Faculty Advisor

Kendra J. Adams

Faculty Advisor

Francisco Fernandez-Lima

Location

GC Ballrooms

Start Date

29-3-2017 2:00 PM

End Date

29-3-2017 4:00 PM

Session

Session 3

Session Topic

Poster

Abstract

Polychlorinated biphenyls (PCBs) are industrial pollutants classified as endocrine disruptors and can cause antagonistic effects in the reproductive, neurological, and immunity systems in humans and animals. The biological toxicity of PCBs depends on the position and number of chlorine atoms within the molecule, and they work to mimic or block essential hormones, causing significant health damages. In the present work, nine different congeners of hydroxylated PCBs (OH-PCBs), with varying number of chlorine atoms, were studied using trapped ion mobility coupled to mass spectrometry (TIMS-MS). In particular, isomers of OH-hepta-chlorinated biphenyls (e.g., 4-OH-PCB 187, 4-OH-PCB 172 and 3-OH-PCB 180) were analyzed individually and as a mixture, to evaluate the analytical power and capabilities of TIMS-MS. Ion-neutral collisional cross sections were determined experimentally and compared to candidate structures. Different strategies to separate molecular isomers are discussed.

Comments

**Abstract Only**

File Type

Poster

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Mar 29th, 2:00 PM Mar 29th, 4:00 PM

Analysis of Hydroxylated Polychlorinated Biphenyls using nESI-TIMS-MS

GC Ballrooms

Polychlorinated biphenyls (PCBs) are industrial pollutants classified as endocrine disruptors and can cause antagonistic effects in the reproductive, neurological, and immunity systems in humans and animals. The biological toxicity of PCBs depends on the position and number of chlorine atoms within the molecule, and they work to mimic or block essential hormones, causing significant health damages. In the present work, nine different congeners of hydroxylated PCBs (OH-PCBs), with varying number of chlorine atoms, were studied using trapped ion mobility coupled to mass spectrometry (TIMS-MS). In particular, isomers of OH-hepta-chlorinated biphenyls (e.g., 4-OH-PCB 187, 4-OH-PCB 172 and 3-OH-PCB 180) were analyzed individually and as a mixture, to evaluate the analytical power and capabilities of TIMS-MS. Ion-neutral collisional cross sections were determined experimentally and compared to candidate structures. Different strategies to separate molecular isomers are discussed.

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