Performance Analysis of Plant Shells/PVC Composites under Corrosion and Aging Conditions

To make full use of plant shellfibers(rice husk,walnut shell,chestnut shell),three kinds of wood-plastic com-posites of plant shellfibers and polyvinyl chloride(PVC)were prepared.X-ray diffraction analysis was carried out on three kinds of plant shellfibers to test their crystallinity.The aging process of the composites was conducted under 2 different conditions.One was artificial seawater immersion and xenon lamp irradiation,and the other one was deionized water spray and xenon lamp irradiation.The mechanical properties(tensile strength,flexural strength,impact strength),changes in color,water absorption,Fourier transform infrared spectroscopy(FTIR),and microstructures of the composites before and after the two aging experiments were analyzed.The results showed that the chestnut shell had the highest crystallinity,which was 42%.The chestnut shell/PVC composites had the strongest interface bonding,the least internal defects,and the best general mechanical properties among the three composites.Its tensile strength,bending strength and impact strength were 23.81 MPa,34.12 MPa,and 4.32 KJ·m^(-2),respectively.Comparing the two aging conditions,artificial seawater immersion and xenon lamp irradiation destroyed the quality of the combination of plant shellfibers and PVC,making the internal defects of the composites increase.This made the water absorption ability and changes in the color of the composites more obvious and led to a great decrease in the mechanical properties.The general mechanical properties of the chestnut shell/PVC composites were the best,but their water absorption ability changed more obviously.

Effect of Carbonation and Drying-Wetting Cycles on Chloride Diffusion Behavior of Coral Aggregate Seawater Concrete

Based on seawater immersion,drying-wetting cycles,carbonation and drying-wetting cycles for coral aggregate sea-water concrete(CASC)with different strength grades,the effect of carbonation and drying-wetting cycles on chloride diffusion be-havior of CASC is studied.The results show that the free surface chloride concentration(Cs),free chloride diffusion coefficient(Df)and time-dependent index(m)of CASC in the drying-wetting cycles is obviously higher than that in seawater immersion.The Df and m of CASC of carbonation and drying-wetting cycles is higher than that in the drying-wetting cycles.Carbonation increases the Df and m of CASC,which is against CASC to resist chloride corrosion.The corrosion possibility of CASC structures in different ex-posed areas is as follows:splash zone(carbonation and drying-wetting cycles)>tidal zone(drying-wetting cycles)>underwater zone(seawater immersion).Besides,the chloride diffusion rate of C65-CASC is 17.8%-63.4%higher than that of C65-ordinary aggre-gate concrete(OAC)in seawater immersion(underwater zone).Therefore,anti-corrosion measures should be adopted to improve the service life of CASC structure in the oceanic environment.

An Approach to Determination of Phenolic Compounds in Seawater using SPME-GC-MS Based on SWCNTs Coating

Phenolic compounds have become one kind of the important pollutants of the marine environment. Single-walled Carbon nanotubes, as one-dimensional nano materials, have light weight and perfect hexagonal structure of connections, with many unusual mechanical, chemical and electrical properties. In recent years, with the research of carbon nanotubes and other nano materials, the application prospect is also constantly discussed. In this paper, homemade single-walled carbon nanotubes(SWCNTs) coating was used for establishing an analytical approach to the determination of five kinds of phenolic compounds in seawater using SPME-GC-MS. Optimal conditions: After saturation was conducted with Na Cl, and p H was adjusted to 2.0 with H_2SO_4, the extract was immersed in a water bath at 40 for GC℃-MS determination through 40-min agitating extraction at 500 rmin^(-1) and 3-min desorption at 280℃. The liniearities ranged between 0.01-100 μg L^(-1), and the determination limits ranged between 1.5-10 ngL^(-1). The relative standard deviation(RSD, n = 5) was less than 6.5%. For the phenolic compounds obtained from the spiked recovery test for actual seawater samples, the rates of recovery were 87.5%-101.7%, and the RSDs were less than 8.8%, which met the requirements of determination. Due to its simplicity, high efficiency and low consumption, this approach is suitable for the analysis of trace amounts of phenolic compounds in marine waters.

Evolution of the Corrosion Product Film and Its Effect on the Erosion–Corrosion Behavior of Two Commercial 90Cu–10Ni Tubes in Seawater

The composition and structural evolution of the corrosion product film of two commercial 90Cu-10Ni tubes, namely TubeA and Tube B, after being immersed in natural seawater for 1, 3, and 6 months were characterized by scanning electronmicroscopy, energy-dispersive X-ray spectroscopy, X-ray diffraction, and X-ray photoelectron spectroscopy, and its effecton the erosion--corrosion behavior of the tubes was determined through a rotating cylinder electrode system using variouselectrochemical techniques. For the freshly polished samples used as contrast samples, the flow velocity mainly enhancedthe cathodic reaction at low flow velocities while both the anodic and the cathodic reactions were remarkably accelerated athigher flow velocities. The corrosion product films formed on the two commercial 90Cu-10Ni tubes after being immersedin seawater for up to 6 months are of a complex three-layer or multilayer structure. The structural evolution of the films isout of sync for the two tubes. A continuous residual substrate layer depleted of Ni was observed in the inner layer of thefilms on Tube B after 30, 90, and 180 days＇ immersion, while it was observed in the film on Tube A only after 180 days＇immersion. The nature of the inner layer plays a crucial role in the erosion-corrosion resistance of the 90Cu-10Ni tubes athigher flow velocity. The film with a compact and continuous inner layer of Cu20 doped with Ni2＋ and Ni3＋ which bondsfirmly with the substrate could survive and even get repaired with the increased flow velocity. The film on Tube Bpossessing a hollow and discontinuous inner layer composed of the residual substrate was degraded rapidly with increasingrotation speed in spite of its quite good resistance at the stagnant or lower speed conditions.