ABSTRACT
Titanium silicon molecular zeolite (TS-1) plays an important role in catalytic reactions due to its unique nanostructure. The straight channel on TS-1 was parallel to the orientation of the short b-axis and directly exposed to the aperture of the 10-member ring with a diameter of 0.54 nm × 0.56 nm. This structure could effectively reduce the diffuse restriction of bulk organic compounds during the oxidative desulfurization process. As a kind of cationic polymer electrolyte, polydimethyldiallyl ammonium chloride (PDDA) contains continuous [C8H16N+Cl-] chain segments, in which the Cl- could function as an effective structure-directing agent in the synthesis of nanomaterials. The chain of PDDA could adequately interact with the [0 1 0] plane in the preparation process of zeolite, and then the TS-1 nanosheet with short b-axis thickness (6 nm) could be obtained. The pore structure of the TS-1 nanosheet is controlled by regulating the content of PDDA. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), N2 physical adsorption analysis, infrared absorption spectrum and ultraviolet-visible spectrum were used to determine the TS-1. The thinner nanosheets exhibit excellent catalytic performance in oxidative desulfurization of dibenzothiophene (DBT), in which the removal rate could remain at 100% after three recycles. Here, the TS-1 nanosheet with short b-axis thickness has a promising future in catalytic reactions.
ABSTRACT
Hydrothermal synthesis is a typical method for the preparation of TS-1. In the current study, agitation was introduced during the crystallisation stage, and nano-sized TS-1 with little anatase TiO2 was successfully synthesised in a short time (1-8 h). Furthermore, under rotational crystallisation conditions, a series of TS-1 samples was prepared with different crystallisation times, and the products obtained were investigated as catalysts for the oxidative desulfurisation of thiophene from a model fuel. All samples were characterised utilising X-ray diffraction (XRD), scanning electron microscopy (SEM), N2-adsorption, ultraviolet-visible (UV-Vis) spectroscopy and Fourier-transform infrared (FT-IR) spectroscopy techniques. It was found that under rotational crystallisation conditions, nano-sized TS-1 could be synthesised in a short time that had improved efficiency for the oxidative desulfurisation reaction of thiophene in comparison with TS-1 synthesised by static crystallisation for 24 h.
ABSTRACT
A novel amorphous FeOOH modified BiVO4 photocatalyst (A-FeOOH/BiVO4) was successfully produced and characterized by various techniques. The results showed that amorphous FeOOH with about 2 nm thickness evenly covered on BiVO4 surface, which caused resultant A-FeOOH/BiVO4 exhibiting higher visible light photocatalytic performance for producing O2 from water than BiVO4. When the covered amount of amorphous FeOOH was 8%, the resultant photocatalyst possessed the best photocatalytic performance. To find the reasons for the improvement of photocatalytic property, electrochemical experiments, DRS, PL and BET, were also measured, the experimental results indicated that interface effect between amorphous FeOOH and BiVO4 could conduce to migration of photogenerated charge, and exhibit stronger light responded capacity. These positive factors promoted A-FeOOH/BiVO4 presenting improved the photocatalytic performance. In a word, the combination of amorphous FeOOH with BiVO4 is an effective strategy to conquer important challenges in photocatalysis field.
