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2 edition of Transient effects in diffusion controlled polymer cyclization. found in the catalog.

Transient effects in diffusion controlled polymer cyclization.

Hui-lin HsГј

Transient effects in diffusion controlled polymer cyclization.

by Hui-lin HsГј

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  • 29 Currently reading

Published .
Written in English


The Physical Object
Pagination82 leaves
Number of Pages82
ID Numbers
Open LibraryOL19470587M

The transport of small molecules (gases) in incompatible polymer blends, semi‐crystalline polymers, and filled polymer systems is usually examined in terms of transient sorption and permeation experiments which yield effective values of diffusivity and by: Polymer Synthesis (Advances in Polymer Science ()) Softcover reprint of the original 1st ed. Edition by R. Arshady (Author) ISBN ISBN Why is ISBN important? ISBN. This bar-code number lets you verify that you're getting exactly the right version or edition of a book. Format: Paperback.

Transient shear banding in entangled polymers: A study using the Rolie-Poly model J. M. Adams SEPNet and the Department of Physics, University of Surrey, Guildford GU2 7HX, United Kingdom S. M. Fielding Department of Physics, Durham University, Science Laboratories, South Road, Durham DH1 3LE, United Kingdom P. D. Olmsteda). Steric hindrance is a consequence of steric effects. Steric hindrance is the slowing of chemical reactions due to steric bulk. It is usually manifested in intermolecular reactions, whereas discussion of steric effects often focus on intramolecular hindrance is often exploited to control selectivity, such as slowing unwanted side-reactions.

Bowman, Christopher Distinguished Professor and the James M. and Catherine Patten Chair in Chemical Engineering Method for determining the kinetic parameters in diffusion-controlled free-radical homopolymerizations. Involves mass and energy balances for steady-state and transient reactor systems. Also covers residence time distribution. Books and Book Chapters (by year) 9. Microscopy, Mariamne Dehonor, Carlos Lόpez-Barrόn, and C. Macosko, Chapter 20 in Handbook of Polymer Synthesis, Characterization, and Processing, ed. Enrique Saldívar-Guerra and Eduardo Vivaldo-Lima, Pub. John Wiley File Size: KB.


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Transient effects in diffusion controlled polymer cyclization by Hui-lin HsГј Download PDF EPUB FB2

Transient effects in diffusion‐controlled polymer cyclization Article in Die Makromolekulare Chemie (6) - March with 5 Reads How we measure 'reads'. intramolecular excimer formation to the polymer cyclization rate. Shortly after, random labeling Also, the experimental significance of the transient effects of diffusion is unclear.

Often, the reaction mechanism is modified when a good fit cannot be The Pennsylvania State University. A combination of steady-state and fluorescence decay techniques permits one to measure the dynamics of end-to-end cyclization of a polymer chain subst Cited by: Cyclization of a Polymer: First-Passage Problem for a Non-Markovian Process contrary to e.g.

polymer cyclization which was considered we study the diffusion-controlled dynamics of a. The diffusion theory of adhesion is base on the adhesion strength of polymers to themselves (autohesion). Mutual diffusion (inter-diffusion) of macromolecules across the interface results in creating an inter-phase.

As a mechanism, mainly stated by Voyutskii [74] indicated that the macromolecular chains or chain segments are sufficiently moved and mutually soluble. The most important new feature is the introduction of software tools that enable automatic addition of links to Gold Book terms into text and HTML documents.

Release New major update to the online version of the Gold Book. Almost entries were either added or updated. Diffusion in polymer–solvent systems. Development of a unified framework for calculating molecular weight distribution in diffusion controlled free radical bulk homo-polymerization, Polymer, 46, 2, (), ().

Crossref. Ning Effects of polymer molecular weight and temperature on case II transport. Parham Sadooghi, Transient Coupled Radiation and Conduction Heat Transfer in a Scattering Layer of ARLEN, Polymer-Plastics Technology and Engineering, 45, 6, (), ().

Crossref Parham Sadooghi, Transient Thermal Effects of Radiant Energy In Semitransparent Materials, Journal of Thermophysics and Heat Transfer, 20, 3, (), (). It is due to the high steric-hindrance effect for the DMI monomer, which has long reactive branches on both sides of the vinyl DMI monomer, complicating the mechanisms of crystallization and cyclization and resulting in diminishing the contribution of high isotacticity to lower the barrier of cyclization by: 6.

Simulation of the Transient Behavior of Gels Based on an Analogy Between Diffusion and Heat Transfer The transient behaviors of the swelling and deswelling of gels involve concurrent mechanical deformation and solvent diffusion and exhibit a fascinating phenomenon.

In this paper, a simple numerical tool is developed by using an analogy between File Size: KB. The transient structural and rheological behavior of soft glassy materials out of equilibrium is studied under small, medium, and large amplitude oscillatory shearing and interpreted via the fully quantitative sequence of physical processes (SPP) by: 7.

Transient Instability in Case II Diffusion PATRICK GUIDOTTI, JOHN A. PELESKO fact, in many applications, such as in controlled release pharmaceuticals, the polymers utilized are very thin, suggesting that two-dimensional effects two-dimensional effects.

We begin by assuming that a polymer half-space is exposed to a reservoir. Ultrafast photochemical reactions in liquids occur on similar or shorter time scales compared to the equilibration of the optically populated excited state.

This equilibration involves the relaxation of intramolecular and/or solvent modes. As a consequence, the reaction dynamics are no longer exponential, cannot be quantified by rate constants, and may depend on the excitation wavelength Cited by: Publications Books.

Fredrickson, The Equilibrium Theory of Inhomogeneous Polymers (Oxford University Press, ; reissue with corrections in paperback, ). Journal Publications and Edited Book Contributions. We consider front formation and steady‐state front motion in a one‐dimensional polymer system undergoing case‐II diffusion.

The polymer system approximates a polymer sheet whose thickness is very small compared with its lateral dimensions. The osmotic pressure of Thomas and Windle (TW) is used in the theoretical analysis. The transient problem of front formation is by: /EVAL matrix systems are composed.

The results were analyzed using the pseudo-steady-diffusion models coupled with the fundamental concepts of percolation theory. The percolation thresholds for the two systems were calculated, which could indicate the contributions of pore diffusion and matrix : XU Tongwen He Binglin.

Pörschke, D. & Eigen, M. Co-operative non-enzymic base recognition. Kinetics of the helix–coil transition of the oligoribouridylic–oligoriboadenylic acid system and.

We study by extensive computer simulations the looping characteristics of linear polymers with varying persistence length inside a spherical cavity in the presence of macromolecular crowding.

For stiff chains, the looping probability and looping time reveal wildly oscillating patterns as functions of the chain length. The effects of crowding differ dramatically for flexible versus stiff by: The diffusion of low molar mass fullerenes in a crosslinked matrix of a conjugated polymer and the influence of crosslinking on the carrier mobility is discussed.

Finally, the use of crosslinking to make stable interlayers and the solution processing of multilayer OSCs are discussed in addition to presentation of a novel approach to stabilize.

Fast Track Communication Collective dynamics effect transient subdiffusion of inert tracers in flexible gel networks Aljaž Godec1,2, Maximilian Bauer1,3 and Ralf Metzler1,4 1Institute of Physics and Astronomy, University of Potsdam, Potsdam-Golm, Germany 2National Institute of Chemistry, Ljubljana, Slovenia 3Physics Department, Technical University of Munich, Garching, Germany.

Reversible Diels–Alder (DA) type networks were prepared from furan and maleimide monomers of different structure and functionality.

The factors controlling the dynamic network formation and their properties were discussed. Evolution of structure during both dynamic nonequilibrium and isothermal equilibrium network formation/breaking was followed by monitoring the modulus and conversion Author: Beata Strachota, Adama Morand, Jiří Dybal, Libor Matějka.A three-dimensional, transient model has been developed to study the transient dynamics of polymer electrolyte fuel cell (PEFC) operation.

First, various time constants are estimated for important transient phenomena of electrochemical double-layer discharging, gas transport through the gas diffusion layer (GDL) and membrane by: We propose a theoretical framework for dealing with a transient polymer network undergoing small deformations, based on the rate of breaking and reforming of network cross-links and the evolving elastic reference state.

In this framework, the characteristics of the deformed transient network at microscopic and macroscopic scales are naturally by: