Displaying publications 81 - 100 of 117 in total

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  1. Maqbool M, Tirmazi SSM, Shakoor A, Akram Z, Nazir R, Chohan AN, et al.
    Biomed Res Int, 2023;2023:1044541.
    PMID: 36845639 DOI: 10.1155/2023/1044541
    BACKGROUND: Despite of having improved endodontic file designs as well as the reinforced metal alloy file structure, intracanal endodontic file separation (EFS) is still a very problematic and worrisome dental incident, which usually occurs without any visible signs of permanent deformation. Further, there have been conflicting reports regarding the clinical significance of leaving separated files within root canals.

    AIMS: The aim of this study was to look into the current perceptions and awareness about file separation during endodontic treatment among the dental house officers (DHOs).

    MATERIALS AND METHODS: A novel validated questionnaire comprising of 15 close-ended questions was distributed anonymously via Google Forms through email to 1100 DHOs across Pakistan. The questionnaire consisted of two parts: the first component (Section I) collected demographic data and the second component (Section II) investigated the causes of EFS during root canal treatment. Following the completion of socioeconomic information, including age and gender, the DHOs were asked to answer a few questions about the various reasons for endodontic instrument fracture.

    RESULTS: A total of 800 responses were recorded, with an effective rate of 72.8%. The majority of the DHOs (p value < 0.001) perceived that endodontic instrument fracture occurred in the posterior (61.5%) and apical third of the canal (50.5%) and in older permanent dentition (67.3%), possibly due to patient anxiety (62%). Better choice of instrument (61.15%), operators' experience (95.3%), knowledge (87.5%), and proper root canal cleaning (91.1%) are believed to be the vital steps in reducing endodontic file separation/fracture. Furthermore, majority of them (p value < 0.001) perceived that stainless steel was a superior alloy for filing instruments. Manual files tend to be more prone to fractures due to repeated use than rotary files.

    CONCLUSION: This study demonstrated that young DHOs had adequate knowledge and awareness regarding the potential predisposing factors and handling techniques for EFS. This study thereby provides an evaluating tool to access the insights of the current perceptions and awareness of DHOs concerning EFS.

    Matched MeSH terms: Titanium/chemistry
  2. Ling CM, Mohamed AR, Bhatia S
    Chemosphere, 2004 Nov;57(7):547-54.
    PMID: 15488916
    TiO2 thin film photocatalyst was successfully synthesized and immobilized on glass reactor tube using sol-gel method. The synthesized TiO2 coating was transparent, which enabled the penetration of ultra-violet (UV) light to the catalyst surface. Two photocatalytic reactors with different operating modes were tested: (a) tubular photocatalytic reactor with re-circulation mode and (b) batch photocatalytic reactor. A new proposed TiO2 synthesized film formulation of 1 titanium isopropoxide: 8 isopropanol: 3 acetyl acetone: 1.1 H2O: 0.05 acetic acid (in molar ratio) gave excellent photocatalytic activity for degradation of phenol and methylene blue dye present in the water. The half-life time, t1/2 of photocatalytic degradation of phenol was 56 min at the initial phenol concentration of 1000 microM in the batch reactor. In the tubular photocatalytic reactor, 5 re-circulation passes with residence time of 2.2 min (single pass) degraded 50% of 40-microM methylene blue dye. Initial phenol concentration, presence of hydrogen peroxide, presence of air bubbling and stirring speed as the process variables were studied in the batch reactor. Initial methylene blue concentration, pH value, light intensity and reaction temperature were studied as the process variables in the tubular reactor. The synthesized TiO2 thin film was characterized using SEM, XRD and EDX analysis. A comparative performance between the synthesized TiO2 thin film and commercial TiO2 particles (99% anatase) was evaluated under the same experimental conditions. The TiO2 film was equally active as the TiO2 powder catalyst.
    Matched MeSH terms: Titanium/chemistry*
  3. Baig U, Gondal MA, Alam MF, Wani WA, Younus H
    J. Photochem. Photobiol. B, Biol., 2016 Nov;164:244-255.
    PMID: 27710872 DOI: 10.1016/j.jphotobiol.2016.09.034
    Cancer and pathogenic microbial diseases have terribly affected human health over a longer period of time. In response to the increasing casualties due to cancer and microbial diseases, unique poly(3-methylthiophene) and poly(3-methylthiophene)-titanium(IV)phosphate composite were prepared via in-situ oxidative chemical polymerization in this work. The poly(3-methylthiophene) and poly(3-methylthiophene)-titanium(IV)phosphate composite were well characterized by Fourier transform infrared spectroscopy and field emission scanning electron microscopy. DNA binding studies by UV-Visible and fluorescence spectroscopic investigations indicated strong binding affinities of poly(3-methylthiophene) and poly(3-methylthiophene)-titanium(IV)phosphate nanocomposite; leading to structural damage of DNA. Poly(3-methylthiophene)-titanium(IV)phosphate nanocomposite showed stronger interactions with DNA as compared to poly(3-methylthiophene) and from dye displacement assay it was confirmed that mode of binding of both the formulations was intercalative. The antimicrobial screening revealed that polymer and its composite displayed stronger antibacterial effects than ampicillin against Bacillus subtilis, Staphylococcus aureus, Pseudomonas aeruginosa and Salmonella typhimurium. Besides, the poly(3-methylthiophene) and poly(3-methylthiophene)-titanium(IV)phosphate nanocomposite showed dose dependent effects towards estrogen receptor positive breast cancer (MCF-7) and estrogen receptor negative breast cancer (MDA-MB-231) cell lines; with poly(3-methylthiophene)-titanium(IV)phosphate nanocomposite showing better activities against both cell lines. In all in-vitro biological investigations, poly(3-methylthiophene)-titanium(IV)phosphate composite showed superior properties to that of the pure poly(3-methylthiophene), which encouraged us to suggest its potential as future therapeutic gear in drug delivery and other allied fields.
    Matched MeSH terms: Titanium/chemistry
  4. Riaz N, Bustam MA, Chong FK, Man ZB, Khan MS, Shariff AM
    ScientificWorldJournal, 2014;2014:342020.
    PMID: 25105158 DOI: 10.1155/2014/342020
    Bimetallic Cu-Ni/TiO2 photocatalysts were synthesized using wet impregnation (WI) method with TiO2 (Degussa-P25) as support and calcined at different temperatures (180, 200, and 300°C) for the photodegradation of DIPA under visible light. The photocatalysts were characterized using TGA, FESEM, UV-Vis diffuse reflectance spectroscopy, fourier transform infrared spectroscopy (FTIR) and temperature programmed reduction (TPR). The results from the photodegradation experiments revealed that the Cu-Ni/TiO2 photocatalysts exhibited much higher photocatalytic activities compared to bare TiO2. It was found that photocatalyst calcined at 200°C had the highest photocatalyst activities with highest chemical oxygen demand (COD) removal (86.82%). According to the structural and surface analysis, the enhanced photocatalytic activity could be attributed to its strong absorption into the visible region and high metal dispersion.
    Matched MeSH terms: Titanium/chemistry*
  5. Subramonian W, Wu TY, Chai SP
    J Environ Manage, 2017 Feb 01;187:298-310.
    PMID: 27914351 DOI: 10.1016/j.jenvman.2016.10.024
    In this work, heterogeneous photocatalysis was used to treat pulp and paper mill effluent (PPME). Magnetically retrievable Fe2O3-TiO2 was fabricated by employing a solvent-free mechanochemical process under ambient conditions. Findings elucidated the successful incorporation of Fe2O3 into the TiO2 lattice. Fe2O3-TiO2 was found to be an irregular and slightly agglomerated surface morphology. In comparison to commercial P25, Fe2O3-TiO2 exhibited higher ferromagnetism and better catalyst properties with improvements in surface area (58.40 m2/g), pore volume (0.29 cm3/g), pore size (18.52 nm), and band gap (2.95 eV). Besides, reusability study revealed that Fe2O3-TiO2 was chemically stable and could be reused successively (five cycles) without significant changes in its photoactivity and intrinsic properties. Additionally, this study demonstrated the potential recovery of Fe2O3-TiO2 from an aqueous suspension by using an applied magnetic field or sedimentation. Interactive effects of photocatalytic conditions (initial effluent pH, Fe2O3-TiO2 dosage, and air flow-rate), reaction mechanism, and the presence of chemical oxidants (H2O2, BrO3-, and HOCl) during the treatment process of PPME were also investigated. Under optimal conditions (initial effluent pH = 3.88, [Fe2O3-TiO2] = 1.3 g/L, and air flow-rate = 2.28 L/min), the treatment efficiency of Fe2O3-TiO2 was 98.5% higher than the P25. Based on Langmuir-Hinshelwood kinetic model, apparent rate constants of Fe2O3-TiO2 and P25 were 9.2 × 10-3 and 2.7 × 10-3 min-1, respectively. The present study revealed not only the potential of using magnetic Fe2O3-TiO2 in PPME treatment but also demonstrated high reusability and easy separation of Fe2O3-TiO2 from the wastewater.
    Matched MeSH terms: Titanium/chemistry
  6. Ramli ZA, Asim N, Isahak WN, Emdadi Z, Ahmad-Ludin N, Yarmo MA, et al.
    ScientificWorldJournal, 2014;2014:415136.
    PMID: 25013855 DOI: 10.1155/2014/415136
    This study involves the investigation of altering the photocatalytic activity of TiO2 using composite materials. Three different forms of modified TiO2, namely, TiO2/activated carbon (AC), TiO2/carbon (C), and TiO2/PANi, were compared. The TiO2/carbon composite was obtained by pyrolysis of TiO2/PANi prepared by in situ polymerization method, while the TiO2/activated carbon (TiO2/AC) was obtained after treating TiO2/carbon with 1.0 M KOH solution, followed by calcination at a temperature of 450°C. X-ray powder diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared (FTIR), thermogravimetric analysis (TG-DTA), Brunauer-Emmet-Teller (BET), and UV-Vis spectroscopy were used to characterize and evaluate the prepared samples. The specific surface area was determined to be in the following order: TiO2/AC > TiO2/C > TiO2/PANi > TiO2 (179 > 134 > 54 > 9 m(2) g(-1)). The evaluation of photocatalytic performance for the degradation of methylene blue under UV light irradiation was also of the same order, with 98 > 84.7 > 69% conversion rate, which is likely to be attributed to the porosity and synergistic effect in the prepared samples.
    Matched MeSH terms: Titanium/chemistry*
  7. Lam SM, Sin JC, Abdullah AZ, Mohamed AR
    Environ Technol, 2013 May-Jun;34(9-12):1097-106.
    PMID: 24191441
    In the work presented here, photocatalytic systems using TiO2 and ZnO suspensions were utilized to evaluate the degradation of resorcinol (ReOH). The effects of catalyst concentration and solution pH were investigated and optimized using multivariate analysis based on response surface methodology. The results indicated that ZnO showed greater degradation and mineralization activities compared to TiO2 under optimized conditions. Using certain radical scavengers, a positive hole, together with the participation of hydroxyl radicals, were the oxidative species responsible for ReOH degradation on TiO2 whereas, the ZnO photocatalysis occurred principally via hydroxyl radicals. Some hitherto unreported pathway intermediates of ReOH degradation were identified using gas chromatography-mass spectrometry. A tentative reaction mechanism for the formation of these intermediates was proposed. Moreover, the figure-of-merit electrical energy per order was employed to estimate the electrical energy consumption.
    Matched MeSH terms: Titanium/chemistry*
  8. Arifin SNH, Radin Mohamed RMS, Al-Gheethi A, Lai CW, Gopalakrishnan Y, Hairuddin ND, et al.
    Environ Sci Pollut Res Int, 2023 Feb;30(10):25103-25118.
    PMID: 34617227 DOI: 10.1007/s11356-021-16732-y
    The current work aimed to investigate the degradation of the triclocarban (TCC) in aqueous solution using a modified zeolite/TiO2 composite (MZTC) synthesized by applying the electrochemical anodization (ECA). The synthesis process was conducted at different voltages (10, 40, and 60) V in 1 h and using electrophoresis deposition (EPD) in doping zeolite. The MZTC was covered with the array ordered, smooth and optimum elongated nanotubes with 5.1 μm of the length, 120.3 nm of the inner diameter 14.5 nm of the wall thickness with pure titanium and crystalline titania as determined by FESEM/EDS, and XRD. The kinetic study by following Langmuir-Hinshelwood(L-H) model and pseudo first order, the significant constant rate was obtained at pH 11 which was 0.079 ppm/min, 0.75 cm2 of MZTC catalyst loading size achieved 0.076 ppm/min and 5 ppm of TCC initial concentration reached 0.162 ppm/min. The high-performance liquid chromatography (HPLC) analysis for mechanism study of TCC photocatalytic degradation revealed eleven intermediate products after the whole process of photocatalysis. In regard of toxicology assessment by the bacteria which is Photobacterium phosphoreum, the obtained concentration of TCC at minute 60 was less satisfied with remained 0.36 ppm of TCC was detected indicates that the concentration was above allowable level. Where the allowable level of TCC in stream is 0.1 ppm.
    Matched MeSH terms: Titanium/chemistry
  9. Dzinun H, Othman MHD, Ismail AF
    Chemosphere, 2019 Aug;228:241-248.
    PMID: 31035161 DOI: 10.1016/j.chemosphere.2019.04.118
    Comparison studies in suspension and hybrid photocatalytic membrane reactor (HPMR) system was investigated by using Reactive Black 5 (RB5) as target pollutant under UVA light irradiation. To achieve this aim, hybrid TiO2/clinoptilolite (TCP) photocatalyst powder was prepared by solid-state dispersion (SSD) methods and embedded at the outer layer of dual layer hollow fiber (DLHF) membranes fabricated via single step co-spinning process. TiO2 and CP photocatalyst were also used as control samples. The samples were characterized by Scanning Electron Microscopy (SEM), Energy Dispersion of X-ray (EDX), X-ray diffraction (XRD) and Brunauer-Emmett-Teller (BET) analyses. The result shows that TCP was actively functioned as photocatalyst in suspension system and 86% of RB5 photocatalytic degradation achieved within 60 min; however the additional step is required to separate the catalyst with treated water. In the HPMR system, even though the RB5 photocatalytic degradation exhibits lower efficiency however the rejection of RB5 was achieved up to 95% under UV irradiation due to the properties of photocatalytic membranes. The well dispersed of TCP at the outer layer of DLHF membrane have improved the surface affinity of DL-TCP membrane towards water, exhibit the highest pure water flux of 41.72 L/m2.h compared to DL-TiO2 membrane. In general, CP can help on improving photocatalytic activity of TiO2 in suspension, increased the RB5 removal and the permeability of DLHF membrane in HPMR system as well.
    Matched MeSH terms: Titanium/chemistry*
  10. Saepurahman, Abdullah MA, Chong FK
    J Hazard Mater, 2010 Apr 15;176(1-3):451-8.
    PMID: 19969415 DOI: 10.1016/j.jhazmat.2009.11.050
    Tungsten-loaded TiO(2) photocatalyst has been successfully prepared and characterized. TEM analysis showed that the photocatalysts were nanosize with the tungsten species forming layers of coverage on the surface of TiO(2), but not in clustered form. This was confirmed by XRD and FT-Raman analyses where tungsten species were well dispersed at lower loading (<6.5 mol%), but were in crystalline WO(3) at higher loadings (>12 mol%). In addition, loading with tungsten could stabilize the anatase phase from transforming into inactive rutile phase and did not shift the optical absorption to the visible region as shown by DRUV-vis analysis. PZC value of TiO(2) was found at 6.4, but the presence of tungsten at 6.5 mol% WO(3), decreased the PZC value to 3. Tungsten-loaded TiO(2) was superior to unmodified TiO(2) with 2-fold increase in degradation rate of methylene blue, and equally effective for the degradation of different class of dyes such as methyl violet and methyl orange at 1 mol% WO(3) loading.
    Matched MeSH terms: Titanium/chemistry*
  11. Hosseini M, Fazelian N, Fakhri A, Kamyab H, Yadav KK, Chelliapan S
    J. Photochem. Photobiol. B, Biol., 2019 May;194:128-134.
    PMID: 30953914 DOI: 10.1016/j.jphotobiol.2019.03.016
    NiS-SiO2 and Cr2S3-TiO2 synthesized by Ultrasound-Microwave method was tested for the photo-degradation of methyl red as azo dye under ultraviolet (UV) light. The structure and morphology of the synthesized materials were examined through scanning electron microscopy, X-ray diffraction and photoelectron spectroscopy, energy-dispersive spectroscopy, dynamic light scattering and the band gap energy differences were determined through diffuse reflectance spectroscopy (DRS). The crystallite size and band gap values of SiO2, TiO2, NiS-SiO2 and Cr2S3-TiO2-1 were obtained from XRD and UV-vis DRS analysis and found insignificant 44.22, 54.11, and 57.11 nm, and 8.9, 3.2, 3.0, 2.7 eV, respectively. The NiS-SiO2 and Cr2S3-TiO2 nanocomposites exhibited good stability and catalytic performance in the azo dye degradation; the composite provides a complete degradation after 50 min under UV irradiation. The effects of different quencher compounds on the Methyl red dye degradation were also investigated. The result for this experiment shows the system without the quencher was highly degradation of Methyl red. The antibacterial influence of the SiO2, TiO2, NiS-SiO2 and Cr2S3-TiO2-1 were studied versus two species bacteria. The antifungal performance of this nanoparticle was analyzed versus two species fungi as the C. albicans and P. funiculosum. Biological data demonstrated that the prepared catalyst has great bactericidal and fungicidal properties.
    Matched MeSH terms: Titanium/chemistry*
  12. Tan AW, Tay L, Chua KH, Ahmad R, Akbar SA, Pingguan-Murphy B
    Int J Nanomedicine, 2014;9:5389-401.
    PMID: 25473278 DOI: 10.2147/IJN.S72659
    Two important criteria of an ideal biomaterial in the field of stem cells research are to regulate the cell proliferation without the loss of its pluripotency and to direct the differentiation into a specific cell lineage when desired. The present study describes the influence of TiO2 nanofibrous surface structures on the regulation of proliferation and stemness preservation of adipose-derived stem cells (ADSCs). TiO2 nanofiber arrays were produced in situ onto Ti-6Al-4V substrate via a thermal oxidation process and the successful fabrication of these nanostructures was confirmed by field emission scanning electron microscopy (FESEM), energy dispersive spectrometer (EDS), X-ray diffractometer (XRD), and contact angle measurement. ADSCs were seeded on two types of Ti-6Al-4V surfaces (TiO2 nanofibers and flat control), and their morphology, proliferation, and stemness expression were analyzed using FESEM, AlamarBlue assay, flow cytometry, and quantitative real-time polymerase chain reaction (qRT-PCR) after 2 weeks of incubation, respectively. The results show that ADSCs exhibit better adhesion and significantly enhanced proliferation on the TiO2 nanofibrous surfaces compared to the flat control surfaces. The greater proliferation ability of TiO2 nanofibrous surfaces was further confirmed by the results of cell cycle assay. More importantly, TiO2 nanofibrous surfaces significantly upregulate the expressions of stemness markers Sox-2, Nanog3, Rex-1, and Nestin. These results demonstrate that TiO2 nanofibrous surfaces can be used to enhance cell adhesion and proliferation while simultaneously maintaining the stemness of ADSCs, thereby representing a promising approach for their potential application in the field of bone tissue engineering as well as regenerative therapies.
    Matched MeSH terms: Titanium/chemistry*
  13. Jukapli NM, Bagheri S
    J. Photochem. Photobiol. B, Biol., 2016 Oct;163:421-30.
    PMID: 27639172 DOI: 10.1016/j.jphotobiol.2016.08.046
    This review provides a background, fundamental and advanced application of titania nanoparticles (TiO2) on the disinfection and killing of cancer cell through photocatalytic chemistry. It starts with the characteristic properties focused on the surface, light sensitivity, crystallinity and toxicology of TiO2 as a photocatalyst. Consequently, outline and design of photocatalytic reactor has been figured out based on the target organisms, including bacteria, viruses, fungi and cancer cells. Despite a large number of studies undertaken, limited selectivity and efficacy of TiO2 photocatalyst are still widely accepted problems. An ideal TiO2 photocatalyst should have the combined properties of highly stable reactive oxygen species yield and a greater degree of selectivity towards cancerous cell without damaging the healthy tissues. Hybridization of TiO2 with metal, metal oxide and carbon nano materials significantly improved both of stability and selectivity of TiO2, whilst maintaining its high Photodynamic reactivity.
    Matched MeSH terms: Titanium/chemistry*
  14. 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*
  15. 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*
  16. 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
  17. 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
  18. 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*
  19. Elshereksi NW, Ghazali MJ, Muchtar A, Azhari CH
    J Dent, 2017 Jan;56:121-132.
    PMID: 27916635 DOI: 10.1016/j.jdent.2016.11.012
    OBJECTIVES: This study aimed to fabricate and characterise silanated and titanated nanobarium titanate (NBT) filled poly(methyl methacrylate) (PMMA) denture base composites and to evaluate the behaviour of a titanate coupling agent (TCA) as an alternative coupling agent to silane. The effect of filler surface modification on fracture toughness was also studied.

    METHODS: Silanated, titanated and pure NBT at 5% were incorporated in PMMA matrix. Neat PMMA matrix served as a control. NBT was sonicated in MMA prior to mixing with the PMMA. Curing was carried out using a water bath at 75°C for 1.5h and then at 100°C for 30min. NBT was characterised via Fourier transform-infrared spectroscopy (FTIR), Transmission Electron Microscopy (TEM) and Brunauer-Emmett-Teller (BET) analysis before and after surface modification. The porosity and fracture toughness of the PMMA nanocomposites (n=6, for each formulation and test) were also evaluated.

    RESULTS: NBT was successfully functionalised by the coupling agents. The TCA exhibited the lowest percentage of porosity (0.09%), whereas silane revealed 0.53% porosity. Statistically significant differences in fracture toughness were observed among the fracture toughness values of the tested samples (p<0.05). While the fracture toughness of untreated samples was reduced by 8%, an enhancement of 25% was achieved after titanation. In addition, the fracture toughness of the titanated samples was higher than the silanated ones by 10%.

    CONCLUSION: Formation of a monolayer on the surface of TCA enhanced the NBT dispersion, however agglomeration of silanated NBT was observed due to insufficient coverage of NBT surface. Such behaviour led to reducing the porosity level and improving fracture toughness of titanated NBT/PMMA composites. Thus, TCA seemed to be more effective than silane.

    CLINICAL SIGNIFICANCE: Minimising the porosity level could have the potential to reduce fungus growth on denture base resin to be hygienically accepTable Such enhancements obtained with Ti-NBT could lead to promotion of the composites' longevity.

    Matched MeSH terms: Titanium/chemistry*
  20. Daood U, Bandey N, Qasim SB, Omar H, Khan SA
    Acta Odontol Scand, 2011 Nov;69(6):367-73.
    PMID: 21449690 DOI: 10.3109/00016357.2011.569507
    To investigate the failure of 15 dental implants (Paragon/Zimmer) in relation to their surface quality.
    Matched MeSH terms: Titanium/chemistry*
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