31,959 research outputs found
Three methods for in situ cross-linking of polyvinyl alcohol films for application as ion-conducting membranes in potassium hydroxide electrolyte
Three methods of in situ cross-linking polyvinyl alcohol films are presented. They are: (1) acetalization with a dialdehyde such as glutaraldehyde, (2) acetalization with aldehyde groups formed by selective oxidative cleaving of the few percent of 1,2 diol units present in polyvinyl alcohol, and (3) cross-linking by hydrogen abstraction by reaction with hydrogen atoms and hydroxyl radicals from irradiated water. For the third method, improvement in film conductivity in KOH solution at the expense of mechanical strength is obtained by the presence of polyacrylic acid in the polyvinyl alcohol films. Resistivities in 45 percent KOH are given for in situ cross-linked films prepared by each of the three methods
In-situ cross linking of polyvinyl alcohol
A method of producing a crosslinked polyvinyl alcohol structure, such as a battery separator membrane or electrode envelope is described. An aqueous solution of a film-forming polyvinyl alcohol is admixed with an aldehyde crosslinking agent a basic pH to inhibit crosslinking. The crosslinking agent, perferably a dialdehyde such as glutaraldehyde, is used in an amount of from about 1/2 to about 20% of the theoretical amount required to crosslink all of the hydroxyl groups of the polymer. The aqueous admixture is formed into a desired physical shape, such as by casting a sheet of the solution. The sheet is then dried to form a self-supporting film. Crosslinking is then effected by immersing the film in aqueous acid solution. The resultant product has excellent properties for use as a battery separator
In situ self cross-linking of polyvinyl alcohol battery separators
A battery separator was produced from a polyvinyl alcohol sheet structure which was subjected to an in situ, self crosslinking process by selective oxidation of the 1,2 diol units present in the polyvinyl alcohol sheet structure. The 1,2 diol units were cleaved to form aldehyde end groups which subsequently crosslink through acetalization of the 1,3 diol units of the polyvinyl alcohol. Selective oxidation was achieved using a solution of a suitable oxidizing agent such as periodic acid or lead tetraacetate
Cross-linked polyvinyl alcohol and method of making same
A film-forming polyvinyl alcohol polymer is mixed with a polyaldehyde-polysaccharide cross-linking agent having at least two monosaccharide units and a plurality of aldehyde groups per molecule, perferably an average of at least one aldehyde group per monosaccharide units. The cross-linking agent, such as a polydialdehyde starch, is used in an amount of about 2.5 to 20% of the theoretical amount required to cross-link all of the available hydroxyl groups of the polyvinyl alcohol polymer. Reaction between the polymer and cross-linking agent is effected in aqueous acidic solution to produce the cross-linked polymer. The polymer product has low electrical resistivity and other properties rendering it suitable for making separators for alkaline batteries
Sagnac Interferometer Enhanced Particle Tracking in Optical Tweezers
A setup is proposed to enhance tracking of very small particles, by using
optical tweezers embedded within a Sagnac interferometer. The achievable
signal-to-noise ratio is shown to be enhanced over that for a standard optical
tweezers setup. The enhancement factor increases asymptotically as the
interferometer visibility approaches 100%, but is capped at a maximum given by
the ratio of the trapping field intensity to the detector saturation threshold.
For an achievable visibility of 99%, the signal-to-noise ratio is enhanced by a
factor of 200, and the minimum trackable particle size is 2.4 times smaller
than without the interferometer
Method of cross-linking polyvinyl alcohol and other water soluble resins
A self supporting sheet structure comprising a water soluble, noncrosslinked polymer such as polyvinyl alcohol which is capable of being crosslinked by reaction with hydrogen atom radicals and hydroxyl molecule radicals is contacted with an aqueous solution having a pH of less than 8 and containing a dissolved salt in an amount sufficient to prevent substantial dissolution of the noncrosslinked polymer in the aqueous solution. The aqueous solution is then irradiated with ionizing radiation to form hydrogen atom radicals and hydroxyl molecule radicals and the irradiation is continued for a time sufficient to effect crosslinking of the water soluble polymer to produce a water insoluble polymer sheet structure. The method has particular application in the production of battery separators and electrode envelopes for alkaline batteries
Alkaline battery containing a separator of a cross-linked copolymer of vinyl alcohol and unsaturated carboxylic acid
A battery separator for an alkaline battery is described. The separator comprises a cross linked copolymer of vinyl alcohol units and unsaturated carboxylic acid units. The cross linked copolymer is insoluble in water, has excellent zincate diffusion and oxygen gas barrier properties and a low electrical resistivity. Cross linking with a polyaldehyde cross linking agent is preferred
How Much Does Money Matter in a Direct Democracy?
The fine-structure splitting of quantum confined InxGa1-x Nexcitons is investigated using polarization-sensitive photoluminescence spectroscopy. The majority of the studied emission lines exhibits mutually orthogonal fine-structure components split by 100-340 mu eV, as measured from the cleaved edge of the sample. The exciton and the biexciton reveal identical magnitudes but reversed sign of the energy splitting.Original Publication:Supaluck Amloy, Y T Chen, K F Karlsson, K H Chen, H C Hsu, C L Hsiao, L C Chen and Per-Olof Holtz, Polarization-resolved fine-structure splitting of zero-dimensional InxGa1-xN excitons, 2011, PHYSICAL REVIEW B, (83), 20, 201307.http://dx.doi.org/10.1103/PhysRevB.83.201307Copyright: American Physical Societyhttp://www.aps.org
Work in progress: Data explorer - Assessment data integration, analytics, and visualization for STEM education research
Citation: Weese, J. L., & Hsu, W. H. (2016). Work in progress: Data explorer - Assessment data integration, analytics, and visualization for STEM education research.We describe a comprehensive system for comparative evaluation of uploaded and preprocessed data in physics education research with applicability to standardized assessments for discipline-based education research, especially in science, technology, mathematics, and engineering. Views are provided for inspection of aggregate statistics about student scores, comparison over time within one course, or comparison across multiple years. The design of this system includes a search facility for retrieving anonymized data from classes similar to the uploader's own. These visualizations include tracking of student performance on a range of standardized assessments. These assessments can be viewed as pre- and post-tests with comparative statistics (e.g., normalized gain), decomposed by answer in the case of multiple-choice questions, and manipulated using pre-specified data transformations such as aggregation and refinement (drill down and roll up). Furthermore, the system is designed to incorporate a scalable framework for machine learning-based analytics, including clustering and similarity-based retrieval, time series prediction, and probabilistic reasoning. © American Society for Engineering Education, 2016
Unitarity and the Hilbert space of quantum gravity
Under the premises that physics is unitary and black hole evaporation is
complete (no remnants, no topology change), there must exist a one-to-one
correspondence between states on future null and timelike infinity and on any
earlier spacelike Cauchy surface (e.g., slices preceding the formation of the
hole). We show that these requirements exclude a large set of semiclassical
spacetime configurations from the Hilbert space of quantum gravity. In
particular, the highest entropy configurations, which account for almost all of
the volume of semiclassical phase space, would not have quantum counterparts,
i.e. would not correspond to allowed states in a quantum theory of gravity.Comment: 7 pages, 3 figures, revtex; minor changes in v2 (version published in
Class. Quant. Grav.
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