Journal of hazardous materials letters最新文献

The removal of chrome waste (CW) has been identified as a significant environmental problem due to chromium's toxicity. This study tried to make a regenerated flexible sheet (RFS) with a leather alternative effect from chrome waste powder (CWP), cardboard waste fiber (CBWF), and protein binder (PB) fabricated by the hydraulic wet and hot press method. The prepared RFS was characterized by its High-resolution scanning electron microscopy (HR-SEM), thermo gravimetric analysis (TGA), mechanical analysis, and biodegradation properties. The result showed the strong binding achieved with fiber/polymer membrane for RFS. In this regard, RFS with suitable mechanical properties such as tensile strength (37.54 ± 1.32 MPa), elongation at break (33.64 ± 0.52 %), flexibility (5.34 ± 0.67 %), water absorption (27.74 ± 1.56 %), and water desorption (27.46 ± 0.76 %) properties. RFS possessed the required mechanical properties for leather sheet production and it was also biodegradable. The study proves that these composites could be successfully used for the production of cost-effective leather goods and footwear production. Production of useful byproducts from waste is income generating and at the same time reduces environmental pollution and a feasible technology for waste recycling has been proved in this study.

Bisphenol A (BPA), bisphenol F (BPF), and bisphenol S (BPS) are contaminants of emerging concern (CECs) that humans are exposed to. In silico and zebrafish studies have linked BPA, BPF, and BPS exposure to pigmentation abnormalities, but no studies have examined their impact on primary human melanocytes. Herein, we examined the effects of BPA, BPF, and BPS exposure using human epidermal neonatal melanocytes. BPA induced the greatest cytotoxicity, followed by BPS, whereas BPF did not affect viability. BPA did not alter cellular melanin, whereas BPF and BPS diminished it at 100 µM. BPA decreased dendricity, as did BPF and BPS, although BPF was a potent suppressor of dendricity than BPS. BPA inhibited tyrosinase activity, followed by BPF, while BPS weakly suppressed tyrosinase activity. The tyrosinase activity was mostly recovered after the cessation of bisphenol treatments, although it remained lower for BPA and BPF. All bisphenols elevated cellular ROS production, although BPA and BPS showed non-monotonic dose responses. BPA and BPS augmented IL-6 cytokine secretion in melanocyte cultures treated with lipopolysaccharide, but BPF did not, suggesting that they exacerbate melanocyte inflammation. Collectively, these findings indicate BPA, BPF, and BPS, may impair melanocyte function and pose health hazards, warranting more study.

In this proof-of-concept study, a new mass spectrometry-based framework was introduced for concurrent tracking of infectious disease prevalence and community responses. The study focused on the detection of SARS-CoV-2 as the test pathogen and C-reactive protein (CRP) as the representative acute phase response protein. Through mass spectrometry (MS), the research provided preliminary insights into the prevalence of the virus and community acute immune responses, suggesting its strong potential as an early warning system. The high specificity and sensitivity of MS, combined with wastewater-based epidemiology's ability to provide a population-level perspective on virus prevalence, make it a valuable tool for public health surveillance. The study's findings demonstrate the utility of targeted proteomics technology in detecting specific protein biomarkers associated with SARS-CoV-2 infection and inflammation in complex wastewater samples. This approach has advantages over traditional RNA-based methods, including the ability to simultaneously detect acute-phase response proteins such as CRP. The study lays the foundation for future research towards refining analytical techniques to extract more precise data from complex matrices.

Synopsis

WBE proteomics holds a strong potential in wastewater surveillance for pathogens and disease outcomes

Per- and polyfluoroalkyl substances (PFASs) have been found in toilet paper in Europe, the United States, and Africa; however, their presence in Chinese household paper has not been investigated. In this study, 21 legacy and 30 emerging PFASs were analyzed in tissue and toilet paper from China, including 48 samples of different origins and materials. Median concentrations of chlorinated polyfluorinated ether sulfonates (Cl-PFESAs), hexafluoropropylene oxide homologs (HFPOs), and p-perfluorous nonenoxybenzenesulfonate (OBS) were 0.32, 0.19, and 0.10 ng/g dry weight (dw), respectively. The detection frequencies (DFs) of Cl-PFESAs and OBS both were greater than 96%, followed by hexafluoropropylene oxide trimer acid (HFPO-TrA, DF: 85%). Notably, the level of HFPO-TrA in one sample was as high as 540 ng/g dw, indicating a potential environmental risk to humans. In addition, the concentrations of Cl-PFESAs in toilet paper were significantly higher than that in tissue (p < 0.05). However, no significant differences were observed in the concentrations of PFASs in tissue and toilet paper from different materials and origins. This suggests that PFASs, particularly emerging PFASs, are widely detected in tissue and toilet paper products across China, and their presence is a potential source of landfill contamination and human exposure.

Water pollution is a major challenge in the industrial era that gained the attention of researchers, especially for dye wastewater. Membrane technology is applied to address this issue due to its efficient and effective process. MIL-100(Cr) is a metal-organic framework that becomes an interesting material in membrane technology due to its highly porous characteristics (pore sizes of 24 Å and 29 Å), large surface area, and decent stability. In this study, polyvinylidene fluoride (PVDF) was modified with MIL-100(Cr) to fabricate PVDF/MIL-100(Cr) mixed matrix membranes (MMMs) for congo red (CR) dye removal. Furthermore, the membrane performances were determined by its permeability, selectivity, and antifouling properties. The results show that adding MIL-100(Cr) could enhance the membrane’s porosity and average pore size, which led to a boost in membrane permeability. Interestingly, the rejection of the membrane is maintained at a remarkably high level, above 95%, because of the electrostatic repulsion between the membrane surface with anionic congo red. The optimum concentration of MIL-100(Cr) is 1% (w/w), with a permeability of 50.90 L m⁻² h⁻¹ and rejection of 99.9%. Moreover, the flux recovery ratio (FRR) is around 90%, showing notable resistance to the fouling phenomena.

Bioremediation is a promising approach for mitigating commingled contaminations of chlorinated ethenes (CEs) and 1,4-dioxane (DX). However, aerobic bioremediation to simultaneously remove CEs and DX remains challenging. This study aimed to explore the ability of Pseudonocardia sp. D17 (D17) to aerobically degrade CEs and its applicability for concurrent removal of CEs and DX. Aerobic degradation experiments of individual CEs revealed that D17 could degrade trichloroethene (TCE), three isomers of dichloroethene (DCE), and vinyl chloride (VC), and the trend of its degradation ability was cis-1,2-DCE (cDCE) > VC > TCE > trans-1,2-DCE > 1,1-DCE. Notably, the CE-degrading activity of D17 was expressed even without any auxiliary substrates. Further, when TCE, cDCE, or VC was co-present with DX (each at 1 mg/L), D17 could degrade both compounds without any significant inhibition (for TCE and cDCE) or with only a transient and reversible suspension of its DX degradation ability (for VC). These findings indicated that D17 is a promising agent for the aerobic bioremediation of CEs and DX co-contamination and provide novel insights into the future development of efficient aerobic bioremediation strategies.

The widespread and injudicious usage of antibiotics to contain pathogenic microbial infections, coupled with inadequate treatment of wastes containing non-metabolized antibiotics and their residues is resulting in rising environmental antibiotic concentrations, leading to ‘antibiotic pollution’. Antibiotic pollution is an emerging global challenge as it is proving a major driver for antibiotic- or antimicrobial-resistance (ABR/ AMR) with escalating ramifications worldwide, precipitating a surge in human morbidity. The extensive administration of antibiotics across domains such as human healthcare settings, agriculture, and aquaculture farming endangers the presence of antibiotics in diverse matrices including water, soil, and air. As a result, this dissemination significantly leads to the development of antibiotic resistance in the profuse sectors of the environment further provoking consequential health implications at different trophic levels. Owing to its significance, and to mitigate antibiotic pollution and its subsequential AMR, governmental guidelines and regulations are implemented across the globe to cultivate public awareness as concerted efforts for addressing this global predicament. Given the insufficient attention to the growing antibiotic pollution issues, prompt efforts must be taken to contemplate current circumstances and the rigor of the ongoing research. In this review, we endeavor to elucidate the escalation of antibiotic concentration and antibiotic-driven AMR in water, air, and soil environments with potential public health threats. Further, it focuses on various strategies and interventions to attenuate antibiotic pollution and mitigate its adverse impacts on the healthcare infrastructure, highlighting the success stories, challenges, and future directions.

Sugars and sugar-rich agricultural by-products are cheaper and eco-friendly alternatives to conventional reductants used in recovering metals from spent lithium-ion batteries. Still, they are rarely used due to a poor understanding of their performance and reaction chemistry. In this study, two hypotheses bearing on the role of chemistry and influence of non-sugary organic compounds (impurities) on the performance of sugars, namely: glucose, fructose and sucrose, and a parent sugar-rich agro-industrial by-product – molasses, as reductants in the leaching of Li, Co, Mn and Ni from spent lithium-ion battery cathode material were tested. Statistical analysis using ANOVA revealed that the performance of the sugars and molasses are similar with >85% Mn, >88% Ni, >88%Co and >98% Li leached at 90 °C and 60 min. This shows that the presence of non-sugar organic compounds does not hamper the performance of the sugars-based reductants. The performance of the sugars relies more on temperature than chemistry. Furthermore, evaluation of the oxidation pathway hints at a potential inhibition of secondary oxidation reactions at lower temperatures. This study provides statistically validated proof that the performance of sugarcane molasses, even at lower concentration, is equipollent to the pure sugars in the leaching of critical metals from spent lithium-ion batteries.

The development of adsorbents capable of adsorbing both anionic and cationic dyes in wastewater treatment remains a challenge. This study presents the successful fabrication of Nb₂O₅-MgAl layered double hydroxide (LDH) nanocomposites for the effective removal of methylene blue (MB) and Congo red (CR) dyes via a one-step hydrothermal method. Incorporating a small amount of Nb into MgAl-LDH proved to be an effective strategy for creating nanocomposite materials with dual characteristics. The material’s morphological and crystalline structures were confirmed using FESEM-EDS and XRD. Incorporating Nb during the material preparation led to a remarkable enhancement in the material’s adsorption capacity - up to 3.4-fold and 9.0-fold increases for CR and MB, respectively. The kinetic and point zero charge analysis confirmed that the adsorption of the dyes onto the adsorbent surfaces occurred via an ionic interaction mechanism. These findings offer a promising alternative for fabricating dual-functional adsorbents, enhancing the effectiveness of dye removal in wastewater treatment technologies.

To assess the performance of hazardous waste sites remediation technologies like in situ chemical oxidation (ISCO) with persulfate (S₂O₈²⁻) researchers must periodically measure concentrations of target contaminants. Due to the presence of relatively high concentrations of the residual oxidant expected in many samples, the standard analytical method requires the addition of a relatively high concentration of ascorbic acid to prevent the oxidation process from continuing after sample collection. We discovered that addition of ascorbic acid quencher results in a radical chain reaction that transforms two common halogenated solvents (i.e., tetrachloroethene and hexachloroethane). To avoid the artifact associated with the radical chain reaction, a small quantity of n-hexane can be added to aqueous samples to extract target compounds and protect them from the radical chain reaction initiated by addition of the quencher. We recommend the use of this alternative sample preservation method whenever high concentrations of residual S₂O₈²⁻ are expected to be present in water samples that are contaminated with halogenated solvents.