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Pulse of polymers

The initial pulse of polymer solution which was injected into the column entry becomes diluted and attenuated as the different species are separated on the gel packing. The column effluent is monitored by detectors which respond to the weight concentration of polymer in the flowing eluant. The most common detector is a differential refractometer. Spectrophotometers, which operate at fixed frequencies, are also used as alternative or auxiliary detectors. Some special detectors which are needed particularly for branched polymers or copolymers are mentioned in Section 3.4.4. [Pg.104]

Corrections for instrumental broadening (also called axial dispersion) are also sometimes applied [15]. This phenomenon arises because of eddy diffusion and molecular diffusion at the leading and trailing edges of the pulse of polymer solution [16]. Hie result is a symmetrical, Gaussian spreading of the GPC... [Pg.105]

Subliming ablators are being used in a variety of manufacturing appHcations. The exposure of some organic polymers to pulsed uv-laser radiation results in spontaneous ablation by the sublimation of a controUed thickness of the material. This photoetching technique is utilized in the patterning of polymer films (40,41) (see PHOTOCHEMICAL TECHNOLOGY). [Pg.5]

The ramp of pressure to about 3 GPa observed in shock-loaded fused quartz has been used very effectively in acceleration-pulse loading studies of viscoelastic responses of polymers by Schuler and co-workers. The loading rates obtained at various thicknesses of fused quartz have been accurately characterized and data are summarized in Fig. 3.6. At higher peak pressures there are no precise standard materials to produce ramp loadings, but materials such as the ceramic pyroceram have been effectively employed. (See the description of the piezoelectric polymer in Chap. 5.)... [Pg.60]

Fig. 5.21. The shock-induced polarization of polymers as studied under impact loading is shown. For the current pulse shown, time increases from left to right. The increase of current in time is due to finite strain and dielectric constant change. (See Graham [79G01]). Fig. 5.21. The shock-induced polarization of polymers as studied under impact loading is shown. For the current pulse shown, time increases from left to right. The increase of current in time is due to finite strain and dielectric constant change. (See Graham [79G01]).
These observations were the basis for the proposal that polymers, like ionic crystals, exhibit shock-induced polarization due to mechanically induced defects which are forced into polar configurations with the large acceleration forces within the loading portion of the shock pulse. Such a process was termed a mechanically induced, bond-scission model [79G01] and is somewhat supported by independent observations of the propensity of polymers to be damaged by more conventional mechanical deformation processes. As in the ionic crystals, the mechanically induced, bond-scission model is an example of a catastrophic shock compression model. [Pg.133]

Ogasawara, Ma Application of Pulse Radiolysis to the Study of Polymers and Polymerizations. VoLlQ5,pp. 37-80,... [Pg.213]

Basic principles of modem NMR spectroscopy are the subject of many textbooks [167,188-196], including pulse techniques [197] for NMR of polymers, see Bodor [198]. A guide to multinuclear magnetic resonance is also available [199]. Several texts deal specifically with multidimensional NMR spectroscopy [169,197,200-202]. Ernst et al. [169] have reviewed the study of dynamic processes, such as chemical exchange... [Pg.330]

C 1-NMR spectroscopy is the method of choice for determining the molecular structure of polymers in solution [230]. Polyolefin 13C NMR is mainly quantitative ID 1-NMR multiple pulse techniques are used for spectral interpretation. The resolution obtained in 13C NMR spectra of LDPE is an order of magnitude larger than in the corresponding 1H-NMR spectra... [Pg.333]

In this chapter we illustrate a direct method of characterisation of polymer/additive dissolutions by means of (500 MHz) NMR, which takes advantage of selective signal suppression allowing elimination of unwanted signals, such as the ca. 105 x more intensive PE signal. The most effective approach to solvent suppression is the destruction of the net solvent magnetisation by pulsed... [Pg.697]

DJ Pinner, RH Friend, and N Tessler, Transient electroluminescence of polymer light emitting diodes using electrical pulses, J. Appl. Phys., 86 5116-5130, 1999. [Pg.41]

Solubility of polymers in tetramethyl ammonium hydroxide aqueous solution was measured by dipping the wafer on which the polymer solution was spin-coated, for 1 min. at 25°C. The prebake was carried out at 90°C for 5min. Sensitivity of resists was measured after the exposure with CA 800(Cobilt) or KrF excimer laser(0.9mJ/cm2/1 pulse). The polymer structure was determined by iH-NMR, 13C-NMR(FX90Q apparatus,JEOL) and 2 Si-NMR. The molecular weight distribution was determined with a Toyo Soda Model 801 gel permeation chromatograph at 40°C. The four columns were connected in series, each packed with G-2000H8x3 and G-400H8(Toyo Soda polystylene gel), respectively. [Pg.136]

The irradiation of a polymer surface with the high intensity, pulsed, fer-UV radiation of the excimer laser causes spontaneous vaporization of the excited volume. This phenomenon was first described by Srinivasan (1) and called ablative photodecomposition. The attention of many researchers was drawn to the exceptional capabilities of photoablation (2). Etching is confined to the irradiated volume, which can be microscopic or even of submicron dimensions, on heat-sensitive substrates like polymers. In most experimental conditions, there is no macroscopic evidence of thermal damage, even when small volumes are excited with pulses of... [Pg.411]

Electrical Conductivity. Measurements of the electrical conductivity of materials under Irradiation, particularly time-resolved conductivity following a pulse of electrons, can provide Information on mobilities and trapping mechanisms, free electron yield, and thermal1sat Ion times and path lengths. Some measurements have been done on polymers (45-47) particularly because of their technological Importance in the electronics Industry (37). More fundamental work Is needed. [Pg.22]


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See also in sourсe #XX -- [ Pg.232 , Pg.234 , Pg.314 ]




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Pulsed NMR of polymer rubbers and melts

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