Browse
Submit Data
Databases
API
Help

Dataset Information

10 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Mechanism of Photodegradation of Organic Pollutants in Seawater by TiO₂-Based Photocatalysts and Improvement in Their Performance.

ABSTRACT: The mechanism of photodegradation of organic pollutants in seawater by TiO₂-based catalysts irradiated by visible light was first explored by adding holes and free radical traps. The results showed that the photogenerated holes formed by the catalyst played a key role in the degradation of organic pollutants, regardless of whether the photodegradation occurred in seawater or pure water. Considering that the Yb-TiO₂-rGO catalyst has a strong adsorption for organics, the salt ion almost did not interfere with the adsorption of pollutants by Yb-TiO₂-rGO. Therefore, the degradation performance of Yb-TiO₂-rGO did not remarkably change in the two water systems. For P25-ZN with a weak adsorption capacity for organics, several salt ions in the seawater hindered the contact of pollutants with the catalyst surface. Thus, the degradation rate of P25-ZN for phenol was significantly reduced. After the solvothermal reduction treatment for catalysts using ethylene glycol (EG) as the solvent, the increase in the Ti³⁺ content in the catalyst improved the visible-light response and activity of the catalyst. In addition, a small amount of EG grafted on the catalyst surface promoted the photocatalytic reaction process on the catalyst surface, thereby effectively resisting the interference of salt ions.

SUBMITTER: Xu H

PROVIDER: S-EPMC8600626 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Photodegradation of organic pollutants RhB dye using UV simulated sunlight on ceria based TiO2 nanomaterials for antibacterial applications.

Project description:To photo-catalytically degrade RhB dye using solar irradiation, CeO2 doped TiO2 nanocomposites were synthesized hydrothermally at 700 °C for 9 hrs. All emission spectra showed a prominent band centered at 442 nm that was attributed to oxygen related defects in the CeO2-TiO2 nanocrystals. Two sharp absorption bands at 1418 cm-1 and 3323 cm-1 were attributed to the deformation and stretching vibration, and bending vibration of the OH group of water physisorbed to TiO2, respectively. The photocatalytic activities of Ce-TiO2 nanocrystals were investigated through the degradation of RhB under UV and UV+ visible light over a period of 8 hrs. After 8 hrs, the most intense absorption peak at 579 nm disappeared under the highest photocatalytic activity and 99.89% of RhB degraded under solar irradiation. Visible light-activated TiO2 could be prepared from metal-ion incorporation, reduction of TiO2, non-metal doping or sensitizing of TiO2 using dyes. Studying the antibacterial activity of Ce-TiO2 nanocrystals against E. coli revealed significant activity when 10 μg was used, suggesting that it can be used as an antibacterial agent. Its effectiveness is likely related to its strong oxidation activity and superhydrophilicity. This study also discusses the mechanism of heterogeneous photocatalysis in the presence of TiO2.

| S-EPMC5128916 | biostudies-literature

Co-assembled MoS2-TiO2 Inverse Opal Photocatalysts for Visible Light-Activated Pharmaceutical Photodegradation.

Project description:Heterostructured photocatalytic materials in the form of photonic crystals have been attracting attention for their unique light harvesting ability that can be ideally combined with judicious compositional modifications toward the development of visible light-activated (VLA) photonic catalysts, though practical environmental applications, such as the degradation of pharmaceutical emerging contaminants, have been rarely reported. Herein, heterostructured MoS2-TiO2 inverse opal films are introduced as highly active immobilized photocatalysts for the VLA degradation of tetracycline and ciprofloxacin broad-spectrum antibiotics as well as salicylic acid. A single-step co-assembly method was implemented for the challenging incorporation of MoS2 nanosheets into the nanocrystalline inverse opal walls. Compositional tuning and photonic band gap engineering of the MoS2-TiO2 photonic films showed that integration of low amounts of MoS2 nanosheets in the inverse opal framework maintains intact the periodic macropore structure and enhances the available surface area, resulting in efficient VLA antibiotic degradation far beyond the performance of benchmark TiO2 films. The combination of broadband MoS2 visible light absorption and photonic-assisted light trapping together with the enhanced charge separation that enables the generation of reactive oxygen species via firm interfacial coupling between MoS2 nanosheets and TiO2 nanoparticles is concluded as a competent approach for pharmaceutical abatement in water bodies.

| S-EPMC10515384 | biostudies-literature

Mesoporous Cu-Cu2O@TiO2 heterojunction photocatalysts derived from metal-organic frameworks.

Project description:This study reveals a unique Cu-Cu2O@TiO2 heterojunction photocatalyst obtained with metal-organic framework as the precursor, which can be utilized in dye photodegradation under visible light irradiation. The composition, structure, morphology, porosity, optical properties and photocatalytic performance of the obtained catalysts were all investigated in detail. The Cu-Cu2O@TiO2 nanocomposite is composed of lamellar Cu-Cu2O microspheres embedded by numerous TiO2 nanoparticles. Methylene blue, methyl orange and 4-nitrophenol were used as model pollutants to evaluate the photocatalytic activity of the Cu-Cu2O@TiO2 nanocomposite for dye degradation under visible light irradiation. Nearly 95% decolourisation efficiency of Methylene blue was achieved by the Cu-Cu2O@TiO2 photocatalyst within 3 h, which is much higher than that of TiO2 or Cu2O catalysts. The excellent photocatalytic activity was primarily attributed to the unique MOF-based mesoporous structure, the enlarged photo-adsorption range and the efficient separation of the charge carriers in the Cu-Cu2O@TiO2 heterojunction.

| S-EPMC9052089 | biostudies-literature

Adsorption and visible-light photodegradation of organic dyes with TiO2/conjugated microporous polymer composites.

Project description:A series of composite materials made of TiO2 and conjugated microporous polymers (CMPs) were prepared with a hydrothermal method and used as both adsorbents and photocatalysts for the adsorption and visible-light photodegradation of organic dyes in aqueous solutions. It is found that the blending of CMPs can significantly improve both the adsorption capacity and the photocatalytic degradation activity of TiO2 towards organic dyes.

| S-EPMC9086925 | biostudies-literature

Synergy of Au-Pt for Enhancing Ethylene Photodegradation Performance of Flower-like TiO2.

Project description:Efficient and low-cost degradation of ethylene has always been a difficult problem in the storage and transportation of fruits and vegetables. Although photocatalysis is considered to be a feasible and efficient solution for ethylene degradation, the low degradation ability of conventional catalysts for small non-polar molecules limits its application. TiO2 has the advantage of tunable microstructure, but it also has the defects of wide band gap and low utilization of sunlight. The surface plasmon resonance (SPR) effect of noble metals can effectively improve the visible light absorption range of catalysts, and the synergy of noble metals further enhances the photocatalytic ability. Herein, we developed a series of AuPt catalysts through the photo-deposition method. Benefited from the SPR effect and the synergy of Au and Pt, the efficiency of AuPt-TiO2 was 19.9, 4.64 and 2.42 times that of TiO2, Au-TiO2 and Pt-TiO2, and the photocatalytic degradation ability of AuPt-TiO2 was maintained in five cyclic stability tests. Meanwhile, the transient photocurrent spectra and PL spectra proved that the light absorption capacity and carrier separation efficiency of AuPt-TiO2 were enhanced. This work provides a new direction for enhancing non-polar small-molecule photodegradation of semiconductors.

| S-EPMC9505558 | biostudies-literature

Rhombohedral/Cubic In2O3 Phase Junction Hybridized with Polymeric Carbon Nitride for Photodegradation of Organic Pollutants.

Project description:In recent studies, phase junctions constructed as photocatalysts have been found to possess great prospects for organic degradation with visible light. In this study, we designed an elaborate rhombohedral corundum/cubic In2O3 phase junction (named MIO) combined with polymeric carbon nitride (PCN) via an in situ calcination method. The performance of the MIO/PCN composites was measured by photodegradation of Rhodamine B under LED light (λ = 420 nm) irradiation. The excellent performance of MIO/PCN could be attributed to the intimate interface contact between MIO and PCN, which provides a reliable charge transmission channel, thereby improving the separation efficiency of charge carriers. Photocatalytic degradation experiments with different quenchers were also executed. The results suggest that the superoxide anion radicals (O2-) and hydroxyl radicals (·OH) played the main roles in the reaction, as opposed to the other scavengers. Moreover, the stability of the MIO/PCN composites was particularly good in the four cycling photocatalytic reactions. This work illustrates that MOF-modified materials have great potential for solving environmental pollution without creating secondary pollution.

| S-EPMC9695553 | biostudies-literature

Visible-Light Driven Photodegradation of Industrial Pollutants Using Nitrogen-Tungsten Co-Doped Nanocrystalline TiO2: Spectroscopic Analysis of Degradation Reaction Path.

Project description:The purpose to conduct this research work is to study the effect of photocatalytic degradation by developing cost-effective and eco-friendly nitrogen and tungsten (metal/non-metal) co-doped titania (TiO2). The inherent characteristics of synthesized nanoparticles (NPs) were analyzed by Fourier transform infra-red spectroscopy (FT-IR), ultra-violet visible (UV-Vis) spectroscopy, Raman spectroscopy, Field emission scanning electron microscopy (FE-SEM), energy dispersive X-ray spectroscopy (EDX), dynamic light scattering (DLS), X-ray diffraction (XRD) spectrometry, and atomic force microscopy (AFM). Co-doping of metal and non-metal has intensified the photocatalysis trait of TiO2 nanoparticles in an aqueous medium. This co-doping of transition metal ions and modification of nitrogen extended the absorption into the visible region subsequently restraining the recombination of electrons/holes pair. The stronger light absorption in the visible region was required for the higher activity of photodegradation of dye under visible light illumination to confine bandgap energy which results in accelerating the rate of photodegradation. After efficient doping, the bandgap of titania reduced to 2.38 eV and caused the photodegradation of malachite green in visible light. The results of photocatalytic degradation were confirmed by using UV/Vis. spectroscopy and high-performance liquid chromatography coupled with a mass spectrophotometer (HPLC-ESI-MS) was used for the analysis of intermediates formed during photocatalytic utility of the work.

| S-EPMC9267965 | biostudies-literature

Intermixing of MoS2 and WS2 photocatalysts toward methylene blue photodegradation.

Project description:Visible-light-driven photocatalysis using layered materials has garnered increasing attention regarding the degradation of organic dyes. Herein, transition-metal dichalcogenides MoS2 and WS2 prepared by chemical vapor deposition as well as their intermixing are evaluated for photodegradation (PD) of methylene blue under solar simulator irradiation. Our findings revealed that WS2 exhibited the highest PD efficiency of 67.6% and achieved an impressive PD rate constant of 6.1 × 10-3 min-1. Conversely, MoS2 displayed a somewhat lower PD performance of 43.5% but demonstrated remarkable stability. The intriguing result of this study relies on the synergetic effect observed when both MoS2 and WS2 are combined in a ratio of 20% of MoS2 and 80% of WS2. This precise blend resulted in an optimized PD efficiency and exceptional stability reaching 97% upon several cycles. This finding underscores the advantageous outcomes of intermixing WS2 and MoS2, shedding light on the development of an efficient and enduring photocatalyst for visible-light-driven photodegradation of methylene blue.

| S-EPMC11228617 | biostudies-literature

Integrated Adsorption-Photodegradation of Organic Pollutants by Carbon Xerogel/Titania Composites.

Project description:Recent studies on the removal of pollutants via adsorption include the use of carbon-based adsorbents, due to their high porosity and large surface area; however, such materials lack photoactive properties. This study evaluates the synergistic effect of integrated mesoporous carbon xerogel (derived from resorcinol formaldehyde) and titanium dioxide (TiO2) for combined adsorption and photodegradation application. The complex formed between carbon xerogel and TiO2 phase was investigated through FTIR, proving the presence of a Ti-O-C chemical linkage. The physicochemical properties of the synthesised adsorbent-photocatalyst were probed using FESEM, BET analysis and UV-Vis analysis. The kinetics, equilibrium adsorption, effect of pH, and effect of adsorbent dosage were investigated. The expansion of the absorbance range to the visible range was verified, and the corresponding band gap evaluated. These properties enabled a visible light response when the system was exposed to visible light post adsorption. Hence, an assistive adsorption-photodegradation phenomenon was successfully executed. The adsorption performance exhibited 85% dye degradation which improved to 99% following photodegradation. Further experiments showed the reduction of microorganisms under visible light, where no microbial colonies were observed after treatment, indicating the potential application of these composite materials.

| S-EPMC9735923 | biostudies-literature

Improvement of photocatalytic activity in the degradation of 4-chlorophenol and phenol in aqueous medium using tin-modified TiO2 photocatalysts.

Project description:In this work, we present the synthesis of TiO2 photocatalysts modified with different % mol of tin using the sol-gel method. The materials were characterized using different analytical techniques. The Rietveld refinement, XPS, Raman and UV-Vis techniques confirm the substitution of tin in the TiO2 structural lattice due to changes in crystal lattice parameters, the low-energy shift of the Sn 3d5/2 orbital, generation of oxygen vacancies and the decreased band gap and increased BET surface area. The material with 1 mol% tin shows superior catalytic activity compared to the references for the degradation of 40 ppm 4-chlorophenol (3 hours of reaction) and 50 ppm phenol (6 hours of reaction). Reactions fit pseudo first order kinetics in both instances. The increase in photodegradation efficiency was attributed to the generation of energy levels below the TiO2 conduction band caused by the incorporation of 1% mol of tin, oxygen vacancies, and the heterojunction formed between the brookite-anatase-rutile, causing inhibition of the recombination of the electron (e-) and hole (h+) photogenerated species. The easy synthesis, low cost and increased photodegradation efficiency of the photocatalyst with 1 mol% tin have the potential to favor the remediation of recalcitrant compounds in water.

| S-EPMC10173256 | biostudies-literature