Adaptive synchronization and lag synchronization of uncertain dynamical system with time delay based on parameter identification

In this paper, the adaptive synchronization and lag synchronization are considered for uncertain dynamical system with time delay based on parameter identification and a novel control method is then further given using the Lyapunov functional method. With this new and effective method, parameter identification and lag synchronization can be achieved simultaneously. Simulation results are given to justify the theoretical analysis in this paper.     

Influence of aramid fiber moisture regain during atmospheric plasma treatment on aging of treatment effects on surface wettability and bonding strength to epoxy

One of the main differences between a low-pressure plasma treatment and an atmospheric pressure plasma treatment is that in atmosphere, the substrate material may absorb significant amount of water which may potentially influence the plasma treatment effects. This paper investigates how the moisture absorbed by aramid fibers during the atmospheric pressure plasma treatment influences the aging behavior of the modified surfaces. Kevlar 49 fibers with different moisture regains (MR) (0.5, 3.5 and 5.5%, respectively) are treated with atmospheric pressure plasma jet (APPJ) with helium as the carrier gas and oxygen as the treatment gas. Surface wettability and chemical compositions, and interfacial shear strengths (IFSS) to epoxy for the aramid fibers in all groups are determined using water contact angle measurements, X-ray photoelectron spectroscopy (XPS), and micro-bond pull out tests, respectively. Immediately after the plasma treatment, the treated fibers have substantially lower water contact angles, higher surface oxygen and nitrogen contents, and larger IFSS to epoxy than those of the control group. At the end of 30 day aging period, the fibers treated with 5.5% moisture regain had a lower water contact angle and more polar groups on the fiber surface, leading to 75% improvement of IFSS over the control fibers, while those for the 0.5 and 3.5% moisture regain groups were only 30%.     

Use of elemental size distributions in identifying particle formation modes

The chemical composition of particles generated during pulverized coal combustion is the consequence of their formation processes. This work aims to use the size resolved elemental composition of coal-derived particles to identify their formation modes. A size-classified bituminous coal is burnt in a laboratory drop tube furnace at 1150, 1250, and 1350 °C, respectively. The elemental composition of the size-segregated particles from coal combustion is analyzed and the total mass fraction size distributions of Si and Al are obtained. Three particle formation modes are observed in these distribution profiles. The coarse mode has the highest value of the total mass fraction of Si and Al while the ultrafine mode has the lowest one. The total mass fraction of Si and Al in these two modes is nearly independent of particle size. It is believed that the coarse mode is formed by the mineral coalescence mechanism and the ultrafine mode by the vaporization–condensation mechanism. The difference in the total mass fraction of Si and Al between the central mode and the other two indicates that the central mode is formed by different mechanisms. Based on the observation that the total mass fraction of Si and Al in this mode increases with increasing particle size, heterogeneous condensation of vaporized species on existing fine residual ash particles is proposed to account for the formation of these particles. The study of the elemental composition of the three modes represented in five categories verifies the proposed formation mechanisms for them to some extent.     

Construction of the elliptic Gaudin system based on Lie algebra

Gaudin model is a very important integrable model in both quantum field theory and condensed matter physics. The integrability of Gaudin models is related to classical r-matrices of simple Lie algebras and semi-simple Lie algebra. Since most of the constructions of Gaudin models works concerned mainly on rational and trigonometric Gaudin algebras or just in a particular Lie algebra as an alternative to the matrix entry calculations often presented, in this paper we give our calculations in terms of a basis of the typical Lie algebra, A _n , B _n , C _n , D _n , and we calculate a classical r-matrix for the elliptic Gaudin system with spin.      

Scheme for entanglement concentration of unknown W class states via linear optics

This paper proposes a scheme for entanglement concentration of unknown triparticle W class states with a certain probability. This protocol is mainly based on the coincidences of single-photon detectors and requires single-photon detectors and linear optical elements. The scheme is feasible within current technology.     

The fluorescence of polyamidoamine dendrimers peripherally modified with 1,8-naphthalimide groups: Effect of the rare earth ions and protons

We report the absorption spectra, fluorescent spectra and photophysical properties of G 2.0 polyamidoamine dendrimers with peripheral 1,8-naphthalimide groups with the hydrogen ions, the rare earth ions (Er³⁺, Tb³⁺, Nb³⁺, Eu³⁺, Yb³⁺ and Gd³⁺) and the mixture of the rare earth metal and hydrogen ions. The presence of the rare earth ions and hydrogen ions was found to enhance the fluorescence owing to the coordination between the rare earth metal or hydrogen ions and internal amido groups of polyamidoamine (PAMAM) from dendrimer. The result from the 3D isogram of the fluorescence spectra for the dendrimers with peripheral 1,8-naphthalimide groups show that it was obtained for the different emission fluorescence intensity and scope by varying the excitation wavelength and the different rare earth ions as well as its concentration. The results obtained reveal that the capacities of these systems might have acted as a sensitive label agent of the rare earth cations and protons.     

Efficient polymer white-light-emitting diodes with a single-emission layer of fluorescent polymer blend

Efficient polymer white-light-emitting diodes (WPLEDs) have been fabricated with a single layer of fluorescent polymer blend. The device structure consists of ITO/PEDOT/PVK/emissive layer/Ba/Al. The emissive layer is a blend of poly(9,9-dioctylfluorene) (PFO), phenyl-substituted PPV derivative (P-PPV) and a copolymer of 9,9-dioctylfluorene and 4,7-di(4-hexylthien-2-yl)-2,1,3-benzothiadiazole (PFO-DHTBT), which, respectively, emits blue, green and red light. The emission of pure and efficient white light was implemented by tuning the blend weight ratio of PFO: P-PPV: PFO-DHTBT to 96:4:0.4. The maximum current efficiency and luminance are, respectively, 7.6 cd/A at 6.7 V and 11930 cd/m² at 11.2 V. The CIE coordinates of white-light emission were stable with the drive voltages.     

Improvement of a low pH antigen-antibody dissociation procedure for ELISA measurement of circulating anti-Aβ antibodies

Background  

Prior work from our group found that acid dissociation (pH 2.5 incubation) of serum from APP transgenic mice vaccinated against Aβ increased the apparent anti-Aβ titers, suggesting antibody masking by antigen in the ELISA assay. Subsequently, we found that pH 2.5 incubation of serum from unvaccinated non-transgenic mice showed antibody binding to Aβ1–42, but no increase when other proteins, including shorter Aβ peptides, coated the ELISA plate. To investigate further the effects of low pH incubation on apparent anti-Aβ1–42 signals, we examined normal sera from nonTg unvaccinated mice, nonTg mice vaccinated with Aβ peptide (to produce authentic anti-Aβ antibodies) or a monoclonal antibody against Aβ (6E10) using competitive-inhibition ELISA and Aβ epitope mapping assays. In addition, we examined use of a less stringent low pH procedure at pH 3.5, to ascertain if it had the same effects as the pH 2.5 procedure.     

Donor–acceptor (donor) polymers with differently conjugated side groups at the acceptor units for photovoltaics

Four new donor–acceptor (donor) [D–A(D)], PBDT‐PTQ, PBDT‐PTTQ, PBDT‐TQ, and PBDT‐TTQ, bearing the same backbone of alternative benzodithiophene (BDT) and quinoxaline units but with phenylene thienyl, phenylene di‐thienyl, thienyl and di‐thienyl groups (other donors), respectively, at the acceptor quinoxaline units, were designed and synthesized to investigate the impacts of the conjugated side chains at the acceptor units on the photovoltaic properties of polymers. The power conversion efficiencies (PCEs) of the polymer solar cells (PSCs) based on PBDT‐TQ:[6,6]‐phenyl‐C‐70‐butyric acid methyl ester (PC70BM) and PBDT‐PTQ:PC70BM reach to 4.39 and 3.58%, respectively, which are 43 and 17% higher, respectively, than that of a reported alkylphenyl substituted polymer with the same main chain. However, the PCEs based on PBDT‐TTQ and PBDT‐PTTQ, in which an additional thiophene is added at a side chain of PBDT‐TQ and PBDT‐PTQ, respectively, decline. The mechanism how the conjugated side chains affect the performance of the PSCs is also discussed. © 2013 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013