Photocatalytic Degradation of 4,4′-Isopropylidenebis(2,6-Dibromophenol) on Sulfur-Doped Nano TiO2

In present work, we examine the photocatalytic properties of S-doped TiO2 (S1, S2) compared to bare TiO2 (S0) in present work. The photocatalytic tests were performed in alkaline aqueous solutions (pH = 10) of three differently substituted phenols (phenol (I), 4,4′-isopropylidenebisphenol (II), and 4,4′-isopropylidenebis(2,6-dibromophenol) (III)). The activity of the catalysts was evaluated by monitoring I, II, III degradation in the reaction mixture. The physicochemical properties (particle size, ζ-potential, Ebg, Eu, E0cb, E0vb, σo, KL) of the catalysts were established, and we demonstrated their influence on degradation reaction kinetics. Substrate degradation rates are consistent with first-order kinetics. The apparent conversion constants of the tested compounds (kapp) in all cases reveal the sulfur-loaded catalyst S2 to show the best photocatalytic activity (for compound I and II S1 and S2 are similarly effective). The different efficiency of photocatalytic degradation I, II and III can be explained by the interactions between the catalyst and the substrate solution. The presence of bromine substituents in the benzene ring additionally allows reduction reactions. The yield of bromide ion release in the degradation reaction III corresponds to the Langmuir constant. The mixed oxidation-reduction degradation mechanism results in higher degradation efficiency. In general, the presence of sulfur atoms in the catalyst network improves the degradation efficiency, but too much sulfur is not desired for the reduction pathway.

Application of Ferrites as Electrodes for Supercapacitor

Apart from the magnetic properties, ferrites have been considered as efficient electrodes for next generation energy storage devices. This chapter will include applications of spinel ferrites such as MnFe2O4, CoFe2O4, ZnFe2O4 and NiFe2O4 in supercapacitor. In ferrites, the charge storage arises from the fast-reversible surface redox reactions at the electrode/electrolyte interface. In particular, the electrode material with high specific capacitance, wide range of operating potential, low synthesis cost and its availability on the earth are highly desirable to fabricate a supercapacitor. Ferrites with mixed oxidation states have proved as promising electrodes in supercapacitors. In this chapter, we summarize the different synthesis methods of ferrites based nanocomposites and their electrochemical properties for supercapacitor application.

Seeded Growth of Au@CuxO Core–Shell Mesoporous Nanospheres and Their Photocatalytic Properties

We report a facile synthesis of Au@CuxO core–shell mesoporous nanospheres with tunable size in the aqueous phase via seeded growth. The success of the current work relies on the use of a halide-free copper (Cu) precursor and n-oleyl-1,3-propanediamine as a capping agent to facilitate the formation of a copperish oxide shell with a mesoporous structure and the presence of mixed oxidation states of Cu. By varying the amount of spherical Au seeds while keeping other parameters unchanged, their diameters could be readily tuned without noticeable change in morphology. As compared with commercial Cu2O, the as-prepared Au@CuxO core–shell mesoporous nanospheres exhibit the higher adsorption ability, enhanced activity, and excellent stability toward photocatalytic degradation of methyl orange (MO) under visible light irradiation, indicating their potential applications in water treatment.

The Selective Oxidation of Cyclohexane via In-situ H2O2 Production Over Supported Pd-based Catalysts

The oxidation of cyclohexane via the in-situ production of H2O2 from molecular H2 and O2 offers an attractive route to the current industrial means of producing cyclohexanone and cyclohexanol (KA oil), key materials in the production of Nylon. The in-situ route has the potential to overcome the significant economic and environmental concerns associated with the use of commercial H2O2, while also allowing for the use of far lower reaction temperatures than those typical of the purely aerobic route to KA oil. Herein we demonstrate the efficacy of a series of bi-functional Pd-based catalysts, which offer appreciable concentrations of KA oil, under conditions where limited activity is observed using O2 alone. In particular the introduction of V into a supported Pd catalyst is seen to improve KA oil concentration by an order of magnitude, compared to the Pd-only analogue. In particular we ascribe this improvement in catalytic performance to the development of Pd domains of mixed oxidation state upon V incorporation as evidenced through X-ray photoelectron spectroscopy. Graphic Abstract

Self-assembly of a trigonal bipyramidal architecture with stabilisation of iron in three spin states

Self-assembly of a trigonal bipyramidal architecture with a central mixed oxidation state star from a heterotopic ligand and a single metal salt. Characterisation confirms incorporation of iron as low-spin iron(ii), high-spin iron(ii) and iron(iii).