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From this testing and subsequent testing, ammonia losses from both the absorption and regeneration steps were quantified, and attempts were made to maintain steady state during operations.
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Third, the relative flux of carbon through 15 different metabolic steps was quantified (Figs. 1, 2).
Thus secondly the environmental impacts (water consumption and CO2 emission) of the ultrafiltration step were quantified.
Species production after each step was quantified using gas-chromatography techniques.
A combined treatment was designed for lowering the leaching of contaminants and the effect of each treatment step was quantified.
Each optimization step was quantified and the ligand binding active fraction of the receptor samples could drastically be improved.
The saturated functionalized dye density by a single step was quantified at 2.25 × 1014 molecules/cm2 on glassy carbon by dye assay, the same as that of two-step functionalization.
The next step is quantifying the asphaltene precipitation tendency in the precipitation zone.
The microRNAs obtained from one-step and two-step centrifugations were quantified by microarray and TaqMan-based real-time quantitative polymerase chain reaction (Q-PCR).
To address this question, two- and one-step functionalizations were quantified using dye assay on glassy carbon due to its well-defined area and similar chemical reactivity to CNTs.
For reasons of practicality, five stepped sections were quantified for all markers within Studies A and B. Exploration of the data for all transformed markers revealed them to be log-normally distributed.
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