Order of magnitude increase in photocatalytic rate for hierarchically porous anatase thin films synthesized from zinc titanate coatings

In this paper we report on the use of aerosol assisted chemical vapour deposition (AACVD) to form thin films of the zinc titanate phases using zinc acetate and titanium isopropoxide as precursors in methanol solution. Analysis by XRD and XPS found that through variation in experimental conditions we have been able to synthesize films of zinc titanate with composition of Zn2TiO4 or Zn0.3Ti2.7O4.94, which adopt the spinel and pseudobrookite structure respectively. In addition, we have also formed hybrid films of Zn2TiO4 with either ZnTiO3 or ZnO. Using a technique previously reported with powders, the mixed ZnO and Zn2TiO4 films were treated with acid to produce porous Zn2TiO4 which, through reduction and vapour leaching of zinc, were converted to hierarchically porous thin films of anatase TiO2. This conversion was monitored by XRD. Analysis of photocatalytic activity of the hierarchically porous titania, using dye and stearic acid degradation tests, found a factor of 12 to 14 increase in rates of photocatalysis over conventional TiO2 thin films. Finally we are able to report a maximum formal quantum efficiency for stearic acid degradation of 1.76 × 10−3 molecules per photon

Synthesis and characterisation of single-source CVD precursors for M-N-Si composites

EThOS - Electronic Theses Online ServiceGBUnited Kingdo

1,8-Bis(silylamido)naphthalene complexes of magnesium and zinc synthesized through alkane elimination reactions

The reactions between magnesium or zinc alkyls and 1,8-bis(triorganosilyl)diaminonaphthalenes afford the 1,8-bis(triorganosilyl)diamidonaphthalene complexes with elimination of alkanes. The reaction between 1,8-C10H6(NSiMePh2H)2 and one or two equivalents of MgnBu2 affords two complexes with differing coordination environments for the magnesium; the reaction between 1,8-C10H6(NSiMePh2H)2 and MgnBu2 in a 1:1 ratio affords 1,8-C10H6(NSiMePh2)2{Mg(THF)2} (1), which features a single magnesium centre bridging both ligand nitrogen donors, whilst treatment of 1,8-C10H6(NSiR3H)2 (R3 = MePh2, iPr3) with two equivalents of MgnBu2 affords the bimetallic complexes 1,8-C10H6(NSiR3)2{nBuMg(THF)}2 (R3 = MePh2 2, R3 = iPr3 3), which feature four-membered Mg2N2 rings. Similarly, 1,8-C10H6(NSiiPr3)2{MeMg(THF)}2 (4) and 1,8-C10H6(NSiMePh2)2{ZnMe}2 (5) are formed through reactions with the proligands and two equivalents of MMe2 (M = Mg, Zn). The reaction between 1,8-C10H6(NSiMePh2H)2 and two equivalents of MeMgX affords the bimetallic complexes 1,8-C10H6(NSiMePh2)2(XMgOEt2)2 (X = Br 6; X = I 7). Very small amounts of [1,8-C10H6(NSiMePh2)2{IMg(OEt2)}]2 (8), formed through the coupling of two diamidonaphthalene ligands at the 4-position with concomitant dearomatisation of one of the naphthyl arene rings, were also isolated from a solution of 7

Phosphorus-substituted azulenes accessed via direct hafner reaction of a phosphino cyclopentadienide

The Hafner azulene synthesis may be applied to the direct synthesis of phosphorus-substituted azulenes, when a phosphinocyclopentadienide is used as one of the reactants. The azulenyl phosphines produced in this fashion are preferentially isolated as the corresponding phosphine oxides or phosphine borane adducts.</p

Validation of the NG-18 equations for thick walled pipelines

The applicability of the flow stress dependent NG-18 equations to thick wall pipelines such as those used to transport dense phase carbon dioxide (CO2) is demonstrated. A comparison between the components of the NG-18 equations and BS 7910 shows that the factor MT for though-wall defects and MP for part-wall defects in the NG-18 equations are very close to the reference stress solutions in BS 7910 Annex P, which are applicable to thick wall pipe. Thus, by inference, the flow stress dependent form of the NG-18 equations is also applicable to thick wall pipe. A further comparison with experimental failure data for thick wall pipes shows that the flow stress dependent NG-18 equations are applicable to wall thicknesses of up to 47.2 mm when the full-size equivalent upper shelf Charpy V-notch impact energy is at least 50 J. The results suggest that in principle, the flow stress dependent NG-18 equations may be used as limit state functions in models to calculate the failure frequency due to third party external interference, for high toughness, thick wall pipelines such as those required for dense phase CO2 pipelines

Can Limit State Design be used to Design a Pipeline Above 80% SMYS?’, OMAE

ABSTRACT This paper contains the results of a preliminary study, undertaken by C-FER and Andrew Palmer and Associates, for BP Exploration, to demonstrate the feasibility of utilizing limit states design procedures for the design of large diameter, onshore pipelines in remote areas. The objective of the study was to determine if a higher design factor can be justified than that currently specified for such a region; specifically if an increase in the basic design factor, F, from approximately 0.72 to 0.85 could be justified, thereby allowing the pipeline wall thickness to be reduced and a substantial weight saving to be achieved. The work included reliability analyses for three limit state failure scenarios: burst of undamaged pipelines, burst of corroded pipelines and burst of pipelines containing dents and gouges. Results presented show: (1) the calculated probability of rupture for a new pipe (i.e., with no damage, corrosion or other forms of deterioration); (2) the probabilities of failure for pipes containing corrosion or dent/gouge defects; and (3) the effects of a higher design pressure for each limit states scenario. The paper discusses the results, comments on the feasibility of justifying higher design factors and discusses the importance of an appropriate pipeline maintenance management system for monitoring and controlling structural integrity for the full life of a pipeline

Synthesis and materials chemistry of bismuth <em>Tris</em>-(di-i-propylcarbamate):deposition of photoactive Bi₂O₃ thin films

δ- and β-Bi2O3 thin films can be deposited by AACVD from a Bi(O2CNPri2)3 precursor, with temperature and temporal control over the deposition process. Thin δ-Bi2O3 films show good catalytic activity toward the photodegradation of methylene blue, while β-Bi2O3 nanowires are less active because of an increased hydrophobicity. Controlled hydrolysis of Bi(O2CNPri2)3 affords the novel oxo-cluster Bi8(O)6(O2CNPri2)12

Synthesis and characterization of fluorinated β-ketoiminate zinc precursors and their utility in the AP-MOCVD growth of ZnO:F

A novel family of zinc bis beta-ketoiminate complexes 2b-2h have been synthesized by reaction of the isolated free ligands (1a-h) with dimethylzinc. The isolated zinc complexes were characterized by elemental analysis, NMR spectroscopy, and in the case of 2b-d and 2f-h, the molecular structures of the complexes were determined by single crystal X-ray diffraction which reveals the compounds to be pseudo-octahedral 6-coordinate, monomeric homoleptic complexes in the solid state. TG analysis showed complexes 2b-f all to have residual masses at 400 °C of 10% or less, well below the value for ZnO and thus indicative of volatility. Of these systems 2b [Zn{MeC(O)CHC(NCH2CH2OMe)CF3}2] has been investigated for its utility in the AP-MOCVD growth of F –doped ZnO (ZnO:F) in the absence of additional oxidant at 400 °C on glass and silicon substrates