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Occurrences of perfluoroalkyl and polyfluoroalkyl substances (PFASs) in tree bark from four species were investigated. Species-dependent congener distribution patterns were firstly reported for perfluorocarboxylic acids (PFCAs) and perfluoroalkyl sulfonic acids (PFSAs). The majority of PFSAs and PFCAs in Chinese red pine bark were C5–C7 PFSAs and perfluorohexanoic acid (PFHxA, containing six carbon atoms, C6), whereas perfluorobutanesulfonic acid (PFBS, C4) and longer chain congeners (PFCAs: C ≥ 7; PFSAs: C ≥ 8) took a larger proportion in the fissured bark from Canadian poplar, Chinese scholartree and weeping willow. The species-dependent congener profiles depended on the structures and chemical compositions of tree bark, as well as the translocation of PFASs within plants. Different tree bark characteristics caused different retention abilities for particle-bound and gaseous PFASs. Particle-bound PFASs retained in the rougher structures of fissured bark led to preferential retention of long chain congeners (the major fraction in the particle phase), while lipid-rich Chinese red pine bark retained more gaseous PFASs (mainly short chain congeners). Besides, the abundance of short chain PFASs in red pine bark was consistent with the chain length-dependent translocation behaviors of PFASs in various plants, suggesting that translocation of PFASs within plants to tree bark may be invovled.

As one of the hard-templating methods, MgO-templating was employed to recycle cotton to produce activated carbon with magnesium acetate as MgO precursor. Results showed that cotton carbonized while magnesium acetate decomposed to nanoscale MgO particles based on thermogravimetric and X-ray diffraction analysis. Carbonized residuals of cotton were able to replicate the MgO morphology thus creating pores. The size of MgO varied with impregnation ratio, treatment temperature, and time. Overall, the optimum conditions were MgO/cotton impregnation ratio 0.25, temperature 800 °C, and treatment time 60 min. Cotton-based activated carbon thus produced manifested surface area and total pore volume of 1139 m2/g and 0.85 cm3/g respectively. Both micropores and mesopores were detected based on iodine, methylene blue adsorption values, and N2 adsorption-desorption studies.

For the most complex artificial chlorinated environmental contaminants, much less is known for medium-chain CPs than short-chain CPs. In this research, the spatial distributions of MCCPs and SCCPs in farmland soil and maize leaves near a CP production facility were found marginally influenced by seasonal winds. The levels of ∑MCCPs and ∑SCCPs were in the ranges of

Porous carbon was fabricated from cotton/polyester-based textile wastes as a carbon source coupled with oyster shells for tetracycline removal. The preparation conditions were optimized and detailed characterization was conducted to study the effects of oyster shells on cotton/polyester pyrolysis. The optimal pyrolysis temperature (900 °C), pyrolysis time (1 h) and mass ratio (OS/CPW of 1:1) were determined using the Box-Behnken experiment. The best porous carbon reached a surface area of 645.05 m2/g. Oyster shells acted as templates to produce cotton/polyester-based porous carbon and a possible pore-forming process was proposed. CaO was converted from CaCO3, which played the dominant role in developing the mesoporous structure. CO2 gas released from CaCO3 promoted the creation of micropore structure. In addition, the impurites of oyster shells acted as the dispersing agent inhibiting CaCO3 and CaO aggregation and growth. Fe2O3 and K2O from impurities reacted with the carbon skeleton to increase microporosity. Finally, the well-developed and uniform porous carbon was obtained. The first-pseudo order model and Langmuir isotherms were suitable. The maximum adsorption capacity of PC–OS–900 was 515.17 mg/g which competed with other waste-based adsorbents. The TET adsorption mechanism was related to pore distribution, hydrogen bonds, π-π EDA interactions and electrostatic interactions.

The cotton textile was an abundant energy resource while was otherwise treated as waste. In this work, surfactants were used as catalysts in the hydrothermal carbonization (HTC) to transform cotton textile waste (CTW) into clean solid fuel. Furthermore, the conversion mechanisms of hydrothermal products during surfactant-assisted HTC were preliminarily proposed. The results showed that Span 80 and sodium dodecylbenzenesulfonate facilitated the transformation of CTW into bio-oil, while Tween 80 was more conducive to the development of pseudo-lignin, which endowed hydrochars higher energy density and updated the fuel quality and combustion behavior. Therefore, the research presented an effective method to convert CTW to clean solid fuel through the HTC treatment combining with surfactants.

Short-chain and medium-chain chlorinated paraffins (SCCPs and MCCPs) are mixtures of complex chemical compounds with intensive usage. They are frequently detected in various environmental samples. However, the interaction between CPs and plants, especially the biotransformation behaviors of CPs within plants, is poorly understood. In this study, 1,2,5,6,9,10-hexachlorodecane (CP-4, a typical standard of individual SCCP congeners) and 52%-MCCP (a commercial mixture standard of MCCPs with 52% chlorine content by mass) were selected as representative chemicals to explore the metabolic behaviors of SCCPs and MCCPs using suspension rice cell culture exposure systems. Both 79.53% and 40.70% of CP-4 and 52%-MCCP were metabolized by suspension rice cells, respectively. A complementary suspected screening strategy based on the pair mass distances (PMD) analysis algorithm was used to study the metabolism of CPs mediated by the plant cells. Forty and 25 metabolic products for CP-4 and 52%-MCCP, respectively, were identified, including (multi-) hydroxylation, dechlorination, -HCl- elimination metabolites, (hydroxylation-) sulfation, and glycosylation conjugates. Here, we propose a comprehensive metabolic molecular network and provide insight on degradation pathways of SCCPs and MCCPs in plants for the first time, aiding in further understanding of the transformation behaviors of CPs.

In this work, the distribution of quaternary ammonium compounds (QACs) in two dated sediment cores, collected from the Pearl River Estuary (PRE) and Tokyo Bay (TB), were investigated to understand the historical input of QACs and their diagenetic behavior in urban estuarine environments. The vertical variation profiles of QAC concentrations showed that benzylalkyldimethyl ammonium compounds (BACs) and dialkyldimethyl ammonium compounds (DADMACs) were widely used during 1970s and 1980s both in China and Japan. The declining environmental concentrations of QACs suggested a compositional change of commodities and the effectiveness of emission control strategies. For the individual QAC homologues, BAC homologues decreased significantly over time, while DADMAC compositions remained relatively stable. The differences in concentration and composition profiles of BACs and DADMACs in the sediment cores provided useful information on the patterns of use of QACs in China and Japan, as well as their diagenetic behaviors in the sediments.

Textile waste jute was activated by H3PO4 and ZnCl2 for reuse as activated carbon. Thermal degradation behavior of jute, impregnated jute and activating agents via thermogravimetric analysis were conducted first. Yield and iodine adsorption number were employed to determine the optimal activation conditions. As a result, activation by H3PO4 was best conducted at 700 °C for 90 min with an impregnation ration of 1.0 while conditions for ZnCl2 were 500 °C, 60 min and impregnation ratio of 1.0. That is, the best activation conditions varied with activating agents. So were the properties of resultant jute-based activated carbons. H3PO4 activation produced an activated carbon that was mostly mesoporous while that by ZnCl2 was more even in micropore and mesopore volumes as proven by pore volume distribution analysis. In addition, both carbons were abundant in surface functional groups which could be beneficial for adsorption of pollutants. Overall, jute could be effectively recycled to produce activated carbon that boasted excellent surface chemistry and textual properties.

Activation-pyrolysis of textile wastes was considered a sustainable technique to fabricate activated carbon. Highly mesoporous activated carbon was prepared from waste polyester textiles by employing MgCl2 as the activation and template agents. The influences of different preparation conditions on textual property and crystalline structure of carbon were identified by N2 adsorption-desorption isotherms and X-ray diffraction. The optimum pyrolysis temperature, time and mixing ratio for MgCl2/waste polyester textiles are 900 °C, 1.5 h and 5:5 with the carbon thus obtained manifested a surface area of 1307 m2/g, total pore volume of 3.56 cm3/g of which 98% is mesopore. The effect of MgCl2 on the full-cycle pyrolysis pathway of waste polyester textiles was systematically investigated by various characterization methods to explore the pore-forming mechanism of activated carbon. The results demonstrated that MgCl2 was capable of catalyzing the dehydrogenation, decarboxylic and cross-linking reaction of waste polyester textiles and inhibited the formation of tars during pyrolysis process, indicating that the addition of MgCl2 was conducive to the formation of carbonaceous materials and open pores. Meanwhile, acted as the template, MgO particles derived from the decomposition of MgCl2 could develop massive homogeneous mesopores in the carbon matrix.

Two-step physical activation was used to prepare activated carbon from textile waste jute. Raw material was first carbonized under nitrogen and then activated by CO2. Based on yield and pore structure, the optimal carbonization temperature and time were 500 °C and 60 min, respectively. Carbonized sample was next activated. The development of porosity and surface chemistry was highly dependent on activation temperature and time. Activated carbon produced at 800 °C was predominantly microporous while that produced at 900 °C was more mesoporous and macroporous. The shift from microporosity to mesoporosity could be used to produce either microporous or mesoporous carbon just by changing the activation temperature. Activation also changed the surface chemistry and created a more carbonaceous structure. The jute-based activated carbon was mostly powdered in form, slightly acidic and effective in adsorbing both heavy metals and organics.

Pyrolysis activation of waste polyester textiles (WPT) was regarded as a sustainable technique to synthesize multi-pore activated carbons. MgO-template method of using MgCl 2 as the template precursor was employed, which possessed the advantages of ideal pore-forming effect and efficient preparation process. The response surface methodology coupled with Box-Behnken design (BBD) was conducted to study the interaction between different variables and optimized preparation conditions of waste polyester textiles based activated carbons. Derived from BBD design results, carbonization temperature was the most significant individual factor. And the maximum specific surface area of 1364 m 2 /g, which presented a good agreement with the predicted response values(1315 m 2 /g), was obtained at mixing ratio in MgCl 2 /WPT, carbonization temperature and time of 5:1, 900 °C and 90 min, respectively. Furthermore, the physicochemical properties of the sample prepared under optimal conditions were carried on utilizing nitrogen adsorption/desorption isotherms, EA, XRD, SEM and FTIR. In addition, the pore-forming mechanism was mainly attributed to the tendency of carbon layer coating on MgO to form pore walls after elimination of MgO and the strong dehydration effect of MgCl 2 on WPT.

Cotton textile waste-based magnetic activated carbon was prepared via simultaneous activation-pyrolysis using FeCl3 as a novel activating agent. The response surface methodology based on the Box–Behnken design method was applied to optimize the preparation parameters and predict the specific surface area of the samples. The optimal activated carbon was obtained at a mass ratio of FeCl3/CTW, activation time and activation temperature of 1.62 : 1, 1 h and 700 °C, respectively. The experimental maximum yield and iodine adsorptive value (32.66% and 714.55 mg g−1) of the resultant carbon were close to that of the predicated response values (34.85% and 783.75 mg g−1), respectively. SEM, N2 adsorption–desorption isotherms, XRD, PPMS, FTIR and pHpzc measurements were conducted to analyze the physicochemical characteristics of the optimal sample. The results showed that the carbon matrix had a high specific surface area of 837.39 m2 g−1 with abundant micropores and acidic surface functional groups, and the saturation magnetization (Ms) was 5.2 emu g−1 due to the formation of Fe3O4. The maximum adsorption of Cr(VI) by the carbon reached 212.77 mg g−1. Furthermore, the addition of FeCl3 lowered the pyrolytic carbonization temperature and inhibited the generation of volatiles in the activation-pyrolysis process. Meanwhile, the formation of Fe2O3 and Fe3O4 derived from FeCl3 was beneficial for the development of vast micropores.

The Kuroshio intrusion through the Luzon Strait into the northern South China Sea (SCS) is an important contributor to the heat and salt budgets of the SCS and is usually the strongest in winter. The extent of the intrusion in summer and the residence time of the very surface layer (0–5 m) in the northern SCS slope and basin areas, however, are seldom quantitatively evaluated. In this study we investigated surface distributions of radium isotopes (226Ra and 228Ra) across the Luzon Strait into the northern SCS in late spring to mid-summer to reveal the fraction of the Kuroshio water and the transport path of the Kuroshio intrusion in the northern SCS. The activity of 228Ra ranged from 0.67 to 23.5 dpm 100 L-1, with the maximum occurring at the lowest salinity of 28.8 on the northern SCS shelf and the minimum appearing east of the Luzon Strait characteristic of the more saline Ra-depleted Kuroshio water. The activity of 226Ra showed a similar pattern in a smaller range of 4.63–9.64 dpm 100 L-1. Distributions of 226Ra and 228Ra, combined with the distribution of salinity, demonstrate that three water masses contribute to the surface seawater in the northern SCS, the Kuroshio surface water, the plume water, and the island-influenced surface water. We quantified the fraction of the Kuroshio water in the northern SCS, considering the conservation of 226Ra and salinity, to be in the range of 4 ± 7%–51 ± 4% with an average of 23 ± 11%. The fraction decreased southward and westward from the northwest off the Luzon Strait. The intrusion of the Kuroshio reached as far west as 115° E and as far south as 14° N. The residence time of the very surface water in the northern SCS slope and basin areas was estimated using 228Ra as a timer to be 0.22 ± 0.59–9.98 ± 0.54 years with an average of 2.92 ± 2.20 years.

Activated carbons with high specific surface areas were produced, utilizing waste polyester textiles as carbon precursor by magnesium oxide (MgO) template method. Magnesium chloride (MgCl2), magnesium citrate (MgCi), and MgO were employed as MgO precursors to prepare activated carbons (AC-MgCl2, AC-MgCi, and AC-MgO). Thermogravimetry-differential scanning calorimetry was conducted to investigate the pore-forming mechanism, and N2 adsorption/desorption isotherms, XRD, SEM-EDS, TEM, FTIR and pHpzc were achieved to analyze physicochemical characteristics of the samples. The specific surface areas of AC-MgCl2 (1173 m2/g) and AC-MgCi (1336 m2/g) were much higher than that of AC-MgO (450 m2/g), and the pores sizes of which were micro-mesoporous, mesoporous, and macropores, respectively, due to the formation of MgO crystal with different sizes. All activated carbons had abundant acidic oxygen groups. In addition, batch adsorption experiments were carried out to investigate the adsorptive characteristics of the prepared activated carbons toward Cr(VI). The adsorption kinetics fitted well with the pseudo-second order, and the adsorptive capacity of AC-MgCl2 (42.55 mg/g) was higher than those of AC-MgCi (40.93 mg/g) and AC-MgO (35.87 mg/g).

To examine the impacts of urbanization and industrialization on the coastal environment, and assess the effectiveness of control measures on the contamination by chlorinated paraffins (CPs) in East Asia, surface and core sediments were sampled from the urbanized coastal zones in China and Japan (i.e., Pearl River Delta (PRD), Hong Kong waters and Tokyo Bay) and analyzed for short-chain (SCCPs) and medium-chain CPs (MCCPs). Much higher concentrations of CPs were found in the industrialized PRD than in adjacent Hong Kong waters. Significant correlation between CP concentration and population density in the coastal district of Hong Kong was observed (r2 = 0.72 for SCCPs and 0.55 for MCCPs, p < 0.05), highlighting the effect of urbanization. By contrast, a relatively lower pollution level of CPs was detected in Tokyo Bay. More long-chain groups within SCCPs in the PRD than in Hong Kong waters and Tokyo Bay implied the effect of industrialization. Comparison of temporal trends between Hong Kong outer harbor with Tokyo Bay shows the striking difference in historical deposition of CPs under different regulatory situations in China and Japan. For the first time, the declining CP concentrations in Tokyo Bay, Japan, attest to the effectiveness of emissions controls.

The implications of climate change during the second half of the 20th century have been reported throughout the world. Although marginal seas are sensitive to climate change and anthropogenic impacts, relatively little attention has been given to the South East Asian marginal seas. Thus, to bridge this gap in knowledge, a sediment core was collected from the coastal areas of the Leizhou Peninsula in the South China Sea (SCS) to study the inter-decadal climate change and its consequences using diatom species composition as a proxy record. Diatom absolute abundance varied from 2300 to 68000 and averaged 16000 valves per gram of dry weight (v/gdw). The fractional dissolution index (Fi) was usually below 0.5, which indicates low to moderate preservation of diatom valves at coastal area of the SCS. At the inter-decadal time scale, total diatom abundance was high for the period after 1972, which coincided with 1) increased percentage of planktonic diatom abundance and Fi; 2) emergence and dominance of high productivity indicative cosmopolitan species such as Thalassionema nitzschioides and Paralia sulcata (their relative abundance increased from 7% for the period before and after 1972, respectively); 3) decreased relative abundance of the small-sized eutrophication indicative species, Cyclotella striata, from 70% to 40%. This study reveals that variations in the abundance of diatoms preserved in the sediment was a function of both production and dissolution/preservation of diatom valves, which in turn was intimately connected to the prevailing environmental/climatic conditions. In conclusion, these data reveal the existence of substantial changes in the coastal SCS in response to the 1970s climate shift that was recorded in different parts of the world.

A novel GAC-Fe-Cu ternary micro-electrolysis system was synthesized for the removal of p-chloronitrobenzene (p-CNB) under oxic conditions. p-CNB could be efficiently removed by GAC-Fe-Cu at a wide initial pH range of 1.0–9.0. In particular, the p-CNB removal efficiency of 96.96 % was obtained at initial pH of 7.2, and the degradation (44.96 %) was the major removal pathway. Additionally, reduction and oxidation simultaneously contributed to the degradation of p-CNB. The results indicated that OH was the prime reactive species under acidic conditions while O2− dominated the degradation of p-CNB under neutral conditions. Reduction reaction was remarkably enhanced in the presence of dissolved oxygen and the iron corrosion could be accelerated by in-situ generated H2O2. Furthermore, XPS analysis of GAC-Fe-Cu revealed the surface-mediated electron transfer and oxidant generation process. The excellent degradation efficiency of p-CNB at initial pH of 7.2 was attributed to the enhanced electron selectivity of GAC-Fe-Cu as well as the high selectivity of near-surface generated O2− toward p-CNB and its intermediate products.

Char-based adsorbents (char-FeCl3, char-FeCl2, and char-FeCit) derived from cotton textile waste (CTW) were synthesized by one-step low-temperature pyrolysis approach with different iron salts. The properties of the samples were conducted by BET, SEM, EDS, XRD, XPS, TEM, and FTIR. The results suggested that the surface areas of char-FeCl3 and char-FeCl2 were higher than those of char-FeCit. The presence of Fe2O3 as well as pyrolysis gas (HCl (g) and H2O (g)) could catalyze the formation of porosity. Meanwhile, FeCl3 showed the strongest catalysis effect to decompose cellulose to produce char. The pyrolysis process analysis was investigated by means of thermogravimetry-DSC. FeCl3 and FeCl2 could accelerate the breakage of cellulose structure whereas FeC6H5O7 was not beneficial to form char at low temperature as the incomplete decomposition of citrate. The adsorption property of Cr(VI) for the chars was evaluated. Adsorption processes were fitted well with the Freundlich model, and char-FeCl3 presented the best adsorptive capacity (70.39 mg/g). Thus, this low-temperature pyrolysis method was economical and technologically simplified as well as efficient adsorption capacity of Cr(VI) removal.

Short chain chlorinated paraffins (SCCPs) are a group of complex emerging persistent organic pollutants. In this study, the uptake, translocation, and transformation of four constitutionally defined SCCP isomers were studied using whole pumpkin (Cucurbita maxima × C. moschata) and soybean (Glycine max L. Merrill) seedlings via hydroponic exposure. Results showed that the daughter SCCPs were C(10)Cl(5–8) and C(11–13)Cl(5–6). The metabolic transformation of all tested isomers included dechlorination and chlorine rearrangement. In addition, carbon chain decomposition products were found for isomers with trichlorinated carbon atoms (CCl(3)-groups) in both pumpkin and soybean seedlings. This study provides the first evidence of carbon chain decomposition of SCCPs in whole plants, and it suggests new metabolism pathways of SCCPs in the environment. The influence of carbon chain length and degree of chlorination of SCCPs on their fate and behavior within different plant species were also investigated. Bioaccumulation of SCCPs in pumpkin and soybean increased with increasing carbon chain length and degree of chlorination. In comparison, soybean translocated and degraded parent SCCPs faster and to a greater extent than pumpkin, but pumpkin accumulated parent SCCPs to a greater extent than soybean. After 10 days exposure, less than 4% of the initial mass of exposed chemicals remained in solution of exposure groups. The parent chemicals accumulated in roots ranging from 23.6% to 59.9% for pumpkin and 1.98% to 54.5% for soybean and in stems ranging from 0.7% to 3.81% for pumpkin and 0.50% to 2.54% for soybean. These results give new perspectives on the transport, transformation, and fate of SCCPs in the environment.

The degradation of organic contaminants in actual textile wastewater was carried out by iron carbon (Fe-C) micro-electrolysis. Different Fe-C micro-electrolysis systems (SIPA and SISA) were established by using scrap iron particle (SIP) and scrap iron shaving (SIS) as anode materials. The optimal condition of both systems was obtained at the initial pH of 3.0, dosage of 30 g/L and Fe/C mass ratio of 1:1. Commercial spherical Fe-C micro-electrolysis material (SFC) was used for comparison under the same condition. The results indicated that total organic carbon (TOC) and chroma removal efficiencies of SIPA and SISA were superior to that of SFC. Total iron concentration in solution and XRD analysis of electrode materials revealed that the former showed relatively high iron corrosion intensity and the physicochemical properties of scrap iron indeed affected the treatment capability. The UV-vis and 3DEEM analysis suggested that the pollutants degradation was mainly attributed to the combination of reduction and oxidation. Furthermore, the potential degradation pathways of actual textile wastewater were illustrated through the GC-MS analysis. Massive dyes, aliphatic acids, and textile auxiliaries were effectively degraded, and the SIPA and SISA exhibited higher performance on the degradation of benzene ring and dechlorination than that by SFC. In addition, SIPA and SISA exhibited high stability and excellent reusability at low cost. Graphical abstract.

Polyhalogenated carbazoles (PHCs) have been frequently detected in various environments and have gained increasing attention due to their dioxin-like toxicity. In this study, 28 surface sediments and three sediment cores were collected from the northern South China Sea (SCS) to investigate the spatial and temporal distribution trends of PHCs. The total concentrations of PHCs in the surface sediments ranged from 0.25 ng/g to 3.10 ng/g, with a median concentration of 1.50 ng/g. The composition profiles of PHCs in the surface sediments were dominated by 3,6-dichlorocarbazole (36-CCZ), 3,6-dibromocarbazole (36-BCZ), and 1,3,6,8-tetrabromocarbazole (1368-BCZ). The total organic carbon (TOC) based concentrations of 36-CCZ, 1-bromo-3,6-dichlorocarbazole, 1,3,6,8-tetrachlorocarbazole, and 1368-BCZ showed significant positive correlation with water depth (r = 0.58-0.88, p values 0.01). On the contrary, the TOC based concentration of 2,3,6,7-tetrachlorocarbazole displayed a significant negative correlation with the water depth (r = -0.52, p 0.01). However, no significant correlation was observed for 3-chlorocarbazole, 36-BCZ, and 1,3,6-tribromocarbazole (p values 0.05). PHCs in sediment cores showed that congener profiles and concentrations of PHCs remained largely stable throughout the 1890s and 2010s. In addition, all the detected PHCs displayed a significant positive correlation with TOC content of the sediments. These unique spatial and temporal distribution patterns suggest that both terrigenous and natural marine sources contributed the observed PHCs in sediments of the northern SCS.

In this study, the reduction of iron-carbon internal electrolysis was reinforced by persulfate for p-nitrophenol removal. The effects of persulfate dosage, initial pH and iron-carbon mass ratio were comprehensively studied in batch experiments. In the system of iron-carbon internal electrolysis coupled with persulfate, the iron-carbon internal electrolysis and persulfate had a significant mutual influence, exhibiting a wide range of pH in the treatment process. Moreover, the coupled system also showed the remarkable removal and degradation efficiency of p-nitrophenol according to the contrast experiments. The satisfactory results should be attributed to the potential reduction of iron-carbon internal electrolysis, which was stimulated by persulfate to transform the nitro group to the amine group, accompanying the subsequent oxidation. Furthermore, persulfate possessed the ability that the dynamically destructive effect on external and internal of Fe0 and the scavenging action on activated carbon, effectively strengthening the potential energy for release and transfer of reductive substances. Both HO• and SO4•- as the main free radicals were formed to mineralize the intermediates in the coupled system. These findings indicate that the system of iron-carbon internal electrolysis coupled with persulfate can be a promising strategy for the treatment of the toxic and refractory wastewater.

This study examines temporal variations of 234Th-based particle export based on time-series observations conducted from 2004 to 2014 at the South-East Asian Time-series Study (SEATS) site in the basin area of the Northern South China Sea. It shows significant variability in particle export at both seasonal and interannual time scales. A significant feature of our data as observed by prior studies is that particle export was high during the NE monsoon in winter, but low during the inter-monsoon and SW monsoon. Particle flux increased with increasing mixed layer depth (MLD), primarily in winter due to the presence of a strong NE monsoon, in addition to influence by mesoscale features quantified by eddy kinetic energy values. Particle export was generally elevated when phytoplankton biomass was abundant, as shown by the significant correlation between particle fluxes and concentrations of chlorophyll (Chl) a and/or particulate organic carbon (POC) between 0 and 100 m. This is also supported by the negative correlation between 234Th residence time and Chl a concentration, suggesting that increased phytoplankton biomass accelerated downward particle sinking. The correlation disappeared however at Chl a values

FeCl3 is a valuable iron salt used in the synthesis of magnetic waste cotton woven-based activated carbon. Although it has received extensive research attention, more information is required regarding its interactions with the carbon matrix. This systematic study describes the potential reactions of FeCl3 and waste cotton woven. First, the textural properties of waste cotton woven-based activated carbon synthesized under various conditions were investigated via element analysis, N2 sorption/desorption isotherms, and scanning electron microscopy. Then, the possible reaction mechanisms were deduced through various characterization methods. The results demonstrate that FeCl3 can lower the initial decomposition temperature of WCW to 135 °C and catalyze decarboxylation and decarbonylation at 100–330 °C to elevate the formation of microporous structures. Moreover, FeCl3 can also form Lewis acid sites at 330–700 °C and promote the cross-linking reaction to develop intricate microporous structures and carbonaceous materials with the synergistic effect of Fe3+ and Cl−. FeCl3 could be used as a template-like agent to form mesoporous structures. Meanwhile, it can also act as a magnetizer that Fe3O4 derived from the decomposition of FeCl3 would insert into the carbon matrix and combine with C–Cl to tailor the magnetic controllable activated carbon. Finally, we confirmed that extending the activation time could convert the structure of waste cotton woven-based activated carbon and increase the number of active sites, thereby further improving the catalytic properties of FeCl3 in pore formation.

Short chain chlorinated paraffins (SCCPs) are widely distributed persistent organic pollutants (POPs). Airborne chlorodecanes were hypothesized to be transformed by reactive phytogenic volatile organic compounds (PVOCs) in our previous work. To test this hypothesis, PVOCs of pumpkin (Cucurbita maxima × C. moschata) were collected and reacted with 1,1,1,3,8,10,10,10-octachlorodecane in the air phase of a sealed glass bottle under illumination for 10 days (reaction system I, simulating atmospheric reaction conditions with PVOCs). The reaction control group (reaction system II) was set at the same conditions but only had chlorodecane (without PVOCs) inside the bottle. Transformation of SCCPs in the air phase of reaction control group was unexpectedly found. Results showed that 1,1,1,3,8,10,10,10-octachlorode cane was transformed to a great extent to C(10)Cl(5–8), C(9)Cl(6–8), and C(8)Cl(7–8) in the air phase after 10-d illumination in both with and without the presence of PVOCs, which is explained by carbon chain decomposition, dechlorination and chlorine rearrangement products of the parent SCCP. Those transformation processes were increased to some extent by the PVOCs from pumpkin seedlings. This study provides the first experimental data on atmospheric transformation of SCCPs and also the first evidence that plant emissions (PVOCs) can increase the transformation of SCCPs in air under light and experimental conditions. It provides new insight into the potential transformation and fate of CPs in the environment.

Wheat flour is a necessity in our daily life. Wheat with impurities and pesticide residues will seriously affect the quality of wheat flour, and thereby wheat cleaning before milling is essential for the whiteness, purity, ash, pesticide residues, and other important indicators of flour. Wheat washing could refine wheat and remove stones with the dissolution and flushing of water, and meanwhile there are some shortcomings about the current wheat washing: fresh water consumption and pollution to the environment. For conserving fresh water and the environment, a novel water-saving cleaning technology based on rough–fine-washing separation has been proposed and investigated. In this, there are no chemical additives added in cleaning and no secondary pollution to the grain. And this can also bring us more safe food and reduced the pollution to the environment. In this paper, the principle of rough–fine-washing separation is first shown. Next, an experimental approach based on rough–fine-washing separation is developed. With the help of water-cycling system, the effective reuse for water is achieved. In order to verify the washing effect and the water-saving effect, the comparative experiments were done. The results show that the measurement values about cleaning effect are not reduced when the water consumption is only 1/3 of the traditional wheat washing. As the same time, the pollution to the environment is reduced radically with smaller water consumption, and the production cost of enterprises is significantly reduced with the decrease of water consumption.

Activated carbon-supported nano zero valent iron was synthesized through a carbonthermal reduction process. Specifically, iron-impregnated activated carbon was thermally treated under N2 atmosphere at temperatures ranging from 350 to 1,150°C. Major properties of the synthesized materials were obtained through analysis of iron content, BET surface area, and pore size distribution. TEM images, X-ray diffraction (XRD), and Fourier transform infrared patterns were also obtained for characterization. Results show that zero valent iron was reduced from iron oxide and those nanoparticles were highly dispersed based on TEM images while XRD patterns indicate a progressive reduction of iron oxide to form elemental iron. Treatment temperature greatly impacted the characteristics of the carbonthermal products. The size of the particles, content of elemental iron, surface functional groups, and pore structure all changed with the change in treatment temperature. Synthesized materials were tested for their reac...

A new hybrid material was prepared by loading the nanoscale iron oxide particles within the pores of granular activated carbon (GAC-NSIO) and used as adsorbent to remove Cd(II) in aqueous phase. The new material is characterized by the pHpzc, TEM, XRD, BET, and XPS analytical techniques to deduce the potential adsorptive mechanism, and further it along with GAC were assessed in the removal of Cd(II) from aqueous solution for various physico-chemical factors iron-loaded content, pH, humic acid, isotherm, kinetics, and thermodynamics, under the batch reactor studies and rapid small-scale column tests also appended dealing with the breakthrough volume. Characterization of adsorbent indicated that the amorphous nanoscale iron oxides were successfully immobilized on GAC. Adsorption mechanism mainly included surface complexation, Donnan membrane effect, and electrostatic attraction. The optimum iron-loaded content of GAC-NSIO was 17%. The adsorption process was more favorable at high pH, and iron oxide ...

Nanozero-valent iron/activated carbon (nZVI/AC) composite is investigated as a possible stabilization agent for heavy metals in river sediment. Effects of stabilization were tested by leaching tests such as synthetic precipitation leaching procedure (SPLP), atoxicity characteristic leaching procedure (TCLP), and a horizontal method that simulates various environmental conditions. In addition, changes in heavy metal forms before and after the addition of nZVI/AC were studied via sequential extraction method. Heavy metals such as Cu, Cd, and Pb were effectively stabilized by nZVI/AC. The stabilization could be attributed to the changes in bonding of heavy metal with sediment. The nZVI/AC in sediment increased the fraction of strongly bound heavy metals. Investigations on the impacts of nZVI/AC dosage, particle size, and time on stabilization and metal speciation showed that they all had significant effects. Generally, leaching dropped as dosage increased and a high dosage led to more metals in stron...

Intercomparision of 234 Th measurements in both water and particulate samples was carried out between 15 laboratories worldwide, as a part of GEOTRACES inter-calibration program. Particulate samples from four dif ferent stations namely BATS (both shallow and deep) and shelf station (shallow) in Atlantic and SAFE (both shallow and deep) and Santa Barbara station (shallow) in Pacific were used in the effort. Particulate intercali bration results indicate good agreement between all the participating labs with data from all labs falling with in the 95% confidence interval around the mean for most instances. Filter type experiments indicate no signif icant differences in 234 Th activities between filter types and pore sizes (0.2‐0.8 µm). The only exception are the

This study focused on comparing the occurrences and environmental toxic risks for diverse priority and emerging contaminants (>100 chemicals) in the sediments from the Pearl River Estuary (PRE, China). The most predominant compounds were cationic surfactants, organophosphate flame retardants (e.g., triisobutylphosphate), and polycyclic aromatic hydrocarbons (PAHs), accounting for >75% of the total mass inventory (∼330 metric tons). Wastewater discharges seem to be one of the main sources of pollution in the area, as the highest concentrations (>1000ngg-1 for some chemicals) were reported in the upper part of the PRE (near Guangzhou city) and Macau. Highest levels of ultraviolet (UV) filters, however, were observed in recreational areas, revealing the importance of direct sources (e.g., outdoor activities). An environmental risk assessment showed that PAHs and dichlorodiphenyl dichloroethylene had the highest hazard quotient (HQ) values (up to 233). Nonylphenol, a metabolite from nonionic surfactant, and two UV filters (2-ethyl-hexyl-4-trimethoxycinnamate and 4-methylbenzylidene camphor) also posed a significant threat to benthic species (HQ>1). Further research through the realization of monitoring campaigns and toxicity tests is encouraged, as the exposure of the resident aquatic organisms and human population to these and other emerging chemicals is expected to increase over the years.

Nano-zero-valent iron/activated carbon (nZVI/AC) composite was evaluated for its effectiveness in the stabilization of Cu, Pb, Cd, and Cr in dredged river sediment. Synthetic precipitation leaching procedure (SPLP) and toxicity characteristic leaching procedure (TCLP) were adopted to compare the effects of nZVI/AC dosage, particle size, time duration, and temperature on heavy metal leachability. The results show that leachability dropped considerably with the addition of nZVI/AC and powdered particles in the size of 0.075-0.18 mm was more effective in stabilization than granular ones. Stabilization effect was stable in long-term and robust against changes in temperature. Tessier sequential extraction revealed that heavy metals were associated with solid particle, inorganic or organic matters in sediment. The addition of nZVI/AC was able to convert relatively weakly bound heavy metals into more strongly bound species and thus reduce the bioavailability and toxicity. Also, the standard potential of heavy metals may decide the mechanism of stabilization process.

The separation process of eddy current separator is effected by the structure parameters of magnetic roller, the working parameters of the separator and some parameters of the scrap metal, such as the material, the shape, the size and so on. This is a complex process of electric field and magnetic field coupling. During this process, the sorting function of separator is powered by the existence of the eddy current power in waste particles, and the separation effect is directly determined by the flying distance of the scrap metal in the separation process. This paper armed for studying the eddy current power and the flying distance of the waste particles in separation to realize the simulation of the separation process. The eddy current force was obtained by the finite element analysis of the magnetic roller based on COMSOL, and the flying distance was got by the joint simulation of COMSOL and MATLAB.