Advanced polymeric materials: structure property relationships [Book Review]

2004 ◽  
Vol 20 (5) ◽  
pp. 43-44
Author(s):  
K.F. Schoch
Author(s):  
L. C. Sawyer

Structure-property relationships are important in the process optimization and fundamental understanding of many polymeric materials, including membranes. Polymer membranes are currently being used for separation, concentration or purification in a wide range of industrial process applications. The process used to manufacture the membrane, and the polymer type, determines the morphology, which influences the membrane transport properties and potential applications. The morphology includes: pore size, shape, distribution and their overall three dimensional arrangement. Microscopical methods are needed to image the structures formed by the various processes, in order to systematically study changes in variables for specific applications.


2002 ◽  
Vol 740 ◽  
Author(s):  
Li-Piin Sung ◽  
Stephanie Scierka ◽  
Mana Baghai-Anaraki ◽  
Derek L. Ho

ABSTRACTMetal-oxide nanoparticles can be used to optimize UV absorption and to enhance the stiffness, toughness, and probably the service life of polymeric materials. Characterization of the nano- and microstructure dispersion of particles is necessary to optimize the structure-property relationships. Characterizations of both TiO2 particles dispersed in an acrylic-urethane matrix and TiO2 nanostructured films obtained through sol-gel synthesis are discussed. Experimental methods include microscopy (confocal, AFM) and small angle neutron scattering (SANS). Results from SANS experiments, which yield information about the cluster size of the nano-TiO2 particles and the spatial dispersion in various nanoparticle/polymer samples are presented and compared to the results of microscopy studies.


2021 ◽  
Author(s):  
Hatice Kaplan Can ◽  
Serap Kavlak ◽  
Fatma Gurbuz ◽  
Mehmet Odabaşı

Abstract Extracellular polymeric substances (EPSs) can be defined as renewable, high molecular weight polymeric materials produced by bacteria and microorganisms. EPSs are composed of primarily polysaccharides and proteins, with minor amounts of nucleic acids, lipids, and humic substances. Cyanobacterial extracellular polymeric subtances have a significant physiological effect on bloom formation and stress tolerance in adverse conditions. Therefore, cyanobacterial EPS has an important factor for aquatic life, environment and human life. For these reasons, determining the structure and structure-property relationships of cyanobacterial EPS is important for understanding its behavior and performance. In this study, the identification of the structure-property relationships, thermal and viscoelastic properties of cyanobacterial extracellular polymeric substance, X-ray diffraction (XRD) analysis, differential thermal analysis (DTA) and dynamic mechanical analysis (DMA) have been performed. Viscoelastic properties of the polymeric materias have been interpreted by certain DMA parameters at a fixed frequency depending on the temperature to understand the performance of cyanobacterial EPS.


2019 ◽  
Vol 6 (3) ◽  
pp. 69 ◽  
Author(s):  
Aaron C. Wilson ◽  
Shih-Feng Chou ◽  
Roberto Lozano ◽  
Jonathan Y. Chen ◽  
Pierre F. Neuenschwander

Hemocompatibility remains a challenge for injectable and/or implantable medical devices, and thromboresistant coatings appear to be one of the most attractive methods to down-regulate the unwanted enzymatic reactions that promote the formation of blood clots. Among all polymeric materials, polyurethanes (PUs) are a class of biomaterials with excellent biocompatibility and bioinertness that are suitable for the use of thromboresistant coatings. In this work, we investigated the thermal and physico-mechanical behaviors of ester-based and ether-based PU films for potential uses in thromboresistant coatings. Our results show that poly(ester urethane) and poly(ether urethane) films exhibited characteristic peaks corresponding to their molecular configurations. Thermal characterizations suggest a two-step decomposition process for the poly(ether urethane) films. Physico-mechanical characterizations show that the surfaces of the PU films were hydrophobic with minimal weight changes in physiological conditions over 14 days. All PU films exhibited high tensile strength and large elongation to failure, attributed to their semi-crystalline structure. Finally, the in vitro clotting assays confirmed their thromboresistance with approximately 1000-fold increase in contact time with human blood plasma as compared to the glass control. Our work correlates the structure-property relationships of PU films with their excellent thromboresistant ability.


Materials ◽  
2021 ◽  
Vol 14 (15) ◽  
pp. 4236
Author(s):  
Ashanul Haque ◽  
Hani El Moll ◽  
Khalaf M. Alenezi ◽  
Muhammad S. Khan ◽  
Wai-Yeung Wong

Square planar organoplatinum(II) complexes have garnered immense interest in the area of materials research. The combination of the Pt(II) fragment with mono-, bi- tri- and tetradentate organic ligands gives rise to a large variety of complexes with intriguing properties, especially cyclometalated Pt(II) complexes in which ligands are connected through covalent bonds demonstrate higher stability, excellent photoluminescence properties, and diverse applications. The properties and applications of the Pt(II)-based materials can be smartly fine-tuned via a judicious selection of the cyclometalating as well as ancillary ligands. In this review, attempts have been made to provide a brief review of the recent developments of neutral Pt(II) organometallic complexes bearing bidentate cyclometalating ligands and β-diketonate ancillary ligands, i.e., (C^N)Pt(O^O) and (C^C)Pt(O^O) derivatives. Both small (monomeric, dimeric) and large (polymeric) materials have been considered. We critically assessed the role of functionalities (ligands) on photophysical properties and their impact on applications.


Author(s):  
J. Petermann ◽  
G. Broza ◽  
U. Rieck ◽  
A. Jaballah ◽  
A. Kawaguchi

Oriented overgrowth of polymer materials onto ionic crystals is well known and recently it was demonstrated that this epitaxial crystallisation can also occur in polymer/polymer systems, under certain conditions. The morphologies and the resulting physical properties of such systems will be presented, especially the influence of epitaxial interfaces on the adhesion of polymer laminates and the mechanical properties of epitaxially crystallized sandwiched layers.Materials used were polyethylene, PE, Lupolen 6021 DX (HDPE) and 1810 D (LDPE) from BASF AG; polypropylene, PP, (PPN) provided by Höchst AG and polybutene-1, PB-1, Vestolen BT from Chemische Werke Hüls. Thin oriented films were prepared according to the method of Petermann and Gohil, by winding up two different polymer films from two separately heated glass-plates simultaneously with the help of a motor driven cylinder. One double layer was used for TEM investigations, while about 1000 sandwiched layers were taken for mechanical tests.


Author(s):  
Barbara A. Wood

A controversial topic in the study of structure-property relationships of toughened polymer systems is the internal cavitation of toughener particles resulting from damage on impact or tensile deformation.Detailed observations of the influence of morphological characteristics such as particle size distribution on deformation mechanisms such as shear yield and cavitation could provide valuable guidance for selection of processing conditions, but TEM observation of damaged zones presents some experimental difficulties.Previously published TEM images of impact fractured toughened nylon show holes but contrast between matrix and toughener is lacking; other systems investigated have clearly shown cavitated impact modifier particles. In rubber toughened nylon, the physical characteristics of cavitated material differ from undamaged material to the extent that sectioning of heavily damaged regions by cryoultramicrotomy with a diamond knife results in sections of greater than optimum thickness (Figure 1). The detailed morphology is obscured despite selective staining of the rubber phase using the ruthenium trichloride route to ruthenium tetroxide.


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