Photocatalytic and Antimicrobial Properties of ZnO and Mg-Doped ZnO Nanoparticles Synthesized Using Lupinus albus Leaf Extract.

Dye effluents discharged from various industries contribute to environmental contamination, making their treatment highly necessary. Infectious diseases also pose a threat to public health worldwide. Nanomaterials have promising features and are potential candidates for overcoming the problems of drug resistance in microbes and environmental pollution. Therefore, this study aimed to synthesize zinc oxide (ZnO) and magnesium-doped zinc oxide (Mg-doped ZnO) nanoparticles (NPs) using the plant extract of Lupinus albus for applications in photocatalysis and antimicrobial activity. A sample of Lupinus albus leaves was collected from Motta, in the eastern Gojjam zone of Ethiopia. The leaves were air-dried and then ground into a powder. The powdered plant material was extracted using distilled water. The ZnO and Mg-doped ZnO NPs were synthesized using 0.1 M Zn(NO3)2·6H2O, 7.5% 0.1 M Mg(NO3)2.6H2O, and 10 mL of the leaf extract. The nanoparticles (NPs) were characterized using UV-vis, FT-IR, XRD, and SEM. The average crystallite sizes of ZnO and Mg-doped ZnO NPs were determined using the Debye-Scherrer formula and were found to be 28.1 and 34.4 nm, respectively. The antimicrobial activity of the synthesized NPs was evaluated against four bacterial strains (Escherichia coli, Bacillus cereus, Salmonella typhi, and Staphylococcus aureus) and one fungal strain (Candida albicans) by using the agar disk diffusion method. The Mg-doped ZnO NPs exhibited significant antimicrobial activity, with a maximum zone of inhibition measuring 24 and 22 mm against Escherichia coli and Salmonella typhi, respectively. The photocatalytic activity of ZnO and Mg-doped ZnO NPs was investigated by studying the degradation of methylene blue (MB) dye under sunlight irradiation for 120 min. The results showed that Mg-doped ZnO NPs exhibited higher photocatalytic activity (99.6%) than ZnO NPs (94.1%). In conclusion, the synthesized NPs could serve as viable alternatives for antimicrobial drugs and photocatalysts to mitigate the pollution of the environment caused by organic dyes.

Removal of Cr(VI) from Aqueous Solutions Using Biowastes: Tella Residue and Pea (Pisum sativum) Seed Shell.

The wide use of chromium (Cr) in different industries led to the release of a considerable amount of Cr(VI) into water bodies. Exposure to Cr(VI) can cause diseases in humans and animals. Therefore, low-cost technology for Cr(VI) removal is required. In this study, the biowastes, "Tella" residue (TR) and Pea (Pisum sativum) seed shell (PSS), were evaluated for their Cr(VI) removal efficiency from aqueous solutions. The physicochemical properties of adsorbents were studied, and the adsorbents were further characterized using FTIR and XRD. Batch adsorption experiments have shown that the Cr(VI) uptake was pH-dependent and found to be effective in a wide range of pH values (pH 1 to 10) for PSS. The kinetics of Cr(VI) removal by the adsorbents was well expressed by the pseudo-second-order model. The experimental equilibrium adsorption data fitted well with Freundlich isotherm indicating multilayers adsorption. The estimated Cr(VI) adsorption capacities of TR and PSS were 15.6 mg/g and 8.5 mg/g, respectively. On top of this, the possibility of reusing adsorbents indicates the potential applicability of TR and PSS for the treatment of Cr(VI) contaminated water. Further study on the evaluation of the efficiency of the adsorbents using real chromium-contaminated wastewater is recommended.

Hepatoprotective Effect of Corm of Ensete ventricosum (Welw.) Cheesman Extract against Isoniazid and Rifampicin Induced Hepatotoxicity in Swiss Albino Mice.

Drug-induced liver injury (DILI) is one of the cumbersome health-related problems which render approximately 50% of liver failure and patients to receiving liver transplantation every year. Antituberculosis drugs such as isoniazid and rifampicin are potentially rendering hepatotoxicity. Ensete ventricosum (Welw.) Cheesman is an herbaceous perennial plant that contributes to the indigenous ethnomedicinal values for the society. This study aimed to investigate the hepatoprotective effect of corm of Ensete ventricosum (Welw.) Cheesman extracts against isoniazid and rifampicin induced hepatotoxicity in Swiss albino mice. The study was conducted on 30 Swiss albino mice randomly allocated into five groups. Group I, group II, group III, group IV, and group V were the groups in which mice were given distilled water, only isoniazid and rifampicin, isoniazid and rifampicin along with 200 mg/kg corm of Ensete ventricosum (Welw.) Cheesman extract, isoniazid and rifampicin along with 400 mg/kg corm of Ensete ventricosum (Welw.) Cheesman extract, and isoniazid and rifampicin along with silymarin per oral per day, respectively. On the 30th day of the experiment, mice were sacrificed after anesthetized, and blood was drawn for the liver function test, and the liver was also taken from each experimental mouse for histopathological evaluation. Data were entered into EpiData version 3.1 subsequently exported to SPSS version 25 for analysis by using one-way ANOVA. Plasma alanine aminotransferase (ALT) levels, aspartate aminotransferase (AST), alkaline phosphatase (ALP), and total bilirubin (TBIL) of group II mice were significantly (p < 0.05) elevated as compared to group I. The group of mice treated with a corm of Ensete ventricosum (Welw.) Cheesman at a dose of 400 mg/kg (group IV) and silymarin100 mg/kg (group V) showed a significant (p < 0.05) decrease in ALT, AST, ALP, and TBIL as compared to the group II. The liver section of group II showed a change in liver architecture; however, these deformities were not noticed in group IV mice. The result showed corm of Ensete ventricosum (Welw.) Cheesman extract has a very promising hepatoprotective potential against isoniazid and rifampicin induced liver injury.

Spectroscopic Determination of Fluoride Using Eriochrome Black T (EBT) as a Spectrophotometric Reagent from Groundwater.

Fluoride health problem is a great concern worldwide, most often as a result of groundwater intake. Thus, determination of fluoride is vital to take appropriate measures upon fluoride contamination of water. Potentiometric method of analysis is reliable for the determination of fluoride in various samples. In addition, spectroscopic methods are found important to quantify fluoride levels from water; however, several factors hinder its easier determination. Among the bottlenecks, the use of toxic chemicals and tedious steps in preparing chemicals (e.g., SPADNS method) are to mention a few. In this study, a spectrophotometric method was developed for the determination of fluoride from groundwater using Eriochrome Black T (EBT) as a spectroscopic reagent. Experimental parameters that influence the determination of fluoride including ligand type, kinetics, pH, and ligand-to-metal ratio were assayed. Evaluation of fluoride levels showed that Beer-Lambert's law is obeyed in the range of 0.3-5.0 mg/L at 544 nm. The calibration curve, resulting in good linearity (R 2 = 0.9997), was considered during quantitative analysis of the samples and in the spiking analysis. The limits of detection (LOD) and quantification (LOQ) of the method were found to be 0.19 and 0.64 mg/L, respectively. The precision studied in terms of intraday and interday at three concentration levels showed less than 5.4% RSD. Applicability of the method was investigated by analyzing groundwater samples spiked with fluoride standards, and satisfactory recoveries in the range of 98.18-111.4 were demonstrated. The developed spectrophotometric method has been successfully applied for fluoride determinations in groundwater samples. Thus, it could be used as an attractive alternative for the determination of fluoride from groundwater.

Use of (modified) natural adsorbents for arsenic remediation: A review.

Arsenic (As) is a ubiquitous element found in the atmosphere, soils and rocks, natural waters and organisms. It is one of the most toxic elements and has been classified as a human carcinogen (group I). Arsenic contamination in the groundwater has been observed in >70 countries, like Bangladesh, India, West Bengal, Myanmar, Pakistan, Vietnam, Nepal, Cambodia, United States and China. About 200 million people are being exposed to excessive As through consumption of contaminated drinking water. Therefore, developing affordable and efficient techniques to remove As from drinking water is critical to protect human health. The currently available technologies include coagulation-flocculation, adsorption, ion exchange, electrochemical conversion and membrane technologies. However, most of the aforementioned treatment techniques require high initial and maintenance costs, and skilled manpower on top of that. Nowadays, adsorption has been accepted as a suitable removal technology, particularly for developing regions, because of its simple operation, potential for regeneration, and little toxic sludge generation. Processes based on the use of natural, locally available adsorbents are considered to be more accessible for developing countries, have a lower investment cost and a lower environmental impact (CO2 emission). To increase their performance, these materials may be chemically modified. Hence, this review paper presents progress of adsorption technologies for remediation of As contaminated water using chemically modified natural materials.

Removal of Arsenic (V) from Aqueous Solutions Using Chitosan-Red Scoria and Chitosan-Pumice Blends.

In different regions across the globe, elevated arsenic contents in the groundwater constitute a major health problem. In this work, a biopolymer chitosan has been blended with volcanic rocks (red scoria and pumice) for arsenic (V) removal. The effect of three blending ratios of chitosan and volcanic rocks (1:2, 1:5 and 1:10) on arsenic removal has been studied. The optimal blending ratio was 1:5 (chitosan: volcanic rocks) with maximum adsorption capacity of 0.72 mg/g and 0.71 mg/g for chitosan: red scoria (Ch-Rs) and chitosan: pumice (Ch-Pu), respectively. The experimental adsorption data fitted well a Langmuir isotherm (R² > 0.99) and followed pseudo-second-order kinetics. The high stability of the materials and their high arsenic (V) removal efficiency (~93%) in a wide pH range (4 to 10) are useful for real field applications. Moreover, the blends could be regenerated using 0.05 M NaOH and used for several cycles without losing their original arsenic removal efficiency. The results of the study demonstrate that chitosan-volcanic rock blends should be further explored as a potential sustainable solution for removal of arsenic (V) from water.

Adsorption of As(III) versus As(V) from aqueous solutions by cerium-loaded volcanic rocks.

Contamination of drinking water with arsenic causes severe health problems in various world regions. Arsenic exists predominantly as As(III) and As(V) depending on the prevailing redox conditions of the environment. Most of the techniques developed for treating As(V) are not very effective for As(III), which is more toxic and mobile than As(V). In this study, novel cerium-loaded pumice (Ce-Pu) and red scoria (Ce-Rs) adsorbents were developed to remove both As(III) and As(V) ions from water. The Ce-Pu and Ce-Rs adsorbents were characterized using ICP-OES, EDX, and SEM. The experimental equilibrium sorption data fitted well Freundlich and Dubinin-Radushkevich (D-R) isotherms. The adsorption was very fast and reached an equilibrium within 2 h. Both Ce-Rs and Ce-Pu showed high As(III) and As(V) removal efficiency in a wide pH range between 3 and 9, which is an important asset for practical applications. The Ce-Pu and Ce-Rs adsorbents can be recycled and used up to three adsorption cycles without significant loss of their original efficiency. Accordingly, Ce-Pu and Ce-Rs seem to be suitable for removal of arsenic from aqueous systems.