Sentence examples for experimental quenching from inspiring English sources

Fitting the experimental quenching data for a chosen phospholipid to eq 1 gives the value of n for that phospholipid.

Our QM-MM based mechanism powerfully links structure to experimental quenching results, allowing, through Table 2, the highly plausible supposition that Trps 68 and 157 will exhibit a fast electron transfer deactivation of the excited state.

The simulation studies allowed a better understanding of experimental quench data and were used for determining the adequate dimensioning and protection of the highly stabilised superconducting cables for connecting magnets (busbars), optimising the quench heater strip layout for the main magnets, and studying quench back by induced eddy currents in the superconductor.

As pointed out by Dewing [52], the experimental procedure (quenching) used in [25] may have been a source of errors.

We predict essentially barrier-less photoelectron transfer (PET) from P3HT to the acceptor 2-[{7- 9,9-di-n-propyl-9H-fluoren-2-yl benzo[c] [1,2-[{7- 9,9-di-n-propyl-9H-fluoren-2-yl benzo[cor K12-[{7- 9,9-di-n-propyl-9H-fluoren-2-yl benzo[cnescence quenching efficiencies found for P3HT:K12-[{7- 9,9-di-n-propyl-9H-fluoren-2-yl benzo[c

Partitioning of many trace elements between aqueous fluids and melts or crystals can be determined by analyzing experimental products quenched from high-temperature and high-pressure (HTHP) conditions.

Overall objective of the project is to offer research institutions from the EU Member Countries and Associated States access to four large-scale experimental facilities QUENCH, LIVE, DISCO, and COMET.

The experimental Stern-Volmer quenching rate constant at room temperature and liquid nitrogen temperature were measured as (376±4)·10−3 μs−1 (x content/mol)−1 and (45±4)·10−3 μs−1 (x content/mol)−1 respectively.

After optimizing the experimental conditions, the quenching of chemiluminescence signal depended linearly on the concentration of HCG in the range of 0.1 mIU mL−1 10 mIU mL−1 and the detection limit was 0.06 mIU mL−1.

The migration and preferential segregation of a blend component in thin films demonstrated here are responsible for the great difference between in situ and ex situ experimental (not real quenching or annealing) results of polymer blend films, and help explain the slow kinetics of surface phase separation at early stage for blend thin films reported in literature.

Figure 6 represents an experimental curve of quenching variations.