Performance enhancement of the power penalty in DWDM FSO communication using DPPM and OOK modulation

This paper presents the design and performance enhancement of the power penalty (PP) in a dense wavelength division multiplexing based on free space optical communication (FSOC) link using digital pulse position modulation (DPPM) and on–off keying (OOK) modulation. Such a system has a high performance, low cost, robust and power efficient, reliable, excessive flexibility, and higher data rate for access networks. The system performance is evaluated for an 8-channel wavelength-division-multiplexing for hybrid fiber FSOC system at 2.5 Gbps on widely accepted modulation schemes under various atmospheric turbulence (AT) regimes conditions. The performance of system is introduced in terms of PP, bit-error rate (BER), transmission distance and the average received optical power. The numerical results shows that the improvement of the PP using DPPM modulation of 0.2–3.0 dB for weak turbulence (WT) regimes for BER of 10^?6 and above 20, 25 dB for strong turbulence (ST) regimes are reported for BER of 10^?6 and 10^?9, as respectively (depending on the AT level). Further, we develop of improvement the PP caused by multiple-access interference about 6.686 dB which is predicted for target BER of 10^?9 in WT and 1 dB at target BER of 10^?6 in ST when the 8 user are active on the system of optical network units. Additionally, the optical power budget and margin losses of a system are calculated with different link length. The proposed approach of DPPM merges superiority with higher enhancement of PP about 0.8 dB for BER equal 10^?9 at FSO link length l_fso?=?2000 m compared to OOK at 1 dB for WT. An improvement of 2 dB is observed using the DPPM scheme over an OOK due to capability of detect pulses under background noise conditions with increased receiver sensitivity.     

Matrix Heterogeneity Effects on Gas Transport and Adsorption in Coalbed and Shale Gas Reservoirs

In coalbeds and shales, gas transport and storage are important for accurate prediction of production rates and for the consideration of subsurface greenhouse gas sequestration. They involve coupled fluid phenomena in porous medium including viscous flow, diffusive transport, and adsorption. Standard approach to describe gas–matrix interactions is deterministic and neglects the effects of local spatial heterogeneities in porosity and material content of the matrix. In this study, adopting weak-noise and mean-field approximations and using a statistical approach in spectral domain, matrix heterogeneity effects are investigated in the presence of non-equilibrium adsorption with random partition coefficient. It is found that the local heterogeneities can generate non-trivial transport and kinetic effects which retard gas release from the matrix and influence the ultimate gas recovery adversely. Macro-transport shows 1/[1 + N _Pe /(1 + N _Pe )] dependence on the Péclet number, and persists at the diffusive ultra-low permeability limit. Macro-kinetics is directly related to Thiele modulus by the following expression: N _Th /(1 + 2N _Pe ). It leads to trapping of gas in the adsorbed phase during its release from the matrix, and to an adsorption threshold during the gas uptake by the matrix. Both effects are proportional to the initially available adsorbed gas amount and becomes more pronounced with the increasing variance of the porosity field. Consequently, a new upscaled deterministic gas mass balance is proposed for practical purposes. Numerical results are presented showing free and adsorbed gas distributions and fractional gas sorption curves for unipore coal matrix exhibiting Gaussian porosity distribution. This study is a unique approach for our further understanding of the coalbeds and gas shales, and it is important for the development of sound numerical gas production and sequestration models.     

Determination of vanadium in serum by pre-irradiation and post-irradiation chemistry and neutron activation analysis

Vanadium in serum was investigated by pre-irradiation chemistry neutron activation analysis employing anion exchange chromatography and post-irradiation neutron activation employing solvent extraction techniques. From a comparison of these techniques it is concluded that vanadium is present in human serum in the sub-ppb range.     

A New Approach for Optimization of Distributed Quantum Circuits

International Journal of Theoretical Physics - In the present work, a novel approach was proposed to optimize the teleportation cost in Distributed Quantum Circuits (DQCs) by applying a new...     

Atom transfer radical polymerization of methyl methacrylate using copper-based homogeneous and heterogeneous catalysts

This study aimed at polymerization of methyl methacrylate with novel catalysts in the atom transfer radical polymerization (ATRP) condition at 90 °C. This was accomplished using CuBr/N-(2-aminoethyl)-3-aminopropyltrimethoxysilane (CuBr–AEAPTMS) as a homogeneous catalyst and one time with CuBr@AEAPTMS/SBA-15 as a heterogeneous catalyst. Catalysts were characterized using TGA, FT-IR, and UV–Vis spectroscopy. The structural analysis of the polymer was carried out by ¹³C NMR spectroscopy and GPC. Three characteristic parts of polymer produced by ATRP method including the initiator, monomer units, and end group was shown in ¹³C NMR spectra. In addition, the presence of C–Br unit showed that the polymerization process is alive. The ¹H NMR analysis was used for kinetic investigation of methyl methacrylate polymerization with homogeneous and heterogeneous catalysts that showed high monomer conversion (98 and 90% after 35 min, respectively) and good control of molecular weight with a dispersity (Р= 1.5–1.7). In addition, the plot of ln ([monomer]₀/[monomer] _t ) versus time gave linear relationships indicating a constant concentration of the propagating species throughout the polymerization. Finally, the results of the polymerization using heterogeneous catalyst compared with homogeneous catalyst revealed that it was according to ATRP method.     

Annihilator Conditions on Polynomials over Modules

Let R be a ring with unity and M be a right R-module. The system M[x] forms a left near R[x]-module under addition and substitution operations. In this paper we extend the study of annihilator conditions on nearring of polynomials to left near R[x]-module M[x], when M is a reduced Baer module. Also, we give a characterization of reduced modules. As a corollary we obtain some results of Birkenmeier and Huang [3].     

Cluster Model Analysis of Pion Elastic and Inelastic Scattering from 12C

Angular distributions of differential cross sections for the ¹²C(π ^±, π ^±)¹²C and ¹²C(π ^±, π ^±)¹²C^* reactions at pion kinetic energy ranging from 50 to 260 MeV have been analyzed with the 3α-particle model of ¹²C. The model provides good fits to a wide range of data. Differential cross sections for inelastic transitions to the (2^?+?; 4.44 MeV) and (3^???; 9.64 MeV) states in ¹²C are computed and the deformation lengths δ ₂ and δ ₃ are extracted. It is found that the extracted deformation lengths are sensitive to the nuclear model used and similar to the corresponding values found with other probes and nuclear models.     

ZL-amenability and characters for the restricted direct products of finite groups

Let G   be a restricted direct product of finite groups _{Gi}i∈I${\{G_i\}}_{i\in I}$, and let Z?¹(G)${\mathrm{Z}?}^1(G)$ denote the centre of its group algebra. We show that Z?¹(G)${\mathrm{Z}?}^1(G)$ is amenable if and only if _Gi$G_i$ is abelian for all but finitely many i  , and characterize the maximal ideals of Z?¹(G)${\mathrm{Z}?}^1(G)$ which have bounded approximate identities. We also study when an algebra character of Z?¹(G)${\mathrm{Z}?}^1(G)$ belongs to _c0$c_0$ or ?^p${?}^p$ and provide a variety of examples.     

Role of Zr4+ cations in NO2 adsorption on Ce(1-x)Zr(x)O2 mixed oxides at ambient conditions

Mixed oxides Ce(1-x)Zr(x)O(2) prepared by slow coprecipitation in NaOH were tested for NO(2) adsorption in dynamic conditions at room temperature. The samples were characterized before and after exposure to NO(2) by XRD, N(2)-adsorption, thermal analysis, potentiometric titration, and FT-IR. Mixed oxides show a better NO(2) adsorption capacity than the parent materials (CeO(2) and Zr(OH)(4)). This effect is linked to the presence of reduced cerium and oxygen vacancies induced by the addition of Zr(4+) cations to the structure. The results indicate that NO(2) reacts with Ce(3+) to form nitrite and nitrate species on the surface. The NO retention increases with an increase in the Zr(OH)(4) content. A decrease in the density of -OH groups on the surface after the exposure to NO(2), suggests their involvement in reactive adsorption of NO and/or NO(2). From the structural point of view, no real difference was observed on the Ce(1-x)Zr(x)O(2) materials before and after exposure to NO(2).