Biofibers. natural lignocellulosics, have an outstanding potential a s a reinforcement in thermoplastics. This study deals with the preparation of lignocellulosic composites by reactive extrusion processing in which good interfacial adhesion is generated by a combination of fiber modification and matrix modification methods. PP matrix was modified by reacting with maleic anhydride and subsequently bonded to the surface of the modified lignocellulosic component, in-situ. The fiber surface was modified by reacting it with a silane in a simple and quick aqueous reaction system, similar to that employed for glass fibers. The modified fibers are then extruded with the modified polymer matrix to form the compatibilized composite. The various reactions between the lignocellulosic fiber/filler and modified polymer chains, is expected to improve the interfacial adhesion significantly a s opposed to simple mixing of the two components, since new covalent bonds between the fiber surface and matrix are created in the former case. These composite blends were then injection molded for mechanical characterization. Typical mechanical tests on strength, toughness and Izod impact energy were performed and the results are reported. These findings are discussed in view of the improved adhesion resulting from reactions and enhanced polar interactions at phase boundaries.

There are increasing requirements worldwide for advanced separation materials with applications in environmental protection processes. Various mesoporous polymeric materials have been developed and they are considered as potential candidates. It is still challenging, however, to develop economically viable and durable separation materials from low-cost, mass-produced materials. Here we report the fabrication of a nanofibrous network structure from common polymers, based on a microphase separation technique from frozen polymer solutions. The resulting polymer nanofibre networks exhibit large free surface areas, exceeding 300 m2 g−1, as well as small pore radii as low as 1.9 nm. These mesoporous polymer materials are able to rapidly adsorb and desorb a large amount of carbon dioxide and are also capable of condensing organic vapours. Furthermore, the nanofibres made of engineering plastics with high glass transition temperatures over 200 °C exhibit surprisingly high, temperature-dependent adsorption of organic solvents from aqueous solution.

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Lithium-ion capacitors (LICs) represent a new type of energy-storage devices, which have combined merits of high energy density Li-ion battery and high power density supercapacitor. Nevertheless, one significant challenge for LICs is the imbalanced kinetics between the fast capacitive cathode and relatively slow intercalation anode that limit the energy-storage performance. Here, the asymmetric LIC devices were developed based on a nitrogen-doped, carbonized zeolitic imidazolate framework (ZIF-8) cathode and a three-dimensional, nano-network-structured, conversion reaction-based Ni/NiO/C anode. These nanostructures associated with both the cathode and anode enable rapid electron and ions transport in the LIC devices, which allows the asymmetric LICs to be operated on either high energy mode (energy density of 114.7 Wh/kg at power density of 98.0 W/kg) or high power mode (power density of 60.1 kW/kg at energy density of 17.6 Wh/kg). The device also exhibited long-term cycle stability with 87% capacitance retention after 12 000 cycles. These results demonstrate that the rational design of nanoporous electrode structures can deliver a balanced, high-performance-activated cZIF-8|Ni/NiO/C-based lithium-ion capacitor.