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.

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.

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.

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.

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.

For effective photocatalytic pollutant degradation on bismuth tungstate (Bi₂WO₆), it is vital to enhance the photogenerated charge separation and the photochemical stability. Herein, we successfully fabricated yttrium (Y)-Bi₂WO₆/graphene (G) nanocomposites with a significantly enhanced visible light–driven photocatalytic ability to degrade Rhodamine B compared with the bare Bi₂WO₆. This is attributed to the remarkably improved visible light absorption capability and photogenerated charge separation after doping yttrium and subsequent coupling with graphene, as revealed by photoluminescence and electrochemical impedance spectroscopies. Moreover, trapping experiments were carried out to clarify that photogenerated ·O²⁻ and holes were the dominant oxidative species in the photocatalytic reaction. In addition, it was confirmed that the resulting composites maintained good photostability and chemical stability during recycling tests. Graphical abstract

The use of engineered nanomaterials (ENMs) increases concerns relating to their fate, behavior, and toxicity due to their increased exposure to the environment. These ENMs end up in wastewater treatment plants (WWTPs), and the bacteria in these systems are sensitive to compounds such as heavy metals, which reduces the functionality of the WWTP. In this work, the fate and behavior of Bi₂O₃-BiVO₄ in a WWTP using the OECD 303A guideline was studied. The Bi₂O₃-BiVO₄ NPs were synthesized through a hydrothermal and impregnation method. X-ray diffraction showed monoclinic phases of both Bi₂O₃ and BiVO₄ NPs. The effect of Bi₂O₃-BiVO₄ NPs was monitored using chemical oxygen demand (COD) and 5-day biological oxygen demand (BOD₅). The COD and BOD₅ for the sludge retention time where the NPs were added was > 70%. This showed that the NPs had no effect on the functionality of the treatment processes as it was further affirmed by the TPC measurements. Inductively coupled plasma–optical emission spectroscopy (ICP-OES) showed that the fate of the NPs was through the activated sludge than the effluent, whereby 90% of Bi and V were absorbed in the activated sludge and 10% in the effluent. The results indicate that the NPs have the potential to permeate through the environment segments through the wastewater sludge compared to the effluent. XRD analysis of the test sludge showed that the crystal phases of the heterojunction remained unchanged, and this could ascertain that the treatment conditions did not transform the NPs into toxic forms.

As the use of dangerous substances in consumer products increases, these substances may also be found in society’s end products, among them sewage sludge. Measuring concentrations in sewage sludge can be a way to reflect the consumption of a substance. By using substance flow analysis, the inflow, stock and outflow of the specific substance to, e.g. a city region, may be analysed. Bismuth is a heavy metal that is found in increasing levels in sewage sludge in Swedish wastewater treatment plants (WWTPs) and a similar increase cannot be excluded for WWTPs around the world. This study aims to examine possible sources that could explain the amounts measured in one Swedish WWTP. Household products such as cosmetics (24 %) and plastics (14 %) are found to be major sources of Bi measured in sewage sludge. The remaining unidentified amounts in this study (approximately 50 %) are most likely found in effluent waters from industries or sources outside the household. There is, however, no information on measurements of Bi released by industry available and there is no legislation in place that may encourage industry to conduct such measurements.

The present work focused on treatment of eosin (EO) by photocatalysis (PC) combined with electrocatalysis (EC) process. Bismuth oxychloride/titanium dioxide (BiOCl/TiO₂) hybrid particles, which were used as new heterogeneous photocatalysts, were exploited in a reverse microemulsion approach and were characterized by XRD, UV–Vis diffuse spectra, BET, and SEM technologies. All degradation experiments were performed using a self-assemble experimental setup, in which PC and EC could be carried out simultaneously or individually. The results indicated that BiOCl/TiO₂ showed enhanced photocatalytic performance under UV irradiation, and 50% BiOCl/TiO₂ exhibited the best photoactivity due to its high degree of crystallization, the mesoporous structure and corresponding large special surface area, improved absorption ability in UV region, and the heterojunction formed between two coupling particles. The combined degradation process displayed synergistic effect on the degradation of EO owing to the generation of H₂O₂ at graphite cathode. The parameters such as, pH, reaction current, and initial concentration of EO were monitored in order to optimize the operating conditions. Pseudo-first-order kinetics was proposed and roughly fitted the combined degradation of EO. The combined system in this work suggested a new research idea for the degradation of dye wastewater.