Evolution and Applications of Polymer Brush Hypersurface Photolithography

2021 ◽  
Author(s):  
Daniel Valles ◽  
Yerzhan Zholdassov ◽  
Adam Braunschweig

Hypersurface Photolithography (HP) is a printing method for fabricating structures and patterns composed of polymer brushes, and can be used to create patterns with complex topologies or for rapidly accelerating...

Small ◽  
2012 ◽  
Vol 8 (23) ◽  
pp. 3567-3567 ◽  
Author(s):  
Xuechang Zhou ◽  
Zhilu Liu ◽  
Zhuang Xie ◽  
Xuqing Liu ◽  
Zijian Zheng

2007 ◽  
Vol 1049 ◽  
Author(s):  
Jeffrey B. Sokoloff

AbstractIt is shown using a method based on the mean field theory of Miklavic Marcelja that it should be possible for osmotic pressure due to the counterions associated with the two polyelectrolyte polymer brush coated surfaces to support a reasonable load (i.e., about 105 Pa) with the brushes held sufficiently far apart to prevent entanglement of polymers belonging to the two brushes, thus avoiding what is likely to be the dominant mechanisms for static and dry friction.


Soft Matter ◽  
2021 ◽  
Author(s):  
Piotr Polanowski ◽  
Andrzej Sikorski

Monodisperse polymer brushes were studied by means of Monte Carlo simulations. A coarse-grained model of a polymer brush was designed in order and the Cooperative Motion Algorithm was employed to...


Polymers ◽  
2018 ◽  
Vol 10 (10) ◽  
pp. 1165 ◽  
Author(s):  
Tobias Mai ◽  
Karol Wolski ◽  
Agnieszka Puciul-Malinowska ◽  
Alexey Kopyshev ◽  
Ralph Gräf ◽  
...  

This article describes the synthesis of anionic polymer brushes and their mineralization with calcium phosphate. The brushes are based on poly(3-sulfopropyl methacrylate potassium salt) providing a highly charged polymer brush surface. Homogeneous brushes with reproducible thicknesses are obtained via surface-initiated atom transfer radical polymerization. Mineralization with doubly concentrated simulated body fluid yields polymer/inorganic hybrid films containing AB-Type carbonated hydroxyapatite (CHAP), a material resembling the inorganic component of bone. Moreover, growth experiments using Dictyostelium discoideum amoebae demonstrate that the mineral-free and the mineral-containing polymer brushes have a good biocompatibility suggesting their use as biocompatible surfaces in implantology or related fields.


2013 ◽  
Vol 791-793 ◽  
pp. 208-211 ◽  
Author(s):  
Xiao Meng Chu ◽  
Shao Jie Liu ◽  
Hui Jiao Yang ◽  
Feng Qing Zhao

This paper firstly summarized the latest research progress on the polymer brushes preparation by surface-initiated ARGET ATRP polymerization. It mainly includes the surface modifications of inorganic substrate (silicon dioxide and carbon nanotubes), and the organic substrate (cellulose and polymer microspheres). This method needs less catalyst and operates more easily, compared to the classical ATRP. Besides, it also has good polymerization controllability, and the polymer brushes have higher grafting density and molecular weight. Therefore, surface-initiated ARGET ATRP polymerization has become an effective method for modifying the surface of materials. Then, we prepared the polymer brush supported TEMPO by the surface-initiated ARGET ATRP and characterized.


2021 ◽  
Vol 54 (3) ◽  
Author(s):  
Isaac J. Gresham ◽  
Timothy J. Murdoch ◽  
Edwin C. Johnson ◽  
Hayden Robertson ◽  
Grant B. Webber ◽  
...  

Neutron reflectometry is the foremost technique for in situ determination of the volume fraction profiles of polymer brushes at planar interfaces. However, the subtle features in the reflectometry data produced by these diffuse interfaces challenge data interpretation. Historically, data analyses have used least-squares approaches that do not adequately quantify the uncertainty of the modeled profile and ignore the possibility of other structures that also match the collected data (multimodality). Here, a Bayesian statistical approach is used that permits the structural uncertainty and multimodality to be quantified for polymer brush systems. A free-form model is used to describe the volume fraction profile, minimizing assumptions regarding brush structure, while only allowing physically reasonable profiles to be produced. The model allows the total volume of polymer and the profile monotonicity to be constrained. The rigor of the approach is demonstrated via a round-trip analysis of a simulated system, before it is applied to real data examining the well characterized collapse of a thermoresponsive brush. It is shown that, while failure to constrain the interfacial volume and consider multimodality may result in erroneous structures being derived, carefully constraining the model allows for robust determination of polymer brush compositional profiles. This work highlights that an appropriate combination of flexibility and constraint must be used with polymer brush systems to ensure the veracity of the analysis. The code used in this analysis is provided, enabling the reproduction of the results and the application of the method to similar problems.


Soft Matter ◽  
2015 ◽  
Vol 11 (16) ◽  
pp. 3139-3148 ◽  
Author(s):  
Aykut Erbaş ◽  
Jarosław Paturej

Friction between ring polymer brush bilayers sliding past each other is studied using extensive coarse-grained molecular dynamics simulations and scaling arguments, and the results are compared to the friction between bilayers of linear polymer brushes.


1995 ◽  
Vol 385 ◽  
Author(s):  
Edith M. Sevick ◽  
Frank A. Bruce ◽  
David R.M. Williams

ABSTRACTWe describe the flow and filtration control imparted to membranes through the adsorption of polymer brushes onto the interior pores. The brushes exhibit a negative Poisson's ratio, i.e. they swell under shear, and as a result behave as sensors and valves controlling the flow and filtration through the pore. The valve-behavior of brushes adsorbed onto cylindrical pores displays the same constant discharge control but also exhibits a critical shear rate for brush swelling.


Polymers ◽  
2020 ◽  
Vol 12 (7) ◽  
pp. 1475 ◽  
Author(s):  
Kristian Birk Buhl ◽  
Asger Holm Agergaard ◽  
Mie Lillethorup ◽  
Jakob Pagh Nikolajsen ◽  
Steen Uttrup Pedersen ◽  
...  

Creating strong joints between dissimilar materials for high-performance hybrid products places high demands on modern adhesives. Traditionally, adhesion relies on the compatibility between surfaces, often requiring the use of primers and thick bonding layers to achieve stable joints. The coatings of polymer brushes enable the compatibilization of material surfaces through precise control over surface chemistry, facilitating strong adhesion through a nanometer-thin layer. Here, we give a detailed account of our research on adhesion promoted by polymer brushes along with examples from industrial applications. We discuss two fundamentally different adhesive mechanisms of polymer brushes, namely (1) physical bonding via entanglement and (2) chemical bonding. The former mechanism is demonstrated by e.g., the strong bonding between poly(methyl methacrylate) (PMMA) brush coated stainless steel and bulk PMMA, while the latter is shown by e.g., the improved adhesion between silicone and titanium substrates, functionalized by a hydrosilane-modified poly(hydroxyethyl methacrylate) (PHEMA) brush. This review establishes that the clever design of polymer brushes can facilitate strong bonding between metals and various polymer materials or compatibilize fillers or nanoparticles with otherwise incompatible polymeric matrices. To realize the full potential of polymer brush functionalized materials, we discuss the progress in the synthesis of polymer brushes under ambient and scalable industrial conditions, and present recent developments in atom transfer radical polymerization for the large-scale production of brush-modified materials.


2000 ◽  
Vol 651 ◽  
Author(s):  
Jacob Klein

AbstractA model is presented for the shear (or frictional) forces Fs between two surfaces a distance D apart as they slide past each other while bearing mutually compressed polymer brushes, on the assumption that sliding takes place at the brush-brush interface. The predictions of the model for the rapid increase in Fs at increasing compressions are in reasonable agreement with experiments on polystyrene brushes immersed in toluene over two decades in Fs. At higher compressions (smaller D) the experimental shear forces increase only slowly, and diverge from the calculated ones which continue to increase rapidly; at the same time the form of the shear force response at these higher compressions reverts from a viscous-like one to a stick-slip behaviour. These observations strongly indicate that at sufficiently high compressions the plane of slip crosses over from the brush-brush interface to the polymer-solid surface.


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