Spatiotemporal changes in vegetation coverage and its causes in China since the Chinese economic reform Abstract With the rapid development of the economy over 40 years since the initiation of Chinese economic reform, terrestrial ecosystems in China have undergone large-scale changes. In this study, we investigated vegetation dynamics in China and their relationships with climatic factors and anthropogenic drivers over 15 progressive periods of 18–32 years starting in 1982. This was accomplished by using the third-generation global satellite Advanced Very High Resolution Radiometer (AVHRR), Normalized Difference Vegetation Index (NDVI) dataset, night-time satellite data, and climate data. Across China, NDVI increased significantly during 1982–2013; especially significant increases were observed in all periods during the growing season and spring. At the pixel scale, 21–38% of the vegetated area in the 15 periods experienced a significant positive trend in vegetation growth. This increase was mostly located in central and southern China. A significant negative trend was observed in 1–8% of the vegetated area pixels, and this pattern was mainly seen in northwestern China, the Yangtze River Delta region, and the Pearl River Delta region. The contribution of spring NDVI to vegetation improvement increased, while the contribution of summer NDVI decreased. Vegetation activity in China was mainly regulated by thermal factors, especially pronounced in mountainous regions of northern China. However, the restrictive effect of moisture factors was very marked to vegetation growth in areas with less than 400 mm of precipitation. Urbanization in China has led to vegetation degradation in most urban centers and surrounding areas in central and eastern China. The increase of agricultural plantations, the Grain for Green Project, and a series ecological restoration projects in some areas have promoted vegetation coverage.

Evaluation of orange peel-derived activated carbons for treatment of dye-contaminated wastewater tailings Abstract Dyes are colored compounds which are visible even at trace concentrations. Due to their recalcitrance and esthetic persistence, certain methods are unable to effectively eliminate them. So far, adsorptive treatment using activated carbons (ACs) is one of the most successful methods. In this study, we have employed orange peel (OP) as a cost-effective alternative to the expensive coal- and coir-based precursors to synthesize ACs for cationic methylene blue (MB) and anionic methyl orange (MO) dye adsorption. The pre-carbonized OP was activated via H2SO4, NaOH, KOH, ZnCl2, and H3PO4 to study the effects of activation reagents on dye removal efficiencies and mechanisms. Among several isotherm models employed to fit the adsorption data, the Langmuir and Sips models sufficiently estimated the maximum equilibrium uptakes close to the experimental values of 1012.10 ± 29.13, 339.82 ± 6.98, and 382.15 ± 8.62 mg/g, for ZnCl2-AC (MO), ZnCl2-AC (MB), and KOH-AC (MB), respectively. The adsorption mechanisms were suggested to involve electrostatic binding, pi–pi interactions, hydrogen bonding, and electron donor–acceptor reactions. Consequently, more than 99% removal efficiency was achieved from a laboratory organic wastewater sample bearing ~ 35 mg/L of MB. The results thus suggest that the synthesized ACs from agricultural waste have the tendencies to be applied to real dye wastewater treatment.

Long-term leaching characterization and geochemical modeling of chromium released from AOD slag Abstract The long-term leaching of chromium from AOD slag was analyzed by column percolation test (CEN/TS 14405). According to the analytical result, the eluate of the AOD slag exhibited alkaline and reductive property. Chromium released from the AOD slag was primarily presented as trivalent chromium (Cr(III)). The eluate exhibited low hexavalent chromium (Cr(VI)) concentration. As the L/S ratio increased to 115 L kg−1, the accumulated release quantity of Cr(III) and total chromium per AOD slag mass reached 1549.68 and 1613.67 μg kg−1, respectively. The long-term leaching toxicity of chromium from the AOD slag was noticeable. Besides, a long-term geochemical model was built with PHREEQC software to assess the evolution of pH and chromium concentration in the eluate. The simulated pH and chromium concentrations were well consistent with those of the column percolation experiment. The result suggested that the geochemical model for chromium leaching prediction applies to the assessment of the eco-risk of AOD slag during the long-term leaching. The concentration of trivalent chromium presenting as Cr(OH)4− for instability of Cr(III) hydroxide in the alkaline eluate was regulated by the dissolution of the primary phase Cr2O3.

Chronic sublethal effects of ZnO nanoparticles on Tigriopus fulvus (Copepoda, Harpacticoida) Abstract This study investigated for the first time the effects of ZnO nanoparticle (NP) chronic exposure (28 days) on Tigriopus fulvus. Acute toxicity (48 h) of three Zn chemical forms was assessed as well including the following: (a) ZnO nanoparticles (NPs), (b) Zn2+ from ZnO NP suspension after centrifugation (supernatant) and (c) ZnSO4 H2O. Physical-chemical and electronic microscopies were used to characterize spiked exposure media. Results showed that the dissolution of ZnO NPs was significant, with a complete dissolution at lowest test concentrations, but nano- and micro-aggregates were always present. Acute test evidenced a significant higher toxicity of Zn2+ and ZnSO4 compared to ZnO NPs. The chronic exposure to ZnO NPs caused negative effects on the reproductive traits, i.e. brood duration, brood size and brood number at much lower concentrations (≥ 100 μg/L). The appearance of ovigerous females was delayed at higher concentrations of ZnO NPs, while the time required for offspring release and the percentage of non-viable eggs per female were significantly increased. ZnO NP subchronic exposure evidenced its ability to reduce T. fulvus individual reproductive fitness, suggesting that ZnO NPs use and release must be carefully monitored. Graphical abstract Graphical Abstract.

Particulate matter emissions of less harmful-looking super-slim size cigarettes appealing to women: a laser spectrometric analysis of second-hand smoke Abstract Slim tobacco products shall appear by their look less harmful. In 2013, the European Union ministers discussed to ban them. However, only a ban on small package sizes was realized. To add more data for exposure risk assessment of slim tobacco products, the particulate matter (PM) amount in second-hand smoke (SHS) of super-slim size cigarettes compared with a king size brand was investigated. PM amount of four super-slim size cigarette types of the brand Couture was analysed in comparison with the king-size reference cigarette. Therefore, SHS was produced in an enclosed space with a volume of 2.88 m3 by an automatic environmental tobacco smoke emitter. PM size fractions PM10, PM2.5 and PM1 were measured in real time using a laser aerosol spectrometer. SHS of Couture Gold contained about 36% and Couture Purple about 28% more PM than the reference cigarette. In contrast, Couture Green emitted about 37% and Couture Silver about 53% less PM than the reference cigarette. Depending on the brand, the PM2.5 mean concentrations increased up to 1538 μg/m3. This exceeds the 24-h mean concentration of at most 25 μg/m3 according to the WHO Air quality guidelines about 62-fold. Smoking in enclosed rooms leads to a massive increase of PM. The PM pollution by slim-size tobacco products are substantial and sometimes higher than by king size tobacco products. Therefore, SHS exposure from slim-size tobacco products is not less harmful to health. Decision makers should take this aspect in consideration.

CeCu composite oxide for chlorophenol effective removal by heterogeneous catalytic wet peroxide oxidation Abstract CeCu solid solution oxide catalysts were prepared by the complex method and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET), and X-ray photoelectron spectroscopy (XPS). And its activity in the catalytic wet peroxide oxidation (CWPO) of 4-chlorophenol (4-CP) and 2,4-dichlorophenol (2,4-DCP) in water was investigated. The results showed that the Cu2+ ions dissolved into the CeO2 lattice to form CeCu solid solution oxide with a coarse, interconnected, porous, and cotton-like morphology. The metal-oxygen bonds were weakened by the formation of solid solution in the CeCu oxide catalyst. This weakening facilitated the activation and decomposition of the H2O2 to form highly oxidative HO· species that can lead to significant chlorophenol mineralization. The formation of CeCu solid solution oxide can effectively inhibit the Cu ions to be leached from the used CeCu oxide catalysts, which can ensure the CeCu oxide catalysts to adapt to a wide pH range of 2.1–7.9 and exhibit good reusability. CWPO reaction of 4-CP and 2,4-DCP molecules on CeCu oxide catalysts conforms to the first-order kinetic equation: y = 6959.3x − 17.2 and y = 9725x − 25.4, respectively. And the reaction activation energies are 57.8 and 80.8 kJ/mol, respectively. The TOC removals of 4-CP and 2,4-DCP can exceed 88 and 82%, and the dechlorination rates of 4-CP and 2,4-DCP are higher than 95 and 99.5%, respectively.

Magnetic hybrid gels for emulsified oil adsorption: an overview of their potential to solve environmental problems associated to petroleum spills Abstract Hydrogels (HGs) based on gelatin and crosslinked with gum Arabic have been prepared by the thaw–freezing method, employing two different concentrations of gum Arabic (15 and 50% w/w). Magnetic gels or ferrogels (FGs) were prepared by applying the breath in method to incorporate iron oxide magnetic nanoparticles to the HG matrix. The obtained HG and FG were characterized by XRD, FTIR, and SEM, and the FG composition was estimated by atomic absorption spectroscopy in terms of Fe content. The adsorption of crude oil onto HG and FG was explored achieving very satisfactory results. FG was regenerated by washing with toluene, maintaining efficiency of almost 90% after the fourth cycle. Equilibrium studies were performed to determine the capacity of the prepared FG for adsorption of crude oil from seawater synthetic solutions. The experiments were carried out as a function of different initial concentrations of oil residue (24 to 240 mg/L) exploring different contact times. Equilibrium data were found to fit very well with the Sips models. The kinetic data adsorption of oil onto the FG-15 was better fitted by a pseudo-second-order kinetic indicating that at the initial stages of adsorption, external mass transfer could control the whole rate of the crude oil uptake while intraparticle diffusion controlled the global rate of adsorption at later stages. The obtained results showed that the FG prepared by employing 15% of gum Arabic as the crosslinker (FG-15) has a high removal efficiency of crude oil reaching 1.53 g/g of FG at pH 5.5 and 0.59 g/g for oil/water emulsions in the order of 0.1 g/L. The magnetic properties extend its application. The reached data suggest that the materials presented here may be useful to further the design of systems or devices intended for the remediation of petroleum spills and/or its derivatives in marine water as well as other surfaces such as polluted rocks or soil.

Decomplexation of Cu(II)/Ni(II)-EDTA by ozone-oxidation process Abstract In this study, ozone-oxidation was used to treat synthetic chemical plating solution containing Cu(II)/Ni(II)-EDTA solution to realize the purpose of decomplexation. The effects of solution pH, initial concentration of Cu(II)/Ni(II)-EDTA, the molar ratio of EDTA to Cu(II)/Ni(II), and the coexistence of Cu(II)/Ni(II) on their removal efficiencies were investigated. The degradation of EDTA-Cu(II) and EDTA-Ni(II) were mainly attributed to OH oxidation, and the removal rates of Cu(II)/Ni(II) depend on the complete decomplexation. The removal rates of Cu(II) and Ni(II) was affected by the pH of solution, and the optimal pH was found to be 7–9; nevertheless, their removal rates can still be up to 90% even in acidic pHs of 3~5. When the molar ratio of EDTA to Cu(II)/Ni(II) increased from 1:1 to 3:1, the kinetics of metal ion removal rate declined from 0.0788 and 0.1139 min-1 to 0.0250 and 0.0271 min-1. The synergistic effect was found in the Cu(II)/Ni(II) blended system due to the higher catalytic capability and the lower complexation affinity toward EDTA for Ni(II). In summary, ozone oxidation can be considered as an effective technology to realize the complete decomplexation of Cu(II)/Ni(II)-EDTA that contained in chemical plating industry wastewater. Graphical Abstract

Characterization of Tagaran natural clay and its efficiency for removal of cadmium (II) from Sulaymaniyah industrial zone sewage Abstract The fine fraction of the Tagaran natural clay (TC) from the Kurdistan region of Iraq-Sulaimani was characterized and used to remove Cd ions from industrial swage. Using XRF, XRD, SEM, and FTIR, the dominant clay mineral of the Tagaran clay mineral was identified as saponite, with minor amounts of chlorite. The clay was examined for its efficiency to adsorb and remove (Cd2+) in the presence of other heavy metal contaminants from Sulaimani industrial zone sewage by a batch method. The effect of initial pH, equilibrium time, temperature, clay dosage, and Cd2+ concentration was studied. Results were evaluated using Langmuir, Freundlich, Temkin, and Redlich-Peterson isotherms. The kinetics could be best fitted to pseudo-second-order reaction kinetic model. In addition, the activation energy and the amount of calculated and experimentally determined heavy metal loads were consistent. The thermodynamic studies showed spontaneous endothermic adsorption. The trioctahedral smectite (saponite) showed a good efficiency for the adsorption of Cd2+ from the real sample (up to 100%) which at least partly can be explained by cation exchange. Tagaran clay is a candidate material for the production of an adsorber material for removing Cd2+ from aqueous solutions.

Remediation of BTEX and Cr(VI) contamination in soil using bioelectrochemical system—an eco-friendly approach Abstract Soil contamination with benzene, toluene, ethylbenzene and xylene isomers (BTEX) has raised increasing concern because of its high solubility in water and toxicity to biotic communities. This study aims at investigating the process and prospects of deploying bioelectrochemical system (BES) for the removal of BTEX from artificially contaminated soil using Pseudomonas putida YNS1, alongside the reduction of hexavalent chromium (Cr(VI)). The BES was setup with desired operating conditions: initial concentration of BTEX (50–400 mg/L in 100 mL of sterilized water), pH (4–10) and applied potential voltage (0.6–1.2 V) with 10 μL log-phase culture along with the addition of Cr(VI) (10 mg/L). Samples were collected at regular intervals and analysed for BTEX degradation using gas chromatography and Cr(VI) reduction using UV–Vis spectrophotometer. Under optimized conditions (initial BTEX concentration, 200 mg/L; pH 7; and applied voltage 0.8 V with Cr(VI) of 10 mg/L), 92% of BTEX was degraded and 90% Cr(VI) was reduced from the contaminated soil. The intermediates produced during degradation were analysed through gas chromatography-flame ionization detector (GC-FID), and the possible degradation pathway was elucidated. The results indicated that BES could be effective for simultaneous degradation of BTEX along with Cr(VI) reduction.