Metal oxide-supported Au catalysts, particularly those with small Au nanoparticles, catalyze a variety of reactions including low-temperature CO oxidation and selective hydrogenation of alkynes. However, the facile nature of Au particle growth at even moderate temperatures poses significant challenges to maintaining catalyst activity under reaction conditions. Here, we present a method to reduce the rate of sintering and coke formation in TiO2-supported Au catalysts via the deposition of alkyl-phosphonic acid (PA) self-assembled monolayers. After surface modification with PAs, the resultant catalysts exhibited significantly improved resistance to Au sintering. PA deposition strongly suppressed CO oxidation rates, consistent with poisoning of active sites. In contrast, modification with PAs significantly improved the rate of C2H2 hydrogenation on Au/TiO2. The enhanced activity was accompanied by a dramatically improved resistance to accumulation of surface carbonaceous species.

1,2,3-Trimethoxypropane (1,2,3-TMP) is the trimethyl ether of propane-1,2,3-triol, better known as glycerol, which can be derived from triglycerides originating from either plant or animal sources. Despite its simple structure and the ubiquity of its glycerol precursor, successful synthesis of 1,2,3-TMP was only recently reported in the literature, with studies suggesting it may be a "green" and nontoxic alternative to solvents such as diglyme, a constitutional isomer. However, no thermophysical properties of 1,2,3-TMP have yet been reported. Furthermore, the structure of 1,2,3-TMP is also analogous to polyether solvents used in the Selexol process for removal of CO 2 and other "acid" gases from CH 4 , H 2 , etc. As such, examining the solubility of CO 2 in 1,2,3-TMP is also of interest. This work details our initial studies and characterization of 1,2,3-TMP as a physical solvent for CO 2 absorption, as well as the characterization of its density, viscosity, and vapor pressure with respect to temperature. 1,2,3-TMP exhibits favorable properties, and glycerol-derived triethers warrant deeper consideration as new solvents for CO 2 absorption and other gas treating applications.

The emergence of 3D printing has dramatically advanced the availability of tangible molecular and extended solid models. Interestingly, there are few nanostructure models available both commercially and through other do-it-yourself approaches such as 3D printing. This is unfortunate given the importance of nanotechnology in science today. In this work, we have filled part of this gap by designing and 3D printing several block copolymer (BCP) nanostructure morphologies. We used a variety of methods including manually drawing the files within 3D computer design software, using equations with mathematical graphing software, and developing a programming script to convert self-consistent field theory (SCFT) structure data into a 3D printable file. Conversion of SCF data into 3D printable structures may find broader applicability beyond creating BCP nanostructures as SCF calculations are used in a variety of geometric computations. All methods reported herein produced tangible 3D prints of approximately equal quality. These tangible models will be useful for educators, students, and researchers in polymer science and nanotechnology.

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