Biodegradable and bioactive porous polymer/inorganic composite scaffolds for bone tissue engineering

It is now widely accepted that skin sensitivity will be very important for future robots used by humans in daily life for housekeeping and entertainment purposes Despite this fact, relatively little progress has been made in the field of pressure recognition compared to the areas of sight and voice recognition, mainly because good artificial “electronic skin” with a large area and mechanical flexibility is not yet available The fabrication of a sensitive skin consisting of thousands of pressure sensors would require a flexible switching matrix that cannot be realized with present silicon-based electronics Organic field-effect transistors can substitute for such conventional electronics because organic circuits are inherently flexible and potentially ultralow in cost even for a large area Thus, integration of organic transistors and rubber pressure sensors, both of which can be produced by low-cost processing technology such as large-area printing technology, will provide an ideal solution to realize a practical artificial skin, whose feasibility has been demonstrated in this paper Pressure images have been taken by flexible active matrix drivers with organic transistors whose mobility reaches as high as 14 cm2/V·s The device is electrically functional even when it is wrapped around a cylindrical bar with a 2-mm radius

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A large-area, flexible pressure sensor matrix with organic field-effect transistors for artificial skin applications

Lignocellulosic biomass: a sustainable platform for the production of bio-based chemicals and polymers

Keywords: Fragmentation Chain-Transfer ; Self-Assembled Monolayers ; Walled Carbon Nanotubes ; Well-Defined Polymer ; Nitroxide-Mediated Polymerization ; Block-Copolymer Brushes ; Poly(Methyl Methacrylate) Brushes ; Transfer Raft Polymerization ; Quartz-Crystal Microbalance ; Poly(Acrylic Acid) Brushes Reference EPFL-REVIEW-148464doi:10.1021/cr900045aView record in Web of Science Record created on 2010-04-23, modified on 2017-05-10

Polymer Brushes via Surface-Initiated Controlled Radical Polymerization: Synthesis, Characterization, Properties, and Applications

Polydimethylsiloxane (PDMS) elastomers are extensively used for soft lithographic replication of microstructures in microfluidic and micro-engineering applications. Elastomeric microstructures are commonly required to fulfil an explicit mechanical role and accordingly their mechanical properties can critically affect device performance. The mechanical properties of elastomers are known to vary with both curing and operational temperatures. However, even for the elastomer most commonly employed in microfluidic applications, Sylgard 184, only a very limited range of data exists regarding the variation in mechanical properties of bulk PDMS with curing temperature. We report an investigation of the variation in the mechanical properties of bulk Sylgard 184 with curing temperature, over the range 25 ◦ C to 200 ◦ C. PDMS samples for tensile and compressive testing were fabricated according to ASTM standards. Data obtained indicates variation in mechanical properties due to curing temperature for Young’s modulus of 1.32‐2.97 MPa, ultimate tensile strength of 3.51‐7.65 MPa, compressive modulus of 117.8‐186.9 MPa and ultimate compressive strength of 28.4‐51.7 GPa in a range up to 40% strain and hardness of 44‐54 ShA.

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Mechanical characterization of bulk Sylgard 184 for microfluidics and microengineering

Polymers are the compounds that includes platics, artificial fibers, rubber, cellulose, and many other materials, including coatings and adhesives. This book presents key data on approximately 200 important polymers currently in industrial use or under study in industrial or academic research. No other single source covers so many polymers or offers such a depth of data. The book standardizes and makes accessible a wealth of essential data for students, teachers, researchers, and other professionals in chemistry and chemical engineering.

James E. Mark

Papers

Polymer Data Handbook