Effect of the Reaction Temperature on the Removal of Diesel Particulate Matter by Ozone Injection

This study seeks to investigate the removal efficiency of particulate matter (PM) from the actual diesel exhaust at various reaction temperatures by using non-thermal plasma (NTP). The effect of the reaction temperature on removal efficiency was reflected by the change in the concentration of particles in different modes and the weight fraction of volatile organics in PM. The Arrhenius equation was used to determine the apparent activation energies E_a of the soot in PM. In addition, the difference in the oxidation reaction at various reaction temperatures and the effect of NTP on the properties of PM were discussed. After considering the decreasing ranges of the total concentration and the weight of the PM, it was determined that 120 °C is the optimal temperature choice for PM removal. The decreasing range of the total concentration reached 57.13% and 66.79% of PM was removed when the PM is measured by weight. NTP has better effect on the removal of smaller particles. The weight fraction of the volatile fraction markedly decreases after the reaction and the apparent activation energy of soot noticeably decreased. The oxidizability of the excited species in NTP was enhanced with the increase of the reaction temperature. However, the excited species concentration declined concurrently, resulting in the occurrence of the optimized range of reaction temperature. The particles were removed by the oxidation that occurred on the surface of the primary particle and the disintegration of the structure of the particles.

     

Room temperature suzuki cross‐coupling polymerizations of aryl dihalides and aryldiboronic acid/acid esters with t‐Bu3P‐coordinated 2‐phenylaniline‐based palladacycle complex as the precatalyst

Room temperature Suzuki cross‐coupling polymerization of aryl dibromides/diiodides with aryldiboronic acids/acid esters with t‐Bu₃P‐coordinated 2‐phenylaniline‐based palladacycle complex, [2′‐(amino‐kN)[1,1′‐biphenyl]‐2‐yl‐kC]chloro(tri‐t‐butylphosphine)palladium, as a general precatalyst is described. Such room temperature Suzuki cross‐coupling polymerization is achieved by employing six equivalents or more of the base and affords polymers within an hour, with the yields and the molecular weights in general comparable to or higher than reported results that required higher reaction temperature and/or longer polymerization time. Our study provides a general catalyst system for the room temperature Suzuki cross‐coupling polymerization of aryl dibromides/diiodides with aryldiboronic acids/acid esters and paves the road for the investigation of employing other monodentate ligand‐coordinated palladacycle complexes including other electron‐rich monophosphine‐coordinated ones for room temperature cross‐coupling polymerizations. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019, 57, 1606–1611     

Enantioselective Synthesis of a Chiral Coordination Polymer with Circularly Polarized Visible Laser

Circular dichroism is known to be the feature of a chiral agent which has inspired scientist to study the interesting phenomena of circularly polarized light (CPL) modulated molecular chirality. Although several organic molecules or assemblies have been found to be CPL‐responsive, the influence of CPL on the assembly of chiral coordination compounds remains unknown. Herein, a chiral coordination polymer, which is constructed from achiral agents, was used to study the CPL‐induced enantioselective synthesis. By irradiation with either left‐handed or right‐handed CPL during the reaction and crystallization, enantiomeric excesses of the crystalline product were obtained. Left‐handed CPL resulted in crystals with a left‐handed helical structure, and right‐handed CPL led to crystals with a right‐handed helical structure. It is exciting that the absolute asymmetric synthesis of a chiral coordination polymer could be enantioselective when using CPL, and provides a strategy for the control of the chirality of chiral coordination polymers.