Computer simulations of a new toroidal-cylindrical ion trap mass analyzer

2016 ◽  
Vol 30 (20) ◽  
pp. 2271-2278 ◽  
Author(s):  
Quan Yu ◽  
Lijuan Tang ◽  
Kai Ni ◽  
Xiang Qian ◽  
Xiaohao Wang

2015 ◽  
Vol 2015 (1) ◽  
pp. 000197-000202
Author(s):  
Patrick Roman ◽  
Xudong Chen ◽  
W. Kinzy Jones ◽  
Ali Karbasi ◽  
C. Mike Newton ◽  
...  

A chip based mass spectrometer technology promises to offer smart-device autonomous microsystem chemical analysis capability for sample determination and process monitoring for multiple applications in a small low power instrument package. This project focuses on the development of cylindrical ion trap mass analyzer chips fabricated using 3D Additive Manufacturing and planar Low Temperature Co-Fired Ceramic thick film processes toward the realization of a chip based mass spectrometer microsystem. The cylindrical ion trap (CIT) is a mass analyzer comprised of planar electrodes and operates by trapping and ejecting sample ions based on their mass in an RF field. Because of its simplicity CITs may be easily miniaturized and connected in tandem to achieve multiplexing. Additive manufacturing materials and methods enable enhanced trap miniaturization through micro machining and electrode patterning methods, fast and cost effective prototyping, batch fabrication, and material formulation flexibility. The current design incorporates three parallel ceramic plate metalized electrodes making up a singular trap geometry in a 10mm2 ceramic chip, forming a mass analyzer of reduced size, mass, and power, with enhanced material robustness for extended range use and in harsh environments. Unique processes have been developed to produce these devices which include conformal metallization layers, adhesion layers, ceramic paste formulations, sacrificial supporting materials, and co-firing methods. Additionally, 3D printing brings a unique design and fabrication capability enabling novel structures, material blending and heterogeneous integration. With true digital control, the designs are easily scalable and shape agnostic.



2016 ◽  
Vol 13 (3) ◽  
pp. 113-120
Author(s):  
Patrick Roman ◽  
Xudong Chen ◽  
W. Kinzy Jones ◽  
A. Karbasi ◽  
C. Mike Newton ◽  
...  

The current computing power and network capabilities of handheld smart devices is helping to drive the development of new sensors, enabling the Internet of things. A chip-based mass spectrometer technology promises to offer a smart-device autonomous microsystem chemical analysis capability for sample determination and process monitoring for multiple applications in a small low-power instrument package. This project focuses on the development of cylindrical ion trap (CIT) mass analyzer chips fabricated using three-dimensional (3-D) additive manufacturing (AM) and planar low temperature cofired ceramic thick film processes for a chip-based mass spectrometer microsystem. The CIT is a mass analyzer composed of planar electrodes and operates by trapping and ejecting sample ions based on their mass in a radiofrequency field. Because of its simplicity, CITs may be easily miniaturized and connected in tandem to achieve multiplexing. AM materials and methods enable enhanced trap miniaturization through micromachining and electrode patterning methods, fast and cost-effective prototyping, batch fabrication, and material formulation flexibility. The current design incorporates three parallel ceramic plate metalized electrodes making up a singular trap geometry in a 10-mm2 ceramic chip, forming a mass analyzer of reduced size, mass, and power, with enhanced material robustness for extended range use and in harsh environments. Unique processes have been developed to produce these devices which include conformal metallization layers, adhesion layers, ceramic paste formulations, sacrificial supporting materials, and cofiring methods. Additionally, 3-D printing brings a unique design and fabrication capability enabling novel structures, material blending, and heterogeneous integration. With true digital control, the designs are easily scalable and shape agnostic.



Author(s):  
Fu-Xing XU ◽  
Liang WANG ◽  
Yuan-Yuan WANG ◽  
Chuan-Fan DING


2003 ◽  
Vol 230 (1) ◽  
pp. 25-31 ◽  
Author(s):  
Won-Wook Lee ◽  
Cha-Hwan Oh ◽  
Pill-Soo Kim ◽  
Mo Yang ◽  
Kyuseok Song


2005 ◽  
Vol 241 (2-3) ◽  
pp. 119-132 ◽  
Author(s):  
Guangxiang Wu ◽  
R. Graham Cooks ◽  
Zheng Ouyang


2015 ◽  
Vol 26 (12) ◽  
pp. 2115-2124 ◽  
Author(s):  
Dragan Nikolić ◽  
Stojan M. Madzunkov ◽  
Murray R. Darrach


Separations ◽  
2020 ◽  
Vol 7 (1) ◽  
pp. 3 ◽  
Author(s):  
Benigno José Sieira ◽  
Inmaculada Carpinteiro ◽  
Rosario Rodil ◽  
José Benito Quintana ◽  
Rafael Cela

An analytical method based on high-resolution quadrupole–time-of-flight (QToF) mass spectrometry has been developed as an alternative to the classical method, using a low-resolution ion trap (IT) analyzer to reduce interferences in N-nitrosamines determination. Extraction of the targeted compounds was performed by solid-phase extraction (SPE) following the United States Environmental Protection Agency (USEPA) -521 method. First, both electron impact (EI) and positive chemical ionization (PCI) using methane as ionization gas were compared, along with IT and QToF detection. Then, parameters such as limits of detection (LOD) and quantification (LOQ), linearity, and repeatability were assessed. The results showed that the QToF mass analyzer combined with PCI was the best system for the determination of the N-nitrosamines, with instrumental LOD and LOQ in the ranges of 0.2–4 and 0.6–11 ng mL−1, respectively, which translated into method LOD and LOQ in the ranges of 0.2–1.3 and 0.6–3.9 ng L−1, respectively. The analysis of real samples showed the presence of 6 of the N-nitrosamines in influent, effluent, and tap water. N-nitrosodimethylamine (NDMA) was quantified in all the analyzed samples at concentrations between 1 and 27 ng L−1. Moreover, four additional nitrosamines were found in tap and wastewater samples.



2003 ◽  
Vol 75 (21) ◽  
pp. 5656-5664 ◽  
Author(s):  
Amy M. Tabert ◽  
Jens Griep-Raming ◽  
Andrew J. Guymon ◽  
R. Graham Cooks


2017 ◽  
Vol 421 ◽  
pp. 95-103
Author(s):  
Ailin Li ◽  
Jessica M. Higgs ◽  
Daniel E. Austin


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