Journal De Physique Ii最新文献

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Phase Separation in Polymer Solutions Induced by Shear 剪切诱导聚合物溶液中的相分离
Journal De Physique Ii Pub Date : 1997-02-01 DOI: 10.1051/JP2:1997126
A. Onuki, R. Yamamoto, T. Taniguchi
{"title":"Phase Separation in Polymer Solutions Induced by Shear","authors":"A. Onuki, R. Yamamoto, T. Taniguchi","doi":"10.1051/JP2:1997126","DOIUrl":"https://doi.org/10.1051/JP2:1997126","url":null,"abstract":"We numerically investigate nonlinear regimes of shear-induced phase separation in entangled polymer solutions. Use is made of a time-dependent Ginzburg-Landau model describing two fluid dynamics of polymer and solvent. As a new dynamic variable a conformation tensor is introduced to represent chain deformations. Above the coexistence curve a dynamical steady states is attained, where fluctuations are enhanced on various spatial scales. At relatively large shear elongated polymer-rich regions form a transient network supporting most of the stress. Because such a network is continuously deformed in shear flow, the shear stress and the normal stress difference exhibit large fluctuations.","PeriodicalId":14774,"journal":{"name":"Journal De Physique Ii","volume":"23 1","pages":"295-304"},"PeriodicalIF":0.0,"publicationDate":"1997-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74605200","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 28
Surfactant limited aggregation of hydrophobic molecules in water 表面活性剂限制了疏水分子在水中的聚集
Journal De Physique Ii Pub Date : 1997-02-01 DOI: 10.1051/JP2:1997128
Helene Lannibois, A. Hasmy, R. Botet, O. A. Chariol, B. Cabane
{"title":"Surfactant limited aggregation of hydrophobic molecules in water","authors":"Helene Lannibois, A. Hasmy, R. Botet, O. A. Chariol, B. Cabane","doi":"10.1051/JP2:1997128","DOIUrl":"https://doi.org/10.1051/JP2:1997128","url":null,"abstract":"The precipitation in water of hydrophobic molecules has been studied in presence of added surfactants. Amorphous particles grow through aggregation of clusters of hydrophobic molecules; the growth is terminated by adsorption of surfactant. The particle sizes vary according to the concentrations of hydrophobic molecules and of surfactant molecules. Two regimes have been found for the use of surfactant molecules: at low surfactant concentrations, an efficient regime where all surfactant molecules are adsorbed on the surfaces of the growing particles; at high surfactant concentrations, a wasteful regime, where excess surfactant molecules are left in water. Attempts to reduce the particle sizes by adding increasing amounts of surfactant become inefficient at some point where most of the added surfactant remains in water. These results are explained by a kinetic aggregation model which simulates the competition between aggregation of hydrophobic molecules and adsorption of surfactant. The results of experiments are well reproduced by simulations where aggregation is allowed to proceed unimpeded for a time T, and then adsorption of the surfactant starts. In these conditions, particle sizes are determined by the rate of aggregation and by the value of this time delay.","PeriodicalId":14774,"journal":{"name":"Journal De Physique Ii","volume":"55 1","pages":"319-342"},"PeriodicalIF":0.0,"publicationDate":"1997-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74828455","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 28
Simplified Mean Field Theory for Polyelectrolyte Phase Behaviour 多电解质相行为的简化平均场理论
Journal De Physique Ii Pub Date : 1997-02-01 DOI: 10.1051/JP2:1997129
P. B. Warren
{"title":"Simplified Mean Field Theory for Polyelectrolyte Phase Behaviour","authors":"P. B. Warren","doi":"10.1051/JP2:1997129","DOIUrl":"https://doi.org/10.1051/JP2:1997129","url":null,"abstract":"Simplified mean field theory for the phase behaviour of polyelectrolytes in solution is described in detail. It can be viewed as the polyelectrolyte analogue of Flory-Huggins theory. A basic model is analyzed, then extended to look at the effects of multivalent ions (specifically divalent coions), of distinguishable counterions, and of an ionization equilibrium between counterions and polyelectrolyte. Analytic transformation of the free energy to reduce the number of extensive variables facilitates the calculation of binodal curves, tielines, spinodal curves, and the spinodal instability directions. Typical salting out behaviour and salt partitioning are seen. Unexpectedly, a small region of three phase coexistence is found: it is examined in detail for the basic model. In addition, the mean field spinodal is found to be identical to that occurring in common applications of the random phase approximation, and to have an interpretation in terms of electrostatic excluded volume, including for the ionizable polyelectrolyte case where fluctuations in the ionization equilibrium give an additional contribution to the Debye-Huckel screening length. The reasons for this are elucidated in an Appendix.","PeriodicalId":14774,"journal":{"name":"Journal De Physique Ii","volume":"34 1","pages":"343-361"},"PeriodicalIF":0.0,"publicationDate":"1997-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81100067","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 21
Characterizing the Nature of the Smectic A–Smectic C and Smectic A–Smectic C* Transitions Smectic A-Smectic C和Smectic A-Smectic C*跃迁性质的表征
Journal De Physique Ii Pub Date : 1997-02-01 DOI: 10.1051/JP2:1997120
L. Benguigui, P. Martinoty
{"title":"Characterizing the Nature of the Smectic A–Smectic C and Smectic A–Smectic C* Transitions","authors":"L. Benguigui, P. Martinoty","doi":"10.1051/JP2:1997120","DOIUrl":"https://doi.org/10.1051/JP2:1997120","url":null,"abstract":"Nous donnons une explication du comportement critique (c-a-d. non-champ moyen) de la chaleur specifique, qui a ete observe recemment sur certains composes. Cette explication repose sur l'energie libre de Andereck et Swift qui introduit des termes couplant le parametre d'ordre avec la compression de couche et la densite. Nous montrons que le comportement de la chaleur specifique depend de l'intensite de ces couplages et que les comportements qui peuvent etre observes sont par suite de type champ moyen, gaussien ou 3DXY.","PeriodicalId":14774,"journal":{"name":"Journal De Physique Ii","volume":"25 1","pages":"225-228"},"PeriodicalIF":0.0,"publicationDate":"1997-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82841624","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Diffusion in the Micellar and Hexagonal Phases of the C12EO6/H2O Mixture: A Directional-Growth Study C12EO6/H2O混合物胶束相和六方相的扩散:一个方向生长研究
Journal De Physique Ii Pub Date : 1997-01-01 DOI: 10.1051/JP2:1997117
L. Sallen, P. Oswald, P. Sotta
{"title":"Diffusion in the Micellar and Hexagonal Phases of the C12EO6/H2O Mixture: A Directional-Growth Study","authors":"L. Sallen, P. Oswald, P. Sotta","doi":"10.1051/JP2:1997117","DOIUrl":"https://doi.org/10.1051/JP2:1997117","url":null,"abstract":"Nous avons etudie en croissance directionnelle l'instabilite de Mullins-Sekerka a l'interface entre la phase hexagonale H∞ et la phase micellaire du melange lyotrope C 12 EO 6 +eau. Nous avons d'abord travaille a la concentration azeotrope (50% de surfactant en poids). Lorsque le C 12 EO 6 est pur, le melange se comporte comme un corps pur et l'instabilite de Mullins-Sekerka disparait. Elle reapparait lorsque le savon se degrade par oxydation radicalaire a la lumiere et a la chaleur. Nous avons mesure en fonction de la concentration en impuretes et de l'orientation des colonnes moleculaires, la vitesse critique, la longueur d'onde et la vitesse de derive des cellules en croissance et en fusion. De ces donnees experimentales, nous avons deduit les trois coefficients de diffusion moyens des impuretes dans la phase micellaire (D L i ) et dans la phase hexagonale, parallelement (D∥ i ) et perpendiculairement (D⊥ i ) aux colonnes moleculaires. Nous nous sommes ensuite ecartes legerement de la concentration azeotrope en prenant soin d'eviter la degradation du surfactant. Des experiences analogues en croissance et en fusion nous ont permis de determiner les trois coefficients de diffusion D L , D∥ et D⊥ du champ de concentration en surfactant. Les valeurs trouvees different de celles obtenues pour les impuretes et sont comparees aux coefficients de diffusion individuels de l'eau et du C 12 EO 6 mesures par RMN. Enfin, nous avons mesure le coefficient cinetique d'attachement moleculaire a l'interface. Nous avons trouve que la cinetique est lineaire et symetrique en croissance et en fusion.","PeriodicalId":14774,"journal":{"name":"Journal De Physique Ii","volume":"12 1","pages":"107-138"},"PeriodicalIF":0.0,"publicationDate":"1997-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79614991","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
Lattice of passages connecting membranes 连接膜的通道晶格
Journal De Physique Ii Pub Date : 1997-01-01 DOI: 10.1051/JP2:1997112
T. Charitat, B. Fourcade
{"title":"Lattice of passages connecting membranes","authors":"T. Charitat, B. Fourcade","doi":"10.1051/JP2:1997112","DOIUrl":"https://doi.org/10.1051/JP2:1997112","url":null,"abstract":"Lattices of passages connecting membranes are frequently observed in a variety of membranous systems. i§~e study their elastic properties within the framework of the curvature energy. Our calculations apply to the vesicle case where the constraints of constant surface and volume determine the shape profile. We concentrate on the physically relevant case of periodic boundary conditions for each cell containing passages, where the lattice parameter is set by the Gaussian bending modulus. It is shown that lattices of passages lack in-plane shear rigidity and we propose this as the basic reason for the strong fluctuations which are observed in experiments. Other compression modes couple to the vesicle shape. Our calculations are based on a detailed analysis of the shape equation. Using the Abrikosov vortex solution we show the analogies between lattices of passages and topological defects.","PeriodicalId":14774,"journal":{"name":"Journal De Physique Ii","volume":"72 1","pages":"15-35"},"PeriodicalIF":0.0,"publicationDate":"1997-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77276140","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 17
Dynamics in blends of long polymers with unentangled short chains 无纠缠短链长聚合物共混物动力学
Journal De Physique Ii Pub Date : 1997-01-01 DOI: 10.1051/JP2:1997116
R. Colby
{"title":"Dynamics in blends of long polymers with unentangled short chains","authors":"R. Colby","doi":"10.1051/JP2:1997116","DOIUrl":"https://doi.org/10.1051/JP2:1997116","url":null,"abstract":"Scaling ideas for dynamics of polymer solutions are extended to the case of a solution of long chains (of N monomers) in unentangled short chains (of P monomers). The P chains can be sufficiently short to make the long chains partially swell (P p 2 ), hydrodynamic interactions control their terminal relaxation. When N < P 2 , excluded volume is fully screened, and the dilute long chains relax by Rouse motion (with hydrodynamic interactions fully screened). The assumptions about hydrodynamic screening in dilute solution have consequences in the semidilute regimes of unentangled and entangled behavior, where we calculate the viscosity and the tracer diffusion coefficients. We end with a discussion of assumptions about hydrodynamic screening, and experiments are suggested to test those assumptions using binary blends with one unentangled component.","PeriodicalId":14774,"journal":{"name":"Journal De Physique Ii","volume":"49 11 1","pages":"93-105"},"PeriodicalIF":0.0,"publicationDate":"1997-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73023380","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Thermodynamic Theory of Counterion Association in Rigid Polyelectrolytes 刚性聚电解质中反离子缔合的热力学理论
Journal De Physique Ii Pub Date : 1997-01-01 DOI: 10.1051/JP2:1997113
Y. Levin, M. Barbosa
{"title":"Thermodynamic Theory of Counterion Association in Rigid Polyelectrolytes","authors":"Y. Levin, M. Barbosa","doi":"10.1051/JP2:1997113","DOIUrl":"https://doi.org/10.1051/JP2:1997113","url":null,"abstract":"We present a new theory of rodlike polyelectrolyte solutions. It is found that at low densities, and below teInperature T~i, the counterions associate with the polyions forIn- ing clusters consisting of one polyion and n counterions. The distribution of du8ters sizes is Gaussian, leading to strong logarithmic corrections to the liIniting laws obtained by Manning. In the Inathelnatical limit of infinite dilution the distribution of the cluster sizes approaches a delta function centered on the value postulated by Manning. Above Tci the solution consists of free (unassociated) counterions and polyions, and the liIniting laws reInain unaffected. Finally, unlike soIne recent suggestions, we denlonstrate that the counterion condensation is distinct fron1the Kosterlitz-Thouless transition. In fact, the association phenoInena inside a polyelec- trolyte solution can be coInpared to a fornlation of nlicelles in anlphiphilic systenls. There is, however, an iInportant difference. While the aInphiphilic rnicelles can be diluted away (bro- ken apart) by increasing the aInount of 801vent, the strong electrostatic interactions keep the polyion-counterion8 clusters froIn dissociating, even a8 the concentration of polyelectrolyte is decrea8ed all the way down to zero.","PeriodicalId":14774,"journal":{"name":"Journal De Physique Ii","volume":"336 1","pages":"37-55"},"PeriodicalIF":0.0,"publicationDate":"1997-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73882447","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 10
IR-Modulation Spectroscopy on the Collective Dynamics of Free-Standing Ferroelectric Liquid Crystalline Films 独立铁电液晶膜集体动力学的红外调制光谱研究
Journal De Physique Ii Pub Date : 1997-01-01 DOI: 10.1051/JP2:1997114
N. Klöpper, F. Kremer, T. Fischer
{"title":"IR-Modulation Spectroscopy on the Collective Dynamics of Free-Standing Ferroelectric Liquid Crystalline Films","authors":"N. Klöpper, F. Kremer, T. Fischer","doi":"10.1051/JP2:1997114","DOIUrl":"https://doi.org/10.1051/JP2:1997114","url":null,"abstract":"We present a novel experimental approach for determining the dynamics of free-standing ferroelectric liquid crystalline films in the frequency range from 1 Hz to 10 3 Hz. By measuring the dynamic infrared dichroism of specific absorption bands in a free-standing FLC-film exposed to rotating external electric fields within a miniaturized electrode arrangement the collective dynamics and the innermolecular response of the FLC system can be analysed. In the SmC * phase a dynamic process is found which corresponds to a resonant switching behaviour which can be described by the model of kink switching. The main contribution to the dynamics of the SmC * phase is caused by the molecular moieties in the mesogenic core.","PeriodicalId":14774,"journal":{"name":"Journal De Physique Ii","volume":"34 1","pages":"57-67"},"PeriodicalIF":0.0,"publicationDate":"1997-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74912786","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Adsorption Study on DDAB Bilayers Using Contrast Variation with SANS 用对比变化法研究双分子膜对DDAB的吸附
Journal De Physique Ii Pub Date : 1997-01-01 DOI: 10.1051/JP2:1997110
F. Ricoul, M. Dubois, T. Zemb
{"title":"Adsorption Study on DDAB Bilayers Using Contrast Variation with SANS","authors":"F. Ricoul, M. Dubois, T. Zemb","doi":"10.1051/JP2:1997110","DOIUrl":"https://doi.org/10.1051/JP2:1997110","url":null,"abstract":"Partition coefficients of solutes between bilayers and water are determined with a new method, using contrast variation with SANS. The isotopic composition of the solvent that annuls the contrast is shown to depend on thermodynamical quantities related to the adsorption. Experimental results are given for two organic solute molecules (lactitol and aniline) in the favorable case of the swollen lamellar phase obtained with DDAB double chain surfactant.","PeriodicalId":14774,"journal":{"name":"Journal De Physique Ii","volume":"5 1","pages":"69-77"},"PeriodicalIF":0.0,"publicationDate":"1997-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80536739","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
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