Search Results (9,420)

The CO₂ absorption rate and total uptake by MgO aqueous suspensions were investigated in batch experiments by systematically varying MgO concentrations (0.5–5 wt.%), CO₂ flow rates (0.5–2 L/min), temperatures (278–363 K), NaCl salinities (0–7 wt.%), Na₂SO₄ and K₂SO₄ concentrations (0–10.5 wt.%), and gas–liquid mixing systems (pipe outlet and porous stone sparger). Results show that temperature strongly controls the carbonation process: increasing temperature above 303 K consistently reduced both the CO₂ absorption rate and the total CO₂ uptake due to the destabilization of metastable Mg(HCO₃)₂ solutions and accelerated precipitation of less soluble hydrated magnesium carbonates. Under optimal low-temperature conditions (278–283 K, 1–1.5 wt.% MgO, sparger mixing, pure system), the average capture efficiency reached ≈ 35%, with maximum peaks over 70% and total CO₂ uptakes of ≈ 12–17 L. Adding NaCl at typical seawater levels (3.5–7 wt.%) slightly increased CO₂ uptake at temperatures above 323 K. Sulfate ions (Na₂SO₄ and K₂SO₄) were found to enhance the absorption rate at low concentrations (<2 wt.%) but reduce it at higher levels, with no significant impact on the total CO₂ uptake observed in this study. Using a CO₂ sparger significantly improved gas–liquid contact, achieving average CO₂ capture efficiencies above 70% at low temperatures, compared to <20% with simple pipe bubbling. A direct comparison with Ca(OH)₂ aqueous carbonation confirmed that, despite its lower solubility and slower kinetics, MgO can outperform Ca-based systems under specific conditions. These results provide practical experimental benchmarks and process guidance for designing Mg-based aqueous carbonation systems, including applications that use brines, industrial wastewater or seawater. Full article

Karst aquifers, vital freshwater resources, are highly vulnerable to agricultural pollution, yet their hydro-geochemical responses remain poorly understood due to high spatial heterogeneity. This study aimed to unravel these complex responses in a subtropical karst agricultural catchment to provide a basis for its sustainable management. We employed high-frequency monitoring at a headwater spring (background), a depression well (hotspot), and the catchment outlet (integrated) in Southwest China. Using hydrological and geochemical data from 2017, we applied Principal Component Analysis (PCA) to apportion natural and anthropogenic sources. The main findings revealed significant spatial heterogeneity, with the depression well acting as a contamination hotspot characterized by rapid hydrological responses and elevated SO₄²⁻ and Cl⁻ concentrations. PCA successfully decoupled an “anthropogenic factor” (PC1, 40.5%) from a “natural weathering factor” (PC2, 25.2%). Critically, agricultural SO₄²⁻ at the hotspot was counter-intuitively higher during the wet season than the dry season, opposing the typical dilution pattern of background ions and revealing that depressions act as contaminant-concentrating pathways, whose risks are severely underestimated by traditional outlet monitoring. The anomalous sulfate dynamics reveal a cross-seasonal “storage-and-release” mechanism (legacy effect) within the karst Critical Zone, demonstrating that these systems can buffer and “remember” contaminants. Full article

In the saline, cold, and arid regions of Western China, the adhesive performance at the carbon fiber-reinforced polymer (CFRP)–concrete interface critically affects the long-term reliability of CFRP-strengthened structures. Replacing the organic epoxy resin (EP) with inorganic magnesium phosphate cement (MPC) has been proposed as an alternative. However, comparative studies on the deterioration of MPC- and EP-bonded CFRP–concrete under sulfate freeze–thaw cycles are limited. This study employed double-shear tests to systematically compare the failure modes, ductility, and bond performance of the CFRP–concrete interface bonded with MPC and EP after 25, 50, and 75 sulfate freeze–thaw cycles. The results indicate that, as the number of cycles increased, MPC-bonded specimens exhibited progressive interfacial peeling, whereas EP-bonded specimens underwent abrupt brittle fracture. At 0, 25, 50, and 75 cycles, the peak strains of MPC specimens exceeded those of EP specimens by 9.28%, 10.13%, 5.99%, and 0.86%, respectively, indicating greater ductility. Bond performance declined markedly for both groups as cycles increased, with MPC specimens showing greater deterioration. After 75 cycles, compared with EP-bonded specimens, MPC-bonded specimens showed a 16.56% lower interfacial load capacity, a 21.53% reduction in peak bond stress, and a 6.03% shorter effective bond length. This systematic comparison of MPC- and EP-bonded CFRP–concrete under sulfate freeze–thaw exposure provides guidance for adhesive selection and strengthening practices in saline, cold, and arid regions. Full article

The ever-increasing number of discarded end-of-life dialysate polyamide thin-film composite membranes (DEoLMs) from presents both environmental and economic challenges for health centers. Traditional thermo-chemical cleaning techniques have been deployed for the rehabilitation of DEoLMs. This study further investigated the application of chemo-ultrasonication rehabilitation of dialysate-production-related DEoLM for potential reuse in spent dialysate recovery considering salt and creatinine—a typical uremic toxin-removal from water. The DEoLM was rehabilitated using low-concentration citric acid (CA) and sodium lauryl sulfate (SLS) under ultrasonic waves (45 kHz, 30 min agitation). Considering different rehabilitation protocols, the synergistic effects of heating (HT) and the chemical agents, with and without and ultrasonic waves (SC) were evaluated through FTIR, SEM, and EDX analyses, and the performance of the rehabilitated DEoLM was assessed via water flux and permeance, and efficiencies for conductivity and creatinine rejection. The fully integrated protocol chemo-ultrasonication (HT + SC + chemical agents) yielded the highest performance, achieving 93.56% conductivity and 96.83% creatinine removal, with water flux of 113.48 L m⁻² h⁻¹ and permeances of 6.31 L m⁻² h⁻¹ bar⁻¹, at markedly reduced pressures. The chemo-sonic-rehabilitated-DEoLM removed the organic–inorganic foulants beyond thermo-chemical cleaning. This suggests that the sonication waves had a great impact regarding rejuvenating the fouled DEoL dialysate membrane, offering a sustainable, cost-effective pathway for extending membrane life, and supporting sustainable water management to achieve circular economy goals within healthcare centers. Full article

Examining the changing patterns and underlying mechanisms of soil biomass carbon stocks constitutes a fundamental aspect of soil biology. Despite the potential influence of the sulfur cycle and the life strategies of organisms on community biomass, these factors have rarely been studied in tandem. Biocrusts are model systems for studying soil ecosystems. In this study, metagenomic analysis of biocrusts related to different life strategies from five batches over four consecutive years demonstrated that, in free-living communities, microbial biomass carbon (MBC) synthesis, via assimilatory sulfate reduction (ASR), is primarily coupled with the 3-hydroxypropionate/4-hydroxybutyrate and Calvin–Benson–Bassham cycles. These pathways are affected by the oxidation-reduction potential (Eh), pH, electrical conductivity, and nutrient levels. The decomposition of organic carbon (OC) via dissimilatory sulfate reduction (DSR) was accompanied by the production of dimethyl sulfide (DMS), which was influenced by the C/S ratio and moisture, whereas the synthesis of MBC by symbiotic communities was found to be affected by Eh and pH, and decomposition was affected by the C/S ratio. The MBC stock was influenced by all strategies, with resource strategies having the greatest impacts during the growing season, and the contribution of chemotrophic energy was most significant in free-living communities. In conclusion, the MBC in biocrusts is associated with both ASR and DSR and is facilitated by the A-, S-, and P-strategies under the regulation of the stoichiometric C/S ratio. The exploration of microbial life strategies and sulfur cycling in biocrusts within arid ecosystems in this study offers a new perspective on the patterns of change in soil biomass carbon stocks. Full article

With the rapid development of infrastructure and the need to protect natural ecosystems, manufactured sand is used to replace river sand in concretes. To compare the deterioration patterns of concretes made with different sands, C50 specimens using basalt (C50X), tuff (C50N), and granite (C50H) manufactured sands and river sand (C50T) were prepared, then tested outdoors by full burial in a sulfate saline soil and indoors by accelerated freeze–thaw in a sulfate solution. The outdoor experiments indicate that C50X deteriorated the slowest, whereas the resistance to mass loss ranking was: C50X > C50H > C50N > C50T. In the indoor freeze–thaw experiments, C50X also performed best, retaining 51% relative dynamic modulus of elasticity (RDME) after 450 cycles. X-ray diffraction and scanning electron microscopy showed that C50T was weakened by abundant MgSO₄·7H₂O crystals, while C50X formed a denser matrix that limits salt-crystallization expansion. Moreover, a GM(1,1)-Markov model was developed to forecast long-term durability. For C50X, the model predicted an estimated service life of 68 months in the outdoor environment, at which point it is projected to reach the 5% mass loss failure threshold. Separately, it forecasted that the RDME would remain above 41% after 450 indoor freeze–thaw cycles. Full article

Heparan sulfate proteoglycans (HSPGs) are essential constituents of the extracellular matrix (ECM) and cell surface, orchestrating a wide range of biological processes, such as cell adhesion, migration, proliferation, and intercellular communication. Through their highly sulfated glycosaminoglycan chains, HSPGs serve as crucial modulators of bioavailability and signaling of growth factors, cytokines, and chemokines, thereby influencing tissue homeostasis. Their dynamic remodeling is mediated by numerous enzymes, with heparanase (HPSE) playing a predominant role as the only known human endo-β-D-glucuronidase that specifically cleaves heparan sulfate chains. Beyond its well-documented enzymatic activity in ECM degradation and the release of HS-bound molecules, HPSE also exerts non-enzymatic functions that regulate intracellular signaling cascades, transcriptional programs, and immune cell behavior. Dysregulated HPSE expression or activity has been implicated in various pathological conditions, including fibrosis, chronic inflammation, cancer progression, angiogenesis, metastasis, and immune evasion, positioning this enzyme as a pivotal driver of ECM plasticity in both health and disease. This review provides an updated overview of HSPG biosynthesis, structure, localization, and functional roles, emphasizing the activity of HPSE and its impact on tissue remodeling and disease pathogenesis. We further explored its involvement in the hallmark processes of cancer, the inflammatory tumor microenvironment, and its contribution to fibrosis. Finally, we summarize current therapeutic strategies targeting HPSE, outlining their potential to restore ECM homeostasis and counteract HPSE-driven pathological mechanisms. A deeper understanding of the HSPG/HPSE axis may pave the way for innovative therapeutic interventions in cancer, inflammatory disorders, and fibrotic diseases. Full article

Major vibrational spectroscopy studies have focused on the preparation of chromium coatings via chemical processes (conversion coatings), and few studies have focused on electrochemical processes (electrodeposition). Initially, the chemical precursors were hexavalent chromium salts, but these compounds are now replaced by less toxic trivalent ions. There is a profound understanding of the process when vibrational spectroscopy is used in combination with other techniques. This is the case for chromium(VI) conversion coatings, and the results of several techniques, such as synchrotron infrared microspectroscopy, have made it possible to understand the structure of the two-layer coating and the chemical composition of each layer. Vibrational spectroscopy confirmed the mechanism for coating formation, in which ferricyanide was a redox mediator. In addition, vibrational spectroscopy was effective in determining the mechanism of corrosion resistance of the coatings. Conversely, there are very few studies on the electrodeposition of trivalent chromium ions, and the mechanics of electrodeposition are unknown. To simplify the use of spectroscopy, spectra of potassium dichromate and chromium(III) sulfate are presented as references for coating studies, and a compilation of $\mathrm{C}\mathrm{r}\left(\mathrm{I}\mathrm{I}\mathrm{I}\right)-\mathrm{O}$ and $\mathrm{C}\mathrm{r}\left(\mathrm{V}\mathrm{I}\right)-\mathrm{O}$ vibrational modes is provided to facilitate band assignment. Our review highlights that spectroscopic techniques have been insufficiently applied in this field; however, the results of vibrational spectroscopy accelerate the transition to safer Cr(III) technology. Full article

The Evevpenta gold–silver epithermal deposit, belonging to an adularia–sericite or low-sulfidation type, is in the northern part of the Kamchatka Peninsula within the Oligocene–Quaternary Central Kamchatka volcanic belt. Variously native gold, silver, and Au–Ag chalcogenides, including calaverite, petzite, hessite, acanthite, uytenbogaardtite-petrovskaite, and naumannite, constitute its Au–Ag mineralization. Extensive fluid inclusion studies, involving fluid inclusion petrography, Raman spectroscopy, and microthermometry, revealed that quartz from gold-bearing adularia–quartz veins crystallized from low-salinity fluids (T ice melting from −0.1 to −3.3 °C) at moderate to low temperatures (140 to 364 °C). The mineralizing fluids consisted of Na, K, and Mg sulfate and bicarbonate-bearing aqueous solutions and low-density CO₂. The gold-bearing mineral assemblages were formed within narrower temperature ranges. The gold–telluride–quartz assemblage was deposited between 325 and 175 °C, while the telluride–sulfide–quartz formed between 219 and 258 °C. Possible influx of meteoric waters led to progressive cooling and a decrease in salinity from the early to late fluid generations during mineral deposition. Overall data on ore and associated with metasomatic alteration mineralogy indicate that the ore formation occurred under relatively reduced or neutral conditions from weakly acidic to near-neutral aqueous solutions, possessing relatively high sulfur and tellurium fugacity. Full article

In this study, 101 and 102 rainwater samples were collected from April 2020 to February 2024 in a coastal and marine area, respectively. The results show that the Cl/Na ratios in both study areas were lower than the seawater value (1.17), suggesting chloride depletion. The chloride depletion rates in both areas decreased after the COVID-19 lockdown period. The molar ratio of NH₄⁺ to non-sea-salt sulfate (nss-SO₄²⁻) was 1.54, with a mixture of (NH₄)₂SO₄ and NH₄HSO₄ in the coastal area, and 0.83, with NH₄HSO₄ as the main form, in the marine area. A decreasing trend attributed to high O₃ and relative humidity (RH) levels occurred in 2022. Among the dissolved organic nitrogen (DON) species, DON accounted for 24% and 32% of the total dissolved nitrogen (TDN) in the coastal and marine areas, respectively, indicating a greater relative contribution under lower anthropogenic influence. On the basis of the correlation between the species and source analysis results, NO₃⁻ mainly originated from fossil fuel combustion, NH₄⁺ originated from agricultural emissions and secondary aerosols, and DON originated from secondary aerosols via combustion processes and natural emissions. In terms of the flux, due to lockdown activities, the Dissolved Inorganic Nitrogen (DIN) flux decreased significantly from 40.6 to 19.3 mmol m⁻² yr⁻¹ in the coastal area and from 27.7 to 15.1 mmol m⁻² yr⁻¹ in the marine area. Additionally, a slight decrease occurred in the DON flux, from 21.6 to 19.3 mmol m⁻² yr⁻¹ and from 27.7 to 15.1 mmol m⁻² yr⁻¹, respectively. Regarding new production, based on nitrogen input, the level in the coastal area decreased from 5.83 to 2.10 g C m⁻² yr⁻¹, and that in the marine area decreased from 3.92 to 1.55 g C m⁻² yr⁻¹, indicating a significant reduction during the COVID-19 lockdown. Full article

Background: Alzheimer’s disease (AD) is a progressive neurodegenerative disorder with unclear pathogenic mechanisms. Dysregulated zinc metabolism contributes to AD pathology. This study aimed to identify zinc metabolism-related hub genes to provide potential biomarkers and therapeutic targets for AD. Methods: We performed an integrative analysis of multiple transcriptomic datasets from AD patients and normal controls. Differentially expressed genes and weighted gene co-expression network analysis (WGCNA) were combined to identify hub genes. We then conducted Gene Set Enrichment Analysis (GSEA), immune cell infiltration analysis (CIBERSORT), and receiver operating characteristic (ROC) curve analysis to assess the hub gene’s biological function, immune context, and diagnostic performance. Drug-gene interactions were predicted using the DrugBank database. Results: We identified a single key zinc transporter–related hub gene, SLC30A3, which was significantly downregulated in AD and demonstrated potential diagnostic value (AUC 0.70–0.80). Lower SLC30A3 expression was strongly associated with impaired synaptic plasticity (long-term potentiation, long-term depression, calcium signaling pathway, and axon guidance), mitochondrial dysfunction (the citrate cycle and oxidative phosphorylation), and pathways common to major neurodegenerative diseases (Parkinson’s disease, AD, Huntington’s disease, and amyotrophic lateral sclerosis). Furthermore, SLC30A3 expression correlated with specific immune infiltrates, particularly the microglia-related chemokine CX3CL1. Zinc chloride and zinc sulfate were identified as potential pharmacological modulators. Conclusions: Our study systematically identifies SLC30A3 as a novel biomarker in AD, linking zinc dyshomeostasis to synaptic failure, metabolic impairment, and neuroimmune dysregulation. These findings offer a new basis for developing targeted diagnostic and therapeutic strategies for AD. Full article

By accelerating the migration of sulfate ions in potassium magnesium phosphate cement (PMPC) paste through an electric field, its sulfate resistance can be quickly evaluated, thereby making up for the defect of long test cycles in existing evaluation methods. Through sulfate concentration analysis, strength tests, microanalysis and theoretical analysis, this paper investigated the SO₄²⁻ migration behavior of PMPC specimens subjected to electro-pulse-accelerated corrosion. The conclusions are as follows: the distribution of SO₄²⁻ concentration c (x, t) in PMPC specimens followed a polynomial pattern with corrosion period t. The surface SO₄²⁻ concentration c (0, t), measured SO₄²⁻ migration depth h₀, and c (x, t) of specimens increased with the t. After 56 days, the c (0, 56 days) and h₀ of the PN containing nickel slag powder and the PS containing silica fume were lower than that of the reference P0. Their calculated SO₄²⁻ migration depth h₀₀ and SO₄²⁻ migration coefficient D were smaller than that of P0. The h₀₀ and D could be estimated based on t due to a logarithmic relationship between t and h₀₀, D. The strength of specimens at the pulse cathode end gradually improved with t. The 56-day strength for P0, PN, and PS specimens increased by 7.14%, 7.94%, and 8.42%, respectively. The research findings provided a theoretical foundation for the application and quality evaluation of PMPC-based material. Full article

In this research, we examined the potential sensor characteristics of branched polyethyleneimine (BPEI)-derived carbon dots (CDs) synthesized using BPEI as a nitrogen source and citric acid (CA) as a carbon source, specifically for the recognition of various metal ions. Among the BPEI CDs produced with different amounts of BPEI to CA BPEI:CA ratios of 0.5:1, 1:1, and 2:1 w/w, named as BPEI^0.5 CD, BPEI¹ CD, and BPEI² CD, respectively. The BPEI^0.5 CD, which contains the least BPEI, exhibited the highest fluorescence intensity: 50,300 a.u. in a 0.6 mg/mL solution were recorded as λ_em: 420 nm at λ_ex: 360 nm and 600 V PMT voltage with 5 nm of slit width for both excitation and emission. We investigated the fluorescence variations in BPEI CD-based CDs in 2 mL solutions containing Cd²⁺, Co²⁺, Cu²⁺, Ni²⁺, and Pb²⁺ metal ions at various concentrations. Amongst these metal ions, the most pronounced sensitivity was noted for Cu²⁺ ions with a limit of detection (LOD) value of 0.39 ppm. For BPEI CDs created with BPEI:CA ratios of 0.5:1, 1:1, and 2:1 w/w, the sensitivity to Cu²⁺ ions increased with a higher BPEI ratio, with a LOD value of 0.30 ppm recorded for BPEI² CDs. Moreover, Cu²⁺ ion solutions were prepared from various salts, including chloride, acetate, nitrate, and sulfate; aside from some fluorescence variation observed for BPEI^0.5 CDs, no significant difference in BPEI CD fluorescence change was observed with the use of the various salt solutions of Cu²⁺ ion. In quenching experiments conducted on mixtures of Cd²⁺, Co²⁺, Cu²⁺, Ni²⁺, and Pb²⁺ metal ions with Cu²⁺, it was noted that BPEI CDs displayed selectivity for Cu²⁺ ions. Furthermore, the structures of BPEI CDs have been effectively utilized in real water samples, such as tap water and seawater, demonstrating a quenching capability of over 65% in the presence of 50 ppm Cu²⁺ ions. Full article

Perlecan, a major heparan sulfate proteoglycan in the vascular basement membrane, plays an essential role in maintaining endothelial barrier integrity, regulating fibroblast growth factor-2 signaling, and exerting anticoagulant activity. Although alterations in perlecan expression are implicated in the initiation and progression of atherosclerosis, the upstream regulatory mechanisms remain unclear. In this study, we investigated the effects of extracellular ATP on perlecan expression in vascular endothelial cells. ATP, but not ADP or adenosine, suppressed perlecan expression at both mRNA and protein levels in a time- and concentration-dependent manner. This suppression was recovered by knockdown of P2Y2 receptor (P2Y2R), but not by P2X4 receptor, P2X7 receptor, or P2Y1 receptor knockdown, indicating the selective involvement of P2Y2R. Mechanistically, ATP reduced Akt phosphorylation mediated by P2Y2R, and inhibition of Akt by inhibitors decreased perlecan expression, whereas inhibitors of phosphoinositide 3-kinase, mammalian target of rapamycin complex 1, extracellular signal-regulated kinase, p38 mitogen-activated protein kinase, c-Jun N-terminal kinases did not exhibit this recovery effect. These results suggest that ATP downregulates perlecan synthesis via the P2Y2R-mediated inhibition of Akt signaling. Given that ATP is markedly elevated under pathological conditions, such as inflammation and platelet activation, suppression of perlecan synthesis is an important mechanism by which ATP promotes vascular disease progression. Full article

This study aims to resolve the “secondary activation” challenge when erecting structures over goaf zones by employing a novel grouting and filling material. It delves into the performance degradation of the innovative ECS soil grouting filling material (ESGF material) within the goaf’s ionic erosion context. Erosion tests were performed on ESGF material specimens with varying mix designs to mimic the sulfate and chloride erosion scenarios commonly encountered in practical engineering. The macro-mechanical properties and microstructural changes of ESGF materials under ionic erosion environment were systematically investigated by various testing methods, such as unconfined compressive strength (UCS), SEM, XRD, TG, FTIR, and Raman. The findings indicate that both sulfate and chloride erosion lead to a reduction in the strength of the ESGF material. As erosion progresses, the specimens experience a mass increase followed by a decrease, with their strength exhibiting a consistent downward trend. In sulfate erosion conditions, the buildup of expansion product like ettringite (AFt) and thaumasite (TSA) inflicts substantial internal structural damage. Conversely, Friedel’s salt, the primary product of chloride erosion, exhibits relatively weaker expansiveness, and chloride concentration exerts a less pronounced effect on material degradation. Moreover, the cementitious material content and the proportion of quick-setting component play a significant role in determining the ESGF material’s resistance to erosion. By adjusting the quick-setting components ratio in response to changes in the water content of soft soil, the anti-ion erosion performance of solidified soil can be effectively enhanced. Notably, curing with a 5% sulfate maintenance could significantly improve the erosion resistance of ESGF material. This suggests that ESGF materials can be used without concern for curing issues in high-salinity environments during grouting. The research addresses the root cause of goaf subsidence while facilitating the recycling of solid waste, offering an environmentally friendly solution. Full article