The column sits at the end of the ammonia oxidation train. Ammonia burns over platinum-rhodium gauze to NO, the stream is cooled, and NO reacts with residual oxygen to form NO2 and its dimer N2O4. Per EPA AP-42, Section 8.8, the cooled mixture enters the bottom of the column while deionized water is fed at the top, and the two flow countercurrent.
Two reactions alternate along the height. On sieve or bubble-cap trays, NO2 dissolves and reacts: 3NO2 + H2O → 2HNO3 + NO. In the free space between trays, the released NO is re-oxidized: 2NO + O2 → 2NO2. This second reaction is slow, homogeneous, and favored by low temperature and high pressure. That is why the inter-tray volume is generous and why cooling coils are built directly into the trays: both reactions are exothermic, and every degree removed pushes the equilibrium toward HNO3.
A NOx absorption tower in a modern dual-pressure plant runs at 8–14 bar even though ammonia oxidation upstream prefers low pressure; a dedicated compressor between the two stages pays for itself in recovered product. Acid leaves the bottom at 55–68% HNO3, and secondary air strips dissolved NO2 from it in a bleacher. Final strength depends on pressure, coolant temperature, tray count, and inlet NOx concentration; across the industry, weak product spans 30–70% HNO3, and stage count is the main lever.