Sensor selection scheme is formulated as an Expected Value of Sample Information (EVSI) problem in the sequential Bayesian framework.
At last, the maximum ZT value of sample Co4Sb11.5Te0.5 prepared at 2.3 GPa reached 1.03 at 710 K due to its lower thermal conductivity and higher power factor.
We describe a novel process for transforming the efficiency of partial expected value of sample information (EVSI) computation in decision models.
This chart is able to detect two-sided mean shifts and increasing variance shifts by inspecting the absolute value of sample mean shift.
An analysis of the value of sample information was combined with dynamic programming and applied to numerical examples of sequential decision problems.
The onset of degradation temperature (Ti) value of sample containing 4 phr of CDs is 40 °C higher than the Ti value of neat XNBR latex.
In addition, the storage modulus (G′) value of sample containing 2 phr of CDs is 161% higher than the storage modulus value (G′) of neat XNBR latex.
The expected value of sample information (EVSI) from prospective trials has previously been modeled as the product of EVSI per patient, and the number of patients across the relevant time horizon less those "used up" in trials.
The subjective value of sample versus class is computed by the fuzzy computing theory, and the classified results obtained by self-organizing learning of Kohonen neural network are represented on output layer.
Engineering current density has been evaluated from direct measurement using a four-probe configuration, where best results have been reported for sample synthesized at 950 °C, with engineering current density of 3 × 105 atcm2 aT 2 T, almost two times the value of sample synthesized at 750 °C at the same field.
The optimized microextraction conditions were as follows: n-octanol was used as the extraction solvent, 0.09 M NaOH solution was used as acceptor phase, the pH value of sample solutions was 4.0, 30 g L−1 NaCl was solved in sample solutions, the stirring rate was 900 rpm and the extraction time was 60 min. The analysis of BPA was finished with injecting 20 μL acceptor phase by HPLC.
