The reaction of Pd(II) with 1,8-dihydroxy-2-(pyrazol-5-ylazo)-naphthalen-3,6-disulphonic acid immobilized by physical sorption onto Dowex 1-X8 ion-exchange resin was investigated with the aim to develop the sorption-spectroscopic test method for the detection of low Pd(II) concentrations in water. The resin phase absorption spectra of the reagent and its Pd(II) complex were followed. The immobilized reagent has the spectral characteristics similar to those in the water and forms with Pd(II) 1:1 complex with the absorption maximum at 650 nm. Parameters, such as pH, wavelength and contact time have been optimized for a given amount of the sorbed reagent. The experimental conditions for the linear dependence of absorbance vs. Pd(II) concentration have been determined.

The real-time textile dyes wastewater contains hazardous and recalcitrant chemicals that are difficult to degrade by conventional methods. Such pollutants, when released without proper treatment into the environment, impact water quality and usage. Hence, the textile dye effluent is considered a severe environmental pollutant. It contains mixed contaminants like dyes, sodium bicarbonate, acetic acid. The physico-chemical treatment of these wastewaters produces a large amount of sludge and costly. Acceptance of technology by the industry mandates that it should be efficient, cost-effective and the treated water is safe for reuse. A sequential anaerobic-aerobic plant-microbe system with acclimatized microorganisms and vetiver plants, was evaluated at a pilot-scale on-site. At the end of the sequential process, decolorization and total aromatic amine (TAA) removal were 78.8% and 69.2% respectively. Analysis of the treated water at various stages using Fourier Transform Infrared (FTIR), High Performance Liquid Chromatography (HPLC)) Gas Chromatography-Mass Spectrometry (GC-MS) Liquid Chromatography-Mass Spectrometry (LC-MS) indicated that the dyes were decolourized and the aromatic amine intermediates formed were degraded to give aliphatic compounds. Scanning Electron Microscope (SEM) and Atomic Force Microscopy (AFM) analysis showed interaction of microbe with the roots of vetiver plants. Toxicity analysis with zebrafish indicated the removal of toxins and teratogens.

The most promising technique for directly converting solar energy into clean fuels and environmental remediation by organic dye degradation is photoelectrochemical (PEC) process. We introduced Sn⁴⁺/Ti⁴⁺ doped α-Fe₂O₃@CuₓO heterojunction photoanode with complete optimization for PEC hydrogen (H₂) generation and organic dye degradation. Improvement of photocurrent photo and reducing overpotentials under optimized conditions lead to enhancing PEC performances, degradation efficiency of organic compounds, and H₂ generation generation rate. The optimized heterojunction photoanode (5TiFe@CuₓO-D) showed IPCE exceeding 42% compared with pristine hematite (Fe₀.₀₁–800₆ₕ) nanostructures (28%). Additionally, all the optimized photoanodes showed higher PEC stability for 10 h. Time-resolved PL spectra confirm the improved average lifetime for heterojunction photoanodes, supporting the enhanced PEC performance. Optimized 5TiFe@CuₓO-D material achieved PEC H₂ generation of ∼300 μL h⁻¹.cm⁻² which is two times higher than pristine hematite’s activity (150 μL h⁻¹.cm⁻²) and almost 99% degradation efficiency within 120 min of irradiation time. Therefore, a state-of-the-art study has been explored for hematite-based heterojunction photoanodes reflecting the superior PEC performance and hydrogen, methyl orange (MO) dye degradation activities. The improved results were reported because of stable morphology and better crystallinity acquired through systematic investigation of thermal effects and hydrothermal duration, improved electrical properties by Sn/Ti doping into the lattice of α-Fe₂O₃ and optimization of CuₓO deposition methods. The formation of well-defined heterojunction minimizes the recombination of the charge carrier and leads to effective transportation of excited electrons for the enhanced PEC performance.

A novel self-assembly method was developed to prepare a γ-Fe₂O₃/graphene oxide (GO) heterogeneous catalyst that showed excellent synergy between photocatalysis and Fenton-like reactions. The γ-Fe₂O₃/GO catalyst prepared on the iron plates demonstrated efficient and reproducible catalytic activities for water treatment. It takes only 80 min to degrade 50 mg L⁻¹ methylene (MB) completely, which is the main non-biodegradable dye in wastewater from the textile industry. The heterogeneous catalyst is stable over a wide range of pH (from 2.0 to 10.2) for MB degradation, and can be easily extracted from solution and repeatedly used with little loss of catalytic activity. The high activity and stability of the catalyst system can be attributed to charge separation between γ-Fe₂O₃ and GO, which could accelerate Fenton-like process and photocatalysis. In addition, the dominant reactive oxidant species responsible for the MB degradation, including the hydroxyl radicals (•OH) and holes (h⁺), were trapped on the surface of the γ-Fe₂O₃/GO composite, as proved by a free-radical quenching experiment. The γ-Fe₂O₃/GO heterogeneous catalyst could potentially provide a solution for removal of non-biodegradable dyes from wastewater in the textile industry.

The effects of arsenic (As), cadmium (Cd) and zinc (Zn) on each other's uptake and oxidative stress in As-hyperaccumulator Pteris vittata were investigated. P. vittata plants were exposed to 50 μM As, Cd and/or Zn for 15 d in 0.2-strength Hoagland solution. When applied alone, P. vittata accumulated 185 mg kg⁻¹ As, 164 mg kg⁻¹ Cd and 327 mg kg⁻¹ Zn in the fronds. While Cd and Zn did not impact each other's uptake, As affected Cd and Zn uptake. Whereas As decreased Zn uptake, Zn affected As speciation in P. vittata fronds, with more arsenate (AsV) than arsenite (AsIII) being present. At 50 μM As, 75 μM Zn increased As accumulation in P. vittata fronds by 10 folds to 2363 mg kg⁻¹ compared to 50 μM Zn. Although AsV was the predominant As species in all tissues, Cd enhanced AsIII levels in the fronds but increased AsV in the roots. Co-exposure of Cd + Zn elevated oxidative stress basing on thiobarbituric acid reactive substances, H₂O₂ content, Evans blue dye uptake, membrane injury index and reactive oxygen species (ROS) relative to single metal. By lowering Cd and Zn concentrations in P. vittata fronds, As reduced the associated stress comparative to Cd or Zn treatment. The results enhance our understanding of the mechanisms underlying the interactions between As, Cd and Zn in As-hyperaccumulator P. vittata.

Biofilm-mediated bioremediation of xenobiotic pollutants is an environmental friendly biological technique. In this study, 36 out of 55 bacterial isolates developed biofilms in glass test tubes containing salt-optimized broth plus 2% glycerol (SOBG). Scanning electron microscopy, Fourier transform infrared (FTIR) spectroscopy, and Congo red- and Calcofluor binding results showed biofilm matrices contain proteins, curli, nanocellulose-rich polysaccharides, nucleic acids, lipids, and peptidoglycans. Several functional groups including –OH, N–H, C–H, CO, COO⁻, –NH₂, PO, C–O, and C–C were also predicted. By sequencing, ten novel biofilm-producing bacteria (BPB) were identified, including Exiguobacterium indicum ES31G, Kurthia gibsonii ES43G, Kluyvera cryocrescens ES45G, Cedecea lapagei ES48G, Enterobacter wuhouensis ES49G, Aeromonas caviae ES50G, Lysinibacillus sphaericus ES51G, Acinetobacter haemolyticus ES52G, Enterobacter soli ES53G, and Comamonas aquatica ES54G. The Direct Red (DR) 28 (a carcinogenic and mutagenic dye used in dyeing and biomedical processes) decolorization process was optimized in selected bacterial isolates. Under optimum conditions (SOBG medium, 75 mg L⁻¹ dye, pH 7, 28 °C, microaerophilic condition and within 72 h of incubation), five of the bacteria tested could decolorize 97.8% ± 0.56–99.7% ± 0.45 of DR 28 dye. Azoreductase and laccase enzymes responsible for biodegradation were produced under the optimum condition. UV–Vis spectral analysis revealed that the azo (−NN−) bond peak at 476 nm had almost disappeared in all of the decolorized samples. FTIR data revealed that the foremost characteristic peaks had either partly or entirely vanished or were malformed or stretched. The chemical oxygen demand decreased by 83.3–91.3% in the decolorized samples, while plant probiotic bacterial growth was indistinguishable in the biodegraded metabolites and the original dye. Furthermore, seed germination (%) was higher in the biodegraded metabolites than the parent dye. Thus, examined BPB could provide potential solutions for the bioremediation of industrial dyes in wastewater.

Chinese cabbage (Brassica rapa ssp. pekinensis) is one of the most popular and frequently consumed leafy vegetables. It was found that atmospheric PM₂.₅-Pb contributes to Pb accumulation in the edible leaves of Chinese cabbage via stomata in North China during haze seasons with high concentrations of fine particulate matter in autumn and winter. However, it is unclear whether both stomata and trichomes co-regulate foliar transfer of PM₂.₅-Pb from atmospheric deposition to the leaf of Chinese cabbage genotypes with trichomes. Field and hydroponic experiments were conducted to investigate the effects of foliar uptake of PM₂.₅-Pb on Pb accumulation in leaves using two genotypes of Chinese cabbage, one without trichomes and one with trichomes. It was verified that open stoma is a prominent pathway of foliar PM₂.₅-Pb transfer in the short-term exposure for 6 h, contributing 74.5% of Pb accumulation in leaves, whereas Pb concentrations in the leaves of with-trichome genotype in the rosette stage were 6.52- and 1.04-fold higher than that of without-trichome genotype in greenhouse and open field, respectively, which suggests that stomata and trichomes co-regulate foliar Pb uptake of from atmospheric PM₂.₅. Moreover, subcellular Pb in the leaves was distributed in the following order of cytoplasm (53.8%) > cell wall (38.5%)> organelle (7.8%), as confirmed through high-resolution secondary ion mass spectrometry (NanoSIMS). The Leadmium™ Green AM dye manifested that Pb in PM₂.₅ entered cellular space of trichomes and accumulated in the basal compartment, enhancing foliar Pb uptake in the edible leaves of cabbage. The results of these experiments are evidence that both stomata and trichomes are important pathways in the regulation of foliar Pb uptake and translocation in Chinese cabbage.

Herein, we report the optimization of nitrogen (N) doping in TiO₂ nanotubes to achieve the enhanced photocatalytic efficiencies in degradation of dye and H₂ gas evolution under solar light exposure. TiO₂ nanotubes have been produced via hydrothermal process and N doping has been tuned by varying the concentration of urea, being the source for N, by solid-state dispersion process. The structural analysis using XRD showed the characteristic occupancy of N into the structure of TiO₂ and the XPS studies showed the existence of Ti–N–Ti network in the N-doped TiO₂ nanotubes. The obtained TEM images showed the formation of 1D tube-like structure of TiO₂. Diffuse reflectance UV–Vis absorption spectra demonstrated that the N-doped TiO₂ nanotubes can efficiently absorb the photons of UV–Vis light of the solar light. The optimized N-doped TiO₂ nanotubes (TiO₂ nanotubes vs urea @ 1:1 ratio) showed the highest degradation efficiency over methyl orange dye (∼91% in 90 min) and showed the highest rate of H₂ evolution (∼19,848 μmol h⁻¹.g⁻¹) under solar light irradiation. Further, the recyclability studies indicated the excellent stability of the photocatalyst for the durable use in both the photocatalytic processes. The observed efficiency was ascribed to the optimized doping of N-atoms into the lattices of TiO₂, which enhanced the optical properties by forming new energy levels of N atoms near the valence band maximum of TiO₂, thereby increased the overall charge separation and recombination resistance in the system. The improved reusability of photocatalyst is attributed to the doping-induced structural stability in N-doped TiO₂. From the observed results, it has been recognized that the established strategy could be promising for synthesizing N-doped TiO₂ nanotubes with favorable structural, optical and photocatalytic properties towards dye degradation and hydrogen production applications.

Water bodies contain a large number of harmful environmental pollutants, including oil, heavy metal ions and dyes, which has become a major global problem. The current work focusses on the development and future prospect of sustainable application of biodegradable cellulose-biomass materials in water treatment, considering that they show an important prospect in wastewater treatment. This paper summarizes the advantages and disadvantages of cellulose-biomass materials in removing harmful substances and pollutants from water and the key problems the technology faces. Cellulose-biomass material has unique structure, is environment friendly, degradable, renewable and provides low energy cost benefits, among other advantages. In this paper, the research progress of wastewater treatment in recent years is reviewed from the following three aspects: oil-water separation, heavy metal ions in water, and dye adsorption. The future research direction is also discussed.

This work demonstrated the development of nanofiber templated metal oxide nanocomposites by hydrothermal and calcination methods for photocatalytic degradation using Congo red (CR) as model pollutant. Herein, we developed PAN/CuO–ZnO nanocomposites by the electrospinning technique followed by heat treatment process i.e hydrothermal and calcination. The obtained nanofibrous composites were characterized by various analytical techniques such as X-Ray Diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Thermogravimetric analysis (TG), High-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), Photoluminescence (PL) and UV–Vis diffuse reflectance spectroscopy (DRS) studies. The results demostrated that the nanocomposites obtained through calcination possess better optical response with robust electronic structures. This is due to the better charge separation of excited electron-hole pairs of p-n heterostructured PAN/CuO–ZnO hybrid nanocomposites. The photocatalytic efficiency is found to be 98% and 93% for nanocomposites obtained through calcination and hydrothermal methods respectively. The reusability studies confirmed the stability and viability of multiple utilizations of photocatalysts. Furthermore, the photocatalytic mechanism corroborated the photocatalytic properties of the integrated facile nanofibrous-metallic (PAN/CuO–ZnO) composites and hence can be implemented in water remediation effectively.