TW575532B - Foundation solidifying materials - Google Patents

Foundation solidifying materials Download PDF

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Publication number
TW575532B
TW575532B TW87119051A TW87119051A TW575532B TW 575532 B TW575532 B TW 575532B TW 87119051 A TW87119051 A TW 87119051A TW 87119051 A TW87119051 A TW 87119051A TW 575532 B TW575532 B TW 575532B
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cement
english
chinese
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TW87119051A
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Chinese (zh)
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Motomu Miwa
Kenji Kayahara
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Kyokado Eng Co
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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K17/00—Soil-conditioning materials or soil-stabilising materials
    • C09K17/02—Soil-conditioning materials or soil-stabilising materials containing inorganic compounds only
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K17/00—Soil-conditioning materials or soil-stabilising materials
    • C09K17/02—Soil-conditioning materials or soil-stabilising materials containing inorganic compounds only
    • C09K17/04—Soil-conditioning materials or soil-stabilising materials containing inorganic compounds only applied in a physical form other than a solution or a grout, e.g. as granules or gases
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K17/00—Soil-conditioning materials or soil-stabilising materials
    • C09K17/02—Soil-conditioning materials or soil-stabilising materials containing inorganic compounds only
    • C09K17/10—Cements, e.g. Portland cement
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K17/00—Soil-conditioning materials or soil-stabilising materials
    • C09K17/02—Soil-conditioning materials or soil-stabilising materials containing inorganic compounds only
    • C09K17/12—Water-soluble silicates, e.g. waterglass
    • E—FIXED CONSTRUCTIONS
    • E02—HYDRAULIC ENGINEERING; FOUNDATIONS; SOIL SHIFTING
    • E02D—FOUNDATIONS; EXCAVATIONS; EMBANKMENTS; UNDERGROUND OR UNDERWATER STRUCTURES
    • E02D3/00—Improving or preserving soil or rock, e.g. preserving permafrost soil
    • E02D3/12—Consolidating by placing solidifying or pore-filling substances in the soil
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2103/00—Civil engineering use

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Soil Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Structural Engineering (AREA)
  • Agronomy & Crop Science (AREA)
  • Environmental & Geological Engineering (AREA)
  • Mining & Mineral Resources (AREA)
  • Paleontology (AREA)
  • Civil Engineering (AREA)
  • General Engineering & Computer Science (AREA)
  • Soil Conditioners And Soil-Stabilizing Materials (AREA)
  • Consolidation Of Soil By Introduction Of Solidifying Substances Into Soil (AREA)

Description

575532 五、發明說明(1) 本發明係關於中性矽溶膠、微粒水泥系之懸濁型地盤 固結材,尤指一種滲透時間可增長、滲透性優異、且具有 高固結強度之地盤固結材。 做為固結地盤之地盤注入用膠結材方面,以往已有種 種之揭示者,例如,使用莫耳比小、驗度高之水玻璃之、熔 渣系水玻璃膠結材即為其一,該膠結材雖具有高固結強 度,但有鹼份溶出之問題。再者,習知有將多價金屬添加 於中性矽溶膠内而為地盤膠結材者,唯其固結強度低,是 為其缺點。為了改良該固結強度,近年來係採用一種將中 性矽溶膠與波特蘭水泥以1 . 5的比例而予以合流注入之方 法,然而,該合流注入之膠結材之膠化時間最多只在一分 鐘以内,其膠化時間甚短暫,致使滲透性亦差。 另外,習知亦有將高爐熔渣粉末及波特蘭水泥添加於 中性矽溶膠内而為膠結材者,但於其使用具有中性矽溶膠 之膠結材時,一般在地上藉由量杯倒立法測得之膠化時間 甚短,且於土中之膠化時間係更加短暫,因而滲透性差, 且容易於土粒之間產生堵塞現象,而有於土中不能增長膠 化時間之缺點。 本發明旨在解決上述習知例之缺點,而研發一種新穎 技術之地盤固結材,係將特定量之中性矽溶膠及微粒水泥 及視需要而定之微粒熔渣等於一定之條件下予以配合,該 配合液係呈現漸漸增黏及其次為保持可塑狀態之明確之膠 化時間。此種狀態之配合液係有良好滲透性,又可容易調 整增黏時間,遂能增長滲透時間,且當注入完畢之後,係575532 5. Description of the invention (1) The present invention relates to a suspension type site consolidation material of neutral silica sol and fine particle cement system, especially a site consolidation which can increase the penetration time, has excellent permeability, and has high consolidation strength. Results. As cementing materials for site injection of consolidated sites, there have been various disclosures in the past. For example, the use of water glass with a small mole ratio and a high degree of inspection, and slag-based water glass cement is one of them. Although the cementing material has high consolidation strength, it has the problem of alkali dissolution. Furthermore, it is known that those who add polyvalent metals to the neutral silica sol to make cementitious materials on the site, but its low consolidation strength is its disadvantage. In order to improve the consolidation strength, a method of injecting neutral silica sol and Portland cement at a ratio of 1.5 in recent years has been adopted. However, the gelation time of the cemented material injected by this confluence is only at most Within one minute, its gelation time is very short, resulting in poor permeability. In addition, it is also known to add blast furnace slag powder and Portland cement to the neutral silica sol as a cementing material. However, when using a cementing material with a neutral silica sol, it is generally poured on the ground with a measuring cup. The gelation time measured by legislation is very short, and the gelation time in the soil is shorter, so the permeability is poor, and it is easy to cause clogging between soil particles, and it has the disadvantage that the gelation time cannot be increased in the soil. The present invention aims to solve the shortcomings of the above-mentioned conventional examples, and develops a novel technology for site consolidation materials, which is a combination of a specific amount of neutral silica sol and particulate cement and particulate slag as required under certain conditions. The compounding liquid system gradually exhibits a definite viscosity and a clear gelation time for maintaining a plastic state. The blending liquid system in this state has good permeability, and it is easy to adjust the viscosity increasing time, which can increase the penetration time.

575532 五、發明說明(2) 失去流動性而實質地固結,而與呈現膠化時間之膠結材具 有相同之功效。 本發明旨在提供一種參透時間增長、滲透性優異、固 結強度高及鹼份溶出甚少而不會影響環境之中性矽溶膠、 微粒水泥系之懸濁型地盤固結材, 為達成上述目的,本發明之地盤固結材係藉由離子交換樹 脂處理水玻璃,而將水玻璃中之大部份鹼份予以除去,再 經由造粒而得中性矽溶膠,並將此中性矽溶膠及微粒水泥 及視需要而定之微粒熔渣等做為有效成份而予以配合,上 述中性矽溶膠之配合量係為於配合之後,使增黏不致形成 為明顯膠化狀態之量,而以具有以下要件(1 )及(2 )之任一 者或兩者為本發明之特徵。即: (1 )以靜置配合液而使粒子沉降後之不含粒子之液體量對 全體配合液之比率,即,沉降率係成為4 0 %以下者。 (2 )於經過1分鐘以上之配合後之配合液係呈可塑狀態,且 可持續1 0分鐘以上之可塑狀態者。 以下就本發明之地盤固結材具體詳述之。 按本發明之地盤固結材係於配合之後即行增黏,不久 之後黏度增高而保持可塑狀態,但不會產生膠化現象,其 增黏時間為1分鐘以上,而以約1 0〜1 2 0分鐘為妥適,且隨 後持續保持2 0分鐘為佳。 再者,按本發明之地盤固結材係以沉降率,即,以靜 置配合液而使粒子沉降後之不含粒子之液體量對全體配合 液之比率係藉由增黏而成為4 0 %以下之配合。尚且,於增575532 V. Description of the invention (2) It loses its fluidity and solidifies substantially, and has the same effect as the cementitious material showing the gelation time. The present invention aims to provide a suspension type site consolidation material with a long penetration time, excellent permeability, high consolidation strength, and little alkali dissolution without affecting the environment, such as neutral silica sol and particulate cement. Purpose, the site consolidation material of the present invention is to treat water glass by ion exchange resin, to remove most of the alkali in the water glass, and then to obtain a neutral silica sol through granulation, and the neutral silica Sol and particulate cement and particulate slag as required are added as effective ingredients. The above-mentioned neutral silica sol is blended in such a way that the thickening does not form a significant gelation state after blending. Either or both of the following requirements (1) and (2) are features of the present invention. That is: (1) The ratio of the amount of the liquid containing no particles after the particles are settled to the total amount of the compounded liquid, that is, the sedimentation rate is 40% or less. (2) The compounding liquid system after being mixed for more than 1 minute is in a plastic state, and it can be in a plastic state for more than 10 minutes. The site consolidation material of the present invention will be described in detail below. The consolidation material of the construction site according to the present invention is thickened after being compounded, and the viscosity is increased after a while to maintain the plasticity state, but no gelation will occur. Its thickening time is more than 1 minute, and about 10 to 12 0 minutes is appropriate, and then it is better to continue for 20 minutes. In addition, the site consolidation material according to the present invention uses the sedimentation rate, that is, the ratio of the amount of the liquid containing no particles after the particles are settled to the total solution, after the particles are settled by standing the solution. % Below match. Also, Yu Zeng

575532 五、發明說明(3) 黏之後,為使其不會形成可塑狀態,則沉降率以2 0 %以下 為佳。 本發明地盤固結材係以具有於配合後經過1分鐘以 上’再使可塑狀態持續保持1 0分鐘以上之條件,及使配合 液之沉降率為4 0 %以下之條件中之任一者或兩者為其特 徵。 按上述本發明之配合液注入地盤時,在地盤為緊密之 場合,配合液係於增黏階段以習知膠化之相同時間進行作 用而不能滲透。另於地盤為粗質之場合,配合液係可從增 黏階段以可塑狀態持續注入(滲透)。 再者,本發明係預先將瞬結膠結劑注入地盤中而行粗 塞之後,再將本發明之地盤固結材作為緩結膠結劑而注入 地盤中,遂能進一步增進地盤之改良效果。 此處,習知地盤固結材係以量杯倒立法測定膠化時 間,對於其以量杯倒立而地盤固結材不流出之時間做為膠 化時間之情形而言,本發明則係以B型黏度計測定膠化時 間,而對於大約為500 cps(centipoise)以上至1000 cps 以下之地盤固結材者,即使以量杯倒立法予以測定時,亦 不會有無法自量杯流出之情形,是以,使用B型黏度計測 定膠化時間時,係以自調配其配合液時至黏度為5 0 0 c p s 為止之過程時間作為其「增黏時間」。尚且,若以B型黏 度計測定懸濁液則有若干問題,但習知膠化型地盤固結材 若以B型黏度計測定其配合液之黏度的話,在增黏一旦開 始時,其黏度即急劇上升膠化而成為2 0 0 0 c p s以上之高黏575532 5. Description of the invention (3) After sticking, in order to prevent it from forming a plastic state, the sedimentation rate is preferably less than 20%. The consolidation material for the construction site of the present invention is any one of a condition that the plasticized state is continuously maintained for more than 10 minutes after more than 1 minute has elapsed after the compounding, and that the sedimentation rate of the compounding liquid is 40% or less. Both are characteristic. When the compound liquid according to the present invention is injected into the site, when the site is compact, the compound liquid acts in the thickening stage at the same time as conventional gelation and cannot penetrate. On the other hand, when the site is coarse, the compounding liquid system can be continuously injected (infiltrated) in a plastic state from the thickening stage. Furthermore, after the instant cement is injected into the site in advance for rough plugging, the site consolidation material of the present invention is injected into the site as a retarding cement, which can further improve the improvement effect of the site. Here, the conventional site consolidation material uses a measuring cup to invert legislation to measure the gelation time. For the case where the measuring cup is inverted and the site consolidation material does not flow out as the gelation time, the present invention uses a type B The viscometer measures the gelation time, and for those solidified materials on the site of about 500 cps (centipoise) to less than 1000 cps, even if it is measured with a measuring cup inverted legislation, there will be no situation where it cannot flow out of the measuring cup. When using a B-type viscometer to measure the gelation time, the process time from the time when the compound solution is prepared to the viscosity of 500 cps is used as its "thickening time". Moreover, there are some problems if the suspension is measured with a B-type viscometer, but it is known that if the viscosity of the compounding liquid is measured with a B-type viscometer, the viscosity of the compounding liquid will be at the beginning of thickening. That is, it sharply rises to gel and become highly viscous above 2000 cps.

575532 五、發明說明(4) 度,因而將以B型黏度計測定之值作為一個大約的標準。 上述之膠化係謂液狀之配合液因藉化學反應而具有保 形性,而在如上所述之以量杯倒立法予以測定時,係呈即 使將量杯輕斜也流不出之狀態。此種配合液一旦膠化時即 呈完全不會滲透,而迥異於本發明之能保持可塑狀態之配 合液。再者,即使以量杯倒立法將未膠化之配合液注入地 盤後,在土粒子間若未被施加外力即會漸行固化(或固 結),這種性質亦不相當於本發明之「未形成明顯之膠化 狀態」。尚且,本發明之增黏時間為1 0分鐘以上之配合 者,則幾乎可持續維持1 0分鐘以上之可塑狀態。 再者,沉降率係上述配合液之幾約全體固結之一個標 準。在使用B型黏度計測定其黏度為5 0 0 c p s以上之場合, 其沉降率幾乎皆為4 0 %以下,由於一般場合之沉降率皆為 數個百分比以下之故,黏度是否為5 0 0 c p s便成為一個判 定基準。 由於未膠化之配合液通常有或多或少之沉降,尤其是 低黏度之配合液之沉降率則較大,但當配合液成為可塑狀 態時,實質上粒子幾乎不會沉降。沉降率係例如將配合液 置於量筒等内且予以靜置,而藉由靜置後所分離出之水量 以算出沉降率。再者,在配合液注入完畢後之已不流動之 階段時,因其沉降率係關係到固結物之均一性、止水性及 強度等,是以,本發明則係測定配合液之於增黏後之沉降 率 〇 再者,可塑狀態係謂當藉注入等外力之施加時呈現流575532 5. Description of the invention (4) degrees, so the value measured by the B-type viscometer is used as an approximate standard. The above-mentioned gelation means that the liquid compounding liquid has shape retention due to a chemical reaction, and when it is measured by the measuring cup inversion method as described above, it is in a state that the measuring cup cannot be flowed out even if it is tilted slightly. Such a compounding liquid is completely impermeable once gelatinized, which is quite different from the compounding liquid of the present invention which can maintain a plastic state. Furthermore, even if the ungelatinized compound solution is injected into the site with the measuring cup inverted legislation, it will gradually solidify (or consolidate) if no external force is applied between the soil particles. This property does not correspond to the " No obvious gelatinous state was formed. " Moreover, if the viscosity-increasing time of the present invention is more than 10 minutes, a plastic state of more than 10 minutes can be almost continuously maintained. In addition, the sedimentation rate is a standard for the consolidation of the whole of the above-mentioned complex liquid. When using a B-type viscometer to measure the viscosity of more than 500 cps, the sedimentation rate is almost 40% or less. Since the sedimentation rate of general occasions is less than a few percentages, is the viscosity 5500 cps? It becomes a judgment criterion. Since the ungelatinized complexing liquid usually has more or less sedimentation, especially the low viscosity complexing liquid has a larger sedimentation rate, but when the complexing liquid becomes a plastic state, the particles hardly settle. The sedimentation rate is, for example, that the compounding liquid is placed in a graduated cylinder or the like and allowed to stand still, and the sedimentation rate is calculated from the amount of water separated after standing. Furthermore, at the stage where the compound solution is not flowing after the injection is completed, the sedimentation rate is related to the uniformity, water resistance and strength of the solidified substance. Therefore, the present invention measures the increase of the compound solution. Settling rate after sticking. Furthermore, the plasticity state means that when an external force such as injection is applied, it shows a flow.

575532 五、發明說明(5) 動性,但一旦除去外力時則呈現不流動性之狀態。在配合 之際,當形成此種可塑狀態時,則滲透性會變差之故,本 發明則無此種情形,即本發明必須至少經過1分鐘以上才 形成可塑狀態。又,在可塑狀態之持續時間短的場合,隨 後之膠化情形亦有可能產生,因此,可塑狀態時間必須至 少持續1 0分鐘以上,而以持續6 0分鐘以上為佳。隨後,即 使藉由靜置等而行固化亦不會影響本發明之目的之達成。 上述本發明係以中性矽溶膠、微粒水泥、最好為併用 微粒熔渣之微粒水泥做為主成份之地盤固結材,中性矽溶 膠之使用量係為使配合液增黏之必要量,即,使用量係為 配合液全體之0 . 5〜4 % (容量)之量,微粒水泥係為布倫比 表面積4 0 0 0 c m V g以上者,亦可視需要而添加增黏時間之 調整劑。 尚且,以離子交換樹脂將水玻璃施行脫鹼而得之活性 二氧化矽,因係僅與碳酸氫鈉混合之後即可行膠化,是 以,在膠化之前,即使將上述使用量之活性二氧化矽與水 泥懸濁液混合時,亦不會產生如使用本發明之活性二氧化 矽之情形一般之可塑狀態。 按本發明之地盤固結材,上述中性矽溶膠之配合量係 為配合液於增黏時,不會產生有如水玻璃溶液型膠結劑之 均勻凝膠般彈性力之凝膠之量,該配合量復因微粒水泥之 粒度與微粒熔渣之併用,甚至因增黏時間之調整劑之添加 量而有所不同。 在可行滲透之時間方面,因地盤之狀況而顯然有所不575532 V. Description of the invention (5) Mobility, but once the external force is removed, it will appear immobile. At the time of cooperation, when such a plastic state is formed, the permeability will be deteriorated, but the present invention does not have such a case, that is, the invention must take at least 1 minute to form a plastic state. In addition, in the case where the duration of the plastic state is short, subsequent gelatinization may occur. Therefore, the time of the plastic state must be at least 10 minutes, and preferably 60 minutes or more. Subsequently, even if curing is performed by standing or the like, the achievement of the object of the present invention is not affected. The above-mentioned invention is a site consolidation material comprising neutral silica sol, fine particle cement, preferably fine particle cement in combination with fine slag, and the use amount of the neutral silica sol is necessary for thickening the compound liquid. That is, the amount used is 0.5 ~ 4% (capacity) of the whole compound solution, and the fine particle cement is the one with a Brun specific surface area of more than 4 00 cm V g, and an adjustment of the thickening time can be added as needed. Agent. Moreover, the active silica obtained by de-alkalizing water glass with ion exchange resin can be gelled only after mixing with sodium bicarbonate. Therefore, even before the gelation, When the silica is mixed with the cement suspension, it does not produce a plastic state like that in the case of using the active silica of the present invention. According to the site consolidation material of the present invention, the blending amount of the above-mentioned neutral silica sol is the amount of the gel that does not produce an elastic force like the uniform gel of a water glass solution type cement when the blending solution is thickened. The compounding amount is different due to the combination of the particle size of the particulate cement and the particulate slag, and even the amount of the adjusting agent for the thickening time. In terms of the time of feasible penetration, it is obviously different due to the condition of the site

第10頁 575532 五、發明說明(6) 同乃自不待言,在使用一般的中性矽溶膠之習知矽溶膠 -水泥系膠結劑時,其膠化時間約3 0分鐘以内(尤其是夏天 約為3分鐘以内,而幾乎不可能增長膠化時間),不僅膠 化時間極短,尚且,增黏開始後之膠化係急激地產生,又 於膠化後之凝膠強度亦非常大,遂不能破壞凝膠以行滲 透,此係習知例之缺點。Page 10 575532 V. Description of the invention (6) It is self-evident that when using the conventional silica sol-cement cement as a general neutral silica sol, its gelation time is within 30 minutes (especially in summer) Within about 3 minutes, it is almost impossible to increase the gelation time). Not only the gelation time is extremely short, but also the gelation system after the thickening begins to occur sharply, and the gel strength after gelation is also very large. It is not possible to break the gel for penetration, which is a disadvantage of the conventional example.

鑑於該習知例之缺點,本發明之地盤固結材則係可使 增黏時間增加至1小時以上,尚且所謂之凝膠強度(本發 明因係形成可塑狀態,而不稱為凝膠強度)亦弱,而於增 黏時間經過之後亦能滲透地盤,如此,遂能充分延長可行 渗透之時間。 再者,對於將水泥以單獨之懸濁液注入地盤之情形而 言,水泥係一邊堵塞孔隙一邊下降,唯本發明之地盤固結 材則係能以中性矽溶膠中之二氧化矽附著於水泥粒子上, 使得水泥粒子間之潤滑性良好之故,遂使滲透性亦佳,再 藉由其後之增黏而可使幾乎全部之注入液形成固化。In view of the shortcomings of this conventional example, the site consolidation material of the present invention can increase the thickening time to more than 1 hour, and the so-called gel strength (the present invention is not plastic strength because it forms a plastic state) ) Is also weak, and can penetrate the site after the thickening time has elapsed. In this way, the time of feasible penetration can be fully extended. Furthermore, for the case where cement is injected into the site with a separate suspension liquid, the cement system descends while blocking the pores, but the site consolidation material of the present invention can be attached to the silica with a neutral silica sol. On the cement particles, the lubricity between the cement particles is good, so the permeability is also good, and then by the subsequent thickening, almost all of the injection liquid can be solidified.

本發明使用之中性矽溶膠係將水玻璃施以離子交換樹 脂處理而分離除去幾約全部之N a離子等之鹼,且經加熱造 粒得到粒徑6〜5 0毫微米之半透明液體,且為中性〜弱 鹼性,最好為P Η值8 . 0〜1 0 . 5之弱鹼性、比重為1 . 1 6〜 1. 24、Si 0飪10〜4 0 %重量、及“2〇為0· 0 1〜4 %重量等範圍 内者。 當N a 20為4 W %以上時,矽酸膠體即行溶解,而形成矽 酸鹽之水溶液。另一方面,當Na 20為0 . 0 1 W%以下時,矽酸The present invention uses a neutral silica sol to treat water glass with an ion exchange resin to separate and remove almost all alkalis such as Na ions, and to obtain a translucent liquid with a particle size of 6 to 50 nm by heating and granulation. And is neutral to weakly alkaline, preferably a weak alkaline with a P value of 8. 0 to 1 0.5, a specific gravity of 1. 16 to 1. 24, Si 0 to 10 to 40% by weight, And "2〇 is in the range of 0 · 0 1 ~ 4% by weight. When Na 20 is 4 W% or more, the silicic acid colloid is dissolved and an aqueous solution of silicate is formed. On the other hand, when Na 20 When it is below 0.1 W%, silicic acid

第11頁 575532 五、發明說明(7) 膠體係安定存在而行凝集者。即,N a 20在0 . 0 1〜4 %重量範 圍内時,N a離子係可分佈於矽酸膠體之表面,而保持安定 之膠體狀。在此情形,矽酸膠體之粒徑係大約以6〜5 0毫 微米為主。又當矽酸膠體之粒徑大於5 0毫微米時則行沉 澱。 上述之矽酸膠體係以莫耳比(S i 0 2 / N a 20)約為1 0 0 0 〜1 0、P Η值為8〜1 0,而利於膠體之安定。如此調製之矽 酸膠體係形成半永久性之安定,因此,在其自工廠運到工 地或行注入之際,將無膠化之慮。 本發明使用之微粒水泥自滲透性方面觀之,係以布倫 比表面積4000 cm2/ g以上者為佳。欲使增黏時間更加延長 時,尤其要增加微粒水泥之量。再者,在容易膠化之配合 之場合,若欲獲得不易膠化之配合,則可藉由併用微粒熔 渣而達成。併用之微粒熔渣之布倫比表面積係為4 0 0 0 cm V g 以上,且以10000 cm2/ g以上者為佳。 固結物之強度係可依用途而適當選擇,唯微粒水泥之 使用量係以地盤固結材1 0 0 0 0 m 1對3 0〜5 0 0 g之比例者為 佳。尤其,為了要獲得高強度、耐久性之固結物時,則微 粒水泥之使用量係以地盤固結材1 0 0 0 0 m 1對5 0 g以上者為 佳,甚至,若併用微粒熔渣亦甚佳。在此場合,微粒水泥 與微粒熔渣之比例係以8 0〜2 0 : 2 0〜8 0為佳。 按上述本發明之中性矽溶膠一微粒水泥系方面,係可 藉由改變中性矽溶膠及微粒水泥之使用量而行調整增黏時 間,但若進一步藉由添加增黏時間用之調整劑而延遲增黏Page 11 575532 V. Description of the invention (7) Those who have a stable glue system and perform agglutination. That is, when Na 20 is in the range of 0.01 to 4% by weight, Na ion can be distributed on the surface of the silicic acid colloid while maintaining a stable colloidal shape. In this case, the particle size of the silicic acid colloid is mainly about 6 to 50 nm. When the particle size of the silicic acid colloid is greater than 50 nm, precipitation occurs. The above-mentioned silica gel system has a molar ratio (S i 0 2 / Na 20) of about 1 0 0 to 1 0, and a P value of 8 to 10, which is beneficial to the stability of the colloid. The thus prepared silicic acid glue system forms a semi-permanent stability, so when it is transported from the factory to the construction site or injected, there is no concern about gelation. In terms of the self-permeability of the particulate cement used in the present invention, it is preferable that the specific surface area of the buren is 4000 cm2 / g or more. In order to make the thickening time longer, especially increase the amount of particulate cement. Furthermore, in the case of a compound that is easy to gel, if it is desired to obtain a compound that is not easy to gel, it can be achieved by using particulate slag in combination. The combined surface area of the particulate slag used in combination is 4,000 cm V g or more, and preferably 10,000 cm2 / g or more. The strength of the consolidated material can be appropriately selected according to the application, but the amount of particulate cement used is preferably a ratio of 1 000 0 0 m 1 to 3 0 to 5 0 g of the site consolidation material. In particular, in order to obtain a high-strength, durable consolidation, the amount of particulate cement used is preferably the site consolidation material 1 0 0 0 0 m 1 to 50 g or more. The slag is also very good. In this case, the ratio of the particulate cement to the particulate slag is preferably 80 to 20:20 to 80. According to the above aspect of the neutral silica sol-fine cement system of the present invention, the thickening time can be adjusted by changing the use amount of the neutral silica sol and fine particle cement, but if further adjusting agent for thickening time is added Delayed thickening

第12頁 575532 五 、發明說明 (8) 時 間 之 際 則 因 低 黏 度 化 而 可 增 進 滲 透 性 〇 在 欲 以 短 時 間 行 膠 化 之 場 合 可 藉 由 添 加 增 黏 時 間 用 之 調 整 劑 而 達 成 且 增 黏 時 亦 不 產 生 膠 化 〇 增 黏 時 間 之 調 整 劑 之 使 用 量 係 依 地 盤 注 入 材 之 使 用 條 件 尤 其 J 可 依 液 溫 而 適 當 選 擇 但 能 使 增 黏 時 間 為 3 0分 鐘 以 上 甚 至 視 需 要 而 調 整 為 數 小 時 以 上 係 本 發 明 之 特 徵 在 此 情 形 下 增 黏 時 間 之 調 整 劑 量 係 可 使 用 對 微 粒 水 泥 0· 1、 -1 .0 %重量者^ 上 述 增 黏 時 間 之 調 整 劑 係 可 為 如 驗 金 屬 之 碳 酸 氫 鹽 Λ 碳 酸 鹽 、 填 酸 鹽 酸 性 石粦 酸 鹽 Λ 焦 磷 酸 鹽 Λ 檸 檬 酸 Λ 酒 石 酸 5 木 質 石黃 酸 鈉 聚 石黃 酸 納 等 之 ( 延 遲 性 ) 水 泥 流 動 劑 等 Ο 上 述 調 整 劑 之 中 , 尤 以 對 固 定 物 之 強 度 影 響 少 之 驗 金 屬 之 碳 酸 氫 鹽 及 碳 酸 鹽 做 為 T^7 取 佳 之 調 整 劑 〇 此 種 增 黏 時 間 之 調 整 劑 係 添 加 至 中 性 矽 溶 膠 側 而 在 注 入 時 與 微 粒 水 泥 之 懸 濁 液 混 合 之 效 果 較 良 好 〇 再 者 在 添 加 水 泥 流 動 劑 之 場 合 係 以 添 加 至 微 粒 水 泥 側 為 佳 在 此 場 合 其 他 之 調 整 劑 則 係 添 加 至 中 性 矽 溶 膠 側 為 佳 〇 在 添 加 調 整 劑 之 場 合 係 預 先 使 其 溶 解 於 水 中 之 後 再 行 添 加 中 性 矽 溶 膠 之 方 法 為 佳 又 曰 取 好 選 擇 使 用 狀 態 均 一 之 調 整 劑 〇 尚 且 , 由 於 添 加 增 黏 時 間 之 調 整 劑 遂 能 使 A B兩 液 混 合 時 之 黏 度 變 小 而 使 渗 透 性 更 進 一 步 增 高 〇 以 下 就 本 發 明 之 實 施 例 具 體 詳 述 之 〇 此 等 實 施 例 僅 為Page 12 575532 V. Description of the invention (8) In the case of time, the permeability can be improved due to low viscosity. In the case of gelling in a short time, it can be achieved and increased by adding an adjusting agent for thickening time. There is no gelation when sticking. The amount of the adjusting agent for the thickening time depends on the use conditions of the injection material on the site. Especially J can be appropriately selected according to the liquid temperature, but the thickening time can be more than 30 minutes or even adjusted as needed. It is a feature of the present invention for several hours or more. In this case, the adjusting amount of the thickening time can be used for the fine cement of 0.1, -1. 0% by weight. Bicarbonate Λ Carbonate, Filler Acidic Carboxylate Λ Pyrophosphate citrate citrate tartaric acid 5 Sodium lignin lutein sodium polysulfonate etc. ) Cement flow agent, etc. Among the above-mentioned adjusting agents, especially bicarbonate and carbonate salts of metal test, which have little effect on the strength of the fixture, are the best adjusting agents for T ^ 7. This type of adjusting agent for thickening time The effect of adding to the neutral silica sol side and mixing with the suspension of particulate cement during injection is better. Furthermore, in the case of adding cement flow agent, it is better to add to the particulate cement side. In this case, other adjusting agents It is better to add it to the side of the neutral silica sol. In the case of adding an adjusting agent, it is better to dissolve it in water before adding the neutral silica sol. It is better to choose an adjusting agent with a uniform use state. The addition of the viscosity increasing time adjusting agent can make the viscosity of the two AB liquids smaller and make the permeability even higher. In the following the present invention will of Example described later in detail with the square body like this is only of Example

第13頁 575532 五、發明說明(9) 本發明所舉之例,本發明並未限定為此等實施例所舉例 者,凡本發明精神所涵蓋者皆屬本發明申請專利範圍,而 自不待言。 本發明之實施例及比較例使用之中性矽溶膠、熔渣、 水泥及增黏時間之調整劑内容係彙整表示如下。 (1 )中性矽溶膠: 使用將水玻璃施以離子交換樹脂處理以除去大部份之 鹼之後經造粒而獲得之如表1所示成份之旭電化工業 (株)製之中性矽溶膠。Page 13 575532 V. Description of the invention (9) The examples of the present invention are not limited to those exemplified in these embodiments, and those covered by the spirit of the present invention belong to the scope of patent application of the present invention, and are not to be waited for. Speak. The contents of the modifiers used in the examples and comparative examples of the present invention, such as neutral silica sol, slag, cement, and tackifier time, are collectively shown below. (1) Neutral silica sol: The neutral silica produced by Asahi Denka Kogyo Co., Ltd. with the composition shown in Table 1 is obtained by subjecting water glass to ion exchange resin treatment to remove most of the alkali, followed by granulation. Sol.

【表1】 比重 Si02 (%) PH 粒徑 (毫微米 millimicron) 1.20 30.5 9.5 10 〜20 (2 )熔渣: 使用如表2所示成份及粉碎度各不相同之三種熔渣。 【表2】 熔渣 Si〇2 ai2〇3 Fe2〇3 CA〇 MGO 鹽基度 水硬率 布倫比表 之種類 (%) (%) (%) (%) (%) 面積cm2/g 1 31.4 18.6 ' 1.0 46.2 1.3 2.11 .0.91 8.000 2 31.4 18.6 1.0 46.2 1.3 2.11 .0.91 10.000 j 31.4 18.6 1.0 46.2 1.3 2.11 .0.91 15.000[Table 1] Specific gravity Si02 (%) PH particle size (millimicron) 1.20 30.5 9.5 10 ~ 20 (2) Slag: Use three types of slag with different composition and grind degree as shown in Table 2. [Table 2] Types of slag Si〇2 ai2〇3 Fe2〇3 CA〇MGO Salinity and hydraulicity Bronby table (%) (%) (%) (%) (%) Area cm2 / g 1 31.4 18.6 '1.0 46.2 1.3 2.11 .0.91 8.000 2 31.4 18.6 1.0 46.2 1.3 2.11 .0.91 10.000 j 31.4 18.6 1.0 46.2 1.3 2.11 .0.91 15.000

(3 )水泥:(3) Cement:

第14頁 575532 五、發明說明(ίο) 使用如表3所示成份及粉碎度各不相同之波特蘭水泥及 南爐水泥。 【表3】 水泥 之種類 Si02 (%) Al2〇3 (%) Fe203 (%) CA〇 (%) MG〇 (%) 鹽基度 水硬率 布倫比表 面積cm:/’g 波特蘭水泥 21.9 5.3 3.1 65.1 1.4 3.28 2.15 3200 波特蘭水泥 21.9 5.3 3.1 65.1 1.4 3.28 2.15 6200 波特蘭水泥 21.9 5.3 3.1 65.1 1.4 3.28 2.15 8100 波特蘭水泥 21.9 5.3 3.1 65.1 1.4 3.28 2.15 10000 高爐水泥 25.8 9.4 2.0 54.9 3.4 2.61 1.47 8300 高爐水 25.8 9.4 2.0 54.9 3.4 2.61 1.47 9700 (4 )增黏時間之調整劑: 使用增黏時間之調整劑之具代表性之碳酸氫鈉(試劑 一級:NaHCOa)。 實施例1〜9及比較例1〜6 : 表1之中性矽溶膠及碳酸氫鈉係做為A液,而B液則 使用熔渣及水泥之懸濁液,將A液與B液依表4之比例予 以混合,而調製成各種之地盤固結材。已製成之地盤固結 材係藉B型黏度計測定增黏時間,復依照日本土質工學會 基準「土之一軸壓縮試驗方法」而測定一軸壓縮強度。實 施例1〜9之任一配合,皆係增黏後持續1 〇分鐘以上之可塑 狀態,其結果乃如表4所示。 【表4】Page 14 575532 V. Description of the invention (ίο) Use Portland cement and South furnace cement with different composition and grind degree as shown in Table 3. [Table 3] Types of cement Si02 (%) Al2〇3 (%) Fe203 (%) CA〇 (%) MG〇 (%) Salinity hydraulic specificity Braun specific surface area cm: / 'g Portland cement 21.9 5.3 3.1 65.1 1.4 3.28 2.15 3200 Portland cement 21.9 5.3 3.1 65.1 1.4 3.28 2.15 6200 Portland cement 21.9 5.3 3.1 65.1 1.4 3.28 2.15 8100 Portland cement 21.9 5.3 3.1 65.1 1.4 3.28 2.15 10000 Blast furnace cement 25.8 9.4 2.0 54.9 3.4 2.61 1.47 8300 Blast furnace water 25.8 9.4 2.0 54.9 3.4 2.61 1.47 9700 (4) Adjusting agent for thickening time: A representative sodium bicarbonate (reagent level: NaHCOa) is used for adjusting the thickening time. Examples 1 to 9 and Comparative Examples 1 to 6: In Table 1, the neutral silica sol and sodium bicarbonate are used as the A liquid, and the B liquid is a suspension liquid of slag and cement. The ratios in Table 4 were mixed to prepare various site consolidation materials. The completed site consolidation material was measured by a B-type viscometer to measure the thickening time, and the uniaxial compressive strength was measured in accordance with the Japanese Geotechnical Society's standard "One Soil Axial Compression Test Method". Any combination of Examples 1 to 9 is a plastic state that lasts for more than 10 minutes after thickening. The results are shown in Table 4. 【Table 4】

第15頁 575532 五、發明說明(11) 實施例 Α液(500ml) B液(500mJ) A B合流液 比較例 中性 碳酸氫鈉 水 熔渣 水泥水 增黏 —軸壓縮強度 矽溶膠 (g) 時間 (Kg / cm2) NO. (g) (ml) 表2 重量 表2 重量 水 (分) 7曰 30曰 之N, (g) 之N (g) (ml) 實一1 30 5 殘餘 j 150 4 50 殘餘 60 14.9 33.0 實一2 60 5 殘餘 3 150 4 50 殘餘 40 16.3 41.5 實一 3 15 2.5 殘餘 3 150 4 50 殘餘 80 12.5 30.1 實一4 15 5 殘餘 2 150 4 50 殘餘 70 11.8 29.6 银 Γ 貝一〇 30 6 殘餘 6 200 殘餘 30 9.6 25.7 宙 a Μ一〇 60 3 殘餘 1 150 4 50 殘餘 60 10.5 35.9 «k? η 貝一/ 15 2.5 殘餘 1 150 j 50 殘餘 110 9.1 27.6 實一8 60 2 殘餘 4 200 殘餘 20 17.2 39.4 實一9 60 勹 J 殘餘 ? 200 殘餘 40 8.9 30.2 比一1 240 16 殘餘 3 150 4 50 殘餘 膠化 18.8 44.1 比一2 180 7.5 殘餘 3 150 4 50 殘餘 膠化 17.0 42.4 比一3. 180 10 、殘餘 3 150 丨 5 50 殘餘 膠化 12.4 33.9 比一4 殘餘 勹 j 150 5 50 殘餘 注1 5.3 14.4 比一5 240 16 殘餘 4 200 殘餘 膠化 22.3 40.2 比一6 60 5 殘餘 勹 j 150 1 1 50 殘餘 注2 3.7 10.3Page 15 575532 V. Description of the invention (11) Example A liquid (500ml) B liquid (500mJ) AB combined liquid Comparative example neutral sodium bicarbonate water slag cement water thickening-axial compressive strength silica sol (g) time (Kg / cm2) NO. (G) (ml) Table 2 Weight Table 2 Weight Water (Min) 7-30 N, (g) N (g) (ml) Real 1 30 5 Residual j 150 4 50 residual 60 14.9 33.0 solid 2 60 5 residual 3 150 4 50 residual 40 16.3 41.5 solid 3 15 2.5 residual 3 150 4 50 residual 80 12.5 30.1 solid 4 15 5 residual 2 150 4 50 residual 70 11.8 29.6 silver 1030 6 Remaining 6 200 Remaining 30 9.6 25.7 Zea M 1 0 60 3 Remaining 1 150 4 50 Residual 60 10.5 35.9 «k? Η Bayi / 15 2.5 Remaining 1 150 j 50 Remaining 110 9.1 27.6 Real 8 8 2 Residual 4 200 Residual 20 17.2 39.4 Real 9 60 勹 J Residual? 200 Residual 40 8.9 30.2 Ratio 1 240 16 Residual 3 150 4 50 Residual Gelation 18.8 44.1 Residual 2 180 7.5 Residual 3 150 4 50 Residual Gelation 17.0 42.4 Than 3. 180 10, Residual 3 150 丨 5 50 Residual gelation 12.4 33.9 Than 4 Residual j 150 5 50 1 5.3 14.4 Note residue residue residue gelled than 4200 524 016 22.3 40.2 a ratio of a residue Bao 6605 j 150 1 1 50 2 3.7 Residual 10.3 NOTE

注1 :經過3小時後幾乎全部未增黏。Note 1: After 3 hours, almost no viscosity increase.

注2 ··經過3小時後亦未達到5 0 0 CPS增黏。 增黏時間係於液溫2 0 0 C進行測定者。 以下就本發明之實施例1 0〜1 2及比較例7、8說明之。 該等實施例及比較例係就數種配合而進行滲透試驗及沉降 試驗,結果如表5所示。Note 2 · After 3 hours, the viscosity did not reach 500 CPS. Thickening time is measured at the liquid temperature of 2 0 C. Hereinafter, Examples 10 to 12 and Comparative Examples 7 and 8 of the present invention will be described. These examples and comparative examples are permeation tests and settling tests for several combinations. The results are shown in Table 5.

第16頁 575532 五、發明說明(12) 【渗透試驗】: 該滲透試驗係將採用豐浦標準砂以相對密度約6 0%充 填於50 X 100 cm之壓克力管内,再加水而使其飽和之 後,將上述代表性之實施例及比較例之配合液以1 k g f / c m 2 之壓力注入,而行測定其滲透距離。豐浦標準砂之充填係 以定量而分開數次進行,每次都以木鎚輕敲壓克力管側 面。再者,配合液之調製係先將A、B兩液裝入攪拌器内施 以攪拌1 0秒者。而滲透距離係以自克力管外面藉由目視所 測定其具有明確顏色變化之範圍,而做為其滲透距離。Page 16 575532 V. Explanation of the invention (12) [Penetration test]: This penetration test will use Fengpu standard sand to fill a 50 X 100 cm acrylic tube with a relative density of about 60%, and then add water to make it After saturation, the compound liquids of the above-mentioned representative examples and comparative examples were injected at a pressure of 1 kgf / cm 2 and the penetration distance was measured. The filling of Toyura Standard Sand is performed several times in a quantitative manner, each time tapping the side of the acrylic tube with a wooden hammer. In addition, the preparation of the mixing liquid is to firstly put the two liquids A and B into the mixer and stir for 10 seconds. The penetration distance is defined as the range of clear color change measured by visual observation from the outside of the acrylic tube.

再者,在注入一週以後,用水將其未固結之部份洗 去,而可依公式求得概算之固結率。尚且,配合液之注入 量係自計晝量扣除注入後之殘餘量之值,又,固結部份之 空隙量係以砂為均勻充填者,而自固結部份之模體之空隙 量扣除砂之充填量以求得。 【公式1】 固結部份之模體之空隙量(ml)—固結部份之砂之充塡量(ml)In addition, one week after the injection, the unconsolidated portion was washed away with water, and the estimated consolidation rate can be obtained according to the formula. In addition, the injection amount of the compounding liquid is the value of the residual amount after the injection is deducted from the day-to-day amount. Also, the void amount of the consolidated part is filled with sand as the uniform, and the void amount of the mold body of the self-consolidated part. Subtract the amount of sand to obtain. [Formula 1] The void amount of the phantom in the consolidation part (ml)-the filling amount of sand in the consolidation part (ml)

固結率(%)=---- xlOO 注入量(ml)Consolidation rate (%) = ---- xlOO injection volume (ml)

【沉降試驗】· 沉降試驗係以攪拌器將配合液攪拌混合1 0秒而行調製 配合液,當以B型黏度計測定其黏度到達5 0 0 c p s之後(在比 較例等之中,不增黏之配合係以配合液調製3 0分鐘之 後),再將其1 0 m 1注入量筒内並予以靜置,且每隔3 0分鐘[Sedimentation test] · The sedimentation test is performed by mixing the mixed liquid with a stirrer for 10 seconds to prepare the mixed liquid. When the viscosity is measured with a B-type viscometer to reach 500 cps (in comparative examples, it does not increase) After mixing for 30 minutes with the mixing solution), inject 10 m 1 into the graduated cylinder and let it stand, and every 30 minutes

第17頁 575532 五、發明說明(13) 離水量無變 藉由目視測定其不含粒子之液量(離水量) 化後,則用該離水量及藉由公式求其沉降率 【公式2】 離水量(ml) 沉降率(%) = ^ —- X 100 最初之配合液量(ml) 【表5】Page 17 575532 V. Explanation of the invention (13) The amount of water does not change. The amount of liquid (particle water) without particles is measured by visual inspection. After the amount of water and the sedimentation rate are calculated by the formula [Formula 2] Amount of water (ml) Settling rate (%) = ^ —- X 100 Initial mixed liquid volume (ml) [Table 5]

實施例 比較例 NO. 配合液 滲透距離 (cm) 固結率 (%) 沉降率 (%) 實一 10 表4之實施例1 100 96 2 實一11 表4之實施例2丨100 99 1 竇一 12 表4之實施例4 65 94 η j 比一 7 表4之比較例2 | 451 1 98 0 比一 8 . 表4之比較例4 15 57 60 第18頁 1 符號表示比較例7係因為增黏迅速而使滲透距離變短者 以下就本發明之實施例1 3〜1 6及比較例9、1 0說明 之。 該等實施例及比較例係就數種配合而於液溫3 0 0 c時測 定其增黏時間,且增黏時間之調整劑(碳酸氫鈉)之使用 量係如表6所示,其他之用量則相同,其結果乃如表6所 示。按此測試結果,即使在高溫之下,其增黏時間亦長’ 而能充分滲透。又於其可塑狀態方面,比較例除外,本發 明之實施例之任一者皆為3 0分鐘以上。 575532 五、發明說明(14) 【表6】 實施例 比較例 NO. 配合液 碳酸氫鈉 (g) 增黏時間 (分) 竇一 13 表4之實施例1 7 80 竇一 14 S 4之實施例2 6 50 實一 15 表4之實施例3 4 115 實一16 表4之比較例6 4 75 比一 9 表4之比較例2 10 20* 比一10 表4之比較例5 20 3* *符號表示以量杯倒立法測定之膠化時間 以下就本發明之實施例1 7、1 8及比較例1 1、1 2說明 之。 該等實施例及比較例係就數種配合而測定其土中膠化 時間及增黏時間(或膠化時間),其結果係如表7所示。 【土中膠化時間測定法】: 本測定法係以攪拌器將配合液攪拌混合1 〇秒而行調製 配合液,隨後即將5 0 g之配合液加入混合於1 〇 〇 g豐浦標準 砂内而後予以靜置,接著將竹串刺入其内再予以拔出之 後,即行測定其竹串刺入過之痕跡之殘留時間,而以此殘 留時間當做土中膠化時間。尚且,亦同時以剩餘之配合液Examples Comparative Example NO. Permeation distance (cm) of compounding solution Consolidation rate (%) Settling rate (%) Example 1 100 Table 2 Example 1 100 96 2 Example 1 Example 2 of Table 4 丨 100 99 1 Sinus 12 12 Example 4 of Table 4 65 94 η j than 1 7 Comparative Example 2 of Table 4 | 451 1 98 0 to 8 8. Comparative Example 4 of Table 4 15 57 60 Page 18 1 The symbol indicates Comparative Example 7 because Those that increase viscosity quickly and shorten the penetration distance are described below with reference to Examples 1 to 16 and Comparative Examples 9 and 10 of the present invention. For these examples and comparative examples, the viscosity increasing time was measured at a liquid temperature of 300 ° C for several combinations, and the amount of the viscosity increasing time adjusting agent (sodium bicarbonate) is shown in Table 6. The amounts are the same, and the results are shown in Table 6. According to this test result, even under high temperature, its thickening time is long and it can fully penetrate. In terms of its plastic state, except for the comparative example, any one of the examples of the present invention is 30 minutes or more. 575532 V. Description of the invention (14) [Table 6] Examples Comparative Example NO. Blending solution sodium bicarbonate (g) Thickening time (minutes) Dou 13 Example of Table 1 7 80 Dou 1 14 S 4 Implementation Example 2 6 50 Example 1 Example 3 of Table 4 4 115 Example 1 Comparative Example 6 of Table 4 4 75 Compared to Example 9 of Table 4 2 10 20 * Comparative Example 5 of Table 4 5 20 3 * The * symbol indicates the gelation time measured by the measuring cup inversion method. Examples 17 and 18 and Comparative Examples 1 and 12 of the present invention will be described below. For these examples and comparative examples, the gelation time and thickening time (or gelation time) in the soil were measured for several combinations. The results are shown in Table 7. [Measurement of gelation time in soil]: This measurement method uses a stirrer to mix and mix the mixed solution for 10 seconds to prepare a mixed solution, and then 50 g of the mixed solution is added to and mixed with 100 g of Fengpu standard sand. Then, let it stand inside, and then pierce the bamboo string into it and then pull it out, and then measure the residual time of the traces of the bamboo string piercing, and use this residual time as the gelation time in the soil. Also, at the same time with the remaining complex solution

第19頁 575532 五、發明說明(15) 測定其增黏時 【表7】 實施例 比較例 NO. 配合液 增黏時間 (分) 土中膠化 時間 (分) 實一17 表4之實施例4 70 >120 實一 18 表4之實施例5 30 110 比一11 表4之比較例2 17* 7 比—12 表4之比較例4 29* 11 *符號表示比 按上述說 及微粒水泥( 由使用特定量 (1 )藉由中性a 微有 入 注盤L、。卩 > <合ΐ 渣之於配獲 炼佳由行可 粒極}而} 較例之膠化時間 明之本發明之地盤固結材,係以中性矽溶膠 及微粒熔渣)做為主成份之地盤固結材,藉 之中性矽溶膠而可獲得以下之功效。 >溶膠之少量添加,而可減低微粒水泥(及 入地盤時之於土粒間之堵塞情形,遂具 滲透性。 f較長之地盤注入時間,遂能以一種液體注 篆液型之高固結強度。Page 19 575532 V. Description of the invention (15) When measuring its thickening [Table 7] Examples Comparative Example NO. Thickening time (minutes) of compounding solution Gelation time (minutes) in soil Example 17 Table 4 4 70 > 120 Example 18 Table 4 5 30 110 Example 11 Table 4 Comparative Example 2 17 * 7 Ratio -12 Comparative Example 4 of Table 4 29 * 11 * The symbol indicates that the ratio is as mentioned above for particulate cement (By using a specific amount (1) by neutral a slightly into the injection disk L, 卩 gt > < combined with the slag for the refining and refining by fine grains} and} the gelation time of the case is clear The site consolidation material of the present invention is a site consolidation material mainly composed of neutral silica sol and particulate slag, and the following effects can be obtained by using neutral silica sol. > The addition of a small amount of sol can reduce the particle cement (and the clogging between soil particles when entering the site, which is permeable. f) Longer the site injection time, it is possible to inject a liquid into the liquid type. Consolidation strength.

第20頁 575532 圖式簡單說明 第22頁Page 575532 Simple Explanation of Drawings Page 22

Claims (1)

575532 六、申請專利範圍 (2 )配合後經過1分鐘以上時,配合液呈可塑狀態,且可 持續維持此可塑狀態達1 〇分鐘以上者。 3 .依申請專利範圍第1或2項所述之地盤固結材料,其係將 瞬結膠結劑預先注入地盤之後,再行當做緩結膠結劑注 入地盤内者。575532 6. Scope of patent application (2) When more than 1 minute has passed after compounding, the compounding liquid is in a plastic state, and the plastic state can be maintained for more than 10 minutes. 3. The site consolidation material according to item 1 or 2 of the scope of the patent application, which is injecting the instant cement into the site in advance, and then injecting it into the site as a retarding cement. 第24頁 申請日期:8’久f丨丨^ IPC分類 申請案號:又7ίΠ〇Γΐ (以上各欄由本局填註) 發明專利說明書 • 575532 中文 地盤固結材料 、 發明名稱 英文 FOUNDATION SOLIDIFYING MATERIALS 姓名 (中文) 1. 三輪求 2. 柏原健二 二 姓名 (英文) 1. Motomu MIWA 2. Kenji KAYAHARA 發明人 (共2人) 國籍 (中英文) 1.日本JP 2.日本JP 住居所 (中文) 1. 日本國東京都文京區本鄉2-15-10 2. 日本國東京都文京區本鄉2-15-10 住居所 (英文) 1. 2. 名稱或 姓名 (中文) 1.日商·強化土工程股份有限公司 名稱或 姓名 (英文) 1.KY0KAD0 ENGINEERING CO., LTD. 三 國籍 (中英文) 1.日本JP 申請人 (共1人) 住居所 (營業所) (中文) 1.曰本國東京都文京區本鄉2-15-10 (本地址與前向貴局申請者相同) 住居所 (營業所) (英文) 1. 1 1 代表人 (中文) 1.島田俊介 代表人 (英文) 1.Shunsuke SHIMADAPage 24 Application Date: 8 '久 f 丨 丨 ^ IPC Classification Application Number: Another 7ίΠ〇Γΐ (the above columns are filled by the Office) Invention Patent Specification • 575532 Chinese Site Consolidation Materials, Invention Name English FOUNDATION SOLIDIFYING MATERIALS Name (Chinese) 1. Three rounds of seeking 2. Name of Kashiwabara 22 (English) 1. Motomu MIWA 2. Kenji KAYAHARA Inventor (total 2 persons) Nationality (Chinese and English) 1. Japan JP 2. Japan JP Residence (Chinese) 1. 2-15-10 Hono, Bunkyo-ku, Tokyo, Japan 2. 2-15-10 Hono, Bunkyo-ku, Tokyo, Japan (English) 1. 2. Name or Name (Chinese) 1. Japanese Business · Name or Name of English for Strengthening Earth Engineering Co., Ltd. (English) 1. KY0KAD0 ENGINEERING CO., LTD. Three Nationalities (Chinese and English) 1. Japanese JP Applicant (1 person in total) Residence (Business Office) (Chinese) 1. 2-15-10 Hongo, Bunkyo-ku, Tokyo, Japan (This address is the same as the applicant who applied to your office before.) Residence (Business Office) (English) 1. 1 1 Representative (Chinese) 1. Shimada Shunsuke Representative (English ) 1. Shunsuke SHIMADA 575532 五、發明說明(16) (4 )因中性矽溶膠並未如一般水玻璃之含有多量高鹼成 份,遂甚少有因鹼成份之溶出而至影響環境之問題。 (5 )縱使使用較多之水泥時,因中性石夕溶膠幾乎不含有如 一般水玻璃之高鹼成份,而使固結物具有良好之耐久 性。 水泥之鈣成份係容易因鹼而溶解於水,但因中性矽溶 膠之使用,遂使鈣成份因與中性矽溶膠間之化學反應而成 為不易溶解於水之化合物(石夕酸#5 ),遂使固結物具有良好 之财久性。575532 V. Description of the invention (16) (4) Because the neutral silica sol does not contain a large amount of high alkali components like ordinary water glass, there are few problems that affect the environment due to the dissolution of alkali components. (5) Even when a large amount of cement is used, the neutral stone sol hardly contains high alkali components such as ordinary water glass, so that the solidified material has good durability. The calcium component of cement is easily soluble in water due to alkali, but the use of neutral silica sol makes the calcium component difficult to dissolve in water due to the chemical reaction with the neutral silica sol (石 夕 酸 # 5 ), So that the consolidation has good financial longevity. 第21頁Page 21
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JP3752672B2 (en) * 2002-06-11 2006-03-08 兼松日産農林株式会社 Construction method of underground improvement body
JP5270819B2 (en) * 2005-06-02 2013-08-21 強化土エンジニヤリング株式会社 Ground strengthening method
KR20190094657A (en) 2018-02-05 2019-08-14 조성광 Composition for ground reinforcing and construction method using the same
KR102226858B1 (en) 2020-04-13 2021-03-10 조성광 Injection material using composition for ground reinforcing

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