1,721,003 research outputs found
Adsorption of polyelectrolytes to like-charged substrates induced by multivalent counterions as exemplified by poly(styrene sulfonate) and silica
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Studying the role of surface chemistry on polyelectrolyte adsorption using gold-thiol self-assembled monolayer with optical reflectivity
No full textSelf-assembled monolayers of thiols on gold are employed to study the role of surface chemistry on adsorption of polyelectrolytes to solid substrates. The suitability of these substrates is demonstrated in optical reflectivity, which combines high sensitivity to the possibility to precisely control the hydrodynamic conditions at the solid/water interface. Therefore, this system allows the determination of both the adsorbed amount and the kinetics of adsorption. The behavior of two representative strong polyelectrolytes of opposite charge is discussed as a function of pH and of concentration of a monovalent electrolyte in aqueous solutions. The application of equivalent substrates with varying surface chemistry sheds light on the role of different energetic contributions driving polyelectrolyte adsorption
Polyelectrolyte adsorption, interparticle forces, and colloidal aggregation
No full textThis review summarizes the current understanding of adsorption of polyelectrolytes to oppositely charged solid substrates, the resulting interaction forces between such substrates, and consequences for colloidal particle aggregation. The following conclusions can be reached based on experimental findings. Polyelectrolytes adsorb to oppositely charged solid substrates irreversibly up to saturation, whereby loose and thin monolayers are formed. The adsorbed polyelectrolytes normally carry a substantial amount of charge, which leads to a charge reversal. Frequently, the adsorbed films are laterally heterogeneous. With increasing salt levels, the adsorbed mass increases leading to thicker and more homogeneous films. Interaction forces between surfaces coated with saturated polyelectrolyte layers are governed at low salt levels by repulsive electric double layer interactions, and particle suspensions are stable under these conditions. At appropriately high salt levels, the forces become attractive, principally due to van der Waals interactions, but eventually also through other forces, and suspensions become unstable. This situation can be rationalized with the classical theory of Derjaguin, Landau, Verwey, and Overbeek (DLVO). Due to the irreversible nature of the adsorption process, stable unsaturated layers form in colloidal particle suspensions at lower polyelectrolyte doses. An unsaturated polyelectrolyte layer can neutralize the overall particle surface charge. Away from the charge reversal point, electric double layer forces are dominant and particle suspensions are stable. As the charge reversal point is approached, attractive van der Waals forces become important, and particle suspensions become unstable. This behaviour is again in line with the DLVO theory, which may even apply quantitatively, provided the polyelectrolyte films are sufficiently laterally homogeneous. For heterogeneous films, additional attractive patch–charge interactions may become important. Depletion interactions may also lead to attractive forces and suspension destabilization, but such interactions become important only at high polyelectrolyte concentrations
Adsorbed Mass of Polymers on Self-Assembled Monolayers: Effect of Surface Chemistry and Polymer Charge
No full textThe
adsorbed mass of polymers on surfaces with different chemistry
is presented, and the related adsorption mechanism is discussed. Strong
and weak polyelectrolytes of negative and positive charge are studied,
as well as an uncharged polymer. Self-assembled monolayers of alkanethiols
on gold are used in reflectometry and quartz crystal microbalance
(QCM-D) experiments as adsorbing substrates bearing different terminal
moieties, namely, methyl, hydroxyl, carboxyl, and amine groups. The
various polymer-surface combinations allow the systematic investigation
of the role of surface chemistry and polymer charge on adsorbed amount.
Interactions of different nature and range drive polymer adsorption:
the measured adsorbed amounts reveal information about their relative
contribution. When electrostatic chain-surface attraction is present,
the largest adsorbed masses are observed. However, significant mass
is measured even when an electrostatic barrier to adsorption is present,
suggesting the importance of forces of nonelectrostatic origin, which
include both hydrophobic interactions and specific forces acting at
short distances. This mechanism results in large adsorbed amounts
for the adsorption of weak polyelectrolytes, and it is apparent especially
in the adsorption behavior of a neutral polymer
Going Beyond Counting First Authors in Author Co-citation Analysis
Full text linkThe present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
Variations on the Author
Full text link“Variations on the Author” discusses two of Eduardo Coutinho’s recent films (Um Dia na Vida, from 2010, and Últimas Conversas, posthumously released in 2015) and their contribution to the general question of documentary authorship. The director’s filmography is characterized by a consistent yet self-effacing form of authorial self-inscription: Coutinho often features as an interviewer that rather than express opinions propels discourses; an interviewer that is good at listening. This mode of self-inscription characterizes him as an author who is not expressive but who is nonetheless markedly present on the screen. In Um Dia na Vida, however, Coutinho is completely absent form the image, while Últimas Conversas, on the contrary, includes a confessional prologue that moves the director from the margins to the center of his films. This article examines the ways in which these works stand out in the filmography of a director who offers new insights into the notion of cinematic authorship
Appropriate Similarity Measures for Author Cocitation Analysis
Full text linkWe provide a number of new insights into the methodological discussion about author cocitation analysis. We first argue that the use of the Pearson correlation for measuring the similarity between authors’ cocitation profiles is not very satisfactory. We then discuss what kind of similarity measures may be used as an alternative to the Pearson correlation. We consider three similarity measures in particular. One is the well-known cosine. The other two similarity measures have not been used before in the bibliometric literature. Finally, we show by means of an example that our findings have a high practical relevance.information science;Pearson correlation;cosine;similarity measure;author cocitation analysis
Dispelling the Myths Behind First-author Citation Counts
Full text linkWe conducted a full-scale evaluative citation analysis study of scholars in the XML research field to explore just how different from each other author rankings resulting from different citation counting methods actually are, and to demonstrate the capability of emerging data and tools on the Web in supporting more realistic citation counting methods. Our results contest some common arguments for the continued
use of first-author citation counts in the evaluation of scholars, such as high correlations between author rankings by first-author citation counts and other citation
counting methods, and high costs of using more realistic citation counting methods that are not well-supported by the ISI databases. It is argued that increasingly available digital full text research papers make it possible for citation analysis studies to go beyond what the ISI databases have directly supported and to employ more
sophisticated methods
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