scholarly journals Zeolite for Potential Toxic Metal Uptake from Contaminated Soil: A Brief Review

Processes ◽  
2020 ◽  
Vol 8 (7) ◽  
pp. 820
Author(s):  
Claudia Belviso

Soil pollution is an increasingly urgent problem for the global environment. Soil can be contaminated with potential toxic metals from many anthropogenic activities, besides fossil fuel combustion and crude oil production, ranging from industry to mining and agriculture. Many technologies have been analysed to solve this type of environmental pollution and methods involving the use of minerals (e.g., clay minerals, zeolites, and natural silica adsorbents) are widely described in the literature. This article provides a summary of studies concerning the use of zeolites in soil remediation. A considerable number of these experiments were conducted using natural zeolites, while fewer concerned the utilization of synthetic zeolites. The mechanism controlling the successful application of these minerals was analysed through referring to global data published on this topic over the last few decades. This review also briefly discusses the limitations on zeolite applications and the drawbacks of the approaches analysed.

Science ◽  
1972 ◽  
Vol 175 (4027) ◽  
pp. 1279-1279
Author(s):  
K. K. Bertine ◽  
Edward D. Goldberg

2013 ◽  
Vol 13 (15) ◽  
pp. 7695-7710 ◽  
Author(s):  
Y. Takahashi ◽  
T. Furukawa ◽  
Y. Kanai ◽  
M. Uematsu ◽  
G. Zheng ◽  
...  

Abstract. Atmospheric iron (Fe) can be a significant source of nutrition for phytoplankton inhabiting remote oceans, which in turn has a large influence on the Earth's climate. The bioavailability of Fe in aerosols depends mainly on the fraction of soluble Fe (= [FeSol]/[FeTotal], where [FeSol] and [FeTotal] are the atmospheric concentrations of soluble and total Fe, respectively). However, the numerous factors affecting the soluble Fe fraction have not been fully understood. In this study, the Fe species, chemical composition, and soluble Fe concentrations in aerosols collected in Tsukuba, Japan were investigated over a year (nine samples from December 2002 to October 2003) to identify the factors affecting the amount of soluble Fe supplied into the ocean. The soluble Fe concentration in aerosols is correlated with those of sulfate and oxalate originated from anthropogenic sources, suggesting that soluble Fe is mainly derived from anthropogenic sources. Moreover, the soluble Fe concentration is also correlated with the enrichment factors of vanadium and nickel emitted by fossil fuel combustion. These results suggest that the degree of Fe dissolution is influenced by the magnitude of anthropogenic activity, such as fossil fuel combustion. X-ray absorption fine structure (XAFS) spectroscopy was performed in order to identify the Fe species in aerosols. Fitting of XAFS spectra coupled with micro X-ray fluorescence analysis (μ-XRF) showed the main Fe species in aerosols in Tsukuba to be illite, ferrihydrite, hornblende, and Fe(III) sulfate. Moreover, the soluble Fe fraction in each sample measured by leaching experiments is closely correlated with the Fe(III) sulfate fraction determined by the XAFS spectrum fitting, suggesting that Fe(III) sulfate is the main soluble Fe in the ocean. Another possible factor that can control the amount of soluble Fe supplied into the ocean is the total Fe(III) concentration in the atmosphere, which was high in spring due to the high mineral dust concentrations during spring in East Asia. However, this factor does not contribute to the amount of soluble Fe to a larger degree than the effect of Fe speciation, or more strictly speaking the presence of Fe(III) sulfate. Therefore, based on these results, the most significant factor influencing the amount of soluble Fe in the North Pacific region is the concentration of anthropogenic Fe species such as Fe(III) sulfate that can be emitted from megacities in Eastern Asia.


2006 ◽  
Vol 129 (4) ◽  
pp. 713-718 ◽  
Author(s):  
Hiroaki Hatanaka ◽  
Nobukazu Ido ◽  
Takuya Ito ◽  
Ryota Uemichi ◽  
Minoru Tagami ◽  
...  

Boiler piping of fossil-fuel combustion power generation plants are exposed to high-temperature and high-pressure environments, and failure of high-energy piping due to creep damage has been a concern. Therefore, a precise creep damage assessment method is needed. This paper proposes a nondestructive method for creep damage detection of piping in fossil-fuel combustion power generation plants by ultrasonic testing. Ultrasonic signals are transformed to signals in a frequency domain by Fourier transform, and a specific frequency band is chosen. To determine the creep damage, the spectrum intensities are calculated. Calculated intensities have a good correlation to life consumption of the weld joints, and this method is able to predict the remaining life of high-temperature piping, which has been already installed.


Agronomy ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 1354 ◽  
Author(s):  
Fanrong Zeng ◽  
Munazza Zahoor ◽  
Muhammad Waseem ◽  
Alia Anayat ◽  
Muhammad Rizwan ◽  
...  

Chromium (Cr) is recognized as a toxic metal that has detrimental effects on living organisms; notably, it is discharged into soil by various industries as a result of anthropogenic activities. Microbe-assisted phytoremediation is one of the most emergent and environmentally friendly methods used for the detoxification of pollutants. In this study, the alleviative role of Staphylococcus aureus strain K1 was evaluated in wheat (Triticum aestivum L.) under Cr stress. For this, various Cr concentrations (0, 25, 50 and 100 mg·kg−1) with and without peat-moss-based bacterial inoculum were applied in the soil. Results depicted that Cr stress reduced the plants’ growth by causing oxidative stress in the absence of S. aureus K1 inoculation. However, the application of S. aureus K1 regulated the plants’ growth and antioxidant enzymatic activities by reducing oxidative stress and Cr toxicity through conversion of Cr6+ to Cr3+. The Cr6+ uptake by wheat was significantly reduced in the S. aureus K1 inoculated plants. It can be concluded that the application of S. aureus K1 could be an effective approach to alleviate the Cr toxicity in wheat and probably in other cereals grown under Cr stress.


2020 ◽  
Author(s):  
Haiyan Ni ◽  
Ru-Jin Huang ◽  
Ulrike Dusek

<p>To investigate the sources and formation mechanisms of carbonaceous aerosols, a major contributor to severe particulate air pollution, radiocarbon (<span><sup>14</sup>C</span>) measurements were conducted on aerosols sampled from November 2015 to November 2016 in Xi'an, China. Based on the <span><sup>14</sup>C</span> content in elemental carbon (EC), organic carbon (OC) and water-insoluble OC (WIOC), contributions of major sources to carbonaceous aerosols are estimated over a whole seasonal cycle: primary and secondary fossil sources, primary biomass burning, and other non-fossil carbon formed mainly from secondary processes. Primary fossil sources of EC were further sub-divided into coal and liquid fossil fuel combustion by complementing <span><sup>14</sup>C</span> data with stable carbon isotopic signatures.</p><p>The dominant EC source was liquid fossil fuel combustion (i.e., vehicle emissions), accounting for 64 % (median; 45 %–74 %, interquartile range) of EC in autumn, 60 % (41 %–72 %) in summer, 53 % (33 %–69 %) in spring and 46 % (29 %–59 %) in winter. An increased contribution from biomass burning to EC was observed in winter (<span>∼28</span> %) compared to other seasons (warm period; <span>∼15</span> %). In winter, coal combustion (<span>∼25</span> %) and biomass burning equally contributed to EC, whereas in the warm period, coal combustion accounted for a larger fraction of EC than biomass burning. The relative contribution of fossil sources to OC was consistently lower than that to EC, with an annual average of <span>47±4</span> %. Non-fossil OC of secondary origin was an important contributor to total OC (<span>35±4</span> %) and accounted for more than half of non-fossil OC (<span>67±6</span> %) throughout the year. Secondary fossil OC (SOC<span><sub>fossil</sub></span>) concentrations were higher than primary fossil OC (POC<span><sub>fossil</sub></span>) concentrations in winter but lower than POC<span><sub>fossil</sub></span> in the warm period.</p><p>Fossil WIOC and water-soluble OC (WSOC) have been widely used as proxies for POC<span><sub>fossil</sub></span> and SOC<span><sub>fossil</sub></span>, respectively. This assumption was evaluated by (1) comparing their mass concentrations with POC<span><sub>fossil</sub></span> and SOC<span><sub>fossil</sub></span> and (2) comparing ratios of fossil WIOC to fossil EC to typical primary OC-to-EC ratios from fossil sources including both coal combustion and vehicle emissions. The results suggest that fossil WIOC and fossil WSOC are probably a better approximation for primary and secondary fossil OC, respectively, than POC<span><sub>fossil</sub></span> and SOC<span><sub>fossil</sub></span> estimated using the EC tracer method.</p>


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