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Electrospray ionization (ESI) is a technique used in mass spectrometry to produce ions using an electrospray in which a high voltage is applied to a liquid to create an aerosol. It is especially useful in producing ions from macromolecules because it overcomes the propensity of these molecules to fragment when ionized.
Probe electrospray ionization is an ambient ionization mass spectrometry technique developed by Kenzo Hiraoka et al. at the University of Yamanashi, Japan. [4] The technique was developed to address some of the issues associated with traditional electrospray ionization (ESI), including clogging of the capillary and contamination, whilst providing a means of rapid and direct sample analysis.
The original interface between capillary zone electrophoresis and mass spectrometry was developed in 1987 [9] by Richard D. Smith and coworkers at Pacific Northwest National Laboratory, and who also later were involved in development of interfaces with other CE variants, including capillary isotachophoresis and capillary isoelectric focusing.
A typical APCI source usually consists of three main parts: a sample inlet, a corona discharge needle, and an ion transfer region under intermediate pressure. [5] In the case of the heated nebulizer inlet [7] from an LC, as shown in the figure, the eluate flows at 0.2 to 2.0 mL/min into a pneumatic nebulizer which creates a mist of fine droplets.
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A syringe with a male luer lock fitting, and a needle with female luer lock fitting (purple) which screws into it. The Luer taper is a standardized system of small-scale fluid fittings used for making leak-free connections between a male-taper fitting and its mating female part on medical and laboratory instruments, including hypodermic syringe tips and needles or stopcocks and needles.
As previously stated, in FAB the samples are mixed with a non-volatile environment in order to be analyzed.FAB uses a liquid matrix that is mixed with the sample in order to provide a sample ion current that is sustained, reduces damages made to the sample by absorbing the impact of the primary beam, and keeps the sample molecules form aggregating. [8]
Pseudoelasticity is from the reversible motion of domain boundaries during the phase transformation, rather than just bond stretching or the introduction of defects in the crystal lattice (thus it is not true superelasticity but rather pseudoelasticity). Even if the domain boundaries do become pinned, they may be reversed through heating.