Detailed potentiodynamic and galvanostatic methods have been used to investigate the electrodeposition of Zn and to develop a reliable recovery method from a purified and concentrated spent pickling liquor (SPL) of hot dip galvanization. Applying various combinations of Zn concentration, pH, agitation, apparent current density (c.d.) and additional NaCl concentration, a uniform initial deposit could be observed at the cathode, however the subsequent dendrite formation and the development of protrusion at the edges were targeted for a deeper investigation. The potentiodynamic experiments, showed the importance of H2 evolution influenced by the electrolyte properties and the cathodic polarization. The cathodic current was dominated by Zn reduction in the pH > 2 range during the fast potentiodynamic runs of the 30 – 150 g/dm3 Zn concentration range in the stationary electrolyte. Increasing the Zn concentration could considerably improve the deposit morphology. In the long-term galvanostatic experiments the current efficiency increased with the increase of pH in the examined wide Zn concentration range but the c.d. needs optimization. A current efficiency (c.e.) of ~99% can be reached with an electrolyte of pH ~5, Zn concentration ~50 g/dm3 applying a c.d. in the 300 – 600 A/m2 range. At low (~10 g/dm3) Zn concentrations the rate of hydrogen evolution increases dramatically. The addition of NaCl can practically improve the c.e. if the Zn concentration is at least around 50 g/dm3. In contrast, this improvement is largely off-set by the negative effects of strong H2 evolution at as low Zn concentrations as e.g. 10 g/dm3. Higher NaCl additions or too high Cl- ion concentrations, however inhibit the cathodic reaction of the electroactive species by stronger chloro-complex formation. In this case the intensive H+ reduction causes hydroxide precipitation.