Abstract  A column leaching experiment was used to investigate the efficacy of amendments on their ability to remove alkaline anions and metal ions from bauxite residue leachates. Treatments included, simulated acid rain (AR), phosphogypsum + vermicompost (PVC), phosphogypsum + vermicompost + simulated acid rain (PVA), and biosolids + microorganisms (BSM) together with controls (CK). Results indicated that amendment could effectively reduce the leachate pH and EC values, neutralize OH-, CO32-, HCO3-, and water soluble alkali, and suppress arsenic (As) content. Correlation analysis revealed significant linear correlations with pH and concentrations of OH-, CO32-, HCO3-, water-soluble alkali, and metal ions. BSM treatment showed optimum results with neutralizing anions (OH-, CO32-, and HCO3-), water soluble alkali, and removal of metal ions (Al, As, B, Mo, V, and Na), which was attributed to neutralization from the generation of small molecular organic acids and organic matter during microbial metabolism. BSM treatment reduced alkaline anions and metal ions based on neutralization reactions in bauxite residue leachate, which reduced the potential pollution effects from leachates on the soil surrounding bauxite residue disposal areas.

Abstract  Herein, novel V-modified titania nanorod-aggregates (VTNA), consisting of fine individual nanorods in radial direction, were fabricated via an efficient microwave-assisted hydrothermal (MWH) route. VTNA with high crystallinity and homogeneous mesopores were obtained by 30 min MWH processing at 190 °C; moreover, a mixed rutile-anatase phase appeared after vanadium doping. XPS analysis revealed that vanadium existed in the forms of V4+ and V5+ on the surface of MWV05 with V5+ being the dominant component, the content of which was approximately 3.5 times that of V4+. Vanadium implanting was achieved efficiently by doping 0.5 and 1 at% V using a rapid MWH process and contributed towards the dramatic improvement of the visible-light response, with E g decreasing from 2.91 to 2.71 and 2.57 eV with the increasing V doping content. MWV05 exhibited optimal photocatalytic degradation activity of water-soluble PCP-Na under solar light irradiation. The enhanced photodecomposition was attributed to the red-shift in the TiO2 band-gap caused by vanadium impregnation, efficient charge separation due to the V4+/V5+ synergistic effects and the free migration of charge carriers along the radial direction of the nanorods arranged in a self-assembled VTNA microstructure.

Abstract  Protonolysis of the titanium alkyl complex [Ti(CH2 SiMe3 )(Xy-N3 N)] (Xy-N3 N=[{(3,5-Me2 C6 H3 )NCH2 CH2 }3 N]3- ) supported by a triamidoamine ligand, with [NEt3 H][B(3,5-Cl2 C6 H3 )4 ] or [PhNMe2 H][B(C6 F5 )4 ] afforded the cations [Ti(Xy-N3 N)][A] (A- =[B(3,5-Cl2 C6 H3 )4 ]- (1[B(ArCl )4 ]; B(ArCl )4 =tetrakis(3,5-dichlorophenyl)borate); A- =[B(C6 F5 )4 ]- (1[B(ArF )4 ]; B(ArF )4 =tetrakis[3,5-bis(trifluoromethyl)phenyl]borate). These Lewis acidic cations were reacted with coordinating solvents to afford the cations [Ti(L)(Xy-N3 N)][B(C6 F5 )4 ] (2-L; L=Et2 O, pyridine and THF). XRD analysis revealed a trigonal monopyramidal (TMP) geometry for the tetracoordinate cations in 1[B(ArX )4 ] and trigonal bipyramidal (TBP) geometry for the pentacoordinate cations in 2-L. Variable-temperature NMR spectroscopy showed a dynamic equilibrium for 2-Et2 O in solution, involving the dissociation of Et2 O. Coordination to the titanium(IV) center activated the THF molecule, which, in the presence of NEt3 , underwent ring-opening to give the titanium alkoxide [Ti(O(CH2 )4 NEt3 )(Xy-N3 N)][B(3,5-Cl2 C6 H3 )4 ] (3). Hydride abstraction from Cβ,eq of the triamidoamine ligand arm in [Ti(CH2 SiMe3 )(Xy-N3 N)] or [Ti(NMe2 )(Xy-N3 N)] with [Ph3 C][B(3,5-Cl2 C6 H3 )4 ] led to the diamidoamine-imine complex [Ti(R){(Xy-N=CHCH2 )(Xy-NCH2 CH2 )2 N}][B(3,5-Cl2 C6 H3 )4 ] (R=CH2 SiMe3 (4 a); R=NMe2 (4 b)). Hydride addition to 4 b with [Li(THF)][HBPh3 ] gave [Ti(NMe2 )(Xy-N3 N)], whereas KH deprotonated further to give [Ti(NMe2 ){(Xy-NCH=CH)(Xy-NCH2 CH2 )2 N}] (5). XRD on single crystals of 3 and 4 b confirmed the proposed structures.