Effective removal of microplastics by filamentous algae and its magnetic biochar: Performance and mechanism.

In recent years, filamentous algae blooms and microplastics (MPs) pollution have become two major ecological and environmental problems in urban water systems. In order to solve these two problems at the same time, this study explored the loading capacity of MPs on fresh filamentous algae, and successfully synthesized magnetic filamentous algae biochar loading with Fe3O4 by hydrothermal method, with the purpose of removing MPs from water. The magnetic filamentous algal biochar was characterized by scanning electron microscopy (SEM), Fourier transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and so on. Experiments on adsorption kinetics, adsorption isotherms and optimum pH were carried out to explore the adsorption mechanism of MPs on magnetic filamentous algal biochar. The adsorption kinetics and adsorption isotherm models were evaluated, and the selection criterion for the appropriate model was determined by using the residual sum of squares (RSS) and Bayesian information criterion (BIC). Microscope images revealed that fresh filamentous algae could interact with MPs in the form of entanglement, adhesion and encapsulation. The average load of MPs in filamentous algae samples was 14.1 ± 5 items/g dry weight. The theoretical maximum adsorption capacities of polystyrene MPs (PS-MPs) by raw biochar (A500) and magnetic biochar with Fe3O4 (M2A500) were 176.99 mg/g and 215.58 mg/g, respectively. The adsorbent materials gave better reusability because they could be reused up to five times. Overall, these findings have provided new insights into the use of filamentous algae for in situ remediation of fluvial MPs pollution, as well as feasible strategies for the recycling of algal waste.

Characterization of PCDD/Fs and heavy metal distribution from municipal solid waste incinerator fly ash sintering process.

A recycling and disposal technology for municipal solid waste incinerator (MSWI) fly ash using high temperature sintering process was evaluated in an industrial scale facility with daily disposal capacity of 100 t/d. The emission, mass balance and distribution characteristics of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) as well as heavy metals (HMs) were assessed during two test runs. The PCDD/Fs emission from stack varied in range of 0.019 to 0.025 ng I-TEQ /Nm3, below international standards. The PCDD/Fs in the sintered product was reduced to 0.002-0.008 µg I-TEQ/kg from 2.593 to 2.704 µg I- TEQ/kg of the original MSWI fly ash (Mix-FA). However high concentration of 14.3 µg I-TEQ/kg were found in the secondary fly ash (Sec-FA). Therefore, a large share of PCDD/Fs just desorbed from the ash and the destruction efficiency (DRE) for PCDD/Fs was only 8.9%. The distribution characteristics of investigated HMs were primarily dependent on the evaporative properties. The results of HMs leaching test for the sintered product were considerably below the Chinese legal limits. The HMs leaching toxicity test for Sec-FA indicated which is a hazardous waste presented high risk to the environment. The use of the sintered product as construction material need further assessment on its long term HMs leaching behavior.

Mechanistic aspects of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) formation from chlorine bleaching of non-wood pulp.

Chlorine bleaching of non-wood pulp can produce and release polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) into environment. In this study, a series of chlorination experiments were conducted to explore the source, formation pathway and formation kinetics of Cl1-8DD/Fs during the chlorine bleaching of wheat straw pulp. The 13C isotope-labeling experiment verified that PCDD/Fs could not be formed from the chlorination of phenols in pulp. Above 80% of the observed PCDFs originated from the direct chlorination of dibenzofuran (DBF) in unbleached wheat straw pulp, while approximately 60% of the observed PCDDs came from the chlorination of nonextractable precursors in the pulp. The yield of total PCDFs was 2 orders of magnitude higher than that of total PCDDs. The kinetic study indicated that DBF was more easily chlorinated than dibenzo-p-dioxin (DBD) in the pulp solution. Pseudo-first-order reaction kinetic equations fitted the formation and degradation of PCDD/Fs well. The direct chlorination of DBD/F primarily preferred a selective pattern at the 2 position, followed by the 8, 7 and 3 positions. A higher content of DBF in unbleached pulp led to a higher yield of 2,3,7,8-Cl4DF. Finally, the practical implication for dioxin formation control was discussed.

Occurrence and characteristics of PCDD/Fs formed from Chlorobenzenes production in China.

China had a large production capacity of chlorobenzenes. An extensive investigation was conducted to understand the occurrence and characteristics of PCDD/Fs from four chlorobenzene production plants. The concentrations of PCDD/Fs in mono-CB production and in a new di-CB production routine were revealed. Concentrations of PCDD/Fs in residues, byproducts, products and wastewater varied between 8.4*103-4.0*106 ng TEQ/kg, 1.5-5.0*104 ng TEQ/kg, ND∼0.12 ng TEQ/kg and 6.0*104-9.1*104 pg TEQ/L, respectively. OCDF, 2,3,4,7,8-PeCDF, 1,2,3,4,7,8-HxCDF, and 2,3,7,8-TeCDF were the most abundant congeners of the 17 2,3,7,8-substituted PCDD/Fs. In most samples, PCDFs contributed more than 99% of the total TEQs of PCDD/Fs, in which 2,3,4,7,8-PeCDF was the dominating contributor. It is inferred PCDFs were mainly formed in the chlorination reactions. The emission factors were suggested and the amount of PCDD/Fs formed in CB production was estimated to be 450 g TEQ in 2012. Residue, byproduct and wastewater were potentially the main pathways of PCDD/Fs to the environmental releases.

Characterization of heavy metals and PCDD/Fs from water-washing pretreatment and a cement kiln co-processing municipal solid waste incinerator fly ash.

A disposal method for fly ash from a municipal solid waste incinerator (MSWI-FA) that involved a water washing pretreatment and co-processing in a cement kiln was tested. The mass flows of toxic heavy metals (HMs), including volatile HM (Hg), semi-volatile HMs (Pb, Cd, Tl, and As), and low-volatility HMs, and polychlorinated dibenzo-p-dioxin/polychlorinated dibenzofuran (PCDD/Fs) in the input, intermediate, and output materials were characterized. The flue gas Hg concentrations from tests 0, 1, and 2, fed with 0, 3.1, and 1.7 t/h of dried-washed FA (DWFA), were 28.60, 61.95, and 35.40 µg N m-3, respectively. Co-processing of DWFA did not significantly affect the metal concentration in clinker as most of the major input metals, with the exception of Cd, Pb, and Sb (which came from DWFA), were from raw materials and coal. Co-processing of DWFA did not influence on the release of PCDD/Fs; baseline and co-processing values ranged from 0.022 to 0.039 ng-TEQ/N m3, and from 0.01 to 0.031 ng-TEQ/N m3, respectively. The total destruction efficiency for PCDD/Fs in MSWI fly was 82.6%. This technology seems to be an environmentally sound option for the disposal of MSWI-FA.

[Level, composition and sources of medium-chain chlorinated paraffins in soils from Chongming Island].

In order to understand the contents, spatial distribution and sources of medium-chain chlorinated paraffins (MCCPs) in the soils from Chongming Island, the concentrations of MCCPs in 27 soil samples were analyzed by GC-ECNI-MS. The total concentrations of MCCP8 (sigma MCCPs) in all samples ranged from 2.56-96.3 ng x g(-1), with a median of 7.32 ng x g(-1). All soil samples were classified into two categories by cluster analysis. C14-MCCPs and C15-MCCPs, and Cl5-MCCPs and Cl6-MCCPs were the most predominant carbon and chlorine congener groups in most of the samples, accounting for 29.8% and 28.9%, and 29.9% and 23.3%, respectively. C14-MCCPs were the most predominant carbon congener groups in some samples, accounting for 68.5%, which was similar to that of CP-52. Atmospheric deposition and soil-air exchange were the major sources of MCCPs for soils in Chongming. Soils at a few sites were probably contaminated by sewage sludge from sewage treatment plants (STPs) or other unidentified source. No significant correlations were observed between MCCPs and TOC. The correlation analysis also showed significant correlation among the carbon congener groups of MCCPs, which suggested that MCCP congener groups might have been derived from similar sources. Compared to other studies at home and abraod, the MCCPs concentrations in the present study were at a lower level.

[Levels, distribution and possible sources of polychlorinated biphenyls in river sediments from an electronic waste recycling area].

The concentrations of 144 polychlorinated biphenyls (PCBs) in the river sediments from Luqiao were analyzed by GC-muECD. The objectives of this study were to understand the contents, spatial distribution and possible sources of PCBs. The Sigma PCBs concentrations detected in the river sediments were in the range of 1.66 to 5 930 ng x g(-1), with a mean of 763 ng x g(-1). Tri-CBs, tetra-CBs and penta-CBs were the primary PCB congeners in all samples, accounting for 2.63%-57.6%, 10.4%-54.6% and 7.82%-46.1%, respectively. Octa-CBs and deca-CBs were the minor PCB congeners in all samples, with the percentages of 0-8.57% and 0-11.0%, respectively. The hierarchical cluster analysis (HCA) showed that 22 samples were mainly polluted by Ar1248, 9 samples were polluted by Ar1254, and 6 samples were contaminated by Ar1016, Ar1232 and Ar1242. The PCBs concentrations found in the present study were at an upper-middle level compared with those in other studies in the world. The PCBs pollution in the present area had a high ecological risk.

[Characteristics of polychlorinated biphenyls in soils from an electronic waste recycling area].

The concentrations of 144 polychlorinated biphenyls (PCBs) in the soils from Luqiao were analyzed by GC-microECD. The objectives of this study were to understand the contents, spatial distribution and sources. The sigma PCBs concentrations in soils samples were in the range of 0.779 ng x g(-1) to 937 ng x g(-1), with a mean of 75.7 ng x g(-1), and the relatively high level of PCBs were mainly distributed in the south central area. Penta-CBs, hexa-CBs and tetra-CBs were the primary homologues in 38 samples, with the range of 13.0% - 61.1%, 4.59% - 48.8% and 10.1% - 31.5%, respectively. Di-CBs was the most predominant homologues in other samples, with the range of 47.1% - 75.2%. The hierarchical cluster analysis (HCA) showed that most of samples were mainly polluted by Ar1254, few samples were polluted by Ar1221. Significant correlations were observed between sigma PCBs and TOC, which suggested PCBs were affected by TOC in soils. The correlation analysis also showed significant correlation among the PCBs homologues (except di-CBs and nona-CBs), which suggested PCBs might have the similar sources. Compared to other studies from different countries and regions, the PCBs concentrations in the present study were at an upper-middle level.

[Level, distribution, and source identification of polychlorinated naphthalenes in surface agricultural soils from an electronic waste recycling area].

The concentration of 46 polychlorinated naphthalenes (PCNs) in the agricultural soils from Luqiao was analyzed by GC-NCI-MS. The objectives of this study were to investigate the contents, spatial distribution and sources of PCNs. The total concentrations of PCNs (sigma PCNs) in soil samples were in the range of 0.062 to 2.92 ng x g(-1), with a mean of 0.630 ng x g(-1). Tetra-CNs and penta-CNs were the predominant homologues in most of the samples, accounting for 18.4% - 88.8% and 8.40% - 53.1%, with average values of 46.7% and 30.7%, respectively, followed by tri-CNs, accounting for 0 - 47.3%, with a mean of 10.6%. Cluster analysis and combustion marker analysis showed that the sampling sites were mainly polluted by Halowax 1014 and Halowax 1013, also possibly polluted by PCBs mixtures and e-waste combustion process. Compared to other studies, the PCNs concentration in this study was at a medium level.

[Levels, distribution and possible sources of polybrominated diphenyl ethers in river sediments from an electronic waste recycling area].

The concentrations of 41 polybrominated diphenyl ethers (PBDEs) in the river sediments from Luqiao were analyzed by GC-NCI-MS. The objectives of this study were to understand the contents, spatial distribution and sources. The Sigma40 PBDEs (excluding BDE209) concentrations in sediments sampled were in the range of 0.177 to 161 ng x g(-1), with a mean of 22.5 ng x g(-1), and the concentrations of BDE209 were from 0.36 to 958 ng x g(-1), with a mean of 148 ng x g(-1). Deca-BDE was the most predominant in 9 PBDE homologues in most of samples, accounting for 38.4%-96.0%, with an average of 74.4% nona-BDEs and hepta-BDEs, accounting for 3.3%-25.8% and 0.01%-14.1%, respectively. Significant correlations were observed among all of PBDEs congeners, which suggested these PBDEs might have the similar sources. The homologue composition of PBDEs and hierarchical cluster analysis (HCA) showed that most of sampling sites were mainly polluted by deca-BDE formulation, and others polluted by deca-BDE and octa-BDE formulations. Compared to other studies from different countries and regions, the PBDEs concentrations in the present study were at a medium-to-low level. But it should be concerned that a few of sampling sites were highly contaminated by point sources.

[Residues of organochlorine pesticides in urban soil of Shanghai].

The 55 soil samples were collected from Shanghai urban areas in March 2007. The residues and distribution characteristics of organochlorine pesticides (OCPs) in the soil samples were investigated with gas chromatography. The results showed that HCHs, DDTs, and HCB were in the ranges of nd-38.58 microg x kg(-1), 1.81-79.61 microg x kg(-1) and 0.16-40.25 microg x kg(-1), respectively. The total OCPs concentrations in urban soil of Shanghai ranged from 3.12 microg x kg(-1) to 91.07 microg x kg(-1) with a mean of 22.33 microg x kg(-1), and the p,p'-DDE took over 60% of the total OCPs. The main contaminated areas were distributed in the park and greenbelts. The composition of OCPs indicated that OCPs in soil samples mainly came from historical application. Compared to the reference data, the pollution burden in soil of Shanghai was lower than those in other areas of China and in German, Argentina and Poland.

[Distribution, possible source and ecological risk assessment of polycyclic aromatic hydrocarbons in river sediments from a typical contaminated area].

The concentrations of 16 US EPA PAHs in 37 sediment samples collected from Luqiao were analyzed by isotope dilution gas chromatograph/mass spectrometer (GC/MS), and their distribution characters,sources and ecological risk were further investigated. Each of the 16 PAHs could be detected in all of the sediment samples, the total concentrations of the 16 PAHs in the sediments ranged from 59.3 microg/kg to 3 180 microg/kg,with a mean of 722 microg/kg. The pollution level of PAHs can be categorized as low to moderate when compared with other studies around the world. SigmaPAHs were significantly correlated with TOC (r = 0.699, p < 0.001), indicating that TOC was a key soil property affecting the level and fate of PAHs in sediments. The isomeric ratios and factor analysis revealed that PAHs in the Luqiao sediments were originated from mixed sources, and combustion source was dominant. Six sampling sites had the mean PAH ERL quotient > 1, indicating that some sediments in Luqiao may have potential ecological risk. The toxic benzo[a]pyrene equivalents (TEQ(BaP)) of the 16 PAHs ranged from 3.41 microg/kg to 485 microg/kg, 98.4% of which was contributed by 7 carcinogenic PAHs, indicating that 7 PAHs were the main influential factors to the ecological risk.

Characterization of mechanochemical treated fly ash from a medical waste incinerator.

The mechanochemical treatment of fly ash generated from a medical waste incinerator was subjected to grinding for 2 hr at 400 r/min in a planetary ball mill. The treated fly ash was characterized by a suite of analytical methods including High Resolution Gas Chromatograph/High Resolution Mass Spectrometer, Mastersizer 2000 Particle Size Analyzer, QUADRASORB SI Surface Area Analyzer, Scanning Electron Microscopy and X-ray diffraction. Results showed that abatement efficiency of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDDs/Fs) in terms of total concentration averagely amount to 76% which was relatively higher than that of I-TEQ concentration averagely amount to 56%; the most concentration of toxic congeners as well as isomers of PCDDs/Fs decreased after mechanochemical treatment. The treated fly ash was characterized by a more homogeneous distribution of concaves as well as the significant decreasing in overall particle size and great enlargement in surface area. The major crystallization phases or intensities were considerably changed by mechanochemical treatment, of which a new phase containing chlorine formed may be a possible factor suggesting chlorination reaction occurring on the crystalline surface.

Optimization of ultrasound-assisted extraction of anthocyanins in red raspberries and identification of anthocyanins in extract using high-performance liquid chromatography-mass spectrometry.

Anthocyanins (Acys) are naturally occurring compounds that impart color to fruit, vegetables and plants. The extraction of Acys from red raspberry (Rubus idaeus L. var. Heritage) by ultrasound-assisted process (UAP) was studied. A central composite rotate design (CCRD) was used to obtain the optimal conditions of ultrasound-assisted extraction (UAE), and the effects of operating conditions, such as the ratio of solvents to materials, ultrasonic power and extraction time, on the extraction yield of Acys were studied through response surface methodology (RSM). The optimized conditions of UAE were as follows: ratio of solvents to materials was 4:1 (ml/g), extraction time was 200s, and ultrasonic power was 400 W. Under these conditions 34.5 mg of Acys from 100g of fresh fruits (T(Acy), expressed as cyanidin-3-glucoside), approximately 78.13% of the total red pigments, could be obtained by UAE. The Acys compositions of extracts were identified by high-performance liquid chromatography-mass spectrometry (HPLC-MS), 12 kinds of Acys had been detected and eight kinds of Acys were characterized. Result indicated that cyanidin-3-sophoroside, cyanidin-3-(2(G)-glucosylrutinoside), cyanidin-3-sambubioside, cyanidin-3-rutinoside, cyanidin-3-xylosylrutinoside, cyanidin-3-(2(G)-glucosylrutinoside), and cyanidin-3-rutinoside were main components in extracts. In addition, in comparison with the conventional solvent extraction, UAE is more efficient and rapid to extract Acys from red raspberry, due to the strong disruption of fruit tissue structure under ultrasonic acoustic cavitation, which had been observed with the scanning electron microscopy (SEM). However, the Acys compositions in extracts by both methods were similar, which were investigated using HPLC profile.

Distribution of persistent organochlorine pesticides in tissue/organ of silver carp (Hypophthalmichthys molitrix) from Guanting Reservoir, China.

The concentration of organochlorine pesticides (OCPs) in tissues and organs of silver carp (Hypophthalmichthys molitrix) from Guanting Reservoir were investigated to evaluate the pollution potential and distribution of OCPs. A total of 16 OCPs were measured and the concentrations were in the range of 1.61-69.01 ng/g wet weight (ww) for total OCPs, 0.16-0.75 ng/g ww for. HCB, 0.75-26.80 ng/g ww for sigmaHCH (sum of alpha-, beta-, gamma- and delta-HCH) and 0.68-35.94 ng/g ww for sigmaDDT( sum of p, p'-DDE, p, p'-DDD, o, p'-DDT and p, p'-DDT). The mean concentrations of total OCPs, HCB, sigmaHCH, and sigmaDDT were 18.04, 0.96, 7.14 and 9.28 ng/g ww, respectively. Among the organochlorine pesticides, beta-HCH and p, p'-DDE were the most dominant compounds in tissue and organ with the average concentrations of 4.42 and 8.14 ng/g, respectively. The results obtained in this study show that the levels of 16 OCP residues found in silver carps are low and pose no threat to human health and wildlife fed upon them on the basis of existing related quality guidelines. However, recent input of lindane and DDT might still exist in the area investigated and further investigation should be carried on.