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ABSTRACT In this study, we investigate the PFOA removal capabilities ofRhodopseudomonas palustris(R. palustris), a fluoroacetate dehalogenase containing microbe as a potential candidate for achieving bioremediation. In the 50-day PFOA uptake experiment, R. palustris removed 44 ± 6.34 % PFOA after 20 days of incubation, which was then reduced to a final removal of 6.23 ± 12.75 %. Results indicate PFOA was temporarily incorporated into the cell membrane before being released partially into the media after cell lysis. This incorporation might be attributed to the combined effect of hydrophobic interaction between PFOA and the cell membrane and the reduced electrostatic repulsion from the high ion presence in the growth medium. The growth ofR. palustrisduring the PFOA uptake experiment was 9-fold slower than their growth without PFOA. This study also completely defines the toxicity range of PFOA forR. palustristhrough a toxicity assay. Increasing PFOA concentration reduced the microbe growth, with complete inhibition around 200 ppm. For various concentrations of PFOA, R. palustris exhibits interesting diauxic growth behavior. An accelerated growth phase was followed by a temporary death phase in the first 24 hours in the presence of 12.5-100 ppm PFOA, implying a unique adaptation mechanism to PFOA. 

Abstract We report the exfoliation process optimization, physicochemical characterizations, and comparative aggregation behavior of the inorganic 2D nanomaterial hexagonal Boron Nitride (h-BN) produced from two repetitive sonication-centrifugation processes with varying centrifugation speeds and recycle frequency: Continuous and Segmented protocols. Enhancing exfoliation efficiency and understanding aqueous stability are essential for sustainable design and environmental applications. Results showed that the Segmented protocol outperformed the Continuous protocol by having a six-fold increase in the exfoliated h-BN nanosheet yield by reusing the unexfoliated bulk h-BN and decreasing centrifugation speeds. Centrifugation speeds of 1880 and 950 rpm produced nanosheets of similar sizes due to the slight difference in the centrifugal force generated in both protocols. Moreover, nanosheets from both protocols had enhanced polarity due to the higher amounts of −OH bonds attached to the exposed edges of the nanosheets. However, the hydroxylation percentage of the nanosheets decreased with centrifugation speed. Both protocols produced h-BN nanosheets that were stable in DI water dispersion. The comparatively lower initial aggregation rate at all centrifugation speeds supported the fact that the Segmented protocol nanosheets were more stable than the Continuous ones. The Segmented protocol h-BN nanosheets showed better overall stability at lower speeds than the other centrifugation speeds. Segmented protocol nanosheets from 3750 rpm had the lowest aggregation rate than the other centrifugation speed. These findings assist in finding the balance between exfoliation protocol, environmental application, and implication of h-BN nanosheets. 

The removal of small molecular weight charged compounds from aqueous solutions using membrane remains a challenge. In this study, polysulfone (PSf)- and sulfonated polyether ether ketone (SPEEK)-based membranes were fabricated via non-solvent induced phase separation process (NIPS) using N-Methyl-2-Pyrrolidone (NMP) as solvent and water as non-solvent. Membranes were characterized structurally and morphologically, followed by toxicity assessment conducted before and after filtration, both with and without annealing at various pH values to evaluate potential leaching of trapped solvent from the membrane pores. Additionally, membrane performance was characterized using binary mixtures of cationic and anionic dyes. The results demonstrated selective filtration behavior, with cationic dyes being preferentially rejected due to size exclusion and electrostatic interactions. Additionally, a key focus of this work was the investigation of solvent leaching, framed within a Safe(r)-by-Design (SbD) approach aimed at enhancing functional performance while minimizing environmental toxicity. Toxicity assessments using a model organism, a nematode Caenorhabditis elegans, revealed that annealing reduced solvent leaching and thus permeate toxicity, particularly at neutral pH values, by facilitating trapped solvent release prior to membrane use. These findings provide insights for the importance of including an SbD approach during membrane casting to fabricate membranes with desirable properties while minimizing toxicity. 

Graphene-based 3D macroscopic aerogels with their hierarchical porous structures and mechanical strength have been widely explored for removing contaminants from water. However, their large-scale manufacturing and application in various water treatment processes are limited by their scalability. In this study, we report a proof-of-concept direct ink writing (DIW) 3D printing technique and subsequent freeze-drying to prepare graphene-biopolymer aerogels for water treatment. To provide appropriate rheology for DIW printability, two bio-inspired polymers, polydopamine (PDA) and bovine serum albumin (BSA), were added to the graphene-based ink. The biopolymers also contributed to the contaminant removal capacity of the resultant graphene-polydopamine-bovine serum albumin (G-PDA-BSA) aerogel. The physicochemical properties of the aerogel were thoroughly characterized from the nano- to macroscale. The 3D printed aerogel exhibited excellent water contaminant removal performance for heavy metals (Cr( vi ), Pb( ii )), organic dyes (cationic methylene blue and anionic Evans blue), and organic solvents ( n -hexane, n -heptane, and toluene) in batch adsorption studies. The electrostatic interaction dominated the removal of heavy metals and dyes while the hydrophobic interaction dominated the removal of organic solvents from water. Moreover, the aerogel showed superb regeneration and reuse potential. The aerogel removed 100% organic solvents over 10 cycles of regeneration and reuse; additionally, the removal efficiencies for methylene blue decreased by 2–20% after the third cycle. The fit-for-design 3D printed aerogel was also effectively used as a bottle-cap flow-through filter for dye removal. The potential and vision of the 3D printing approach for graphene-based water treatment presented here can be extended to other functional nanomaterials, can enable shape-specific applications of fit-for-purpose adsorbents/reactors and point-of-use filters, and can materialize the large-scale manufacturing of nano-enabled water treatment devices and technologies.