N-Heterocyclic Carbenes in Late Transition Metal Catalysis

It is well known that urbanization and industrialization have resulted in the rapidly increasing emissions of volatile organic compounds (VOCs), which are a major contributor to the formation of secondary pollutants (e.g., tropospheric ozone, PAN (peroxyacetyl nitrate), and secondary organic aerosols) and photochemical smog. The emission of these pollutants has led to a large decline in air quality in numerous regions around the world, which has ultimately led to concerns regarding their impact on human health and general well-being. Catalytic oxidation is regarded as one of the most promising strategies for VOC removal from industrial waste streams. This Review systematically documents the progresses and developments made in the understanding and design of heterogeneous catalysts for VOC oxidation over the past two decades. It addresses in detail how catalytic performance is often drastically affected by the pollutant sources and reaction conditions. It also highlights the primary routes for catalyst deactivation and discusses protocols for their subsequent reactivation. Kinetic models and proposed oxidation mechanisms for representative VOCs are also provided. Typical catalytic reactors and oxidizers for industrial VOC destruction are further discussed. We believe that this Review will provide a great foundation and reference point for future design and development in this field.

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Recent Advances in the Catalytic Oxidation of Volatile Organic Compounds: A Review Based on Pollutant Sorts and Sources.

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Surface chemistry of catalysis by gold

Hypercrosslinked polymers (HCPs) are a series of permanent microporous polymer materials initially reported by Davankov, and have received an increasing level of research interest. In recent years, HCPs have experienced rapid growth due to their remarkable advantages such as diverse synthetic methods, easy functionalization, high surface area, low cost reagents and mild operating conditions. Judicious selection of monomers, appropriate length crosslinkers and optimized reaction conditions yielded a well-developed polymer framework with an adjusted porous topology. Post fabrication of the as developed network facilitates the incorporation of various chemical functionalities that may lead to interesting properties and enhance the selection toward a specific application. To date, numerous HCPs have been prepared by post-crosslinking polystyrene-based precursors, one-step self-polycondensation or external crosslinking strategies. The advent of these methodologies has prompted researchers to construct well-defined porous polymer networks with customized micromorphology and functionalities. In this review, we describe not only the basic synthetic principles and strategies of HCPs, but also the advancements in the structural and morphological study as well as the frontiers of potential applications in energy and environmental fields such as gas storage, carbon capture, removal of pollutants, molecular separation, catalysis, drug delivery, sensing etc.

Hypercrosslinked porous polymer materials: design, synthesis, and applications

Graphene has a unique atom-thick two-dimensional (2D) structure, high conductivity and charge mobility, huge specific surface area, excellent mechanical, thermal and electrical properties. Thus, it has been regarded as an important component for functional materials, especially for developing a variety of catalysts. In this review, we summarize the recent advancements in synthesizing graphene based new catalysts, and their applications in organic synthesis, sensors, environmental protection and energy related systems.

Graphene based catalysts

Complete oxidation of formaldehyde at ambient temperature over supported Pt/Fe2O3 catalysts prepared by colloid-deposition method

Catalytic oxidation of formaldehyde over different silica supported platinum catalysts

Adsorption behaviors of methyl orange dye on nitrogen-doped mesoporous carbon materials.

A kind of highly efficient and low cost supported-Pt catalyst for oxidation of toluene is obtained through controlling both the chemical state of Pt active sites and surface properties of supports. The optimized Pt/Al2O3 catalyst with Pt loading as low as 0.1 wt% could completely convert toluene (1000 ppm) to CO2 at about 180 ℃ under a space velocity of 24,000 mL g−1 h−1. It also exhibits a high stability and moisture resistance properties under reaction atmosphere. TOF value calculated with the dispersion of Pt can reach 0.0685 s-1, representing a high utilization efficiency of Pt. A series of characterizations are carried out to investigate the key factors affecting the catalytic performance of Pt/Al2O3, and disclose the concrete role of Pt and Al2O3 in the activation of molecular oxygen and toluene. In situ DRIFTS and EPR results show that Pt is the active center for O2 activation. Metallic Pt nanoparticles (Pt0) can activate the molecular O2 even at room temperature. Al2O3 offers sites for the adsorption of toluene and desorption of CO2 product. The weak and medium strength of acid-base sites favorite the adsorption and desorption process. The oxidation of toluene over Pt/Al2O3 obeys modified L-H mechanism. The synergistic effect of metallic Pt nanoparticles and suitable Al2O3 support is critical for obtaining highly efficient Pt-based catalysts with low Pt contents for toluene oxidation.

Wenxiang Zhang

Papers

Complete oxidation of formaldehyde at ambient temperature over supported Pt/Fe2O3 catalysts prepared by colloid-deposition method

Catalytic oxidation of formaldehyde over different silica supported platinum catalysts

Adsorption behaviors of methyl orange dye on nitrogen-doped mesoporous carbon materials.

Pt/Al2O3 with ultralow Pt-loading catalyze toluene oxidation: Promotional synergistic effect of Pt nanoparticles and Al2O3 support

Low-temperature CO oxidation over supported Pt catalysts prepared by colloid-deposition method