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A type of biochar-supported iron phosphate nanoparticle stabilised by a sodium carboxymethyl cellulose (CMC@BC@ Fe3(PO4)2) composite was synthesised to remediate cadmium (Cd)-polluted soil. The surface morphology and functional groups of the composite were characterised by scanning electron microscopy and Fourier transform infrared spectrometry, respectively. Batch experiments showed that the composite (soil-to-solution ratio 1 g:10 mL) could effectively immobilise Cd in soil. The immobilisation efficiency of Cd was 81.3% after 28 days of remediation, and physiological-based extraction test bioaccessibility was reduced by 80.0%. The results of sequential extraction procedures indicated that the transformation from more easily extractable Cd to the least available form was responsible for the decrease in Cd bioavailability in soils. Plant growth experiments proved that the composite could inhibit Cd uptake to the belowground and aboveground parts of cabbage mustard by 44.8% and 70.2%, respectively, thus promoting cabbage mustard growth and development after remediation.

The magnetic Fe0@Fe3O4 nanocomposite was prepared and used to achieve the reductive/subsequent oxidative ring-opening of decabromodiphenyl ether (BDE209) in this work. The characterization results indicated that the structure of the composite consisted of small nanoscale zero-valent iron (nZVI) particles surrounding the surface of Fe3O4 nanoparticle (NP). A 100% removal efficiency and 80% degradation efficiency of BDE209 was reached by the composite accompanied with ultrasound(called NP/US system) for 36 h, which is higher than that obtained with conventional nZVI particles. Furthermore, the enhanced debromination and ring-opening of BDE209 was realized by a Fenton-like degradation process lasting for 12 h after the addition of H2O2 to the NP/US reaction at 36 h. Based on the degradation products identified, a two-stage reduction/oxidation degradation mechanism was proposed. During the first stage, which was reductive debromination, the major reductive activity of nZVI was efficiently enhanced in the presence of nano Fe3O4, which served as a catalyst to improve the stability of the nZVI nanoparticles and accelerate electron transfer, enhancing the degradation efficiency of BDE209. During the second stage, the oxidative ring-opening, the debromination products of BDE209 were proved to be attacked by abundant hydroxyl radicals generated both in the solution and on the surface of the Fe0@Fe3O4 nanoparticles. Thus, this work provides an efficient method to achieve the complete ring-opening of PBDEs using iron-based nanomaterials.

The difficulty of separating the powdered biochar from the environmental medium may lead to secondary pollution and hinder the large-scale application of biochar as an adsorbent. An effective strategy to solve this bottleneck is to introduce transition metals and their oxides into the biochar matrix, creating easily separable magnetic biochar. Magnetic biochar is also effective for the removal of pollutants from aqueous solution. This review comprises a systematic analysis of 109 papers published in recent years (From 2011 to June 2019), and summarises the synthetic methods and raw materials required for magnetic biochar preparation. The basic physicochemical properties of magnetic biochar are expounded, together with findings from relevant studies, and the application of magnetic biochar as an adsorbent or catalyst in environmental remediation are summarised. Other applications of magnetic biochar are also discussed. Finally, some constructive suggestions are given for the future direction of magnetic biochar research.

Exploiting the full potential of copper-based nanoparticles in the activation of peroxymonopersulfate (PMS) is a great challenge due to their insufficient dispersity and electronic properties. We report here a novel iron‑nitrogen co-doped carbon nanotube (FNC) modified with a Cu2O nanocomposite (Cu2O/FNC) that exhibits ultrahigh catalytic performance in the activation of PMS to degrade fluconazole (~95%). Catalytic performance evaluation illustrated that Cu2O/FNC also has wide pH applicability (3.0-11.0), long-term stability and excellent adaptability. In addition, luminescent bacteria toxicity tests confirm that Cu2O/FNC/PMS significantly reduced the acute biotoxicity of various recalcitrant pollutants (reduced by 45-83%). By identifying the reactive oxygen species (ROS) and catalytic performance for various pollutants, we propose that pollutants that interact weekly with activators are mostly destroyed by sulfate radicals and hydroxyl radicals, whilst both radical and non-radical routes were involved in the degradation of pollutants that were easily adsorbed. By modifying Cu2O with FNC, several crucial properties such as the specific surface area, surface defects, active sites and the charge transfer rate were significantly improved, leading to excellent catalytic performance for pollutant removal. Finally, a reasonable reaction mechanism is advanced for the fluconazole degradation pathway. This study not only develops a novel PMS oxidation system for fluconazole degradation, but also provides a new strategy to improve the reactivity and applicability of PMS activators by combining radical and non-radical activation pathways.

Common plasticizers and their alternatives are environmentally ubiquitous and have become a global problem. In this study, common plasticizers (phthalates and metabolites) and new alternatives [bisphenol analogs, t-butylphenyl diphenyl phosphate (BPDP), and bisphenol A bis(diphenyl phosphate) (BDP)] were quantified in urine and hair samples from children in Hong Kong, drinking water (tap water/bottled water) samples, and airborne particle samples from 17 kindergartens in Hong Kong. The results suggested that locally, children were exposed to various plasticizers and their alternatives. High concentrations of BPDP and BDP were present in urine, hair, tap water, bottled water, and air particulate samples. The geometric mean (GM) concentrations of phthalate metabolites in urine samples (126-2140 ng/L, detection frequencies 81%) were lower than those detected in Japanese and German children in previous studies. However, a comparison of the estimated daily intake values for phthalates in tap water [median: 10.7-115 ng/kg body weight bw/day] and air particles (median: 1.23-7.39 ng/kg bw/day) with the corresponding reference doses indicated no risk. Bisphenol analogs were detected in 15-64% of urine samples at GM concentrations of 5.26-98.1 ng/L, in 7-74% of hair samples at GM concentrations of 57.5-2390 pg/g, in 59-100% of kindergarten air samples at GM concentrations of 43.1-222 pg/m

Fruit peels were discarded as inevitable wastes in the production of fruit juice which wasted our resources and caused pollution problems. In this paper, iron nanoparticles were synthesized using Citrus maxima peel extracts to reduce Fe(III) in aqueous solution. The nanoparticles were characterized by TEM, EDS, XPS, FTIR, DLS and Zeta potential methods. Based on the characterization results, irregular iron nanoparticles with diameters of 10–100 nm were synthesized successfully. Moreover, the nanoparticles were mainly composed of Fe0 nanoparticles which were coated with various biomolecules from the extracts as capping or stabilizing agents.

Some problems exist in the current remediation of polybrominated diphenyl ethers (PBDEs) from aqueous solution by using iron-based nanoparticles. Our efforts have contributed to the synthesis of biochar-supported Ni/Fe bimetallic nanoparticle composites (BC@Ni/Fe). Under the optimum operating parameters of BC@Ni/Fe, the morphologic analysis revealed that biochar effectively solved the agglomeration of Ni/Fe nanoparticles and the removal efficiency of BDE209 obtained by BC@Ni/Fe (91.29%) was seven times higher than the sum of biochar (2.55%) and Ni/Fe (11.22%) in 10 min. The degradation products of BDE209 in the solution and absorbed on the BC@Ni/Fe were analyzed with gas chromatography-mass spectroscopy, which indicated that the degradation of BDE209 was mainly a process of stepwise debromination. Meanwhile, compared with Ni/Fe nanoparticles, the adsorption ability of the by-products of BDE209 by BC@Ni/Fe was greater, to a certain extent, which reduced the additional environmental burden. In addition, the concentration of nickle ion leaching from the Ni/Fe nanoparticles was 3.09 mg/L; conversely, the concentration of nickle leaching from BC@Ni/Fe was not detected. This excellent performance in our study indicates a possible means to enhance the reactivity and reduce the secondary risks of Ni/Fe nanoparticles.

In this study, soil culture experiments were conducted to explore the effects of biochar-supported Ni/Fe nanoparticles on the accumulation and translocation of polybrominated diphenyl ethers (PBDEs) in soil-plant system and its phytotoxicity to Brassica chinensis. Compared with those in BDE209 contaminated soils (S 1) and Ni/Fe nanoparticle-treated soil (S 3), the plant biomass, root, and shoot lengths in biochar-supported Ni/Fe nanoparticle-treated soil (S 4) were increased by 23 mg, 1.35 cm, and 2.08 cm and 27.2 mg, 1.75 cm, and 2.52 cm, respectively, suggesting that the phytotoxicity in S 4 treatment was significantly decreased. Moreover, in all treatments, the contents of BDE209, the total PBDEs, Ni, and Fe in sample plant tissues of S 4 were the lowest. In addition, the superoxide dismutase, peroxidase, and catalase activities in S 4 treatment were found to decrease by 33.8, 47.2, and 24.1%, respectively, compared to those in S 3. Results also showed that biochar addition not only reduced the uptake of PBDEs and heavy metals but also effectively improve soil fertility and reduce the leachability of Ni and Fe caused by Ni/Fe. Finally, the translocation factors (TFs) of PBDEs in four treatments followed the orders as S 1 > S 3 > S 4 > S 2, indicating that biochar has an inhibition effects on PBDE translocation in the plants. In summary, all of the results suggested that the phytotoxicity, translocation of PBDEs, and the negative effects caused by neat Ni/Fe nanoparticles in B. chinensis were decreased as a result of the effects of the biochar.

Benzophenones (BPs) and other ultra violet (UV) filters (UV-filters) are widely used in sunblock and other personal care products, raising concerns about their adverse health risks to human, especially for children. In the present study, BP-type UV-filters and other four widely used UV-filters were evaluated in the child urinary samples (4–6 years, n = 53), tap water and commercial distilled water in Hong Kong. The results suggested that the target chemicals are ubiquitous in the subject. BP1, BP2, BP3 and BP4 in children urine samples contributed closely to the overall children exposure of UV filters, with detection rates above 58% and geometric means ranging from 44.2 to 76.7 ng/mL. As a contrast, BP3 was the major substance found in the tap water and distilled bottle water, with detection rates of 100% and geometric means of 9.64 and 14.5 ng/L, respectively. There were some significant relationships between urinary UV filters and personal characteristics (BMI values, sex, income level, hand washing frequency, and body location usage), but the health risks associated with UV-filters in Hong Kong children might not be concerning. Only two children applied sun creams in this research, indicating that there were other sources to exposure these chemicals. Keywords: UV-filters, Urine, Children, Drinking water

Ni/Fe bimetallic nanoparticles were synthesized using biochar as a support (BC@Ni/Fe) and their effectiveness in removing BDE209 from soil was investigated. BET, SEM, TEM, XPS and FTIR were used to characterize the catalyst, and the efficiencies of biochar, Ni/Fe nanoparticles and BC@Ni/Fe for removing BDE209 from soil were compared. The results showed that Ni/Fe bimetallic nanoparticles highly dispersed in the biochar, reducing its agglomeration. Thus, the reaction activity of BC@Ni/Fe was increased. The removal efficiency of BDE209 by BC@Ni/Fe was 30.2% and 69% higher than that by neat Ni/Fe and biochar, respectively. Meanwhile, an enhanced degradation efficiency of PBDEs in soil was realized by monitoring the formation of Br⿿ ions with time in the system. In addition, the degradation products identified by GC⿿MS showed that the reductive degradation of BDE209 proceeded through stepwise or multistage debromination, for which the degradation pathways and removal mechanisms were speculated. Furthermore, BC@Ni/Fe reduced the bioavailability of metals in soil and adsorbed the degradation products of BDE209, representing an improvement over neat Ni/Fe nanoparticles for the remediation of PBDEs-contaminated soil.

Nano zero-valent iron (nZVI) and its modified nanomaterials are widely used in the degradation of some halogenated organic pollutants. In this study, we explored the effects of different proportions of tetrahydrofuran (THF) (50, 60, 70, 80, 90, and 100 %) on the degradation of decabromodiphenyl ether (BDE209) by Ni/Fe and nZVI nanoparticles with reference to the degradation kinetics, products, and pathway. The results illustrated that the effects of solvent on the degradation of BDE209 were similar when the two kinds of nanomaterials were used, although the Ni/Fe bimetallic nanoparticles exhibited a better catalytic activity compared with the pure nZVI during the degradation of BDE209. The apparent reaction rate constant (k obs) increased with the proportion of the water in the system, enhancing the degradation of BDE209. In terms of degradation products, a high proportion of THF led to an accumulation of higher-brominated BDEs, inhibiting the further debromination of BDE209. The inhibitory effect of the solvent (THF) can be explained that water played a role of hydrogen donor during the reductive degradation of BDE209 in the THF/water system. However, the proportion of THF in the degradation system posed no effect on the BDE209 debromination pathway and debromination location. The difficulty of para-debromination was observed in all of the solvent systems.

The potential for nanoscale phosphate amendments to remediate heavy metal contamination has been widely investigated, but the strong tendency of nanoparticles to form aggregates limits the application of this technique in soil. This study synthesized a composite of biochar-supported iron phosphate nanoparticle (BC@Fe3(PO4)2) stabilized by a sodium carboxymethyl cellulose to improve the stability and mobility of the amendment in soil. The sedimentation test and column test demonstrated that BC@Fe3(PO4)2 exhibited better stability and mobility than iron phosphate nanoparticles. After 28 days of simulated in situ remediation, the immobilization efficiency of Cd was 60.2 %, and the physiological-based extraction test bioaccessibility was reduced by 53.9 %. The results of sequential extraction procedures indicated that the transformation from exchangeable (EX) Cd to organic matter (OM) and residue (RS) was responsible for the decrease in Cd leachability in soil. Accordingly, the pot test indicated that Cd uptake by cabbage mustard was suppressed by 86.8 %. Compared to tests using iron phosphate nanoparticles, the addition of BC@Fe3(PO4)2 to soil could reduce the Fe uptake of cabbage mustard. Overall, this study revealed that BC@Fe3(PO4)2 could provide effective in situ remediation of Cd in soil.