Lanthanum-doped ordered mesoporous hollow silica spheres were fabricated and utilized as phosphate adsorbents for the first time. Our prepared adsorbents exhibited spherical shapes with macropores in the center and ordered 2D hexagonal mesopores in the shell. By increasing the actual loading of La from 4.19 wt% to 22.44 wt%, the BET surface areas of the adsorbents decreased from 987.48 m 2 g À1 to 420.38 m 2 g À1 , coupled with a decline in average pore diameters and total pore volumes. In the batch adsorption tests, the adsorbents with greater amounts of La loading possessed markedly enhanced adsorption capacities; in contrast, the un-doped pure ordered mesoporous hollow silica particles could hardly adsorb any phosphate in solution. The adsorption isotherms of the La-doped ordered mesoporous hollow silica spheres were represented better by using the Langmuir model than the Freundlich model. The sample with 22.44 wt% La loading exhibited a maximum phosphate capture capacity of 47.89 mg P g À1 . In the kinetic study, its phosphate adsorption followed the pseudo-secondorder model well. Moreover, a dramatically fast kinetic adsorption was observed in the solution with a low phosphorus concentration of 2 mg P L À1 ; the adsorption equilibrium was reached in 15 min, with a 99.71% phosphate removal rate. High adsorption capacities were achieved within the pH range 3.0 to 8.0; relatively high selectivity to phosphate was observed in the presence of coexisting anions.
The present three-year field investigation
on sediment in the eutrophic
Pearl River in South China showed that concentrations of sulfonamides
(SAs), fluoroquinolones (FQs), and macrolides (MLs) in the river areas
where blooms occurred were 4.6, 2.4, and 3.4 times higher than those
without blooms, respectively, but the respective concentrations of
tetracycline (TC) and oxytetracycline (OTC) in the areas with blooms
were 2.6 and 3.8 times lower than those without. Significant positive
correlations were found between concentrations of chlorophyll a in water and most antibiotics in sediment. Further investigation
in each season suggested that lower diffusion but higher sinking were
possible reasons driving the burial of sulfapyridine (SPD), sulfamethoxazole
(SMX), and trimethoprim (TMP) in sediment from areas where blooms
occurred, with burial rates up to 14.86, 48.58, and 52.19 g month–1, respectively. Concentrations of TCs in both water
and sediment were inversely correlated with phytoplankton biomass,
which might be related to the enhanced biodegradation capacity of
bacteria caused by phytoplankton blooms. Phytoplankton also affected
concentrations of antibiotics in the snail, Bellamya purificata, with higher values in March but lower values in September. The
concentration of antibiotics in snails positively correlated with
that in sediment when snails were dormant but with antibiotics in
water after dormancy.
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