Abstract Arsenic is a natural compound of metalloid (both metal and non-metal) found in soil and minerals used in semiconductor and alloys. Arsenic exposure is associated with an increased risk of cardiovascular disease (CVD) risk from drinking water or environmental sources. Exploring the emerging biomarkers associated with CVD upon arsenic exposure is crucial. Thus, this review paper aimed to analyze the prediction of emerging CVD biomarkers in population exposed to arsenic and their associated risk factors in humans by a systematic review and meta-analysis. A systematic search was conducted using PubMed, Scopus, and Web of Science to identify eligible studies on arsenic exposure associated with CVDs and their risk factors. Sensitivity, specificity, and predictive value of biomarkers for CVD of arsenic exposed population were assessed by calculating the quality criteria, standard means different (SMD), odds ratio (OR), and 95% confidence intervals (CIs). A meta-analysis was used to derive a combined SMD and OR for the heterogeneity test in between studies. The meta-analysis of nine articles were included. The overall effect sizes revealed significant heterogeneity across studies ( I 2 = 97.57%), with pooled effect size was 3.578 (95% CI 3.032 to 4.123, p < 0.0001) under the random-effects model. These results indicate a robust association between arsenic exposure and adverse cardiovascular outcomes, as confirmed by sensitivity analyses and bias assessments (Systematic review registration: PROSPERO CRD42024616848). To improve the quality of future research, efforts should concentrate on enhancing control for confounders, enrolling diverse participant populations, and implementing and yield more substantial findings concerning the cardiovascular effects of arsenic exposure.
Hybrid systems with immobilized TiO2 within dual-layer hollow fiber membranes are the most promising set-up for photocatalytic applications because they possess advantages in both the degradation and separation processes. The performance of dual-layer hollow fiber membranes may be maximized using a functional material of high performance as the selective layer. This paper reports the influence of polyethyleneglycol (PEG) as a pore forming agent on the structure and performance of dual layer hollow fiber membranes. Titanium dioxide (TiO2) was used as a photocatalyst in the outer layer of dual layer hollow fiber (DLHF) membranes. DLHF membranes were fabricated via a single step co-extrusion technique and characterized in terms of surface roughness, membrane porosity, hydrophilicity, and cross-sectional and surface morphology. Nonylphenol (NP) photocatalytic degradation and filtration were evaluated using a hybrid membrane photoreactor. The experimental results revealed that DL-PEG/TiO2 membrane increases the NP solution flux, while decreasing the incidence of membrane fouling and allowing for a smoother and more hydrophilic membrane surface. The findings show that the addition of PEG in the inner layer of DLHF membranes may enhance flux performance in the photocatalytic process.
The adequacy of uremic toxins removal via hemodialysis treatment is essential for every kidney failure patient. To obtain hemodialysis adequacy, the effects of main polymer were investigated. The hollow fiber membranes were produced by using dry/wet spinning process from dope solution comprising PES as the main polymer, 3% poly(vinyl pyrrolidone) (PVP) in 1-methyl-2-pyrrolidone (NMP) at 40-cm air gap. PES loadings of 14, 16, and 18 wt.% were studied. The membrane morphology was characterized by using a scanning electron microscope (SEM) and the membrane properties were measured by using contact angle measurement (WCA). Membrane performance was evaluated by pure water flux (PWF), retention to bovine serum albumin (BSA), p-cresol and urea removal (URR) by using cross-flow permeation system. SEM analysis showed the asymmetric finger-like structure obtained for each polymer loading. The dense skin layer in the inner surface had thickened, followed by the increasing polymer weight loading. The 14 wt.% PES loading had a better pore size (116 nm) and porosity (74%). The WCA showed that the hollow fiber membranes studied were hydrophilic, and the utilization of 14 wt.% PES loading obtained better PWF (108.58 Lm-2h-1). However, this result had an impact on the impairment of BSA retention. The BSA retention for 14 wt.% PES loadings was 88.23%. The URR and p-cresol removal for 14 wt.% PES loading was higher (80.90% and 36.85% for 4 h, respectively) compared to others. As a conclusion, the percentage weight loading for polymer was a significant influence for morphology, membrane properties, and uremic toxins removal.
In this study, an economic silica based ceramic hollow fiber (HF) microporous membrane was fabricated from guinea cornhusk ash (GCHA). A silica interlayer was coated to form a defect free silica membrane which serves as a support for the formation of thin film composite (TFC) ceramic hollow fiber (HF) membrane for the removal of microplastics (MPs) from aqueous solutions. Polyacrylonitrile (PAN), polyvinyl-chloride (PVC), polyvinylpyrrolidone (PVP) and polymethyl methacrylate (PMMA) are the selected MPs The effects of amine monomer concentration (0.5 wt% and 1 wt%) on the formation of poly (piperazine-amide) layer via interfacial polymerization over the GCHA ceramic support were also investigated. The morphology analysis of TFC GCHA HF membranes revealed the formation of a poly (piperazine-amide) layer with narrow pore arrangement. The pore size of TFC GCHA membrane declined with the formation of poly (piperazine-amide) layer, as evidenced from porosimetry analysis. The increase of amine concentration reduced the porosity and water flux of TFC GCHA HF membranes. During MPs filtration, 1 wt% (piperazine) based TFC GCHA membrane showed a lower transmission percentage of PVP (2.7%) and other suspended MPs also displayed lower transmission. The impact of humic acid and sodium alginate on MPs filtration and seawater pretreatment were also analyzed.
Ceramic hollow fiber membranes (CHFMs) are known for their excellent characteristics including high surface area, compact design, and good chemical, thermal, and mechanical stabilities. Despite these interesting attributes, CHFMs are also prone to certain limitations, such as brittleness and high cost that hinder them from being commercialized. To mitigate this drawback, we have developed a high strength, porous ceramic hollow fiber membrane, derived from mullite–kaolinite powder, for efficient oil–wastewater separation. The superhydrophilic, low-cost mullite-based (CHFM) was successfully fabricated through combined phase inversion and sintering techniques. Prior to the fabrication, the as-received mullite–kaolinite was characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), and Brunauer–Emmett–Teller (BET) analyses. Subsequently, operational parameters such as the effect of mullite content, sintering temperature, and air gap were optimized during the fabrication of mullite ceramic hollow fiber membrane. The resulting membranes were systematically characterized and evaluated in terms of morphology, porosity, mechanical strength, water flux, and oil–water separation. Increasing the mullite content, air gap, and sintering temperature enhanced the formation of microvoid structure. It is interesting to note that the mechanical strength of 86 MPa was obtained for the membrane containing 60 wt % of mullite sintered at 1450 °C and an air gap of 5 cm. The membrane induced a stable permeate water flux and oil rejection of mullite CHFM of 182 L/m2∙h and 97.1%, respectively. As compared to kaolin ceramic counterparts, this porous mullite ceramic hollow fiber membrane can be used in various water treatment applications, including for the separation of oily wastewater due to its mechanical strength and water flux.
This paper presents the work carried out to determine the morphology and mechanical properties of coating deposited layer that formed onto mild steel substrate using a new silicanizing method. The result shows that the coating silicanized layer consisting of FeSi, Fe2SiO4, FeSiO3 and SiO2 phase was successfully formed on the mild steel after subjecting to heat treatment process of 1000 °C for 4 hours. This layer of â��500I¼m thickness and also established that higher temperature and elongated deposition/adhesion time resulted an increase in SiO2 concentration on the substrate (mild steel). ©2006-2016 Asian Research Publishing Network (ARPN).