ORCID Profile
0000-0002-2147-5609
Current Organisation
University of South Australia
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Publisher: Shanghai Institute of Organic Chemistry
Date: 2015
DOI: 10.6023/A15070520
Publisher: Elsevier BV
Date: 10-2002
Publisher: Springer Science and Business Media LLC
Date: 12-02-2015
DOI: 10.1007/S10661-014-4202-Y
Abstract: From data collected monthly at 26 monitoring cross sections in the Wei River in the Shaanxi Region of China during the period 2008-2012, the temporal pollution characteristics of heavy metals (Hg, Cd, Cr(VI), Pb, and As) were analyzed based on a heavy metal pollution index (HPI). The monthly HPI values of the five heavy metals in the river fluctuated greatly in 2008 and then declined gradually with time. This general trend of reduction in HPI appears not to have a seasonal variation and most likely resulted from the continued improvement in heavy metal pollution control strategies implemented by local environmental agencies combined with a significant improvement in wastewater treatment capacities. Among the five heavy metals, Cd and Pb were below 0.1 and 3 μg L(-1), respectively, at all the s ling points in the studied areas in the year 2012. The detection rates of As, Hg, and Cr(VI) were in the order of Hg > Cr(VI) > As. Hg, Cr(VI), and As exceeded, in a month of the dry season in 2012, the standard limits for category III surface waters according to the China Environment Quality Standards for Surface Water (CEQSSW). Based on the assessment using the HPI method, the pollution status of these heavy metals in water of the Wei River in the Shaanxi Region was generally at an acceptable level, but exhibited distinctive characteristics between the main stream river and tributaries. Most of the tributaries were more seriously polluted than the main river. A health risk assessment was conducted based on the Human Health Risk Assessment (HHRA) method recommended by the United States Environmental Protection Agency (USEPA). Apart from As, the health risk for the five heavy metals in the region were at acceptable levels for drinking water sources (hazard quotient (HQ) < 1, carcinogenic risk (CR) ranged from 10(-4)-10(-6)) according to the Risk Assessment Guidance for Superfund (RAGS), USEPA. Arsenic was identified as the most important pollutant of concern among the five heavy metals both its values of the HQ and CR indicated potentially adverse health risks for the local population.
Publisher: Elsevier BV
Date: 06-2017
DOI: 10.1016/J.JCIS.2017.02.054
Abstract: Anatase TiO
Publisher: Elsevier BV
Date: 04-2015
DOI: 10.1016/J.CHROMA.2015.02.044
Abstract: Liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis coupled simply with water filtering before injection has proven to be a simple, economic and time-saving method for analyzing trace-level organic pollutants in aqueous environments. However, the linearity, precision and detection limits of such methods for late-eluting analytes were found to be much poorer than for early-eluting ones due to adsorption of the analytes in the operating system, such as s le vial, flow path and s le loop, creating problems in quantitative analysis. Addition of methanol (MeOH) into water s les as a modifier was shown to be effective in alleviating or even eliminating the negative effect on signal intensity for the late-eluting analytes and at the same time being able to reduce certain matrix effects for real water s les. Based on the maximum detection signal intensity obtained on desorption of the analytes with MeOH addition, the ratio of the detection signal intensity without addition of MeOH to the maximum intensity can be used to evaluate the effectiveness of methanol addition. Accordingly, the values of <50%, 50-80%, 80-120% could be used to indicate strong, medium and no effects, respectively. Based on this concept, an external matrix-matched calibration method with the addition of MeOH has been successfully established for analyzing fifteen pesticides with erse physico-chemical properties in surface and groundwater with good linearity (r(2): 0.9929-0.9996), precision (intra-day relative standard deviation (RSD): 1.4-10.7%, inter-day RSD: 1.5-9.4%), accuracy (76.9-126.7%) and low limits of detection (0.003-0.028μg/L).
Publisher: Elsevier BV
Date: 2003
Publisher: Shanghai Institute of Organic Chemistry
Date: 2019
DOI: 10.6023/A18090365
Publisher: American Chemical Society (ACS)
Date: 09-08-2018
DOI: 10.1021/ACS.LANGMUIR.8B02249
Abstract: Bubble-driven micromotors have attracted substantial interest due to their remarkable self-motile and cargo-delivering abilities in biomedical or environmental applications. Here, we developed a hollow micromotor that experiences fast self-propulsion underneath an air-liquid interface by periodic bubble growth and collapse. The collapsing of a single microbubble induces a ∼1 m·s
Publisher: MDPI AG
Date: 14-04-2023
DOI: 10.3390/MOLECULES28083478
Abstract: The application of fungicides (such as tebuconazole) can impose harmful impacts on the ecosystem and humans. In this study, a new calcium modified water hyacinth-based biochar (WHCBC) was prepared and its effectiveness for removing tebuconazole (TE) via adsorption from water was tested. The results showed that Ca was loaded chemically (CaC2O4) onto the surface of WHCBC. The adsorption capacity of the modified biochar increased by 2.5 times in comparison to that of the unmodified water hyacinth biochar. The enhanced adsorption was attributed to the improved chemical adsorption capacity of the biochar through calcium modification. The adsorption data were better fitted to the pseudo-second-order kinetics and the Langmuir isotherm model, indicating that the adsorption process was dominated by monolayer adsorption. It was found that liquid film diffusion was the main rate-limiting step in the adsorption process. The maximum adsorption capacity of WHCBC was 40.5 mg/g for TE. The results indicate that the absorption mechanisms involved surface complexation, hydrogen bonding, and π–π interactions. The inhibitory rate of Cu2+ and Ca2+ on the adsorption of TE by WHCBC were at 4.05–22.8%. In contrast, the presence of other coexisting cations (Cr6+, K+, Mg2+, Pb2+), as well as natural organic matter (humic acid), could promote the adsorption of TE by 4.45–20.9%. In addition, the regeneration rate of WHCBC was able to reach up to 83.3% after five regeneration cycles by desorption stirring with 0.2 mol/L HCl (t = 360 min). The results suggest that WHCBC has a potential in application for removing TE from water.
Publisher: Elsevier BV
Date: 07-2020
Publisher: American Chemical Society (ACS)
Date: 09-05-2013
DOI: 10.1021/JP4027578
Publisher: Elsevier BV
Date: 09-2012
DOI: 10.1016/S1001-0742(11)60953-4
Abstract: The effects of addition of calcium hydroxide on aluminum sulphate (or alum) coagulation for removal of natural organic matter (NOM) and its subsequent effect on the formation potentials of two major types of regulated disinfection byproducts (DBPs), haloacetic acids (HAAs) and trihalomethanes (THMs), have been examined. The results revealed several noteworthy phenomena. At the optimal coagulation pH (i.e. 6), the coagulation behavior of NOM water solutions versus alum dose, showed large variation and a consequent great change in the formation potentials of the DBPs at certain coagulant doses. However, with addition of a relatively small amount of Ca(OH)2, although the zeta potential of coagulated flocs remained almost the same, NOM removal became more consistent with alum dose. Importantly, also the detrimental effect of charge reversal on NOM removal at the low coagulant dose disappeared. This resulted in a steady decrease in the formation potentials of DBPs as a function of the coagulant dose. Moreover, the addition of Ca(OH)2 broadened the pH range of alum coagulation and promoted further reduction of the formation potentials of the DBPs. The enhancement effects of Ca(OH)2 assisted alum coagulation are especially pronounced at pH 7 and 8. Finally, synchronous fluorescence spectra showed that the reduction in DBPs formation potential by Ca(OH)2-assisted alum coagulation was connected to an enhanced removal of small hydrophobic and hydrophilic HA molecules. Ca(OH)2-assistance of alum coagulation appeared to increase substantially the removal of the hydrophilic HA fraction responsible for HAAs formation, prompting further reduction of HAA formation potentials.
Publisher: Elsevier BV
Date: 02-2014
DOI: 10.1016/S1001-0742(13)60437-4
Abstract: Insights from the adverse effect of humic acid (HA) on arsenate removal with hydrous ferric oxide (HFO) coprecipitation can further our understanding of the fate of As(V) in water treatment process. The motivation of our study is to explore the competitive adsorption mechanisms of humic acid and As(V) on HFO on the molecular scale. Multiple complementary techniques were used including macroscopic adsorption experiments, surface enhanced Raman scattering (SERS), extended X-ray absorption fine structure (EXAFS) spectroscopy, flow-cell attenuated total reflectance Fourier transform infrared (ATR-FTIR) measurement, and charge distribution multisite complexation (CD-MUSIC) modeling. The As(V) removal efficiency was reduced from over 95% to about 10% with the increasing HA concentration to 25 times of As(V) mass concentration. The SERS analysis excluded the HA-As(V) complex formation. The EXAFS results indicate that As(V) formed bidentate binuclear surface complexes in the presence of HA as evidenced by an As-Fe distance of 3.26-3.31 angstroms. The in situ ATR-FTIR measurements show that As(V) replaces surface hydroxyl groups and forms innersphere complex. High concentrations of HA may physically block the surface sites and inhibit the As(V) access. The adsorption of As(V) and HA decreased the point of zero charge of HFO from 7.8 to 5.8 and 6.3, respectively. The CD-MUSIC model described the zeta potential curves and adsorption edges of As(V) and HA reasonably well.
Publisher: Elsevier BV
Date: 05-2014
DOI: 10.1016/J.JHAZMAT.2014.03.030
Abstract: Insights from the molecular-level mechanism of sorption of organophosphate esters (OPEs) on carbon nanotubes (CNTs) can further our understanding of the fate and transport of OPEs in the environment. The motivation for our study was to explore the sorption process of OPEs on multi-walled CNTs (MWCNTs), single-walled CNTs (SWCNTs) and their oxidized counterparts (O-MWCNTs and O-SWCNTs), and its molecular mechanism over a wide concentration range. The sorption isotherm results revealed that the hydrophobicity of OPEs dominated their affinities on a given CNT and the π-π electron donor-acceptor (EDA) interaction also played an important role in the sorption of aromatic OPEs. This π-π EDA interaction, verified with Raman and FT-IR spectroscopy, could restrict the radial vibration of SWCNTs and affect the deformation vibration γ(CH) bands of OPE molecules. The OPE surface coverage on CNTs, estimated using the nonlinear Dubinin-Ashtakhov model, indicated that the oxygen-containing functional groups on CNTs could interact with water molecules by H-bonding, resulting in a decrease in effective sorption sites. In addition, FTIR analysis also confirmed the occurrence of Brønsted acid-base interactions between OPEs and surface OH groups of SWCNTs. Our results should provide mechanistic insights into the sorption mechanism of OPE contaminants on CNTs.
Publisher: MDPI AG
Date: 22-03-2023
DOI: 10.3390/MOLECULES28062868
Abstract: To remove typical herbicide diuron effectively, a novel sludge-derived modified biochar (SDMBC600) was prepared using sludge-derived biochar (SDBC600) as raw material and Fe-Zn as an activator and modifier in this study. The physico-chemical properties of SDMBC600 and the adsorption behavior of diuron on the SDMBC600 were studied systematically. The adsorption mechanisms as well as practical applications of SDMBC600 were also investigated and examined. The results showed that the SDMBC600 was chemically loaded with Fe-Zn and SDMBC600 had a larger specific surface area (204 m2/g) and pore volume (0.0985 cm3/g). The adsorption of diuron on SDMBC600 followed pseudo-second-order kinetics and the Langmuir isotherm model, with a maximum diuron adsorption capacity of 17.7 mg/g. The biochar could maintain a good adsorption performance (8.88–12.9 mg/g) under wide water quality conditions, in the pH of 2–10 and with the presence of humic acid and six typical metallic ions of 0–20 mg/L. The adsorption mechanisms of SDMBC600 for diuron were found to include surface complexation, π–π binding, hydrogen bonding, as well as pore filling. Additionally, the SDMBC600 was tested to be very stable with very low Fe and Zn leaching concentration ≤0.203 mg/L in the wide pH range. In addition, the SDMBC600 could maintain a high adsorption capacity (99.6%) after four times of regeneration and therefore, SDMBC600 could have a promising application for diuron removal in water treatment.
Publisher: American Chemical Society (ACS)
Date: 11-03-2013
DOI: 10.1021/JP3121935
Publisher: Elsevier BV
Date: 10-2007
Publisher: Elsevier BV
Date: 03-2015
Publisher: Elsevier BV
Date: 02-1996
Publisher: Royal Society of Chemistry (RSC)
Date: 2011
DOI: 10.1039/C0AY00507J
Publisher: American Chemical Society (ACS)
Date: 11-03-2003
DOI: 10.1021/JP021751L
Publisher: Elsevier BV
Date: 08-2017
Publisher: Elsevier BV
Date: 02-2003
Publisher: Elsevier BV
Date: 12-2005
Publisher: Royal Society of Chemistry (RSC)
Date: 2023
DOI: 10.1039/D2EW00376G
Abstract: An optimized electrocoagulation process was investigated for enhanced removal of dissolved organic matter for eco-friendly drinking water production from surface water sources. A model-based control system was developed for electro-coagulant dosing.
Publisher: Royal Society of Chemistry (RSC)
Date: 2007
DOI: 10.1039/B709624K
Abstract: The kinetics of adsorption of CO(2) molecules dissolved in aqueous solution onto a hydrophobised silica surface were investigated using a quartz crystal microbalance (QCM). The results of this investigation were compared with those obtained earlier from tapping mode atomic force microscopy (TMAFM) under the same experimental conditions (J. Yang, J. Duan, D. Fornasiero, J. Ralston, J. Phys. Chem. B., 2003, 107(25), 6139-6147 ref. 1). The QCM results represent the early stage of CO(2) gas adsorption (<20 min), before CO(2) gas bubbles adsorbed on the surface can be directly observed by TMAFM. The QCM results confirmed our observation from TMAFM imaging: that CO(2) gas molecules present in solution only adsorb on silica when its surface is hydrophobic. More importantly, the results showed that gas adsorption/bubble growth undergoes two consecutive kinetic processes: a slow and a fast adsorption process.
Publisher: Elsevier BV
Date: 04-2017
Publisher: Informa UK Limited
Date: 11-2009
DOI: 10.5004/DWT.2009.795
Publisher: Wiley
Date: 07-03-2016
DOI: 10.1002/MMA.3858
Publisher: IWA Publishing
Date: 1998
Publisher: Elsevier BV
Date: 10-2014
Publisher: Elsevier BV
Date: 10-2014
Publisher: Elsevier BV
Date: 12-2014
Publisher: Informa UK Limited
Date: 02-2012
Publisher: Royal Society of Chemistry (RSC)
Date: 2018
DOI: 10.1039/C7EW00530J
Abstract: The effects of recycling spent filter backwash water (SFBW) on the removal of 14 organic pesticides were examined in a simulated conventional drinking water treatment process.
Publisher: IWA Publishing
Date: 2003
Abstract: The coagulation of a model seawater-humic acid solution with a hydrolysis metal salt (FeCl3) has been studied by monitoring floc size, solution pH, and zeta potential. The kinetic features of the orthokinetic coagulation have been demonstrated in relation to coagulant dosages, solution pH and zeta potential. Humic acid removal and floc charge reduction increased with coagulant dosage. Adjusting the solution pH prior to coagulation had a substantial effect on the treatment performance. By pH adjustment to pH 6, the greatest humic acid removal (by coagulation and subsequent membrane filtration) and the largest floc size was achieved at a FeCl3 dosage of 200 mmol l−1. It is believed that the coagulation is characterised by competition between OH- ions and humic acid for ferric ions in the co-precipitation process. In acidic pH, where the concentration of OH- ions is low, humic acid molecules may compete more favourably for bonding sites in the co-precipitation, which leads to a more compact precipitation and a higher overall humic acid removal.
Publisher: Informa UK Limited
Date: 07-10-2014
Publisher: Elsevier BV
Date: 2009
DOI: 10.1016/S1001-0742(09)60007-3
Abstract: Colloidal particle stability and some other interfacial phenomena are governed by interfacial force interactions. The two well known forces are van der Waals force and electrostatic force, as documented by the classical Derjaguin, Landau, Verwey, and Overbeek (DLVO) theory. Moreover, advances in modern instrumentation and colloid science suggested that some short-ranged forces or structure forces are important for relevant colloidal systems. The interfacial and/or molecular forces can be measured as a resultant force as function of separation distance by atomic force microscopy (AFM) colloid probe. This article presents a discussion on AFM colloid probe measurement of silica particle and silica wafer surfaces in solutions with some technical notifications in measurement and data convolution mechanisms. The measured forces are then analyzed and discussed based on the 'constant charge' and 'constant potential' models of DLVO theory. The difference between the prediction of DLVO theory and the measured results indicates that there is a strong short-range structure force between the two hydrophilic surfaces, even at extremely low ionic concentration, such as Milli-Q water purity solution.
Publisher: Elsevier BV
Date: 09-2003
Publisher: Royal Society of Chemistry (RSC)
Date: 2011
DOI: 10.1039/C1AY05122A
Publisher: Informa UK Limited
Date: 19-06-2017
DOI: 10.1080/09593330.2017.1329356
Abstract: The removal of glyphosate and aminomethylphosphonic acid (AMPA) with synthetic water was carried out on a lab-scale nanofiltration unit using two membranes, NFX and NFW. The presence of humic acid and some inorganic matters (CaCl
Publisher: Elsevier BV
Date: 11-2016
DOI: 10.1016/J.WATRES.2016.08.052
Abstract: Prechlorination is commonly used to minimize operational problems associated with biological growth as well as taste and odor control during drinking water treatment. However, prechlorination can also oxidise micropollutants into intermediate byproducts. This could impose profound effects on the safety of the finished water if the transformed byproducts are more toxic and less removable. This study investigated the effect of prechlorination on decomposition and subsequent removal of the four organophosphorus pesticides (OPPs): chlorpyrifos, diazinon, malathion and tolclofos-methyl using a simulated conventional water treatment process of powdered activated carbon assisted coagulation-sedimentation-filtration (PAC-CSF) and postchlorination. It was found that, following prechlorination, not only did the percentage of OPPs oxidation vary significantly, but also the concentration of transformed oxons, which are more toxic than their parent compounds, increased as the major identified oxidation byproducts in water. Removal of these oxons proved to be more difficult by the PAC-CSF than their parent OPPs, because they are more water soluble and more hydrophilic. Both the OPP oxidation and oxon formation increased with chlorine dose during prechlorination. Meanwhile, the continuing chlorination of OPPs by residual free chlorine during PAC-CSF further complicated the pesticide removal processes, generally resulting in a gradually increased formation of oxons. Moreover, in the final treatment stage of postchlorination, the more chlorine-reactive pesticides, malathion and diazinon, were completely oxidised and the formation of corresponding oxons was increased with the prechlorine dose. In contrast, a certain amount of the less chlorine-reactive pesticide tolclofos-methyl still remained in solution after postchlorination, accompanied by an increased formation of tolclofos-methyl oxon with prechlorine dose. Since the oxons are resistant to further oxidation and less adsorbable during the PAC-CSF process, the gross removal of these pesticides and their oxons decreased with increase of the prechlorine dose. This led to an accumulation of the more toxic oxons in the finished water, especially at higher chlorine doses during prechlorination. The significance of this work is the demonstration that, under circumstances where prechlorination is used and source water contains traces of OPPs, alternative practices should be prioritized to avoid the potential risks involved in consumption of the treated water.
Publisher: Mary Ann Liebert Inc
Date: 07-2016
Publisher: Elsevier BV
Date: 04-2019
Publisher: Elsevier BV
Date: 09-2016
Publisher: IWA Publishing
Date: 03-2012
Publisher: Elsevier BV
Date: 11-2019
DOI: 10.1016/J.CHEMOSPHERE.2019.06.058
Abstract: In drinking water treatment, complete mineralization of organophosphorus pesticides (OPPs) by UV-based advanced oxidation processes (UV AOPs) is rarely achieved. The formation of intermediate oxidation byproducts would likely have some profound effects on toxicity of the reaction solutions. This study investigated the intermediate oxidation byproducts, transformation pathway and toxicity of malathion solutions during the treatment processes of UV alone, UV/H
Publisher: Elsevier BV
Date: 02-2016
DOI: 10.1016/J.JHAZMAT.2015.10.021
Abstract: This study explored the efficacy and efficiency of a simultaneous UV-catalyzed oxidation-coagulation process of titanium sulfate (UV/Ti(SO4)2) for efficient removal of As(III) from water. It revealed that, As(III) could be oxidized to As(V) during the UV catalyzed coagulation of Ti(SO4)2 with highly efficient As(III) removal in the pH range 4-6. The UV catalyzed oxidation-coagulation showed surprisingly effective oxidation of As(III) to As(V) within a short time. XPS indicated that 84.7% of arsenic on the coagulated precipitate was in the oxidized form of As(V) after the UV/Ti(SO4)2 treatment of As(III) aqueous solutions at pH 5. Arsenic remaining in solution at high pH was in the oxidized form As(V). Removal efficiencies of As(III) were investigated as a function of pH, Ti(SO4)2 dosage, initial As(III) concentration and irradiation energy. As(III) could almost completely be removed (>99%) by the photocatalytic oxidation-coagulation process with a moderate dose of Ti(SO4)2 in the pH range 4-6 at an initial arsenic concentration of 200 μg/L. The mechanisms of the photocatalytic coagulation oxidation of Ti(SO4)2 are similar to those of UV/crystalline TiO2 particles, involving the formation and reactions of the hydroxyl radical OH and superoxide HO2/O2(-).
Publisher: Elsevier BV
Date: 06-2005
DOI: 10.1016/J.JCIS.2005.01.056
Abstract: The colloid stability of synthetic titania particles was studied as a function of KCl concentration at pH values of 6.3, 6.7, and 8.4, using static light scattering to obtain stability ratios. Standard DLVO theory was then used to calculate the stability ratios as a function of salt concentration. Reasonable agreement between theory and experiment could only be obtained if an effective interaction radius, corresponding to surface asperities on the titania particles, was used in the calculation. High-resolution TEM images suggest that the effective interaction radius corresponds to the size of surface crystallites formed during synthesis.
Publisher: Elsevier BV
Date: 08-2015
Publisher: Springer Science and Business Media LLC
Date: 09-01-2017
Publisher: Elsevier BV
Date: 02-1998
Publisher: Informa UK Limited
Date: 15-02-2013
Publisher: Royal Society of Chemistry (RSC)
Date: 2013
DOI: 10.1039/C3AY26402E
No related grants have been discovered for Jinming Duan.