CaTiO3 Research Articles

Production of calcium and magnesium titanates using concentrated solar energy

Solar energy is an adequate technology for different processes in metallurgy, materials processing, recycling, or ceramic-refractory materials, because of the high temperatures attained which are reached when the solar radiation is concentrated. This growing interest has also emerged from the obtaining of such temperatures without releasing pollutants such as carbon dioxide, SOx, NOx, or dioxins. Other benefits associated with concentrated solar energy are that this energy source is virtually free and the possibility of operating in places isolated from the electrical grid. Therefore, this research proposes the integration of concentrated solar energy in the production of calcium and magnesium titanates, which are materials with increasing demand in the field of electric components. Experimental work was carried out in the Odeillo solar furnace located in Font-Romeu-Odeillo-Via (France) using a 1.5-meter parabolic concentrator and mixtures of CaO and TiO2 and MgO and TiO2 in 1:1 molar ratio. Mixtures were subjected to values of incident radiation exceeding 900 W/m2 without using any special atmosphere and in very short times, which did not surpass 10 minutes. X-ray diffraction technique was employed to confirm the formation of the CaTiO3 and MgTiO3 perovskites. Therefore, concentrated solar energy might be a novel, fast, and environmentally sustainable manner of producing calcium and magnesium titanates.

Exploring Alkali Hydroxide Influence on Calcium Titanate Formation for Application in Biodiesel Catalysts

Biodiesel has been recognized as the most widely utilized biofuel around the world due to its significant role in reducing the consumption of crude oil and lowering environmental pollution levels. By serving as a renewable alternative to fossil fuels, bioethanol helps decrease greenhouse gas emissions and contributes to a more sustainable energy future. Traditionally, alkali hydroxides like NaOH and KOH have been mainstays in biodiesel synthesis. However, their overuse can lead to unwanted byproducts and operational complexities. Since calcium titanate can occur at a strong base condition, it presents an alternative avenue worth exploring. In this study, we investigate the influence of alkali hydroxides, namely LiOH, NaOH, and KOH, on the formation of calcium titanate through hydrothermal methods, with varying heating times. We aim to understand how different hydroxides affect the synthesis process and the resultant properties of calcium titanate. We delve into the vibrational properties of Ca‒O‒Ti and Ti‒O bonds using Fourier transform infrared spectroscopy (FTIR), confirming the presence of calcium titanate (JCPDS No.42-0423) through X-ray diffractometry (XRD). This thorough characterization provides insight into the structural integrity and composition of the synthesized materials. Moreover, scanning electron microscopy (SEM) reveals the intriguing cube-like morphology of calcium titanate, offering visual evidence of its unique structure. The fatty acid methyl ester Iimpressively, our results show that calcium titanate synthesized in 7 M NaOH and KOH solutions, heated for 24 hours, emerges as a promising biodiesel catalyst. We observe fatty acid methyl ester provides the percentages of 63.67% and 90.02%, respectively, indicating the catalytic efficacy of these materials in biodiesel production. These findings not only contribute to the understanding of calcium titanate synthesis but also pave the way for a sustainable future in biodiesel production by introducing efficient and eco-friendly catalysts.

Application and Research Progress of Perovskite in the Field of Optoelectronic Materials

Perovskite refers to a class of materials with the formula of ABO3. These oxides were first discovered in calcium titanate compounds. Perovskite materials have attracted widespread attention in the field of contemporary photovoltaic research due to their excellent photovoltaic properties, heralding their potential as protagonists of a new generation of photovoltaic materials. Nevertheless, the stability of perovskite materials needs to be enhanced. In addition, reducing the toxicity of the materials is a key challenge in advancing their commercialization. Currently, the rapid development of perovskite in the field of optoelectronics and its unique combination of properties have laid a solid foundation for its position as a mainstream optoelectronic material of the future. Therefore, this work focuses on the properties and applications of perovskite optoelectronics. With deeper scientific research and technological innovation, perovskites have the potential to overcome existing limitations and move towards large-scale commercial production. In the future, the further application of perovskite optoelectronic materials would have far-reaching implications for the global energy transition and environmental protection.

Structural, Microstructural, Dielectric and Ac-conductivity of CaTi1-xFexO3 Multiferroic Materials Synthesized by Solid State Method

In this study, the structural, microstructural, dielectric and conductivity properties of Fe-doped CaTiO3 (CT) ceramic were investigated. These ceramics were successfully synthesized using the conventional solid-state method. The X-ray diffraction and Rietveld refinement results showed that the ceramics at x=0.0, 0.1, 0.2 and 0.3 crystalized in the orthorhombic phase with the Pmmm space group. While for x=0.4, 0.5 and 0.6, the phase formation changes from orthorhombic to tetragonal phase with P4/mmm group space. The SEM results revealed a semi-spherical shape of grain for lower Fe content (≤0.4), while at x=0.5 and 0.6 an agglomeration phenomenon is observed and the observed density of the sample at x=0.5 is higher than the other ceramics. The dielectric properties were studied as function of frequency and temperature. The dielectric permittivity (ɛ’r) decreases as function of frequency at lower frequency region and remain almost independent of frequency at high frequency region in the whole temperature range of R.T–520 °C. Each converges at high frequency (>105 Hz) for all the temperatures. The evolution of ɛ’r as function of temperature for pure CT ceramic showed a stability at large range of temperature (from R.T to 250°C). For substituted ceramics, we obtained a phase transition which shifted to the lower temperature with the increase of Fe content. And the value of ɛ’r, increases for Fe-doped CT ceramics and reaches a maximal value for x=0.5 which is 50 time bigger than the pure ceramic. The AC conductivity, σAC, is found to increase rapidly as a function of frequency, at low frequency region, and increases linearly at high frequency region, which confirms the hopping of electrons related to the conduction mechanism. The σAC evolution is found to follow the Jonscher’s law and the s exponent decreased with the increasing temperature which is related to the correlated barrier height (CBH) model. And the σAC values increase with the increases of Fe content.

Time-Dependent Electrical Active and Ultrasound-Responsive Calcium Titanate Implant Coating with Immunomodulation, Osteogenesis, and Customized Antibacterial Activity.

Surgical site infection and insufficient osseointegration are notable risks factors associated with oral implant surgery. In this study, the development of a polarized calcium titanate (CT-P) coating for titanium surfaces is proposed as a solution to these problems. The coating generated electrical stimulation (ES) can inhibit pro-inflammatory M1-type macrophage polarization and promote anti-inflammatory M2-type macrophage polarization, resulting in favorable bone immunomodulation. The ES generated by the coating can match the physiological electrical potential that will change during bone repair, thereby promoting osseointegration in vivo. In addition, the system can also achieve on-demand antibacterial activity, mainly depending on the CT-P coating responding to ultrasound (US) irradiation to produce reactive oxygen species (ROS) and remove Staphylococcus aureus (S. aureus) on the surface of the implant. In conclusion, this work provides valuable insights for the development and clinical application of highly efficient electroactive coatings, as well as novel solutions for the selective treatment of bacterial infections in the surgical area.

Dielectric properties and energy storage performance of lead-free strontium calcium titanate (Sr0.60Ca0.40)TiO3 thick films

Dielectric properties and energy storage performance of lead-free strontium calcium titanate (Sr0.60Ca0.40)TiO3 thick films

Exploring the Role of Titanate Perovskites in the Oxidation of Amines to Imines via Photocatalysis.

Considering that structural differences could affect the photocatalytic efficiency of titanate perovskites, cubic SrTiO3 (STO) and tetragonal CaTiO3 (CTO) were synthesised as models to elucidate the structure-activity relationship. STO and CTO materials were produced through hydrothermal approaches, adjusting parameters such as temperature and pressure to optimise material purity. Among the perovskite photocatalysts, two stand out for their exceptional photocatalytic capacity and crystalline purity: CaTiO3, prepared at 180 ºC for 36 h, and SrTiO3, synthesised at 200 ºC for 24 h. Notably, we explore the selective ability of these materials for the photocatalytic oxidative self-coupling of benzylamine (BZA) to produce N-benzylidenebenzylamine (BZI), with CaTiO3 emerging as the most efficient catalyst for this reaction. The CTO material prepared at 180 ºC for 36 h (CTO180T-36) achieved a peak BZI production of 0.5 mM, with a total conversion of BZA after 7 h of irradiation. This study also emphasises the crucial role of reaction conditions and perovskite morphologies in fine-tuning photocatalytic performance. These findings highlight opportunities for developing efficient and selective photocatalytic processes, holding the compromise for applications in organic synthesis and sustainable green chemistry.

Photocurrent‐Directed Immunoregulation Accelerates Osseointegration through Activating Calcium Influx in Macrophages

AbstractEarly osteoimmune microenvironment disorder at the interface between bone and implant can lead to implant loosening, which prolongs patient convalescence, exacerbates postoperative complications, and potentially results in implant failure. The timely regulation of macrophages primarily orchestrates the entire long‐term regeneration process. Here, it is proposed to precisely direct macrophage polarization using localized photoelectrical signals generated by an excitable surface in response to remote stimulation via near‐infrared light (NIR). The photocurrent generated from the n–n heterojunction between calcium titanate (CaTiO3) and defective titanium dioxide (TiO2‐Vo) on the excitable surface can accurately direct macrophage polarization, suppressing acute inflammation at the early stage of post‐implantation and establishing a favorable osteoimmune microenvironment that promotes bone‐to‐implant integration. Mechanistic study reveals that photoelectric signals initiate increased calcium influx via voltage‐gated calcium ion channels, subsequently modulating calcium/calmodulin‐dependent protein kinase kinase 2 (Camkk2) and calcium/calmodulin‐dependent protein kinase I (Camk1) expression to regulate macrophage polarization. This optimization of the osteoimmune microenvironment results in enhanced mesenchymal stem cells (MSCs) recruitment and osteogenesis, ultimately accelerating bone‐to‐implant integration within 14 days post‐implantation. This research presents a novel method for adjusting in vivo spatiotemporal immune responses through the use of noninvasive and externally‐controlled targeted stimulations.

Calcium titanate corrosion inhibitor enabling carbon as inert anode for oxygen evolution in molten chlorides

The corrosion inhibition efficacy of titanate (CaTiO3) for carbon anodes in molten salts was investigated through various analytical techniques, including linear sweep voltammetry, X-ray diffraction, scanning electron microscopy, and energy dispersion spectroscopy. The results demonstrate that the addition of CaTiO3 corrosion inhibitor efficiently passivates the carbon anode and leads to the formation of a dense CaTiO3 layer during the electrolysis process in molten CaCl2−CaO. Subsequently, the passivated carbon anode effectively undergoes the oxygen evolution reaction, with an optimal current density for passivation identified at 400 mA/cm2. Comprehensive investigations, including CaTiO3 solubility tests in molten CaCl2−CaO and numerical modeling of the stability of complex ionic structures, provide compelling evidence supporting “complexation−precipitation” passivation mechanism. This mechanism involves the initial formation of a complex containing TiO2·nCaO by CaTiO3 and CaO, which subsequently decomposes to yield CaTiO3, firmly coating the surface of the carbon anode. In practical applications, the integration of CaTiO3 corrosion inhibitor with the carbon anode leads to the successful preparation of the FeCoNiCrMn high-entropy alloy without carbon contamination in the molten CaCl2−CaO.

Polarization of Lanthanum-Doped HA and Barium Calcium Titanate (BCT) Composites Exhibit Enhanced Osteoblast Activities and Antibacterial Properties

Polarization of Lanthanum-Doped HA and Barium Calcium Titanate (BCT) Composites Exhibit Enhanced Osteoblast Activities and Antibacterial Properties

Thermoluminescence response of Ce doped CaTiO3 nanophosphor synthesized by hydrothermal method for gamma dosimetry

Abstract Nanocrystalline calcium titanate (CaTiO3) doped with cerium ions (0.02 mol%) was synthesized via hydrothermal method and its luminescent properties were studied for gamma dosimetry. For the synthesized samples, the best luminescent response was achieved after annealing at 700 °C for 8 h. The synthesis was confirmed via XRD technique yielding the cyrstallite size of 22 nm for the most intense peak (121). The surface morphology was studied via scanning electron microscopy (SEM) yielding the grain size of 12 µm. The strong IR absorptions appeared at 700 cm−1 and 712 cm−1 attributed to bending mode of vibrations changing angle between Ti–O–Ti for CaTiO3 and CaTiO3:Ce respectively, as confirmed via Fourier-Transform Infrared (FTIR) Spectroscopy. Thermoluminescent (TL) response of undoped and doped samples was studied by Mikrolab RA94 TLD Reader-Analyzer having heating rate 10 °C/s, for absorbed doses 0–20 mGy from 137Cs γ-source having a dose rate 100 mSv/h. The found values at 662 keV for the photon-sensing parameters, i.e., mass attenuation coefficients (μ/ρ), mass-energy attenuation coefficient (μ en/ρ), effective atomic number for photon interaction (Z eff,PI) and effective atomic number for total photon energy absorption (Z eff,PEA) were 0.07030882 cm2/g, 0.0280245 cm2/g, 13.9 and 13.4 respectively. Thus, synthesized nanophosphor has shown excellent thermoluminescent dosimetric response for gamma radiation sensing in the selected dose range.

High thermal stability of the microwave dielectric properties of ZnNb2O6 with CaTiO3 addition

This paper presents a study of the dielectric properties of ZnNb2O6 (ZNO) with added CaTiO3 (CTO) in the microwave (MW) region. An X-ray diffraction analysis is performed, and a reaction between ZNO and CTO is demonstrated that results in the formation of other crystalline phases. The dielectric properties in the MW region show no significant change in permittivity (ε'r), whereas the addition of CTO results in an increase in the dielectric loss (tan δ). The thermal stability is also measured, and the temperature coefficient of resonant frequency (τf) is varied from −88.95 to −8.16 ppm °C−1. Numerical simulations are carried out to evaluate these materials for use as a dielectric resonator antenna, and the results show a reflection coefficient (|S11|) of below −10 dB, a radiation efficiency above 96 %, a bandwidth ranging from 100 to 170 MHz, and a gain of above 4.50 dBi. The values obtained here show that these materials could be employed in electronic devices acting in the C- and S-bands.

Prominent cycling reversibility and kinetics enabled by CaTiO3 protective layer on Zn metal for aqueous Zn-ion batteries

Aqueous Zn-ion batteries (AZIBs) have received considerable attention owing to their various advantages such as safety, low cost, simple battery assembly conditions, and high ionic conductivity. However, they still suffer from serious problems, including uncontrollable dendrite growth, corrosion, hydrogen evolution reaction (HER) from water decomposition, electrode passivation, and unexpected by-products. The creation of a uniform artificial nanocrystal layer on the Zn anode surface is a promising strategy for resolving these issues. Herein, we propose the use of a perovskite CaTiO3 (CTO) protective layer on Zn (CTO@Zn) as a promising approach for improving the performance of AZIBs. The CTO artificial layer provides an efficient pathway for Zn ion diffusion towards the Zn metal because of the high dielectric constant (εr = 180) and ferroelectric characteristics that enable the alignment of dipole moments and redistribute the Zn2+ ions in the CTO layer. By avoiding the direct contact of the Zn anode with the electrolyte solution, the uneven dendrite growth, corrosion, parasitic side reactions, and HER are mitigated, while CTO retains its mechanical and chemical robustness during cycling. Consequently, CTO@Zn demonstrates an improved lifespan in a symmetric cell configuration compared with bare Zn. CTO@Zn shows steady overpotential (∼68 mV) for 1500 h at 1 mA cm−2/0.5 mA h cm−2, excelling bare Zn. Moreover, when paired with the V2O5-C cathode, the CTO@Zn//V2O5-C full battery delivers 148.4 mA h g−1 (based on the mass of the cathode) after 300 cycles. This study provides new insights into Zn metal anodes and the development of high-performance AZIBs.

Preparation of Calcium Titanate Perovskite Compound, Optical and Structural Properties

In this work, we have successfully fabricated a calcium titanate perovskite compound. The resulting CaTiO3 compound was studied by preparing samples by compacting it in a powder state and using a Pousson device. The distance between the planes dhkl, Miller indices (hkl), degree of crystallinity and amorphism, structure and lattice parameters of the calcium titanate perovskite compound were determined using an X-ray diffractometer. Also, according to the results of FT-IR analysis, the formation of CaTiO3 perovskite is confirmed as a result of the study of molecular vibrations. The main broad peaks are observed in the range of 680÷400 cm-1, the absorption band at the wave number of 543,93 cm-1 corresponds to the specific stretching vibrations of Ti-O bonds and indicates the formation of the CaTiO3 perovskite type structure implies. Based on the results of these measurements, it will be possible to use semiconductor compounds in the future to create nanofilms by magnetron sputtering.

CaTiO3-rich precipitates and their impacts on ferroelectric domains during heating in (Ba,Ca)TiO3 ceramics

CaTiO3-rich precipitates and their impacts on ferroelectric domains during heating in (Ba,Ca)TiO3 ceramics

Are we approaching the development of a novel calcium phosphate-based bioceramic dental material?

ObjectivesDevelop a sustainable bovine hydroxyapatite dental ceramic with the addition of titanium dioxide (TiO2) nanoparticles (5 % and 8 % by weight), analyzing the outcome of this addition to the microstructure, as well as its mechanical and chemical properties, in order to evaluate whether they satisfy the International Organization for Standardization (ISO) 6872:2015 for dental ceramics or not. MethodsDisks were obtained through uniaxial followed by isostatic pressing from bovine hydroxyapatite powder and TiO2 nanoparticles and sintered at 1300ºC for 2 h. Three experimental groups were developed (HA, HA+5 %TiO2 and HA+8 %TiO2) and subjected to X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), indentation fracture (IF), biaxial flexural strength (BFS) and chemical solubility test. ResultsXRD revealed, for HA group, the appearance of a peak corresponding to b-tricalcium phosphate (ß-TCP). For HA+ 5 %TiO2 and HA+ 8 %TiO2, the entire composition was converted into ß-TCP and calcium titanate (CaTiO3). The SEM images showed a dense ceramic matrix and a uniform distribution of another phase in groups with TiO2 nanoparticles. HA+ 5 %TiO2 (1.40 ± 0.18 MPa.m1/2) and HA+ 8 %TiO2 (1.32 ± 0.18 MPa.m1/2) showed significantly higher fracture toughness values than HA (0.67 ± 0.09 MPa.m1/2). HA showed significantly higher characteristic stress (295.8 MPa) in comparison to groups with 5 % (235.1 MPa) and 8 % (214.4 MPa) TiO2 nanoparticles. Differences were not observed between the Weibull modulus values. The solubility results indicated that all experimental ceramics were above the 2000 ug/cm2 limit set by the ISO 6872:2015. SignificanceThis study proposed the development and characterization of a new ceramic for dental prosthesis made from HA extracted from bovine bones, with the intention of reusing these solids waste and transforming them into a sustainable and low-cost material. Although the experimental calcium phosphate ceramic with additions of 5 % and 8 % of TiO2 achieved desirable mechanical properties, the chemical solubility values were very high.

Preparation and characterization of nano‐filled polypropylene dielectric films

AbstractModified copper calcium titanate (MCCTO) or functional activated carbon (FANC) particles were added to functional polypropylene (FPP) or heat‐treated polypropylene (HTFPP) matrix to improve the performance of FPP as dielectric films. By testing and characterizing the prepared FPPwxMCCTOy, FPPwxFANCz, FPPwxMCCTOyFANCz and HTFPPwxMCCTOy, HTFPPwxFANCy and HTFPPwxMCCTOyFANCz films, It is found that the dielectric constant and discharge energy density of each FPPwxMCCTOy, FPPwxFANCz, HTFPPwxFANCz and HTFPPwxFANCz films reach the maximum when the MCCTO and FANC loads are close to 8 and 6 wt% respectively. FPPwxMCCTO8FANCz and HTFPPwxMCCTO8FANCz series films also obtain the maximum dielectric constant and discharge energy density at FANC load approaching 6 wt%. The discharge energy density of HTFPPw86MCCTO8FANC6 film prepared properly is 3.2 J/cm3, which is more than 3 times higher than that of FPP. When MCCTO and FANC loads are ≦8 and 6 wt% respectively, with the increase of additive content, More dense distribution of MCCTO and FANC was observed in FPPwxMCCTOy(or HTFPPwxMCCTOy), FPPwxFANCz(or HTFPPwxFANCz) and FPPwxMCCTO8FANCz(or HTFPPwxMCCTO8FANCz) series film sections. In this paper, we propose possible explanations for the apparent improvement in dielectric constant, discharge energy density and heat resistance of capacitive films after appropriate heat treatment or addition of appropriate MCCTO and/or FANC loads.

Copper doping induced band structure and morphology transformation in CaTiO3 for textile dye photodegradation applications

Semiconductor metal oxides with a wide bandgap like CaTiO3 can be exploited into an efficient visible light photocatalyst via cation doping. The type of dopant and the site of doping is known to greatly influence the photocatalytic activity of a material. Based on the intricacies of the density functional theory electronic structure study, we delve into the optimization of one-pot solvothermal synthesis to obtain Cu doped CaTiO3 nanocuboids. Doping of copper not only resulted in change in the electronic structure of the material but also led to change in the morphology. The uneven nanostep architecture resulted in increase in the surface area of the catalyst, which led to more active sites for the adsorption of the dyes and subsequent degradation. The reduced band gap and decreased recombination of charge carriers made the copper doped calcium titanate an efficient photocatalyst for degradation of both cationic (99.7% degradation of MV dye in 120 minutes) and anionic (99.8% degradation of RB in 45 minutes) dyes.

CaTiO3 nanoparticles as functional additives for the BaTiO3-based X8R type dielectric ceramics

This research investigates the potential of Calcium titanate (CaTiO3 or CT) nanoparticles as functional additives to enhance the dielectric properties of Barium titanate (BaTiO3 or BT)-based ceramic dielectrics. To address the need for high-temperature stability in MLCC (multilayer ceramic capacitor) applications, especially within the automotive and aerospace sectors, we have explored BT-based complex perovskite solid solutions comprising various cation substitutions, including Ca2+ and Yb3+, into barium titanate (BT) as a method to suppress the dielectric property anomaly near the Curie temperature effectively. The focus is on the impact of the application of CT nanoparticles as additive materials on phase formation, microstructure development, and dielectric behavior of the resulting ceramics to align with the Extended 'Temperature Coefficient of Capacitance (TCC)' criteria defined by the EIA X8R specification. When the hydrothermally synthesized CT nanopowder was applied in the Ca-doped BT ceramics fabrications as source material of the Ca dopants, it was beneficial to achieve both temperature stability and high dielectric constant. The CT nanoparticles are believed to play multiple roles during the solid-state reaction with BT and rare earth dopant (Yb). Since the Yb3+ ions can be more easily dissolved into the CT lattice than BT with their amphoteric character, the CT nanoparticles in the BT-CT-Yb2O3 mixture can act as an intermediary, dissolving the Yb3+ first in its A- or B-site before the final solid-solution formation with the BT. The sequential substitutions of the Yb3+ and Ca2+ into BT via CT nanoparticles could affect the site occupancy of Ca2+ in the BT lattice, which is very important in determining the dielectric properties of the Ca-doped BT processed in reducing atmospheres. Through a comprehensive experimental approach, including phase composition analysis via X-ray diffraction (XRD) and microstructural examination using Field Emission Scanning Electron Microscopy (FE-SEM) and Transmission Electron Microscopy (TEM), this work reveals the significance of synthetic methodology and dopant incorporation strategy on achieving a desired core-shell microstructure and improved dielectric performance. This research underscores the efficacy of CT nanoparticles as a promising route towards the development of BT-based dielectric ceramics with superior temperature stability, offering valuable insights for the advancement of MLCC technology to cater to high-temperature applications.

Effect of Operating Parameters on Photocatalytic Treatment of Synthetic Wastewater Using CaTiO3

Photocatalysis is thought to be a long-term, environmentally friendly, economically feasible, and promising technique for treating wastewater. The development of semiconductor nanoparticles has generated a great deal of interest in the treatment of wastewater. To break down complex contaminants found in wastewater into simpler compounds, including H2O and CO2, several UV/visible light excitable nanomaterials have been explored as photocatalysts. Their effectiveness can be managed by adjusting several reaction-related parameters like the intensity of light, irradiance time, pH, catalyst dose, temperature, doping, etc. The performance of the photocatalyst in the photodegradation of contaminants is greatly affected by these parameters. The main goal of this study is to find the best operational parameters and their impact on the photocatalytic treatment of synthetic waste-water using calcium titanate (CaTiO3) nanoparticles. For this purpose, sol-gel synthesized CaTiO3 with a band gap of 3.57 eV was used. The size of the synthesized nanoparticles is smaller than 47.62 nm. The results of photocatalytic treatment of synthetic wastewater demonstrate that CaTiO3 exhibits its best photocatalytic performance at 33 W UV light, pH 6.0, and 3.33 g L-1 CaTiO3 dose with 8 hours of irradiation time. With chemical oxygen demand (COD) concentrations varying from 700 to 40000 mg L-1 at the initial stages, the percentage of COD removal under these conditions was 100% to 77%.