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Query: KEGG:D01931 (TiO2)
 11,320 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Several methods, including changing electrolyte concentration, temperature, stirring, and voltage were studied to improve the degradation effect of electrochemical treatment in dye wastewater. In addition, nanophase TiO2 catalyst and Co-Bi-PbO2/Ti anode have been prepared to expedite color removal. Enhancement of temperature leads to proportional increase of color removal. As for voltage, at low levels its increase could greatly improves color removal. After voltage reaches about 3.0 V, its improvement effect declines quickly. The influence of electrolyte concentration and aerating on color removal are similar to that of voltage. So it favored to degrade organic pollutants using high salt concentration, high voltages and large electric current to improve treatment effect. However, the efficiency of energy supplied during electrolysis decreases. A nonlinear model is established to evaluate the influence of electrolyte concentration and voltage on color removal. The model agrees with the experiment data very well. It is suggested by the simulation result of this model that electrolysis degradation should better be carried out at about 3.0 V, in 0.01 M Na2SO4 concentration for high energy efficiency. Additionally, either catalyst or Co-Bi-PbO2/Ti anode brings about 0.15 times more color removal without increasing electric current. Together, they could bring forth some 0.22 times higher color removal.
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PMID:Methods to improve electrochemical treatment effect of dye wastewater. 1630 Aug 85

Four resorbable phosphate invert glasses for use as bone replacement were synthesized in the system P2O5--CaO--MgO--Na2O. TiO2 and SiO2 were added at concentrations of 1 and 5.5 mol % to control solubility and crystallization. Both bulk glasses and samples with an open porosity of 65% and pore sizes of 150 to 400 microm were produced using a salt sintering process. Addition of TiO2 decreased the solubility in water and simulated body fluid, while the glass with addition of SiO2 showed a higher dissolution rate than did the original glass. The hypothesis that dissolution rates of the glasses will affect cell proliferation of osteoblastlike cells was tested using a MC3T3-E1.4 murine preosteoblast cell line. Cells were cultured on nonporous polished and porous glasses with tissue culture polystyrene (TCPS) as control. Cell proliferation was studied over 24 and 72 h in culture. Cells proliferated on all polished glasses, but proliferation on porous glasses showed variations with glass composition. Cell proliferation increased with decreased solubility of the glass. It is suggested that resorbable implant materials require the adjustment of dissolution rate so as to facilitate cell adhesion and proliferation and thus a gradual transition from artificial implant to new bone structure.
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PMID:Effect of degradation rates of resorbable phosphate invert glasses on in vitro osteoblast proliferation. 1639 27

Ionic liquids containing the nitrile and vinyl functional groups attached to imidazolium cations combined with various anions, e.g., iodide, bis[(trifluoromethyl)sulfonyl]imide ([TFSI]-), or dicyanamide ([N(CN)2]-), have been prepared and characterized. These ionic liquids have been successfully used as electrolytes for dye-sensitized solar cells based on nanocrystalline TiO2 with the amphiphilic ruthenium sensitizer [ruthenium (4,4'-dicarboxylic acid-2,2'-bipyridine)(4,4'-bis(p-hexyloxystyryl)-2,2'-bipyridine)][NCS]2 (coded K-19). The iodide salt was used in 3-methoxypropionitrile-based electrolytes, and the performances of both types of devices were evaluated on the basis of their photocurrent density-voltage characteristics and dark current measurements, demonstrating that the functional groups do not exert a detrimental effect on the performance. The solid-state structure of the nitrile-functionalized salt [C1C3CN(im)]I has also been established by single-crystal X-ray diffraction, revealing extensive hydrogen bonding between the cation protons and the iodide.
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PMID:Influence of ionic liquids bearing functional groups in dye-sensitized solar cells. 1647 69

The feasibility study of the application of the photoelectrocatalytic decontamination of high saline produced water containing refractory organic pollutants was investigated in the slurry photoelectrocatalytic reactor with nanometer TiO2 particle prepared with sol-gel method using the acetic acid as hydrolytic catalyst. The efficiency of the photoelectrocatalytic decontamination of produced water was determined with both COD removal from the tested wastewater and the decrease of mutagenic activity evaluated by Ames tests. The experimental results showed that the photoelectrocatalysis is a quite efficient process for decontaminating the produced water, although there are high concentration of salt existed in oilfield wastewater. We found that the COD removal efficiencies by photoelectrocatalytic process are much higher than that of by photocatalytic or electrochemical oxidation individually in the photoelectrocatalytic reactor. The COD removal can be substantially improved by the added H2O2 and the generation of active chlorine from high concentration chlorides in the wastewater. The effects of various operating conditions, such as initial COD concentration, applied cell voltage, catalyst amount and initial pH value of solution, on the photoelectrocatalytic efficiencies, is also investigated in detail. The results showed that when the raw produced wastewater was diluted in a 1:1 (v/v) ratio, there is a highest COD removal efficiency. And the photoelectrocatalytic degradation of organic pollutants in saline water is much favored in acidic solution than that in neutral and/or alkaline solution.
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PMID:Photoelectrocatalytic decontamination of oilfield produced wastewater containing refractory organic pollutants in the presence of high concentration of chloride ions. 1687 77

In this communication, TiO2 nanocrystalline thin films synthesized by a room temperature (27 degrees C) chemical dip process. To our knowledge, this is first report of the preparation of nanoscale rutile TiO2 particles from common inorganic salt at such low temperature. Interestingly, unprecedented dynamic color change accompanies with titanium dioxide grain size, which can be seen with the naked eye that generated curiosity in our mind to check UV-vis absorption, where significant changes were observed. The room temperature synthesized thin films of rutile titanium dioxide make it a potential candidate for high-compatibility material, which can be used in artificial heart valves.
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PMID:Unprecedented coloration of rutile titanium dioxide nanocrystalline thin films. 1693 Oct 31

Degradable porous composite materials for use as temporary bone replacement or tissue engineering scaffolds were produced using a methacrylate-modified oligolactide polymer network and phosphate invert glasses in the system P2O5-CaO-MgO-Na2O-(TiO2). Porous glasses with an open interconnective porosity were produced by a salt sintering process. Compressive strengths were significantly enhanced by polymer coating of the inner surface of the porous glasses or by fabrication of glass powder-reinforced porous polymer specimens. In vitro degradation in simulated body fluid showed a degradation pattern of the composites which could be modulated by the composition and resulting solubility of the incorporated glass phase. Cytocompatibility of the composites was investigated in a FDA/EtBr viability assay using an MC3T3-E1 osteoblast-like cell line and showed good biocompatibility of the materials in vitro.
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PMID:Fabrication and in vitro characterization of porous biodegradable composites based on phosphate glasses and oligolactide-containing polymer networks. 1701 56

We have developed a new offline chromatographic approach for the selective enrichment of phosphorylated peptides that is directly compatible with subsequent analysis by online nano electrospray ionization tandem mass spectrometry. In this technique, a titanium dioxide (TiO2)-packed pipette tip is used as a phosphopeptide trap that acts as an offline first-dimension separation step in a two-dimensional chromatography system. This is followed by online nano reversed-phase high-performance liquid chromatography. Here, we present suitable methods for enrichment, optimized separately for each step: sample loading, washing and elution from the TiO2-filled tips. To increase the trapping selectivity of the TiO2 column, we used the sodium salt of 1-octanesulfonic acid combined with 2,5-dihydroxybenzoic acid as ion-pairing agents and displacers for acidic peptides. These agents also improve the binding of phosphorylated peptides and block the binding of non-phosphorylated ones. This enrichment procedure takes 30 min, followed by a 100-min HPLC program, including washing and an elution gradient.
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PMID:Titanium dioxide as a chemo-affinity solid phase in offline phosphopeptide chromatography prior to HPLC-MS/MS analysis. 1754 98

Sludge disposal is one of the most costly and environmentally problematic challenges of modern wastewater treatment worldwide. In this study, a new process was developed, which has a significant potential for lower cost of waste disposal, protection of the environment and public health, and yield of economically useful byproducts. Titanium oxide (TiO2), which is the most widely used metal oxide, was produced from the wastewater sludge generated by the flocculation of secondary wastewater with titanium tetrachloride (TiCl4). Detailed analyses were conducted to compare TiCl4, ferric chloride (FeCl3), and aluminum sulfate (Al2(SO4)3) flocculation. Removal of organic matter and different molecular sizes by Ti-salt flocculation was similar to that of the most widely used Fe- and Al-salt flocculation. The mean size of Ti-, Fe-, and Al-salt flocs was 47.5, 42.5, and 16.9 microm, respectively. The decantability of the settled flocs by TiCl4 coagulant was similar to that by FeC13 coagulant and much higher than that of Al2(SO4)3. The photocatalyst from wastewater (PFW) produced by TiCl4 flocculation was characterized by X-ray diffraction, BET surface area, scanning electron microscopy/energy dispersive X-ray, transmission electron microscopy, photocatalytic activity, and X-ray photoelectron spectroscopy. The resulting PFW was found to be superior to commercial TiO2 (P-25) in terms photocatalytic activity and surface area. The PFW as also found to be mainly doped with C and P atoms. The atomic percentage of the PFW was TiO(1.42)C(0.44)P(0.14).
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PMID:Preparation of titanium dioxide (TiO2) from sludge produced by titanium tetrachloride (TiCl4) flocculation of wastewater. 1759 44

The aim of this work is to evaluate and compare the degradation achieved for three non-steroidal anti-inflammatory drugs (NSAIDs) by heterogeneous TiO2 photocatalytic means in aqueous solution at laboratory scale. The selected pharmaceutical compounds were diclofenac (DCF), naproxen (NPX) and ibuprofen (IBP). These compounds were used in their sodium salt chemical form. Previous experiments (adsorption, photolysis and thermodegradation) were developed to evaluate non-catalytic degradation for each NSAID. Photocatalytic experiments were carried out in a Xe-lamp reactor in order to study the influences of different operational conditions (catalyst load, temperature and dissolved oxygen concentration). These results showed that the optimum amount of TiO2, to achieve maximum degradation, of IBP was 1g/L. In contrast, the maximum degradation for DCF or NPX was observed at a TiO2 loading of 0.1g/L. Temperature had a significant effect only for NPX degradation, achieving almost 99% phototransformation. No significant differences were observed for DCF and IBP at 20, 30 and 40 degrees C. Dissolved oxygen concentration was an important parameter to increase the degradation for NPX and IBP. However, it was observed that its rate of mineralization did not increase. Intermediate metabolites were detected in all cases. Hydroxyl metabolites were the most important residual compounds after the photocatalytic treatment of IBP. The inhibition percentage of bioluminescence from Vibro fischeri--as a toxicity parameter--increased during the irradiation time due to the residual concentration of the hydroxyl metabolites generated. However, after 120 min, in experiments with 40 mg/L of dissolved oxygen, a decrease of the % inhibition was observed. Only photocatalytic treatment of IBP drives to a satisfactory biodegradability index BOD5/COD (between 0.16 and 0.42) and, only in this case, a post-biological treatment could be suggested.
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PMID:Photocatalytic degradation of non-steroidal anti-inflammatory drugs with TiO2 and simulated solar irradiation. 1776 Dec 9

The effectiveness of advanced oxidation processes in a batch and a flow reactor was investigated for the remediation of hydrocarbon pollution in the groundwater underlying a petrochemical industrial site. The main organic contaminants present in the groundwater were MTBE, benzene, alkyl-benzenes and alkyl-naphthalenes. Experimental results with a batch reactor showed that for all the organic contaminants the removal efficiency order is UV/TiO2 approximately UV/H2O2>UV (medium-pressure) in a synthetic aqueous solution, compared to UV/H2O2>UV (medium-pressure)>UV/TiO2 for the real polluted groundwater. The much lower performance of UV/TiO2 with respect to UV/H2O2 was inferred to the matrix of the groundwater, i.e. the salt content, as well as the organic and particulate matter. In fact, it is likely that the salts and dissolved organic matter quench the superoxide anion O2(-) and hydroxyl radicals just formed at the surface of the TiO2 catalyst. MTBE was the hardest compound to remove with each of the investigated treatments. UV and UV/TiO2 treatments were not able to reach a residual concentration of 10 microg/L (set by Italian legislation) even after 180 min. As for the UV/H2O2 process, only the MTBE degradation rate resulted affected by the initial H2O2 concentration, while for other compounds a complete removal was obtained within 20 min even with the lowest H2O2 concentration used (0.13 g/L). Only after 120 min of treatment, with an initial H2O2 concentration of 0.13 g/L, did the residual MTBE concentration fall below the above reported maximum admissible concentration. Instead, by using an initial concentration of 2g/L a residual concentration lower than 5 microg/L was obtained after just 30 min of reaction. The UV/H2O2 process was also investigated with a flow reactor. Results showed that it was more efficient than the batch reactor for removing MTBE, in terms of reaction time and initial H2O2 concentration required. This is consistent with the higher power of the UV lamp and with the different geometry of the flow reactor, which has a much shorter optical path than the batch reactor. By-product characterisation was also performed showing that t-butyl-formate and low molecular weight organic acids are formed as intermediate and final by-products, respectively. Finally, a preliminary evaluation of the operational cost of the UV/H2O2 process showed a value of 1.7 euro/m3 under the optimised condition.
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PMID:Effectiveness of UV-based advanced oxidation processes for the remediation of hydrocarbon pollution in the groundwater: a laboratory investigation. 1789 2


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