A highly porous animal bone-derived char with a superiority of promoting nZVI for Cr(VI) sequestration in agricultural soils

Paddy soil and irrigation water are commonly contaminated with hexavalent chromium [Cr(VI)] near urban industrial areas, thereby threatening the safety of agricultural products and human health. In this study, we develop a porous and high specific area bone char (BC) to support nanoscale zero-valent iron (nZVI) and apply it to remediate Cr(VI) pollution in water and paddy soil under anaerobic conditions. The batch experiments reveal that BC/nZVI exhibits a higher removal capacity of 516.7 mg/(g?nZVI) for Cr(VI) than nZVI when normalized to the actual nZVI content, which is 2.8 times that of nZVI; moreover, the highest nZVI utilization is the nZVI loading of 15% (BC/nZVI15). The Cr(VI) removal efficiency of BC/nZVI15 decreases with increasing pH (4 – 10). Coexisting ions (phosphate and carbonate) and humic acid can inhibit the removal of Cr(VI) with BC/nZVI15. Additionally, BC exhibits a strong advantage in promoting Cr(VI) removal by nZVI compared to the widely used biochar and activated carbon. Our results demonstrate that reduction and coprecipitation are the dominant Cr(VI) removal mechanisms. Furthermore, BC/nZVI15 shows a significantly higher reduction and removal efficiency as well as a strong anti-interference ability for Cr(VI) in paddy soil, as compared to nZVI. These findings provide a new effective material for remediating Cr(VI) pollution from water and soil.     

Physiological and biochemical characteristic of Miscanthus × giganteus grown in heavy metal – oil sludge co-contaminated soil

The effect of oil sludge and zinc, present in soil both separately and as a mixture on the physiological and biochemical parameters of Miscanthus × giganteus plant was examined in a pot experiment. The opposite effect of pollutants on the accumulation of plant biomass was established: in comparison with uncontaminated control the oil sludge increased, and Zn reduced the root and shoot biomass. Oil sludge had an inhibitory effect on the plant photosynthetic apparatus, which intensified in the presence of Zn. The specific antioxidant response of M. × giganteus to the presence of both pollutants was a marked increase in the activity of superoxide dismutase (mostly owing to oil sludge) and glutathione-S-transferase (mostly owing to zinc) in the shoots. The participation of glutathione-S-transferase in the detoxification of both the organic and the inorganic pollutants was assumed. Zn inhibited the activity of laccase-like oxidase, whereas oil sludge promoted laccase and ascorbate oxidase activities. This finding suggests that these enzymes play a part in the oxidative detoxification of the organic pollutаnt. With both pollutants used jointly, Zn accumulation in the roots increased 6-fold, leading to increase in the efficiency of soil clean-up from the metal. In turn, Zn did not significantly affect the soil clean-up from oil sludge. This study shows for the first time the effect of co-contamination of soil with oil sludge and Zn on the physiological and biochemical characteristics of the bioenergetic plant M. × giganteus. The data obtained are important for understanding the mechanisms of phytoremediation with this plant.     

How do inundation provoke the release of phosphorus in soil-originated sediment due to nitrogen reduction after reclaiming lake from polder

Different N and P fractions in microcosm incubation experiment was measured using high-resolution in-situ Peeper and DGT techniques combining with sequential extraction procedure. The results showed the synchronous desorption and release of PO₄^3-, S^2- and Fe²⁺ from the solid soil-originated sediment. This trend indicated that the significant reduction of Fe-P and SO₄^2- occurred in the pore water during the inundation. The concentrations of PO₄^3- in the overlying water and pore water increased to more than 0.1 and 0.2 mg/L at the beginning of the incubation experiment. Decreased NO₃^-concentrations from more than 1.5 mg/L to less than 0.5 mg/L combining with increasing NH₄⁺ concentrations from less than 1 mg/L to more than 5 mg/L suggested the remarkable NO₃^- reduction via dissimilatory nitrate reduction to ammonia (DNRA) pathway over time. High NH₄⁺ concentrations in the pore water aggravated the release of Fe²⁺ through reduction of Fe(III)-P as electric acceptors under anaerobic conditions. This process further stimulated the remarkable releasing of labile PO₄^3- from the solid phase to the solution and potential diffusion into overlying water. Additionally, high S^2- concentration at deeper layer indicated the reduction and releasing of S^2- from oxidation states, which can stimulated the NO₃^- reduction and the accumulation of NH₄⁺ in the pore water. This process can also provoke the reduction of Fe-P as electric acceptors following the release of labile PO₄^3- into pore water. Generally, inundation potentially facilitate the desorption of labile P and attention should be paid during the reclaiming lake from polder.     

Impact assessment of climate policy on Poland's power sector

This article addresses the impact of the European Union Emissions Trading System (EU ETS) on Poland’s conventional energy sector in 2008–2020 and further till 2050. Poland is a country with over 80% dependence on coal in the power sector being under political pressure of the European Union’s (EU) ambitious climate policy. The impact of the increase of the European Emission Allowance (EUA) price on fossil fuel power sector has been modelled for different scenarios. The innovation of this article consists in proposing a methodology of estimation actual costs and benefits of power stations in a country with a heavily coal-dependent power sector in the process of transition to a low-carbon economy. Strong political and economic interdependence of coal and power sector has been demonstrated as well as the impact caused by the EU ETS participation in different technology groups of power plants. It has been shown that gas-fuelled combined heat and power units are less vulnerable to the EU ETS-related costs, whereas the hard coal-fired plants may lose their profitability soon after 2020. Lignite power plants, despite their high emissivity, may longer remain in operation owing to low operational costs. Additionally, the results of long-term, up to 2050, modelling of Poland’s energy sector supported an unavoidable need of deep decarbonisation of the power sector to meet the post-Paris climate objectives. It has been concluded that investing in coal-based power capacity may lead to a carbon lock-in of the power sector. Finally, the overall costs of such a transformation have been discussed and confronted with the financial support offered by the EU. The whole consideration has been made in a wide context of changes ongoing globally in energy markets and compared with some other countries seeking transformation paths from coal. Poland’s case can serve as a lesson for all countries trying to reduce coal dependence in power generation. Reforms in the energy sector shall from the very beginning be an essential part of a sustainable transition of the whole nation’s economy. They must scale the power capacity to the future demand avoiding stranded costs. The reforms must be wide-ranging, based on a wide political consensus and not biased against the coal sector. Future energy mix and corresponding technologies shall be carefully designed, matched and should remain stable in the long-term perspective. Coal-based power capacity being near the end of its lifetime provides an economically viable option to commence a fuel switch and the following technology replacement. Real benefits and costs of the energy transition shall be fairly allocated to all stakeholders and communicated to the society. The social costs and implications in coal-dependent regions may be high, especially in the short-term perspective, but then the transformation will bring profits to the whole society.     

Mitigation and adaptation strategies for global change via the implementation of underground coal gasification

Coal is the most abundant hydrocarbon energy source in the world. It also produces a very high volume of greenhouse gases using the current production technology. It is more difficult to handle and transport than crude oil and natural gas. We face a challenge: how can we access this abundant resource and at the same time mitigate global environmental challenges, in particular, the production of carbon dioxide (CO₂)? The editors of this special edition journal consider the opportunity to increase the utilization of this globally abundant resource and recover it in an environmentally sustainable manner. Underground coal gasification (UCG) is the recovery of energy from coal by gasifying the coal underground. This  process produces a high calorific synthesis gas, which can be applied for electricity generation and/or the production of fuels and chemicals. The carbon dioxide emissions are relatively pure and the surface facilities are limited in their environmental footprint. Unused carbon is readily separated and can be geo-sequester in the resulting cavity. The cavity is also being considered as a potential option to mitigate against change impacts of other sources of carbon dioxide (CO₂) emissions. These outcomes mean there is an opportunity to provide developing and developed countries a source of low-cost clean energy. Further, the burning of coal in situ means that the traditional dangers of underground mining and extraction are reduced, a higher percentage of the coal is actually recovered and the resulting cavern creates the potential for a long-term storage solution of the gasification wastes. The process is not without challenges. Ground subsidence and groundwater pollution are two potential environmental impacts that need to be averted for this process to be acceptable. It is essential to advance the understanding of this practice and this special edition journal seeks to share the progress that scientists are making in this dynamic field. The technical challenges are being addressed by researchers around the world who work to resolve and understand how burning coal underground impacts the geology, the surface land, and ground water both in the short and the long term. This special issue reviews the process of UCG and considers the opportunities, challenges, risks, competitive analysis and synergies, commercial initiatives and a roadmap to solutions via the modelling and simulation of UCG. Building and then disseminating the fundamental knowledge of UCG will enhance policy development, best practices and processes that reflect the global desires for energy production with reduced environmental impact.     

Magnetic compass orientation of migratory birds in the presence of a 1.315 MHz oscillating field

The radical pair model of magnetoreception predicts that magnetic compass orientation can be disrupted by high frequency magnetic fields in the Megahertz range. European robins, Erithacus rubecula, were tested under monochromatic 565 nm green light in 1.315 MHz fields of 0.48 T during spring and autumn migration, with 1.315 MHz being the frequency that matches the energetic splitting induced by the local geomagnetic field. The birds responses depended on the alignment of the oscillating field with respect to the static geomagnetic field: when the 1.315 MHz field was aligned parallel with the field lines, birds significantly preferred northerly directions in spring and southerly directions in autumn. These preferences reflect normal migratory orientation, with the variance slightly increased compared to control tests in the geomagnetic field alone or to tests in a 7.0 MHz field. However, in the 1.315 MHz field aligned at a 24° angle to the field lines, the birds were disoriented in both seasons, indicating that the high frequency field interfered with magnetoreception. These finding are in agreement with theoretical predictions and support the assumption of a radical-pair mechanism underlying the processes mediating magnetic compass information in birds.     

Long-term (≥20 years) application of fertilizers and straw return enhances soil carbon storage: a meta-analysis

Increasing soil carbon (C) storage is crucial to addressing climate change and ensuring food security. The C sequestration potential of the world’s cropland soil is 0.4–0.8 Pg soil C year^?1, which may be achieved through the adoption of recommended management practices (RMPs), including fertilizer management. This study aimed to quantitatively evaluate the influence of long-term application of different fertilizers and straw retention on soil organic carbon (SOC) storage, to compare the calculated response ratios with Intergovernmental Panel on Climate Change (IPCC)-recommended default relative stock change factors, and to propose recommendations for enhancing SOC sequestration. The meta-analysis indicated that the long-term application of chemical fertilizers (CF), organic fertilizers (OF), combined chemical and organic fertilizers (CFOF), and straw return (SR) significantly enhanced the SOC storage. Response ratios varied significantly (p < 0.05) across different fertilization measures and climatic zones, and was sensitive to the initial SOC content. The mean response ratio was 0.94 for no fertilizer (NF), 1.08 for CF, 1.48 for OF, 1.38 for CFOF, and 1.28 for SR. When IPCC default values for response ratios were applied, SOC storage with OF and CFOF treatments in warm temperate regions with a dry climate was underestimated by 26%, and in the cool temperate region with a moist climate was overestimated by 25% (p < 0.05). Analysis showed that sustained application of organic fertilizers and straw return could be a beneficial measures to mitigate climate change and ensure food security in China. Our findings highlight the importance of deriving SOC stock change factors for a detailed classification of cropland by fertilizer management, climate, and soil types in order to more accurately reflect the effects of policy measures.     

Effect of Cu loading content on the catalytic performance of Cu-USY catalysts for selective catalytic reduction of NO with NH3

Series of Cu-USY zeolite catalyst with different Cu loading content were synthesized through simple impregnation method. The obtained catalysts were subjected to selective catalytic reduction of NO_x with NH₃ (NH₃-SCR) performance evaluation, structural/chemical characterizations such as X-ray diffraction (XRD), N₂ adsorption/desorption, H₂ temperature-programmed reduction (H₂-TPR), NH₃ temperature-programmed desorption (NH₃-TPD) as well as detailed in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) experiments including CO adsorption, NH₃ adsorption and NO+O₂ in situ reactions. Results show that Cu-USY with proper Cu loading (in this work 5Cu-USY with 5 wt.% Cu) could be promising candidates with highly efficient NH₃-SCR catalytic performance, relatively low byproduct formation and excellent hydrothermal stability, although its SO₂ poisoning tolerability needs alleviation. Further characterizations reveal that such catalytic advantages can be attributed to both active cu species and surface acid centers evolution modulated by Cu loading. On one hand, Cu species in the super cages of zeolites increases with higher Cu content and being more conducive for NH₃-SCR reactivity. On the other hand, higher Cu loading leads to depletion of Brønsted acid centers and simultaneous formation of abundant Lewis acid centers, which facilitates NH₄NO₃ reduction via NH₃ adsorbed on Lewis acid centers, thus improving SCR reactivity. However, Cu over-introduction leads to formation of surface highly dispersed CuO_x, causing unfavorable NH₃ oxidation and inferior N₂ selectivity.     

High mercury leachate containing HgS22 − complex ion: Detoxifying solidification and high efficiency Hg extraction

Clean and efficient treatment of high-mercury leachate produced from remediation of mercury-polluted soil has become a huge challenge for environmental scientists.In this work,cement solidification was firstly adopted to treat the high-concentration mercury leachate,which had high alkalinity.Different mercury concentrations,namely 3.120 mg/L Hg mercury leachate and 9.243 mg/L Hg mercury concentrated leachate,were separately solidified by Portland cement.The results indicated that simply using the cement can properly solidify both the leachates to meet the waste landfill standard,with liquid(mL)/solid(g) ratio(L/S ratio) of4:10–6:10.In order to make full use of mercury in the leachates,a Hg extraction method was subsequently carried out under different experimental parameters,such as temperature and p H value.It was shown that the Hg extraction ratio could reach as high as 99.84% and almost all the mercury in the leachate could be transformed to HgS precipitate;moreover,the Hg concentration in the treated leachate was reduced from 3.120 to 0.005 mg/L at p H 2.98 and 30°C,which was much less than the limit of the national standard,indicating that the leachate had been completely cleaned and could be discharged freely.Hence,simple cement solidification renders high-mercury leachate nontoxic,and the Hg extraction method can successfully recover the Hg and enable the residual leachate to be discharged safely.     

Modified activated carbon with interconnected fibrils of iron-oxyhydroxides using Mn2 + as morphology regulator, for a superior arsenic removal from water

The arsenic removal efficiency of iron-modified activated carbons depends greatly on the number of available iron oxide surface sites, which are given by the surface area of the anchored particles. In this sense, aiming the generation of an adsorbent with superior arsenic adsorption capacity, we developed a protocol to anchor interconnected fibrils of iron oxyhydroxides, using Mn^2 + as a morphology regulator. The protocol was based on a microwave-assisted hydrothermal method, using bituminous based activated carbon and both Fe^2 + and Mn^2 + ions in the hydrolysis solution. The elemental analysis of modified carbons revealed that Mn does not anchor to the carbon. However, when Mn is included in the hydrolysis solution, the iron content in the activated carbon increased up to 3.5?wt%, without considerable decreasing the adsorbent surface area. Under specific hydrothermal conditions, the Mn^2 + promoted the formation of iron oxide nanoparticles shaped as interconnected fibrils. This material showed a superior arsenic adsorption capacity in comparison to similar iron modified activated carbons (5?mg As/g carbon, at 2?mg As/L), attributed to the increase in quantity and availability of active sites located on the novel interconnected fibrils of iron oxyhydroxides nanostructures.