Effect of mechanical-chemical modification on adsorption of beryllium by calcite.

The treatment of beryllium wastewater has become a major problem in industry. In this paper, CaCO3 is creatively proposed to treat beryllium-containing wastewater. Calcite was modified by an omnidirectional planetary ball mill by a mechanical-chemical method. The results show that the maximum adsorption capacity of CaCO3 for beryllium is up to 45 mg/g. The optimum treatment conditions were pH = 7 and the amount of adsorbent was 1 g/L, and the best removal rate was 99%. The concentration of beryllium in the CaCO3-treated solution is less than 5 µg/L, which meets the international emission standard. The results show that the surface co-precipitation reaction between CaCO3 and Be (II) mainly occurs. Two different precipitates are generated on the used-CaCO3 surface; one is the tightly connected Be (OH)2 precipitation, and the other is the loose Be2(OH)2CO3 precipitation. When the pH of the solution exceeds 5.5, Be2+ in the solution is first precipitated by Be (OH)2. After CaCO3 is added, CO32- will further react with Be3(OH)33+ to form Be2(OH)2CO3 precipitation. CaCO3 can be considered as an adsorbent with great potential to remove beryllium from industrial wastewater.

Adsorptive removal of beryllium by Fe-modified activated carbon prepared from lotus leaf.

Lotus leaf was used as raw material to prepare HNO3-activated carbon with 1.5:1 (HNO3:lotus leaf) (wt:wt) impregnation. Then, the activated carbon was modified by Fe(NO3)3 to obtain Fe-activated carbon (Fe-AC). The adsorption test results show that Fe-AC maximum saturated adsorption capacity (Qm) is 45.68 mg/g when the Fe(NO3)3 loading is 5% of the total activated carbon, pH = 6, and the temperature is 35 ℃. The adsorption effect of Fe-AC under neutral conditions is better than that under alkaline and acidic conditions. The modified activated carbon has better adsorption selectivity. The obtained material (Fe-AC) was characterized by N2 adsorption-desorption isotherm, SEM, FT-IR, BET, XRD, XPS, and pHpzc. The total pore volume, specific surface area, and zero charges of modified activated carbon were increased. The types of modified functional groups were reduced, and the iron reacted with the functional groups, providing ion exchange sites for the adsorption of beryllium. The adsorption thermodynamics showed that the adsorption process was spontaneous and endothermic. The adsorption mechanism of Fe-AC to beryllium is mainly chemical adsorption.