A plethora of empirical work explored finance-income-environment nexus, aims to investigate high CO₂ emissions determinants, over the last few couples of decades. The prior empirical work assist the idea that finance and income have diverse impacts on the environment. The lack of consensus on finance-income-environment nexus in the Central and Eastern European Countries in the perspective of Belt and Road Initiative need to be examined. Therefore, the present study explores the nexus between financial development, income level, and environmental quality for a panel of eighteen Central and Eastern European Countries, over the period of 1980–2016. The Dynamic Seemingly Unrelated Regression, the Fully Modified Ordinary Least Squares, and the Dumitrescu-Hurlin panel casualty approaches are employed. The environmental Kuznets curve hypothesis also investigated for both time series panel and country-wise. The Dynamic Seemingly Unrelated Regression long-run panel results reveal that (i) financial development index and income negatively impact on environmental quality; (ii) energy consumption is the key determinant of CO₂ emissions and reduces environmental quality; (iii) urbanization and trade both enhance environmental quality via reduction of carbon emissions; and (iv) the environmental Kuznets curve hypothesis supported for the selected panel countries. The country-wise results depict that increase in environmental quality occurs due to increase in financial development (in four countries), income level (in five countries), trade (in five countries), and urbanization (in eight countries). However, the environmental quality decreases due to the increase in financial development (in six countries), income level (in eight countries), energy consumption (in twelve countries), trade (in six countries), and urbanization (in five countries). The environmental Kuznets curve hypothesis supported for five Central and Eastern European Countries. Additionally, the causality results confirmed the presence of feedback relationships among income and environmental quality, and financial development and energy consumption. Thus, we conclude that income level and financial development are the main drivers behind high carbon dioxide emissions in CEECs. The finding of the study opens up new insight for appropriate policymaking.

Metropolitan areas may suffer with increase of air pollution due to the growth of urbanization, transportation, and industrial sectors. The Metropolitan Area of Vitória (MAV) in Brazil is facing air pollution problems, especially because of the urbanization of past years and of having many industries inside the metropolitan area. Developing air quality system is crucial to understand the air pollution mechanism over these areas. However, having a good input dataset for applying on photochemical models is hard and requires quite of research. One input file for air quality modeling which can play a key role on results is the lateral boundary conditions (LBC). This study aimed to investigate the influence of LBC over CMAQ simulation for particulate matter and ozone over MAV by applying four different methods as LBC during August 2010. The first scenario (M1) is based on a fixed, time-independent boundary conditions with zero concentrations for all pollutants; the second scenario (M2) used a fixed, time-independent concentration values, with average values from local monitoring stations; the third CMAQ nesting scenario (M3) used the nested boundary conditions varying with time from a previous simulation with CMAQ over a larger modeling domain, centered on MAV; and finally, the fourth GEOS-Chem scenario (M4) used the boundary conditions varying with time from simulations of global model GEOS-Chem. All scenarios runs are based on the same meteorology conditions and pollutant emissions. The air quality simulations were made over a domain 61 × 79 km centered on coordinates − 20.25° S, − 40.28° W with a resolution of 1 km. The results were evaluated with the measured data from the local monitoring stations. Overall, significant differences on concentrations and number of chemical species between the LBC scenarios are shown across all LBC scenarios. The M3 and M4 dynamic LBC scenarios showed the best performances over ozone estimates while M1 and M2 had poor performance. Although no LBC scenarios do not seem to have a great influence on total PM₁₀ and PM₂.₅ concentrations, individual PM₂.₅ species like Na, NO₃⁻, and NH₄⁺concentrations are influenced by the dynamic LBC approach, since those hourly individual PM₂.₅ species from CMAQ nesting approach (M3) and GEOS-Chem model (M4) were used as an input to LBC.

To reduce the environmental pollution caused by ammonium paratungstate (APT) production in the Ganzhou area in China, simulated experiments in laboratory and field experiments in cement kilns were performed. The migration characteristics of As in secondary residues (thermometallurgy and hydrometallurgy residues) from APT production in cement kilns were similar, and As in the residues existed in the form of sulfides. When the residues were fed at the kiln inlet, the As in the residues was completely distributed in the clinker after a new mass balance of As was reestablished in a very short time. When the residues were fed at the raw mill, the total input rate of As was far higher than the total output rate. Therefore, a part of As was circulated in the cement kiln, and only a small part of As was distributed in the clinker. In addition, the As concentration in the flue gas and the leaching concentration of As in the clinker were far below the limit value in the Chinese standard. For feeding rates below that are used in the field experiment, co-processing of secondary residues in a cement kiln fed at the kiln inlet is environmentally safe. However, if the secondary residues are consistently fed at the raw mill, the As concentration in the flue gas may gradually increase.

The presence of toxic metals in soil enables them to be absorbed by plants. The RDC 42/2013 published by Brazilian Health Regulatory Agency (ANVISA) defines the maximum values of cadmium (0.4 mg kg⁻¹) and lead (0.6 mg kg⁻¹) in yerba mate commercialized in Common Market of the South (Mercosul). This work is a retrospective study that aimed to evaluate cadmium and lead levels in processed yerba mate and in natura leaves in Southern Brazil. The cadmium and lead concentrations in 370 processed yerba mate and 122 in natura leave samples obtained in Southern Brazil were analyzed. In 47.56% of the processed samples, the levels of cadmium and/or lead were found to be above the authorized levels. The cadmium levels found in the processed yerba mate were 0.37 ± 0.19 mg kg⁻¹, and the corresponding values for lead were 0.34 ± 0.21 mg kg⁻¹. Values above the authorized levels were also found in the non-processed leaves. Studies are required to determine whether these levels are natural or represent contamination.

The objective of this study is to identify the feasibility of using rhamnolipid biosurfactant to remediate heavy metals contained in manganese nodules collected from the Clarion-Clipperton Fracture Zone, Pacific Ocean. Deep-sea manganese nodules may represent one of the most important future natural resources for heavy metals due to the depletion of resources on land. Since international marine environment guidelines for deep-sea mining will be set up by international organisations in the 2020s, remediation technologies are urgently required for deep-sea mining tailings. We show that rhamnolipid biosurfactant is an environmentally friendly substance and can be successfully used for the remediation of heavy metals in deep-sea mining tailings under various reaction conditions. Rhamnolipids therefore represent a useful extracting agent for heavy metals in deep-sea mining tailings. The removal of nickel (Ni), copper (Cu), and cadmium (Cd) would be enhanced in the presence of rhamnolipids with specific reaction times and concentrations. Future actual remediation technologies should be developed using rhamnolipid biosurfactant on the basis of these results.

Ammonia is one of the most common aquatic pollutants. To analyze the effect of ammonia exposure on the glutathione redox system, we investigated the levels of hydrogen peroxide (H₂O₂) and glutathione, and transcription and activities of glutathione-related enzymes in liver and gills of FFRC strain common carp (Cyprinus carpio L.) exposed to 0, 10, 20, and 30 mg/L of ammonia. The results showed that H₂O₂ content reached a maximum level at 48 h of exposure in the liver of fish. In gills, H₂O₂ increased rapidly at 6 h and reached to maximum levels at 24 h of exposure, indicating that gills experienced oxidative stress earlier than the liver of fish exposed to ammonia. Reduced glutathione (GSH) content and reduced glutathione/oxidized glutathione (GSH/GSSG) ratio increased significantly within 24 h of exposure. Meanwhile, the transcription and activities of glutathione S-transferase (GST) and glutathione reductase (GR) increased significantly in the liver, and glutathione peroxidase (GSH-Px) and GST increased in the gills of fish exposed to ammonia. Malondialdehyde (MDA) content kept at a low level after exposure to low concentration of ammonia, but increased significantly after exposure to 30 mg/L ammonia for 48 h along with a decrease in GSH content and GSH/GSSG ratio. These data showed that the glutathione redox system played an important role in protection against ammonia-induced oxidative stress in the liver and gills of FFRC strain common carp, though the defense capacity was not able to completely prevent oxidative damage occurring after exposure to higher concentration of ammonia. This research systematically studied the response of the glutathione redox system to ammonia stress and would provide novel information for a better understanding of the adaptive mechanisms of fish to environmental stress.

Since decades, surface water bodies have been exposed to pesticides from agriculture. In many places, retention systems are regarded as an important mitigation strategy to lower pesticide pollution. Hence, the processes governing the transport of pesticides in and through a retention system have to be understood to achieve sufficient pesticide attenuation. In this study, the temporal dynamics of metazachlor and its transformation products metazachlor-oxalic acid (OA) and –sulphonic acid (ESA) were observed in an agricultural retention pond and hydrologic tracers helped to understand system-inherent processes. Pesticide measurements were carried out for 80 days after their application during transient flow conditions. During a short-term (3 days) experiment, the tracers bromide, uranine and sulphorhodamine B were used to determine hydraulic conditions, residence times and sorption potential. A long-term experiment with sodium naphthionate (2 months) and isotopes (12 months) provided information about inputs via interflow and surface-groundwater interactions. During transient conditions, high concentration pulses of up to 35 μg L⁻¹ metazachlor, 14.7 μg L⁻¹ OA and 22.5 μg L⁻¹ ESA were quantified that enduringly raised solute concentrations in the pond. Mean residence time in the system accounted for approximately 4 h showing first tracer breakthrough after 5 min and last tracer concentrations 72 h after injection. While input via interflow was confirmed, no evidence for surface-groundwater interaction was found. Different tracers illustrated potentials for sorption and photolytic degradation inside the system. This study shows that high-resolution sampling is essential to obtain robust results about retention efficiency and that hydrological tracers may be used to determine the governing processes.

Nitrogen removal by anammox process has been recognized as efficient, cost-effective, and low-energy alternative removal. The longer start-up periods of anammox process hindered the widespread application of anammox-based technology. In this study, four identical unplanted subsurface-flow constructed wetlands (USFCWs) were built up to investigate the effects of electron acceptors (Fe³⁺, Mn⁴⁺, SO₄²⁻) on the start-up of anammox process. Results indicated that the start-up time of anammox process was shortened to 105 days in R1 (with Fe³⁺ addition) and 110 days in R2 (with Mn⁴⁺ addition) with nitrogen removal efficiencies of above 75%, compared with 148 days in R0 (control). The addition of SO₄²⁻ had no significant effect on start-up process. High-throughput sequencing results demonstrated that Shannon index increased significantly from 2.87 (R0) to 5.08 (R1) and 5.00 (R2), and the relative abundance of Candidatus Anammoxoglobus rose from 3.6 to 5.3% in R1. Denitratisoma increased significantly in R2 under addition of Mn⁴⁺, which was beneficial for the occurrence of anammox process. The functional genes that related to signal transduction mechanisms and secondary metabolite biosynthesis, transport, and catabolism were upregulated after addition of electron acceptors. These results demonstrated that adding electron acceptors Fe³⁺ or Mn⁴⁺ could be an effective way to accelerate the start-up of anammox process. Graphical abstract ᅟ

Sorption of oil-related products (including mainly the propellants) is the very basic process that counteracts spreading these types of pollution into environment. Plenty of synthetic substances (including the monoaromatic hydrocarbons) are both from the surface and underground waters. The aim of this study was to present the research’s results on the possibilities of using the broadleaf cattail (Typha latifolia L.) seeds as a sorbent of monoaromatic hydrocarbons from an aqueous solution. In order to increase sorptive capacity, the seeds biomass was submitted for the process of mercerizing in diversified time and temperature in water and the NaOH solution. The removal of benzene, toluene, ethylbenzene, o-xylene, m-xylene and cumene was carried out by means of the “batch method”. All the conducted experiments have shown a high sorption level of the analysed pollutions from an aqueous solution. The best sorptive qualities appeared in the seeds drenched in 80 °C water for 4 h (W) 97 g/kg, what was 9.06% more absorbed hydrocarbons in comparison to the control sample (C) and 26.8% more than the smallest seeds drenched in NaOH for 240 min. in the temperature of 80 °C (N). The process of the seeds mercerizing that was conducted with the use of hot water appeared to be most effective, but seeds without mercerisation (C) is actually the material which absorbs the least amounts of energy for preparation and had quite good sorption capacity too.

This research work is focused on the synthesis, characterization, and application of cost-effective biochar–biopolymeric hybrid adsorbents from waste agricultural biomass and sodium alginate. The adsorbents were characterized by BET (Brunauer–Emmett–Teller), FTIR (Fourier transform infrared), XRD (X-ray diffraction), FESEM (field emission scanning electron microscopy), and bulk density measurement. The performance of the synthesized hybrid adsorbents has been tested for the removal of aqueous phase Ni²⁺ and Cu²⁺ metal ions at a concentration range of 25 to 100 mg/L, adsorbent dose of 1–3 g/L, and system temperature of 298–308 K, respectively. The effect of various physicochemical process parameters such as solution pH, adsorbent dose, initial metal ion concentration, temperature, and presence of salts on metal ion adsorption has been studied here, and experimental process parameters are being optimized by response surface methodology (RSM). The model was fitted well with the experimental data. Various kinetic models, namely, pseudo-first-order, pseudo-second-order, and Weber–Morris, have been fitted with batch experimental data, and the mechanism of adsorption has been identified. The maximum Langmuir monolayer adsorption capacity for Cu²⁺ and Ni²⁺ were 112 and 156 mg/g, respectively, which are comparative to other published adsorbent’s capacity data under similar experimental conditions. Thermodynamic parameter studies showed that the system was endothermic and spontaneous in nature.