This article examines the influence of three common stabilizing agents (citrate, poly(vinylpyrrolidone) (PVP), and branched poly(ethylenimine) (BPEI)) on the attachment affinity of silver nanoparticles to ceramic water filters. Citrate-stabilized silver nanoparticles were found to have the highest attachment affinity (under conditions in which the surface potential was of opposite sign to the filter). This work demonstrates that the interaction between the electrical double layers plays a critical role in the attachment of nanoparticles to flat surfaces and, in particular, that predictions of double-layer interactions are sensitive to boundary condition assumptions (constant charge vs constant potential). The experimental deposition results can be explained when using different boundary condition assumptions for different stabilizing molecules but not when the same assumption was assumed for all three types of particles. The integration of steric interactions can also explain the experimental deposition results. Particle size was demonstrated to have an effect on the predicted deposition for BPEI-stabilized particles but not for PVP.
Silver nanoparticles are used in a wide variety of consumer products and are therefore rapidly becoming ubiquitous in the natural environment; they can be expected to be found in the natural waters used as drinking water supplies. This research investigated whether such particles could be expected to be removed in conventional water treatment plants such as flocculation and filtration. Both flocculation and granular media filtration experiments with citrate-capped silver nanoparticles were performed at different ionic strengths and in the presence and absence of natural organic matter. The results were generally consistent with theories of particle destabilization that have been developed for larger particles (greater than 1 μm), suggesting that silver nanoparticles are likely to be removed in conventional treatment processes.
In this paper, we performed an experiment with activated carbon manufactured from waste coffee grounds on the compressive strength of normal cement mortars. The activated carbon reinforcement was manufactured from waste coffee grounds, and the collected coffee grounds were then transformed into activated carbon granules through the physical activation process. The activated carbon/cement composites were prepared by mixing cement with activated carbon granules with the weight fractions of 0.5%, 1%, 1.5%, 5%, and 10% cement. The experimental results show that adding activated carbon up to 1.5 wt% increased the early strength of cement mortars. Furthermore, we found that the composites incorporated with a small amount of activated carbon (≤1.5 wt%) had higher compressive strength over the curing period than the normal cement without activated carbon. We believe that these results would potentially have commonalities with morphological symmetry phenomena that occur on the surfaces of activated carbon granules.
The understanding of nano-sized particle separation processes has been limited by difficulties of nanoparticle characterization. In this study, nanoparticle tracking analysis (NTA) was deployed to evaluate the absolute particle size distributions in laboratory scale flocculation and filtration experiments with silver nanoparticles. The results from NTA were consistent with standard theories of particle destabilization and transport. Direct observations of changes in absolute particle size distributions from NTA enhance both qualitative and quantitative understanding of particle separation processes of nano-sized particles.
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