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A strong solid/liquid interfacial interaction is found between porous alumina and graphene oxide (GO) aqueous dispersion, which promotes a fast enrichment of GO on the alumina surface and results in the formation of a GO hydrogel. [ABSTRACT FROM AUTHOR]

Metal coatings with good conductivity and hydrophobicity property were prepared on wood surface via a simple electroless nickel (Ni) approach. The variation of crosssectional area for coatings on wood surface was investigated. The cross-sectional area of the coatings increased as the number of deposition steps was increased. The resistance, conductivity, and hydrophobicity property of the coatings were obviously enhanced with the increase in the number of depositions. The composite structure was characterised with scanning electron microscopy (SEM) images. The conductivity and hydrophobicity property of the ideal coatings on wood surface can be greatly improved. Here, the resistance of longitudinal coatings was as large as 28.4 mΩ and the conductivity can be up to 706.7 S/cm. The resistance of the coatings was decreased 5 times compared with that of coatings obtained via a single deposition. The contact angle of coatings varied in angle between 90.7 and 116.89°. The cross-sectional area change of coatings had a direct influence on the properties of coatings. [ABSTRACT FROM AUTHOR]

Hollow composite coatings were prepared on the surface of cellulose fibres by a simple electroless Ni-P/nano-SiC approach. The metal coated extent, dispersion extent of micro/nano cellulose fibres and crystalline structure of Ni-P/nano-SiC composite coatings were investigated. The homogeneous hollow composite coatings and metal coated extent of micro/nano cellulose fibres were improved with increase in concentration of nano-SiC in the coatings, and the ideal composite coatings were obtained within the range of 0.2 to 0.35 g (0.6 g/l) nano-SiC in the solution bath. The metallisation for cellulose fibres enhanced the dispersion extent of micro-nano cellulose fibres. A uniform coating, consisting of the hollow coating on cellulose fibres surface, could be obtained. At the same time, metallisation did not damage the original structure and surface functional groups of the cellulose fibres. The concentration of nano-SiC, ultrasonic time, ultrasonic power and cellulose concentration had a direct influence on the metal coated extent on the surface of cellulose fibres. The coated extent, dispersion extent and crystalline structure of metallisation cellulose fibres would exhibit ideal characteristics. Here, the concentration of cellulose fibres, ultrasonic time, ultrasonic power and the concentration of nano-SiC were 1.2 g/l, 120 min, 960 W and 0.6 g/l, respectively. [ABSTRACT FROM AUTHOR]