As a representative sulfur-containing volatile organic compounds (S-VOCs), CH₃SH has attracted widespread attention due to its adverse environmental and health risks. The performance of Mn-based catalysts and the effect of their crystal structure on the CH₃SH catalytic reaction have yet to be systematically investigated. In this paper, two different crystalline phases of tunneled MnO₂ (α-MnO₂ and β-MnO₂) with the similar nanorod morphology were used to remove CH₃SH, and their physicochemical properties were comprehensively studied using high-resolution transmission electron microscope (HRTEM) and electron paramagnetic resonance (EPR), H₂-TPR, O₂-TPD, Raman, and X-ray photoelectron spectroscopy (XPS) analysis. For the first time, we report that the specific reaction rate for α-MnO₂ (0.029 mol g⁻¹ h⁻¹) was approximately 4.1 times higher than that of β-MnO₂ (0.007 mol g⁻¹ h⁻¹). The as-synthesized α-MnO₂ exhibited higher CH₃SH catalytic activity towards CH₃SH than that of β-MnO₂, which can be ascribed to the additional oxygen vacancies, stronger surface oxygen migration ability, and better redox properties from α-MnO₂. The oxygen vacancies on the catalyst surface provided the main active sites for the chemisorption of CH₃SH, and the subsequent electron transfer led to the decomposition of CH₃SH. The lattice oxygen on catalysts could be released during the reaction and thus participated in the further oxidation of sulfur-containing species. CH₃SSCH₃, S⁰, SO₃²⁻, and SO₄²⁻ were identified as the main products of CH₃SH conversion. This work offers a new understanding of the interface interaction mechanism between Mn-based catalysts and S-VOCs.

With the development of miniaturization and integration of electrical and electronic equipment, the heat accumulation problems caused by the long-term operation of devices have become more and more serious. High thermal-conductivity and high-performance plastic composites have attracted significant interest from both academia and industry. Numerous studies have been recently conducted to enhance the thermal conductivity (TC) of nanofiller-filled polymeric composites. However, the homogeneous dispersion and directional arrangement of nanofillers in the resin matrix are the key factors limiting their effectiveness in enhancing thermal conductivity. Based on the feasibility considerations of mass production and industrial application, this paper reports on a novel preparation method of Poly(decamethylene terephthalamide)/graphite nanoparticle (GNP) nanocomposites with high thermal conductivity. Without borrowing solvents or other reagents, this method can effectively strip the inexpensive scaled graphite into nanoscale for its uniform dispersion and orientation arrangement by relying only on mechanical external forces. The whole technology is simple, green, and easy to industrialize. The fillers were well-dispersed and aligned in the PA10T, which played a role in significantly enhancing the thermal conductivity of the PA10T. In addition, we found that the thermal conductivity of the composites reached 1.20 W/(m·K) at 10 wt% filler content, which was 330% higher than that of the pure matrix. The mechanical properties of the composites were also significantly improved. This work provides guidance for the easy fabrication of thermally conductive composites with aligned structures.