37℃にて2日間培養した後、シヤーレに発生し
たコロニーを数え、それに希釈倍数をかけて生菌
数とする。 After culturing at 37°C for 2 days, count the colonies that have developed on the shears and multiply by the dilution factor to obtain the number of viable bacteria.
2 粘度測定試験例
サンプル液を28℃の恒温槽につけて、回転粘度
計を用いて測定する。2. Viscosity measurement test example Place the sample solution in a constant temperature bath at 28°C and measure using a rotational viscometer.
実施例 1
ポリマーとしてCMC0.5%、湿潤土5%を添加
し水を加えたものをミキサーにて継粉が見当らな
くなるまで充分溶解する。これに変質防止剤とし
て、ヘキサヒドロ−1,3,5−トリス(2−ヒ
ドロキシエチル)−s−トリアジンを0.03%量添
加し、28℃にて静置保存する。保存中の泥水の腐
敗状況を経日的に生菌数と粘度の変化により検討
する。Example 1 0.5% CMC and 5% wet soil were added as polymers, water was added, and the mixture was sufficiently dissolved in a mixer until no joint powder was found. To this was added 0.03% hexahydro-1,3,5-tris(2-hydroxyethyl)-s-triazine as a deterioration inhibitor, and the mixture was stored at 28°C. The state of decay of muddy water during storage is examined by changes in the number of viable bacteria and viscosity over time.
実施例 2
その他の薬剤として、1,2−ベンズイソチア
ゾロン−3−オン0.01%、および0.04%。Example 2 Other drugs include 1,2-benzisothiazolone-3-one 0.01% and 0.04%.
5−クロロ−2−メチル−4−イソチアゾリン
−3−オンと2−メチル−4−イソチアゾリン−
3−オンとの混合物0.01%、0.02%、また、それ
らの薬剤の併用例として、ヘキサヒドロ−1,
3,5−トリス(2−ヒドロキシエチル)−s−
トリアジン0.015%と1,2−ベンズイソチアゾ
ロン−3−オンの0.005%についても同様に試験
を行つた。 5-chloro-2-methyl-4-isothiazolin-3-one and 2-methyl-4-isothiazolin-
Mixtures with 3-one 0.01%, 0.02%, and examples of combinations of these drugs include hexahydro-1,
3,5-tris(2-hydroxyethyl)-s-
Similar tests were conducted with 0.015% triazine and 0.005% 1,2-benzisothiazolone-3-one.
比較例
対照としてサリチル酸を0.05%量添加したもの
を用いて試験を行つた。Comparative Example As a control, a test was conducted using a sample containing 0.05% salicylic acid.
第1図および第2図より本発明の防腐剤は、こ
れらを極微量添加することによつて、ポリマー泥
水の腐敗を抑え、粘度の低下を防止することがわ
かる。 From FIG. 1 and FIG. 2, it can be seen that the preservatives of the present invention, when added in extremely small amounts, can suppress spoilage of polymer slurry and prevent a decrease in viscosity.
第1図および第2図は本発明の実施例と比較例
により得られた結果を図表化したものである。第
1図の横軸は経過日数(日)を、縦軸は生菌数
(個/ml)を示し、第2図の横軸は経過日数
(日)を、縦軸は粘度(c.p.)を示す。
第1図中、
Γ−Γ:実施例1および2に記載された本発明
防腐剤を所定濃度添加した場合
●−●:0.05%サリチル酸添加の場合、および
●…●:無添加の場合を示す。
第2図では、
Γ−Γ:0.03%ヘキサヒドロ−1,3,5−ト
リス(2−ヒドロキシエチル)−s−ト
リアジン、
□−□:0.01%1,2−ベンズイソチアゾロン
−3−オン、
□…□:0.04%1,2−ベンズイソチアゾロン
−3−オン、
△−△:0.01%および0.02%の5−クロロ−2
−メチル−4−イソチアゾリン−3−オ
ンと2−メチル−4−イソチアゾリン−
3−オンとの混合物、
×−×:0.015%ヘキサヒドロ−1,3,5−
トリス(2−ヒドロキシエチル)−s−
トリアジンと0.005%1,2−ベンズイ
ソチアゾロン−3−オンとの混合物、お
よび
●−●:0.05%サリチル酸を添加した場合、な
らびに
●…●:無添加の場合を示す。
FIGS. 1 and 2 are graphical representations of the results obtained in Examples and Comparative Examples of the present invention. The horizontal axis in Figure 1 shows the number of days that have passed (days), the vertical axis shows the number of viable bacteria (cells/ml), and the horizontal axis in Figure 2 shows the number of days that have passed (days), and the vertical axis shows the viscosity (cp). show. In Figure 1, Γ-Γ: When the preservative of the present invention described in Examples 1 and 2 is added at a predetermined concentration; ●-●: When 0.05% salicylic acid is added; and ●...●: When no addition is made. . In Figure 2, Γ-Γ: 0.03% hexahydro-1,3,5-tris(2-hydroxyethyl)-s-triazine, □-□: 0.01% 1,2-benzisothiazolone-3-one, □... □: 0.04% 1,2-benzisothiazolone-3-one, △-△: 0.01% and 0.02% 5-chloro-2
-Methyl-4-isothiazolin-3-one and 2-methyl-4-isothiazoline-
Mixture with 3-one, ×−×: 0.015% hexahydro-1,3,5-
tris(2-hydroxyethyl)-s-
A mixture of triazine and 0.005% 1,2-benzisothiazolone-3-one, ●-●: the case where 0.05% salicylic acid was added, and ●...●: the case without addition.
Claims (1)
ドロキシエチル)−s−トリアジン、1,2−ベ
ンズイソチアゾロン−3−オン、および5−クロ
ロ−2−メチル−4−イソチアゾリン−3−オン
と2−メチル−4−イソチアゾリン−3−オンと
の混合物の1種以上を有効成分とすることを特徴
とする泥水工法用防腐剤。1 hexahydro-1,3,5-tris(2-hydroxyethyl)-s-triazine, 1,2-benzisothiazolone-3-one, and 5-chloro-2-methyl-4-isothiazolin-3-one and 2 - A preservative for muddy water construction, characterized in that the active ingredient is one or more of a mixture with methyl-4-isothiazolin-3-one.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13478079A JPS5657874A (en) | 1979-10-18 | 1979-10-18 | Antiseptic agent of mud drilling process |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13478079A JPS5657874A (en) | 1979-10-18 | 1979-10-18 | Antiseptic agent of mud drilling process |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5657874A JPS5657874A (en) | 1981-05-20 |
| JPS6238399B2 true JPS6238399B2 (en) | 1987-08-18 |
Family
ID=15136375
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13478079A Granted JPS5657874A (en) | 1979-10-18 | 1979-10-18 | Antiseptic agent of mud drilling process |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5657874A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61236885A (en) * | 1985-04-12 | 1986-10-22 | Terunaito:Kk | Muddy water material composition and its muddy water |
| JPH01152185A (en) * | 1987-12-08 | 1989-06-14 | Shimizu Corp | Mud water conditioner for civil engineering |
| AU2004201059B2 (en) * | 2003-03-26 | 2009-06-04 | Rohm And Haas Company | Microbicidal composition |
| CN112136820A (en) * | 2020-09-21 | 2020-12-29 | 西安三业新材料股份有限公司 | Reinforced metal working fluid anti-corrosion bactericide and preparation method and application thereof |
-
1979
- 1979-10-18 JP JP13478079A patent/JPS5657874A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5657874A (en) | 1981-05-20 |
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