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1

ANDREOZZI, ANDREA. « Fabrication of nanostructured materials using block copolymer based lithography ». Doctoral thesis, Università degli Studi di Milano-Bicocca, 2012. http://hdl.handle.net/10281/28333.

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The main objective of the PhD research activity carried out at MDM Laboratory was the growth and manipulation of nano-objects to be used as building blocks for the fabrication of new generation of nano-transistors, nano-memories and nano-emitters. The first part of the research activity was related to the development of reproducible and controlled protocols for the fabrication of polymeric soft masks for advanced lithographic applications using block copolymers. To this purpose hexagonally packed nanoporous polymeric thin films were fabricated using PS-b-PMMA block copolymers and accurately characterized. Special care was used to the functionalization of the sample surface prior to block copolymer thin film deposition. The effect of the self assembled monolayer of random copolymers conventionally used for surface neutralization was deeply investigated. In particular it was observed that different random copolymer thin films influence the window of thicknesses in which perpendicular orientation of the PMMA domains with respect to the underlying substrate occurs, as well as the characteristic dimensions of the final nanoporous polymeric mask. The possibility of combining “bottom up” self assembly of block copolymers with “top down” patterned templates was then explored to register the periodic domains of the self assembled block copolymer film with the underlying topographic structure. E-beam lithography was used to fabricate trenches in the SiO2 substrate before the deposition of the block copolymer thin films. The nanoporous polymeric mask fabricated during the first part of the research activity was then used as soft mask for patterning the underlying substrate in order to create nanoporous SiO2 hard masks as well as for the fabrication of ordered arrays of Silicon nanodots. The hexagonally packed nanopores of the polymeric mask were transferred to the underlying SiO2 by reactive ion etching. The effects of the etching parameters on the final characteristics of the nanoporous oxide were deeply investigated. The nanoporous SiO2 template was then used as a backbone for the fabrication of tunable nanoporous Al2O3 substrates by atomic layer deposition growth of thin films of Al2O3 on the SiO2 template. Progressive reduction of the pore size down to complete pore filling was obtained by properly adjusting the thickness of the Al2O3 film. This activity demonstrated the feasibility of fabricating periodic nanostructures surfaces with tunable dimensions well below the 20 nm limit. Moreover, since a large variety of oxide materials can be grown by atomic layer deposition, the proposed methodology provided a general approach for the synthesis of nanoporous oxide with accurate control of pore dimension, size distribution and pore frequency. Ordered arrays of Si nanocrystals were fabricated using the nanoporous polymeric film as a lithographic mask to control the formation of the nanodots. Two different approaches were pursued leading to different configurations where nanodots are embedded/deposited in/on the dielectric matrix. The first approach was based on ion beam synthesis and consisted in the implantation of Si ions into the nanostructured polymeric film to locally introduce the desired ion supersaturation in a limited nanosized area. After removal of the polymeric film, a thermal annealing led to the formation of nanocrystals at a depth depending on the ion energy. The second approach was the lift-off process that included material deposition by e-beam evaporation onto the nano-structured polymeric film and on the exposed substrate regions followed by the subsequent removal of the polymeric template and material excess by wet or dry etching. These arrays of semiconducting nanodots are suitable for the fabrication of Si nanocrystals non volatile memories or Si nanocrystals nanoemitters.
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2

Liu, Xiumin. « Mass Spectrometry and Tandem Mass Spectrometry Analysis of Polymers and Polymer-Protein Interactions ». University of Akron / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=akron1406838246.

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3

Gao, Yuan. « Characterization of polymers and supramolecular protein-polymer bioconjugates using mass spectrometry ». University of Akron / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=akron1619735971168192.

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4

Staudt, Byron Helmut. « Funktionelle Polymere mittels kontrollierter Polymerisationstechniken : Von der Massenspektrometrie endfunktionalisierter Polymere und den mechanischen Eigenschaften photovernetzbarer Blockcopolymere ». Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2019. http://hdl.handle.net/11858/00-1735-0000-002E-E585-F.

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5

Snyder, Savannah R. « PROBING STRUCTURE-PROPERTY RELATIONSHIPS OF STIMULI-RESPONSIVE POLYMERS BY MULTI-DIMENSIONAL MASS SPECTROMETRY ». University of Akron / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=akron1597353164970207.

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6

Gerislioglu, Selim. « Microstructure Characterization of Polymers and Polymer-Protein Bioconjugates by Hyphenated Mass Spectrometry ». University of Akron / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=akron1534269781343128.

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7

Jackson, Anthony Trevor. « Tandem mass spectrometry of polymeric materials ». Thesis, University of Warwick, 1995. http://wrap.warwick.ac.uk/44296/.

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Mass spectrometry and tandem mass spectrometry (MS/MS) has been employed to analyse peptides (<600 daltons), synthetic polymers of low molecular weight (<10,000 daltons) and a mixture of polymer additives (300-1200 daltons). Mass spectrometry experiments were performed on a four sector mass spectrometer, a tandem quadrupole mass spectrometer and a time-of-flight instrument. High and low energy collision induced dissociation (CID) spectra were obtained by means of a four sector mass spectrometer and a tandem quadrupole instrument respectively. Surface induced dissociation (SID) spectra of peptides were obtained by means of a four sector mass spectrometer with a modified collision cell in the third field free region. Sequence data were generated by SID from protonated and cationated precursor ions of all four peptides analysed. Furthermore, broad metastable ion peaks were observed in the spectra, arising from fragmentation of precursor ions in the field free region between the electric sector and the magnetic sector of the second mass spectrometer. Field desorption was a good ionisation technique for the generation of molecular weight information from the polymer additives used. High energy eID was found to be more applicable than low energy eID to the structural determination of polymer additives as characteristic ions were observed in the spectra. Mechanisms have been proposed for the generation of some of the fragment ions observed. Ultraviolet-matrix assisted laser desorptionlionisation spectra of synthetic polymers of low molecular weight (<10,000 daltons) were used to calculate molecular weight averages. Furthermore, end group information was also obtained from CID spectra of the same polymer samples. End group and structural information was also obtained from polystyrene and a substituted polystyrene by means of FD-MS/MS.
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8

Thomya, Panthida. « STRUCTURAL CHARACTERIZATION OF COMPLEX POLYMER SYSTEMS BY DEGRADATION / MASS SPECTROMETRY ». Akron, OH : University of Akron, 2006. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=akron1163969934.

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Thesis (Ph. D.)--University of Akron, Dept. of Chemistry, 2006.
"December, 2006." Title from electronic dissertation title page (viewed 04/24/2008). Advisor, Chrys Wesdemiotis; Committee members, Matthew P. Espe, Jun Hu, Wiley J. Youngs, Frank W. Harris; Department Chair, Kim C. Calvo; Dean of the College, Ronald F. Levant; Dean of the Graduate School, George R. Newkome. Includes bibliographical references.
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9

Alexander, Nicolas Edward. « Multidimensional Mass Spectrometry of Amphiphilic Systems ». University of Akron / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=akron1532773038466757.

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10

Katzenmeyer, Bryan C. « Interfacing Liquid Chromatography or Ion Mobility Separation with Mult-Dimensional Mass Spectrometry for the Structural Characterization of Polymeric Materials ». University of Akron / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=akron1367252830.

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11

Ferrari, Maria Chiara <1980&gt. « Mass transport in polymers ». Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2009. http://amsdottorato.unibo.it/1629/1/Ferrari_Maria_Chiara_Tesi.pdf.

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The study of mass transport in polymeric membranes has grown in importance due to its potential application in many processes such as separation of gases and vapors, packaging, controlled drug release. The diffusion of a low molecular weight species in a polymer is often accompanied by other phenomena like swelling, reactions, stresses, that have not been investigated in all their aspects yet. Furthermore, novel materials have been developed that include inorganic fillers, reactive functional groups or ions, that make the scenery even more complicated. The present work focused on the experimental study of systems where the diffusion is accompanied by other processes; suitable models were also developed to describe the particular circumstances in order to understand the underlying concepts and be able to design the performances of the material. The effect of solvent-induced deformation in polymeric films during sorption processes was studied since the dilation, especially in constrained membranes, can cause the development of stresses and therefore early failures of the material. The bending beam technique was used to test the effects of the dilation and the stress induced in the polymer by penetrant diffusion. A model based on the laminate theory was developed that accounts for the swelling and is able to predict the stress that raise in the material. The addition of inorganic fillers affects the transport properties of polymeric films. Mixed matrix membranes based on fluorinated, high free volume matrices show attractive performances for separation purposes but there is a need for deeper investigation of the selectivity properties towards gases and vapors. A new procedure based on the NELF model was tested on the experimental data; it allows to predict solubility of every penetrant on the basis of data for one vapor. The method has proved to be useful also for the determination of the diffusion coefficient and for an estimation of the permeability in the composite materials. Oxygen scavenging systems can overcome lack of barrier properties in common polymers that forbids their application in sensitive applications as food packaging. The final goal of obtaining a membrane almost impermeable to oxygen leads to experimental times out of reach. Hence, a simple model was developed in order to describe the transport of oxygen in a membrane with also reactive groups and analyze the experimental data collected on SBS copolymers that show attractive scavenging capacity. Furthermore, a model for predicting the oxygen barrier behavior of a film formed as a blend of OSP in a common packaging material was built, considering particles capable of reactions with oxygen embedded in a non-reactive matrix. Perfluorosulphonic acid ionomers (PFSI) are capturing attention due to a high thermal and chemical resistance coupled with very peculiar transport properties, that make them appropriate to be used in fuel cells. The possible effect of different formation procedure was studied together with the swelling due to water sorption since both water uptake and dilation can dramatically affect the fuel cells performances. The water diffusion and sorption was studied with a FTIR-ATR spectrometer that can give deeper information on the bonds between water molecules and the sulphonic hydrophilic groups and, therefore, on the microstructure of the hydrated ionomer.
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12

Ferrari, Maria Chiara <1980&gt. « Mass transport in polymers ». Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2009. http://amsdottorato.unibo.it/1629/.

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The study of mass transport in polymeric membranes has grown in importance due to its potential application in many processes such as separation of gases and vapors, packaging, controlled drug release. The diffusion of a low molecular weight species in a polymer is often accompanied by other phenomena like swelling, reactions, stresses, that have not been investigated in all their aspects yet. Furthermore, novel materials have been developed that include inorganic fillers, reactive functional groups or ions, that make the scenery even more complicated. The present work focused on the experimental study of systems where the diffusion is accompanied by other processes; suitable models were also developed to describe the particular circumstances in order to understand the underlying concepts and be able to design the performances of the material. The effect of solvent-induced deformation in polymeric films during sorption processes was studied since the dilation, especially in constrained membranes, can cause the development of stresses and therefore early failures of the material. The bending beam technique was used to test the effects of the dilation and the stress induced in the polymer by penetrant diffusion. A model based on the laminate theory was developed that accounts for the swelling and is able to predict the stress that raise in the material. The addition of inorganic fillers affects the transport properties of polymeric films. Mixed matrix membranes based on fluorinated, high free volume matrices show attractive performances for separation purposes but there is a need for deeper investigation of the selectivity properties towards gases and vapors. A new procedure based on the NELF model was tested on the experimental data; it allows to predict solubility of every penetrant on the basis of data for one vapor. The method has proved to be useful also for the determination of the diffusion coefficient and for an estimation of the permeability in the composite materials. Oxygen scavenging systems can overcome lack of barrier properties in common polymers that forbids their application in sensitive applications as food packaging. The final goal of obtaining a membrane almost impermeable to oxygen leads to experimental times out of reach. Hence, a simple model was developed in order to describe the transport of oxygen in a membrane with also reactive groups and analyze the experimental data collected on SBS copolymers that show attractive scavenging capacity. Furthermore, a model for predicting the oxygen barrier behavior of a film formed as a blend of OSP in a common packaging material was built, considering particles capable of reactions with oxygen embedded in a non-reactive matrix. Perfluorosulphonic acid ionomers (PFSI) are capturing attention due to a high thermal and chemical resistance coupled with very peculiar transport properties, that make them appropriate to be used in fuel cells. The possible effect of different formation procedure was studied together with the swelling due to water sorption since both water uptake and dilation can dramatically affect the fuel cells performances. The water diffusion and sorption was studied with a FTIR-ATR spectrometer that can give deeper information on the bonds between water molecules and the sulphonic hydrophilic groups and, therefore, on the microstructure of the hydrated ionomer.
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13

Lipowski, Brian M. « Phase Behavior of 12-Hydroxystearic Acid Gels ». University of Akron / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=akron1417628844.

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14

Hill, Jacob A. Hill. « SURFACE LAYER MATRIX-ASSISTED LASER DESORPTION IONIZATION TIME OF FLIGHT MASS SPECTROMETRY (SL-MALDI-TOF MS) ANALYSIS OF POLYMER BLEND SURFACE COMPOSITION ». University of Akron / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=akron1514479406062149.

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15

Callan, John Francis. « Low molecular mass and polymeric liquid crystals containing sulphur ». Thesis, Queen's University Belfast, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.301776.

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16

Scionti, Vincenzo. « Novel Applications of Mass Spectrometry on Synthetic Polymeric Materials ». University of Akron / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=akron1335149657.

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17

Chaicharoen, Kittisak. « Mass and Tandem Mass Spectrometric Studies on Synthetic Polymers ». University of Akron / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=akron1217533390.

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18

Casiano-Maldonado, Madalis. « Mass Spectrometry Techniques for the Characterization of Synthetic Polymers, Biopolymers, Biodegradation Products and Their Interactions ». University of Akron / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=akron1332962590.

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19

Mao, Jialin. « CHARACTERIZATION OF POLYMER ARCHITECTURES AND SEQUENCES BY MULTI-STAGE MASS SPECTROMETRY ». University of Akron / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=akron1554913939030297.

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20

Woodward, Mark Stanton. « Fundamental studies and instrumental methodology in the mass spectrometric analysis of low-mass polymeric systems ». Thesis, University of Warwick, 2001. http://wrap.warwick.ac.uk/3973/.

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The analysis of polymer systems is a crucial field in modern petrochemicals and also other sectors of the chemical industry. This analysis stretches from simple mass measurement, to sample identification and structural studies. Mass spectrometry is one of a number of analytical fields that are used to investigate such samples, but it has been shown to have certain limitations for the routine analysis of polymers. Chapter one discusses the development of mass spectrometry and the progression that has led to the development of the methods of sample ionisation and separation that are most used today. It also discusses the field of polymer analysis and the other analytical techniques that are applied to such investigations in industry. Chapter two details the instrumentation used in this study and also the nature of the main samples that were investigated. Chapter three covers analysis by the technique of matrix-assisted laser desorption / ionisation which is the major mass spectrometric method currently for polymer analysis. Details of work investigating sample preparation arc given leading into a larger discussion of the mass biases that arise in such polymer analysis and a rationalisation of their causes. Chapter four details investigations of polymer analysis using an electrospray source on a Fourier-transform ion cyclotron resonance instrument. The added complexity of charge states is discussed leading to further study of the mass and charge variations given by instrumental conditions. Chapter five presents a small body of work in the field of structural analysis by the technique of collision-induced dissociation. Work with buckministerfullerene and a range of ethoxylate polymers is given to demonstrate the capabilities of such analysis. Chapter six concludes the thesis with a discussion of the topics raised in the previous chapters and how they affect the use of mass spectrometry as a routine tool for the industrial analysis of polymeric systems.
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21

Zhu, Ming. « Mass transport in and through polymers ». Thesis, University of Oxford, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.423358.

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22

Lu, Kuan. « Optimization Of Sublimation Conditions for Surface Layer Matrix-assisted Laser Desorption Ionization Time of Flight Mass Spectrometry Imaging (SL-MALDI- Tof MSI) of Polymer Surfaces ». University of Akron / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=akron1524846943404769.

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23

Zhao, Xiayun. « Process planning for thick-film mask projection micro stereolithography ». Thesis, Atlanta, Ga. : Georgia Institute of Technology, 2009. http://hdl.handle.net/1853/28097.

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24

Dabney, David E. « Analysis of Synthetic Polymers by Mass Spectrometry and Tandem Mass Spectrometry ». University of Akron / OhioLINK, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=akron1259021862.

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25

O'Neill, Jason Michael. « Multidimensional Mass Spectrometry Studies on Amphiphilic Polymer Blends and Cross-Linked Networks ». University of Akron / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=akron1624375174939496.

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26

Lau, Richard Yiu-Ting. « Study of surfaces of semi-crystalline polymers by static time-of-flight secondary ion mass spectrometry / ». View abstract or full-text, 2010. http://library.ust.hk/cgi/db/thesis.pl?CBME%202010%20LAU.

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27

Ho, Chengter Ted. « An investigation of sink mark formation in compression molding of polymeric composites / ». The Ohio State University, 1993. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487841975356368.

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28

Harton, Shane Edward. « Investigation of Polymer Phase Behavior at Heterogeneous Polymer-Polymer Interfaces using Secondary Ion Mass Spectrometry ». NCSU, 2006. http://www.lib.ncsu.edu/theses/available/etd-03012006-131419/.

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Changes in the thermodynamic behavior of polymer blends from bulk to heterogeneous interfaces is investigated using secondary ion mass spectrometry (SIMS). The use of a magnetic sector spectrometer (CAMECA IMS-6f) is fully explored in order to determine the optimal conditions in which to probe polymer surfaces and heterogeneous interfaces using three bilayer film systems, namely polystyrene (PS) with poly(methyl methacrylate) (PMMA), poly(cyclohexyl methacrylate) (PCHMA) with PMMA, and PS with poly(2-vinylpyridine) (P2VP). Two primary ion beams have been employed, O2+ with detection of positive secondary ions, and Cs+ with detection of negative secondary ions. It was found that each polymer thin film system must be closely investigated in order to determine the optimal conditions for depth profiling using SIMS. Three types of systems were further investigated using SIMS.
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29

Guo, Kai. « Mass Spectrometry Characterization of Novel Synthetic Materials ». University of Akron / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=akron1410477329.

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30

Tayler, Paul John. « Pyrolysis-mass spectrometry studies of some synthetic polymers ». Thesis, University of Salford, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.328042.

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31

Cunningham, Paul John. « Characterisation of polymers using laser microprobe mass spectrometry ». Thesis, University of Cambridge, 1992. https://www.repository.cam.ac.uk/handle/1810/272246.

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32

Staton, JoAnna Christen II. « Heat and Mass Transfer Characteristics of Desiccant Polymers ». Thesis, Virginia Tech, 1998. http://hdl.handle.net/10919/9785.

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Desiccant-enhanced air conditioning equipment has exhibited both the capability to improve humidity control and the potential to save energy costs by lowering the latent energy requirement of the supply air stream. The resulting increasing popularity of desiccant-enhanced air conditioning systems has sparked new interest in the search for a better, more efficient desiccant material. The ultimate goal of this research was to develop a material that, when applied to an existing air-to-air heat exchanger, would achieve the necessary heat and mass transfer in a single process, thus transforming a sensible heat exchanger into a total enthalpy exchanger. This study focuses on the development and determination of appropriate polymeric desiccant materials for use in different heat and mass transfer applications. Various candidate materials were initially studied. It was decided that polyvinyl alcohol best met the pre-determined selection criteria. After the focus material was chosen, numerical models representing two heat and mass transfer applications were created. One-dimensional numerical models were developed for the performance studies of a rotary wheel total enthalpy exchanger. A two-dimensional numerical model was developed for the performance studies of a fixed plate total enthalpy exchanger as well. Material characterization tests were performed to collect material property information required by the numerical models. Sensible, latent, and total efficiencies gathered from both the rotary wheel total enthalpy exchanger and the fixed plate total enthalpy exchanger models indicate potential uses for some candidate polyvinyl alcohol materials.
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33

Rainer, Matthias. « Mass spectrometric identification of biomolecules employing synthetic polymers ». Saarbrücken VDM Verlag Dr. Müller, 2007. http://d-nb.info/989168468/04.

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34

Hearn, M. J. « Polymer surface studies by Secondary Ion Mass Spectrometry ». Thesis, De Montfort University, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.380743.

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35

Lin, Guangxin. « The application of multiple quantum MAS NMR to materials ». [S.l. : s.n.], 1999. http://deposit.ddb.de/cgi-bin/dokserv?idn=958600406.

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36

Roberts, Carol Ann. « Mass transfer from swollen polymers measured by projected fringes ». Thesis, Coventry University, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.335392.

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37

Wyatt, Mark Francis. « Analysis of acrylic polymers by MALDI-TOF mass spectrometry ». Thesis, Durham University, 2001. http://etheses.dur.ac.uk/3962/.

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Poly(methyl methacrylate) (PMMA) homopolymers synthesised using 'classical' anionic methods and subsequently studied by matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry (MALDI-TOF-MS) are discussed. Specifically, the attempts at different end-group functionalisation reactions, their varying degrees of success, and the characterisation of these functionalized polymers via MALDI are reported. Extra peaks were observed in the spectra of samples containing a tertiary amine end-group. A mechanism for the in situ elimination of H(_2)(g) involving these end-groups, which would fit the observations, is proposed. Two alternative, 'non-classical' routes to the desired materials were investigated, as difficulties in successfully performing capping reactions to give end functionalised PMMA were noted. The first method was a variation of standard anionic polymerisation that involved the use of lithium silanolates, which could be performed at a higher temperature than normal. The second was a controlled free-radical technique known as Reversible Addition-Fragmentation Chain Transfer (RAFT). A lack of control of the polymerisation to the desired degree was observed with the former method. A well-defined RAFT sample was observed to undergo in situ eliminadon also, for which a mechanism involving the dithioester end-group is proposed, and which is supported by MALDI-collision induced dissociation (CID) evidence. The synthesis of block copolymers of various compositions of MMA with r-butyl methacrylate (t-BMA) and hexyl methacrylate (HMA), along with their homopolymers, and their subsequent characterisation is reported. PHMA was analysed easily, in contrast to Pt-BMA. Only copolymers with a high PMMA content were analysed successfully and this has been rationalised in terms of the factors that affect cationisation. The characterisation of equimolar blends of various end-functionalised PMMA samples is reported also. Samples that favour the binding of a metal ion over protonation appear to have a higher ion yield. Once more, these observations are rationalised in terms of the factors that affect cationisation.
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38

Houseman, Jonathan. « Branched chains in poly(methyl methacrylate) polymerisations incorporating a polymeric chain transfer agent ». Thesis, Loughborough University, 2000. https://dspace.lboro.ac.uk/2134/34854.

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Branching in poly(methyl methacrylate) (PMMA) is produced by incorporating a pre-prepared polymeric chain transfer agent (PCTA) into a single stage radical polymerisation. Samples of PCTA having a range of transfer functionalities and molar masses were synthesised by modifying a methacrylate-based copolymer. Control of branching in PMMA has been studied as a function of transfer functionality and molar mass in the PCT A and a function of MMA and initiator concentrations in the MMA polymerisation. The branched samples of PMMA have been characterised by size exclusion chromatography (SEC) with multi-detectors to determine Mark–Houwink and other parameters to assess levels of branching. Some PCTA samples have been prepared with a UV chromophore to facilitate characterisation by SEC-UV.
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39

Whitson, Sara E. « The Development, Implementation and Application of Ambient Ionization Mass Spectrometry to Complex Polymeric Systems ». University of Akron / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=akron1226433768.

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40

Wu, Jiawei. « Physical Properties of Blends of Triblock Copolymer (SEBS) with Low Molar Mass Liquid Crystals ». University of Akron / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=akron1434368185.

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41

Mack, Min Jung [Verfasser]. « Synthese von Anthracen-funktionalisierten Polymeren und Photodimerisierungseffekte / Min Jung Mack ». Aachen : Shaker, 2005. http://d-nb.info/1186587563/34.

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42

Giguere, Marie-Soleil. « Sequencing synthetic copolymers using electrospray ionization mass spectrometry ». Thesis, University of Ottawa (Canada), 2003. http://hdl.handle.net/10393/26485.

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The dissociation of gas-phase synthetic homopolymers poly(butyl acrylate) (PBA), poly(methyl methacrylate) (PMMA) and poly(vinyl acetate) (PVAc) ionized by Li+ or Na+ was investigated by electrospray-ionization tandem mass spectrometry. Based on these results it was possible to use tandem mass spectrometry to sequence three copolymers produced by free radical polymerization (PBA/PVAc, PBA/PMMA and PMMA/PVAc). In the case of PVAc containing copolymers, tandem mass spectrometry yielded partial sequence information including the number of VAc monomers and consecutive BA or MMA monomers while the complete sequence (and mixture of sequences) could be deduced for PBA/PMMA. The poly(vinyl acetate) ions lose acetic acid molecules from the polymer side chain, and ultimately metal acetate, to form a polyene with a positive charge on the carbon backbone while PBA and PMMA fragment along the polymer backbone. An extensive study was made of the dissociation characteristic of PVAc. Collision-induced dissociation (CID) was performed at different center-of-mass collision energies to study the sequential appearance of the fragment ions. Molecular mechanics/molecular dynamics (MM/MD), Hartree-Fock, semi-empirical and density functional calculations were employed to model the lowest energy dissociation processes.
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43

Treufeld, Imre. « I. Polymer Films for High Temperature Capacitor ApplicationsII. Differential Electrochemical Mass Spectrometry ». Case Western Reserve University School of Graduate Studies / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=case1465503063.

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Argin, Emir. « Structural And Thermal Characterization Of Polymers Via Pyrolysis Mass Spectrometry ». Master's thesis, METU, 2005. http://etd.lib.metu.edu.tr/upload/12606680/index.pdf.

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In the first part of this study, the structtural and thermal characterization of electrochemically and chemically polymerized poly(paraphenylene vinylene), (PPV), have been investigated by direct pyrolysis mass spectrometry. Thermal characteristics, and degradation products of electrochemically prepared poly(paraphenylene vinylene). Pyrolysis study indicated that thermal decomposition of PPV occurs at least two steps. The first being due to the loss of supporting electrolyte present and the second being decomposition of the polymer backbone.In the second part of the study, direct insertion probe pyrolysis mass spectrometry (DIP-MS) technique was used to perform the thermal and the structural characterization of electrochemically synthesized polyaniline,PANI. The effect of dopant used (HCL, HNO3 and H2SO4) and synthesis period have been investigated. For all the samples studied, three main thermall degradation stages have been recorded
evolution of low molecular weight species, evolution of dopant based products and evolution of degradation products of polymer.
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Steinmann, Mark [Verfasser]. « Binding patterns in main-chain phosphorus-containing polymers / Mark Steinmann ». Mainz : Universitätsbibliothek Mainz, 2018. http://d-nb.info/1151159441/34.

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Sallam, Sahar. « MASS SPECTROMETRY METHODS FOR THE ANALYSIS OF POLYMERS AND BIOCONJUGATES ». University of Akron / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=akron1511882035662337.

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Wei, Benqian. « Characterization of supramolecular peptide-polymer bioconjugates using multistage tandem mass spectrometry ». University of Akron / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=akron1554221356363952.

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Hart-Smith, Gene On Chemistry Faculty of Science UNSW. « Mass spectrometric investigations into free radical polymerisation reaction mechanisms ». Awarded by:University of New South Wales. Chemistry, 2009. http://handle.unsw.edu.au/1959.4/44621.

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Contemporary mass spectrometry (MS) instrumentation featuring electrospray ionisation (ESI) or matrix-assisted laser desorption/ionisation (MALDI) ion sources were used to characterise the polymer distributions generated in various free radical polymerisations, allowing insights to be gained into the reaction mechanisms operating in these systems. In studying atom transfer radical polymerisation (ATRP) mediated star polymerisations of methyl acrylate (MA), ESI was found to be more effective in obtaining a comprehensive list of the distinct products present in the samples under investigation when compared to the employed MALDI technique. Furthermore, these studies showed that terminal Br losses observed at relatively high monomer to polymer conversions could be accounted for via mechanisms involving the acetone derived radicals (CH3)2??OH, ??H3 and ??H2COCH3. Through the use of ESI, it was found that for bulk polymerisations of MA and aqueous media polymerisations of N-isopropylacrylamide (NIPAAm) initiated using 60Co ??-irradiation and mediated via reversible addition-fragmentation chain transfer (RAFT), hydrogen radicals formed via the radiolysis of RAFT agent and/or monomer, and in the case of the NIPAAm system, water, are capable of initiating the polymerisations. In the NIPAAm polymerisations under scrutiny, it was also observed that hydroxyl radicals generated via the radiolysis of water may contribute towards the initiation process, and that propagating chains can potentially become terminated via trithiocarbonate cleavage reactions. By using ESI instruments to characterise oligomer samples produced via the free radical polymerisations of vinyl phosphonates, it was observed that chain propagations are initiated via activated monomer radicals, which likely form as a result of transfer reactions involving initiator fragments and vinyl phosphonate monomer units. Transfer to monomer reactions were suggested to limit chain growth in these systems, and evidence was also found for scission reactions involving alkoxy moieties which are formed via intramolecular methine carbon abstraction reactions. Characterisation of the polymer distributions generated in R-group approach RAFT MA star polymerisations using an ESI instrument allowed formation processes operating in acrylate star living/controlled radical polymerisations (CRPs) to be ascertained. Initiator fragment derived linear chains, ideal stars, star-star couples, and terminated star products formed as a result of disproportionation and combination reactions were detected. Evidence for mid-chain radical (MCR) derived reaction pathways was also observed; specifically, for termination reactions involving intermolecularly formed MCRs on both star arms and linear chains, and for re-propagation of intermolecularly formed MCRs on star arms.
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Leeson, Alistair M. « Time-of-flight secondary ion mass spectroscopy of polymer surfaces ». Thesis, University of Sheffield, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.268294.

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Rahlves, Maik [Verfasser]. « Integrated polymer photonics : fabrication, design, characterization and applications / Maik Rahlves ». Hannover : Technische Informationsbibliothek (TIB), 2017. http://d-nb.info/1170080790/34.

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