UiO-66 is a Zr-based MOF that is being highly investigated for a wide variety of small molecule gas separations since it possess unprecedented thermal, chemical, and mechanical stability. In this work, we have investigated the performance of various functionalized variations of UiO-66 (UiO-66-OH, UiO-66-(OH)₂, UiO-66-NO₂, UiO-66-NH₂, UiO-66-SO₃H, and UiO-66-(COOH)₂) towards ammonia removal from air. Functionalized UiO-66 analogs have been synthesized solvothermally and characterized using ammonia breakthrough measurements under dry and humid (80% RH) air conditions along with powder X-ray diffraction (PXRD) patterns and results from BET modeling of N₂ adsorption isotherms. Counter to chemical intuition, our study demonstrates that the ammonia capacities of UiO-66-SO₃H and UiO-66-(COOH)₂ are lower than UiO-66-OH and UiO-66-NH₂. This is due to significant reduction in the framework porosity (surface area and pore volume) upon functionalization with bulky functional groups such as –COOH and –SO₃H. The –OH group is the least bulky functional group considered in the work and interacts favorably with ammonia. UiO-66-OH has a capacity of ~5.7 mmol/g for ammonia under dry conditions which is very close to the ammonia removal goal of 0.1 g/g MOF (or ~6 mmol/g). However, we observed a decrease in the ammonia capacities of functionalized UiO-66 variations under humid conditions due to competition between water and ammonia molecules for adsorption on the active sites. Overall, balancing the water adsorption behavior and high selectivity and high capacity for ammonia is crucial to developing new adsorbents for ammonia removal from air.