| Literature DB >> 36060494 |
Jayaseelan Arun1, S Nachiappan2, Goutham Rangarajan3, Ram Prasath Alagappan4, K P Gopinath5, Eric Lichtfouse6.
Abstract
Global pollution is calling for advanced methods to remove contaminants from water and wastewater, such as TiO2-assisted photocatalysis. The environmental applications of titanium dioxide have started after the initial TiO2 application for water splitting by Fujishima and Honda in 1972. TiO2 is now used for self-cleaning surfaces, air and water purification systems, microbial inactivation and selective organic conversion. The synthesis of titanium dioxide nanomaterials with high photocatalytic activity is actually a major challenge. Here we review titanium dioxide photocatalysis with focus on mechanims, synthesis, and applications. Synthetic methods include sol-gel, sonochemical, microwave, oxidation, deposition, hydro/solvothermal, and biological techniques. Applications comprise the production of energy, petroleum recovery, and the removal of microplastics, pharmaceuticals, metals, dyes, pesticides, and of viruses such as the severe acute respiratory syndrome coronavirus 2.Entities:
Keywords: Emerging pollutant; Photocatalysis; Photocatalyst; Titanium dioxide; Wastewater
Year: 2022 PMID: 36060494 PMCID: PMC9419126 DOI: 10.1007/s10311-022-01503-z
Source DB: PubMed Journal: Environ Chem Lett ISSN: 1610-3653 Impact factor: 13.615
Fig. 1Comparison of energy band gap levels of undoped (pure) and doped titanium dioxide. Upon irradiation with light of suitable energy that corresponds to the bandgap, the electrons present in the valence band of titanium dioxide get excited and their concurrent transfer to the conduction band occurs. This phenomenon facilitates the generation of various reactive oxygen species leading to the degradation of pollutants present in the wastewater. H2O: water, O2: oxygen, Eg: energy gap, h: photon energy
Synthetic methods for titanium dioxide-based catalysts for environmental applications. TiO2: Titanium dioxide, Hg: mercury, CuO: copper oxide, NO: nitrous oxide, HCHO: formaldehyde, SO2: sulphur dioxide, BTEX: benzene, toluene, ethylbenzene, xylene
| Catalyst | Synthesis method | Intended application | Category of application | Initial concentration | Illumination condition | Optimal performance | References |
|---|---|---|---|---|---|---|---|
| TiO2 films | Sol–gel | Trichloroethylene degradation | Air pollution mitigation | 50 ppm | Ultraviolet lamp | Up to 90% conversion | Arconada et al. ( |
| TiO2-P25 | Commercial P25 | Nitrous oxide removal | Air pollution mitigation | 5 ppm | Ultraviolet lamp (25 W) | 70% conversion | Devahasdin et al. ( |
| TiO2-P25 | Commercial P25 | HCHO:SO2:BTEX | Air pollution mitigation | 1:1:1 ratio of gases at 1, 10 and 50 ppm | 6 W Ultraviolet lamp | 88% conversion | Ao et al. ( |
| TiO2-aluminium silicate | Sol–gel | SO2:NO:Hg0 | Air pollution mitigation | 400–1200 ppm SO2, 50–300 ppm NO, 50 µg/m3 Hg0 | 9 W Ultraviolet lamp | Up to 80% | Yuan et al. ( |
| TiO2nanofibre | Electrospinning | SO2 | Air pollution mitigation | 100–300 ppm in air | 300 W Xenon arc lamp | Up to 100% | Wang et al. ( |
| TiO2 | Precursor hydrolysis | Arsenic removal | Water treatment–adsorption | Arsenic = 26.7 µm | – | 90% | Pena et al. ( |
| TiO2 | Precursor hydrolysis | Arsenic removal | Water treatment–adsorption | Arsenic = 0–80 ppm | – | 85% | Xu and Meng ( |
| TiO2 | Commercial P25 | Methylene blue removal | Water treatment–adsorption | Methylene blue = 56.5 ppm | – | 88.5% | Munjal et al. ( |
| TiO2/chitosan | Commercial TiO2 | Dye (thymol violet) removal and antimicrobial activity | Water treatment– adsorption | Thymol violet = 120 ppm | – | 88% | Kamal et al. ( |
| TiO2 nanotube | Anodization | Bacteria ( | Water treatment–microbial decontamination | 106 cpu/mL | Ultraviolet lamp | 95% disinfection | Ng et al. ( |
| TiO2 | Commercial P25 | Fungi ( | Water treatment–microbial decontamination | 103 cpu/mL | Sunlight | 99.99% removal | Fernández-Ibáñez et al. ( |
| TiO2 | Commercial P25 | Protozoa ( | Water treatment–microbial decontamination | 15 × 106 oocytes | 1100 W Xenon arc lamp | 99.33% | Abeledo-Lameiro et al. ( |
| Bismuth/TiO2 | Sol–gel | Water splitting/methanol sacrificial agent | Sustainable energy | – | Ultraviolet lamp | 3.5 mL hydrogen production | Wu et al. ( |
| Platinum/Nitrogen/TiO2 | Hydrothermal | Water splitting/glycerol sacrificial agent | Sustainable energy | – | 250 W Ultraviolet lamp | 3200 µmol hydrogen production | Slamet et al. ( |
| Platinum/TiO2−xNx | Microemulsification | Water splitting/methanol sacrificial agent | Sustainable energy | – | 400 W halogen lamp | 130 µmol hydrogen production | Lin et al. ( |
| Nickel/TiO2 | Precipitation | Water splitting/methanol sacrificial agent | Sustainable energy | – | 3 W Ultraviolet light emitting diode | 3056 μmol h−1 g−1 | Yu et al. ( |
| Silver/TiO2 | Sol–gel synthesis | Carbon dioxide reduction/water sacrificial agent | Pollution mitigation/sustainable energy | – | Ultraviolet light | Methane = 10.5 Methanol = 2 μmol/gcatalyst | Krejčíková et al. ( |
| TiO2 | Wet impregnation | Carbon dioxide reduction/water sacrificial agent | Pollution mitigation/sustainable energy | – | 300 W Xenon arc lamp | Methane = 52 μmol/gcatalyst | Meng et al. ( |
| Palladium/TiO2 | Thermal hydrolysis | Carbon dioxide reduction/water sacrificial agent | Pollution mitigation/sustainable energy | – | 500 W Hg lamp | Methane = 1.415 CO = 0.722 μmol/g.h | Camarillo et al. ( |
| CuO/TiO2 | Sol–gel and wet impregnation | Carbon dioxide reduction/water sacrificial agent | Pollution mitigation/sustainable energy | – | 6 W Hg lamp | Methanol = 4120 μmol/g | Thamaraiselvi and Sivakumar ( |
Fig. 2Methodologies of the sol–gel process for the synthesis of titanium dioxide materials. Gelling, spinning, precipitation and coating are the most common techniques used in the sol–gel process. Dense ceramic material (xerogel) and aerogels are produced from the gelling process. Fibres, uniform powder and dense film (xerofilm) are produced from the other three methods
Fig. 3Cathodic electrophoretic deposition cell (Srikanth et al. 2017). The photocatalyst is suspended in the solvent phase with a steady direct voltage (25–400 V). Electrolysis produces ions, which migrate towards the oppositely charged electrode as a result of electrophoresis and gets deposited over the electrode support
Fig. 4Spray pyrolysis. The spray gun provides the point for the substrate that was placed in the hot plate to get in contact with the precursor solution. Licensed from Elsevier books “Nanosensors for smart cities”, Han et al. (2020)
Physical, chemical and biological methods for the synthesis of titanium dioxide nanoparticles
| Method | Major factors | Advantage(s) | Disadvantage(s) | References | |
|---|---|---|---|---|---|
| Physical and Chemical method | Sol–gel | pH, time, temperature, agitation, nature of solvent and catalyst | Low operation temperature (< 100 °C), cheap and high yield | Slow process, difficult to synthesize monoliths, high precursors cost | Esposito ( |
| Sonochemical-assisted technique | Intensity of acoustic frequency, temperature, static pressure | Fast reaction rate, production of ultra-fine particles and no chemical addition | Low yield, high energy demand | Savun-Hekimouglu ( | |
| Microwave-assisted technique | Frequency and wavelength of microwave, temperature | Selective heating, short reaction time, easy handling and high yield | Expensive process, unfeasible to monitor reaction, difficult to scale up | Mikrovalov ( | |
| Oxidation techniques (anodization) | Electrolyte type and concentration, batch temperature, voltage, pH | Easy to scale up, time-efficient, facile, effective in synthesis of high quality 1D nanostructures | Limited mass production, employed mostly for nanotubes growth | Kaur et al. ( | |
| Electrophoretic deposition | Electrolyte type and nature, temperature, voltage | Simple, low cost equipment, high reproducibility, short product formation time | Requires high sintering temperatures, difficult to achieve fissure less coating, only films can be made | Chava et al. ( | |
| Spray Pyrolysis | Nature of precursor solution, pressure, properties of the instrument | Cost effective, do not require high quality reagents, morphology of product is easy to control | Hard to scale up, difficulties associated with determining growth temperature, oxidation of reagent when operated in air atmosphere | Gavrilović et al. ( | |
| Hydrothermal technique | Viscosity, heat capacity, thermal conductivity, dielectric constant, ionic product density | Easy handling, simple, production of high quality 1D nanostructures | Slow process, inability to monitor crystal growth, high equipment cost | Liu et al. ( | |
| Solvothermal technique | Viscosity, heat capacity, thermal conductivity, dielectric constant, ionic product density | Simple equipment, uniform production on larger area | Requirement of pure organic solvents, high pressure and temperatures are needed | Wang et al. ( | |
| Biological method | Concentration, temperature, pH | Eco friendly, devoid of using any toxic chemicals, cheap and safe | Cell growth of organisms determine size of nano particles, low yield | Wu et al. ( | |
Applications of titanium dioxide based substrates on simultaneous removal of heavy metals and dyes. TiO2: Titanium dioxide, SiO2: silicon dioxide
| TiO2-based substrate | Pollutants considered | Removal efficiency | References |
|---|---|---|---|
| Polyvinyl alcohol and acrylamide incorporated on TiO2/SiO2 nanopowders | Basic blue 3 dye and copper (II) ions | Basic blue 3 dye = 93.5 and copper (II) = 95.2% after 7 h and 6 h, respectively | Elbarbary and Gad ( |
| Natural melamine/TiO2 hybrid | Methyl orange dye and chromium (IV) | Around 90% reduction on dye and 100% on chromium (IV), after 3 h of visible light irradiation | Xie et al. ( |
| TiO2/3-cyanopropyltriethoxysilane/metformin polyether sulfone nanocomposite membrane | Copper (II) ions and dye removal from liquorice extraction plant (LEP) wastewater | 90.1% removal of copper ions after 60 min and 88% chemical oxygen demand removal on LEP wastewater after 150 min | Barahimi et al. ( |
| Bismuth molybdenum oxide type-II loaded on TiO2 nanotubes | Methyl orange, rhodamine blue, methylene blue and chromium (VI) | Removal of nearly 100%, 75%, 100% and 100% for methyl orange, rhodamine blue, methylene blue and chromium (VI)ions, respectively, after 120 min of simulative sunlight irradiation | Liu et al. ( |
| TiO2/SiO2 doped with iron | Basic red 29, basic blue 41, basic yellow 51 and chromium (VI) | Reduction in total organic carbon = 74.39% and 78.04% under visible and solar light, respectively | Ghanbari et al. ( |
| Electro-spinning carbon nanofibers/TiO2 using polyacrylonitrile base | Methylene blue dye and different metal ions such as lead, copper and cadmium ions | A maximum rejection rate of 84%, 87%,73% and 66% for methylene blue, lead, copper and cadmium, respectively, after 1500 min | Kumar et al. ( |
Fig. 5Mechanism of dye degradation by titanium dioxide. Upon light induction the excitation of electrons occurs from valence band to conduction band. This triggers the formation of hydroxyls ions. Oxygen compounds also get converted into hydroxyl groups via hydrogen peroxide formation. This hydroxyl groups further help in formation of reduced and oxidized compounds upon dye degradation
Titanium dioxide-based Janus micromotors propelled by different propellants for the removal of microplastics
| Substrate | Conditions | Results | Reference |
|---|---|---|---|
| Titanium dioxide/water-soluble conjugated polyelectrolyte/glucose oxidase | Visible light; hydrogen peroxide produced through the decomposition of glucose using glucose oxidase | Maximum velocity of 7.49 μm S−1 observed under visible light | Noh et al. ( |
| Hedgehog-shaped titanium dioxide/functional multiwall carbon nanotubes | Ultraviolet light illumination | Velocity of 8.9 μm S−1 is achieved under 160 mW cm−2 ultraviolet light illumination | Jiang et al. ( |
| Titanium dioxide/gold nanowire-based motor | Ultraviolet irradiation | A velocity of 5.6 ± 1.5 μm S−1 is achieved in deionized water while it was 2.41 ± 0.53 µm S−1 and 2.27 ± 0.35 µm S−1, respectively at pH = 4 and 10 | Chen et al. ( |
| Titanium dioxide/manganese dioxide | Hydrogen peroxide decomposed to oxygen bubbles, which propels the micromotor acts as fuel | Maximum speed of 48.1 μm S−1 at [hydrogen peroxide] = 30% with maximum instantaneous velocity of 135 μm S−1 | Ge et al. ( |
Titanium dioxide-based substrates for electrocatalysis for energy. Nb-MoS2: niobium-molybdenum disulfide, TiO2: titanium dioxide, Ti3C2Tx: titanium carbide, Co3O4: cobalt oxide, Ag3PO4: Tri-silver phosphate, Bi2WO6: bismuth tungstate
| Catalyst | Overpotential and other remarks | References |
|---|---|---|
| Cobalt, Nb-MoS2 nanosheets shelled in micro-TiO2 hollow spheres | • Hydrogen evolution reaction = 58.8 mV and oxygen evolution reaction = 260.0 mV to deliver current density of 10 mA cm−2 • Catalyst needed an operating voltage of 1.57 V to achieve this current density | Nguyen et al. ( |
| Ag3PO4-Bi2WO6-TiO2 | • Oxygen evolution reaction = 360 mV, this nanohybrid was stable and exhibited a remarkable efficiency of 99.8% for the oxygen evolution reaction • Highly efficient in comparison with individual components from where it was derived | Mandari et al. ( |
| TiO2/Co3O4 composite | • Oxygen evolution reaction = 270 mV (at 10 mA cm−2), with a Tafel slope of 60 mV dec−1 and found that overpotential decreases with an increase in titania content in the composite • This composite is highly stable for 45 h | Aftab et al. ( |
| Ti3C2Tx (MXene) decorated by phosphorus-doped TiO2 (P–TiO2@Ti3C2) | • Less overpotential of 97 mV (at 10 mA cm−2) and a low Tafel slope of 48.4 mV dec−1, which performed more efficient than that in darkness • The catalyst was found to be more stable for more than 50 h under light irradiation and alkaline conditions. Outperformed than Mxene and corresponding derived materials | Deng et al. ( |
| Palladium@TiO2–(hollow) core–shell | • This novel catalyst (with a trace of Pd—0.05 wt%) required the lowest overpotential of 0.43 V at 10 mA cm−2 with a Tafel slope of 63 mV dec−1 • Outperformed that of the commercial TiO2 (0.92 V, 636 mV dec−1) | Shu et al. ( |
Methodologies to remove SAR-CoV-2 using titanium dioxide-based substrates. TiO2: titanium dioxide, Al2O3: Aluminium oxide IC50: inhibitory concentration, CC50: cytotoxic concentration, SARS: severe acute respiratory syndrome, CoV: coronavirus
| Target organism | Materials employed | Methodology | Results | References |
|---|---|---|---|---|
| SARS-CoV-2 spike protein | TiO2 and Al2O3 | Adsorption | Adsorption on TiO2 proceeds about one order of magnitude faster than that of Al2O3 | Xin et al. ( |
SARS-CoV-2: (1) Spike pseudo-typed virions (2) fully infectious virus | TiO2 and TiO2-silver coated on wall tiles | Free radical attack on viruses | Spike viral load was decreased by four orders of magnitude after 1 h, while no active virus was found after 5 h, no significant difference was observed between TiO2 and TiO2-silver | Micochova et al. ( |
| SARS-CoV-2 pseudo-virus | TiO2 supported silver—single atom nano enzyme (silver-TiO2 SAN) | Adsorption and then reactive oxygen species attack | Silver-TiO2 SAN produced maximum adsorption (99.65%) than nano-TiO2, silver | Wang et al. ( |
| A broad range of pathogens including SAR-CoV-2, Hepatitis C | Nanosized TiO2 | Hydroxyl attack on viral Ribo nucleic acid genome | At low irradiation, TiO2 inhibited SAR-CoV-2, Hepatitis C and other pathogens | Tong et al. ( |
| SAR-CoV-2 cells | TiO2 nanoparticles and nanotubes | Reactive oxygen species and titanium radicals damaged proteins, Deoxy Ribonucleic acids and lipid | TiO2-nanoparticles and nanotubes have potent antiviral activity at very low concentration (IC50 = 568.6 ng/mL), with a weak cytotoxic effect on the cellular host (CC50 = 399.1 ng/mL), where CC50and IC50 denotes cytotoxic half concentration and half maximal inhibitory concentration, respectively | Hamza et al. ( |
Advanced titanium dioxide-based substrates for the removal of pharmaceutical and personal care products. PPCPs: pharmaceutical and personal care products, C3N4: carbon nitride, TiO2: titanium dioxide, Fe3O4: iron oxide, SiO2: silicon dioxide, BiOCl: bismuth oxychloride
| TiO2 based substrate | Target Pollutant | Results | References |
|---|---|---|---|
| 2,5-Bis (tributylstannyl) thiophene-perylene diimide-T@TiO2 (Bis-PDI-T@TiO2) composite | Carbamazepine (CBZ) (a typical PPCP) | Complete degradation of CBZ (dosage: 5 ppm) achieved after 30 min under visible light, in presence of persulfate | Yang et al. ( |
| Copper oxide/TiO2 nanoparticle coated ceramic ultrafiltration membrane | Phthalates and parabens from synthetic systems (10–1000 ppb concentration) | More than 99% removal achieved | Bhattacharya et al. ( |
| Ultra-thin, defect rich copper-doped TiO2nanosheets with rich oxygen vacancies | Tetracycline and acetaminophen | Nearly 100% removal was achieved with both the pollutants using photocatalyst containing 4% copper, after 100 min of visible light irradiation | Qu et al. ( |
| BiOCl; TiO2 | Atenolol and ibuprofen | BiOCl degraded ibuprofen 15 times faster than TiO2 while TiO2 degraded atenolol 2.2 times faster than BiOCl, under ultraviolet irradiation (254 nm) | Speller ( |
| Ternary film of Fe2O3–TiO2 Polyvinyl pyrrolidine coated on a glass tube | Triclosan | 83.27% of degradation efficiency was observed at optimum conditions under solar irradiation | Pragada and Thalla ( |
| Terephthalic acid-functionalized g–C3N4/TiO2/Fe3O4@SiO2 heterojunction nano-photocatalyst | Ibuprofen, benzophenone-3, carbamazepine in Real sewage effluent | Ibuprofen after 120 min = 97%, benzophenone – 3 after 150 min = 94%, carbamazepine after 240 min = 94%; under visible light irradiation | Kumar et al. ( |
Degradation of pesticides using titanium dioxide-based substrates. Fe3O4: ferric oxide, TiO2: titanium dioxide, LaFeO3: lanthanum iron oxide
| Pollutant | Substrate | Results | References |
|---|---|---|---|
| Atrazine and dimethoate residues in three samples as deionized water, wastewater and agricultural wastewater containing these residues | TiO2 in the presence of ultraviolet irradiation of (1) 254 nm and (2) 306 nm | Complete degradation is achieved after 12 h under 306 nm ultraviolet irradiation; dimethoate degrades more easily than atrazine | EL-Saeid et al. ( |
| Monocrotophos (dimethyl (E)-1-methyl-2-(methyl carbamoyl)vinyl phosphate) | MIL-88(IRON) anchored TiO2-chitosan(2 dimensional) hybrid nanocomposite | 98.79% degradation observed at optimized conditions (within 30 min) under visible light irradiation | Vigneshwaran et al. ( |
| Atenolol removal from domestic wastewater effluent | Iron doped with TiO2 nanoparticles, synthesized using | A maximum of 85% of atenolol was degraded under visible light for 105 min at pH = 9 | Bhuvaneswari et al. ( |
| Herbicide 2,4-dichlorophenoxyacetic acid (2,4D), and the insecticide imidacloprid (1-(6-chloro-3-pyridinylmethyl)-Nnitro-2-imidazolidinimine) (IM) | Molecularly imprinted (MI) TiO2 powder with pesticides (TiO2 MI/2,4-D; TiO2 MI/IM) | At 368 nm ultraviolet irradiation, TiO2 MI/2,4-D produced 6 times faster degradation of 2,4-D in comparison with bare TiO2, while TiO2 IM/IM produced 2 times faster degradation of IM in comparison with bare TiO2 | Fiorenza et al. ( |
| Fungicide myclobutanil (C15H17ClN4) | LaFeO3@TiO2 heterojunction photocatalysts | • Complete removal achieved after 180 min under solar light • 85% removal was observed after 240 min using each pure substrate, viz. LaFeO3 and TiO2 | Garcia-Muñoz et al. ( |
| Zoxamide [3, 5-dichloro-N-(3-chloro, 1-ethyl, 1-methyl, 2-oxopropyl)-4 methyl benzamide] | Titanium dioxide nanoparticles (TiO2nanoparticles) Synthesized using aqueous leaf extract of | • The lowest concentration (105 mg/L) of zoxamide exhibits the highest degradation rate (0.32048 h−1) • Degradation follows pseudo-first-order kinetics under ultraviolet irradiation | Purkait et al. ( |
| Atrazine degradation | Magnetic Fe3O4-TiO2/graphene oxides nanocomposite | • This nano-enzyme has a dual role, as highly selective in detecting and degrading atrazine • Within 40 min, 100% degradation was achieved in acidic conditions (pH = 3) under sunlight | Boruah and Das ( |