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Contamination with energetic compounds (ECs) is common in military sites and poses a great risk to the environment and human health. However, its effects on the soil bacterial communities remain unclear. This study assessed the variations of bacterial communities, co-occurrence patterns, and their influence factors in three types of typical military-contaminated sites (artillery range, military-industrial site, and ammunition destruction site). The results showed that the most polluted sites were ammunition destruction sites, followed by military-industrial sites, whereas pollution in the artillery ranges was minimal. The average concentrations of ECs including 2,4,6-trinitrotoluene (TNT), hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), and octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) in the study sites ranged 120-1.67 × 10

Vanadium (V) contamination of soils poses potential risks to humans and ecosystems. This study was conducted to evaluate the effects of endophyte-assisted phytoremediation and to determine the mechanisms involved in V detoxification and plant growth promotion. Results showed that the endophytic bacterium Serratia marcescens PRE01 could successfully colonize the roots and increase the total V uptake of Pteris vittata by 25.4 %, with higher plant biomass and V accumulation in roots. Endophyte inoculation significantly improved the secretion of phytic, malic, and oxalic acids and accelerated FeVO

Cadmium (Cd) contamination in rice grains has become a severe issue worldwide. This study aims to explore feasible technologies applicable to different risk lands and develop a practical solution for safe rice production at a regional scale. Despite inconsistent field conditions in the whole region, various foliar fertilizers could effectively decrease grain Cd content by 20.4-41.6 % and were capable of producing safe grains in low/medium-risk areas. At high-risk sites, foliage dressing coupled with alkaline fertilizers significantly reduced Cd accumulation and increased grain compliance rate to 95.0 %. The cost analysis and questionnaire survey showed the above technologies are low-cost, eco-friendly, and highly acceptable in real-world scenarios. The classification results by conditional inference tree (CIT) for CK and FS scenarios indicated grain Cd content is closely related to the interaction effects of soil Cd and pH. On these bases, the whole area was divided spatially into three different risk zones, and each zone matched a feasible method for safe production, subsequently developing a precise and differentiated solution. The estimation results demonstrate it can effectively improve the precision level of safe utilization of regional polluted lands and save more than half of the total cost, providing a new idea for regional Cd-polluted paddy fields management strategies.

Iron materials have shown great potential to remediate arsenic (As) contaminated sites. It's very important to reveal the reaction process between iron materials and As from the perspective of pore scale, but relevant research was inadequate. In order to directly investigate the migration and As adsorption mechanism of starch-modified Fe-Ce oxide in pore scale, a silicon-based micromodel observation platform was established in this study. The results of Charge coupled Device images showed that the sedimentation surface area of SFC occupied about 57.02% of the large porosity zone, but only 23.27% of the small porosity zone. To further reveal the 3D distribution of Fe and As elements inside the pore network, Laser-Induced Breakdown Spectroscopy was introduced. The results revealed that less As was adsorbed as less SFC intruded in the small porosity zone. When the large porosity zone was blocked by SFC, a permeability barrier was created to adsorb As from upstream. This study also explored the effect of particle size reduction on SFC migration, and found it might be a better candidate for more SFC penetrated into small porosity zone. Combined with various high-resolution and sensitivity-detection methodologies, more colloidal migration mechanisms can be investigated using this technology in the future.

Heavy metal (HM) pollution of farmland is a serious problem worldwide and consumption of HM-contaminated food products poses significant public health risks. Phytoexclusion using low HM accumulating cultivars (LACs) is a promising and practical technology to mitigate the risk of HM contamination of agricultural products grown in polluted soils, and does not alter cultivation practices, is easy to apply, and is economical. This review provides an overview of the major scientific advances accomplished in the field of LACs worldwide. The LACs concept and identification criteria are presented, and the known LACs among currently cultivated grain crops and vegetables are re-evaluated. The low HM accumulation by LACs is affected by crop ecophysiological features and soil physicochemical characteristics. Taking low Cd accumulating cultivars as an example, it is known that they can efficiently exclude Cd from entering their edible parts in three ways: 1) decrease in root Cd uptake by reducing organic acids secretion in the rhizosphere and transport protein production; 2) restriction of Cd translocation from roots to shoots via enhanced Cd retention in the cell wall and Cd sequestration in vacuoles; and 3) reduction in Cd translocation from shoots to grains by limiting Cd redirection and remobilization mediated through nodes. We propose an LAC application strategy focused on LACs and optimized to work with other agronomic measures according to the classification of HM risk level for LACs, providing a cost-effective and practical solution for safe utilization of large areas of farmland polluted with low to moderate levels of HMs.

Microemulsion (ME) is considered as a stable solution for adsorbing organic matters. Aiming to remediate PAH contaminated soils from industrial sites in Shijiazhuang (Soil CPS) and Beijing (Soil CSG) in China, novel MEs were designed with different ratios of mixed surfactants (Surf, TX-100+Tween 80), n-butanol and fatty acid methyl esters (FAMEs). Particle size, transmittance, surface intension, Fourier transform infrared spectroscopy (FT-IR) and Raman spectroscopy of the MEs were analyzed. PAH removals by solubilization experiments were studied and regeneration of waste ME was evaluated. Results showed the novel MEs were obtained with particle sizes in a range of 18.53–122.77 nm. The lowest surface intension of MEs was 26.53 mN/m, which was prone to PAHs transferring to MEs. ‒OH (3350 cm-1), ‒C˭C (1740 cm-1) and ‒C‒O (1072 cm-1) functioned in forming MEs. Additionally, ‒OH, C‒H, ‒C˭C, ‒C‒O were considered as active binding sites when remediating PAH soils. PAH removals in soils CPS and CSG were up to 90.1% and 89.7% with surfactants and co-surfactant (Surf:Co-s), (Surf:Co-s) and FAME, soil and MEs (w:v) at ratios of 1:1, 8:2 and 1:4, respectively. About 85.6% of FAME and 41.9% of TX-100 in waste ME were recovered for recycle purpose.

The influence of persulfate activation methods on polycyclic aromatic hydrocarbons (PAHs) degradation was investigated and included thermal, citrate chelated iron, and alkaline, and a hydrogen peroxide (H₂O₂)-persulfate binary mixture. Thermal activation (60 °C) resulted in the highest removal of PAHs (99.1%) and persulfate consumption during thermal activation varied (0.45-1.38 g/kg soil). Persulfate consumption (0.91-1.22 g/kg soil) and PAHs removal (73.3-82.9%) varied using citrate chelated iron. No significant differences in oxidant consumption and PAH removal was measured in the H₂O₂-persulfate binary mixture and alkaline activated treatment systems, relative to the unactivated control. Greater removal of high molecular weight PAHs was measured with persulfate activation. Electron spin resonance spectra indicated the presence of hydroxyl radicals in thermally activated systems; weak hydroxyl radical activity in the H₂O₂-persulfate system; and superoxide radicals were predominant in alkaline activated systems. Differences in oxidative ability of the activated persulfate were related to different radicals generated during activation.

Bench-scale experiments were conducted to investigate the potassium permanganate demand, a key parameter for in situ chemical oxidation (ISCO) system design, and its variation with depth in PAHs-contaminated site of a coking plant. The concentrations of permanganate decreased rapidly during the first 8 d of the reaction process. The reaction follows first order kinetics, with rate constant ranging from 0.01 to 0.3/h. The total oxidant demand (TOD) is significantly higher for clayey silt fill than for soils of other lithology. The typical TOD is about 50 g MnO(4)(-)/kg soil for clayey silt fill, 20-40g MnO(4)(-)/kg soil for silt, silty clay and 1-7 g MnO(4)(-)/kg soil for fine sand. Statistical analysis revealed that TOD was positively correlated with total organic carbon (TOC) content, clay content and PAHs concentrations, besides sand content, meanwhile TOC was the parameter with the strongest influence on oxidant demand. After 32 d duration of oxidation, PAHs in all tested soils were effectively removed, with total removal percent ranging from 78% to 99%, and small molecular weight PAHs were removed to a greater extent than high molecular weight PAHs. Parameters obtained in this study, combined with soil bulk density, soil porosity and soil moisture, can be used for full-scale ISCO system design and application in coking contaminated site. (C) 2011 Elsevier B.V. All rights reserved.

The extent of PAH transformation, the formation and transformation of reaction byproducts during persulfate oxidation of polycyclic aromatic hydrocarbons (PAHs) in coking plant soil was investigated. Pre-oxidation analyses indicated that oxygen-containing PAHs (oxy-PAHs) existed in the soil. Oxy-PAHs including 1H-phenalen-1-one, 9H-fluoren-9-one, and 1,8-naphthalic anhydride were also produced during persulfate oxidation of PAHs. Concentration of 1,8-naphthalic anhydride at 4h in thermally activated (50 degrees C) persulfate oxidation (TAPO) treatment increased 12.7 times relative to the oxidant-free control. Additionally, the oxy-PAHs originally present and those generated during oxidation can be oxidized by unactivated or thermally activated persulfate oxidation. For example, 9H-fluoren-9-one concentration decreased 99% at 4 h in TAPO treatment relative to the control. Thermally activated persulfate resulted in greater oxy-PAHs removal than unactivated persulfate. Overall, both unactivated and thermally activated persulfate oxidation of PAH-contaminated soil reduced PAH mass, and oxidized most of the reaction byproducts. Consequently, this treatment process could limit environmental risk related to the parent compound and associated reaction byproducts. (C) 2014 Elsevier B.V. All rights reserved.