Porous Ceramic Substrate Research Articles

A novel TFNi pervaporation membrane with g-C3N4 quantum dots for high-efficiency IPA dehydration

Pervaporation (PV) shows significant potential for the highly selective isopropanol (IPA). The pursuit of developing PV membranes with outstanding separation effect and enduring high purity permeation is an indispensable goal. Based on polyamide (PA) separation layers, a polydopamine (PDA) mixed g-C3N4 quantum dots (gCNQDs) coating as the interlayer was deposited onto a porous ceramic hollow fiber substrate to fabricate thin-film nanocomposite membranes with an interlayer (TFNi). The nanocomposite interlayer enabled the formation of a smoother and highly separated selective polyamide layer. The separation factor exhibited a 31-fold enhancement with the augmentation of the blending fraction of gCNQDs during the PDA coating process. The resulting TFNi membrane attained an exceedingly high separation factor of 10270 ± 90 with a permeate water concentration of 99.9% and demonstrated a satisfactory flux of 1.40 ± 0.08 kg⋅m-2⋅h-1 during the PV process of 90 wt% IPA dehydration at 60 °C. This study presents a fresh perspective on the implementation of nanocomposite interlayers, which is expected to expand the application of high-performance TFNi membranes in PV dehydration processes.

Multiple layers, porous surface, and their role in increasing the efficiency of photocatalytic coating on (DD3, DD3+ZrO2) ceramics and glass

Magnesium-doped zinc oxide thin films were dip-coated onto porous ceramic and glass substrates under identical conditions (50 layers, same doping ratio). Structural, morphological, and photocatalytic properties were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), UV–visible spectrophotometry, and confocal microscopy. XRD analysis indicated a shift in peak positions towards higher angles, increased grain size, and lattice distortion on both substrates. Unique flower-shaped crystalline granulates were observed exclusively on the ceramic substrate (DD3Z). The energy gap decreased on the ceramic and increased on the glass substrate. The photocatalytic activity was evaluated using an aqueous orange II solution, showing significantly higher decomposition (80 ± 0.53 % after 6 h) on the ceramic compared to the glass substrate (30 %). The enhanced performance on ceramic substrates, particularly with DD3+ZrO2, was attributed to increased microporosity, surface roughness, and active material incorporation, facilitating greater photocatalytic efficiency. The findings suggest promising applications of these materials for efficient and cost-effective photocatalysis, with potential for reuse after thermal treatment at 500 °C.

Hydrogen permselective membrane prepared by plasma treatment of porous ceramic substrates

Abstract Demand for hydrogen is increasing as we move toward a decarbonized society. Membrane separation methods have attracted attention as a way to reduce the cost of hydrogen production. In this study, we focused on boron nitride (BN) as a chemically stable porous substrate material. CVD treatment at 250°C has been investigated for porous BN, but selectivity did not develop. Therefore, we focused on atmospheric pressure plasma as a treatment method. The objective of this study is to develop a membrane with high hydrogen selective permeance by immersion in silicon alkoxide after plasma treatment. After plasma treatment for 100 s, the H2 permeance was 3.52×10−6 [mol m−2 s−1 Pa−1] and the H2/N2 permeance ratio was 18.25. Since molecular hydrogen can pass between the BN crystal faces, it is considered that silica reacted with the hydroxy groups formed on BN by plasma treatment and blocked the space between crystals. Therefore, it is suggested that the performance of the separation membrane changes depending on the number and distribution of hydroxyl groups by plasma treatment, and further stabilization is needed.

Porous Ceramic Substrates for the Study of Biological Objects by Electron Microscopy

Porous Ceramic Substrates for the Study of Biological Objects by Electron Microscopy

Effect of Temperature on Porous Ceramic Substrates Supported ZnO Thin Films for Enhanced Photocatalytic Activity

In this study, eco-friendly and low-cost highly porous ceramic substrates were fabricated to enhance the performance of photocatalysts. ZnO as a model photocatalyst deposited as thin films by dip-coating sol-gel method on naturally extracted kaolin clay (90%) and Corn starch (10%)-made highly porous ceramic substrates prepared as pellet form and sintered at different temperatures: 1150, 1200, 1250, and 1300 °C. The effect of temperature on the prepared substrates modified their porosity and the best value obtained was 56% with a specific surface area of 38.80 m2/g for 1150 °C. Structural analysis of the X-ray diffraction spectra revealed a hexagonal wurtzite structure for ZnO and mullite/cristoballite structures for substrates. Scanning electron microscopy images confirmed the porosity and uniform formation of ZnO on the substrates. The high porosity samples resulted in a high reflectance of over 90%, and band gap energies values around 3.11 eV were verified by UV–VIS spectroscopy. The photocatalytic properties of ZnO thin films on ceramic substrates were studied by testing the degradation of Orange II dye in an aqueous medium under UV light irradiation. The highest degradation rate of 92% was obtained for ZnO thin films deposited on porous substrates treated at 1150 °C. The kinetic study indicated that the photocatalytic degradation of Orange II correlated with the pseudo-first-order kinetic model.

Photocatalytic properties of ZnO nanoparticle coating on porous ceramic substrates with varying porosities produced from fly ash and red mud

AbstractIn order to improve filtering efficacy, nanoparticles are often deposited as photocatalytic degrading agents onto porous ceramics. This study aimed to deposit ZnO nanoparticles on ceramic substrates produced from fly ash and red mud with adjustable porosity and investigate their photocatalytic properties. To achieve this goal, at first porous ceramics were produced and sintered at various temperature/time intervals. It was observed that sintering at 800°C for 120 min provided a proper structure and porosity. In addition, MgO replacement with MgCO3 lowered the water absorption of the samples from 25.63% to 11.45%. The samples were then coated with ZnO nanoparticles using the sol–gel method and the ZnO structures obtained were micron‐sized plates. It was observed that increasing porosity increased the ZnO amount and accordingly the photocatalytic properties of the products. During the adsorption tests conducted in the dark, the coated ceramic samples were stained with MB with a maximum MB adsorption ratio of ∼14%. On the other hand, no visible MB stain was observed on the samples that were exposed to UV irradiation, and the MB removal after the UV irradiation was 93.6%; therefore, it was concluded that the dominant MB removal mechanism was photocatalytic.

Leaf yield and mineral content of mizuna in response to cut-and-come-again harvest, substrate particle size, and fertilizer formulation in a simulated spaceflight environment

The Veggie plant-growth unit deployed onboard the International Space Station (ISS) grows leafy vegetables to supplement crew diets. “Cut-and-come-again” harvests are tested to maximize vegetative yield while minimizing crew time. Water, oxygen, and fertilizer delivery to roots of leafy greens growing in microgravity have become the center of attention for Veggie. Current Veggie technology wicks water into particulate root substrates incorporating controlled-release fertilizer (CRF). Mizuna mustard (Brassica rapa) was grown under ISS-like environments in ground-based Veggie-analogue units comparing crop response to combinations of two different substrate particle sizes, two different fertilizer formulations, and three leaf-harvest times from each plant. Fine-particle porous ceramic substrate (Profile©) was compared with a 40:60 mix of fine-particle porous ceramic Profile© + coarse porous ceramic Turface© substrate. Identical 18-6-8 (NPK) CRF formulations consisting of [50% fast-release (T70) + 50% intermediate-release (T100) prills] vs. [50% fast-release (T70) + 50% slow-release (T180) prills] were incorporated into each substrate, and leaf tissues were harvested from each treatment combination at 28, 48, and 56 days after sowing. The combination of T100 CRF in 100% Profile© substrate gave the highest fresh mass (FM) and leaf area (LA) across harvests, whereas T180 CRF in 40% Profile© gave the lowest. Dry-mass (DM) yields varied with effects on leaf area. Tissue nitrogen (N) and potassium (K) specific contents declined across harvests for all treatment combinations but tended to be highest for T100 CRF/100% Profile©, and lowest for T180 CRF/40% Profile©. These major macronutrients were taken up faster by roots growing in small particle-size substrate incorporating intermediate-rate CRF, but also were depleted faster from the same treatment combination, suggesting it may not continue to be the best combination for additional harvests. Micronutrients did not decline in tissue specific content across treatment combinations, but manganese (Mn) accumulated in leaf tissue across treatments and apparently comes mainly from the ceramic substrate, regardless of particle size. Substrate leachate analysis following final harvest indicated that pH remained in the range for nominal availability of mineral nutrients for root uptake, but electro-conductivity measurements suggested depletion of fertilizer salts from root zones, especially from the treatment combination supporting the highest yields and major macronutrient contents. Although 100% Profile© was the better growth substrate for mizuna in combination with intermediate-rate CRF and three cut-and-come-again harvests in ground-based studies, mixed-particle-size substrates may be a better choice for plant growth under microgravity conditions, where capillary forces predominant and tend to cause saturation of a fine medium with water. Since there were no statistically significant interactions between substrate and fertilizer in this study, our ground-based findings for CRF choice should translate to the best substrate choice for microgravity, but if NASA wants to consider additional cut-and-come-again harvests from the same mizuna plants, more complex CRF formulations likely will have to be investigated.

Deoxygenation of CO<sub>2</sub> Solvent Based on Monoethanolamine in Gas–Liquid Membrane Contactors Using Composite Membranes

This work is devoted to the removal of dissolved oxygen from a model solvent based on monoethanolamine (MEA) to prevent its oxidative degradation during the absorption purification of flue gases from carbon dioxide. Composite membranes based on porous ceramic and polymer substrates with a thin selective layer of poly[1-(trimethylsilyl)-1-propyne] and its mixture with polyvinyltrimethylsilane have been developed. Gas-liquid membrane contactors have been created on their basis. It is shown that with their use in the vacuum mode, up to 60% of dissolved oxygen can be removed from the model solvent.

From superhydrophilicity to superhydrophobicity: high-resolution neutron imaging and modeling of water imbibition through porous surfaces treated with engineered nano-coatings

This paper reports on a superhydrophilic to superhydrophobic transformation of TiO2 nanoparticles doped zinc phosphate coating systems when a hydrophobic agent is applied. The objective of the reported research was to demonstrate the feasibility of a neutron imaging technique for evaluating the performance of the proposed nano-coating system and reveal the differences in water ingress mechanisms which are specific to plain, superhydrophilic, overhydrophobic, and superhydrophobic specimens. The engineered nano-coatings were designed to improve hydrophobic response with inducing the required roughness pattern and introducing the photocatalytic performance. The effectiveness of the coatings was assessed using high-resolution neutron imaging (HR-NI), SEM, CLSM, and XRD techniques. High-resolution neutron imaging revealed that the superhydrophobic coating effectively prevents water ingress into the porous ceramic substrate, whereas water imbibition was observed for superhydrophilic coating during the test duration. The moisture transport kinetics was modeled based on the Richards equation for plain ceramic and superhydrophilic specimens using obtained penetration depth values from HR-NI. SEM, CLSM, and XRD studies confirm the desired TiO2-doped zinc phosphate coatings with increased surface roughness, photocatalytic reactivity, and chemical bonding. The research results demonstrated that a two-layer superhydrophobic system is capable of creating effective water barriers on the surface with contact angles of 153°, which remained effective even after surface damage.

A Combined Gas and Water Permeances Method for Revealing the Deposition Morphology of GO Grafting on Ceramic Membranes.

The adhesion enhancement of a graphene oxide (GO) layer on porous ceramic substrates is a crucial step towards developing a high-performance membrane for many applications. In this work, we have achieved the chemical anchoring of GO layers on custom-made macroporous disks, fabricated in the lab by pressing α-Al2O3 powder. To this end, three different linkers, polydopamine (PDA), 3-Glycidoxypropyltrimethoxysilane (GPTMS) and (3-Aminopropyl) triethoxysilane (APTMS), were elaborated for their capacity to tightly bind the GO laminate on the ceramic membrane surface. The same procedure was replicated on cylindrical porous commercial ZrO2 substrates because of their potentiality for applications on a large scale. The gas permeance properties of the membranes were studied using helium at 25 °C as a probe molecule and further scrutinized in conjunction with water permeance results. Measurements with helium at 25 °C were chosen to avoid gas adsorption and surface diffusion mechanisms. This approach allowed us to draw conclusions on the deposition morphology of the GO sheets on the ceramic support, the mode of chemical bonding with the linker and the stability of the deposited GO laminate. Specifically, considering that He permeance is mostly affected by the pore structural characteristics, an estimation was initially made of the relative change in the pore size of the developed membranes compared to the bare substrate. This was achieved by interpreting the results via the Knudsen equation, which describes the gas permeance as being analogous to the third power of the pore radius. Subsequently, the calculated relative change in the pore size was inserted into the Hagen-Poiseuille equation to predict the respective water permeance ratio of the GO membranes to the bare substrate. The reason that the experimental water permeance values may deviate from the predicted ones is related to the different surface chemistry, i.e., the hydrophilicity or hydrophobicity that the composite membranes acquire after the chemical modification. Various characterization techniques were applied to study the morphological and physicochemical properties of the materials, like FESEM, XRD, DLS and Contact Angle.

Fabrication of highly active and stable Ni/CeO2-nanorods wash-coated on ceramic NZP structured catalysts for scaled-up CO2 methanation

The production of synthetic natural gas from CO2 methanation using green H2 produced via water electrolysis is a promising pathway regarding both the curtailment of excess power by variable renewables and the mitigation of CO2 emissions. Several catalytic systems have been employed for thermocatalytic CO2 methanation in lab-scale, with Ni-based catalysts being amongst the most cost-effective and active materials. In this regard, we have recently demonstrated the remarkable low-temperature CO2 methanation activity of a nickel catalyst supported on ceria nanorods, ascribed to the augmented metal-support synergy. Herein, we report on a scaled-up process of CO2 methanation, involving; i) fabrication of a highly porous NZP-type ceramic substrate of Ba1+xZr4P6–2xSi2xO24 in the form of extruded pellets, ii) wash-coating of Ni/CeO2-nanorods catalyst on NZP pellets, iii) design and testing of scaled-up experiments under a scaling factor of 80:1 and 65:1 in terms of mass and volume of catalysts compared to lab-scale experiments, respectively. The as-synthesized catalyst exhibited remarkable performance under variable reaction conditions and stable behavior after 75 h. Remarkably, the structured catalyst attained a methane formation rate of 277 NL gNi−1 h−1, being higher to numerous values reported in relevant works. Equally importantly, it was disclosed that increased values of space velocity led to high temperature gradient in the catalytic bed, thereby favoring the generation of CO. Intriguingly, the morphological and structural characteristics of the used catalyst remained unaltered even after various on/off reaction cycles and the stability test, which is a promising finding toward scaling-up the process at higher technology readiness levels using real feed streams.

Polyamide nanofiltration membrane with MoS2 interlayer on tubular ceramic substrate for desalination

The tubular ceramic substrate has great potential in membrane separation because of its excellent solvent and temperature resistance, pressure stability, and long service life. However, it is still a challenge to prepare an ultrathin intact selective layer by interfacial polymerization (IP) on a porous tubular ceramic substrate, due to its large pore size and defects on the surface. In this study, a molybdenum sulfide (MoS2) interlayer with a loose structure was formed on the tubular ceramic substrate via hydrothermal, which provided a large surface area and fast transport channels. Subsequently, a polyamide (PA) skin layer was formed on the MoS2 interlayer through the IP procedure to obtain a composite membrane for desalination. The prepared PA/MoS2/ceramic composite membrane showed excellent water permeance of 17.7 L·m−2·h−1·bar−1 with a 96.8 % rejection of Na2SO4. Moreover, the prepared membranes showed good pressure resistance and long-term stability under cross-flow filtration within 30 days.

Development of evaporation technique for concentrating lead acid wastewater from the battery recycling plant, by nanocomposite ceramic substrates and solar/wind energy

Wastewater from car battery recycling plants contains lead ions. This acidic wastewater was treated by the solar steam generation method. In this research, a light porous ceramic substrate (PCS) was made based on clay, human hair, and nano-hydroxyapatite. The physical and chemical characteristics of this PCS were identified by SEM, XRD, FTIR, BET, and TGA. The high porosity in PCSs was created due to the removal of human hair in the calcination process inside the furnace. Microchannels with capillarity and hydrophilicity of nano-hydroxyapatite quickly pump water molecules to the surface of PCSs. The wastewater treatment process was carried out on two laboratory and semi-industrial scales. The temperature of the surface of the PCSs reached 70 °C in less than 60 min with the radiant heat transfer mechanism, and the water molecules were evaporated with an evaporation rate and thermal conversion efficiency were 9.22 Kgm−2h−2 and 90%, respectively. The wind blew the vapor away from the system and the rate of evaporation increased. PCSs had the ability to regenerate after several consecutive cycles.

Composite GO/Ceramic Membranes Prepared via Chemical Attachment: Characterisation and Gas Permeance Properties.

Graphene oxide (GO) oligo-layered laminates were self-assembled on porous ceramic substrates via their simple dip-coating into aqueous GO dispersions. To augment the stability of the developed composite GO/ceramic membranes and control the morphology and stacking quality of the formed laminate, short-((3-glycidoxypropyl)trimethoxy silane-GLYMO, (3-aminopropyl)triethoxy silane-APTES), and long-chain (polydopamine-PDA) molecules were involved and examined as interfacial linkers. A comparative study was performed regarding the linker's capacity to enhance the interfacial adhesion between the ceramic surface and the GO deposit and affect the orientation and assemblage characteristics of the adjacent GO nanosheets that composed the formed oligo-layered laminates. Subsequently, by post-filtrating a GO/H2O suspension through the oligo-layered laminate membranes, the respective multi-layered ones have been developed, whereas ethylenediamine (EDA) was used in the suspension as an efficient molecular linker that strongly bonds and interlocks the GO nanosheets. The definition of the best linker and approach was conducted on macroporous α-alumina disks, due to the use of inexpensive raw materials and the ability to fabricate them in the lab with high reproducibility. To validate the concept at a larger scale, while investigating the effect of the porous substrate as regards its micrometer-scale roughness and surface chemistry, specific chemical modifications that yielded membranes with the best gas permeability/selectivity performance were replicated on a commercial single-channel monolith with a ZrO2 microfiltration layer. XRD, Raman, ATR, FESEM, and XPS analyses were conducted to study the structural, physicochemical, surface, and morphological properties of the GO/ceramic composite membranes, whereas permeance results of several gases at various temperatures and trans-membrane pressures were interpreted to shed light on the pore structural features. Concerning the short-chain linkers, the obtained results ascertain that GLYMO causes denser and more uniform assembly of GO nanosheets within the oligo-layered laminate. PDA had the same beneficial effect, as it is a macromolecule. Overall, this study shows that the development of gas-separating membranes, by just dipping the linker-modified substrate into the GO suspension, is not straightforward. The application of post-filtration contributed significantly to this target and the quality of the superficially deposited, thick GO laminate depended on this of the chemically attached oligo-layered one.

Melded ceramic membranes: A novel fabrication method for ultrathin alumina membranes of high performance

AbstractConventional ceramic membranes are usually fabricated on porous ceramic substrates, using a repetitive coating‐sintering process to form a multilayered structure. This results in lengthy fabrication periods and high fabrication costs. In this work, we developed a novel fabrication process, melding, by combining vacuum infiltration and pore tuning techniques to directly construct the ceramic membrane layer within the porous ceramic substrate. By careful selection of powder sizes, the detrimental penetration effect can be modified into a benefit, forming an ultrathin membrane layer with thickness less than 1.45 µm after sintering at 1200°C. Compared favorably with dip‐coated ceramic membranes, the melded ceramic membrane had much smaller nominal pore sizes (0.19 vs 0.31 µm), but much higher water permeance (>60%). The melded ceramic membrane also had the highest rejection (98.5%) toward 125 nm polystyrene latex suspensions (2 ppm), highest sustained oil removal efficiency (>90%) under oil‐in‐water emulsion (200 ppm) filtration, and the least irreversible fouling (<8.6%). The melding process also significantly reduced the raw powders required, leading to an 86% reduction in material costs, as compared to the multilayered ceramic membranes.

Drying of water from porous structures investigated by time-resolved X-ray tomography

In this contribution, we apply time-resolved X-ray tomography to study drying of water in porous ceramic substrates used in emission control technologies. A time resolution of 2 s is achieved, and allows to observe the spatiotemporal distribution of water in structured porous materials. An image processing framework based on machine learning is introduced to track pore emptying and filling in a large number of 3D scans. Drying curves are extracted from the tomographic data to investigate drying in materials with different structural properties. Water redistribution by capillary pumping and rapid pore emptying by Haines jumps are observed, and their impact on drying dynamics is discussed. The relationship between the evolution of water clusters and different drying regimes is established. The obtained information on the interplay between pore emptying, water redistribution and the size of water clusters provides an important link between the structural properties of dried materials and their drying rate.

Layer-by-layer assembly of nanocomposite interlayers on a kaolin substrate for enhancing membrane performance of Pb(II) and Cd(II) removal

Developing an ultra-thin polyamide selective layer with sufficient mechanical robustness on a highly porous ceramic substrate is challenging for removing heavy metal ions from wastewater. We synthesized a reliable ceramic-polyamide membrane by assembling nanocomposite interlayers of alumina and carbon black on the kaolin substrate. The surface morphology, pore size distribution, and roughness of ceramic substrates were improved by introducing the nanocomposite interlayer. The corresponding optimized water flux, Pb(II), and Cd(II) removal efficiency are 2.75 L m−2 h−1, 98.44%, and 97.51%, respectively, which are better than those of the polyamide films constructed directly on the ceramic substrate. This facile structure provides more active sites for forming ultrathin polyamide layers with satisfactory mechanical robustness. This paper provides a new perspective for fabricating efficient heavy metal ions filters.

Localized conversion of ZnO nanorods for fabricating Metal-Organic framework MAF-5 membranes for hydrogen separation

For the first time, a homologous metal oxides induced approach was used to fabricate MAF-5 membrane for small molecule separation systems. A continuous and dense MAF-5 membrane was well formed on a porous ceramic substrate by the localized conversion of a thinlayer of ZnO nanorods. The ZnO nanorods layer acting as an intermediate plays a multifunctional role in the formation of the high-quality MAF-5 membrane: (1) modifying the porous substrate to make it more smooth and even; (2) inducing the nucleation and growth of MAF-5 membrane; (3) connecting the MAF-5 membrane and substrate tightly to avoid the membrane peeling off. The as-prepared membrane was characterized by various techniques and proved that the membrane is continuous and high-quality. The excellent gas permeation performance for the MAF-5 membrane was achieved for single gases. The ideal selectivities were as high as 80.2, 87.1 and 105.7 for H2/CO2, H2/N2 and H2/CH4, respectively, which are far higher than their corresponding Knudsen diffusion values. It is therefore believed that the MAF-5 membrane is of potential application in the field of some small-molecular gas separation through a molecular sieving effect.

Obtaining and electronic emission of planar structures of metallic copper on a porous ceramic substrate

Planar structures of metallic copper are synthesized in porous glass (PG) plates by reduction of two-dimensional layers of copper (II) oxide by molecular hydrogen. The stability and electrical conductivity of the formed copper ensemble, close to the monolayer, are achieved when it fills the surface of the PG and is determined by the content and reduction temperature of the oxide precursor. The content of experimentally obtained copper oxide in porous glass is determined by its resistance to oxidation in air. A manifestation of the characteristic planar state of copper in porous glass is a slight slope of the dependences R(T–1). Te obtained values of the thermal coefficient of resistivity are in the range of 0.0005÷0.0008 degrees–1, which corresponds to values smaller than ones for bulk copper (0.004 degrees–1). Therefore, the formation of dielectric gaps resulting from the incomplete oxidation process for the twodimensional copper layer leads to an increase in the resistance while maintaining the adjacent sections, which in this case determine the nature of the conductivity, similar to metals. The occurrence of emission from the surface of Cu/PG systems is observed at values of the electric field strength less than 2 V/μm, decreasing in a narrow range when the copper content exceeds the conditional monolayer.The work was carried out within the framework of the state task with the financial support of the Ministry of Education of the Russian Federation (project No. FSZN-2020-0026).

Investigation of photocatalytic properties of TiO2 nanoparticle coating on fly ash and red mud based porous ceramic substrate

Titanium dioxide is one of the best semiconducting photocatalysts available for photocatalytic cleaning applications. Especially nano-sized TiO2 particles deposited on porous substrates can be utilized as a filter for solid and liquid media. On the other hand, red mud and thermal plant fly ash are hazardous wastes that are produced in large quantities. Recycling/reuse of these waste material in a porous ceramic production would be beneficial both for environmental and economical issues. In the present study, a porous substrate was produced from red mud and fly ash with varying ratios and additives of H3BO3, CaCO3, and MgCO3 for lowering the melting temperature and porosity formation. Sintered ceramics were then coated with nano-sized TiO2 particles by the sol-gel method. Ultrasonic dispersion of nano-sized TiO2 nanoparticles was also utilized as an alternative method for impregnation of nanoparticles into the porous structure of the ceramic substrate. Finally, photocatalytic activities and degradation of methylene blue (MB) under UV radiation of substrates were investigated. According to the SEM investigations, the sol-gel method was observed to be a better way of nanoparticle deposition because deposited particles are homogenous throughout the ceramic body. Also, this method provides lower particle sizes than the ones that were deposited by the ultrasonic dispersion method. This results in higher surface area and better photocatalytic activities.