The adsorption of radioactive iodine, which is capable of presenting high mobility in aquatic ecosystems and generating undesirable health effects in humans (e.g., thyroid gland dysfunction), was comprehensively examined using pristine spent coffee ground biochar (SCGB) and bismuth-impregnated spent coffee ground biochar (Bi@SCGB) to provide valuable insights into the variations in the adsorption capacity and mechanisms after pretreatment with Bi(NO₃)₃. The greater adsorption of radioactive iodine toward Bi@SCGB (adsorption capacity (Qₑ) = 253.71 μg/g) compared to that for SCGB (Qₑ = 23.32 μg/g) and its reduced adsorption capability at higher pH values provide evidence that the adsorption of radioactive iodine with SCGB and Bi@SCGB is strongly influenced by the presence of bismuth materials and the electrostatic repulsion between their negatively charged surfaces and negatively charged radioactive iodine (IO₃⁻). The calculated R² values for the adsorption kinetics and isotherms support that chemisorption plays a crucial role in the adsorption of radioactive iodine by SCGB and Bi@SCGB in aqueous phases. The adsorption of radioactive iodine onto SCGB was linearly correlated with the contact time (h¹/²), and the diffusion of intra-particle predominantly determined the adsorption rate of radioactive iodine onto Bi@SCGB (Cₛₜₐgₑ II (129.20) > Cₛₜₐgₑ I (42.33)). Thermodynamic studies revealed that the adsorption of radioactive iodine toward SCGB (ΔG° = −8.47 to −7.83 kJ/mol; ΔH° = −13.93 kJ/mol) occurred exothermically and that for Bi@SCGB (ΔG° = −15.90 to −13.89 kJ/mol; ΔH° = 5.88 kJ/mol) proceeded endothermically and spontaneously. The X-ray photoelectron spectroscopy (XPS) analysis of SCGB and Bi@SCGB before and after the adsorption of radioactive iodine suggest the conclusion that the change in the primary adsorption mechanism from electrostatic attraction to surface precipitation upon the impregnation of bismuth materials on the surfaces of spent coffee ground biochars is beneficial for the adsorption of radioactive iodine in aqueous phases.

Most studies of metals exposure focus on the heavy metals. There are many other metals (the transition, alkali and alkaline earth metals in particular) in common use in electronics, defense industries, emitted via combustion and which are naturally present in the environment, that have received limited attention in terms of human exposure. We analysed samples of whole blood (172), urine (173) and drinking water (172) for antimony, beryllium, bismuth, cesium, gallium, rubidium, silver, strontium, thallium, thorium and vanadium using ICPMS. In general most metals concentrations were low and below the analytical limit of detection with some high concentrations observed. Few factors examined in regression models were shown to influence biological metals concentrations and explained little of the variation. Further study is required to establish the source of metals exposures at the high end of the ranges of concentrations measured and the potential for any adverse health impacts in children.

Bismuth is a heavy metal whose biogeochemical behaviour in the marine environment is poorly defined. In this study, we exposed three different species of macroalga (the chlorophyte, Ulva lactuca, the phaeophyte, Fucus vesiculosus, and the rhodophyte, Chondrus crispus) to different concentrations of Bi (up to 50 μg L⁻¹) under controlled, laboratory conditions. After a period of 48-h, the phytotoxicity of Bi was measured in terms of chlorophyll fluorescence quenching, and adsorption and internalisation of Bi determined by ICP after EDTA extraction and acid digestion, respectively. For all algae, both the internalisation and total accumulation of Bi were proportional to the concentration of aqueous metal. Total accumulation followed the order: F. vesiculosus > C. crispus > U. lactuca; with respective accumulation factors of about 4200, 1700 and 600 L kg⁻¹. Greatest internalisation (about 33% of total accumulated Bi) was exhibited by C. crispus, the only macroalga to display a phytotoxic response in the exposures. A comparison of the present results with those reported in the literature suggests that Bi accumulation by macroalgae is significantly lower than its accumulation by marine plankton (volume concentration factors of 10⁵ to 10⁷), and that the phytotoxicity of Bi is low relative to other heavy metals like Ag and Tl.

We investigated the influence of the intertidal geothermal hot spring (GHS) on the biogeochemistry of trace elements in Santispac Bight, Bahía Concepción (Gulf of California). The geothermal fluids were enriched in As and Hg mainly in ionic form. The suspended particulate matter of the GHS had elevated enrichment factor (EF) >1 of As, Bi, Cd, Co, Cu, Mn, Mo, Sb, Sn, Sr, Ti, U and Zn. The sediment core from GHS1 had high concentration of As, Hg, Corg, S, V, Mo, and U and the extremely high EF of these elements at 8cm of the core. The maximum bioaccumulation of As and Hg was in seaweeds Sargassum sinicola collected near the GHS2. The results confirm the input of trace elements to the coastal zone in Bahía Concepción from geothermal fluids and the evident modification of the chemical composition of the adjacent marine environment.

Body distribution and growth- and nutritional status-dependent accumulation of 21 trace elements were investigated in harbor seals (Phoca vitulina) stranded in the North Sea coast in 2002. Higher concentrations and burdens of Mn, Se, Mo, Ag, Sn, Hg, and Bi in the liver, Cd in the kidney, As in the blubber, and Co, Sr, and Ba in the bone were observed. Significant positive correlations of hepatic Se, Mo, Ag, Cd, Sn, Hg, Tl, and Bi with standard body length were found, while significant negative relationships were detected for Mn, As, Rb, Sr, and Sb in the liver. Concentrations of Co, Se, Sr, Sn, Hg, and Bi in the liver, V, Sr, Ag, Sn, and Hg in the kidney, V, Mn, Co, Rb, Sr, Sn, Ba, and Pb in the blubber increased with decreasing blubber thickness of harbor seals, indicating enrichment of these elements in the target tissue by emaciation.

Bismuth molybdate (Bi₂MoO₆) nanostructures has attracted many researches as an advanced photocalysts for the organic contaminants. In this paper, bismuth molybdate Bi₂MoO₆ nanoparticles were synthesized using a simple hydrothermal method at varied pH (2, 4, 6, 8, and 10) for 15 h at 180 °C. The results reveal the variation pH precursor solutions have a significant impact on the morphology, phase formations, and photocatalytic activity of samples. The synthesized samples at low pH level were characterized by FESEM analysis revealing Bi₂MoO₆ nanoplates have formed while gradually convert to Bi₂MoO₆ spherical nanoparticle at high PH level as shown in energy dispersive X-ray spectroscopy (DES) peaks. The X-ray diffraction patterns reveal characteristic peaks corresponding to mixed phases of Bi₂MoO₆ and cubic Bi₄MoO₉ at high pH value. The optical absorption study exhibit Bi₂MoO₆ nanoplates absorbed visible light with blue shift when compared to the cubic Bi₄MoO₉ structures. Moreover, the photocatalytic activity results revealed that nanoplates in pH = 4 sample has excellent photocatalytic activity for degradation of rhodamine (RhB), methylene orange (MO), and phenol under visible-light irradiation (λ > 400 nm) as well as exhibit the photodegradation 90% of phenol within 300 min.

Visible light active 1D/2D-NiMoO₄/BiOI nanocomposite photocatalyst has been constructed by single step solvothermal method. Various compositions of NiMoO₄/BiOI nanocomposites are prepared by loading different amounts of nickel molybdate (NiMoO₄) (1, 2, 3 wt%) to the bismuth oxy iodide (BiOI) and investigated by XRD, FTIR, SEM, EDAX, TEM, UV–vis DRS, and PL analysis. Among the as-prepared photocatalysts, 1 wt% NiMoO₄ incorporated BiOI (NMBI-1) showed superior photocatalytic activity with a rate constant of 0.0442 min⁻¹ for methylene blue degradation. While the bandgap values of pure BiOI and NiMoO₄ are 1.94 and 2.43 eV, respectively, the optimized NMBI-1 exhibited a lower bandgap energy of 1.64 eV, and showed about 2 and 3.7 times higher photodegradation ability than the pure NiMoO₄ and BiOI, respectively, towards MB removal under visible light. The NMBI-1 nanocomposite photocatalyst is stable even after four cycles, indicating an excellent photostability and recyclability. Charge carriers on the interface of NiMoO₄ and BiOI easily transferred via the newly formed heterojunction, thereby increasing the photocatalytic performance. Photochemically formed h⁺ and.OH are found to be the major species in the MB removal under visible light illumination. Therefore, the 1D/2D-NiMoO₄/BiOI nanocomposite photocatalyst materials may be considered for the wastewater remediation processes.

The conversion of CO₂ into new carbon-based products, such as fuels and chemicals, is an attractive and promising means of mitigating global energy needs and minimizing environmental damage. Although bismuth tungstate (Bi₂WO₆) as a photocatalyst can promote CO₂ photoreduction, a systematic study for the development of a low-cost and efficient catalyst is needed. Thus, Bi₂WO₆ with different morphologies was successfully synthesized using the hydrothermal method. An experimental design was applied to investigate the effect of synthesis time and PVP (polyvinylpyrrolidone) concentration on catalyst photocatalytic activity. Crystal structures, morphologies, optical absorption, and surface charges of the catalysts were characterized by X-ray diffraction, scanning electron microscope, UV–vis diffuse-reflection spectroscopy, nitrogen adsorption, and zeta potential. All samples exhibited good performance for the photoreduction of CO₂ into ethanol, and both time and PVP concentration were significant in the ethanol yield. Changes in synthesis conditions induced differences in catalyst characteristics, such as morphology, crystallinity, and, predominantly, surface area. Furthermore, PVP addition improved photocatalytic efficiency by up to 258% compared with results without the surfactant. The best sample, W-8h-10%, presented a flower-like morphology and ethanol yield of 68.9 μmol g⁻¹ h⁻¹.

Bismuth vanadate (BiVO₄) nanostructured films were prepared and successfully applied for peroxymonosulfate (PMS) activation for the degradation of rhodamine B (RhB) in aqueous solution. The BiVO₄ thin films were obtained by thermal reaction between electrodeposited bismuth (Bi) films and vanadium precursor. The as-prepared BiVO₄ porous, nanoflowers, and cluster nanostructures were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Raman spectroscopy, and BET analysis. The catalytic performance of BiVO₄ nanostructures has been carefully evaluated in activating PMS for the degradation of RhB. The nanoflower-like BiVO₄ nanostructures exhibit the best catalytic activity. Under optimized conditions, the complete catalytic degradation of RhB using BiVO₄ nanoflowers/PMS system was achieved in 17 min at room temperature as revealed by high-performance liquid chromatography (HPLC) analysis. Quenching experiments suggested that sulfate radicals are the main active species in the degradation process. Additionally, BiVO₄ catalyst remained stable without any apparent activity loss after five cycling runs.

CuₓO/Bi₂O₃ oxides grown on nickel foam were synthesized via an electrodeposition method to degrade indoor HCHO under visible light irradiation and fully characterized by XRD, SEM, FT-IR, and UV-Vis technologies. The characterization results showed that the CuₓO/Bi₂O₃ oxides were successfully loaded on nickel foam and the visible light response spectrum was expanded to 740 nm. Plackett–Burman design combined with central composite design has been used to optimize factors that affect HCHO removal performance. The results demonstrated that bismuth nitrate content, polyethylene glycol 600 content, sintering time, and lactic acid concentration were the four most important factors affecting the HCHO removal performance over CuₓO/Bi₂O₃ sample. The optimum CuₓO/Bi₂O₃ sample could degrade 88.796% of HCHO in 300 min at the conditions of 4.28 mol/L lactic acid, 4.86% polyethylene glycol 600, 194.03 min sintering time, and 45.83 g bismuth nitrate, and the HCHO removal rate remained 82.3% after five cycles. A plausible mechanism for the degradation of HCHO under visible light irradiation was proposed. This work provides a feasible solution for removing indoor formaldehyde in the field of photocatalysis.