Mechanistic studies of phytoremediative eradication of brilliant green dye from water by acid-treated Acacia concinna lignocellulosic waste.

A rapidly growing problem for life on earth is contamination of fresh water which is addressed in this article. By taking a glimpse on the causes of contaminations, persistent organic pollutants, especially synthetic dyes got prominent role. Here, out of commonly used techniques, adsorption using plant wastes was chosen for phytofiltration of such dyes. A natural adsorbent from plant source was selected and processed with acid, characterized with FTIR and SEM and then checked the efficacy on cationic dye brilliant green. Phytofiltration of dye was done to check the effectivity of both untreated (OA) and acid treated (OA-AC) form of Acacia concinna biowaste. Results were obtained, evaluated and presented here, giving maximum adsorption capacities (Qm) of AC and OA-AC 95.24 and 909.09 mg.g-1, respectively following Langmuir, pseudo second order kinetics and spontaneous exothermic nature, indicating their suitability to adopt on larger scale wastewater treatment effectively using green technology.

In this work, Acacia concinna both in untreated and acid treated form is used as an efficient adsorbent for the removal of Brilliant green dye from waste water, as not reported earlier, which proves its novelty. The values of adsorption capacities of both the adsorbent types are compared with different natural and synthetic adsorbents reported earlier, this comparison elaborate the efficacy of AC to be used as adsorbent and consider it as one of the efficient adsorbent materials naturally available.

Sorptive removal of diamond green dye by acid treated Punica granatum peels in eco-friendly way.

In this study, acid treated Punica granatum (PG) peels were used for effective removal of Diamond green (DG) dye, commonly found in textile industry waste. Acid treatment enhanced the efficiency of this process along with increasing shelf life and stability of bio-adsorbent by reducing fungal attack risk. Optimized operational parameters for removing DG dye using PG peels powder were: 35-minute contact time, 75 rpm agitation speed, 50°C temperature and pH of 2. Isothermal study results showed that maximum dye removing capacity was 29.08 mg/g. ΔG and ΔH values were -6.384 and -0.05 kJ/mol, respectively indicating that DG dye adsorption on acid treated PG peels is spontaneous and exothermic in nature. It was found that for batch scale adsorptive removal of basic dyes like DG, acid treated Punica granatum peels were effective bio-waste that can be used from our indigenous sources in an effective way.

A novel route for preparation of chemically activated carbon from pistachio wood for highly efficient Pb(II) sorption.

Pistachio wood-derived activated carbon prepared by a two-stage process (PWAC-2), conducting two consecutive chemical activation processes with NH4NO3 and NaOH, respectively. The results showed that explosive characteristic of NH4NO3 can primarily be employed to produce a char, with a large surface area and a highly-ordered pore structure, which can be subjected to a second activation process with NaOH to prepare a more suitable activated carbon, with a highly porous structure and useful functional groups, for removal of lead ions from aqueous media. An L25 Taguchi experimental design was used by varying impregnation ratio, activation time and temperature in both pre- and post-activation stages, and the results showed that, in both stages, a small activating agent/precursor and a proportional low activation time suffice for preparation of an advantageous activated carbon for Pb(II) adsorption. A comprehensive study was performed on the equilibrium, kinetic and thermodynamic aspects of Pb(II) adsorption by the new activated carbon. The results exhibited that, having had a high lead adsorption capacity (190.2 mg g-1), a high adsorption rapidness, and thermodynamic favorability, PWAC-2 is a beneficial alternative for utilization in full-scale plants of lead removal from waters and wastewaters.

Combined molecular dynamics simulations and experimental studies of the removal of cationic dyes on the eco-friendly adsorbent of activated carbon decorated montmorillonite Mt@AC.

In recent years, the combination of experimental and theoretical study to explain adsorbate/adsorbent interactions has attracted the attention of researchers. In this context, this work aims to study the adsorption of two cationic dyes, namely methylene blue (MB) and crystal violet (CV), on a green adsorbent Montmorillonite@activated carbon (Mt@AC) composite and to explain the adsorption behavior of each dye by the molecular dynamics (MD) simulation method. The eco-friendly nanocomposite Mt@AC is synthesized and characterized by the analysis methods: XRD, FTIR, BET, TGA/DTA, SEM-EDS, EDS-mapping and zeta potential. The experimental results of adsorption equilibrium show that the adsorption of the two dyes is well suited to the Langmuir adsorption model. The maximum adsorption capacity of the two dyes reaches 801.7 mg g-1 for methylene blue and 1110.8 mg g-1 for crystal violet. The experimental kinetics data fit well with a pseudo-first order kinetic model for the two dyes with coefficient of determination R 2 close to unity, non-linear chi-square χ 2 close to zero and lower Root Mean Square Error RMSE (R 2 → 1 and χ 2 → 0, RMSE lower). Molecular dynamic simulations are run to gain insights on the adsorption process. According to the RDF analysis and interaction energy calculations, the obtained results reveal a better affinity of the CV molecule with both the AC sheet and montmorillonite framework as compared with MB. This finding suggests that CV is adsorbed to a larger extent onto the nanocomposite material which is in good agreement with the adsorption isothermal experiment observations.

The dual impact of Jordanian Ephedra alte for inhibiting pepsin and treating microbial infections.

Screening of phytochemical Ephedra alte crude extract by GC-MS and HPLC analysis indicated the presence of alkaloids, tannins, flavonoids, terpenoids, and phenolic acid in the extract. The total phenolic content of E. alte methanol extract was 39.43 mg of Gallic acid eq/g, crude E. alte with 56.74, and 2.42 µg Trolox equivalent antioxidant capacity (TEAC)/g of plant extract according to DPPH and FRAP assay, respectively. The antimicrobial activity of E. alte against Staphylococcus aureus, staphylococcus epidermidis, Escherichia coli, and Klebsiellaoxytoca demonstrated a mean zone diameter of inhibition ranging from 0 to 17 mm. The MIC of the extracts ranged from 0.5 to 1.0 mg/mL. E. alte extract inhibits pepsin enzyme activity with IC50 values of 213.67 µg/ml. This study revealed that E. alte extract has pepsin enzyme inhibitory, antibacterial, antioxidant activities. The current outcomes indicate that E. alte might be employed as a natural agent for managing GERD and infectious diseases.

Kinetic Studies on the Removal of Some Lanthanide Ions from Aqueous Solutions Using Amidoxime-Hydroxamic Acid Polymer.

Lanthanide metal ions make distinctive and essential contributions to recent global proficiency. Extraction and reuse of these ions is of immense significance especially when the supply is restricted. In light of sorption technology, poly(amidoxime-hydroxamic) acid sorbents are synthesized and utilized for the removal of various lanthanide ions (La3+, Nd3+, Sm3+, Gd3+, and Tb3+) from aqueous solutions. The sorption speed of trivalent lanthanides (Ln3+) depending on the contact period is studied by a batch equilibrium method. The results reveal fast rates of metal ion uptake with highest percentage being achieved after 15-30 min. The interaction of poly(amidoxime-hydroxamic) acid sorbent with Ln3+ ions follows the pseudo-second-order kinetic model with a correlation coefficient R2 extremely high and close to unity. Intraparticle diffusion data provide three linear plots indicating that the sorption process is affected by two or more steps, and the intraparticle diffusion rate constants are raised among reduction of ionic radius of the studied lanthanides.