Silica Samples Research Articles

Effect of Laser Power and Diamond Tool Parameters for Micro Laser-Assisted Ductile Mode Material Removal on Fused Silica

Abstract Fused silica is an essential material used in various applications due to its excellent optical and mechanical properties. However, processing it can be challenging due to its high hardness and brittleness, leading to sub-surface damage during grinding and polishing operations. Micro laser-assisted ductile mode material removal is a promising technique for achieving high levels of precision and accuracy in material removal. This technique leads to controlled and precise removal of material without inducing cracks or fractures. Despite its advantages, there are several challenges associated with the process, such as selecting the appropriate laser power and diamond tool geometry. In this study, we employed a Universal Mechanical Tester equipped with modified OPTIMUS, a laser-assisted machining technology to investigate the impact of laser and diamond tool geometry on scratch cut quality. Introducing and increasing the laser power demonstrated an improvement of around 251.7% in cut ductility, leading to a decrease in the severity of sub-surface damage (SSD). Altering the rake angle from -25° to -45° resulted in a 45.3% reduction in the critical depth of cuts (DOCs). However, when laser was employed, the critical DOCs increased around 34.4% in ductile mode material removal on fused silica samples, which underscores the criticality of the laser in this process.

Preparation and characterization of fumed silica added PMMA denture base materials

This study was carried out to investigate the chemical, mechanical, and structural properties of increasing amounts of fumed silica added to PMMA denture base material. The effect of adding fumed silica at three different concentrations (0.5%, 1%, and 2% by weight) to PMMA was studied using Fourier transform infrared spectroscopy (FTIR), dynamic mechanical analysis (DMA), density, flexural strength, hardness, atomic force microscopy (AFM), and scanning electron microscopy (SEM). The results showed that the highest flexural strength values (105.64 MPa) and hardness (20.07 microvickers) were obtained with 1% wt. of fumed silica material. According to DMA results, fumed silica samples containing 1% wt. had the highest energy storage (3.24 GPa at 30 °C) and glass transition temperature. As a result, fumed silica in PMMA denture base material reached its maximum saturation limit at 1% wt. A more brittle behavior was observed in samples containing 2% fumed silica, which accumulated on the surface, as confirmed by AFM. The molecular bonds at the resin-fumed silica interface weaken due to the agglomeration of fumed silica. Consequently, the flexural strength and hardness decrease, along with the glass transition temperature and storage modulus. The potential applications of this research are vast, inspiring further exploration and innovation in denture-based materials.

Ultrafast T1-T1ρ NMR for Correlating Different Motional Regimes of Molecules.

Nuclear magnetic resonance (NMR) relaxation times provide detailed information about molecular motions and local chemical environments. Longitudinal T1 relaxation time is most often sensitive to relatively fast, nano- to picosecond ranges of molecular motion. Rotating frame T1ρ relaxation time reflects a much slower, micro- to millisecond range of motion, and the motional regime can be tuned by changing spin-lock field strength. Conventional methods for measuring T1 and T1ρ relaxation times are time-consuming, since experiments must be repeated many times with incremented magnetization recovery or decay delay. In this work, we introduce two novel and efficient NMR methods to correlate the T1 and T1ρ relaxation times. The first method, IR-SPICY, combines the conventional T1 inversion recovery (IR) with the single-scan T1ρ detection-based spin-lock cycle (SPICY). The second method, ultrafast (UF) IR-SPICY, allows measurement of whole two-dimensional T1-T1ρ correlation data in a single scan, in a couple of seconds, based on spatial encoding of the T1 dimension. We demonstrate the performance of the methods by studying relaxation of water in porous silica and hydrogel samples, latter acting as a model of the articular cartilage extracellular matrix. The methods allow correlating different molecular motional regimes, potentially providing unprecedented information about various chemical and biochemical systems, such as structures and fluid dynamics in porous materials, macromolecular changes in tissues, and protein dynamics. One to three orders of magnitude shortened experiment time enable the studies of changing or degrading samples. Furthermore, the single-scan approach may significantly facilitate the use of modern nuclear-spin hyperpolarization techniques to enhance the sensitivity of T1-T1ρ measurements by several orders of magnitude.

Investigation of the thermal conductivity of SiO2 glass using molecular dynamics simulations

AbstractA recent study showed that generating local crystalline paths within a glassy matrix provides only a moderate increase in thermal conductivity until the path fills most of the total volume. It was indicated that percolation theory governs the thermal conductivity in such crystalline‐implanted glass composites. In this study, we use computer simulations to investigate the effect of partial vitrification by breaking structural order of silica crystals by local vitrification. Such locally vitrified crystal structures are made by the bond‐transposition method, where the extent of vitrification can be tuned. Also, we test melt‐quenching of three SiO2 crystalline structures (α‐quartz, coesite, and stishovite) to make silica glasses with different densities. The cooling rates and pressures were varied during the melting process in order to obtain glass structures with varied degrees of order. Our results show that the thermal conductivity of silica glasses calculated using Green–Kubo relation decreases rapidly as soon as the crystallinity is disturbed by bond transition or generated local glassy phase. This implies the phonon mean free path rapidly shrinks with even a small number of scatterers, regardless of the original polymorph. Through the investigation of the pressure effect, a strong proportional relation between the thermal conductivity and the density is found among all silica samples. Such correlation can be accounted by assuming a constant integral term in the Green–Kubo relation without the volume scaling, which is reasonable based on a weak dependence of κV on the density of silica glass except with a slight increase at low quench pressures. We hypothesize that when the quench pressure increases moderately, an increase of characteristic ring size tends to generate a more flexible SiO2 structure which results more phonon scattering. Green–Kubo modal analysis further shows that the contribution from modes at low frequencies is suppressed when SiO2 is melt‐quenched at higher pressure and vice versa.

Impregnation of Silica Gel with Choline Chloride-MEA as an eco-friendly adsorbent for CO2 capture

Deep eutectic solvents (DES) are a generation of ionic liquids that benefit from low cost, good stability, and environmental-friendly features. In this research, a porous silica gel was impregnated with a eutectic Choline Chloride-Monoethanolamine solvent (ChCl-MEA) to greatly improve its CO2 capture performance. In the impregnation, the weight percentages of ChCl-MEA were used in the range of 10–60 wt% at a temperature of 25 °C. The effect of ChCl-MEA loading on the structural properties of the DES-modified silica samples was studied by BET, FTIR, and TGA analyses. Investigation of the CO2 adsorption performance at different operational conditions showed that the modified silica gel with 50 wt% ChCl-MEA (Silica-CM50) presents the highest CO2 capture capacity of 89.32 mg/g. In the kinetic modeling, the fractional order model with a correlation coefficient of 0.998 resulted in the best fit with the experimental data. In addition, the isotherm data for Silica-CM50 were well-fitted with the Dual site Langmuir isotherm model with a correlation coefficient of 0.999, representing two distinct sites for the adsorption process. Moreover, the thermodynamic parameters including Enthalpy, Entropy, and Gibbs free energy at 25 °C were obtained to be − 2.770, − 0.005 and − 1.162, respectively. The results showed the exothermic, spontaneous and feasibility of the adsorption process.

Highly stable mesoporous Ni-phyllosilicate particle under high temperature hydrothermal and base conditions towards industrial catalytic applications

Two mesoporous nickel phyllosilicate (Ni-PS) samples with Ni/Si ratios of 0.3 and 1 were used to compare high-temperature hydrothermal stability. The Ni-PS structures have well-developed porosity and pore size distributions mainly ranging from 2 to 20 nm. To assess their hydrothermal resistance as a reusable heterogeneous catalyst in high-temperature reactions, the samples were exposed to 800 °C for 7 days using steam-supplied muffle furnaces. Three types of mesoporous silica samples (i.e. MCM-41, SBA-15, and mesoporous benzene-silica) and two zeolites (i.e. ZSM-5 and zeolite-Y) were compared under the same conditions. The hydrothermal resistance was primarily confirmed based on changes in pore size distribution and surface area through nitrogen-sorption isotherm analysis. The crystal structure and the binding energy of each sample were investigated by X-ray diffraction and X-ray photoelectron spectroscopy measurements. The Ni-PS structures displayed excellent stability (i.e. BET surface area retained over 77 % and 65 % after 1-d and 7-d treatment, respectively.) compared with other mesoporous samples, and even higher stability than zeolite Y. In addition, structural stability at pH = 10 is much higher than that of ZSM-5. This suggests that it could be used for various catalytic chemical reactions including hydrogenation and cracking processes because NiO and Ni nanoparticles are uniformly distributed on the surface, maintaining their particle shape even after a reduction process.

Measure for optical robustness of directly bonded glass-to-glass joint using its interaction with damage induced by fs laser.

To produce more powerful compact ultrafast lasers, research aims at improving the quality of bonds between components inside the laser cavity. Increasing bond robustness under optical irradiation helps the bonds to survive the high energy pulses that these lasers are designed to produce. A measure for such robustness is reported here to support work toward improved bonding processes for such lasers. We produced bonds between pairs of optical grade fused silica glass cylinders using a wet direct bonding procedure. We evaluated these bonds using conventional microscopy, including scanning electron microscopy (SEM) and optical microscopy, without quantifiable results. The bond interface was not discernible through conventional SEM imaging, even after cross sectioning and polishing. The majority of the interface was also undetectable in optical micrographs, except for some limited areas of interfacial disturbance. To obtain quantifiable results for optical robustness, we used an 800nm femtosecond laser to produce filament-shaped damage from a focal spot moving across the interface. Microscopy of the damage showed its interaction with the interface, the presence of which caused a ≈0.130 to ≈0.230mm long interruption in the damage line. The exact value depended not only on laser power but also interface quality, and thereby quantified the optical robustness. The reported method proved more sensitive in detecting bonds of fused silica samples compared to other visualization techniques used. Our results suggest a nuanced understanding of bonded glass joints-mechanically sound, yet with limited optical robustness under specific laser conditions.

One-step functionalization and polymer grafting potential of green silica derived from rice husk ash

Green silica has been synthesized from rice husk ash which exempts the landfilling of agricultural waste and the requirement of higher temperature for digestion, unlike the conventional mode of silica synthesis making the process of precipitation and functionalization sustainable. An energy-efficient method of functionalization has been optimized for the synthesis of functionalized silica from rice husk ash via co-condensation. The potential for providing better reinforcement leads silica to be used as filler in composite manufacturing. To obtain a better silica-polymer interaction, nitroxide functionalized silica has been synthesized over three different types of silica samples using different processes. The nitroxide functionalities were introduced by thiol-ene reaction between 4-acryloyloxy(2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO) and mercaptopropyl functionalized silica particles. The mercaptopropyl functionalized silica was synthesized by post-modification as well as co-condensation over commercial precipitated silica, commercial rice husk ash silica, and silica synthesized in the lab from sodium silicate obtained from rice husk ash. By comparing mercaptopropyl and nitroxide grafting density, it has been observed that the nitroxide loading highly depends on the method of functionalization and the co-condensed samples show higher nitroxide loading compared to the post-modified samples. The nitroxide functionalized samples were further subjected to polystyrene grafting, and the efficiency of surface nitroxide radicals in capturing the polymer radicals with respect to nitroxide loading was determined. The grafting density was observed to increase with the increase in conversion and the increase in the initiator-to-monomer ratio. However, the grafting density was observed to be saturated at some point despite having a higher surface area and surface nitroxide radicals. The study can be used to tune the surface nitroxide radical concentration and surface area for optimum polymer grafting for engineering applications.

Experimental Study on Evolution of Chemical Structure Defects and Secondary Contaminative Deposition during HF-Based Etching

Post-processing based on HF etching has become a highly preferred technique in the fabrication of fused silica optical elements in various high-power laser systems. Previous studies have thoroughly examined and confirmed the elimination of fragments and contamination. However, limited attention has been paid to nano-sized chemical structural defects and secondary precursors that arise during the etching process. Therefore, in this paper, a set of fused silica samples are prepared and undergo the etching process under different parameters. Subsequently, an atomic force microscope, scanning electron microscope and fluorescence spectrometer are applied to analyze sample surfaces, and then an LIDT test based on the R-on-1 method is applied. The findings revealed that appropriate etching configurations will lead to certain LIDT improvement (from initial 7.22 J/cm2 to 10.76 J/cm2), and HF-based etching effectively suppresses chemical structural defects, while additional processes are recommended for the elimination of micron- to nano-sized secondary deposition contamination.

Adsorption of Diffusing Tracers, Apparent Tortuosity, and Application to Mesoporous Silica.

The apparent tortuosity due to adsorption of diffusing tracers in a porous material is determined by a scaling approach and is used to analyze recent data on LiCl and alkane diffusion in mesoporous silica. The slope of the adsorption isotherm at small loadings is written as β = qA/qG, where qA is the adsorption-desorption ratio and qG = ϵ/(as) - 1 is a geometrical factor depending on the range a of the tracer-wall interaction, the porosity ϵ, and the specific surface area s. The adsorption leads to a decrease of effective diffusion coefficient, which is quantified by multiplying the geometrical tortuosity factor τgeom by an apparent tortuosity factor τapp. In wide pores or when the adsorption barrier is high, τapp = β + 1, as obtained in previous works, but in narrow pores there is an additional contribution from frequent adsorption-desorption transitions. These results are obtained in media with parallel pores of constant cross sections, where the ratio between the effective pore width ϵ/s and the actual width is ≈0.25. Applications to mesoporous silica samples are justified by the small deviations from this ideal ratio. In the analysis of alkane self-diffusion data, the fractions of adsorbed molecules predicted in a recent theoretical work are used to estimate τgeom of the silica samples, which is ≫1 only in the sample with the narrowest pores (nominal 3 nm). The application of the model to Li+ ion diffusion leads to similar values of τgeom and to a difference of energy barriers of desorption and adsorption for those ions of ∼0.06 eV. Comparatively, alkane self-diffusion provides the correct order of magnitude of τgeom, with adsorption playing a less important role, whereas adsorption effects on Li+ diffusion are much more important.

Geochemistry and mineralogy of modern floodplain Nile sediments of Sohag area, Egypt: an environmental perspective

Understanding the characteristics of modern floodplain sediment (MFS) is important for geomorphological, paleoclimatic, sedimentation, and environmental investigations. We collected samples from present floodplain Nile sediments in Egypt’s Sohag area and used mineralogical and geochemical (i.e., major and trace elements) proxies to investigate the characteristics and establish their provenances, climatic conditions during deposition, and weathering influence. The study revealed that the Nile floodplain sediments are composed mainly of silt (26–77%), clay fraction (7–44%), and sand content (3–63%), and their texture is classified as clayey silt. These sediments are classified geochemically as greywacke to shale. The mineralogical studies revealed two main assemblages of heavy minerals: the first assemblage represented by magnetite, goethite, zircon, epidote, and garnet and reflects the basement complex in the Eastern Desert and its surrounding rocks; and the second assemblage of goethite, pyroxene, hornblend, and mica of fooldplain deposits derived from the Ethiopian highlands. The geochemical studies indicate that the Nile sediments are immature and formed due to the moderate degree and nonsteady chemical weathering of the parent rocks. The geochemical studies show different mixed sources of sediments, where fine sediments are mostly mafic igneous with a partial contribution from siliscic sedimentary rocks, while the coarser ones are derived mainly from siliscic sedimentary and acidic igneous rocks. The sediments of the presented modern fooldplain reflected two different tectonic setting source areas (collision and continental rift tectonic setting for high silica and low silica samples, respectively) that were shared in supplying the sediments to the present basin. The study revealed that the investigated area may become desertified as a result of climate change and human activities such as salinity, fertiliser use, sand encroachment, and pollution.

Accurate Determination of the Low-Light-Level Absorption of DUV-Fused Silica at 193 nm with Laser Calorimetry

The low-light-level absorption coefficient of OH-contained and H2-impregnated synthetic fused silica material in 193 nm optical lithography application is determined via a laser calorimetry measurement. The fluence and repetition rate dependences of the absorptances of the deep ultraviolet (DUV)-fused silica samples with different thickness are measured. The measured dependences are fitted to a theoretical model, taking into consideration the generation and annealing of laser irradiation induced defects. The surface absorption, the low-light-level linear absorption coefficient, as well as the nonlinear absorption coefficient of the fused silica material are accurately determined via the fitting. The low-light-level linear absorption coefficients determined via the fluence dependence and the repetition rate dependence are in good agreement, demonstrating the reliability of the measured low-light-level absorption coefficient, which is the key parameter to the determination of the internal transmission of the DUV-fused silica material used in the 193 nm optical lithography.

Pivotal role of pH value in the preparation of mesoporous silica with high surface area for toluene adsorption

Porous silica samples were prepared by a non-template approach using silicate and HCl at different pH values. Macroporous silica with a low surface area of 72.0 m2/g was obtained at pH = 7. Surprisingly, mesoporous silica with very high surface area of 806.0 m2/g was obtained at pH = 3. This was due to the formation of protonated silicic acid molecules under acidic condition which had enough time for the polymerization and assembly to mesoporous structure, and the rapid polymerization and assembly of silicic molecules under neutral condition to silica nanoparticles among which macropores were formed. The mesoporous silica showed a saturation toluene adsorption capacity of 79.1 mg g−1, 9 times higher than that of the macroporous silica.

Controllable Synthesis of Hollow Silica Nanospheres

Nano hollow SiO2 refers to a unique form of nanoscale silica material that has an inner cavity structure. This hollow configuration offers several advantages over solid structures, including a larger specific surface area, lower density, and improved permeability. Additionally, hollow silica is chemically inert and thermally stable, making it an excellent candidate for drug delivery applications. Silica's transparency to both light and magnetism ensures that it does not absorb light or disrupt magnetic fields, preserving the inherent optical or magnetic properties of certain composites. In addition, its porosity, biocompatibility, and mechanical stability are adjustable and controllable, making it an ideal and cost-effective material for both industrial and biological uses. This study synthesised a range of hollow spherical silica samples via the sol-gel process. The aim was to investigate the impact of different factors on their sphericity and wall thickness.

Silica exposure among miners at high altitude. Inhaled dose and evaluation methods in hypobaric environments

To evaluate silica exposure among Chilean miners at high altitude, using different methodological approaches, for the purpose of determining the safest method to control exposures. Methods: The 46 miners in the sample worked at 3000 meters above sea level in nonstandard work shifts, consisting of four consecutive 12-hour days, followed by four consecutive days off. Silica samples were obtained in each of the jobs positions of these 46 high-altitude miners. The results of the concentrations are presented in mg/m3. Exposures were evaluated in compatison to the Threshold Limit Value (Method 1) and using two other methodologies that incorporate respiratory parameters (Methods 2 and 3). The proportion of miners at risk was determined with each of these methods and compared. Based on the Threshold Limit Value (Method 1), 43.48% of miners were classified as being at risk. With the other two methods that incorporate respiratory parameters, the proportion of overexposed miners was 82.61% with Method 2, and 73.91% with Method 3. Of the three methods analyzed, the one that considers the respiratory parameter minute volume, through the estimation of the inhaled dose, is the safest to define the group of miners at risk due to exposure to silica at high altitude.

A novel atomic removal model for chemical mechanical polishing using developed mesoporous shell/core abrasives based on molecular dynamics.

To improve polishing performance and reduce the environmental pollution of chemical mechanical polishing (CMP) tests, mesoporous shell/core silica abrasives were prepared, and a novel green CMP slurry was developed, including sorbitol, hydrogen peroxide and sodium carbonate. Prior to CMP, fused silica was roughly polished with ceria slurry. Using developed mesoporous abrasives, surface roughness Sa is reduced from 0.347 to 0.253 nm for a scanning area of 200 × 200 μm2, and the material removal rate (MRR) is increased from 70 to 127 nm min-1, compared with traditional solid abrasives. Based on molecular dynamics (MD) simulations, a novel atomic removal model is proposed for mesoporous abrasives through the immediate elastic recovery of atoms. MD simulations suggest that the formation of convex peaks and pits was inhibited by the mesoporous structure, promoting uniform distribution of surface atoms and atomic removal. This is different from a conventional simple increase of polishing times. In addition, more bridge bonds of Si-O-Si and a lower average Si-O bond order are produced in fused silica samples due to their mesoporous structure, contributing to a higher MRR.

Synthesis of SBA-16 mesoporous silica from rice husk ash for removal of Rhodamine B cationic dye: Effect of hydrothermal treatment time

Recently, the use of silica-containing wastes has gained popularity as an excellent pathway to prepare mesoporous silica materials for applications of adsorption, catalysis and energy. Hence, this report aimed to prepare SBA-16 mesoporous silica samples derived from rice husk ash under varying times during hydrothermal treatment (viz., 24 and 48 h) and named as SBA-16–24 h and SBA-16–48 h. FE-SEM, TEM, XRD, FTIR, Raman and N2 gas adsorption at − 196°C tools were performed to explore the formation of SBA-16. Rhodamine B (RhB) dye uptake from aqueous solutions by both samples was determined by equilibrium isotherms and kinetics. Effects such as pH, dye initial concentration, temperature and contact time were investigated. Results revealed the successful preparation of SBA-16 with an amorphous, ordered mesoporous structure and a higher total surface area of 461 m2/g for SBA-16–48 h obtained during a longer time of hydrothermal treatment. Increasing the time of hydrothermal treatment to 48 h decreased the average particle sizes of SBA from 50–40 nm to 20–10 nm with enhancing the total surface area, mesopore volume and amount of Si-O-Si groups. Equilibrium adsorption isotherms were fitted better by the Langmuir model than the Freundlich Temkin and Dubinin-Radushkevich models. The maximum adsorption capacity calculated from Langmuir model showed that SBA-16–48 h featuring the larger capacity of about 166.7 mg/g at pH 6. Pseudo-second order kinetic is found to be more suitable to describe the adsorption. Negative values of ΔH0 and ΔS0 thermodynamic parameters affirmed that the adsorption of RhB dye is an exothermic and spontaneous process over prepared mesoporous silica. Conclusively, the investigated SBA-16–48 h is a promising adsorbent for effective removal of basic dyes from their aqueous stream.

Adjusting the Si/Al ratio of high silica zeolites for efficient ethane and ethylene separation

The economically efficient separation of ethane (C2H6)/ethylene (C2H4) presents challenges in the petrochemical industry, and the use of traditional adsorbents zeolite provides a reliable guarantee for maintaining the economic viability of adsorption separation technology. In this study, we investigate the impact of different silica-alumina ratios (SiO2/Al2O3 = 40, 500, and 1500) of high silica zeolites ZSM-11 on the C2H6/C2H4 separation performance to develop efficient C2H6 selective adsorbents. The results show that the C2H6 adsorption capacity and C2H6/C2H4 selectivity of ZSM-11 increase as the silica-alumina ratios increases. The pure silica zeolite (ZSM-11(1500)) exhibits the highest adsorption capacity for C2H6 (59.19 cm3/g) and the highest selectivity for C2H6/C2H4 (2.04), which were superior to ultra-high silica sample (ZSM-11(500)) (55.06 cm3/g and 1.62, respectively) and high silica sample (ZSM-11(40)) (47.28 cm3/g and 1.23, respectively), at 273 K and 1 bar. The mixed gas breakthrough experiments results show that pure silica sample has outstanding C2H6/C2H4 separation ability. The PSA simulation calculated data demonstrating promising potential for industrial applications. Importantly, this separation performance remains unaffected even in the presence of H2O.

Density Functional Study of Structural and Vibrational Properties of α-Moganite

α-moganite is a recently discovered polymorph of silica, commonly intergrown with quartz in natural microcrystalline silica samples. An important challenge is finding an effective method for estimating its amount in a sample under study, which is important for its applications, related to the technology of growth of dielectric layers, as well as for fundamental problems, related to the formation of both terrestrial and lunar mineral deposits and biogenic formation. One of these methods is vibrational spectroscopy, with the help of which the presence of a particular compound is determined by the presence of characteristic spectral lines. In this work, the search for such lines is carried out using density functional theory calculations and comparisons of the IR and Raman spectra of α-quartz and α-moganite. With the help of such calculations, the stability of the moganite structure has been proven for the first time, and its spectral characteristics have been determined over the entire range of vibrational frequencies. Several new spectral lines characteristic of α-moganite were discovered in the 65–85 cm−1 region. Moreover, the evolution of spectral peculiarities under hydrostatic pressure was studied.

Silica extraction from bamboo leaves using alkaline extraction method

The silica is most common constituent of bamboo leaves mainly varies from 75.90 to 82.86 %.In this study, silica was extracted from bamboo leaves using an alkaline extractionprocess. In proximate analysis, bamboo leaves were found to contain significantly more ash (24.5 %) containing 79.28 % silica and low levels of fixed carbon. However, in ultimate analysis, bamboo leaves were found to contain 57.56 % oxygen.The yield and quality of silica were improved by extracting silica from bamboo leaves ash under various operating conditions.A higher concentration of NaOH (2.5 N) resulted in a greater yield of silica (97.73 %).During the alkaline process, an acid leaching treatment was used toremove metal impurities either from bamboo leaves ash or extracted silica. The silica yield increased from 97.73 % to 98.86 % after acid leaching of feed. In an FTIR analysis, Si-O-Si, Si-O, and Si-OH bonds were identified. Modern characterization techniques such as XRF were used to determine the purity of silica. There is a significant difference between the maximum purity of acid leached silica samples (96.13 %) and that of commercial silica samples (95.52 %).As a result of this study, silica that has a wide range of applications in the food and nutrition industries, the pharmaceutical industry, and as a nano-catalyst could be produced.