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Other than using infinite basis sets, two methods exist to eliminate the BSSE. In the chemical Hamiltonian approach (CHA), [4] [5] basis set mixing is prevented a priori, by replacing the conventional Hamiltonian with one in which all the projector-containing terms that would allow mixing have
Endomicroscopy is a technique for obtaining histology-like images from inside the human body in real-time, [1] [2] [3] a process known as ‘optical biopsy’. [ 4 ] [ 5 ] It generally refers to fluorescence confocal microscopy , although multi-photon microscopy and optical coherence tomography have also been adapted for endoscopic use.
The handbook was originally published in 1928 by the Chemical Rubber Company (now CRC Press) as a supplement (Mathematical Tables) to the CRC Handbook of Chemistry and Physics. Beginning with the 10th edition (1956), it was published as CRC Standard Mathematical Tables and kept this title up to the 29th edition (1991).
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Any non-linear differentiable function, (,), of two variables, and , can be expanded as + +. If we take the variance on both sides and use the formula [11] for the variance of a linear combination of variables (+) = + + (,), then we obtain | | + | | +, where is the standard deviation of the function , is the standard deviation of , is the standard deviation of and = is the ...
Confocal endoscopy, or confocal laser endomicroscopy (CLE), is a modern imaging technique that allows the examination of real-time microscopic and histological features inside the body. In the word "endomicroscopy", endo- means "within" and -skopein means "to view or observe".
It is defined by the following equation: = | | | | | | | |, where F is the so-called structure factor and the sum extends over all the reflections of X-rays measured and their calculated counterparts respectively. The structure factor is closely related to the intensity of the reflection it describes:
Standard addition involves adding known amounts of analyte to an unknown sample, a process known as spiking.By increasing the number of spikes, the analyst can extrapolate for the analyte concentration in the unknown that has not been spiked. [2]