Low dead volume integrated separation columns and Fabry-Pérot sensors for micro-gas chromatography

2013 ◽  
Author(s):  
Karthik Reddy ◽  
Jing Liu ◽  
Maung Kyaw Khaing Oo ◽  
Xudong Fan
Lab on a Chip ◽  
2013 ◽  
Vol 13 (5) ◽  
pp. 851 ◽  
Author(s):  
Jung Hwan Seo ◽  
Jing Liu ◽  
Xudong Fan ◽  
Katsuo Kurabayashi

1969 ◽  
Vol 52 (3) ◽  
pp. 541-545
Author(s):  
Laura Giuffrida ◽  
N Fred Ives

Abstract Microcoulometric gas chromatography has been available for many years for the specific determination of chlorine and sulfur in pesticides and other compounds. The less specific electron capture has been more widely used in many cases because of its higher sensitivity and also because it is decidedly easier to operate. For more functional microcoulometric equipment, changes have been made that simplify connections and reduce dead volume. The substitution of air as the carrier gas has been successful as well as practical. Additional aspects have been examined for optimum and efficient application of this system.


Sensors ◽  
2021 ◽  
Vol 21 (9) ◽  
pp. 3089
Author(s):  
Weilin Liao ◽  
Xiangyu Zhao ◽  
Hsueh-Tsung Lu ◽  
Tsenguun Byambadorj ◽  
Yutao Qin ◽  
...  

Gas chromatography is widely used to identify and quantify volatile organic compounds for applications ranging from environmental monitoring to homeland security. We investigate a new architecture for microfabricated gas chromatography systems that can significantly improve the range, speed, and efficiency of such systems. By using a cellular approach, it performs a partial separation of analytes even as the sampling is being performed. The subsequent separation step is then rapidly performed within each cell. The cells, each of which contains a preconcentrator and separation column, are arranged in progression of retentiveness. While accommodating a wide range of analytes, this progressive cellular architecture (PCA) also provides a pathway to improving energy efficiency and lifetime by reducing the need for heating the separation columns. As a proof of concept, a three-cell subsystem (PCA3mv) has been built; it incorporates a number of microfabricated components, including preconcentrators, separation columns, valves, connectors, and a carrier gas filter. The preconcentrator and separation column of each cell are monolithically implemented as a single chip that has a footprint of 1.8 × 5.2 cm2. This subsystem also incorporates two manifold arrays of microfabricated valves, each of which has a footprint of 1.3 × 1.4 cm2. Operated together with a commercial flame ionization detector, the subsystem has been tested against polar and nonpolar analytes (including alkanes, alcohols, aromatics, and phosphonate esters) over a molecular weight range of 32–212 g/mol and a vapor pressure range of 0.005–231 mmHg. The separations require an average column temperature of 63–68 °C within a duration of 12 min, and provide separation resolutions >2 for any two homologues that differ by one methyl group.


2011 ◽  
Vol 159 (1) ◽  
pp. 60-65 ◽  
Author(s):  
Karthik Reddy ◽  
Yunbo Guo ◽  
Jing Liu ◽  
Wonsuk Lee ◽  
Maung Kyaw Khaing Oo ◽  
...  

Sensors ◽  
2021 ◽  
Vol 21 (20) ◽  
pp. 6800
Author(s):  
Jizhou Hu ◽  
Hemi Qu ◽  
Wei Pang ◽  
Xuexin Duan

A microfluidic film bulk acoustic wave resonator gas sensor (mFBAR) adapted specifically as an in-line detector in gas chromatography was described. This miniaturized vapor sensor was a non-destructive detector with very low dead volume (0.02 μL). It was prepared by enclosing the resonator in a microfluidic channel on a chip with dimensions of only 15 mm × 15 mm × 1 mm. The device with polymer coating showed satisfactory performance in the detection of organophosphorus compound, demonstrating a very low detection limit (a dozen parts per billion) with relatively short response time (about fifteen seconds) toward the simulant of chemical warfare agent, dimethyl methylphosphonate. The in-line detection of the mFBAR sensor with FID was constructed and employed to directly measure the concentration profile on the solid surface by the mFBAR with the controlled concentration profile in the mobile phase at the same time. The difference of peak-maximum position between mobile phase and solid phase could be a convenient indicator to measure mass transfer rate. With the response of the mFBAR and FID obtained in one injection, an injection mass-independent parameter can be calculated and used to identify the analyte of interest.


2013 ◽  
Vol 22 (5) ◽  
pp. 1174-1179 ◽  
Author(s):  
Karthik Reddy ◽  
Jing Liu ◽  
Maung Kyaw Khaing Oo ◽  
Xudong Fan

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