Vapor sensing with color-tunable multilayered coatings of cellulose nanocrystals.

Colloidal cellulose nanocrystals were LBL deposited to form firmly-stacked optical coatings in which the nanorods regulated their head-to-tail association and aligned in the axial-centrifuged direction. The periodically transition from blue to orange of reflected colors was tunable via deposition layer adjustment. While the sensing coating was exposed to vapors of NH3.H2O, H2O, HCl and HAc, respectively, the color variation in the response process was irreversible at room temperature and highly dependent on vapor diffusion and chemical interface interaction. Consequently, HAc vapor presented the longest sensing transition of wavelength, whereas the alkaline NH3.H2O displays a less recovery ratio than HAc and H2O at room temperature. Under heating at 50°C, the sensed coatings could mostly be restored to their original state except HCl-etched one. Therefore, the naked-eyed qualitative detectability of vapors by nanocellulose could be realized by the divergence in color shift which is of great importance in chemical sensors.

The naked-eye detection of NH(3) -HCl by polyaniline-infiltrated TiO(2) inverse opal photonic crystals.

A reversible color change of a polyaniline-infiltrated TiO(2) inverse opal photonic crystal (PC) film can be obtained when the PC is switched from an acidic to alkali vapor environment. In a saturated NH(3) environment, the stopband of the as-prepared PCs changes from 556 to 688 nm; such large shift of 132 nm could be observed, corresponding to a clear color change from green to red. After placing in HCl vapor, the stopband undergoes a blue-shift and the color turns back to green. The result is ascribed to PANI being doped or dedoped by acid or base and the effective refractive index of the PC film varying accordingly. The naked-eye detection of NH(3) and HCl vapors can be realized by the reversible color change of the PC film, which is of importance for chemical and biological sensors.

Facile synthesis of hollow Co3O4 microspheres and its use as a rapid responsive CL sensor of combustible gases.

The hollow Co(3)O(4) microspheres (HCMs) were prepared by the carbonaceous templates, which did not need the surface pretreatment. The chemiluminescence (CL) and catalytic properties for CO oxidation over these hollow samples were evaluated. The samples were characterized by scanning electron microscopy (SEM), energy disperse spectra (EDS), transmission electron microscopy (TEM), selected area electron diffraction (ED), X-ray diffraction (XRD), temperature-programmed desorption (TPD) and N(2) adsorption. The influences of filter' band length, flow rate of gas, test temperature, and particle structure on CL intensities were mainly investigated. It was found that compared with the solid Co(3)O(4) particles (SCPs), HCMs had a stronger CL intensity, which was ascribed to its hollow structure; and that CL properties of the catalysts were well correlated with their reaction activities. Moreover, HCMs were used to fabricate a highly sensitive gas detector, which is a rapid and effective method for the selection of catalysts or the detection of environmental deleterious gases.

Sonodegradation of halomethane mixtures in chlorinated drinking water.

Ultrasonic degradation of halomethane mixtures, with very low initial concentration in chlorinated drinking water was investigated. It was observed that the removal efficiencies of four halomethanes after 1 h ultrasonic irradiation followed the increasing order: CHCl(3) < CHBr(2)Cl < CHBrCl(2) < CCl(4) and the degradation reactions of the halomethanes were well described by the pseudo-first-order kinetics model. Molecular polarity was found to be an important factor controlling the sonodegradation of halomethane mixtures. Increasing acoustic intensity enhanced the removal of halomethanes in chlorinated drinking water. In addition, ultrasonic irradiation led to a slightly decrease of pH and TOC of chlorinated drinking water.