東華大學圖書館 |

語系: 繁體中文

說明(常見問題)

回圖書館首頁

手機版館藏查詢

登入

回首頁

切換: 標籤 | MARC模式 | ISBD

Development of Ultra-fast Modulation...

Bahaghighat, Daniel.

FindBook

Google Book

Amazon

博客來

Development of Ultra-fast Modulation for Application in Multi-dimensional Gas Chromatography.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Development of Ultra-fast Modulation for Application in Multi-dimensional Gas Chromatography./
作者:	Bahaghighat, Daniel.
出版者:	Ann Arbor : ProQuest Dissertations & Theses, : 2018,
面頁冊數:	170 p.
附註:	Source: Dissertations Abstracts International, Volume: 80-02, Section: B.
Contained By:	Dissertations Abstracts International80-02B.
標題:	Analytical chemistry. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10821631
ISBN:	9780438173927

Development of Ultra-fast Modulation for Application in Multi-dimensional Gas Chromatography.
Bahaghighat, Daniel.

Development of Ultra-fast Modulation for Application in Multi-dimensional Gas Chromatography. - Ann Arbor : ProQuest Dissertations & Theses, 2018 - 170 p.

Source: Dissertations Abstracts International, Volume: 80-02, Section: B.

Thesis (Ph.D.)--University of Washington, 2018.

This item must not be added to any third party search indexes.

A combination of four instrumental systems and one chemometric method are presented that improves the efficiency, resolving power (i.e. peak capacity/ peak capacity production), and lessens the typical time of multi-dimensional gas chromatography (MDGC) separation in a straightforward, easily interpretable manner. Application of partial modulation via a commercially available high speed pulse flow valve for two-dimensional gas chromatography (GCxGC) is shown to provide ultra-fast modulation with modulation periods ( PM) as short as 50 ms. This technique performs a combination of vacancy chromatography and frontal analysis by an injection of carrier gas at the union of the first column (1D) and second column (2D). Each pulse disturbance in the analyte concentration profile as it exits the first column (1D) results in vacancy like data that is readily converted into a second separation (2D). A three-step process converts the raw data into a format equivalent to a traditional GCxGC separation chromatogram: 1. signal differentiation, 2. inversion of data, 3. baseline correction. The first instrumental system (GCxGC-Flame Ionization Detector (FID) with a PM of 500 ms, separating a 115-component mixture composed of a wide range of boiling points (36-372 °C) compounds with apparent peak widths on the 2 D, 2Wb, ranged from 10 to 40 ms, producing a 2D peak capacity, 2 nc, of ~ 20, and the total peak capacity, n c,2D, was 7200 or a peak capacity production of 1200 peaks/min. For a PM of 75 ms, separating a low boiling point 15-component mixture isothermally, apparent peak widths on the 2D, 2Wb, averaged 10 ms producing a 2D peak capacity, 2nc, of ~ 7.5, with a peak capacity production of 950 peaks/min. The second system incorporated a high temperature diaphragm valve modulator and a pulse valve flow modulator to create a three-dimensional gas chromatography system (GC 3) with a peak capacity production of 1000 peaks/min which is a ~5 times increase in efficiency compared to other GC3 systems. The third instrumental design established capability with a time-of-flight mass spectrometer (TOF), a method was developed for GCxGC-TOF separation in which a concentration study was conducted with an 18-component mixture and a PM of 50 ms. The subsequent data was deconvoluted with multivariate curve resolution-alternating least squares (MCR-ALS) in order to obtain their identification via match values. The resulting MCR-ALS data was converted in a similar manner as before into GCxGC chromatograms. Lastly, the pulse valve flow modulator was demonstrated to conduct continuous gas sampling of a system via one dimensional (1D) chromatography. The method applies the partial modulation technique to create frontal analysis peaks that are then transformed into a 1D chromatogram of analytes from a dynamic system that present a novel method of continuous sampling.

ISBN: 9780438173927Subjects--Topical Terms:

3168300
Analytical chemistry.
Subjects--Index Terms:

Gas chromatography

Development of Ultra-fast Modulation for Application in Multi-dimensional Gas Chromatography.
LDR:04165nmm a2200361 4500 001 2267883
005 20200810100150.5
008 220629s2018 ||||||||||||||||| ||eng d
020 $a 9780438173927
035 $a (MiAaPQ)AAI10821631
035 $a (MiAaPQ)washington:18465
035 $a AAI10821631
040 $a MiAaPQ $c MiAaPQ
100 1 $a Bahaghighat, Daniel. $3 3545139
245 1 0 $a Development of Ultra-fast Modulation for Application in Multi-dimensional Gas Chromatography.
260 1 $a Ann Arbor : $b ProQuest Dissertations & Theses, $c 2018
300 $a 170 p.
500 $a Source: Dissertations Abstracts International, Volume: 80-02, Section: B.
500 $a Publisher info.: Dissertation/Thesis.
500 $a Advisor: Synovec, Robert E.
502 $a Thesis (Ph.D.)--University of Washington, 2018.
506 $a This item must not be added to any third party search indexes.
506 $a This item must not be sold to any third party vendors.
520 $a A combination of four instrumental systems and one chemometric method are presented that improves the efficiency, resolving power (i.e. peak capacity/ peak capacity production), and lessens the typical time of multi-dimensional gas chromatography (MDGC) separation in a straightforward, easily interpretable manner. Application of partial modulation via a commercially available high speed pulse flow valve for two-dimensional gas chromatography (GCxGC) is shown to provide ultra-fast modulation with modulation periods ( PM) as short as 50 ms. This technique performs a combination of vacancy chromatography and frontal analysis by an injection of carrier gas at the union of the first column (1D) and second column (2D). Each pulse disturbance in the analyte concentration profile as it exits the first column (1D) results in vacancy like data that is readily converted into a second separation (2D). A three-step process converts the raw data into a format equivalent to a traditional GCxGC separation chromatogram: 1. signal differentiation, 2. inversion of data, 3. baseline correction. The first instrumental system (GCxGC-Flame Ionization Detector (FID) with a PM of 500 ms, separating a 115-component mixture composed of a wide range of boiling points (36-372 °C) compounds with apparent peak widths on the 2 D, 2Wb, ranged from 10 to 40 ms, producing a 2D peak capacity, 2 nc, of ~ 20, and the total peak capacity, n c,2D, was 7200 or a peak capacity production of 1200 peaks/min. For a PM of 75 ms, separating a low boiling point 15-component mixture isothermally, apparent peak widths on the 2D, 2Wb, averaged 10 ms producing a 2D peak capacity, 2nc, of ~ 7.5, with a peak capacity production of 950 peaks/min. The second system incorporated a high temperature diaphragm valve modulator and a pulse valve flow modulator to create a three-dimensional gas chromatography system (GC 3) with a peak capacity production of 1000 peaks/min which is a ~5 times increase in efficiency compared to other GC3 systems. The third instrumental design established capability with a time-of-flight mass spectrometer (TOF), a method was developed for GCxGC-TOF separation in which a concentration study was conducted with an 18-component mixture and a PM of 50 ms. The subsequent data was deconvoluted with multivariate curve resolution-alternating least squares (MCR-ALS) in order to obtain their identification via match values. The resulting MCR-ALS data was converted in a similar manner as before into GCxGC chromatograms. Lastly, the pulse valve flow modulator was demonstrated to conduct continuous gas sampling of a system via one dimensional (1D) chromatography. The method applies the partial modulation technique to create frontal analysis peaks that are then transformed into a 1D chromatogram of analytes from a dynamic system that present a novel method of continuous sampling.
590 $a School code: 0250.
650 4 $a Analytical chemistry. $3 3168300
653 $a Gas chromatography
653 $a Modulation periods
653 $a Multidimentional gas chromatography
690 $a 0486
710 2 $a University of Washington. $b Chemistry. $3 2093573
773 0 $t Dissertations Abstracts International $g 80-02B.
790 $a 0250
791 $a Ph.D.
792 $a 2018
793 $a English
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10821631