Catalytic Conversion of Carbon Dioxide to Long Chain Esters via Formate Hydroesterification.

CO2-based hydroesterification is an attractive route to produce value added ester compounds, which could replace CO-based hydroesterification processes if sufficient catalytic technologies are developed. One path to CO2-based hydroesterification is through an organoformate intermediate, which is then used in olefin hydroesterification to generate the desirable esters.  This route creates a net CO2-based hydroesterification process using tandem catalytic systems for CO2 hydrogenation to organoformate paired with formate-olefin hydroesterification.

Amphiphilic Thiol Polymer Nanogel Removes Environmentally Relevant Mercury Species from Both Produced Water and Hydrocarbons.

Technologies for removal of mercury from produced water and hydrocarbon phases are desired by oil and gas production facilities, oil refineries, and petrochemical plants. Herein, we synthesize and demonstrate the efficacy of an amphiphilic, thiol-abundant (11.8 wt % S, as thiol) polymer nanogel that can remove environmentally relevant mercury species from both produced water and the liquid hydrocarbon.

Impact of mercury speciation on its removal from water by activated carbon and organoclay.

Mercury (Hg) speciation can affect its removal efficiency by adsorbents. This study assessed the removal of dissolved inorganic Hg(II) species (Hg(II)*), β-HgS nanoparticles (HgS NP), and Hg complexed with dissolved organic matter (Hg-DOM) by three sorbents: activated carbon (AC), sulfur-impregnated activated carbon (SAC), and organoclay (OC). The effect of ionic composition, solution ionic strength, and natural organic matter (NOM) concentration on the removal of each Hg species was also evaluated.

Elemental Analysis of Asphaltenes Using Simultaneous Laser-Induced Breakdown Spectroscopy (LIBS)-Laser Ablation Inductively Coupled Plasma Optical Emission Spectrometry (LA-ICP-OES).

Laser-induced breakdown spectroscopy (LIBS) and laser ablation inductively coupled plasma optical emission spectrometry (LA-ICP-OES) were used simultaneously for the elemental analysis of asphaltene samples using minimum sample pretreatment in combination with low laser energy to reduce the amount of removed particles and avoid carbon deposits in the ablation cell. Quantitative analyses of S, Ni, and V were accomplished with LA-ICP-OES using external calibration with the C line as internal standard. The aromatic/paraffinic nature of the asphaltenes was also obtained throughout the H/C ratio using LIBS and partial least square regression model.

Influence of the dielectric medium on the carbonyl infrared absorption peak of acetylferrocene.

The solvent effect on the position of the carbonyl vibrational stretching of acetylferrocene in aprotic media was studied in this work. The solvent-induced shifts in this organometallic compound were interpreted in terms of the alternative reaction field model(SCRF-MO) proposed by Kolling. In contrast to the established trends for carbonyl groups in organic systems, the results suggest that the continuum models for the reaction field are not adequate and that the influence of dipolarity-polarizability described by an inhomogeneous coupling function theta(epsilon )L(n(2)) that assumes optical dielectric saturation is responsible for the carbonyl band shift and, there is empirical evidence that the effect of field-induced intermolecular interaction on band shift, interpreted in terms of the van der Waals forces from the solvent, have a important contribution to this phenomena.