Anthropogenically derived phosphate-bearing crystalline materials serve as reactive surfaces for nutrient recycling to the environment. The reactivity of these surfaces is critical for controlling nutrient release rates and will depend on the relative humidity at the soil surface. In this study, we investigate water uptake on these phosphate-bearing minerals as a function of relative humidity. In particular, this study is focused on the water adsorption properties of two anthropogenically derived phosphates, hydroxyapatite (HAP) and struvite. HAP exhibited a stable surface structure, and the water adsorption data were fit using Brunauer− Emmett−Teller (BET) and Freundlich adsorption models. Struvite surface, on the other hand, exhibited intrinsic instability due to the crystalline water loss at very low relative humidity, leading to the adsorption data not being well described by traditional models. Diffuse reflectance infrared spectroscopy studies showed that a relative humidity of <5% resulted in crystalline water removal, as well as the change in the structure of the hydrogen-bonded surface water and the ammonium ions in the struvite crystals. HAP exhibited a calculated heat of sorption that converged to the water heat of liquefication, while struvite exhibited transient behavior, which resulted in a nonconvergent calculated heat of sorption.