Design and implementation of a lightweight online certificate validation service

A PKI (public key infrastructure) provides for a digital certificate that can identify an individual or an organization. However, the existence of a certificate is a necessary but not sufficient evidence for its validity. The PKI needs to provide applications that use certificates with the ability to validate, at the time of usage, that a certificate is still valid (not revoked). One of the two standard protocols to check the revocation status of certificates is the Online Certificate Status Protocol (OCSP). In this article, we propose an OCSP-based implementation that enhances the performance of standard OCSP. In particular, we put special emphasis on those issues that affect security and performance when the validation service is deployed in a real scenario. Finally, we provide experimental results that show that our implementation outperforms standard OCSP.     

The crack tip: a nanolab for studying confined liquids

We study the equilibrium properties of a liquid phase condensed at the nanoscale between the surfaces of a sharp crack in fused silica in a moist controlled atmosphere. The extension of the condensed phase along the fracture is measured by in situ atomic force microscopy phase imaging and it is shown to be determined by a critical distance between the opposite crack surfaces, which is an increasing function of humidity. The present technique is very promising for measuring the properties of confined liquids at the nanoscale as well as for modeling the physics and chemistry of slow crack propagation in glasses.     

Efficient discrimination of transplutonium actinides by in vivo models

Transplutonium actinides are among the heaviest elements whose macroscale chemical properties can be experimentally tested. Being scarce and hazardous, their chemistry is rather unexplored, and they have traditionally been considered a rather homogeneous group, with most of their characteristics extrapolated from lanthanide surrogates. Newly emerged applications for these elements, combined with their persistent presence in nuclear waste, however, call for a better understanding of their behavior in complex living systems. In this work, we explored the biodistribution and excretion profiles of four transplutonium actinides (²⁴⁸Cm, ²⁴⁹Bk, ²⁴⁹Cf and ²⁵³Es) in a small animal model, and evaluated their in vivo sequestration and decorporation by two therapeutic chelators, diethylenetriamine pentaacetic acid and 3,4,3-LI(1,2-HOPO). Notably, the organ deposition patterns of those transplutonium actinides were element-dependent, particularly in the liver and skeleton, where lower atomic number radionuclides showed up to 7-fold larger liver/skeleton accumulation ratios. Nevertheless, the metal content in multiple organs was significantly decreased for all tested actinides, particularly in the liver, after administering the therapeutic agent 3,4,3-LI(1,2-HOPO) post-contamination. Lastly, the systematic comparison of the radionuclide biodistributions showed discernibly element-dependent organ depositions, which may provide insights into design rules for new bio-inspired chelating systems with high sequestration and separation performance.

Transplutonium actinides are among the heaviest elements whose macroscale chemical properties can be experimentally tested.     

Substituent Effects on Hydrogen Bonding in Watson–Crick Base Pairs. A Theoretical Study

We have theoretically analyzed Watson–Crick AT and GC base pairs in which purine C8 and/or pyrimidine C6 positions carry a substituent X = H, F, Cl or Br, using the generalized gradient approximation (GGA) of density functional theory at BP86/TZ2P. The purpose is to study the effects on structure and hydrogen bond strength if X = H is substituted by a halogen atom. Furthermore, we wish to explore the relative importance of electrostatic attraction versus orbital interaction in the above multiply hydrogen-bonded systems, using a quantitative bond energy decomposition scheme. We find that replacing X = H by a halogen atom has relatively small yet characteristic effects on hydrogen bond lengths, strengths and bonding mechanism. In general, it reduces the hydrogen-bond-accepting- and increases the hydrogen-bond-donating capabilities of a DNA base. The orbital interaction component in these hydrogen bonds is found for all substituents (X = H, F, Cl, and Br) to contribute about 41% of the attractive interactions and is thus of the same order of magnitude as the electrostatic component, which provides the remaining 59% of the attraction.     

调频广播副信道无线寻呼系统

本文主要介绍了利用调频广播附加信道实现的寻呼系统的基本原理、技术指标,并说明了该寻呼系统的优越性。     

High‐contrast homogenization of linear systems of partial differential equations

We give some integrability conditions for the coefficients of a sequence of elliptic systems with varying coefficients in order to obtain the stability for homogenization. In the case of equations, it is well known that equi‐integrability and bound in L¹ are enough for this purpose; however, this is based on the maximum principle, and then, it does not work for systems. Here, we use an extension of the Murat–Tartar div‐curl lemma because of M. Briane, J. Casado‐Díaz, and F. Murat in order to obtain the stability by homogenization for systems uniformly elliptic, with bounded coefficients in , with N the dimension of the space. We also show that a weaker ellipticity condition can be assumed, but then, we need a stronger integrability for the coefficients. Copyright © 2016 John Wiley & Sons, Ltd.