7 ± 30.5μA/m

, 376 ± 34.4μW/m

and 5 ± 2.7%, whereas for stage 1 these values were 419 ± 71μA/m

, 52.7 ± 18μW/m

and 0.02%, respectively. A metagenomic analysis – stage 2 – in the anodic chamber, demonstrated that SR was due to

(

),

and

and the electrogenic microorganisms were

,

,

,

, and families

and

.

It was demonstrated that microorganisms prevenient from hydrothermal vent sediments adapted to a microbial fuel cell system are able to generate electricity coupled to 74.3 ± 1.5 and 75.3 ± 9.6% of SR and COD removal respectively, with a mixture of acetate – butyrate.

It was demonstrated that microorganisms prevenient from hydrothermal vent sediments adapted to a microbial fuel cell system are able to generate electricity coupled to 74.3 ± 1.5 and 75.3 ± 9.6% of SR and COD removal respectively, with a mixture of acetate – butyrate.The present work seeks to investigate the kinetics and thermodynamic studies of ethidium bromide (EtBr) and eosin adsorption onto the synthesized Manganese (II) doped Zinc (II) Sulphide nanoparticles. A convenient scheme of co-precipitation was used for the synthesis of Manganese (II) doped Zinc (II) Sulphide nanoparticles. The Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscopy (FESEM) and X-ray diffractogram (XRD) techniques were used for the characterization of synthesized nanoparticles. The adsorption study was undertaken in a systematic manner. Effects of different experimental parameters were studied using batch adsorption method. It was evident from the results that EtBr and eosin removal was inversely proportional to the concentration of initial dye and directly proportional to contact time and adsorbent used. To study the adsorption equilibrium three different isotherm models like Langmuir, Freundlich and Flory-Huggins were used. It was observed that adsorption data synced most successfully with Langmuir isotherm model as compared to Freundlich and Flory-Huggins isotherm model. To fit the investigational statistics, the kinetic models pseudo 1st order, pseudo 2nd order and intra particle diffusion were taken onto consideration. The maximum dye removal of 98.19% and 97.16% for EtBr and eosin, was observed during the synthesis of nanoparticles.This study centers on the controllable synthesis, characterization, and application of a novel magnetic bio-metal-organic framework (Bio-MOF) for the adsorption and subsequent removal of arsenic from aqueous solutions. Zinc ions and carnosine (Car) were exploited to construct the Car-based MOF on the surface of magnetite (Fe3O4 NPs). The Magnetite precoating with Car led to an increase in the yield and the uniform formation of the magnetic MOF. The prepared magnetic Bio-MOF nanoparticles (Fe3O4-Car-MOF NPs) had semi-spherical shape with the size in the range of 35-77 nm, and the crystalline pattern of both magnetite and Car-based MOF. The NPs were employed as an adsorbent for arsenic (As) removal. The adsorption analyses revealed that all studied independent variables including pH, adsorbent dose, and initial arsenic concentration had a significant effect on the arsenic adsorption, and the adsorption data were well matched to the quadratic model. The predicted adsorption values were close to the experimental values confirming the validity of the suggested model. Furthermore, adsorbent dose and pH had a positive effect on arsenic removal, whereas arsenic concentration had a negative effect. The adsorption isotherm and kinetic studies both revealed that As adsorption fitted best to the Freundlich isotherm model. The maximum monolayer adsorption capacity (94.33 mg/g) was achieved at room temperature, pH of 8.5 and adsorbent dose of 0.4 g/L. Finally, the results demonstrated that the adsorbent could be efficiently applied for arsenic removal from aqueous environment.Cerium fluoride (CeF3) nanoparticles (NPs) were synthesized and applied in polysulfone (PS) membrane fabricated by phase inversion method. The produced nanocomposite membranes (PS/CeF3) with different contents of CeF3 NPS (0.25%, 0.5%, 0.75% and 1% w/w) were used to treat pharmaceutical wastewaters. The membranes were characterized by FESEM, EDX, XRD, FTIR, porosity, and water contact angle analyses. Inobrodib Evaluation of the characteristics and performance of the nanocomposite membranes confirmed that utilizing photocatalytic CeF3 NPs in membrane structure could effectively decompose organic contaminants in pharmaceutical wastewaters. It also improves the hydrophilicity and antifouling ability of membrane during filtration especially, in the presence of UV irradiation. The permeate flux of the PS membrane increased from 35.1 to 63.77 l/m2h by embedding 0.75% of CeF3 NPs in membrane structure due to the porosity enhancement from 71.36-78.42% and the decrease in contact angle from 62.9º to 53.73º. Moreover, the flux decline of PS/CeF3-0.75% membrane under UV irradiation was from 63.6 to 46.1 l/m2h that considerably lower than that of the neat PS membrane (from 34.7 to 4.9). On the other hand, the degradation efficiency of PS/CeF3-0.75% membrane was more than 97%, and COD removed was more than 65% while they were 75% and 31%, respectively for the nascent PS membrane. Therefore, applying the appropriate amount of CeF3 NPs in PS membranes not only greatly increased the permeate flux but also significantly enhanced the degradation efficiency and COD removal. This indicates that nanocomposite membranes can be confidently applied for pharmaceutical wastewater treatment UV irradiation.

Ammonium chloride as an explosive salt has proved to be a prominent activation agent for adsorbents and increase the specific surface area and volume of cavities. In this work, the ability of this substance was scrutinized for activation of carbon aerogel to prepare an efficient adsorbent for benzene removal from air streams.

A carbon xerogel was fabricated from Novallac polymer and activated by ammonium chloride.The changes in structure and morphology were considered via Brunauer-Emmett-Teller (BET), scanning electron microscopy (SEM), Fourier transform infrared (FTIR), Barrett-Joyner-Halenda (BJH), and energy dispersive X-ray (EDX) analyses. Also, comprehensive studies were conducted to vouchsafe the properties of the new adsorbent for benzene removal, using a fixed-bed column mode.

The results showed both the successful synthesis and the suitability of the activation process. ACX possessed a higher specific surface area (1008g/m

), compared to the parent carbon xerogel (CX; 543.7g/m

) and organic xerogel (OX; 47g/m

), as well as a higher adsorption capacity.