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All channels and two external surface locations were sampled to evaluate the residual organic and microbial load.
For each experiment, duplicate or triplicate microcosms (160-mL) were prepared in the same way as the viable 2-CP– and 3-CB amended mesocosms and periodically sampled to evaluate the reproducibility of the nucleic acid and chemical data obtained with the mesocosms (Becker 1998).
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Regarding the capacity upper bounds in Sections 3.1 3.2 as benchmarks for the performance assessment, we now analyze the capacity achieved by sampling to evaluate the capacity performance loss due to specific post-processing at the receiver.
However, further evaluation is needed in a larger sample to evaluate the possible effect modification, because the RRs seemed to be more pronounced in low social strata.
Crystalline silicon was used as the standard sample to evaluate the hydrogen concentration.
n-Hexane cracking reaction was carried out over the samples to evaluate the catalytic properties.
The method was applied to field samples to evaluate the residual characteristics of thiacloprid and spirotetramat.
Gel chromatography was performed on selected SF samples to evaluate the sizes of SF PG molecules.
The CD rates of the field-exposed samples were compared to unexposed samples to evaluate the interface degradation.
Few studies have compared with a control sample to evaluate the exact mechanism of the appliance [[10]-[16] [[10]-[16]
Mixtures of DMMP, TEP, and methyl salicylate (representing CWAs) were used as samples to evaluate the efficiency of the column.
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