A high-flux, photocatalytic wood-derived filter for high-efficiency water purification.

Wastewater purification has evolved into a global problem in the face of increasing scarcity of freshwater resources. Photocatalysis technology possesses prominent advantages in treating pollutants in water because of its low cost and mild reaction conditions, which provides an effective way to treat multiple pollutants and reduce membrane fouling. Herein, we combine photocatalysis technology with filtration technology via in situ reduction Bi0 with Bi2SiO5 strategy incorporating a carbonized wood filter to synthesize carbon/Bi2SiO5@Bi bi-functional composite. Thus, simultaneous filtration and photocatalytic degradation of Rhodamine B and tetracycline were achieved. After filtrating for 30 min, the degradation rate of RhB and TC were 94.23 % and 81.39 %, respectively. Especially, the flux of RhB and TC were up to 2162.16 L m-2 h-1 and 1811.32 L m-2 h-1. In addition, the composite filter also has good recyclability and reusability, after 5 cycles, the degradation efficiency of RhB remains at 91 %. This study utilized photocatalytic technology combined with membrane filtration technology to successfully solve the contradiction between catalytic efficiency and water flux, which realized rapid and dynamic removal of organic pollutants from water. Besides, the use of carbonized wood-based materials provides a potential biomass technology for the preparation of bifunctional photocatalytic filters.

The Influence of High-Energy Milling on the Phase Formation, Structural, and Photoluminescent Properties of CaWO4 Nanoparticles.

CaWO4 nanoparticles were obtained by facile mechanochemical synthesis at room temperature, applying two different milling speeds. Additionally, a solid-state reaction was employed to assess the phase composition, structural, and optical characteristics of CaWO4. The samples were analyzed by X-ray diffraction (XRD), transition electron microscopy (TEM), and Raman, infrared (IR), ultraviolet-visible (UV-Vis) reflectance, and photoluminescence (PL) spectroscopies. The phase formation of CaWO4 was achieved after 1 and 5 h of applied milling speeds of 850 and 500 rpm, respectively. CaWO4 was also obtained after heat treatment at 900 °C for 12 h. TEM and X-ray analyses were used to calculate the average crystallite and grain size. The Raman and infrared spectroscopies revealed the main vibrations of the WO4 groups and indicated that more distorted structural units were formed when the compound was synthesized by the solid-state method. The calculated value of the optical band gap of CaWO4 significantly increased from 2.67 eV to 4.53 eV at lower and higher milling speeds, respectively. The determined optical band gap of CaWO4, prepared by a solid-state reaction, was 5.36 eV. Blue emission at 425 (422) nm was observed for all samples under an excitation wavelength of 230 nm. CaWO4 synthesized by the solid-state method had the highest emission intensity. It was established that the intensity of the PL peak depended on two factors: the morphology of the particles and the crystallite sizes. The calculated color coordinates of the CaWO4 samples were located in the blue region of the CIE diagram. This work demonstrates that materials with optical properties can be obtained simply and affordably using the mechanochemical method.

Design and preparation of FeNiCoCrY high-entropy alloy nanopowders with sustained, efficient and rapid degradation properties of CR and Cr(VI) wastewater.

In this paper, magnetic nanopowders of Fe19.5Ni40Co19.5Cr19.5Y1.5 high-entropy alloy compositions were successfully prepared by the liquid phase reduction method, which represented a breakthrough from the traditional process of preparing high-entropy alloy nanopowders. The powders had a high specific surface area of 136.23 m2/g and exhibited sustained, efficient, and rapid degradation characteristics for high concentrations of CR and ultra-high concentrations of Cr(VI) wastewater. It was demonstrated that the removal rate of CR remained at 100 % after 100 cycles and 81 % of Cr after 8 cycles of the powder without changing the pH and room temperature. The powders also demonstrated good soft magnetic properties, which allowed them to be conveniently separated and recycled using magnetic field treatment, thus addressing the issue of recycling raw materials without causing secondary pollution in wastewater treatment. Furthermore, the analyzed powders also exhibited fast and efficient degradation effects.

Copper-doped magnesium phosphate nanopowders for critical size calvarial bone defect intervention.

Calvarial defects of bone present difficult clinical situations, and their restoration using biocompatible materials requires special treatments that enable bone regeneration. Magnesium phosphate (MgP) is known as an osteoinductive biomaterial because it contains Mg2+ ions and P ions that enhance the activity of osteoplast cells and help in bone regeneration. In this study, MgP and CuO-doped MgP were fabricated and characterized for their physicomechanical properties, particle size, morphology, surface area, antibacterial test, and in vitro bioactivity evaluation using the following techniques: X-rays diffraction, Fourier-transformer infrared, TEM, and Brunauer, Emmett and Teller (BET) surface area, X-rays photoelectron spectroscopy (XPS), and Scanning electron microscopy (SEM). Furthermore, these nanopowders were implanted in adult inbred male Wistar rats and studied after two periods (28 and 56 days). The results demonstrated that the obtained semiamorphous powders are in nanoscale (≤ 50 nm). XPS analysis ensured the preparation of MgP as mono MgP and CuO were incorporated in the structure as Cu2+ . The bioactivity was supported by the observation of calcium phosphate layer on the nanopowders' surface. The in vivo study demonstrated success of MgP nanopowders especially those doped with CuO in restoration of calvarial defect bone. Therefore, fabricated biomaterials are of great potential in restoration of bone calvarial defects.

A New Method for Tungsten Oxide Nanopowder Deposition on Carbon-Fiber-Reinforced Polymer Composites for X-ray Attenuation.

A new method for the synthesis and deposition of tungsten oxide nanopowders directly on the surface of a carbon-fiber-reinforced polymer composite (CFRP) is presented. The CFRP was chosen because this material has very good thermal and mechanical properties and chemical resistance. Also, CFRPs have low melting points and are transparent under ionized radiation. The synthesis is based on the direct interaction between high-power-density microwaves and metallic wires to generate a high-temperature plasma in an oxygen-containing atmosphere, which afterward condenses as metallic oxide nanoparticles on the CFRP. During microwave discharge, the value of the electronic temperature of the plasma, estimated from Boltzmann plots, reached up to 4 eV, and tungsten oxide crystals with a size between 5 nm and 100 nm were obtained. Transmission electron microscopy (TEM) analysis of the tungsten oxide nanoparticles showed they were single crystals without any extended defects. Scanning electron microscopy (SEM) analysis showed that the surface of the CFRP sample does not degrade during microwave plasma deposition. The X-ray attenuation of CFRP samples covered with tungsten oxide nanopowder layers of 2 µm and 21 µm thickness was measured. The X-ray attenuation analysis indicated that the thin film with 2 µm thickness attenuated 10% of the photon flux with 20 to 29 KeV of energy, while the sample with 21 µm thickness attenuated 60% of the photon flux.

Nexus Advances Using Marine Biopolymeric Gel Material as a Photocatalyst for the Oxidation of Agricultural Wastewater Containing Insecticides.

The attention of the research community is focused not only on waste elimination, but also on waste valorization. The natural marine biopolymer gel substance chitosan, which can be derived from the waste substances of marine life, is a polymer-matrix-based nanocomposite. Chitosan attracts special attention due to its potential applications, especially in wastewater treatment. In this regard, magnetite-incorporated chitosan powders of nanometer scale were synthesized by a simple co-precipitation method to attain the dual functions of chitosan gel and magnetite. The synthesized magnetite-incorporated chitosan nanopowders were verified using X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy, a vibrating-sample magnetometer (VSM), a scanning electron microscope (SEM), and transmission electron microscopy (TEM) images, which showed that the synthesized magnetite-incorporated chitosan was nanosized. The superior application of such a material to offset the deterioration of the environment caused by insecticides is attained through a photocatalytic reaction. The experimental results verified the function of magnetite-incorporated chitosan, since it increased the composite-specific surface area, resulting in high methomyl molecule oxidation. Methomyl oxidation reached almost complete insecticide removal (99%) within only one hour of irradiance time. The optimal operational conditions were investigated, and the maximal removal rate occurred when the aqueous solution was at an acidic pH of 3.0. The reaction was affected by differing hydrogen peroxide and catalyst doses, and the optimized reagent was recorded at the levels of 40 and 400 mg/L of catalyst and hydrogen peroxide, respectively. Also, catalyst reusability was attained, confirming its sustainability, since it could be used for successive cycles. From the current investigation, it is proposed that magnetite-chitosan nanoparticles could serve as a promising photocatalyst for the elimination of insecticides from wastewater in a green manner.

Long-Term Oxidation Susceptibility in Ambient Air of the Semiconductor Kesterite Cu2ZnSnS4 Nanopowders Made by Mechanochemical Synthesis Method.

The often overlooked and annoying aspects of the propensity of no-oxygen semiconductor kesterite, Cu2ZnSnS4, to oxidation during manipulation and storage in ambient air prompted the study on the prolonged exposure of kesterite nanopowders to air. Three precursor systems were used to make a large pool of the cubic and tetragonal polytypes of kesterite via a convenient mechanochemical synthesis route. The systems included the starting mixtures of (i) constituent elements (2Cu + Zn + Sn + 4S), (ii) selected metal sulfides and sulfur (Cu2S + ZnS + SnS + S), and (iii) in situ made copper alloys (from the high-energy ball milling of the metals 2Cu + Zn + Sn) and sulfur. All raw products were shown to be cubic kesterite nanopowders with defunct semiconductor properties. These nanopowders were converted to the tetragonal kesterite semiconductor by annealing at 500 °C under argon. All materials were exposed to the ambient air for 1, 3, and 6 months and were suitably analyzed after each of the stages. The characterization methods included powder XRD, FT-IR/UV-Vis/Raman/NMR spectroscopies, SEM, the determination of BET/BJH specific surface area and helium density (dHe), and direct oxygen and hydrogen-content analyses. The results confirmed the progressive, relatively fast, and pronounced oxidation of all kesterite nanopowders towards, mainly, hydrated copper(II) and zinc(II) sulfates, and tin(IV) oxide. The time-related oxidation changes were reflected in the lowering of the energy band gap Eg of the remaining tetragonal kesterite component.

Metal-Organic Frameworks and Their Derivatives-Based Nanostructure with Different Dimensionalities for Supercapacitors.

With the urgent demand for the achievement of carbon neutrality, novel nanomaterials, and environmentally friendly nanotechnologies are constantly being explored and continue to drive the sustainable development of energy storage and conversion installations. Among various candidate materials, metal-organic frameworks (MOFs) and their derivatives with unique nanostructures have attracted increasing attention and intensive investigation for the construction of next generation electrode materials, benefitting from their unique intrinsic characteristics such as large specific surface area, high porosity, and chemical tunability as well as the interconnected channels. Nevertheless, the poor electrochemical conductivity severely limits their application prospects, hence a variety of nanocomposites with multifarious structures have been designed and proposed from different dimensionalities. In this review, recent advances based on MOFs and their derivatives in different dimensionalities ranging from 1D nanopowders to 2D nanofilms and 3D aerogels, as well as 4D self-supporting electrodes for supercapacitors are summarized and highlighted. Furthermore, the key challenges and perspectives of MOFs and their derivatives-based materials for the practical and sustainable electrochemical energy conversion and storage applications are also briefly discussed, which may be served as a guideline for the design of next-generation electrode materials from different dimensionalities.

Comparative Study of MgO Nanopowders Prepared by Different Chemical Methods.

Magnesium oxide (MgO) was synthesized by three different methods: the sol-gel (SG), microwave-assisted sol-gel (MW), and hydrothermal (HT) methods for comparing the influence of the preparation conditions on the properties of the products. The powders were annealed at 450 °C. The samples were characterized by X-ray diffraction, scanning electron microscopy (SEM), transmission electron microscopy (TEM/HRTEM), selected area electron diffraction (SAED), energy-dispersive X-ray spectroscopy (EDX), BET specific surface area and porosity, photoluminescence, and UV-Vis spectroscopy. The samples consisted mainly of periclase as a crystalline phase, and the MW and HT preparation methods generated particles with higher specific surface areas. The powders had less-defined morphologies and high levels of aggregation. The optical band gaps of the samples were determined from UV DRS, and the photocatalytic activities of the magnesium oxides obtained by the three methods towards the degradation of methyl orange (MO) under UV light irradiation was evaluated.

Tunable, Wide-Temperature, and Macroscale Superlubricity Enabled by Nanoscale Van Der Waals Heterojunction-to-Homojunction Transformation.

Achieving macroscale superlubricity of van der Waals (vdW) nanopowders is particularly challenging, due to the difficulty in forming ordered junctions before friction and the friction-induced complex contact restructuration among multiple nanometer-sized junctions. Here, a facile way is reported to achieve vdW nanopowder-to-heterojunction conversion by graphene edge-oxygen (GEO) incorporation. The GEO effectively weakens the out-of-plane edge-edge and in-plane plane-edge states of the vdW nanopowder, leading to a coexistent structure of nanoscale homojunctions and heterojunctions on the grinding balls. When sliding on diamond-like carbon surfaces, the ball-supported structure governs macroscale superlubricity by heterojunction-to-homojunction transformation among the countless nanoscale junctions. Furthermore, the transformation guides the tunable design of superlubricity, achieving superlubricity (µ ≈ 0.005) at wide ranges of load, velocity, and temperature (-200 to 300 °C). Atomistic simulations reveal the GEO-enhanced conversion of vdW nanopowder to heterojunctions and demonstrate the heterojunction-to-homojunction transformation superlubricity mechanism. The findings are of significance for the macroscopic scale-up and engineering application of structural superlubricity.

Flexible Electromagnetic Shielding Nano-Composites Based on Silicon and NiFe2O4 Powders.

In this paper, the obtaining and characterization of five experimental models of novel polymer composite materials with ferrite nano-powder are presented. The composites were obtained by mechanically mixing two components and pressing the obtained mixture on a hot plate press. The ferrite powders were obtained by an innovative economic co-precipitation route. The characterization of these composites consisted of physical and thermal properties: hydrostatic density, scanning electron microscopy (SEM), and TG DSC thermal analyses, along with functional electromagnetic tests in order to demonstrate the functionality of these materials as electromagnetic shields (magnetic permeability, dielectric characteristics, and shielding effectiveness). The purpose of this work was to obtain a flexible composite material, applicable to any type of architecture for the electrical and automotive industry, necessary for protection against electromagnetic interference. The results demonstrated the efficiency of such materials at lower frequencies, but also in the microwave domain, with higher thermal stability and lifetime.

Erbium-Doped Lu2O3-MgO and Sc2O3-MgO IR-Transparent Composite Ceramics.

Novel IR-transparent ceramics of erbium-doped Lu2O3-MgO and Sc2O3-MgO composites have been successfully obtained using a combination of glycine-nitrate self-propagating high-temperature synthesis and vacuum hot-pressing methods. Composites have densities greater than 99.5% of those calculated by X-ray diffraction and consist of uniformly distributed submicron grains of magnesium and rare earth oxides. The transmittances of 1.5 mm thick composites are as high as 84.5% and 78.9% at ~5 µm for Er:Lu2O3-MgO and Er:Sc2O3-MgO, respectively. Both composites are favorable matrices for doping with erbium ions, which exhibit intense luminescence in the visible, near, and mid-IR under relevant excitation. The position of the luminescence bands is similar to Er:Lu2O3 and Er:Sc2O3 ceramics; the lifetimes of the 4I13/2 state are 8.85 ± 0.1 ms and 5.7 ± 0.2 ms for 3%Er:Lu2O3-MgO and 3%Er:Sc2O3-MgO, respectively.

Oxygen Aspects in the High-Pressure and High-Temperature Sintering of Semiconductor Kesterite Cu2ZnSnS4 Nanopowders Prepared by a Mechanochemically-Assisted Synthesis Method.

We explore the important aspects of adventitious oxygen presence in nanopowders, as well as in the high-pressure and high-temperature-sintered nanoceramics of semiconductor kesterite Cu2ZnSnS4. The initial nanopowders were prepared via the mechanochemical synthesis route from two precursor systems, i.e., (i) a mixture of the constituent elements (Cu, Zn, Sn, and S), (ii) a mixture of the respective metal sulfides (Cu2S, ZnS, and SnS), and sulfur (S). They were made in each system in the form of both the raw powder of non-semiconducting cubic zincblende-type prekesterite and, after thermal treatment at 500 °C, of semiconductor tetragonal kesterite. Upon characterization, the nanopowders were subjected to high-pressure (7.7 GPa) and high-temperature (500 °C) sintering that afforded mechanically stable black pellets. Both the nanopowders and pellets were extensively characterized, employing such determinations as powder XRD, UV-Vis/FT-IR/Raman spectroscopies, solid-state 65Cu/119Sn NMR, TGA/DTA/MS, directly analyzed oxygen (O) and hydrogen (H) contents, BET specific surface area, helium density, and Vicker's hardness (when applicable). The major findings are the unexpectedly high oxygen contents in the starting nanopowders, which are further revealed in the sintered pellets as crystalline SnO2. Additionally, the pressure-temperature-time conditions of the HP-HT sintering of the nanopowders are shown (in the relevant cases) to result in the conversion of the tetragonal kesterite into cubic zincblende polytype upon decompression.

Artemisinin Loaded Cerium-Doped Nanopowders Improved In Vitro the Biomineralization in Human Periodontal Ligament Cells.

BACKGROUND: A promising strategy to enhance bone regeneration is the use of bioactive materials doped with metallic ions with therapeutic effects and their combination with active substances and/or drugs. The aim of the present study was to investigate the osteogenic capacity of human periodontal ligament cells (hPDLCs) in culture with artemisinin (ART)-loaded Ce-doped calcium silicate nanopowders (NPs); Methods: Mesoporous silica, calcium-doped and calcium/cerium-doped silicate NPs were synthesized via a surfactant-assisted cooperative self-assembly process. Human periodontal ligament cells (hPDLCs) were isolated and tested for their osteogenic differentiation in the presence of ART-loaded and unloaded NPs through alkaline phosphatase (ALP) activity and Alizarine red S staining, while their antioxidant capacity was also evaluated; Results: ART promoted further the osteogenic differentiation of hPDLCs in the presence of Ce-doped NPs. Higher amounts of Ce in the ART-loaded NPs inversely affected the mineral deposition process by the hPDLCs. ART and Ce in the NPs have a synergistic role controlling the redox status and reducing ROS production from the hPDLCs; Conclusions: By monitoring the Ce amount and ART concentration, mesoporous NPs with optimum properties can be developed towards bone tissue regeneration demonstrating also potential application in periodontal tissue regeneration strategies.

Atmosphere-Assisted FLASH Sintering of Nanometric Potassium Sodium Niobate.

The request for extremely low-temperature and short-time sintering techniques has guided the development of alternative ceramic processing. Atmosphere-assisted FLASH sintering (AAFS) combines the direct use of electric power to packed powders with the engineering of operating atmosphere to allow low-temperature conduction. The AAFS of nanometric Potassium Sodium Niobate, K0.5Na0.5NbO3, a lead-free piezoelectric, is of great interest to electronics technology to produce efficient, low-thermal-budget sensors, actuators and piezo harvesters, among others. Not previously studied, the role of different atmospheres for the decrease in FLASH temperature (TF) of KNN is presented in this work. Additionally, the effect of the humidity presence on the operating atmosphere and the role of the compact morphology undergoing FLASH are investigated. While the low partial pressure of oxygen (reducing atmospheres) allows the decrease of TF, limited densification is observed. It is shown that AAFS is responsible for a dramatic decrease in the operating temperature (T < 320 °C), while water is essential to allow appreciable densification. In addition, the particles/pores morphology on the green compact impacts the uniformity of AAFS densification.

Fabrication of strong bioresorbable composites from electroexplosive Fe-Fe3O4 nanoparticles by isostatic pressing followed by vacuum sintering.

Bulk samples with high mechanical strength reaching 1000 MPa were obtained from electroexplosive Fe-Fe3O4 nanoparticles containing 81 wt. % Fe. Maximum strength is achieved by consolidation of the nanoparticles by isostatic pressing followed by vacuum sintering at 700 °C. A further increase in the sintering temperature leads to the formation of large pores with a size of up to 5 µm and an intense interaction of Fe and Fe3O4 with the formation of FeO leading to the embrittlement of the samples and a decrease in their strength. The degradation rate of Fe- Fe3O4 samples in NaCl (0.9% wt.) and Hank's solution is 7 times higher than that of samples obtained by sintering an electroexplosive Fe nanopowder under the same conditions.

Wettability of Nanostructured Transition-Metal Oxide (Al2O3, CeO2, and AlCeO3) Powder Surfaces.

Wettability has been the focal point of many studies in metal oxide materials due to their applications in water-gas shift reactions, organic reactions, thermochemical water splitting, and photocatalysis. This paper presents the results of systematic experimental studies on the wettability of surfaces of nanostructured transition-metal oxides (TMOs) (Al2O3, CeO2, and AlCeO3). The wettability of nanoparticles was investigated by measuring contact angles of different concentrations of water-based nanofluids (0.05-0.1 wt%) on the glass slide. The morphology, the heterostructure, and the nature of incorporated nanoparticles were confirmed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Characteristic diffraction patterns of the nanomaterials were evaluated using energy-dispersive X-ray spectroscopy (EDS) and X-ray diffraction (XRD) techniques. The contact angles of water-Al2O3, water-CeO2, and water-AlCeO3 were measured as 77.5 ± 5°, 89.8 ± 4°, and 69.2 ± 1°, respectively. This study suggests that AlCeO3 is strongly water-wet (hydrophilic), while CeO2 is weakly water-wet (hydrophobic). It further demonstrated that the sizes and compositions of the nanoparticles are key parameters that influence their wetting behaviors.

Barium Oxide Doped Magnesium Silicate Nanopowders for Bone Fracture Healing: Preparation, Characterization, Antibacterial and In Vivo Animal Studies.

Magnesium silicate (MgS) nanopowders doped with barium oxide (BaO) were prepared by sol-gel technique, which were then implanted into a fracture of a tibia bone in rats for studying enhanced in vivo bone regeneration. The produced nanopowders were characterized using X-ray diffraction (XRD), Fourier transform infrared spectra (FTIR), scanning electron microscope with energy-dispersive X-ray spectrometry (SEM-EDX) and transmission electron microscope (TEM). Mechanical and bactericidal properties of the nanopowders were also determined. Increased crystallinity, particle diameter and surface area were found to decrease after the BaO doping without any notable alterations on their chemical integrities. Moreover, elevated mechanical and antibacterial characteristics were recognized for higher BaO doping concentrations. Our animal studies demonstrated that impressive new bone tissues were formed in the fractures while the prepared samples degraded, indicating that the osteogenesis and degradability of the BaO containing MgS samples were better than the control MgS. The results of the animal study indicated that the simultaneous bone formation on magnesium biomaterial silicate and barium MgS with completed bone healing after five weeks of implantations. The findings also demonstrated that the prepared samples with good biocompatibility and degradability could enhance vascularization and osteogenesis, and they have therapeutic potential to heal bone fractures.

Size-Dependent Magnetic and Magneto-Optical Properties of Bi-Doped Yttrium Iron Garnet Nanopowders.

Bi-doped yttrium iron garnet nanopowders were successfully synthesized by a combustion method at different synthesis conditions, and the evolution of their structural, magnetic, and magneto-optical properties has been studied by various methods. X-ray diffraction analysis revealed that crystallite size increases with increase as in annealing time (tA) well as in annealing temperature (TA) and varied from 15.2 nm (TA = 650 °C, tA = 0.5 h) to 44.5 nm (TA = 800 °C, tA = 12 h). The magnetic hysteresis loops exhibit behavior characteristic of soft magnetic materials; herewith, the saturation magnetization demonstrates a growing trend with increasing crystallite size (D). The behavior of the coercivity indicates that, at room temperature, the transition between single-domain and multidomain states occurs at D = 35.3 nm. It was found that the size effect in the MCD spectra is clearly observed for the samples with crystallite sizes less than 42.2 nm for an intersublattice charge-transfer transition and a crystal-field tetrahedral transition. The influence of cation redistribution on the observed changes has been discussed.

Comparative Study of Polyethylene Films Embedded with Oxide Nanoparticles of Granulated and Free-Standing Nature.

Nanocomposite polymer films are a very diverse research field due to their many applications. The search for low-cost, versatile methods, producing regulated properties of the final products, has thus become extremely relevant. We have previously reported a bulk-scale process, dispersing granulated metal oxide nanoparticles, of both unary and multi-component nature, in a low-density polyethylene (LDPE) polymer matrix, establishing a reference in the produced films' optical properties, due to the high degree of homogeneity and preservation of the primary particle size allowed by this method. In this work, unmodified, free-standing particles, namely zinc oxide (ZnO), titanium dioxide (TiO2), aluminum oxide (Al2O3), and silicon dioxide (SiO2) are blended directly with LDPE, and the optical properties of the fabricated films are compared to those of films made using the granulation process. The direct blending process evidently allows for control of the secondary particle size and ensures a homogeneous dispersion of the particles, albeit to a lesser extent than the granulation process. Despite the secondary particle size being comparatively larger than its granulated counterpart, the process still provides a regulated degree of deagglomeration of the free-standing oxide particles, so it can be used as a low-cost alternative. The regulation of the secondary particle size tunes the transmission and reflection spectra, in both unary and mixed oxide compositions. Finally, the direct blending process exhibits a clear ability to tune the energy band gap in mixed oxides.