Preparation of sludge-cyanobacteria composite carbon for synergistically enhanced co-removal of Cu(II) and Cr(VI).

Traditional sludge disposal is currently restricted by the risk of secondary pollution. Sludge carbon material has gained widespread attention because of its low cost and environmentally sustainable properties. However, owing to the high ash content and low-energy density of sludge, sludge pyrolysis alone has certain limitations, and the performance of carbon materials needs to be improved. Herein, a sludge-cyanobacteria composite carbon (SCC) was easily synthesized, and the adsorption process of Cu(II) and Cr(VI) by SCC was examined. SCC-700-2-50% exhibited a high SBET (1047.54 m2/g) and developed pore structure rich in functional groups (such as -NH, -OH, and C-O). The combination of pore structure and functional groups improved the adsorption performance of SCC. The adsorption processes exhibited a synergistic effect in a binary system: the qm of Cu(II) and Cr(VI) were 386 mg/g and 341 mg/g, respectively, and the selectivity of Cu(II) adsorption by SCC was greater than Cr(VI). The adsorption process, examined by SEM-EDS, FTIR, and XPS analysis, indicated that Cu(II) as a cationic interface strengthens Cr(VI) adsorption through electrostatic interaction, and the anion Cr(VI) created a valid electrostatic shield against the electrostatic repulsion between H+ and Cu(II), facilitating Cu(II) adsorption. SCC had great reusability: Cu(II) and Cr(VI) adsorption capacity were 90% and 84%, of the initial adsorption capacity, respectively, after six cycles. This study demonstrates the prospect of SCC as a valid adsorbent for multiple heavy metal contaminations removal.

Enhance pore structure of cyanobacteria-based porous carbon by polypropylene to improve adsorption capacity of methylene blue.

Porous carbon obtained by co-pyrolysis of plastic and biomass has received a lot of attention due to its excellent adsorption properties, and the pore structure plays an essential role in adsorption performance, however, the pore structure is still not well understood. Herein, we synthesized cyanobacteria-based porous carbon derived from cyanobacteria and polypropylene plastic by one-step method. CPC-800-30% exhibited a high BET surface area (2140 m2/g), pore volume up to 1.44 cm3/g. PP not only improved the pore structure of porous carbon, but also enriched the types of functional groups, such as O-H, N-H, C=O, and -CH, due to dehydroxylation or amino group decreased, resulting in the hydrogen radicals increased, hence PP had positive effect for biomass during co-pyrolysis. Meanwhile, CPC-800-30% showed excellent methylene blue (MB) adsorption capacity (667 mg/g). This work provided a new strategy for enhancing porous carbon structure via using PP as additive.

3,9-Dichloro-2,4,8,10-tetra-oxa-3,9-di-phosphaspiro-[5.5]undecane-3,9-dione.

In the title compound, C(5)H(8)Cl(2)O(6)P(2), the two six-membered rings display chair conformations. The P=O bond distances are 1.444 (2) and 1.446 (2) Å. Weak inter-molecular C-H⋯O hydrogen bonds are present in the crystal structure.