Airborne PCDD/Fs in two e-waste recycling regions after stricter environmental regulations

Since the 2010 s, the authorities of Guangdong province and local governments have enhanced law enforcement and environmental regulations to abolish open burning, acid washing, and other uncontrolled e-waste recycling activities. In this study, ambient air and indoor dust near different kinds of e-waste recycling processes were collected in Guiyu and Qingyuan to investigate the pollution status of particles and polychlorinated dibenzo-pdioxins and furans(PCDD/Fs) after stricter environmental regulations. PM_(2.5) and PCDD/Fs both showed significantly reduced levels in the two regions compared with the documented data. The congener distribution and principal component analysis results also confirmed the significant differences between the current PCDD/Fs pollution characterizations and the historical ones. The estimated total intake doses via air inhalation and dust ingestion of children in the recycling region of Guiyu ranged from 10 to 32 pg TEQ/(kg·day), which far exceeded the tolerable daily intake(TDI) limit(1–4 pg TEQ/(kg·day). Although the measurements showed a significant reduction of the release of PCDD/Fs, the pollution status was still considered severe in Guiyu town after stricter regulations were implemented.     

加油站油气回收现状与展望

通过理论计算和案例分析,对目前在用加油站油气回收系统的有效运行率进行了分析,阐述加油站三次油气回收装置的配备条件,介绍了加油站油气回收新技术(ORVR),提出了我国应使用新的加油站油气回收技术的结论。     

PICRUSt2 functionally predicts organic compounds degradation and sulfate reduction pathways in an acidogenic bioreactor

• Over 70% reduction of sulfate was achieved for sulfate less than 12000 mg/L. • The decrease of genes encoding (EC: 1.3.8.1) induced the accumulation of VFAs. • The sulfate reduction genes were primary carried by genus Desulfovibrio. • Sulfate favored assimilatory, but inhibited dissimilatory sulfate reduction process. For comprehensive insights into the influences of sulfate on performance, microbial community and metabolic pathways in the acidification phase of a two-phase anaerobic system, a laboratory-scale acidogenic bioreactor was continuously operated to treat wastewater with elevated sulfate concentrations from 2000 to 14000 mg/L. The results showed that the acidogenic bioreactor could achieve sulfate reduction efficiency of greater than 70% for influent sulfate content less than 12000 mg/L. Increased sulfate induced the accumulation of volatile fatty acids (VFAs), especially propionate and butyrate, which was the primary negative effects to system performance under the high-sulfate environment. High-throughput sequencing coupled with PICRUSt2 uncovered that the accumulation of VFAs was triggered by the decreasing of genes encoding short-chain acyl-CoA dehydrogenase (EC: 1.3.8.1), regulating the transformation of propanoyl-CoA to propenoyl-CoA and butanoyl-CoA to crotonyl-CoA of propionate and butyrate oxidation pathways, which made these two process hardly proceed. Besides, genes encoding (EC: 1.3.8.1) were mainly carried by order Clostridiales. Desulfovibrio was the most abundant sulfate-reducing bacteria and identified as the primary host of dissimilatory sulfate reduction functional genes. Functional analysis indicated the dissimilatory sulfate reduction process predominated under a low sulfate environment, but was not favored under the circumstance of high-sulfate. With the increase of sulfate, the assimilatory sulfate reduction process finally overwhelmed dissimilatory as the dominant sulfate reduction pathway in acidogenic bioreactor.     

Nutrient leaching in extensive green roof substrate layers with different configurations

Environmental Science and Pollution Research - Due to substrate layers with different substrate configurations, extensive green roofs (EGRs) exhibit different rainfall runoff retention and...     

The combined toxicity and mechanism of multi-walled carbon nanotubes and nano copper oxide toward freshwater algae: Tetradesmus obliquus

Nanoparticles(NPs) are widely used for their special physical properties and released into the natural environment. When two types of NPs exist in the same environment, the presence of one type of NP may affect the properties of the other type of NP. This study investigated the toxic effects of multi-walled carbon nanotubes(MWCNTs) and copper oxide nanoparticles(Cu O NPs) on Tetradesmus obliquus. Both NPs had toxic effects on algae, and the toxic effects of MWCNTs were significantly stronger tha...     

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.     

Mercury transformation processes in nature: Critical knowledge gaps and perspectives for moving forward

The transformation of mercury (Hg) in the environment plays a vital role in the cycling of Hg and its risk to the ecosystem and human health. Of particular importance are Hg oxidation/reduction and methylation/demethylation processes driven or mediated by the dynamics of light, microorganisms, and organic carbon, among others. Advances in understanding those Hg transformation processes determine our capacity of projecting and mitigating Hg risk. Here, we provide a critical analysis of major knowledge gaps in our understanding of Hg transformation in nature, with perspectives on approaches moving forward. Our analysis focuses on Hg transformation processes in the environment, as well as emerging methodology in exploring these processes. Future avenues for improving the understanding of Hg transformation processes to protect ecosystem and human health are also explored.     

Biochar affects methylmercury production and bioaccumulation in paddy soils: Insights from soil-derived dissolved organic matter

Biochar has been used increasingly as a soil additive to control mercury (Hg) pollution in paddy rice fields. As the most active component of soil organic matter, soil dissolved organic matter (DOM) plays a vital role in the environmental fate of contaminants. However, there are very few studies to determine the impact of biochar on the Hg cycle in rice paddies using insights from DOM. This study used original and modified biochar to investigate their effect on DOM dynamics and their potential impact on methylmercury (MeHg) production and bioaccumulation in rice plants. Porewater DOM was collected to analyze the variations in soil-derived DOM in paddy soils. The results showed that the addition of biochar, whether in original or modified form, significantly reduced the bioaccumulation of MeHg in rice plants, especially in hulls and grains (p<0.05). However, MeHg production in soils was only inhibited by the modified biochar. Biochar addition induced a significant increase in DOM's aromaticity and molecular weight (p<0.05), which decreased Hg bioavailability. Furthermore, enhanced microbial activity was also observed in DOM (p<0.05), further increasing MeHg production in the soil. Thus, the effect of biochar on the fate of Hg cycle involves competition between the two different roles of DOM. This study identified a specific mechanism by which biochar affects Hg behavior in rice paddy soil and contributes to understanding the more general influence of biochar in agriculture and contaminant remediation.     

Understanding the excretion rates of methylmercury and inorganic mercury from human body via hair and fingernails

Effective biomarkers are necessary to better understand the human mercury (Hg) exposure levels. However, mismatched biomarker sampling method causes extra uncertainty in assessing the risk of Hg exposure. To compare the differences between hair and fingernail, and further understand the excretion rates of methylmercury (MeHg) and inorganic mercury (IHg) via hair and fingernails, the total mercury (THg), MeHg, and IHg concentrations in paired hair and fingernail samples were investigated through paired samples collected from two typical mining areas, Wanshan mercury mine area (WMMA) and Hezhang zinc smelting area (HZSA). The positive correlation in THg, MeHg, and IHg concentrations (p <0.01) between hair and fingernail samples indicated that those two biomarkers can be corrected in application of assessing human Hg exposure. Compared to fingernails, the hair was suggested to be a more sensitive biomarker as the concentration of THg, MeHg and IHg were 2 ∼ 4 times higher than those in fingernails. Furthermore, the amounts of THg, MeHg, and IHg excreted via hair were 70 ∼ 226 times higher than that excreted via fingernails, and the hair plays a more important role than fingernails in the excretion of Hg from human bodies. Present study therefore provides some new insights to better understand the fate of human assimilated Hg.     

Highly efficient Hg2+ removal via a competitive strategy using a Co-based metal organic framework ZIF-67

The stronger coordination ability of mercury ions with organic ligands than the metal ions in metal organic framework (MOFs) provides an accessible way to separate mercury ions from solution using specific MOFs. In this study, a Co-based MOF (ZIF-67, Co(mIM)₂) was synthesized. It did not introduce specific functional groups, such as -SH and -NH₂, into its structure through complicated steps. It separate Hg²⁺ from wastewater with a new strategy, which utilized the stronger coordination ability of Hg²⁺ with the nitrogen atom on the imidazole ring of the organic ligand than the Co²⁺ ions. Hg²⁺ replaced Co²⁺ nodes from ZIF-67 and formed a more stable precipitate with mIM. The experimental results showed that this new strategy was efficient. ZIF-67 exhibited Hg²⁺ adsorption capacity of 1740 mg/g, much higher than the known MOFs sorbents. mIMs is the reaction center and ZIF-67 can improve its utilization. The sample color faded from purple to white due to the loss of cobalt ion. It is a great feature of ZIF-67 that allows users to judge whether the sorbent is deactivated intuitively. ZIF-67 can be sustainable recycled by adding organic ligands to the solution after treatment due to its simple synthesis method at room temperature. It's a high-efficient and sustainable sorbent for Hg²⁺ separation from wastewater.