Isomorphous Substitution in ZSM-5 in Tandem Methanol/Zeolite Catalysts for the Hydrogenation of CO 2 to Aromatics
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A precision polymer featuring one phenyl pendant at every fifth carbon on a polyethylene backbone was modified to varying degrees of sulfonation (DS = 33–98%) using acetyl sulfate with standard conditions by varying reaction times (up to 48 h). This soft, homogeneous method allows for evenly distributed phenylsulfonic acid groups with minimal side reactions and results in light brown, transparent materials with glass transition temperatures of 33–78 °C that increase with DS and parent polymer molar mass. The DS was accurately determined through well-resolved 1 H NMR (DSHNMR) signals of the regularly spaced phenyl groups and corroborated by inverse-gated decoupling 13 C NMR analysis. These analyses were compared to a series of other commonly accepted methods for DS determination including titration and elemental analysis (EA). The DS by titration (DS titr ) also increased with reaction time but was consistently lower than those determined by NMR. Significant discrepancies between theoretical and measured sulfur mass were observed for several samples through EA. Qualitative methods, such as infrared spectroscopy and thermal analyses, were also performed and correlated well with the DS determined by NMR. Here, this study presents a promising method to achieve a complete scope of homogeneous sulfonation from mild reaction conditions and presents a case to determine DS through multiple methods, with spectroscopic analyses, such as NMR, being potentially the most valuable.
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The objective of this project is to pursue enhanced yields of benzene, toluene, and xylene (BTX) from catalytic fast pyrolysis (CFP) of biomass by recycling a portion of the bio-oil back to the pyrolyzer. Additionally, this work evaluated the impact of CFP process variables on the yields of BTX.
RNA-seq comparison of transcript abundance in a PDC-producing N. aromaticivorans strain (12444PDC) grown in the presence of dehydrodiconiferyl alcohol (DC-A) and glucose, vanillin and glucose, ferulic acid and glucose, or glucose alone
Formation of intermediate during periodate oxidation of catechol that subsequently decomposes
Aromatic/heterocyclic polymers from tetraamines reaction with tetraacids at room temperature, developing potential for aerospace application
Torsional creep and creep recovery behavior of amorphous 1, 3, 5-tri-alpha-naphthyl benzene close to or below glass transition temperature
Crystal growth, nucleation, supercooling, solidification, glass forming and kinetics of 1, 3, 5-tri-alpha-naphthylbenzene
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