Sorghum-Waste-Derived High-Surface Area KOH-Activated Porous Carbon for Highly Efficient Methylene Blue and Pb(II) Removal.

With the development of the environment and human society, the removal of metal ions and dyes in wastewater treatment remains an urgent problem to solve. In this work, two biomass carbon adsorbents were synthesized by a KOH activation and carbonization route using sorghum stem and root as carbon precursors. In comparison with the samples without KOH activation, the pore structure of the KOH-activated carbon has been dramatically improved. The findings show that the specific surface areas of the adsorbents by sorghum stem (S1) and sorghum root (R1) were 948.6 and 168.1 m2 g-1, respectively. Meanwhile, the abundant OH- and COO- groups on the surface of these adsorbents endow them with negative polarity, thereby exhibiting excellent adsorption performance for removing methylene blue (MB) and Pb(II) from wastewater. The adsorption amount and removal rate of S1 were 98.1 mg g-1 and 98.08%, respectively, for MB, whereas those of R1 were 197.6 mg g-1 and 98.82% for the Pb(II) ion, respectively. Our findings offer an invaluable insight into designing and synthesizing a highly efficient sustainable adsorbent to remove MB and Pb(II) based on biomass agricultural waste.

Spatiotemporal variations of biogenic elements and sources of sedimentary organic matter in the largest oyster mariculture bay (Maowei Sea), Southwest China.

China is the largest mariculture producer in the world, but detailed information on the spatiotemporal variations of biogenic elements and sources of sedimentary organic matter (SOM) via mariculture is limited. The primary objective of this study was to assess the influence of mariculture on the origin of SOM in relation with biogenic elements and geochemical paramaters due to the importance of SOM as a potential source of nutrients and energy in coastal marine environments. Surface sediments from the Maowei Sea were collected in August (summer) and December (winter), 2016 for grain size, total organic carbon (TOC), total nitrogen (TN), organic phosphorus (OP), biogenic silica (BSi), δ13C and δ15N analyses. Significant correlation (p < 0.01) was observed between TOC and TN in summer and winter respectively, indicating that they have common source in both seasons. The spatiotemporal distributions of TOC, TN, OP and BSi were influenced by the sources and distribution of SOM, grain sizes and hydrodynamic conditions in the Maowei Sea. The overall ranges of δ13C (-26.86‰ to -23.01‰) and δ15N (2.54‰ to 9.82‰) and C/N ratio (5.83 to 18.67) showed that SOM is derived from mixed sources. The δ13C and δ15N-based three-end-member mixing model results revealed that >40% of the deposited SOM originates from terrestrial source during two seasons. The SOM from shellfish mariculture was seasonal, mainly deposited in the intensive mariculture areas, and its proportions were only higher than contributions from marine plankton in summer. Generally, this study indicates that shellfish biodepositions can significantly influence the cycle of carbon and other biogenic elements in the intensive mariculture areas. Nevertheless, the overall dominance of terrestrial and marine SOM suggests that the sources of SOM and factors influencing carbon cycling in the Maowei Sea do not exclusively depend on the intensity of mariculture activities.

Distribution characteristics and ecological evaluation of chlorobenzene compounds in surface sediment of the Maowei Sea, Guangxi, China.

To enhance our understanding on environmental conditions of the Maowei Sea in Guangxi province, China, the concentration and distribution of 22 chlorobenzene compounds (CBs) in the surface sediment were determined by gas chromatography-mass spectrometry (GC-MS). The relationship of the sediment between CBs and total organic carbon (TOC) was also investigated. The results showed that a total of eight kinds of CBs compounds were detected in the sediment samples which were collected from the coastal environment of the Maowei Sea, with an average concentration of 15.3 ng·g-1 (the concentration range, 2.5-61.5 ng·g-1). The rank of their average concentrations was as follows: 2,3,4,5,6-pentachlorotoluene > hexachlorobenzene, 2-chlorotoluene, 3-chlorotoluene and 2,3-dichlorotoluene > 2,4-dichlorotoluene > 4-chlorotoluene > pentachlorobenzene. Most CBs were distributed in sediments along the east coast of the Maowei Sea. For total TOC content in sediments, the concentration in the sampling locations was similar, with a mean concentration of 8.83 g·kg-1 (the concentration range, 4.87-20.13 g·kg-1). However, there was no significant correlation between the concentration of TOC and total CBs. Compared to the corresponding CBs in the sediment of other coastal areas in mainland China and other countries, the value of CBs in the Maowei Sea was low.

Chlorinated polycyclic aromatic hydrocarbons in surface sediment from Maowei Sea, Guangxi, China: occurrence, distribution, and source apportionment.

Chlorinated polycyclic aromatic hydrocarbons (ClPAHs) with three to five aromatic rings have been documented to ubiquitously occur in environmental matrices. In this study, residual concentrations and profiles of 20 individual ClPAHs were determined in 35 surface sediment samples from Maowei Sea, a semi-enclosed shallow inland bay located in the northwestern part of South China Sea. The concentrations of ΣClPAHs in sediment ranged from 313 to 9650 pg/g dw with a detection rate of 43-100%. Of the individual ClPAH congeners, 9-ClPhe was the most abundant in Maowei Sea with the concentrations that ranged from 99.9 to 3610 pg/g dw (mean 1120 pg/g dw). High-molecular-weight ClPAH congeners (four to five rings) were predominant in sediments from sampling locations near a petrochemical industrial complex, whereas low-molecular-weight ClPAH congeners (three rings) were predominant in sediments from estuarine and mangrove locations. A positive matrix factorization (PMF) model in combination with dioxin-like toxic equivalency quotient (TEQ) results was used to apportion sources of ClPAHs. Vehicular emission, combustion/chemical industrial processes, and two other unknown sources accounted for 40.1, 25.5, 20.8, and 13.6%, respectively, of ClPAH sources in sediment; their contribution to TEQs in sediments were 24.2, 40.5, 19.3, and 16.0%, respectively. Further investigations are needed to elucidate potential sources and ecological risks of ClPAHs in sediments.