Preparation and Properties of PBXs Based on FOX-7 in Controlled Fragmentation Warhead Application（英）

Polymer bonded explosive(PBX)formulations were successfully prepared in the laboratory scale containing 1,1-diamino-2,2-dinitroethene(FOX-7)and hexogen(RDX)as brisant high explosives and different binder types of polyurethane(PU)based on glycidyl azide polymer(GAP) and hydroxyl-terminated polybutadiene(HTPB) as an energetic and inert polymeric binder respectively.Casting technique was used for the preparation of different PBX formulations based on FOX-7/RDX and PU(GAP/HTPB)with 14% binder.The sensitivity to different initial impulses and performance characteristics of the explosive and lethal zone of the tested controlled fragmentation warhead by the fragmentation warhead assessment test(arena test)were studied,in which the arena test was carried out with a controlled fragmentation warhead made from Ck45 steel,with dimensions(100 mm length,30 mm outer diameter and 3 mm thickness).Results show that PBXGF4 has lower sensitivity to impact and heat than those of PBXGR4 by 188.4% and 3.2% respectively.Its friction sensitivity is the same as that of PBXGR4.It has better performance,in which detonation velocity increases by 2.1% and brisance increases by 0.5% when compared with those of PBXGR4.It was concluded that PBXGF4 which based on FOX-7 bonded with PU/GAP matrix has good characteristics as PBX,specially in the sensitivity to impact and can be applied for replacing PBXs based on RDX in the advanced PBXs for low sensitive fragmentation warheads.     

Varying Electron Cyclotron Resonance Heating on the Levitated Dipole Experiment

Plasmas in the Levitated Dipole Experiment (LDX) are formed and sustained currently via two electron cyclotron resonance heating (ECRH) sources: 2.5 kW at 2.45 GHz and 2.5 kW at 6.4 GHz. An important topic being investigated is how varying the ECRH affects the confinement and stability of the plasma. We report the results of using different operational combinations of our RF sources, such as varying the power composition, changing the power levels, and sequencing of the onset time.     

Multi-objective topology optimization of multi-component continuum structures via a Kriging-interpolated level set approach

This paper explores a framework for topology optimization of multi-component sheet metal structures, such as those often used in the automotive industry. The primary reason for having multiple components in a structure is to reduce the manufacturing cost, which can become prohibitively expensive otherwise. Having a multi-component structure necessitates re-joining, which often comes at sacrifices in the assembly cost, weight and structural performance. The problem of designing a multi-component structure is thus posed in a multi-objective framework. Approaches to solve the problem may be classified into single and two stage approaches. Two-stage approaches start by focusing solely on structural performance in order to obtain optimal monolithic (single piece) designs, and then the decomposition into multiple components is considered without changing the base topology (identical to the monolithic design). Single-stage approaches simultaneously attempt to optimize both the base topology and its decomposition. Decomposition is an inherently discrete problem, and as such, non-gradient methods are needed for single-stage and second stage of two-stage approaches. This paper adopts an implicit formulation (level-sets) of the design variables, which significantly reduces the number of design variables needed in either single or two stage approaches. The number of design variables in the formulation is independent from the meshing size, which enables application of non-gradient methods to realistic designs. Test results of a short cantilever and an L-shaped bracket studies show reasonable success of both single and two stage approaches, with each approach having different merits.     

A smart multi-user massive MIMO system for next G Wireless communications using evolutionary optimized antenna selection

Recently multiserver queues with setup times have been extensively studied because they have applications in power-saving data centers. A challenging model is the M/M/c/Setup queue where a server is turned off when it is idle and is turned on if there are some waiting jobs. Recently, Gandhi et al. (in: Proceedings of the ACM SIGMETRICS, pp. 153–166, ACM, 2013; Queueing Syst. 77(2):177–209, 2014) obtain the generating function of the number of jobs in the system, as well as the Laplace transform of the response time using the recursive renewal reward approach and the distributional Little’s law (Keilson and Servi in Oper Res Lett 7(5):223– 227, 1988). In this paper, we derive exact solutions for the joint stationary queue length distribution of the same model using two alternative methodologies: generating function approach and matrix analytic method. The generating function approach yields exact closed form expressions for the joint stationary queue length distribution and the conditional decomposition formula. On the other hand, the matrix analytic approach leads to an exact recursive algorithm to calculate the joint stationary distribution and performance measures so as to provide some application insights.     

MoV-based catalysts in ethane oxidation to acetic acid: Influence of additives on redox chemistry

The formation of acetic acid and/or ethylene by oxidation of ethane is strongly dependent on X additives or Y promotor added to MoVO-based catalysts. MoV_0.4X_0.12YO_z (X = Nb; Y = Pd;  = 10⁻⁴) catalysts were prepared by the slurry method and their structural properties were studied by in situ (redox conditions) XRD, Raman and XPS techniques. The reactivity during reduction and reoxidation was analysed by thermal analysis (TGA/DSC). The oxidation of ethane was carried out in a conventional fixed bed microreactor with on line analysis by gas chromatography. Results show that Nb exerts mainly a structural effect as it is responsible for the stabilisation of molybdenum (VI) by formation of solid solutions with V, and that Pd modifies the rate of reduction of the solid catalysts. The increase of selectivity to acetic acid observed by Pd promotion is likely due to the transformation of ethylene to acetic acid occurring on neighboring Pd–V active sites.     

Simultaneous polarographic determination of isoniazid and rifampicin by differential pulse polarography method and support vector regression

A differential pulse polarography (DPP) for the simultaneous determination of isoniazid and rifampicin was proposed. Under optimum experimental conditions (pH = 7, scan rate = 10 mV/s, pulse amplitude = −50 mV), serious overlapping polarographic peaks were observed in the mixture of these compounds. In this study, support vector regression (SVR) was applied to modeling the overlapped polarograms. Furthermore, a comparison was made between the performance of SVR and partial least square (PLS) on data set. The experimental calibration matrix was designed with 30 mixtures of these compounds. Calibration graphs were linear in the range of 6 × 10⁻⁸-10⁻⁴ and 10⁻⁷-10⁻⁴ M for isoniazid and rifampicin, respectively. The results demonstrated that SVR is a good well-performing alternative for the analysis and modeling of DPP data than the commonly applied PLS technique.     

The thermal conductivity of oils sands

Measurements have been made of the effective thermal conductivity of some samples of Athabasca oil sands using a steady state method over the temperature range 20°C – 120°C. The bitumen content of the samples was altered from its natural value by mixing with additional sand and the resulting values of the thermal conductivity were found to increase with increasing the oil content. Moreover, the effective thermal conductivity values were found to decrease with increasing temperature.     

Spinodal clustering induced dewetting and non-monotonic stabilization of polymer blend films at high nanofiller concentrations

We examine the effects of high fullerene nanoparticle (f-NP) concentrations, ?_f-NP ∼ (10–20) mass% on polystyrene (PS)/polybutadiene (PB) blend thin film stability. Dewetting of the polymer blend around spinodally clustered f-NPs in this high concentration limit leads to a spinodal like dewetting morphology. This is in contrast to our previously observed results on the stabilization effects of f-NPs on PS/PB blend thin films in the intermediate f-NP concentration range of 7–10 mass%, wherein, after saturating the polymer–blend interface, the NPs stabilize the film by segregating to the blend–substrate interface. We determine three regimes of polymer blend film stability as a function of filler concentration: a) ?_f-NP < 7 mass% where preferential segregation of the f-NPs to the polymer–polymer interface leads to macroscopic dewetting, b) ?_f-NP ∼ (7–10) mass% where PS/PB blend films exhibit complete film stability, and c) ?_f-NP ∼ (11–20) mass%, where spinodal clustering of the f-NPs gives rise to polymer–NP phase exclusion and subsequent dewetting.