Development of adsorbent from Mentha plant ash and its application in fluoride adsorption from aqueous solution: a mechanism, isotherm, thermodynamic, and kinetics studies.

In the present study, Mentha plant ash was modified by Na and Al for the synthesis of adsorbent and applied for the removal of Fluoride from an aqueous solution. Mixture of acid washed Mentha plant ash (MPA) and NaOH (in the ratio 1:1.3) thermally treated at 600°C in a muffle furnace then treated with aqueous solution of sodium aluminate. The characterization of sodium aluminum modified ash (Na-Al-MA) powder was done such as SEM (Scanning Electron Microscopy), Particle Size Analysis (PSA), Fourier transformed spectroscopy (FTIR), Zeta Potential, XRD (X-ray Diffraction) analysis, and Brunauer-Emmett-Teller (BET) analysis. The removal of fluoride from an aqueous solution carried out with Na-Al-MA by batch adsorption process. The Na-Al-MA was found to be very effective as adsorbent. The maximum removal of fluoride was achieved Ì´ 86% at neutral pH and at room temperature. It was investigated that Langmuir adsorption isotherm and pseudo-second-order kinetic was best fitted for fluoride adsorption. The fluoride adsorption on Na-Al-MA was an exothermic process. A possible mechanism including electrostatic attraction, hydrogen bonding, and metal-fluoride interaction for fluoride adsorption on Na-Al-MA have described in this study. Novelty statement: Utilization of Mentha plant ash for the development of adsorbent and its application in adsorptive removal of fluoride from aqueous solution is the novelty of this work. Adsorbent preparation may be the better way of waste biomass management.

Synergistic action of adsorption and reductive properties of ash derived from distilled Mentha piperita plant waste in removal of Cr(VI) from aqueous solution.

Adsorption behavior of Mentha Plant Ash (MPA) in removal of Cr(VI) from aqueous solution was analyzed as a function of different pH (3.0-8.0), different concentration of Cr(VI) (10-50 mg L-1), contact time (0-90 min) and doses of adsorbent (0.1-0.5 g/100 mL). Adsorption of Cr(VI) onto MPA was found to be dependent on pH condition of the solution and showed maximum removal of Cr(VI) at pH 3.0. The study of adsorption kinetics on Cr(VI) removal by MPA showed that pseudo-second order kinetic model was more suitable to describe the Cr(VI) removal by adsorption onto MPA. Results on Cyclic Voltammetry study of MPA treated with Cr(VI) solution revealed the reduction of Cr(VI) to Cr(III) and Cr(II) by MPA particles through multi-step electron transfer reactions. A combined effect of adsorption and reduction properties of MPA was particularly responsible for removal and transformation of Cr(VI). These attributes of MPA were contributed by many active Cr(VI) binding and electron donating ligands present on the MPA surface as evident from FTIR and XPS analysis of MPA.

Enhanced electrochemical phosphate recovery from livestock wastewater by adjusting pH with plant ash.

In the field of environmental wastewater treatment, it is a very meaningful topic to recover phosphate from swine wastewater in the form of struvite precipitation. The solution pH is one of the important influencing factors in the process of struvite precipitation. In this paper, an attempt was made to recover the phosphate from swine wastewater by adding plant ash. Experimental results have revealed that aeration can be replaced by optimal plant ash adding mode to increase the phosphate recovery efficiency. With the dosages of plant ash and magnesium metal were respectively 11.66 and 3.33 g/L the phosphate recovery efficiency reached 97.69% in 60 min. The efficiency was still above 95% after repeatedly using magnesium pellet for 3 times. The economic evaluation further revealed that the recovery cost of the proposed method was 0.62 $/kg PO4-P.

Highly Efficient Removal of Nitrate and Phosphate to Control Eutrophication by the Dielectrophoresis-Assisted Adsorption Method.

The removal of excessive amounts of nitrate and phosphate from water sources, especially agricultural wastewater, has been of high significance to control eutrophication in aquatic systems. Here, a new method is reported for the removal of nitrate and phosphate simultaneously from wastewater based on the combination of the solution-phased adsorption (ADS) and dielectrophoresis (DEP) techniques. The plant ash was first selected as the adsorbent by screening tests, followed by a systematic investigation of using the adsorbent to remove nitrate and phosphate from wastewater under various experimental conditions, including the testing of adsorbent dosage, pretreatment time, water flow rate, and electrode voltage. The analysis of the adsorbent particles was also performed by scanning electron microscope (SEM) analysis, the energy dispersive X-ray spectroscopy (EDX) test, and the measurement of Zeta potentials. Compared with the ADS method alone, the introduction of DEP into the purification process has greatly increased the removal rate by 66.06% for nitrate and 43.04% for phosphate, respectively. In the meantime, it is observed that the processing time has been greatly reduced by 92% with the assistance of DEP.

On the gelation of Premna microphylla turcz extracts: The effects of supernatant and precipitate of plant ash suspension.

In order to elucidate the gelling mechanism of Premna microphylla turcz (PMT) induced by plant ash (PA), PA was fractionated into supernatant (PA-S) and precipitation (PA-P) and added to the PMT suspension, respectively. The effects of different concentrations (1-9%) and fractions (PA, PA-S, PA-P) of PA suspension on the gel properties were studied. Results showed that the electrical conductivity, content of monovalent cations, pH were higher in PA-S than PA-P. Both the PA-S and PA-P fractions induced the gelation of PMT (except for the low concentration at 1% for PA-S), and the PA-P-PMT gels showed much higher gel strength and hardness than PA-S-PMT gels. With increased concentration, the gel strength increased in PA-P-PMT, but decreased in PA-S-PMT. A hypothesis for the gelation of PMT induced by PA was proposed: the divalent cations in PA bind to carboxyl group in pectin and form gels; when higher content of PA is added, a higher pH leads to extensive dissociation of carboxyl groups thereby increases the electrostatic repulsion between pectin chains, which ultimately weakens the gelling forces. This study can provide theoretical support for further optimization of the traditional processing of PMT gels.

Improvement of Asphalt-Aggregate Adhesion Using Plant Ash Byproduct.

The adhesion bonding between asphalt and aggregate significantly influences field performance and durability of asphalt pavement. Adhesion promoters are typically used to improve asphalt-aggregate bonding and minimize moisture-related pavement damage, such as cracking and raveling. This study evaluated the effectiveness of plant ash byproduct as adhesion promoter to improve asphalt-aggregate adhesion performance. Three commonly used aggregate types (granite, basic rock, and limestone) and two asphalt binder types were used in laboratory testing. A modified stripping test method was developed to evaluate test results with image analysis and measurement of asphalt film thickness. The contact angle test and scanning electron microscopy (SEM) with energy disperse spectroscopy (EDS) were conducted. Test results showed that plant ash lixivium significantly improved asphalt-aggregate adhesion. Among three aggregate types, granite yielded the worst asphalt-aggregate adhesion for both control and treated specimens. The effectiveness of adhesion promotion varied depending on the type of asphalt or aggregate and temperature. The SEM/EDS observations showed that the mesh-like crystalline was formed at the interface between asphalt binder and aggregate in the treated specimen, which was believed to enhance the interfacial bonding and prevent asphalt film peeling off from aggregate.

Retention of barium and europium radionuclides from aqueous solutions on ash-based sorbents by application of radiochemical techniques.

New materials were synthesized for application in sorption of radionuclides from aqueous solutions. The elaboration was performed by conversion of power plant ash using the hydrothermal method under optimum experimental conditions. Sodalite, Na-Y, and analcime were formed from ash precursor during the treatment, exhibiting thermal stability as revealed by the characterization by X-ray diffraction (XRD) and thermogravimetric differential thermal analysis (TG-DTA). The Brunauer-Emmett-Teller (BET) surface area and pore volume were determined and they presented higher values than plant ash. The ability of the new products to retain Ba and Eu radionuclides was studied in aqueous solutions using (133)Ba and (152)Eu as tracers and γ-ray spectroscopy under batch experiments. The experimental data were modeled by the Langmuir and Freundlich equations, whereas sorption kinetics measurements were performed at 293, 308, and 323K and thermodynamic parameters were calculated. The release of the sorbed ions into the environment was also tested by leaching experiments. The results of these tests indicated that the synthesized materials are very efficient in removing the aforementioned metals from aqueous solutions and can be considered as potential low-cost sorbents in nuclear waste management.

Mustard plant ash: a source of micronutrient and an adsorbent for removal of 2,4-dichlorophenoxyacetic acid.

The work highlights the utilization of an agricultural waste mustard plant ash (MPA) as a soil additive and an adsorbent. MPA was characterized by X-ray fluorescence (XRF), energy-dispersive X-ray spectroscopy (EDX), proximate analysis, CHNS analysis, Brunauer-Emmett-Teller (BET) surface area analysis, zeta potential measurements, Fourier transform infrared (FTIR), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). XRF analysis confirmed the presence of CaO (31.35 %), K2O (18.55 %), and P2O5 (6.99 %), all of which act as micronutrients to plants. EDX also confirms high amount of elemental O, Ca, K, and P. The adsorptive ability of MPA was investigated using a commonly used herbicide, 2,4-dichlorophenoxyacetic acid (2,4-D), as a representative chemical. Batch adsorption experiments were conducted to study the effect of different operational parameters such as adsorbent dose, initial 2,4-D concentration, contact time, and temperature on the adsorption process. Data from experiments were fitted to various kinetic and isothermal models. The pseudo-second-order kinetic model was found to show the best fit (R 2 > 0.99), with the highest k 2 value of the order 105. Based on the study results, dosage of MPA/hectare for different crops has been recommended for effective removal of 2,4-D. To our knowledge, this is the first study in which MPA has been characterized in detail and investigated for dual applications (as an adsorbent and as a soil additive).