Effect of inorganic salt impurities on seeded precipitation of silica hydrate from sodium silicate solution

To clarify the precipitation of silica hydrate from the real desilication solutions of aluminosilicate solid wastes by adding seeds and improve integrated waste utilization,the seeded precipitation was studied using synthesized sodium silicate solution containing different inorganic salt impurities.The results show that sodium chloride,sodium sulfate,sodium carbonate,or calcium chloride can change the siloxy group structure.The number of high-polymeric siloxy groups decreases with increasing sodium chloride or sodium sulfate concentration,which is detrimental to seeded precipitation.Calcium chloride favors the polymerization of silicate ions,and even the chain groups precipitate with the precipitation of high-polymeric sheet and cage-like siloxy groups.The introduced sodium cations in sodium carbonate render a more open network structure of high-polymeric siloxy groups,although the carbonate ions favor the polymerization of siloxy groups.No matter how the four impurities affect the siloxy group structure,the precipitates are always amorphous opal-A silica hydrate.

Effectiveness of Sodium Silicate on the Corrosion Protection of AA7075-T6 Aluminium Alloy in Sodium Chloride Solution

The influence of sodium silicate on the corrosion behaviour of aluminium alloy 7075-T6 in 0.1 M sodium chloride solution was studied by open circuit potential (OCP) and electrochemical impedance spectroscopy (EIS) techniques. Scanning electron microscopy (SEM) was used to characterize the AA7075-T6 surface. Silicate can significantly reduce corrosion deterioration and the inhibition efficiency increases with the concentration of Na2SiO3. The corrosion inhibition mechanism involves the formation of a protective film over the alloy surface by adsorption of aluminosilicate anions from solution, as has also been suggested by others in literature.

Adsorption of sodium polyacrylate at interface of dicalcium silicate-sodium aluminate solution

The adsorption isotherm of sodium polyacrylate on dicalcium silicate（2CaO-SiO2） in sodium aluminate solution at 80 ℃ was studied.The type of surface adsorption of sodium polyacrylate is saturated adsorption,and the adsorption behavior belongs to L-type,according with the monolayer adsorption model of Langmuir equation.The surface coverage of sodium polyacrylate is 1.06 mol/μm2.The relation curve between the surface pressure and the molecular area of adsorption film was obtained by Gibbs formula.The variation of interfacial energy caused by adsorption as well as the relationship between the relation curve and the type of adsorption was discussed.

Influence of sodium silicate on manganese electrodeposition in sulfate solution

The influences of sodium silicate on manganese electrodeposition in sulfate solution were investigated. Manganese electrodeposition experiments indicate that a certain amount of sodium silicate can improve cathode current efficiency and initial pH 7.0?8.0 is the optimized pH for high cathode current efficiency. The analyses of scanning electron microscopy (SEM) and X-ray diffraction (XRD) indicate the compact morphology and nanocrystalline structure of electrodeposits. X-ray photoelectron spectrometry (XPS) analysis shows that the elements of Mn, Si and O exist in the deposit. The solution chemistry calculations of sulfate electrolyte and sodium silicate solution indicate that species of Mn2+, MnSO4, Mn(SO4)2?2 , Mn2+, MnSiO3, Mn(NH3)2+, SiO32?and HSiO3? are the main active species during the process of manganese electrodeposition. The reaction trend between Mn2+ and Si-containing ions is confirmed by the thermodynamic analysis. In addition, polarization curve tests confirm that sodium silicate can increase the overpotential of hydrogen evolution reaction, and then indirectly improve the cathode current efficiency.

Electrochemical mechanism and flotation of chalcopyrite and galena in the presence of sodium silicate and sodium sulfite

The electrochemical mechanism involved in the selective separation of chalcopyrite from galena was investigated by flotation and electrochemical methods in the presence of sodium sulfite and sodium silicate,respectively,as a single depressant and their mixture as a combined depressant.Flotation tests revealed that the floatability of chalcopyrite was unaffected by depressants and its recovery remained constant(>80%)within the studied dosage range.Galena flotation was severely depressed with descending depressing order as follows:combined depressant﹥sodium silicate﹥sodium sulfite.Electrochemical analysis confirmed the high affinity of depressants on the galena surface,resulting in the formation of hydrophilic species,such as lead sulfite,lead sulfate,and lead orthosilicate.The oxidation of chalcopyrite surface and depressants did not exhibit any signals;conversely,the self-oxidation of chalcopyrite was depressed.The results of cyclic voltammograms well agreed with flotation results,demonstrating that chalcopyrite primarily reacted with the collector O-isopropyl-N-ethyl thionocarbamate and that galena mostly reacted with depressants.

Dry reusing and wet reclaiming of used sodium silicate sand

Based on the characteristics of used sodium silicate sand and the different use requirements for recycled sand, "dry reusing and wet reclaiming of used sodium silicate sand" is considered as the most suitable technique for the used sand. When the recycled sand is used as support sand, the used sand is only reused by dry process including breaking, screening, dust-removal, etc., and it is not necessary that the used sand is reclaimed with strongly rubbing and scraping method, but when the recycled sand is used as facing sand (or single sand), the used sand must be reclaimed by wet method for higher removal rate of the residual binders. The characteristics and the properties of the dry reused sand are compared with the wet reclaimed sand after combining the different use requirements of support sand and facing sand (or single sand), and above the most adaptive scheme has also been validated.

The effect of sodium silicate concentration on microstructure and corrosion properties of MAO-coated magnesium alloy AZ31 in simulated body fluid

In recent years,magnesium and its alloys are considered as biodegradable implants.However magnesium implants may rapidly corrode before the natural healing process of the tissue is completed.In this investigation,micro arc oxidation process has been studied for avoiding primary corrosion of the magnesium alloy in simulated body fluid.Anodized coating was formed on AZ31 alloy in nontoxic silicate-alkaline solution at constant current.The effects of silicate concentration and conductivity of electrolyte solution on microstructure and corrosion properties of coating were evaluated.Scanning electron microscopy showed that a thick and condensed coating is formed after enough anodizing period.Energy dispersive spectroscopy showed that Si,O and Mg are the main components of the coating.Corrosion resistance of the coated and uncoated samples was assessed using potentiodynamic polarization and electrochemical impedance spectroscopy tests in SBF at 37℃ and pH of 7.4.Maximum corrosion resistance was achieved at 30 g/L concentration of sodium silicate in anodizing solution.It was observed that further increase in silicate concentration decreased the corrosion resistance.

Wet reclamation of sodium silicate used sand and biological treatment of its wastewater by Nitzschia palea

The massive amount of sodium silicate in the used sand was a pollution source, especially in the waste water from the wet reclamation of used sand. A new process of wet reclamation by biologically treating the waste water produced during the wet reclamation process of used sand was studied in the paper. In the work, the precultivation of N. palea was performed firstly, and three different scrubbing solutions： （1） tap water, （2） modified medium for N. palea, and （3） filtrate of the broth treated by N. palea for 15 days, were used. The results of the primary investigation show that a de-skinning ratio of 90% is obtained when using the scrubbing solution containing modified medium for N. palea at the ratio 1：2 of sand and scrubbing solution, and the maximal concentrations of Na^＋ and SiO3^2- are 1.49 g.L-1 and 0.51 g.L-1, respectively. The results of the optimal biomass, pH value decrease and Na^＋ and SiO32 consumption indicate the optimal incubation conditions are at the irradiance of 5,000 lux and 25 ℃. Using the filtrate of the broth treated by N. palea for 15 days as the scrubbing solution directly, a de-skinning ratio of 93% is the highest compared to the results of the tap water and the modified medium for N. palea. In the biological process using N. palea, less water is used and little wastewater is produced, which is advantageous to the purpose of green manufacturing and environmental protection.

Cementing properties of steel slag activated by sodium silicates and sodium hydroxide

Steel slag which is mainly composed of γ-Ca2SiO4 and other silicates or alumino-silicates is activated by sodium sificates and sodium hydroxide. The powders of such steel slag are usually inert to hydrate and subsequently have very low ability of cementing. But when sodium silicates and sodium hydroxide are used as activators the steel slag shows very good properties of cementing. When activated with NaOH solution the hardened slurry of the steel slag has a compressive strength of 11.13 MPa after being cured for 28 days. When activated with Na2SiO3 solution the samples after being cured for 28 days have an average compres- sive strength of 40.23 MPa. While the steel slag slurry which is only mixed with water has a compressive of 0.88 MPa after being cured for 28 days.

Evaluation of the effect of sodium silicate addition to mine backfill,Gelfill-Part 2:Effects of mixing time and curing temperature

The effects of mixing time and curing temperature on the uniaxial compressive strength （UCS） andmicrostructure of cemented hydraulic fill （CHF） and sodium silicate-fortified backfill （Gelfill） wereinvestigated in the laboratory. A series of CHF and Gelfill samples was mixed for time periods rangingfrom 5 min to 60 min and cured at temperatures ranging from 5 C to 50 C for 7 d, 14 d or 28 d.Increasing the mixing time negatively influenced the UCS of Gelfill samples, but did not have a detectableeffect on CHF samples. The curing temperature had a strong positive impact on the UCSs of both Gelfilland CHF. An elevated temperature caused rapid UCS development over the first 14 d of curing. Mercuryintrusion porosimetry （MIP） indicated that the pore size distribution and total porosity of Gelfill werealtered by curing temperature.

Effectiveness of sodium silicate as gangue depressants in iron ore slimes flotation

The recovery of iron from the screw classifier overflow slimes by direct flotation was studied. The relative effectiveness of sodium silicates with different silica-to-soda mole ratios as depressants for silica and silicate bearing minerals was investigated. Silica-to-soda mole ratio and silicate dosage were found to have significant effect on the separation efficiency. The results show that an increase of Fe content in the concentrate is observed with concomitant reduction in SiO2 and A1203 levels when a particular type of sodium silicate at a proper dosage is used. The concentrate of 58.89wt% Fe, 4.68wt% SiO2, and 5.28wt% A1203 with the weight recovery of 38.74% and the metal recovery of 41.13% can be obtained from the iron ore slimes with 54.44wt% Fe, 6.72wt% SiO2, and 6.80wt% A1203, when NazSiO3 with a silica-to-soda mole ratio of 2.19 is used as a depressant at a feed rate of 0.2 kg/t.

Properties of sodium silicate bonded sand hardened by microwave heating

The sodium silicate bonded sand hardened by microwave heating has many advantages,such as low sodium silicate adding quantity,fast hardening speed,high room temperature strength,good collapsibility and certain surface stability.However,it has big moisture absorbability in the air,which would lead to the compression strength and the surface stability of the sand molds being sharply reduced.In this study,the moisture absorbability of the sodium silicate bonded sand hardened by microwave heating in different humidity conditions and the effect factors were investigated.Meanwhile,the reasons for the big moisture absorbability of the sand were analyzed.Some measures to overcome the problems of high moisture absorbability,bad surface stability and sharply reducing strength in the air were discussed.The results of this study establish the foundation of green and clean foundry technology based on the microwave heating hardening sodium silicate sand process.

An improved sodium silicate binder modified by ultra-fine powder materials

This paper presents a new method of modifying sodium silicate binder with ultra-fine powders. The sodium silicate binder modified by ultra-fine powder A and the organic B can reduce the addition amount of the binder. The results indicate that the 24 h strength has increased by 39.9% at room temperature and the residual strength has decreased by 30.7% at 800℃, compared to the conventional sodium silicate. An available material to improve the moisture resistance was also found by adding about 2% more inorganic C, and it can increase the moist strength by 20%. In the end, the microanalyses are given to explain the modifying machanism, i. e., the ultra-fine powder A can refine the sodium silicate binder to avoid holes in the binder bond, which can increase the 24 h strength at room temperture, and can lead to more cracks in the bond after the molding sand is heated to 800℃. This is because of the stress caused by the new eutectic complex of modified sodium silicate binder.

Influence of silicate anions structure on desilication in silicate-bearing sodium aluminate solution

The structural changes of silicate anions in the desilication process with the addition of calcium hydrate alumino-carbonate were studied by measuring Raman spectra, infrared spectra and corresponding second derivative spectra. The results show that the desilication ratio in the solution prepared by the addition of sodium silicate(solution-SS) is much greater than that in the solution by the addition of green liquor(solution-GL), and low alumina concentration in the sodium aluminate solutions facilitates the desilication process. It is also shown that alumino-silicate anions in the solution-GL, and Q^3 polymeric silicate anions in solution-SS are predominant, respectively. In addition, increasing the concentration of silica favors respectively the formation of the alumino-silicate or the Q^3 silicate anions in the solution-GL or the solution-SS. Therefore, it can be inferred that the low desilication ratio in the silicate-bearing aluminate solution is mainly attributed to the existence of alumino-silicate anions.

Determination of Iron in Layered Crystal Sodium Disilicate and Sodium Silicate by Flame Atomic Absorption Spectrometry with Boric Acid as a Matrix Modifier

The effects of matrix silicate and experimental conditions on the determination of iron in flame atomic absorption spectrometry （FAAS） were investigated. It was found that boric acid as a matrix modifier obviously eliminated silicate interference. Under the optimum operating conditions, the determination results of iron in layered crystal sodium disilicate and sodium silicate samples by FAAS were satisfactory. The linear range of calibration curve is 0-10.5 μg.mL^-1, the relative standard deviation of method is 1.2%-2.2%, the recovery of added iron is 96.0%- 101%, the sensitivity is 0.19 μg.mL^-l and the detection limit is 77 ng.mL^-1. The effect of the determination of iron of the standard curve method, standard addition calibration and colorimetry method was the same, but the first has the merits of rapid sample preparation, reduced contamination risks and fast analysis.

Properties of low-modulus sodium silicate solution in alkali system

The properties of low-modulus(m≤1)sodium silicate and pre-desilication solutions in alkali systems were studied by measuring their electrical conductivity,viscosity,and surface tension.The results show that the property of high concentration pre-desilication solution is similar to that of sodium silicate solution.The electrical conductivity of sodium silicate solution increases with increasing the temperature and silica concentration but decreases with increasing the modulus.Further,the viscosity of the solution increases with increasing the silica concentration and linearly decreases with increasing the temperature,whereas its surface tension gradually decreases with increasing silica concentration and temperature,indicating that the sodium silicate solution is an oligomer with strong surface activity.At room temperature,the electrical conductivity and surface tension of sodium silicate solution are higher than those of pre-desilication solution,whereas its viscosity is smaller than that of pre-desilication solution.A turning point exists at a silica concentration of 44.7 g/L.When the silica concentration is less than 44.7 g/L,the ionic structure of the solution is dominated by monomeric silicate ions.In contrast,when the silica concentration changes from 44.7 to 50 g/L,the migration number of silicate anions significantly decreases.

The Use of Sodium Silicate as a Corrosion Inhibitor in a Saline Drilling Fluid: A Nonaggressive Option to the Environment

The function of a corrosion inhibitor in drilling mud compositions is the corrosion protection of the equipment involved in drilling operations. Many compositions involve environmentally several products such as fatty amines of high molecular weight, polyoxylated amines, amides, imidazolines, nitrogen heterocyclic products, etc. The potential advantages of the use of silicates are the effective protection of carbon steel, especially in aerated saline fluids, low costs and non-aggressive behavior to environment. Gravimetric and electrochemical tests were carried out using an aerated solution of 3.5% NaCl and the addition of sodium silicate (Na2SiO3·9H2O) as a corrosion inhibitor at concentrations of 250 to 2000 mg/L. The efficiencies of the corrosion protection of carbon steel using silicate concentrations greater than 1250 mg/L were greater than 92%.

A flexible CNT@nickel silicate composite film for high-performance sodium storage

Due to the sufficient ion diffusion channels provided by the large interlayer spacing, layered silicates are widely considered as potential anode materials for lithium ion and sodium ion batteries. However, due to the poor electronic conductivity, the application of layered silicates for electrochemical energy storage has been greatly limited. Carbon nanotube(CNT) film has excellent electrical conductivity and a unique interconnected network, making it an ideal matrix for composite electrochemical material. We herein report a CNT@nickel silicate composite film(CNT@NiSiO) fabricated by a SiO2-mediated hydrothermal conversion process, for sodium storage with excellent electrochemical properties. The obtained composite possesses a cladding structure with homogeneous nanosheets as the outermost and CNT film as the inner network matrix, providing abundant ion diffusion channels, high electronic conductivity, and good mechanical flexibility. Due to these merits, this material possesses an excellent electrochemical performance for sodium storage, including a high specific capacity up to 390 mAh g-1 at 50 mA g-1, good rate performance up to 205 mAh g-1 at 500 mA g-1, and excellent cycling stability. On this basis, this work would bring a promising material for various energy storage devices and other emerging applications.

Evaluation of the effect of sodium silicate addition to mine backfill,GelfillLPart 1

In this paper, the mechanical properties of sodium silicate-fortified backfill, called Gelfill, were investigated by conducting a series of laboratory experiments. Two configurations were tested, i.e. Gelfill and cemented hydraulic fill（CHF）. The Gelfill has an alkali activator such as sodium silicate in its materials in addition to primary materials of mine backfill which are tailings, water and binders. Large numbers of samples of Gelfill and CHF with various mixture designs were cast and cured for over 28 d. The mechanical properties of samples were investigated using uniaxial compression test, and the results were compared with those of reference samples made without sodium silicate. The test results indicated that the addition of an appropriate amount of an alkali activator such as sodium silicate can enhance the mechanical（uniaxial compressive strength） and physical（water retention） properties of backfill. The microstructure analysis conducted by mercury intrusion porosimetry（MIP） revealed that the addition of sodium silicate can modify the pore size distribution and total porosity of Gelfill, which can contribute to the better mechanical properties of Gelfill. It was also shown that the time and rate of drainage in the Gelfill specimens are less than those in CHF specimens made without sodium silicate. Finally, the study showed that the addition of sodium silicate can reduce the required setting time of mine backfill, which can contribute to increase mine production in accordance with the mine safety.

Effect of aggressive pH media on peat treated by cement and sodium silicate grout

The effects of aggressive peat nature (pH) on the strength of peat treated by cement and cement-sodium silicate grout were investigated by evaluating the changes in unconfined compressive strength,moisture content,and scanning electron microscopy (SEM) of samples with time in different pH media.The results indicate that peats treated by cement-silicate have higher strength than peats treated by cement,due to an increase in pH value of the media.Furthermore,cement and cement-silicate are highly effective in reducing the moisture content and void ratio of the treated peats.The microstructures of treated peats support the laboratory test results.