TW568946B - Grouting consolidation material - Google Patents

Grouting consolidation material Download PDF

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Publication number
TW568946B
TW568946B TW89124686A TW89124686A TW568946B TW 568946 B TW568946 B TW 568946B TW 89124686 A TW89124686 A TW 89124686A TW 89124686 A TW89124686 A TW 89124686A TW 568946 B TW568946 B TW 568946B
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Taiwan
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silica
solution
water glass
colloidal silica
patent application
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TW89124686A
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Chinese (zh)
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Shunsuke Shimada
Kenji Kashiwabara
Motomu Miwa
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Kyokado Eng Co
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  • Consolidation Of Soil By Introduction Of Solidifying Substances Into Soil (AREA)
  • Soil Conditioners And Soil-Stabilizing Materials (AREA)

Abstract

A grouting consolidation material has high strength and excellent durability in spite of a low silica concentration and exhibits a long gelling time and enables seepage into a wide range as the grout for preventing the liquefaction of ground. A grouting consolidation material is obtained by mixing water glass with colloidal silica at a specified ratio or further mixing the resulting mixture with a specific amount of active silicic acid to form a stabilized alkaline silica solution as the base which is non-self curable in itself or further subjecting the resulting alkaline silica solution to dealkalization treatment to form a dealkalized silica solution as the base, and further adding an acidic reactant, another reactant, cement, slag and the like to the base.

Description

568946 A7 _ B7 五、發明說明(1 ) 【發明所屬技術領域】 本發明係提供一種地面注入用固結材,乃相關將含有 高莫耳比之膠體氧化矽及水玻璃(甚至含活性矽酸)的氧 化矽溶液作爲底盤,並以低氧化矽濃度維持廣範圍凝膠化 時間的地面注入固結材,特別係在.施行防止地面液化的注 入處理時,可經由長時間連續注入而改善大面積地面,同 時具高凝固強度,且固結性優越,更具良好的水土保持性 之地面注入固結材。 【習知技術】 按,一般由水玻璃與膠體氧化矽所混合而成的地面注 入材料,如眾所週知的具有良好的固結體耐久性之優點, 但是將3號水玻璃大量混合入膠體氧化矽的話,將瞬間轉 成凝膠化。 習知爲避免此種瞬間凝膠化現象產生,譬如便有將高 莫耳比的水玻璃與膠體氧化矽混合,而形成具自硬性的地 面注入液,此乃眾所皆知的技術。 【發明欲解決課題】 惟,此類型注入液因爲氧化矽濃度過高,反而無法呈 現高固結強度。同時,若將其作爲1 · 5注射量( s h 〇 t )或2 · 0注射量的單邊液(A液)使用時,因 爲屬自身凝膠化者,造成使用上受到限制。 有鑑於斯,本發明遂開發一種將水玻璃與膠體氧化砂 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) (請先閱讀背面之注意事項再Hi 本頁) --線· 經濟部智慧財產局員工消費合作社印製 -4 - 568946 A7 __ B7 五、發明說明(2 ) 、或者將水玻璃、膠體氧化矽與活性矽酸的調配成分加以 限定,在調配該等成分時,於注入地面之前,選定不致造 成本身凝膠化的特定調配比例或S i 0 2濃度,同時在土地 中保持廣範圍的凝膠化時間,特別係保持長時間的凝膠化 時間,且可減少因長時間連續注入土粒間時容易產生的土 粒間凝膠體氧化矽沉澱,而所造成的滲透性降低現象發生 之具優越性的防止地面液化用地面注入固結材。此種本發 明固結材,係以較地的S i〇2濃度便可顯示較高的固結強 度,同時未反應水玻璃或反應性生成物亦將較少,在水土 保持上亦具良好功效者。 緣是,本發明之目的在於提供一種將高莫耳比之膠體 氧化矽及水玻璃(甚至含活性矽酸)的氧化矽溶液作爲底 盤,並以低氧化矽濃度維持廣範圍凝膠化時間,同時在施 行防止地面液化的注入處理時,可經由長時間連續注入而 改善大面積地面,同時具高凝固強度,且固結性優越,更 具良好的水土保持性之已改善上述習知諸項缺失的地面注 入固結材。 【課題解決之手段】 職是,爲達上述本發明之目的,故所提供的技術特徵 在於由含有膠體氧化矽與水玻璃,且在注入地面之前,本 身不產生凝膠化的鹼性氧化矽溶液所組成,其中該溶液中 的S i〇2濃度爲3〜1 3重量%,而源自膠體氧化矽中的 31〇2量則爲1〜50重量%。 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) _ 5 - ί I I I —Γ I I —Γ I I I · I I (請先閱讀背面之注意事項再β本頁) ·- --線· 經濟部智慧財產局員工消費合作社印製 568946 A7 B7 經濟部智慧財產局員工消費合作社印製 五、發明說明(3 ) 此外,爲達上述本發明之目的,故亦提供另一技術, 其技術特徵在於屬含有膠體氧化矽、水玻璃與活性矽酸的 鹼性氧化矽溶液,其中該溶液中的S i 0 2濃度爲3〜1 3 重量%,而源自膠體氧化矽中的S i 〇2量則爲1〜5 0重 量%。 【發明實施較佳態樣】 以下,針對本發明進行詳細說明。 相關本發明的地面注入用固結材係如上述,乃爲調配 成分爲膠體氧化矽與水玻璃(甚或除此二種化合物外,更 包含有氧化矽)的鹼性氧化矽溶液。 上述膠體氧化矽乃爲呈膠質狀性質,若單獨時則屬具 備有半永久性之不凝膠化的穩定物質。其製造例之一例敘 述如後。 首先,將水玻璃之水稀釋液,利用離子交換樹脂或離 子交換層,進行脫鹼處理,而獲得P Η 2〜4的活性矽酸 0 ' 其次,在所製得活性矽酸中,添加水玻璃、苛性鹼等 鹼劑,並將ρ Η値調整爲8 · 5〜1 0左右的鹼性液,且 將S 1〇2濃度調整爲3〜5%左右後,在70〜9 5°C溫 度下,施行加熱1〜5小時左右的加熱、製粒處理後,便 可製得膠體氧化矽母液。通常均將該母液濃縮至S i 0 2濃 度爲2 0〜3 0%,而成爲最終膠體氧化矽,但在本發明 中,可直接使用該母液作爲膠體氧化矽。 (請先閲讀背面 之注—再壽 本頁) •線. 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) -6 - 568946 A7 _____ B7 經濟部智慧財產局員工消費合作社印製 五、發明說明(4 ) 本發明中所採用的水玻璃係鹼金屬矽酸鹽水溶液,以 s i〇2/Na2〇所表示的莫耳比,最好爲3 · 4以上的 較高莫耳比爲佳,當然只要在經膠體氧化矽與活性矽酸混 合後不致產生凝膠化的範圍下,可採用任意的莫耳比率。 本發明中所使用的活性矽酸,係將水玻璃經離子交換 樹脂處理、或經離子交換層處理,而去除水玻璃中的鹼成 分’並利用將p Η値調整低於水玻璃方式而製得。 通常,在上述水玻璃與膠體氧化矽的混合系中、或該 等與活性矽酸的混合系中,氧化矽(S i 0 2濃度)若較濃 的話,則將容易造成電性不穩定狀態,所以,氧化矽將電 性不均質的聚集,造成有局部較弱的情形產生,變成很難 形成具均質強度的凝膠。 在上述混合系中,在注入於地面前的調配時,即便將 凝膠化時間調整變長,於注入後,在地面中不均質析出氧 化矽,便將沉澱於土粒間而形成顆粒,造成滲透性降低的 現象,因此將造成注入壓過大,或形成龜裂而外逸,致無 法獲得廣範圍均質的如設計之初所期待的固結效果。 特別係在施行防止地面液化處理時,必須具經濟效益 的改良大面積土地,所以便將注入孔間隔拓廣,同時平均 一注入點必須進行數小時或數十小時的連續注入處理。 本發明爲更正上述不合理情形,便提供一種在水玻璃 與膠體氧化矽的混合系中,或該等與活性矽酸的混合系中 ,於將混合液注入地面前,本身不產生凝膠化的穩定物質 ,並決定出維持此種穩定狀態的條件。 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) (請先閱讀背面之注意事項再 · 11 本頁) 訂· -•線- 568946 A7 ___ Β7 五、發明說明(5 ) 即,本發明係在上述含有膠體氧化矽與水玻璃之鹼性 氧化矽溶液中,將該溶液中的S i 0 2濃度設定爲稀釋至3 〜1 3重量%,且其中源自膠體氧化矽的S i〇2量設定爲 1〜5 〇重量%,最好設定爲3〜5 0重量%,藉此在注 入地面前,本身幾乎呈現半永久性|不凝膠化的穩定固結材 料。另,相對於水玻璃量,即便膠體氧化矽量較多量時, 亦存在有屬穩定化的範圍。該範圍因爲隨水玻璃與膠體氧 化矽的種類而各有不同,所以很難一言載明,不過大致上 可認爲全部S i〇2量中,源自膠體氧化矽的S i〇2量約 略在9 0%以上左右者。 此外,本發明亦在上述含有膠體氧化矽、水玻璃與活 性矽酸之鹼性氧化矽溶液中,將該溶液中的S i〇2濃度設 定爲稀釋至3〜1 3重量%,且其中源自膠體氧化矽的 S i〇2量設定爲1〜5 0重量%,最好設定爲3〜5 0重 量% ’藉此在注入地面前,本身幾乎呈現半永久性不凝膠 化的穩定固結材料。 上述中,膠體氧化矽與活性矽酸的比率,隨隨該等種 類的不同而互異,但最好將源自活性矽酸的S i 0 2量保持 在約略5 0重量%以下的比率。 上述鹼性氧化矽溶液係將膠體氧化矽或活性矽酸中的 其中一部分,藉由水玻璃的鹼性而溶解,結果構成該溶液 的氧化矽粒徑,便形成由膠體氧化矽的保持粒徑起,到在 水玻璃之氧化矽中可見的矽酸分子粒徑爲止的粒徑分布之 商莫耳比氧化矽溶液。該莫耳比較.水玻璃的莫耳比爲高 本紙張尺度適用中國國家標準(CNS)A4規格(210x297公爱)· (請先閱讀背面之注意事項再 本頁) 經濟部智慧財產局員工消費合作社印製 568946 A7 B7 五、發明說明(6 ) 但較膠體氧化矽或活性矽酸的莫耳比爲低。 若上述鹼性氧化矽溶液的S i〇2濃度在3〜1 3重量 %範圍之外,換句話說,即當小於3重量%時,S 1 〇2量 過少而將導致固結強度變小,反之,若大於1 3重量%時 ,將因S i 〇2量過多,造成本身凝膠化,而無法維持穩定 性。 . 再者,若源自膠體氧化矽的S i〇2量,或源自膠體氧 化矽與活性矽酸的s i〇2量,在1〜5 0重量%範圍外的 話,即若小於1重量%的話,雖凝膠化時的固結物在初期 的強度將變大,但大多數其長期強度卻將較低,且耐久性 亦將惡化,同時土中凝膠化時間亦將逐漸縮短;反之,若 大於5 0重量%時,則固結物的初期強度將變小。 在相對水玻璃量中,企圖藉由增加膠體氧化矽量,而 達穩定化功效時,固結物在初期強度將非常低,雖不是良 好的普通水泥漿,但若將土中凝膠化時間維持較長的話, 卻足夠作爲防止地面液化用固結材使用。 本發明之鹼性氧化矽溶液係鈉的含量較少,所以採用 如離子交換樹脂或離子交換層的柱體等小規模裝置,在現 場比較容易進行脫鹼處理,同時亦可形成活性較大的脫鹼 氧化矽溶液。該脫鹼氧化矽溶液,可獲得本身並不凝膠化 系統之物質,或獲得經長時間後才會產生凝膠化系統之物 質。經長時間後才會產生凝膠化系統之物質,其若單獨使 用,便屬良好的防止液化用注入材。 在本發明中,可於上述鹼性氧化矽溶液、或脫鹼氧化 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) -9 - (請先閱讀背面之注意事項再θ本頁) 訂· 丨線. 經濟部智慧財產局員工消費合作社印製 568946 A7 B7 五、發明說明(7 ) 矽溶液中,添加反應劑混合。該反應劑可舉例如硫 酸、氯化鋁、聚氯化鋁、硫酸類、有機酸(檸檬酸 酸、醋酸等)等等在水溶液中呈酸性的各種酸性反 或如鹼金屬鹽類、鹼土金屬鹽類等無基鹽類、水泥 、石灰類、石膏等。 譬如在鹼性氧化矽溶液中添加酸性反應劑,而 液調整爲酸性〜中性區域,便可成爲具特定特定凝 間的水泥漿。此情況時,即便不再添加如硫酸類之 而採用如磷酸、氯化鋁、聚氯化鋁、硫酸類、有機 性反應劑時,在土中的凝膠化時間縮短情形亦非常 且強度亦非常佳,所以可供作可橫跨廣範圍之地面 固結材用,尤其是一種良好的液化防止用固結材。 再者,藉由在鹼性氧化矽溶液或脫鹼氧化矽溶 添加比較少量的各種反應劑,便可獲得橫跨廣範圍 化時間(特別是凝膠化時間較長),且土中凝化時 縮短的固結材料。此情況下所製得的固結材料,不 越的滲透性,且固結物持久性亦佳,同時以稀薄的 濃度便可展現較高的強度,更可提早顯現出強度。 酸、磷 、琥珀 應劑, 、爐渣 將該溶 膠化時 強酸, 酸等酸 有限, 注入用 液中, 的凝膠 間不致 僅具優 氧化矽 (請先閱讀背面之注意事項再 —襄· 獅本 頁) . 線. 經濟部智慧財產局員工消費合作社印製 【發明的實施例】 以下’雖針對本發明實施例進行詳述,惟本發明並不 僅限於該等實施例。 •使用 568946 A7 B7 五、發明說明(8 ) (1 )活性矽酸 將水玻璃J I s 3號產品(旭電化公司(股)出品, S i 〇 2 ·· 2 9 · 0 %、N a 2 〇·· 9 · 0 % ),以水進行 稀釋,而獲得S i〇2: 5 , 8%、Na2〇:1 · 8%的 稀釋物。將其通過氫型陽離子交換樹脂(才义方乂公司( 股)出品,7 A —歹4卜I R — 1 2 Ο B )塔中經脫鹼 處理後,便可獲得S i〇2 : 5 · 8 %、P Η値3 · 〇的活 性矽酸。(該活性矽酸隨脫鹼程度,可獲得廣範圍ρ Η値 者) (2 )膠體氧化矽 將上述活性矽酸丟入鹼水中,而形成S i 0 2濃度4 % 、Ρ Η値9 · 0後,加熱至9 0 °C,並攪拌2小時後,便 可獲得膠體氧化矽母液。使用將該母液經濃縮而所獲得的 S i〇2含量爲20%與30 · 1%的膠體氧化矽。該膠體 氧化矽的平均粒徑爲4微米與5微米。其性質如表1中所 不° 【表1 : No. 比重 Sl〇2 (%) pH 平均粒徑 (微米) 1 1.20 30.1 9.8 15 2 1.13 20.0 10.1 4 (3 )水玻璃 普通的水玻璃係採用如下(a )所示:ί Ϊ S 3號水玻 (請先閱讀背面之注意事項再 I · I I 本頁) Ηδτ. --線. 經濟部智慧財產局員工消費合作社印製 本紙張尺度適用中國國家標準(CNS)A4規格(210 x 297公釐) -11 - (4 )氯化鉀 氯化鈣 磷酸 碳酸氫鈉 568946 A7 _B7 _ 五、發明說明(9 ) 璃,而較高莫耳比的水玻璃則採用如下(b )所示 J I S 5號水玻璃。 (a ) 3號水玻璃:比重(2 0 °C ) 1 · 3 9、 S ι〇2量29 · 2%、Na2〇量9 · 5%、莫耳比 3 .17%之JI S3號水玻璃 (b ) 5號水玻璃:比重(2 0 °C ) 1 · 3 2、 S i〇2量29 · 2%、Na2〇量7 · 03%、莫耳比 3 · 75%之J I S5號水玻璃 一級試藥 一級試藥 一級試藥 一級試藥 聚氯化鋁 J I S規格 (5 )水泥 採用如表2中所示的組成與粉碎度不同的波特蘭水泥 與高爐水泥。 (請先閱讀背面之注意事項再 --- 魏本頁) --線· 經濟部智慧財產局員工消費合作社印製 【表2】 水泥種類 Si〇2 (%) Ah〇3 (%) F e 2 0 3 (%) Ca〇 (%) Mg〇 (%) 驗基 度 水硬 率 布氏比面 値(cm2/g) 1 波特蘭 水泥 21.9 5.3 3.1 65.1 1.4 3.28 2.15 3,200 2 局爐水 泥 25.8 9.4 2.0 54.9 3.4 2.61 1.47 9,700 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 12- 568946568946 A7 _ B7 V. Description of the Invention (1) [Technical Field of the Invention] The present invention provides a consolidation material for ground injection, which is related to colloidal silica and water glass (even containing active silicic acid) containing high molar ratios. ) Silicon oxide solution as the chassis, and low-silicon oxide concentration to maintain a wide range of gelation time of the ground into the consolidation material, especially when the implementation of the ground to prevent the liquefaction of the injection treatment, can be improved by continuous injection for a long time. The area of the ground, at the same time has a high solidification strength, and excellent consolidation properties, more good soil and water retention of the ground into the consolidation material. [Known technology] According to the general, ground injection materials made of water glass and colloidal silica are well-known. They have the advantages of good solidity durability, but a large amount of water glass is mixed into colloidal silica. If it does, it will instantly turn into gel. It is known to avoid this kind of instant gelation phenomenon. For example, it is known to mix high-mole ratio water glass with colloidal silica to form a self-hardening ground injection solution. [Invention aims to solve the problem] However, this type of injection solution cannot exhibit high consolidation strength because the concentration of silicon oxide is too high. At the same time, if it is used as a single injection (Liquid A) of 1.5 injection volume or 2.0 injection volume, it is restricted in use because it is a gelling agent. In view of this, the present invention has developed a paper that uses water glass and colloidal oxidized sand. The paper size is applicable to the Chinese National Standard (CNS) A4 (210 X 297 mm) (please read the precautions on the back first, then Hi this page)- Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs-4-568946 A7 __ B7 V. Description of the Invention (2), or limiting the composition of water glass, colloidal silica and active silicic acid At the same time, before injecting into the ground, select a specific blending ratio or S i 0 2 concentration that does not cause gelation itself, while maintaining a wide range of gelation time in the ground, especially to maintain a long gelation time, and It can reduce the permeability caused by the reduction of the permeability of the silica particles which is easily generated when the soil particles are continuously injected into the soil particles for a long time. Such a consolidation material according to the present invention can show a higher consolidation strength at a lower Sio2 concentration, and at the same time, there will be less unreacted water glass or reactive products, and it will also have good soil and water conservation. Efficacy. The reason is that the purpose of the present invention is to provide a colloidal silica with high molar ratio and a silica solution of water glass (even containing active silicic acid) as a chassis, and maintain a wide range of gelation time with a low silica concentration. At the same time, when the injection treatment to prevent ground liquefaction is performed, a large area of the ground can be improved through continuous injection for a long time. At the same time, it has high solidification strength, excellent consolidation, and better soil and water retention. The missing floor is filled with consolidation material. [Means for solving problems] In order to achieve the above-mentioned object of the present invention, the technical feature provided is that it contains colloidal silica and water glass, and does not generate gelated alkaline silica itself before it is injected into the ground. It is composed of a solution, in which the Sio2 concentration in the solution is 3 to 13% by weight, and the amount of 3102 in the colloidal silica is 1 to 50% by weight. This paper size is in accordance with China National Standard (CNS) A4 (210 X 297 mm) _ 5-ί III —Γ II —Γ III · II (Please read the precautions on the back before β page) ·---- Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs 568946 A7 B7 Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs V. Invention Description (3) In addition, in order to achieve the above-mentioned object of the present invention, another technology is also provided. It is characterized in that it is an alkaline silica solution containing colloidal silica, water glass and active silicic acid, wherein the concentration of S i 0 2 in the solution is 3 to 13% by weight, and S i derived from colloidal silica. The amount of 2 is 1 to 50% by weight. [A preferred embodiment of the invention] Hereinafter, the present invention will be described in detail. The above-mentioned consolidation material for floor injection according to the present invention is an alkaline silica solution prepared by colloidal silica and water glass (or even containing these two compounds, in addition to these two compounds) as described above. The above colloidal silica is colloidal in nature, and when it is alone, it is a semi-permanent non-gelatinous stable substance. An example of the manufacturing example is described later. First, dilute the water glass with water and use an ion-exchange resin or an ion-exchange layer to perform alkali removal treatment to obtain P Η 2 ~ 4 active silicic acid 0 ′. Second, add water to the prepared active silicic acid Alkali agents such as glass, caustic alkali, etc., adjust ρ 的 to an alkaline solution of about 8. 5 to 10, and adjust the concentration of S 10 2 to about 3 to 5%, then at 70 to 9 5 ° C After heating and granulating for about 1 to 5 hours at a temperature, a colloidal silica mother liquor can be obtained. Usually, the mother liquor is concentrated to a Si 0 2 concentration of 20 to 30% to become the final colloidal silica. However, in the present invention, the mother liquor can be directly used as the colloidal silica. (Please read the note on the back-re-live this page first) • Thread. This paper size is applicable to Chinese National Standard (CNS) A4 (210 X 297 mm) -6-568946 A7 _____ B7 Employee Consumer Cooperative of Intellectual Property Bureau, Ministry of Economic Affairs Printing 5. Description of the invention (4) The molar ratio of the water glass alkali metal silicate aqueous solution used in the present invention, expressed as si〇2 / Na2〇, is preferably a higher than 3 · 4. The ear ratio is better. Of course, any mole ratio can be used as long as it does not cause gelation after mixing colloidal silica and active silicic acid. The active silicic acid used in the present invention is prepared by treating water glass with an ion exchange resin or an ion exchange layer to remove alkali components in the water glass and adjusting the p p to be lower than that of the water glass. Got. In general, in a mixed system of the above-mentioned water glass and colloidal silica, or in a mixed system with active silicic acid, if the silicon oxide (S i 0 2 concentration) is relatively thick, it will easily cause an electrical instability state. Therefore, silicon oxide aggregates electrically inhomogeneously, resulting in a locally weak situation, and it becomes difficult to form a gel with homogeneous strength. In the above-mentioned mixed system, even when the gelation time is adjusted to be longer during the preparation before injecting into the ground, after the injection, the silicon oxide is heterogeneously precipitated in the ground, and it will settle between the soil particles to form particles, resulting The phenomenon of reduced permeability will cause excessive injection pressure, or cause cracks to escape, resulting in a wide range of homogeneous consolidation effects as expected at the beginning of the design. Especially in the implementation of the prevention of ground liquefaction, a large area of land must be improved economically, so that the interval between injection holes is widened, and meanwhile, an injection point must be continuously injected for several hours or tens of hours. In order to correct the above-mentioned unreasonable situation, the present invention provides a mixed system of water glass and colloidal silica, or these mixed systems with active silicic acid, which does not gel itself before the mixed solution is injected into the ground. And determine the conditions for maintaining this stable state. This paper size applies to China National Standard (CNS) A4 (210 X 297 mm) (Please read the precautions on the back before this page · 11 pages) Order ·-• Line-568946 A7 ___ Β7 V. Description of the invention (5) That is, the present invention is based on the above-mentioned alkaline silica solution containing colloidal silica and water glass, and the S i 0 2 concentration in the solution is set to be diluted to 3 to 13% by weight, and the colloidal silica is derived from the colloidal silica. The amount of Si02 is set to 1 to 50% by weight, and preferably to 3 to 50% by weight, so that it is almost semi-permanent | non-gelated stable consolidation material before being injected into the ground. In addition, even when the amount of colloidal silica is relatively large with respect to the amount of water glass, there is a range in which it is stabilized. This range varies depending on the type of water glass and colloidal silica, so it is difficult to specify this range. However, it can be considered that the total amount of S i〇2 derived from colloidal silica out of the total amount of S i02 About 90% or more. In addition, the present invention also sets the Sio2 concentration in the alkaline silica solution containing colloidal silica, water glass, and activated silicic acid to be diluted to 3 to 13% by weight, and wherein the source is The Sio2 content of the self-colloidal silicon oxide is set to 1 to 50% by weight, and preferably to 3 to 50% by weight. 'As a result, it is almost semi-permanent non-gelatinized and stable consolidation before being injected into the ground. material. In the above, the ratio of colloidal silica to active silicic acid varies depending on these types, but it is preferable to keep the amount of Si02 derived from active silicic acid at a ratio of approximately 50% by weight or less. The alkaline silica solution mentioned above dissolves a part of colloidal silica or active silicic acid by the alkalinity of water glass. As a result, the particle size of the silicon oxide constituting the solution is formed by the retained particle size of the colloidal silica. The quotient of the particle size distribution up to the particle size of the silicic acid molecule that can be seen in the silicon oxide of water glass is a molar ratio silica solution. The Mohr comparison. The Mohr ratio of water glass is high. The paper size is applicable to the Chinese National Standard (CNS) A4 specification (210x297). (Please read the precautions on the back before this page.) Consumption by employees of the Intellectual Property Bureau of the Ministry of Economic Affairs Printed by the cooperative 568946 A7 B7 5. Description of the invention (6) However, the molar ratio is lower than colloidal silica or active silicic acid. If the Si02 concentration of the above-mentioned alkaline silica solution is outside the range of 3 to 13% by weight, in other words, when it is less than 3% by weight, the amount of S1 02 is too small and the consolidation strength will be reduced. On the contrary, if it is more than 13% by weight, the amount of S i 〇2 will be excessive, which will cause gelation itself, and stability cannot be maintained. Furthermore, if the amount of Si02 derived from colloidal silica, or the amount of SiO2 derived from colloidal silica and active silicic acid, is outside the range of 1 to 50% by weight, that is, if it is less than 1% by weight If the strength of the solidified substance during gelation will increase at the initial stage, the long-term strength will be lower and the durability will be worsened. At the same time, the gelation time in the soil will gradually decrease; otherwise If it is more than 50% by weight, the initial strength of the consolidated material will be reduced. In the relative amount of water glass, when it is attempted to stabilize by increasing the amount of colloidal silica, the initial strength of the consolidated material will be very low. Although it is not a good ordinary cement slurry, if the soil is gelled in time, If it is maintained for a long time, it is sufficient as a consolidation material for preventing liquefaction on the ground. The alkaline silica solution of the present invention has less sodium content, so using a small-scale device such as an ion-exchange resin or a column of an ion-exchange layer, it is relatively easy to perform alkali treatment on the site, and at the same time, it can form a more active Dealkali silica solution. The dealkaliated silica solution can obtain a substance that does not itself gel a system, or a substance that does not produce a gel system after a long time. The gelation system will not be produced after a long time, and if used alone, it is a good injection material for preventing liquefaction. In the present invention, the Chinese standard (CNS) A4 specification (210 X 297 mm) can be applied to the above-mentioned alkaline silica solution or de-alkali oxidation of this paper. -9-(Please read the precautions on the back before θ This page) Order · 丨. Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs, printed 568946 A7 B7 V. Description of the invention (7) Add a reagent to the silicon solution. The reactants can be, for example, sulfuric acid, aluminum chloride, polyaluminum chloride, sulfuric acid, organic acids (citric acid, acetic acid, etc.) and various acidic reactions which are acidic in aqueous solution, such as alkali metal salts, alkaline earth metals, etc. Non-base salts such as salt, cement, lime, gypsum, etc. For example, if an acidic reactant is added to an alkaline silica solution, and the solution is adjusted to an acidic to neutral region, it can become a cement slurry with a specific specific volume. In this case, even if sulfuric acid is no longer added, and if phosphoric acid, aluminum chloride, polyaluminum chloride, sulfuric acid, or organic reactant is used, the gelation time in the soil is shortened and the strength is also very strong. Very good, so it can be used as a ground consolidation material that can span a wide range, especially a good liquefaction prevention consolidation material. In addition, by adding a relatively small amount of various reagents to an alkaline silica solution or a debasic silica solution, a wide range of time (especially a longer gelation time) can be obtained, and the soil coagulates. Shortened consolidation material. In this case, the consolidated material has not only improved permeability, but also the durability of the consolidated material. At the same time, it can show higher strength with thinner concentration, and it can show strength earlier. Acids, phosphorus, amber, slag, slag, strong acid when the sol, acid and other acids are limited, the injection of the liquid, the gel does not have only excellent silica (please read the precautions on the back before-Xiang · Lion (This page). Line. Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs [Inventive Examples] The following 'is described in detail for the embodiments of the present invention, but the present invention is not limited to these embodiments. • Using 568946 A7 B7 V. Description of the invention (8) (1) Activated silicic acid will be the water glass JI s No. 3 product (produced by Asahi Denka Co., Ltd., S i 〇 2 ·· 2 9 · 0%, N a 2 9.0 · 0%), diluted with water, to obtain a dilution of Si02: 5, 8%, Na20: 1.8%. After passing it through a hydrogen-type cation exchange resin (produced by Caiyi Fangye Co., Ltd., 7 A — A4 歹 IR — 1 2 〇 B) in the tower, it can obtain S i〇2: 5 · 8%, P Η 値 3 · 〇 active silicic acid. (The active silicic acid can be obtained with a wide range of pH depending on the degree of debasicization.) (2) Colloidal silica throws the above active silicic acid into alkaline water to form S i 0 2 with a concentration of 4% and P Η 値 9 · After 0, heating to 90 ° C, and stirring for 2 hours, a colloidal silica mother liquor can be obtained. Colloidal silica having a Sio2 content of 20% and 30.1% obtained by concentrating the mother liquor was used. The colloidal silica has an average particle diameter of 4 microns and 5 microns. Its properties are as shown in Table 1. [Table 1: No. Specific gravity S102 (%) pH average particle size (micron) 1 1.20 30.1 9.8 15 2 1.13 20.0 10.1 4 (3) Water glass ordinary water glass is used As shown in (a) below: Ϊ Ϊ S No. 3 water glass (please read the precautions on the back before I and II on this page) Ηδτ. --Line. This paper is printed by the Consumer Cooperatives of Intellectual Property Bureau of the Ministry of Economic Affairs. National Standard (CNS) A4 Specification (210 x 297 mm) -11-(4) Potassium Chloride Calcium Chloride Phosphate Sodium Bicarbonate 568946 A7 _B7 _ V. Description of the Invention (9) Glass with higher molar ratio For water glass, JIS No. 5 water glass shown in (b) below is used. (a) No. 3 water glass: specific gravity (20 ° C) 1 · 39, SiO 2 content 29 · 2%, Na 2 0 content 9 · 5%, mol ratio 3.17% of JI S3 water Glass (b) No. 5 water glass: specific gravity (20 ° C) 1 · 3 2, S i〇2 content 29 · 2%, Na2 0 content 7. 03%, Mohr ratio 3 · 75% JI S5 The water glass first-level reagent, first-level reagent, first-level reagent, first-level reagent, polyaluminum chloride (JIS) specification (5), cement, as shown in Table 2, uses Portland cement and blast furnace cement with different compositions and pulverization degrees. (Please read the precautions on the back before --- Wei page)-Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs [Table 2] Cement type Si〇2 (%) Ah〇3 (%) F e 2 0 3 (%) Ca〇 (%) Mg〇 (%) Brinell specific surface hydraulic modulus (cm2 / g) 1 Portland cement 21.9 5.3 3.1 65.1 1.4 3.28 2.15 3,200 2 Blast furnace cement 25.8 9.4 2.0 54.9 3.4 2.61 1.47 9,700 This paper size applies to China National Standard (CNS) A4 (210 X 297 mm) 12- 568946

五、發明說明(1〇) 表2中水泥種類N 〇 · 2之高爐水泥的平均粒徑約爲 3微米。 (請先閱讀背面之注意事項再1^本頁) (6 )爐渣 採用如表3中所示組成的爐渣。V. Description of the invention (10) The average particle size of the blast furnace cement of the cement type No. 2 in Table 2 is about 3 microns. (Please read the precautions on the back first, then 1 ^ this page) (6) Slag Use slag with the composition shown in Table 3.

Si〇2 (%) 〆、^ Λ Ah〇3 (%) Fe2〇3 (%) Ca〇 (%) Mg〇 (%) 鹼基度 水硬率 布氏比面値 (cm2/g) 31.4 18.6 1.0 46.2 1.3 2.11 0.91 15,000 (7 )砂 細砂係採用豐浦標準砂,粉土質砂係採用日本千葉縣 產的海砂。 2 ·測量 (1 )砂凝膠單軸壓縮強度 將豐浦標準砂的砂凝膠,利用聚偏二氯乙烯予以密閉 密封(2 0 °C )後,在依照土質工學會基準「泥土之單軸 經濟部智慧財產局員工消費合作社印製 壓縮測試方法」進行測量。 (2 )凝膠化時間 (a )均質凝膠之凝膠時間 依照2 0 °C中的倒杯法進行測量。 (b ) 土中凝膠化時間 在2 〇 °C中,混合水泥漿液與砂後,靜置,捨棄上層 澄淸部分,以竹串刺入砂中再拔出,以痕跡殘留期間爲土 -13- 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 568946 A7 B7 五、發明說明(11 ) 中凝膠化時間,測量該時間。 (3 ) p Η 値 利用玻璃電極ρ Η計進行測量。 3.鹼性氧化矽溶液 將膠體氧化矽與水玻璃予以混合、或將膠體氧化砂、 活性矽酸與水玻璃予以混合後,而製得鹼性氧化矽溶液。 該等化合物的混合比率、與混合液中的S i〇2濃度、源自 膠體氧化矽的S i 0 2量(% )或源自膠體氧化矽與活性矽 酸的S i〇2量(% )、以及穩定性,如表4中所示。 (請先閱讀背面之注意事項再 裝___ 本頁) 訂·· •線· 經濟部智慧財產局員工消費合作社印製 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) -14 - 568946 A7 B7 五、發明說明(^) 經濟部智慧財產局員工消費合作社印製 I 鹼性氧化矽溶液 穩定性 未凝膠化 未凝膠化 未凝膠化 未凝膠化 未凝膠化 未凝膠化 未凝膠化 未凝膠化 未凝膠化 未凝膠化 4〜5個月後呈半凝膠化狀態 Si〇2(%) 与經 靡赳 皿齔 1 1 1 1 1 1 1 1 1 21.4 1 源自膠體 氧化矽 oo 〇〇 〇〇 VO 〇〇 〇 43.9 20.5 28.2 40.7 92.6 1 54.1 Total CN1 1/S vyS 〇〇 r- 〇 m cn5 r Ή 寸 ο 13.9 混合比率(每1000g) 水(g) ο ON 〇 〇〇 〇 〇〇 〇 〇〇 〇 〇 Ο wo ο ι〇 νο 〇 〇 i活性矽酸 1 (g) 1 1 1 儀 1 1 1 1 1 〇 1 1 水玻璃(g) m 〇\ σ\ 〇〇 On r—Η 1 f i 1 〇 1 〇 cn C^l cn 1 1 1 〇 1 〇 CSI 1 ο CO 1 1 1 ,膠體氧化矽(g) 表1中No · CN1 ν_·Η CN 1 τ—Η 1 1 1 1 1 τ—Η 1 1 Ο 1 1 〇 ,丨 i 1 cn OQ 鹼性氧化 矽溶液 比較例1 比較例2 實施例1 實施例2 實施例3 實施例4 實施例5 實施例6 實施例7 實施例8 比較例3 (請先閱讀背面之注意事項再 像 — I 本頁) •線· 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 568946 A7 B7 五、發明說明(13) 由表4中,鹼性氧化矽溶液中的S i〇2濃度以約1 3 %爲界限,在此程度以下並未產生凝膠化現象,呈半永久 用的穩定狀態。故,該等鹼性氧化矽溶液可長期保存,而 可進行與水泥漿原料相同的處置,由工場搬運至待注入現 場。在1 3 %以上的比較例3中,於4〜5個月後便呈半 凝膠化狀態。 此外,在比較例3中,源自膠體氧化矽的S i〇2量亦 超過本發明所限定的範圍,當利用反應劑進行凝膠化時, 便產生強度顯現較遲緩的缺點。 所以,S i〇2濃度只要在略低於1 3 %以下的話,幾 乎均可獲得穩定的鹼性氧化矽溶液。 在比較例1、2中,源自膠體氧化矽的S i〇2濃度在 1 %以下,另在比較例1中,全部S i〇2量亦在3 %以下 ,均屬超過本發明所限定的範圍値。此等當然不致產生凝 膠化屬穩定者。但是,如後述,隨反應劑的添加所獲得之 固結物便將非常的柔軟,S 1 0 2濃度爲3 %左右的界限’ 若在此程度以下的話,強度便將明顯的下降。 實施例7係與截至實施例6爲止的方式相反’屬以大 量膠體氧化矽而呈穩定化的例子。實施例8中則混入少量 活性矽酸,而呈穩定化的例子。此時,源自膠體氧化矽與 活性矽酸中之S 1〇2量中活性矽酸的S i〇2濃度’爲 27·8%,屬在50%以下者。 4 ·脫鹼氧化矽溶液 (請先閱讀背面之注意事項再 本頁) 經濟部智慧財產局員工消費合作社印製 本紙張尺度適用中國國家標準(CNS)A4規格(210x297公釐) -16 - 568946 A7 B7 經濟部智慧財產局員工消費合作社印制衣 五、發明說明(14) 將上述鹼性氧化矽溶液,利用離子交換樹脂或離子交 換層進行脫鹼處理,而製得脫鹼氧化矽溶液。 將表4之實施例4中所得鹼性氧化矽溶液5,0 0 0 ml ,以陽離子交換樹脂9 0 0 m 1進行混合處理後,便 可獲得p Η値3 · 5的脫鹼氧化砍溶液。該脫鹼氧化砂溶 液係S i〇2濃度7 · 1 %,且以約3 0〜3 5小時產生凝 膠化。 此外,取代陽離子交換樹脂處理,改用陰•陽離子交 換層,並以電流密度3 A / d m 2進行電解透析處理,在 pH値達3 · 5時停止透析,而獲得與上述陽離子交換樹 脂處理時略相同的脫鹼氧化矽溶液。 在將具略相同S i 0 2濃度的單純水玻璃水溶液,直接 利用陽離子交換樹脂,將p Η値降至3 · 5左右的處理上 ,需要上述約數倍量的陽離子交換樹脂。此外,離子交換 層法中,亦需要較多的離子交換層數目,同時透析時間上 亦需要長時間。 若將S i 0 2濃度更濃之實施例6的鹼性氧化矽溶液, 利用相同的處理,將p Η値降至3 · 5左右的話,則凝膠 化時間將更早,約爲2 0〜2 4小時左右。該等脫鹼氧化 矽溶液係可作爲本身便具有優越滲透性的地面注入用固結 材。此外,因爲更進一步去除N a離子,所以就環保層面 上而言更佳。 5 ·鹼性氧化矽溶液-酸性反應劑 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) -17 - (請先閱讀背面之注意事項再 裝___ 本頁) 訂: 線· 568946 A7 _B7_ 五、發明說明(15 ) 將表4中實施例2的鹼性氧化矽溶液,與酸性反應劑 的磷酸予以混合,並調整至中性〜酸性區域,結果如表5 示 所 中 (請先閱讀背面之注意事項再 ^—— 本頁) -線· 經濟部智慧財產局員工消費合作社印製 -18- 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 568946 A7 B7 五、發明說明(16 ) 姻 [ΰπΤΡΤΙ 28曰 3.5 3.2 3.0 2.6 2.6 S 酹 駿 獰 ΠΙ CS1 > 寸^1 〇〇 CO cs ro cn — ν (賴尔)(3。0CS1) SE盤^駿· (請先閱讀背面之注意事項再 0L0S71 00CS1〜0001 0寸〜ocn CN1I 〜01 寸·cnre °寸 °°9 •裝___ 本頁: 訂: (r) (r) 0 0 S6A LL 08 2 ςοο 3 it OCSI usi 線- 經濟部智慧財產局員工消費合作社印製Si〇2 (%) 〆, ^ Λ Ah〇3 (%) Fe2〇3 (%) Ca〇 (%) Mg〇 (%) Basic degree hydraulicity Brinell specific surface area (cm2 / g) 31.4 18.6 1.0 46.2 1.3 2.11 0.91 15,000 (7) The sand fine sand system uses Fengpu standard sand, and the silty sand system uses sea sand from Chiba Prefecture, Japan. 2 · Measure (1) Uniaxial compressive strength of sand gel. The sand gel of Fengpu standard sand was hermetically sealed (20 ° C) with polyvinylidene chloride. Printed compression test method for employees' cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs. (2) Gelation time (a) Gel time of homogeneous gel Measured according to the inverted cup method at 20 ° C. (b) The gelation time in the soil is at 20 ° C. After mixing the cement slurry and sand, let it stand, discard the upper clear part, pierce the sand with a bamboo string, and then pull it out. Take the remaining period of the trace as the soil- 13- This paper size is in accordance with Chinese National Standard (CNS) A4 (210 X 297 mm) 568946 A7 B7 V. Gelation time in the description of the invention (11), measure the time. (3) p 値 値 is measured using a glass electrode ρ Η meter. 3. Alkaline silica solution The colloidal silica is mixed with water glass, or the colloidal silica, active silicic acid and water glass are mixed to prepare an alkaline silica solution. The mixing ratio of these compounds, the Si02 concentration in the mixed solution, the amount of Si02 (%) derived from colloidal silica, or the amount of Si02 (%) derived from colloidal silica and activated silicic acid. ), And stability, as shown in Table 4. (Please read the precautions on the back before re-installing this page.) Order ·· · Thread · Printed by the Intellectual Property Bureau Staff Consumer Cooperatives of the Ministry of Economic Affairs This paper is printed in accordance with China National Standard (CNS) A4 (210 X 297 mm) -14-568946 A7 B7 V. Description of the Invention (^) Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs I Alkaline silica solution stability is not gelled, ungelated, ungelated, ungelated, ungelated Ungelatinized Ungelatinized Ungelatinized Ungelatinized Ungelatinized 4 to 5 months later, it was in a semi-gelatinized state. Si02 (%) and 1 1 1 1 21.4 1 Derived from colloidal silica oo 〇〇〇〇〇 〇〇〇 43.9 20.5 28.2 40.7 92.6 1 54.1 Total CN1 1 / S vyS 〇〇r- 〇m cn5 r Ή inch ο 13.9 mixing ratio (per 1000g ) Water (g) ο ON 〇〇〇〇〇〇〇〇〇〇〇〇〇〇 wo ο ι〇νο 〇〇i active silicic acid 1 (g) 1 1 1 instrument 1 1 1 1 1 〇1 1 water glass (g ) m 〇 \ σ \ 〇〇On r—Η 1 fi 1 〇1 〇cn C ^ l cn 1 1 1 〇1 〇CSI 1 ο CO 1 1 1, colloidal silica (g) No · CN1 in Table 1 · Η CN 1 τ—Η 1 1 1 1 1 τ—Η 1 1 Ο 1 1 〇, i 1 cn OQ alkaline silicon oxide solution Comparative Example 1 Comparative Example 2 Example 1 Example 2 Example 3 Example 4 Example 5 Example 6 Example 7 Example 8 Comparative Example 3 (Please read the precautions on the back first and then re-image this page) • Line · This paper size applies the Chinese National Standard (CNS) A4 specification (210 X 297 male) 568946 A7 B7 V. Description of the invention (13) From Table 4, the Si02 concentration in the alkaline silica solution is about 13% as a limit. Below this level, no gelation occurs. Steady state for semi-permanent use. Therefore, these alkaline silica solutions can be stored for a long period of time, and can be disposed of the same as the raw materials of cement slurry, and transferred from the workshop to the site to be injected. In Comparative Example 3, which was 13% or more, it was semi-gelatinized after 4 to 5 months. In addition, in Comparative Example 3, the amount of S i02 derived from colloidal silica also exceeded the range defined by the present invention. When gelation was performed using a reactant, a disadvantage of a relatively slow strength appeared. Therefore, as long as the S i02 concentration is slightly lower than 13%, almost a stable alkaline silica solution can be obtained. In Comparative Examples 1 and 2, the Si02 concentration derived from colloidal silica was 1% or less, and in Comparative Example 1, the total Si02 content was also 3% or less, which all exceeded the limits of the present invention. The range is 値. These, of course, do not cause gelation to be stable. However, as will be described later, the solid obtained with the addition of the reactant will be very soft, and the S 1 02 concentration is about the limit of about 3% '. If it is below this level, the strength will be significantly reduced. Example 7 is an example in which the method is the opposite to that of Example 6 ', and it is an example of stabilization with a large amount of colloidal silica. In Example 8, a small amount of active silicic acid was mixed and stabilized. At this time, the Si02 concentration 'of the active silicic acid in the amount of S102 from the colloidal silica and the active silicic acid was 27 · 8%, which was less than 50%. 4 · Dealkaline silica solution (please read the precautions on the back and then this page) Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs This paper is printed in accordance with China National Standard (CNS) A4 (210x297 mm) -16-568946 A7 B7 Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs. 5. Description of the invention (14) The alkaline silica solution described above is subjected to an alkali-removal treatment using an ion exchange resin or an ion exchange layer to obtain an alkali-repellent silica solution. The alkaline silica solution 5,000 ml obtained in Example 4 of Table 4 was mixed with a cation exchange resin 900 m 1 to obtain an alkali-removing solution of p Η 値 3 · 5 . This de-alkali oxidized sand solution has a Sio2 concentration of 7.1%, and gelation occurs in about 30 to 35 hours. In addition, instead of cation exchange resin treatment, an anion-cation exchange layer was used instead, and electrolytic dialysis treatment was performed at a current density of 3 A / dm 2. Dialysis was stopped when the pH reached 3 · 5 to obtain treatment with the above cation exchange resin. Slightly the same solution of dealkalized silica. In the treatment with a simple water glass aqueous solution having approximately the same S i 0 2 concentration, directly using a cation exchange resin to reduce p 左右 to about 3.5, a cation exchange resin of the above-mentioned several times is required. In addition, in the ion-exchange layer method, a larger number of ion-exchange layers is also required, and a long time is also required for the dialysis time. If the basic silicon oxide solution of Example 6 with a higher concentration of S i 0 2 is used to reduce p Η 値 to about 3.5 by the same treatment, the gelation time will be earlier, about 20 ~ 2 4 hours or so. These alkali-removed silica solutions are used as a ground injection consolidation material with superior permeability. In addition, because the Na ion is further removed, it is better in terms of environmental protection. 5 · Alkaline silica solution-acid reactant The paper size is applicable to the Chinese National Standard (CNS) A4 (210 X 297 mm) -17-(Please read the precautions on the back before reloading this page ___) Order: Line · 568946 A7 _B7_ V. Description of the invention (15) The basic silica solution of Example 2 in Table 4 was mixed with the phosphoric acid of the acidic reactant and adjusted to the neutral to acidic region. The results are shown in Table 5. Medium (Please read the precautions on the back before ^ —— this page) -Line · Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs-18- This paper size applies to China National Standard (CNS) A4 (210 X 297 mm) ) 568946 A7 B7 V. Description of the invention (16) Marriage [ΰπΤΡΤΙ 28, 3.5 3.2 3.0 2.6 2.6 S 酹 Jun 酹 Π CS1 > inch ^ 1 〇CO cs ro cn — ν (Lyre) (3.0CS1) SE Pan ^ Jun. (Please read the precautions on the back before 0L0S71 00CS1 ~ 0001 0 inch ~ ocn CN1I ~ 01 inch · cnre ° inch °° 9 • Installation ___ This page: Order: (r) (r) 0 0 S6A LL 08 2 ςο 3 3 OCSI usi line-Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs

Ln嗽 (r οοοι 驭 dz)^2画 uncnrlf澎黟cn 006 一¾锲 给与嫉iH、纒w丨 ⑺匡辑*發寸嗽 ζ I匡键佩 Π匡辑« 0 I 匡{!!; 6匡辑佩 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) -19- 568946 Α7 Β7 五、發明說明(17) 由表5中得知,本發明固結材料,就凝膠化時間,特 別是可調整爲長時間的凝膠化時間。同樣採用3號水玻璃 ’且S i〇2濃度、p Η値約略相同的實施例1 1 ,1 2, 與比較例4 ( 3號水玻璃-磷酸系)相較下,實施例中磷 酸量非常少,約僅有半量而已。此外,即便凝膠化時間亦 變成非常的長久,強度亦完全毫無遜色的固結體。 6 .鹼性氧化矽溶液-反應劑系、脫鹼氧化矽溶液-反應 劑系 表4中的鹼性氧化矽溶液,除比較例3之外,其餘均 屬無凝膠化的穩定者。可在其中添加反應劑,而使其產生 凝膠化現象。此外,可在脫鹼氧化·矽溶液中添加反應劑, 俾調整凝膠化情形。鹼性氧化矽溶液-反應劑系、與脫鹼 氧化矽溶液-反應劑系之凝膠化時間與固結強度,統籌整 理於表6中。 (請先閲讀背面之注意事項再 I · I I 本頁) 訂· · 經濟部智慧財產局員工消費合作社印製 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) -20 - 568946 A7 B7 五、發明說明(18 )Ln 嗽 (r οοοι 驭 dz) ^ 2 paintings uncnrlf surging cn 006 a ¾ 锲 to give iH, 纒 w 丨 ⑺ 辑 辑 发 寸 嗽 I I 键 佩 佩 匡 匡 «« 0 匡 {!!; 6 Marina The paper size of this paper applies the Chinese National Standard (CNS) A4 specification (210 X 297 mm) -19- 568946 A7 B7 V. Description of the invention (17) It is known from Table 5 that the consolidated material of the present invention is gelled. The gelation time can be adjusted to a long gelation time. In the same way, Example No. 3 and No. 3 water glass were used, and the SiO 2 concentration and p Η 値 were about the same. Compared with Comparative Example 4 (No. 3 water glass-phosphoric acid system), the amount of phosphoric acid in the example was compared. Very few, only about half. In addition, even if the gelation time becomes very long, the strength is completely inferior to the consolidated body. 6. Alkaline silica solution-reactant system, de-alkali silica solution-reactant system Except for Comparative Example 3, the alkaline silica solution in Table 4 is stable without gelation. A reactant can be added to the gelling phenomenon. In addition, a reactant can be added to the alkali-removing and silicon solution to adjust the gelation. The gelation time and consolidation strength of the alkaline silica solution-reactant system and the dealkaliated silica solution-reactant system are summarized in Table 6. (Please read the notes on the back before I. II on this page) Order · · Printed on the paper by the Intellectual Property Bureau Staff Consumer Cooperatives of the Ministry of Economic Affairs The paper size applies to China National Standard (CNS) A4 (210 X 297 mm) -20- 568946 A7 B7 V. Description of the invention (18)

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Kl 4ucn«,φζ* 3 3 ilsm L9l\ 9.e 寸·eπ oo.e 9.S5| 0.S L.i i 9,es 60 SIs re s re 一 Γ9 3 o.e 0.9η OHs 60 ,fo寸 I ^8?scnji Φ8Ι70001 Φ_~s81 ,flR〜urll φοοπος 寸 Φ寸-e Φ8—卜 ^ 0— φ§_ Φ08~Rj ^8°?8/J φι-c 0 mk 〇ς s i 06|mm 〇ςmm os 顚 mi β 08 § sl s (請先閱讀背面之注意事項再@本頁) · · (10001)^¾ αε) 線· 01 ocvl 01 經濟部智慧財產局員工消費合作社印製 (11(1(淫徐 .ON S0 ¾ 〇ς οι 〇ς ςς osl:ef®«sge 00^柴锲给^嫲担繼i_^3qq*fi-寸« 86:髮键&^嘁担盤-Ne匡鎰Ί4-Β-寸« 86:璨铤渣^祕«繼^00匡辑*旮寸« 006:¾¾¾¾祕^纒忉^咳握舾旮寸撇 86:髮锭给安贓繼裝s srnHd脈掛蜮繼 ^ —Kfr ^ i 85燦键给^祕¥邏匡辑M-S-对嗽 006:擦锲&^祕担邏^9匡捶«-5-寸嗽 006:璨鄉§^祕S繼-NH 赵握«-S-寸« 00^柴键&^祕^龜^£匡留»茌寸嗽 006:柴链洽s«ii繼Ne E握fc-fr寸谳 006:柴锲洽^嫲州|、繼^1匡滔«-5-寸« 9iqq «1« oCNMfis^ 2^ 1^ p^ 1^ ^ 1^ s 1^ U匡鎰丑 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) -21 - 568946 A7 B7 五、發明說明(19) 全盤觀察表6 ,凝膠化時間由短時間到長時間均有, 特別是在調整爲較長的凝膠化時間上較爲容易。在源自膠 體氧化矽之S i〇2量偏多的實施例1 4,1 5中,在經過 2天時的強度雖較低,但經過2 8天後,強度便增大頗多 〇 s 1〇2濃度在本發明所界限範圍以下的比較例5,固 結強度極低。另,在本發明所界限範圍以上的比較例6中 ,不管S i 〇2濃度的濃厚與否,並未發見有固結強度的增 加情形,此乃蘊含著固結強度降低的意義。 實施例2 1之脫鹼氧化矽溶液的情況,與具相同程度 之S 1〇2的實施例1 7相比較,雖凝膠化時間明顯拉長, 但強度幾乎無差異。 混入水泥與爐渣的懸浮型實施例(實施例1 6 ,1 8 ,2 0 )中,相較於習知水玻璃一水泥系的比較例8,初 期強度雖稍微差劣,但長期強度卻格外的強化。 S ^〇2濃度比較濃厚的比較例7中,具有凝膠化瞬間 產生,容易產生不均勻固結體的缺點。 7 .凝膠化時間 均質凝膠之凝膠化時間,當然在就防止液化功能上而 言,在土中的凝膠化時間最好可維持較長久的時間。關於 上述表5,6中部分凝膠化時間較長的調配液,係測量在 豐浦標準砂與日本千葉縣海產砂中的凝膠化時間(土中凝 膠化時間)。同時將合倂比較習知顯示較長凝膠化時間之 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) -22 - (請先閱讀背面之注意事項再 丨裝—— I·本頁) .線. 經濟部智慧財產局員工消費合作社印製 568946 A7 _B7_ 五、發明說明(2〇 ) 酸性氧化矽液膠的比較結果,顯示於表7中。 (請先閱讀背面之注意事項再9本頁) 0, 訂·- 線. 經濟部智慧財產局員工消費合作社印製 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) -23 - 568946 A7 B7 五、發明說明(21 ) 經濟部智慧財產局員工消費合作社印製 侧 避 〇 ο ο Ο ο o 〇 〇 ο 寸 ο VO m 〇 o CN ι—Η \ < 寸 VO 髁 1 〇 1" i l l ι ο i ο ι ο l o r—H ^sO vf v〇 Csl ο οο o v〇 οο ι Η CO 1—1 ο οο o 寸 〇 > < ι VO ,^、 舍 If ο ο o Ο ο ο ο o m ο οο o ο ο τ—Η o 卜 CO 寸 ι ON o ο CJ 艇 1 ο ι ο l o ι ο ι ο ο ο i o 寸 l ο ο ο CO o un ο 〇 Η csj ν〇 m τ—Η oo cn un CN Ο o ο 駿 ο Ο o ο ο Ο ο o τ· H 〇 ο ο 獰 ο οο ο (Ν1 o ο οο ο ^Τ) csl ι ? 〇 Csl CN1 ι 鹽 » ι ο ι ο l o ι ο ι ο ο ο o o i o ο ο 獰 ο οο τ—Η υο un ο WO 寸 οο ν i o ι—H wo οο τ—Η 懷 1 If 澎给 擦 璨 璨 燦 S 祕 4π 4Π <Π <Π 4n 4n 〇〇 m • ^tm 鹤 賴 鹤 賴 蚝 Η *Ν cn τ-·__ Η ι i VO r—H ι—Η ON 1 i Csl CNl cn CO m m 匡 匡 μ ϊ 習 m 辑 m ㈣ ㈣ ^祕 u n w u K w u u 發 fr •fr 旮 νο VO 6恢 嗽 嗽 撇 撇 嗽 寸 ν〇 r- oo ON o csl CNl CNl (N (N Oi cn σ\ 匡 冢 匡 m ㈣ 鎰 • 習 習 辑 鎰 U 〇 佩 u 舾 佩 u {U IK jj (請先閱讀背面之注意事項再 —裝---本頁) --線· 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) -24- 568946 Α7 Β7 經濟部智慧財產局員工消費合作社印製 五、發明說明(22) 由表7中得知,雖習知酸性氧化矽溶膠(比較例9的 均質凝膠)顯示非常長的凝膠化時間,但在土中卻明顯的 縮短。尤其是在千葉縣產海砂的情況中更爲明顯。 相對於此,在本發明之實施例2 4〜3 1中’在土中 之凝膠化時間短縮現象極爲微小’仍然保持相當長的凝膠 化時間。供作防止液化用注入材使用而可產生廣範圍滲透 的效果。 8.滲透試驗 由上述試驗結果得知,本發明之地面注入用固結材, 可輕易的進行廣範圍的凝膠化時間調整,尤其是在調整爲 長時間的凝膠化時間上,同時即便在土中亦不致縮短凝膠 化時間,可具備良好的滲透性。爲求慎重起見,採用第1 圖所示實驗用滲透注入試驗裝置,進行滲透試驗。 在第1圖中,透過壓力計2,3,將注入材料6塡充 於連結壓縮機1上且具備有攪拌器4的水槽5中。7係內 徑5 Omm、高度1 · 5m的壓克力製管,在其中將標準 砂8,區分爲9層裝塡,對各層利用水平打擊方式,形成 6 0 %相對密度的緊密度。 接著,塡充於水槽5中的注入材料6,以壓縮機1之 注入壓0 · 5 k g f / c m 2,灌壓管7中的標準砂8。注 入材料便滲透入標準砂8中,觀察滲透距離。第1圖中g ,1 0係切換栓,1 1,1 2係金屬網、1 3係量筒。 試驗中所使用的固結材料與試驗結果,如表8中所示 ^紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) (請先閱讀背面之注意事項再 -fei — 本頁) 訂-· -線. 568946 A7 _B7 五、發明說明(23 。在表8中,滲透試驗Ν ο · 1〜7係本發明之固結材料 ,而滲透試驗N 〇 · 8,9係比較例的固結材料,N 〇 · 8爲超過本發明所界定範圍,而Ν 〇 · 9則爲習知酸性氧 化矽溶膠。 (請先閱讀背面之注意事項再 垂___ 本頁) -線· 經濟部智慧財產局員工消費合作社印製 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) -26- 568946 A7 B7 五、發明說明(24 ) 經濟部智慧財產局員工消費合作社印製 表8 滲透 試驗 No. 使用固結材料 滲透試驗結果 1 表6中實施例13之調配液 標準砂8全長均勻滲透良好之後,並 2 表6中實施例11之調配液 3 表6中實施例17之調配液 4 表6中實施例19之調配液 均勻固結 5 表6中實施例21之調配液 6 表6中實施例22之調配液 7 表6中實施例23之調配液 雖標準砂8全長幾乎有滲透,但由上面起 10cm附近便可發現有不均勻的部分 8 表6中比較例6之調配液 由標準砂8的下面起高約1.0〜1.1m爲止雖 均勻滲透,但以上便呈現不均勻滲透情形 9 Si〇2約5%之pH値2.8的水玻璃-硫酸系酸性氧化矽溶膠 僅由標準砂8的下面起到高度40〜50cm爲 止處有滲透 —— — — — — — — — — — II - I I (請先閱讀背面之注意事項再填寫本頁) 訂-· 線· 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) -27- 568946 A7 B7 五、發明說明(25 ) 由表8中明顯得知,滲透試驗Ν ο · 1〜6的本發明 系統中,橫跨壓克力製管7全長中之標準砂8,均產生滲 透情形,且整體均勻固結。而滲透試驗Ν 〇 · 7雖亦屬本 發明系統,但因水玻璃含量非常多,所以相較於上述滲透 試驗N 〇 . 1〜6下,便略顯遜色。 相對於此,比較例的滲透試驗Ν 〇 . 8雖然充分顯示 出滲透情形,但卻無法完全滲透全長1 . 5 m。換句話說 ,本發明的滲透試驗Ν 〇 . 2相較於比較例的滲透試驗 No.8之下,就均質凝膠化時間而言,不管後者雖然較 爲長久,但滲透性卻反而較差。 此外,比較例的滲透試驗Ν 〇 . 9 ,雖然均質凝膠的 凝膠化時間明顯的長久,但滲透性卻極爲差劣。 由上述足證本發明之固結材料,確實具備極爲優越的 滲透性。 【發明功效】 綜上得知,將膠體氧化矽與水.玻璃,或更加入活性矽 酸,以特定比率混合,製成鹼性氧化矽溶液,再將該鹼性 氧化矽溶液進行脫鹼處理後,便可製得脫鹼氧化矽溶液。 以該脫鹼氧化矽溶液爲基底材料的地面注入用固結材時, 將產生下述功效。 1 ·可調整廣範圍的凝膠化時間,尤其是長時間的凝 膠化時間,且在土中的凝膠化時間亦無短縮現象產生,爲 具備良好滲透性之極佳的防止地面液化用注入固結材料。 (請先閱讀背面之注意事項再_本頁) 士 --線· 經濟部智慧財產局員工消費合作社印製 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) -28 - 568946 A7 ______ B7 五、發明說明(26 ) 2 ·以低氧化矽濃度比率,便,可顯示出較高的固結強 度功效。 3 ·鹼含量較少,具水質環保性佳之功效。 4 ·因爲鹼性氧化矽溶液並非自硬性,所以可由儲存 場所或工廠搬運至注入現場。 5 ·脫鹼氧化矽溶液可利用離子交換樹脂或離子交換 層之柱體等小規模裝置輕易獲得。 6 ·即便使用水泥或爐渣等,亦可均質凝膠,同時可 獲得高強度。 圖式簡單說明】 第1圖係實驗室用注入試驗裝置的槪略圖 圖示符號說明】 (請先閱讀背面之注意事項再 • 4^___ 制本頁: 訂 經濟部智慧財產局員工消費合作社印製 1 壓縮機 2 壓力計 3 壓力計 4 攪拌器 5 水槽 6 固結材料 7 壓克力製管 8 豐浦標準砂 9 切換栓 10 切換栓 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) · 29 - 568946 A7 _B7 五、發明說明(27 )Kl 4ucn «, φζ * 3 3 ilsm L9l \ 9.e inch · eπ oo.e 9.S5 | 0.S Li i 9, es 60 SIs re s re -Γ9 3 oe 0.9η OHs 60, fo inch I ^ 8? Scnji Φ8Ι70001 Φ_ ~ s81, flR ~ urll φοοπος inch Φinch-e Φ8— 卜 ^ 0— φ§_ Φ08 ~ Rj ^ 8 °? 8 / J φι-c 0 mk 〇ς si 06 | mm 〇ςmm os顚 mi β 08 § sl s (Please read the notes on the back before @this page) · · (10001) ^ ¾ αε) Line · 01 ocvl 01 Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs (11 (1 (徐 .ON S0 ¾ 〇 οι 〇ς ς osl: ef® «sge 00 ^ 柴 锲 给 ^ 嫲 继 i_ ^ 3qq * fi-inch« 86: send key & ^ 嘁 tray-Ne Kuang 镒 Ί 4- Β-inch «86: Can slag ^ secret« Follow ^ 00 Kuang Ji * 旮 inch «006: ¾ ¾ ¾ ¾ Secret ^ ^ cough grip 舾 旮 撇 86: send ingots to An Wei JI s srnHd pulse hanging 蜮 JI ^ —Kfr ^ i 85 can key give ^ Secret ¥ Logic Kuang Series MS-On Chou 006: Rubbing & ^ Secret Logic ^ 9 Marina «-5-inch Chou 006: Can Xiang § ^ Secret S-NH Zhao grip «-S-inch« 00 ^ Chai Jian & ^ Secret ^ Turtle ^ £ Kuang Liu »茌 inch cough 006: Chai Chain Qia s« ii following Ne E grip fc-fr inch 谳 006: Chai Qia ^ 嫲State |, Following ^ 1 Marina Tao «-5-inch« 9iqq «1« oCNMfis ^ 2 ^ 1 ^ p ^ 1 ^ ^ 1 ^ s 1 ^ U Kuang Xie This paper is sized to the Chinese National Standard (CNS) A4 (210 X 297 mm) -21-568946 A7 B7 V. Description of the invention (19) Observe Table 6 in its entirety, and the gelation time is from short time to long time It is easy to adjust the gelation time to a long time. In Examples 1 and 15 in which the amount of S iO2 derived from colloidal silica is relatively large, after 2 days, Although the strength was low, after 28 days, the strength increased considerably. Comparative Example 5 whose concentration was below the limit range of the present invention had extremely low consolidation strength. In addition, within the limit range of the present invention In the above Comparative Example 6, no increase in the consolidation strength was observed regardless of the concentration of S i 〇2 or not. This has the meaning of a reduction in the consolidation strength. Example 2 The dealkaliated silica In the case of the solution, compared with Example 17 with the same degree of S 102, although the gelation time was significantly lengthened, the strength was almost the same. Suspension type example mixed with cement and slag (Example 16) , 18, 20), compared with the conventional water glass-cement based comparative example 8, the initial strength is stronger. Although a little poor, but the long-term strength was especially enhanced. Comparative Example 7 having a relatively high S ^ 2 concentration has the disadvantage that gelation occurs instantaneously and uneven consolidated bodies are liable to occur. 7. Gelation time The gelation time of a homogeneous gel, of course, in terms of the function of preventing liquefaction, it is best to maintain the gelation time in the soil for a long time. Regarding some of the formulations with longer gelation times in Tables 5 and 6 above, the gelation time (gelation time in soil) was measured in Toyoura standard sand and marine sand in Chiba, Japan. At the same time, a comparison of conventional papers showing a longer gelation time is applicable to the paper size of China National Standard (CNS) A4 (210 X 297 mm) -22-(Please read the precautions on the back before installing ---- I. This page). Line. Printed by the Consumers ’Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs 568946 A7 _B7_ V. Description of the invention (20) The comparison results of the acidic silica gel are shown in Table 7. (Please read the precautions on the back first and then 9 pages) 0, order ·-line. The paper printed by the Employees' Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs applies the Chinese National Standard (CNS) A4 specification (210 X 297 mm)- 23-568946 A7 B7 V. Description of the invention (21) Avoidance of printing by employees' consumer cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs ο ο Ο ο o 〇〇ο inch VO m 〇o CN ι—Η \ < inchVO 髁 1 〇1 " ill ι ο i ο ι ο lor—H ^ sO vf v〇Csl ο οο ov〇οο ι Η CO 1-1 ο οο o inch 〇 > < ι VO, ^, shed If ο ο o Ο ο ο ο om ο οο o ο ο τ—Η o Bu CO inch ON o ο CJ boat 1 ο ι ο lo ι ο ι ο ο ο io inch l ο ο ο CO o un ο 〇Η csj ν〇m τ —Η oo cn un CN Ο o ο Junο Ο o ο ο ο ο o τ · H 〇ο ο ο ο οο ο (Ν1 o ο οο ο ^ Τ) csl ι? 〇Csl CN1 ι salt »ι ο ι ο lo ι ο ι ο ο ο ooio ο ο 狞 ο οο τ—Η υο un WO Inch οο ν io ι—H wo οο τ—Η Huai 1 If Peng Gongcancancancan S Secret 4π 4Π < Π < Π 4n 4n 〇〇m • ^ tm 赖 赖 鹤 赖 ΗΗ * Ν cn τ -· __ Η ι i VO r—H ι—Η ON 1 i Csl CNl cn CO mm Kuang Kuang μ 习 m series m ㈣ ^ ^^ unwu K wuu hair fr • fr 旮 νο VO 6 Inch ν〇r- oo ON o csl CNl CNl (N (N Oi cn σ \ 匡 丘 匡 m ㈣ • 习 修 镒 U 〇 佩 u 舾 佩 u {U IK jj (Please read the precautions on the back before— (Installation --- this page) --- line · This paper size applies to China National Standard (CNS) A4 (210 X 297 mm) -24- 568946 Α7 Β7 Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs (22) As can be seen from Table 7, although the conventional acidic silica sol (homogeneous gel of Comparative Example 9) showed a very long gelation time, it was significantly shortened in the soil. Especially in the case of sea sand produced in Chiba Prefecture. On the other hand, in Examples 2 4 to 31 of the present invention, the 'shortening phenomenon of the gelation time in the soil is extremely small' and the gelation time is still kept long. It is used as an injection material to prevent liquefaction and has a wide range of penetration effects. 8. Penetration test It is known from the test results that the consolidation material for floor injection of the present invention can easily adjust a wide range of gelation time, especially when it is adjusted to a long time gelation time. It does not shorten the gelation time in the soil and can have good permeability. For the sake of caution, the permeation test was performed using the experimental permeation injection test apparatus shown in Figure 1. In Fig. 1, the injection material 65 is filled in a water tank 5 having a stirrer 4 connected to the compressor 1 through the pressure gauges 2, 3. The 7 series acrylic pipe with an inner diameter of 5 Omm and a height of 1.5 m is used to divide the standard sand 8 into 9 layers of decoration. The horizontal strike method is used for each layer to form a compactness of 60% relative density. Next, the injection material 6 filled in the water tank 5 is filled with the standard sand 8 in the pressure pipe 7 at an injection pressure of 0.5 kgf / cm2 of the compressor 1. The injected material penetrates into the standard sand 8 and observes the penetration distance. In the first figure, g, 10 series switching plugs, 1 1, 12 series metal nets, and 13 series measuring cylinders. The consolidation materials and test results used in the test are as shown in Table 8. ^ The paper size applies the Chinese National Standard (CNS) A4 specification (210 X 297 mm) (Please read the precautions on the back before -fei — this Page) Order-·-Line. 568946 A7 _B7 V. Description of the invention (23. In Table 8, the penetration test N ο · 1 ~ 7 is the consolidation material of the present invention, and the penetration test N 〇 8, 9 is compared As an example of the consolidation material, No. 8 is beyond the scope defined by the present invention, and No. 9 is the conventional acidic silica sol. (Please read the precautions on the back before hanging on this page)-Line · Printed by the Intellectual Property Bureau of the Ministry of Economic Affairs, Consumer Cooperatives The paper size is applicable to the Chinese National Standard (CNS) A4 specification (210 X 297 mm) -26- 568946 A7 B7 V. Description of the invention (24) Employee Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs Printed Table 8 Penetration Test No. Penetration Test Results with Consolidation Material 1 The standard liquid 8 of the preparation liquid of Example 13 in Table 6 is uniformly penetrated throughout the entire length, and 2 is the preparation liquid of Example 11 in Table 6 3 and implemented in Table 6 Preparation solution 4 of Example 17 Preparation of Example 19 in Table 6 The liquid is uniformly consolidated 5 The liquid preparation of Example 21 in Table 6 6 The liquid preparation of Example 22 in Table 6 7 The liquid preparation of Example 23 in Table 6 Although the standard sand 8 has almost full penetration, it is about 10 cm from the top It can be found that there is an uneven portion 8 The mixing solution of Comparative Example 6 in Table 6 is uniformly penetrated from the bottom of the standard sand 8 to a height of about 1.0 to 1.1 m, but the above shows uneven penetration 9 Si〇2 about 5 Percentage of water glass-sulfuric acid-based silica sol with a pH of 2.8 only penetrates from the bottom of the standard sand 8 to a height of 40 ~ 50cm —— — — — — — — — — — II-II (Please read first Note on the back page, please fill in this page again) Order-· Thread · This paper size is applicable to China National Standard (CNS) A4 (210 X 297 mm) -27- 568946 A7 B7 V. Description of the invention (25) From Table 8 It is clearly known that in the system of the present invention of the penetration test Ν ο 1 to 6, the standard sand 8 across the entire length of the acrylic pipe 7 all produced a penetration situation, and the whole was uniformly consolidated. The penetration test Ν 〇 · 7Also belongs to the system of the present invention, but due to the very large content of water glass, It was slightly inferior to the above penetration test No. 0.1 to 6. In contrast, although the penetration test No. 0.8 of the comparative example fully showed the penetration situation, it could not completely penetrate the entire length of 1.5 m. In other words In other words, the permeation test No. 2 of the present invention is lower than the permeation test No. 8 of the comparative example in terms of homogeneous gelation time, but the permeation is inferior in spite of the fact that the latter is relatively long. In addition, in the permeation test No. 9 of the comparative example, although the gelation time of the homogeneous gel was remarkably long, the permeability was extremely poor. The above-mentioned evidence confirms that the consolidation material of the present invention has extremely superior permeability. [Effect of the invention] In summary, it is known that colloidal silica and water, glass, or active silicic acid are added, mixed at a specific ratio to make an alkaline silica solution, and the alkaline silica solution is dealkaliated. After that, a dealkaliated silica solution can be prepared. The following effects are produced when the consolidation material for floor injection uses the dealkaliated silica solution as a base material. 1 · The gelation time can be adjusted in a wide range, especially for a long time, and there is no shrinkage in the gelation time in the soil. Inject consolidation material. (Please read the precautions on the back first_page) Taxi-line · Printed by the Intellectual Property Bureau of the Ministry of Economic Affairs, Consumer Cooperatives This paper is printed in accordance with Chinese National Standard (CNS) A4 (210 X 297 mm) -28- 568946 A7 ______ B7 V. Description of the invention (26) 2 · With low silicon oxide concentration ratio, it can show higher consolidation strength effect. 3. Less alkali content, it has the effect of good water quality and environmental protection. 4 · Since the alkaline silica solution is not self-hardening, it can be transported from the storage place or factory to the injection site. 5 · The alkali-removing silica solution can be easily obtained by using a small-scale device such as an ion exchange resin or a column of an ion exchange layer. 6 · Even if cement or slag is used, the gel can be homogenized and high strength can be obtained. Brief description of the diagram] Figure 1 is a schematic diagram of the injection test device used in the laboratory. [Please read the precautions on the back first. 4 ^ ___ Make this page: Order by the Intellectual Property Bureau, Ministry of Economic Affairs, Consumer Consumption Cooperatives System 1 Compressor 2 Pressure gauge 3 Pressure gauge 4 Agitator 5 Water tank 6 Consolidation material 7 Acrylic tube 8 Fengpu standard sand 9 Switching bolt 10 Switching bolt This paper applies the Chinese National Standard (CNS) A4 specification (210 X 297 mm) · 29-568946 A7 _B7 V. Description of the invention (27)

3 IX 筒量 (請先閱讀背面之注意事項再 ,¾—— 本頁) 線. 經濟部智慧財產局員工消費合作社印製 11 金屬網 1 2 金屬網 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) -30 -3 IX tube weight (please read the precautions on the back first, ¾—— this page) line. Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs. 11 Metal mesh 1 2 Metal mesh This paper applies Chinese National Standard (CNS) A4 Specifications (210 X 297 mm) -30-

Claims (1)

56894ά^ IΚ告本 六、申請專利範圍 第89124686號專利申請案 中文申請專利範圍修正本 民國91年11月21日修正 1. 一種地面注入用固結材,其特徵在於:由含有膠 體氧化矽與水玻璃,且在注入地面之前,本身並不產生凝 膠化的鹼性氧化矽溶液所組成者。 2. —種地面注入用固結材,其特徵在於:含有膠體 氧化矽與水玻璃的鹼性氧化矽溶液,其中該溶液中的 S i 〇2濃度爲3〜1 3重量%,而源自膠體氧化矽中的 S i〇2量則爲1〜5 0重量%。 3 . —種地面注入用固結材,其特徵在於··其爲含有 膠體氧化矽、水玻璃與活性矽酸的鹼性氧化矽溶液,其中 該溶液中的S i〇2濃度爲3〜1 3重量%,而源自膠體氧 化矽與活性矽酸中的S i〇2量則爲1〜5 0重量%。 4 ·如申請專利範圍第1〜3項中任一項所述之地面 注入用固結材’係爲將該鹼性氧化矽溶液進行脫鹼處理的 脫鹼氧化矽溶液者。 5 ·如申請專利範圍第1〜3項中任一項所述之地面 注入用固結材,更進一步調配有反應劑。 6 ·如申請專利範圍第4項所述之地面注入用固結材 ,更進一步調配有反應劑。 7 ·如申請專利範圍第5項所述之地面注入用固結材 ,其中該反應劑係選擇自酸性反應劑、無機鹽類、水泥、 本紙張尺度適用中國國家梂準(CNS ) A4規格(210X297公釐) — (請先閲讀背面之注意事項再填寫本頁) 訂 經濟部智慧財產局員工消費合作社印製 568946 A8 B8 C8 D8 、申請專利範圍 及爐渣中者。 8 .如申請專利範圍第6項所述之地面注入用固結材 泥 水 類 鹽 機 無 劑 應 反 性 酸 白 擇 選 係 劑 應。 反者 該中 中渣 其爐 , 及 (請先閲讀背面之注意事項再填寫本頁) 經濟部智慧財產局員工消費合作社印製 -2- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐)56894ά ^ IKK Notice VI. Patent Application No. 89124686 Chinese Patent Application Amendment Amendment November 21, 1991 1. A consolidation material for ground injection, which is characterized in that it consists of colloidal silicon oxide and Water glass, which does not itself produce a gelled alkaline silica solution before being injected into the ground. 2. A consolidation material for ground injection, which is characterized by an alkaline silica solution containing colloidal silica and water glass, wherein the S i 〇2 concentration in the solution is 3 to 13% by weight, and is derived from The amount of Si02 in the colloidal silica is 1 to 50% by weight. 3. A consolidation material for ground injection, characterized in that it is an alkaline silica solution containing colloidal silica, water glass and active silicic acid, wherein the S i02 concentration in the solution is 3 to 1 3% by weight, and the amount of Si02 derived from colloidal silica and active silicic acid is 1 to 50% by weight. 4 · The consolidation material for floor injection as described in any one of the items 1 to 3 of the scope of the patent application is a dealkaliated silica solution that is subjected to a dealkaliating treatment of the alkali silica solution. 5 · According to any one of items 1 to 3 of the scope of patent application, the ground injection consolidating material is further prepared with a reactant. 6 · The ground-injection consolidation material as described in item 4 of the scope of patent application, and further deployed with a reagent. 7 · Consolidation material for ground injection as described in item 5 of the scope of the patent application, where the reactant is selected from acid reactants, inorganic salts, cement, and this paper is applicable to China National Standard (CNS) A4 specifications ( 210X297 mm) — (Please read the notes on the back before filling this page) Order the printed 568946 A8 B8 C8 D8 by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs, the scope of the patent application and the slag. 8. As described in Item 6 of the scope of the patent application, the cement-free salt water machine for ground injection should be used as a non-reactive acid white selection agent. The opposite is the one in China and China, and (please read the notes on the back before filling this page) Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs -2- This paper size applies to China National Standard (CNS) A4 (210X297 Mm)
TW89124686A 1999-06-21 2000-11-21 Grouting consolidation material TW568946B (en)

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US7163358B2 (en) 2002-08-22 2007-01-16 Akzo Nobel N.V. Injection grouting
ES2347238T3 (en) * 2002-08-22 2010-10-27 Akzo Nobel N.V. MILK BY INJECTION.
JP2007314724A (en) * 2006-05-29 2007-12-06 Raito Kogyo Co Ltd Material for soil improvement
JP5578642B2 (en) * 2007-12-28 2014-08-27 強化土エンジニヤリング株式会社 Ground injection agent and ground injection method
JP4696200B2 (en) * 2009-02-12 2011-06-08 強化土株式会社 Ground injection method
JP6051419B2 (en) * 2012-09-24 2016-12-27 富士化学株式会社 Ground injection solidification material in which elution of sulfate ions to the ground is suppressed, and ground injection construction method using the same
JP6233818B2 (en) * 2016-03-28 2017-11-22 富士化学株式会社 Method for producing consolidated material for ground injection
JP7355358B2 (en) * 2017-06-19 2023-10-03 富士化学株式会社 Consolidation material for ground injection and its manufacturing method
JP6608024B1 (en) * 2018-10-29 2019-11-20 強化土エンジニヤリング株式会社 Ground injection material and ground improvement method
JP7299869B2 (en) * 2020-02-14 2023-06-28 花王株式会社 Ground improvement method

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