Carbon capture has been a highly sought-after technology for decades because of its<br/>capabilities to restore atmospheric damage done by greenhouse gasses. Thanks to evolving<br/>separation techniques, carbon capture is becoming more efficient with every new discovery in<br/>the field. Currently the biggest problems that carbon capture are facing is the cost of<br/>manufacturing material to aid the process and obtaining ideal conditions for removal of carbon<br/>from air and devising solutions for removal of CO2 in ambient and flue gas conditions.<br/>This Honors Thesis is a continuation of Dr. Shuguang Deng and Dr. Mai Xu’s research<br/>initiative to manufacture and test various zeolitic CO2 removal efficiencies. The goals of this<br/>Honors Thesis are to investigate the adsorption/desorption kinetics and isothermal equilibrium<br/>CO2 capacity of a NaX nanozeolite under ambient air conditions.<br/>What was determined from the following testing was that the zeolite of interest had a<br/>higher adsorption capacity of CO2 at lower temperatures, had a maximum equilibrium quantity<br/>adsorbed of 0.203 mmol/g for CO2 and 0.367 mmol/g of N2, had a maximum breakthrough CO2<br/>capacity of 0.101 mmol of CO2 per gram of zeolite at dry conditions and 298.15K and this<br/>linearly decreased to 0.040 mmol/g at 25% relative humidity.

Plastic consumption has reached astronomical amounts. The issue is the single-use plastics that continue to harm the environment, degrading into microplastics that find their way into our environment. Finding sustainable, reliable, and safe methods to break down plastics is a complex but valuable endeavor. This research aims to assess the viability of using biochar as a catalyst to break down polyethylene terephthalate (PET) plastics under hydrothermal liquefaction conditions. PET is most commonly found in single-use plastic water bottles. Using glycolysis as the reaction, biochar is added and assessed based on yield and time duration of the reaction. This research suggests that temperatures of 300℃ and relatively short experimental times were enough to see the complete conversion of PET through glycolysis. Further research is necessary to determine the effectiveness of biochar as a catalyst and the potential of process industrialization to begin reducing plastic overflow.

Ammonia is one of the most critical chemical commodities produced and is integral to a number of current industries such as agriculture as well as a key part to future sustainability areas such as clean H2 production. However, the current production methods for ammonia are largely unsustainable and produce large amounts of CO2 emissions. This combined with the current dependence on fossil energy for production has led to researchers attempting to develop a clean and sustainable method for ammonia production. This method involves the thermochemical looping of a nitride compound with H2, and the renitridation of the compound with N2. This thermochemical loop would significantly reduce pressure requirements for ammonia production in addition to only being reliant on renewable inputs. This paper expands and complements this research by detailing the methods for the synthesis of nitride compounds as well as confirming their structure through material characterization. The nitride compounds as well as their oxide precursors were synthesized through Pechini synthesis and co-precipitation, and their structure was confirmed through the use of X-ray diffraction analysis. The XRD patterns of the synthesized nitrides matched those previously synthesized as well as those found in literature. In addition, observation of the spectra for the oxide CoMoO4 showed a marked similarity to that of the oxide precursor for (NixCox)2Mo3N. However, further testing is necessary regarding the phase-purity of synthesized nitrides, as well as the reduction and renitridation capability of nitrides in the line of (NixCox)2Mo3N.