The g-C(3)N(4) photocatalyst was synthesized by directly heating the low-cost melamine. The methyl orange dye (MO) was selected as a photodegrading goal to evaluate the photocatalytic activity of as-prepared g-C(3)N(4). The comparison experiments indicate that the photocatalytic activity of g-C(3)N(4) can be largely improved by the Ag loading. The strong acid radical ion (SO(4)(2-) or NO(3)(-)) can promote the degrading rate of MO for g-C(3)N(4) photocatalysis system. The MO degradation over the g-C(3)N(4) is mainly attributed to the photoreduction process induced by the photogenerated electrons. Our results clearly indicate that the metal-free g-C(3)N(4) has good performance in photodegradation of organic pollutant.

Graphitic carbon nitride (g-C(3)N(4)) and boron-doped g-C(3)N(4) were prepared by heating melamine and the mixture of melamine and boron oxide, respectively. X-ray diffraction, X-ray photoelectron spectroscopy, and UV-vis spectra were used to describe the properties of as-prepared samples. The electron paramagnetic resonance was used to detect the active species for the photodegradation reaction over g-C(3)N(4). The photodegradation mechanisms for two typical dyes, rhodamine B (Rh B) and methyl orange (MO), are proposed based on our comparison experiments. In the g-C(3)N(4) photocatalysis system, the photodegradation of Rh B and MO is attributed to the direct hole oxidation and overall reaction, respectively; however, for the MO photodegradation the reduction process initiated by photogenerated electrons is a major photocatalytic process compared with the oxidation process induced by photogenerated holes. Boron doping for g-C(3)N(4) can promote photodegradation of Rh B because the boron doping improves the dye adsorption and light absorption of catalyst.

Multimetal mesoporous materials MGa2O4 (M=Zn, Ni, Co) can be synthesized by ion‐exchange reactions of colloidal mesoporous NaGaO2 (see scheme with TEM images), which acts as both template and precursor, so that a template‐removal process can be dispensed with.

Basically super: Potassium‐functionalized mesoporous γ‐alumina solid superbases that have a high base strength (H−) of 27.0, a well‐expressed mesoporous structure, and which are efficient in the isomerization of 1‐hexene are synthesized by a one‐pot method. The success of this method can be ascribed to the flexible application of K2CO3 as a pH adjustor and close control of the calcination process (see picture).