[Contamination Characteristics and Risk Assessment of Polycyclic Aromatic Compounds in Surface Dust of Suntuan Mining Area in Huaibei].

The Suntuan mining area of Huaibei is a typical coal resource mining base in the Huainan-Huaibei areas in North China. Previous environmental studies related to surface dust in coal mining areas mainly focused on heavy metals and water-soluble ions, with little research on polycyclic aromatic compounds (PACs). In this study, gas chromatography-triple tandem quadrupole mass spectrometry (GC-MS/MS) was used to determine the contents of 16 parent polycyclic aromatic hydrocarbons (16PAHs), alkyl polycyclic aromatic hydrocarbons (aPAHs), and some oxygenated polycyclic aromatic hydrocarbons (OPAHs) in surface dust from the Suntuan mining area and surrounding environment. The results showed that the ΣPACs concentration range of surface dust in the Suntuan mining area was 283.8-36852.5 µg·kg-1 (mean:4114.2 µg·kg-1). ΣaPAHs (mean:2593.8 µg·kg-1) was 2.4 times higher than Σ16PAHs (mean:1074.9 µg·kg-1), which was the main contributor to PAC pollution. The composition of 16PAHs and aPAHs in surface dust was dominated by low molecular polycyclic aromatic hydrocarbons. The average OPAH content was 445.6 µg·kg-1. At the same time, PAC pollution was mainly concentrated around the mining area and near the road of a coal gangue landfill. Based on the positive matrix factor (PMF) analysis, it was inferred that the study area was mainly affected by petroleum sources, followed by coal and biomass combustion, and traffic sources and petroleum product leakage accounted for a relatively small proportion. Based on the ratio and distribution pattern of 16PAHs and aPAHs, it was inferred that when Σ16PAHs/ΣPACs<0.25, it was mainly polluted by the coal mining area. The results of PMF combined with lifetime carcinogenic risk (ILCR) showed that there were potential carcinogenic risks for children near the study area, mainly from coal and biomass burning and coal mining. There are many coal mining areas in Huaihe River Basin in China. The results of this study can provide reference for pollution prevention and control of PACs in these coal mining areas.

Parent and alkylated polycyclic aromatic hydrocarbon emissions from coal seam fire at Wuda, Inner Mongolia, China: characteristics, spatial distribution, sources, and health risk assessment.

The Wuda coalfield in Inner Mongolia is a vital coal base in China, and it is the hardest-hit area for coal fires (spontaneous combustion of coal seams and coal gangue). Using gas chromatography-mass spectrometry, this work tested the concentration and analyzed the characteristics, distribution, sources, and health risks of polycyclic aromatic compounds (PACs) in the surface soil of the Wuda District, including the coal mine, coal fire, agricultural, and background areas. The soil of coal mine and coal fire area were heavily polluted with PACs, with mean concentrations of 9107 and 3163 µg kg-1, respectively, considerably higher than those in the agricultural (1232 µg kg-1) and background areas (710 µg kg-1). Alkyl polycyclic aromatic hydrocarbons (APAHs) were the dominant pollutants among these PACs, accounting for 60-81%. Alkyl naphthalenes and alkyl phenanthrenes are the primary pollutants in APAHs, accounting for 80-90% of the total amounts. Additionally, using the positive matrix factorization method, it can be concluded that the primary PAC sources are petrogenic sources, coal and biomass combustion, coal fires, and vehicle emissions. Finally, according to the cancer risk values of 16 PAHs, only the coal mine area showed a potential cancer risk. However, this result lacks a risk assessment of APAHs and underestimates the actual risk. The results of this study improved the understanding of PAC pollution in coal fire and surrounding areas and provided a reference for environmental and health risk investigations.

Distribution pattern of polycyclic aromatic compounds in coal gangue from coal city-East China.

Coal gangue is a by-product of coal, the output of which is as high as 30% of raw coal, whereas only 30% of it is recycled. The leftover remains in the environment from gangue backfilling areas and overlap with residential, agricultural, and industrial areas. Coal gangue accumulated in the environment is easily weathered and oxidized and becomes a source of various pollutants. In this paper, 30 coal gangue samples (fresh and weathered coal gangues) were collected from three mine areas in Huaibei, Anhui province, China. Gas chromatography-triple quadrupole mass spectrometry (GC-MS/MS) was used to qualitatively and quantitatively analyze thirty polycyclic aromatic compounds (PACs), including 16 polycyclic aromatic hydrocarbons (16PAHs), preferentially controlled by the United States Environmental Protection Agency (US EPA), and the corresponding alkylated polycyclic aromatic hydrocarbons (a-PAHs). The results showed that PACs existed objectively in coal gangue, and the content of a-PAHs was higher than that of 16PAHs (average values for 16PAHs ranged from 77.8 to 581 ng/g; average values for a-PAHs ranged from 97.4 to 3179 ng/g). Moreover, coal types not only affected the content and type of PACs but also affected the distribution pattern of a-PAHs at different substitution sites. With the increase of gangue weathering degree, the composition of a-PAHs kept changing; the low ring a-PAHs were more easily diffused to the environment, and the high ring a-PAHs remained enriched in the weathered coal gangue. The correlation analysis showed that the correlation between fluoranthene (FLU) and alkylated fluoranthene (a-FLU) was as high as 94%, and the calculated ratios were not more than 1.5. The basic conclusion is that not only 16PAHs and a-PAHs objectively existed in the coal gangue, but also the characteristic compound belonging to the pollution source of coal gangue oxidation have been discovered. The results of the study provide a new perspective for the analysis of existing pollution sources.

Contamination characteristics of polycyclic aromatic compounds from coal sources in typical coal mining areas in Huaibei area, China.

The Huaibei area is rich in coal resources and serves as the main energy production base in East China. However, serious environmental consequences are associated with coal mining and utilization. With increasing reports on distribution and risks by polycyclic aromatic compounds (PACs), the potential pollution of coal sources must be addressed. Here, the PAC concentrations in the topsoil, coal, and coal gangue of a typical coal mining area in Huaibei were evaluated. The mean ΣPACs in topsoil, coal, and coal gangue were 1528.3, 274,815.8, and 10,908.3 µg·kg-1, respectively. Alkyl polycyclic aromatic hydrocarbons (aPAHs) were identified as primary contributors to PACs, and the concentrations of oxygenated PAHs (oPAHs) were significantly higher in coal and coal gangue than in topsoil. PAC pollution was mainly concentrated in the coal mine area and near the coal gangue landfill road. Not only sixteen high priority pollutant PAHs (16PAHs), but PAH derivatives also contributed to the organic pollution from coal sources. Principal components analysis, multiple linear regression, characteristic ratios, and positive matrix factor analysis were used to trace PAC sources. The characteristic ratios for organic pollution from coal and gangue particles involving 16PAHs, aPAHs, and oPAHs were proposed. Further, the high-ring 16PAH ratio was also found suitable for coal mining areas. The Monte-Carlo risk assessment showed that coal particles were highly carcinogenic, and despite the low carcinogenicity of coal gangue and topsoil, they might also serve as potential carcinogens. This study aimed to disseminate knowledge on PACs from coal and coal gangue, provide a useful background for efficient resource utilization of coal gangue, and a reference for tracing PAC sources in coal mine environment media.

Dissolution of harmful trace elements from coal and the environmental risk to mine water utilization.

Under the pressure of water shortages, coal mine water has been allocated as a national water resource in China. However, the existence of harmful trace elements (HTEs) in coal mine water causes environmental risks and health concerns over its reuse. Through a lixiviation experiment, the dominant factors affecting the dissolution of HTEs in coal were simulated and analyzed, and the environmental risks of HTEs in coal mine water in China were evaluated for the first time. The average dissolved content levels of HTEs from coal were Mn > Cu > Zn > Ni > Ba > Cr > Co > V > Mo > Se > U > Pb > Cd, and the average maximum dissolution rates were Ni > Co > Mo > Zn > Cu > Cd > Mn > Se > Ba > Cr > U > Pb > V. Oxidation-reduction potential (Eh) and pH are the dominant factors controlling HTE dissolution. Higher oxygen exposure levels induce Eh and pH development, resulting in more HTE dissolution. This study constructed the dissolution potential index (FC) of HTEs from coal. Based on the results of the FC model, the areas with the highest migration potential and environmental risk of HTEs from coal seams to mine water are located in southern China, especially in the southwest, followed by areas of eastern Inner Mongolia and Shanxi and Shaanxi provinces. The corresponding risks in other regions are relatively low; thus, mine water utilization remains an effective option. This study provides an effective reference for the analysis of HTE enrichment in coal mine water and an evaluation of its safe utilization.

Contamination characteristics of alkyl polycyclic aromatic hydrocarbons in dust and topsoil collected from Huaibei Coalfield, China.

Alkyl polycyclic aromatic hydrocarbons (APAHs) are more toxic and persistent than their parent compounds. In this study, the concentrations of polycyclic aromatic compounds (PACs) in dust, topsoil and coal gangue from Huaibei Coal mine, China were analyzed by gas chromatography-mass spectrometry, confirming APAHs were the dominant pollutants. The mean concentrations of APAHs were substantially higher than those of 16 PAHs in both dust and topsoil. The mean concentration of APAHs in dust was 9197 µg kg-1, accounting for 80% of the total mean concentration of PACs. The mean concentration of APAHs in topsoil was 2835 µg kg-1, accounting for 77% of the mean concentration of PACs. Alkyl naphthalenes and alkyl phenanthrenes were the primary pollutants in APAHs. Their mean concentrations in dust and topsoil were 7782 µg kg-1 and 2333 µg kg-1, respectively. This accounted for 85% and 82% of the concentration of APAHs, respectively. Additionally, low-molecular-weight APAHs dominated the PACs of the coal mine, exhibiting petrogenic characteristics; distribution of C1-C4 NAP and C1-C4 PHE exhibited "bell shape" pattern indicated as petrogenic source. Source identification indicated that the PACs were mainly derived from petrogenic sources and vehicle emissions, followed by biomass and coal burning. Fingerprinting information of dust and topsoil were consistent with coal gangue, indicating that PACs are most likely derived from coal gangue. Coalfields comparable to our study area are widely distributed in China. Therefore, investigating PAC pollution derived from coal gangue warrants further attention.

Alkylated Polycyclic Aromatic Hydrocarbons Are the Largest Contributor to Polycyclic Aromatic Compound Concentrations in the Topsoil of Huaibei Coalfield, China.

Alkyl polycyclic aromatic hydrocarbons (APAHs) are more toxic and persistent than their parent compounds. Here, the concentrations, composition profiles, and spatial distribution of polycyclic aromatic compounds (PACs) in 127 topsoil samples from Huaibei coalfield were analyzed. The PAC concentrations in different functional areas were significantly different: mining area > industrial area > residential area > agricultural area. APAHs were the major contributors to PACs, accounting for 71-83% of total PACs. Alkylnaphthalenes and alkylphenanthrenes were the primary APAH components, accounting for 83-87% of APAHs. Principal component analysis showed that petrogenic source, coal and biomass combustion, and vehicle emissions were the primary sources of PACs. By comparing the fingerprint information of soil, coal, and coal gangue, it was hypothesized that the petrogenic source of PAC pollution in typical mining areas and surrounding areas are coal particle scattering and coal gangue weathering. Some coal mining and industrial areas potentially pose risks to children, whereas others do not. There are limited evaluation criteria for alkyl PAHs; hence, the estimated risk is likely lower than the actual risk. In addition to the conventional 16 PAHs, it is critical to consider a broader range of PACs, especially APAHs.

Concentration and speciation of mercury in atmospheric particulates in the Wuda coal fire area, Inner Mongolia, China.

Coal-seam fire is a source of atmospheric mercury that is difficult to control. The Wuda Coalfield in Inner Mongolia, China, is one of the most severe coal fire disaster areas worldwide and has been burning for more than 50 years. To investigate atmospheric mercury pollution from the Wuda coal fire, gaseous elemental mercury (GEM) concentrations and atmospheric particulate mercury (PHg) speciation were measured using a RA-915+ mercury analyzer and the temperature-programmed desorption method. Near-surface GEM concentrations in the Wuda Coalfield and adjacent urban area were 80 ng m-3 (65-90 ng m-3) and 52 ng m-3 (25-95 ng m-3), respectively, which are far higher than the local background value (22 ng m-3). PHg concentrations in the coalfield and urban area also reached significantly high levels, 33 ng m-3 (25-45 ng m-3) and 22 ng m-3 (14-29 ng m-3), respectively (p < 0.05). There is no clear evidence that PHg combines with organic carbon or elemental carbon, but PHg concentration appears to be controlled by air acidity. PHg mainly exists in inorganic forms, such as HgCl2, HgS, HgO, and Hg(NO3)2·H2O. This work can provide references for the speciation analysis of atmospheric PHg and the safety assessment of environmental mercury.

Study on Mercury Species in Coal and Pyrolysis-Based Mercury Removal before Utilization.

Coal-fired mercury (Hg) pollution control is an important global environmental context. Eight coal samples from different coal fields in China were used to investigate Hg species and the Hg removal effects under different pyrolysis conditions in the presence of nitrogen. These conditions included temperature, particle size, and residence time. The study concludes that the temperature is the most important factor affecting Hg removal from coal, and the mercury release activity at specific temperatures depends on the species and content of Hg present. Large particle size limits the removal rate of Hg, and coal particles smaller than 40 mesh are more favorable for the rapid removal of Hg. For most coal types, pyrolysis of 10-15 min can achieve the ultimate Hg removal effect. Rapid pyrolysis at 600 °C in nitrogen is feasible to remove Hg from coal. Consequently, the Hg removal rate reaches 88-100%, the loss rate of coal calorific value is 2-12%, and approximately 17-58% of S is removed synergistically. HgS, HgSe, HgSO4, organic matter Hg, and HgO are the main types of Hg species detected in coal, whose thermal decomposition characteristics are the essential criteria for determining the type of Hg removal process. This research will facilitate the improvement of pollution control methods for coal-source Hg pollution.

Intrinsically Stretchable, Transient Conductors from a Composite Material of Ag Flakes and Gelatin Hydrogel.

Transient conductors are one of the most important components in transient electronics, which attract great attention because of their environment-friendly and biocompatible characters. To meet the requirement for wearable electronics, good stretchability and mechanical durability are needed for the transient conductors. However, it remains challenging to achieve stretchability and transient behavior simultaneously because of a lack of the proper elastomer. Herein, we demonstrate the first highly stretchable and transient conductor from a composite material of Ag flakes and gelatin hydrogel. It shows a maximum stretchability of more than 100% with minimal resistance increase and a good cyclic durability of 1000 cycles of deformation at 20%. The above mentioned good mechanical properties come from the rational design of the conductor with a seamless interface between the hydrogel and Ag flakes. When the conductor is immersed in water at 60 °C, it can be quickly dissolved within 90 s, and the transient behavior can be controlled by tuning the content of the hydrogel in the conductors and dissolving temperature. These properties make the conductor a good wiring candidate for stretchable and transient electronics.

Enzymatic Manufacture of Deoxythymidine-5'-Triphosphate with Permeable Intact Cells of E. coli Coexpressing Thymidylate Kinase and Acetate Kinase.

A one-pot process of enzymatic synthesis of deoxythymidine-5'-triphosphate (5'-dTTP) employing whole cells of recombinant Escherichia coli coexpressing thymidylate kinase (TMKase) and acetate kinase (ACKase) was developed. Genes tmk and ack from E. coli were cloned and inserted into pET28a(+), and then transduced into E. coli BL21 (DE3) to form recombinant strain pTA in which TMKase and ACKase were simultaneously overexpressed. It was found that the relative residual specific activities of TMKase and ACKase, in pTA pretreated with 20 mM ethylene diamine tetraacetic acid (EDTA) at 25°C for 30 min, were 94% and 96%, respectively. The yield of 5'-dTTP reached above 94% from 5 mM deoxythymidine 5'-monophosphate (5'-dTMP) and 15 mM acetyl phosphate catalyzed with intact cells of pTA pretreated with EDTA. The process was so effective that only 0.125 mM adenosine-5'- triphosphate was sufficient to deliver the phosphate group from acetyl phosphate to dTMP and dTDP.

Phosphorylation of uridine and cytidine by uridine-cytidine kinase.

Uridine 5'-monophosphate (5'-UMP) and cytidine 5'-monophosphate (5'-CMP) were biosynthesized by recombinant uridine-cytidine kinase (UCK) and acetate kinase (ACK). The ack and uck genes from Escherichia coli K12 and the uck1, uck2 and ack genes from Lactobacillus bulgaricus ATCC 11842 were cloned and inserted into the plasmid pET-28a. All of the recombinant E. coli strains were capable of overexpressing UCK and ACK, which catalyzed the reaction using guanosine 5'-triphosphate (GTP) as a phosphate intermediate that was regenerated by ACK from acetyl phosphate. The effect of several parameters, including the substrate concentration, the GTP concentration, the temperature and the reaction pH, were optimized. High efficiency was achieved if uridine or cytidine was phosphorylated by UCK encoded by uck from E. coli and ACK encoded by ack from L. bulgaricus. The maximum conversion yield of 5'-UMP and 5'-CMP was 97% at 37 °C and pH 7.5 when 30 mM uridine/cytidine and 0.5mM GTP in a total of 1 mL were used. In addition, the 5'-UMP and 5'-CMP products were very stable in the reaction system and did not undergo significant degradation.