We report on the synthesis of high-quality microporous/mesoporous BN material via a facile two-step approach. An extremely high surface area of 1687 m(2) g(-1) and a large pore volume of 0.99 cm(3) g(-1) have been observed in the synthesized BN porous whiskers. The formation of the porous structure was attributed to the group elimination of organic species in a BN precursor, melamine diborate molecular crystal. This elimination method maintained the ordered pore structure and numerous structural defects. The features including high surface area, pore volume and structural defects make the BN whiskers highly suitable for hydrogen storage and wastewater treatment applications. We demonstrate excellent hydrogen uptake capacity of the BN whiskers with high weight adsorption up to 5.6% at room temperature and at the relatively low pressure of 3 MPa. Furthermore, the BN whiskers also exhibit excellent adsorption capacity of methyl orange and copper ions, with the maximum removal capacity of 298.3 and 373 mg g(-1) at 298 K, respectively.
The semicrystalline polymer incorporated with nanofillers frequently exhibits complicated crystallization behavior, which is probably attributed to the nanofiller-constructed complex crystalline circumstance, especially a confined space. In the present work, in order to have a thorough understanding of biodegradable poly(L-lactic acid) (PLLA) crystallization behavior on the dependence of graphene oxide nanosheet (GONS) loadings, in particular the relatively high GONS loading, a set of GONS/PLLA nanocomposites with different GONS loadings ranging from 0 to 4.0 wt % were investigated in terms of isothermal crystallization behavior by differential scanning calorimetry and time-resolved Fourier-transform infrared spectroscopy techniques. The results indicated that GONSs not only served as heterogeneous nucleating agents for PLLA crystallization but also restricted the mobility and diffusion of PLLA chains. At low GONS concentrations of 0.25 and 0.5 wt %, GONSs acted as a temple for PLLA chains to land on due to extremely high specific surface area, thus promoting the conformational ordering and reducing the nucleating barrier. The nucleation effect of GONSs was dominant to achieve accelerated overall crystallization kinetics. As the GONS concentration rose up to 1.0 wt %, the GONS network was formed in the PLLA matrix, which was verified by solid-like rheological behavior at low frequencies in rheological measurement. The nanofiller network significantly constrained the mobility and diffusion of PLLA chains and offset the nucleation effect of GONSs, giving rise to a turning point in crystallization rate from promotion to restriction. Furthermore, a severely confined space was constructed by the more crowded and denser GONS networks at a higher GONS concentration of 4.0 wt %, compelling PLLA lamellae to grow in a two-dimensional mode. The unusual crystallization behavior of PLLA from promotion to restriction was also understood by the four-region model, in which the semiquantitative description of crystalline circumstance was provided. These results pave an effective way to further reveal the crystallization behavior of polymer at a relatively high nanofiller loading.
In conventional biomedical photoacoustic imaging systems, a pulsed laser is used to generate time-of-flight acoustic information of the subsurface features. This paper reports the theoretical and experimental development of a new frequency-domain (FD) photo-thermo-acoustic (PTA) principle featuring frequency sweep (chirp) and heterodyne modulation and lock-in detection of a continuous-wave laser source at 1064 nm wavelength. PTA imaging is a promising new technique which is being developed to detect tumor masses in turbid biological tissue. Owing to the linear relationship between the depth of acoustic signal generation and the delay time of signal arrival to the transducer, information specific to a particular depth can be associated with a particular frequency in the chirp signal. Scanning laser modulation with a linear frequency sweep method preserves the depth-to-delay time linearity and recovers FD-PTA signals from a range of depths. Preliminary results performed on rubber samples and solid tissue phantoms indicate that the FD-PTA technique has the potential to be a reliable tool for biomedical depth-profilometric imaging.
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