Search results for "Dynamic equilibrium"

showing 7 items of 87 documents

Forces Between Solid Surfaces Across Polymer Melts as Revealed by Atomic Force Microscopy

2007

Forces between solid surfaces across polymer melts are poorly understood despite their fundamental importance and their relevance for making composite materials. Such force measurements reveal information on the structure of polymers at surfaces and of confined polymers. Experiments with the atomic force microscope and polyisoprene (PI) confirmed theoretical predictions that no long‐range force should be present in thermodynamic equilibrium. In poly(dimethyl siloxane) (PDMS) repulsive forces are observed at high molar mass. We attribute this to the formation of an immobilized layer caused by a slow release of adsorbed segments enhanced by entanglement. In low molar mass PDMS attractive forc…

chemistry.chemical_classificationKelvin probe force microscopeMolar massMaterials scienceThermodynamic equilibriumSurface forceNanotechnologyGeneral ChemistryAdhesionPolymerCondensed Matter PhysicsEnd-groupAdsorptionchemistryChemical physicsGeneral Materials ScienceSoft Materials
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Connectivity defects enhance chain dynamics in supramolecular polymer model-network gels

2016

Supramolecular polymer networks exhibit twofold dynamics: that of their polymer chains and that of the transient bonds between them, which is further complexed when irregular network structures lead to local variation of both. A typical irregularity is imperfect network-chain connectivity. To assess the impact of that, we study the diffusion of three different types of tracer polymers in supramolecular model networks of four-arm star-shaped poly(ethylene glycol). First, we focus on tracers that carry three stickers and one fluorescent label at their four arms, thereby creating an inherent network connectivity defect in their vicinity. Second, we embed tracers that carry four stickers and fo…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsDynamics (mechanics)Supramolecular chemistryNanotechnology02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsLocal variation01 natural sciences0104 chemical sciencesSupramolecular polymerschemistryChain (algebraic topology)Chemical physicsMaterials ChemistryModel networkPhysical and Theoretical Chemistry0210 nano-technologyDynamic equilibriumJournal of Polymer Science Part B: Polymer Physics
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Natural gas hydrates vs. induced dysfunctions in the hydrocarbon extraction process

2021

Cantoned fluids in porous-permeable or fractured media of reservoirs have acquired during the geological time special properties. The fluids from the reservoir could be or not a mixture of reservoir water, liquid hydrocarbons and gaseous hydrocarbons. Considering if inside of a reservoir there are two types of substances like natural gas and reservoir water which may be in the form of vaporous than the condition of saturation of gases with water vaporous is fulfilled. This process is taking place due to thermodynamic equilibrium resulting the so-called gas humidity. This state corroborated with a certain chemical composition plus favourable values of pressure and temperature may be decisive…

chemistry.chemical_classificationPetroleum engineeringThermodynamic equilibriumbusiness.industryClathrate hydrateHumidityEngineering (General). Civil engineering (General)HydrocarbonchemistryNatural gasExtraction (military)TA1-2040Saturation (chemistry)businessChemical compositionMATEC Web of Conferences
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A kinetic study of the formation of smectic phases in novel liquid crystal ionogens

2013

[EN] A multi-rate non-isothermal kinetic analysis of the isotropic-melt to liquid crystalline phase transition of novel liquid crystalline ionogenic copolymers, LCIs, the 10-(4-methoxyazobenzene-4'-oxy)decyl methacrylate]-co-2-(acrylamido-2-methyl-1-propanesulfonic acid)s, 10-MeOAzB/AMPS, copolymers, has been performed by means of calorimetric experiments. An analytical methodology which includes the study of the phase transition rate parameter, the determination of the activation energies by using Kissinger and Flynn-Wall-Ozawa models, and the study of the phase transition kinetics by the use of the Avrami theory, has been applied. The formation of the mesophases from the isotropic state o…

chemistry.chemical_classificationPhase transitionSolucions polimèriquesMaterials sciencePolymers and PlasticsThermodynamic equilibriumOrganic ChemistryDifferential scanning calorimetry (DSC)Non-isothermal melt-crystallisation kinetic analysisGeneral Physics and AstronomyThermodynamicsActivation energyPolymerCiència dels materialsMethacrylateSide chain liquid crystal polymers (SCLCPs)CrystallographychemistryLiquid crystalPhase (matter)MAQUINAS Y MOTORES TERMICOSMaterials ChemistryCopolymerLiquid crystal ionogens (LCIs)European Polymer Journal
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Polymere ester von säuren des phosphors, 6. Ringöffnende polymerisation cyclischer phosphite und phosphonite durch michaelis-arbuzov-reaktion.–Theori…

1977

The hypothesis of Harwood and Patel, suggesting for the polymerization of 2-phenyl-1,3,2-dioxaphospholane a type of insertion reaction to explain the formation of ethylenediphosphinic ester structures besides the normal 2-hydroxyethyl(phenyl)phosphonic ester structures is extended to similar monomers and its theoretical consequences are examined. It is shown that in such a system mutual transformations between ω-hydroxyalkyl-P-acid and alkylenedi(P-acid)structures should occur, establishing a dynamic equilibrium and leading to a sort of azeotropic polymer, in which only one unique composition is kinetically stable. Equations relating to different kinetic parameters are deduced.

chemistry.chemical_classificationchemistry.chemical_compoundMonomerchemistryPolymerizationInsertion reactionPolymer chemistryOrganic chemistryPolymerDynamic equilibriumDie Makromolekulare Chemie
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Explicit proton transfer in classical molecular dynamics simulations.

2014

We present Hydrogen Dynamics (HYDYN), a method that allows explicit proton transfer in classical force field molecular dynamics simulations at thermodynamic equilibrium. HYDYN reproduces the characteristic properties of the excess proton in water, from the special pair dance, to the continuous fluctuation between the limiting Eigen and Zundel complexes, and the water reorientation beyond the first solvation layer. Advantages of HYDYN with respect to existing methods are computational efficiency, microscopic reversibility, and easy parameterization for any force field peerReviewed

proton transferHydrogenThermodynamic equilibriumforce fieldSolvationWaterchemistry.chemical_elementGeneral ChemistryLimitingMolecular Dynamics Simulationλ-dynamicsexcess protonForce field (chemistry)Computational MathematicsMicroscopic reversibilityMolecular dynamicschemistryComputational chemistryChemical physicsThermodynamicsmolekyylidynamiikkaMCProtonsta116
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Self-regulation mechanism of an ecosystem in a non-Gaussian fluctuation regime

1996

We study a dynamical model for an ecological network of many interacting species. We consider a Malthus-Verhulst type of self-regulation mechanism. In the framework of the mean field theory we study the nonlinear relaxation in three different cases: (a) towards the equilibrium state, (b) towards the absorbing barrier, (c) at the critical point. We obtain asymptotic behavior in all different cases for the time average of the process. The dynamical behavior of the system, in the limit of infinitely many interacting species, is investigated in the stability and instability conditions and theoretical results are compared with numerical simulations. \textcopyright{} 1996 The American Physical So…

symbols.namesakeNonlinear systemMean field theoryThermodynamic equilibriumCritical point (thermodynamics)GaussiansymbolsTime averageStatistical physicsInstabilityEcological networkMathematics
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