Sensors and Actuators B 195 (2014) 44–51
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Sensors and Actuators B: Chemical
jo u r nal homep age: www.elsevier.com/locate/snb
UV photo-ionization based asymmetric field differential ion mobility
sensor for trace gas detection
Suresh M.
a,∗
, Nilesh J. Vasa
a,1
, Vivek Agarwal
b
, Jacob Chandapillai
c,2
a
Department of Engineering Design, Indian Institute of Technology Madras, Chennai 600036, India
b
Department of Electrical Engineering, Indian Institute of Technology Bombay, Mumbai 400076, India
c
Fluid Control Research Institute, Kanjikode West, Palghat, Kerala 678623, India
a r t i c l e i n f o
Article history:
Received 25 July 2013
Received in revised form
21 December 2013
Accepted 3 January 2014
Available online 13 January 2014
Keywords:
Differential ion mobility
Asymmetric wave electric field
UV photo-ionization
Volatile organic compounds
Trace gas sensing
FA-IMS
a b s t r a c t
A high-field Asymmetric Waveform Ion Mobility Spectrometry (FA-IMS) with ultra-violet (UV) photo-
ionization source is proposed and demonstrated for measurement of trace amounts of volatile organic
compound (VOC) gases. Experimental studies performed with the sensor using a high frequency asym-
metrical waveform differential field for detection of acetone, hexane and acetone–hexane mixture in
trace concentrations are discussed. The detection limit as estimated for a signal-to-noise ratio of 3 is of
the order of 100 ppb for acetone and hexane. Experimental studies clearly show that selective sensing of
a gas in a mixture of gases is also possible by appropriate value for the compensation voltage. Numer-
ical Simulation is also performed using two-dimensional fluid-flow equations to estimate the motion
of ions in an electric field. The study also demonstrated influence of parameters such as flow velocity,
duty-ratio, on compensation voltage for detection of trace VOC gases with asymmetrical high-frequency
electric field. Results based on theoretical study are in agreement with the experimental studies.
© 2014 Elsevier B.V. All rights reserved.
1. Introduction
There is an increasing interest in study of patho-physiological
and metabolic processes in human body through compositional
analysis of human exhaled air [1–8]. Certain clusters of volatile
organic compounds (VOCs) in human breath are considered to serve
as non-invasive potential biomarkers for various disease states
such as hyper-lipidemia, cancer, diabetes, kidney and liver disease,
recent smoking behavior, etc. Techniques for trace gas detection,
such as Proton-Transfer Reaction Mass Spectrometry (PTR–MS) [6],
Gas Chromatography Mass Spectrometry (GC–MS) [5], Selected-
Ion Flow-tube Mass Spectrometry (SIFT–MS) [7], Tunable Diode
Laser Absorption Spectroscopy (TDLAS) [8], Cavity Ring-Down
Spectroscopy (CRDS) [8], have been reported for investigations
for human breath. A robust, compact, sensitive and economically
viable, with fast analysis and response is needed for widespread
and real-time analysis of trace gases. Some of laser based trace gas
sensing systems require special installation environments and are
not suited to large scale deployments. Recently, super-luminescent
diode with a wavelength in an optical communication band has
∗
Corresponding author. Tel.: +91 491 2566120; fax: +91 491 2566326.
E-mail address: mshere@gmail.com (S. M.).
1
Tel.: +91 44 22574706; fax: +91 44 22574732.
2
Tel.: +91 491 2566120; fax: +91 491 2566326.
been reported for NH
3
and H
2
O vapor measurements [9] based
on the absorption spectroscopy technique. The approach allows
detection of multiple gas species, but the wide range of VOCs
has specific absorption bands in the mid-infrared region (between
2 m and 5 m). On the other hand, Ion Mobility Spectrometry
(IMS) have been reported [10–20] for detection of trace VOCs for
chemical-biological applications. IMS methods have been based
on Time-of-flight (TOF) [11], ion-focusing aspiration based sensing
[12] or sensing based on differential mobility of ions in high and
low electric fields (FA-IMS) [13–20].
A typical TOF based ion mobility spectrometer (TOF-IMS) is com-
prised of an ionization source associated within an ion reaction
chamber, an ion drift chamber, an ion/molecule injection shutter
placed between the ion reaction chamber and the ion drift cham-
ber and an ion collector (Faraday plate). The separation of ions
requires an appreciable length of drift-tube to travel before they
are separated. The length of the drift tube used in IMS is typically
about 13–30 cm and the resolution of these instruments reduce if
the tube length is shortened. TOF-IMS chiefly relies on separation
of different ion species due to differing ion mobilities in an elec-
tric field applied longitudinally in direction of ion motion inside
the drift-tube. On the other hand in a FA-IMS sensor, separation
of ions is caused due to differential ion mobilities in high (a few
kV/cm to 10 kV/cm) and low fields when an asymmetric electric
field waveform (E
F
) of high frequency, typically 1–2 MHz, is applied
in a direction transverse to flow of ions [17–19]. During each cycle
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http://dx.doi.org/10.1016/j.snb.2014.01.008