PMID- 19321374 OWN - NLM STAT- MEDLINE DCOM- 20091020 LR - 20090529 IS - 1873-2828 (Electronic) IS - 1350-4177 (Linking) VI - 16 IP - 6 DP - 2009 Aug TI - Physical insights into the sonochemical degradation of recalcitrant organic pollutants with cavitation bubble dynamics. PG - 769-81 LID - 10.1016/j.ultsonch.2009.02.009 [doi] AB - This paper tries to discern the mechanistic features of sonochemical degradation of recalcitrant organic pollutants using five model compounds, viz. phenol (Ph), chlorobenzene (CB), nitrobenzene (NB), p-nitrophenol (PNP) and 2,4-dichlorophenol (2,4-DCP). The sonochemical degradation of the pollutant can occur in three distinct pathways: hydroxylation by ()OH radicals produced from cavitation bubbles (either in the bubble-bulk interfacial region or in the bulk liquid medium), thermal decomposition in cavitation bubble and thermal decomposition at the bubble-liquid interfacial region. With the methodology of coupling experiments under different conditions (which alter the nature of the cavitation phenomena in the bulk liquid medium) with the simulations of radial motion of cavitation bubbles, we have tried to discern the relative contribution of each of the above pathway to overall degradation of the pollutant. Moreover, we have also tried to correlate the predominant degradation mechanism to the physico-chemical properties of the pollutant. The contribution of secondary factors such as probability of radical-pollutant interaction and extent of radical scavenging (or conservation) in the medium has also been identified. Simultaneous analysis of the trends in degradation with different experimental techniques and simulation results reveals interesting mechanistic features of sonochemical degradation of the model pollutants. The physical properties that determine the predominant degradation pathway are vapor pressure, solubility and hydrophobicity. Degradation of Ph occurs mainly by hydroxylation in bulk medium; degradation of CB occurs via thermal decomposition inside the bubble, degradation of PNP occurs via pyrolytic decomposition at bubble interface, while hydroxylation at bubble interface contributes to degradation of NB and 2,4-DCP. FAU - Sivasankar, Thirugnanasambandam AU - Sivasankar T AD - Department of Chemical Engineering, Indian Institute of Technology Guwahati, Guwahati 781 039, Assam, India. FAU - Moholkar, Vijayanand S AU - Moholkar VS LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20090227 PL - Netherlands TA - Ultrason Sonochem JT - Ultrasonics sonochemistry JID - 9433356 RN - 0 (Free Radicals) RN - 0 (Organic Chemicals) RN - 0 (Water Pollutants, Chemical) SB - IM MH - Free Radicals/chemistry MH - Organic Chemicals/*chemistry MH - *Ultrasonics MH - Waste Management/*instrumentation MH - Water Pollutants, Chemical/*chemistry EDAT- 2009/03/27 09:00 MHDA- 2009/10/21 06:00 CRDT- 2009/03/27 09:00 PHST- 2008/12/19 00:00 [received] PHST- 2009/02/06 00:00 [revised] PHST- 2009/02/16 00:00 [accepted] PHST- 2009/03/27 09:00 [entrez] PHST- 2009/03/27 09:00 [pubmed] PHST- 2009/10/21 06:00 [medline] AID - S1350-4177(09)00028-5 [pii] AID - 10.1016/j.ultsonch.2009.02.009 [doi] PST - ppublish SO - Ultrason Sonochem. 2009 Aug;16(6):769-81. doi: 10.1016/j.ultsonch.2009.02.009. Epub 2009 Feb 27.