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Process fallout quantifies how many defects a process produces and is measured by DPMO or PPM. Process yield is the complement of process fallout and is approximately equal to the area under the probability density function Φ ( σ ) = 1 2 π ∫ − σ σ e − t 2 / 2 d t {\displaystyle \Phi (\sigma )={\frac {1}{\sqrt {2\pi }}}\int _{-\sigma ...
The output of this measurement is often illustrated by a histogram and calculations that predict how many parts will be produced out of specification (OOS). Two parts of process capability are: Measure the variability of the output of a process, and; Compare that variability with a proposed specification or product tolerance
A carbon–carbon double bond consists of a sigma bond and a pi bond. This double bond is stronger than a single covalent bond (611 kJ/mol for C=C vs. 347 kJ/mol for C–C), [1] but not twice as strong. Double bonds are shorter than single bonds with an average bond length of 1.33 Å (133 pm) vs 1.53 Å for a typical C-C single bond. [7]
Crystallization of polymers is a process associated with partial alignment of their molecular chains. These chains fold together and form ordered regions called lamellae, which compose larger spheroidal structures named spherulites. [1] [2] Polymers can crystallize upon cooling from melting, mechanical stretching or solvent evaporation ...
Many of these in theory could decay through spontaneous fission, alpha decay, double beta decay, etc. with a very long half-life, but no radioactive decay has yet been observed. Thus, the number of stable nuclides is subject to change if some of these 251 are determined to be very long-lived radioactive nuclides in the future.
The failure rate of a six sigma distribution with the mean shifted 1.5 sigma is not equivalent to the failure rate of a 4.5 sigma process with the mean-centered on zero. [9] This allows for the fact that special causes may result in a deterioration in process performance over time and is designed to prevent underestimation of the defect levels ...
The main substrates of chymotrypsin are peptide bonds in which the amino acid N-terminal to the bond is a tryptophan, tyrosine, phenylalanine, or leucine. Like many proteases, chymotrypsin also hydrolyses amide bonds in vitro, a virtue that enabled the use of substrate analogs such as N-acetyl-L-phenylalanine p-nitrophenyl amide for enzyme assays.
Amino acid replacement is a change from one amino acid to a different amino acid in a protein due to point mutation in the corresponding DNA sequence. It is caused by nonsynonymous missense mutation which changes the codon sequence to code other amino acid instead of the original.