Boron deficiency decreased the root activity of Ga-exposed rice seedlings by reducing iron accumulation and increasing Ga in iron plaque.

Gallium (Ga) is an emerging chemical pollutant chiefly associated with high-tech industries. Boron (B) alleviates the negative effects of toxic elements on plant growth. Thereby, the effects of B fertilization on Ga toxicity in rice seedlings was studied to clarify the role of iron plaque in the distribution of Ga, Fe, and B in Ga-treated rice seedlings in the presence or absence of B. Gallium exposure significantly reduced the biomass of rice seedlings. Boron deficiency induced a significant change in the distribution of B in Ga-treated rice seedlings compared with "Ga+B" treatments. Accumulation of Ga in roots, dithionite-citrate-bicarbonate (DCB) extracts, and shoots showed a dose-dependent manner from both +B and -B rice seedlings. Boron nutrition levels affect the distribution of Fe in roots, DCB extracts, and shoots, in which DCB-extractable Fe was significantly decreased from "Ga-B" treatments compared with "Ga+B" treatments. Root activity was significantly decreased in both Ga-exposed rice seedlings; however, B-deficient seedlings showed a severe reduction than +B rice seedlings. These results reveal that Fe plaque might be a temporary sink for B accumulation when plants are grown with proper B, wherein the re-utilization of DCB-extractable B stored in Fe plaque is mandatory for plant growth under B deficiency. Correlation analysis revealed that B deficiency decreased the root activity of Ga-exposed rice seedlings by reducing DCB-extractable Fe and increasing DCB-extractable Ga in Fe plaque. This study enhances our understanding of how B nutritional levels affect Ga toxicity in rice plants.

From nuclear track characterization to machine learning based image classification in neutron autoradiography for boron neutron capture therapy.

Knowledge of the 10B microdistribution is of great relevance in BNCT studies. Since 10B concentration assesment through neutron autoradiography depends on the correct quantification of tracks in a nuclear track detector, image acquisition and processing conditions should be controlled and verified, in order to obtain accurate results to be applied in the frame of BNCT. With this aim, an image verification process was proposed, based on parameters extracted from the quantified nuclear tracks. Track characterization was performed by selecting a set of morphological and pixel-intensity uniformity parameters from the quantified objects (area, diameter, roundness, aspect ratio, heterogeneity and clumpiness). Their distributions were studied, leading to the observation of varying behaviours in images generated by different samples and acquisition conditions. The distributions corresponding to samples coming from the BNC reaction showed similar attributes in each analyzed parameter, proving to be robust to the experimental process, but sensitive to light and focus conditions. Considering those observations, a manual feature extraction was performed as a pre-processing step. A Support Vector Machine (SVM) and a fully dense Neural Network (NN) were optimized, trained, and tested. The final performance metrics were similar for both models: 93%-93% for the SVM, vs 94%-95% for the NN in accuracy and precision respectively. Based on the distribution of the predicted class probabilities, the latter had a better capacity to reject inadequate images, so the NN was selected to perform the image verification step prior to quantification. The trained NN was able to correctly classify the images regardless of their track density. The exhaustive characterization of the nuclear tracks provided new knowledge related to the autoradiographic images generation. The inclusion of machine learning in the analysis workflow proves to optimize the boron determination process and paves the way for further applications in the field of boron imaging.

Boron stimulates fruit formation and reprograms developmental metabolism in sweet cherry.

Boron modulates a wide range of plant developmental processes; however, the regulation of early fruit development by boron remains poorly defined. We report here the physiological, anatomical, metabolic, and transcriptomic impact of pre-flowering boron supply on the sweet cherry fruit set and development (S1-S5 stages). Our findings revealed that endogenous boron content increased in early growth stages (S1 and S2 stages) following preflowering boron exogenous application. Boron treatment resulted in increased fruit set (S1 and S2 stages) and mesocarp cell enlargement (S2 stage). Various sugars (e.g., fructose and glucose), alcohols (e.g., myo-inositol and maltitol), organic acids (e.g., malic acid and citric acid), amino acids (e.g., valine and serine) accumulated in response to boron application during the various developmental stages (S1-S5 stages). Transcriptomic analysis at early growth (S1 and S2 stages) identified boron-responsive genes that are mainly related to secondary metabolism, amino acid metabolism, calcium-binding, ribosome biogenesis, sugar homeostasis and especially to photosynthesis. We found various boron-induced/repressed genes, including those specifically involved in growth. Several heat shock proteins displayed distinct patterns during the initial growth in boron-exposed fruit. Gene analysis also discovered several putative candidate genes like PavPIP5K9, PavWAT1, PavMIOX, PavCAD1, PavPAL1 and PavSNRK2.7, which could facilitate the investigation of the molecular rationale underlying boron function in early fruit growth. Substantial changes in the expression of numerous transcription factors, including PavbHLH25, PavATHB.12L, and PavZAT10.1,.2 were noticed in fruits exposed to boron. The current study provides a baseline of information for understanding the metabolic processes regulated by boron during sweet cherry fruit early growth and fruit development in general.

[Research on the formulation and revision of standard limits for antimony,boron and vanadium in the "Standards for Drinking Water Quality (GB5749-2022)" in China].

China is rich in antimony, boron, and vanadium mineral resources, which have been detected in environmental water bodies and drinking water. During the revision process of the "Standards for Drinking Water Quality (GB5749-2006)", research and evaluation are focused on three indicators: antimony, boron and vanadium. Vanadium is added and the limit value of boron is adjusted. This study reviews and discusses the technical contents related to the revision of the antimony, boron and vanadium, including the environmental presence levels, exposure status, health effects, and the revision of the standard limits of these three indicators. Suggestions are also made for the implementation of this standard.

New insights into the source of the boron memory effect and implications for accurate boron isotope measurements.

RATIONALE: The boron (B) memory effect is a concern for B isotope analysis in inductively-coupled plasma mass spectrometry and a potential cause of poor data comparability between laboratories. It is widely assumed that the memory resides in water droplets on the surface of the spray chamber. However, even without the use of the spray chamber, background subtractions are still required to generate accurate data, therefore additional causes for the memory effect exist, which are investigated here. METHODS: Different parts of the mass spectrometer were examined to pinpoint the source of a particularly high B background. After identifying the torch as the source of the background, different parts of the torch were soaked in dilute nitric acid, which was analyzed for B over time. RESULTS: B was leached out of the tip of the outer quartz tube of the torch in a fashion similar to borosilicate glass, which suggests the incorporation of B into the silica structure of the torch at high temperatures. Running 3% nitric acid washes effectively reduces the background. B background compositions change based on the solutions run beforehand, therefore different blank subtraction methods generate systematic differences. A new background subtraction method that utilizes B isotope ratios improved the precision by up to 0.14‰. The addition of a water wash step before sample elution led to smaller eluent volumes and improved matrix matching without causing a B breakthrough. CONCLUSIONS: An important part of the B memory derives from the torch glass, which incorporates B from sample solutions at high temperatures. Multiple nitric acid washes, matrix matching, blank subtraction, and standard sample bracketing generated accurate B isotope analyses with background/signal ratios as high as 10%, without the need for hazardous chemicals as washes. B isotope values of two sediment standards that represent average post-Archean continental crust were reported.

Matrix-independent boron isotope analysis of silicate and carbonate reference materials by ultraviolet femtosecond laser ablation multi-collector inductively coupled plasma mass spectrometry with application to the cold-water coral Desmophyllum dianthus.

RATIONALE: Boron isotopes are a powerful tool for pH reconstruction in marine carbonates and as a tracer for fluid-mineral interaction in geochemistry. Microanalytical approaches based on laser ablation multi-collector inductively coupled plasma mass spectrometry (LA-MC-ICP-MS) often suffer from effects induced by the sample matrix. In this study, we investigate matrix-independent analyses of B isotopic ratios and apply this technique to cold-water corals. METHODS: We employ a customized 193 nm femtosecond laser ablation system (Solstice, Spectra-Physics) coupled to a MC-ICP-MS system (Nu Plasma II, Nu Instruments) equipped with electron multipliers for in situ measurements of B isotopic ratios (11 B/10 B) at the micrometric scale. We analyzed various reference materials of silicate and carbonate matrices using non-matrix matched calibration without employing any correction. This approach was then applied to investigate defined increments in coral samples from a Chilean fjord. RESULTS: We obtained accurate B isotopic ratios with a reproducibility of ±0.9‰ (2 SD) for various reference materials including silicate glasses (GOR132-G, StHs6/80-G, ATHO-G and NIST SRM 612), clay (IAEA-B-8) and carbonate (JCp-1) using the silicate glass NIST SRM 610 as calibration standard, which shows that neither laser-induced nor ICP-related matrix effects are detectable. The application to cold-water corals (Desmophyllum dianthus) reveals minor intra-skeleton variations in δ11 B with average values between 23.01‰ and 25.86‰. CONCLUSIONS: Our instrumental set-up provides accurate and precise B isotopic ratios independently of the sample matrix at the micrometric scale. This approach opens a wide field of application in geochemistry, including pH reconstruction in biogenic carbonates and deciphering processes related to fluid-mineral interaction.

Removal of pollutants from aqueous product of Co-hydrothermal liquefaction: Adsorption and isotherm studies.

Hydrothermal liquefaction (HTL) is an attractive technology for the conversion of wet waste into biofuel and co-HTL has been touted to increase the quality of products. However, the recovery of energy from wastewater byproduct called aqueous co-product (ACP) is limited due to the presence of toxic inhibitory substances. Adsorption has been countenanced to remove these toxic compounds but there has not been a distinct comprehensive adsorption isotherm study to explain the interaction between the adsorbate molecules and the adsorbent sites. This study investigated the sorption mechanism of oxidizable reducing pollutants measured as chemical oxygen demand (COD); heavy metals (boron and copper); and phenols from ACP samples obtained from co-HTL of brewery trub (BT), and primary sludge (PS) onto granular and powdered activated carbon (GAC and PAC). Conventional isotherm models such as Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich were used for data analysis. Results indicated that the adsorptive capacity (qe) of PAC was greater than GAC in COD adsorption (BT-1947 > 234; BTPS-617 > 245; PS-289 > 207), boron adsorption (BTPS-70 > 7; PS-53 > 49), copper adsorption (BT-5 > 1; BTPS-3 > 2; PS-1.3 > 1.1) and phenol adsorption (BT-1340 > 356; BTPS-1587 > 253; PS-460 > 245) in mg/g, µg/g, µg/g, and µg/g respectively. Comparing the adsorption of pollutants onto PAC and GAC, this study observed that PAC followed the Temkin, and Dubinin-Radushkevich models in the adsorption of the four pollutants while GAC followed the Freundlich and Langmuir models in the adsorption of phenol and copper, and Temkin, and Dubinin-Radushkevich in the adsorption of COD and boron. This study proved that combining feedstock in HTL (co-HTL) does not only change the quality of the ACP but also changes the dynamics of the adsorption isotherms. The Free Energy Change (ΔG0) result showed a spontaneous reaction in the adsorption of copper and phenol. This study presents an adsorption equilibrium information for the interpretation of adsorption isotherms for the overall improvement of adsorption mechanism pathways and the effective design of adsorption systems for the treatment of ACP.

Changes in phytochemical composition of Merlot grape and wine induced by the direct application of boron.

In this study the effect of the direct application of different concentrations of boron in grape bunches on the phytochemical composition of grapes and wine was evaluated. The experiment was carried out by direct application to the grape bunch of different concentrations (0, 1.0, 2.0, 4.0 and 8.0 g/L) of boron solution, in two consecutive vintages, 2018 and 2019. The wines were elaborated by the same microvinification method. Histological analyzes by optical microscopy and phenolic profile by HPLC-DAD were performed on the grapes. The wines were analyzed by HPLC-DAD and ICP-MS for phenolic profile and elemental composition, respectively. Histological analyzes of the grape skin showed an increase in the presence of polyphenols in the cellular tissue of grapes treated with different concentrations of boron when compared to the control samples in both vintages. The addition of boron influenced the phenolic profile of the grapes, resulting in an increase in the content of anthocyanins and flavanols. Regarding to wines, the treatment of grapes by direct application of boron significantly influenced the chemical composition of wines. In 2018, the application of 2 g/L of boron showed a significant increase in the concentration of malvidin and delphinidin in wines. The application of 1 g/L showed the highest concentration of malvidin, delphinidin and peonidin in the 2019 vintage. The boron content increased in the wine samples according to the boron concentrations applied to the grape. Thus, it is possible to produce chemically distinct wines with the direct application of boron to the grapes.

Characterizing spatial dependence of boron, arsenic, and other trace elements for Permian groundwater in Northern Anhui plain coal mining area, China, using spatial autocorrelation index and geostatistics.

Anthropogenic and geological factors play an essential role in the variability of groundwater quality, resulting in a weak spatial dependence of groundwater trace elements. Thus, it is an essential study to investigate the factors affecting groundwater quality and its spatial abundance of trace elements (including As, B, and other metalloids). In this study, samples are obtained from a Permian sandstone fracture aquifer in a coal mining area. A multivariate statistical analysis, hydrogeochemistry modeling, and spatial autocorrelation analysis were used to analyze the data. The results showed that Moran index was positive for all trace elements, which had good spatial autocorrelation. The Local indicators of spatial association (LISA) indicated that trace elements were clustered. The hydrogeochemical modeling results indicated that the precipitation and stability of iron-phase minerals, such as rhodochrosite and arsenic (As) absorption on the surface of iron-phase minerals in the aquifer, may limit concentrations in the southern region. The spatial autocorrelations of both As and Boron (B) were positive (high-high) in the western areas, indicating that As contamination occurred from both natural geological causes and human coal mining activities. In contrast, B contamination was mainly linked to the influence of human agricultural or industrial activities. Over 96% of the groundwater concentrations of As (10 µg/L) and B (300 µg/L) in the study area exceeded World Health Organization (WHO) limits. Overall, the results of this work could help decision-makers involved in regional water quality management visualize disperse zones where specific anthropogenic and geological processes may threaten groundwater quality.

Life cycle assessment of a novel tannin-boron association for wood protection.

In these studies of fix boron compounds, associations between tannins and boron (TB) in the form of boric acid appear to be of interest. These TB associations allow the use of boron at very low levels (in compliance with EU restrictions, 2008/58/EC) and limit boron leaching which maintains biological resistance and fire retardant properties. As a consequence, TB wooden products present an extended service life compared to boron compounds alone and were designed to be environmentally-friendly wood protection systems. A follow-up of tannin­boron use identified the environmental impacts using a life cycle assessment (LCA). This LCA was performed on tannin­boron preservative products as well as several industrial preservative-treated timbers and concrete used in the landscape. Cr-containing inorganic salt and an alkaline copper quaternary preservative formulation, as well as concrete, have been used as referential materials to compare the environmental footprint with the tannin­boron treated system. A model was created with life cycle stages used to calculate inputs and outputs during raw material extraction, supplier transportation, manufacturing process, distribution, disposal transportation and processing. Tannin production data were based on Vieira et al. in the field of condensed tannin extraction. However, the extracted tannin in the extraction yield, the inorganic salt, and the process applied are not perfectly comparable with the extraction conditions industrially applied for the Mimosa (Acacia mearnsii) extract which is the major constituent of the TB formulations. The latter is counter-current water extracted without any chemicals or with a limited amount of NaHSO3 or Na2SO3 (at 0.5 % to 1 %) - at a temperature of 70-90 °C. Unfortunately these parameters cannot be elaborated by the LCA program because there is no data available for the production of Na bisulphite or Na bicarbonate in the LCI data used. Other input data were sourced from the ecoinvent v3.8 database. The ReCiPe midpoint method was used to assess the environmental footprint and the CED method was chosen to analyze a general view of the energy-related environmental impacts in the life cycle. Overall, the results demonstrated that tannin­boron preservatives can be regarded as a low-environmental impact formulation. Additionally, an economic analysis of the development of a commercially-viable tannin­boron preservative would now be timely.

Removal of pesticide residues from apple and tomato cuticle.

Pesticide residues are always an unsolved problem in the world despite all kinds of prevention measures. The present research work is based on a scientific hypothesis, i.e., "The removal of average pesticide residue is inversely proportional to the thickness of cuticle." The effects of boron-containing products and plant-based surfactants were tested for the removal of five pesticides (lambda-cyhalothrin, chlorpyrifos, diflubenzuron, metaflumizone, acetamiprid) on tomatoes and apples. Boron-containing products were able to remove the pesticide residues on average between 58.0 and 72.6% in tomatoes and 33.2-58.8% in an apple. While plant-based surfactants removed residues on average between 58.5 and 66.6% in tomatoes and 41.0-53.2% in an apple. The highest removal rate was 72% with etidot at 1%. The solution of 1% C8-C10 provided 66.6% average removal for tomatoes. Less removal was achieved in apples. For an apple, Log Kow and molecular mass (independent variables) were significant with p < 0.01, and the coefficient of determination (R2) was > 0.87. However, the multiple linear regression analysis for ground colemanite was significant with R2 of 0.96. In tomatoes, neither Log Kow nor molecular mass as significant. The correlation was found between the physical and chemical properties of pesticides, but it is estimated that the thickness of the cuticle is effective in removing pesticides.

Research on the formulation and revision of standard limits for antimony,boron and vanadium in the "Standards for Drinking Water Quality (GB5749-2022)" in China / 中华预防医学杂志

China is rich in antimony, boron, and vanadium mineral resources, which have been detected in environmental water bodies and drinking water. During the revision process of the "Standards for Drinking Water Quality (GB5749-2006)", research and evaluation are focused on three indicators: antimony, boron and vanadium. Vanadium is added and the limit value of boron is adjusted. This study reviews and discusses the technical contents related to the revision of the antimony, boron and vanadium, including the environmental presence levels, exposure status, health effects, and the revision of the standard limits of these three indicators. Suggestions are also made for the implementation of this standard.

Boron-doped titania for separation and purification of lactoferrin in dairy products.

Lactoferrin (LF), a natural iron regulating glycoprotein, exists in animal milk and plays multiple beneficial roles. Bovine LF is obtained by separation and purification from cow's milk, and has been added as a food additive to functional foods and infant formula now. Therefore, accurate analysis of LF in these foods is very important, but there are challenges such as poor selective extraction and separation efficiency. In this work, considering the cis-diol in LF, boron-doped titania (B-doped TiO2) material was prepared for selectively enrich LF from dairy products. In order to increase the saturation capacity of extracted LF, the amount of boron for doping was optimized, and maximum binding capacity of 63.9 mg g-1 was achieved when the atomic ratio of B to Ti was 1.65 with improved affinity in terms of KD value. In addition, the primary parameters affecting extraction efficiency such as extraction time, extraction pH, desorption time, and desorption solution were also optimized. The method of dispersive solid phase extraction based on B-doped TiO2 combined with ultra-high performance liquid chromatography-ultraviolet detection (UHPLC-UV) was developed and validated. The material greatly reduced the cost of sample pretreatment and the method also was applied to detect the LF in different dairy products such as liquid milk, fermented milk, and infant formula. This method could be used for routine analysis, separation and purification of LF.

Occurrence and distribution of heavy metals in water and soil sediments of Vellore District, Tamil Nadu, India.

The occurrence of heavy metals (HMs) in water and soil sediments represents a serious environmental concern. This study revealed the presence and distribution of HMs in water and soil sediments of various places in Vellore District, Tamil Nadu, India. Twenty-one sites were selected along the study area, and inductively coupled plasma-optical emission spectrometry (ICP-OES) was used to analyze the concentration of the heavy metals. The dominance of various HMs in the soil sediment sample follows the order strontium (Sr) > Manganese (Mn) > Barium (Ba) > Zinc (Zn) > Nickel (Ni) and Sr > Mn > Zn > Boron (B) > , respectively. It was found that the concentration of HMs in water and soil sediments in Ambur market and Mottukollai area was significantly higher than the recommended limits. Thus, the results showed that the presence of HMs in water and soil sediments could be threatened pollution factors unsafe for irrigation, drinking, and other human activities.

Effect of boron on cadmium uptake and expression of Cd transport genes at different growth stages of wheat (Triticum aestivum L.).

Boron (B) is an essential microelement for plant growth and has been shown to reduce cadmium (Cd) toxicity in wheat through modulating gene expression. However, there is not enough information about the effects of different applications of B fertilizer on the accumulation of Cd, particularly throughout the wheat growth period. This experiment employed two different B fertilization methods. The soil application method utilized 1.5 mg B kg-1 soil (Cd+B) and foliar application utilized 0.1% (F0.1%), 0.3% (F0.3%), and 0.6% (F0.6%) B concentrations along with 4 mg kg-1 Cd. The results showed that B application in the soil reduced Cd concentrations per plant by 43.9% at the seedling stage, 74.59% in the roots, and 52.11% in the shoots at the elongation stage. At the same time, Cd concentrations in the roots were higher by B application at the anthesis and maturity stages, suggesting that B retains more Cd in the roots. The gray correlation analysis showed that the gray relational coefficients followed the following order: F0.3% > F0.1% > Cd+B > F0.6%. According to quantitative real-time PCR analysis, the six Cd transporters were mostly expressed in the roots at the seedling stage and anthesis stage. In addition, the expression of TCONS1113, TRIAE1060, and TRIAE5370 showed a negative correlation relationship with Cd concentration at the seedling stage, both in roots and shoots. At the anthesis stage, the expression of TCONS1113 and TRIAE5370 in roots was higher in Cd-treated plants compared to B-treated plants, and a similar tendency was noted for the expression of TRIAE5770 and TRIAE1060 in shoots as well. These results suggest that B application could significantly inhibit Cd uptake and translocation by regulating the expression of Cd transporter genes, especially at the seedling stage and the elongation phase in wheat.

Advances in Technologies for Boron Removal from Water: A Comprehensive Review.

Boron overabundance in aquatic environment raises severe concerns about the environment and human health because it is toxic to various crops and induces many human and animal diseases with long-term consequences. In response to the boron pollution of water resources and the difficulty of eliminating boron from water for production and living purposes, this article summarizes the progress in research on boron removal technology, addressing the following aspects: (1) the reasons for the difficulty of removing boron from water (boron chemistry); (2) ecological/biological toxicity and established regulations; (3) analysis of different existing processes (membrane processes, resin, adsorption, chemical precipitation, (electric) coagulation, extraction, and combined methods) in terms of their mechanisms, effectiveness, and limitations; (4) prospects for future studies and possible improvements in applicability and recyclability. The focus of this paper is thus to provide a comprehensive summary of reported deboronation processes to date, which will definitely identify directions for the development of boron removal technology in the future.

Design of a DT neutron source based PGNAA facility for element determination in aqueous solution.

A DT neutron source-based prompt gamma ray neutron activation (PGNAA) facility for bulk sample analysis was designed and developed in this research. The aqueous samples containing chlorine and boron with known concentration were determined for the calibration curve by the facility. The neutron self-shielding effect was corrected by internal standard method. The minimum detectable concentration of boron and chlorine are 1.37 ± 0.42 and 12.51 ± 3.80 mg/L, respectively. Finally, five mixture aqueous solution samples were measured for the facility performance test. The maximum relative deviation of boron and chlorine are 4.49% and 5.32% respectively.

Rate, Efficiency, and Mechanisms of Electrochemical Perfluorooctanoic Acid Degradation with Boron-Doped Diamond and Plasma Electrodes.

The removal of per- or polyfluorinated alkyl substances (PFAS) has received increasing attention because of their extreme stability, our increasing awareness of their toxicity at even low levels, and scientific challenges for traditional treatment methods such as separation by activated carbon or destruction by advanced oxidation processes. Here, we performed a direct and systematic comparison of two electrified approaches that have recently shown promise for effective degradation of PFAS: plasma and conventional electrochemical degradation. We tailored a reactor configuration where one of the electrodes could be a plasma or a boron-doped diamond (BDD) electrode and operated both electrodes galvanostatically by continuous direct current. We show that while both methods achieved near-complete degradation of PFAS, the plasma was only effective as the cathode, whereas the BDD was only effective as the anode. Compared to the BDD, plasma required more than an order of magnitude higher voltage but lower current to achieve similar degradation efficiency with more rapid degradation kinetics. All these factors considered, it was noted that plasma or BDD degradation resulted in similar energy efficiencies. The BDD electrode exhibited zero-order kinetics, and thus, PFAS degradation using the conventional electrochemical method was kinetically controlled. On the contrary, analysis using a film model indicated that the plasma degradation kinetics of PFAS using plasma were mass-transfer-controlled because of the fast reaction kinetics. With the help of a simple quantitative model that incorporates mass transport, interfacial reaction, and surface accumulation, we propose that the degradation reaction kinetically follows an Eley-Rideal-type mechanism for the plasma electrode, and an intrinsic rate constant of 2.89 × 108 m4 mol-1 s-1 was obtained accordingly. The investigation shows that to realize the true kinetic potential of plasma degradation for water treatment, mass transfer to the interface must be enhanced.

Electrochemical oxidation of landfill leachate using boron-doped diamond anodes: pollution degradation rate, energy efficiency and toxicity assessment.

Electrochemical oxidation (EO), due to high efficiency and small carbon footprint, is regarded as an attractive option for on-site treatment of highly contaminated wastewater. This work shows the effectiveness of EO using three boron-doped diamond electrodes (BDDs) in sustainable management of landfill leachate (LL). The effect of the applied current density (25-100 mA cm-2) and boron doping concentration (B/C ratio: 500 ppm, 10,000 ppm and 15,000 ppm) on the performance of EO was investigated. It was found that, of the electrodes used, the one most effective at COD, BOD20 and ammonia removal (97.1%, 98.8% and 62%, respectively) was the electrode with the lowest boron doping. Then, to better elucidate the ecological role of LLs, before and after EO, cultivation of faecal bacteria and microscopic analysis of total (prokaryotic) cell number, together with ecotoxicity assay (Daphnia magna, Thamnocephalus platyurus and Artemia salina) were combined for the two better-performing electrodes. The EO process was very effective at bacterial cell inactivation using each of the two anodes, even within 2 h of contact time. In a complex matrix of LLs, this is probably a combined effect of electrogenerated oxidants (hydroxyl radicals, active chlorine and sulphate radicals), which may penetrate into the bacterial cells and/or react with cellular components. The toxicity of EO-treated LLs proved to be lower than that of raw ones. Since toxicity drops with increased boron doping, it is believed that appropriate electrolysis parameters can diminish the toxicity effect without compromising the nutrient-removal and disinfection capability, although salinity of LLs and related multistep-oxidation pathways needs to be further elucidated.

Efficient sequestration of boron from liquid phase by amidoxime-functionalized poly(acrylonitrile-co-acrylic acid): experimental and modelling analyses.

This study aims to produce amidoxime-modified poly(acrylonitrile-co-acrylic acid) using an optimized method and to investigate the performance of amidoxime-modified poly(acrylonitrile-co-acrylic acid) on the adsorption of boron ions in batch operations. Batch adsorption was conducted at the physiochemical parameters of pH, adsorbent dosage, and initial boron concentration. The isotherms and kinetics of adsorption data were studied at various initial boron concentrations. The renewed synthesis process gave a production yield of 77%, and the conversion of nitrile group to amidoxime was 78%. The adsorption reached its optimum point at pH = 8, adsorbent dosage = 4 g·L-1, and initial adsorbent concentration at 40 ppm. The best model fits for isotherm adsorption was the Sips model with heterogeneity factor (n) = 0.7611. In the kinetic study, the adsorption data fitted best with pseudo-second-order model. The synthesized polymeric adsorbent could be recycled with little decline in its boron entrapment capacities. Hence, amidoxime-modified poly(acrylonitrile-co-acrylic acid) exhibited high adsorption capacity and could be potentially explored as an alternative to commercial resin in the removal of boron from wastewater.