|
|
|
|
LEADER |
01000naa a22002652 4500 |
001 |
NLM217996450 |
003 |
DE-627 |
005 |
20231224035346.0 |
007 |
cr uuu---uuuuu |
008 |
231224s2012 xx |||||o 00| ||eng c |
024 |
7 |
|
|a 10.1021/la300929g
|2 doi
|
028 |
5 |
2 |
|a pubmed24n0726.xml
|
035 |
|
|
|a (DE-627)NLM217996450
|
035 |
|
|
|a (NLM)22616806
|
040 |
|
|
|a DE-627
|b ger
|c DE-627
|e rakwb
|
041 |
|
|
|a eng
|
100 |
1 |
|
|a He, Di
|e verfasserin
|4 aut
|
245 |
1 |
0 |
|a H2O2-mediated oxidation of zero-valent silver and resultant interactions among silver nanoparticles, silver ions, and reactive oxygen species
|
264 |
|
1 |
|c 2012
|
336 |
|
|
|a Text
|b txt
|2 rdacontent
|
337 |
|
|
|a ƒaComputermedien
|b c
|2 rdamedia
|
338 |
|
|
|a ƒa Online-Ressource
|b cr
|2 rdacarrier
|
500 |
|
|
|a Date Completed 01.11.2012
|
500 |
|
|
|a Date Revised 21.11.2013
|
500 |
|
|
|a published: Print-Electronic
|
500 |
|
|
|a Citation Status MEDLINE
|
520 |
|
|
|a The H(2)O(2)-mediated oxidation of silver nanoparticles (AgNPs) over a range of pH (3.0-14.0) is investigated here, and an electron charging-discharging model capable of describing the experimental results obtained is developed. AgNPs initially react with H(2)O(2) to form Ag(+) and superoxide, with these products subsequently reacting to reform AgNPs (in-situ-formed AgNPs) via an electron charging-discharging mechanism. Our experimental results show that the AgNP reactivity toward H(2)O(2) varies significantly with pH, with the variation at high pH (>10) due particularly to the differences in the reactivity of H(2)O(2) and its conjugate base HO(2)(-) with AgNPs whereas at lower pH (3-10) the pH dependence of H(2)O(2) decay is accounted for, at least in part, by the pH dependence of the rate of superoxide disproportionation. Our results further demonstrate that the in-situ-formed AgNPs resulting from the superoxide-mediated reduction of Ag(+) have a different size and reactivity compared to those of the citrate-stabilized particles initially present. The turnover frequency for AgNPs varies significantly with pH and is as high as 1776.0 min(-1) at pH 11.0, reducing to 144.2 min(-1) at pH 10.0 and 3.2 min(-1) at pH 3.0
|
650 |
|
4 |
|a Journal Article
|
650 |
|
4 |
|a Research Support, Non-U.S. Gov't
|
650 |
|
7 |
|a Cations, Monovalent
|2 NLM
|
650 |
|
7 |
|a Citrates
|2 NLM
|
650 |
|
7 |
|a Reactive Oxygen Species
|2 NLM
|
650 |
|
7 |
|a trisodium citrate
|2 NLM
|
650 |
|
7 |
|a Silver
|2 NLM
|
650 |
|
7 |
|a 3M4G523W1G
|2 NLM
|
650 |
|
7 |
|a Hydrogen Peroxide
|2 NLM
|
650 |
|
7 |
|a BBX060AN9V
|2 NLM
|
650 |
|
7 |
|a Superoxide Dismutase
|2 NLM
|
650 |
|
7 |
|a EC 1.15.1.1
|2 NLM
|
700 |
1 |
|
|a Garg, Shikha
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Waite, T David
|e verfasserin
|4 aut
|
773 |
0 |
8 |
|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1992
|g 28(2012), 27 vom: 10. Juli, Seite 10266-75
|w (DE-627)NLM098181009
|x 1520-5827
|7 nnns
|
773 |
1 |
8 |
|g volume:28
|g year:2012
|g number:27
|g day:10
|g month:07
|g pages:10266-75
|
856 |
4 |
0 |
|u http://dx.doi.org/10.1021/la300929g
|3 Volltext
|
912 |
|
|
|a GBV_USEFLAG_A
|
912 |
|
|
|a SYSFLAG_A
|
912 |
|
|
|a GBV_NLM
|
912 |
|
|
|a GBV_ILN_22
|
912 |
|
|
|a GBV_ILN_350
|
912 |
|
|
|a GBV_ILN_721
|
951 |
|
|
|a AR
|
952 |
|
|
|d 28
|j 2012
|e 27
|b 10
|c 07
|h 10266-75
|