Displaying publications 81 - 100 of 384 in total

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  1. Stability evaluation and formula optimization of cellulose-based scaffold for the air-liquid interface cultivation of Navicula incerta
    Yap JX, Leo CP, Mohd Yasin NH, Show PL, Derek CJC
    Environ Res, 2021 08;199:111298.
    PMID: 33971133 DOI: 10.1016/j.envres.2021.111298
    Culture scaffolds allow microalgae cultivation with minimum water requirement using the air-liquid interface approach. However, the stability of cellulose-based scaffolds in microalgae cultivation remains questionable. In this study, the stability of regenerated cellulose culture scaffolds was enhanced by adjusting TiO2 loading and casting gap. The membrane scaffolds were synthesized using cellulose dissolved in NaOH/urea aqueous solution with various loading of TiO2 nanoparticles. The TiO2 nanoparticles were embedded into the porous membrane scaffolds as proven by Fourier transform infrared spectra, scanning electron microscopic images, and energy-dispersive X-ray spectra. Although surface hydrophilicity and porosity were enhanced by increasing TiO2 and casting gap, the scaffold pore size was reduced. Cellulose membrane scaffold with 0.05 wt% of TiO2 concentration and thickness of 100 μm attained the highest percentage of Navicula incerta growth rate, up to 37.4%. The membrane scaffolds remained stable in terms of weight, porosity and pore size even they were immersed in acidic solution, hydrogen peroxide or autoclaved at 121 °C for 15 min. The optimal cellulose membrane scaffold is with TiO2 loading of 0.5 wt% and thickness of 100 μm, resulting in supporting the highest N. incerta growth rate and and exhibits good membrane stability.
    Matched MeSH terms: Titanium
  2. Fulltext SrCo1-xTixO3-δ perovskites as excellent catalysts for fast degradation of water contaminants in neutral and alkaline solutions
    Miao J, Sunarso J, Su C, Zhou W, Wang S, Shao Z
    Sci Rep, 2017 03 10;7:44215.
    PMID: 28281656 DOI: 10.1038/srep44215
    Perovskite-like oxides SrCo1-xTixO3-δ (SCTx, x = 0.1, 0.2, 0.4, 0.6) were used as heterogeneous catalysts to activate peroxymonosulfate (PMS) for phenol degradation under a wide pH range, exhibiting more rapid phenol oxidation than Co3O4 and TiO2. The SCT0.4/PMS system produced a high activity at increased initial pH, achieving optimized performance at pH ≥ 7 in terms of total organic carbon removal, the minimum Co leaching and good catalytic stability. Kinetic studies showed that the phenol oxidation kinetics on SCT0.4/PMS system followed the pseudo-zero order kinetics and the rate on SCT0.4/PMS system decreased with increasing initial phenol concentration, decreased PMS amount, catalyst loading and solution temperature. Quenching tests using ethanol and tert-butyl alcohol demonstrated sulfate and hydroxyl radicals for phenol oxidation. This investigation suggested promising heterogeneous catalysts for organic oxidation with PMS, showing a breakthrough in the barriers of metal leaching, acidic pH, and low efficiency of heterogeneous catalysis.
    Matched MeSH terms: Titanium
  3. Fulltext Spin-polarized Second Harmonic Generation from the Antiferromagnetic CaCoSO Single Crystal
    Reshak AH
    Sci Rep, 2017 04 13;7:46415.
    PMID: 28406164 DOI: 10.1038/srep46415
    The spin-polarized second harmonic generation (SHG) of the recently synthesized CaCoSO single crystal is performed based on the calculated electronic band structure. The calculation reveals that the spin-up (↑) channel of CaCoSO possesses a direct energy gap (Γv-Γc) of about 2.187 eV, 1.187 eV (Kv-Kc) for the spin-down (↓) channel and an indirect gap (Γv-Kc) of about 0.4 eV for the spin-polarized CaCoSO single crystal. The linear optical properties obtained reveal that the recently synthesized crystal exhibits considerable anisotropy with negative uniaxial anisotropy and birefringence favor to enhance the SHG. We have calculated the three non-zero tensor components of the SHG and found the is the dominat component, one with a large SHG of about (d33 = 6.936 pm/V at λ = 1064 nm), the half value of KTiOPO4 (KTP). As the values of (↑)  (↓) 1.187 eV> spin-polarized gap 0.4 eV; therefore, a smaller energy gap gives better SHG performance. Furthermore, the microscopic first hyperpolarizability, βijk, is calculated.
    Matched MeSH terms: Titanium
  4. Solution Processed Bi-Based Sensitized Solar Cell: Effects of Post Heat Treatment
    Chai YC, Jun HK
    J Nanosci Nanotechnol, 2019 Jun 01;19(6):3505-3510.
    PMID: 30744778 DOI: 10.1166/jnn.2019.16099
    Nanosize semiconductors have been used as active sensitizers for the application of quantum dot-sensitized solar cells (QDSSC). "Green" sensitizers are introduced as an alternative for the toxic Cd and Pb based compounds. In this work, Bi₂S₃ quantum dots (QDs) were fabricated and used as sensitizers in QDSSC. QDs were grown on TiO₂ electrode via solution dipping process. Although the performance of "green" QDSSC is not as high as that of CdS or CdSe based QDSSCs, its performance can be enhanced with post heat treatment. The effect is dependent on the heat treatment temperature profile where gradual increase of sintering temperature is preferred. The effects of post heat treatment on Bi₂S₃ sensitized TiO₂ electrodes are investigated and discussed.
    Matched MeSH terms: Titanium
  5. Solar photolysis versus TiO2-mediated solar photocatalysis: a kinetic study of the degradation of naproxen and diclofenac in various water matrices
    Kanakaraju D, Motti CA, Glass BD, Oelgemöller M
    Environ Sci Pollut Res Int, 2016 Sep;23(17):17437-48.
    PMID: 27230148 DOI: 10.1007/s11356-016-6906-8
    Given that drugs and their degradation products are likely to occur as concoctions in wastewater, the degradation of a mixture of two nonsteroidal anti-inflammatory drugs (NSAIDs), diclofenac (DCF) and naproxen (NPX), was investigated by solar photolysis and titanium dioxide (TiO2)-mediated solar photocatalysis using an immersion-well photoreactor. An equimolar ratio (1:1) of both NSAIDs in distilled water, drinking water, and river water was subjected to solar degradation. Solar photolysis of the DCF and NPX mixture was competitive particularly in drinking water and river water, as both drugs have the ability to undergo photolysis. However, the addition of TiO2 in the mixture significantly enhanced the degradation rate of both APIs compared to solar photolysis alone. Mineralization, as measured by chemical oxygen demand (COD), was incomplete under all conditions investigated. TiO2-mediated solar photocatalytic degradation of DCF and NPX mixtures produced 15 identifiable degradants corresponding to degradation of the individual NSAIDs, while two degradation products with much higher molecular weight than the parent NSAIDs were identified by liquid chromatography mass spectrometry (LC-MS) and Fourier transform-ion cyclotron resonance-mass spectrometry (FT-ICR-MS). This study showed that the solar light intensity and the water matrix appear to be the main factors influencing the overall performance of the solar photolysis and TiO2-mediated solar photocatalysis for degradation of DCF and NPX mixtures.
    Matched MeSH terms: Titanium/chemistry*
  6. Solar photocatalytic degradation of mono azo methyl orange and diazo reactive green 19 in single and binary dye solutions: adsorbability vs photodegradation rate
    Ong SA, Min OM, Ho LN, Wong YS
    Environ Sci Pollut Res Int, 2013 May;20(5):3405-13.
    PMID: 23114839 DOI: 10.1007/s11356-012-1286-1
    The objective of this study was to examine the effects of adsorbability and number of sulfonate group on solar photocatalytic degradation of mono azo methyl orange (MO) and diazo Reactive Green 19 (RG19) in single and binary dye solutions. The adsorption capacity of MO and RG19 onto the TiO₂ was 16.9 and 26.8 mg/g, respectively, in single dye solution, and reduced to 5.0 and 23.1 mg/g, respectively, in the binary dye solution. The data obtained for photocatalytic degradation of MO and RG19 in single and binary dye solution were well fitted with the Langmuir-Hinshelwood kinetic model. The pseudo-first-order rate constants of diazo RG19 were significant higher than the mono azo MO either in single or binary dye solutions. The higher number of sulfonate group in RG19 contributed to better adsorption capacity onto the surface of TiO₂ than MO indicating greater photocatalytic degradation rate.
    Matched MeSH terms: Titanium/chemistry
  7. Single-step fabrication of highly stable amorphous TiO2 nanotubes arrays (am-TNTA) for stimulating gas-phase photoreduction of CO2 to methane
    Santos JS, Fereidooni M, Marquez V, Arumugam M, Tahir M, Praserthdam S, et al.
    Chemosphere, 2022 Feb;289:133170.
    PMID: 34875298 DOI: 10.1016/j.chemosphere.2021.133170
    This study investigates the facile fabrication of interfacial defects assisted amorphous TiO2 nanotubes arrays (am-TNTA) for promoting gas-phase CO2 photoreduction to methane. The am-TNTA catalyst was fabricated via a one-step synthesis, without heat treatment, by anodization of Titanium in Ethylene glycol-based electrolyte in a shorter anodizing time. The samples presented a TiO2 nanostructured array with a nanotubular diameter of 100 ± 10 nm, a wall thickness of 26 ± 5 nm, and length of 3.7 ± 0.3 μm, resulting in a specific surface of 0.75 m2 g. The am-TNTA presented prolonged chemical stability, a high exposed surface area, and a large number of surface traps that can reduce the recombination of the charge carriers. The am-TNTA showed promising photoactivity when tested in the CO2 reduction reaction with water under UV irradiation with a methane production rate of 14.0 μmol gcat-1 h-1 for a pure TiO2 material without any modification procedure. This enhanced photocatalytic activity can be explained in terms of surface defects of the amorphous structure, mainly OH groups that can act as electron traps for increasing the electron lifetime. The CO2 interacts directly with those traps, forming carbonate species, which favors the catalytic conversion to methane. The am-TNTA also exhibited a high stability during six reaction cycles. The photocatalytic activity, the significantly reduced time for synthesis, and high stability for continuous CH4 production make this nanomaterial a potential candidate for a sustainable CO2 reduction process and can be employed for other energy applications.
    Matched MeSH terms: Titanium
  8. Sifat kinetik dan isoterma penjerapan formaldehid ke atas komposit serbuk serat kelapa sawit-TiO2
    Nor Rahafza Abdul Manap, Roslinda Shamsudin, Mohd Norhafsam MaghpoR, Muhammad Azmi Abdul Hamid, Azman Jalar
    Sains Malaysiana, 2017;46:953-965.
    Sifat isoterma dan kinetik penjerapan formaldehid ke atas komposit serbuk serat kelapa sawit-TiO2 yang melibatkan sistem gas-pepejal adalah dikaji. Komposit serbuk serat kelapa sawit-TiO2 dihasilkan dengan mencampurkan serbuk kelapa sawit dan serbuk TiO2 dengan nisbah 8:2 menggunakan teknik pengisaran mekanik. Pengujian dijalankan di dalam kebuk ujian dengan komposit serbuk kelapa sawit-TiO2 dibiarkan untuk menjerap dan mengurangkan nilai kepekatan formaldehid secara pasif. Didapati nilai penjerapan maksima dan sifat kinetik penjerapan bergantung kepada kepekatan awal formaldehid. Kepekatan awal, Ci, 2.1 ppm dan 0.5 ppm masing-masing diwakili oleh pseudo-tertib pertama dan pseudo tertib kedua, manakala Ci = 0.75 dan 0.9 ppm diwakili oleh model Elovich. Isoterma penjerapan formaldehid diwakili oleh isoterma Freundlich dengan nilai korelasi tertinggi R2 = 0.9397 berbanding nilai korelasi isoterma Langmuir (R2 = 0.8692) dan isoterma Temkin (R2 = 0.8756). Parameter keseimbangan, 0
    Matched MeSH terms: Titanium
  9. Fulltext Shaping Ability of 2Shape and WaveOne Gold Files Using Cone-Beam Computed Tomography
    Singh S, Mirdha N, Shilpa PH, Tiwari RVC, Abdul MSM, Sainudeen S
    J Int Soc Prev Community Dent, 2019 06 07;9(3):245-249.
    PMID: 31198696 DOI: 10.4103/jispcd.JISPCD_411_18
    Aim and Objective: The aim of this study is to evaluate the apical transportation, centering ability, and volume of removed dentin of WaveOne Gold (WOG) and 2Shape with the use of cone-beam computed tomography.

    Materials and Methods: Freshly extracted mandibular teeth with sample size of thirty were carefully chosen and instrumented using the 2Shape and WOG rotary files. Preoperative and postinstrumentation cone-beam computed tomographic scans were done to accomplish mesial and distal dentin walls' measurements and volume of removed dentin calculations, apical transportation, and centering ratio. Statistical analysis was performed and confirmed by independent t-test. Statistical significance was set at 5%.

    Results: When shaping ability of 2Shape and WOG was evaluated, it was reported that there was no statistically significant differences noted among the groups in relation to the total volume of removed dentin, apical transportation, and centering ratio.

    Conclusion: It can be concluded that 2Shape and WOG preserved the original canal anatomy well and did not eliminate excess dentin during shaping and cleaning. Rotary nickel-titanium files which work on the principle of rotary movement attained an outcome analogous to that of the rotary files working on reciprocating motion in relation to alteration in angle.

    Matched MeSH terms: Titanium
  10. Self-assembly of a robust hydrogen-bonded octylphosphonate network on cesium lead bromide perovskite nanocrystals for light-emitting diodes
    Brown AAM, Hooper TJN, Veldhuis SA, Chin XY, Bruno A, Vashishtha P, et al.
    Nanoscale, 2019 Jul 07;11(25):12370-12380.
    PMID: 31215940 DOI: 10.1039/c9nr02566a
    We report the self-assembly of an extensive inter-ligand hydrogen-bonding network of octylphosphonates on the surface of cesium lead bromide nanocrystals (CsPbBr3 NCs). The post-synthetic addition of octylphosphonic acid to oleic acid/oleylamine-capped CsPbBr3 NCs promoted the attachment of octylphosphonate to the NC surface, while the remaining oleylammonium ligands maintained the high dispersability of the NCs in non-polar solvent. Through powerful 2D solid-state 31P-1H NMR, we demonstrated that an ethyl acetate/acetonitrile purification regime was crucial for initiating the self-assembly of extensive octylphosphonate chains. Octylphosphonate ligands were found to preferentially bind in a monodentate mode through P-O-, leaving polar P[double bond, length as m-dash]O and P-OH groups free to form inter-ligand hydrogen bonds. The octylphosphonate ligand network strongly passivated the nanocrystal surface, yielding a fully-purified CsPbBr3 NC ink with PLQY of 62%, over 3 times higher than untreated NCs. We translated this to LED devices, achieving maximum external quantum efficiency and luminance of 7.74% and 1022 cd m-2 with OPA treatment, as opposed to 3.59% and 229 cd m-2 for untreated CsPbBr3 NCs. This represents one of the highest efficiency LEDs obtained for all-inorganic CsPbBr3 NCs, accomplished through simple, effective passivation and purification processes. The robust binding of octylphosphonates to the perovskite lattice, and specifically their ability to interlink through hydrogen bonding, offers a promising passivation approach which could potentially be beneficial across a breadth of halide perovskite optoelectronic applications.
    Matched MeSH terms: Titanium
  11. Schiff base complex/TiO2 chemosensor for visual detection of food freshness level
    Sahudin MA, Su'ait MS, Tan LL, Abd Karim NH
    Spectrochim Acta A Mol Biomol Spectrosc, 2021 Mar 05;248:119129.
    PMID: 33281086 DOI: 10.1016/j.saa.2020.119129
    Histamine is one of the important biomarkers for food spoilage in the food sectors. In the present study, a rapid and simple analytical tool has been developed to detect histamine as an indirect strategy to monitor food freshness level. Optical histamine sensor with carboxyl-substituted Schiff base zinc(II) complex with hydroxypropoxy side chain deposited onto titanium dioxide nanoparticles was fabricated and was found to respond successfully to histamine. The Schiff base zinc(II) complex-histamine binding generated an enhancement of the fluorescent signal. Under the optimal reaction condition, the developed sensor can detect down to 2.53 × 10-10 M in the range of between 1.0 × 10-9 and 1.0 × 10-5 M (R2 = 0.9868). Selectivity performance of the sensor towards histamine over other amines was confirmed. The sensor also displayed good reproducibility performances with low relative standard deviation values (1.45%-4.95%). Shelf-life studies suggested that the developed sensor remains stable after 60 days in histamine detection. More importantly, the proposed sensor has been successfully applied to determine histamine in salmon fillet with good recoveries. This strategy has a promising potential in the food quality assurance sectors, especially in controlling the food safety for healthy consumption among consumers.
    Matched MeSH terms: Titanium*
  12. Sargassum myriocystum-mediated TiO2-nanoparticles and their antimicrobial, larvicidal activities and enhanced photocatalytic degradation of various dyes
    Balaraman P, Balasubramanian B, Liu WC, Kaliannan D, Durai M, Kamyab H, et al.
    Environ Res, 2022 Mar;204(Pt C):112278.
    PMID: 34757031 DOI: 10.1016/j.envres.2021.112278
    Recently, the phyco-synthesis of nanoparticles has been applied as a reliable approach to modern research field, and it has yielded a wide spectrum of diverse uses in fields such as biological science and environmental science. This study used marine natural resource seaweed Sargassum myriocystum due to their unique phytochemicals and their significant attributes in giving effective response on various biomedical applications. The response is created by their stress-tolerant environmental adaptations. This inspired us to make an attempt using the above-mentioned charactersitics. Therfore, the current study performed phycosynthesis of titanium dioxide nanoparticles (TiO2-NPs) utilising aqueous extracts of S. myriocystum. The TiO2-NPs formation was confirmed in earlier UV-visible spectroscopy analysis. The crystalline structure, functional groups (phycomolecules), particle morphology (cubic, square, and spherical), size (∼50-90 nm), and surface charge (negative) of the TiO2-NPs were analysed and confirmed by various characterisation analyses. In addition, the seaweed-mediated TiO2-NPs was investigated, which showed potential impacts on antibacterial activity and anti-biofilm actions against pathogens (Staphylococcus aureus, S. epidermidis, Escherichia coli, Proteus vulgaris, Pseudomonas aeruginosa, and Klebsiella pneumoniae). Additionally, some evaluations were performed on larvicidal activities of TiO2-NPs in oppose to Aedes aegypti and Culex quinquefasciatus mosquitos and the environmental effects of photocatalytic activities against methylene blue and crystal violet under sunlight irradiation. The highest percent of methylene blue degradation was observed at 92.92% within 45 min. Overall, our findings suggested that S. myriocystum mediates TiO2-NPs to be a potent disruptive material for bacterial pathogens and mosquito larvae and also to enhance the photocatalytic dye degradation.
    Matched MeSH terms: Titanium/chemistry
  13. Fulltext SYNTHESIS AND CHARACTERIZATION OF TiO2/ZnO-EPOXY BEADS AND THEIR PERFORMANCE FOR THE DEGRADATION OF DYE
    MOHAMAD HANIF AKMAL HUSSIN, WAN RAFIZAH WAN ABDULLAH, MOHAMAD AWANG
    UMT Journal of Undergraduate Research, 2020;2(2):9-14.
    MyJurnal
    Semiconductor oxides such as titanium dioxide (TiO2) and zinc oxide (ZnO) are used as the photocatalyst for removing contaminants. In addition, TiO2 and ZnO nanoparticles in the suspension form makes it difficult to be recovered and recycled. This study was conducted to investigate the efficiency of immobilizing TiO2 and ZnO nanoparticles in epoxy beads. The immobilization process using different ratios of photocatalysts TiO2/ZnO (1:0, 3:1, 1:1, 1:3 and 0:1) fixed on epoxy material. These epoxy beads were used for dye removal in photocatalysis using methylene blue (MB) solution at a concentration of 10mg/L. Besides, epoxy beads also characterized using scanning electron microscope (SEM), attenuated total reflection Fourier-transform infrared (ATR-FTIR) spectroscopy and thermogravimetric analysis (TGA). The results showed that the highly recommended epoxy bead is 3:1 ratio of TiO2/ZnO because it has good performance in dye degradation that proved from reducing concentration of MB to 2.4mg/L (76%). However, TiO2/ZnO characterization of 3:1 by SEM show on the surface the particle are found to be spherical in shape which is relatively high efficiency for the degradation, ATR-FTIR pattern in broad band 4000 cm-1 - 400cm-1 which correspond to hydroxyl stretching to be adsorbed at peak (474.49 cm-1 - 3722.61cm-1) respectively to the optimum for the degradation and TGA rate of change are 5mg to 2.5mg that residue (49.78%) due to decomposition or oxidation from mass loss. These findings are very effective and economical technique to be cost saving and highly efficient photocatalyst.
    Matched MeSH terms: Titanium
  14. Restoration of liquid effluent from oil palm agroindustry in Malaysia using UV/TiO2 and UV/ZnO photocatalytic systems: A comparative study
    Ng KH, Khan MR, Ng YH, Hossain SS, Cheng CK
    J Environ Manage, 2017 Jul 01;196:674-680.
    PMID: 28365553 DOI: 10.1016/j.jenvman.2017.03.078
    In this study, we have employed a photocatalytic method to restore the liquid effluent from a palm oil mill in Malaysia. Specifically, the performance of both TiO2 and ZnO was compared for the photocatalytic polishing of palm oil mill effluent (POME). The ZnO photocatalyst has irregular shape, bigger in particle size but smaller BET specific surface area (9.71 m2/g) compared to the spherical TiO2 photocatalysts (11.34 m2/g). Both scavenging study and post-reaction FTIR analysis suggest that the degradation of organic pollutant in the TiO2 system has occurred in the bulk solution. In contrast, it is necessary for organic pollutant to adsorb onto the surface of ZnO photocatalyst, before the degradation took place. In addition, the reactivity of both photocatalysts differed in terms of mechanisms, photocatalyst loading and also the density of photocatalysts. From the stability test, TiO2 was found to offer higher stability, as no significant deterioration in activity was observed after three consecutive cycles. On the other hand, ZnO lost around 30% of its activity after the 1st-cycle of photoreaction. The pH studies showed that acidic environment did not improve the photocatalytic degradation of the POME, whilst in the basic environment, the reaction media became cloudy. In addition, longevity study also showed that the TiO2 was a better photocatalyst compared to the ZnO (74.12%), with more than 80.0% organic removal after 22 h of UV irradiation.
    Matched MeSH terms: Titanium*
  15. Response surface methodology and artificial neural network for remediation of acid orange 7 using TiO2-P25: optimization and modeling approach
    Zulfiqar M, Chowdhury S, Omar AA, Siyal AA, Sufian S
    Environ Sci Pollut Res Int, 2020 Sep;27(27):34018-34036.
    PMID: 32557068 DOI: 10.1007/s11356-020-09674-4
    The primary responsibility for continuously discharging toxic organic pollutants into water bodies and open environments is the increase in industrial and agricultural activities. Developing economical and suitable methods to continuously remove organic pollutants from wastewater is highly essential. The aim of the present research was to apply response surface methodology (RSM) and artificial neural networks (ANNs) for optimization and modeling of photocatalytic degradation of acid orange 7 (AO7) by commercial TiO2-P25 nanoparticles (TNPs). Dose of TNPs, pH, and AO7 concentration were selected as investigated parameters. RSM results reveal the reflective rate of AO7 removal of ~ 94.974% was obtained at pH 7.599, TNP dose of 0.748 g/L, and AO7 concentration of 28.483 mg/L. The resulting quadratic model is satisfactory with the highest coefficient of determination (R2) between the predicted and experimental data (R2 = 0.98 and adjusted R2 = 0.954). On the other hand, ANNs were successfully employed for modeling of AO7 degradation process. The proposed ANN model was absolutely fitted with experimental results producing the highest R2. Furthermore, root mean square error (RMSE), mean average deviation (MAD), absolute average relative error (AARE), and mean square error (MSE) were examined more to compare the predictive capabilities of ANN and RSM models. The experimental data was well fitted into pseudo-first-order and pseudo-second-order kinetics with more accuracy. Thermodynamic parameters, namely enthalpy, entropy, Gibbs' free energy, and activation energy, were also evaluated to suggest the nature of the degradation process. The increase of temperature was analyzed to be more suitable for the fast removal of AO7 over TNPs. Graphical abstract.
    Matched MeSH terms: Titanium
  16. Fulltext Resistance Switching Behavior in Rectangle-Nano-Pattern SrTiO3 Induced by Simple Annealing
    Liao X, Zhang Y, Wang J, Kang J, Zhang J, Wang J, et al.
    Materials (Basel), 2019 Nov 09;12(22).
    PMID: 31717524 DOI: 10.3390/ma12223698
    The tunability of semi-conductivity in SrTiO3 single crystal substrates has been realized by a simple encapsulated annealing method under argon atmosphere. This high temperature annealing-induced property changes are characterized by the transmission spectra, scanning electron microscopy (SEM) and synchrotron-based X-ray absorption (XAS). We find the optical property is strongly influenced by the annealing time (with significant decrease of transmittance). A sub gap absorption at ~427 nm is detected which is attributed to the introduction of oxygen vacancy. Interestingly, in the SEM images, annealing-induced regularly rectangle nano-patterns are directly observed which is contributed to the conducting filaments. The XAS of O K-edge spectra shows the changes of electronic structure by annealing. Very importantly, resistance switching response is displayed in the annealed SrTiO3 single crystal. This suggests a possible simplified route to tune the conductivity of SrTiO3 and further develop novel resistance switching materials.
    Matched MeSH terms: Titanium
  17. Fulltext Removal of reactive red 4 dye using chitosan-epichlorohydrin/ TiO2 nanocomposite: application of response surface methodology
    Ibrahim Awad Mohammed, Abdallah Reghioua, Emad Yousif, Ali H. Jawad, Nurul Najwa Abd Malek
    Science Letters, 2020;14(1):96-108.
    MyJurnal
    Chitosan-epichlorohydrin/TiO2 composite was synthesized to be employed as an adsorbent for the
    removal of reactive red 4 (RR4) dye from aqueous solution. Response surface methodology (RSM) with 3-level Box-Behnken design (BBD) was utilized for the optimization of the removal of RR4. The process key variables which include adsorbent dose (A: 0.5 – 1.5 g), pH (B: 4 – 10) and time (30 – 80 min) were selected for the optimization process. The experimental data for RR4 removal were statistically analysed using analysis of variance (ANOVA). The significant interaction between key parameters on RR4 removal efficiency was observed by interaction between AB and AC. The highest RR4 removal (95.08%) was obtained under the following conditions; adsorbent dose (1.0 g), pH 4 and time of 80 min.
    Matched MeSH terms: Titanium
  18. Removal of dyes using immobilized titanium dioxide illuminated by fluorescent lamps
    Zainal Z, Hui LK, Hussein MZ, Taufiq-Yap YH, Abdullah AH, Ramli I
    J Hazard Mater, 2005 Oct 17;125(1-3):113-20.
    PMID: 15996813
    The photodegradation of various dyes in aqueous solution was studied. Experiments were carried out using glass coated titanium dioxide thin film as photocatalyst. Photodegradation processes of methylene blue (MB), methyl orange (MO), indigo carmine (IC), chicago sky blue 6B (CSB), and mixed dye (MD, mixture of the four mentioned single dye) were reported. As each photodegradation system is pH dependent, the photodegradation experiment was carried out in each dye photodegradation reactive pH range at approximately 28 degrees C. The dyes removal efficiency was studied and compared using UV-vis spectrophotometer analysis. The total removal of each dye was: methylene blue (90.3%), methyl orange (98.5%), indigo carmine (92.4%), chicago sky blue 6B (60.3%), and mixed dyes (70.1%), respectively. The characteristic of the photocatalyst was investigated using X-ray diffractometer (XRD). The amount of each dye intermediate produced in the photodegradation process was also determined with the help of total organic carbon (TOC) analysis.
    Matched MeSH terms: Titanium*
  19. Removal of VOCs from gas streams with double perovskite-type catalysts
    Pan KL, Pan GT, Chong S, Chang MB
    J Environ Sci (China), 2018 Jul;69:205-216.
    PMID: 29941256 DOI: 10.1016/j.jes.2017.10.012
    Double perovskite-type catalysts including La2CoMnO6 and La2CuMnO6 are first evaluated for the effectiveness in removing volatile organic compounds (VOCs), and single perovskites (LaCoO3, LaMnO3, and LaCuO3) are also tested for comparison. All perovskites are tested with the gas hourly space velocity (GHSV) of 30,000hr-1, and the temperature range of 100-600°C for C7H8 removal. Experimental results indicate that double perovskites have better activity if compared with single perovskites. Especially, toluene (C7H8) can be completely oxidized to CO2 at 300°C as La2CoMnO6 is applied. Characterization of catalysts indicates that double perovskites own unique surface properties and are of higher amounts of lattice oxygen, leading to higher activity. Additionally, apparent activation energy of 68kJ/mol is calculated using Mars-van Krevelen model for C7H8 oxidation with La2CoMnO6 as catalyst. For durability test, both La2CoMnO6 and La2CuMnO6 maintain high C7H8 removal efficiencies of 100% and 98%, respectively, at 300°C and 30,000hr-1, and they also show good resistance to CO2 (5%) and H2O(g) (5%) of the gas streams tested. For various VOCs including isopropyl alcohol (C3H8O), ethanal (C2H4O), and ethylene (C2H4) tested, as high as 100% efficiency could be achieved with double perovskite-type catalysts operated at 300-350°C, indicating that double perovskites are promising catalysts for VOCs removal.
    Matched MeSH terms: Titanium/chemistry*
  20. Regenerated cellulose membrane as bio-template for in-situ growth of visible-light driven C-modified mesoporous titania
    Mohamed MA, W Salleh WN, Jaafar J, Mohd Hir ZA, Rosmi MS, Abd Mutalib M, et al.
    Carbohydr Polym, 2016 08 01;146:166-73.
    PMID: 27112862 DOI: 10.1016/j.carbpol.2016.03.050
    Visible light driven C-doped mesoporous TiO2 (C-MTiO2) nanorods have been successfully synthesized through green, low cost, and facile approach by sol-gel bio-templating method using regenerated cellulose membrane (RCM) as nanoreactor. In this study, RCM was also responsible to provide in-situ carbon sources for resultant C-MTiO2 nanorods in acidified sol at low temperatures. The composition, crystallinity, surface area, morphological structure, and optical properties of C-MTiO2 nanorods, respectively, had been characterized using FTIR, XRD, N2 adsorption/desorption, TEM, UV-vis-NIR, and XPS spectroscopy. The results suggested that the growth of C-MTiO2 nanorods was promoted by the strong interaction between the hydroxyl groups of RCMs and titanium ion. Optical and XPS analysis confirmed that carbon presence in TiO2 nanorods were responsible for band-gap narrowing, which improved the visible light absorption capability. Photocatalytic activity measurements exhibited the capability of C-MTiO2 nanorods in degradation of methyl orange in aqueous solution, with 96.6% degradation percentage under visible light irradiation.
    Matched MeSH terms: Titanium/chemistry*
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