The enzymatic reduction of Hg(II) to water insoluble Hg(0)
by mercury resistant bacteria has been used for removal
of mercury from wastewater in technical scale. Pure cultures
of seven mercury resistant strains of Pseudomonas
were immobilized on carrier material inside a 700 L packed
bed bioreactor. Neutralized chloralkali electrolysis
wastewater with a mercury concentration of 3−10 mg/L
was continuously fed into the bioreactor (0.7 m3/h up to 1.2
m3/h). A mercury retention efficiency of 97% was obtained
within 10 h of inoculation of the bioreactor. At optimum
performance, bioreactor outflow concentrations were below
50 μg Hg/L, which fulfill the discharge limit for industrial
wastewater. In combination with an activated carbon filter,
outflow concentrations below 10 μg Hg/L were always
obtained. The retention efficiency of the bioreactor was
not affected by fluctuations in inflow conductivity (between
20 and 105 mS/cm), pH (between 6.5 and 7.5), or mercury
concentration (between 3 and 10 mg/L) and was between
95% and 99%. Temperature increases up to 47 °C did not
impair bioreactor performance. Standby periods up to 6
h could be tolerated without loss in activity. A simple, effective,
and robust biotechnology for remediation of mercury
polluted wastewater is thus demonstrated.