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Cited by 317

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Adhesion Through Silane Coupling Agents

Plueddemann, Edwin P.·1970·The Journal of Adhesion

Abstract

From a study of silane coupling agents in reinforced plastics, a general mechanism of adhesion to hydrophilic mineral surfaces has been devised. According to this theory, adhesion of polymers to dissimilar surfaces is described as a dynamic equilibrium of making and breaking of adhesion bonds between polymer segments and the surface through the agency of a low molecular weight material—usually water. A dynamic equilibrium at the interface allows relaxation of thermal stresses. Water resistance results from a favorable equilibrium toward bonding through polar groups in the polymer. Silanol groups generally give optimum bonding to hydrophilic mineral surfaces.Such a dynamic mechanism of adhesion not only explains many complex adhesion problems of plastics to mineral surfaces, but also is compatible with the adhesion of ice, barnacles and tooth plaque to surfaces in an aqueous environment and with the requirements for rubber reinforcement by finely divided particulate fillers.

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Metadata

Authors
Plueddemann, E. P.
Venue
The Journal of Adhesion
Published
1970-07-01
Volume
2
Issue
3
Pages
184-201
ISSN
  • 0021-8464 (ISSN-L)
  • 1545-5823
OpenAlex
W2132323852
Cited by
317
References
1
FWCI
10.16
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Adhesion Through Silane Coupling Agents. https://app.cochat.ai/papers/10.1080/0021846708544592
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Plueddemann, E. P. (1970). Adhesion Through Silane Coupling Agents. The Journal of Adhesion. https://doi.org/10.1080/0021846708544592

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.