PMID- 26461459 OWN - NLM STAT- MEDLINE DCOM- 20160621 LR - 20181202 IS - 1520-5851 (Electronic) IS - 0013-936X (Linking) VI - 49 IP - 22 DP - 2015 Nov 17 TI - Heteroaggregation of Cerium Oxide Nanoparticles and Nanoparticles of Pyrolyzed Biomass. PG - 13294-303 LID - 10.1021/acs.est.5b03541 [doi] AB - Heteroaggregation with indigenous particles is critical to the environmental mobility of engineered nanomaterials (ENM). We studied heteroaggregation of ceria nanoparticles (n-CeO2), as a model for metal oxide ENM, with nanoparticles of pyrogenic carbonaceous material (n-PCM) derived from pecan shell biochar, a model for natural chars and human-made chars used in soil remediation and agriculture. The TEM and STEM images of n-PCM identify both hard and soft particles, both C-rich and C,O,Ca-containing particles (with CaCO3 crystals), both amorphous and "onion-skin" C-rich particles, and traces of nanotubes. Heteroaggregation was evaluated at constant n-CeO2, variable n-PCM concentration by monitoring hydrodynamic diameter by dynamic light scattering and zeta-potential under conditions where n-PCM is "invisible". At pH 5.3, where n-CeO2 and n-PCM are positively and negatively charged, respectively, and each stable to homoaggregation, heteroaggregation is favorable and occurs by a charge neutralization-charge reversal mechanism (CNCR): in this mechanism, primary heteroaggregates that form in the initial stage are stable at low or high n-PCM concentration due to electrostatic repulsion, but unstable at intermediate n-PCM concentration, leading to secondary heteroaggregation. The greatest instability coincides with full charge neutralization. At pH 7.1, where n-CeO2 is neutral and unstable alone, and n-PCM is negative and stable alone, heteroaggregation occurs by a charge-accumulation, core-shell stabilization (CACS) mechanism: n-PCM binds to and forms a negatively charged shell on the neutral surface of the nascent n-CeO2 core, stabilizing the core-shell heteraggregate at a size that decreases with n-PCM concentration. The CNCR and CACS mechanisms give fundamental insight into heteroaggregation between oppositely charged, and between neutral and charged nanoparticles. FAU - Yi, Peng AU - Yi P AD - Department of Environmental Sciences, The Connecticut Agricultural Experiment Station , New Haven, Connecticut 06511, United States. AD - Department of Civil, Environmental and Geomatics Engineering, Florida Atlantic University , Boca Raton, Florida 33431, United States. FAU - Pignatello, Joseph J AU - Pignatello JJ AD - Department of Environmental Sciences, The Connecticut Agricultural Experiment Station , New Haven, Connecticut 06511, United States. FAU - Uchimiya, Minori AU - Uchimiya M AD - Agricultural Research Service, United States Department of Agriculture , 1100 Robert E. Lee Boulevard, New Orleans, Louisiana 70124, United States. FAU - White, Jason C AU - White JC AD - Department of Analytical Chemistry, The Connecticut Agricultural Experiment Station , New Haven, Connecticut 06511, United States. LA - eng PT - Journal Article PT - Research Support, U.S. Gov't, Non-P.H.S. DEP - 20151027 PL - United States TA - Environ Sci Technol JT - Environmental science & technology JID - 0213155 RN - 0 (biochar) RN - 16291-96-6 (Charcoal) RN - 30K4522N6T (Cerium) RN - 619G5K328Y (ceric oxide) RN - H0G9379FGK (Calcium Carbonate) SB - IM MH - Biomass MH - Calcium Carbonate/chemistry MH - Carya/chemistry MH - Cerium/*chemistry MH - Charcoal/chemistry MH - Hydrogen-Ion Concentration MH - Microscopy, Electron, Transmission MH - Nanoparticles/*chemistry MH - Nanostructures/chemistry MH - Static Electricity EDAT- 2015/10/16 06:00 MHDA- 2016/06/22 06:00 CRDT- 2015/10/14 06:00 PHST- 2015/10/14 06:00 [entrez] PHST- 2015/10/16 06:00 [pubmed] PHST- 2016/06/22 06:00 [medline] AID - 10.1021/acs.est.5b03541 [doi] PST - ppublish SO - Environ Sci Technol. 2015 Nov 17;49(22):13294-303. doi: 10.1021/acs.est.5b03541. Epub 2015 Oct 27.