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In this work, a series of bio-based, biodegradable and amorphous shape memory polyurethanes were synthesized by a two-step pre-polymerization process from polylactide (PLA) diol, polycaprolactone (PCL) diol and diphenylmethane diisocyanate-50 (MDI-50). The ratio of PLA diol to PCL diol was adjusted to investigate their thermal and mechanical properties. These bio-based shape memory polyurethanes (bio-PUs) showed a glass transition temperature (Tg) value in the range of −10.7–32.5 °C, which can be adjusted to be close to body temperature. The tensile strength and elongation of the bio-PUs could be tuned in the range from 1.7 MPa to 12.9 MPa and from 767.5% to 1345.7%, respectively. Through a series of shape memory tests, these bio-PUs exhibited good shape memory behavior at body temperature. Among them, PU with 2 : 1 as the PLA/PCL ratio showed the best shape recovery behavior with a shape recovery rate higher than 98% and could fully reach the original shape state in 15 s at 37 °C. Therefore, these shape memory bio-PUs are promising for applications in smart biomedical devices.

Herein, we report the synthesis of a novel hydroxyl epoxy phosphate monomer (PGHEP) as an efficient dispersant for graphene to enhance the compatibility of the graphene in epoxy resin. Raman spectroscopy, Ultraviolet–visible spectroscopy (UV–vis) and X-ray photoelectron spectroscopy (XPS) studies were confirmed the π-π interactions between PGHEP and graphene. Well-dispersed states of PGHEP functionalized graphene (G) sheets in water were analyzed by transmission electron microscopy (TEM), atomic force microscopy (AFM) and scanning electron microscopy (SEM). Further, microstructure of prepared G/waterborne epoxy coatings containing 0.5–1.0 wt.% of PGHEP functionalized G sheets were also observed with the help of SEM and TEM. The PGHEP functionalized G sheets dispersed composite coatings displayed enhanced corrosion resistance compared with pure epoxy resin, these coatings have higher contact angle, lower water absorption as evident from the results of electrochemical impedance spectroscopy (EIS) and salt spray tests. The superior corrosion protection performances of G/epoxy coatings were mainly attributed to the formed passive film from uniformly dispersed PGHEP functionalized G sheets which act as physical barrier on the steel surface. Therefore, this work provides a novel bio-based efficient dispersant for G sheets and an important method for preparing G/waterborne epoxy coatings with superior corrosion resistance properties.

Graphene nanosheets (GNSs) possess outstanding conductivity, good thermal and chemical stabilities and desirable mechanical strengths. However, the unfunctionalized GNSs are hydrophobic and insoluble in water, which limits their application in many technological areas. Herein, we report a design strategy to exfoliate few-layered aqueous dispersible graphene by a simple ball-milling technique. The modifier of sodium lignosulfonate (LS) enables to synthesize LS-decorated GNSs from natural graphite based on the strong π–π interaction, greatly improving GNSs dispersion in water. The resultant GNSs exhibit a high production yield (∼100%), high dispersion concentration and excellent film formation ability. The electrical and thermal conductivities of the as-prepared graphene paper were up to 2385 S cm−1 and 1324 W m−1 K−1, respectively, superior to those of most previously reported graphene materials. This graphene paper with the superb electrical and thermal conduction properties also exhibits excellent mechanical flexibility and structure intensity during bending, which has potential usages in electronic packaging and high power thermal management.

Correction for ‘An ultrahigh thermal conductive graphene flexible paper’ by Jiheng Ding et al., Nanoscale, 2017, 9, 16871–16878, DOI: 10.1039/C7NR06667H.

A nanoporous organic polymer based on triphenylamine was synthesized, and the structure and morphology of the resultant polytriphenylamine (PTPA) were described by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and N 2 adsorption/desorption analysis. PTPA was acted as the host to load the guest Fe(NO 3 ) 3 for preparing humidity sensitive composites. Compared with pure PTPA sensor, Fe(NO 3 ) 3 /PTPA sensors showed improved humidity sensitive properties, especially the 20 wt% Fe(NO 3 ) 3 /PTPA sensor. The impedance of the 20 wt% Fe(NO 3 ) 3 /PTPA sensor changed four orders of magnitude over the whole humidity range, with a good linearity, litter hysteresis, rapid response and good long-time stability. The complex impedance plots and direct current (DC) reverse polarity method were used to research the mechanism of the optimized sensor.

Based on their unique material properties, two-dimensional (2D) nanomaterials such as graphene, molybdenum disulfide (MoS2), and boron nitride (BN) have been attracting increased research interest. The potential of 2D materials, in the form of nanoplatelets that are used as new materials, will be important to both nanomaterials and advanced materials. Water is usually considered to be the ideal dispersed medium, and the essential hydrophobicity and limitations to mass production of 2D nanoplatelets have become quite serious obstacles to their usage in various fields. In this paper, pulping black liquor was used as dispersant, with high concentration of lignin to get single- and few-layered nanoplatelets. The whole process required only the high-shear mixing of 2D layered materials and pulping waste liquor. This method was not only simple and efficient but also environmentally friendly and resource-recycling. Moreover, the fabricated single- or few-layered nanoplatelets possessed good solubility in aqueous solution due to their edge functionalization, and could be well dispersed in water at concentrations (10 mg ml-1 for graphene, 6.3 mg ml-1 for MoS2, and 6.0 mg ml-1 for BN) which were much higher than that of other methods. The dispersions of graphene, MoS2, and BN nanosheets were highly stable over several months, which allowed us to easily prepare graphene, MoS2, and BN films through simple vacuum filtration or spraying. These results indicated that pulping black liquor can be used as a material or reagent, and the mass production of 2D material is possible in a simple and fast method.

In2O3 micro/nanotubes (MNTs) with different diameters are successfully synthesized by an effective and template-free coaxial electrospinning method. The diameters of the MNTs can be simply tailored by controlling the ratio of reactants. The HCHO sensing tests of as-prepared MNTs reveal that the samples possess high response value, fast response and recovery rate, and favorable selectivity. Moreover, compared with the large diameter (∼1 μm or ∼500 nm) In2O3 MNTs, the small diameter (∼100 nm) In2O3 MNTs exhibit highly enhanced sensing properties. The gas sensing mechanism of In2O3 MNTs has been discussed in detail. The promising HCHO-sensing properties enable In2O3 MNTs to be a competitive candidate for detecting poisonous HCHO in practice. The experiment also indicates that the coaxial electrospinning is an environmental friendly and easy method for constructing tubular structure of metal oxides with different diameters for various applications.

Hollow ZnO microspheres with tunable interior architecture are successfully synthesized by a simple green chemistry routes at low temperature. This process is environmentally friendly processing, which based on without using solvents, employing carbon microspheres as template and reaction at low temperature. The layer-control of hollow ZnO microspheres can be easily adjusted by varying the concentration of the zinc precursor added. To demonstrate the usage of such hollow ZnO microspheres, gas sensors have been fabricated from the as-synthesized hollow ZnO microspheres with different shelled and investigated for formaldehyde (HCHO) detection. Interestingly, the response of hollow ZnO microspheres increased with increasing the number of shell structures. These results indicate that three-shelled ZnO sensor displays about 1.5 and 3–4 fold enhancement in response compared to double and single-shelled one, respectively. The mechanism of enhanced sensor performances is also proposed.

Graphene-based films are widely used in the electronics industry. Here, surface hydroxylated graphene sheets (HGS) have been synthesized from natural graphite (NG) by a rapid and efficient molten hydroxide-assisted exfoliation technique. This method enables preparation of aqueous dispersible graphene sheets with a high dispersed concentration (~10.0 mg ml−1) and an extraordinary production yield (~100%). The HGS dispersion was processed into graphene flexible film (HGCF) through fast filtration, annealing treatment and mechanical compression. The HGS endows graphene flexible film with a high electrical conductivity of 11.5 × 104 S m−1 and a superior thermal conductivity of 1842 W m−1 K−1. Simultaneously, the superflexible HGCF could endure 3000 repeated cycles of bending or folding. As a result, this graphene flexible film is expected to be integrated into electronic packaging and high-power electronics applications.

New Au@SnO2 yolk-shell nanospheres have been successfully synthesized by using Au@SiO2 nanospheres as sacrificial templates. This process is environmentally friendly and is based on hydrothermal shell-by-shell deposition of polycrystalline SnO2 on spheriform Au@SiO2 nanotemplates. Au nanoparticles can be impregnated into the SnO2 nanospheres and the nanospheres show outer diameters of 110 nm and thicknesses of 15 nm. The possible growth model of the nanospheres is proposed. The gas sensing properties of the Au@SnO2 yolk-shell nanospheres were researched and compared with that of the hollow SnO2 nanospheres. The former shows lower operating temperature (210 °C), lower detection limit (5 ppm), faster response (0.3 s) and better selectivity. These improved sensing properties were attributed to the catalytic effect of Au, and enhanced electron depletion at the surface of the Au@SnO2 yolk-shell nanospheres.

New Au@SnO2 yolk–shell nanospheres have been successfully synthesized by using Au@SiO2 nanospheres as sacrificial templates. This process is environmentally friendly and is based on hydrothermal shell-by-shell deposition of polycrystalline SnO2 on spheriform Au@SiO2 nanotemplates. Au nanoparticles can be impregnated into the SnO2 nanospheres and the nanospheres show outer diameters of 110 nm and thicknesses of 15 nm. The possible growth model of the nanospheres is proposed. The gas sensing properties of the Au@SnO2 yolk–shell nanospheres were researched and compared with that of the hollow SnO2 nanospheres. The former shows lower operating temperature (210 °C), lower detection limit (5 ppm), faster response (0.3 s) and better selectivity. These improved sensing properties were attributed to the catalytic effect of Au, and enhanced electron depletion at the surface of the Au@SnO2 yolk–shell nanospheres.