Multicenter electric spraying ion source for micro liquid phase separation system and mass spectrum
An electrospray ion source and separation system technology, applied in the field of ion sources, can solve the problems of different ionization efficiency, inability to realize the combination of multiple liquid phase separation systems, and increase ionization efficiency, etc., and achieves strong versatility and practicability. , the structure is simple, the effect of increasing the ionization efficiency
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Embodiment 1
[0029] Such as figure 1Shown is a multi-channel electrospray ionization source coupled with a micro-liquid phase separation system and a mass spectrometer. A five-channel design is adopted, that is, the ion source 1 is composed of a heating capillary sleeve 2, a spray chamber 3, and five sockets 4 for installing a single-channel electrospray nozzle / nozzle distributed in a fan-shaped space. In addition, 5 is a nitrogen inlet, and 6 is a nitrogen outlet. Needles / nozzles suitable for different modes of separation systems coupled with mass spectrometers can be easily installed in 4, and the best spray effect can be achieved by adjusting the distance between the needles / nozzles and the inlet of the vacuum region of the mass spectrometer (heated capillary orifice). In this embodiment, ensure that the central axis of each single-channel electrospray nozzle / nozzle end intersects at the position of 0.8 cm from the front end of the vacuum zone inlet, so that the central axes of the fou...
Embodiment 2
[0035] Experimental conditions: capillary (Hebei Yongnian Ruifeng Chromatography Device Co., Ltd., inner diameter: 50 μm, outer diameter: 375 μm), syringe pump (Harvard, USA), LCQ duo Ion trap mass spectrometry (U.S. Finnigan company), the ion source used is the five-channel micro-liquid phase separation system described in embodiment 1 and the electrospray ion source coupled with mass spectrometry, the central axis of each single-channel electrospray nozzle / nozzle end Intersect at the position 0.6cm from the front end of the inlet of the vacuum area, so that the central axis of the end of the four single-channel electrospray nozzles / nozzles is at an angle of 45 degrees to the axis of the vacuum inlet, and the spray voltage is 2.2kV.
[0036] Sample: a polypeptide (m / z=815) (0.1% formic acid aqueous solution)
[0037] see image 3 , which is obtained by using a micro-liquid phase separation system provided in Example 1 of the present invention coupled with a mass spectrometer...
Embodiment 3
[0039] Experimental conditions: Michrom multidimensional liquid chromatography, LCQ duo Ion trap mass spectrometry (Finnigan, USA). The ion source used is the five-channel micro-liquid phase separation system described in Example 1 and the electrospray ion source coupled with mass spectrometry. The central axis of each single-channel electrospray nozzle / jet end intersects at the position of 1 cm from the front end of the vacuum zone inlet At the position, the central axes of the four single-channel electrospray needle / nozzle ends are at an angle of 45 degrees to the vacuum inlet axis, and the spray voltage is 3kV.
[0040] Liquid conditions: Chromatographic column: 250μm×50mm, 5μC18
[0041] Mobile phase: A: 2% ACN (containing 0.1% formic acid, 0.05% HFBA) B: 98% ACN (containing 0.1% formic acid, 0.05% HFBA); 60min gradient: 0min: 10%A; 50min: 40%; 55min: 60%A; 60min: 60%A; injection volume 2μL; flow rate 5μL / min.
[0042] Sample: 50μg / mL β-Casein hydrolyzate
[0043] see ...
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