Porous Organic Polymer Supported Pd/Cu Bimetallic Catalyst for Heterogeneous Oxidation of Alkynes to 1,2-Diketones

A porous organic polymer (POP-POPh3) was readily prepared by oxidation of POP-PPh3 with H2O2. After coordination with PdCl2 and co-catalyst of CuBr2 precursor, a Pd/Cu bimetals-loaded porous organic polymer (Pd/Cu@POP-POPh3)...

In-Situ FTIR Study of Heterogeneous Oxidation of SOA Tracers by Ozone

Secondary organic aerosols (SOA) play an important role in global climate change and air quality, and SOA tracers can directly characterize the source and reaction mechanism of SOA. However, it is not well known that whether the tracers can be oxidized or how the instability of the tracers in the atmosphere. In this paper, in-situ FTIR was used to analyze the chemical structure changes of erythritol, analogue of 2-methyl erythritol (AME) that is, a tracer of isoprene SOA, and 2, 3-dihydroxy-4-oxopentanoic acid (DHOPA), a tracer of toluene SOA, when exposed to high concentration of ozone for short periods. Under the condition of 20 ppm ozone exposure for 30 min, the change rate of absorption area of AME at 3,480 and 1700 cm−1 was −0.0134 and 0.00117 int.abs/s, respectively, and the change rate of the absorption area of DHOPA at 1,640 and 3340cm−1 was −0.00191 and 0.00218 int.abs/s, respectively. The pseudo-first-order reaction rate constant kapp were 1.89 × 10−8 and 2.12 × 10−7 s−1, and the uptake coefficients of ozone on the surface of AME and DHOPA were (1.3 ± 0.8) × 10−8 and (4.5 ± 2.7) × 10−8, respectively. These results showed the oxidation processes of AME and DHOPA were slow in the presence of high concentrations of ozone, which implied that AME and DHOPA could be considered to be stable in the atmospheric environment with ozone as the main oxidant.

Selective C–C Bond Cleavage in Diols and Lignin Models: High-Throughput Screening of Metal Oxide-Anchored Vanadium in Mesoporous Silica

The development of selective and robust heterogeneous oxidation catalysts is an enabling technology for conversion of biomass-derived platform chemicals. Vanadium active sites were incorporated into the structure of mesoporous silica via an ultra-fast, one-pot synthesis method based on microwave-assisted heating. In addition, Al/Ti/Zr/Ce anchoring ions were introduced in order to minimize vanadium leaching and better control its dispersion. The supported V-(Al/Ti/Zr/Ce)-MCM-41 composite materials were assessed as catalysts for aerobic C–C bond cleavage of simple models for lignin (1,2-diphenyl-2-methoxyethanol) and sugar-derived polyalcohols (meso-hydrobenzoin). The TiIV ions proved to be the best anchors to prevent V leaching, while AlIII and ZrIV ions were the best to improve selective conversion of the substrates. The active sites in these catalysts are shown to be 2D VOx layers stabilized on the anchors. In a screen of twelve solvents, weakly polar solvents like toluene were found to be most suitable for this reaction, as was environmentally friendly ethyl acetate. The above properties, together with the high selectivity for C–C bond cleavage, advocate for a heterogeneous catalytic pathway, intrinsically different from that reported previously for molecular oxovanadium (V) catalysts.

Oxidation of Cr(III) to Cr(VI) and Production of Mn(II) by Synthetic Manganese(IV) Oxide

The heterogeneous oxidation of Cr(III) to Cr(VI), a toxic inorganic anion, by a synthetic birnessite (δ-MnO2) was investigated in batch reactions using a combination of analytical techniques including UV–Vis spectrophotometry, microwave plasma–atomic emission spectrometry, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectroscopy (FTIR), to evaluate both the solution speciation of Cr(III)/Cr(VI) and the surface of the reacted δ-MnO2. The formation of dissolved Mn(II) was determined during the batch reactions to evaluate the extent and stoichiometry of the Cr(III) oxidation reaction. A stoichiometric 3:2 Mn(II):Cr(VI) molar relationship was observed in the reaction products. The reductive dissolution of the δ-MnO2 by Cr(III) resulted in a surface alteration from the conversion of Mn(IV) oxide to reduced Mn(II) and Mn(III) hydroxides. The results of this investigation show that naturally occurring Cr(III) will readily oxidize to Cr(VI) when it comes in contact with MnO2, forming a highly mobile and toxic groundwater contaminant.