Polymer nanocomposites, nanoparticle-containing organogels utilized in forming the polymer nanocomposites, and methods for forming the polymer nanocomposites and nanoparticle-containing organogels are disclosed. Relatively simple and versatile methods are utilized to form the polymer nanocomposites. The process is based on the format of a three-dimensional network of well-individualized nanoparticles, such nanofibers through gelation thereof with an appropriate non-polymeric solvent. The nanoparticle-containing organogel is subsequently filled with a solution of a desired matrix polymer, the composite is dried and compacted to create the polymer nanocomposite. Polymer nanocomposites can be prepared which exhibit dramatic changes in mechanical properties, such as increased shear modulus, when compared to the neat polymer.
Christoph Weder - Shaker Heights OH, US Stuart J. Rowan - Cleveland Heights OH, US Jeffrey R. Capadona - North Ridgeville OH, US Dustin J. Tyler - Highland Heights OH, US Kadhiravan Shanmuganathan - Cleveland OH, US Otto van den Berg - Leuven, BE
Assignee:
Case Western Reserve University - Cleveland OH The United States of America as Represented by the Department of Veterans Affairs - Washington DC
Polymer nanocomposites exhibit a reversible change in stiffness and strength in response to a stimulus. The polymer nanocomposites include a matrix polymer with a comparably low modulus and strength and nanoparticles that have a comparably high modulus and strength. The particle-particle interactions are switched by the stimulus, to change the overall material's mechanical properties. In a preferred embodiment, a chemical regulator is used to facilitate changes of the mechanical properties. Methods for inducing modulus changes in polymer nanocomposites are also disclosed.
Eric Baer - Cleveland Heights OH, US P. Hiltner - Cleveland OH, US Christoph Weder - Shaker Heights OH, US
International Classification:
G03C001/73
US Classification:
430/290000
Abstract:
Light-reflecting multilayer polymer films that irreversibly change their optical characteristics upon exposure to suitable, high-intensity irradiation.
Embodiments of the present invention are directed toward a photoluminescent article comprising at least one host material and at least one color tunable photoluminescent dye. In certain embodiments, the emission spectrum of the at least one tunable photoluminescent dye may be dependent on the supramolecular architecture of the material. The photoluminescent emission spectrum of the dye is capable of being shifted by subjecting the article to an external stimuli such as, but not limited to, a mechanical deformation, a temperature change, aging of the article, a pressure change, exposure to a chemical compound. In specific embodiments, the color tunable photoluminescent dye is an oligo(phenylene vinylene) compound, such as, but not limited to, 1,4-Bis-(α-cyano-4-methoxystyryl)-benzene, 1,4-bis-(α-cyano-4-methoxystyryl)-2,5-dimethoxybenzene, and 1,4-bis-(α-cyano-4-(2-ethylhexyloxystyryl)-2,5-dimethoxybenzene and 2,5-bis-(α-cyano-4-methoxystyryl)-thiophene. A further embodiment of the invention is method of determining a degree of mechanical deformation, a temperature change, aging of the article, a pressure change, exposure to a chemical compound on an article.
Christoph Weder - Shaker Heights OH, US Maki Kinami - Shiga, JP Brent Crenshaw - Cleveland Heights OH, US
International Classification:
G02F 1/361
US Classification:
252582000, 524205000
Abstract:
Time temperature indicators are disclosed which comprise at least one carrier material and one aggregachromic indicator dye and which respond to the combined effects of temperature and time with an easily measurable, time-temperature dependent, irreversible, color change. The invention also discloses to methods to produce such time-temperature indicators and materials therefore. Also, the devices disclose methods for determining the time/temperature history.
Christoph Weder - Shaker Heights OH, US Stuart J. Rowan - Cleveland Heights OH, US Jeffrey R. Capadona - North Ridgeville OH, US Dustin J. Tyler - Highland Heights OH, US Kadhiravan Shanmuganathan - Cleveland OH, US Otto van den Berg - Grembergen, BE
Assignee:
The United States Government as Represented by the Department of Veterans Affairs - Washington DC CASE WESTERN RESERVE UNIVERSITY - Cleveland OH
International Classification:
C08L 1/00
US Classification:
524 35
Abstract:
Polymer nanocomposites exhibit a reversible change in stiffness and strength in response to a stimulus. The polymer nanocomposites include a matrix polymer with a comparably low modulus and strength and nanoparticles that have a comparably high modulus and strength. The particle-particle interactions are switched by the stimulus, to change the overall material's mechanical properties. In a preferred embodiment, a chemical regulator Is used to facilitate changes of the mechanical properties. Methods for inducing modulus changes in polymer nanocomposites are also disclosed.
Isbn (Books And Publications)
Poly(arylene ethynylene)s: From Synthesis To Application
Although the new generation of coatings is often called self-healing, most of these materials dont actually heal themselves, said Christoph Weder, a polymer scientist at the University of Fribourg in Switzerland. Instead, something is required to stimulate healing. Early generation versions requi
Date: Mar 26, 2012
Category: Sci/Tech
Source: Google
Maserati's Expensive Scratches May Be Fixed With Self-Repairing Material
You can think about different ways to realize thistechnology, including in a car wash, Christoph Weder,director and chair of polymer chemistry and materials at theUniversity of Fribourgs Adolphe Merkle Institute, said on thecall. While, or before, or after your car is being washed, thesyste