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To explore the photocatalytic mechanism of the S-doped Sb2O3 nanocrystals, the major oxidative species in the photocatalytic reaction were trapped using p-benzoquinone (BZQ, an O2−· radical scavenger), disodium ethylene diamine tetra acetate (Na2-EDTA, a hole scavenger), and tert-butanol (t-BuOH, a OH· radical scavenger) [39, 45].
Nitrous oxide emissions from soil were trapped using open-bottomed polythene static chambers with a trapping area of 0.03 m2 (18 cm internal diameter, 20 cm height, 1.5 mm wall thickness) described by Holland et al. (1999) and Meyer et al. (2001).
Granulocyte and lymphocytes were trapped using typical power levels of ∼5 mW.
The adults were trapped using mist nets or a net designed for catching birds coming out from the nest cavity.
The naturally-reared fish were trapped using baited minnow traps and sampled during February, April, May and June 2008.
Samples were dissolved in 0.1% TFA and, on the nanoAcquity system, peptides were trapped using a pre-column (Symmetry® C18, 5 µm, 180 µm ×20 mm, Waters) which was then switched in-line to an analytical column (BEH C18,1.7 µm, 75 µm ×250 mm, Waters).
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Although, atoms and particles greater than 100 µm have been reported to be trapped using optical tweezers [94, 95].
Serum pIgA was trapped using mouse Fcα/μR transfectant.
This approach requires that intermediate states be trapped using modified enzymes, inert cofactors, or substrate analogues.
Only lipophilic compounds can be trapped using this method (lipid core nanoparticles).
The hydroxyl radical generated in a standard Fenton reaction was trapped using DMPO according to the method previously described [ 12].
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