The invention relates to a method of preparing a ground injection material and the injection material to be used in permeation injections of dams, tunnel constructions, permanent and temporary deep excavations, rock fissures, and soils up to silt size that cannot be injected with cement injections within the scope of geotechnical engineering.
Many injection materials are used in permeation injection applications. Portland cements are one of the most used injection materials, but due to their large particle sizes, it is difficult for them to penetrate into the fine and medium sand samples and it is hard to adjust their setting times. For this reason, new injection materials that could penetrate smaller particle sizes were needed. With the development of the chemical injection material, injection into smaller particle sizes has become possible, but the application areas have been limited due to their low strength, high costs, and negative effects on the environment. Hence, there is a need for an environmentally friendly injection material that can provide high strength and low permeability after injection with an adjustable gelling time.
In the scope of the known technique, this material is frequently used in injection applications to prevent such problems. The injection material used in injection applications mostly consists of sodium silicate based materials. In this application, silicate-based materials are neutralized and gelled using a reactant. Many weak acid type materials are used as reactants for this process. These acids are expensive and difficult to supply.
The purpose of permeation injection applications is to ensure that the solution material reaches the soils pores in a timely manner and to gelate after reaching them. During very long gelling times, especially in areas with groundwater, the solution is diluted and gelling cannot be achieved.
Document no. KR101697964B1 discloses a low-cost injection material produced by using recycled resources. The composition comprises a gelling agent containing sodium silicate and binding element mixed with the gelling agent to form a gel type accelerator.
As a result, all issues mentioned above made it necessary to make an innovation in the relevant technical field.
This invention aims to overcome the above-mentioned problems and make a technical innovation in the relevant field.
The main object of the invention is to develop an environmentally friendly injection material to be used in permeation injections of dam soils, tunnel constructions, permanent and temporary deep excavations, rock fissures, and soils up to silt size that cannot be injected with cement injections within the scope of geotechnical engineering.
Another object of the invention is to develop a method for the use of environmentally friendly ultra low sulfate boric acid in soil injection materials and to adjust the gelling time for this use.
Another object of the invention is to increase the strength and decrease the permeability in the soils after injection.
Another object of the invention is to make permeation injection easily to the soil up to silt size.
Another object of the invention is to facilitate control of the pH of the medium by controlling the concentration of ultra low sulfate boric acid and to adjust the gelling time of the solidified material to be formed accordingly.
Another object of the invention is to provide easy injection opportunity even in the flowing groundwater conditions.
Another object of the invention is to ensure the injection to reach the soil pores in a timely manner and to gelate after reaching it. The desired gelling times can be easily adjusted with the developed product.
Another object of the invention is to provide an environmentally friendly injection material.
This invention is a method for preparing a material to be applied in the form of permeation injection in soils up to the size of silt, in order to achieve all the objectives mentioned above and included in the detailed description below. Accordingly, the method presented within the scope of the invention includes the following steps: Preparing a mixture of sodium silicate and water provided with a SiO2/Na2O ratio of 3-4, so that their ratio by volume varies between 3/7 and 1/1; Obtaining a mixture by dissolving ultra low sulfated boric acid in water, containing ultra low sulfated boric acid between 2.5-5% by weight; Mixing the resulting ultra low sulfate boric acid-water mixture with sodium silicate obtained in the first step.
In a preferred embodiment of the invention, the sodium silicate SiO2/Na2O ratio is 3.2.
In a preferred embodiment of the invention, the ultra-low sulfated boric acid ratio added to water is increased to reduce gelling time or decreased to increase gelling time.
In order to achieve all the objectives mentioned above and included in the following detailed description, the invention is an injection material obtained by the method according to any one of claims 1-4, which reinforces the soil by settling in said pores in the soil up to silt size by being injected into the pores in the soil.
In this detailed description, a method for preparing an injection material according to the invention and the injection material obtained are described only with examples that will not have any limiting effect in order to better understand the subject.
The subject of the invention is related to the method for the preparation of materials for the geotechnical engineering, where cement mixtures are insufficient, and the construction of dam soils, tunnel constructions, permanent and temporary deep excavations, rock fissures, and permeation injections up to silt size.
In the method of the invention, it is explained how to control the gelling time with the use of ultra low sulfate boric acid. Here, the expression “ultra low sulphate boric acid” is limited to boric acids containing sulphate at a maximum rate of 3 ppm.
Sodium silicates, known as water glass, are prepared by heating silicate sand or silica of any form with Na2CO3 at around 900° C. After refining, sodium silicate becomes a fluid solution. This solution can be diluted with water to obtain the concentration that meets the need. Sodium silicate is neutralized and gelled using a weak acid or salt acid as a reactant.
In order for sodium silicates to be used as the injection material described in the invention, it is essential that the silica/alkali ratios (SiO2/Na2O) are between 3 and 4. In a preferred embodiment, this ratio is 3.2.
Organic or inorganic reactants are used in the gelling process of sodium silicates. In this invention, sodium silicate and ultra-low sulfated boric acid of inorganic origin are used. Ultra low sulphate boric acid is dissolved by mixing in water in the mixtures and then mixed with sodium silicate in certain proportions. Sodium silicate and ultra low sulfate materials are mixed and the following reaction occurs.
According to the reaction equation, when sodium silicate, which is alkaline in nature, is diluted, it ionizes by hydrolysing in aqueous medium. Na+ cations and tetrahedral silica chains are surrounded by H2 molecules. When an aqueous ultra low sulfate boric acid solution with concentrated concentrate is added on this alkaline solution, it gradually enters the sodium silicate chains of the polymeric chain structure, which is in the form of a polymeric chain, and draws the pH of the environment towards neutral levels.
When the ambient pH is neutral, the polymeric sodium borosilicate structure proposed by the products in the above reaction begins to form and mechanical setting occurs accordingly.
When a trigonal structure ultra low sulfate boric acid aqueous solution is prepared, it turns into a tetragonal (a geometry similar to silicate structure) with hydrolysis, which facilitates the formation of a silicate-like chain to enter among polymeric silicate derivatives. The tetragonal borate structure in anionic character increases the stability of the hard material formed by balancing its charge with the cationic Na+ atoms in the sodium silicate structure.
The reaction that takes place between sodium silicate chains and tetragonal borate anions is a kind of esterification reaction, which is carried out through H2O elimination. As a result of the reaction described above, the solution gelates.
48 different injections of 100 ml prepared with the inputs in the range given in Table 1 and their gelling times are shown. Here, ultra-low sulphate boric acid is mixed with sodium silicate by using a magnetic stirrer.
As can be seen in Table 1 examples B1-B7, while the amounts of water and sodium silicate have been steadily provided, the gelling time of the injection increases regularly as the amount of ultra-low sulfated boric acid decreases.
In addition, as can be seen in B8, B23, and B31, the amount of ultra-low sulphate boric acid is kept constant by mass, and the gelling time increases when the volume of water is increased compared to sodium silica. In contrast, when the ratio of sodium silicate to volume increases, gelling time decreases.
Strength and Permeability Values Obtained by the Said Injection;
By injection, the unconfined compressive strength of sand samples can be up to 0.50 MPa and the unconfined compressive strength of silt samples can be up to 0.30 MPa. Also, with the developed injection, the permeability coefficients of sand samples decrease to 1×10−6 cm/sec and the permeability coefficients of silt samples to 1×10−7 cm/sec.
The scope of the protection of the invention is set forth in the annexed claims and certainly cannot be limited to exemplary explanations in this detailed description. It is evident that one skilled in the technique can make similar embodiments in the light of the explanations above without moving away from the main theme of the invention.
Filing Document | Filing Date | Country | Kind |
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PCT/TR2020/050339 | 4/22/2020 | WO |
Publishing Document | Publishing Date | Country | Kind |
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WO2020/236107 | 11/26/2020 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
3663249 | Rao | May 1972 | A |
3884839 | Bon | May 1975 | A |
4194918 | George | Mar 1980 | A |
4203773 | Temple | May 1980 | A |
4329177 | George | May 1982 | A |
4396723 | Temple | Aug 1983 | A |
5084260 | Bertocci | Jan 1992 | A |
5246654 | Ertle | Sep 1993 | A |
5501826 | Ertle | Mar 1996 | A |
20090230352 | Gimvang | Sep 2009 | A1 |
20200407233 | Yakar Elbeyli | Dec 2020 | A1 |
Number | Date | Country |
---|---|---|
H1036842 | Feb 1998 | JP |
20090022342 | Mar 2009 | KR |
101697964 | Jan 2017 | KR |
2009015520 | Feb 2009 | WO |
Entry |
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International Search Report for corresponding PCT/TR2020/050339, dated Aug. 26, 2020. |
Written Opinion of the International Searching Authority for corresponding PCT/TR2020/050339, dated Aug. 26, 2020. |
Number | Date | Country | |
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20220212997 A1 | Jul 2022 | US |