Synthesis of CaCO3 supported nano zero-valent iron-nickel nanocomposite (nZVI-Ni@CaCO3) and its application for trichloroethylene removal in persulfate activated system.

Nano zero-valent (nZVI) based composite have been widely utilized in environmental remediation. However, the rapid agglomeration and quick deactivation of nZVI limited its application on large scale. In this work, CaCO3 supported nZVI-Ni catalyst, namely nZVI-Ni@CaCO3 was prepared and used for the efficient removal of trichloroethylene (TCE) in PS oxidation process. The successful disbursement of nZVI-Ni on CaCO3 support material not only increased the surface area of nZVI-Ni@CaCO3 (69.45 m2/g) with respect to CaCO3 (5.92 m2/g) and bare nZVI (13.29 m2/g) but also improved the catalytic activity. XRD, XPS and FTIR analysis confirmed the successful formation of nZVI-Ni@CaCO3 nanoparticles. The nZVI-Ni@CaCO3 nanoparticles combined with PS had achieved complete removal of TCE (99.8%) with dosage of 36 mg/L and 1.34 mM respectively. These results showed that the use of CaCO3 as support material for nZVI-Ni could have significant influence on contaminant removal process. Scavenging and EPR tests validated the existence of SO4•-, OH• and O2•- radicals in PS/nZVI-Ni@CaCO3 system and highlighted the dominant role of SO4•- radicals in TCE removal process. HCO3- ions and humic acid have shown adverse effect on TCE removal due to radical scavenging and buffering effect. Owing to improved catalytic activity and easy preparation, the nZVI-Ni@CaCO3 nanoparticles could be served as an alternative strategy for environmental remediation.

Advances in sustainable approaches utilizing orange peel waste to produce highly value-added bioproducts.

Orange peel waste (OPW), a discarded part of orange fruit, is a rich source of essential constituents that can be transformed into highly value-added bioproducts. OPW is being generated in million tonnes globally and returns to the environment without complete benefit. Thus, a high volume of annually produced OPW in the industry requires effective valorization. In this regard, limited data is available that summarizes the broader spectrum for the sustainable fate of OPW to produce value-added bioproducts. The main objective of this treatise is to explore the sustainable production of bioproducts from OPW. Therefore, this review covers all the aspects of OPW, from its production to complete valorization. The review encompasses the extraction technologies employed for extracting different valuable bioactive compounds, such as: essential oil (EO), pectin, and carotenoids, from OPW. Furthermore, the suitability of bioconversion technologies (digestion/fermentation) in transforming OPW to other useful bioproducts, such as: biochemicals (lactic acid and succinic acid), biopolysaccharides (xanthan and curdlan gum), and bioenergy (biomethane and bioethanol) is discussed. Also, it includes the concept of OPW-based biorefineries and their development that shall play a definite role in future to cover demands for: food, chemicals, materials, fuels, power, and heat. Lastly, this review focuses on OPW-supplemented functional food products such as: beverages, yogurts, and extruded products. In conclusion, insights provided in this review maximize the potential of OPW for commercial purposes, leading to a safe, and waste-free environment.

Urchin-like magnetic microspheres for cancer therapy through synergistic effect of mechanical force, photothermal and photodynamic effects.

BACKGROUND: Magnetic materials mediated by mechanical forces to combat cancer cells are currently attracting attention. Firstly, the magnetic force penetrates deeper into tissues than the NIR laser alone to destroy tumours. Secondly, the synergistic effect of nano-magnetic-material characteristics results in a viable option for the targeted killing of cancer cells. Therefore, mechanical force (MF) produced by magnetic nanomaterials under low frequency dynamic magnetic field combined with laser technology is the most effective, safe and efficient tool for killing cancer cells and tumour growth. RESULTS: In this study, we synthesized novel urchin-like hollow magnetic microspheres (UHMMs) composed of superparamagnetic Fe3O4. We demonstrated the excellent performance of UHMMs for killing laryngocarcinoma cancer cells through mechanical force and photothermal effects under a vibrating magnetic field and near-infrared laser, respectively. The killing efficiency was further improved after loading the synthesised UHMMs with Chlorin e6 relative to unloaded UHMMs. Additionally, in animal experiments, laryngocarcinoma solid tumour growth was effectively inhibited by UHMMs@Ce6 through magneto-mechanic force, photothermal and photodynamic therapy. CONCLUSIONS: The biocompatibility and high efficiency of multimodal integrated therapy with the UHMMs prepared in this work provide new insights for developing novel nano therapy and drug loading platforms for tumour treatment. In vivo experiments further demonstrated that UHMMs/Ce6 are excellent tools for strongly inhibiting tumour growth through the above-mentioned characteristic effects.

Development of a novel noninvasive quantitative method to monitor Siraitia grosvenorii cell growth and browning degree using an integrated computer-aided vision technology and machine learning.

The rapid, accurate and noninvasive detection of biomass and plant cell browning can provide timely feedback on cell growth in plant cell culture. In this study, Siraitia grosvenorii suspension cells were taken as an example, a phenotype analysis platform was successfully developed to predict the biomass and the degree of cell browning based on the color changes of cells in computer-aided vision technology. First, a self-made laboratory system was established to obtain images. Then, matrices were prepared from digital images by a self-developed high-throughput image processing tool. Finally, classification models were used to judge different cell types, and then a semi-supervised classification to predict different degrees of cell browning. Meanwhile, regression models were developed to predict the plant cell mass. All models were verified with a good agreement by biological experiments. Therefore, this method can be applied for low-cost biomass estimation and browning degree quantification in plant cell culture.

Removal of levofloxacin from aqueous solution by green synthesized magnetite (Fe3O4) nanoparticles using Moringa olifera: Kinetics and reaction mechanism analysis.

Levofloxacin antibiotic is frequently being detected in the environment and regarded as an emerging contaminant. The present study was focused on the green synthesis of magnetite (Fe3O4 - gINPs) nanoparticles from Moringa olifera and its efficiency for removal of levofloxacin from aqueous solution. The adsorbent magnetite nanoparticles (Fe3O4) were prepared by green synthesis using Moringa olifera and coprecipitation method. Characterizations analyses of both chemically and green synthesized nanoparticles were performed by SEM, XRD, and FTIR. The average crystallite size of gINPs was 14.34 nm and chemically synthesized was 18.93 nm. The performance of the synthesized product was evaluated by adsorption capacity and removal efficiency. The parameters considered included adsorbent (gINPs) dosage, initial concentration of adsorbate, pH, contact time, and temperature. The obtained data were fitted to kinetic and isotherm models to determine the mechanism. Adsorption batch experiments were conducted to determine the reaction mechanism by studying kinetics while fitting isotherm models for samples analyzed using HPLC at 280 nm. Results showed that 86.15% removal efficiency of 4 mg L-1 levofloxacin was achieved by 100 mg L-1 gINPs in 24 h contact time when all other parameters (pH 7, temperature 25 °C) were kept constant. The maximum adsorption capacity achieved at equilibrium was 22.47 mg/g. Further, it was identified as a pseudo-second-order model with R2 = 0.965 for adsorption kinetics while isotherm data better fitted to the Freundlich model compared to Langmuir isotherm with R2 = 0.994. The potential pathway determined for levofloxacin removal was chemisorption with minor diffusion, multilayer, spontaneous and exothermic processes on the gINPs (Fe3O4). Reusability experiments were conducted in four cycles and removal efficiency varied from 85.35% to 80.47%, indicating very high potential of the adsorbent for re-use.

Ecotoxicity of Caenorhabditis elegans following a step and repeated chronic exposure to tetrabromobisphenol A.

To better understand the toxicity of tetrabromobisphenol A (TBBPA), its effects on the model nematode Caenorhabditis elegans were investigated. Following a step and repeated chronic exposure from L4-larvae to day-10 adult, physiology endpoints (growth and locomotion behaviors including head thrashes, body bends and pumping rate), biochemical endpoints (reactive oxygen species, superoxide dismutase activity, catalase activity), and molecular stress-related gene expression were tested at environmentally relevant concentrations of TBBPA (0.01-100 µg/L). The results showed that concentrations of TBBPA greater than 10 µg/L, clearly influenced the physiology behaviors (growth and locomotion endpoints). Under repeated exposure, C. elegans exhibited adaptive responses in head thrashes and pumping rate. Compared to toxicity evaluation following repeated chronic exposure, a significantly greater response was induced at the same concentration following a step chronic exposure. Reactive oxygen species production was significantly enhanced following a step and repeated TBBPA exposure at the concentrations of 1 and 10 µg/L, respectively. qRT-PCR showed that ctl-1, ctl-2, ctl-3 and sod-3 expression significantly increased, which was obviously correlated with physiological and biochemical behaviors under both treatment conditions according to Pearson correlation test analysis. sod-3 and ctl-2 mutations were more sensitive than the wild-type N2 under a step chronic TBBPA exposure at a level of 10 µg/L. Thus, chronic exposure to TBBPA induces an oxidative stress response in C. elegans, with ctl-2 and sod-3 playing a vital role in TBBPA-induced toxicity in nematodes.

Feasibility Study of Anaerobic Baffled Reactor Coupled with Anaerobic Filter Followed by Membrane Filtration for Wastewater Treatment.

The performance of a Decentralized Wastewater Treatment System (DWTS) comprising an Anaerobic Baffled Reactor (ABR) and an Anaerobic Filter (AF) and Membrane Filtration (MF) module was studied for domestic wastewater treatment. The efficiency of the system was evaluated by running ABR at four different HRTs (14, 12, 10, and 8 h) resulting in COD removal efficiencies of 74, 72, 69, and 65%, respectively. The performance of AF using four different filtration media, i.e., PVC pipe (25 mm), PVC pipe (20 mm), PVC pipe (15 mm), and Kaldnes K3, was determined at optimized HRT (12 h). Among all the filtration media tested, the highest performance efficiency of the system was found with the PVC pipe (20 mm), which showed COD, TP, and TKN removal of 79, 32, and 63%, respectively. The efficacy of the system was proven via significant COD and turbidity removal of 94.6 and 87.2%, respectively, by the combined system.

Multiscale engineering of microbial cell factories: A step forward towards sustainable natural products industry.

Microbial cell factories (bacteria and fungi) are the leading producers of beneficial natural products such as lycopene, carotene, herbal medicine, and biodiesel etc. These microorganisms are considered efficient due to their effective bioprocessing strategy (monoculture- and consortial-based approach) under distinct processing conditions. Meanwhile, the advancement in genetic and process optimization techniques leads to enhanced biosynthesis of natural products that are known functional ingredients with numerous applications in the food, cosmetic and medical industries. Natural consortia and monoculture thrive in nature in a small proportion, such as wastewater, food products, and soils. In similitude to natural consortia, it is possible to engineer artificial microbial consortia and program their behaviours via synthetic biology tools. Therefore, this review summarizes the optimization of genetic and physicochemical parameters of the microbial system for improved production of natural products. Also, this review presents a brief history of natural consortium and describes the functional properties of monocultures. This review focuses on synthetic biology tools that enable new approaches to design synthetic consortia; and highlights the syntropic interactions that determine the performance and stability of synthetic consortia. In particular, the effect of processing conditions and advanced genetic techniques to improve the productibility of both monoculture and consortial based systems have been greatly emphasized. In this context, possible strategies are also discussed to give an insight into microbial engineering for improved production of natural products in the future. In summary, it is concluded that the coupling of genomic modifications with optimum physicochemical factors would be promising for producing a robust microbial cell factory that shall contribute to the increased production of natural products.

Enhancement in reactivity via sulfidation of FeNi@BC for efficient removal of trichloroethylene: Insight mechanism and the role of reactive oxygen species.

A novel catalyst of sulfidated iron-nickel supported on biochar (S-FeNi@BC) was synthesized to activate persulfate (PS) for the removal of trichloroethylene (TCE). A number of techniques including XRD, SEM, TEM, FTIR, BET and EDS were employed to characterize S-FeNi@BC. The influence of sulfur to iron ratio (S/F) on TCE removal was investigated by batch experiments and a higher TCE removal (98.4%) was achieved at 0.22/1 ratio of S/F in the PS/S-FeNi@BC oxidation system. A dominant role in iron species conversion was noticed by the addition of sulfur in FeNi@BC system. Significant enhancement in recycling of the dissolved and surface Fe(II) was confirmed which contributed to the generation of free and surface-bound active radical species (OH, O2-, 1O2, SO4-). Further, the presence and contribution of these radicals were validated by the electron paramagnetic resonance (EPR) and quenching study. In addition, XPS results demonstrated the dominant role of S(-II) with the increase of Fe(II) from 36.3% to 58.6% and decrease of Fe(III) from 52.1% to 39.8% in the PS/S-FeNi@BC system. In crux, the influence of initial pH, catalyst dosage, oxidant dosage, and inorganic ions (HCO3-, Cl-, NO3- and SO42-) on TCE removal was also investigated. The findings obtained from this study suggest that S-FeNi@BC is an appropriate catalyst to activate PS for TCE contaminated groundwater remediation.

Rationally optimized generation of integrated Escherichia coli with stable and high yield lycopene biosynthesis from heterologous mevalonate (MVA) and lycopene expression pathways.

The stability and high productivity of heterogeneous terpenoid production in Escherichia coli expression system is one of the most key issues for its large scale industrialization. In the current study on taking lycopene biosynthesis as an example, an integrated Escherichia coli system has been generated successfully, which resulted into stable and high lycopene production. In this process, two modules of mevalonate (MVA) pathway and one module of lycopene expression pathway were completely integrated in the chromosome. Firstly, the copy number and integrated position of three modules of heterologous pathways were rationally optimized. Later, a strain DH416 equipped with heterogeneous expression pathways through chromosomal integration was efficiently derived from parental strain DH411. The evolving DH416 strain efficiently produced the lycopene level of 1.22 g/L (49.9 mg/g DCW) in a 5 L fermenter with mean productivity of 61.0 mg/L/h. Additionally, the integrated strain showed more genetic stability than the plasmid systems after successive 21st passage.

Kinetically modelled approach of xanthan production using different carbon sources: A study on molecular weight and rheological properties of xanthan.

The present study emphasizes improving the overall yield, productivity and quality of xanthan by Xanthomonas campestris using different carbon sources via optimizing the fermentation media and kinetic modelling work. After optimization, six carbon sources and one nitrogen source were selected for xanthan production in 5 L bioreactor. Kinetic modelling was applied to assess the experimental fermentation data and to check its influence on scale-up production. In this work, xanthan production reached 40.65 g/L with a growth-associated rate constant (α) of 2.831, and highest specific growth rate (µm) of 0.37/h while using maltose as the sole carbon source. Furthermore, rheological properties were determined, and Herschel-Bulkley model was employed to assess the experimental data. Interestingly, xanthan obtained from sucrose and glucose showed the highest yield stress (τ0) of 12.50 ± 0.31 and 7.17 ± 0.21. Moreover, the highest xanthan molecular weight of 3.53 × 107 and 3.25 × 107 g/mol were also found with sucrose and glucose. At last, the proposed mechanism of sugar metabolism and xanthan biosynthesis pathway were described. Conclusively, maltose appeared as the best carbon source for maximum xanthan production: while sucrose and glucose gave qualitatively best results. In short, this systematically modelled approach maximizes the potential output and provides a solid base for continuous cultivation of xanthan at large-scale production.

Bimetallic Doped RuO2 with Manganese and Iron as Electrocatalysts for Favorable Oxygen Evolution Reaction Performance.

Synthesizing oxygen evolution reaction (OER) catalysts with enhanced activity by codoping has been proven to be a feasible approach for the efficient use of noble metals via renewing their basic intrinsic properties. In continuation of the research in codoping, we prepare a ruthenium-based bimetallic doped catalyst Mn x Fe y Ru1-x-y O2 with an outstanding OER activity as compared to pure RuO2, one of the state-of-the-art OER catalysts. The synthesized codoped RuO2 with a Mn/Fe molar ratio of 1 reflected a Tafel slope of only 41 mV dec-1, which is appreciably lower than 64 mV dec-1 for pure RuO2. The X-ray photoelectron spectroscopy (XPS) performed reveals that oxygen vacancy and manganese valency are the key factors of the OER activity for codoped catalysts.

Xanthan-Curdlan nexus for synthesizing edible food packaging films.

In this study, we prepared a series of edible blend films of xanthan and curdlan by mixing different ratios of these two biopolymers. Characterization techniques like FTIR, XRD, TGA and SEM analysis were applied to investigate the newly formed films. Moreover, mechanical properties, moisture absorbance properties and water solubility of these films were also determined. The obtained results demonstrated that the strong intermolecular hydrogen bonding was observed between xanthan and curdlan at pH 5. At this pH, the xanthan-curdlan hydrogel retained the original structure of xanthan and sustained self-aggregation of xanthan chains via hydrogen bonding, which led to strong intermolecular bonding between xanthan and curdlan. Furthermore, the 5:5 and 4:6 ratios of xanthan and curdlan showed greater interaction in the blend films that resulted in their excellent miscibility. Moreover, highest tensile strength of 28.13 and 26.45 MPa were also found in the same rational of XG/CG blend films. In addition, it was observed that the curdlan incorporation improved the water solubility properties of XG/CG blend films. Conclusively, this xanthan/curdlan nexus with excellent mechanical and moisture barrier properties confirm its potential application and prospective use as food packaging material.

The impact of surface properties and dominant ions on the effectiveness of G-nZVI heterogeneous catalyst for environmental remediation.

The surface properties of nanocomposites are influenced by the existence of inorganic species that may affect its performance for specific catalytic applications. The impact of different ionic species on particular catalytic activity had not been investigated to date. In this study, the surface charge (zeta potential) of graphene-oxide-supported nano zero valent iron (G-nZVI) was tested in definitive cationic (Na+, K+, Ca2+ and Mg2+) and anionic (Br-, Cl-, NO3-, SO42-, and HCO3-) environments. The efficiency of G-nZVI catalyst was inspected by measuring the generation of reactive oxygen species (ROS) for the degradation of 1,1,1-trichloroethane (TCA) in sodium percarbonate (SPC) system. Tests conducted using probe compounds confirmed the generation of OH and O2- radicals in the system. In addition, the experiments performed using scavenging agents certified that O2- were primary radicals responsible for TCA removal, along with prominent contribution from OH radicals. The study confirmed that G-nZVI catalytic capability for TCA degradation is notably affected by various cationic species. The presence of Ni2+ and Cu2+ significantly enhanced (94%), whereas Na+ and K+ had minor effects on TCA removal. Overall, the results indicated that groundwater ionic composition may have low impact on the effectiveness of G-nZVI-catalyzed peroxide TCA treatment.

A promising engineering strategy for water electro-oxidation iridate catalysts via coordination distortion.

Here, we study the relationship between the coordination structure of IrO6 and OER activity in a wide range of oxides with systematic comparisons. The results reveal that distorted IrO6 is more conducive to OER activity. Specifically, for a given material, regulating the transformation of the IrO6 octahedron from D4h compression to D4h elongation causes electrons near the EF level to become more delocalized, which is very beneficial for reducing the energy of the rate determining step. Our findings will guide the design and preparation of more efficient iridium-based OER catalysts.

Highly Efficient Oxygen Evolution Activity of Ca2IrO4 in an Acidic Environment due to Its Crystal Configuration.

We systematically characterized the perovskite-like oxides Ca2IrO4 and CaIrO3 as the oxygen evolution reaction (OER) catalysts. Compared with IrO2, universally accepted as the current state-of-the-art OER catalyst, Ca2IrO4 showed an excellent OER catalytic activity in an acidic environment, whereas CaIrO3 did not. X-ray photoelectron spectroscopy (XPS) spectra showed that the oxidation of iridium in Ca2IrO4 and CaIrO3 was slightly beyond +4. X-ray absorption near-edge structure (XANES) spectra illustrated that the IrO6 octahedral geometric structure in Ca2IrO4 and CaIrO3 showed differences. The IrO6 octahedral is asymmetrically distorted and uniformly compressed in Ca2IrO4 and CaIrO3. Therefore, we propose that the IrO6 octahedral distortion plays an important role in the OER activities.

Effect of lattice strain on the electro-catalytic activity of IrO2 for water splitting.

The lattice strain of IrO2 plays a critical role in determining its OER activity. The Ir-O bond length change in IrO6 coordination induces lattice strain. Increasing the annealing temperature results in a stretching strain along the c axis and a compressive strain on the a and b axes, leading to a larger c/a ratio. Enhancing the lattice strain decreases the c/a ratio, which is beneficial for improving OER activity.

Optimized biosynthesis of xanthan via effective valorization of orange peels using response surface methodology: A kinetic model approach.

Herein, an enhanced green production of xanthan gum has been achieved by utilizing orange peels. Response surface methodology and kinetic modeling were adapted for the process optimization and its influence on scale up production respectively. Optimal conditions for the maximum xanthan production were 1.62% acid hydrolysis, 85% carbon source of orange peel hydrolysate and 30.4°C temperature. Furthermore, the optimized treatment was conducted in the batch culture fermentor to observe the associated variations during scale up process. In bio-fermentor, to the first time ever, xanthan production along with reducing sugar conversion and utilization rates reached 30.19g/L, 69.29% and 99.99%, respectively. Employed characterization techniques of FTIR, XRD and HPLC confirmed the fermented product as xanthan gum and obtained an average molecular weight of 1.01×106g/mol. This work on account of optimized process parameters presented maximum xanthan production from a waste material.

Cultivating crystal lattice distortion in IrO2via coupling with MnO2 to boost the oxygen evolution reaction with high intrinsic activity.

Here, we report an effective strategy to lower Ir consumption and boost the OER performance in acid by loading IrO2 onto MnO2, in which the IrO2 crystals are well dispersed and undergo a so-called z-extension Jahn-Teller distortion in the octahedral structure. Compared with IrO2, the mass activity and intrinsic activity for IrO2/MnO2 were largely increased.

Enhanced effect of EDDS and hydroxylamine on Fe(II)-catalyzed SPC system for trichloroethylene degradation.

This study presents a performance comparison of Fe(II)-catalyzed sodium percarbonate (SPC), Fe(II)-EDDS-catalyzed SPC, and of the innovative hydroxylamine hydrochloride (HA)-Fe(II)-EDDS-catalyzed SPC for the degradation of trichloroethylene (TCE) in water. TCE degradation was greater in the Fe(II)-EDDS-catalyzed SPC system compared to the Fe(II)-catalyzed SPC system, indicating the effectiveness of adding EDDS as an enhancement factor for the removal of TCE. Moreover, TCE degradation was faster in the HA-Fe(II)-EDDS-catalyzed SPC system compared to the Fe(II)-EDDS-catalyzed SPC system, illustrating that HA can play a synergistic role in TCE degradation. Analysis of iron distribution in the three systems demonstrated that EDDS addition maintained iron in soluble form, and that the generation of soluble ferrous from ferric iron was expedited with addition of HA. Studies using nitrobenzene and carbon tetrachloride probes provided insights on the generation of hydroxyl radical (HO•) and superoxide anion radical (O2•-) in the three systems. A gradual increasing contribution of O2•- to TCE removal in Fe(II)-catalyzed SPC, Fe(II)-EDDS-catalyzed SPC, and HA-Fe(II)-EDDS-catalyzed SPC systems was verified through free-radical scavenger tests. Finally, monitoring of Cl- concentrations manifested the complete dechlorination of TCE. A possible mechanism of TCE degradation involving two pathways of HO• oxidation and O2•- reaction was proposed.