Kinetics of Biochemical Reactions and Microbial Processes in Natural Waters

Author(s):  
Patrick L. Brezonik
2011 ◽  
Vol 45 (8) ◽  
pp. 2517-2526 ◽  
Author(s):  
Pamela Chelme-Ayala ◽  
Mohamed Gamal El-Din ◽  
Daniel W. Smith ◽  
Craig D. Adams

2008 ◽  
Vol 72 (5) ◽  
pp. 1335-1349 ◽  
Author(s):  
Manabu Fujii ◽  
Andrew L. Rose ◽  
T. David Waite ◽  
Tatsuo Omura

1995 ◽  
Vol 29 (1) ◽  
pp. 59-68 ◽  
Author(s):  
Hanbin. Xue ◽  
Laura. Sigg ◽  
Franz Guenter. Kari

2021 ◽  
Author(s):  
Lee Moores ◽  
Stacy Jones ◽  
Garrett George ◽  
David Henderson ◽  
Timothy Schutt

Herein the matrix effects on the kinetics of aqueous photolysis for the individual munitions constituents of IMX-101: nitroguanidine (NQ), dinitroanisole (DNAN), and nitrotriazolone (NTO) are reported along with the environmentally relevant kinetics and quantum yields. Photolysis potentially represents a major degradation pathway for these munitions in the environment and further understanding the complex matrices effects on photolytic kinetics was needed. Aqueous systems are of particular interest due to the high solubility of NQ (3,800 ppm) and NTO (16,642 ppm) compared to the traditional munitions trinitrotoluene (TNT, 100.5 ppm) and 1,3,5-trinitro-1,3,5-triazine (RDX, 59.9 ppm). Environmental half-lives (and quantum yields) were found to be 0.44 days, 0.83 days, and 4.4 days for NQ, DNAN, and NTO, respectively, under natural sunlight. In laboratory experiments using nominally 300 nm bulbs in a merry-go-round style reactor in DI water the relative rate of photolysis for the three munitions constituents followed the same order NQ > DNAN > NTO, where DNAN and NTO reacted 57 and 115 times more slowly, respectively, than NQ. In the various environmentally relevant matrices tested in the laboratory experiments NQ was not significantly affected, DNAN showed a faster degradation with increasing ionic strength, and NTO showed a modest salinity and pH dependence on its rate of photolysis.


2012 ◽  
Vol 560-561 ◽  
pp. 395-400
Author(s):  
Alexander Scheeline ◽  
Woo Hyuck Choi ◽  
Edward T. Chainani ◽  
Khan T. Ngo

Ultrasonically-levitated drops have been widely studied for materials processing and for sample preparation for chemical analysis. We report on the development of such drops for study of kinetics of enzyme-catalyzed reactions and other chemical processes. We review how to simply and reliably levitate drops, discuss why such drops are desirable for studying biochemical reactions, especially those generating or consuming free radicals, and report progress towards routine kinetics measurements in microliter drops.


Water ◽  
2019 ◽  
Vol 11 (5) ◽  
pp. 1001 ◽  
Author(s):  
Joanna Karpinska ◽  
Aneta Sokol ◽  
Jolanta Koldys ◽  
Artur Ratkiewicz

The photochemical behavior of doxazosin (DOX) in simulated environmental conditions using natural waters taken from local rivers as a solvent was studied. The chemical characteristics of applied waters was done and a correlation analysis was used to explain the impact of individual parameters of matrix on the rate of the DOX degradation. It was stated that DOX is a photoliable compound in an aqueous environment. Its degradation is promoted by basic medium, presence of environmentally important ions such as Cl−, NO3−, SO42− and organic matter. The kinetics of DOX reactions with OH− and SO4− radicals were examined individually. The UV/H2O2, classical Fenton and photo-Fenton processes, were applied for the generation of hydroxyl radicals while the UV/VIS:Fe2(SO4)3:Na2SO2 system was employed for production of SO4− radicals. The obtained results pointed that photo-Fenton, as well as UV/VIS:Fe2(SO4)3:Na2SO2, are very reactive in ratio to DOX, leading to its complete degradation in a short time. A quantitative density functional theory (DFT) mechanistic study was carried out in order to explain the molecular mechanism of DOX degradation using the GAUSSIAN 09 program.


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