Heavy metals including copper (Cu), zinc (Zn), cadmium (Cd), chromium (Cr), lead (Pb), and arsenic (As) were investigated in 89 pairs of rice plant and paddy soils around Dongting Lake area, China. Rice plants and soils were collected with GPS device, and heavy metal contents in different rice plant tissues and soils were measured. The aim of the present study was to assess the heavy metal pollution and translocation in the whole soil-rice system, including the consequent human health risk for residents. According to the indices of average geoaccumulation (Igₑₒ) of the studied elements, paddy soils in study area were moderately polluted by Cd, lowly polluted by Pb, and not polluted by Cu, Zn, Cr, and As. Considering the much higher concentrations of studied elements in roots than in other tissues of rice plants, a great mass of these elements was assumed to be confined in the roots. The low translocation factors from root to shoot (Tfᵣₒₒₜ₋ₛₕₒₒₜ) of all the studied heavy metals (0.04–0.74) underpinned this. The high translocation factors from soil to root (Tfₛₒᵢₗ₋ᵣₒₒₜ) of Cd (9.12), As (4.38), and Zn (2.05) indicated the high bioavailability of these heavy metals for rice plant. The health risk assessment using target hazard quotients (THQs) model indicated that Cd (5.17 for adults and 4.49 for children respectively) and As (3.61 for adults and 3.14 for children respectively) could cause human health risk both for adults and children. Further, given the rate of individual THQ values exceeding one, Cu might also be considered as a potential human health dangerous element in the study area. It was worth noting that as one of the main pollutants, Pb did not show human health risk through rice grain consumption due to its low Tf values in soil-rice system. However, the risk identification of As using comparisons of measured concentrations with risk screening value in Chinese paddy soil standard (GB15618-2018) was not consistent with the human health risk assessment result. This might indicate that site-specific risk screening values of As in China is in demand.

Brownfields have attracted increasing attentions from both researchers and practitioners. However, few studies have attempted to make a comprehensive and quantitative review on this topic. This study conducted a scientometric review on the brownfield research from 1995 to 2017 using CiteSpace. The knowledge structure, hot topics, research trends, and gaps were analyzed based on the co-author, co-word, co-citation, and clusters analysis. Six hundred thirty articles from the Web of Science core collection database were selected as the research samples. Results revealed that the research focus has changed from soil remediation technologies to sustainable regeneration methods. The most vital development in brownfield research occurred in the USA, England, Canada, Germany, and China. “Brownfield,” “heavy metal,” “remediation,” “redevelopment,” and “sustainability” were the most frequently used keywords. Whereas “management” and “biodiversity” received citation bursts in recent years. Existing researches mainly concentrated on subject categories of environmental sciences ecology, environmental sciences, engineering, environmental studies, engineering environmental, and urban studies. Sustainable regeneration, urban brownfields’ regeneration, mental distribution, coal-mine brownfield, and ecosystem service were the identified co-citation clusters and represented the hot topics and emerging trends. The research gaps can serve as a motivation to research on the next generation of brownfields to support the sustainable development. This study provides researchers and practitioners an extensive and intensive understanding of the salient research themes and trends of brownfields’ research worldwide.

In the present work, graphene oxide (GO) was synthesized via the modified Hummers method and utilized in treating real soil washing wastewater via adsorptive removal of lead (Pb) and zinc (Zn). Characterization analysis of GO was performed using X-ray diffraction, Brunauer-Emmett-Teller method, Fourier transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, and zeta potential analysis. The Van’t Hoff, Eyring, and Arrhenius equations were applied to determine the activation and thermodynamic parameters namely activation energy (Eₐ), standard Gibbs energy change (ΔG°), standard enthalpy change (ΔH°), standard entropy change (ΔS°), change in activation Gibbs energy (ΔG#), change in activation enthalpy (ΔH#), and change in activation entropy (ΔS#). Based on the high coefficient of determination values (0.8882 ≥ R² ≥ 0.9094) and low values of SSE (0.0292 ≤ SSE ≤ 0.0511) and ARE (0.8014 ≤ ARE ≤ 0.8822), equilibrium data agreed well with the Freundlich isotherm. The maximum adsorption capacity for Pb(II) and Zn(II) was determined to be 11.57 and 4.65 mg/g, respectively. Kinetic studies revealed that pseudo-second-order equation fitted well with the experimental data, which indicates that chemisorption is the rate-determining step of the adsorption system. Results have shown the possibility of GO as a potential adsorbent material in the treatment of soil washing wastewater.

The paper reviews the existing applications of sensing technologies for measuring construction off-road vehicle emissions (COVE) such as earthmoving equipment. The current literature presented different measurement methods and reported the results of utilisation of new technologies for measuring COVE. However, previous papers used different technology applications covering only a part of the monitoring process with its own limitations. Since technologies are advancing and offering novel solutions, there is an urgent need to identify the gaps, re-evaluate the current methods, and develop a critical agenda for automating the entire process of collecting emissions data from construction sites, and monitoring the emission contributors across cities. This paper systematically identifies relevant papers through a search of three key databases—Web of Science, Engineering Valley and Scopus—covering the publications in the last decade from 2008 to 2017. An innovative robust research method was designed to select and analyse the relevant papers. The identified papers were stored in a data set, and a thematic algorithm employed to find the clusters of papers which might be potentially relevant. The selected papers were used for further micro-thematic analysis to find key relevant papers on COVE, and the gap in the literature. A sample of relevant papers was found relevant to COVE and critically reviewed by coding and content analysis. This paper critically reviews the selected papers and also shows that there is a considerable gap in the applications of new technologies for measuring in-use COVE in real time based on real activities toward automated methods. This review enables practitioners and scholars to gain a concrete understanding of the gap in measuring COVE and to provide a significant agenda for future technology applications.

Arsenic (As) is considered as one of the most hazardous elements found in the groundwater. It is present in water in both arsenate (As(V)) and arsenite (As(III)) forms. On exposure for a considerable length of time to water having As concentration above the maximum permissible limit of 10 μg/L, there is a serious threat of developing various health problems including cancer. There is frequent reporting about the development of different newer methods for the removal of arsenic from water. In this present approach, a low-cost product namely modified paddy husk ash (PHA) was used as an adsorbent for the adsorption of arsenic from water. The adsorbent is important from the point of its easy availability in the tropical paddy producing countries. For improved removal efficiency and disposal of spent adsorbent, the surface of the PHA was activated with an aluminum oligomeric solution called as hydroxyl-alumina. To understand the process, various techniques such as XRD, SEM–EDS, particle size determination, and zeta potential measurements were used and the effects like variation of adsorbent dose, pH, initial arsenic concentration, and contact time were studied. The Freundlich adsorption isotherm and pseudo-second-order kinetic models were found to be the best fitted adsorption isotherm and kinetic data models respectively thereby confirming the adsorption as a multilayer chemisorption process. Finally, the issue of disposal of the spent sludge through the successful formation of cement clinkers was studied.

Coal mine dust continues to be a health and safety issue in underground coal mines. Coal seam water infusion was developed and widely applied in European coal mines for dust control, and was also a common practice in most Chinese coal mines. This method typically involves the infusion of water into the coal seam to increase its moisture content, and therefore reduce dust generation during mining operations. With the availability of other dust control methods such as water spraying systems, the water infusion method has not been considered as a viable means for dust mitigation in modern mines. However, the increase in production output and the deployment of more powerful equipment for coal cutting and transport and intensive gas drainage practices mean that workers could be exposed to more dust contaminations. Whilst the mine operators are committed to suppress and dilute airborne dust particles using these passive measures, there is a need to critically examine and subsequently develop this proactive dust control technology for practical applications in Chinese coal mines. The paper provides a critical review of the water infusion technologies in view of its technological advances and practical application limitations. The methods of water infusion, mechanism of water flow in coal, the role of surfactants and the key parameters influencing the effect of water infusion on dust control are identified and discussed. Existing problems and prospects for water infusion are analysed.

In this paper, nanosized titanium dioxide as catalysts for degrading dye wastewater was in situ synthesized on the surface of cotton fabrics used tetrabutyl titanate as precursor. The morphology and structure of prepared catalysts were characterized by scanning electron microscopy, energy-dispersive spectrometer, and X-ray diffraction. The characterization results showed that anatase nanosized titanium dioxide was successfully synthesized in situ on cotton fabrics and had excellent dispersibility. Subsequently, the effects of irradiation time, catalyst dosage, dye concentration, initial pH value of dye, hydrogen peroxide dosage, and dye type on dye degradation rate were investigated one by one by a photocatalytic performance test. The test results indicated that the degradation rates of methylene blue, methyl orange, and rhodamine B were 90.4%, 81.4%, and 58.3%, separately, at catalyst dosage of 4.8 g/L, initial dye concentration of 10 mg/L, pH of 7, and hydrogen peroxide dosage of 0.24 mol/L, after 4 h of UV irradiation.

The effects of elevated ozone (O₃) levels (80 ppb and 120 ppb) on photosynthetic efficiency and growth of canola plants were studied in open-top chambers. The chlorophyll a polyphasic fluorescence rise kinetics OJIP, stomatal conductance and Chlorophyll Content Index (CCI) were measured after 15 and 30 days of O₃ fumigation, as well as in control plants; biomass measurements were done only after 30 days with and without fumigation. Analysis of the OJIP kinetics by the JIP-test led to the calculation of several photosynthetic parameters and the total Performance Index (PIₜₒₜₐₗ). The decline of PIₜₒₜₐₗ under the 80 ppb O₃ treatment was due to a lower density of reaction centres (RC/ABS), while the notable decline under the 120 ppb treatment was found to be due both to a further decline of RC/ABS and to a pronounced lowering of the efficiency with which an electron can move from the reduced intersystem electron acceptors to the PSI end acceptors (δRₒ). Stomatal conductance was affected by both treatments. Biomass was found to be affected by O₃ fumigation (for 30 days), decreasing by 40% at 80 ppb and by more than 70% under 120 ppb. Our findings indicate that biomass decline is due both to the lowering of CCI and the lowering of photosynthetic efficiency parameters. They thus suggest that two simple, non-invasive and rapid methods, namely, the analysis of OJIP fluorescence transients and the measurement of CCI, can be used to screen the effect of elevated O₃ on biomass of canola plants.

Macroporous resin-supported reagents have been identified as potential adsorbents for removal of toxic pollutants. This article presents an experimental designed to evaluate the sorption and desorption of nickel(II) with the help of column and batch procedure using simple extractant-impregnated resin (EIR). Isonitroso-4-methyl-2-pentanone (IMP) as an extractant was impregnated on a solid support like Amberlite XAD-4 to prepare the EIR sorbent. Column experimental conditions such as pH, sample flow rate and volume, eluting solution, and interfering ions were studied to optimize the nickel(II) sorption and recovery from aqueous media. The column results suggest that the quantitative nickel(II) sorption was observed at pH 5–6, and the quantitative recovery (≥ 95%) was achieved by using 1.0 M HNO₃. The high concentrations of cations and anions (except EDTA) present in the spiked binary and multi-element mixture solution show no interferences in both quantitative sorption and recovery of nickel(II), whereas the batch experiments were performed to evaluate nickel(II) sorption behavior using the linearized and non-linearized kinetic and isotherm models. By error function analysis, the Freundlich isotherm and the pseudo-first-order kinetic model were found to describe best the experimental data obtained over the studied concentration range and sorption time, respectively. The maximum sorption capacity of nickel(II) onto the EIR sorbent was found to be ~ 81 mg/g. The mean free energy (E = 10.1 kJ/mol) determined using Dubinin-Radushkevich isotherm suggests chemical nature of nickel(II) sorption on EIR. The novelty of the EIR adsorbent lies in its potential for separation and recovery of nickel(II) at trace level in water samples of different origin.

Cadmium contamination of agricultural soils has aroused worldwide concern because of the threats posed to human health through accumulation in food chains. A greenhouse pot experiment was conducted with in situ Cd-contaminated soil to study the influence of different potassium fertilizers (KCl, K₂SO₄, and KNO₃) on Cd accumulation in rice, wheat, and pak choi as well as the NH₄NO₃-extractable Cd (NEX-Cd) content in soils. In our study, rice and wheat biomass increased in the presence of K fertilizers, whereas pak choi biomass remained stable. Moreover, our experiment demonstrated that Cl⁻ increased Cd uptake by crops more effectively than SO₄²⁻ or NO₃⁻. The KCl treatments increased the Cd content of all three crops; as the KCl dose was increased, the Cd content of rice grains, wheat grains, and pak choi shoots increased by 10.8–192.8%, 17.1–67.7%, and 15.1–40.4%, respectively. The KNO₃ treatment also increased the Cd content of all three crops; however, the K₂SO₄ treatment only slightly increased the Cd content of wheat and pak choi and greatly decreased the Cd content of rice. In addition, both of the NEX-Cd content of wheat soil and pak choi soil were much higher than that of rice paddy soil. The KCl treatment resulted in a significant increase in the NEX-Cd content of rice paddy soil, but there were no significant differences in the NEX-Cd content of wheat soil or pak choi soil, regardless of which types or doses of K fertilizers were supplied. Based on these results, when K fertilizers are applied to Cd-contaminated soils, both types and doses should be carefully considered to mitigate Cd accumulation in crops, especially the edible part.