Polymer blends spectroscopy

Finally, similar effects can be seen in miscible polymer blends where the surface tension correlates with the enrichment of the lower-energy component at the surface as monitored by x-ray photoelectron spectroscopy [104],... 

As already indicated above, what one may consider a surface depends on the property under consideration. Adhesion is very much an outer atomic layer issue, unless one is dealing with materials like fibreboard in which the polymer resin may also be involved in mechanical anchoring onto the wood particles. Gloss and other optical properties are related to the penetration depth of optical radiation. The latter depends on the optical properties of the material, but in general involves more than a few micrometer thickness and therewith much more than the outer atomic layers only. It is thus the penetration depth of the probing technique that needs to be suitably selected with respect to the surface problem under investigation. Examples selected for various depths (< 10 nm, 10 s of nm, 100 nm, micrometer scale) have been presented in Chapter 10 of the book by Garton on Infrared Spectroscopy of Polymer Blends, Composites and Surfaces... 

Core damage frequency (CDF), for nuclear power facilities, 17 540 Coreless induction furnaces, 12 309-311 Core level electron energy loss spectroscopy (CEELS), 24 74 Coremans, Paul, 11 398 Core-shell model, 14 464 Core-shell particles, in polymer blends, 20 354-355... 

A. Garton, Infrared Spectroscopy of Polymer Blends, Composites and Surfaces, Hanser, Munich (1992)... 

The first data on polymer systems were collected via (laser-) light-scattering techniques [1] and turbidity measurements, further developed by Derham et al. [2,3]. Techniques based on the glass-transition of the polymer-blend constituents were also tested, such as DSC, Dynamic Mechanical Spectroscopy, and Dielectric relaxation [4]. Films made from solutions of... 

Compared to binary mixtures of low molecular fluids, the critical behavior of polymer blends has been much less explored so far. However, a number of interesting static and dynamic critical phenomena in polymer blends attract increasing attention [4, 5], Neutron, X-ray, and static light scattering experiments belong to the major techniques for characterizing the static properties of polymer blends. Photon correlation spectroscopy (PCS) has traditionally been the method of choice for the investigation of the dynamics of critical [6-9] and noncritical [10-12] polymer blends. 

Many studies use infrared spectroscopy for quality control and quality analysis in polymer production. It is particularly used for the determination of the composition of copolymers and polymer blends and also for determination of additive and filler contents [90, 91, 92]. 

The feasibility of diffuse reflectance NIR, Fourier transform mid-IR and FT-Raman spectroscopy in combination with multivariate data analysis for in/ on-line compositional analysis of binary polymer blends found in household and industrial recyclates has been reported [121, 122]. In addition, a thorough chemometric analysis of the Raman spectral data was performed. 

The ionic aggregates present in an ionomer act as physical crosslinks and drastically change the polymer properties. The blending of two ionomers enhances the compatibility via ion-ion interaction. The compatibilisation of polymer blends by specific ion-dipole and ion-ion interactions has recently received wide attention [93-96]. FT-IR spectroscopy is a powerful technique for investigating such specific interactions [97-99] in an ionic blend made from the acid form of sulfonated polystyrene and poly[(ethyl acrylate - CO (4, vinyl pyridine)]. Datta and co-workers [98] characterised blends of zinc oxide-neutralised maleated EPDM (m-EPDM) and zinc salt of an ethylene-methacrylic acid copolymer (Zn-EMA), wherein Zn-EMA content does not exceed 50% by weight. The blend behaves as an ionic thermoplastic elastomer (ITPE). Blends (Z0, Z5 and Z10) were prepared according to the following formulations [98] ... 

C NOE spectroscopy under MAS was used for probing polymer miscibility in polymer blends, polystyrene/polyvinyl methyl ether (PS/PVME) [42], This study takes advantage of the fact that crosspeaks appear only between spins that are neighbours of each other,... 

Another good example of using Raman spectroscopy in the polymer industry is to investigate polymer blends. Raman microimages have been used to investigate the spatial distributions of the components in a blend of brominated poly(isobutylene-co-para-methylstyrene (BIMS) and cis-1-4-polybutadiene (BR) containing silica, zinc stearate, thiate, and other additives (21). A Raman spectrum of a blend is shown in Fig. 7-33. Specific bands can be assigned to BIMS, BR, silica, and zinc stearate. A 10 x 10 xm contour... 

Keywords Focal Plane Array FTIR Imaging Infrared spectroscopy Polymer blends... 

Liu, J., Jean, Y.C., Yang, H. (1995) Free volume properties of polymer blends by positron annihilation spectroscopy Miscibility . Macromolecules. 28, 5774. 

Raman spectroscopy is sensitive to polymer conformation. For example, a polymer blend of polybutadiene-polystyrene in which polybutadiene is used to increase toughness of the polystyrene can be examined by Raman microscopy to identify its heterogeneity. Polybutadiene has three isomer conformations (cis-1,4, trans-1,4 and syndiotactic-1,2). These three types of isomers can be identified from C=C stretching modes as shown in Figure 9.36. The Raman spectra of the copolymer indicate the difference in amounts of isomer types at the edge and the center of the polybutadiene-polystyrene sample. Relative amounts of these isomer types affect the mechanical properties of the copolymer. 

The volume opens with an account of PISEMA Solid-State NMR Spectroscopy by A. Ramamoorthy, Y. Wei and D.-K. Lee, this is followed by a review of 3D Structure Elucidation Using NMR Chemical Shifts by U. Sternberg, R. Witter and A. S. Ulrich, next comes an account of Se NMR Spectroscopy and Its Applications in Chemistry by H. Duddeck, the following report is on Structural Studies of Polymer Blends by Solid State NMR from H. Kurosu and Q. Chen, finally there is a discussion of the Structural Characterization of Silicon-based Polymer Materials by Solid-State NMR Spectroscopy from S. Kuroki, H. Kimura and I. Ando. 

The effect of dissolved CO2 on the miscibility of polymer blends and on phase transitions of block copolymers has been measured with spectroscopy and scattering (40). The shifts in phase diagrams with CO2 pressure can be pronounced. Polymer blends may be trapped kinetically in metastable states before they have time to phase separate. Metastable polymer blends of polycarbonate (PC) and poly(styrene-cn-acrylonitiile) were formed with liquid and supercritical fluid CO2 in the PCA process, without the need for a surfactant. Because of the rapid mass transfer between the CO2 phase and the solution phase, the blends were trapped in a metastable state before they... 

A review of rheo-optical techniques by Sherman et al. (1996) notes that there has been an increase in the use of rheo-optic set-ups both for FT-IR dichroism and for dynamic IR dichroism spectroscopies for polymer melts and polymer blends. Skytt et al. (1996) highlight the use of simultaneous measurement of the transient or steady-state rheological properties and IR dichroism to characterize orientation in polymer melts. However, there is little reference to dual spectroscopic-rheological techniques for reactive polymer systems in the literature. 

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