Structural characterization of synthetic polymers using thermal-assisted atmospheric pressure glow discharge mass spectrometry.

Analyst

Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences and Beijing National Laboratory for Molecular Sciences, Beijing 100190, China.

Published: November 2012

With the development of material science and the practical needs of the polymer industry, rapid characterization of synthetic polymers using mass spectrometry is of sustainable interest. Herein a new method for characterizing synthetic polymers using thermal-assisted atmospheric pressure glow discharge mass spectrometry (TA-APGD-MS) is established. After illustration of the mechanism of ion formation, typical polymer samples such as polystyrene (PS), polyoxymethylene (POM) and poly (butanediol succinate) (PBS) were directly characterized at the molecular level using TA-APGD-MS. The thermal degradation products of synthetic polymers including monomer units and/or other fragments were rapidly detected by tandem mass spectrometry, providing rich information about the chemical composition for the structural characterization of homo- and co-polymers. The result suggests that TA-APGD-MS allows direct and rapid analysis of both synthetic homo-polymers and co-polymers under ambient conditions without any sample pretreatment. This method features high throughput, high sensitivity and rich information, showing promising applications in polymer science.

Download full-text PDF

Source
http://dx.doi.org/10.1039/c2an35770dDOI Listing

Publication Analysis

Top Keywords

synthetic polymers
16
mass spectrometry
16
structural characterization
8
characterization synthetic
8
polymers thermal-assisted
8
thermal-assisted atmospheric
8
atmospheric pressure
8
pressure glow
8
glow discharge
8
discharge mass
8

Similar Publications

Mechanical and Light Activation of Materials for Chemical Production.

Adv Mater

March 2025

Center for Bio-inspired Energy Science, Northwestern University, 2145 Sheridan Road, Evanston, IL, 60208, USA.

Mechanical expansion and contraction of pores within photosynthetic organisms regulate a series of processes that are necessary to manage light absorption, control gas exchange, and regulate water loss. These pores, known as stoma, allow the plant to maximize photosynthetic output depending on environmental conditions such as light intensity, humidity, and temperature by actively changing the size of the stomal opening. Despite advances in artificial photosynthetic systems, little is known about the effect of such mechanical actuation in synthetic materials where chemical reactions occur.

View Article and Find Full Text PDF

Development of biobased poly(urethanes--oxazolidones) organogels.

Soft Matter

March 2025

Department of Chemistry "Ugo Schiff" and CSGI, University of Florence, via della Lastruccia 3, Sesto Fiorentino, Florence, Italy.

Polyurethanes are largely employed in various fields such as building, insulation and adhesive industries, but there is the constant need to develop sustainable formulations using "green" components and feasible processes. Here, a new series of sustainable castor oil and epoxidized castor oil-based (CO/EpCO) polyurethane networks was synthetized and characterized. The added epoxy functions react with isocyanates forming oxazolidinone linkages in the gels' network, reducing the gelation time from over 3 hours up to 0.

View Article and Find Full Text PDF

Sustainable Biopolymer Colloids: Advances in Morphology for Enhanced Functionalities.

Langmuir

March 2025

Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina 27695, United States.

Biobased polymers such as cellulose, chitin/chitosan, starch, alginate, and lignin are making inroads as sustainable, environmentally safe and biodegradable alternatives to synthetic colloidal materials. This perspective summarizes recent developments in preparation techniques, identifies critical barriers, and proposes future directions for improving the performance and applicability of biopolymer colloidal structures. A major focus is the sustainable colloids morphology as a means of introducing functionality without chemical modification.

View Article and Find Full Text PDF

Creating artificial cells with a dynamic cytoskeleton, akin to those in living cells, is a major goal in bottom-up synthetic biology. In this study, we demonstrate the in situ polymerization of microtubules encapsulated in giant polymer-lipid hybrid vesicles (GHVs) composed of 1,2-dioleoyl-sn-glycero-3-phosphocholine and an amphiphilic block copolymer. The block copolymer is comprised of poly(cholesteryl methacrylate-co-butyl methacrylate) as the hydrophobic block and either poly(6-O-methacryloyl-D-galactopyranose) or poly(carboxyethyl acrylate) as the hydrophilic extension.

View Article and Find Full Text PDF

Two-Dimensional Heteropore Covalent Organic Frameworks: From Construction to Functions.

Acc Chem Res

March 2025

State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.

ConspectusCovalent organic frameworks (COFs) represent a fascinating class of crystalline porous polymers constructed from organic building blocks linked by covalent bonds. Benefiting from their high crystallinity, large surface area, and ease of functionalization, COFs have demonstrated significant potential across various fields, including gas adsorption, luminescence, sensing, catalysis, energy storage, nanomedicine, etc. In the first decade of COF development, only those with homogeneous porosity have been constructed, and thus, their topological structures are quite limited.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!