Amphiphilic Surface Active Triblock Copolymers with Mixed Hydrophobic and Hydrophilic Side Chains for Tuned Marine Fouling-Release Properties

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2010 ◽  
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Craig J. Weinman ◽  
John A. Finlay ◽  
Benjamin R. Fletcher ◽  
Marvin Y. Paik ◽  
...  
2011 ◽  
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Youngjin Cho ◽  
Harihara S. Sundaram ◽  
Craig J. Weinman ◽  
Marvin Y. Paik ◽  
Michael D. Dimitriou ◽  
...  

Langmuir ◽  
2009 ◽  
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pp. 12266-12274 ◽  
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John A. Finlay ◽  
Daewon Park ◽  
Marvin Y. Paik ◽  
Sitaraman Krishnan ◽  
...  

2008 ◽  
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Zhigang Chen ◽  
Bret Chisholm ◽  
Jongsoo Kim ◽  
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2010 ◽  
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Biofouling ◽  
2014 ◽  
Vol 30 (4) ◽  
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E. Martinelli ◽  
G. Galli ◽  
A. Glisenti ◽  
S. Mieszkin ◽  
...  

2017 ◽  
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A. Camós Noguer ◽  
S.M. Olsen ◽  
S. Hvilsted ◽  
S. Kiil

Biofouling ◽  
2020 ◽  
pp. 1-22
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Wenfa Yu ◽  
Robin Wanka ◽  
John A. Finlay ◽  
Jessica L. Clarke ◽  
Anthony S. Clare ◽  
...  

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Mohamed S. Selim ◽  
Sherif A. El‐Safty ◽  
Ahmed M. Azzam ◽  
Mohamed A. Shenashen ◽  
Maher A. El‐Sockary ◽  
...  

Coatings ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 153 ◽  
Author(s):  
Elisa Martinelli ◽  
Elisa Guazzelli ◽  
Antonella Glisenti ◽  
Giancarlo Galli

(Meth)acrylic terpolymers carrying siloxane (Si), fluoroalkyl (F) and ethoxylated (EG) side chains were synthesized with comparable molar compositions and different lengths of the Si and EG side chains, while the length of the fluorinated side chain was kept constant. Such terpolymers were used as surface-active modifiers of polydimethylsiloxane (PDMS)-based films with a loading of 4 wt%. The surface chemical compositions of both the films and the pristine terpolymers were determined by angle-resolved X-ray photoelectron spectroscopy (AR-XPS) at different photoemission angles. The terpolymer was effectively segregated to the polymer−air interface of the films independent of the length of the constituent side chains. However, the specific details of the film surface modification depended upon the chemical structure of the terpolymer itself. The exceptionally high enrichment in F chains at the surface caused the accumulation of EG chains at the surface as well. The response of the films to the water environment was also proven to strictly depend on the type of terpolymer contained. While terpolymers with shorter EG chains appeared not to be affected by immersion in water for seven days, those containing longer EG chains underwent a massive surface reconstruction.


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