The determining factors of sediment nutrient content and stoichiometry along profile depth in seasonal water.

In the recent decades, the area of seasonal water (SEW) has substantially increased at the global scale. To evaluate nutrient dynamics in aquatic ecosystems, previous studies have analyzed the determining factors of sediment nutrient content and stoichiometry on whole sediment profiles without depth separation on SEW sites. Such a methodology assumes that SEW sediment is a uniform unit and its nutrient dynamics are regulated by the same mechanism at various depths (uniformity assumption). We tested this assumption using sediment samples from six depth increments of 154 sediment profiles (1 m depth) on SEW sites at Shengjin Lake in subtropical China. We measured sediment total nitrogen (STN), total phosphorus (STP), nutrient fractions, and the molar ratio of STN to STP (RSNP), and investigated their determining factors at various depths. STN, STP, and RSNP were averaged at 1.34 g/kg, 0.55 g/kg, and 5.43, respectively, and all gradually decreased with depth. STN was positively affected by moisture and flooding duration in all depth increments. Instead, the major determining factors of STP changed from particle size at 0-20 cm of depth to pH and electrical conductivity at 30-100 cm of depth. These vertical patterns have close connections with sediment nutrient fractions since sediment N fractions did not shift along profile depths (i.e., over 99 % of STN was organic N) but sediment P fractions did (the percentage of Fe-P and Al-P decreased by 6.25 % but those of Ca-P increased by 4.31 % along the sediment depth gradient). The major determining factors of RSNP showed no obvious vertical patterns because they frequently varied along depth gradients. The results demonstrate that SEW sediment is not a uniform unit and the determining factors of nutrient dynamics change with depth. Our study highlights the importance of improved methodological reflection in studies addressing sediment nutrient dynamics on SEW sites.

Impacts of land uses on spatio-temporal variations of seasonal water quality in a regulated river basin, Huai River, China.

Land use impacts from agriculture, industrialization, and human population should be considered in surface water quality management. In this study, we utilized an integrated statistical analysis approach mainly including a seasonal Mann-Kendall test, clustering analysis, self-organizing map, Boruta algorithm, and positive matrix factorization to the assessment of the interactions between land use types and water quality in a typical catchment in the Huai River Basin, China, over seven years (2012-2019). Spatially, water quality was clustered into three groups: upstream, midstream, and downstream/mainstream areas. The water quality of upstream sites was better than of mid-, down-, and mainstream. Temporally, water quality did not change significantly during the study period. However, the temporal variation in water quality of up-, down-, and mainstream areas was more stable than in the midstream. The interactions between land use types and water quality parameters at the sub-basin scale varied with seasons. Increasing forest/grassland areas could substantially improve the water quality during the wet season, while nutrients such as phosphorus from cropland and developed land was a driver for water quality deterioration in the dry season. Water area was not a significant factor influencing the variations of ammonia nitrogen (NH3-N) and total phosphorus (TP) in the wet or dry season, due to the intensive dams and sluices in study area. The parameters TP, and total nitrogen (TN) were principally linked with agricultural sources in the wet and dry seasons. The parameters NH3-N in the dry season, and chemical oxygen demand (CODCr) in the wet season were mainly associated with point source discharges. Agricultural source, and urban point source discharges were the main causes of water quality deterioration in the study area. Collectively, these results highlighted the impacts of land use types on variations of water quality parameters in the regulated basin.

Iron-modified phosphorus- and silicon-based biochars exhibited various influences on arsenic, cadmium, and lead accumulation in rice and enzyme activities in a paddy soil.

Contamination of paddy soils with potentially toxic elements (PTEs) has become a severe environmental issue. Application of functionalized biochar for rice cultivation has been proposed as an effective means to reduce environmental risks of these PTEs in paddy soils. This work was undertaken to seek the positive effects of a rice husk-derived silicon (Si)-rich biochar (Si-BC) and a pig carcass-derived phosphorus (P)-rich biochar (P-BC), as well as their Fe-modified biochars (Fe-Si-BC and Fe-P-BC) on the enzyme activity and PTE availability in an As-Cd-Pb-contaminated soil. A rice cultivation pot trial was conducted using these functionalized biochars as soil amendments for the alleviation of PTE accumulation in rice plants. Results showed that Si-BC decreased the concentrations of As in rice grain and straw by 59.4 % and 61.4 %, respectively, while Fe-Si-BC significantly (P < 0.05) enhanced plant growth, increasing grain yield (by 38.6 %). Fe-Si-BC significantly (P < 0.05) elevated Cd and Pb accumulation in rice plants. P-BC enhanced the activities of dehydrogenase, catalase, and urease, and reduced grain-Pb and straw-Pb by 49.3 % and 43.2 %, respectively. However, Fe-P-BC reduced plant-As in rice grain and straw by 12.2 % and 51.2 %, respectively, but increased plant-Cd and plant-Pb. Thus, Fe-modified Si- and P-rich biochars could remediate paddy soils contaminated with As, and enhance the yield and quality of rice. Application of pristine P-rich biochar could also be a promising strategy to remediate the Pb-contaminated paddy soils and limit Pb accumulation in rice.

Adsorption of potentially harmful elements by metal-biochar prepared via Co-pyrolysis of coffee grounds and Nano Fe(III) oxides.

Nano Fe(III) oxide (FO) was used as an amendment material in CO2-assisted pyrolysis of spent coffee grounds (SCG) and its impacts on the syngas (H2 & CO) generation and biochar adsorptive properties were investigated. Amendment of FO led to 153 and 682% increase of H2 and CO in pyrolytic process of SCG, respectively, which is deemed to arise from enhanced thermal cracking of hydrocarbons and oxygen transfer reaction mediated by FO. Incorporation of FO successfully created porous structure in the produced biochar. The adsorption tests revealed that the biochar exhibited bi-functional capability to remove both positively charged Cd(II) and Ni(II), and negatively charged Sb(V). The adsorption of Cd(II) and Ni(II) was hardly deteriorated in the multiple adsorption cycles, and the adsorption of Sb(V) was further enhanced through formation of surface ternary complexes. The overall results demonstrated nano Fe(III) oxide is a promising amendment material in CO2-assisted pyrolysis of lignocellulosic biomass for enhancing syngas generation and producing functional biochar.

Mechanisms and influencing factors of yttrium sorption on paddy soil: Experiments and modeling.

High-technology rare earth elements (REEs) as emerging contaminants have potentially hazardous risks for human health and the environment. Investigating the sorption of REEs on soils is crucial for understanding their migration and transformation. This study evaluated the sorption mechanisms and influencing factors of the rare earth element yttrium (Y) on paddy soil via integrated batch sorption experiments and theoretical modeling analysis. Site energy distribution theory (SEDT) combined with kinetics, thermodynamics, and isotherm sorption models were applied to illustrate the sorption mechanism. In addition, the effects of phosphorus (P), solution pH, particle size of soil microaggregates, and initial Y content on the sorption processes were evaluated by self-organizing map (SOM) and Boruta algorithm. The sorption kinetic behavior of Y on paddy soil was more consistent with the pseudo-second-order model. Thermodynamic results showed that the Y sorption was a spontaneous endothermic reaction. The generalized Langmuir model well described the isotherm data of Y sorption on heterogeneous paddy soil and soil microaggregates surface. The maximum sorption capacity of Y decreased with increasing soil particle size, which may be related to the number of sorption sites for Y on paddy soil and soil microaggregates, as confirmed by SEDT. The heterogeneity of sorption site energy for Y was the highest in the original paddy soil compared with the separated soil microaggregates. The SOM technique and Boruta algorithm highlighted that the initial concentration of Y and coexisting phosphorus played essential roles in the sorption process of Y, indicating that the addition of phosphate fertilizer may be an effective way to reduce the Y bioavailability in paddy soil in practice. These results can provide a scientific basis for the sustainable management of soil REEs and a theoretical foundation for the remediation of REEs-contaminated soils.

A review on functional polymer-clay based nanocomposite membranes for treatment of water.

Water is essential for every living being. Increasing population, mismanagement of water sources, urbanization, industrialization, globalization, and global warming have all contributed to the scarcity of fresh water sources and the growing demand of such resources. Securing and allocating sufficient water resources has thus become one of the current major global challenges. Membrane technology has dominated the field of water purification due to its ease of usage and fabrication with high efficiency. The development of novel membrane materials can hence play a central role in advancing the field of membrane technology. It is noted that polymer-clay nanocomposites have been used widely for treatment of waste water. Nonetheless, not much efforts have been put to functionalize their membranes to be selective for specific targets. This review was organized to offer better insights into various types of functional polymer and clays composite membranes developed for efficient treatment and purification of water/wastewater. Our discussion was extended further to evaluate the efficacy of membrane techniques employed in the water industry against major chemical (e.g., heavy metal, dye, and phenol) and biological contaminants (e.g., biofouling).

Thermochemical conversion of cobalt-loaded spent coffee grounds for production of energy resource and environmental catalyst.

Thermochemical conversion of cobalt (Co)-loaded lignin-rich spent coffee grounds (COSCG) was carried out to find the appropriate pyrolytic conditions (atmospheric gas and pyrolytic time) for syngas production (H2 and CO) and fabricate Co-biochar catalyst (CBC) in one step. The use of CO2 as atmospheric gas and 110-min pyrolytic time was optimal for generation of H2 (∼1.6 mol% in non-isothermal pyrolysis for 50 min) and CO (∼4.7 mol% in isothermal pyrolysis for 60 min) during thermochemical process of COSCG. The physicochemical properties of CBC fabricated using optimized pyrolytic conditions for syngas production were scrutinized using various analytical instruments (FE-SEM, TEM, XRD, and XPS). The characterizations exhibited that the catalyst consisted of metallic Co and surface wrinkled carbon layers. As a case study, the catalytic capability of CBC was tested by reducing p-nitrophenol (PNP), and the reaction kinetics of PNP in the presence of CBC was measured from 0.04 to 0.12 s-1.

Fabrication of magnetic biochar as a treatment medium for As(V) via pyrolysis of FeCl3-pretreated spent coffee ground.

This study investigated the preparation of magnetic biochar from N2- and CO2-assisted pyrolysis of spent coffee ground (SCG) for use as an adsorption medium for As(V), and the effects of FeCl3 pretreatment of SCG on the material properties and adsorption capability of the produced biochar. Pyrolysis of FeCl3-pretreated SCG in CO2 atmosphere produced highly porous biochar with its surface area ∼70 times greater than that produced in N2 condition. However, despite the small surface area, biochar produced in N2 showed greater As(V) adsorption capability. X-ray diffraction and X-ray photoelectron spectrometer analyses identified Fe3C and Fe3O4 as dominant mineral phases in N2 and CO2 conditions, with the former being much more adsorptive toward As(V). The overall results suggest functional biochar can be facilely fabricated by necessary pretreatment to expand the applicability of biochar for specific purposes.

Carbon dioxide assisted sustainability enhancement of pyrolysis of waste biomass: A case study with spent coffee ground.

This work mainly presents the influence of CO2 as a reaction medium in the thermo-chemical process (pyrolysis) of waste biomass. Our experimental work mechanistically validated two key roles of CO2 in pyrolysis of biomass. For example, CO2 expedited the thermal cracking of volatile organic compounds (VOCs) evolved from the thermal degradation of spent coffee ground (SCG) and reacted with VOCs. This enhanced thermal cracking behavior and reaction triggered by CO2 directly led to the enhanced generation of CO (∼ 3000%) in the presence of CO2. As a result, this identified influence of CO2 also directly led to the substantial decrease (∼ 40-60%) of the condensable hydrocarbons (tar). Finally, the morphologic change of biochar was distinctive in the presence of CO2. Therefore, a series of the adsorption experiments with dye were conducted to preliminary explore the physico-chemical properties of biochar induced by CO2.

Pilot-scale passive bioreactors for the treatment of acid mine drainage: efficiency of mushroom compost vs. mixed substrates for metal removal.

Pilot-scale field-testing of passive bioreactors was performed to evaluate the efficiency of a mixture of four substrates (cow manure compost, mushroom compost, sawdust, and rice straw) relative to mushroom compost alone, and of the effect of the Fe/Mn ratio, during the treatment of acid mine drainage (AMD) over a 174-day period. Three 141 L columns, filled with either mushroom compost or the four substrate mixture (in duplicate), were set-up and fed with AMD from a closed mine site, in South Korea, using a 4-day hydraulic retention time. In the former bioreactor, effluent deterioration was observed over 1-2 months, despite the good efficiency predicted by the physicochemical characterization of mushroom compost. Steady state effluent quality was then noted for around 100 days before worsening in AMD source water occurred in response to seasonal variations in precipitation. Such changes in AMD quality resulted in performance deterioration in all reactors followed by a slow recovery toward the end of testing. Both substrates (mushroom compost and mixtures) gave satisfactory performance in neutralizing pH (6.1-7.8). Moreover, the system was able to consistently reduce sulfate from day 49, after the initial leaching out from organic substrates. Metal removal efficiencies were on the order of Al (∼100%) > Fe (68-92%) > Mn (49-61%). Overall, the mixed substrates showed comparable performance to mushroom compost, while yielding better effluent quality upon start-up. The results also indicated mushroom compost could release significant amounts of Mn and sulfate during bioreactor operation.

Comparative effectiveness of mixed organic substrates to mushroom compost for treatment of mine drainage in passive bioreactors.

Bioreactors are one possible best sustainable technology to address the mine-impacted water problems. Several prospective substrates (mushroom compost, cow manure, sawdust, wood chips, and cut rice straw) were characterized for their ability to serve as a source of food and energy for sulfate-reducing bacteria. Twenty bench-scale batch bioreactors were then designed and set up to investigate relative effectiveness of various mixtures of substrates to that of mushroom compost, the most commonly used substrate in field bioreactors, for treating mine drainage with acidic (pH 3) and moderate pH (pH 6). Overall, reactive mixtures showed satisfactory performances in generating alkalinity, reducing sulfate and removing metals (Al>Fe>Mn) (up to 100%) at both pH conditions, for all substrates. The mixture of sawdust and cow manure was found as the most effective whereas the mixture containing 40% cut rice straw gave limited efficiency, suggesting organic carbon released from this substrate is not readily available for biodegradation under anaerobic conditions. The mushroom compost-based bioreactors released significant amount of sulfate, which may raise a more concern upon the start-up of field-scale bioreactors. The correlation between the extent of sulfate reduction and dissolved organic carbon/SO(4)(2-) ratio was weak and this indicates that the type of dissolved organic carbon plays a more important role in sulfate reduction than the absolute concentration and that the ratio is not sensitive enough to properly describe the relative effectiveness of substrate mixtures.