Privacy protection vs. utility in visual data

Multimedia Tools and Applications - Ubiquitous and networked sensors impose a huge challenge for privacy protection which has become an emerging problem of modern society. Protecting the privacy of...     

[2.2]Paracyclophane-Based TCN-201 Analogs as GluN2A-Selective NMDA Receptor Antagonists

Recent studies have shown the involvement of GluN2A subunit-containing NMDA receptors in various neurological and pathological disorders. In the X-ray crystal structure, TCN-201 ( 1 ) and analogous pyrazine derivatives 2 and 3 adopt a U-shape (hairpin) conformation within the binding site formed by the ligand binding domains of the GluN1 and GluN2A subunits. In order to mimic the resulting π/π-interactions of two aromatic rings in the binding site, a [2.2]paracyclophane system was designed to lock these aromatic rings in a parallel orientation. Acylation of [2.2]paracyclophane ( 5 ) with oxalyl chloride and chloroacetyl chloride and subsequent transformations led to the oxalamide 7 , triazole 10 and benzamides 12 . The GluN2A inhibitory activities of the paracyclophane derivatives were tested with two-electrode voltage clamp electrophysiology using Xenopus laevis oocytes expressing selectively functional NMDA receptors with GluN2A subunit. The o-iodobenzamide 12 b with the highest similarity to TCN-201 showed the highest GuN2A inhibitory activity of this series of compounds. At a concentration of 10 μM, 12 b reached 36 % of the inhibitory activity of TCN-201 ( 1 ). This result indicates that the [2.2]paracyclophane system is well accepted by the TCN-201 binding site.     

BioPACE

While developing the specifications for electronically enabled Machine Readable Travel Documents, the ICAO paid significant attention to security aspects related to the digital information stored in this type of electronic document. This has resulted in Passive and Active Authentication, Basic Access Control and Extended Access Control. The goal of Basic Access Control (BAC) is preventing unauthorized access to the chip data stored on eMRTDs. The PACE protocol has been developed as a future-proof method to overcome the limitations of BAC and to replace BAC in the future. In this paper the BioPACE protocol is proposed as a supplement to the PACE protocol. Besides verifying if the document holder is indeed the rightful owner, the BioPACE protocol provides a higher convenience for the bearer of the document.     

Solar water splitting with p-SiC film on p-Si: Photoelectrochemical behavior and XPS characterization

The electrochemical properties of single-crystalline p-type 3C-SiC films on p-Si substrate were investigated as an electrode in H₂SO₄ aqueous solutions in dark and under white light illumination. The photoelectrochemical (PEC) measurements indicates the p-type 3C-SiC film on p-Si substrate can generate a cathodic photocurrent as a photocathode, which corresponds to hydrogen production, and generate an anodic photocurrent as a photoanode, which corresponds to oxygen evolution. The surface chemical states of the films were investigated by XPS. In order to observe the surface chemical state changes after PEC test, the range of applied potential to the electrode was divided into three zones: −3.6 to 0 V, 0–1.5 V and 1.5–4 V vs. Ag/AgCl. After separated PEC tests in these three areas, XPS shows the surface of the SiC film in the range of −3.6 to 0 V and 0–1.5 V was stable without oxidation except the band bending occurred. But in the range of 1.5–4 V the film surface was oxidized due to anodic oxidation.     

Flammability of layered silicate epoxy nanocomposites combined with low‐melting inorganic ceepree glass

Tetraphenylphosphonium modified layered silicate epoxy nanocomposite (EP/TPPMMT) combined with low‐melting silicate glass, Ceepree (CP) is investigated by thermal analysis, flammability tests and cone calorimeter at different heat fluxes. Adding CP and TPPMMT does not change the pyrolysis apart from increasing inorganic residue. The total heat evolved (THE) is changed insignificantly, as neither relevant additional carbonaceous charring nor flame inhibition occurs. However, flame retardancy is clearly observed due to an inorganic‐carbonaceous surface protection layer. The peak heat released rate (PHRR) is reduced by around 32–42% when 5 wt% TPPMMT is added, and 51–63% when 10 wt% CP is added. PHRR reduction less than expected is observed when both additives are combined. The reduction is greater than that achieved by using TPPMMT but less than when only CP is used. The morphology of fire residue is investigated by scanning electron microscope on different length scales and turns out to be the key to understanding the efficiency of flame retardancy. The fire residue of EP/CP shows a layered structure, whereas separated columns limit the barrier properties for EP/5%TPPMMT on the micrometer scale. Columns dominating the fire residue structure of EP/5%TPPMMT/10%CP deteriorate the fire retardancy, whereas a more integral structure at the top of the residue causes the improvement over EP/5%TPPMMT. POLYM. ENG. SCI., 2012. © 2011 Society of Plastics Engineers