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21.
《Ceramics International》2022,48(15):21988-21995
Bi4O5Br2/MnxZn1-xFe2O4 nanocomposites with impressive photocatalytic and recyclability properties were synthesised using a microemulsion method. In addition to the photocatalytic effect, the crystal structure and morphology, photoelectrochemical characteristics, magnetic effect and photocatalytic mechanism of Bi4O5Br2/MnxZn1-xFe2O4 were also investigated. As the best sample, the removal rate of the Bi4O5Br2/MnxZn1-xFe2O4 photocatalyst with 7.5 wt% MnxZn1-xFe2O4 to rhodamine B (RhB) reached up to 99.4% within 60 min. The enhanced photocatalyst activity was mainly attributed to the type-II heterojunction formed between Bi4O5Br2 and MnxZn1-xFe2O4, which not only optimised the energy band structure, but also led to the building of an interior electromagnetic field within the Bi4O5Br2/MnxZn1-xFe2O4 heterojunction. Meanwhile, the constantly producing and migrating h+ and ·O2? were the main active components. In particular, the results of the saturation magnetization tests and magnetic recovery experiments revealed that the magnetic composite photocatalyst can be recovered effectively. The results of the removal rate of RhB remaining at 85.2% after five uses reflected the advantages of the stability of the Bi4O5Br2/MnxZn1-xFe2O4 photocatalyst. In brief, this paper presented an original idea to develop a novel composite magnetic photocatalyst and research the enhancement mechanism of photocatalysis. 相似文献
22.
《International Journal of Hydrogen Energy》2022,47(10):6755-6766
Mg-based hydride is a promising hydrogen storage material, but its capacity is hindered by the kinetic properties. In this study, Mg–Mg2Ni–LaHx nanocomposite is formed from the H-induced decomposition of Mg98Ni1·67La0.33 alloy. The hydrogen capacity of 7.19 wt % is reached at 325 °C under 3 MPa H2, attributed to the ultrahigh hydrogenation capacity in Stage I. The hydrogen capacity of 5.59 wt % is achieved at 175 °C under 1 MPa H2. The apparent activation energies for hydrogen absorption and desorption are calculated as 57.99 and 107.26 kJ/mol, which are owing to the modified microstructure with LaHx and Mg2Ni nanophases embedding in eutectic, and tubular nanostructure adjacent to eutectic. The LaH2.49 nanophase can catalyze H2 molecules to dissociate and H atoms to permeate due to its stronger affinity with H atoms. The interfaces of these nanophases provide preferential nucleation sites and alleviate the “blocking effect” together with tubular nanostructure by providing H atoms diffusion paths after the impingement of MgH2 colonies. Therefore, the superior hydrogenation properties are achieved because of the rapid absorption process of Stage I. The efficient synthesis of nano-catalysts and corresponding mechanisms for improving hydrogen storage properties have important reference to related researches. 相似文献
23.
《Ceramics International》2021,47(22):31713-31723
Continuous carbon-fibre-reinforced Cs-geopolymer composite (Cf/CsGP) were prepared, and its in-situ conversion was investigated during high-temperature treatments. The effect of treatment temperature on the thermal evolution process and mechanical properties of the resulting products were systematically evaluated. The results indicated that the crystallization temperature of Cf/CsGP composite was considerably delayed because the amorphous structure of carbon fibres was not conducive as a nucleation substrate for pollucite derived from the CsGP matrix. Moreover, the integrity of the corresponding resulting products derived from the Cf/CsGP composite were damaged due to thermal shrinkage that occurred during the high-temperature treatment process. When treatment temperature was ≤1200oC, the mechanical properties of the corresponding products exhibited an upward trend, which was ascribed to the improvement of the densification degree of the resulting composite and well interface-bonding state between carbon fibres and pollucite. However, the mechanical properties of the resulting composites decreased with the treatment temperature continued increased from 1200 to 1400oC. This phenomenon was attributed to the impairment of fibre properties caused by interfacial reactions. 相似文献
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Xiaojin Li Quanxin Yang Hongliang Liu Yingying Ren Xuping Wang Pengfei Wu 《Ceramics International》2021,47(9):11989-11992
We observe enhancements of both conductive and dielectric properties under UV illumination by using a ferroelectric absorber, potassium tantalate niobate (KTa1-xNbxO3, KTN). The UV-generated electron-hole pairs weaken the intrinsic ferroelectric polarization while enhance the conductive property. The UV-induced heat effect causes the enhancement of the dielectric property. The results are further confirmed by the maximal rectification ratio which shows an opposite trend between the direct heating process and the UV illumination. Our results are useful for better understanding of ferroelectric properties under UV illumination and the development of new optoelectronic devices. 相似文献
27.
综述了近几年国内外改性聚乳酸(PLA)发泡技术的研究进展,针对PLA在发泡方面熔体强度和结晶性能的不足,介绍了通过加入扩链剂、交联剂、成核剂、纤维和其他聚合物等物质来改善PLA发泡性能的方法、效果和机理;最后,对改性聚乳酸发泡技术的未来发展进行了展望。 相似文献
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To improve the hydrophobicity of bagasse hemicellulose-based films, glutaraldehyde was applied when preparing films of original and cationic bagasse hemicellulose with the addition of polyvinyl alcohol and sorbitol. The results showed that the cationic modification could increase the hydrophobicity of the hemicellulose-based film, and the hydrophobicity of hemicellulose-based films crosslinked with glutaraldehyde also increased. However, cationic modification of hemicellulose decreased the stress of the hemicellulose-based film. While crosslinking with glutaraldehyde increased the stress of both the original and cationic hemicellulose-based films. Macrophotography indicated that the film formability of the original hemicellulose was better than that of cationic hemicellulose. Through SEM observation, the degree of bonding of different components of the films was found to be increased due to crosslinking with glutaraldehyde. The crosslinking reaction between glutaraldehyde and hemicellulose was further confirmed by FT-IR spectroscopy. 相似文献
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