1. |
- Forgács, Gergely, 1983, et al.
(author)
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Biological treatment of chicken feather waste for improved biogas production
- 2011
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In: Journal of Environmental Sciences. - : Elsevier BV. - 1001-0742 .- 1878-7320. ; 23:10, s. 1747-1753
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Journal article (peer-reviewed)abstract
- A two-stage system was developed which combines the biological degradation of keratin-rich waste with the production of biogas. Chicken feather waste was treated biologically with a recombinant Bacillus megaterium strain showing keratinase activity prior to biogas production. Chopped, autoclaved chicken feathers (4%, W/V) were completely degraded, resulting in a yellowish fermentation broth with a level of 0.51 mg/mL soluble proteins after 8 days of cultivation of the recombinant strain. During the subsequent anaerobic batch digestion experiments, methane production of 0.35 Nm(3)/kg dry feathers (i.e., 0.4 Nm(3)/kg volatile solids of feathers), corresponding to 80% of the theoretical value on proteins, was achieved from the feather hydrolyzates, independently of the pre-hydrolysis time period of 1, 2 or 8 days. Cultivation with a native keratinase producing strain, Bacillus licheniformis resulted in only 0.25 mg/mL soluble proteins in the feather hydrolyzate, which then was digested achieving a maximum accumulated methane production of 0.31 Nm(3)/kg dry feathers. Feather hydrolyzates treated with the wild type B. megaterium produced 0.21 Nm(3) CH(4)/kg dry feathers as maximum yield.
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2. |
- Ibrahim, Victor, et al.
(author)
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Determining Short Chain Fatty Acids in Sewage Sludge Hydrolysate: A Comparison of Three Analytical Methods and Investigation of Sample Storage Effects
- 2014
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In: Journal of Environmental Sciences(China). - 1001-0742. ; 26:4, s. 926-933
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Journal article (peer-reviewed)abstract
- In anaerobic digestion (AD), the production of short-chain fatty acids (SCFAs) can be beneficial or harmful to the overall process, depending on the concentration of accumulated acids. Therefore, the accurate determination of the SCFA concentration in both fresh and stored sludge hydrolysates is important. To select a suitable method for monitoring SCFAs during the AD of sewage sludge, the accuracy of three available analytical methods, including 5 pH point acid titration (TITRA5), gas chromatography (GC), and spectrophotometry, were compared in the present study. The results revealed that TITRA5 and GC displayed better agreement in the achieved measurements and higher precision and accuracy than the spectrophotometric assay, as supported by the application of different statistical models. TITRA5 excelled in titrating unfiltered hydrolysate while simultaneously measuring the alkalinity, whereas the GC method provided detailed information on the contribution of different fatty acids to the total acidity. In contrast, the spectrophotometric assay suffered from many forms of interference, depending on the sample’s matrix. SCFA production followed the pattern of enzymatic reactions and fitted the Michaelis-Menten model. In addition to promoting TITRA5 as an accurate and robust analytical tool for routine SCFA analyses, this comparative study also demonstrated the possibility of storing hydrolysate samples at different temperatures and durations without altering the SCFA measurements.
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3. |
- Shi, P., et al.
(author)
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Thermodynamic investigations on materials corrosion in some industrial and environmental processes
- 2011
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In: Journal of Environmental Sciences. - 1001-0742. ; 23:SUPPL., s. S1-S7
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Journal article (peer-reviewed)abstract
- For better understanding of corrosion schemes and corrosion mechanisms of a wide range of steels/Fe-alloys, Ni-/NiFe-/Co-superalloys, Al-/Mg-/Ti-/Zr-/Sn-/Cu-/Zn-alloys, electronic-packing alloys, medical-instrument alloys and other materials, under various corrosive environments (such as aqueous solutions, non-aqueous solutions, molten salts, high-temperature gases, etc.) during production/application processes and experimental observations, the Thermo-Calc software/database/programming-interface package can be used. This article is aimed at presenting some application examples of thermodynamic calculations/simulations in some specific areas: aqueous corrosions of stainless steels and other alloys, and of high-performance corrosion-resistant materials (HPCRM); molten salt corrosions of stainless steels and high-temperature alloys; high-temperature gaseous corrosions of steels/alloys; formations of oxide-coated protective layers on steel/alloy surfaces; and emergence conditions during oxidation of steels/alloys.
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4. |
- Yang, Weijin, et al.
(author)
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Alterations of endogenous metabolites in urine of rats exposed to decabromodiphenyl ether using metabonomic approaches
- 2014
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In: Journal of Environmental Sciences(China). - : Elsevier. - 1001-0742 .- 1878-7320. ; 26:4, s. 900-908
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Journal article (peer-reviewed)abstract
- There is large usage of polybrominated diphenyl ethers (PBDEs) especially for decabromodiphenyl ether (BDE-209, Deca-BDE) in controlling the risks of fire. The toxicological effects of PBDEs are worth being concerned about. Female SD rats were daily gavaged with BDE-209 ether at the dose of 100 mg/kg for 20 days. Histological observation was performed for the screening of the target organs for BDE-209 exposure. The distribution and metabolism of PBDEs in the exposed main organs were evidenced by HRGC-HRMS. Alterations of the endogenous metabolite concentrations in urine were investigated using metabonomic approaches based on (1)H NMR spectrum. Histopathological changes including serious edema in kidney, hepatocellular spotty necrosis and perivasculitis in liver indicated that BDE-209 caused potential influences on endogenous metabolism in the exposed liver and the kidney. BDE-209 was found to be highly accumulated in lipid, ovary, kidney and liver after 20 days' exposure. Occurrence of other lower brominated PBDEs in the rats demonstrated that reductive debromination process happened in vivo. Hydroxylated and methoxylated-BDEs, as metabolism products, were also detected in the rat tissues. A total of 12 different endogenous metabolites showed obvious alterations in urine from the exposed rats, indicating the disturbance of the corresponding internal biochemical processes induced by BDE-209 exposure. These findings in vivo suggested the potential health risk might be of concern due to the toxicological effects of BDE-209 as a ubiquitous compound in the environment.
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5. |
- Wang, Zengzhang, et al.
(author)
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Management of process performance at low water temperatures in respect of filamentous organisms
- 2004
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In: Journal of Environmental Sciences(China). - 1001-0742 .- 1878-7320. ; 16:1, s. 113-116
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Journal article (peer-reviewed)abstract
- The management of sludge-settling properties in Nordic conditions is of importance during the low temperature (spring) season because of the peak settler load. A survey was made in 10 Finnish waste water treatment plants(WWTP's) and the total extended filament length and DSVI in half of the plants exceeded the limits, which indicates sludge bulking(15 km/g SS and 150 ml/g respectively). The dominant organism was Microthrix parvicella, the abundance of which was 59.22% of total extended filament length on average. Chemicals were tested to control the filaments, and it was found that special attention has to be paid to maintaining the nitrification at low temperature. A dosage of(H2O2-based) oxidants controlled the growth of Microthrix parvicella effectively and rapidly, whereas with the use of aluminium hydroxidechloride a 2 to 5-week period was needed to decrease the filament length.
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6. |
- Eriksson, Ulrika, 1972-, et al.
(author)
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Contribution of precursor compounds to the release of per- and polyfluoroalkyl substances (PFASs) from waste water treatment plants (WWTPs)
- 2017
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In: Journal of Environmental Sciences(China). - : SCIENCE PRESS. - 1001-0742 .- 1878-7320. ; 61, s. 80-90
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Journal article (peer-reviewed)abstract
- Per- and polyfluoroalkyl substances (PFASs) are ubiquitous in sludge and water from waste water treatment plants, as a result of their incorporation in everyday products and industrial processes. In this study, we measured several classes of persistent PFASs, precursors, transformation intermediates, and newly identified PFASs in influent and effluent sewage water and sludge from three municipal waste water treatment plants in Sweden, sampled in 2015. For sludge, samples from 2012 and 2014 were analyzed as well. Levels of precursors in sludge exceeded those of perfluoroalkyl acids and sulfonic acids (PFCAs and PFSAs), in 2015 the sum of polyfluoroalkyl phosphoric acid esters (PAPs) were 15-20 ng/g dry weight, the sum of fluorotelomer sulfonic acids (FTSAs) was 0.8-1.3 ng/g, and the sum of perfluorooctane sulfonamides and ethanols ranged from non-detected to 3.2 ng/g. Persistent PFSAs and PFCAs were detected at 1.9-3.9 ng/g and 2.4-7.3 ng/g dry weight, respectively. The influence of precursor compounds was further demonstrated by an observed substantial increase for a majority of the persistent PFCAs and PFSAs in water after waste water treatment. Perfluorohexanoic acid (PFHxA), perfluorooctanoic acid (PFOA), perfluorohexane sulfonic acid (PFHxS), and perfluorooctane sulfonic acid (PFOS) had a net mass increase in all WWTPs, with mean values of 83%, 28%, 37% and 58%, respectively. The load of precursors and intermediates in influent water and sludge combined with net mass increase support the hypothesis that degradation of precursor compounds is a significant contributor to PFAS contamination in the environment. (C) 2017 The Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V.
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7. |
- Gao, Guangbin, et al.
(author)
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Understanding filamentous cyanobacteria and their adaptive niches in Lake Honghu, a shallow eutrophic lake
- 2025
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In: Journal of Environmental Sciences (China). - 1001-0742. ; 152, s. 219-234
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Journal article (peer-reviewed)abstract
- Freshwater lakes globally are witnessing an escalation in the frequency and intensity of cyanobacterial harmful blooms. However, underlying factors influencing the succession or coexistence of cyanobacteria, especially filamentous ones, remain poorly understood. Lake Honghu, a Ramsar Wetland of International Importance with degrading aquatic ecological quality, served as a case study to elucidate the intricate relationship between environmental changes and cyanobacterial dynamics. Our analysis revealed a significant increase in the dominance of filamentous cyanobacteria, marked by high spatiotemporal variability in community structure. This dominance of filamentous diazotrophic cyanobacteria is attributed to a decrease in the ratio of dissolved inorganic nitrogen to total phosphorus and their capacity to utilize organic phosphorus in phosphorus-deficient conditions. Species-specific density variations were linked to diverse environmental factors, with total nitrogen or total phosphorus concentration remaining as a crucial factor influencing dominant cyanobacterial density fluctuations. The dominance of low-temperature-tolerant Aphanizomenon and Pseudanabaena was evident in spring and winter, whereas Dolichospermum and Cylindrospermopsis, which prefer higher temperatures, thrived in summer and autumn. Additionally, non-algal turbidity and heterogeneity can potentially alter the competitive outcome among filamentous cyanobacteria or foster coexistence under conditions of elevated temperatures and nutrient limitation. This study predicts that filamentous cyanobacteria may spread and persist in lakes spanning a wide trophic range. Current findings enhance our comprehension of the dynamic responses exhibited by filamentous bloom-forming cyanobacteria in the face of environmental changes within shallow eutrophic lakes and provide valuable insights for lake managers involved in the remediation of degraded shallow lakes.
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8. |
- González-Arias, Judith, et al.
(author)
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Hydrochar and synthetic natural gas co-production for a full circular economy implementation via hydrothermal carbonization and methanation: An economic approach
- 2024
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In: Journal of Environmental Sciences. - 1001-0742 .- 1878-7320. ; 140, s. 69-78
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Journal article (peer-reviewed)abstract
- Herein we study the economic performance of hydrochar and synthetic natural gas co-production from olive tree pruning. The process entails a combination of hydrothermal carbonization and methanation. In a previous work, we evidenced that standalone hydrochar production via HTC results unprofitable. Hence, we propose a step forward on the process design by implementing a methanation, adding value to the gas effluent in an attempt to boost the overall process techno-economic aspects. Three different plant capacities were analyzed (312.5, 625 and 1250 kg/hr). The baseline scenarios showed that, under the current circumstances, our circular economy strategy in unprofitable. An analysis of the revenues shows that hydrochar selling price have a high impact on NPV and subsidies for renewable coal production could help to boost the profitability of the process. On the contrary, the analysis for natural gas prices reveals that prices 8 times higher than the current ones in Spain must be achieved to reach profitability. This seems unlikely even under the presence of a strong subsidy scheme. The costs analysis suggests that a remarkable electricity cost reduction or electricity consumption of the HTC stage could be a potential strategy to reach profitability scenarios. Furthermore, significant reduction of green hydrogen production costs is deemed instrumental to improve the economic performance of the process. These results show the formidable techno-economic challenge that our society faces in the path towards circular economy societies.
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9. |
- Gu, S., et al.
(author)
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Anthropogenic land use substantially increases riverine CO2 emissions
- 2022
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In: Journal of Environmental Sciences (China). - : Elsevier BV. - 1001-0742. ; 118, s. 158-170
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Journal article (peer-reviewed)abstract
- Carbon dioxide (CO2) emissions from inland waters to the atmosphere are a pivotal component of the global carbon budget. Anthropogenic land use can influence riverine CO2 emissions, but empirical data exploring cause-effect relationships remain limited. Here, we investigated CO2 partial pressures (pCO2) and degassing in a monsoonal river (Yue River) within the Han River draining to the Yangtze in China. Almost 90% of river samples were supersaturated in CO2 with a mean ± standard deviation of 1474 ± 1614 µatm, leading to emissions of 557 - 971 mmol/m2/day from river water to the atmosphere. Annual CO2 emissions were 1.6 - 2.8 times greater than the longitudinal exports of riverine dissolved inorganic and organic carbon. pCO2 was positively correlated to anthropogenic land use (urban and farmland), and negatively correlated to forest cover. pCO2 also had significant and positive relationships with total dissolved nitrogen and total dissolved phosphorus. Stepwise multiple regression models were developed to predict pCO2. Farmland and urban land released nutrients and organic matter to the river system, driving riverine pCO2 enrichment due to enhanced respiration in these heterotrophic rivers. Overall, we show the crucial role of land use driving riverine pCO2, which should be considered in future large-scale estimates of CO2 emissions from streams. Land use change can thus modify the carbon balance of urban-river systems by enhancing river emissions, and reforestation helps carbon neutral in rivers. © 2022
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10. |
- Gu, Zhenhong, et al.
(author)
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Analysis of the most widely used building environmental assessment methods
- 2006
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In: Journal of Environmental Sciences(China). - : Informa UK Limited. - 1001-0742 .- 1878-7320. ; 3:3, s. 175-192
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Journal article (peer-reviewed)abstract
- Building Environmental Assessment (BEA) is a term used for several methods for environmental assessment of the building environment. Generally, Life Cycle Assessment (LCA) is an important foundation and part of the BEA method, but current BEA methods form more comprehensive tools than LCA. Indicators and weight assignments are the two most important factors characterizing BEA. From the comparison of the three most widely used BEA methods, EcoHomes (BREEAM for residential buildings), LEED-NC and GBTool, it can be seen that BEA methods are shifting from ecological, indicator-based scientific systems to more integrated systems covering ecological, social and economic categories. Being relatively new methods, current BEA systems are far from perfect and are under continuous development. The further development of BEA methods will focus more on non-ecological indicators and how to promote implementation. Most BEA methods are developed based on regional regulations and LCA methods, but they do not attempt to replace these regulations. On the contrary, they try to extend implementation by incentive programmes. There are several ways to enhance BEA in the future: expand the studied scope from design levels to whole life-cycle levels of constructions, enhance international cooperation, accelerate legislation and standardize and develop user-oriented assessment systems.
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11. |
- Jiang, Tao
(author)
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Linking the electron donation capacity to the molecular composition of soil dissolved organic matter from the Three Gorges Reservoir areas, China
- 2020
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In: Journal of Environmental Sciences. - : Elsevier BV. - 1001-0742. ; 90, s. 146-156
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Journal article (peer-reviewed)abstract
- Soil dissolved organic matter (DOM) plays an essential role in the Three Gorges Reservoir (TGR) as a linkage between terrestrial and aquatic systems. In particular, the reducing capacities of soil DOM influence the geochemistry of contaminants such as mercury (Hg). However, few studies have investigated the molecular information of soil DOM and its relationship with relevant geochemical reactivities, including redox properties. We collected samples from eight sites in the TGR areas and studied the link between the molecular characteristics of DOM and their electron donation capacities (EDCs) toward Hg(II). The average kinetic rate and EDC of soil DOM in TGR areas were (0.004 +/- 0.001) hr(-1) and (2.88 +/- 1.39) nmol e(-)/mg DOMbulk, respectively. Results suggest that higher EDCs and relatively rapid kinetics were related to the greater electron donating components of lignin-derived and perhaps pyrogenic DOM, which are the aromatic constituents that influenced the reducing capacities of DOM in the present study. Molecular details revealed that even the typical autochthonous markers are important for the EDCs of DOM as well, in contrast to what is generally assumed. More studies identifying specific DOM molecular components involved in the abiotic reduction of Hg(II) are required to further understand the relations between DOM sources and their redox roles in the environmental fate of contaminants. (C) 2019 The Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V.
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12. |
- Jiang, Tao
(author)
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Preliminary investigation of phosphorus adsorption onto two types of iron oxide-organic matter complexes
- 2016
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In: Journal of Environmental Sciences. - : Elsevier BV. - 1001-0742. ; 42, s. 152-162
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Journal article (peer-reviewed)abstract
- Iron oxide (FeO) coated by natural organic matter (NOM) is ubiquitous. The associations of minerals with organic matter (OM) significantly changes their surface properties and reactivity, and thus affect the environmental fate of pollutants, including nutrients (e.g., phosphorus (P)). In this study, ferrihydrite/goethite-humic acid (FH/GE-HA) complexes were prepared and their adsorption characteristics on P at various pH and ionic strength were investigated. The results indicated that the FeO-OM complexes showed a decreased P adsorption capacity in comparison with bare FeO. The maximum adsorption capacity (Q(max)) decreased in the order of FH (22.17 mg/g) > FH-HA (5.43 mg/g) > GE (4.67 mg/g) > GE-HA (3.27 mg/g). After coating with HA, the amorphous FH-HA complex still showed higher P adsorption than the crystalline GE-HA complex. The decreased P adsorption observed might be attributed to changes of the FeO surface charges caused by OM association. The dependence of P adsorption on the specific surface area of adsorbents suggests that the FeO component in the complexes is still the main contributor for the adsorption surfaces. The P adsorptions on FeO-HA complexes decreased with increasing initial pH or decreasing initial ionic strength. A strong dependence of P adsorption on ionic strength and pH may demonstrate that outer-sphere complexes between the OM component on the surface and P possibly coexist with inner-sphere surface complexes between the FeO component and P. Therefore, previous over-emphasis on the contributions of original minerals to P immobilization possibly over-estimates the P loading capacity of soils, especially in humic-rich areas. (C) 2015 The Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V.
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13. |
- Jiang, Tao
(author)
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Underestimation of phosphorus fraction change in the supernatant after phosphorus adsorption onto iron oxides and iron oxide-natural organic matter complexes
- 2017
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In: Journal of Environmental Sciences. - : Elsevier BV. - 1001-0742. ; 55, s. 197-205
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Journal article (peer-reviewed)abstract
- The phosphorus (P) fraction distribution and formation mechanism in the supematant after P adsorption onto iron oxides and iron oxide-humic acid (HA) complexes were analyzed using the ultrafiltration method in this study. With an initial P concentration of 20 mg/L (I = 0.01 mol/L and pH = 7), it was shown that the colloid (1 kDa-0.45 gm) component of P accounted for 10.6%, 11.6%, 6.5%, and 4.0% of remaining total P concentration in the supematant after P adsorption onto ferrihydrite (FH), goethite (GE), ferrihydrite-humic acid complex (FH-HA), goethite-humic acid complex (GE-HA), respectively. The <1 kDa component of P was still the predominant fraction in the supematant, and underestimated colloidal P accounted for 2.2%, 55.1%, 45.5%, and 38.7% of P adsorption onto the solid surface of FH, FH-HA, GE and GE-HA, respectively. Thus, the colloid P could not be neglected. Notably, it could be interpreted that Fe3+ hydrolysis from the adsorbents followed by the formation of colloidal hydrous ferric oxide aggregates was the main mechanism for the formation of the colloid P in the supematant. And colloidal adsorbent particles co-existing in the supernatant were another important reason for it. Additionally, dissolve organic matter dissolved from iron oxide-HA complexes could occupy large adsorption sites of colloidal iron causing less colloid P in the supematant. Ultimately, we believe that the findings can provide a new way to deeply interpret the geochemical cycling of P, even when considering other contaminants such as organic pollutants, heavy metal ions, and arsenate at the sediment/soil-water interface in the real environment. (C) 2016 The Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V.
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14. |
- Kanbar, Hussein Jaafar, et al.
(author)
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Selective metal leaching from technosols based on synthetic root exudate composition
- 2020
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In: Journal of Environmental Sciences(China). - : Science Press. - 1001-0742 .- 1878-7320. ; 96, s. 85-92
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Journal article (peer-reviewed)abstract
- This study focused on metal release from technosols induced by synthetic root exudate (SRE). The effect of SRE composition on metal release was studied using six technosols. This was done by treating the technosols with SRE solutions having varying concentrations of low molecular weight organic acids (LMWOAs), namely oxalic, citric, and malic acids. Consequently, the physico-chemical parameters (pH and electric conductivity), Ca, Mg, Fe, Zn, and Cu release (by atomic absorption spectroscopy, AAS), chemical changes (by Fourier transform infrared, FT-IR), and organic parameters (by fluorescence) were investigated. Metal release showed to be dependent on the SRE composition and technosol characteristics. Citric acid selectively released Ca, Mg, Zn, and Cu from technosols in a concentration-dependent manner; oxalic acid showed a significant role in the release of Mg and Fe. Under relatively high LMWOA concentrations, particulate organo- mineral complexes precipitated. Additionally, technosol weathering was seen by the dissolution of humic substances and ferriallophanes, which in turn caused metal release. However, re-precipitation of these phases showed to re-sorb metals, thus underestimating the role of LMWOAs in metal release. Therefore, the selective metal leaching was highly dependent on the SRE composition and LMWOA concentrations on one hand, and on the mineral, organic, and organo-mineral components of the technosols on the other. The understanding of such processes is crucial for proposing and implementing environmental management strategies to reduce metal leaching or for the beneficial re-usage of metals (e.g., for agromining) from technosols. (C) 2020 The Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V.
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15. |
- Li, S S, et al.
(author)
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Effects of temperature on UV-B-induced DNA damage and photorepair in Arabidopsis thaliana
- 2004
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In: Journal of Environmental Sciences(China). - 1001-0742. ; 16:1, s. 173-176
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Journal article (peer-reviewed)abstract
- DNA damage in the form of cyclobutane pyrimidine dimers(CPDs) and (6-4) photoproducts(6-4PPs) induced by UV-B radiation in Arabidopsis thaliana at different temperatures was investigated using ELISA with specific monoclonal antibodies. CPDs and 64PPs increased during 3 h UV-B exposure, but further exposure led to decreases. Contrary to the commonly accepted view that DNA damage induced by UV-B radiation is temperature-independent because of its photochemical nature, we found UV-B-induction of CPDs and 64PPs in Arabidopsis to be slower at a low than at a high temperature. Photorepair of CPDs at 24degreesC was much faster than that at 0degreesC and 12degreesC with 50% CPDs removal during 1 h exposure to white light. Photorepair of 6-4PPs at 12degreesC was very slow as compared with that at 24degreesC and almost no removal of 6-4PPs was detected after 4 h exposure to white light at 0degreesC. There was evidence to suggest that temperature-dependent DNA damage and photorepair could have important ecological implications.
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16. |
- Lu, Xiaotian, et al.
(author)
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Climate change induced eutrophication of cold-water lake in an ecologically fragile nature reserve
- 2019
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In: Journal of Environmental Sciences (China). - : Elsevier BV. - 1001-0742 .- 1878-7320. ; 75, s. 359-369
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Journal article (peer-reviewed)abstract
- © 2018 Aquatic ecosystem sustainability around the globe is facing crucial challenges because of increasing anthropogenic and natural disturbances. In this study, the Tianchi Lake, a typical cold-water lake and a UNESCO/MAB (Man and Biosphere) nature reserve located in high latitude and elevation with the relatively low intensity of human activity was chosen as a system to examine the linkages between climate change and eutrophication. As a part of the UNESCO Bogda Man and Biosphere Reserve, Tianchi Lake has been well preserved for prevention from human intervention, but why has it been infected with eutrophication recent years? Our results show that climate change played a significant role in the eutrophication in the Tianchi Lake. Increased temperature, changed precipitation pattern and wind-induced hydrodynamic fluctuations in the summer season were suggested to make a major contribution to the accelerated eutrophication. The results also showed that the local temperature and precipitation changes were closely linked to the large-scale atmospheric circulation, which opens the door for the method to be applied in other regions without local climatic information. This study suggests that there is an urgent need to take into consideration of climate change adaptation into the conservation and management of cold-water lakes globally.
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17. |
- Meng, Qingpeng, et al.
(author)
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Zeolite A synthesized from alkaline assisted pre-activated halloysite for efficient heavy metal removal in polluted river water and industrial wastewater
- 2017
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In: Journal of Environmental Sciences(China). - : Elsevier BV. - 1001-0742 .- 1878-7320. ; 56, s. 254-262
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Journal article (peer-reviewed)abstract
- High quality zeolite A was synthesized through a hydrothermal process using alkaline-assisted pre-activated halloysite mineral as the alumina and silica source. The synthesis conditions employed in this study were finely tuned by varying the activating temperature, sodium hydroxide content, water content and Si/Al ratio. The obtained zeolite A showed excellent adsorption properties for both single metal cation solutions and mixed cation solutions when the concentrations of the mixed cations were comparable with those in polluted natural river water and industrial wastewater. High adsorptive capacities for Ag+ (123.05 mg/g) and Pb2+ (227.70 mg/g) were achieved using the synthesized zeolite A. This observation indicates that the zeolite A synthesized from alkaline-assisted pre-activated halloysite can be used as a low-cost and relatively effective adsorbent to purify heavy metal cation polluted natural river water and industrial wastewater.
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18. |
- Morin, Nicolas A. O., et al.
(author)
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The presence and partitioning behavior of flame retardants in waste, leachate, and air particles from Norwegian waste-handling facilities
- 2017
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In: Journal of Environmental Sciences(China). - : Science Press. - 1001-0742 .- 1878-7320. ; 62, s. 115-132
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Journal article (peer-reviewed)abstract
- Flame retardants in commercial products eventually make their way into the waste stream. Herein the presence of flame retardants in Norwegian landfills, incineration facilities and recycling sorting/defragmenting facilities is investigated. These facilities handled waste electrical and electronic equipment (WEEE), vehicles, digestate, glass, combustibles, bottom ash and fly ash. The flame retardants considered included polybrominated diphenyl ethers (∑ BDE-10) as well as dechlorane plus, polybrominated biphenyls, hexabromobenzene, pentabromotoluene and pentabromoethylbenzene (collectively referred to as ∑ FR-7). Plastic, WEEE and vehicles contained the largest amount of flame retardants (∑ BDE-10: 45,000–210,000 μg/kg; ∑ FR-7: 300–13,000 μg/kg). It was hypothesized leachate and air concentrations from facilities that sort/defragment WEEE and vehicles would be the highest. This was supported for total air phase concentrations (∑ BDE-10: 9000–195,000 pg/m3 WEEE/vehicle facilities, 80–900 pg/m3 in incineration/sorting and landfill sites), but not for water leachate concentrations (e.g., ∑ BDE-10: 15–3500 ng/L in WEEE/Vehicle facilities and 1–250 ng/L in landfill sites). Landfill leachate exhibited similar concentrations as WEEE/vehicle sorting and defragmenting facility leachate. To better account for concentrations in leachates at the different facilities, waste-water partitioning coefficients, Kwaste were measured (for the first time to our knowledge for flame retardants). WEEE and plastic waste had elevated Kwaste compared to other wastes, likely because flame retardants are directly added to these materials. The results of this study have implications for the development of strategies to reduce exposure and environmental emissions of flame retardants in waste and recycled products through improved waste management practices.
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19. |
- Myrstener, Maria, et al.
(author)
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The effects of temperature and resource availability on denitrification and relative N2O production in boreal lake sediments
- 2016
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In: Journal of Environmental Sciences(China). - : Elsevier. - 1001-0742 .- 1878-7320. ; 47, s. 82-90
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Journal article (peer-reviewed)abstract
- Anthropogenic environmental stressors (like atmospheric deposition, land use change, and climate warming) are predicted to increase inorganic nitrogen and organic carbon loading to northern boreal lakes, with potential consequences for denitrification in lakes. However, our ability to predict effects of these changes is currently limited as northern boreal lakes have been largely neglected in denitrification studies. The aim of this study was therefore to assess how maximum potential denitrification and N2O production rates, and the relationship between the two (relative N2O production), is controlled by availability of nitrate (NO3−), carbon (C), phosphorus (P), and temperature. Experiments were performed using the acetylene inhibition technique on sediments from a small, nutrient poor boreal lake in northern Sweden in 2014. Maximum potential denitrification and N2O production rates at 4°C were reached already at NO3− additions of 106–120 μg NO3−–N/L, and remained unchanged with higher NO3 amendments. Higher incubation temperatures increased maximum potential denitrification and N2O production rates, and Q10 was somewhat higher for N2O production (1.77) than for denitrification (1.69). The relative N2O production ranged between 13% and 64%, and was not related to NO3− concentration, but the ratio increased when incubations were amended with C and P (from a median of 16% to 27%). Combined, our results suggests that unproductive northern boreal lakes currently have low potential for denitrification but are susceptible to small changes in NO3 loading especially if these are accompanied by enhanced C and P availability, likely promoting higher N2O production relative to N2.
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20. |
- Pagés Díaz, Jhosané, et al.
(author)
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A comparison of process performance during the anaerobic mono-and co-digestion of slaughter house waste through different operational modes
- 2017
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In: Journal of Environmental Sciences(China). - : Elsevier BV. - 1001-0742 .- 1878-7320.
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Journal article (peer-reviewed)abstract
- The use of consecutive feeding was applied to investigate the response of the microbial biomass to a second addition of substrates in terms of biodegradation using batch tests as a promising alternative to predict the behavior of the process. Anaerobic digestion (AD) of the slaughterhouse waste (SB) and its co-digestion with manure (M), various crops (VC), and municipal solid waste were evaluated. The results were then correlated to previous findings obtained by the authors for similar mixtures in batch and semi-continuous operation modes. AD of the SB failed showing total inhibition after a second feeding. Co-digestion of the SB + M showed a significant improvement for all of the response variables investigated after the second feeding, while co-digestion of the SB + VC resulted in a decline in all of these response variables. Similar patterns were previously detected, during both the batch and the semi-continuous modes.
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21. |
- Pan, Yitao, et al.
(author)
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Dietary exposure to di-isobutyl phthalate increases urinary 5-methyl-2'-deoxycytidine level and affects reproductive function in adult male mice
- 2017
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In: Journal of Environmental Sciences(China). - : Elsevier. - 1001-0742 .- 1878-7320. ; 61, s. 14-23
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Journal article (peer-reviewed)abstract
- Phthalates are a large family of ubiquitous environmental pollutants suspected of being endocrine disruptors. Epidemiological studies have associated phthalate metabolites with decreased reproductive parameters and linked phthalate exposure with the level of urinary 5-methyl-2'-deoxycytidine (5mdC, a product of methylated DNA). In this study, adult male mice were exposed to 450mg di-isobutyl phthalate (DiBP)/(kg·day) via dietary exposure for 28days. Mono-isobutyl phthalate (MiBP, the urinary metabolite) and reproductive function parameters were determined. The levels of 5mdC and 5-hydroxymethyl-2'-deoxycytidine (5hmdC) were measured in urine to evaluate if their contents were also altered by DiBP exposure in this animal model. Results showed that DiBP exposure led to a significant increase in the urinary 5mdC level and significant decreases in sperm concentration and motility in the epididymis, accompanied with reduced testosterone levels and down-regulation of the P450 cholesterol side-chain cleavage enzyme (P450scc) gene in the mice testes. Our findings indicated that exposure to DiBP increased the urinary 5mdC levels, which supported our recent epidemiological study about the associations of urinary 5mdC with phthalate exposure in the male human population. In addition, DiBP exposure impaired male reproductive function, possibly by disturbing testosterone levels; P450scc might be a major steroidogenic enzyme targeted by DiBP or other phthalates.
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22. |
- Qiao, K., et al.
(author)
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Size-resolved effective density of submicron particles during summertime in the rural atmosphere of Beijing, China
- 2018
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In: Journal of Environmental Sciences. - : Elsevier BV. - 1001-0742. ; 73, s. 69-77
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Journal article (peer-reviewed)abstract
- Particle density is an important physical property of atmospheric particles. The information on high time-resolution size-resolved particle density is essential for understanding the atmospheric physical and chemical aging processes of aerosols particles. In the present study, a centrifugal particle mass analyzer (CPMA) combined with a differential mobility analyzer (DMA) was deployed to determine the size-resolved effective density of 50 to 350 nm particles at a rural site of Beijing during summer 2016. The measured particle effective densities decreased with increasing particle sizes and ranged from 1.43 to 1.55 g/cm(3), on average. The effective particle density distributions were dominated by a mode peaked at around 1.5 g/cm(3) for 50 to 350 nm particles. Extra modes with peaks at 1.0, 0.8, and 0.6 g/cm(3) for 150, 240, and 350 nm particles, which might be freshly emitted soot particles, were observed during intensive primary emissions episodes. The particle effective densities showed a diurnal variation pattern, with higher values during daytime. A case study showed that the effective density of Aitken mode particles during the new particle formation (NPF) event decreased considerably, indicating the significant contribution of organics to new particle growth. (C) 2018 The Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V.
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23. |
- Saqib, Naeem, 1984-, et al.
(author)
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Distribution and leaching characteristics of trace elements in ashes as a function of different waste fuels and incineration technologies
- 2015
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In: Journal of Environmental Sciences(China). - : Science Press. - 1001-0742 .- 1878-7320. ; 36:1 Oct., s. 9-21
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Journal article (peer-reviewed)abstract
- Impact of waste fuels (virgin/waste wood, mixed biofuel (peat, bark, wood chips) industrial, household, mixed waste fuel) and incineration technologies on partitioning and leaching behavior of trace elements has been investigated. Study included 4 grate fired and 9 fluidized boilers. Results showed that mixed waste incineration mostly caused increased transfer of trace elements to fly ash; particularly Pb/Zn. Waste wood incineration showed higher transfer of Cr, As and Zn to fly ash as compared to virgin wood. The possible reasons could be high input of trace element in waste fuel/change in volatilization behavior due to addition of certain waste fractions. The concentration of Cd and Zn increased in fly ash with incineration temperature. Total concentration in ashes decreased in order of Zn > Cu > Pb > Cr > Sb > As > Mo. The concentration levels of trace elements were mostly higher in fluidized boilers fly ashes as compared to grate boilers (especially for biofuel incineration). It might be attributed to high combustion efficiency due to pre-treatment of waste in fluidized boilers. Leaching results indicated that water soluble forms of elements in ashes were low with few exceptions. Concentration levels in ash and ash matrix properties (association of elements on ash particles) are crucial parameters affecting leaching. Leached amounts of Pb, Zn and Cr in > 50% of fly ashes exceeded regulatory limit for disposal. 87% of chlorine in fly ashes washed out with water at the liquid to solid ratio 10 indicating excessive presence of alkali metal chlorides/alkaline earths.
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24. |
- Uwayezu, Jean-Noel, et al.
(author)
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Sorption of Perfluorooctane sulfonate (PFOS) including its isomers on hydrargillite as a function of pH, humic substances and Na2SO4
- 2022
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In: Journal of Environmental Sciences(China). - : Elsevier. - 1001-0742 .- 1878-7320. ; 111, s. 263-272
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Journal article (peer-reviewed)abstract
- Perfluorooctane sulfonate (PFOS) is a persistent organic pollutant (POP) and emergent contaminant that are widespread in the environment. Understanding the mechanisms controlling the distribution of PFOS and its isomers between hydrargillite and the water phase is important in order to study their redistribution and mobility in the environment. This study investigated the effects of pH, humic acid, fulvic acid and Na2SO4 on sorption of PFOS isomers to hydrargillite. A mixture of PFOS isomers was spiked into water and hydrargillite was added to the system and shaken for one day; the system was tested with different aqueous composition. Concentrations of PFOS isomers in the aqueous phase were quantified using an ultra-performance liquid chromatograph coupled to a triple quadrupole mass spectrometer. Our results showed that the distribution coefficients of PFOS isomers were found to be 0.76, 0.71, 0.93 and 0.90 at pH 6.5, for 3-/4-/5- PFOS, 6-/2-PFOS, L-PFOS and total PFOS respectively. The distribution coefficients increased at lower pH and decreased at alkaline conditions. The presence of humic substances (HS) increased the sorption slightly at the environmental pH of 6.5, although a competition effect was observed during acidic conditions. A tendency of PFOS distribution to hydrargillite in the presence of Na2SO4 was like its behavior in the presence of HS although the mechanisms behind the sorption were interpreted differently. This study revealed that L-PFOS was readily sorbed when no other chemicals were added or in 20 mg/L FA or 100 mg/L Na2SO4. We suggest that an increase in PFOS sorption in the presence of HS may be due to hydrophobic mechanisms while Na2SO4 contributed to increased sorption through ionic strength effects.
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25. |
- Wang, Chao, et al.
(author)
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Characterization and sources of childhood PAEs exposure from residential airborne dust in China cities
- 2025
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In: Journal of Environmental Sciences(China). - : Elsevier. - 1001-0742 .- 1878-7320. ; 152, s. 1-13
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Journal article (peer-reviewed)abstract
- To explore the multicenter characteristics of endocrine-like phthalate esters (PAEs) in household dust and propose effective control strategies for global indoor public health. An on-site observational investigation was conducted in nine Chinese cities from 2018 to 2019. A total of 246 household dust samples were collected and analyzed for ten PAE congeners using Gas Chromatography-Mass Spectrometry (GC-MS). Questionnaires were used to gather information on building conditions, indoor behaviors, and ventilation habits. In residential dust from the nine cities, the total concentrations of the ten PAE congeners (∑PAEs) ranged from 0.921 to 29097.297 µg/g. Dicyclohexyl phthalate (DCHP) and di (2-ethylhexyl) phthalate (DEHP) were the dominant congeners in ∑PAEs. Childhood exposure to PAEs through dust ingestion was four orders of magnitude higher than through inhalation, with a carcinogenic risk of 5.47 × 10−6 for DEHP exposure in household dust. Higher ∑PAEs concentrations were associated with higher temperature, double glazing, wall paint usage, television and computer use, and indoor plant growth. This multicenter on-site investigation confirmed PAE pollution characteristics and uncovered the inacceptable risk of daily DEHP exposure in household dust under real living conditions. Effective mitigation measures based on household-related information, residential characteristics, decoration materials, and lifestyle should be taken to build a healthy household environment.
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26. |
- Wang, H., et al.
(author)
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Secondary organic aerosol formation from straw burning using an oxidation flow reactor
- 2022
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In: Journal of Environmental Sciences (China). - : Elsevier BV. - 1001-0742. ; 114, s. 249-258
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Journal article (peer-reviewed)abstract
- Herein, we use an oxidation flow reactor, Gothenburg: Potential Aerosol Mass (Go: PAM) reactor, to investigate the secondary organic aerosol (SOA) formation from wheat straw burning. Biomass burning emissions are exposed to high concentrations of hydroxyl radicals (OH) to simulate processes equivalent to atmospheric oxidation of 0-2.55 days. Primary volatile organic compounds (VOCs) were investigated, and particles were measured before and after the Go: PAM reactor. The influence of water content (i.e. 5% and 11%) in wheat straw was also explored. Two burning stages, the flaming stage, and non-flaming stages, were identified. Primary particle emission factors (EFs) at a water content of 11% (∼3.89 g/kg-fuel) are significantly higher than those at a water content of 5% (∼2.26 g/kg-fuel) during the flaming stage. However, the water content showed no significant influence at the non-flaming stage. EFs of aromatics at a non-flaming stage (321.8±46.2 mg/kg-fuel) are larger than that at a flaming stage (130.9±37.1 mg/kg-fuel). The OA enhancement ratios increased with the increase in OH exposure at first and decreased with the additional increment of OH exposure. The maximum OA enhancement ratio is ∼12 during the non-flaming stages, which is much higher than ∼ 1.7 during the flaming stages. The mass spectrum of the primary wheat burning organic aerosols closely resembles that of resolved biomass burning organic aerosols (BBOA) based on measurements in ambient air. Our results show that large gap (∼60%-90%) still remains to estimate biomass burning SOA if only the oxidation of VOCs were included. © 2021
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27. |
- Yang, Xiaofang, et al.
(author)
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Effect of phosphate on heterogeneous Fenton oxidation of catechol by nano-Fe3O4 : Inhibitor or stabilizer?
- 2016
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In: Journal of Environmental Sciences(China). - : Elsevier BV. - 1001-0742 .- 1878-7320. ; 39, s. 69-76
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Journal article (peer-reviewed)abstract
- The effect of phosphate on adsorption and oxidation of catechol, 1,2-dihydroxybenzene, in a heterogeneous Fenton system was investigated. In situ attenuated total reflectance infrared spectroscopy (ATR-FTIR) was used to monitor the surface speciation at the nano-Fe3O4 catalyst surface. The presence of phosphate decreased the removal rate of catechol and the abatement of dissolved organic compounds, as well as the decomposition of H2O2. This effect of phosphate was mainly due to its strong reaction with surface sites on the iron oxide catalyst. At neutral and acid pH, phosphate could displace the adsorbed catechol from the surface of catalyst and also could compete for surface sites with H2O2. In situ IR spectra indicated the formation of iron phosphate precipitation at the catalyst surface. The iron phosphate surface species may affect the amount of iron atoms taking part in the catalytic decomposition of H2O2 and formation of hydroxyl radicals, and inhibit the catalytic ability of Fe3O4 catalyst. Therefore, phosphate ions worked as stabilizer and inhibitor in a heterogeneous Fenton reaction at the same time, in effect leading to an increase in oxidation efficiency in this study. However, before use of phosphate as pH buffer or H2O2 stabilizer in a heterogeneous Fenton system, the possible inhibitory effect of phosphate on the actual removal of organic pollutants should be fully considered.
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