TY - JOUR
T1 - Development and Application of a Novel Multiloop Splitter-Based Non-cryogenic Artificial Trapping Modulation System in Comprehensive Two-Dimensional Gas Chromatography
AU - Tungkijanansin, Nuttanee
AU - Nolvachai, Yada
AU - Varanusupakul, Puttaruksa
AU - Hinchiranan, Napida
AU - Kulsing, Chadin
AU - Marriott, Philip J.
N1 - Funding Information:
This research project was supported by the Second Century Fund (C2F), Chulalongkorn University. This research was also funded by the Thailand Science Research and Innovation Fund Chulalongkorn University CU_FRB65_food (16)_124_23_54, the 90th anniversary of the Chulalongkorn University fund, Ratchadapisek Sompoch Endowment Fund (2021), 764002-HE02, and the Researcher assistant fellowship of Chulalongkorn University. Single piece design was supported by Amani Corporation Limited, Thailand.
Publisher Copyright:
© 2023 American Chemical Society.
PY - 2023/6/27
Y1 - 2023/6/27
N2 - A multiloop splitter-based non-cryogenic artificial trapping (M-SNAT) modulation technique was established, which applied the first (1D) nonpolar and the second (2D) polar columns, deactivated fused silica (DFS) columns, a microfluidic Deans switch (DS), and splitters located between the 1D column outlet and the DS. The splitters were connected into multiple loops with a progressively doubled perimeter of the next loop. This enabled a duplex splitting mechanism within each loop consisting of splitting of analyte pulses, the pulse delay, and their combination which led to equally split peaks of the same analytes with the number of split peaks (nsplit) equal to 2m (m = number of loops). This system resulted in local profiles of artificially split-and-trapped analytes prior to their selective transfers onto the 2D column by means of periodic multiple heart-cuts (H/C). The developed SNAT approach can be successful, providing that the ratio of modulation period to sampling time (PM/tsamp) is equal to nsplit. The approach with nsplit = 16 was further developed into a single device platform and applied for the modulation of a wide range of compounds in waste tire pyrolysis samples with the RSD of ≤0.01 and <10% for the one-dimensional modulated peak times and peak areas, respectively (n = 50). The method enabled an artificial modulation mechanism without cryogen consumption and enhanced the 2D peak capacity (2nc) and 2D separation by use of a longer 2D column.
AB - A multiloop splitter-based non-cryogenic artificial trapping (M-SNAT) modulation technique was established, which applied the first (1D) nonpolar and the second (2D) polar columns, deactivated fused silica (DFS) columns, a microfluidic Deans switch (DS), and splitters located between the 1D column outlet and the DS. The splitters were connected into multiple loops with a progressively doubled perimeter of the next loop. This enabled a duplex splitting mechanism within each loop consisting of splitting of analyte pulses, the pulse delay, and their combination which led to equally split peaks of the same analytes with the number of split peaks (nsplit) equal to 2m (m = number of loops). This system resulted in local profiles of artificially split-and-trapped analytes prior to their selective transfers onto the 2D column by means of periodic multiple heart-cuts (H/C). The developed SNAT approach can be successful, providing that the ratio of modulation period to sampling time (PM/tsamp) is equal to nsplit. The approach with nsplit = 16 was further developed into a single device platform and applied for the modulation of a wide range of compounds in waste tire pyrolysis samples with the RSD of ≤0.01 and <10% for the one-dimensional modulated peak times and peak areas, respectively (n = 50). The method enabled an artificial modulation mechanism without cryogen consumption and enhanced the 2D peak capacity (2nc) and 2D separation by use of a longer 2D column.
UR - http://www.scopus.com/inward/record.url?scp=85163738586&partnerID=8YFLogxK
U2 - 10.1021/acs.analchem.2c04710
DO - 10.1021/acs.analchem.2c04710
M3 - Article
AN - SCOPUS:85163738586
SN - 0003-2700
VL - 95
SP - 9437
EP - 9444
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 25
ER -